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5 - Theory, community assembly, diversity and evolution in the microbial world

Published online by Cambridge University Press:  05 June 2012

Thomas P. Curtis
Affiliation:
School of Civil Engineering and Geosciences, University of Newcastle upon Tyne
Nigel C. Wallbridge
Affiliation:
Nomad Digital Limited
William T. Sloan
Affiliation:
Department of Civil Engineering, University of Glasgow
Roger Butlin
Affiliation:
University of Sheffield
Jon Bridle
Affiliation:
University of Bristol
Dolph Schluter
Affiliation:
University of British Columbia, Vancouver
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Summary

Theory in the microbial world

The microbial world is vast and important domain of apparently unfathomable complexity. The latest swathe of sequencing technology (Sogin et al. 2006; Huber et al. 2007) has confirmed what many had already predicted: there is an awful lot of different kinds of bacteria in the world. The number is unknown even in ostensibly well-studied environments and this is preventing us from understanding one of the most important and remarkable things about the microbial world: the way in which communities form and reform, and change.

For all our molecular sophistication, our analysis and understanding of the diversity and community assembly is still very primitive. Microbial ecology is perhaps in a situation analogous to that of general ecology before McArthur's first contributions; a situation described by Cody and Diamond (1975) who wrote:

in the 1950s, ecology was still mainly descriptive. It consisted of qualitative, situation-bound statements that had low predictive value, plus empirical facts that often seem to defy generalization.

(Cody & Diamond 1975)

What McArthur brought was theory, and theory is what microbial ecologists need now. Parameterized mathematical descriptions of community assembly will help us to make coherent quantitative predictions about the microbial world. These predictions can guide the exploration and manipulation of this domain.

In the search for theory, theoretical microbial ecologists have naturally looked to classical ecology for insight and inspiration (Horner-Devine et al. 2007; Prosser et al. 2007). This may be unwise.

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Publisher: Cambridge University Press
Print publication year: 2009

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References

Alonso, D., Etienne, R. S. and McKane, A. J. (2006) The merits of neutral theory. Trends in Ecology & Evolution 21, 451–457.CrossRefGoogle ScholarPubMed
Baptista, J. C. B., Sloan, W., Head, I. M. and Curtis, T. P. (2008) The species area curve is not observed or predicted in wastewater treatment plants. In Preparation.
Bell, G. (2001) Ecology – neutral macroecology. Science 293, 2413–2418.CrossRefGoogle ScholarPubMed
Bell, T., Ager, D., Song, J. I., et al. (2005) Larger islands house more bacterial taxa. Science 308, 1884.CrossRefGoogle ScholarPubMed
Brown, J. H. (2000) Macroecology. University of Chicago Press, Chicago.Google Scholar
Caswell, H. (1976) Community structure – neutral model analysis. Ecological Monographs 46, 327–354.CrossRefGoogle Scholar
Clarke, A., and Gaston, K. J. (2006) Climate, energy and diversity. Proceedings of the Royal Society B-Biological Sciences 273, 2257–2266.CrossRefGoogle ScholarPubMed
Cody, M. L. and Diamond, J. M. (1975) Robert MacArthur, 1930–1972. In: Ecology and Evolution of Communities (ed. Cody, M. L. and Diamond, J. M.), pp. 1–12. Belknap Press of Harvard University Press, Cambridge, MA.Google Scholar
Coskuner, G., Ballinger, S. J., Davenport, R. J., et al. (2005) Agreement between theory and measurement in quantification of ammonia-oxidizing bacteria. Applied and Environmental Microbiology 71, 6325–6334.CrossRefGoogle ScholarPubMed
Costa, E., Perez, J. and Kreft, J. U. (2006) Why is metabolic labour divided in nitrification? Trends in Microbiology 14, 213–219.CrossRefGoogle ScholarPubMed
Curtis, T. (2006) Microbial ecologists: it's time to ‘go large’. Nature Reviews Microbiology 4, 488.CrossRefGoogle ScholarPubMed
Curtis, T. P. and Sloan, W. T. (2005) Exploring microbial diversity – a vast below. Science 309, 1331–1333.CrossRefGoogle ScholarPubMed
Curtis, T. P., Sloan, W. T. and Scannell, J. W. (2002) Estimating prokaryotic diversity and its limits. Proceedings of the National Academy of Sciences of the United States of America 99, 10494–10499.CrossRefGoogle ScholarPubMed
Curtis, T. P., Head, I. M., Lunn, M., et al. (2006) What is the extent of prokaryotic diversity? Philosophical Transactions of the Royal Society B-Biological Sciences 361, 2023–2037.CrossRefGoogle ScholarPubMed
Dar, S. A., Yao, L., Dongen, U., Kuenen, J. G. and Muyzer, G. (2007) Analysis of diversity and activity of sulfate-reducing bacterial communities in sulfidogenic bioreactors using 16S rRNA and dsrB genes as molecular markers. Applied and Environmental Microbiology 73, 594–604.CrossRefGoogle ScholarPubMed
Elena, S. F. and Lenski, R. E. (1997) Test of synergistic interactions among deleterious mutations in bacteria. Nature 390, 395–398.CrossRefGoogle ScholarPubMed
Etienne, R. S. and Alonso, D. (2005) A dispersal-limited sampling theory for species and alleles. Ecology Letters 8, 1147–1156.CrossRefGoogle ScholarPubMed
Evans, K. L. and Gaston, K. J. (2005) Can the evolutionary-rates hypothesis explain species–energy relationships? Functional Ecology 19, 899–915.CrossRefGoogle Scholar
Finke, N., Hoehler, T. M., and Jorgensen, B. B.. (2003) Methanogenesis from methylamine and methanol at changing hydrogen concentrations. Geochimica et Cosmochimica Acta 67, A97.Google Scholar
Finke, N., Hoehler, T. M. and Jorgensen, B. B. (2007) Hydrogen ‘leakage’ during methanogenesis from methanol and methylamine: implications for anaerobic carbon degradation pathways in aquatic sediments. Environmental Microbiology 9, 1060–1071.CrossRefGoogle ScholarPubMed
Francis, C. A., Roberts, K. J., Beman, J. M., Santoro, A. E. and Oakley, B. B. (2005) Ubiquity and diversity of ammonia-oxidizing archaea in water columns and sediments of the ocean. Proceedings of the National Academy of Sciences of the United States of America 102, 14683–14688.CrossRefGoogle ScholarPubMed
Gillespie, J. H. (2004) Population Genetics: A Concise Guide. John Hopkins University Press, Baltimore, MD.Google Scholar
Gillooly, J. F., Allen, A. P., West, G. B. and Brown, J. H. (2005) The rate of DNA evolution: Effects of body size and temperature on the molecular clock. Proceedings of the National Academy of Sciences of the United States of America 102, 140–145.CrossRefGoogle ScholarPubMed
Grogan, D. W., Carver, G. T. and Drake, J. W. (2001) Genetic fidelity under harsh conditions: analysis of spontaneous mutation in the thermoacidophilic archaeon Sulfolobus acidocaldarius. Proceedings of the National Academy of Sciences of the United States of America 98, 7928–7933.CrossRefGoogle ScholarPubMed
Hallin, S., Throback, I. N., Dicksved, J. and Pell, M. (2006) Metabolic profiles and genetic diversity of denitrifying communities in activated sludge after addition of methanol or ethanol. Applied and Environmental Microbiology 72, 5445–5452.CrossRefGoogle ScholarPubMed
Hatzinikolaou, D. G., Kalogeris, E., Christakopoulos, P., Kekos, D. and Macris, B. J. (2001) Comparative growth studies of the extreme thermophile Sulfolobus acidocaldarius in submerged and solidified substrate cultures. World Journal of Microbiology & Biotechnology 17, 229–234.CrossRefGoogle Scholar
Horner-Devine, M. C., Lage, M., Hughes, J. B. and Bohannan, B. J. M. (2004) A taxa–area relationship for bacteria. Nature 432, 750–753.CrossRefGoogle ScholarPubMed
Horner-Devine, M. C., Silver, J. M., Leibold, M. A., et al. (2007) A comparison of taxon co-occurrence patterns for macro- and microorganisms. Ecology 88, 1345–1353.CrossRefGoogle ScholarPubMed
Houchmandzadeh, B. and Vallade, M. (2003) Clustering in neutral ecology. Physical Review E 68.CrossRefGoogle ScholarPubMed
Hubbell, S. P. (2001) The Unified Neutral Theory of Biodiversity and Biogeography. Princeton University Press, Princeton, NJ.Google Scholar
Huber, J. A., Welch, D. B. M., Morrison, H. G., et al. (2007) Microbial population structures in the deep marine biosphere. Science 318, 97–100.CrossRefGoogle ScholarPubMed
Huisman, J. and Weissing, F. J. (1999) Biodiversity of plankton by species oscillations and chaos. Nature 402, 407–410.CrossRefGoogle Scholar
Kibota, T. T. and Lynch, M. (1996) Estimate of the genomic mutation rate deleterious to overall fitness in E-coli. Nature 381, 694–696.CrossRefGoogle ScholarPubMed
Kondrashov, A. S. (1988) Deleterious mutations and the evolution of sexual reproduction. Nature 336, 435–440.CrossRefGoogle ScholarPubMed
Leclerc, M., Delgenes, J. P. and Godon, J. J. (2004) Diversity of the archaeal community in 44 anaerobic digesters as determined by single strand conformation polymorphism analysis and 16S rDNA sequencing. Environmental Microbiology 6, 809–819.CrossRefGoogle ScholarPubMed
MacArthur, R. (1957) On the relative abundance of bird species. Proceedings of the National Academy of Science 43, 293–295.CrossRefGoogle ScholarPubMed
MacArthur, R. and Wilson, E. (1967) The Theory of Island Biogeography. Princeton Univerity Press, Princeton, NJ.Google Scholar
Maisnier-Patin, S., Roth, J. R., Fredriksson, A., et al. (2005) Genomic buffering mitigates the effects of deleterious mutations in bacteria. Nature Genetics 37, 1376–1379.CrossRefGoogle ScholarPubMed
May, R. M. (1974) Patterns of species abundance and diversity. In: Ecology and Evolution of Communities (ed. Cody, M. L. and Diamond, J. M.), pp. 81–120 Harvard University Press, Harvard.Google Scholar
Maynard-Smith, J. (1974) Models in Ecology. Cambridge University Press, London.Google Scholar
McCarty, P. L. (1971) Energetics and bacterial growth. In: Organic Compounds in Aquatic Environments (ed. Fraust, S. D. and Hunter, J. V.). Marcel Dekker Inc, New York.Google Scholar
McCarty, P. L. (2007) Thermodynamic electron equivalents model for bacterial yield prediction. Modifications and Comparative Evaluations. Biotechnology and Bioengineering 97, 377–388.CrossRefGoogle ScholarPubMed
McHugh, S., Carton, M., Mahony, T. and O'Flaherty, V. (2003) Methanogenic population structure in a variety of anaerobic bioreactors. FEMS Microbiology Letters 219, 297–304.CrossRefGoogle Scholar
McKane, A. J., Alonso, D. and Sole, R. V. (2004) Analytic solution of Hubbell's model of local community dynamics. Theoretical Population Biology 65, 67–73.CrossRefGoogle ScholarPubMed
Mouquet, N., and Loreau, M. (2003) Community patterns in source-sink metacommunities. American Naturalist 162, 544–557.CrossRefGoogle ScholarPubMed
Neufeld, J. D. and Mohn, W. W. (2005) Unexpectedly high bacterial diversity in arctic tundra relative to boreal forest soils, revealed by serial analysis of ribosomal sequence tags. Applied and Environmental Microbiology 71, 5710–5718.CrossRefGoogle ScholarPubMed
Peters, R. H. (1991) A Critique for Ecology. Cambridge University Press, Cambridge.Google Scholar
Pounds, J. A. and Puschendorf, R. (2004) Ecology – clouded futures. Nature 427, 107–109.CrossRefGoogle ScholarPubMed
Prosser, J. I., Bohannan, B. J. M., Curtis, T. P., et al. (2007) Essay – the role of ecological theory in microbial ecology. Nature Reviews Microbiology 5, 384–392.CrossRefGoogle Scholar
Ramette, A. and Tiedje, J. M. (2007) Multiscale responses of microbial life to spatial distance and environmental heterogeneity in a patchy ecosystem. Proceedings of the National Academy of Sciences of the United States of America 104, 2761–2766.CrossRefGoogle Scholar
Rittmann, B. E. and McCarty, P. L. (2001) Environmental Biotechnology, Principles and Applications. McGraw-Hill Inc., New York.Google Scholar
Sloan, W. T., Lunn, M., Woodcock, S., et al. (2006) Quantifying the roles of immigration and chance in shaping prokaryote community structure. Environmental Microbiology 8, 732–740.CrossRefGoogle ScholarPubMed
Sloan, W. T., Woodcock, S., Lunn, M., Head, I. M. and Curtis, T. P. (2007) Modeling taxa-abundance distributions in microbial communities using environmental sequence data. Microbial Ecology 53, 443–455.CrossRefGoogle ScholarPubMed
Sogin, M. L., Morrison, H. G., Huber, J. A., et al. (2006) Microbial diversity in the deep sea and the underexplored ‘rare biosphere’. Proceedings of the National Academy of Sciences of the United States of America 103, 12115–12120.CrossRefGoogle Scholar
Strous, M., Fuerst, J. A., Kramer, E. H. M., et al. (1999) Missing lithotroph identified as new planctomycete. Nature 400, 446–449.CrossRefGoogle ScholarPubMed
Tilman, D. (2004) Niche tradeoffs, neutrality, and community structure: a stochastic theory of resource competition, invasion, and community assembly. Proceedings of the National Academy of Sciences of the United States of America 101, 10854–10861.CrossRefGoogle ScholarPubMed
Valentine, D. L. (2007) Adaptations to energy stress dictate the ecology and evolution of the Archaea. Nature Reviews Microbiology 5, 316–323.CrossRefGoogle ScholarPubMed
Vallade, M. and Houchmandzadeh, B. (2003) Analytical solution of a neutral model of biodiversity. Physical Review E 68.CrossRefGoogle ScholarPubMed
Volkov, I., Banavar, J. R., Hubbell, S. P. and Maritan, A. (2003) Neutral theory and relative species abundance in ecology. Nature 424, 1035–1037.CrossRefGoogle ScholarPubMed
Wilson, E. O. (1998) Consilience: The Unity of Knowledge. Vintage, New York.Google Scholar
Woodcock, S., Curtis, T. P., Head, I. M., Lunn, M. and Sloan, W. T. (2006) Taxa-area relationships for microbes: the unsampled and the unseen. Ecology Letters 9, 805–812.CrossRefGoogle ScholarPubMed
Woodcock, S., Gast, C. J., Bell, T., et al. (2007) Neutral assembly of bacterial communities. FEMS Microbial Ecology 62, 171–180.CrossRefGoogle ScholarPubMed

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