Isobactrus Newell 1947

Isobactrus Newell, 1947 (Figs 53 –60) Type species. Aletes setosus Lohmann, 1889. Adults. Female GP delicate and often in form of pair of crescentic plates on either side of GO, not or only slightly longer than GO and not distinctly delimited from striated integument. Female genital area with three...

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Main Author: Bartsch, Ilse
Format: Text
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Published: Zenodo 2015
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Online Access:https://dx.doi.org/10.5281/zenodo.5696485
https://zenodo.org/record/5696485
id ftdatacite:10.5281/zenodo.5696485
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
Arthropoda
Arachnida
Trombidiformes
Halacaridae
Isobactrus
spellingShingle Biodiversity
Taxonomy
Animalia
Arthropoda
Arachnida
Trombidiformes
Halacaridae
Isobactrus
Bartsch, Ilse
Isobactrus Newell 1947
topic_facet Biodiversity
Taxonomy
Animalia
Arthropoda
Arachnida
Trombidiformes
Halacaridae
Isobactrus
description Isobactrus Newell, 1947 (Figs 53 –60) Type species. Aletes setosus Lohmann, 1889. Adults. Female GP delicate and often in form of pair of crescentic plates on either side of GO, not or only slightly longer than GO and not distinctly delimited from striated integument. Female genital area with three (rarely four) pairs of pgs, anterior pair in striated integument, anterior to GO, following two pairs level with and posterior to GO, respectively, in margin or outside GP. Anterior and posterior edge of genital foramen often enforced by internal pregenital and postgenital sclerites (Fig. 53). Genital sclerites with one to two pairs of sgs. Female with two or three almost equal-sized internal tube-like gac (Figs 54, 56), or two pairs of distinct, tube-like and one pair of small gac (Fig. 53; Viets 1939 b: fig. 21; Newell 1947: figs 55, 80; Bartsch 1974 b: fig. 2 b; Abé 1996 a: figs 4 A, 8 A, 16 A, 20 A, 1996 b: fig. 2 A) (the posterior markings illustrated in Newell 1947: fig. 59 are no acetabula). Ovipositor short, both at rest and when everted. Genital spines well-sclerotized, rather wide and palmate, generally ending with several tines; 10–11 spines present, four in anterior and six to seven in posterior position (Bartsch 1975 a: figs 10 b, 11, 1975 b: fig 103, 2000: fig. 1 D; Newell 1984: fig. 42). GP in male larger than in female, with about 30–100 perigenital setae, these often arranged in an inner and outer ring around GO and inserted on GP, rarely in striated integument outside GP. Setae generally slender and smooth, in a few species some of anterior setae of inner ring short, bristle-like or spiniform, namely in I. hutchinsoni Newell, 1947 and I. uniscutatus (Viets, 1939) (Fig. 60; Newell 1947: fig. 76). Genital sclerites with four (rarely three) pairs of sgs, these setiform, rarely flattened and foliate or spur-like. Acetabula generally slightly smaller than in females and situated in posterior part of GO or even posterior to GO (Fig. 60). As in female, male GO with either two to three pairs of large almost equal-sized gac or two large pairs and one anterior small pair (Fig. 56; Viets 1939 b: fig. 21; Newell 1947: fig. 76, 1984: fig. 37; Abé 1996 a: figs 4 B, 16 B; 1996 b: fig. 2 B; Bartsch 2003 a: fig. 2 M). Acetabula generally internal, in two species ( I. hutchinsoni , I . uniscutatus ) two pairs of external acetabula present (Newell 1947: fig. 76; Bartsch 1979 b: fig. 13, 2003 c: fig. 3 F). Juveniles. With four juvenile stages, one larva and three nymphs (proto-, deuto-, tritonymph). Nymphal genital and anal plate in some species separated in others fused. Tritonymph with a pair of small sgs and two pairs of pgs, one pair in striated integument anterior to GP, one pair on or close to GP. Genital region with two or three pairs of almost equal-sized acetabula (Fig. 55, 57; Newell 1947: fig. 81; Bartsch 1972: fig. 18 G, 2005 c: fig. 14, 2009 b: figs 5 F, 7 G; Abé 1996 b: fig. 2 C) or with pair of large anterior acetabula, small, short middle pair, more or less adjacent to anterior pair of gac, and slender posterior pair (Bartsch 1972: fig. 21 D, 1975 b: figs 81, 100, 121; Abé 1996 a: figs 16 C, 23 A). Deuto- and protonymph without sgs. Deutonymph with single pair of pgs situated level with gac and on or in margin of GP. Majority of deutonymphs with two pairs of gac, either equal-sized (Abé 1996 b: Fig. 2 D) or with small anterior and large posterior pair of gac (Bartsch 1972: fig. 21 C, 1975 b: figs 82, 101, 120; Abé 1996 a: figs 4 C, 23 B), or with single pair of gac (Fig. 58; Newell 1947: p. 80; Bartsch 1972: p. 191, fig. 18 D). Protonymph with single pair of internal gac; pgs and sgs lacking (Fig. 59; Bartsch 1972: fig. 21 B, 1975 b: figs 83, 102, 119; Abé 1996 a: fig. 23 C, 1996 b: fig. 2 E). Larva with pair of epimeral pores (Bartsch 1974 b: fig. 1 a, 2 c). Remarks. At present 29 species are known. The species live in a zone more or less regularly emerged; all feed on algae. The genus is spread world-wide but three different lineages have been separated on the basis of their character combinations (Abé 2001; Bartsch 2010 a). The species of each lineage are concentrated within a geographical area which roughly can be attributed to the temperate northern Atlantic and Pacific Ocean (ca 75 °N to 25 °N), the tropics (ca 25 °N to 25 °S) and the temperate southern Pacific and Indian Ocean (ca 25 °S to 55 °S). The different number and shape of the genital acetabula are in concordance with these three groups. Adults and tritonymphs from the southern temperate zone have two pairs of acetabula, those from the tropics three pairs, and those from the northern temperate zone generally two pairs of large-sized and one pair of small acetabula. Exceptions are the North Atlantic species I . uniscutatus and I. hutchinsoni which have two pairs of acetabula; populations of both can survive in low saline brackish water. The deutonymphs of the southern temperate zone have a single pair of gac, those from the tropics two equal-sized pairs and species from the northern temperate zone a large and a minute pair of acetabula, again with the exception of I . uniscutatus which bears a single pair of acetabula. : Published as part of Bartsch, Ilse, 2015, The genital area of Halacaridae (Acari), life stages and development of morphological characters and implication on the classification, pp. 201-259 in Zootaxa 3919 (2) on pages 220-222, DOI: 10.11646/zootaxa.3919.2.1, http://zenodo.org/record/245246 : {"references": ["Newell, I. M. (1947) A systematic and ecological study of the Halacaridae of eastern North America. Bulletin of the Bingham Oceanographic Collection, 10, 1 - 232.", "Lohmann, H. (1889) Die Unterfamilie der Halacaridae Murr. und die Meeresmilben der Ostsee. Zoologische Jahrbucher, Abteilung fur Systematik, Okologie und Geographie der Tiere, 4, 269 - 408.", "Viets, K. (1939 b) Meeresmilben aus der Adria (Halacaridae und Hydrachnellae, Acari). Archiv fur Naturgeschichte, (Neue Folge) 8, 518 - 550.", "Bartsch, I. (1974 b) Uber das Auftreten von Epimeralporen besonders bei den Rhombognathinae (Halacaridae, Acari). Zoologischer Anzeiger, 193, 266 - 268.", "Abe, H. (1996 a) Rhombognathine mites (Acari: Halacaridae) from Hokkaido, Northern Japan. Publications of the Seto Marine Biological Laboratory, 37, 63 - 166.", "Bartsch, I. (1975 a) Ein Beitrag zum System der Rhombognathinen (Halacaridae, Acari). Zur Morphologie der Tarsalregion und des Ovipositors. Zoologischer Anzeiger, 194, 193 - 200.", "Newell, I. M. (1984) Antarctic Halacaroidea. Antarctic Research Series, 40, 1 - 284. http: // dx. doi. org / 10.1029 / AR 040", "Bartsch, I. (2003 a) Mangrove halacarid fauna (Halacaridae, Acari) of the Dampier region, Western Australia, with description of five new species. Journal of Natural History, 37, 1855 - 1877. http: // dx. doi. org / 10.1080 / 00222930110089184", "Bartsch, I. (1979 b) Halacaridae (Acari) von der Atlantikkuste Nordamerikas. Beschreibung der Arten. Mikrofauna des Meeresbodens, 79, 1 - 62.", "Bartsch, I. (1972) Ein Beitrag zur Systematik, Biologie und Okologie der Halacaridae (Acari) aus dem Litoral der Nord- und Ostsee. I. Systematik und Biologie. Abhandlungen und Verhandlungen des Naturwissenschaftlichen Vereins zu Hamburg, Neue Folge, 16, 155 - 230.", "Abe, H. (1996 b) A new species of the genus Isobactrus (Acari: Halacaridae) from Ponape, Micronesia, with special reference to intrageneric character state distribution. Species Diversity, 1, 17 - 29.", "Abe, H. (2001) Phylogeny and character evolution of the marine genus Isobactrus (Acari: Halacaridae). Journal of Natural History, 35, 617 - 625. http: // dx. doi. org / 10.1080 / 00222930151098279", "Bartsch, I. (2010 a) Reflections on distribution and origin of the halacarid genus Isobactrus (Acari: Halacaridae). Marine Biodiversity, 40, 17 - 32. http: // dx. doi. org / 10.1007 / s 12526 - 009 - 0030 - 7"]}
format Text
author Bartsch, Ilse
author_facet Bartsch, Ilse
author_sort Bartsch, Ilse
title Isobactrus Newell 1947
title_short Isobactrus Newell 1947
title_full Isobactrus Newell 1947
title_fullStr Isobactrus Newell 1947
title_full_unstemmed Isobactrus Newell 1947
title_sort isobactrus newell 1947
publisher Zenodo
publishDate 2015
url https://dx.doi.org/10.5281/zenodo.5696485
https://zenodo.org/record/5696485
long_lat ENVELOPE(-63.400,-63.400,-69.400,-69.400)
ENVELOPE(-59.533,-59.533,-62.333,-62.333)
geographic Antarctic
Pacific
Indian
Bingham
Newell
geographic_facet Antarctic
Pacific
Indian
Bingham
Newell
genre Antarc*
Antarctic
North Atlantic
genre_facet Antarc*
Antarctic
North Atlantic
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spelling ftdatacite:10.5281/zenodo.5696485 2023-05-15T13:59:05+02:00 Isobactrus Newell 1947 Bartsch, Ilse 2015 https://dx.doi.org/10.5281/zenodo.5696485 https://zenodo.org/record/5696485 unknown Zenodo http://zenodo.org/record/245246 http://publication.plazi.org/id/FFF1FF9DFFEBFF92FF85A71FFFE8FF86 http://zoobank.org/8CB77F9E-A35E-43E2-91F7-7822AE421B33 https://zenodo.org/communities/biosyslit https://dx.doi.org/10.11646/zootaxa.3919.2.1 http://zenodo.org/record/245246 http://publication.plazi.org/id/FFF1FF9DFFEBFF92FF85A71FFFE8FF86 https://dx.doi.org/10.5281/zenodo.245251 https://dx.doi.org/10.5281/zenodo.245247 http://zoobank.org/8CB77F9E-A35E-43E2-91F7-7822AE421B33 https://dx.doi.org/10.5281/zenodo.5696486 https://zenodo.org/communities/biosyslit Open Access info:eu-repo/semantics/openAccess Biodiversity Taxonomy Animalia Arthropoda Arachnida Trombidiformes Halacaridae Isobactrus Taxonomic treatment article-journal Text ScholarlyArticle 2015 ftdatacite https://doi.org/10.5281/zenodo.5696485 https://doi.org/10.11646/zootaxa.3919.2.1 https://doi.org/10.5281/zenodo.245251 https://doi.org/10.5281/zenodo.245247 https://doi.org/10.5281/zenodo.5696486 2022-02-08T13:42:09Z Isobactrus Newell, 1947 (Figs 53 –60) Type species. Aletes setosus Lohmann, 1889. Adults. Female GP delicate and often in form of pair of crescentic plates on either side of GO, not or only slightly longer than GO and not distinctly delimited from striated integument. Female genital area with three (rarely four) pairs of pgs, anterior pair in striated integument, anterior to GO, following two pairs level with and posterior to GO, respectively, in margin or outside GP. Anterior and posterior edge of genital foramen often enforced by internal pregenital and postgenital sclerites (Fig. 53). Genital sclerites with one to two pairs of sgs. Female with two or three almost equal-sized internal tube-like gac (Figs 54, 56), or two pairs of distinct, tube-like and one pair of small gac (Fig. 53; Viets 1939 b: fig. 21; Newell 1947: figs 55, 80; Bartsch 1974 b: fig. 2 b; Abé 1996 a: figs 4 A, 8 A, 16 A, 20 A, 1996 b: fig. 2 A) (the posterior markings illustrated in Newell 1947: fig. 59 are no acetabula). Ovipositor short, both at rest and when everted. Genital spines well-sclerotized, rather wide and palmate, generally ending with several tines; 10–11 spines present, four in anterior and six to seven in posterior position (Bartsch 1975 a: figs 10 b, 11, 1975 b: fig 103, 2000: fig. 1 D; Newell 1984: fig. 42). GP in male larger than in female, with about 30–100 perigenital setae, these often arranged in an inner and outer ring around GO and inserted on GP, rarely in striated integument outside GP. Setae generally slender and smooth, in a few species some of anterior setae of inner ring short, bristle-like or spiniform, namely in I. hutchinsoni Newell, 1947 and I. uniscutatus (Viets, 1939) (Fig. 60; Newell 1947: fig. 76). Genital sclerites with four (rarely three) pairs of sgs, these setiform, rarely flattened and foliate or spur-like. Acetabula generally slightly smaller than in females and situated in posterior part of GO or even posterior to GO (Fig. 60). As in female, male GO with either two to three pairs of large almost equal-sized gac or two large pairs and one anterior small pair (Fig. 56; Viets 1939 b: fig. 21; Newell 1947: fig. 76, 1984: fig. 37; Abé 1996 a: figs 4 B, 16 B; 1996 b: fig. 2 B; Bartsch 2003 a: fig. 2 M). Acetabula generally internal, in two species ( I. hutchinsoni , I . uniscutatus ) two pairs of external acetabula present (Newell 1947: fig. 76; Bartsch 1979 b: fig. 13, 2003 c: fig. 3 F). Juveniles. With four juvenile stages, one larva and three nymphs (proto-, deuto-, tritonymph). Nymphal genital and anal plate in some species separated in others fused. Tritonymph with a pair of small sgs and two pairs of pgs, one pair in striated integument anterior to GP, one pair on or close to GP. Genital region with two or three pairs of almost equal-sized acetabula (Fig. 55, 57; Newell 1947: fig. 81; Bartsch 1972: fig. 18 G, 2005 c: fig. 14, 2009 b: figs 5 F, 7 G; Abé 1996 b: fig. 2 C) or with pair of large anterior acetabula, small, short middle pair, more or less adjacent to anterior pair of gac, and slender posterior pair (Bartsch 1972: fig. 21 D, 1975 b: figs 81, 100, 121; Abé 1996 a: figs 16 C, 23 A). Deuto- and protonymph without sgs. Deutonymph with single pair of pgs situated level with gac and on or in margin of GP. Majority of deutonymphs with two pairs of gac, either equal-sized (Abé 1996 b: Fig. 2 D) or with small anterior and large posterior pair of gac (Bartsch 1972: fig. 21 C, 1975 b: figs 82, 101, 120; Abé 1996 a: figs 4 C, 23 B), or with single pair of gac (Fig. 58; Newell 1947: p. 80; Bartsch 1972: p. 191, fig. 18 D). Protonymph with single pair of internal gac; pgs and sgs lacking (Fig. 59; Bartsch 1972: fig. 21 B, 1975 b: figs 83, 102, 119; Abé 1996 a: fig. 23 C, 1996 b: fig. 2 E). Larva with pair of epimeral pores (Bartsch 1974 b: fig. 1 a, 2 c). Remarks. At present 29 species are known. The species live in a zone more or less regularly emerged; all feed on algae. The genus is spread world-wide but three different lineages have been separated on the basis of their character combinations (Abé 2001; Bartsch 2010 a). The species of each lineage are concentrated within a geographical area which roughly can be attributed to the temperate northern Atlantic and Pacific Ocean (ca 75 °N to 25 °N), the tropics (ca 25 °N to 25 °S) and the temperate southern Pacific and Indian Ocean (ca 25 °S to 55 °S). The different number and shape of the genital acetabula are in concordance with these three groups. Adults and tritonymphs from the southern temperate zone have two pairs of acetabula, those from the tropics three pairs, and those from the northern temperate zone generally two pairs of large-sized and one pair of small acetabula. Exceptions are the North Atlantic species I . uniscutatus and I. hutchinsoni which have two pairs of acetabula; populations of both can survive in low saline brackish water. The deutonymphs of the southern temperate zone have a single pair of gac, those from the tropics two equal-sized pairs and species from the northern temperate zone a large and a minute pair of acetabula, again with the exception of I . uniscutatus which bears a single pair of acetabula. : Published as part of Bartsch, Ilse, 2015, The genital area of Halacaridae (Acari), life stages and development of morphological characters and implication on the classification, pp. 201-259 in Zootaxa 3919 (2) on pages 220-222, DOI: 10.11646/zootaxa.3919.2.1, http://zenodo.org/record/245246 : {"references": ["Newell, I. M. (1947) A systematic and ecological study of the Halacaridae of eastern North America. Bulletin of the Bingham Oceanographic Collection, 10, 1 - 232.", "Lohmann, H. (1889) Die Unterfamilie der Halacaridae Murr. und die Meeresmilben der Ostsee. Zoologische Jahrbucher, Abteilung fur Systematik, Okologie und Geographie der Tiere, 4, 269 - 408.", "Viets, K. (1939 b) Meeresmilben aus der Adria (Halacaridae und Hydrachnellae, Acari). Archiv fur Naturgeschichte, (Neue Folge) 8, 518 - 550.", "Bartsch, I. (1974 b) Uber das Auftreten von Epimeralporen besonders bei den Rhombognathinae (Halacaridae, Acari). Zoologischer Anzeiger, 193, 266 - 268.", "Abe, H. (1996 a) Rhombognathine mites (Acari: Halacaridae) from Hokkaido, Northern Japan. Publications of the Seto Marine Biological Laboratory, 37, 63 - 166.", "Bartsch, I. (1975 a) Ein Beitrag zum System der Rhombognathinen (Halacaridae, Acari). Zur Morphologie der Tarsalregion und des Ovipositors. Zoologischer Anzeiger, 194, 193 - 200.", "Newell, I. M. (1984) Antarctic Halacaroidea. Antarctic Research Series, 40, 1 - 284. http: // dx. doi. org / 10.1029 / AR 040", "Bartsch, I. (2003 a) Mangrove halacarid fauna (Halacaridae, Acari) of the Dampier region, Western Australia, with description of five new species. Journal of Natural History, 37, 1855 - 1877. http: // dx. doi. org / 10.1080 / 00222930110089184", "Bartsch, I. (1979 b) Halacaridae (Acari) von der Atlantikkuste Nordamerikas. Beschreibung der Arten. Mikrofauna des Meeresbodens, 79, 1 - 62.", "Bartsch, I. (1972) Ein Beitrag zur Systematik, Biologie und Okologie der Halacaridae (Acari) aus dem Litoral der Nord- und Ostsee. I. Systematik und Biologie. Abhandlungen und Verhandlungen des Naturwissenschaftlichen Vereins zu Hamburg, Neue Folge, 16, 155 - 230.", "Abe, H. (1996 b) A new species of the genus Isobactrus (Acari: Halacaridae) from Ponape, Micronesia, with special reference to intrageneric character state distribution. Species Diversity, 1, 17 - 29.", "Abe, H. (2001) Phylogeny and character evolution of the marine genus Isobactrus (Acari: Halacaridae). Journal of Natural History, 35, 617 - 625. http: // dx. doi. org / 10.1080 / 00222930151098279", "Bartsch, I. (2010 a) Reflections on distribution and origin of the halacarid genus Isobactrus (Acari: Halacaridae). Marine Biodiversity, 40, 17 - 32. http: // dx. doi. org / 10.1007 / s 12526 - 009 - 0030 - 7"]} Text Antarc* Antarctic North Atlantic DataCite Metadata Store (German National Library of Science and Technology) Antarctic Pacific Indian Bingham ENVELOPE(-63.400,-63.400,-69.400,-69.400) Newell ENVELOPE(-59.533,-59.533,-62.333,-62.333)