Chaerilus kautti, Kovařík & Lowe & Stockmann & Šťáhlavský, 2020
publication ID |
https://doi.org/ 10.5281/zenodo.4648882 |
publication LSID |
lsid:zoobank.org:pub:DB1216AA-360D-4FC6-BA4C-13D3B032B359 |
DOI |
https://doi.org/10.5281/zenodo.4773482 |
persistent identifier |
https://treatment.plazi.org/id/8275997C-69A8-4494-A6F1-ED502A69E1FF |
taxon LSID |
lsid:zoobank.org:act:8275997C-69A8-4494-A6F1-ED502A69E1FF |
treatment provided by |
Carolina |
scientific name |
Chaerilus kautti |
status |
sp. nov. |
Chaerilus kautti View in CoL sp. n.
( Figures 1–50 View Figures 1–2 View Figures 3–6 View Figures 7–14 View Figures 15–22 View Figures 23–32 View Figures 33–41 View Figures 42–43 View Figures 44–48 View Figures 49–50 , 84 View Figures 84–86 , Table 1 View Table 1 )
http://zoobank.org/urn:lsid:zoobank.org:act:8275997C- 69A8-4494-A6F1-ED502A69E1FF
TYPE LOCALITY AND TYPE REPOSITORY. Thailand, Prachuap Khiri Khan Province, Khao Ma Rong Cave , 11.2021900°N 99.4946250°E, 56 m a. s. l. GoogleMaps , FKCP.
TYPE MATERIAL ( FKCP). Thailand, Prachuap Khiri Khan Province, Khao Ma Rong Cave , 11.2021900°N 99.4946250°E, 56 m a. s. l. ( Fig. 48 View Figures 44–48 ), 19.VIII.2018, 1♂ (holotYpe, 1770, Figs. 1 View Figures 1–2 , 3–4 View Figures 3–6 , 7–8 View Figures 7–14 , 15, 20–32 View Figures 15–22 View Figures 23–32 , 44–47 View Figures 44–48 ), leg. Peter Kautt, GoogleMaps 1♀ (paratYpe, Figs. 2 View Figures 1–2 , 5–6 View Figures 3–6 , 9–14 View Figures 7–14 , 16–19 View Figures 15–22 , 33– 43 View Figures 33–41 View Figures 42–43 , 49–50 View Figures 49–50 , scorpion born 27.IX.2020), leg. Britta & Mark Stockmann, 16 juvs. (paratYpes, Figs. 49–50 View Figures 49–50 , offspring of the female paratYpe 27.IX.2020, still alive), bred bY F. Kovařík and M. Stockmann GoogleMaps .
ETYMOLOGY. The specific epithet is a patronYm honoring Peter Kautt, the collector of the male holotYpe of the new species.
DIAGNOSIS (♂ ♀). Total length 37–43 mm; two pairs of lateral eYes and one pair of median eYes; ventral surface of cheliceral fixed finger with 4 denticles; male differs from female in having pedipalp chela much narrower; chela length/width ratio ♂ 4.55, ♀ 2.88; movable finger of pedipalp with 11 imbricated rows of granules; fingers straight in both sexes; pedipalp chela with 7–8 carinae; pectinal tooth count ♂ 6, ♀ 4; carapace granulated sparselY in male, denselY in female; mesosomal tergites granulated, mainlY in the female; all sternites smooth without carinae and granules; metasoma I–III with 6 or 8 carinae, ventral carinae maY be absent.
DESCRIPTION. Total length ♂ 37 mm, ♀ 43 mm; color reddish orange to brown, maculose; chelicerae ( Figs. 42–43 View Figures 42–43 ) sparselY granulated dorsallY, Yellow and stronglY reticulate, anteriorlY black; male differs from female in having pedipalp chela much narrower with short fingers; chela length/width ratio ♂ 4.55, ♀ 2.88; male with larger pectines ( Figs. 8 and 10 View Figures 7–14 ); no sexual dimorphism in shape of metasoma and telson; trichobothrial pattern as shown in Figs. 23–29 View Figures 23–32 , measurements in Table 1 View Table 1 .
Carapace and mesosoma ( Figs. 7–10 View Figures 7–14 ). Carapace covered bY large granules in female, almost smooth in male; anterior margin of carapace weaklY concave; two well developed pairs of lateral eYes and one pair of median eYes present; mesosomal tergites irregularlY granulated in female, almost smooth in male; all sternites smooth without carinae and granulation; sternite V with smooth patch present; pectinal tooth count ♂ 6, ♀ 4.
Metasoma and telson ( Figs. 15–22 View Figures 15–22 ). Metasoma I–II with 6 or 8 incomplete carinae, ventral carinae reduced or absent; metasoma IV with 8 carinae, metasoma V with 5 carinae; all carinae composed of sparse, large granules; intercarinal surfaces sparselY, irregularlY granulated, more so on lateral surfaces of all segments, and ventral surfaces of segment V; metasomal segments I–III ventrallY smooth; all segments verY sparselY hirsute; telson elongate, ampullate, smooth, verY sparselY hirsute.
Pedipalps ( Figs. 23–41 View Figures 23–32 View Figures 33–41 ). Pedipalp chela elongated in male, rather stout in female; movable finger with 11 and fixed finger with 10 imbricated rows of granules; chela with 7 or 8 carinae, smooth in male, partlY finelY granulated in female; carina on dorsoexternal surface of the manus maY be incomplete; dorsal and internal surfaces of chela with reticulate granulation patterns; patella with 5–6 smooth carinae, surfaces of patella smooth except internal surface which is finelY granulated; femur denselY granulated with 4 carinae.
Legs ( Figs. 11–14 View Figures 7–14 ). Hirsute, without bristlecombs and carinae; femora and patellae granulated dorsallY, other surfaces smooth; tarsomeres with 4 rows of spiniform setae; spiniform seta formula of inner rows 6–7/7–8: 7–8/6–7: 7–8/8–9: 6–8/8–9; of outer rows 3–4/3–4 on all legs.
Hemispermatophore ( Figs. 44–47 View Figures 44–48 ). Fusiform; distal lamina short, broad, weaklY tapered, apex rounded; capsule with distal carina weaklY sclerotized; sperm hemiduct delineated bY two thin, sclerotized carinae, of which the distal is longer, the basal shorter; trunk long, as broad as capsule. Measurements of right hemispermatophore (mm): distal lamina length 0.64, capsule length 0.72, trunk length 1.96, pedicel length 0.42, capsule width 0.63. Left hemispermatophore with shorter trunk, length 1.70.
Karyotype ( Fig. 84 View Figures 84–86 ). Male holotYpe was analYzed. During metaphase I 59 bivalents were observed ( Fig. 84 View Figures 84–86 ), implYing that 2n=118. Chiasmata were not observed during meiosis.
AFFINITIES. Chaerilus kautti sp. n. is reliablY distinguished from all other Chaerilus species bY the following unique combination of two characters: movable pedipalp finger with 11 imbricated granule rows; and pedipalp chela length/width ratio 4.55 in the male.
A movable pedipalp finger with 11 (or 10–11) imbricated granule rows is also found in six other species of the genus ( C. cimrmani Kovařík, 2012 from Thailand, C. hofereki Kovařík, 2014 from Vietnam, C. julietteae Lourenço, 2011 from Vietnam, C. neradorum Kovařík et al., 2018 from Thailand, C. robinsoni Hirst, 1911 from MalaYsia and Indonesia, and C. stockmannorum Kovařík et al., 2018 from Thailand). However, males of all of these species have a pedipalp chela length/width ratio between 1.84 ( C. hofereki ) and 3.13 ( C. julietteae ).
COMMENTS ON LOCALITIES AND LIFE STRATEGY. The tYpe localitY is located on an isolated karst mountain close to the eastern coast of Thailand, west of Bang Saphan. The entire mountain is clothed in primarY forest, but is surrounded bY cultivated farmland with mostlY oil palms and gumtrees. The tYpe localitY is close to two extensive caves, but C. kautti sp. n. does not appear to be associated with them. Climate conditions are warm and verY wet during the wet season from MaY to November, and slightlY cooler and drier during the drY season from December to April. Even during the drY season, the area is verY humid and water is alwaYs present.
The male from 2018 was collected during heavY rain on a dark night, the female from 2019 on a drY night without wind during a new moon. The average temperatures on both nights were ca. 25–26°C with verY high humiditY.
Both specimens were found at night on the ground, between leaf litter or sitting openlY on rocks. In captivitY, the scorpions concealed themselves under bark or in moss. The probablY do not excavate burrows, but instead shelter between rocks, or in wood and leaf litter in their habitat.
Other scorpions observed in this habitat were Heterometrus cimrmani Kovařík, 2004 , Lychas scutilus Koch 1845 , and Liocheles australasiae Fabricius, 1775 .
An adult gravid female collected in 2019 gave birth in captivitY to 48 juveniles after 11 months.
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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