Biochar has become a popular soil amendment. However, its effect on soil microbial community is still unclear. In the present study, maize straw biochar was pyrolysed at 300°C, 450°C and 600°C, respectively, and then was added to agricultural soil at the ratio of 0.5%, 1% and 2%. Bacterial dynamics was analyzed in the pot experiments using denaturing gradient gel electrophoresis. The results indicated that the pyrolysis temperature has great impact on the elemental composition, pH and porous structures of biochar. Moreover, pyrolysis temperature was primary factor to drive the variation of bacterial community structure in biochar amended soil. In addition, the results suggested that biochar amendments on agricultural soil would decrease the bacterial diversity, and selectively promote growth of functional bacteria to become the dominant community, which could increase the bacterial community organization and improve the stability of bacteria to counteract effects of perturbation.
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ASTM D3838-05 (2017) Standard test method for pH of activated carbon. ASTM International, West Conshohocken. https://doi.org/10.1520/D3838-05R17
Bashir S, Shaaban M, Mehmood S, Zhu J, Fu QL, Hu HQ (2018) Efficiency of C3 and C4 plant derived-biochar for Cd mobility, nutrient cycling and microbial biomass in contaminated soil. Bull Environ Contam Toxicol 100:834–838. https://doi.org/10.1007/s00128-018-2332-6
Cernansky R (2015) State-of-the-art soil. Nature 517:258–260. https://doi.org/10.1038/517258a
Chen J, Liu X, Zheng J, Zhang B, Lu H, Chi Z, Pan G, Li L et al (2013) Biochar soil amendment increased bacterial but decreased fungal gene abundance with shifts in community structure in a slightly acid rice paddy from Southwest China. Appl Soil Ecol 71:33–44. https://doi.org/10.1016/j.apsoil.2013.05.003
Dai Z, Barberan A, Li Y, Brookes PC, Xu J (2017) Bacterial community composition associated with pyrogenic organic matter (biochar) varies with pyrolysis temperature and colonization environment. Msphere 2:e00085–e00017. https://doi.org/10.1128/mSphere.00085-17
Dempster DN, Gleeson DB, Solaiman ZM, Jones DL, Murphy DV (2012) Decreased soil microbial biomass and nitrogen mineralisation with Eucalyptus biochar addition to a coarse textured soil. Plant Soil 354:311–324. https://doi.org/10.1007/s11104-011-1067-5
Gul S, Whalen JK, Thomas BW, Sachdeva V, Deng HY (2015) Physico-chemical properties and microbial responses in biochar-amended soils: mechanisms and future directions. Agric Ecosyst Environ 206:46–59. https://doi.org/10.1016/j.agee.2015.03.015
Gundale MJ, DeLuca TH (2006) Temperature and source material influence ecological attributes of ponderosa pine and Douglas-fir charcoal. For Ecol Manag 231:86–93. https://doi.org/10.1016/j.foreco.2006.05.004
Imparato V, Hansen V, Santos SS, Nielsen TK, Giagnoni L, Hauggaard-Nielsen H, Johansen A, Renella G et al (2016) Gasification biochar has limited effects on functional and structural diversity of soil microbial communities in a temperate agroecosystem. Soil Biol Biochem 99:128–136. https://doi.org/10.1016/j.soilbio.2016.05.004
Khodadad CL, Zimmerman AR, Green SJ, Uthandi S, Foster JS (2011) Taxa-specific changes in soil microbial community composition induced by pyrogenic carbon amendments. Soil Biol Biochem 43:385–392. https://doi.org/10.1016/j.soilbio.2010.11.005
Lehmann J, Rillig MC, Thies J, Masiello CA, Hockaday WC, Crowley D (2011) Biochar effects on soil biota – a review. Soil Biol Biochem 43:1812–1836. https://doi.org/10.1016/j.soilbio.2011.04.022
Liu J, Yu Y, Cai Z, Bartlam M, Wang Y (2015) Comparison of ITS and 18S rDNA for estimating fungal diversity using PCR-DGGE. World J Microbiol Biotechnol 31:1387–1395. https://doi.org/10.1007/s11274-015-1890-6
Liu J, Ding Y, Ma L, Gaohttps://doi.org/ G, Wang Y (2017) Combination of biochar and immobilized bacteria in cypermethrin-contaminated soil remediation. Int Biodeterior Biodegrad 120:15–20. https://doi.org/10.1016/j.ibiod.2017.01.039
Liu J, Tu T, Gao G, Bartlam M, Wang Y (2019) Biogeography and diversity of freshwater bacteria on a river catchment scale. Microb Ecol 78:324–335. https://doi.org/10.1007/s00248-019-01323-9
Liu SJ, Liu YG, Tan XF, Zeng GM, Zhou YH, Liu SB, Yin ZH, Jiang LH et al (2018) The effect of several activated biochars on Cd immobilization and microbial community composition during in-situ remediation of heavy metal contaminated sediment. Chemosphere 208:655–664. https://doi.org/10.1016/j.chemosphere.2018.06.023
Marzorati M, Wittebolle L, Boon N, Daffonchio D, Verstraete W (2008) How to get more out of molecular fingerprints: practical tools for microbial ecology. Environ Microbiol 10:1571–1581. https://doi.org/10.1111/j.1462-2920.2008.01572.x
Muhammad N, Dai Z, Xiao K, Meng J, Brookes PC, Liu X, Wang H, Wu J et al (2014) Changes in microbial community structure due to biochars generated from different feedstocks and their relationships with soil chemical properties. Geoderma 226:270–278. https://doi.org/10.1016/j.geoderma.2014.01.023
Mukherjee A, Zimmerman AR, Harris W (2011) Surface chemistry variations among a series of laboratory-produced biochars. Geoderma 163:247–255. https://doi.org/10.1016/j.geoderma.2011.04.021
Nielsen UN, Ayres E, Wall DH, Bardgett RD (2011) Soil biodiversity and carbon cycling: a review and synthesis of studies examining diversity–function relationships. Eur J Soil Sci 62:105–116. https://doi.org/10.1111/j.1365-2389.2010.01314.x
Palansooriya KN, Wong JTF, Hashimoto Y, Huang L, Rinklebe J, Chang SX, Bolan N, Wang H et al (2019) Response of microbial communities to biochar-amended soils: a critical review. Biochar 1:3–22. https://doi.org/10.1007/s42773-019-00009-2
Prigogine I, Nicolis G, Babloyantz A (1974) Nonequilibrium problems in biological phenomena. Ann N Y Acad Sci 231:99–105. https://doi.org/10.1111/j.1749-6632.1974.tb20557.x
Read S, Marzorati M, Morais Guimarães B, Boon N (2011) Microbial resource management revisited: successful parameters and new concepts. Appl Microbiol Biotechnol 90:861–871. https://doi.org/10.1007/s00253-011-3223-5
Saito M, Marumoto T (2002) Inoculation with arbuscular mycorrhizal fungi: the status quo in Japan and the future prospects. Plant Soil 244:273–279. https://doi.org/10.1023/a:1020287900415
Samonin VV, Elikova EE (2004) A study of the adsorption of bacterial cells on porous materials. Microbiology 73:696–701. https://doi.org/10.1007/s11021-005-0011-1
Song D, Tang J, Xi X, Zhang S, Liang G, Zhou W, Wang X (2018) Responses of soil nutrients and microbial activities to additions of maize straw biochar and chemical fertilization in a calcareous soil. Eur J Soil Biol 84:1–10. https://doi.org/10.1016/j.ejsobi.2017.11.003
Song Y, Bian Y, Wang F, Xu M, Ni N, Yang X, Gu C, Jiang X (2017) Dynamic effects of biochar on the bacterial community structure in soil contaminated with polycyclic aromatic hydrocarbons. J Agric Food Chem 65:6789–6796. https://doi.org/10.1021/acs.jafc.7b02887
Van Zwieten L, Kimber S, Morris S, Chan KY, Downie A, Rust J, Joseph S, Cowie A (2010) Effects of biochar from slow pyrolysis of papermill waste on agronomic performance and soil fertility. Plant Soil 327:235–246. https://doi.org/10.1007/s11104-009-0050-x
Van Zwieten L, Kimber S, Morris S, Macdonald LM, Rust J, Petty S, Joseph S, Rose T (2019) Biochar improves diary pasture yields by alleviating P and K constraints with no influence on soil respiration or N2O emissions. Biochar 1:115–126. https://doi.org/10.1007/s42773-019-00005-6
Wei J, Tu C, Yuan G, Bi D, Wang H, Zhang L, Theng BKG (2019) Pyrolysis temperature-dependent changes in the characteristics of biochar-borne dissolved organic matter and its copper binding properties. Bull Environ Contam Toxicol 103:169–174. https://doi.org/10.1007/s00128-018-2392-7
Wittebolle L, Marzorati M, Clement L, Balloi A, Daffonchio D, Heylen K, De Vos P, Verstraete W et al (2009) Initial community evenness favours functionality under selective stress. Nature 458:623–626. https://doi.org/10.1038/nature07840
Yu L, Yuan Y, Tang J, Wang Y, Zhou S (2015) Biochar as an electron shuttle for reductive dechlorination of pentachlorophenol by Geobacter sulfurreducens. Sci Rep 5:16221. https://doi.org/10.1038/srep16221
Zhang D, Ding A (2019) Effects of passivating agents on the availability of Cd and Pb and microbial community function in a contaminated acidic soil. Bull Environ Contam Toxicol 103:98–105. https://doi.org/10.1007/s00128-019-02592-3
This work was supported by the National Key Basic Research Program of China [2015CB459000] and National Science Foundation of China .
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Liu, J., Ding, Y., Ji, Y. et al. Effect of Maize Straw Biochar on Bacterial Communities in Agricultural Soil. Bull Environ Contam Toxicol 104, 333–338 (2020). https://doi.org/10.1007/s00128-020-02793-1
- Agricultural soil
- Bacterial community
- Dissipative structures
- Pyrolysis temperature