Genetic data were used to measure the phylogeographic distribution of the limpet, Cellana toreuma along the China coast in order to acsertain impacts of historic events, ocean currents and especially freshwater discharge from the Yangtze River on the connectivity of intertidal species with limited larval dispersal capability. Genetic variation in 15 populations of C. toreuma (n = 418), ranging from the Yellow Sea (YS), East China Sea (ECS) and South China Sea (SCS), were determined from partial mitochondrial cytochrome c oxidase subunit I gene. Genetic diversity and divergence based on haplotype frequencies were analyzed using CONTRIB, and AMOVA was used to examine genetic population structure. Historic demographic expansions were evaluated from both neutrality tests and mismatch distribution tests. Among the 30 haplotypes identified, a dominant haplotype No. 1 (H1) existed in all the populations, and a relatively abundant private haplotype (H2) in YS. Pairwise F_ST values between YS and the other two groups were relatively high and the percentage of variation among groups was 10.9%. The high nucleotide and gene diversity in the YS, with large pairwise genetic distances and relatively high percentages of variation among groups, suggests that this group was relatively isolated from ECS and SCS. This is likely driven by historic events, ocean currents, and demographic expansion. We propose that freshwater discharge from the Yangtze River, which may act as physical barrier limiting the southward dispersal of larvae from northern populations, is especially important in determining the separation of the YS group from the rest of the Chinese populations of C. toreuma.

Cultured free round pearls are produced by implanting a spherical nucleus with a small piece of nacre-secreting mantle graft from a donor oyster into the gonad of a recipient oyster (host). To examine the possible contribution of host and donor oysters to the colouration of the harvested pearls, the CSE-1 Imaging and Color-Measuring System were used to quantitatively measure the L*a*b* values of donor and host shells and the produced pearls in Pinctada martensii. Results showed that the colour of pearls had significant positive correlation (r = 0.1–0.22, P = 0.00) with that of donors, but had no correlation with that of host oysters, thus convincingly confirmed the contribution of nacre colour of donor to the realization of pearl quality of colour. To further clarify the relationship between the donor and the pearl colour, the donors from pearls of good and poor colour quality were further compared and the results demonstrated the significant difference in L* values (P < 0.05) and insignificant difference in a* and b* values, suggesting the necessity of selecting donors with bright and lustrous nacre in pearl production.

Pearl sac is the tissue that secretes proteins resulting into artificial pearl formation, a highly controlled biomineralization process similar to development of inner shell regulated by the mantle. We present here the pearl sac transcriptome of Pinctada fucata martensii using massively parallel pyrosequencing. A total of 21 729 putative unique transcripts were assembled and annotated. Twenty-three candidate biomineralization genes were identified, such as calmodulin, calponin-like protein (CLP), mantle gene, pearlin, nacrein and Pif. The sequence data contained 4303 potential SNP loci and 4291 probable indels, providing a resource for molecular biomarker, population genetics and gene function. Expression levels of six potential biomineralization genes were also characterized with real-time PCR. The expression level of mantle gene 4 was the highest, followed by lysine-rich matrix protein 4. Nearly all detected genes maintained the highest expression levels in mantle edge and the lowest in pearl sac. In both tissues of mantle centre and pearl sac, the six genes had an obvious higher expression activity in host oyster producing nacre pearls than those producing plain nuclei, but the expression level of CLP was similar in the two host groups. These results will notably advance biomineralization and transcript-wide study in P. fucata martensii and other Pinctada species.