Aleochara (Emplenota) hayamai Yamamoto & Maruyama
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.6175374 |
persistent identifier |
https://treatment.plazi.org/id/78D98C08-C254-4C5C-A2DB-E5B119C07D13 |
taxon LSID |
lsid:zoobank.org:act:78D98C08-C254-4C5C-A2DB-E5B119C07D13 |
treatment provided by |
Plazi |
scientific name |
Aleochara (Emplenota) hayamai Yamamoto & Maruyama |
status |
sp. nov. |
Aleochara (Emplenota) hayamai Yamamoto & Maruyama View in CoL n. sp.
( Figs. 3 View FIGURES 1 – 7 , 38–45 View FIGURES 38 – 45 , 93–94, 97 View FIGURES 93 – 100 , 103 View FIGURES 101 – 103 )
Type series. Holotype, 3, JAPAN: Koura-kaigan, Koura, Kashima-chô, Matue-shi, Shimane-ken, Honshû (35.521N, 132.975E), 18 VII 2010, Yamamoto-S. (by hand with aspirator; under flotsam on sandy beach in the hot daytime; KUM).
Paratypes, JAPAN: [Honshû]: 2 3, Mito beach, Hasse-machi, Miura-shi, Kanagawa-ken (35.177N, 139.620E), 14 V 2009, Watanabe-T. (cWat); 1 3, Inugu (Dôgo Is., Oki-shotô), Okinoshima-chô, Oki-gun, Shimane-ken (36.219N, 133.372E *), 10 XI 2009, Hayama-T. (cHayam); 4 3, 3 Ƥ, Kakanokuketo, Shimane-chô, Matsue-shi, Shimane-ken (35.578N, 133.051E), 1 IV 2009, Hayama-T. (shingle beach; cHayam); 2 3, 2 Ƥ, same data, but 9 VI 2009; 2 3, same data, but 18 VII 2010, Yamamoto-S. (cYam); 1 3, same data, but 19 VII 2010; 1 3, Kaka (Katsura-jima), Shimane-chô, Matsue-shi, Shimane-ken (35.566N, 133.052E), 19 VII 2010, Yamamoto-S.
(by hand pick; sandy beach; under seaweed around evening; cYam); 18 3, 4 Ƥ, Koura-kaigan, Koura, Kashimachô, Matue-shi, Shimane-ken (35.521N, 132.975E), 8-10 VI 2009, Hayama-T. (FIT; cHayam); 31 3, 26 Ƥ, same data, but 18-20 VI 2009; 3 3, same data, but 3-5 VII 2009; 4 3, 8 Ƥ, same data, but 16-18 VII 2009; 8 3, 4 Ƥ, same data, but 17 VII 2010, Yamamoto-S. (by hand pick up with aspirator; under flotsam on sandy beach; KUM); 1 3, 2 Ƥ, same data, but 18 VII 2010 (same data as holotype); 2 3, Sakaura-kaigan, Sakaura-chô, Izumo-shi, Shimane-ken (35.508N, 132.861E), 20 IV 2009, Hayama-T. (cHayam); 1 Ƥ, same data, but 15 V 2009; 1 Ƥ, river mouth of Sakaura-gawa, Sakaura-chô, Izumo-shi, Shimane-ken (35.508N, 132.861E), 13 IV 2008, Hayama-T. (cHayam); 1 3, same data, but 31 IV 2008; 1 3, same data, but 17 V 2008; 1 3, 31 VIII 2008; 1 3, same data, but 5 VIII 2009; 2 3, 1 Ƥ, Owashi-hama, Nakayama, Taisha-chô, Izumo-shi, Shimane-ken (35.433N, 132.634E), 24 III 2009, Hayama-T. (shingle beach; cHayam); 1 3, 1 Ƥ, Akaishihana, Hinomisaki, Taisha-chô, Izumo-shi, Shimane-ken (35.411N, 132.650E *), 2 IV 2009, Hayama-T. (cHayam); 7 Ƥ, same data, but 2-8 V 2009 (FIT); 1 3, Kiami-chô, Masuda-shi, Shimane-ken (34.676N, 131.747E), 10-11 V 2009, Hayama-T. (FIT; cHayam). [Kyûshû]: 1 3, Odo-kôen park, Odo-2chôme 6, Nishi-ku, Fukuoka-shi, Fukuoka-ken (33.596N, 130.311E), 28 VI 2009, Yamamoto-S. (from seaweed on sandy beach with Aleochara (E.) segregata ; cYam); 2 3, Sato (Kamikoshikijima), Sato-machi, Satsumasendai-shi, Kagoshima-ken (31.844N, 129.919E), 11-12 IV 1973, Furuki-Y. ( EEEU).
Description. Body ( Fig. 3 View FIGURES 1 – 7 ): small to medium sized, slender body; surface of pronotum and elytra somewhat densely haired by rather short and thin setae; fore-body (head, pronotum and elytra) weakly shining due to extremely minute hexagonal microstructures. Colour ( Fig. 3 View FIGURES 1 – 7 ): gland colour complete black; legs dark brown to reddish brown, tarsal segments orange brown to reddish brown: maxillary and labial palpi blackish brown to yellowish brown; antennae blackish brown and partly reddish brown. Head: impunctured area along midline not uniquely elevated at all. Antennae ( Fig. 42 View FIGURES 38 – 45 ): entirely slender; slightly longer than combined length of head and pronotum; segment I, nearly 2.8 times as long as broad; segment II somewhat shorter than I; segment III as same length as II; segments IV and V long barrel shape, clearly longer than width; segments VI to VII short barrel shape; segments VIII to X transverse; last segment somewhat long, about 1.7 times as long as broad; relative length (width) of segments from basal to apical: 11(4): 7(3): 6.5(3): 4(3): 4.5(3.5): 4(4): 4(4): 5(5): 6(5): 4.5(5): 10(6). Thorax: pronotum somewhat strongly convex above, with moderately rounded posterior margin; slightly wider than long (PW/PL =1.23), clearly broader than head (PW/HW =1.38), widest just behind middle; surface with extremely minute hexagonal reticulations with inconspicuous punctures. Metaventrite, about 1.6 times as long as mesoventrite. Inter coxal process of mesoventrite sharply pointed with very short carina along midline, about 0.3 times as long as mesoventrite. Inter coxal process of metaventrite broad and somewhat long, and apical margin pointed moderately. Legs: relative lengths of tarsomeres from basal to apical: 4.5: 3: 3: 3: 10 in foretarsus, 6: 5: 5: 5: 13 in midtarsus, 8: 6: 6: 6: 16 in hindtarsus.
[Male]: posterior margin of tergite VIII ( Fig. 38 View FIGURES 38 – 45 ) very weakly emarginated medially, with around 7 to 8 macrosetae. Sternite VIII ( Fig. 40 View FIGURES 38 – 45 ) with about 12 macrosetae; posterior margin very strongly pointed toward apex, forming triangular. Median lobe of aedeagus ( Figs. 43–44 View FIGURES 38 – 45 ) C-curved (sponge-gourd shape) in lateral view ( Fig. 43 View FIGURES 38 – 45 ); moderately narrowed apically in ventral view ( Fig. 44 View FIGURES 38 – 45 ); a pair of subapico-ventral projections thick, robust and straight in lateral view ( Fig. 43 View FIGURES 38 – 45 ); basal swelling of aedeagus, circularly rounded in lateral view ( Fig. 43 View FIGURES 38 – 45 ); apical lobe of median lobe very short isosceles shape in ventral aspect ( Fig. 44 View FIGURES 38 – 45 ); flagellum extremely longer than the whole length of median lobe ( Figs. 43–44 View FIGURES 38 – 45 ).
[Female]: posterior margin of tergite VIII ( Fig. 39 View FIGURES 38 – 45 ) slightly rounded, but very weakly emarginated medially, with about 7 macrosetae. Posterior margin of sternite VIII ( Fig. 41 View FIGURES 38 – 45 ) rounded or weakly pointed, with around 8 macrosetae. Spermatheca ( Fig. 45 View FIGURES 38 – 45 ): spermathecal head as long as apical portion of spermathecal stem; basal portion of spermathecal stem very short and curved; sclerotized portion of spermathecal stem thin and erect; each part of spermatheca except for membraneous portion of spermathecal duct (sm) entirely and very weakly sclerotized; (sm) extremely long in length.
Measurements (male: n=10): BL, 2.94–4.65 (4.00±0.49); FBL, 1.66–2.07 (1.87±0.15); HL, 0.46–0.68 (0.56±0.07); HW, 0.53–0.69 (0.60±0.05); AL, 1.11–1.51 (1.30±0.14); PL, 0.59–0.78 (0.69±0.06); PW, 0.60–0.92 (0.83±0.06); EL, 0.57–0.77 (0.67±0.06); EW, 0.94–1.27 (1.08±0.10); HTL, 0.57–0.79 (0.66±0.07).
Measurements (female: n=10): BL, 3.23–4.64 (4.04±0.38); FBL, 1.50–2.11 (1.91±0.20); HL, 0.44–0.62 (0.55±0.05); HW, 0.51–0.66 (0.60±0.04); AL, 1.03–1.32 (1.18±0.09); PL, 0.53–0.73 (0.66±0.07); PW, 0.68–0.91 (0.83±0.07); EL, 0.62–0.77 (0.69±0.05); EW, 0.87–1.18 (1.07±0.10); HTL, 0.55–0.78 (0.68±0.07).
Distribution. [ JAPAN]: Honshû, Kyûshû, Dôgo Is., Kamikoshiki-jima. See, Fig. 103 View FIGURES 101 – 103 .
Diagnosis. Aleochara hayamai is a peculiar species and can be easily discriminated from other Japanese Emplenota species by following character states: small to medium size body (not large species); gland colour completely black and somewhat strongly shining even in mat area of the forebody (hexagonal structures on dorsal surface very minute compared to the other Japanese Emplenota species), and deep punctures of dorsal surface on forebody inconspicuous ( Fig. 3 View FIGURES 1 – 7 ); longitudinal impunctured area of head along midline not uniquely elevated at all; lateral margin of pronotum somewhat convex toward anterolaterally; antennae entirely slender, especially segments IV to V which close to long barrel shape rather than spherically short barrel shape ( Fig. 42 View FIGURES 38 – 45 ); legs somewhat long and slender (HTL =0.67). [Male]: sternite VIII ( Fig. 40 View FIGURES 38 – 45 ) sharply pointed toward posterior, making sharp triangular; median lobe of aedeagus ( Figs. 43–44 View FIGURES 38 – 45 ) unique with extremely long flagellum; subapico-ventral projections of median lobe robust and straight in lateral view ( Fig. 43 View FIGURES 38 – 45 ). [Female]: spermatheca ( Fig. 45 View FIGURES 38 – 45 ) unique in shape; very weakly sclerotized uniformely, with short basal portion of spermathecal stem and extraordinary long membraneous portion of spermathecal duct.
Etymology. The species, Aleochara hayamai , is dedicated to Mr. Takeshi Hayama (Okinawa-ken), who found this species for the first time during his ecological survey of coastal insects in Shimane-ken.
Remarks. Numerous individuals were collected by Mr. T. Hayama in Shimane-ken (Honshû). He researched the entire coastal region of Shimane-ken to study coastal insect ecology and succeeded in collecting a few specimens of A. hayamai . Mr. Hayama discovered its peculiarity and sent us the specimen. We examined more than 2,000 specimens of Emplenota from all over Japan, but this species seems to be rare except in Shimane-ken and we found it from only three other localities. Aleochara hayamai has similar external characters to other Japanese species, however, the species is outstanding by having huge and peculiar male genitalia.
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.
Kingdom |
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Phylum |
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Class |
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Order |
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Family |
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Tribe |
Aleocharini |
SubTribe |
Aleocharina |
Genus |
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SubGenus |
Emplenota |