Plant and Soil

, Volume 329, Issue 1–2, pp 227–238 | Cite as

Size, activity and catabolic diversity of the soil microbial biomass in a wetland complex invaded by reed canary grass

  • Pierre-André Jacinthe
  • Jonathan S. Bills
  • Lenore P. Tedesco
Regular Article

Abstract

Reed canary grass (Phalaris arundinacea, L.) invasion of wetlands is an ecological issue that has received attention, but its impact on soil microbial diversity is not well documented. The present study assessed the size (substrate-induced respiration), catabolic diversity (CLPP, community level physiological profiles) and composition (selective inhibition) of the soil microbial community in invaded (>95% P. arundinacea cover) and in non-invaded areas of a wetland occupied by native species grown either as a mixed assemblage (22 species) or as quasi-monotypic stands of Scirpus cyperinus (74% cover). The study also tested the hypothesis that decomposition of lignin- and phenolics-rich plant tissues would be fastest in soils exhibiting high catabolic diversity. Results showed that soil respiration, microbial biomass and diversity were significantly higher (P < 0.03; 1.5 to 3 fold) in P. arundinacea-invaded soils than in soils supporting native plant species. Fungal to bacterial ratios were also higher in invaded (0.6) than in non-invaded (0.4) plots. Further, canonical discriminant analysis of CLPP data showed distinct communities of soil decomposers associated with each plant community. However, these differences in microbial attributes had no effect on decomposition of plant biomass which was primarily controlled by its chemical composition. While P. arundinacea invasion has substantially reduced plant diversity, this study found no parallel decline in the size and diversity of the soil microbial community in the invaded areas.

Keywords

Biomass decomposition Microbial diversity Phalaris arundinacea Soil microbial biomass Wetlands 

Abbreviations

BSR

basal soil respiration

CLPP

community level physiological profiles

MBC

microbial biomass carbon

RQI

residue quality index

SOC

soil organic carbon

Notes

Acknowledgements

The authors thank the Sycamore Land Trust for providing access to the study site; Andrew Mertz, of Indy Parks, for his help with the vegetation survey; Vince Hernly and Bob Hall for their support with field reconnaissance and well installation; and several interns from the Center for Earth and Environmental Science (IUPUI) who helped with field sampling.

References

  1. Anderson JPE, Domsch KH (1975) Measurement of bacterial and fungal contributions to respiration of selected agricultural and forest soils. Can J Microbiol 21:314–322PubMedGoogle Scholar
  2. Bärlocher F, Graça MAS (2005) Total phenolics. In: Graça MAS, Barlocher F, Gessner MO (eds) Methods to study litter decomposition: a practical guide. Springer, Dordrecht, pp 97–99CrossRefGoogle Scholar
  3. Bending GD, Turner MK, Jones JE (2002) Interactions between crop residue and soil organic matter quality and the functional diversity of soil microbial communities. Soil Biol Biochem 34:1073–1082CrossRefGoogle Scholar
  4. Benizri E, Amiaud B (2005) Relationship between plants and soil microbial communities in fertilized grasslands. Soil Biol Biochem 37:2055–2064CrossRefGoogle Scholar
  5. Bills JS (2008) Invasive reed canary grass (Phalaris arundinacea) and carbon sequestration in a wetland complex. M.S. Thesis, Indiana UniversityGoogle Scholar
  6. Chantigny MH, Angers DA, Prevost D, Vezina LP, Chalifour FP (1997) Soil aggregation and fungal and bacterial biomass under annual and perennial cropping systems. Soil Sci Soc Am J 61:262–267CrossRefGoogle Scholar
  7. Degens BP (1998) Decreases in microbial functional diversity do not result in corresponding changes in decomposition under different moisture conditions. Soil Biol Biochem 30:1989–2000CrossRefGoogle Scholar
  8. Drury CF, Stone JA, Findlay WI (1991) Microbial biomass and soil structure associated with corn, grasses and legumes. Soil Sci Soc Am J 55:805–811Google Scholar
  9. Fog K (1988) The effect of added nitrogen on the rate of decomposition of organic matter. Biol Rev 63:433–462CrossRefGoogle Scholar
  10. Frey SD, Elliott ET, Paustian K (1999) Bacterial and fungal abundance and biomass in conventional and no-tillage agroecosystems along two climatic gradients. Soil Biol Biochem 31:573–585CrossRefGoogle Scholar
  11. Garland JL (1996) Analytical approaches to the characterization of samples of microbial communities using patterns of potential C source utilization. Soil Biol Biochem 28:213–221CrossRefGoogle Scholar
  12. Gessner MO (2005) Proximate lignin and cellulose. In: Graça MAS, Barlocher F, Gessner MO (eds) Methods to study litter decomposition: a practical guide. Springer, Dordrecht, Netherlands, pp 115–120CrossRefGoogle Scholar
  13. Grayston SJ, Wang SQ, Campbell CD, Edwards AC (1998) Selective influence of plant species on microbial diversity in the rhizosphere. Soil Biol Biochem 30:369–378CrossRefGoogle Scholar
  14. Heal OW, Anderson JM, Swift MJ (1997) Plant litter quality and decomposition: an historical overview. In: Cadisch G, Giller KE (eds) Driven by nature - plant litter quality and decomposition. CAB International, Wallingford, pp 3–10Google Scholar
  15. Hook PB, Olsen BE, Wraith JM (2004) Effects of the invasive forb Centaura maculosa on grassland carbon and nitrogen pools in Montana, USA. Ecosystems 7:686–694CrossRefGoogle Scholar
  16. Kaiser EA, Mueller T, Joergensen RG, Insam H, Heinemeyer O (1992) Evaluation of methods to estimate the soil microbial biomass and the relationship with soil texture and organic matter. Soil Biol Biochem 24:675–683CrossRefGoogle Scholar
  17. Kowalchuk GA, Buma DS, de Boer W, Klinkhamer PGL, van Veen JA (2002) Effects of above-ground plant species composition and diversity on the diversity of soil-borne microorganisms. Antonie van Leeuwenhoek J Microbiol 81:509–520CrossRefPubMedGoogle Scholar
  18. Lavergne S, Molofsky J (2004) Reed canary grass (Phalaris arundinacea) as a biological model in the study of plant invasions. Crit Rev Plant Sci 23:415–429CrossRefGoogle Scholar
  19. Li WH, Zhang C, Gao G, Zan Q, Yang Z (2007) Relationship between Mikania micrantha invasion and soil microbial biomass, respiration and functional diversity. Plant Soil 296:197–207CrossRefGoogle Scholar
  20. Liao C, Luo Y, Jiang L, Zhou X, Wu X, Fang C, Cheng J, Li B (2007) Invasion of Spartina alterniflora enhanced ecosystem carbon and nitrogen stocks in the Yangtze Estuary, China. Ecosystems 10:1351–1361CrossRefGoogle Scholar
  21. Lu YH, Watanabe A, Kimura M (2002) Contribution of plant-derived carbon to soil microbial biomass dynamics in a paddy rice microcosm. Biol Fert Soils 36:136–142CrossRefGoogle Scholar
  22. Marchante E, Kjoller A, Struwe S, Freitas H (2008) Invasive Acacia longifolia induce changes in the microbial catabolic diversity of sand dunes. Soil Biol Biochem 40:2563–2568CrossRefGoogle Scholar
  23. Meier CL, Bowman WD (2008) Links between plant litter chemistry, species diversity, and below-ground ecosystem function. Proc Natl Acad Sci USA 105:19780–19785CrossRefPubMedGoogle Scholar
  24. Rodriguez-Loinaz G, Onaindia M, Amezaga I, Mijangos I, Grabisu C (2008) Relationship between vegetation diversity and soil functional diversity in native mixed-oak forests. Soil Biol Biochem 40:49–60CrossRefGoogle Scholar
  25. Rothman E, Bouchard V (2007) Regulation of carbon processes by macrophyte species in a Great Lakes coastal wetland. Wetlands 27:1134–1143CrossRefGoogle Scholar
  26. Sall SN, Masse D, Ndour NYB, Chotte JL (2006) Does cropping modify the decomposition function and the diversity of the soil microbial community of tropical fallow soil? Appl Soil Ecol 31:211–219CrossRefGoogle Scholar
  27. SAS (2003) SAS System for Windows, Version 9.1. SAS Institute Inc., CaryGoogle Scholar
  28. Sinsabaugh RL, Carreiro MM, Repert DA (2002) Allocation of extracellular enzymatic activity in relation to litter composition, N deposition, and mass loss. Biogeochemistry 60:1–24CrossRefGoogle Scholar
  29. Tamura Y, Moriyama M (2001) Nonstructural carbohydrate reserves in roots and the ability of temperate perennial grasses to overwinter in early growth stages. Plant Prod Sci 4:56–61CrossRefGoogle Scholar
  30. Tian G, Brussard L, Kang BT (1995) An index for assessing the quality of plant residues and evaluating their effects on soil and crop in the (sub-) humid tropics. Appl Soil Ecol 2:25–32CrossRefGoogle Scholar
  31. Wardle DA (1998) Controls of temporal variability of the soil microbial biomass: a global-scale synthesis. Soil Biol Biochem 30:1627–1637CrossRefGoogle Scholar
  32. Wolfe BE, Klironomos JN (2005) Breaking new ground: soil communities and exotic plant invasion. Bioscience 55:477–487CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media B.V. 2009

Authors and Affiliations

  • Pierre-André Jacinthe
    • 1
  • Jonathan S. Bills
    • 1
  • Lenore P. Tedesco
    • 1
  1. 1.Department of Earth SciencesIndiana University Purdue University Indianapolis (IUPUI)IndianapolisUSA

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