SUMMARY Visual identification of targets is an important task for many animals searching for prey or conspecifics. Dragonflies utilize specialized optics in the dorsal acute zone, accompanied by higher-order visual neurons in the lobula complex, and descending neural pathways tuned to the motion of small targets. While recent studies describe the physiology of insect small target motion detector (STMD) neurons, little is known about the mechanisms that underlie their exquisite sensitivity to target motion. Lobula plate tangential cells (LPTCs), a group of neurons in dipteran flies selective for wide-field motion, have been shown to take input from local motion detectors consistent with the classic correlation model developed by Hassenstein and Reichardt in the 1950s. We have tested the hypothesis that similar mechanisms underlie the response of dragonfly STMDs. We show that an anatomically characterized centrifugal STMD neuron (CSTMD1) gives responses that depend strongly on target contrast, a clear prediction of the correlation model. Target stimuli are more complex in spatiotemporal terms than the sinusoidal grating patterns used to study LPTCs, so we used a correlation-based computer model to predict response tuning to velocity and width of moving targets. We show that increasing target width in the direction of travel causes a shift in response tuning to higher velocities, consistent with our model. Finally, we show how the morphology of CSTMD1 allows for impressive spatial interactions when more than one target is present in the visual field.

energy expenditure to track flowers is minimal compared to energy intake; therefore, patterns of net energy gain mimicked patterns of feeding rate. The direction effects of flower motion were greater than the frequency effects. While M. sexta appeared equally capable of tracking flowers moving in the horizontal and vertical motion axes, they demonstrated poor ability to track flowers moving in the looming axis. Additionally, both feeding rates and net energy gain were lower for looming axis flower motions.

Declines in bumblebee populations have led to investigations into potential causes – including agrochemical effects on bumblebee physiology. The indirect effects of agrochemicals (i.e. behavior modulation) have been postulated, but rarely directly tested. Olfactory information is critical in mediating bumblebee-floral interactions. As agrochemicals emit volatiles, they may indirectly modify foraging behavior. We tested the effects of olfactory contamination of floral odor by agrochemical scent on foraging activity of Bombus impatiens using two behavioral paradigms: localization of food within a maze and forced-choice preference. The presence of a fungicide decreased bumblebees’ ability to locate food within a maze. Additionally, bumblebees preferred to forage in non-contaminated feeding chambers when offered a choice between control and either fertilizer- or fungicide-scented chambers.

While the phrase ‘foraging bumblebee’ brings to mind a bumbling bee flying flower to flower in a sunny meadow, foraging is a complicated series of behaviors such as: locating a floral patch; selecting a flower-type; learning handling skills for pollen and nectar extraction; determining when to move-on from a patch; learning within-patch paths (traplining); and learning efficient hive-to-patch routes (spatial navigation). Thus the term ‘forager’ encompasses multiple distinct behaviors that rely on different sensory modalities. Despite a robust literature on bumblebee foraging behavior, few studies are directly relevant to sensory-guided search; i.e. how workers locate novel patches. The first step in answering this question is to determine what sensory information is available to searching bumblebees. This manuscript presents a computational model that elucidates the relative frequency of visual and olfactory cues that are available to workers searching for floral resources under a range of ecologically relevant scenarios. Model results indicate that odor is the most common sensory cue encountered during search flights. When the likelihood of odor-plume contact is higher, odor-encounter is ubiquitous. While integrative (visual + olfactory) cues are common when foragers are searching for larger flowers (e.g. Echinacea), they become rare when foragers are searching for small flowers (e.g. Penstemon). Visual cues are only encountered in isolation when foragers are seeking large flowers with a low odor-plume contact probability. These results indicate that despite the multisensory nature of floral signals, different modalities may be encountered in isolation during search-behavior, as opposed to the reliably multimodal signals encountered during patch-exploitation or nectar/ pollen acquisition.

While plant-pollinator interactions are a classic model system for evolutionary relationships, the relationship between forager energetics and floral motions remains little explored. In this study, we show that hawkmoths preferentially feed on horizontally oscillating flowers, which have previously been shown to yield higher energy gains during feeding bouts than looming flowers. We also analyze natural flower motions exhibited by four hawkmoth-pollinated species. Our analysis shows these flowers have higher amplitude motions in the horizontal axis than that in the looming axis. This work demonstrates the potential for adaptation between the biomechanical determinates of flower motions and the feeding performance of hawkmoths.