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Does Rise in Temperature Adversely Affect Soil Fertility, Carbon Fractions, Microbial Biomass and Enzyme Activities under Different Land Uses?


Affiliations
1 Indian Council of Agricultural Research, Research Complex for North Eastern Hill Region, Nagaland Centre, Jharnapani, Medziphema 797 106, India
2 Indian Council of Agricultural Research, Research Complex for North Eastern Hill Region, Mizoram Centre, Kolasib 796 081, India
3 Indian Council of Agricultural Research, Research Complex for NEH Region, Umiam 793 103, India
 

We studied the variable dynamic response of different soil properties under the exposure of three elevated temperature treatments on six land-use systems. After one month of incubation, the associated changes were measured in terms of soil fertility, carbon, microbial biomass and soil enzymes. Our results confirmed the significant increase (P < 0.05) in soil available nitrogen content (by 1.85–49.32 %) with the subsequent rise in incubation temperature for soils collected from orchards and agriculture land uses. We observed a steady decrease in total organic carbon (TOC) levels with increase in incubation temperature varying between 4.1% and 31.4% (P < 0.05) across different soil types and land-use systems, resulting in a significant rising trend for microbial biomass carbon and labile carbon : TOC ratio up to 3°C elevation from maximum temperature. Among the soil enzymes, dehydrogenase, fluorescein diacetate hydrolase and β-glucosidase activity increased significantly with increase in incubation temperature from the ambient temperature, while acid phosphomonoesterase and arylsulphatase activity decreased. Our current research findings will provide new insights regarding temperature control on soil C dynamics and nutrient availability in terms of modified soil enzyme activity that will be useful to model the dynamics of soil organic matter and associated nutrient availability in acid soils.

Keywords

Carbon, Land Use, Microbial Biomass, Soil Enzyme Activity, Temperature Effects.
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  • Chatterjee, D. and Saha, S., Response of soil properties and soil microbial communities to the projected climate change. In Advances in Crop Environment Interaction (eds Bal, S. et al.) Springer, Singapore, 2018, pp. 87–136.

  • IPCC, Summary for policymakers. In Climate Change 2014: Impacts, Adaptation, and Vulnerability. Part A: Global and Sectoral Aspects. Contribution of Working Group II to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change (eds Field, C. B. et al.), Cambridge University Press, Cambridge, United Kingdom and New York, NY, USA, 2014 pp. 1–32.

  • Kumar, K. R., Kumar, K. K. and Pant, G. B., Diurnal asymmetry of surface temperature trends over India. Geophys. Res. Lett., 1994, 21, 677–680.

  • Melillo, J., Steudler, P., Aber, J., Newkirk, K., Lux, H. and Bowles, F., Soil warming and carbon-cycle feedbacks to the climate system. Science, 2002, 298, 2173–2176.

  • Stone, M. M. et al., Temperature sensitivity of soil enzyme kinetics under N-fertilization in two temperate forests. Global. Change Biol., 2012, 18, 1173–1184.

  • Steinweg, J. M., Dukes, J. S. and Wallenstein, M. D., Modeling the effects of temperature and moisture on soil enzyme activity: linking laboratory assays to continuous field data. Soil Biol. Biochem., 2012, 55, 85–92.

  • Majumder, B. et al., Organic amendments influence soil organic carbon pools and rice–wheat productivity. Soil Sci. Soc. Am. J., 2008, 72, 775.

  • Wall, G. W., McLain, J. E. T., Kimball, B. A., White, J. W., Ottman, M. J. and Garcia, R. L., Infrared warming affects intrarow soil carbon dioxide efflux during vegetative growth of spring wheat. Agron. J., 2013, 105, 607.

  • Rabbi, S. M. F. et al., The relationships between land uses, soil management practices, and soil carbon fractions in South Eastern Australia. Agric. Ecosyst. Environ., 2014, 197, 41–52.

  • Shrestha, B. M., Sitaula, B. K., Singh, B. R. and Bajracharya, R. M., Soil organic carbon stocks in soil aggregates under different land use systems in Nepal. Nutr. Cycling Agroecosyst., 2004, 70, 201–213.

  • Saha, D., Kukal, S. S. and Sharma, S., Landuse impacts on SOC fractions and aggregate stability in typic ustochrepts of Northwest India. Plant Soil, 2011, 339, 457–470.

  • Kong, X., Zhang, F., Wei, Q., Xu, Y. and Hui, J., Influence of land use change on soil nutrients in an intensive agricultural region of North China. Soil Tillage Res., 2006, 88, 85–94.

  • Zeidler, J., Hanrahan, S. and Scholes, M., Land-use intensity affects range condition in arid to semi-arid Namibia. J. Arid Environ., 2002, 52, 389–403.

  • Acosta-Martínez, V., Cruz, L., Sotomayor-Ramírez, D. and PérezAlegría, L., Enzyme activities as affected by soil properties and land use in a tropical watershed. Appl. Soil Ecol., 2007, 35, 35–45.

  • Mganga, K. Z., Razavi, B. S. and Kuzyakov, Y., Land use affects soil biochemical properties in Mt. Kilimanjaro region. CATENA, 2016, 141, 22–29.

  • Liu, X.-L. et al., Impact of land use and soil fertility on distributions of soil aggregate fractions and some nutrients. Pedosphere, 2010, 20, 666–673.

  • Hazarika, S., Soil health management in the context of climate change. In Resource Conservation Technologies in the Context of Climate Change (eds Chatterjee, D. et al.), ICAR Research Complex for NEH Region, Nagaland Centre, Medziphema, 2015, pp. 18–22.

  • Rounsevell, M. D. A. and Reay, D. S., Land use and climate change in the UK. Land Use Policy, 2009, 26, S160–S169.

  • Subbiah, B. and Asija, G., A rapid procedure for assessment of available nitrogen in soils. Curr. Sci., 1956, 25, 259–260.

  • Bray, R. H. and Kurtz, L. T., Determination of total, organic, and available forms of phosphorus in soils. Soil Sci., 1945, 59, 39– 46.

  • Murphy, J. and Riley, J. P., A modified single solution method for the determination of phosphate in natural waters. Anal. Chim. Acta, 1962, 27, 31–36.

  • Hanway, J. and Hiedal, H., Soil analysis method used in Iowa State Soil Testing Laboratory. Iowa Agric., 1952, 57, 1–31.

  • Walkley, A. and Black, I. A., An examination of the degtjareff method for determining soil organic matter, and a proposed modification of the chromic acid titration method. Soil Sci., 1934, 37, 29–38.

  • Schollenberger, C. J., A rapid approximate method for determining soil organic matter. Soil Sci., 1927, 24, 65–68.

  • Blair, G., Lefroy, R. and Lisle, L., Soil carbon fractions based on their degree of oxidation, and the development of a carbon management index for agricultural systems. Aust. J. Agric. Res., 1995, 46, 1459.

  • Witt, C., Gaunt, J. L., Galicia, C. C., Ottow, J. C. G. and Neue, H.-U., A rapid chloroform fumigation–extraction method for measuring soil microbial biomass carbon and nitrogen in flooded rice soils. Biol. Fertil. Soils, 2000, 30, 510–519.

  • Joergensen, R. G., Mueller, T. and Wolters, V., Total carbohydrates of the soil microbial biomass in 0.5 M K2SO4 soil extracts. Soil Biol. Biochem., 1996, 28, 1147–1153.

  • Casida, L. E., Klein, D. A. and Santoro, T., Soil dehydrogenase activity. Soil Sci., 1964, 98, 371–376.

  • Adam, G. and Duncan, H., Development of a sensitive and rapid method for the measurement of total microbial activity using fluorescein diacetate (FDA) in a range of soils. Soil Biol. Biochem., 2001, 33, 943–951.

  • Tabatabai, M. A., Soil enzymes. In Methods of Soil Analysis. Part 2. Chemical and Microbiological Properties (eds Page, A. L., Miller, R. H. and Keeney, D. R.), Soil Science Society of America, Madison, Wiscousin, USA, 1982, pp. 903–947.

  • Schinner, F., Kandeler, E. and Margesin, R., Methods in Soil Biology (eds Schinner, F. et al.), Springer, Berlin, Germany, 1996.

  • Eivazi, F. and Tabatabai, M. A., Glucosidases and galactosidases in soils. Soil Biol. Biochem., 1988, 20, 601–606.

  • Lukac, M., Calfapietra, C., Lagomarsino, A. and Loreto, F., Global climate change and tree nutrition: effects of elevated CO2 and temperature. Tree Physiol., 2010, 30, 1209–1220.

  • Pendall, E. et al., Below-ground process responses to elevated CO2 and temperature: a discussion of observations, measurement methods, and models. New Phytol., 2004, 162, 311–322.

  • Megan Steinweg, J., Dukes, J. S., Paul, E. A. and Wallenstein, M. D., Microbial responses to multi-factor climate change: effects on soil enzymes. Front. Microbiol., 2013, 4, 1–11.

  • Sardans, J. and Peñuelas, J., Potassium: a neglected nutrient in global change. Global Ecol. Biogeogr., 2015, 24, 261–275.

  • Zhang, Y., Chen, X., Zhang, C., Pan, G. and Zhang, X., Availability of soil nitrogen and phosphorus under elevated [CO2] and temperature in the Taihu Lake region, China. J. Plant Nutr. Soil Sci., 2014, 177, 343–348.

  • Silveira, M. L. and O’Connor, G. A., Temperature effects on phosphorus release from a biosolids-amended soil. Appl. Environ. Soil Sci., 2013, 2013.

  • Wang, X. et al., Effects of short-term and long-term warming on soil nutrients, microbial biomass and enzyme activities in an alpine meadow on the Qinghai–Tibet Plateau of China. Soil Biol. Biochem., 2014, 76, 140–142.

  • Hunsigi, G., Soil temperature and nutrient availability. Ann. Arid Zone, 1975, 14, 87–91.

  • Lal, R., Restoring soil quality to mitigate soil degradation. Sustainability, 2015, 7, 5875–5895.

  • Gama-Rodrigues, E. F., Ramachandran Nair, P. K., Nair, V. D., Gama-Rodrigues, A. C., Baligar, V. C., and Machado, R. C. R., Carbon storage in soil size fractions under two Cacao Agroforestry Systems in Bahia, Brazil. Environ. Manage., 2010, 45, 274–283.

  • Noponen, M. R. A., Healey, J. R., Soto, G. and Haggar, J. P., Sink or source – the potential of coffee agroforestry systems to sequester atmospheric CO2 into soil organic carbon. Agric. Ecosyst. Environ., 2013, 175, 60–68.

  • von Lützow, M. and Kögel-Knabner, I., Temperature sensitivity of soil organic matter decomposition – what do we know? Biol. Fertil. Soils, 2009, 46, 1–15.

  • Hartley, I. P. and Ineson, P., Substrate quality and the temperature sensitivity of soil organic matter decomposition. Soil Biol. Biochem., 2008, 40, 1567–1574.

  • Curiel Yuste, J., Ma, S. and Baldocchi, D. D., Plant–soil interactions and acclimation to temperature of microbial-mediated soil respiration may affect predictions of soil CO2 efflux. Biogeochemistry, 2010, 98, 127–138.

  • Allison, S. D., Wallenstein, M. D. and Bradford, M. A., Soilcarbon response to warming dependent on microbial physiology. Nature Geosci., 2010, 3, 336–340.

  • Joergensen, R. G., Brookes, P. C. and Jenkinson, D. S., Survival of the soil microbial biomass at elevated temperatures. Soil Biol. Biochem., 1990, 22, 1129–1136.

  • Koch, O., Tscherko, D. and Kandeler, E., Temperature sensitivity of microbial respiration, nitrogen mineralization, and potential soil enzyme activities in organic alpine soils. Global Biogeochem. Cycles, 2007, 21, GB4017.

  • Allison, S. D. and Vitousek, P. M., Responses of extracellular enzymes to simple and complex nutrient inputs. Soil Biol. Biochem., 2005, 37, 937–944.

  • Bhattacharyya, P. et al., Influence of elevated carbon dioxide and temperature on belowground carbon allocation and enzyme activities in tropical flooded soil planted with rice. Environ. Monit. Assess., 2013, 185, 8659–8671.

  • Manoj-Kumar, Swarup, A., Patra, A. K., Purakayastha, T. J., Manjaiah, K. M. and Rakshit, R., Elevated CO2 and temperature effects on phosphorus dynamics in rhizosphere of wheat (Triticum aestivum L.) grown in a typic haplustept of subtropical India. Agrochimica, 2011, 55, 314–331.

  • Das, S., Bhattacharyya, P. and Adhya, T. K., Interaction effects of elevated CO2 and temperature on microbial biomass and enzyme activities in tropical rice soils. Environ. Monit. Assess., 2011, 182, 555–569.


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  • Does Rise in Temperature Adversely Affect Soil Fertility, Carbon Fractions, Microbial Biomass and Enzyme Activities under Different Land Uses?

Abstract Views: 390  |  PDF Views: 131

Authors

Dibyendu Chatterjee
Indian Council of Agricultural Research, Research Complex for North Eastern Hill Region, Nagaland Centre, Jharnapani, Medziphema 797 106, India
Rukuosietuo Kuotsu
Indian Council of Agricultural Research, Research Complex for North Eastern Hill Region, Nagaland Centre, Jharnapani, Medziphema 797 106, India
Merasenla Ao
Indian Council of Agricultural Research, Research Complex for North Eastern Hill Region, Nagaland Centre, Jharnapani, Medziphema 797 106, India
Saurav Saha
Indian Council of Agricultural Research, Research Complex for North Eastern Hill Region, Mizoram Centre, Kolasib 796 081, India
Sanjay Kumar Ray
Indian Council of Agricultural Research, Research Complex for North Eastern Hill Region, Nagaland Centre, Jharnapani, Medziphema 797 106, India
S. V. Ngachan
Indian Council of Agricultural Research, Research Complex for NEH Region, Umiam 793 103, India

Abstract


We studied the variable dynamic response of different soil properties under the exposure of three elevated temperature treatments on six land-use systems. After one month of incubation, the associated changes were measured in terms of soil fertility, carbon, microbial biomass and soil enzymes. Our results confirmed the significant increase (P < 0.05) in soil available nitrogen content (by 1.85–49.32 %) with the subsequent rise in incubation temperature for soils collected from orchards and agriculture land uses. We observed a steady decrease in total organic carbon (TOC) levels with increase in incubation temperature varying between 4.1% and 31.4% (P < 0.05) across different soil types and land-use systems, resulting in a significant rising trend for microbial biomass carbon and labile carbon : TOC ratio up to 3°C elevation from maximum temperature. Among the soil enzymes, dehydrogenase, fluorescein diacetate hydrolase and β-glucosidase activity increased significantly with increase in incubation temperature from the ambient temperature, while acid phosphomonoesterase and arylsulphatase activity decreased. Our current research findings will provide new insights regarding temperature control on soil C dynamics and nutrient availability in terms of modified soil enzyme activity that will be useful to model the dynamics of soil organic matter and associated nutrient availability in acid soils.

Keywords


Carbon, Land Use, Microbial Biomass, Soil Enzyme Activity, Temperature Effects.

References





DOI: https://doi.org/10.18520/cs%2Fv116%2Fi12%2F2044-2054