@ARTICLE{TreeBASE2Ref25658,
author = {Janet M Bradford-Grieve and Leocadio Blanco-Bercial and Geoffrey A Boxshall},
title = {Revision of Family Megacalanidae (Copepoda: Calanoida)},
year = {2016},
keywords = {},
doi = {},
url = {http://},
pmid = {},
journal = {Zootaxa},
volume = {},
number = {},
pages = {},
abstract = {The Megacalanidae were revised based on new material collected during the CMarZ cruise XXIV/1 in the Atlantic Ocean and archived material loaned by Scripps Institution of Oceanography, Woods Hole Oceanographic Institution, Senckenberg Forschungsinstitut und Naturmuseum and the University of Hawaii. Distributional records were augmented from material held in the Smithsonian Institution, National Institute of Water and Atmospheric Research, Wellington, New Zealand, and the Museum of Natural History, London. Taxonomic confusion that has existed in the family is discussed and a method is suggested for stabilising names. A detailed examination of the morphology of this family, using the light microscope, has added further useful characters that distinguish genera and species. The added, hitherto undescribed, species include character states incompatible with aspects of previous generic definitions (e.g. presence or absence of setae on the maxillule coxal endite). Nevertheless, the cladistic and molecular analyses confimed that there are at least four monophyletic clades mostly with high bootstrap support. These clades represent already defined genera one of which [Elenacalanus nom. nov. (nomen novum)] replaces the preoccupied name Heterocalanus (Wolfenden, 1906). Four previously described species have been re-assigned to Elenacalanus in new combinations: E. princeps (Brady, 1883), E. eltaninae (Bj?rnberg, 1968), E. sverdrupi (Johnson, 1958) and E. inflatus (Bj?rnberg, 1968). Eleven new species are described: three Megacalanus, one Bradycalanus, six Bathycalanus, and one Elenacalanus. Bradycalanus enormis (Bj?rnberg, 1968) has been raised to species status based on genetic data although it can be only be distinguished from B. typicus by its large size. All four genera are diagnosed and keys are provided to the genera and species. We confirm that all male right antennules are geniculate in the Megacalanidae. Thirteen males are known. Of these males, eight are newly described (M. frosti n. sp., M. ericae n. sp., M. ohmani n. sp., Bathycalanus bradyi (Wolfenden, 1905), Ba. dentatus n. sp., Ba. milleri n. sp., Ba. unicornis Bj?rnberg, 1968, and Elenacalanus tageae n. sp.). We cannot be absolutely certain that the correct males have been assigned to the appropriate female so our decisions await testing with new data. The nauplius VI and copepodite II of M. princeps is described for the first time. The cladistic analysis provides the first morphology-based phylogeny. This scheme served as a working hypothesis which was tested and corroborated using the newly gathered molecular data. Vertical and horizontal distributions are summarised and the influence, if any, of environmental factors, and the evolutionary history, on observed distributions, is discussed. }
}
Citation for Study 19003
Citation title:
"Revision of Family Megacalanidae (Copepoda: Calanoida)".
Study name:
"Revision of Family Megacalanidae (Copepoda: Calanoida)".
This study is part of submission 19003
(Status: Published).
Citation
Bradford-grieve J.M., Blanco-bercial L., & Boxshall G.A. 2016. Revision of Family Megacalanidae (Copepoda: Calanoida). Zootaxa, .
Authors
-
Bradford-grieve J.M.
-
Blanco-bercial L.
-
Boxshall G.A.
Abstract
The Megacalanidae were revised based on new material collected during the CMarZ cruise XXIV/1 in the Atlantic Ocean and archived material loaned by Scripps Institution of Oceanography, Woods Hole Oceanographic Institution, Senckenberg Forschungsinstitut und Naturmuseum and the University of Hawaii. Distributional records were augmented from material held in the Smithsonian Institution, National Institute of Water and Atmospheric Research, Wellington, New Zealand, and the Museum of Natural History, London. Taxonomic confusion that has existed in the family is discussed and a method is suggested for stabilising names. A detailed examination of the morphology of this family, using the light microscope, has added further useful characters that distinguish genera and species. The added, hitherto undescribed, species include character states incompatible with aspects of previous generic definitions (e.g. presence or absence of setae on the maxillule coxal endite). Nevertheless, the cladistic and molecular analyses confimed that there are at least four monophyletic clades mostly with high bootstrap support. These clades represent already defined genera one of which [Elenacalanus nom. nov. (nomen novum)] replaces the preoccupied name Heterocalanus (Wolfenden, 1906). Four previously described species have been re-assigned to Elenacalanus in new combinations: E. princeps (Brady, 1883), E. eltaninae (Bj?rnberg, 1968), E. sverdrupi (Johnson, 1958) and E. inflatus (Bj?rnberg, 1968). Eleven new species are described: three Megacalanus, one Bradycalanus, six Bathycalanus, and one Elenacalanus. Bradycalanus enormis (Bj?rnberg, 1968) has been raised to species status based on genetic data although it can be only be distinguished from B. typicus by its large size. All four genera are diagnosed and keys are provided to the genera and species. We confirm that all male right antennules are geniculate in the Megacalanidae. Thirteen males are known. Of these males, eight are newly described (M. frosti n. sp., M. ericae n. sp., M. ohmani n. sp., Bathycalanus bradyi (Wolfenden, 1905), Ba. dentatus n. sp., Ba. milleri n. sp., Ba. unicornis Bj?rnberg, 1968, and Elenacalanus tageae n. sp.). We cannot be absolutely certain that the correct males have been assigned to the appropriate female so our decisions await testing with new data. The nauplius VI and copepodite II of M. princeps is described for the first time. The cladistic analysis provides the first morphology-based phylogeny. This scheme served as a working hypothesis which was tested and corroborated using the newly gathered molecular data. Vertical and horizontal distributions are summarised and the influence, if any, of environmental factors, and the evolutionary history, on observed distributions, is discussed.
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- Canonical resource URI:
http://purl.org/phylo/treebase/phylows/study/TB2:S19003
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@ARTICLE{TreeBASE2Ref25658,
author = {Janet M Bradford-Grieve and Leocadio Blanco-Bercial and Geoffrey A Boxshall},
title = {Revision of Family Megacalanidae (Copepoda: Calanoida)},
year = {2016},
keywords = {},
doi = {},
url = {http://},
pmid = {},
journal = {Zootaxa},
volume = {},
number = {},
pages = {},
abstract = {The Megacalanidae were revised based on new material collected during the CMarZ cruise XXIV/1 in the Atlantic Ocean and archived material loaned by Scripps Institution of Oceanography, Woods Hole Oceanographic Institution, Senckenberg Forschungsinstitut und Naturmuseum and the University of Hawaii. Distributional records were augmented from material held in the Smithsonian Institution, National Institute of Water and Atmospheric Research, Wellington, New Zealand, and the Museum of Natural History, London. Taxonomic confusion that has existed in the family is discussed and a method is suggested for stabilising names. A detailed examination of the morphology of this family, using the light microscope, has added further useful characters that distinguish genera and species. The added, hitherto undescribed, species include character states incompatible with aspects of previous generic definitions (e.g. presence or absence of setae on the maxillule coxal endite). Nevertheless, the cladistic and molecular analyses confimed that there are at least four monophyletic clades mostly with high bootstrap support. These clades represent already defined genera one of which [Elenacalanus nom. nov. (nomen novum)] replaces the preoccupied name Heterocalanus (Wolfenden, 1906). Four previously described species have been re-assigned to Elenacalanus in new combinations: E. princeps (Brady, 1883), E. eltaninae (Bj?rnberg, 1968), E. sverdrupi (Johnson, 1958) and E. inflatus (Bj?rnberg, 1968). Eleven new species are described: three Megacalanus, one Bradycalanus, six Bathycalanus, and one Elenacalanus. Bradycalanus enormis (Bj?rnberg, 1968) has been raised to species status based on genetic data although it can be only be distinguished from B. typicus by its large size. All four genera are diagnosed and keys are provided to the genera and species. We confirm that all male right antennules are geniculate in the Megacalanidae. Thirteen males are known. Of these males, eight are newly described (M. frosti n. sp., M. ericae n. sp., M. ohmani n. sp., Bathycalanus bradyi (Wolfenden, 1905), Ba. dentatus n. sp., Ba. milleri n. sp., Ba. unicornis Bj?rnberg, 1968, and Elenacalanus tageae n. sp.). We cannot be absolutely certain that the correct males have been assigned to the appropriate female so our decisions await testing with new data. The nauplius VI and copepodite II of M. princeps is described for the first time. The cladistic analysis provides the first morphology-based phylogeny. This scheme served as a working hypothesis which was tested and corroborated using the newly gathered molecular data. Vertical and horizontal distributions are summarised and the influence, if any, of environmental factors, and the evolutionary history, on observed distributions, is discussed. }
}
- Show RIS reference
TY - JOUR
ID - 25658
AU - Bradford-Grieve,Janet M
AU - Blanco-Bercial,Leocadio
AU - Boxshall,Geoffrey A
T1 - Revision of Family Megacalanidae (Copepoda: Calanoida)
PY - 2016
KW -
UR - http://dx.doi.org/
N2 - The Megacalanidae were revised based on new material collected during the CMarZ cruise XXIV/1 in the Atlantic Ocean and archived material loaned by Scripps Institution of Oceanography, Woods Hole Oceanographic Institution, Senckenberg Forschungsinstitut und Naturmuseum and the University of Hawaii. Distributional records were augmented from material held in the Smithsonian Institution, National Institute of Water and Atmospheric Research, Wellington, New Zealand, and the Museum of Natural History, London. Taxonomic confusion that has existed in the family is discussed and a method is suggested for stabilising names. A detailed examination of the morphology of this family, using the light microscope, has added further useful characters that distinguish genera and species. The added, hitherto undescribed, species include character states incompatible with aspects of previous generic definitions (e.g. presence or absence of setae on the maxillule coxal endite). Nevertheless, the cladistic and molecular analyses confimed that there are at least four monophyletic clades mostly with high bootstrap support. These clades represent already defined genera one of which [Elenacalanus nom. nov. (nomen novum)] replaces the preoccupied name Heterocalanus (Wolfenden, 1906). Four previously described species have been re-assigned to Elenacalanus in new combinations: E. princeps (Brady, 1883), E. eltaninae (Bj?rnberg, 1968), E. sverdrupi (Johnson, 1958) and E. inflatus (Bj?rnberg, 1968). Eleven new species are described: three Megacalanus, one Bradycalanus, six Bathycalanus, and one Elenacalanus. Bradycalanus enormis (Bj?rnberg, 1968) has been raised to species status based on genetic data although it can be only be distinguished from B. typicus by its large size. All four genera are diagnosed and keys are provided to the genera and species. We confirm that all male right antennules are geniculate in the Megacalanidae. Thirteen males are known. Of these males, eight are newly described (M. frosti n. sp., M. ericae n. sp., M. ohmani n. sp., Bathycalanus bradyi (Wolfenden, 1905), Ba. dentatus n. sp., Ba. milleri n. sp., Ba. unicornis Bj?rnberg, 1968, and Elenacalanus tageae n. sp.). We cannot be absolutely certain that the correct males have been assigned to the appropriate female so our decisions await testing with new data. The nauplius VI and copepodite II of M. princeps is described for the first time. The cladistic analysis provides the first morphology-based phylogeny. This scheme served as a working hypothesis which was tested and corroborated using the newly gathered molecular data. Vertical and horizontal distributions are summarised and the influence, if any, of environmental factors, and the evolutionary history, on observed distributions, is discussed.
L3 -
JF - Zootaxa
VL -
IS -
ER -