Dima pelionensis, Mertlik, Josef, Németh, Tamás & Kundrata, Robin, 2017
publication ID |
https://doi.org/ 10.11646/zootaxa.4220.1.1 |
publication LSID |
lsid:zoobank.org:pub:D74BC90C-84CC-4788-9048-54F5C8521B32 |
DOI |
https://doi.org/10.5281/zenodo.4670904 |
persistent identifier |
https://treatment.plazi.org/id/039687B0-FFBA-FFEE-C8C6-FE7B3929ACCD |
treatment provided by |
GgServerImporter |
scientific name |
Dima pelionensis |
status |
sp. nov. |
Dima pelionensis sp. nov.
Figs 92–95 View FIGURES 90 – 104 , 152–153 View FIGURES 143 – 154 , 209 View FIGURES 202 – 211 , 238 View FIGURES 234 – 242 , 245 View FIGURE 245 .
Type material. Holotype: GREECE: distr. Magnissia, Mt. Pilio, Chania env., 39°23'52.96'', 23°3'24.54''E, 1263 m, singled at night from ground, 11.VI.2015, ♂, leg. P. Brůha, J. Mertlik, T. Németh & B. Zbuzek ( HNHM) . Paratypes: GREECE: same data as holotype, 8 ♂♂, 6 ♀♀ ( HNHM) ; dtto, 20 ♂♂, 9 ♀♀ (PCRK); dtto, 19 ♂♂, 18 ♀♀, J. Mertlik leg. (PCJM); dtto, 6 ♂♂, 5 ♀♀, B. Zbuzek leg. (PCBZ); dtto, 2 ♂♂, 3 ♀♀, P. Brůha leg. (PCPB); Agios Onoufrios (Volos), 10.VI.2013, 1 ♂, 1 ♀, M. Malavasi leg. ( PCGP) ; Mt. Pelio, Chania env., 1133 m (N39°23'37", E23°02'39"), 3.VI.2011, 1 ♂, J. Krátký leg. ( PCJM) GoogleMaps ; distr. Magnissia, Mt. Pilio, Chania village env., 1263 m (39°23'52.96"N, 23°03'24.54"E), 15.VI.2012, 1 ♂, 1 ♀, M. Samek leg. ( PCMS) GoogleMaps ; dtto, 35 ♂♂, 30 ♀♀, J. Mertlik leg. (PCJM); dtto, 1 ♀ (PCRK); dtto, 10 ♂♂, 24 ♀♀, V. Dušánek leg. (PCVD); dtto, 17 ♂♂, 17 ♀♀, P. Brůha leg. (PCPB); dtto, 15 ♂♂, 17 ♀♀, B. Zbuzek leg. (PCBZ); Thessalia, Volos, Mt. Pilion , 1100 m, 7.VI.1985, 1 ♂, 1 ♀, G. Etonti leg. (as D. hladilorum in Schimmel & Platia 2008 ) ( PCGP) ; Magnissia, O. Pilio, 900 m, str. Hánia-Makriráhi , 13.VI.1991 / 7.VI.1992, 2 ♀♀, leg. P. M. Giachino & D. Vailati (paratypes of D. fokidensis ) ( PCGP, PCRS) .
Diagnosis. Dima pelionensis is a medium-sized species (body length: 10.5–14.0 mm), with sparsely punctate shiny pronotum with sides bearing decumbent pubescence in the anterior two thirds and semi-erect setae in the posterior third ( Figs 152–153 View FIGURES 143 – 154 ). Dima fthiotidensis and D. evritaniensis differ from D. pelionensis by the denser elytral pubescence ( Figs 26–28 View FIGURES 15 – 29 , 35–41 View FIGURES 30 – 44 ), pronotum matt, with denser and finer punctation ( Figs 126–127, 130– 134 View FIGURES 119 – 130 View FIGURES 131 – 142 ), and more or less convex scutellum (in lateral view) with more steeply declined frontal margin. Additionally, D. evritaniensis , D. etoliensis and D. zbuzeki sp. nov. have the semi-erect pubescence along the whole length of the pronotal sides ( Figs 125–127 View FIGURES 119 – 130 , 162 View FIGURES 155 – 162 ). Dima hladilorum has a more convex scutellum and more robust apical lobe of paramera ( Fig. 190 View FIGURES 182 – 191 ) and D. zbuzeki sp. nov. is smaller and has distinctly longer apical lobe of paramera ( Fig. 221 View FIGURES 212 – 221 ).
Description. Holotype, male. Body medium-sized, 12.8 mm long, 5.1 mm wide, matt, covered with very short dense pubescence. Body dark brown, with paler, reddish-brown antennae, legs, elytral outer margins and suture; pubescence yellowish ( Fig. 92 View FIGURES 90 – 104 ).
Head including eyes 0.6 times as wide as pronotum, frons with shallow depression; punctation dense and coarse, intervals between punctures dull; pubescence on head semi-erect, more erect in anterior part of frons, directed forwards. Supraantennal carina weakly defined. Antennae moderately long, surpassing the posterior angles of pronotum by more than three segments; antennomeres II–III subtriangular, about 1.5 times longer than wide, II slightly longer than III, together 1.2 times longer than antennomere IV, length ratio of antennomeres II–IV 1.1: 1.0: 1.9, antennomeres IV–X gradually widened apically, slightly more than 2 times longer than wide, apical antennomere subacute apically; surface of antennomeres covered with moderately long, semi-erect setae.
Pronotum 1.4 times wider than long, widest at middle, moderately convex dorsally; sides evenly convex, gradually slightly curved anteriorly in lateral view; anterior angles obtuse; posterior angles prominent, sharp, distinctly produced outward; punctation dense, fine, shallow, punctures on disc equally distributed, of about the same size; intervals between punctures shorter or of the same length as a diameter of puncture, shiny, more flattened posteriorly. Pubescence on pronotal disc very short, decumbent; that on sides decumbent at the anterior two thirds and semi-erect at the posterior third, longer setae at hind angles ( Fig. 152 View FIGURES 143 – 154 ). Prosternum finely punctate, with short decumbent to semi-erect setae; prosternal lobe moderately coarsely punctate, with longer pubescence.
Scutellum heart-shaped, flattened, in lateral view slightly raised above the plane of elytra, widest at two thirds; frontal margin rounded in lateral view, gradually declined; apex widely rounded, punctation fine, dense; pubescence fine, moderately long, semi-erect. Elytra sub-parallel, 3.3 times longer than pronotum, moderately convex, widest at middle, from middle gradually narrowing towards apex; striae well developed along the whole elytral length; surface of interstices flattened, moderately shiny, densely and finely punctate; punctures suboval, equally distributed, of the same size; pubescence short, dense.
Aedeagus elongate; paramera long, narrow, its apical lobe robust, subapical tooth short, blunt ( Fig. 209 View FIGURES 202 – 211 ).
Female ( Figs 93–95 View FIGURES 90 – 104 ). Like male, but with suboval body, shorter antennae (surpassing the posterior angles of pronotum about two segments), head 0.5 times as wide as pronotum, pronotum wider than in male (1.5 times wider than long), scutellum wider. The sclerotized spines of bursa copulatrix as in Fig. 238 View FIGURES 234 – 242 .
Intraspecific variability. Some specimens have rugose, more convex and more densely punctate pronotum ( Fig. 94 View FIGURES 90 – 104 ), similarly as in some other Dima species (e.g. D. fthiotidensis , D. scutellaris ). Body coloration is variable; some specimens have paler, reddish-brown some parts of body, e.g. antennae, pronotum, legs.
Distribution. Greece (Thesally: Mt. Pelion; Fig. 245 View FIGURE 245 ).
Etymology. The name " pelionensis " refers to Mt. Pelion, Greece, the type locality of the new species.
Remark. Schimmel & Platia (2008) described D. fokidensis with the holotype from Mt. Iti and paratypes from Mt. Pelion. That holotype is conspecific with D. fthiotidensis and the paratypes are here assigned to D. pelionensis sp. nov. ( Fig. 95 View FIGURES 90 – 104 ).
HNHM |
Hungarian Natural History Museum (Termeszettudomanyi Muzeum) |
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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