Soil carbon

Soil carbon includes both inorganic carbon as carbonate minerals, and as soil organic matter.[1] Soil carbon plays a key role in the carbon cycle, and thus it is important in global climate models.

Overview

Soil carbon is present in two forms: inorganic and organic. Soil inorganic carbon consists of mineral forms of C, either from weathering of parent material, or from reaction of soil minerals with atmospheric CO2. Carbonate minerals are the dominant form of soil carbon in desert climates. Soil organic carbon is present as soil organic matter. It includes relatively available C as fresh plant remains and relatively inert C in materials derived from plant remains: humus and charcoal.[2]

Global carbon cycle

See also: Carbon cycle

Of the 2,700 Gt of C stored in soils worldwide, 1550 GtC is organic and 950 GtC is inorganic carbon, which is approximately three times greater than the current atmospheric C and 240 times higher compared with the current annual fossil fuel emission.[3] The balance of soil carbon is held in peat and wetlands (150 GtC), and in plant litter at the soil surface (50 GtC). This compares to 780 GtC in the atmosphere, and 600 GtC in all living organisms. The oceanic pool holds 38,200 GtC.

About 60 GtC/yr is added to soil. This 60 GtC/yr is the balance of 120 GtC/yr taken out of the atmosphere by terrestrial plant photosynthesis reduced by 60 GtC/yr plant respiration. An equivalent 60 GtC/yr is respired from soil, joining the 60G tC/yr plant respiration to return to the atmosphere.[4][5]

Organic carbon

Soil organic carbon is divided between living soil biota and dead biotic material derived from biomass. Together these comprise the soil food web, with the living component sustained by the biotic material component. Soil biota includes earthworms, nematodes, protozoa, fungi, bacteria and different arthropods.

Detritus resulting from plant senescence is the major source of soil organic carbon. Plant materials, with cell walls high in cellulose and lignin, are decomposed and the not-respired carbon is retained as humus. Cellulose and starches are easily degraded, resulting in relatively short residence times. More persistent forms of organic C include lignin, humus, organic matter encapsulated in soil aggregates, and charcoal. These resist alteration and have long residence times.

Soil organic carbon tends to be concentrated in the topsoil. Topsoil ranges from 0.5% to 3.0% organic C for most upland soils. Soils with less than 0.5% organic C are mostly limited to desert areas. Soils containing greater than 12 - 18% organic C are generally classified as organic soils. High levels of organic C develop in soils supporting wetland ecology, flood deposition, fire ecology, and human activity.

Fire derived forms of carbon are present in most soils as unweathered charcoal and weathered black carbon.[6][7] Soil organic C is typically 5 - 50% derived from char,[8] with levels above 50% encountered in mollisol, chernozem, and terra preta soils.[9]

Root exudates are another source of soil carbon.[10] 5 - 20% of the total plant carbon fixed during photosynthesis is supplied as root exudates in support of rhizospheric mutualistic biota.[11][12] Microbial populations are typically higher in the rhizosphere than in adjacent bulk soil.

Soil health

A portable soil respiration system measuring soil CO2 flux
Main article: Soil health

Organic carbon is vital to soil capacity to provide edaphic ecosystem services. The condition of this capacity is termed soil health, a term that communicates the value of understanding soil as a living system as opposed to an abiotic component. Specific carbon related benchmarks used to evaluate soil health include CO2 release, humus levels, and microbial metabolic activity.

Losses

The exchange of carbon between soils and the atmosphere is a significant part of the world carbon cycle. Carbon, as it relates to the organic matter of soils, is a major component of soil and catchment health. Several factors affect the variation that exists in soil organic matter and soil carbon; the most significant has, in contemporary times, been the influence of humans and agricultural systems.

Although exact quantities are difficult to measure, human activities have caused massive losses of soil organic carbon.[13] First was the use of fire, which removes soil cover and leads to immediate and continuing losses of soil organic carbon. Tillage and drainage both expose soil organic matter to oxygen and oxidation. In the Netherlands, East Anglia, Florida, and the California Delta, subsidence of peat lands from oxidation has been severe as a result of tillage and drainage. Grazing management that exposes soil (through either excessive or insufficient recovery periods) can also cause losses of soil organic.

Managing soil carbon

Natural variations in SOM occur as a result of climate, organisms, parent material, time, and relief.[14] The greatest contemporary influence has been that of humans; for example, historical SOM in Australian agricultural soils may have been twice the present range that is typically from 1.6 to 4.6 per cent.[15]

It has long been encouraged that farmers adjust practices to maintain or increase the organic component in the soil. On one hand, practices that hasten oxidation of carbon (such as burning crop stubbles or over-cultivation) are discouraged; on the other hand, incorporation of organic material (such as in manuring) has been encouraged. Increasing soil carbon is not a straightforward matter; it is made complex by the relative activity of soil biota, which can consume and release carbon and are made more active by the addition of nitrogen fertilizers.[14]

Data available on soil organic carbon

Europe

The most homogeneous and comprehensive data on the organic carbon/matter content of European soils remain those that can be extracted and/or derived from the European Soil Database in combination with associated databases on land cover, climate, and topography. The modelled data refer to carbon content (%) in the surface horizon of soils in Europe. In an inventory on available national datasets, seven member states of the European Union have available datasets on organic carbon. In the article "Estimating soil organic carbon in Europe based on data collected through an European network" (Ecological Indicators 24, pp. 439–450), a comparison of national data with modelled data is performed. Finally, a new proposed model for estimation of soil organic carbon in agricultural soils has estimated current top SOC stock of 17.63 Gt in EU agricultural soils.

Managing for catchment health

Much of the contemporary literature on soil carbon relates to its role, or potential, as an atmospheric carbon sink to offset climate change. Despite this emphasis, a much wider range of soil and catchment health aspects are improved as soil carbon is increased. These benefits are difficult to quantify, due to the complexity of natural resource systems and the interpretation of what constitutes soil health; nonetheless, several benefits are proposed in the following points:

Forest soils

Forest soils constitute a large pool of carbon. Anthropogenic activities such as deforestation cause releases of carbon from this pool, which may significantly increase the concentration of greenhouse gas (GHG) in the atmosphere.[16] Under the United Nations Framework Convention on Climate Change (UNFCCC), countries must estimate and report GHG emissions and removals, including changes in carbon stocks in all five pools (above- and below-ground biomass, dead wood, litter, and soil carbon) and associated emissions and removals from land use, land-use change and forestry activities, according to the Intergovernmental Panel on Climate Change's good practice guidance.[17][18] Tropical deforestation represents nearly 25 percent of total anthropogenic GHG emissions worldwide.[19] Deforestation, forest degradation, and changes in land management practices can cause releases of carbon from soil to the atmosphere. For these reasons, reliable estimates of soil organic carbon stock and stock changes are needed for Reducing Emissions from Deforestation and Forest Degradation and GHG reporting under the UNFCCC.

The government of Tanzania—together with the Food and Agriculture Organization of the United Nations[20] and the financial support of the government of Finland—have implemented a forest soil carbon monitoring program[21] to estimate soil carbon stock, using both survey and modelling-based methods.

See also

References

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  2. Lal, R. (February 2007). "Carbon Management in Agricultural Soils". Mitigation and Adaption Strategies for Global Change. Springer. 12: 303–322. doi:10.1007/s11027-006-9036-7. Retrieved 16 January 2016.
  3. Balal Yousaf, Guijian Liu, Ruwei Wang, Qumber Abbas, Muhammad Imtiaz, Ruijia Liu: Investigating the biochar effects on C-mineralization and sequestration of carbon in soil compared with conventional amendments using stable isotope (δ13C) approach. GCB Bioenergy 2016; DOI: 10.1111/gcbb.12401
  4. Lal, Rattan (2008). "Sequestration of atmospheric CO2 in global carbon pools". Energy and Environmental Science. 1 (1): 86–100. doi:10.1039/b809492f. Retrieved 16 January 2016.
  5. "An Introduction to the Global Carbon Cycle" (PDF). University of New Hampshire. 2009. Retrieved 6 February 2016.
  6. Bird, M. (2015). "Test procedures for biochar in soil". In Lehmann, J.; Joseph, S. Biochar for Environmental Management (2 ed.). p. 679. ISBN 978-0-415-70415-1.
  7. Skjemstad, Jan O. (2002). "Charcoal carbon in U.S. agricultural soils". Soil Science Society of America Journal. 66 (4): 1249–1255. doi:10.2136/sssaj2002.1249.
  8. Schmidt, M.W.I.; Skjemstad, J.O.; Czimczik, C.I.; Glaser, B.; Prentice, K.M.; Gelinas, Y.; Kuhlbusch, T.A.J. (2001). "Comparative analysis of black C in soils" (PDF). Global Biogeochemical Cycles. 15: 163–168. doi:10.1029/2000GB001284.
  9. Mao, J.-D.; Johnson, R. L.; Lehmann, J.; Olk, J.; Neeves, E. G.; Thompson, M. L.; Schmidt-Rohr, K. (2012). "Abundant and stable char residues in soils: implications for soil fertility and carbon sequestration". Environmental Science and Technology. 46: 9571–9576. doi:10.1021/es301107c.
  10. Mergel, A. (1998). "Role of plant root exudates in soil carbon and nitrogen transformation". In Box, Jr., J. Root Demographics and Their Efficiencies in Sustainable Agriculture, Grasslands and Forest Ecosystems. Proceedings of the 5th Symposium of the International Society of Root Research. 82. Madren Conference Center, Clemson University, Clemson, South Carolina, USA: Springer Netherlands. pp. 43–54. doi:10.1007/978-94-011-5270-9_3. ISBN 978-94-010-6218-3.
  11. Pearson JN and Jakobsen I. 1993. The relative contribution of hyphae and roots to phosphorus uptake by arbuscular mycorrhizal plants, measured by dual labeling with 32P and 33P. New Phytologist, 124: 489-494.
  12. Hobbie JE and Hobbie EA. 2006. 15N in symbiotic fungi and plants estimates nitrogen and carbon flux rates in arctic tundra. Ecology, 87: 816-822
  13. Ruddiman, William (2007). Plows, Plagues, and Petroleum: How Humans Took Control of Climate. Princeton, NJ: Princeton University Press. ISBN 978-0-691-14634-8.
  14. 1 2 Young, A.; Young, R. (2001). Soils in the Australian landscape. Melbourne: Oxford University Press. ISBN 978-0-19-551550-3.
  15. Charman, P.E.V.; Murphy, B.W. (2000). Soils, their properties and management (2nd edn ed.). Melbourne: Oxford University Press. ISBN 978-0-19-551762-0.
  16. IPCC. 2000. Land use, land-use change and forestry. IPCC Special Report. United Kingdom, Cambridge University Press.
  17. IPCC. 2003. Good practice guidance for land use, land-use change and forestry. Kanagawa, Japan, National Greenhouse Gas Inventories Programme.
  18. IPCC. 2006. Guidelines for national greenhouse gas inventories. Kanagawa, Japan, National Greenhouse Gas Inventories Programme.
  19. Pan Y., Birdsey R., Fang J., Houghton R., Kauppi P., Kurz W., Phillips O., Shvidenko A., et al. (2011). "A Large and Persistent Carbon Sink in the World's Forests". Science. 333 (6045): 1201609. doi:10.1126/science.1201609.
  20. FAO. 2012. "Soil carbon monitoring using surveys and modelling: General description and application in the United Republic of Tanzania". FAO Forestry Paper 168 Rome. Available at: http://www.fao.org/docrep/015/i2793e/i2793e00.htm
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