方解石
碳酸盐
钙质的
土壤水分
土壤碳
矿物学
碳纤维
化学
环境化学
分析化学(期刊)
地质学
材料科学
土壤科学
有机化学
复合材料
古生物学
复合数
作者
Joséphine Hazera,Isabelle Kowalewski,David Sebag,Eric Verrecchia,Herman Ravelojaona,Tiphaine Chevallier
摘要
ABSTRACT Studying the soil organic and inorganic carbon (SOC and SIC) dynamics is essential to assess the carbon (C) sequestration potential of calcareous soils. Isotopic signatures (δ 13 C) are used to assess the C origin of SOC or SIC. However, as measuring SOC and SIC contents, measuring δ 13 C SOC and δ 13 C SIC on a non‐pretreated aliquot remains a challenge. Thermal analyses, like the Rock‐Eval (RE) analysis, are promising to quantify SOC and SIC in a single analysis, but, to our knowledge, no development was conducted to assess δ 13 C SOC and δ 13 C SIC . We coupled a RE device to an isotopic gas analyser (Picarro) to continuously measure δ 13 C CO2 and approach δ 13 C SOC and δ 13 C SIC . We hypothesised that different carbonate mineralogies and/or crystal sizes in SIC involve fluctuations of the δ 13 C CO2 . Two calcareous soils, a lithogenic (calcite) and a biogenic (snail shell) carbonate, and five calcite/shell mixes were analysed with the RE‐Picarro setup. Two distinct δ 13 C CO2 values were obtained before and after 650°C and were consistent with the δ 13 C SOC and δ 13 C SIC obtained by EA‐IRMS. The fluctuations of δ 13 C CO2 above 650°C were higher with calcite/shell mixes than with pure carbonates. A δ 13 C CO2 fluctuation > ± 0.2‰ could be a pertinent indicator to detect mixes of carbonate with different δ 13 C in soils. The RE‐Picarro setup is promising to assess SOC and SIC contents, δ 13 C SOC and δ 13 C SIC and detect mixes of carbonate with different origin on a non‐pretreated aliquot. Development is needed (i) on more soil and carbonate samples and (ii) to improve the precision and accuracy of the RE‐Picarro setup.
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