Quedius kalabi Smetana, 1995
publication ID |
https://doi.org/ 10.5852/ejt.2018.401 |
publication LSID |
lsid:zoobank.org:pub:9C9DB157-AAA5-40B7-BA0B-9A57779382C1 |
DOI |
https://doi.org/10.5281/zenodo.5695866 |
persistent identifier |
https://treatment.plazi.org/id/03D5FE7E-7043-BF27-FD93-F98CFBC9FA50 |
treatment provided by |
Plazi |
scientific name |
Quedius kalabi Smetana, 1995 |
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Quedius kalabi Smetana, 1995 View in CoL
Figs 1 View Fig.1 , 3 View Fig.3 , 4C–D View Fig. 4
Quedius kalabi Smetana, 1995: 77 View in CoL (original description).
Quedius kalabi View in CoL – Smetana 1998: 118 (comparison with Q. mutilatus View in CoL ). — Solodovnikov & Hansen 2016: 7 (distribution).
Material examined
Type material
KYRGYZSTAN: Holotype, ♂, “ SU – Tien Shan NE part of Terskey Ala Too [Terskei Alatau] ridge 3000–3600 m ” ( NMW).
Additional material
KYRGYZSTAN: 1 ♂, 1 ♀, E TerskeiAlatau , Teploklyuchenka Village, 2600 m [42.4400° N, 78.5200° E], 16 Jun. 1993, S. Ovchinnikov leg. ( cSch). GoogleMaps
Distribution and bionomics
Quedius kalabi is known from the three specimens examined here, collected in the Terskei Alatau mountain range at high elevations around 2600–3600 m ( Fig. 1 View Fig.1 ). Only two of them bear labels that specify the date and exact collecting locality (16 Jun. 1993, Teploklyuchenka Village). All previously published material for Q. kalabi , except the holotype, but including the paratype, was apparently misidentified (see below). Like other species of the Q. mutilatus group, Q. kalabi presumably occurs in talus-associated microhabitats.
Notes on the type material
Smetana (1995) based his description of Q. kalabi on the holotype (male, see above for details) and one paratype (female, for information see the undetermined or ambiguous material at the end of this paper), both from the north-eastern part of Terskei Alatau. The precise geographic origin of the holotype is unknown, while the paratype comes from a locality called Jety Oguz. The aedeagus preparation of the holotype of Q. kalabi in Canada balsam allows an examination of its lateral side, not illustrated in Smetana (1995) ( Fig. 3B View Fig.3 ). It confirms our identification of Q. kalabi , which differs from other species of the Q. mutilatus group by its narrower and somewhat curved apical portion of the median lobe of the aedeagus, with a relatively short blade of its subapical tooth (aedeagus in lateral view). In the shape of the apical portion of the paramere and degree of its incision, Q. kalabi displays a transition between Q. mutilatus with a less incised paramere bearing more lateral peg setae, and Q. equus with a more incised paramere bearing fewer lateral peg setae. The characters indicated by Smetana (1988) in a comparison of Q. kalabi with Q. mutilatus were based, as revealed here, on non-conspecific males and females of both species. They do not align with the more extensive material examined here. The collecting locality of the paratype of Q. kalabi is, in fact, located closer to the distribution area of Q. mutilatus . Except for the holotype, the distributional records of Q. kalabi summarized in Solodovnikov & Hansen (2016) were based on misidentified specimens of Q. mutilatus . The specimens of Q. kalabi from Teploklyuchenka Village, examined here and compared with the holotype, are the first precisely georeferenced material for this species. Based on the shape of aedeagus, three possibly mislabeled specimens from Toksanbai in Dzungarian Alatau seem to belong to Q. kalabi as well (for details see below).
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.
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SubFamily |
Staphylininae |
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Staphylinini |
SubTribe |
Quediina |
Genus |
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SubGenus |
Microsaurus |
Quedius kalabi Smetana, 1995
Salnitska, Maria & Solodovnikov, Alexey 2018 |
Quedius kalabi
Solodovnikov 2016: 7 |
Smetana 1998: 118 |
Quedius kalabi
Smetana 1995: 77 |