Orius (Xylorius) paveli, Yasunaga & Yamada & Duwal, 2019
publication ID |
https://doi.org/ 10.2478/aemnp-2019-0030 |
publication LSID |
lsid:zoobank.org:pub:5E55F4ED-2892-4265-B8CB-89D65BAFCA70 |
DOI |
https://doi.org/10.5281/zenodo.4505075 |
persistent identifier |
https://treatment.plazi.org/id/3B55375F-940F-FFEA-FEF7-FC453E33302D |
treatment provided by |
Felipe |
scientific name |
Orius (Xylorius) paveli |
status |
sp. nov. |
Orius (Xylorius) paveli sp. nov.
( Figs 5–6 View Figs 1–6 , 10 View Figs 7–12 , 15–16, 19–20 View Figs 13–21 , 46–60 View Figs 46–60 , 64–65 View Figs 61–65 )
Type material. HOLOTYPE: ♁, NEPAL: RASUWA DIST.: Langtang Himal National Park, Lama Hotel , 2,500 m alt., 28°09′43″N 85°25′49″E, leaves and stems of Urtica (prob.) dioica L., 8 June 2016, T.Yasunaga ( NMTU) (AMNH_PBI 00380640). GoogleMaps PARATYPES: NEPAL: RASUWA DIST.: Langtang Himal National Park, same data as for holotype, 2 ♁♁ 16 ♀♀ ( AMNH, TKPM, TYCN); Syabru Besi~Bamboo, 28°09′56″N 85°20′34″E ~ 28°09′18″N 85°23′52″E, sweep-netting Urtica (prob.) dioica , 2 June 2006, T. Yasunaga, 2 ♁♁ 3 ♀♀ ( TYCN).
Differential diagnosis. Recognized by its chocolate brown general coloration; a distinct spine on posterior margin of episternum ( Fig. 50 View Figs 46–60 ); developed evaporative area widely occupying metathoracic scent efferent system ( Figs 51, 54 View Figs 46–60 ); dark femora with pale apices ( Figs 5–6 View Figs 1–6 ); unique shape of pygophore (with a bundle of remarkable spines as in Figs 19 View Figs 13–21 , 59 View Figs 46–60 , 64 View Figs 61–65 ); long flagellum of paramere ( Figs 59 View Figs 46–60 , 64 View Figs 61–65 ); and subapically inflated, gourd-like copulatory tube with a bottle-lid-shaped apex ( Figs 20 View Figs 13–21 , 65 View Figs 61–65 ). Externally similar to species of the subgenus Trichorius ; this new species can be distinguished by reduced corner seta at posterior angle of pronotum, presence of a spine on the episternum, developed evaporative area of the scent efferent system, and long flagellum of the paramere. Orius paveli is easily distinguished from O. (X.) miyamotoi Yasunaga, 1997 by the totally chocolate brown dorsum, reduced posterior corner setae on the pronotum and long flagellum of the paramere.
Description. Male. Macropterous. Body generally chocolate brown, oval and slightly elongate, small to moderate in size; dorsal surface moderately shining, with uniformly distributed pale, simple, semierect setae. Head shiny reddish brown, sometimes yellowish or paler brow in some specimens.Antenna dark brown, not thickened throughout; whole segment II and base of segment III yellow; segment II about 2/3 as long as head width across compound eyes; segment IV often tinged with red. Labium shiny reddish brown, reaching but not exceeding apex of procoxa. Pronotum shiny fuscous, sparsely and roughly punctate posterior to calli, with weak corner seta at anterior angle (posterior corner seta reduced); scutellum uniformly shiny dark brown, flat; pleura dark brown, partly reddish; posterior margin of episternum with spine ( Fig. 53 View Figs 46–60 ); metathoracic scent efferent system as in Figs 53–54 View Figs 46–60 , widely occupied by evaporative area. Hemelytron chocolate brown, weakly shining; membrane smoky brown. Coxae dark brown; legs pale brown; all femora dark brown, except for each apex yellowish brown; protibial teeth rather developed ( Fig. 55 View Figs 46–60 ); pretarsal structures as in Figs 56–57 View Figs 46–60 . Abdomen shiny chocolate brown. Male genitalia ( Figs 19 View Figs 13–21 , 58–60 View Figs 46–60 , 64 View Figs 61–65 ): Paramere disk-like, with folded process in middle, lacking denticule situated near base of flagellum ( Figs 28 View Figs 22–33 , 64 View Figs 61–65 ); conus tapered apically; flagellum very long, with thickened basal half.
Female. Macropterous. Similar in general coloration and shape to male; body ovoid, tumid; antenna slender and hemelytron not significantly infuscate. Female genitalia ( Figs 20 View Figs 13–21 , 65 View Figs 61–65 ): Copulatory tube subapically inflated, gourd-like, with bottle-lid-shaped apex.
Measurements (mm). Male (n = 4). Total length of body 1.66–1.68; head width across compound eyes 0.30–0.32; lengths of antennal segments I – 0.08–0.10, II – 0.21–0.23, III – 0.15–0.17, IV – 0.19–0.20; basal width of pronotum 0.67–0.69; maximum width across hemelytron 0.75–0.76; and lengths of metafemur 0.47–0.48, metatibia 0.51–0.56, and metatarsus 0.16–0.18.
Female (n = 3). Total length of body 1.50–1.62; head width across compound eyes 0.30–0.31; lengths of antennal segments I – 0.07–0.09, II – 0.19–0.20, III – 0.15–0.17, IV – 0.19–0.20; basal width of pronotum 0.66–0.74; maximum width across hemelytron 0.76–0.78; and lengths of metafemur 0.47–0.49, metatibia 0.48–0.51, and metatarsus 0.14–0.18.
Etymology. This new species is named in honor of the eminent Czech heteropterist, Prof. Pavel Štys, who regrettably passed away in August 2018; noun in genitive case standing in apposition.
Biology. This new species was confirmed to be associated with a stinging nettle, most similar to Urtica dioica L. ( Urticaceae ). Although its life cycle is unknown, Orius paveli was found on leaves and stems ( Fig. 10 View Figs 7–12 ) covered with stinging hairs (secreting formic acid) causing skin irritation (cf. YOSHIDA 2005), which presumably provides O. paveli a secure habitat. On the same plant, an unidentified species of thrips (Thysanoptera) co-occurred with the anthocorid which is assumed to prey on the thrips.
Comments. Subgeneric position of Orius paveli is currently not well elucidated, although at first sight it is reminiscent of a member of Trichorius . Nonetheless, the preponderance of the current evidence (i.e. the male genital segment bearing a bundle of strong spines on its dorsal surface [ Figs 19 View Figs 13–21 , 58–59 View Figs 46–60 , 63 View Figs 61–65 ] and similarity in shape of the female copulatory tube [ Figs 20 View Figs 13–21 , 65 View Figs 61–65 ]) argues in favor of the provisional placement of this new species in the subgenus Xylorius .
AMNH |
American Museum of Natural History |
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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