Revue internationale d'écologie méditerranéenne International ...
Revue internationale d'écologie méditerranéenne International ...
Revue internationale d'écologie méditerranéenne International ...
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Removal of lemma improved germination at<br />
low water potentials, and this beneficial effect<br />
of lemma removal remained after dry storage<br />
(Table 5, to be compared with Figure 5).<br />
Discussion and Conclusions<br />
Mature dispersal units of the two cytotypes of<br />
Lygeum spartum (polyploid one with 2n = 40<br />
and diploid one with 2n = 16), collected in<br />
Algeria in June were considered as dormant<br />
(Figures 1 and 2). They germinated poorly in<br />
darkness (Figure 1), and their germination<br />
was very slow (Table 2). The thermal optimum<br />
for germination (20-25 o C) was similar<br />
to that found for numerous species from hot<br />
semideserts and deserts (Baskin & Baskin<br />
1998), such as Stipa sp. (Lodge & Whalley<br />
1981; Fulbright et al. 1983; White & Van<br />
Auken 1996) and Aristida sp. (Mott 1974).<br />
Continuous white light inhibited germination<br />
of freshly harvested L. spartum dispersal units<br />
(Figure 4), suggesting that germination in nat-<br />
ecologia mediterranea – Vol. 36 (1) – 2010<br />
Environmental control of germination and dormancy of seeds of two cytotypes of Lygeum spartum L.,<br />
a perennial grass of semi-arid and arid areas in Algeria<br />
Table 4 – Germination percentages obtained after 14 days at 25 o C,<br />
in darkness and in continuous white light, with freshly harvested<br />
and after-ripened isolated caryopses collected in arid highlands<br />
and semi-arid littoral coast. Means of the results obtained<br />
in 2 replicates of 25 seeds ± arithmetical spread.<br />
ural conditions is considerably restricted<br />
when seeds are exposed to direct sunlight.<br />
Such a negative photoblasty has been reported<br />
for numerous xeric grasses such as Bromus<br />
rubens, B. scoparius and B. rigidus (Corbineau<br />
et al. 1992; Kigel 1995), Hordeum<br />
spontaneum (Gutterman et al. 1996), Panicum<br />
turgidum (Koller and Roth 1963), Stipa bromoides,<br />
S. lagascae, Aristida caerulescens<br />
and Aegilops longissima (Kigel 1995), and in<br />
other species including Schismus arabicus<br />
Germination (%) obtained in<br />
Cytotype (Origin) Caryopses darkness light<br />
Diploid freshly harvested 90 ± 6 68 ± 8<br />
(Arid highlands) after-ripened 90 ± 4 92 ± 2<br />
Polyploid freshly harvested 80 ± 4 52 ± 4<br />
(Semi-arid littoral coast) after-ripened 92 ± 2 72 ± 4<br />
Table 5 – Germination percentages obtained after 14 days at 25 o C, in darkness, in water (0 MPa) and in PEG solutions at –0.2, –0.5,<br />
1.0 and –1.5 MPa with freshly harvested and after-ripened isolated caryopses collected in arid highlands and semi-arid<br />
littoral coast. Means of the germination percentages obtained in 2 replicates of 25 seeds ± arithmetical spread.<br />
Germination (%) after 14 days in<br />
water PEG solutions at (MPa)<br />
Cytotype (Origin) Caryopses (0 MPa) – 0.2 – 0.5 – 1.0 – 1.5<br />
Diploid freshly harvested 90 ± 6 82 ± 6 66 ± 4 32 ± 6 6 ± 2<br />
(Arid highlands) after-ripened 90 ± 9 96 ± 2 88 ± 6 76 ± 6 6 ± 2<br />
Polyploid freshly harvested 92 ± 2 66 ± 4 42 ± 6 18 ± 4 0<br />
(Semi-arid littoral coast) after-ripened 80 ± 4 90 ± 6 70 ± 6 30 ± 6 0<br />
Figure 5 – Effects of<br />
water potential of<br />
the medium on the<br />
germination<br />
percentages<br />
obtained after<br />
14 days in darkness<br />
with freshly<br />
harvested () and<br />
after-ripened ()<br />
dispersal units of<br />
the diploid cytotype<br />
collected in arid<br />
highlands (A) and of<br />
the polyploid<br />
cytotype collected in<br />
semi-arid littoral<br />
coast (B). Means of<br />
the results obtained<br />
in 2 replicates of 25<br />
seeds ± arithmetical<br />
spread.<br />
95