Local adaptation is of fundamental interest to evolutionary biologists. Traditionally, local adaptation has been studied using reciprocal transplant experiments to quantify fitness differences between residents and immigrants in pairwise transplants between study populations. Previous studies have detected local adaptation in some cases, but others have shown lack of adaptation or even maladaptation. Recently, the importance of different fitness components, such as survival and fecundity, to local adaptation have been emphasized. Here, we address another neglected aspect in studies of local adaptation: sex differences. Given the ubiquity of sexual dimorphism in life histories and phenotypic traits, this neglect is surprising, but may be partly explained by differences in research traditions and terminology in the fields of local adaptation and sexual selection. Studies that investigate differences in mating success between resident and immigrants across populations tend to be framed in terms of reproductive and behavioural isolation, rather than local adaptation. We briefly review the published literature that bridges these areas and suggest that reciprocal transplant experiments could benefit from quantifying both male and female fitness components. Such a more integrative research approach could clarify the role of sex differences in the evolution of local adaptations.This article is part of the theme issue 'Linking local adaptation with the evolution of sex differences'.

The Asian giant hornet (AGH, Vespa mandarinia) is the world’s largest hornet, occurring naturally in the Indomalayan region, where it is a voracious predator of pollinating insects including honey bees. In September 2019, a nest of Asian giant hornets was detected outside of Vancouver, British Columbia; multiple individuals were detected in British Columbia and Washington state in 2020; and another nest was found and eradicated in Washington state in November 2020, indicating that the AGH may have successfully wintered in North America. Because hornets tend to spread rapidly and become pests, reliable estimates of the potential invasive range of V. mandarinia in North America are needed to assess likely human and economic impacts, and to guide future eradication attempts. Here, we assess climatic suitability for AGH in North America, and suggest that, without control, this species could establish populations across the Pacific Northwest and much of eastern North America. Predicted suitable areas for AGH in North America overlap broadly with areas where honey production is highest, as well as with species-rich areas for native bumble bees and stingless bees of the genus Melipona in Mexico, highlighting the economic and environmental necessity of controlling this nascent invasion.

While gene flow can reduce the potential for local adaptation, hybridization may conversely provide genetic variation that increases the potential for local adaptation. Hybridization may also affect adaptation through altering sexual dimorphism and sexual conflict, but this remains largely unstudied. Here, we discuss how hybridization may affect sexual dimorphism and conflict due to differential effects of hybridization on males and females, and then how this, in turn, may affect local adaptation. First, in species with heterochromatic sexes, the lower viability of the heterogametic sex in hybrids could shift the balance in sexual conflict. Second, sex-specific inheritance of the mitochondrial genome in hybrids may lead to cytonuclear mismatches, for example, in the form of 'mother's curse', with potential consequences for sex ratio and sex-specific expression. Third, sex-biased introgression and recombination may lead to sex-specific consequences of hybridization. Fourth, transgressive segregation of sexually antagonistic alleles could increase sexual dimorphism in hybrid populations. Sexual dimorphism can reduce sexual conflict and enhance intersexual niche partitioning, increasing the fitness of hybrids. Adaptive introgression of alleles reducing sexual conflict or enhancing intersexual niche partitioning may facilitate local adaptation, and could favour the colonization of novel habitats. We review these consequences of hybridization on sex differences and local adaptation, and discuss how their prevalence and importance could be tested empirically.This article is part of the theme issue 'Linking local adaptation with the evolution of sex differences'.

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Background Theory predicts that parasites can affect and thus drive their hosts’ niche. Testing this prediction is key, especially for vector-borne diseases including Chagas disease. Here, we examined the niche use of seven triatomine species that occur in Mexico, based on whether they are infected or not with Trypanosoma cruzi , the vectors and causative parasites of Chagas disease, respectively. Presence data for seven species of triatomines ( Triatoma barberi , T. dimidiata , T. longipennis , T. mazzottii , T. pallidipennis , T. phyllosoma and T. picturata ) were used and divided into populations infected and not infected by T. cruzi . Species distribution models were generated with Maxent 3.3.3k. Using distribution models, niche analysis tests of amplitude and distance to centroids were carried out for infected vs non-infected populations within species. Results Infected populations of bugs of six out of the seven triatomine species showed a reduced ecological space compared to non-infected populations. In all but one case ( T. pallidipennis ), the niche used by infected populations was close to the niche centroid of its insect host. Conclusions Trypanosoma cruzi may have selected for a restricted niche amplitude in triatomines, although we are unaware of the underlying reasons. Possibly the fact that T. cruzi infection bears a fitness cost for triatomines is what narrows the niche breadth of the insects. Our results imply that Chagas control programmes should consider whether bugs are infected in models of triatomine distribution. Electronic supplementary material The online version of this article (10.1186/s13071-019-3489-5) contains supplementary material, which is available to authorized users.

Ornaments may show hyperallometry in certain taxa, i.e. large individuals have proportionally larger ornaments than small ones. One hypothesis suggests that higher sexual selection intensity leads to steeper hyperallometric patterns. This study tested whether an ornamental trait subject to both intra‐ and intersexual selection showed steeper allometric slopes than when subject solely to intrasexual selection. The study employed the sexually selected male wing pigmentation of 14 calopterygid species (damselflies) that differ in sexual selection intensity (intrasexual selection versus intra‐ and intersexual selection). Hyperallometry was not a uniform pattern in the study species. Furthermore, the allometric slopes did not differ between sexual selection intensities. The allometry of ornamental traits is therefore highly variable even among related species. Other selection pressures – probably species‐specific and at a local scale – acting on wing pigmentation might explain the diversity of allometric patterns.

Male abdominal grasping apparatus that are used to secure a female prior, during and after mating, are widespread in arthropods. The scarce evidence regarding its selective regime suggests that they are male adaptations to circumvent female mating decisions, as predicted by the sexual conflict hypothesis. A recent discussion regarding this way of selection suggests that, similar to weapons and traits that have to do with physical endurance, grasping apparatus should show hyperallometry (proportionally larger compared to body size) as an indication of selection towards increased size. We have tested this idea by measuring the length, width and area of the grasping apparatus of five dragonfly species (Anax junius, Rhionaeschna multicolor, Dythemis nigrescens, D. sterilis and Phyllogomphoides pacificus). We used two proxies of body size (wing and body length). Our measures did not indicate any pattern of hyperallometry. Thus, the grasping apparatus in these animals does not seem to be positively selected for increased size as would be expected if they were forcing females to mate. Given this, we discuss three other explanations for the maintenance of the grasping apparatus in odonates: 1) a firm grip that secures the tandem and mating position; 2) courtship devices subject to female choice; and, 3) isolation structures that mechanically prevent interspecific matings. The first hypothesis, however, could not J Insect Behav (2015) 28:15-25 explain the highly elaborated and species specific morphology of grasping apparatus in these animals. Support for the second hypothesis comes from the fact that odonate females have mechanoreceptor sensilla embedded in their mesostigmal plates (the place grabbed by the grasping apparatus). For the third hypothesis, coevolutionary patterns in morphology in the grasping apparatus and mesostigmal plates in some Zygoptera can also be used as support.

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