Effect of Fresh Organic Matter of Straw on Microbiological Parameters of Sod-Podzolic Soil
- Authors: Nikitin D.A.1, Semenov M.V.1, Ksenofontova N.A.1, Tkhakakhova A.K.1, Rusakova I.V.2, Lukin S.M.2
-
Affiliations:
- Dokuchaev soil science institute
- All-Russian Research Institute of Organic Fertilizers and Peat
- Issue: No 5 (2023)
- Pages: 640-653
- Section: СЕЛЬСКОХОЗЯЙСТВЕННАЯ МИКРОБИОЛОГИЯ
- URL: https://journals.rcsi.science/0032-180X/article/view/138089
- DOI: https://doi.org/10.31857/S0032180X22601189
- EDN: https://elibrary.ru/IEEOCD
- ID: 138089
Cite item
Abstract
The loss of soil organic matter (SOM) due to agricultural land use has a negative impact on soil properties and is one of the major contributors to the increase in atmospheric CO2 concentrations. An appropriate way for simultaneous restoration of POM stocks and deposition of sequestered carbon is the straw application to the soil. The aim of the study was to evaluate the effect of straw on the quantitative indicators of different groups of microorganisms in sod-podzolic soil (Umbric Retisol) in a long-term field experiment. Introduction of straw increased microbial biomass carbon (Cmic) by 1.25–2 times, with the greatest increase in microbial biomass observed in the variants without fertilizer. Basal respiration and respiration coefficient (qCO2) increased in the row: control < NPK < NPK + straw < straw. Application of straw increased the gene copy number of fungi and bacteria up to 2 times and archaea up to 1.5 times. Mineral fertilizer application without straw reduced qCO2, fungi biomass and archaeal gene copy number by 1.5–3.0 times. The fungi/bacteria ratio varied from 4 to 15 determined by fluorescent microscopy and from 0.17 to 0.33 by quantitative PCR. The lowest values of fungi/bacteria ratios were found in soils with the application of mineral fertilizers, and the highest – with the incorporation of straw. Thus, the regular introduction of fresh organic matter of straw is an important technological procedure to increase the microbiological activity of soil and leveling the negative impact of mineral fertilizers on soil microbiota.
About the authors
D. A. Nikitin
Dokuchaev soil science institute
Author for correspondence.
Email: dimnik90@mail.ru
Russia, 119017, Moscow
M. V. Semenov
Dokuchaev soil science institute
Email: dimnik90@mail.ru
Russia, 119017, Moscow
N. A. Ksenofontova
Dokuchaev soil science institute
Email: dimnik90@mail.ru
Russia, 119017, Moscow
A. K. Tkhakakhova
Dokuchaev soil science institute
Email: dimnik90@mail.ru
Russia, 119017, Moscow
I. V. Rusakova
All-Russian Research Institute of Organic Fertilizers and Peat
Email: dimnik90@mail.ru
Russia, 601390, Vyatkino
S. M. Lukin
All-Russian Research Institute of Organic Fertilizers and Peat
Email: dimnik90@mail.ru
Russia, 601390, Vyatkino
References
- Ананьева Н.Д., Благодатская Е.В., Демкина Т.С. Оценка устойчивости микробных комплексов к природным и антропогенным воздействиям // Почвоведение. 2002. № 5. С. 580–587.
- Ананьева Н.Д., Стольникова Е.В., Сусьян Е.А., Ходжаева А.К. Грибная и бактериальная микробная биомасса (селективное ингибирование) и продуцирование CO2 и N2O дерново-подзолистыми почвами постагрогенных биогеоценозов // Почвоведение. 2010. № 11. С. 1387–1393.
- Ананьева Н.Д., Сусьян Е.А., Гавриленко Е.Г. Особенности определения углерода микробной биомассы почвы методом субстрат-индуцированного дыхания // Почвоведение. 2011. № 11. С. 1327–1333.
- Благодатская Е.В., Семенов М.В., Якушев А.В. Активность и биомасса почвенных микроорганизмов в изменяющихся условиях окружающей среды. М.: Товарищество научных изданий КМК, 2016.
- Звягинцев Д.Г. Методы почвенной микробиологии и биохимии. М.: Изд-во Моск. ун-та, 1991. 302 с.
- Лаврентьева Е.В., Семенов А.М., Зеленев В.В., Чжун Ю., Семенова Е.В., Семенов В.М., Намсараев Б.Б., Ван Бругген А.К.Х. Ежедневная динамика целлюлазной активности в пахотной почве в зависимости от обработки // Почвоведение. 2009. № 8. С. 952–961.
- Лукин С.М. История научных исследований по плодородию почв и применению удобрений (к 105-летию с образования Судогодского опытного поля ФГБНУ ВНИИОУ) // История науки и техники. 2018. № 3. С. 3–17.
- Никитин Д.А., Чернов Т.И., Железова А.Д., Тхакахова А.К., Никитина С.А., Семенов М.В., Ксенофонтова Н.А., Кутовая О.В. Сезонная динамика биомассы микроорганизмов в дерново-подзолистой почве // Почвоведение. 2019. № 11. С. 1356–1364. https://doi.org/10.1134/S0032180X19110078
- Никитин Д.А., Иванова Е.А., Железова А.Д., Семенов М.В., Гаджиумаров Р.Г., Тхакахова А.К., Чернов Т.И., Ксенофонтова Н.А., Кутовая О.В. Оценка влияния технологии no-till и вспашки на микробиом южных агрочерноземов // Почвоведение. 2020. № 12. С. 1508–1520. https://doi.org/10.31857/S0032180X20120084
- Никитин Д.А., Семенов М.В., Чернов Т.И., Ксенофонтова Н.А., Железова А.Д., Иванова Е.А., Хитров Н.Б., Степанов А.Л. Микробиологические индикаторы экологических функций почв (обзор) // Почвоведение. 2022. № 2. С. 228–243. https://doi.org/10.31857/S0032180X22020095
- Полянская Л.М., Звягинцев Д.Г. Содержание и структура микробной биомассы как показатель экологического состояния почв // Почвоведение. 2005. № 6. С. 706–714.
- Полянская Л.М., Суханова Н.И., Чакмазян К.В., Звягинцев Д.Г. Особенности изменения структуры микробной биомассы почв в условиях залежи // Почвоведение. 2012. № 7. С. 792–792.
- Полянская Л.М., Юмаков Д.Д., Тюгай З.Н., Степанов А.Л. Соотношение грибов и бактерий в темногумусовой лесной почве // Почвоведение. 2020. № 9. С. 1094–1099. https://doi.org/10.31857/S0032180X20090129
- Русакова И.В. Влияние соломы зерновых и зернобобовых культур на содержание углерода, агрохимические свойства и баланс элементов питания в дерново-подзолистой почве // Агрохимический вестник. 2015. № 6. С. 6–10.
- Русакова И.В. Микробиологические и экофизиологические параметры дерново-подзолистой почвы при длительном применении соломы и минеральных удобрений, их связь с урожайностью // Сельскохозяйственная биология. 2020. № 55(1). С. 153–162. https://doi.org/10.15389/agrobiology.2020.1.153rus
- Семенов B.М., Ходжаева А.К. Агроэкологические функции растительных остатков в почве // Агрохимия. 2006. № 7. С. 63–81.
- Семенов В.М., Когут Б.М. Почвенное органическое вещество. М.: ГЕОС, 2015. 233 с.
- Семенов В.М., Паутова Н.Б., Лебедева Т.Н., Хромычкина Д.П., Семенов Н.А., Лопес де Гереню В.О. Разложение растительных остатков и формирование активного органического вещества в почве инкубационных экспериментов // Почвоведение. 2019. № 10. С. 1172–1184. https://doi.org/10.1134/S0032180X19100113
- Семенов М.В. Метабаркодинг и метагеномика в почвенно-экологических исследованиях: успехи, проблемы и возможности // Журн. общ. биологии. 2019. № 80(6). С. 403–417. https://doi.org/10.1134/S004445961906006X
- Семенов М.В., Никитин Д.А., Степанов А.Л., Семенов В.М. Структура бактериальных и грибных сообществ ризосферного и внекорневого локусов серой лесной почвы // Почвоведение. 2019. № 3. С. 355–369. https://doi.org/10.1134/S0032180X19010131
- Семенов М.В., Манучарова Н.А., Краснов Г.С., Никитин Д.А., Степанов А.Л. Биомасса и таксономическая структура микробных сообществ в почвах правобережья р. Оки // Почвоведение. 2019. № 8. С. 974–985. https://doi.org/10.1134/S0032180X19080124
- Чернов Т.И., Семенов М.В. Управление почвенными микробными сообществами: возможности и перспективы (обзор) // Почвоведение. 2021. № 12. С. 1506–1522.
- Angst G., Mueller K.E., Nierop K.G., Simpson M.J. Plant-or microbial-derived? A review on the molecular composition of stabilized soil organic matter // Soil Biol. Biochem. 2021. V. 156. P. 108189. https://doi.org/10.1016/j.soilbio.2021.108189
- Bailey V.L., Smith J.L., Bolton H., Jr. Fungal-to-bacterial ratios in soils investigated for enhanced C sequestration // Soil Biol. Biochem. 2002. V. 34. P. 997–1007. https://doi.org/10.1016/S0038-0717(02)00033-0
- Berhane M., Xu M., Liang Z., Shi J., Wei G., Tian X. Effects of long-term straw return on soil organic carbon storage and sequestration rate in North China upland crops: A meta-analysis // Global Change Biol. 2020. V. 26. P. 2686–2701. https://doi.org/10.1111/gcb.15018
- Chen X., Liu M., Kuzyakov Y., Li W., Liu J., Jiang C., Meng Wu, Li Z. Incorporation of rice straw carbon into dissolved organic matter and microbial biomass along a 100-year paddy soil chronosequence // Appl. Soil Ecol. 2018. V. 130. P. 84–90. https://doi.org/10.1016/j.apsoil.2018.06.004
- Chen X., Xia Y., Rui Y., Ning Z., Hu Y., Tang H., He H., Li H., Kuzyakov Y., Ge T., Wu J., Su Y. Microbial carbon use efficiency, biomass turnover, and necromass accumulation in paddy soil depending on fertilization // Agriculture, Ecosystems Environment. 2020. V. 292. P. 106816. https://doi.org/10.1016/j.agee.2020.106816
- Craine J., Elmore A.J., Wang L., Aranibar J., Bauters M., Boeckx P. et al. Isotopic evidence for oligotrophication of terrestrial ecosystems // Nature Ecology and Evolution. 2018. V. 2. P. 1735–1744.
- Fan F., Yu B., Wang B., George T.S., Yin H., Xu D., Li D., Song A. Microbial mechanisms of the contrast residue decomposition and priming effect in soils with different organic and chemical fertilization histories // Soil Biol. Biochem. 2019. V. 135. P. 213–221. https://doi.org/10.1016/j.soilbio.2019.05.001
- Francioli D., Schulz E., Lentendu G., Wubet T., Buscot F., Reitz T. Mineral vs. organic amendments: microbial community structure, activity and abundance of agriculturally relevant microbes are driven by long-term fertilization strategies // Frontiers in Microbiology. 2016. V. 7. P. 1446. https://doi.org/10.3389/fmicb.2016.01446
- Han P., Zhang W., Wang G., Sun W., Huang Y. Changes in soil organic carbon in croplands subjected to fertilizer management: a global meta-analysis // Scientific Reports. 2016. V. 6(1). P. 1–13. https://doi.org/10.1038/srep27199
- He J.Z., Hu H.W., Zhang L.M. Current insights into the autotrophic thaumarchaeal ammonia oxidation in acidic soils // Soil Biol. Biochem. 2012. V. 55. P. 146–154. https://doi.org/10.1016/j.soilbio.2012.06.006
- He M., Ma W., Zelenev V.V., Khodzaeva A.K., Kuznetsov A.M., Semenov A.M., Semenov V.M., Blok W.W., van Bruggen A.H.C. Short-term dynamics of greenhouse gas emissions and cultivable bacterial populations in response to induced and natural disturbances in organically and conventionally managed soils // Appl. Soil Ecol. 2017. V. 119. P. 294–306. https://doi.org/10.1016/j.apsoil.2017.07.011
- Heděnec P., Nilsson L.O., Zheng H., Gundersen P., Schmidt I.K., Rousk J., Vesterdal L. Mycorrhizal association of common European tree species shapes biomass and metabolic activity of bacterial and fungal communities in soil // Soil Biol. Biochem. 2020. V. 149. P. 107933. https://doi.org/10.1016/j.soilbio.2020.107933
- Geisseler D., Scow K.M. Long-term effects of mineral fertilizers on soil microorganisms – A review // Soil Biol. Biochem. 2014. V. 75. P. 54–63. https://doi.org/10.1016/j.soilbio.2014.03.023
- Geng Y., Cao G., Wang L., Wang S. Effects of equal chemical fertilizer substitutions with organic manure on yield, dry matter, and nitrogen uptake of spring maize and soil nitrogen distribution // PloS One. 2019. V. 14. P. e0219512. https://doi.org/10.1371/journal.pone.0219512
- Jin Z., Shah T., Zhang L., Liu H., Peng S., Nie L. Effect of straw returning on soil organic carbon in rice–wheat rotation system: A review // Food and Energy Security. 2020. V. 9(2). P. e200. https://doi.org/10.1002/fes3.200
- Iovieno P., Morra L., Leone A., Pagano L., Alfani A. Effect of organic and mineral fertilizers on soil respiration and enzyme activities of two Mediterranean horticultural soils // Biol. Fertil. Soils. 2009. V. 45. P. 555–561. https://doi.org/10.1007/s00374-009-0365-z
- Landenmark H.K., Forgan D.H., Cockell C.S. An estimate of the total DNA in the biosphere // PLoS Biology. 2015. V. 13. P. e1002168. https://doi.org/10.1371/journal.pbio.1002168
- Liang Y., Al-Kaisi M., Yuan J., Liu J., Zhang H., Wang L., Cai H., Ren J. Effect of chemical fertilizer and straw-derived organic amendments on continuous maize yield, soil carbon sequestration and soil quality in a Chinese Mollisol // Agriculture, Ecosystems Environment. 2021. V. 314. P. 107403. https://doi.org/10.1016/j.agee.2021.107403
- Liu C., Lu M., Cui J., Li B., Fang C. Effects of straw carbon input on carbon dynamics in agricultural soils: a meta-analysis // Global Change Biology. 2014. V. 20. P. 1366–1381. https://doi.org/10.1111/gcb.12517
- Lu F. How can straw incorporation management impact on soil carbon storage? A meta-analysis // Mitigation and Adaptation Strategies for Global Change. 2015. V. 20. P. 1545–1568. https://doi.org/10.1007/s11027-014-9564-5
- Malik A.A., Chowdhury S., Schlager V., Oliver A., Puissant J., Vazquez P.G., Jehmlich N., Bergen M., Griffiths R.I., Gleixner G. Soil fungal: bacterial ratios are linked to altered carbon cycling // Frontiers in Microbiology. 2016. V. 7. P. 1247. https://doi.org/10.3389/fmicb.2016.01247
- Morais M.C., Ferrari B.M., Borges C.D., Cherubin M.R., Tsai S.M., Cerri C.C., Cerri C.E.P, Feigl B.J. Does sugarcane straw removal change the abundance of soil microbes? // BioEnergy Research. 2019. V. 12. P. 901–908. https://doi.org/10.1007/s12155-019-10018-5
- Saleem M., Law A.D., Sahib M.R., Pervaiz Z.H., Zhang Q. Impact of root system architecture on rhizosphere and root microbiome // Rhizosphere. 2018. V. 6. P. 47–51. https://doi.org/10.1016/j.rhisph.2018.02.003
- Semenov M.V., Krasnov G.S., Semenov V.M., van Bruggen A.H. Long-term fertilization rather than plant species shapes rhizosphere and bulk soil prokaryotic communities in agroecosystems // Appl. Soil Ecol. 2020. V. 154. P. 103641. https://doi.org/10.1016/j.apsoil.2020.103641
- Semenov M.V., Krasnov G.S., Semenov V.M., Ksenofontova N., Zinyakova N.B., van Bruggen A.H. Does fresh farmyard manure introduce surviving microbes into soil or activate soil-borne microbiota? // J. Environ. Managem. 2021. V. 294. P. 113018.
- Semenov M.V., Krasnov G.S., Semenov V.M., van Bruggen A. Mineral and organic fertilizers distinctly affect fungal communities in the crop rhizosphere // J. Fungi. 2022. V. 8. P. 251. https://doi.org/10.3390/jof8030251
- Six J., Frey S.D., Thiet R.K., Batten K.M. Bacterial and fungal contributions to carbon sequestration in agroecosystems // Soil Sci. Soc. Am. J. 2006. V. 70(2). P. 555–569. https://doi.org/10.2136/sssaj2004.0347
- Soares M., Rousk J. Microbial growth and carbon use efficiency in soil: Links to fungal-bacterial dominance, SOC-quality and stoichiometry // Soil Biol. Biochem. 2019. V. 131. P. 195–205. https://doi.org/10.1016/j.soilbio.2019.01.010
- Suzuki M.T., Taylor L.T., DeLong E.F. Quantitative analysis of small-subunit rRNA genes in mixed microbial populations via 5′-nuclease assays // Appl. Environ. Microbiol. 2000. V. 66(11). P. 4605–4614. https://doi.org/10.1128/AEM.66.11.4605-4614.2000
- Tiefenbacher A., Sandén T., Haslmayr H.-P., Miloczki J., Wenzel W., Spiegel H. Optimizing Carbon Sequestration in Croplands: A Synthesis // Agronomy. 2021. V. 11. P. 882. https://doi.org/10.3390/agronomy11050882
- van Bruggen A.H.C., He M., Zelenev V.V., Semenov V.M., Semenov A.M., Semenova E.V., Kuznetsova T.V., Khodzaeva A.K., Kuznetsov A.M., Semenov M.V. Relationships between greenhouse gas emissions and cultivable bacterial populations in conventional, organic and long-term grass plots as affected by environmental variables and disturbances // Soil Biol. Biochem. 2017. V. 114. P. 145–159. https://doi.org/10.1016/j.soilbio.2017.07.014
- Wang D., Zhu Z., Shahbaz M., Chen L., Liu S., Inubushi K., Wu J., Ge T. Split N and P addition decreases straw mineralization and the priming effect of a paddy soil: a 100-day incubation experiment // Biol. Fertil. Soils. 2019. V. 55. P. 701–712. https://doi.org/10.1007/s00374-019-01383-6
- Wang Y., Wu P., Mei F., Ling Y., Qiao Y., Liu C., Legharic S.J., Guan X., Wang T. Does continuous straw returning keep China farmland soil organic carbon continued increase? A meta-analysis // J. Environ. Management. 2021. V. 288. P. 112391. https://doi.org/10.1016/j.jenvman.2021.112391
- Wessén E., Nyberg K., Jansson J.K., Hallin S. Responses of bacterial and archaeal ammonia oxidizers to soil organic and fertilizer amendments under long-term management // Appl. Soil Ecol. 2010. V. 45. P. 193–200. https://doi.org/10.1016/j.apsoil.2010.04.003
- Wu L., Zhang W., Wei W., He Z., Kuzyakov Y., Bol R., Hu R. Soil organic matter priming and carbon balance after straw addition is regulated by long-term fertilization // Soil Biol. Biochem. 2019. V. 135. P. 383–391. https://doi.org/10.1016/j.soilbio.2019.06.003
- Yan D., Long X.E., Ye L., Zhang G., Hu A., Wang D., Ding S. Effects of salinity on microbial utilization of straw carbon and microbial residues retention in newly reclaimed coastal soil // Eur. J. Soil Biol. 2021. V. 107. P. 103364. https://doi.org/10.1016/j.ejsobi.2021.103364
- Yang H., Fang C., Meng Y., Dai Y., Liu J. Long-term ditch-buried straw return increases functionality of soil microbial communities // Catena. 2021. V. 202. P. 105316. https://doi.org/10.1016/j.catena.2021.105316
- Yansheng C., Fengliang Z., Zhongyi Z., Tongbin Z., Huayun X. Biotic and abiotic nitrogen immobilization in soil incorporated with crop residue // Soil Till. Res. 2020. V. 202. P. 104664. https://doi.org/10.1016/j.still.2020.104664
- Zhao X.M., He L., Zhang Z.D., Wang H.B., Zhao L.P. Simulation of accumulation and mineralization (CO2 release) of organic carbon in chernozem under different straw return ways after corn harvesting // Soil Till. Res. 2016. V. 156. P. 148–154. https://doi.org/10.1016/j.still.2015.11.001
- Zhao M., Zhao J., Yuan J., Hale L., Wen T., Huang Q., Vivanco J.M., Zhou J., Kowalchuk G.A., Shen Q. Root exudates drive soil-microbe-nutrient feedbacks in response to plant growth // Plant, Cell Environ. 2021. V. 44. P. 613–628. https://doi.org/10.1111/pce.13928
- Zhu L.Q., Li J., Tao B.R., Hu N.J. Effect of different fertilization modes on soil organic carbon sequestration in paddy fields in South China: A meta-analysis // Ecol. Indic. 2015. V. 53. P. 144–153. https://doi.org/10.1016/j.ecolind.2015.01.038