Introduced ants (Hymenoptera: Formicidae) of mainland France and Belgium,with a focus on greenhouses

The monitoring of introduced species is becoming more important as global trade intensifies. Although ants make up a larger proportion of species on the list of the most invasive species in the world compared with other groups, little is known about the occurrence of those introduced in France, especially inside heated buildings. Here we review the literature available for mainland France and Belgium and report the results of a survey conducted with the help of tropical building managers between 2014 and 2016. We report for the first time in France the presence of Technomyrmex vitiensis and Plagiolepis alluaudi in multiple greenhouses. Technomyrmex difficilis was also found in one greenhouse for the first time in Europe. The diversity of introduced ants in greenhouses is very low, and these buildings are most often dominated by one or two species. We compared the most recent data and those collected throughout the twentieth century and showed that ant communities have changed substantially. Greenhouses could be responsible for the introduction of invasive species because they regularly import exotic plants, but we found no evidence that the three species of invasive ants present outdoors in France were introduced from greenhouses, where they rarely occur. We also report that introduced ants are pests in greenhouses because they disperse scale insects and kill biological control agents. The suppression of these ants could ease the maintenance of plants inside greenhouses.     

Permanent Genetic Resources added to Molecular Ecology Resources Database 1 February 2013–31 March 2013

This article documents the addition of 142 microsatellite marker loci to the Molecular Ecology Resources database. Loci were developed for the following species: Agriophyllum squarrosum, Amazilia cyanocephala, Batillaria attramentaria, Fungal strain CTeY1 (Ascomycota), Gadopsis marmoratus, Juniperus phoenicea subsp. turbinata, Liriomyza sativae, Lupinus polyphyllus, Metschnikowia reukaufii, Puccinia striiformis and Xylocopa grisescens. These loci were cross‐tested on the following species: Amazilia beryllina, Amazilia candida, Amazilia rutila, Amazilia tzacatl, Amazilia violiceps, Amazilia yucatanensis, Campylopterus curvipennis, Cynanthus sordidus, Hylocharis leucotis, Juniperus brevifolia, Juniperus cedrus, Juniperus osteosperma, Juniperus oxycedrus, Juniperus thurifera, Liriomyza bryoniae, Liriomyza chinensis, Liriomyza huidobrensis and Liriomyza trifolii.     

The Evolution of Communication in Two Ant-Plant Mutualisms

Myrmecophytes are plants that provide nesting sites and food to ants that protect them against herbivores. Plant signals function to synchronize ant patrolling with the probability of herbivory. We compared the communication signals in two symbioses involving ant and plant pairs that are closely related. The two plants emitted the same volatile compounds upon damage. These compounds are simple molecules common in the plant kingdom. Electroantennography revealed that the two symbiotic ants, as well as several other ant species, were able to perceive these compounds. However, workers of one species responded only to hexanal, while those of the other species responded mostly to methyl salicylate. The two signals involved in the focal symbioses are ‘cheap’ (low metabolic cost), which is consistent with theoretical predictions for the evolution of signalling between partners with convergent interests. They are also not specific, which is expected between plants and broad-spectrum predators such as ants. The fact that different signals are used in the two sister symbioses suggests different mechanisms underlying similar adaptations in the evolution of communication.