Wedged between bottom-up and top-down processes: aphids on tansy

Abstract. 1. Many species of aphids exploit a single host‐plant species and have to cope with changing environmental conditions. They often vary greatly in abundance even when feeding on the same host. In a field experiment, the bottom‐up (plant quality/patch type frequency) and top‐down (ant attendance/predation) effects on the abundance of four species of aphids feeding on tansy (Tanacetum vulgare) were tested using a full factorial design. In addition, a model was used to examine these patch characteristics for their relative effects on the population dynamics and abundance of different aphid species. 2. Aphid numbers changed significantly depending on the quality of the host plant and the presence/absence of attending ants. The obligate myrmecophile, Metopeurum fuscoviride, was abundant on high‐quality plants, while on poor quality plants or on plants without attending ants these aphids did not survive until the end of the experiment. The facultative myrmecophiles, Aphis fabae and Brachycaudus cardui, and the unattended aphid species, Macrosiphoniella tanacetaria, all reached similar peak population densities, but M. tanacetaria did best in poor quality patches. 3. Natural enemies reduced aphid numbers, but those species feeding on high‐quality plants survived longer than those on poor‐quality plants, which existed only for a short period of time, especially when associated with ants. Losses due to migration of winged morphs and mortality caused by parasitoids were insignificant. 4. Varying the frequency of different patch types in a model indicates that different degrees of associations with ants are favoured in different environments. If the proportion of high‐quality patches in a habitat is large, obligate myrmecophiles do best. On increasing the number of poor‐quality patches, unattended species become more abundant. 5. The results suggest that, in spite of large species specific differences in growth rates, degree of myrmecophily or life cycle features, the temporal and spatial variability in top‐down and bottom‐up forces differentially affects aphid species and allows the simultaneous exploitation of a shared host‐plant species.     

Of crazy-ants and Curetinae: are Curetis butterflies tended by ants?

The larvae of the lycaenid subfamily Curetinae have never been reported to be associated with ants. Observations on Curetis regula Evans from Brunei are presented which show that this species may be tended by ants both as larvae and adults. The observations are discussed in relation to a recent review on lycaenid/ant associations, u is suggested that the Curetinae will be found to be associated with ants when more species have been reared, on evidence of the larval tentacle organs and apparent 'pore cupolas', both of which are ant adaptations. More studies are needed on Curetis biology and larval morphology to resolve the relationships of this enigmatic genus within the Lycaenidae.     

Symbiont choice in a fungus-growing ant (Attini, Formicidae)

Cultivars of fungus-growing (attine) ants are vertically transmittedthrough inheritance from parent to offspring nest, but horizontalcultivar transfer between ant nests occurs occasionally, resultingin cultivar replacement within ant lineages. Two mechanismscould theoretically prevent the invasion of suboptimal cultivarstrains and thus stabilize ant–cultivar coevolution: first,partner feedback inherent in vertical cultivar transmissionand second, partner (symbiont) choice if the ants differentiatebetween productive and inferior cultivars during replacements.To elucidate the nature of symbiont choice, we presented workersof Cyphomyrmex muelleri with novel cultivars representing aphylogenetic cline of close and distant relatives of the nativeC. muelleri cultivar. Workers invariably preferred their nativecultivar, discriminating against even very close relatives ofthe native cultivar. When given a choice between two non-nativecultivar strains, workers accepted the strain most closely relatedto their native cultivar. Two conclusions emerge. First, colonyswitches to distantly related cultivars are behaviorally unlikelyand may not be preference-based; rather, distant switches mayoccur under constrained choice, such as pathogen-related gardenlosses that force colonies to import novel cultivars. Second,the ability of attine ants to differentiate between closelyrelated cultivar strains suggests that the ant–fungusmutualism is stabilized evolutionarily not only by partner feedbackinherent in vertical cultivar transmission, but possibly alsoby symbiont choice through which the ants select against unwanted,presumably inferior, cultivars. The efficacy of symbiont choicenow needs to be tested experimentally. Such research may benefitfrom application of theory and experimental paradigms that havebeen developed within the areas of mate choice and sexual selection.     

Effect of the Argentine ant on the specialist myrmecophilous cricket Myrmecophilus kubotai in western Japan

Effects of the Argentine ant on myrmecophilous animals living inside ant nests have been rarely studied to date. We investigated whether the “specialist” myrmecophilous cricket Myrmecophilus kubotai Maruyama that lives only in colonies of a Japanese native ant, Tetramorium tsushimae Emery, could live with the Argentine ant. In the field, the cricket was never found in nests of the Argentine ant. Our experiments showed that the cricket could not survive in artifical nests of the Argentine ant under laboratory conditions.     

The microsporidian pathogen Myrmecomorba nylanderiae: Intracolony transmission and impact upon tawny crazy ant (Nylanderia fulva) colonies

The microsporidian pathogen Myrmecomorba nylanderiae Plowes et al. infects introduced tawny crazy ants (Nylanderia fulva (Mayr)), and constitutes one of the first natural enemies known to attack this invasive ant. We assess how infection is transmitted within colonies and how infection impacts N. fulva colony fragment growth under carbohydrate‐deficient and carbohydrate‐sufficient dietary conditions. Carbohydrate scarcity is a common source of stress for ant colonies. Infected workers efficiently pass infection to developing larvae but all other potential pathways for within colony transmission are rare or non‐viable. For unknown reasons, queens within infected colony fragments are generally uninfected, limiting the role of transovarial transmission in intracolony transmission. In the laboratory, infection by M. nylanderiae primarily impacts the growth of N. fulva colonies by reducing pupal production. Colony growth showed a substantially greater impact under carbohydrate‐deficient conditions implying that the effect of the pathogen may depend on seasonally variable carbohydrate availability. In the colony growth assay, worker mortality did not differ with infection status under either nutrient regime. However, in a longer, direct test of survivorship, infected worker survivorship was significantly lower. Recently, some established N. fulva populations with high prevalence of M. nylanderiae infection have declined precipitously, though it is unknown if M. nylanderiae is a causative agent in these declines. The combination of chronic impacts, presence in North America, and potential association with population declines makes M. nylanderiae a promising prospect for the biological control of N. fulva.     

A duration constant for worker-to-larva trophallaxis in fire ants

Summary The allocation of liquid food by workers to larvae, a central process in ant biology, could be regulated by the frequency of trophallaxis, its duration, or both. In 4th-instar fire ant larvae, the duration of trophallaxis, bolus size, and the rate at which boluses were swallowed were all constant, indicating that the volume of food ingested during each worker-larva trophallaxis was both small and constant. Neither larval size over a 20-fold volume range nor larval starvation had a significant effect on duration of trophallaxis (mean = 11s, SD = 2s), bolus swallowing rate (mean = 2/s, SD = 0.5/s), or bolus volume (mean = 0.0675 nl, SD = 0.0002 nl, based on the assumption that the stomodaeum's epithelial layer is not expandable). Larval body orientation and larval location within the brood pile also had no effect on duration. Durations of trophallaxis by workers of different sizes were similar. Durations of trophallaxis for 1st-, 2nd-, and 3rd-instar worker larvae were also constant but greater than that for 4th-instar worker larvae. Fourth-instar minim larvae (from founding colonies) and 4th-instar worker larvae (from mature colonies) were fed for the same duration by workers but for different durations by founding queens. Founding queens fed minim larvae longer than they fed worker larvae. The durations of feedings to 4th-instar sexual larvae were more variable than those to worker larvae. Altogether, these findings indicated that 4th-instar worker larvae ingested a small, nearly constant volume of food (mean = 1.50 nl, SD = 0.005 nl) during each trophallactic event. Consequently, the long-term allocation of liquid food by workers to these larvae is regulated by the frequency of trophallaxis. Several other ant species showed a similar brevity and constancy in the duration of worker-larva trophallaxis. This brevity of worker-larva trophallaxis is in contrast to the duration of worker-worker trophallaxis.Although the duration of worker-larva trophallaxis appears to be determined by the worker, the data are not totally consistent with this interpretation.