Dissolved organic carbon (DOC) plays an important role in global and regional carbon cycles. However, the quantification of DOC in forest ecosystems remains uncertain. Here, the processed-based biogeochemical model TRIPLEX-DOC was modified by optimizing the function of soil organic carbon distribution with increasing depths, as well as DOC sorption-desorption efficiency. The model was validated by field measurements of DOC concentration and flux at five forest sites and Beijiang River basin in monsoon regions of China. Model validation indicated that seasonal patterns of DOC concentration across climatic zones were different, and these differences were captured by our model. Importantly, the modified model performed better than the original model. Indeed, model efficiency of the modified model increased from -0.78 to 0.19 for O horizon predictions, and from -0.46 to 0.42 for the mineral soils predictions. Likewise, DOC fluxes were better simulated by the modified model. At the site scale, the simulated DOC fluxes were strongly correlated with the observed values (R = 0.97, EF = 0.91). At the regional scale, the DOC flux predicted in the Beijiang River basin was 16.44 kg C/ha, which was close to the observed value of 17 kg C/ha. Using sensitivity analysis, we showed that temperature, precipitation and temperature sensitivity of DOC decomposition (Q) were the most sensitive parameters when predicting DOC concentrations and fluxes in forest soils. We also found that both the percentage of DOC flux to forest net ecosystem productivity, and the retention of DOC by mineral soil were highly correlated with the amount of precipitation. Overall, our model validations indicated that the modified TRIPLEX-DOC model is a useful tool for simulating the dynamics of DOC concentrations and fluxes in forest ecosystems. We highlight that more accurate estimates of parameter Q in deep mineral soils can reduce model uncertainty, when simulating DOC concentrations and fluxes in forest soils.
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http://dx.doi.org/10.1016/j.scitotenv.2019.134054 | DOI Listing |
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