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An integrative taxonomic study recognized a new species of the Cyrtodactylus pulchellus group from Kanchanadit District, Surat Thani Province, Southern Thailand. Phylogenetic analyses of the mitochondrial ND2 gene revealed a new species, Cyrtodactylus kanchanaditsp. nov., that is closely related to C. lekaguli. The new species differs from its sister lineage by bearing mean genetic divergence of 4.53% and significant differences in both mensural and morphometric characters (p < 0.05). Cyrtodactylus kanchanaditsp. nov. can be differentiated from the remaining members of the C. pulchellus species group because of its genetic divergence of ≥7.99% and a combination of differences in body size: 11–15 supralabial and 10–12 infralabial scales, 29–35 paravertebral tubercles, 18–23 longitudinal rows of dorsal tubercles, 32–37 rows of ventral scales, 20–23 subdigital lamellae on the fourth toe, 32–37 femoroprecloacal pores in adult males, and four or five dark body bands; weak tuberculation on body; absence of tubercles in the ventral body fold, absence of precloacal pores in females, and absence of scattered pattern of white tubercles on dorsum; presence of precloacal groove depression; and maculated white caudal bands. Cyrtodactylus kanchanaditsp. nov. is currently known from its type locality.

A new karst-dwelling bent-toed gecko of the Cyrtodactylus intermedius group is described from Khlong Hat District, Sa Kaeo Province, eastern Thailand, based on an integrative taxonomic analysis of genetic data and morphological characteristics. Phylogenetic analyses using the mitochondrial NADH dehydrogenase subunit 2 (ND2) gene revealed that topotypes of C. intermedius were sister to a clade containing C. kulenensis from Cambodia, an unnamed lineage from Sakaerat Biosphere Reserve in Nakhon Ratchasima Province, Thailand, and the Khlong Hat lineage described here as Cyrtodactylus khlonghatensis sp. nov. Multivariate analyses of morphometric and meristic characters showed that C. khlonghatensis sp. nov. is morphologically distinct from all other species in the group by having the combination of SVL 76.5–82.8 mm in adult males and 88.5 mm in an adult female; eight supralabial and nine infralabial scales; 30–32 paravertebral tubercles; 20 or 21 longitudinal rows of dorsal tubercles; 43 or 44 ventral scales; seven or eight expanded subdigital lamellae on the 4 th toe; 12 unmodified subdigital lamellae on the 4 th toe; 19 or 20 total subdigital lamellae on the 4 th toe; 31 or 32 total number of enlarged femoral scales; enlarged femoral and precloacal scales continuous; 6–8 pore-bearing precloacal scales in males; three or four rows of enlarged post-precloacal scales; 1–3 postcloacal tubercles; proximal femoral scales less than one-half the size of distal femoral scales; absence of interdigital pocketing between digits of forefeet and hindfeet; and posterior border of the nuchal loop rounded. Uncorrected pairwise genetic divergences ( p -distances) between the new species and other species of the intermedius group ranged from 4.73–22.55%. The discovery of this new species exclusively in isolated karst formations from the Thai-Cambodia border suggests that there may be further undiscovered Cyrtodactylus in unexplored karst landscapes along the border of eastern Thailand and western Cambodia.

Species delimitation and species diagnosis must remain separate operations to avoid constructing taxonomies comprised of non-monophyletic species based on morphological similarity as opposed to phylogenetic propinquity. This is particularly true for highly specialized species such as the range-restricted upland taxa in the Cyrtodactylus brevipalmatus group of Indochina where strong selection pressure for an arboreal lifestyle has contributed to morphologically similar but distantly related species. This in turn, has resulted in a history of erroneous taxonomies that have actually obscured rather than revealed the diversity within this group. A Bayesian phylogeny of the C. brevipalmatus group recovered at least 15 putative species-level lineages, at least seven of which are undescribed, and of which four are described herein. A total evidence morphological data set comprised of 16 normalized morphometric, 15 meristic, and seven categorical characters scored across 51 individuals was subjected to a multiple factor analysis (MFA) and an analysis of variance (ANOVA) to diagnose the putative species. These new species descriptions contribute to focusing attention to the unrealized diversity in upland tropical ecosystems, which due to climate change, are some of the most impearled ecosystems on the planet. Thus, it is paramount that taxonomies do not conflate species identities and underrepresent true diversity.

A new species of the Cnemaspis siamensis group is described from Wang Khrachae District, Kanchanaburi Province, western Thailand based on morphological and molecular data. The new species, Cnemaspis enneaporus Rujirawan, Aksornneam & Aowphol, sp. nov. , is distinguished from other species in the C. siamensis group by having the combination of SVL 42.2 mm in adult male ( n = 1), 43.7 mm in adult female ( n = 1); eight supralabials; seven or eight infralabials; ventral scales smooth; nine continuous precloacal pores in male; 17 or 18 paravertebral tubercles linearly arranged; tubercles on lower flanks present; lateral caudal furrows present; no caudal tubercles in the lateral furrows; ventrolateral caudal tubercles present on original portion of tail; caudal tubercles not encircling tail; subcaudals smooth; no enlarged median subcaudal row; two postcloacal tubercles on each side of tail; no shield-like subtibial scales; subtibial scales smooth; no enlarged submetatarsal scales; 26–28 subdigital lamellae on the fourth toe; sexually dimorphic for dorsal and ventral colour pattern; prescapular marking absent; gular marking absent; and yellow colouration in life on all ventral surfaces of head, body and tail in adult male. Phylogenetically, the new species is recovered as the sister taxon to C. huaseesom , but the two species are separated by 8.3–9.4% uncorrected pairwise genetic divergences in the mitochondrial NADH dehydrogenase subunit 2 gene and flanking tRNAs.

The exploration of unsurveyed areas in southern Thailand discovered two new karst-adapted species, Cyrtodactylus sungaiupe sp. nov. and Cyrtodactylus wangkhramensis sp. nov. , from Thung Wa and La-ngu Districts, Satun Province, respectively. These new species are members of the C. pulchellus group that occur along the Thai-Malay Peninsula. The new species can be distinguished from all other congeners by their key morphological characters and genetic divergence. Morphologically, Cyrtodactylus sungaiupe sp. nov. and Cyrtodactylus wangkhramensis sp. nov. can be diagnosed from other members by having a combination of differences in body size; degree of dorsal tuberculation; absence of tubercles on ventral surfaces; number of ventral scales, paravertebral tubercles and femoroprecloacal pores in males only; deep precloacal groove only in males; absence of a scattered pattern of white dorsal tubercles; number of dark body bands; and the extent of caudal tubercles on an original tail. Although the two species are sister taxa and have nearly identical morphologies, they are considered to be different species, based on a relatively high uncorrected pairwise genetic divergence of the mitochondrial ND2 gene (6.59–6.89%), statistically significant univariate and multivariate morphological differences (PERMANOVA and ANOVA) and diagnostic characteristics of caudal tuberculation on the original tail. Moreover, Cyrtodactylus sungaiupe sp. nov. and Cyrtodactylus wangkhramensis sp. nov. are currently restricted to their karstic type localities which may serve as a geographic barrier to dispersal and gene flow.

An integrative systematic analysis recovered a new species of the Cyrtodactylus brevipalmatus group from the uplands of Thong Pha Phum National Park, Kanchanaburi Province in western Thailand. Cyrtodactylus thongphaphumensis sp. nov. is deeply embedded within the brevipalmatus group, bearing an uncorrected pairwise sequence divergence of 7.6–22.3% from all other species based on a 1,386 base pair segment of the mitochondrial NADH dehydrogenase subunit 2 gene (ND2) and adjacent tRNAs. It is diagnosable from all other species in the brevipalmatus group by statistically significant mean differences in meristic and normalized morphometric characters as well as differences in categorical morphology. A multiple factor analysis recovered its unique and non-overlapping placement in morphospace as statistically significantly different from that of all other species in the brevipalmatus group. The description of this new species contributes to a growing body of literature underscoring the high degree of herpetological diversity and endemism across the sky-island archipelagos of upland montane tropical forest habitats in Thailand, which like all other upland tropical landscapes, are becoming some of the most imperiled ecosystems on the planet.

The taxonomy and geographic distributions of species of crab-eating frogs ( Fejervarya cancrivora complex) in mainland Southeast Asia have been highly uncertain. Three taxonomic names are used in recent literature ( F. cancrivora , F. raja , and F. moodiei ) but the applications of these names to localities has been inconsistent, especially owing to the lack of available molecular data for F. raja . Morphometric and mitochondrial DNA variation was examined in these frogs, including name-bearing types and topotypes of all three species. Findings corroborate evidence for the existence of two species in coastal mainland Southeast Asia, with F. moodiei having a wide geographic distribution and F. cancrivora sensu stricto occurring only in extreme southern Thailand and peninsular Malaysia. Fejervarya raja is shown to be only a large-bodied population of F. cancrivora sensu stricto and is synonymized with that species. Revised descriptions of F. moodiei and F. cancrivora sensu stricto are provided.

We described a new species of elapid snake genus Bungarus from the Tenasserim Mountain Range in Ratchaburi Province, western Thailand. Bungarus sagittatus sp. nov. can be distinguished from all congeners by having the combination of 15 dorsal scale rows; 215–217 ventral scales; 48–56 undivided subcaudal; prefrontal suture 2.4–2.6 times length of internasal suture; anterior chin shields larger than posterior chin shields; head of adult uniform black while juvenile black with small dim white patches on temporal and parietal areas; dorsal body black, with 25–31 white narrow bands, white and black bands at midbody covering 1.5–3.0 and 4.5–6.0 vertebral scales, respectively; dorsal body black bands not intruding ventrals or intruding ventrals less than 0.5 times of width of outer dorsal scales; ventral surface of body immaculate white; ventral side of tail white with a row of dark brown triangular patches on middle pointing posteriorly; tail relatively long, tail length/total length 0.140–0.143. Genetically, the new species has uncorrected pairwise divergences of ≥ 8.29% of the mitochondrial cytochrome b from other Bungarus species. Currently, the new species is only known from the type locality.

Phylogenetic and morphological analyses delimit and diagnose, respectively, a new population of a karst-dwelling Cyrtodactylus from extreme northern Thailand. The new species, Cyrtodactylus phamiensis sp. nov. , of the chauquangensis group inhabits karst caves and outcroppings and karst vegetation in the vicinity of Pha Mi Village in Chiang Rai Province, Thailand. Within the chauquangensis group, Cyrtodactylus phamiensis sp. nov. is the earliest diverging species of a strongly supported clade composed of the granite-dwelling C. doisuthep and the karst-dwelling sister species Cyrtodactylus sp. 6 and C. erythrops . The nearly continuous karstic habitat between the type locality of Cyrtodactylus phamiensis sp. nov. and its close relatives Cyrtodactylus sp. 6 and C. erythrops , extends for approximately 200 km along the border region of Thailand and the eastern limit of the Shan Plateau of Myanmar. Further exploration of this region, especially the entire eastern ~ 95% of the Shan Plateau, will undoubtably recover new populations whose species status will need evaluation. As in all other countries of Indochina and northern Sundaland, the continual discovery of new karst-dwelling populations of Cyrtodactylus shows no signs of tapering off, even in relatively well-collected areas. This only highlights the conservation priority that these unique karstic landscapes still lack on a large scale across all of Asia.

A new species in the dicroglossid frog genus Limnonectes is described from Ko Pha-ngan, Ko Samui, and Ko Lanta Yai Islands in southern Thailand. Males of Limnonectes pseudodoriae sp. nov. lack a caruncle on top of the head and very closely resemble L. doriae (Boulenger, 1887) from Myanmar and western and southern Thailand. However, the new species is distinguished from L. doriae and its congeners using an integrative taxonomic approach of morphology, mitochondrial DNA, and bioacoustics. Limnonectes pseudodoriae sp. nov. differs from L. doriae and its congeners by having a unique combination of morphological characters, including body size; skin texture of the interorbital region, dorsum, and shank; toe webbing; relative size of the inner metatarsal tubercle; and coloration of the tympanum, venter, and ova. The advertisement call of the new species is also readily differentiated from that of L. doriae in temporal parameters. Limnonectes pseudodoriae sp. nov. is highly divergent in mitochondrial DNA from L. doriae and its congeners, but its phylogenetic position within the genus is not resolved. The natural history of the new species is presented, and the geographic range of L. doriae in Thailand is clarified.