scholarly journals From fibrous plant residues to mineral-associated organic carbon – the fate of organic matter in Arctic permafrost soils

2020 ◽  
Vol 17 (13) ◽  
pp. 3367-3383
Author(s):  
Isabel Prater ◽  
Sebastian Zubrzycki ◽  
Franz Buegger ◽  
Lena C. Zoor-Füllgraff ◽  
Gerrit Angst ◽  
...  
Keyword(s):  
Organic Matter ◽  
Chemical Composition ◽  
Organic Carbon ◽  
The Arctic ◽  
Plant Residues ◽  
N Losses ◽  
Organic C ◽  
Arctic Soils ◽  
C Cycle ◽  
C Stock

Abstract. Permafrost-affected soils of the Arctic account for 70 % or 727 Pg of the soil organic carbon (C) stored in the northern circumpolar permafrost region and therefore play a major role in the global C cycle. Most studies on the budgeting of C storage and the quality of soil organic matter (OM; SOM) in the northern circumpolar region focus on bulk soils. Thus, although there is a plethora of assumptions regarding differences in terms of C turnover or stability, little knowledge is available on the mechanisms stabilizing organic C in Arctic soils besides impaired decomposition due to low temperatures. To gain such knowledge, we investigated soils from Samoylov Island in the Lena River delta with respect to the composition and distribution of organic C among differently stabilized SOM fractions. The soils were fractionated according to density and particle size to obtain differently stabilized SOM fractions differing in chemical composition and thus bioavailability. To better understand the chemical alterations from plant-derived organic particles in these soils rich in fibrous plant residues to mineral-associated SOM, we analyzed the elemental, isotopic and chemical composition of particulate OM (POM) and clay-sized mineral-associated OM (MAOM). We demonstrate that the SOM fractions that contribute with about 17 kg C m−3 for more than 60 % of the C stock are highly bioavailable and that most of this labile C can be assumed to be prone to mineralization under warming conditions. Thus, the amount of relatively stable, small occluded POM and clay-sized MAOM that currently accounts with about 10 kg C m−3 for about 40 % of the C stock will most probably be crucial for the quantity of C protected from mineralization in these Arctic soils in a warmer future. Using δ15N as a proxy for nitrogen (N) balances indicated an important role of N inputs by biological N fixation, while gaseous N losses appeared less important. However, this could change, as with about 0.4 kg N m−3 one third of the N is present in bioavailable SOM fractions, which could lead to increases in mineral N cycling and associated N losses under global warming. Our results highlight the vulnerability of SOM in Arctic permafrost-affected soils under rising temperatures, potentially leading to unparalleled greenhouse gas emissions from these soils.

scholarly journals From fibrous plant residues to mineral-associated organic carbon – the fate of organic matter in Arctic permafrost soils

2020 ◽  
Author(s):  
Isabel Prater ◽  
Sebastian Zubrzycki ◽  
Franz Buegger ◽  
Lena C. Zoor-Füllgraff ◽  
Gerrit Angst ◽  
...  
Keyword(s):  
Organic Matter ◽  
Chemical Composition ◽  
Organic Carbon ◽  
The Arctic ◽  
Plant Residues ◽  
N Losses ◽  
Organic C ◽  
Arctic Soils ◽  
C Cycle ◽  
C Stock

Abstract. Permafrost-affected soils of the Arctic account for 70 % or 727 Pg of the soil organic carbon (C) stored in the permafrost region and therefore play a major role in the global C cycle. Most studies on the budgeting of C storage and the quality of soil organic matter (SOM) in the northern circumpolar region focus on bulk soils. Thus, although there is a plethora of assumptions regarding differences in terms of C turnover or stability, only little knowledge is available on the mechanisms stabilizing organic C in Arctic soils besides impaired decomposition due to low temperatures. To gain such knowledge, we investigated soils from Samoylov Island in the Lena River Delta with respect to the composition and distribution of organic C among differently stabilized SOM fractions. The soils were fractionated according to density and particle size to obtain differently stabilized SOM fractions differing in chemical composition and thus bioavailability. To better understand the chemical alterations from plant-derived organic particles in these soils rich in fibrous plant residues to mineral-associated SOM, we analysed the elemental, isotopic and chemical composition of particulate OM (POM) and clay-sized mineral-associated OM (MAOM). We demonstrate that the SOM fractions that contribute with about 17 kg C m−3 for more than 60 % of the C stock are highly bioaccessible and that most of this labile C can be assumed to be prone to mineralization under warming conditions. Thus, the amount of relatively stable, small occluded POM and clay-sized MAOM that account currently with about 10 kg C m−3 for about 40 % of the C stock will most probably be crucial for the quantity of C protected from mineralization in these Arctic soils in a warmer future. Using δ15N as proxy for nitrogen (N) balances indicated an important role of N inputs by biological N fixation, while gaseous N losses appeared less important. However, this could change, as with about 0.4 kg N m−3 one third of the N is present in bioaccessible SOM fractions, which could lead to increases in mineral N cycling and associated N losses under global warming. Our results highlight the vulnerability of SOM in Arctic permafrost-affected soils under rising temperatures, potentially leading to unparalleled greenhouse gas emissions from these soils.

The role of photodegradation on the mineralization of permafrost DOM

2020 ◽  
Author(s):  
Flora Mazoyer ◽  
Isabelle Laurion ◽  
Milla Rautio
Keyword(s):  
Organic Matter ◽  
Organic Carbon ◽  
Light Attenuation ◽  
Community Response ◽  
Water Bodies ◽  
The Arctic ◽  
Carbon Pools ◽  
Dark Incubation ◽  
Arctic Soils ◽  
Bacterial Inoculum

<p>Permafrost thaw leads to the formation of shallow water bodies in which large quantities of terrestrial organic carbon are mobilized as dissolved organic matter (DOM), partly turned into greenhouse gases (GHG). DOM comes from ancient carbon pools trapped in frozen soils for hundreds to thousands of years but also from present-day primary producers. Determining the fate of these pools is fundamental to evaluate the potential of these water bodies to amplify climate warming through their GHG emissions. In addition to the microbial degradation pathways producing CO<sub>2</sub> and CH<sub>4</sub>, DOM can be directly mineralized into CO<sub>2</sub> by sunlight. The CO<sub>2</sub> production rates from photodegradation vary extensively across Arctic regions. The controlling factors and interactions with the microbial communities are not well understood, while photodegradation is likely to rise as the open-water season extends. Determining the photo- and bio-lability of the carbon pools available on thawing permafrost landscapes is needed to predict to what extent these systems can affect the global carbon cycle.</p><p>Various DOM and environmental characteristics are considered in my PhD project, including mixing regime, seasonal exposure and light attenuation, as well as the microbial community response to photo-induced chemistry changes in DOM. Study sites include subarctic and arctic peatland areas of Eastern Canada, rich in thaw ponds and where organic matter started to accumulate between 3700 and 5600 years BP. These are non-Yedoma systems that have been poorly studied despite the large amount of organic carbon they store. This presentation will show the results of a lab experiment using a solar simulator where DOM of various origins and ages were tested: thaw pond water and leachates from plants, permafrost active layer, and previously unthawed permafrost. Short term incubations were carried out under five treatments: exposure to light without bacteria (0.2 µm filtration), exposure to light followed by a dark incubation with a bacterial inoculum, dark incubation with a bacterial inoculum, dark incubation with the whole bacterial community (2.7 µm filtration), and dark control without bacteria. A set of optical, biological and chemical characteristics were measured at the beginning and end of incubation. DOM losses (DOC, CDOM, and FDOM) and CO<sub>2</sub> production vary extensively among treatments and DOM pools. They were the highest in dark bacterial incubations of plants leachates. DOM of the subarctic area was quite refractory to degradation in general, except for the biodegradation of the unthawed permafrost leachate (- 50%). Photodegradation was observed in all water types, with DOM losses faster than biodegradation ones for the Arctic soils leachates and all the ponds waters. The highest CO<sub>2</sub> photoproduction was measured in Arctic unthawed permafrost leachates. Finally, the enhancement of DOM lability to microbes caused by photodegradation was generally observed for unthawed permafrost leachates. Incoming biological and 14C data, along with multivariate analyses, will improve the characterisation of the trends.</p>

scholarly journals Long term trends in fertility of soils under continuous cultivation and cereal cropping in southern Queensland. III. Distribution and kinetics of soil organic carbon in particle size fractions

Soil Research ◽  
1986 ◽  
Vol 24 (2) ◽  
pp. 293 ◽  
Author(s):  
RC Dalal ◽  
RJ Mayer
Keyword(s):  
Particle Size ◽  
Organic Matter ◽  
Organic Carbon ◽  
Soil Organic Carbon ◽  
Size Fraction ◽  
Organic C ◽  
Size Fractions ◽  
Particle Size Fractions ◽  
Clay Size Fraction ◽  
Sand Size

Distribution of soil organic carbon in sand-, silt- and clay-size fractions during cultivation for periods ranging from 20 to 70 years was studied in six major soils used for cereal cropping in southern Queensland. Particle-size fractions were obtained by dispersion in water using cation exchange resin, sieving and sedimentation. In the soils' virgin state no single particle-size fraction was found to be consistently enriched as compared to the whole soil in organic C in all six soils, although the largest proportion (48%) of organic C was in the clay-size fraction; silt and sand-size fractions contained remaining organic C in equal amounts. Upon cultivation, the amounts of organic C declined from all particle-size fractions in most soils, although the loss rates differed considerably among different fractions and from the whole soil. The proportion of the sand-size fraction declined rapidly (from 26% to 12% overall), whereas that of the clay-size fraction increased from 48% to 61% overall. The proportion of silt-size organic C was least affected by cultivation in most soils. It was inferred, therefore, that the sand-size organic matter is rapidly lost from soil, through mineralization as well as disintegration into silt-size and clay-size fractions, and that the clay fraction provides protection for the soil organic matter against microbial and enzymic degradation.

Soil organic carbon and nitrogen sequestration and turnover in aggregates under subtropical leucaena–grass pastures

Soil Research ◽  
2018 ◽  
Vol 56 (6) ◽  
pp. 632 ◽  
Author(s):  
Kathryn Conrad ◽  
Ram C. Dalal ◽  
Ryosuke Fujinuma ◽  
Neal W. Menzies
Keyword(s):  
Organic Matter ◽  
Organic Carbon ◽  
Soil Organic Carbon ◽  
Soil Aggregates ◽  
Soil Mass ◽  
Δ13c And Δ15n ◽  
Organic C ◽  
Carbon And Nitrogen ◽  
Nitrogen Sequestration ◽  
C And N

Stabilisation and protection of soil organic carbon (SOC) in macroaggregates and microaggregates represents an important mechanism for the sequestration of SOC. Legume-based grass pastures have the potential to contribute to aggregate formation and stabilisation, thereby leading to SOC sequestration. However, there is limited research on the C and N dynamics of soil organic matter (SOM) fractions in deep-rooted legume leucaena (Leucaena leucocephala)–grass pastures. We assessed the potential of leucaena to sequester carbon (C) and nitrogen (N) in soil aggregates by estimating the origin, quantity and distribution in the soil profile. We utilised a chronosequence (0–40 years) of seasonally grazed leucaena stands (3–6 m rows), which were sampled to a depth of 0.3 m at 0.1-m intervals. The soil was wet-sieved for different aggregate sizes (large macroaggregates, >2000 µm; small macroaggregates, 250–2000 µm; microaggregates, 53–250 µm; and <53 µm), including occluded particulate organic matter (oPOM) within macroaggregates (>250 µm), and then analysed for organic C, N and δ13C and δ15N. Leucaena promoted aggregation, which increased with the age of the leucaena stands, and in particular the formation of large macroaggregates compared with grass in the upper 0.2 m. Macroaggregates contained a greater SOC stock than microaggregates, principally as a function of the soil mass distribution. The oPOM-C and -N concentrations were highest in macroaggregates at all depths. The acid nonhydrolysable C and N distribution (recalcitrant SOM) provided no clear distinction in stabilisation of SOM between pastures. Leucaena- and possibly other legume-based grass pastures have potential to sequester SOC through stabilisation and protection of oPOM within macroaggregates in soil.

scholarly journals Permafrost-Affected Soils of the Russian Arctic and their Carbon Pools

2014 ◽  
Vol 6 (1) ◽  
pp. 619-655
Author(s):  
S. Zubrzycki ◽  
L. Kutzbach ◽  
E.-M. Pfeiffer
Keyword(s):  
Organic Matter ◽  
Organic Carbon ◽  
Soil Organic Carbon ◽  
Carbon Sink ◽  
Global Climate ◽  
Fundamental Property ◽  
Climate System ◽  
The Arctic ◽  
Quaternary Period ◽  
Permafrost Regions

Abstract. Permafrost-affected soils have accumulated enormous pools of organic matter during the Quaternary Period. The area occupied by these soils amounts to more than 8.6 million km2, which is about 27% of all land areas north of 50° N. Therefore, permafrost-affected soils are considered to be one of the most important cryosphere elements within the climate system. Due to the cryopedogenic processes that form these particular soils and the overlying vegetation that is adapted to the arctic climate, organic matter has accumulated to the present extent of up to 1024 Pg (1 Pg = 1015 g = 1 Gt) of soil organic carbon stored within the uppermost three meters of ground. Considering the observed progressive climate change and the projected polar amplification, permafrost-affected soils will undergo fundamental property changes. Higher turnover and mineralization rates of the organic matter are consequences of these changes, which are expected to result in an increased release of climate-relevant trace gases into the atmosphere. As a result, permafrost regions with their distinctive soils are likely to trigger an important tipping point within the global climate system, with additional political and social implications. The controversy of whether permafrost regions continue accumulating carbon or already function as a carbon source remains open until today. An increased focus on this subject matter, especially in underrepresented Siberian regions, could contribute to a more robust estimation of the soil organic carbon pool of permafrost regions and at the same time improve the understanding of the carbon sink and source functions of permafrost-affected soils.

scholarly journals Soil organic carbon stabilization mechanisms and temperature sensitivity in old terraced soils

2021 ◽  
Vol 18 (23) ◽  
pp. 6301-6312
Author(s):  
Pengzhi Zhao ◽  
Daniel Joseph Fallu ◽  
Sara Cucchiaro ◽  
Paolo Tarolli ◽  
Clive Waddington ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Soil Organic Carbon ◽  
Temperature Sensitivity ◽  
Land Surface ◽  
C:N Ratio ◽  
Temperature Sensitive ◽  
Organic C ◽  
Fraction Composition ◽  
Soil Burial ◽  
C Cycle

Abstract. Being the most common human-created landforms, terrace construction has resulted in an extensive perturbation of the land surface. However, our mechanistic understanding of soil organic carbon (SOC) (de-)stabilization mechanisms and the persistence of SOC stored in terraced soils is far from complete. Here we explored the factors controlling SOC stability and the temperature sensitivity (Q10) of abandoned prehistoric agricultural terrace soils in NE England using soil fractionation and temperature-sensitive incubation combined with terrace soil burial-age measurements. Results showed that although buried terrace soils contained 1.7 times more unprotected SOC (i.e., coarse particulate organic carbon) than non-terraced soils at comparable soil depths, a significantly lower potential soil respiration was observed relative to a control (non-terraced) profile. This suggests that the burial of former topsoil due to terracing provided a mechanism for stabilizing SOC. Furthermore, we observed a shift in SOC fraction composition from particulate organic C towards mineral-protected C with increasing burial age. This clear shift to more processed recalcitrant SOC with soil burial age also contributes to SOC stability in terraced soils. Temperature sensitivity incubations revealed that the dominant controls on Q10 depend on the terrace soil burial age. At relatively younger ages of soil burial, the reduction in substrate availability due to SOC mineral protection with aging attenuates the intrinsic Q10 of SOC decomposition. However, as terrace soil becomes older, SOC stocks in deep buried horizons are characterized by a higher temperature sensitivity, potentially resulting from the poor SOC quality (i.e., soil C:N ratio). In conclusion, terracing in our study site has stabilized SOC as a result of soil burial during terrace construction. The depth–age patterns of Q10 and SOC fraction composition of terraced soils observed in our study site differ from those seen in non-terraced soils, and this has implications when assessing the effects of climate warming and terrace abandonment on the terrestrial C cycle.

The effects of cultivation on the composition of organic-matter and structural stability of soils

Soil Research ◽  
1995 ◽  
Vol 33 (6) ◽  
pp. 975 ◽  
Author(s):  
A Golchin ◽  
P Clarke ◽  
JM Oades ◽  
JO Skjemstad
Keyword(s):  
Organic Matter ◽  
Chemical Composition ◽  
Organic Carbon ◽  
Organic Materials ◽  
Aggregate Stability ◽  
Soil Samples ◽  
Modulus Of Rupture ◽  
Dispersible Clay ◽  
Different Soils

Soil samples were obtained from the surface horizons of five untilled sites and adjacent sites under short- and long-term cultivation. The soil samples were fractionated based on density and organic materials were concentrated in various fractions which enabled comparative chemical composition of the organic materials in cultivated and uncultivated sites by solid-state C-13 CP/MAS NMR spectroscopy. Changes in the nature of organic carbon with cultivation were different in different soils and resulted from variations in the chemistry of carbon inputs to the soils and a greater extent of decomposition of organic materials in cultivated soils. Differences in the chemical composition of organic carbon between cultivated and uncultivated soils resided mostly in organic materials occluded within aggregates, whereas the chemistry of organic matter associated with clay particles showed only small changes. The results indicate a faster decomposition of O-alkyl C in the cultivated soils. Wet aggregate stability, mechanically dispersible clay and modulus of rupture tests were used to assess the effects of cultivation on structural stability of soils. In four of five soils, the virgin sites and sites which had been under long-term pasture had a greater aggregate stability than the cultivated sites. Neither total organic matter nor total O-alkyl C content was closely correlated with aggregate stability, suggesting that only a part of soil carbon or carbohydrate is involved in aggregate stability. The fractions of carbon and O-alkyl C present in the form of particulate organic matter occluded within aggregates were better correlated with aggregate stability (r = 0.86** and 0.88**, respectively). Cultivation was not the dominant factor influencing water-dispersible clay across the range of soil types used in this study. The amount of dispersible clay was a function of total clay content and the percentage of clay dispersed was controlled by factors such as clay mineralogy, CaCO3 and organic matter content of soils. The tendency of different soils for hard-setting and crusting, as a result of structural collapse, was reflected in the modulus of rupture (MOR). The cultivated sites had significantly higher MOR than their non-tilled counterparts. The soils studied had different MOR due to differences in their physical and chemical properties.

scholarly journals Evaluation of terrestrial pan-Arctic carbon cycling using a data-assimilation system

2019 ◽  
Vol 10 (2) ◽  
pp. 233-255 ◽  
Author(s):  
Efrén López-Blanco ◽  
Jean-François Exbrayat ◽  
Magnus Lund ◽  
Torben R. Christensen ◽  
Mikkel P. Tamstorf ◽  
...  
Keyword(s):  
The Arctic ◽  
Soil Organic C ◽  
Area Index ◽  
Organic C ◽  
Soil C ◽  
Transit Times ◽  
C Cycle ◽  
C Stocks ◽  
Data Assimilation System ◽  
Assimilation System

Abstract. There is a significant knowledge gap in the current state of the terrestrial carbon (C) budget. Recent studies have highlighted a poor understanding particularly of C pool transit times and of whether productivity or biomass dominate these biases. The Arctic, accounting for approximately 50 % of the global soil organic C stocks, has an important role in the global C cycle. Here, we use the CARbon DAta MOdel (CARDAMOM) data-assimilation system to produce pan-Arctic terrestrial C cycle analyses for 2000–2015. This approach avoids using traditional plant functional type or steady-state assumptions. We integrate a range of data (soil organic C, leaf area index, biomass, and climate) to determine the most likely state of the high-latitude C cycle at a 1∘ × 1∘ resolution and also to provide general guidance about the controlling biases in transit times. On average, CARDAMOM estimates regional mean rates of photosynthesis of 565 g C m−2 yr−1 (90 % confidence interval between the 5th and 95th percentiles: 428, 741), autotrophic respiration of 270 g C m−2 yr−1 (182, 397) and heterotrophic respiration of 219 g C m−2 yr−1 (31, 1458), suggesting a pan-Arctic sink of −67 (−287, 1160) g Cm−2 yr−1, weaker in tundra and stronger in taiga. However, our confidence intervals remain large (and so the region could be a source of C), reflecting uncertainty assigned to the regional data products. We show a clear spatial and temporal agreement between CARDAMOM analyses and different sources of assimilated and independent data at both pan-Arctic and local scales but also identify consistent biases between CARDAMOM and validation data. The assimilation process requires clearer error quantification for leaf area index (LAI) and biomass products to resolve these biases. Mapping of vegetation C stocks and change over time and soil C ages linked to soil C stocks is required for better analytical constraint. Comparing CARDAMOM analyses to global vegetation models (GVMs) for the same period, we conclude that transit times of vegetation C are inconsistently simulated in GVMs due to a combination of uncertainties from productivity and biomass calculations. Our findings highlight that GVMs need to focus on constraining both current vegetation C stocks and net primary production to improve a process-based understanding of C cycle dynamics in the Arctic.

Colloidal matter in water extracts from forest soils

2007 ◽  
Vol 4 (6) ◽  
pp. 424 ◽  
Author(s):  
Alexander Dreves ◽  
Nils Andersen ◽  
Pieter M. Grootes ◽  
Marie-Josée Nadeau ◽  
Carl-Dieter Garbe-Schönberg
Keyword(s):  
Organic Matter ◽  
Chemical Composition ◽  
Soil Water ◽  
Relative Proportion ◽  
Transport Processes ◽  
Total Charge ◽  
Dual Nature ◽  
Organic C ◽  
Water Extracts ◽  
Colloidal Fraction

Environmental context. Little is known about the proportion of tiny dispersed particles and true solutions in soil water although the distinction has a major influence on transport processes of organic matter, fertiliser and pollutants in soils and thus, e.g., on carbon storage, and its role in global warming. Our study has found a noticeable amount of tiny particles (range 17 nm to 1.0 μm) in filtered soil water, that have a different chemical composition and a lower bioavailability of their organic components in comparison to the soluble part. This significant occurrence and the ecological relevance of colloids for the transport and storage of soil constituents highlights the need to partition soil water content into ‘particulate’ and ‘dissolved’ since the access to soil pores determines particle transport. Abstract. Water-extracted organic matter (WEOM) is widely used as a surrogate for natural organic matter in soil water in the investigation of soil carbon dynamics. Information about the dissolved or colloidal nature of the organic matter is scarce since dissolved organic matter (DOM) is simply operationally defined by filtration: ‘DOM is what passes through the filter’. Water extracts of two topsoil horizons from both a deciduous (Steinkreuz) and a coniferous (Rotthalmünster) forest, located in Bavaria (Germany), were filtered through a 1-μm quartz filter and analysed regarding the amount of colloids in the range ~17 nm to 1.0 μm, the chemical composition and the radiocarbon concentration of both the colloidal and the dissolved fraction separated by high-speed centrifugation. Up to 13.9 wt-% of the total charge of the water extracts belongs to the colloidal fraction. The colloidal fraction has a higher relative proportion of metals and older organic C than the dissolved fraction. This demonstrates the dual nature of WEOM and the need for a more careful definition of DOM.

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