Identifying dissolved reactive phosphorus sources in agricultural runoff and leachate using phosphate oxygen isotopes

Rose C.K. Mumbi, Mark R. Williams, William I. Ford, James J. Camberato, Chad J. Penn

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Agricultural phosphorus (P) losses may result from either recently applied fertilizers or from P accumulated in soil and sediment. While both P sources pose an environmental risk to freshwater systems, differentiating between sources is crucial for identifying and implementing management practices to decrease loss. In this study, laboratory rainfall simulations were completed on runoff boxes and undisturbed soil columns before and after fertilizer application. The oxygen-18 signature of phosphate (δ18OPO4) in fertilizer, surface runoff, subsurface leachate, and soil were analyzed (n = 107 samples) to quantify new (recently applied) and old (soil) P losses in runoff and leachate. Results showed that dissolved reactive P (DRP) concentration in runoff and leachate substantially increased during the rainfall simulation immediately after fertilizer application, with runoff and leachate δ18OPO4 similar to fertilizer δ18OPO4 signatures. Greater than 90 % of the DRP load during this event could be attributed to direct loss of P from fertilizer using δ18OPO4. Beyond the first rainfall event after fertilizer application, DRP concentration decreased and leachate δ18OPO4 values differed from the fertilizer values. Interpretation of isotope results was challenging because both abiotic (isotope fractionation during transport) and biotic (P cycling) processes may have influenced δ18OPO4 signatures during these subsequent events. While abiotic effects on δ18OPO4 appear more probable given the experimental conditions in the current study (high soil test P concentration, short duration between rainfall simulations, and strong relationship between event water and δ18OPO4 signature), tracing or separating P sources remains highly uncertain during these events post-fertilizer application. Findings highlight both potential opportunities and challenges of using δ18OPO4 to trace sources of P through the landscape.

Original languageEnglish
Article number104501
JournalJournal of Contaminant Hydrology
Volume269
DOIs
StatePublished - Feb 2025

Bibliographical note

Publisher Copyright:
© 2024

Funding

The authors would like to thank the landowner of the study site for his continued support for conducting research on his field. The authors would also like to thank the students and staff at the USDA ARS National Soil Erosion Research Laboratory for assistance with field and lab work. Research was partially supported by the National Science Foundation (Grant No.: 2032701). This research was also a contribution from the Conservation Effects Assessment Project (CEAP). CEAP is supported by the United States Department of Agriculture.

FundersFunder number
USDA ARS National Soil Erosion Research Laboratory
U.S. Department of Agriculture
NRCS Conservation Effects Assessment Project
National Science Foundation Arctic Social Science Program2032701

    Keywords

    • Dissolved reactive phosphorus
    • Phosphorus cycling
    • Stable isotopes
    • Tracer
    • Water quality

    ASJC Scopus subject areas

    • Environmental Chemistry
    • Water Science and Technology

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