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Wet deposition of phosphorus in Florida
Institution:1. Social, Economic and Geographical Sciences Group, United Kingdom;2. Environmental and Biochemical Sciences Group, United Kingdom;3. Information and Computational Sciences, James Hutton Institute, Craigiebuckler, Aberdeen AB15 8QH, United Kingdom;4. Norsk Institutt for Vannforskning (NIVA), Gaustadalléen 21, 0349, Oslo, Norway;1. Key Laboratory of Poyang Lake Environment and Resource Utilization, Ministry of Education, School of Resource and Environment, Nanchang University, Nanchang 330031, China;2. School of Materials and Chemical Engineering, Pingxiang University, Pingxiang 337000, China
Abstract:Wet deposition of phosphorus was measured at 10 sites across Florida originally established as part of the Florida Atmospheric Mercury Study conducted between 1992 and 1996. Monthly integrated samples were collected and analyzed using a total analytical protocol that incorporated “clean lab” conditions for sample equipment preparation and Aerochem Metrics collectors modified for suitability to use for ultra-trace elements. Samples also were collected aboard 15 m towers to minimize any influence on measured deposition by insects, etc., and locally originating particles that do not contribute to true net deposition. Extensive replication of samples in the field was conducted (ca. 83%). The average absolute difference between replicates was 16.2%, with a median absolute difference of 9.5%. Replicate precision was poorest for concentrations above 0.080 mg P l?1, suggesting that concentrations above this level are contaminated.The wet deposition concentrations and fluxes of phosphorus measured in this study are appreciably lower than those reported by previous investigators for wet deposition in Florida, and lie at the lower end of measurements reported in the recent literature. For example, the volume weighted mean concentration and flux for wet deposition across all our study sites averaged 0.005 mg P l?1 and 7.5 mg P m?2 yr?1, respectively, which is approximately 50% and 32% lower than that reported by Hendry et al. (1981 in Atmospheric Pollutants in Natural Waters. Ann Arbor Science, Ann Arbor. MI, pp. 199–215). Our lower measurements likely reflect three factors: (1) the ultra-trace element sampling and analytical protocols; (2) improved collector design to eliminate sampling artifacts (e.g., splash-off contamination and transfer of contaminants from the dry bucket); and (3) placement of collectors off the ground surface. Lower VWM concentrations were observed near the Florida coast; otherwise, strong spatial patterns across the state were absent. Seasonal variations in VWM also were not pronounced, although deposition fluxes were highest during the summer wet season in response to the strong seasonal distribution of rainfall.
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