identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
156987DCFFF4FF925DC0F994FE5CFC6B.text	156987DCFFF4FF925DC0F994FE5CFC6B.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Xylota coquilletti Herve-Bazin 1914	<div><p>Xylota coquilletti Hervé-Bazin, 1914</p><p>(figs 1–2, 4)</p><p>Xylota cuprina Coquillett, 1898: 327, ♂ holotype, “No 3999 USNM”, “ Japan Mitsukuri”, [National Museum of Natural History, Washington DC], examined, nom. praeocc., nec Bigot (1885).</p><p>Xylota coquilletti Hervé-Bazin, 1914: 409, replacement name for Xylota cuprina Coquillett, 1898; Mutin &amp; Gilbert (1999: 50, fig. 3); Mutin &amp; Barkalov (1999: 492).</p><p>Xylota coquilletti amamiensis Shiraki, 1968: 122, ♂ holotype, “ V-15-1953 Ryukyu Is. T. Shiraki”, “ [ Zelima] coquilletti amamiensis v. nov . ♂ det. T. Shiraki” [National Institute for Agro-Environmental Sciences, Tsukuba, Japan], examined, syn. nov.</p><p>Xylota silvicola Mutin, 1988a: 103, ♂ holotype, «Ниж. Амур, р. Горин, верх. кл. Сиутару, 2.VII. [19]85, Мутин» (Russian Far East, Khabarovsky Krai, near Komsomolsk-na-Amure), [Zoological Institute, St. Petersburg], examined. Junior subjective synonym of Xylota cuprina Coquillett, 1898 according to Mutin &amp; Gilbert (1999); Mutin, 1988b: 121, the repeated description. Junior primary homonym and objective synonym of Xylota silvicola Mutin, 1988a .</p><p>Xylota huangshanensis He &amp; Chu, 1992: 6, figs 11–14, ♂ holotype, Anhui: Huangshan, [Shanghai Agricultural College], not examined. Junior subjective synonym of Xylota cuprina Coquillett, 1898 according to Mutin &amp; Gilbert (1999). Xylota vulgaris Yang &amp; Cheng in Cheng &amp; Yang, 1993: 330, figs 15–16, ♂ holotype, Guizhou: Huishui [Beijing Agricultural University], not examined, syn. nov.</p><p>Zelima coquilletti: Stackelberg, 1952: 320 (Zelima), part.</p><p>Remarks. When Coquillett (1898) described X. cuprina based on two males from Japan, he wrote in the original description that the “ type ” has the number 3999. The type specimens of X. cuprina were examined by Mutin in the National Museum of Natural History (Washington, DC). The holotype of X. cuprina (= X. coquilletti) with the label "No. 3999" has genitalia similar to those of the X. aeneimaculata species-group sensu Hippa (1978). The study of its genitalia established the synonymy of X. cuprina and X. silvicola (figs 1–2) with X. coquilletti . The description of X. silvicola was published twice (Mutin, 1988a, 1988b). Based on the male genitalia of X. huangshanensis He &amp; Chu, 1992, the latter can also be identified as a junior synonym of X. coquilletti (Mutin &amp; Gilbert 1999) . According to the figures of the male genitalia in the description of X. vulgaris Yang &amp; Cheng, 1993, this name should also be identified as a junior subjective synonym of X. coquilletti .</p><p>Examined material. Holotype of X. silvicola Mutin, ♂, RUSSIA: Khabarovsky Krai, lower reaches of Gorin river, the headwater of Siutaru stream, 2.VII.1985, leg. V. Mutin, [Zoological Institute of the Russian Academy of Sciences, St.-Petersburg, Russia (ZIN)]. Paratypes of X. silvicola Mutin: ♂, same data as holotype; ♂, Primorsky Krai, 30 km N from Terney, 13.VIII.1982, leg. V. Mutin, [Amurskii Humanitarian-Pedagogical State University (AmHPSU)]. Holotype of X. coquilletti amamiensis Shiraki, ♂, JAPAN: Ryukyu Is., Amami, Shinokawa, 15.V.1953, leg. T. Shiraki, [National Institute for Agro-Environmental Sciences, Tsukuba, Japan (NIAES)]. Other material: ♂, RUSSIA: Khabarovsky Krai, Myaochan mountains, 19.VIII.1996, leg. D. Gritskevich, [AmHPSU]; ♂, JAPAN: Honshu, Tottori Prefecture, Mt. Daisen, 6.VII.1966, leg. T. Okadome, [Institute of Systematics and Ecology of Animals, Novosibirsk, Russia (ISEA)].</p><p>Distribution. Russia: Primorsky Krai, southern part of Khabarovsky Krai; Japan: Hokkaido, Honshu, Ryukyu Islands; China (Guizhou).</p></div>	https://treatment.plazi.org/id/156987DCFFF4FF925DC0F994FE5CFC6B	Public Domain	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.		MagnoliaPress via Plazi	Mutin, Valerii;Ichige, Katsuyoshi	Mutin, Valerii, Ichige, Katsuyoshi (2014): A new species of Xylota Meigen (Diptera: Syrphidae) from the Far East. Zootaxa 3878 (2): 196-200, DOI: 10.11646/zootaxa.3878.2.6
156987DCFFF5FF905DC0FBBFFB58FA8E.text	156987DCFFF5FF905DC0FBBFFB58FA8E.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Xylota danieli Mutin & Ichige	<div><p>Xylota danieli Mutin &amp; Ichige spec. nov.</p><p>(figs 3, 5)</p><p>Xylota cuprina Coquillett, 1898: 327, ♂ paratype, “ Japan Mitsukuri” [National Museum of Natural History, Washington DC] examined. Note: The holotype and paratype of X. cuprina Coquillett belong to different species. Xylota coquilletti auct. nec Hervé-Bazin, 1914: Hippa, 1978: 71, fig. 32A; Stackelberg, 1952: 320 ( Zelima), part; Violovitsh, 1983: 143, fig. 221.</p><p>Xylota amamiensis auct. nec Shiraki, 1968: Mutin &amp; Gilbert, 1999: 47, new name for X. coquilletti sensu Hippa, 1978; Mutin &amp; Barkalov, 1999: 492.</p><p>Diagnosis. A new species similar to X. coquilletti and X. fo Hull, 1944 (which also inhabit East Asia) in having the metatibia with a basoventral range of setulae, but differing from the former by having an entirely pollinose frons, a rather uniformly pilose mesonotum and a thin, acute spike on the metatrochanter, as well as in features of the male genitalia. Xylota fo has a very long curved spike on the metatrochanter, a sharply concave apical fourth of tergum IV (lateral view), the metafemur with an anterior row of 12–14 strong setae and a posterior row of 9–10 strong setae and also differs in features of the male genitalia (Hippa 1978). The male genitalia of X. fo figured by Huo et al. (2007) belong to “ X. coquilletti ” in their sense.</p><p>Description. Male. Body length 8.2–10.5 mm, wing length 6–7 mm. Head. Face and frons entirely densely silverywhite pollinose. Vertex and occiput shining black dorsally, with bluish glow and scattered, erect white pile. Antenna brown, with darker basal 2 segments, basoflagellomere sometimes reddish ventrally. Eyes holoptic. Thorax. Postpronotum shining black laterally and dense white pollinose from within. Mesonotum shining back, with short, erect, pale pile. Scutellum shining black, pale pilose, sulcate, with long pale pile dorsoapically. Thorax more or less pollinose laterally, with denser pale pilosity on posterior anepisternum and katepisternum. Legs. Pro- and mesofemur mainly black except at the extreme apex, which is yellow, pale pilose. Pro- and mesotibia mainly yellow except for a more or less visible dark annulus at the middle. Pro- and mesotarsus mainly yellow except for the apical 2 tarsomeres, which are black. Metatrochanter with a short, thin, curved spike, its length shorter than the ventral setae on the metafemur. Metafemur black, mainly pale pilose except apical 1/6 with black pile, with an anterior row of 10–12 strong setae and a posterior row of 7–9 similar setae. Metatibia yellow on basal 2/5, with black setulae ventrally, and black on apical 3/5. Metatarsus entirely dark. Wing. Membrane hyaline, with brownish stigma; mainly microtrichose except for a small bare patch on the basal medial (bm) and posterior cubital (cup) cells, antero-basally. Abdomen. Visibly constricted in the middle, near connection between terga II and III. Tergum I usually black, tergum II black or dark brown, sometimes with a pair of diffuse reddish maculae; tergum III, as a rule, brown or reddish, usually paler basally; tergum IV brown or reddish, paler apically. Abdominal pile mainly pale except for areas of adpressed, very short, black pile on tergum II medially, tergum III postero-medially and tergum IV antero-medially. Sterna 7 and 8 pilose. Genitalia as in fig. 3. Female. Not reliably distinguishable from the related species X. fo.</p><p>Examined material. Holotype ♂, RUSSIA: Primorsky Krai, Bolshaya Ussurka river, Krutoy Yar village, 19.VI.1995, leg. V. Mutin, [Institute of Biology and Soil Science, Vladivostok, Russia (IBSS)]. Paratypes: RUSSIA: 11 ♂, same locality, 19–21.VI.1995, leg. V. Mutin, [6 ♂ IBSS; 5 ♂ Amurskii Humanitarian-Pedagogical State University (AmHPSU)]; 4 ♂, Primorsky Krai, 30 km N from Terney, Sichote-Alin reserve, 4.VIII.1982, leg. V. Mutin, [3 ♂ IBSS; ♂ AmHPSU]; ♂, Amurskaya Oblast, Malyi Khingan, Kundur, 19.VII.1988, leg. V. Makarkin, [IBSS]; ♂, Khabarovsky Krai, lower reaches of Gorin river, Tikhaya anabranch, 18.VI.1988, leg. V. Mutin, [AmHPSU], 4 ♂; Khabarovsky Krai, Pivan village, 19.–20.VI.1993, leg. V. Mutin, [AmHPSU]; ♂, same data except 20.VI.1992, [AmHPSU]; ♂, Bolshekhekhzyrsky reserve, environs of Bychikha village, 22.VI.1982, leg. V. Mutin, [AmHPSU]; ♂, Komsomolsk-na- Amure, Silinsky park, 31.VII.1996, leg. V. Mutin, [AmHPSU]; ♂, 25 km SW from Komsomolsk-na-Amure, environs of Molodezhny, 17.VII.1993, leg. V. Mutin, [AmHPSU]; JAPAN: 7♂, Hokkaido, Tomakomai C., Misawa, 21.VII.2006, leg. K. Ichige, [Katsuyoshi Ichige personal collection, (KIPC)]; ♂, Akita Pref., Ohmagari, 7.VI.1953, leg. N. Fukuhara, [National Institute for Agro-Environmental Sciences, Tsukuba, Japan (NIAES)]; ♂, Tochigi Pref., Nikko, 9.VIII.1953, leg. I. Hattori, [NIAES]; 2♂, Ibaraki Pref., Mt. Yamizo, 29.V.2007, leg. K. Ichige; 4♂, Ibaraki Pref., Gozen-yama, 2.V.2009, leg. K. Ichige, [KIPC]; ♂, Tokyo, Mt. Takao, 17.X.1965, leg. J. Minamikawa, [NIAES]; ♂, Gifu Pref., Takayama C., Hirayu, 3.VIII.2013, leg. K. Ichige, [KIPC]; ♂, Tokushima Pref., Mt. Nakatsumine, 20.VIII.1954, leg. M. Hirai, [NIAES]; ♂, Tsushima Is., Oboshiyama, 4.VIII.1974, leg. Y. Ikezaki, [NIAES]; 2 ♂, Ryukyu Is., Amami- Shinokawa, 11.V.1953, leg. T. Shiraki, [NIAES]; 2 ♂, Ryukyu Is., Amami-Oshima, Mt. Yuwan, 3.V.1953, leg. T. Shiraki, [NIAES].</p><p>Etymology. The specific name is dedicated to Daniel William Coquillett (1856–1911), the famous American dipterist.</p><p>Distribution. Russia: south of Khabarovsky Krai, Jewish Autonomous Oblast, south of Amurskaya Oblast, Primorsky Krai, Sakhalin Oblast, Japan: Hokkaido, Honshu, Shikoku, Kyushu, Ryukyu Islands.</p><p>Natural history. The larva is unknown. Feeding adults were observed on the inflorescences of Senecio cannabifolius; frequently adults collect pollen from the leaves of flowering plants. Males are associated with freshly sawn tree trunks. It is a common species of Xylota in the urban territories of the Russian Far East.</p></div>	https://treatment.plazi.org/id/156987DCFFF5FF905DC0FBBFFB58FA8E	Public Domain	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.		MagnoliaPress via Plazi	Mutin, Valerii;Ichige, Katsuyoshi	Mutin, Valerii, Ichige, Katsuyoshi (2014): A new species of Xylota Meigen (Diptera: Syrphidae) from the Far East. Zootaxa 3878 (2): 196-200, DOI: 10.11646/zootaxa.3878.2.6
