Long-term population dynamics of marine invertebrates can be shaped by environmental conditions as well as biotic factors, including predation, diseases, interspecific or intraspecific competition. Towards the northern edge of species ranges the role of biotic interactions gradually decreases while the impact of climate oscillations becomes more important. This study examined the long-term changes in abundance, individual growth rates and shell shape characteristics of Macoma balthica, one of the dominant species in White Sea soft-bottom intertidal communities. To test the role of predators in changes in clam abundance, we examined the number of moonsnails Amauropsis islandica. Macoma balthica exhibited spatially synchronous population dynamics at six sites in Kandalaksha Bay, where densities of clams varied between 140 and 8500 ind. m−2 during the 21-year period of observations. Statistical modelling using generalized additive models (GAM) shows that a combination of mild winter and warm summer led to an increase in M. balthica density the following year. Predation by A. islandica had no impact on changes in M. balthica density. Growth rates of M. balthica were higher during a cool decade, but clams that lived in a warmer period were characterized by more globose shells. Our results suggest that the climate oscillations can be regarded as the key factor causing the shift in abundance of M. balthica in the White Sea during the last two decades via recruitment and survival.

Density distribution of the common infaunal bivalves, Macoma balthica and Cerastoderma edule, was studied along the Murman Coast of the Barents Sea during 2002–2010. In both species, abundance was generally higher in West Murman in contrast to East Murman. Highest density of Macoma balthica reaching 1535 ind. m−2 was observed in the Kola Inlet. Cerastoderma edule was less abundant; its density rarely exceeded 10 ind. m−2 in all but one site, where 282 ind. m−2 was registered. Reconstruction of abundance distribution across the European geographic range of Macoma balthica revealed that it does not match an ‘abundant-centre’ pattern, having features of ramped north. On the other hand, distribution of Cerastoderma edule abundance across the range generally follows an ‘abundant-centre’ pattern but southern edge populations show relatively higher abundances as compared with those at the north edge (the Barents Sea).

Many size-selective predators switch their diet during ontogeny. At the White Sea, the adult moonsnails Amauropsis islandica feed mostly on Macoma balthica clams. The diet of juveniles was largely unknown. We conducted a field survey and a caging experiment to find out if juvenile moonsnails can prey on Hydrobia ulvae, and whether they prefer this snail to their usual prey. Live molluscs and their intact or perforated shells were collected from 34 sediment cores. We exposed the single-prey cages with 50 Macoma (MP) or 50 Hydrobia (HP) together with five Amauropsis juveniles, as well as the cages where both prey species were in a 25:25 proportion (HMP). While live Hydrobia was more abundant in the natural assemblages, Amauropsis preferred Macoma, as indicated by proportions of perforated shells. The caging experiment produced similar results. Per capita Macoma consumption rate was significantly higher than Hydrobia consumption rate (6.4 ± 0.5 mg day−1 ind.−1vs. 1.4±0.2 mg day−1 ind.−1 in MP and HP respectively). Prey consumption rates in the single-prey treatments were higher than in mixed-prey cages regardless of prey species. Different mechanisms explain this variation: for Hydrobia it is a consequence of the dietary shift, while for Macoma it reflects the ‘floor’ effect in HMP cages, where virtually all Macoma had been drilled by the end of exposure term. While Macoma is the preferable prey of young Amauropsis, Hydrobia can supplement the diet of juveniles when Macoma is scarce in certain locations.