Insect sensory systems are the subjects of different selective pressures that shape their morphology. In many species of the flesh fly subfamily Miltogramminae (Diptera: Sarcophagidae) that are kleptoparasitic on bees and wasps, females perch on objects close to the host nests and, once a returning host is detected, they follow it in flight at a fixed distance behind until reaching the nest. We hypothesized that such satellite (SAT) flight behaviour, which implies a finely coordinated trailing flight, is associated with an improved visual system, compared to species adopting other, non-satellite (NON-SAT) strategies. After looking at body size and common ancestry, we found that SAT species have a greater number of ommatidia and a greater eye surface area when compared to NON-SAT species. Ommatidium area is only affected by body size, suggesting that selection changes disproportionately (relative to body size variation) the number of ommatidia and as a consequence the eye area, instead of ommatidium size. SAT species also tend to have larger ocelli, but their role in host-finding was less clear. This suggests that SAT species may have a higher visual acuity by increasing ommatidia number, as well as better stability during flight and motion perception through larger ocelli. Interestingly, antennal length was significantly reduced in SAT species, and ommatidia number negatively correlated with antennal length. While this finding does not imply a selection pressure of improved antennal sensory system in species adopting NON-SAT strategies, it suggests an inverse resource (i.e. a single imaginal disc) allocation between eyes and antennae in this fly subfamily.
Despite growing interest in gut microbiomes of aculeate Hymenoptera, research so far focused on social bees, wasps and ants, whereas non-social taxa and their brood parasites have not received much attention. Brood parasitism however allows to distinguish between microbiome components horizontally transmitted by spill-over from the host with such inherited through vertical transmission by mothers. Here, we studied the bacterial gut microbiome of adults in seven aculeate species in four brood parasite-host systems: two bee-mutillid (host-parasitoid) systems, one halictid bee-cuckoo bee system and one wasp-chrysidid cuckoo wasp system. We addressed the following questions: 1) Do closely related species possess a more similar gut microbiome? 2) Do brood parasites share components of the microbiome with their host? 3) Do brood parasites have different diversity and specialization of microbiome communities compared with the hosts? Our results indicate that the bacterial gut microbiome of the studied taxa was species-specific, yet with a limited effect of host phylogenetic relatedness and a major contribution of shared microbes between hosts and parasites. However, contrasting patterns emerged between bee-parasite systems and the wasp-parasite system. We conclude that the gut microbiome in adult brood parasites is largely affected by their host-parasite relationships and the similarity of trophic food sources between hosts and parasites.
The vast majority of species of velvet ants (Hymenoptera: Aculeata: Mutillidae) are ectoparasitoids of immature stages of other aculeate Hymenoptera (bees, wasps and ants). Due to their cryptic, furtive behaviour at the host nesting sites, however, even basic information on their biology, like host use diversity, is still unknown for entire subfamilies, and the known information, scattered in over two centuries of published studies, is potentially hiding tendencies to host specialization across velvet ant lineages. In this review, based on 305 host associations spanning 132 species in 49 genera and 10 main lineages (tribes/subfamilies), we explored patterns of host use in velvet ants. Overall, 15 families and 29 subfamilies of Aculeata are listed as hosts of mutillids, with a strong predominance of Apoidea (bees and apoid wasps: 19 subfamilies and 82.3% of host records). A series of bipartite networks, multivariate analyses and calculations of different indices suggested possible patterns of specialization. Host taxonomic spectrum (number of subfamilies) of velvet ants was very variable and explained by variation in the number of host records. Instead, we found a great variation of network-based host specialization degree and host taxonomic distinctness that did not depend on the number of host records. Differences in host use patterns seemed apparent across mutillid tribes/subfamilies, among genera within several tribes/subfamilies, and to lesser extent within genera. Taxonomic host use variation seemed not dependent on phylogeny. Instead, it was likely driven by the exploitation of hosts with different ecological traits (nest type, larval diet and sociality). Thus, taxonomically more generalist lineages may use hosts that essentially share the same ecological profile. Interestingly, closely related mutillid lineages often show contrasting combinations of host ecological traits, particularly sociality and larval diet, with a more common preference for ground-nesting hosts across most lineages. This review may serve as a basis to test hypotheses for host use evolution in this fascinating family of parasitoids.
Although recognition using cuticular chemistry is important for host–parasite interactions within aculeate Hymenoptera, cuticular hydrocarbon (CHC) profiles of only a few host–parasite pairs were characterized and compared. One largely neglected family in this context is the Mutillidae (velvet ants), whose species are ectoparasitoids of bees and wasps. In our study, we characterized and compared the CHC profiles of five species of Mutillidae and seven host species. The CHC profile of velvet ants differed among species and included large proportions of n-alkanes and methyl-branched alkanes. Alkenes were much less abundant in the CHC profiles of three species of velvet ants compared with their hosts, while the other two species possess a much lower abundance of methyl-branched alkanes than their hosts. Both the number of peaks and compound diversity were generally higher in velvet ants compared with their hosts. Thus, CHC profiles of parasitoids did not show signs of mimicry when compared with their hosts. In dyadic encounters between one species of velvet ant and its host bee species, the parasitoid mainly avoided interacting, while aggression by the host was rare. Our results suggest that velvet ants did not evolve chemical mimicry, perhaps in accordance with their wide host spectrum which would limit chemical specialization. However, the reduction of alkenes in social bee-attacking species and the reduction of methyl-branched alkanes in social wasp-attacking species may favour host nest invasion, since these two CHC classes are known to be important in nestmate recognition for social bees and wasps, respectively. A larger, phylogeny-corrected comparison of Mutillidae and hosts may help clarifying the evolution of the CHC profile of these parasitoids.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.