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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

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