Acompocoris brevirostris Kerzhner, 1979

Yamada, Kazutaka & Yasunaga, Tomohide, 2021, The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics, Acta Entomologica Musei Nationalis Pragae 61 (2), pp. 375-426 : 384-386

publication ID

https://doi.org/ 10.37520/aemnp.2021.022

publication LSID

lsid:zoobank.org:pub:32519CC9-3658-469A-926D-6A1EBEE0FC59

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https://treatment.plazi.org/id/03D687AF-A136-FFFB-6AAE-F8F9FC508386

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Plazi

scientific name

Acompocoris brevirostris Kerzhner, 1979
status

 

Acompocoris brevirostris Kerzhner, 1979

( Figs 4A–D View Fig , 5A–C View Fig , 6A–D View Fig , 16A–B View Fig , 19 View Fig )

Acompocoris brevirostris Kerzhner, 1979: 23 . Holotype: J, Kuril Is., Urup, Kaymen (ZMAS).

Acompocoris brevirostris : KൾඋඓHඇൾඋ (1988): 773–774 (figures, in key); Pඣඋංർൺඋඍ (1996): 109 (catalogue, distribution); YൺඌඎඇൺGൺ et al.

(1999): 8 (record, distribution, photo); YൺඌඎඇൺGൺ (2001b): pl. 85, 280 (photo, diagnosis, habitat, prey, phenology); TඈGൺඌHං (2002): 8 (record, photo); Iංඃංආൺ (2004): 134 (record); KHඈආൾඇඍඈඏඌKඒ (2004): 182 (listed); KൺඇඒඎKඈඏൺ & MൺඋඎඌංK (2006): 164, 168 (listed); Gൺ- ඉඈඇ & Kඈඇඌඍൺඇඍංඇඈඏ (2008): 26 (listed); VංඇඈKඎඋඈඏ et al. (2010): 56 (catalogue, distribution); AඎKൾආൺ et al. (2013a): 84 (catalogue, distribution); VංඇඈKඎඋඈඏ & Gඈඅඎൻ (2016): 350–351 (listed, figure); Yൺආൺൽൺ et al. (2016): 422 (catalogue, distribution); VංඇඈKඎඋඈඏ (2020):39 (catalogue, distribution); VංඇඈKඎඋඈඏ & KHඋඎඅൾඏൺ (2021): 22 (distribution, habitat).

Material examined. JAPAN: HඈKKൺංൽඈ: 1 J ( Figs 4A–B View Fig ) 1 ♀

( Figs 4C–D View Fig ), Nakagawa-cho, Mt. Panke, 300–630 m, 31.vii.1997, T.

Yasunaga ( TKPM); 1 J ( Figs 6A–C View Fig ) 2 ♀♀ (one in Fig. 5A View Fig , one in

Fig. 6D View Fig ), same locality and date, S. Yamashita ( TKPM); 1 J 2 ♀♀,

Kamikawa-cho, Mts. Taisetsu, Mt. Midori-dake, 1500–1700 m alt.,

43.640N 142.923E, Pinus pumila , 7.viii.2001, T. Yasunaga ( TYCN); 1

♀, Kamikawa-cho, Goshikigahara, 12.viii.1998, A.Yamamoto ( TKPM);

1 J, Mt.Antaroma-dake, 11.viii.1967, A. Nakanishi ( ELKU); 1 J, Mt.

Satsunai-dake, 28.vii.1967,A. Nakanishi ( ELKU). HඈඇඌHඎ: Yamagata

Pref.: 2 ♀♀, Mt. Chôkai, 17.ix.1971, M. Tomokuni ( NSMT). Gunma

Pref.: 1 ♀, Katashina-mura, Tokura, 17.x.2014, K. Takahashi ( TKPM).

Nagano Pref.: 1 ♀, South Alps, Mt. Senjôga-take, 2.x.2011, S. Shiyake

( OMNH); 3 JJ (one in Figs 5B–C View Fig ) 14 ♀♀, Ôtaki-mura, Tanohama,

7. viii.2010, T. Ban ( TKPM). Gifu Pref.: 1 J 1 ♀, Mt. Norikura-dake,

7.ix.1951, H. Hasegawa ( OMNH).

Differential diagnosis. Recognized by the following combination of characters: body ( Figs 4A–D View Fig , 16A–B View Fig ) generally blackish brown; antennal segment II approximately 1.2 times as long as head width across eyes; labium ( Figs 4B,D View Fig ) reaching near middle of mesosternum; hemelytra ( Figs 4A,C View Fig ) tinged with reddish brown, female ( Fig. 4C View Fig ) much paler with dark spot near middle of endocorium; membrane of hemelytra smoky dark brown, with area behind apex of cuneus and area along four veins grayish white; apex of femora and entire tibiae reddish brown to yellowish brown. Similar to Holarctic A. pygmaeus (Fallén, 1807) and Palaearctic A. alpinus Reuter, 1875 , but distinguished from both by labium reaching near middle of mesosternum (in A. pygmaeus and A. alpinus , labium extending or almost reaching metacoxae) and paramere basally widened (in A. pygmaeus and A. alpinus , narrower). The form of female genitalia of A. brevirostris is similar to that of A. alpinus with a copulatory tube possessing a lateral process at base but separated from that species by the copulatory tube being fused on the left side of the intersegmental membrane between sterna VII and VIII in dorsal view (in A. alpinus , fused on the mesal part of the intersegmental membrane) and the copulatory tube being rather short (in A. alpinus , much longer).

Redescription. Male genitalia ( Figs 5B–C View Fig , 6A–C View Fig ): Pygophore ( Fig. 6A View Fig ) broadly cone-shaped, covered with 4–5 long, stout setae (missing in Fig. 6A View Fig ) intermixed with short, suberect setae along outer margin and on posteroventral surface, of which the longest setae are approximately half the length of pygophore; mid-dorsal surface very hirsute with short, suberect setae; paramere ( Figs 5C View Fig , 6B–C View Fig ) lamellate, short, strongly curved near apex, basally widened, with a few very short, erect setae on middle portion, without distinct groove but weak depression near base formed by inflection of posterior edge.

Female genitalia ( Fig. 6D View Fig ): Copulatory tube fused on left lower surface of intersegmental membrane between sterna VII and VIII in dorsal view, approximately 0.3 mm in length, with lateral process at base, somewhat narrowing toward apex, entire copulatory tube with rugosities; thin-walled, annular structures of unknown function visible within sperm pouch at junction of pouch and copulatory tube; trunk of conductive tissue not pronounced (or possibly dissolved).

Measurements [mm; JJ (n = 5) / ♀♀ (n = 10)]. Body length 3.85–4.00 / 4.10–4.50; head length (excl. neck) 0.46–0.50 / 0.45–0.51; head width across eyes 0.51–0.56 / 0.53–0.58; vertex width 0.29–0.33 / 0.31–0.34; length of antennal segments I – 0.20–0.23 / 0.20–0.23, II – 0.63–0.69 / 0.60–0.65, III – 0.36–0.39 / 0.36–0.41, and IV – 0.35–0.40 / 0.35–0.43; length of labial segments II – 0.20–0.23 / 0.21–0.26, III – 0.69–0.75 / 0.65–0.80, and IV – 0.29–0.31 / 0.30–0.35; anterior pronotal width 0.43–0.45 / 0.44–0.50; mesal pronotal length 0.48–0.53 / 0.50–0.55; basal pronotal width 1.18–1.25 / 1.28–1.44; length of embolial margin 1.22–1.31 / 1.22–1.48; length of cuneal margin 0.90–0.95 / 1.00–1.15; maximum width across hemelytra 1.46–1.55 / 1.63–1.85.

Bionomics. Acompocoris brevirostris is associated with Pinus pumila (Pall.) Regel (e.g., KൾඋඓHඇൾඋ 1979, 1988; YൺඌඎඇൺGൺ 2001b; TඈGൺඌHං 2002; KHඈආൾඇඍඈඏඌKඒ 2004). In the treeless areas of the Chukotka Autonomous Okrug (tundra zone and the elfin wood subzone) in Far East Russia, it was collected on a swamp river terrace with sedge-sphagnum-moss cover and shrubs of dwarf pine and alder (VංඇඈKඎඋඈඏ & KHඋඎඅൾඏൺ 2021).

Distribution. Japan: Hokkaido (YൺඌඎඇൺGൺ et al. 1999); Honshu: Yamagata *, Gunma *, Ishikawa (TඈGൺඌHං 2002), Nagano *, Gifu *. Chishima (Kuril) Islands: Kunashir Is., Iturup Is., Urup Is., Simushir Is., Ketoi Is., Shiashkotan Is., Paramushir Is., Shumshu Is. (KൾඋඓHඇൾඋ 1979, Kൺ- ඇඒඎKඈඏൺ & MൺඋඎඌංK 2006). Russia: Far East: Magadan, Kamchatka, Sakhalin, Primorsky Kray (KൾඋඓHඇൾඋ 1988, VංඇඈKඎඋඈඏ et al. 2010, VංඇඈKඎඋඈඏ & Gඈඅඎൻ 2016). In Japan, this species is apparently restricted to the subalpine coniferous forests of the central and northern parts of the country, generally at high elevations but also in the lowland areas of Hokkaido where Pinus pumila subalpine forests can be found.

TKPM

Tokushima Prefectural Museum

NSMT

National Science Museum (Natural History)

OMNH

Osaka Museum of Natural History

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Hemiptera

Family

Anthocoridae

Genus

Acompocoris

Loc

Acompocoris brevirostris Kerzhner, 1979

Yamada, Kazutaka & Yasunaga, Tomohide 2021
2021
Loc

Acompocoris brevirostris

KERZHNER I. M. 1979: 23
1979
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