We monitored testicular and ovarian morphologies, seminiferous tubules, the sexual segments of the kidneys (SSK), follicular histologies, and male testosterone and female estradiol to define the reproductive pattern of Calotes emma and Calotes versicolor. Samples were collected monthly at Sakaerat Environmental Research Station in Thailand for 1 year. Testicular hypertrophies occurred at a time characteristic for each species, with their time course corresponding well to both active spermatogenesis and the hypertrophied SSK. Gravid females were also found at a time characteristic for each species. In active reproductive females, oviductal eggs were concomitantly encountered with ovarian vitellogenic follicles. The previtellogenic and vitellogenic follicles corresponded well to granulosa layer alterations. The distinct large pyriform cells were present in the granulosa layer of previtellogenic follicles but disappeared from the vitellogenic follicles. Male testosterone levels rose during testicular and SSK hypertrophies, and female estradiol levels increased during active reproductive stages of late vitellogenic follicles and gestation. We suggest that the reproductive patterns of C. emma and C. versicolor fall into the same reproductive pattern of annual continual reproduction, but that the time courses of such events are different in the 2 Calotes, and even in individuals of the same Calotes population.

We describe Gekko pradapdao sp. nov. from Tham Khao Chan (Khao Chan Cave), Tha Luang District, Lopburi Province, in central Thailand. The new species, a member of the subgenus Gekko, differs from all currently recognized Gekko species by the following combination of morphological characters and pattern: maximal known snout-vent length of 127.1 mm, lack of contact between nostrils and rostral, 24–28 interorbital scales between supraciliaries, 89–91 scale rows around midbody, 16–18 dorsal tubercle rows at midbody, 30–34 ventral scale rows at midbody, 11–13 precloacal pores in males, a single postcloacal tubercle on each side of the base of the tail, 13–16 subdigital lamellae on 1st toe and 17–19 on 4th toe, no Y-shaped mark on head, non-banded dorsal pattern on a dark chocolate brown to black background, and a dark brown iris. Urgent actions should be taken to evaluate the conservation status of the new species.

The blue swimming crab (Portunus pelagicus) is a valuable commercial species. In Thailand, the consumption of the blue swimming crab is increasing. To construct an effective sustainable management plan, genetic information is required. Knowledge of natural stock genetic information can help policymakers design fishing and conservation management policies to maintain genetic diversity. In our study, we examined the genetic structure of the blue swimming crab population on the Andaman Sea coast of Thailand. Partial sequences of the mitochondrial DNA control region (mtDNA CR) with a size of 369-371 base pairs were studied in 150 individuals collected from five sampling sites along Thailand's Andaman Sea coast. Seventy-one haplotypes were characterized by 127 polymorphic sites, indicating high haplotype diversity but low nucleotide diversity across five localities. The multiple tests of population genetic analysis showed a lack of genetic structure. The absence of genetic structure was possibly caused by a high level of gene flow due to the larval blue swimming crab's high dispersal ability. Demographic history findings indicate that the blue swimming crab population has expanded. The findings of our study can be used to guide the management of the blue swimming crab in this region of the Andaman Sea to conserve genetic diversity.

We describe Gehyra wongchan sp. nov. from Tham Khao Chan (Khao Chan Cave), Tha Luang District, and Wat Khao Wong, Kok Samrong District, in Lopburi Province, central Thailand. The new species differs from all currently recognized Gehyra by the following combination of morphological characters and dorsal color pattern: maximal known snout–vent length of 52.4 mm, 8–10 supralabials, 76–80 dorsal and 48–50 ventral scale rows around midbody, absence of skin folds on limbs, 17 or 18 preanofemoral pores in males in a continuous series extending to mid-length of femur (pores absent in females), tail not- to moderately widened behind vent in adults, a single row of widened subcaudals, digits and toes unwebbed, 7 or 8 divided subdigital lamellae on 4th toe, and a dorsal pattern with white spots as large or larger than adjacent crescentic black markings on a beige to light-brown background.