Skip to main content
Log in

Physiological Profiling of Soil Microbial Communities in a Florida Scrub-Oak Ecosystem: Spatial Distribution and Nutrient Limitations

  • Original Article
  • Published:
Microbial Ecology Aims and scope Submit manuscript

Abstract

Rapid physiological profiling of heterotrophic microbial communities enables intensive analysis of the factors affecting activity in aerobic habitats, such as soil. Previous methods for performing such profiling were severely limited due to enrichment bias and inflexibility in incubation conditions. We tested a new physiological profiling approach based on a microtiter plate oxygen sensor system (Becton Dickinson Oxygen Biosensor System (BDOBS)), which allows for testing of lower substrate addition (i.e., lower enrichment potential) and manipulation of physiochemical assay conditions, such as pH and nutrients. Soil microbial communities associated with a scrub-oak forest ecosystem on Merritt Island Wildlife Refuge in central Florida, USA, were studied in order to evaluate microbial activity in a nutrient poor soil and to provide baseline data on the site for subsequent evaluation of the effects of elevated CO2 on ecosystem function. The spatial variation in physiological activity amongst different habitats (litter, bulk soil, and rhizosphere) was examined as a function of adaptation to local resources (i.e., water soluble extracts of roots and leaf litter) and the degree of N and P limitation. All the communities were primarily N-limited, with a secondary P limitation, which was greater in the rhizosphere and bulk soil. The litter community showed greater overall oxygen consumption when exposed to litter extracts relative to the rhizosphere or soil, suggesting acclimation toward greater use of the mixed substrates in the extract. Root extracts were readily used by communities from all the habitats with no habitat specific acclimation observed. A priming effect was detected in all habitats; addition of glucose caused a significant increase in the use of soil organic carbon. Response to added glucose was only observed with N and P addition, suggesting that C may be lost to the groundwater from these porous soils because nutrient limitation prevents C immobilization.

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.

Figure 1
Figure 2
Figure 3
Figure 4
Figure 5
Figure 6
Figure 7
Figure 8
Figure 9

Similar content being viewed by others

References

  1. Allen AS, Schlesinger WH (2004) Nutrient limitations to soil microbial biomass and activity in loblolly pine forests. Soil Biol Biochem 36:581–589

    Article  CAS  Google Scholar 

  2. Atlas RM (1995) Handbook of media for environmental microbiology. CRC, Boca Raton, p 277

    Google Scholar 

  3. Berg MP, Kniese JP, Verhoef HA (1998) Dynamics and stratification of bacteria and fungi in the organic layers of a Scots pine forest soil. Biol Fertil Soils 26:313–322

    Article  Google Scholar 

  4. Brown ALP (2006) Effects of elevated atmospheric CO2 on scrub-oak root carbon pools and soil microbial processes. Dissertation. Old Dominion University, Norfolk, VA

  5. Brown ALP, Day FP, Hungate BA, Drake BG, Hinkle CR (2007) Root biomass and nutrient dynamics in a scrub-oak ecosystem under the influence of elevated atmospheric CO2. Plant Soil 292:219–232

    Article  CAS  Google Scholar 

  6. Butler JL, Williams MA, Bottomley PJ, Myrold DD (2003) Microbial community dynamics associated with rhizosphere carbon flow. Appl Environ Microbiol 69:6793–6800

    Article  PubMed  CAS  Google Scholar 

  7. Canadell JG, Pitelka LF, Ingram JSI (1996) The effects of elevated (CO2) on plant-soil carbon below-ground: a summary and synthesis. Plant Soil 187:391–400

    Article  CAS  Google Scholar 

  8. Drenovsky RE, Vo D, Graham KJ, Scow KM (2004) Soil water content and organic carbon availability are major determinants of soil microbial community composition. Microb Ecol 48:424–430

    Article  PubMed  CAS  Google Scholar 

  9. Fierer N, Schimel JP, Holden PA (2003) Variations in microbial community composition through two soil depth profiles. Soil Biol Biochem 35:167–176

    Article  CAS  Google Scholar 

  10. Garland JL, Campbell CD, Mills AL (2007) Physiological profiling of microbial communities. In: Hurst CJ, Crawford RL, Garland JL, Lipson DA, Mills AL, Stetzenbach LD (eds) ASM manual of environmental microbiology. ASM, Washington, DC, pp 126–138

    Google Scholar 

  11. Garland JL, Roberts MS, Levine LF, Mills AL (2003) Community-level physiological profiling performed with an oxygen-sensitive flourophore in a microtiter plate. Appl Environ Microbiol 69:2994–2998

    Article  PubMed  CAS  Google Scholar 

  12. Goberna M, Insam H, Klammer S, Pascual JA, Sánchez J (2005) Microbial community structure at different depths in disturbed and undisturbed semiarid Mediterranean forest soils. Microb Ecol 50:315–326

    Article  PubMed  CAS  Google Scholar 

  13. Griffiths RI, Whiteley AS, O’Donnell AG, Bailey MJ (2003) Influence of depth and sampling time on bacterial community structure in an upland grassland soil. FEMS Microbiol Ecol 43:35–43

    Article  CAS  Google Scholar 

  14. Jonasson S, Michelsen A, Schmidt IK, Nielsen EV, Callaghan TV (1996) Microbial biomass C, N and P in two arctic soils and responses to addition of NPK fertilizer and sugar: implications for plant nutrient uptake. Oecologia 106:507–515

    Article  Google Scholar 

  15. Kurzatkowski D, Martius C, Höfer H, Garcia M, Förster B, Beck L, Vlek P (2004) Litter decomposition, microbial biomass and activity of soil organisms in three agroforestry sites in central Amazonia. Nutr Cycl Agroecosyst 69:257–267

    Article  CAS  Google Scholar 

  16. Kuzyakov Y, Friedel JK, Stahr K (2000) Review of mechanisms and quantification of priming effects. Soil Biol Biochem 32:1485–1498

    Article  CAS  Google Scholar 

  17. Mulvania M (1931) Ecological survey of Florida scrub. Ecology 7:528–540

    Article  Google Scholar 

  18. Paterson E, Hall JM, Rattray EAS, Griffiths BS, Ritz K, Killham K (1997) Effects of elevated CO2 on rhizosphere carbon flow and soil microbial processes. Glob Chang Biol 3:363–377

    Article  Google Scholar 

  19. Pietikäinen J, Vaijävi E, Ilvesniemi H, Fritze H, Westman CJ (1999) Carbon storage of microbes and roots and the flux of CO2 across a moisture gradient. Can J For Res 29:1197–1203

    Article  Google Scholar 

  20. Schlesinger W (1997) Biogeochemistry: an analysis of global change, 2nd edn. Academic, London

    Google Scholar 

  21. Schmalzer PA, Hinkle CR (1990) Geology, geohydrology and soils of Kennedy Space Center: A review. NASA Technical Memorandum 103813, NASA, Kennedy Space Center, Florida

    Google Scholar 

  22. Schmalzer PA, Hinkle CR (1991) Dynamics of vegetation and soils of oak/saw palmetto scrub after fire: Observations from permanent transects. NASA Technical Memorandum 103817, NASA, Kennedy Space Center, Florida

    Google Scholar 

  23. Schortemeyer M, Dijkstra P, Johnson DW, Drake BG (2000) Effects of elevated atmospheric CO2 concentration on C and N pools and rhizosphere processes in a Florida scrub oak community. Glob Chang Biol 6:383–391

    Article  Google Scholar 

  24. Steer J, Harris JA (2000) Shifts in the microbial community in rhizosphere and non-rhizosphere soils during the growth of Agrostis stolonifera. Soil Biol Biochem 32:869–878

    Article  CAS  Google Scholar 

  25. Taiz L, Zeiger E (eds) (1998) Mineral nutrition in plant physiology. Plant physiology. Sinauer, Sunderland, MA, pp 103–114

  26. Väisänen RK, Roberts MS, Garland JL, Frey SD, Dawson LA (2005) Physiological and molecular characterization of microbial communities associated with different water stable aggregate size classes. Soil Biol Biochem 37:2007–2016

    Article  Google Scholar 

  27. Vance ED, Chapin FS III (2001) Substrate limitations to microbial activity in taiga forest floors. Soil Biol Biochem 33:173–188

    Article  CAS  Google Scholar 

  28. Zabaloy MC, Lehman RM, Frey SD, Garland JL (2008) Optimization of an oxygen-based approach for community-level physiological profiling of soils. Soil Biol Biochem (in press)

Download references

Acknowledgments

We thank Dayanand Naik for statistical advice, Victoria Albarracin, Mike Roberts, Mary Hummerick, Jan Bauer, and Lanfang Levine for laboratory assistance, and the two anonymous reviewers for their time and advice. We would like to thank the National Aeronautics and Space Administration at Kennedy Space Center (KSC) and the Department of Interior U.S. Fish and Wildlife Service at Merritt Island National Wildlife Refuge for their support and cooperation in conducting this research at KSC. This research was funded by a subcontract (95-59-MPOOO02) to the Smithsonian Institution’s grant from the U.S. Department of Energy (DE-FG-02-95ER61993), by grants from the National Science Foundation Division of Environmental Biology (DEB-0445324, and DEB-0092642) and by the NASA Planetary Biology Internship Program.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Alisha L. P. Brown.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Brown, A.L.P., Garland, J.L. & Day, F.P. Physiological Profiling of Soil Microbial Communities in a Florida Scrub-Oak Ecosystem: Spatial Distribution and Nutrient Limitations. Microb Ecol 57, 14–24 (2009). https://doi.org/10.1007/s00248-008-9461-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00248-008-9461-0

Keywords

Navigation