| Autor: |
Chad J. Penn, Mark R. Williams, James Camberato, Nicholas Wenos, Hope Wason |
| Jazyk: |
angličtina |
| Rok vydání: |
2022 |
| Předmět: |
|
| Zdroj: |
Soil Systems, Vol 6, Iss 1, p 6 (2022) |
| Druh dokumentu: |
article |
| ISSN: |
2571-8789 |
| DOI: |
10.3390/soilsystems6010006 |
| Popis: |
Soil phosphorus (P) solubility and kinetics partly control dissolved P losses to surface water and uptake by plants. While previous studies have focused on batch techniques for measuring soil P desorption kinetics, flow-through techniques are more realistic because they simulate P removal from the system, akin to runoff, leaching, and plant uptake. The objectives were to measure soil P desorption by a flow-through technique at two flow rates and several batch methods, and utilize both for understanding how flow rate impacts the thermodynamics and kinetics of soil P desorption. Desorption obeyed first-order kinetics in two different phases: an initial rapid desorption phase followed by a gradual release. Desorption was limited by equilibrium and the kinetics of physical processes as demonstrated by an interruption test. Dilution-promoted desorption occurred with increasing cumulative volume, which increased desorption rate via first-order kinetics. The batch tests that simulated cumulative solution volume and time of flow-through were similar to the flow-through results; however, the batch methods overestimated the desorption rates due to less limitations to diffusion. Fast flow rates desorbed less P, but at a greater speed than slow flow rates. The differences were due to contact time, cumulative time, and solution volume, which ultimately controlled the potential for chemical reactions to be realized through physical processes. The interaction between these processes will control the quantity and rate of desorption that buffer P in non-point drainage losses and plant uptake. |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
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