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Research Article
A revision of the genus Trichohoplorana Breuning, 1961 (Arthropoda, Insecta, Coleoptera, Cerambycidae, Lamiinae, Acanthocinini)
expand article infoGui-Qiang Huang, Dong-Shuo Liu§, Rong-Chuan Xiong
‡ Liupanshui Normal University, Liupanshui, China
§ Unaffiliated, Beijing, China
Open Access

Abstract

A taxonomic revision of the genus Trichohoplorana Breuning, 1961 is presented. A junior synonym of Trichohoplorana, Ipochiromima Sama & Sudre, 2009, syn. nov., is proposed. A junior synonym of T. dureli Breuning, 1961, I. sikkimensis (Breuning, 1982), syn. nov., is proposed. Trichohoplorana is newly recorded from Vietnam. A new species, T. nigeralba sp. nov. is described from Vietnam. Trichohoplorana luteomaculata Gouverneur, 2016 is newly recorded from China and Vietnam. Hind wings and male terminalia of T. luteomaculata are described for the first time. Trichohoplorana is redescribed, and a key to Trichohoplorana species is presented.

Keywords

Hind wings, male terminalia, new faunistic records, new species, synonyms

Introduction

The genus Trichohoplorana was established by Breuning (1961) for Trichohoplorana dureli Breuning, 1961. It presently consists of six species from Asia (Tavakilian and Chevillotte 2022). Mitono (1943) described Acanthocinus shirakii from China (Taiwan), then Gressitt (1951) transferred A. shirakii Mitono, 1943 to Neacanista Gressitt, 1940, and finally, Gouverneur (2016) transferred N. shirakii to Trichohoplorana and described T. luteomaculata from Laos (Houa Phan). Holzschuh (1989, 1990, 2015) described T. juglandis, T. mutica, and T. tenuipes, respectively, from South Asia.

In this work, new synonyms, new faunistic records, and a new species are provided. Wings and male terminalia are described for the first time. Consequently, Trichohoplorana now consists of seven species from Asia. A redescription and a key to all species of Trichohoplorana are presented.

Material and methods

Specimens examined are deposited in following institutions and private collections:

CDSL Collection Dong-Shuo Liu, Beijing, China

CHS Collection Carolus Holzschuh, Villach, Austria

CWW Collection Andreas Weigel, Wernburg, Germany

CXG Collection Xavier Gouverneur, Rennes, France

LPSNU School of Biological Science and Technology, Liupanshui Normal University, Liupanshui, Guizhou, China

MNHN Muséum national d’Histoire naturelle, Paris, France

SYSU The Museum of Biology, Sun Yat-sen University, Guangzhou, China

The methods of taking photographs for Figs 2C–G, 4B–F, 6A–E followed Huang et al. (2020), and methods of photographing Fig. 3A–J mainly followed Huang and Li (2019) but were taken with a E3ISPM21000KPA camera and ImageView software. The terminology of hind wings vein follows Švácha and Lawrence (2014). The terminology of male terminalia follows Ślipiński and Escalona (2013).

Taxonomy

Trichohoplorana Breuning, 1961

Trichohoplorana Breuning, 1961: 548; Breuning 1963: 534; Breuning 1978: 49; Löbl and Smetana 2010: 213. Type species: Trichohoplorana dureli Breuning, 1961, by original designation.

Trichhoplorana Breuning 1977: 115 (misspelling).

Ipochiromima Sama and Sudre 2009: 384 (replacement name for Mimipochira Breuning, 1982: 25); Löbl and Smetana 2010: 209. Type species: Mimipochira sikkimensis Breuning, 1982, by original designation. Syn. nov.

Redescription

Head distinctly narrower than prothorax, frons with a narrow, median furrow extending from base of clypeus up to apical margin of pronotum; eyes coarsely faceted, lower lobes of eyes distinctly far away from each other and longer than genae; antennae slender, distinctly longer than body, scape strongly expanded before apex, pedicle distinctly longer than broad. Pronotum transverse, with a tubercle on each side, punctured, with a pair of subuliform tubercles at sides of middle; prosternal process broad, with a longitudinal depression in middle, procoxal cavities closed posteriorly. Scutellum linguiform. Elytra covered with black or brown spots and a series of black or brown spots along suture; disc elongate, distinctly broader than pronotum at base, gradually narrow from near apical third, punctured, with a pair of tubercles at base and near scutellum, with a pair of bumps behind the tubercles; humeral angles rounded and slightly processed forward. Mesocoxal cavities closed externally to mesepimera. Femora strongly clavate.

Diagnosis

Trichohoplorana is very similar to Neacanista Gressitt, 1940 in having the pronotum with a tubercle at each side, with a pair of tubercles at the sides of the middle, the elytra with a pair of tubercles at the base and near the scutellum, with a pair of bumps behind the tubercles, and a strongly clavate femora. However, Trichohoplorana differs from Neacanista in having the antennal scape strongly expanded before the apex (gradually thickened before the apex in Neacanista) and the pedicle distinctly longer than broad (broader than long in Neacanista).

Distribution

Bhutan, China, India, Laos, Nepal, Vietnam (new country record).

Remarks

Breuning (1982) established Mimipochira for M. sikkimensis Breuning, 1982, but this genus was a junior homonym of Mimipochira Breuning, 1956. Hence, Sama and Sudre (2009) introduced the new name Ipochiromima. After comparing photographs of the holotypes of T. dureli Breuning, 1961 (Fig. 1A) and M. sikkimensis (Fig. 1B, C), we consider these two species as belonging to the same genus, based on above redescribed characters. Thus, we treat Ipochiromima as a junior synonym of Trichohoplorana.

Figure 1. 

Types of Trichohoplorana spp. A Trichohoplorana dureli, holotype, male habitus, dorsal view (photo by Andreas Weigel) B–D Mimipochira sikkimensis B holotype, male habitus, dorsal view C holotype, male habitus, lateral view D labels (photos by Xavier Gouverneur) E Trichohoplorana juglandis, holotype, male habitus, dorsal view (photo reproduced from Holzschuh 1989) F Trichohoplorana mutica, holotype, male habitus, dorsal view (photo reproduced from Holzschuh 1990) G, H Trichohoplorana tenuipes G holotype, male habitus, dorsal view H paratype, female habitus, dorsal view (photos provided by Holzschuh) I, J Acanthocinus shirakii: I holotype, male habitus, dorsal view J labels (photos reproduced from Huang et al. 2015).

Trichohoplorana dureli Breuning, 1961

Fig. 1A–D

Trichohoplorana dureli Breuning, 1961: 548 (type locality: “Pedong, Sikkim, India”); Breuning 1963: 534 (catalogue); Breuning 1978: 49 (redescription), pl. IV, fig. 15 (holotype); Löbl and Smetana 2010: 213 (catalogue).

Ostedes dureli: Breuning and Heyrovský 1961: 143.

Mimipochira sikkimensis Breuning, 1982: 26 (type locality: “Sikkim, India”). Syn. nov.

Ipochiromima sikkimensis: Sama and Sudre 2009: 384 (catalogue); Löbl and Smetana 2010: 209 (catalogue).

Type material examined

Trichohoplorana dureli Breuning, 1961: holotype, ♂ (MNHN), Pedong, Sikkim, India, 1914, L. Durel leg., [examined from a photograph (Fig. 1A)]; Mimipochira sikkimensis Breuning, 1982: holotype, ♂ (MNHN), Sikkim, India [examined from three photographs (Fig. 1B–D)].

Distribution

Bhutan, India (Sikkim).

Remarks

The differences between T. dureli and I. sikkimensis (Fig. 1A–C) mainly reflect in the shape of the elytral brown spots: the large spots near elytral middle, at apical third, and at apex. They are actually intraspecific differences; thus, we treat I. sikkimensis as a junior synonym of T. dureli.

Trichohoplorana juglandis Holzschuh, 1989

Fig. 1E

Trichohoplorana juglandis Holzschuh, 1989: 401 (type locality: “Menchunang, East Dochu-La, Thimphu district, West Bhutan”), fig. 8 (holotype, male); Löbl and Smetana 2010: 213 (catalogue); Weigel 2012: 408 (catalogue), pl. XXVII, fig. b; Lazarev 2019: 154 (catalogue).

Distribution

Bhutan (Thimphu), India (Arunachal Pradesh).

Trichohoplorana mutica Holzschuh, 1990

Fig. 1F

Trichohoplorana mutica Holzschuh, 1990: 193 (type locality: “Footpath from Sherpagaon to Ghora Tabela, Langtang Khola, Nawakot, C-Nepal”), fig. 11 (holotype, male); Weigel 2006: 506 (catalogue); Löbl and Smetana 2010: 213 (catalogue).

Distribution

Nepal (Nawakot).

Trichohoplorana tenuipes Holzschuh, 2015

Fig. 1G, H

Trichohoplorana tenuipes Holzschuh, 2015: 473 (type locality: “Bhalukhop, district of Taplejung, East Nepal”), figs 3 (holotype, male) and 4 (paratype, female).

Type material examined

Holotype , ♂ (CHS), Bhalukhop, district of Taplejung, East Nepal, alt. 3000m, 11–21.V.2013, Emil Kučera leg., [examined from a photograph (Fig. 1G)]; paratype, 1 ♀ (CHS), data same as holotype, [examined from a photograph (Fig. 1H)].

Distribution

Nepal (Taplejung).

Trichohoplorana shirakii (Mitono, 1943)

Fig. 1I, J

Acanthocinus shirakii Mitono, 1943: 584 (type locality: “Reimei, Hassenzan, Taiwan”).

Neacanista shirakii: Gressitt 1951: 518 (catalogue); Breuning 1978: 40 (redescription); Hua 1982: 99 (catalogue); Nakamura, Makihara and Saito 1992: 95 (catalogue); Hua 2002: 218 (catalogue); Chou 2004: 326, fig (male); Hua et al. 2009: 95, pl. XCV, fig. 1091 (male and female); Löbl and Smetana 2010: 210 (catalogue); Huang et al. 2015: 560 (catalogue), figs 32 (holotype, male), 33 (holotype, labels), and 34 (4 in map).

Trichohoplorana shirakii: Gouverneur 2016: 72, figs 2a (holotype, male) and 2b (holotype, labels).

Distribution

China (Taiwan).

Trichohoplorana luteomaculata Gouverneur, 2016

Figs 2, 3, 4, 5

Trichohoplorana luteomaculata Gouverneur, 2016: 69 (type locality: “Ban Saleui, Massif du Mont Phou Pan, Houa Phan Province, Northeast Laos”), figs 1a, b (holotype, male) and 1c (paratype, female).

Type material examined

Holotype , ♂ (CXG), Ban Saleui, Massif du Mont Phou Pan, Houa Phan Province, Northeast Laos, alt. 1300–1900m, 1.V.2012, local collector leg., [examined from two photographs (Fig. 2A, B)]; paratype, 1 ♀ (CXG), data same as holotype, but 2.V.2014 [examined from a photograph (Fig. 4A)].

Figure 2. 

Trichohoplorana luteomaculata, males A, B holotype habitus A dorsal view B lateral view (photos by Xavier Gouverneur) C–G material from Hainan, China C habitus, dorsal view D habitus, lateral view E habitus, ventral view F head, frontal view G right hind wing, dorsal view. Abbreviations: A: anal, Cu: cubital, MP: medial posterior, MS: medial spur, ?: a vein of uncertain homology (either a crossvein or base of MP3+4 vein). Scale bars: 5 mm (a); 1 mm (b).

Figure 3. 

Male terminalia of Trichohoplorana luteomaculata from Hainan, China A tergite VIII, dorsal view B sternite VIII, verntral view C spiculum gastrale, dorsal view D–F tegmen D dorsal view E ventral view F lateral view G–J penis G dorsal view H dorsal view I ventral view J lateral view. Not to scale.

Figure 4. 

Trichohoplorana luteomaculata, females A paratype habitus, dorsal view (photo by Xavier Gouverneur) B–F material from Hainan, China B habitus, dorsal view C habitus, lateral view D habitus, ventral view E head, frontal view F right hind wing, dorsal view. Abbreviations: A: anal, Cu: cubital, MP: medial posterior, MS: medial spur, ?: a vein of uncertain homology (either a crossvein or base of MP3+4 vein). Scale bars: 5 mm (a), 1 mm (b).

Additional material examined

China: 1 ♀ (SYSU), Suoli village, Tongdao County, Huaihua City, Hunan Province, V.1981, Li-Jun Zhang leg.; 1♂1♀ (CDSL, figs 2C–G, 3, 4B–F), Jianfengling National Natural Reserve, Hainan Province, 7.VI.2021, 18°42'34.75"N, 108°52'34.50"E, alt. 954 m, Dong-Shuo Liu leg., collected by light trap (Fig. 5); Vietnam: 1 ♀ (LPSNU), Yen Bai Province, August 2020, local collector leg.; 1 ♀ (CWW), Gem. Ta Pin, Kreis Sapa, Lao Cai Province,22°22.196'N, 103°48.701'E, alt. 2318 m, 26.VI–01.VII.2017, N.H. Binh leg., [examined from a photograph provided by Andreas Weigel].

Figure 5. 

Scene showing collecting Trichohoplorana luteomaculata by light trap from Hainan, China (photos by Dong-Shuo Liu).

Supplementary description

Male (Figs 2C–G, 3). Hind wings (Fig. 2G) with AA3+4 vein bifurcate near apical third; AA4 vein and AA3 vein closed to each other apically and not extending to margin; AA3 vein connected with Cu vein near apical third; CuA2 vein connected with MP3+4 vein near basal third of MP3+4 vein and not extending to margin; MP3+4 vein bifurcate near middle; MP4 vein, MP3 vein and MS vein not extending to margin; a short and vague uncertain vein (?, either a crossvein or base of MP3+4 vein) located between Cu vein and MP1+2 vein.

Male terminalia. Tergite VIII (Fig. 3A) sparsely covered with short brown setae apically and at sides of apical third, nearly truncated at apex. Sternite VIII (Fig. 3B) anchor-shaped, sparsely covered with short brown setae at apical sides, apical margin slightly depressed; spiculum relictum distinctly longer than sternite VIII. Stem of spiculum gastrale more than 2.0 times as long as branches and curved towards dorsum at base (Fig. 3C). Parameres of tegmen sparsely covered with short brown setae on apical third and several long setae near apical fifth; each paramere gradually constricted from base to apex, but external margin slightly expanded near apex; apex of both parameres rounded and closed together; phallobase nearly 3.0 times as long as parameres and processed outward near middle; anterior tegminal strut curved outward (Fig. 3D–F). Penis curved towards venter, ventral plate distinctly longer and broader than dorsal plate and slightly sharp at apex; dorsal plate widely rounded at apex; apex of dorsal struts obliquely truncated (Fig. 3G–J).

Female (Fig. 4B–F). Hind wings (Fig. 4F) with AA3+4 vein bifurcate near apical third; AA4 vein and AA3 vein fused apically and not extending to margin; AA3 vein connected with Cu vein near apical third; CuA2 vein connected with MP3+4 vein near basal fifth of MP3+4 vein and not extending to margin; MP3+4 vein bifurcate near middle, MP4 vein, MP3 vein and MS vein not extending to margin; a short uncertain vein (?, either a crossvein or base of MP3+4 vein) located between Cu vein and MP1+2 vein.

Distribution

China (Hainan, Hunan), Laos (Houa Phan), Vietnam (Lao Cai, Yen Bai).

Trichohoplorana nigeralba sp. nov.

Fig. 6

Type material examined

Holotype , ♀ (LPSNU), Yen Bai Province, Vietnam, V.2019, local collector leg.

Description

Female, holotype. Body length: 14.0 mm, humeral width: 5.2 mm. Body black, antennal scape (except for outside of apex), pedicel, antennomeres III (except for apex), IV (except for apex), V (basal half), VI (basal half), elytra (apical half), protibiae (basal half), mesofemora (basal half), mesotibiae (basal half), metafemora (most of parts) and metatibiae (basal half) reddish brown; claws yellowish brown (Fig. 6A–C).

Figure 6. 

Trichohoplorana nigeralba, holotype, female A habitus, dorsal view B habitus, lateral view C habitus, ventral view D head, frontal view E right hind wing, dorsal view. Abbreviations: A: anal, Cu: cubital, MP: medial posterior, MS: medial spur, ?1: a vein of uncertain homology (either a crossvein or base of MP3+4 vein), ?2: an uncertain vein. Scale bars: 5 mm (a), 2 mm (b).

Frons (Fig. 6D) densely covered with short yellow and white hairs. Vertex densely covered with short white hairs on middle and short yellow hairs on center (Fig. 6A). Antennae sparsely covered with sub-erect, short, white setae; scape sparsely covered with short, brown setae; pedicel sparsely covered with short, brown setae, with several short, white setae at internal side of apex; antennomere III sparsely covered with short, white setae basally, other parts densely with short, brown setae; antennomeres IV–XI densely covered with short white setae on the basal half and densely with short, brown setae on the apical half; antennomeres III–VII fringed with several long, black setae ventrally; antennomeres VIII–X fringed with one or two long, black setae ventrally; antennae 1.5 times as long as body, length (mm) of each antennomere: scape = 2.7, pedicel= 0.8, III = 3.0, IV= 3.0, V = 2.2, VI = 2.0, VII = 1.7, VIII = 1.6, IX = 1.6, X = 1.5, X I = 1.3; antennomeres III and IV curved inward (Fig. 6A–C). Pronotum (Fig. 6A) covered with three yellow haired bands: two located at sides and starting from near anterior margin to posterior margin, one located in middle and starting from anterior margin to posterior margin; disc with a pair of subtriangular, yellow haired spots located at sides of middle; near anterior of pronotum distinctly expanded outward, pronotum densely punctured (except for apex and base), base of the subuliform tubercles on pronotum expanded forward. Prosternum (sides) and propleuron (venter) sparsely covered with short, yellow hairs (Fig. 6B, C). Scutellum (Fig. 6A) sparsely covered with short black hairs, densely covered with yellow hairs at apex, depressed in middle of apical margin. Elytra (Fig. 6A, B) sparsely covered with short black hairs on the basal half, a short yellow haired band at lateral margins of base, several yellow haired spots arranging into an longitudinal line starting from near posterior humeral angle to basal third, a yellow haired spot located behind the bumps, and several yellow spots along suture from basal fourth to middle; the tubercles at elytral base and near scutellum, and the bumps behind the tubercles densely covered with short, black setae; apical half of each elytron densely covered with short white hairs and four longitudinal yellow haired bands (first band located at lateral margin, second and third bands located in middle and fused at apical half, forth band located near suture); disc 1.9 times as long as wide at base, rounded apically, moderately covered with dense coarse punctures at basal half. Mesosternum, mesepisternum, and mesepimeron sparsely covered with short, yellow hairs; metasternum, metepisternum, and metepimeron densely covered with short, yellow hairs (Fig. 6C). Femora sparsely covered with short white setae and several suberect, long, white setae at external side; tibiae covered with extremely sparse, suberect, long, white setae, sparsely with short, thin, black setae on the basal third, densely with short, white setae in middle, and densely with short, thick, black setae on the apical third; tarsomere I–III (except for venter) densely covered with short white and sparsely suberect, long, white setae dorsally, tarsomere V (except for venter) sparsely covered with short, white setae at basal half and short, black setae on the apical half, with more sparse long black setae at apex (Fig. 6A–C). Abdominal ventrites I–V densely covered with short, yellow hairs, the hairs more dense at apices of ventrites I–IV; apex and sides of ventrite V sparsely covered with long, yellow pubescences (Fig. 6C).

Hind wings (Fig. 6E) with AA3+4 vein not bifurcate, AA4 vein missed, AA3 vein connected with Cu vein near apical 1/3 and not extending to margin; CuA2 vein connected with MP3+4 vein near basal 1/3 of MP3+4 vein and not extending to margin; MP3+4 vein bifurcate near apical 1/3, some parts of base of MP3+4 vein missed, a short and vague uncertain vein (?1, either a crossvein or base of MP3+4 vein) connected with base of MP3+4 vein; MP4 vein, MP3 vein and MS vein not extending to margin; a short uncertain vein (?2) located between MP4 vein and MP3 vein, not extending to margin. Abdominal ventrite V raised at apical sides and truncated apically (Fig. 6C).

Male. Unknown.

Etymology

The specific epithet of this new species is derived from the Latin words “niger” and “albus” referring to most of parts of elytral basal half sparsely covered with short, black hairs and most of parts of elytral apical half densely with short, white hairs.

Distribution

Vietnam (Yen Bai).

Diagnosis

This new species can be distinctly distinguished from other species of Trichohoplorana by its peculiar elytral pattern (Fig. 6A).

Remarks

When the senior author received the holotype of this new species, the right antennomere XI was missing and the elytral apex was broken. Then, the head, left antennomere XI, and prothorax were separated from the body due to his carelessness, and he correspondingly glued to the body the separated portions with white emulsoid. Consequently, some hairs on the antennae, elytra, metaventrite, and legs were worn so that some characters are unclear.

Key to species of Trichohoplorana

1 Elytra with a broad transverse white haired band on the middle T. juglandis
Elytra without a broad transverse white haired band on the middle 2
2 Elytra not covered with short white or grayish-white hairs 3
Elytra covered with short white or grayish-white hairs 4
3 Tips of the lateral tubercles of the prothorax obtuse, elytral apex slightly obliquely truncated, with the marginal angle obtuse and not distinctly processed, elytral punctuations fine T. luteomaculata
Tips of the lateral tubercles of the prothorax pointed, elytral apex distinctly obliquely truncated, with the marginal angle pointed and distinctly stretched, elytral punctuations coarse T. shirakii
4 Most of parts of elytra densely covered with grayish-white hairs T. dureli
Most of parts of elytra not densely covered with grayish-white hairs 5
5 Elytra with a yellow haired spot located behind bumps, most of parts of elytral apical half densely covered with short white hairs T. nigeralba
Elytra without a yellow haired spot located behind bumps, most of parts of elytral apical half not densely covered with short, white hairs 6
6 Lateral tubercles of prothorax thick, elytra with a transverse band behind bumps, marginal angles distinctly processed T. mutica
Lateral tubercles of prothorax thin, elytra with a transverse band on the middle, rounded apically T. tenuipes

Acknowledgements

We sincerely appreciate Mr Xavier Gouverneur (CXG) for providing photographs of the holotype of Trichohoplorana luteomaculata and Mimipochira sikkimensis, Dr Andreas Weigel (CWW) for providing a photograph of the holotype of Trichohoplorana dureli, Dr Carolus Holzschuh (CHS) for providing photographs of the type of Trichohoplorana tenuipes. We are very grateful to Andreas Weigel for providing material of T. luteomaculata and literature, to Dr Ping Wang (Yangtze University, Jingzhou, Hubei, China) for providing literature, and to Prof Hong Pang (SYSU), Dr Bing-Lan Zhang (SYSU), and Mr Wei-Cai Xie (SYSU) for providing kind help during the senior author’s visits to SYSU. We express our special appreciation to Mr Ming-Zhi Zhao (South China Agricultural University, Guangzhou, Guangdong, China) for obtaining materials of T. luteomaculata and T. nigeralba. We also thank the reviewers Dr Eduard Vives (Natural Science Museum of Barcelona, Spain), Mr Xavier Gouverneur (Rennes, France), and Dr Francesco Vitali (Academic Editor for Cerambycidae) for improving our manuscript.

This research was supported by Guizhou Provincial Science and Technology Foundation (黔科合基础-ZK[2022]一般527), the Fund Project of the Education Department of Guizhou Province (黔教技[2022]091号, 黔教技[2022]054号, 黔教技[2022]338号), the Science and Technology Innovation Team Project of Liupanshui Normal University (LPSSYKJTD201602).

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