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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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water from year to year. For example, in cold years (1975) only E. nordmanni and Podonleuckarti were found in this area (Bokhan, 1984).In the southernmost part <strong>of</strong> the Russian Far East waters (Peter the Great Bay) E.nordmanni appears in spring and reaches maximum density in early summer and inautumn. Thus, in Amursky Bay (Alekseev Bight <strong>of</strong> Popov Island) the species occurredin the plankton May through January and had two peaks <strong>of</strong> density, from mid-June tomid-July and from mid-October to mid-November. First specimens were recorded inMay at a water temperature <strong>of</strong> 5°C, in June at an average temperature <strong>of</strong> 13.2°C thedensity was 230 sp./m 3 , and in autumn, when temperature ranged from 9 to 3°C, apopulation maximum <strong>of</strong> 162 sp./m 3 was recorded (Mikulich & Biryulina, 1977).Chuchukalo et al. (1980) show that E. nordmanni appeared in Amursky Bay(near Reineke Island) in early June at a water temperature <strong>of</strong> 11–13°C, and in July (at21°C) the density already attained 7 thousand sp./m 3 . Temperature rising to 21–22.3°CJuly through late August, E. nordmanni decreased in numbers to 0.5 thousand sp./m 3 .In late autumn (November) at a temperature <strong>of</strong> 7.1°C the abundance <strong>of</strong> the speciesslightly enhanced (Chuchukalo et al., 1980).In the south-western part <strong>of</strong> Peter the Great Bay E. nordmanni is vertically distributedfrom 0 to 50 m. Its peak density was recorded for July (in Kalevala Bight, 3.5thousand sp./m 3 ); in August, when temperature was the warmest (21°C), the densitysharply decreased; and in September rose again (Shkoldina & Shevchenko, 2001).Kos’ records (1976) display that in mid-summer (late June–early July) the density <strong>of</strong>E. nordmanni was low (5–25 sp./m 3 ) in Possjet Bay at a temperature <strong>of</strong> 17–20°C. Inthis bay the species was found at a temperature <strong>of</strong> 6.6–21°C and a salinity <strong>of</strong> 26.31–33.17‰. A maximum density <strong>of</strong> E. nordmanni (260 sp./m 3 ) was registered at <strong>of</strong>fshorestations (Kos, 1977).In the south-western part <strong>of</strong> Peter the Great Bay gamogenetic females with latenteggs were recorded for July and September, and were not found in August. It may indicatethat E. nordmanni has two reproduction cycles in the southern part <strong>of</strong> its distributionalrange. In 2002 in Vostok Bay E. nordmanni occurred in the plankton untillate October, at a temperature <strong>of</strong> 12–13°C, and females with well-developed restingeggs constituted the bulk <strong>of</strong> the population.The biology and ecology <strong>of</strong> E. nordmanni are most extensively studied for the InlandSea <strong>of</strong> Japan (34°N). In this area the species appears in March-April and disappearsin June; it attains a maximum density <strong>of</strong> 2.7–3.4 thousand sp./m 3 at 15–16°C. E.nordmanni appears in the plankton at a temperature from 8 to 11°C and disappears at atemperature from 21.4 to 23.8°C (Onbe, 1974). In March and April females have thelargest size (length up to 0.55–0.6 mm) and highest fecundity (up to 10–12 embryos).Males and gamogenetic females appear in the population in mid-June, and by the end<strong>of</strong> the month parthenogenetic females almost disappear (Onbe, 1974). Resting eggsare light brown and have a size <strong>of</strong> about 200 µm (Onbe, 1985).The analysis <strong>of</strong> the intestine’s content showed that E. nordmanni feeds on largecentric diatoms, particularly Skeletonema costatum. On other evidence, the podonidsmay also consume din<strong>of</strong>lagellates (Kim et al., 1989).24

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