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Published on: June 4, 2021
Effects of elevated atmospheric CO2 on dissolution of geological fluorapatite in water and soil
1College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing, Jiangsu 210095, China; State Key Laboratory for Mineral Deposits Research, Nanjing University, Nanjing, Jiangsu 210046, China; Jiangsu Provincial Key Lab for Organic Solid Waste Utilization, Nanjing Agricultural University, Nanjing, 210095, China.
Abstract:
Most of phosphorus (P) is present as insoluble phosphorus-bearing minerals or organic forms in soil. Geological fluorapatite (FAp) is the dominant mineral-weathering source of P. In this study, FAp was added into water and soil under elevated CO2 to investigate the pathway of P release. Two types of soils (an acidic soil from subtropical China and a saline-alkali soil from Tibet Plateau, China) with similar total P content were studied. In the solution, increased CO2 in air enhanced the dissolution of FAp, i.e., from 0.04 to 1.18ppm for P and from 2.48 to 13.61ppm for Ca. In addition, release of Ca and P from FAp reached the maximum (2.14ppm for P and 13.84ppm for Ca) under the combination of elevated CO2 and NaCl due to the increasing ion exchange. Consistent with the results from the solution, CO2 elevation promoted P release more significantly (triple) in the saline-alkali soil than in the acidic soil. Therefore, saline-alkali soils in Tibet Plateau would be an important reservoir of available P under the global CO2 rise. This study sheds the light on understanding the geological cycle of phosphorus.
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