Revue internationale d'écologie méditerranéenne International ...
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ecologia mediterranea, tome 29, fascicule 2, 2003, p. 153-164<br />
INTERPRETING GERMINATION RESULTS BASED ON SEED SIZE, MASS AND ECOLOGICAL… ◆<br />
firmed by Zahran (1975) in his studies on Juncus rigidus<br />
seeds that succeeded to germinate at salinity level of 3%<br />
NaCl solution. Accordingly, he reported that the success<br />
or failure of seed germination in saline soil might be an<br />
indicator for the success or failure of seed propagation of<br />
salt tolerant plant in saline soil.<br />
Annuals in desert ecosystems exploit top centimeters<br />
of the soil, and are abundant only when surface moisture<br />
is relatively high. Moisture conditions of the surface<br />
soil vary less spatially than they do temporally (Olsvig-<br />
Whittaker et al., 1983). Hence, spatial heterogeneity of<br />
annuals as a response to local environmental variation<br />
may be relatively low, although countered by biologically<br />
caused patterning. Baker (1972) compared seed weight<br />
of the California flora with moisture availability of each<br />
habitat. He reported that among herbaceous species there<br />
was a significant negative correlation between moisture<br />
availability and seed weight. Westoby et al. (1992) argued<br />
that Baker’s data should be regarded cautiously. However,<br />
in the present study, there was a highly significant correlation<br />
between seed weight, seed size of annuals and the<br />
moisture availability of the natural habitats they collected<br />
from as well as the water supply allowed in the laboratory<br />
experiments. This trend is disagreeing with Baker<br />
(1972). On the other hand, Mazer (1989) working on<br />
Indian Dunes flora reported no significant association<br />
between seed mass and moisture availability. This trend<br />
is also noted in this study where there is no significant<br />
correlation between moisture level and seed mass of the<br />
species collected from xeric and dried habitats, such as<br />
the inland plateau, saline depressions, sand dunes and<br />
rocky cliffs habitats (see values of correlation in table 1).<br />
Similarly, Telenius and Torstensson (1991) did not find<br />
any association between seed weight and moisture availability<br />
in 48 species from the genus Spergularia. However,<br />
the comparative evidence for an association between large<br />
seed mass and dry habitats is quite limited, despite its<br />
general acceptance in the literature. On the other hand,<br />
Guerrero-Campo and Fitter (2001) reported that plant<br />
species with shallow or thin main root had smaller seeds<br />
than plants with fibrous or other adventitious roots. They<br />
concluded that seed size was related to plant height, but<br />
this association was weaker than that between seed size<br />
and root depth. Their results suggested that traditional<br />
ecological explanation do not explain the relation between<br />
seed and adult plant size, and they proposed that deeprooted<br />
plants have large seeds because of allometric and<br />
developmental constraints, which means that only large<br />
seeds can produce the thick roots that can grow rapidly<br />
to depth. The abundant literature that demonstrates the<br />
adaptation of plants to the conditions prevailing in their<br />
habitats showed that natural selection operates, at a very<br />
fine level, genotypes that are most efficient at gathering<br />
the resources of the local habitats (Heslop-Harrison,<br />
1964). The changes in moisture and salinity in different<br />
habitats are reflected in the changes of the produced<br />
progeny (seeds). It seems that with the greater austerity<br />
in available moisture resources most of the plant species<br />
directed to produce small seeds. As stated above larger<br />
seed size is not necessarily associated with larger mass.<br />
It is unlikely that the advantage of large seeds was due to<br />
the ability to emerge from greater depth in the soil, where<br />
soil moisture is more favorable. Experimentation on the<br />
behavior of the studied species should be the next step<br />
in clarifying the mode of that behavior and its relevant<br />
to the habitats.<br />
ACKNOWLEDGMENTS<br />
The author sincerely wishes to thank Dr. Nabil El-<br />
Hadidi, Professor of plant taxonomy and flora & the keeper<br />
of Cairo University Herbarium for the identification<br />
of the plant specimens. The author also acknowledges<br />
the valuable comments of Dr. M. Abdel-Razik & Dr. S.<br />
El-Darier, Professors of plant ecology and Dr. S.Y.<br />
Barakat, emeritus Professor of plant physiology, Faculty<br />
of Science Alexandria University. I wish to thank my<br />
colleague Dr. H. Deif for his kind help in preparing the<br />
photographs.<br />
References<br />
ALLEN S., GRIMSHAW H. M., PARKINSON J. A. & QUARMBY C.,<br />
1974. Chemical analysis of ecological materials: Blackwell<br />
Scientific Publications, Oxford and London. 565 p.<br />
Baker H.G., 1972. Seed weight in relation to environmental<br />
conditions in California. Ecology, 53: 997-1010.<br />
Baskin J.M. & Baskin C.C., 1992. Seed germination biology<br />
of the weedy biennial Alliaria pelidata. Nat. Areas J., 12:<br />
191-197.<br />
Bl at e G.M., Pear t D.R. & Leight on M., 1998. Post-dispersal<br />
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Boul os L., 1995. Flora of Egypt: Checklist. Al-Hadra Publishing,<br />
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Chapin F.S. III., 1980. The mineral nutrition of wild plants.<br />
Annu. Rev. Ecol. Syst., 11: 233-260.<br />
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