Lauriane Vilmin, Alexander F. Bouwman, Arthur H. W. Beusen, Wim Joost van Hoek, José M. Mogollón
{"title":"Past anthropogenic activities offset dissolved inorganic phosphorus retention in the Mississippi River basin","authors":"Lauriane Vilmin, Alexander F. Bouwman, Arthur H. W. Beusen, Wim Joost van Hoek, José M. Mogollón","doi":"10.1007/s10533-022-00973-1","DOIUrl":null,"url":null,"abstract":"<div><p>The rapid acceleration of anthropogenic phosphorus (P) loadings to watersheds has fuelled massive freshwater and coastal eutrophication and completely changed the global P cycle. Within watersheds, emitted P is transported downstream towards estuaries. Reservoirs can retain a significant proportion of this P. In the long term, this accumulated P can however be re-mobilized, a process lacking in current global P budgets. Here, we include P cycling in a coupled integrated assessment-hydrology-biogeochemistry framework with 0.5 by 0.5-degree spatial resolution and an annual time resolution, and apply it to the Mississippi River basin (MRB). We show that, while reservoirs have aided in the net retention of P, they serve as dissolved inorganic P (DIP) sources due to the transformation of legacy P in sediments. The increasing DIP sourcing in the MRB has been offsetting P retention in streams, especially towards the end of the twentieth century. Due to its bioavailability, DIP is the most likely form to trigger eutrophication. Although P inputs into the MRB have decreased since the 1970s, legacy effects are delaying positive outcomes of remediation measures.</p></div>","PeriodicalId":8901,"journal":{"name":"Biogeochemistry","volume":"161 2","pages":"157 - 169"},"PeriodicalIF":3.9000,"publicationDate":"2022-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10533-022-00973-1.pdf","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biogeochemistry","FirstCategoryId":"93","ListUrlMain":"https://link.springer.com/article/10.1007/s10533-022-00973-1","RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 2
Abstract
The rapid acceleration of anthropogenic phosphorus (P) loadings to watersheds has fuelled massive freshwater and coastal eutrophication and completely changed the global P cycle. Within watersheds, emitted P is transported downstream towards estuaries. Reservoirs can retain a significant proportion of this P. In the long term, this accumulated P can however be re-mobilized, a process lacking in current global P budgets. Here, we include P cycling in a coupled integrated assessment-hydrology-biogeochemistry framework with 0.5 by 0.5-degree spatial resolution and an annual time resolution, and apply it to the Mississippi River basin (MRB). We show that, while reservoirs have aided in the net retention of P, they serve as dissolved inorganic P (DIP) sources due to the transformation of legacy P in sediments. The increasing DIP sourcing in the MRB has been offsetting P retention in streams, especially towards the end of the twentieth century. Due to its bioavailability, DIP is the most likely form to trigger eutrophication. Although P inputs into the MRB have decreased since the 1970s, legacy effects are delaying positive outcomes of remediation measures.
期刊介绍:
Biogeochemistry publishes original and synthetic papers dealing with biotic controls on the chemistry of the environment, or with the geochemical control of the structure and function of ecosystems. Cycles are considered, either of individual elements or of specific classes of natural or anthropogenic compounds in ecosystems. Particular emphasis is given to coupled interactions of element cycles. The journal spans from the molecular to global scales to elucidate the mechanisms driving patterns in biogeochemical cycles through space and time. Studies on both natural and artificial ecosystems are published when they contribute to a general understanding of biogeochemistry.