Grapevine is a well-studied, economically relevant crop, whose associated bacteria could influence its organoleptic properties. In this study, the spatial and temporal dynamics of the bacterial communities associated with grapevine organs (leaves, flowers, grapes, and roots) and soils were characterized over two growing seasons to determine the influence of vine cultivar, edaphic parameters, vine developmental stage (dormancy, flowering, preharvest), and vineyard. Belowground bacterial communities differed significantly from those aboveground, and yet the communities associated with leaves, flowers, and grapes shared a greater proportion of taxa with soil communities than with each other, suggesting that soil may serve as a bacterial reservoir. A subset of soil microorganisms, including root colonizers significantly enriched in plant growth-promoting bacteria and related functional genes, were selected by the grapevine. In addition to plant selective pressure, the structure of soil and root microbiota was significantly influenced by soil pH and C:N ratio, and changes in leaf- and grape-associated microbiota were correlated with soil carbon and showed interannual variation even at small spatial scales. Diazotrophic bacteria, e.g., Rhizobiaceae and Bradyrhizobium spp., were significantly more abundant in soil samples and root samples of specific vineyards. Vine-associated microbial assemblages were influenced by myriad factors that shape their composition and structure, but the majority of organ-associated taxa originated in the soil, and their distribution reflected the influence of highly localized biogeographic factors and vineyard management.
House dust mites (Dermatophagoides pteronyssinus) are widespread in the furniture and mattresses of homes throughout Eurasia. Because human occupation induces wide diurnal fluctuations in temperature and relative humidity, the most favourable locations for mites change constantly and they must migrate repeatedly. Here, we triggered and studied mites migration movements to a new area. Mites migrated from a starting arena to a second arena through a diamond‐shaped corridor offering a choice between two branches of equal length. In this article, we show that local air dryness and a distant water source were both necessary to trigger collective migration. Males and nymphs had a higher probability of migration than larvae and females. When migrating, although both branches initially appeared to be chosen equally, most mites eventually ended up choosing one particular branch. When about 50 or more mites had passed, there was an obvious choice of branch. We used a modelling approach to show that these data support the hypothesis that mites lay an attractive trail that is reinforced by followers. Consequently, the consistency of the collective choice is higher as the number of migrants grows. This article is the first to observe dust mite migration as a collective phenomenon.
The spruce bark beetle, Ips typographus, is causing severe economic losses during epidemic phases triggered by droughts and/or windstorms. Sanitation felling and salvage logging are usually the most recommended strategies to limit the damages. However, any additional control method to limit the economic impact of an outbreak would be welcome. In this respect, the efficiency of pheromone trapping is still controversial or poorly documented. In this 2-year study (2020–2021), at the peak of a severe outbreak in Belgium, we quantified the wood volume and presence/absence of new attacks at 126 sites attacked during the previous year and within 100 m from the initial attack. Each site was randomly allocated to one of three treatments: (1) three crosstraps baited with pheromones, (2) one tree-trap baited with pheromones and treated with an insecticide and (3) control sites with no trapping device. The attacked trees of the previous year were all cut and removed before the start of the experiment and newly attacked trees were removed as they were detected. The trapping devices were only active during spring to target overwintering bark beetles that might have escaped the sanitation cuts and to limit the risk of attracting dispersing beetles from outside the patch during the summer. We found a strong decrease of the attacks relative to the previous year in all treatments, including the controls (more than 50% of the control sites had no new attacks). There was no relationship between the new attacks and the attacks of the previous year. In both years, new attacks were more frequent (presence/absence) in sites with crosstraps (95% Confidence Interval [56–84%] of the sites with new attacks) than in sites with a tree-trap (26–57% - p = 0.02) and to a lesser extent than in control sites (32–63%, p = 0.08). In 2020, the attacked volumes were slightly higher in sites with crosstraps (95% Confidence Interval [3.4–14.2 m³]) than in control sites (0.2–3.5 m³, p = 0.04) and no significant difference was found with tree-trap sites (1.1–6.2 m³, p = 0.38). In 2021, there were no significant differences between the volumes attacked in the control sites (1.8–9.4 m³), crosstraps sites (0.9–6.4 m³) and tree-trap sites (0–2.5 m³). Overall, we found no evidence in favor of the efficacy of pheromone trapping during spring to reduce economic damages at the local scale when combined with sanitation felling and during a severe outbreak. The use of baited crosstraps could even be hazardous as it seemed to increase the occurrence of new attacks probably by attracting bark beetles but failing to neutralize them.
New lineages can arise through mosaic evolution of conserved, ancestral traits, and newly evolved, derived traits. Unraveling the origin of molecular pathways underlying the evolution of adaptive traits is essential for understanding how new lineages emerge. Here, we investigated the evolutionary divergence of sex pheromone communication from moths (mostly nocturnal) to butterflies (mostly diurnal) that occurred ~98 million years ago. In moths, females typically emit pheromones to attract male mates, but in butterflies pheromones are produced by males, a chemical signal on which females largely base their mate choice. The molecular bases of sex pheromone communication are well understood in moths, but have remained virtually unexplored in butterflies. Using a combination of transcriptomics, real time qPCR, and phylogenetics, our results suggest that the butterfly Bicyclus anynana relies on some moth-specific gene families (reductases) and on more ancestral insect gene families (desaturases, olfactory receptors, odorant binding proteins) for the biosynthesis and reception of sex pheromones. Interestingly, B. anynana further appears to use what was believed to be the moth-specific neuropeptide Pheromone Biosynthesis Activating Neuropeptide (PBAN) for sex pheromone regulation. Altogether, our results suggest that a mosaic pattern best explains how sex pheromone communication evolved in butterflies, with some molecular components derived from moths, and others conserved from more ancient insect ancestors. This is the first large-scale analysis of the genetic pathways underlying sex pheromone communication in a butterfly.
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