X 射线化学成像技术用于评估土壤和沉积物中的氧化还原微位点

Vincent Noël, K. Boye, Hannah R. Naughton, E. Lacroix, Meret Aeppli, Naresh Kumar, S. Fendorf, Samuel M. Webb
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引用次数: 0

摘要

氧化还原反应是多种生物地球化学过程的基础,在土壤和沉积物中通常具有时空异质性。然而,氧化还原异质性尚未被纳入土壤生物地球化学的主流概念和建模中。缺氧微地是土壤氧化还原异质性的一个显著特点,它是在其他含氧环境中的非主要耗氧区。忽略缺氧微地可能会给温室气体排放、碳螯合以及生态系统到全球范围内的养分和污染物循环的定量评估带来重大不确定性。然而,只有少数研究对未扰动土壤中的缺氧微地进行了观测/表征,这主要是因为土壤是不透明的,而且微地需要微米-厘米尺度的分辨率,而不是厘米-米尺度的分辨率。因此,我们目前对微生境特征的了解并不支持模型参数化。为了解决这一知识空白,我们通过这项概念验证研究证明,X 射线荧光 (XRF) 二维绘图可以利用固相 "法医 "证据可靠地检测、量化缺氧微地,并提供基本的氧化还原特征。首先,我们测试并开发了一种系统的数据处理方法,以消除在人工注入微点的 "富 "铁沉积岩芯中,通过同步辐射多能 XRF 二维绘图检测到的氧化还原微点假阳性(即伪影)。然后,以 1-100 µm 的分辨率绘制了完整的天然土壤岩芯切片(长度/宽度超过 cm-m)中 FeII 和 FeIII 物种的空间分布图。这些研究揭示了在主要含氧土壤(如橡树稀树草原和山区流域的山坡土壤)中存在缺氧微地的直接证据,而在这些土壤中通常不会出现厌氧现象。我们还揭示了氧化还原微位点在橡树稀树草原土壤聚集体中的优先空间分布。我们预计,这种方法将促进我们对土壤生物地球化学的了解,并有助于解决名义上含氧土壤中还原产物的 "异常 "现象。
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X-ray chemical imaging for assessing redox microsites within soils and sediments
Redox reactions underlie several biogeochemical processes and are typically spatiotemporally heterogeneous in soils and sediments. However, redox heterogeneity has yet to be incorporated into mainstream conceptualizations and modeling of soil biogeochemistry. Anoxic microsites, a defining feature of soil redox heterogeneity, are non-majority oxygen depleted zones in otherwise oxic environments. Neglecting to account for anoxic microsites can generate major uncertainties in quantitative assessments of greenhouse gas emissions, C sequestration, as well as nutrient and contaminant cycling at the ecosystem to global scales. However, only a few studies have observed/characterized anoxic microsites in undisturbed soils, primarily, because soil is opaque and microsites require µm-cm scale resolution over cm-m scales. Consequently, our current understanding of microsite characteristics does not support model parameterization. To resolve this knowledge gap, we demonstrate through this proof-of-concept study that X-ray fluorescence (XRF) 2D mapping can reliably detect, quantify, and provide basic redox characterization of anoxic microsites using solid phase “forensic” evidence. First, we tested and developed a systematic data processing approach to eliminate false positive redox microsites, i.e., artefacts, detected from synchrotron-based multiple-energy XRF 2D mapping of Fe (as a proxy of redox-sensitive elements) in Fe-“rich” sediment cores with artificially injected microsites. Then, spatial distribution of FeII and FeIII species from full, natural soil core slices (over cm-m lengths/widths) were mapped at 1–100 µm resolution. These investigations revealed direct evidence of anoxic microsites in predominantly oxic soils such as from an oak savanna and toeslope soil of a mountainous watershed, where anaerobicity would typically not be expected. We also revealed preferential spatial distribution of redox microsites inside aggregates from oak savanna soils. We anticipate that this approach will advance our understanding of soil biogeochemistry and help resolve “anomalous” occurrences of reduced products in nominally oxic soils.
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