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Ecologia Mediterranea

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N. BOUCHENEB, S.S. BENHOUHOU<br />

78<br />

Discussion<br />

The described associations clearly relate to<br />

the altitudinal and edaphic factors at work in<br />

the different wadi types of the Tamanrasset<br />

region. Climatic factors are important in<br />

determining large scale patterns of species<br />

distribution while factors such as topography<br />

and edaphic conditions are more important in<br />

determining vegetation patterns at a smaller<br />

spatial scale (Kadmon & Danin 1999). The<br />

importance of altitude as a major ecological<br />

gradient, which has been shown to affect<br />

species distribution in mountainous regions of<br />

the Saharo-Arabian belt, is an obvious consequence<br />

of the correlation between increased<br />

altitude and higher rainfall (Abd El-Ghani<br />

1996; Danin et al. 1975; Deil 1998; Moustafa<br />

& Klopatek 1995). Altitude is thus here considered<br />

as a “proxy” parameter for explaining<br />

rain variation. Several studies in desert<br />

regions highlight the importance of elevation,<br />

topography, soil texture and water availability<br />

in identifying plant communities and<br />

among others one can mention the desert of<br />

Dubai (Deil & Müller-Hohenstein 1996), the<br />

desert mountains of Oman (Brinkmann et al.<br />

2009), the desert mountains of Yemen (Deil<br />

& Müller-Hohenstein 1985), the Negev desert<br />

of Israel (Danin 1999), Sinai in Egypt<br />

(Moustafa & Klopatek 1995; Moustafa &<br />

Zaghloul 1996) and the Eastern Desert of<br />

Egypt (Abd El-Ghani 1998).<br />

When considering the described associations<br />

in the Tamanrasset region in a wider geographical<br />

context, the isolation of the central<br />

Sahara Mountains in the Saharo-Arabian belt<br />

appears to be a strong factor in leading to the<br />

development of distinctive plant communities.<br />

This is particularly clear with our most alticolous<br />

community, that is: Rhus tripartita-<br />

Olea europaea subsp. laperrinei association.<br />

It is clearly a distinctive association, for which<br />

similar communities in other mountainous<br />

area of the Saharo-Arabian belt are difficult<br />

to find, with the exception of the nearby Air<br />

Mountains, south of the Ahaggar, where common<br />

species such as Rhus tripartita, Rumex<br />

vesicarius L., Senecio spp. and Lavandula<br />

antineae have high frequencies (Anthelme et<br />

al. 2007).<br />

With regard to the Acacia communities, gravelly-sandy<br />

wadis bear the Acacia-Panicum<br />

desertic savannah which is present with several<br />

variants throughout the Sahara (Leonard<br />

2001).<br />

The three associations described in the present<br />

study fit into the Pergulario-Pulicarietea<br />

Quézel 1965, while those in other parts of the<br />

Saharo-Arabian belt are related to the Acacietea<br />

tortilis, which is of East Sudanese distribution<br />

(Deil & Müller-Hohenstein 1985).<br />

Dominant species are the same as those found<br />

in our Acacia communities such as: Acacia<br />

tortilis subsp. raddiana, Acacia ehrenbergiana,<br />

Balanites aegyptiaca, Calotropis procera(Aiton)<br />

W.T. Aiton, Leptadenia pyrotechnica,<br />

Maerua crassifolia, Panicum turgidum<br />

and Zilla spinosa (Abd El-Ghani & Ameur<br />

2003; Ali et al. 2000; Boulos 2008; Shaltout<br />

& Mady 1996; Springuel et al. 1991). Where<br />

relief and substrate are similar, vicarious communities<br />

are well represented across the<br />

whole Saharo-Arabian belt. The Cassia<br />

aschrek-Panicum turgidum association resembles<br />

several communities. In the Hazeva area<br />

of the Negev Desert, Rudich and Danin<br />

(1978) describe a pseudo-savannah of Acacia<br />

tortilis subsp. raddiana associated with<br />

Haloxylon scoparium Pomel and Anabasis<br />

articulata. In the Eastern and Western Desert<br />

of Egypt Acacia raddiana Savi communities<br />

form well defined associations with Tetraena<br />

coccinea (L.) Beier & Thulin (Abd El-Ghani<br />

et al. 2003; Bornkamm & Kehl 1990; Boulos<br />

2008) and Zilla spinosa (Springuel et al.<br />

1991).<br />

The Acacia tortilis subsp. raddiana-Salvadora<br />

persica association is vicarious to the<br />

Acacia ehrenbergiana-Salvadora persica<br />

community found on silty wadis of the<br />

Tihama Mountains in Yemen at altitudes<br />

between 240 and 400 m (Deil & Müller-<br />

Hohenstein 1985).<br />

With regard to the Leptadenia pyrotechnica-<br />

Chrozophora brocchiana association, a similar<br />

community, the Acacia raddiana subsp.<br />

tortilis-Leptadenia pyrotechnica association,<br />

with the same new name that we propose for<br />

our association, is recorded by Abd El-Ghani<br />

& Amer (2003) from alluvial fans along the<br />

Gulf of Suez in the Sinai desert.<br />

The Tamarix aphylla-Farsetia ramosissima<br />

association found on very large wadi beds is<br />

vicarious to several communities found in<br />

similar ecological conditions of the Saharan-<br />

Arabian belt. The closest vicarious community<br />

is probably the Acacia raddiana-Tamarix<br />

nilotica found on main channels of large<br />

wadis in the Hazeva area in the Negev where<br />

three trees are dominant: Acacia tortilis<br />

subsp. raddiana, Balanites aegyptiaca and<br />

ecologia mediterranea – Vol. 38 (2) – 2012

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