Biodiversity Data Journal :
Taxonomy & Inventories
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Corresponding author: Yang Zhong (hubeispider@aliyun.com)
Academic editor: Yanfeng Tong
Received: 25 Jun 2024 | Accepted: 19 Jul 2024 | Published: 02 Aug 2024
© 2024 Lelei Wen, Changchun Li, Yang Zhong
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:
Wen L, Li C, Zhong Y (2024) One new species of Pseudopoda Jäger, 2000 from Shennongjia, Central China (Araneae, Sparassidae). Biodiversity Data Journal 12: e130445. https://doi.org/10.3897/BDJ.12.e130445
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Pseudopoda Jäger, 2000 is currently the largest genus in the family Sparassidae Bertkau, 1872, comprising 255 species. Of these, 154 species have been recorded in China, representing 60.4% of the global species.
In October 2023, a spider survey was conducted in Shennongjia National Nature Reserve, Hubei Province, China. After examination and morphological comparison, one new species of the genus Pseudopoda was identified and is described here.
In this paper, a new species of Pseudopoda collected in Hubei Province, China, is proposed and named Pseudopoda guanmenshan sp. nov. A detailed description, diagnosis, photographs and distribution map of the new species are provided.
huntsman spiders, morphology, new species, taxonomy
The genus of Pseudopoda occurs in areas of South Asia (49 species in Nepal, India, Bhutan and Pakistan), East Asia (159 species in China and Japan) and Southeast Asia (53 species in Myanmar, Thailand, Laos and Vietnam) (
To date, there are 154 species distributed in China and only four of these species have been described in Hubei Province (
Shennongjia, located in the transition zone between the second and third terraces in China's Hubei Province, is endowed with extremely rich resources and is one of the most important ecological functional areas and ecological vulnerability zones in the world (
The specimens were collected on leaves at night with bare hands. The type specimens are deposited in the School of Nuclear Technology and Chemistry & Biology, Hubei University of Science and Technology, Xianning, China. Specimens were preserved in 95% alcohol and examined using an Olympus SZX7 stereomicroscope. Left male palps were examined and photographed after dissection. Epigynes were removed and cleared in proteinase K at 56°C to dissolve non-chitinous tissues. The vulva was imaged after being embedded in Arabic gum. All photographs were captured with a KUY NICE industrial digital camera (20.0 megapixels), mounted on an Olympus CX43 dissecting microscope and assembled using Helicon Focus 3.10.3 image stacking software. All measurements were obtained using an Olympus SZX7 stereomicroscope and are given in millimetres. Eye diameters were measured at the widest part. The total body length does not include the chelicerae or spinnerets. Leg formula, spination and measurements of eye, palp and legs follow
The abbreviations used in the text are: ALE = anterior lateral eye; AME = anterior median eye; AW = anterior width of carapace; BB = basal bulge of dorsal RTA; C = conductor; CO = copulatory opening; CH = clypeus height; dRTA = dorsal branch of RTA; E = embolus; EB = epigynal bulges; EP= embolic projection; F = finger-like tip of dorsal RTA; Fe = femur; FD = fertilisation duct; FW = first winding; LL = lateral lobes; Mt = metatarsus; MS = membranous sac; OL = opisthosoma length; OW = opisthosoma width; Pa = patella; PI = posterior incision of LL; PL = prosoma length; PLE = posterior lateral eyes; PME = posterior median eyes; PW = prosoma width; RTA = retrolateral tibial apophysis; S = spermatheca; Sp = spermophore; St = subtegulum; T = tegulum; Ti = tibia; I, II, III, IV = legs I to IV; vRTA = ventral branch of RTA.
Male. PL 5.0, PW 4.6, AW 2.7, OL 6.6, OW 4.7. Eyes: AME 0.24, ALE 0.34, PME 0.26, PLE 0.38, AME–AME 0.18, AME–ALE 0.07, PME–PME 0.24, PME–PLE 0.18, AME–PME 0.29, ALE–PLE 0.17, CH–AME 0.35, CH–ALE 0.47. Setation: Palp: 131, 101, 2101; Fe: I–III 323, IV 321; Pa: I–IV 101; Ti: I–II 2026, III–IV 2126; Mt: I–II 1014, III 2026, IV 3036. Measurements of palp and legs: Palp 6.4 (2.1, 0.7, 1.0, –, 2.6), I 19.3 (5.5, 1.3, 5.6, 5.1, 1.8), II 20.5 (5.9, 1.3, 6.1, 5.4, 1.8), III 15.4 (4.6, 1.1, 4.5, 3.7, 1.5), IV 16.9 (5.0, 1.0, 4.5, 4.6, 1.8). Leg formula: II-I-IV-III. The carapace is yellowish-brown dorsally, with black patches, shallow fovea and radial furrows. Chelicerae are pale reddish-brown. The sternum is yellow, with a few random black spots. Endites and labium are yellowish-brown. Legs are yellow, with brown dots randomly distributed and covered by short spines and setae. The dorsal opisthosoma is yellowish-brown with two pairs of dark muscle sigilla and a white transversal band in the posterior half. The ventral opisthosoma is uniformly yellowish-brown with some black patches (Fig.
Pseudopoda guanmenshan sp. nov., habitus (A–D), cheliceral dentition (E, F), live specimens (G) and schematic course of internal duct system (H). A, B, E holotype male (HUST-SPA-24-001); C, D, F paratype female (HUST-SPA-24-002). A, C, G dorsal view; B, D, E , F ventral view. Scale bar: A–D 1 mm; E, F 0.5 mm.
Cymbium approximately 2.5 times the length of the tibia. Spermophore running submarginally and retrolaterally in tegulum. Conductor arising from tegulum at 12:00 o’clock position, covering the tip of embolus. Basal part of embolus broad, almost covering subtegulum, while the distal part tapers gradually and becomes trapezoidal at distal end. Embolic projection emerging at the middle margin of embolus as a pointed hump. Anterior margin of vRTA almost straight in ventral view (Fig.
Pseudopoda guanmenshan sp. nov., male holotype (HUST-SPA-24-001), left palp (A–C), A prolateral view; B ventral view; C retrolateral view. Abbreviations: BB = basal bulge of dorsal RTA; C = conductor; E = embolus; EP = embolic projection; F = finger-like tip of dorsal RTA; Sp = spermophore; St = subtegulum; T = tegulum; vRTA = ventral branch of RTA. Scale bar: 0.5 mm.
Female. PL 5.2, PW 4.5, AW 2.7, OL 5.4, OW 3.5. Eyes: AME 0.23, ALE 0.30, PME 0.26, PLE 0.32, AME–AME 0.20, AME–ALE 0.11, PME–PME 0.33, PME–PLE 0.26, AME–PME 0.25, ALE–PLE 0.26, CH AME 0.35, CH ALE 0.37. Setation: Palp: 131, 101, 2121, 1014; Fe: I–III 323, IV 321; Pa: I–IV 101; Ti: I–IV 2126; Mt: I–II 2024, III–IV 3036. Measurements of palp and legs: Palp 6.1 (2.0, 0.5, 1.3, –, 2.3), I 18.7 (5.4, 1.3, 5.4, 4.9, 1.7), II 19.4 (5.7, 1.3, 5.8, 5.0, 1.6), III 15.1 (4.8, 1.1, 4.3, 3.7, 1.2), IV 16.1 (5.0, 1.1, 4.1, 4.5, 1.4). Leg formula: II-I-IV-III. Chelicerae with three promarginal and four retromarginal teeth and with ~ 32 denticles (Fig.
Epigynal field clearly wider than long; median margin of lateral lobes parallel and almost straight; posterior incision of lateral lobes and epigynal bulges distinct. Copulatory opening located at middle part of epigyne. In dorsal view, space between fertilisation ducts and first winding smaller than width of first winding, posterior end of first winding of internal duct system freely visible. Membranous sac between fertilisation ducts almost trapezoidal (Fig.
Pseudopoda guanmenshan sp. nov., female paratype (HUST-SPA-24-002), epigyne (A, B), vulva (C). A ventral view; B ventral view, macerated and embedded in Arabic gum; C dorsal view, macerated and embedded in Arabic gum. Abbreviations: CO = copulatory opening; EB = epigynal bulges; FD = fertilisation duct; FW = first winding; LL = lateral lobes; MS = membranous sac; PI = posterior incision of LL; S = spermatheca. Scale bar: 0.3 mm.
Colouration as in males, opisthosoma brown dorsally (Fig.
Males of Pseudopoda guanmenshan sp. nov. are similar to those of P. tji Jäger, 2015 (
The species name is derived from the name of the type locality; noun in apposition.
We have presented the copulatory behaviour diagram for this newly-identified species within its native habitat (Fig.
We are especially grateful to Prof. Yanfeng Tong (Shenyang Normal University), the subject editor of this manuscript. This study was financially supported by the National Natural Sciences Foundation of China (32000303), the Natural Sciences Foundation of Hubei Province (2024AFC060), the Scientific Research Project of Education Department of Hubei Province (Q20222806), the Natural Sciences Foundation of Xianning City (2022ZRKX063) and the Hubei Province Key Laboratory of Conservation Biology for Shennongjia Golden Monkey Foundation (No. SNJKL2021003).