Skip to main content

Advertisement

Log in

Nutrient cycling and metabolic activity of soil microbes in pristine forests in comparison to a monoculture

  • Research Articles
  • Published:
Vegetos Aims and scope Submit manuscript

Abstract

Soil health in terms of nutrient cycling, metabolic activities and microbial diversity is measured and compared among four different forests in Gangajalghati forest area of Bankura district, West Bengal, India. Three of these forests are of pristine nature and one is Eucalyptus monoculture. The microbial diversity in terms of species richness is considerably higher in pristine forests as compared to the Eucalyptus monoculture. The P values determined using statistical tools like Wilcoxon rank sum test and Kolmogrov Smirnov test reveal significant difference in carbon and nitrogen contents and also in acid phosphatase activity between the pristine forests and the man-made monoculture forest. The elemental analysis through EDX also suggests a better nutrient cycling owing to greater microbial activity in the pristine forests than its monoculture counterpart. It also revealed a higher concentration of some heavy metals viz., Cd, Pb and Cr in the monoculture type forest. However, phosphorus content, basal respiration and dehydrogenase (DHA) activities remains to be the same in these characteristically two types of forests. Most of the parameters indicate a poor nutrient shuffling and microbial diversity in the man-made monoculture of Eucalyptus and a reforestation practice of this kind is not encouraging.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  • Amador JA, Glucksman AM, Lyons JB, Gorres JH (1997) Spatial distribution of soil phosphatase activity within a riparian forest. Soil Sci 162:808–825

    Article  CAS  Google Scholar 

  • Anderson JPE, Domsch H (1973) Quantification of bacterial and fungal contributions to soil respiration. Arch Mikrobiol 93:113–127

    Article  CAS  Google Scholar 

  • Bandick AK, Dick RP (1999) Field management effects on soil enzyme activities. Soil Biol Biochem 31:1471–1479

    Article  CAS  Google Scholar 

  • Barjora Gangajalghati Planning Authority (1979) Dist. Bankura: West Bengal. Modified by WBT and C (P and D) Act

  • Black CA (1965) Methods of soil analyses. Agronomy. Amer Soc. Agron Madison, Wisconsin, USA, p 9

  • Burns RG (1982) Enzyme activity in soil: location and a possible role in microbial ecology. Soil Biol Biochem 1982(14):423–427

    Article  Google Scholar 

  • Burylo M, Rey F, Delcros P (2007) Abiotic and biotic factors influencing the early stages of vegetation colonization in restored marly gullies (Southern Alps, France). Ecol Eng 30(3):231–239

    Article  Google Scholar 

  • Chatterjee S, Bhaduri A, Raha S, Bakuli K, Pandey S (2018) Floral composition and soil properties of prestine forests in comparison to managed forests in Gangajalghatiforest area of West Bengal. India. Int J Sci Res Rev 7(1):159–178

    Google Scholar 

  • Chen TH, Chiu CY, Tian GL (2005) Seasonal dynamics of soil microbial biomass in coastal sand dune forest. Pedobiologia 49:645–653

    Article  CAS  Google Scholar 

  • Das SK, Varma F (2011) Role of enzymes in maintaining soil health. In: Shukla G, Varma A (eds) Soil Enzymology. Springer, Berlin, pp 25–42

    Google Scholar 

  • De Deyn GB, Cornelissen JHC, Bardgett RD (2008) Plant functional traits and soil carbon sequestration in contrasting biomes. Ecol Lett 11:516–531

    Article  PubMed  Google Scholar 

  • Delgado-Baquerizo M, Maestre FT, Reich PB, Jeffries TC, Gaitan JJ, Encinar D, Berdugo M, Campbell CD, Singh BK (2016) Microbial diversity drives multifunctionality in terrestrial ecosystems. Nature Commun 7:10541. https://doi.org/10.1038/ncomms10541 (p 1–8)

    Article  CAS  Google Scholar 

  • Dick RP (1997) Soil enzyme activities as integrative indicators of soil health. In: Pankhurst CE, Doube BM, Gupta VVSR (eds) Biological indicators of soil health. CAB International, Wallingford, pp 121–156

    Google Scholar 

  • Feng WT, Zou XM, Schaefer D (2009) Above- and belowground carbon inputs affect seasonal variations of soil microbial biomass in a subtropical monsoon forest of southwest China. Soil Biol Biochem 41:978–983

    Article  CAS  Google Scholar 

  • Fisk MC, Fahey TJ (2001) Microbial biomass and nitrogen cycling responses to fertilization and litter removal in young northern hardwood forests. Biogeochemistry 53:201–223

    Article  CAS  Google Scholar 

  • Gulick A (1914) A simplification of the determination of total nitrogen by colorimetry. J Biol Chem 1914(18):541–547

    Google Scholar 

  • Haynes RJ, Swift RS (1988) Effect of lime and phosphate additions on changes in enzyme activities, microbial biomass and levels of extractable nitrogen, sulphur and phosphorus in acid soil. Biol Fertil Soils 6:153–158

    Article  CAS  Google Scholar 

  • Heanes DL (2008) Determination of total organic C in solid by an improved chromic acid digestion and spectrophotometric procedure. Commun Soil Sci Plant Anal 15:10 (1984—Issue)

    Google Scholar 

  • Jassey VE, Chiapusio G, Binet P, Buttler A (2013) Above- and below ground linkages in Sphagnum peat land: climate warming affects plant- microbial interactions. Global Chang Biol 19:811–823

    Article  Google Scholar 

  • Jin H, Sun OJ, Liu J (2010) Changes in soil microbial biomass and community structure with addition of contrasting types of plant litter in a semiarid grassland ecosystem. J Plant Ecol 3(3):209–217

    Article  Google Scholar 

  • Jordan D, Kremer RJ, Bergfield WA, Kim KY, Cacnio VN (1995) Evaluation of microbial methods as potential indicators of soil quality in historical agricultural fields. Biol Fertil Soils 19:297–302

    Article  Google Scholar 

  • Juma NG, Tabatabai MA (1978) Distribution of phosphomonoesterases in soils. Soil Sci 126:101–108

    Article  CAS  Google Scholar 

  • King EJ, Jegatheesan KA (1959) A method for the determination of tartarate labile prostratic acid phosphatase in serum. J Clin 12:85

    CAS  Google Scholar 

  • Nannipieri P, Giagnoni L, Renella G, Puglisi E, Ceccanti B, Masciandaro G, Fornasier F, Moscatelli MC, Marinari S (2012) Soil enzymology: classical and molecular approaches. Biol Fert Soil 48:743–762

    Article  Google Scholar 

  • Olsen SR, Cole CV, Watanabe FS, Dean LA (1954) Estimation of available phosphorus in soils by extraction with sodium bicarbonate. US Department of Agriculture Circular No. 939. Banderis AD, Barter DH and Anderson K. Agricultural and Advisor

  • Pascual JA, Moreno JL, Hernández T, García C (2002) Persistence of immobilized and total urease and phosphatase activities in a soil amended with organic wastes. Biores Tech 82:73–78

    Article  CAS  Google Scholar 

  • Santoja M, Rancon A, Fromin N, Baldy V (2019) Plant litter diversity increases microbial abundance, fungal diversity and carbon and nitrogen cycling in Mediterranean shrubland. Soil Biol Biochem 111:124–134

    Article  CAS  Google Scholar 

  • Schoenholtz SH, Van Miegroet H, Burger JA (2000) A review of chemical and physical properties as indicators of forest soil quality: challenges and opportunities. Forest Ecol Manag 138:335–356

    Article  Google Scholar 

  • Shapiro SS, Wilk MB (1965) An analysis of variance test for normality (complete samples). Biometrika 52(3–4):591–611

    Article  Google Scholar 

  • Speir TW, Ross DJ (1978) Soil phosphatase and sulphatase. In: Burns RG (ed) Soil enzymes. Academic Press, London, pp 198–250

    Google Scholar 

  • Thalmann A (1966) The determination of the dehydrogenase activity in soil by means of TTC (triphenyltetrazolium chloride). Soil Biol 6:46–49

    Google Scholar 

  • Trevors JT (1984) Dehydrogenase activity in soil: a comparison between the INT and TTC assay. Soil Biol Biochem 16:673–674

    Article  CAS  Google Scholar 

  • Van der Heijden MGA, Bardgett RD, van Straalen NM (2008) The unseen majority: soil microbes as drivers of plant diversity and productivity in terrestrial ecosystems. Ecol Lett 11:296–310

    Article  PubMed  Google Scholar 

  • Wang X, Zhou G, Jiang Y, Jia B, Wang F, Zhou L (2007) Soil respiration in natural mixed (Betula platyphylla and Populus davidiana) secondary forest and primary broad-leaved Korean pine forest. J Plant Ecol 31:348–354

    Article  CAS  Google Scholar 

  • Wang H, Shirong L, Chang SX, Wang J, Shi Z, Huang X, Wen Y, Liu L, Cai D (2015) Soil microbial community composition rather than litter quality is linked with soil organic carbon chemical composition in plantations in subtropical China. J Soils Sediments 15:1094–1103

    Article  CAS  Google Scholar 

  • Wardle DA, Jonsson M, Bansal S, Bardgett RD, Gundale MJ, Metcalfe DB (2012) Linking vegetation change, carbon sequestration and biodiversity: in sights from island ecosystems in a long-term natural experiment. J Ecol 100:16–30

    Article  Google Scholar 

  • Wilcoxon F (1945) Individual comparisons by ranking methods. Biometrics Bull 1(6):80–83

    Article  Google Scholar 

  • Yakovchenko V, Sikora LJ, Kaufman DD (1996) A biologically based indicator of soil quality. Biol Fertil Soils 21:245–251

    Article  Google Scholar 

  • You Y, Wang J, Huang X, Tang Z, Liu S, Sun OJ (2014) Relating microbial community structure to functioning in forest soil organic carbon transformation and turnover. Ecol Evol 4:633–647

    Article  PubMed  PubMed Central  Google Scholar 

  • Zhang PC, Tang YH, Hirota M, Yamamoto A, Mariko S (2009) Use of a regression method to partition sources of ecosystem respiration in an alpine meadow. Soil Biol Biochem 41:663–670

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We are thankful to West Bengal Department of Science and Technology for supporting this research work financially. We extend our utmost thanks to the B. B. College, Principal and Governing Body for providing me space and other facilities for lab based work related to this project. We also extend our thanks to Bankura District (North) Division Forest Department and Gangajalghati police for assisting us on our forest visits.

Funding

This work was supported by the Department of Science and Technology, Government of West Bengal (Grant no. 1G-1/2016), Department of Science and Technology, Government of West Bengal (Grant no. 105(Sanc.)/ST/P/S&T/1G-1/2016).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Sanjeev Pandey.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Bhaduri, A., Chatterjee, S., Bakuli, K. et al. Nutrient cycling and metabolic activity of soil microbes in pristine forests in comparison to a monoculture. Vegetos 32, 324–332 (2019). https://doi.org/10.1007/s42535-019-00050-3

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s42535-019-00050-3

Keywords

Navigation