Floristic diversity and plant composition of the arid and Saharan zones of southern
Tunisia
Adel Dhief 1, 2, *, Samira Aschi-Smiti 2 and Mohamed Neffati 1
1 Institute
of Arid Regions, Laboratory of Pastoral Ecology, 4119, Medenine, Tunisia.
of Biology, Faculty of Sciences of Tunis, 1060, Tunis, Tunisia.
2 Department
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
Publication history: Received on 17 January 2022; revised on 10 March 2022; accepted on 12 March 2022
Article DOI: https://doi.org/10.30574/gscbps.2022.18.3.0081
Abstract
Spontaneous plants in arid and desert areas of Tunisia are now experiencing a resurgence of interest not only because
of the possibilities of their use for multiple economic and ecological purposes, but also because of their great capacity
for potential climate change adaptation.
Often considered underused and neglected species, plants in arid and desert areas are of considerable importance.
The purpose of this work is to provide knowledge relating to flora and Tunisian vegetation in arid zones. They are
structured around various aspects relating to the characterization of this natural and biological wealth and its impact
on the quality of the environment. In this work, we studied the flora of the different regions visited (Tataouine,
Medenine, Tozeur, Gabes and Kebeli) in southern Tunisia and we surveyed the botanical composition and species
diversity in the governorate of Tataouine region during the spring season of 2018. The flora contained about 279 species
belonging to 58 families, with 54% annuals and 46% perennials.
Keywords: South of Tunisia; Flora; Diversity; Species richness; Drylands
1. Introduction
Located in North Africa, Tunisia is situated between longitudes 7° and 12°E and the latitudes 32° and 38°N. It is with
the junction of the Western and Eastern Mediterranean, and covers a surface of 164 000 km 2, which is the three quarters
of arid and desert regions including in particular the steppe zone in which the northern limit coincides appreciably with
the isohyet of 350 mm [1-2].
Climate change and human activity represent a big threat to biodiversity [3-4-5]. In fact, the rangelands have been
subjected to intensive anthropogenic and climatic disturbances, such as overgrazing and drought over a long period of
time, and their overall condition is deteriorating [4–5]. The continuous damage to biodiversity increases the rate of
species extinctions, which undermines our capacity to combat desertification, reduce poverty, increase food security,
and exclude invasive species. The ongoing ecosystems degradation and increasing photogenetic erosion justify plans
for restoration of arid areas. Loss of biodiversity is a major consideration in the phenomenon of desertification. For
restoration activities to be successful, knowledge of local plant species is required because of the significant role their
adaptation plays in the ecological context of restoration.
The arid regions are among the most important ecosystems and provide a great variety of services and homes to
pastoral and agro-pastoral communities. In particular, they cover diverse habitats and ecological communities. They
*
Corresponding author: Adel Dhief
Institute des Régions Arides, Laboratoire d’Ecologie Pastorale, 4119, Medenine, Tunisia.
Copyright © 2022 Author(s) retain the copyright of this article. This article is published under the terms of the Creative Commons Attribution Liscense 4.0.
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
are also economically important given the tremendous richness of edible plant, forage, medicinal, and economic species
[3-6].
The effects of any disturbance on the plant biodiversity of Arid areas are more apparent and deeper than in other
ecosystems. Several studies have shown the negative effects of biotics and abiotics factors (grazing, drought and other
human activities) on biodiversity of dryland plant species [7–8]. In the face of the degradation of natural resources and
the progress of desertification, maintenance of biodiversity through active management has recently become an
important challenge for biodiversity conservation [9]. Restoration efforts for natural diversity are important and result
in high species diversity [9–11]. Some efforts have been made to restore the functions of drylands. Floristic wealth is
considered particularly valuable and a prime target for establishing conservation priorities [12-14]. The economic,
medicinal and ecological value of desert plants requires knowledge of their botanical composition and their richness in
spontaneous species. During the period between 2008 and 2011 the flora of the arid and desert areas of southern
Tunisia was assessed (Tataouine, Medenine, Tozeur, Gabes and Kebeli) and the botanical composition of Tataouine
region was studied during the spring of 2017-2018, during which the area received an average rainfall (100 mm) and
135 species was recorded. [10].
Under these conditions, arid and desert rangelands show a great resilience illustrated through a very high plant
diversity. These rare favorable conditions offer a golden opportunity to record the greatest plant diversity in arid and
desert zones and identify key species that can survive in this ecosystem. Specifically, the objectives of our study are to
examine the diversity in the flora of the arid and desert areas of southern Tunisia (Tataouine, Medenine, Tozeur, Gabes
and Kebeli) and the botanical composition, including plant family, life form, habitat class, palatability, and medicinal and
aromatic plants, and to determine the relevance of plant diversity to arid and desert. It is important to understand the
significance of these rangelands in terms of providing several ecosystem services of vital importance for the local
communities. Our findings could contribute towards developing holistic and sustainable rangelands management
practices and finding innovative solutions to protect key natural habitats in southern Tunisia and similar arid
environments.
2. Material and methods
2.1. Study Area
Figure 1 Map of the study sites of the flora of the arid and desert areas of southern Tunisia (Tataouine, Medenine,
Tozeur, Gabes and Kebeli).
The study of the flora of the arid and Saharan zones of Tunisia was carried out directly by several field visits during the
period between 2008-2011 (Figure 1). All species were photographed using a digital camera, showing structure, leaf,
stem, flower, and fruit, if existing. All recorded plants were then identified with the help of available Tunisian flora of
Pottier-Alapetite [14-15] and by collaboration with botanists. The coordinates of the study sites are determined by a
GPS device (Table 1). The five sites of the region of Tataouine (Bir zar, ElBorma, Tiert, Oued Jnein, El Ouera) were chosen
to determine the floristic composition during the year 2008 which was very rainy. The total annual average rainfall in
251
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
the area is below 100 mm, with cold, dry, and windy winters and hot and arid summers. Sand dunes and sandy,
limestone, and gypsum soils are the most common soils in the desert area.
Table 1 Geographical distribution of study sites in southern Tunisia
Sites
Altitude (m)
regions
Coordinates GPS
Jbil
169
kebeli
Bir zar
334
Tataouine
33°141’020’’N/09°250’508’’E
ElBorma
242
Tataouine
Tiert
392
Tataouine
ElFjé
15
Medenine
Oued Jnein
280
Tataouine
Oued Dhabaa
249
kebeli
Ksar Ghilane
240
kebeli
Oued Zridib
369
Medenine
El Ouera
188
Tataouine
Djerba
3
Medenine
Nefta
52
Tozeur
Matmata
380
Gabes
31°293’535’’N/10°004’597’’E
32°033’006’’N/09°072’698’’E
30°464’235’’N/10°111’545’’E
33°295’905’’N/10°382’999’’E
31°482’265’’N/10°161’592’’E
36°776’793’’N/03°253’147’’E
32°593’606’’N/09°390’184’’E
33°151’601’’N/09°584’911’’E
32°562’928’’N/10°274’946’’E
33°807'600’’N/ 10°845'200''E
33°550'100’’N/08°080’00’’E
33°320'400’’N/09°580'170’’E
2.2. Data Collection
As a consequence of the favorable rainfall conditions recorded in southern Tunisia during 2008-2009 (Figure 2), vast
rangeland areas were covered by hundreds of bloomed plant species. The present inventory represents the highest
species richness recorded in the regions of (Tataouine, Medenine, Tozeur, Gabes and Kebeli) and in the five sites of
Tataouine. The inventory was conducted through frequent field visits made to various rangeland sites from March 2008
to April 2008 to identify different plant species (Figure 3 and table 2).
Since the areas is huge, we had to rely on expert knowledge, including herders who practice transhumance, as well as
elderly pastoralists, to guide us to the exact locations where certain species were resurfacing during such an exceptional
favorable year. All recorded plants were then identified with the help of available Tunisian flora of Pottier-Alapetite [1415]. The nomenclature for inventoried species was updated using the synonymic index of the flora of North Africa by
[16] and POWO (Plants of the World Online) [17] and by collaboration with botanists. Once plants were identified,
family, life form, habitat and class of each species were determined.
Figure 2 Variation of monthly precipitation (mm), the average monthly temperature (° C), humidity of the monthly
average air (%) and the average monthly wind speed (Km / h) during the season of 2008 in Tataouine, southern
Tunisia [18]
252
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
253
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
254
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
Figure 3 The Flora identified during the visits to the study sites of the southern Tunisia.
255
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
Table 2 The list of species identified during visits to study sites in southern Tunisia
Halophilic vegetation
Aeluropus littoralis
Anacyclus monanthos subsp. cyrtolepidioides
Artemisia herba-alba
Arthrocnemum macrostachyum [= indicum]
Atriplex glauca subsp. mauritanica
Atriplex halimus (planté)
Atriplex lindleyi subsp. inflata
Atriplex mollis
Bromus madritensis
Casuarina cf. equisetifolia
Diplotaxis simplex
Erodium glaucophyllum,
Filago mareotica
Frankenia thymifolia
Halocnemum strobilaceum
Hyparrhenia hirta
Plantago coronopifolium
Launaea resedifolia
Limoniastrum monopetalum
Limonium pruinosum
Lycium shawii [= L. Arabicum]
Lygeum spartum
Medicago minima
Mesembryanthemum cristallinum
Nitraria retusa
Ononis angustissima subsp. filifolia
Peganum harmala
Picris coronopifolia
Plantago albicans
Polygonum equisetiforme
Reichardia tingitana
Retama raetam
Rostraria salzmannii [= Koeleria salzmannii]
Salsola tetrandra
Sueda vermiculata [= mollis]
256
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
Trigonella maritima
Zygophyllum album [= Tetraena alba]
Aeluropus littoralis
Arthrocnemum macrostachyum [= glaucum]
Juncus acutus
Limoniastrum monopetalum
Limonium tunetanum
Lycium shawii
Reaumuria vermiculata
Salsola tetrandra
Tamarix africana
Zygophyllum album
Gypsophyl steppe with Erodium arborescens
Anabasis oropediorum
Anarrhinum brevifolium
Argyrolobium uniflorum
Asparagus albus
Asparagus stipularis [= horridus]
Asphodelus tenuifolius
Asteriscus hierochunticus
(= Odontospermum pygmaeum)
Atractylis cancellata
Atractylis serratuloides
Coris monspeliensis
Deverra chlorantha [= Pituranthos chloranthus]
Didesmus bipinnatus
Diplotaxis harra
Erodium arborescens
Fagonia cretica
Fagonia glutinosa
Globularia alypum
Gymnocarpos decander
Hammada scoparium
Hedysarum spinosissimum
Helianthemum crassifolium
Helianthemum intricatum
Helianthemum lippii
Helianthemum sessiliflorum
257
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
Herniaria fontanesii
Kickxia aegyptiaca
Lygeum spartum
Plantago albicans
Reichardia tingitana
Retama raetam
Salsola tetrandra
Thymelaea hirsuta
Thymelaea microphylla
Steppe with Rhantherium suaveolens
Acacia saligna
Anacyclus monanthos subsp. Cyrtolepidioides
Apteranthes europaea [= Caralluma]
Artemisia campestris subsp. cinerea
Asparagus stipularis
Astragalus armatus subsp. tragacanthoides
Atractylis serratuloides
Cenchrus ciliaris
Centaurea dimorpha
Cistanche phelypaea
Deverra chlorantha [= Pituranthos tortuosa]
Echiochilon fruticosum
Eragrostis papposa
Kickxia aegyptiaca
Launaea mucronata [= L. resedifolia]
Lycium shawii
Lygeum spartum
Opuntia ficus-indica subsp. inermis
Peganum harmala
Picris coronopifolius
Polygonum equisetiforme
Reaumuria vermiculata
Retama raetam
Rhantherium suaveolens
Salsola villosa
Stipagrostis ciliata [= Aristida]
Vegetation of the Oases and beaches
Cakile maritima subsp. aegyptiaca
258
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
Centaurea contracta
Erodium arborescens
Frankenia pulverulenta
Globionis [= Chrysanthemum] coronarium
Hyoscyamus albus
Launaea resedifolia
Lotus creticus s. l.
Posidonia oceanica
Senecio glaucus subsp. coronopifolius
Silene succulenta
Tamarix sp.
White Sagebrush Steppe: (Artemisia herba-alba)
Ajuga iva subsp. pseudoiva
Anabasis oropediorum (2 pts poils)
Anacyclus monanthos subsp. cyrtolepidioides
Argyrolobium uniflorum [= Genista uniflora]
Artemisia campestris
Astragalus armatus
Astragalus caprinus
Atractylis carduus (Forssk.) C. Christ [= A. flava ],
Calendula aegyptiaca [= C. sancta]
Caralluma europaea
Carrichtera annua [= Vella annua]
Catananche arenaria
Convolvulus supinus
Cuscuta sp. sur Argyrolobium uniflorum
Deverra tortuosa
Didesmus bipinnatus Del.
Diplotaxis harra
Echium humile subsp. pycnanthos
Echium trygorrhizum
Erodium crassifolium [= E. hirtum]
Erodium glaucophyllum
Erodium pulverulentum
Fagonia cretica
Gymnocarpos decander Forssk.
Haloxylon scoparium Pomel [= Hammada scoparia]
Helianthemum kahiricum
259
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
Helianthemum virgatum
Herniaria fontanesii
Kickxia aegyptiaca [= Linaria]
Launaea resedifolia
Limonium pruinosum, accidental presence here!
Lycium shawii Roem. & Schult. [= L. arabicum]
Lygeum spartum
Matthiola longipetala
Muricaria prostrata
Pallenis hierochuntica [= Odontospermum pygmeum]
Paronychia arabica
Pistacia vera, roadside, planted, ground beetles are planted on the thorns, it
is a "shrike" "lardoir"!
Plantago ovata
Polygonum equisetiforme
Pteranthus dichotomus
Reaumuria vermiculata
Reichardia tingitana
Retama raetam
Rumex vesicarius
Salsola brevifolia
Salvia verbenaca
Seriphium herba-album [= Artemisia herba-alba ].
Stipa capensis (= S. tortilis)
Volutaria crupinoides
Volutaria lippii [= Amberboa lippii]
Vegetation of the Matmatas Mountains
Anagallis arvensis
Astragalus armatus
Bromus madritensis
Calicotome villosa .
Coris monspeliensis
Coronilla scorpioides
Dactylus glomerata subsp. hispanica
Deverra chloranthus
Didesmus bipinnatus
Ephedra altissima
Euphorbia cornuta
260
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
Gymnocarpos decander
Helianthemum intricatum
Helianthemum sessiliflorum
Helianthemum virgatum
Helichrysum stoechas
Hippocrepis ciliata ?
Rhus tripartita
Koelpinia linearis
Kickxia aegyptiaca
Lycium shawii
Lygeum spartum
Marrubium vulgare
Medicago minima
Moricandia arvensis
Onopordon espinae
Piptatherum miliaceum
Phagnalon rupestre
Pallenis hierochuntica
Pallenis spinosa
Papaver hybridum
Paronychia chlorothyrsa
Peganum harmala
Plantago albicans
Plantago ovata
Plantago psyllium
Pteranthus dichotomus
Reseda decursiva
Retama raetam
Rhus tripartita
Rosmarinus officinalis var. troglodytorum
Scandix pecten-veneris
Scilla peruviana
Scorzonera undulate
Seriphium herba-album
Sisymbrium erysimoides
Stipa tenacissima
Teucrium alopecurus
Thymelea hirsuta
261
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
Thymus capitatus
Thymus hirtus subsp. algeriensis
Trigonella stellata
Vaillantia sp.
Valerianella sp.
Steppe at Genista microcephala, near Tougène
Anabasis oropediorum
Astragalus armatus
Dittrichia viscosa [= Inula viscosa]
Genista microcephala
Plantago albicans
Plantago ovata
Ruta chalepensis
Stipa parviflora
Teucrium alopecurus
Vegetation of Foum Tatouine
Anacyclus clavatus
Anacyclus cyrtolepidioides
Anchusa hispida [= Gastrocotyle hispida]
Andrachne telephioides
Arnebia decumbens
Artemisia herba-alba
Asteriscus hierochuntica
Astragalus falciformis ?
Astragalus pseudosinaicus ?
Carrichtera annua
Cenchrus ciliaris [= Pennisetum]
Convolvulus supinus
Cuscuta sp.
Daucus sp.
Deverra chlorantha
Dipcadi serotinum
Diplotaxis harra
Echinops spinosus
Ephedra altissima
Erodium arborescens
Erodium crassifolium
Erodium pulverulentum var. tunetanum
262
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
Fagonia cretica
Filago germanica s. l.
Gymnarrhena micrantha
Gymnocarpos decander
Hammada scoparia
Helianthemum kahiricum
Lamarckia aurea
Lappula spinocarpos [= Sclerocaryopsis]
Matthiola kralikii
Moricandia arvensis
Papaver hybridum
Peganum harmala
Picris coronopifolia
Pinus halepensis
Plantago ovata
Pteranthus dichantomus
Rhanterium suaveolens
Reseda decursiva
Retama raetam
Rhus tripartita
Richardia tingitana
Scilla peruviana
Scorzonera undulata
S. glaucus subsp. coronopifolius
Sinapis alba
Stipa capensis
Stipa parviflora
Stipagrostis plumosa
Thesium humile
Trigonella polyceratia
Volutaria lippii
Steppe to Anthyllis henoniana, from Chenini
Aegilops triaristata
Allium roseum subsp.odoratissimum
Anthyllis sericea subsp.henoniana
Argylobium uniflorum
Artemisia herba-alba
Astragalus caprinus
263
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
Atractylis serratuloides
Bromus madritensis
Calendula arvensis
Convolvulus supinus
Cutandia dichotoma
Deverra chorantha
Diplotaxis harrra
Diplotaxis simplex
Echium trygorrhizum
Enarthrocarpus clavatus
Echiochilon fruticosum
Fagonia glutinosa
Gagea fibrosa
Gymnocarpos decander
Hedypnois cretica
Helianthemum crassifolium subsp. glaucum
Helianthemum intricatum
Helianthemum ledifolium
Herniaria fontanesii
Matthiola longipetala subsp. kralikii
Morea sisyrinchium [= Gynandriris]
Paronychia arabica subsp. cossoniana
Paronychia gr. kapela
Picris coronopifolia
Plantago albicans
Reaumuria vermiculata
Rostraria salzmannii
Scabiosa arenaria [= Sixalix arenaria]
Schismus barbatus
Scilla peruviana
Scorzonera undulata
Stipa capensis
Stipa parviflora
Stipa tenacissima
Tetrapogon villosus
Asparagus refractus
Asphodelus refractus
Calligonum polygonoides subsp. comosum
264
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
Cutandia dichotoma
Daucus sahariensis
Haloxylon schmittianum
Ifloga spicata
Koelpinia linearis
Salsola brevifolia
Stipagrostis pungens
Steppe to Stipagrostis pungens, by Ksar Ghilane
Anthyllis sericea subsp. henoniana
Asphodelus refractus
Centaurea furfuracea
Cutantia dichotoma
Daucus sahariensis
Gymnocarpos decander
Rhanterium suaveolens
Savigna parviflora subsp. longistyla
Stipagrostis pungens – Psammophile
whose roots clump together and fix the sand. These lateral ramifications can
follow the prevailing winds. They thus promote the development of
Rhanterium
Anthemis stiparum
Asphodelus tenuifolius
Atractylis carduus [= A. flava]
Cleome amblyocarpa
Helianthemum lippii var. sessiliflorum
Henophyton deserti [= Oudneya africana]
Koelpinia linearis
Matthiola longipetala
Nolletia chrysocomoides
Savignya parviflora subsp. longistyla
Stipagrostis pungens
Steppe to Euphorbia guyoniana, by Ksar Ghilane
Anthemis stiparum
Asphodelus tenuifolius
Astragalus hamosus
Astragalus saharae
Centaurea purpurea
Cutandia divaricata
Erodium chevallieri Guitt. [= E. glaucophyllum var. cinerascens Chevallier]
265
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
Euphorbia guyoniana
Herniaria fontanesii
Koelpinia linearis
Launaea capitata [= L. glomerata]
Lotus pusillus [= L. halophilus]
Plantago ciliata
Savignya parviflora subsp. longistyla Boiss
Vulpiella stipoides
Dunes in Ephedra alata, south of Douz
Anabasis articulata
Bassia muricata
Cistanche violacea
Ephedra alata subsp. alenda
The presence of this chlamydosperm species is the main feature of the
resort. For the alenda subspecies, the fruiting cones are 10-16 mm, with
bracts without tab at the base, male flowers with 6-7 anthers are grouped
into a dense head (Ozenda, 2004). It is common throughout Western Sahara.
Halocnenum strobilaceum
Haloxylon schmittianum Pomel
Helianthemum confertum Dun.
Ifloga spicata
Limoniastrum guyonianum
Lotus pusillus
Maresia nana
Moltkiopsis ciliata
Retama raetam
Senecio gallicus
Traganum nudatum
Zygophyllum album
et à 4 km au sud de Douz :
Calligonum polygonoides subsp. comosum
Casuarina equisetifolia
Salsola brevifolia
Suaeda mollis
Tamarix africana
Planting of "saxoul" Haploxylon persicum
Acacia karroo
Anabasis articulata
Arnebia decumbens
266
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
Diplotaxis harra
Erucaria vesicaria
Haloxylon persicum (introduit en 1969 par
Schoenenberger to fix the dunes: currently in the process of invasive
expansion.
Ifloga spicata
Launaea resedifolia
Maresia nana
Matthiola longipetala subsp. kralickii
Plantago albicans subsp. laniginosa
Reaumuria vermiculata
Senecio gallicus subsp. coronopifolius
Tamarix amplexicaulis [= T. pauciovulata]
Traganum nudatum
Zygophyllum album
Vegetation of the Edge of the Chotts (chott El Djerid, de Douz)
Cistanche violacea
Halocnemum strobilaceum
Limoniastrum guyonianum
Salsola tetragona
Tamarix africana
Zygophyllum album
Vegetation of the north-east of Tozeur
Aizoon canariense
Anabasis articulata
Asteriscus pygmaeus
Citrillus colocynthis [= Colocynthis vulgaris]
Echiochilon fruticosum
Filago pygmaea [= Evax pygmea]
Hammada schmittiana
Linaria laxiflora
Neurada procumbens
Peganum harmala
Polycarpaea repens
Retama raetam
Stipagrostis pungens
Tamarix gallica (cultivé)
Volutaria lippii
267
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
Other species of flora have been observed
Atriplex suberecta
Bassia indica
Bromus catharticus
Caesalpinia gilesii
Casuarina stricta [= quadrivalvis]
Cionura erecta
Fumaria capreolata
Fumaria mirabilis
Heliotropium currassavicum
Hordeum murinum
Hornungia procumbens
[= Hymenolobus procumbens]
Lawsonia inermis, le henné
Malva parviflora
Nicotiana glauca
Ocymum basilicum
Rubia tinctoria
Sphenopus divaricatus
Dunes in Calligonum arich (Grand Erg Oriental)
Calligonum arich
Astragalus gombiformis,
Calligonum. azel,
Cleome arabica,
Cornulaca monocantha,
Euphorbia gugoniana,
Helianthemum confertum,
Retama raetam,
Spartium saharae
Stipagrostis pungens
3. Results and discussion
The plant species identified during the visits to the study sites in the southern of Tunisia are represented by Figure 3.
Several studies have claimed that precipitation has a significant impact on the vegetation dynamics of arid zones [1920]. More particularly, rainfall variability has a great impact on plant phenology [21–22], plant life cycles [23–24], and
therefore species richness [25–26]. Rainfall distribution and quantity play important roles in encountering the
maximum number of plant species that can grow in arid and desert zones.
268
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
The favourable conditions of 2009/2008 resulted in a large number of plant species . Many of which were not recorded
in recent decades, such as Helianthemum crassifolium, Helianthemum ruficomum, Helianthemum virgatum subsp.
africanum, Plantago afra, Dactylis glomerata, Andrachne telephioides, Catananche arenaria, Coris monspeliensis, and
Teucrium alopecurus.
Concerning the floristic composition of the five chosen sites of tataouine, the altered climate conditions in the south of
Tunisia were associated with increased species richness. a total of 558 species were recorded, belonging to 58 families
(Table 2). The families with the highest number of species were Asteraceae with 86 species (30.70%), Poaceae with 60
(22%), Fabaceae with 48 (17.14%), Amaranthaceae with 32 (11.42%), Brassicaceae with 32 (11.42%), and
Boraginaceae, Caryophyllaceae, and Lamiaceae with 24species each (8% each). These families were the most diverse of
the flora in the arid zones of Tunisia. Overall, 54% of the species were annual (301 species) and 46% were perennial
(257). Several annual plant species can be found exclusively in improved microsite conditions (e.g., lower temperatures,
reduced solar radiation, or increased organic matter) in Rocky Mountains and benefit from higher rainfall. For example,
the presence of Lamarckia aurea and Umbilicus rupestris indicates favorable environmental conditions, which may be
the result of available microsites for plant establishment under higher rainfall conditions.
During the extremely wet year, the arid and desert rangelands, with all their different habitats (mountain, plain, wadi,
dune), tended to be dominated by therophytes (ephemerals and annuals) [27].
These species germinate on conditions that are favorable and thrive under heavy rainfall.
The life-form spectrum of these recorded species showed that 48% were therophytes, 20% were chamaephytes, 20%
were hemicryptophytes, 5% were nanophanerophytes, 3% were geophytes, 2% were macrophanerophytes, 1% were
phanerophytes, and 1% were parasites (Figure 4). The dominance of therophytes can be attributed to the large number
of microsites suitable to annual plants that have rapid germination and growth, thus increasing their abundance [46–
48]. Chamaephytes can survive in arid zones because they are highly adapted to arid conditions [28–29].
Figure 4 Life form distribution of plant species in the arid and desert zones of Tataouine, Tunisia (spring 2008).
The perennial shrubs were mainly chamaephytes, such as Haloxylon schmittianum, Haloxylon scoparium, Helianthemum
kahiricum, Helianthemum lippii, Rhanterium suaveolens, and Gymnocarpos decander, which characterize the dry and
desert rangelands. Hemicryptophytes were very common plants in large areas of arid rangelands, with more than some
species, most of which were Poaceae that emerge from seeds and propagate vegetatively from plant parts [30].
During the rainy season, the growth of herbaceous plants in the rangelands of Tataouine was very important (Figure 5).
Herbaceous vegetation was dominant, with 73% of species, followed by shrubs 25%, and trees 2%, with climbers
represented by only one species: Convolvulus supinus. Not surprisingly, herbaceous species were very abundant because
the majority of herbaceous species are therophytes and hemicryptophytes, which dominate the rangelands.
269
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
Figure 5 Habitat class of plant species in the arid and desert zones of Tataouine, Tunisia (spring 2008).
The inventoried rangelands had a relatively high species richness, due to its diverse plant communities combined with
favorable rainfall conditions.
Additionally, rangelands are characterized by a large number of palatable species belonging to Poaceae, such as Oloptum
miliaceum, Dactylis glomerata, Stipagrostis plumosa, Cynodon dactylon, and Cenchrus ciliaris. Annual plants that grow
mainly in spring are an important component of arid rangelands. They include, for example, many species that are very
palatable, such as Astragalus asterias, Astragalus hamosus, Astragalus arpilobus, Sulla carnosa, Hippocrepis areolata, and
Medicago laciniata of the Fabaceae. Moreover, in addition to its pastoral value, these rangelands have many valuable
medicinal and aromatic plants [31]. Many traditional species remedies derived from pastoral plants that originated in
natural rangelands have become modern medicines.[32] These species include the following : Allium roseum, Allium
ampeloprasum, Searsia tripartita, Periploca angustifolia, Capparis spinosa, Herniaria fontanesii, Haloxylon scoparium,
Artemisia herba-alba, Artemisia campestris, Henophyton deserti, Diplotaxis harra, Citrullus colocynthis,Calligonum
comosum, Ephedra alata, Ephedra altissima, Hyparrhenia hirta, Rosmarinus officinalis, Thymus algeriensis, Thymbra
capitata, Ajuga iva, Daucus carota, Marrubium deserti, Teucrium polium, Calicotome villosa, Retama raetam, Cymbopogon
schoenanthus, Calligonum polygonoides, Polygonum equisetiforme, Ziziphus lotus, Thymelaea hirsuta, Thapsia garganica,
Deverra denudata, Deverra tortuosa, Nitraria retusa, Peganum harmala, and Zygophyllum album. Some species have high
culinary value [33], such as Rosmarinus officinalis, Thymus algeriensis, Capparis spinosa, Allium roseum, and Allium
ampeloprasum. Some species, such as Ziziphus lotus and Nitraria retusa, have small edible fruits used by the local
population [34]. A few species are poisonous or toxic to animals, such as Peganum harmala, Euphorbia terracina,
Euphorbia retusa, and Adonis microcarpa.
The floristic survey conducted on the study sites revealed a high number of endangered species. The endangered forage
species were Anabasis oropediorum, Anarrhinum fruticosum, Calligonum comosum, Echiochilon fruticosum, Eragrostis
papposa, Sulla carnosa, Stipa parviflora, and Stipa lagascae. Likewise, the majority of the medicinal plants are considered
seriously threatened due to overuse. For example, Allium roseum is threatened with extinction because of
overexploitation; the harvesting of this plant is very destructive because the bulbs are torn off during harvesting [35].
Of the medicinal species recorded in our survey, eight are classified as critically endangered: Allium roseum, Allium
ampeloprasum, Ephedra alata, Ephedra altissima, Rosmarinus officinalis, Thymus algeriensis, Thymbra capitata, and
Cymbopogon schoenathus. Out of the 558 species that have been identified, some species are endemic to the country,
which are Anarrhinum fruticosum subsp. brevifolium,Calligonum arich, Helianthemum virgatum subsp. africanum,
Limonium tunetanum, Onopordum espinae, and Teucrium Alopecurus [36]. This inventory has devoted a great deal of
attention to the botanical composition and species diversity of arid and desert rangelands in Tataouine that provide
important ecosystem services, yet they are still neglected.
Nevertheless, a great number of plant species are still vitally important for human health, as well as livestock and
wildlife feeding. The recorded wide range of species reflects the significant resilience and adaptation of these arid
rangeland ecosystems. Among the strategies adopted by the arid plants to overcome such harsh conditions is their
270
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
ability to go dormant and cope with extreme heat and recurrent drought to ensure that neither internal temperatures
nor tissue dehydration reach low levels [36].
The degree of floristic importance varies from one species to another and is based on spatial distribution across the
region. Interesting enough, south Tunisia’s flora includes some species endemics to the country that are classified as
endangered.
There is solid evidence that greater botanical diversity is essential to sustainable land use by increasing forage yield,
pollinators, as well as weed and pest suppression [37]. Certainly, high botanical diversity also plays a key role in soil
aggregate stability. The root system of the plant improves soil structure and increases the soil organic matter [38-39].
Furthermore, plant diversity and root traits also benefit essential soil physical properties [38-39]. In recent years,
advanced research in ecological conservation, combined with greater focus on ecosystem services, have enhanced our
understanding of these complex ecosystems but also highlighted several challenges, calling for innovative measures to
preserve our natural resources.
4. Conclusion
In addition to the ecological importance of safeguarding the stability of the natural environment, the rich and diverse
flora of arid and desert rangelands in Tunisia provide essential ecological services to the livestock and human
population. They provide a great variety of native forage and medicinal plants with modern pharmacological uses.
Because the rangelands are not protected, a serious threat to floral diversity, caused by human activity, has occurred in
a large area of the arid rangelands, while climate conditions are creating significant transformation through favorable
years.
Although the rangelands of Tataouine are dry, they are the native habitat of more than 10% of the total flora of Tunisia.
The recorded species are mainly annuals and perennials characteristic of dry ecosystems. The main families are the
Asteraceae, Poaceae, Fabaceae, Amaranthaceae, Brassicaceae, Boraginaceae, Caryophyllaceae, Lamiaceae, Apiaceae, and
Cistaceae, which together account for 65% of the flora. Therophytes comprised the highest number of species, followed
by chamaephytes and hemicryptophytes. These rangelands are rich in foraging. Species of high nutritional value for
livestock feeding and many important plants used in both traditional and modern medicine. Despite this significant
floristic richness, certain species remain endangered and must be effectively managed and protected to avoid their
extinction. For this, it is necessary to set up a comprehensive biodiversity conservation program. Furthermore, it would
be wise to establish botanical gardens or field gene banks as part of a long-term biodiversity conservation program for
endangered species.
Compliance with ethical standards
Acknowledgments
Acknowledgments:I thank the research team of the Institute of Arid Regions of Medenine (Tunisia) research for the help
I have received.
Conflicts of Interest
The authors declare no conflict of interest References
References
[1]
[2]
Le Floc’h E. Contribution à une étude ethnobotanique de la Flore Tunisienne; Imprimerie Officielle de la
République Tunisienne: Tunis, Tunisia, 1983.
Le Houérou HN. Recherches écologiques et floristiques sur la végétation de la Tunisie méridionale. Institut des
Recherches Sahariennes, Alger. Le Houérou, H.N., 1995. Bioclimatologie.1959.
[3]
He J, Yan C, Holyoak M Wan X, Ren G, Hou Y, Xie Y, Zhang Z. Quantifying the effects of climate and anthropogenic
change on regional species loss in China. PLoS ONE 2018; 13: e0199735.
[4]
Sala OE Global biodiversity scenarios for the year 2100. Science 2000; 287: 1770–1774
271
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
[5]
Hudson LN, Newbold T, Contu S, Hill SLL, Lysenko I, De Palma A, Phillips HRP, Senior RA, Bennett DJ, Booth H, et
al. The PREDICTS database. A global database of how local terrestrial biodiversity responds to human impacts.
Ecol. Evol. 2014; 4: 4701–4735.
[6]
Ouled Belgacem A, Louhaichi M. The vulnerability of native rangeland plant species to global climate change in
the West Asia and North African regions. Climat. Chang. 2013; 119: 451–463.
[7]
Louhaichi M, Ouled BA, Hassan S, Petersen LS. Effects of climate change and grazing practices on shrub
communities of West Asian rangelands. Int. J. Clim. Change Str. Manag. 2019; 11: 660–671.
[8]
Fensham RJ, Silcock JL, Dwyer JM. Plant species richness responses to grazing protection and degradation history
in a low productivity landscape. J. Veg. Sci. 2011; 22: 997–1008.
[9]
Mönkkönen M. Managing Nordic boreal forest landscapes for biodiversity: Ecological and economic perspectives.
Biodivers. Conserv. 1999; 8: 85–99.
[10]
Tarhouni M, Ben Hmida W, Ouled Belgacem A, Louhaichi M, Neffati M. Is long-term protection useful for the
regeneration of disturbed plant communities in dry areas? Afr. J. Ecol. 2017; 55: 509–517.
[11]
Gamoun M, Ouled Belgacem A, Louhaichi M. Diversity of desert rangelands of Tunisia. Plant Divers. 2018; 40:
217–225.
[12]
Ouled Belgacem A, Ben Salem F, Gamoun M, Chibani R, Louhaichi M. Revival of traditional best practices for
rangeland restoration under climate change in the dry areas: A case study from Southern Tunisia. Int. J. Clim.
Chang. Strateg. Manag. 2019; 11: 643–659.
[13]
Meir E, Andelman S, Possingham HP. Does conservation planning matter in a dynamic and uncertain world? Ecol.
Lett. 2004; 7: 615–622.
[14]
ODS. Tataouine Governorate in Numbers; Republic of Tunisia Ministry of Development, Investment and
International Cooperation, Southern Development Office: Tunis, Tunisia. 2018.
[15]
Pottier-Aiapetite G. Flore de la Tunisie: Angiospermes, Dicotyledones Apetales-Dialypetales; Ministère de
l’Enseignement Supérieur et de la Recherche Scientifique et le Ministère de l’Agriculture: Tunis, Tunisia, 1979;
1–654.
[16]
Pottier Alapetite G. Flore de la Tunisie: Angiospermes-Dicotylédones, Gamopétales. Programme Flore et
Végétation Tunisiennes; Ministère de l’Enseignement Supérieur et de la Recherche Scientifique et le Ministère de
l’Agriculture: Tunis, Tunisia, 1981.
[17]
Dobignard A, Chatelain C. Synonymic and Bibliographical Index of the Flora of North Africa; Conservatoire et
Jardin Botaniques de la Ville de Genève: Geneva, Switzerland. 2010–2013.
[18]
POWO. Plants of the WorldOnline. Facilitated by theRoyal BotanicGardens,Kew. Available online:
http://www.plantsoftheworldonline.org/2020 (accessed on 11 February 2021).
[19]
CRDA. Tataouine. Commissariat Régional au Développement Agricole de Tataouine: Tunis, Tunisia.
[20]
Yan H, Liang C, Li Z.; Liu, Z.; Miao, B.; He, C, Sheng L. Impact of precipitation patterns on biomass and species
richness of annuals in a dry steppe. PLoS ONE 2015; 10, e0125300
[21]
García-Vega D, Newbold T. Assessing the effects of land use on biodiversity in the world’s drylands and
Mediterranean environments. Biodivers. Conserv. 2019; 29: 393–408.
[22]
Mathias A, Chesson P. Coexistence and evolutionary dynamics mediated by seasonal environmental variation in
annual plant communities. Theor. Popul. Biol. 2013; 84: 56–71.
[23]
Richardson AD, Keenan TF, Migliavacca M, Ryu Y, Sonnentag O, Toomey M. Climate change, phenology, and
phonological control of vegetation feedbacks to the climate system. Agric. For. Meteorol. 2013; 169: 156–173.
[24]
Loeser MRR, Sisk TD, Crews TE. mpact of grazing intensity during drought in an Arizona grassland. Conserv. Biol.
2007; 21: 87–97.
[25]
Li J, Lin S, Taube F, Pan Q, Dittert K. Above and belowground net primary productivity of grassland influenced by
supplemental water and nitrogen in Inner Mongolia. Plant Soil 2011; 340: 53–64.
[26]
Holzaphel C, Schmidt W, Shmida A. Effects of human-caused distribution on the flora along a Mediterraneandesert gradient. Flora 1992; 186: 261–270.
272
GSC Biological and Pharmaceutical Sciences, 2022, 18(03), 250–273
[27]
Kinugasa T, Tsunekawa A, Shinoda M, Increasing nitrogen deposition enhances post-drought recovery of
grassland productivity in the Mongolian steppe. Oecologia 2012; 170: 857–865.
[28]
Gamoun M. The Impact of Rest from Grazing on Vegetation Dynamics: Application to Sustainable Management of
Saharan Rangelands in Southern Tunisia. Ph.D. Thesis, University of Tunis El Manar, Tunis, Tunisia, 2012.
[29]
Kahmen S, Poschlod P. Effects of grasslandmanagement on plant functional trait composition. Agric. Ecosyst.
Environ. 2008; 128: 137–145.
[30]
Gamoun M, Ouled Belgacem, A, Hanchi, B, Neffati M, Gillet F. Impact of grazing on the floristic diversity of arid
rangelands in South Tunisia. Rev. Ecol. 2012; 67: 271–282.
[31]
Neffati M, Najjaa H, Máthé A. Medicinal and Aromatic Plants of the World—Africa; Springer Nature:
Berin/Heidelberg, Germany. 2017; (3).
[32]
Chaieb M, Boukhris M. Flore Succinte et Illustrée des Zones Arides et Désertiques de Tunisie; Association pour la
Protection de la Nature et de l’Environnement. Sfax, Tunisia, 1998.
[33]
Jendoubi R, Neffati M, Henchi B, Yobi A. Système de reproduction et variabilité morphologique chez Allium
roseum L. Plant Genet. Res. Newsl. 2001; 127: 29–34.
[34]
Neffati, M.; Ghrabi-Gammar, Z.; Akrimi, N.; Henchi, B. Les plantes endémiques de la Tunisie. Flora Mediterr. 1999;
9: 163–174.
[35]
Laity J. Deserts and Desert Environments; JohnWiley & Sons, Inc. Hoboken, NJ, USA. 2008.
[36]
Isbell F, Adler PR, Eisenhauer N, Fornara D, Kimmel K, Kremen C, Letourneau DK, Liebman M. Polley HW. Quijas
S. et al. Benefits of increasing plant diversity in sustainable agroecosystems. J. Ecol. 2017; 105:871–879.
[37]
Gould IJ, Quinton JN, Weigelt A, De Deyn GB, Bardgett RD. Plant diversity and root traits benefit physical
properties key to soil function in grasslands. Ecol. Lett. 2016; 19: 1140–1149.
[38]
Aronson, C Floret, E Le Floc'h, C Ovalle, R Pontanier. Restoration and Rehabilitation of Degraded Ecosystems in
Arid and Semi-Arid Lands. II. Case Studies in Southern Tunisia, Central Chile and Northern Cameroon Restoration
Ecology 1993; 1(3):168-187.
[39]
Adel Dhief, Mustapha Gorai, Samira Aschi-Smiti, Mohamed Neffati; Comparative phenological and water potential
patterns of three Calligonum species in the eastern great Erg of Tunisia. 2009;204: 581–592, Flora.
273