Eulaelaps kolpakovae Bregetova, 1950
publication ID |
https://doi.org/ 10.11646/zootaxa.4273.1.1 |
publication LSID |
lsid:zoobank.org:pub:FED562EC-7139-485D-BB6F-6D18769F47C3 |
DOI |
https://doi.org/10.5281/zenodo.6023608 |
persistent identifier |
https://treatment.plazi.org/id/03C31742-FFB1-423C-FF40-FF13FCE7FB8F |
treatment provided by |
Plazi |
scientific name |
Eulaelaps kolpakovae Bregetova, 1950 |
status |
|
Eulaelaps kolpakovae Bregetova, 1950
Eulaelaps kolpakovae Bregetova, 1950: 13 , fig. 1.
Eulaelaps kolpakovae .— Bregetova, 1955: 319, figs 649, 651, 655–659; Bregetova, 1956a: 102, figs 172, 176, 179-182; Lange, 1958: 201, pl. LXXI, G; Strandtmann & Wharton, 1958: 128; Piryanik, 1962: 84; Allred, 1969: 108, fig. P-4; Senotrusova, 1987: 150, fig. 73; Goncharova et al., 1991: 24.
Eulaelaps novus.— Evans & Till, 1966: 263, fig. 62 (partim); Evans & Till, 1979: 239, fig. 33, g, h, k (partim); Karg, 1993: 166 (partim); Mašán & Fend’a, 2010: 108, figs 105, 106, 109 (partim).
Type locality. Russia, Astrakhan’ Region, Staryi Tuzukley settlement.
Type specimens. ZIN. The type specimens included 12 syntypes (females only), now only ten of them (eight slides) remain in the collection.
Type host. Arvicola terrestris (L., 1758), the European water vole.
Host range. This species is a predatory mite with a weak tendency towards hematophagy ( Goncharova et al., 1991). It has been collected from a wide spectrum of rodents and insectivores (mainly from their burrows) and birds (from nests). Eu. kolpakovae does not demonstrate a specific relationship with any particular species of mammal hosts ( Goncharova et al., 1991).
Distribution. Southern part of Eastern Europe, the Urals, Central Asia, southern Siberia and the Russian Far East. Its distribution in Asiatic Russia roughly coincides with that of Eu. cricetuli ( Nikulina, 2004) .
Remarks. Evans & Till (1966) proposed to synonymise Eulaelaps kolpakovae with Eu. novus Vitzthum, 1925. This opinion was accepted by Karg (1971), Haitlinger (1988) and Mašán & Fend’a (2010), among others. However, Senotrusova (1976, 1987) and Goncharova et al. (1991) provided additional morphological evidence in favour Eu. kolpakovae as a separate species. Mašán & Fend’a (2010), in their discussion of the taxonomic position of Eu. kolpakovae , did not consider these arguments. Senotrusova (1976, 1987) believes that Eu. novus is merely an intraspecific form of Eu. stabularis . According to Strandtmann & Wharton (1958), Vitzthum, the author of the species Eu. novus, also assumed that this taxon may represent ‘a small form of stabularis ’. Thus, the taxonomic status of these two species needs a new revision. Sludsky (2014) listed Eu. kolpakovae among mite species able to harbour Yersinia pestis – the causative agent of the plague.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
Kingdom |
|
Phylum |
|
Class |
|
Order |
|
InfraOrder |
Gamasina |
Family |
|
Genus |
Eulaelaps kolpakovae Bregetova, 1950
Vinarski, Maxim V. & Korallo-Vinarskaya, Natalia P. 2017 |
Eulaelaps
Karg 1993: 166 |
Evans 1979: 239 |
Evans 1966: 263 |
Eulaelaps kolpakovae
Goncharova 1991: 24 |
Senotrusova 1987: 150 |
Allred 1969: 108 |
Piryanik 1962: 84 |
Lange 1958: 201 |
Strandtmann 1958: 128 |
Bregetova 1956: 102 |
Bregetova 1955: 319 |
Eulaelaps kolpakovae
Bregetova 1950: 13 |