Diplodinium cameli subsp. f var. bispinatum Kubesy & Dehority, 2002, f. n.

Diplodinium cameli f. bispinatum f. n. (Figs. 4­6) With all the characteristics of the species. Single spines arise from both the dorsal and ventral sides approximately five­sixths of the cell length towards the posterior end. The dorsal spine is well developed in most cells, averaging around 12 m,...

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Main Authors: Kubesy, A. A., Dehority, Burk A.
Format: Text
Language:unknown
Published: Zenodo 2002
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Online Access:https://dx.doi.org/10.5281/zenodo.5586600
https://zenodo.org/record/5586600
id ftdatacite:10.5281/zenodo.5586600
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
Protozoa
Ciliophora
Kinetofragminophora
Trichostomatida
Blepharocorythidae
Diplodinium
Diplodinium cameli
Diplodinium cameli f. bispinatum
spellingShingle Biodiversity
Taxonomy
Protozoa
Ciliophora
Kinetofragminophora
Trichostomatida
Blepharocorythidae
Diplodinium
Diplodinium cameli
Diplodinium cameli f. bispinatum
Kubesy, A. A.
Dehority, Burk A.
Diplodinium cameli subsp. f var. bispinatum Kubesy & Dehority, 2002, f. n.
topic_facet Biodiversity
Taxonomy
Protozoa
Ciliophora
Kinetofragminophora
Trichostomatida
Blepharocorythidae
Diplodinium
Diplodinium cameli
Diplodinium cameli f. bispinatum
description Diplodinium cameli f. bispinatum f. n. (Figs. 4­6) With all the characteristics of the species. Single spines arise from both the dorsal and ventral sides approximately five­sixths of the cell length towards the posterior end. The dorsal spine is well developed in most cells, averaging around 12 m, while the ventral spine ranges from about 5 to 12 m. The ventral spine tends to be slightly more pointed than the dorsal spine. This form only constituted 5.3 % of Diplodinium cameli cells in the three animals in which it occurred. Dimensions for this form are presented in Table 3. Although there were some differences in size for the different forms, they were not significant except for the higher L/W ratio of D. cameli f. bispinatum ( P <0.05). The environmental or nutritional pressures which might lead to the development of spines in Diplodinium cameli are not known. Coleman, Laurie and Baily (1977) observed that in vitro cultures of Entodinium bursa required the presence of Entodinium caudatum, which they engulfed as a food supply. Addition of the non­spinated forms of Entodinium caudatum resulted in the development of spined cells. Their E. caudatum cultures had been previously grown for 17 years in vitro as the spineless form. Although development of spines probably requires additional energy compared to the non­spinated form, they found that ingestion of the spined form was very limited compared to the spineless form. They concluded that spination was actually a defense mechanism. Because of its body size and the relatively small size of the spines, it would seem unlikely that Diplodinium cameli has developed the spines as a defense against predation. However, in ruminants the specific predation of large entodiniomorphs such as Eudiplodinium maggii by Polyplastron multivesiculatum has been well documented (Eadie 1962, 1967). Other than this, most observations suggest that predation among the protozoa is accidental and very limited (Lubinsky 1957). The absence of Polyplastron in the camels would seem to rule out the development of spination as a means to inhibit predation. Van Hoven (1975), studying rumen protozoa in the tsessebe (antelope) from South Africa, reported the presence of spines in the species Diplodinium costatum. Later, Dehority (1985) observed spined forms of D. costatum in rumen contents from musk­oxen in the Canadian arctic. Although Poljansky and Strelkow (1938) demonstrated that clone cultures in vivo of Entodinium caudatum were environmentally plastic and could be affected by diet it seems unlikely that this would explain the occurrence of spined forms in D. costatum. Diets would be quite different in these widely separated geographic locations. More recently, spined forms of Diplodinium rangiferi were observed in Australian red deer and in Japanese cattle which were inoculated with spineless forms of this species from sika deer (Dehority 1997; Imai et al. 2002). The spines observed in D. costatum and D. rangiferi cells are quite similar to those found in the different forms of D. anisacanthum (Dogiel 1927). That is, they arise at the caudal end of the cell. In contrast, the spines in D. cameli arise approximately one­sixth of the distance toward the anterior end of the cell, from the dorsal and ventral surfaces. The present study also revealed a wide variation in size, shape, and ciliary zones of Hsiungia triciliata and Polymorphella bovis , as well as several different forms of Entodinium ovumrajae. Further studies are required for possible redescription or establishment of new forms for these species. : Published as part of Kubesy, A. A. & Dehority, Burk A., 2002, Forestomach ciliate Protozoa in Egyptian dromedary camels (Camelus dromedarius), pp. 1-12 in Zootaxa 51 on pages 9-10, DOI: 10.5281/zenodo.155871 : {"references": ["Coleman, G. S., Laurie, J. I., & Baily, J. E. (1977) The cultivation of the rumen ciliate Entodinium bursa in the presence of Entodinium caudatum. Journal of General Microbiology, 101, 253 - 258.", "Eadie, J. M. (1962) Interrelationships between certain rumen ciliate protozoa. Journal of General Microbiology, 29, 579 - 588.", "Eadie, J. M. (1967) Studies on the ecology of certain rumen ciliate protozoa. Journal of General Microbiology, 49, 175 - 194.", "Lubinsky, G. (1957) Note on the phylogenetic significance of predatory habits in the Ophryoscolecidae (Ciliata: Oligotricha). Canadian Journal of Zoology, 35, 579 - 580.", "Van Hoven, W. (1975) Rumen ciliates of the tsessebe (Damaliscus lunatus lunatus) in South Africa. Journal of Protozoology, 22, 457 - 462.", "Dehority, B. A. (1985) Rumen ciliates of musk-oxen (Ovibos moschatus Z.) From the Canadian arctic. Journal of Protozoology, 32, 246 - 250.", "Poljansky, G. & Strelkow, A. (1938) Etude Experimentale sur la Variabilite de quelques Ophyryoscolecides. Archives de Zoologie Experimentale et Generale, 80, 1 - 123.", "Dehority, B. A. (1997) Rumen ciliate protozoa in Australian red deer (Cervus elephas L.). Archiv fur Protistenkunde, 148, 157 - 165.", "Imai, S., Matsumoto, M., Watanabe, A. & Sato, H. (2002) Establishment of a spinated type of Diplodinium rangiferi by transfaunation of the rumen ciliates of Japanese sika deer (Cervus nippon centralis) to the rumen of two Japanese shorthorn calves. Journal of Eukaryotic Microbiology, 49, 38 - 41.", "Dogiel, V. A. (1927) Monographie der familie Ophryoscolecidae. Archiv fur Protistenkunde, 59, 1 - 288."]}
format Text
author Kubesy, A. A.
Dehority, Burk A.
author_facet Kubesy, A. A.
Dehority, Burk A.
author_sort Kubesy, A. A.
title Diplodinium cameli subsp. f var. bispinatum Kubesy & Dehority, 2002, f. n.
title_short Diplodinium cameli subsp. f var. bispinatum Kubesy & Dehority, 2002, f. n.
title_full Diplodinium cameli subsp. f var. bispinatum Kubesy & Dehority, 2002, f. n.
title_fullStr Diplodinium cameli subsp. f var. bispinatum Kubesy & Dehority, 2002, f. n.
title_full_unstemmed Diplodinium cameli subsp. f var. bispinatum Kubesy & Dehority, 2002, f. n.
title_sort diplodinium cameli subsp. f var. bispinatum kubesy & dehority, 2002, f. n.
publisher Zenodo
publishDate 2002
url https://dx.doi.org/10.5281/zenodo.5586600
https://zenodo.org/record/5586600
long_lat ENVELOPE(163.400,163.400,-77.533,-77.533)
ENVELOPE(-44.616,-44.616,-60.733,-60.733)
ENVELOPE(163.033,163.033,-78.317,-78.317)
ENVELOPE(-55.942,-55.942,-61.479,-61.479)
geographic Arctic
Coleman
Laurie
Dromedary
Eadie
geographic_facet Arctic
Coleman
Laurie
Dromedary
Eadie
genre Arctic
ovibos moschatus
genre_facet Arctic
ovibos moschatus
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spelling ftdatacite:10.5281/zenodo.5586600 2023-05-15T15:19:29+02:00 Diplodinium cameli subsp. f var. bispinatum Kubesy & Dehority, 2002, f. n. Kubesy, A. A. Dehority, Burk A. 2002 https://dx.doi.org/10.5281/zenodo.5586600 https://zenodo.org/record/5586600 unknown Zenodo http://publication.plazi.org/id/6559FFC86D50994F7E6C532D2079F338 http://zoobank.org/6249708B-2C33-43CC-8959-39403DB6AE90 https://zenodo.org/communities/biosyslit https://dx.doi.org/10.5281/zenodo.155871 http://publication.plazi.org/id/6559FFC86D50994F7E6C532D2079F338 https://dx.doi.org/10.5281/zenodo.155872 http://zoobank.org/6249708B-2C33-43CC-8959-39403DB6AE90 https://dx.doi.org/10.5281/zenodo.5586599 https://zenodo.org/communities/biosyslit Open Access info:eu-repo/semantics/openAccess Biodiversity Taxonomy Protozoa Ciliophora Kinetofragminophora Trichostomatida Blepharocorythidae Diplodinium Diplodinium cameli Diplodinium cameli f. bispinatum Text Taxonomic treatment article-journal ScholarlyArticle 2002 ftdatacite https://doi.org/10.5281/zenodo.5586600 https://doi.org/10.5281/zenodo.155871 https://doi.org/10.5281/zenodo.155872 https://doi.org/10.5281/zenodo.5586599 2021-11-05T12:55:41Z Diplodinium cameli f. bispinatum f. n. (Figs. 4­6) With all the characteristics of the species. Single spines arise from both the dorsal and ventral sides approximately five­sixths of the cell length towards the posterior end. The dorsal spine is well developed in most cells, averaging around 12 m, while the ventral spine ranges from about 5 to 12 m. The ventral spine tends to be slightly more pointed than the dorsal spine. This form only constituted 5.3 % of Diplodinium cameli cells in the three animals in which it occurred. Dimensions for this form are presented in Table 3. Although there were some differences in size for the different forms, they were not significant except for the higher L/W ratio of D. cameli f. bispinatum ( P <0.05). The environmental or nutritional pressures which might lead to the development of spines in Diplodinium cameli are not known. Coleman, Laurie and Baily (1977) observed that in vitro cultures of Entodinium bursa required the presence of Entodinium caudatum, which they engulfed as a food supply. Addition of the non­spinated forms of Entodinium caudatum resulted in the development of spined cells. Their E. caudatum cultures had been previously grown for 17 years in vitro as the spineless form. Although development of spines probably requires additional energy compared to the non­spinated form, they found that ingestion of the spined form was very limited compared to the spineless form. They concluded that spination was actually a defense mechanism. Because of its body size and the relatively small size of the spines, it would seem unlikely that Diplodinium cameli has developed the spines as a defense against predation. However, in ruminants the specific predation of large entodiniomorphs such as Eudiplodinium maggii by Polyplastron multivesiculatum has been well documented (Eadie 1962, 1967). Other than this, most observations suggest that predation among the protozoa is accidental and very limited (Lubinsky 1957). The absence of Polyplastron in the camels would seem to rule out the development of spination as a means to inhibit predation. Van Hoven (1975), studying rumen protozoa in the tsessebe (antelope) from South Africa, reported the presence of spines in the species Diplodinium costatum. Later, Dehority (1985) observed spined forms of D. costatum in rumen contents from musk­oxen in the Canadian arctic. Although Poljansky and Strelkow (1938) demonstrated that clone cultures in vivo of Entodinium caudatum were environmentally plastic and could be affected by diet it seems unlikely that this would explain the occurrence of spined forms in D. costatum. Diets would be quite different in these widely separated geographic locations. More recently, spined forms of Diplodinium rangiferi were observed in Australian red deer and in Japanese cattle which were inoculated with spineless forms of this species from sika deer (Dehority 1997; Imai et al. 2002). The spines observed in D. costatum and D. rangiferi cells are quite similar to those found in the different forms of D. anisacanthum (Dogiel 1927). That is, they arise at the caudal end of the cell. In contrast, the spines in D. cameli arise approximately one­sixth of the distance toward the anterior end of the cell, from the dorsal and ventral surfaces. The present study also revealed a wide variation in size, shape, and ciliary zones of Hsiungia triciliata and Polymorphella bovis , as well as several different forms of Entodinium ovumrajae. Further studies are required for possible redescription or establishment of new forms for these species. : Published as part of Kubesy, A. A. & Dehority, Burk A., 2002, Forestomach ciliate Protozoa in Egyptian dromedary camels (Camelus dromedarius), pp. 1-12 in Zootaxa 51 on pages 9-10, DOI: 10.5281/zenodo.155871 : {"references": ["Coleman, G. S., Laurie, J. I., & Baily, J. E. (1977) The cultivation of the rumen ciliate Entodinium bursa in the presence of Entodinium caudatum. Journal of General Microbiology, 101, 253 - 258.", "Eadie, J. M. (1962) Interrelationships between certain rumen ciliate protozoa. Journal of General Microbiology, 29, 579 - 588.", "Eadie, J. M. (1967) Studies on the ecology of certain rumen ciliate protozoa. Journal of General Microbiology, 49, 175 - 194.", "Lubinsky, G. (1957) Note on the phylogenetic significance of predatory habits in the Ophryoscolecidae (Ciliata: Oligotricha). Canadian Journal of Zoology, 35, 579 - 580.", "Van Hoven, W. (1975) Rumen ciliates of the tsessebe (Damaliscus lunatus lunatus) in South Africa. Journal of Protozoology, 22, 457 - 462.", "Dehority, B. A. (1985) Rumen ciliates of musk-oxen (Ovibos moschatus Z.) From the Canadian arctic. Journal of Protozoology, 32, 246 - 250.", "Poljansky, G. & Strelkow, A. (1938) Etude Experimentale sur la Variabilite de quelques Ophyryoscolecides. Archives de Zoologie Experimentale et Generale, 80, 1 - 123.", "Dehority, B. A. (1997) Rumen ciliate protozoa in Australian red deer (Cervus elephas L.). Archiv fur Protistenkunde, 148, 157 - 165.", "Imai, S., Matsumoto, M., Watanabe, A. & Sato, H. (2002) Establishment of a spinated type of Diplodinium rangiferi by transfaunation of the rumen ciliates of Japanese sika deer (Cervus nippon centralis) to the rumen of two Japanese shorthorn calves. Journal of Eukaryotic Microbiology, 49, 38 - 41.", "Dogiel, V. A. (1927) Monographie der familie Ophryoscolecidae. Archiv fur Protistenkunde, 59, 1 - 288."]} Text Arctic ovibos moschatus DataCite Metadata Store (German National Library of Science and Technology) Arctic Coleman ENVELOPE(163.400,163.400,-77.533,-77.533) Laurie ENVELOPE(-44.616,-44.616,-60.733,-60.733) Dromedary ENVELOPE(163.033,163.033,-78.317,-78.317) Eadie ENVELOPE(-55.942,-55.942,-61.479,-61.479)