Karaops banyjima Crews, 2013
publication ID |
https://dx.doi.org/10.3897/zookeys.1150.93760 |
publication LSID |
lsid:zoobank.org:pub:A38C5FB6-9F66-4F85-8788-AAA53D21704D |
persistent identifier |
https://treatment.plazi.org/id/C36072AB-5A8A-5854-B3D3-CCC4BE627764 |
treatment provided by |
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scientific name |
Karaops banyjima Crews, 2013 |
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Karaops banyjima Crews, 2013 View in CoL
Figs 64B View Figure 64 , 65C-F View Figure 65 , 66B, E View Figure 66 , 67A View Figure 67 , 68A, C, E, F View Figure 68 , Maps 1 View Map 1 , 9A, B View Map 9
Karaops banyjima Crews, 2013: 466, figs 33, 34 (♀, examined).
Material examined.
Western Australia • 1♂, 1 imm.; ~ 1.5 km from Hamersley Gorge , on side of road; 22°14'5.86"S, 117°58'8.46"E; ~ 571 m; 13 May 2016; S. Crews, J. DeJong leg.; under rocks in dry creek bed; sel_1173-1174; SCC16_029; (WAM T155549, 155550) GoogleMaps • 1♂ (reared in captivity), 7 imm.; Karijini National Park, Dale’s Gorge, along trail to Circular Pool by Fortescue Falls sign at bottom of trail to gorge; 22°28'41.18"S, 118°33'43.55"E; ~ 594 m; 14 May 2016; S. Crews, J. DeJong leg.; under rocks, abundant; sel_1183-1190; SCC16_031; (WAM T155559-155566) GoogleMaps • 8 imm.; Great Northern Highway ( Newman-Port Hedland Road ); 23°9'6.73"S, 119°19'46.11"E; ~ 702 m; 15 May 2016; S. Crews, J. DeJong leg.; under rocks on side of road; sel_1198-1205; SCC16_034; (WAM T155574-155581) GoogleMaps .
New records.
Western Australia • 1♂; Yandi (Marillana Creek), ~ 98 km NW of Newman; 22°43'22.2"S, 118°58'30.2"E; 8 Sep. 2014; S. Callan, C. Brooks leg.; foraging; under rocks; (WAM T134063) • 1 imm.; Yandi (Marillana Creek), ~ 98 km NW. of Newman; 22°44'46.1"S, 119°00'30.1"E; 8 Sep. 2014; S. Callan, C. Brooks leg.; foraging; under rocks; (WAM T134072) • 1 imm.; Yandi (Marillana Creek), ~ 98 km NW of Newman; 22°43'33.23"S, 118°59'02.47"E; 14 May 2013; S. Callan leg.; foraging; drainage/ridge-outcrop; (WAM T130404) • 1 imm.; Yandi (Marillana Ck), ~ 98 km NW of Newman; 22°42'39.70"S, 119°00'50.36"E; 14 May 2013; S. Callan, Biologic Env. leg.; foraging; ridge-outcrop; (WAM T130400) • 1 imm.; Yandi (Marillana Ck), ~ 98 km NW of Newman; 22°42'33.08"S, 119°00'15.33"E; 14 May 2013; S. Callan, Biologic Env. leg.; foraging; ridge-outcrop/veg. grove; (WAM T130402) • 1 imm.; Yandi (Marillana Creek), ~ 98 km NW of Newman; 22°42'33.08"S, 119°00'15.33"E; 14 May 2013; S. Callan, Biologic Env. leg. foraging; ridge-outcrop/ veg. grove; (WAM T130403) • 1 imm.; Yandi (Marillana Ck), ~ 98 km NW of Newman; 22°44'23.42"S, 119°00'13.28"E; 14 May 2013; S. Callan, Biologic Env. leg.; foraging; drainage/ridge-outcrop; (WAM T130405) • 1 imm.; Yandi (Marillana Ck), ~ 98 km NW of Newman; 22°46'27.87"S, 119°07'43.67"E; 14 May 2013; S. Callan, Biologic Env. leg.; foraging; ridge-outcrop/ gully; (WAM T130406) • 1 imm.; Yandi (Marillana Ck), ~ 98 km NW of Newman; 22°46'27.87"S, 119°07'43.67"E; 14 May 2013; S. Callan, Biologic Env., leg.; foraging; ridge-outcrop/gully; (WAM T130407) • 1 imm.; Yandi (Marillana Ck), ~ 98 km NW of Newman; 22°46'28.48"S, 119°07'24.24"E; 14 May 2013; S. Callan, Biologic Env., leg.; foraging; ridge-outcrop/gully; (WAM T130409) • 1 imm.; Yandi (Marillana Ck), ~ 98 km NW of Newman; 22°46'33.74"S, 119°07'16.60"E; 14 May 2013; S. Callan, Biologic Env. leg.; foraging; ridge-outcrop/gully; (WAM T130410) • 1 imm.; Yandi (Marillana Ck), ~ 98 km NW of Newman; 22°43'49.65"S, 119°02'49.81"E; 14 May 2013; S. Callan, Biologic Env. leg.; foraging; gully/minor outcrop; (WAM T130411) • 1 imm.; Yandi (Marillana Ck), ~ 98 km NW of Newman; 22°43'49.65"S, 119°02'49.81"E; 14 May 2013; S. Callan, Biologic Env. leg.; foraging; gully/minor outcrop; (WAM T130412) • 1 imm.; Yandi (Marillana Ck), ~ 98 km NW of Newman; 22°43'55.81"S, 119°03'00.10"E; 14 May 2013; S. Callan, Biologic Env. leg.; foraging; drainage/ridge-outcrop; (WAM T130413) • 1 imm.; Yandi (Marillana Ck), ~ 98 km NW of Newman; 22°44'29.32"S, 118°59'34.47"E; 14 May 2013; S. Callan, Biologic Env. leg.; foraging; ridge-outcrop/drainage; (WAM T130415) • 1 imm.; Yandi (Marillana Ck), ~ 98 km NW of Newman; 22°42'50.61"S, 119°01'13.15"E; 14 May 2013; S. Callan, Biologic Env. leg.; foraging; ridge-outcrop; (WAM T130416) • 1♀; Area C, 87.3 km NW of Newman; 22°53'43"S, 119°02'42"E; 17 Feb. 2010; M. Greenham leg.; gully, in soil; (WAM T101159) • 1♀; Karijini National Park, Dales Gorge; 22°28'41"S, 118°33'44"E; 12 Mar. 2015; M.S. Harvey leg.; under rock; (WAM T135465) • 1♀; Karijini National Park, Dales Gorge; 22°28'41"S, 118°33'44"E; 15 Mar. 2015; M.S. Harvey et al. leg.; under rock; (WAM T135466).
Diagnosis.
The female (Fig. 66E View Figure 66 ) is somewhat similar to Karaops burbidgei by the location of the copulatory openings and the general shape of the structures of the endogyne ( Crews and Harvey 2011: figs 37, 38). In K. banyjima , however, the copulatory openings are located in a depression that is m-shaped along the top margin and w-shaped along the bottom margin ( Crews 2013: fig. 33), the ducts connecting the spermathecae and the accessory bulbs are not twisted, and the spermathecae and accessory bulbs are highly sclerotized ( Crews 2013: fig. 34).
The male is most similar to Karaops nyangumarta , but the two species can be differentiated by the tegular lobe, the median apophysis, the conductor, and the dRTA. In K. banyjima , the narrowing of the tegular lobe to the embolus is nearly midway from the basal and distal portions of the bulb (Fig. 69A, B View Figure 69 ). In K. nyangumarta , this point is in the basal third of the bulb (Fig. 63C View Figure 63 ). The median apophysis of K. banyjima has no spinules (Fig. 69A, B View Figure 69 ), and the median apophysis of K. nyangumarta has a dense array of spinules (Fig. 63C View Figure 63 ). The conductor of K. banyjima does not reach the retrolateral edge of the bulb, and the tip is directed laterally (Fig. 69A, B View Figure 69 ), whereas in K. nyangumarta , the conductor reaches the retrolateral side of the bulb, and the tip of the conductor is directed ventrally (Fig. 63C View Figure 63 ). The dRTA of K. banyjima is rather short and stout (but not like a little teapot) (Fig. 69A, B View Figure 69 ), whereas that of K. nyangumarta is longer, narrower, and curved slightly ventrally (Fig. 63C, D View Figure 63 ). It is somewhat difficult to distinguish the two in life by the abdominal pattern, but K. nyangumarta males have more mottling dorsally on the abdomen.
Description.
Male (sel_1174, WAM T155550). Total length 4.77. Carapace: length 2.56, width 3.16. Chelicerae: promargin with three teeth, the two closest to the fang are very close together, smallest closest to fang, other two larger, same retromargin with two teeth (1-0-1). Eyes: AER nearly recurved; PER strongly recurved; diameters AME 0.19, ALE 0.12, PME 0.23, PLE 0.37; interdistances AME-PME 0.04, PME-ALE 0.13, ALE-PLE 0.20, ALE-ALE 1.33, AME-AME 0.44, PLE-PLE 1.6. Sternum: length 1.24, width 1.67. Abdomen: length 2.21, width 2.10. Color (in life Figs 67A, B View Figure 67 , 68A View Figure 68 , 70A View Figure 70 /preserved Figs 64B, D View Figure 64 , 65F View Figure 65 , 66B View Figure 66 ): Carapace: dusky markings on tan background, in nature, pale yellowish brown with darker markings, orange around eye area/markings mostly faded, still visible laterally and just behind eyes, yellowish white. Chelicerae: yellowish white with a small spot below clypeus, paturon with curved, dark mark frontally (Fig. 66B View Figure 66 ), with more setae anteriorly than laterally, especially inner margin. Maxillae: whitish. Labium: dusky, pale distally. Sternum: yellowish white. Abdomen: dorsally setose, dark tan to brown, paler medially until posterior third, anteriorly with pale spot on either side of paler median area, dark horizontal band near posterior of abdomen, posterior of dark band with pale setae making somewhat w-shaped mark; in nature, at least in juveniles, anterior pale spots and w-shaped mark are easily discernable (Fig. 68A View Figure 68 )/most paler areas very pale to white, darker areas very dark, with no particular pattern or shape visible, orangish setae around margin; ventrally yellowish white. Spinnerets: with dusky markings. Legs: pale yellowish to tan, dusky ventrally, Cx, Tr with dark prolateral spot, Fm with marks that do not encircle the legs, unpigmented centrally, Pt with dark annulation basally, Ti with two annulations, one basal and the other distal though not at joint with Mt, Mt with two annulations, one basal, one distal, Ta tip dark/markings quite faded; juveniles with Fm setal tufts of flat, white setae; spination leg I Fm d 1-1-1, pl 1-1-1, rl 0-0-1, Ti v 2-2-2-2-2, rl 1-1, pr 1-1, Mt v 2-2-2-2; leg II Fm d 1-1-1, pr 0-0-1, rl 0-0-1, Ti v 2-2-2-2-2-2, pr 0-1, rl 0-1, Mt v 2-2-2-2, pr 0-1-0; leg III Fm d 1-1-1, pr 0-0-1, rl 0-1-1, Ti v 2-2, Mt v 2-2; leg IV Fm d 1-1-1, pr 0-1-1, rl 0-1-1, Ti v 2-2, pr 1-1, rl 1-1, Mt v 2-1; leg formula 3421; measurements leg I 11.10 (3.08, 1.33, 3.10, 2.22, 1.37); leg II 12.43 (3.26, 1.47, 3.55, 2.69, 1.46); leg III 14.23 (3.81, 1.18, 3.80, 3.40, 2.04); leg IV 12.54 (3.76, 1.08, 3.19, 3.02, 1.49). Palp: spination Fm d 0-1-2; 2.60 (0.63, 0.46, 0.51, 1.00); Ti dark dorsally, with marking extended to both pro- and retrolateral sides, basal half of Cy with dark marks dorsally (Figs 64D View Figure 64 , 65D, E View Figure 65 , 69A-C View Figure 69 ) both vRTA and dRTA short, striae present on dRTA; rbcp large; Cy round triangular, extended retrobasally (Fig. 69C View Figure 69 ); C large but mostly restricted to medioapical part of bulb, TS covering part of C, CS covering ~ 1/2 of E, medially unsclerotized, sclerotized more distally, tip very sclerotized, ventrally projecting arch at point where unsclerotized area comes into contact with more sclerotized area, sclerotized projection directed retrolaterally, narrowed to flattened, pointed tip directed ventrally, groove along extended distal part; E short, arising from very large TL at ~ 9 o’clock, hooked, ending at ~ 1 o’clock; MA broad throughout, only slightly narrowing distally, not very sclerotized, distal portion gently curled.
Female. The description of the female can be found in Crews (2013).
Variation.
Additional males were measured and size ranges from 4.01-4.77. Specimen sel_1187 was smaller overall, with smaller features in general and also darker than sel_1174.
Distribution.
Known from only the Hamersley subregion of the Pilbara, Western Australia (Fig. 68C, E, F View Figure 68 , Map 9A, B View Map 9 ).
Natural history.
Males have matured in captivity and in nature in September and October, a dry time, transitioning from cool to hot. Females have been collected in February and March, a hot, wet time of the year (Suppl. material 2: tables S1, S21).
Discussion.
The palps of sel_1198 (WAM T155574) were stuck in the exuvia when molting, but the species could be determined by the RTA and molecular data (Fig. 65C-E View Figure 65 ). The distribution overlaps that of Karaops nyangumarta , is close to that of K. martamarta , and perhaps overlaps with K. morganoconnelli sp. nov. However, none of the different species examined are known to have ever been taken from the same place at the same time.
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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Karaops banyjima Crews, 2013
Crews, Sarah C. 2023 |
Karaops banyjima
Crews 2013 |