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162<br />

◆ L. M. M. BIDAK<br />

Value of correlations Seed mass<br />

Germination %<br />

Seed size<br />

Petri-dish<br />

-0.136<br />

0.031<br />

Half- water (HFC)<br />

0.024<br />

0.147<br />

Full water (FFC)<br />

-0.063<br />

0.096<br />

Number of Days of survival<br />

Petri- dish for annuals<br />

0.866** 0.470**<br />

Petri- dish for perennials<br />

0.520*<br />

0.371*<br />

Half-Water for annuals<br />

Half-Water for perennials<br />

and seed mass especially when water is available in the<br />

habitats (e.g. canal bank, fallow fields, wadi & catchment<br />

area). When availability of water decreased and habitats<br />

tend to be drier, no significant correlation is obtained<br />

(e.g. the inland plateau, saline depression, sand dunes and<br />

rocky cliffs). These results are confirmed by the correlation<br />

value between seed size and mass of plant species<br />

collected from the catchments areas, desert and railway<br />

roads, where occasional availability of water occurs<br />

depending on the rain or other sources.<br />

DISCUSSION<br />

0.700**<br />

0.194<br />

** Correlation is significant at the 0.01 probability level.<br />

* Correlation is significant at the 0.05 probability level.<br />

Table 5. Values of Pearson’s two-tailed correlation.<br />

0.587**<br />

0.348<br />

The size and shape of the studied seeds are extremely<br />

variable. These characteristics depend on the form of<br />

the ovary, the condition under which the parent plant is<br />

grown and obviously on the species. Other factors, which<br />

determine the size and the shape of seeds, are the size of<br />

the embryo and the amount of the endosperm. Several<br />

authors (e.g. Mott, 1972; Pate & McComb, 1981) have<br />

argued that the germination events in arid and semi-arid<br />

regions are triggered by large rainfall events and so the<br />

developing seedlings may not face water stress for some<br />

time. Many species showed adaptations to ensure germination<br />

only under favorable soil moisture conditions and<br />

may have characteristics such as mucilaginous gel or hairs<br />

which improve the soil-seed contact to maximize water<br />

uptake (Pate & McComb, 1981).<br />

Habitats can be classified along a spectrum from<br />

environments permitting fast growth rate to environments<br />

permitting only slow growth rate, due to low soil<br />

nutrients or moisture or to other impediments to plant<br />

growth. Species occupying slow growth habitats tend to<br />

have naturally slow relative growth rate even when given<br />

favorable conditions (e.g. Grime, 1974, 1977; Chapin,<br />

1980, 1991). In the present study, results of germination<br />

and growth performance of the plant species collected<br />

from the saline and inland plateau habitats revealed that<br />

seedling growth, emergence, germination and establishment<br />

of seeds were more affected than those collected<br />

from other habitats. This may be attributed to the stressful<br />

effect of the habitat and this seems to be in agreement<br />

with the finding trend suggested by Grime (1974, 1977)<br />

and Chapin (1980, 1991).<br />

Resources in the embryo and endosperm of a seed<br />

are deployed during germination to construct a seedling.<br />

Different plant species provision their seeds with different<br />

quantities of resources to support seedling establishment.<br />

Species span a range of seed mass from less than 10 -6<br />

to more than 10 4 g (Harper, 1977). Differences across<br />

species in seed coat thickness, dispersal structures, water<br />

contents and mineral nutrient concentrations reflect a<br />

wide range in the dry mass of resources provided by<br />

the mother plant to each of its offspring (Westoby et al.,<br />

1992). Results obtained in the present study demonstrate<br />

that large seeds could allow seedling to survive for longer<br />

days after emergence. On the other hand, small size offer<br />

short period of persistence from emergence, which is in<br />

agreement with the results obtained by Westoby et al.<br />

(1992). The present study also indicates that it is not likely<br />

to relate the seed size to the seed mass. In other words,<br />

large seeds are not always heavy and small seeds are not<br />

necessarily light (e.g. Rununculus and Carduus).<br />

Results of several comprehensive studies (e.g. Schimpf,<br />

1977; Sorenson & Miles, 1978; Stronberg & Patten, 1990)<br />

have suggested that plants in xeric habitats tend to have<br />

larger seeds, and consequently larger seeds might provide<br />

an advantage for seedling establishing in dry conditions.<br />

However, this study showed that xeric habitats tend to<br />

have smaller seeds. The advantage of large seeds in the<br />

arid and semi-arid habitats may be due to the fact that<br />

large seeds disperse over smaller distance and may attract<br />

herbivores (Westoby & Leishman, 1994). A seed may be<br />

large because it encloses an embryo (and endosperm)<br />

which have genotypes that are able to attract a greater<br />

than average supply of nutrient resources (Mogie et al.,<br />

1990). However, the number of seeds and their size in<br />

the present study seem to be largely determined by the<br />

ecology of the species.<br />

It is evident that very few species could tolerate more<br />

than 2% of NaCl solution (Chapman, 1966). This con-<br />

ecologia mediterranea, tome 29, fascicule 2, 2003

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