Journal
BIOGEOSCIENCES
Volume 13, Issue 16, Pages 4777-4788Publisher
COPERNICUS GESELLSCHAFT MBH
DOI: 10.5194/bg-13-4777-2016
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Funding
- DOE [DE-SC0014275]
- University of Nevada-Reno Start-up Fund
- CFI
- NSERC
- University of Saskatchewan
- Government of Saskatchewan
- WED Canada
- NRC Canada
- CIHR
- EPA Science-To-Achieve-Results (STAR) grant [R833378]
- EPA [909229, R833378] Funding Source: Federal RePORTER
- U.S. Department of Energy (DOE) [DE-SC0014275] Funding Source: U.S. Department of Energy (DOE)
- Directorate For Geosciences
- Office of Polar Programs (OPP) [1739567] Funding Source: National Science Foundation
- Division Of Environmental Biology
- Direct For Biological Sciences [1027341] Funding Source: National Science Foundation
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Iron oxide minerals play an important role in stabilizing organic carbon (OC) and regulating the biogeochemical cycles of OC on the earth surface. To predict the fate of OC, it is essential to understand the amount, spatial variability, and characteristics of Fe-bound OC in natural soils. In this study, we investigated the concentrations and characteristics of Fe-bound OC in soils collected from 14 forests in the United States and determined the impact of ecogeographical variables and soil physicochemical properties on the association of OC and Fe minerals. On average, Fe-bound OC contributed 37.8% of total OC (TOC) in forest soils. Atomic ratios of OC: Fe ranged from 0.56 to 17.7, with values of 1-10 for most samples, and the ratios indicate the importance of both sorptive and incorporative interactions. The fraction of Fe-bound OC in TOC (f(Fe-OC)) was not related to the concentration of reactive Fe, which suggests that the importance of association with Fe in OC accumulation was not governed by the concentration of reactive Fe. Concentrations of Fe-bound OC and f(Fe-OC) increased with latitude and reached peak values at a site with a mean annual temperature of 6.6 degrees C. Attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR) and near-edge X-ray absorption fine structure (NEXAFS) analyses revealed that Fe-bound OC was less aliphatic than non-Fe-bound OC. Fe-bound OC also was more enriched in C-13 compared to the non-Fe-bound OC, but C/N ratios did not differ substantially. In summary, C-13-enriched OC with less aliphatic carbon and more carboxylic carbon was associated with Fe minerals in the soils, with values of f(Fe-OC) being controlled by both sorptive and incorporative associations between Fe and OC. Overall, this study demonstrates that Fe oxides play an important role in regulating the biogeochemical cycles of C in forest soils and uncovers the governing factors for the spatial variability and characteristics of Fe-bound OC.
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