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A General Explanation for the Persistence of Reproductive Interference
The American Naturalist
|July 19, 2019
Summary
Reproductive interference persists because males cannot distinguish similar-looking females, creating an evolutionary catch-22. This hinders the evolution of male mate recognition and reproductive character displacement in damselflies.
Area of Science:
- Evolutionary biology
- Behavioral ecology
- Speciation research
Background:
- Reproductive interference is common, contradicting evolutionary theory predicting its elimination via reproductive character displacement (RCD).
- A persistent evolutionary dilemma may arise when females of sympatric species are phenotypically similar, impeding male mate recognition (MR) evolution.
- This creates a cycle where MR cannot evolve without further female phenotype divergence, and vice versa.
Purpose of the Study:
- To test the "evolutionary catch-22" hypothesis explaining persistent reproductive interference.
- To investigate the role of female phenotype similarity and male mate recognition in reproductive isolation.
- To examine evidence for reproductive character displacement in rubyspot damselflies (Hetaerina spp.).
Main Methods:
- Analyzing data from rubyspot damselflies (Hetaerina spp.).
- Assessing the breakdown of reproductive isolation with increasing interspecific female phenotype similarity.
- Comparing allopatric and sympatric populations to detect RCD.
Main Results:
- Reproductive isolation decreased significantly as female phenotypes became more similar between species.
- No evidence of RCD was found when comparing allopatric and sympatric populations.
- Divergence in female coloration and male MR in allopatry appears to dictate reproductive isolation upon secondary contact.
Conclusions:
- The "evolutionary catch-22" hypothesis provides a robust explanation for persistent reproductive interference.
- When reproductive isolation relies on male mate recognition and sympatric females are phenotypically similar, interference endures.
- This highlights the complex interplay between sexual selection and speciation in natural populations.
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