An Introduction to Fire and Soil Carbon
Austin K. Dixon1, Kevin M. Robertson1, David R. Godwin2
1Tall Timbers Research Station
2University of Florida
Publication ID: Fact Sheet 2019-1 Published: 2019 Revised: 2026
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Importance of Soil Carbon
Historically, the interest in fire effects on soil carbon was focused on soil organic matter because of its importance to nutrient retention and overall soil health. Soil organic matter contains organic compounds that can be mineralized and released through decomposition into nutrients for plants. It also provides substrates that hold nutrients and slow down their leaching and loss from the plant root zone. Additionally, it influences soil hydrology, serving to retain moisture when wet and, in some cases, repel moisture when dry.
In recent years, the interest in soil carbon has shifted to the potential for sequestration and storage of carbon to mitigate the effects of climate change driven by emissions from fossil fuels. About 55% of the extra carbon dioxide (CO2) produced by humans has been re-absorbed by the ocean, plants, and the soil, which serve as sinks (repositories) of carbon fixed through photosynthesis by plants and green algae. Soil carbon originates from many sources, including death of root tissue, root exudates (chemicals exuded for defense against pathogens), soil microorganisms, and introduction of dead plant and animal material to the soil surface. In the southeastern U.S., soils contain at least three times more organic carbon than the atmosphere or terrestrial plants (Schmidt et al. 2011), making it an important sink for global carbon. Soil carbon is important because it is a more stable sink than carbon in vegetation, which is subject to sudden losses to wildfire, harvest for food or short-lived wood products, land clearing, slash or stubble burning, and herbivory, which release CO2 back into the atmosphere (Stainback and Alavalapati 2008). Even so, some carbon is continually re-emitted into the atmosphere through respiration by fungi and bacteria as they decompose organic matter as well as through combustion during fires.
Combustion by fire converts organic matter and living biomass primarily into carbon dioxide as well as other carbon-based compounds and minerals (Figure 1). However, between periodic fires, carbon dioxide is re-sequestered into the re-growing vegetation through photosynthesis, typically resulting in no net change in atmospheric CO2 if the ecosystem is not greatly altered by fire exclusion, unnaturally severe fire, or other land use changes. In the case of mineral soils in the South, individual fires are rarely severe enough to have a strong direct effect on soil carbon. Rather, it is the effect of fire regime, which influences ecosystem structure and function over time, that has the most important long-term effects on soil carbon sequestration or loss.
Duration of Soil Carbon Storage
Different components of soil carbon move through the carbon cycle at different rates. These carbon components have been classified as transient, temporary, and persistent. Transient carbon, including starches and cellulose, decomposes quickly, resulting in turnover of organic carbon into CO2 on the time scale of around 2-8 weeks, depending on the chemistry of the organic matter and decomposers present in the soil. Temporary carbon, such as dead roots and fungal hyphae, remains in soils between 2-12 months. Persistent carbon produced by heating, including pyrogenic carbon or black carbon, can remain for a year to thousands of years. This black carbon has been seen to enhance cation exchange capacity in some southeastern forest soils (Liang et al. 2008). The amount of black carbon found in the soil varies greatly among soils studied but is typically less than a third of the total carbon (Masiello 2004, Hsieh and Bugna 2008).
Direct Effects of Fire on Soil Carbon
Fire can directly influence soil carbon in several ways. First, soil organic matter and living biomass (e.g. duff, roots, soil organisms) can be consumed through combustion (Dixon and Robertson 2018). Heat from smoldering combustion of organic soil may combust some of the organic matter in the underlying mineral soil. The destruction of organic matter and microbial communities can indirectly affect soil carbon by slowing down decomposition rates of remaining organic material, reducing nutrient availability, and reducing plant productivity through damage to mycorrhizal networks (Cerligione et al. 1988).
Fire Effects on Soil Carbon in Southern U.S. Communities
In southeastern U.S. pine communities, the effects of frequent burning (1-3 year fire return intervals mimicking historical conditions) are typically slight and often positive with regard to total soil carbon (Heyward and Barnette 1934, Greene 1935, Wells 1971, McKee 1982, Godwin et al. 2017) (see Figure 2). Current evidence suggests stable or increased levels of soil carbon under frequent burning are a result of decreased rates of turnover (decomposition) of soil organic matter in the soil, which tips the balance toward soil carbon accumulation instead of loss. Slower turnover rates in burned versus unburned old-field pinelands has been indicated by isotope analysis (Hsieh et al. unpublished data) and suggested by lower CO2 emissions from soils of burned areas (Godwin et al. 2017). Higher levels of soil C in burned versus unburned areas also have been found in pine communities outside of the region, including southwestern U.S. ponderosa pine woodland (Neary 2003), New Jersey pitch pine barrens (Burns 1952), and maritime pine (P. pinaster) woodlands of the Iberian peninsula (Mayor et al. 2016). The mechanisms by which periodic fire reduces decomposition rates are not yet known, but they could include one or more of the following: direct effects on microbes, effects on plant species composition, and increased stability of organic matter introduced into the soil.
Fire Effects on Microbes
Fire can have differential impacts on soil microbial activity which can influence the decomposition of soil organic matter. Fire can negatively impact soil microbial activity through heating and it can also positively impact soil microbial activity through the release of previously unavailable minerals and favorable changes to the microbe environment such as increased temperature or moisture. In the case of mineral soils, microbe death is usually associated with combustion of coarse fuels releasing heat over a long period of time, which can heat and even sterilize the soil. In the case of organic soils, microbes can be killed directly through soil consumption in addition to heating. In either case, decomposition can be reduced during the recovery period (Godwin et al. 2017). Fire also changes soil chemistry, including nutrients, which can alter the activity of soil microbes. Soil bulk density often increases with the occurrence of fire, attributed to char and ash filling the micro-pore space, which decreases oxygen availability and microbial activity (Neary et al. 1999).
Fire typically releases a pulse of mineral nutrients (e.g., Ca, P, Mg, K) which might be expected to increase microbial activity, but N is less predictable (Christensen 1977) and may decrease following fires. Preliminary research in longleaf pine communities also suggests that fire and time since fire influences the composition of soil fungi and bacteria (Sikes et al. unpublished data). Fungal composition and environmental conditions can influence microbial carbon use efficiency, which describes how much biomass digested by microbes is converted to microbial biomass and exudates as opposed to being released as CO2 (Manzoni et al. 2012).
Changes in Plant Species Composition
Fire regime has strong effects on species composition and associated soil carbon dynamics. Frequent fire typically promotes dominance by C4 grasses, forbs, and fire-tolerant trees (often conifers) and prevents dominance by broad-leaved woody plants and vines (Bond and Keeley 2005). While grasslands average 20% higher soil respiration than forest stands on similar soils (Raich and Tufekcioglu 2000), C4 grasses typically decompose more slowly than C3 plants (Martin et al. 1990), which may contribute to carbon accumulation. Additionally, conifer forests have 10% lower soil respiration rates than broad-leaved forests of the same soil type (Raich and Tufekcioglu 2000; Yuste et al. 2005). Grasses have abundant fine roots and higher rates of root turnover, a major contributor to soil carbon. Fine roots (2 mm or less in diameter), which account for more than 30% of global total net primary production (Jackson et al 1997), are short-lived, replacing themselves up to three times per year (West et al. 2004), so they contribute a great deal of organic matter to the soil.
Fine roots also influence soil carbon through their bacterial and fungal symbionts. While microbial activity generally promotes decomposition (Schmidt et al 2011), ectomycorrhizal fungi may slow the decomposition of roots (Langley et al 2006) and lengthen the period of organic matter retention. Mineralized soil carbon was found to be significantly higher under C4 bunchgrasses than adjacent locations in southeastern pine savannas, suggesting both additions from root turnover and increased microbial activity (West and Donavan 2004). It follows that in southern pinelands, soil carbon sequestration likely depends on management that promotes grasses and other herbs, specifically frequent fire and timber management that maintains an open canopy. Some research has found replacement of grasslands with dense pine forest results in decreased soil carbon. In longleaf pine dominated communities, known for the dominance of bunch grasses in surface layer vegetation, fine roots likely play an important role in mediating carbon fluxes (Guo et al. 2004).
Changes to Carbon Stability
Fire typically changes some biomass into chemically more stable forms. One explanation for the accumulation of soil carbon in frequently burned southern pine communities is that the most flammable fuels are also the most susceptible to decomposition, such that inputs to the soil from fuel not consumed by fire are less palatable to microbes (Wells 1971). Also, fire converts part of the fuel into char, also known as black carbon or elemental carbon, formed from the heating and gasification of volatile chemicals leaving behind almost pure carbon. Molecular composition and stability of black carbon resulting from fire can vary widely depending on the fuel source, fire intensity, and specific fire conditions (Lehmann et al. 2006, Nguyen et al. 2010, Coates et al. 2017), but in general they are quite stable and tend to accumulate in soils. In southeastern U.S. pine communities, char is formed from fallen trees and stumps, branches and twigs, pine cones, and pine needles. However, comparison of frequently burned (1-2 year interval) and a 50-year unburned site that was previously frequently burned showed no measurable differences in amounts of char, suggesting that char accumulation is very slow (Hsieh and Robertson, unpublished data).
Relevance to Management
Although a certain amount of “gray literature” in the past few decades has suggested that fire reduces soil carbon in southeastern U.S. pinelands, scientific evidence suggests that application of frequent prescribed fire regimes will not significantly decrease soil carbon and may increase it. Although the mechanisms of soil carbon retention and accumulation in frequently burned pinelands are not precisely known, it seems advisable to burn frequently enough to prevent conversion from grass-dominated to woody-dominated communities and to manage timber to allow sufficient light penetration to maintain a continuous herbaceous community. Soil disturbance should also be minimized as soil aeration by disking greatly increases rates of soil organic matter decomposition (Wood and Edwards 1992) and was found to decrease soil C by 50% in a longleaf pine savanna (Robertson unpublished data). Burn piles of heavy slash, which likely volatize most of the near-surface soil carbon, should be located in previously disturbed sites, such as past burn pile locations or disked fields, that have initially low soil carbon. Soil carbon sequestration is likely to become an increasingly important goal of land management as markets for carbon credits expand (Dwivedi et al. 2009, McKinley et al. 2011).
References
- Berthrong, S. T., E. G. Jobbagy, and R. B. Jackson. (2009) A global meta-analysis of soil exchangeable cations, pH, carbon, and nitrogen with afforestation. Ecological Applications 19:2228–2241.
- Bond WJ, Keeley JE (2005) Fire as a global ‘herbivore’: the ecology and evolution of flammable ecosystems. TRENDS in Ecology and Evolution 20:387-394.
- Burns, P. Y. 1952. Effect of fire on forest soils in the Pine Barren region of New Jersey. Yale School of Forestry Bulletin No. 57. Yale University, New Haven, CT. 50 pp.
- Cerligione LJ, Liberta AE, Anderson RC (1988) Effects of soil moisture and soil sterilization on vesicular-arbuscular mycorrhizal colonization and growth of little bluestem (Schizachyrium scoparium). Canadian Journal of Botany 66:757-761.
- Christensen NL (1977) Fire and soil-plant nutrient relations in a pine-wiregrass savanna on the coastal plain of North Carolina. Oecologia 31:27-44.
- Coates TA, Chow AT, Hagan DL, Wang GG, Bridges WC, Dozier JH (2017) Frequent prescribed burning as a long-term practice in longleaf pine forests does not affect detrital chemical composition. Journal of Environmental Quality 46:1020-1027.
- Dxon, AK, Robertson, KM. 2018 Reintroducing Fire Into Long-Unburned Pine Stands: The Duff Problem. Southern Fire Exchange Fact Sheet 2018-4
- Dwivedi, P., J.R.R. Alavalapati, A. Susaeta, and A. Stainback. 2009. Impact of carbon value on the profitability of slash pine plantations in the southern United States: an integrated life cycle and Faustmann analysis. Canadian Journal of Forest Research 39:990-1000.
- Godwin DR, Kobziar LN, Robertson KM (2017) Effects of fire frequency and soil temperature on soil CO2 efflux rates in old-field pine-grassland forests. Forests 8:274.
- Guo DL, Mitchell RJ, Hendricks JJ (2004) Fine root branch orders respond differentially to carbon source-sink manipulations in a longleaf pine forest. Oecologia 140:450-457.
- Greene, S. W. 1935. Effect of annual grass fires on organic matter and other constituents of virgin longleaf pine soils. Journal of Agricultural Research 50:809-822.
- Heyward, F., and R.M. Barnette. 1934. Effect of frequent fires on chemical composition of forest soils in teh longleaf pine region. University of Florida Agricultural Experiment Station Technical Bulletin 265. Gainesville, Florida. 39 pp.
- Jackson RB, Mooney HA, Schulze ED (1997) A global budget for fine root biomass, surface area, and nutrient contents. Proceedings of the National Academy of Science 94:7362-7366.
- Langley JA, Chapman SK, Hungate BA (2006) Ectomycorrhizal colonization slows root decomposition: the post-mortem fungal legacy. Ecology Letters 9:955-959.
- Lehmann J, Gaunt J, Rondon M (2006) Bio-char sequestration in terrestrial ecosystems – A review. Mitigation and Adaptation Strategies for Global Change 11:403-427.
- Liang B, Lehmann J, Solomon D, Kinyangi J, Grossman J, O’Neill B, Skjemstad JO, Thies J, Luizao FJ, Petersen J, Neves EG (2006) Black carbon increase cation exchange capacity in soils. Soil Science Society of America Journal 70:1719-1730.
- Manzoni, S., P. Taylor, A. Richter, A. Porportato, and G.I. Agren. 2012. Environmental and stoichiometric controls on microbial carbon-use efficiency in soils. New Phytologist 196:79-91.
- Martin, A., A. Mariotti, J. Balesdent, P. Lavelle, and R. Vuattoux. 1990. Estimate of organic matter turnover rate in a savanna soil by 13C natural abundance measurements. Soil Biology and Biochemistry 22:517-523.
- Mayor, A. G., A. Valdecantos, V. R. Vellejo, J. J. Keizer, J. Bloem, J. Baeza, O. Gonzalez-Pelayo, A. I. Machado and P. C. de Ruiter (2016) Fire-induced woodland to shrubland transitions in Southern Europe may promote shifts in soil fertility. Science of the Total Environment 573:1232-1241.
- McKee, W. H. (1982) Changes in soil fertility following prescribed burning on Coastal Plain pine sites. Research Paper SE-234. USDA Forest Service Southeastern Experimental Forest Research Station, Charleston, South Carolina, 23 pg.
- McKinley, D.C., M.G. Ryan, R.A. Birdsey, C.P. Giardina, M.E. Harmon, L.S. Heath, R.A. Houghton, R.B. Jackson, J.F. Morrison, B.C. Murray, D.E. Pataki, and K.E. Skog. (2011) A synthesis of current knowledge on forests and carbon storage in the United States. Ecological Applications 21:1902-1924.
- Neary DG, Klopatek CC, DeBano LF, Ffolliott PF (1999) Fire effects on belowground sustainability: a review and synthesis. Forest Ecology and Management 122:51-71.
- Nguyen BT, Lehmann J, Hockaday WC, Joseph S, Masiello CA (2010) Temperature sensitivity of black carbon decomposition and oxidation. Environmental Science and Technology 44:3324-3331.
- Raich JW, Tufekcioglu A (2000) Vegetation and soil respiration: correlations and controls. Biogeochemistry 48:71-90.
- Schmidt MW, Torn MS, Abiven S, Dittmar T, Guggenberger G, Janssens IA, Kleber M, Kogel-Knabner I, Lehmann J, Manning DAC, Nannipieri P, Rasse DP, Weiner S, Trumbore SE (2011) Persistence of soil organic matter as an ecosystem property. Nature 478(7367):49-56.
- Stainback, G.A. and J.R.R.A. Alavalapati. 2004. Modeling catastrophic risk in economic analysis of forest carbon sequestration. Natural Resource Modeling 17:213-317.
- Wells, C. G. 1971. Effects of prescribed burning on soil chemical properties and nutrient availability. Pages 86-99 in Prescribed Burning Symposium Proceedings. USDA Forest Service Southeastern Forest Experiment Station, Charleston, SC. Yuste JC, Nagy M, Janssens IA, Carrara A, Ceulemans R (2005) Soil respiration in a mixed temperate forest and its contribution to total ecosystem respiration. Tree Physiology 25:609-619.
- West JB, Espeleta JF, Donovan LA (2004) Fine root production and turnover across a complex edaphic gradient of a Pinus palustris – Aristida stricta savanna ecosystem. Forest Ecology and Management 189:397-406.
- Yuste JC, Nagy M, Janssens IA, Carrara A, Ceulemans R (2005) Soil respiration in a mixed temperate forest and its contribution to total ecosystem respiration. Tree Physiology 25:609-619.