20 research outputs found

    Distinct spatial dependency of carbon distribution between soil pools in grassland SOIL

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    Grassland soils play a key role in climate change and food security, and carbon (C) and nitrogen (N) mineralization is central to this. Although there are a number of mathematical models available to estimate C and N mineralization, they do not encompass the variability of the process and there is uncertainty in their predictions. The input parameters of the SOMA model (Soil Organic Matter “A”) have been conceptualized and validated to predict mineralization in arable soils. The objective of this research was to measure the spatial dependence of the input parameters in order to further ob - tain spatial predictions of mineralisation in a grassland system. A nested design was applied using sampling intervals of 30 m, 10 m, 1 m, and 0.12 m as sources of variation. From each sampling point a soil sample was taken (0-23 cm) and physical sequential fractionation was applied to obtain the free light fraction (FLF) and intra-aggregate light fraction (IALF). The C and N contents in the fractions were measured by mass spectrometry, and the results analysed by residual maximum likelihood (REML) to obtain components of variance at each stage, and then accumulated to plot the approach to a variogram. Both fractions showed spatial dependence at the finest scales measured, and the general pattern was different from that in an arable site. The recommended soil sampling interval where C and N mineralization predictions would be spatially distributed according to the correlation of input light fractions parameters of SOMA is 0.5m

    Passive CO<sub>2</sub> removal in urban soils:evidence from brownfield sites

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    Management of urban brownfield land can contribute to significant removal of atmospheric CO2 through the development of soil carbonate minerals. However, the potential magnitude and stability of this carbon sink is poorly quantified as previous studies address a limited range of conditions and short durations. Furthermore, the suitability of carbonate-sequestering soils for construction has not been investigated. To address these issues we measured total inorganic carbon, permeability and ground strength in the top 20 cm of soil at 20 brownfield sites in northern England, between 2015 and 2017. Across all sites accumulation occurred at a rate of 1–16 t C ha−1 yr−1, as calcite (CaCO3), corresponding to removal of approximately 4–59 t CO2 ha−1 yr−1, with the highest rate in the first 15 years after demolition. C and O stable isotope analysis of calcite confirms the atmospheric origin of the measured inorganic carbon. Statistical modelling found that pH and the content of fine materials (combined silt and clay content) were the best predictors of the total inorganic carbon content of the samples. Measurement of permeability shows that sites with carbonated soils possess a similar risk of run-off or flooding to sandy soils. Soil strength, measured as in-situ bearing capacity, increased with carbonation. These results demonstrate that the management of urban brownfield land to retain fine material derived from concrete crushing on site following demolition will promote calcite precipitation in soils, and so offers an additional CO2 removal mechanism, with no detrimental effect on drainage and possible improvements in strength. Given the large area of brownfield land that is available for development, the contribution of this process to CO2 removal by urban soils needs to be recognised in CO2 mitigation policies

    An empirical model approach for assessing soil organic carbon stock changes following biomass crop establishment in Britain

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    Land-use change (LUC) is a major influence on soil organic carbon (SOC) stocks and the global carbon cycle. LUC from conventional agricultural to biomass crops has increased in Britain but there is limited understanding of the effects on SOC stocks. Results from paired plot studies investigating site-specific effects document both increasing and decreasing SOC stocks over time. Such variation demonstrates the sensitivity of SOC to many factors including environmental conditions. Using a chronosequence of 93 biomass crop sites in England and Wales, mainly of 1–14 y age, empirical models were developed of SOC trajectory following LUC from arable and grassland to short rotation coppice (SRC) willow and Miscanthus production. SOC stocks were calculated for each site using a fixed sampling depth of 30 cm and changes were estimated by comparing with typical pre-conversion SOC stocks. Most LUCs had no demonstrable net effect on SOC stocks. An estimated net SOC loss of 45.2 ± 24.1 tonnes per hectare (±95% confidence intervals) occurred after 14 y following LUC from grassland to SRC willow. Soil texture and climate data for each site were included in multivariable models to assess the influence of different environmental conditions on SOC trajectory. In most cases the addition of explanatory variables improved the model fit. These models may provide some preliminary estimates of more region-specific changes in SOC following LUC. However, the model fit did not improve sufficiently as to provide a basis for adopting a more targeted LUC strategy for lignocellulosic biomass crop production

    Biochar and enhanced phosphate capture: Mapping mechanisms to functional properties

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    A multi-technique analysis was performed on a range of biochar materials derived from secondary organic resources and aimed at sustainable recovery and re-use of wastewater phosphorus (P). Our purpose was to identify mechanisms of P capture in biochar and thereby inform its future optimisation as a sustainable P fertiliser. The biochar feedstock comprised pellets of anaerobically digested sewage sludge (PAD) or pellets of the same blended in the ratio 9:1 with ochre sourced from minewater treatment (POCAD), components which have limited alternative economic value. In the present study the feedstocks were pyrolysed at two highest treatment temperatures of 450 and 550 °C. Each of the resulting biochars were repeatedly exposed to a 20 mg l−1 PO4-P solution, to produce a parallel set of P-exposed biochars. Biochar exterior and/or interior surfaces were quantitatively characterised using laser-ablation (LA)-ICP-MS, X-ray diffraction, X-ray photo-electron spectroscopy (XPS) and scanning electron microscopy coupled with energy dispersive X-ray. The results highlighted the general importance of Fe minerals in P capture. XPS analysis of POCAD550 indicated lower oxidation state Fe2p3 bonding compared to POCAD450, and LA-ICP-MS indicated stronger covariation of Fe and S, even after P exposure. This suggests that low-solubility Fe/S compounds are formed during pyrolysis, are affected by process parameters and impact on P capture. Other data suggested capture roles for aluminium, calcium and silicon. Overall, our analyses suggest that a range of mechanisms for P capture are concurrently active in biochar. We highlighted the potential to manipulate these through choice of form and composition of feedstock as well as pyrolysis processing, so that biochar may be increasingly tailored towards specific functionality

    Geotechnical requirements for capturing CO2 through highways land

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    Roadside verges in Britain support 238,000 hectares of vegetated land and approximately 10 hectares of vegetated central reserves. These areas have the potential to be engineered in such a way that they deliver a range of ecosystem services including flood regulation and biodiversity conservation in addition to their primary functions such as comfort of sidewalk users (mostly un-vegetated), protection of spray from passing vehicles, a space for benches, bus shelters, street lights and other public amenities, and visual improvement of the roads and designated green belts. Previous research has shown that in soils, calcium-rich materials such as recycled crushed concrete or natural crushed dolerite undergo carbonation. This effectively captures CO2 from the atmosphere and stores it in the form of CaCO3 precipitated between soil particles. Engineering this process can potentially assist the UK in achieving its ambitious target to reduce CO2 emissions by 80% of 1990 levels by 2050. Rates of carbonation measured at urban brownfield sites in the UK suggest that treating 12,000 hectares of land containing suitable amendments could remove 1 million tonne CO2 annually. However, brownfield sites are often subjected to re-construction activities which would reduce the rate of CO2 absorption from the atmosphere by sealing. To optimize the rate of carbonation, engineered soils need to be constructed at locations subjected to least post-construction activities and roadside verges and central reserves represent a key opportunity in this regard. This paper calculates limits to CaCO3 formation within the first 1 m of pore spaces of soils at roadside verges and central reserves in Britain considering a soil porosity of 20%

    Trends in the recovery of phosphorus in bioavailable forms from wastewater

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    Addressing food security issues arising from phosphorus (P) scarcity is described as one of the greatest global challenges of the 21st Century. Dependence on inorganic phosphate fertilisers derived from limited geological sources of P creates an urgent need to recover P from wastes and treated waters, in safe forms that are also effective agriculturally – the established process of P removal by chemical precipitation using Fe or Al salts, is effective for P removal but leads to residues with limited bioavailability and contamination concerns. One of the greatest opportunities for P recovery is at wastewater treatment plants (WWTPs) where the crystallisation of struvite and Ca-P from enhanced biological P removal (EBPR) sludge is well developed and already shown to be economically and operationally feasible in some WWTPs. However, recovery through this approach can be limited to &lt;25% efficiency unless chemical extraction is applied. Thermochemical treatment of sludge ash produces detoxified residues that are currently utilised by the fertiliser industry; wet chemical extraction can be economically feasible in recovering P and other by-products. The bioavailability of recovered P depends on soil pH as well as the P-rich material in question. Struvite is a superior recovered P product in terms of plant availability, while use of Ca-P and thermochemically treated sewage sludge ash is limited to acidic soils. These technologies, in addition to others less developed, will be commercially pushed forward by revised fertiliser legislation and foreseeable legislative limits for WWTPs to achieve discharges of &lt;1 mg P/L

    The priming potential of environmentally weathered pyrogenic carbon during land-use transition to biomass crop production

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    Since land-use change (LUC) to lignocellulosic biomass crops often causes a loss of soil organic carbon (SOC), at least in the short term, this study investigated the potential for pyrogenic carbon (PyC) to ameliorate this effect. Although negative priming has been observed in many studies, most of these are long-term incubation experiments which do not account for the interactions between environmentally weathered PyC and native SOC. Here, the aim was to assess the impact of environmentally weathered PyC on native SOC mineralization at different time points in LUC from arable crops to short rotation coppice (SRC) willow. At eight SRC willow plantations in England, with ages of 3–22 years, soil amended 18–22 months previously with PyC was compared with unamended control soil. Cumulative CO2 flux was measured weekly from incubated soil at 0–5 cm depth, and soil-surface CO2 flux was also measured in the field. For the incubated soil, cumulative CO2 flux was significantly higher from soil containing weathered PyC than the control soil for seven of the eight sites. Across all sites, the mean cumulative CO2 flux was 21% higher from soil incubated with weathered PyC than the control soil. These results indicate the potential for positive priming in the surface 5 cm of soil independent of changes in soil properties following LUC to SRC willow production. However, no net effect on CO2 flux was observed in the field, suggesting this increase in CO2 is offset by a contrasting PyC-induced effect at a different soil depth or that different effects were observed under laboratory and field conditions. Although the mechanisms for these contrasting effects remain unclear, results presented here suggest that PyC does not reduce LUC-induced SOC losses through negative priming, at least for this PyC type and application rate
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