EFFECTS OF ANTHROPOGENIC DISTURBANCE
ON THE DIVERSITY OF FOLIICOLOUS LICHENS IN
TROPICAL RAINFORESTS OF EAST AFRICA:
GODERE (ETHIOPIA), BUDONGO (UGANDA)
AND KAKAMEGA (KENYA)
Dissertation
Zur Erlangung des akademischen Grades eines
Doktors der Naturwissenschaft
Fachbereich 3: Mathematik/Naturwissenschaften
Universität Koblenz-Landau
Vorgelegt
am 23. Mai 2008
von Kumelachew Yeshitela
geb. am 11. April 1965 in Äthiopien
Referent: Prof. Dr. Eberhard Fischer
Korreferent: Prof. Dr. Emanuël Sérusiaux
In Memory of
my late mother Bekelech Cheru
i
Table of Contents
Abstract……………………………………………………………………………….......…...iii
Chapter 1. GENERAL INTRODUCTION.................................................................................1
1.1 Tropical Rainforests ......................................................................................................... 1
1.2 Foliicolous lichens............................................................................................................ 5
1.3 Objectives ......................................................................................................................... 8
Chapter 2. GENERAL METHODOLOGY.............................................................................. 10
2.1 Foliicolous lichen sampling............................................................................................ 10
2.2 Foliicolous lichen identification .....................................................................................10
2.3 Data Analysis.................................................................................................................. 12
Chapter 3 DIVERSITY OF FOLIICOLOUS LICHENS IN GODERE FOREST,
ETHIOPIA.............................................................................................................. 22
3.1 Study area ....................................................................................................................... 22
3.2 Study sites....................................................................................................................... 30
3.3 Results ............................................................................................................................ 31
3.4 Discussion....................................................................................................................... 51
3.5 Conclusion...................................................................................................................... 55
Chapter 4 DIVERSITY OF FOLIICOLOUS LICHENS IN BUDONGO FOREST,
UGANDA...............................................................................................................56
4.1 Study area ....................................................................................................................... 56
4.2 Study sites....................................................................................................................... 68
4.3. Results ........................................................................................................................... 69
4.4 Discussion....................................................................................................................... 91
4.5 Conclusion...................................................................................................................... 94
Chapter 5. DIVERSITY OF FOLIICOLOUS LICHENS IN KAKAMEGA FOREST,
KENYA .................................................................................................................. 95
5.1 Study area ....................................................................................................................... 95
5.2 Study sites.................................................................................................................... 110
5.3 Results .......................................................................................................................... 114
5.4 Discussion..................................................................................................................... 140
5.5 Conclusion.................................................................................................................... 144
Chapter 6. DIVERSITY OF FOLIICOLOUS LICHENS ALONG DISTURBANCE
GRADIENT: A COMPARATIVE ANALYSIS OF GODERE, BUDONGO
AND KAKAMEGA FORESTS ...........................................................................145
6.1 Introduction .................................................................................................................. 145
6.2 Study area ..................................................................................................................... 146
6.3 Methodology................................................................................................................. 149
6.4 Results .......................................................................................................................... 150
6.5 Discussion..................................................................................................................... 164
6.6 Conclusion.................................................................................................................... 171
References .......................................................................................................................... 173
Appendices ......................................................................................................................... 197
Acknowledgments .................................................................................................................. 263
ii
Abstract
Foliicolous lichens are one of the most abundant epiphytes in tropical rainforests
and one of the few groups of organisms that characterize these forests. Tropical
rainforests are increasingly affected by anthropogenic disturbance resulting in
forest destruction and degradation. However, not much is known on the effects of
anthropogenic disturbance on the diversity of foliicolous lichens. Understanding
such effects is crucial for the development of appropriate measures for the
conservation of such organisms.
In this study, foliicolous lichens diversity was investigated in three tropical
rainforests in East Africa. Godere Forest in Southwest Ethiopia is a transitional
rainforest with a mixture of Afromontane and Guineo-Congolian species. The forest
is secondary and has been affected by shifting cultivation, semi-forest coffee
management and commercial coffee plantation. Budongo Forest in West Uganda is
a Guineo-Congolian rainforest consisting of primary and secondary forests.
Kakamega Forest in western Kenya is a transitional rainforest with a mixture of
Guineo-Congolian and Afromontane species. The forest is a mosaic of nearprimary forest, secondary forests of different seral stages, grasslands, plantations,
and natural glades.
Leaves carrying foliicolous lichens were collected from the forest understorey in the
shady understorey and light gap microsite regimes. Morphological and anatomical
characters were used for the identification of foliicolous lichens. Different indices
were used for the computation of α- and β-diversity. The biogeographical
distribution patterns of the foliicolous lichens of the study area and the possible use
of foliicolous lichens as indicator of forest disturbance were analysed.
A total of 70 species of foliicolous lichens and lichenicolous fungi belonging to 27
genera and 15 families were recorded from Godere Forest. From Budongo Forest
125 species of foliicolous lichens & lichenicolous lichens belonging to 32 genera
and 16 families were recorded. From Kakamega Forest 137 species belonging to
41 genera and 17 families were recorded. In addition, 7 foliicolous lichens new to
science have been recorded in this study. The most species-rich families in both
forests were Pilocarpaceae, Porinaceae, Gomphillaceae, and Strigulaceae.
iii
In Godere higher foliicolous lichen diversity was recorded in Dushi than in Bishan
Waka forest site. In Budongo high foliicolous lichen diversity was recorded in the
young secondary and the primary swamp forests. In Kakamega Forest high
foliicolous lichen diversity was recorded in the sites of Yala, Buyangu, Isiukhu, and
Kisere. Low diversity was recorded in Malava, Kaimosi and Camp site. Among the
3 forests investigated, α-diversity was significantly higher in Kakamega and
Budongo than in Godere forest. β-diversity was high in Kakamega and Budongo
and low in Godere. Several studies have shown higher foliicolous lichen diversity in
undisturbed primary forests than in disturbed secondary forests. Our study showed
high foliicolous lichen diversity in both primary forest and secondary forests with
little disturbance. Therefore, for the maintenance of high foliicolous lichen diversity
in tropical Africa both primary and old growth forests should be conserved.
This study has shown that foliicolous lichens are good indicators of forest
disturbance. The composition of foliicolous differed from primary to secondary and
disturbed forests. In addition, some foliicolous lichens were found to be restricted to
a particular forest type. The distribution of forest sites along PCA ordination axis
has been found to depend on the level of disturbance. Based on the distribution of
species and forest sites on the PCA ordination biplot, indicator species for three
forest
types
with
different
disturbance
regimes
were
selected.
Porina
sphaerocephala, P. conica, P. radiate and Mazosia rotula were found to have high
fidelity to undisturbed or slightly disturbed closed forets. Coenogonium geralense,
C. siquirrense, C. pocsii and Byssoloma leucoblepharum were identified as
indicators of closed forest with moderate disturbance. Asterothyrium rotuliforme,
Psorotheciopsis gyalideoides, P. varieseptata, Calenia aspidota and Gyalectidium
imperfectum were found to be indicators of disturbed semi-open forests.
Biogeographic affinity of the foliicolous lichens of the study area shows that 57% of
the species have pantropical distribution, 18.6% of the species are restricted to the
African paleotropics, 17% of the species are distributed both in the African
paleotropics and the Neotropics, and 7.2% of the species are distributed both in the
African and Eastern paleotropics. In addition 13 species which have not been
recorded from Africa have for the first time been recorded in this study.
iv
General Introduction
Chapter 1. GENERAL INTRODUCTION
1.1 Tropical Rainforests
1.1.1 Extents and uses
Tropical rainforests are Earth’s most complex ecosystem in terms of both
structure and species diversity. They are composed of evergreen broadleaved
trees which flourish in the high temperature and humidity of the low altitudes
between 100 north and 100 south of the equator (Park 1992). Although tropical
rainforests cover only 6% of Earth's land surface, they harbour roughly half of all
the world's plant and animal species (National Research Council 1992).
Tropical rainforests are found in Central and South America, Southeast Asia and
Central and Western Africa. The tropical rainforests of Latin America harbours 56
percent of the world total, Southeast Asia harbours 25 percent and Central and
West Africa harbour 18 percent (Park 1992, Whitmore 1998).
According to the review made by Richards (1996), the large mass of rainforest in
Africa is found in the Congo basin from where it continues westwards into Gabon
and Cameroon. From there a narrow belt follows the coast of the Gulf of Guinea
through Nigeria to Ghana and beyond, finally ending in Guinea at about 100N. This
western extension of the rainforest is interrupted from western Nigeria to a little
west of the Volta River in Ghana by Dahomey Gap, where savannas reach the sea
and divide the forest into an eastern and a western block. South of the Democratic
Republic of Congo, the African rainforest extends into Angola to about 90S. In East
Africa the area of continuous forest reaches its eastern limit at Bwamba in western
Uganda. East of the Western Rift Valley, forest similar to tropical rainforest is
absent except for outliers of various sizes, e.g. Budongo Forest and fragments near
Lake Victoria in Uganda, a relic near Kakamega in western Kenya and some small
areas in northwestern Tanzania.
The tropical rainforests of Africa are the most species-riche ecosystem in the region
housing more than half of Africa’s biota (Sayer et al. 1992). They are estimated to
contain over 8000 plant species, some 80 % of which are endemic (White, 1983).
1
General Introduction
The total forest cover in Africa is estimated at 635,412,000 ha, accounting for 21 %
of the land area and 16 % of global forest cover (FAO, 2006).
Tropical forests provide environmental, economical and aesthetic services and
values. They provide row materials for plant improvement programs and modern
pharmaceutical industries. They regulate local and global climate and play
important role in watershed management, soil erosion control and the carbon
dioxide budget of global atmosphere. Millions of people living in or around tropical
forests depend on the forests for many forest products and environmental services.
Tropical forests are the main source of energy in the form of fuelwood; they provide
timber and non-timber forest products; they are sources of food, particularly in
times of drought and famine; and they are sources of traditional medicines.
1.1.2 Deforestation and fragmentation in tropical forests
Human activity has had devastating impacts on tropical forests. Human impact
could be in the form of conversion of natural forest into other land uses
(deforestation), fragmentation into smaller patches with deforested areas in
between, and various degrees of disturbance, such as silvicultural activities.
Deforestation is the permanent loss of forest to other land uses such as agriculture,
grazing, new settlements, and infrastructure. Deforestation in the tropics is widely
recognized as one of the main environmental problems facing the world today.
Tropical forests are being destroyed and fragmented at an ever-increasing rate with
series environmental and biological consequences including loss of biodiversity
(Whitmore & Sayer 1994, Turner 1996) and climate change at local, regional and
global levels (Myers 1988). The Food and Agriculture Organization of the United
Nations (FAO 2006) estimated that in the 1990s tropical countries have lost
111,350 km2 of forests annually and 114,270 km2 of tropical forests were lost
between 2000 and 2005.
The forests of Africa have long been affected by humans. Outside the Congo core
the African rainforests have been extensively destroyed (Whitmore 1998). The
estimate for the annual rates of deforestation in Africa is 43,750 km2 for the period
1990-2000 and 40,400 km2 for 2000-2005 (FAO 2006). In East Africa the forest
2
General Introduction
resources are steadily disappearing and those that are left are being degraded.
Between 1990 and 2000 the forest covers of Ethiopia, Uganda and Kenya were
respectively reduced from 49,960 km2 to 45,930 km2, from 51,030 km2 to 41,900
km2 and from 180,270 km2 to 170,960 km2 (FAO 2001). Most of the remaining
forests in these countries today exist as disturbed and secondary forests of different
seral stages.
One major consequence of deforestation is the fragmentation of habitats in natural
forests. Habitat fragmentation is the subdivision of continuous habitat blocks into
clusters of small remnant patches isolated by matrix of other land use types
(Andrén 1994, Fahrig 2003). Fragmentation could occur by natural disturbance
(e.g. fire, windthrow) or due to anthropogenic disturbance which include clearing of
forest for agriculture, road and dam construction and logging (Attiwill 1994, Wade et
al. 2006).
Habitat fragmentation causes changes in the physical environment and
biogeographic entities (Saunders et al. 1990). Loss and fragmentation of natural
habitat are considered major threats to global biodiversity (Lovett & Wasser 1993,
Laurance & Bierregaard 1997). The effect is more severe in tropical forests where
diversity is high and forests are being removed and fragmented at an increasing
rate (Pineda & Halffter 2004).
Forest fragmentation has impact on biodiversity (Turner 1996), increasing isolation
of habitats, endangering species of plants, mammals and birds (Skole & Tucker
1993, Scariot 1999, Laurance et al. 2000) and on a variety of population and
community dynamic processes (Saunders et al. 1991, Valladares et al. 2006).
However, the effects of habitat fragmentation on species diversity vary among
different habitats and taxa. These effects could be both positive and negative
(Fahrig 2003). Positive effects include the creation of edge habitat increasing the
abundances of edge or gap species (Yahner 1988, Malcom 1994) and negative
impacts include increasing the local rate of extinction by reducing population sizes
(Leach & Givnish 1996), creating forest edges and altering microclimate at forest
edges (Matlack 1993), changing forest dynamics (Wade et al. 2006), and
increasing predation at forest edges (Chalfoun et al. 2002). These impacts may be
due to one or a combination of four separate effects: forest fragmentation per se,
3
General Introduction
the loss of habitat during fragmentation, habitat degradation following the isolation
of fragments, and the effect of isolation per se (Harrison & Bruna 1999). Some
ecologists (Fahrig 1997, Caley et al. 2001, Fahrig 2003) advocate the separation of
habitat loss and habitat fragmentation per se and claim that species loss and
decline in species abundance following fragmentation is associated with habitat
loss than with fragmentation per se (Caley et al. 2001).
Although there are various studies on the impact of habitat fragmentation on
bryophytes (Zartman 2003), lichens (Esseen & Renhorn 1998), palms (Fleury
2006), beetles (Davies & Margules 1998), butterflies ( Daily & Ehrlich 1995), corals
(Caley et al. 2001), amphibians (Pineda 2003), birds (Hagen et al. 1996, Carlson
2001, Githiru & Lens 2007, Giraudo et al. 2008) and mammals (Laurance 1994,
Malcolm 1997), the long-term effect of habitat fragmentation on species diversity is
far from being known.
The major causes of forest destruction and degradation in the tropical Africa are
conversion to subsistence and commercial agricultural land use, fuelwood
collection, human settlement, commercial logging, and overgrazing by domestic
animals. These causes are driven and aggravated by poverty and population
growth. Most of the people in tropical Africa live in rural area and the rate of
population growth in these areas is high (e.g. > 2.5% in East Africa, Masci 2006).
The increasing population growth demands additional land for agriculture which in
most cases can only be met by forest conversion. Migration and settlement of
landless people from densely populated and draught affected parts to areas
covered by forest in search of agricultural land and to engage in charcoal
production and pit sawing to sell for the rapidly growing urban centers has also
accelerated the rate of deforestation. Development policies outside the forestry
sector have contributed for the destruction of forests in many African countries. The
conversion of natural forests into commercial plantations such as coffee and tea
plantations in Ethiopia (Yeshitela 2001), sugarcane plantation in Uganda and
sugarcane and tea plantations in Kenya are some of the examples.
4
General Introduction
1.2 Foliicolous lichens
Santesson (1952) defined foliicolous lichens as those growing on living leaves of
vascular plants. Ecologically, foliicolous lichens could be grouped into three groups.
Typical foliicolous lichens grow and reproduce entirely on leaves. Facultative
foliicolous lichens grow on barks, petioles and twigs but exceptionally grow on
leaves. Ubiquitous species equally grow and reproduce on living leaves and twigs.
In addition, foliicolous lichens have been observed growing on artificial substrates
such as plastics materials (Sipman 1994, Lücking 1998c, Sanders 2002, Sanders &
Lücking 2002, Sanders 2005).
Foliicolous lichens are found in tropical forests of central and south America, Africa
and Southeast Asia. They are one of the most abundant epiphytes in tropical
rainforests (Richards 1996, Lücking 2001, Anthony et al. 2002) and one of the few
groups of organisms that characterize these forests (Lücking 2001). Outside the
tropical areas, foliicolous lichens are found in subtropical areas (Vězda 1983,
Sérusiaux 1993, 1996, Puntillo & Ottonello 1997, Puntillo et al. 2000, Thor et al.
2000, Llop & Gómez-Bolea 2006) and temperate rainforests (Malcolm & Galloway
1997, Lücking et al. 2003), but then occurrence is very limited and restricted to very
humid areas.
After the monographic work of Santesson (1952) on obligately foliicolous lichens,
there has been a considerable study on the taxonomy, distribution and even
phylogeny of foliicolous lichens and several publications, including revisions and
monographs, have been produced. Several new taxa have been described and the
taxonomy of already described taxa has been amended. Compared to corticolous
microlichens of tropical forests, the taxonomy, diversity and distribution of
foliicolous lichens is well understood.
The checklist of foliicolous lichens and lichenicolous lichens (Lücking et al. 2000a)
listed 716 species and 72 genera of foliicolous lichens. Since then many foliicolous
lichens have been described, among others, by Ferraro et al. (2001), Lücking &
Kalb (2001), Lücking & Lumbsch (2001), Lücking & Santesson (2001), Lücking et
al. (2001), Sérusiaux & Lücking (2001), Herrera-Campos & Lücking (2002, 2003),
Lücking & Kalb (2002), Lücking & Santesson (2002), Ferraro & Lücking (2003),
5
General Introduction
Lücking et al. (2003), Sérusiaux & Lücking (2003), Herrera-Campos et al. (2004a),
Vezda (2004), Lücking et al. (2006), Lücking (2006), Rivas-Plata et al. (2006),
Lücking et al. (2007), Papong et al. (2007), Sérusiaux (2007), Sérusiaux & Lücking
(2007) and Lücking (2008)
Foliicolous lichens exhibit structural diversity of growth form, thallus, ascomata and
conidiomata. All foliicolous lichens are crustose except members of the genera
Coccocarpia,
Leptogium,
Parmeliella
and
Psoroma
which
assume
foliose/squamulose growth habit. Growth could be supracuticular (most follicolous
lichens) or subcuticular (e.g. Strigula antillarum, S. nemathora, S. smaragdula),
epiphyllous (most foliicolous lichens) or hypophyllous (Coenogonium hypophyllous,
Strigula janeirensis, Bacidina hypophylla).
Thallus could be smooth (e.g. Coengonium pocsii, Porina rubentior) or verrucose
(e.g. Mazosia melanopthalma, Porina mazosioides, Sporopodium leprieurii) or
farinose-granulose (Bacidina sp.), corticate (e.g. species of Asterothyrium, and
Psorotheciopsis and Calenia bullatinoides) or ecorticate (most follicolous lichens);
with hairs (e.g. species of Aderkomyces, Tricharia, and Rubrotricha) or with out
hairs (most foliicolous lichens); dispersed (e.g. species of Loflammia, and
Tapellaria major) or continuous (e.g. Strigula macrocarpa).
Mycobiont could be ascomycetes (most foliicolous lichens), or basidiomycetes
(Dictyonema sp.). Phycobiont could be Trentepohlia sp. (e.g. Coenogonium sp.),
Phycopeltis (e.g. Porina epiphylla), Cephaleuros (e.g. species of Strigula) or
Trebouxia sp. (e.g. Sporopodium leprieurii).
Ascomata could be apothecia (e.g. species of Fellhanera, Chroodiscus), or
perithecia (e.g. species of Porina and Strigula). Ascomata could occur singly (most
foliicolous lichens) or within stromata (e.g. Flavobathelim epiphyllum). Conidiomata
could be pycnidia (e.g. Coenogonium subluteum, Fellhanera africana, Caprettia
setifera), campylidia (e.g. Musaespora kalbii, species of Sporopodium, Calopadia,
Tapllaria, and Badimia) or hyphophores (species of Gomphillaceae).
Vegetative
Coccocarpia
propagation
could
domingensis,
be
with isidia
Phylloblastia
(e.g.
borhidii,
Chroodiscus
Porina
distans,
mirificus,
Bacidina
6
General Introduction
scutellifera, Coenogonium isidiiferum), or soredia (e.g. Fellhanera ivoriensis,
Bapalmuia napoensis).
The diversity and distribution of foliicolous lichens is influenced by geographical
distribution and environmental factors. Generally foliicolous lichens diversity is high
in tropical regions, usually close to the equator (Herrera-Campos et al. 2004b) and
species richness decreases with increasing latitudes. Altitudinal zonation of
vegetation, degree of seasonality and microclimatic condition of light intensity are
the most important factors (Lücking 1992b, Lücking 1995, Lücking 1997d). Species
richness is highest at low altitude forests and decreases at high altitude forests
(Herrera-Campos et al. 2004b). Diversity decreases with increasing seasonality
where synchronized leaf shading becomes a hindrance for foliicolous lichens
establishment, growth and reproduction (Lücking 1997d). Therefore, diversity is
high in the wet, humid or moist forests in which a dry season is absent or is slight
and decreases as the length of dry season increases. Within a tropical rainforest,
diversity is high in the shady understorey and decreases in the light gap and the
upper canopy. Not only is there a change in diversity along microclimatic gradient,
but also differences in species composition. In tropical rain forest, for example,
species of the family Arthoniaceae, Porinaceae and supra-cuticular Strigulaceae
dominate in the shady understorey, in the light gap species of Gomphillaceae, subcuticular Strigulaceae and campylidia bearing members of the Pilocarpaceae
dominate and members of the Asterothyriaceae and Gomphillaceae dominate in
the canopy (Cáceres et al. 2000, Lücking 2001).
In tropical rainforests, foliicolous lichens exhibit broad phorophyte ranges and low
specificity (Aptroot 1997, Lücking 1998b). They exhibit phorophyte preference only
in species poor sites of subtropical forests (Conran 1997). The principal features of
the phorophytes that govern species richness of foliicolous lichens are leaf surface
structure, leaf longevity and presence or absence of hairs (Lücking 1998e). Species
richness is high on phorophytes having long-lived leaves with grooved or
ornamented fine surface and high surface continuity. Hairs or glands on the upper
leaf surface influence the growth of foliicolous lichens by influencing air and water
currents on leaf surface (Lücking 1998e), thus rendering the successful
establishment of diaspores more difficult.
7
General Introduction
Lichens are poikilohydric organisms lacking mechanisms for regulating uptake and
loss of water. They take water and nutrients across the surface of their body. As a
result, their growth and distribution are influenced by microenvironmental features
of light intensity, humidity and temperature (Connelissen & Ter Steege 1989,
Renhorn et al. 1997).
Therefore, activities and events that result changes in
microhabitat could affect their diversity. Conversion of tropical rainforest into
agricultural land (Pócs 1996) and forest fragmentation (Brown & Jarman 1994) are
the biggest threat to lichens and other epiphyllous flora. Foliicolous lichens are
more vulnerable than corticolus ones as the later could survive in small niches after
destruction of the forest (Pócs 1996). Shade loving lichens with higher air moisture
requirements are affected by canopy openings and the formation of edges during
forest degradation.
As compared to tropical America and South East Asia, the foliicolous lichen flora of
tropical Africa is insufficiently known. Among the East African countries Tanzania
and Kenya are comparatively better known for their foliicolous lichens with 144
species in Tanzania (Feuerer 2007) and 97 species including 5 lichenicolous fungi
in Kenya (Lücking & Kalb 2002). Feuerer (2007) listed only 29 foliicolous lichen
species for Uganda while no foliicolous lichen species is included among the 279
lichen species list of Ethiopia. Therefore, much task is ahead before the foliicolous
lichens of tropical Africa are adequately known. However, the ongoing high rate of
deforestation is frustrating that many lichens may disappear before we discover and
name them. It is therefore high time that the foliicolous lichen diversity of primary as
well as anthropogenic forests is documented and utilized for the development of a
sustainable forest management program.
1.3 Objectives
With the current state of increasing dependence of people on forest resources,
degradation and conversion of forests in tropical Africa is not going to stop soon. It
is thus necessary to design mechanisms by which biodiversity can be conserved
and the conservation value of forests already degraded improved under conditions
of high human pressure. However, our knowledge on the biodiversity of tropical
forests is fragmentary and many groups of organisms, including cryptogams, are
8
General Introduction
unknown or inadequately known. It is therefore necessary to study diversity in
primary forests as well as the impact of human exploitation on biodiversity.
1. The phanerogamic flora of Godere, Budongo and Kakamega forests are
comparatively well known. However, there is no information on the cryptogamic
flora the area. Therefore, the first objective of the present study is to describe
the foliicolous lichen flora of these forests.
2. Anthropogenic disturbances affect the biodiversity of an area and the response
of organisms to such disturbances is variable. Therefore, in this study
•
the effects of forest disturbance on the diversity of foliicolous lichens is
evaluated
•
the change in the diversity of foliicolous lichens along forest disturbance
gradient is analyzed
3. For a sustainable forest management, emphasis should be given to the
conservation of forest biodiversity. For this to happen, the current status of
biodiversity should be known and assessed. In this regard, the importance of
foliicolous lichens as bioindicators of particular forest types and disturbance
levels is evaluated.
4. Foliicolous lichens have different geographic distribution patterns. In this regard,
the lichenogeographical distribution of the foliicolous lichens of the study area is
evaluated.
This study is part of the multidisciplinary research project ‘BIOTA East Africa:
Conservation and sustainable use of East African rainforest ecosystems’ financed
by the German Ministry for Research and Education.
9
General Methodology
Chapter 2. GENERAL METHODOLOGY
2.1 Foliicolous lichen sampling
Sampling for foliicolous lichens was performed following the sampling methods
outlined by Lücking & Lücking (1996). Transects were laid in a homogenous stand
of forest and phorophytes reaching a height of up to 3 m were considered for
sampling both in the shady understorey and in the light gap microsites of the
understorey vegetation. From each phorophyte individuals, a single branch with
comparatively much foliicolous lichen was selected as a sample and the leaves
that carried foliicolous lichens were collected. From Dracaena fragrans, the shoot
was considered as a sample and up to 10 leaves were collected. Leaves were
also collected from a recently fallen canopy trees. On average 633 leaves were
collected from Godere Forest, 2040 leaves from Budongo Forest and 3040 leaves
from Kakamega Forest.
Identification of specimen of foliicolous lichens was based on examination of
morphological and anatomical features. Morphological characters of thallus,
ascomata and conidiomata were examined under stereomicroscope. Hand cut
sections and squash preparations were made for studies of the anatomy of thalli
and reproductive structures, including perithecia, apothecia, campylidia, pycnidia,
and hyphophores and examined under Olympus light microscope. Luglo’s solution
was used for the color reactions of ascus walls. Photographs were taken under the
light microscope. Voucher specimens of all collections are deposited in the
herbarium of the department of Biology of the University of Koblenz-Landau
(KOBL) in Germany.
2.2 Foliicolous lichen identification
For a general identification of foliicolous lichen genera, Santesson (1952), Lücking
(1992a) and the internet key developed by Lücking (2000a) were utilized. In
addition, the following literatures were consulted for generic identification. For
genera in the Arthoniaceae Lücking (1995a) and Ferraro & Lücking (1997), for
10
General Methodology
Asterothyriaceae
Lücking
(1999b)
and
Henssen
&
Lücking
(2002),
for
Coccocarpiaceae Swinscow & Krog (1988), for Gomphillaceae Lücking et al.
(2005), for lichenicolous fungi Matzer (1996), for Pilocarpaceae (Vězda 1986), for
Porinaceae Hafellner & Kalb (1995), for Rocellaceae Grübe (1998) and Sparrius
(2004), and for Thelotremataceae Frisch (2006).
For species and infra-specific taxa identification, the following sources of
information were used. For Aderkomyces Vězda (1975a) and Lücking et al.
(2005); for Arthonia Santesson (1952), Lücking (1992a), Lücking (1995a), and
Ferraro & Lücking (1997); for Aspidothelium Sérusiaux & Lücking (2001); for
Asterothyrium Santesson (1952), Vězda (1979), Lücking (1999b), Henssen &
Lücking (2002), and Lücking & Kalb, K. (2002); for Aulaxina Vězda (1979), Lücking
(1997a), and Lücking et al. (2005); for Bacidia Ekman (1996); for Bacidina Vězda
(1980), Vězda (1990a), and Farkas & Vězda (1993); for Badimia Vězda (1980);
for Bapalmuia Santesson & Lücking (1999), and Kalb et al. (2000); for Brasilicia
Vězda (1974) and Santesson & Lücking (1999); for Byssolecania Santesson
(1952) and Lücking & Kalb (2000); for Byssoloma Santesson 1952, Vezda
(1975b), Vězda (1987), Kalb & Vězda (1990), and Lücking (1997c); for Calenia
Vězda (1979), Lücking (1997a), Lücking et al. (2001b), and Lücking et al. (2005);
for Calopadia Santesson (1952), Vězda (1986), Lücking (1997c), and Lücking
(1999c); for Caprettia Vězda (1975), Malcolm & Vězda (1995b), Sérusiaux &
Lücking (2003), and Vězda (2004); for Chroodiscus Lücking (1999b), Santesson &
Lücking (1999), and Lücking & Grube (2002); for Coccocarpia Santesson (1952),
Arvidsson (1991) and Lücking et al. (2007); for Coenogonium Vězda & Farkas
(1988), Vězda (1990b), Malcolm & Vězda (1995b), Lücking (1999a), Lücking &
Kalb (2000), and Rivas-Plata et al. (2006); for Echinoplaca Vězda (1979), Lücking
(1997a), Lücking et al. (2005); for Enterographa Herrera-Campos & Lücking
(2002), Lücking & Matzer (1996), Sparrius (2004), and Ertz et al. (2005); for
Eremothecella Sérusiaux (1992), and Lücking (1995a); for Eugeniella Sérusiaux &
Lücking (unpublished); for Fellhanera Vězda (1974), Vězda (1975), Vězda (1980),
Vězda (1986), Sérusiaux (1996), Lücking (1997b), Lücking & Santesson (2001),
and Lücking et al. (2001a); for Gyalectidium Vězda (1979), Sérusiaux & De
Sloover (1986), Lücking (1997a), Ferraro et al. (2001), and Lücking et al. (2005);
for Gyalidea Vězda (1966), Vězda (1973), Vězda (1979), Vězda & Poelt (1991),
11
General Methodology
and Henssen & Lücking (2002); for Gyalideopsis Lücking & Sérusiaux (1998), and
Lücking et al. (2006); for Lasioloma Vězda (1986), and Lücking & Sérusiaux
(2001); for Loflammia Santesson (1952), Vězda (1986), and Lücking (1999c); for
Lyromma Lücking (1992), and Lücking & Kalb (2000); for Mazosia Vězda (1973),
Farkas (1987), and Kalb & Vězda (1988a); for Musaespora Lücking & Sérusiaux
(1997); for Phylloblastia Vězda (1982), Farkas & Vězda (1993), and Lücking
(2008); for Porina Santesson (1952), Vězda (1975a), Farkas (1987), Lücking
(1991), Vězda (1994), Hafellner & Kalb (1995), Lücking (1996), Lücking & Vězda
(1998), Lücking et al. (1998), and Lücking (2004); for Psorotheciopsis Santesson
(1952), Vězda (1973), Vězda (1974), and Henssen & Lücking (2002); for
Sporopodium Santesson (1952), Vězda (1986), Elix et al. (1995), Lücking (1999c),
and Lücking & Kalb (2002); for Strigula Santesson (1952), Farkas (1987), Lücking
(1991), and Lücking (1992a); for Tapellaria Santesson (1952), Sérusiaux (1984),
and Vězda (1986); for Tricharia Vězda (1979), Lücking (1997a), Lücking et al.
(2005), and Kalb & Vězda (1988b); and for Trichothelium Lücking (1991), Malcolm
& Vězda (1995a), Lücking (1998a) and Vězda (1994).
Nomenclature follows Lücking et al. (2000) for species described until 2000 and
for species described after 2000 the most recent literature for the taxon are
followed. For species in the genus Coenogonium nomenclature follows RivasPlata et al. (2006).
2.3 Data Analysis
2.3.1 Floristic composition and species frequency
The foliicolous lichen species compositions of Godere, Budongo and Kakamega
forests as well as their respective forest types are described. Frequency which is
the number of samples in which a species occurs is computed for each forest as a
whole and the various forest types separately. The following frequency classes
were used to designate the frequency status of a species:
≤10% occurrence = Rare
11-20% occurrence =Occasional
21-30% occurrence =Less frequent
31-40% occurrence =Frequent
12
General Methodology
41-50% occurrence = Very frequent
>50% occurrence = Dominant
2.3.2 Alpha-diversity
Alpha-diversity is the diversity within a particular sample or community. It is also
called the within-habitat diversity. Direct species count to give species richness is
the simplest measure of diversity. Many diversity indices, however, take into
account two aspects of species diversity: species richness and species evenness
(equitability). Species richness describes how large the number of species in a
community is, while species evenness describes the relative abundance with
which each species is represented in an area. There are various measures of
species richness, evenness and diversity to compare communities.
2.3.2.1 Sample based rarefaction and species accumulation curves
Comparison of community samples based on different sample sizes is problematic
in the determination of species richness as the number of species observed is
dependent on the sample size (Peet 1974, Magurran 1988). To overcome this
problem, all samples from different communities should be standardized to a
common sample size of the same number of individuals (Krebs 1994). A
rarefaction method (Sanders 1968) provides a procedure to scale down all
collections to the same sample size number for comparison when the samples are
taxonomically similar and the sampling methods the same. A species
accumulation curve is the graph of the cumulative number of observed species as
a function of some measure of sampling effort (Colwell & Coddington 1994).
Sample based accumulation curves result when sampling is based on some
sampling units (e.g. quadrats) and the total number of species is accumulated as a
result of successively sampling additional sampling units (Gotelli & Colwell 2001).
Rarefaction and species accumulation curves are closely related (Magurran 2004).
Rarefaction estimates the number of species expected to be seen in a smaller
sample. The species accumulation curves are used to estimate the total number of
species.
In this study sample based rarefaction curves (Gotelli & Colwell 2001) are
computed in order to compare the species richness of different forest types in
13
General Methodology
Godere, Budongo and Kakamega forests. Species accumulation curves were
computed for the various forest types to estimate the number of species, to
examine the degree of foliicolous lichen collection, and to evaluate the
effectiveness of the species richness estimators.
2.3.2.2 Species richness estimation
The observed number of species in a given habitat is usually less than the number
of actually occurring species. There are different estimation methods that allow
estimation of the expected number of species from sample data (Colwell &
Coddington 1994, Magurran 2004). In this study non-parametric species
estimators which are appropriate for incidence-based (presence/absence) data
were followed. The estimators are Chao 2, First Order Jackknife (Jack 1), Second
Order Jackknife (Jack 2), Bootstrap, and Incidence Based Coverage Estimator
(ICE),
and
Michaelis-Menten
Means
(MMMeans).
These
non-parametric
estimators estimate species that are absent in the sample data, but likely to exist
in a larger homogenous sample, from the proportional abundances of species
within the total sample (Soberón & Llorente 1993, Chao et al. 2005)
EstimateS version 8 (Colwell 2006) which is a public domain software was used to
compute the expected species accumulation curves and estimates of the expected
species richness. The sample order was randomized 100 times to compute the
mean estimator and expected species richness for each sample accumulation
level.
The equations EstimateS uses in estimating species richness are as follows
(Colwell 2006).
1. The Chao 2 incidence-based estimator is based on the number of uniques
(species found in only one sample), and the number of duplicates (species
found in exactly two samples). The classic formula is
2
S Chao 2 = S obs +
Q1
,
2Q2
and the bias-corrected formula is
⎛ m − 1 ⎞⎛⎜ Q1 (Q1 − 1) ⎞⎟
S Chao 2 = S obs + ⎜
⎟⎜
⎟
⎝ m ⎠⎝ 2(Q2 + 1) ⎠
14
General Methodology
where Schao2 = the expected species number based on Caho 2 estimator
Sobs = the number of species observed
Q1 = the number of uniques
Q2 = the number of duplicates
m = total number of species
2. The first order Jackknife estimator is based on the number of species occurring
in only one sample.
⎛ m −1⎞
S jack 1 = S obs + Q1 ⎜
⎟
⎝ m ⎠
where Sjack1 = the expected species number based on Jack 1 estimator
Sobs = the number of species observed
Q1 = the number of uniques
m = total number of species
3. The second order Jackknife estimator is based on the number of species
occurring in only 1 sample and the number of species occurring in exactly 2
samples.
⎡ Q (2m − 3) 2 Q2 (m − 2) 2 ⎤
S jack 2 = S obs + ⎢ 1
−
⎥
m
m(m − 1) ⎦
⎣
where Sjack2 = the expected species number based on Jack 2 estimator
Sobs = the number of species observed
Q1 = the number of uniques
Q2 = the number of duplicates
m = total number of species
4. The Bootstrap estimator is based on the proportion of samples containing each
species.
S obs
S boot = S obs + ∑ (1 − p k )
m
k =1
where Sboot = the expected species number based on Bootstrap estimator
Sobs = the number of species observed
pk = proportion of samples that contain species k
m = total number of species
15
General Methodology
5. Incidence-based Coverage Estimator is based on species found in 10 or fewer
samples.
S ice = S freq +
C ice = 1 −
γ 2 ice
Q1
N inf r
S inf r
Q
+ 1 γ 2 ice
C ice C ice
,
10
N inf r = ∑ jQ j ,
j =1
10
⎡
⎤
j ( j − 1)Q j
∑
⎢S
⎥
minf r
j =1
inf r
⎢
= max
− 1,0⎥
⎥
⎢ C ice (minf r − 1) ( N inf r ) 2
⎥
⎢
⎣
⎦
where Sice = expected species number based on incidence-based coverage
estimator
Sfreq = number of frequent species (each found in more than 10 samples)
Sinfr = number of infrequent species (each found in 10 or fewer samples)
Cice = sample incidence coverage estimator
Ninfr = total number of incidences (occurrences) of infrequent species
minfr = number of samples that have at least one infrequent species
γ 2 ice = estimated coefficient of variation of the Q1 for infrequent species
6. Michaelis-Menten Mean richness estimator (MMMean) is an asymptotic
extrapolation of the species accumulation curve. It computes the estimates
once for each sample pooling level based on the species accumulation curve
as computed by MaoTau in EstimateS.
2.3.2.3 Shannon-Wiener measure of diversity
The Shannon-Wiener index (Shannon & Weaver 1949) of diversity is the most
commonly used to characterize diversity in a community. The index is based on
the rationale that the diversity or information in a natural system can be measured
in a similar way to the information contained in a code or a message (Magurran
2004). It assumes that individuals are randomly sampled from an infinitely large
16
General Methodology
community, and that all species are represented in the sample (which is always
difficult to attain in plant communities). The index has the following formula:
s
H ' = −∑ pi ln p i
i =1
pi =
ni
N
where H’= Shannon-Wiener index of species diversity (calculated with base e logs)
pi = proportion of total sample belonging to ith species
N = total number of species
ni = individual number of species i
The Shannon Diversity Index typically falls between 1.5 and 4.0, with lower values
indicating lower diversity, and higher values indicating higher diversity. The
Shannon index tends to be weighted slightly towards rare species.
2.3.2.4 Shannon’s Index of evenness
The evenness component of diversity expresses how individuals are distributed
among the species. A community with all individuals equally distributed among the
species is more diverse than a community with high dominance of one or few
species. Among the various indicies of evenness, the Shannon's evenness was
computed as the ratio of observed diversity to maximum diversity (Magurran
1988).
s
H'
J '=
=
H ' max
∑p
i
ln p i
i =1
ln s
where J’ = Equitability (evenness)
s = the number of species
pi = the proportion of individuals of the ith species
ln = log basee
17
General Methodology
2.3.3 Beta-diversity
Beta diversity or between-habitat diversity is the measure of the change in species
diversity between habitats or communities. It is usually expressed in terms of a
similarity index between communities or as a species turnover rate. In this study
the former is computed with Sørensen index of similarity for qualitative data
(Sørensen 1948) and the latter with Whittaker’s index for β-diversity (Whittaker
1960).
βw =
S
α
where βw = Whittaker’s index of diversity
S = the total number of species in a forest type
α = the mean sample species number
Ss =
2c
a+b
where Ss= Sørensen similarity index,
a = the number of species in one forest type
b= the number of species in the other forest types
c= the number of species common to both forest types
2.3.4 Statistical analysis
Statistical analysis were performed to determine whether the data are normally
distributed, to check the equality of variances of means and for the comparison of
the mean species number of samples. Levene Equal-Variance test was performed
to test the equality of variances. Shapiro-Wilk test (Shapiro & Wilk 1965) was run
in order to test for normal distribution of the species distribution of samples. When
distributions were found to be non normal, the Kruskal-Wallis Analysis of Variance
test (Kruskal & Wallis 1952) was employed for the comparison of samples. This
test is a non-parametric method for testing equality of population medians among
groups. It is most commonly used when the measurement variable does not meet
the normality assumption of an analysis of variance (ANOVA). The basic
assumptions of the Kruskal-Wallis test are independent samples, continuous
variables, a measurement scale of at least ordinal scale and the distributions for
18
General Methodology
the groups are identical (Hintze 2007). When Kruskal–Wallis test provided
significant difference, it was followed by comparisons of mean ranks using
Kruskal-Wallis multiple comparison procedures.
The values of Shannon diversity indices of the various study sites in Godere,
Budongo and Kakamega forests were compared for significant differences using ttest and ANOVA. Magurran (2004) pointed out that estimate of diversity produced
by the Shannon index is approximately normally distributed making comparisons
with parametric tests feasible. When ANOVA resulted in significant difference, it
was followed by Fischer’s least significant post hoc treatment to see which study
sites are significantly different.
For calculating the variance of the Shannon index of diversity, the following
formula given by Magurran (1988) was used.
∑ p (ln pi) − ∑ ( pi ln pi)
2
VarH ' =
i
N
2
−
S −1
2N 2
The t statistic for the t test associated with the Shannon index is
t=
H '1 − H ' 2
VarH 1 '+VarH ' 2
where VarH’ = variance of the Shannon index
N= sample size
S= No. of species
A significance probability less than p < 0.05 was considered as significant
differences between means and medians. All statistical analyses were performed
with the software NCSS (Hintze 2007) and Statigraphics version 5 software
(Statistical Graphics Corporation).
2.3.5 Multivariate analysis
Data from community ecology usually consist of the abundance or importance of
taxa (usually species) indexed by sampling units (Palmer 1993). Such data are
multidimensional and multivariate analysis is required for easy summarization of
19
General Methodology
the data. In this study an indirect gradient analysis (indirect ordination) is followed
to summarize the floristic data of the study sites. Indirect ordination is based on
analysis of floristic data with the assumption that examination of variability in
floristics reflects variation in environment (Kent & Coker 1992).
Detrended Correspondence Analysis (DCA; Hill and Gauch 1980) is an indirect
gradient analysis for ordination of samples and species. DCA is a method based
on the assumption of unimodal response of species abundance to environmental
gradient and uses weighted averaging for calculation of ordination scores. The
axes of DCA are scaled in units of the average standard deviation of species
turnover and describe gradients. The eigenvalue associated with each axis can be
thought of as the proportion of variation in sample or species dispersion explained
by that axis (Gauch 1982). DCA arranges samples according to their species
similarity along axes in a multi-dimensional space with the eigenvalue of the first
axis greater than that of the second and so on.
Principal Component Analysis (PCA) is a method that reduces data dimensionality
by performing a covariance analysis between factors. It involves a mathematical
procedure that transforms a number of (possibly) correlated variables into a
(smaller) number of uncorrelated variables called principal components. The first
principal component accounts for as much of the variability in the data as possible,
and each succeeding component accounts for as much of the remaining variability
as possible. PCA is a method based on the assumption of linear response of
species abundance to environmental gradient and uses eigenvalues to determine
axis values.
The species by sample data matrices of Godere and Budongo forests were
subject to ordination analysis by DCA as a means of summarizing the information
in the data matrices. Before subjecting the data matrices to DCA analysis,
samples with 3 and less species were removed to reduce noise resulting from rare
species. Presence/absence data were converted to quantitative value ranging
between 0 and 1 expressing the probability of a species occurrence in a sample in
relation to the other species in the sample. The resulting data matrix contained 75
species and 60 samples for Godere, 129 species and 164 samples for Budongo,
20
General Methodology
and 146 species and 304 samples for Kakamega. However, the variation
explained by the first three axes of DCA ordination of the data matrix of Kakamega
was very small (14.3% of the total variation). Therefore, for the ordination of
Kakamega’s data Principal Component Analysis was performed on the species by
forest site data matrix. PCA is preferred to DCA because the gradient length was
short (less than 3) in the initial correspondence analysis and ter Braak & Šimilauer
(2002) recommended PCA for short gradient lengths. In the DCA ordination
detrending by segment (26 segments), downweighting of rare species and log
transformation of species data were selected. In the PCA ordination centering by
species was selected. Both DCA and PCA ordinations were run using the software
CANOCO 4.5 (ter Braak & Šimilauer 2002).
21
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
Chapter 3 DIVERSITY OF FOLIICOLOUS LICHENS IN
GODERE FOREST, ETHIOPIA
3.1 Study area
3.1.1 Location and physiography
Godere Forest is situated in Godere District of the Gambella People’s National
Regional State (GPNRS) in southwestern Ethiopia between 07008.395’7023.437’N Latitude and 34°52.793’-35°25.445’E Longitude (Fig. 3.1). The forest
covers an area of 120,000 ha (Bureau of Agriculture, GPNRS, unpublished
document) and altitude in the forest varies from 500 m a.s.l. to 2400 m a.s.l. At
altitudes between 500 and 1500 m the natural forests belong to the transitional
rainforest type of Friis (1992) and the afromontane rainforest type is found at
altitudes above 1500 m. About 52 % of the forest is found at elevations between
500 and 1000 m and 38 % of the forest between 1000 and 1500 m altitude
(Ersado 2003).
At altitudes above 1250 m, the topography is characterized by undulating and
dissected terrain. At altitudes below 1250 m and the terrain becomes rather flat
and about 83 % of the forest develops on this flat terrain. Godere, Achani and Gilo
are the major rivers in the forest and belong to the Baro-Akobo drainage system
which is the tributary of the Nile River.
3.1.2. Geology and Soil
In Ethiopia, the basement complex upon which all the younger formations were
deposited contains the intensively folded and faulted Precambrian rocks (Mohr
1962, Kazmin 1972, Westphal 1975). These rocks are overlain by Mesozoic rocks,
mainly sandstone and limestone, and by Tertiary volcanic rocks, mainly basalts,
rhyolites, trachytes, tuffs, ignimbrites, agglomerates (Friis 1992). The Southwest
Ethiopia Volcanites, which include the Omo Basalts (Oligocene to Miocene) and
the Jimma Volcanites (Oligocene to Miocene), are found in southwestern Ethiopia
(Asres 1996).
22
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
There is no published information on the soils of the study area. From the general
account of the soils of southwestern Ethiopia by Asres (1996), it can be deduced
that the soils of the study area are Nitosols having a depth of more than 1.5 m. An
analysis of soil samples take from Godere Forest undertaken by the National Soil
Laboratory of the Ethiopian Institute of Agricultural Research on behalf of the
Institute of Biodiversity Conservation shows that the soil is slightly acidic (pH 6.5),
and is rich in exchangeable bases (Sodium 0.72 meq/100 g, Potassium 2.4
meq/100 gm, Calcium 22.4 meq/100 g, Magnesium 7.7 meq/100 g) and cation
exchange capacity (38.6 meq/100 g). The soils were reddish brown, well drained
and clay in texture.
Fig. 3.1 Map of Gambella Regional State in southwestern Ethiopia and the location
of Godere District
23
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
3.1.3. Climate
The climate in Ethiopia depends on the prevailing winds of the humid Southwest
Monsoon and the dry Northeast Trade Winds, which are governed by the
movement of the Inter-Tropical Convergence Zone (ITCZ), (Liljequist 1986). In the
summer (May to October), the ITCZ is north of the Equator; the prevailing wind
over most of Ethiopia is southwesterly. These moisture-laden wind-systems
produce rain over large areas of the escarpments and plateaux, the highest rainfall
being in the southwestern parts of the country (Friis 1992).
In the winter
(December to February), the ITCZ is south of the equator, the Northeast Trade
Winds influence the climate of southwestern Ethiopia resulting in a dry season.
All the highlands in southwest which are above 1000 m altitude receive an annual
rainfall of between 1400 and 2200 mm (Ayele & Al Shadily 2000). At Tepi (7005’ N,
35015’ E, 1250 m altitude), a town about 40 km from Godere Forest, the mean
annual rainfall is 1562 mm with most of the rain occurring from May to September
(Asres 1996). Average annual temperature ranges in the forest between 15 and 25
0
C.
3.1.4 Vegetation and flora
The forest vegetation of Ethiopia has been classified by various authors (Logan
1946, Chaffey 1979, Friis 1986, Friis 1992). Friis (1992) classified the forests of
Ethiopia in to seven types: lowland dry peripheral semi-deciduous GuineoCongolian forest, transitional rainforest, Afromontane rainforest, undifferentiated
Afromontane forest, dry single dominant Afromontane forest of the Ethiopian
Highlands, dry single-dominant Afromontane forest of the escarpments, and
riverine forest.
According to the classification of Friis (1992), a lowland dry peripheral semideciduous Guineo-Congolian forest, transitional rainforests, and Afromontane
rainforests are found in southwestern Ethiopia. The following description of these
forest types is based on Friis (1992).
The dry peripheral semi-deciduous Guineo-Congolian forests are restricted to the
Baro lowlands of Gambella in southwestern Ethiopia. The forests occur on well
24
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
drained sandy soils on flat area at altitudes ranging from 450-600 m a.s.l. The
mean annual maximum temperature is 35-38°C and the corresponding minimum
temperature is 18-20°C and the mean annual rainfall ranges from 1300 to 1800
mm, the rainy season being from May to September. The forest is semideciduous, with a 15-20 m tall, more or less continuous canopy of Baphia
abyssinica (endemic to the lowlands of southwestern Ethiopia and adjacent parts
of Sudan on the Boma Plateau and Mt. Tomadur) mixed with less common
species such as Celtis toka, Diospyros abyssinica, Lecaniodiscus fraxinifolius,
Malacantha alnifolia, Trichilia prieureana, Zanha golungensis, and Zanthoxylum
leprieurii. The species that emerge high above the main canopy are Alstonia
boonei, Antiaris toxicaria, Melicia excelsa, and Celtis gomphophylla. Small trees
such as Acalypha neputnica, Erythroxylum fischri, Tapura fischeri, Ziziphus
pubescens, and Xylopia parviflora form a continuous stratum below the canopy.
The shrub layer is sometimes dense and includes Alchornea laxiflora,
Argomuellera marcophylla, Mimulopsis solmsii, Oncoba spinosa, Oxyanthus
speciosus, Rinorea ilicifolia and Whitfieldia elongata. Hippocratea parvifolia, H.
goetzei, Combretum paniculatum, and Ampelocissus abyssinica are the
dominating woody climbers.
The transitional rainforests occur on the escarpments of southwestern highlands in
Bench-Maji Zone, Illubabor Zone and Godere District. The forest occurs at
altitudes between 500 and 1500 m a.s.l., partly in river valleys, partly in areas
presumed to have a high water table. The mean annual rainfall is about 2000 mm
with rain falling most of the year, the maximum being between May and
September. The mean annual temperatures range from 20 to 25°C. The
transitional rainforest is similar in physiognomy and composition to the
Afromontane rainforest of southwestern Ethiopia, with additional species from the
lowland dry peripheral semi-deciduous Guineo-Congolian forest and with few
species restricted to the transitional rainforest. The species in the latter forest type
include
Pouteria
(Aningeria)
altissima,
Anthocleista
schweinfurthii,
Campylospermum bukobense, Celtis philippensis, C. zenkeri, Croton sylvaticus,
Dracaena fragrans, Elaeodendron buchananii, Eugenia bukobensis, Ficus
exasperata, Garcinia huillensis, Manilkara butugi, Morus mesozygia, Strychnos
mitis, Trichilia dregeana, and Trilepisium madascariense.
25
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
An inventory of Godere Forest made by the Institute of Biodiversity Conservation
in 2001 has recorded 97 woody species. Awas et al. (2001) recognized Manilkara
butugi-Cordia africana community type in Godere Forest. The community type is
characterized by Manilikara butugi and Cordia africana. Other trees include
Mimusops kummel, Pouteria (Aningeria) altissima, Alchornea laxiflora, and Celtis
zenkeri. The shrubs include Justicia schimperiana, Dracaena fragrans, Whitfieldia
elongate, Argomuellera macrophylla and Acalypha acrogyna. Lianas include
Hippocratea africana and H. pallens.
The afromontane rainforests are found distributed in Illubabor, Sheka, Kefa,
Bench-Maji, and Jimma Zones in southwestern Ethiopia. The forest is found at
altitudes between 1500 and 2500 m with mean annual temperatures ranging from
18-200C and annual rainfall between 1500 and more than 2000 mm with rain most
of the year, but a maximum between April and October. Pouteria (Aningeria)
adlofi-frederici is an emergent tree in the 20-30 m high canopy. The canopy trees
include Olea capensis, Ilex mitis, Schefflera abyssinica, Ekebergia capensis,
Macaranga capensis, Euphorbia ampliphylla, Euphorbia ampliphylla, Schefflera
abyssinica, Ficus thonningii, Ocotea kenyensis, Croton macrostachyus, Albizia
schimperiana, A. gummifera, A. grandibracteata, Ficus sur. F. ovata, F. thonningii,
Prunus africana, Sapium ellipticum, Syzygium guineense, and Polyscias fulva. A
discontinuous
lower canopy of smaller trees includes Allophylus abyssinicus,
Apodytes dimidiata, Bersama abyssinica, Brucea antidysenterica, Calpurnia
aurea, Canthium oligocarpum, Chionanthus mildbraedii, Clausena anisata, Coffea
arabica, Cyathea manniana, Deinbollia kilimandscharica, Dracaena afromontana,
D. fragrans, D. steudneri, Ehretia abyssinica, Erythrina brucei, Galiniera saxifraga,
Lepidotrichilia volkensii, Milletia ferruginea (endemic to Ethiopia), Nuxia congesta,
Oncoba routledgei, Oxyanthus speciosus, Phoenix reclinata, Pittosporum
viridiflorum, Psychotria orophila, Ritchiea albersii, Rothmannia urcelliformis, Teclia
nobilis, Trema orientalis, Turraea holstii, and Vepris dainellii. Ground herbs include
Aframomum corrorima, Desmodium repandum and many grass species. Lianas
include Hippocratea goetzei, H. africana, Landolphia buchananii, Jasminium
abyssinicum, Urera hypselodendron, and Tiliacora troupinii.
26
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
3.1.5 Fauna
The fauna of the forests of southwestern Ethiopia have not been adequately
studied. Brown & Urban (1971) studied the mammals and birds of southwestern
Ethiopia including the forest in Godere and came up with a list of 48 mammals
species. Godere Forest falls under Metu-Gore-Tepi forest Important Bird Areas
(EWNHS 1996) and the area supports Afrotropical highlands biome species and
small populations of Rougetius rougetii (Rouget's Rail) and Macronyx flavicoliis
(Abyssinian Longclaw), which are classified as Globally threatend. Poicephalus
flavifrons (Yellow Fronted Parrot) and Dendropicos abyssinicus (Abyssinian
Woodpecker) are two endemic birds of Ethiopia found in the area. Species
otherwise rarely recorded in Ethiopia include Podica senegalensis, Cossypha
niveicapilla, Nectarinia chloropygia and Euplectes gierowii.
3.1.6 Management status
Natural forests in Ethiopia are administered by the regional governments. The Yeki
Forest in Yeki District and Godere Forest in Godere District were designated as
Yeki-Godere state forest in 1988. Following the separation of the regional
administration of Yeki and Godere districts, Godere Forest became a state forest
and its management and administration rested on the Gambella Peoples’ National
Regional Government.
Godere Forest is one of the 58 National Forest Priority Areas of Ethiopia
established in 1989 for conservation and production purpose. However, nothing
has been done to fulfill the articulated purposes as there were no legislations
issued to enforce management. Godere Forest lacks proper demarcation and a
forest management plan has never been prepared. The Institute of Biodiversity
Conservation with financial support from the German Technical Cooperation
undertook an inventory of woody plant diversity and socio-economic survey in
Godere and other forests in southwestern Ethiopia in order to identify priority
woody species for in situ and ex situ conservation (see Dessie 2003 & Ersado
2003). Baphia abyssinica, Malacantha alnifolia, Morus mesozygia and Celtis
zenkeri were the priority species selected from Godere Forest (Bekele et al. 2002).
27
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
3.1.7 Human Impact
Human impact in Godere Forest is seen in the form of fallow farming, commercial
logging, resettlement and coffee plantation. The lowland part of Godere Forest is
predominantly inhabited by the Mejenger ethnic group who are dependent on the
forest for their survival. The people speak Mejenger which belongs to the Nilotic
language family. Population density in Godere District is 22.7 people per square
kilo meter (CSA 2007). Traditionally, the Mejenger people were hunter gatherer
and shifting cultivator for long until they lost their forest land for the establishment
of state coffee plantation and expansion of agriculture by settlers and changed
their life style to fallow and sedentary farming and bee keeping (Tadesse 2007).
In shifting cultivation, the farmers set fire in the forest to remove trees, shrubs and
lianas and they cultivate the land for food crops for three to five years. When they
assume that the fertility of the land is declined, they abandon the land and shift to
another forest area in their surrounding to do the same. The farmers dig hole with
traditional wooden stick and plant maize, sorghum, pumpkin and beans together.
In addition, root crops like Yam (Dioscorea cayenensis), Cassava (Manihot
esculenta), and Taro (Colocasia esculenta) are planted by the Mejenger.
The natural forests of southwestern Ethiopia are the source of logs for most of the
forest industries in Ethiopia (Abebe 2003). Godere Forest is the supplier of logs for
Bebeka sawmill in Meti, a town 10 km far from Godere Forest, and other three
sawmills in the southwestern Ethiopia (Abebe & Holm 2003). Timber extraction
from Godere Forest started in 1986 (Abebe 2003). The sawmills use selective
logging and the main tree species logged were Cordia africana and Pouteria
adolfi-friederici.
Coffee production has contributed for the decline in the natural vegetation cover of
Godere Forest. Two types of coffee production system are practiced in Godere
forest area. In the semi-forest coffee production system, all small trees, shrubs
and climbers are removed while big trees are maintained to provide shade to the
coffee plant. This system is practiced by individual farmers. In the state and private
large-scale coffee plantation system, the natural forest is removed for coffee
plantation leaving only few shade trees.
28
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
For more than two decades, Godere Forest has been affected by commercial
coffee plantation by the state-owned Tepi Coffee Plantation Enterprise (TCPE)
which was established in 1988 and maintains 7082 ha of coffee plantation in the
area (Tadesse 2007). In the last decade, private investors were granted forestland
for the same purpose. As the forest is converted for coffee plantation, all shrubs,
lianas and most of the trees are removed, leaving only those trees which provide
shade for the coffee. Albizia gummifera, Millettia ferruginea and Cordia africana
are the most preferred indigenous shade trees while Gravillea robusta is an exotic
tree planted as shade tree. In addition, the construction of access roads inside the
forest, construction of residences for the staff and families of TCPE, establishment
of offices and coffee processing facilities, have resulted in the clearing of the
natural forest cover.
The employment opportunity provided by TCPE for the collection of coffee beans
has attracted many people from different parts of Ethiopia. Some of these people
do not go back home after they finish their contract with the enterprise. They rather
try to acquire forestland illegally and start cultivation. Once settled, these people
go back to their former home area to bring family members and provoke relatives
and friends to come to the forest area of Godere for settlement. As a result of
such illegal settlement, most areas of Godere Forest has been converted for
settlement, coffee plantation and food crop production.
In the mid of 1980s, the Ethiopian government carried out a large scale
resettlement program in parts of southwestern Ethiopia for people from draught
affected parts of Ethiopia. In addition to arable lands, natural forests were selected
for the resettlement program. Godere Forest was one of the forests selected for
the program. Most of these settlers came from parts of the country which practice
sedentary agriculture and where no natural forests exist. As a result vast area of
the forest had been converted to agricultural land, coffee plantation and villages.
Tadesse (2007) investigated the forest cover change in parts of southwestern
Ethiopia including Godere using satellite image analysis. The result showed that
the high forest cover of the area decreased from 71 % to 48 % between 1973 and
29
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
2005. Commercial coffee plantation accounted for 30 % of the loss and 70 % of
the loss was due to the local community farming practice.
3.2 Study sites
Two sites were selected in Godere Forest for the present study: a forest around
Bishan Waka Lake in Gubeti Peasant Association and a forest in Dushi Peasant
Association.
Bishan Waka is a small lake surrounded by a forest. Manilkara butugei forms the
20-25 m upper canopy of the forest. The species in the 15-20 m tree layer are
Mimusops kummel, Cordia africana, Celtis africana, Diospyros abyssinica, Morus
mesozygia, Croton macrostachyus, Polyscia fulva, Cassipourea malosana,
Phoenix reclinata, and Olea capensis ssp. welwitschii. Small trees and shrubs
include
Chionanthes
mildbraedii,
Lepidotrichilia
volkensii,
Rothmannia
urcelliformis, Oxyanthus speciosum, Argomuellera macrophylla, Rinorea friisii, and
Dracaena fragrans. Altitude in the forest varies from 1430 to 1560 m. The canopy
is open and enough light reaches the ground. Human pressure on this forest in the
form of logging and conversion to other land use types is relatively minimal.
The forest in Dushi area is a very disturbed secondary forest severely affected by
slash-and-burn agriculture and both semi-forest coffee and commercial coffee
management. The sampling site for the present study is in the semi-forest coffee
managed area at altitude between 1230 and 1270 m. The forest has three layers,
two tree layers and a shrub layer. Trees and shrubs in this area include Antiaris
toxicaria, Millettia ferruginea, Baphia abyssinica, Polyscias fulva, Mimusops
kummel, Strychnos mitis, Diospyros abyssinica, Trichilia dregeana, Croton
macrostachyus, Celtis africana, C. philippensis, Cordia africana, Pouteria
(=Aningeria) altissima, Albizia grandibracteata, Ficus sur, F. mucuso, F. lutea,
Morus mesozygia, Trichilia dregeana, , Trilepisium madagascariense, Malacantha
alnifolia, and Vepris dainellii, The shrubs layer is dominated by Coffea arabica.
Other less abundant shrubs include Argomuellera macrophylla, Maytenus
gracilipes, Alchornea laxiflora, and Dracaena fragrans.
30
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
3.3 Results
3.3.1 Floristic composition
Altogether 75 taxa of foliicolous lichens and lichenicolous fungi growing on
foliicolous lichens belonging to 27 genera and 15 families were recorded from
Godere Forest (Fig. 3.2). Out of these, 70 were identified to a species level, 4
were identified to a genus level and one species was identified to a variety level.
Three species were found to be new to science. The full species list is presented
in Appendix 1.
Species
80
Genus
70
Family
No. of taxa
60
50
40
30
20
10
0
Godere Total
Dushi
Bishan Waka
Fig. 3.2 Distribution of foliicolous lichen taxa in Godere Forest and the study sites
of Bisha Waka and Dushi
About 93 % of the species in Godere Forest were typically foliicolous, 1.3 %
facultatively foliicolous, 1.3 % ubiquitous and 4 % were lichenicolous fungi growing
on foliicolous lichens (Fig. 3.3). Arthonia atropunctata, Opegrapha velata and an
unidentified species of Opegrapha are the lichenicolous fungi recorded from the
forest. Coccocarpia stellata is the facultative foliicolous lichen species and
Fellhanera bouteillei is the ubiquitous lichen.
31
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
Typically foliicolous
Facultative
Ubiquitous
Lichenicolous
Fig. 3.3 Proportion of typical, facultative, and ubiquitous foliicolous lichens and
lichenicolous lichens in Godere Forest
The most dominant lichen family in Godere Forest was Pilocarpaceae with 6
genera and 20 sub generic taxa (Fig. 3.4). Porinaceae was the second largest
family with 2 genera, 13 species and 1 subspecies. The family Strigulaceae was
represented by one genus, 7 species and 2 subspecies. The families
Asterothyriaceae and Gomphillaceae were each represented by 3 genera and 7
species. The families Coenogoniaceae and Ramalinaceae were each represented
by one genus and three species. The families Arthoniaceae, Roccellaceae,
Aspidotheliaceae, and Thelotremataceae were each represented by one genus
and two species. The two taxa of Roccellaceae belonging to the genus Opegrapha
grew para-symbiotically on foliicolous lichens. The families with one genus and
one species were Coccocarpiaceae, Lyromataceae, Monoblastiaceae and
Verrucariaceae.
Among the two sampling sites, higher number of families, genera and species
were recorded from Dushi with 14 families, 24 genera and 68 species. From
Bishan Waka 10 families, 17 genera and 38 species were recorded (Fig. 3.2). The
distribution of foliicolous lichens and lichenicolous fungi in Bishan Waka and Dushi
is presented in Appendix 2.
32
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
Pilocarpaceae
Porinaceae
Strigulaceae
Gomphillaceae
Asterothyriaceae
Ramalinaceae
Coenogoniaceae
Genera
Thelotremataceae
Species
Aspidotheliaceae
Roccellaceae
Arthoniaceae
Verrucariaceae
Monoblatiaceae
Lyrommataceae
Coccocarpiaceae
0
5
10
15
20
25
Number of taxa
Fig. 3.4 Number of species and genera of foliicolous lichens per family in Godere
The following species were recorded from both Dushi and Bishan Waka study
sites: Aspidothelium fugiens, Asterothyrium rotuliforme, Bacidina apiahica, B.
pallidocarnea, Calenia monospora, Calopadia fusca, C. puiggarii, Chroodiscus
verrucosus, Coccocarpia stellata,
Fellhanera bouteillei, F. paradoxa, F.
sublecanorina, Gyalectidium filicinum, Gyalidea epiphylla, Porina cupreola var.
cupreola, P. epiphylla, P. leptosperma, P. nitidula, P. rubescens, P. subpallescens,
P. cf. triseptata, Sporopodium phyllocharis, Strigula nemathora var. hypothelia, S.
nitidula, S. phyllogena, S. smaragdula, Trichothelium africanum,T. pauciseptatum,
and T. epiphyllum.
The species recorded from Dushi but absent in Bishan Waka were Arthonia
atropunctata, A. lividula, Aspidothelium hirsutum sp. nov., Asterothyrium
microsporum, A. octomerum, Bacidina mirabilis, Brasilicia foliicola, Byssolecania
33
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
hymenocarpa, B. chlorinum, B. leucoblepharum, B. subpolychromum, Calenia
triseptata, Calopadia phyllogena, Caprettia goderei sp. nov., Chroodiscus
kakamegensis sp. nov., Coenogonium dilucidum, C. subluteum, C. usambarense,
Fellhanera cf. aurantiaca, F. subfuscatula, F. submicrommata, Lyromma
nectandrae, Opegrapha velata, Porina rubescens, P. rufula, P. tetramera, P.
trichothelioides, Psorotheciopsis varieseptata, Sporopodium antonianum, S.
leprieurii, Strigula schizospora, and Tapellaria bilimbioides
The species rich family in Dushi is Pilocarpaceae with 19 species, followed by
Porinaceae with 15 species and Strigulaceae with 7 species (Fig. 3.5). In Bishan
Waka the family Porinaceae was the richest with 11 species, followed by
Pilocarpaceae with 7 species and Gomphillaceae and Strigulaceae had 5 species
each.
Verrucariaceae
Pilocarpaceae
Porinaceae
Strigulaceae
Gomphillaceae
Asterothyriaceae
Ramalinaceae
Coenogoniaceae
Thelotremataceae
Thelenellaceae
Roccellaceae
Arthoniaceae
Monoblastiaceae
Bishan Waka-Species
Bishan Waka-Genera
Lyrommataceae
Dushi-Species
Dushi-Genera
Coccocarpiaceae
0
5
10
15
20
No. of taxa
Fig. 3.5 Foliicolous lichen genera and species per family in Dushi and Bishan
Waka
34
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
3.3.2 Species frequency
The frequency of occurrences of species in the sample plots of the study sites of
Godere Forest are presented in Fig 3.6. In Dushi most of the species (59%) were
rare. Occasional and very frequent species made 18% and 8% of the whole
species respectively. The frequent species made 7% and the less frequent
species made 6% of the whole species. Only 3% of the species were dominant.
100%
90%
80%
Rare
70%
Occasional
60%
Less frequent
50%
Frequent
40%
Very frequent
30%
Dominant
20%
10%
0%
Bishan Waka
Dushi
Fig. 3.6 Frequency distribution of species in Dushi and Bishan Waka
The dominant species in Dushi were Porina nitidula, P. rubentior, P. epiphylla, P.
cupreola var. cupreola and P. subpallescens. Bacidina apiahica and Porina
leptosperma were the very frequent species. The frequent species were Strigula
phyllogena, Strigula smaragdula, Gyalidea epiphylla, Calopadia fusca, and
Lyromma nectandrae. Calopadia puiggarii, Aspidothelium fugiens, Fellhanera
paradoxa, Trichothelium africanum were the less frequent species. The occasional
species were Brasilicia foliicola, Byssolecania hymenocarpa, Calenia monospora,
Gyalectidium
filicinum,
Strigula
nemathora
var.
hypothelia,
Trichothelium
pauciseptatum. Fellhanera bouteillei, Gyalectidium imperfectum, Strigula nitidula,
Fellhanera subfuscatula, and F. submicrommata. The rare species were Arthonia
atropunctata, A. lividula, Aspidothelium hirsutum sp. nov., Asterothyrium
microsporum, A. octomerum, Asterothyrium rotuliforme, Bacidina mirabilis,
Bacidina
pallidocarnea,
Byssoloma
chlorinum,
B.
leucoblepharum,
B.
subpolychromum, Calenia triseptata, Calopadia phyllogena, Caprettia goderei sp.
35
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
nov., Chroodiscus kakamegensis sp. nov., C. verrucosus, Coccocarpia stellata,
Coenogonium dilucidum, C. subluteum, C. usambarense, Fellhanera cf.
aurantiaca, F. sublecanorina, Opegrapha velata, Porina cf. triseptata, P.
rubescens,
P.
rufula,
P.
tetramera,
P.
trichothelioides,
Psorotheciopsis
varieseptata, Sporopodium antonianum, S. leprieurii, S. phyllocharis, Strigula
macrocarpa,
S.
microspora,
S.
schizospora,
Tapellaria
bilimbioides
and
Trichothelium epiphyllum.
In Bishan Waka 47% of the species were rare and 21% occasional. Unlike Dushi,
the dominant species in Bishan Waka constituted higher proportion (16%). The
less frequent, frequent, and very frequent species constituted 8%, 5% and 3% of
the total species respectively
The dominant species in Bishan Waka were Porina nitidula, P. epiphylla, P.
subpallescens, Calopadia puiggarii, Strigula phyllogena and Gyalectidium
filicinum. Fellhanera paradoxa was the only species designated as very frequent
and Calopadia fusca and Bacidina apiahica constituted the frequent category. The
less frequent species constituted Fellhanera bouteillei, Calenia monospora and
Strigula smaragdula. Asterothyrium leucophthalmum, A. rotuliforme, Coccocarpia
stellata, Gyalectidium fuscum, Gyalidea epiphylla, Porina leptosperma, P.
rubentior and Trichothelium africanum constituted the occasional species. The
rare species were Aspidothelium fugiens, Bacidina pallidocarnea, Chroodiscus
verrucosus,
Echinoplaca
pellicula,
Fellhanera
sublecanorina,
Gyalectidium
imperfectum, Phylloblastia pocsii, Porina cf. triseptata, P. cupreola var. cupreola,
Psorotheciopsis patellarioides, Sporopodium phyllocharis, Strigula nemathora var.
hypothelia,
S.
nemathora
var.
nemathora,
S.
nitidula,
Trichothelium
pauciseptatum, and T. epiphyllum
The frequency occurrences of species in the samples of Godere Forest and in the
study sites of Bishan Waka and Dushi are presented in Appendicies 3, 4 and 5
respectively.
36
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
3.3.3 New records and new species of foliicolous lichens
The foliicolous lichens and lichenicolous fungi recorded in this study are all new
records for Ethiopia. Three species of foliicolous lichens new to science were
recorded from Godere Forest. Furthermore, two more records are expected to be
new to science; however the specimens were not adequate for description. Some
interesting records of foliicolous lichens and lichenicolous fungi are also recorded.
3.3.3.1 Species new to science
1. Caprettia goderei sp. nov. (Monoblastiaceae) (Fig 3.7)
A single collection from Godere Forest producing pale brownish to black, wart
shaped perithecia and tubular pycnidia looking like those of Caprettia
nyssaegenoides was found to be new to science. It has been described and sent
for publication.
A
Fig. 3.7 Caprettia goderei sp. nov. A) Habit
B
B) Conidia in saccus being expelled
from pycnidium
Specimen examined: Godere: Dushi Peasant Association 07016’13 N and
035012’17 E, 1230 m, epiphyllous on Strychnos mitis, 2005, Kumelachew
301(KOBL)
37
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
2. Chroodiscus kakamegensis sp. nov. (Thelotremataceae) (Fig. 3.8)
A single collection from Godere Forest belonging to the genus Chroodiscus which
was lichenicolous on Porina epiphylla and having smooth thallus and 1-3 septate
ascospores was found to be new to science. The smooth thallus points to
Chroodiscus africana described from Ivory Coast (Santesson & Lücking 1999) but
this species had consistently 1-septate ascospores. It was described and sent for
publication.
B
A
Fig. 3.8 Chroodiscus kakamegensis sp. nov. A) Habit,
B) Ascospores (note the
different septation)
Specimen examined: Godere: Godere Forest, Dushi Peasant Association, 1230 m,
07016’13 N and 035012’17 E, epiphyllous on Diospyros abyssinica, Kumelachew
297(KOBL).
3. Aspidothelium hirsutum sp. nov. (Aspidotheliaceae) (Fig. 3.9)
A single collection having small thallus with hairs produced by the fungus and on
which the photobiont growing up from the thallus was collected from Godere
Forest. No member of the genus produced hairs on the thallus and therefore this
collection represents a species new to science. It has been described and sent for
publication.
38
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
A
B
Fig. 3.9 Aspidothelium hirsutum sp. nov. A) Habit, B) Ascospores in ascus
Specimen examined: Godere Forest, Dushi Peasant Association, 1262 m,
07016’56 N and 035012’14 E, epiphyllous on Strychnos mitis, 1262 m Kumelachew
277 (KOBL).
3.3.3.2 Interesting records of foliicolous lichens
1. Calenia sp. (Gomphillaceae) (Fig. 3.10)
Thallus continuous, smooth, pale green, to 2 mm in diameter; apothecia 0.0250.05 mm in diameter, slightly pruinose, ascospores muriform, one per ascus, 3845 x 12-18 µm. This specimen seems to represent a new species, but the material
is scanty for proper description.
Fig. 3.10 Calenia sp.
Specimen examined: Godere Forest, 1230 m, 07016’04 N, 035012’11 E, on living
leaves of Dracaena fragrans, Kumelachew 308, (KOBL)
39
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
2. Fellhanera cf. aurantiaca (Pilocarpaceae) (Fig. 3.11)
Two collections listed below had green thallus; a typical paraplectenchymatous
excipulum with large cells (upto 8-10 µm) under the hypothecium; hypothecium K+
red-brown; ascospores 3-septate, 12-18 x 3-4.5 µm. Our specimens match the
description of Fellhanera aurantiaca from Guinea (Vězda 1974) and also known
from the DR Congo except that the excipullar cells under the hypothecium are not
said to be large. From the photos of Lücking & Colin (2004), our specimen looked
like F. rubida (only known from South America) and said to have very large cells in
the excipulum under the hypothecium (Lücking 1997b).
A
Fig. 3.11 Fellhanera cf. aurantiaca A) Habit
B
B) Excipulum
Specimen examined: Godere Forest, Dushi Peasant Association, 1230 m,
07016’53 N, 035012’11 E, on living leaves of Argomuellera macrophylla,
Kumelachew 3/275 & 1250 m; 07016’16 N, 035012’24 E, on living leaves of
Diospyros abyssinica, Kumelachew 297 (KOBL)
3. Fellhanera aff. bouteillei (Pilocarpaceae) (Fig. 3.12)
The collection cited below had green, rather coherent thallus, apothecia medium
sized, pale orange to brownish orange, with a thin but distinct margin, ascospores
1-septate, 22-25 x 4-5 µm. The collection belongs to the Felhanera subternella
aggregate (Lücking 1997b) and is close to F. bouteillei, a species known to exhibit
variations in thallus and apothecial morphology. It differs from Fellhanera bouteillei
40
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
in thallus morphology and having longer (22-25 µm) ascospores with the proximal
and distant cells being more or less equal in size.
a
b
Fig. 3.12 Fellhanera aff. bouteillei a) Habit b) Ascospore
Specimen examined: Godere Forest, Bishan Waka, 1370 m, on living leaves of
Phoenix reclinata, 2005, Kumelachew 318 (KOBL).
4. Opegrapha sp. (Rocellaceae) (Fig. 3.13)
Ascomata lichenicolous on Strigula phyllogena, asci 8-spored, ascospores 3septate, 10-13 x 2.5-3.5 µm. The size and shape of the asci and size of
ascospores and septation of this collection are similar with those of Opegrapha
phylloporinae. However, the host of our collection is Strigula phyllogena where as
O. phylloporinae grows on Porina conica, P. epiphylla, P. similis, P. virescens
(Matzer 1996).
Specimen examined: Godere Forest, Dushi Peasant Association, 1230 m,
07016’04 N, 035012’11 E, on living leaves of Argomuellera macropylla, 2005,
Kumelachew 304 (KOBL).
41
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
Fig. 3.13 Opegrapha sp., the host is Strigula phyllogena
5. Porina cf. triseptata (Porinaceae) (Fig. 3.14)
Porina triseptata was described by Vězda (1994) as Trichothelium triseptatum but
it was later transferred to the genus Porina by Lücking (1998). The present
collections match perfectly with the description of the species except that
ascospores are shorter (15-25 µm) and lobules, instead of stiff setae, are present
on the perithecia.
Fig. 3.14 Porina cf. triseptata
42
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
Specimen examined: Godere Forest, Dushi Peasant Association, 1232 m,
07016’53 N and 035012’11 E, on leaves of Argomuellera macrophylla,
Kumelachew 1/275 (KOBL).
6. Sporopodium sp. (Pilocarpaceae) (Fig. 3.15)
Two collections had campylidia producing pearl-shaped conidia and thallus is
sorediate. Soredia have so far not been observed in the species of Sporopodium.
Therefore, these collections could represent new taxon of Sporopodium, but
proper description was not possible as the specimens were with out apothecia.
Fig. 3.15 Sorediate specimen of Sporopodium
Specimen examined: Godere Forest, Dushi Peasant Association, 1232 m,
07016’53 N and 035012’11 E, on leaves of Argomuellera macrophylla,
Kumelachew 3/275; 1250 m, 07016’19 N and 035012’21 E, on living leaves of
Argomuellera macrophylla, Kumelachew 290 (KOBL).
7. Trichothelium pauciseptatum (Porinaceae) (Fig. 3.16)
Trichothelium pauciseptatum was described by Vězda (1994) from a collection of
S. Lisowski from the Orientale province (former Haut Zaire) in the DR Congo. The
present collection matches well with the description of the species except for the
color of the tip of the setae. In the description of T. pauciseptatum, setae are black
in color. In our collection, the setae are black with pale tip. In addition, the
43
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
ascospores of Kumelachew 307 were longer (27 x 3 µm), those of Kumelachew
325 were narrower (17.5 x 2.5 µm) and of Kumelachew 293 narrower and shorter
(15-17.5 x 2.5 µm) than the holotype (16-20 x 3-3.5 µm).
Fig. 3.16 Trichothelium pauciseptatum
Specimen examined: Godere Forest, Dushi Peasant Association, 1270 m,
07016’56 N, 035012’14 E, on living leaves of Argomuellera macropylla, 2005,
Kumelachew 284; 1250 m, 07016’19 N, 035012’21 E, on living leaves of Tiliachora
funifera, 2005, Kumelachew 293; 1230 m, 07016’04 N, 035012’11 E, Kumelachew
307; (KOBL).
3.3.2 Alpha-diversity
3.3.2.1 Mean species number
There were more species per sample in Dushi than in Bishan waka. In Dushi a
mean of 11 species were recorded per sample and in Bishan Waka a mean of
8.04 species were recorded (Fig. 3.17). This difference is statistically significant (tvalue 1.98, p<0.05).
44
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
20
18
Mean species number
16
14
12
10
8
6
4
2
0
Dushi
Bishan Waka
Fig. 3.17 Mean number of species per sample per study site of Godere Forest
(values are mean ± SD)
3.3.2.2 Species accumulation curve
Species accumulation (rarefaction) curves were plotted for the foliicolous lichen
species recorded from Dushi and Bishan Waka forest parts of Godere (Fig. 3.18).
The graphs were plotted for the mean number of species against the number of
samples pooled (Fig. 3.18a) and the mean number of species against the number
of individuals pooled (Fig. 3.18b). The first graph compares species density and
the second graph compares species richness.
Although the rate of species accumulation decreased as increasing number of
samples were successively added to the total, neither of the curves reached an
asymptote. The number of species for Dushi was higher than for Bishan Waka at
all levels of sample accumulation. For 24 samples (sample size of Bishan Waka)
pooled, 38 species were observed in Bishan Waka and 59.7 species in Dushi. To
see if there is significant difference in species richness, Magurran (2004)
recommended to check if the observed richness of the smaller community lies
within the 95% confidence limits of the rarefaction curve of the larger community.
Accordingly, the observed species accumulation curve of Bishan Waka is out side
the 95% confidence intervals of the species accumulation curves of Dushi (Fig.
45
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
3.18b) indicating significantly higher species richness in Dushi than in Bishan
Waka.
80
a
No. of species -
70
60
50
40
30
20
10
0
0
10
20
30
40
50
400
500
No. of samples
80
b
No. of species .
70
60
50
40
30
20
10
0
0
100
200
300
No. of individuals
Fig. 3.18 Species accumulation (rarefaction) curves (solid lines) and 95%
confidence intervals (dotted lines) for Dushi (black line) and Bishan Waka (red
line). a) Species density b) Species richness
46
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
3.3.2.3 Estimation of species richness
The Chao 2, first and second order Jackknife, Incidence Based Coverage
Estimator, Bootstrap and the Michaelis-Menten Mean species richness estimators
estimated more species than the observed species (Sobs) for the study sites of
Dushi and Bishan Waka. Table 3.1 presents the observed species number, the
mean (and standard deviation for some) of estimated species. For the study site of
Dushi, Sobs was 68 among 40 pooled samples, and for Bishan Waka 38 species
were observed among 24 pooled samples.
For the data set of Dushi and Bishan Waka study sites, the second order Jackknife
estimated the highest species richness of 82 for Dushi, and 55.2 for Bishan Waka.
On the other hand, MMMeans estimated the lowest species number of 38.6 for
Bishan Waka. Chao 2 estimated the lowest species number of 73.9 for Dushi. The
difference between the highest and the lowest species estimates is 8.1 species for
Dushi, and 11.9 species for Bishan Waka. In all cases, Jack 2 estimator gave the
highest estimates. In Dushi 83-92% and in Bishan Waka 69-88% of the species
richness estimated by the various estimators were collected in this study.
Table 3.1. Number of samples, number of individuals and species richness
estimates values for the study sites of Dushi and Bishan Waka
Dushi
Bishan Waka
No. of samples
40
24
No. of individuals
Sobs
440
68
193
38
MMMeans
Chao 2
Jackknife 1
Jackknife 2
ICE
Bootstrap
Collection degree
76.6
73.9±4.3
81.7±4.5
82
78.2±0.01
75.4
83-92 %
38.6
50±9.2
49.5±4.2
55.2
50.8±0.03
43.3
68.8-87.8 %
3.3.2.4 Shannon-Wiener diversity
47
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
The result of the α-diversity analysis of foliicolous lichens based on ShannonWiener index is presented in Table 3.2. Calculation of t-test showed a very high
significant difference (t-value =3.56, p<0.001) in the Shannon index of Dushi and
Bishan Waka evidencing a higher α-diversity in Dushi than in Bishan Waka.
Table 3.2 Values of Shannon-Wiener and Simpson diversity indices
Dushi
Bishan Waka
Shannon index (H’)
3.72
3.17
Shannon evenness index (J’)
0.88
0.87
3.3.3 Beta-diversity and similarity in species composition
Total β-diversity, measured as total species number divided by mean number of
species in samples, for Dushi and Bishan Waka is presented in Table 3.3. Total βdiversity is higher (6.2) for Dushi than for Bishan Waka (4.7). The similarity in
species composition between Dushi and Bishan Waka computed from Sørensen
index of similarity is not found to be high (Ss=0.58).
Table 3.3 β-diversity along the study sites of Dushi and Bishan Waka
Number of
species (a)
Mean number of
species per sample (b)
β-diversity
(a/b)
Dushi
68
11
6.2
Bishan Waka
38
8.04
4.7
Sørensen index of similarity (Ss) between Dushi and Bishan Waka
Number of shared
species
Ss
31
0.58
48
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
3.3.4 Ordination
The Detrended Correspondence Analysis (DCA) of the presence/absence data of
Godere ordered the samples and species along the ordination axes. The first DCA
axis with eigenvalue of 0.395 explained 11.9% of the variation and the second axis
with eigenvalue of 0.192 explained 5.8% of the variation. Thus most of the
variation in site condition and species composition can be explained by the
gradient corresponding to the first DCA axis. Eigenvalues of the third and fourth
axes are 0.158 and 0.116 respectively.
In the sample ordination plot (Fig. 3.19), samples from less disturbed sites are
distributed along the left side of the first DCA axis, and samples from high
disturbed sites are distributed along the right side. The variation in the distribution
of samples along the first axis of DCA is thus explained by difference in
disturbance level. Most of the samples from Bishan Waka are distributed along the
gradient where disturbance is higher and the samples from Dushi are distributed
along the gradient where disturbance is lower.
Fig. 3.19 DCA diagram of samples of Godere Forest. Green circles = samples
from Dushi, black squares = samples from Bisahn Waka.
49
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
The species ordination diagram (Fig. 3.20) shows that species from highly
disturbed samples are distributed on the right side of the first DCA axis and
species from less disturbed samples are distributed on the left side of the first axis.
The first group of species includes Asterothyrium rotuliforme, A. octomerum,
Gyalectidium filicinum, Calenia monospora, Calopadia puiggarii, Gyalectidium
fuscum, and Fellhanera bouteillei. Among the second group of species include
Porina leptosperma, P. rubescens, P. cupreola var. cupreola, Byssolecania
hymenocarpa, Arthonia lividula, and Coenogonium dilucidum.
Fig. 3.20 DCA diagram of species of Godere Forest. Green squares = shady
understorey species, red circle = light gap and canopy, black circle = species with
wide amplitude. For clarity only some of the species are shown. For Acronyms see
Appendix 1.
50
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
3.3.5 Phorophytes
Various phorophyte species were hosts of foliicolous lichens in Godere Forest
including Argomuellera macrophylla, Baphia abyssinica, Blighia unijugata, Coffea
arabica, Dracaena fragrans, Hippocratea africana, Landolphia buchananii,
Manilikara butugi, Olea capensis ssp. welwitschii (=O. welwitschii), Phoenix
reclinata, Piper guineense, Rinorea friisii, Strychnos mitis, Tiliachoa troupinii, and
Trilepisium madagascraiense. Of these, Argomuellera macrophylla is the
phorophyte that supported the highest species of foliicolous lichens (58 species).
Strychnos mitis supported 28 species, Dracaena fragrans supported 25 species,
Diospyros abyssinica supported 24 species, and Trilepisium madagascariense
supported 22 species. Coffea arabica, the most abundant shrub in Dushi,
supported only 10 species of foliicolous lichens.
3.4 Discussion
3.4.1 Foliicolous lichen flora
All the foliicolous lichens recorded in this study are the first record for Ethiopia.
The checklist of lichens and lichenicolous fungi (Feuerer 2007), listed 279 species
of lichens from Ethiopia. However, foliicolous lichens were not included in the
checklist indicating that no foliicolous lichens were collected until this time.
Ethiopia is a tropical country with varied climatic and topographic features resulting
in diverse flora and vegetation types which could also support high lichen diversity.
However, cryptogams in general and lichens in particular have been overlooked
for so long that the lichen flora of the country is almost unknown. The book on
macrolichens of East Africa (Swinscow and Krog 1988) incorporates some lichen
species collected by Hildur Krog from the southern part of Ethiopia in 1971. This
book is the first and the only available source of information for the lichens of
Ethiopia.
Tropical rainforests are the suitable habitats for foliicolous lichens (Santesson
1952, Lücking 1995). In Ethiopia most of the natural forests are Afromontane type,
distributed at altitudes above 1500 m. Forests of a lowland type are very restricted
in parts of southwestern Ethiopia. Floristically, Godere Forest occupies a
51
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
transitional position between a lowland Guineo-Congolean rainforest and
afromontane rainforest of the higher altitude. However considering the topographic
position and climatic features of the forest with high temperature and rainfall, it is
the most suitable habitat for foliicolous lichens. However, due to shifting cultivation
and the semi-forest coffee management system, no trace of undisturbed natural
forest can be found in Godere. The foliicolous lichens recorded in this study came
from a disturbed secondary forest and it is not known what the foliicolous lichen
flora of an undisturbed primary forest would have looked like. A number of species
(e.g Coenogonium geralense, C. pocsii) which would be expected in a primary or
old growth forest were not recorded from the forest.
The tropical forests of Africa are the least explored in terms of their foliicolous
lichens. This is reflected by the number of new species or species of interesting
characters recorded from Godere. Considering the continuous anthropogenic
disturbance affecting the forests, it is highly probable that several species of
foliicolous lichens have locally been extinct.
Most of the samples in this study were from the study site of Dushi since it covers
the most part of Godere Forest. The forest surrounding Bishan Waka Lake was
selected for this study since it was not utilized for coffee development and largescale logging did not take place. However, the forest is a fragment isolated from
the large mass of forest in Godere and forms an island surrounded by human
settlement and cultivation. In addition it covers a very small area around the lake
and the distance between the forest edge and the interior is very small.
Consequently, the available habitat for the growth of foliicolous lichens is
considerably lower than in Dushi. Due to its isolation from the large main forest
block, there are no enough sources of diaspore for the establishment of foliicolous
lichens. These might be the reasons for the low foliicolous lichen diversity
compared to the study site of Dushi.
In a natural forest, three major light regimes or microsites (the shady understorey,
the natural light gap and the canopy) and two transition types (transition to light
gap and transition to outer canopy) are distinguished (Lücking 1997). In Dushi, the
shady understorey light regime is reduced due to removal of some canopy trees
which the farmers assumed to have impact on the growth and quality of the coffee
52
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
plant. In addition many possible phorophyte individuals were removed to enhance
the growth of coffee beans. Therefore, the available microsite conditions and
phorophyte individuals are fewer compared to undisturbed forest. However, the
proportion of shady understorey species is higher in Dushi (52.4%) than in Bishan
Waka (39.5%) and the proportion of light gap and canopy species are higher in
Bishan Waka (50% light gap, 10.5% canopy) than in Dushi (42.6% light gap, 4.9%
canopy).
3.4.2 Alpha-diversity
Ecologists often need to know the number of species (species richness) found in a
given area or they need to compare the number of species in different areas
(Colwell et al (2004). Complete enumeration of all species of a given area is often
difficult for many groups of organisms including lichens. Various methods are now
available for the estimation of species richness from available samples. These
methods have mostly been applied for the estimation of the richness of animals
(Toti et al. 2000, Longino et al. 2002, Schulz and Wagner, Sørenson 2004), plants
(Butler & Chazdon 1998, Chazdon et al.1998, Chiarucci et al. 2003) and lichens
(Nöske 2004). Using non-parametric species richness estimators the species
richness of foliicolous lichens has been for the first time estimated in this study.
The sample sizes of Dushi and Bishan Waka are very different and comparison of
species richness based on different sample size is misleading. Using the species
accumulation curve (rarefaction curve), however, species richness can be
compared at comparable sample size. The lowest sample size of the areas to be
compared is usually selected as a basis for comparison. As it can be seem from
the rarefaction curves and their 95% confidence intervals, there are significantly
more foliicolous lichen species in Dushi than in Bishan Waka. The high diversity of
foliicolous lichens in Dushi as compared to Bishan Waka is due to the availability
of different microsite habitats in the former than in the latter.
The degree of foliicolous lichen collection or sample sufficiency can be evaluated
based on the degree to which species accumulation curves approach a horizontal
asymptote, the rate of accumulation of new species or using the predicted values
of the species richness estimators. (Soberón and Llorente 1991, Gotelli and
53
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
Colwell 2001). If the species accumulation curve reaches a stable asymptote, it is
an indication of adequate sampling. As additional samples are pooled and the
observed species richness curve stabilizes beyond a particular number of
samples, then the observed species richness is considered as adequate estimate
of community species richness for that number of samples (Longino et al. 2002).
Although the species accumulation curves of Dushi and Bishan Waka did not
reach an asymptote, the rates of accumulation of new species as more samples
were pooled have decreased. From Dushi 83% of the species were collected
based on the highest estimator and 92% of the species were collected based on
the lowest estimator. From Bishan Waka 69% of the species were collected based
on the highest estimator and 88% of the species were collected based on the
lowest estimator. Heck et al. (1975) reported that collection of 50-75% of the total
number of species of a given area might be satisfactory. Accordingly, the sampling
efficiency for Dushi and Bishan Waka can be considered satisfactory.
The 95% confidence intervals of the species accumulation curves of Dushi and
Bishan Waka (Fig. 3.18) did not overlap indicating the presence of significant
difference in species richness. Colwell et al. (2004), comparing tropical rain forest
sampling in old growth and second growth forests, concluded that when
confidence intervals overlap, the differences in species richness is not significant
and when confidence intervals do not overlap the differences in species richness
is significant.
In Bishan Waka, the species richness estimators predicted that more species are
yet to be sampled than from Dushi. This is due to the higher number (31.6 %) of
uniques (species restricted to one sample only) in Bishan Waka. In Dushi uniques
accounted for 20.6 % of the whole species. Species richness estimators use the
frequency of rare species to predict the total sample species richness (Williams et
al. 2007). The presence of many rare species means higher probability of
encountering more new species with increased sampling effort.
Considering the results of the species accumulation curve and Shannon diversity
index, it can be concluded that α-diversity is significantly higher in Dushi than in
Bishan Waka.
54
Diversity of Foliicolous Lichens in Godere Forest, Ethiopia
3.4.3 β-diversity
The proportion of shared species of Dushi with the total foliicolous lichen flora of
Godere is 91% and that of Bishan Waka 51%. Total β-diversity, calculated by
dividing the total species number by a mean number of species in a sample,
indicates the degree of turnover (species change). The higher total β-diversity of
Dushi is an evidence for a higher species turnover than in Bishan Waka. The
similarity in foliicolous lichens composition between Dushi and Bishan Waka, as
measured by the Sørenson index, is medium (Ss=0.58) showing a medium species
turnover.
3.5 Conclusion
The present study has shown that:
•
both alpha and beta diversity are higher in Dushi than in Bishan Waka.
•
low diversity in Bishan Waka is because of it is fragmented nature and
isolation from the main forest by cultivations and settlement.
•
the effect of human disturbance on foliicolous lichens diversity in Dushi is
mainly due to the removal of phorpohytes from the shrub stratum.
•
the variation in foliicolous lichens diversity between Dushi and Bishan
Waka can be explained by the difference in the level of disturbance. This
has been shown in the ordination diagram where samples distributed along
the low disturbance gradient were from Dushi and samples from the high
disturbance gradient were from Bishan Waka.
•
the forest canopy is relatively closed in Dushi and thus there are more
shady understorey species and low light gap species in Dushi than in
Bishan Waka.
•
semi-forest coffee management system maintains foliicolous lichen
diversity than land uses such as cultivation and clear-cutting that may
result in partial or complete removal of forest vegetation.
55
Diversity of Foliicolous Lichens in Budong Forest, Uganda
Chapter 4 DIVERSITY OF FOLIICOLOUS LICHENS IN
BUDONGO FOREST, UGANDA
4.1 Study area
4.1.1. Location and physiography
Budongo Forest Reserve lies in western Uganda, in Masindi District, Bujenje,
Buliisa and Buruli Counties (Muhereza 2003). It is situated on the top of the
escarpment east of Lake Albert on the edge of the western rift valley (Howard et
al. 1996; Sheil 1999, 2001, Sheil et al. 2000) between 1037’ and 2003’ N latitude
and 31022 and 31046’E longitude (Sheil 1999, 2000, 2001; Reynolds 2005) (Fig.
4.1). The Budongo Forest Reserve is divided into two parts by the road connecting
Masindi and Butiaba which is located on the shore of Lake Albert; the northeastern
part is called the Budongo and the other is called the Siba (Sugiyama 1968). The
reserve lies approximately 10 km west and north of Masindi and 10 km east of
Lake Albert (Howard et al. 1996).
Fig. 4.1 Map of Uganda and the location of Budongo Forest (red square). Source:
CIA World Factbook
56
Diversity of Foliicolous Lichens in Budong Forest, Uganda
Fig. 4.2 Satellite imagery of Budongo Forest showing sampling sites (red squares).
(Source: BIOTA E02).
The gazetted area of Budongo Forest Reserve includes four forest blocks viz.
Siba, Budongo, Kaniyo-Pabidi and Kitigo (Fig. 4.2). The reserve covers an area of
almost 793 km2, of which 428 km2 is closed forest; the rest is savanna woodland
or grassland (Howard et al. 1996; Sheil 1997, Sheil et al. 2000, Plumptre 2001).
The reserve lies at altitudes between 950 and 1200 m, with mean altitude of 1100
m (Plumptre 2001), on gently undulating terrain with a gentle NNW slope to the
edge of the rift escarpment. There are few steep ridges and no deep gullies
(Eggeling 1940). Several isolated hills of similar heights rise above the general
level of the forest, the most prominent of which are Kasene (1171 m a.s.l.), Kaniyo
(1187m a.s.l.), Lukoho (1160 m a.s.l.), Nyabyeya (1247 m a.s.l.), Little Kasenene
57
Diversity of Foliicolous Lichens in Budong Forest, Uganda
(1173 m a.s.l.), and Busingiro (1201 m a.s.l.) (Howard 1991). The valley bottoms
mostly contained ‘swamp forest’, but the ground there, though soft, is rarely
swampy.
Budongo Forest is a catchment area for four small rivers which flow north-west
through the forest, over the escarpment and into Lake Albert. (Eggeling 1947;
Paterson 1991, Reynolds 2005). These rivers from east to west are the Waisoke,
the Sonso, the Kamirambwa and the Siba (Reynolds 2005).
4.1.2. Geology and Soil
Crystalline rocks of the Ancient Basement Complex of Pre-Camberian origin,
intruded by granites, underlie Budongo Forest. The Basement Complex is an
assemblage of schistose and gneissose rocks which are metamorphosed
sandstones, shales, limestones, and eruptives. (Eggeling 1947). It is from these
rocks that the soils are formed.
Advanced laterization in the Budongo area is likely to have coincided with
peneplanation and the hills around and in the forest indicate the past level of the
lateritic blanket which once covered the whole area. Following the Rift uplift, which
resulted into the formation of the Western Rift Valley, it is probable that
widespread erosion removed the greater part of the laterite and led to the
formation of fresh soils from crystalline rocks, some of which were quickly
colonized by forests (Philip 1996, Sheil 1996).
The soils of Budongo are predominantely tropical red earths (Eggeling 1947,
Paterson 1991), of a type regarded as almost the final stage in tropical weathering.
These soils are red in profile and vary from a heavy loam or sandy clay to a very
sandy loam characteristic of the many of the valley bottoms (Eggeling 1947).
These soils are termed as ‘ferralitic’ (Sheil 2001). A second much less common
soil type called ‘murram’ is localized in the forest on low rounded ridges or gentle
slopes and is always underlain by quartzose rocks. (Eggeling 1947). This soil has
undergone laterization and varies from a red loam containing small concentrations
of ironstone, capable of supporting forest, to tiny ridge-top pavements of solid
cellular ironstone (Eggeling 1947).
58
Diversity of Foliicolous Lichens in Budong Forest, Uganda
4.1.3. Climate
Unlike many forest areas in Africa, there is a long-term climatic data for Budongo
Forest. In 1937 five meteorological stations were established in Budongo Forest.
Of these, four stations were established inside the forest and one outside the
forest (Eggeling, 1947). The data are summerized by Eggeling (1947), Paterson
(1991) and Sheil (1997).The Budongo Forest Project has been collecting rainfall
and temperature data since 1993 (Reynolds 2005).
Rainfall in Budongo is bimodal with two peaks from March to May and from
September to November with monthly rainfall more than 150 mm (see Fig.4.3).
There is only one dry season from mid December to mid February with monthly
rainfall not more than 50 mm. Annual rainfall is between 1200-1800 mm (Sheil
1995, 1997, 1998; Reynolds 2005). The annual minimum mean temperatures in
Budongo Forest range from 17 to 200C and maximum mean temperatures range
from 28 to 290C (Howard 1991).
Rain fall (mm/mont
250
200
150
100
50
Dec
Nov
Oct
Sept
Aug
Jul
Jun
May
Apr
Mar
Feb
Jan
0
Month
Fig.4.3 Mean monthly rainfall (mm) records from 1944 to 1989 in Nyabyeya
meteorological station. Source: Sheil (1997)
4.1.4. Biotic attributes
4.1.4. 1 Vegetation and flora
Budongo Forest is among the easternmost outlier blocks of the Congo basin forest
(Paterson 1991). Based on its structure and constituents, Eggeling (1947)
described Budongo as lowland rain forest. Langdale-Brown et al. (1964) classified
59
Diversity of Foliicolous Lichens in Budong Forest, Uganda
Budongo as a medium altitude moist semi-deciduous forest. Hamilton (1974)
classified the lowland forests of Uganda into four zones, viz. the Parinari, the
Celtis-Chrysophyllum, the Cynometra-Celtis, and the Piptadeniastrum zones. The
Celtis-Chrysophyllum and the Cynometra-Celtis zones are represented in
Budongo Forest. Philip (1965) and Howard (1991) classified Budongo as moist
semi-deciduous tropical forest. According to Paterson (1991), the vegetation of
Budongo Reserve consists of a rich mixture of rainforest communities and a broad
intermixture or ecotone with the surrounding tree savannas and grasslands.
Eggeling (1947), Synnott (1985), Paterson (1991), and Sheil et al. (2000)
described the flora of Budongo Forest. Of these, Synnott (1985) provided the full
plant species composition including 240 species of trees, 123 species of shrubs,
19 species of scrambling shrubs, 66 species of woody climbers and lianas, 61
species of herbaceous climbers, 246 species of terrestrial herbs, 109 species of
vascular epiphytes, 1 parasitic species and 1 saprophytic species. Howard et al.
(1997) reported 465 species of trees and shrubs for Budongo Forest. Budongo
Forest has the largest number of tree species recorded in the Ugandan forest
(Howard 1991, Sheil 1996) and it is the richest mahogany forest in Uganda (Lind
and
Morrison
1974,
Howard
et
al.
1997).
Artabotrys
lastoursvillensis,
Discoglypremna caloneura, Iodes africana, Mammea africana, Microdesmis
puberula, Ritchiea aprevaliana and Telfairia occidentalis are species limited to
Budongo Forest in Uganda (Synnott 1985).
Based on the observations of earlier workers (Haris 1934, Brasnett 1946),
Eggeling (1947) described the natural forest types of Budongo Forest and
proposed succession from colonizing forest through mixed forest to climax forest.
This successional model was later conformed by Sheil (1999) with objective
measures of development.
According to Eggeling (1947), the Budongo Forest contains four forest types viz.
colonizing forest, mixed forest, Cynometra forest, and swamp forest.
1. Colonizing forests are of two types: the Maesopsis and woodland forest. The
Maesopsis colonizing forest is found in slightly better soil than the woodland forest.
It is composed of a matrix of colonising species such as Maesopsis eminii, Cordia
60
Diversity of Foliicolous Lichens in Budong Forest, Uganda
millenii and Diospyros abyssinica. Maesopsis eminii forms 50-80 percent of the
canopy. The woodland forest is found on poorer or shallow soils, and is composed
of Olea welwitschii, Phyllanthus discoideus and Sapium ellipticum in the upper
story with a general domination of the understorey by Calconcoba and old remnant
Terminaila derived from the tree savanna (Eggeling 1947; Paterson 1991).
2. Mixed forest is the richest of the forest type in number of tree species, covers
much of the forest and contains the valuable mahoganies (Eggeling 1947,
Paterson 1991, Plumptre 1994). The most common species are Celtis mildbraedii,
C. zenkeri, Chrysophyllum albidum, C. perpulchrum, Funtumia elastica and the
mahoganies Khaya anthotheca, Entandrophragma cylindericum, E. angolense,
and E. utile.
3. Cynometra (Ironwood) forest is the climatic climax forest of Budongo (Eggeling
1947). It is characterized by the abundance of Cynometra alexanderi, which
accounts for up to 35 percent of all trees and as much as 90 percent of all large
trees. Other typical tree components include Strychnos mitis, Celtis wightii, and C.
mildbradeii. The understorey is characterized by Lasiodiscus mildbraedii.
4. Swamp forest is found in valley bottoms in which the soil is flooded by
permanent and seasonal slow running streams. The dominant tree is Mitragyna
stipulosa. Others include Pseudspondias microcarpa, Parkia filicoidea, Erythrina
excelsa, Bombax bunopozense subsp. reflexum, Macaranga schweinfurthii and
Bridelia micrantha.
According to Eggeling (1947) the first three forest types follow an ecological
succession from the colonizing forest to mixed forest and finally to Cynometra
forest with colonising-mixed and Cynometra-mixed transitions. The Cynometra
forest is an ecological climax and the swamp forest is an edaphic climax.
4.1.4.2 Fauna
Budongo Forest is known for its diversity of fauna with 24 species of small
mammals including nine primates, 289 species of butterflies and 130 species of
large moths (Howard et al. 1997). There are 366 species of birds out of which 197
61
Diversity of Foliicolous Lichens in Budong Forest, Uganda
species are forest dwellers (Friedmann & Williams 1973, Owiunji & Plumptre
1998).
Some of the mammals in the forest are tree hyrax (Dendrohyrax buck), red duikers
(Cephalophus rufilatus), blue duikers (C. monticoloa), bush buck (Tragelaphus
scriptus), bush pig (Potamochoerus porcus), porchpines (Hystrix cristata) and
guines fowls (Guttera edouardi). Four species of monkeys live in Budongo Forest
(Reynolds 2005) viz. baboon (Papio anubis), black and white colobus monkey
(Colobus guereza), redtail monkey (Cercopithecus ascanius), and blue monkey
(C. mitis). Potto (Periodicticus potto) is the commonest species of prosimian in
Budongo Forest. Budongo is also home to one of the largest populations of
chimpanzees (Pantroglodytes schweinfurthii) in Uganda with a population of about
700 (Tweheyo et al. 2004).
4.1.5. Management History
The management history of the Budongo Forest Reserve is well documented
(Eggeling 1947, Paterson 1991, Plumptre, 1994, 1996; Reynolds 2005). The value
of Budongo Forest had been recognized as early as 1905 when a permit was
granted to a European firm for the tapping of wild rubber (Funtumia) (Eggeling
1946). In 1932 the British colonial administration gazetted the Budongo Forest an
Undemarcated Forest reserved to the Crown (Eggeling 1947).
4.1.5.1 Forest administration
Since 1920 Budongo Forest was administered by the Forest Department of the
colonial administration. After independence, it was administered by the Forest
Department of the central government. Since 1993 forest management in Uganda
has been decentralized to district and sub-county councils and Budongo Forest
was administered by the Masindy District Council as Central Forest Reserve.
Since 1998 the administration of central forest reserves was transferred to the
central government and the management of Budongo Forest rested under the
Forest Department which was later replaced by a semi-autonomous National
Forestry Authority (Muhereza 2003).
62
Diversity of Foliicolous Lichens in Budong Forest, Uganda
4.1.5.2 Management plan
Management plans were prepared for Budongo Forest for the periods 1935-1945,
1945-1955, 1955-1965, and 1997-2007. The plans indicate the principles of
management of the forest including ways of demarcation, licensing for timber
cutting and silvicultural methods. For the sake of management, Budong forest was
divided into 68 compartments in the Siba, Bullaba, Biiso, Nyakafunjo, Waibira, and
Kaniyo-Pabidi forest blocks.
The current management plan (Kamugisha and Nsita 1997) which covers the
period from July 1997 to June 2007 provides emphasis for biological conservation.
The plan separates the forest into zones for conservation, commercial use,
community use, recreation and research. The majority of Budongo Forest is
earmarked as a production zone for the utilization of timber. The plan establishes
‘Conservation Working Circle’ which includes Strict Nature Reserve (SNR) and
Buffer Zones. The SNR is maintained for biodiversity conservation and water
catchment and tree felling is strictly prohibited. New compartments, mostly in the
Waibira block, are included in the SNR raising the number of compartments to 17.
The buffer zone which includes 14 compartments is established around the nature
reserve to separate the SNR from the production zone. The total area allocated for
the nature reserve is 11,722 ha and 5,293 ha for the buffer zones.
4.1.6. Human Impact
4.1.6.1 Fire
In the 19th century, anthropogenic fire used to control the spread of Budongo
Forest into the surrounding savanna (Paterson 1991). Annually the local people
who live around Budongo Forest set fire to clear away dry growth from the
previous year and produce fresh grass for their cattle. The fire which started this
way also cleared away the savanna and expanded to the edges of the forest.
These fires kept the forest blocks of Budongo and Siba from spreading into the
surrounding savanna land. This process continued until the arrival of Europeans
who controlled fires and managed the forest for timber (Paterson 1991).
63
Diversity of Foliicolous Lichens in Budong Forest, Uganda
4.1.6.2 Logging
Logging in Budongo Forest started in a regular basis in 1917 (Paterson 1991). By
then only small amounts of timber were cut on the southern side of the Budongo
Forest block using pitsaws (Eggeling, 1947). Timber cutting became mechanized
when the first sawmill was established towards the end of 1926 (Eggeling 1946).
From this time onwards, there has been considerable exploitation by concession
holders operating in two concessions, one in the Siba and another in the Budongo
Forest block.
Of the 68 forest compartments, logging took place on the 60 compartments. One
compartment in Nyakafunjo block (N15), 4 compartments in the Waibira block
(W17, W30, W31, W32), and 3 compartments in the Kaniyo-Pabidi block (K11,
K12, K13) were left unlogged. The compartments N15, W17, W30, W31, and W32
are protected as nature reserve (Plumptre 1996, Owiunji & Plumptre 1998).
The
main
timbers
exploited
were
Khaya
anthotheca,
Entandrophragma
cylindericum, E. angolense, E. utile, Cynometra alexanderi, Erythrophleum
guineense, Mildbraediodendron excelsum., Maesopsis eminii, Alstonia congensis,
Ricinodendron africanum, Chlorophora excelsa, and Morus lactea. Table 4.1
shows the volume of mahoganies and other timbers extracted from the various
forest blocks of Budongo between 1928 and 1992. In the Biiso, Nyakafunjo,
Waibira and Kaniyo forest blocks, more than 60 percent of the timbers extracted
were mahoganies. In the Siba block 42 percent of the timbers extracted were
mahoganies. In general, 872,627 m3 of timber were extracted in the 60 years
period (Plumptre 1996).
Paterson (1991) and Plumptre (1996) summarized the logging activities in
Budongo Forest between 1930 and 1970. At the beginning, logging operations
was aimed at extracting all the old timber trees above 1.3 m diameter at breast
height (DBH) and creating a two-stage uniform crop of trees which would be felled
at 40-year intervals (polycyclic felling). In the 1950s research showed that damage
to the forest due to the logging operations and the slow growth rates of the trees
meant that polycyclic felling would lead to lower yields than felling on longer
cycles. Therefore the logging plans were changed to monocyclic felling at 80-year
64
Diversity of Foliicolous Lichens in Budong Forest, Uganda
intervals and felling limits of timber trees were reduced to 85 cm DBH. Replanting
of mahoganies was carried out in logged areas during the 1940s and early 1950s.
However, research showed that natural regeneration was successful and
replanting ceased by the mid 1950s.
Table 4.1 Volume of timber extracted in the Budongo Forest blocks between 1928
and 1992. (Source: Plumptre 1996).
Forest
block
Area
(ha)
Biiso
4350
Nyakafunjo
8134
Waibira
21358
Kaniyo
4818
Siba
5288
Year logged
1935-1944,
1981-1992
1945-1954,
1956-1962
1960-1976,
1978-1980
1970-1972,
1977, 19851992
1928-1935,
1963-1977,
1979, 1990
Volume of
timber
extracted
(m3ha-1)
219.7
Volume of mahogany
extracted
(m3ha-1)
535.7
371.7
448.9
282.7
103.7
65.6
118.1
49.8
152.9
In addition to mechanized harvesting of timber, harvesting by pitsawing used to
take place in some compartments in the 1980s (Plumptre 1996). After realizing
that mechanized logging was harmful to natural regeneration, the Uganda Forest
Department in the 1990s started providing license to organized pitsawyers to carry
out selective extraction of mahoganies and other timber trees (Muhereza 2003).
Between 1991 and 1996 the annual off-take of timber by pitsawyers and saw
millers averaged 11,522.82 m3 of round wood (Muhereza 2003). At present
mechanized logging is not taking place as all the sawmills are not opereting.
However, illegal pitsawing has been taking place in various parts of the forest
including the SNR (Muhereza 2003; Reynolds 2005).
4.1.6.3 Silviculture
In the 1950s and 1960s, silvicultural measures were taken in order to promote the
growth and regeneration of the most valuable timber species, such as Khaya and
65
Diversity of Foliicolous Lichens in Budong Forest, Uganda
Entandrophragna spp (Plumptre 1996). It was found that opening up the canopy
during the logging operation aided the growth of the mahoganies. Consequently,
arboricide, made from 1:2 mixture of butyl esters 2,4,5-T and 2,4-D dissolved in
diesel oil, was applied to trees that were not marketable, particularly Cynometra. A
total of 34 blocks were treated with arboricide. In 1970 the treatment ceased when
more trees became marketable and it became difficult to import the chemicals.
4.1.6.4 Wild animal control
Budongo Forest used to harbour a good population of elephants, buffalo, wild pigs
and leopards. Control shooting and legal and illegal hunting have diminished the
population of these animals to an alarming level. Rinderpest epidemic in 1889 in
the Bunyoro area eliminated most of the cattle. (Paterson 1991). Epidemic of
trypanosomiasis at the beginning of the 20th century initiated the colonial
administration killing of most of the large wild mammals including buffaloes, wild
pigs, bushbuck and Uganda kob (Harris 1934). The decline of these animals
resulted in substantial increase of the elephant population in the areas of Budongo
Forest to the extent that they converted most of the woody vegetation to treeless
grasslands (Paterson 1991). Elephant control measures started in 1928 (Paterson
1991) under the Uganda Game Department in order to protect the young
individuals of valuable timber species.
4.1.6.5 Population pressure
The population of Masindi District is growing at a high rate. It increased from
260,796 in 1991 to 466,204 in 2002 (Muhereza 2003). The populations of
Budongo and Bwijanga sub-counties near Budongo Forest increased from 44,054
to 76,929 during the same period (Muhereza 2003). This population increase is
leading to encroachment to the forest, increased fuelwood collection and, charcoal
production and illegal pitsawing.
66
Diversity of Foliicolous Lichens in Budong Forest, Uganda
4.1.7 Effects of previous management measures
4.1.7.1 Effects on vegetation
The management history of Budongo Forest has resulted changes in the
distribution of forest types and structure. Areas of colonizing-mixed forest in the
Biiso area developed into mixed forest and areas of mixed forest in compartment
N15 developed into Cynometra-mixed forest. The ironwood forest which covered
32 % of the main Budongo Forest block in 1944 (Eggeling 1947) reduced to 15 to
20 % by 1970 (Paterson 1991). Comparison of the forest type maps of 1951 and
1990 (Plumptre 1996) shows that there was a marked increase in the spread of
the mixed forest at the expense of Cynometra forest. The mixed forest increased
by 41% while the Cynometra forest decreased by 24% (Plumptre 2001).
Logging and silvicultural treatment have also resulted change in the structure of
the forest. Basal area, bole and crown heights, and crown position decreased in
the logged than the unlogged compartments, while lianas were more abundant in
the logged than unlogged compartments (Plumptre 1996). Logging and arboricide
treatment, however, did not result changes in the tree species composition of the
forest. Plumptre (1996) showed that geographical position of the forest
compartment with in the forest influenced the forest composition before and after
logging and arboricide treatment.
4.1.7.2 Effects on fauna
Plumptre (2001) studied the densities of primates, rodents, birds, and frogs in
unlogged and selectively logged compartments in Budongo Forest. The result
showed that the densities of blue monkey, redtail monkey and black and white
colobus monkey increased in the logged compartments while the densities of olive
baboon and chimpanzee showed no difference. The density of rodents was
significantly higher in the unlogged than the logged compartment. The result on
birds showed that most species did not show significant differences between
logged and unlogged forest. Frugivore, bark-gleaning insectivore, nectarivore and
omnivore birds constituted higher percentage in the logged than unlogged forest
compartments. Leaf-gleaning and Sallying insectivore birds constituted higher
percentage in the unlogged than the logged compartments. Diversity of frogs was
67
Diversity of Foliicolous Lichens in Budong Forest, Uganda
higher in the logged than the unlogged compartments. Study of canopy ants and
beetles in logged and unlogged compartments in Budongo Forest (Wagner 2000,
Schultz and Wagner 2002) showed that canopy ant and beetle species are more
diverse in the unlogged than logged compartments while abundance of
phytophagus beetles is higher in the logged than unlogged compartments.
4.2 Study sites
In Budongo Forest, foliicolous lichen sampling took place in Cynometra alexanderi
primary forest (hereafter called primary forest), primary swamp forest (hereafter
called swamp forest), old secondary forest and young secondary forest (Fig. 4.4).
Fig. 22 Fig. 4.4 Study sites of Budongo forest
In the primary forest, the upper 30-40 m canopy is dominated by Cynometra
alexanderii, Khaya anthotheca and Entandrophragma utile. C. alexanderi accounts
for 35% of all trees and as much as 90% of all large trees (Paterson 1991).
68
Diversity of Foliicolous Lichens in Budong Forest, Uganda
Lasiodiscus mildbraedii is a common understorey tree. Due to the closed canopy,
no light reaches the forest interior. As a result, the shrub layer and the ground floor
are sparse. The primary forest has never been logged and it is protected as nature
reserve. From this site, 41 phorophyte individuals were sampled.
The swamp forest is a type of primary forest which is flooded in the wet season
and waterlogged during the dry season (Eggeling 1947, Paterson 1991). It is the
smallest asscociation in Budongo (Paterson 1991). It is two storied, with irregular
canopy. Lianas and straggling figs are abundant. Logging did not take place in this
forest type. From this site, 64 phorophyte individuals were sampled.
The old secondary forest has four tree layers, with abundance of large trees 25 to
55 meters high (Paterson 1991). The canopy is formed by evergreen trees and
Cynometra alexanderi which is leafless for short time. Other common trees are
Chrysophyllum albidum, Khaya anthotheca and Trichilia.emetica. In this site, trees
were logged between 1947 and 1952. Twenty-two phorophytes individuals were
sampled from this site.
The young secondary forest is two-storied, lacks tall and big trees and lianas are
absent (Eggeling 1947). The forest is dominated by an even-aged growth of
Maesopsis eminii which forms 50-80% of the canopy (Paterson 1991). Calconcoba
schweinfurthii is the dominant species in the understorey. This site was
mechanically logged between 1945 and 1947 and by pitsawing between 1990 and
2000 (Babweteera et al. 2000). Sixty-seven phorophyte individuals were sampled
from this site.
4.3. Results
4.3.1 Floristic composition
A total of 129 taxa of foliicolous lichens and lichenicolous fungi belonging to 32
genera and 16 families were recorded from Budongo Forest (Fig. 4.5). Of these
125 were identified to the species level, one species was further identified to
variety level (Strigula nemathora var. nemathora & S. nemathora var. hypothelia).
Four were identified to the genus level only (Calenia sp., Coenogonium sp.,
69
Diversity of Foliicolous Lichens in Budong Forest, Uganda
Opegrapha sp. and Biatora sp.). Two species belonging to the genera
Chroodiscus and Tricharia were found to be new to science. For the sake of
simplicity, for the analysis of various parameters, all subspecific taxa and taxa
identified to a genus level were treated as species. The foliicolous lichen and
lichenicolous fungi species recorded from Budongo Forest is presented in
Appendix 6.
120
Number of taxa
100
80
Species
60
Genera
Families
40
20
0
Young
secondary
Swamp
Primary climax
Old secondary
Fig. 4.5 Number of families, genera & species in the four forest types of Budongo
About 95 % of the species in Budongo Forest were typically foliicolous, 3 % were
lichenicolous fungi growing on foliicolous lichens and 1.5 % was facultative
foliicolous species and 0.8 % was ubiquitous species (Fig. 4.6).
Typically foliicolous
Lichenicolous
Facultative
Ubiquatous
Fig. 4.6 Proportion of typical, facultative, ubiquitous foliicolous lichens and
lichenicolous lichens
70
Diversity of Foliicolous Lichens in Budong Forest, Uganda
In the young secondary forest type, 100 species, 29 genera and 14 families were
recorded making this forest type the richest in terms of generic and species
diversity. With 96 species, 27 genera and 12 families, the swamp forest type is the
second diverse. In the primary climax 82 species, 24 genera and 14 families were
recorded. The old secondary forest is comparatively the poorest both in the
number of families (12), genus (17) and species (61). The distribution of foliicolous
lichens and lichenicolous fungi in the four forest types of Budongo is presented in
Appendix 7.
The family Pilocarpaceae is the most dominant in the number of genera (10
genera) and species (28 species). In the number of species, the family Porinaceae
is the second dominant with 26 species. The family Gomphillaceae possessed 16
species and 5 genera. The families Coenogoniaceae and Strigulaceae both
possessed 14 species and 1 genus each. Nine species and 2 genera were
recorded in the family Roccellaceae. Seven species and 3 genera were recorded
in the family Asterothyriaceae. In the family Thelotremataceae one genus and
three species were recorded. The families Arthoniaceae and Aspidotheliaceae
each possessed two species and one genus. The families Coccocarpiaceae,
Microthyriaceae, Bacidiaceae and Lyrommataceae each possessed one species.
Fig. 4.7 presents the number of genera and species in each family in the four
forest types of Budongo. In the primary climax forest type, the family Porinaceae
had the highest species numbers (21 species), followed by Pilocarpaceae (17
species), Strigulaceae (10 species), Coenogoniaceae and Gomphillaceae (8
species), Roccellaceae (4 species), Asterothyriaceae, Ramalinaceae, and
Thelotremataceae
(3
species)
and
Arthoniaceae,
Aspidotheliaceae,
Lyrommataceae and Microthyriaceae had 1 species each. Pilocarpaceae is the
family with the highest number of genera (8 genera), followed by Gomphillaceae (4
genera), Asterothyriaceae and Porinaceae (2 genera), the rest of the families had
one genus each.
In the swamp forest type, Pilocarpaceae had the highest species number (20
species), followed by Porinaceae (19 species), Strigulaceae (14 species),
Coenogoniaceae (13 species), Gomphillaceae (10 species) Roccellaceae (7
species);
Asterothyriaceae
(4
species),
Ramalinaceae
(3
species),
71
Diversity of Foliicolous Lichens in Budong Forest, Uganda
Thelotremataceae
(2
species),
and
Arthoniaceae,
Aspidotheliaceae
and
Lyrommataceae each with one species. In terms of generic diversity, the family
Pilocarpaceae had the highest number of genera (8 genera), followed by
Gomphillaceae with 4 genera, Asterothyriaceae with 3 genera, Porinaceae and
Roccellaceae
with
Aspidotheliaceae,
2
genera
each,
Coenogoniaceae,
and
the
families
Lyrommataceae,
Arthoniaceae,
Ramalinaceae,
Strigulaceae and Thelotremataceae had one genus each.
In the old secondary forest the family Porinaceae possessed the highest number
of species (17 species). The family Strigulaceae is represented by 12 species,
Pilocarpaceae,
Coenogoniaceae
and
Roccellaceae
by
7
species
each,
Ramalinaceae by 3 species and Gomphillaceae by 2 species. The families
Arthoniaceae,
Asterothyriaceae,
Lyrommataceae,
Bacidiaceae
and
Microthyriaceae each possessed one species. The family Pilocarpaceae had 4
genera, Porinaceae and Roccellaceae 2 genera each and the families
Arthoniaceae, Asterothyriaceae, Bacidiaceae, Coenogoniaceae, Gomphillaceae,
Lyrommataceae, Microthyriaceae, Ramalinaceae and Strigulaceae had one genus
each. The family Thelotremataceae which was represented in the other three
forest types is not represented in the old secondary forest type.
The species rich family in the young secondary forest is Porinaceae (23 species),
and it was followed by Pilocarpaceae (18 species). Thirteen species were
recorded in the family Gomphillaceae, 12 species in Strigulaceae, 11 species in
Coenogoniaceae, 7 species in Roccellaceae, 6 species in Asterothyriaceae, 2
species in Thelotremataceae, and 1 species in Arthoniaceae, Aspidotheliaceae,
Bacidiaceae, Coccocarpiaceae, and Lyrommataceae. In the number of genera, the
family Porinaceae is the richest with 9 genera and Gomphillaceae is the second
with 5 genera. The family Asterothyriaceae is represented by 3 genera,
Porinaceae and Roccellaceae by 2 genera each and the remaining families are
represented by one genus each.
72
Diversity of Foliicolous Lichens in Budong Forest, Uganda
Young sec. Species
Porinaceae
Young sec. Genus
Pilocarpaceae
Swamp Species
Gomphillaceae
Swamp Genus
Primary Species
Primary Genus
Strigulaceae
Coenogoniaceae
Old sec. Species
Roccellaceae
Old sec. Genus
Asterothyriaceae
Thelotremataceae
Ramalinaceae
Lyrommataceae
Coccocarpiaceae
Aspidotheliaceae
Arthoniaceae
Bacidiaceae
Microthyriaceae
0
5
10
15
20
25
No. of taxa
Fig. 4.7 Number of species and genera of foliicolous lichens per family per forest
type of Budongo Forest
4.3.2 Species frequency
The frequency occurrences of the foliicolous lichens in the samples of the four
forest types of Budongo Forest are presented in Fig. 4.8. In all study sites of
Budongo Forest, the rare species constituted more than 57% of the whole species
and 11-21% of the species were occasional. These two species groups constituted
more than 80% of the species in the primary, swamp and young secondary forest
types and about 71% of the species in the old secondary forest type.
Comparatively the rare species in the old secondary forest type were fewer
(57.4%) than those in the primary (64.2%), swamp (69.8) and young secondary
forests (66%). Similarly, there were more dominant species (9.8%) in the old
secondary forest type than in the other forest types which have less than 5%
dominant species.
73
Diversity of Foliicolous Lichens in Budong Forest, Uganda
100%
90%
80%
70%
60%
50%
40%
30%
20%
10%
0%
Rare
Occasional
Less frequent
Frequent
Very frequent
Dominant
Primary
Swamp
Old secondary
Young
secondary
Fig. 4.8 Frequency distribution of species in the four forest types of Budongo
Forest
In the primary forest type Coenogonium dilucidum, Porina radiata, P. epiphylla and
Mazosia melanopthalma were the dominant species. Mazosia rotula, Porina
nitidula and Strigula phyllogena were the most frequent species while Porina
semicarpi was the only frequent species. The less frequent species were Porina
sphaerocephala, P. alba, Brasilicia foliicola, Byssolecania deplanata, Strigula
microspora, S. nitidula and S. smaragdula. The occasional species were
Byssolecania fumosonigricans, B. hymenocarpa, Bacidina mirabilis, Calopadia
fusca, Coenogonium pocsii, C. subluteum, Echinoplaca pellicula, Lyromma
nectandrae, Porina cupreola var. cupreola, P. epiphylloides, P. kamerunensis, P.
rubentior, Sporopodium leprieurii and Strigula nemathora var. hypothelia. The rare
species were Coenogonium fallaciosum, Arthonia lividula, Aspidothelium fugiens,
Asterothyrium microsporum, A. monosporum, Bapalmuia ivoriensis, B. palmularis,
Bacidina
apiahica,
subpolychromum,
Bacidina
simplex,
Byssoloma
chlorinum,
Byssoloma
Brasilicia dimerelloides, Byssolecania variabilis, Calenia
depressa, Calenia graphidea, Calenia bullatinoides, Coenogonium geralense, C.
pannosum, C. subdilucidum, C. usambarense, Chroodiscus australiensis,
Chroodiscus
kakamegensis
sp.nov.,
Chroodiscus
verrucosus,
Fellhanera
bouteillei, F. submicrommata, Gyalectidium filicinum, G. imperfectum, Gyalidea
epiphylla,
Lichenopeltella
epiphylla,
Mazosia
dispersa,
M.
phyllosema,
Phylloblastia pocsii, Porina cf. triseptata, P. conica, P. leptosperma, P. rubescens,
74
Diversity of Foliicolous Lichens in Budong Forest, Uganda
P. rufula, P. sphaerocephaloides, P. subpallescens, Strigula janeriensis, S.
macrocarpa, S. multipunctata, S. obducta, S. pilocarpoides, S. subtilissima,
Sporopodium antonianum, Tapellaria nigrata, Tricharia nigriuncinata sp. nov., T.
vainioi, Trichothelium africanum, Trichothelium pauciseptatum, T. alboatrum, and
T. epiphyllum.
In the swamp forest Porina epiphylla, Strigula phyllogena, and Coenogonium
dilucidum were the dominant species. Mazosia rotula, Porina alba, P. radiata, P.
rubentior and P. nitidula were very frequent. The frequent species were Porina
semicarpi, Strigula nitidula, S. smaragdula, Mazosia melanopthalma and Porina
sphaerocephala. The less frequent were Porina conica, Strigula nemathora var.
hypothelia, S. microspora, S. obducta and Sporopodium leprieurii. Occasionals
were Porina leptosperma, P. epiphylloides, P. rubescens, P. rufula, Brasilicia
foliicola, Byssolecania deplanata, Gyalectidium filicinum, Lyromma nectandrae,
Strigula
nemathora var.
nemathora,
Tricharia
vainioi,
and
Trichothelium
pauciseptatum. The rare species were Arthonia orbygniae, Aspidothelium
geminiparum, Asterothyrium microsporum, A. monosporum, Bacidina apiahica, B.
mirabilis, B. pallidocarnea, Bapalmuia ivoriensis, Bapalmuia palmularis, Brasilicia
dimerelloides,
Byssolecania
fumosonigricans,
Byssolecania
hymenocarpa,
Byssoloma chlorinum, Byssoloma leucoblepharum, Calenia aspidota, Calenia
depressa, Calenia graphidea, Calopadia fusca, Calopadia puiggarii, Chroodiscus
australiensis, Chroodiscus verrucosus, Coenogonium barbatum, C. fallaciosum, C.
geralense, C. lisowskii, C. pocsii, C. siquirrense, C. subdilucidum, C.
subfallaciosum, C. subluteum, C. usambarense, C. zonatum, Echinoplaca
pellicula,
Fellhanera
africana,
F.
rhaphidophylli,
F.
subfuscatula,
F.
submicrommata, Gyalectidium caucasicum, G. eskuchei, G. imperfectum,
Gyalidea epiphylla, Lichenopeltella epiphylla, Loflammia epiphylla, Mazosia
dispersa, M. paupercula, M. phyllosema, Opegrapha epiporina, O. phylloporinae,
Porina mazosoides, P. sphaerocephaloides, P. subpallescens, Psorotheciopsis
patellarioides, Sporopodium antonianum, S. phyllocharis, S. pilocarpoides, Strigula
antillarum, Strigula janeriensis, Strigula macrocarpa, Strigula maculate, Strigula
multipunctata, Strigula schizospora, Strigula subtilissima, Tricharia nigriuncinata
sp. nov., Trichothelium africanum, Trichothelium alboatrum and Trichothelium
epiphyllum.
75
Diversity of Foliicolous Lichens in Budong Forest, Uganda
In the old secondary forest type the dominant species were Porina epiphylla, P.
kamerunensis, P. nitidula, P. rubentior, Mazosia melanopthalma and Strigula
phyllogena. Porina cupreola var. cupreola and Strigula nitidula were very frequent
species. The frequent
species
were
Porina
radiata, P.
rubescens, P.
sphaerocephala, Strigula nemathora var. hypothelia and Strigula smaragdula.
Bacidina apiahica, Byssolecania
hymenocarpa, Strigula
multipunctata, S.
microspora and Porina rufula were the less frequent species. The occasional
species were Brasilicia foliicola, Byssoloma chlorinum, Coenogonium dilucidum,
Lyromma nectandrae, Opegrapha epiporina, O. phylloporinae and Porina
semicarpi. The rare species were Arthonia lividula, Asterothyrium microsporum,
Bacidina mirabilis, Bacidina simplex, Brasilicia dimerelloides, Byssolecania
deplanata, B. fumosonigricans, B. subdiscordans, Coenogonium geralense, C.
pocsii, C. siquirrense, C. subluteum, C. usambarense, C. zonatum, Fellhanera
submicrommata, Gyalectidium filicinum, G. imperfectum, Lichenopeltella epiphylla,
Mazosia phyllosema, M. rotula, Opegrapha mazosiae, Porina alba, P. conica, P.
leptosperma, P. subpallescens, Strigula janeriensis, S. macrocarpa, S. nemathora
var. nemathora, S. obducta, S. schizospora, S. subtilissima, Trichothelium
africanum, Trichothelium pauciseptatum and T. epiphyllum.
In the young secondary forest type Strigula smaragdula is the only dominant
species. Porina nitidula, P. rubentior, Strigula nemathora var. hypothelia and S.
nitidula were the very frequent species. The frequent species were Strigula
phyllogena, Coenogonium dilucidum, Mazosia rotula and Porina epiphylla. The
less frequent species were Porina radiata, P. sphaerocephala, Strigula microspora
and Echinoplaca pellicula. The occasional species were Bacidina apiahica,
Byssolecania deplanata, B. hymenocarpa, Byssoloma chlorinum, Calenia
depressa, C. graphidea, Fellhanera submicrommata, Gyalectidium filicinum, G.
imperfectum, G. microcarpum, Lyromma nectandrae, Mazosia melanopthalma,
Porina cupreola var. cupreola, P. epiphylloides, P. kamerunensis, P. leptosperma
P.
rubescens,
P.
sphaerocephaloides,
P.
subpallescens,
and
Strigula
multipunctata.
76
Diversity of Foliicolous Lichens in Budong Forest, Uganda
The frequency of occurrences of foliicolous lichens in Budongo Forest and the
primary, swamp, old secondary and young secondary forest parts are presented in
Appendices 8, 9, 10, 11 and 12 respectively.
4.3.3 Foliicolous lichens from canopy trees
In the sampling site of the primary climax forest type, a recently fallen tree of Celtis
durandi reaching a height of 35 m was encountered. Leaves carrying foliicolous
lichens were collected from the branches at a height of 20 to 35 m. Only Strigula
smaragdula was recorded from the leaves. This species covered upto 80% of the
leaf areas. In addition, a recently fallen tree of Ficus lutea was encountered in a
place called Susungiru, about 8 km from the Budongo Forest project office. The
following foliicolous lichens were recorded from the leaves of this canopy tree:
Asterothyrium monosporum, Asterothyrium pittieri, Asterothyrium rotuliforme,
Calenia aspidota, Psorotheciopsis patellarioides, Psorotheciopsis varieseptata,
Strigula antillarum, and Strigula smaragdula. From this forest site 68 species of
foliicolous lichens were recorded from the understorey.
4.3.4 New species and new records of foliicolous lichens
The checklist of lichens and lichenicolous fungi of Uganda (Feuerer 2007) listed
362 species. Out of these 29 species are foliicolous lichens. Sixteen of the species
recorded in this study have already been included in the checklist. The remaining
108 species are new records for Uganda. The list of new records of foliicolous
lichens is presented in Appendix 6.
4.3.4.1 Species new to science
Two species of foliicolous lichens belonging to the family Gomphillaceae and
Thelotremataceae were found to be new to science. These are Tricharia
nigriuncinata sp. nov. and Chroodiscus kakamegensis sp. nov.
1. Tricharia nigriuncinata sp. nov. (Gomphillaceae). Fig. 4.9
77
Diversity of Foliicolous Lichens in Budong Forest, Uganda
This new species of Tricharia is distinguished from all other species of the genus
by the presence of hooks on the sterile setae (see arrow in Fig. 4.8).
Fig. 4.9 Tricharia nigriuncinata
Specimen examined: Budongo Forest, 01043’22.9 N, 031031’45.3 E, 900 m,
epiphyllous on Argomuellera macrophylla in the primary forest type, 2005,
Kumelachew 16, 65, 66, 71, 75 (KOBL).
2. Chroodiscus kakamegensis sp. nov.
Chroodiscus kakamegensis is a facultative lichenicolous lichen growing on Porina
epiphylla. It has been collected from Godere, Budongo and Kakamega forests. A
brief description of the species was provided in section 3.3.3.1
Specimen examined: Budongo Forest, 01043’22.9 N, 031031’45.3 E, 1082 m,
epiphyllous on Argomuellera macrophylla, Kumelachew 96 (KOBL)
4.3.4.2 Interesting records of foliicolous lichens
From the foliicolous lichen collection of Budongo Forest, the following interesting
records were obtained.
78
Diversity of Foliicolous Lichens in Budong Forest, Uganda
1. Brasilicia foliicoloa (Pilocarpaceae) Fig. 4.10
The apothecia of the specimens cited below grew marginally hypophyllous which
is untypical for Brasilicia foliicola.
Fig. 4.10 Brasilicia foliicola (note marginally hypophyllous apothecia)
Specimen examined: Budongo Forest, 01043’22.9 N, 031031’45.3 E, 1082 m,
epiphyllous on an unidentified species of tree in the primary forest, 2005,
Kumelachew 92, 93 (KOBL).
2. Gyalidea epiphylla (Asterothyriaceae)
The specimen cited below had smaller ascospores (10 x2.5 µm) than the typical
species whose ascospore size is 13-25x3.5-4.5 µm (Vězda 1966).
Specimen examined: Budongo Forest, 01042’46.6 N, 031032’.31.7 E, 1038 m,
epiphyllous on unidentified species of Sapindaceae in the young secondary forest
type, 2005, Kumelachew 115 (KOBL).
79
Diversity of Foliicolous Lichens in Budong Forest, Uganda
3. Calenia sp. (Gomphillaceae) Fig. 4.11
The collection of Calenia cited below has got pruinose apothecia, a single
muriform, ellipsoid ascospore per ascus and a prosoplectenchymatous excipulum.
This collection is assumed to be a new species of Calenia but the material is
scanty for a proper description.
Fig. 4.11 Calenia sp.
Specimen examined: Budongo Forest, Royal Mille, 01042’46.6 N, 031032’.31.7 E,
1038 m, epiphyllous on unidentified species, 2005, Kumelachew 117 (KOBL).
Difficult specimens
1. unknown taxon of Pilocarpaceae (Fig. 4.12)
A single specimen belonging to the family Pilocarpaceae was difficult to identify
even to the genus level. It had centrally continuous and marginally dispersed
thallus, and black apothecia (Fig. 4.12a), single muriform ascospore per ascus,
branched and anastomised pharaphyses, tubular campylidia (Fig. 4.12b) and
simple and bacilliform conidia with thickened ends (Fig. 4.12c). Such types of
conidia are unknown in the foliicolous members of Pilocarpaceae.
80
Diversity of Foliicolous Lichens in Budong Forest, Uganda
a
b
c
Fig. 4.12 An unknown specimen in Pilocaraceae a) thallus with apothecia (arrows),
b) thallus with campylidia (arrows), c) conidia
Specimen examined: Budongo Forest, Royal Mille, 01042’46.6 N, 031032’31.7,
1038 m, epiphyllous on an unidentified species of Rubiaceae, 2005, Kumelachew
118 (KOBL).
2. Coenogonium sp.
Several collections of the genus Coenogonium were difficult to identify. The recent
worldwide key for Coenogonium (Rivas-Plata et al. 2006) doesn’t have sufficient
information for the identification our collection. It is highly likely that some of these
specimens could represent new taxa of Coenogonium. This shows that further
investigation in the African Coenogonium is required.
81
Diversity of Foliicolous Lichens in Budong Forest, Uganda
3. aff. Biatora sp.
Three corticolous lichen specimens belonging to the family Bacidiaceae and
growing facultatively on margins of living leaves were difficult to identify. They
have simple and cylindrical ascospores and are close to the genus Biatora.
Specimen examined: Budongo Forest, Royal Mille, 01042’28.7 N, 031032’33.5 E,
1050 m, epiphyllous on Rawsonia lucida, 2005, Kumelachew 192, 193,
207(KOBL)
4.3.2 Alpha-diversity
4.3.2.1 Mean species number
The mean number of species recorded per sample was 10.5 for the primary forest
type, 11.3 for the swamp forest type, 10.7 for the old secondary forest type and
10.3 for the young secondary forest type (Fig. 4.13). Kruskal-Wallis one-way
analysis of variance test showed absence of significant differences (Chi square =
2.26, p > 0.05) among the four forest types in the mean number of species per
sample.
20
18
Meanspecies number
16
14
12
10
8
6
4
2
0
Primary
Swamp
Old
Young
secondary secondary
Fig. 4.13 Mean number of species per sample per forest type (values are mean ±
SD)
82
Diversity of Foliicolous Lichens in Budong Forest, Uganda
4.3.2.2 Species accumulation curve
The species accumulation curves for the primary, swamp, old secondary and
young secondary forests types of Budongo are presented in Fig. 4.14. The x-axis
of the first graph is scaled by the number of accumulated samples and it compares
species density between the forest types. The x-axis of the second graph is scaled
by the number of individuals and thus compares species richness. The species
accumulation curves for the four forest types did not approach an asymptote, but
the rate of accumulation of species as successively more samples are
accumulated to the total is decreasing.
As can be seen from the species accumulation curves, more species numbers are
expected in the swamp and young secondary forest types than in the primary and
old secondary forest types at all levels of sample accumulation (Fig. 4.13a). More
species were observed in the swamp forest when lower samples were
accumulated. At higher number of sample accumulation, however, more species
were observed in the young secondary forest. The old secondary forest has the
lowest number of species at all level of sample accumulation. The number of
species expected from the species accumulation curves when 22 samples (the
sample size of the old secondary forest type) were pooled is 71.1 for the young
secondary forest type, 70.2 for the swamp forest type, 66.2 for the primary forest
type and 61 species for the old secondary forest type. To see if there is significant
difference in species richness, Magurran (2004) recommended to check if the
observed diversity of the smaller community lies within the 95% confidence limits
of the rarefaction curve of the larger community. Accordingly, the observed
species accumulation curve of the primary forest is within the 95% confidence
intervals of the corresponding species accumulation curves of the swamp and
young secondary forests indicating absence of significant difference. Similarly, the
observed species accumulation curve of the swamp forest is within the 95%
confidence intervals of the young secondary forests. The observed species
accumulation curve of the old secondary forest is within the 95% confidence
intervals of the primary forest but outside the 95% confidence intervals of the
swamp and the young secondary forests indicating absence of significant
difference in species richness between the old secondary and the primary forest
83
Diversity of Foliicolous Lichens in Budong Forest, Uganda
types but the swamp and young secondary forests are significantly more species
richer than the old secondary forest type (Fig. 4.14b).
120
A
Number of species
100
80
60
40
20
0
0
10
20
30
40
50
60
500
600
70
80
No. of samples
120
B
No. of species .
100
80
60
40
20
0
0
100
200
300
400
700
800
No. of individuals
Fig. 4.14 Species accumulation curves for the primary (green), swamp (red) and
old secondary (black) and young secondary (blue) forest types. A) Species
density, B) Species richness
84
Diversity of Foliicolous Lichens in Budong Forest, Uganda
4.3.2.3 Estimation of species richness
The non-parametric species richness estimators for incidence data variously
estimated the species richness of the four forest types of Budongo Forest (Table
4.3). For the primary and young secondary forest types, the Bootstrap estimator
gave the lowest and the second order Jackknife estimator gave the highest
estimate of species richness. The second order Jackknife estimator gave the
highest species richness estimate for the swamp forest type and the MichalisMenten Mean estimator gave the lowest estimate. For the old secondary forest
type, Chao 2 estimator gave the highest estimate and Bootstrap the lowest
estimate of species richness.
Table 4.3. Number of samples, number of individuals and species richness
estimate values for the four forest types of Budongo.
Primary forest
No. of samples
Swamp
forest
Old
secondary
forest
22
Young secondary
forest
41
64
431
725
235
689
81
96
61
100
94.7
105.5
74.4
112.3
Chao 2
103.4±6.8
113.8±9.8
117±30.9
117.8±9.8
Jackknife 1
104.4±6.8
118.6±5.5
87.7±6.9
122.7±5.4
Jackknife 2
117
128.5
107.1
132.6
Bootstrap
91.8
106.6
72.2
111
ICE
104.04±0.03
111.1±0.01
102.3
118.1±0.02
Degree of foliicolous
69.2-88.2%
74.7-91%
52.1-84.5
75.4-90.1
No. of individuals
Sobs
MMMeans
67
lichen collection
Comparison of the number of species observed and the species richness
estimated by the various richness estimators showed that 69.2-88.2% of the
species have been collected from the primary forest, 74.7-91% of the species from
85
Diversity of Foliicolous Lichens in Budong Forest, Uganda
the swamp forest, 52.1-84.5% of the species from the old secondary forest and
75.4-90.1% of the species were collected from the young secondary forests. The
differences between the highest and the lowest species estimators were 15.2
species for the primary forest type, 23 species for the swamp forest type, 44.8
species for the old secondary forest type and 21.6 species for the young
secondary forest type. The big difference in the old secondary forest type is due to
the overestimation of Chao 2 estimator which relies on uniques (species restricted
to one sample only) which accounted for 46% of the whole species in this forest
type.
4.3.2.4 Shannon-Wiener diversity
The Shannon diversity index and evenness values in each forest type are shown
in Table 4.4. Analysis of Variance (ANOVA) of the Shannon diversity values of the
four forest sites showed the presence of significant difference (F-ratio = 3.49,
P<0.05). Fischer’s post hoc comparison test indicated that the old secondary
forest type is significantly different from the other three forest types. There was no
significant difference among the Shannon diversity of the primary, the swamp and
the young forest types. Accordingly, the primary (H’=3.9), swamp (H’=4.0) and
young secondary (H’=4.1) forest types have higher diversity than the old
secondary forest type (H’=3.6). The Shannon evenness values are the same
(J’=0.88) for the primary, old secondary and young secondary forests and slightly
lower in the swamp forest type.
Table 4.4 Shannon-Wiener diversity and evenness index values.
Primary
Swamp
Old
Young
secondary
secondary
Shannon index (H’)1
3.9a
4.0a
3.6b
4.1a
Shannon evenness
0.89
0.88
0.89
0.89
index (J’)
1
Different alphabetical letter designations indicate significant difference (p<0.05) among
Shannon diversity values of the forest types
86
Diversity of Foliicolous Lichens in Budong Forest, Uganda
4.3.3 Beta-diversity and similarity in species composition
Total β-diversity, measured as total species number divided by mean number of
species in samples, along forest types of Budongo Forest is presented in Table
4.5. This index of β-diversity is a measure of the species turnover or the degree of
change in species composition. The young secondary forest had the highest βdiversity (9.8) and therefore high species turnover, followed by the swamp forest
(8.5) and primary forest (7.8) and the old secondary forest has the lowest βdiversity value (5.7) and therefore low species turnover.
Table 4.5 β-diversity along the forest types of Buyangu
Number of
species
(a)
Mean number of
species per sample
(b)
β-diversity
(a/b)
Primary forest
82
10.5
7.8
Swamp forest
96
11.3
8.5
Old secondary forest
61
10.7
5.7
Young secondary forest
100
10.2
9.8
Table 4.6. Sørenson’s index of similarity among the four forest types
Primary
Swamp
Old secondary
Primary
-
Swamp
0.77
-
Old secondary
0.7
0.68
-
Young secondary
0.74
0.75
0.67
The similarity in foliicolous lichen species composition, as measured by
Sørenson’s index of similarity, shows generally a high similarity among the four
forest types of Budongo with a mean Sørenson’s similarity index of 0.72. The
highest species composition similarity among the forest types was observed
between the primary and swamp forest types (Ss=0.77) followed respectively by
the young and swamp forest types (Ss=0.75), the primary and young secondary
87
Diversity of Foliicolous Lichens in Budong Forest, Uganda
forest types (Ss=0.74), the primary and old secondary forest types (Ss=0.7), the old
secondary and swamp forest types (Ss=0.68) and the least similarity was observed
between the young and old secondary forest types (Ss= 0.67) (Table 4.6).
4.3.4 Ordination
Fig. 4.15 shows a graphic representation of the first two axes of a DCA ordination.
The first axis of the ordination had eigenvalue of 0.401 contributing to 7.3% of the
total variation. The second axis with eigenvalue of 0.217 contributed to 4% of the
variation. The third and fourth axes had eigenvalues of 0.180 and 0.163
respectively, each contributing to less than 4% of the total variation. Therefore,
most of the variation in the DCA ordination is explained by the first axis.
Fig. 4.15 DCA plot of samples of Budongo Forest. Green circles = samples from
swamp, yellow squares = samples from primary, black squares = samples from old
secondary, and red circles = samples from young secondary forest types.
Along the first DCA axis, samples with low first axis scores are from the closed
forest sites with dominating shady understorey micrositic conditions and they are
arranged on the left side of the axis. Samples with high first axis scores are from
open forest sites where light gap microsite conditions dominate and are arranged
88
Diversity of Foliicolous Lichens in Budong Forest, Uganda
on the right side of the axis. Most of the samples from the swamp, primary forest
and old secondary forest sites are located on the left side of the first ordination
axis. While few samples of the young secondary forest site are distributed on the
left side of the first DCA axis, the majority of the samples being distributed on the
right side of this axis. These distribution patterns indicate that vegetation type
(degree of anthropogenic disturbance; in the terminology of Lücking 1997b) seems
to be the factor for the variation in the distribution of the samples.
Fig. 4.16 DCA plot of foliicolous lichen species of Budongo Forest. Only species
with high occurrences are shown. Green circles = species of undisturbed primary
forest, light green circles = species of primary & old growth forest, brown squares
= species of semi-open forest, blue circles = species of open forest (forest
margin), black squares = species of open to exposed forest, red circles = species
of exposed vegetation, x = species with wide amplitude. For acronyms, refer to
Appendix 6.
89
Diversity of Foliicolous Lichens in Budong Forest, Uganda
For the interpretation of the species ordination (Fig. 4.16), the environmental index
values of foliicolous lichens (Lücking 2000b, with addition of my personal
observation) with respect to vegetation type (degree of anthropogenic disturbance)
and light regime (microsite), was first determined. Species with high scores on the
first DCA axis are canopy species distributed in the open to exposed forest parts.
Species with low scores are from shady understorey and light gap of closed
forests and semi-open forest.
4.3.5 Phorophytes
Argomuellera macrophylla, Cynometra alexandri, Trichilia emetica, Maranthacloa
sp., Rawsonia lucida, Rinorea ardisiaeflora, Hippocratea sp., Antiaris toxicaria,
Chrysophyllum albidum, Campylospermum sp., Memecylon jasminoides, Teclea
nobilis,
Pterygota
mildbraedii,
Aframomum
sp.,
Oxyanthus
lepidus,
Tabernaemontana holstii, Trichilia rubescens, Celtis mildbraedii, Chionanthus
mildbraedii, Funtumia africana, Blighia unijugata, Coffea canephora, Conarus
longistipitatus, Dracaena fragrans, Lasiodiscus mildbraedii, Ouratea densiflora,
Schefflera sp., Alchornea florubinda, Khaya anthotheca, Macaranga sp., Citropsis
articulate,
Melianthus
westii,
Turreantus
africanus,
Agelaea
ugandensis,
Commelina sp., Pollia condensate, Acalypha sp., Leptaspis cochleata, Uvariopsis
congensis, Lychnodiscus cerospermus, Bequaertiodendron oblanceolatum, Kigelia
africana, Strychnos sp., Ficus asperifolia, Mitragyna stipulosa and some
unidentified species in the family Euphorbiaceae, Rubiaceae, Sapindaceae,
Annonaceae, Sapindaceae and ferns were the phorophytes that supported
foliicolous lichens in Budongo Forest. Argomuellera macrophylla was the
phorophyte that supported the most species (75 species) and the highest record
(229 records of foliicolous lichens). Cynometra alexanderi supported 5 species
and 124 records of foliicolous lichens, Trichilia emetica supported 43 species and
43 records of foliicolous lichens, Maranthacloa sp. supported 39 species and 9
records of foliicolous lichens, Rawsonia lucida supported 34 species and 47
records of foliicolous lichens and Rinorea ardisiaeflora supported 33 species and
50 records of foliicolous lichens.
90
Diversity of Foliicolous Lichens in Budong Forest, Uganda
4.4 Discussion
4.4.1 Sample size sufficiency
Sufficiency of sampling can be evaluated using species accumulation curves and
by comparing the values of various species richness estimators. Sampling is said
to be sufficient when the species accumulation curve reach a horizontal asymptote
(Soberón & Llorente 1993). The species accumulation curves for the observed
species of the four forest types of Budongo did not reach a horizontal asymptote
indicating more species could be recorded with additional sampling effort. Soberón
& Llorente (1993) have indicated that in evaluating species accumulation curves,
the rate of accumulation of new species should be compared. The rate of
accumulation of new species as more samples were pooled has very much
reduced for the primary, swamp, and young secondary forest types and less
reduced for the old secondary forest type.
According to the estimates of the various species richness estimators, 69-88% of
the species from the primary forest part, 75-91% from the swamp forest, 52-85%
from the old secondary forest and 75-90% from the young secondary forest were
collected in this study. According to the report of Heck et al. (1975) which
considers collection of 50% to 75% of the total species richness of an area as
satisfactory, the numbers of foliicolous lichen species collected from the four study
sites are quite satisfactory.
4.4.2 Diversity of foliicolous lichen families and genera in the four forest
types
In terms of family diversity the young secondary and the primary forest types are
comparatively more diverse than the swamp and the old secondary forest types.
The families Aspidotheliaceae, Thelotremataceae and Verrucariaceae were not
represented in the old secondary forest type. The families Aspidotheliaceae and
Verrucariaceae were not represented in the swamp forest. In terms of generic
diversity, the young secondary forest is the most diverse and the old secondary
forest is the least diverse. The genera Aspidothelium, Bapalmuia, Calenia,
Calopadia, Chroodiscus, Echinoplaca, Gyalidea, Loflammia, Psorotheciopsis,
91
Diversity of Foliicolous Lichens in Budong Forest, Uganda
Phylloblastia, Tapellaria and Tricharia were not represented in the old secondary
forest. Most of these genera are represented in the primary, swamp and young
secondary forest types.
4.4.3 Species richness in the four forest types of Budongo
At all levels of sample accumulations, the species accumulation curves showed
higher estimate of species richness for the young secondary and swamp forests
than for the primary and old secondary forest types. When comparing the absolute
number of species, the young secondary forest type is the most species rich,
followed respectively by the swamp forest, the primary forest and the old
secondary forest is the least species rich. Observation of the species accumulation
curves and their 95% confidence intervals, however, shows that the young
secondary and the swamp forest types are not significantly different in species
richness. Considering this statistical significance, the young secondary and the
swamp forest are the most species rich forest type; the primary forest is the
second species rich and the old secondary forest type is the least species rich
forest type.
Alpha diversity, as measured by the species accumulation curves, species
richness estimators and Shannon index, and β-diversity of foliicolous lichens were
found to be high in the young secondary and swamp forest types. The primary
forest assumes an intermediate position and the old secondary forest has the
lowest α-diversity and β-diversity of foliicolous lichens. The similarity in foliicolous
lichen species composition of the four forest types of Budongo is mainly due to
similar microclimatic conditions. Shady understorey and transition to light gap
species accounted for 62% of the species in the primary, 60% in the swamp, 58%
in the old secondary and 55% of the species in the young secondary forest.
Previous studies on the diversity of foliicolous lichens in the Neotropics (Lücking
1992b, Lücking 1998b) observed high species richness in undisturbed forests and
a reduced richness in disturbed and secondary forests. Our study, however,
showed that secondary forests could also support similar or even higher foliicolous
lichen diversity than undisturbed primary forests. The high diversity in the swamp
and young secondary forest is due to occurrence of the whole microsite habitats
92
Diversity of Foliicolous Lichens in Budong Forest, Uganda
which are suitable for the growth of foliicolous lichens. In addition to the shady
understorey
and
light
gap
microsite
species,
canopy
specialists
(e.g.
Asterothyrium pittieri, A. rotuliforme, Psorotheciopsis patellaroides, Canlenia
aspidota) are also recorded in the understorey of the young secondary forest type.
The most recent selective logging by pitsawing in the period between 1990 and
2000 (Babweteera et al. 2000) might have contributed for the appearance of such
species in the understorey of this forest type. Lücking (1998d) postulated that
diversity of microsites with different microclimate provoked by strong gap
dynamics is important for the diversity of foliicolous lichens.
The finding from this study is in line with the Intermediate Disturbance Hypothesis
(Connell 1978) which states that species diversity in a landscape is highest in
areas with an intermediate level of disturbance. The effect of disturbance on
foliicolous lichen diversity is dependent on the frequency and intensity of
disturbance. When the intensity of disturbance is high leading to wide canopy
openings, the increasing light intensity and the reduced atmospheric moisture
affect the shady understorey and the transition to light gap species thereby
reducing the diversity of foliicolous lichens. Under moderate level of disturbance,
for example small scale logging by pitsawing, partial canopy openings could
enhance the establishment of light demanding species without seriously
jeopardizing the shade loving species.
4.4.4 β-diversity
Total β-diversity, measured by the total number of species divided by the mean
species number per sample, is relatively high in the young secondary forest (βdiversity = 9.8) with a relatively higher species turnover and low in the old
secondary forest (β-diversity = 5.7) with a relatively lower species turnover. The
high Sørenson indices (0.67-0.77) among the four forest types are evidence for a
low species turnover and therefore low β-diversity in Budongo Forest. The low βdiversity in turn is an indication of comparable microenvironmental conditions in
the forest types.
93
Diversity of Foliicolous Lichens in Budong Forest, Uganda
4.5 Conclusion
•
The foliicolous lichen species richness of Budongo Forest is considerably
high.
•
Diversity of foliicolous lichens in Budongo Forest is high not only in the
primary forest parts, but in the young secondary forests as well.
•
High foliicolous lichen diversity in Budongo Forest is due to the availability
in close proximity of forest types with different succession stages and
disturbance history.
•
The high proportion (> 55% of species) of shady understorey and transition
to light gap species in the four forest types is due to closed forest canopy
which is indicative of minimal forest disturbance.
94
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Chapter 5. DIVERSITY OF FOLIICOLOUS LICHENS IN
KAKAMEGA FOREST, KENYA
5.1 Study area
5.1.1 Location and physiography
Kakamega Forest is located in Shinyalu Division of Kakamega District in the
Western Province of Kenya. It is situated about 40 km northwest of Lake Victoria
between 0010’ and 0021’ N latitudes and 34047’ and 34058’ E longitudes (Fig. 5.1).
Fig.5.1 Map of Kenya showing the location of Kakamega Forest (red square).
Source: (www.village-sanctuary.com)
95
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
The Kakamega District is situated in the Lake Victoria Basin and most of the forest
lies on flat to undulating terrain with only few steep hills including Buyangu and
Lirhanda (Blackett 1994). The forest has an area of 240 km2 though only
approximately 100 km2 still consists of indigenous forest (Fashing & Gathua 2004).
The remaining portion of the reserve consists of plantations, tea field, and
grasslands (Wass 1995). The official forest boundary of Kakamega Forest lies
between 1460 and 1765 m a.s.l. (Lung & Schaab 2006). Two major rivers pass
through the forest, each with several tributaries, particularly in the eastern blocks
of the forest (Kokwaro 1988). In the northern section of the forest is the Isiukhu
River, which rises in the North Nandi Forest and the Nandi Escarpment. The
southern section of the forest is dissected by the Yala Rivers, together with its
many tributaries with sources mainly in the Tinderet Forest and South Nandi
Forest.
Kakamega Forest covers 8,500 ha of a main forest block surrounded by five forest
fragments of various sizes (130-1,400 ha): Malava and Kisere in the north, and
Yala, Ikuywa and Kaimosi in the south (Farwig et al. 2006) (Fig. 5.2).
5.1.2 Geology and Soil
Kakamega Forest is located in the Lake Victoria Basin whose underlying bedrock
is the Precambrian rock (Lovett & Waser 1993). The Precambrian rock is
composed of basalt, phenolites and ancient gneiss which are associated with goldbearing quartz veins (Blackett 1994). The underlying rock is overlain by soils of
low fertility ferralo-chromic/orthic acrisols, which are well-drained, deep, heavily
leached, medium to heavy texture clay-loams and clays, usually with pH below 5.5
(Blackett 1994). The soils to the east and north-east of the forest are humic
cambisols and acrisols (Blackett 1994, Tattersfield et al. 2001, Glenday 2006). To
the south-east of the forest, there is an area of more fertile nitosols (Blackett1994).
Musila (2007) identified four soil classes in Kakamega Forest: Ferralsols (in
Salazar and Kisere), Cambisols (in Isecheno, Kaimosi and Yala), Phaeozems (in
Ikuywa), and Lixisols (in camp site).
96
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Fig. 5.2. Satellite image (Landsat 7 ETM+, 05 Feb 2001) of Kakamega Forest and
its fragments (source: BIOTA-E02, G. Schaab).
97
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
A
B
Fig. 5.3. Aerial images of Malava (A) and Kisere (B) forests. Source: Dr.
Rainer Steinbrecher, BIOTA East Africa
98
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
5.1.3.Climate
The area around Kakamega Forest has one of the highest levels of annual rainfall
in Kenya. Rainfall in Kakamega is bimodal, the long rains falling in April and May
and the short rains falling in September and October. The dry season is from the
end of December to February. The Forest Department records rainfall at Isecheno
forest station and the average annual rainfall between the period 1982 and 2006
was between 1343 and 2638 mm (Fig. 5.4). The average annual temperature of
the forest is between 10.6 and 27.7 0C and the average monthly maximum
temperature ranges from 18 to 290C while the corresponding minimum
temperature varies from 4 to 210C (Muriuki & Tsingalia 1990).
300
Rainfall (mm
250
200
150
100
50
0
J
F
M
A
M
J
J
A
S
O
N
D
Month
Fig. 5.4. Rainfall data from Isecheno meteorological station for the periods
between 1982 and 2006. Source: BIOTA East Africa
5.1.4. Vegetation, flora and plant communities
The vegetation of Kakamega Forest contains a mosaic of primary rainforest,
secondary forests of different seral stages, swamp and riverine forest, selectively
logged forest, plantations of indigenous and exotic tree species, natural glades,
and clearings made following human disturbances (Mutangah et al. 1994,
Tattersfield et al 2001).
99
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
The forest type of Kakamega has been classified differently by various authors:
upland rainforest (Greenway 1973), transitional rainforest (White 1983), tropical
rainforest (Beentje 1990), mid-altitudinal tropical rainforest (Bleher et al. 2005) and
dry peripheral semi-evergreen Guineo-Congolian transitional rainforest (Althof
2005). Kokwaro (1988) described Kakamega Forest as the easternmost relic of
the equatorial forests that stretch across the Congo basin and the only tropical
rainforest of the Guineo-Congolian type found in Kenya. It occupies a transitional
position between the Guineo-Congolian lowland forests and the afromontane
forests of the highlands to the west of the Rift Valley (Blackett 1994). Floristically,
the forest consists of species from the Guineo-Congolian floral region, from the
Afromontane floral region and species which fall neither in the former nor in the
latter regions, and are thus transitional.
Several authors documented the flora of Kakamega Forest.
Kokwaro (1988)
recorded 147 species of woody plants and 227 species of herbaceous plants.
Blackett (1994) recorded 132 tree species. Althof (2005) recorded 112 species of
trees, 62 species of shrubs, 58 species of climbers and 165 species of herbaceous
plants (including ferns).
Among the 212 woody species recorded in Kakamega Forest (Althof 2005), 41%
were Guineo-Congolian origin, 33% were related to the Afromonatne forest system
and 26% were transitional species. The Guineo-Congolian species include
Pouteria (Aningeria) altissima, Antiaris toxicaria, Argomuellera macrophylla,
Artabotrys likimensis, Bequaertiodendron oblanceolatum, Blighia unijugata, Celtis
gomphophylla, C. mildbraedii, Clerodendrom buchholzii, C. johnstoni, Coffea
eugenioides,
Craterispermum
schweinfurthii,
Culcasia
falcifolia,
Dracaena
fragrans, D. laxissima, Entandophragma angolense, Ficus asperifolia, F.
exasperate,
F.
vallis-choudae,
Funtumia
africana,
Gouania
longispicata,
Harungana madagascariensis, Hippocratea africana, Jasminum fluminense,
Landolphia buchananii, Maesopsis eminii, Monodora whitei, Premna angolensis,
Pseuderanthenum
ludovicianum,
Rothmannia
longiflora,
Trichilia
emetica,
Uvariopsis congensis and Venronia conferta.
The Afromontane species include Albizia gummifera, Allophylus abyssinicus,
Apodytes
dimidiata,
Cassipourea
ruwensorensis,
Chaetacme
aristata,
100
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Chyrsophyllum albidum, C. viridifolium, Croton macrostachyus, C. megalocarpus,
Deinbollia
kilimandscharica,
Diospyros
abyssinica,
Ekebergia
capensis,
Lepidotrichilia volkensii, Macaranga kilimandscharica, Neoboutonia macrocalyx,
Nuxia congesta, Olea capensis, Oncoba spinosa, Oxyanthus speciosus, Polyscias
fulva,
Prunus africana, Rapanea melanophloeos, Ritchiea albersii, Stombosia
scheffleri, Syzigium guineense, Teclea nobilis, Trichocladus ellipticus, Urera
hypselodendron, and Vangueria apiculata.
The transitional species include Alangium chinense, Alchornea laxiflora, Bridelia
micrantha, Clausena anisata, Clematis brachiata, Croton sylvaticus, Dalbergia
lactea, Dombeya burgessiae, Dovyalis macrocalyx, Ehretia cymosa, Erythrococca
atrovirens, Ficus natalensis, F. sur, F. thonningii, Flacourtia indica, Grewia similes,
Kigelia africana, Maesa lanceolata, Margaritaria discoidea, Maytenus heterophylla,
Morus mesozygia, Pavonia urens, Rawsonia lucida, Rothmannia urcelliformis,
Sapium ellipticum, Stereospermum kunthianum, Strychnos usambarensis, Tinnea
aethopica, Trema orientalis, Trilepisium madagascariense, and Vitex fischeri.
Twenty-seven woody species recorded by Althof (2005) were not recorded in other
parts of Kenya. These include Acacia montigena, Achyrospermum parviflorum,
Pouteria (Aningeria) altissima, Bequaertiodendron oblanceolatum, Cassipourea
ruwensorensis, Chionanthus mildbraedii, Chrysophyllum albidum, Clerodendrum
buchholzii, Craterispermum schweinfurthii, Dracaena fragrans, Entandophragma
angolense, Illigera pentaphylla, Leea guineense, Maesopsis eminii, Monodora
myristica, Oreobambus buchwaldii, Ouratea densiflora, Ouratea hiernii, Piper
guineense, Premna angolensis, Pseuderanthenum ludovicianum, Rothmannia
longiflora, Rothmannia sp., Uncaria africana, Uvariopsis congensis, and Vernonia
conferta. In addition, Althof (2005) recorded the endemic herb Commelina albiflora
and 15 woody species for the first time in Kakamega Forest including Agelaea
pentagyna, Artabotrys likimensis, Basella alba, Connarus longistipitatus, Dregea
abyssinica, Leptaspis cochleata, Meyna tetraphylla, Monanthotaxis buchananii,
Smilax anceps, Suregada procera, and Turraea abyssinica.
Althof (2005) described the plant communities Kakamega Forest based on the
Braun-Blanquet method. In total, thirteen plant communities and subcommunities
belonging to two alliances, i.e., Antiaris toxicaria–Diospyros abyssinica alliance
101
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
representing the mature forest stage and Harungana madagascariensis–
Desmodium adscendens alliance representing the young forest stage, were
identified from the main forest block and fragments.
Plant communities and subcommunities of the Antiaris toxicaria–Diospyros
abyssinica alliance:
1. Trichocladus ellipticus subcommunity is named from the differential species and
is said to represent a climax stage of development in the near-primary Kisere
forest.
2. Ficus cyathistipula subcommunity is characterized by the presence of Ficus
cyathistipula and F. bubu and is localized in Ghostisland part of the Buyangu
National Reserve.
3. Uvariopsis congensis community can be distinguished by the differential
species Uvariopsis congensis and is restricted to the study sites at Kisere,
Buyangu Hill, Colobus and Ghostisland.
4. cf. Fernandoa magnifica community occurs in places at Kisere, Buyangu Hill
and Colobus and is characterized by the differential species cf. Fernandoa
magnifica and Rawsonia lucida and Strychnos usambarensis. Deinbollia
kilimandscharica and Markhamia lutea are the associated species in the shrub
layer.
5. Degraded Rapanea melanophloeos community is found in a disturbed area
along Isiukhu river. It is distinguished by the characteristic species Rapanea
melanophloeos and Nuxia congesta.
6. Pure Deinbollia kilimandscharica – Markhamia lutea community is found in
Buyangu Hill. It is a middle-aged secondary forest community characterized by
Rawsonia lucida, Strychnos usambarensis and Coffea eugenioides.
7. Deinbollia kilimandscharica – Markhamia lutea transitional subcommunity is
found in the Udo camp site and Vihiga area and is characteristic of young forests.
102
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
8. In Suregada procera subcommunity, Suregada procera is the differential
species and the liana Landolphia buchananii is the characteristic species. The
community is found in Yala and Ikuywa forests.
9. Pseuderanthemum ludovicianum subcommunity is found in parts of Salazar,
Busambuli, Isecheno, Yala and Ikuywa and is described as a middle-aged
secondary community.
10. Strombosia scheffleri community is a middle-aged secondary community and
is found in parts of Isecheno forest.
11. In Pure Celtis mildbraedii – Craibia brownii community, Celtis mildbraedii and
Craibia brownii are characteristic species in the tree layer and Bequaertiodendron
oblanceolatum and Chrysophyllum albidum are the characteristic species in the
shrub layer.
Plant community and subcommunity of the Harungana madagascariensis–
Desmodium adscendens alliance:
1. Maesa lanceolata subcommunity is characteristic of a disturbed forest and is
found in the forest around the Udo camp site. The community is characterized by
the abundance of Maesa lanceolata, Acanthus pubescens, and Pavonia urens.
2. Pittosporum viridiflorum community is the youngest of all investigated
succession stages in Kakamega Forest.
5.1.5 Fauna
Kakamega Forest is known for its animal diversity. It is home to five diurnal
primate species: the Black and White Colobus (Colobus guereza), the Red-tailed
Monkey (Cercopithecus ascanius), the Blue Monkey (Cercopithecus mitis), the De
Brazza’s Monkey (Cercopithecus neglectus), and the Olive Baboon (Papio anubis)
(Fashing & Cords 2000). Other large mammals in the forest include the Bushbuck
(Tragelaphus scriptus), the Waterbuck (Kobus ellipsiprymnus), the Bushpig
(Potamochoerus larvatus), the Blue Duiker (Cephalophus monticola), the Red
103
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Duiker (Cephalophus harveyi), and the Common Duiker (Sylvicarpa grimmia)
(Blackett 2004).
The avifauna of Kakamega Forest is quite remarkable with a unique combination
of central African lowland species and highland species, the lowland species being
the dominat. Zimmerman (1972) shows that the avifaunal affinities of Kakamega
Forest relate with the lowland Congo and western Uganda forests, as indicated by
the 107 species they share in common. More than 350 species of birds are found
in Kakamega Forest (KIFCON 1994). Sixty-two birds of Kenya are restricted to
Kakamega Forest including Turner’s Eremomela (Eremomela turneri) and
Chapin’s Flycatcher (Muscicapa lendu) which are globally threatened species
(Sayer et al. 1992).
Kakamega Forest is rich in amphibians and reptiles. Many of the snakes in
Kakamega Forest are from West Africa including the Forest Cobra (Pseudonaje
goldii),
the
Black-lipped
Cobra
(Naja
melanoleuca),
Jameson's
Mamba
(Dendroaspis jamesoni), the Bush Viper (Atheris squamigera), the Rhinoceroshorned Viper (Bitis nasicornis) and the Gaboon Viper (Bitis gabonica). Veith
(2004) recorded 28 species of frogs from Kakamega forest.
Insects, especially butterflies (Lepidoptera) are diverse in Kakamega Forest with a
total of 515 species, representing 60% of the total butterfly species in Kenya
(Häuser 2004). In addition, 71 species of dragonflies (Clausnitzer 2004) and more
than 190 species of bees (Kraemer & Naumann 2004) have been recorded from
the forest.
5.1.6. Management Status
Historical records (Mitchell 2004) indicate that the first forest boundary of
Kakamega was physically established around 1908-1910. This boundary was later
modified in1912-13 and in 1929-1932. During these periods, the forest used to be
managed by the local people and village elders until its management was taken
over by the Forest Department in 1931 (Mitchell 2004). In 1933, Kakamega Forest
was first gazetted as a Trust Forest under Proclamation No. 14
and it was
declared as a Central Forest in 1964 (Blackett 1994). In 1967, the Isecheno,
Kisere and Yala Nature Reserves were established and gazetted. In 1986, the
104
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
northern part of Kakamega Forest (Buyangu area) and Kisere forest were gazetted
as Kakamega National Reserve and fell under management of the Kakamega
Wildlife Reserve (KWS) which is a quasi-government body operating under the
Ministry of Environment and Natural Resources. The southern part of the main
forest block (Isecheno), and the fragments Malava, Yala, Ikuywa, and Kaimosi are
managed by the Forest Department (FD) under the Ministry of Environment and
Natural Resources.
The aim of the KWS is to conserve, protect and sustainably manage wildlife
resources (Wass 1995). The areas under KWS managements are kept for
conservation and tourism only and people are not allowed to collect any forest
products. The aim of the FD is to enhance conservation and protection of
indigenous forest, to improve the production of timber and fuelwood and to
establish a framework for the long-term development forestry (Wass 1995). Cattle
grazing, collection of dead firewood, medicinal plants and thatching grass are
permitted in FD controlled area, while logging and charcoal burning is illegal
(Glenday 2006).
5.1.7. Human Impact
Kakamega Forest is found in an area with one of the highest human population
densities in Kenya (Tsingalia 1990) with an average of 600 people per square
kilometer (Blackett 1994). Human settlement inside the forest was widespread
until its gazettement. This high population density has led to considerable longterm human influence on the forest (Wass 1995). The local people have long used
the forest for shamba system farming, as a thoroughfare for herding cattle to
grasslands in the forest interior and as a source of charcoal, fuelwood, gold,
honey, medicinal plants, timber, and construction materials and hunting of wild
animals (Kokwaro 1988, Wass 1995, Mitchell 2004). The area surrounding the
forest is used for growing maize, tea and sugar cane. Illegal logging, charcoal
burning and grazing by domestic animals is prevalent in the forest (see Figs. 5.5 to
Fig. 5.8). Bleher et al. (2005) conducted an assessment of human impact in
Kakamega Forest and showed a high level of human impact throughout the forest
with illegal logging and extraction of commercially valuable timber being most
widespread.
105
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Fig. 5.5 Cattle grazing in Kaimosi forest
Fig. 5.6. Charcoal making place in Ikuywa forest
106
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Fig. 5.7. Firewood collection in Ikuywa forest
Fig. 5.8. Tee plantation adjacent to Isecheno forest
107
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
5.1.7.1 Fragmentation
Kakamega Forest is a highly fragmented and disturbed forest (Tsingalia 1990,
Bleher et al. 2006) and what is known as Kakamega Forest at present consists of
the main forest block with an area of 8,537 ha, surrounded by five forest fragments
(Kisere, Malava, Yala, Ikuywa & Kaimosi) with area of 132 to 1,370 ha (Farwig et
al. 2007).
To what extent the Kakamega Forest was extending and contiguous to the various
fragments is debatable. Brooks et al. (1999) argued that at the time of British
colonization of Kenya in 1895, Kakamega Forest was contiguous with what are
now the peripheral fragments of Yala, Ikuywa, Kisere, and Malava, and eastwards
up the Nandi Escarpment to the Nandi forest above 1800 m. According to these
authors, Malava forest was isolated from Kakamega Forest between 1895 and
1917, Kisere forest was isolated around 1933, Yala forest was isolated at the
beginning of 1970, and Ikuywa forest was isolated in 1976.
Mitchell (2004), who conducted a detail analysis on the fragmentation and
disturbance history of Kakamega Forest, argued that Kakamega Forest was
contiguous only with the forests of Yala and Ikuywa in the southern part and the
forests of Malava, Kisere and North Nandi have always been separate from
Kakamega Forest. The fragments Yala and Ikuywa have been separated from the
main forest block since the early 1960s and Kaimosi was separated between 1913
and 1959 (Mitchell 2004).
5.1.7.2 Logging
Commercial logging in Kakamega Forest started after the gold rush of the 1930’s
and its pit prop and fuel wood requirements (Mitchell 2004). Licenses for timber
extraction were given to sawmills in 1933 and since then the forest was logged by
clear-felling and selective logging. Clear-felling of indigenous forest to make way
for fast-growing exotic tree and softwood plantations as well as for settlement and
tea plantation was extensive under colonial forest service (Bleher et al. 2006).
Clear-felling was officially halted in 1975 but selective logging for a wide range of
species continued till the mid-1980’s when the exploitation of indigenous trees was
banned by presidential decree (Mitchell 2004).
108
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
5.1.7.3 Plantation
Plantation of indigenous trees in Kakamega Forest started south of Isecheno
around 1934 (Mitchell 2004). The trees planted include Prunus africana, Olea
capensis, Markhamia lutea, Croton megalocarpus, Spathodea campanulata,
Zanthoxylum gillettii, Cordia africana, Funtumia africana and Maesopsis eminii.
Since the late 1940s, vast area of Kakamega Forest has been converted to
forestry plantations including coniferous trees of Pinus patula, P. caribaea, and
Cupressus lusitanica (Tattersfield et al. 2001). Blackett (1994) estimated 1,700 ha
of plantations concentrated around Isecheno forest station whereas Mitchell
(2004) estimated 1,700 to 2,400 ha of plantations in Kakamega Forest.
5.1.7.4 Change in land cover and forest area
As a result of the continuous human pressure in the previous century, Kakamega
Forest has undergone a change in land cover resulting in a reduction of the
indigenous forest cover. In addition, the observed difference in the floristic
composition and structure within Kakamega Forest is partly attributed to the
exploitation history of the forest (Kiama & Kiyiapi 2001, Althof 2005).
An assessment of land cover development trends since the early 1970’s (Glenday
2006, Lung & Schaab 2006) has revealed severe forest loss in the north-western
and the southern parts of Kakamega Forest and succession in the north-eastern
and north-central parts of the forest. Lung & Schaab (2006) reported a reduction
of the near-natural and old secondary forests from 15,000 ha in 1972 to 12,200 ha
in 2001, and an increase in bushland from 1,000 ha to 4,000 ha. Table 5.1
presents changes in areas of Kakamega main forest block and fragments for a
period of 70 years since the forest was gazetted in 1933. Malava forest showed
the highest forest loss with 73% of its forest area being lost in 70 years time.
Kisere forest, on the other hand, had lost only 8.4% of its forest area. The main
forest block, which also included Ikuywa and Yala forest during the time of forest
gazettment, has lost 53% of its forest area.
109
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Table 5.1 Area of Kakamega main forest block and fragments in 1933 and 2001
(Source: BIOTA East- Phase I Final Report)
Main forest block/fragment
Area (ha) in 1933
Area (ha) in 2001
Malava
703
190
Kisere
458
420
23,632 (including Yala &
8,537
Kakamega main forest block
Ikuywa)
Ikuywa
Included in the main forest
1,370
block
Yala
Included in the main forest
1,199
block
Kaimosi
-
132
5.2 Study sites
Foliicolous lichens were collected from Kakamega main forest block (Colobus,
Buyangu, Bukhaywa, Busambuli, Campsite, Isiukhu, Ghostisland, Salazar, and
Isecheno) and from the surrounding forest fragments in the northern (Kisere and
Malava) and southern (Yala, Ikuywa, and Kaimosi) part of Kakamega (Fig. 5.9).
Table 5.2 presents the management regime, conservation status, forest type,
disturbance history and plant community types of the study sites of Kakamega
Forest.
110
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Fig. 5.9 Study sites of Kakamega forest
111
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Table 5.2 Characterization of the study sites in Kakamega Forest
Plant community
(Althof 2005)
KWS/National
Reserve
Forest type/
Succession
stage
(Althof 2005)
Middle-aged
secondary
Busambuli
KWS/National
Reserve
Middle-aged
secondary
Small stature vegetation. Several gaps in the canopy and very young
secondary forest sites present. Disturbance high.
Buyangu
KWS/National
Reserve
Middle-aged
secondary
Pure Celtis mildbraedii-Craibia
brownii, Pseuderanthemum
ludovicianum
cf. Fernandoa magnifica,
Uvariopsis congensis, Fernandoa
magnifica
Camp site
KWS/National
Reserve
Young
secondary
Deinbollia kilimandscharica Markhamia lutea transitional
The vegetation is about 10 to 20 years old and the tree layer is up to 12 m
high. Over 60 % of the canopy is closed, but only thin crown layers exist.
Disturbance very high.
Colobus
KWS/National
Reserve
Middle-aged
secondary
Uvariopsis congensis, Fernandoa
magnifica
It was with full forest in 1913/16. In the early 1920s part of the forest was
cleared and converted to farmland. From 1943 sawmills cut timber mainly
Olea capensis, Cordia africana, Canthium schimperanum, Trichilia
emetica, Premna angolensis, Celtis africana, Chrysophyllum albidum,
Funtumia africana, Prunus africana, and Zanthoxylum gillettii. Until 1989
there was a decrease in near-natural and secondary forest, but afterwards
secondary forest expanded. Disturbance intermediate.
Ghostisland
KWS/National
Reserve
Old
secondary
Ficus cyathistipula,
congensis
It is a small forest island in the middle of a Psidium guajava and
Harungana madagascariensis – bushland. Disturabnce intermediate.
Ikuywa
FD/Forest
Reserve
Middle-aged
secondary
Pure Celtis mildbraedii-Craibia
brownii, Strombosia scheffleri,
Suregada procera,
Pseuderanthemum ludovicianum
Study site
Management
regime/Protection status
Bukhaywa
Disturbance history/level
(Mitchell 2004, Althof 2005)
The forest is disrupted by several gaps. The heterogenous forest structure
could be a result of selective logging. Disturbance high.
Uvariopsis
Forest growth colonized much of the grassland areas since the early 20th
century. Pitsawing of Olea capensis, Cordia africana, Canthium
schimperanum, Croton megalocarpus, Prunus africana, Funtumia africana
and Croton sylvaticus took place between1969 and mid 1970’s.
Disturbance intermediate.
Commercial logging started in late 1950s and continued in 1970s and
1980s. Main trees logged: Prunus aficana, Cordia africana, Aningeria
altissima, Zanthoxylum gillettii, Fagaropsis angolensis, Olea capensis,
Cordia africana, and Trichilia emetica. Disturbance low.
112
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Table 5. 2. contd.
Study site
Management
regime/Protection status
Forest type/
Succession
stage
(Althof 2005)
Middle-aged
secondary
Plant community
(Althof 2005)
Disturbance history/level
(Mitchell 2004, Althof 2005)
Pure Celtis mildbraedii-Craibia
brownii, Strombosia scheffleri,
Pseuderanthemum ludovicianum
In 1913/16 the forest west of Isecheno was seriously fragmented. In 1930s
the forest was used for gold prospecting and subsequently logging to
supply the gold mines with fuel and pit props. In 1940s part of the forest
was group planted with Olea capensis, Milicia excelsa, Acrocarpus
fraxinifolius, Zanthoxylum gillettii and Khaya anthotheca. Disturbance high.
Disturbed Deinbollia
kilimandscharica-Markhamia lutea
The1913/16 map shows Kaimosi attached to Kakamega and Kapwaren
forest. Between 1913 and 1959 the forest to the south-east gradually
eroded. The 1950s maps show half of the forest deforested. In 1965 the
local people were pitsawing Olea capensis, Trichilia emetica, Zanthoxylum
gillettii, Celtis mildbaredii, and Croton megelocarpus. Disturbance high.
Isecheno
FD/Forest
Reserve
Kaimosi
FD/Forest
Reserve
Heavily
logged
planted
Isiukhu
KWS/National
Reserve
Young
secondary
Degraded Rapanea
melanophloeos–riverine
community
The forest is found along Isiukhu river. The tree layer is about 15 m high
and a dense shrub layer exists. The plant community belongs to the
middle-aged secondary forest, but species characteristic for disturbed and
young stages also occur. Disturbance high.
Kisere
KWS/National
Reserve
Near-primary
Trichocladus ellipticus, Uvariopsis
congensis,
cf. Fernandoa magnifica
Large-scale logging absent, only pitsawing of Olea capensis, Prunus
africana, Funtumia africana, Cordia africana since 1960. Most part of the
forest under near-natural and old secondary forest. Disturbance low.
Malava
FD/Forest
Reserve
Heavily
logged
planted
Disturbed Deinbollia
kilimandscharica-Markhamia lutea
Salazar
KWS/Nature
Reserve
Middle-aged
secondary
Pure Celtis mildbraedii-Craibia
brownii, Pseuderanthemum
ludovicianum.
Yala
FD/Nature
Reserve
Old
secondary
Pure Celtis mildbraedii-Craibia
brownii, Pseuderanthemum
ludovicianum, Suregada procera
Heavy timber exploitation of Olea capensis and Prunus africana since
1940. Between 1945 and 1957 it has been intensively group planted with
Cordia africana, Prunus africana and O. capensis and exotic trees of
Khaya anthotheca and Bischoffia javanica. Disturbance high.
In 1913/16 part of the forest was covered by grassland with scattered
trees. In 1977/78 logging of Croton megalocarpus, Antiaris toxicaria, Celtis
mildbraedii, Funtumia africana, Aningeria altissima, Olea capensis, Prunus
africana, Cordia africana, Celtis mildbraedii, and Canthium schimperanum.
After 1989 secondary forest expanded. Disturbance low.
It became disconnected from indigenous forest on the northern half of its
boundary in 1950s and 1960s. No large-scale logging but pit-sawing of a
few species took place. It has a mature forest profile of a very low stem
density. Disturbance low.
and
and
113
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
5.3 Results
5.3.1 Floristic composition
A total of 146 taxa belonging to 41 genera and 17 families were recorded from
Kakamega Forest. Out of these 137 species were fully identified to the species
level. Eight taxa were identified to the genus level only. One species was further
identified to a subspecies level and three species were further identified to a
variety level. Five species new to science were discovered. For the sake of
simplicity, in the subsequent presentation, all subgeneric taxa (species,
subspecies and variety) will be treated as species. The full species list of
Kakamega Forest is presented in Appendix 13.
Ninety-two per cent of the lichens recorded from Kakamega Forest were typically
foliicolous, 5% were lichenicolous fungi growing on foliicolous lichens, 3%
facultative foliicolous and 1% ubiquitous (Fig. 5.10)
.
Foliicolous
Facultative
Lichenicolous
Ubiquitous
Fig. 5.10 Proportion of typical, facultative, ubiquitous foliicolous lichens and
lichenicolous lichens
In Kakamega Forest, Pilocarpaceae was the dominant family both in terms of the
number of genera (11) and species (30). The family Porinaceae was the second
dominant in terms of the number of species (25) but with only two genera. The
family Gomphillaceae comprised 7 genera and 19 species. The family
114
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Asterothyriaceae was represented by 3 genera and 12 species. The families
Strigulaceae and Coenogoniaceae which have only one genus comprised 14
species and 12 species respectively.
Among the study sites, the highest number of families of foliicolous lichens were
recorded from Kisere (14 families) followed by Buyangu, Isecheno, Isiukhu, and
Salazar with 13 families each. Eleven families were recorded from Bukhayawa,
Busambuli and Kaimosi. From Colobus and Ghostisland 9 families were recorded
and the least family was recorded from Camp site (7 families). Fig. 5.11 shows
the number of families, genera and species recorded in each forest part of
Kakamega.
90
80
70
No. of taxa .
60
50
40
30
Family
Genus
Species
20
10
C
am
G ps
ho
it
st e
isl
an
Ka id
i
Bu mo
kh si
ay
aw
a
C
ol
ob
us
M
al
Bu av
sa a
m
bu
Is
ec li
he
no
Ik
uy
w
Sa a
la
za
r
Ya
la
Ki
se
Bu re
ya
ng
u
Is
iu
kh
u
0
Fig. 5.11 Number of families, genera and species in the study sites of Kakamega
Forest
The highest numbers of genera (30) were recorded from Isiukhu, followed
respectively by Kisere (28 genera), Buyangu (26 genera), Ikuywa (24 genera),
Salazar and Yala (23 genera each), Malava (20 genera), Busambuli (19 genera),
and Bukhayawa and Isecheno (18 genera). The lowest number of genera were
recorded from Colobus (15 genera), Ghostisland (13 genera) and Camp site (11
genera) (Fig. 5.11).
The highest numbers of species were recorded from Isiukhu (78 species),
Buyangu (75 species) and Kisere (74 species). From Yala, Salazar, Ikuywa, and
115
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Busambuli, Isecheno 69, 67, 63, 54, and 54 species were recorded respectively.
Forty-four species were recorded from Bukhayawa, Colobus, and Malava and the
least number of species were recorded from Ghostisland (31 species) and Camp
site (28 species).
Certain families of foliicolous lichens dominated both in the number of genera and
species in the various study sites of Kakamega (see Figs. 5.12 & 5.13). In the
number of species, the family Porinaceae was the most dominant in Bukhayawa,
Buyangu, Colobus, Ghostisland, Isecheno, Salazar, Malava and Kaimosi. The
family Pilocarpaceae was the most dominant in Busambuli, Kisere, Yala and
Ikuywa. In Isiukhu both Porinaceae and Pilocarpaceae were equally dominant. In
the Camp site forest, the family Asterothyriaceae was the most dominant.
The family Strigulaceae was the second dominant in Bukayawa, Busambuli,
Ghostisland, Isecheno and Malava. In Buyangu and Kaimosi the family
Pilocarpaceae was the second dominant. Gomphillaceae was the second
dominant family in the Camp site, Isiukhu, and Ikuywa.
In Colobus
Coenogoniaceae and Strigulaceae were the second dominant while in Salazar
Coenogoniaceae was the second dominant. In Kisere and Yala Porinaceae was
the second dominant.
116
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
A
Verrucariaceae
Thelotremataceae
Strigulaceae
Roccellaceae
Ramalinaceae
Porinaceae
Salazar
Pilocarpaceae
Isiukhu
Isecheno
Monoblastiaceae
Ghostislanid
Microthyriaceae
Colobus
Camp site
Lyrommataceae
Buyangu
Busambuli
Gomphillaceae
Bukhayawa
Coenogoniaceae
Coccocarpiaceae
Bacidiaceae
Asterothyriaceae
Aspidotheliaceae
Arthoniaceae
0
2
4
6
8
10
No. of genera
Verrucariaceae
B
Strigulaceae
Ramalinaceae
Pilocarpaceae
Kaimosi
Ikuywa
Microthyriaceae
Yala
Malava
Gomphillaceae
Kisere
Coccocarpiaceae
Asterothyriaceae
Arthoniaceae
0
2
4
6
8
10
No. of genera
Fig. 5.12 Number of genera per family in the main forests (A) and fragments (B) of
Kakamega
117
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Verrucariaceae
A
Thelotremataceae
Strigulaceae
Roccellaceae
Ramalinaceae
Porinaceae
Salazar
Isiukhu
Pilocarpaceae
Isecheno
Monoblastiaceae
Ghostislanid
Microthyriaceae
Colobus
Camp site
Lyrommataceae
Buyangu
Gomphillaceae
Busambuli
Bukhayawa
Coenogoniaceae
Coccocarpiaceae
Bacidiaceae
Asterothyriaceae
Aspidotheliaceae
Arthoniaceae
0
5
10
15
20
No. of species
B
Verrucariaceae
Strigulaceae
Ramalinaceae
Kaimosi
Pilocarpaceae
Ikuywa
Yala
Microthyriaceae
Malava
Kisere
Gomphillaceae
Coccocarpiaceae
Asterothyriaceae
Arthoniaceae
0
5
10
15
20
No. of species
Fig.5.13 Number of species per family in the main forest parts (A) and fragments
(B) of Kakamega
118
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
The distribution of species in the various forest parts of Kakamega is not uniform.
Many species are restricted to some forest parts and not to others. Only seven
species were common for the 14 forest parts. These species were Calenia
monospora, Gyalectidium filicinum, Porina epiphylla, P. nitidula, P. rubentior,
Trichothelium pauciseptatum and Strigula smaragdula. Seven species recorded
from 13 forest parts were Calopadia fusca, C. puiggarii, Porina cupreola var.
cupreola, P. subpallescens, Strigula phyllogena (all absent from Camp site),
Strigula microspora (absent from Kaimosi), and S. nitidula (absent from
Ghostisland). Coenogonium geralense, Byssoloma leucoblepharum, Strigula
macrocarpa, and Strigula schizospora were recorded from 12 forest parts, all
being absent from Camp site, the first three were absent from Kaimosi and the last
species was absent from Bukhayawa. Six species recorded from 12 study sites
were Calenia aspidota (not recorded from Bukhayawa, Camp site & Malava),
Lyromma nectandrae (not recorded from Busambuli, Camp site, & Malava),
Bacidina apiahica (Isecheno, Isiukhu & Yala), Opegrapha phylloporinae (not
recorded from Camp site, Ghostisland and Salazar), Strigula obducta (not
recorded from Camp site, Ghostisland and Kaimosi) and Chroodiscus verrucosus
(not recorded from Bukhayawa, Colobus and Kaimosi).
Twenty-eight species were recorded from one study site only. Fellhanera parvula,
Arthonia flavoverrucosa, Arthonia fuscocyanea, Musaespora kalbii, Porina lucida
var. lucida (all recorded from Buyangu only). Asterothyrium septemseptatum ssp.
africanum, Asterothyrium sp., and Psorotheciopsis gyalideoides were recorded
from Camp site only. Fellhanera encephalarti, Strigula janeriensis, and
Chroodiscus australiensis were recorded from Ikuywa. Eremothecella calamicola,
Aspidothelium geminiparum, A. scutelicarpum, Aderkomyces dilatatus, Aulaxina
opegraphina, Calenia sp., C. thelotremela, Gyalideopsis cochlearifer, and Porina
atrocoerulea
were
recorded
from
Isiukhu
only.
Arthonia
atropunctata,
Aspidothelium hirustum sp. nov., Byssolecania hymenocarpa and Tapellaria
nigrata were recorded from Kisere only. Lichenopeltella epiphylla and Porina
pallescens were recorded from Salazar. Porina kamerunensis and Bacidia
medialis was recorded from Colobus and Malava respectively. The distribution of
foliicolous lichens in the study sites of Kakamega is presented in Appendix 14.
119
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
5.3.2 Species frequency
The frequency of occurrence of species in the various study sites of Kakamega is
presented in Fig. 5.14. In all study sites except in Isecheno, Ghostisland and
Kaimosi, species classified as rare constituted the highest proportion. The highest
proportion of rare species was recorded from Buyangu (80%). In Isecheno species
classified as occasional constituted the highest proportion (31%) and rare species
constituted 25% of the whole species. In Ghostisland and Kaimosi, species
classified as rare are absent and occasional species have the highest proportion.
Species classified as occasional constituted the second largest proportion in
Busambuli, Bukhayawa, Camp site, Colobus, Isiukhu, Kisere, Malava and Salazar.
Dominant species constituted the second highest proportion only in Bukhayawa.
Porina nitidula is the dominant species in all study sites except in the camp site
forest. Porina epiphylla is the dominant species in Bukhayawa, Busambuli,
Buyangu, Colobus, Isecheno, Isiukhu, Kaimosi, Kisere, Malava, Slazar and Yala.
Except in Busambuli, Camp site, Ghostisland, and Kaimosi, Porina rubentior is the
dominant species in the remaining study sites. Porina cupreola var. cupreola is the
dominant species in Bukhayawa, Ghostisland, Ikuywa, Isiukhu, Kisere, Malava,
Salazar and Yala.
Species which are dominant in only one study site were Asterothyrium rotuliforme
in Camp site, Bacidina apiahica and Coenogonium lisowski in Malava, Calenia
aspidota, Strigula antilarum and S. microspora in Busambuli, and Strigula obducta
and Calopadia puigarii in Bukhayawa. Coenogonium geralense is the only species
which became dominant in two forests, in Bukhayawa and Isecheno. The
frequency occurrences of all species in the study sites of Kakamega are presented
in Appendices 15.
120
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
100%
90%
80%
70%
Rare
60%
Occasional
Less frequent
50%
Frequent
40%
Very frequent
30%
Dominant
20%
Yala
Salazar
Kisere
Kaimosi
Isiukhu
Isecheno
Ikuywa
Ghostislanid
Colobus
Camp site
Buyangu
Busambuli
Bukhayawa
0%
Malava
10%
Fig. 5.14 Proportion (%) of species in the various frequency classes in the study
sites of Kakamega
5.3.3 New and interesting records and new species of foliicolous lichens
In the course of the present study many new species and new records of
foliicolous lichens were discovered. Among the total list of foliicolous lichens and
lichenicolous fungi of this study, 5 species are new to science and 75 species are
new records for Kenya. In addition three specimens belonging to the genera
Asterothyrium, Calenia and Fellhanera seem to be new to science. However,
further collection is needed to verify their identity. The list of new records of
Kakamega Forest is presented in Appendix 13.
121
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
5.3.3.1 Species new to science
1. Aspidothelium hirsutum sp.nov. (Aspidotheliaceae)
This new species is described from Godere Forest. The second record of this
species was collected from Kakamega Forest. See Fig. 3.9 for pictures of the
species
2. Chroodiscus kakamegensis sp.nov. (Thelotremataceae)
Several specimens of this facultative lichenicolous species were collected from
Godere, Budongo and Kakamega forests. For the description of the species see
section 3.3.3.1.
Specimens examined: Malava fragment of Kakamega Forest, 00027’.072’’ N and
034051’542’’, 1630 m, on living leaves of Peddiea fischeri Engl., Strychnos
usambarensis Gilg; 18.8.2006, Kumelachew 433, 434, 436, 438 (KOBL); Kaimosi
fragment of Kakamega Forest, 00007’.743’’ N and 034050’.458’’ E, 1630 m, on
living leaves of Hippocratea sp., 19.8.2006, Kumelachew 447 (KOBL);
Ghostisland, Kakamega Forest, 00021’.057’’ N and 034051’.668’’ E, 1600 m, on
living leaves of Chrysophyllum albidum G. Don., Kumelachew 477 (KOBL);
Isecheno site of Kakamega Forest, 00014’.522 N and 0340 51’.959’’E, 1580 m, on
living leaves of Heinsenia diervilleoides K.Schum. and Dracaena fragrans,
Kumelachew 489 & 491 (KOBL); Kisere fragment of Kakamega Forest,
00023’.151’’ N and 034053’.595’’ E., 1580 m, on living leaves of Diospyros
abyssinica, Kumelachew 541 (KOBL); Salazar, Kakamega Forest, 00019’.935’’ N
and 034052.649’’, 1560 m, on living leaves of Cassipourea ruwensorensis (Engl.),
Kumelachew 578 (KOBL).
3. Enterographa fellhaneroides sp. nov. (Roccellaceae) Fig. 5.15
This new species is closely related to Enterographa perez-higaredae described
from Mexico (Herrera-Campos & Lücking 2002) in having shortly lirelliform
ascomata, excipuloid tissue and hypothecium filled with grayish crystals and
hypothecial socle. They differ in the size of apothecia, number of ascospore septa
and size of ascospores and asci. Morphologically, E. fellhaneroides looks similar
to E. seawardii, a foliicolous species described in Sparrius (2004) from the
122
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Seychelles Islands, because of similar prominent, open, angular-rounded to
shortly lirellate ascomata with pale orange discs.
Fig. 5.15 Enterographa fellhaneroides sp. nov.
Specimens examined: Kakamega Forest, Kisere fragment, 00022’.966 N,
034053’.751 E, 1594 m, on living leaves of Chrysophyllum albidum G.Don., 15. 08.
2006, Kumelachew 373 (KOBL); Kisere fragment, 00023’.151 N, 034053’.595 E,
1580 m, on living leaves of Teclea nobilis Del., Dracaena fragrans and
Cassipourea ruwenzorensis (Engl.) Alston, 24 August 2006, Kumelachew 538,
539 & 537 (KOBL); Kakamega Forest, Isecheno, 00014’.522 N, 034051’.959 E,
1580 m, on living leaves of Cassipourea ruwenzorensis, 21. 08. 2006,
Kumelachew 484 & 493 (KOBL).
4. Enterographa meklitiae sp. nov. (Roccellaceae) Fig. 5.16
This new species of Enterographa is different from the other species of the genus
by the presence of punctiform ascomata arranged in groups in pseudostromata. In
123
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
the genus this type of ascomata is so far recorded from the lichenicolous fungi
Enterographa epiphylla (Ertz et al. 2005).
Fig. 5.16 Enterographa meklitiae sp. nov.
Specimen examined: Kakamega Forest, Isecheno, 00014’.522 N, 034051’.959 E,
1580 m, on living leaves of Cassipourea ruwensorensis, 21 08. 2006, Kumelachew
484 (KOBL).
5. Gyalidea psorothecioides sp. nov. (Asterothyriaceae) Fig. 5.17
This new species is characterized by marginally black apothecia and 1-septate
ascospores. The two foliicolous Gyalidea (Gyalidea epiphylla & G. phyllophila)
hitherto described have apothecial margin concolorous with the disc and
ascospores are 3(4-5)-septate in G. epiphylla and 3-6 septate in G. phyllophila.
The presence of black apothecia margin makes this new species similar to
Psorotheciopsis (Asterothyriaceae) but unlike the later genus, this new species
has no cellular cortex.
124
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Fig. 5.17 Gyalidea psorothecioides
Specimen examined: Kakamega Forest (Colobus, Mukangu trail) 00021’276’’ N
and 034051’519 E, 1609 m, 14.08.2006, on living leaves on Tiliacora funifera
(Miers) Oliv., Kumelachew 350 (KOBL, holotype).
5.3.3.2 Interesting records of foliicolous lichens
In addition to the above five foliicolous lichen species described as new to science,
certain specimens belonging to the genera Asterothyrium, Calenia, Fellhanera,
Strigula were found to be interesting records which require further collection to
identify their taxonomic status.
1. Asterothyrium sp. (Asterothyriaceae) Fig. 5.18
The specimen cited below is an unknown taxon of the genus Asterothyrium having
a green thallus, typical cortex, 1-septate spores. I presume it is new to science, but
the material is scanty to describe it as new species.
125
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
a
b
Fig. 5.18. Asterothyrium sp. a) Thallus with apothecia, b) ascospores in ascus
Specimen examined: Kakamega Forest, camp site, 00021.134 N, 034051.923 E,
1581 m, 20.08.06, Kumelachew 458, (KOBL)
2. Calenia sp. (Gomphillaceae) Fig. 5.19
Thallus is pale green, non dispersed, slightly applanate verrucae, apothecia
medium sized, marginally slightly raised, with triangular lobules towards the
center, disc grayish, slightly pruinose; ascospores 5-9 septate, 30-40 x 8-10 µm, 48 per ascus. The specimen looks like Calenia obtecta or Calenia pernambucensis
to be described by Robert Lücking in Flora Neotropica (Lücking 2008).
a
b
Fig. 5.19 Calenia sp. a) Thallus with apothecia, b) ascospores in ascus
126
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
3. Fellhanera aff. bouteillei (Pilocarpaceae) Fig. 5.20
Fellhanera bouteillei is a ubiquitous species having a bluish white to bluish gray
thallus, apothecia disc pale flesh-coloured to yellowish, margin indistinct and
ascospores 10-15(-18) x 3-5(-6) µm (Santesson 1952). The specimens cited below
are close to Fellhanera bouteillei but with some differences. Thallus green, rather
coherent, apothecia medium sized, pale orange to brownish orange, with a thin but
distinct margin, spores 1-septate, 18-25 x 4-4.5 µm.
Fig. 5.20 Fellhanera aff. bouteillei
Specimens examined: Kakmega forest, Ikuywa, 00012.628 N, 034055.931 E, 1550
m, epiphyllous on Dracaena fragrans and Teclea nobilis, 23.08.06, Kumelachew
190 & 192 (KOBL).
4. Sporopodium sp. (Pilocarpaceae) Fig. 5.21
Three collections from Kisere and Isiukhu forests of Kakamega were close to
Sporopodium leprieurii but the thallus of these specimens are smooth.
127
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Fig. 5.21 Sporopodium sp.
5. Strigula microspora (Strigulaceae) Fig. 5.22
The specimen of Strigula microspora cited below has got microconidia with long
appendages on both ends. Like the typical species, the microconidia are 1septate, bacilliform, 5 x 1.5 µm. Ascospores are 10-12 x 2.5-3 µm. In the
description of Strigula microspora by Lücking (1991), there is no mention of
presence of appendages on conidia.
128
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
a
b
Fig. 5.22 Strigula microspora (a) Thallus with perithecia (b) conidia with
appendages (arrows)
Specimen examined: Kakamega Forest, Kisere, 00023.053 N, 034053.562 E, 1580
m, epiphyllous on Rawsonia lucida, 24.08.06, Kumelachew 547 (KOBL).
129
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
5.3.2 Alpha diversity
5.3.2.1 Mean species number
Species richness per sample of the various forest parts of Kakamega is variable
ranging from a mean of 5.1 species to a mean of 17.4 species. The mean species
number per sample is highest in Ikuywa and lowest in Camp site (Fig. 5.23).
Kruskall-Wallis test of analysis of variance showed the presence of significant
difference among the medians of species number among the various forest parts
(Kruskall-Wallis Chi-square =61.8, P<0.05). To determine which medians were
significantly different from which others, the Kruskal-Wallis multiple comparison
test was performed. The result of this analysis is presented in Table 5.3.
Mean spcies number
30
25
20
15
10
5
Is
ec
he
no
Is
iu
kh
u
Sa
la
za
r
M
al
av
a
Ki
se
re
Ka
im
os
i
C
ol
ob
us
Bu
ya
ng
G
u
ho
st
isl
an
id
C
am
p
si
te
Ya
la
Ik
uy
w
a
Bu
kh
ay
w
a
Bu
sa
m
bu
li
0
Fig. 5.23 The mean species number per study site in Kakamega Forest (values
are mean ± SD).
Except with Ghostisland and Kaimosi, the mean species number of Camp site
forest is significantly different from the mean of the other forest parts. Buyangu is
significantly different from Ikuywa, Bukhayawa, Busambuli, Yala, Isecheno,
Isiukhu, Salazar, Malava, and Kisere. Colobus is significantly different from
Ikuywa,
Bukhayawa,
Busambuli,
Yala,
Isecheno,
Isiukhu,
and
Salazar.
Ghostisland is significantly different from Ikuywa, Yala, Isecheno, Isiukhu, Salazar,
and Malava. Isiukhu, Kaimosi and Kisere are significantly different from Ikuywa.
130
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Table 5.3 Kruskal-Wallis Multiple-Comparison test between medians of species
numbers of the study parts of Kakamega Forest. * significant ( P<0.05), ns= not
*
*
-
Colobus
*
*
ns
*
-
Ghostisland
*
*
ns
ns
ns
-
Ikuywa
ns
ns
*
*
*
*
-
Isecheno
ns
ns
*
*
*
*
ns
-
Isiukhu
ns
ns
*
*
*
*
*
ns
-
Kaimosi
*
*
ns
ns
ns
ns
*
ns
ns
-
Kisere
*
ns
*
*
ns
ns
*
ns
ns
ns
-
Malava
ns
ns
*
*
ns
*
ns
ns
ns
ns
ns
-
Salazar
ns
ns
*
*
*
*
ns
ns
ns
ns
ns
ns
-
Yala
ns
ns
*
*
*
*
ns
ns
ns
ns
ns
ns
ns
Salazar
*
Malava
Campsite
Kisere
-
Kaimosi
*
Isiukhu
*
Isecheno
Buyangu
Ikuywa
-
Colobus
ns
Camp site
Busambuli
Busambuli
Buyangu
Bukhayawa
Ghostisland
significant
5.3.2.2 Species accumulation curve
Species accumulation (rarefaction) curves were plotted for the foliicolous lichens
observed from each study site in Kakamega Forest (Fig. 5.24). The curves show
the mean number of species for each sample accumulated. Since the unit of the xaxis is number of samples, the resulting rarefaction curves are measures of
species density (Gotelli & Colwell 2001). The 95% confidence intervals of the
respective curves allow to test if there is significant difference in species richness
among the study sites (Table 5.4).
Foliicolous lichen species richness is significantly higher in Isiukhu, Kisere,
Buyangu, Yala and Salazar than the remaining study sites. However, Ikuywa is not
131
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
significantly different from Isiukhu and Yala. Species richness is significantly
higher in Ikuywa than in Bukhayawa, Busambuli, Isecheno, Kaimosi, Malava and
Colobus. Similarly, there is significantly higher species richness in Isecheno and
Bukhayawa than in Colobus and Ghostisland. Species richness is also significantly
higher in Kaimosi than in Ghostisland. The foliicolous lichen species richness of
Camp site is significantly lower than all the other study sites.
Table 5.4 Significance of species richness differences at 95% confidence limit. ns
Ghostisland
Ikuywa
Isecheno
Isiukhu
Kaimosi
Kisere
Malava
Salazar
Yala
ns
*
*
*
ns
*
ns
*
*
*
ns
ns
ns
ns
ns
*
ns
*
ns
ns
Salazar
*
*
*
*
*
*
*
*
*
*
Malava
ns
ns
*
ns
ns
ns
ns
ns
ns
ns
Kisere
*
*
*
*
ns
ns
ns
*
ns
ns
Kaimosi
*
*
*
ns
ns
ns
ns
ns
ns
ns
Ikuywa
-
Ghostisland
*
Colobus
ns
*
Isiukhu
Colobus
ns
ns
*
Isecheno
Camp site
Camp site
Buyangu
Buyangu
Busambuli
Busambuli
Bukhayawa
= not significant, * = significant difference in species richness
-
*
*
* ns
*
*
*
*
ns *
*
*
* ns
*
ns
*
*
ns
ns
ns
ns
*
ns
The species accumulation curves could be used to compare the observed species
richness of sites at similar sample size (usually the smallest). Comparison of the
expected species richness of the study sites of Kakamega by the rarefaction curve
after 9 samples (the sample size of Ghostisland and Kaimosi) provided a mean
species richness of 56.3 for Ikuywa, 49.8 for Isiukhu, 49.5 for Yala, 46.8 for
Busambuli, 43.3 for Salazar, 42.3 for Kisere, 41.6 for Bukhayawa, 41 for Kaimosi,
39.7 for Isecheno, 37.5 for Buyangu, 35.7 for Malava, 32.5 for Colobus, 32 for
Ghostisland and 20.7 for Camp site forest.
132
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
90
No. of species .
80
70
Bukhayawa
Busambuli
60
Buyangu
Camp site
50
Colobus
Ghostislanid
40
Ikuywa
Isecheno
30
Isiukhu
Kaimosi
20
Kisere
Malava
Salazar
10
Yala
0
0
5
10
15
20
25
30
35
Number of samples
Fig. 5.24 Species accumulation curve (rarefaction) of the foliicolous lichens in the
study sites of Kakamega.
5.3.2.3 Estimation of species richness
The various non-parametric species richness estimators for incidence data
provided different values for the estimate of the species richness of the study sites
of Kakamega Forest (Table 5.5). In Bukhayawa, Busambuli, Camp site, Colobus,
Ghostisland, Ikuywa, Isecheno, Isiukhu, Kaimosi, Malava, Salazar and Yala, the
second order Jackknife estimator provided the highest estimate of species
richness. In Buyangu and Kisere the ICE and Chao 2 provided the highest
estimate respectively. The Bootstrap estimator provided the lowest estimate of
species richness for Bukhayawa, Busambuli, Buyangu, Camp site, Colobus,
Ghostisland, Ikuywa, Isiukhu, Malava and Yala. In Isecheno both the Bootstrap
and Chao 2 estimators provided the lowest estimation and the Michalis-Menten
Mean provided the lowest estimate of species richness for Kisere and Salazar.
The difference between the highest and lowest richness estimator varied from 11.5
133
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
species (in Isecheno) to 52 species (in Kisere). The highest difference for Kisere is
due to the very high Chao 2 estimate.
Table 5.5 Number of samples, number of individuals and species richness (with
standard deviation for some) estimate values for the study sites of
Jack 1
Jack 2
Bootstrap
ICE
Degree of
62.1±9.6
61.9±4.4
68.5
54.5
63.8
70 –88
Busambuli
13
173
54
71.1
81.6
73.4±6.2
85
62.3
75.4
64 –87
30
249
75
100.2
136.6
113.7
139.3
91.4
148.7
50 –82
±27.1
±12.4
Camp site
18
92
28
36.7
52±20.2
39.3±3.6
47.5
32.8
43.9
54 –85
Colobus
21
177
45
56
59.1±9.6
59.3±4.6
66
51.7
60.2
68- 87
Ghostisland
9
65
32
55.5
49.8±12
46.2±5.9
55.3
38.3
50
58-84
Ikuywa
14
243
63
78.3
71.9±6.2
76.9±4.6
81.9
69.8
72.3
77-90
Iaecheno
17
214
48
57.2
53.7±4.5
59.3±3
61.6
53.7
57
78-89
Isiukhu
27
339
79
95.2
107±13.7
106.9±4
120.4
91.7
113
70 –86
Kaimosi
9
79
41
77.2
48.1±4.8
56.1±5.6
58.4
48.7
55.9
53 -85.2
Kisere
55
613
77
81.5
181.2
101.6
122.8
86.9
101.4
43-95
±73.9
±6.1
54.1
52.1±6.1
54.5±2.6
59.3
49.6
51.3
76-91
75.3
91.2
88.5±5.1
99.1
77.7
87.7
70-92
91.1±5.6
103.4
79.4
89.2
68-88
(%)
Chao 2
56
collection
MMMeans
48
individuals
204
No. of
14
samples
Bukhayawa
No. of
Sobs
Kakamega
±16.4
Buyangu
Malava
21
246
45
Salazar
37
461
69
±13.3
Yala
25
332
70
82.3
96.9
±15.5
5.3.2.4 Shannon-Wiener diversity
The Shannon-Wiener diversity and evenness values for the study sites of
Kakamega Forest is presented in Table 5.6. Analysis of variance (ANOVA) of the
Shannon diversity index values of the study sites confirmed the presence of
significant differences (F=2.91, p<0.001). Fischer’s least significant difference post
hoc test (Table 5.7) showed that Shannon diversity of Camp site (H’=2.97) is not
significantly different from Colobus (H’=3.42), Ghostisland (H’=3.29) and Malava
(H’=3.42) but significantly lower than the Shannon diversity of the other forest
134
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
parts. The highest value of Shannon diversity is computed for Isiukhu but it was
not significantly different from Bukhayawa, Busambuli, Buyangu, Ikuywa,
Isecheno, Kaimosi, Kisere, Salazar, and Yala. Shannon diversity of Colobus is
significantly lower than those of Ikuywa, Isiukhu, Kisere and Yala. Similarly
Shannon diversity of Ghostisland is significantly lower than those of Ikuywa,
Isiukhu, and Yala. Shannon diversity of Malava is also significantly lower than the
diversity of Ikuywa, Isiukhu, Kisere and Yala.
Table 5.6 Shannon diversity (H’) and evenness (J’) values of the study sites
Shannon index
Shannon evenness index
(H’)
(J’)
Bukhayawa
3.53
0.91
Busambuli
3.69
0.93
Buyangu
3.71
0.86
Camp site
2.97
0.89
Colobus
3.42
0.89
Ghostisland
3.29
0.94
Ikuywa
3.93
0.95
Isecheno
3.52
0.91
Isiukhu
3.92
0.89
Kaimosi
3.57
0.96
Kisere
3.8
0.88
Malava
3.42
0.89
Salazar
3.73
0.88
Yala
3.87
0.91
135
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Table 5.7 Fischer’s least significant difference (LSD) multiple comparison of
Shannon diversity index values among the study sites. ns= not significant, * =
*
*
-
Colobus
ns
ns
ns
ns
-
Ghostisland
ns
ns
ns
ns
ns
-
Ikuywa
ns
ns
ns
*
*
*
-
Isecheno
ns
ns
ns
*
ns
ns
ns
-
Isiukhu
ns
ns
ns
*
*
*
ns
ns
-
Kaimosi
ns
ns
ns
*
ns
ns
ns
ns
ns
-
Kisere
ns
ns
ns
*
*
ns
ns
ns
ns
ns
-
Malava
ns
ns
ns
ns
ns
ns
*
ns
*
ns
*
-
Salazar
ns
ns
ns
*
ns
ns
ns
ns
ns
ns
ns
ns
-
Yala
ns
ns
ns
*
*
*
ns
ns
ns
ns
ns
*
ns
Salazar
*
Malava
Camp site
Kisere
-
Kaimosi
ns
Isiukhu
ns
Isecheno
Buyangu
Ikuywa
-
Colobus
ns
Camp site
Busambuli
Busambuli
Buyangu
Bukhayawa
Ghostisland
significant (p<0.001)
5.3.3 β-diversity and similarity in species composition
Total β-diversity measured by Whittaker’s index of β-diversity (βw) for the study
sites of Kakamega is presented in Table 5.8.
This index of β-diversity is a
measure the degree of turnover or species changes. The highest species turnover
is seen in Buyangu (β-diversity=9). The next highest species turnover is found in
Kisere (β-diversity = 6.9) and Isiukhu (β-diversity = 6.3) respectively. The lowest
turnover is registered in Bukhayawa (β-diversity = 3.3).
136
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Table 5.8 Total β-diversity values along the study sites of Kakamega
Number of
species
(a)
Mean species
number per sample
(b)
β-diversity
(a/b)
Buyangu
75
8.3
9.0
Kisere
77
11.2
6.9
Isiukhu
79
12.6
6.3
Salazar
69
12.4
5.6
Camp site
28
5.1
5.5
Yala
70
13.3
5.3
Colobus
45
8.5
5.3
Kaimosi
41
8.8
4.7
Ghostisland
32
7.2
4.4
Busambuli
54
13.3
4.1
Isecheno
48
12.6
3.8
Malava
45
11.7
3.8
Ikuywa
63
17.4
3.6
Bukhayawa
48
14.6
3.3
Analysis of β-diversity among the study sites based on Sørensen index of
similarity is presented in Table 5.9. The values of the Sørensen index varied from
0.27 to 0.81 indicating variation in β-diversity among the study sites. High
similarity, and thus low β-diversity, is observed between forests of different
succession stages like the middle-aged secondary and the old secondary forest
sites e.g. Salazar and Yala (Ss=0.81) and Ikuywa and Yala (Ss=0.78); the nearprimary forest of Kisere and the old secondary forest of Yala (Ss=0.69). High
similarity (low β-diversity) is also observed between forests of similar development
stages, e.g. between the middle-aged secondary forests of Salazar and Buyangu
(Ss=0.72) and Salazar and Ikuywa (Ss=0.7). Low β-diversity could also be seen
between the young secondary forest of Isiukhu and middle-aged secondary forest
of Buyangu (Ss=0.69). The lowest similarity in species composition, and thus high
β-diversity is observed between the young secondary Camp site forest and the
middle-aged secondary forest of Salazar (Ss=0.27) as well as between the young
137
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
secondary forests of Camp site and Isiukhu (Ss=0.28). In general, the Camp site
forest shows the least similarity with all other forest sites.
0.37
0.46
0.37
-
Colobus
0.69
0.59
0.53
0.30
-
Ghostisland
0.53
0.51
0.54
0.50
0.62
-
Ikuywa
0.58
0.63
0.65
0.40
0.63
0.55
-
Isecheno
0.63
0.53
0.55
0.29
0.66
0.63
0.63
-
Isiukhu
0.54
0.59
0.69
0.28
0.55
0.40
0.62
0.55
-
Kaimosi
0.47
0.57
0.52
0.38
0.56
0.58
0.58
0.58
0.43
-
Kisere
0.62
0.6
0.62
0.32
0.66
0.51
0.66
0.67
0.60
0.53
-
Malava
0.67
0.65
0.53
0.49
0.62
0.65
0.59
0.65
0.45
0.56
0.62
-
Salazar
0.56
0.54
0.72
0.27
0.6
0.53
0.7
0.68
0.61
0.56
0.67
0.53
-
Yala
0.54
0.58
0.65
0.29
0.57
0.49
0.78
0.66
0.64
0.52
0.69
0.52
0.81
Malava
Salazar
Camp site
Kisere
-
Kaimosi
0.56
Isiukhu
0.55
Isecheno
Buyangu
Ikuywa
-
Colobus
0.61
Camp site
Busambuli
Busambuli
Buyangu
Bukhayawa
Ghostisland
Table 5.9 Values of Sørensen index of similarity among the study sites
5.3.4 Ordination
The PCA ordination of the forest sites of Kakamega Forest is presented in Fig.
5.25. The first four axes of PCA explain 51.6% of the total variation in species
composition. The first two axes explain 32.4% of the total variation. The first axis
alone contributes to 18.9% of the total variation. Therefore, the highest variation is
explained by the first PCA axis.
138
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
In the ordination diagram, forest sites that are close to each other are more related
in species composition. Forest sites with high species diversity are positively
correlated with the first PCA axis and sites with low diversity are negatively
correlated with this axis. Forest sites with high disturbance are positively
correlated with the second PCA axis and sites with low disturbance are negatively
correlated with this axis. The ordination diagram shows that the Camp site and
Isiukhu forest sites are different from the other forest sites and explain much of the
variation in the data set. Like Yala, Salazar, Ikuywa, Kisere and Buyangu forest
sites, Isiukhu has high species diversity and is positively correlated with the first
PCA axis. Like the Camp site forest site, it is a disturbed forest and is positively
1.0
correlated with the second PCA axis.
Isiukhu
Camp site
Axis 2
Buyangu
Busambuli
Ghostisland
Malava
Bukhaywa
Kaimosi
Colobus
Isecheno
Ikuywa
-0.6
Kisere
-1.0
Axis 1
Yala
Salazar
1.0
Fig. 5.25 PCA ordination of the study sites of Kakamega Forest.
139
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
5.4 Discussion
5.4.1 Sufficiency of sample size
Complete enumeration of all species of a given community is difficult for many
organisms. Therefore, the most important question in sampling is the sufficiency of
sample size. This is evaluated in this study with the help of a species accumulation
curve and comparison with the species richness estimated by the various nonparametric richness estimators. Except for the species accumulation curves for
Buyangu and Isiukhu which are rising as more samples are pooled, the curves for
the other forests are leveling off and the rate of species accumulation as samples
are successively pooled is highly reducing.
One of the reasons for estimating species richness is to know how much of the
species richness estimated were observed in the sampling, i.e. how much is the
degree of collection of a site. Accordingly, on average 64 up to 88% of the
foliicolous lichens estimated by the various richness estimators have been
collected from the study sites of Kakamega. Heck et al. (1975) reported that
collection of 50% to 75% of the total number of species known to occur in a given
area is satisfactory. In Kisere only 42.5% of the maximum estimated species
richness was collected. However 94.5% of the minimum estimates species
richness was collected.
5.4.2 Alpha-diversity
Lücking and Kalb (2002) reported 92 species of foliicolous lichens and 5 species
of lichenicolous fungi from Kenya. In the present study, 53 of the species already
reported have been encountered in Kakamega Forest. In addition, 77 new records
of foliicolous lichens including 3 lichenicolous fungi and 5 species new to science
are reported from this study, raising the number of foliicolous lichens of Kenya to
171 and the number of lichenicolous fungi to 8. As far as my knowledge is
concerned, this is the highest number of foliicolous lichens so far recorded for a
single country in tropical Africa. Reported numbers of foliicolous lichens include
161 species from Ivory Coast, 124 species from Guinea, 124 species from DR
Congo (Santesson & Lücking 1999) and 144 species from Tanzania (Pócs 1978,
140
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
Farkas 1987, Farkas & Vězda 1987, Farkas 1991, Farkas & Vězda 1993, Feuerer
2007)
High family, generic and species diversity was mostly observed in the forests with
low level of disturbances in both the near-primary (Kisere), old aged secondary
forest site (Yala) and middle-aged secondary forest sites (Ikuywa, Salazar and
Buyangu). In addition high diversity was also recorded in the disturbed forest site
of Isiukhu. Low diversity, on the other hand, was observed in the old secondary
forest of Ghostisland, the middle-aged secondary forest of Colobus, the logged
and planted forests of Kaimosi and Malava and the disturbed young secondary
forest of Camp site. Forest sites where high species diversity were recorded have
relatively closed canopy (e.g. Yala, Buyangu, Kisere) and forest sites with lower
diversity have open or semi-open canopy (e.g. Malava, Kaimosi). The high
diversity at Isiukhu is due to the existence of both semi-open and closed canopy
forests.
The observed species number of a community is mostly biased (Brose et al. 2003)
and excludes rare species, underestimating the true species richness (Palmer
1990, Baltanás 1992).
Species accumulation curves and non-parametric
estimators reduce this bias (Soberón &Llorente 1993, Colwell & Coddington 1994).
The estimation of the expected species richness of the study sites by rarefying all
study sites down to the smallest sample size indicated high species richness in
forests of different seral and/or disturbance stages. High species richness was
respectively estimated for Ikuywa, Isiukhu, and Yala (Fig. 5.24). Low richness was
respectively estimated for Colobus, Ghostisland and Camp site. In general, the
species accumulation curves estimated high foliicolous lichen species richness for
forest sites with low level of disturbance and low species richness for forest sites
with high level of disturbance. Isiukhu is the only forest with high level of
disturbance but with high expected species richness.
Various studies (Sérusiaux 1989, Lücking 1992b, Aptroot 1997, Lücking 1998b)
have reported high foliicolous lichen diversity in undisturbed primary forests and
low diversity in disturbed and secondary forests. In the present study high
foliicolous lichen species diversity was recorded both in a near-primary, slightly
141
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
disturbed forest site of Kisere; old secondary, slightly disturbed forest site of Yala;
middle-aged secondary, slightly disturbed forest sites of
Salazar and Ikuywa;
middle-aged, intermediately disturbed site of Buyangu and a highly disturbed
young secondary forest site of Isiukhu. Although Isiukhu is a disturbed forest, there
are parts with closed forest creating shady understorey and light gap microsite
conditions. In addition, the riverine atmosphere and the relatively high humidity
inside the forest provide suitable microclimatic conditions for many foliicolous
lichens. As a result characteristic foliicolous lichens of the various light regimes are
well represented in Isiukhu making this forest type one of the highest in foliicolous
lichen diversity in Kakamega. In the Buyangu study site forests with closed canopy
and semi-open canopy have been observed. As a result of diversity of microsites
in this forest, the species diversity is also high. Low species diversity was
observed in forest sites with relatively high disturbance (Camp site, Malava,
Kaimosi) and in Ghostisland. Although Ghostisland is said to be an old secondary
forest with little disturbance (Althof 2005), signs of human disturbance and canopy
openings were seen in several places.
The results from this study show that the effect of disturbance on foliicolous lichen
diversity is dependent on the type, frequency and intensity of disturbance (Petraitis
et al. 1989). The diversity of foliicolous lichens is dependent on the availability of
different microsite conditions (Lücking 1997d). If disturbance maintains or
enhances the whole microsite gradient of a forest (e.g. Isiukhu) then there would
be high foliicolous lichen diversity. Contrarily, if disturbance results severe change
in microclimatic conditions and loss of microsites (e.g. Camp site) then diversity of
foliicolous lichens would be reduced. Due to an open canopy in the Camp site
forest, the intensity of light reaching the understorey is high and this reduces the
humidity inside the forest. Althof (2005) recorded the lowest humidity (21.7%) in
this forest type. The most affected by the increased light intensity and reduced
atmospheric humidity are shady understorey species. Many of the foliicolous
lichens recorded from the understorey of Camp site forest are canopy specialists
which have made use of the increased light condition. In Kaimosi, Bukhayawa,
Busambuli, and Malava because of high disturbance, the forest canopy is open in
many places affecting shady understorey species. In these forests light gap
species constituted the highest proportion.
142
Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
5.4.3 Non-parametric species richness estimators
The speed with which the species accumulation curve of an estimator reaches an
asymptote as sample sizes increases indicates the usefulness of an estimator
(Colwell & Coddington 1995). The Michaelis-Menten Means is the only estimator
that appeared to reach an asymptote (curves not shown). The curves of Jack 1
and Bootstrap estimators, though not clearly approaching an asymptote, are
leveling off and predicted comparable species number to the MMMeans. The
Chao 2 and ICE estimators did not seem to be a good estimator as they estimated
high species richness when fewer samples were pooled and the curves did not
stabilize. The curve for the second order Jackknife estimator is rising as more
samples were accumulated. Except the Bootstrap estimator, all the other
estimators of Buyangu predicted high species richness than the observed species.
This is due to the high number of uniques (species restricted to one sample only)
which constituted 53% of the whole species.
The variation in the number of species estimated by the species richness
estimators is due to the dependence of the non parametric estimators on rare
species (uniques and doubletons). In Kisere, for example, based on 77 observed
species, the estimators estimated as low as 82 species and as high as 181
species. Based on the highest estimate 2.4 times more species is expected from
this forest site, which is an unreliable estimate. This is due to the high number of
uniques which accounted for 32.5% of the whole species. Therefore, for the
comparison of species richness of forest sites the rarefaction method is more
reliable than the species richness estimators.
5.4.4 β-diversity
Total β-diversity, computed by dividing the observed number of species of a study
site by the mean number of species, is generally low suggesting low species
turnover in the study sites of Kakamega. A relatively high turnover could only be
seen for Buyangu (β-diversity = 9.0).
There is a wide variation in the values of Søresnson’s index (Ss =0.27-0.81),
indicating variation in species composition (β-diversity). The lowest species
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Diversity of Foliicolous Lichens in Kakamega Forest, Kenya
similarity and thus highest β-diversity is to be observed between Camp site forests
and the remaining forests. Since the camp site forest is very disturbed having
open canopy, many species which are restricted to canopy of closed forests have
grown in the understorey. Furthermore, shady understorey species which are
abundant in the other forest types are scarcely represented in the understorey.
Foliicolous lichen similarity is high between forests of different seral stages (e.g.
Yala vs. Salazar, Yala vs. Ikuywa, Buyangu vs. Isiukhu) as well as between forests
of similar seral stages (e.g. Buyangu vs. Salazar, Salazar vs. Ikuywa). These
results showed no uniform pattern of change in species composition along
succession gradient.
5.5 Conclusion
Kakamega Forest, as the only Guineo-Congolian transitional rainforest in Kenya,
is naturally expected to be the best habitat for foliicolous lichens. Due to various
levels of disturbance and fragmentation, the vegetation of Kakamega Forest
consists of a mosaic of forests of different seral stages, anthropogenic vegetation,
and grasslands, with differing impact on the diversity of organisms. From the result
of this study it can be concluded that:
•
The overall diversity of foliicolous lichens in Kakamega Forest is
considerably high.
•
Differences in diversity of foliicolous lichens among the various forest types
have been shown to depend on the level of disturbance rather than on the
seral stage of forest development.
•
Forest sites with similar seral stages have been shown to differ in their
foliicolous lichen diversity (e.g. Yala vs. Ghostisland, Isiukhu vs. Camp site,
Colobus vs. Ikuywa).
•
Forest sites with closed canopy have high diversity and sites with semiopen and open canopy have low diversity. Canopy openness in Kakamega
Forest is related to the level of disturbance.
•
Foliicolous lichen diversity has been found to be high in the forest sites of
Yala, Isiukhu, Kisere, Salazar, Buyangu and Ikuywa.
144
A Comparative Analysis of Godere, Budongo and Kakamega Forests
Chapter 6. DIVERSITY OF FOLIICOLOUS LICHENS
ALONG DISTURBANCE GRADIENT: A
COMPARATIVE ANALYSIS OF GODERE,
BUDONGO AND KAKAMEGA FORESTS
6.1 Introduction
Due to over exploitation by the local people, and state and private enterprises, the
natural forests of Ethiopia, Uganda and Kenya have declined both in size and
quality. The most serious threats to the natural forests come from forest clearance
due to an increasing human population which require new land for agriculture and
settlement, and from forest degradation due to timber logging and other
unsustainable exploitative activities. As a result, most of the natural forests in
these countries are secondary with different level of disturbances.
Forest destruction and degradation has an obvious, deleterious effect on
biodiversity and environment. If the present trends of deforestation continue, then
many plant and animal species could locally be extinct. Since tropical biodiversity
is not fully explored, many undiscovered taxa could have been or will be lost even
before we discover and name them. The situation is more serious for some
organisms whose diversity and distribution are not known. In order to curb some of
these problems, natural forest should be conserved and managed. Under the
present trend of human population growth and socio-economic situations which
have resulted in intense competition for land for subsistence and commercial
agriculture as well as for industrial development, protection of the whole natural
forests of an area is not feasible. However, some areas could be selected and
designated as conservation sites. Biodiversity is one of the useful parameter used
for the selection of sites for the purpose of conservation (Goldsmith 1987).
Biodiversity includes species diversity, genetic diversity and ecosystem diversity.
Species diversity is the most obvious and frequently used measure of biodiversity.
Species diversity in tropical forests, however, is not fully understood and this
necessitates their immediate documentation.
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
The vascular plant floras of Ethiopia, Uganda and Kenya are relatively well known
due to the publications of the Flora of Tropical East Africa and Flora of Ethiopia
and Eritrea. Documentation of the cryptogamic flora of these countries is at its
infancy stage. Lichens in general and foliicolous lichens in particular are among
the least studied (or unstudied) organisms in these countries as well as in tropical
Africa.
In order to include foliicolous lichens in the forest conservation program and to use
them, as component of biodiversity, in the selection of forest sites for the purpose
of conservation, their diversity and distribution should be documented. Since the
monographic work of Santesson (1952), there has been an increasing attention on
the systematics of foliicolous lichens. However, very little is known about their
ecology and the impact of forest disturbance on their diversity, especially in the
forests of tropical Africa. In this study, comparison of the diversity of foliicolous
lichens along disturbance gradient from Budongo (comparatively least disturbed)
to Kakamega (comparatively medium disturbance) and Godere (comparatively
more disturbed) is presented with the following objectives.
•
To describe the species composition of the foliicolous lichens of the three
forests
•
To compare the α- and β-diversity of foliicolous lichens of the three forests
•
To compare the similarity in foliicolous lichen species composition of the
three forests
•
To analyse the foliicolous lichen species diversity along disturbance
gradient
•
To identify foliicolous lichen species that could be used as bioindicator of
forest types
•
To analyse the biographical distribution of the foliicolous lichens of the
study area.
6.2 Study area
A detailed description of Godere, Budongo and Kakamega forests are presented
in Chapters 3, 4 and 5. The three forests selected for the study of the diversity of
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
foliicolous lichens share several topographic, and physiognomic and climatic
characters (Table 6.1). They are situated on flat terrains with gentle slope, at
medium altitudes and in similar climatic conditions. Godere and Kakamega forests
are composed of a mixture of afromontane and Guineo-Congolian floral elements
as well as transitional species. Budongo Forest is a Guineo-Congolian rainforest.
Most of the canopy species in both forests are deciduous. Climatically, the three
forests are located in high rainfall areas of the respective countries.
Due to the different socio-economic conditions where the three forests are found,
the management regime, degree of anthropogenic disturbance and the land use
are substantially different. Forest management in Budongo and Kakamega is
much better than in Godere where no forest management plan is in place. Due to
different management and exploitation history, the three forests are now found in a
different disturbance conditions.
Among the three forests, Budongo is the least disturbed with undisturbed primary
and disturbed secondary forests located in close proximity. Timber has been
selectively extracted from the forest since 1910. In 1957 clear-cutting was
promoted and enrichment planting of mahoganies (Khaya and Entandrophragma)
and Maesopsis was established in plantations (Paterson 1991). In addition,
arboricide treatment was applied to remove trees which did not have commercial
value.
Kakamega Forest has a long history of exploitation (Mitchell 2004) and at present
forests of different physiognomic, successional and disturbance levels are found.
Most of the forests in Kakamega are middle-age secondary which are managed by
the Kenya Wildlife Service or the Forest Department. Forests of early seral stages
with high level of disturbance and indigenous and exotic plantations are also the
features of Kakamega Forest. Undisturbed primary forest is absent in Kakamega,
though some forests areas received greater protection and experienced little
disturbance.
Godere is the most disturbed among the three. The major disturbance in the forest
is selective cutting by timber industries, shifting cultivation by the indigenous
people, commercial coffee plantation by state and private enterprises and semi-
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
forest coffee management by the indigenous people and settlers. Therefore, the
forest in Godere is secondary with different level of anthropogenic disturbances.
While closed forest are absent in Godere, most of the remaining natural forests
are semi-open, so maintained for the growth of Coffea arabica under the system of
semi-coffee forest management. Under such system, competing trees, shrubs and
lianas are removed (Senbetta & Denich 2006) while shade species are
maintained.
Table 6.1 Some climatic and physiognomic characters of Godere, Budongo and
Kakamega forests
Altitude (m a.s.l.)
Mean
Godere
Budongo
Kakamega
1000-1500
950-1200
1460-1765
1200-1800
1343-2638
17-29
10.6-27.7
Transitional
Semi-deciduous
Dry
rainforest
tropical rainforest semi-evergreen
(Friis 1992)
(Reynolds 2005)
annual >1500
rain fall (mm)
Mean
annual 15-25
temperature (0C)
Forest type
perpipheral
Guineo-Congolian
transitional rainforest
(Althof 2005)
Floral elements
Afromontane,
Guineo-
Afromontane,
Guineo-Congolian,
Congolian
Guineo-Congolian,
Transitional
Transitional
logging, Selective logging, Logging (clear felling
Major
Selective
disturbance
shifting cultivation,
history (type)
semi-forest
silvicultural
coffee treatment
& selective), exotic
tree plantation
management,
commercial coffee
plantation
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
6.3 Methodology
The methodology followed for foliicolous lichen collection and identification is
presented in Chapter 2. In order to make comparison of α- and β-diversity of the
three forests simple, only taxa identified to species and subspecific level were
considered. Exception to this is Opegrapha sp. since it occurs in the three forests
and all the specimens are expected to belong to the same species. Alpha diversity
of foliicolous lichens is analysed from the observed species richness, species
accumulation curves, non-parametric species richness estimators (Colwell 2006)
and Shannon-Wiener diversity and evenness indices (Magurran 1988). Beta
diversity is computed with Whittaker index (Whittaker 1960) and Sørenson’s index
of similarity (Sørenson 1948). The frequency occurrences of species in the
samples of Godere, Budongo and Kakamega forests were analysed based on a
six-scale frequency classes (see section 2.3.1). Statistical analyses were done in
order to look for significant differences in α-diversity using Statigraphics version 5
software (Statistical Graphics Corporation).
Ordination of the forest sites and species of the three forests was made using
Principal Component Analysis (PCA) using the software CANOCO (ter Braak &
Šmilauer 2002). PCA is selected for ordination since the initial correspondence
analysis provided a gradient length of less than 3 indicating a linear response of
species distribution. In the PCA ordination centering by species was selected.
The PCA biplot is used to identify characteristic foliicolous lichen species that can
be used as indicator of forest types of different disturbance regimes. Species that
have high fidelity to a particular forest type with high frequency of occurrence were
then used as indicators of that forest type (disturbance regime). Only species
which occurred on all or most of the forest sites of a particular disturbance regime
are selected as indicator species.
Dufrene and Legendre (1997) called these
species as symmetrical indicators whose presence contributes to the habitat
specificity.
In order to establish the biogeographical distribution of the typically and
facultatively foliicolous lichen species of Ethiopia, Uganda and Kenya, data from
the present study as well as additional data for Kenya (Lücking and Kalb 2002)
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
and Uganda (Feuerer 2007) were utilized. Information on the distribution types of
the foliicolous lichens were obtained from Lücking et al. (2000), Lücking & Colin
(2004), and the observation of the present study. The biogeographical distribution
of foliicolous lichens is analysed based on the lichenogeographical regions of
Lücking (2003). The similarity in foliicolous lichens of Godere, Budongo and
Kakamega forests and Taϊ National Park in Ivory Coast is determined using
Sørensen similarity index (Sørensen 1948).
6.4 Results
6.4.1 α-diversity
6.4.1.1 Family, generic and species richness
A total of 16 families of foliicolous lichen were recorded from the three forests (Fig.
6.1). All of these families were represented in Kakamega while only 15 families
were recorded from Godere and Budongo. The family Monoblastiaceae was not
represented in Budongo and Microthyriaceae was not represented in Godere.
Forty-one genera were recorded from the three forests. Generic diversity is
highest in Kakamega (39 genera), the genera Caprettia and Eugeniella being
absent.
Thirty-three
genera
were
recorded
from
Budongo,
the
genera
Aderkomyces, Badimia, Caprettia, Enterographa, Eremothecella, Gyalideopsis,
Lasioloma, and Musaespora being absent. Godere ranks the least in generic
diversity (27 genera). The genera Aderkomyces, Aulaxina, Badimia, Bapalmuia,
Eugeniella,
Enterographa,
Eremothecella,
Gyalideopsis,
Lasioloma,
Lichenopeltella (lichenicolous fungi), Loflammia, Mazosia, Musaespora, and
Tricharia were not recorded from Godere.
In terms of species diversity, Kakamega and Budongo forests have higher number
of foliicolous lichen species diversity than Godere. The observed number of
species from Godere is 70, 125 from Budongo and 137 from Kakamega.
The mean number of species per sample in Godere Forest is 9.8, 10.7 in Budongo
and 11.1 in Kakamega (Fig. 6.2). Kruskal-Wallis one way ANOVA was performed
to see if there is significant difference among the three medians. The result
150
A Comparative Analysis of Godere, Budongo and Kakamega Forests
indicated absence of significant difference (Chi square = 4.08, p-value = 0.1298) at
95% confidence level.
Monoblastiaceae
Verrucariaceae
Thelotremataceae
Strigulaceae
Kakamega-Species
Kakamega-Genus
Budongo-Species
Roccellaceae
Ramalinaceae
Porinaceae
Budongo-Genus
Godere-Species
Godere-Genus
Pilocarpaceae
Microthyriaceae
Lyrommataceae
Gomphillaceae
Coenogoniaceae
Coccocarpiaceae
Asterothyriaceae
Aspidotheliaceae
Arthoniaceae
0
5
10
15
20
25
30
No. of taxa
Fig. 6.1 Number of genera and species per family in Godere, Budongo and
Kakamega forests
20
18
Mean no. of species
16
14
12
10
8
6
4
2
0
Godere
Budongo
Kakamega
Fig. 6.2 Mean (±SD) number of species per sample in Godere, Budongo and
Kakamega forests
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
The estimated number of species for Godere, Budongo and Kakamega by the
non-parametric species richness estimators is presented in Table 6.2. The second
order and first order Jackknife estimators respectively predicted the highest
richness for both forests and the Michaelis-Menten Means (MMMeans) predicted
the lowest species richness. The difference between the highest and the lowest
estimates is 13.3 species for Godere, 18.9 species for Budongo and 37.3 species
for Kakamega. The Michaelis-Menten Means estimator was not found to be a
good estimator for Kakamega as its estimate (135.6 species) is below the
observed number of species (138). According to these estimators more than 80%
of the foliicolous lichen species predicted were collected from Godere, Budongo
and Kakamega forests.
For Godere the species accumulation curves (not shown) of MMMeans and Jack 2
estimators seemed to approach an asymptote, the curves for the others either did
not approach an asymptote or did not stabilize. For Budongo, the species
accumulation curves of Jack 2 and MMMeans estimators approached a horizontal
asymptote. The curves for the other estimators did not approach an asymptote.
Therefore, for Godere and Budongo the estimates of MMMeans could be
considered as the lower limit of species richness and the Jack 2 estimates as the
upper limit. For Kakamega the curves for Jack 1 and Chao 2 estimators seem to
approach an asymptote. Accordingly the estimate of Chao 2 could be considered
as the lower limit of species richness and that of Jack 1 as the upper limit.
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
Table 6.2 Species richness estimates and other summary values for foliicolous
lichen species in Godere, Budongo and Kakamega forests
Godere
Budongo
Kakamega
No. of samples
64
194
304
No. of individuals
626
2068
3380
Sobs
71
126
138
75.6
128.1
135.6
78.95 ± 5.5
135.5 ± 5.8
159±11.6
Jackknife 1
85.8 ±4.4
144.9±4.4
169.9±6.1
Jackknife 2
88.9
146.97
172.9
ICE
82.6
138.8
156.4
Bootstrap
78.6
135.6
148.6
86-98
80-102
MMMeans
Chao 2
Collection degree (%)
80-94
6.4.1.2 Shannon diversity
Table 6.3 presents the Shannon diversity and evenness indices for the foliicolous
lichen species of Godere, Budongo and Kakamega forests. ANOVA followed by
Fischer’s least significant difference (LSD) post hoc test indicated significant
difference (F-value = 69.04, p<0.05) in Shannon diversity between Godere and
Budongo as well as Godere and Kakamega. There is no significant difference
between Budongo and Kakamega. Diversity of foliicolous lichens, as measured by
Shannon index, is therefore significantly higher in Budongo and Kakamega than in
Godere. The Shannon evenness is similar in Godere and Budongo but is slightly
lower in Kakamega.
Table 6.3 Shannon diversity and evenness of foliicolous lichens in Godere,
Budongo and Kakamega forests.
Shannon diversity index
Godere
Budongo
Kakamega
3.66
4.14
4.09
0.86
0.86
0.83
(H’)
Shannon evenness
index (J’)
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
6.4.2 Beta diversity
Beta diversity of foliicolous lichens, expressed as the number of species observed
divided by the mean number of species, is high in Kakamega and Budongo and
low in Godere (Table 6.4). As this index of β-diversity is a measure of the species
turnover or the degree of change in species composition, species turnover is high
in Kakamega and Budongo and low in Godere.
Table 6.4 Total β-diversity in Godere, Budongo and Kakamega forests
Total species Mean number of
species per sample
number
(b)
(a)
β-diversity
(a/b)
Godere
71
9.8
7.2
Budongo
126
10.7
11.8
Kakamega
138
11.1
12.4
The similarity in species composition, measured by Sørensen similarity index,
shows high foliicolous lichens similarity between Budongo and Kakamega than
between these forests and Godere (Table 6.5).
Table 6.5 Sørensen similarity index values for Godere, Budongo and Kakamega
Godere
Godere
Budongo
-
Budongo
0.59
-
Kakamega
0.61
0.77
6.4.3 Species frequency
In Godere, Budongo and Kakamega forests rare species constituted 62%, 74.6%
and 77.5% of the total species respectively (Fig. 6.3). Occasional species
constituted the next highest proportion. The species which fall in the other
frequency classes constituted very small proportion.
154
A Comparative Analysis of Godere, Budongo and Kakamega Forests
100%
90%
80%
Rare
70%
Occasional
60%
Less frequent
50%
Frequnet
40%
Very frequent
30%
Abundant
20%
10%
0%
Godere
Budongo
Kakamega
Fig. 6.3 Proportion (%) of species in the various frequency classes in Godere,
Budongo and Kakamega forests
In Godere, Porina epiphylla, P. nitidula, P. subpallescens, and P. rubentior were
the dominant species. Strigula phyllogena, Bacidina apiahica, and Calopadia
puiggarii were the very frequent species. Species classified as frequent were
Calopadia fusca, Gyalectidium filicinum, Porina cupreola var. cupreola, P.
leptosperma, and Strigula smaragdula. Fellhanera paradoxa, Gyalidea epiphylla,
Calenia
monospora,
Lyromma
nectandrae,
and
Trichothelium
africanum
constituted the less frequent class. The species classified as occasional were
Aspidothelium
fugiens,
Brasilicia
foliicola,
Byssolecania
hymenocarpa,
Coccocarpia stellata, Fellhanera bouteillei, Gyalectidium imperfectum, Strigula
nemathora var. hypothelia, Strigula nitidula, Trichothelium pauciseptatum and
Trichothelium minutum The remaining 44 species were rare. The frequency
occurrence of foliicolous lichens and lichenicolous fungi of Godere Forest is
presented in Appendix 3.
In Budongo Forest, only Porina epiphylla fall into the dominant frequency class.
Species classified as very frequent were Porina nitidula, P. radiata, P. rubentior,
Strigula phyllogena, S. smaragdula, and Coenogonium dilucidum. The frequent
species were Mazosia rotula, M. melanopthalma, Strigula nemathora var.
hypothelia and S. nitidula.
Porina sphaerocephala, P. alba, P. semicarpi and
Strigula microspora constituted the less frequent frequency class. Byssolecania
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
deplanata, Bacidina apiahica, Brasilicia foliicola, Byssolecania hymenocarpa,
Echinoplaca
pellicula,
Fellhanera
submicrommata,
Gyalectidium
filicinum,
Lyromma nectandrae, Porina conica, Porina cupreola var. cupreola, P.
epiphylloides, P. kamerunensis, P. leptosperma, P. rubescens, Sporopodium
leprieurii, Strigula multipunctata, and S. obducta were the species classified as
occasionals. The remaining species were classified as rare. The proportion of
species in the various frequency classes in Budongo Forest is presented in
Appendix 8.
In Kakamega Forest Porina nitidula, P. epiphylla, P. rubetior, and P. cupreola var.
cupreola were the dominant species. The very frequent species were Strigula
phyllogena, S. amaragdula and Porina subpallescens. Gyalectidium filicinum,
Strigula nitidula and Byssoloma leucoblepharum were the species classified as
frequent. Species classified as less frequent were Coenogonium geralense, C.
subluteum, Lyromma nectandrae, Calopadia puiggarii, Calenia monospora,
Strigula macrocarpa, and Trichothelium pauciseptatum. Bacidina apiahica,
Chroodiscus verrucosus, Coenogonium lisowskii, Coenogonium pocsii, C.
siquirrense,
Fellhanera
bouteillei,
Gyalectidium
caucasicum,
Mazosia
melanopthalma, Porina epiphylloides, P. rubescens, Strigula microspora, S.
nemathora var. hypothelia and S. obducta were the species classified as
occasional. The remaining species were rare. The frequency occurrence of
species in Kakamega Forest is presented in Appendix 13.
6.4.4 Ordination
Principal component analysis (PCA) biplot of the species by forest sites data
matrix of Godere, Budongo and Kakamega forests is presented in Fig. 6.4. The
first four axes of the PCA ordination explain 50.6% of the total variation in the
species data. The first and second axes of PCA ordination explain 21.7% and
13.8% of the total variation respectively; therefore most of the variation in species
composition is explained by the first axis. In the PCA biplot species are
represented by arrows and forest sites by dots. The direction of the arrow
indicates the direction in which the abundance of a species increases most rapidly.
The length of the arrows indicates the rate of change in abundance in that
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
direction. A long arrow indicates gradual rate of change in abundance, while a
short arrow represents very rapid change.
The distribution of the forest sites in the PCA biplot shows a clear pattern, with the
primary, swamp, old secondary and young secondary forests of Budongo showing
a strong positive correlation with the first axis but negative correlation with the
second axis. The forest sites of Isiukhu, Yala, Ikuywa, and Salazar are positively
correlated with both the first and the second axes but the correlation with the
second axis is stronger. The forest site of Buyangu is slightly positively correlated
with both axes while Kisere is slightly negatively correlated with the first axis and
positively correlated with the second axis. Isecheno, Bukhaywa, Busambuli and
Colobus forest sites of Kakamega are negatively correlated with the first axis and
positively with the second axis. The forest sites of Dushi, Bishan Waka, Kaimosi,
Malava, Ghostisland and Camp site are negatively correlated both with both the
first and the second axes. The distribution of the study sites along the first PCA
axis seems to depend on the level of forest disturbance. Therefore, forest sites
with a strong positive correlation with the first PCA axis are undisturbed or slightly
disturbed, while forest site negatively correlated with the first axis are more
disturbed.
157
1.0
A Comparative Analysis of Godere, Budongo and Kakamega Forests
BYSLE
GYACA
Isiukhu
STROB
CALMO
STRMA
Yala
COELICOEGE
Isecheno
CALSCPORRU
PORCU
OPEPH Ikuywa
CALPU
PORSU
SalazarCALGRPORED COEPO
Kisere
COEFL TRIPA
COESF
STRNI
ENTME
LYRNE SPOPI
STRMI
STRSM
COESI
Buyangu
TRIVA
GYAFI
Busambuli
Bukhayawa
COESL
BYSVA
PORSE
COESD
BRADI
BRAFO
COEUS
SPOLE
Axis 2
Colobus
CHRKA
FELBU
Swamp
BAPPA CHRAU
Kaimosi GYAES
GYAFU
ASTSE
SPOPH
ASTRO
BACAP
Dushi
GYAIM
COEPA
TRINI
TRIAL
STRJA
PORSP
MAZDI
PORKA PORLE
MAZRO
FELSM Young Sec.
PORCO
BYSHY BYSFU
BYSSP
MAZPH
STRMU
PORRA
Old Sec.
Primary
Bishan Waka
-1.0
Camp site
COEDI
BACMI BYSDE
PORSH
PSOVA
ASTAU
Ghostisland
BACPA
Malava TRISP
PSOPA PSOGY
ASTPI
FELSL
ASTLE
MAZME
-1.0
Axis 1
1.0
Fig. 6.4 PCA biplot of species and forest sites. Red circles = forest sites from
Godere, green = Budongo, yellow = Kakamega. For species acronym see
Appendix 16. For the purpose of clarity some of the species are omitted.
6.4.5 Foliicolous lichens as indicator of disturbance
Indicator species of forest types (disturbance regime) are determined from the
distribution of species along the first axis of PCA biplot (Fig. 6.4). Species with a
strong positive correlation with the first PCA axis are characteristic of undisturbed
closed forest. Species with a strong negative correlation with the first axis are
characteristic of a heavily disturbed forest site. The frequency of a species in the
various forest types is also consulted in order to select indicator species. Only
species restricted to a particular forest type with high frequency are considered as
indicator of that forest type. Based on the distribution of the species and forest
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
sites on the PCA biplot, the following species are selected as indicator of three
forest types with different disturbance regime.
1. Undisturbed/slightly disturbed closed forest. Forests of this type have
closed canopy with infrequent canopy openings. The primary, swamp, old
secondary and young secondary forests of Budongo belong to this group. The
predominant microsite in such forest types is shady understorey and species of
such microsite are more abundant than the other species (Table 6.6). Light gap
species constitute a very small proportion and canopy species are either absent or
very rare. Indicator species for this group are Porina sphaerocephala, Porina
conica, Porina radiata, and Mazosia rotula. These species are mostly confined to
the primary or old growth forests and have not been recorded from the middleaged and young secondary forests.
a
c
b
d
Fig. 6.5 Indicator species for undisturbed closed forest, (a) Mazosia rotula, (b)
Porina sphaerocephala, (c) Porina radiata, (d) Porina conica
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
Foliicolous lichens associated with this forest type include Mazosia phyllospora, M.
dispersa, Strigula janeriensis, S. multipunctata, Bysoloma fumosonigricans, B.
hymenocarpa, Chroodiscus australiensis, Porina leptosperma, P. kameruensis, P.
sphaerocephaloides, Fellhanera submicrommata, Byssoloma subpolychromum,
and Bapalmuia palmularis.
2. Closed forest with moderate disturbance. This is the largest forest type
where most of the forest sites of the study area belong. The forest canopy in this
group is largely closed, however irregular openings could be seen here and there.
Yala, Ikuywa, Salazar, Buyangu, Isiukhu, Isecheno, Colobus and Kisere forest
sites belong to this category. Forests under this group have most of the species
distributed both in the shady understorey and light gap microsites and very few
species in the canopy microsite (Table 6.5). Indicator species for this group are
Coenogonium geralense, Coenogonium siquirrense, Coenogonium pocsii, and
Byssoloma leucoblepharum.
a
b
c
d
Fig. 6.6 Indicator species for closed forest with moderate disturbance, (a)
Coenogonium geralense, (b) C. pocsii, (c) Byssoloma leucoblepharum, (d) C.
siquirrense.
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
Foliicolous lichens associated with this forest type include Coenogonium
subfallaciosum, C. subluteum, C. usambarense, C. pocsii, Brasilicia foliicola, B.
dimerelloides, Tricharia vainioi, Mazosia melanopthalna, Porina semicarpi, Porina
epiphylloides, Byssolecania variabilis and Sporopodium pilocarpoides.
3. Disturbed semi-open forest. The forests grouped under this type have semiopen canopy which allows light to reach the inside of the forest. Bukhaywa,
Busambuli, Ghostisland, Malava, Kaimosi, Dushi, Bishan Waka and Camp site
forests belong to this category. The foliicolous species composition is largely made
up of more of light gap species than shady understorey species. In the Camp site
forest which is more open than the other forest sites in this group, the proportion of
light gap species is very high (70%) and more canopy specialists are recorded in
the understorey (Table 6.6). Indicator species for the semi-open canopy forest
group
are
Asterothyrium
rotuliforme,
Psorotheciopsis
gyalideoides,
P.
varieseptata, Calenia aspidota and Gyalectidium imperfectum. Species associated
with this forest type include Fellhanera bouteillei, Asterothyrium aulaxinoides,
Fellhanera sublecanorina, and Calenia monospora.
a
b
c
d
Fig. 6.7 Indicators species for open forest, (a) Asterothyrium rotuliforme, (b)
Calenia aspidota, (c) Gyalectidium imperfectum, (d) Psorotheciopsis gyalideoides
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
Table 6.6.Proportion (%) of foliicolous lichen species of the forest sites of Godere,
Budongo and Kakamega in the forest microsites
Old secondary
Shady
Transition
understorey to light gap
38.6
26.3
Light
gap
29.8
Transition Outer
to canopy canopy
5.3
-
Isecheno
Primary
37
34.2
26.1
31.6
21.7
26.3
13
6.6
2.2
1.3
Kisere
Swamp
32.3
31.3
24.6
31.5
27.7
26.1
10.8
8.7
3.1
2.2
Ikuywa
Colobus
Yala
Young secondary
Dushi
Buyangu
Kaimosi
31.1
31.1
30.8
28
26.7
24.7
24.4
23
24.4
26.2
30.1
21.7
31.5
22
32.8
33.3
29
30.1
35
27.4
36.6
9.8
6.7
10.8
11.8
13.3
13.7
12.2
3.3
4.4
3.1
3.3
2.7
4.9
Isikuhu
Salazar
24.3
23.8
27
33.3
31.1
31.7
16.2
9.5
1.4
1.6
Ghostislanid
Bukhaywa
22.6
22.2
19.4
24.4
38.7
35.6
9.7
13.3
9.7
4.4
Bishan Waka
Busambuli
19.4
18.9
13.9
18.9
44.4
30.2
13.9
22.6
8.3
7.5
Malava
Camp site
17.1
7.4
19.5
3.7
41.5
37
14.6
25.9
7.3
25.9
6.4.6 Biogeographic affinity of the foliicolous lichens of the study area
Lücking (2003) distinguished 6 lichenogeographical regions for foliicolous lichens.
These are (1) Neotropics, (2) African Paleotropics, (3) Eastern Paleotropics, (4)
Valdivian region, (5) Tethyan region, and (6) Neozealandic-Tasmanian region.
About 57% of the foliicolous lichen species of Ethiopia, Uganda and Kenya were
pantropical being distributed in the three tropical regions (Latin America, Africa
and Southeast Asia). The African paleotropical species constituted 18.6% of the
total species. Seventeen per cent of the species had their distribution in the
African Paleotropics and the Neotropics, and are thus called Western Gondwana.
Paleotropical species have their distribution range in the African Paleotropics and
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
the Eastern Paleotropics and they constituted 7.2% of the whole species. About
1% of the species were cosmopolitan with distribution in the tropical regions as
well as in the extra tropical regions and 1 species had distribution range in the
African Paleotropics and Tethyan region.
African Paleotropics 18.6
Cosmopolitan 1%
Western Gondwana 17%
Paleotropics 7.2%
African-Tethyan 0.5%
Pantropics 56.7%
Fig. 6.5 Proportion of world distribution types of currently known foliicolous lichens
of Ethiopia, Uganda and Kenya
Thirteen species which had a recorded distribution outside Africa have been
recorded from Godere, Budongo and Kakamega forests for the first time and are
thus new records for Africa. These are Aspidothelium geminiparum, Asterothyrium
aulaxinoides,
pannosum,
Calenia
triseptata,
Coenogonium
Coenogonium
siquirrense,
barbatum,
Eugeniella
Coenogonium
wettsteinii,
Fellhanera
aurantiaca, Porina rubescens, Strigula microspora, and Trichothelium africanum.
All of these species were previously recorded from the Neotropics only.
Aspidothelium scutelicarpum was previously recorded from the Amphipacific
region (Neotropics and Eastern Paleotropics) and Coenogonium flavum which was
recorded from the Neotropics and Neozealandic-Tasmanian region are new
records for Africa.
In order to see if there is similarity in the foliicolous lichens of the study area with
other rainforests in Africa, the lowland tropical rainforest of Taϊ National Park in
Ivory Coast was considered (Lücking et al. 1998). Taϊ National Park, located in
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
southwestern Ivory Coast (Cote d’Ivoire) at altitudes 80-396 m, is the largest
undisturbed tropical rainforest in West Africa. Comparison of the 97 foliicolous
lichen species reported from this forest (Lücking et al. 1998) with our study area
provided 50 shared species and a Sørensen similarity index of 0.39. This low level
of similarity can be partly ascribed to the difference in disturbance conditions.
While the forests of our study area are found under different anthropogenic
disturbance conditions, the forest in Taϊ National Park is largely an undisturbed
primary rainforest (Santesson & Lücking 1999). The list of foliicolous lichen
species of Taϊ National Park did not contain species typical of open habitats.
6.5 Discussion
6.5.1 Foliicolous lichens diversity in Ethiopia, Uganda and Kenya
Lichens in general and foliicolous lichens in particular were overlooked both in
Ethiopia, Uganda and Kenya. The 70 species of foliicolous lichens and
lichenicolous fungi new to Ethiopia, 108 species new to Uganda and 77 species
new to Kenya recorded in this study from a single forest in each country is a clear
indication that high diversity of lichens could be expected in these countries. The
number of new species recorded from the three forests is considerably high. It is
worthmentioning that most of the new species were recorded from forest sites
affected by disturbance. The major reason for the under collection of lichens in
Africa is lack of expertise. Many African botanists prefer working on vascular
plants to cryptogams. Lack of reference material is also a bottleneck for research
in lichens. There is only one book (Swinscow and Krog 1988) available as a
reference material for the macrolichens of East African (Ethiopia, Uganda, Kenya
and Tanzania). For foliicolous lichens, however, no compiled reference material
has ever been prepared for Africa. Santesson (1952) and the various publications
after him are the only sources of information. There is therefore much work and
challenge ahead before the lichen flora of tropical Africa is fully revealed.
Comparison of the foliicolous lichens recorded in the present study with earlier
reports from the Neotropics, Southeast Asia and East and West Africa is made.
Diversity of foliicolous lichens is high in the neotropical rainforests. The Central
American rainforest, for example, harbours 390 species of foliicolous lichens
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
(Cáceres et al. 2000). At site level, high foliicolous lichen diversity is found at ‘’La
Selva’’, a lowland rainforest in Costa Rica, with 280 species of foliicolous lichens
and 18 species of lichenicolous fungi (Lücking 1999g), at ‘’Jatun Satcha, a lowland
rainforest in Ecuador, with 232 species of foliicolous lichens (Lücking 1999d) and
at the Botarrama trail, a premontane rainforest in Costa Rica, with 217 species of
typically foliicolous lichens (Lücking 1999f). From Guyana, Lücking (1998b)
reported 233 species of foliicolous lichens and 18 species of lichenicolous fungi.
From the Atlantic rainforest of Brazil, Cáceres et al. (2000) reported 191 species of
foliicolous lichens and 19 lichenocolous fungi on foliicolous lichens.
For Southeast Asia Papong et al. (2006) reported 8 species of foliicolous lichens
from Nepal, 53 species from Sri Lanka , 60 species from China, 70 species from
Vietnam, 83 species from Japan, 90 species from India, 106 species from
Thailand, 120 species from Indonesia, 120 species from Malaysia, 191 species
from Papua New Guinea, and 224 species from Philippines. In the continental
Australia, 202 species of foliicolous lichens have been reported (Lücking et al.
2001). The numbers of foliicolous lichens recorded from Kakamega and Budongo
forests are higher than the number of species reported from most of these tropical
countries. The number of foliicolous lichens recorded from Godere is higher than
the number reported at a country level for Nepal, Sri Lanka, China and Vietnam.
Comparison with reported species number from forest sites in Africa shows higher
species diversity in Budongo and Kakamega and comparable or low diversity in
Godere. Pócs (1978) reported 75 species from lowland and submontane
rainforests in Tanzania and Lücking et al. (1998) reported 98 species from a
lowland rainforest of Taϊ National Park in Ivory Coast.
Several studies have documented high foliicolous lichen diversity in undisturbed
primary forests compared to disturbed secondary forests (Lücking 1998b, Sipman
1991). Our results show high foliicolous lichen diversity in primary forest and in
secondary forests with relatively little disturbance. Although the large part of
Kakamega is secondary forest and is more disturbed than Budongo, at forest level
high foliicolous lichen species were recorded from the former than the latter. In
Budongo Forest, 100 species were recorded from the two primary forest sites and
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
118 species from the secondary forest sites. In Kakamega Forest comparable
numbers of foliicolous lichens were recorded from the secondary forest sites of
Yala (67 species), Buyangu (74 species) and Isiukhu (77 species) and the nearprimary forest site of Kisere (66 species). In the more disturbed secondary forest
sites of Kakamega (e.g. Malava, Kaimosi, Camp site) and in Godere Forest,
foliicolous lichen diversity is substantially reduced.
Since high diversity is recorded in forests with relatively low level of disturbance,
our observation is in line with the Intermediate Disturbance Hypothesis (Connell
1978). The diversity of an area is influenced by the type, frequency and intensity of
disturbance (Petraitis et al. 1989). Since the diversity and composition of
foliicolous lichens is dependent on the available microsite habitats in a forest, any
human impact that results in loss of habitat and significant change in the
microclimatic environment will inevitably affect the diversity of foliicolous lichens.
Clear-cutting and forest conversion to agricultural land use system, for example,
result in total or partial removal of the understorey and light gap microsites
resulting in a significant reduction of diversity. The effect on foliicolous lichen
diversity of local forest exploitation for example by pit-sawing or fuelwood
collection might be minimal. The impoverishment of foliicolous lichens in Godere
Forest is primarily due to the conversion of a natural forest to a semi-forest coffee
land use system. When understorey shrubs and lianas are removed under such
system, foliicolous lichens are also removed along with. Besides, the number of
available phorophyte individuals and species are limited, further diminishing the
diversity of foliicolous lichens. For maintaining foliicolous lichens diversity, semicoffee forest land use system is, however, much better than shifting cultivation and
conversion to permanent agriculture. Selective logging or pitsawing, on the other
hand, could enhance high foliicolous lichen diversity if the intensity and frequency
is very limited. These types of human activity have taken place in the secondary
forests of Budongo and the middle-age and old secondary forests of Kakamega;
nevertheless, foliicolous lichens diversity in these forest types is still high. In
contrast where the impact of disturbance was higher (e.g. Malava, Camp site,
Kaimosi forests of Kakamega and Godere Forest), the diversity of foliicolous
lichens is considerable reduced.
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
Tropical lowland and lower montane rainforests are most suitable habitats for
foliicolous lichens (Lücking 2001). Under natural conditions, high foliicolous lichens
diversity is expected from Godere, Budongo and Kakamega forests. The results
from our studies confirmed high diversity in Budongo and Kakamega forests which
is even higher than the diversity recorded for some countries in Southeast Asia.
6.5.2 Indicator species
Lichens have been found to be sensitive to anthropogenic disturbance and are
useful indicators of ecological change (Nimis et al. 2002). The use of lichens as
bioindicator lies in their poiklohydrous physiological conditions and symbiotic
nature. Metabolic processes such as photosynthesis, nitrogen fixation, mineral
accumulation, and growth rate in lichens vary in response to seasonal and
environmental changes (Galloway 1992, Renhorn et al. 1997). Any environmental
change that damages either the fungal or the algal partner results in a breakdown
of the symbiosis and ultimately to the death of the lichen (Nimis & Purvis 2002)
Several studies (Wolseley and Aguirre-Hudson 1991, Wolseley and AguirreHudson 1997, Mistry 1998, Wolseley 2002, Holz 2003, Nöske 2004, Saipunkaew
et al. 2005, Plata et al. 2007) have demonstrated the potential of lichens as
indicators of environmental changes in tropical areas. Furthermore, foliicolous
lichens have been shown to have a high potential as bioindicators of altitudinal
zonation (Pocs 1977, Lücking 1995b, Herrera-Campos et al. 2004, Alejandrina et
al. 2007), microclimate (Lücking 1994), seasonality (Sérusiaux & De Sloover 1986,
Lücking 1995b), anthropogenic disturbances (Lücking 1995a, Lücking 1997d),
biodiversity (Lücking 1995b) and biogeographic affinity (Lücking & Kalb 2001).
Lücking (2000) discussed the characters that make foliicolous lichens useful as
bioindicator. Their relationship to the living leaf is reduced, their dependence on
atmospheric factors are high, they have an accelerated life cycle and respond
rapidly to environmental changes, there are taxonomically better known and they
are particularly useful for ex-situ evaluation, since they are easily collected in large
quantities and quickly processed for investigation and documentation.
The distribution of foliicolous lichens within a given forest is largely dependent on
microsites (Lücking 1997d). The structure of a forest affects the distribution of
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
foliicolous lichens through its influence on the moisture and light regime in the
microsite. In a tropical lowland forest three microsites and two transitions are
recognized (Lücking 1997d). These are shady understorey, transition to light gap,
light gap, transition to outer canopy and outer canopy. Corresponding to these
microsite habitats, foliicolous lichens form three well-defined associations.
In the forest sites of our study area foliicolous lichens belonging to the genera
Arthonia
(Arthoniaceae),
(Pilocarpaceae),
Bapalmuia,
Coenogonium
Brasilicia,
(Coenogoniaceae),
Byssolecania,
Enterographa,
Fellhanera
Mazosia
(Roccellaceae), Porina, Trichothelium (Porinaceae) and Strigula phyllogena, and
S. obducta (Strigulaceae) belong to the shady understorey microsites. Except the
family Pilocarpaceae which has Chlorococcaceae photobiont, all the other families
have Trentepohliaceae photobiont.
Foliicolous lichen species belonging to the genera Calenia, Gyalectidium,
Echinoplaca (Gomphillaceae), Strigula smaragdula, S. nemathora, S. antillarum
(Strigulaceae), Calopadia, Tapellaria, Loflammia, and Lasioloma (Pilocarpaceae)
dominate the light gap microsite. These genera, except Strigula, have
Chlorococcaceae photobiont. The outer canopy microsite is dominated by the
genera
Asterothyrium
and
Psorotheciopsis
(Asterothyriaceae)
with
Chlorococcaceae photobiont. Our results are in consistence with the observation
of Lücking (1995c, 1999e) who recorded foliicolous lichen species of the family
Arthoniaceae, Opegraphaceae (=Roccellaceae), Trichotheliaceae (=Porinaceae)
and Pilocarpaceae (pycnidia bearing members) in the shady understorey, and
Gomphillaceae
and
Ectolechiaceae
(=campylidia
bearing
members
of
Pilocarpaceae) in the light gap.
The difference in foliicolous lichens composition in the various microsites is due to
light regime (Lücking 1999e). Foliicolous lichens exhibit ecomorphological
adaptations to the light regime. Foliicolous lichens in the shady understorey have
thin thalli with smooth surface (e.g. species of Arthonia, Bapalmuia, Brasilicia,
Trichothelium, Mazosia phyllosema, Porina epiphylla, P. rufula, P. rubescens) or
are
provided
with
small
verrucae
(e.g.
Porina
sphaerocephala,
P.
sphaerocephaloides, P. mazosoides, P. radiata, Mazosia rotula).
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
Foliicolous lichens in the light gap and outer canopy microsites have dispersed
and white thalli (e.g. species of Calopadia, Lasioloma arachnoideum, Loflammia
epiphylla) black apothecia (e.g. species of Tapellaria) and the phtobiont is
Trebouxia (Chlorococcaceae). The white thallus reflects light reaching the surface
of the thallus thereby reducing excessive loss of evaporation. In addition the thalli
of foliicolous lichens in the outer canopy have cortex made from dead cells e.g.
species of Asterothyrium and Psorotheciopsis).
The use of foliicolous lichens as indicator of forest disturbance lies in their
compositional differentiation in the different forest microsites. In undisturbed forest,
the canopy is closed and the amount of light intensity reaching the understorey
vegetation is very small and the moisture content is high. Under such condition,
foliicolous lichens adapted to the low light intensity become abundant, the
proportion of light gap species is very small and the proportion of canopy species
is negligible. In the Primary and Swamp forest of Budongo, for example, more
than 60% of the species belong to the shady understorey and the transition to light
gap microsites. The most frequent species in the shady understorey of the
undisturbed and moderately disturbed group of forest are Arthonia lividula,
Brasilicia dimerelloides, B. foliicola, Coenogonium pocsii, C. siquirrense, C.
subfallaciosum, Mazosia melanopthalma and Opegrapha velata (lichenicolous).
When a disturbance occurs in a forest, for example by selective logging, canopy
opening allows high light intensity to reach the understorey and this results in
reduced moisture content in the understorey. While shady understorey species
find these conditions unfavorable for their development, the conditions become
favorable for the growth of light gap species. Under extreme condition of
disturbance, where the canopy is widely opened, foliicolous lichens adapted to the
outer canopy could grow in the understorey. About 22% of the foliicolous lichen
species recorded from the understorey of Camp site forest of Kakamega are
canopy specialists. All the foliicolous lichen species recorded from the canopy tree
of Ficus lutea in Susungiru in Uganda have been recorded in the understorey of
Camp site forest.
The degree of forest disturbance can be inferred from the proportional abundance
of species in the different light regime of a forest. Occurrence of species of the
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
outer canopy (e.g. Asterothyrium leucophthalmum, A. monsporum, Calenia
monosora,
C.
aspidota,
Psorotheciopsis
gyalideoides,
Psorotheciopsis
patellarioides, Psorotheciopsis varieseptata) in the understorey is a clear
indication of wider canopy opening and thus severe forest disturbance. High
proportional abundance of species like Calopadia puiggarii, Fellhanera bouteillei,
Gyalectidium caucasicum, G. microcarpum, Lasioloma arachnoideum, and
Strigula antillarum in the understorey is an indication of moderate forest
disturbance, for example by selective logging or pitsawing resulting in partial or
irregular canopy openings.
6.5.3 Biogeography
Among the three tropical lichenogeographical regions, Africa is poor in foliicolous
lichens. Lücking (2003) reported 539 species from the Neotropics, 403 from
Eastern Paleotropics and 309 from the African Paleotropics. Meggers et al. (1973)
compared the epiphytic diversity of tropical Africa and South America and
indicated that the low epiphytic diversity in Africa is due to paleoclimatic dry
periods. It is not known whether the low number of foliicolous lichen species in
Africa is due to paleoclimatic conditions or due to insufficient collection. Since
many areas of Africa have not been investigated for their foliicolous lichen flora,
appropriate explanation for their diversity should be preceded by a thorough
collection of different forest types. The 7 new species recorded from the three
forests as well as those collections which are expected to belong to new species
and the 13 new records for Africa are clear indicators that the foliicolous lichen
flora of tropical Africa is under collected.
Santesson & Lücking (1999) analysed the world distribution pattern of the
foliicolous lichen flora of Ivory Coast. They found out that 56.5% of the species
had
pantropical
distribution,
22.4%
Western
Gondwana,
8.7%
African
Paleotropical, and 6.8% Paleotropical. Foliicolous lichens are known for their wide
distribution and high proportion of pantropical species were recorded from
collections made in different areas (Santesson & Lücking 1999, Cáceres et al.
2000, Herrere-Campos et al. 2004).
The proportion of pantropical and
paleotropical species in Ivory Coast and in Ethiopia, Uganda and Kenya are
similar. However, higher proportion of Western Gondwana species and lower
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
proportion of African Paleotropical species were recorded from Ivory Coast than
from the three countries investigated in this study. The new species of foliicolous
lichens described from the present study have contributed for the increased
proportion of the African paleotropical species of the three countries. The low
proportion of Western Gondwana species in our study area as compared to those
from Ivory Coast indicates that the foliicolous lichen flora of the Ivory Coast is
more similar to the flora of Neotropical rainforests than to the flora of the East
African rainforests.
The proportion of species common to the African Paleotropics and the Neotropics
is more than twice as much as those shared between the African and Eastern
Paleotropics. From the foliicolous lichens collected from Ivory Coast, Santesson &
Lücking (1999) reported that the Western Gondwana species were three times
more than the paleotropical species, indicating higher affinity of the African
foliicolous lichens to the Neotropical counterparts. Lücking et al. (1998) proposed
further study to determine whether this observed similarity is due to
paleogeographical relationships between the tropical Africa and tropical South
America or due to long distance dispersal.
6.6 Conclusion
The foliicolous lichen flora of Godere, Budongo and Kakamega forests has been
found to be considerably high. The number of species recorded especially from
Budogo and Kakamega are substantially higher than the species recorded at a
country level for many of the tropical countries in Southeast Asia. The numbers of
new species science and new records for Africa discovered in this study are
indicative that the foliicolous lichens flora of tropical Africa is insufficiently known.
The result of the present study predicts high foliicolous lichen diversity in the
tropical forests of Africa should such forests are investigated in detail. Therefore it
is recommended that more floristic and ecological study should be done especially
in the lowland and submontane rainforests of Africa.
At forest level, high foliicolous lichen diversity has been recorded from Kakamega
Forest than from Budongo and Godere. It is assumed that the diversity of forest
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A Comparative Analysis of Godere, Budongo and Kakamega Forests
type with different seral stages and disturbance levels has contributed for the
diversity of foliicolous lichens in Kakamega Forest. At site level, the forest sites of
Budongo have high foliicolous lichen diversity than the forest sites of Kakamega
and Godere. Secondary forests with low level of disturbance have been shown to
support similar foliicolous lichen diversity like primary forests. Therefore, for the
maintenance of high foliicolous lichen diversity in tropical Africa both primary and
old growth secondary forests should be conserved.
Due to differences in light intensity and moisture level the composition of
foliicolous lichens in the various microsites has been shown to be different. Forest
disturbance affects the structure of a forest which in turn affects the environmental
conditions in the microsites. Therefore, by observing the composition of foliicolous
lichen flora of a given forest site, it is possible to predict the degree of human
disturbance in the forest. In addition, some foliicolous lichens have been found to
be restricted to a particular microsite making them useful as bioindicator of
anthropogenic forest disturbance.
Therefore, the identification of indicator
foliicolous lichens could provide a basis for management recommendation in areas
of disturbed and fragmented forests in tropical Africa.
Most of the foliicolous lichen flora of the study has pantropical distribution and
more similar to the Neotropical flora than the Eastern Paleotropical flora. As a
result of the new species discovered in this study, the proportion of the African
Paleotropical species has ncreased.
172
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196
Appendices
Appendix 1. Foliicolous lichens and lichenicolous fungi from Godere Forest
Acronym
ARTAT
ARTLI
ASPFU
ASPHI
ASTLE
ASTMI
ASTOC
ASTRO
BACAP
BACMI
BACPA
BRAFO
BYSHY
BYSCH
BYSLE
BYSSU
CALMO
CALSP
CALTR
CALFU
CALPH
Species
Arthonia atropunctata Vain.
Arthonia lividula Vain.
Aspidothelium fugiens (Müll. Arg.) R. Sant.
Aspidothelium hirustum sp. nov.
Asterothyrium leucophthalmum (Müll. Arg.) R. Sant.
Asterothyrium microsporum R. Sant.
Asterothyrium octomerum R. Sant.
Asterothyrium rotuliforme (Müll. Arg.) Sérus.
Bacidina apiahica (Müll. Arg.) Vezda
Bacidina mirabilis (Vezda) Vezda
Bacidina pallidocarnea (Müll. Arg.) Vezda
Brasilicia foliicola (Vezda) Lücking, Kalb & Sérus.
Byssolecania hymenocarpa (Vain.) Kalb, Vezda & Lücking
Byssoloma chlorinum (Vain.) Zahlbr.
Byssoloma leucoblepharum (Nyl.) Vain.
Byssoloma subpolychromum Vezda
Calenia monospora Vezda
Calenia sp.
Calenia triseptata Zahlbr.
Calopadia fusca (Müll. Arg.) Vezda
Calopadia phyllogena (Müll. Arg.) Vezda
Family
Arthoniaceae
Arthoniaceae
Aspidotheliaceae
Aspidotheliaceae
Asterothyriaceae
Asterothyriaceae
Asterothyriaceae
Asterothyriaceae
Ramalinaceae
Ramalinaceae
Ramalinaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Gomphillaceae
Gomphillaceae
Gomphillaceae
Pilocarpaceae
Pilocarpaceae
Growth habit
Lichenicolous fungi
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
197
Acronym
CALPU
CAPSP
CHRSP
CHRVE
COCST
COEDI
COESU
COEUS
ECHPE
FELAU
FELBO
FELCF
FELPA
FELSF
FELSL
FELSM
GYAFI
GYAFU
GYAIM
GYAEP
LYRNE
OPESP
OPEVE
PHYPO
PORCF
PORCU
POREP
Species
Calopadia puiggarii (Müll. Arg.) Vezda
Caprettia goderei sp. nov.
Chroodiscus kakamegensis sp. nov.
Chroodiscus verrucosus R. Sant., Lücking & Vezda
Coccocarpia stellata Tuck.
Coenogonium dilucidum (Kremp.) Kalb & Lücking
Coenogonium subluteum (Rehm) Kalb & Lücking
Coenogonium usambarense (Vezda & Farkas) Lücking & Kalb
Echinoplaca pellicula (Müll. Arg.) R. Sant.
Fellhanera cf. aurantiaca (Vezda) Vezda
Fellhanera bouteillei (Desm.) Vezda
Fellhanera aff. bouteillei (Desm.) Vezda
Fellhanera paradoxa (Vezda) Vezda
Fellhanera subfuscatula Lücking
Fellhanera sublecanorina (Nyl.) Vezda
Fellhanera submicrommata (Vezda) Lücking & Kalb
Gyalectidium filicinum Müll. Arg.
Gyalectidium fuscum Lücking & Sérus.
Gyalectidium imperfectum Vezda
Gyalidea epiphylla Vezda
Lyromma nectandrae Bat. & H. Maia
Opegrapha sp.
Opegrapha velata (Müll. Arg.) Vain.
Phylloblastia pocsii (Farkas & Vezda) Lücking
Porina cf. triseptata (Vezda) Lücking
Porina cupreola (Müll. Arg.) F. Schill. var. cupreola
Porina epiphylla (Fée) Fée
Family
Pilocarpaceae
Monoblastiaceae
Thelotremataceae
Thelotremataceae
Coccocarpiaceae
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Gomphillaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Gomphillaceae
Gomphillaceae
Gomphillaceae
Asterothyriaceae
Lyrommataceae
Roccellaceae
Roccellaceae
Verrucariaceae
Porinaceae
Porinaceae
Porinaceae
Growth habit
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Facultative foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Ubiquotus
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Lichenicolous fungi
Lichenicolous fungi
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
198
Acronym
PORLE
PORNI
PORRU
PORRB
PORRF
PORSU
PORTE
PORTI
PSOPA
PSOVA
SPOAN
SPOLE
SPOPH
SPOSP
STRMA
STRMI
STRHY
STRNE
STRNI
STRPH
STRSC
STRSM
TAPBI
TRIAF
TRIEP
TRISP
TRIPA
Species
Porina leptosperma Müll. Arg.
Porina nitidula Müll. Arg.
Porina rubentior (Stirt.) Müll. Arg.
Porina rubescens (Lücking) Hafellner & Kalb
Porina rufula (Kremp.) Vain.
Porina subpallescens Vezda
Porina tetramera (Malme) R. Sant.
Porina trichothelioides R. Sant.
Psorotheciopsis patellarioides (Rehm) R. Sant.
Psorotheciopsis varieseptata (Vezda) Henssen & Lücking
Sporopodium antonianum Elix, Lumbsch & Lücking
Sporopodium leprieurii Mont.
Sporopodium phyllocharis (Mont.) Massal.
Sporopodium sp.
Strigula macrocarpa Vain.
Strigula microspora Lücking
Strigula nemathora var. hypothelia (Nyl.) R. Sant.
Strigula nemathora Mont.
Strigula nitidula Mont.
Strigula phyllogena (Müll. Arg.) R. C. Harris
Strigula schizospora R. Sant.
Strigula smaragdula Fr.
Tapellaria bilimbioides R. Sant.
Trichothelium africanum Lücking
Trichothelium epiphyllum Müll. Arg.
Trichothelium minutum (Lücking) Lücking
Trichothelium pauciseptatum Vezda
Family
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Asterothyriaceae
Asterothyriaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Pilocarpaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Growth habit
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
199
Appendix 2. Distribution of foliicolous lichens and lichenicolous fungi in Bishan
Waka and Dushi. 1 = present, 0 = absent
Bishan
Waka
Dushi
Arthonia atropunctata Vain.
0
1
Arthonia lividula Vain.
0
1
Aspidothelium fugiens (Müll. Arg.) R. Sant.
1
1
Aspidothelium hirustum sp. nov.
0
1
Asterothyrium leucophthalmum (Müll. Arg.) R. Sant.
1
0
Asterothyrium microsporum R. Sant.
0
1
Asterothyrium octomerum R. Sant.
0
1
Asterothyrium rotuliforme (Müll. Arg.) Sérus.
1
1
Bacidina apiahica (Müll. Arg.) Vezda
1
1
Bacidina mirabilis (Vezda) Vezda
0
1
Bacidina pallidocarnea (Müll. Arg.) Vezda
1
1
Brasilicia foliicola (Vezda) Lücking, Kalb & Sérus.
0
1
Byssolecania hymenocarpa (Vain.) Kalb, Vezda & Lücking
0
1
Byssoloma chlorinum (Vain.) Zahlbr.
0
1
Byssoloma leucoblepharum (Nyl.) Vain.
0
1
Byssoloma subpolychromum Vezda
0
1
Calenia monospora Vezda
1
1
Calenia sp.
0
1
Calenia triseptata Zahlbr.
0
1
Calopadia fusca (Müll. Arg.) Vezda
1
1
Calopadia phyllogena (Müll. Arg.) Vezda
0
1
Calopadia puiggarii (Müll. Arg.) Vezda
1
1
Caprettia goderei sp. nov.
0
1
Chroodiscus kakamegensis sp. nov.
0
1
Chroodiscus verrucosus R. Sant., Lücking & Vezda
1
1
Coccocarpia stellata Tuck.
1
1
Coenogonium dilucidum (Kremp.) Kalb & Lücking
0
1
Coenogonium subluteum (Rehm) Kalb & Lücking
0
1
Coenogonium usambarense (Vezda & Farkas) Lücking & Kalb
0
1
Echinoplaca pellicula (Müll. Arg.) R. Sant.
1
0
Fellhanera cf. aurantiaca (Vezda) Vezda
0
1
Fellhanera bouteillei (Desm.) Vezda
1
1
Fellhanera aff. bouteillei
1
0
Fellhanera paradoxa (Vezda) Vezda
1
1
Fellhanera subfuscatula Lücking
0
1
Fellhanera sublecanorina (Nyl.) Vezda
1
1
Fellhanera submicrommata (Vezda) Lücking & Kalb
0
1
Gyalectidium filicinum Müll. Arg.
1
1
Gyalectidium fuscum Lücking & Sérus.
1
0
Species
200
Bishan
Waka
Dushi
Gyalectidium imperfectum Vezda
1
1
Gyalidea epiphylla Vezda
1
1
Lyromma nectandrae Bat. & H. Maia
0
1
Opegrapha sp.
0
1
Opegrapha velata (Müll. Arg.) Vain.
0
1
Phylloblastia pocsii (Farkas & Vezda) Lücking
1
0
Porina cf. triseptata (Vezda) Lücking
1
1
Porina cupreola (Müll. Arg.) F. Schill. var. cupreola
1
1
Porina epiphylla (Fée) Fée
1
1
Species
Porina leptosperma Müll. Arg.
1
1
Porina nitidula Müll. Arg.
1
1
Porina rubentior (Stirt.) Müll. Arg.
1
1
Porina rubescens (Lücking) Hafellner & Kalb
0
1
Porina rufula (Kremp.) Vain.
0
1
Porina subpallescens Vezda
1
1
Porina tetramera (Malme) R. Sant.
0
1
Porina trichothelioides R. Sant.
0
1
Psorotheciopsis patellarioides (Rehm) R. Sant.
1
0
Psorotheciopsis varieseptata (Vezda) Henssen & Lücking
0
1
Sporopodium antonianum Elix, Lumbsch & Lücking
0
1
Sporopodium leprieurii Mont.
0
1
Sporopodium phyllocharis (Mont.) Massal.
1
1
Sporopodium sp.
0
1
Strigula macrocarpa Vain.
0
1
Strigula microspora Lücking
0
1
Strigula nemathora var. hypothelia (Nyl.) R. Sant.
1
1
Strigula nemathora Mont.
1
0
Strigula nitidula Mont.
1
1
Strigula phyllogena (Müll. Arg.) R. C. Harris
1
1
Strigula schizospora R. Sant.
0
1
Strigula smaragdula Fr.
1
1
Tapellaria bilimbioides R. Sant.
0
1
Trichothelium africanum Lücking
1
1
Trichothelium epiphyllum Müll. Arg.
1
1
Trichothelium minutum
1
1
Trichothelium pauciseptatum Vezda
1
1
201
Appendix 3. Frequency of occurrence of species in the samples of Godere Forest
Species
Arthonia atropunctata
Arthonia lividula
Aspidothelium fugiens
Aspidothelium hirsutum sp. nov.
Asterothyrium leucophthalmum
Asterothyrium microsporum
Asterothyrium octomerum
Asterothyrium rotuliforme
Bacidina apiahica
Bacidina mirabilis
Bacidina pallidocarnea
Brasilicia foliicola
Byssolecania hymenocarpa
Byssoloma chlorinum
Byssoloma leucoblepharum
Byssoloma subpolychromum
Calenia monospora
Calenia sp.
Calenia triseptata
Calopadia fusca
Calopadia phyllogena
Calopadia puiggarii
Caprettia goderei sp. nov.
Chroodiscus kakamegensis sp. nov.
Chroodiscus verrucosus
Coccocarpia stellata
Coenogonium dilucidum
Coenogonium subluteum
Coenogonium usambarense
Echinoplaca pellicula
Fellhanera aurantiaca
Fellhanera bouteillei
Fellhanera aff. bouteillei
Fellhanera paradoxa
Fellhanera subfuscatula
Fellhanera sublecanorina
Fellhanera submicrommata
Gyalectidium filicinum
Gyalectidium fuscum
Gyalectidium imperfectum
Frequency
Rare
Rare
Occasional
Rare
Rare
Rare
Rare
Rare
Very frequent
Rare
Rare
Occasional
Occasional
Rare
Rare
Rare
Less frequent
Rare
Rare
Frequent
Rare
Very frequent
Rare
Rare
Rare
Occasional
Rare
Rare
Rare
Rare
Rare
Occasional
Rare
Less frequent
Rare
Rare
Rare
Frequent
Rare
Occasional
202
Species
Gyalidea epiphylla
Lyromma nectandrae
Opegrapha sp.
Opegrapha velata
Phylloblastia pocsii
Porina cf. triseptata
Porina cupreola var. cupreola
Porina epiphylla
Porina leptosperma
Porina nitidula
Porina rubentior
Porina rubescens
Porina rufula
Porina subpallescens
Porina tetramera
Porina trichothelioides
Psorotheciopsis patellarioides
Psorotheciopsis varieseptata
Sporopodium antonianum
Sporopodium leprieurii
Sporopodium phyllocharis
Sporopodium sp.
Strigula macrocarpa
Strigula microspora
Strigula nemathora var. hypothelia
Strigula nemathora
Strigula nitidula
Strigula phyllogena
Strigula schizospora
Strigula smaragdula
Tapellaria bilimbioides
Trichothelium africanum
Trichothelium epiphyllum
Trichothelium minutum
Trichothelium pauciseptatum
Frequency
Less frequent
Less frequent
Rare
Rare
Rare
Rare
Frequent
Dominant
Frequent
Dominant
Dominant
Rare
Rare
Dominant
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Occasional
Rare
Occasional
Very frequent
Rare
Frequent
Rare
Less frequent
Rare
Occasional
Occasional
203
Appendix 4. Frequency of occurrence of species in the forest site of Dushi in
Godere forest
Species
Aspidothelium fugiens
Asterothyrium leucophthalmum
Asterothyrium rotuliforme
Bacidina apiahica
Bacidina pallidocarnea
Calenia monospora
Calopadia fusca
Calopadia puiggarii
Chroodiscus verrucosus
Coccocarpia stellata
Echinoplaca pellicula
Fellhanera bouteillei
Fellhanera aff. bouteillei
Fellhanera paradoxa
Fellhanera sublecanorina
Gyalectidium filicinum
Gyalectidium fuscum
Gyalectidium imperfectum
Gyalidea epiphylla
Phylloblastia pocsii
Porina cf. triseptata
Porina cupreola var. cupreola
Porina epiphylla
Porina leptosperma
Porina nitidula
Porina rubentior
Porina subpallescens
Psorotheciopsis patellarioides
Sporopodium phyllocharis
Strigula nemathora var. hypothelia
Strigula nemathora
Strigula nitidula
Strigula phyllogena
Strigula smaragdula
Trichothelium africanum
Trichothelium pauciseptatum
Trichothelium epiphyllum
Trichothelium minutum
Frequency
Rare
Occasional
Occasional
Frequent
Rare
Less frequent
Frequent
Dominant
Rare
Occasional
Rare
Less frequent
Rare
Very frequent
Rare
Dominant
Occasional
Rare
Occasional
Rare
Rare
Rare
Dominant
Occasional
Dominant
Occasional
Dominant
Rare
Rare
Rare
Rare
Rare
Dominant
Less frequent
Occasional
Rare
Rare
Rare
204
Appendix 5. Frequency of occurrence of species in the forest site of Dushi in
Godere forest
species
Arthonia atropunctata
Arthonia lividula
Aspidothelium fugiens
Aspidothelium hirsutum sp. nov.
Asterothyrium microsporum
Asterothyrium octomerum
Asterothyrium rotuliforme
Bacidina apiahica
Bacidina mirabilis
Bacidina pallidocarnea
Brasilicia foliicola
Byssolecania hymenocarpa
Byssoloma chlorinum
Byssoloma leucoblepharum
Byssoloma subpolychromum
Calenia monospora
Calenia sp.
Calenia triseptata
Calopadia fusca
Calopadia phyllogena
Calopadia puiggarii
Caprettia goderei sp. nov.
Chroodiscus kakamegensis sp. nov.
Chroodiscus verrucosus
Coccocarpia stellata
Coenogonium dilucidum
Coenogonium subluteum
Coenogonium usambarense
Fellhanera bouteillei
Fellhanera cf. aurantiaca
Fellhanera paradoxa
Fellhanera subfuscatula
Fellhanera sublecanorina
Fellhanera submicrommata
Gyalectidium filicinum
Gyalectidium imperfectum
Gyalidea epiphylla
Lyromma nectandrae
Opegrapha sp.
Frequency
Rare
Rare
Less frequent
Rare
Rare
Rare
Rare
Very frequent
Rare
Rare
Occasional
Occasional
Rare
Rare
Rare
Occasional
Rare
Rare
Frequent
Rare
Less frequent
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Occasional
Rare
Less frequent
Occasional
Rare
Occasional
Occasional
Occasional
Frequent
Frequent
Rare
205
species
Opegrapha velata
Porina cf. triseptata
Porina cupreola var. cupreola
Porina epiphylla
Porina leptosperma
Porina nitidula
Porina rubentior
Porina rubescens
Porina rufula
Porina subpallescens
Porina tetramera
Porina trichothelioides
Psorotheciopsis varieseptata
Sporopodium antonianum
Sporopodium leprieurii
Sporopodium phyllocharis
Sporopodium sp.
Strigula macrocarpa
Strigula microspora
Strigula nemathora var. hypothelia
Strigula nitidula
Strigula phyllogena
Strigula schizospora
Strigula smaragdula
Tapellaria bilimbioides
Trichothelium africanum
Trichothelium epiphyllum
Trichothelium minutum
Trichothelium pauciseptatum
Frequency
Rare
Rare
Dominant
Dominant
Very frequent
Dominant
Dominant
Rare
Rare
Dominant
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Occasional
Occasional
Frequent
Rare
Frequent
Rare
Less frequent
Rare
Occasional
Occasional
206
Appendix 6. Foliicolous lichens and lichenicolous fungi from Budongo Forest
Acronym
ARTLI
ARTOR
ASPFU
ASPGE
ASTMI
ASTMO
ASTPI
ASTRO
ASTSE
AULMI
BACAP
BACMI
BACPA
BACSI
MAPIV
MAPPA
BIASP
BRADI
BRAFO
BYSDE
BYSFU
BYSHY
BYSVA
Species
Arthonia lividula Vain.
Arthonia orbygniae (H. B. P. Upadhyay) Matzer
Aspidothelium fugiens (Müll. Arg.) R. Sant.
Aspidothelium geminiparum (Malme) R. Sant.
Asterothyrium microsporum R. Sant.
Asterothyrium monosporum Müll. Arg.
Asterothyrium pittieri Müll. Arg.
Asterothyrium rotuliforme (Müll. Arg.) Sérus.
Asterothyrium septemseptatum ssp. africanum Lücking & Kalb
Aulaxina microphana (Vain.) R. Sant.
Bacidina apiahica (Müll. Arg.) Vezda
Bacidina mirabilis (Vezda) Vezda
Bacidina pallidocarnea (Müll. Arg.) Vezda
Bacidina simplex Farkas & Vezda
Bapalmuia ivoriensis R. Sant. & Lücking
Bapalmuia palmularis (Müll. Arg.) Sérus.
Biatora sp.
Brasilicia dimerelloides (Vezda) Lücking, Kalb & Sérus.
Brasilicia foliicola (Vezda) Lücking, Kalb & Sérus.
Byssolecania deplanata (Müll. Arg.) R. Sant.
Byssolecania fumosonigricans (Müll. Arg.) R. Sant.
Byssolecania hymenocarpa (Vain.) Kalb, Vezda & Lücking
Byssolecania variabilis (Vain.) Kalb, Vezda & Lücking
Family
Arthoniaceae
Arthoniaceae
Aspidotheliaceae
Aspidotheliaceae
Asterothyriaceae
Asterothyriaceae
Asterothyriaceae
Asterothyriaceae
Asterothyriaceae
Gomphillaceae
Ramalinaceae
Ramalinaceae
Ramalinaceae
Ramalinaceae
Pilocarpaceae
Pilocarpaceae
Bacidiaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Growth habit
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Facultative foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
207
Acronym
BYSCH
BYSLE
BYSSD
BYSSP
CALAS
CALBU
CALDE
CALGR
CALSP
CALFU
CALPU
CHRAU
CHRKA
CHRVE
COCST
COEBA
COEDI
COEFA
COEGE
COELI
COEPA
COEPO
COESI
COESP
COESD
Species
Byssoloma chlorinum (Vain.) Zahlbr.
Byssoloma leucoblepharum (Nyl.) Vain.
Byssoloma subdiscordans (Nyl.) P. James
Byssoloma subpolychromum Vezda
Calenia aspidota (Vain.) Vezda
Calenia bullatinoides Lücking
Calenia depressa Müll. Arg.
Calenia graphidea Vain.
Calenia sp.
Calopadia fusca (Müll. Arg.) Vezda
Calopadia puiggarii (Müll. Arg.) Vezda
Chroodiscus australiensis Vezda & Lumbsch
Chroodiscus kakamegensis sp. nov.
Chroodiscus verrucosus R. Sant., Lücking & Vezda
Coccocarpia stellata Tuck.
Coenogonium barbatum Lücking, Aptroot & Umaña
Coenogonium dilucidum (Kremp.) Kalb & Lücking
Coenogonium fallaciosum (Müll. Arg.) Kalb & Lücking
Coenogonium geralense (P.Henn) Lücking
Coenogonium lisowskii (Vezda) Lücking
Coenogonium pannosum Mull.Arg.
Coenogonium pocsii (Vezda & Farkas) Lücking
Coenogonium siquirrense (Lücking) Lücking
Coenogonium sp.
Coenogonium subdilucidum (Vezda) Lücking
Family
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Gomphillaceae
Gomphillaceae
Gomphillaceae
Gomphillaceae
Gomphillaceae
Pilocarpaceae
Pilocarpaceae
Thelotremataceae
Thelotremataceae
Thelotremataceae
Coccocarpiaceae
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Growth habit
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Facultative foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
208
Acronym
COESF
COESL
COEUS
COEZO
ECHDI
ECHPE
EUGWE
FELAF
FELBO
FELPA
FELRH
FELSF
FELSM
GYACA
GYAES
GYAFI
GYAFU
GYAIM
GYAMI
GYAEP
LICEP
LOFEP
LYRNE
MAZDI
MAZME
Species
Coenogonium subfallaciosum (Vezda & Farkas) Lücking
Coenogonium subluteum (Rehm) Kalb & Lücking
Coenogonium usambarense (Vezda & Farkas) Lücking & Kalb
Coenogonium zonatum (Müll. Arg.) Kalb & Lücking
Echinoplaca diffluens (Müll. Arg.) R. Sant.
Echinoplaca pellicula (Müll. Arg.) R. Sant.
Eugeniella wettsteinii (Müll.Arg.) Lücking, Sérus. & Kalb
Fellhanera africana (Vezda) Lücking
Fellhanera bouteillei (Desm.) Vezda
Fellhanera paradoxa (Vezda) Vezda
Fellhanera rhaphidophylli (Rehm) Vezda
Fellhanera subfuscatula Lücking
Fellhanera submicrommata (Vezda) Lücking & Kalb
Gyalectidium caucasicum (Elenk. & Woron.) Vezda
Gyalectidium eskuchei Sérus.
Gyalectidium filicinum Müll. Arg.
Gyalectidium fuscum Lücking & Sérus.
Gyalectidium imperfectum Vezda
Gyalectidium microcarpum (Vezda) Lücking, Sérus. & Vezda
Gyalidea epiphylla Vezda
Lichenopeltella epiphylla R. Sant.
Loflammia epiphylla (Fée) Lücking & Vezda
Lyromma nectandrae Bat. & H. Maia
Mazosia dispersa (Hedr.) R. Sant.
Mazosia melanopthalma (Müll. Arg.) R. Sant.
Family
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Gomphillaceae
Gomphillaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Gomphillaceae
Gomphillaceae
Gomphillaceae
Gomphillaceae
Gomphillaceae
Gomphillaceae
Asterothyriaceae
Microthyriaceae
Pilocarpaceae
Lyrommataceae
Roccellaceae
Roccellaceae
Growth habit
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Ubiquotus
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Lichenicolous fungi
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
209
Acronym
MAZPA
MAZPH
MAZRO
OPEEP
OPEMA
OPEPH
OPESP
PHYPO
PORAL
PORCF
PORCO
PORCU
POREP
POREI
PORKA
PORLE
PORLI
PORMA
PORNI
PORRA
PORRU
PORRB
PORRF
PORSE
PORSR
Species
Mazosia paupercula (Müll. Arg.) R. Sant.
Mazosia phyllosema (Nyl.) Zahlbr.
Mazosia rotula (Mont.) Massal.
Opegrapha epiporina Matzer
Opegrapha mazosiae Matzer
Opegrapha phylloporinae Müll. Arg.
Opegrapha sp.
Phylloblastia pocsii (Farkas & Vezda) Lücking
Porina alba (R.Sant.) Lücking
Porina cf. triseptata (Vezda) Lücking
Porina conica R. Sant.
Porina cupreola (Müll. Arg.) F. Schill. var. cupreola
Porina epiphylla (Fée) Fée
Porina epiphylloides Vezda
Porina kamerunensis F. Schill.
Porina leptosperma Müll. Arg.
Porina limbulata (Kremp.) Vain.
Porina mazosoides Lücking & Vezda
Porina nitidula Müll. Arg.
Porina radiata Kalb, Lücking & Vezda
Porina rubentior (Stirt.) Müll. Arg.
Porina rubescens (Lücking) Hafellner & Kalb
Porina rufula (Kremp.) Vain.
Porina semicarpi Vain.
Porina sphaerocephala Vain.
Family
Roccellaceae
Roccellaceae
Roccellaceae
Roccellaceae
Roccellaceae
Roccellaceae
Roccellaceae
Verrucariaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Growth habit
Typical foliicolous
Typical foliicolous
Typical foliicolous
Lichenicolous fungi
Lichenicolous fungi
Lichenicolous fungi
Lichenicolous fungi
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
210
Acronym
PORSH
PORSP
PORTE
PORTR
PSOPA
SPOAN
SPOLE
SPOPH
SPOPI
STRAN
STRJA
STRMA
STRMC
STRMI
STRMU
STRHY
STRNE
STRNI
STROB
STRPH
STRSC
STRSM
STRST
TAPMO
TAPNI
Species
Porina sphaerocephaloides Farkas
Porina subpallescensVezda
Porina tetramera (Malme) R. Sant.
Porina trichothelioides R. Sant.
Psorotheciopsis gyalideoides (Vezda) Henssen & Lücking
Sporopodium antonianum Elix, Lumbsch & Lücking
Sporopodium leprieurii Mont.
Sporopodium phyllocharis (Mont.) Massal.
Sporopodium pilocarpoides (Zahlbr.) Lücking & Kalb
Strigula antillarum (Fée) Müll. Arg.
Strigula janeriensis (Müll. Arg.) Lücking
Strigula macrocarpa Vain.
Strigula maculata (Cooke & Massee) R. Sant.
Strigula microspora Lücking
Strigula multipunctata (G. Merr. ex R. Sant.) R. C. Harris
Strigula nemathora var. hypothelia (Nyl.) R. Sant.
Strigula nemathora Mont.
Strigula nitidula Mont.
Strigula obducta (Müll. Arg.) R. C. Harris
Strigula phyllogena (Müll. Arg.) R. C. Harris
Strigula schizospora R. Sant.
Strigula smaragdula Fr.
Strigula subtilissima (Fée) Müll. Arg.
Tapellaria molleri (Lücking) Lücking
Tapellaria nigrata (Müll. Arg.) R. Sant.
Family
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Asterothyriaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Pilocarpaceae
Pilocarpaceae
Growth habit
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
211
Acronym
TRINI
TRIVA
TRIAF
TRIAL
TRIEP
TRISP
TRIPA
Species
Tricharia nigriuncinata sp.nov.
Tricharia vainioi R. Sant.
Trichothelium africanum Lücking
Trichothelium alboatrum Vain.
Trichothelium epiphyllum Müll. Arg.
Trichothelium minutum (Lücking) Lücking
Trichothelium pauciseptatum Vezda
Family
Gomphillaceae
Gomphillaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Growth habit
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
212
Appendix 7. Distribution of foliicolous lichens and lichenicolous fungi in the four forest
types of Budongo
Young
Old
secondary secondary
Primary
forest
Swamp
forest
Arthonia lividula
1
0
0
1
Arthonia orbygniae
0
1
0
0
Aspidothelium fugiens
1
1
0
0
Aspidothelium geminiparum
0
0
0
1
Asterothyrium microsporum
0
0
0
1
Asterothyrium monosporum
0
1
1
1
Asterothyrium pittieri
1
1
1
1
Asterothyrium rotuliforme
1
1
1
1
Asterothyrium septemseptatum ssp. africanum
0
1
0
1
Aulaxina microphana
0
1
1
1
Bacidina apiahica
1
1
1
1
Bacidina mirabilis
0
1
0
0
Bacidina pallidocarnea
0
1
0
0
Bacidina simplex
1
1
0
1
Bapalmuia ivoriensis
0
1
0
1
Bapalmuia palmularis
0
1
0
0
Brasilicia dimerelloides
1
1
1
1
Brasilicia foliicola
1
1
1
1
Byssolecania deplanata
1
1
1
1
Byssolecania fumosonigricans
1
1
1
1
Byssolecania hymenocarpa
1
1
1
1
Byssolecania variabilis
1
1
1
1
Byssoloma chlorinum
1
1
1
1
Byssoloma leucoblepharum
1
0
0
0
Byssoloma subdiscordans
0
0
0
1
Byssoloma subpolychromum
1
0
0
1
Calenia aspidota
1
1
1
1
Calenia bullatinoides
1
1
1
1
Calenia depressa
1
1
0
1
Calenia graphidea
1
0
1
1
Calenia sp.
0
0
0
1
Calopadia fusca
1
1
0
0
Calopadia puiggarii
0
1
0
1
Chroodiscus australiensis
1
0
1
1
Chroodiscus kakamegensis sp. nov.
0
0
0
1
Chroodiscus verrucosus
1
0
0
1
Coccocarpia stellata
1
1
1
1
Coenogonium barbatum
0
1
0
0
Coenogonium dilucidum
1
1
1
1
Species
213
Primary
forest
Swamp
forest
Coenogonium fallaciosum
0
0
0
1
Coenogonium geralense
1
1
1
1
Coenogonium lisowskii
0
1
1
1
Coenogonium pannosum
0
0
0
1
Coenogonium pocsii
1
1
1
1
Coenogonium siquirrense
1
1
1
1
Coenogonium sp.
0
1
0
1
Coenogonium subdilucidum
1
0
1
1
Coenogonium subfallaciosum
1
1
1
1
Coenogonium subluteum
1
1
1
1
Coenogonium usambarense
1
1
1
1
Coenogonium zonatum
1
1
0
1
Echinoplaca diffluens
1
1
1
1
Echinoplaca pellicula
1
0
0
1
Eugeniella wettsteinii
0
1
0
0
Fellhanera africana
0
1
0
1
Fellhanera bouteillei
0
1
0
1
Fellhanera paradoxa
1
1
1
1
Fellhanera rhaphidophylli
0
1
0
0
Fellhanera subfuscatula
1
1
1
1
Fellhanera submicrommata
1
1
1
1
Gyalectidium caucasicum
0
0
0
1
Gyalectidium eskuchei
0
0
0
1
Gyalectidium filicinum
1
1
1
1
Gyalectidium fuscum
0
1
0
0
Gyalectidium imperfectum
1
1
1
1
Gyalectidium microcarpum
0
0
0
1
Gyalidea epiphylla
1
1
1
1
Lichenopeltella epiphylla
0
0
1
1
Loflammia epiphylla
0
0
0
1
Lyromma nectandrae
1
1
1
1
Mazosia dispersa
1
0
0
0
Mazosia melanopthalma
1
1
1
1
Mazosia paupercula
0
1
0
0
Mazosia phyllosema
1
1
1
1
Mazosia rotula
1
1
1
0
Opegrapha epiporina
1
1
0
1
Opegrapha mazosiae
0
0
1
0
Opegrapha phylloporinae
1
1
0
0
Opegrapha sp.
0
0
1
1
Phylloblastia pocsii
0
1
0
1
Porina alba
1
1
1
1
Species
Old
Young
secondary secondary
214
Primary
forest
Swamp
forest
Porina cf. triseptata
1
0
0
1
Porina conica
1
1
1
0
Porina cupreola var. cupreola
1
1
0
1
Porina epiphylla
1
1
1
1
Porina epiphylloides
1
0
0
0
Porina kamerunensis
1
1
0
1
Porina leptosperma
1
1
0
1
Porina limbulata
1
1
1
1
Porina mazosoides
0
0
1
0
Porina nitidula
1
1
1
1
Porina radiata
1
1
1
1
Porina rubentior
1
1
1
0
Porina rubescens
1
1
1
0
Porina rufula
0
1
0
1
Porina semicarpi
1
1
0
1
Porina sphaerocephala
1
1
0
1
Porina sphaerocephaloides
1
0
0
0
Porina subpallescens
1
1
0
1
Porina tetramera
0
1
0
0
Porina trichothelioides
0
0
0
1
Psorotheciopsis patellarioides
1
1
1
1
Sporopodium antonianum
1
1
1
1
Sporopodium leprieurii
1
1
1
1
Sporopodium phyllocharis
0
1
1
1
Sporopodium pilocarpoides
0
0
0
1
Strigula antillarum
0
0
0
1
Strigula janeriensis
1
1
0
0
Strigula macrocarpa
1
1
1
1
Strigula maculata
0
0
0
1
Strigula microspora
1
1
1
1
Strigula multipunctata
1
1
0
1
Strigula nemathora var. hypothelia
1
1
1
1
Strigula nemathora
1
1
0
1
Strigula nitidula
0
0
0
2
Strigula obducta
0
1
0
1
Strigula phyllogena
1
1
0
0
Strigula schizospora
1
1
0
1
Strigula smaragdula
1
1
1
1
Strigula subtilissima
1
1
0
1
Tapellaria molleri
0
1
1
1
Tapellaria nigrata
0
1
0
0
Tricharia nigriuncinata sp.nov.
0
0
0
1
Species
Old
Young
secondary secondary
215
Primary
forest
Swamp
forest
Tricharia vainioi
1
0
0
1
Trichothelium africanum
1
1
0
0
Trichothelium alboatrum
0
1
0
0
Trichothelium epiphyllum
1
0
1
1
Trichothelium minutum
0
1
0
0
Trichothelium pauciseptatum
1
1
1
1
Species
Old
Young
secondary secondary
216
Appendix 8. Frequency of occurrence of species in the samples of Budongo
Forest
Species
Arthonia lividula
Arthonia orbygniae
Aspidothelium fugiens
Aspidothelium geminiparum
Asterothyrium microsporum
Asterothyrium monosporum
Asterothyrium pittieri
Asterothyrium rotuliforme
Asterothyrium septemseptatum ssp. africanum
Aulaxina microphana
Bacidina apiahica
Bacidina mirabilis
Bacidina pallidocarnea
Bacidina simplex
Bapalmuia ivoriensis
Bapalmuia palmularis
Brasilicia dimerelloides
Brasilicia foliicola
Byssolecania deplanata
Byssolecania fumosonigricans
Byssolecania hymenocarpa
Byssolecania variabilis
Byssoloma chlorinum
Byssoloma leucoblepharum
Byssoloma subdiscordans
Byssoloma subpolychromum
Calenia aspidota
Calenia bullatinoides
Calenia depressa
Calenia graphidea
Calenia sp.
Calopadia fusca
Calopadia puiggarii
Chroodiscus australiensis
Chroodiscus sp. nov.
Chroodiscus verrucosus
Coccocarpia stellata
Coenogonium barbatum
Coenogonium dilucidum
Frequency
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Occasional
Rare
Rare
Rare
Rare
Rare
Rare
Occasional
Occasional
Rare
Occasional
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Very frequent
217
Species
Coenogonium fallaciosum
Coenogonium geralense
Coenogonium lisowskii
Coenogonium pannosum
Coenogonium pocsii
Coenogonium siquirrense
Coenogonium sp.
Coenogonium subdilucidum
Coenogonium subfallaciosum
Coenogonium subluteum
Coenogonium usambarense
Coenogonium zonatum
Echinoplaca diffluens
Echinoplaca pellicula
Eugeniella wettsteinii
Fellhanera africana
Fellhanera bouteillei
Fellhanera paradoxa
Fellhanera rhaphidophylli
Fellhanera subfuscatula
Fellhanera submicrommata
Gyalectidium caucasicum
Gyalectidium eskuchei
Gyalectidium filicinum
Gyalectidium fuscum
Gyalectidium imperfectum
Gyalectidium microcarpum
Gyalidea epiphylla
Lichenopeltella epiphylla
Loflammia epiphylla
Lyromma nectandrae
Mazosia dispersa
Mazosia melanopthalma
Mazosia paupercula
Mazosia phyllosema
Mazosia rotula
Opegrapha epiporina
Opegrapha mazosiae
Opegrapha phylloporinae
Opegrapha sp.
Porina alba
Porina cf. triseptata
Frequency
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Occasional
Rare
Rare
Rare
Rare
Rare
Rare
Occasional
Rare
Rare
Occasional
Rare
Rare
Rare
Rare
Rare
Rare
Occasional
Rare
Frequent
Rare
Rare
Frequent
Rare
Rare
Rare
Rare
Less frequent
Rare
218
Species
Porina conica
Porina cupreola var. cupreola
Porina epiphylla
Porina epiphylloides
Porina kamerunensis
Porina leptosperma
Porina limbulata
Porina mazosoides
Porina nitidula
Porina radiata
Porina rubentior
Porina rubescens
Porina rufula
Porina semicarpi
Porina sphaerocephala
Porina sphaerocephaloides
Porina subpallescens
Porina tetramera
Porina trichothelioides
Psorotheciopsis patellarioides
Sporopodium antonianum
Sporopodium leprieurii
Sporopodium phyllocharis
Sporopodium pilocarpoides
Strigula antillarum
Strigula janeriensis
Strigula macrocarpa
Strigula maculata
Strigula microspora
Strigula multipunctata
Strigula nemathora var. hypothelia
Strigula nemathora
Strigula nitidula
Strigula obducta
Strigula phyllogena
Strigula schizospora
Strigula smaragdula
Strigula subtilissima
Tapellaria molleri
Tapellaria nigrata
Tricharia nigriuncinata sp.nov.
Tricharia vainioi
Frequency
Occasional
Occasional
Dominant
Occasional
Occasional
Occasional
Rare
Rare
Very frequent
Very frequent
Very frequent
Occasional
Rare
Less frequent
Less frequent
Rare
Rare
Rare
Rare
Rare
Rare
Occasional
Rare
Rare
Rare
Rare
Rare
Rare
Less frequent
Occasional
Frequent
Rare
Frequent
Occasional
Very frequent
Rare
Very frequent
Rare
Rare
Rare
Rare
Rare
219
Species
Trichothelium africanum
Trichothelium alboatrum
Trichothelium epiphyllum
Trichothelium minutum
Trichothelium pauciseptatum
Frequency
Rare
Rare
Rare
Rare
Rare
220
Appendix 9. Frequency of species in the samples of the primary forest type of Budongo
Species
Arthonia lividula
Aspidothelium fugiens
Asterothyrium microsporum
Asterothyrium monosporum
Bacidina apiahica
Bacidina mirabilis
Bacidina simplex
Bapalmuia ivoriensis
Bapalmuia palmularis
Brasilicia dimerelloides
Brasilicia foliicola
Byssolecania deplanata
Byssolecania fumosonigricans
Byssolecania hymenocarpa
Byssolecania variabilis
Byssoloma chlorinum
Byssoloma subpolychromum
Calenia bullatinoides
Calenia depressa
Calenia graphidea
Calopadia fusca
Chroodiscus australiensis
Chroodiscus kakamegensis sp. nov.
Chroodiscus verrucosus
Coenogonium dilucidum
Coenogonium fallaciosum
Coenogonium geralense
Coenogonium pannosum
Coenogonium pocsii
Coenogonium subdilucidum
Coenogonium subluteum
Coenogonium usambarense
Echinoplaca pellicula
Fellhanera bouteillei
Fellhanera submicrommata
Gyalectidium filicinum
Gyalectidium imperfectum
Gyalidea epiphylla
Lichenopeltella epiphylla
Lyromma nectandrae
Frequency
Rare
Rare
Rare
Rare
Rare
Occasional
Rare
Rare
Rare
Rare
Less frequent
Less frequent
Occasional
Occasional
Rare
Rare
Rare
Rare
Rare
Rare
Occasional
Rare
Rare
Rare
Dominant
Rare
Rare
Rare
Occasional
Rare
Occasional
Rare
Occasional
Rare
Rare
Rare
Rare
Rare
Rare
Occasional
221
Species
Mazosia dispersa
Mazosia melanopthalma
Mazosia phyllosema
Mazosia rotula
Phylloblastia pocsii
Porina alba
Porina cf. triseptata
Porina conica
Porina cupreola var. cupreola
Porina epiphylla
Porina epiphylloides
Porina kamerunensis
Porina leptosperma
Porina nitidula
Porina radiata
Porina rubentior
Porina rubescens
Porina rufula
Porina semicarpi
Porina sphaerocephala
Porina sphaerocephaloides
Porina subpallescens
Sporopodium antonianum
Sporopodium leprieurii
Sporopodium pilocarpoides
Strigula janeriensis
Strigula macrocarpa
Strigula microspora
Strigula multipunctata
Strigula nemathora var. hypothelia
Strigula nitidula
Strigula obducta
Strigula phyllogena
Strigula smaragdula
Strigula subtilissima
Tapellaria nigrata
Tricharia nigriuncinata sp.nov.
Tricharia vainioi
Trichothelium africanum
Trichothelium alboatrum
Trichothelium epiphyllum
Trichothelium pauciseptatum
Frequency
Rare
Dominant
Rare
Very frequent
Less frequent
Rare
Rare
Occasional
Dominant
Occasional
Occasional
Rare
Very frequent
Dominant
Occasional
Rare
Rare
Frequent
Less frequent
Rare
Rare
Rare
Occasional
Rare
Rare
Rare
Less frequent
Rare
Occasional
Less frequent
Rare
Very frequent
Less frequent
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
222
Appendix 10. Frequency of occurrence of species in the samples of the swamp
forest type of Budongo
Species
Arthonia orbygniae
Aspidothelium geminiparum
Asterothyrium microsporum
Asterothyrium monosporum
Bacidina apiahica
Bacidina mirabilis
Bacidina pallidocarnea
Bapalmuia ivoriensis
Bapalmuia palmularis
Brasilicia dimerelloides
Brasilicia foliicola
Byssolecania deplanata
Byssolecania fumosonigricans
Byssolecania hymenocarpa
Byssoloma chlorinum
Byssoloma leucoblepharum
Calenia aspidota
Calenia depressa
Calenia graphidea
Calopadia fusca
Calopadia puiggarii
Chroodiscus australiensis
Chroodiscus verrucosus
Coenogonium barbatum
Coenogonium dilucidum
Coenogonium fallaciosum
Coenogonium geralense
Coenogonium lisowskii
Coenogonium pocsii
Coenogonium siquirrense
Coenogonium sp.
Coenogonium subdilucidum
Coenogonium subfallaciosum
Coenogonium subluteum
Coenogonium usambarense
Coenogonium zonatum
Echinoplaca pellicula
Fellhanera africana
Fellhanera rhaphidophylli
Fellhanera subfuscatula
Fellhanera submicrommata
Gyalectidium caucasicum
Frequency
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Occasional
Occasional
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Dominant
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
223
Species
Gyalectidium eskuchei
Gyalectidium filicinum
Gyalectidium imperfectum
Gyalidea epiphylla
Lichenopeltella epiphylla
Loflammia epiphylla
Lyromma nectandrae
Mazosia dispersa
Mazosia melanopthalma
Mazosia paupercula
Mazosia phyllosema
Mazosia rotula
Opegrapha epiporina
Opegrapha phylloporinae
Porina alba
Porina conica
Porina epiphylla
Porina epiphylloides
Porina leptosperma
Porina mazosoides
Porina nitidula
Porina radiata
Porina rubentior
Porina rubescens
Porina rufula
Porina semicarpi
Porina sphaerocephala
Porina sphaerocephaloides
Porina subpallescens
Psorotheciopsis patellarioides
Sporopodium antonianum
Sporopodium leprieurii
Sporopodium phyllocharis
Sporopodium pilocarpoides
Strigula antillarum
Strigula janeriensis
Strigula macrocarpa
Strigula maculata
Strigula microspora
Strigula multipunctata
Strigula nemathora var. hypothelia
Strigula nemathora
Strigula nitidula
Strigula obducta
Strigula phyllogena
Frequency
Rare
Occasional
Rare
Rare
Rare
Rare
Occasional
Rare
Frequent
Rare
Rare
Very frequent
Rare
Rare
Very frequent
Less frequent
Dominant
Occasional
Occasional
Rare
Very frequent
Very frequent
Very frequent
Occasional
Occasional
Frequent
Frequent
Rare
Rare
Rare
Rare
Less frequent
Rare
Rare
Rare
Rare
Rare
Rare
Less frequent
Rare
Less frequent
Occasional
Frequent
Less frequent
Dominant
224
Species
Strigula schizospora
Strigula smaragdula
Strigula subtilissima
Tricharia nigriuncinata sp.nov.
Tricharia vainioi
Trichothelium africanum
Trichothelium alboatrum
Trichothelium epiphyllum
Trichothelium pauciseptatum
Frequency
Rare
Frequent
Rare
Rare
Occasional
Rare
Rare
Rare
Occasional
225
Appendix 11. Frequency of occurrence of species in the samples of the old
secondary forest type of Budongo
Species
Arthonia lividula
Asterothyrium microsporum
Bacidina apiahica
Bacidina mirabilis
Bacidina simplex
Brasilicia dimerelloides
Brasilicia foliicola
Byssolecania deplanata
Byssolecania fumosonigricans
Byssolecania hymenocarpa
Byssoloma chlorinum
Byssoloma subdiscordans
Coenogonium dilucidum
Coenogonium geralense
Coenogonium pocsii
Coenogonium siquirrense
Coenogonium subluteum
Coenogonium usambarense
Coenogonium zonatum
Fellhanera submicrommata
Gyalectidium filicinum
Gyalectidium imperfectum
Lichenopeltella epiphylla
Lyromma nectandrae
Biatora sp.
Mazosia melanopthalma
Mazosia phyllosema
Mazosia rotula
Opegrapha epiporina
Opegrapha mazosiae
Opegrapha phylloporinae
Opegrapha sp.
Porina alba
Porina conica
Porina cupreola var. cupreola
Porina epiphylla
Porina kamerunensis
Porina leptosperma
Porina nitidula
Porina radiata
Porina rubentior
Frequency
Rare
Rare
Less frequent
Rare
Rare
Rare
Occasional
Rare
Rare
Less frequent
Occasional
Rare
Occasional
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Occasional
Rare
Dominant
Rare
Rare
Occasional
Rare
Occasional
Occasional
Rare
Rare
Very frequent
Dominant
Dominant
Rare
Dominant
Frequent
Dominant
226
Species
Porina rubescens
Porina rufula
Porina semicarpi
Porina sphaerocephala
Porina subpallescens
Strigula janeriensis
Strigula macrocarpa
Strigula microspora
Strigula multipunctata
Strigula nemathora var. hypothelia
Strigula nemathora
Strigula nitidula
Strigula obducta
Strigula phyllogena
Strigula schizospora
Strigula smaragdula
Strigula subtilissima
Trichothelium africanum
Trichothelium epiphyllum
Trichothelium pauciseptatum
Frequency
Frequent
Less frequent
Occasional
Frequent
Rare
Rare
Rare
Less frequent
Less frequent
Frequent
Rare
Very frequent
Rare
Dominant
Rare
Frequent
Rare
Rare
Rare
Rare
227
Appendix 12 Frequency of species in the samples of the young secondary forest
type of Budongo
Species
Arthonia lividula
Aspidothelium fugiens
Asterothyrium microsporum
Asterothyrium pittieri
Asterothyrium rotuliforme
Asterothyrium septemseptatum ssp. africanum
Aulaxina microphana
Bacidina apiahica
Bacidina simplex
Biatora sp.
Brasilicia dimerelloides
Brasilicia foliicola
Byssolecania deplanata
Byssolecania fumosonigricans
Byssolecania hymenocarpa
Byssolecania variabilis
Byssoloma chlorinum
Byssoloma leucoblepharum
Byssoloma subpolychromum
Calenia aspidota
Calenia bullatinoides
Calenia depressa
Calenia graphidea
Calenia sp.
Calopadia fusca
Calopadia puiggarii
Chroodiscus australiensis
Chroodiscus verrucosus
Coccocarpia stellata
Coenogonium dilucidum
Coenogonium geralense
Coenogonium lisowskii
Coenogonium pocsii
Coenogonium siquirrense
Coenogonium sp.
Coenogonium subdilucidum
Coenogonium subfallaciosum
Frequency
Rare
Rare
Rare
Rare
Rare
Rare
Rare
Occasional
Rare
Rare
Rare
Rare
Occasional
Rare
Occasional
Rare
Occasional
Rare
Rare
Rare
Rare
Occasional
Occasional
Rare
Rare
Rare
Rare
Rare
Rare
Frequent
Rare
Rare
Rare
Rare
Rare
Rare
Rare
228
Species
Coenogonium subluteum
Coenogonium usambarense
Coenogonium zonatum
Echinoplaca diffluens
Echinoplaca pellicula
Eugeniella wettsteinii
Fellhanera bouteillei
Fellhanera paradoxa
Fellhanera subfuscatula
Fellhanera submicrommata
Gyalectidium filicinum
Gyalectidium fuscum
Gyalectidium imperfectum
Gyalectidium microcarpum
Gyalidea epiphylla
Lyromma nectandrae
Mazosia dispersa
Mazosia melanopthalma
Mazosia phyllosema
Mazosia rotula
Opegrapha epiporina
Opegrapha phylloporinae
Opegrapha sp.
Porina alba
Porina cf. triseptata
Porina conica
Porina cupreola var. cupreola
Porina epiphylla
Porina epiphylloides
Porina kamerunensis
Porina leptosperma
Porina limbulata
Porina nitidula
Porina radiata
Porina rubentior
Porina rubescens
Porina semicarpi
Porina sphaerocephala
Porina sphaerocephaloides
Porina subpallescens
Porina tetramera
Porina trichothelioides
Frequency
Rare
Rare
Rare
Rare
Less frequent
Rare
Rare
Rare
Rare
Occasional
Occasional
Rare
Occasional
Occasional
Rare
Occasional
Rare
Occasional
Rare
Frequent
Rare
Rare
Rare
Rare
Rare
Rare
Occasional
Frequent
Occasional
Occasional
Occasional
Rare
Very frequent
Less frequent
Very frequent
Occasional
Rare
Less frequent
Occasional
Occasional
Rare
Rare
229
Species
Psorotheciopsis patellarioides
Sporopodium antonianum
Sporopodium leprieurii
Strigula antillarum
Strigula janeriensis
Strigula macrocarpa
Strigula microspora
Strigula multipunctata
Strigula nemathora var. hypothelia
Strigula nemathora
Strigula nitidula
Strigula phyllogena
Strigula schizospora
Strigula smaragdula
Strigula subtilissima
Tapellaria molleri
Tricharia vainioi
Trichothelium africanum
Trichothelium epiphyllum
Trichothelium minutum
Trichothelium pauciseptatum
Frequency
Rare
Rare
Rare
Rare
Rare
Rare
Less frequent
Occasional
Very frequent
Rare
Very frequent
Frequent
Rare
Dominant
Rare
Rare
Rare
Rare
Rare
Rare
Rare
230
Appendix 13 Foliicolous lichens and lichenicolous fungi from Kakamega Forest
Acronym Species
Aderkomyces dilatatus (Vezda) Lücking, Serusiaux & Vezda
Arthonia atropunctata Vain.
Arthonia flavoverrucosa U. Becker & Lücking
Arthonia fuscocyanea U. Becker & Lücking
Arthonia lividula Vain.
Arthonia orbygniae (H. B. P. Upadhyay) Matzer
Aspidothelium fugiens (Müll. Arg.) R. Sant.
Aspidothelium geminiparum (Malme) R. Sant.
Aspidothelium hirustum sp. nov.
Aspidothelium scutelicarpum Lücking
Asterothyrium aulaxinoides Lücking
Asterothyrium leucophthalmum (Müll. Arg.) R. Sant.
Asterothyrium microsporum R. Sant.
Asterothyrium pittieri Müll. Arg.
Asterothyrium rotuliforme (Müll. Arg.) Sérus.
Asterothyrium septemseptatum ssp. africanum Lücking & Kalb
Asterothyrium sp.
Aulaxina epiphylla (Zahlbr.) R. Sant.
Aulaxina opegraphina Fée
Bacidia medialis (Tuck. ex Nyl.) de Lesd.
Bacidina apiahica (Müll. Arg.) Vezda
Bacidina mirabilis (Vezda) Vezda
Bacidina pallidocarnea (Müll. Arg.) Vezda
Bacidina simplex Farkas & Vezda
Badimia dimidiata (C. Bab. ex Leight.) Vezda
Bapalmuia ivoriensis R. Sant. & Lücking
Family
Gomphillaceae
Arthoniaceae
Arthoniaceae
Arthoniaceae
Arthoniaceae
Arthoniaceae
Aspidotheliaceae
Aspidotheliaceae
Aspidotheliaceae
Aspidotheliaceae
Asterothyriaceae
Asterothyriaceae
Asterothyriaceae
Asterothyriaceae
Asterothyriaceae
Asterothyriaceae
Asterothyriaceae
Gomphillaceae
Gomphillaceae
Ramalinaceae
Ramalinaceae
Ramalinaceae
Ramalinaceae
Ramalinaceae
Pilocarpaceae
Pilocarpaceae
Growth habit
Typical foliicolous
Lichenicolous fungi
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Facultative foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
231
Acronym Species
Biatora sp.
Brasilicia dimerelloides (Vezda) Lücking, Kalb & Sérus.
Brasilicia foliicola (Vezda) Lücking, Kalb & Sérus.
Byssolecania deplanata (Müll. Arg.) R. Sant.
Byssolecania hymenocarpa (Vain.) Kalb, Vezda & Lücking
Byssolecania variabilis (Vain.) Kalb, Vezda & Lücking
Byssoloma chlorinum (Vain.) Zahlbr.
Byssoloma leucoblepharum (Nyl.) Vain.
Byssoloma subdiscordans (Nyl.) P. James
Calenia aspidota (Vain.) Vezda
Calenia bullatinoides Lücking
Calenia depressa Müll. Arg.
Calenia graphidea Vain.
Calenia monospora Vezda
Calenia sp.
Calenia thelotremela Vain.
Calopadia fusca (Müll. Arg.) Vezda
Calopadia puiggarii (Müll. Arg.) Vezda
Calopadia subcoerulescens (Zahlbr.) Vezda
Chroodiscus australiensis Vezda & Lumbsch
Chroodiscus kakamegensis sp. nov.
Chroodiscus verrucosus R. Sant., Lücking & Vezda
Coccocarpia stellata Tuck.
Coenogonium dilucidum (Kremp.) Kalb & Lücking
Coenogonium fallaciosum (Müll. Arg.) Kalb & Lücking
Coenogonium flavum (Malcom & Vezda) Lücking
Coenogonium geralense (P.Henn) Lücking
Coenogonium lisowskii (Vezda) Lücking
Family
Bacidiaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Gomphillaceae
Gomphillaceae
Gomphillaceae
Gomphillaceae
Gomphillaceae
Gomphillaceae
Gomphillaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Thelotremataceae
Thelotremataceae
Thelotremataceae
Coccocarpiaceae
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Growth habit
Facultative foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Facultative foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
232
Acronym Species
Coenogonium pocsii (Vezda & Farkas) Lücking
Coenogonium siquirrense (Lücking) Lücking
Coenogonium sp.
Coenogonium subdilucidum (Vezda) Lücking
Coenogonium subfallaciosum (Vezda & Farkas) Lücking
Coenogonium subluteum (Rehm) Kalb & Lücking
Coenogonium usambarense (Vezda & Farkas) Lücking & Kalb
Coenogonium zonatum (Müll. Arg.) Kalb & Lücking
Echinoplaca diffluens (Müll. Arg.) R. Sant.
Echinoplaca pellicula (Müll. Arg.) R. Sant.
Enterographa fellhaneroides sp.nov.
Enterographa meklitiae sp.nov.
Eremothecella calamicola Syd.
Fellhanera bouteillei (Desm.) Vezda
Fellhanera aff. bouteillei
Fellhanera encephalarti (Vezda) Vezda
Fellhanera paradoxa (Vezda) Vezda
Fellhanera parvula (Vezda) Vezda
Fellhanera rhaphidophylli (Rehm) Vezda
Fellhanera subfuscatula Lücking
Fellhanera sublecanorina (Nyl.) Vezda
Fellhanera submicrommata (Vezda) Lücking & Kalb
Gyalectidium caucasicum (Elenk. & Woron.) Vezda
Gyalectidium eskuchei Sérus.
Gyalectidium filicinum Müll. Arg.
Gyalectidium fuscum Lücking & Sérus.
Gyalectidium imperfectum Vezda
Gyalidea epiphylla Vezda
Family
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Coenogoniaceae
Gomphillaceae
Gomphillaceae
Roccellaceae
Roccellaceae
Arthoniaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Gomphillaceae
Gomphillaceae
Gomphillaceae
Gomphillaceae
Gomphillaceae
Asterothyriaceae
Growth habit
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Ubiquotus
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
233
Acronym Species
Gyalidea psorotheciopides sp. nov.
Gyalideopsis cochlearifer Lücking & Sérus.
Lasioloma arachnoideum (Kremp.) R. Sant.
Lichenopeltella epiphylla R. Sant.
Loflammia epiphylla (Fée) Lücking & Vezda
Lyromma nectandrae Bat. & H. Maia
Mazosia melanopthalma (Müll. Arg.) R. Sant.
Musaespora kalbii Lücking & Sérus.
Opegrapha epiporina Matzer
Opegrapha phylloporinae Müll. Arg.
Opegrapha sp.
Opegrapha velata (Müll. Arg.) Vain.
Phylloblastia pocsii (Farkas & Vezda) Lücking
Phyllospora sp.
Porina atrocoerulea Müll. Arg.
Porina cf. triseptata (Vezda) Lücking
Porina cupreola (Müll. Arg.) F. Schill. var. cupreola
Porina distans Vezda & Vivant
Porina epiphylla (Fée) Fée
Porina epiphylloides Vezda
Porina kamerunensis F. Schill.
Porina leptosperma Müll. Arg.
Porina limbulata (Kremp.) Vain.
Porina lucida R. Sant. var. lucida
Porina mazosoides Lücking & Vezda
Porina nitidula Müll. Arg.
Porina pallescens R. Sant.
Porina rubentior (Stirt.) Müll. Arg.
Family
Asterothyriaceae
Gomphillaceae
Pilocarpaceae
Microthyriaceae
Pilocarpaceae
Lyrommataceae
Roccellaceae
Monoblastiaceae
Roccellaceae
Roccellaceae
Roccellaceae
Roccellaceae
Verrucariaceae
Bacidiaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Growth habit
Typical foliicolous
Lichenicolous fungi
Typical foliicolous
Lichenicolous fungi
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Lichenicolous fungi
Lichenicolous fungi
Lichenicolous fungi
Lichenicolous fungi
Typical foliicolous
Facultative foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
234
Acronym Species
Porina rubescens (Lücking) Hafellner & Kalb
Porina rufula (Kremp.) Vain.
Porina semicarpi Vain.
Porina sphaerocephaloides Farkas
Porina subpallescensVezda
Porina tetramera (Malme) R. Sant.
Porina trichothelioides R. Sant.
Psorotheciopsis gyalideoides (Vezda) Henssen & Lücking
Psorotheciopsis patellarioides (Rehm) R. Sant.
Psorotheciopsis varieseptata (Vezda) Henssen & Lücking
Sporopodium antonianum Elix, Lumbsch & Lücking
Sporopodium leprieurii Mont.
Sporopodium pilocarpoides (Zahlbr.) Lücking & Kalb
Sporopodium sp.
Strigula antillarum (Fée) Müll. Arg.
Strigula concreta (Fée) R. Sant.
Strigula janeriensis (Müll. Arg.) Lücking
Strigula macrocarpa Vain.
Strigula maculata (Cooke & Massee) R. Sant.
Strigula melanobapha (Kremp.) R. Sant.
Strigula microspora Lücking
Strigula nemathora var. hypothelia (Nyl.) R. Sant.
Strigula nemathora Mont.
Strigula nitidula Mont.
Strigula obducta (Müll. Arg.) R. C. Harris
Strigula phyllogena (Müll. Arg.) R. C. Harris
Strigula schizospora R. Sant.
Strigula smaragdula Fr.
Family
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Asterothyriaceae
Asterothyriaceae
Asterothyriaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Pilocarpaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Strigulaceae
Growth habit
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
235
Acronym Species
Strigula subtilissima (Fée) Müll. Arg.
Tapellaria epiphylla (Müll. Arg.) R. Sant.
Tapellaria nigrata (Müll. Arg.) R. Sant.
Tricharia vainioi R. Sant.
Trichothelium africanum Lücking
Trichothelium epiphyllum Müll. Arg.
Trichothelium minutum (Lücking) Lücking
Trichothelium pauciseptatum Vezda
Family
Strigulaceae
Pilocarpaceae
Pilocarpaceae
Gomphillaceae
Porinaceae
Porinaceae
Porinaceae
Porinaceae
Growth habit
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
Typical foliicolous
236
Appendix 14 Distribution of foliicolous lichens and lichenicolous fungi in the various forest sites of Kakamega Forest.
Camp site
Colobus
Ghostisland
Ikuywa
Isecheno
Isikuhu
Kaimosi
Kisere
Malava
Salazar
Yala
0
0
0
0
0
0
0
0
1
0
0
0
0
0
Arthonia atropunctata
0
0
0
0
0
0
0
0
0
0
1
0
0
0
Arthonia flavoverrucosa
0
1
0
0
0
0
0
0
0
0
0
0
0
0
Arthonia fuscocyanea
0
1
0
0
0
0
0
0
0
0
0
0
0
0
Arthonia lividula
0
0
1
0
0
0
1
1
1
0
0
1
0
1
Arthonia orbygniae
0
0
0
0
0
0
0
0
1
0
0
0
0
1
Aspidothelium fugiens
0
1
0
0
0
0
1
0
1
0
0
0
1
1
Aspidothelium geminiparum
0
0
0
0
0
0
0
0
1
0
0
0
0
0
Aspidothelium scutelicarpum
0
0
0
0
0
0
0
0
1
0
0
0
0
0
Aspidothelium hirsutum sp. nov.
0
0
0
0
0
0
0
0
0
0
1
0
0
0
Asterothyrium aulaxinoides
0
0
1
1
0
0
0
0
0
0
0
0
0
0
Asterothyrium leucophthalmum
0
0
1
1
0
0
0
0
0
0
0
0
0
0
Asterothyrium microsporum
0
0
1
0
0
0
0
0
1
0
1
1
1
0
Asterothyrium pittieri
0
0
1
1
0
0
0
0
0
0
0
0
0
0
Asterothyrium rotuliforme
0
1
0
1
0
1
0
0
0
1
1
1
0
0
Asterothyrium septemseptatum ssp. africanum
0
0
0
1
0
0
0
0
0
0
0
0
0
0
Asterothyrium sp.
0
0
0
1
0
0
0
0
0
0
0
0
0
0
Aulaxina epiphylla
0
1
0
1
0
0
1
0
1
0
0
0
0
1
Aulaxina opegraphina
0
0
0
0
0
0
0
0
1
0
0
0
0
0
Bacidia medialis
0
0
0
0
0
0
0
0
0
0
0
1
0
0
Bacidina apiahica
1
1
1
1
1
1
1
0
0
1
1
1
1
0
Busambuli
Aderkomyces dilatatus
Buyangu
Species
Bukhaywa
1 = present, 0 = absent
237
Camp site
Colobus
Ghostisland
Ikuywa
Isecheno
Isikuhu
Kaimosi
Kisere
Malava
Salazar
Yala
0
1
0
0
0
0
1
0
0
0
1
0
1
0
Bacidina pallidocarnea
1
0
1
0
0
0
0
0
0
0
1
1
0
0
Bacidina simplex
1
1
0
0
1
0
1
1
1
0
1
1
1
0
Badimia dimidiata
0
1
0
0
0
0
0
0
1
0
0
0
0
0
Bapalmuia ivoriensis
0
0
0
0
0
0
0
0
0
0
0
0
1
1
Biatora sp.
0
0
0
0
0
0
0
1
0
0
1
1
0
1
Brasilicia dimerelloides
1
1
0
0
0
0
1
0
0
0
0
0
1
1
Brasilicia foliicola
0
0
0
0
0
0
1
1
1
1
1
0
1
1
Byssolecania deplanata
0
0
0
0
0
0
1
0
0
0
1
0
0
1
Byssolecania hymenocarpa
0
0
0
0
0
0
0
0
0
0
1
0
0
0
Byssolecania variabilis
0
0
0
0
0
0
1
0
0
0
1
0
0
1
Byssoloma chlorinum
1
0
1
0
1
0
1
0
1
0
1
1
0
1
Byssoloma leucoblepharum
1
1
1
0
1
1
1
1
1
0
1
1
1
1
Byssoloma subdiscordans
0
1
0
0
0
0
0
0
1
0
0
0
0
0
Calenia aspidota
0
1
1
1
0
1
1
1
1
1
1
0
1
1
Calenia bullatinoides
0
1
0
0
1
0
0
0
0
0
0
0
1
0
Calenia depressa
1
1
1
1
0
0
1
0
1
0
0
0
1
1
Calenia graphidea
0
1
1
0
0
0
1
0
1
0
1
0
1
1
Calenia monospora
1
1
1
1
1
1
1
1
1
1
1
1
1
1
Calenia sp.
0
0
0
0
0
0
0
0
1
0
0
0
0
0
Calenia thelotremela
0
0
0
0
0
0
0
0
1
0
0
0
0
0
Calopadia fusca
1
1
1
0
1
1
1
1
1
1
1
1
1
1
Calopadia puiggarii
1
1
1
0
1
1
1
1
1
1
1
1
1
1
Calopadia subcoerulescens
0
0
1
0
0
0
1
1
1
1
0
0
1
1
Chroodiscus australiensis
0
0
0
0
0
0
1
0
0
0
0
0
0
0
Busambuli
Bukhaywa
Bacidina mirabilis
Buyangu
Species
238
Camp site
Colobus
Ghostisland
Ikuywa
Isecheno
Isikuhu
Kaimosi
Kisere
Malava
Salazar
Yala
0
1
0
0
0
1
0
1
0
1
1
1
1
0
Chroodiscus verrucosus
0
1
1
1
0
1
1
1
1
0
1
1
1
1
Coccocarpia stellata
0
0
1
0
0
0
0
0
0
1
0
1
0
0
Coenogonium dilucidum
0
1
0
0
0
0
1
0
1
0
1
0
1
1
Coenogonium fallaciosum
0
1
0
0
0
0
0
0
0
0
0
0
1
0
Coenogonium flavum
1
0
1
0
1
0
0
1
0
0
1
0
0
0
Coenogonium geralense
1
1
1
0
1
1
1
1
1
0
1
1
1
1
Coenogonium lisowskii
1
0
1
0
1
0
1
1
1
0
1
1
1
1
Coenogonium pocsii
0
1
0
0
1
0
1
1
1
0
1
0
1
1
Coenogonium siquirrense
0
0
0
0
1
0
1
1
0
1
1
0
1
1
Coenogonium sp.
1
1
0
0
1
1
0
1
0
0
1
1
1
1
Coenogonium subdilucidum
0
0
0
0
1
0
0
0
1
0
0
0
1
1
Coenogonium subfallaciosum
0
1
0
0
0
1
0
1
1
0
1
0
1
1
Coenogonium subluteum
0
1
1
0
1
0
1
0
1
1
1
0
1
1
Coenogonium usambarense
0
1
0
0
0
0
1
0
0
1
1
0
1
1
Coenogonium zonatum
0
1
0
0
1
1
0
0
0
1
1
0
1
1
Echinoplaca diffluens
0
0
0
0
0
0
0
0
0
0
0
0
1
1
Echinoplaca pellicula
0
0
0
0
0
0
1
0
0
0
0
0
1
1
Enterographa fellhaneroides sp.nov.
0
0
0
0
0
0
0
1
0
0
1
0
0
0
Enterographa meklitiae sp.nov.
0
0
1
0
1
0
1
1
0
0
1
0
0
0
Eremothecella calamicola
0
0
0
0
0
0
0
0
1
0
0
0
0
0
Fellhanera bouteillei
1
1
1
1
0
0
1
0
1
1
1
1
0
1
Fellhanera aff. bouteillei
0
0
0
0
0
0
1
0
0
0
1
0
0
1
Fellhanera encephalarti
0
0
0
0
0
0
1
0
0
0
0
0
0
0
Fellhanera paradoxa
0
0
0
0
0
0
1
0
0
0
0
0
0
1
Busambuli
Bukhaywa
Chroodiscus kakamegensis sp. nov.
Buyangu
Species
239
Camp site
Colobus
Ghostisland
Ikuywa
Isecheno
Isikuhu
Kaimosi
Kisere
Malava
Salazar
Yala
0
0
1
0
0
0
0
0
0
0
0
0
0
0
Fellhanera rhaphidophylli
0
0
0
0
0
0
0
0
0
0
1
0
0
1
Fellhanera subfuscatula
0
1
1
0
0
0
0
0
1
0
1
0
1
1
Fellhanera sublecanorina
0
0
1
0
0
0
0
0
0
1
0
0
0
0
Fellhanera submicrommata
0
0
1
0
0
0
0
0
0
1
1
0
0
0
Gyalectidium caucasicum
1
1
1
0
0
0
1
1
1
0
1
0
1
1
Gyalectidium eskuchei
0
0
0
1
0
1
0
0
0
0
0
0
0
0
Gyalectidium filicinum
1
1
1
1
1
1
1
1
1
1
1
1
1
1
Gyalectidium fuscum
0
1
0
1
0
0
0
0
0
0
1
1
0
0
Gyalectidium imperfectum
0
0
0
1
0
0
1
0
1
1
0
1
0
0
Gyalidea epiphylla
1
0
0
0
1
0
0
1
1
0
1
0
1
1
Gyalidea psorotheciopides sp. nov.
1
1
0
0
0
0
0
0
0
0
0
1
0
0
Gyalideopsis cochlearifer
0
0
0
0
0
0
0
0
1
0
0
0
0
0
Lasioloma arachnoideum
0
1
0
0
0
0
0
0
1
0
0
0
0
0
Lichenopeltella epiphylla
0
0
0
0
0
0
0
0
0
0
0
0
1
0
Loflammia epiphylla
0
0
0
0
0
0
0
0
1
0
1
0
0
0
Lyromma nectandrae
1
1
0
0
1
1
1
1
1
1
1
0
1
1
Mazosia melanopthalma
1
1
0
0
1
0
1
0
1
0
1
0
1
1
Musaespora kalbii
0
1
0
0
0
0
0
0
0
0
0
0
0
0
Opegrapha epiporina
1
1
0
0
0
0
0
0
1
1
0
0
1
0
Opegrapha phylloporinae
1
1
1
0
1
0
1
1
1
1
1
1
0
1
Opegrapha sp.
1
0
1
0
0
0
0
0
0
0
0
1
0
0
Opegrapha velata
1
0
1
0
1
0
0
0
1
1
1
0
0
0
Phylloblastia pocsii
1
0
0
0
1
0
0
1
0
0
1
0
1
0
Phyllospora sp.
1
0
0
0
0
0
0
0
1
0
1
0
0
0
Busambuli
Bukhaywa
Fellhanera parvula
Buyangu
Species
240
Camp site
Colobus
Ghostisland
Ikuywa
Isecheno
Isikuhu
Kaimosi
Kisere
Malava
Salazar
Yala
1
0
0
0
0
0
0
0
0
0
1
1
1
1
Porina atrocoerulea
0
0
0
0
0
0
0
0
1
0
0
0
0
0
Porina cupreola var. cupreola
1
1
1
0
1
1
1
1
1
1
1
1
1
1
Porina distans
1
0
0
0
0
0
0
1
0
1
0
0
0
0
Porina epiphylla
1
1
1
1
1
1
1
1
1
1
1
1
1
1
Porina epiphylloides
0
1
1
0
0
0
0
1
1
0
1
0
1
1
Porina kamerunensis
0
0
0
0
1
0
0
0
0
0
0
0
0
0
Porina leptosperma
0
1
0
0
0
0
0
0
0
0
0
0
1
1
Porina limbulata
0
1
0
0
1
0
0
0
1
0
1
0
0
0
Porina lucida var. lucida
0
1
0
0
0
0
0
0
0
0
0
0
0
0
Porina mazosoides
0
1
0
0
0
0
0
0
1
0
0
0
1
0
Porina nitidula
1
1
1
1
1
1
1
1
1
1
1
1
1
1
Porina pallescens
0
0
0
0
0
0
0
0
0
0
0
0
1
0
Porina rubentior
1
1
1
1
1
1
1
1
1
1
1
1
1
1
Porina rubescens
0
0
0
0
1
1
1
1
0
1
1
1
1
1
Porina rufula
0
1
0
0
0
0
0
1
0
1
0
1
1
0
Porina semicarpi
0
1
0
0
0
1
1
1
1
0
0
0
1
1
Porina sphaerocephaloides
0
1
0
0
0
0
0
0
1
0
0
0
0
0
Porina subpallescens
1
1
1
0
1
1
1
1
1
1
1
1
1
1
Porina tetramera
1
0
0
0
0
0
0
0
0
0
0
0
1
1
Porina trichothelioides
0
0
0
0
1
0
0
0
1
0
0
0
0
0
Psorotheciopsis gyalideoides
0
0
0
1
0
0
0
0
0
0
0
0
0
0
Psorotheciopsis patellarioides
1
0
0
1
1
1
1
0
0
0
1
1
0
0
Psorotheciopsis varieseptata
0
1
1
1
0
0
0
0
0
0
1
1
0
0
Sporopodium antonianum
0
1
0
0
0
0
1
0
0
1
0
0
1
1
Busambuli
Bukhaywa
Porina cf. triseptata
Buyangu
Species
241
Camp site
Colobus
Ghostisland
Ikuywa
Isecheno
Isikuhu
Kaimosi
Kisere
Malava
Salazar
Yala
0
1
0
0
0
0
0
0
1
0
0
0
0
1
Sporopodium pilocarpoides
0
1
0
0
0
0
1
0
1
0
1
0
1
1
Sporopodium sp.
0
0
0
0
0
0
0
0
1
0
1
0
0
0
Strigula antillarum
1
1
1
0
0
0
0
1
1
0
0
0
0
0
Strigula concreta
0
0
1
0
0
0
0
0
0
0
0
0
0
1
Strigula janeriensis
0
0
0
0
0
0
1
0
0
0
0
0
0
0
Strigula macrocarpa
1
1
1
0
1
1
1
1
1
0
1
1
1
1
Strigula maculata
0
1
0
0
0
0
0
0
1
0
0
0
0
0
Strigula melanobapha
0
1
0
0
0
0
0
0
1
0
0
0
0
0
Strigula microspora
1
1
1
1
1
1
1
1
1
0
1
1
1
1
Strigula nemathora var. hypothelia
1
1
1
0
0
0
1
1
0
1
1
1
1
1
Strigula nemathora
1
0
0
0
0
0
0
0
1
0
1
0
0
0
Strigula nitidula
1
1
1
1
1
0
1
1
1
1
1
1
1
1
Strigula obducta
1
1
1
0
1
0
1
1
1
0
1
1
1
1
Strigula phyllogena
1
1
1
0
1
1
1
1
1
1
1
1
1
1
Strigula schizospora
0
1
1
0
1
1
1
1
1
1
1
1
1
1
Strigula smaragdula
1
1
1
1
1
1
1
1
1
1
1
1
1
1
Strigula subtilissima
0
0
0
0
0
0
0
1
0
1
1
0
1
1
Tapellaria epiphylla
0
0
1
0
0
0
0
0
1
0
0
0
0
0
Tapellaria nigrata
0
0
0
0
0
0
0
0
0
0
1
0
0
0
Tricharia vainioi
0
1
1
0
0
0
1
0
1
1
0
0
1
1
Trichothelium africanum
0
1
1
0
1
1
1
0
1
1
0
0
0
0
Trichothelium epiphyllum
1
1
0
0
1
0
0
0
1
0
1
0
0
0
Trichothelium minutum
1
1
1
1
0
1
1
0
0
0
0
1
0
0
Trichothelium pauciseptatum
1
1
1
1
1
1
1
1
1
1
1
1
1
1
Busambuli
Bukhaywa
Sporopodium leprieurii
Buyangu
Species
242
Appendix 15. Frequency of occurrence of species in the samples of the forest parts of Kakamega. D = dominant, VF = very
Salazar
Yala
Malava
Kisere
Kaimosi
Isiukhu
Isecheno
Ikuywa
Ghostisland
Colobus
Campsite
Buyangu
Busambuli
Species
Aderkomyces dilatatus
Arthonia atropunctata
Arthonia flavoverrucosa
Arthonia fuscocyanea
Arthonia lividula
Arthonia orbygniae
Aspidothelium fugiens
Aspidothelium geminiparum
Aspidothelium scutelicarpum
Aspidothelium hirsutum sp. nov.
Asterothyrium aulaxinoides
Asterothyrium leucophthalmum
Asterothyrium microsporum
Asterothyrium pittieri
Asterothyrium rotuliforme
Asterothyrium septemseptatum
Asterothyrium sp.
Aulaxina epiphylla
Aulaxina opegraphina
Bacidia medialis
Bacidina apiahica
Bacidina mirabilis
Bacidina pallidocarnea
Bacidina simplex
Badimia dimidiata
Bapalmuia ivoriensis
Bukhaywa
frequent, F = frequent, LS = less frequent, O = Occasional, R = rare
R
R
R
R
R
R
R
R
R
R
R
R
O
R
R
R
O
R
R
R
R
R
R
VF
R
R
R
R
O
R
VF
R
R
R
R
R
O
D
R
R
R
R
F
O
R
O
R
O
R
VF
O
R
R
O
R
R
R
R
F
R
R
R
F
O
R
O
O
D
R
O
R
R
R
R
R
243
R
D
D
R
F
O
D
R
O
R
R
R
R
R
R
O
F
O
F
O
VF
F
O
R
R
F
F
F
F
VF
O
R
F
O
R
F
O
F
R
R
VF
F
R
O
R
O
R
R
O
F
F
R
O
O
R
R
F
R
R
R
O
VF
R
F
O
R
O
R
R
R
D
F
R
F
R
F
R
F
F
R
F
D
F
R
R
O
R
R
R
R
R
R
O
R
O
O
F
O
VF
O
D
R
O
O
O
R
R
R
F
R
O
O
R
R
R
R
O
O
R
F
R
O
F
R
R
O
O
R
R
R
R
R
F
O
O
F
F
R
F
O
R
R
R
O
O
R
R
F
R
F
O
F
F
R
Yala
R
D
R
R
Salazar
R
Malava
O
Kisere
Kaimosi
Isiukhu
Isecheno
Ikuywa
Ghostisland
Colobus
Campsite
Buyangu
Busambuli
Bukhaywa
Species
Biatora sp.
Brasilicia dimerelloides
Brasilicia foliicola
Byssolecania deplanata
Byssolecania hymenocarpa
Byssolecania variabilis
Byssoloma chlorinum
Byssoloma leucoblepharum
Byssoloma subdiscordans
Calenia aspidota
Calenia bullatinoides
Calenia depressa
Calenia graphidea
Calenia monospora
Calenia sp.
Calenia thelotremela
Calopadia fusca
Calopadia puiggarii
Calopadia subcoerulescens
Chroodiscus australiensis
Chroodiscus kakamegensis sp. nov.
Chroodiscus verrucosus
Coccocarpia stellata
Coenogonium dilucidum
Coenogonium fallaciosum
Coenogonium flavum
Coenogonium geralense
Coenogonium lisowskii
Coenogonium pocsii
Coenogonium siquirrense
O
O
O
R
R
O
VF
D
R
R
F
R
O
O
F
O
O
VF
244
O
R
R
R
O
O
VF
F
R
R
O
R
R
R
F
F
O
O
R
R
R
VF
O
O
O
R
O
O
VF
O
R
F
R
R
R
R
R
O
R
R
O
VF
O
R
R
R
O
R
O
VF
O
R
VF
Yala
Kaimosi
Isiukhu
Isecheno
R
F
R
Ikuywa
Ghostisland
O
Salazar
R
R
Malava
R
Colobus
Campsite
R
Kisere
O
Buyangu
Busambuli
Bukhaywa
Species
Coenogonium sp.
Coenogonium subdilucidum
Coenogonium subfallaciosum
Coenogonium subluteum
Coenogonium usambarense
Coenogonium zonatum
Echinoplaca diffluens
Echinoplaca pellicula
Enterographa fellhaneroides sp.nov.
Enterographa meklitiae sp.nov.
Eremothecella calamicola
Fellhanera bouteillei
Fellhanera aff. bouteillei
Fellhanera encephalarti
Fellhanera paradoxa
Fellhanera parvula
Fellhanera rhaphidophylli
Fellhanera subfuscatula
Fellhanera sublecanorina
Fellhanera submicrommata
Gyalectidium caucasicum
Gyalectidium eskuchei
Gyalectidium filicinum
Gyalectidium fuscum
Gyalectidium imperfectum
Gyalidea epiphylla
Gyalidea psorotheciopides sp. nov.
Gyalideopsis cochlearifer
Lasioloma arachnoideum
Lichenopeltella epiphylla
R
R
O
R
R
R
R
O
D
R
R
R
O
R
F
D
R
R
R
R
O
O
R
R
R
F
F
R
F
R
VF
VF
R
VF
R
O
D
F
VF
D
F
R
R
R
F
R
O
R
R
O
O
R
O
R
R
R
R
R
O
F
R
R
R
F
R
245
O
D
R
D
O
F
R
O
O
R
R
R
O
F
R
R
D
R
D
R
VF
O
D
D
VF
D
R
D
R
D
VF
D
VF
R
D
O
R
O
VF
Yala
O
O
Malava
R
O
Kisere
F
Kaimosi
VF
F
R
R
R
VF
F
R
O
VF
Salazar
O
Ikuywa
Ghostisland
Colobus
Campsite
R
O
Isiukhu
F
F
R
R
R
O
R
O
R
R
R
Isecheno
D
O
Buyangu
Busambuli
Bukhaywa
Species
Loflammia epiphylla
Lyromma nectandrae
Mazosia melanopthalma
Musaespora kalbii
Opegrapha epiporina
Opegrapha phylloporinae
Opegrapha sp.
Opegrapha velata
Phylloblastia pocsii
Phyllospora sp.
Porina atrocoerulea
Porina cf. triseptata
Porina cupreola var. cupreola
Porina distans
Porina epiphylla
Porina epiphylloides
Porina kamerunensis
Porina leptosperma
Porina limbulata
Porina lucida var. lucida
Porina mazosoides
Porina pallescens
Porina nitidula
Porina rubentior
Porina rubescens
Porina rufula
Porina semicarpi
Porina sphaerocephaloides
Porina subpallescens
Porina tetramera
F
F
D
R
F
F
R
R
D
R
D
O
D
R
D
D
R
D
D
O
D
VF
R
R
R
R
D
D
F
R
F
D
D
F
R
R
R
R
R
D
D
D
R
VF
VF
D
D
R
R
R
VF
R
O
R
R
O
R
D
F
R
D
D
D
D
D
O
D
D
O
O
F
R
O
D
D
R
R
F
D
F
O
F
D
D
R
D
D
R
R
D
D
R
F
R
246
O
O
VF
O
F
F
VF
D
D
R
R
R
R
D
R
R
F
F
R
R
O
O
D
R
D
F
O
R
O
VF
F
R
O
O
Yala
R
R
Salazar
Kaimosi
Malava
F
Kisere
R
Isiukhu
Isecheno
Ikuywa
Ghostisland
Colobus
Campsite
Buyangu
Busambuli
Bukhaywa
Species
Porina trichothelioides
Psorotheciopsis gyalideoides
Psorotheciopsis patellarioides
Psorotheciopsis varieseptata
Sporopodium antonianum
Sporopodium leprieurii
Sporopodium pilocarpoides
Sporopodium sp.
Strigula antillarum
Strigula concreta
Strigula janeriensis
Strigula macrocarpa
Strigula maculata
Strigula melanobapha
Strigula microspora
Strigula nemathora var. hypothelia
Strigula nemathora
Strigula nitidula
Strigula obducta
Strigula phyllogena
Strigula schizospora
Strigula smaragdula
Strigula subtilissima
Tapellaria epiphylla
Tapellaria nigrata
Tricharia vainioi
Trichothelium africanum
Trichothelium epiphyllum
Trichothelium minutum
Trichothelium pauciseptatum
R
F
R
F
R
O
R
R
R
O
F
R
R
R
O
F
R
R
F
R
R
D
O
O
F
O
R
R
O
R
D
R
D
R
F
VF
O
VF
F
O
D
R
D
F
VF
F
F
VF
O
R
R
O
F
O
D
F
VF
R
D
O
R
O
F
O
F
F
O
O
O
R
R
F
O
VF
O
F
R
R
O
F
R
D
O
F
R
O
D
O
D
O
VF
R
R
F
D
R
R
R
R
R
R
R
F
O
O
R
R
R
R
F
R
R
R
R
O
O
O
F
VF
O
R
R
O
O
R
VF
O
R
F
F
R
R
O
VF
247
Appendix 16. Distribution of foliicolous lichens in the forest sites of Godere, Budongo and Kakamega.
Ghostislanid
Ikuywa
Isecheno
Isikuhu
Kaimosi
Kisere
Malava
Salazar
Yala
Old secondary
Primary
Swamp
Young secondary
Asterothyrium sp.
Aulaxina epiphylla
Aulaxina microphana
Aulaxina opegraphina
Bacidia medialis
Bacidina apiahica
Bacidina mirabilis
Dushi
Asterothyrium septemseptatum
Colobus
Asterothyrium microsporum
Asterothyrium monosporum
Asterothyrium octomerum
Asterothyrium pittieri
Asterothyrium rotuliforme
Camp site
Asterothyrium leucophthalmum
Busambuli
Asterothyrium aulaxinoides
Buyangu
**Aspidothelium hirsutum sp. nov.
ADEDI
ARTAT
ARTFL
ARTFU
ARTLI
ARTOR
ASPFU
ASPGE
ASPHI
ASPSC
ASTAU
ASTLE
ASTMI
ASTMO
ASTOC
ASTPI
ASTRO
ASTSE
ASTSP
AULEP
AULMI
AULOP
BACAP
BACME
BACMI
Bukhaywa
Aderkomyces dilatatus
Arthonia atropunctata
Arthonia flavoverrucosa
Arthonia fuscocyanea
Arthonia lividula
Arthonia orbygniae
Aspidothelium fugiens
*Aspidothelium geminiparum
*Aspidothelium scutelicarpum
Bishan Waka
Species acronym
1 = presence, 0 = absence. * = new to Africa, ** new to science
0
0
0
0
0
0
1
0
0
0
0
1
0
0
0
0
1
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
1
1
0
0
1
0
0
0
0
0
0
0
0
0
1
0
0
1
0
0
0
1
1
0
0
0
0
1
0
0
0
0
0
1
1
1
0
0
1
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
1
1
0
0
0
1
1
1
1
1
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
1
0
0
1
0
1
0
0
1
0
0
1
0
1
0
1
0
0
0
0
0
0
1
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
1
0
0
0
0
0
1
0
1
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
1
1
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
1
1
1
1
1
0
0
0
1
0
0
0
0
0
0
1
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
1
0
0
1
0
0
0
0
0
0
0
1
0
0
1
0
0
0
1
0
0
0
0
0
0
1
1
0
0
0
0
1
0
0
0
0
0
0
0
1
0
0
0
1
0
0
0
0
0
1
1
0
0
0
0
0
0
0
1
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
1
1
0
0
0
0
1
1
1
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
1
1
0
0
0
0
1
0
1
0
0
0
0
0
1
1
0
0
0
0
0
0
0
0
0
1
1
0
0
0
0
0
1
0
1
0
0
0
0
1
1
0
0
0
0
0
0
0
0
0
1
1
0
0
0
0
1
0
1
0
0
0
0
0
1
0
0
1
1
1
0
0
1
0
0
1
0
248
Buyangu
Busambuli
Camp site
Colobus
Dushi
Ghostislanid
Ikuywa
Isecheno
Isikuhu
Kaimosi
Kisere
Malava
Salazar
Yala
Old secondary
Primary
Swamp
Young secondary
Chroodiscus verrucosus
Bukhaywa
**Chroodiscus kakamegensis sp. nov.
BACPA
BACSI
BADDI
BAPIV
BAPPA
BRADI
BRAFO
BYSCH
BYSDE
BYSFU
BYSHY
BYSLE
BYSSD
BYSSP
BYSVA
CALAS
CALBU
CALDE
CALGR
CALMO
CALTH
CALTR
CALFU
CALPH
CALPU
CALSC
CAPGO
CHEVE
CHRAU
CHRKA
Bishan Waka
Species acronym
Bacidina pallidocarnea
Bacidina simplex
Badimia dimidiata
Bapalmuia ivoriensis
Bapalmuia palmularis
Brasilicia dimerelloides
Brasilicia foliicola
Byssolecania deplanata
Byssolecania fumosonigricans
Byssolecania hymenocarpa
Byssolecania variabilis
Byssoloma chlorinum
Byssoloma leucoblepharum
Byssoloma subdiscordans
Byssoloma subpolychromum
Calenia aspidota
Calenia bullatinoides
Calenia depressa
Calenia graphidea
Calenia monospora
Calenia thelotremela
*Calenia triseptata
Calopadia fusca
Calopadia phyllogena
Calopadia puiggarii
Calopadia subcoerulescens
**Caprettia goderei sp. nov.
Chroodiscus australiensis
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
1
0
1
0
0
0
0
1
1
1
0
0
0
1
0
0
0
0
0
1
1
0
0
0
0
1
0
1
0
0
1
0
1
0
0
0
0
0
0
1
1
0
0
1
0
0
0
0
0
0
1
1
0
1
1
1
1
1
0
0
1
0
1
0
0
0
1
1
1
0
0
0
0
0
0
0
0
0
0
1
1
0
0
1
0
1
1
1
0
0
1
0
1
1
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
1
0
1
0
0
0
0
0
0
0
0
0
1
0
1
0
0
0
0
0
0
0
0
0
1
1
0
0
0
1
0
0
1
0
0
1
0
1
0
0
0
0
0
1
0
0
0
0
0
1
0
0
1
0
1
1
0
1
0
0
0
0
1
0
1
1
1
1
0
1
0
1
1
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
1
0
0
0
1
0
0
1
0
1
0
0
0
1
1
0
1
0
0
0
1
1
1
0
0
1
1
1
0
0
1
0
1
1
1
0
0
1
0
1
1
0
1
0
1
0
1
0
0
0
0
1
0
0
0
0
0
1
0
0
1
0
0
0
1
0
0
1
0
1
1
0
0
1
1
0
1
1
0
0
0
1
0
0
0
0
1
1
1
0
1
0
1
1
1
1
0
1
0
1
1
0
0
0
1
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
1
0
0
0
1
0
0
1
0
1
1
0
0
1
0
0
1
0
0
0
0
1
1
0
1
1
1
1
0
0
0
0
0
1
1
0
0
1
0
1
0
0
0
1
1
1
1
0
0
0
0
0
0
0
0
0
1
1
0
0
0
0
0
0
1
0
0
1
0
1
0
0
0
1
1
0
1
0
1
0
1
1
0
0
0
0
0
1
0
0
1
0
1
1
1
0
0
1
0
1
1
0
0
1
1
0
0
0
1
0
1
1
1
0
0
1
1
1
0
0
1
0
1
1
1
0
0
1
0
1
1
0
0
0
1
0
1
0
0
0
1
1
1
1
1
0
1
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
1
1
1
1
1
1
1
1
1
0
0
1
0
1
1
1
0
0
0
1
0
0
0
0
1
1
1
1
0
0
1
1
1
1
1
1
1
0
1
1
0
0
1
0
1
1
0
0
0
1
0
1
0
0
1
0
1
0
1
0
0
0
1
1
1
1
1
1
1
1
0
1
1
1
1
1
0
0
0
1
0
1
0
0
1
0
1
249
Busambuli
Camp site
Colobus
Dushi
Ghostislanid
Ikuywa
Isecheno
Isikuhu
Kaimosi
Kisere
Malava
Salazar
Yala
Old secondary
Primary
Swamp
Young secondary
Eremothecella calamicola
Eugeniella wettsteinii
Fellhanera africana
Fellhanera aurantiaca
Fellhanera bouteillei
Fellhanera encephalarti
Fellhanera paradoxa
Fellhanera parvula
Fellhanera rhaphidophylli
Fellhanera subfuscatula
Fellhanera sublecanorina
Buyangu
**Enterographa meklitiae sp.nov.
Bukhaywa
**Enterographa fellhaneroides sp.nov.
COCST
COEBA
COEDI
COEFA
COEFL
COEGE
COELI
COEPA
COEPO
COESI
COESD
COESF
COESL
COEUS
COEZO
ECHDI
ECHPE
ENTFE
ENTME
ERECA
EUGWE
FELAF
FELAU
FELBU
FELEN
FELPA
FELPR
FELRH
FELSF
FELSL
Bishan Waka
Species acronym
Coccocarpia stellata
*Coenogonium barbatum
Coenogonium dilucidum
Coenogonium fallaciosum
*Coenogonium flavum
Coenogonium geralense
Coenogonium lisowskii
*Coenogonium pannosum
Coenogonium pocsii
*Coenogonium siquirrense
Coenogonium subdilucidum
Coenogonium subfallaciosum
Coenogonium subluteum
Coenogonium usambarense
Coenogonium zonatum
Echinoplaca diffluens
Echinoplaca pellicula
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
1
0
1
0
0
0
1
0
0
0
0
1
1
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
1
1
0
1
0
0
1
0
0
1
1
1
1
0
0
0
0
0
0
0
0
1
0
0
0
0
1
0
1
0
0
0
1
1
1
0
0
0
0
0
1
0
0
0
0
0
1
0
0
0
0
1
0
0
1
0
1
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
1
1
1
0
1
1
1
0
1
0
1
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
1
0
1
0
0
0
0
0
0
0
0
0
1
1
0
0
0
0
0
0
0
0
1
1
0
1
0
0
1
1
0
0
0
0
0
1
0
0
0
0
0
1
0
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
1
1
0
1
1
0
0
1
1
0
0
1
0
1
0
0
0
0
1
1
1
0
0
0
0
0
0
0
0
1
1
1
0
1
1
0
1
0
0
0
0
0
1
1
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
1
1
0
1
0
1
1
1
0
0
0
0
0
0
1
0
0
0
1
0
0
0
0
1
0
1
0
0
0
0
0
0
0
0
1
0
0
1
1
1
0
0
0
0
0
0
0
0
1
0
0
0
0
0
1
0
0
1
0
1
1
1
0
1
1
0
1
1
1
1
0
0
1
1
0
0
0
0
1
0
0
0
1
1
0
1
0
0
0
0
1
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
1
1
0
1
1
0
1
1
1
1
1
1
1
1
1
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
1
0
0
1
1
0
1
1
1
1
1
1
1
1
1
0
0
0
0
0
0
1
0
1
0
1
1
0
0
0
1
0
0
1
0
0
1
1
0
0
1
1
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
1
0
1
0
1
1
0
1
0
1
1
0
0
1
0
0
0
0
0
0
1
0
0
0
0
0
0
0
1
1
1
0
1
1
0
1
1
1
1
1
1
1
0
1
0
0
0
0
1
0
0
0
0
0
1
1
0
1
0
1
0
0
1
1
0
1
1
1
1
1
1
1
1
1
0
0
0
1
0
0
1
0
1
0
0
1
0
250
Buyangu
Busambuli
Camp site
Colobus
Dushi
Ghostislanid
Ikuywa
Isecheno
Isikuhu
Kaimosi
Kisere
Malava
Salazar
Yala
Old secondary
Primary
Swamp
Young secondary
Gyalideopsis cochlearifer
Lasioloma arachnoideum
Lichenopeltella epiphylla
Loflammia epiphylla
Lyromma nectandrae
Mazosia dispersa
Mazosia melanopthalma
Mazosia paupercula
Mazosia phyllosema
Mazosia rotula
Musaespora kalbii
Opegrapha epiporina
Opegrapha mazosiae
Opegrapha phylloporinae
Opegrapha sp.
Opegrapha velata
Phylloblastia pocsii
Porina alba
Porina atrocoerulea
Porina cf. triseptata
Porina conica
Bukhaywa
Gyalidea psorothecioides sp. nov.
FELSM
GYACA
GYAES
GYAFI
GYAFU
GYAIM
GYAMI
GYAEP
GYAPS
GYACO
LASAR
LICEP
LOFEP
LYRNE
MAZDI
MAZME
MAZPA
MAZPH
MAZRO
MUSKA
OPEEP
OPEMA
OPEPH
OPESP
OPEVE
PHYPO
PORAL
PORAT
PORCF
PORCO
Bishan Waka
Species acronym
Fellhanera submicrommata
Gyalectidium caucasicum
Gyalectidium eskuchei
Gyalectidium filicinum
Gyalectidium fuscum
Gyalectidium imperfectum
Gyalectidium microcarpum
Gyalidea epiphylla
0
0
0
1
1
1
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
1
0
0
1
0
1
0
0
0
1
1
0
0
0
0
1
0
1
0
0
0
0
1
0
1
1
1
1
0
0
1
0
0
1
0
1
1
0
0
0
1
0
1
0
0
1
0
1
0
0
0
1
1
0
1
0
0
0
0
0
0
0
1
1
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
1
1
0
0
0
0
0
0
0
1
1
1
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
1
0
0
0
0
0
1
0
1
0
0
0
0
0
0
1
0
1
1
0
0
0
0
1
0
0
1
0
1
0
1
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
1
1
0
0
0
1
0
0
0
1
1
0
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
1
0
1
0
0
0
0
0
0
0
1
0
1
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
1
0
1
0
0
0
1
0
0
0
0
0
1
0
0
0
0
0
0
0
0
1
0
0
1
0
0
0
0
0
1
0
1
0
1
0
1
0
1
1
0
1
1
0
1
0
0
0
0
1
0
1
0
1
0
0
1
0
0
1
0
0
1
0
1
0
0
0
0
0
0
0
1
0
0
0
0
0
0
1
0
1
0
1
0
0
0
0
0
1
1
0
1
0
0
0
1
0
0
0
0
0
1
0
1
0
0
0
0
0
0
1
0
1
1
0
0
1
0
0
0
0
1
1
1
0
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
1
1
0
0
0
0
1
0
0
1
0
1
0
0
0
0
0
0
0
1
0
1
0
1
0
0
0
0
1
0
0
0
0
1
0
0
1
0
0
1
0
1
0
0
0
1
0
0
0
0
0
1
0
1
0
0
0
0
0
0
1
0
0
0
0
0
1
0
1
0
0
1
0
1
0
0
0
0
0
1
0
1
0
1
0
1
1
0
1
1
1
1
0
0
1
0
0
1
1
0
0
1
0
1
0
1
0
0
0
1
0
1
1
1
0
1
1
0
0
0
0
0
0
0
1
0
1
1
1
1
1
1
0
1
0
1
0
0
0
1
1
1
1
1
1
1
1
0
1
0
1
0
0
0
1
0
0
1
1
0
0
1
1
1
1
1
0
0
0
0
0
1
1
1
0
1
1
0
1
0
1
1
0
0
1
0
1
1
251
Bukhaywa
Buyangu
Busambuli
Camp site
Colobus
Dushi
Ghostislanid
Ikuywa
Isecheno
Isikuhu
Kaimosi
Kisere
Malava
Salazar
Yala
Old secondary
Primary
Swamp
Young secondary
PORCU
PORDI
PORED
POREP
PORKA
PORLE
PORLI
PORLU
PORMA
PORNI
PORPA
PORRA
PORRB
PORRF
PORRU
PORSE
PORSH
PORSP
PORSU
PORTE
PORTR
PSOGY
PSOPA
PSOVA
SPOAN
SPOLE
SPOPH
SPOPI
STRAN
STRCO
Bishan Waka
Species acronym
Porina cupreola var. cupreola
Porina distans
Porina epiphylla
Porina epiphylloides
Porina kamerunensis
Porina leptosperma
Porina limbulata
Porina lucida var. lucida
Porina mazosoides
Porina nitidula
Porina pallescens
Porina radiata
Porina rubentior
Porina rubescens
Porina rufula
Porina semicarpi
Porina sphaerocephala
Porina sphaerocephaloides
Porina subpallescens
Porina tetramera
Porina trichothelioides
Psorotheciopsis gyalideoides
Psorotheciopsis patellarioides
Psorotheciopsis varieseptata
Sporopodium antonianum
Sporopodium leprieurii
Sporopodium phyllocharis
Sporopodium pilocarpoides
Strigula antillarum
Strigula concreta
1
0
1
0
0
1
0
0
0
1
0
0
1
0
0
0
0
0
1
0
0
0
1
0
0
0
1
0
0
0
1
1
1
0
0
0
0
0
0
1
0
0
1
0
0
0
0
0
1
1
0
0
1
0
0
0
0
0
1
0
1
0
1
1
0
1
1
1
1
1
0
0
1
0
1
1
0
1
1
0
0
0
0
1
1
1
0
1
1
0
1
0
1
1
0
0
0
0
0
1
0
0
1
0
0
0
0
0
1
0
0
0
0
1
0
0
0
0
1
1
0
0
1
0
0
0
0
0
0
1
0
0
1
0
0
0
0
0
0
0
0
1
1
1
0
0
0
0
0
0
1
0
1
0
1
0
1
0
0
1
0
0
1
1
0
0
0
0
1
0
1
0
1
0
0
0
0
0
0
0
1
0
1
0
0
1
0
0
0
1
0
0
1
1
1
0
0
0
1
1
1
0
0
1
1
1
1
0
0
0
1
0
1
0
0
0
0
0
0
1
0
0
1
1
0
1
0
0
1
0
0
0
1
0
0
0
0
0
0
0
1
0
1
0
0
0
0
0
0
1
0
0
1
1
0
1
0
0
1
0
0
0
1
0
1
0
0
1
0
0
1
1
1
1
0
0
0
0
0
1
0
0
1
1
1
1
0
0
1
0
0
0
0
0
0
0
0
0
1
0
1
0
1
1
0
0
1
0
1
1
0
0
1
0
0
1
0
1
1
0
1
0
0
0
0
1
0
1
1
0
1
1
1
0
0
0
0
0
0
1
0
0
1
1
1
0
0
0
1
0
0
0
0
0
1
0
0
0
0
0
1
0
1
1
0
0
1
0
0
1
0
0
1
1
0
0
0
0
1
0
0
0
1
1
0
0
0
0
0
0
1
0
1
0
0
0
0
0
0
1
0
0
1
1
1
0
0
0
1
0
0
0
1
1
0
0
0
0
0
0
1
0
1
1
0
1
0
0
1
1
1
0
1
1
1
1
0
0
1
1
0
0
0
0
1
0
0
1
0
0
1
0
1
1
0
1
0
0
0
1
0
0
1
1
0
1
0
0
1
1
0
0
0
0
1
1
0
1
0
1
1
0
1
0
1
1
0
0
0
1
0
1
1
1
1
1
1
0
1
0
0
0
0
0
0
0
0
0
0
0
1
0
1
1
1
1
0
0
0
1
0
1
1
1
1
1
1
1
1
0
0
0
0
0
1
1
0
1
0
0
0
0
1
1
0
1
0
0
1
1
0
1
1
1
1
1
1
1
1
0
0
0
1
0
1
1
1
1
1
0
1
0
1
1
1
1
1
0
0
1
0
1
1
1
0
1
1
1
1
1
1
0
1
0
1
1
0
0
1
0
252
Camp site
Colobus
Dushi
Ghostislanid
Ikuywa
Isecheno
Isikuhu
Kaimosi
Kisere
Malava
Salazar
Yala
Old secondary
Primary
Swamp
Young secondary
Tricharia vainioi
*Trichothelium africanum
Trichothelium alboatrum
Trichothelium epiphyllum
*Trichothelium minutum
Trichothelium pauciseptatum
Busambuli
**Tricharia nigriuncinata sp.nov.
Buyangu
Strigula nitidula
Strigula obducta
Strigula phyllogena
Strigula schizospora
Strigula smaragdula
Strigula subtilissima
Tapellaria bilimbioides
Tapellaria epiphylla
Tapellaria molleri
Tapellaria nigrata
Bukhaywa
Strigula nemathora var. hypothelia
Strigula nemathora var. nemathora
STRHY
STRJA
STRMA
STRMC
STRME
STRMI
STRMU
STRNE
STRNI
STROB
STRPH
STRSC
STRSM
STRST
TAPBI
TAPEP
TAPMO
TAPNI
TRINI
TRIVA
TRIAF
TRIAL
TRIEP
TRISP
TRIPA
Bishan Waka
Species acronym
Strigula janeriensis
Strigula macrocarpa
Strigula maculata
Strigula melanobapha
*Strigula microspora
Strigula multipunctata
0
0
0
0
0
0
1
1
1
0
1
0
1
0
0
0
0
0
0
0
1
0
1
1
1
0
1
0
0
1
0
1
1
1
1
1
0
1
0
0
0
0
0
0
0
0
0
1
1
1
0
1
1
1
1
0
1
0
1
1
1
1
1
0
0
0
0
0
0
1
1
0
1
1
1
0
1
0
0
1
0
1
0
1
1
1
1
1
0
0
1
0
0
0
1
1
0
0
1
1
0
0
0
0
1
0
0
0
1
0
0
0
1
0
0
0
0
0
0
0
0
0
0
1
1
0
1
0
0
1
0
1
0
1
1
1
1
1
0
0
0
0
0
0
0
1
0
1
0
1
0
1
0
0
1
0
1
0
1
0
1
1
1
0
1
0
0
0
0
0
1
0
1
1
1
0
1
0
0
1
0
0
0
0
0
1
1
1
0
0
0
0
0
0
0
1
0
0
1
1
1
1
0
0
1
0
1
0
1
1
1
1
1
0
0
0
0
0
0
1
1
0
0
1
1
0
1
0
0
1
0
1
0
1
1
1
1
1
1
0
0
0
0
0
0
0
0
0
0
1
0
1
1
1
1
0
0
1
1
1
1
1
1
0
0
1
0
0
0
1
1
0
1
0
1
0
0
0
0
0
0
1
0
1
0
1
1
1
1
0
0
0
0
0
1
1
0
0
0
1
0
1
0
0
1
0
1
1
1
1
1
1
1
0
0
0
0
1
0
0
0
0
0
0
1
0
1
0
0
1
0
1
0
1
1
1
1
1
0
0
0
0
0
0
0
0
0
0
1
1
0
1
0
0
1
0
1
0
1
1
1
1
1
1
0
0
0
0
0
1
0
0
0
0
1
0
1
0
0
1
0
1
0
1
1
1
1
1
1
0
0
0
0
0
1
0
0
0
0
1
1
1
0
0
1
1
1
1
1
1
1
1
1
1
0
0
0
0
0
0
1
0
1
0
1
1
1
0
0
1
1
1
0
1
1
1
0
1
1
0
0
0
1
1
1
1
1
1
0
1
1
1
1
0
1
1
1
1
1
1
1
1
1
1
0
0
0
0
1
1
1
1
1
0
1
1
1
0
0
1
1
1
1
1
0
1
1
1
1
0
0
1
0
0
1
1
0
1
1
1
253
Ghostislanid
Isikuhu
Buyangu
Colobus
Isecheno
Kisere
Ikuywa
Salazar
Yala
Young secondary
Old secondary
Primary
Swamp
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
Arthonia atropunctata
0
0
0
0
0
1
0
0
0
0
0
0
1
0
0
0
0
0
0
0
Arthonia flavoverrucosa
ARTFL
0
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
Arthonia fuscocyanea
ARTFU
0
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
Arthonia lividula
ARTLI
0
0
0
0
0
1
0
1
4
0
0
1
0
1
0
1
1
1
1
0
Arthonia orbygniae
ARTOR
0
0
0
0
0
0
0
0
2
0
0
0
0
0
0
1
0
0
0
1
Aspidothelium fugiens
ASPFU
0
1
0
0
0
3
0
0
1
1
0
0
0
2
1
1
1
0
1
0
Aspidothelium geminiparum
ASPGE
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
1
Aspidothelium hirsutum sp. nov.
ASPHI
0
0
0
0
0
1
0
0
0
0
0
0
1
0
0
0
0
0
0
0
Aspidothelium scutelicarpum
ASPSC
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
Asterothyrium aulaxinoides
ASTAU
1
0
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
Asterothyrium leucophthalmum
ASTLE
5
2
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
Asterothyrium microsporum
ASTMI
0
0
0
1
0
1
0
4
1
0
0
0
1
0
1
0
1
1
1
1
Asterothyrium monosporum
ASTMO
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
1
Asterothyrium octomerum
ASTOC
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
Asterothyrium pittieri
ASTPI
2
0
0
1
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
Asterothyrium rotuliforme
ASTRO
6
2
0
0
3
1
2
2
0
1
0
0
1
0
0
0
1
0
0
0
Asterothyrium septemseptatum
ASTSE
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
Malava
Buzambuli
0
ARTAT
Kaimosi
Bukhayawa
ADEDI
Dushi
Bishan Waka
Aderkomyces dilatatus
Species
Species acronym
Camp site
Appendix 17 Number of samples where species of foliicolous lichens were recorded in each forest site of Godere, Budongo and Kakamega forests
254
Buzambuli
Ghostislanid
Isikuhu
Buyangu
Colobus
Isecheno
Kisere
Ikuywa
Salazar
Yala
Young secondary
Old secondary
Primary
Swamp
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
Aulaxina epiphylla
AULEP
1
0
0
0
0
0
0
0
2
1
0
0
0
1
0
1
0
0
0
0
Aulaxina microphana
AULMI
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
Aulaxina opegraphina
AULOP
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
Bacidia medialis
BACME
0
0
0
0
0
0
0
2
0
0
0
0
0
0
0
0
0
0
0
0
Bacidina apiahica
BACAP
1
4
2
2
2
5
3
6
0
1
2
0
3
1
1
0
2
3
1
1
Bacidina mirabilis
BACMI
0
0
0
0
0
1
0
0
0
1
0
0
2
2
1
0
0
1
2
1
Bacidina pallidocarnea
BACPA
0
1
1
1
0
1
0
1
0
0
0
0
0
0
0
0
0
0
0
1
Bacidina simplex
BACSI
0
0
5
0
0
0
0
2
1
1
1
1
2
1
1
0
1
1
1
0
Badimia dimidiata
BADDI
0
0
0
0
0
0
0
0
1
1
0
0
0
0
0
0
0
0
0
0
Bapalmuia ivoriensis
BAPIV
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
1
0
0
1
1
Bapalmuia palmularis
BAPPA
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
1
Brasilicia dimerelloides
BRADI
0
0
1
0
0
0
0
0
0
1
0
0
0
2
2
1
1
1
1
1
Brasilicia foliicola
BRAFO
0
0
0
0
0
2
2
0
1
0
0
1
1
3
2
3
2
2
3
2
Byssolecania deplanata
BYSDE
0
0
0
0
0
0
0
0
0
0
0
0
1
2
0
4
2
1
3
2
Byssolecania fumosonigricans
BYSFU
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
1
2
1
Byssolecania hymenocarpa
BYSHY
0
0
0
0
0
2
0
0
0
0
0
0
1
0
0
0
2
3
2
1
Byssolecania variabilis
BYSVA
0
0
0
0
0
0
0
0
0
0
0
0
1
3
0
2
1
0
1
0
Byssoloma chlorinum
BYSCH
0
0
1
1
0
1
0
1
2
0
1
0
1
2
0
2
2
2
1
1
Malava
Bukhayawa
0
Kaimosi
Bishan Waka
1
Dushi
Camp site
ASTSP
Species acronym
Asterothyrium sp.
Species
255
Buzambuli
Ghostislanid
Isikuhu
Buyangu
Colobus
Isecheno
Kisere
Ikuywa
Salazar
Yala
Young secondary
Old secondary
Primary
Swamp
6
6
4
1
0
3
5
2
3
3
5
5
2
3
1
0
0
1
Byssoloma subdiscordans
BYSSD
0
0
0
0
0
0
0
0
1
1
0
0
0
0
0
0
0
1
0
0
Byssoloma subpolychromum
BYSSP
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
1
0
1
0
Calenia aspidota
CALAS
2
0
0
6
2
0
3
0
3
1
0
1
0
1
1
2
1
0
0
1
Calenia bullatinoides
CALBU
0
0
0
0
0
0
0
0
0
1
1
0
0
0
0
0
1
0
1
0
Calenia depressa
CALDE
2
0
1
4
0
0
0
0
3
1
0
0
0
3
1
1
2
0
1
1
Calenia graphidea
CALGR
0
0
0
4
0
0
0
0
4
1
0
0
1
3
1
1
2
0
1
1
Calenia monospora
CALMO
3
3
3
4
3
2
3
4
2
1
3
2
2
5
2
3
0
0
0
0
Calenia thelotremela
CALTH
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
Calenia triseptata
CALTR
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
Calopadia fusca
CALFU
0
3
2
1
3
4
2
1
1
1
2
3
1
1
2
1
1
0
2
1
Calopadia phyllogena
CALPH
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
Calopadia puiggarii
CALPU
0
6
6
4
2
3
4
3
3
1
1
3
2
5
3
2
1
0
0
1
Calopadia subcoerulescens
CALSC
0
0
0
1
0
0
2
0
1
0
0
1
0
3
1
1
0
0
0
0
Caprettia goderei sp. nov.
CAPGO
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
Chroodiscus australiensis
CHRAU
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
1
0
1
1
Chroodiscus kakamegensis sp. nov.
CHRKA
0
0
0
0
2
1
2
2
0
1
0
2
1
0
1
0
0
0
1
0
Chroodiscus verrucosus
CHEVE
1
1
0
4
4
1
0
1
3
1
0
2
2
2
1
2
1
0
1
1
Coccocarpia stellata
COCST
0
2
0
1
0
1
3
1
0
0
0
0
0
0
0
0
1
0
0
0
Malava
Bukhayawa
0
Kaimosi
Bishan Waka
0
Dushi
Camp site
BYSLE
Species acronym
Byssoloma leucoblepharum
Species
256
Buzambuli
Ghostislanid
Isikuhu
Buyangu
Colobus
Isecheno
Kisere
Ikuywa
Salazar
Yala
Young secondary
Old secondary
Primary
Swamp
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
Coenogonium dilucidum
COEDI
0
0
0
0
0
1
0
0
1
1
0
0
2
1
1
1
4
2
6
6
Coenogonium fallaciosum
COEFA
0
0
0
0
0
0
0
0
0
1
0
0
0
0
1
0
0
0
1
1
Coenogonium flavum
COEFL
0
0
3
4
0
0
0
0
0
0
1
2
1
0
0
0
0
0
0
0
Coenogonium geralense
COEGE
0
0
6
3
2
0
0
2
1
1
4
6
5
3
4
2
1
1
1
1
Coenogonium lisowskii
COELI
0
0
3
1
0
0
0
6
1
0
2
1
2
2
2
2
1
0
0
1
Coenogonium pannosum
COEPA
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
Coenogonium pocsii
COEPO
0
0
0
0
0
0
0
0
1
1
1
2
2
4
3
4
1
1
2
1
Coenogonium siquirrense
COESI
0
0
0
0
0
0
3
0
0
0
2
2
2
5
2
4
1
1
0
1
Coenogonium subdilucidum
COESD
0
0
0
0
0
0
0
0
1
0
1
0
0
0
1
1
1
0
1
1
Coenogonium subfallaciosum
COESF
0
0
0
0
2
0
0
0
1
2
0
2
1
0
3
2
1
0
0
1
Coenogonium subluteum
COESL
0
0
0
1
0
1
4
0
2
1
3
0
5
5
3
4
1
1
2
1
Coenogonium usambarense
COEUS
0
0
0
0
0
1
2
0
0
1
0
0
2
3
2
2
1
1
1
1
Coenogonium zonatum
COEZO
0
0
0
0
2
0
2
0
0
1
1
0
1
0
2
1
1
1
0
1
Echinoplaca diffluens
ECHDI
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
1
1
0
0
0
Echinoplaca pellicula
ECHPE
0
1
0
0
0
0
0
0
0
0
0
0
0
5
1
3
3
0
2
1
Enterographa fellhaneroides sp. nov.
ENTFE
0
0
0
0
0
0
0
0
0
0
0
1
1
0
0
0
0
0
0
0
Enterographa meklitae sp. nov.
ENTME
0
0
0
2
0
0
0
0
0
0
1
2
2
1
0
0
0
0
0
0
Eremothecella calamicola
ERECA
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
Malava
Bukhayawa
0
Kaimosi
Bishan Waka
0
Dushi
Camp site
COEBA
Species acronym
Coenogonium barbatum
Species
257
Buzambuli
Ghostislanid
Isikuhu
Buyangu
Colobus
Isecheno
Kisere
Ikuywa
Salazar
Yala
Young secondary
Old secondary
Primary
Swamp
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
Fellhanera africana
FELAF
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
Fellhanera aurantiaca
FELAU
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
Fellhanera bouteillei
FELBU
1
3
1
3
0
2
4
2
2
1
0
0
1
5
0
1
1
0
1
0
Fellhanera encephalarti
FELEN
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
Fellhanera paradoxa
FELPA
0
5
0
0
0
3
0
0
0
0
0
0
0
5
0
1
1
0
0
0
Fellhanera parvula
FELPR
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
Fellhanera rhaphidophylli
FELRH
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
1
0
0
0
1
Fellhanera subfuscatula
FELSF
0
0
0
1
0
2
0
0
1
1
0
0
1
0
1
2
1
0
0
1
Fellhanera sublecanorina
FELSL
0
1
0
2
0
1
2
0
0
0
0
0
0
0
0
0
0
0
0
0
Fellhanera submicrommata
FELSM
0
0
0
1
0
2
2
0
0
0
0
0
1
0
0
0
2
1
1
1
Gyalectidium caucasicum
GYACA
0
0
2
3
0
0
0
0
1
2
0
5
5
5
1
2
0
0
0
1
Gyalectidium eskuchei
GYAES
3
0
0
0
2
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
Gyalectidium filicinum
GYAFI
3
6
6
6
4
2
4
3
5
1
2
3
3
6
6
3
2
1
1
2
Gyalectidium fuscum
GYAFU
1
2
0
0
0
0
0
1
0
1
0
0
0
0
0
0
1
0
0
0
Gyalectidium imperfectum
GYAIM
3
1
0
0
0
2
3
2
1
0
0
0
0
2
0
0
2
1
1
1
Gyalectidium microcarpum
GYAMI
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
2
0
0
0
Gyalidea epiphylla
GYAEP
0
2
1
0
0
4
0
0
1
0
1
1
1
0
0
1
1
0
1
1
Gyalidea psorothecioides sp. nov.
GYAPS
0
0
1
0
0
0
0
1
0
1
0
0
0
0
0
0
0
0
0
0
Malava
Bukhayawa
0
Kaimosi
Bishan Waka
0
Dushi
Camp site
EUGWE
Species acronym
Eugeniella wettsteinii
Species
258
Buzambuli
Ghostislanid
Isikuhu
Buyangu
Colobus
Isecheno
Kisere
Ikuywa
Salazar
Yala
Young secondary
Old secondary
Primary
Swamp
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
Lasioloma arachnoideum
LASAR
0
0
0
0
0
0
0
0
3
1
0
0
0
0
0
0
0
0
0
0
Lichenopeltella epiphylla
LICEP
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
1
1
1
Loflammia epiphylla
LOFEP
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
1
Lyromma nectandrae
LYRNE
0
0
6
0
2
4
3
0
2
1
1
5
3
5
5
6
2
2
2
2
Mazosia dispersa
MAZDI
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
1
1
Mazosia melanopthalma
MAZME
0
0
2
0
0
0
0
0
5
2
2
0
2
3
1
2
2
6
6
3
Mazosia paupercula
MAZPA
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
Mazosia phyllosema
MAZPH
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
1
1
1
Mazosia rotula
MAZRO
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
4
1
5
4
Musaespora kalbii
MUSKA
0
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
Opegrapha epiporina
OPEEP
0
0
3
0
0
0
2
0
1
1
0
0
0
0
1
0
1
2
0
1
Opegrapha mazosiae
OPEMA
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
Opegrapha phylloporinae
OPEPH
0
0
3
1
0
0
2
1
2
2
1
4
1
1
0
2
1
2
0
1
Opegrapha velata
OPESP
0
0
1
1
0
1
2
0
2
0
2
0
1
0
0
0
0
0
0
0
Phylloblastia pocsii
OPEVE
0
1
1
0
0
0
0
0
0
0
1
2
1
0
1
0
0
0
0
0
Porina alba
PORAL
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
1
3
4
Porina atrocoerulea
PORAT
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
Porina aff. triseptata
PORCF
0
1
3
0
0
1
0
1
0
0
0
0
1
0
2
1
1
0
1
0
Malava
Bukhayawa
0
Kaimosi
Bishan Waka
0
Dushi
Camp site
GYACO
Species acronym
Gyalideopsis cochlearifer
Species
259
Buzambuli
Ghostislanid
Isikuhu
Buyangu
Colobus
Isecheno
Kisere
Ikuywa
Salazar
Yala
Young secondary
Old secondary
Primary
Swamp
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
1
1
3
Porina cupreola var. cupreola
PORCU
0
1
6
4
4
6
3
6
6
6
5
6
6
6
6
6
2
5
2
0
Porina distans
PORDI
0
0
1
0
0
0
3
0
0
0
0
1
0
0
0
0
0
0
0
0
Porina epiphylla
POREP
2
6
6
6
5
6
6
6
5
6
6
6
5
4
6
6
4
6
6
6
Porina epiphylloides
PORED
0
0
0
1
0
0
0
0
6
1
0
1
1
0
2
4
2
0
2
2
Porina kamerunensis
PORKA
0
0
0
0
0
0
0
0
0
0
1
0
0
0
0
0
2
6
2
0
Porina leptosperma
PORLE
0
2
0
0
0
5
0
0
0
1
0
0
0
0
1
1
2
1
1
2
Porina limbulata
PORLI
0
0
0
0
0
0
0
0
2
1
1
0
1
0
0
0
1
0
0
0
Porina lucida var. lucida
PORLU
0
0
0
0
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
Porina mazosoides
PORMA
0
0
0
0
0
0
0
0
1
1
0
0
0
0
1
0
0
0
0
1
Porina nitidula
PORNI
2
6
6
5
6
6
6
6
6
6
6
6
6
6
6
6
6
6
5
4
Porina pallescens
PORPA
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
0
0
Porina radiata
PORRA
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
3
4
6
4
Porina rubentior
PORRU
1
2
6
5
4
6
4
6
6
6
6
6
6
4
6
6
5
6
2
4
Porina rubescens
PORRB
0
0
0
0
4
1
3
1
0
0
1
2
1
4
3
2
2
4
1
2
Porina rufula
PORRF
0
0
0
0
0
1
2
1
0
1
0
2
0
0
1
0
0
3
1
2
Porina semicarpi
PORSE
0
0
0
0
2
0
0
0
1
1
0
1
0
3
3
3
1
2
4
3
Porina sphaerocephala
PORSP
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
3
4
3
3
Porina sphaerocephaloides
PORSH
0
0
0
0
0
0
0
0
1
1
0
0
0
0
0
0
2
0
1
1
Malava
Bukhayawa
0
Kaimosi
Bishan Waka
0
Dushi
Camp site
PORCO
Species acronym
Porina conica
Species
260
Buzambuli
Ghostislanid
Isikuhu
Buyangu
Colobus
Isecheno
Kisere
Ikuywa
Salazar
Yala
Young secondary
Old secondary
Primary
Swamp
6
4
2
6
3
6
3
5
6
6
4
6
6
4
2
1
1
1
Porina tetramera
PORTE
0
0
2
0
0
1
0
0
0
0
0
0
0
0
1
1
1
0
0
0
Porina trichothelioides
PORTR
0
0
0
0
0
1
0
0
1
0
1
0
0
0
0
0
1
0
0
0
Psorotheciopsis gyalideoides
PSOGY
2
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
Psorotheciopsis patellarioides
PSOPA
5
1
3
0
3
0
0
2
0
0
1
0
1
1
0
0
1
0
0
1
Psorotheciopsis varieseptata
PSOVA
3
0
0
2
0
1
0
2
0
1
0
0
1
0
0
0
0
0
0
0
Sporopodium antonianum
SPOAN
0
0
0
0
0
1
3
0
0
1
0
0
0
4
3
2
1
0
1
1
Sporopodium leprieurii
SPOLE
0
0
0
0
0
1
0
0
1
1
0
0
0
0
0
3
1
0
2
3
Sporopodium phyllocharis
SPOPH
0
1
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
1
Sporopodium pilocarpoides
SPOPI
0
0
0
0
0
0
0
0
1
1
0
0
0
1
1
1
0
0
1
1
Strigula antillarum
STRAN
0
0
2
6
0
0
0
0
2
1
0
2
0
0
0
0
1
0
0
1
Strigula concreta
STRCO
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
0
Strigula janeriensis
STRJA
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
1
1
1
1
Strigula macrocarpa
STRMA
0
0
5
3
3
1
0
2
4
3
2
3
2
3
4
1
1
1
1
1
Strigula maculata
STRMC
0
0
0
0
0
0
0
0
1
1
0
0
0
0
0
0
0
0
0
1
Strigula melanobapha
STRME
0
0
0
0
0
0
0
0
1
1
0
0
0
0
0
0
0
0
0
0
Strigula microspora
STRMI
2
0
2
6
2
1
0
1
2
2
3
5
2
5
3
1
3
3
3
3
Strigula multipunctata
STRMU
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
2
3
1
1
Strigula nemathora var. hypothelia
STRHY
0
1
3
1
0
2
3
2
0
2
1
3
1
2
2
2
5
4
2
3
Malava
Bukhayawa
6
Kaimosi
Bishan Waka
0
Dushi
Camp site
PORSU
Species acronym
Porina subpallescens
Species
261
Buzambuli
Ghostislanid
Isikuhu
Buyangu
Colobus
Isecheno
Kisere
Ikuywa
Salazar
Yala
Young secondary
Old secondary
Primary
Swamp
3
0
0
0
0
0
2
0
0
0
1
0
0
0
1
1
0
2
Strigula nitidula
STRNI
1
1
5
6
0
2
2
3
6
3
2
3
3
5
6
6
5
5
3
3
Strigula obducta
STROB
0
0
6
3
0
0
0
1
3
1
1
5
2
3
2
4
0
1
1
3
Strigula phyllogena
STRPH
0
6
6
4
4
4
3
6
5
5
6
4
5
4
6
4
4
6
5
6
Strigula schizospora
STRSC
0
0
0
2
2
1
2
2
1
1
1
2
2
1
2
1
1
1
0
1
Strigula smaragdula
STRSM
6
3
44
1
6
4
3
3
6
6
4
4
3
6
5
4
6
4
3
3
Strigula subtilissima
STRST
0
0
0
0
0
0
3
0
0
0
0
22
0
0
1
1
1
1
1
1
Tapellaria bilimbioides
TAPBI
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
Tapellaria epiphylla
TAPEP
0
0
0
1
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
Tapellaria molleri
TAPMO
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
Tapellaria nigrata
TAPNI
0
0
0
0
0
0
0
0
0
0
0
0
1
0
0
0
0
0
1
0
Tricharia nigriuncinata sp.nov.
TRINI
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
1
Tricharia vainioi
TRIVA
0
0
0
1
0
0
2
0
2
1
0
0
0
3
2
1
1
0
1
2
Trichothelium africanum
TRIAF
0
2
0
3
4
3
2
0
1
1
1
0
0
3
0
0
1
1
1
1
Trichothelium alboatrum
TRIAL
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
1
Trichothelium epiphyllum
TRIEP
0
1
1
0
0
1
0
0
1
1
1
0
0
0
0
0
1
1
1
1
Trichothelium minutum
TRISP
1
1
2
2
2
2
0
2
0
1
0
0
0
3
0
0
1
0
0
0
Trichothelium pauciseptatum
TRIPA
1
1
4
2
2
2
5
5
1
4
2
4
1
5
3
3
1
1
1
2
Malava
Bukhayawa
1
Kaimosi
Bishan Waka
0
Dushi
Camp site
STRNE
Species acronym
Strigula nemathora var. nemathora
Species
262
Acknowledgments
First of all I want to thank the Almighty God for giving me all the strengths to stay
away from my family and accomplish my work.
I would like to thank my wife Lily Fekade for shouldering all the burdens of taking
care of our children in my absence. Lily, you have a special place in my heart.
Brook, my son, has accompanied my wife during the whole time I was away.
Thank you Brook and I love you very much. My daughter, Meklit, was born during
my last year of study. In order to welcome her, I named one of the new species of
lichen I discovered after her. I would also like to thank the family of my wife and
my own family for visiting and supporting my wife and children.
My great thank goes to my supervisor Prof. Dr. Eberhard Fischer for accepting me
as a Ph. D. candidate in the University of Koblenz-Landau and for introducing me
the science of Lichenology. The effort of Prof. Fischer to train African students in
all fields of Botany is to be appreciated. Apart from academic issues, he was kind
enough to help me in private affairs.
I am grateful to Dr. Dorothee Killmann for providing me all the necessary advice
and support whenever I needed. I would like to thank Prof. Dr. Ulrich Sinsch, Dr.
Thomas Wagner, Ms. Brigitte Nilow-Lange, Ms. Dagmar Savelsberg and Dr. Inge
Theisen for their continual support during my stay in the Biology department. Prof.
Sinsch provided me softwares for multivariate and statistical analyses for which I
am grateful to him.
I wish to express my gratitude to Prof. Emmanuël Sérusiaux from Liége University
in Belgium who had assisted me in dealing with the most difficult lichen
specimens. He also provided me good hospitality during my stay in Liége.
During my fieldwork in Godere, Budongo and Kakamega I received logistic support
from the Tepi Coffee Plantation Enterprise in Ethiopia, Kenya Wildlife Service,
National Museums of Kenya, and the Budongo Forest Project in Uganda. I want to
thank the staffs these organizations that provided me support. Itambo Malombe
263
had accompanied me during the first week of my stay in Kakamega. Bunny
Dumbo had helped me during the field work in Budongo. I thank them very much.
I received moral support for my study in Lichenology from Prof. Sebsebe
Demissew, Dr. Ensermu Kelbesa, Prof. Zerihun Woldu, Dr. Tamrat Bekele, Prof.
Masresha Fetene, Dr. Sileshi Nemomissa, Dr. Girma Balcha, Dr. Kassahun
Embaye, Dr. Tesfaye Awas, Mr. Taye Bekele, Dr. Teshome Sormessa and other
staffs of Addis Ababa University and the Institute of Biodiversity in Ethiopia. I thank
all of them.
I received a scholarship for the PhD study from the German Catholic Academic
Exchange Service (KAAD) and the German Ministry of Education and Research
(BMBF) partially financed my scholarship. I am very much grateful for both
organizations. Dr. Thomas Scheidtweiler, Dr. Marko Kuhn and Ms. Simone Saure
of KAAD deserve special thanks for facilitating my scholarship.
Last but not least, I want to thank all my friends and relatives who provided me
and my family moral supports.
264
DECLARATION
I declare that this dissertation is my independent original work, it or part of it has
not been presented in any other University and that all sources of materials used
for the dissertation have been duly acknowledged.
Name:
Kumelachew Yeshitela
Signature:
___________________________
Date of submission: _____________________________
265