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International Journal of Mediterranean Ecology - Ecologia ...

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

26<br />

events during the germination <strong>of</strong> Lepidium<br />

sativum L. and Arabidopsis thaliana (L.)<br />

Heyhn. Abscisic acid (ABA) specifically<br />

inhibits the endosperm rupture <strong>of</strong> these two<br />

closely related Brassicaceae species. In PD<br />

seeds, the embryo-covering layers can confer<br />

mechanical constraint (coat dormancy) that<br />

must be overcome by the growth potential <strong>of</strong><br />

the embryo (Bewley 1997; Koornneef et al.<br />

2002; Leubner-Metzger 2003; Kucera et al.<br />

2005). C. arich has larger seeds than C. comosum<br />

and C. azel. Experimentally, large seeds<br />

have an advantage over small seeds by having<br />

greater nutrient reserves for the young<br />

seedlings to enable them to grow larger and<br />

to tap resources earlier (e.g., water, sunlight,<br />

mineral nutrients). Thus, seedlings from<br />

large-seeded species could establish under a<br />

range <strong>of</strong> environmental conditions that could<br />

not be tolerated by seedlings from smallseeded<br />

species, notably competition for<br />

resources, and the capricious drought prone<br />

environments (Westoby et al. 2002; Moles &<br />

Westoby 2004). Seed age has been demonstrated<br />

to be related to seed mass in that<br />

smaller seeds can remain viable (in seed<br />

banks) over longer periods than larger seeds<br />

(Leishman et al. 2000). C. comosum has a<br />

greater seed dry mass than C. arich and C.<br />

azel. The difference in the rate <strong>of</strong> imbibition<br />

among Calligonum species is largely a function<br />

<strong>of</strong> seed dry mass and the density <strong>of</strong> seed<br />

seta (Zhang 1992). Variations between seed<br />

mass have been predicted to be <strong>of</strong> the greatest<br />

significance to the initial seedling establishment<br />

in arid zones (Susko & Lovett Doust<br />

2000). Information on seed germination is<br />

also important for the propagation <strong>of</strong> potentially<br />

and economically important desert plant<br />

species.<br />

Conclusion<br />

In conclusion, scarification treatments are one<br />

<strong>of</strong> the most effective methods for germinating<br />

Calligonum seeds. These experiments were<br />

conducted in order to find practical methods<br />

<strong>of</strong> seed treatment, which would improve the<br />

germination <strong>of</strong> the three dominant and economically<br />

important species widely distributed<br />

in the active sand dunes in Southern<br />

Tunisia. Chemical scarification for a minimum<br />

<strong>of</strong> 20 min significantly improved the<br />

germination <strong>of</strong> these species, suggesting that<br />

dormancy in these seeds might be due to the<br />

hardness and impermeability <strong>of</strong> the seed coat.<br />

In the context <strong>of</strong> the potential use <strong>of</strong> Calligonum<br />

species as an alternative in the arid<br />

desert regions, it is our contention that seed<br />

germination and seedling emergence under<br />

the natural environmental conditions still<br />

deserve further research.<br />

References<br />

Aronson J., Floret C., Le Floc’h E., Ovalle C. & Pontanier<br />

R., 1993. Restoration and rehabilitation <strong>of</strong><br />

degraded ecosystems in arid and semi-arid lands. II.<br />

Case studies in southern Tunisia, central Chile and<br />

northern Cameroon. Restor. Ecol. 1: 168-186.<br />

Auclair L. & Zaafouri M.S., 1996. La sédentarisation<br />

des nomades dans le sud tunisien : comportements<br />

énergétiques et désertification. Sécheresse 7 : 17-24.<br />

Baskin C.C. & Baskin J.M., 1998. Seeds. <strong>Ecology</strong>, biogeography,<br />

and evolution <strong>of</strong> dormancy and germination.<br />

Academic Press, San Diego.<br />

Baskin J.M. & Baskin C.C., 2004. A classification for<br />

seed dormancy. Seed Sci. Res. 14: 1-16.<br />

Bewley J.D., 1997. Seed germination and dormancy.<br />

Plant Cell. 9: 1055-1066.<br />

Bond W.J., Honig M. & Maze K.E., 1999. Seed size and<br />

seedling emergence: an allometric relationship and<br />

some ecological implications. Oecologia 120: 132-<br />

136.<br />

Chen R. & Fu J., 1984. Physiological studies on the seed<br />

dormancy and germination <strong>of</strong> Erythrophloeum<br />

fordii. Scientia Silvae Sinicae.<br />

Cohn M.A., 1996. Operational and philosophical decisions<br />

in seed dormancy research. Seed Sci. Res. 6:<br />

147-153.<br />

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seedling establishment <strong>of</strong> two desert shrubs, Calligonum<br />

polygonoides (Polygonaceae) and Spartidium<br />

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Acta Bot. Gallica 154 (4): 533-544.<br />

Dhief A., Gorai M., Aschi-Smiti S. & Neffati M., 2009.<br />

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Fan C. & Li X.W., 2004. The Dormancy <strong>of</strong> Forest Seed<br />

and it’s Termination. (Forestry and Horticulture College,<br />

Sichuan Agricultural University, Ya’an,<br />

625014, Sichuan), Sichuan Forestry Exploration and<br />

Design.<br />

Fenner M. & Thompson K., 2005. The ecology <strong>of</strong> seeds.<br />

Cambridge, UK: Cambridge University Press.<br />

Finch-Savage W.E. & Leubner-Metzger G., 2006. Seed<br />

dormancy and the control <strong>of</strong> germination. New phytol.<br />

171: 501-23.<br />

Gardarin A., Durr C., Mannino M., R. Busset H. & Colbach<br />

N., 2010. Seed mortality in the soil is related<br />

to seed coat thickness. Seed Sci. Res. 20: 243-256.<br />

Hilhorst H.W.M., 1997. Seed dormancy. Seed Sci. Res.<br />

7: 221-223.<br />

Institut national météorologique (INM), 1996. Fiche climatique<br />

des stations principales de la Tunisie. Rapports<br />

et publications, Tunis, Tunisie.<br />

ecologia mediterranea – Vol. 38 (1) – 2012

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