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Nanoplastics induce epigenetic signatures of transgenerational impairments associated with reproduction in copepods under ocean acidification

Journal of Hazardous Materials 2023 38 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count.
Young Hwan Lee, Min‐Sub Kim, Yoseop Lee, Duck‐Hyun Kim, Jae‐Seong Lee

Summary

This study examined how nanoplastics combined with ocean acidification affect tiny marine crustaceans called copepods across ten generations. Researchers found that the two stressors together caused synergistic harm to reproduction, with effects passed down to future generations through epigenetic changes in DNA. The findings suggest that climate change and plastic pollution may interact to create lasting, inherited damage in marine organisms.

Body Systems
Study Type Environmental

Ocean acidification (OA) is one of many major global climate changes that pose a variety of risks to marine ecosystems in different ways. Meanwhile, there is growing concern about how nanoplastics (NPs) affect marine ecosystems. Combined exposure of marine organisms to OA and NPs is inevitable, but their interactive effects remain poorly understood. In this study, we investigated the multi- and transgenerational toxicity of NPs on copepods under OA conditions for ten generations. The findings revealed that OA and NPs have a synergistic negative effect on copepod reproduction across generations. In particular, the transgenerational groups showed reproductive impairments in the F1 and F2 generations (F1T and F2T), even though they were never exposed to NPs. Moreover, our epigenetic examinations demonstrated that the observed intergenerational reproductive impairments are associated with differential methylation patterns of specific genes, suggesting that the interaction of OA and NPs can pose a significant threat to the sustainability of copepod populations through epigenetic modifications. Overall, our findings provide valuable insight into the intergenerational toxicity and underlying molecular mechanisms of responses to NPs under OA conditions.

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