Saxidomus purpuratus (S. purpuratus) is an economically important bivalve along the northern coast of China, where intensifying fishing pressure threatens its wild stocks. Its genome-wide population genetic variation remains poorly characterized. We resequenced 75 wild individuals from five populations spanning the northern Yellow Sea (Donggang, DDDG; Ganjingzi, DLGJ; Huancui, WHHC) and the Bohai Sea (Changdao, YTCD; Laizhou, YTLZ). The sampled populations exhibited relatively low genetic diversity (He = 0.1301–0.1324), weak among-population differentiation (Fst = 0.0035–0.0040), and heterozygosity deficiency (Fis = 0.0480–0.0831). PCA, NJ, and ADMIXTURE detected no geographic structure. PSMC revealed concordant demographic histories, with a sustained decline following a Middle Pleistocene expansion, consistent with historical allele exchange. Selection scans (DDDG as the target population; WHHC and YTCD as references) identified 1268 candidate genes, of which 197 were shared across the two comparisons. After masking a tandem histone gene cluster, the remaining 155 non-histone genes fell into five functional categories: receptor and signal transduction, membrane transport and ion channels, innate immunity and defense, extracellular matrix and adhesion, and detoxification and metabolism. These signals recurred in both comparisons, identifying DDDG as a candidate population for genotype–environment association testing. Together, these results provide the first genome-wide assessment of S. purpuratus and indicate that the five populations constitute a single genetically connected unit, while pinpointing a small set of candidate loci that may underpin local adaptation and warrant monitoring in stock-enhancement programmes.
No takes yet. Share an insight, caveat, or question.
Xu et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: