Soil Organic Matter: II. Studies of the Origin and Chemical Structure of Soil Humic Acids

1961 ◽  
Vol 25 (1) ◽  
pp. 32-35 ◽  
Author(s):  
Harry H. Johnston
2006 ◽  
Vol 40 (3) ◽  
pp. 844-849 ◽  
Author(s):  
Abdul R. Khwaja ◽  
Paul R. Bloom ◽  
Patrick L. Brezonik

Agronomy ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1067
Author(s):  
Aleksandra Ukalska-Jaruga ◽  
Romualda Bejger ◽  
Guillaume Debaene ◽  
Bożena Smreczak

The objective of this paper was to investigate the molecular characterization of soil organic matter fractions (humic substances (HS): fulvic acids-FAs, humic acids-HAs, and humins-HNs), which are the most reactive soil components. A wide spectrum of spectroscopic (UV–VIS and VIS–nearIR), as well as electrochemical (zeta potential, particle size diameter, and polydispersity index), methods were applied to find the relevant differences in the behavior, formation, composition, and sorption properties of HS fractions derived from various soils. Soil material (n = 30) used for the study were sampled from the surface layer (0–30 cm) of agricultural soils. FAs and HAs were isolated by sequential extraction in alkaline and acidic solutions, according to the International Humic Substances Society method, while HNs was determined in the soil residue (after FAs and HAs extraction) by mineral fraction digestion using a 0.1M HCL/0.3M HF mixture and DMSO. Our study showed that significant differences in the molecular structures of FAs, Has, and HNs occurred. Optical analysis confirmed the lower molecular weight of FAs with high amount of lignin-like compounds and the higher weighted aliphatic–aromatic structure of HAs. The HNs were characterized by a very pronounced and strong condensed structure associated with the highest molecular weight. HAs and HNs molecules exhibited an abundance of acidic, phenolic, and amine functional groups at the aromatic ring and aliphatic chains, while FAs mainly showed the presence of methyl, methylene, ethenyl, and carboxyl reactive groups. HS was characterized by high polydispersity related with their structure. FAs were characterized by ellipsoidal shape as being associated to the long aliphatic chains, while HAs and HNs revealed a smaller particle diameter and a more spherical shape caused by the higher intermolecular forcing between the particles. The observed trends directly indicate that individual HS fractions differ in behavior, formation, composition, and sorption properties, which reflects their binding potential to other molecules depending on soil properties resulting from their type. The determined properties of individual HS fractions are presented as averaged characteristics over the examined soils with different physico-chemical properties.


2020 ◽  
Author(s):  
Ivan Alekseev ◽  
Evgeny Abakumov

<p>Polar soils play a key role in global carbon circulation and stabilization as they contain maximum stocks of soil organic matter (SOM) within the whole pedosphere. Cold climate and active layer dynamics result in the stabilization of essential amounts of organic matter in soils, biosediments, and grounds of the polar biome. Chemical composition of soil organic carbon (SOC) determines its decomposability and may affect soil organic matter stabilization (SOM) rate (Beyer, 1995). This is quite important for understanding variability in SOC pools and stabilization rate in context of changes in plant cover or climate (Rossi et al. 2016). <sup>13</sup>C nuclear magnetic resonance spectroscopy, which provides detailed information on diversity of structural composition of humic acids and SOM, may also be used to study the SOM dynamics under decomposition and humification proceses (Kogel-Knabner, 1997; Zech et al., 1997). This study aims to characterize molecular organization of the humic acids, isolated from various permafrost-affected soils of Yamal region and to assess the potential vulnerability of soils organic matter in context of possible mineralization processes. Organic carbon stocks for studied area were 7.85 ± 2.24 kg m-2 (for 0-10 cm layer), 14.97 ± 5.53 kg m-2 (for 0-30 cm), 23.99 ± 8.00 kg m-2 (for 0-100 cm). Results of solid-state 13C-NMR spectrometry showed low amounts of aromatic components in studied soils. All studied humic powders are characterized by predominance of aliphatic structures, and also carbohydrates, polysaccharides, ethers and amino acids. High content of aliphatic fragments in studied humic acids shows their similarity fulvic acids. Low level of aromaticity reflects the accumulation in soil of lowly decomposed organic matter due to cold temperatures. Our results provide further evidence of high vulnerability and sensitivity of permafrost-affected soils organic matter to Arctic warming. Consequently, these soils may play a crucial role in global carbon balance under effects of climate warming.</p>


1998 ◽  
Vol 38 (7) ◽  
pp. 667 ◽  
Author(s):  
J. O. Skjemstad ◽  
L. J. Janik ◽  
J. A. Taylor

Summary. Non-living soil organic matter is a small but critical component of soils contributing to soil structure, fertility and a range of other chemical, physical and biological functions. Although considerable work has contributed to our knowledge of its distribution, chemical structure, mineral associations and turnover, there is still little information on which fractions or pools of non-living soil organic matter are implicated in various soil functions and to what extent. This review paper summarises some of what is known about the distribution, chemistry, mineral associations and soil structure, turnover and the measurement of non-living soil organic matter, with particular emphasis on Australia. It also discusses some of the difficulties in using current methods for describing the function of this material in soil.


Geoderma ◽  
1975 ◽  
Vol 14 (4) ◽  
pp. 331-340 ◽  
Author(s):  
Khaled Y. Khalaf ◽  
Patrick MacCarthy ◽  
T.W. Gilbert

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