The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Patterns and mechanisms of genetic and phenotypic differentiation in marine microbes
Open accessAbstract
Microbes in the ocean dominate biogeochemical processes and are far more diverse than anticipated. Thus, in order to understand the ocean system, we need to delineate microbial populations with predictable ecological functions. Recent observations suggest that ocean communities comprise diverse groups of bacteria organized into genotypic (and phenotypic) clusters of closely related organisms. Although such patterns are similar to metazoan communities, the underlying mechanisms for microbial communities may differ substantially. Indeed, the potential among ocean microbes for vast population sizes, extensive migration and both homologous and illegitimate genetic recombinations, which are uncoupled from reproduction, challenges classical population models primarily developed for sexually reproducing animals. We examine possible mechanisms leading to the formation of genotypic clusters and consider alternative population genetic models for differentiation at individual loci as well as gene content at the level of whole genomes. We further suggest that ocean bacteria follow at least two different adaptive strategies, which constrain rates and bounds of evolutionary processes: the ‘opportuni-troph’, exploiting spatially and temporally variable resources; and the passive oligotroph, efficiently using low nutrient concentrations. These ecological lifestyle differences may represent a fundamental divide with major consequences for growth and predation rates, genome evolution and population diversity, as emergent properties driving the division of labour within microbial communities.
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Cites
Prokaryotes: The unseen majority
Whitman, W. B., Coleman, D. C., & Wiebe, W. J. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.12.6578 · Cited by 4,871 · cited 3×
“In open ocean and coastal regions, it is typically approximately 10 5 and 10 6 cells ml K1 , respectively (Whitman et al. 1998).”
BackgroundInfluentialEnvironmental genome shotgun sequencing of the sargasso sea
Venter, J. C., Remington, K., Heidelberg, J. F., Halpern, A. L., Rusch, D., Eisen, J. A., Wu, D., Paulsen, I., Nelson, K. E., Nelson, W., et al. (2004) · Science · doi:10.1126/science.1093857 · Cited by 4,376
SAR11 clade dominates ocean surface bacterioplankton communities
Morris, R. M., Rappé, M. S., Connon, S. A., Vergin, K. L., Siebold, W. A., Carlson, C. A., & Giovannoni, S. J. (2002) · Nature · doi:10.1038/nature01240 · Cited by 1,129
Cited by
Life in the “plastisphere”: microbial communities on plastic marine debris
Zettler, E. R., Mincer, T. J., & Amaral-Zettler, L. A. (2013) · Environmental Science & Technology · doi:10.1021/es401288x · Cited by 3,368
Marine viruses — major players in the global ecosystem
Suttle, C. A. (2007) · Nature Reviews Microbiology · doi:10.1038/nrmicro1750 · Cited by 3,157
Oberbeckmann, S., Osborn, A. M., & Duhaime, M. B. (2016) · PLOS ONE · doi:10.1371/journal.pone.0159289 · Cited by 572
Delacuvellerie, A., Cyriaque, V., Gobert, S., Benali, S., & Wattiez, R. (2019) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2019.120899 · Cited by 422
Horizontal gene transfer and the evolution of bacterial and archaeal population structure
Polz, M. F., Alm, E. J., & Hanage, W. P. (2013) · Trends in Genetics · doi:10.1016/j.tig.2012.12.006 · Cited by 425
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Metadata
- Authors
- Polz, M. F., Hunt, D. E., Preheim, S. P., & Weinreich, D. M.
- Venue
- Philosophical Transactions of the Royal Society B: Biological Sciences
- Publisher
- The Royal Society
- Published
- 2006-10-06
- Volume
- 361
- Issue
- 1475
- Pages
- 2009-2021
- ISSN
- 0962-8436 (ISSN-L)
- 1471-2970
- OpenAlex
- W2135329955
- Cited by
- 197
- References
- 3
- FWCI
- 6.05
- Type
- journal article
- Language
- en
- Open access
- green
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