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. 2017 Jan 13:6:e21673.
doi: 10.7554/eLife.21673.

Nomadic-colonial life strategies enable paradoxical survival and growth despite habitat destruction

Affiliations

Nomadic-colonial life strategies enable paradoxical survival and growth despite habitat destruction

Zhi Xuan Tan et al. Elife. .

Abstract

Organisms often exhibit behavioral or phenotypic diversity to improve population fitness in the face of environmental variability. When each behavior or phenotype is individually maladaptive, alternating between these losing strategies can counter-intuitively result in population persistence-an outcome similar to the Parrondo's paradox. Instead of the capital or history dependence that characterize traditional Parrondo games, most ecological models which exhibit such paradoxical behavior depend on the presence of exogenous environmental variation. Here we present a population model that exhibits Parrondo's paradox through capital and history-dependent dynamics. Two sub-populations comprise our model: nomads, who live independently without competition or cooperation, and colonists, who engage in competition, cooperation, and long-term habitat destruction. Nomads and colonists may alternate behaviors in response to changes in the colonial habitat. Even when nomadism and colonialism individually lead to extinction, switching between these strategies at the appropriate moments can paradoxically enable both population persistence and long-term growth.

Keywords: Ecology; Evolutionary Biology; Parrondo's paradox; computational biology; ecology; none; systems biology.

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Conflict of interest statement

No competing interests declared.

Figures

Figure 1.
Figure 1.. In the absence of switching, (a) eventual extinction for both strategies vs (b) survival for the colonial strategy.
Initial conditions for both are n1=2, n2=2, K=5. Shared parameters are rs=0, r1=1, r2=10. For (a), A=1.001. For (b), A=0.5.
Figure 2.
Figure 2.. Behavioral switching which results in (a) extinction vs (b) survival.
Initial conditions for both are n1=2, n2=2, K=5. Shared parameters are rs=1000, r1=1, r2=10. For (a), L1=3, L2=4.5. For (b), L1=3, L2=4.
Figure 3.
Figure 3.. Long-term growth through strategic alternation.
Initial conditions are n1=0, n2=2, K=5. Parameters are A=1.001, L1=3, L2=4, rs=1000, r1=1, r2=10.
Figure 4.
Figure 4.. Zoomed-in portion of Figure 5 that shows the mechanism behind the spikes in n1.
When n2 is large, switching takes longer, causing a drop in K, and a large increase in n1.
Figure 5.
Figure 5.. Long-term growth through strategic alternation, up to t=1000.
Initial conditions are n1=0, n2=2, K=5. Parameters are A=1.001, rs=1000, r1=1, r2=10.
Figure 6.
Figure 6.. Survival through periodic alternation under slow habitat change.
Parameters for (a) are rs=10000, r1=10, r2=100,L1=3, L2=3.083. For (b), rs=100000, r1=100, r2=1000,L1=3, L2=3.008. Shared parameters are Kmax=20, A=1.001.
Figure 7.
Figure 7.. Long-term growth through strategic alternation with a bounded carrying capacity.
Initial conditions are n1=0, n2=2, K=5, shared parameters are A=1.001. For (a), Kmax=20, rs=1000, r1=1, r2=10 (fast habitat change). For (b), Kmax=7.5, rs=10000, r1=10, r2=100 (slow habitat change).
Appendix 1—figure 1.
Appendix 1—figure 1.. An example of switching from colonialism to nomadism.
t1 marks the start of the switch, t2 marks the end. Other parameters are A=1.001, rs=1000, r1=1, r2=10.
Appendix 1—figure 2.
Appendix 1—figure 2.. An example of switching from nomadism to colonialism.
t1 marks the start of the switch, t2 marks the end. Other parameters are A=1.001, rs=1000, r1=1, r2=10.

References

    1. Abbott D. Asymmetry and disorder: A decade of parrondo'S PARADOX. Fluctuation and Noise Letters. 2010;09:129–156. doi: 10.1142/S0219477510000010. - DOI
    1. Acar M, Mettetal JT, van Oudenaarden A. Stochastic switching as a survival strategy in fluctuating environments. Nature Genetics. 2008;40:471–475. doi: 10.1038/ng.110. - DOI - PubMed
    1. Annesley SJ, Fisher PR. Dictyostelium discoideum--a model for many reasons. Molecular and Cellular Biochemistry. 2009;329:73–91. doi: 10.1007/s11010-009-0111-8. - DOI - PubMed
    1. Baldauf SL, Doolittle WF. Origin and evolution of the slime molds (Mycetozoa) PNAS. 1997;94:12007–12012. doi: 10.1073/pnas.94.22.12007. - DOI - PMC - PubMed
    1. Bastidas RJ, Heitman J. Trimorphic stepping stones pave the way to fungal virulence. PNAS. 2009;106:351–352. doi: 10.1073/pnas.0811994106. - DOI - PMC - PubMed

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