Reddyanus jayarathnei Kovařík, 2016
publication ID |
https://doi.org/ 10.18590/euscorpius.2016.vol2016.iss220.1 |
publication LSID |
lsid:zoobank.org:pub:DD0DF45D-F63A-4AA2-8EFF-03CF99E297EF |
DOI |
https://doi.org/10.5281/zenodo.7124553 |
persistent identifier |
https://treatment.plazi.org/id/FE1515A9-8302-46D4-8298-11BFB4555882 |
taxon LSID |
lsid:zoobank.org:act:FE1515A9-8302-46D4-8298-11BFB4555882 |
treatment provided by |
Felipe |
scientific name |
Reddyanus jayarathnei Kovařík |
status |
sp. nov. |
Reddyanus jayarathnei Kovařík View in CoL , sp. n.
( Figs. 14 View Figures 12–15 , 206 View Figures 201–208 , 215–216 View Figures 209–224 , 231–232 View Figures 225–240 , 248, 257 View Figures 241–259 , 334–357 View Figures 334–337 View Figures 338–348 View Figures 349–354 View Figures 355–357 , 415–416 View Figures 403–429 , 569, Tables 4–5 View Table 4 View Table 5 )
http://www.zoobank.org/urn:lsid:zoobank.org:act:F E1515A9-8302-46D4-8298-11BFB4555882
TYPE LOCALITY AND TYPE REPOSITORY. Sri Lanka, Galle district GoogleMaps , Kanneliya Rain Forest, 06°15'04" N 80°20'18" E; UPSL.
TYPE MATERIAL. Sri Lanka, Galle District , Kanneliya Rain Forest, 06°15'04" N 80°20'18" E ( Fig. 357 View Figures 355–357 ), 1♂ (holotype, Fig. 356 View Figures 355–357 ) GoogleMaps 1♀ (paratype, Fig. 355 View Figures 355–357 ), UPSL GoogleMaps , 1♂ (paratype, Figs. 206 View Figures 201–208 , 215 View Figures 209–224 , 231 View Figures 225–240 , 248, 257 View Figures 241–259 , 334–335 View Figures 334–337 , 338, 340, 343–351 View Figures 338–348 View Figures 349–354 , 415 View Figures 403–429 , 569) 1♀ (paratype, Figs. 216 View Figures 209–224 , 232 View Figures 225–240 , 336–337 View Figures 334–337 , 339, 341–342 View Figures 338–348 , 352–354 View Figures 349–354 , 416 View Figures 403–429 ), FKCP, V.– XI.2015, leg. S. Jayarathne.
ETYMOLOGY. Named after V. A. Sanjeewa Jayarathne who collected the types.
DIAGNOSIS. Total length 37.1 mm (female) – 45.5 mm (male). Male with slightly longer metasomal segments and telson than female. Pedipalp segments approximately the same length and width in both sexes. Pedipalp movable finger longer than manus of chela in both sexes. Pedipalps and legs with brown maculation, identical on femur and patella. First metasomal segment bears 10 carinae, second through fourth segments bear eight carinae, fifth segment bears five carinae in female and three to five in male. Posterior terminal tubercle of each dorsal carina on metasomal segments of both sexes scarcely larger than preceding tubercles. Subaculear tooth wide and rounded, dorsally with granules in four rows; six symmetrical granules in three rows and one or two granules on tip. Ratio of metasomal segment II length/ width 1.81 in male. Glabrous zone on posterior part of fifth sternite present medially in male. Pectinal teeth number 12 in female, 14 in male.
DESCRIPTION. Total length 37.1 mm (female paratype) – 45.5 mm (male holotype). The habitus is shown in Figs. 334–337 View Figures 334–337 . For measurements and ratios see Tables 4–5 View Table 4 View Table 5 . For position and distribution of trichobothria of pedipalps see Figs. 344–348 View Figures 338–348 . The male has slightly longer metasomal segments and telson than the female ( Figs. 349– 354 View Figures 349–354 ).
Coloration ( Figs. 334–337 View Figures 334–337 ). Entire mesosoma and carapace dark, almost black with yellow to reddish spots. Chelicera strongly reticulated, with spotted fingers. Pedipalps dorsally and laterally reddish, with brown to black spots, identical on femur and patella. Pedipalp chela fingers reddish black. Legs with same color and pattern as pedipalp femur and patella. Metasomal segments reddish brown with the spots. Telson reddish brown with spots.
Mesosoma and carapace ( Figs. 338–341 View Figures 338–348 ). Carapace without carinae but with large granules. Mesosoma with one granulated median carina. Tergite VII pentacarinate. Fifth sternite with glabrous zone on posterior medial part in the male. Seventh sternite with four incomplete carinae, sparsely granulate. Pectinal tooth count is 12 in the female, 14 in the male. Pectines with three marginal lamellae and seven middle lamellae. The lamellae bear numerous pale setae.
Metasoma and telson ( Figs. 215–216 View Figures 209–224 , 349–354 View Figures 349–354 , 415– 416 View Figures 403–429 ). The first metasomal segment bears 10 carinae and the second to the fourth segments bear eight carinae, the fifth segment bears five carinae well developed in the female and only indicated or absent in the male. Lateral inframedian carinae may be indicated on second metasomal segment. Ventral carina present on telson. Intercarinal surfaces of metasoma granulated including dorsal surface mainly in the female. In both sexes, posterior terminal tubercle of each dorsal carina on metasomal segments not enlarged. Telson elongate, with subaculear tooth wide and rounded, dorsally with granules in four rows; six symmetrical granules in three rows and one or two granules on the tip.
Pedipalps ( Figs. 231–232 View Figures 225–240 , 342–348 View Figures 338–348 ). Femur and patella only very sparsely hirsute, with complete carinae, granulated. Dorsal carinae indicated on chela manus in both sexes. Sixth row of granules on movable finger with one external granule. The seventh row of granules on the fixed finger without additional granules.
Legs ( Fig. 206 View Figures 201–208 ). Femur and patella bear complete carinae and are granulated. Legs hirsute without bristle combs.
AFFINITIES. The described features distinguish R. jayarathnei sp. n. from all other species of the genus. R. jayarathnei sp. n. is well characterized by the glabrous zone on the posterior medial part of the fifth sternite in the male, which is not as extensive in R. ranawanai sp. n. ( Fig. 570 View Figures 555–570 versus Fig. 569 View Figures 555–570 ) and is absent in other Sri Lankan Reddyanus species ( Figs. 567–568 View Figures 555–570 ).
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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