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Migration is essential for the reproduction and survival of many animals, yet little is understood about its underlying molecular mechanisms. We used the salmonid Oncorhynchus mykiss to gain mechanistic insight into smoltification, which is a morphological, physiological, and behavioral transition undertaken by juveniles in preparation for seaward migration. O. mykiss is experimentally tractable and displays intra- and inter-population variation in migration propensity. Migratory individuals can produce non-migratory progeny and vice versa, indicating a high degree of phenotypic plasticity. One potential way that phenotypic plasticity might be linked to variation in migration-related life history tactics is through epigenetic regulation of gene expression. To explore this, we quantitatively measured genome-scale DNA methylation in fin tissue using reduced representation bisulfite sequencing of F2 siblings produced from a cross between steelhead (migratory) and rainbow trout (non-migratory) lines. We identified 57 differentially methylated regions (DMRs) between smolt and resident O. mykiss juveniles. DMRs were high in magnitude, with up to 62% differential methylation between life history types, and over half of the gene-associated DMRs were in transcriptional regulatory regions. Many of the DMRs encode proteins with activity relevant to migration-related transitions (e.g. circadian rhythm pathway, nervous system development, protein kinase activity). This study provides the first evidence of a relationship between epigenetic variation and life history divergence associated with migration-related traits in any species.

Thermal exposure is a serious and growing challenge facing fish species worldwide. Chinook salmon (Oncorhynchus tshawytscha) living in the southern portion of their native range are particularly likely to encounter warmer water due to a confluence of factors. River alterations have increased the likelihood that juveniles will be exposed to warm water temperatures during their freshwater life stage, which can negatively impact survival, growth, and development and pose a threat to dwindling salmon populations. To better understand how acute thermal exposure affects the biology of salmon, we performed a transcriptional analysis of gill tissue from Chinook salmon juveniles reared at 12° and exposed acutely to water temperatures ranging from ideal to potentially lethal (12° to 25°). Reverse-transcribed RNA libraries were sequenced on the Illumina HiSeq2000 platform and a de novo reference transcriptome was created. Differentially expressed transcripts were annotated using Blast2GO and relevant gene clusters were identified. In addition to a high degree of downregulation of a wide range of genes, we found upregulation of genes involved in protein folding/rescue, protein degradation, cell death, oxidative stress, metabolism, inflammation/immunity, transcription/translation, ion transport, cell cycle/growth, cell signaling, cellular trafficking, and structure/cytoskeleton. These results demonstrate the complex multi-modal cellular response to thermal stress in juvenile salmon.

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The Sacramento splittail is an endemic cyprinid fish of the San Francisco estuary and its tributaries, which is a highly manipulated, constantly changing ecosystem. Splittail is the only extant member of its genus and is listed as a federal and California Species of Special Concern due to uncertainties regarding long-term abundance trends. Determining population structure for splittail is important because unique populations may contain different adaptive genetic variation, which can allow one population to persist through future environmental or demographic stochasticity while others become extirpated. To assess splittail population structure, 13 microsatellite markers were used to genotype 489 young-of-year splittail from five major rivers draining into the estuary: Cosumnes, Napa, Petaluma, Sacramento, and San Joaquin Rivers. Two genetically distinct populations were found to exist within our study region; one largely comprised of splittail collected from the Petaluma and Napa Rivers and the second comprised of splittail collected from tributaries in California's Central Valley: Cosumnes, Sacramento, and San Joaquin Rivers. These results were replicated in two consecutive years with both distance and model-based algorithms. The genetic distinction between these two populations appears correlated with salinity differences between migratory regions and spawning grounds. Splittail from the Petaluma River exhibited a significantly higher degree of differentiation from the Central Valley population than did Napa River splittail. Our results suggest ongoing monitoring programs are probably highly biased towards sampling splittail from the Central Valley population. Understanding population dynamics of splittail could be improved if monitoring programs were expanded to include all splittail populations.

Accurate species identification is essential for ecological research and environmental monitoring. Some species are easy to identify visually, while identification of others is more challenging due to cryptic speciation (Hubert et al., 2008) and phenotypic plasticity (Pinzón et al., 2013). In these cases, as well as for more refined taxonomic discrimination (e.g., populations), genetic methods are often considerably more accurate (Benjamin et al., 2018; Vrijenhoek, 2009). To date, genetic identification has required a trained geneticist to receive the sample, conduct molecular methods (usually in a laboratory), analyse results and report the findings back to their field collaborators. This process can require days, and possibly even months, thus delaying the progression of research, conservation, and management actions based on the findings. In addition, laboratory facilities may not be available for genetic species identification

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