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17 - The Use of Stable Isotopes in Understanding the Impact of Biochar on the Nitrogen Cycle

from Part IV - Biochar Application as a Soil Amendment

Published online by Cambridge University Press:  01 December 2016

By
Rebecca Hood-Nowotny
Edited by
Viktor J. Bruckman ,
Esin Apaydın Varol ,
Bașak B. Uzun  and
Jay Liu
Viktor J. Bruckman
Affiliation:
Austrian Academy of Sciences
Esin Apaydın Varol
Affiliation:
Anadolu University, Turkey
Bașak B. Uzun
Affiliation:
Anadolu University, Turkey
Jay Liu
Affiliation:
Pukyong National University, South Korea
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Summary

Abstract

The practice of applying biochar to soil could increase crop production and sequester carbon, whilst tightening leaky nitrogen cycles. Biochar has been shown to improve soil properties and even reduce greenhouse gas emissions, however the underlying mechanisms that lead to yield increases and GHG mitigation still elude us. Recent and ongoing studies have demonstrated that detailed analysis of the inherent biogeochemical processes using stable isotope techniques can unravel the complex soil–plant interactions and begin to tease out the multifaceted impacts of biochar on soil processes and plant growth. Here we present a range of nitrogen isotope techniques that could be, or have been, used to understand the changes in dominant processes in the nitrogen cycle following biochar addition.

Type
Chapter
Information
Biochar
A Regional Supply Chain Approach in View of Climate Change Mitigation
 , pp. 351 - 367
Publisher: Cambridge University Press
Print publication year: 2016

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References

Arah, J. R. M. (1997). Apportioning nitrous oxide fluxes between nitrification and denitrification using gas-phase mass spectrometry. Soil Biology and Biochemistry, 29, pp. 1295–1299.CrossRefGoogle Scholar
Arbenz, M., Willer, H., Lernoud, J., Huber, B. and Amarjit, S. (2015). The World of Organic Agriculture – Statistics and Emerging Trends (Session at the BioFach Congress 2015, Nuremberg, Germany, 11–15.2.2015).Google Scholar
Baggs, E. M. and Philippot, L. (2010). Microbial terrestrial pathways to nitrous oxide. In: Smith, K. (ed.) Nitrous Oxide and Climate Change. Oxford: Earthscan, pp. 4–35.Google Scholar
Baldock, J. and Skjemstad, J. (2000). Role of the soil matrix and minerals in protecting natural organic materials against biological attack. Organic Geochemistry, 31, pp. 697–710.CrossRefGoogle Scholar
Barraclough, D. (1991). The use of mean pool abundances to interpret 15N tracer experiments. Plant and Soil, 131, pp. 89–96.CrossRefGoogle Scholar
Barraclough, D. (1997). The direct route or MIT route for nitrogen immobilization: a 15N ‘mirror image’ study with leucine and glycine, Soil Biology and Biochemistry, 29, pp. 101–108.CrossRefGoogle Scholar
Bateman, E. J. and Baggs, E. M. (2005). Contributions of nitrification and denitrification to N2O emissions from soils at different water-filled pore space. Biology and Fertility of Soils, 41, pp. 379–388.CrossRefGoogle Scholar
Biederman, L. A. and Harpole, W. S. (2013). Biochar and its effects on plant productivity and nutrient cycling: a meta-analysis. GCB Bioenergy, 5, pp. 202–214.CrossRefGoogle Scholar
Birch, H. F. (1958). The effect of soil drying on humus decomposition and nitrogen availability. Plant and Soil, 10, pp. 9–31.CrossRefGoogle Scholar
Bowatte, S., Newton, P. C. D., Takahashi, R. et al. (2010). High frequency of virus-infected bacterial cells in a sheep grazed pasture soil in New Zealand. Soil Biology and Biochemistry, 42, pp. 708–712.CrossRefGoogle Scholar
Brennan, M. D., Cheong, R. and Levchenko, A. (2012). Systems biology. How information theory handles cell signaling and uncertainty. Science, 338, pp. 334–335.CrossRefGoogle ScholarPubMed
Bruun, E. W., Petersen, C., Strobel, B. W. et al. (2012). Nitrogen and carbon leaching in repacked sandy soil with added fine particulate biochar. Soil Science Society of America Journal, 76, pp. 1142–1148.CrossRefGoogle Scholar
Butterbach-Bahl, K., Baggs, E. M., Dannemann, M. et al. (2013). Nitrous oxide emissions from soils: how well do we understand the processes and their controls? Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences, 368, No.20130122.Google ScholarPubMed
Butterbach-Bahl, K., Willibald, G. and Papen, H. (2002). Soil core method for direct simultaneous determination of N2 and N2O emissions from forest soils. Plant and Soil, 240, pp. 105–116.CrossRefGoogle Scholar
Cayuela, M. L., Sánchez-Monedero, M. A., Roig, A. et al. (2013). Biochar and denitrification in soils: when, how much and why does biochar reduce N₂O emissions? Scientific Reports, 3, No.1732.CrossRefGoogle ScholarPubMed
Cayuela, M. L., van Zwieten, L., Singh, B. P. et al. (2014). Biochar’s role in mitigating soil nitrous oxide emissions: a review and meta-analysis. Agriculture, Ecosystems & Environment, 191, pp. 5–16.CrossRefGoogle Scholar
Cayuela, M. L., Jeffery, S. and van Zwieten, L. (2015). The molar H: Corg ratio of biochar is a key factor in mitigating N2O emissions from soil. Agriculture, Ecosystems & Environment, 202, pp. 135–138.CrossRefGoogle Scholar
Chen, Y., Shinogi, Y. and Taira, M. (2010). Influence of biochar use on sugarcane growth, soil parameters, and groundwater quality. Australian Journal of Soil Research, 48, pp. 526–530.CrossRefGoogle Scholar
Cheng, C., Lehmann, J. and Thies, J., 2006. Oxidation of black carbon by biotic and abiotic processes. Organic Geochemistry, 37, pp. 1477–1488.CrossRefGoogle Scholar
Cheng, Y., Cai, Z.-C., Chang, S. X. et al. (2012). Wheat straw and its biochar have contrasting effects on inorganic N retention and N2O production in a cultivated Black Chernozem. Biology and Fertility of Soils, 48, pp. 941–946.CrossRefGoogle Scholar
Christensen, T. and Jonasson, S. (1999). On the potential CO2 release from tundra soils in a changing climate. Applied Soil Ecology, 11, pp. 127–134.CrossRefGoogle Scholar
Cleveland, C. C., Townsend, A. R., Schimel, D. S. et al. (1999). Global patterns of terrestrial biological nitrogen (N2) fixation in natural ecosystems. Global Biogeochemical Cycles, 13, pp. 623–645.CrossRefGoogle Scholar
Clough, T., Condron, L. M., Kammann, C. et al. (2013). A review of biochar and soil nitrogen dynamics. Agronomy, 3, pp. 275–293.CrossRefGoogle Scholar
Clough, T. J. and Condron, L. M. (2010). Biochar and the nitrogen cycle: introduction. Journal of Environment Quality, 39, pp. 1218–1223.CrossRefGoogle ScholarPubMed
Coleman, D. C. (1994). The microbial loop concept as used in terrestrial soil ecology studies. Microbial Ecology, 28, pp. 245–250.CrossRefGoogle ScholarPubMed
Dempster, D. N., Jones, D. L. and Murphy, D. V. (2012). Clay and biochar amendments decreased inorganic but not dissolved organic nitrogen leaching in soil. Soil Research, 50, pp. 216–221.CrossRefGoogle Scholar
Ducey, T. F., Ippolito, J. A., Cantrell, K. B. et al. (2013). Addition of activated switchgrass biochar to an aridic subsoil increases microbial nitrogen cycling gene abundances. Applied Soil Ecology, 65, pp. 65–72.CrossRefGoogle Scholar
Fanzo, J., Remans, R. and Sanchez, P. (2011). The role of chemistry in addressing hunger and food security. In: Garcia-Martinez, J. and Serrano-Torregrosa, E. (eds.) The Chemical Element: Chemistry’s Contribution to our Global Future. London: Wiley, pp. 71–97.CrossRefGoogle Scholar
Fomsgaard, S. (2006). Organic Agriculture Movement at a Crossroad – a Comparative Study of Denmark and Japan. Working Paper OASE. Aalborg, Denmark: Aalborg University, Department of Economics Politics and Public Administratration.Google Scholar
Fürnkranz, M., Wanek, W., Richter, A. et al. (2008). Nitrogen fixation by phyllosphere bacteria associated with higher plants and their colonizing epiphytes of a tropical lowland rainforest of Costa Rica. The ISME Journal, 2, pp. 561–570.CrossRefGoogle ScholarPubMed
Galloway, J. N., Townsend, A. R., Erisman, J. W. et al. (2008). Transformation of the nitrogen cycle: recent trends, questions, and potential solutions. Science, 320, pp. 889–892.CrossRefGoogle ScholarPubMed
Ganry, F., Guiraud, G. and Dommergues, Y. (1978). Effect of straw incorporation on the yield and nitrogen balance in the sandy soil-pearl millet cropping system of Senegal. Plant and Soil, 50, pp. 647–662.CrossRefGoogle Scholar
Glaser, B., Haumaier, L., Guggenberger, G. et al. (2001). The ‘Terra Preta’ phenomenon: a model for sustainable agriculture in the humid tropics. Naturwissenschaften, 88, pp. 37–41.CrossRefGoogle Scholar
Güereña, D. Lehmann, J., Hanley, K. et al. (2012). Nitrogen dynamics following field application of biochar in a temperate North American maize-based production system. Plant and Soil, 365, pp. 239–254.CrossRefGoogle Scholar
Han, G. M., Meng, J., Zhang, W. M. et al. (2013). Effect of biochar on microorganisms quantity and soil physicochemical property in rhizosphere of spinach (Spinacia oleracea L.). Applied Mechanics and Materials, 295–298, pp. 210–219.CrossRefGoogle Scholar
Hart, S. C., Stark, J. M., Davidson, E. A. et al. (1994). Methods of soil analysis: part 2 – microbiological and biochemical properties. In: Bottomley, P. S., Angle, J. S. and Weaver, R. W. (eds.) Methods of Soil Analysis: Part 2 – Microbiological and Biochemical Properties. SSSA Book Series. Washington, DC: Soil Science Society of America, pp. 985–1018.Google Scholar
Harter, J., Krause, H.-M., Schuettler, S. et al. (2014). Linking N2O emissions from biochar-amended soil to the structure and function of the N-cycling microbial community. The ISME Journal, 8, pp. 660–674.CrossRefGoogle Scholar
Hood, R., Bautista, E. and Heiling, M. (2003). Gross mineralization and plant N uptake from animal manures under non-N limiting conditions, measured using 15N isotope dilution techniques. Phytochemistry Reviews, 2, pp. 113–119.CrossRefGoogle Scholar
Hood-Nowotny, R., Umana, N. H.-N., Inselbacher, E. et al. (2010). Alternative methods for measuring inorganic, organic, and total dissolved nitrogen in soil. Soil Science Society of America Journal, 74, pp. 1018–1027.CrossRefGoogle Scholar
Hu, H.-W., Chen, D. and He, J.-Z. (2015). Microbial regulation of terrestrial nitrous oxide formation: understanding the biological pathways for prediction of emission rates. FEMS Microbiology Reviews, 39, pp. 729–749.CrossRefGoogle ScholarPubMed
Inselsbacher, E., Wanek, W., Strauss, J. et al. (2013). A novel 15N tracer model reveals: plant nitrate uptake governs nitrogen transformation rates in agricultural soils. Soil Biology and Biochemistry, 57, pp. 301–310.CrossRefGoogle Scholar
Jackson, L. E., Burger, M. and Cavagnaro, T. R. (2008). Roots, nitrogen transformations, and ecosystem services. Annual Review of Plant Biology, 59, pp. 341–363.CrossRefGoogle ScholarPubMed
Jeffery, S., Abalos, D., Spokas, K. A. et al. (2015). Biochar effects on crop yield. In: Lehmann, J. and Joseph, S. (eds.) Biochar for Environmental Management: Science, Technology and Implementation. London: Earthscan, Routledge, pp. 301–325.Google Scholar
Jones, D. L., Rosuk, J., Edwards-Jones, G. et al. (2011). Biochar-mediated changes in soil quality and plant growth in a three year field trial. Soil Biology and Biochemistry, 45, pp. 113–124.CrossRefGoogle Scholar
Laird, D. and Rogovska, N. (2015). Biochar effects on nutrient leaching. In: Lehmann, J. and Joseph, S. (eds.) Biochar for Environmental Management: Science, Technology and Implementation. London: Earthscan, Routledge, pp. 521–542.Google Scholar
Laughlin, R. J., Stevens, R. J. and Müller, C. (2008). Evidence that fungi can oxidize NH4+ to NO3− in a grassland soil. European Journal of Soil Science, 59, pp. 285–291.CrossRefGoogle Scholar
Lehmann, J. (2007). A handful of carbon. Nature, 447, pp. 10–11.CrossRefGoogle ScholarPubMed
Lehmann, J. and Joseph, S. (eds.) (2015). Biochar for Environmental Management: Science, Technology and Implementation, London: Earthscan, Routledge.CrossRefGoogle Scholar
Li, M., Zhen, A. H., Ning, L. et al. (2012). Effects of biochar application on wheat growth and nitrogen balance. Xinjiang Agricultural Sciences, 49, pp. 589–594.Google Scholar
Malghani, S., Gleixner, G. and Trumbore, S. (2013). Chars produced by slow pyrolysis and hydrothermal carbonization vary in carbon sequestration potential and greenhouse gases emissions. Soil Biology and Biochemistry, 62, pp. 137–146.CrossRefGoogle Scholar
McNeill, A., Hood, R. and Wood, M. (1994). Direct measurement of nitrogen fixation by Trifolium repens L. and Alnus glutinosa L. using 15N2. Journal of Experimental Botany, 45, pp.749–755.CrossRefGoogle Scholar
Monaghan, R. (1995). Errors in estimates of gross rates of nitrogen mineralization due to non-uniform distributions of 15N label, Soil Biology and Biochemistry, 27, pp. 855–859.CrossRefGoogle Scholar
Nelissen, V., Rüttig, T., Huygens, D. et al. (2012). Maize biochars accelerate short-term soil nitrogen dynamics in a loamy sand soil. Soil Biology and Biochemistry, 55, pp. 20–27.CrossRefGoogle Scholar
Pietikainen, J., Kiikkila, O. and Fritze, H. (2000). Charcoal as a habitat for microbes and its effect on the microbial community of the underlying humus. Oikos, 89, pp. 231–242.CrossRefGoogle Scholar
Prommer, J., Wanek, W., Hofhansl, F. et al. (2014). Biochar decelerates soil organic nitrogen cycling but stimulates soil nitrification in a temperate arable field trial. PloS One, 9, No.e86388.CrossRefGoogle Scholar
Recous, S., Aita, C. and Mary, B. (1998). In situ changes in gross N transformations in bare soil after addition of straw. Soil Biology and Biochemistry, 31, pp. 119–133.CrossRefGoogle Scholar
Sánchez-García, M. (2014). Biochar increases soil N2O emissions produced by nitrification-mediated pathways. Frontiers in Environmental Science, 2, pp. 1–10.Google Scholar
Schimel, J. P. and Bennett, J. (2004). Nitrogen mineralization: challenges of a changing paradigm. Ecology, 85, pp. 591–602.CrossRefGoogle Scholar
Schimel, J. P. and Weintraub, M. N. (2003). The implications of exoenzyme activity on microbial carbon and nitrogen limitation in soil: a theoretical model. Soil Biology and Biochemistry, 35, pp. 549–563.CrossRefGoogle Scholar
Schmidt, M. W. I. and Noack, A. G. (2000). Black carbon in soils and sediments: analysis, distribution, implications, and current challenges. Global Biogeochemical Cycles, 14, pp. 777–793.CrossRefGoogle Scholar
Singh, B. P. and Cowie, A. L. (2014). Long-term influence of biochar on native organic carbon mineralisation in a low-carbon clayey soil. Scientific Reports, 4, No.3687.CrossRefGoogle Scholar
Six, J. and Jastrow, J. (2002). Organic matter turnover. In: Encyclopedia of Soil Science. New York: Marcel Dekker, pp. 936–942.Google Scholar
Spokas, K. A., Koskinen, W. C., Baker, J. M. and Reicosky, D. C. (2009). Impacts of woodchip biochar additions on greenhouse gas production and sorption/degradation of two herbicides in a Minnesota soil. Chemosphere, 77, pp. 574–581.CrossRefGoogle Scholar
Spott, O. and Stange, C. F. (2007). A new mathematical approach for calculating the contribution of anammox, denitrification and atmosphere to an N2 mixture based on a 15N tracer technique. Rapid Communications in Mass Spectrometry, 2, pp. 2398–2406.CrossRefGoogle Scholar
Steffen, W., Richardson, K., Rockström, J. et al. (2015). Planetary boundaries: guiding human development on a changing planet. Science, 347, doi: 10.1126/science.1259855.CrossRefGoogle ScholarPubMed
Steiner, C., Teixeira, W. G., Lehmann, J. et al. (2007). Long term effects of manure, charcoal and mineral fertilization on crop production and fertility on a highly weathered Central Amazonian upland soil. Plant and Soil, 291, pp. 275–290.CrossRefGoogle Scholar
Steiner, C., Glaser, B., Teixeira, W. G. et al. (2008). Nitrogen retention and plant uptake on a highly weathered central Amazonian Ferralsol amended with compost and charcoal. Journal of Plant Nutrition and Soil Science, 171, pp. 893–899.CrossRefGoogle Scholar
Stevens, R. J., Laughlin, R. J., Burns, L. C. et al. (1997). Measuring the contributions of nitrification and denitrification to the flux of nitrous oxide from soil. Soil Biology and Biochemistry, 29, pp. 139–151.CrossRefGoogle Scholar
Sutka, R. and Ostrom, N. (2006). Distinguishing nitrous oxide production from nitrification and denitrification on the basis of isotopomer abundances. Applied and Environmental Microbiology, 72, pp. 638–644.CrossRefGoogle ScholarPubMed
Sutton, M. A., Reis, S., Billen, G. et al. (2012). Preface: ‘Nitrogen and global change’. Biogeosciences, 9, pp. 1691–1693.CrossRefGoogle Scholar
Taghizadeh-Toosi, A., Clough, T. J., Sherlock, R. R. et al. (2011a). A wood based low-temperature biochar captures NH3-N generated from ruminant urine-N, retaining its bioavailability. Plant and Soil, 353, pp. 73–84.CrossRefGoogle Scholar
Taghizadeh-Toosi, A., Clough, T. J., Sherlock, R. R. et al. (2011b). Biochar adsorbed ammonia is bioavailable. Plant and Soil, 350, pp. 57–69.CrossRefGoogle Scholar
Tilman, D., Cassman, K. G., Matson, P. A. et al. (2002). Agricultural sustainability and intensive production practices. Nature, 418, pp. 671–677.CrossRefGoogle ScholarPubMed
Trumbore, S. (2000). Age of soil organic matter and soil respiration: radiocarbon constraints on belowground C dynamics. Ecological Applications, 10, pp. 399–411.CrossRefGoogle Scholar
Vaccari, F., Baronti, S., Lugato, E. et al. (2011). Biochar as a strategy to sequester carbon and increase yield in durum wheat. European Journal of Agronomy, 34, pp. 231–238.CrossRefGoogle Scholar
Van Zwieten, L., Kammann, C., Cayuela, M. L. et al. (2015). Biochar effects on nitrous oxide and methane emissions from soil. In: Lehmann, J. and Joseph, S. (eds.) Biochar for Environmental Management: Science, Technology and Implementation. London: Earthscan, Routledge, pp. 489–520.Google Scholar
Ventura, M. Sorrenti, G., Panzacchi, P. et al. (2012). Biochar reduces short-term nitrate leaching from a horizon in an apple orchard. Journal of Environmental Quality, 42, pp. 76–82.CrossRefGoogle Scholar
Wanek, W., Mooshammer, M., Blöchl, A. et al. (2010). Determination of gross rates of amino acid production and immobilization in decomposing leaf litter by a novel 15N isotope pool dilution technique. Soil Biology and Biochemistry, 42, pp. 1293–1302.CrossRefGoogle Scholar
Watkins, N. and Barraclough, D. (1996). Gross rates of N mineralization associated with the decomposition of plant residues. Soil Biology and Biochemistry, 28, pp. 169–175.CrossRefGoogle Scholar
Xiang, J., Liu, D., Yuan, J. et al. (2014). Effects of biochar on nitrous oxide and nitric oxide emissions from paddy field during the wheat growth season. Journal of Cleaner Production, 104, pp. 52–58.CrossRefGoogle Scholar

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