We are proposing that the "relative" abundances of the differently tuned pheromone-component-responsive olfactory receptor neurons (ORNs) on insect antennae are not a result of natural selection working to maximize absolute sensitivity to individual pheromone components. Rather, relative abundances are a result of specifically tuned sensillum-plus-ORN units having been selected to accurately transduce and report to the antennal lobe the maximal ranges of molecular flux imparted by each pheromone component in every plume strand. To not reach saturating stimulus flux levels from the most concentrated plume strands of a pheromone blend, the dendritic surface area of the ORN type that is tuned to the most abundant component of a pheromone blend is increased in dendritic diameter in order to express a greater number of major pheromone component-specific odorant receptors. The increased ability of these enlarged dendrite, major component-tuned ORNs to accurately report very high flux of its component results in a larger working range of stimulus flux able to be accurately transduced by that type of ORN. However, the larger dendrite size and possibly other high-flux adjustments in titers of pheromone-binding proteins and degrading enzymes cause a decrease in absolute sensitivity to lower flux levels of the major component in lower concentration strands of the pheromone blend. In order to restore the ability of the whole-antenna major pheromone component-specific channel to accurately report to its glomerulus the abundance of the major component in lower concentration strands, the number of major component ORNs over the entire antenna is adjusted upward, creating a greater proportion of major component-tuned ORNs than those tuned to minor components. Pheromone blend balance reported by the whole-antennal major and minor component channels in low plume-flux strands is now restored, and the relative fluxes of the 2 components occurring in both low- and high-flux strands are thereby accurately reported to the component-specific glomeruli. Thus, we suggest that the 2 phenomena, dendrite size and relative numbers of differentially tuned ORNs are linked, and both are related to wide disparities in molecular flux ranges occurring for the more abundant and less abundant components in the pheromone blend plume strands.
Adult spotted lanternflies, Lycorma delicatula, launch themselves into the wind from elevated locations such as trees, lamp posts, and buildings. Individuals fly in short, successive bouts along descending trajectories of between 10 and 50 m before landing, crawling upward on a new structure, and again launching upwind. The possible physiological limits to the durations of flight-bouts, if not constrained by their poor ability to generate lift, however, remain unknown. In this study, we observed the behavior of tethered spotted lanternflies known to be prone to flight-dispersing, and recorded the number and durations of their successive flight bouts. Additionally, we recorded the flight distances and durations of similar spotted lanternflies in the field that had spontaneously taken flight or had been manually launched. We found that tethered females can perform >20 successive bouts with only 1 min between bouts when flight durations were limited to 20 s/bout. Bouts averaged 97.9 ± 11.4 s when bout durations were unlimited, with some females flying bouts lasting >400 s. Females could quickly advance upwind a distance >3000 m if the bouts of~100 s each were performed in quick succession in the field. However, adults spontaneously taking flight in the field flew for an average of only~13 s and traveled an average of 29 m before landing on the ground or on nearby objects. This information is important to determine how far a locally dispersing adult can fly before finding a suitable host to finish feeding and attain reproductive maturity.
Three species of North American heliothine moths were used to determine the level at which interspecific female interference of male attraction to conspecific females occurs. We used live calling females of Heliothis virescens, H. subflexa, and Helicoverpa zea, as lures for conspecific males in a wind tunnel, and then placed heterospecific females on either side of the original species such that the plumes of the three females overlapped downwind. In nearly all combinations, in the presence of heterospecific females, fewer males flew upwind and contacted or courted the source than when only conspecific females were used in the same spatial arrangement. Males did not initiate upwind flight to solely heterospecific female arrangements. Our results show that the naturally emitted pheromone plumes from heterospecific females of these three species can interfere with the ability of females to attract conspecific males when multiple females are in close proximity. However, the fact that some males still located their calling, conspecific females attests to the ability of these male moths to discriminate point source odors by processing the conflicting information from interleaved strands of attractive and antagonistic odor filaments on a split-second basis.
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