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Decreased Dimethylsulfide and Increased Polybrominated Methanes: Potential Climate Effects of Microplastic Pollution in Acidified Ocean
Summary
A ship-based microcosm experiment simulating ocean acidification and microplastic pollution found that combined conditions decreased dimethylsulfide production and increased polybrominated methane emissions, with potential climate-active gas implications for ocean carbon cycling.
Microplastic (MP) pollution and ocean acidification (OA) are pressing marine environmental concerns, but their combined impacts on short-lived biogenic climate-active gases and the resulting climate effects remain unclear. To address this gap, a ship-based microcosm experiment was conducted, where OA and MP pollution were simulated under in situ conditions to explore their effects on the production of dimethylsulfide (DMS), bromoform (CHBr3), and dibromomethane (CH2Br2). The results indicated that both MP and OA inhibited phytoplankton growth and DMS concentration, with OA inducing further reductions in the production rate and yield of DMS. MP addition led to extra dissolved organic matter, and the acidified condition enhanced bromoperoxidase activity, both of which promoted the production of CHBr3 and CH2Br2. When OA and MP addition were combined, DMS concentrations decreased by 61%, whereas CHBr3 and CH2Br2 concentrations increased by 132% and 45%, respectively. Based on the results, MP pollution under OA conditions might directly reduce DMS accumulation or decrease the formation of DMS-derived sulfate aerosols by increasing CHBr3 and CH2Br2 levels, which finally weaken DMS's climate-cooling capabilities. This study underscores the potential for MP pollution in future acidified oceans to exacerbate global warming by disrupting the cycle of marine biogenic climate-active gases.
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