Non-silicate iron in mineral-associated organic matter of agro-chernozems located on different positions on the slope

Q4 Agricultural and Biological Sciences Biulleten'' Pochvennogo instituta im VV Dokuchaeva Pub Date : 2023-08-04 DOI:10.19047/0136-1694-2023-115-54-86
E. V. Tsomaeva, Z. Artemyeva, E. Zasukhina, E. Varlamov
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Abstract

Data on total non-silicate iron (Fed) content in mineral-associated organic matter (MAOM) of agro-chernozems of different localization on the slope are presented. The distribution of total non-silicate iron in soil profile follows that of organic carbon (OC): the maximum values are confined to the surface horizons, and decrease down the profile. It has been revealed that the change in the content of non-silicate iron in the MAOM of the clay fraction in arable horizons of eroded agro-chernozems is a result of erosion processes, including their intensity, which also depends, among other things, on the slope steepness. A lower slope steepness (4°) contributes to an increase in the organic carbon loading on iron oxides, resulting in an increased in iron desorption capacity, while a higher slope steepness (6°) results in lower iron desorption capacity. The OC/Fed molar ratio is suggested as an additional indicator of the degree of soil erosion. In clay fractions, of both their position in the soil profile and their position on the slope, the predominant mechanism of organic matter stabilization was the formation of organic-iron complexes (OC/Fed > 10). In the Residue fraction of humus horizons, non-silicate iron seems to be presented mainly as iron carbonates (FeCO3), while the proportion of microaggregates (stable under the sonication), where OM is mainly humin, is relatively low against the background of the absolute dominance of primary minerals in this fraction (weight %). Most of the non-silicate iron of mineralassociated OM extracted by dithionite-citrate-hydrocarbonate is localized in the clay fraction – 2/3 or more.
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坡面不同位置农用黑钙土矿物伴生有机质中的非硅酸铁
介绍了坡面上不同定位的农用黑钙土矿物有机质中非硅酸铁(Fed)总含量的数据。土壤剖面中总非硅酸盐铁的分布遵循有机碳的分布:最大值仅限于表层,并沿剖面递减。研究表明,受侵蚀的农用黑钙土耕地层中粘土组分的MAOM中非硅酸盐铁含量的变化是侵蚀过程的结果,包括侵蚀强度,除其他外,侵蚀强度还取决于坡度。较低的坡度(4°)有助于增加氧化铁上的有机碳负载,从而增加铁的解吸能力,而较高的坡度(6°)则导致较低的铁解吸能力。建议将OC/Fed摩尔比作为土壤侵蚀程度的额外指标。在粘土组分中,无论其在土壤剖面中的位置还是在斜坡上的位置,有机物稳定的主要机制是形成有机铁络合物(OC/Fed>10)。在腐殖质层的残余部分中,非硅酸盐铁似乎主要以碳酸铁(FeCO3)的形式存在,而微团聚体(在超声处理下稳定)的比例(其中OM主要是胡敏素)相对较低,这是因为原生矿物在该部分中占绝对优势(重量%)。连二亚硫酸钠-柠檬酸盐-碳酸氢盐提取的矿物相关OM的大多数非硅酸盐铁位于粘土部分——2/3或更多。
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来源期刊
CiteScore
0.90
自引率
0.00%
发文量
15
审稿时长
8 weeks
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