4.5 Article

Chemical speciation of iron in the euphotic zone along the Kuroshio Current

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MARINE CHEMISTRY
卷 233, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.marchem.2021.103966

关键词

Iron; Ligands; Kuroshio; East China Sea

资金

  1. JSPS KAKENHI [JP18H03361, JP26241009, JP24121006, JP15H05820, JP15H05817]

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The study revealed differences in the distributions of DFe and L-Fe between the Kuroshio Current and its neighboring waters, with unique characteristics observed in the surface waters of the Kuroshio. The neighboring waters were classified into two types: East China Sea water and coastal water, each with distinct vertical gradients of DFe concentration. These findings suggest that different processes contribute to the iron dynamics in the Kuroshio area and its surrounding waters.
The distributions of dissolved iron (DFe) and organic iron-binding ligands (L-Fe) in the Kuroshio Current and its neighboring waters were elucidated from four cross-sectional surveys from the eastern coast of Taiwan to Sagami Bay. The Kuroshio surface water was characterized by a high salinity, low concentration of DFe, high concentration of L-Fe, and low fluorescence of humic-like substances, in comparison to the neighboring waters. The neighboring waters of the Kuroshio can be categorized into two types: the East China Sea water and coastal water. The East China Sea water was found near the Okinawa Trough, and characterized by a steep vertical gradient of DFe concentration, almost as low as that in the Kuroshio within the surface mixed layer, but reached similar to 0.5 nM below the mixed layer. Coastal water was observed on the southern coast of Japan, and its DFe concentration was high throughout the upper 200 m. The concentration of L-Fe in the Kuroshio water was significantly higher at 10-m depth than in the deeper layers. This suggests that humic-like substances, which are a major component of L-Fe in estuarine and deep waters, play a relatively minor role in the Kuroshio surface waters. Mixing with coastal waters can increase the concentration of bioavailable inorganic ferric ions in the Kuroshio surface water in two ways, by increasing the DFe concentration and decreasing the L-Fe concentration.

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