Beroe cucumis Fabricius 1780

BEROE CUCUMIS FABRICIUS, 1780 The body shape is strait or slightly oval in the oral part and oval at the aboral side, and it is more flattened in the paragastral plane than B. pseudocucumis (Fig. 6C, D). The adult length varies from 50 to 150 mm. Its length to width ratio (l/w) ranges 1.6–2.2. This...

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Main Authors: Shiganova, Tamara A., Abyzova, Galina A.
Format: Text
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Published: Zenodo 2021
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Online Access:https://dx.doi.org/10.5281/zenodo.5799226
https://zenodo.org/record/5799226
id ftdatacite:10.5281/zenodo.5799226
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
Ctenophora
Nuda
Beroida
Beroidae
Beroe
Beroe cucumis
spellingShingle Biodiversity
Taxonomy
Animalia
Ctenophora
Nuda
Beroida
Beroidae
Beroe
Beroe cucumis
Shiganova, Tamara A.
Abyzova, Galina A.
Beroe cucumis Fabricius 1780
topic_facet Biodiversity
Taxonomy
Animalia
Ctenophora
Nuda
Beroida
Beroidae
Beroe
Beroe cucumis
description BEROE CUCUMIS FABRICIUS, 1780 The body shape is strait or slightly oval in the oral part and oval at the aboral side, and it is more flattened in the paragastral plane than B. pseudocucumis (Fig. 6C, D). The adult length varies from 50 to 150 mm. Its length to width ratio (l/w) ranges 1.6–2.2. This ratio is variable: we observed specimens, which were shorter and longer, wider or slenderer, but never less than for B. pseudocucumis. Juvenile individuals may be narrower in the oral part of the body. Similar individuals were illustrated by Mayer (1912). The meridional canals lie under eight rows of ciliary combs, which extend about three-quarters of the distance from the aboral pole towards the mouth or a bit longer, but not up to the mouth. Its meridional canals have numerous diverticulae, which may branch out in adult ctenophores, but do not anastomose with each other, and do not connect with paragastral canals. At the aboral end, two oval polar-plates (Fig. 6A) surround the sense organ at the oval aboral pole, and are fringed with a row of short, branched papillae. Macrociliaries have three-toothed macrociliary tips with a somewhat larger middle tooth (Tamm & Tamm, 1993). Geographical distribution: Beroe cucumis was previously believed to be a widespread species, continuously distributed from the Arctic to the Antarctic (Pages & Orejas, 1999), but according to our genetic and morphological studies, and by comparison of published data, this species has a bipolar distribution, inhabiting cold polar and temperate waters, while being absent from tropical and subtropical zones. Distribution in the Arctic: all Eurasian seas (Sirenko, 2001), including the Barents Sea (Manko et al. , 2015; Bandara et al. , 2016; this study), the White Sea (Kosobokova & Pertsova, 2018), the Kara Sea (Dvoretsky & Dvoretsky, 2017), the Laptev Sea (Abramova & Tuschling, 2005), the East-Siberian Sea and the Chukchi Sea (Ershova et al. , 2015); Canada Basin (Raskoff et al. , 2005; Purcell et al. , 2010). Distribution in the Atlantic Ocean: individuals of Beroe cucumis were sampled from the North of Norway to the south-east of the North Sea and analysed genetically (this research). In the Atlantic Ocean Beroe cucumis individuals were sampled from the northern part of Norway to the south-east of the North Sea and analysed genetically (this research). Also, B. cucumis is known to occur in the northern and north-eastern Atlantic (Fabricius, 1780; Van Soest, 1973; Granhag et al. , 2012; Licandro et al. , 2015; Knutsen et al. , 2018), and along the eastern coasts of Canada and the USA (Mayer, 1912; Harbison et al. , 1978). In the Mediterranean Sea, and the subtropical, tropical and equatorial regions of the Atlantic Ocean, it is replaced by B. pseudocucumis . Additional genetic studies are required to clarify the boundaries of the B. cucumis occurrence off the coast of South America, but presumably B. cucumis occurs also in the temperate and subpolar waters of the South Atlantic and Antarctic (Siegel & Harm, 1996; Mianzan 1999; Mianzan & Guererro, 2000; Pakhomov et al. , 2000; Flores et al ., 2010, 2011). There is evidence of B. cucumis occurring in the Benguela Current near South Africa (Gibbons et al. , 1992). In the Pacific Ocean, Beroe cucumis occurs in cold waters: north-west Pacific (Kasuya et al. , 2000; Napazakov & Chuchukalo 2011); north-east Pacific, eastern Bering Sea (Hoff et al. , 2011); and the southeast Pacific off Chile (Pages & Orejas, 1999; Oliveira et al. , 2016). It frequently occurs in southern Australia (Stiasny, 1931; Edgar, 1997; Gershwin et al. , 2010) and in New Zealand waters (Ralph, 1950). Now that we have genetic confirmation of the presence of two species with a similar morphotype ( Beroe cucumis and B. pseudocucumis ), it is necessary to conduct a detailed analysis of the ecology and distribution of these two species. It is possible that there are areas of overlap in their habitat and geography. According to previous records, B. cucumis occurs in the areas between temperate and subtropical climatic zones, like the east coast of the USA (Mayer, 1912; Harbison et al. , 1978), the west coast of the USA (Wrobel & Mills, 1998) and the Yellow and East China seas (Liu, 2013; Yin et al. , 2017; Wang & Cheng, 2019). However, additional ecological and genetic studies of individuals in these areas are required to clarify the species identification and distribution. Habitat: Cold-water boreal species, has bipolar distribution and inhabits cold polar and temperate waters, while absent in tropical and subtropical zones. : Published as part of Shiganova, Tamara A. & Abyzova, Galina A., 2022, Revision of Beroidae (Ctenophora) in the southern seas of Europe: systematics and distribution based on genetics and morphology, pp. 297-322 in Zoological Journal of the Linnean Society 194 on page 308, DOI: 10.1093/zoolinnean/zlab021, http://zenodo.org/record/5799206 : {"references": ["Fabricius, O. 1780. Fauna Groenlandica. Copenhagen and Leipzig: J. G. Rothe, 450.", "Mayer AG. 1912. Ctenophores of the Atlantic coast of North America. Carnegie Institution of Washington Publication 162: 1 - 58.", "Tamm SL, Tamm S. 1993. Diversity of macrociliary size, tooth patterns, and distribution in Beroe (Ctenophora). Zoomorphology 113: 79 - 89.", "Pages F, Orejas C. 1999. Medusae, siphonophores and ctenophores of the Magellan region. Scientia Marina 63: 51 - 57.", "Sirenko BI. 2001. List of species of free-living invertebrates of Eurasian Arctic seas and adjacent deep waters. Moscow: Russian Academy of Science, Zoological Institute.", "Manko MK, Panasiuk-Chodnicka AA, Zmijewska MI. 2015. Pelagic coelenterates in the Atlantic sector of the Arctic Ocean-species diversity and distribution as water mass indicators. Oceanological and Hydrobiological Studies 44: 466 - 479.", "Bandara K, Varpe O, Soreide JE, Wallenschus J, Berge J, Eiane K. 2016. Seasonal vertical strategies in a high-Arctic coastal zooplankton community. Marine Ecology Progress Series 555: 49 - 64.", "Kosobokova KN, Pertsova NM. 2018. Zooplankton of the White Sea: communities, structure, seasonal dynamics, spatial distribution, and ecology. In: Lisitzin AP, Gordeev V, eds. Biogeochemistry of the atmosphere, ice and water of the White Sea. Cham: Springer, 223 - 266.", "Dvoretsky VG, Dvoretsky AG. 2017. Macrozooplankton of the Arctic - the Kara Sea in relation to environmental conditions. Estuarine, Coastal and Shelf Science 188: 38 - 55.", "Abramova E, Tuschling K. 2005. A 12 - year study of the seasonal and interannual dynamics of mesozooplankton in the Laptev Sea: significance of salinity regime and life cycle patterns. Global and Planetary Change 48: 141 - 164.", "Ershova EA, Hopcroft RR, Kosobokova KN. 2015. Interannual variability of summer mesozooplankton communities of the western Chukchi Sea: 2004 - 2012. Polar Biology 38: 1461 - 1481.", "Raskoff KA, Purcell JE, Hopcroft RR. 2005. Gelatinous zooplankton of the Arctic Ocean: in situ observations under the ice. Polar Biology 28: 207 - 217.", "Purcell JE, Hopcroft, RR, Kosobokova, KN, Whitledge TE. 2010. Distribution, abundance, and predation effects of epipelagic ctenophores and jellyfish in the western Arctic Ocean. Deep Sea Research Part II: Topical Studies in Oceanography 57: 127 - 135.", "Van Soest RWM. 1973. Planktonic coelenterates collected in the North Atlantic Ocean. Bijdragen tot de Dierkunde 43: 119 - 126.", "Granhag L, Majaneva S, Friis Moller L. 2012. First recordings of the ctenophore Euplokamis sp. (Ctenophora, Cydippida) in Swedish coastal waters and molecular identification of this genus. Aquatic Invasions 7: 455 - 463.", "Licandro P, Blackett M, Fischer A, Hosia A, Kennedy J, Kirby RR, Raab K, Stern R, Tranter P. 2015. Biogeography of jellyfish in the North Atlantic, by traditional and genomic methods. Earth System Science Data 7: 173 - 191.", "Knutsen T, Hosia A, Falkenhaug T, Skern-Mauritzen R, Wiebe PH, Larsen RB, Aglen A, Berg E. 2018. Coincident mass occurrence of gelatinous zooplankton in northern Norway. Frontiers in Marine Science 5: 158.", "Harbison GR, Madin LP, Swanberg NR. 1978. On the natural history and distribution of oceanic ctenophores. Deep Sea Research 25: 233 - 256.", "Siegel V, Harm U. 1996. The composition, abundance, biomass and diversity of the epipelagic zooplankton communities of the southern Bellingshausen Sea (Antarctic) with special references to krill and salps. Archive of Fishery and Marine Research 44: 115 - 139.", "Mianzan HW. 1999. Ctenophora. In: Boltovskoy D, ed. South Atlantic zooplankton. Leiden: Backhuys Publishers, 561 - 573.", "Mianzan HW, Guererro R. 2000. Environmental patterns and biomass distribution of gelatinous macrozooplankton. Three study cases in the southwestern Atlantic Ocean. Scientia Marina 64: 215 - 224.", "Pakhomov EA, Ansorge IJ, Froneman PW. 2000. Variability in the inter-island environment of the Prince Edward Islands (Southern Ocean). Polar Biology 23: 593 - 603.", "Flores H, Van Franeker JA, Feij B, Meijboom A, Van Dorssen M. 2010. Macrozooplankton and micronekton in the surface layer and under sea ice. In: Bathmann U, ed. The expedition of the research vessel ' Polarstern' to the Antarctic in 2007 / 2008 (ANT-XXIV / 2). Berichte zur Polar-und Meeresforschung (Reports on Polar and Marine Research). Bremerhaven, Germany: Alfred Wegener Institute, Helmholtz Centre for Polar and Marine Research (AWI), 604.", "Flores H, Van Franeker JA, Cisewski B, Leach H, Van de Putte AP, Meesters EH, Bathmann U, Wolff WJ. 2011. Macrofauna under sea ice and in the open surface layer of the Lazarev Sea, Southern Ocean. Deep Sea Research Part II: Topical Studies in Oceanography 58: 1948 - 1961.", "Gibbons MJ, Stuart V, Verheye HM. 1992. Tropic ecology of carnivorous zooplankton in the Benguela. South African Journal of Marine Science 12: 421 - 437.", "Kasuya T, Ishimaru T, Murano M. 2000. Seasonal variations in abundance and size composition of the lobate ctenophore Bolinopsis mikado (Moser) in Tokyo Bay, central Japan. Journal of Oceanography 56: 419 - 427.", "Napazakov VV, Chuchukalo VI. 2011. Feeding of Albatrossia pectoralis (Macrouridae) on the continental slope of eastern Kamchatka and the Kurils. Journal of Ichthyology 51: 343 - 351.", "Hoff GR, Britt LL. 2011. Results of the 2010 eastern Bering Sea upper continental slope survey of groundfish and invertebrate resources. US Department of Commerce, NOAA technical memorandum NMFS-AFSC- 224, 300.", "Oliveira OM, Miranda TP, Araujo EM, Ayon P, Cedeno- Posso CM, Cepeda-Mercado AA, Cordova P, Cunha AF, Genzano GN, Haddad MA, Mianzan HW. 2016. Census of Cnidaria (Medusozoa) and Ctenophora from South American marine waters. Zootaxa 4194: 1 - 256.", "Stiasny G. 1931. Uber einige coelenterata von Australien. Zoologische Mededelingen 14: 27 - 42.", "Edgar GJ. 1997. A new genus and three new species of Apseudomorph tanaidacean (Crustacea) from the Darwin region, 279 - 299, In: Hanly JR, Caswell G, Megirian D, Larson HK, eds. Proceedings of the Sixth International Marine Biological Workshop. The Marine Flora and Fauna of Darwin Harbour, Northern Territory, Australia. Darwin, Australia: Museums and Art Galleries of the Northern Territory and the Australian Marine Science Association.", "Gershwin, LA, Zeidler W, Davie PJ. 2010. Ctenophora of Australia. Memoirs of the Queensland Museum 54: 1 - 45.", "Ralph PM. 1950. Ctenophores from the waters of Cook Strait and Wellington Harbour. Transactions of the Royal Society of New Zealand 78: 70 - 82.", "Wrobel D, Mills C. 1998. Pacific coast pelagic invertebrates. A guide to the common gelatinous animals. Monterey: Sea Challengers & Monterey Bay Aquarium.", "Liu JY. 2013. Status of marine biodiversity of the China Seas. PLoS One 8: e 50719.", "Yin J, Zhang G, Li C, Wang S, Zhao Z, Wan A. 2017. Community composition, abundance and biomass of zooplankton in Zhangzi Island waters, northern Yellow Sea. Chinese Journal of Oceanology and Limnology 35: 1144 - 1151.", "Wang M, Cheng F. 2019. The complete mitochondrial genome of the Ctenophore Beroe cucumis, a mitochondrial genome showing rapid evolutionary rates. Mitochondrial DNA Part B 4: 3774 - 3775."]}
format Text
author Shiganova, Tamara A.
Abyzova, Galina A.
author_facet Shiganova, Tamara A.
Abyzova, Galina A.
author_sort Shiganova, Tamara A.
title Beroe cucumis Fabricius 1780
title_short Beroe cucumis Fabricius 1780
title_full Beroe cucumis Fabricius 1780
title_fullStr Beroe cucumis Fabricius 1780
title_full_unstemmed Beroe cucumis Fabricius 1780
title_sort beroe cucumis fabricius 1780
publisher Zenodo
publishDate 2021
url https://dx.doi.org/10.5281/zenodo.5799226
https://zenodo.org/record/5799226
long_lat ENVELOPE(12.917,12.917,-69.967,-69.967)
ENVELOPE(7.000,7.000,-68.000,-68.000)
ENVELOPE(166.000,166.000,74.000,74.000)
ENVELOPE(-57.467,-57.467,-63.267,-63.267)
ENVELOPE(-62.317,-62.317,-64.850,-64.850)
ENVELOPE(-79.150,-79.150,-73.483,-73.483)
ENVELOPE(11.100,11.100,64.609,64.609)
ENVELOPE(167.987,167.987,69.936,69.936)
ENVELOPE(-21.917,-21.917,-81.650,-81.650)
geographic Arctic
Antarctic
Southern Ocean
The Antarctic
Arctic Ocean
Barents Sea
Bering Sea
Laptev Sea
Kara Sea
Chukchi Sea
White Sea
Bellingshausen Sea
Canada
Pacific
Norway
New Zealand
Queensland
Lazarev
Lazarev Sea
East Siberian Sea
Mercado
Moser
Combs
Aglen
Ayon
Ershova
geographic_facet Arctic
Antarctic
Southern Ocean
The Antarctic
Arctic Ocean
Barents Sea
Bering Sea
Laptev Sea
Kara Sea
Chukchi Sea
White Sea
Bellingshausen Sea
Canada
Pacific
Norway
New Zealand
Queensland
Lazarev
Lazarev Sea
East Siberian Sea
Mercado
Moser
Combs
Aglen
Ayon
Ershova
genre Alfred Wegener Institute
Antarc*
Antarctic
Arctic
Arctic Ocean
Barents Sea
Bellingshausen Sea
Bering Sea
canada basin
Chukchi
Chukchi Sea
East Siberian Sea
Kamchatka
Kara Sea
laptev
Laptev Sea
Lazarev Sea
Mesozooplankton
North Atlantic
Northern Norway
Prince Edward Islands
Sea ice
Southern Ocean
White Sea
Zooplankton
genre_facet Alfred Wegener Institute
Antarc*
Antarctic
Arctic
Arctic Ocean
Barents Sea
Bellingshausen Sea
Bering Sea
canada basin
Chukchi
Chukchi Sea
East Siberian Sea
Kamchatka
Kara Sea
laptev
Laptev Sea
Lazarev Sea
Mesozooplankton
North Atlantic
Northern Norway
Prince Edward Islands
Sea ice
Southern Ocean
White Sea
Zooplankton
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spelling ftdatacite:10.5281/zenodo.5799226 2023-05-15T13:15:58+02:00 Beroe cucumis Fabricius 1780 Shiganova, Tamara A. Abyzova, Galina A. 2021 https://dx.doi.org/10.5281/zenodo.5799226 https://zenodo.org/record/5799226 unknown Zenodo http://zenodo.org/record/5799206 http://publication.plazi.org/id/FF9AF620FFADAB3F5F2B3B55270AB74E http://zoobank.org/A93B7D7A-1F8E-4E59-B86D-67814E01F797 https://zenodo.org/communities/biosyslit https://dx.doi.org/10.1093/zoolinnean/zlab021 http://zenodo.org/record/5799206 http://publication.plazi.org/id/FF9AF620FFADAB3F5F2B3B55270AB74E https://dx.doi.org/10.5281/zenodo.5799225 http://zoobank.org/A93B7D7A-1F8E-4E59-B86D-67814E01F797 https://dx.doi.org/10.5281/zenodo.5799227 https://zenodo.org/communities/biosyslit Open Access info:eu-repo/semantics/openAccess Biodiversity Taxonomy Animalia Ctenophora Nuda Beroida Beroidae Beroe Beroe cucumis Taxonomic treatment article-journal Text ScholarlyArticle 2021 ftdatacite https://doi.org/10.5281/zenodo.5799226 https://doi.org/10.1093/zoolinnean/zlab021 https://doi.org/10.5281/zenodo.5799225 https://doi.org/10.5281/zenodo.5799227 2022-02-08T18:12:30Z BEROE CUCUMIS FABRICIUS, 1780 The body shape is strait or slightly oval in the oral part and oval at the aboral side, and it is more flattened in the paragastral plane than B. pseudocucumis (Fig. 6C, D). The adult length varies from 50 to 150 mm. Its length to width ratio (l/w) ranges 1.6–2.2. This ratio is variable: we observed specimens, which were shorter and longer, wider or slenderer, but never less than for B. pseudocucumis. Juvenile individuals may be narrower in the oral part of the body. Similar individuals were illustrated by Mayer (1912). The meridional canals lie under eight rows of ciliary combs, which extend about three-quarters of the distance from the aboral pole towards the mouth or a bit longer, but not up to the mouth. Its meridional canals have numerous diverticulae, which may branch out in adult ctenophores, but do not anastomose with each other, and do not connect with paragastral canals. At the aboral end, two oval polar-plates (Fig. 6A) surround the sense organ at the oval aboral pole, and are fringed with a row of short, branched papillae. Macrociliaries have three-toothed macrociliary tips with a somewhat larger middle tooth (Tamm & Tamm, 1993). Geographical distribution: Beroe cucumis was previously believed to be a widespread species, continuously distributed from the Arctic to the Antarctic (Pages & Orejas, 1999), but according to our genetic and morphological studies, and by comparison of published data, this species has a bipolar distribution, inhabiting cold polar and temperate waters, while being absent from tropical and subtropical zones. Distribution in the Arctic: all Eurasian seas (Sirenko, 2001), including the Barents Sea (Manko et al. , 2015; Bandara et al. , 2016; this study), the White Sea (Kosobokova & Pertsova, 2018), the Kara Sea (Dvoretsky & Dvoretsky, 2017), the Laptev Sea (Abramova & Tuschling, 2005), the East-Siberian Sea and the Chukchi Sea (Ershova et al. , 2015); Canada Basin (Raskoff et al. , 2005; Purcell et al. , 2010). Distribution in the Atlantic Ocean: individuals of Beroe cucumis were sampled from the North of Norway to the south-east of the North Sea and analysed genetically (this research). In the Atlantic Ocean Beroe cucumis individuals were sampled from the northern part of Norway to the south-east of the North Sea and analysed genetically (this research). Also, B. cucumis is known to occur in the northern and north-eastern Atlantic (Fabricius, 1780; Van Soest, 1973; Granhag et al. , 2012; Licandro et al. , 2015; Knutsen et al. , 2018), and along the eastern coasts of Canada and the USA (Mayer, 1912; Harbison et al. , 1978). In the Mediterranean Sea, and the subtropical, tropical and equatorial regions of the Atlantic Ocean, it is replaced by B. pseudocucumis . Additional genetic studies are required to clarify the boundaries of the B. cucumis occurrence off the coast of South America, but presumably B. cucumis occurs also in the temperate and subpolar waters of the South Atlantic and Antarctic (Siegel & Harm, 1996; Mianzan 1999; Mianzan & Guererro, 2000; Pakhomov et al. , 2000; Flores et al ., 2010, 2011). There is evidence of B. cucumis occurring in the Benguela Current near South Africa (Gibbons et al. , 1992). In the Pacific Ocean, Beroe cucumis occurs in cold waters: north-west Pacific (Kasuya et al. , 2000; Napazakov & Chuchukalo 2011); north-east Pacific, eastern Bering Sea (Hoff et al. , 2011); and the southeast Pacific off Chile (Pages & Orejas, 1999; Oliveira et al. , 2016). It frequently occurs in southern Australia (Stiasny, 1931; Edgar, 1997; Gershwin et al. , 2010) and in New Zealand waters (Ralph, 1950). Now that we have genetic confirmation of the presence of two species with a similar morphotype ( Beroe cucumis and B. pseudocucumis ), it is necessary to conduct a detailed analysis of the ecology and distribution of these two species. It is possible that there are areas of overlap in their habitat and geography. According to previous records, B. cucumis occurs in the areas between temperate and subtropical climatic zones, like the east coast of the USA (Mayer, 1912; Harbison et al. , 1978), the west coast of the USA (Wrobel & Mills, 1998) and the Yellow and East China seas (Liu, 2013; Yin et al. , 2017; Wang & Cheng, 2019). However, additional ecological and genetic studies of individuals in these areas are required to clarify the species identification and distribution. Habitat: Cold-water boreal species, has bipolar distribution and inhabits cold polar and temperate waters, while absent in tropical and subtropical zones. : Published as part of Shiganova, Tamara A. & Abyzova, Galina A., 2022, Revision of Beroidae (Ctenophora) in the southern seas of Europe: systematics and distribution based on genetics and morphology, pp. 297-322 in Zoological Journal of the Linnean Society 194 on page 308, DOI: 10.1093/zoolinnean/zlab021, http://zenodo.org/record/5799206 : {"references": ["Fabricius, O. 1780. Fauna Groenlandica. Copenhagen and Leipzig: J. G. Rothe, 450.", "Mayer AG. 1912. Ctenophores of the Atlantic coast of North America. Carnegie Institution of Washington Publication 162: 1 - 58.", "Tamm SL, Tamm S. 1993. Diversity of macrociliary size, tooth patterns, and distribution in Beroe (Ctenophora). Zoomorphology 113: 79 - 89.", "Pages F, Orejas C. 1999. Medusae, siphonophores and ctenophores of the Magellan region. Scientia Marina 63: 51 - 57.", "Sirenko BI. 2001. List of species of free-living invertebrates of Eurasian Arctic seas and adjacent deep waters. Moscow: Russian Academy of Science, Zoological Institute.", "Manko MK, Panasiuk-Chodnicka AA, Zmijewska MI. 2015. Pelagic coelenterates in the Atlantic sector of the Arctic Ocean-species diversity and distribution as water mass indicators. Oceanological and Hydrobiological Studies 44: 466 - 479.", "Bandara K, Varpe O, Soreide JE, Wallenschus J, Berge J, Eiane K. 2016. Seasonal vertical strategies in a high-Arctic coastal zooplankton community. Marine Ecology Progress Series 555: 49 - 64.", "Kosobokova KN, Pertsova NM. 2018. Zooplankton of the White Sea: communities, structure, seasonal dynamics, spatial distribution, and ecology. In: Lisitzin AP, Gordeev V, eds. Biogeochemistry of the atmosphere, ice and water of the White Sea. Cham: Springer, 223 - 266.", "Dvoretsky VG, Dvoretsky AG. 2017. Macrozooplankton of the Arctic - the Kara Sea in relation to environmental conditions. Estuarine, Coastal and Shelf Science 188: 38 - 55.", "Abramova E, Tuschling K. 2005. A 12 - year study of the seasonal and interannual dynamics of mesozooplankton in the Laptev Sea: significance of salinity regime and life cycle patterns. Global and Planetary Change 48: 141 - 164.", "Ershova EA, Hopcroft RR, Kosobokova KN. 2015. Interannual variability of summer mesozooplankton communities of the western Chukchi Sea: 2004 - 2012. Polar Biology 38: 1461 - 1481.", "Raskoff KA, Purcell JE, Hopcroft RR. 2005. Gelatinous zooplankton of the Arctic Ocean: in situ observations under the ice. Polar Biology 28: 207 - 217.", "Purcell JE, Hopcroft, RR, Kosobokova, KN, Whitledge TE. 2010. Distribution, abundance, and predation effects of epipelagic ctenophores and jellyfish in the western Arctic Ocean. Deep Sea Research Part II: Topical Studies in Oceanography 57: 127 - 135.", "Van Soest RWM. 1973. Planktonic coelenterates collected in the North Atlantic Ocean. Bijdragen tot de Dierkunde 43: 119 - 126.", "Granhag L, Majaneva S, Friis Moller L. 2012. First recordings of the ctenophore Euplokamis sp. (Ctenophora, Cydippida) in Swedish coastal waters and molecular identification of this genus. Aquatic Invasions 7: 455 - 463.", "Licandro P, Blackett M, Fischer A, Hosia A, Kennedy J, Kirby RR, Raab K, Stern R, Tranter P. 2015. Biogeography of jellyfish in the North Atlantic, by traditional and genomic methods. Earth System Science Data 7: 173 - 191.", "Knutsen T, Hosia A, Falkenhaug T, Skern-Mauritzen R, Wiebe PH, Larsen RB, Aglen A, Berg E. 2018. Coincident mass occurrence of gelatinous zooplankton in northern Norway. Frontiers in Marine Science 5: 158.", "Harbison GR, Madin LP, Swanberg NR. 1978. On the natural history and distribution of oceanic ctenophores. Deep Sea Research 25: 233 - 256.", "Siegel V, Harm U. 1996. The composition, abundance, biomass and diversity of the epipelagic zooplankton communities of the southern Bellingshausen Sea (Antarctic) with special references to krill and salps. Archive of Fishery and Marine Research 44: 115 - 139.", "Mianzan HW. 1999. Ctenophora. In: Boltovskoy D, ed. South Atlantic zooplankton. Leiden: Backhuys Publishers, 561 - 573.", "Mianzan HW, Guererro R. 2000. Environmental patterns and biomass distribution of gelatinous macrozooplankton. Three study cases in the southwestern Atlantic Ocean. Scientia Marina 64: 215 - 224.", "Pakhomov EA, Ansorge IJ, Froneman PW. 2000. Variability in the inter-island environment of the Prince Edward Islands (Southern Ocean). Polar Biology 23: 593 - 603.", "Flores H, Van Franeker JA, Feij B, Meijboom A, Van Dorssen M. 2010. Macrozooplankton and micronekton in the surface layer and under sea ice. In: Bathmann U, ed. The expedition of the research vessel ' Polarstern' to the Antarctic in 2007 / 2008 (ANT-XXIV / 2). 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Mitochondrial DNA Part B 4: 3774 - 3775."]} Text Alfred Wegener Institute Antarc* Antarctic Arctic Arctic Ocean Barents Sea Bellingshausen Sea Bering Sea canada basin Chukchi Chukchi Sea East Siberian Sea Kamchatka Kara Sea laptev Laptev Sea Lazarev Sea Mesozooplankton North Atlantic Northern Norway Prince Edward Islands Sea ice Southern Ocean White Sea Zooplankton DataCite Metadata Store (German National Library of Science and Technology) Arctic Antarctic Southern Ocean The Antarctic Arctic Ocean Barents Sea Bering Sea Laptev Sea Kara Sea Chukchi Sea White Sea Bellingshausen Sea Canada Pacific Norway New Zealand Queensland Lazarev ENVELOPE(12.917,12.917,-69.967,-69.967) Lazarev Sea ENVELOPE(7.000,7.000,-68.000,-68.000) East Siberian Sea ENVELOPE(166.000,166.000,74.000,74.000) Mercado ENVELOPE(-57.467,-57.467,-63.267,-63.267) Moser ENVELOPE(-62.317,-62.317,-64.850,-64.850) Combs ENVELOPE(-79.150,-79.150,-73.483,-73.483) Aglen ENVELOPE(11.100,11.100,64.609,64.609) Ayon ENVELOPE(167.987,167.987,69.936,69.936) Ershova ENVELOPE(-21.917,-21.917,-81.650,-81.650)