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Haverkamp, A.

Publications and source records attributed to Haverkamp, A..

2 recordsLinked to original sources

Learning may help pollinators find their host plants in polluted landscapes

Pollination strongly contributes to food production, and often relies on pollinating insects. However, atmospheric pollution may interfere with pollination by disrupting floral plumes that pollinators use to navigate to flowers.\n\nIn this study, we examine the impacts of pollution-induced elevated ozone levels on the composition of a floral blend of Nicotiana alata and examine the response of innate and trained Manduca sexta to the ozone-altered blend.\n\nOzone exposure altered the floral blend of N. alata, and disrupted the innate attraction of naive M. sexta to the altered blend. However, associative learning can offset this disruption in attraction. Moths that were enticed with visual cues to an artificial flower emitting an ozonated blend learned to associate this blend with a nectar reward after just one rewarded experience. More importantly, moths that were rewarded while experiencing the unozonated floral blend of their host subsequently found the ozonated floral blend of the same host attractive, most likely due to experience-based reinforcement of ozone-insensitive cues in the blend.\n\nThe attraction of moths to both unaltered and ozonated plumes is critical for tolerating polluted landscapes. At the host plant, where moths feed, floral emissions are relatively pure. As floral odors travel away from the host, however, they become degraded by pollution. Therefore, targeting the flower requires recognizing both conditions of the odor. The ability to generalize between the pure and ozone-altered scents may enable pollinators like M. sexta to maintain communication with their flowers and reduce the impact anthropogenic oxidants may have on plant-pollinator systems.

animal behavior and cognition

Mutagenesis of orco impairs foraging but not oviposition in the hawkmoth Manduca sexta

Plant volatile detection through olfaction plays a crucial role in insect behaviors. In vivo, the odorant receptor co-receptor orco is an obligatory component for the function of odorant receptors (ORs), a major receptor family involved in insect olfaction. We used CRISPR-Cas9 targeted mutagenesis to knock-out (KO) orco in a neurophysiological model species, the hawkmoth Manduca sexta. M. sexta and its host, the Sacred Datura (Datura wrightii) share a model insect-plant relationship based on mutualistic and antagonistic life history traits. D. wrightii is the innately preferred nectar-source and oviposition host for M. sexta. Hence, the hawkmoth is an important pollinator while the M. sexta larvae are specialized herbivores of the plant. We generated an orco KO through CRISPR-Cas9 to test the consequences of a loss of OR-mediated olfaction in this insect-plant relationship. Neurophysiological characterization revealed severely reduced antennal and antennal lobe responses to representative odorants emitted by D. wrightii. In a wind-tunnel setting with a flowering plant, orco KO hawkmoths showed disrupted flight orientation and an ablated proboscis extension response to the natural stimulus. However, when testing the oviposition behavior of mated females encountering a non-flowering plant, there was no difference between orco KO and wild type females regarding upwind flight orientation and number of eggs laid. Overall, OR-mediated olfaction is essential for foraging and pollination behaviors, but plant-seeking and oviposition behaviors appear largely unaffected. Significance statementInsects detect plant volatiles mainly through the expression of ORs and IRs on the antennal olfactory sensory neurons (OSNs). In vivo, Orco is an obligate partner for OR, but not IR function and ORs mediate a vast spectrum of olfactory perception. We applied CRISPR-Cas9 in M. sexta to mutate the orco gene and determine the physiological and behavioral implication of a loss of Orco receptor function in a semi-ecological interaction with D. wrightii. We found that while behaviors related to foraging were largely disrupted, other sensory modalities outside Orco function determine the relationship between an ovipositing female and its plant host. These results have implications toward understanding the olfactory basis of insect-plant interactions shaping our ecological and agricultural landscapes.

neuroscience