Potential Contribution of Combined Atmospheric Ca2+ and Mg2+ Wet Deposition Within the Continental U.S. to Soil Inorganic Carbon Sequestration

Abstract

Abstract Soil inorganic carbon (SIC) stocks continuously change from the formation of pedogenic carbonates, a process requiring inputs of Ca 2+ and Mg 2+ ions. This study ranked the soil orders in terms of potential inorganic carbon sequestration resulting from wet Ca 2+ and Mg 2+ deposition from 1994 to 2003 within the continental United States. The analysis revealed that average annual atmospheric wet deposition of Ca 2+ and Mg 2+ was the highest in the Central Midwest-Great Plains region, likely due to soil particle input from loess-derived soils. The soil orders receiving the highest total average annual atmospheric wet Ca 2+ and Mg 2+ deposition, expressed as potential inorganic carbon formation (barring losses from erosion and leaching), were: 1) Mollisols (1.1 × 10 8 kg C), 2) Alfisols (8.4 × 10 7 kg C), 3) Entisols (3.8 × 10 7 kg C), and 4) Aridisols (2.8 × 10 7 kg C). In terms of area-normalized result, the soil orders were ranked: 1) Histosols (73 kg C km −2 ), 2) Alfisols and Vertisols (64 kg C km −2 ), 3) Mollisols (62 kg C km −2 ), and 4) Spodosols (52 kg C km −2 ). The results of this study provide an estimate of potential soil inorganic carbon sequestration as a result of atmospheric wet Ca 2+ and Mg 2+ deposition, and this information may be useful in assessing dynamic nature of soil inorganic carbon pools.