Skip to main content

Advertisement

Log in

Microbial Communities and Associated Enzyme Activities in Alpine Wetlands with Increasing Altitude on the Tibetan Plateau

  • Original Research
  • Published:
Wetlands Aims and scope Submit manuscript

Abstract

Microbial communities, enzyme activities and soil physiochemical characteristics were investigated in alpine wetlands with altitude changes in the Nyainqentanglha Mountains on the Tibetan plateau. The results showed that with an increasing altitude gradient, soil physicochemical properties such as total organic carbon (TOC), total nitrogen (TN), water-soluble organic carbon (WSOC), water-soluble organic nitrogen (WSON) and pH decreased coincident with a decrease in mean annual temperature (MAT). Bacteria biomass, fungal biomass and actinobacterial biomass all decreased with an increase in altitude gradient. The ratio of Gram-positive bacteria to Gram-negative bacteria and the ratio of cyclopropyl to precursor fatty acids all indicate that the level of environmental harshness intensified with an increase in altitude. We also found that soil enzyme activities such as phenol oxidase, peroxidase, L-asparaginase, protease, urease and alkaline phosphatase all consistently decreased with an increase in altitude gradient. Additionally, the activities of peroxidase, protease and alkaline phosphatase declined, mainly due to a reduction in enzyme activities with temperature rather than the reduction of associated microbial biomass. Statistical analysis showed that both microbial biomass and enzyme activities were significantly influenced by mean annual temperature, suggesting that temperature is a key factor that affects microbial communities and soil enzyme activities in alpine wetlands on the Tibetan Plateau and indicating that climate warming may significantly impact these areas.

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
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  • Alkorta I, Aizpurua A, Riga P, Albizu I, Amezaga I, Garbisu C (2003) Soil enzyme activities as biological indicators of soil health. Reviews on Environmental Health 18:65–73

    PubMed  Google Scholar 

  • Allison SD, Jastrow JD (2006) Activities of extracellular enzymes in physically isolated fractions of restored grassland soils. Soil Biology and Biochemistry 38:3245–3256

    Article  CAS  Google Scholar 

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

    Article  CAS  Google Scholar 

  • Atlas RM, Bartha R (1997) Microbial ecology: fundamentals and applications. 4th ed. Benjamin/ Cummings Science Publishing, New york; pp: 341, 348–350

  • Bach HJ, Munch JC (2000) Identification of bacterial sources of soil peptidases. Biology and Fertility of Soils 31:219–224

    Article  CAS  Google Scholar 

  • Boerner REJ, Decker KLM, Sutherland EK (2000) Prescribed burning effects on soil enzyme activity in a southern Ohio hardwood forest: a landscape-scale analysis. Soil Biology and Biochemistry 32:899–908

    Article  CAS  Google Scholar 

  • Bolton H, Smith JL, Link SO (1993) Soil microbial biomass and activity of a disturbed and undisturbed shrub-steppe ecosystem. Soil Biology and Biochemistry 25:545–552

    Article  Google Scholar 

  • Caldwell BA (2005) Enzyme activities as a component of soil biodiversity: a review. Pedobiologia 49:637–644

    Article  CAS  Google Scholar 

  • Djukic I, Zehetner F, Mentler A, Gerzabek MH (2010) Microbial community composition and activity in different alpine vegetation zones. Soil Biology and Biochemistry 42:155–161

    Article  CAS  Google Scholar 

  • Eivazi F, Tabatabai MA (1988) Glucosidases and galactosidases in soils. Soil Biology and Biochemistry 20:601–606

    Article  CAS  Google Scholar 

  • Erwin KL (2009) Wetlands and global climate change: the role of wetland resoration in a changing world. Wetlands Ecology and Management 17:71–84

    Article  Google Scholar 

  • Faccio G, Kruus K, Saloheimo M, Thony-Meyer L (2012) Bacterial tyrosinases and their applications. Process Biochemistry 47:1749–1760

    Article  CAS  Google Scholar 

  • Federle TW, Dobbins DC, Thorntonmanning JR, Jones DD (1986) Microbial biomass, activity, and community structure in subsurface soils. Ground Water 24:365–374

    Article  CAS  Google Scholar 

  • Fenner N, Freeman C, Reynolds B (2005) Hydrological effects on the diversity of phenolic degrading bacteria in a peatland: implications fro carbon cycling. Soil Biology and Biochemistry 37:1277–1287

    Article  CAS  Google Scholar 

  • Fierer N, Jackson RB (2006) The diversity and biogeography of soil bacterial communities. Proceedings of the National Academy of Sciences of the United States of America 103:626–631

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Freeman C, Ostle NJ, Kang H (2001) An enzyme 'latch' on a global carbon store. Nature 409:149

    Article  CAS  PubMed  Google Scholar 

  • Frostegard A, Baath E, Tunlid A (1993) Shifts in the structure of soil microbial communities in limed forests as revealed by phospholipid fatty-acid analysis. Soil Biology and Biochemistry 25:723–730

    Article  Google Scholar 

  • Garcia C, Hernandez T (1997) Biological and biochemical indicators in derelict soils subject to erosion. Soil Biology and Biochemistry 29:171–177

    Article  CAS  Google Scholar 

  • Giri DD, Shukla PN, Kashyap S, Singh P, Kashyap AK, Pandey KD (2007) Variation in methanotrophic bacterial population along an altitude gradient at two slopes in tropical dry deciduous forest. Soil Biology and Biochemistry 39:2424–2426

    Article  CAS  Google Scholar 

  • Griffiths RI, Thomson BC, James P, Bell T, Bailey M, Whiteley AS (2011) The bacterial biogeography of British soils. Environmental Microbiology 13:1642–1654

    Article  PubMed  Google Scholar 

  • Guckert JB, Hood MA, White DC (1986) Phospholipid ester-linked fatty-acid profile changes during nutrient deprivation of vibrio-cholerae-increases in the trans cis ratio and proportions of cyclopropyl fatty–acids. Applied and Environmental Microbiology 52:794–801

    CAS  PubMed  PubMed Central  Google Scholar 

  • Halaouli S, Asther M, Sigoillot JC, Hamdi M, Lomascolo A (2006) Fungal tyrosinases: new prospects in molecular characteristics, bioengineering and biotechnological applications. Journal of Applied Microbiology 100:219–232

  • Jones DL, Willett VB (2006) Experimental evaluation of methods to quantify dissolved organic nitrogen (DON) and dissolved organic carbon (DOC) in soil. Soil Biology and Biochemistry 38:991–999

    Article  CAS  Google Scholar 

  • Kamimura Y, Hayano K (2000) Properties of protease extracted from tea-field soil. Biology and Fertility of Soils 30:351–355

    Article  CAS  Google Scholar 

  • Kandeler E, Gerber H (1988) Short-term assay of soil urease activity using colorimetric determination of ammonium. Biology and Fertility of Soils 6:68–72

    Article  CAS  Google Scholar 

  • Kieft TL, Wilch E, O'Connor K, Ringelberg DB, White DC (1997) Survival and phospholipid fatty acid profiles of surface and subsurface bacteria in natural sediment microcosms. Applied and Environmental Microbiology 63:1531–1542

    CAS  PubMed  PubMed Central  Google Scholar 

  • Kourtev PS, Ehrenfeld JG, Haggblom M (2002) Exotic plant species alter the microbial community structure and function in the soil. Ecology 83:3152–3166

    Article  Google Scholar 

  • Ladd J, Butler J (1972) Short–term assays of soil proteolytic enzyme activities using proteins and dipeptide derivatives as substrates. Soil Biology and Biochemistry 4:19–30

    Article  CAS  Google Scholar 

  • Limpens L, Berendse F, Blodau C, Canadell JG, Freeman C, Holden J, Roulet N, Rydin H, Schaepman-Strub G (2008) Peatlands and the carbon cycle: from local processes to global implications–a synthesis. Biogeosciences 5:1475–1491

    Article  CAS  Google Scholar 

  • Lomolino MV (2001) Elevation gradients of species-density: historical and prospective views. Global Ecology and Biogeography 10:3–13

    Article  Google Scholar 

  • Lovell RD, Jarvis SC, Bardgett RD (1995) Soil microbial biomass and activity in long–term grassland– effects of management changes. Soil Biology and Biochemistry 27:969–975

    Article  CAS  Google Scholar 

  • Ma XJ, Chen T, Zhang GS, Wang R (2004) Microbial community structure along an altitude gradient in three different localities. Folia Microbiologica 49:105–111

    Article  CAS  PubMed  Google Scholar 

  • Ma K, Zhang Y, Tang SX, Liu J (2016) Spatial distribution of soil organic carbon in the Zoige alpine wetland, northeastern Qinghai–Tibet plateau. Catena 144:102–108

    Article  CAS  Google Scholar 

  • Mannisto MK, Tiirola M, Haggblom MM (2007) Bacterial communities in Arctic fjelds of Finnish Lapland are stable but highly pH–dependent. FEMS Microbiology Ecology 59:452–465

    Article  CAS  PubMed  Google Scholar 

  • Margesin R, Gander S, Zacke G, Gounot AM, Schinner F (2003) Hydrocarbon degradation and enzyme activities of cold-adapted bacteria and yeasts. Extremophiles 7(6):451–458

  • Margesin R, Jud M, Tscherko D, Schinner F (2009) Microbial communities and activities in alpine and subalpine soils. FEMS Microbiology Ecology 67:208–218

    Article  CAS  PubMed  Google Scholar 

  • Mayer AM (2006) Polyphenol oxidases in plants and fungi: going places? A review. Phytochemistry 67:2318–2331

    Article  CAS  PubMed  Google Scholar 

  • Mutabaruka R, Hairiah K, Cadisch G (2007) Microbial degradation of hydrolysable and condensed tannin polyphenol-protein complexes in soils from different land-use histories. Soil Biology and Biochemistry 39:1479–1492

    Article  CAS  Google Scholar 

  • Qing Q, Yang B, Wyman CE (2010) Xylooligomers are strong inhibitors of cellulose hydrolysis by enzymes. Bioresource Technology 101:9624–9630

    Article  CAS  PubMed  Google Scholar 

  • Rahbek C (2005) The role of spatial scale and the perception of large-scale species-richness patterns. Ecology Letters 8:224–239

    Article  Google Scholar 

  • Rousk J, Baath E, Brookes PC, Lauber CL, Lozupone C, Caporaso JG, Knight R, Fierer N (2010) Soil bacterial and fungal communities across a pH gradient in an arable soil. The ISME Journal 4:1340–1351

    Article  PubMed  Google Scholar 

  • Schinner F, Gstraunthaler G (1981) Adaptation of microbial activities to the environmental-conditions in alpine soils. Oecologia 50:113–116

    Article  PubMed  Google Scholar 

  • Shen C, Xiong J, Zhang H, Feng Y, Lin X, Li X, Liang W, Chu H (2013) Soil pH drives the spatial distribution of bacterial communities along elevation on Changbai Mountain. Soil Biology and Biochemistry 57:204–211

    Article  CAS  Google Scholar 

  • Sinsabaugh RL, Carreiro MM, Repert DA (2002) Allocation of extracellular enzymatic activity in relation to litter composition, N deposition, and mass loss. Biogeochemistry 60:1–24

    Article  CAS  Google Scholar 

  • Tscherko D, Rustemeier J, Richter A, Wanek W, Kandeler E (2003) Functional diversity of the soil microflora in primary succession across two glacier forelands in the central alps. European Journal of Soil Science 54:685–696

    Article  Google Scholar 

  • Tunlid A, Hoitink HAJ, Low C, White DC (1989) Characterization of bacteria that suppress rhizoctonia damping–off in bark compost media by analysis of fatty–acid biomarkers. Applied and Environmental Microbiology 55:1368–1374

    CAS  PubMed  PubMed Central  Google Scholar 

  • Uchima CA, Tokuda G, Watanabe H, Kitamoto K, Arioka M (2011) Heterologous expression and characterization of a glucose-stimulated β-glucosidase from the termite Neotermes Koshunensis in aspergillus oryzae. Applied Microbiology and Biotechnology 89:1761–1771

    Article  CAS  PubMed  Google Scholar 

  • Wagai R, Kitayama K, Satomura T, Fujinuma R, Balser T (2011) Interactive influences of climate and parent material on soil microbial community structure in Bornean tropical forest ecosystems. Ecological Research 26:627–636

    Article  Google Scholar 

  • Waldrop MP, Balser TC, Firestone MK (2000) Linking microbial community composition to function in a tropical soil. Soil Biology and Biochemistry 32:1837–1846

    Article  CAS  Google Scholar 

  • Wang Z, Luo T, Li R, Tang Y, Du M (2013) Causes for the unimodal pattern of biomass and productivity in alpine grasslands along a large altitudinal gradient in semi–arid regions. Journal of Vegetation Science 24:189–201

    Article  Google Scholar 

  • White D, Davis W, Nickels J, King J, Bobbie R (1979) Determination of the sedimentary microbial biomass by extractible lipid phosphate. Oecologia 40:51–62

    Article  CAS  PubMed  Google Scholar 

  • Yao TD, Liu XD, Wang NL, Shi YF (2000) Amplitude of climatic changes in Qinghai–Tibetan plateau. Chinese Science Bulletin 45:1236–1243

    Article  Google Scholar 

  • Zelles L (1997) Phospholipid fatty acid profiles in selected members of soil microbial communities. Chemosphere 35:275–294

    Article  CAS  PubMed  Google Scholar 

  • Zogg GP, Zak DR, Ringelberg DB, MacDonald NW, Pregitzer KS, White DC (1997) Compositional and functional shifts in microbial communities due to soil warming. Soil Science Society of America Journal 61:475–481

    Article  CAS  Google Scholar 

Download references

Acknowledgements

This work was funded by 973 Project from Science & Technology Department of China (2010CB951304–3), the Knowledge Innovation Program of the Chinese Academy of Sciences (KZCX2–EW–112), and the Program of western light of the Chinese Academy of Sciences (Y508RC1SGC).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Zhang Gengxin.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Tianzhu, L., Guicai, S., Jian, W. et al. Microbial Communities and Associated Enzyme Activities in Alpine Wetlands with Increasing Altitude on the Tibetan Plateau. Wetlands 37, 401–412 (2017). https://doi.org/10.1007/s13157-017-0876-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13157-017-0876-6

Keywords

Navigation