Evadne nordmanni Loven, 1836(Pl. VII, figs. 1–10)Loven, 1836: 1, tabl. 1–2, figs. 1–16; Müller, 1867: 222, tabl. 6, figs. 8–10; Lilljeborg,1900: 647, tabl. 86, figs. 4–17; Rammner, 1930: 5, figs. 9, 10; Dolgopolskaya, 1958: 46–50,figs. 14–16; Manuilova, 1964: 307–308, fig. 176; Cheng & Chen, 1966: 174, pl. 2; Yamazi,1966: 192–193, pl. 88, fig. 5; Mordukhai-Boltovskoi, 1969: 23, pl. III, fig. 4; Flössner, 1972:398–400, abb. 187; Onbe, 1974: 90–92, fig. 6, A; Negrea, 1983: 351–355, fig. 146; Mordukhai-Boltovskoi& Rivier, 1987: 123–125, fig. 78; Rivier, 1998: 135–136, figs. 101–109(Evadne nordmanni).Description. Parthenogenetic female. Shell elongated, with pointed apex, inold specimens with many embryos, oval, with rounded outline. Swimming antennaesmall, with decreased apical segments. Head not separated from shell. Exopod <strong>of</strong> limb1 almost equal in length to second segment <strong>of</strong> endopod; exopods <strong>of</strong> limbs 2–3 small.Each exopod <strong>of</strong> limbs 1–2 with two setae, each exopod <strong>of</strong> limbs 3 with one seta; setalformula 2.2.1.1. Maxillary process well developed on limbs 2 and 3. Apical setae onendopod <strong>of</strong> limb 1 long, on endopod <strong>of</strong> limbs 2 and 3 short and claw-like. Cauda inshape <strong>of</strong> 2 conical pointed outgrowths. Length 0.6–0.7 mm, height up to 1.2–1.4 mm.Gamogenetic female generally has one resting egg. Females with restingeggs almost largest specimens in population.Male. Shell almost triangular. Testes protruded into shell cavity, clearly visible.Hooks on limb 1 thin, not pointed. Length 0.5–0.65 mm, height 0.7–0.8 mm.Distribution. E. nordmanni is distributed in cold and temperate waters. It occursin the open seas <strong>of</strong> the Arctic, Pacific, and the Atlantic oceans (excluding the tropicalzones <strong>of</strong> the Pacific and the Atlantic); in the inland seas, namely the White, Baltic,Mediterranean, Black seas, and the Inland Sea <strong>of</strong> Japan (Rivier, 1998); as well as inthe Far East seas (Kun, 1975).In the north-western Pacific, the northernmost record <strong>of</strong> E. nordmanni is from thesouth <strong>of</strong> the Bering Sea, near Africa Cape (Vinogradov, 1956), whereas Podon leuckartiis distributed farther north. In the western part <strong>of</strong> the Bering Sea E. nordmannioccurs in the plankton at the beginning <strong>of</strong> autumn (September and October), when thewater is warmest (Geinrich, 1961). In the Sea <strong>of</strong> Okhotsk the species can breed in thecoastal zone around the whole periphery <strong>of</strong> the sea (Lubny-Gertsyk, 1959). Near thesouthern tip <strong>of</strong> Sakhalin Island E. nordmanni inhabits Aniva Bay and penetrates intothe Sea <strong>of</strong> Japan via the La Perouse Strait (Ponomareva, 1961). It is a common speciesfor the north-western part <strong>of</strong> the Sea <strong>of</strong> Japan, occurring in all bights and bays, includingPeter the Great Bay (Kos, 1960; Shkoldina, 2001, 2002).Cold currents bring E. nordmanni to the southern part <strong>of</strong> the Sea <strong>of</strong> Japan, alongthe coast <strong>of</strong> Korea. The farther south, the earlier (mid-spring to early spring) E. nordmanniappears in the plankton (Kim, 1985; Yoo & Kim, 1987; Onbe et al., 1996). Thespecies also occurs near China (Jian Dong, 1991).Biology and ecology. E. nordmanni is a temperate-cold water species. Its rangeis extended in north-south direction, and the periods <strong>of</strong> occurrence <strong>of</strong> this species inthe plankton depend on the latitude and are regulated by the same mechanisms as inPodon leuckarti. In the Sea <strong>of</strong> Okhotsk and the Bering Sea E. nordmanni appears inlate summer or in autumn (Vinogradov, 1956). In the Tatar Strait (49°–51°30′N) theappearance <strong>of</strong> all the podonid species depends on the extent <strong>of</strong> the warming up <strong>of</strong> the23
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
- Page 3 and 4: BIOTA OF THE RUSSIAN WATERS OF THE
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- Page 28 and 29: Mordukhai-Boltovskoi, F.D. 1968. On
- Page 30 and 31: Plate I. Penilia avirostris (1-4 -
- Page 32 and 33: Plate III. Pleopis polyphemoides: 1
- Page 34 and 35: Plate V. Podon leuckarti: 1 - parth
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- Page 38 and 39: CLASS MALACOSTRACA Latreille, 1802O
- Page 40 and 41: way) to Greenland, the Spitsbergen,
- Page 42 and 43: Plate II. Nebalia bipes: 1 - distal
- Page 44 and 45: The mysids inhabit marine, brackish
- Page 46 and 47: 1. Genus Archaeomysis Czerniavsky,
- Page 48 and 49: 1. Genus Holmesiella Ortmann, 1908T
- Page 50 and 51: Distribution. M. microphthalma is a
- Page 52 and 53: as all female pleopods, rudimentary
- Page 54: Description. Antennal scale 4.3-9.4
- Page 57 and 58: 2. Neomysis awatschensis (Brandt, 1
- Page 59 and 60: 6. Genus Boreoacanthomysis Fukuoka
- Page 61 and 62: 8. Genus Exacanthomysis Holmquist,
- Page 63 and 64: exopod with one simple lateral seta
- Page 65 and 66: Mauchline, J. 1980. The biology of
- Page 67 and 68: Plate II. Archaeomysis grebnitzkii
- Page 69 and 70: Plate IV. Meterythrops robusta (1-4
- Page 71 and 72: Plate VI. Xenacanthomysis pseudomac
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Plate X. Neomysis awatschensis: 1 -
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Plate XII. Neomysis mirabilis: 1 -
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Plate XIV. Exacanthomysis stelleri:
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Plate XVI. Paracanthomysis shikhota
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(pl. III, figs. 2, 7-9), do not fee
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1. Thysanoessa inermis (Kroyer, 184
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35°45′N) of Honshu Island. In th
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Hansen, H.J. 1911. The genera and s
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Plate II. Dorsal view of anterior p
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SUBPHYLUM CHELICERATA HEYMONS, 1901
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The class Pycnogonida is currently
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14(15). Compound spines with 1 pair
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Geographical distribution. N. brevi
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*Nymphon longitarse brevicollis Los
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6. Nymphon hodgsoni Schimkewitsch,
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8. Nymphon uniunguiculatum Losina-L
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2 segments; adults have vestigial c
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2. Achelia bituberculata Hedgpeth,
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setae. Oviger relatively short; ovi
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Description. Utinomi’s collection
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Geographical distribution. A. echin
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1. Lecythorhynchus marginatus Cole,
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ears 4 large spines on sole proxima
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2(1). Lateral processes and coxae 1
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*Genus Callipallene Flinn, 1929Type
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*Genus Phoxichilidium Milne-Edwards
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eyond proboscis; chelas much shorte
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KEY TO THE SPECIES OF THE GENUS COL
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Abdomen cylindrical, pointed horizo
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Kim, I.H. & J.S. Hong. 1986. Korean
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Turpaeva, E.P. 2004b. Shallow-water
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Plate II. Nymphon grossipes (from S
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Plate IV. Nymphon longitarse longit
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Plate VI. Nymphon japonicum (from N
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Plate VIII. Nymphon stocki (from Ut
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Plate X. Achelia kurilensis (from L
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Plate XII. Achelia gracilipes (from
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Plate XIV. Tanystylum scrutator (fr
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Plate XVI. Nymphonella tapetis (fro
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Plate XVIII. Decachela discata (fro
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Plate XX. Phoxichilidium ungellatum
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Plate XXII. Anoplodactylus pygmaeus
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INDEX OF LATIN NAMES *AAcanthomysis
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Oochoticum, brevirostre Nymphon 98o