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Assessment of Soil Specific Enzyme Activities in Aggregates Size Fractions: a Case Study from Subtropical Agro-ecosystem

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Abstract

Soil enzyme activities are closely associated with soil organic carbon (SOC) or microbial biomass carbon (MBC). High correlation between SOC and MBC masks their individual effects on enzyme activities. Expressing soil enzymes activity relative to soil organic carbon (SOC) or Microbial Biomass Carbon (MBC) would normalize the differences in SOC/MBC. A long term subtropical rice-wheat system was selected to study the variation in soil-specific enzyme activity (per unit SOC and MBC) in soil aggregates under integrated nutrient management. Soil organic carbon, microbial biomass carbon and the enzyme activities like acid phosphatase (ACP), alkaline phosphatase (AKP), dehydrogenase (DHA), fluorescien diacetate hydrolysing capacity (FDA) and urease were measured in three aggregate size fractions viz., >2000, 2000–250 and <250 µm. Integrated nutrient management practices significantly increased the specific enzyme activities expressed in relation to SOC and MBC. Aggregate size fractions of 2000–250 µm size exhibited higher specific enzyme activities, when expressed in terms of SOC. Enzyme activity (per unit MBC) in aggregates also followed the same pattern with an exception to dehydrogenase activity which was almost uniform across all the aggregates size fractions. Aggregates of larger size do not always possess higher enzymes activity; even smaller macroaggregates were able to retain stable extracellular enzyme activity per unit of SOC or MBC. This study opens an alley to express soil enzymatic activities relative to SOC or MBC level in the soils, rather than expressing absolute activities.

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DATA AVAILABILITY

The primary data is available with the corresponding author and can be shared, if so needed.

REFERENCES

  1. W. Ali, M. Nadeem, W. Ashiq, M. Zaeem, S. S. M. Gilani, S. Rajabi-Khamseh, T. H. Pham, V. Kavanagh, R. Thomas, and M. Cheema, “The effects of organic and inorganic phosphorus amendments on the biochemical attributes and active microbial population of agriculture podzols following silage corn cultivation in boreal climate,” Sci. Rep. 9, 17297 (2019). https://doi.org/10.1038/s41598-019-53906-8

    Article  CAS  Google Scholar 

  2. S. D. Allison and J. D. Jastrow, “Activities of extracellular enzymes in physically isolated fractions of restored grassland soils,” Soil Biol. Biochem. 38 (11), 3245–3256 (2006). https://doi.org/10.1016/j.soilbio.2006.04.011

    Article  CAS  Google Scholar 

  3. V. J. Allison, L. M. Condron, D. A. Peltzer, S. J. Richardson, and B. L. Turner, “Changes in enzyme activities and soil microbial community composition along carbon and nutrient gradients at the Franz Josef chronosequence, New Zealand,” Soil Biol. Biochem. 39 (7), 1770–1781 (2007). https://doi.org/10.1016/j.soilbio.2007.02.006

    Article  CAS  Google Scholar 

  4. A. Beheshti, F. Raiesi, and A. Golchin, “Soil properties, C fractions and their dynamics in land use conversion from native forests to croplands in northern Iran,” Agric., Ecosyst. Environ. 148, 121–133 (2012). https://doi.org/10.1016/j.agee.2011.12.001

    Article  Google Scholar 

  5. C. J. Bronick and R. Lal, “Soil structure and management: a review,” Geoderma 124, 3–22 (2005). https://doi.org/10.1016/j.geoderma.2004.03.005

    Article  CAS  Google Scholar 

  6. G. Csitari, Z. Tóth, and M. Kökény, “Effects of organic amendments on soil aggregate stability and microbial biomass in a long-term fertilization experiment (Iosdv),” Sustainability 13, 9769 (2021). https://doi.org/10.3390/su13179769

    Article  CAS  Google Scholar 

  7. A. Das, R. P. Sharma, N. Chattopadhyaya, and R. Rakshit. “Yield trends and nutrient budgeting under a long-term (28 years) nutrient management in rice-wheat cropping system under subtropical climatic condition,” Plant Soil Environ. 60, 351–357 (2014).  https://doi.org/10.17221/46/2014-PSE

    Article  Google Scholar 

  8. R. P. Dick, “Soil enzyme activities as indicators of soil quality,” in Defining Soil Quality for a Sustainable Environment, Ed. by J. W. Doran, D. C. Coleman, D. F. Bezdicek, and B. A. Stewart (Am. Soc. Agron., 1994), pp. 107–124. https://doi.org/10.2136/sssaspecpub35.c7

  9. X. Ding and X. Han, “Effects of long-term fertilization on contents and distribution of microbial residues within aggregate structures of a clay soil,” Biol. Fertil. Soils 50, 549–554 (2014). https://doi.org/10.1007/s00374-013-0867-6

    Article  Google Scholar 

  10. E. T. Elliott and D. C. Coleman, “Let the soil work for us,” Ecol. Bull. 39, 23–32 (1988). https://www.jstor.org/stable/20112982

    Google Scholar 

  11. V. S. Green, D. E. Stott, and M. Diack, “Assay for fluorescein diacetate hydrolytic activity: optimization for soil samples,” Soil Biol. Biochem. 38, 693–701 (2006). https://doi.org/10.1016/j.soilbio.2005.06.020

    Article  CAS  Google Scholar 

  12. K. A. Gomez and A. A. Gomez, Statistical Procedures for Agricultural Research (John Wiley & Sons, New York, 1984).

    Google Scholar 

  13. J. D. Jastrow, J. E. Amonette, and V. L. Bailey, “Mechanisms controlling soil carbon turnover and their potential application for enhancing carbon sequestration,” Clim. Change 80 (1–2), 5–23 (2007). https://doi.org/10.1007/s10584-006-9178-3

    Article  CAS  Google Scholar 

  14. D. A. Klein, T. C. Loh, and R. L. Goulding, “A rapid procedure to evaluate dehydrogenase activity of soils low in organic matter,” Soil Biol. Biochem. 3, 385–387 (1971). https://doi.org/10.1016/0038-0717(71)90049-6

    Article  CAS  Google Scholar 

  15. D. Kumar, R. Rakshit, R. Rani, P. Bharti, A. Das, and M. Kundu, “Integrated nutrient management in coconut (Cocos nucifera L.): an assessment of soil chemical and biological parameters under subtropical humid climate,” J. Soil Sci. Plant Nutr. 22, 2695–2706 (2022). https://doi.org/10.1007/s42729-022-00837-5

    Article  CAS  Google Scholar 

  16. R. Kumari, M. Kundu, A. Das, R. Rakshit, S. Sengupta, S. Sahay, and F. Ahmad, “Long term integrated nutrient management improves carbon stock and fruit yield in a subtropical mango (Mangifera indica L.) orchard,” J. Soil Sci. Plant Nutr. 20, 725–737 (2020). https://doi.org/10.1007/s42729-019-00160-6

    Article  CAS  Google Scholar 

  17. Y. Kuzyakov, “Priming effects: interactions between living and dead organic matter,” Soil Biol. Biochem. 42, 1363–1371 (2010). https://doi.org/10.1016/j.soilbio.2010.04.003

    Article  CAS  Google Scholar 

  18. A. Lagomarsino, A. Benedetti, S. Marinari, L. Pompili, M. C. Moscatelli, P. P. Roggero, R. Lai, L. Ledda, and S. Grego, “Soil organic C variability and microbial functions in a Mediterranean agro-forest ecosystem,” Biol. Fertil. Soils 47, 283–291 (2011). https://doi.org/10.1007/s00374-010-0530-4

    Article  Google Scholar 

  19. L. Landi, G. Renella, J. L. Moreno, L. Falchini, and P. Nannipieri, “Influence of cadmium on the metabolic quotient, l-:d-glutamic acid respiration ratio and enzyme activity: microbial biomass ratio under laboratory conditions,” Biol. Fertil. Soils 32, 8–16 (2000). https://doi.org/10.1007/s003740000205

    Article  CAS  Google Scholar 

  20. M. E. Malobane, A. D. Nciizah, F. N. Mudau, and I. I. Wakindiki, “Tillage, crop rotation and crop residue management effects on nutrient availability in a sweet sorghum-based cropping system in marginal soils of South Africa,” Agronomy 10 (6), 776 (2020). https://doi.org/10.3390/agronomy10060776

    Article  CAS  Google Scholar 

  21. P. Nannipieri, L. Giagoni, G. Renella, E. Puglisi, B. Ceccanti, G. Masciandaro, F. Fornasier, M. C. Moscatelli, and S. Marinari, “Soil enzymology: classical and molecular approaches,” Biol. Fertil. Soils 48, 743–762 (2018). https://doi.org/10.1007/s00374-012-0723-0

    Article  Google Scholar 

  22. P. Nannipieri, E. Kandeler, and P. Ruggiero, “Enzyme activities and microbiological and biochemical processes in soil,” in Enzymes in the Environment: Activity, Ecology and Applications, Ed. by R. G. Burns and R. P. Dick (Marcel Dekker, New York, 2002), pp. 1–33.

    Google Scholar 

  23. J. H. Quastel, Soil Metabolism (The Royal Institute of Chemistry of Great Britain and Ireland, London, 1946).

    Google Scholar 

  24. F. Raiesi and A. Behesti, “Soil specific enzyme activity shows more clearly soil responses to paddy rice cultivation than absolute enzyme activity in primary forests of northwest Iran,” Appl. Soil Ecol. 75, 63–70 (2014). https://doi.org/10.1016/j.apsoil.2013.10.012

    Article  Google Scholar 

  25. R. Rakshit, A. Das, R. Padbhushan, R. P. Sharma, Sushant, and S. Kumar, “Assessment of soil quality and identification of parameters influencing system yield under long-term fertilizer trial,” J. Indian Soc. Soil Sci. 66, 166–171 (2018). https://doi.org/10.5958/0974-0228.2018.00021.X

    Article  Google Scholar 

  26. C. Singh, R. Rakshit, A. Das, and P. Bharti, “Interpretations of elemental and microbial phosphorus indicators to understand P availability in soils under rice–wheat cropping system,” Agric. Res. 9, 329–339 (2020). https://doi.org/10.1007/s40003-019-00439-1

    Article  CAS  Google Scholar 

  27. M. A. Tabatabai and J. M. Bremner, “Use of p-nitrophenyl phosphate for assay of soil phosphatase activity,” Soil Biol. Biochem. 1, 301–307 (1969). https://doi.org/10.1016/0038-0717(69)90012-1

    Article  CAS  Google Scholar 

  28. M. A. Tabatabai and J. M. Bremner, “Assay of urease activity in soils,” Soil Biol. Biochem. 4, 479–487 (1972). https://doi.org/10.1016/0038-0717(72)90064-8

    Article  CAS  Google Scholar 

  29. E. D. Vance, P. C. Brookes, and D. S. Jenkinson, “An extraction method for measuring soil microbial biomass C,” Soil Biol. Biochem. 19 (6), 703–707 (1987). https://doi.org/10.1016/0038-0717(87)90052-6

    Article  CAS  Google Scholar 

  30. M. P. Waldrop, T. C. Balser, and M. K. Firestone, “Linking microbial community composition to function in a tropical soil,” Soil Biol. Biochem. 32, 1837–1846 (2000). https://doi.org/10.1016/S0038-0717(00)00157-7

    Article  CAS  Google Scholar 

  31. A. J. Walkley and I. A. Black, “An examination of Degtjareff method for determining soil organic matter and a proposed modification of the chromic acid titration method,” Soil Sci. 37 (1), 29–38 (1934). https://doi.org/10.1097/00010694-193401000-00003

    Article  CAS  Google Scholar 

  32. B. Wang, S. Xue, G. B. Liu, G. H. Zhang, G. Li, and Z. P. Ren, “Changes in soil nutrient and enzyme activities under different vegetations in the Loess Plateau area, Northwest China,” Catena 92, 186–195 (2012). https://doi.org/10.1016/j.catena.2011.12.004

    Article  CAS  Google Scholar 

  33. Y. Wang, N. Hu, T. Ge, Y. Kuzyakov, Z-L. Wang, Z. Li, Z. Tang, Y. Chen, C. Wu, and Y. Lou, “Soil aggregation regulates distributions of carbon, microbial community and enzyme activities after 23-year manure amendment,” Appl. Soil Ecol. 111, 65–72 (2017). https://doi.org/10.1016/j.apsoil.2016.11.015

    Article  Google Scholar 

  34. H. Yu, W. Ding, J. Luo, R. Geng, and Z. Cai, “Long-term application of organic manure and mineral fertilizers on aggregation and aggregate-associated carbon in a sandy loam soil,” Soil Tillage Res. 124, 170–177 (2012). https://doi.org/10.1016/j.still.2012.06.011

    Article  Google Scholar 

  35. P. Bharti, A. Das, S. R. Choudhury, S. Shambhavi, P. Ganguly, B. Bihari, S. Kumar, and R. Rakshit, “Soil aggregation controls biological activities on long-term integration of organic amendments and inorganic fertilizers in rice-wheat cropping system,” Commun. Soil Sci. Plant Anal. 54 (13), 1865–1876 (2023). https://doi.org/10.1080/00103624.2023.2211103

    Article  CAS  Google Scholar 

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ACKNOWLEDGMENTS

The authors are heartily thankful to Hon’ble Vice Chancellor, Bihar Agricultural University (BAU), Sabour, Bhagalpur, India, for providing all the necessary facilities; Director of Research, BAU, Sabour for his continuous support and valuable suggestions.

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This work was supported by the Bihar Agricultural University, PG Contingency grant.

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Correspondence to Rajiv Rakshit.

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Abbreviations: SOC—soil organic carbon; MBC—microbial biomass carbon; ACP—acid phosphatase; AKP—alkaline phosphatase; DHA—dehydrogenase activity; FDA—fluorescien diacetate hydrolysing capacity; FYM—farm yard manure; WS – wheat straw; GLM—green leaf manuring.

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Bharti, P., Das, A., Kumar, S. et al. Assessment of Soil Specific Enzyme Activities in Aggregates Size Fractions: a Case Study from Subtropical Agro-ecosystem. Eurasian Soil Sc. 57, 646–656 (2024). https://doi.org/10.1134/S1064229323602627

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