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Type species of the podoo phryid, phalacrocleptid and metacinee tid suctorian genera. A-Parapoo dophrya soliformis (Lauterborn, 1901), from Kahl, 1931; B-Podophrya fixa (Muller, 1786), orig.; C-Sphaeroo phrya magna Maupas, 1881, orig.; DVanhovenia multisuctores (Van Hoven et al., 1998), from Van Hoven et al., 1998; E-Allantosoma intestinalis Gassowski, 1918, orig.; F-Arcosoma dicorniger (Hsiung, 1928), from Kudo, 1946; G-Allantoxena biseriale (Strelkow, 1939), from Ike et al., 1983; HSeveronis spongiarum Jankowski, 1981, from Jankowski, 1981; I-Phalacroo cleptes verruciformis Kozloff, 1966, from Jankowski, 1981; J-Metacineta mystacina (Ehrenberg, 1831), orig.; K-Urnula epistylidis Claparede et Lachh mann, 1861, orig.; L-Paracineta paa tula (Claparede et Lachmann, 1861), budding, from Collin, 1912; MActinocyathula cidaris (Kent, 1882), from Kahl, 1934.

Type species of the podoo phryid, phalacrocleptid and metacinee tid suctorian genera. A-Parapoo dophrya soliformis (Lauterborn, 1901), from Kahl, 1931; B-Podophrya fixa (Muller, 1786), orig.; C-Sphaeroo phrya magna Maupas, 1881, orig.; DVanhovenia multisuctores (Van Hoven et al., 1998), from Van Hoven et al., 1998; E-Allantosoma intestinalis Gassowski, 1918, orig.; F-Arcosoma dicorniger (Hsiung, 1928), from Kudo, 1946; G-Allantoxena biseriale (Strelkow, 1939), from Ike et al., 1983; HSeveronis spongiarum Jankowski, 1981, from Jankowski, 1981; I-Phalacroo cleptes verruciformis Kozloff, 1966, from Jankowski, 1981; J-Metacineta mystacina (Ehrenberg, 1831), orig.; K-Urnula epistylidis Claparede et Lachh mann, 1861, orig.; L-Paracineta paa tula (Claparede et Lachmann, 1861), budding, from Collin, 1912; MActinocyathula cidaris (Kent, 1882), from Kahl, 1934.

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Citations

... A number of suctorian and peritrich ciliates are epibionts on marine and freshwater invertebrates such as copepods, cladocerans, nematodes, halacarid and hydrachnidid mites (eg. Precht 1935;Jankowski 1981Jankowski , 2007Dovgal 1996Dovgal , 2002Dovgal et al. 2008aDovgal et al. , b, 2009aFernandezLeborans & Tato-Porto 2000a, b;Ingole et al. 2010;Fernandez-Leborans et al. 2012;Chatterjee et al. 2012Chatterjee et al. , 2013aChatterjee et al. , b, 2014). The ciliate infestation on small fauna may affect their competitive ability, reproduction, locomotion, and bioenergetics (Chatterjee 1996). ...
... Several studies stressed that the intensity and rate of infestation varies between different species and between populations of the same species ( Dovgal et al. 2002;Bartsch & Dovgal 2010). All specimens of Halacarellus discretus, collected in shallow water sandy deposits near Odessa (Black Sea) were infested Thecacineta calix with 8-62 ciliates per host specimen (Bartsch & Dovgal 2010). ...
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Based on published records and original data, a list of the epibiont suctorian and peritrich ciliates (Ciliophora) on halacarid and hydrachnid mites is presented. Altogether 13 suctorian and 10 peritrich species from hydrachnid and halacarid mites were listed. From this list, six suctorian and one peritrich species have been reported from halacarid mites, while four suctorian and four peritrich species were found on hydrachnid mites determined up to species level. The remaining specimens were determined upto the generic level. The halacarid and hydrachnid species do not share any suctorian and peritrich species and some of the ciliate species are specific to certain taxonomic groups of the hosts.The host specificity of both suctorian and peritrich ciliates, localization on the host body and environment are discussed. Some ciliate species specific to hydrachnid mites prefer lotic or lentic habitats. In most cases, both suctorian and peritrich ciliates prefer only marine or only fresh water bodies. It was also mentioned that both suctorian and peritrich ciliates have not distinct preferences in localization on their host body.
... A number of suctorian and peritrich ciliates are epibionts on marine and freshwater invertebrates such as copepods, cladocerans, nematodes, halacarid and hydrachnidid mites (eg. Precht 1935;Jankowski 1981Jankowski , 2007Dovgal 1996Dovgal , 2002Dovgal et al. 2008aDovgal et al. , b, 2009aFernandezLeborans & Tato-Porto 2000a, b;Ingole et al. 2010;Fernandez-Leborans et al. 2012;Chatterjee et al. 2012Chatterjee et al. , 2013aChatterjee et al. , b, 2014). The ciliate infestation on small fauna may affect their competitive ability, reproduction, locomotion, and bioenergetics (Chatterjee 1996). ...
... Several studies stressed that the intensity and rate of infestation varies between different species and between populations of the same species ( Dovgal et al. 2002;Bartsch & Dovgal 2010). All specimens of Halacarellus discretus, collected in shallow water sandy deposits near Odessa (Black Sea) were infested Thecacineta calix with 8-62 ciliates per host specimen (Bartsch & Dovgal 2010). ...
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... В связи с этим, настоящее сообщение содержит предварительную оценку специфичности к хозяевам отмеченных в подземных водах комменсальных и паразитических цилиат из классов Suctorea Claparede et Lachmann, 1859 За основу в данной статье принята система типа Ciliophora Д. Линна (Lynn, 2008) за исключением класса Suctorea, для которого применялась система И.В. Довгаля (Довгаль, 2013;Dovgal, 2002). ...
... У их расселительных стадий (бродяжек, томитов) имеется только локомоторная цилиатура, либо инфрацилиатура (базальные тельца ресничек). Характерный для большинства цилиат ротовой аппарат отсутствует функция питания выполняется щупальцами с осевым скелетом (аксонемой) из микротрубочек (Довгаль, 2013;Dovgal, 2002). ...
... Дж. Матьяшич (Matjašič, 1956) впервые установил, что S. troglocaridis размножается путем формирования своеобразных червеобразных безресничных бродяжек. Однако, данный тип почкования (вермигеммия) характерен для сукторий из разных местообитаний, не только пещерных (Довгаль, 2013;Dovgal, 2002). Впоследствии S. troglocaridis была найден в пещере Нижняя Шакуранская, Западный Кавказ, Абхазия (Dovgal, Vargovitsh, 2010) на креветках Troglocaris sp. ...
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... The redescriptions of these ciliates with attention to poorly studied stylotheca structure in suctorian ciliate and macronucleus morphology in peritrich are presented. The systematic position of suctorian ciliate have been given afterDovgal (2002Dovgal ( , 2013) whereas systematics of peritrich ciliate have been shown after Lynn (2008). ...
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... Classification and identification of species was based on previously published species descriptions and taxonomic lists (Dovgal 2002;Gürelli and Ito 2014;Ito et al. 2010Ito et al. , 2011Latteur 1967;Latteur et al. 1970;Lynn 2008;Imai 1995, 1997;Wolska 1967Wolska , 1968Wolska 1971Wolska , 1986. ...
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... ) in representatives of Loricophrya is shorter than the lorica itself (in contrast with the relative genus Paracineta Collin, 1911). Dovgal (2002) has added the information on the mode of reproduction in some Loricophrya's species and proposed the latter generic diagnosis: ...
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... The term epibiont comprises organisms that, during the sessile phase of their life cycle, are fixed to the surface of a living substratum, while the basibiont carries and constitutes a support for the epibiont (Threlkeld et al. 1993). An important number of ciliates have been described as epibionts in many crustacean groups such as amphipods, branchiopods, copepods, ostracods, mysids, euphausiids or decapods (Fernandez-Leborans et al. 1997, 2002Fernandez-Leborans andTato-Porto 2000a,b, 2002). Some of these crustaceans may constitute an important part of the zooplankton , which act as substrata for the epibionts and also as intermediate or final hosts of different parasite species (Chatton 1920;Ho and Perkins 1985;Fernandez-Leborans and Tato-Porto 2002;Skovgaard et al. 2005Skovgaard et al. , 2007Skovgaard et al. , 2012Skovgaard and Saiz 2006;G omez et al. 2009;Gregori et al. 2012Gregori et al. , 2013. ...
... The 18S rRNA has been broadly used as a taxonomic tool to clarify the taxonomy of phyllopharyngean ciliates at different taxonomic levels, from species (Li and Song 2006;Gong et al. 2008Gong et al. , 2009Pan et al. 2012) to higher rank relationships (Rylei and Katz 2001;Snoeyenbos-West et al. 2004;Zhao et al. 2013). Despite the extraordinary diversity of forms displayed by these ciliates, both morphologic (Dovgal 1996(Dovgal , 2002Lynn 2008) and genetic works (Snoeyenbos-West et al. 2004;Zhao et al. 2013) confirmed that the phyllopharyngean subclass is a monophyletic clade containing three major orders, according to their mode of asexual reproduction: Evaginogenina, Exogenina and Endogenina. ...
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