In times of environmental change species have two options to survive: they either relocate to a new habitat or they adapt to the altered environment. Adaptation requires physiological plasticity and provides a selection benefit. In this regard, the Western honeybee (Apis mellifera) protrudes with its thermoregulatory capabilities, which enables a nearly worldwide distribution. Especially in the cold, shivering thermogenesis enables foraging as well as proper brood development and thus survival. In this study, we present octopamine signaling as a neurochemical prerequisite for honeybee thermogenesis: we were able to induce hypothermia by depleting octopamine in the flight muscles. Additionally, we could restore the ability to increase body temperature by administering octopamine. Thus, we conclude that octopamine signaling in the flight muscles is necessary for thermogenesis. Moreover, we show that these effects are mediated by β octopamine receptors. The significance of our results is highlighted by the fact the respective receptor genes underlie enormous selective pressure due to adaptation to cold climates. Finally, octopamine signaling in the service of thermogenesis might be a key strategy to survive in a changing environment.
In recent decades, our planet has undergone dramatic environmental changes resulting in the loss of numerous species. This contrasts with species that can adapt quickly to rapidly changing ambient conditions, which require physiological plasticity and must occur rapidly. The Western honeybee (Apis mellifera) apparently meets this challenge with remarkable success, as this species is adapted to numerous climates, resulting in an almost worldwide distribution. Here, coordinated individual thermoregulatory activities ensure survival at the colony level and thus the transmission of genetic material. Recently, we showed that shivering thermogenesis, which is critical for honeybee thermoregulation, depends on octopamine signaling. In this study, we tested the hypothesis that the thoracic neuro-muscular octopaminergic system strives for a steady-state equilibrium under cold stress to maintain endogenous thermogenesis. We can show that this applies for both, octopamine provision by flight muscle innervating neurons and octopamine receptor expression in the flight muscles. Additionally, we discovered alternative splicing for AmOARβ2. At least the expression of one isoform is needed to survive cold stress conditions. We assume that the thoracic neuro-muscular octopaminergic system is finely tuned in order to contribute decisively to survival in a changing environment.
In times of environmental change species have two options to survive: they either relocate to a new habitat or they adapt to the altered environment. Adaptation requires physiological plasticity and provides a selection benefit. In this regard, the Western honeybee (Apis mellifera) protrudes with its thermoregulatory capabilities, which enables a nearly worldwide distribution. Especially in the cold, shivering thermogenesis enables foraging as well as proper brood development and thus survival. In this study, we present octopamine signaling as a neurochemical prerequisite for honeybee thermogenesis: we were able to induce hypothermia by depleting octopamine in the flight muscles. Additionally, we could restore the ability to increase body temperature by administering octopamine. Thus we conclude, that octopamine is necessary and sufficient for thermogenesis. Moreover, we show that these effects are mediated by β octopamine receptors. The significance of our results is highlighted by the fact the respective receptor genes underlie enormous selective pressure due to adaptation to cold climates. Finally, octopamine signaling in the service of thermogenesis might be a key strategy to survive in a changing environment.
Thrips (Thysanoptera) have been recorded as pollinators of various plant species, but they are mostly regarded to be of low ecological relevance. In Southeast Asia, thrips were recently discovered to pollinate flowers of several taxonomic sections of the pioneer tree genus Macaranga (Euphorbiaceae), which is particularly well known as an ant-plant, and for its importance in early forest succession. The lack of taxonomic treatment and of knowledge about systematic relationships among extant thrips, however, has prevented firm conclusions on the specificity of this plant-pollinator interaction. Here, results from sequencing of the mitochondrial cytochrome oxidase subunit support our previous morphospecies concept of Macaranga flower thrips, and confirm the genetic identity of five recently described species. They were remarkably all assigned to the genus Dolichothrips (Phlaeothripidae), which typically consists of phytophagous species. In addition, the molecular data revealed one cryptic species. A first phylogenetic tree of the Dolichothrips associated with Macaranga provides insights into their systematic position. In particular, we identify monophyly of all important Macaranga pollinator species, all species being largely specific to particular taxonomic host plant sections. Our results suggest a closely matched diversification of pollinating thrips with Macaranga trees. This adds a novel type of association to thrips pollinator-plant interactions, which have been so far documented as single-species interactions or generalist thrips species visiting multiple plant taxa.
The behavioral state of an animal has profound effects on neuronal information processing. Locomotion changes the response properties of visual interneurons in the insect brain, but it is still unknown if it also alters the response properties of photoreceptors. Photoreceptor responses become faster at higher temperatures. It has therefore been suggested that thermoregulation in bees and other insects could improve temporal resolution in vision, but direct evidence for this idea has so far been missing. Here we compared electroretinograms (ERGs) from the compound eyes of tethered bumblebees that were either sitting still or were walking on an air supported ball. We found that the visual processing speed strongly increased when the bumblebees were walking. By monitoring the bumblebees′ eye temperature during our recordings, we saw that the increase in response speed was in synchrony with a rise of the eye temperature. By artificially heating the bee′s head, we show that the walking induced temperature increase of the visual system is sufficient to explain the rise in processing speed. We also show that walking accelerates the visual system to the equivalent of a 14-fold increase in light intensity. We conclude that the walking-induced rise in temperature accelerates the processing of visual information in bumblebees, which is an ideal strategy to process the increased information flow during locomotion.
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