Aleochara (Triochara) trisulcata Weise, 1877
publication ID |
https://doi.org/ 10.5281/zenodo.282595 |
publication LSID |
lsid:zoobank.org:pub:F832C768-A8CA-4FEE-8C3B-BD933247FA6E |
DOI |
https://doi.org/10.5281/zenodo.6175380 |
persistent identifier |
https://treatment.plazi.org/id/03DE87D8-0832-FFD3-FF28-FB712CBE3BE6 |
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Plazi |
scientific name |
Aleochara (Triochara) trisulcata Weise, 1877 |
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Aleochara (Triochara) trisulcata Weise, 1877 View in CoL
( Figs. 53–56 View FIGURES 53 – 64 , 65–78 View FIGURES 65 – 70 View FIGURES 71 – 78 , 104 View FIGURES 104 – 105 )
Aleochara trisulcata Weise, 1877: 88 View in CoL (original description; type locality: “Hagi” [Hagi-shi, Yamaguchi-ken, western end of Honshû]); Lewis, 1879: 6 (catalogue of Japanese Coleoptera View in CoL ); Schönfeldt, 1887: 66 (catalogue of Japanese Coleoptera View in CoL ); Sawada, 1972: 39 (chaetotaxy of labial palpus), 40 (comments on pores of labial pulpus); Shibata, 1985: 321 (short description in Japanese; Coleoptera View in CoL of Japan), pl. 56 (habitus of specimen; misidentification of A. zerchei View in CoL ?); Naomi, S.I., 1989: 280 (checklist of Japanese Staphylinidae View in CoL ).
Aleochara (Triochara) trisulcata Weise, 1877 View in CoL ; Bernhauer, 1901b: 373 (establishement of subgenus); Fenyes, 1920: 414 (catalogue of world species of Aleocharinae View in CoL ); Scheerpeltz, 1925: 447 (catalogue of Palaearctic species of Aleocharinae View in CoL ); Bernhauer & Scheerpeltz, 1926: 795 (catalogue of world species of Aleocharinae View in CoL ); Adachi 1957: 34 (catalogue of Japanese species of Staphylinidae View in CoL ); Nakane, 1963: 100 (description in Japanese; Coleoptera View in CoL of Japan), pl. 50 (habitus of specimen; misidentification of A. zerchei View in CoL ?); Sawada, 1971: 312 (redescription); Sawada, 1972: table (character states, listed); Maus & Ashe, 1998c (online) (world checklist of subgenus); Cho & Ahn, 2001: 14, 31 (checklist of Korean Silphidae and Staphylinidae View in CoL ), 157(pl. 2) (habitus of specimen; misidentification of A. zerchei View in CoL ?); de Rougemont, 2001: 85 (record from Hong Kong); Park & Ahn, 2004: 195 (key to littoral species of genus Aleochara View in CoL in Korea), 196 (diagnosis; record from South Korea); Smetana, 2004: 358 (catalogue of Palaearctic species of Aleocharinae View in CoL ); Yamazaki, 2008: 152 (dipteran host record); Frank & Ahn, 2011: 20 (checklist of coastal Staphylinidae View in CoL of world); Yamazaki, 2012: 32 (ecological research).
Triochara trisulcata ( Weise, 1877) View in CoL ; Assing, 1995: 230 (diagonostic key to species of genus), 230 (redescription; lectotype designation).
Aleochara (Triochara) trisultata Weise, 1877 [misspelling]; Kuwayama, 1967: 138 (record from Kunashiri-tô; insect catalogue of southern Kuril Islands; misidentification of A. (T.) zerchei View in CoL or A. (T.) nubis View in CoL ?).
Type specimens. Not examined.
Non-type specimens. JAPAN: [Honshû]: 4 sex?, Benten-misaki (Sadoga-shima), Higashikowashimizu, Sado-shi, Niigata-ken (38.008N, 138.546E), 4 V 1998, Kinoshita-T. (cWat); 1 sex?, same data, but 5 V 1998, Tsuyuki-S. (cWat); 2 sex?, Ikarashi-hama, Ikarashi-2no-chô, Niigata-shi, Niigata-ken (37.871N, 138.927E), 29 V 1991, Hayashi-M. (sandy beach; cKaw); 1 3, Naga-hama, Nagai-2chôme 13, Yokosuka-shi, Kanagawa-Ken (35.191N, 139.615E), 7 IV 1975, Tao-M. (KUM); 1 sex?, Tsumeki-zaki, Shimoda-shi, Shizuoka-ken (34.659N, 138.987E), 21 IV 2003, Maruyama-M. (cMar); 2 sex?, Mukaiawagasaki, Uchinada-machi, Kahoku-gun, Ishikawaken (36.640N, 136.622E), 12 IV 1948, Takaba-S. (KUM); 2 sex?, Obama-shi, Fukui-ken (35.485N, 135.719E *), 6 VI 1980, Naomi-S.I. (KUM); 1 Ƥ, Maizuru, Kyôto-fu (35.514N, 135.387E *), 3 V 1980, Hayashi-Y. (cHayas); 1 sex?, river mouth of Onosato-gawa, Tarui, Sennan-shi, Ôsaka-fu (34.377N, 135.250E), 15 IV 2001, Kawakami-Y. (cKaw); 3 3, 24 sex?, Kugui, Higashi-ku, Okayama-shi, Okayama-ken (34.584N, 134.086E *), 31 III 2003, Fujitani-Y. (KUM); 2 Ƥ, 31 sex?, same data, but 9 V 2003 (under seaweed on beach); 18 sex?, same data, but 28 V 2003; 1 3, 11 sex?, Inazumi, Sugeura, Mihonoseki-chô, Matue-shi, Shimane-ken (35.564N, 133.166E *), 1-2 VI 2008, Hayama-T. (sandy beach; cHayam); 70 sex?, Konami-kaigan, Nonami, Shimane-chô, Matue-shi, Shimaneken (35.589N, 133.098E), 2-3 VI 2008, Hayama-T. (cHayam); 1 sex?, Koura-kaigan, Koura, Kashima-chô, Matueshi, Shimane-ken (35.520N, 132.975E), 16-18 VII 2009, Hayama-T. (FIT; cHayam); 47 sex?, Sotozono-kaigan, Sashiumi, Koryô-chô, Izumo-shi, Shimane-ken (35.333N, 132.664E), 8 III 2007, Hayama-T. (under seaweed; cHayam); 37 sex?, same data, but 12-13 IV 2009; 26 sex?, Kotoga-hama, Maji, Nima-chô, Ôda-shi, Shimane-ken (35.131N, 132.389E), 2 V 2009, Hayama-T. (YPT on supratidal zone; cHayam); 6 sex?, Kuromatsu-chô, Gôtsushi, Shimane-ken (35.057N, 132.310E), 2 V 2009, Hayama-T. (from seaweed; cHayam); 1 sex?, Iwami-kaigan, Kushiro-chô, Hamada-shi, Shimane-ken (34.955N, 132.127E), 16-17 VI 2008, Hayama-T. (YPT; cHayam); 1 sex?, Nagashima (Naga-shima), Kaminoseki-chô, Kumage-gun, Yamaguchi-ken (33.827N, 132.091E), 1 V 2008, Moriguchi-M. (KUM). [Shikoku]: 3 sex?, Ariake-hama, Muromoto-chô, Kanonji-shi, Kagawa-ken (34.139N, 133.642E), 9 IV 2011, Fujimoto-H. (sandy beach; KUM); 23 sex?, Iwagi (Akahone-jima), Kamijima-chô, Ochigun, Ehime-ken (34.234N, 133.159E *), 2 V 2009, Satô-Y. ( EEEU); 5 sex?, same data, but 7 V 2010, Senda-Y.; 2 3, 2 Ƥ, 2 sex?, Ôura, Matsuzaka-shi, Ehime-ken (33.996N, 132.771E), 15 IV 2010, Kawakami-Y. (cKaw). [Kyûshû]: 9 sex?, Watari, Fukutsu-shi, Fukuoka-ken (33.786N, 130.454E), 21 IV 2012, Yamamoto-S., Maruyama- M., Kanao-T. (from seaweed on small sandy beach with Aleochara (Emplenota) segregata ; KUM); 10 sex?, Watari, Fukutsu-shi, Fukuoka-ken (33.790N, 130.447E), 21 IV 2012, Yamamoto-S., Maruyama-M., Kanao-T. (from seaweed on huge sandy beach with A. (E.) segregata ; KUM); 2 sex?, Mitoma, Higashi-ku, Fukuoka-shi, Fukuoka-ken (33.703N, 130.417E), 3 VI 2001, Ogata-S. (KUM); 13 3, 23 sex?, Shimomaga-hama, Katsuma, Higashi-ku, Fukuoka-shi, Fukuoka-ken (33.684N, 130.290E), 15 V 2011 (11:30), Yamamoto-S. (seaweed on sandy beach with A. (E.) segregata ; cYam); 113 sex?, same data, but 21 III 2012; 2 sex?, Noko (Nokono-shima), Nishiku, Fukuoka-shi, Fukuoka-ken (33.608N, 130.299E), 20 III 2009, Yamamoto-S. (from a seaweed mass on sandy beach with A. (E.) segregata and A. (T.) zerchei ; cYam); 1 sex?, Takero-kaigan, Kayaki-machi, Nagasaki-shi, Nagasaki-ken (32.638N, 129.799E), 29 III 1992, Kusui-Y. (cItô); 2 sex?, Kin (Tsu-shima), Kamitsushima-chô, Tsushima-shi, Nagasaki-ken (34.568N, 129.469E), 5 V 2009, Yamamoto-S. (from decaying seaweed on sandy beach with A. (E.) fucicola ; cYam); 1 3, 3 Ƥ, 8 sex?, Higashimochida, Aira-chô, Aira-gun, Kagoshima-ken (31.724N, 130.640E *), 22 V 1984, Ôhara-M. (KUM). [Ryûkyû]: 1 3, 8 Ƥ, 5 sex?, Nakatane-chô (Tanega-shima), Kumage-gun, Kagoshima-ken (30.515N, 130.980E), 8-13 V 1996, Maruyama-M. (cMar); 1 Ƥ, Akaogi (Amami- Ôshima), Tatsugou-chô, Ôshima-gun, Kagoshima-ken (28.415N, 129.627E), 25 III 1978, Naomi-S.I. (KUM); 2 sex?, Kametsu (Tokuno-shima), Tokunoshima-chô, Ôshima-gun, Kagoshima-ken (27.716N, 129.018E *), 24 IV 1954, Kumata-T. (SCM); 2 sex?, China-chô (Okinoerabu-jima), Ôshima-gun, Kagoshima-ken (27.396N, 128.560E *), 24 III 1966, Itô-T. (cHayas).
Other specimens. [ JAPAN]: 1 sex?, Japan /Mus. Germ. [HW]// trisulcata We. [HW]/det. Bernhauer// Chicago NHMus/M. Bernhauer/Collection. [ FMNH]. [ CHINA, Hong Kong]: 1 male, Tai Long Wan, Lantau Island (22.220N, 113.884E *), 30 III 1997, de Rougemont G. M. ( BMNH); 1 sex?, Hong Kong /Waeken Coll/93-58 [HW]/ / China /Brit. Mus. [HW]// trisulcata /Wse. [HW]//Chicago NHMus/M. Bernhauer/Collection. [ FMNH].
Redescription. Body ( Fig. 53 View FIGURES 53 – 64 ): medium to somewhat large, normally medium sized; extremely robust and heavily sclerotized; very narrowly subparallel sided; entire body shining, but punctured areas of forebody, especially elytra, mat. Colour ( Figs. 53–56 View FIGURES 53 – 64 ): gland colour black to blackish brown with sometimes lighter colour in elytra; legs, especially tarsal segments, brown to reddish brown; maxillary and labial palpi reddish brown to brownish brown; antennae dark brown and partly reddish brown. Head ( Fig. 53 View FIGURES 53 – 64 ): longitudinal deep furrows on each side of midline, connected by deep transverse sulci at base. Antennae ( Fig. 65 View FIGURES 65 – 70 ): thick and quite robust; clearly shorter than combined length of head and pronotum; segment I, nearly 2.2 times as long as broad; segment II prominently shorter than I; segment III prominently shorter than II; segment IV normally spherical in certain angle; segments V to X strongly transverse; segment XI, about 1.3 times as long as broad; relative length (width) of segments from basal to apical: 10(4.5): 6.5(3): 4.5(3): 2(3): 2(4): 2(4): 2(4): 2(4.5): 2(4.5): 2(4.5): 6(4.5). Thorax: pronotum ( Figs. 53–54 View FIGURES 53 – 64 ) slightly wider than long (PW/PL =1.19), a little broader than head (PW/HW =1.26); surface blackishly shining without hexagonal reticulations and shallow distinct punctures, but some deep-distinct punctures and prominent longitudinal three furrows along midline forming three-dimensional patterns; impunctured areas largely similar to half-moon shape (without exception, and never cut into completely separated pieces; yellow coloured: Fig. 54 View FIGURES 53 – 64 ), surface of half-moon shining, and located at each side of midline; partly covered with short and thick brown-setae along furrows and deep punctures (white line: Fig. 54 View FIGURES 53 – 64 ); furrows of each side of midline slightly extended toward anterior (blue line: Fig. 54 View FIGURES 53 – 64 ). Inter coxal process of mesoventrite ( Figs. 55–56 View FIGURES 53 – 64 ) extremely sharp. Surface of mesoventrite ( Figs. 55–56 View FIGURES 53 – 64 ) rough. Inter coxal process of metaventrite ( Fig. 55 View FIGURES 53 – 64 ) triangular and pointed above. Legs ( Fig. 70 View FIGURES 65 – 70 ): hindtibia quite short, about 0.7 times as long as elytra (measured along midline); relative lengths of tarsomeres from basal to apical: 4: 3: 3: 3: 6 in foretarsus, 6: 4: 4: 4: 8 in midtarsus, 8: 5: 5: 5: 10 in hindtarsus. Abdomen: posterior margin of tergite VIII ( Figs. 71–72 View FIGURES 71 – 78 ), with a row of thick and short several sensory setae.
[Male]: posterior margin of tergite VIII ( Fig. 71 View FIGURES 71 – 78 ) nearly truncate, with around 8 macrosetae. Sternite VIII ( Fig. 73 View FIGURES 71 – 78 ) with about 4 macrosetae and around 5 thin macrosetae; posterior margin produced weakly and medially. Median lobe of aedeagus ( Figs. 75–76 View FIGURES 71 – 78 ) compactly elongated, moderately narrowed apically, elongated pyriform in ventral view ( Fig. 76 View FIGURES 71 – 78 ); a pair of circular subapico-ventral projections in lateral view ( Fig. 75 View FIGURES 71 – 78 ); apical lobe of median lobe extremely short-isosceles shape in ventral view ( Fig. 76 View FIGURES 71 – 78 ); flagellum shorter than the whole length of median lobe ( Figs. 75–76 View FIGURES 71 – 78 ).
[Female]: posterior margin of tergite VIII ( Fig. 72 View FIGURES 71 – 78 ) gently rounded or almost truncate, with around 7 macrosetae. Sternite VIII ( Fig. 74 View FIGURES 71 – 78 ) with 4 large macrosetae and around 3 thinner macrosetae; posterior margin moderately pointed and no big differences in compared with male. Spermatheca ( Fig. 78 View FIGURES 71 – 78 ): spermathecal head large, nearly twice longer than spermathecal stem (sa); spermathecal neck clearly shorter than (sa); basal portion of spermathecal stem distorted, with some bents.
Measurements (male: n=10): BL, 3.12–3.91 (3.62±0.24); FBL, 1.68–1.98 (1.84±0.09); HL, 0.45–0.62 (0.52±0.05); HW, 0.54–0.69 (0.63±0.04); AL, 0.74–0.91 (0.81±0.06); PL, 0.58–0.74 (0.68±0.05); PW, 0.68–0.86 (0.79±0.05); EL, 0.57–0.68 (0.62±0.03); EW, 0.82–0.99 (0.91±0.05); HTL, 0.37–0.54 (0.47±0.05).
Measurements (female: n=10): BL, 2.84–4.01 (3.34±0.42); FBL, 1.29–1.81 (1.62±0.17); HL, 0.38–0.51 (0.46±0.04); HW, 0.46–0.61 (0.55±0.05); AL, 0.59–0.83 (0.72±0.07); PL, 0.42–0.64 (0.58±0.07); PW, 0.55–0.79 (0.70±0.08); EL, 0.47–0.66 (0.58±0.06); EW, 0.66–0.89 (0.80±0.08); HTL, 0.27–0.48 (0.41±0.05).
Confirmed distribution by authors. [ JAPAN]: Honshû, Shikoku, Kyûshû, Ryûkyû, Sadoga-shima, Tsushima, Tanega-shima, Amami-Ôshima, Tokuno-shima, Okinoerabu-jima (See, Fig. 104 View FIGURES 104 – 105 for Japanese distribution); [ CHINA]: Hong Kong.
Other records in literature. [ SOUTH KOREA]: Chungnam Province, Jeonnam Province, Jeju Province ( Park & Ahn, 2004); [ RUSSIA]: Far East ( Ahn et al., 2000; no original citation; doubtful record).
Diagnosis. Aleochara trisulcata can be easily distinguished from the other Triochara species by a combination of the following character states: dorsal surface of head and pronotum shining; longitudinal subparallel furrows on head connected with a deep furrow at basal head (not shared character in A. nubis ); impunctured areas on pronotum similar to half-moon shape (never cut into completely separated pieces) and located at each side of midline (details in Fig. 54 View FIGURES 53 – 64 ); furrows on pronotum deep and prominent, never cut into pieces or wavy ( Fig. 54 View FIGURES 53 – 64 ); posterior margin of tergite VIII ( Figs. 71–72 View FIGURES 71 – 78 ) with a row of thick sensory setae (distinguishable character from A. zerchei and A. nubis ). [Male]: a pair of subapico-ventral projections on median lobe of aedeagus circular in lateral view ( Fig. 75 View FIGURES 71 – 78 ). [Female]: spermathecal stem (bs) ( Fig. 78 View FIGURES 71 – 78 ) moderately curved with some bents which is making somewhat similar to M-shape.
Remarks. This species is quite similar to A. zerchei , so that reconsideration of the records in the literature from Japan and adjacent regions is needed. For example, Ahn et al. (2000) recorded A. trisulcata with a short redescription and illustrations of genitalia of both sexes, however, this turned out to be a misidentification of A. zerchei by Park and Ahn (2004). In the latter paper, the presence of short longitudinal carina on tergite segments IV to V is mentioned as an important character state of A. trisulcata , but we could not confirm this character. They may have misidentified the character states or misjudged them.
Old records in Hokkaidô and the southern Kuril Islands are possibly misidentification of Aleochara (Triochara) zerchei and A. (T.) nubis . We did not confirm any specimen of true A. trisulcata in such regions.
Yamazaki (2008) recorded Fucellia apicalis Kertész, 1908 ( Diptera , Anthomyiidae ) as one of the host species of A. (T.) trisulcata and A. (E.) fucicola . Information on the parasitized months (April, May) is presented in Yamazaki (2012). Pupation takes place in the puparium of its host fly ( Yamazaki, 2008, 2012).
FMNH |
Field 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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Aleochara (Triochara) trisulcata Weise, 1877
Yamamoto, Shûhei & Maruyama, Munetoshi 2012 |
Triochara trisulcata (
Assing 1995: 230 |
Aleochara (Triochara) trisultata
Kuwayama 1967: 138 |
Aleochara (Triochara) trisulcata
Yamazaki 2012: 32 |
Frank 2011: 20 |
Yamazaki 2008: 152 |
Park 2004: 195 |
Smetana 2004: 358 |
Cho 2001: 14 |
Rougemont 2001: 85 |
Sawada 1971: 312 |
Nakane 1963: 100 |
Adachi 1957: 34 |
Bernhauer 1926: 795 |
Scheerpeltz 1925: 447 |
Bernhauer 1901: 373 |
Aleochara trisulcata
Naomi 1989: 280 |
Shibata 1985: 321 |
Sawada 1972: 39 |
Schonfeldt 1887: 66 |
Lewis 1879: 6 |
Weise 1877: 88 |