Abstract

AbstractSpatial distributions of dimethylsulfide (DMS), dimethylsulfoniopropionate (DMSP), and dimethyl sulfoxide (DMSO) in the northern South China Sea were determined in the summer of 2015. The mean concentrations of DMS, particulate DMSP (DMSPp), dissolved DMSP (DMSPd), dissolved DMSO (DMSOd), and particulate DMSO (DMSOp) in the surface seawater were 2.8 ± 1.0, 6.8 ± 1.5, 14.0 ± 3.1, 12.2 ± 3.2, and 9.2 ± 2.6 nmol L−1, respectively. The contributions of three principal removal pathways of DMS were investigated. The average biological production and consumption rates of DMS in the surface seawater were 6.15 ± 1.12 and 4.63 ± 1.32 nmol L−1 day−1. Deck incubation experiments showed that the photooxidation rates of DMS for different radiation bands followed the order: KUVB > KUVA > Kvisible light. The DMS photooxidation rates were higher in the coastal waters than in the open ocean, which might be associated with the higher concentrations of dissolved organic matter of terrigenous input. The sea‐to‐air fluxes of DMS ranged from 1.6 to 50.3 μmol m−2 day−1 with an average value of 15.6 ± 11.6 μmol m−2 day−1. Based on the respective turnover times of DMS, the contributions of biological consumption, photooxidation, and sea‐to‐air exchange to the sink of DMS were 32.6 ± 11.0%, 23.2 ± 8.9%, and 44.1 ± 19.2%, respectively, suggesting that the three removal pathways were all critical to the migration and transformation of DMS in the surface seawater during summer.

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