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Evolutionary Ecology

, Volume 30, Issue 2, pp 221–234 | Cite as

Experimental evidence that evolution by niche construction affects dissipative ecosystem dynamics

  • Claire Marie LoudonEmail author
  • Blake Matthews
  • Duygu Sevgi Sevilgen
  • Bas. W. Ibelings
Original Paper

Abstract

Evolution by niche construction occurs when organism-mediated modification of the environment causes an evolutionary response. Physicists have postulated that evolution in general, and evolution mediated via feedbacks between organisms and their environment in particular (i.e. evolution by niche construction), could increase the capacity of biological systems to dissipate free energy in an open thermodynamic system, and help them maintain a state far from thermodynamic equilibrium. Here, we propose using the bacterium Pseudomonas fluorescens (strain SBW25) as a model system to experimentally test theories in both evolutionary biology (e.g. niche construction) and physics (e.g. dissipative systems theory). P. fluorescens rapidly and predictably evolves multiple strategies for exploiting oxygen in unmixed culture flasks. This evolutionary dynamic is mediated by feedbacks between the modification of the oxygen gradient by P. fluorescens and the ecological and evolutionary responses of Pseudomonas to modified environmental conditions. To confirm this, we experimentally manipulated two aspects of the system that influence the strength of the feedback between P. fluorescens and oxygen gradients in the system. First, we inhibited the metabolism of the strain used to inoculate the cultures, and, second, we disturbed the formation of mats at the air–liquid interface. Overall, we found convincing experimental evidence of evolution by niche construction, and conclude that this study system is amenable to experimental investigations of both niche construction and dissipative systems theory.

Keywords

Non-equilibrium thermodynamics Dissipative ecosystems Evolution by niche construction Entropy Pseudomonas fluorescens SBW25 

Notes

Acknowledgments

CML is grateful to Dirk De Beer for hospitality received at the Max Planck institute for Marine Microbiology in Bremen and to the Academic Society of Geneva for an additional support Grant which made this work possible. The authors are also grateful to two anonymous reviewers for suggestions which improved this manuscript.

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Copyright information

© Springer International Publishing Switzerland 2015

Authors and Affiliations

  • Claire Marie Loudon
    • 1
    • 2
    • 3
    Email author
  • Blake Matthews
    • 4
  • Duygu Sevgi Sevilgen
    • 3
  • Bas. W. Ibelings
    • 1
  1. 1.Institut F.A. ForelUniversité de GenèveGenèveSwitzerland
  2. 2.New Zealand Institute for Advanced StudyMassey UniversityAucklandNew Zealand
  3. 3.Microsensor GroupMax Planck Institute for Marine MicrobiologyBremenGermany
  4. 4.EAWAGCenter for Ecology, Evolution & BiogeochemistryKastanienbaumSwitzerland

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