Research Article |
Corresponding author: Lien Thi Phuong Nguyen ( phuonglientit@gmail.com ) Academic editor: Jack Neff
© 2021 Thi Ngat Tran, Lam Xuan Truong, Toshko Ljubomirov, Lien Thi Phuong Nguyen.
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:
Tran TN, Truong LX, Ljubomirov T, Nguyen LTP (2021) First record of the bee genus Bathanthidium (Bathanthidium s. str.) Mavromoustakis (Hymenoptera: Megachilidae) from Vietnam: Description of a new species and a key to species. Journal of Hymenoptera Research 88: 51-60. https://doi.org/10.3897/jhr.88.73969
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The little-known bee genus Bathanthidium Mavromoustakis, 1953 of the family Megachilidae is reported for the first time from Vietnam. A new species, Bathanthidium (Bathanthidium s. str.) paco Tran & Nguyen, sp. nov. from Hoa Binh province is described and illustrated. A nest of the new species is reported from a wooden house. An updated identification key to all known species of the subgenus Bathanthidium s. str. is also provided.
Apoidea, Anthidiini, identification key, morphology, taxonomy
Bathanthidium is a small genus of anthidiine bees occurring in eastern Asia (
In Vietnam, knowledge concerning the taxonomy of the genus Bathanthidium has been extremely limited as the country has been under sampled for bees. We here report this genus for the first time for the Vietnamese fauna, with a species belonging to subgenus Bathanthidium s. str. described as new to science. A nest site of the new species is also described. In addition, an updated key to all recognized species of the subgenus Bathanthidium s. str. is provided.
The materials examined in the present study are deposited in the Hymenopteran collection of the Institute of Ecology and Biological Resources (IEBR), Hanoi, Vietnam. The adult morphological and color characters were examined with a Nikon SMZ745 stereomicroscope. Images were photographed with a Nikon SMZ800N digital stereo microscope, and with ILCE-5000L/WAP2 digital camera attached on that. Photographs were combined with Helicon Focus 7 software to achieve focus stacked images. Finally, all files were processed with Adobe Photoshop CS6.
The morphological terminology used in the description follows
Measurements of body parts follows
The abbreviations S and T (1, 2, 3...) refer to numbered metasomal sterna and terga, respectively.
Subgenus Bathanthidium s. str.: Dianthidium (Bathanthidium) Mavromoustakis, 1953: 837. Type species: Dianthidium bifoveolatum Alfken, 1937, by original designation.
According to
Holotype : Vietnam: ♀, Hoa Binh, Mai Chau, Pa Co, Hang Kia – Pa Co Natural Reserve, 20°44'36"N, 104°53'42"E, alt. 1340 m, Nest#VN-HB-2020-Bath-01, 24 Jun. 2020, Nguyen LTP, Nguyen CQ, Tran NT & Mai TV leg., deposited in IEBR. Paratypes: Vietnam: 2 ♂, same data as holotype, deposited in IEBR.
Based on the presence of fovea behind propodeal spiracle rounded and delimited by strong carina, the new species belongs to subgenus Bathanthidium s. str.
This species can be distinguished from all other known species of subgenus
Bathanthidium s. str. by the following combination of characters: in the both sexes, mandible widened apically, the lowest tooth slightly rounded; in female, clypeus and mandible in entirely black, paraocular area with thin, yellowish-orange marking extending along the inner margin to the top of the eye, scutellum entirely black, T1 with lateral small, dull orange markings, T2–T5 basally with yellowish-orange bands, T1–T2 apically with dull orange bands, the rest of T3–T5 with dull orange to dirty yellow bands, T6 entirely black; in male, T7 of trilobed, median lobe longest and broadest, lateral lobe short, acute and curved inwards, male genitalia large, forked gonostylus with two unequally branches, penis valves with blade shape.
Female (Figs
Head
: In frontal view subcircular, approximately 1.2 times as wide as long (Fig.
A–H Bathanthidium (Bathanthidium s. str.) paco Tran & Nguyen, sp. nov., holotype, female A head in frontal view B mandible in frontal view C propodeum in lateral view, showing the fovea behind propodeal spiracle D mesoscutum and scutellum in dorsal view E fore wing in dorsal view F habitus in dorsal view G habitus in lateral view H nest entrance. Scale bars: 5 mm (H); 1 mm (A, C, E, F, G); 0.5 mm (B, D).
Mesosoma
: Fore wing with two submarginal cells, the first sub-equal in length to second, basal vein nearly straight and meeting Cu vein at acute angle, 2nd m-cu vein exceeding apical margin of the second submarginal cell, stigma nearly twice as long as broad (Fig.
Metasoma
: T1 with carina on basal margin, T6 with margin round apically (Fig.
A–E Bathanthidium (Bathanthidium s. str.) paco Tran & Nguyen, sp. nov., holotype, female A middle tibia in dorso-lateral view, showing the tibial spine B distitarsus of hind leg in frontal view, showing the arolium C metasoma in lateral view D T6 in dorsal view E mesoscutum and scutellum in dorsal view. Scale bars: 1 mm (C, D, E); 0.5 mm (A, B).
Punctation. Clypeus with large, rough and dense punctures, except the apex with small punctures; frons, vertex, and gena with round, large and dense punctures. Mesoscutum with round and dense punctures, size of the punctures smaller and shallower than that on frons. Scutellum with round and dense punctures, size of punctures uneven. T1–T5 with round, small and sparse punctures on basal half and smaller and denser punctures on remain part.
Pubescence. Clypeus, paraocular area and frons with sparse, short and pale white hairs. Mandible with extremely short, brownish-yellow hairs except for some longer hairs at outer margin. Vertex, mesoscutum, scutellum with short, brownish-yellow hairs. S2–S6 with scopa.
Colour. Paraocular area with thin, yellowish-orange marking extending along the inner margin to the top of the eye (Fig.
Male (Fig.
Most characteristics of the male are similar to those of the female, except for the following:
Metasoma
: T7 trilobed, median lobe longest and largest, lateral lobe short, acute and curved inwards (Fig.
Colour. Clypeus yellow, supraclypeal area with small yellow marking, paraocular area with thin, long and yellow to yellowish-orange marking extending along the inner margin to the top of the eye (Fig.
A–I Bathanthidium (Bathanthidium s. str.) paco Tran & Nguyen, sp. nov., paratype, male A head in frontal view B mesoscutum and scutellum in dorsal view C T4–7 in dorsal view D fore wing in dorsal view E abdomen in latero-ventral view F habitus in dorsal view G habitus in lateral view H genitalia in dorsal view I genitalia in ventral view. Scale bars: 1mm (A, B, D, E, F, G); 0.5 mm (C, H, I).
Pubescence. The median part of S3 orange, apical margin of S2–S3 with pale white to dull orange feather combs, S4 shiny on basal half and with short, dense, pale white hairs on remain part and simple hair comb in apical margin, S5 shiny on basal half and short, sparser, pale yellow hairs on remaining part with black, serrated papillae at apical margin (Fig.
This species is most similar to B. (Bathanthidium) bifoveolatum (Alfken, 1937), but can be easily distinguished from the later by the mandible with the lowest tooth slightly rounded in both sexes (mandible with the lowest tooth acute in both sexes of B. bifoveolatum); clypeus entirely black in female (clypeus laterally with yellow markings in female of B. bifoveolatum); mandible basally with dull yellow marking in male (mandible with yellow marking extending from base to nearly top in male of B. bifoveolatum); mesoscutum latero-anteriorly with small faint yellowish-orange spots or absent, scutellum, pronotal lobe black in both sexes (mesoscutum anteriorly and scutellum apically with thin and long yellow marking interrupted medially; pronotal lobe with yellow marking basally in both sexes of B. bifoveolatum); T2 with yellowish-orange entirely bands, not interrupted medially in both sexes (T2 laterally with yellow markings in both sexes of B. bifoveolatum).
A nest was discovered in a wooden plank in the door of a house, the entrance hole of the nest with a diameter of about 4 mm (Fig.
Northern Vietnam (Hoa Binh province).
(Based on
1 | Flagellum 10–segmented, female | 2 |
– | Flagellum 11–segmented, male | 5 |
2 | Paraocular area with thin and long yellow or yellowish-orange marking extending along the inner margin to the top of the eye | 3 |
– | Paraocular area near ventral extreme with a small sub-triangle or sub-rectangle dull yellow marking | 4 |
3 | Mandible with the lowest tooth acute (see fig. 34 in |
B. (Bathanthidium s. str.) bifoveolatum (Alfken, 1937) |
– | Mandible with the lowest tooth slightly rounded (Fig. |
B. (Bathanthidium s. str.) paco, sp. nov. |
4 | T2 entirely black, T3–T5 with yellow bands, the band on T3 obviously interrupted medially (see fig. 2d in |
B. (Bathanthidium s. str.) fengkaiense Niu & Zhu, 2019 |
– | T2 with a pair of small, stripe-like yellow markings medially, T3–T5 with broader yellow bands, not interrupted medially (see fig. 12 in |
B. (Bathanthidium s. str.) hainanense Niu, Wu & Zhu, 2012 |
5 | Mandible with yellow marking extending from base to nearly top (see fig. 39 in |
B. (Bathanthidium s. str.) bifoveolatum (Alfken, 1937) |
– | Mandible basally with dull yellow marking (Fig. |
B. (Bathanthidium s. str.) paco, sp. nov. |
Bathanthidium has a primarily Indomalayan distribution with almost all the described species (except B. malaisei from South Korea, and depending on whether or not one considers B. emeiense and B. bicolor to occur in Indomalaya) occuring in this biogeographic realm, the majority having been reported from southern China. The discovery of B. paco in northern Vietnam is both consistent with this pattern and extends the range of Bathanthidium.
Very little is known of the biology of Bathanthidium. The only description of a nest of any Bathanthidium is that of
The authors would like to thank the subject editor, Jack Neff, and an anonymous reviewer for their valuable comments to improve the draft quality. We are also sincerely thank the Director (Mr. Luong Thanh Nguyen) and staffs (Mr. Khanh Tien Nguyen and Mr. Cong Van Bui) of Hang Kia – Pa Co Natural Reserve for providing support and permission. The present study was supported by the Vietnam Academy of Science and Technology under two grants (ĐLTE00.04/22-23 and QTBG01.01/21-22).