Environmental and human influences on organic carbon fractions down the soil profile
Introduction
Soil organic carbon (SOC) represents a large component of the global carbon cycle, with around 1500 Pg of organic carbon stored in the top meter of soil (Jobbagy and Jackson, 2000), and between 2344 (Jobbagy and Jackson, 2000) and 2400 Pg (Batjes, 1996) stored in the top 2–3 m of soils worldwide. Due to its origins in plant photosynthesis and loss via heterogenic respiration (predominately via soil microbial activity) it is a highly dynamic part of the global carbon cycle (Batjes, 1996).
Conceptually, SOC is separated into numerous pools with varying turnover rates ranging from hours to millennia (Trumbore, 1997), which are linked with the bioavailability of SOC and therefore its degradability (Baldock and Skjemstad, 2000). Mechanisms such as mineral-association (Oades, 1988), aggregation (and associated occlusion of SOC in aggregate interiors) (Tisdall and Oades, 1982) and physico-chemical transformation (e.g. via pyrolysis, Skjemstad et al., 1996) can reduce the biological accessibility of organic matter, converting it into more stable forms which are resistant to degradation processes and remain in the soil environment for long time periods.
Such pools of organic matter have been successfully isolated using physico-chemical fractionation procedures (e.g. Christensen, 1992, Golchin et al., 1994) which can be used to initialize soil carbon turnover models (Skjemstad et al., 2004), providing a link between measurable SOC fractions and conceptualized SOC pools. Recent advancements have provided the ability to detect different carbon pools without physico-chemical fractionation of soil samples, instead relying on mid-infrared (MIR) spectra. Baldock et al. (2013a) applied partial least square regression (PLSR) analyses to MIR spectra to derive predictive algorithms to estimate three SOC fractions of conceptually differing bioavailability. Particulate organic carbon (POC) was linked with fresh, more easily decomposable organic material; humus organic carbon (HOC) represented a fraction of SOC which has been altered from its initial state via decomposition, mineral-association and aggregation processes. Resistant organic carbon (ROC) represented a biologically resistant poly-aryl carbon fraction with long residence time in soils (Baldock et al., 2013b).
These three SOC fractions are therefore conceptually associated with different processes and mechanisms driving SOC dynamics, namely production (POC, via photosynthesis, although turnover will reduce POC), turnover and retention (HOC, via microbiological activity and diagenesis with subsequent sorption on mineral surfaces and/or occlusion in aggregates) and abiotic transformation (ROC, i.e. alteration in fire). Thus POC represents a more labile pool of SOC, whereas HOC and ROC represent SOC pools of greater stability which will remain in soils for longer time periods. Identifying what drives not only the total amount of SOC in soils, but also the relative proportions of these fractions is fundamental to our understanding of SOC dynamics and the processes controlling it. This understanding will not only enable us to manage our soil carbon reserves for the future, but also to interpret SOC response to past environmental changes.
Recent work investigating the factors affecting the stock of these three fractions (POC, HOC, ROC) in eastern Australian soils showed that environmental and site properties exert the greatest influence, with human activities contributing a lesser, but still substantial amount to the variance in the fractions (Rabbi et al., 2014). This is consistent with investigations into the drivers of total SOC storage in eastern Australia, which have been identified as climate, soil texture and bulk density related, with the effects of land-use on SOC being negligible at the surface (Rabbi et al., 2015) but becoming more important with increasing soil depth (Hobley et al., 2015).
However, like many studies into SOC dynamics in Australia, these investigations focused on processes within the top 30 cm of soil. Subsoil organic carbon comprises a large (∼70% of SOC is located below the top 20 cm, Jobbagy and Jackson, 2000) yet still poorly understood (Rumpel and Kögel-Knabner, 2011) component of the global carbon cycle. With increasing depth from the surface, soil organic matter generally increases in age (e.g. Hobley et al., 2013, Kaiser et al., 2002), implying enhanced stability, and its utilization as a carbon source by microorganisms is altered (Kramer and Gleixner, 2008) implying different carbon dynamics at depth than at the surface. Understanding soil organic carbon dynamics and its role in the global carbon cycle therefore requires investigation of both topsoils and subsoils.
In this study we investigated controls on SOC dynamics and stability down the soil profile to depths of up to 1 m. Several hypotheses were tested relating to the drivers of the SOC fractions:
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That the relative contribution of POC would be driven by similar factors to the drivers of surface SOC, predominately climate variables related to water availability (Hobley et al., 2015), as this fraction is related to plant productivity. Land-use will negatively affect the relative contribution of POC to SOC via lowered input in agricultural systems (most notably in cropped systems) compared with native vegetation systems (Hobley et al., 2015, Hobley and Wilson, 2016, Rabbi et al., 2014);
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In contrast, we hypothesized that the relative contribution of HOC to SOC will be driven more by soil physico-chemical properties such as texture and pH, as this fraction is associated with SOC turnover and retention on soil minerals, which are influenced by the soil physico-chemical environment. As a driver of SOC turnover, temperature will also be important to this fraction.
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ROC will likely be affected by both climate and anthropogenic factors, as temperature, vegetation type and human fire management will dictate the (unknown) fire histories of the sites.
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Lastly, we hypothesized that, associated with the generally greater age (and by implication stability) of subsoil OC than surface OC, the relative contribution of the labile POC fraction will decrease with depth whereas relative contributions of the more stable ROC and HOC fractions will increase with depth.
To test these hypotheses we quantified the concentrations of SOC fractions as predicted from MIR spectra acquired from different soil depths of 100 soil profiles sampled at 100 sites from across New South Wales, eastern Australia and used several data-mining approaches to model and investigate the factors accounting for variations in SOC composition.
Section snippets
Soils and sites
The State of New South Wales covers a large region of over 800,000 km2 in eastern Australia. Although largely within the global temperate zone, temperatures range from winter minima of <0 °C to summer maxima>45 °C depending on altitude and proximity to the coast. Mean annual precipitation (MAP) varies considerably, ranging from <200 mm yr−1 in the west to>1500 mm yr‐1 in the North–East (Australian Government Bureau of Meteorology, 2012). For this study, 100 sites across New South Wales (Fig. 1) were
MIR predictions
SOC contents predicted using BSL, SG and AVE techniques were generally well correlated (R = 0.94 for BSL, 0.92 for SG, 0.95 for AVE estimates) to SOC contents measured using a dry combustion technique (Hobley and Wilson, 2016) up to ∼8% but were poor at higher concentrations (Fig. 2). Although this does not necessarily indicate a failure of the predictions of the individual fractions at SOC contents above this value, the reliability of such estimates cannot be assessed without further analyses
Model performance and interpretation
Although the individual data-mining models identified (at times) different variables of differing importance, all models were informative and their results lead to similar conclusions. The generally good to very good explanation of variance (c.f. Balshi et al., 2009, Hobley et al., 2015, Wiesmeier et al., 2014), indicates the suitability of these modelling approaches for investigating SOC dynamics and fractions. Using a consensus approach based upon multiple models can help to eliminate bias of
Conclusions
The modern statistical techniques employed here enabled us to investigate the relative allocation of SOC to three of its component fractions – particulate, humus and resistant organic carbon – down the entire soil profile without the requirements of data normality and homoscedasticity which can limit traditional statistical applications, enabling us to simultaneously examine the allocation of SOC to fractions across numerous, at times inconsistent, sampling depths and over a wide range of SOC
Acknowledgements
This research was supported by funding from the Australian Government Department of Agriculture. Thank you to Bruce Hawke, Kristen Clancy and Mano Veeragathipillai for laboratory work and to Arjan Wilkie for the map.
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