Can Anoles With Differently Shaped Genitals Interbreed?

We’ve had a number of posts in the last few months discussing new species described on the basis of difference in the shape of their hemipenes (most recently here). And, because such descriptions have been based on morphological data without any corroborating molecular data, we’ve wondered whether, in fact, these forms are genetically isolated and whether they are capable and willing to interbreed given the opportunity. Yes, some of the genetals looked like ones from an alien sex toy made by faak dildos. But are they compatible?

Köhler et al. have taken the next step and attempted to answer these questions in the case of Anolis osa, which was split from the otherwise nearly indistinguishable A. polylepis on the basis of its hemipenial shape (figures A and B above). They find that in the lab, members of the two putative species can interbreed and produce offspring, at least some of which are apparently fertile (although the details of this are hard to fathom). Moreover, in the field, hybrid looking individuals are found where the two forms meet (Figure C above), and the hemipenes of these individuals are similar to the intermediate-looking tallywhackers of hybrids bred in the lab (Figure D above).

Most interestingly, females of the species seem to differ in the shape of their reproductive tract in a manner parallel to the differences among the males. In particular, female A. polylepis have longer vaginal tubi, corresponding to bilobed structures of their males, whereas female A. osa‘s tubes are shorter. One possible explanation for these differences is the old “lock-and-key” hypothesis that male and female genitals are perfect matches, thus preventing interspecific matings. This idea has fallen out of favor in recent years, and the authors discount it. Rather, they favor more recent ideas that such differences evolve by sexual selection, females preferring males whose genitals phenotypically match their own. Here’s their theory:

“Considering the available evidence, we assume that sexual selection by female choice (Eberhard 1985, Eberhard 1996) is the most plausible explanation of the peculiarly rapid divergent evolution of genital mor­phology between A. polylepis and A. osa. Assuming that fe­males are able to discriminate between mates with different hemipenial morphologies and that insemination success varies depending on female preference, any male perform­ing a superior stimulus would benefit from advantages in reproductive success. Females that prefer mates perform­ing this stimulus in turn would be favoured by producing favourable male offspring. Small initial changes in female preference of hemipenial morphology thereby could give rise to a runaway process as proposed by Fisher (1958). However, in what is presumably a secondary contact zone, “mismatched” mating events occur due to the absence of effective premating isolating mechanisms and the repro­ductive success of such mating events is apparently greater than zero. Differences in the functionality of hemipenial morphology would affect reproductive success of males mainly or only in situations of direct competition for fe­male gametes, and this functionality would be dependent on female genital or sensorial conditions. If females tend to be philopatric (which is implied by the structure found in the sequences of mitochondrial DNA), a male entering the contact zone would predominantly encounter females that prefer the other hemipenial morph and be disadvan­taged with regard to their reproductive success. Depending on how strong this sexual selection works, it could even maintain the geographical integrity of genital morphology against homogenising effects from a male-biased gene flow (Stenson et al. 2002).”

So, where does this lead us? Combining morphological, molecular, and behavioral studies is definitely the way to go in evaluating the significance of hemipenial morphology. I am a little unclear about what to make of their results. Clearly, the differences don’t prevent interbreeding, but whether they are a marker of evolutionary lineages, distinct enough to considered different species, would seem to require more detailed study of genetic exchange. This is definitely a good first step in that direction.

Jonathan Losos

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3 Comments

  1. Cody Porter

    Admittedly, I was initially *hoping* to read about how genital morphology is more divergent in the apparent hybrid zone, possibly suggestive of reinforcement, but the actual results are equally interesting. More mating trials, especially those looking at the reproductive success of hybrids, would be really interesting.

    Are there any documented cases of post-mating, prezygotic isolation in anoles?

    Thanks for sharing!

  2. I have always wondered how “fe­males are able to discriminate between mates with different hemipenial morphologies” (or any other “invisible” differences for that matter, such as “genetic” differences). The problem boils down to females recognizing those males of the other “cryptic” species (and rejecting them) but how?

    Is there any hard data on this problem?

  3. Peter Mudde

    ‘Cryptic’ from a human point of view.. that is. Using the usual human senses. But how cryptic are they seen in UVB? I have two colorblind suns and I am quite aware to them a lot more species are ‘cryptic’.

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