Search

Understanding the conservation status of native fish populations is increasingly important because they are put at risk by mounting anthropogenic pressures, including climate change. Conventional approaches to assess fish populations can be logistically challenging and cost-prohibitive. As a result, resource managers often make assumptions about the status of fish populations based on limited information. The watersheds of Washington’s San Juan Islands were considered too small to support wild salmonid populations. Many streams flow only seasonally, and all have been subjected to varying degrees of anthropogenic impacts affecting their ecological integrity. Nonetheless, we found that at least five watersheds in the archipelago support populations of coastal cutthroat trout (Oncorhynchus clarki clarki). To better understand the conservation status of coastal cutthroat trout populations there, we genotyped approximately fifty trout in each of three watersheds: Cascade and Doe Bay creeks on Orcas Island and Garrison Creek on San Juan Island. Results suggest that two watersheds support native populations and one supports naturalized hatchery fish. The likely native coastal cutthroat trout diversity documented in the two watersheds contributes to the overall diversity of the species, demonstrates that species’ resiliency, and provides justification for conservation measures. Effective management and conservation planning in data-limited situations requires the use of a precautionary approach. Population genetics provide a useful tool for identifying vulnerable fish populations and understanding their relationships with other conspecific populations. This information can inform restoration goals and help identify and prioritize restoration and protection measures.

Technological advancements have allowed geneticists to exploit an increasing array of molecular markers, many of which have different properties and may provide contrasting insights into the evolutionary history and structure of populations. This has important consequences for conservation managers attempting to identify units at which to conserve intraspecific diversity. In this study we compared the inferences derived from nuclear microsatellites and restriction-site associated DNA (RADseq) data for a threatened freshwater fish, the bull trout Salvelinus confluentus. For both marker types we generated data for the same suite of individuals collected from 24 populations distributed across the species range. The RADseq data were low coverage (mean site coverage

Programs to rebuild imperiled wild fish populations often include hatchery-born fish derived from wild populations to supplement natural spawner abundance. These programs require monitoring to determine their demographic, biological, and genetic effects. In 1990s in Washington State, the Summer Chum Salmon Conservation Initiative developed a recovery program for the threatened Hood Canal summer chum salmon Evolutionarily Significant Unit (ESU) (the metapopulation) that used in-river spawners (wild fish) for each respective supplementation broodstock in six tributaries. Returning spawners (wild-born and hatchery-born) composed subsequent broodstocks, and tributary-specific supplementation was limited to three generations. We assessed impacts of the programs on neutral genetic diversity in this metapopulation using 16 microsatellite loci and a thirty-year dataset spanning before and after supplementation, roughly eight generations. Following supplementation, differentiation among subpopulations decreased (but not significantly) and isolation by distance patterns remained unchanged. There was no decline in genetic diversity in wild-born fish, but hatchery-born fish sampled in the same spawning areas had significantly lower genetic diversity and unequal family representation. Despite potential for negative effects from supplementation programs, few were detected in wild-born fish. We hypothesize that chum salmon natural history makes them less vulnerable to negative impacts from hatchery supplementation.

We demonstrate an efficient model for standardizing microsatellite DNA data among laboratories studying Oncorhynchus mykiss. Eight laboratories standardized 13 microsatellite loci following allele nomenclature of a central laboratory (average inter-laboratory genotyping concordance >98%). Following this central model, we have currently standardized 298 alleles from throughout the species native range. Although we focus here on O. mykiss, our experiences and recommendation apply equally to other broadly distributed species that may benefit from multi-laboratory collaborative data collection.

The lower Columbia River drainage once supported a run of over a million chum salmon. By the late 1950s, the run had decreased to often a few hundred fish. With the exception of Grays River near the coast and an aggregation of chum salmon spawning in creeks and the main stem near Bonneville Dam in the Columbia Gorge, most populations were thought to be extinct. However, chum salmon consistently return in low numbers to tributaries originating in the Cascade Range: the Cowlitz, Lewis, and Washougal rivers. To assess whether Cascade spawners were strays or remnants of former populations, chum salmon from the Coastal, Cascade and Gorge ecoregional zones were characterized at 17 microsatellite loci. Significant heterogeneity in genotype distributions was detected between zones and collections formed regional groups in a neighbor-joining tree. Cascade collections had higher allelic richness and private alleles, and the Cowlitz River supported genetically divergent fall and summer runs, the only summer chum salmon run extant in the Columbia River drainage. We propose that chum salmon in the Cascade zone are remnants of original populations. We attribute the divergence between zonal groups to diverse ecological conditions in each zone, which promoted regional genetic adaptation, and to genetic drift experienced in small populations.

For over a century, Washington State Department of Fish and Wildlife has implemented hatchery programs as a means to boost salmon abundance. Concerns have developed that native populations may be replaced by hatchery strains, decreasing the genetic diversity required to respond to environmental changes. We report a comparison of microsatellite DNA variation in wild-spawning and hatchery-strain coho salmon from the Nooksack and Samish rivers in northern Puget Sound. Significant heterogeneity in genotype frequencies was detected between wild-spawning coho salmon from the upper North Fork (NF) Nooksack River and hatchery-strain coho salmon from the Nooksack River (descendants of primarily Nooksack River broodstock). Little difference in genotype frequencies was detected between wild-spawning coho salmon from the Samish River and hatchery-strain coho salmon from the Nooksack River. The 13-locus suite provided high resolution: in assignment tests over 85% of wild-spawning coho salmon from the upper NF Nooksack River were assigned to source. Wild-spawning coho salmon collected below hatcheries in the Nooksack River and 50% of wild-spawning Samish River coho salmon were assigned to hatchery collections. The genetic divergence of wild-spawning coho salmon in the upper NF Nooksack River is remarkable given the extensive stocking history and proximity of a hatchery. We suggest that these upper river fish are native coho salmon and that wild spawners in the lower Nooksack and Samish River are descendants of hatchery productions. We attribute divergence to earlier run timing in upper NF Nooksack River wild spawners, availability of extensive spawning and rearing habitat upstream of a hatchery in the upper NF Nooksack River, and a longer stocking history in the Samish River.

Snails of the Littorina saxatilis species complex are ubiquitous and important members of hard shore intertidal communities in the North Atlantic. The complex includes L. arcana, L. compressa and L. saxatilis. We investigated species and population structure among these species from six locations in Ireland and Britain using a nonradioactive single strand conformational polymorphism analysis of a 375 base pair fragment of the cytochrome-b gene. Variability was high with 38 haplotypes found in 591 individuals. The most common haplotype in L. arcana and L. compressa was absent from L. saxatilis and the most common haplotype in L. saxatilis was found in low numbers in L. arcana and L. compressa. Haplotypes restricted to L. arcana and L. compressa formed a cluster separate from L. saxatilis haplotypes in maximum parsimony and multidimensional scaling analyses. In analyses examining populations, L. arcana and L. compressa formed a group separate from L. saxatilis. Both the populations in the L. arcana/L. compressa group and in L. saxatilis show similar geographical structuring in that the North England populations were separated from a cluster of Cornwall (South-west England) and Irish populations. We suggested that Pleistocene sea level changes accounted for these congruent genetic patterns. We concluded that L. arcana and L. compressa are more closely related to each other than either is to L. saxatilis and offer this as a resolution to a previous trichotomy.