Soil organic matter

Last updated
Soil Organic Matter
SOM
Organic soil component
Profile Surface horizon, humus layer
Key minerals Carbon-rich compounds, lignin, cellulose
Key process Decomposition, humification
Parent materialPlant and animal detritus, microbial biomass
ClimateVariable, higher in cooler and wetter regions
pH Typically 5.5 – 7.0
O (organic), A (topsoil)
Primary Carbon (C), Nitrogen (N), Phosphorus (P), micronutrients
SecondaryMinerals, microbial by-products

Soil organic matter (SOM) is the organic matter component of soil, consisting of plant and animal detritus at various stages of decomposition, cells and tissues of soil microbes, and substances that soil microbes synthesize. SOM provides numerous benefits to soil's physical and chemical properties and its capacity to provide regulatory ecosystem services. [1] SOM is especially critical for soil functions and quality. [2]

Contents

The benefits of SOM result from several complex, interactive, edaphic factors; a non-exhaustive list of these benefits to soil function includes improvement of soil structure, aggregation, water retention, soil biodiversity, absorption and retention of pollutants, buffering capacity, and the cycling and storage of plant nutrients. SOM increases soil fertility by providing cation exchange sites and being a reserve of plant nutrients, especially nitrogen (N), phosphorus (P), and sulfur (S), along with micronutrients, which the mineralization of SOM slowly releases. As such, the amount of SOM and soil fertility are significantly correlated. [3]

SOM also acts as a major sink and source of soil carbon (C). Although the C content of SOM varies considerably, [4] [5] SOM is ordinarily estimated to contain 58% C, and "soil organic carbon" (SOC) is often used as a synonym for SOM, with measured SOC content often serving as a proxy for SOM. Soil represents one of the largest C sinks on Earth and is significant in the global carbon cycle and, therefore, for climate change mitigation. [6] Therefore, SOM/SOC dynamics and the capacity of soils to provide the ecosystem service of carbon sequestration through SOM management have received considerable attention. [7]

The concentration of SOM in soils generally ranges from 1% to 6% of the total mass of topsoil for most upland soils. Soils whose upper horizons consist of less than 1% of organic matter are mainly limited to deserts, while the SOM content of soils in low-lying, wet areas can be as great as 90%. Soils containing 12% to 18% SOC are generally classified as organic soils. [8]

SOM can be divided into three genera: the living biomass of microbes, fresh and partially decomposed detritus, and humus. Surface plant litter, i.e., fresh vegetal residue, is generally excluded from SOM. [9]

Sources

The primary source of SOM is vegetal detritus. In forests and prairies, for example, different soil organisms decompose the fresh detritus into simpler compounds. This involves several stages, the first being primarily mechanical and becoming more chemical as decomposition progresses. The microbial decomposers are included in the SOM and form a food web of organisms that prey upon each other and subsequently become prey.

Above detritivores, there are also herbivores that consume fresh vegetal matter, the residue of which then passes to the soil. The products of the metabolisms of these organisms are the secondary sources of SOM, which also includes their corpses. Some animals, like earthworms, termites, ants, and millipedes contribute to both vertical and horizontal translocation of organic matter. [1]

Additional sources of SOM include plant root exudates [10] and charcoal. [11]

Plant residue

Typical types and percentages of plant residue components
  1. Cellulose (45.0%)
  2. Lignin (20.0%)
  3. Hemicellulose (18.0%)
  4. Protein (8.00%)
  5. Sugars and starches (5.00%)
  6. Fats and waxes (2.00%)

Decomposition

Vegetal detritus generally is not soluble in water and, therefore, is inaccessible to plants. It constitutes, nevertheless, the raw matter from which plant nutrients derive. Soil microbes decompose it through enzymatic biochemical processes, obtain the necessary energy from the same matter, and produce the mineral compounds that plant roots are apt to absorb. [12] The decomposition of organic compounds specifically into mineral, i.e. inorganic, compounds, is denominated "mineralization". A portion of organic matter is not mineralized and instead decomposed into stable organic matter that is denominated "humus". [1]

The decomposition of organic compounds occurs at very different rates, depending on the nature of the compound. The ranking, from fast to slow rates, is:

  1. Sugars, starches, and simple proteins
  2. Proteins
  3. Hemicelluloses
  4. Cellulose
  5. Lignins and fats
  6. Chitin and waxes

The reactions that occur can be included in one of three genera:

The mineral products are:

ElementMineral Products
CarbonCO2, CO32−, HCO3, CH4, C
NitrogenNH4+, NO2, NO3, N2 (gas), N2O (gas)
SulfurS, H2S, SO32−, SO42−, CS2
PhosphorusH2PO4, HPO42−
OthersH2O, O2, H2, H+, OH, K+, Ca2+, Mg2+, etc.

Cellulose and hemicellulose undergo fast decomposition by fungi and bacteria, with a half-life of 12–18 days in a temperate climate. [13] Brown rot fungi can decompose the cellulose and hemicellulose, leaving the lignin and phenolic compounds behind. [14] Starch, which is an energy storage system for plants, undergoes fast decomposition by bacteria and fungi. [15] Lignin consists of polymers composed of 500 to 600 units with a highly branched, amorphous structure, linked to cellulose, hemicellulose and pectin in plant cell walls. [16] Lignin undergoes very slow decomposition, mainly by white rot fungi and actinomycetes; its half-life under temperate conditions is about six months. [13]

Lignin is resistant to breakdown and accumulates within the soil. It also reacts with proteins, [17] which further increases its resistance to decomposition, including enzymatic decomposition by microbes. [18] Fats and waxes from plant matter have still more resistance to decomposition and persist in soils for thousand years, hence their use as tracers of past vegetation in buried soil layers. [19] Clay soils often have higher organic contents that persist longer than soils without clay as the organic molecules adhere to and are stabilised by the clay. [20] Proteins normally decompose readily, to the exception of scleroproteins, but when bound to clay particles they become more resistant to decomposition. [21] As for other proteins clay particles absorb the enzymes exuded by microbes, decreasing enzyme activity while protecting extracellular enzymes from degradation. [22] The addition of organic matter to clay soils can render that organic matter and any added nutrients inaccessible to plants and microbes for many years. [23] A study showed increased soil fertility following the addition of mature compost to a clay soil. [24] High soil tannin content can cause nitrogen to be sequestered as resistant tannin-protein complexes. [25] [26]

Humus

Humus refers to organic matter that has been decomposed by soil microflora and fauna to the point where it is resistant to further breakdown. [27] Humus usually constitutes only five percent of the soil or less by volume, but it is an essential source of nutrients and adds important textural qualities crucial to soil health and plant growth. [28] Humus also feeds arthropods, termites and earthworms which further improve the soil. [29] The end product, humus, is suspended in colloidal form in the soil solution and forms a weak acid that can attack silicate minerals by chelating their iron and aluminum atoms. [30] Humus has a high cation and anion exchange capacity that on a dry weight basis is many times greater than that of clay colloids. [31] It also acts as a buffer, like clay, against changes in pH and soil moisture. [32]

As vegetal detritus decomposes, some microbially resistant compounds are let undecayed, including modified lignins, oils, fats, and waxes. Secondly, some new compounds are synthesized, like polysaccharides and polyuronids. These compounds are the basis of humus. New reactions occur between these compounds and some proteins and other products that contain nitrogen, thus incorporating nitrogen and avoiding its mineralization. Other nutrients are also protected in this way from mineralization. [33]

Humus formation is a process dependent on the amount of plant material added each year and the type of base soil. Both are affected by climate and the type of organisms present. [34] Soils with humus can vary in nitrogen content but typically have 3 to 6 percent nitrogen. Raw organic matter, as a reserve of nitrogen and phosphorus, is a vital component affecting soil fertility. [35] Humus also absorbs water, and expands and shrinks between dry and wet states to a higher extent than clay, increasing soil porosity. [36] Humus is less stable than the soil's mineral constituents, as it is reduced by microbial decomposition, and over time its concentration diminishes without the addition of new organic matter. However, humus in its most stable forms may persist over centuries if not millennia. [37] Charcoal is a source of highly stable humus, called black carbon, [38] which had been used traditionally to improve the fertility of nutrient-poor tropical soils. This very ancient practice, as ascertained in the genesis of Amazonian dark earths, has been renewed and became popular under the name of biochar. It has been suggested that biochar could be used to sequester more carbon in the fight against the greenhouse effect. [39]

Humic substances

Humic substances are classified into three genera based on their solubility in acids and alkalis, and also according to their stability:

Humic acids and fulvic acids, which begin as raw organic matter, are important constituents of humus. After the death of plants, animals, and microbes, microbes begin to feed on the residues through their production of extra-cellular soil enzymes, resulting finally in the formation of humus. [40] As the residues break down, only molecules made of aliphatic and aromatic hydrocarbons, assembled and stabilized by oxygen and hydrogen bonds, remain in the form of complex molecular assemblages collectively called humus. [41] Humus is never pure in the soil, because it reacts with metals and clays to form complexes which further contribute to its stability and to soil structure. [32] Although the structure of humus has in itself few nutrients (with the exception of constitutive metals such as calcium, iron and aluminum) it is able to attract and link, by weak chemical bonds, cation and anion nutrients that can further be released into the soil solution in response to selective root uptake and changes in soil pH, a process of paramount importance for the maintenance of fertility in tropical soils. [42]

Function in carbon cycling

Soil has a crucial function in the global carbon cycle, with the global soil carbon pool estimated to be 2,500 gigatons. This is 3.3 times the amount of the atmospheric pool at 750 gigatons and 4.5 times the biotic pool at 560 gigatons. The pool of organic carbon, which occurs primarily in the form of SOM, accounts for approximately 1,550 gigatons of the total global carbon pool, [43] [44] with soil inorganic carbon (SIC) accounting for the remainder. The pool of organic carbon exists in dynamic equilibrium between gains and losses; soil may therefore serve as either a sink or source of carbon through carbon sequestration or greenhouse gas emissions, respectively, depending on exogenous factors. [45]

Climatological influence

The production, accumulation and degradation of organic matter are greatly dependent on climate. For example, when a thawing event occurs, the flux of soil gases with atmospheric gases is significantly influenced. [46] Temperature, soil moisture and topography are the major factors affecting the accumulation of organic matter in soils. Organic matter tends to accumulate under wet or cold conditions where decomposer activity is impeded by low temperature [47] or excess moisture which results in anaerobic conditions. [48] Conversely, excessive rain and high temperatures of tropical climates enables rapid decomposition of organic matter and leaching of plant nutrients. Forest ecosystems on these soils rely on efficient recycling of nutrients and plant matter by the living plant and microbial biomass to maintain their productivity, a process which is disturbed by human activities. [49] Excessive slope, in particular in the presence of cultivation for the sake of agriculture, may encourage the erosion of the top layer of soil which holds most of the raw organic material that would otherwise eventually become humus. [50]

See also

References

  1. 1 2 3 4 5 6 7 Brady, Nyle C. (1984). The nature and properties of soils (9th ed.). London, United Kingdom: Macmillan. ISBN   978-0029460306 . Retrieved 27 November 2025.
  2. Beare, Mike H.; Cabrera, Miguel L.; Hendrix, Paul F.; Coleman, David C. (May–June 1994). "Aggregate-protected and unprotected organic matter pools in conventional and no-tillage soils". Soil Science Society of America Journal . 58 (3): 787–95. Bibcode:1994SSASJ..58..787B. doi:10.2136/sssaj1994.03615995005800030021x . Retrieved 27 November 2025.
  3. Tiessen, Holm; Cuevas, Elvira; Chacón, Prudencio (27 October 1994). "The role of soil organic matter in sustaining soil fertility". Nature . 371 (6500): 783–5. Bibcode:1994Natur.371..783T. doi:10.1038/371783a0 . Retrieved 27 November 2025.
  4. Périé, Catherine; Ouimet, Rock (May 2008). "Organic carbon, organic matter and bulk density relationships in boreal forest soils". Canadian Journal of Soil Science . 88 (3): 315–25. doi: 10.4141/CJSS06008 .
  5. Jain, Terri; Graham, Russell T.; Adams, David L. (July–August 1997). "Carbon to organic matter ratios for soils in Rocky Mountain coniferous forests". Soil Science Society of America Journal . 61 (4): 1190–5. Bibcode:1997SSASJ..61.1190J. doi:10.2136/sssaj1997.03615995006100040026x . Retrieved 27 November 2025.
  6. "Restoring soils could remove up to '5.5bn tonnes' of greenhouse gases every year". Carbon Brief . London, United Kingdom. 16 March 2020. Retrieved 27 November 2025.
  7. Ontl, Todd A.; Schulte, Lisa A. (2012). "Soil carbon storage". The Nature Education Knowledge Project. Cambridge, Massachusetts. Retrieved 27 November 2025.
  8. "Organic matter in soil: overview of composition, distribution, and content". Ocean Agro LLC. Nandesari Vadodara, India. 2018. Retrieved 27 November 2025.
  9. Bot, Alexandra; Benites, José (2005). "The importance of soil organic matter: key to drought-resistant soil and sustained food production. Chapter 1. Introduction". Food and Agriculture Organization of the United Nations . Rome, Italy. Retrieved 27 November 2025.
  10. Mergel, A.; Timchenko, A.; Kudeyarov, V. (1998). "Role of plant root exudates in soil carbon and nitrogen transformation". In Box, James E. Jr. (ed.). Root demographics and their efficiencies in sustainable agriculture, grasslands and forest ecosystems. Developments in plant and soil sciences. Vol. 82. Dordrecht, The Netherlands: Springer. pp. 43–54. doi:10.1007/978-94-011-5270-9_3. ISBN   978-94-010-6218-3 . Retrieved 27 November 2025.
  11. Skjemstad, Jan O.; Reicosky, Donald C.; Wilts, Alan R.; McGowan, Janine A. (2002). "Charcoal carbon in U.S. agricultural soils". Soil Science Society of America Journal . 66 (4): 1249–55. Bibcode:2002SSASJ..66.1249S. doi:10.2136/sssaj2002.1249 . Retrieved 27 November 2025.
  12. Ochoa-Hueso, Raul; Delgado-Baquerizo, Manuel; King, Paul T. A.; Benham, Merryn; Arca, Valentina; Power, Sally Ann (February 2019). "Ecosystem type and resource quality are more important than global change drivers in regulating early stages of litter decomposition". Soil Biology and Biochemistry . 129: 144–52. Bibcode:2019SBiBi.129..144O. doi:10.1016/j.soilbio.2018.11.009. hdl: 10261/336676 . S2CID   92606851 . Retrieved 27 November 2025.
  13. 1 2 Paul, Eldor A.; Paustian, Keith H.; Elliott, Edward T.; Cole, C. Vernon (1997). Soil organic matter in temperate agroecosystems: long-term experiments in North America. Boca Raton, Florida: CRC Press. p. 80. ISBN   978-0-8493-2802-2 . Retrieved 25 November 2025.
  14. Green, Frederick III; Highley, Terry L. (1997). "Mechanism of brown-rot decay: paradigm or paradox". International Biodeterioration and Biodegradation . 39 (2–3): 113–24. doi:10.1016/S0964-8305(96)00063-7 . Retrieved 25 November 2025.
  15. Adu, J. K.; Oades, J. Malcolm (1978). "Utilization of organic materials in soil aggregates by bacteria and fungi". Soil Biology and Biochemistry . 10 (2): 117–22. doi:10.1016/0038-0717(78)90081-0 . Retrieved 25 November 2025.
  16. Heredia, Antonia; Jiménez, Ana; Guillén, Rafael (January 1995). "Composition of plant cell walls". Zeitschrift für Lebensmittel-Untersuchung und Forschung. 200 (1): 24–31. doi:10.1007/BF01192903 . Retrieved 25 November 2025.
  17. Heck, Tobias; Faccio, Greta; Richter, Michael; Thöny-Meyer, Linda (25 November 2012). "Enzyme-catalyzed protein crosslinking". Applied Microbiology and Biotechnology . 97 (2): 461–75. doi: 10.1007/s00253-012-4569-z . PMC   3546294 . PMID   23179622.
  18. Lynch, D. L.; Lynch, C. C. (24 May 1958). "Resistance of protein–lignin complexes, lignins and humic acids to microbial attack". Nature . 181 (4621): 1478–9. Bibcode:1958Natur.181.1478L. doi:10.1038/1811478a0. PMID   13552710. S2CID   4193782 . Retrieved 25 November 2025.
  19. Dawson, Lorna A.; Hillier, Stephen (May 2010). "Measurement of soil characteristics for forensic applications". Surface and Interface Analysis . 42 (5): 363–77. doi:10.1002/sia.3315. S2CID   54213404. Archived (PDF) from the original on 8 May 2021. Retrieved 25 November 2025.
  20. Manjaiah, Kanchikeri Math; Kumar, Sarvendra; Sachdev, M. S.; Sachdev, P.; Datta, Samar Chandra (10 April 2010). "Study of clay–organic complexes". Current Science . 98 (7): 915–21. Retrieved 25 November 2025.
  21. Theng, Benny K.G. (1982). "Clay-polymer interactions: summary and perspectives". Clays and Clay Minerals . 30 (1): 1–10. Bibcode:1982CCM....30....1T. CiteSeerX   10.1.1.608.2942 . doi:10.1346/CCMN.1982.0300101. S2CID   98176725 . Retrieved 25 November 2025.
  22. Tietjen, Todd; Wetzel, Robert G. (October 2003). "Extracellular enzyme-clay mineral complexes: enzyme adsorption, alteration of enzyme activity, and protection from photodegradation" (PDF). Aquatic Ecology. 37 (4): 331–9. Bibcode:2003AqEco..37..331T. doi:10.1023/B:AECO.0000007044.52801.6b. S2CID   6930871 . Retrieved 25 November 2025.
  23. Tahir, Shermeen; Marschner, Petra (April 2017). "Clay addition to sandy soil: influence of clay type and size on nutrient availability in sandy soils amended with residues differing in C/N ratio". Pedosphere . 27 (2): 293–305. Bibcode:2017Pedos..27..293T. doi:10.1016/S1002-0160(17)60317-5 . Retrieved 25 November 2025.
  24. Melero, Sebastiana; Madejón, Engracia; Ruiz, Juan Carlos; Herencia, Juan Francisco (April 2007). "Chemical and biochemical properties of a clay soil under dryland agriculture system as affected by organic fertilization". European Journal of Agronomy. 26 (3): 327–34. Bibcode:2007EuJAg..26..327M. doi:10.1016/j.eja.2006.11.004 . Retrieved 25 November 2025.
  25. Joanisse, Gilles D.; Bradley, Robert L.; Preston, Caroline M.; Bending, Gary D. (January 2009). "Sequestration of soil nitrogen as tannin–protein complexes may improve the competitive ability of sheep laurel (Kalmia angustifolia) relative to black spruce (Picea mariana)". New Phytologist . 181 (1): 187–98. Bibcode:2009NewPh.181..187J. doi: 10.1111/j.1469-8137.2008.02622.x . PMID   18811620.
  26. Fierer, Noah; Schimel, Joshua P.; Cates, Rex G.; Zou, Jiping (October 2001). "Influence of balsam poplar tannin fractions on carbon and nitrogen dynamics in Alaskan taiga floodplain soils". Soil Biology and Biochemistry . 33 (12–13): 1827–39. Bibcode:2001SBiBi..33.1827F. doi:10.1016/S0038-0717(01)00111-0 . Retrieved 25 November 2025.
  27. Ponge, Jean-François (August 2022). "Humus: dark side of life or intractable "aether"?". Pedosphere. 32 (4): 660–4. Bibcode:2022Pedos..32..660P. doi:10.1016/S1002-0160(21)60013-9 . Retrieved 24 November 2025.
  28. Pettit, Robert E. "Organic matter, humus, humate, humic acid, fulvic acid and humin: their importance in soil fertility and plant health" (PDF). Retrieved 24 November 2025.
  29. Ji, Rong; Kappler, Andreas; Brune, Andreas (1 August 2000). "Transformation and mineralization of synthetic 14C-labeled humic model compounds by soil-feeding termites". Soil Biology and Biochemistry . 32 (8–9): 1281–91. CiteSeerX   10.1.1.476.9400 . doi:10.1016/S0038-0717(00)00046-8 . Retrieved 24 November 2025.
  30. Drever, James I.; Vance, George F. (1994). "Role of soil organic acids in mineral weathering processes". In Pittman, Edward D.; Lewan, Michael D. (eds.). Organic acids in geological processes. Berlin, Germany: Springer. pp. 138–61. doi:10.1007/978-3-642-78356-2_6. ISBN   978-3-642-78356-2 . Retrieved 24 November 2025.
  31. Shoba, V. N.; Chudnenko, Konstantin V. (14 August 2014). "Ion exchange properties of humus acids". Eurasian Soil Science. 47 (8): 761–71. doi:10.1134/S1064229314080110 . Retrieved 24 November 2025.
  32. 1 2 Piccolo, Alessandro (1996). "Humus and soil conservation". In Piccolo, Alessandro (ed.). Humic substances in terrestrial ecosystems. Amsterdam, the Netherlands: Elsevier. pp. 225–64. doi:10.1016/B978-044481516-3/50006-2. ISBN   978-0-444-81516-3 . Retrieved 24 November 2025.
  33. Paul, Eldor A. (July 2016). "The nature and dynamics of soil organic matter: plant inputs, microbial transformations, and organic matter stabilization" (PDF). Soil Biology and Biochemistry . 98: 109–26. doi:10.1016/j.soilbio.2016.04.001 . Retrieved 27 November 2025.
  34. Ponge, Jean-François (July 2003). "Humus forms in terrestrial ecosystems: a framework to biodiversity". Soil Biology and Biochemistry . 35 (7): 935–45. Bibcode:2003SBiBi..35..935P. CiteSeerX   10.1.1.467.4937 . doi:10.1016/S0038-0717(03)00149-4. S2CID   44160220 . Retrieved 19 November 2025.
  35. Foth, Henry D. (1984). Fundamentals of soil science (PDF) (8th ed.). New York, New York: Wiley. p. 139. ISBN   978-0-471-52279-9. Archived (PDF) from the original on 12 November 2020. Retrieved 24 November 2025.
  36. Peng, Xinhua; Horn, Rainer (February 2007). "Anisotropic shrinkage and swelling of some organic and inorganic soils". European Journal of Soil Science. 58 (1): 98–107. Bibcode:2007EuJSS..58...98P. doi:10.1111/j.1365-2389.2006.00808.x . Retrieved 25 November 2025.
  37. Wang, Yang; Amundson, Ronald; Trumbmore, Susan (May 1996). "Radiocarbon dating of soil organic matter" (PDF). Quaternary Research . 45 (3): 282–8. Bibcode:1996QuRes..45..282W. doi:10.1006/qres.1996.0029. S2CID   73640995 . Retrieved 25 November 2025.
  38. Brodowski, Sonja; Amelung, Wulf; Haumaier, Ludwig; Zech, Wolfgang (15 April 2007). "Black carbon contribution to stable humus in German arable soils". Geoderma. 139 (1–2): 220–8. Bibcode:2007Geode.139..220B. doi:10.1016/j.geoderma.2007.02.004 . Retrieved 25 November 2025.
  39. Criscuoli, Irene; Alberti, Giorgio; Baronti, Silvia; Favilli, Filippo; Martinez, Cristina; Calzolari, Costanza; Pusceddu, Emanuela; Rumpel, Cornelia; Viola, Roberto; Miglietta, Franco (10 March 2014). "Carbon sequestration and fertility after centennial time scale incorporation of charcoal into soil". PLOS ONE . 9 (3) e91114. Bibcode:2014PLoSO...991114C. doi: 10.1371/journal.pone.0091114 . PMC   3948733 . PMID   24614647.
  40. Varadachari, Chandrika; Ghosh, Kunal (1984). "On humus formation". Plant and Soil . 77 (2): 305–13. Bibcode:1984PlSoi..77..305V. doi:10.1007/BF02182933. S2CID   45102095 . Retrieved 25 November 2025.
  41. Piccolo, Alessandro (2002). "The supramolecular structure of humic substances: a novel understanding of humus chemistry and implications in soil science". Advances in Agronomy. 75: 57–134. doi:10.1016/S0065-2113(02)75003-7. ISBN   978-0-12-000793-6 . Retrieved 21 November 2025.
  42. Mendonça, Eduardo S.; Rowell, David L. (1 November 1996). "Mineral and organic fractions of two oxisols and their influence on effective cation-exchange capacity". Soil Science Society of America Journal . 60 (6): 1888–92. Bibcode:1996SSASJ..60.1888M. doi:10.2136/sssaj1996.03615995006000060038x . Retrieved 25 November 2025.
  43. Batjes, Niels H. (June 1996). "Total carbon and nitrogen in the soils of the world". European Journal of Soil Science. 47 (2): 151–63. Bibcode:1996EuJSS..47..151B. doi:10.1111/j.1365-2389.1996.tb01386.x . Retrieved 27 November 2025.
  44. Batjes, Niels H. (May 2016). "Harmonized soil property values for broad-scale modelling (WISE30sec) with estimates of global soil carbon stocks". Geoderma. 269: 61–8. Bibcode:2016Geode.269...61B. doi:10.1016/j.geoderma.2016.01.034 . Retrieved 27 November 2025.
  45. Lal, Rattan (November 2004). "Soil carbon sequestration to mitigate climate change". Geoderma. 123 (1–2): 1–22. doi:10.1016/j.geoderma.2004.01.032 . Retrieved 27 November 2025.
  46. Kim, Dong Jim; Vargas, Rodrigo; Bond-Lamberty, Ben; Turetsky, Merritt R. (9 July 2012). "Effects of soil rewetting and thawing on soil gas fluxes: a review of current literature and suggestions for future research". Biogeosciences . 9 (7): 2459–83. Bibcode:2012BGeo....9.2459K. doi: 10.5194/bg-9-2459-2012 .
  47. Wagai, Rota; Mayer, Lawrence M.; Kitayama, Kanehiro; Knicker, Heike (30 September 2008). "Climate and parent material controls on organic matter storage in surface soils: a three-pool, density-separation approach". Geoderma. 147 (1–2): 23–33. Bibcode:2008Geode.147...23W. doi:10.1016/j.geoderma.2008.07.010 . Retrieved 25 November 2025.
  48. Minayeva, Tatiana Y.; Trofimov, Sergey Ya.; Chichagova, Olga A.; Dorofeyeva, E. I.; Sirin, Andrey A.; Glushkov, Igor V.; Mikhailov, N. D.; Kromer, Bernd (5 October 2008). "Carbon accumulation in soils of forest and bog ecosystems of southern Valdai in the Holocene". Biology Bulletin. 35 (5): 524–32. Bibcode:2008BioBu..35..524M. doi:10.1134/S1062359008050142. S2CID   40927739 . Retrieved 25 November 2025.
  49. Vitousek, Peter M.; Sanford, Robert L. (November 1986). "Nutrient cycling in moist tropical forest". Annual Review of Ecology and Systematics . 17 (1): 137–67. Bibcode:1986AnRES..17..137V. doi:10.1146/annurev.es.17.110186.001033. S2CID   55212899 . Retrieved 25 November 2025.
  50. Rumpel, Cornelia; Chaplot, Vincent; Planchon, Olivier; Bernadou, J.; Valentin, Christian; Mariotti, André (31 January 2006). "Preferential erosion of black carbon on steep slopes with slash and burn agriculture". Catena. 65 (1): 30–40. Bibcode:2006Caten..65...30R. doi:10.1016/j.catena.2005.09.005 . Retrieved 25 November 2025.