Biodiversity Data Journal :
Taxonomy & Inventories
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Corresponding author: Zhenhua Liu (liuzhh_beetle@giz.gd.cn), Bi Ding (524097262@qq.com)
Academic editor: Cheng-Bin Wang
Received: 17 Oct 2024 | Accepted: 15 Nov 2024 | Published: 27 Nov 2024
© 2024 Jia-Xiao Sun, Zhenhua Liu, Bi Ding, Rongxiang Su, Guanmin Huang, Zhiyong Xue
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Sun J-X, Liu Z, Ding B, Su R, Huang G, Xue Z (2024) Contribution to the tribe Apalochrini (Coleoptera, Melyridae, Malachiinae) of China, with notes on the genus Dicranolaius Champion and Intybia Pascoe. Biodiversity Data Journal 12: e139509. https://doi.org/10.3897/BDJ.12.e139509
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Apalochrini is a tribe of the family Melyridae characterised by the shortened pedicel, with 13 genera recorded in China at present. Dicranolaius Champion and Intybia Pascoe of Apalochrini are distributed in Asia and Southeast Asia, with the former genus extending to Australia, but not being found in China. In a recent expedition in the mangrove forests of Zhangzhou City (Fujian Province), eastern China, specimens of D. mangalicola Asano & Kawashima, 2010 and I. swatowensis (Wittmer, 1956) were collected.
Dicranolaius Champion is recorded from China for the first time and I. swatowensis is newly recorded for Fujian Province. Diagnostic characters of D. mangalicola is provided and I. swatowensis is re-described in details. An updated key to genera of the Chinese Apalochrini, based on male characters, is given.
soft-winged flower beetles, mangrove forests, new record, Fujian
Melyridae is a family within the superfamily Cleroidea of Coleoptera, consisting of three subfamilies, over 300 genera and 6000 species cosmopolitanly (
The genus Dicranolaius includes over 90 species from Oriental and Australian areas, with most species distributed on Australia, only 13 species being known from East and Southeast Asia (
In this study, D. mangalicola and I. swatowensis are illustrated with colour images and the later species is re-described, based on the newly-collected specimens.
Materials examined in this study are deposited in the following institutions:
Specimens for dissections were softened in hot water for about 10 minutes and the abdomen was removed to a glass dish with 5% solution of potassium hydroxide (KOH) for about 12 hours to clear the muscles. Dissections of male genitalia were done on open slides with glycerine on it using fine dissecting needles. Layered images were captured using the Canon 7D DSLR camera mounted on a Wemacro Focus Stacking Rail, with Canon MPE-65 mm macro lens, Mitutoyo 5× and 10× objective lens and dual-headed flash, with the help of Helicon Remote (v. 3.9.10 M) and WeMacro Control software. The images were then stacked in Helicon Focus v. 8.1.1 and edited in Photoshop CC 2022. The terminologies used in this paper follow Lawrence and Ślipiński (2013). Measurements were made with the following standards: body length-from apical edge of clypeus to apex of elytra; pronotal length-median line from anterior margin to posterior margin; pronotal width-maximum width of pronotum; elytral length-from base of scutellum to elytral apex along suture; elytral width-maximum width across the elytra.
This species can be easily recognised from the congeners by colour patterns on the elytron, with a large arcuate whitish marking open to the lateral margin at base, a small yellow spot on humeral area surrounded by the arcuate marking and a large whitish spot on subapical area (Fig.
China: Fujian (new record for China); Japan.
The habitat is mangrove forest (Fig.
This species can be distinguished from the other species of Intybia mainly by the shapes of antennomere 3 (Fig.
Intybia swatowensis (Wittmer, 1956). A male, dorsal view; B male, ventral view; C female, dorsal view; D male antenna, lateral view; E male antenna, dorsal view; F elytra; G male genitalia, ventral view; H pygidium (apical tergite); I ultimate abdominal ventrite (apical sternite); J anterior tarsi, male. Scale bars: 1.0 mm (A-C).
China: Guangdong, Fujian (new record for Fujian).
Specimens of I. swatowensis are mostly found on leaves or rocks far away from the coast (personal observation by Zhenhua Liu), but was also collected in mangrove forests in this study (Fig.
Male. Length 2.9-3.5 mm. Head and prothorax black, with a quadrate orange spot on frons; antenna with basal 3 segments orange, scape with dorsal surface dark, remaining segments brown to dark brown. Elytra black with metallic bluish lustre, with an orange band across suture before middle. Legs black, anterior tarsi of male lacking comb above the 2nd tarsomere. Abdomen black with median area orange. Vestiture double of dense short setae and much sparser longer bristles.
Head. Head narrower than pronotum; dorsal surface nearly smooth, depressed behind eyes, forming a carina from temple area to ventral side. Eyes elliptical and prominent laterally. Antenna with scape and antennomere 3 expanded and laterally flattened; scape sub-triangular with outer surface slightly depressed; antennomere 3 sub-rectangular, distinctly depressed on outer surface, with a membranous projection near base.
Thorax. Pronotum about 0.9 times as long as wide, lateral margins distinctly constricted at base; disc area smooth, only with a few punctations on lateral areas posteriorly, transversely depressed near base. Prosternum short, prosternal process highly reduced. Procoxal cavities large and transverse, contiguous at middle; procoxae distinctly projecting. Mesoventrite small and shield-shaped, mesepisternum and mesepimeron large. Metaventrite about as long as wide, slightly dilated. Mesocoxae triangular and projecting, meeting at middle. Metacoxae narrowly separated, abruptly narrowed to lateral. Legs relatively slender, with femora slightly enlarged near base, tarsal formula 5-5-5, anterior tarsi without comb on tarsomere 2 (Fig.
Elytra. Oblong-ovate, widest at about posterior third, about 1.5 times as long as wide; dorsal surface shiny, with sparse coarse punctations mostly on median areas and denser fine punctations between and next to them; vestiture mostly dark, which are yellowish on orange band.
Abdomen. With 6 ventrites, gradually narrowing to posterior; ventrite 1 divided at middle, only visible at lateral. Tergite VIII sub-trapezoid, with posterior margin arcuate; sternites VIII nearly divided, with median area membranous. Male genitalia with penis broadly rounded apically, inner sac with a long sclerotised flagellum and numerous tiny spines apically.
Female. Similar to male on body shape and colouration, but head with dorsal surface entirely black, antenna with scape and antennomere 3 only elongated.
Updated key to genera of the Chinese Apalochrini (male only) ( |
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1 | Antenna with scape and antennomere 3 dilated and modified | 2 |
– | Antenna with basal antennomeres simple | 8 |
2 | Front tarsi 4-segmented | Platyintybia Liu, 2024 |
– | Front tarsi 5-segmented | 3 |
3 | Front tarsi without comb on tarsomere 2 | 4 |
– | Front tarsi with comb on tarsomere 2 | 6 |
4 | Front tibiae thickened and curved, with concavity at base | Laius Guérin-Méneville, 1831 |
– | Front tibiae simple | 5 |
5 | Body shape ant-like, with prothorax elongated and distinctly constricted posteriorly, elytra constricted at base | Myrmecospectra Motschulsky, 1858 |
– | Body shape not ant-like, prothorax never distinctly longer than wide, elytra with humeral area not distinctly constricted | Intybia Pascoe, 1866 |
6 | Head with a deep hollow or protuberance, antennomere 3 dilated, but without bunch of hairs | Troglocollops Wittmer, 1965 |
– | Head with interocular area flat | 7 |
7 | Antennomere 3 dilated and with bunch of hairs | Protocollops Evers, 1991 |
– | Antennomeres 3 dilated, without bunch of hairs | Dicranolaius Champion,1921 |
8 | Metathorax slightly convex, not protruding, simple and lacking appendages or tufts of hairs | 9 |
– | Metathorax convex and bears horn-like appendage | 13 |
9 | Abdomen with aculeiform appendage on 4th and 5th sternites | 10 |
– | Abdomen simple, lacking appendages | 11 |
10 | Intermediate tibiae slightly widened and excavated on inner side, anterior trochanters simple | Opisthapalochrus Evers, 1987 |
– | Intermediate tibiae simple, not widened, anterior trochanters dentate | Spinapalochrus Pic, 1919 |
11 | Anterior tibiae emarginate in dorsal side, intermediate tibiae strongly dilate and convex | Hadrocnemus Kraatz, 1895 |
– | Legs simple, not emarginate or dilated | 12 |
12 | Anterior tarsi with a comb above second tarsomere. Antennae flabellate, vestiture covered with double pubescence, white and black | Pectapalochrus Tshernyshev, 2016 |
– | Anterior tarsi without a comb above second tarsomere. Antennae filiform, vestiture covered with dark pubescence | Apalochrus Erichson, 1840 |
13 | Eyes extremely large, elytra impressed apically, pygidium (apical tergite) evenly rounded distally and with specifically sculptured concave-caliciform apex | Mimapalochrus Tshernyshev, 2015 |
– | Eyes and elytral apices simple, not enlarged or impressed, pygidium (apical tergite) emarginate in the middle and not sculptured | Dromanthomorphus Pic, 1921 |
Within the 51 genera of Melyridae recorded in China before this study (
Though Intybia swatowensis was also collected in mangrove forests, it is more commonly found on leaves or rocks far away from coast (personal observation by Zhenhua Liu). Thus, it is apparently not restricted to a simplex habitat as are the other two species mentioned above.
This study was supported by the Forestry Science and Technology project of Fujian Province (no.2023FKJ19), Science and Technology planning project of Fujian Province (no. 2023R1051), National Natural Science Foundation of China (no. 32200374), GDAS Special Project of Science and Technology Development (2022GDASZH-2022010106), the Key Laboratory of State Forestry and Grassland Administration on Timber Forest Breeding and Cultivation for Mountainous Areas in Southern China and the Fujian Key Laboratory of Forest Cultivation and Forest Products Processing and Utilization.
We thank Dr. Haitian Song (Fujian Academy of Forestry) for field collecting and providing suggestions for the manuscript. Various fieldwork assistance provided by the Zhangjiangkou Mangrove Forestry National Nature Reserve and the Longhai Mangrove Forestry Nature Reserve was greatly appreciated. We would also like to thank Dr. Isidor Plonski, Dr. Sergei Tshernyshev and Dr. Cheng-Bin Wang for their comments, helping to greatly improved our manuscript.