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биота российских вод японского моря - Materials of Alexey Shipunov

биота российских вод японского моря - Materials of Alexey Shipunov

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far as the Tatar Strait (Bokhan, 1984). The species is also transported by the warmKuroshio Current to the north-eastern tip <strong>of</strong> Hokkaido Island and to the South KurilIslands (Onbe et al., 1996).Biology and ecology. P. tergestina is a warm-water species <strong>of</strong> the Peter theGreat Bay fauna, appearing in the middle <strong>of</strong> summer hydrological season. In 1973 itappeared in Alekseev Bight in August at a temperature <strong>of</strong> 21.1°C and in September (at17.9°C) reached maximum density (59 sp./m 3 ). As water got colder, the density <strong>of</strong> thespecies sharply decreased, but it still occurred sporadically until December (Mikulich& Biryulina, 1977).In the south-western part <strong>of</strong> Peter the Great Bay small numbers <strong>of</strong> P. tergestinaappear in late August, its density growing in September up to 141 sp./m 3 (Shkoldina &Shevchenko, 2001). In September <strong>of</strong> 1996 gamogenetic females with one-two developingresting eggs each were recorded in some regions <strong>of</strong> the bay at a surface watertemperature <strong>of</strong> 17–19°C.In Vostok Bay P. tergestina usually appears in mid-August when the water iswarmest (22.4°C), reaching a density <strong>of</strong> 186 sp./m 3 , which decreases to 3.3 sp./m 3 inSeptember (Shkoldina, 2001). It occurs singly until late October, when water temperatureis 13–14°C. At this period gamogenetic females with resting eggs are found, too.The species’ biology and ecology was intensively studied for the Inland Sea <strong>of</strong>Japan. Onbe’s records (1974) show that this species appears among the plankton inlatitude about 34°20′N in May or June, reaching maximum abundance in July-Augustand staying in the sea until September-October. Maximum density (8.7–9.4 thousandsp./m 3 ) is registered at a temperature <strong>of</strong> 22.3–23°C, but in September assemblages upto 30 thousand sp./m 3 were recorded. The bulk <strong>of</strong> the cladocerans inhabit the upperlayer <strong>of</strong> water (10–15 m), concentrating at a depth <strong>of</strong> 3 m in July and nearer to the surfacein August. At night the number <strong>of</strong> females with mature embryos is maximal, andbefore dawn the young hatch. The same patterns <strong>of</strong> reproduction were observed in theCaspian Evadne (Rivier, 1969). During a period <strong>of</strong> gamogenetic reproduction a populationincludes from 2.2 to 12.5% <strong>of</strong> males and up to 12.4% <strong>of</strong> females with restingeggs. Females with resting eggs are among the largest specimens in a population(Onbe, 1978b). Japanese scientists observed the hatching <strong>of</strong> a young P. tergestinafrom a resting egg (pl. VIII, fig. 1). The process begins, like in all the Polyphemoidea,when a rounded egg breaks up into 2 unequal halves; an embryo at this stage alreadyhas a well-pigmented eye. The size <strong>of</strong> a resting egg varies from 190 to 240 µm (averagesize is 200 µm). Resting eggs are found in sediments all the year round, theirnumber is maximal (7.7 thousand eggs/m 2 ) in July, with the peak density <strong>of</strong> the cladoceransin the plankton about 3 thousand sp./m 3 (Onbe, 1985).Among the contents <strong>of</strong> the foregut <strong>of</strong> P. tergestina large centric diatoms werefound (Kim et al., 1989).3. Genus Podon Lilljeborg, 1853Type species: Podon leuckarti (Sars, 1862).Shell in females rounded, in males small, having irregular shape. Head elongated,anteriorly globular, separated from shell by clearly seen depression. Antennalbranches with well-developed apical segments; number <strong>of</strong> setae on 4-segmented and3-segmented branches identical (6 setae). Exopods <strong>of</strong> thoracic limbs weakly devel-19

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