Biogeographic Structure and Mitonuclear Discordance Reveal Cryptic Diversity in Pacific Herring ( <i>Clupea pallasii</i> )

Forage fishes are biological drivers throughout the Pacific Ocean, from the Arctic to nearly subtropical latitudes. As a critical trophic link, the health and stability of Pacific herring (<i>Clupea pallasii</i>) populations have implications for other marine species, including several targeted by large, productive fisheries. Previous research has indicated marked divergence between Pacific herring in the Bering Sea and the Gulf of Alaska. Seeking to localize this biogeographic break, we generated low-coverage whole genome resequencing data for 120 Pacific herring from seven sites across the northern Gulf of Alaska and the eastern Bering Sea and Aleutian Islands. Single nucleotide polymorphisms across the mitogenome (267) and nuclear genome (~5.6 million) corroborate a biogeographic break in Pacific herring along the Alaska Peninsula and Aleutian Islands, as far west as Unalaska. We identified two distinct populations: one exists along the northern coasts of the Aleutian Islands and in the eastern Bering Sea; the other occupies the southern edge of the Aleutians and the Gulf of Alaska. Two mitochondrial haplogroups co-occurring across the Gulf of Alaska suggest secondary contact between two populations, likely representing glacial refugia. Our results underscore the importance of geological events to contextualize the diversification of forage fish species.

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Publication Details

Journal
Ecology and Evolution
Published
2025-11-01
DOI
https://doi.org/10.1002/ece3.72452
Citations
2
Primary Topic
Genetic diversity and population structure
Type
article
Field-Weighted Citation Impact
3.63

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article

Biogeographic Structure and Mitonuclear Discordance Reveal Cryptic Diversity in Pacific Herring ( Clupea pallasii )

Laura E. Timm, Jessica R. Glass, J. Andrés López, Sydney A. Almgren
2 citations
Ecology and Evolution
Genetic diversity and population structure
3.63
article

Biogeographic Structure and Mitonuclear Discordance Reveal Cryptic Diversity in Pacific Herring ( Clupea pallasii )

Laura E. Timm, Jessica R. Glass, J. Andrés López, Sydney A. Almgren
article en
2 citations

Abstract

Forage fishes are biological drivers throughout the Pacific Ocean, from the Arctic to nearly subtropical latitudes. As a critical trophic link, the health and stability of Pacific herring (<i>Clupea pallasii</i>) populations have implications for other marine species, including several targeted by large, productive fisheries. Previous research has indicated marked divergence between Pacific herring in the Bering Sea and the Gulf of Alaska. Seeking to localize this biogeographic break, we generated low-coverage whole genome resequencing data for 120 Pacific herring from seven sites across the northern Gulf of Alaska and the eastern Bering Sea and Aleutian Islands. Single nucleotide polymorphisms across the mitogenome (267) and nuclear genome (~5.6 million) corroborate a biogeographic break in Pacific herring along the Alaska Peninsula and Aleutian Islands, as far west as Unalaska. We identified two distinct populations: one exists along the northern coasts of the Aleutian Islands and in the eastern Bering Sea; the other occupies the southern edge of the Aleutians and the Gulf of Alaska. Two mitochondrial haplogroups co-occurring across the Gulf of Alaska suggest secondary contact between two populations, likely representing glacial refugia. Our results underscore the importance of geological events to contextualize the diversification of forage fish species.

Ecology and EvolutionVol. 15(11)
National Oceanic and Atmospheric Administration (US), University of Alaska Fairbanks (US), NOAA National Marine Fisheries Service Alaska Fisheries Science Center (US), NOAA National Marine Fisheries Service Northwest Fisheries Science Center (US)
Massachusetts Department of Fish and Game, Alaska Department of Fish and Game, Purdue Climate Change Research Center, Purdue University
Openalex Percentile: Top 6%
Genetic diversity and population structure
3.63
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