Research Article |
Corresponding author: Zhiyuan Yao ( yaozy@synu.edu.cn ) Academic editor: Gergin Blagoev
© 2020 Xiang Wang, Shumaila Shaheen, Qiaoqiao He, Zhiyuan Yao.
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:
Wang X, Shaheen S, He Q, Yao Z (2020) Notes on two closely related spider species of the Pholcus phungiformes species group (Araneae, Pholcidae) from Beijing, China. ZooKeys 965: 1-16. https://doi.org/10.3897/zookeys.965.56199
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The Pholcus phungiformes species group is highly diverse and currently contains 53 species. In this study, Pholcus tongyaoi Wang & Yao, sp. nov. (male, female) from Huairou District, Beijing, China is described while similar congener Pholcus lexuancanhi Yao, Pham & Li, 2012 from neighboring Haidian District (type locality) is redescribed; the female of P. lexuancanhi is described for the first time. In addition, the DNA barcode COI for the two species was obtained to estimate p-distance.
daddy-long-leg spider, DNA barcode, morphology, Pholcinae, taxonomy
The spider family Pholcidae C.L. Koch, 1850 contains 94 genera and 1768 species (
In this study, we describe one new species based on males and females from Huairou District, Beijing, China assigned to the P. phungiformes species group and redescribe its similar species Pholcus lexuancanhi Yao, Pham & Li, 2012 from a neighboring locality. The female of P. lexuancanhi is reported for the first time and the DNA barcode COI for the two species was obtained to estimate p-distance.
Specimens were examined and measured with a Leica M205 C stereomicroscope. Left male pedipalps were illustrated. External female genitalia were photographed before dissection. Vulvae were previously treated in a 10% warm solution of potassium hydroxide (KOH) to dissolve soft tissues before illustration. Images were captured with a Canon EOS 750D wide zoom digital camera (24.2 megapixels) mounted on the stereomicroscope mentioned above, and assembled using Helicon Focus 3.10.3 image stacking software (
Terminology and taxonomic descriptions follow
ALE anterior lateral eye,
AME anterior median eye,
PME posterior median eye,
L/d length/diameter.
DNA barcode was obtained for estimation of p-distance between P. tongyaoi sp. nov. and P. lexuancanhi. A partial fragment of the mitochondrial cytochrome oxidase subunit I (COI) gene was amplified and sequenced, using the following primers: forward: LCO1490-oono (5’-CWACAAAYCATARRGATATTGG-3’) and reverse: C1-N-2776 (5’-GGATAATCAGAATANCGNCGAGG-3’). DNA sample is preserved in TE buffer and stored at -20 °C. The sequences are deposited in GenBank. COI p-distance is computed with MEGA 5 (
Subfamily Pholcinae C.L. Koch, 1850
Aranea phalangioides Fuesslin, 1775.
See
The ‘appendix’ in the original figures of four species apparently arises from the uncus: P. papilionis Peng & Zhang, 2011, P. chiakensis Seo, 2014, P. gajiensis Seo, 2014, and P. palgongensis Seo, 2014. We consider this a divided ‘pseudo-appendix’ and assign them to the P. phungiformes species group. Moreover, although the species P. xianrendong Liu & Tong, 2015 does not possess a prolatero-ventral projection on the male pedipalpal tibia, the bulb without appendix, the locality of this species is within the range of the P. phungiformes species group. Therefore, we tentatively assigned P. xianrendong to this species group. In total, this species group now contains 59 species. Of these, one species is newly described below.
Holotype : male (SYNU-Ar00016), Pool and Valley Natural Park (40°32.600'N, 116°40.687'E, elevation 574 m), Huairou District, Beijing, China, 26 April 2019, T Jiang leg. Paratypes: 2 males (SYNU-Ar00017, Ar00018, GenBank number in SYNU-Ar00017: MT843113), same data as holotype; 2 females (SYNU-Ar00019, Ar00020), same data as holotype but 23 April 2019.
The specific name is a patronym in honor of the collector Tongyao Jiang (
The species resembles P. lexuancanhi Yao, Pham & Li, 2012 (Figs
Pholcus tongyaoi sp. nov., holotype (A, B, D) and paratype (C) males A, B pedipalp (A prolateral view, arrow indicates ventral membranous process B retrolateral view, arrow indicates ventral sclerite) C, D distal part of procursus (C prolateral view, arrow 1 indicates prolateral membranous lamella, arrow 2 indicates spine-shaped prolateral apophysis, arrow 3 indicates ventral membranous process D dorsal view, arrow indicates dorsal spine). Abbreviations: b = bulb, e = embolus, pr = procursus, u = uncus. Scale bars: 0.20 (A, B), 0.10 (C, D).
Male (holotype, SYNU-Ar00016): Total length 4.75 (4.93 with clypeus), carapace 1.56 long, 1.75 wide, opisthosoma 3.19 long, 1.34 wide. Leg I: – (11.62 + 0.75 + – + – + –), leg II: 30.89 (8.50 + 0.55 + 7.84 + 12.75 + 1.25), leg III: 20.62 (6.40 + 0.60 + 5.12 + 7.60 + 0.90), leg IV: 28.58 (8.40 + 0.62 + 7.12 + 11.12 + 1.32). Distance PME-PME 0.20, diameter PME 0.12, distance PME-ALE 0.05, distance AME-AME 0.02, diameter AME 0.08. Sternum wider than long (1.04/0.96). Habitus as in Fig.
Female (paratype, SYNU-Ar00019): Similar to male, habitus as in Fig.
Pholcus tongyaoi sp. nov., holotype male (C–F) and paratype female (A, B, G, H) A external female genitalia, ventral view B vulva, dorsal view C bulbal apophyses, prolateral view, arrow indicates ‘pseudo-appendix’ D chelicerae, frontal view E–H habitus (E, G dorsal view F lateral view H ventral view). Abbreviations: da = distal apophysis, e = embolus, fa = frontal apophysis, pa = proximo-lateral apophysis, pp = pore plate, u = uncus. Scale bars: 0.20 (A–D), 1.00 (E–H).
Ventral membranous process on procursus nearly crescent-shaped (arrowed 3 in Fig.
China (Beijing, type locality; Fig.
The species was found in an old house and on rock walls.
Pholcus lexuancanhi
2 males (
See diagnosis for P. tongyaoi sp. nov.
Male (
Pholcus lexuancanhi Yao, Pham & Li, 2012, male A, B pedipalp (A prolateral view B retrolateral view, arrow indicates ventral sclerite) C, D distal part of procursus (C prolateral view, arrows 1 and 2 indicate prolateral and dorsal membranous lamella, respectively, arrow 3 indicates spine-shaped prolateral apophysis D dorsal view, arrow indicates dorsal spine). Abbreviations: b = bulb, e = embolus, pr = procursus, u = uncus. Scale bars: 0.20 (A, B), 0.05 (C, D).
Female (
Pholcus lexuancanhi Yao, Pham & Li, 2012, male (C–F) and female (A, B, G, H) A external female genitalia, ventral view B vulva, dorsal view, arrow indicates median sclerite of anterior arch C bulbal apophyses, prolateral view, arrow indicates ‘pseudo-appendix’ D chelicerae, frontal view E–H habitus (E, G dorsal view F lateral view H ventral view). Abbreviations: da = distal apophysis, e = embolus, pa = proximo-lateral apophysis, pp = pore plate, u = uncus. Scale bars: 0.20 (A–D), 1.00 (E–H).
Tibia I in another male (
China (Beijing, type locality; Fig.
The species was found on rock walls.
The P. phungiformes species group is highly diverse and currently contains 59 species including one new species in this study. These species are mainly distributed in three large mountain ranges (see the checklist below): the Mountain Taihang from southern North China (22 spp.), the Mountain Changbai (also called Mountain Paekdu in North Korea) from the border between northeastern China and North Korea (15 spp., of which P. phungiformes also occurs further east), and the Mountain Taebaek from Korean Peninsula (22 spp.) (
A checklist of the P. phungiformes species group from three large mountain ranges is provided (for the complete list of references, see
The Mountain Taihang:
1. Pholcus alloctospilus Zhu & Gong, 1991
2. Pholcus auricularis Zhang, Zhang & Liu, 2016
3. Pholcus babao Tong & Li, 2010
4. Pholcus beijingensis Zhu & Song, 1999
5. Pholcus brevis Yao & Li, 2012
6. Pholcus chicheng Tong & Li, 2010
7. Pholcus clavimaculatus Zhu & Song, 1999
8. Pholcus curvus Zhang, Zhang & Liu, 2016
9. Pholcus datan Tong & Li, 2010
10. Pholcus exilis Tong & Li, 2010
11. Pholcus jinniu Tong & Li, 2010
12. Pholcus lexuancanhi Yao, Pham & Li, 2012
13. Pholcus luya Peng & Zhang, 2013
14. Pholcus papilionis Peng & Zhang, 2011
15. Pholcus papillatus Zhang, Zhang & Liu, 2016
16. Pholcus pennatus Zhang, Zhu & Song, 2005
17. Pholcus suizhongicus Zhu & Song, 1999
18. Pholcus tongyaoi sp. nov.
19. Pholcus triangulatus Zhang & Zhang, 2000
20. Pholcus wangxidong Zhang & Zhu, 2009
21. Pholcus wuling Tong & Li, 2010
22. Pholcus zhuolu Zhang & Zhu, 2009
The Mountain Changbai:
1. Pholcus decorus Yao & Li, 2012
2. Pholcus fengcheng Zhang & Zhu, 2009
3. Pholcus foliaceus Peng & Zhang, 2013
4. Pholcus gaoi Song & Ren, 1994
5. Pholcus hamatus Tong & Ji, 2010
6. Pholcus jiuwei Tong & Ji, 2010
7. Pholcus lingulatus Gao, Gao & Zhu, 2002
8. Pholcus ningan Yao & Li, 2018
9. Pholcus phoenixus Zhang & Zhu, 2009
10. Pholcus phungiformes Oliger, 1983
11. Pholcus sublingulatus Zhang & Zhu, 2009
12. Pholcus tongi Yao & Li, 2012
13. Pholcus wangi Yao & Li, 2012
14. Pholcus wangtian Tong & Ji, 2010
15. Pholcus xianrendong Liu & Tong, 2015
The Mountain Taebaek:
1. Pholcus acutulus Paik, 1978
2. Pholcus cheongogensis Kim & Ye, 2015
3. Pholcus chiakensis Seo, 2014
4. Pholcus crassus Paik, 1978
5. Pholcus extumidus Paik, 1978
6. Pholcus gajiensis Seo, 2014
7. Pholcus gosuensis Kim & Lee, 2004
8. Pholcus joreongensis Seo, 2004
9. Pholcus juwangensis Seo, 2014
10. Pholcus kwanaksanensis Namkung & Kim, 1990
11. Pholcus kwangkyosanensis Kim & Park, 2009
12. Pholcus montanus Paik, 1978
13. Pholcus nodong Huber, 2011
14. Pholcus okgye Huber, 2011
15. Pholcus palgongensis Seo, 2014
16. Pholcus parkyeonensis Kim & Yoo, 2009
17. Pholcus pojeonensis Kim & Yoo, 2008
18. Pholcus simbok Huber, 2011
19. Pholcus socheunensis Paik, 1978
20. Pholcus sokkrisanensis Paik, 1978
21. Pholcus woongil Huber, 2011
22. Pholcus yeongwol Huber, 2011
The manuscript benefited greatly from comments by Gergin Blagoev, Marc Milne, and John TD Caleb. We are grateful to Tongyao Jiang for providing the ecological photographs and specimens. Abid Ali kindly checked the English. This study was supported by the National Natural Science Foundation of China (NSFC-31872193) and the Liaoning Revitalization Talents Program (XLYC1907150). Part of the laboratory work was supported by the Research Fund for the Doctoral Program of Shenyang Normal University (BS201841) and the Shenyang Youth Science and Technology Project (RC200183).