Appearances often deceive in racerunners: integrative approach reveals two new species of Eremias (Squamata: Lacertidae) from Pakistan Masroor, Rafaqat Khan, Muazzam Ali Nadeem, Muhammad Sajid Amir, Shabir Ali Khisroon, Muhammad Jablonski, Daniel Zootaxa 2022 2022-08-15 5175 1 55 87 Masroor & Khan & Nadeem & Amir & Khisroon & Jablonski, 2022 Masroor & Khan & Nadeem & Amir & Khisroon & Jablonski 2022 [151,327,654,681] Reptilia Lacertidae Eremias Animalia Squamata 15 70 Chordata species rafiqi sp. nov.  Suggested vernacular name: Rafiq’s Racerunner Pashto name:     Holotype. PMNH 856(cyt b: n/a; Rag1: n/a), an adult male, collected from Tanishpa village, Torghar Mountains, Killa Saifullah district, Balochistan( 31.1869º N, 68.4126º E; Fig. 1), elevation 2,506 ma. s. l.,  May 25, 1997, leg. Khalid Javed Baig( Fig. 4).   FIGURE 4.The holotype of  Eremias( Aspidorhinus) rafiqi  sp. nov.(PMNH 856) from Tanishpa village, Torghar Mountains, Killa Saifullah district, Balochistan, Pakistan.   Paratypes. Males:  PMNH 855(cyt b: n/a; Rag1: n/a), 857 (cyt b: n/a; Rag1: n/a),  PMNH 859(cyt b: n/a; Rag1: n/a),  PMNH 861(cyt b: n/a; Rag1: n/a),  PMNH 4056(cyt b: n/a; Rag1:  MT554487).  Females :  PMNH 3724(cyt b: n/a; Rag1:  MT554476),  PMNH 3735(cyt b:  MT554461; Rag1:  MT554477),  PMNH 4058(cyt b: n/a; Rag1: n/a).  Juveniles :  PMNH 837(cyt b: n/a; Rag1: n/a),  PMNH 3723(cyt b:  MT554470; Rag1:  MT554496),  PMNH 4053(cyt b:  MT554457; Rag1:  MT554485),  PMNH 4054(cyt b:  MT554454; Rag1:  MT554480).  PMNH 857, collected along with the holotype;  PMNH 855and 861,  May 26, 1997, Ashewat, Qamar Din Karez, Zhob district( 31.3448ºN, 68.6307ºE), leg. Khalid Javed Baig;  PMNH 859,  May 24,1997, Tanishpa village, Torghar, Killa Saifullah district, leg. Khalid Javed Baig;  PMNH 3723–24,  October 09, 2017, Khar, Nushki district, Balochistan( 29.5879ºN, 65.6609ºE), leg. Muazzam Ali Khan;  PMNH 3735,  October 21, 2017, Khar, Nushki district, leg. Muazzam Ali Khan;  PMNH 4053,  September 05, 2018, Zamkai Nala, Tanishpa village, Torghar, Killa Saifullah district( 31.1930ºN, 68.4111ºE), leg. Rafaqat Masroor;  PMNH 4054,  September 01, 2018, Ashewat, Qamar Din Karez, Zhob district, leg. Rafaqat Masroor;  PMNH 4056and 4058,  August 30, 2018, Kunder, Torghar, Killa Saifullah district, leg. Ibad ur Rehman( Figs. 5& 6).   FIGURE 5.The dorsal and ventral views of selected paratypes of  Eremias( Aspidorhinus) rafiqi  sp. nov.and  E. ( Aspidorhinus) killasaifullahi  sp. nov.from Pakistan at different age stages.  Morphological diagnosis.A large-sized lacertid lizard, maximum snout-vent length ( SVL) = 99.3 mm, tail 1.67 to 1.89 times longer than body length ( SVL), hindlimbs relatively long ( HLL/ SVLratio 0.6–0.8); subocular scale reaching to the edge of the mouth, 5–7 (mainly 6, rarely 5) anterior to subocular; dorsals 56–67; ventrals in 14–17 oblique longitudinal series; frontal separated from supraoculars; the height of the first two to three transverse rows of ventral scales in the pectoral region more than its breadth; 17–21 femoral pores on each side, separated medially by 1–4 scales (mainly 3, rarely 1), the space between the femoral pores less than one–fourth length of each row; toes without fringe, encircled by three scales in a single series of 22–27 unicarinate and bicarinate scales underneath; the tip of the fourth toe reaches to the forelimb and extends to just behind the collar. The adult specimens are grayish in life with four series of longitudinal black ocelli on the dorsum originating from behind the parietals and extending onto the tail; on each lateral side, a broader dark stripe originates from behind the eye and continues onto the tail with disconnected white round ocelli at the margins as well as white ocelli inside the stripe.   FIGURE 6.The variation of dorsal body color and pattern in different age stages of the newly described species,  Eremias( Aspidorhinus) rafiqi  sp. nov.and  E. ( Aspidorhinus) killasaifullahi  sp. nov.  Molecular data.  Eremias rafiqi  sp. nov.represents the so-called Zabol clade sensu Rastegar-Pouyani et al.(2010)from eastern Iranand the clade E identified by Khan et al.(2021)from northeastern Balochistan, Pakistan. Whereas Rastegar-Pouyani et al. (2010)identified this clade solely on mtDNA (cyt b, 12S), Khan et al.(2021)used mitochondrial (16S, COI, cyt b) as well as nuclear data (Rag 1) that clearly showed deep differentiation of this new species from other available sequences of the genus. The distinction of  Eremias rafiqi  sp. nov.is supported by its phylogenetic position (monophyletic clade among other species of  E. persicacomplex, sister to  E. fahimiibut with weak statistical support; Fig. 1), the differentiation on solely Rag1 dataset ( Fig. 2), and the value of the uncorrected pdistances reaching from 8.5% (  E. fahimii) to 20.7% (  E. strauchi) ( Table 3). The intraclade genetic diversity (cyt b) is 2 % with six detected haplotypes found in Iranand Pakistan( Fig. 2, Table 3).   Etymology. The species epithet “  rafiqi” is taken from the first name of late Rafique Ahmed Rajput (1968– 2008) to whom the new species is dedicated. The deceased Rajput served in SindhWildlife Department from 1986 till his demise. With no formal education in wildlife research, conservation and management, his passion for the conservation of wildlife in Pakistanremain unparalleled. From collecting the first-ever data of  Ursus arctos isabellinusin the high-altitude Deosai Plateau, Gilgit-Baltistan, to the faunistic studies in the Indus River Delta and desert areas, he was a symbol of hard work. He also has very sound techniques for the collection of lizards and snakes. Unfortunately, during one such endeavor for gathering faunistic data, he collected a juvenile venomous krait,  Bungarussp.(possibly  B. persicus) from Jiwani town, Gwadar District, Balochistanand mistaken its identity with non-venomous  Lycodonspecies.On the morning of October 13, 2008, when he was shifting the live snake from a container to permanently preserve it for research purposes, the snake bit him multiple times.After a couple of hours, Rajput felt severe pain, anxiety and dizziness. He was immediately taken to the hospital in Karachi, where the doctors told his relatives that anti-snake venom is not available and asked them to get it from the pharmacy market. By the time the anti-venom was arranged, Rajput breathed his last.   Description of the holotype.SVL: 99.3, TL: 168.0, HL: 26.9, HW: 14.5, HH: 15.5, TrL: 42.5, HLL: 66.8, FLL: 37.3, FrL: 6.3, FrW: 3.4.An adult male preserved in formalin in a good state of preservation ( Fig. 4); head and body moderately depressed; tail long, ca. 1.7 times longer than the body, cylindrical and depressed at the base. Head relativelylong (HL/SVL, 0.27) ( Fig. 4), ca. 1.7 times longer than wide (HW/HL, 0.58), head height slightly less than head width (HH/HW, 0.89). Limbs strong, hindlimbs ca. 1.8 times longer than the length of forelimbs (FLL/HLL, 0.56), hindlimbs comprise 1.4 times of the body length (HLL/SVL, 0.67). Head slightly broader than the neck.Head shields including nasals,frontonasal,prefrontals,frontal,frontoparietals, interparietal and parietals are smooth and convex. Nasals moderately swollen, three nasals, the lower in contact with two supralabials on both right and left side and in contact with the rostral ( Fig. 4D). Supranasals in contact with rostral but lack such contact with first supralabial, the suture between them is 3.7 times the length of frontonasal, whose breadth is slightly more than its length; length of prefrontals 1.6 times its width, forming a median suture; length of frontal ca. 1.8 times as long as broad, its length slightly less than its distance from the tip of the snout, narrow behind; parietals smooth, slightly longer than its width; interparietal smooth, more than half the length of frontoparietals, about equal to the suture of frontoparietal; no occipital. Two large supraoculars, about equal in size, the space anterior to supraoculars filled by few small and three to five larger granules; both supraoculars in contact with frontal of their sides while separated from supraciliaries by a series of granules ( Fig. 4C); six supraciliaries, first longest, its length shorter than its distance from the first loreal. Rostral pentagonal, broader than high, narrower beneath than above; anterior loreal slightly higher than wide, shorter than the second loreal which is longer than high; supralabials 10 on the right side, 9 on the left side; subocular keeled just below the eye, bordering the mouth, wedged between sixth and seventh supralabials on the right side and fifth and sixth supralabials on the left side ( Fig. 4D). Temporals smooth, a large scale above ear; auricular denticulation indistinct or three small scales forming slight denticulation anteriorly. Lower eyelid covered with numerous small semi-transparent scales. Six infralabials on the right side, seven on the left side, gradually increasing in size posteriorly. Five pairs of chin shields; anterior three completely in contact, the fourth pair separated by 10 to 11 smaller gulars in a straight line, fifth not in contact with infralabials, separated by a single row of scales. Collar curved, free, serrated and composed of ten plates larger than adjacent gulars, the middle one quite enlarged than others. Gular fold distinct, 32 gular scales in a straight line between the symphysis of the chin shields and the collar ( Fig. 4B). Dorsal scales granular, smooth, 62 across the middle of the body. Ventral plates broader than long (except for outermost series), forming oblique longitudinal series of 16 plates across mid-belly and 29 transverse rows counted from behind collar to vent; first three rows of ventral scales in the pectoral region behind collar longer than broad, the first row is twice as long as broad. Precloacal region with a pair of the enlarged median plates just above the vent, surrounded by six large scales. Forelimb ca. 1.4 times longer than the head, the upper surface of the arm with rhombic, smooth scales. Scales on the upper surface of hindlimbs similar to dorsals, equal in size; ventral surface of hindlimbs covered by enlarged plates, the ventral surface of the tibia with one row of very large and one comparatively smaller plates; the tip of the fourth toe reaches to the forelimb and extends to just behind the collar; 21 femoral pores on the right side, most of the left side damaged, the two femoral pore series separated by two scales, length of the interfemoral space not greater than one–fourth length of each row. Toes slender, compressed, with no fringe; subdigital lamellae unicarinate, in a single row of 25 scales under the 4th toe, a total of three scales around the 4 thtoe. Upper caudal scales oblique, truncate, strongly and diagonally keeled, 30 scales in the 9 th–10 thannulus behind the postcloacal granules.  Coloration in life. The adult specimens are grayish in life with four more or less regular rows of black spots on the light dorsum, originating from behind the parietals, smaller on the nape, larger on the middle of the dorsum, disappearing on proximal one-fourth of the tail. The middle two rows of black spots have white spots along each black spot of the rows. On each lateral side, a broader dorsolateral dark stripe originates from behind the eye and continues onto the tail with disconnected white ocelli at both margins as well as white ocelli inside the stripe; next to the broader dark stripe, a lateral-most stripe is composed of disconnected black ocelli, originating from behind tympanum and reaching to the hindlimb. Upper parts of both hindlimbs and forelimbs with white and black ocelli. Head gray without any markings or spots; labials white with black markings. Belly and underside of tail creamy white, tail dorsum sandy grayish. The juveniles and subadults are nearly similar in coloration to the adults except for the following details; four longitudinal dark stripes on the body, the outermost originate from anterior parietals on the outer side and continue onto the tail, the innermost originate from the posterior of parietals and merge after running a while on the tail. A broader lateral stripe on each side originates from behind the eye and continues on the lateral side of the body and tail with interspersed white ocelli between the forelimb and hindlimb. The dorsal forelimb and hindlimb are dark gray with white ocelli.  Variations in paratypes. The paratypesof  E. rafiqi  sp. nov.agree with the  holotypewith some differences given in Table 2( Figs. 5, 6). Besides sex, the specimens differ in the arrangement of supralabials i.e. subocular wedged between 6 thand 7 thin all the type series except PMNH 861(between 7 thand 8 th) and PMNH 3724(between 5 thand 6 th). The arrangement of postmentals has a similar pattern in the  paratypesexcept PMNH 855, 861, 837, 3723, 3735and 4054, where the fifth chin shield is in contact with the infralabials. The contact of postmental shield with the supralabials varies in the  paratypes; PMNH 855and 3724, the fifth postmental shield is in contact with 7 thsupralabial; PMNH 837and 3735, the fifth postmental shield is in contact with sixth supralabial; PMNH 861, the fifth postmental shield is in contact with 7 thand 8 thsupralabials. The infranasal scale in PMNH 837, 855, 859, 861, 3723, 3735, 4053–4054and 4058 rests on first, second and third supralabials. The scale count of dorsals, ventrals, gulars, collars, caudals at 9 th–10 thannuli and lamellae under 4 thtoe, however, show a unique value for every specimen within a certain range.  Sexual and age dimorphism. Apparently, males attain larger sizes than females in  E. rafiqi  sp. nov.: male SVL to 99.3 mm, female SVL 82.1 mm. Moreover, males have generally longer hindlimbs and shorter trunks as compared to females. For a larger female having SVL of 98.1 mm(PMNH 4058), the hindlimb is 56.0 mm against a smaller-sized male (PMNH 855, SVL 92.2 mm) which has a hindlimb length of 57.1 mm. Similarly, the trunk length of a smaller female (PMNH 3724, SVL 75.1 mm) is 36.8 mmagainst a larger male (PMNH 857, SVL 78.5 mm) which has a trunk length of 34.5 mm. The dorsal body color and pattern, however, varies in juveniles and adults of both genders ( Figs. 5, 6).  Comparison. The new species  Eremias rafiqi  sp. nov.is strikingly different from species exhibiting striped and ocellate patterns in the subgenus  Aspidorhinus(  E. kopetdaghica Szczerbak, 1972,  E. lalezharica Moravec, 1994,  E. papenfussi Mozaffari et al., 2011,  Eremias persicaBlanford, 1874,  E. regeli Bedriaga, 1905,  E. fahimii Mozaffari et al., 2020,  E. isfahanica Rastegar-Pouyani et al., 2016,  E. montanaRastegar-Pouyani & RastegarPouyani, 2001,  E. nikolskii Bedriaga, 1905,  E. veloxPallas, 1771) and ocellate pattern (  E. killasaifullahi  sp. nov.,  E. afghanistanicaBöhme & Szczerbak, 1991,  E. roborowskii Bedriaga, 1912,  E. strauchi Kessler, 1878,  E. suphani Başoğlu & Hellmich, 1968). The new species  E. rafiqi  sp. nov.can also be differentiated from the geographically closely-distributed members of the subgenus  Eremiashaving striped and ocellate pattern (  E. aria Anderson & Leviton 1967) and ocellate pattern (  E. nigrocellata Nikolsky 1896) by the arrangement of subocular scale which borders the mouth (Supplementary Tab. 1; see published data in Lantz 1928, Szczerbak 1974, Bischoff & Böhme 1980, Böhme & Szczerbak 1991, Anderson 1999). A brief of morphological differences is provided (the material used for a first-hand comparison is listed in parentheses at each species; see also Table 2and S 1). Besides striped and ocellate body pattern ( vs.ocellate),  E. rafiqi  sp. nov.can be distinguished from  E. afghanistanicaby its larger size (SVL up to 99.3 mm vs.67.0 mm), higher count of dorsals (56–67 vs.44–46), gulars (30–36 vs.25–28), femoral pores (17–22 vs.16–18), caudal scales in the 9 th–10 thannulus (24–33 vs.22–25), 5–7 supralabials (mainly 6, rarely 5) located anterior to subocular ( vs.5) and lower number of ventral scales in a single row from the posterior edge of collar to the vent (29–33 vs.37–38). From  E. persica, that is partly close in dorsal coloration, pattern and size,  E. rafiqi  sp. nov.differs in the length of interparietal to the length of suture of parietals (longer vs.shorter), length of frontonasal to its width (longer vs.as long as wide), size of the second loreal scale to first loreal scale (more than three times vs.two times), supracaudals (strongly keeled vs.weakly keeled) and tail coloration in the juveniles (sandy grayish vs. bluish). Besides distant distribution,  Eremias rafiqi  sp. nov.differs from the recently described  E. fahimiiby its larger size (SVL up to 99.3 mm vs.56.0 mm), more SDLT 4 th(22–27 vs.20–21), the greater number of scales separating the femoral pores (1–4 vs.1) and the dorsal color and pattern in adults (dorsal stripes broken into ocelli vs.dorsal stripes persistent throughout life). From  E. isfahanica,  E. rafiqi  sp. nov.differs in the following morphological characters apart from its distant distribution: higher count of supralabials (8–10 vs.6–8), 5–7 (mainly 6, rarely 5) of them located anterior to subocular ( vs.5), lower count of collars (8–12 vs.12–15) and the dorsal color pattern in adults (dorsal stripes broken into ocelli vs.dorsal stripes persistent throughout life).   Eremias rafiqi  sp. nov.differs from  E. kopetdaghicain having a higher count of dorsals (56–67 vs.48–59), gulars (30–36 vs.19–28), caudal scales in the 9 th–10 thannulus (24–33 vs.20–26) and collars (8–12 vs.7) and the dorsal color and pattern in adults (presence of a broader dark stripe on each lateral side above flanks with disconnected white ocelli at the margins as well as white ocelli inside the stripe vs.no such lateral broader stripes).   Eremias rafiqi  sp. nov.can be distinguished from  E. lalezharicain having a higher count of dorsals (56–67 vs.54–59), femoral pores (17–22 vs.15–19), pair of chin shields/ submaxillary shields (5 vs.4), lower number of collars (8–12 vs.13–15), contact of gulars with second pair of submaxillary shields (none vs. 1-2 rows of gulars with the second pair of submaxillary shields) and dorsal color and pattern. Apart from its peculiar distribution in the remote valley in Torghar Mountains, a part of the Palearctic region,  E. rafiqi  sp. nov.can be differentiated from  E. montanain the following set of characters: larger size (SVL up to 99.3 mm vs. 58.5 mm), higher count of ventral scales in a row across mid-belly in the widest part (14–17 vs.13–14), number of ventral scales in a single row from the posterior edge of collar to the vent (29–33 vs.27–28), gulars (30–36 vs.23–25), infralabials (6–10 vs.4–6), number of supralabials anterior to the subocular (5–7 vs.4–5), generally more SDLT 4 th(22–27 vs.18–25), generally higher count of scales separating the femoral pores (1–4 vs.2) and dorsal color and pattern. From  E. nigrocellata,  E. rafiqi  sp. nov.differs in dorsal body pattern (striped and ocellate vs.ocellate), higher count of dorsals (56–67 vs.42–56), lower number of ventral scales in a row across mid-belly in the widest part (14–17 vs.18) and the number of femoral pores on each side (17–22 vs.11–13).   E. rafiqi  sp. nov.differs from  E. nikolskiiby having a higher count of gulars (30–36 vs.20–28), ventral scales in a row across mid-belly in the widest part (14–17 vs.14) and dorsal color and pattern. Our new species stands distinguished from  E. papenfussiby its larger size (SVL up to 99.3 mm vs.62.0 mm), higher count of gulars (30–36 vs.24–28), number of scales anterior to subocular (5–7, mainly 6 vs.5), generally higher count of scales separating the femoral pores (1–4 vs.2) and dorsal color and pattern. From  E. regeli,  E. rafiqi  sp. nov.differs in having three scales around the penultimate phalanx of 4 thtoe ( vs.four scales), larger size (SVL up to 99.3 mm vs.70.0 mm), higher count of gulars (30–36 vs.14–24), caudal scales in the 9 th–10 thannulus (24–33 vs.17–25), ventral scales in a row across mid-belly in the widest part (14–17 vs.13), lower count of femoral pores (17–21 vs.21–24) and dorsal color and pattern. The new species  E. rafiqi  sp. nov.can be easily differentiated from  E. strauchiby its distant distribution, color pattern (striped and ocellate vs.ocellate) and larger size (SVL up to 99.3 mm vs.68.0 mm) besides several other characters. From  E. suphani,  E. rafiqi  sp. nov.differs by its distant distribution, color pattern (striped and ocellate vs.ocellate), larger size (SVL up to 99.3 mm vs.60.0 mm) and arrangement of gulars (2 rows of gulars reaching to the second pair of chin shields vs.no such arrangement). The new species  E. rafiqi  sp. nov.can be easily differentiated from  E. veloxby its distant distribution, larger size (SVL up to 99.3 mm vs.77.0 mm), contact of infranasal to rostral (separated vs.in contact), generally higher count of gulars (30–36 vs.19–33) and dorsal color and pattern. From  E. killasaifullahi  sp. nov.,  E. rafiqi  sp. nov.differs in the following morphological characters: color pattern (striped and ocellate vs.ocellate), larger size (SVL up to 99.3 mm vs. 70.5 mm), contact of infranasal with the rostral (in contact vs.separated), a higher number of ventral scales in a single row from posterior edge of collar to the vent (29–33 vs.25–29) and a generally higher count of gulars (29–33 vs.20–33).   Distribution.The evolutionary clade corresponding with the new species  E. rafiqi  sp. nov.was genetically confirmed from the areas of SE Iran(Zabol in the Sistan Basin, Sistan and Balochistan Province; the Zabol clade sensu Rastegar-Pouyani et al. 2010), NW Balochistanin Pakistanand south-central Afghanistan( Rastegar-Pouyani et al.2010, Khan et al.2021). In Pakistan, the species is found in three Pakistani districts located along with the Afghan border including Torghar Mountains in the localities of Tanishpa village and Kunder area (Killa Saifullah district), Ashewat (Qamar Din Karez, Zhob district) and Khar in Nushki District.  Habitat and natural history.The type locality and the localities of paratypes(Tanishpa, Kunder and Ashewat) of  E. rafiqi  sp. nov.are located in the Torghar mountains (means “Black Mountains”), constituting the northern-most part of Toba Kakar Range which is a southern offshoot of the Sulaiman Mountains in the Hindu Kush Mountain system, lying ca. 60 kmfrom the border with Afghanistan( Fig. 7A). The Torghar mountains are very rugged semiarid sandstone ridges with an average elevation of 2,400 mand is approximately 90 kmlong and vary from 15 to 30 kmin width. This region is characterized by having dry temperate ecology, with sparse vegetation. A great deal of information about the Torghar mountains including annual weather conditions, ecology, vegetation and sympatric fauna is provided in Masroor et al.(2020b). The species is also found in the Nushki district, ecological part of the Chagai desert (Registan desert, Afghanistan), lying ca. 340 kmin aerial distance from the Torghar mountains. All the specimens were collected between 11:00 am to 02:00 pm. Interestingly, specimens in the Tanishpa, Kunder and Ashewat were caught in the barren area of mixed loamy and sandy habitats at the foothills of Torghar mountains ( Figs. 7B, C). On the other hand, specimens in the Khar (Nushki district) were collected mostly from the alluvial plain, with dominant vegetation of  Haloxylon persicum, Lyceumshawii, Saccharum griffithii, Chenopodiumalbum, Periploca aphylla, Euphorbia prostrataand others. 3890222325 1997-05-25 PMNH Khalid Javed Baig Tanishpa village 2506 31.1869 Killa Saifullah district 6 68.4126 Torghar Mountains 15 70 PMNH 856 1 Balochistan holotype 3890222324 [419,1099,1790,1817] PMNH Rag Rag 15 70 PMNH 855 1 paratype 3890222329 PMNH Rag 15 70 PMNH 859 1 paratype 3890222337 [208,590,1826,1853] PMNH Rag 15 70 PMNH 861 1 paratype 3890222339 MT554487 [602,1203,1826,1853] MT Females Rag 15 70 PMNH 4056 1 paratype 3890222318 MT554476 MT Rag 15 70 PMNH 3724 1 paratype 3890222308 MT554461, MT554477 [426,1015,1862,1889] MT Rag 15 70 PMNH 3735 1 paratype 3890222310 PMNH Juveniles Rag 15 70 PMNH 4058 1 paratype 3890222313 [279,673,1898,1925] PMNH Rag 15 70 PMNH 837 1 paratype 3890222304 MT554470, MT554496 [686,1279,1898,1925] MT Rag 15 70 PMNH 3723 1 paratype 3890222342 MT554457, MT554485 MT Rag 15 70 PMNH 4053 1 paratype 3890222314 MT554454, MT554480 [595,1181,1934,1961] MT Rag 15 70 PMNH 4054 1 paratype 3890222306 PMNH 15 70 PMNH 857 1 holotype 3890222315 1997-05-26 PMNH Khalid Javed Baig Ashewat 31.3448 Zhob district 6 68.6307 Qamar Din Karez 15 70 PMNH 855 1 paratype 3890222312 1997-05-24 PMNH Khalid Javed Baig Tanishpa village 16 71 Killa Saifullah district Torghar 15 70 PMNH 859 1 paratype 3890222330 2017-10-09 PMNH Muazzam Ali Khan 29.5879 Nushki district 6 65.6609 Khar 16 71 PMNH 3723-24 1 Balochistan paratype 3890222331 [439,1342,186,213] 2017-10-21 PMNH Muazzam Ali Khan Nushki district Khar 16 71 PMNH 3735 1 Balochistan paratype 3890222311 2018-09-05 PMNH Rafaqat Masroor Zamkai Nala 31.193 Torghar 6 68.4111 Tanishpa village 16 71 PMNH 4053 1 Balochistan paratype 3890222340 2018-09-01 PMNH Rafaqat Masroor Ashewat Zhob district Qamar Din Karez 16 71 PMNH 4054 1 Balochistan paratype 3890222307 [262,1303,294,321] 2018-08-30 PMNH Ibad Kunder Killa Saifullah district Torghar 16 71 PMNH 4056 1 Balochistan paratype 3890222326 Rehman 16 71 1 Balochistan paratype 3890222322 PMNH 19 74 18 73 PMNH 861, PMNH 3724 1 holotype 3890222320 PMNH 19 74 PMNH 855, 861, 837, 3723, 3735 1 paratype 3890222332 PMNH 19 74 PMNH 855, PMNH 837, PMNH 861, 855, 859, 861, 3723, 3735, 4053-4054 1 paratype