Soil organic matter in soils of the Russian Arctic: insights from 13C-NMR spectroscopy

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>

Separations ◽  
2021 ◽  
Vol 8 (6) ◽  
pp. 87
Author(s):  
Vyacheslav Polyakov ◽  
Evgeny Abakumov

In the Arctic zone, where up to 1024 × 1013 kg of organic matter is stored in permafrost-affected soils, soil organic matter consists of about 50% humic substances. Based on the analysis of the molecular composition of humic acids, we assessed the processes of accumulation of the key structural fragments, their transformations and the stabilization rates of carbon pools in soils in general. The landscape of the Lena River delta is the largest storage of stabilized organic matter in the Arctic. There is active accumulation and deposition of a significant amount of soil organic carbon from terrestrial ecosystems in a permafrost state. Under ongoing climate change, carbon emission fluxes into the atmosphere are estimated to be higher than the sequestration and storing of carbon compounds. Thus, investigation of soil organic matter stabilization mechanisms and rates is quite an urgent topic regarding polar soils. For study of molecular elemental composition, humic acids were separated from the soils of the Lena River delta. Key structural fragments of humic matter were identified and quantified by CP/MAS 13C NMR spectroscopy: carboxyl (–COOR); carbonyl (–C=O); CH3–; CH2–; CH-aliphatic; –C-OR alcohols, esters and carbohydrates; and the phenolic (Ar-OH), quinone (Ar = O) and aromatic (Ar–) groups as benchmark Cryosols of the Lena delta river terrestrial ecosystem. Under the conditions of thermodynamic evolutionary selection, during the change between the dry and wet seasons, up to 41% of aromatic and carboxyl fragments accumulated in humic acids. Data obtained showed that three main groups of carbon played the most important role in soil organic matter stabilization, namely C, H-alkyls ((CH2)n/CH/C and CH3), aromatic compounds (C-C/C-H, C-O) and an OCH group (OCH/OCq). The variations of these carbon species’ content in separated humics, with special reference to soil–permafrost organic profiles’ recalcitrance in the current environment, is discussed.


Agronomy ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 2553
Author(s):  
Magdalena Banach-Szott ◽  
Andrzej Dziamski ◽  
Maciej Markiewicz

The still-advancing soil degradation and the related losses of soil organic carbon stocks due to the limited inflow of organic residues in agro-ecosystems encourage more and more soil protection. Establishing meadow ecosystems is one of the key methods of agricultural land use preventing losses of organic carbon in soils. Based on the research on the properties of humic acids, it is possible to determine the advancement of the processes of transformation and decomposition of soil organic matter. The obtained results may allow for the development of a soil protection strategy and more effective sequestration of organic carbon. Therefore, the aim of the research was to determine the properties of humic acids defining the quality of organic matter of meadow soils irrigated for 150 years with the slope-and-flooding system. The research was performed based on the soils (Albic Brunic Arenosol) sampled from Europe’s unique complex of permanent irrigated grasslands (the same irrigation management for 150 years), applying the slope-and-flooding system: the Czerskie Meadows. The soil samples were assayed for the content of total organic carbon (TOC) and the particle size distribution. HAs were extracted with the Schnitzer method and analysed for the elemental composition, spectrometric parameters in the UV-VIS (ultraviolet-visible) range, hydrophilic and hydrophobic properties and the infrared spectra. The research results showed that the HAs properties depend on the depth and the distance from the irrigation ditch. The HAs of soils sampled from the depth of 0–10 cm were identified with a lower “degree of maturity” as compared with the HAs of soils sampled from the depth of 20–30 cm, reflected by the values of atomic ratios (H/C, O/C, O/H), absorbance coefficients, and the FT-IR (Fourier transform infrared) spectra. The mean values of the H/C ratio in the HAs molecules of soils sampled from the depth of 20–30 cm were lower by 8.2% than those from the depth of 0–10 cm. The mean values of the absorbance coefficient A4/6 in the HAs molecules of soils sampled from the depth of 20–30 cm were lower by 9.6% than in the HAs molecules of soils sampled from the depth of 0–10 cm. The HAs molecules of the soils sampled 25 m from the irrigation ditch were identified with a higher degree of humification, as compared with the HAs of the soils sampled 5 m from the irrigation ditch. The results identified that humic acids produced in the many-year irrigated sandy soils were identified with a high degree of humification, which proves the relative stability of the soil’s organic matter. It confirms the importance of meadow soils for the carbon sequestration process. It should also be emphasized that the research area is interesting, although hardly described in terms of organic matter properties. Further and more detailed applicable research is planned, e.g., monitoring of total organic carbon content and comparing the properties of irrigated and non-irrigated meadow soils. Continuity of research is necessary to assess the direction of the soil organic matter transformation in such a unique ecosystem. The obtained results may allow for the development of, inter alia, models of agricultural practices that increase carbon sequestration in soils. In the long term, this will allow for greater environmental benefits and, thus, also increased financial benefits.


2011 ◽  
Vol 8 (6) ◽  
pp. 589 ◽  
Author(s):  
Michael Tatzber ◽  
Franz Mutsch ◽  
Axel Mentler ◽  
Ernst Leitgeb ◽  
Michael Englisch ◽  
...  

Environmental contextAnalysis of soil organic matter is important for understanding turnover and stabilisation processes of organic carbon in soils. Capillary electrophoresis is used here to investigate humic acids from soils of diverse forest sites, and show that the patterns of signals are indicative of soil characteristics. The method provides useful information of soil types and complements the existing set of methods for humic acid characterisation. AbstractAnalyses of humic substances provide very useful information about turnover characteristics and stabilisation processes of soil organic matter in environmental soil samples. The present study investigates 113 samples of forest soils from three different layers (undecomposed litter (L), if present, mixed samples of F (intermediate decomposed) and H (highly decomposed) organic matter (FH) and upper mineral soil layers (Ah horizon) from 0 to 5 cm) by extracting humic acids (HAs) and recording electropherograms. Five signals of these electropherograms were evaluated and correlated with basic parameters from soil (organic carbon, Corg, and total nitrogen, Nt, and extraction yields of HAs) and HAs (total carbon, Ct, and Nt), and with signals from photometry, mid-infrared and fluorescence spectroscopy. The developed method was able to separate HAs from different soil layers by calculating a discriminant function based on the five evaluated electrophoretic signals. The dataset of this work opened the opportunity to correlate the observed electrophoretic signals with the other determined soil parameters and spectroscopic signals. This can be seen as a very important step in the direction to assignments of the obtained electrophoretic signals. Soil characteristics were reflected quite well by this method and, combined with the other approaches, it is suitable for applications in further studies.


Solid Earth ◽  
2018 ◽  
Vol 9 (6) ◽  
pp. 1329-1339 ◽  
Author(s):  
Evgeny Abakumov ◽  
Ivan Alekseev

Abstract. Previously, the structure and molecular composition of the Antarctic soil organic matter (SOM) has been investigated using 13C-NMR methods, which showed that in typical organo-mineral soils the aliphatic carbon prevails over the aromatic one, owing to the non-ligniferous nature of its precursor material. In this study, the SOM was analysed from different sample areas (surface level and partially isolated supra-permafrost layer) of the tundra-barren landscape of the Fildes Peninsula, King George Island, Western Antarctica. We found that the humic acids (HAs) of the cryoturbated, buried areas had lower amounts of alkyl aromatic and protonized aromatic compounds. In contrast, the HAs from the surface layers contain less alkyl carbon components. The free-radical content was higher in the surface layers than in the buried layers due to the presence of fresh organic remnants in superficial soil samples. New data on SOM quality from these two representative Cryosols will enable a more precise assessment of SOM stabilization rate in sub-Antarctic tundras. Comparison of the 13C-NMR spectra of the HAs and the bulk SOM revealed that humification occurs in the Antarctic and results in accumulation of aromatic and carboxylic compounds and reductions in alkylic ones. This indicates that humification is one of the ways of soil organic matter stabilization.


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.


2021 ◽  
Vol 770 ◽  
pp. 145307
Author(s):  
Mohammad Bahadori ◽  
Chengrong Chen ◽  
Stephen Lewis ◽  
Sue Boyd ◽  
Mehran Rezaei Rashti ◽  
...  

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