Exogenous application of EE-GRSP and changes in citrus rhizosphere properties


Abstract views: 209 / PDF downloads: 27

Authors

  • QIANG-SHENG WU Professor, College of Horticulture and Gardening/Institute of Root Biology, Yangtze University, Jingzhou, Hubei 434 025, China
  • A K SRIVASTAVA Principal Scientist, Soil Science, Central Citrus Research Institute, Nagpur, Maharashtra 440 010
  • SHUANG WANG College of Horticulture and Gardening/Institute of Root Biology, Yangtze University, Jingzhou, Hubei 434025, China
  • JIA-XIN ZENG College of Horticulture and Gardening/Institute of Root Biology, Yangtze University, Jingzhou, Hubei 434025, China

https://doi.org/10.56093/ijas.v85i6.49233

Keywords:

Aggregate stability, Carbon, Glomalin, Water-stable aggregate

Abstract

Mycorrhization-induced secretion of glomalin-related soil protein (GRSP) is known to contribute in improving soil fertility and aggregate stability. But, there is hardly any evidence that exogenous GRSP could produce the similar type of response. The present study was, therefore, carried out to extract easily extractable GRSP (EE-GRSP) from citrus rhizosphere soils and evaluate the response at 1/4, 1/2 and full strength EE-GRSP solutions watered into the rhizosphere of 27-year-old Satsuma mandarin (Citrus unshiu) grafted on the rootstock of Poncirus trifoliata. After ~5 months, exogenous EE-GRSP treatments produced significantly positive responses on endogenous EE-GRSP, difficultly-extractable GRSP (DE-GRSP), total GRSP production and soil organic carbon (SOC) content. A significantly positive correlation of these endogenous GRSP fractions with SOC indicated an active participation of GRSP on soil C pool. Exogenous GRSP showed a key role in binding water-stable aggregate (WSA) at 2–4, 1–2, 0.5–1, and 0.25– 0.5 mm size and enhancing WSA stability through changes in mean weight diameter (MWD). A stronger correlation of EE-GRSP and total GRSP with MWD was observed than DE-GRSP fraction. On the other hand, exogenous EEGRSP showed a positive effect on soil phosphatase activity, and soil endogenous EE-GRSP was significantly and positively correlated only with neutral phosphatase. Our studies suggest that exogenous EE-GRSP could be used as an effective regulator to affect soil fertility and soil structure within citrus rhizosphere.

Downloads

Download data is not yet available.

References

Borie F, Rubio R, Morales A, Curaqueo G and Cornejo P. 2010. Arbuscular mycorrhizae in agricultural and forest ecosystems in Chile. Journal of Soil Science and Plant Nutrition 10: 185– 206. DOI: https://doi.org/10.4067/S0718-95162010000100001

Bradford M M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry 72: 248–54. DOI: https://doi.org/10.1016/0003-2697(76)90527-3

Eyheraguibel B, Silvestre J and Morard P. 2008. Effects of humic substances derived from organic waste enhancement on the growth and mineral nutrition of maize. Bioresource Technology 99: 4 206–12. DOI: https://doi.org/10.1016/j.biortech.2007.08.082

Fokom R, Teugwa Mofor C, Nana Wakam L, Ngonkeu Megapche E L, Tchameni S, Nwage D, Rillig M C and Amvam Zollo P H. 2013. Glomalin, carbon, nitrogen and soil aggregate stability as affected by land use changes in the humid forest zone in south Cameroon. Applied Ecology and Environmental Research 11: 581–92. DOI: https://doi.org/10.15666/aeer/1104_581592

Fokom R, Adamou S, Teugwa M C, Begoude Boyogueno A D, Nana W L, Ngonkeu M E L, Tchameni N S, Nwaga D, Tsala Ndzomo G and Amvam Zollo P H. 2012. Glomalin related soil protein, carbon, nitrogen and soil aggregate stability as affected by land use variation in the humid forest zone of south Cameroon. Soil Tillage Research 120: 69–75. DOI: https://doi.org/10.1016/j.still.2011.11.004

Gispert M, Emran M, Pardini G, Doni S and Ceccanti B. 2013. The impact of land management and abandonment on soil enzymatic activity, glomalin content and aggregate stability. Geoderma 202-203: 51–61. DOI: https://doi.org/10.1016/j.geoderma.2013.03.012

Kemper W and Rosenau R. 1986. Aggregate stability and size distribution, pp 425–442. (In) Methods of Soil Analysis: Part 1. Physical and Mineralogical Methods. Klute A (Ed). Agronomy Monograph. American Society of Agronomy and Soil Science Society of America, US. DOI: https://doi.org/10.2136/sssabookser5.1.2ed.c17

Koide R T and Peoples M S. 2013. Behavior of Bradford-reactive substances is consistent with predictions for glomalin. Applied Soil Ecology 63: 8–14. DOI: https://doi.org/10.1016/j.apsoil.2012.09.015

Peng S L, Guo T and Liu G C. 2013. The effects of arbuscular mycorrhizal hyphal networks on soil aggregations of purple soil in southwest China. Soil Biology and Biochemistry 57: 411–7. DOI: https://doi.org/10.1016/j.soilbio.2012.10.026

Rillig M C, Wright S F, Nichols K A, Schmidt W F and Torn M S. 2001. Large contribution of arbuscular mycorrhizal fungi to soil carbon pools in tropical forest soils. Plant and Soil 233: 167–77. DOI: https://doi.org/10.1023/A:1010364221169

Rillig M C, Ramsey P W, Morris S and Paul E A. 2003. Glomalin, an arbuscular-mycorrhizal fungal soil protein, responds to landuse change. Plant and Soil 253: 293–9. DOI: https://doi.org/10.1023/A:1024807820579

Rillig M C. 2004. Arbuscular mycorrhizae, glomalin, and soil aggregation. Canadian Journal of Soil Science 84: 355–63. DOI: https://doi.org/10.4141/S04-003

Rowell D L. 1994. Soil Science: Methods and Applications. Longman Group UK Ltd, London.

Treseder K K and Turner K M. 2007. Glomalin in ecosystems. Soil Science Society of Americal Journal 71: 1 257–66. DOI: https://doi.org/10.2136/sssaj2006.0377

Walley F L, Gillespie A W, Adetona A B, Germida J J and Farrell R E. 2014. Manipulation of rhizosphere organisms to enhance glomalin production and C-sequestration: Pitfalls and promises. Canadian Journal of Plant Science 94: 1 025–32. DOI: https://doi.org/10.4141/cjps2013-146

Wang S, Srivastava A K, Wu Q S and Fokom R. 2014.The effect of mycorrhizal inoculation on the rhizosphere properties of trifoliate orange (Poncirus trifoliata L. Raf.). Scientia Horticulturae 170: 137–42. DOI: https://doi.org/10.1016/j.scienta.2014.03.003

Wright S F and Upadhyaya A. 1998. A survey of soils for aggregate stability and glomalin, a glycoprotein produced by hyphae of arbuscular mycorrhizal fungi. Plant and Soil 198: 97–107.

Wu Q S, He X H, Zou Y N, He K P, Sun Y H and Cao M Q. 2012. Spatial distribution of glomalin-related soil protein and its relationships with root mycorrhization, soil aggregates, carbohydrates, activity of protease and -glucosidase in the rhizosphere of Citrus unshiu. Soil Biology and Biochemistry 45: 181–3. DOI: https://doi.org/10.1016/j.soilbio.2011.10.002

Wu Q S, Cao M Q, Zou Y N and He X H. 2014. Direct and indirect effects of glomalin, mycorrhizal hyphae, and roots on aggregate stability in rhizosphere of trifoliate orange. Scientific Reports 4: 5 823 DOI: 10.1038/srep05823. DOI: https://doi.org/10.1038/srep05823

Wu Q S, Xia R X and Zou Y N. 2008. Improved soil structure and citrus growth after inoculation with three arbuscular mycorrhizal fungi under drought stress. European Journal of Soil Biology 44: 122–8. DOI: https://doi.org/10.1016/j.ejsobi.2007.10.001

Zhao L P and Jiang Y. 1986. Determination of soil phosphatase activity. Chinese Journal of Soil Science 17: 138–41 (in Chinese).

Downloads

Submitted

2015-06-08

Published

2015-06-08

Issue

Section

Articles

How to Cite

WU, Q.-S., SRIVASTAVA, A. K., WANG, S., & ZENG, J.-X. (2015). Exogenous application of EE-GRSP and changes in citrus rhizosphere properties. The Indian Journal of Agricultural Sciences, 85(6), 802-806. https://doi.org/10.56093/ijas.v85i6.49233
Citation