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Vol. 32 – 2006 - Ecologia Mediterranea

Vol. 32 – 2006 - Ecologia Mediterranea

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MOHAMED TARHOUNI, AZAIEZ OULED BELGACEM, BELGACEM HENCHI, MOHAMED NEFFATI<br />

40<br />

en fonction des distances par rapport aux puits<br />

alors que celui des thérophytes ne varie pas ; (3)<br />

au cours du printemps, les recouvrements des<br />

arido-passives et des arido-actives sont plus<br />

importants ; (4) le recouvrement des aridoactives<br />

augmente avec la distance par rapport<br />

aux puits mais celui des arido-passive ne varie<br />

pas ; (5) le recouvrement des CRS et celui des RS<br />

sont plus importants au cours du printemps et<br />

(6) les recouvrements des CS, des CRS et des S<br />

augmentent avec la distance par rapport aux<br />

puits à l’exception de celui des RS.<br />

Introduction<br />

Spontaneous plants are submitted to many<br />

constraints such as abiotic stress and human<br />

disturbance, particularly in arid environments.<br />

The harsh climatic conditions are high temperatures<br />

in summer and cool in winter. These<br />

inter-seasonal variations constitute an important<br />

thermal stress (Le Houerou 1995) and<br />

affect plant germination, a crucial stage in<br />

their establishment (Gilbert & Haferkamp<br />

1989). Water stress, which characterizes the<br />

arid bioclimates (including the <strong>Mediterranea</strong>n<br />

one), induces a decrease in the total dry<br />

weight and leaf area of plants, as well as in<br />

the dry weight and length of roots (Munns<br />

2002; Banon et al. 2004). Human activities<br />

and grazing pressure affect floristic diversity<br />

(Jauffret & Visser 2003; Mahamane & Mahamane<br />

2005; Tarhouni et al. <strong>2006</strong>). Grazing<br />

induces a change in the ecological balance<br />

because animals make a consumption choice<br />

which favors no consumed plants to the detriment<br />

of the appreciated ones (Waechter 1982;<br />

Boudet 1984).<br />

In southern Tunisia, characterized by elevated<br />

stresses and strong human disturbances, the<br />

flora is mainly constituted by resistant and<br />

adapted species. However, for most north-<br />

African steppic species, comparative and specific<br />

data describing plant adaptative strategies<br />

are rare, and the information in the<br />

regional flora books (Cuenod et al. 1954;<br />

Quezel & Santa 1962, 1963; Ozenda 1977;<br />

Pottier-Alapetite 1979, 1981) is insufficient to<br />

study these mechanisms. The combination of<br />

biologic types (life forms) in a biologic spectrum,<br />

sensu Raunkiaer (1934), corresponds to<br />

the analysis of vegetation structure and its<br />

biologic characters (Godron 1971). The biologic<br />

spectrum is considered as a flora adaptation<br />

strategy to environmental conditions<br />

especially to climatic ones (Daget 1980; Box<br />

1987). This spectrum is an ecosystem vital<br />

attribute and describes the structure and the<br />

function of ecological systems; usually the<br />

rank of life forms in the ecosystem decreases<br />

with the degradation degree (Aronson & Le<br />

Floc’h 1996). On the other hand, Evenari et<br />

al. (1975) proposed a classification permitting<br />

to assign species functional criteria in relation<br />

with their adaptation to the harsh climatic<br />

conditions. Indeed, these authors classified, in<br />

accordance with Noy-Meir (1973), the arid<br />

zone plant species in two categories: (i) the<br />

“arido-passive” species which do not possess<br />

a photosynthetic activity during the dry period<br />

and (ii) the “arido-active” species which<br />

maintain such activity, even reduced, during<br />

this period. The C-S-R Grime model completes<br />

the classification of plants to climatic<br />

constraints and human disturbances (Grime<br />

1974, 1977; Grime et al. 1988). This model<br />

classify plants to three groups: (1) Competitive<br />

(C) plants monopolizing resources with<br />

their strong vegetative development; (2)<br />

Stress-tolerant (S) plants occupying habitats<br />

poor in nutrients and (3) Ruderal (R) plants<br />

growing where the natural vegetational cover<br />

has been disturbed.<br />

In order to reduce the loss of plant diversity<br />

and the loss of ecosystem resilience, it is necessary<br />

to better understand and predict the<br />

behaviour of various response groups within<br />

plant communities (Aronson et al. 2002). It<br />

seems that the C-S-R model, extensively used<br />

by Grime and his collaborators to establish<br />

management plans and make restoration recommendations,<br />

determines vegetation<br />

response to all the abiotic and biotic changes.<br />

Grime’s concept is very attractive as it<br />

describes plant species adaptation in particular<br />

to their environment and along of disturbance<br />

and stress gradient (Jauffret 2001).<br />

However, the use of the CSR strategies, conceived<br />

on the herbaceous vegetation of temperate<br />

Europe, required an adapted interpretation<br />

to the north-African steppe because of<br />

the knowledge missing on the majority of its<br />

species (Jauffret & Visser 2003).<br />

In this study, we evaluate the influence of a<br />

disturbance gradient and of seasonal drought<br />

on plant species depending on their classification<br />

in various types. The aims are to understand:<br />

(i) What is the impact of seasonal<br />

drought and disturbance degree on species<br />

biologic spectrum (Raunkiaer 1934)? (ii)<br />

What is the impact of seasonal drought and<br />

ecologia mediterranea <strong>–</strong> <strong>Vol</strong>. <strong>32</strong> <strong>–</strong> <strong>2006</strong>

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