Charmus laneus Karsch, 1879
publication ID |
https://doi.org/ 10.18590/euscorpius.2016.vol2016.iss220.1 |
DOI |
https://doi.org/10.5281/zenodo.7124485 |
persistent identifier |
https://treatment.plazi.org/id/B07187DF-A802-FF8D-FE8C-F9B69FB4FDB7 |
treatment provided by |
Felipe |
scientific name |
Charmus laneus Karsch, 1879 |
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Charmus laneus Karsch, 1879 View in CoL
( Figs. 12 View Figures 12–15 , 41–43 View Figures 39–46 , 47–83 View Figures 47–53 View Figures 54–59 View Figures 60–63 View Figures 64–65 View Figures 66–67 View Figures 68–70 View Figures 71–73 View Figures 74–79 View Figures 80–84 , 85–86 View Figures 85–87 , 96–98 View Figures 92–100 , 118–119 View Figures 107–119 , 194 View Figures 193–200 , 423–424 View Figures 403–429 , 548, Tables 1–2 View Table 1 View Table 2 )
Charmus laneus Karsch, 1879: 104–105 View in CoL ; Kraepelin, 1899: 39; Pocock, 1900: 32; Kraepelin, 1913: 131; Sreenivasa-Reddy, 1966: 253–254; Moritz & Fischer, 1980: 317; Kovařík, 1998: 108; Fet & Lowe, 2000: 123 (in part).
= Heterocharmus cinctipes Pocock, 1892: 47–48 , pl. IIIB, fig. 2, 2a–b (TL: India or Sri Lanka; BMNH). Syn. by Kraepelin, 1899: 39.
= Charmus minor Lourenço, 2002: 19–24 , figs. 1–14 (TL: Sri Lanka, Mannar District, Wilpattu National Park, 0.5 miles NE Cockmuttai; ZMUH). Syn. n.
TYPE LOCALITY AND TYPE REPOSITORY. Ceylon; ZMHB.
TYPE MATERIAL EXAMINED. Ceylon (now Sri Lanka), leg. Hoffmeister, 1♀ holotype ( Figs. 43 View Figures 39–46 , 80–82 View Figures 80–84 , 96–98 View Figures 92–100 ), ZMHB No. 3051 .
OTHER MATERIAL EXAMINED. Sri Lanka, North Central Province, Puttalam District, Eluwankulam , 08°12'35.1 "N 079°51'32"E, 52 m a.s.l. (Locality 15CN, Fig. 591 View Figures 590–591 ), 28.IV.2015, 1♂, FKCP, leg. Kovařík et al GoogleMaps .; North Central Province, Puttalam District, Eluwankulam , 08°17' 15"N 079°50'38.7"E, 38 m a.s.l. (Locality 15CO, Fig. 5 92 View Figures 5–11 View Figures 12–15 View Figures 16–19 View Figures 20–23 View Figures 24–29 View Figures 30–33 View Figures 34–38 View Figures 39–46 View Figures 47–53 View Figures 54–59 View Figures 60–63 View Figures 64–65 View Figures 66–67 View Figures 68–70 View Figures 71–73 View Figures 74–79 View Figures 80–84 View Figures 85–87 View Figures 88–91 View Figures 92–100 ), 28.IV.2015, 1♂ ( Figs. 41 View Figures 39–46 , 48–55 View Figures 47–53 View Figures 54–59 , 60, 62 View Figures 60–63 , 74–76 View Figures 74–79 , 1 18 View Figures 1–4 View Figures 5–11 View Figures 12–15 View Figures 16–19 , 194 View Figures 193–200 , 42 3 View Figures 39–46 , 548 View Figures 547–554 ) 1♀ ( Figs. 42 View Figures 39–46 , 58–59 View Figures 54–59 , 61, 63 View Figures 60–63 , 77–79 View Figures 74–79 , 8 3 View Figures 5–11 , 85 View Figures 85–87 , 119 View Figures 107–119 , 424 View Figures 403–429 ) 1juv. ( Figs. 56–57 View Figures 54–59 , 86 View Figures 85–87 ), FKCP, 2♂ ( Figs. 64–73 View Figures 64–65 View Figures 66–67 View Figures 68–70 View Figures 71–73 ) 1♀, UPSL, leg. Kovařík et al GoogleMaps .
DIAGNOSIS. Total length 14 mm (male) – 21.3 mm (female). Mesosoma, carapace, metasoma and telson of adults black; pedipalp femur almost entirely black with several small yellow spots; pedipalp patella yellowish with several black spots; legs yellow with black spots; chelicerae brown, with black reticulation. Carapace granular without carinae, anterior edge with epistome present medially. Tergites I–VI granular, obviously with one carina. Sternites without carinae. Metasomal segments IV–V or III–V punctate without developed carinae. Fifth metasomal segment length / width ratio 1.288–1.425 in female. Pectines with or without fulcra. Ratio of pedipalp chela length / fixed finger length in female 1.692–1.791. Movable and fixed fingers of pedipalps bearing 8 rows of granules, apical rows of 4–6 granules, and 3 terminal granules; each row of granules (except last) with one internal and two external accessory granules. Pectinal teeth number 16–18 in both sexes. Telson vesicle punctate, rather bulbous in male.
HEMISPERMATOPHORE ( Figs. 48–53 View Figures 47–53 ). Trunk very narrow, elongate, capsule region short ( Fig. 48 View Figures 47–53 ). Flagellum cylindriform, relatively short, robust, coiled. Median lobe broad, distally truncate, with straight dorsal carina near internal margin. Basal lobe well developed, a prominent, blunt, bilobate scoop arising dorsally near base of median lobe carina.
C HELICERA ( Figs. 66–67 View Figures 66–67 ). Manus with dark reticulated patterns on dorsal and ventral surfaces. Dorsal manus with 9 macrosetae near anterior margin. Movable finger with 2 dorsal macrosetae on anterior half. Ventrointernal aspect of manus and fixed finger with dense brush of microsetae, most if not all appearing fluorescent with intense terminal pinpoint fluorescence (i.e. putative chemoreceptive setae). Microsetae also present but sparse on ventral aspect of movable finger. Fingers with typical buthid dentition ( Vachon, 1963). Fixed finger with distal and subdistal denticles, and 2 basal denticles fused into bicusp. Dorsal margin of movable finger with 5 denticles: 1 large distal and 1 large medial, 1 smaller subdistal, and 2 small partially fused basal denticles. Ventral margin of movable finger with 3 denticles: 1 large distal and 2 smaller medial denticles. Ventral surface of fixed finger armed medially and basally with 2 small denticles concealed by dense brush of microsetae ( Fig. 67b View Figures 66–67 ).
COMMENTS. Lourenço did not study any specimens of C. laneus in spite of the fact that he cited six characters for distinguishing C. laneus from C. minor ( Lourenço, 2002: 23) . Several of these 'character differences' lie within the range of intraspecific variation (e.g. fulcra of pectines), and others are not valid. Lourenço stated that the movable finger of C. laneus bears 7–8 rows of granules, while that of C. minor bears 9 rows of granules. However, his own figure ( Lourenço, 2002: 18, fig. 1) shows that the male " paratype " of C. minor has only 8 rows of granules. Another problem is that according to the type material section ( Lourenço, 2002: 19) there exist only two types of C. minor – the male holotype and a juvenile (second instar) female paratype. Neither a male paratype, nor an adult female paratype were listed. Thus, it is surprising that Lourenço claimed that the female of C. minor has a differently flattened sternum than the male ( Lourenço, 2002: 23). If this was a reference to the second instar juvenile female paratype, the diagnostic character needs to specified for adult females. Under "Ecological observations" Lourenço (2002: 23) wrote that "The specimens of C. laneus studied by Vachon (1982) were all collected in the central-south region of Sri Lanka which is characterised by high altitudes reaching to more than 1000 m ...". In fact, the three specimens studied by Vachon (1982: 81) were collected at altitudes of 250 m, 600 m, and 1350 m a.s.l. and according to Vachon’s opinion they all belong to the same species, ' C. laneus '. Neither Vachon (1982) nor Lourenço (2002) studied the holotype of C. laneus , and as we show here, these three Charmus specimens from central Sri Lanka actually belong to a different species. These three specimens are herein designated as types of C. saradieli sp. n., and C. minor Lourenço, 2002 is synonymized with C. laneus Karsch, 1879 as there are no significant differences between them at the species level.
DISTRIBUTION. Sri Lanka.
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Charmus laneus Karsch, 1879
Kovařík, František, Lowe, Graeme, Ranawana, Kithsiri B., Hoferek, David & Š, V. A. 2016 |
Charmus minor Lourenço, 2002: 19–24
LOURENCO, W. R. 2002: 24 |
Heterocharmus cinctipes
KRAEPELIN 1899: 39 |
POCOCK, R. I. 1892: 48 |
Charmus laneus
FET, V. & W. D. SISSOM & G. LOWE & M. E. BRAUNWALDER 2000: 123 |
KOVARIK 1998: 108 |
MORITZ, M. & S. - CH. FISCHER 1980: 317 |
SREENIVASA-REDDY, R. P. 1966: 253 |
KRAEPELIN 1913: 131 |
POCOCK, R. I. 1900: 32 |
KRAEPELIN 1899: 39 |
KARSCH 1879: 105 |