Abstract

Empirical observations have shown that cooperative partners can compete for common resources, but what factors determine whether partners cooperate or compete remain unclear. Using the reciprocal fig–fig wasp mutualism, we show that nonlinear amplification of interference competition between fig wasps—which limits the fig wasps' ability to use a common resource (i.e. female flowers)—keeps the common resource unsaturated, making cooperation locally stable. When interference competition was manually prevented, the fitness correlation between figs and fig wasps went from positive to negative. This indicates that genetic relatedness or reciprocal exchange between cooperative players, which could create spatial heterogeneity or self-restraint, was not sufficient to maintain stable cooperation. Moreover, our analysis of field-collected data shows that the fitness correlation between cooperative partners varies stochastically, and that the mainly positive fitness correlation observed during the warm season shifts to a negative correlation during the cold season owing to an increase in the initial oviposition efficiency of each fig wasp. This implies that the discriminative sanction of less-cooperative wasps (i.e. by decreasing the egg deposition efficiency per fig wasp) but reward to cooperative wasps by fig, a control of the initial value, will facilitate a stable mutualism. Our finding that asymmetric interaction leading to an indeterminate fitness interaction between symbiont (i.e. cooperative actors) and host (i.e. recipient) has the potential to explain why conflict has been empirically observed in both well-documented intraspecific and interspecific cooperation systems.

Highlights

  • Explaining the evolution of cooperation and how cooperative systems achieve stability remains one of the most debated problems in both the biological and the social science communities [1,2]

  • Empirical observation and data analysis have further shown that self-restraint of cooperative actors or spatial heterogeneity created by recipients cannot sufficiently maintain the stable cooperative interaction in both intraspecific and interspecific cooperation systems

  • With simultaneous entry of pollinators, the nonlinear amplification of interference competition among the foundresses cancelled out extra pollination and oviposition after the number of foundresses reached a threshold

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Summary

INTRODUCTION

Explaining the evolution of cooperation and how cooperative systems achieve stability remains one of the most debated problems in both the biological and the social science communities [1,2]. Empirical observation and data analysis have further shown that self-restraint of cooperative actors or spatial heterogeneity created by recipients cannot sufficiently maintain the stable cooperative interaction in both intraspecific and interspecific cooperation systems. Further quantitative examination has shown that neither the hypothesized spatial heterogeneity (structural barrier of flowers such as the heterogeneity in style or pedicel length) created by plants nor the evolutionary constraint of symbionts in the fig–fig wasp mutualism to be sufficient to prevent fig wasps from over-using female flowers at the expense of viable seeds [9,24,34,35]. Following from our previous paper [36], in this paper we would like to explore the remaining problem on why both cooperative (i.e. positive fitness correlation) and conflict interactions (i.e. negative fitness correlation) can be observed between figs and their pollinator wasps under the interference competition among the fig wasps

Study species
Introduction method
Natural data collection
Correlation analysis
ANALYSES AND RESULTS
DISCUSSION
Full Text
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