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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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1. Thysanoessa inermis (Kroyer, 1846)(Pl. I, fig. 1; II, fig. 1)Kroyer, 1846: pl. 7, figs. 2,3 (Thysanopoda inermis, T. neglecta); G.O. Sars, 1883: 51–52(Euphausia inermis, Thysanoessa borealis); Hansen, 1911: 8; Lomakina, 1978: 183–185, figs.112, 113; Baker et al., 1990: p. 74, fig. 9b (Thysanoessa inermis).Description. Frontal plate <strong>of</strong> rostrum long, reaching end <strong>of</strong> first segment <strong>of</strong> antennularpeduncle, lanceolate, with pointed tip. Eyes without (forma inermis) or withconstriction; upper lobe narrower (f. neglecta). Carapace without lateral spine. Thoracopodsidentical in arrangement (f. inermis), or thoracopods 2 modified into graspingorgans (f. neglecta) due to elongated segments 4 and 5 and inflated basal segments.Distal 6th abdominal segment shorter than 2 penultimate segments (4 and 5) takentogether; its posterior end with small mid-dorsal spine pointed backward. Fifth abdominalsegment <strong>of</strong>ten with similar spine.Length <strong>of</strong> body in euphausiids from northern part <strong>of</strong> Sea <strong>of</strong> Japan up to 34 mm.Remarks. The studies <strong>of</strong> the North Atlantic euphausiid fauna showed that formaneglecta is a stage <strong>of</strong> T. inermis, represented by late larval stages and juveniles. Adultspecimens <strong>of</strong> f. neglecta are very rare and have not been recorded in the Northern Pacific,particularly in the Sea <strong>of</strong> Japan (Lomakina, 1978).Nemoto (1966) discovered a phenomenon <strong>of</strong> wedgewise change <strong>of</strong> the rate <strong>of</strong>specimens with spines at the end <strong>of</strong> fifth and sixth abdominal segments. The percentage<strong>of</strong> specimens with two spines decreases westward, from 75% in Alaska Bay to16% in the Sea <strong>of</strong> Okhotsk. He also reports single finds <strong>of</strong> specimens with spines onabdominal segments 6, 5, and 4.Distribution. T. inermis is a widespread boreal-arctic species. In the northwesternpart <strong>of</strong> the Pacific Ocean it has not been recorded south <strong>of</strong> 37˚ N in the Sea <strong>of</strong> Japanand the Pacific side <strong>of</strong> the South Kuril Islands. In the northeastern part <strong>of</strong> the PacificOcean the species has not been recorded south <strong>of</strong> 52˚ N. In the Atlantic Ocean itis found north <strong>of</strong> 39˚ N near the American coasts, in the La Manche and Skagerrakstraits. In the Arctic T. inermis is possibly circumpolar, found in all seas <strong>of</strong> Russia, inthe Beaufort Sea, in the east <strong>of</strong> the Canadian part <strong>of</strong> the Arctic, and around Greenland.In the Sea <strong>of</strong> Japan the southern boundary <strong>of</strong> the distributional range <strong>of</strong> this specieslies north <strong>of</strong> 37˚ N near the continent and 39˚ N near the Japan coast. In the TatarStrait it occurs to 51˚ N. The densest swarms <strong>of</strong> this species were observed in the easternhalf <strong>of</strong> the sea near the northern Hokkaido and the South Sakhalin in spring.Habitat and breeding. T. inermis is an epi- to mesopelagic species, in the Sea <strong>of</strong>Japan found to depths around 1000 m (Vinogradov, 1968). Spring pre-breeding andbreeding assemblages begin to accumulate near the northern Hokkaido in the secondhalf <strong>of</strong> March, with maximum concentration in the near-surface layer. Then assemblagesmove northward, to the coastal zone <strong>of</strong> the southwestern Sakhalin up toIliynsky shoal (about 48˚ N). Phenological wave passes over the eastern part <strong>of</strong> the seanorthward from Hokkaido to 50˚ N from March to late May-early June. In Peter theGreat Bay mass breeding <strong>of</strong> T. inermis begins in the second to third decade <strong>of</strong> April.Diameter <strong>of</strong> egg capsules 600–925 µm, perivitelline space well developed (80–86% <strong>of</strong>the whole egg volume).Euphausiids <strong>of</strong> this species feed on meso- and microzooplankton, phytoplankton,and if food is scarce, on detritus and other euphausiids.84

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