Spiricoelotes metyr, Chen & Liu & Wei, 2025

Chen, Hailun, Liu, Jie & Wei, Mian, 2025, Two new cave-dwelling Spiricoelotes species (Araneae, Agelenidae) from Hubei, China, ZooKeys 1245, pp. 383-397 : 383-397

publication ID

https://doi.org/10.3897/zookeys.1245.145389

publication LSID

lsid:zoobank.org:pub:9CBA31DA-4DE6-4290-9698-7158DA7B7AFC

DOI

https://doi.org/10.5281/zenodo.16042248

persistent identifier

https://treatment.plazi.org/id/E00578BA-7DB4-5B90-A80E-B4440B5F45D7

treatment provided by

ZooKeys by Pensoft

scientific name

Spiricoelotes metyr
status

sp. nov.

Spiricoelotes metyr sp. nov.

Figs 1 View Figure 1 , 2 View Figure 2 , 4 A, B View Figure 4 , 7 A, B View Figure 7 , 8 View Figure 8

Type materials.

Holotype • ♂ ( CBEE, LJ 202369 ), China: Hubei Province: Xianning City, Chongyang County, dark zone of Daquan Cave , 29.5534°N, 114.2662°E, elevation: 124 m, 31.X.2023, Jian Chang, Mian Wei, Guoyuan Zhang and Haosiyi Zhu leg. GoogleMaps Paratypes: • 3 ♂♂ 3 ♀♀ ( CBEE, LJ 202370 LJ 202375 ), same data as holotype GoogleMaps ; • 4 ♂♂ 5 ♀♀ ( CBEE, LJ 202376 LJ 202384 ), China: Hubei Province: Xianning City, Xianan District, dark zone of a nameless cave , 29.7715°N, 114.3122°E, elevation: 89 m, 10.XII.2023, Jian Chang, Guolong Huang and Mian Wei leg. GoogleMaps

Etymology.

The species name is derived from “ Metyr ”, a character in the myth of Elden Ring, written by George R. R. Martin. Metyr is depicted as having a massive, finger-shaped body and living in an underground cave; this name refers to the shape of the spermathecae and the habitat of this new species. It is treated as a noun in genitive case.

Diagnosis.

The males of Spiricoelotes metyr sp. nov. can be easily distinguished from all other congeners in 1) having a leaf-shaped conductor in dorsal view, with the distal tip of the conductor thin, long, and pointed downward (Fig. 1 A, B View Figure 1 ), versus being not leaf-shaped, sometimes coiled, but always pointed upward in other congeners (Fig. 3 B, E View Figure 3 ; fig. 25 in Shimojana 1989; figs 1 B, 3 B, 5 B, 7 B, 9 B in Chen et al. 2016); 2) the patellar apophysis extremely strong and long (Fig. 1 B, C View Figure 1 ), versus being relatively thin and short in other congeners (Fig. 3 C, F View Figure 3 ; fig. 25 in Shimojana 1989; figs 1 C, 3 C, 5 C, 7 C, 9 C in Chen et al. 2016); 3) the cymbial furrow extremely long, approximately 4 / 5 the length of the cymbium (Fig. 1 C View Figure 1 ), versus being subequal to or less than 1 / 2 the length of the cymbium in other congeners (Fig. 3 C, F View Figure 3 ; fig. 25 in Shimojana 1989; figs 1 C, 3 C, 5 C, 7 C, 9 C in Chen et al. 2016). The females of the new species resemble those of S. xiongxinensis in 1) having laterally situated copulatory openings that are far apart, and extremely short copulatory ducts (Fig. 2 A, B View Figure 2 ; fig. 11 A, B in Chen et al. 2016); 2) shallow and wide hoods (Fig. 2 A View Figure 2 ; fig. 11 A in Chen et al. 2016); 3) spermathecae that are not coiled, with the length of the spermatheca being subequal to the length of the epigynal plate (Fig. 2 B View Figure 2 ; fig. 11 B in Chen et al. 2016). In other congeners, the copulatory openings are situated relatively medially and are close to each other (Figs 5 A, B View Figure 5 , 6 A, B View Figure 6 ; figs 28, 29 in Shimojana 1989; figs 2 A, B, 6 A, B, 8 A, B, 10 A, B in Chen et al. 2016), or laterally situated but with long copulatory ducts in S. chufengensis (fig. 4 A, B in Chen et al. 2016); the hoods deep and thin (figs 5 A, 6 A; fig. 28 in Shimojana 1989; figs 2 A, 4 A, 6 A, 8 A, 10 A in Chen et al. 2016); the spermathecae coiled (Figs 5 B View Figure 5 , 6 B View Figure 6 ; fig. 29 in Shimojana 1989), or not coiled but less than half the length of the epigynal plate (figs 2 B, 4 B, 6 B, 8 B, 10 B in Chen et al. 2016). But the new species can be differentiated from S. xiongxinensis in having relatively thin, regularly shaped spermathecae (Fig. 2 B View Figure 2 ), versus thick and irregularly shaped in S. xiongxinensis (fig. 11 B in Chen et al. 2016).

Description.

Male holotype (Fig. 7 A View Figure 7 ). Carapace yellowish, cervical and radial grooves indistinct. Chelicerae with 3 promarginal teeth and 5 retromarginal teeth, condyle weak. Sternum longer than wide. Abdomen nearly white, without patterns, covered by blueish gray hairs. Legs yellowish. Total length 6.70. Carapace 3.86 long, 2.69 wide. Abdomen 2.78 long, 1.82 wide. Eye diameters and interdistances: AME 0.16, ALE 0.13, PME 0.15, PLE 0.12; AME – AME 0.07, AME – ALE 0.08, PME – PME 0.14, PME – PLE 0.10. Measurements of legs: I 14.81 (4.06, 1.27, 3.50, 3.68, 2.30), II 13.04 (3.68, 1.14, 3.26, 2.73, 2.23), III 13.00 (3.49, 0.68, 2.92, 3.74, 2.17), IV 16.25 (4.32, 0.82, 4.38, 4.16, 2.57).

Palp (Fig. 1 View Figure 1 ). Patellar apophysis long, as twice long as the length of patella. Retrolateral tibial apophysis subequal to the length of tibia. Lateral tibial apophysis short, subequal to 1 / 5 the length of retrolateral tibial apophysis. Cymbial furrow long, subequal to 4 / 5 the length of cymbium. Conductor leaf-shaped from ventral view; ventral margin short and strongly sclerotized; dorsal margin wide, distal tip thin and long, pointed downward, with developed membranous ridge; apophysis of dorsal margin broad and ridge-shaped. Tegular ridge slice-shaped and situated retroalterally, matched with the ridge-shaped dorsal apophysis of conductor. Embolus arising in a 4: 00–4: 30 o’clock-position, extremely long. Median apophysis reduced.

Female paratype (Fig. 7 B View Figure 7 ). Same in colour, abdominal patterns, and chelicera teeth as male. Total length 7.89. Carapace 3.99 long, 2.56 wide. Abdomen 3.67 long, 2.61 wide. Eye diameters and interdistances: AME 0.15, ALE 0.14, PME 0.16, PLE 0.15; AME – AME 0.09, AME – ALE 0.11, PME – PME 0.11, PME – PLE 0.10. Measurements of legs: I 13. 56 (3.53, 1.16, 3.04, 3.56, 2.27), II 12. 52 (3.37, 1.31, 3.12, 2.92, 1.80), III 11. 42 (3. 17, 0.48, 2.90, 3.30, 1.57), IV 16. 13 (4.14, 0.97, 3.82, 4.81, 2.39).

Epigyne (Fig. 2 View Figure 2 ). Epigynal plate wider than long. Copulatory openings situated laterally and separated from each other. Hoods located anteriorly. Copulatory ducts extremely short. Spermathecal heads small, situated near the beginning of spermathecal stalks; spermathecae curved-finger-shaped, with smooth surface and with extremely coiled duct inside. Fertilization ducts short, posteriorly situated.

Variation.

The deep hoods appear in only one female individual from Daquan Cave, and we consider it to be a mutation.

Distribution.

Only known from the type localities (Fig. 8 View Figure 8 ).

Kingdom

Animalia

Phylum

Arthropoda

Class

Arachnida

Order

Araneae

Family

Agelenidae

Genus

Spiricoelotes