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anglicky - Institute of Hydrobiology

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mothers clearly come from the autumnal population, the neonates born immediately after the<br />

isolation <strong>of</strong> the mothers (here referred to as 1 st <strong>of</strong>fspring) had passed their oogenesis and<br />

embryogenesis at low temperatures in the reservoir, the 2 nd <strong>of</strong>fspring passed their oogenesis in<br />

the reservoir and their embryogenesis in the experiment, the 3 rd <strong>of</strong>fspring passed both <strong>of</strong> these<br />

ontogenetic phases in the experiment. The results reveal that low temperature was the main<br />

factor causing low FSN in neonates.<br />

5 ºC<br />

20 ºC<br />

FSN<br />

70<br />

60<br />

50<br />

70<br />

60<br />

50<br />

lake water with natural<br />

seston<br />

GF/C filtered lake<br />

water - high food<br />

GF/C filtered lake<br />

water - low food<br />

40<br />

mothers<br />

1st<br />

<strong>of</strong>fspring<br />

2nd<br />

<strong>of</strong>fspring<br />

3rd<br />

<strong>of</strong>fspring<br />

40<br />

mothers<br />

1st<br />

<strong>of</strong>fspring<br />

2nd<br />

<strong>of</strong>fspring<br />

3rd<br />

<strong>of</strong>fspring<br />

Fig. 6: Filtering setae number (FSN) <strong>of</strong> D. galeata mothers and that <strong>of</strong> their <strong>of</strong>fspring in three<br />

consecutive clutches. The mothers were isolated from Římov Reservoir on January 29 and<br />

kept in the laboratory at two temperatures and three feeding treatments (amount <strong>of</strong> the<br />

natural seston – 0.2 mg l –1 POC, high food and low food treatments – 2 and 0.2 mg l –1 POC<br />

<strong>of</strong> Scenedesmus subspicatus culture, respectively).<br />

The succession <strong>of</strong> ontogenetic phases and different temperature treatments during the<br />

experiment suggested that the time in which low temperature may induce lower FSN is very<br />

probably the period <strong>of</strong> embryonic development (embryogenesis). This was tested in another<br />

experiment, in which eggs obtained from a laboratory clone <strong>of</strong> D. galeata were incubated in<br />

vitro at three different levels <strong>of</strong> temperature. The eggs were removed several hours after being<br />

deposited in the brood pouch <strong>of</strong> the female and divided into three groups. Each group <strong>of</strong> the<br />

Table 6: Results <strong>of</strong> in vitro embryogenesis in D. galeata eggs incubated at three different<br />

temperatures (figures with different superscripts are significantly different, unequal n HSD<br />

tests, p=0.05).<br />

Temperature during embryogenesis 19°C 10°C 6°C<br />

Carapace length in the1st instar <strong>of</strong>fspring<br />

(µm ± 95% C.I.) 502 (±7) a 454 (±11) b 446 (±14) b<br />

FSN in <strong>of</strong>fspring<br />

(± 95% C.I.) 72 (±1) a 69 (±1) a 65 (±1) b<br />

same clutch was then incubated at a different temperature (19, 10, and 6°C). FSN was found<br />

to be significantly lower in individuals incubated during embryogenesis at the lower<br />

temperatures (Table 6). The difference in FSN is partly attributable to a difference in the<br />

body size <strong>of</strong> the neonates because the neonates from the lower temperatures were significantly<br />

smaller and a direct relationship between neonate size and FSN in their filtering screens was<br />

32

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