Professional Documents
Culture Documents
S5f I T H S O S I A S I K S T I T U T I O K PRESS
City of IVashington
1976
ABSTRACT
iii
A Monograph of the Lichen Genus
Pseudoparmelia Lynge (Parmeliaceae)
1
2 SMITHSONIAK CONTRIBUTIONS T O BOTANY
These include Mr. Peter James (BM), Dr. A. J. even at the margin. T h e degree of adnation varies
Kostermans (BO), Dr. A. Robyns (BR), Mr. M. S. from nearly subcrustose in P. xanthomelaena (Fig-
Christiansen (C), Dr. M'. A. Weber (COLO), Dr. W. ure 18e) to loosely adnate in P. caperata. Compa-
L. Culberson (DUKE), Dr. L. Williams (F), Dr. I. rable eciliate species of Parmotrema have wider,
M. Lamb (FH), Dr. C. E. Bonner (G), Mr. C. E. more or less marginally erect lobes. Lobe configura-
Palmar (GLAM), Dr. T . Ahti (H), Dr. H. Schindler tion is variable. While some species have sublinear,
(KR), Dr. J. Poelt (M), Dr. H . A. Imshaug (MSC), apically obtuse lobes 0.5-2.0 mm wide (Figures 6b,d,
Dr. H. Osorio (MVM), Dr. C. T. Rogerson (NY), Dr. 10e, 12d), an even larger number have subirregular,
Hildur Krog (0),Dr. E. F. Warburg (OXF), Mme. apically rotund lobes 2-6 mm wide (Figures 6a,c,
Jovet-Ast (PC), Dr. C. E. Smith (PH), Dr. S. Ahlner 9a, IOc, 12c). Lobes in both types are often contigu-
(S), Dr. S. Kurokawa (TNS), Dr. R . Alava (TUR), ous and crowded. There is no marginal ornamenta-
Dr. I. Tavares (UC), Dr. R . Santesson (UPS), Dr. H. tion i n Pseudoparmelia; the margins are smooth and
Riedl (W), Dr. J. W. Thomson (WIS), and Dr. G. sometimes black rimmed.
Cufodontis (TNU). Dr. Ove Almborn (LD) lent his T h e lower surface of the thallus is either black
own extensive collections in addition to materials or pale brown, and this color difference, although
from BOL, L, PRE, and T R H which he had on variable in some of the saxicolous species, can be
hand for study. Dr. Z. Cernohorskj kindly arranged an important taxonomic character. Broader lobed
for loans from BP at a time when travel in Hungary species with a black lower surface, such as the well-
was not permitted. T h e late Dr. H. des Abbayes known P. caperata, usually have a narrow brown
(REN) was extremely generous in sending loans as zone at the lobe tips. While most species have a
well as duplicates of type-collections of the new shiny paraplectenchymatous lower surface (Figure
species he was describing. For allowing me to ex- Ic), species in the P. amplexa group (P. amplexa, P.
amine collections in their private herbaria, I am pachydactyla, and P. subamplexa) have a minutely
especially indebted to Dr. D. D. Awasthi, Dr. Gun- grained, velvety appearing black lower surface to
nar Degelius, Dr. M. Mahu, Dr. T . D. V. SB' 'inscow, the margin (Figure la,b). This is caused by an ir-
and Dr. Rolf Santesson. regularly thickened, minutely papillose cell layer
T h e specimens were photographed by the Smith- sloughing from the lower cortex, a phenomenon
sonian Office of Printing and Photographic Ser- which I have not seen in any other parmelioid
vices. Scanning-electron microscope photographs genera.
were prepared by the Smithsonian Scanning-Elec- Rhizines are uniformly simple and produced in
tron Microscope Laboratory. moderate abundance (Figure Id). T h e only excep-
Dr. S. Kurokawa assisted with species identifica- tion to this rule is P. intertexta, which usually has
tions, chemical tests, and descriptions prior to 1961, pale branched rhizines, not unlike those of some
and his help is gratefully acknowledged. Field species of Relicina but not as agglutinated (Hale,
studies have been supported at various times by the 19758). Broad-lobed species usually lack rhizines
National Science Foundation, National Geographic along the margins at lobe tips or at most have a
Society, Smithsonian Research Foundation, and the zone of short papillae. T h e rhizines are often blunt
Morden-Smithsonian Fund. Cooperative field with pale, penicillate tips (Reznik et al., 1968).
studies were conducted in India with the Maharash- T h e internal structure of Pseudoparmelia pre-
tra Association for the Cultivation of Science, work- sents no unusual features (Figure Za,c,f). T h e upper
ing with Dr. P. G. Patwardhan, and in Venezuela cortex has a basic palisade structure (Figure 2 d ) and
with Dr. M. Lopez-Figueiras of the Universidad de is overlain by a thin pored epicortex (Figure le,f),
10s Andes. Finally, I wish to thank Dr. Ove Alm- as I had previously discovered by using the
born for reading the entire manuscript and check- scanning-electron microscope (Hale, 1973a). T h e
ing the bibliography and spelling of place names. medullary hyphae are often conspicuously encrusted
with lichen substances. T h e lower cortex is para-
plectenchymatous (Figure 2e). I n these respects it
Morphology is identical with the other epicorticate genera in the
THALLw-The thallus is typically foliose, orbic- family.
ular, 3-15 cm in diameter, and uniformly adnate, VEGETATIVE PRoPAGuLES.-The isidia in Pseudo-
NUMBER 31 3
pavmelia are quite uniform. Twenty species (P. P. concomitaizs have the largest spores, u p to 24 pm
adspersa, P. amazonica, P. annexa, P. arcana, P. long.
basutoensis, P. caroliniana, P. cinerascens, P. con-
crescens, P. conlabiosa, P. cyphellata, P. dahlii (Fig-
Chemistry
ure Zg), P. ecapernta, P. ischnoides, P. malaccensis,
P. martinicana, P. neoquintaria, P. salacinifera, P. T h e chemical constitutents of Pseudoparmelia
scoiophylln, P. siibtovtzila, and P. venezolann) have were first summarized by Hale and Kurokawa (1964)
normal, cylindrical, simple to sparsely branched on the basis of microcrystal tests. I have retested
isidia. Two additional species ( P . p a c h y d a c t y l a and most of the species with thin-layer chromatography,
P. pn@illosa)have abnormally thickened but other- using solvent sjstems A and B of C. Culberson
wise normal isidia (Figure 14d). No species have (1972) and in large part confirming the earlier re-
lobulate, procumbent, or ciliate isidia. sults. T h e lichen substances in the genus are listed
Pustules have been described and illustrated for below under the presently accepted classification
Hypotrachynci (Hale, 1975a), and they are more or with number of species containing each substance
less the same in Pseudoparmelia (Figure 7 b ) , very i n parentheses.
thickened, fragile, hollow isidioid structures which
usually break open apically. Some then produce A\LIPHATIC ACIDS
soredia, while in other cases no soredia form. Seven Caperatic acid (5)
species (P. baltimorensis, P. eruptens, P. geesterani, Protolichesterinic acid (3)
P. owariensis, P. pustulescens, P. schistacea, and P. Others (2)
zim babzuensis) have largely nonsorediate pustules.
AROMATICC O \ l P O U N D S
One species (P. rnunkiaeri) has heavily sorediate
pustules. Orcinol Series
Ssralia occur in 14 species: P. alabamensis, P. para-Depsides
nptata, P. caperata, P. carneopruinata, P . crozalsi- DiLaricatic acid (9)
Erernic acid (1)
ana, P. cryptochlorophaea, P. epilezica, P. gerlachei, Gyrophoric acid (4)
P. labrosa, P. leucoxantha, P. soredians, P. subam- Lecanoric acid (4)
bigiin, P. subamplexa, and P. texana. They are usu- Obtusatic acid (1)
all) orbicular and discrete except in P. capevata, Perlatolic acid (2)
which has coalescent, more diffuse soralia. All are ineta-Depsides
Cr) tochlorophaeic acid (1)
strictly laminal except for P. leucoxantha (Figure Sekikaic acid (1)
13b), where the soralia are largely submarginal. I t is Depsidones
perhaps noteworthy that all of the sorediate species, Neoloxodic acid (2)
excepting P. alnbnmensis, are corticolous; sorediate, Soilobaridone (3)
obliqately saxicolous species are very rare in the p-Orcinol Series
genus. para-Depsides
T h e remaining 32 species lack any vegetative Atranorin ( 5 5 )
propagules. T h e older lobes, however, may become Barbatic acid (1)
4-0-Demethylbarbatic acid (1)
lobulate or heavily rugose, although, as pointed out
Depsidones
above, no species have true laminal lobulae (phyl- Constictic acid ( 5 )
lidia) or lobulate isidia. Virtually all of these species Fumarprotocetraric acid (1)
are fertile. Norstictic acid (2)
APoTHECIA.-Apothecia, found so far in 47 of Physodalic acid ( 2 )
Protocetraric acid (25)
the 76 species, are extremely uniform. They are
Salazinic acid ( 5 )
sessile to subpedicellate and 1-3 mm (rarely t o 6 Stictic acid (8)
nim) in diameter. T h e disc is always imperforate. Succinprotocetraric acid (1)
T h e asci contain eight spores, and the bulk of the
species have spores in the range of 6-10 pm wide DIUESZOFURAXES
and 7-13 Ipm long. Psezidoparmelia caperata and Usnis acid (20)
6 S\IITHSOSI.AS COSTRIBUTIOSS TO BOTASY
babwensis are pustulate and have no obvious appears to be sympatric. T h e acids are particularly
relatives. interesting since sekikaic acid is a meta-depside
There is a particularly interesting group of saxi- and divaricatic acid the homologous para-depside
colous species in South Africa, including P. molyb- (Figure 4).
diza (lecanoric acid), P. spodochroa (salazinic acid), Rarer species with chemical differences used as
P. tortula (norlobaridone), and P. vanderbylii (un- taxonomic characters include P. dahlii (lecanoric
known depsides). They are so similar externally acid) and P. rahengensis (barbatic acid group) in
that chemical tests are needed to separate them. Southeast Asia. Pseiidoparmelia rutidota, a common
IVhile this group may have evolved from a common species in Australia and southwestern United States
parent, the chemical evolution has followed very into tropical America, contains protocetraric acid;
different pathways. T h e presumptive isidiate a virtually indistinguishable population, P. exor-
morphs of three of these (P. antzexa, P. scotophylla, nata, contains protocetraric acid with the confor-
and P. subtortula) are also sufficiently similar that mata unknown and occurs principally in Uruguay.
chemical tests are required for positive identifica- Other close relatives include P. ferax, which con-
tion. tains physodalic acid, and P. callichroa, which con-
If one subscribes to the concept of vegetative tains a fatty acid.
morphs, it then follows that morphologically identi- T h e presence or absence of usnic acid is the main
cal but chemically different vegetative morphs have criterion for recognizing P. nairobiensis (usnic acid
evolved from different parents through parallel evo- absent in the cortex) and P. zambiensis (usnic acid
lution and are therefore polyphyletic (W. Culberson, present) and their corresponding isidiate morphs,
1973). Pseudoparmeliu texana (divaricatic acid) and P. concrescens and P. ecaperata.
P. uptutu (perlatolic acid), for example, differ in
distribution, P. texana being pan-temperate whereas
P . aptatu occurs only in the Old World. T h e two Phytogeography
acids involved are para-depsides, divaricatic acid
T h e Psezidoparmelia floras of various geopolitical
having a C,H, side chain and perlatolic acid C5Hll
units are listed below. Many countries are so poorly
side chains (Figure 4). Another chemical pair, P.
collected, of course, that no meaningful floristic
owariensis (divaricatic acid) and P. pustulescens
comparisons can be made. However, the United
(sekikaic acid), is confined to the Old World and
States, West Indies, Venezuela, South Africa, and
perhaps Brazil and Australia are all rather well
known. Several lichenologists are now working in
R East Africa and Australia, and their studies, when
A,,--CO-0 - 0 - O H completed, will fill in many gaps.
NORTHAMERICA
CH~O-V-OH -COOH
I Canada: P. baltimorensis, P . caperata.
R United States: P . alabamensis, P . amazonica, P. baltirnoren-
sis, P. caperata, P . caroliniana, P. crozalsiana, P. crypto-
chlorophaea, P . martinicana, P. rutidota, P. salacinifera, P.
sphaerospora, P. texana.
MEXICOA N D CENTRAL
AMERICA
Mexico: P. amazonica, P . carneopruinata, P. caroliniana, P .
crozalsiana, P . leucoxantha, P. martinicana, P. raunkiaeri,
P . rutidota, P . salacinifera, P. sphaerospora, P . texana.
Guatemala: P. caperata, P. sphaerospora.
Honduras: P. amazonica, P. carneopruinata, P. caroliniana,
P. cryptochlorophaea, P. salacinifera, P. texana.
Kicaragua: P. caroliniana.
FIGURE4.-Comparison of molecular structures of acids in Costa Rica: P . carneopruinata, P . caroliniana, P. sphaerospora,
Pseudopnrmelia: Divaricatic acid (R = C,H,) and perlatolic P. texana.
acid ( K = C,H,,) (above) and sekikaic acid (below). Panama: P. caroliniana, P. sphaerospora, P. texana.
NUMBER 31
Japan) has a rather small Pseudoparmelia flora of P. intertexta, (5), and P. owariensis (5). Within its
only 14 species, 4 of them endemic and the re- range P. caperata is undoubtedly the the most com-
mainder pantemperate or also widespread in Africa. monly collected foliose lichen, followed by P. caro-
I n general the Old World and New World floras liniana and i n Asia P. ecaperata.
are quite distinct. T h e Old World, however, is Twenty-nine species, nearly half the genus total,
much richer with about 55 species in contrast to have been found so far in only one country, as can
the 30 species so far collected i n North and South be determined from the lists of specimens examined
America. in the species treatment, and while many of these
Some idea of the abundance of the various spe- will be found in other countries with more intensive
cies can be gained by tabulating the number of collecting, this great a number reflects the high de-
countries (as listed above) where each species has gree of endemism characteristic of the genus.
been reported. This crude method of comparison
does not, of course, take into consideration the
relative sizes of the countries or the intensity of Taxonomic Treatment
collecting, but it is unlikely that the order of
abundance will be greatly changed by future col- T h e 7 6 species of Pseudoparmelia are arranged
lecting. T h e following species occiir in five or more below in alphabetic order. All specimens collected
countries: P. texana (24), P. caperata (17), P. sphae- by Hale are deposited in the Smithsonian Institu-
rospoi'a (16), P. caroliniana (13), P. amazonica (9), tion (US), and the herbarium acronym is not cited
P. canzeopminata (9), P. crozalsiana (Y), P. rutidota for these.
(9), P. salacinifera (B), P. ecaperata (7), P. aptata (7), T h e following key is divided into three sections:
P. concrescens (6), P. cryptochlorophaea (6), P. isidiate species, sorediate species, and nonisidiate,
malaccensis (6), P. martinicana (6), P. soredians (6), nonsorediate species.
KUMBER 31 11
ISIDIATE
I . Thallus greenish yellow (usnic acid present).
2. Thallus black below with at most a narrow brown zone at the lobe tips.
3. Isidia fine, n o more than 0.2 mm thick; medulla P - . . . . . . . . . P . ecaperata
3. Isidia thick and inHated, 0.5-1 nim thick; mzdulla P + retl.
4. Lower surface velvety black to the margin. . . . . . . . P . pachydactyla
4. 1,owrr surface shiny black with a narrow hrown ?one at the lobe tips.
5 . Isidia dense, cylindrical. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . papillosa
5 . Isidia irregularly scattered, often br.xking open apically. . . P . baltirnorensis
2. Thallus iiniformly pale brown hrlow.
6. Medulla P + retl (protocetraric acid). . . P . malaccensis
6 . Medulla P - .
7. Medulla C + red (Iccanoric acid). . . . . . . . . . . . . . . . . P . dahlii
i . Medulla C - or C + orange (barbatic acid). . . . . . . . . . . . . . P . rahengensis
1. Thallus whitish to greenish mineral gray (usnic acid lacking).
8. Collected on trees.
9. Lower surface uniformly pale brown.
10. Isitlia moderate to dense, 1 mm high: medulla K + red (salazinic acid). . . . . . . . . . .
.. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . salacirtifera
10. Isidia sparse, 2-3 mm high; medulla K - or K + yellow (stictic acid) . . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . cyphellata
9. Lower surface black toward the ccnter and black at the margin or with a narrow
brown rone at the lobe tips.
11. Isidia inHated, pustulate, 2-3 mm high . . . . . . . . . . . . . . . . . . . . . . . P . eruptens
11. Isidia not inflated or pustulate, to 1 mm high.
12. Upper surface finely reticulate!y cracked and strongly white-reticulate . . . . . .
..................................................... P . caroliniana
12. Upper surface continuous, not white-reticulate.
13. Medulla P - .
14. Medulla C + red (lecanoric acid). . . . . . . . . . . . . . . . P . conlabrosa
14. Medulla C - (divaricatic acid). . . . . . . . . . . . . . . P . concrescens
13. Medulla P + red or orange.
15. Medulla K + (salazinic acid) . . . . . . . . . . . . . . . . . . . . . . . . P . cinerascens
15. Medulla K - .
16. Fumarprotocetraric acid present. . . . . . . . . . . . . . . . . .P. . adspersa
16. Protocetraric acid present.
17. Isidia fragile, crumbling; lobe tips white-reticulate. . . . . . .
........................................ P . rnartinicana
17. lsidia normal; lobes not white-reticulate. . . . P . arnazonica
8. Collected on rocks.
18. Isidia coarse, pustulate, usually erupting apically.
19. Medulla K + red (salazinic acid). . . . . . . . . . . . . . . . . . . . . . . P . geesterani
19. Medulla K - .
+
20. Medulla P red (protocetraric acid). . . . . . . . . . . . . . P . simbabwensis
20. Medulla P - .
21. Divaricatic acid present. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . owariensis
21. Divaricatic acid absent.
22. Sekikaic acid present. . . . . . . . . . . . . . . . P . pustulescens
22. Caperatic acid present. . . . . . . . . . . . . . . . . . . . . . . . . . P . schistacea
18. Isidia normal, thin and cylindrical, not pustulate.
23. Medulla P + red or orange.
24. Lobes 2-3 mm wide, apically subrotund. . . . . . . . . . . . . . . . . P . scotophylla
24. Lobes about 1 mm wide.
25. Medulla K - ; collected in South America. . . . . . . . . . P . venesolana
25. Medulla K + ycllow (stictic acid); collected in Africa. . . . P . ischnoides
23. Medulla P - .
26. Lobes 2-4 mm wide, apically subrotund.
12 SMITHSONIAN CONTRIBUTIONS T O BOTANY
SOREDIATESPECIES
1. Thallus greenish yellow (usnic acid present).
2. Lower surface uniformly velvety black below to the margin. . . . . . . . . . . . P . subamplexa
2. Lower surface shiny, black at the center and dark brown in a narrow zone at the lobe tips.
3. Medulla K + yellow turning red (salazinic acid). . . . . . . . . . . . . . . . . . . . P . soredians
3. Medulla K-.
4. Medulla C + red (lecanoric acid), P-. . . . . . . . . . . . . . . . . . . . . . . P . subambigua
4. Medulla C-, P + red or orange.
5 . Soralia mostly laminal, becoming diffuse. . . . . . . . . . . . . . . . . . . . . . P . caperata
5 . Soralia mostly apical or marginal.
6. Soralia generally orbicular; collected in Antarctic regions or the high Andes.
. . . . . . ........................................... P . gerlachei
6. Soralia elongate along lobe margins; collected in mid-elevation tropical re-
gions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . leucoxantha
1. Thallus whitish to greenish mineral gray (usnic acid absent).
7. Medulla P + orange or red.
8. Upper surface broadly reticulately ridged and foveolate (without lens); stictic acid
present.
9. Lobes subirregular, 2-5 mm wide. . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . crozalsiana
9. Lobes sublinear, 1-2.5 mm wide. . . . . . . . . . . . . . . . . . . . . . . . . . . . P . carneopruinata
8. Upper surface smooth and plane; protocetraric acid present.
10. Soredia coarse, densely produced over the upper surface in coalescing soralia. , . . ,
...................................................... .. . P . raunkiaeri
10. Soredia farinose, produced in discrete orbicular soralia.
11. Collected on rocks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . aiabamensis
11. Collected on trees . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . epileuca
7. Medulla P-.
12. Medulla C + deep red (lecanoric acid). . . . . . . . . . . . . . . . . . . . . . . P . labrosa
12. Medulla C - or C + fleeting pink.
13. Soralia strongly capitate along lobe margins. . . . . . . . P . cryptochlorophaea
13. Soralia not capitate, entirely laminal.
14. Divaricatic acid present. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . texana
14. Perlatolic acid present. ................................. P . aptata
NONISIDIATE, SPECIES
NONSOREDIATE
1. Thallus greenish yellow (usnic acid present; P . chapadensis, P. hgpotnilta, and P . sphaerosporu
appear to be greenish yellow but lack usnic acid).
2. Lower surface brown or tan throughout.
3. Collected on trees. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . intertexta
3. Collected on rocks. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . chapadensis
2. Lower surface black.
4. Lower surface velvety black to the margin. . . . . . . . . . . . . . . . . . . . . . . . . . . P . amplexa
4 . Lower surface shiny black and often with a narrow brown zone at the lobe tips.
5 . Medulla P-.
6. Collected in Africa. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . zambiensis
6. Collected in South America. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . callichroa
N U M B E R 31 13
3. Medulla P + red.
7 . Physodalic acid present. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . ferax
7. Physodalic acid absent.
8. Protocetraric acid present. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . rutidota
8. Protocetraric acid and the conformata unknown present. . . . . . . P . exornata
1. Thallus whitish to greenish mineral gray (usnic acid absent; P . chapadensis, P . hypomilta,
P. sphaerospora, and sometimes P. violacea appear to be yellowish green but lack usnic acid).
9. Medulla pigmented purple to yellow.
10. Medulla completely deep purple. . . . . . . . . . . . . . . . . . . . . . . . . . . . P . uiolacea
10. Medulla yellow or orange.
11. Medulla completely pale orange-yellow ( P . condyloides appears yellow but con-
tains no pigment.) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . sphaerospora
11. Medulla pigmented only in the lower half.
12. Collected on rocks. . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . lecanoracea
12. Collected on trees.
13. Lower surface brown; collected in South America. . . . . P. hrpomilta
13. Lower surface hlack; collected in Australia. . . . . . . . . . . . P . corrugatiua
9. Medulla white.
14. Collected on trees.
15. Lower surface uniformly brown.
16. Medulla P + red (protocetraric acid). . P . somaliensis
16. Medulla P- or P + faint orange (stictic acid).. . . . . . . . . . . . . P . sphaerospora
15. Lower surface black (often with a narrow brown zone at the lobe tips).
17. Medulla P - .
18. Collected in Africa; divaricatic acid present. . . . . . . . . . P . . nairobiensis
18. Collected in Australia and New Zealand; caperatic acid present. . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . subtiliacea
17. Medulla P + red or orange.
19. Medulla K + yellow (stictic acid); surface of lobes reticulately ridged
and foveolate (without lens).
20. Lobes 1-2 mm wide; collected in South America. . . . P . scrobicularis
20. Lobes 2-4 mm wide; collected in Africa. . . . . . . . . . . P . inhaminensis
19. Medulla K - (protocetraric acid).
21. Lobes 1-2 mm wide. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . schelpei
21. Lobes 3-6 mm wide.
22. Medulla C-; collected in the West Indies . . . . . . P . inornata
22. Medulla C + rose; collected in New Caledonia. . . . . . . . . . . . . . .
....... . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . , . . P . concomitans
14. Collected on rocks.
23. Lower surface uniformly brown.
24. Medulla P + orange (salazinic acid).
25. Chalybeizans unknown present. . . . . . . . . . . . . . . . . . . . . P. condyloides
25. Chalybeizans unknown absent. . . . . . . . . . . . . . . . . . .P. . spodochroa
24. Medulla P-.
26. Medulla C + red (lecanoric acid). . . . . . . . . . . . . . . . . . . . P . molybdiza
26. Medulla C-.
27. Thallus rather loosely attached on rocks and soil; lobes subelongate.
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . P . prolata
27. Thallus tightly adnate on rocks; lobes shorter, apically rotund.
28. Norlobaridone present. . . . . . . . . . . . . . . . . . . . . . . . . . . . P . tortula
28. Unknown substances present. . . . . . . . . . . . . . . . . P. . uanderbylii
23. Lower surface black (brown only in a narrow zone at the lobe tips).
29. Medulla P + orange or red.
30. Lobes less than 1 mm wide. . . . . . . . . . . . . . . . . . . . . . P . xanthomelaena
30. Lobes 2-4 mm wide.
31. Medulla K-; collected in the Caribbean region . . . . . . P . caribaea
31. Medulla K + yellow or red (salazinic acid); collected in Australia
and Africa. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . p . spodochroa
29. Medulla P-.
32. Collected in South America. , . , . , . , . . , , , . , , , . . , , , , , . p . rupicola
, , , ,
14 SMITHSONIAN CONTRIBUTIONS T O BO TA N I
cies, P. epileuca (Hale) Hale, also has soredia and Pseudoparmelia amplexa
protocetraric acid, but it is corticolous and has
broader lobes. FIGURE6d
SpEcrhrms ExAar1sED.-United States: Tennessee, Hale Pseudoparmelia amplexa (Stirton) Hale, 1974: 189.
36927. Parmelia amplexa Stirton, 1877:212 [type collection: Somer-
set East, Union of South Africa, MacOu'an (BM, lectotype;
GLAM, isolectotype)].
Pseudoparmelia amazonica Parmelia caperata var. glaucopis Muller ilrgoviensis, 18943258
[type collection: Matangiri, Seen Region, Africa, Stuhlrnann
FIGURE6c 359 (559 o n type label) ( G , lectotype; BM, isolectotype)].
Parmelia glaucopis (Muller Argoviensis) Vainio, 1900:4.
Pseudoparmelia amazonica (Nylander) Hale, 1974: 189.
Parmelia subconspersa var. benguellensis Vainio in TVelwitsch,
Parrnelia amaronica Nylander, 1885:611 [type collection:
1901:401 [type collection: Mt. hlorro de Lopollo, Huilla,
Santarem, Brazil, Spruce 111 (H, Nylander herbarium n u m -
Angola, Welwitsclz 31 (BM, lectotype)].
ber 39111, lectotype; BM, G, NY, [V, PC, isolectotypes)].
Parmelia benguellensis (T'ainio) Dodge, 1959:70.
Pseudoparmelia benguellensis (Vainio) Hale, 1974:189.
DEscRIPTroN.-Thalhs closely adnate on bark,
5-10 cm broad, light mineral gray and turning buff DEscRiPTIoN.-Thallus rather closely adnate on
in the herbarium; lobes subirregular, apically ro- bark, coriaceous, greenish yellow, 3-5 cm broad;
tund, 2-6 mm wide, contiguous; upper surface lobes sublinear, crowded, partly black rimmed, 1-2
plane, continuous, moderately isidiate, the isidia mm wide; upper surface plane, dull, rugose and
rarely branched, to 2 mm high; lower surface black, becoming lobulate with age and heavily pycnidiate;
densely rhizinate except for a narrow naked or lower surface black and minutely velvety to the
papillate zone along the margins. Apothecia rare, margin, sparcely to moderately rhizinate. Apothecia
1-3 mm in diameter; spores 8, 8-10 X 13-16 pm. numerous, sessile, 1-2 mm in diameter; spores 8,
CHErvmmY.-Cortex K +
yellow, medulla K -, 7-8 X 16-18 pm.
+
C-, KC rose, Pf red; atranorin and protocetraric CHEMISTRY.-cOrteX K-, medulla K-, C-,
acid. KC-, or KC+ rose, P + red; usnic acid and proto-
DrsTR1BuTIoN.-United States (Florida), Central cetraric acid with or without a trace of atranorin.
America, West Indies, Colombia, Venezuela, Brazil, DIsTRisuTIo~.-Southern Africa.
Guinea, and Taiwan. HABITAT.-on trunks and branches of trees in
HABITAT.-& trees (conifers, palm trees, decid- open rocky areas.
uous trees), Opzintia, and on rocks in open forests REMARKS.-I had at first identified all African
at 100-1500 m elevation. specimens as Pseudoparmelia rutidota (Hooker and
REMARKs.-SUperficially this species could be con- Taylor) Hale, but close examination showed that
fused with P. salacinifera (Hale) Hale, which has a they have consistently narrow lobes and a jet black
pale brown lower surface and salazinic acid. T h e velvety lower surface (Figure la, b ) . By compari-
two occupy very similar habitats (trees in open son, P. rzitidota, which is known from Australia and
secondary forests) and geographic ranges. the New World, often has quite broad lobes (to
SPECIXIESS ExAxr1NED.-United States: Florida, Hale 34139, 5 mm wide) and a shiny surface below and brown
16859, 17668, 17696, Moore 3357 (DUKE, US), R a p p 311, 662 bare zone near the tips. T h e sorediate morph of
(US). Mexico: Veracruz, Hale 19389; Chiapas, Hale 19972 P . amplexa is P. subamplexa Hale and the isidiate
(DUKE, LD, US), Hale 20187 (Bhl, US), 20607a. Honduras: El
morph is P. pachydactyla (Hale) Hale. All three
Paraiso, Standley 560 (F): Morazan, S t a n d l e y and Williams
1643 (F). Cuba: Pinar del Rio, Imshaug 25289, 25310, 25333 appear to lack any fatty acids, in contrast to the
(MSC); Oriente, Hioram 5963 (US). Puerto Rico: H o w e 1162 P. rutidota group, which usually produces one or
(XU). Trinidad: Wedertnann 2305 (8). Colombia: Santander, more of the common fatty acids.
Killil, 15212, N e e and M o r i 3768 (US), Venezuela: Merida,
S a s h 2025 (US). Bolivia: El Beni, Wedernzann 2305 (S). Brazil: SPECIMENS ExAxr1mD.-Rhodesia: KoPer (LD, US), Schiitte
Minas Gerais, Vainio 588 (BM, T U R ) , 603 (BM, T U R ) ; Rio d e (LD, US), Sheppard 2 (US). Angola: Bie, Gossweiler 3256e
Janeiro Burchell 946 (BM); Mato Grosso, M a l m e s.n., 20506b (BM, US), Degelius (Degelius herbarium, US); Huila, De-
( S ) , 2369, 2408 (LD, S, US). Guinea: N'Zerekore, Santesson gelius (Degelius herbarium); hfoxico, Degelius (Degelius
10573a (UPS). Taiwan: Asahina (TNSL herbarium. US).
NUMBER 31 17
HABITAT.-on rocks in dry open areas at about species that will present much more detailed in-
1000 m elevation. formation.
REMARKS.-This rarely collected species seems to
REPRESENTATII E SPECI\IEhS EXAMINED (all in US).-Canada:
be related to P. annexa (Kurokawa) Hale, which Ontario, Hale. United States: Massachusetts, Hutchinson
contains lecanoric acid. T h e yellow pigmentation 1744; Connecticut, Hale 19076; New Jersey, Hale 17266;
does not seem to be a consistent character to judge Pennsylvania, Becking 57070315, Hale 16292, Heller, White
from the few specimens available. 210; Maryland, Hermann 13768, Leonard 2933, 3086, h'orden
27, Plitt; West Virginia, Hale 10734, 13016; Kentucky, Allen
SPECIMENS EXAXINED.-uniOn of South Africa: Basutoland, 545, Hale 13115; Illinois, Hale 13926, 14029, Skorepa 943;
KoPer (LD); Cape Province, Hiieg (TRH); Orange Free Wisconsin, Hale 23542, Thomson 919; Minnesota, Hale 23479;
State, Plank (PRE). Missouri, Greeninan 4763, Ireland 3238, Schoop 254; Virginia,
Hale 15107, 17317, Luttrell 120, 4876; Xorth Carolina, Cul-
berson in Lichenes Selecti Exsiccati 915, Hale 16371; Tennes-
Pseudoparmelia baltimorensis see, Degelius, Hale 31118, Phillips 321; South Carolina, Hale
7747; Georgia, Hale 30877; Alabama, Hale 7125, 33841, Mc-
FIGURE7b Cullough 344, 2032; Mississippi, Hale 7846; Arkansas, Hale
in Lichenes Ainericani Exsiccati 2, Hale 3644, 3813, Moore
259; South Dakota, Vischer 4; Kansas, Hale 2934, 4534; Okla-
Pseudoparmelia baltirnorensas (Gyelnik and Foriss) Hale,
1974:189. homa, Hale 5053; Texas, Hale 34317. A number of records
in other herbaria would have been identified as Parmelia
Parmelia baltimorensis Gyelnik and F6riss in Gyelnik, 1931a:
caperata by me before 1970; it was impractical to borrow
167 [type collection: Gunpowder RiFer, Baltimore County,
these specimens again and correct the names.
Maryland, Plitt (BP, holotype; US, isotype)].
Pseudoparmelia callichroa Kurokawa, new species Parmelia cuperata var. subglauca (Nylander i n Gasilien) Ny-
lander, 1896:35.
DESCRIPTIoN.-Thallus adnatus, ramulicola, Partnelia caperata f . laeuissima Gyelnik, 1928:587 [type col-
viridi-flavicans, 3-6 cm latus, lobis subirregularibus, lection: Meleghegy, Fehkr, Hungary, GyeInik (BP, holo-
congestis, apice subrotundatis; superne planus vel type)].
Pnrmelia herreana Zahlbruckner, 1929:239 [based on P. fiaui-
mox irregulariter rugosus, isidiis sorediisque desti- cans (Tuckerman) Tuckerman].
tutus; cortex superior 10-13 Fm crassus, epicortex Partnelia pseudosorediosa Gyelnik, 1931b:288 [based on Par-
perforatus, stratum gonidiale 12 pm crassum, me- nzelia ochroleuca f. sorediosa &fuller Argoviensis].
dulla alba, 100-120 pm crassa, cortex inferior 12-13 Parmelia negatiua Gyelnik 1934:301 [type collection: Salisbury
Cove, Maine, Plitt (BP, holotype)].
pm crassus; subtus niger, nitidus, modice rhizinosus, Pseudoparmelia euplecta (Stirton) Hale, 1974:190.
rhizinis simplicibus, nigris. Apothecia numerosa, Pseudoparmelia pseudosorediosa (Gyelnik) Hale, 1974:190.
amphithecio ruguloso, margine crenato, 1.O-4.5 mm
diametro; hymenium 70-85 pm altum; sporae 8:nae, DEscRIPTrox.-Thallus adnate to loosely attached,
6-8 X 13-16 pm. growing on bark or more rarely on rocks, yellowish
CHmmmY.-Cortex K -, medulla negative with green, 5-20 cm in diameter, coalescing to form
all reagents; usnic acid and protolichesterinic acid. larger colonies; lobes subirregular, apically rotund,
HoLoTYPE.-Chile: Colchagua, Hacienda de Con- 3-8 mm wide; upper surface plane to undulate or
quenes, P. Duse'n 91, 22 August 1896 (S; US, iso- rugulose, continuous, sorediate, the soralia laminal,
diffuse and coalescing; medulla rarely orange near
type).
DISTRIBUTIoN.-Chi~e. the lower cortex; lower surface black, moderately to
HABITAT.-On twigs. sparsely rhizinate except for a naked brown rugose
REMARKs.-This species would probably be zone along the margins. Apothecia very rare, 2-5
identified as P. rutidota (Hooker and Taylor) Hale mm in diameter; spores 8, 8-13 X 17-24 pm.
without a chemical test (P. rutidota is Pf red with CHESIISTRY.-COrteX K--, medulla K-, C-,
protocetraric acid). T h e thallus is smaller but we KC+ rose, Pf red, atranorin, caperatic, proto-
need many more collections to determine whether cetraric, and usnic acids; if pigmented, skyrin pres-
any morphological characters correlate with the ent.
chemical difference. DrsTRIsuTronl.-Pantemperate on all major conti-
nents (Figure 8).
HABITAT.-on conifers and deciduous trees in
Pseudoparmelia caperata temperate forests, common on rocks only at the
northern part of its range, from sea level t o over
7d
FIGURE 3000 m elevation.
RE&fARKs.-This is by far the most widespread
Pseudopartnelia caperata (L.) Hale, 1974:189.
Lichen caperatus L. 1753:1147 [type collection: England, and commonly collected foliose lichen in all tem-
Dillenius, Historia Muscoruin 193, specimen represented perate areas of the world. T h e range in morpho-
by $1. 25: fig. 97 (OXF, lectotype)]. logical variation is very small and the chemistry
Parmelia caperata (L.) Acharius, 1803:216. remarkably uniform. I n eastern North America it
Parmelia caperata b. cyliphora Acharius, 1814:196 [type col-
can be confused with the primarily saxicolous P.
lection: North America, Ltfulilenberg (H, lectotype; UPS,
isolectotype): listed in error as "cylisphora."] baltimorensis (see discussion above). T h e presump-
Parinelia perlata var. flauicans Tuckerman, 1866:13 [type tive nonsorediate parent seems to be P. rutidota
collection: California, flolaizder TO (FH-Tuck, holotype)]. (Hooker and Taylor) Hale (see below).
Parlnelia euplecta Stirton, 1877-78:299 [type collection: Bris- Older authors consistently placed this species in
bane, .4ustralia, Bailey (BM,lectotype)]. Parmelia section A m p h i g y m n i a (= Parmotrema).
Parnielia flauicans (Tuckerman) Tuckerman, 1882:53 [not
P . flauicans (Swartz) Acharius, 1803:268 (= Teloschistes)].
T h e lobes, however, are clearly adnate at the mar-
Partnelia o c h r o l e w a f . sorediosa Muller Argoviensis, 1883b: gins, the bare rim below is very narrow, the tips of
77 [type collection: Mt. Dromedary, Australia, Reader (G, rhizines near the margin are frayed, and the apo-
lectotype)]. thecia are adnate and nonperforate. This combina-
Parmelia subglauca Nylander in Gasilien, 1894:126 [type tion of characters relates the species much m6re
collection: Saint Omer, France (H, lectotype: BM, PC iso-
closely to Pseudoparmelia than to Parmotrema.
types)].
Parmelia cylisphora [sic] (Acharius) Vainio, 1896b:7. T h e species is apparently present in Australia
NUMBER 31 21
FIGURE
8.-World distribution of Pseudoparmelia caperata. (Dots may represent more than one
collection.)
and New Zealand, represented by the anonomously regularly sublinear, often densely imbricate, 3-6
pustulate P. euplecta. Parmelia ochroleuca f . sore- mm wide; upper surface plane or rugulose, cracked
diosa, also described from Australia, is atypical in with age; lower surface black, moderately rhizinate.
having rather discrete orbicular soralia. Future Apothecia subpedicellate, at first globose, urceolate
studies in this region may show that these popula- at maturity, u p to 5 mm in diameter; spores 8, 4-5
tions are distinct from P. caperata. X 10-13 pm.
SPECIMENS EXAMINED.-%e Figure 8 for localities of speci-
CHEMISTRY.-cOrteX K + yellow, medulla K--,
mens annotated in the major herbaria. Some specimens from + +
C -, KC rose, P red; atranorin and protocetraric
eastern North America which I annotated before about 1972, acid.
especially those on rock, will be P. baltimorensis. DISTRIBUTION.-weSt Indies and French Guiana.
HABITAT.-oII schist and volcanic rocks in open
areas u p to 275 m elevation.
Pseudoparmelia caribaea REMARKS.-Except for the t w o specimens from
FIGURE7e French Guiana and the Isle of Pines, P. caribaea
is confined to St. Barthblemy, where it has been col-
Pseudoparmelia caribaea (Hale) Hale, 1974:189. lected many times. There are n o close relatives in
Parmelia caribaea Hale in Hale and Kurokawa, 1964:152 the genus.
[type collection: St. Barthdemy, West Indies, L e Gallo 494
(US, holotype)]. SPECIMENS EXAMINED.-cUbP: Isle of Pines, Rritton et al.
14436, 15237 (US). St. Barthelemy: Le Gallo 403, 424, 527,
DEscRxPTIoN.-Thahs adnate on rocks, ashy 536, 546 (US), 2604 (MSC, US). French Guyana: Degelius
white, rather coriaceous, 6-10 cm broad; lobes ir- (Degelius herbarium).
22 SMITHSONIAN COXTRIBUTIONS T O BOTANY
Pseudoparmelia carneopruinata South Carolina, Ravenel 404 (H, lectotype; FH-Tuck, iso-
lectotype)].
FIGURE7 f Parrnelia perlata var. subrevoluta Miiller Argoviensis, 1880:267
Pseudoparrrielia carneopruinata (Zahlbruckner) Hale, 1974: [type collection: Petropolis, Brazil, Deventer 45 ( G , lecto-
189. type)].
Parmelia carneopruinata Zahlbruckner, 1902:419 [type col- Parmelia isidiophora Zahlbruckner, 1902:420 [type collection:
lection: R i o d e Janeiro, Brazil, HBhnel 164 (W,lectotype)]. Botanical Garden, Rio d e Janeiro, Brazil, Hohnel 169, (W,
Parrnelia sbnrbaronis Bouly de Lesdain, 1923:278 [type col- lectotype)].
lection: Catalupe, Varezze, Liguria, Italy, Gresino 11467 (F, Partnelia luteola Zahlbruckner, 1909:170 [type collection:
lectotype)] . S e a r Barra Mansa, SPo Paulo, Brazil, Wettstein and Schifl-
iier (W, lectotype)].
DEsCRIPTIor\;.-Thallus closely adnate, corti- Parinelin zuainoana Lynge, 1914:87 [type collection: Santa
colous, greenish mineral gray or in the herbarium Anna da Chapada, Mato Grosso, Brazil, Malme 2435C (S,
buff, 5-9 cm in diameter; lobes sublinear, 1-2.5 m m lectotype)].
wide; upper surface strongly reticulately ridged and Pyxine azorea Nylander, 1895:lOO [type collection: Azores,
rugulose, becoming pruinose near the lobe tips, Michel 66 (H, lectotype)].
sometimes densely lobulate, sorediate, soralia about
DEsCRIPTION.-Thal~us closely adnate to bark,
1 mm wide, often coalescing; lower surface black,
rarely on rock, 5-10 cm broad; lobes subirregular,
sparsely rhizinate. Apothecia rare, adnate, 1-4 mm
rotund, 2-5 mm wide; upper surface plane, re-
i n diameter, the disc pruinose or naked, the am-
ticulately white-maculate and finely cracked, densely
phithecium sorediate; spores 8, 6-9 X 9-1 3 pm.
isidiate, the isidia 1-3 mm high, often branched;
CHEMISTRY.-cOrteX K +
yellow, medulla K f
lower surface black, very rarely uniformly dark
yellow, C-, KC-, P f pale orange; atranorin,
brown, moderately rhizinate except for a narrow
stictic acid, and constictic acid with associated un-
naked or papillate zone along the margins. Apo-
knowns.
thecia rare, adnate, 1-3 mm in diameter, the am-
DIsTRIBuTIoN.-h!feXiCo, Central America, West
phithecium isidiate; spores 8, 6-8 X 13-15 pm.
Indies, Colombia, Venezuela, Brazil, Uruguay, Ar-
gentina, and southern Europe.
CHEMISTRY.-cOTteX K +
yellow, medulla K -,
HABITAT.-on shade trees in banana and Coffee
+
C -, KC faint rose or purple, P - ; atranorin and
perlatolic acid with associated unknowns.
plantations and on deciduous trees in open pastures
DIsmrnuTroN.-Southeastern United States,
at 300-2000 m elevation.
Mexico, Central America, West Indies, Venezuela,
REbfARKs.-This species is closely related to P.
Ecuador, Brazil, Azores, Africa, and Thailand.
scrobicularis (Krempelhuber) Hale, which is or at HABITAT.-on trees (conifers and deciduous
least may be the nonsorediate progenitor. Another trees) in coffee plantations, secondary forest, and
very close sorediate species, P. crozalsiana (Bouly de pastures and rarely on rocks from sea level t o 2800
Lesdain) Hale, has much broader, subrotund lobes m elevation.
and a wider, more temperate distribution. T h e two RE&aARKs.-The first study of this species was
species, however, probably intergrade and are not
done by Culberson (1957), who clarified its re-
always easily distinguished. lation and frequent confusion with Parmelia
SPECIMENS ExAhrr?iEo.-Mexico: Xayarit, W e b e r 33609 rudecta Acharius, another widespread species which
(COLO); Veracruz, Hale 19398, 19432 (DUKE, US), 19452,
differs in having pseudocyphellae and lecanoric acid
19654, 19672, 19794, 21081, 21195. Honduras: Morazln,
Standley 11655 (F, US), 11657 (F). Costa Rica: San Josk, as well as a paraplectenchymatous upper cortex.
Standley 34811 (US). Jamaica: Orcutt 5603 (US), Plitt (Us). Pseudoparmelia caroliniana is the only isidiate spe-
Colombia: Lindig 2590 (G). Venezuela: Mkrida, Hale 42785, cies in the genus with perlatolic acid; P. aptata
42912. Brazil: Minas Gerais, M e x i a 5322 (BM); SPo Paulo, (Krempelhuber) Hale also has perlatolic acid but
Schindler 4512, 4525 (KR, US). Uruguay: Canelones, Osorio is sorediate and lacks the fine reticulation so charac-
6236 (MVM). Argentina: Jujuy, Fries 43b (S). Europe: Italy,
Sbarbaro (TUR). teristic of P. caroliniana. I wish to thank Dr. T. D.
V. Swinscow for pointing out the synoymy of
Pseudoparmelia caroliniana Pyxine azorea.
FIGURE9a SPEcrarENs ExAMrNm.-United States: See Culberson (1957)
Pseudoparmelia caroliniana (Nylander) Hale, 1974: 189. for localities over the range in the United States a n d Moore
Parmelia caroliniana Nylander, 1885:614 [type collection: (1968:223) for specimens from Florida. Mexico: Hidalgo,
NUMBllR 31 23
Robinson (US); Veracruz, Hale 19471, 19488, 21131, 21135; DEscRIPTIoN.-Thallus adnate, fragile, ashy
Chiapas, Hale 19900, 20104, 20144, 20215, 21310, 20333. Hon- eral gray, 4-5 cm broad; lobes short, beco
duras: MoraaBn, Standley 238, 11603 (F). Nicaragua: Standley
imbricate, 1-3 mm wide; upper surface plane
8432 (F). Costa Rica: Guanacaste, Standley 44370 (US).
Panama: Chiriqdi, Hale 38804. Cuba: W r i g h t 71 (FH, M, PC, regularly cracked with age, densely isidiate, i
UPS, US); Oriente, Imshaug 24763, 24858 (MSC). Jamaica: . cylindrical, simple or branched; lower surface b
I m s h a u g 13762, 14200 (MSC), Plitt (US). Haiti: Ouest, I m s h a u g rhizines moderate to sparse. Apothecia abun
22542, 22859, 22944, 23061 (MSC, US), Wetmore 2882, 3076, adnate; spores 8, 6 X 12 pm.
3149, 3207 (MSC, US), Leonard 3709b (US). Dominican Re-
CHEMISTRY.-cOrteX K f yellow, medulla
public: Cordillera Central, Imshaug 23714 (MSC, US, WIS),
23718 (Bhf, G, MSC); La Vega, Allard 18033 (US). Venezuela: yellow turning red, C-, KC-, P + orange
Distrito Federal, Dennis 1503 (BM). Santesson 6672, 6681 (S); ranorin and salazinic acid.
Mbrida, Hale 42039, 42196, 43318, 44081, 44225; Tachira, DIsTRIBunoN.-Brazil and Paraguay.
Hale 45632, 45649. Ecuador: Galapagos, Johannsen 10 (WIS), HABITAT.-On trees in open forest.
Weber 40031 (COLO, UPS). Brazil: Rio de Janeiro, Eiten
REMARKS.-This rare species is superficially
7373 (US); SaoPaulo, Eiten 2978, (US) Osorio 4925 (MVM);
Santa Catarina, Reitz and Klein 13145, 15398 (US). Europe: P. salacinifera (Hale) Hale, which differs in ha
Portugal, Persson (UPS). Ivory Coast: Man, Santesson 10494 a pale brown lower surface.
(UPS, US). Uganda: Burahiya County, Swinscow 2U 18 (BM); SPECIMESSExAI\fINED.-Brazi1: Pernambuco, Xavier 713
Kyadondo County, Swinscou! 2U 1 / 7 (BM). Angola: Huila,
Degelius (Degelius herbarium). Laos: T s u y a m a 19 (TNS). Pseudoparmelia concomitans, new species
FIGURE9d
Pseudoparmelia chapadensis
FIGURE9b
DEscRIPTIoN.-Thallus laxe adnatus, cort
bubalino-albidus, coriaceus, 4-6 cm latus, lobis
Pseudoparmelia chapadensis (Lynge) Hale, 1974:189. irregularibus, apice rotundatis, 3-5 mm
Parmelia chapadensis L ~ n g e ,1914:153 [t) pe collection: near
Bocca da Serra, Serra da Chapada, Mato Grosso, Brazil,
superne planus, nitidus albo-maculatusque, so
Malme 2297B (S, lectotjpe)]. et isidiis destitutus; cortex superior 10-14 pm
sus, epicortex sparse perforatus, stratum goni
DEscRIPTIoN.-Thallus closely adnate on rock, 10-12 pm crassum, medulla 90-110 pm c
yellowish green, 1-1.5 cm broad; lobes sublinear, Cortex inferior 8-10 pm crassus; subtus n
short, 0.5 mm wide, convex and expanded at the sparse rhizinosus, ambitu nudus, castaneus, nit
tips; medulla yellowish; lower surface pale brown, Apothecia numerosa, substipitata, 1-2 mm
moderately rhizinate. Apothecia common, sessile, metro; sporae 8:nae, 12 X 20-23 pm.
0.5-1.0 mm in diameter; spores 8, 4-5 X 8-10 p.m. CHEMISTRY.-cOrteX K +
yellow, medulla
CHEMISTRY.-cOrteX K -k yellow, medulla K f ,
C + , KC+ yellowish, P + red; unidentified sub-
C +, + +
KC red, P red, atranorin, gyrophoric
and protocetraric acid.
stances present. HoLoTYPE.-New Caledonia: Baie des Crabe
DIsTRIBuTION.-Brazil. de Pins, on fallen branches of Araucaria cookii,
HABITAT.-Rocks in open areas. Hill 12124 (BM; US, isotype) .
REMARKS.-This peculiar species is tentatively DISTRIBUTION.-New Caledonia.
placed in Pseudoparmelia because the lobes are HABITAT.-on branches of Araucaria.
eciliate and the rhizines simple. Contrary to my REMARKS.-This species is known only from
earlier findings (Hale, 1960), it does not contain type collection and seems unrelated to any
usnic acid or protocetraric acid. T h e yellow colora- Pseudoparmeliae. T h e lobes are coriaceous
tion is caused by unidentified pigments in both the strongly white maculate. Only P. martinicana
cortex and the medulla. Perhaps additional collec- duces this combination of medullary substance
tions will clarify the status of the species. it is an isidiate, fragile lichen confined to the
Indies.
Pseudoparmelia cinerascens
FIGURE
9c Pseudoparmelia concrescens
FIGURE9e
Pseudoparmelia ciwrascens (Lynge) Hale, 1974:189.
Parmelia cinerascens Lynge, 1914:104 [type collection: Para- Pseudoparmelia concrescens (Vainio) Hale
guari, Paraguay, Afalme 1498 (S, lectotype)]. Parmelia concrescens Vainio, 1901:400 [type collection:
NUMBER 31 25
da Xella, Huila, Angola, Welwitsch 30 pro parte (TUR, bullate, the cortex breaking away easily; lower sur-
lectotype; BM, isolectotype)]. face pale brown, moderately rhizinate, the rhizines
Parmelia capensis Nylander, 1885:613 [type collection: Cape pale. Apothecia numerous, adnate, 1-2 mm i n di-
of Good Hope, Union of South Africa, Drege (H, Nylander
herbarium number 35174, lectotype; PC, isotype); not ameter; spores 8, 4 X 5 pm.
P. capensis (Acharius) Sprengel, 1827:280 (= Teloschistes)]. CHEMISTRY.-cOrteX K f yellow, medulla Kf
Parmelia austroafricana Zahlbruckner, 1929:152 [type: based yellow turning red, C-, KC-, Pf orange; atra-
on P. capensis Nylander]. norin, chalybeizans unknown, salazinic acid, and
Parmelia caffrorum Zahlbruckner, 1932a:555 [type: based on a pale yellow unidentified pigment.
P . capensis Nylander].
DISTRIBUTION.-~outh Africa.
DEscRwTIoN.-Thallus adnate o n bark, ashy HABITAT.-On rocks in open dry areas.
mineral gray, 4-10 cm in diameter; lobes irregularly REMARKS.-This is another species of Pseudopar-
sublinear, 1-3 mm wide; upper surface plane, con- melia that bears a close resemblance to Xanthopar-
tinuous or cracked on older lobes, densely isidiate, melia. T h e chalybeizans unknown, in fact, was
the isidia short, cylindrical, mostly simple; lower previously known only in Xanthoparmelia (Hale,
surface black, sparsely rhizinate. Apothecia rare, 1972b). This specimen apparently endemic to the
adnate, 2-3 mm in diameter; spores 8, 5 X 7-8 pm. arid regions of South Africa.
CHEMISTRY.-cOrteX K +
yellow, medulla K - , SPECIMENSExAhrlNED.-Material from the Union of South
C--, KCf faint wine red, P-; atranorin and di- Africa is listed in Hale (1972b3343).
varicatic acid with associated unknowns.
DISTRIBUTION.-SOUthern Africa. Pseudoparmelia conlabrosa, new species
HABITAT.-On trees or rocks in open woodland
FIGURE10a
at 1000-2300 m elevation.
REMARKS.-ThiS is one of the commoner, more DEscRIPTIoN.-Thallus arcte adnatus, corticola,
widespread lichens in Africa. I t is presumed to be viridi-albidus, 3-5 cm latus, lobis sublinearibus,
an isidiate morph of P. nairobiensis (Steiner and apice plus minusve subrotundatis, congestis, 2-2.5
Zahlbruckner) Hale, with which it is sympatric. m m latis; superne undulatus, nitidus, apice albo-
I t is also close to the more widespread P. ecaperata reticulatus, dense isidiatus, isidiis cylindricis, pro
(Muller Argoviensis) Hale, which differs i n con- maxima parte simplicibus, usque ad 0.5 mm altis;
taining usnic acid in the cortex. cortex superior 10-12 pm crassus, epicorticatus, epi-
SPECIMENS ExA%rINED.-uganda: Dummer 602 (US); Busiro cortice perforato, stratum gonidiale ca 10 pm
County, Swinscou! 2U 24/21 (BM, US); Kinkizi County, Dale crassum, medulla alba, ca 100 pm crassa, cortex in-
L46 (BM, US). Zaire (Congo): Degelius (Degelius herbarium, ferior paraplectenchymatus, 8-10 pm crassus; subtus
US), Hoeg (TRH), Louis 7494 (BR), de Witte 2675 (BR). niger, modice rhizinosus, rhizinis nigris, simplici-
Angola: Cuanza-Sul, Degelius; Bie, Degelius; Huila, Degelius;
Moxico, Degelius (all Degelius herbarium). Rhodesia: Arne11
bus. Apothecia ignota.
1282a (LD), Schutte 46c (LD, US). Moqambique: Alrnborn CHEMISTRY.-cOrteX K + yellow, medulla K -,
6888, 7015 (LD). Union of South Africa: Natal, Almborn C +, +
KC red, P - ; atranorin and lecanoric acid.
8637 (LD). HoLoTYPE.-Australia: New South Wales, be-
tween Majors Creek and Araluen, W e b e r and
M c V e a n L-47102, 18 October 1967 (US; COLO,
Pseudoparmelia condyloides isotype).
FIGURE9f REMARKs.-This species is obviously related to
Pseudoparmelia labrosa (Zahlbruckner) Hale, a
Pseudoparmelia condyloides (Kurokawa) Hale, 1974:189. sorediate species with lecanoric acid also known
Parmelia condyloides Kurokawa in Hale, 1972:343 [type col-
lection: Kamieskroon, hamaqualand, Union of South
from Australia. N o parent morph has yet been dis-
Africa, Almborn 4882 (LD, holotype; TNS, US, isotypes)]. covered for these two species.
DESCRIPTIoN.-Thallus closely adnate on twigs, Hale, a ciliate species. Since then it has been recog-
whitish mineral gray, about 6 cm broad; lobes nized from many localities. T h e lobes are usually
irregularly elongate, apically rotund, 1.5-3 mm quite broad and apically subrotund and the reticu-
wide; upper surface rugulose; medulla white in the late wrinkles very distinct without magnification.
upper part and deep yellow in the lower half; lower Once the chemistry is recognized, it could only be
surface black, sparsely rhizinate. Apothecia numer- confused with Parmelia carneopruinata (see be-
ous, 1-4 mm in diameter; spores 8, 7 X 10 pm. low), which has lobes less than half as wide on
CHEMIsTRY.-Cortex K +yellow, medulla nega- the average. There seems to be n o nonsorediate
tive with color reagents except for the pigment progenitor extant, unless we consider it to be the
which is K + purple, atranorin, and unidentified rare African species P. inhaminensis (Dodge) Hale.
substances. When I first examined the surface of this species
DISTRIBUTION.-~outh Australia. with the scanning-electron microscope (Hale,
HABITAT.-on twigs of tree in open area. 1973a), I noted a strongly nodular surface without
REMARKs.-ThiS species is very similar to P . pores, an anamolous condition for the genus. How-
subtiliacea (Nylander) Hale, which differs in hav- ever, examination of other species has shown that
ing a white medulla without pigments but with pores do occur rarely but that even though the
fatty acids. One additional specimen, which I have species does not seem to have a paraplectenchy-
not seen, was collected by Rogers (95) in Para- matus upper cortex, as one would expect in a
Wirra national Park, South Australia. T h e species nonepicorticate Parmelia, the cortical structure of
is well illustrated in Kurokawa and Filson (1975) this species is rather atypical.
(PI. 1: fig. 3). SPECIMENS EXAnfINED.-United States: Illinois, Hale 13980,
Skorepa 1757 (US); Indiana, Hale 14097; Kentucky, Hale
Pseudoparrnelia crozalsiana 13691; Ohio, Hale 13576; Virginia, Hale 15232, 15761, 18455;
Arkansas, Keck 1216 (US): Alabama, Hale 33829. Mexico:
FIGURE10b Mexico, Hinton 7724 bis (BM); Veracruz, Hale 19494. Venez-
uela: Merida, Hale 42288, 42312, 43049a: Tachira, Hale
Pseudoparmelia crozalsiana (Bouly de Lesdain) Hale, 1974: 45704. Brazil: Mato Grosso, Malme 2243C (S); Parana, Montes
189. 10121 (DUKE); Pernambuco, Xavier 700 (US). Uruguay:
Parmelia crozalsiana Bouly de Lesdain ex Harmand, 1909: Lavalleja, Osorio 3667 (DUKE); Maldonado, Osorio 4879
555 [type collection: Agde, Herault, France, D e Crozals, (US): Rivera, Osorio 1075 (US). Argentina: Tucumain, Ven-
May 1909 (US, lectotype)]. turi 336 (DAR). Europe: Italy, Davies (BM), Sbarbaro (US),
Sbarbaro in Lichenotheca Pama 32 (M), Sbarbaro in Lichenes
DESCRIPTIoN.-Thalhs adnate to bark, greenish Selecti Exsiccati 96 (H, LD, US). Uganda: Mawakota County,
mineral gray, 5-10 cm broad; lobes subirregular, 3-6 Swinscow 2U 41/2 (BM, US). Zaire: Louis 8150 (BR). Union
mm wide; upper surface strongly reticulately ridged of South Africa: Natal, Almborn 8636 (LD), Hoeg (TRH).
India: Tamil Nadu, Awasthi 4276 (Awasthi herbarium), Hale
and wrinkled, sometimes white-pruinose, sorediate, 43976.
the soralia often produced along the ridges, coa-
lescing; lower surface black, moderately rhizinate
except for a narrow brown marginal zone. Apo- Pseudoparmelia cyptochlorophaea
thecia not seen. FIGURE10c
CHEMISTRY.-cortex K +yellow, medulla K $.
yellow, C-, KC-, P f pale orange, atranorin, Pseudoparinelia cryptochlorophaea (Hale) Hale, 1974: 189.
stictic acid, constictic acid, and associated un- Parinelia cryptochlorophaea Hale, 1959: 18 [type collection:
Ciudad Trujillo, Dominican Republic, Allard 15715a (US,
knowns. holotype)].
DIsTRIBuTroN.-Eastern United States, Mexico,
Brazil, Uruguay, Argentina, France, Italy, Zaire, DESCRIPTION.-Thal~Us adnate to appressed on
Union of South Africa, and India. large branches, 5-10 cm in diameter, light mineral
HABITAT.-on trees in open secondary forests gray but soon turning buff in the herbarium; lobes
at 100-2000 m elevation. 3-5 mm wide, apically subrotund, crowded; upper
REMARKS.-I first identified this species in North surface rugulose and shiny, more or less reticulate
America in 1960 (Hale, 1960) where it had been white-madate at the tips, becoming cracked in
misidentified as Parmelina aurulenta (Tuckerman) older parts; margins sorediate, the soredia in dense
28 ShlITHSONIAN C O N T R I B U T I O S S T O BOT.4NY
erect soralia, 0.6-1.0 mm thick, 1-1.5 mm high: HABITAT.-On trunks of trees in forest.
lower surface black and rhizinate at the center, REMARKs.-This species is clearly the isidiate
brown and naked to papillose in a narrow zone at morph of P. sphaeyospora (Nylander) Hale. Un-
the margins. Apothecia rare, 1-3 mm in diameter, fortunately it is still known only from the type
spores 8, 4-5 X 6-9 pm. locality.
CHEMISTRY.-cOrteX Kf yellow, medulla K-,
C-, KCS. rose, P-; atranorin, caperatic acid (C. Pseudoparmelia dahlii, new species
Culberson, 1965) , and cryptochlorophaeic acid.
DISTRIBUTION.-SOUtherrI United States, ~ ~ e x i c o , FIGURE10e
Central America, Tt7est Indies, Venezuela, and Thallus adnatus, corticola, viridi-flavicans, 3-4
Brazil.
cm latus, lobis sublinearibus, contiguis, 1.5-2.0
HABITAT.-OII trees (cashew, X y l o p i a , bamboo,
mm latis; superne convexus, opacus, dense isidiatus,
etc.) in mature forests at sea level to 500 m eleva-
isidiis cylindricis, simplicibus, usque ad 0.5 mm altis;
tion.
cortex superior 12-14 pm crassus, epicorticatus;
RE&fARKS.-The most unusual feature of this
stratum gonidiale 15-20 pm crassum; medulla alba,
New Tliorld species is the chemistry, the only re- 140-160 pm crassa; cortex inferior paraplectenchy-
ported occurrence of cryptochlorophaeic acid in the
matus, 12-14 p ~ crassus;
i subtus pallide castaneus,
Parmeliaceae. T h e capitate soralia are also unique. dense rhizinosus, rhizinis pallidis, simplicibus, elon-
T h e white reticulation is similar to that in the gatis. Apothecia adnata, 1 mm diametro: hymenium
Parinelia texana group, with which it is obviously 40-45 pm altum; sporae S:nae, 6 X 7-9 pm.
closely allied. CHEhfISTRY.-cOrteX K -, medulla K-, c +,
SPECIXIESS ExAarIxED.-United States: Georgia, Hale 16797, KC+ red, P-, usnic acid, caperatic acid and le-
21985; Florida, Hale 16989, 17584, 17609, 21674, 21815, 21839, canoric acid.
R a p p (US) (for furthcr records from Florida in DUKE see HoLoTYPE.-sri Lanka: Polonnaruwa, E . Dahl, 6
Moore, 19683225). Slexico: \eracruz, Hale 19771, 19811. H o n -
duras: Comayagua, Standley 5462, 5930 (F). Jamaica: Imshaug January 1972 (0;US isotype).
15967, 15969 (US), Plitt s.n. (US). Dominican Republic: La DISTRIBUTION.-.!%iLanka.
Vega, Allard 16833, 16845, 16834, 16861, 18028; Santiago, HABITAT.-On trees in lowland forest.
Znishaug 23884 (XISC, US); Santo Domingo, Allard 15715, RE~rARKs.-Superficially this lichen resembles P.
16182, 16187, 16191a (US). Trinidad: Degelius s.n. (Degelius malaccensis (Nylander) Hale yery closely, but the
herbarium); Lassen (C); Lewis 347 (PH). Venezuela: Barinas,
Steyerniark and R u b e 96533 (US); Mkrida, Hale 42305a.
rhizines are denser and longer, the lobes thicker
Brazil: Ceara, Cutler 8072c (F); Rio de Janeiro, Glaziou 1848 and dull without alboreticulate patterning, and
(M). the chemical components different. It is, however,
clearly a member of the P. intertexta-P. malaccensis
lowland rain forest complex. Another closely related
Pseudoparmelia cyphellata species, P. rakengensis (Vainio) Hale, which occurs
FICCRE 10d in the higher elevation monsoon forest in Thailand,
is also externally very close. Chemical tests are
Pseudopnrmelm c ) p h e l [ a t a Llnge, 1914.15 [type collection. needed to identify the species. I wish to thank Dr.
Santa Anna da Chapada, Mato Grosso, Brazil, 21\lnln2e
Hildur Krog for allowing me to see the specimens
2532B (S, 1ectot)pe; LD, UPS, CS, isolectot)pes)]
Parnzelra cTphellata (Lynge) Santesson, 1942.473. and to describe them.
SPECI\fENS EXA\rlhED.-sri Lanka: Dambulla, DahZ (0,us).
DEsCRIPTIoN.-Thallus as in P. sphaerospora (see
below) except the upper surface isidiate, isidia
cylindrical, rather sparse, u p to 1 mm tall. Apo- Pseudoparmelia ecaperata
thecia abundant, adnate to substipitate, 2-3 m m FIGUREl O f
in diameter; spores 8, about 5 X 7 pm.
Pseudoparrnelia ecapernta (Muller Argoviensis) Hale, 1974:
CHEhlISTRY.-cOrteX K f yellowish, medulla yel-
190.
lowish to orange with color reagents; atranorin, Parrnelia acaperata Muller Argoviensis, 1891:378 [type col-
stictic acid, and an unidentified pigment. lection: Shire River, Zambesica, Africa, Kirk (G, lecto-
DIsTRIsuTIoN.-Brazil. type; BM, isolectotype)].
NUMBER 31 29
Parmelia nialaccensis var. laetepavens Vainio, 1921:38 [type- orbicular, confluent with age; lower surface black,
collection: Doi Sutep, Thailand, Hosseus, 1904 (TUR, moderately rhizinate. Apothecia unknown.
Vainio herbarium number 2764, lectotype)]. CHEMISTRY.-cortex K 4- yellow, medulla K - ,
Parmelia laetepavens (Vainio) Gyelnik, 1938a:32.
Parmelia djalonensis des Abbayes, 1951:966 [type collection: C-, KC-, P + red; atranorin and protocetraric
Fouta-Djalon, Dalaba, Guinea, des Abbayes (REN, lecto- acid.
type)] DIsTRIBuTI0N.-Kenya and Mocambique.
HABITAT.-On coconut and other trees in open
DEScRIPTIoN.-Tha1Ius as in P. concrescens (see
forest or savanna u p to 300 m elevation.
above) except yellowish green. Apothecia rare, 1-4
REMARKS.-This rare lichen appears to be the
mm in diameter, the amphithecium isidiate; spores
sorediate morph of P. schelpei (Hale) Hale, which
8, 6 X 11-14 .pm.
also occurs in Mocambique. T w o superficially re-
CHEMISTRY.-cOrteX K--, medulla K--, c - ,
lated sorediate species with protocetraric acid occur
KC+ faint wine red, P-; atranorin, divaricatic
in the New World: P. alabamensis (Hale and Mc-
acid, and usnic acid, rarely with protolichesterinic
Cullough) Hale, which is saxicolous and has gen-
acid.
erally narrower lobes, and P. raukiaeri (Vainio)
DISTRIBUTION.-Africa, Nepal, India, and Thai-
Hale, which has irregular pustular soredia.
land.
HABITAT.-On trees or more rarely rocks in open SPECIMENSExAxfINED.-Kenya: Coast Province, Santesson
forest u p to 2000 m elevation. 20898 (UPS, US), Mocambique: Sul d o Save, Schelpe 4461a
(BOL, US), 4460a, 4461b (BOL).
REMARKs.-This species represents the isidiate
morph of P. zambiensis (Hale) Hale. It also repre-
sents the usnic acid-containing counterpart of P . Pseudoparmelia eruptens
concrescens, a species which does not occur outside FIGUREl l b
of Africa. It has no relationship to P. caperata, as
the name might be construed to imply, which con- Pseudoparmelia eruptens (Kurokawa) Hale, 1974:190.
tains protocetraric acid. Parmelia eruptens Kurokawa i n Hale and Kurokawa, 1964:
153 [type collection: Lydenburg, Transiaal, Union of South
SPECIMENS EXAI\lINED.-IVOry Coast: Seguela, Santesson Africa, A l m born 7498 (LD, holotype; US, isotype)].
10698a, 10702b (UPS, US). Guinea: NZerekore, Santesson
10568a (UPS, US). Zaire: Hoeg (TRH), Schmitt 3048 (BR). DESCRIPTION.-Tha11us adnate, corticolous, whit-
Angola: Bie, Degelius (Degelius herbarium); Cuanza Sul, ish mineral gray to buff in the herbarium, 5-8 cm
Degelius (Degelius herbarium); Huila, Degelius (Degelius broad; lobes subirregular, rotund, 2-8 mm wide;
herbarium); Moxico, Degelius (Degelius herbarium). Rho- upper surface plane, continuous, moderately isidiate-
desia: Angus (BM), Hoeg ( T R H ) , Kofler (LD), Schutte 61b
(LD, US). hfalawi: Jellicoe 55 (BM). Nepal: Poelt 107, 114
pustulate, the isidia irregularly inflated, basally
(M, US), Noordyte (L), Togashi (TNS). India: Tamil Nadu, constricted, bursting apically; lower surface black,
Awasthi 4431, 4432 (Awasthi herbarium, US), Degelius As- sparsely rhizinate except for a narrow naked zone
256 (Degelius herbarium), Foreau 54 (Awasthi herbarium, at the tips. Apothecia rare, adnate, 1-3 mm in
US), Hale 43673, 43713, 43866, 43948; Uttar Pradesh, Awasthi diameter, the amphithecium coarsely isidiate; spores
3496, 3972 (Awasthi herbarium). Thailand: Kurokawa 1670,
1954 (TNS, US), Tsuyama (TNS, US).
8, 5-7 X 19-12 pm.
CHEMISTRY.-COrteX K + yellow, medulla K - ,
C-, KC- or KC+ purple violet, P-; atranorin
Pseudoparmelia epileuca and divaricatic acid with associated unknowns.
DIsTRIBUTIoN.-Mocambique and Union of South
FIGUREI l a
Africa.
Pseudoparmelia epileuca (Hale) Hale, 1974:190. HABITAT.-on trees (and rocks?) in open forest.
Parmelia epileuca Hale, 1972:343 [type collection: District REMARKS.-This rare species is probably most
Inhambane, MoGambique, Schelpe 4461 (BOL, holotype;
isotypes in LD, US)].
closely related to sorediate P. texana (Tuckerman)
Hale. T h e large pustules of P. eruptens do not be-
DEscRIPTIoNs.-Thallus closely adnate on bark, come sorediate.
ashy white, 3-5 cm broad; lobes sublinear, contigu- SPECIMENS ExAM1NED.-Mocambique: Mitchell 332 (us).
ous, with smooth dark rimmed margins, 1.5-2.0 mm Union pf South Africa: Transvaal, hlaas Geesteranus 6453
wide; upper surface plane, sorediate, the soralia (L, US), 6455 (L).
SMITHSONIAN CONTRIBUTIONS T O BOTANT
* I a'"-
FIGURE11.-Species of Pseudoparvielin: a, P. epileuca (Schelpe 4461b, isotype in BOL); b, P.
eruptens ( A l m b o r n i498, holotype in LD); c, P . exoriiata (Lamb 1101 in US); d, P. ferax (Rogers
1326 in US); e, P. geesterani (Maas Geesteranus 6405, holotype in L); f , P. gerlachei (Santesson
6499 in US). (Scale in mm.)
NUMBER 31 31
Pseudoparntelia exornata, new combination Parmelia citrinescens Gyelnik, 1938b:271 [type collection:
Lago Nahuel, Puerto Blest, Patagonia, Argentina, Duste
FIGUREl l c 163 (BP, holotype; S, US, isotypes)].
Parmelia caperata var. exornata Zahlhruckner, 1912:379 [type DEScRIPTIoN.-Thallus closely adnate on bark,
collection: Cerillos Canelones, Uruguay, Felippone 431 (W, greenish yellow, 5-8 cm broad; lobes subirregular,
lectotype; G, isolectotype)]. crowded, apically rotund, 3-4 mm wide; upper sur-
Parmelia rutidota f. filizans Lynge, 1914:153 [type collection:
Quinta, Rio Grande do Sul, Brazil, M a l m e 727 (S, lecto- face soon wrinkled and rugose, in part warty and
type)]. lobulate; lower surface black and coarsely rhizinate
except for a narrow brown zone at the margins.
DEsCRIPTIoN.-Thallus adnate to closely adnate Apothecia common, sessile, plane to almost urceo-
on bark, yellowish green, 4-10 cm broad; lobes sub- late, 2-4 mm in diameter; spores 8, 7-8 X 13-16 pm.
irregular, contiguous, apically subrotund, 2-4 mm +
CHEMISTRY.-cOrteX K yellowish, medulla K -,
wide, sometimes marginally dissected, becoming C-, KC-, P + red; atranorin, usnic acid, and
lobulate and crowded toward the center, with nu- physodalic acid.
merous pycnidia; lower surface black and sparsely DIsTRIBUTIoN.-Australia and Chile.
rhizinate but with a rugose bare brown zone at the HABITAT.-on branches and trunks of shrubs and
margin near the tips. Apothecia common, adnate trees in arid habitats up to 1200 m elevation.
to substipitate, 2-5 mm in diameter, the rim cre- REiMARKs.-This species was almost always iden-
nate; spores 8, 8-10 X 15-18 pm. tified as Parmelia rutidota until the chemistry
CHEMISTRY.-cortex K - , medulla K - , c - , was clarified by Kurokawa (1967). Pseudoparmelia
KC- or KC+ rose, P + orange; usnic acid, proto- rutidota contains protocetraric acid and generally
cetraric acid, and the conformata unknown. has a more expanded, thallus. While described from
DIsTRIBUTIoN.-Southeastern Brazil and Uruguay. Australia, P. ferax seems to be most common in
HABITAT.-& trees in open forest at 300-600 m Chile.
elevation.
SPECIMENS ExAh%INEo.-Australia: South Australia, Rogers
REMARKs.-This species is closely related to P.
1320, 1326 (US); Victoria, F i l s m 6597 (US). Chile: Aconcagua,
rutidota in chemistry and morphology. It produces Follrnann 11784-L (US): Nuhle, M a h u 3538 (US); Santiago,
an unidentified substance, the conformata un- M a h u 1117, 2034, 3334 (US), Santesson 7124 ( S , US); Valpa-
known, just below protocetraric acid in the hexane raiso, Imshaug 36657 (MSC), R u n d e l 7335 (US).
solvent, the same chemistry known for its presump
tive isidiate morph, the saxicolous P. papillosa. T h e Pseudoparmelia geesterani
lobes tend to be thinner and more filiform and
finely lacinate than typical P. rutidota. It occupies 11 e
FIGURE
a restricted range in Brazil and Uruguay, whereas Pseudoparmelia geesterani (Hale) Hale, 1974:190.
P. rutidota occurs sporadically in the Andean chain Parmelia geesterani Hale, 1972h:344 [type collection: Trans-
and in northern Brazil, as well as in North America vaal, Union of South Africa, Maas Geesteranus 6405 (L,
and Australia. holotype; LD, US, isotypes)].
the type collection. It is not closely related to any 42843, 44667, 44676. Chile: Magallanes, Santesson 1924 (S, US).
other Psezidoparmeliae although it might be con- Argentina: Santa Cruz, Santesson 7079 (S, US). Antarctica:
Graham Land, L a m b 2644 (FH, US); Cap Fan Beneden, Ger-
fused with isidiate-pustulate P. owariensis (4sahina)
lache (TUR, Vainio herbarium numbers 2840, 2841, syntypes
Hale or P. imperfecta (Kurokawa) Hale. of P . antarctica).
DEsCRIPTIoN.-Thallus adnate on twigs, soft and eous and has a different aspect. It appears to be best
fragile, buff mineral gray, 3-5 cm broad; lobes sub- developed in dry sea-level forests of smaller islands.
irregular, apically rotund, 1.5-2 mm wide; upper SmcnrExs ExA\cmm.-Records from the Bahamas, Grand
surface more or less regularly rugose and wrinkled, Cayman, and Haiti are listed in Hale (1971332).
the cortex easily breaking away, heavily pycnidiate;
lower surface black and moderately rhizinate except
for a narrow brown, bare zone at the tips. Apothecia Pseudoparmelia intertexta
substipitate, 2 mm in diameter; spores 8, 5-8 X FIGURE
12d
10-12 pm.
CHEMISTRY.-cOrteX K + yellow, medulla K $- Pseudoparmelia i7itertexta (Montagne and van den Bosch)
Hale, 1974:190.
yellow, C-, KC-, P + orange; atranorin, stictic Parnielia i n t e r t e x t a Montagne and van den Bosch in Mon-
acid, and constictic acid. tagne, 1896:327 [type collection: Java, Junghuhn (L, lecto-
REMARKS.-The chemical constituents and rugose type; PC, isolectotype)].
upper surface place P. inhaminensis close to P. CTO- Parrnelia ecoronata Nylander, 187354 [type collection: Pulo-
Penang, Malaya, Collingham [Cunningham in publication]
zalsiana (Bouly de Lesdain) Hale, which is sorediate,
(H, Nylander herbarium number 32999, lectotype)].
and P. sc.r.obicuZaris (Krempelhuber) Hale, which Parrnelia subrupta NJlander in Xylander and Crombie, 1883:
is nonsorediate and has a pruinose apothecial disc, 51 [type collection: Allagajah, near Malacca, Malaya,
a smaller, very rugose thallus, and unusually large hlaingay (BM, lectotype; H, isolectotype)].
conidiospores (about 20 pm long). T h e conidio- Parmelia gracilis hliiller Argoviensis, 1887:317 [type collec-
tion: Daintree River, Australia, Pentzke (G, lectotype); not
spores of P. inhaminensis are about 12pm long. It is Parrnelin gracilis (Persoon) Sprengel, 18273277 (= Usnea)].
a possible candidate as nonsorediate progenitor of Parrnelia relicina var. ecoronata (Nylander) Muller Argovi-
P. crozalsiana. ensis, 1891:378.
Parnzelia gracilenta Vainio, 1900:6 [type collection: Based on
SPECIhrEhS EXAMINED.-.hgOla: Mocamedes, L)egeliUS (De-
Parrnelia gracilis Muller Argoviensis].
gelius herbarium, US).
DEscRIPTIoN.-Thallus closely adnate, corticolous,
marguerite yellow, 3-10 cm in diameter; lobes sub-
Pseudoparmelia inornata linear-elongate, 0.5-2 mm wide; upper surface more
12c
FIGURE or less convex, faintly maculate; lower surface pale
brown to tan, densely rhizinate, the rhizines simple
Pseudoparmelia inornata (Hale) Hale, 1974: 190. to densely branched, pale. Apothecia numerous,
Parrnelia inornata Hale, 197la:32 [type collection: Grand
adnate, 0.7-2 mm in diameter; spores 8, 3-5 X 5-7
Cayman, Imshaug 24454 (MSC, holotype; US, isotype)].
Pm.
DEscRIPTIoN.-Thallus adnate on bark, pale CHEMISTRY.-cOrteX K 4- yellowish, medulla K -,
greenish mineral gray, 5-10 cm broad; lobes sub- C-, K C f rose, P f orange red; atranorin, proto-
irregular, apically rotund, 3-7 mm wide; upper cetraric acid, protolichesterinic acid, and usnic acid.
surface plane, continuous to cracked with age, usu- DISTRIBuTroN.-Andaman Islands, Thailand, Ma-
ally densely pycnidiate, white-reticulate at the lobe laysia, Philippines, Indonesia, New Guinea, and
tips; lower surface black and sparsely rhizinate ex- Australia.
cept for a narrow bare, brown zone at the margins. HABITAT.-on canopy branches of trees (diptero-
Apothecia common, substipitate, 2-4 mm in diam- carps and Quercus) in rain forest at 150-1600 xn
eter; spores 8, 7-8 X 16-18 pm. elevation.
HEMI IS TRY .-cortex K -k yellow, medulla K - , REMARKs.-This is one of two Pseudoparmeliae
C-, KC+ rose, Pf red; atranorin and proto- (the other being P. malaccensis (Nylander) Hale)
cetraric acid. that have evolved in the Southeast Asian rain for-
DISTRIBUTION.-\~eSt Indies. ests, primarily on dipterocarps. T h e only other com-
HABITAT.-oD. trees in shaded woods near sea mon parmelioid genus there is Relicina (Hale,
level. 1975b), which is also characterized by a closely
REhfARKS.-This rather broad-lobed species might adnate habit and presence of usnic acid. Pseudo-
be considered as a possible progenitor of isidiate P. parmelia intertexta is a presumptive nonisidiate
martinicana (Nylander) Hale, but it is more coriac- progenitor of P . malaccensis (Nylander) Hale (see
NUMBER 31 35
discussion under that species), although it is anom- apically subrotund, 1.5-3 mm wide; upper surface
alous in having branched rhizines. plane to rugulose, shiny, sorediate, the soralia orig-
inating from coarse pustular ridges, becoming irregu-
SPECIMENS ExAhzlNED.-Andaman Islands: KUrZ 3 (M, UPS,
W). Thailand: Chang, Schmidt XVI (TUR). Malaya: Pahang, lar to diffuse; lower surface black and moderately
Hale 30184, 30225, 30482, 30498; Selangor, Hale 30073, 30260, rhizinate. Apothecia adnate, 3-5 mm in diameter;
30261, 30264, 30299, 31188. Philippines: Mountain Province, the rim sorediate; spores 8, 5 X 10-12 pm.
Hale 25811; Negros Occidental Province, Hale 26422, 26511, CHEMISTRY.-cOrteX Kf yellow, medulla K-,
26523. Malaysia: Sabah, Hale 28206, 28813, 29065, 30363,
30364. New Guinea: Versteegh (L, US).
+ +
C , KC red, P - ; atranorin and lecanoric acid.
DIsTRIBuTIoN.-Austra~ia, New Zealand, and
Chile.
Pseudoparmelia ischnoides HABITAT.-On trees (Drachophyllum, Myrsine,
Hymenanthera, and Betula) in open woods at low
FIGURE12e
elevations.
Pseudoparmelia ischnoides (Kurokawa) Hale, 1974:190. RElhlARKs.-The lobe configuration places this
Parmelia ischnoides Kurokawa in Hale and Kurokawa, 1964: austral species near P . texana (Tuckerman) Hale,
155 [type collection: Window Stream, Kirstenbosch, Wyn-
but the soralia are more diffuse and the chemistry is
berg, Cape Province, Union of South Africa, Almborn
1698 (LD, holotype; TNS, US, isotypes)]. distinct. T h e parallel isidiate morph is probably
P. conlabrosa Hale; there seems to be n o fertile
DEscRIPTIoN.-Thallus closely adnate on rock, progenitor. T h e syntype of P. tenuirima var. labrosa
fragile, whitish ashy gray, 4-10 cm in diameter; ( T h o m s o n 2A 683 in W) is Parmotrema reticulatum
lobes sublinear-elongate, 0.5-2 mm wide; upper sur- (Taylor) Choisy.
face plane to convex, continuous, isidiate, the isidia
SPECIMENS ExAmNED.-chile: Chiloe, Santesson 2262 (s).
short, simple, darkening at the tips; lower surface Other records from Australia and New Zealand are listed in
black, sparsely rhizinate. Apothecia adnate, 1-2 mm Hale (1968:325).
in diameter, the amphithecium isidiate; spores 8,
5-6 X 7-8 pm.
Pseudoparmelia lecanoracea
CHEMISTRY.-cOrteX K + yellow, medulla K +
yellow, C-, KC-, P + pale orange; atranorin, stic- FIGURE
13a
tic acid, and constictic acid.
Pseudoparmelia lecanoracea (Muller Argoviensis) Hale, 1974:
DIsTRIBuTIoN.--union of South Africa. 190.
HABITAT.-on rocks in open areas. Parmelia lecanoracea Muller Argoviensis, 1888:529 [type col-
REMARKs.-This species has a very limited range lection: Arisdrift, Oranje River, Namaqualand, Union of
in South Africa and probably represents a typical South Africa, Schenck 543 (G, lectotype)].
Cape endemic. It bears a superficial resemblance to
DEscRIPTIoN.-Thahs closely adnate, appearing
two other small saxicolous species, P . annexa (Kuro-
areolate at the center, pruinose whitish buff, 2-3 cm
kawa) Hale (lecanoric acid present) and P. arcana
(Kurokawa) Hale (fatty acids, pale below). broad; lobes sublinear, 0.6-1.0 mm wide, black
rimmed; upper surface convex, rugose with age,
SPECIMENS EXAhfIXED.-~ee Hale and Kurokawa (1964:156) roughened; medulla pigmented reddish yellow in
for records in the Union of South Africa.
the lower half; lower surface tan or darkening, mod-
erately rhizinate, the rhizines brown. Apothecia
Pseudoparmelia labrosa rare, adnate, 1 rnm in diameter; spores 8, 7 X 8-10
FIGURE
12f CHEMISTRY.-cOrteX K + yellow, medulla K-,
Pseudoparnielia labrosa (Zahlbruckner) Hale, 1974:190. C f , KCf rose; atranorin and evernic acid; pig-
Parmelia tenuirirna var. labrosa Zahlbruckner, 1941:lo8 [type mented medulla K + purple, skyrin present.
collection: Saddle Hill, Dunedin, New Zealand, Thomson DIsTRIBuTroN.-~nion of South Africa.
V34 (W, lectotype)]. HABITAT.-On rocks.
Parrnelia labrosa (Zahlbruckner) Hale, 1968:325.
REMARKS.-ThiS species is still only known from
DESCRIPTIoN.-Tha11us adnate on bark, light buff the rather fragmentary type collection. As Muller
mineral gray, 4-8 cm broad; lobes subirregular, noted, it could be confused with a Lecanora. T h e
36 SMITHSOSIAK C O N T R I B U T I O N S TO B O T A S Y
chemistry is anomalous for the genus. It is included yellowish green, 2-8 cm in diameter; lobes short,
here in the hope that future workers will be in a sublinear, 0.5-1.5 mm wide; upper surface plane
better position to assess its exact relationship. to convex, shiny, distinctly white reticulate at the
lobe tips, tangentially cracked with age, isidiate, the
isidia simple, 0.2-0.5 mm high; lower surface pale
Pseudoparmelia leucoxantha brown, densely rhizinate, the rhizines simple to
FIGURE
13b sparsely branched, becoming dark brown. Apo-
thecia rare, adnate, 1-2 mm in diameter; spores 8,
Pseudoparmelia leucoxantha (Muller Argoviensis) Hale, 1974: 4-5 X 6-7 pm.
190. CHEMIsTRY.-cortex K + yellowish, medulla K-,
Parmelia leucoxantha Muller Argoviensis, 1881:85 [type
collection: Brazil, Sao Paulo, Puiggari 1050 (G, lectotype;
C-, KC+ rose, P f red; protocetraric acid and
W, isolectotype)]. usnic acid.
DISTRIBUTION.-Africa, India, Sri Lanka, Indo-
DEscRIPTIoN.-Thallus adnate to loosely attached nesia, Malaysia, and the Philippines.
on rock or bark, dull greenish yellow, 3-6 cm broad; HABITAT.-On trunks and canopy branches of
lobes subirregular, apically rotund, 3-5 mm wide; trees in lowland rain forest from sea level to 150 m
upper surface plane, rimose with age, sorediate elevation.
along the margins and in part on the surface, REMARKS.-while 1 tentatively consider this as
soralia irregular i n capitate or elongate masses, the the isidiate morph of P. intertexta, mostly because
soredia coarse; lower surface black and sparsely of the chemical characters and similar habitat in the
rhizinate except for a brown, bare or papillate zone lowland rain forest of Southeast Asia, the two
along the margins. Apothecia rare, sessile, u p to 2 species have diverged considerably in rhizine struc-
mm in diameter, the amphithecium sorediate; ture. T h e rhizines of P. malaccensis are simple and
spores not developed. often turn darker brown that the lower cortex; they
CHEiwsTRY.-cortex K + yellowish, medulla K -, are pale and rather richly branched in P. intertexta.
C--, KC- or KC+ rose, P + red; atranorin (trace), T h e upper cortex is strongly white-reticulate in P.
usnic acid, and protocetraric acid. malaccensis, continuous in P. intertexta.
DIsTRIBuTroN.-Mexico and Brazil.
SPECIMENS ExAhlINED.-IVOry Coast: Santesson 10397a (UPS,
HABITAT.-oII sandstone boulders, more rarely
US). India: Tamil Nadu, Hoeg (Awasthi herbarium, US).
on trees, in dry scrubby areas (chapada vegetation Sri Lanka: Fosberg 51032 (US). Philippines: Basilan, Hale
in Brazil) at 300-1 100 m elevation. 24941, 25331; Zamboanga del Norte, Hale 24727; Zamboanga
REhfARKS.-There is considerable resemblance to del Sur, Hale 24859. Malaya: Selangor, Hale 30055, 30068,
Pseudoparmelia caperata (L.) Hale in lobe config- 30262, 30266, 30284, 30292, 30295, 31187. Sarawak: Hale 29992,
uration, but the soralia are more discrete and dis- 29994, 29998, 30000. Sabah: Hale 30353, 30362, 30368. Indo-
nesia: Java, Spanjaard 6102 (L).
tinctly marginal and lateral. It may well have
evolved from nonsorediate P. rutidota (Hooker
and Taylor) Hale but differs in substratum. Parmelia martinicana
SPECIMENS EXAhiIIVED.-Mexico: Oaxaca, Hale 20643, 20648. FIGURE13d
Brazil: Maranhao, Eiten and Eiten 4497A (US); Mato Grosso, Pseudoparmelia martinicana (Nylander) Hale, 1974:190.
Malme (S); Sao Paulo, Schindler 4564b (KR, US). Parmelia martinicana Nylander, 1885:609 [type collection:
Martinique, Tardin (H, lectotype)].
+
CHEMISTRY.-cOrteX K yellowish, medulla K-, Parmelia perfissa Steiner and Zahlbruckner, 1926:519 [type
C S , KC+ rose, P + orange red; atranorin, gyro- collection: Port Elizabeth, Cape Province, Union of South
Africa., Brutznthaler PV,lectotype; WU, isolectotype)].
phoric acid, and protocetraric acid (rarely with
norlobaridone). DESCRIPTION.-Tha~~Us adnate to appressed on
DrsTRIBuT1oN.-Southeastern United States, Mex- rock, whitish mineral gray, 4-8 cm broad; lobes sub-
ico, West Indies, and Venezuela. irregular, apically rotund, crowded toward the
HABsrAT.-On tree trunks and branches i n pas- thallus center, 2-3 mm wide; upper surface plane,
tures a?d secondary forests from sea level to 1000 rimose with age; lower surface dark brown and
m elevation. blackening, moderately rhizinate. Apothecia numer-
REMARKS.-ThiS is one on the commonest foliose ous, adnate, 1-2.5 mm in diameter; spores 8, 5 X 6
lichens in scrub forest and dry savanna in the West Pm.
Indies. I t may be related to nonisidiate P. inornata CmmsTRY.-Cortex K + yellow, medulla K -,
(Hale) Hale but has a thinner, more fragile thal- C t , KC+ red, P--; atranorin and lecanoric acid.
lus. It is most closely related to P. raunhiaeri DIsTRIBuTIoN.-Uganda and Union of South
(Vainio) Hale, which is distinctly coarsely pus- Africa.
tulate-sorediate. One specimen (Allard 17325) con- HABITAT.-on rocks in open or partly shaded
tained norlobaridone in addition to protocetraric habitats from sea level to about 1200 m elevation.
acid, but further collections should be examined REMARKS.-PSeUdo~al-melia moly bdiza is espe-
before deciding whether this population represents cially common in Cape Province. T h e isidiate morph
a distinct species or not. appears to be P. annexa (Kurokawa) Hale. T h e
SPECIAIE%S ExA\rINED.-United States: Florida, Hale 36813, brilliant C f red test identifies it immediately. Pseu-
36864. Mexico: Veracruz, Hale 19743. Bahamas: illerrill (US), doparmelia spodochroa (Kurokawa and Filson)
Britton 942, 1080 (FH). Cuba: Pinar del Rio, Inishaug 25289 Hale, P. tortula (Kurokawa) Hale, and even P.
(MSC); Guantanamo, Hzoram 2701 (US); Oriente, Hioram uanderby Zii (Zahlbruckner) Hale are very similar
5477, 5706 (US). Dominican Republic: Allard 17325 (US),
externally and occur in the same localities where
W e t m o r e 3922 (MSC), 3947 (MSC, US). Puerto Rico: Britton
1691 (FH, NY). St. Croix: Britton 75 (NY, US), Boergessen P. molybdiza is found. They would be differen-
(C), Raunkiaer 547 (C), Paulsen (C). St. Martin: Le Gallo tiated by a negative C test.
478b, 571 (US). St. Barthelemy: L e Gallo 415, 497, 515, 521,
SrEciarEivs ExAMlSED.-uganda: Pian County, Sroinscow
542a, 545, 563 (US). Guadeloupe: Culberson 14536, 14544
2U 31/10A (BM, US). Union of South Africa: Natal, A l m -
(DUKE), Degelius (Degelius herbarium) Duss (C), 489 (NY),
born 8645, Hoeg ( T R H ) ; Transvaal, Maas Geesteranus (L);
Le Gallo 465, 471, 489, 574, 575, 580 (US), 2729 (MSC), 2741
Basutoland, Kofler (LD); Orange Free State, A h b o r n 5818,
(BM). Dominica: Imshaug 33159, 33282 (MSC) (other records
5831, 5834 (LD); Cape Province, Almborn 1803, 2065, 2066,
listed in Hale, 1971:18), Martinique: Culberson 14732 (DUKE),
2M7, 4837, 4948, 4980, 5690, 11115 (LD), Degelius SA-39
Degelius (Degelius herbarium), Jardin (H). St. Lucia: Imshaug
(US), H 6 e g (LD, T R H ) , M a a s Geesteranus 6706, 6707, 6730
29701, 29968, 30144 (MSC), Evans 75 (FH, NY, YU), 101
(US). St. Vincent: EIliott (TUR), Itnshaug 30369, 30692 (I>).
(MSC).Tobago: Imshaug 31565 (MSC). Trinidad: Broadway
8099 (BM). Venezuela: Magdalena, firoadway 805 (US).
Pseudoparmelia nairobiensis
FIGURE13f
Pseudoparmelia molybdiza
FIGURE13e Pseudoparmelia nnirobiensis (Steiner and Zahlbruckner) Hale,
1974: 190.
Pseudoparmelia mol) bdiza (Nylander) Hale, 1974:190. Partnelia nairobiensis (neirobiensis? Steiner and Zahlbruck-
Parrtzelia rnolybdiza Nylander in Crombie, 1876a:19 [type ner, 1926:517 [type collection: Nairobi, Kenya, Schroder
collection: T a b l e Mountain, Cape of Good Hope, Union of 287 (W, lectotype)].
South Africa, Eaton (BM, lectotype; H, Nylander herbarium Parmelia gracifescens var. angolensis Vainio in Welwitsch,
number 35234, isolectotype)]. 1901:401 [type collection: Serra da Xella, Huila, Angola,
Partnelia atricliotdes Nylander in Crombie, 187613:167 [type Welujitsch 30 pro parte ( T U R , Vainio herbarium number
collection: Cape of Good Hope, Union of South Africa, 3059, lectotype)].
Eaton (BM, lectotype; H , isolectotype)]. Parmelia angolensis (Vainio) Dodge, 1959:103.
Parwelia brachyphylla Muiller Argoviensis, 1886:256 [type Parmelia ganguelIensis Dodge, 1959: 109 [type collection:
collection: Near Lydenburg, Transvaal, Union of South Ganguelas and Ambuelas, Benguela, Angola, Gossweiler
Africa, W i [ t n s 2752 (BM, lectotype). (BM, lectotype)].
NUMBER 31
39
collection: Australia (H, Wylander herbarium number genitors?) of the sorediate morph P. caperata (L.)
35731, lectotppe; F H , isolectotype)]. Hale, the pustulate morph P. baltimorensis (Gyel-
Parmelia caperata f. rafnealis Nylander, 1861:373 [type col- nik and F6riss) Hale, and the isidiate morph P.
lection: Andes, Bolivia, Mandon (H, Nylander herbarium
number 35692, lectotype; FH, S, isolectotypes)]. papillosa (Gyelnik) Hale. None of these fit their
Parmelia jelinekii Krempelhuber, 1868:321 [type collection: respective roles perfectly but together they form a
Australia, Jelinek 27 (M,lectotype; W, isolectotype)]. coherent species group.
Parmelia ochroleuca Muller Arguviensis, 1882:306 [type col- Chemical variation centers around the presence
lection: Near Illawarra, Australia, Kirton 1 ( G , lectotype);
or absence of fatty acids, in most cases caperatic
not Parnaelia ochroleuca Taylor, 1848:24 (= Sticta)].
Parmelia splendidula Delise ex Nylander, 18853605 [type acid, and a medullary pigment. There seems to be
collection: Peru (a,Nylander herbarium number 35733, no geographic pattern here, but assuredly many
lectotype)]. more field studies and collections are needed to
Parrnelia caperatula (Kylander) Nylander, 1885:606. determine this. For the present a rather broad spe-
Parmelia subcaperatula Nylander, 1885:606 [type collection:
cies concept seems unavoidable.
Derwent River, Tasmania, Brown (H, Nylander herbarium
number 35730, lectotype; BM, isolectotype)]. SPECIMENS EXAblINED.-United States: Texas, Darrow 4863
Parmelia confertula Stirton, 1899:77 [type collection: Bris- (US), Hale 5316, 5504, Heller in Lichenes boreali-americani
bane, Australia, Bailey (BM, lectotype)]. 197 and Decades of North American Lichens 260 (US),
Hubricht B1891, B1927, Jerrny (US), Jones (US), Orchard 4
DEsCRIPTIoN.-Thahs adnate to appressed on (US), Slater 3 (US), Whitehouse 2283, 2289, 2290 (US). Mex-
bark, light greenish yellow, 3-8 cm broad; lobes sub- ico: Tamaulipas, Nakanishi 184 (US), Purcell 5564, 5601 (US).
irregular, apically rotund, contiguous, 2 4 mm Bolivia: Mandon (BM). Brazil: Pernambuco, Xavier 776,
815, 816, 826. Chile: Valparaiso, Follrnann 13013 (US). Uru-
wide; upper surface plane or becoming rugulose
guay: Lorentz 740 ( M ) ; Minas, Heiter 90669 ( H ) . Argentina:
and cracked on older lobes; medulla white but Lorentz (M). Australia: New South Wales, Degelius A-37,
sometimes with a reddish pigment near the lower A-38 (Degelius herbarium, US), Doing (L, US), D u Rietz 683,
cortex; lower surface black, shiny, sparsely rhizinate, 693 (UPS, US), Hamildon L1812 (XSiV), W a t t s L1817 (NSW);
usually with a bare dark brown naked zone at the South Australia, Rogers 1463, 1697 (US); Western Australia,
tips. Apothecia common, sessile, the rim crenate, Irvine ( G ) ; Tasmania, Pearcey (BM); Victoria, Filson 5419
(US); Australian Capital Territory, Weber in Lichenes Ex-
1-3 mm in diameter; spores 8, 7-10 X 14-20 pm. siccati 268 (US).
CHEMISTRY.-cOrteX K - or K + yellowish, me-
dulla K--, C-, KC- or KC+ rose, P f red; usnic
acid, rarely atranorin, protocetraric acid with or Pseudoparmelia salacinif era
without associated unknowns, and with or without FIGURE
15f
caperatic acid (and protolichesterinic acid?) and
+
unidentified K purple pigments. Pseudoparmelia salacinifera (Hale) Hale, 1974:191.
Parinelia salacinifera Hale in Hale and Kurokawa, 1964:157
DIsTRIBuTI0N.-United States, Mexico, South
[type collection: Sanford, Seminole County, Florida, Ru@
America, and Australia. (US, holotype; FLAS, isotppe)].
HABITAT.-on trunks and branches of trees in
semiarid regions at 100-2000 m elevation. DEsCRrPTroN.-Thallus adnate on bark, light ashy
REMARKs.-Pseudoparme~ia rutidota is a rather buff, 6-12 cm broad; lobes subirregular, apically
variable species, as one might assume from the long subrotund, 3-5 mm wide; upper surface plane to
list of synonyms. It occurs very commonly in certain rugulose, fissured with age, moderately isidiate, the
semiarid regions, especially Texas in the United isidia simple, to 0.3 mm high; lower surface brown
States and New South Wales in Australia. Outside to tan, moderately rhizinate except for a narrow
of this it is relatively rare. T h e comparable African naked zone along the margins. Apothecia rare, 2-4
populations appear to consist entirely of P . am- mm in diameter, the amphithecium isidiate; spores
plexa (Stirton) Hale, a smaller, more congested 8, 8-9 X 13-16 ,pm.
species with a black velvety lower surface. On the CHEMISTRY.-cOrteX K + yellow, medulla K f
other hand, some specimens from Mexico and South yellow turning red, C-, KC-, P + pale orange;
America are quite a bit larger than the average. atranorin and salazinic acid.
Obviously environmental modification plays a role DIsTRIBUTION.-~Outheastern United States, Mex-
in this variation. Basically P . rutidota could be, or ico, Central America, West Indies, Colombia, Vene-
closely resemble, a now extinct progenitor (or pro- zuela, Brazil, and Thailand.
46 SMITHSOSIAN C O S T R I B U T I O S S TO B O T A N Y
HABITAT.-On trees (deciduous trees, palm, con- will be more frequently collected as lichenologists
ifers) in open or secondary forest from sea level to visit coastal localities in East Africa.
1000 m elevation. SPECIMENS
ExAar!sED.-hfopcbique: Afogg 2099 (PRE, US).
REhfARKs.-The distinguishing features of this
species are the isidia and pale brown lower surface.
T h e only other comparable salazinic acid-containing Pseudoparmelia schistacea, new combination
species is saxicolous P. scotophylla Kurokawa from Pa, iirelia scliistacea Kurokawa and Filson, 1975:44 [type col-
Australia. It has a smaller thallus and small spores. lection: 65.5 km west of Kingoonya, South Australia, Filson
Pseudoparmelia cinerascens (Lynge) Hale has a 11921 (hIEL, holotjpe) (not seen)].
black lower surface. T h e only other species that
could be confused with it because of the similar DESCRIPTIoN.-ThallUS closely adnate, pale oliva-
habitat, range, thallus color, and lobe configuration ceous gray, 2-4 cm broad; lobes sublinear-elongate,
is P. amazonica (Nylander) Hale, which has a crowded at the center of the thallus, 0.5-1.5 mm
black lower surface and contains protocetraric acid wide; upper surface plane to convex, shiny, be-
coming tangentially rimose, pustulate; medulla
(K-h white; lower surface pale brown, sparsely rhizinate.
S[,Ecihims EXAMiNED.--Cnited States: Georgia, Hale 16843; Apothecia not seen.
Florida, H a l e 7994, 16714, 17045, 17083, 17735, 21690, 21967,
Moore 4406 (DUKE, US). R a p p (FLAS, US), Standiey 13084
CmMIsrRY.-Cortex K +
yellow, medulla K -,
(US). See Maore (1968:225) for further records from Florida. C-, KC-, P-; atranorin, a trace of usnic acid,
Merico: Chiapas, Hale 20607. Honduras: Comayagua, Standley caperatic acid, and an unidentified fatty acid.
6522 (F, US); Cortes, Morton 5896 (US). Cuba: Pinar del Rio, DISTRIBLIT~~N.-Australia.
Ztnshaug 25215 (MSC, US). Jamaica: Plitt (US). Colombia: HABITAT.-on rocks in open areas.
Santander, A'ee and M o r i 3736 (US). Venezuela: Maracay,
REMARKS.-The authors of this species compare
Nasli 1946 (US). Brazil: M a r a n h a o , Eiten 4198 (US); Mato
Grosso, Afaltiie (UPS). Thailand: Kurokawa 1931 (TNS, US). i t with P. arcana (Kurokawa) Hale, both having
closely adnate, almost subcrustose thalli. They have
different morphologies, however, P. arcana being
Pseudoparmelia schelpei
typically isidiate. A trace of usnic acid is alleged to
FIGLRE16a occur in P. schistacea. T h e species is illustrated in
Kurokawa and Filson (1975, pl. 4: fig. 1).
Pseudoparttieha schelpei (Hale) Hale, 1974:191.
Pa? inelia sclfelpei Hale, 1972b:344 [ty pe collection: Maxixe,
Sul do Sate, hlocambique, Sclielpe 4460 (BOL, holotype; Pseudoparmelia scotophylla, new combination
LD, US, isotypes)].
FIGURE166
DESCRIPTIoN.-ThalluS closely adnate on bark,
whitish mineral gray, 2-4 cm broad; lobes sublinear, Partrielin scotophl lla Kurokawa in Kurokawa a n d Filson,
crowded, 1.5-2.0 mm wide; upper surface plane, 1955 45 [type collection. Ardglen Gap, Liberpool Range,
S e w South TVales, Australia, Kuiokauw 5174 (TNS, holo-
dull, rugulose with age; lower surface black, t\pe; MEL, isotjpe) (not seen)].
sparsely rhizinate. Apothecia numerous, adnate, 1-2
mm in diameter; spores 8, 4 X 8-10 pm. DESCRIPTIoN.-Thallus closely adnate, whitish to
CHEMISTRY.-cOrteX K+ yellow, medulla K - , dark mineral gray, 4-12 cm broad; lobes sublinear,
C-, K- or KC+ rose, P + orange; atranorin and congested, apically subrotund, 1-2 mm wide; upper
protocetraric acid. surface plane, shiny, becoming densely isidiate, the
DIsTRrBuTroN.-h~ocambique. isidia cylindrical, simple, the tips blackened; lower
HABITAT.-on coconut palms near sea level. surface dark brown or blackening, sparsely to mod-
REMARKS.--NOother species in Pseudoparmelia erately rhizinate, the rhizines brown or black, sim-
has protocetraric acid and such narrow lobes. Pseu- ple. Apothecia (from type description) substipitate,
doparmelia caribaea (Hale) Hale, a saxicolous 6 m m in diameter, the amphithecium isidiate;
species in the West Indies, is much larger. T h e spores 8, 5 X 7-8 pm.
sorediate morph of P. schelpei is presumed to be CHEMISTRY.-cOrteX Kf yellow, medulla K +
P. epileuca (Hale) Hale, which also occurs in Mo- yellow turning red, C-, KC-, P + orange; atra-
cambique as well as in Kenya. I suspect both species norin and salazinic acid.
NUMBER 31
47
Louisiana, Langlois 47 (US); Texas, Jenny (US); Florida, lobe surface is smooth and shiny except for Degelius
Calkins 2 (US), Culberson 10893 (DUKE, US), Hale 16728, SA-57, which has a roughened, almost coarsely
16889, 17652, 17738, 21623, 34134, 36829, 36887, hash 2035
(US), RaPP 19, 2086 ( U S ) . R a p p in Cryptogarnae Vindobo-
pruinose surface, a trait seen in specimens of other
nenses 3654 (US), R a p p in Lichenes Rariores Exsiccati 379 genera that grow in exposed desert regions. Further
(BM, UPS, US), Standley 73421 (US) (for further records from collecting in Africa and Australia will be needed to
Florida see Moore 1968:224). Mexico: Jalisco, W i r t h (US); decide whether the limits of the species as described
Chiapas, Hale 20030, 20174. Guatemala: Baja Verapaz, Hale here are too broad.
45998, Xellerrnan 8045 (US). Panama: Cocle, Hale 43571;
Panama, Hale 38546. Costa Rica: T o n d u z (US). Bahamas: SPECIMENS ExA~~iv~D.-Australia:Australian Capital Terri-
Brace 6792 (FH, S Y ) . Cuba: Wright 76 (BM, FH, G, XY, tory, Weber L-47220. L-47282 (COLO, US). Union of South
UPS, US); Pinar del Rio, Imshaug 25349, 25376 (MSC). Haiti: Africa: Cape Province, Alniborn 4900 (LD, US), Degelius
Nord, Leonard 8023 (S, US), 9002 (NY). Dominica: Hale SA-57 (Degelius hcrbarium, US).
35636, 35775, 35779. Venezuela: Distrito Federal, Dennis 1548
(BM); Guarico, Goodland 2 (US), Nilson 1500 (UPS). Peru:
San Martin, Allard 2294a, 22295a (US). French Guiana: Pseudoparmelia subambigua, new species
Degelius (Degelius herbarium). Brazil: Spruce 130 (BM);
Maranhao, Eiten 3887 (US); Goias, Iruin 32073 (NY, US); FIGURE
17b
Mato Grosso, Malrne in Lichenes Awtroamericani 96 (BM, DESCRIPTIoN.-Thalhs arcte adnatus, mollis,
LD, S, UC, US), 2642 (UC, UPS, US), Rainos 6545 (BM); SPO
Paulo, Schindler 4586 (US). Cameroon: Zenker 4053 (BR).
viridi-flavicans, 5-10 cm latus, lobis subirregulari-
Zaire: Hoieg (TRH), Louis 6765, 7151, 8482 (BR, US). Guinea: bus, brevibus, apice subrotundatis, congestis, 1.O-
Santessoti 10574 (UPS, US). Angola: Gossuqeiler 8013a (BM). 3.0 mm latis; superne planus, centrum versus rugo-
Tanzania: Hoeg (TRH). Madagascar: des Abbayes in Lichenes sus, dense sorediatus, soraliis orbicularibus, con-
Madagascarienses 5 (US). fluentibus; cortex superior 8-10 pm crassus, epicor-
tex perforatus, stratum gonidiale 20 pm crassum,
Pseudoparmelia spodochroa, new combination medulla alba, 110-120 pm crassa, cortex inferior
7-10 pm crassus; subtus niger, sparse rhizinosus,
FICCREl7a
rhizinis simplicibus, nigris. Apothecia ignota.
Parrrzelia spodochroa Kurokawa and Filson, 1975:46 [type CHEMISTRY.-cOrteX K - , medulla K - , c -l-,
collection: Warren Gorge, Flinders Range, South Australia, KCf red, P-; usnic acid and lecanoric acid.
K . Filsorz 11976 (MEL, holotype; T N S , isotype) (not seen)].
HoLoTYPE.-chile: Antofagasta, Paposo Que-
DESCRIPTION.-Tha~~usadnate on rock, whitish to brada Guanillo, elevation 880 m, M . Mahu 3405,
dark mineral gray, 3-6 cm broad; lobes sublinear, 12 September 1972 (US; Mahu herbarium, isotype).
apically subrotund, contiguous, becoming lobulate DIsmmuTIoN.-Chile.
with age, 1.5-2.5 mm wide; upper surface plane, HABITAT.-on shrubs and fence posts in open
transversely rimose with age; lower surface brown areas from sea level to 900 m elevation.
or blackening, moderately rhizinate, the rhizines REh.fARKs.-This lichen could easily be misiden-
brown or black. Apothecia (from Degelius SA-57) tified as Parmeliopsis ambigua (Acharius) Nyland-
adnate, 2-3 mm in diameter; spores 8, 6 X 8-11 er. T h e lower surface is black, however, and the
chemistry distinctive. Larger specimens may also
P.
CHEMISTRY.-cOrteX Kf yellow, medulla K + resemble Pseudoparmelia soredians (Nylander)
yellow turning red, C-, KC-, P + orange; atra- Hale, which contains salazinic acid and which may
norin, salazinic acid, and usually norstictic acid. well be the most closely related species. I t is known
DIsTRIBUTION.-AUStralia and Union of South only from Chile.
Africa. SPEClhlENS EXA?mNED.-chile: Coquimbo, Runde2 7230 (Us),
HABITAT.-on more or less exposed rocks in dry Santesson 2519 (S, US); Santiago, R u n d e l 7323 (US); Valpara-
iso, Santesson 2808 (S, US).
woodlands.
REMARKS.-This species is represented by only
five collections, which diverge rather widely in sev- Pseudoparmelia subamplexa, new species
eral characters. T h e color of the lower surface, for
17c
FIGURE
example, varies from almost entirely black to pale
brown. Chemistry is uniform except for Almborn DEsCRIPTroN.-Thallus ut in Pseudoparmelia am-
4900 and the holotype, which lack norstictic. T h e plexa (Stirton) Hale sed superficie sorediatus, soraliis
NUMBER 31
51
Parmelia mangenotii des Abbayes, 1951:969 [type collection: 20278. Honduras: Morazan, Standley 4105, 11623 (F). Costa
Mankono, Cercle of Seguela, Ivory Coast, des Abbayes Rica: San Jose, Q,uiros 1246, 1474 (US). Panama: Chiriqui,
(REN, lectotype; US, isolectotype)]. Hale 38914, Scholander (US). Haiti: Ouest, Imshaug 22537
Parnielia pseudorutidota Asahina, 1952:17 [type collection: (MSC), Wetmore 2670 (MSC, US). Venezuela: Merida, Hale
Nagachi, Shinshu, Japan, Takahashi (TNS, lectotype)]. 42121, 42920. Peru: Abancay, Iltis 2322 (WIS). Brazil: Minas
Parmelia tQnQkQeAsahina, 1954:371 [ t y p e collection: KUZU- Gerais, Eiten 6864, 6870 (US), Mosen 2309 (S, US): SaO Paulo,
Mura, Buzen, Prov. Yamato, Japan, Tanaka (TNS, lecto- Eiten 2978, 8060 (US), M i l n e 32 (BM), Osorio 4919 (MVM);
t,pe)l. Santa Catarina, Reitz and Klein 15114 (US); Rio Grande do
Parmelia QlbQnienSlSDodge, 1959:121 [type collection: forests Sul, Lima 90 (US). Uruguay: Canelones, Zorron 1929 (US);
of Albany, Cape of Good Hope, Union of South Africa, Montevideo, Osorio 1849, 6824 (MVM). Chile: Antofagasta,
Zeyher 3 (FH-Tayl, holotype)]. Rundel 7205 (US). Uganda: Busiro County, Swinscow 2U
24/4 (BM, US). Angola: Bie, Degelius (Degelius herbarium).
DEscRrPTroN.-Thallus closely adnate on trees Kenya: Rift Valley Province, MQQS Geesteranus 4551 (L).
or rocks, ashy white, 6-12 cm broad; lobes sublinear Rhodesia: Hoeg (TRH). Tanzania: Arusha Prov., Santesson
to subirregular, apically rotund, 3-5 mm wide; up- 21338 (UPS); Kilimanjaro Prov., Santesson 20948 (UPS);
Union of South Africa: Natal, Hoeg (TRH); Transvaal,
per surface plane to rugulose, usually deeply rimose,
Alrnborn 6253 (LD); Cape Province, Almborn 10664 (LD).
sorediate, the soralia laminal, punctiform to capi- Madagascar: des Abbayes in Lichenes Madagascarienses et
tate, in part initially pustulate with formation of Borbonici Selecti E X S ~ C C 11Q(LD,
~ ~ US). India: Tamil Nadu.
soredia; lower surface black and moderately rhiz- Foreau 4092 (Awasthi herbarium), Hale 40167, 43708. Thai-
inate except for a narrow naked brown zone along land: Kurokawa 1948 (TNS). Japan: Province Ohmi, Hale
29473. Indonesia: Java, Groenhart 1711 (L), Kurokawa in
the margins. Apothecia rare, 2-5 mm in diameter;
Lichenes Rariores et Critici E X S ~ C 39 ~ ~ US); Sumatra,
C Q(TNS,
spores 8,6-7 X 9-11 pm. Groenhart 957 (L). Australia: New South Wales, Flockton
CHEMISTRY.-cOrteX Kf yellow, medulla K-, 724B (US).
C - - , KCf pale violet or KC-, P--; atranorin,
divaricatic acid, and associated unknowns.
DIsTRrsuTIoN.-Pantemperate outside of Europe Pseudoparrnelia tortula
and pantropical at higher elevations. FIGURE
18a
HABITAT.-On trees ( ACaCia, Eucalyptus, Junip-
erus, Pinus, Quercus) and more rarely o n rocks in Pseudoparrnelia tortula (Kurokawa) Hale, 1974:191.
Parmelia tortula Kurokawa in Hale and Kurokawa, 1964:157
open or secondary forest and in parks and gardens [type collection: Namaqualand, Cape Province, Union of
at 50-2400 m elevation. South Africa, Almborn 4805 (LD, holotype; TNS, US, iso-
REMARKS.-This is one of the most widespread Y pes)l.
species in the genus and while not usually occur-
ring in as great abundance, for example, as P. cup- DESCRIPTION.-Thallus closely adnate on rock,
eruta (L.) Hale, it is well represented, if not whitish mineral gray, 5-10 cm in diameter; lobes
frequently misidentified, in most large herbaria. subirregular to sublinear, apically subrotund,
T h e range of morphological variation is small and crowded toward the center, 1.5-4 mm wide, often
the chemistry uniform and distinctive. It is difficult twisted and contorted when free from the substra-
to understand why so many lichenologists failed to tum; upper surface plane to rugulose or undulate,
recognize it. T h e nonsorediate progenitor may be continuous, sometimes faintly pruinose; lower sur-
represented by the African P. nairobiensis (Steiner face pale brown, sparsely rhizinate, the rhizines
and Zahlbruckner) Hale and the companion isid- brown. Apothecia adnate to substipitate, 1-5 mm
iate morph by P. concrescens (Vainio) Hale. in diameter; spores 5-6 X 7-9 ,ym.
CHEMISTRY.-cOrteX K f yellow, medulla K--,
REPRESENTATIVE SPECIMENSEXAhlINED.-united States: Wis-
consin, Thomson 10921 (US, WIS); Tennessee, Hale 37032;
+
C -, KC - or KC faint rose, P - ; atranorin, nor-
West Virginia, Hale 10308; Illinois, Skorepa 934 (us); Vir- lobaridone, and neoloxodic acid.
ginia, Hale 12814 (US); South Carolina, Culberson 7515 DISTRIBUTION.-uniOn of South Africa.
(DUKE); Alabama, Hale 34057; Georgia, Hale in Lichenes HABITAT.-on rocks in open treeless or sparsely
Selecti Exuccati 270 (US); Florida, Hale 36897; Arkansas, vegetated areas u p to 1000 m elevation.
Hale 5567. Mexico: Chihuahua, Matthews 43794 (US); Hi-
dalgo, Chase 7429 (F, US), Weber et d . 33690 (COLO);
REMARKs.-This rather undistinguished lichen is
Michoacaan, Hale 20849; Oaxaca, Cain 27578 ( T R T , US), still known only from South Africa, where it seems
Hale 20621, 20630; Veracruz, Hale 19407; Chiapas, Hale to be quite common. T h e presumptive isidiate
54 SMITHSONIAN CONTRIBUTIONS T O BOTANY
morph, P. subtortula (Hale) Hale, occurs farther pm crassa, cortex inferior paraplectenchymatus, 8-
north in Kenya and Uganda. 10 pm crassus; subtus pallide brunneolo-albus,
sparse rhizinosus, rhizinis simplicibus, pallidis. Apo-
SPECIMENS EXAMINED.-&e Hale and Kurokawa (1964:158)
for records from the Union of South Africa.
thecia ignota.
CHEMISTRY.-cOrteX Kf yellow, medulla K-,
C-, KC- or KC+ rose, P + red; atranorin and
Pseudoparmelia vanderbylii protocetraric acid.
HoLOTYPE.-Venezuela: Tachira, Pic0 Banderas,
FIGURE
18b
Pdramo de Tama elevation 3200 m, M . E . Hale
Pseudoparmelia vanderbylii (Zahlbruckner) Hale, 1974:191. 45526a, 27 March 1975 (US).
Parmelia vanderbylii Zahlbruckner, 1932a:252 [type collec- REMARKS.-ThiS inconspicuous species is easily
tion: Union of South Africa, Van Rhynsdorp, Cape Prov- overlooked in the high paramo areas where it ap-
ince, P . A . van der Byl (W, lectotype)]. pears to be confined. This is the highest elevation
DEscRIPTIoN.-Thallus closely adnate on rocks, at which the genus is found. There seem to be no
brownish or dark mineral gray, 3-6 cm broad; lobes close relatives. It would more likely be confused
subirregular, apically subrotund, contiguous, 1-2 with Parmeliopsis, which is characterized by the
mm wide; upper surface plane, shiny, rimose with presence of thamnolic acid.
age; lower surface pale brown, sparsely rhizinate, SPECIMENS EXAMINED.-VeneZUeh: Taichira, Hale 45499a,
the rhizines pale brown. Apothecia common, ses- 45523, 45528a.
sile, 1-2 mm in diameter; spores 8, 6 X 8-10 pm.
CHEMISTRY.-cortex Kf yellow, medulla K-
or Kf very faint orange, C-, KC-, P-; atra- Pseudoparmelia violacea
norin and two or more unidentified substances.
DrsTRIBuTroN.-~nion of South Africa. FIGURE
18d
HABITAT.-oII exposed rocks in open areas.
Pseudoparmelia violacea (Kurokawa) Hale, 1974: 191.
REMARKS.-This species falls near P. molybdiza Parmelia violacea Kurokawa in Hale and Kurokawa, 1964:
(Nylander) Hale in general aspect and habitat but 158 [type collection: Blinkwater Ravine, Table Mountain,
differs in chemistry. Two specimens (the lectotype Cape Province, Union of South Africa, Almborn 1771 (LD,
and Almborn 4636) have identical chemistry (two hobtype)].
spots in both the hexane and benzene solvent sys-
tems) and the third (Almborn 51 10) has distinctly DEscRIPTIoN.-Thallus closely adnate on rock,
different but still unidentified higher spots. All greenish mineral gray, 3-6 cm in diameter; lobes
three share the same two lowermost faint spots. sublinear, 1-3 mm wide; upper surface plane to
None matched any of the usual KC.- depsidones distinctly rugulose, continuous; medulla vinaceous
and depsides with which they were co-chromato- purple; lower surface pale brown, moderately rhiz-
graphed. inate, the rhizines pale. Apothecia adnate, 1-1.5
mm in diameter; spores not developed.
S P E C l h t E N S EXAhllNED.-uniOn of South Africa: Cape PrOV-
ince, Alvrborn 4636, 5110 (LD, US).
+
CHEMISTRY.-cOrteX K yellowish, medulla KS-
purple, P - ; unidentified anthraquinones.
DISTRIBUTION.-union of South Africa.
Pseudoparmelia venezolana, new species HABITAT.-on rocks in open forest.
REMARKS.-This remarkable species has been re-
FIGURE
18c collected once since the original description. It is
DEsCRIPTION.-Thallus adnatus, saxicola, cinereo- another typical saxicolous African endemic verging
albus, 3-7 cm latus, lobis sublinearibus, congestis, close to Xanthoparmelia. The pigments are, in fact,
0.6-1 .O mm latis; superne planus, nitidus, dense very close to those of X . endomiltoides (Nylander)
isidiatus, isidiis cylindricis, simplicibus vel ramosis, Hale, one being identical. No lichen substances are
0.2-0.4 mm altis; cortex superior 15-18 pm crassus, present in the cortex.
epicorticatus, epicortice distincte perforato, stra- SPECIMENS EXAMINED.-union of South Africa: Cape Prov-
tum gonidiale ca 10 pm crassum, medulla alba, 100 ince, Degelius SA-70 (Degelius herbarium, US).
56 SMITHSOXIAN CONTRIBUTIONS T O BOTANY
ever, Sprengel mentioned affinity with Parmelia species in synonymy under Cetrelia olivetorum
perforata and P. perlata, both large Parmotrema (Nylander) W. Culberson and C. Culberson.
species. Pseudoparmelia euplecta (Stirton) Hale, 1974:190.
Parmelia caperata var. coerulea Bouly de Lesdain, I have tentatively placed this species as a synonym
1954:222 [type collection: Rocamadour, France, of Pseudoparmelia caperata in the Taxonomic
Duval]. Treatment.
The type specimen is probably in PC but I was Pseudoparmelia leucopis (Krempelhuber) Hale,
not able to locate it there. 1974:190.
Parmelia protorevoluta Gyelnik, 1931b3288.
Parmelia leucopis Krempelhuber, 1878:461 [type collection:
Parinelio revoluta f. nuda Muller Argoviensis, 1891:378 [type Lorentz and Hieronytnus, Argentina (M. lectotype)].
collection: Santarem, Brazil, Spruce 135 (G, lectotype; BM,
isolectotype)]. After reexamining the type collection, I found
The fragmentary type collections contain divari- some cilia in the lobe axils. These would exclude
catic acid. This is almost certainly a Pseudo- the species from Pseudoparmelia, and I hesitate
parmelia, perhaps P. nairobiensis (Steiner and to reassign it to another genus until better mate-
Zahlbruckner) Hale, a presumed African en- rial is available.
demic. Pseudoparmelia meiosperma (Hue) Hale, 1974:190.
Parmelia rutidota var. vestita Zahlbruckner, 1941: Parmelia internexa f. rneiosfierina Hue, 1899:185 [type col-
107. lection: Mafate, Reunion, Rodriguez (PC, lectotype)].
This variety is based on two collections, one
T h o m s o n ZA217 from Southland, New Zealand, The type-specimen has rather broad lobes with
which is Parmelia rudecta Acharius, and the dense isidia. The rhizines are dense and more or
other Cranwell ZA242 from Coromandel Penin- less branched. The chemical constituents include
sula, New Zealand, which can be identified as atranorin, evernic acid, and traces of lecanoric
Parmotrema crinitum (Acharius) Choisy. Both acid, a combination that is known in several spe-
specimens are preserved in W. cies of Hypotrachyna (Hale, 1975a) but in no
Parmelia soredians f. farinosa (Vainio) Gyelnik, Pseudoparmeliae. It does not fit well in Pseudo-
1938a:27. parmelia and until additional material is avail-
This is based on Parmelia farinosa Vainio (1890: able it is impossible to settle its generic position.
62) (Lichenes Brasilienses Exsiccati 551 in Pseudoparmelia pseudofallax Gyelnik, 1933:6.
TUR). It is a species of Xanthoparmelia (Vainio) Culberson and Culberson (1968:459) consider
Hale. this to be a species of Cetrelia but not having
Parmelia soredians f. lobulata Gyelnik, 1934:306 examined the type collection they could not de-
[type collection: La Calera Sud, Argentina, Hos- cide which one.
seus 22 (BP, holotype)]. Pseudoparmelia pseudofallax var. cretaceoides Gyel-
This is a species of Xunthoparmelia (Vainio) nik, 1933:7.
Hale. This taxon also belongs in the Cetrelia cetrari-
Parmelia soredians f. muscicola Gyelnik, 1934:306 oides complex.
[type collection: Capilla del Monte, Argentina, Pseudoparmelia pseudosoTediosa (Gyelnik) Hale,
Hosseus 23 (BP, holotype)]. 1974:191.
This is also a Xanthoparmelia. This has been reduced to synonymy under Pseu-
Pseudoparmelia aradensis Gyelnik, 1933:6. doparmelia caperata in the Taxonomic Treat-
Culberson and Culberson (1969: 5 15) place this ment above.
Literature Cited
58
NUMBER 91 59
61
62 S M I T H S O N I A N C O N T R I B U T I O N S T O BOTAXY