Higher resolution figure plates of "Revision of the subgenus Coprochara Mulsant & Rey of the genus Aleochara Gravenhorst from Japan (Coleoptera: Staphylinidae: Aleocharinae)"

Accepted by J. Klimaszewski: 5 Mar. 2013; published: 24 Apr. 2013 Licensed under a Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0 ZOOTAXA ISSN 1175-5326 (print edition) ISSN 1175-5334 (online edition) Copyright © 2013 Magnolia Press Zootaxa 3641 (3): 201–222 www.mapress.com / zootaxa / Article 201 http://dx.doi.org/10.11646/zootaxa.3641.3.1 http://zoobank.org/urn:lsid:zoobank.org:pub:8E36BE56-61EA-4FB9-BEF8-BCDA043EA6DE Revision of the Subgenus Coprochara Mulsant & Rey of the Genus Aleochara Gravenhorst from Japan (Coleoptera: Staphylinidae: Aleocharinae) SHÛHEI YAMAMOTO1, 2 & MUNETOSHI MARUYAMA2 1Entomological Laboratory, Graduate School of Bioresource and Bioenvironmental Sciences, Kyushu University, Hakozaki 6-10-1, Fukuoka, 812-8581 Japan. E-mail: [email protected] 2The Kyushu University Museum, Hakozaki 6-10-1, Fukuoka, 812-8581 Japan Abstract A taxonomic revision of the subgenus Coprochara Mulsant & Rey, 1874 of the genus Aleochara Gravenhorst, 1802 in Japan is presented. The following three species are recognized: Aleochara (C.) verna Say, 1833, A. (C.) binotata Kraatz, 1856 and A. (C.) squalithorax Sharp, 1888, of which A. binotata is new to Japan. All previous records of “A. (C.) bipustulata (Linnaeus, 1760)” should be regarded as misidentifications of either A. verna or A. binotata. New records are added for, A. squalithorax, a littoral species. All species are redescribed, figured, keyed and mapped. Key words: Aleocharini, biodiversity, identification key, redescription, rove beetle, taxonomy Introduction The rove beetle genus Aleochara Gravenhorst, 1802 is a large group in Aleocharinae, comprising more than 450 species in 19 subgenera (Park & Ahn, 2010; Yamamoto & Maruyama, 2012). Aleochara is distributed throughout the world, except for Antarctica (Klimaszewski, 1984; Maus et al., 2001). Aleochara is one of the taxonomically difficult groups in Coleoptera. The genus includes many large adults and commonly found species of Aleocharinae; thus, precise and simpler identification methods are required. Close similarities in external and internal structures, and cosmopolitan distributions of several species make species identification difficult. Larvae of Aleochara are known to be parasitoids of cyclorrhaphous Diptera, and some species, especially members of the subgenus Coprochara Mulsant & Rey, 1874, are expected to be biological control agents of notorious pest flies (e.g., Klimaszewski & Jansen, 1993, 1994; Maus et al., 1998, 2001; Fournet et al., 2000). Thus, most Aleochara species typically occur in fly-infested habitats such as animal droppings, decaying plant material, and carrion (Klimaszweski, 1984; Yamamoto & Maruyama, 2009, 2012). Aleochara species in Asia are far from adequately described, and taxonomic knowledge of Japanese Aleochara is still incomplete; only 25 species have been recorded (Bernhauer & Scheerpeltz, 1926; Smetana, 2004; Yamamoto & Maruyama, 2009, 2012). The species of Coprochara have been problematic even in Europe and North America, and to date, no one has conducted a taxonomic review of the Japanese species of the subgenus. The purpose of this study, the third series of contributions to the Japanese Aleochara fauna, is to clarify the taxonomic identity of Japanese Coprochara species and to investigate geographical variation within each species. All three species are redescribed with diagnosis and figures. Diagnostic keys and distribution maps are also provided. Figures showing collection sites for two species are included. YAMAMOTO & MARUYAMA 202 · Zootaxa 3641 (3) © 2013 Magnolia Press Materials and methods Deposition of materials Approximately 700 dry specimens of adult individuals were examined. Most of the material is deposited in the following public institutions and private collections. Institutions: BMNH The Natural History Museum, London, UK (R. Booth). CBM The Natural History Museum and Institute, Chiba, Japan (A. Saitô). KUM The Kyushu University Museum, Fukuoka, Japan (S.-I. Naomi & S. Nomura Rove Beetle Collection, and M. Maruyama Collection) (M. Maruyama). SCM The Sagamihara City Museum, Kanagawa, Japan (H. Moriya). Private collections: cHaga Kaoru Haga (Tôkyô, Japan). cHay Yasuhiko Hayashi (Hyôgo, Japan). cIto Tateo Itô (Kyôto, Japan). cOno Hiroki Ono (Chiba, Japan). cShi Yasutoshi Shibata (Tôkyô, Japan). cWat Takashi Watanabe (Kanagawa, Japan). cWatY Yasuaki Watanabe (Tôkyô, Japan). cYam Shûhei Yamamoto (Fukuoka, Japan). Measurements and terminology The technical procedures, terminology, and other methods adopted here were given in detail in Maruyama (2006) and Yamamoto and Maruyama (2012). Words for genital parts were adopted mainly from Welch (1997) and Maus (1998). The specimen data used in this study largely did not follow the original spellings and place names written on specimen labels. We corrected for more precise and detailed information, except for some type materials. The original spellings on the label attached to the specimen were adopted in such cases (after Yamamoto & Maruyama, 2012). Abbreviations for morphology and materials Genital structures are abbreviated as follows: ai, apical invagination of spermatheca; bs, basal swelling of median lobe; sa, apical portion of spermathecal stem; sb, basal portion of spermathecal stem; sga, attachment of spermathecal duct; sh, head of spermatheca; sm, membranous portion of spermathecal duct; and sn, neck of spermatheca (after Welch, 1997: Figs. 1, 4; see Figs. 18, 21, 29 in the present paper). Conditions of specimen labels are abbreviated as follows: HW, hand written; PC, paper card; PRL, purple round label pinned by a curator; RRL, red round label pinned by a curator. Elytral color variations in Aleochara squalithorax are abbreviated as follows: GT, gray type; YT, yellow type. Glossary of Japanese local names Japanese place names generally follow the same spelling used in Japan except for some English nouns. Words nearly correspond as follows: -mura (village); -chô, -machi (town); -ku (ward/district); -shi (city); -gun (county); - to, -fu, -ken (prefecture); -dake, -take, -san, -zan, -yama (mountain); -misaki, -zaki (cape); -gawa (river, stream); - kaigan, -hama (seashore beach); -shima (island); -shotô (islands, archipelago). Zootaxa 3641 (3) © 2013 Magnolia Press · 203 TAXA/RUNNING TITLE 8 PT IN UPPER CASE FIGURES 1–4. Japanese species of Aleochara (Coprochara) in habitus. 1. Aleochara (Coprochara) verna; 2. A. (C.) binotata; 3–4. A. (C.) squalithorax: gray type (Fig. 3) and yellow type (Fig. 4). YAMAMOTO & MARUYAMA 204 · Zootaxa 3641 (3) © 2013 Magnolia Press FIGURES 5–13. Japanese species of Aleochara (Coprochara). 5–7. Aleochara (Coprochara) verna; 8–10. A. (C.) binotata; 11–13. A. (C.) squalithorax. (5, 8, 11: elytra; 6, 9, 12: intercoxal process of metaventrite; 7, 10, 13: mesoventrite and metaventrite). Systematics Genus Aleochara Gravenhorst, 1802 See Klimaszewski (1984), Smetana (2004), and Gouix and Klimaszewski (2007) for synonymic information and references. A detailed description is provided by Klimaszewski (1984) and a short description is provided by Yamamoto and Maruyama (2012). Subgenus Coprochara Mulsant & Rey, 1874 Coprochara Mulsant & Rey, 1874: 146; Klimaszewski, 1984: 14; Lohse, 1989: 236; Klimaszewski & Jansen, 1994: 148; Welch, 1997: 3; Maus, 1998: 83; Maus & Ashe, 1998 (online); Klimaszewski et al., 2000: 237; Smetana, 2004: 355; Gouix & Klimaszewski, 2007: 23. Baryodma Thomson, 1858: 31. Eucharina Casey, 1906: 165. [homonym]. Funda Blackwelder, 1952: 166. [replacement name]. Mecorhopalus Solier, 1849: 347. Skenochara Bernhauer & Scheerpeltz, 1926: 795. See Klimaszewski (1984) and Maus (1998) for further references. Type species: Aleochara bilineata Gyllenhal, 1810. Zootaxa 3641 (3) © 2013 Magnolia Press · 205 TAXA/RUNNING TITLE 8 PT IN UPPER CASE Diagnosis. The subgenus Coprochara can be distinguished from the other subgenera of Aleochara by the combination of following character states (see details in Klimaszewski, 1984; Klimaszewski & Jansen, 1994; Maus, 1998): antennae thick with segments V–X clearly transverse; two longitudinal, parallel or subparallel rows of more or less impressed punctures on midline of pronotum; elytra in some species with orange or yellow spot; mesoventrite with complete carina; spermatheca usually multiply coiled posteriorly, varying from 1 to more than 100 coils; median lobe of aedeagus with flagellum and distinctively arranged sclerites (Figs. 18–19), lacking subapico-ventral projections (see Yamamoto & Maruyama, 2012: Fig. 18). Remarks. The subgenus Coprochara includes 37 species worldwide and 18 species from the Palearctic region (Maus, 1998, 2000; Smetana, 2004). This subgenus is widely distributed in all zoogeographical regions (Klimaszewski, 1984). The taxonomy of the subgenus Coprochara is difficult due to external similarity, considerable variation within species, and incorrect interpretations of the configuration of male genitalia (Maus, 1998). For example, species identifications in England were confused until the late 1980s (Welch, 1990, 1997). Despite these taxonomic difficulties, species belonging to the subgenus have attracted special attentions as biological control agents for pest flies. Most studies on the subgenus have used A. (C.) bilineata Gyllenhal, 1810, A. (C.) bipustulata (Linnaeus, 1760), and A. (C.) verna Say, 1833. One advantage of using the subgenus Coprochara for biological control is that they are native species within a wide distribution range, which reduces ecological impact on ecosystems. Phylogenetic relationships among species of the subgenus Coprochara are relatively well known. Maus and Ashe (1998), based on morphological characters, and Maus et al. (2001), based on molecular data, produced phylogenetic trees for the subgenus. However, Maus and Ashe (1998) noted difficulties in the examination of phylogenetic relationships within the subgenus, such as the high frequencies of parallelism and homoplasy in the group, and most of the apomorphic character states have evolved independently in different lineages within the subgenus. Three species of the subgenus Coprochara have been recorded in Japan, A. bipustulata, A. squalithorax Sharp, 1888, and A. verna, the latter reliably only from Gunma and Kanagawa Prefectures (Maus, 1998; Park et al., 2011). “Aleochara bipustulata”, on the other hand, has been widely recorded from Japan. The littoral species, A. squalithorax was originally described from Hokkaidô and Honshû (Sharp, 1888). Key to species from the subgenus Coprochara in Japan 1. Body (Figs. 3–4) gray, thick, spindle shaped; dorsal surface covered with granular microstructures and forebody not glossy at all. Intercoxal process of metaventrite (Figs. 12–13) narrow and long, pointed apically. Elytra (Fig. 11) with posterior margins deeply notched laterally; surface rough, densely covered with short but robust setae. Tergite VIII (Figs. 34–35) with numerous large oval projections on surface. Collected from decaying seaweed on seashore beach. [Male]: median lobe of aedeagus as in Figs. 38–39; sclerite Z large, without attachment at apex; flagellum longer than median lobe of aedeagus. [Female]: proximal portion of spermatheca (Fig. 41) with extremely numerous coils. . . . . . . . Aleochara (Coprochara) squalithorax Sharp, 1888 - Body black to blackish brown, slender, parallel or subparallel sided; dorsal surface not covered with granular microstructures, and clearly glossy. Intercoxal process of metaventrite wide and rounded apically. Elytra with posterior margins rounded, usually with yellowish portion. Tergite VIII without large oval spines on surface, with serrate or truncate posterior margin. Spermatheca proximally with 20 coils at most . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 2. Dorsal surface smooth and apparently glossy (Fig. 1). Pronotum with shallow and inconspicuous punctures and with thin setae. Two rows of punctures along midline fine. Elytra (Fig. 5) with a pair of small reddish to yellowish spots near posterior margin and suture, bearing with numerous thin and inconspicuous setae. Common species in Japan. [Male]: sternite VIII (Fig. 16) simple and weakly pointed. Median lobe of aedeagus (Figs. 18–19): apex of apical lobe of median lobe blunt in lateral view; flagellum long, slightly longer than median lobe of aedeagus; sclerite Z large, with long and prominent attachment, waving toward apex. [Female]: coiled portion of spermatheca (Fig. 21) not greatly extended laterally.. . . . . . . A. (C.) verna Say, 1833 - Body more slender. Elytra entirely yellow except for anterior margins near pronotum (Japanese specimens). . . . . . . . . . . . . .3 3 Dorsal surface with distinct and deep coarse punctures, and with thick yellowish setae (Fig. 2). Pronotum with distinct punctures and rows of deep punctures along midline. [Male]: sternite VIII (Fig. 24) pointed triangularly. Median lobe of aedeagus (Figs. 26–27): apex of apical lobe sharply pointed in lateral view; flagellum short, but basal plate of flagellum long and large; sclerite Z small, with straight attachment pointed toward apex. In Japan known only from Hokkaidô. [Female]: proximal portion of spermatheca (Fig. 29) with thick coils and widely extended laterally. . . . . . . . . . . . . . . . . A. (C.) binotata Kraatz, 1856 YAMAMOTO & MARUYAMA 206 · Zootaxa 3641 (3) © 2013 Magnolia Press FIGURES 14–21. Terminalia of Aleochara (Coprochara) verna. 14. tergite VIII of male; 15. tergite VIII of female; 16. sternite VIII of male; 17. sternite VIII of female; 18. male genitalia: median lobe of aedeagus in lateral view; 19. male genitalia: median lobe of aedeagus in ventral view; 20. apical lobe of paramerite, lateral view; 21. female genitalia: spermatheca. Zootaxa 3641 (3) © 2013 Magnolia Press · 207 TAXA/RUNNING TITLE 8 PT IN UPPER CASE FIGURES 22–29. Terminalia of Aleochara (Coprochara) binotata. 22. tergite VIII of male; 23. tergite VIII of female; 24. sternite VIII of male; 25. sternite VIII of female; 26. male genitalia: median lobe of aedeagus in lateral view; 27. male genitalia: median lobe of aedeagus in ventral view; 28. apical lobe of paramerite, lateral view; 29. female genitalia: spermatheca. YAMAMOTO & MARUYAMA 208 · Zootaxa 3641 (3) © 2013 Magnolia Press FIGURES 30–33. Mouth parts of Aleochara (Coprochara) squalithorax of male. 30. labium; 31. maxilla; 32. labrum; 33. mentum. Zootaxa 3641 (3) © 2013 Magnolia Press · 209 TAXA/RUNNING TITLE 8 PT IN UPPER CASE FIGURES 34–41. Terminalia of Aleochara (Coprochara) squalithorax. 34. tergite VIII of male; 35. tergite VIII of female; 36. sternite VIII of male; 37. sternite VIII of female; 38. male genitalia: median lobe of aedeagus in lateral view; 39. male genitalia: median lobe of aedeagus in ventral view; 40. apical lobe of paramerite, lateral view; 41. female genitalia: spermatheca. YAMAMOTO & MARUYAMA 216 · Zootaxa 3641 (3) © 2013 Magnolia Press Matsue-shi, Shimane-ken, 17. VII. 2010, S. Yamamoto leg. (under dry flotsam on sandy beach; cYam); 1 ♂ (GT), 1 ♀ (GT), 5 sex? (GT), Taki-chô, Hikawa-gun, Shimane-ken, 2. VI. 1980, S.-I. Naomi leg. (KUM). [Kyûshû]: 5 ♂♂ (GT), 1 ♂ (YT), 2 ♀♀ (GT), 1 ♀ (YT), 122 sex? (GT), 17 sex? (YT), Watari, Fukutsu-shi, Fukuoka-ken, 21. IV. 2012, S. Yamamoto, M. Maruyama, T. Kanao leg. (from dry to wet seaweed on huge sandy beach; KUM); 5 sex? (GT), 3 sex? (YT), Watari, Fukutsu-shi, Fukuoka-ken, 21. IV. 2012, S. Yamamoto, M. Maruyama, T. Kanao leg. (from dry to wet seaweed on small sandy beach; KUM); 1 ♂ (YT), 1 ♀ (YT), 4 sex? (GT), 1 sex? (YT), Mitoma, Higashi-ku, Fukuoka-shi, Fukuoka-ken, 3. VI. 2001, S. Ogata leg. (KUM); 2 sex? (GT), Katsuma (Shikano-shima), Higashi-ku, Fukuoka-shi, Fukuoka-ken, 21. III. 2012, S. Yamamoto leg. (from seaweed on huge sandy beach; cYam); 1 sex? (GT), Karatsu-shi, Saga-ken, 7. VII. 1975, H. Ohishi leg. (KUM); 2 sex? (GT), Minamiôsumi-chô (Sata-misaki), Kimotsuki-gun, Kagoshima-ken, 28. V. 1958, Y. Miyake leg. (cHay); 1 ♀ (GT), 11 sex? (GT), Nakatane-chô (Tanega-shima), Kumage-gun, Kagoshima-ken, 8-13. V. 1996, M. Maruyama leg. (KUM). Redescription. Body (Figs. 3–4): thick and spindle shaped, especially for small individuals (Fig. 4), small to medium sized, ca. 3.48 mm in body length (3.14–3.83 mm, N = 15), and 1.88 mm in fore body length (1.68–2.15 mm, N = 15), normally moderate in size; entire body heavily robust; dorsal surface mat; forebody covered with granular microstructures. Color (Figs. 3–4, 11–13): ground color gray to blackish brown; legs, especially tarsal segments, and mouth parts dark brown to reddish brown; elytra gray in most cases as Fig. 3, but some individuals with huge yellowish portion except for anterior and lateral margins as Fig. 4; antennae reddish brown to dark brown, surface densely pubescent with minute yellowish setae. Head (Figs. 3–4): circular (head length = 0.42–0.56 mm (mean = 0.48 mm), head width = 0.46–0.56 mm (mean = 0.51 mm), N = 15), slightly transverse (head width / head length = 1.08 (mean), N = 15), widest at eyes; surface entirely covered with hexagonal reticulations, lacking punctation, but covered with short and thick setae sparsely. Antennae (Figs. 3–4): moniliform, robust and thickened apically, slightly longer than head length (antenna length = 0.57–0.84 mm (mean = 0.73 mm), N = 15); segment I, about 2.1 times as long as broad, segment II slightly shorter than I, segment III apparently shorter than II, segments IV to VI more or less spherical, as long as width except for stem of each segment, segment VII moderately wider than long, segments VIII to IX clearly transverse, segment X strongly transverse, segment XI thick and conical, nearly 1.2 times as long as width, as same length as segment I, approximate relative length of segments from basal to apex: 10.5: 10.0: 6.0: 4.5: 4.5: 4.5: 4.5: 4.5: 4.5: 4.5: 10.5. Mouth parts (Figs. 30–33): mandibles slightly asymmetric, left one with one tooth near apex. Clypeus rounded apically. Labrum (Fig. 32) transverse, about 1.3 times as wide as long, anterior margin slightly emarginated medially, basal half semitransparent, apodeme roundly produced postero-medially; surface with numerous pseudopores scattered randomly in apical part. Ligula (Fig. 30) bilobed, with each lobe rounded apically. Labial palpus (Fig. 30) with segment I thicker and longer than II, segment II weakly dialated, segment III shorter than II. Mentum (Fig. 33) nearly trapezoidal, much wider than long, about 2.0 times as wide as long; anterior margin strongly emarginated; entire surface with numerous pseudopores scattered randomly. Maxilla (Fig. 31): maxillary palpus with thick and long segment II and III, segment II as long as III, segment IV short, less than half length of segment III; galea thick and short, clearly shorter than segment II of maxillary palpus; lacinia with numerous setae and with dozens of thick spines pectinately. Thorax: pronotum (Figs. 3–4) transverse (pronotum length = 0.60–0.76 mm (mean 0.69 mm), pronotum width = 0.77–0.94 mm (mean = 0.88 mm), pronotum width / pronotum length = 1.27 (mean), N = 15), clearly wider than head (pronotum width / head width = 1.71 (mean), N = 15), widest around basal 1/3, weakly narrowing apically; surface uniformly covered with large hexagonal reticulations, thick-short setae but without distinct punctation; midline longitudinally elevated weakly above, glabrous, lacking punctation. Intercoxal process of mesoventrite (Fig. 13) with strongly developed carina along midline. Intercoxal process of metaventrite (Figs. 12–13) narrow and long, apparently pointed apically. Metaventrite (Fig. 13) rough, densely pubescent like elytra. Elytra (Figs. 3–4, 11) wider than long (elytra length = 0.62–0.78 mm (mean = 0.68 mm), elytra width = 0.90–1.13 mm (mean = 1.04 mm), N = 15), rugose, moderately covered with yellowish thick and short setae; posterior margins deeply notched laterally (Fig. 11); [Gray type]: dorsal surface entirely gray, but [Yellow type]: with a pair of large yellowish portions, extending from apical to posterior except for anterior margins and shoulders close to pronotum as well as lateral margins of elytra and elytral suture (posterior margins colored). Legs (Figs. 3–4): short (hind tibia length = 0.49–0.65 mm (mean = 0.57 mm), N = 15) and thick, dozens of thick spines on tibia, especially on fore and midtibia; relative lengths of tarsal segments from basal to apical: 5.0: 3.5: 3.5: 3.0: 8.0 in foretarsus, 8.0: 5.0: 5.0: 4.5: 14.5 in midtarsus, 17.5: 10.0: 7.0: 7.0: 14.5 in hindtarsus. Abdomen (Figs. 3–4): rogose, except for anterior margin of each tergite and posterior margin of tergite VI to VII; tergite VIII (Figs. 34–35) with dozens of thick spines scattered in posterior half. Zootaxa 3641 (3) © 2013 Magnolia Press · 217 TAXA/RUNNING TITLE 8 PT IN UPPER CASE [Male]: posterior margin of tergite VIII (Fig. 34) rounded, with approximately 7 macrosetae on each side. Sternite VIII (Fig. 36) with one macroseta (difficult to identify); posterior margin weakly pointed. Median lobe of aedeagus as in Figs. 38–39: compactly elongated and narrowed toward apex; flagellum long, clearly longer than median lobe of aedeagus; sclerite Y large; sclerite Z large without attachment at apex; apical lobe in lateral view slightly bent, narrowing subapically, median lobe in ventral view elongated, weakly narrowing toward apex; basal swelling of median lobe large and oval; apical lobe looks short isosceles. Apical lobe of paramerite (Fig. 40) short and thick, widest at subapical portion, bearing 4 setae. [Female]: tergite VIII (Fig. 35) with rounded posterior margin like male, with approximately 4 macrosetae. Posterior margin of sternite VIII (Fig. 37) weakly pointed, with one macroseta (difficult to confirm). Spermatheca (Fig. 41): apical invagination of spermatheca tiny and shallow; spermathecal head fused with spermathecal neck; attachment of spermathecal duct prominent; (sn) short, slightly narrowing toward basal portion of spermathecal stem; coiled portion extremely long, composed with countless times of moderately thick coils, not extended laterally, waving toward membranous portion of spermathecal duct; coils directly connected with thick (sm); each part of spermatheca except for (sm) entirely and strongly sclerotized; inner wall of (sh) coarsely and that of (sb) in apical portion also coarsely striate with rough mesh striate in mid to posterior part of (sb). Diagnosis. Aleochara squalithorax can be easily distinguished from the other Coprochara in Japan by a combination of the following character states: body thick and spindle shaped; surface mat with granular microstructures, covered with thick and short setae coarsely but without punctation on head and pronotum (Figs. 3– 4); pronotum clearly wider than head, without rows of punctures along midline; elytra with posterior margin deeply notched, sometimes with yellowish portion on dorsal surface (YT: Figs. 4, 11); intercoxal process of metaventrite narrow and sharply pointed apically (Fig. 13); tergite and sternite VIII with thick spines in posterior half (Figs. 34– 35). [Male]: flagellum long; sclerite Z large without attachment (Figs. 38–39); apical lobe of paramerite short, thick, without numerous minute setae (Fig. 40). [Female]: countless coiled portion with spermatheca (Fig. 41). Confirmed distribution by the present study. [JAPAN]: Hokkaidô, Honshû, Kyûshû, Tanega-shima. Other localities in the literature. [EAST ASIA]: South Korea (Ahn et al., 2000; Park & Ahn, 2004). Remarks. Aleochara squalithorax is a rather common species in Japan but has a limited distribution globally. Until now, this taxon has only been recorded from Japan and South Korea (Smetana, 2004; Frank & Ahn, 2011). A recent study provided the first record of A. squalithorax from South Korea and briefly redescribed the species and provided a figure of the median lobe of the aedeagus of the male, based on Korean specimens (Ahn et al., 2000). The distribution of A. squalithorax in Japan is wide, from northeastern Hokkaidô (Nemuro) to southwestern Kyûshû (Tanega-shima). We provide new distributional records from mainland Kyûshû. This species is considered a highly derived taxon of the subgenus Coprochara and it has attracted special attention from researchers (Bernhauer & Scheerpeltz, 1926; Assing, 1995; Maus, 1998). Thus, the line drawings of mouth parts, which are important characters in Aleocharinae that have never been described, are also provided in this paper. Historical notes. This species was originally described as “Aleochara squalithorax” from “Hagi [Hagi-shi, western end of Honshû, Japan] (Fauvel), Hakodate [Hakodate-shi, Hokkaidô, Japan] (Lewis)” by Sharp (1888). Afterward, Fenyes (1920) included it within the peculiar subgenus Eucharina Casey, 1906. A few years later, Bernhauer and Scheerpeltz (1926) transferred A. squalithorax to the newly established subgenus Skenochara Bernhauer & Scheerpeltz, 1926 as the type species, and it was the only species assigned to Skenochara. Assing (1995) raised this subgenus to generic rank (still only one species remained in the taxon). This paper was especially important because A. squalithorax was redescribed with figures and the male lectotype was designated. The systematic position of Skenochara was unclear, although Assing (1995) tentatively treated it as a distinct genus. Maus and Ashe (1998) and Maus (1998) detected Skenochara with all apomorphies that characterize the subgenus Coprochara; i.e., the existence of dorsal longitudinal rows on the pronotum, a strongly coiled spermatheca in the female, and a completely carinate mesoventrite. Therefore, Skenochara was synonymized under the subgenus Coprochara by Maus (1998). In addition to morphological evidence, molecular information supported this treatment (Maus et al., 2001; see Phylogeny of A. squalithorax). Bionomics. SY and MM collected the species at several different locations in Hokkaidô, Honshû and Kyûshû that faced both the Pacific Coast and the Sea of Japan (Fig. 45). All of the locations were sandy beaches, none of the areas were very small, and they generally had good environmental conditions (Fig. 43). Individuals were found from completely dry seaweed masses on beaches that were far from the shoreline from sites that were and close to YAMAMOTO & MARUYAMA 218 · Zootaxa 3641 (3) © 2013 Magnolia Press coastal vegetation at Hamamatsu and Urayakotan in Hokkaidô; specimens were also collected from somewhat wet seaweed at Watari, Kyûshû (Fig. 43). Adults were observed and collected from early spring (March) to mid-fall (October), with the highest number of individuals being observed between April and May. Host records. No information is available for A. squalithorax. Phylogeny. Phylogenetic trees in Maus et al. (2001) show relationships among A. verna, A. binotata, and A. squalithorax. All three species were included in the Coprochara clade. Aleochara squalithorax formed a sister group with littoral A. (C.) sulcicollis Mannerheim, 1843 from North America. Microsculpture is present in Emplenota, Maseochara, Polystomota, and A. squalithorax, but none of the analyses supported a monophyletic clade of these taxa (Maus et al., 2001). Color variation in elytra. Two patterns of elytral color variation were found. The gray type (Fig. 3) is apparently the typical form and the yellow type (Figs. 4, 11) is much rarer. We examined both types morphologically, but no differences were found between the two types. Thus, the authors concluded that the difference represents color variation within A. squalithorax. The yellow type accounted for only 12.6% of the total number of individuals collected (N=470). The ratio also showed considerable variation among locations. For example, no yellow-type individuals were found among 55 specimens at Sanriga-hama in Hokkaidô. In contrast, the yellow type accounted for 14.1% in Watari (data combined across small and large beaches), Kyûshû (N=156), and the highest ratio, 45.9%, was recorded in Katsuura, Honshû (N=37). FIGURES 42–43. Habitats of the subgenus Coprochara of the genus Aleochara in Japan. 93. the summit of Sobo-san (located in boundaries between Ôita and Miyazaki Prefectures; only observed; A. (C.) verna: arrow); 43. Watari (Fukutsu, Fukuoka Prefecture; A. (C.) squalithorax: arrow). Discussion Does Aleochara bipustulata occur in Japan? As a yellow-spotted Aleochara species, Aleochara (Coprochara) bipustulata (Linnaeus, 1760) was thought to be a very common species in Japan. The first record of A. bipustulata in Japan was given by Sharp (1888) as A. nitida Gravenhorst, 1802, which was later synonymized under A. bipustulata. Adachi (1957) recognized A. bipustulata in his catalog of Japanese rove beetles. Naomi (1989) and Smetana (2004) followed this treatment. However, we examined more than 250 Japanese specimens that have hitherto been identified as A. bipustulata, and no specimen of A. bipustulata was found. These specimens were identified as A. verna Say, 1833 or A. binotata Kraatz, 1856. In conclusion, we exclude A. bipustulata from the Japanese insect fauna. The confusions of A. bipustulata in North America addressed in Hemachandra et al. (2005) and addressed in Europe in Welch (1997) illustrate some of the taxonomic difficulties that have been encountered with the species. Maus (1998) identified the distribution pattern of A. bipustulata, which includes all of Europe through North Africa to Pakistan and India. Therefore, the South Korean record of A. bipustulata in Cho and Ahn (2001) is highly doubtful. Park et al. (2011) recorded Aleochara verna for the first time from South Korea; therefore, the South Korean record of A. bipustulata might be a misidentification of A. verna. Further study in East Asia is needed to evaluate the true diversity of the subgenus Coprochara in the region. Zootaxa 3641 (3) © 2013 Magnolia Press · 219 TAXA/RUNNING TITLE 8 PT IN UPPER CASE FIGURES 44–45. Collecting localities of Aleochara (Coprochara) spp. based on specimens examined in Japan. 44. Aleochara (Coprochara) verna (Indicated by red circle) and A. (C.) binotata (Indicated by yellow square); 45. A. (C.) squalithorax (Indicated by blue triangle). Examined specimen data of Aleochara bipustulata. AUSTRIA: [Burgenland]: 1 ♂ , 1 ♀ , Illmitz, VI. 1995, K. Peschke leg. (without collecting date; det. Dr. C. Maus, 1996; KUM). Genital parts of both sexes were examined. This species is distinguished from A. verna and A. binotata by a much smaller coiled portion (1–5 coils) of the female spermatheca and the shape of a sclerite Z inside the median lobe of the aedeagus in the male (Maus, 1998). Diversity and distribution We recognized only three species as Japanese congeners of the subgenus Coprochara. This number is much smaller than the species counts in USA (seven species: Klimaszewski, 1984) and South Africa (six species: Klimaszewski & Jansen, 1994). However, it is very close to the number of the species in UK (four species: Welch, 1997) and South Korea (three species, although A. bipustulata is doubtful: Ahn et al., 2000; Cho & Ahn, 2001; Park et al., 2011). YAMAMOTO & MARUYAMA 220 · Zootaxa 3641 (3) © 2013 Magnolia Press Two species, A. verna and A. binotata, have wide global distribution ranges, but A. squalithorax is confined to East Asia. Aleochara verna is a Holarctic species and its presence in Japan is not surprising. In contrast, the finding of A. binotata from Japan is quite unexpected. This species has mainly been recorded from Europe. Previously, the easternmost record of this species was from east Siberia (Smetana, 2004). For that reason, the Japanese specimens represent the easternmost records of A. binotata. All of the Japanese specimens of this species were collected from Hokkaidô located in northeastern Japan, which has a continental climate (Fig. 44). Acknowledgements SY cordially thank associate professor Dr. Satoshi Kamitani in Kyushu University for continual guidance and support for the study in various ways. We express our sincere gratitude to Dr. Roger Booth (BMNH), Mr. Hirofumi Moriya (SCM) and Dr. Akiko Saitô (CBM) for loan of the institutional materials. Our thanks also due to the colleagues indicated in the material section for kindly providing us opportunities to examine the specimens. We thank Dr. Alfred F. Newton Jr. and Dr. Margaret K. Thayer in the Field Museum of Natural History, Chicago for kindly offering us literature references. Finally, we deeply indebted to anonymous reviewers for useful comments on the draft. 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ZooKeys, 121, 1–494. http://dx.doi.org/10.3897/zookeys.121.732 Welch, R.C. (1990) Aleochara binotata kr., not A. verna Say (Col.: Staphylinidae), a British insect. Entomologist’s Record, 102, 225–226. Welch, R.C. (1997) The British species of the genus Aleochara Gravenhorst (Staphylinidae). The Coleopterist, 6 (1), 1–45. Yamamoto, S. & Maruyama, M. (2009) Description of Aleochara (Maseochara) hiranoi sp.n. from Japan (Coleoptera: Staphylinidae: Aleocharinae). Koleopterogische Rundschau, 79, 65–70. Yamamoto, S. & Maruyama, M. (2012) Revision of the Seashore-dwelling Subgenera Emplenota Casey and Triochara Bernhauer (Coleoptera: Staphylinidae: genus Aleochara) from Japan. Zootaxa, 3517, 1–52. APPENDIX APPENDIX 1. Species list of Japanese names of Aleochara (subgenus Coprochara). Subgenus Coprochara Mulsant & Rey, 1874 Scientific name Japanese name Aleochara (Coprochara) verna Say, 1833 Futamon-higebuto-hanekakushi A. (C.) binotata Kraatz, 1856 Kibane-higebuto-hanekakushi A. (C.) squalithorax Sharp, 1888 Futo-tsuyakeshi-higebuto-hanekakushi