Mechanisms to mitigate global climate change by sequestering carbon (C) in different 'sinks' have been proposed as at least temporary measures. Of the major global C pools, terrestrial ecosystems hold the potential to capture and store substantially increased volumes of C in soil organic matter (SOM) through changes in management that are also of benefit to the multitude of ecosystem services that soils provide. This potential can only be realized by determining the amount of SOM stored in soils now, with subsequent quantification of how this is affected by management strategies intended to increase SOM concentrations, and used in soil C models for the prediction of the roles of soils in future climate change. An apparently obvious method to increase C stocks in soils is to augment the soil C pools with the longest mean residence times (MRT). Computer simulation models of soil C dynamics, e.g. RothC and Century, partition these refractory constituents into slow and passive pools with MRTs of centuries to millennia. This partitioning is assumed to reflect: (i) the average biomolecular properties of SOM in the pools with reference to their source in plant litter, (ii) the accessibility of the SOM to decomposer organisms or catalytic enzymes, or (iii) constraints imposed on decomposition by environmental conditions, including soil moisture and temperature. However, contemporary analytical approaches suggest that the chemical composition of these pools is not necessarily predictable because, despite considerable progress with understanding decomposition processes and the role of decomposer organisms, along with refinements in simulation models, little progress has been made in reconciling biochemical properties with the kinetically defined pools. In this review, we will explore how advances in quantitative analytical techniques have redefined the new understanding of SOM dynamics and how this is affecting the development and application of new modelling approaches to soil C.

Soil organic carbon (SOC) changes associated with land conversion to energy crops are central to the debate on bioenergy and their potential carbon neutrality. Here, the experimental evidence on SOC under perennial energy crops (PECs) is synthesised to parameterise a whole systems model and to identify uncertainties and knowledge gaps determining PECs being a sink or source of greenhouse gas (GHG). For Miscanthus and willow (Salix spp.) and their analogues (switchgrass, poplar), we examine carbon (C) allocation to above- and belowground residue inputs, turnover rates and retention in the soil. A meta-analysis showed that studies on dry matter partitioning and C inputs to soils are plentiful, whilst data on turnover are rare and rely on few isotopic C tracer studies. Comprehensive studies on SOC dynamics and GHG emissions under PECs are limited and subsoil processes and C losses through leaching remain unknown. Data showed dynamic changes of gross C inputs and SOC stocks depending on stand age. C inputs and turnover can now be specifically parameterised in whole PEC system models, whilst dependencies on soil texture, moisture and temperature remain empirical. In conclusion, the annual net SOC storage change exceeds the minimum mitigation requirement (0.25 Mg C ha−1 year−1) under herbaceous and woody perennials by far (1.14 to 1.88 and 0.63 to 0.72 Mg C ha−1 year−1, respectively). However, long-term time series of field data are needed to verify sustainable SOC enrichment, as the physical and chemical stabilities of SOC pools remain uncertain, although they are essential in defining the sustainability of C sequestration (half-life >25 years).

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The ability of soil to resist and recover from anthropogenic and environmental stresses defines stability and resilience, respectively; an understanding of this ability is critical to sustainable land-use. In this study of 26 soils from across Scotland, we examine the influence of soil properties and antecedent conditions on physical and biological resilience to stress. The sites studied covered a wide range of soil types and land management, including serpentine soil from the Shetland Islands, a catena on the Highland Boundary Fault, and young aeolian sandy soils on the east coast. Biological resilience was measured as CO 2 evolution from soil with added plant residues after either a transient (heat) or a persistent (copper) stress. Measures of physical resilience were: (i) compression and expansion indices following rapid uniaxial compression (to 50 kPa) and relaxation; and (ii) void ratio changes due to an overburden stress and subsequent cycles of wetting and drying. Evolution of CO 2 from soil with added plant residues after heat or copper stress ranged from 23% to >100% that of the unperturbed soil, while the air-filled void ratio after the overburden stress ranged from 70% to >100% that of the unperturbed soil. Soils were grouped into quartiles based on their resistance to and recovery after each of the four prescribed stresses. Soil organic carbon (SOC) content correlated strongly with resilience after biological and physical stresses, particularly resistance to Cu stress (r ¼ 0.72) and recovery from compression (r ¼ 0.67), whereas there were no strong correlations between resilience following heat and any of the measured soil characteristics, although both land use and soil class were helpful in separating the responses. Resistance to compression was negatively correlated with SOC (r ¼ -0.63).