Megophrys (Xenophrys) zhangi Figures 1 and 3 (d – g); Tables 2, S 1, S 2 specimens examined: CMDN-A 48 – 49, 56 – 59, 64 – 66, 83 – 85, 87 – 88, 98 – 101, 104 – 118, 129 – 150, 154, 164 – 165, 167 – 170. Distribution in the KTM Valley: Encountered at all non-urban localities surveyed. Remarks: We encountered large numbers of Megophrys zhangi around the KTM Valley (Table 2; Figure 1). This species was traditionally classified as Megophrys parva until Chen et al. (2017) assigned several Megophrys species to Xenophrys, including M. parva. Alternatively, Mahony et al. (2017) classified Xenophrys as a subgenus of Megophrys which is the arrangement we favour in this manuscript. Our phylogenetic analyses revealed a close phylogenetic affinity between Megophrys parva from the KTM Valley and M. zhangi (Ye and Fei 1992) from the type locality (Figure 5). The type locality of M. zhangi is Zhangmu, Xizang, China, close to the Nepal-China border in the foothills of the Himalayas ~ 55 km from KTM Valley. However, Mahony et al. (2018) found that this M. zhangi individual (sequenced by Chen et al. 2017) shared an identical 16s haplotype with one of their two M. monticola haplotype groups from Darjeeling (‘ mid-elevation mitochondrial haplotype group ’). Using nuclear sequence data, Mahony et al. (2018) show that the two haplotype groups of M. monticola represent a single species that exhibit deep divergence with M. zhangi. Mahony et al. (2018) suggest that the shared haplotype may represent mitochondrial capture between these sister species. Thus, using 16s sequence we were unable to verify if the Nepalese sequences pertain to M. zhangi or M. monticola, though the geographic proximity to the M. zhangi type locality would support the former hypothesis. However, Mahony et al. (2018) differentiated M. zhangi (using the original description) from M. monticola based on a smaller SVL in the former. They state that in male specimens of M. zhangi (n = 3), SVL = 32.5 – 37.2 mm, compared with those of M. monticola (n = 17), SVL = 38.2 – 49.5 mm. SVL for the KTM Valley Megophrys range from 35 to 43.2 mm, overlapping the ranges given for the two species. However, the PCA of the 10 characters shared between our studies strongly separates the KTM Valley individuals from M. monticola, suggesting that the KTM Megophrys are on average much smaller (Figure 5 (b)). For this reason, we reclassify Megophrys parva from the KTM Valley to M. zhangi. Because we only sequenced specimens from the KTM Valley, we suggest that other Megophrys species may be present in other regions of Nepal outside of the KTM Valley (Mahony et al. 2018). Megophrys zhangi was encountered on the banks of streams and around areas with running water (Figure 3 (g)). While we usually observed them in intact habitats, they were also commonly encountered near disturbed areas with running water, but never in urban areas. Males called as early as 1600 during heavy rain but usually began calling at sundown (1900 in August). Females were found as far as 250 m from water, and always on the ground (Figure 3 (e)). Males perched ~ 1 m above the water when calling, and always faced the water. At each locality males utilised different perch taxa ranging from bushes, to large rocks, to man-made structures (Figure 3 (d,g)). This species was usually encountered in the same localities as Nanorana liebigii, but the two species were never observed in syntopy. At one locality in east Shivapuri, we encountered large numbers of larvae present in a shallow pool along with larvae and a juvenile of Duttaphrynus melanostictus (Figure 3 (f)). Measurements: The mean, followed by the range in parenthesis is given for males (n = 26), followed by females (n = 2). SVL = 39.2 mm (35 – 43.2 mm), 43.8 mm (40 – 47.8 mm); HL = 12.4 mm (10.0 – 14.8 mm), 13.0 mm (11.2 – 14.8 mm); HW = 14.9 mm (12.0 – 17.0 mm), 15.8 mm (14.9 – 16.6 mm); snout = 4.1 mm (3.3 – 5.7 mm), 4.2 mm (3.7 – 4.7 mm); internarial = 5.0 mm (3.8 – 5.8 mm), 4.65 mm (4.6 – 4.7 mm); eye = 3.5 mm (2.5 – 4.5 mm), 4.35 mm (3.9 – 4.8 mm); tympanum = 2.1 mm (1.7 – 2.7 mm), 2.6 mm (2.5 – 2.7 mm); antebrachium = 8.7 mm (7.1 – 10.2 mm), 8.1 mm (7 – 9.2 mm); hand = 10.5 mm (9.2 – 12.0 mm), 12 mm; thigh = 15.2 mm (13.5 – 17.5 mm), 14.5 mm (12.9 – 16.1 mm); shank = 16.8 mm (14.4 – 18.8), 17.1 mm (15.2 – 19 mm); foot = 27 mm (23.7 – 29.3 mm), 28.4 mm (27.6 – 29.1 mm)., Published as part of O, Kyle A., Connell, Aryal, Prakash C., Sherchan, Adarsh M., Dhakal, Bimala, Chaudhary, Hemanta Kumari, Ranabhat, Rishi & Karmacharya, Dibesh, 2019, A herpetological survey of the Kathmandu Valleyı Nepalı and phylogenetic identification of Megophrys (Xenophrys) zhangi, pp. 1421-1437 in Journal of Natural History 53 (23) on pages 1428-1431, DOI: 10.1080/00222933.2019.1655106, http://zenodo.org/record/3670114, {"references":["Chen JM, Zhou WW, Poyarkov NA, Stuart BL, Brown RM, Lathrop A, Wang YY, Yuan ZY, Jiang K, Hou M, et al. 2017. A novel multilocus phylogenetic estimation reveals unrecognized diversity in Asian horned toads, genus Megophrys sensu lato (Anura: Megophryidae). Mol Phylogenet and Evol. 106: 28 - 43. doi: 10.1016 / j. ympev. 2016.09.004","Mahony S, Foley NM, Biju SD, Teeling EC. 2017. Evolutionary history of the Asian Horned Frogs (Megophryinae): integrative approaches to timetree dating in the absence of a fossil record. Mol Biol and Evol. 34: 744 - 771.","Ye CY, Fei L. 1992. A new pelobatid toad of the genus Megophrys from Xizang, China. Acta Herpetol Sinica. 1 - 2: 50 - 52.","Mahony S, Kamei RG, Teeling EC, Biju SD. 2018. Cryptic diversity within the Megophrys major species group (Amphibia: Megophryidae) of the Asian Horned Frogs: phylogenetic perspectives and a taxonomic revision of South Asian taxa, with descriptions of four new species. Zootaxa. 4523: 1 - 96. doi: 10.11646 / zootaxa. 4523.1"]}