Abstract
Phosphorus (P) is a limiting or co-limiting nutrient to plants and microorganisms in diverse ecosystems that include the arctic tundra. Certain soil minerals can adsorb or co-precipitate with phosphate, and this mineral-bound P provides a potentially large P reservoir in soils. Iron (Fe) oxyhydroxides have a high capacity to adsorb phosphate; however, the ability of Fe oxyhydroxides to adsorb phosphate and limit P bioavailability in organic tundra soils is not known. Here, we examined the depth distribution of soil Fe and P species in the active layer (<30 cm) of low-centered and high-centered ice-wedge polygons at the Barrow Environmental Observatory on the Alaska North Slope. Soil reservoirs of Fe and P in bulk horizons and in narrower depth increments were characterized using sequential chemical extractions and synchrotron-based X-ray absorption spectroscopy (XAS). Organic horizons across all polygon features (e.g., trough, ridge, and center) were enriched in extractable Fe and P relative to mineral horizons. Soil Fe was dominated by organic-bound Fe and short-range ordered Fe oxyhydroxides, while soil P was primarily associated with oxides and organic matter in organic horizons but apatite and/or calcareous minerals in mineral horizons. Iron oxyhydroxides and Fe-bound inorganic P (Pi) were most enriched at the soil surface and decreased gradually with depth, and Fe-bound Pi was >4× greater than water-soluble Pi. These results demonstrate that Fe-bound Pi is a large and ecologically important reservoir of phosphate. We contend that Fe oxyhydroxides and other minerals may regulate Pi solubility under fluctuating redox conditions in organic surface soils on the arctic tundra.
Original language | English |
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Pages (from-to) | 1475-1490 |
Number of pages | 16 |
Journal | Environmental Science: Processes and Impacts |
Volume | 22 |
Issue number | 7 |
DOIs | |
State | Published - Jul 2020 |
Funding
† This manuscript has been authored in part by UT-Battelle, LLC, under contract DE-AC05-00OR22725 with the US Department of Energy (DOE). The US government retains and the publisher, by accepting the article for publication, acknowledges that the US government retains a nonexclusive, paid-up, irrevocable, worldwide license to publish or reproduce the published form of this manuscript, or allow others to do so, for US government purposes. DOE will provide public access to these results of federally sponsored research in accordance with the DOE Public Access Plan (http://energy.gov/downloads/doe-public-access-plan). ‡ Electronic supplementary information (ESI) available. See DOI: 10.1039/d0em00142b This research was funded by National Science Foundation grant EAR-1609027 (Geobiology and Low-temperature Geochemistry) to Herndon and Kinsman-Costello. NGEE Arctic is funded through the Department of Energy (DOE) Office of Science, Biological and Environmental Research (BER) program (ERPK757). This research used resources of the Advanced Photon Source, a U.S. Department of Energy Office of Science user facility operated for DOE Office of Science by Argonne National Laboratory under contract DE-AC02-06CH11357. X-ray absorption spectra were collected at sector 12BM with support from Benjamin Reinhart.
Funders | Funder number |
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National Science Foundation | EAR-1609027 |
National Science Foundation | |
U.S. Department of Energy | |
Office of Science | |
Biological and Environmental Research | ERPK757 |
Biological and Environmental Research | |
Argonne National Laboratory | DE-AC02-06CH11357 |
Argonne National Laboratory |