Declines in animal body sizes are widely reported and likely impact ecological interactions and ecosystem services. For harvested species subject to multiple stressors, limited understanding of the causes and consequences of size declines impedes prediction, prevention, and mitigation. We highlight widespread declines in Pacific salmon size based on 60 years of measurements from 12.5 million fish across Alaska, the last largely pristine North American salmon-producing region. Declines in salmon size, primarily resulting from shifting age structure, are associated with climate and competition at sea. Compared to salmon maturing before 1990, the reduced size of adult salmon after 2010 has potentially resulted in substantial losses to ecosystems and people; for Chinook salmon we estimated average per-fish reductions in egg production (−16%), nutrient transport (−28%), fisheries value (−21%), and meals for rural people (−26%). Downsizing of organisms is a global concern, and current trends may pose substantial risks for nature and people.
The demographic structure of populations is affected by life history strategies and how these interact with natural and anthropogenic factors such as exploitation, climate change, and biotic interactions. Previous work suggests that the mean size and age of some North American populations of Chinook salmon (Oncorhynchus tshawytscha, Salmonidae) are declining. These trends are of concern because Chinook salmon are highly valued commercially for their exceptional size and because the loss of the largest and oldest individuals may lead to reduced population productivity. Using long‐term data from wild and hatchery populations, we quantified changes in the demographic structure of Chinook salmon populations over the past four decades across the Northeast Pacific Ocean, from California through western Alaska. Our results show that wild and hatchery fish are becoming smaller and younger throughout most of the Pacific coast. Proportions of older age classes have decreased over time in most regions. Simultaneously, the length‐at‐age of older fish has declined while the length‐at‐age of younger fish has typically increased. However, negative size trends of older ages were weak or non‐existent at the southern end of the range. While it remains to be explored whether these trends are caused by changes in climate, fishing practices or species interactions such as predation, our qualitative review of the potential causes of demographic change suggests that selective removal of large fish has likely contributed to the apparent widespread declines in average body sizes.
The average sizes of Pacific salmon have declined in some areas in the Northeast Pacific over the past few decades, but the extent and geographic distribution of these declines in Alaska is uncertain. Here, we used regression analyses to quantify decadal trends in length and age at maturity in ten datasets from commercial harvests, weirs, and spawner abundance surveys of Chinook salmon Oncorhynchus tshawytscha throughout Alaska. We found that on average these fish have become smaller over the past 30 years (~6 generations), because of a decline in the predominant age at maturity and because of a decrease in age-specific length. The proportion of older and larger 4-ocean age fish in the population declined significantly (P < 0.05) in all stocks examined by return year or brood year. Our analyses also indicated that the age-specific lengths of 4-ocean fish (9 of 10 stocks) and of 3-ocean fish (5 of 10 stocks) have declined significantly (P < 0.05). Size-selective harvest may be driving earlier maturation and declines in size, but the evidence is not conclusive, and additional factors, such as ocean conditions or competitive interactions with other species of salmon, may also be responsible. Regardless of the cause, these wide-spread phenotypic shifts influence fecundity and population abundance, and ultimately may put populations and associated fisheries at risk of decline.
The extent to which stray, hatchery-reared salmon affect wild populations is much debated. Although experiments show that artificial breeding and culture influence the genetics of hatchery salmon, little is known about the interaction between hatchery and wild salmon in a natural setting. Here, we estimated historical and contemporary genetic population structures of chum salmon (Oncorhynchus keta) in Prince William Sound (PWS), Alaska, with 135 single nucleotide polymorphism (SNP) markers. Historical population structure was inferred from the analysis of DNA from fish scales, which had been archived since the late 1960’s for several populations in PWS. Parallel analyses with microsatellites and a test based on Hardy-Weinberg proportions showed that about 50% of the fish-scale DNA was cross-contaminated with DNA from other fish. These samples were removed from the analysis. We used a novel application of the classical source-sink model to compare SNP allele frequencies in these archived fish-scales (1964–1982) with frequencies in contemporary samples (2008–2010) and found a temporal shift toward hatchery allele frequencies in some wild populations. Other populations showed markedly less introgression, despite moderate amounts of hatchery straying. The extent of introgression may reflect similarities in spawning time and life-history traits between hatchery and wild fish, or the degree that hybrids return to a natal spawning area. The source-sink model is a powerful means of detecting low levels of introgression over several generations.
Declines in populations of Pacific salmon Oncorhynchus spp. have been most pronounced in the southern extent of their range, and numerous anthropogenic stressors and natural drivers have been identified as potential causes. Using a paleolimnological approach, we have reconstructed the natural variability in the population dynamics of endangered Snake River sockeye salmon O. nerka over approximately the past 1,370 years. The rearing habitat ecology of their main production system, Redfish Lake, Idaho was also assessed over the past 500 years. Siliceous algal remains (diatoms and chrysophytes), stable nitrogen isotope δ15N, cladoceran zooplankton subfossils, and other proxy indicators archived in dated lake sediment cores were employed in this analysis. The inferred natural salmon production was much higher than that recorded in fisheries escapement data. Unprecedented declines in Snake River sockeye salmon production and changes in rearing system ecology were inferred over the past 150 years. The early, negative influences of the Columbia River commercial salmon harvest (in the 1860s) and sustained interruption of migration access (1910‐1934) from hydroelectric damming were evident. Enhanced zooplanktivory, associated with nonnative stocking and possible expansion of kokanee (lacustrine sockeye salmon) beginning in the 1920s and 1930s, appear to have altered the forage base for juvenile sockeye salmon, probably contributing to further declines. Lake nutrient enrichment since the 1950s was inferred, which changed nursery lake nutrient and trophic dynamics. This study highlights both site‐specific and regional influences on declines in past Snake River sockeye salmon population abundance and changes in rearing system ecology for these fish over the past 150 years. Such a long‐term ecological perspective is important to the continued conservation and management of this endangered species and has broader applications for other sockeye salmon runs at risk throughout their range.
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