Abstract
Spent mushroom substrate (SMS) is a kind of agricultural waste currently used as amendment, however, its remediation efficacy on heavy metal-contaminated soil has not been comprehensively evaluated. In this study, the effects of SMS and its compost (CSMS) on soil environment (including lead availability, physicochemical properties, nutrient content, enzyme activity, bacterial community) and plant growth (including germination, photosynthesis, and biomass) in lead-contaminated soil were investigated. Independent germination test and pot experiments of water spinach were carried out under 600 mg/kg lead contamination and 5% amendment dosage. The results showed that SMS increased the germination rate by 45.1% and CSMS decreased it by 60.9%. Both amendments enhanced the photosynthesis and increased the fresh weight of water spinach by more than 12.6% in polluted soil, but SMS had a negative effect on photosynthesis and decreased the fresh weight in unpolluted soil. The SMS and CSMS reduced soil lead availability and thus decreased the lead content of water spinach by more than 6.1%. SMS increased soil pH, while CSMS decreased it. CSMS increased soil conductivity, organic carbon, and available N more than SMS. Both amendments consistently and positively impacted on soil enzymes and bacteria. In conclusion, composting is beneficial to increase the available N of SMS, which prevents SMS from competing with plants for N during mineralization. However, CSMS should not be directly used in the sowing period, because its alkalinity and high salt content may inhibit seed germination.
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The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
References
Kumar S, Prasad S, Yadav KK, Shrivastava M, Gupta N, Nagar S, Bach QV, Kamyab H, Khan SA, Yadav S, Malav LC (2019) Hazardous heavy metals contamination of vegetables and food chain: role of sustainable remediation approaches-A review. Environ Res 179:108792. https://doi.org/10.1016/j.envres.2019.108792
Zhang HW, Zhang F, Song J, Tan ML, Kung HT, Johnson VC (2021) Pollutant source, ecological and human health risks assessment of heavy metals in soils from coal mining areas in Xinjiang, China. Environ Res 202:111702. https://doi.org/10.1016/j.envres.2021.111702
Leong YK, Chang JS (2020) Bioremediation of heavy metals using microalgae: recent advances and mechanisms. Biores Technol 303:122886. https://doi.org/10.1016/j.biortech.2020.122886
Pourrut B, Jean S, Silvestre J, Pinelli E (2011) Lead-induced DNA damage in Vicia faba root cells: potential involvement of oxidative stress. Mut Res Genet Toxicol Environ Mutagen 726(2):123–128. https://doi.org/10.1016/j.mrgentox.2011.09.001
Reuben A, Caspi A, Belsky DW, Broadbent J, Harrington H, Sugden K, Houts RM, Ramrakha S, Poulton R, Moffitt TE (2017) Association of childhood blood lead levels with cognitive function and socioeconomic status at age 38 years and with IQ change and socioeconomic mobility between childhood and adulthood. JAMA 317(12):1244–1251. https://doi.org/10.1001/jama.2017.1712
Cao J, Xie C, Hou Z (2022) Ecological evaluation of heavy metal pollution in the soil of Pb-Zn mines. Ecotoxicology 1–12. https://doi.org/10.1007/s10646-021-02505-3
Godwin HA (2001) The biological chemistry of lead. Curr Opin Chem Biol 5(2):223–227. https://doi.org/10.1016/S1367-5931(00)00194-0
Liu K, Li C, Tang S, Shang G, Yu F, Li Y (2020) Heavy metal concentration, potential ecological risk assessment and enzyme activity in soils affected by a lead-zinc tailing spill in Guangxi, China. Chemosphere 251:126415. https://doi.org/10.1016/j.chemosphere.2020.126415
Huang CY, Xu JM (2012) Soil science, third ed. China Agricultural, Beijing
Pourrut B, Shahid M, Dumat C, Winterton P, Pinelli E (2011) Lead uptake, toxicity, and detoxification in plants. Rev Environ Contam Toxicol 213:113–136. https://doi.org/10.1007/978-1-4419-9860-6_4
Wan Y, Devereux R, George SE, Chen J, Gao B, Noerpel M, Scheckel K (2022) Interactive effects of biochar amendment and lead toxicity on soil microbial community. J Hazard Mater 425:127921. https://doi.org/10.1016/j.jhazmat.2021.127921
Xu DM, Fu RB, Liu HQ, Guo XP (2021) Current knowledge from heavy metal pollution in Chinese smelter contaminated soils, health risk implications and associated remediation progress in recent decades: a critical review. J Clean Prod 286:124989. https://doi.org/10.1016/j.jclepro.2020.124989
Arvind K, Duraisamy R, Naveen K, Ravikant V, Agam K, Daneshver KV, Ilakiya J, Binny M, Krishna K J (2022) Investigation on the potential of eco-friendly bio-char for amendment in serpentine soils and immobilization of heavy metals contaminants: a review. Biomass Conversion and Biorefinery 1–21. https://doi.org/10.1007/s13399-021-02257-4
Liu L, Li W, Song W, Guo M (2018) Remediation techniques for heavy metal-contaminated soils: principles and applicability. Sci Total Environ 633:206–219. https://doi.org/10.1016/j.scitotenv.2018.03.161
Farrell M, Jones DL (2009) Use of composts in the remediation of heavy metal contaminated soil. J Hazard Mater 175(1–3):575–582. https://doi.org/10.1016/j.jhazmat.2009.10.044
Liu H, Xu F, Xie Y, Wang C, Zhang AK, Li LL, Xu H (2018) Effect of modified coconut shell biochar on availability of heavy metals and biochemical characteristics of soil in multiple heavy metals contaminated soil. Sci Total Environ 645:702–709. https://doi.org/10.1016/j.scitotenv.2018.07.115
Xia Y, Li Y, Sun Y, Miao W, Liu ZG (2021) Co-pyrolysis of corn stover with industrial coal ash for in situ efficient remediation of heavy metals in multi-polluted soil. Environ Pollut 289:117840. https://doi.org/10.1016/j.envpol.2021.117840
Wang Y, Tan R, Zhou L, Lian J, Wu X, He R, Yang F, He X, Zhu W (2021) Heavy metal fixation of lead-contaminated soil using Morchella mycelium. Environ Pollut 289:117829. https://doi.org/10.1016/j.envpol.2021.117829
Gao X, Tang X, Zhao K, Balan V, Zhu Q (2021) Biogas production from anaerobic co-digestion of spent mushroom substrate with different livestock manure. Energies 14(3):570. https://doi.org/10.3390/en14030570
Huang J, Liu J, Kuo J, Xie W, Zhang X, Chang K, Buyukada M, Evrendilek F (2019) Kinetics, thermodynamics, gas evolution and empirical optimization of (co-) combustion performances of spent mushroom substrate and textile dyeing sludge. Biores Technol 280:313–324. https://doi.org/10.1016/j.biortech.2019.02.011
Meng L, Li W, Zhang S, Wu C, Lv L (2017) Feasibility of co-composting of sewage sludge, spent mushroom substrate and wheat straw. Biores Technol 226:39–45. https://doi.org/10.1007/s11104-015-2487-4
Dong L, Jin Y, Song T, Liang J, Bai X, Yu S, Teng C, Wang X, Qu J, Huang X (2017) Removal of Cr (VI) by surfactant modified Auricularia auricula spent substrate: biosorption condition and mechanism. Environ Sci Pollut Res 24(21):17626–17641. https://doi.org/10.1007/s11356-017-9326-5
Hu X, Yan L, Gu H, Zang T, Jin Y, Qu J (2014) Biosorption mechanism of Zn2+ from aqueous solution by spent substrates of Pleurotus ostreatus. Korean J Chem Eng 31(11):1911–1918. https://doi.org/10.1007/s11814-014-0206-0
Qu J, Zang T, Gu H, Li K, Hu Y, Ren G, Xu X, Jin Y (2015) Biosorption of copper ions from aqueous solution by Flammulina velutipes spent substrate. BioResources 10(4):8058–8075. https://doi.org/10.15376/biores.10.4.8058-8075
Jin ZH, Zhang M, Li R, Zhang X, Wang GL, Liu XS, Qu JJ, Jin Y (2020) Spent mushroom substrate combined with alkaline amendment passivates cadmium and improves soil property. Environ Sci Pollut Res 27(14):16317–16325. https://doi.org/10.1007/s11356-020-08099-3
Kong Y, Ma R, Li G, Wang G, Liu Y, Yuan J (2022) Impact of biochar, calcium magnesium phosphate fertilizer and spent mushroom substrate on humification and heavy metal passivation during composting. Sci Total Environ 824:153755. https://doi.org/10.1016/j.scitotenv.2022.153755
Liu X, Bai X, Dong L, Liang J, Jin Y, Wei Y, Li Y, Huang S, Qu J (2018) Composting enhances the removal of lead ions in aqueous solution by spent mushroom substrate: biosorption and precipitation. J Clean Prod 200:1–11. https://doi.org/10.1016/j.jclepro.2018.07.182
Ministry of Ecological Environment, PR China (2018) Soil environmental quality-risk control standard for soil contamination of agricultural land (GB 15618–2018)
Wang Y, Guo D, Wang J, Tian B, Li Y, Sun G, Zhang H (2022) Exogenous melatonin alleviates NO2 damage in tobacco leaves by promoting antioxidant defense, modulating redox homeostasis, and signal transduction. J Hazard Mater 424:127265. https://doi.org/10.1016/j.jhazmat.2021.127265
Wang Y, Yu Y, Zhang H, Huo Y, Liu X, Che Y, Wang J, Sun G, Zhang H (2022) The phytotoxicity of exposure to two polybrominated diphenyl ethers (BDE47 and BDE209) on photosynthesis and the response of the hormone signaling and ROS scavenging system in tobacco leaves. J Hazard Mater 426:128012. https://doi.org/10.1016/j.jhazmat.2021.128012
Zhang H, Xu Z, Huo Y, Guo K, Wang Y, He G, Sun H, Li M, Li X, Xu N (2020) Overexpression of Trx CDSP32 gene promotes chlorophyll synthesis and photosynthetic electron transfer and alleviates cadmium-induced photoinhibition of PSII and PSI in tobacco leaves. J Hazard Mater 398:122899. https://doi.org/10.1016/j.jhazmat.2020.122899
National Health and Family Planning Commission, PR China (2017) National food safety standard-determination of lead in food (GB 5009.12–2017)
Liu X, Zhang X, Li R, Wang G, Jin Y, Xu W, Wang H, Qu J (2021) Organic amendment improves rhizosphere environment and shapes soil bacterial community in black and red soil under lead stress. J Hazard Mater 416:125805. https://doi.org/10.1016/j.jhazmat.2021.125805
Bao SD (2010) Soil agrochemical analysis method, third ed. China Agricultural, Beijing
Tessier A, Campbell PG, Bisson M (1979) Sequential extraction procedure for the speciation of particulate trace metals. Anal Chem 51(7):844–851
Environmental Protection Agency, PR China (1997) Soil quality-determination of lead, cadmium-graphite furnace atomic absorption spectrophotometry (GB/T 17141–1997)
Lin XG (2010) Principles and methods of soil microbial research. Higher Education Press, Beijing
Yu X, Li X, Ren C, Wang J, Wang C, Zou Y, Wang X, Li G, Li Q (2022) Co-composting with cow dung and subsequent vermicomposting improve compost quality of spent mushroom. Biores Technol 127386. https://doi.org/10.1016/j.biortech.2022.127386
Ahmad M, Lee SS, Yang JE, Ro H-M, Lee YH, Ok YS (2012) Effects of soil dilution and amendments (mussel shell, cow bone, and biochar) on Pb availability and phytotoxicity in military shooting range soil. Ecotoxicol Environ Saf 79:225–231. https://doi.org/10.1016/j.ecoenv.2012.01.003
Zhang Y, Deng B, Li Z (2018) Inhibition of NADPH oxidase increases defense enzyme activities and improves maize seed germination under Pb stress. Ecotoxicol Environ Saf 158:187–192. https://doi.org/10.1016/j.ecoenv.2018.04.028
Oukarroum A, El Madidi S, Strasser RJ (2016) Differential heat sensitivity index in barley cultivars (Hordeum vulgare L.) monitored by chlorophyll a fluorescence OKJIP. Plant Physiol Biochem 105:102–108. https://doi.org/10.1016/j.plaphy.2016.04.015
Oukarroum A, Goltsev V, Strasser RJ (2013) Temperature effects on pea plants probed by simultaneous measurements of the kinetics of prompt fluorescence, delayed fluorescence and modulated 820 nm reflection. PLoS ONE 8(3):e59433. https://doi.org/10.1371/journal.pone.0059433
Groom QJ, Baker NR (1992) Analysis of light-induced depressions of photosynthesis in leaves of a wheat crop during the winter. Plant Physiol 100(3):1217–1223. https://doi.org/10.1104/pp.100.3.1217
Appenroth KJ, Stockel J, Srivastava A, Strasser R (2001) Multiple effects of chromate on the photosynthetic apparatus of Spirodela polyrhiza as probed by OJIP chlorophyll a fluorescence measurements. Environ Pollut 115(1):49–64. https://doi.org/10.1016/S0269-7491(01)00091-4
Van Heerden PD, Strasser RJ, Kruger GH (2004) Reduction of dark chilling stress in N-2-fixing soybean by nitrate as indicated by chlorophyll a fluorescence kinetics. Physiol Plant 121(2):239–249. https://doi.org/10.1111/j.0031-9317.2004.0312.x
Li R, Tan W, Wang G, Zhao X, Dang Q, Yu H, Xi B (2019) Nitrogen addition promotes the transformation of heavy metal speciation from bioavailable to organic bound by increasing the turnover time of organic matter: an analysis on soil aggregate level. Environ Pollut 255:113170. https://doi.org/10.1016/j.envpol.2019.113170
Yu H, Liu P, Shan W, Teng Y, Rao D, Zou L (2021) Remediation potential of spent mushroom substrate on Cd pollution in a paddy soil. Environ Sci Pollut Res 28(27):36850–36860. https://doi.org/10.1007/s11356-021-13266-1
Burke IC, Thomas WE, Spears JF, Wilcut JW (2003) Influence of environmental factors on after-ripened crowfootgrass (Dactyloctenium aegyptium) seed germination. Weed Sci 51(3):342–347. https://doi.org/10.1614/0043-1745(2003)051[0342:IOEFOA]2.0.CO;2
Ma H, Yang H, Lu X, Pan Y, Wu H, Liang Z, Ooi MK (2015) Does high pH give a reliable assessment of the effect of alkaline soil on seed germination? A case study with Leymus chinensis (Poaceae). Plant Soil 394(1):35–43. https://doi.org/10.1007/s11104-015-2487-4
Bishop PL, Godfrey C (1983) Nitrogen transformations during sludge composting. Biocycle 24:34–39
Lu JL (2003) Plant nutrition (volume 1), second ed. China Agricultural, Beijing
Chen L, Jiang Y, Liang C, Luo Y, Xu Q, Han C, Zhao Q, Sun B (2019) Competitive interaction with keystone taxa induced negative priming under biochar amendments. Microbiome 7(1):1–18. https://doi.org/10.1186/s40168-019-0693-7
Qin C, Yuan X, Xiong T, Tan YZ, Wang H (2020) Physicochemical properties, metal availability and bacterial community structure in heavy metal-polluted soil remediated by montmorillonite-based amendments. Chemosphere 261:128010. https://doi.org/10.1016/j.chemosphere.2020.128010
Xiao S, Zhang Q, Chen X, Dong F, Chen H, Liu M, Ali I (2019) Speciation distribution of heavy metals in uranium mining impacted soils and impact on bacterial community revealed by high-throughput sequencing. Front Microbiol 1867. https://doi.org/10.3389/fmicb.2019.01867
Ibekwe A, Poss J, Grattan S, Grieve C, Suarez D (2010) Bacterial diversity in cucumber (Cucumis sativus) rhizosphere in response to salinity, soil pH, and boron. Soil Biol Biochem 42(4):567–575. https://doi.org/10.1016/j.soilbio.2009.11.033
Lian T, Yu Z, Liu J, Li Y, Wang G, Liu X, Herbert SJ, Wu J, Jin J (2018) Rhizobacterial community structure in response to nitrogen addition varied between two Mollisols differing in soil organic carbon. Sci Rep 8(1):1–8. https://doi.org/10.1038/s41598-018-30769-z
Zeng J, Liu X, Song L, Lin X, Zhang H, Shen C, Chu H (2016) Nitrogen fertilization directly affects soil bacterial diversity and indirectly affects bacterial community composition. Soil Biol Biochem 92:41–49. https://doi.org/10.1016/j.soilbio.2015.09.018
Kim JJ, Alkawally M, Brady AL, Rijpstra WIC, Damste JSS, Dunfield PF (2013) Chryseolinea serpens gen. nov., sp. nov., a member of the phylum Bacteroidetes isolated from soil. Int J Syst Evol Microbiol 63 (Pt_2):654–660. https://doi.org/10.1099/ijs.0.039404-0
Visioli G, Sanangelantoni AM, Vamerali T, Dal Cortivo C, Blandino M (2018) 16S rDNA profiling to reveal the influence of seed-applied biostimulants on the rhizosphere of young maize plants. Molecules 23(6):1461. https://doi.org/10.3390/molecules23061461
Nedashkovskaya OI, Vancanneyt M, Kim SB, Han J, Zhukova NV, Shevchenko LS (2010) Salinimicrobium marinum sp. nov., a halophilic bacterium of the family Flavobacteriaceae, and emended descriptions of the genus Salinimicrobium and Salinimicrobium catena. Int J Syst Evol Microbiol 60 (10):2303–2306. https://doi.org/10.1099/ijs.0.019166-0
Starke R, Bastida F, Abadia J, Garcia C, Nicolas E, Jehmlich N (2017) Ecological and functional adaptations to water management in a semiarid agroecosystem: a soil metaproteomics approach. Sci Rep 7(1):1–16. https://doi.org/10.1038/s41598-017-09973-w
Teng T, Liang J, Wu Z (2021) Identification of pyrene degraders via DNA-SIP in oilfield soil during natural attenuation, bioaugmentation and biostimulation. Sci Total Environ 800:149485. https://doi.org/10.1016/j.scitotenv.2021.149485
Teramoto M, Suzuki M, Hatmanti A, Harayama S (2010) The potential of Cycloclasticus and Altererythrobacter strains for use in bioremediation of petroleum-aromatic-contaminated tropical marine environments. J Biosci Bioeng 110(1):48–52. https://doi.org/10.1016/j.jbiosc.2009.12.008
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Juanjuan Qu was responsible for conceptualization including ideas, formulation of overarching research goals and aims.
Yaru Yuan was responsible for preparation, creation, and presentation of the published work, specifically writing the initial and revised manuscript.
Lin Zhu was responsible for the preparation of reagents, instrumentation, computing resources, and other analysis tools.
Yu Jin was responsible for conducting a research and investigation process, specifically performing the experiments data.
Xiuhong Xu was responsible for supervision the research activity planning and execution.
Xuesheng Liu has participated in the data analysis and applied statistical and mathematical techniques to analyze the research data.
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Yuan, Y., Zhu, L., Jin, Y. et al. Comprehensive evaluation of the remediation efficacy of composted and uncomposted mushroom substrate on lead-contaminated soil. Biomass Conv. Bioref. (2022). https://doi.org/10.1007/s13399-022-03370-8
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DOI: https://doi.org/10.1007/s13399-022-03370-8