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Global Biogeochemical Cycle of Fluorine
Author(s) -
Schlesinger William H.,
Klein Emily M.,
Vengosh Avner
Publication year - 2020
Publication title -
global biogeochemical cycles
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.512
H-Index - 187
eISSN - 1944-9224
pISSN - 0886-6236
DOI - 10.1029/2020gb006722
Subject(s) - biogeochemical cycle , weathering , authigenic , geochemical cycle , terrigenous sediment , groundwater , context (archaeology) , biogeochemistry , environmental chemistry , seawater , geology , surface water , environmental science , geochemistry , earth science , sedimentary rock , oceanography , chemistry , environmental engineering , paleontology , geotechnical engineering
This review provides a synthesis of what is currently known about the natural and anthropogenic fluxes of fluorine on Earth, offering context for an evaluation of the growing environmental impact of human‐induced F mobilization and use. The largest flux of F at the Earth's surface derives from the mobilization of F during chemical (2.2 Tg F/yr (where 1 Tg = 10 12 g) and mechanical (7 Tg F/yr) weathering of rocks. Humans supplement these fluxes by mining fluorospar and apatite ores to make a variety of industrial chemicals and fertilizers, mobilizing 2.9 and 7.6 Tg F/yr, respectively. Other large anthropogenic fluxes derive from the manufacture of bricks (1.8 Tg F/yr) and extraction of groundwater (0.9 to 1.7 Tg F/yr). Rivers deliver ~3.6 Tg/yr of dissolved fluoride to the oceans, where the mean residence time of dissolved F in seawater is ~500,000 yr. F is removed from the oceans by the deposition of terrigenous (4.3 Tg F/yr) and authigenic sediments (1.24 Tg F/yr), and approximately 10 Tg F/yr is removed from the surface of the Earth by subduction of the oceanic lithosphere. Humans have increased the flux of F to the atmosphere and in rivers by more than a factor of 2, with the largest impacts stemming from the use of phosphorus fertilizers, the production of brick, and extraction of groundwater. Despite their well‐documented toxicity, perfluoroalkyl substances make only a small contribution to F emitted to the atmosphere and natural waters.