No abstract

Summary Length‐weight relationships (LWRs) were determined for eleven endemic fish species [Coreius guichenoti (Sauvage & Dabry de Thiersant, 1874), Glyptothorax sinensis (Regan, 1908), Leptobotia elongata (Bleeker, 1870), Leptobotia taeniops (Sauvage, 1878), Pseudobagrus crassilabris (Günther, 1864), Rhinogobio ventralis (Sauvage & Dabry de Thiersant, 1874), Saurogobio dabryi (Bleeker, 1871), Schizothorax chongi (Fang, 1936), Schizothorax kozlovi (Nikolskii, 1903), Schizothorax prenanti (Tchang, 1930) and Schizothorax wangchiachii (Fang, 1936)] from the middle reaches of the Jinsha River in southwest China. Samples were obtained between May 2004 and July 2013 using various types of fishing gear and electroshock fishing techniques. For each species, the sample size, length range, weight range, LWR, 95% confidence intervals of a and b, and coefficient of correlation were determined. Prior to this study, the LWRs for four species (P. crassilabris, S. chongi, S. kozlovi and S. prenanti) were unknown.

Seven new microsatellite markers were developed for the Pacific abalone (Haliotis discus hannai, Haliotidae), and allelic variability was compared between a wild population and a hatchery population in Yeosu, Korea. All loci amplified readily and demonstrated allelic variability, with the number of alleles ranging from 6 to 15 in the wild population and from 3 to 12 in farmed populations. Average observed and expected heterozygosities were estimated at 0.65 and 0.77 in the hatchery samples, and 0.79 and 0.87 in the wild samples. These results indicated lower genetic variability in the hatchery population, as compared with the wild population and significant genetic differentiation between the wild population and the hatchery samples (FST=0.055, p<0.001). These microsatellite loci may be valuable for future population genetic studies and for tracking hatchery samples used in stock enhancement programs.

ABSTRACT. Manila clam (Ruditapes philippinarum) is a valuableand intensively exploited shellfish species in Korea. Despite its importance, information on its genetic background is scarce. For the genetic characterization of R. philippinarum, expressed sequence tagderived microsatellite markers were developed using next-generation sequencing. A total of 5879 tandem repeats containing di-to hexanucleotide repeat motifs were obtained from 236,746 reads (mean = 413 bp). Of the 62 loci screened, 24 (38.7%) were successfully amplified, and 10 were polymorphic in 144 individuals from 2 manila clam populations (Incheon and Geoje, Korea). The number of alleles ranged from 2 to 17 in the Incheon population and from 3 to 13 in the Geoje population (overall A R = 7.21). The mean observed and expected heterozygosities were estimated to be 0.402 and 0.555, respectively. Hence, there is less genetic variability in the Geoje population than in the Incheon population, although no significant reductions of genetic diversity were found between the populations (P > 0.05). However, significant genetic differentiation was detected between the populations (F ST = 0.064, P < 0.001). Significant deviations from Hardy-Weinberg equilibrium and high inbreeding coefficients (mean F IS = 0.22-0.26) were detected in both populations. The 10 novel polymorphic microsatellite loci used in this study will be useful for future genetic mapping studies and for characterizing population structures, monitoring genetic diversity for successful aquaculture management, and developing conservation strategies for manila clam populations in Korea.