A dual isotope approach to isolate soil carbon pools of different turnover times
- 1Earth Sciences Division, Lawrence Berkeley National Laboratory, Berkeley CA 94720, USA
- 2Energy and Resources Group, University of California, Berkeley, CA 94720, USA
- 3Department of Crop and Soil Science, Oregon State University, Corvallis, OR 97331, USA
- 4Department of Environmental Studies, University of California, Santa Cruz, CA 95064, USA
- 5Department of Global Ecology, Carnegie Institution for Science, Stanford, CA 94305, USA
- 6Department of Biogeochemical Processes, Max Planck Institute for Biogeochemistry, 07745 Jena, Germany
Abstract. Soils are globally significant sources and sinks of atmospheric CO2. Increasing the resolution of soil carbon turnover estimates is important for predicting the response of soil carbon cycling to environmental change. We show that soil carbon turnover times can be more finely resolved using a dual isotope label like the one provided by elevated CO2 experiments that use fossil CO2. We modeled each soil physical fraction as two pools with different turnover times using the atmospheric 14C bomb spike in combination with the label in 14C and 13C provided by an elevated CO2 experiment in a California annual grassland. In sandstone and serpentine soils, the light fraction carbon was 21–54% fast cycling with 2–9 yr turnover, and 36–79% slow cycling with turnover slower than 100 yr. This validates model treatment of the light fraction as active and intermediate cycling carbon. The dense, mineral-associated fraction also had a very dynamic component, consisting of ∼7% fast-cycling carbon and ∼93% very slow cycling carbon. Similarly, half the microbial biomass carbon in the sandstone soil was more than 5 yr old, and 40% of the carbon respired by microbes had been fixed more than 5 yr ago. Resolving each density fraction into two pools revealed that only a small component of total soil carbon is responsible for most CO2 efflux from these soils. In the sandstone soil, 11% of soil carbon contributes more than 90% of the annual CO2 efflux. The fact that soil physical fractions, designed to isolate organic material of roughly homogeneous physico-chemical state, contain material of dramatically different turnover times is consistent with recent observations of rapid isotope incorporation into seemingly stable fractions and with emerging evidence for hot spots or micro-site variation of decomposition within the soil matrix. Predictions of soil carbon storage using a turnover time estimated with the assumption of a single pool per density fraction would greatly overestimate the near-term response to changes in productivity or decomposition rates. Therefore, these results suggest a slower initial change in soil carbon storage due to environmental change than has been assumed by simpler (one-pool) mass balance calculations.