SUBPHYLUM CRUSTACEACLASS BRANCHIOPODA Latreille, 1817Superorder CLADOCERAMilne-Edwards, 1840 sensu Negrea et al., 1999Irina K. Rivier 1 , Larissa S. Shkoldina 2General characteristics 3Cladocerans (superorder Cladocera) is a peculiar group <strong>of</strong> very small (usuallysmaller than 1 mm, rarer up to 4 mm) planktonic crustaceans <strong>of</strong> freshwater origin.They inhabit various continental and marine waters, where they are abundant and <strong>of</strong>tendominate.The body <strong>of</strong> most cladocerans is enclosed in a thin transparent shell, the dorsalpart <strong>of</strong> which (brood pouch) bears embryos, while the lateral parts (valves) protectthoracic limbs in filter-feeding cladocerans; in predatory cladocerans the valves arenot developed. Marine forms (Penilia and Podonidae) have the enclosed brood pouchcovered by shell, which isolates embryos from the external environment. In the Podonidaethe shell containing the brood pouch is enlarged; it grows together with embryosand has a hydrostatic function as well.The body <strong>of</strong> cladocerans is divided into a head, a thorax, a usually reduced abdomen,and a postabdomen (cauda). There is a compound eye and an ocellus (“naupliuseye”), which is reduced in some taxa. The first pair <strong>of</strong> antennae (antennules)represents sense organs provided with papillae (aestetascs) and short sensory setae,obviously performing a tactile function. In males the antennules are usually movableand longer than in females. Antennae 2 are locomotory organs. The mouth parts(mandibles, maxillulae and maxillae) are situated posteriorly. They are used to manipulateand push food particles into the gut. The body is indistinctly segmented andprovided with four to six pairs <strong>of</strong> thoracic limbs, being filtering organs in most cladoceransand grasping organs in predators. The postabdomen is situated posteriorly andusually provided with claws and “swimming” setae (setae natatoriae).The distinctive feature <strong>of</strong> the cladocerans’ life cycle is direct development (excludingthe genus Leptodora, which has the stage <strong>of</strong> a metanauplius larva; the Leptodoridaeare presently separated in the superorder Leptodorida) and the alternation <strong>of</strong>gamogenetic and parthenogenetic reproduction, including the stage <strong>of</strong> a resting (latent)egg. Hatching newborn cladocerans (the first generation) from resting eggs give rise toseveral parthenogenetic generations. In most cladocerans parthenogenetic eggs devel-1 I.K. Rivier is the author <strong>of</strong> the systematic part <strong>of</strong> the chapter “Podonidae” and <strong>of</strong> the figures<strong>of</strong> Podonidae (excluding figs. 1–3, 5 in pl. VIII).2 L.S. Shkoldina is the author <strong>of</strong> the chapter “Sididae” and figures 1–4 in plate I (Penilia avirostris).3 The chapter “General description” and the parts concerning distribution, biology, and ecologyare written by the authors in collaboration.9
oping in the brood pouch have a full reserve <strong>of</strong> nutrients for embryos. But in members<strong>of</strong> the genus Penilia and the Onychopoda (Polyphemoidea) parthenogenetic eggs donot have the same reserve and get nutrients from the inner hypodermic wall <strong>of</strong> thebrood pouch. Eggs develop in the brood pouch into tiny young cladocerans, whichhatch out and grow into adults, going through several ecdyses. The young <strong>of</strong> the Polyphemoidaehatch out by the destruction <strong>of</strong> female’s brood pouch; these young are bornsexually mature.The appearance <strong>of</strong> males in populations depends on unfavourable conditions. Afterfertilization the ovicell begins to accumulate yolk in the ovary. After the period <strong>of</strong>trophoplasmatic growth in the ovary, resting eggs having only an elastic membraneflow to the brood pouch where dense chitinous membranes are formed. In the podonidsat complete ripening <strong>of</strong> the eggs the death <strong>of</strong> a female follows, and the restingeggs sink to the bottom (Swammerdam, 1685). Unlike the Cercopagidae, amongwhich particular gamogenetic females appear, in the Podonidae the resting eggs aredeveloped in parthenogenetic females after fertilization. The resting egg, covered withthick chitinous membranes protecting it from unfavourable environment conditions,rests on oozy sediments.The present work is based on the taxonomic system, by which the superorderCladocera includes three orders: Ctenopoda (two families), Anomopoda (ten families),and Onychopoda (three families) (Dumont & Negrea, 2002). The superorder Cladoceracontains more than 450 species belonging to 52 genera. Most cladocerans (95%) arefound in freshwater habitats, 3% (about 30 species) – in brackish water habitats (includinglandlocked seas, e.g. the Caspian and the Aral), and only eight species occurin marine environments (Bowman & Abele, 1982). One <strong>of</strong> these species belongs to thefamily Sididae (Penilia avirostris Dana, 1849), and other seven to the family Podonidae.All eight species occur in the Sea <strong>of</strong> Japan, and seven <strong>of</strong> them, excluding Podonintermedius Lilljeborg, 1853, are found in its northwestern part (Peter the Great Bay).Most cladocerans, including Sididae, are filter feeders; they feed on algae, bacteria,and detritus. Species <strong>of</strong> the order Onychopoda (Polyphemoidea) are mostly predators,feeding on larger organisms (small crustaceans, rotifers, protozoans, and algae).Cladocerans represent the important trophic part <strong>of</strong> plankton communities, being consumers<strong>of</strong> organic matter and food for other organisms, particularly for fishes.Cladocerans are typical neritic species <strong>of</strong> the Sea <strong>of</strong> Japan. The coastal zone inhabitedby various neritic animals is 3–5 miles wide in the northern part <strong>of</strong> the Sea <strong>of</strong>Japan, narrowing southward to a width <strong>of</strong> 0.5–1 mile within the Korea Strait and expandingto 7–10 miles in the eastern part <strong>of</strong> the sea near the Korea Strait (Kun &Meshcheryakova, 1954; Kun, 1975). Currents may bring cladocerans to the open sea(Brodsky, 1955; Meshcheryakova, 1960; Miklukhina, 1967). Some species <strong>of</strong> the superorder(Pseudevadne tergestina, Podon leuckarti, Pleopis polyphemoides, and Peniliaavirostris) are indicators <strong>of</strong> coastal surface water conditions (Biryulin et al., 1970).In summer cladocerans may be abundant in the neritic zone. They are common and<strong>of</strong>ten dominate and subdominate in the plankton <strong>of</strong> Peter the Great Bay.Specimens for drawing some missing biological stages <strong>of</strong> four species <strong>of</strong> the podonids(Podon leuckarti, Pleopis polyphemoides, Evadne nordmanni, and Pseudevadnetergestina) were picked out from the plankton samples collected in 1996–2002in Vostok Bay (Peter the Great Bay) and in the south-western part <strong>of</strong> Peter the GreatBay.10
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- Page 42 and 43: Plate II. Nebalia bipes: 1 - distal
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8. Genus Exacanthomysis Holmquist,
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exopod with one simple lateral seta
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Mauchline, J. 1980. The biology of
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Plate II. Archaeomysis grebnitzkii
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Plate IV. Meterythrops robusta (1-4
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Plate VI. Xenacanthomysis pseudomac
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Plate VIII. Disacanthomysis dybowsk
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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