| scholarly article | Q13442814 |
| P356 | DOI | 10.1111/1462-2920.13028 |
| P698 | PubMed publication ID | 26287440 |
| P50 | author | Sylvie Estrela | Q41556286 |
| P2093 | author name string | Benjamin Kerr | |
| J Jeffrey Morris | |||
| P2860 | cites work | tragedy of the commons | Q334622 |
| Unique glycine-activated riboswitch linked to glycine-serine auxotrophy in SAR11 | Q24650852 | ||
| Structure and evolution of Streptomyces interaction networks in soil and in silico | Q27320756 | ||
| Metabolic and demographic feedbacks shape the emergent spatial structure and function of microbial communities | Q27323496 | ||
| Evolution of cross-feeding in microbial populations | Q28273191 | ||
| The fate of cooperation during range expansions | Q28489085 | ||
| The Black Queen Hypothesis: evolution of dependencies through adaptive gene loss | Q28730844 | ||
| Social evolution in multispecies biofilms | Q28742796 | ||
| A general model for the evolution of mutualisms. | Q33342780 | ||
| Population dynamics constrain the cooperative evolution of cross-feeding | Q33398050 | ||
| Syntrophic exchange in synthetic microbial communities | Q33665680 | ||
| Rapid evolution of stability and productivity at the origin of a microbial mutualism | Q33719701 | ||
| Dependence of the cyanobacterium Prochlorococcus on hydrogen peroxide scavenging microbes for growth at the ocean's surface. | Q33815345 | ||
| Metabolic resource allocation in individual microbes determines ecosystem interactions and spatial dynamics | Q33900751 | ||
| Less is more: selective advantages can explain the prevalent loss of biosynthetic genes in bacteria. | Q51438302 | ||
| Coexistence of evolving bacteria stabilized by a shared Black Queen function. | Q54286132 | ||
| Our Current Understanding of Mutualism | Q56091353 | ||
| Loss of lipid synthesis as an evolutionary consequence of a parasitic lifestyle. | Q33928351 | ||
| Species interactions alter evolutionary responses to a novel environment | Q34276938 | ||
| The evolution of cooperation. | Q34330940 | ||
| Erosion of functional independence early in the evolution of a microbial mutualism. | Q34383891 | ||
| Sympatric speciation in a bacterial endosymbiont results in two genomes with the functionality of one. | Q34436167 | ||
| Evolutionary limits to cooperation in microbial communities | Q34752307 | ||
| SAR11 marine bacteria require exogenous reduced sulphur for growth | Q34761326 | ||
| The consequences of genetic drift for bacterial genome complexity | Q34985390 | ||
| Quorum sensing triggers the stochastic escape of individual cells from Pseudomonas putida biofilms | Q35023061 | ||
| Spatial population expansion promotes the evolution of cooperation in an experimental Prisoner's Dilemma | Q35516454 | ||
| Sociality in Escherichia coli: Enterochelin Is a Private Good at Low Cell Density and Can Be Shared at High Cell Density. | Q35682345 | ||
| A quantitative test of population genetics using spatiogenetic patterns in bacterial colonies. | Q36063708 | ||
| The evolution of interspecific mutualisms | Q36211821 | ||
| Vitamins in the sea. | Q36212981 | ||
| Metabolic specialization and the assembly of microbial communities | Q36330218 | ||
| Public good dynamics drive evolution of iron acquisition strategies in natural bacterioplankton populations | Q36471250 | ||
| Social evolution theory for microorganisms. | Q36538101 | ||
| Range expansion promotes cooperation in an experimental microbial metapopulation. | Q36820204 | ||
| Defined spatial structure stabilizes a synthetic multispecies bacterial community | Q36984976 | ||
| Bacterial cheating drives the population dynamics of cooperative antibiotic resistance plasmids | Q37189738 | ||
| Spatial self-organization favors heterotypic cooperation over cheating | Q37295444 | ||
| Genetic drift opposes mutualism during spatial population expansion | Q37519718 | ||
| Ecological interactions drive evolutionary loss of traits | Q38022744 | ||
| Black Queen evolution: the role of leakiness in structuring microbial communities | Q38528691 | ||
| Fitness and stability of obligate cross-feeding interactions that emerge upon gene loss in bacteria | Q38915483 | ||
| Coexistence of two competitors on one resource and one inhibitor: a chemostat model based on bacteria and antibiotics | Q39800210 | ||
| Plant-fungal ecology. Niche engineering demonstrates a latent capacity for fungal-algal mutualism. | Q39938657 | ||
| Snowdrift game dynamics and facultative cheating in yeast | Q41200215 | ||
| From metabolism to ecology: cross-feeding interactions shape the balance between polymicrobial conflict and mutualism | Q41556252 | ||
| Siderophores from neighboring organisms promote the growth of uncultured bacteria | Q41846710 | ||
| An ecological network of polysaccharide utilization among human intestinal symbionts | Q41955485 | ||
| The origins of cooperative bacterial communities | Q42142483 | ||
| Emergent cooperation in microbial metabolism | Q42397954 | ||
| Distinguishing mechanisms for the evolution of co-operation | Q45002918 | ||
| Genetics of mutualism: the evolution of altruism between species | Q46406172 | ||
| Habitat structure and the evolution of diffusible siderophores in bacteria. | Q46834746 | ||
| P433 | issue | 5 | |
| P304 | page(s) | 1415-1427 | |
| P577 | publication date | 2015-08-19 | |
| P1433 | published in | Environmental Microbiology | Q15752447 |
| P1476 | title | Private benefits and metabolic conflicts shape the emergence of microbial interdependencies. | |
| P478 | volume | 18 |
| Q33595748 | A passive mutualistic interaction promotes the evolution of spatial structure within microbial populations |
| Q91362713 | Bacterial siderophores in community and host interactions |
| Q41688854 | Beyond the Black Queen Hypothesis |
| Q44718300 | Black Queen markets: commensalism, dependency, and the evolution of cooperative specialization in human society |
| Q55447824 | Community interactions and spatial structure shape selection on antibiotic resistant lineages. |
| Q45950268 | Ecological selection of siderophore-producing microbial taxa in response to heavy metal contamination. |
| Q98394817 | Enhanced nutrient uptake is sufficient to drive emergent cross-feeding between bacteria in a synthetic community |
| Q92982102 | Environmentally Mediated Social Dilemmas |
| Q46250203 | Evolution on the bright side of life: microorganisms and the evolution of mutualism |
| Q38716851 | Experimental evolution and the adjustment of metabolic strategies in lactic acid bacteria |
| Q89877030 | Functional traits of the gut microbiome correlated with host lipid content in a natural population of Drosophila melanogaster |
| Q46259934 | Genome-driven evolutionary game theory helps understand the rise of metabolic interdependencies in microbial communities. |
| Q91821677 | Individual- versus group-optimality in the production of secreted bacterial compounds |
| Q91666747 | Labour sharing promotes coexistence in atrazine degrading bacterial communities |
| Q64235438 | Less Is More: Genome Reduction and the Emergence of Cooperation-Implications into the Coevolution of Microbial Communities |
| Q90376461 | Model Microbial Consortia as Tools for Understanding Complex Microbial Communities |
| Q90612469 | Multi-faceted approaches to discovering and predicting microbial nutritional interactions |
| Q52333811 | No effect of intraspecific relatedness on public goods cooperation in a complex community. |
| Q45186263 | Paradoxes in leaky microbial trade |
| Q46252456 | Recipient-Biased Competition for an Intracellularly Generated Cross-Fed Nutrient Is Required for Coexistence of Microbial Mutualists |
| Q57942227 | Selection for Gaia across Multiple Scales |
| Q92146671 | Syntrophy emerges spontaneously in complex metabolic systems |
| Q42694306 | The Exometabolome of Two Model Strains of the Roseobacter Group: A Marketplace of Microbial Metabolites |
| Q90571759 | The microbial exometabolome: ecological resource and architect of microbial communities |
| Q33707113 | Why Quorum Sensing Controls Private Goods |
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