Recent climate changes have had marked effects on the ice-free season and thermal conditions in many high-latitude lakes, but their ecological effects combine with density-dependent processes to affect fish growth and life history. To better understand the relative roles of climate and intraspecific density, we applied Gaussian state–space models to long-term data (1962–2006) on growth of juvenile sockeye salmon ( Oncorhynchus nerka ) in Iliamna Lake, Alaska, USA. Both temperature and density influenced fry size at the end of their first growing season, but the positive effect of temperature exceeded the negative effects of density. Fry growth was affected by the magnitude of their own cohort more strongly than by the previous brood (i.e., yearlings). In contrast, density was more important than temperature in Lake Aleknagik, also in Bristol Bay, over the same period of record, probably because Iliamna Lake is cooler and has generally lower densities of juvenile sockeye salmon than Lake Aleknagik. In both lakes, the size of the fish at the end of the first growing season affects smolt size and age at seaward migration, hence survival at sea and age at maturity, so the relative effects of climate and density depend on the ecological context.

A large and growing body of literature has documented the transfer of marine‐derived nutrients from the ocean to freshwater and riparian systems by semelparous Pacific salmon Oncorhynchus spp. The pathways by which these nutrients reach resident fish are often indirect, and the evidence for direct benefits to the resident fish is not always conclusive. However, the consumption of salmon tissue (in one form or another) by resident fish would constitute a direct and efficient pathway for energy transfer. We studied a population of small‐bodied, nonanadromous Dolly Varden Salvelinus malma feeding on the fry and eggs of sockeye salmon O. nerka and blowfly (family Calliphoridae) larvae that had fed on salmon carcasses at a series of spring‐fed and otherwise unproductive ponds in southwestern Alaska. The Dolly Varden fed heavily on sockeye salmon fry when available, shifted their diet almost exclusively to eggs after salmon spawning commenced, and then shifted to blowfly larvae toward the end of the season. Dolly Varden large enough to eat eggs moved into ponds where sockeye salmon spawn synchronously with the arrival of the salmon, and Dolly Varden growth rates increased greatly once salmon eggs and blowfly maggots were available. Young‐of‐the‐year Dolly Varden, which were too small to eat eggs and fry, were concentrated in small streams between ponds where fewer sockeye salmon spawn, perhaps to minimize the risk of predation from larger conspecifics. These results indicate the importance of a pulse of salmon‐related food resources for this population of resident fish and their adaptations to take advantage of these resources. It is likely that similar dependence occurs in other systems where sockeye salmon produce a suite of temporally predictable energy resources; thus, resident fish may depend on large populations of salmon.

In 2004 and 2005, exceptionally large runs of sockeye salmon (Oncorhynchus nerka) to the Alagnak River system in Bristol Bay, Alaska, coincided with weak runs to the nearby Kvichak River system. Restricted fishing to protect the Kvichak populations resulted in densities on the Alagnak River system's spawning grounds that were 11.5-fold (in 2004) and 9.0-fold (in 2005) above the long-term (1956–2003) average. Carcass sampling indicated that 23% (2004) and 44% (2005) of the potential egg deposition was lost to prespawning mortality or incomplete spawning in the Alagnak populations. Much lower levels of egg retentions were observed in spawning populations in the Kvichak River and Wood River systems, where the runs did not appreciably exceed the escapement goals, indicating that density-dependent spawning failure may have occurred. However, in 2005, significantly higher egg retention rates were observed in the Alagnak River system despite slightly lower densities than in 2004, indicating that environmental processes (probably low river levels and high temperatures) influenced prespawning mortality as well. More limited sampling in 2006 revealed only 3% egg retention in one of the Alagnak populations, but the combination of lower density and cooler conditions did not allow us to determine the relative contributions of these two factors to spawning failure.