Acantheis andreimishenini, Fomichev & Omelko & Marusik, 2023
publication ID |
https://doi.org/ 10.11646/zootaxa.5353.2.2 |
publication LSID |
lsid:zoobank.org:pub:7A24DCBF-BC93-4B25-BB8A-DEAE75167DB4 |
DOI |
https://doi.org/10.5281/zenodo.8427168 |
persistent identifier |
https://treatment.plazi.org/id/0396878D-F55B-6C7B-3EA3-A5C1F4FBFB9B |
treatment provided by |
Plazi |
scientific name |
Acantheis andreimishenini |
status |
sp. nov. |
Acantheis andreimishenini sp. n.
Figs 3–6 View FIGURES 1–6 , 10–11 View FIGURES 7–11 , 17–21 View FIGURES 12–21 , 26–29 View FIGURES 22–29 , 31–35 View FIGURES 30–35 , 46–48 View FIGURES 46–48
Types. INDONESIA: Sumatra Island: Aceh Prov.: holotype ♁ ( ISEA, 001.9532), Kedah Vil. [03°59′N, 97°15′E], 1300–1500 m, 1988 (precise date unknown), unknown collector GoogleMaps . Paratypes: 3♁ ( ISEA, 001.9533), 1♀ ( ISEA, 001.9534), together with the holotype .
Etymology. The species name is a patronym given in honor of the teacher and friend of Alexander A. Fomichev, Andrei I. Mishenin (Novosibirsk, Russia), brother of Sergei I. Mishenin, on the occasion of his 60th anniversary.
Diagnosis. This new species is similar to A. laetus from Kalimantan and to A. sergeimishenini sp. n. and A. dimidiatus from Sumatra in having a slender embolus (Em), a medially located tegular apophysis (TA) and an elongated cymbial tip. The male can be easily distinguished from that of A. laetus by the strongly curved embolus (vs. smoothly rounded, cf. Fig. 27 View FIGURES 22–29 and Lehtinen 1967: fig. 410), and from that of A. sergeimishenini sp. n. by the smaller body size (carapace length 5.8 vs. 7.7), the shorter bulb (1.03 mm vs. 1.32 mm), the non-bifurcated retrolateral tibial apophysis (RTA) (vs. bifurcated, cf. Figs 20 and 15 View FIGURES 12–21 ), the round tegular apophysis (seen in ventral view; vs. comma-shaped, cf. Figs 27 and 23 View FIGURES 22–29 ) and the ventral (VB) and dorsal (DB) branches of the embolus with the same width (vs. the ventral branch twice as wide as the dorsal one, cf. Figs 31 and 30 View FIGURES 30–35 ). The male of A. andreimishenini sp. n. differs from that of A. dimidiatus by the wide cardiac mark reaching middle part of opisthosoma (vs. thin stripe reaching spinnerets, cf. Figs 3 View FIGURES 1–6 and 36 View FIGURES 36–44 ), the median band on the carapace as wide as the distance between PLE (vs. as wide as distance between PME), the circular tegular apophysis (vs. triangular, cf. Figs 27 View FIGURES 22–29 and 43 View FIGURES 36–44 ), and the dorsal and ventral embolic branches equal in size (vs. ventral embolic branch twice thinner than dorsal one, cf. Figs 31 View FIGURES 30–35 and 41 View FIGURES 36–44 ). For a complete list of the differences between the males of A. andreimishenini sp. n., A. sergeimishenini sp. n. and A. dimidiatus , see Table 7 View TABLE 7 . The female of A. andreimishenini sp. n. is similar to that of A. indicus Gravely, 1931 from India, in having the rectangular septal base (SB), but differs in having parallel epigynal teeth (ET) (vs. converging), the posterior part of septal base with rounded angles (vs. sharp), and a wide gap between epigynal teeth and septal base (vs. narrow, cf. Figs 32–33 View FIGURES 30–35 and Gravely 1931: fig. 3D).
Description. Male (holotype). Total length 11.5, carapace 5.8 long, 5.2 wide. Opisthosoma 6.1 long, 3.5 wide. Eye sizes and interdistances: AME 0.39, ALE 0.2, PME 0.46, PLE 0.43, AME–AME 0.17, AME–ALE 0.26, PME– PME 0.21, PME–PLE 0.29, AME–PME 0.14, ALE–PLE 0.23. Clypeus height at AME 0.49, at ALE 0.93. Labium as long as wide. For palp and legs measurements see Table 3 View TABLE 3 . For palp and leg spination see Table 4. Coloration ( Figs 3–4 View FIGURES 1–6 , 10 View FIGURES 7–11 ), carapace brown, with yellow median band. Clypeus and chelicerae dark brown. Labium and endites brown. Sternum and coxae yellow. Palps and legs yellow-brown, with grey annulations. Opisthosoma dorsally yellow-gray, with yellow cardiac mark. Posterior part of opisthosoma bears several clusters of stiff yellow setae. The venter dirty yellow. Spinnerets yellow-grey.
Male palp as shown in Figs 17–21 View FIGURES 12–21 , 26–29 View FIGURES 22–29 , 31 View FIGURES 30–35 . Tibia ca. 4.5 longer than wide, with five very long spines, the longest is about 0.7 times of tibia length. Retrolateral tibial apophysis (RTA) small, non-bifurcated. Cymbium length/width ratio ca. 2.4. Tip of cymbium about 0.39 of cymbial length, sligthly shorter than bulb. Bulb 1.25 times longer than cymbial apex. Subtegulum (St) oval. Tegular length/width ratio ca. 1.4. Sperm duct (SD) clearly visible only in retrolateral view. Retrolateral margin of tegular process (TP) concave. Tegular apophysis almost round. Conductor (Cn) 2.4 times longer than wide, covering embolic tip. Embolic base with basal process (BP) located near subtegular notch (SN). Membranous extension of embolus (ME) thinner than its adjoining part. Embolus (Em) strongly curved, with a small spike (ES) ventrally. Dorsal branch (DB) of embolus as wide as ventral one (VB).
Female. Total length 14.86, carapace 6.38 long, 5.42 wide. Opisthosoma 8.32 long, 5.66 wide. Eye sizes and interdistances: AME 0.37, ALE 0.23, PME 0.46, PLE 0.48, AME–AME 0.22, AME–ALE 0.34, PME–PME 0.23, PME–PLE 0.35, AME–PME 0.20, ALE–PLE 0.25. Clypeus height at AME 0.53, at ALE 1.05. For palp and legs measurements see Table 5. For palp and legs spination see Table 6 View TABLE 6 . Coloration ( Figs 5–6 View FIGURES 1–6 , 11 View FIGURES 7–11 ), carapace, clypeus, chelicerae, labium and endites as in the male. Sternum and coxae brown. Palps and legs as in the male, but with more contrasting annulations. Opisthosoma as in the male, but somewhat lighter, its posterior part bears several clusters of stiff yellow setae.
Female genitalia as shown in Figs 32–35 View FIGURES 30–35 . Epigyne slightly wider than long. Septal base (SB) almost square, with heavily sclerotized septal humps (SH). Septal stem (SS) 1.5 times shorter than septal base. Epigynal teeth (ET) parallel, as long as septal stem. Receptacles (Re) subdivided into two chambers: chamber I (RI) and chamber II (RII), both are about of the same size.
Distribution. Only known from the type locality ( Figs 46–48 View FIGURES 46–48 ).
ISEA |
Poland, Krakow, Polish Academy of Sciences, Institute of Systematic Zoology |
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.