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New records of Celaenorrhinus pyrrha de Nicéville, 1889 and C. munda (Moore, 1884) from China (Lepidoptera, Hesperiidae)
expand article infoGuo-Xi Xue, Yutaka Inayoshi§, Meng Li, Fu-Ming Zhang|, Da-Kun Lai|, Hai-Ying Tian
‡ Zhengzhou University of Light Industry, Zhengzhou, China
§ Sritana Condominium, Chiang Mai, Thailand
| Forest Resource Service Center of Simian Mountain, Chongqing, China
¶ China Tobacco Henan Industrial Co., Zhengzhou, China
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Abstract

Celaenorrhinus pyrrha de Nicéville, 1889, a rare species of Hesperiidae previously known to be distributed from northeastern India to Indochina, is reported from southwestern Yunnan and southwestern Chongqing, China. A 658 bp COI gene sequence of this species is published for the first time. Although Chongqing is obviously isolated from the main distribution range, morphological characters of the specimens from this locality do not indicate a subspecies differentiation. Another rare taxon, C. munda munda (Moore, 1884), is also recorded from China for the first time based upon a male specimen from Cuona County in the Tibet Autonomous Region. This is the second specimen of C. munda from China, over 100 years after the holotype of C. munda joka Evans, 1949. The genitalia of both species are illustrated and described. Some taxonomic notes and a distribution map are provided as well.

Keywords

COI, distribution, fauna, female genitalia, male genitalia, subspecies

Introduction

The genus Celaenorrhinus Hübner, [1819] includes over 100 species worldwide (Evans 1949; Yuan et al. 2015). In China, 23 species of the genus have been recorded, most of which are distributed in southern China (Wu and Hsu 2017). In this paper, two rare taxa of the genus are added to the Chinese skipper fauna, viz. C. pyrrha de Nicéville, 1889 and C. munda munda (Moore, 1884).

Celaenorrhinus pyrrha is known from Sikkim, Bhutan through Assam to Indochina (Evans 1949; Eliot 1959; Osada et al. 1999; Kimura et al. 2011; Ek-Amnury 2012; Nakamura and Wakahara 2012; Monastyrskii and Devyatkin 2015). In the present study, it is reported from southwestern Yunnan and southwestern Chongqing in China.

Celaenorrhinus munda was recorded from China by Evans (1949) as the subspecies C. munda joka Evans, 1949, a subspecies based on a single specimen captured from northwestern Yunnan in 1898. No additional material of this species had been found in China since. In the present study, a male specimen of C. munda munda is reported from southern Tibet as the easternmost record of this subspecies and the second specimen of C. munda from China.

Since the genitalia structures of Celaenorrhinus pyrrha and C. munda have not been illustrated in detail except for the simple hand drawings by Evans (1949: pl. 16, B.6., fig. 8; pl. 17, B.6. fig. 19), the genitalia of both taxa are illustrated and described herein. A 658 bp COI sequence of C. pyrrha is also provided for DNA barcoding and future molecular studies.

Materials and methods

Morphological examination

9♂♂, 7♀♀ of Celaenorrhinus pyrrha and 1♂ of Celaenorrhinus munda munda were studied. Specimens from China are deposited in Zhengzhou University of Light Industry, and those from Thailand and Vietnam are in the private collections of Mr. Kotaro Saito (Tokyo) and Mr. Yutaka Inayoshi (Chiang Mai). Detailed information for each specimen can be found in the Results under each species.

The terminology of morphology mainly follows those of Evans (1949), Klotz (1970) and Yuan et al. (2015).

The genitalia of both sexes were examined in glycerin and photographed using an Olympus SZX7 stereomicroscope after clearing in a cold 10% NaOH solution. Images were taken with a Canon PowerShot G16 digital camera. Image post-processing was accomplished with Adobe Photoshop CS 8.0.1.

DNA extraction and sequence analysis

One leg of each dried specimen (Table 1) was used to extract genomic DNA following the protocol provided by DNeasy Blood and Tissue Kit (Qiagen, Germany). The partial COI gene of 658 bp was amplified by PCR using the universal primer pairs LepF and LepR, as described by Hajibabaei et al. (2006). The PCR reactions were performed in a 20 µL mixture containing 2 µL genomic DNA, 10 µL 2×Taq mix (Vazyme Biotech, China), and 0.5 µL (10 µM) forward and reverse primers. The amplification cycle was preheating at 94 °C for 3 min, then 30 cycles of 94 °C for 1 min, 50 °C for 45 sec, and 72 °C for 1 min, and a final step of 72 °C for 10 min. The PCR products were directly sequenced by Sunya Biotech, Zhengzhou, China. Multiple sequence alignments were performed in Clustal X 2.0.12 with default parameters (Thompson et al. 1997). The creditability of COI sequences was verified by BLAST and sequences were then submitted to GenBank in NCBI.

Table 1.

Specimens used for sequencing and molecular analysis.

Species Locality Date Sex Voucher ID Accession number
Celaenorrhinus pyrrha China, Yunnan, Yingjiang, Jinzhuzhai 27.IV.2016 male A56 MT997273
China, Chongqing, Simian Mountain 16.VIII.2016 male A57 MT997274
China, Chongqing, Simian Mountain 16.VIII.2016 male A58 MT997275
China, Chongqing, Simian Mountain 16.VIII.2016 female A59 MT997276
China, Chongqing, Simian Mountain 16.VIII.2016 female A60 MN443912
Celaenorrhinus macrostictus Gabon, MDC Lonmin 29.I.2008 male JN277521.1*
Celaenorrhinus dargei Nigeria, Obudu Plateau 11.IV.2007 KP149680.1*
Celaenorrhinus patula China, Tibet, Motuo VII.2018 SCAU He1657 MN199383.1*

COI sequences of Celaenorrhinus macrostictus, C. dargei and C. patula (Table 1) were downloaded from GenBank as outgroups for the phylogenetic analysis. The software MEGA 7.0.26 (Kumar et al. 2016) was used to calculate the Kimura-2-Parameter distance and reconstruct a neighbor-joining (NJ) tree. Node support values were estimated with 1000 bootstraps replicates.

Results

Celaenorrhinus pyrrha de Nicéville, 1889 (new record to China)

Figs 1–3

Celaenorrhinus pyrrha de Nicéville, 1889: 181. Type locality: Bhutan; Evans 1949: 95; Eliot 1959: 383; Osada et al. 1999: 188; Kimura et al. 2011: 33; Ek-Amnury 2012: 798; Nakamura and Wakahara 2012: 57; Monastyrskii and Devyatkin 2015: 72.

Material examined

Material dissected and sequenced: 1♂ 1♀, China, Chongqing, Simian Mountain, 785 m, 16 August 2016, leg. Guoxi Xue [Dissection ID CQ164, CQ165; DNA voucher ID A58, A59]; 1♂, China, Yunnan, Yingjiang, Jinzhuzhai, 27 April 2016, leg. Guoxi Xue [Dissection ID YN25, DNA voucher ID A56]. Material dissected: 1♂ 1♀, China, Chongqing, Simian Mountain, 17 June 2007, 23 September 2007, 500–1,000 m [Dissection ID CQ125, CQ67]; 1♂ 1♀, Thailand, Nan, Doi Phu Kha, 4, 18 October 1991, leg. Inayoshi Yutaka [Dissection ID Th1, Th2]. Material sequenced: 1♂ 1♀, China, Chongqing, Simian Mountain, 785 m, 16 August 2016, leg. Guoxi Xue [DNA voucher ID A57, A60]. Other material examined: China • 1♀, Chongqing, Simian Mountain, 785 m, 16 August 2016, leg. Guoxi Xue; 2♀♀, Chongqing, Simian Mountain, 17 June 2007, 23 September 2007, 500–1,000 m. Vietnam • 1♂, Lam Dong Province, near Dalat City, Nong Trai, 1,200 m, 16 August 2003, leg. Kotaro Saito; 1♂, Dalat City, Nong Trai, 10 September 2008, leg. T. Saito; 2♂♂, Dalat City, Nong Trai, 1,200 m, 12 April 2009, 24 May 2009, leg. Kotaro Saito.

Figures 1–4. 

Adults of Celaenorrhinus pyrrha and C. munda munda. 1–3 C. pyrrha 1 male, China, Chongqing, Simian Mountain, 785 m, 16 August 2016, leg. Guoxi Xue [Dissection ID CQ164, DNA voucher ID A58] 2 male, China, Yunnan, Yingjiang, Jinzhuzhai, 27 April 2016, leg. Guoxi Xue [Dissection ID YN25, DNA voucher ID A56] 3 female, China, Chongqing, Simian Mountain, 785 m, 16 August 2016, leg. Guoxi Xue [DNA voucher ID A60] 4 C. munda munda, male, China, Tibet, Cuona County, Lebugou, 19 June 2013, leg. Songyun Lang [Dissection ID Tib1] a dorsal side b ventral side. Scale bars: 1 cm.

Molecular analysis

A 658 bp partial COI sequence was successfully generated from each specimen used for DNA extraction (Table 1) via PCR and sequencing. The alignment of all the sequences used to perform a phylogenetic analysis is provided in Suppl. material 1. In the NJ tree (Fig. 5), the five voucher specimens were clustered into one clade, within which the mean K-2-P distance is 0 (Table 2), indicating they belong to the same species.

Table 2.

Uncorrected pairwise genetic distances (Kimura-2-parameter) for the COI sequences of Celaenorrhinus species.

1 2 3 4 5 6 7
1. MT997273_A56
2. MT997274_A57 0.000
3. MT997275_A58 0.000 0.000
4. MT997276_A59 0.000 0.000 0.000
5. MN443912_A60 0.000 0.000 0.000 0.000
6. MN199383.1 0.082 0.082 0.082 0.082 0.082
7. JN277521.1 0.075 0.075 0.075 0.075 0.075 0.089
8. KP149680.1 0.078 0.078 0.078 0.078 0.078 0.075 0.043
Figure 5. 

NJ tree based on Kimura-2-Parameter distances for the partial mitochondrial COI sequences of Celaenorrhinus, values at nodes represent the bootstrap support (BP) values.

Description

Male genitalia (Fig. 6). In lateral view, tegumen protruding anteriorly; a small triangular plate at base of uncus; basal half of uncus pointed downwards at approximately 45°, distal half of uncus upturned and then slightly bent downwards, tapered into a sharp point; gnathos sickle-shaped, basal portion wide and elongated; saccus upturned, length about one third of the height of genitalia capsule. In dorsal view, basal half of tegumen semicircular; distal part of uncus widely bifid, tapered and bluntly pointed. In ventral view, left and right parts of gnathos separated. Distal half of valva bifid with a slender, sharply pointed dorsal branch curving downwards in lateral view and inwards in dorsal view, and a short blunt ventral branch. Aedeagus very robust; cornuti anchor shaped, extremely developed and sclerotized. Juxta V-shaped.

Figure 6. 

Male genitalia of Celaenorrhinus pyrrha from Chongqing [Dissection ID CQ125] A genital capsule, lateral view B genital capsule, dorsal view C genital capsule, ventral view D genital capsule, lateral view, valva and aedeagus removed E tegumen and gnathos, ventral view F right valva, inner surface G aedeagus, lateral view I aedeagus, with cornuti pulled out H aedeagus, dorsal view J juxta, posterior view.

Female genitalia (Fig. 7). Papillae anales trapezoidal, covered with short setae. Apophyses posteriors twice as long as papillae anales. Lamella postvaginalis, lamella antevaginalis and antrum merged together, with an elongated plate on each side of ostium. Ostium round, rather large. Ductus bursae short. Bursa copulatrix decorated with longitudinal striae, composed of two big bursae, dorsal side of first one coriaceous, with a longitudinal ridge and a number of transversal grooves.

Figure 7. 

Female genitalia of Celaenorrhinus pyrrha from Chongqing [Dissection ID CQ67] A ventral view B dorsal view a papillae anales b apophyses posteriors c lamella postvaginalis-lamella antevaginalis-antrum complex d ostium e ductus bursae f bursa copulatrix.

Discussion

According to our years of field surveys, and records in the literature (Evans 1949; Eliot 1959; Osada et al. 1999; Kimura et al. 2011; Ek-Amnury 2012; Monastyrskii and Devyatkin 2015), Celaenorrhinus pyrrha is a rather rare species throughout its distribution range (Fig. 8). In the present study, it is reported from two localities in China: Yingjiang in southwestern Yunnan, adjacent to northern Myanmar; and the Simian Mountain in southwestern Chongqing. The latter is isolated from the known distribution range of C. pyrrha (Evans 1949; Eliot 1959; Osada et al. 1999; Kimura et al. 2011; Ek-Amnury 2012; Monastyrskii and Devyatkin 2015) and the discovery of this species there is totally unexpected. In the present study, some minor external variations are recognized based upon examined specimens, for example: forewing length ranges from 22.4 cm to 26.0 cm; spaces C and Sc on the dorsal side of forewing may be unmarked, or with one or two small dots above the cell spot. However, we consider these as individual variations rather than intersubspecific differences because they exist in specimens from both Chongqing and Indochina. Genitalia characters of specimens from Chongqing, Yunnan, Thailand and Vietnam are compared for both sexes. According to our observations, the specimens from Chongqing cannot be distinguished by morphological characters, and thus do not represent a separate subspecies. Even so, the geographical isolation of Chongqing compared to other localities is worthy of attention, and C. pyrrha can possibly be expected from Guizhou, Guangxi and eastern Yunnan.

Figure 8. 

Distribution map of Celaenorrhinus pyrrha and C. munda. Triangle C. pyrrha a Yingjiang (Yunnan Province) b Simian Mountain (Chongqing) Circle C. munda Red C. munda munda Blue C. munda maculicornis Black C. munda joka c Cuona County (Tibet Autonomous Region) d Simla (Type locality of ssp. munda) e Khasi (Type locality of ssp. maculicornis).

Celaenorrhinus munda munda (Moore, 1884) (new record to China)

Fig. 4

Plesioneura munda Moore, 1884: 48, type locality: Simla, India.

Celaenorrhinus munda munda; Evans 1949: 100.

Material examined

China • 1?, Tibet, Cuona County, Lebugou, 19 June 2013, leg. Songyun Lang.

Description

Male genitalia (Fig. 9). In lateral view, tegumen protruding anteriorly; base of uncus with a semi-erect process; basal half of uncus quadrangular, distal half narrow, sloped, sharply pointed; gnathos sickle-shaped, distal end reaching tip of uncus; saccus pointing slightly downwards, length about half the height of genitalia capsule. In dorsal view, basal processes of uncus triangular, central part of uncus constricted, distal half of uncus bifid, forming a pair of horn-shaped blunt points. In ventral view, left and right parts of gnathos separated. Distal portion of valva bifid, divided into a wide ventral branch and a slender dorsal branch, disto-dorsal margin of the latter with a notch; both branches subequal in length and bent inwards. Aedeagus robust, distal half bent downwards; cornuti triangular and sharply pointed, well sclerotized. Juxta ring-shaped.

Figure 9. 

Male genitalia of Celaenorrhinus munda munda from Cuona, southern Tibet [Dissection ID Tib1] A genitalia capsule, lateral view, valva and aedeagus removed B tegumen and gnathos, dorsal view C tegumen and gnathos, ventral view D left valva, outer surface E left valva, inner surface F left valva, dorsal view G aedeagus, lateral view H aedeagus, dorsal view I aedeagus, ventral view J juxta, posterior view.

Discussion

Three subspecies have been described for Celaenorrhinus munda, of which C. munda joka Evans, 1949 is only known from the type locality, Tsekou, Yunnan, where the holotype was captured in 1898 as the only known exemplar of the species from China (Evans 1949).

Celaenorrhinus munda maculicornis Elwes & Edwards, 1897 is distributed from Sikkim, Assam to Myanmar (Evans 1949). The record of this subspecies from Thailand by Ek-Amnuay (2006: 752, pl. 345, H49b) was considered a misidentification of C. leucocera (Koller, 1844) (Ek-Amnuay et al. 2007: 14), but Ek-Amnuay (2012: 800, pl. 369, H47) included it again following Pinratana (1985: 28, 120, pl. 11, fig. 37), although Kimura et al. (2011: 34) had pointed out that Pinratana’s record is a misidentification. An earlier record of this subspecies from Thailand was listed by Godfrey (1930: 358) as C. maculicornis, but according to Kimura et al. (2011: 34) it is possibly a misidentification of C. putra (Moore). Devyatkin and Monastyrskii (1999) reported C. munda maculicornis from Vietnam for the first time based upon a female specimen, but in their later works, e.g., Monastyrskii and Devyatkin (2015), this name was not included, possibly because Dr. Devyatkin had realized that the specimen belongs to another species (Monastyrskii pers. comm. 2020). Therefore, we omit Vietnam from the distribution range of ssp. maculicornis (Fig. 8), since the identity of the female specimen needs further confirmation.

The nominate subspecies has been recorded from the northwestern Himalayas and Sikkim (Evans 1949). Ek-Amnuay (2006: 752, pl. 345, H49a) reported it from Thailand, but the photos of the specimens, which were provided by the second author of the present paper, actually represent C. dhanada dhanada (Inayoshi 2019). This mistake was corrected by Ek-Amnuay (2012: 800). Therefore, we omit Thailand from the distribution of C. munda in the present paper. Judging from the diagnosic characters provided by Evans (1949: 100), the specimen examined in this study belongs to C. munda munda. This discovery eastwardly expands the distribution range of the subspecies (Fig. 8).

Evans (1949) recorded both ssp. maculicornis and ssp. munda from Sikkim. Moreover, according to Devyatkin and Monastyrskii (1999), the two taxa are also found in Nepal, and the status of maculicornis remains controversial. Although differences in wing patterns of the two subspecies were clearly described by Evans (1949), the genitalia structures have not been illustrated and compared except for the simple hand drawing (Evans 1949: pl. 17, B.6. fig. 19). In future studies, comprehensive morphological and molecular analyses are needed to clarify the relationships of these taxa.

Acknowledgements

We express our sincere thanks to Dr. Songyun Lang (Chongqing), Dr. Hao Xu (Chongqing) and Mr. Kotaro Saito (Tokyo) for their various help. We are grateful to Dr. Alexander L. Monastyrskii (Hanoi), Dr. David J. Lohman (The City College of New York, USA) and the editor for their valuable comments on the manuscript. This study was funded by the National Natural Science Foundation of China (No. 41401067) and the Forest Resource Service Center of Simian Mountain, Chongqing.

References

  • de Nicéville CLA (1889) On new and little-known butterflies from the Indian region, with a revision of the genus Plesioneura of Felder and of Authors. Journal of the Bombay Natural History Society 4(3): 163–194.
  • Devyatkin AL, Monastyrskii AL (1999) Hesperiidae of Vietnam 5. An annotated list of the Hesperiidae of North and Central Vietnam (Lepidoptera, Hesperiidae). Atalanta 29(1/4): 151–184. [pl. XII]
  • Ek-Amnuay P (2006) Butterflies of Thailand. Fascinating Insects Vol. 2 (1st ed.). Amarin Printing and Publishing, Bangkok, 844 pp.
  • Ek-Amnuay P (2012) Butterflies of Thailand. 2nd revised ed. Amarin Printing and Publishing, Bangkok, 944 pp.
  • Ek-Amnuay P, Chiba H, Kimura Y, Inayoshi Y, Saito K, Seki Y, Uémura Y (2007) Corrigenda to “Butterflies of Thailand” (Ek-Amnuay, 2006). Yadoriga 213: 2–20.
  • Eliot JN (1959) New or little known butterflies from Malaya. Bulletin of the British Museum (Natural History) Entomology 7(8): 371–391. [pls 10]
  • Godfrey EJ (1930) A revised list of the butterflies of Siam, with notes on their geographical distribution. Journal of the Siam Society, Natural History Supplement 7(4): 203–397.
  • Hajibabaei M, Janzen DH, Burns JM, Hallwachs W, Hebert PDN (2006) DNA barcodes distinguish species of tropical Lepidoptera. Proceedings of the National Academy of Sciences 103(4): 968–971. https://doi.org/10.1073/pnas.0510466103
  • Kimura Y, Aoki T, Yamaguchi S, Uémura Y, Saito T (2011) The Butterflies of Thailand. Based on Yunosuke KIMURA Collection Vol. 1. Hesperiidae, Papilionidae, Pieridae. Mokuyosha, Tokyo, 220 pp.
  • Klots AB (1970) Lepidoptera. In: Tuxen SL (Ed.) Taxonomist’s Glossary of Genitalia in Insects (2nd ed. ). Munksgaard, Copenhagen, 115–130.
  • Kumar S, Stecher G, Tamura K (2016) MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Molecular Biology and Evolution 33(7): 1870–1874. https://doi.org/10.1093/molbev/msw054
  • Moore F (1884) Descriptions of some new Asiatic Lepidoptera; chiefly from specimens contained in the Indian Museum, Calcutta. Journal of the Asiatic Society of Bengal, Part II 53(1): 16–52.
  • Nakamura N, Wakahara H (2012) A revised checklist of the butterflies of the Lao P. D. R. (Insecta: Lepidoptera). Evolutionary Sciences 17: 19–85.
  • Osada S, Uémura Y, Uehara J (1999) An Illustrated Checklist of the Butterflies of Laos P D R. Mokuyo-sha, Tokyo, 240 pp.
  • Pinratana BA (1985) Butterflies in Thailand Vol. 5 Hesperiidae. The Viratham Press, Bangkok, 152 pp.
  • Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG (1997) The Clustal X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Research 25: 4876–4882. https://doi.org/10.1093/nar/25.24.4876
  • Wu CS, Hsu YF (2017) Butterflies of China. The Straits Publishing House, Fuzhou, 2036 pp.
  • Yuan F, Yuan XQ, Xue GX (2015) Fauna Sinica: Insecta. Vol. 55. Lepidoptera: Hesperiidae. Science Press, Beijing, 754 pp. [15 pls]

Supplementary material

Supplementary material 1 

Alignment of sequences

Guo-Xi Xue, Yutaka Inayoshi, Meng Li, Fu-Ming Zhang, Da-Kun Lai, Hai-Ying Tian

Data type: molecular data

This dataset is made available under the Open Database License (http://opendatacommons.org/licenses/odbl/1.0/). The Open Database License (ODbL) is a license agreement intended to allow users to freely share, modify, and use this Dataset while maintaining this same freedom for others, provided that the original source and author(s) are credited.
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