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Multiple Mating and Its Relationship to Alternative Modes of Gestation in Male-Pregnant Versus Female-Pregnant fish Species

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Multiple Mating and Its Relationship to Alternative Modes of Gestation in Male-Pregnant Versus Female-Pregnant fish Species Multiple mating and its relationship to alternative modes of gestation in male-pregnant versus female-pregnant fish species John C. Avise1 and Jin-Xian Liu Department of Ecology and Evolutionary Biology, University of California, Irvine, CA 92697 Contributed by John C. Avise, September 28, 2010 (sent for review August 20, 2010) We construct a verbal and graphical theory (the “fecundity-limitation within which he must incubate the embryos that he has sired with hypothesis”) about how constraints on the brooding space for em- one or more mates (14–17). This inversion from the familiar bryos probably truncate individual fecundity in male-pregnant and situation in female-pregnant animals apparently has translated in female-pregnant species in ways that should differentially influence some but not all syngnathid species into mating systems char- selection pressures for multiple mating by males or by females. We acterized by “sex-role reversal” (18, 19): a higher intensity of then review the empirical literature on genetically deduced rates of sexual selection on females than on males and an elaboration of fi multiple mating by the embryo-brooding parent in various fish spe- sexual secondary traits mostly in females. For one such pipe sh cies with three alternative categories of pregnancy: internal gesta- species, researchers also have documented that the sexual- tion by males, internal gestation by females, and external gestation selection gradient for females is steeper than that for males (20). More generally, fishes should be excellent subjects for as- (in nests) by males. Multiple mating by the brooding gender was fl common in all three forms of pregnancy. However, rates of multiple sessing how alternative types of pregnancy might in uence the mating as well as mate numbers for the pregnant parent averaged evolution of genetic mating systems and sexual selection on males versus females, because most fish have high fecundities higher in species with external as compared with internal male preg- (many embryos per brood) and because both internal male nancy, and also for dams in female-pregnant species versus sires in pregnancy and female pregnancy are displayed by various taxa. EVOLUTION male-pregnant species. These outcomes are all consistent with the Furthermore, males in many other taxonomic families of fishes theory that different types of pregnancy have predictable conse- “ ” ’ display what can be interpreted as external pregnancy wherein quences for a parent s brood space, its effective fecundity, its oppor- each “bourgeois male” (21) builds a nest in which he tends the tunities and rewards for producing half-sib clutches, and thereby embryos from one or more females whose eggs he himself has its exposure to selection pressures for seeking multiple mates. Over- mostly fertilized (22–25). Both internal and external pregnancy fi all, we try to t these fecundity-limitation phenomena into a broader in fishes imply a substantial energetic investment in offspring conceptual framework for mating-system evolution that also in- care by the brooding sex. cludes anisogamy, sexual-selection gradients, parental investment, For any type of pregnancy, multiple successful mating by the and other selective factors that can influence the relative proclivities adult caregiver is relatively straightforward to detect in nature of males versus females to seek multiple sexual partners. via molecular parentage analyses because each resulting brood of half-sib embryos is physically associated with its pregnant sire or genetic parentage | mating systems | microsatellites | pregnancy | sexual pregnant dam. By contrast, documenting the frequency of mul- selection tiple mating by members of the nonpregnant sex is much more difficult because each such individual may have parented addi- any selective factors can influence the evolution of differ- tional broods that did not happen to be included in the genetic Mences in mating tactics between males and females. At the assays, and thus remain undetected. Thus arises another sexual ultimate level of explanation, anisogamy (the pronounced size asymmetry relevant to the current discussion: For purely logis- difference between male and female gametes) helps to set the tical reasons, molecular parentage analyses usually are best- evolutionary stage by making females intrinsically more fecundity- suited for assessing rates of multiple paternity within the broods limited than males (1, 2). At a penultimate level of explanation, of female-pregnant species (i.e., multiple mating by the females) this potential fertility difference between the sexes often translates and multiple maternity within the broods of male-pregnant into steeper sexual-selection gradients (3) for males than for species (i.e., multiple mating by the males), rather than vice versa females, meaning that males in many species tend to profitmore (26, 27). than females (in terms of genetic fitness) from having multiple Here we take advantage of all these facts by reviewing genetic fi mates (4). Because a male’s reproductive success can increase data on multiple mating by the brooding sex in sh species with fi ’ greatly with mate count whereas a female’s reproductive success is several alternative forms of pregnancy. We de ne an individual s limited mostly by her fecundity regardless of mate number, males fecundity (or maximum reproductive potential) as the number of in many animal species presumably are under stronger selection gametes it produces that stand a reasonably good prospect, given ’ pressure than females to seek multiple sexual partners. Finally, the species biology, of contributing to successful embryos during selection pressures on male versus female mating behaviors can a breeding season or episode. Thus, in effect, both anisogamy further be impacted by numerous more proximate considerations and pregnancy can be thought of as fecundity-truncating phe- such as operational sex ratios in local populations (5, 6), relative nomena for the gender in question, all else being equal. In other levels of parental investment in offspring (7, 8), and other species- words, brood space constrains the number of embryos that specific ecological and genetic factors that can differentially im- a pregnant individual can parent, and the effect probably is more pact the two sexes’ potential reproductive rates (9, 10) or their variances in reproductive success (11, 12). In taxa such as Syngnathidae (pipefishes and seahorses) that Author contributions: J.C.A. designed research; J.C.A. and J.-X.L. performed research; J.-X.L. display the phenomenon of male pregnancy, some of the evo- analyzed data; and J.C.A. wrote the paper. lutionary ground rules described above can shift dramatically The authors declare no conflict of interest. (reviewed in ref. 13). In the ≈200 extant syngnathid species, 1To whom correspondence should be addressed. E-mail: [email protected]. a male in effect is fecundity-limited (sometimes even more so This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10. than a typical female) due to the finite size of the brood pouch 1073/pnas.1013786107/-/DCSupplemental. www.pnas.org/cgi/doi/10.1073/pnas.1013786107 PNAS Early Edition | 1of6 Downloaded by guest on October 1, 2021 extreme for internal brooders than external brooders. However, much as does the greater access to opposite-sex gametes that for any kind of pregnancy, each individual’s maximum fecundity multiple mating provides. Of course, multiple mating by either also depends on its mating habits. For example, in species with sex can incur costs as well, such as the time and energy required female pregnancy, a polygynous male clearly has a much higher to secure mates and the increased chance of contracting a sex- reproductive potential than a monogamous male or a monoga- ually transmitted disease. mous or polyandrous female. [Here we define a polygamous In any event, to distinguish between fecundity limitations specimen (a polygynous male or a polyandrous female) as an in- per se and other hypotheses for any disparity between rates of dividual that has two or more successful mates during a breeding multiple mating by males versus females, it should be helpful to season or episode, whereas a monogamous specimen has only one compare the incidences of multiple mating in numerous related such mate]. In some but not all cases, an individual’s maximum species in which an individual’s maximum fecundity varies pre- fecundity also depends upon that of its pregnant mate(s). For dictably as a function of the type of pregnancy. Here we in- example, in any species with internal pregnancy, the maximum troduce this approach by comparing genetically determined mate fecundity of a monogamous individual (but not a polygamous one) numbers and rates of multiple mating for (i) males in fish species is physically limited by the size of its mate’s brood chamber, which with internal versus external male pregnancy, and (ii) males in places a ceiling on the number of embryos that can be brooded male-pregnant fish species vis-à-vis females in female-pregnant successfully. Furthermore, that number of embryos is likely to be fishes. We review the genetic literature on rates of multiple lower than the number of eggs a female can produce, because maternity within broods of male-pregnant fish species and rates embryos take up more space than do unfertilized eggs. The broader of multiple paternity within broods of female-pregnant fishes. point is that each type of pregnancy in effect can truncate the fe- We then
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