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Fiche d'espèce de Copépode |
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Cyclopoida ( Ordre ) |
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Oithonidae ( Famille ) |
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Oithona ( Genre ) |
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Oithona nana Giesbrecht, 1892 (F,M) | |
| | | | | | | Syn.: | ? Oithona helgolandica Claus, 1863 (p.105);
Oithonina nana : Sars, 1913 (1918) (p.5); Wilson, 1932 a (p.316, figs.F); 1942 a (p.197); 1950 (p.271); Fagetti, 1962 (p.40); Haq, 1965 a (p.555, figs. Nauplius, C1, key of Nauplius); Harder, 1968 (p156, Table 1, behaviour v.s. density discontinuity); Shih & al., 1971 (p.56);
Oithona plumosa Lindberg, 1947; 1950 e (p.265); Wellershaus, 1970 (p.480); Shuvalov, 1980 (p.152, figs.F);
O. plumosa pseudoplumosa Lindberg, 1950 e (p.265) | | | | Ref.: | | | Giesbrecht, 1892 (p.538, 549, 774, figs.F,M); Karavaev, 1894 (p.58, figs.F, Rem.); Thompson & Scott, 1903 (p.236, 255); Esterly, 1905 (p.209, figs.F,M); Burckhardt, 1913 (p.425); Rosendorn, 1917 a (p.40, figs. F,M); Pesta, 1920 (p.552); Murphy, 1923 (p.449, figs., key juv. stages); Sewell, 1924 (p.791); Früchtl, 1924 b (p.70); Gurney, 1927 (p.159, Rem.: 2 forms); Mori, 1929 (p.199, figs.F); Kiefer, 1929 g (p.9, Rem.F,M); Sewell, 1933 (p.30); Dakin & Colefax, 1933 (p.207); Rose, 1933 a (p.281, figs.F,M); Mori, 1937 (1964) (p.113, figs.F,M); Sewell, 1947 (p.254, Rem.); Marques, 1951 a (p.24); Carvalho,1952 a (p.167, figs.F); Marques, 1958 a (p.134); Tanaka, 1960 (p.59, figs.F,M, Rem.); Grice, 1960 a (p.487, figs.F,M); Vilela, 1965 (p.12); Gonzalez & Bowman, 1965 (p.272, figs.F,M); Vilela, 1968 (p.29); Ramirez, 1969 (p.88); Corral Estrada, 1970 (p.213, Rem.); Wellershaus, 1970 (p.479); Sazhina & Kovalev, 1971 (p.1100, fig.F); Björnberg, 1972 (p.88, figs., Rem.N); Razouls, 1972 (p.95, Annexe: p.104); Chen & al., 1974 (p.33, figs.F,M); Marques, 1975 (p.50); Nishida & al., 1977 (p.138, figs.F,M); Dawson & Knatz, 1980 (p.9, figs.F,M); Shuvalov, 1980 (p.146, figs.N,F,M); Ferrari & Bowman, 1980 (p.14, figs.F,M); Nishida, 1985 a (p.30, 52, Redescr. F,M, figs.F,M, Rem.: 2 forms, p.139); Björnberg & al., 1981 (p.665, figs.F,M); Dussart & Defaye, 1985 (p.10); Sazhina, 1985 (p.85, figs.N); Nishida, 1985 a (p.52, figs.F,M); 1986 (p.386); Huys & Boxshall, 1991 (p.205, 442, 465, figs.F,M); Kim & al., 1993 (p.271); Chihara & Murano, 1997 (p.937, Pl.198,203: F,M); Bradford-Grieve & al., 1999 (p.886, 966, figs.F); McKinnon, 2000 (p.108, Rem.); Conway & al., 2003 (p.203, figs.F,M, Rem.); Boxshall & Halsey, 2004 (p.612: figs.F); Conway, 2006 (p.21, copepodides 1-6, Rem.); Vives & Shmeleva, 2010 (p.65, figs.F,M, Rem.); Al-Yamani & al., 2011 (p.96, 98, figs.F,M) |  issued from : F.D. Ferrari & T.E. Bowman in Smiths. Contr. Zool., 1980, 312. [p.15, Fig.8]. Female (from Caribbean area): a, habitus (lateral right side); b, urosome (lateral right side); c, P4. Nota: Prosome/Urosome = 1.1. Endopodal segment 1 of P4 with a distinct row of 4 long spines Endopodal segment 2 of P4 with both setae mofified, neither seta strongly curved, both with flange on distal 3/5; endopodal segment 3 of P4 proximal seta similar, with flange on distal 3/5. P5 elongate , with several long hairs dorsal to it on posterior margin of urosomal segment 1. Knob near genital opening armed with short, thick spine and longer seta. Male: d, habitus (lateral right side); e, cephalosome and flap; f-g, left and right \"pore signature\" of second male; h-i, same of third male. Nota: Prosome/Urosome = 1.3. Flap of cephalosome relatively broader and shorter than in O. hebes and O. fonsecae; Anterodorsal cluster of \"pore signature\" roughtly circular. Intraspecific variation in the \"pore signature\" has been observed in this species.
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 Issued from : S. Nishida in Bull. Ocean Res. Inst., Univ. Tokyo, 1985, No 20. [p.56, Fig.27]. As Oithona nana typical form. Female: a, habitus (dorsal); b, forehead (lateral); c, thoracic segment 5 and genital segment (lateral left side); d, A1; e, Md (mandibular palp); f, Md (biting edge); g, mx1.
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 Issued from : S. Nishida in Bull. Ocean Res. Inst., Univ. Tokyo, 1985, No 20. [p.57, Fig.28]. As Oithona nana typical form. Female: a, anal segment and caudal rami (dorsal); b, A2; c, Mx2; d, Mxp; e, P1; f, P2; g, P3.
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 Issued from : S. Nishida in Bull. Ocean Res. Inst., Univ. Tokyo, 1985, No 20. [p.58, Fig.29]. As Oithona nana \"plumosa\" form. Female: a, habitus (dorsal); b, forehead (lateral); c, last thoracic segments and genital segment (dorsal); d, anal segment and caudal rami (dorsal); e, Md (mandibular palp); f, Mx1.
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 Issued from : S. Nishida in Bull. Ocean Res. Inst., Univ. Tokyo, 1985, No 20. [p.59, Fig.30]. As Oithona nana \"plumosa\" form. Female: a, A1; b, A2; c, Mx2; d, Mxp; e, P1; f, P2; g, P3; h, P4. Nota: after Vives & Shmeleva (2010, p.67): Setal formula on outer margin (in first) and inner margin (in second) of exopod segments (from proximal to distal) of P1 to P4: P1: 1, 1, 3; 1, 1, 4. P2: 1, 1, 3; 1, 1, 5 P3: 1, 1, 3; ; 1, 1, 5. P4: 1, 1, 2; 1, 1, 5.
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 Issued from : S. Nishida in Bull. Ocean Res. Inst., Univ. Tokyo, 1985, No 20. [p.61, Fig.31]. As Oithona nana \"plumosa\" form. Male: a, habitus (dorsal); b, forehead (lateral); c, last thoracic segments and genital segment (dorsal); d, thoracic segment 5 and genital segment (ventral); ; e, last urosomal segments and caudal rami (dorsal); f, Md (mandibular palp); g, Md (biting edge); h, Mx1; i, Mx2; j, Mxp.
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 Issued from : S. Nishida in Bull. Ocean Res. Inst., Univ. Tokyo, 1985, No 20. [p.62, Fig.32]. As Oithona nana \"plumosa\" form. Male: a, thoracic segment 5 and genital segment (lateral right side); b, A1; c, A2; d, P1; e, P2; f, P3; g, P4.
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 issued from : Q.-c Chen & S.-z. Zhang & C.-s. Zhu in Studia Marina Sinica, 1974, 9. [Pl.2, Figs.6-12]. Female (from China Seas): 6, habitus (dorsal); 7, forehead (lateral); 8, P1; 9, P2; 10, P3; 11, P4. Male: 12, habitus (dorsal).
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 issued from : C.O. Esterly in Univ. Calif. Publs Zool., 1905, 2 (4). [p.209, Fig.51]. Female (from San Diego): b, 3rd segment of exopod of P1. Male: a, habitus (dorsal); c, 3rd segment of exopod of P4.
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 issued from : G.D. Grice in Bull. mar. Sci. Gulf Caribb., 1960, 10 (4). [p.486, Figs.7-11]. Female (from NE Gulf of Mexico: off Alligator Harbor): 7, habitus (dorsal); 8, forehead (lateral); 9, P4. Nota: Rostrum absent. Exopod segments of P4 with 1, 1, 2 spines. Male: 10, habitus (dorsal); 11, basipodal segment 2 of Md. Nota: Exopod segments of P1 with 1, 1, 2 spines; 2nd basipodal segment of Md with 1 strong and 1 fine seta.
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 issued from : I. Rosendorn in Wiss. Ergebn. dt. Tiefsee-Exped. \"Valdiviella\", 1917, 23. [p.41, Fig.24]. Female: a, habitus (dorsal); b, Mx1. Nota: Proportion of lengths (p.cent) Prosome : 54.72, Urosome : 45.28 . Relative lengths of urosomal segments and caudal rami: 10 : 33 : 17 : 17 : 13 : 13. Setal formula of the exopod swimming legs P1 to P4 (Se = outer setae ; Si = inner setae), P1 : 1, 1, 3 Se ; 1, 1, 4 Si ; P2 : 1, 1, 3 Se ; 1, 1, 5 Si ; P3 : 1, 1, 3 Se ; 1, 1, 5 Si ; P4 : 1, 1, 1 Se ; 1, 1, 5 Si . Male: c, urosome; d, Md. Nota: Proportion of lengths (p.cent) Prosome : 56.82, Urosome : 43.18 . Relative lengths of urosomal segments and caudal rami: 7 : 10 : 9 : 7: 6 : 4 : 4. Setal formula of the exopod swimming legs P1 to P4 (Se = outer setae ; Si = inner setae), P1 : 1, 1, 3 Se ; 1, 1, 4 Si ; P2 : 1, 1, 3 Se ; 1, 1, 5 Si ; P3 : 1, 1, 3 Se ; 1, 1, 5 Si ; P4 : 1, 1, 2 Se ; 1, 1, 5 Si .
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 issued from : T. Mori in Zool. Mag. Tokyo, 1929, 41 (486-487). [Pl. VII, Figs. 11-12]. Female (from Chosen Strait, Korea-Japan); 11, P1; 12, habitus (dorsal).
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 issued from : T. Mori in The Pelagic copepoda from the neighbouring waters of Japan, 1937 (1964). [Pl. 63, Figs.1, 3-8]. Female: 1, habitus (dorsal); 3, Md; 4, P1; 5, P2; 6, P3; 7, P4; 8, Mx1.
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 issued from : T. Mori in The Pelagic copepoda from the neighbouring waters of Japan, 1937 (1964). [Pl. 63, Fig.2]. Male: 2, habitus (dorsal).
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 issued from : V.S. Shuvalov in Opred. Faune SSSR, Nauka, Leningrad, 1980, 125. [p.147, Fig.41]. Female: A-B, habitus (dorsal and lateral, respectively); C, habitus (dorsal); D, forehead (dorsal); E, cephalon (lateral); F, 4th, 5th toracic segments and genital segment (dorsal); G, posterior part of abdomen and caudal rami; H, P1; I, P2; J, P3; K, P4.
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 issued from : V.S. Shuvalov in Opred. Faune SSSR, Nauka, Leningrad, 1980, 125. [p.153, Fig.44]. As Oithona plumosa. After Lindberg, 1950. Female: A, habitus (dorsal); B, forehead (dorsal); C, same (ventral); D, same (lateral); E, A1; F, A2; G, Md; H, posterior part of urosome.
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 Issued from : W. Giesbrecht in Systematik und Faunistik der Pelagischen Copepoden des Golfes von Neapel und der angrenzenden Meeres-Abschnitte. – Fauna Flora Golf. Neapel, 1892, 19 , Atlas von 54 Tafeln. [Taf.44, Figs.2, 4]. Male: 2, habitus (dorsal); 4, forehead (lateral). Ce = cephalosome.
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 Issued from : W. Giesbrecht in Systematik und Faunistik der Pelagischen Copepoden des Golfes von Neapel und der angrenzenden Meeres-Abschnitte. – Fauna Flora Golf. Neapel, 1892, 19 , Atlas von 54 Tafeln. [Taf.44, Fig.6]. Male: 6, urosome (dorsal).
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 Issued from : W. Giesbrecht in Systematik und Faunistik der Pelagischen Copepoden des Golfes von Neapel und der angrenzenden Meeres-Abschnitte. - Fauna Flora Golf. Neapel, 1892, 19 , Atlas von 54 Tafeln. [Taf. 34, Figs.10, 11, 20]. Female: 10, head (lateral); 11, forehead (dorsal); 20, urosome (dorsal). Th5 = thoracic segment 5; Ab 1-2 = genital double-somite; Ab 5 = anal somite; Se = outer marginal seta.
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 Issued from : W. Giesbrecht in Systematik und Faunistik der Pelagischen Copepoden des Golfes von Neapel und der angrenzenden Meeres-Abschnitte. - Fauna Flora Golf. Neapel, 1892, 19 , Atlas von 54 Tafeln. [Taf. 34, Figs.24, 26]. Female: 24, Md; 26, Mx1. B2 = basis; Ri = endopodite; Li 3 = inner lobe 3.
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 Issued from : W. Giesbrecht in Systematik und Faunistik der Pelagischen Copepoden des Golfes von Neapel und der angrenzenden Meeres-Abschnitte. - Fauna Flora Golf. Neapel, 1892, 19 , Atlas von 54 Tafeln. [Taf. 34, Figs.34, 35, 42]. Female: 34, P1; 35, P2; 42, P4.
| | | | | Ref. compl.: | | | Cleve, 1904 a (p.192); Carazzi & Grandori, 1912 (p.14, 38); Rose, 1925 (p.152); Massuti Alzamora, 1942 (p.102, Rem.); Sewell, 1948 (p.367, 461, 487); Fleury, 1950 (p.47, fig.2); Hansen K.V., 1951 (p.231, migration v.s. discontinuity layer); Grice, 1956 (p.61); Yamazi, 1958 (p.153, Rem.); Gaudy, 1962 (p.93, 99, Rem.: p.116) ; Ganapati & Shanthakumari, 1962 (p.10, 16); Shmeleva, 1963 (p.141); Duran, 1963 (p.25); Giron-Reguer, 1963 (p.56); Gaudy, 1963 (p.30, Rem.); Björnberg, 1963 (p.75, Rem.); Unterüberbacher, 1964 (p.32); De Decker, 1964 (p.16, 23, 29, 32); De Decker & Mombeck, 1964 (p.13); Shmeleva, 1965 b (p.1350, lengths-volume -weight relation); Neto & Paiva, 1966 (p.30, Table III, annual cycle); Pavlova, 1966 (p.44); Chakroun, 1966 (p.67, Tableau); Mazza, 1966 (p.73); 1967 (p.363); Ehrhardt, 1967 (p.742, geographic distribution, Rem.); Delalo, 1968 (p.138); Porumb, 1968 (p.417); Dimov, 1968 (p.506); Kovalev, 1968 a (p.441, fig.1); Emery, 1968 (p.293, swarm); Champalbert, 1969 a (p.642); El-Maghraby & Dowidar, 1970 (p.81); Dowidar & El-Maghraby, 1970 (p.269); Reeve, 1970 (p.894, Rem.: p.908); Carli, 1971 (p.372, tab.1); Paulmier, 1971 (p.168); Salah, 1971 (p.320); Apostolopoulou, 1972 (p.329, 373); Valentin, 1972 (p.349, egg production); Binet, 1973 (p.77); Corral Estrada & Pereiro Muñoz, 1974 (tab.I); Hirota, 1974 (p.1, Table 3, 4, fig.4, 5, 6); Hirota & Hara, 1975 (p.115, fig.5); Vives & al., 1975 (p.53, tab.II, III, IV); Porumb, 1976 (p.91); Lakkis & Abboud, 1976 (p.81); Newbury & Bartholomew, 1976 (p.373, production); Gaudy, 1976 (p.77, fig.1, 7, Table I, II, III, production); Furuhashi, 1976 (p.355, Diel vertical migration); Hanaoka, 1977 (p.267, 301, abundance); Ferrari, 1977 (p.410); Boxshall, 1977 b (p.553); Grindley, 1977 (p.341, Table 2); Dessier, 1979 (p.83, 201, 207); Vaissière & Séguin, 1980 (p.23, tab.2); Gallo, 1981 (p.847); Castel & Courties, 1982 (p.417, Table II, fig.4, spatial & monthly distribution); Vives, 1982 (p.295); Lampitt & Gamble, 1982 (p.183, respiration v.s. food); Kovalev & Shmeleva, 1982 (p.85); Scotto di Carlo & al., 1984 (p.1045); Dussart, 1984 (p.301); Patriti & al., 1984 (tab.1); Regner, 1985 (p.11, Rem.: p.40); ); Jansa, 1985 (p.108, Tabl.I, II, III, IV, V); Garcia-Rodriguez, 1985 (p.37); 1985 a (p.41, 42); M. Lefèvre, 1986 (p.33); Diouf & Diallo, 1987 (p.260); Lozano Soldevilla & al., 1988 (p.61); Krsinic & Vilicic, 1989 (p.12, tab.3); Krsinic, 1990 (p.337, Table III, vertical distribution)Dai & al., 1991 (tab.1); Yoo, 1991 (tab.1); Jouffre & al., 1991 (p.489, lagoon); Santos & Ramirez, 1991 (p.83); Seguin & al., 1993 (p.23); Guerin-Ancey & David, 1993 (p.119, table 1, biovolume, vertical distribution); Santos & Ramirez, 1995 (p.133, Tabl. I, fig.2, 3); Shih & Young, 1995 (p.75); Böttger-Schnack, 1995 (p.92); 1996 (p.1088); Kotani & al., 1996 (tab.2); Böttger-Schnack, 1997 (p.410); Park & Choi, 1997 (Appendix); Sharaf & Al-Ghais, 1997 (tab.1); Hure & Krsinic, 1998 (p.76, 103); Gilabert & Moreno, 1998 (tab.1,2); Hopcroft & al., 1998 (tab.2); Alvarez-Cadena & al., 1998 (t.4); Suarez-Morales & Gasca, 1998 a (p.111); Omori & Norman, 1998 (p.279, Rem.: anthropogenic short-term effects); Siokou-Frangou, 1999 (p.478); Lavaniegos & Gonzalez-Navarro, 1999 (p.239, Appx.1); Lopes & al., 1999 (p.215, tab.1); Neumann-Leitao & al., 1999 (p.153, tab.2); Dolganova & al., 1999 (p.13, tab.1); Ueda & al., 2000 (tab.1); Seridji & Hafferssas, 2000 (tab.1); Holmes Gotto, 2000 (p.4, Rem.); Sautour & al., 2000 (p.531, Table II, abundance); d'Elbée, 2001 (tabl.1); Richard & Jamet, 2001 (p.957: Rem.); Fransz & Gonzalez, 2001 (p.255, tab.1); El-Serehy & al., 2001 (p.119, tab.1, 3, 4); Bressan Moro, 2002 (tab.2); Sameoto & al., 2002 (p.13); Zerouali & Melhaoui, 2002 (p.91, Tableau I, figs.5, 8); Dunbar & Webber, 2003 (tab.1); Vukanic, 2003 (p.139, tab.1); McKinnon & al., 2003 (p.101, tab.2, fig.11); Zagorodnyaya & al., 2003 (p.52); Rezai & al., 2004 (p.486, tab.2, 3, abundance); Chang & Fang, 2004 (p.456, tab.1); Daly Yahia & al., 2004 (p.366, fig.4, tab.1); Fernandez de Puelles & al., 2004 (p.654, fig.7); Marrari & al., 2004 (p.667, tab.1); Vukanic & Vukanic, 2004 (p.361, tab.3, fig.3); Guermazi & al., 2005 (p.280); Mazzochi & al., 2005 (p.155); Licandro & al., 2005 (p.153); Lakkis & al., 2005 (p.152); Alvarez-Silva & al., 2005 (p.39); Rawlinson & al., 2005 (p.205, tidal exchange); Prusova & Smith, 2005 (p.76, 78); Zuo & al., 2006 (p.164: tab.1); Isari & al., 2006 (p.241, tab.II); Marques & al., 2006 (p.297, tab.III); Mageed, 2006 (p.471, Tabl.2, 4); Williams & Muxagata, 2006 (p.1055); Atienza & al., 2006 (p.221]; Albaina & Irigoien, 2007 (p.435: Tab.1); Porri & al., 2007 (p.714); David & al., 2007 (p.59: tab.2); Busatto, 2007 (p.26, Tab.2); Valdés & al., 2007 (p.104: tab.1); Krsinic & al., 2007 (p.528); Leandro & al., 2007 (p.215); McKinnon & al., 2008 (p.843: Tab.1, p.846: Tab.II, fig.7); Isinibilir & al., 2008 (p.745: Tab.1); Cabal & al., 2008 (289, Table 1) ; Humphrey, 2008 (p.84: Appendix A); Neumann-Leitao & al., 2008 (p.799: Tab.II, fig.6); Morales-Ramirez & Suarez-Morales, 2008 (p.514); Selifonova & al., 2008 (p.305, Tabl. 2); Shmeleva & al., 2008 (p.31, Table 1); Rossi, 2008 (p.90: Tableau XII); Ohtsuka & al., 2008 (p.115, Table 5); Miyashita & al., 2009 (p.815, Tabl.II); Brylinski, 2009 (p.253: Tab.1, p.256: Rem.); Hafferssas & Seridji, 2010 (p.353, Table 2); Lidvanov & al., 2010 (p.356, Table 3); Drira & al., 2010 (p.145, Tanl.2); Hernandez-Trujillo & al., 2010 (p.913, Table 2); Hidalgo & al., 2010 (p.2089, Table 2); Mazzocchi & Di Capua, 2010 (p.428); Medellin-Mora & Navas S., 2010 (p.265, Tab. 2); Fazeli & al., 2010 (p.153, Table 1); Hsiao S.H. & al., 2011 (p.475, Appendix I); Salah S. & al., 2011 (Tableau 1); Maiphae & Sa-ardrit, 2011 (p.641, Table 2, 3, Rem.); Saitoh & al., 2011 (p.85, Table 4, 5); Magris & al., 2011 (p.260, abundance, interannual variability); Moscatello & al., 2011 (p.80, Table 4); Cepeda & al., 2012 (p.1, figs.1, 3, Table 1, Molecular systematic); Van Ginderdeuren & al., 2012 (p.3, Table 1); Delpy & al., 2012 (p.1921, Table 2, fig.7); Shiganova & al., 2012 (p.61, fig. 4, 5); Glushko & Lidvanov, 2012 (p.138, Tableau 1) ; Uysal & Shmeleva, 2012 (p.909, Table I); DiBacco & al., 2012 (p.483, Table S1, ballast water transport); Zizah & al., 2012 (p.79, Tableau I, Rem.: p.86); Zamora-Terol & Saiz, 2013 (p.376, Rem.: Table 3, egg production) | | | | NZ: | 20 | | | | | | | | | | | | | | |  Issued from : S. Nishida in Bull. Ocean Res. Inst., Univ. Tokyo, 1985, No 20. [p.139, Fig.90].
Indo-Pacific geographical distribution of Oithona nana. Dotted line: AC, Arctic Convergence; SC, Subtropical Convergence. Arrows indicate stations where the \"plumosa\" form occurred. |
 issued from : A.A. Shmeleva in Bull. Inst. Oceanogr., Monaco, 1965, 65 (n°1351). [Table 6: 39]. Oithona nana (from South Adriatic).
Dimensions, volume and Weight wet. Means for 50-60 specimens. Volume and weight calculated by geometrical method. Assumed that the specific gravity of the Copepod body is equal to 1, then the volume will correspond to the weight. |
 issued from : M.R. Reeve in Bull. mar. Sc., 1970, 20 (4). [p.902, Fig.4].
Temperature-salinity diagram for Oithona nana in Biscayne Bay (Florida, Miami). |
 issued from : A.V. Bogorov in Gidrobiol. Zh., 1968 4 (3). [p.78, Table 1].
Number of egg-laying from the same body size at different seasons in the Black Sea.
A: Month and year; B: Females number analysed; C: Body lengths (limits of variation; M = mean); D: Number of eggs. |
 issued from : A.V. Bogorov in Gidrobiol. Zh., 1968 4 (3). [p.79, Table 2, 3].
Table 2: Importance of number eggs-laying by female of the same body size from the Black Sea and the Mediterranean Sea.
A: Sea; B: Month and Year; C, Body size of females (limits and M = mean); D: Number of eggs (M = mean).
Table 3: Number of eggs by female and body sizes.
A: Lengths in mm; B: Number of eggs. |
 issued from : A.V. Bogorov in Gidrobiol. Zh., 1968 4 (3). [p.79, Fig.3 1].
Relation between the body of females and the egg diameter.
Black circle: Black Sea; open circle: Mediterranan Sea and Adriatic Sea. |
| | | | Loc: | | | Afr. S (E & W), Saldanha Bay, Namibie, Angola, Baia Farta, Rio Congo estuary, G. de Guinée, Casamance, Is. du Cap Vert, off Maroc-Mauritanie, Cap Ghir, Canaries, off Madère, Portugal, G. de Gascogne, off Gironde estuary, la Pallice roadstead, Arcachon Bay, Glenans Islands, Belon estuary, Buenos Aires, Peninsula Valdés, off Mar del Plata, Brésil (S, Mucuri estuary, off Natal), I. Barbade, Caribbean Colombia (Guajira, Tayrona)); Yucatan, E Costa Rica, G. du Mexique, Porto Rico, Jamaïque (Kingston Harbour), Cuba, Floride, Bermuda, Woods Hole, off Nova Scotia E, off Terre-Neuve, Islande S, Irlande, Lough Hyne, Scotland (Loch Thurnaig), Manche, Strait of Dover (near the coast south of Boulogne), Mer du Nord, Oslo fjord, Baie Ibéro-marocaine, Médit. (Mer d'Alboran, laguna Mar Menor, Castellon, Baleares, Banyuls, Etang de Thau, Etang de Berre, Marseille, Toulon harbour, Villefranche-s-Mer, Gênes, Mer Tyrrhénienne, Naples, Tunisie (Sfax, G. of Gabès), Ionienne, Adriatique, Vlora Bay, Mljet Is., Venise, Po delta, Port of Koper; Mer Egée, Marmara Sea, Black Sea, Sebastopol, , Black River estuary, Iskenderoun Bay, Levantin Basin, Alexandrie, Bardawill Lagoon), Canal de Suez, Mer Rouge, Gulf of Oman, Mer Arabe, Arabian Gulf, Kuwait, Ceylan, Madagascar (Nosy Bé), Rodrigues Is., Indien, Inde (Lawson's Bay), Chilka Lake, Kurau Riv., I. Christmas, Nicobar Is., Straits of Malacca, G. of Thailand, Indonésie-Malaisie, Viet-Nam, mers de Chine (Bohai Sea, Yellow Sea, East China Sea, South China Sea, Xiamen Harbour), Taiwan (Kaohsiung Harbor, Kuroshio Current), Corée S, Mer du Japon, Maizuru Bay, Japan, Seto Inland Sea, Ariake-kai, Yatsushiro-kai, Tanabe Bay, Kouriles, Palau Is., Pacif. tropical, Hawaii, Californie (San Pedro, San Diego), Basse Californie (Bahia Magdalena), G. de Californie, Zihuatanejo Bay, Mexique W, Is. Fidji, Is. Samoa, Australie (North West Cape, Nouvelle-Galles du Sud), Nouvelle-Calédonie, Nouvelle-Zélande, I. Moorea, Pacif. SE, off Chili, Chili (N) | | | | N: | 276 | | | | Lg.: | | | (11) F: 0,56; (45) F: 0,65-0,5; M: 0,57-0,48; (46) F: 0,53-0,5; M: 0,5-0,48; (66) F: 0,64-0,51; M: 0,55; (91) F: ± 0,62; M: ± 0,54; (109) F: 0,65-0,5; M: 0,55-0,45; (142) F: 0,8-0,7; M: 0,6-0,5; (155) F: 0,62-0,54; M: 0,51-0,48; (179) F: 0,66-0,6; M: 0,55-0,45; (237) F: 0,55-0,6; M: 0,40; (327) F: 0,68-0,55; M: 0,57-0,56; (373) F: 0,73-0,49; M: 0,61-0,48; (432) F: 0,95-0,55; (434) F: 0,65-0,42; M: 0,49-0,45; (449) F: 0,53-0,5; M: 0,5-0,48; (579) M: 0,63-0,54; (618) F: 0,63-0,42; M: 0,48-0,45; (624) F: 0,72-0,58; M: 0,53-0,47; (627) F: 0,59-0,49; 0,53-0,49; M: 0,48-0,47; (649) F: 0,53; M: 0,44; (651) F: 0,67-0,57; (786) F: 0,62; (880) F: 0,50-0,70; M: 0,44-0,60; F: 0,44-0,60; (991) F: 0,5-0,8; M: 0,48-0,6; (1085) F: 0,48-0,6; M: 0,45-0,5; (1302) F: 0,310-0,335; M: 0,301-0,336; {F: 0,31-0,95; M: 0,30-0,63} | | | | Rem.: | euryhaline. Epipélagique; neritic, Estuaries, coastal, harbors.
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Oithona nana Form plumosa Nishida,1985 (F)
Ref.: Nishida, 1985 a (p.55, Descr.F,M, figs.F)
Ref. compl.: Razai & al., 2004 (p.490, tab.2, Rem.)
Loc.: G. Arabe, Sri-Lanka, Straits of Malacca, G. de Thaïlande, Nouvelle-Calédonie
Voir aussi les remarques en anglais | | | Dernière mise à jour : 21/05/2013 | |
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 Toute utilisation de ce site pour une publication sera mentionnée avec la référence suivante :
Razouls C., de Bovée F., Kouwenberg J. et Desreumaux N., 2005-2012. - Diversité et répartition géographique chez les Copépodes planctoniques marins. Disponible sur http://copepodes.obs-banyuls.fr
[Accédé le 24 mai 2013] © copyright 2005-2012 CNRS, UPMC
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