Land-use changes are the second largest source of human-induced greenhouse gas emission, mainly due to deforestation in the tropics and subtropics. CO 2 emissions result from biomass and soil organic carbon (SOC) losses and may be offset with afforestation programs. However, the effect of land-use changes on SOC is poorly quantified due to insufficient data quality (only SOC concentrations and no SOC stocks, shallow sampling depth) and representativeness. In a global meta-analysis, 385 studies on land-use change in the tropics were explored to estimate the SOC stock changes for all major land-use change types. The highest SOC losses were caused by conversion of primary forest into cropland (À25%) and perennial crops (À30%) but forest conversion into grassland also reduced SOC stocks by 12%. Secondary forests stored less SOC than primary forests (À9%) underlining the importance of primary forests for C stores. SOC losses are partly reversible if agricultural land is afforested (1 29%) or under cropland fallow (1 32%) and with cropland conversion into grassland (1 26%). Data on soil bulk density are critical in order to estimate SOC stock changes because (i) the bulk density changes with land-use and needs to be accounted for when calculating SOC stocks and (ii) soil sample mass has to be corrected for bulk density changes in order to compare land-use types on the same basis of soil mass. Without soil mass correction, land-use change effects would have been underestimated by 28%. Land-use change impact on SOC was not restricted to the surface soil, but relative changes were equally high in the subsoil, stressing the importance of sufficiently deep sampling.
Land-use change (LUC) is a major driving factor for the balance of soil organic carbon (SOC) stocks and the global carbon cycle. The temporal dynamic of SOC after LUC is especially important in temperate systems with a long reaction time. On the basis of 95 compiled studies covering 322 sites in the temperate zone, carbon response functions (CRFs) were derived to model the temporal dynamic of SOC after five different LUC types (mean soil depth of 30 AE 6 cm). Grassland establishment caused a long lasting carbon sink with a relative stock change of 128 AE 23% and afforestation on former cropland a sink of 116 AE 54%, 100 years after LUC (mean AE 95% confidence interval). No new equilibrium was reached within 120 years. In contrast, there was no SOC sink following afforestation of grasslands and 75% of all observations showed SOC losses, even after 100 years. Only in the forest floor, there was carbon accumulation of 0.38 AE 0.04 Mg ha À1 yr À1 in afforestations adding up to 38 AE 4 Mg ha À1 labile carbon after 100 years. Carbon loss after deforestation (À32 AE 20%) and grassland conversion to cropland (À36 AE 5%), was rapid with a new SOC equilibrium being reached after 23 and 17 years, respectively. The change rate of SOC increased with temperature and precipitation but decreased with soil depth and clay content. Subsoil SOC changes followed the trend of the topsoil SOC changes but were smaller (25 AE 5% of the total SOC changes) and with a high uncertainty due to a limited number of datasets. As a simple and robust model approach, the developed CRFs provide an easily applicable tool to estimate SOC stock changes after LUC to improve greenhouse gas reporting in the framework of UNFCCC.
Bioenergy from crops is expected to make a considerable contribution to climate change mitigation. However, bioenergy is not necessarily carbon neutral because emissions of CO 2 , N 2 O and CH 4 during crop production may reduce or completely counterbalance CO 2 savings of the substituted fossil fuels. These greenhouse gases (GHGs) need to be included into the carbon footprint calculation of different bioenergy crops under a range of soil conditions and management practices. This review compiles existing knowledge on agronomic and environmental constraints and GHG balances of the major European bioenergy crops, although it focuses on dedicated perennial crops such as Miscanthus and short rotation coppice species. Such second-generation crops account for only 3% of the current European bioenergy production, but field data suggest they emit 40% to >99% less N 2 O than conventional annual crops. This is a result of lower fertilizer requirements as well as a higher N-use efficiency, due to effective N-recycling. Perennial energy crops have the potential to sequester additional carbon in soil biomass if established on former cropland (0.44 Mg soil C ha À1 yr À1 for poplar and willow and 0.66 Mg soil C ha À1 yr À1 for Miscanthus). However, there was no positive or even negative effects on the C balance if energy crops are established on former grassland. Increased bioenergy production may also result in direct and indirect land-use changes with potential high C losses when native vegetation is converted to annual crops. Although dedicated perennial energy crops have a high potential to improve the GHG balance of bioenergy production, several agronomic and economic constraints still have to be overcome.Keywords: biofuel, carbon debt, carbon footprint, land management, methane, Miscanthus, nitrous oxide, short rotation coppice, soil organic carbon Greenhouse gas saving with bioenergy -a European perspectiveThe European Union has committed to increase the proportion of renewable energy from 9% in 2010 to 20% of Correspondence: Axel Don,
Abstract. Soil moisture is of primary importance for predicting the evolution of soil carbon stocks and fluxes, both because it strongly controls organic matter decomposition and because it is predicted to change at global scales in the following decades. However, the soil functions used to model the heterotrophic respiration response to moisture have limited empirical support and introduce an uncertainty of at least 4% in global soil carbon stock predictions by 2100. The necessity of improving the representation of this relationship in models has been highlighted in recent studies. Here we present a data-driven analysis of soil moisture-respiration relations based on 90 soils. With the use of linear models we show how the relationship between soil heterotrophic respiration and different measures of soil moisture is consistently affected by soil properties. The empirical models derived include main effects and moisture interaction effects of soil texture, organic carbon content and bulk density. When compared to other functions currently used in different soil biogeochemical models, we observe that our results can correct biases and reconcile differences within and between such functions. Ultimately, accurate predictions of the response of soil carbon to future climate scenarios will require the integration of soil-dependent moisture-respiration functions coupled with realistic representations of soil water dynamics.
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