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Research Article
Taxonomic notes on the genus Yunohamella Yoshida, 2007 (Araneae, Theridiidae) from China, with two new species
expand article infoRui Zhong, Yang Zhong§, He Zhang|, Jie Liu, Changyong Liu#, Kuai Chen#, Changhao Hu¤
‡ Hubei University, Wuhan, China
§ Hubei University of Science and Technology, Xianning, China
| Xingtai University, Xingtai, China
¶ Hebei Province Sweet Potato Breeding and Application Technology Innovation Center, Xingtai, China
# Qizimeishan National Nature Reserve Administration, Xuan'en, China
¤ Hubei Broad Nature Technology Service Co., Ltd., Wuhan, China
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Abstract

Four Yunohamella species are reported from Hubei Province, China, including two new species: Y. gutenbergi R. Zhong, J. Liu & Hu, sp. nov. (♂) and Y. mohorovicici R. Zhong, J. Liu & Hu, sp. nov. (♂). Yunohamella jiugongensis (Liu & Zhong, 2023), comb. nov. is transferred from the genus Cryptachaea Archer, 1946, and Y. lyrica (Walckenaer, 1841) is newly recorded from Hubei Province and is considered as a senior synonym of Platnickina mneon (Bösenberg & Strand, 1906).

Key words

Biodiversity, comb-foot spiders, morphology, new combination, synonym, taxonomy

Introduction

Yunohamella Yoshida, 2007 is a small genus within the family Theridiidae Sundevall, 1833. To date, the genus contains eight described species (World Spider Catalog 2024), which are primarily distributed across the Eurasian continent, with four species recorded from China: Y. gibbosa Gao & Li, 2014, Y. lyrica (Walckenaer, 1841), Y. serpatusa (Guan & Zhu, 1993), and Y. subadulta (Bösenberg & Strand, 1906) (Zhu et al. 1993; Guan 2002; Yoshida 2007; Gao and Li 2014; Marusik and Logunov 2017; World Spider Catalog 2024). The first reported species of Yunohamella were originally classified in the genus Theridion Walckenaer, 1805. In 2001, Yoshida revised many species of Theridion. He described a new genus Takayus Yoshida, 2001 and designated two species groups in this genus, the takayensis group and the yunohamensis group, on the difference of the following characteristics: color of body, pattern on abdomen, scapus of epigynum, embolus and tegular apophysis of male palpus, and natural history. Yoshida (2007) later established the new genus Yunohamella based on the Takayus yunohamensis group earlier designated by him (Yoshida 2001) and transferred three species from Takayus to Yunohamella.

Yunohamella is placed in the subfamily Theridiinae Sundevall, 1833, and its phylogenetic placement shows it to be a sister group of the former Achaearanea Strand, 1929 sensu lato, which now is recognized as the genera Achaearanea, Campanicola Yoshida, 2015, Cryptachaea Archer, 1946, Nihonhimea Yoshida, 2016, and Parasteatoda Archer, 1946 (Liu et al. 2016).

The Qizimeishan National Nature Reserve, in southwestern Hubei, is characterized by a karst landscape. The reserve boasts rich forest vegetation and complex topography, providing ideal habitats that support the diversity and proliferation of the flora and fauna. Spiders of this nature reserve were surveyed from 2023 to 2024. In the current paper, we describe two new species of the genus Yunohamella from Qizimeishan National Nature Reserve and provide additional two taxonomic amendments.

Materials and methods

The specimens examined in this study are deposited in the Centre for Behavioral Ecology and Evolution (CBEE), College of Life Sciences, Hubei University in Wuhan and School of Nuclear Technology and Chemistry and Biology, Hubei University of Science and Technology (HUST) in Xianning. Specimens were examined using an Olympus SZX7 stereo microscope. Photographs were taken with a Leica M205 C stereo microscope, and final multifocal images were produced with Helicon Focus v. 7.7.0. The male palp was examined and photographed after dissection. The epigyne was examined after being dissected from the spider’s body. The epigyne was removed and treated in a warmed 0.1 mg/ml Protease K solution before study. All morphological measurements were calculated using a Leica M205 C stereo microscope. Eye diameters were taken at the widest point. Legs measurements are given as total length (femur, patella, tibia, metatarsus, tarsus). The terminologies used in figure legends follow Agnarsson (2004) and Agnarsson et al. (2007). All measurements were in millimeters (mm).

Abbreviations: ALE = anterior lateral eye; AME = anterior median eye; BH = basal haematodocha; C = conductor; CD = copulatory duct; CHd = cymbial hood; CO = copulatory opening; E = embolus; EB = embolic base; FD = fertilization duct; MA = median apophysis; PLE = posterior lateral eye; PME = posterior median eye; S = spermatheca; SD = sperm duct; ST = subtegulum; T = tegulum; TA = tegular apophysis; I, II, III, IV = legs I–IV.

Results

Taxonomy

Family Theridiidae Sundevall, 1833

Yunohamella Yoshida, 2007

Type species

Theridion yunohamense Bösenberg & Strand, 1906 (= Yunohamella yunohamensis) from Japan.

Diagnosis

Species of Yunohamella are similar to those of Takayus (compare Figs 2A–D, 4A–D, 5C–E, 6C, D, 7D–F, 8A, B, 9D–F; Gao and Li 2014: figs 107–109; Marusik and Logunov 2017: figs 37–39; Lee and Kim 2021: figs 3E–G, 4A,B with Zhu 1998: figs 80B–E, 83B–E, 93B–E, 94B–E, 108B–E, 114B–F, 115B–E, 116B–E, 117B–E, 118B–E, 119B–E, 120B–D, 125B, C) in having a large tegulum and a small median apophysis, a conductor conjugating with tegulum. However, Yunohamella can be distinguished from Takayus by the following: embolus thin; tegular apophysis distinct; and epigyne without a pointed scapus or with a blunt scapus (vs embolus broad, tegular apophysis invisible before expanded, epigyne with a pointed scapus in Takayus).

Species of Yunohamella can be distinguished from Theridion (compare Figs 2A–D, 4A–D, 5C–E, 6C, D, 7D–F, 8A, B, 9D–F; Gao and Li 2014: figs 107–109; Marusik and Logunov 2017: figs 37–39; Lee and Kim 2021: figs 3E–G, 4A, B with Zhu 1998: figs 73B–E, 76B–E, 85B–E, 88B–E, 89B–D, 90B–E, 91B, C, 97B–E, 98B–E, 106B–E, 109B–E, 110B–D 123B–E, 124B–E) by the following: embolus short and straight; tegulum large; conductor conjugating with tegulum; epigyne without depression (vs embolus long and circular; tegulum not large; conductor separated; epigyne with a distinct depression in Takayus) (Yoshida 2007).

Species of Yunohamella can be distinguished from Cryptachaea (compare Figs 2D, 4D, 8A, B; Levi 1957: fig. 323 with Levi 1955: fig. 82) in having a median apophysis separated from the embolus and the present tegular apophysis (vs median apophysis attached to the embolus and tegular apophysis absent in Cryptachaea).

Distribution

Asia, Europe, North America.

Yunohamella gutenbergi R. Zhong, J. Liu & Hu, sp. nov.

Figs 1, 2, 10

Type material

Holotype • male: China, Hubei Province: Enshi Tujia and Miao Autonomous Prefecture, Xuan’en County, Qizimeishan National Nature Reserve, Changtanhe Dong Autonomous Town, Shanyangxi; 30.08°N, 109.75°E; elev. 810 m; 3 July 2023; Changhao Hu & Mian Wei leg. (CBEE, QZMS01049).

Etymology

The species is named after the geophysicist “Beno Gutenberg” who found the “core-mantle discontinuity”, the boundary between the mantle and the core of Earth.

Diagnosis

Males of Y. gutenbergi R. Zhong, J. Liu & Hu, sp. nov. can be distinguished from all congeners in having a unique 2-shaped curved sperm duct on the tegulum and a filiform, curved embolus (Fig. 2A–C). Females are unknown.

Description

Male (holotype) measurements: total length 2.37. Carapace 1.10 long, 0.94 wide. Abdomen 1.29 long, 0.90 wide. Eyes: AME 0.10, ALE 0.08, PME 0.07, PLE 0.08, AMEAME 0.07, AMEALE 0.04, PMEPME 0.06, PMEPLE 0.08, AMEPME 0.10, ALEPLE 0.00. Measurements of legs [leg II missing]: I — (2.98, —, —, —, —), III 4.09 (1.38, 0.30, 0.86, 1.05, 0.50), IV 5.12 (1.79, 0.32, 1.35, 1.36, 0.30).

Carapace round, brown, and with a narrow, trapezoid, black mark between head region and median furrow; radial furrow black. Sternum shaped like an inverted triangle and brown. Chelicerae and legs orange. Abdomen oval; dorsally black, with a longitudinal mark composed of white and red spots; venter dark brown; anterior part of genital groove and anterior part of spinnerets black; lateral abdomen with several white spots. Spinnerets dark brown (Fig. 1A–C).

Figure 1. 

Yunohamella gutenbergi R. Zhong, J. Liu & Hu, sp. nov., male habitus. A dorsal view B ventral view C lateral view. Scale bars: 0.5 mm. (photos by Changhao Hu and Rui Zhong.)

Cymbium reniform. Cymbial hood longitudinal, almost ½ length of cymbium. Subtegulum bowl-shaped. Tegulum with a narrow prolateral part and a large retrolateral part; retrolateral part with a thin area that holds embolic base; sperm duct half surrounds thin area, and extends as 2-shaped, then straight down. Median apophysis lamellar. Tegular apophysis irregular. Length of median apophysis and tegular apophysis almost as long as width of bulb. Conductor sclerotized, with a triangular terminal apophysis. Embolus filiform and curved, with a lamellar base (Fig. 2A–D).

Figure 2. 

Yunohamella gutenbergi R. Zhong, J. Liu & Hu, sp. nov., left male palp. A prolateral view B ventral view C retrolateral view D expanded, ventral view. Scale bars: 0.2 mm. (Photos by Changhao Hu.)

Female. Unknown.

Distribution

Known only from the type locality (Fig. 10).

Yunohamella mohorovicici R. Zhong, J. Liu & Hu, sp. nov.

Figs 3, 4, 10

Type material

Holotype • male: China, Hubei Province: Enshi Tujia and Miao Autonomous Prefecture, Xuan’en County, Qizimeishan National Nature Reserve, Changtanhe Dong Autonomous Town, Qizimeishan mountain; 30.03°N, 109.73°E; elev. 1270 m; 6 July 2023; Changhao Hu & Mian Wei leg. (CBEE, QZMS04642).

Etymology

The species is named after the geophysicist “Andrija Mohorovičić” who found the “Moho discontinuity”, the boundary between the crust and the mantle of Earth.

Diagnosis

Males of Y. mohorovicici sp. nov. are similar to those of Y. jiugongensis (Liu & Zhong, 2023) comb. nov. (compare Fig. 4A–C with Fig. 5C–E) in having an n-shaped sperm duct on the tegulum and a thick, curved embolus, but Y. mohorovicici can be distinguished from Y. jiugongensis by the following: sharp tooth-like apophysis on tegulum absent; and terminal conductor rounded (vs apophysis on tegulum present and terminal conductor knife-shaped in Y. jiugongensis comb. nov.). Males of Y. mohorovicici sp. nov. are also similar to those of Y. palmgreni (Marusik & Tsellarius, 1986) (compare Fig. 4A–C with Marusik and Tsellarius 1986: figs 1, 2) in having an n-shaped sperm duct on the tegulum and a thick embolus, but Y. mohorovicici can be distinguished from Y. palmgreni by the following: conductor arising from the retrolateral part of the tegulum at the 2 o’clock position; and embolus curved (vs conductor arising from retrolateral part of the tegulum at the 12 o’clock position and embolus straight in Y. palmgreni). Females are unknown.

Description

Male (holotype), measurements: total length 1.77. Carapace 0.96 long, 0.77 wide. Abdomen 0.88 long, 0.65 wide. Eyes: AME 0.11, ALE 0.08, PME 0.07, PLE 0.07, AMEAME 0.06, AMEALE 0.03, PMEPME 0.05, PMEPLE 0.08, AMEPME 0.05, ALEPLE 0.01. Measurements of legs: I 6.80 (2.05, 0.37, 1.78, 1.92, 0.68), II 4.15 (1.29, 0.27, 0.99, 1.09, 0.51), III 2.70 (0.89, 0.19, 0.55, 0.67, 0.40), IV 3.66 (1.21, 0.25, 0.81, 0.95, 0.44). Leg formula: I-II-IV-III.

Carapace round, brown, with deep fovea and black radial furrow. Sternum shaped like an inverted triangle and brown. Labium brown. Chelicerae and endites orange. Legs yellow. Abdomen oval, with long hairs; dorsum black, with a longitudinal mark composed of white and red spots; venter brownish green; anterior part of spinnerets black; lateral abdomen with several white spots. Spinnerets brown (Fig. 3A–C).

Figure 3. 

Yunohamella mohorovicici R. Zhong, J. Liu & Hu, sp. nov., male habitus. A dorsal view B ventral view C lateral view. Scale bars: 0.5 mm. (Photos by Changhao Hu and Rui Zhong.)

Figure 4. 

Yunohamella mohorovicici R. Zhong, J. Liu & Hu, sp. nov., left male palp. A prolateral view B ventral view C retrolateral view D expanded, ventral view. Scale bars: 0.2 mm. (Photos by Changhao Hu.)

Figure 5. 

Yunohamella jiugongensis (Liu & Zhong, 2023) comb. nov., male. A habitus, dorsal view B habitus, ventral view C left palp, prolateral view D left palp, ventral view (arrow points to the sharp tooth-like apophysis on tegulum) E left palp, retrolateral view. Scale bars: 0.5 mm (A, B); 0.1 mm (C–E). (Photos by Yang Zhong.)

Cymbium reniform. Cymbial hood tilted at 60°, almost ¼ length of cymbium. Subtegulum bowl-shaped. Tegulum with a narrow prolateral part and a large retrolateral part; retrolateral part with a thin area that holds embolic base; sperm duct narrowly n-shaped. Median apophysis small, almost ½ length of tegular apophysis. Tegular apophysis large, knife-shaped; length of tegular apophysis almost as long as width of bulb. Conductor sclerotized, with smooth end. Embolus corn-like, thick, and curved, with a tooth-shaped base (Fig. 4A–D).

Female. Unknown.

Distribution

Known only from the type locality (Fig. 10).

Yunohamella jiugongensis (Liu & Zhong, 2023), comb. nov.

Figs 5, 6, 10

Cryptachaea jiugongensis Liu and Zhong in Liu et al. 2023: 98, figs 1A–F, 2A–E.

Type material

(examined). Holotype • male: China, Hubei Province: Xianning City, Jiugongshan National Nature Reserve, Yunzhonghu scenic spot; 29.39°N, 114.65°E; elev. 1230 m; 27 June 2021; Yang Zhong, Feng Lu, Han Dong & Jiangwei Zheng leg. (HUST, ZY2024001). Paratypes • 2 females, same data as holotype (HUST, ZY2024002).

Diagnosis

For males, see the above diagnosis under Y. mohorovicici sp. nov. Males of Y. jiugongensis comb. nov. are also similar to those of Y. palmgreni (compare Fig. 5C–E with Marusik and Tsellarius 1986: figs 1, 2) in having an n-shaped sperm duct on the tegulum and a thick embolus, but Y. jiugongensis comb. nov. can be distinguished from Y. palmgreni by the following: conductor arising from the retrolateral part of the tegulum at the 2 o’clock position; and embolus curved (vs conductor arising from the retrolateral part of tegulum at the 12 o’clock position and embolus straight in Y. palmgreni). Females of Y. jiugongensis comb. nov. are similar to those of Y. serpatusa (Guan & Zhu, 1993) (compare Fig. 6C, D with Esyunin and Efimik 1996: figs 3–5) in having a blunt scapus and the copulatory ducts almost as long as the diameter of the spermathecae, but Y. jiugongensis comb. nov. can be distinguished from Y. serpatusa by the parallel copulatory ducts (vs not parallel in Y. serpatusa). Females of Y. jiugongensis comb. nov. are also similar to those of Y. yunohamensis (Bösenberg & Strand, 1906) (compare Fig. 6C–D with Yoshida 2003: figs 233, 234) in having a scapus and copulatory ducts almost as long as the diameter of the spermathecae, but Y. jiugongensis comb. nov. can be distinguished from Y. yunohamensis by having an obtuse scapus and straight, parallel copulatory ducts (vs scapus with two rounded ends and copulatory ducts curved and not parallel in Y. yunohamensis).

Figure 6. 

Yunohamella jiugongensis (Liu & Zhong, 2023) comb. nov., female. A habitus, dorsal view B habitus, ventral view C epigyne, ventral view D vulva, dorsal view. Scale bars: 0.5 mm (A, B); 0.1 mm (C, D). (Photos by Yang Zhong.)

Redescription

Male, measurements: total length 1.77. Carapace 0.88 long, 0.76 wide. Abdomen 0.89 long, 0.77 wide. Eyes: AME 0.10, ALE 0.06, PME 0.08, PLE 0.07, AMEAME 0.06, AMEALE 0.03, PMEPME 0.06, PMEPLE 0.02, ALEPLE 0.02. Measurements of legs [legs I and IV missing]: II 3.36 (0.86, 0.30, 0.79, 0.93, 0.48), III 2.14 (0.67, 0.20, 0.38, 0.55, 0.34).

Carapace light brown, with black radial furrow. Sternum shaped like an inverted triangle and light brown. Chelicerae, labium, and endites brown. Legs yellow to orange. Abdomen black, with long hairs; dorsum with a grey longitudinal mark and some white spots; posterior dorsum with grey transverse marks; median band of ventral abdomen darker than the other bands. Spinnerets orange (Fig. 5A, B).

Subtegulum bowl-shaped. Tegulum with a narrow prolateral part and a large retrolateral part; retrolateral part with a thin area that holds embolic base; sperm duct narrowly n-shaped; tegulum with a sharp, tooth-like apophysis in ventral view. Median apophysis and tegular apophysis triangular in ventral view. Conductor sclerotized, with knife-shaped end. Embolus corn-like, thick, and curved (Fig. 5C–E).

Female, measurements: total length 3.53. Carapace 1.32 long, 1.16 wide. Abdomen 2.21 long, 1.81 wide. Eyes: AME 0.11, ALE 0.11, PME 0.09, PLE 0.12, AMEAME 0.07, AMEALE 0.06, PMEPME 0.07, PMEPLE 0.06, ALEPLE 0.02. Measurements of legs: I 7.90 (2.30, 0.42, 2.31, 2.09, 0.78), II 4.85 (1.45, 0.38, 1.22, 1.23, 0.57), III 3.08 (0.87, 0.26, 0.75, 0.66, 0.54), IV 5.56 (1.56, 0.53, 1.29, 1.51, 0.67). Leg formula: I-IV-II-III.

Carapace brown, with median band of carapace lighter than the rest of the carapace. Sternum brown. Abdomen light grey; dorsum with irregular black marks; posterior-lateral part of genital groove with black transverse bands, a rounded and two triangular black marks located around spinnerets. Other characters of habitus as for male (Fig. 6A, B).

Epigyne with a blunt scape; copulatory openings located medially at scape. Copulatory ducts straight and parallel, almost as long as diameter of spermathecae. Spermathecae spherical. Fertilization ducts thin, long, almost ½ diameter of spermathecae, and arising posteriorly from spermathecae (Fig. 6C, D).

Natural history

This species inhabits bushes.

Comments

The justification for the removal of Y. jiugongensis comb. nov. from Cryptachaea is supported by its distinct differences from diagnostic characteristics for Cryptachaea, particularly the median apophysis attached to the embolus and the absence of a tegular apophysis, a defining character for the genus Cryptachaea (Yoshida 2008; Rodrigues and Poeta 2015). In contrast, the male palp of Y. jiugongensis comb. nov. exhibits the presence of tegular apophysis. The species is placed into Yunohamella based on similarities of the palpal structures, specifically conductor conjugated with a large tegulum (Fig. 5C–E). This species also shares similarities in the epigynal structures with Yunohamella, specifically the presence of a blunt scapus (Fig. 6C, D), as well as similarities in the dark abdomen (Figs 5A, B, 6A, B). Consequently, we transfer C. jiugongensis from Cryptachaea to Yunohamella as a new combination.

Distribution

Known only from the type locality (Fig. 10).

Yunohamella lyrica (Walckenaer, 1841)

Figs 7, 8, 9, 10

Theridion lyricum Walckenaer, 1841: 288; Archer 1946: 43; Levi 1957: 89, figs 322–323, 329–331; Yoshida 1987: 13, figs 1, 2; Yoshida 1989: 318, fig. 4P–R; Chikuni 1989: 44, fig. 64; Kim and Kim 2001: 155, fig. 2A–I; Namkung 2002: 96, fig. 13.14a, b; Paquin and Dupérré 2003: 223, figs 2494–2496.

Theridion lyra Hentz, 1850: 279, pl. 9, fig. 21; Keyserling 1884: 50, pl. 2, fig. 28; Kaston 1948: 106, figs 132, 153, 154.

Theridion kentuckyense Keyserling, 1884: 78, pl. 4, fig. 47; Banks 1892: 30, pl. 5, fig. 43; Emerton 1909: 180, pl. 1, fig. 6.

Theridion mneon Bösenberg & Strand, 1906: 142, pl. 12, fig. 286.

Allotheridion lyricum: Archer 1950: 20.

Takayus lyricus: Yoshida 2001: 167; Namkung 2003: 98, fig. 13.14a, b; Yoshida 2003: 97, figs 239–242, 530.

Keijia mneon: Yoshida 2001: 172.

Yunohamella lyrica Yoshida 2007: 69; Yoshida 2009: 372, figs 149, 150; Lee and Kim 2021: 166, fig. 4A; Kim 2021: 172, fig. 75A–D.

Platnickina mneon: Koçak and Kemal 2008: 3; Ono 2011: 452; Dupérré 2023: 231, fig. 73A–C. Syn. nov.

Material examined

• 2 males, 4 females: China Hubei Province: Enshi Tujia and Miao Autonomous Prefecture, Xuan’en County, Qizimeishan National Nature Reserve, Chunmuying Town, Xiaoshui Cave; 30.02°N, 109.78°E; elev. 1777 m; 1 June 2024; Changhao Hu & Mian Wei leg. (CBEE, QZMS04713, QZMS04714, QZMS04751–QZMS04754). • 2 females: Enshi Tujia and Miao Autonomous Prefecture, Xuan’en County, Qizimeishan National Nature Reserve, Chunmuying Town, Xiaoshui Cave; 30.02°N, 109.78°E; elev. 1777 m; 12 July 2023; Changhao Hu & Mian Wei leg. (CBEE, QZMS02405, QZMS02406). • 1 female: Enshi Tujia and Miao Autonomous Prefecture, Xuan’en County, Qizimeishan National Nature Reserve, Chunmuying Town, Shaiping Village; 29.96°N, 109.76°E; elev. 1822 m; 31 July 2023; Changhao Hu & Mian Wei leg. (CBEE, QZMS01160).

Diagnosis

For males see the diagnosis under Y. varietas by Lee and Kim (2021). Males of Y. lyrica are also similar to those of Y. subadulta (compare Fig. 7D–F with Kim 2021: fig. 77E–G) in having a sharp terminal conductor and a sperm duct curving four times, but Y. lyrica can be distinguished from Y. subadulta in having the conductor extend beyond the cymbium (vs. conductor not exceeding the cymbium in Y. palmgreni). Females of Y. lyrica are similar to those of Y. takasukai Yoshida, 2012 (compare Fig. 9D–F with Yoshida 2012: figs 4, 5) in having a pair of projections on the anterlateral epigynal plate, but Y. lyrica can be distinguished from Y. takasukai by having oval, laminar projections on the anterlateral epigynal plate and long, curved copulatory ducts (vs nipple-like projections and copulatory ducts short in Y. takasukai).

Figure 7. 

Yunohamella lyrica (Walckenaer, 1841), male. A habitus, dorsal view B habitus, ventral view C habitus, lateral view D left palp, prolateral view E left palp, ventral view F left palp, retrolateral view. Scale bars: 0.5 mm (A–C); 0.2 mm (D–F). (Photos by Changhao Hu and Rui Zhong.)

Redescription

Male, measurements: total length 2.11. Carapace 1.16 long, 0.88 wide. Abdomen 1.10 long, 0.91 wide. Eyes: AME 0.10, ALE 0.08, PME 0.08, PLE 0.08, AMEAME 0.10, AMEALE 0.04, PMEPME 0.07, PMEPLE 0.09, AMEPME 0.09, ALEPLE 0.00. Measurements of legs: I 7.48 (2.27, 0.43, 1.94, 2.10, 0.74), II 4.29 (1.38, 0.30, 0.98, 1.17, 0.46), III 2.71 (1.00, 0.19, 0.52, 0.60, 0.40), IV 3.87 (1.31, 0.26, 0.88, 0.95, 0.47). Leg formula: I-II-IV-III.

Carapace brownish green, with deep fovea and black radial furrow. Sternum shaped like an inverted triangle and dark brown. Chelicerae orange. Labium and endites dark brown. Legs yellow. Abdomen with long hairs; dorsum black, with a longitudinal mark composed of yellow base and white spots; venter yellow; anterior part of spinnerets black. Spinnerets brown (Fig. 7A–C).

Cymbium oval. Cymbial hood tilted at 30°, almost 1/8 length of cymbium. Subtegulum bowl-shaped. Tegulum with a narrow prolateral part and a large retrolateral part; sperm duct curving four times. Median apophysis and tegular apophysis almost as long as the width of bulb. Conductor sclerotized, with a sharp end. Embolus straight, with a rounded base (Figs 7D–F, 8A, B).

Figure 8. 

Yunohamella lyrica (Walckenaer, 1841), expanded left male palp. A prolateral view B ventral view. Scale bars: 0.2 mm. (Photos by Changhao Hu.)

Female, measurements: total length 2.49. Carapace 0.91 long, 0.74 wide. Abdomen 1.40 long, 1.31 wide. Eyes: AME 0.09, ALE 0.07, PME 0.09, PLE 0.09, AMEAME 0.04, AMEALE 0.02, PMEPME 0.08, PMEPLE 0.07, AMEPME 0.05, ALEPLE 0.00. Measurements of legs: I 5.57 (1.73, 0.32, 1.47, 1.43, 0.62), II 3.76 (1.24, 0.33, 0.83, 0.86, 0.50), III 2.71 (0.94, 0.25, 0.51, 0.61, 0.40), IV 3.84 (1.30, 0.34, 0.84, 0.91, 0.45). Leg formula: I-IV-II-III.

Carapace dark brown. Legs yellow to orange. Abdomen black; dorsum with a longitudinal mark composed of white, red, and yellow spots; posterior part of dorsum with three inverted V-shaped marks composed of yellow spots; median band of venter black, the rest yellow; posterior part of genital groove with several white spots, posterior-lateral part of genital groove with black transverse bands. Other characters of habitus as for male (Fig. 9A–C).

Epigyne with an oval atrium, two oval sclerotized plates overhanging anterolateral epigynal plate, copulatory openings located laterally on sclerotized plates. Copulatory ducts curved into a C-shape. Spermathecae spherical. Fertilization ducts arising posteriorly from spermathecae (Fig. 9D–F).

Figure 9. 

Yunohamella lyrica (Walckenaer, 1841), female. A habitus, dorsal view B habitus, ventral view C habitus, lateral view D uncleared epigyne, ventral view E uncleared epigyne, ventral view F vulva, dorsal view. Scale bars: 0.5 mm (A–C); 0.1 mm (D–F). (Photos by Changhao Hu.)

Natural history

This is one of the most widespread Yunohamella species. This species is found on bushes, forests, and fences, as well as inside houses (Kaston 1948; Levi 1957; Gao and Li 2014; Kim et al. 2016; Lee and Kim 2021).

Comments

Platnickina mneon was first described by Bösenberg and Strand (1906) based on a female specimen collected in Saga, Japan. To date, males of P. mneon remain unknown. Dupérré (2023) provided diagnostic characters and illustrations of P. mneon after examining the female holotype and noted that this species does not conform to the characteristics of the genus Platnickina Koçak & Kemal, 2008 (e.g. copulatory openings located on sclerotized plates in P. mneon vs inside the circular depression of the epigyne in Platnickina spp.) and that it likely belongs to another genus. The holotype of P. mneon exhibits all the diagnostic features of Y. lyrica as provided by Levi (1957), including the two sclerotized plates, copulatory openings located on the sclerotized plates, and oval spermathecae (compare Figs 7D–F, 9D–F with Dupérré 2023: fig. 73B, C and with Levi 1957: figs 329, 330). Although the types of Y. lyrica and P. mneon were unavailable for examination, our comparison based on specimens collected in Hubei Province, China and the illustrations and descriptions provided by Levi (1957) and Dupérré (2023) allows us to consider P. mneon as a junior synonym of Y. lyrica.

Figure 10. 

The collection locality of Yunohamella spp. from Hubei Province, China. Black circle represents Y. gutenbergi R. Zhong, J. Liu & Hu, sp. nov.; green circle represents Y. mohorovicici R. Zhong, J. Liu & Hu, sp. nov.; red circle represents Y. jiugongensis (Liu & Zhong, 2023) comb. nov.; orange circles represent Y. lyrica (Walckenaer, 1841).

Distribution

China (Hubei Province, new Province record; Yunnan Province), Japan, Korea, North America.

Acknowledgements

We thank Mian Wei (CBEE) for helping specimens’ collection and identification. This manuscript benefitted greatly from the subject editor Francesco Ballarin, the copy editor Robert Forsyth, and the reviewers Ingi Agnarsson and Yejie Lin.

Additional information

Conflict of interest

The authors have declared that no competing interests exist.

Ethical statement

No ethical statement was reported.

Funding

This research was funded by the National Natural Sciences Foundation of China (NSFC-32270495/32300378/32400360), the Science & Technology Fundamental Resources Investigation Program of China (2023FY100200), the Foundation of Hubei Key Laboratory of Regional Development and Environmental Response (2022(B)004), and the China Postdoctoral Science Foundation (2023M731035).

Author contributions

Writing – original draft: RZ, CH. Writing – review and editing: RZ, YZ, JL, HZ, CL, KC, CH.

Author ORCIDs

Rui Zhong https://orcid.org/0000-0001-5910-7302

Yang Zhong https://orcid.org/0000-0002-0517-4582

He Zhang https://orcid.org/0000-0002-1478-9837

Jie Liu https://orcid.org/0000-0001-7744-9744

Changhao Hu https://orcid.org/0009-0007-5591-3121

Data availability

All of the data that support the findings of this study are available in the main text.

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