Translator Disclaimer
1 January 2020 Charaea luzonicum sp. nov. (Coleoptera: Chrysomelidae: Galerucinae): the first record of Charaea in the Philippines
Jan Bezděk
Author Affiliations +
Abstract

The first representative of the genus CharaeaBaly, 1878, Ch. luzonicum sp. nov., is described from Luzon Island, the Philippines. Based on the characteristic internal sclerites of the aedeagus, the new species belongs to the Ch. coomani species group. Colour photos and drawings of habitus and both male and female genitalia are presented.

INTRODUCTION

The taxonomy and geographic distribution of the genus Charaea are insufficiently known. The main reason is a long and complicated history of taxonomic research of the genus Charaea (see Bezděk & Lee, 2014). The species were dispersed in various genera (predominantly in Calomicrus Dillwyn, 1829 and Exosoma Jacoby, 1903) and cummulated to Charaea just in several last years (Beenen & Warchałowski, 2010; Bezděk, 2012; Bezděk & Lee, 2014). Taphinellina Maulik, 1936, usually treated as synonym of Charaea, is not congeneric and its taxonomic position will be clarified in the near future (Bezděk, submitted). Recently, Charaea was synonymized either with Calomicrus or Exosoma (see Medvedev & Sprecher-Uebersax, 1998; Kimoto, 2004) but these acts were unwarrented and not followed by subsequent authors as Calomicrus and Exosoma are morphologically and partly also geographically remarkably different. Last year, the genus Charaea was redescribed, clarified as valid genus and compared with similar genera (Bezděk & Lee, 2014).

Currently, 44 species distributed in the eastern Palaearctic, Himalayas, China and adjacent countries of the Oriental Region are classified in Charaea. However, some transfers from other genera are still expected and at least 20 new species are waiting for being described. During a two weeks stay in Naturhistoriska Riksmuseet Stockholm within the frame of Synthesys (SE-TAF-3534), I examined several tens of species originating from the Philippines and named by the German coleopterist Julius Weise (1844-1925) but never described, including those provided with the unpublished manuscript name Calomicrus luzonicus. The specimens belong to Charaea and represent the first known Charaea specimens from the Philippines. Although the distribution of the genus Charaea was significantly extended last year, the discovery of the new species in the Philippines is really surprising and suggests a much wider distribution than expected as there is so far no confirmed occurence of the genus Charaea in the Sunda islands of Malaysia and Indonesia.

MATERIAL AND METHODS

All measurements were made using an ocular grid mounted on MBS-10 stereomicroscope (at 16× magnification for the body length and 32× magnification for the remaining measurements). Photographs of specimens were taken with Canon EOS 550D digital camera with Canon MP-E 65 mm objective. Images of the same objects at different focal planes were combined using Helicon Focus 5.1.3 software.

The aedeagus was soaked overnight in cold 10% KOH solution, washed in water and an entomological pin was moved through the basal orifice to push the internal sac through the dorsal opening. The aedeagus with everted sac was put into a depression slide filled with glycerol, covered by a cover slip and photographed. The aedeagus was then put into a microvial with glycerol attached to the pin with the specimen. Subsequently, the figures were edited with Corel Photopaint 12.

TAXONOMY

Genus Charaea Baly, 1878

  • Charaea Baly, 1878: 376 (type species Charaea flaviventre Baly, 1878, by monotypy).

  • Taphinellina Maulik, 1936: 299 (type species Taphinella bengalensis Jacoby, 1900, by original designation).

  • Charaea luzonicum Bezděk sp. nov.
    Figs 1-10

  • Holotype: NHRS-JLKB 000023081; male; Mt. Banahao; P. I. Baker leg.

  • Paratypes: NHRS-JLKB 000023079; male; Mt. Banahao; P. I. Baker leg. – NHRS-JLKB 000023082; female; Mt. Banahao; P. I. Baker leg. – NHRS-JLKB 000023080; female; Mt. Banahao; P. I. Baker leg. – NHRS-JLKB 000023083; female; Mt. Banahao; P. I. Baker leg. – NHRS-JLKB 000023085; Baguio, Benguet; P. I. Baker leg.

  • The specimens are provided with one additional red label: HOLOTYPUS, [or PARATYPUS], Charaea luzonicum sp. nov., J. Bezděk det., 2014. All the specimens are deposited in Naturhistoriska Riksmuseet Stockholm (Sweden).

  • Diagnosis: Due to a diagnostic structure of the aedeagus and particularly the internal sac with long clavate lateral sclerites, Charaea luzonicum sp. nov. belongs to the Ch. coomani group as tentatively defined by Bezděk & Lee (2014). Currently, the group contains 4 species: Ch. coomani (Gressitt & Kimoto, 1963) (Vietnam), Ch. hainanicum (Gressitt & Kimoto, 1963) (China: Hainan), Ch. mimicum (Medvedev, 1998) (Taiwan) and Ch. kelloggi (Gressitt & Kimoto, 1963) (Taiwan, Hongkong, China: Fujian, Guizhou, Guangdong).

  • A male of Ch. hainanicum was not available for this study, but the apex of its aedeagus is widely obtusangulate (Fig. 12) based on the drawing in the original description, while it is concave in Ch. luzonicum sp. nov. (Fig. 10). From the other three species, Charaea luzonicum sp. nov. can be distinguished by wider pro- and mesotarsomeres I (other species in Ch. coomani group have also parallel pro- and mesotarsomeres I but slenderer), shorter subapical antennomeres (2.2 times as long as wide in Ch. luzonicum sp. nov. while 2.5 times in Ch. kelloggi and 3 times in Ch. coomani and Ch. mimicum), an aedeagus not prolonged apically and its ventral side with shallow median impression (aedeagus with more or less prolonged apex and without impression in Ch. kelloggi, Ch. coomani and Ch. mimicum) (cf. Figs 10-14), the outer sides of lateral sclerites in aedeagus with fine denticulations (Fig. 7; smooth in Ch. kelloggi and Ch. mimicum, not studied in Ch. coomani).

  • Etymology: Derived from Luzon Island where the type series was collected.

  • Description: Dorsal side glabrous, oval, convex. Colour metallic bluish-black, abdomen yellowish brown, mandibles brown with black apices, labrum metallic with brownish anterior margins, antennae black with antennomeres I-III brownish, legs metallic with brownish knees.

  • Male (holotype, Fig. 1). Labrum transverse, with six pores in transverse row bearing pale seta, with rounded and convergent lateral margins, anterior margin emarginate in middle. Anterior part of head nearly impunctate, lustrous, with several long setae on anterior margin of clypeus, along lateral margins of nasal keel and along anterior margins of antennal sockets. Nasal keel wide, moderately convex. Interantennal space 1.8 times as wide as transverse diameter of antennal socket. Frontal tubercles large, subtriangular, elevated, lustrous, glabrous, impunctate, anterior tips divergent, separated by nasal keel. Interocular space wide, 2.2 times as wide as transverse diameter of eye. Vertex separated from frontal tubercles by deep furrow, impunctate, behind each eye with several long setae. Antennae filiform, 0.55 times as long as body, length ratio of antennomeres equals 12-5-6-10-10-10-10-10-11-11-15, antennomeres I–III lustrous, covered with sparse setae, antennomeres IV-XI dull, covered with dense short setae.

  • Pronotum lustrous, 1.3 times as broad as long, widest in middle, moderately convex, covered with double punctures (smaller and larger). Anterior margin nearly straight, unbordered, lateral margins rounded with broad border, posterior margin straight in middle, lateral parts rounded, thinly bordered. Anterior angles distinctly swollen, rectangular, posterior angles with small pointed tip. All angles with setigerous pore bearing long pale seta, additional short setae visible on lateral margins of pronotum.

  • Scutellum subtriangular with widely rounded tip, impunctate, glabrous.

  • Elytra 1.6 times as long as wide and 0.6 times as long as body, widest behind middle, almost glabrous (with very scarse short pale setae on apical slopes), densely covered with fine small confused punctures. Humeral calli well developed. Epipleura impunctate, wide basaly, gradually narrowing and disappearing before apex. Macropterous. Anterior coxal cavities opened posteriorly. Prosternal process thinly visible but not elevated between procoxae. Ventral surface lustrous, sparsely covered with fine punctures and pale setae, metepisterna dull, covered with dense setae. Abdomen with last ventrite transverse, posterior margin with two short subtriangular incisions, median lobe slightly concave (Fig. 6).

  • Legs slender. All tibiae with apical spur in both sexes. Length ratio of protarsomeres I, II, III and V equals 9-6-5-11, protarsomere I robust, parallel, 1.8 time as long as wide; length ratio of mesotarsomeres I, II, III and V equals 11-9-5-12, mesotarsomere I robust, subparallel, with lateral margins shallowly widely concave, 2.2 time as long as wide; length ratio of metatarsomeres I, II, III and V equals 12-8-5-12, metatarsomere I elongate triangular, 2.4 times as long as wide. Claws appendiculate.

  • Aedeagus symmetrical, subtubular, parallel subapicaly, basal half slightly convergent, apical part convergent with tip concave, ventral side with shallow furrow in apical half (Figs 2, 10). Internal sac with three sclerites: very slender median sclerite and pair of lateral sclerites which are flat, subclavate, with outer lateral side covered with fine denticulations. Median sclerite is slightly longer than lateral ones (Figs 3, 7).

  • Female: Interocular space slightly wider, 2.55 time as wide as transverse diameter of eye. Protarsomere I and mesotarsomere I not parallel but elongate triangular. Last ventrite transverse with posterior margin widely shallowly concave (Fig. 4). Pygidium transverse, widely rounded (Fig. 5). Sternite VIII (Fig. 9) subtriangular with anterior margin shallowly concave in middle, laterally oblique, lateral margins slightly rounded towards tignum, short setae are cummulated along posterior margin, tignum slender, twice longer than sternite VIII, apically bent. Spermatheca: nodulus poorly delimited, elongate, slightly wider than cornu, cornu shortly C-shaped with inner angle sharp, apex with indicated appendix, proximal spermathecal duct robust, slightly S-shaped (Fig. 8).

  • Dimensions: Males: 4.3-5.3 mm (holotype 5.3 mm), females: 4.7-5.3 mm.

  • Distribution: Philippines (Luzon Isl.).

  • Type locality: Philippines, Luzon, Banahao Mt. [14°03′53″N 121°28′47″E].

  • Figs 1-3.

    Charaea luzonicum sp. nov. (1) Habitus (male, holotype, 5.2 mm). (2)Transmitted light illumination of aedeagus in dorsal view, internal sac not everted. (3) Aedeagus with everted internal sac (a - dorsal, b - lateral, c - ventral view). Not to scale.

    f01_371.jpg

    Figs 4-9.

    Charaea luzonicum sp. nov. (4) Female last ventrite. (5) Female pygidium. (6) Male last ventrite. (7) Right lateral sclerite in aedeagus. (8) Spermatheca. (9) Sternite VIII. Scale bars: 0.5 mm for Figs 4-6, 0.25 mm for Figs 8-9.

    f04_371.jpg

    Figs 10-14.

    Aedeagus (a - dorsal, b - lateral, c - ventral view). (10) Charaea luzonicum sp. nov. (11) Ch. coomani. (12) Ch. hainanicum (based on Gressitt & Kimoto, 1963). (13) Ch. kelloggi. (14) Ch. mimicum. Scale bar: 0.5 mm.

    f10_371.jpg

    ACKNOWLEDGEMENTS

    This research received support from the Synthesys Project SE-TAF-3534 ( http://www.synthesys.info/) financed by the European Community - Research Infrastructure Action under the Seventh Framework Programme. Special thanks are due to Johannes Bergsten for his assistance in the collections during my stay in Naturhistoriska Riksmuseet Stockholm.

    REFERENCES

    1.

    Baly J.S. 1878. Descriptions of the phytophagous Coleoptera collected by the late Dr. F. Stoliczka during Forsyth's expedition to Kashgar in 1873-74. Cistula Entomologica 2(1875-1882): 369-383. Google Scholar

    2.

    Beenen R., Warchałowski A. 2010. Charaea pseudominutum n. sp., an undescribed but not unknown galerucine beetle (Coleoptera, Chrysomelidae, Galerucinae). Entomolo-gische Blätter 106: 57-62. Google Scholar

    3.

    Bezděk J. 2012. Taxonomic and faunistic notes on Oriental and Palaearctic Galerucinae and Cryptocephalinae (Coleoptera: Chrysomelidae). Genus 23: 375-418. Google Scholar

    4.

    Bezděk J. submitted. Redescription and identity of Taphinella bengalensis Jacoby, 1900 (Coleoptera: Chrysomelidae: Galerucinae). Turkish Journal of ZoologyGoogle Scholar

    5.

    Bezděk J., Lee Ch.-F. 2014. Revision of Charaea (Coleoptera: Chrysomelidae: Galerucinae) from Taiwan. Zootaxa 3861: 1-39. Google Scholar

    6.

    Dillwyn L. W. 1829: Memoranda relating to coleopterous insects found in the neighbourhood of Swansea. W. C. Murray and D. Rees, Swansea, 75 pp. Google Scholar

    7.

    Gressitt J.L., Kimoto S. 1963. The Chrysomelidae (Coleopt.) of China and Korea, part 2. Pacific Insects Monograph 1(B): 301-1026. Google Scholar

    8.

    Jacoby M. 1900. New species of Indian phytophaga principally from Mandar in Bengal. Mémoires de la Société Entomolo-gique de Belgique 7: 95-140. Google Scholar

    9.

    Jacoby M. 1903. A further contribution to our knowledge of African phytophagous Coleoptera, part II. The Transactions of the Entomological Society of London 1903: 1-38. Google Scholar

    10.

    Kimoto S. 2004. New or little known Chrysomelidae (Coleoptera) from Nepal, Bhutan and the northern territories of Indian subcontinent. Bulletin of the Kitakyushu Museum of Natural History and Human History, Series A (Natural History) 2: 47-63. Google Scholar

    11.

    Maulik S. 1936. The fauna of British India including Ceylon and Burma. Coleoptera, Chrysomelidae (Galerucinae). Taylor and Francis, London, XV + 648 pp. Google Scholar

    12.

    Medvedev L.N. 1998. New Chrysomelidae (Coleoptera) from Southeast Asia in the Hungarian Natural History Museum. Annales Historico-Naturales Musei Nationalis Hungarici 90: 163-174. Google Scholar

    13.

    Medvedev L.N., Sprecher-Uebersax E. 1998. New data on Chrysomelidae of Nepal (Insecta, Coleoptera). Spixiana 21: 25-42. Google Scholar
    Jan Bezděk "Charaea luzonicum sp. nov. (Coleoptera: Chrysomelidae: Galerucinae): the first record of Charaea in the Philippines," Revue suisse de Zoologie 122(2), 371-375, (1 January 2020). https://doi.org/10.5281/zenodo.30005
    Accepted: 28 April 2015; Published: 1 January 2020
    JOURNAL ARTICLE
    5 PAGES


    SHARE
    ARTICLE IMPACT
    Back to Top