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Fiche d'espèce de Copépode |
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Calanoida ( Ordre ) |
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Clausocalanoidea ( Superfamille ) |
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Scolecitrichidae ( Famille ) |
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Scolecithricella ( Genre ) |
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Scolecithricella tenuiserrata (Giesbrecht, 1892) (F,M) | |
| | | | | | | Syn.: | Scolecithrix tenuiserrata Giesbrecht, 1892 (p.266, 284, 775, figs.F,M); Giesbrecht & Schmeil, 1898 (p.43, Rem. F,M); Rose, 1924, p.5, 7, 8, 10); Bradford, 1973 (p.142); Bradford & al., 1983 (p.103); Brinton & al., 1986; Hure & Krsinic, 1998 (p.49, 101); Siokou-Frangou, 1999 (p.476);
No Amallothrix tenuiserrata (M) : Rose, 1942 (p.163, figs.M); ? Mazza, 1966 (p.71);
Amallothrix tenuiserrata : Mazzocchi & Di Capua, 2010 (p.427); in CalCOFI regional list (MDO, Nov. 2013; Belmonte, 2018 (p.273, Table I: Italian zones) M. Ohman, pers. comm.); Dias & al., 2019 (p.1, Table II, IV, fig.5, occurrrence, vertical distribution, Rem.: p.12) | | | | Ref.: | | | Farran, 1936 a (p.97, Rem.F); Sewell, 1947 (p.142); Grice, 1962 (p.208, figs.F,M, Rem.); Tanaka, 1962 (p.48, figs.M); Vervoort, 1965 (p.83, Rem.); Owre & Foyo, 1967 (p.61, figs.F,M); Corral Estrada, 1970 (p.163, figs.F,M, Rem.); Bowman, 1971 b (p.6); Greenwood, 1977 (p.58, fig.F); Carter, 1977 (p.35); Bradford & al., 1983 (p.103); Campaner, 1984 a (p.171, figs.F,M, Rem.); Bradford-Grieve & al., 1999 (p.881, 933, figs.F,M); Vyshkvartzeva, 1999 (2000) (p.234); Vives & Shmeleva, 2007 (p.787, figs.F,M, Rem.) |  issued from : O. Tanaka in Publ. Seto Mar. Biol. Lab., 1962, X (1). [p.49, Fig.133]. Male (from Sagami, in deep water): a, forehead (left lateral side); b, last thoracic segment and urosome (left lateral side); c, P1; d, P2; e, P3; f, P4; g, 5th pair of legs. Nota Male: - Posterolateral corners of the last thoracic segment rounded. - Abdomen 5-segmented. Abdominal segments and caudal rami proportional lengths 15 : 31 : 20 : 23 : 3 : 8 = 100. - Abdomen contained 2.65 times in the length of the cephalothorax. - 2nd abdominal segment longer than wide, the 3rd segment wider than long, the 4th as wide as long. - Caudal rami divergent, as wide as long. - A1 19-segmented, extends to the distal margin of the 1st abdominal segment. - A2 with exopod 1.4 times as long as the endopod. - Mx1 with 7+2 setae on outer lobe. - Mx2 has only vermiform filaments on the distal segments. - P1 without outer edge spine on the 1st exopodal segment. - P2 with the outer edge spine long and straight, as long as that on the exopodal 2nd segment; the middle spine on the outer margin of the 3rd segment is the longest; the terminal spine of the exopod has about 40 teeth; the outer margin of the coxa is indented; the inner margin of basis furnished with small spines on the middle. - P5 reaches back to the distal margin of the 3rd abdominal segment. Endopod of right leg very small; exopodal distal segment transformed into a short spine. Endopod of left leg short, extending about to the distal end of the 1st segment of the exopod of the same leg; exopod 3-segmented; the 2nd segment haired on the inner distal margin; the 3rd segment short, carries a small spine on the apex.
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 issued from : A.F. Campaner in Bolm. Zool., Univ. S. Paulo, 1984, 6 . [p.172, Fig.3]. Female (from off Rio de janeiro): a, habitus (dorsal); b, idem (lateral left side); b1, genital somite (lateral, enlarged); c, Md (cutting edge); d, Md (mandibular palp); e, Mx1; f, Mx2 (1-2: types of brush-like sensory setae; 3: variety ot type 1).
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 issued from : A.F. Campaner in Bolm. Zool., Univ. S. Paulo, 1984, 6 . [p.173, Fig.4]. Female: a, Mxp; b, P1 (posterior); c, P2 (posterior); d, P3 (posterior); d1, varieties of inner seta on basiodal segment 1 and endopodal segment 1 of P3; e, P4; f, P5.
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 issued from : A.F. Campaner in Bolm. Zool., Univ. S. Paulo, 1984, 6 . [p.174, Fig.5]. Male: a, habitus (dorsal); b, idem (lateral left side); b1, A1 (armature of segments 7-8); b2, right A1 (segment 16 of another specimen; c, Mx1 (inner lobe 1 removed); c1, Mx1 (inner lobe 1); d, Mx2 (endopodite); e, P2 (exopodite, posterior); f, P3 (exopodite, posterior); g, P5.
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 issued from : J. Corral Estrada in Tesis Doct., Univ. Madrid, A-129, Sec. Biologicas, 1970. [Lam.45, figs.1-7]. Male (from Canarias Is.): 1, habitus (dorsal); 2, P1; 3, P2; 4, P3; 5, P4; 6, P5. Female: 7, P5.
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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. Atlas von 54 Tafeln. [Taf.13, Fig.24]. As Scolecithrix tenuiserrata. Female: 24, P3 (posterior view).
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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. Atlas von 54 Tafeln. [Taf.13, Fig.39]. As Scolecithrix tenuiserrata. Female: P5.
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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. Atlas von 54 Tafeln. [Taf. 13 , Fig.16 ]. As Scolecithrix tenuiserrata. Female: 16, P4 (basipods only, posterior view).
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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. Atlas von 54 Tafeln. [Taf.13, Fig.25]. As Scolecithrix tenuiserrata. Male: P5 (posterior view).
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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. Atlas von 54 Tafeln. [Taf. 13 , Fig.16 ]. As Scolecithrix tenuiserrata. Female: 16, P4 (basipods only, posterior view).
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 issued from : G.D. Grice in Fish. Bull. Fish Wildl. Serv., 1962, 61. [p.209, Pl.17, Figs.9-21]. Female (from W equatorial Pacific): 9-10, habitus (dorsal and lateral, respectively); 11, rostrum; 12, A2; 13, Md; 14, Mx1; 15, terminal part of Mx2; 16, Mxp ( setae on endopod not shown); 17, P1; 18, P2 (setae not shown); 19, P3 (setae not shown); 20, P4 (setae not shown); 21, P5. Nota: Giesbrecht & Schmeil (1898) stated that the 2nd basal segment of Mx1 has 5 setae; the present specimens have 3 setae on this segment.
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 issued from : G.D. Grice in Fish. Bull. Fish Wildl. Serv., 1962, 61. [p.210, Pl.18, Fig.1]. Male: 1, P5. Nota: Although Giesbrecht & Schmeil indicated that the male is questionable, they gave the length as 1.45 mm as comparated to 1.15 mm for the female. The present males (1.0-1.27 mm) are also larger than the females (1.02-1.10 mm).
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 issued from : J.G. Greenwood in Proc. R. Soc. Qd, 1977, 88. [p.56, Fig.3, j]. Female (from 27°20'S, 153°15'E): j, P5.
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 issued from : H.B. Owre & M. Foyo in Fauna Caribaea, 1967, 1, Crustacea, 1: Copepoda. [p.60, Fig.384]. Male (from Florida Current): 384, P5. Nota: P5 long enogh to reach the distal margin of urosomal segment 3. Right endopod very small, less than one-third the length of exopod segment 1. left endopod almost the same length as exopodite 1; left exopod segment 2hirsute on the inner distal margin, and exopod segment 3 with a small spine at the apex.
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 issued from : O. Tanaka in Publ. Seto Mar. Biol. Lab., 1962, X (1). [p.49]. Male: Proportional lengths of segments of A1.
| | | | | Ref. compl.: | | | Sewell, 1948 (p.418, 502, 508, 521, 546); Moore, 1949 (p.50); Grice & Hulsemann, 1965 (p.224); Furuhashi, 1966 a (p.295, vertical distribution in Oyashio/Kuroshio transitional area, Table 8); Fleminger, 1967 a (tabl.1); Park, 1970 (p.476); Gamulin, 1971 (p.382, tab.3); Roe, 1972 (p.277, tabl.1, tabl.2); Binet & al., 1972 (p.53, 69); Apostolopoulou, 1972 (p.328, 351); Björnberg, 1973 (p.333, 389); Corral Estrada & Pereiro Muñoz, 1974 (tab.I); Carter, 1977 (1978) (p.35); Dessier, 1979 (p.205); Kovalev & Shmeleva, 1982 (p.84); Vives, 1982 (p.292); Dessier, 1983 (p.89, Tableau 1, Rem., %); Scotto di Carlo & al., 1984 (1044); Guangshan & Honglin, 1984 (p.118, tab.); Regner, 1985 (p.11, Rem.: p.32); Longhurst, 1985 (tab.2); Brinton & al., 1986 (p.228, Table 1); Madhupratap & Haridas, 1986 (p.105, tab.1); Rudyakov, 1986 (tab.1); Ambler & Miller, 1987 (tab.2, 3); Jimenez-Perez & Lara-Lara, 1988; Lozano Soldevilla & al., 1988 (p.59); Pancucci-Papadopoulou & al., 1990 (p.199); Suarez & al., 1990 (tab.2); Suarez, 1992 (App.1); Gopalakrishnan & Balachandran, 1992 (p.167, figs.1, 4, Table 1, 2); Shih & Young, 1995 (p.73); Gopalakrishnan & Saraledevi, 1998 (p.128, fig.3, chart); Suarez-Morales & Gasca, 1998 a (p.111); Madhupratap & al., 2001 (p. 1345, vertical distribution vs. O2, figs.4, 5: clusters, p.1353); Uysal al., 2002 (p.18, tab.1); Vukanic, 2003 (139, tab.1); Hsiao & al., 2004 (p.326, tab.1); Dur & al., 2007 (p.197, Table IV); Morales-Ramirez & Suarez-Morales, 2008 (p.522); Schnack-Schiel & al., 2010 (p.2064, Table 2: E Atlantic subtropical/tropical); Medellin-Mora & Navas S., 2010 (p.265, Tab. 2); Hsiao S.H. & al., 2011 (p.475, Appendix I); Maiphae & Sa-ardrit, 2011 (p.641, Table 2); Lidvanov & al., 2013 (p.290, Table 2, % composition); Bonecker & a., 2014 (p.445, Table II: frequency, horizontal & vertical distributions); Dias & al., 2015 (p.483, Table 2, abundance, biomass, production); Benedetti & al., 2016 (p.159, Table I, fig.1, functional characters); Benedetti & al., 2018 (p.1, Fig.2: ecological functional group); Belmonte, 2018 (p.273, Table I: Italian zones) | | | | NZ: | 15 | | |
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Carte de distribution de Scolecithricella tenuiserrata par zones géographiques
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| | | | | | | | | | | |  issued from : Gopalakrishnan & Saraledevi in Pelagic Biogeography ICoPB II. Proceedings of the 2nd International Conference. Final report of SCOR/IOC working group 93. Noordwijkerhout, The Netherlands 9-14 July 1995. Workshop Report No.142. UNESCO, 1998. [p.130, Fig.3].
Distribution and abundance in number of specimens/standard haul of Scolecithricella tenuiserrata in the Indian Ocean. |
 Issued from : C.O. Dias, A.V. de Araujo & S.L.C. Bonecker in An. Acad. Bras. Ciênc., 2019, 91 (1). [p.11, Fig.5, c]
Study area in The Campos basin (Brazil) showing the seasonal variation of Amallothrix tenuiserrata (= Scolecithricella tenuiserrata) (ind.m3) at 1 m depth, during the dry season.
Nota: This species was recorded only during the dry season and in greater abundance in the 1 m and 250 m depth levels, with reduced densities in the 2,000 m depth level. T.C. Gopalakrishna (unpubl. data) considered this species to be a strong migrant, undertaking nocturnal migrations in neritic and oceanic waters. The species inhabits intermediate depths up to the surface, and according to Gopalakrishna, in the Indian Ocean this species is most abundant in the highly saline upwelling waters of the Arabian Sea and warm tropical low saline surface waters of the Bay of Bengal (unpubl. data). The occurrence of the species only during the dry season in the Campos Basin can be related to unstable conditions due to the mobility of the tropical water-South Atlantic Central Water interface, an increase in which is associated with the highter temperatures of the ocean-atmosphere interface (see: Tsuchiya & al., 1994; Mémery & al., 2000). |
| | | | Loc: | | | South Africa (E), Congo, G. of Guinea, Ivorian coast, Canary Is., Morocco-Mauritania, NE Atlant. (? 30-60°N), S Brazil, off Rio de Janeiro, Campos Basin, off Amazon, Barbados Is., Caribbean Sea, Caribbean Colombia, G. of Mexico, Florida, Bermuda, Medit. (W Basin, Monaco, Ligurian Sea, Napoli, S Sicily, Ionian Sea, Adriatic Sea, Aegean Sea, Lebanon Basin), Arabian Sea, Natal, Indian, China Seas (East China Sea, South China Sea), Taiwan (SW & E), Japan, Pacif. (W equatorial), Australia (Great Barrier, Moreton Bay), Pacif. (equatorial), off NE Hawaii, E Pacif., California, Gulf of California, G. of Tehuantepec, off W Guatemala, W Costa Rica, off Chile (38°S) | | | | N: | 65 | | | | Lg.: | | | (16) F: 1,214-1,039; (34) F: 1,12-1; (47) F: 1,15; M: 1,45; (101) F: 1,1-1,02; M: 1,27-1; (117) M: 1,3; (180) F: 1,15; 1,11; M: 1,25; (199) F: 1,22-1,06; M: 1,37-1,29; (532) F: 1,15-1; M: 1,33-1,19; (920) F: 1,13; {F: 1,00-1,22; M: 1,00-1,45} | | | | Rem.: | épiplanctonique - ?.
Voir aussi les remarques en anglais | | | Dernière mise à jour : 09/12/2020 | |
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 Toute utilisation de ce site pour une publication sera mentionnée avec la référence suivante :
Razouls C., Desreumaux N., Kouwenberg J. et de Bovée F., 2005-2024. - Biodiversité des Copépodes planctoniques marins (morphologie, répartition géographique et données biologiques). Sorbonne Université, CNRS. Disponible sur http://copepodes.obs-banyuls.fr [Accédé le 21 novembre 2024] © copyright 2005-2024 Sorbonne Université, CNRS
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