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.

Male Age Influences Re-mating Incidence and Sperm Use in Females of the Dengue Vector Aedes aegypti

Diseases transmitted by female Aedes aegypti mosquitoes are public health issues in countries in the tropics and sub-tropics. As in other insects, A. aegypti females undergo behavioral and physiological changes upon mating that principally act to facilitate the production of progeny. The primary effectors of A. aegypti female post-mating responses are male-derived seminal proteins that are transferred to females during mating. Increased male age reduces ejaculate function in numerous taxa and alters seminal protein composition in Drosophila melanogaster, but the impacts of male age on female A. aegypti post-mating responses are unknown. Here, we used “old” (21–22 days old) and “young” (4–5 days old) A. aegypti males to assess the influence of male age on oviposition, fertility, and re-mating incidence in their mates. We also examined how age influenced paternity share in females initially mated to young or old males that subsequently re-mated with a transgenic male that transferred RFP-labeled sperm and whose progeny inherited a larval-expressed GFP marker. We found that increased male age had no effect on female fecundity or fertility but significantly impacted their ability to prevent re-mating in their mates—more than half (54.5%) of the females mated to an old male re-mated, compared to 24% of females initially mated to a young male. Polyandrous A. aegypti females displayed first male precedence regardless of the age of their initial mate. However, young males were better able to compete with rival male sperm, siring significantly more progeny (77%) compared to old males (64%). Young males had significantly more sperm in their seminal vesicles than old males at the time of mating, although males of both age groups transferred similar numbers of sperm to their mates. Our results suggest that male senescence differentially impacts the induction of some post-mating changes in A. aegypti females. As the effect of age may be further exacerbated in the field, age-related declines in male ability to induce sexual refractoriness have implications for A. aegypti population control programs that release adults into the environment.

The influence of male dominance in female Anastrepha curvicauda mate selection

Males of the papaya fruit fly, Anastrepha curvicauda Gerstaecker (former Toxotrypana curvicauda), defend a papaya fruit from rivals and males release their sex pheromone to attract and mate with females and offer them an oviposition site. While some aspects of the biology of A. curvicauda are known, such as its reproductive biology, its sex pheromone, and host selection, there is currently no information on the species mate selection process. This paper describes the precopulatory mating behavior of A. curvicauda and elucidates how intrasexual selection affects the mate selection process. We studied the precopulatory mating behavior of dominant and subordinate males and ethograms were devised. The effect of hierarchy was studied in non-choice and choice experiments. Male’s repertoire includes 15 behavioral elements, 12 precopulatory, one mating, and two postcopulatory (tandem and encounter). In non-choice experiments, dominant and subordinate males were accepted by females, but when females had the opportunity to choose among males, dominant males were significantly preferred over subordinate ones. The presence of a rival male modified the courting behavior of males and agonistic behavior among males was observed before and during mating.

Flexible memory controls sperm competition responses in male Drosophila melanogaster

Males of many species use social cues to predict sperm competition (SC) and tailor their reproductive strategies, such as ejaculate or behavioural investment, accordingly. While these plastic strategies are widespread, the underlying mechanisms remain largely unknown. Plastic behaviour requires individuals to learn and memorize cues associated with environmental change before using this experience to modify behaviour. Drosophila melanogaster respond to an increase in SC threat by extending mating duration after exposure to a rival male. This behaviour shows lag times between environmental change and behavioural response suggestive of acquisition and loss of memory. Considering olfaction is important for a male's ability to assess the SC environment, we hypothesized that an olfactory learning and memory pathway may play a key role in controlling this plastic behaviour. We assessed the role of genes and brain structures known to be involved in learning and memory. We show that SC responses depend on anaesthesia-sensitive memory, specifically the genes rut and amn . We also show that the γ lobes of the mushroom bodies are integral to the control of plastic mating behaviour. These results reveal the genetic and neural properties required for reacting to changes in the SC environment.

Conflict between background matching and social signalling in a colour-changing freshwater fish

The ability to change coloration allows animals to modify their patterning to suit a specific function. Many freshwater fishes, for example, can appear cryptic by altering the dispersion of melanin pigment in the skin to match the visual background. However, melanin-based pigments are also used to signal dominance among competing males; thus colour change for background matching may conflict with colour change for social status signalling. We used a colour-changing freshwater fish to investigate whether colour change for background matching influenced aggressive interactions between rival males. Subordinate males that had recently darkened their skin for background matching received heightened aggression from dominant males, relative to males whose coloration had not changed. We then determined whether the social status of a rival male, the focal male's previous social status, and his previous skin coloration, affected a male's ability to change colour for background matching. Social status influenced skin darkening in the first social encounter, with dominant males darkening more than subordinate males, but there was no effect of social status on colour change in the second social encounter. We also found that the extent of skin colour change (by both dominant and subordinate males) was dependent on previous skin coloration, with dark males displaying a smaller change in coloration than pale males. Our findings suggest that skin darkening for background matching imposes a significant social cost on subordinate males in terms of increased aggression. We also suggest that the use of melanin-based signals during social encounters can impede subsequent changes in skin coloration for other functions, such as skin darkening for background matching.

Behavioural induction of unreceptivity to mating from a post-copulatory display in the red mason bee, Osmia bicornis

In monandrous species, females have to manage their mating receptivity not only to gather an appropriate sperm supply, but to avoid further male sexual harassment as well. The shutdown of female receptivity to mating is often an irreversible process and therefore should result from a reliable signal. Females of the red mason bee, Osmia bicornis (syn. O. rufa), mate only once within the first day after their emergence from the maternal nest. The unreceptivity to mating of a mated female is induced by a male post-copulatory display, which takes place for about 10 min after ejaculating. During this display the male obviously applies an anti-aphrodisiac that reduces female’s attractiveness resulting in protection from other rival male sexual harassment. Protection by odour is only temporarily needed because females eventually reduce their attractiveness and receptivity to mating by themselves within a few days after emergence. The autonomous decrease in virgin female’s receptivity to mating is simply age driven and independent from mating status. In summary, the involvement of ejaculate substances in causing a loss of female receptivity to mating can be excluded for this species.

Male–male competition leads to less abundant but more attractive sperm

Males employ complex strategies to optimize their reproductive success when faced with male–male competition; for instance, they can adjust the ejaculate characteristics. In copulating species, a male may also strategically adjust his ejaculate expenditure according to female quality. Quantifying the relative contribution of ejaculate plasticity in male reproductive success is often difficult, especially when females exert postcopulatory cryptic choice. One way to quantify the functional significance of ejaculate plasticity is offered by mating systems in which the reproductive partners do not meet each other during insemination. In the collembolan Orchesella cincta , males deposit their ejaculates (spermatophores) irrespective of the presence of females. We tested whether Orchesella males adjust spermatophore number when exposed to the presence of another male and whether changes in spermatophore production influence female choice. We found that Orchesella males display plasticity in spermatophore allocation. Males decreased the spermatophore number when exposed to a rival male. Moreover, females preferentially took up spermatophores of males that were exposed to a competitor. The reduction in spermatophore number suggests, besides an adaptive response to the risk of ejaculate removal by rival males, an optimization strategy owing to the costs of more attractive spermatophores.