Pollinating fig wasps’ simple solutions to complex sex ratio problems: a review

Local mate competition (LMC) favours female biased clutch sex ratios because it reduces competition between brothers and provides extra mating opportunities for sons. Fig wasps seem to fit LMC model assumptions and lay female-biased sex ratios as predicted. These female biased sex ratios increase fitness greatly. In line with predictions, their sex ratios become less female-biased as the number of mothers laying in the same fig increases. However, this variation results in comparatively small fitness benefits compared to just biased ratios and data suggest substantial mismatches with LMC theory. The mismatches are due to several factors. (1) Multiple foundresses typically lay too many daughters. (2) Single foundress sex ratios are explained by sequential oviposition and ladies-last models. (3) Mortality that typically exceeds 10% may decouple the link between primary sex ratios, the focus of model predictions, and secondary sex ratios of adult wasps that are counted by researchers. (4) Model assumptions are frequently violated: (a) clutch sizes are unequal, (b) oviposition may not be simultaneous (c) cryptic/multiple wasp species inhabit the same host, (d) foundress numbers are systematically undercounted, (e) inbreeding coefficient calculations are inaccurate, and (f) male wasps sometimes disperse. These data and calculations suggest that alternative explanations must be considered seriously. Substantial data show that wasps typically lay most of their male eggs first followed by mostly female eggs require a new approach. These “slope” strategies result in more accurate sex ratios that are automatically adjusted to foundress number, own and relative clutch sizes and to sequential clutches. This effect will alter sex ratios in all species once the egg capacity of a fig is crossed or when interference reduces clutch sizes. In addition to this passive response, the females of about half the studied species have a conditional response that reduces female bias under higher foundress numbers by laying more sons. Therefore, wasps seem to use a very simple strategy that increases their fitness. Natural selection could have optimized parameters of the slope strategy and possibly the existence of the slope strategy itself. Variation in the slope strategy that is the result of natural selection is adaptive. Research should therefore focus on quantifying variables of this slope strategy. Currently, it is unclear how much of the variation is adaptive as opposed to being coincidental by-products. Graphical Abstract

The significant role of post-pairing male behavior on the evolution of male preferences and female traits

Existing sexual selection theory postulates that a sufficiently large variation in female fecundity or other direct benefits are fundamental for generating male mate choice. In this study, we suggest that, in addition to pre-pairing preferences, choosy males can also have different post-pairing behaviors, a factor which has been comparatively overlooked by previous studies. We found that both male preferences and female traits could evolve much more easily than previously expected when the choosy males that paired with unpreferred females would allocate more efforts to seeking additional post-pairing mating opportunities. Furthermore, a costly female trait could evolve when there was a trade-off between seeking additional mating and paternal care investment within social pair for choosy males. Finally, a costly male preference and a costly female trait might still evolve and reach a stable polymorphic state in the population, which might give rise to a high variability in male choice and female traits in nature. We suggest that male mate choice may be even more common than expected, which needs to be verified empirically.

Size-structured mating niche differentiation in the male-polyphenic mite Rhizoglyphus robini

Condition-dependent expression of alternative male morphs evolves when males of different sizes experience different mating niches, requiring different morphologies. Such mating niche differentiation can be due to competitive asymmetry between large and small males in contests over mating opportunities. Here, we tested the hypothesis that aggressive interactions among males cause size-structured mating niches in an acarid mite with condition-dependent male polyphenism: the bulb mite Rhizoglyphus robini. In this species, large males mature as armed fighters with enlarged legs, and small males as scramblers without modified legs. We staged experimental dyadic contests over a mating opportunity between either a pair of fighter males, or a fighter and a scrambler male. We predicted that the larger male would have a higher likelihood of mating first in contests among fighters, that the fighter male would have a higher likelihood of mating first in fighter-scrambler contests, that fighters would have a higher likelihood of interrupting ongoing copulations if they are larger than their mating rival, and that copulations in the presence of a fighter rival therefore last shorter than copulations with a scrambler rival present. We found that in contests among fighters, the larger male had a higher probability of mating first. In contests among a fighter and scrambler, the fighter male was more likely to mate first regardless of the body size difference between the contestants. Ongoing copulations were only rarely interrupted by the rival male (always by a fighter), and the probability of interruption did not depend on the body size difference between the mating male and its rival. Copulations lasted shorter in the presence of a rival fighter, but this effect was not attributable to interruption of copulations. We conclude that the fighting niche is particularly accessible for large males, as larger males have a higher probability of winning pre-copulatory contests. Such mating niche differentiation likely contributes to evolutionary maintenance of condition-dependent male polyphenism, where small males are forced to adopt an alternative mating tactic and hence develop a dedicated morphology.

The Evolution of Competition

Human competition is, at least partially, responsible for some of the transcended achievements of the species (walking on the moon, the polio vaccine, etc.), but the forces unleashed by competition have also led to profound human suffering (warfare, domination of one group by another group, etc.). In this article, the authors approach competition from an evolutionary perspective, applying Darwin’s theories of natural and sexual selection to understand better the nature of human competition. From the perspective of evolutionary psychology, humans engage in competition to gain resources, including status, food, and mating opportunities. Males tend to engage in more overt and aggressive forms of competition than females, but both sexes desire access to material and cultural goods associated with reproductive fitness. In the last roughly seventy years, the nature of men’s competition has transformed dramatically leading to declines in both within and between-group violence. As developed societies have succeeded in suppressing more overt and destructive forms of male–male competition, men attempt to gain status through occupational success, cognitive sophistication, moral signaling, and other relatively nonviolent behaviors. In this sense, men’s and women’s competition is more similar than it was a century ago. However, women’s competition is still less visible and relies on more indirect mechanisms (e.g., spreading gossip, subtle use of body language). For this reason, female–female competition has attracted less study than male–male competition. Fortunately, in the last decade, psychologists have partially redressed this imbalance.

Chicken gut microbiome members limit the spread of an antimicrobial resistance plasmid in Escherichia coli

Plasmid-mediated antimicrobial resistance is a major contributor to the spread of resistance genes within bacterial communities. Successful plasmid spread depends upon a balance between plasmid fitness effects on the host and rates of horizontal transmission. While these key parameters are readily quantified in vitro , the influence of interactions with other microbiome members is largely unknown. Here, we investigated the influence of three genera of lactic acid bacteria (LAB) derived from the chicken gastrointestinal microbiome on the spread of an epidemic narrow-range ESBL resistance plasmid, IncI1 carrying bla CTX-M-1 , in mixed cultures of isogenic Escherichia coli strains. Secreted products of LAB decreased E. coli growth rates in a genus-specific manner but did not affect plasmid transfer rates. Importantly, we quantified plasmid transfer rates by controlling for density-dependent mating opportunities. Parametrization of a mathematical model with our in vitro estimates illustrated that small fitness costs of plasmid carriage may tip the balance towards plasmid loss under growth conditions in the gastrointestinal tract. This work shows that microbial interactions can influence plasmid success and provides an experimental-theoretical framework for further study of plasmid transfer in a microbiome context.

Pelt Biting as a Practical Indicator of Social and Environment Stress in Farmed Red Deer

Agonistic behavioural interactions play a decisive role in the competition for food, space, mating opportunities, and establishing social rank. We used pelt biting (number of bites on an animal’s body) as a proxy for assessing the intensity of agonistic animal interactions and how it responded to social, population, and heat stress factors. We modelled a 14-year time series of pelt biting records and observational data of agonistic interactions on a population of captive Iberian red deer (Cervus elaphus). We found that (i) the higher the social rank of deer, the lower the number of pelt bites received; (ii) increasing heat stress conditions caused deer to suffer more pelt bites; (iii) males received more bites than females; (iv) the heavier the deer, the lower the number of bites on their bodies; (v) the bigger the group, the more bites exhibited on its members; (vi) deer 5–6 years old suffered greater rate of pelt biting than younger or older deer; and (vii) hinds that gave birth earlier in the parturition period suffered less pelt biting than those that gave birth around the peak of the parturition season (p < 0.01 for all effects). Pelt biting is useful to predict management situations in which deer welfare could be at stake.

Intraspecific Competition, Habitat Quality, Niche Partitioning, and Causes of Intrasexual Territoriality for a Reintroduced Carnivoran

Animals exploring a new environment develop cognitive maps using diverse sensory input and, thereby, gain information needed to establish home ranges. Experiencing, and learning information about, resources should be advantageous to the resident of a home range while lack of such information should put invaders into the home range at a disadvantage. Conspecifics, especially, should avoid the home ranges of one another to ensure that they do not experience reduced resource availability caused by resource depression or depletion. Yet, encountering conspecific competitors of different sexes may elicit responses that can lead to spacing on a landscape that has different costs and benefits on males and females. We tested the hypothesis that female fishers (Pekania pennanti) avoid competition from both males and female conspecifics whereas male fishers avoid competition only from other males. We reintroduced fishers onto our study site in the presence or absence of competitors’ home ranges during late 2009 through 2011. Using satellite transmitters (Argos) and land-based (VHF) telemetry, we monitored fishers and estimated their locations, movements and use of the surrounding landscape during their first 500 days after release. All fishers settled in relatively high-quality habitat but females that encountered the home ranges of conspecifics moved farther, explored larger areas, and settled farther from their release locations than did females that did not encounter a conspecific’s home range. Male fishers exhibited diverse responses upon encountering the home ranges of conspecifics. Thus, female fishers avoid conspecific competition from all fishers, but males tolerate, or impose, competition with females, apparently to increase mating opportunities. These observations are consistent with the movements and strategies of other solitary carnivores.

Against the Odds: Hybrid Zones between Mangrove Killifish Species with Different Mating Systems

Different mating systems are expected to affect the extent and direction of hybridization. Due to the different levels of sexual conflict, the weak inbreeder/strong outbreeder (WISO) hypothesis predicts that gametes from self-incompatible (SI) species should outcompete gametes from self-compatible (SC) ones. However, other factors such as timing of selfing and unilateral incompatibilities may also play a role on the direction of hybridization. In addition, differential mating opportunities provided by different mating systems are also expected to affect the direction of introgression in hybrid zones involving outcrossers and selfers. Here, we explored these hypotheses with a unique case of recent hybridization between two mangrove killifish species with different mating systems, Kryptolebias ocellatus (obligately outcrossing) and K. hermaphroditus (predominantly self-fertilizing) in two hybrid zones in southeast Brazil. Hybridization rates were relatively high (~20%), representing the first example of natural hybridization between species with different mating systems in vertebrates. All F1 individuals were sired by the selfing species. Backcrossing was small, but mostly asymmetrical with the SI parental species, suggesting pattern commonly observed in plant hybrid zones with different mating systems. Our findings shed light on how contrasting mating systems may affect the direction and extent of gene flow between sympatric species, ultimately affecting the evolution and maintenance of hybrid zones.

Evolutionary Perspectives on Maternal Parenting

This chapter focuses on maternal care, including the specialized psychological mechanisms designed to shape maternal solicitude and the various factors to which these mechanisms are sensitive. It identifies factors that influence levels of maternal parental investment. Maternal factors that lead to increased investment include the amount of resources available, potential for future mating opportunities and maternal age, and number of offspring. Child factors that lead to greater investment include reproductive value, age of the child, sex, offspring need, and relatedness to the mother. Although there has been an abundance of research on maternal parental investment, most of the studies have focused on individual factors that influence parental investment levels with only a few investigating interactive models. Therefore, more research investigating interactive models is necessary to better understand under which circumstances mothers would be more or less likely to invest in their offspring.

Sexual selection on population-level mating opportunities drives morph ratios in a fig wasp with extreme male dimorphism

Background Alternative mating tactics are widespread in animals and associated with extreme morphological polymorphism in some insects. Some fig wasps have both highly modified wingless males and dispersing winged males. Wingless males mate inside figs before females disperse, while winged males mate elsewhere after dispersal. Hamilton proposed a model for this system with morphs determined by alternative alleles. This has an equilibrium where the proportion of winged males equals the proportion of females dispersing unmated; i.e. the proportion of matings that they obtain. Previously, we have shown qualitative support for this prediction across nine wing-dimorphic fig wasp species. Here I test the quantitative prediction in the fig wasp Pseudidarnes minerva. In addition, some fig wasp species that lack winged males, but have two wingless morphs, show a conditional strategy with morph determination influenced by the number of wasps developing in a patch. I also test for this alternative pattern in the wing-dimorphic P. minerva. Results I sampled 114 figs that contained a mean of 2.1 P. minerva wasps from 44 trees across four sites in Sydney, Australia. At the whole population level, the proportion of winged males (0.84 or 0.79 corrected for sampling bias) did not differ significantly from the proportion of unmated females (0.84), providing strong quantitative support for the prediction of Hamilton’s model. In addition, there was no evidence for other factors, such as local mate competition or fighting between wingless males, that could violate simplifying assumptions of the model. Meanwhile, the proportion of winged males was not correlated with the number of wasps per fig, providing no evidence for a conditional strategy. Conclusion The morph ratio in P. minerva is consistent with Hamilton’s simple Mendelian strategy model, where morph ratios are set by average mating opportunities at the population level. This contrasts with some fig wasps from another subfamily that show conditional morph determination, allowing finer scale adaptation to fig-level mating opportunities. However, these conditional cases do not involve wing polymorphism. Male polymorphism is common and variable in fig wasps and has evolved independently in multiple lineages with apparently different underlying mechanisms.