Riscodopa Gordon 1989

Riscodopa Gordon, 1989 Type species : Riscodopa parva Gordon, 1989. Description Colony discoid, free living, budded radially, anchored by rhizoids originating from basal septular pores. Ancestrula either tatiform or similar to succeeding zooids. Zooid oriŽces with oral spines, paired lateral denticl...

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Main Authors: Cook, P. L., Bock, P. E.
Format: Text
Language:unknown
Published: Zenodo 2002
Subjects:
Online Access:https://dx.doi.org/10.5281/zenodo.5305765
https://zenodo.org/record/5305765
id ftdatacite:10.5281/zenodo.5305765
record_format openpolar
institution Open Polar
collection DataCite Metadata Store (German National Library of Science and Technology)
op_collection_id ftdatacite
language unknown
topic Biodiversity
Taxonomy
Animalia
Bryozoa
Gymnolaemata
Cheilostomatida
Petraliidae
Riscodopa
spellingShingle Biodiversity
Taxonomy
Animalia
Bryozoa
Gymnolaemata
Cheilostomatida
Petraliidae
Riscodopa
Cook, P. L.
Bock, P. E.
Riscodopa Gordon 1989
topic_facet Biodiversity
Taxonomy
Animalia
Bryozoa
Gymnolaemata
Cheilostomatida
Petraliidae
Riscodopa
description Riscodopa Gordon, 1989 Type species : Riscodopa parva Gordon, 1989. Description Colony discoid, free living, budded radially, anchored by rhizoids originating from basal septular pores. Ancestrula either tatiform or similar to succeeding zooids. Zooid oriŽces with oral spines, paired lateral denticles and a proximal lyrula. Avicularia lateral and oral, sometimes proximal and associated with a mucro. Ovicell hyperstomial, prominent, with numerous small pores or tubercles, known or inferred not to be closed by the operculum. Remarks Species here assigned to Riscodopa fall into two groups; the Recent species, which have a tatiform ancestrula, and the fossil species, which do not. Genera which include species with diVerent kinds of ancestrula have been documented (Cook, 1985: 51), and the genus Mucropetraliella , which is usually characterized by the presence of a proximal mucro and avicularium, does include some species in which these do not occur (Cook and Chimonides, 1981a: 117). Gordon (1989: 57) stipulated that there was ‘no suboral aviculiferous mucro’ in Riscodopa . A mucro occurs in R. biincisa and R. paucipora , but is absent from R. parva , R. cotyla and R. hyalina . However, the similarities in colony form and basal septular pores suggest that all the species described here may be contained within the genus Riscodopa . In all species, the ancestrula is surrounded by a circlet of Žve or six primary autozooids. These appear to be budded as a distal pair or triad, followed by a proximal triad, which may be derived equally from the lateral zooids as well as from the ancestrula. Riscodopa parva and R. cotyla live, anchored by basal rhizoids, on particulate substrata in deep water (477–4059 and 320–660 m, respectively), from the New Zealand shelf; R. hyalina occurs oV the coast of New South Wales from 429 to 503 m. The numerous other fossil bryozoan species associated with R. biincisa and R. paucipora in the Tertiary samples from Victoria suggest, in contrast, that although similar kinds of particulate sea-bottom occurred in Australian Tertiary seas, it is very unlikely that any of these fossil forms lived in deep water (Wass et al ., 1970). Similar apparent discrepancies between the known depth range of Recent species, and the depths inferred for their fossil congeners, occur among several groups of species in the Australian Tertiary, and have been noted for Selenariopsis (Bock and Cook, 1996), Siphonicytara (Bock and Cook, 2001) and for Chelidozoum and other species (Bock and Cook, in press). One possible explanation is that the hydrodynami c conditions of the shelf environments of the mid-Tertiary were much less agitated by wave activity than the modern shelf of southern Australia. This in turn, may be related to the narrower zone of open ocean that existed between Antarctica and Australia, or that the severe storms in this zone were less frequent or less intense during this interval of milder climate. The lack of strong bottom current or wave activity is also re ected in the presence of clay-rich sediments over large intervals and areas in the Tertiary, whereas clay-rich sediments are generally little-represented on the modern continental shelf. : Published as part of Cook, P. L. & Bock, P. E., 2002, Notes on astogeny of some Petraliellidae (Bryozoa) from Australia, pp. 1601-1619 in Journal of Natural History 36 (13) on page 1603, DOI: 10.1080/00222930110052463, http://zenodo.org/record/5298706 : {"references": ["GORDON, D. P., 1989, The marine fauna of New Zealand: Bryozoa: Gymnolaemata (Cheilostomida Ascophorina) from the western South Island continental shelf and slope, New Zealand Oceanographi c Institute Memoir, 97, 1 - 158.", "COOK, P. L. and CHIMONIDES, P. J., 1981 a, Morphology and systematics of some rooted cheilostome Bryozoa, Journal of Natural History, 15, 97 - 134.", "WASS, R. E., CONOLLY, J. R. and MACINTYRE, R. J., 1970, Bryozoan carbonate sand continuous along southern Australia, Marine Geology, 9, 63 - 73.", "BOCK, P. E. and COOK, P. L., 1996, The genus Selenariopsis Maplestone, 1913 (Bryozoa, Ascophorina), Records of the South Australian Museum, 29 (1), 23 - 31.", "BOCK, P. E. and COOK, P. L., 2001, A review of Australian Siphonicytara Busk (Bryozoa - Cheilostomatida), Records of the Western Australian Museum, 20, 307 - 322."]}
format Text
author Cook, P. L.
Bock, P. E.
author_facet Cook, P. L.
Bock, P. E.
author_sort Cook, P. L.
title Riscodopa Gordon 1989
title_short Riscodopa Gordon 1989
title_full Riscodopa Gordon 1989
title_fullStr Riscodopa Gordon 1989
title_full_unstemmed Riscodopa Gordon 1989
title_sort riscodopa gordon 1989
publisher Zenodo
publishDate 2002
url https://dx.doi.org/10.5281/zenodo.5305765
https://zenodo.org/record/5305765
geographic New Zealand
geographic_facet New Zealand
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
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spelling ftdatacite:10.5281/zenodo.5305765 2023-05-15T13:54:09+02:00 Riscodopa Gordon 1989 Cook, P. L. Bock, P. E. 2002 https://dx.doi.org/10.5281/zenodo.5305765 https://zenodo.org/record/5305765 unknown Zenodo http://zenodo.org/record/5298706 http://publication.plazi.org/id/FFE810125A47A05CE238D271FFD59023 https://zenodo.org/communities/biosyslit https://dx.doi.org/10.1080/00222930110052463 http://zenodo.org/record/5298706 http://publication.plazi.org/id/FFE810125A47A05CE238D271FFD59023 https://dx.doi.org/10.5281/zenodo.5305764 https://zenodo.org/communities/biosyslit Open Access Creative Commons Zero v1.0 Universal https://creativecommons.org/publicdomain/zero/1.0/legalcode cc0-1.0 info:eu-repo/semantics/openAccess CC0 Biodiversity Taxonomy Animalia Bryozoa Gymnolaemata Cheilostomatida Petraliidae Riscodopa article-journal ScholarlyArticle Text Taxonomic treatment 2002 ftdatacite https://doi.org/10.5281/zenodo.5305765 https://doi.org/10.1080/00222930110052463 https://doi.org/10.5281/zenodo.5305764 2022-03-10T15:47:48Z Riscodopa Gordon, 1989 Type species : Riscodopa parva Gordon, 1989. Description Colony discoid, free living, budded radially, anchored by rhizoids originating from basal septular pores. Ancestrula either tatiform or similar to succeeding zooids. Zooid oriŽces with oral spines, paired lateral denticles and a proximal lyrula. Avicularia lateral and oral, sometimes proximal and associated with a mucro. Ovicell hyperstomial, prominent, with numerous small pores or tubercles, known or inferred not to be closed by the operculum. Remarks Species here assigned to Riscodopa fall into two groups; the Recent species, which have a tatiform ancestrula, and the fossil species, which do not. Genera which include species with diVerent kinds of ancestrula have been documented (Cook, 1985: 51), and the genus Mucropetraliella , which is usually characterized by the presence of a proximal mucro and avicularium, does include some species in which these do not occur (Cook and Chimonides, 1981a: 117). Gordon (1989: 57) stipulated that there was ‘no suboral aviculiferous mucro’ in Riscodopa . A mucro occurs in R. biincisa and R. paucipora , but is absent from R. parva , R. cotyla and R. hyalina . However, the similarities in colony form and basal septular pores suggest that all the species described here may be contained within the genus Riscodopa . In all species, the ancestrula is surrounded by a circlet of Žve or six primary autozooids. These appear to be budded as a distal pair or triad, followed by a proximal triad, which may be derived equally from the lateral zooids as well as from the ancestrula. Riscodopa parva and R. cotyla live, anchored by basal rhizoids, on particulate substrata in deep water (477–4059 and 320–660 m, respectively), from the New Zealand shelf; R. hyalina occurs oV the coast of New South Wales from 429 to 503 m. The numerous other fossil bryozoan species associated with R. biincisa and R. paucipora in the Tertiary samples from Victoria suggest, in contrast, that although similar kinds of particulate sea-bottom occurred in Australian Tertiary seas, it is very unlikely that any of these fossil forms lived in deep water (Wass et al ., 1970). Similar apparent discrepancies between the known depth range of Recent species, and the depths inferred for their fossil congeners, occur among several groups of species in the Australian Tertiary, and have been noted for Selenariopsis (Bock and Cook, 1996), Siphonicytara (Bock and Cook, 2001) and for Chelidozoum and other species (Bock and Cook, in press). One possible explanation is that the hydrodynami c conditions of the shelf environments of the mid-Tertiary were much less agitated by wave activity than the modern shelf of southern Australia. This in turn, may be related to the narrower zone of open ocean that existed between Antarctica and Australia, or that the severe storms in this zone were less frequent or less intense during this interval of milder climate. The lack of strong bottom current or wave activity is also re ected in the presence of clay-rich sediments over large intervals and areas in the Tertiary, whereas clay-rich sediments are generally little-represented on the modern continental shelf. : Published as part of Cook, P. L. & Bock, P. E., 2002, Notes on astogeny of some Petraliellidae (Bryozoa) from Australia, pp. 1601-1619 in Journal of Natural History 36 (13) on page 1603, DOI: 10.1080/00222930110052463, http://zenodo.org/record/5298706 : {"references": ["GORDON, D. P., 1989, The marine fauna of New Zealand: Bryozoa: Gymnolaemata (Cheilostomida Ascophorina) from the western South Island continental shelf and slope, New Zealand Oceanographi c Institute Memoir, 97, 1 - 158.", "COOK, P. L. and CHIMONIDES, P. J., 1981 a, Morphology and systematics of some rooted cheilostome Bryozoa, Journal of Natural History, 15, 97 - 134.", "WASS, R. E., CONOLLY, J. R. and MACINTYRE, R. J., 1970, Bryozoan carbonate sand continuous along southern Australia, Marine Geology, 9, 63 - 73.", "BOCK, P. E. and COOK, P. L., 1996, The genus Selenariopsis Maplestone, 1913 (Bryozoa, Ascophorina), Records of the South Australian Museum, 29 (1), 23 - 31.", "BOCK, P. E. and COOK, P. L., 2001, A review of Australian Siphonicytara Busk (Bryozoa - Cheilostomatida), Records of the Western Australian Museum, 20, 307 - 322."]} Text Antarc* Antarctica DataCite Metadata Store (German National Library of Science and Technology) New Zealand