| Literature DB >> 28013537 |
Hyunji Kim1, Anne L Soerensen2, Jin Hur3, Lars-Eric Heimbürger4, Doshik Hahm5, Tae Siek Rhee6, Seam Noh1, Seunghee Han1.
Abstract
Methylmercury (MeHg) accumulation in marine organisms poses serious ecosystem and human health risk, yet the sources of MeHg in the surface and subsurface ocean remain uncertain. Here, we report the first MeHg mass budgets for the Western Pacific Ocean estimated based on cruise observations. We found the major net source of MeHg in surface water to be vertical diffusion from the subsurface layer (1.8-12 nmol m-2 yr-1). A higher upward diffusion in the North Pacific (12 nmol m-2 yr-1) than in the Equatorial Pacific (1.8-5.7 nmol m-2 yr-1) caused elevated surface MeHg concentrations observed in the North Pacific. We furthermore found that the slope of the linear regression line for MeHg versus apparent oxygen utilization in the Equatorial Pacific was about 2-fold higher than that in the North Pacific. We suggest this could be explained by redistribution of surface water in the tropical convergence-divergence zone, supporting active organic carbon decomposition in the Equatorial Pacific Ocean. On the basis of this study, we predict oceanic regions with high organic carbon remineralization to have enhanced MeHg concentrations in both surface and subsurface waters.Entities:
Mesh:
Substances:
Year: 2017 PMID: 28013537 DOI: 10.1021/acs.est.6b04238
Source DB: PubMed Journal: Environ Sci Technol ISSN: 0013-936X Impact factor: 9.028