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Fiche d'espèce de Copépode |
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Calanoida ( Ordre ) |
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Calanoidea ( Superfamille ) |
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Calanidae ( Famille ) |
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Mesocalanus ( Genre ) |
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Mesocalanus tenuicornis (Dana, 1849) (F,M) | |
| | | | | | | Syn.: | Calanus tenuicornis Dana,1849; Giesbrecht, 1892 (p.90, 129, figs.F,M); Giesbrecht & Schmeil, 1898 (p.18); Cleve, 1904 a (p.186); Esterly, 1905 (p.127, figs.M, Rem.F,M); Farran, 1908 b (p.20); A. Scott, 1909 (p.8); Sewell, 1914 a (p.193); Pesta, 1920 (p.496); Farran, 1926 (p.227); 1929 (p.207, 217); Sewell, 1929 (p.20); Mori, 1929 (p.170, Figs.F,M); Rose, 1929 (p.8); 1933 a (p.62, figs.F,M); Dakin & Colefax, 1933 (p.204); Farran, 1936 a (p.77); Mori, 1937 (1964) (p.16, figs.F,M); Dakin & Colefax, 1940 (p.87, figs.F,M); Vervoort, 1946 (p.22, Rem.); Sewell, 1948 (p.347, 513, 519, 544, 555, 565); Brodsky, 1950 (1967) (p.96, figs.F,M); C.B. Wilson, 1950 (p.269); Vervoort, 1951 (n°32, p.3, figs.F,M); Bowman, 1955 (p.413, figs.F,M, Rem.); Tanaka, 1956 (p.255); Chiba & al., 1957 (p.306); 1957 a (p.11); Yamazi, 1958 (p.146); Gaudy, 1962 (p.93, 99, Rem.: p.101); Grice, 1962 (p.175, Rem.); Ahlstrom & Thrailkill, 1963 (p.57, Table 5, abundance); V.N. Greze, 1963 a (tabl.2); Shmeleva, 1963 (p.141); Björnberg, 1963 (p.10, Rem.); Kasturirangan, 1963 (p.10, figs.F,M); Unterüberbacher, 1964 (p.13); De Decker, 1964 (p.14, 18, 29); De Decker & Mombeck, 1964 (p.11); Grice & Hulsemann, 1965 (p.223); Chen & Zhang, 1965 (p.28, figs.F,M); Shmeleva, 1965 b (p.1350, lengths-volume -weight relation); Pavlova, 1966 (p.43); Fleminger, 1967 a (tabl.1); Ehrhardt, 1967 (p.737, 887, figs.51-53, geographic distribution), Rem.); Grice & Hulsemann, 1967 (p.13); Delalo, 1968 (p.137); Vilela, 1968 (p.7, fig.M); Vidal, 1968 (p.14, figs.F); De Decker, 1968 (p.45); Park, 1968 (p.532, Rem.); Mullin, 1969 (p.438, biogéo); Park, 1970 (p.474); Morris, 1970 (p.2300); Corral Estrada, 1970 (p.64, figs.F,M); Dowidar & El-Maghraby, 1970 (p.267); Deevey, 1971 (p.224); Marshall & Orr, 1972 (p.8); Brodsky, 1972 (1975) (p.9, 69, 85, 121, figs.); Bradford, 1972 (p.31, fig.F); Razouls, 1972 (p.91, Tableau XXVI, XXVII, Annexe: p.5, figs.F,M); Boucher & Thiriot, 1972 (p.47, Tableau 4); Grice, 1972 (p.175); Roe, 1972 (p.277, tabl.1, tabl.2); 1972 a (p.318); Heinrich, 1973 (p.95); Björnberg, 1973 (p.287, 384); Corral Estrada & Pereiro Muñoz, 1974 (tab.I); Harding, 1974 (p.141, tab.3, gut contents); Peterson & Miller, 1975 (p.650); Vives & al., 1975 (p.35, tab.II, III, IV); Vyshkvartzeva, 1976 (p.14); 1977 a (p.97, figs.); Carter, 1977 (1978) (p.35); Deevey & Brooks, 1977 (p.256, Table 2, Station "S"); Dawson & Knatz, 1980 (p.5, F,M); Sreekumaran Nair & al., 1981 (p.493), Björnberg & al., 1981 (p.616, figs.F,M); Brenning, 1981 (p.1, Rem.: p.4); Kovalev & Shmeleva, 1982 (p.82); Alvarez-Marques, 1984 (p.112, figs.F,M); De Decker, 1984 (p.315, 332: carte); Scotto di Carlo & al., 1984 (p.1042); Cummings, 1984 (p.163, Table 2); Brenning, 1985 a (p.3, Table 2); Regner, 1985 (p.11, Rem.: p.22); Ambler & Miller, 1987 (tab.2, 3, 4, 5); Lozano Soldevilla & al., 1988 (p.57); Jimenez-Perez & Lara-Lara, 1988; Hernandez-Trujillo, 1989 a (tab.1); Suarez & al., 1990 (tab.2); Valdes & al., 1990 (tab.2); Scotto di Carlo & al., 1991 (p.271); Yoo, 1991 (tab.1); Suarez & Gasca, 1991 (tab.2); Morales C.E. & al., 1991 (p.455, Table I, grazing); Rosales & Sepulveda, 1992 (p.38); Ayukai & Hattori, 1992 (p.163, Table 5, fecal pellet production rate); Suarez, 1992 (App.1); Ashjian & Wishner, 1993 (p.483, abundance, species group distributions); Morales C.E. & al., 1993 (p.185); Seguin & al., 1993 (p.23); Landry & al., 1994 (p.55, abundance, grazing); Hays & al., 1994 (tab.1); Suarez-Morales, 1998 (p.345, Table 1); Moraitou-Apostolopoulou & al., 2000 (tab.I); Sautour & al., 2000 (p.531, Table II, abundance); Weikert & al., 2001 (p.227, tab.4, Rem.); Hernandez-Trujillo & Esqueda-Escarcega, 2002 (in Appendix); Vukanic, 2003 (p.139, tab.1); Vukanic & Vukanic, 2004 (p.9, tab. 2, 3); Maiphae & Sa-ardrit, 2011 (p.641, Table 2);
Neocalanus tenuicornis : Sars, 1925 (p.9); Wilson, 1942 a (p.195); Lysholm & al., 1945 (p.7); C.B. Wilson, 1950 (p.269); Brodsky, 1962 c (p.98); Fagetti, 1962 (p.7); Chen & Zhang, 1965 (p.28, figs.F,M); Mazza, 1966 (p.69); Brodsky, 1972 (1975) (p.116); Vives & al., 1975 (p.35, tab.II); Zheng & al., 1982 (p.7, figs.F,M); Brodsky & al., 1983 (p.185, figs.F,M); Guangshan & Honglin, 1984 (p.118, tab.); Kouwenberg, 1994 (tab.1); Go & al., 1997 (tab.1); Park & Choi, 1997 (Appendix); Hure & Krsinic, 1998 (p.15, 99); Padmavati & al., 1998 (p.349); Hwang & al., 1998 (tab.II); Mauchline, 1998 (tab.30); Bragina, 1999 (p.195); Ashjian & al., 2005 (p.1380: tab.2); Gaard & al., 2008 (p.59, Table 1, N Mid-Atlantic Ridge); Pagano, 2009 (p.115); Selifonova, 2011 (p.77, Table 1, alien species in Black Sea); | | | | Ref.: | | | Bradford & Jillett, 1974 (p.12, figs.F,M); Gardner & Szabo, 1982 (p.148, figs.F,M); Mackas & Sefton, 1982 (p.1179); Fleminger, 1985 (p.276, 285, Table 1, 4, fig.M, Rem.: A1); Bradford,1988 (p.74, 76); Bradford-Grieve, 1994 (p.38, figs.F,M, Rem., fig.98); Chihara & Murano, 1997 (p.741, Pl.69: F,M); Bradford-Grieve & al., 1999 (p.877, 907, figs.F,M); Bucklin & al., 2003 (p.335, tab.2, fig. 4, Biomol.); Conway & al., 2003 (p.147, figs.F,M, Rem.); Boxshall & Halsey, 2004 (p.81: fig.M); Vives & Shmeleva, 2007 (p.898, figs.F,M, Rem.) |  issued from : J.M. Bradford-Grieve in The Marine Fauna of New Zealand: Pelagic Calanoid Copepoda. National Institute of Water and Atmospheric Research (NIWA). New Zealand Oceanographic Institute Memoir, 102, 1994. [p.39, Fig.14]. Female: A, habitus (dorsal); B, idem (right lateral side); C, P5. Nota: Li 1 of Mx2 with 4 setae. Endopodite 1 of P1 without inner seta. Endopodite of P5 with 7 setae. Male: D, habitus (dorsal); E, P5. Nota: Left P5 slightly modified, not prehensile. Exopodite 1 of P2 without recurved spine (hook) adjacent to outer spine. Coxa of P5 with inner edge without teeth. Both endopodite of P5 with 7 setae each.
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 issued from : J.M. Bradford & J.B. Jillett in Crustaceana, 1974, 27 (1). [p.14, Fig.2,G,M]. Female: G, P5. Male: M, P5 (L = left, R = right).
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 issued from: Q.-c Chen & S.-z. Zhang in Studia Marina Sinica, 1965, 7. [Pl.2, 4-8]. As Neocalanus tenuicornis. Female (from E China Sea): 4, habitus (dorsal); 5, idem (lateral right side); 6, endopod of P1 (anterior). Male: 7, habitus (dorsal); 8, left P5 (posterior).
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 issued from : J. Corral Estrada in Tesis Doct., Univ. Madrid, A-129, Sec. Biologicas, 1970. [Lam.4]. As Calanus tenuicornis. Female (from Canarias Is.): 1, habitus (dorsal); 2, urosome (ventral). Male: 3, habitus (dorsal); 4, P5.
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 issued from : W. Giesbrecht in Fauna Flora Golf. Neapel, 1892, 19. [Taf.8, Fig.27]. As Calanus tenuicornis. Male: 27, P5 (anterior surface).
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 issued from : W. Giesbrecht in Fauna Flora Golf. Neapel, 1892, 19. [Taf.8, Fig.18]. As Calanus gracilis. Female; 18, P5 (anterior surface). B1 = basipodite 1 (= Coxa); B2 = basiopodite 2 (= Basis): Re = exopodite; Ri = endopodite.
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 issued from : T. Mori in The pelagic Copepoda from the neighbouring waters of Japan, 1937 (1964). [Pl.3, Figs.9-10]. As Calanus tenuicornis. Female: 9, P5 (posterior); 10, P1 (anterior).
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 issued from : T. Mori in The pelagic Copepoda from the neighbouring waters of Japan, 1937 (1964). [Pl.4, Figs.1-3]. As Calanus tenuicornis. Female: 2, habitus (lateral). Male: 1, habitus (dorsal); 3, P5.
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 issued from : Z. Zheng, S. Li, S.J. Li & B. Chen in Marine planktonic copepods in Chinese waters. Shanghai Sc. Techn. Press, 1982 [p.8, Fig.2]. As Neocalanus tenuicornis. Female: a-b, habitus (dorsal and lateral, respectively); c, P1; d, P3; e, P5. Male: f, habitus (dorsal); g, urosome (dorsal); h, head (lateral); i, P1; j, P5. Scale bars in mm.
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 issued from : J.M. Bradford in Mem. N. Z. Oceonogr. Inst., 1972, 54. [p.33, Fig.4 (4)]. Female (from Kaikoura, New Zealand): 4, habitus (lateral). Nota: Proportional lengths of abdominal segments 2 and 3: 4.8:3.8. Scale bar: 1 mm.
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 issued from T. Mori inZool. Mag. Tokyo, 1929, 41 (486-487). [Pl. III, Figs.20-23]. As Calanus tenuicornis. Female (from Chosen Strait, Korea-Japan): 20, urosome; 21, P2; 22, P3; 24, P5.
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 issued from T. Mori inZool. Mag. Tokyo, 1929, 41 (486-487). [Pl. IV, Fig.1]. As Calanus tenuicornis. Female: 1, A1.
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 issued from : A. Fleminger in Mar. Biol., 1985, 88. [p.284, Fig.6, G]. Male (NE, SE Pacific): Left A1 proximal segments (ventral view); Nota: see remarks in Calanus s.l. pacificus californicus (Fleminger, 1985, p.275) concerning the dimorphism in the female A1.
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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.6, Fig.13]. As Calanus tenuicornis. Female: 13, habitus (dorsal). Ce = cephalothorax; Th = thoracic segment; Ab1-2 = urosomal segment 1 (genital segment: = genital double-somite).
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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.6, Fig.12]. As Calanus tenuicornisMale: 12, habitus (dorsal). Ce = cephalothorax; Th1 = thoracic segment 1; Ab 5 = anal segment.
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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.7, Fig.5]. As Calanus tenuicornisFemale: 5, masticatory edge of Md (anterior view).
| | | | | Ref. compl.: | | | Mackas & Sefton, 1982 (p.1173, Table 1); Vives, 1982 (p.290); Tremblay & Anderson, 1984 (p.4); Roe, 1984 (p.356); Cooney & Coyle, 1985 (p.310); Wishner & Allison, 1986 (tab.2); Madhupratap & Haridas, 1986 (p.105, tab.1); Hirakawa & al., 1990 (tab.3); Hirakawa, 1991 (p.376: fig.2); Shih & Marhue, 1991 (tab.2, 3); Hattori, 1991 (tab.1, Appendix); Hirakawa & al., 1995 (tab.2); Shih & Young, 1995 (p.68); Kotani & al., 1996 (tab.2); Siokou-Frangou, 1997 (tab.1); Suarez-Morales & Gasca, 1997 (p.1525); Alvarez-Cadena & al., 1998 (t.4); Suarez-Morales & Gasca, 1998 a (p108); Kovalev & Piontkovski, 1998 (p.214, 217, Rem.); Dolganova & al., 1999 (p.13, tab.1); Goldblatt & al., 1999 (p.2619, tabl. 2); Razouls & al., 2000 (p.343, Appendix); Seridji & Hafferssas, 2000 (tab.1); Haury & al., 2000 (p.69, Table 1, Fig.7); Mackas & al., 2001 (p.685, Tab. 3, 6, fig.3: interannual changes in species composition); Rebstock, 2001 (tab.2); 2002 (p.71, Table 3, 5, Fig.2, climatic variability); Holmes, 2001 (p.38); Peterson & al., 2002 (p.353); Beaugrand & al., 2002 (p.1692); Beaugrand & al., 2002 (p.179, fig.5, 6); Yamaguchi al., 2002 (p.1007, tab.1); Mackas & Galbraith, 2002 (p.725, tab.2a, 2b); 2002 a (p.423, Table 2); Bode & al., 2003 (p.85, Table 1, abundance); Shimode & Shirayama, 2004 (tab.2); Hsiao & al., 2004 (p.325, tab.1); Hsieh & al. 2004 (p.397,tab. 1); Daly Yahia & al., 2004 (p.366, fig.1); CPR, 2004 (p.56, fig.163); Lo & al., 2004 (p.89, tab.1); Fernandez & al., 2004 (p.501, tab.5); Shimode & al., 2005 (p.113 + poster); Mackas & al., 2004 (p.875, Table 2); Mackas & al., 2005 (p.1011, 1021, tab.2, 3); Prusova & Smith, 2005 (p.76); Zuo & al., 2006 (p.162: tab.1); Isari & al., 2006 (p.241, tab.II); Lavaniegos & Jiménez-Pérez, 2006 (p.147, tab.2, 4, Rem.); Mackas & al., 2006 (L22S07, Table 2); Zervoudaki & al., 2006 (p.149, Table I); Hooff & Peterson, 2006 (p.2610); Koppelmann & Weikert, 2007 (p.266: tab.3); Alabaina & Irigoien, 2007 (p.435: Tab.1); Valdés & al., 2007 (p.103: tab.1); Cornils & al., 2007 (p.278, Table 2); 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.518); Fernandes, 2008 (p.465, Tabl.2); Gaard & al., 2008 (p.59, Table 1, N Mid-Atlantic Ridge); Ohtsuka & al., 2008 (p.115, Table 4); Raybaud & al., 2008 (p.1765, Table A1); Waggett & Buskey, 2008 (p.111, fig.2, Table 1); Galbraith, 2009 (pers. comm.); Miyashita & al., 2009 (p.815, Tabl.II); Labat & al., 2009 (p.1746, Table 2); Brugnano & al., 2010 (p.312, Table 3); Hafferssas & Seridji, 2010 (p.353, Table 2); Williamson & McGowan, 2010 (p.273, Table 3, Pacific central gyres: N and S); Cornils & al., 2010 (p.2076, Table 3); Schnack-Schiel & al., 2010 (p.2064, Table 2: E Atlantic subtropical/tropical); Hidalgo & al., 2010 (p.2089, Table 2); Mazzocchi & Di Capua, 2010 (p.424); Medellin-Mora & Navas S., 2010 (p.265, Tab. 2); Nowaczyk & al;, 2011 (p.2159, Table 2); Hsiao S.H. & al., 2011 (p.475, Appendix I); Shiganova & al., 2012 (p.61, Table 4); Uysal & Shmeleva, 2012 (p.909, Table I) | | | | NZ: | 22 | | | | | | | | | | | | | | | | | |  issued from : T.S.K. Björnberg in Bol. Inst. Oceanogr., Sao Paulo, 1963, XIII (1). [p.11, Fig.1].
Probability of occurrence of Calanus ( = Mesocalanus) tenuicornis in different environments.
T: Tropical waters (above 36.00 p.1000 salinity and above 20°C temperature); SST: Surface subtropical waters (salinity around 36 p.1000 and temperature 18°C or less); DST: Deeper shelf waters (salinity between 34 and 36, temperature under 20°C p.1000); SS: Surface shelf waters (same salinity and temperature above 20°C);
C: coastal waters with low salinity and variable temperature.
In each column no shading means no probability of finding the species in the samples from this environment; horizontal shading indicates the probability of finding the sepecies in percentages less than one in samples from this environment; cross shading indicates the probability of finding it in percentages higher than one and black shading represents the probability of finding it in the largest percentages of the total number of copepods.
Nota: For Björnberg, this species appeared only sparingly in the samples belonging to southern waters off Brazil with larger frequency in surface subtropical and in greater numbers in deeper shelf waters. It can be classified as an eurythermic cryophile prefering the lower end of the temperature range for warm waters. |
 issued from : G.A. Rebstock in Global change Biology, 2002, 8. [p.77, Fig.2 u].
Climatic regime shifts and decadal-scale variability in calanoid copepod populations off southern California (31°-35°N, 117°-122°W.
Cumulative sums of nonseasonal anomalies from the long-term means of copepod abundance from years 1950 to 2000.
A negative slope indicates a period of below-average anomalies; a positive slope indicates a period of above-average anomalies. Abrupt changes in slope indicate step changes.
The October 1966 cruise (prior to the increase in sampling depth), March 1976 cruise (prior to the 1976-77 climatic regime shift), and October 1988 cruise (prior to the hypothesized 1989 climatic regime shift) are marked with vertical lines. |
 issued from : A.A. Shmeleva in Bull. Inst. Oceanogr., Monaco, 1965, 65 (n°1351). [Table 6: 1]. As Calanus tenuicornis (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. |
| | | | Loc: | | | Cosmopolite: (sub-Antarct.: Pacif. SW, SE, sub-Arct.: rare), principalement tropical et tempéré): Afr. S (E & W), Atlant., Brazil, Caribbean Colombia, Caribbean Sea, Belize, Yucatan, G. du Mexique, off C. Hatteras, off E Cape Cod, off Nouvelle-Ecosse E, Flemish Cap, Mer du Nord, Canaries, Baie Ibéro-marocaine, off Coruña, G. de Gascogne, off Irlande N & SW, Médit. (Mer d'Alboran, Banyuls, Ligurian Sea, Tyrrhénienne, Strait of Messina, Adriatique, Ionienne, Mer Egée, Levantin Basin, Alexandrie, Black Sea), G. d'Aqaba, Mer Rouge, Mer Arabe, Natal, Madagascar, Rodrigues Is., Indian, Bay of Bengal, Indonésie-Malaisie, SW Celebes, Pacif. W (équatorial), mers de Chine (East Yellow Sea, China Sea, South China Sea), Taiwan, Kuroshio Current, Okinawa, Mer Jaune, Mer du Japon, Corée, Tsushima Straits, Japon (E, NE), off S Shikoku Is., off Hawaii N, G. d'Alaska (Columbia Bay), Colombie Britannique, Vancouver Is., Oregon (Yaquina, off Newport), California, Santa Monica Basin, W Baja California, G. de Californie, Pacific central gyres: N and S, Clipperton Is., W Costa Rica, Pérou, Chili (S, off Valparaiso), Pacif. S (NPFZ), Nouvelle-Zélande (Kaikoura, North Island SE) | | | | N: | 222 | | | | Lg.: | | | (22) F: 1,8; M: 1,8-1,5; (34) F: 1,84-1,78; (35) (N-Z) F: 2,1-1,8; (38) F: 2,18-2,12; (47) F: 2,5-1,9; M: 1,95-1,85; (72) F: 2,22-1,68; M: 1,88; (101) F: 1,87-1,68; M: 1,8; 1,56; (104) F: 2; (116) F: 2,32; M: 2,2; (125) F: 2,1-1,99; M: 1,77; (131) F: 2,05-1,54; M: 1,87-1,51; (142) F: 2-1,8; M: 1,8-1,5; (180) F: 2,06-1,65; M: 1,8-1,72; (187) F: 2,2-2,06; (196) F: 3,4-2; M: 1,9-1,7; (199) F: 2,13-1,52; M: 1,75-1,44; (237) F: 2,0; M: 1,85-1,6; (290) F: 2,05-2; M: 1,9-1,8; (327) M: 1,84; (330) F: 2,39-1,64; M: 2,02-1,71; (432) F: 2,5-2; (449) F: 2,5-1,9; M: 1,95-1,85; (786) F: 2,19-2,13; M: 2,12-1,81; (866) F: 1,5-2,2; M: 1,5-2; (920) F: 2,02 ± 0,017; (927) F: 2,05-2,08 (winter); 1,95-1,99 (Fall); (991) F: 1,8-2,5; M: 1,5-2,2; (1023) F: 1,76-1,89; M: 1,63-1,76; {F: 1,50-3,40; M: 1,50-2,20} | | | | Rem.: | épi à bathypélagique.
Sampling depth (sub-Antarct.) : 0-50 m.
Très nombreuses références , généralement sous la dénomination de Calanus tenuicornis , plus rarement Neocalanus tenuicornis.
Voir aussi les remarques en anglais | | | Dernière mise à jour : 15/05/2013 | |
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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 19 mai 2013] © copyright 2005-2012 CNRS, UPMC
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