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Research Article
Notes on two species of Massuria Thorell, 1887 (Arachnida, Araneae, Thomisidae) from China with description of a new species
expand article infoCong-zheng Li, Yan-bin Yao§, Yong-hong Xiao, Xiang Xu|, Ke-ke Liu
‡ Jinggangshan University, Ji’an, China
§ Jinshan College of Fujian Agriculture and Forestry University, Fuzhou, China
| Hunan Normal University, Changsha, China
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Abstract

Two species assigned to Massuria Thorell, 1887 are reviewed. The female of Massuria bandian Tang & Li, 2010 is described for the first time from Jianfengling National Natural Reserve, Hainan Province, China. The species Diaea simplex Xu, Han & Li, 2008 is described as a synonym of Massuria bellula Xu, Han & Li, 2008 based on female and male specimens from Guangdong Province, China. Massuria min sp. nov. described as a new species (female, Fujian Province, China). Detailed illustrations and a distribution map are provided for these three species of Massuria.

Key words

Crab spiders, new combination, single sex, supplement, taxonomy

Introduction

Based on the combination of morphological and molecular identification methods, approximately 750 new spider species have been reported from China in the last three years (Li 2020; Yao et al. 2021; Liu et al. 2022a, b; Lu et al. 2022). Many new taxa have been discovered, which means that more taxa need to be revised, re-assigned, or supplemented with appropriate identification methods; one such family is the crab spiders Thomisidae Sundevall, 1833. Although there are several recent publications dealing with descriptions of previously unknown sexes of Chinese crab spiders, there are still many species requiring study (Meng et al. 2019; Wang et al. 2020; Lin et al. 2022; Liu et al. 2022b; Zhong et al. 2022).

Massuria was established by Thorell (1887) based on a single female specimen described as M. angulata Thorell, 1887 from Myanmar. Lehtinen (2004) transferred two Pistius species recorded from India to this genus, including M. roonwali (Basu, 1964) and M. sreepanchamii (Tikader, 1962), the latter including the first description of males in this genus. The generic characters were better understood after Ono (2002) and Tang and Li (2010b) described three new species, M. bandian Tang & Li, 2010, M. ovalis Tang & Li, 2010 and M. watari Ono, 2002.

Currently, there are nine valid species of Massuria recorded from Asia (World Spider Catalog 2023). Six of these species are known from a single sex: four were described from females and two from males (World Spider Catalog 2023). Only two publications supplemented the single sex species, Tikader (1968) and Ono (2009). When we examined thomisid spider specimens collected by spider enthusiasts from Guangdong and Fujian and borrowed by Dr Guo Tang from the Institute of Zoology, Chinese Academy of Sciences, one new thomisid species was identified as new and is described in this paper, Massuria min sp. nov. Further, we found that the female of Massuria bellula Xu, Han & Li, 2008 is a synonym of the male of Diaea simplex Xu, Han & Li, 2008 and re-combined as Massuria simplex (Xu, Han & Li, 2008) comb. nov.

Materials and methods

Specimens were examined using a SZ6100 stereomicroscope. Both male and female copulatory organs were dissected and examined in 80% ethanol using an Olympus CX43 compound microscope with a KUY NICE CCD camera. Epigynes were cleared with pancreatin solution (Álvarez-Padilla and Hormiga 2007).

The measurements were taken using a stereomicroscope (AxioVision SE64 Rel. 4.8.3) and are given in millimeters. The body lengths of all specimens exclude the chelicerae and spinnerets. Terminology of the male and female genitalia follows Lin et al. (2023). Leg measurements are given as total length (femur, patella, tibia, metatarsus, tarsus). The abbreviations used in the figures and text are as follows:

ALE anterior lateral eye;

AME anterior median eye;

ASM-JGSU Animal Specimen Museum, College of Life Science, Jinggangshan University;

CD copulatory duct;

CO copulatory opening;

d dorsal;

Em embolus;

FD fertilization duct;

IZCAS Institute of Zoology, Chinese Academy of Sciences;

MOA median ocular area;

MP median plate;

p prolateral;

PLE posterior lateral eye;

PME posterior median eye;

r retrolateral;

RTA retrolateral tibial apophysis;

Spe spermatheca;

v ventral;

VTA ventral tibial apophysis.

Taxonomy

Family Thomisidae Sundevall,1833

Genus Massuria Thorell, 1887

Massuria bandian Tang & Li, 2010

Figs 1, 2

Massuria bandian Tang & Li, 2010b: 29, figs 18A–D, 19A–B (holotype not examined).

Material examined

1f, 9 m: China: Hainan Province: Ledong County, Jianfengling National Natural Reserve, Mingfenggu Scenic Spot, 18°44'25.87"N, 108°50'47.83"E, 14 August 2010, G. Zheng leg. (Tho-132, HUN).

Diagnosis

The females of this species resemble that of Massuria min sp. nov. (Fig. 5A, C, D) in having a triangular median plate, but differs from it by the carapace lacking dots (vs. present), the slightly parallel copulatory ducts (vs. W-shaped) and the C-shaped spermathecae (vs. fan-shaped) (Fig. 1A, C, D). Male can be easily distinguished from other Massuria species (Xu et al. 2008; Tang and Li 2010b; Lin et al. 2023) by the legs I and II lacking annulations (vs. present), the retrolateral tibial apophysis lacking basal apophysis (vs. present) and the embolus arising from a 3 o’clock (vs. other positions).

Figure 1. 

Massuria bandian Tang & Li, 2010, female A habitus, dorsal view B same, ventral view C epigyne, dorsal view D same, ventral view. Abbreviations: CD – copulatory duct, CO – copulatory opening, FD – fertilization duct, MP – median plate, Spe – spermatheca. Scale bars: 0.5 mm (A, B); 0.1 mm (C, D).

Description

Female. Habitus (Fig. 1A, B). Total length 5.85. Carapace length 2.37, width 2.69, with many short club-shaped setae. Eye diameters and interdistances: AME 0.05, ALE 0.09, PME 0.05, PLE 0.07; AMEAME 0.25, ALEAME 0.18, ALEALE 0.67, PMEPME 0.23, PLEPME 0.35, PLEPLE 1.02, AMEPME 0.27, AME-PLE 0.47, ALEPLE 0.20, MOA 0.36 long, front width 0.35, back width 0.33. Chelicerae yellow, straight, robust, with several thick setae on frontal surface, lacking promarginal and retromarginal teeth. Endites yellow, with a distinct constriction medially, anterolaterally fan-shaped. Labium oval, longer than 2/3 of endite. Sternum (Fig. 1B) yellow, broadly oval, slightly longer than wide. Legs yellow (Fig. 1A, B), without annulation, measurements (Fig. 1A, B): I 8.75 (2.8, 1.44, 2.37, 1.41, 0.73); II 9.08 (2.74, 1.51, 2.41, 1.67, 0.75); III 5.36 (1.7, 0.82, 1.3, 0.91, 0.63); IV 5.05 (1.99, 0.83, 1.27, 0.55, 0.41); setation (Fig. 1A, B): I Fe: d1, p1; Pa: d1; Ti: v8; Mt: p2, r1, v12; II Pa: d1; Pa: d1; Ti: v8; Mt: p1, r1, v12; III Ti: d1; Mt: d1; IV: Ti: d1; Mt: d1. Abdomen (Fig. 1A, B): length 3.48, width 3.22, with a yellow cross-shaped mark on anteromedial abdomen.

Epigyne (Fig. 1C, D). Median plate (MP) triangular, copulatory openings (CO) located posterolateral of median plate. Copulatory ducts (CD) relatively long, as long as spermathecal length, slightly separated. Spermathecae (Spe) sac-shaped, slightly curved, with several constrictions. Fertilization ducts (FD) short and broad, directed laterally.

Male. Habitus (Fig. 2A, B). As in female except as follows. Total length 3.53. Carapace (Fig. 2A) length 1.56, width 1.73, with several erect club-shaped setae. Eye (Fig. 2A) diameters and interdistances: AME 0.06, ALE 0.10, PME 0.05, PLE 0.09; AMEAME 0.16, AMEALE 0.11, ALEALE 0.47, PMEPME 0.14, PMEPLE 0.25, PLEPLE 0.74, ALEPLE 0.16, AMEPME 0.18. MOA 0.29 long, front width 0.26, back width 0.26. Chelicerae yellow, straight, robust, with abundant thick setae on frontal surface, lacking promarginal and retromarginal teeth. Endites yellow, with a distinct constriction medially. Labium trapezoidal. Legs yellow (Fig. 2A, B), legs I and II without annulations on patellae, tibiae, metatarsi, and tarsi; measurements: I 8.86 (2.7, 0.84, 2.25, 1.96, 1.11); II 7.67 (1.9, 0.82, 2.3, 1.84, 0.81); III 3.2 (0.95, 0.44, 0.82, 0.56, 0.43); IV 3.44 (1.12, 0.54, 0.93, 0.45, 0.4); setation (Fig. 2A, B): I Ti: d2, p1, r2, v5; Mt: p1, r2, v8; II Fe: d5; Ti: d3, p2, r1, v4; Mt: v10; III Fe: d3; Pa: d1; Ti: d3; IV: Fe: d2; Pa: d1, r1; Ti: d4; Mt: p1, r1. Abdomen (Fig. 2A, B) oval, 1.97 long, 1.19 wide, yellowish to yellow.

Figure 2. 

Massuria bandian Tang & Li, 2010, male A habitus, dorsal view B same, ventral view C palp, prolateral view D same, ventral view E same, retrolateral view. Abbreviations: Em – embolus, RTA – retrolateral tibial apophysis, VTA – ventral tibial apophysis. Scale bars: 0.2 mm (A, B); 0.1 mm (C, D).

Palp (Fig. 2C−E). Ventral tibial apophysis (VTA) slightly shorter than tibia, directed anteriorly. Retrolateral tibial apophysis (RTA) longer than tibia, sub-medial part sharply pointed, with a thick spine-like tip. Embolus (Em) arising from 6 o’clock and ending at about 2 o’clock.

Distribution

Known from Yunnan and Hainan (this article), China (Fig. 7).

Massuria simplex (Xu, Han & Li, 2008), comb. nov.

Figs 3, 4, 6A, B

Pistius gangulyi Yaginuma & Wen, 1983: 193, fig. 1A−C (♀, misidentified).

Diaea simplex Xu, Han & Li, 2008: 14, fig. 1a−e (male holotype not examined). syn. nov.; Tang et al. 2010a (♂).

Massuria bellula Xu, Han & Li, 2008: 15, fig. 2a−c (female holotype not examined).

Material examined

1f, 1 m: China: Guangdong Province: Maoming City, Gaozhou City, Changpo Town, 22°4'43.34"N, 111°6'30.51"E, 6.II.2022, Y.H. Zhong leg. (Tho-297, ASM-JGSU).

Diagnosis

Female resembles those of M. daizong Lin & Li, 2023 (see Lin et al. 2023: 74, figs 66A, B, 67B) in having the sac-shaped spermathecae with many constrictions, but can be easily differentiated from it by the dorsal abdomen without a distinct marking (vs. a red face mask-like marking present in M. daizong), the W-shaped epigynal plate (vs. M-shaped in M. daizong), and the long longitudinal copulatory ducts (vs. short in M. daizong) (Fig. 3C, D). Male is very similar to that of Massuria ovalis Tang & Li, 2010 (see Tang and Li 2010b: 29, fig. 21A, B) in having a long embolus (Em) arising and ending at the 3 o’clock position of the tegulum, but can be recognized by the straight ventral tibial apophysis (VTA) (vs. slightly curved in M. ovalis) and the retrolateral tibial apophysis (RTA) with a ridge-like apophysis near the base (vs. lacking basal apophysis in M. ovalis) and thick spine-like apex (vs. very blunt in M. ovalis) in ventral view (Fig. 4G, H).

Figure 3. 

Massuria simplex (Xu, Han & Li, 2008) comb. nov., female A habitus, dorsal view B same, ventral view C epigyne, dorsal view D same, ventral view. Abbreviations: CD – copulatory duct, CO – copulatory opening, FD – fertilization duct, MP – median plate, Spe – spermatheca. Scale bars: 1 mm (A, B); 0.1 mm (C, D).

Figure 4. 

Massuria simplex (Xu, Han & Li, 2008) comb. nov., male A habitus, dorsal view B same, ventral view C carapace, frontal view D left leg I, prolateral view E palp, ventro-prolateral view F same, ventral view G same, ventro-retrolateral view H same, dorsal view. Abbreviations: Em – embolus, RTA – retrolateral tibial apophysis, VTA – ventral tibial apophysis. Scale bars: 0.5 mm (A, B); 0.2 mm (D); 0.1 mm (C, E–H).

Description

Female. Habitus (Figs 3A, B, 6A, B). Total length 8.07. Carapace length 3.72, width 3.52. Eye diameters and interdistances: AME 0.09, ALE 0.11, PME 0.07, PLE 0.09; AMEAME 0.41, ALEAME 0.30, ALEALE 1.06, PMEPME 0.40, PLEPME 0.50, PLEPLE 1.48, AMEPME 0.40, AME-PLE 0.70, ALEPLE 0.29, MOA 0.54 long, front width 0.53, back width 0.54. Leg without annulation, measurements (Fig. 3A, B): I 11.6 (3.43, 1.76, 2.87, 2.32, 1.22); II 11.79 (3.65, 1.76, 2.8, 2.37, 1.21); III 5.95 (2.17, 0.79, 1.37, 1.04, 0.58); IV 6.46 (2.3, 0.69, 1.4, 1.34, 0.73); setation (Fig. 3A, B): I Fe: d4; Ti: v8; Mt: p3, r1, v16; II Pa: d1; Ti: v5; Mt: p2, r1, v13; III Ti: d3; Mt: d3, p2; IV: Ti: d3. Abdomen (Fig. 3A, B): length 4.35, width 4.98, with a brown linear mark on anteromedial abdomen.

Epigyne (Fig. 3C, D). Median plate (MP) W-shaped, copulatory openings (CO) located laterally. Copulatory ducts (CD) very short, as long as 1/3 of spermathecal length. Spermathecae (Spe) sac-shaped, median thinner than anterior and posterior parts, with several constrictions. Fertilization ducts (FD) short and broad, directed laterally.

Male. Habitus (Fig. 4A−C). Total length 3.45. Carapace (Fig. 4A) broadly oval, length 1.70, width 1.82, with densely granulated trichopores. Eye (Fig. 4C) diameters and interdistances: AME 0.07, ALE 0.09, PME 0.05, PLE 0.07; AMEAME 0.22, AMEALE 0.15, ALEALE 0.61, PMEPME 0.22, PMEPLE 0.29, PLEPLE 0.88, ALEPLE 0.19, AMEPME 0.20. MOA 0.31 long, front width 0.31, back width 0.33. Chelicerae yellow, straight, robust, with abundant thick setae on frontal surface, lacking promarginal and retromarginal teeth. Endites yellow, with a distinct constriction medially. Labium oval, as long as 2/3 of endite. Sternum (Fig. 4B) yellow, broadly oval, wider than long. Legs yellow (Fig. 4A, B), legs I and II with brown annulations on patellae, tibiae, metatarsi, and tarsi; measurements: I 6.68 (2.04, 0.84, 1.58, 1.38, 0.84); II 6.99 (2.06, 0.87, 1.7, 1.48, 0.88); III 3.52 (0.97, 0.54, 0.88, 0.69, 0.44); IV 3.13 (0.9, 0.59, 0.82, 0.5, 0.32); setation (Fig. 4A, B): I Fe: d3, p4; Ti: d1, v4; Mt: p1, r1, v10; II Fe: d5; Ti: d1, v4; Mt: p2, r2, v6; III Fe: d2; Pa: d2; Ti: d1; IV: Fe: d2; Pa: d2, r1; Ti: d4, r1. Abdomen (Fig. 4A, B) ovoid, 1.75 long, 1.72 wide, yellow, laterally with arc-shaped filiform mark.

Palp (Fig. 4E−H). Ventral tibial apophysis (VTA) slightly shorter than tibia, directed retrolaterally. Retrolateral tibial apophysis (RTA) longer than tibia, with a ridge-like apophysis and a thick spine-like tip. Embolus (Em) arising from 3 o’clock and ending at the same position.

Comments

It is noteworthy that the figure of the female of Pistius gangulyi presented by Yaginuma and Wen (1983) agreed well with the specimens known from Guangdong, although they had a female specimen from Hainan as the same as the male records by Tang and Li (2010a). While the holotype female of Massuria bellula Xu, Han & Li, 2008 was collected from the Tai Lung Experimental Station, Hong Kong, China by Ping-wing Chan on 30 June 1999. The male of Diaea simplex Xu, Han & Li, 2008 was also discovered by him a week later from the same locality. The latter is the same species as the first because it has all of the diagnostic features of Massuria: the pentagonal abdomen with distinct submarginal pattern and the male palpal RTA modified into a distal process (Sen et al. 2015). Further examination of the male and female genitalia in this study confirms its synonymy with Diaea simplex Xu, Han & Li, 2008 (compare Fig. 1 with Xu et al. 2008: 14, fig. 1) and the records of Pistius gangulyi from Hainan in Yaginuma and Wen (1983) were misidentified. The species M. bellula should thus be regarded a synonym of D. simplex Xu, Han & Li, 2008.

Distribution

Known only from Guangdong, Hainan (Yaginuma and Wen 1983; Tang and Li 2010a) and Hong Kong (Xu et al. 2008), China (Fig. 7).

Massuria min Yao & Li, sp. nov.

Figs 5, 6C, D

Type material

Holotype : 1f: China: Fujian Province: Longyan City, Xinluo District, Jiangshan Town, 25°8'20.68"N, 116°58'53.56"E, 307 m, 1.X.2022, L.F. Wei. leg. (Tho-298, ASM-JGSU).

Etymology

The specific name refers to the Chinese abbreviation for Fujian Province; noun in apposition.

Diagnosis

Massuria min sp. nov. is similar to M. bandian Tang & Li, 2010 (Fig. 1A, C, D) and M. uthoracica Sen, Saha & Raychaudhuri, 2012 (see Sen et al. 2015: 64, figs 334, 337, 338) in having a triangular epigynal plate, but differs from it by the carapace with abundant spots (vs. absent in M. bandian and M. uthoracica), the long W-shaped copulatory ducts combined with a dorsal hood (vs. triangular in M. bandian; absent in M. uthoracica) and the fan-shaped spermathecae (vs. C-shaped in M. bandian; straight in M. uthoracica) (Fig. 5C, D).

Figure 5. 

Massuria min sp. nov., female holotype. A habitus, dorsal view B same, ventral view C epigyne, dorsal view D same, ventral view. Abbreviations: CD – copulatory duct, CO – copulatory opening, FD – fertilization duct, MP – median plate, Spe – spermatheca. Scale bars: 0.5 mm (A, B); 0.1 mm (C, D).

Description

Female. Habitus (Figs 5A, B, 6C, D). Total length 5.31. Carapace (Fig. 5A) with green spots, length 2.24, width 2.30. Eyes (Fig. 5A) diameters and interdistances: AME 0.06, ALE 0.09, PME 0.05, PLE 0.09; AMEAME 0.25, ALEAME 0.16, ALEALE 0.63, PMEPME 0.23, PLEPME 0.33, PLEPLE 0.96, AMEPME 0.25, ALEPLE 0.22. MOA 0.34 long, front width 0.33, back width 0.33. Chelicerae yellow, straight, robust, without retromarginal or promarginal teeth. Endites yellow, medially with distinct constriction. Labium yellow, inverted U-shaped, as long as 2/3 of endite. Sternum pale to yellow, longer than wide. Legs yellow (Fig. 5A, B); measurements: I 8.15 (2.23, 1.14, 2.18, 1.8, 0.8); II 8.42 (2.23, 1.18, 2.25, 1.88, 0.88); III 4.88 (1.52, 0.83, 1.05, 0.95, 0.53); IV 5.06 (1.78, 0.71, 1.03, 0.96, 0.58); setation (Fig. 5A, B): I Fe: d4; Pa: d1; Ti: d2, v8; Mt: d1, p2, v12; II Fe: d1; Pa: d1; Ti: d1, v8; Mt: d1, p2, v11; III Pa: d1; Ti: v1; IV: Pa: d1. Abdomen (Fig. 5A, B) 3.07 long, 2.47 wide, ovoid, silver with yellow cross-shaped marks dorsally, and several yellow dots located anterolaterally.

Figure 6. 

Photographs of living specimens from China A, B Massuria simplex (Xu, Han & Li, 2008) comb. nov., female C, D Massuria min sp. nov., female.

Epigyne (Figs 5C, D). Median plate (MP) triangular, copulatory openings (CO) located at antero-lateral part. Copulatory ducts (CD) W-shaped, extending from median to posterior of vulva and turn back to forward. Spermathecae (Spe) fan-shaped, with several constrictions, widely separated as long as their length. Fertilization ducts (FD) short, directed anteromedially.

Male. Unknown.

Comments

At present, M. ovalis Tang & Li, 2010 is known only from the male in mainland China; therefore, the new species may be conspecific with this species.

Distribution

Known only from the type locality (Fig. 7).

Figure 7. 

Location records of Massuria bandian Tang & Li, 2010, Massuria simplex (Xu, Han & Li, 2008) comb. nov. and M. min sp. nov. from China.

Acknowledgements

We thank Dr Galina N. Azarkina and subject editor Stefan Foord for their helpful suggestions and comments on the manuscript, and Dr Nathalie Yonow for improving the English of the manuscript. We are also grateful to Ling-feng Wei, Yu-hao Zhong (钟宇豪) and Guo Zheng for collecting the specimens and Yu-hao Zhong (钟宇皓) for providing exquisite living photos in field work.

Additional information

Conflict of interest

The authors have declared that no competing interests exist.

Ethical statement

No ethical statement was reported.

Funding

This study was supported by the Natural Science Foundation of China (32000301/32160243/32070429).

Author contributions

Conceptualization: XX, KL, YX. Data curation: YY, CL.

Author ORCIDs

Cong-zheng Li https://orcid.org/0000-0003-3849-8433

Yan-bin Yao https://orcid.org/0000-0002-2560-9299

Yong-hong Xiao https://orcid.org/0000-0002-8074-9366

Xiang Xu https://orcid.org/0000-0001-9485-5373

Ke-ke Liu https://orcid.org/0000-0001-7822-3667

Data availability

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

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