Chilotrogus matejiceki Miessen, Uliana & Keith, 2020
publication ID |
https://doi.org/ 10.11646/zootaxa.4742.1.12 |
publication LSID |
lsid:zoobank.org:pub:B4C86DC6-6213-4405-9F5B-47A2E0EC9C32 |
DOI |
https://doi.org/10.5281/zenodo.3681155 |
persistent identifier |
https://treatment.plazi.org/id/46973C58-9546-4BD6-872E-228027A68496 |
taxon LSID |
lsid:zoobank.org:act:46973C58-9546-4BD6-872E-228027A68496 |
treatment provided by |
Plazi |
scientific name |
Chilotrogus matejiceki Miessen, Uliana & Keith |
status |
sp. nov. |
Chilotrogus matejiceki Miessen, Uliana & Keith , new species
( Figs. 2 View FIGURES 1–4 , 5 View FIGURES 5–8 , 14–18 View FIGURES 14–18 , 21, 22 View FIGURES 19–22 , 25, 26 View FIGURES 23–26 , 29, 30 View FIGURES 27–30 , 45 View FIGURES 45, 46 , 47 View FIGURE 47 )
Type material (9♂♂ and 3♀♀). Holotype, ♂ ( NMPC) labelled: “ E. Iran, Deh Bakhri | 1700—1750 m | 30.4– 3.5.1973 [printed] || Loc. no. 186 | Exp. Nat. Mus. | Praha [printed] || Chilotrogus [handwritten] | panotrogoides [handwritten] | Rtt. [handwritten] D Keith det [20]07 [printed]” . Paratypes: 1♂ ( CRS, CGM), same data as holotype ; 4♂♂ and 1♀ ( CMU, CJM): “dat. 27- 28.5.2014 Irán IR | Kerman prov. | Mijam ( Jiroft ) | N 28°52’29” E 57°53’01” | leg. Černý Fr., 1650 m.n.m. [printed]” GoogleMaps ; 2♂♂ and 1♀ ( CRS, CGM): “ IRAN, Kerman prov. | 5 km S. Deh Bakhri | 28°59’N 57°55’E, 2300 m | 31. V.1997, A. Hofmann lgt.” GoogleMaps ; 1♂ and 1♀ (allotypus) ( CRS), same data, but “ 31. V–1. VI.1997, leg. A. Hofmann & P. Kautt ” GoogleMaps .
Description of the holotype (♂). Length 16.6 mm. Habitus dark brown and matt ( Fig. 5 View FIGURES 5–8 ). Clypeus and forehead with large, strong and dense punctuation and traces of microscopic pilosity on the edges. Clypeus slightly larger than the distance between the eyes. Antennae with ten antennomeres, trimerous antennal club short, as long as funicle and scape together.
Pronotum glabrous with large, strong, dense and deep punctuation, the punctures slightly more spaced than those on clypeus and forehead. Lateral margins crenulate with thick setae, slightly shorter than those of epipleuron in the humeral area.
Elytra matt, pruinose with coarse punctuation, sparser on the interstriae. Pilosity very short and sparse, distributed over the entire surface. Epipleuron with long and thick pilosity, gradually shortening towards apex.
Protibiae tridentate, the basal tooth at the middle, the median tooth slightly closer to the apical. Inner spur inserted slightly behind the median tooth. Metatarsi elongate, 1.8 times longer than metatibiae which are dented on upper face. At the base of each dent is one thick and long seta.
Pygidium with raised setae in lateral view.
Aedeagus of characteristic shape; parameres ( Figs. 14–16 View FIGURES 14–18 ) in dorsal view with a marked angle at the level of the central opening. Internal piece broadly open dorsally, exposing an internal tubular structure that bears a backwards protruding spine at the apex ( Figs. 17, 18 View FIGURES 14–18 , 25 View FIGURES 23–26 ).
Variability of males. Length: 16.1–17.5 mm. Parameres in dorsal view with the marked angle at the level of the central opening more or less developed ( Figs. 21, 22 View FIGURES 19–22 ), internal piece also variable ( Figs. 25, 26 View FIGURES 23–26 ).
Female. Length: 15.7–16.1 mm. Similar to male, but antennal club shorter, as well as the metatarsi.
Etymology. Dedicated to Jan Matějíček (Hradec Králové, Czech Republic), a specialist on Staphylinidae and keen collector of Scarabaeoidea, who entrusted one of us (MU) with the first specimen that we study.
Distribution. Currently only known from three nearby collecting sites on Jebal Barez mountain range, in southeastern Iran, between 1650 and 2300 m a.s.l. ( Fig. 47 View FIGURE 47 ).
Differential diagnosis. Chilotrogus matejiceki new species appears to be externally indistinguishable from Ch. panotrogoides (cf. habitus in Figs. 2 View FIGURES 1–4 , 5 View FIGURES 5–8 and 1 View FIGURES 1–4 , 6 View FIGURES 5–8 ), and identification can be achieved only by examination of the male genitalia (cf. Figs. 9–13 View FIGURES 9–13 and 14–18 View FIGURES 14–18 ). Parameres of Ch. matejiceki new species are characterised by an angled to tooth-like projection of the internal margin, which marks the distal part of a broad basal concavity. The type series shows some degree of variability (including between syntopic specimens) in this trait (cf. Figs. 21, 22 View FIGURES 19–22 ), that is however well distinct from the gently curved morphology of Ch. panotrogoides ( Figs. 19, 20 View FIGURES 19–22 ). Additional differences are found in the distal part of the internal sclerite. Its dorsal spine is variable in elongation in both species, but in Ch. matejiceki new species it is broad at the base and flattened in its distal part ( Figs. 25, 26 View FIGURES 23–26 ), while in Ch. panotrogoides the same spine is narrow at the base and is cylindrical in its distal part ( Figs. 23, 24 View FIGURES 23–26 ). Also, the subcircular apex of the tube-like structure that bears the spine is almost completely occupied by soft tissue (evertible part of endophallus) in Ch. panotrogoides ( Figs. 23c, 24c View FIGURES 23–26 ), while the same soft tissue occupies only about the lower half of the apex in Ch. matejiceki new species ( Figs. 25c, 26c View FIGURES 23–26 ).
Females of the two species show very moderate differences in the genital sclerites ( Figs. 27–30 View FIGURES 27–30 ), whose diagnostic value should be verified on a longer series.
NMPC |
National Museum Prague |
CMU |
Chiang Mai University |
V |
Royal British Columbia Museum - Herbarium |
VI |
Mykotektet, National Veterinary Institute |
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 |
Melolonthinae |
Tribe |
Rhizotrogini |
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