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International Journal of Mediterranean Ecology - Ecologia ...

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ADEL DHIEF, MUSTAPHA GORAI, SAMIRA ASCHI-SMITI, MOHAMED NEFFATI<br />

20<br />

mination des graines non traitées et le trempage<br />

dans l’acide sulfurique (96 %) pendant<br />

30 minutes était le plus efficace pour lever la<br />

dormance des graines et augmenter par conséquent<br />

le pourcentage de germination des trois<br />

espèces de Calligonum.<br />

Introduction<br />

The Calligonum genus belongs to the Polygonaceae<br />

family, represented by 60-80 species<br />

(Singh 2004; Okasaka et al. 2004) distributed<br />

throughout Western Asia, Southern Europe,<br />

and North Africa. In Tunisia, the genus Calligonum<br />

is represented by three species:<br />

C. comosum L’Hérit., C. azel Maire and<br />

C. arich Le Houérou (Le Houérou 1959;<br />

Dhief et al. 2009). These species are dominant<br />

perennials in active sand dunes and stabilized<br />

sand field in Southern desert <strong>of</strong><br />

Tunisia and grow naturally in Eastern Great<br />

Erg existing in different dune slope positions<br />

(Dhief et al. 2009). They are considered the<br />

most important woody species in the Saharan<br />

zone <strong>of</strong> Tunisia (Aronson et al. 1993). They<br />

are used for fuel and charcoal production by<br />

local nomadic populations; the overuse in this<br />

respect has contributed to their decrease (Le<br />

Houérou 1959; Pottier-Alapetite 1979;<br />

Auclair & Zaafouri 1996).<br />

Dhief et al. (2009), showed that C. comosum<br />

existing in the interdune sites ends all growth<br />

activity in June, while C. azel and C. arich<br />

existing in the dune slope crests extend the<br />

period <strong>of</strong> their vegetative growth into the<br />

months <strong>of</strong> low rainfall (July and August). The<br />

flowering starts in March for C. azel and<br />

C. comosum, while starting in April for<br />

C. arich. The time period between the beginning<br />

<strong>of</strong> flowering and mature fruit production<br />

is approximately six weeks for all the three<br />

species (Dhief et al. 2009). The seed germination<br />

starts following the first rains <strong>of</strong><br />

Spring. The seed phase is arguably the most<br />

important stage <strong>of</strong> the higher plant life cycle,<br />

ensuring species survival. Most seeds are well<br />

equipped to survive for long periods <strong>of</strong><br />

unfavourable conditions before germination<br />

and to give plants in the most favourable conditions.<br />

Seeds temporarily fail to germinate in<br />

conditions that might be adequate for germination<br />

(Baskin & Baskin 1998).<br />

The forest seed plays a key role in breeding<br />

and regenerating (Fan & Li 2004). Because<br />

the great majority <strong>of</strong> seeds has a dormancy<br />

phenomenon, the research about dormancy<br />

and its determination is important. Physiological<br />

seed dormancy (PD) is the most widespread<br />

dormancy class <strong>of</strong> the new ecological<br />

classification system proposed by Baskin &<br />

Baskin (2004) which provides a comprehensive<br />

ecological description <strong>of</strong> the ‘wholeseed’<br />

dormancy response.<br />

Physiological seed dormancy is present<br />

throughout the plant kingdom and has a pr<strong>of</strong>ound<br />

impact on the structure and development<br />

<strong>of</strong> plant communities across all major<br />

climatic regions (Cohn 1996; Hilhorst 1997).<br />

Baskin & Baskin (1998, 2004) have proposed<br />

a comprehensive classification system including<br />

five categories <strong>of</strong> seed dormancy: physiological<br />

(PD), morphological (MD), morphophysiological<br />

(MPD), physical (PY) and<br />

combinational (PY + PD).<br />

Seed coat hardness and impermeability to<br />

water may be the most important causes <strong>of</strong><br />

Calligonum spp. dormancy (Yu & Wang<br />

1998; Tao et al. 2000; Ren & Tao 2004). Several<br />

pre-sowing treatments have been proposed<br />

for reducing seed hardness and improving<br />

the germination rate <strong>of</strong> the other species<br />

<strong>of</strong> the same genus (Ren & Tao 2004). Baskin<br />

& Baskin (1998) reported that physical and<br />

physiological dormancies are equally important<br />

among desert shrubs.<br />

Although the three Calligonum species have<br />

shown a great potential to provide different<br />

products and services and a wide adaptability<br />

to a large range <strong>of</strong> environmental conditions<br />

(Dhief et al. 2009), little information is available<br />

in literature on seed germination characteristics<br />

and techniques for breaking its coatimposed<br />

dormancy.<br />

There has been little experimental research<br />

done on the Tunisian Calligonum species and<br />

we tried to investigate the factors controlling<br />

seed germination. This study was conducted<br />

to better understand seed germination <strong>of</strong> the<br />

three Calligonum species occurring under the<br />

arid-type climate in the Eastern Great Erg <strong>of</strong><br />

Tunisia by comparing different pre-sowing<br />

seed treatments (mechanical, physical and<br />

chemical scarifications) as practical methods<br />

to break seed dormancy and enhance germination.<br />

Information from this study provided<br />

basic knowledge about germination that can<br />

be used for re-establishing projects.<br />

ecologia mediterranea – Vol. 38 (1) – 2012

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