Morphological structures used as weapons in male–male competition are not only costly to develop but are also probably costly to maintain during adulthood. Therefore, having weapons could reduce the energy available for other fitness‐enhancing actions, such as post‐copulatory investment. We tested the hypothesis that armed males make lower post‐copulatory investments than unarmed males, and that this difference will be most pronounced under food‐limited conditions. We performed two experiments using the male‐dimorphic bulb mite Rhizoglyphus robini, in which males are either armed “fighters” or unarmed “scramblers.” Firstly, we tested whether fighters and scramblers differed in their reproductive output after being starved or fed for 1 or 2 weeks. Secondly, we measured the reproductive output of scramblers and fighters (starved or fed) after one, two or three consecutive matings. Scramblers sired more offspring than fighters after 1 week, but scramblers and fighters only sired a few offspring after 2 weeks. Scramblers also sired more offspring than fighters at the first mating, and males rarely sired offspring after consecutive matings. Contrary to our hypothesis, the fecundity of starved and fed males did not differ. The higher reproductive output of scramblers suggests that, regardless of nutritional state, scramblers make larger post‐copulatory investments than fighters. Alternatively, (cryptic) female choice generally favours scramblers. Why the morphs differed in their reproductive output is unclear. Neither morph performed well relatively late in life or after multiple matings. It remains to be investigated to what extent the apparent scrambler advantage contributes to the maintenance and evolution of male morph expression.
In male-dimorphic species, males are often either armoured 'majors' that can monopolise access to females, or unarmoured and defenceless 'minors' that cannot. However, majors, unlike minors, have to spend energy to maintain their weaponry. Like-for-like, this could mean that minors have relatively more energy available to increase their reproductive output through e.g. sperm competition, or the transference of nutrients by means of a nuptial gift. Such a fitness advantage to minors could therefore contribute to explaining the coexistence of both morphs in single populations. We tested if food-deprived females of the male-dimorphic bulb mite Rhizoglyphus robini produced more eggs when mated to a minor or to a major male, and whether egg production depended on whether their mates were starved or fed prior to mating. We found no effect of male morph on female fecundity, but females did produce more eggs when mated to previously fed males. We also found that females increased in mass, but males decreased in mass over the course of the experiment. From these observations we infer that fed males are able to transfer nutrients, a nuptial gift, to their mate. This is the first observation to suggest nuptial gift transfer in mites. Though males of both morphs appeared able to produce nuptial gifts; other factors, like habitat complexity, should be considered to identify fitness benefits of minor over major males to understand why the two morphs coexist.
In haplodiploid organisms including the two-spotted spider mite, Tetranychus urticae (Acari: Tetranychidae), both unmated and mated females can produce male offspring. A previous study reported that males produced by unmated females (UM males) find pre-reproductive females more quickly than males produced by mated females (M males) in T. urticae. However, it remains unclear what factors cause the difference. We investigated effects of maternal mating status on mate-searching behaviour of their sons by changing the sons’ developmental environment. In T. urticae, the primary sex ratio of mated-female colonies is female-biased. For both UM and M males, half of individuals were reared with males to imitate unmated-female colonies, whereas the rest were reared with females to imitate mated-female colonies. In UM males, individuals that had developed with males found pre-reproductive females more quickly than those that had developed with females. However, such a difference was not observed in M males. This indicates that behavioural response to the developmental environment differs between UM and M males. It means that the behavioural plasticity depends on maternal mating status. When males were individually reared, however, there was no significant difference in the mate-searching behaviour between UM and M males, indicating that maternal mating status does not independently affect their sons’ mate-searching behaviour. This study showed that male mate-searching behaviour is changed by their developmental environment and maternal mating status. This behavioural plasticity depending on maternal mating status is the first reported in haplodiploid organisms.
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