1 Introduction Geochemical mapping at national and continental scales continues to present challenges worldwide due to variations in geologic and geotectonic units.Use of the proper sampling media can provide rich inf...1 Introduction Geochemical mapping at national and continental scales continues to present challenges worldwide due to variations in geologic and geotectonic units.Use of the proper sampling media can provide rich information on展开更多
Dissolved selenium in the Changjiang（Yangtze） Estuary and its adjacent waters was determined by hydride generation atomic fluorescence spectrometry to elucidate the source, behavior in estuary, adsorption-desorption...Dissolved selenium in the Changjiang（Yangtze） Estuary and its adjacent waters was determined by hydride generation atomic fluorescence spectrometry to elucidate the source, behavior in estuary, adsorption-desorption process and biological role. In surface water, Se（IV） concentration ranged 0.05–1.14 nmol/L and Se（VI） concentration varied 0.01–1.20 nmol/L, with the means of 0.76 and 0.49 nmol/L, respectively. In bottom water, Se（IV） content varied 0.03–0.27 nmol/L and Se（VI） content ranged 0.04–0.85 nmol/L, with the averages of 0.10 and 0.40 nmol/L, respectively. High level of Se（IV） was observed near the shore with a significant decrease towards the open sea, suggesting the continental input from the adjacent rivers. Large value of Se（VI） was found in bottom water, reflecting the release from suspended sediment. Besides, high value appeared in the same latitude of the Changjiang Estuary and Hangzhou Bay illustrated the effect of lateral mixing and the long-distance transport of selenium. Se（VI）, more soluble, occupied higher percentage in aqueous environment. The presence of Se（IV） resulted from the degradation of residue and the reduction of Se（VI） under anaerobic condition. The positive relationship to suspended particulate material（SPM） and negative correlation to depth indicated that Se（IV） tended to be released from the high density particulate matter. Instead, Se（VI） content did not significantly relate to SPM since it generally formed inner-sphere complex to iron hydroxide. Se（IV） content negatively varied to salinity and largely depended on the freshwater dilution and physical mixing. While, Se（VI） level deviated from the dilution line due to the in situ biogeochemical process such as removal via phytoplankton uptake and inputs via organic matter regeneration. As the essential element, Se（IV） was confirmed more bioavailable to phytoplankton growth than Se（VI）, and moreover, seemed to be more related to phosphorus than to nitrogen.展开更多
基金supported by the Special Scientific Research Fund of Public Welfare Profession of Ministry of Land and Resources of the People’s Republic of China (No. 201011057)
文摘1 Introduction Geochemical mapping at national and continental scales continues to present challenges worldwide due to variations in geologic and geotectonic units.Use of the proper sampling media can provide rich information on
基金The National Natural Science Foundation of China for Creative Research Groups under contract No.41121064the National Natural Science Foundation of China under contract No.41306055+1 种基金the Strategic Priority Research Program of the Chinese Academy of Sciences under contract No.XDA05030402the National Basic Research Program of China(973 Program)under contract No.2011CB403602
文摘Dissolved selenium in the Changjiang（Yangtze） Estuary and its adjacent waters was determined by hydride generation atomic fluorescence spectrometry to elucidate the source, behavior in estuary, adsorption-desorption process and biological role. In surface water, Se（IV） concentration ranged 0.05–1.14 nmol/L and Se（VI） concentration varied 0.01–1.20 nmol/L, with the means of 0.76 and 0.49 nmol/L, respectively. In bottom water, Se（IV） content varied 0.03–0.27 nmol/L and Se（VI） content ranged 0.04–0.85 nmol/L, with the averages of 0.10 and 0.40 nmol/L, respectively. High level of Se（IV） was observed near the shore with a significant decrease towards the open sea, suggesting the continental input from the adjacent rivers. Large value of Se（VI） was found in bottom water, reflecting the release from suspended sediment. Besides, high value appeared in the same latitude of the Changjiang Estuary and Hangzhou Bay illustrated the effect of lateral mixing and the long-distance transport of selenium. Se（VI）, more soluble, occupied higher percentage in aqueous environment. The presence of Se（IV） resulted from the degradation of residue and the reduction of Se（VI） under anaerobic condition. The positive relationship to suspended particulate material（SPM） and negative correlation to depth indicated that Se（IV） tended to be released from the high density particulate matter. Instead, Se（VI） content did not significantly relate to SPM since it generally formed inner-sphere complex to iron hydroxide. Se（IV） content negatively varied to salinity and largely depended on the freshwater dilution and physical mixing. While, Se（VI） level deviated from the dilution line due to the in situ biogeochemical process such as removal via phytoplankton uptake and inputs via organic matter regeneration. As the essential element, Se（IV） was confirmed more bioavailable to phytoplankton growth than Se（VI）, and moreover, seemed to be more related to phosphorus than to nitrogen.
