Anemesia karatauvi ( Andreeva, 1968 )
publication ID |
https://doi.org/ 10.5852/ejt.2018.485 |
publication LSID |
lsid:zoobank.org:pub:55A0F74D-FA80-4C6A-AD74-B49C9061A449 |
DOI |
https://doi.org/10.5281/zenodo.3848293 |
persistent identifier |
https://treatment.plazi.org/id/03D05632-DF2E-9753-CE23-FC12FBB80C3C |
treatment provided by |
Valdenar |
scientific name |
Anemesia karatauvi ( Andreeva, 1968 ) |
status |
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Anemesia karatauvi ( Andreeva, 1968) View in CoL
Figs 9 View Figs 1–9 , 22 View Figs 18–26 , 31 View Figs 27–33 , 56 View Figs 48–62 , 71 View Figs 63–77 , 83 View Figs 78–89 , 98 View Figs 90–98 , 111 View Figs 108–116 , 126 View Figs 125–132 , 145–146 View Figs 143–157 , 169–170 View Figs 158–172 , 181 View Figs 173–187 , 209–210 View Figs 206–214 , 246–249 View Figs 245–265 , 280–281 View Figs 278–290 , 298–301, 313, 317, 333–336, 362, 371 View Fig
Brachythele karatauvi Andreeva, 1968: 70 , fig. 2a–b (Ƌ ♀).
Brachythele karatauvi – Andreeva 1976: 14, figs 6–7 (Ƌ ♀). — Brignoli 1983: 123. — Fet 1984: 40. — Zonstein 1985: 159; 1987: 1013.
Anemesia karatauvi View in CoL – Mikhailov 1996: 77; 1997: 20. — Zonstein 2001: 11; 2004: 352, fig. 6 (♀). — Marusik et al. 2014: 3, fig. 10 (Ƌ).
Diagnosis
Males of Anemesia karatauvi differ from those of A. castanea sp. nov. by a stouter male palpal tibia, a flattened ventral surface of the palpal bulb and a shorter embolus (vs a slender tibia, a domed surface, and a longer embolus; Figs 181 View Figs 173–187 , 209–210 View Figs 206–214 , cf. Figs 180 View Figs 173–187 , 206–208 View Figs 206–214 ). Females of A. karatauvi can be distinguished from those of A. castanea sp. nov. in having less diverged spermathecae which arise more distantly from each other ( Figs 246–249 View Figs 245–265 , cf. Fig. 245 View Figs 245–265 ), by relatively larger AME and ALE ( Fig. 71 View Figs 63–77 , cf. Fig. 70 View Figs 63–77 ), by a lesser number of the maxillary cuspules (40–55 vs 65–70) and by a weaker cheliceral rastellum.
Type material
Holotype
TAJIKISTAN: Ƌ, Vahsh Karatau Mts. , no locality data, 23–25 Apr. 1967, E. Andreeva leg. (absent in the type series of Brachythele karatauvi kept in MIZW, seems lost and thus not examined)..
Paratypes
TAJIKISTAN: 7 ♀♀, same collection data as for the holotype ( MIZW; examined). See notes below.
Additional material examined (2 ƋƋ, 25 ♀♀) TAJIKISTAN: 1 Ƌ, 6 ♀♀, western slope of Vahsh Karatau Mts, 950–1200 m, 38°01′ N, 68°57′ E, 3 km
NNW of Mt Hojamaston, 21–25 Apr. 1989, S. Zonstein leg. ( SMNH); 1 Ƌ, 5 ♀♀, same collection data as for preceding but 26 Apr. 1990 ( SMNH); 3 ♀♀, Vahsh Karatau Mts, 1.5 km W of Mt Hojamaston, 1040 m, 38°04.6′ N, 68°57.2′ E, 24 Apr. 2015, S. Zonstein leg. ( SMNH); 9 ♀♀, Vahsh Karatau Mts, Chimsai Gorge, 700–1200 m, 38°00′ N, 68°56′ E, 22 Apr. 1986, S. Zonstein and A. Zyuzin leg. ( SMNH); 2 ♀♀, foothills 3 km SE of Yavan, 800–1000 m, 38°18′ N, 69°05′ E, 19 Apr. 1988, S. Zonstein leg. ( SMNH).
Description
Male (from Mt Hojamaston area)
HABITUS. See Fig. 9. View Figs 1–9
MEASUREMENTS. TBL 13.10, CL 5.95, CW 5.07, LL 0.63, LW 1.05, SL 2.77, SW 2.53.
COLOUR IN ALCOHOL. Carapace medium foxy brown with anterior edge darker and thoracic part lighter: chelicerae, most part of palps and legs light yellowish brown; sternum, labium, maxillae and leg tarsi paler; eye tubercle blackened; abdomen dorsally yellowish grey with brown pattern consisting of moderately wide median stripe and few paired transverse and slightly inclined short stripes, ventral part of abdomen pale yellowish grey, spinnerets pale brownish yellow.
PROSOMA. Clypeus and eye tubercle as in Fig. 56 View Figs 48–62 . Eye diameters and interdistances: AME 0.16(0.22), ALE 0.23, PLE 0.19, PME 0.16, AME–AME 0.22(0.16), ALE–AME 0.14(0.11), ALE–PLE 0.14, PLE– PME 0.02, PME–PME 0.49. Cheliceral rastellum consists of 20–25 spikes grouped in one transverse row. Each cheliceral furrow with 7 promarginal teeth and 4 smaller retromarginal teeth. Sternum, labium and maxillae as shown in Fig. 98 View Figs 90–98 . Sternal sigilla small oval, posterior pair considerably distant from sternum edge. Maxillae with 30–32 cuspules each.
LEGS. Tibia and metatarsus I as in Fig. 126 View Figs 125–132 . Scopula: distal and entire on metatarsi I and II, narrowly divided on tarsi I and II, widely divided on tarsi III, absent on tarsi IV. Trichobothria: 2 rows of 8–9 each on tibiae, 12–14 on metatarsi, 12–15 on tarsi, 7 on cymbium. PTC I–II with 7 teeth on each margin. PTC III–IV with 8 teeth on outer and 5–6 teeth on inner margin.
SPINATION. Palp: femur d4, pd3, rd1; patella pd1; tibia d1, p3, r1, pv2, v6; tarsus d13–16. Leg I: femur d5, pd3, rd1; tibia pd4, p1, r3, v8+m; metatarsus d1, pd2, v6. Leg II: femur d5, pd3, rd1; tibia p3, v8; metatarsus p3, v7. Leg III: femur d4, pd3, rd3; patella p3, r2; tibia d1, p3, r3, v8; metatarsus pd4, p3, r2, v9; tarsus pv3. Leg IV: femur d5, p3, r3; tibia d1, p3, r3, v8; metatarsus pd2, p3, r7, v7; tarsus p2. Patellae I, II and IV, and tarsi I and II aspinose.
PALP. Tibia, cymbium and palpal organ as shown in Figs 181 View Figs 173–187 , 209–210 View Figs 206–214 . Palpal tibia long, slender, and slightly swollen, with numerous stout bristles ( Fig. 181 View Figs 173–187 ). Palpal organ with embolus tapering and slightly curved ( Figs 209–210 View Figs 206–214 ).
SPINNERETS. See Fig. 280 View Figs 278–290 . PMS: length 0.51, diameter 0.22. PLS: maximal diameter 0.53; length of basal, medial and apical segments 0.90, 0.65, 0.83; total length 2.38; apical segment shortly digitiform.
Female (from Mt Hojamaston area)
HABITUS. See Fig. 22. View Figs 18–26
MEASUREMENTS. TBL 23.50, CL 8.07, CW 7.45, LL 0.88, LW 1.53, SL 4.35, SW 3.87.
COLOUR. Similar to that of male, but darker: caput, palps and anterior legs chestnut-brown; chelicerae dark copper-brown; dorsal abdominal pattern dark brown; in addition to setae, chelicerae covered with tiny copper-coloured iridescent hairs.
PROSOMA. Clypeus and eye tubercle as shown in Fig. 71 View Figs 63–77 . Eye diameters and interdistances: AME 0.18(0.25), ALE 0.33, PLE 0.22, PME 0.18, AME–AME 0.24(0.18), ALE–AME 0.20(0.17), ALE–PLE 0.20, PLE–PME 0.04, PME–PME 0.75. Cheliceral rastellum represented by approximately 20 spikes located in front of fang base and on low mound. Each cheliceral furrow with 7 promarginal teeth and 7 smaller retromarginal teeth (see Fig. 83 View Figs 78–89 ). Sternum, labium and maxillae as shown in Fig. 111 View Figs 108–116 . Sternal sigilla small; posterior pair distant from sternum edge, oval, or of irregular shape, but anyway extended. Maxillae with 43–52 cuspules each.
LEGS. Scopula dense, occupies 5/6 ventral surface of metatarsus I, distal on metatarsus II, entire on palpal tarsus and tarsi I–II, elsewhere absent. Trichobothria: 2 rows of 8–12 each on tibiae, 14–18 on metatarsi, 14–18 on leg tarsi, 12 on palpal tarsus. Palpal claw with 3–4 promarginal teeth. PTC I–III with 5–6 teeth on outer, 4–6 teeth on inner margin; PTC IV with 5–6 and 2–3 teeth, respectively.
SPINATION. Palp: femur pd1; patella d1, p1, pv1, rv2–3; tibia p2, v13–14; tarsus p1, v2–3. Leg I: femur pd1; tibia p1, v4; metatarsus v6. Leg II: femur pd1; tibia p3, v6–7; metatarsus p1, v6. Leg III: femur pd1–3, rd3; patella p3; tibia d1, p3, r1, v6–7; metatarsus pd2, p4, rd3, v7; tarsus p2. Leg IV: femur rd1; tibia rd2, v6–7; metatarsus pd1, p2, rd2, v8–9; tarsus v1. All femora except dorsal row of bristles with 1 basodorsal spine; patellae I, II, and IV, and tarsi I and II aspinose.
SPERMATHECAE. Normally entire with stalks narrowed subapically ( Fig. 246 View Figs 245–265 ).
SPINNERETS. See Fig. 281 View Figs 278–290 . PMS: length 0.83, diameter 0.35. PLS: maximal diameter 0.85; length of basal, medial and apical segments 1.45, 0.87, 0.85; total length 3.63; apical segment shortly digitiform.
Variation
The length of carapace varies from 5.78 to 5.90 in males and from 5.82 to 9.23 in females. The colouration varies through specimens very narrowly. The number of maxillary cuspules ranges from 28 to 32 in males and from 40 to 55 in females. No significant variation in structure of the palpal organ is evident. The spermathecae are generally uniform ( Figs 246, 248–249 View Figs 245–265 ); however, occasionally the stalks are divided subapically (see Fig. 247 View Figs 245–265 ).
Habitats
The species occurs in woodless steppe foothills at 700–1000 m, as well as in the scarcely forested midland area above, with shrubs and low trees represented by Acer , Prunus and Pistacia (see Figs 313 View Figs 306–313 , 317 View Figs 314–321 ).
Distribution
Contrary to the distribution provided with the original description, the range of this species is confined to the Vahsh Karatau Mts in southwestern Tajikistan only, as shown in Fig. 371 View Fig (see below).
Notes
A captured live male is shown in Fig. 31 View Figs 27–33 (a positive slide made in 1989). The cheliceral rastellum, trichobothrial bases and tarsal organ of leg I, and spigots are shown in Figs 145–146 View Figs 143–157 , 169–170 View Figs 158–172 , and 298–301, respectively.
Andreeva (1968, 1976) listed as paratypes of B. karatauvi 17 ♀♀ collected together with the holotype and 8 ♀♀ collected in 1966–1967 in other regions of southern Tajikistan. As noted above, the type series comprises only 7 ♀♀ from Karatau Mts. All other females originally included in the type series are reidentified and considered here as belonging to other species of Anemesia .
SMNH |
Department of Paleozoology, Swedish Museum of Natural History |
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.
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Anemesia karatauvi ( Andreeva, 1968 )
Zonstein, Sergei 2018 |
Anemesia karatauvi
Marusik Y. M. & Zamani A. & Mirshamsi O. 2014: 3 |
Zonstein S. L. 2004: 352 |
Zonstein S. L. 2001: 11 |
Mikhailov K. G. 1997: 20 |
Mikhailov K. G. 1996: 77 |
Brachythele karatauvi
Zonstein S. L. 1987: 1013 |
Zonstein S. L. 1985: 159 |
Fet V. Y. 1984: 40 |
Brignoli P. M. 1983: 123 |
Andreeva E. M. 1976: 14 |
Brachythele karatauvi
Andreeva E. M. 1968: 70 |