BAITING AND BANDING: EXPERT OPINION ON HOW BAIT TRAPPING MAY INFLUENCE THE OCCURRENCE OF HIGHLY PATHOGENIC AVIAN INFLUENZA (HPAI) AMONG DABBLING DUCKS.

A Eurasian lineage highly pathogenic avian influenza virus (HPAIV) of the clade 2.3.4.4b (Goose/Guangdong lineage) was detected in migratory bird populations in North America in December 2021, and it, along with its reassortants, have since caused wild and domestic bird outbreaks across the continent. Relative to previous outbreaks, HPAIV cases among wild birds in 2022 exhibited wider geographic extent within North America and higher levels of mortality, suggesting the potential for population-level impacts. Given the possible conservation implications of HPAIV in wild birds, natural resource managers have sought guidance on actions that may mitigate negative effects of disease among North American bird populations, including modification of existing management practices. Banding of waterfowl is a critical tool for population management for several harvested species in North America, but some banding techniques, such as bait trapping, can lead to increased congregation of waterfowl, potentially altering HPAIV transmission. We used an expert opinion exercise to assess how bait trapping of dabbling ducks in Canada may influence HPAIV transmission and wild bird health. The expert group found that it is moderately likely that bait trapping of dabbling ducks in wetlands will significantly increase the transmission of HPAIV among individual ducks, but there is a low probability that this will result in significant population-level effects on North American dabbling ducks. Considering the lack of empirical work studying how capture and handling methods may change transmission of HPAIV among waterfowl, as well as the importance of bait trapping for waterfowl management in North America, future work should focus on filling knowledge gaps pertaining to the influence of baiting on HPAIV occurrence to better inform banding procedures and management decision making.

Captive-reared migratory monarch butterflies show natural orientation when released in the wild.

Eastern North American migratory monarch butterflies (Danaus plexippus) have faced sharp declines over the past two decades. Captive rearing of monarch butterflies is a popular and widely used approach for both public education and conservation. However, recent evidence suggests that captive-reared monarchs may lose their capacity to orient southward during fall migration to their Mexican overwintering sites, raising questions about the value and ethics of this activity undertaken by tens of thousands of North American citizens, educators, volunteers and conservationists each year. We raised offspring of wild-caught monarchs on swamp milkweed (Asclepias incarnata) indoors at 29°C during the day and 23°C at night (~77% RH, 18L:6D), and after eclosion, individuals were either tested in a flight simulator or radio tracked in the wild using an array of automated telemetry towers. While 26% (10/39) of monarchs tested in the flight simulator showed a weakly concentrated southward orientation, 97% (28/29) of the radio-tracked individuals that could be reliably detected by automated towers flew in a south to southeast direction from the release site and were detected at distances of up to 200 km away. Our results suggest that, although captive rearing of monarch butterflies may cause temporary disorientation, proper orientation is likely established after exposure to natural skylight cues.

Effects of early-life exposure to sublethal levels of a common neonicotinoid insecticide on the orientation and migration of monarch butterflies (Danaus plexippus).

Migratory insects use a variety of innate mechanisms to determine their orientation and maintain correct bearing. For long-distance migrants, such as the monarch butterfly (Danaus plexippus), these journeys could be affected by exposure to environmental contaminants. Neonicotinoids are synthetic insecticides that work by affecting the nervous system of insects, resulting in impairment of their mobility, cognitive performance, and other physiological and behavioural functions. To examine how neonicotinoids might affect the ability of monarch butterflies to maintain a proper directional orientation on their ∼4000 km migration, we grew swamp milkweed (Asclepias incarnata) in soil that was either untreated (0 ng g-1: control) or mixed with low (15 ng g-1 of soil) or high (25 ng g-1 of soil) levels of the neonicotinoid clothianidin. Monarch caterpillars were raised on control or clothianidin-treated milkweed and, after pupation, either tested for orientation in a static flight simulator or radio-tracked in the wild during the autumn migration period. Despite clothianidin being detectable in milkweed tissue consumed by caterpillars, there was no evidence that clothianidin influenced the orientation, vector strength (i.e. concentration of direction data around the mean) or rate of travel of adult butterflies, nor was there evidence that morphological traits (i.e. mass and forewing length), testing time, wind speed or temperature impacted directionality. Although sample sizes for both flight simulator and radio-tracking tests were limited, our preliminary results suggest that clothianidin exposure during early caterpillar development does not affect the directed flight of adult migratory monarch butterflies or influence their orientation at the beginning of migration.

Environmentally persistent pathogens present unique challenges for studies of host-pathogen interactions: Reply to Field (2018).

Linked article: https://doi.org/10.1002/ece3.4034.

The other white-nose syndrome transcriptome: Tolerant and susceptible hosts respond differently to the pathogen Pseudogymnoascus destructans.

Mitigation of emerging infectious diseases that threaten global biodiversity requires an understanding of critical host and pathogen responses to infection. For multihost pathogens where pathogen virulence or host susceptibility is variable, host-pathogen interactions in tolerant species may identify potential avenues for adaptive evolution in recently exposed, susceptible hosts. For example, the fungus Pseudogymnoascus destructans causes white-nose syndrome (WNS) in hibernating bats and is responsible for catastrophic declines in some species in North America, where it was recently introduced. Bats in Europe and Asia, where the pathogen is endemic, are only mildly affected. Different environmental conditions among Nearctic and Palearctic hibernacula have been proposed as an explanation for variable disease outcomes, but this hypothesis has not been experimentally tested. We report the first controlled, experimental investigation of response to P. destructans in a tolerant, European species of bat (the greater mouse-eared bat, Myotis myotis). We compared body condition, disease outcomes and gene expression in control (sham-exposed) and exposed M. myotis that hibernated under controlled environmental conditions following treatment. Tolerant M. myotis experienced extremely limited fungal growth and did not exhibit symptoms of WNS. However, we detected no differential expression of genes associated with immune response in exposed bats, indicating that immune response does not drive tolerance of P. destructans in late hibernation. Variable responses to P. destructans among bat species cannot be attributed solely to environmental or ecological factors. Instead, our results implicate coevolution with the pathogen, and highlight the dynamic nature of the "white-nose syndrome transcriptome." Interspecific variation in response to exposure by the host (and possibly pathogen) emphasizes the importance of context in studies of the bat-WNS system, and robust characterization of genetic responses to exposure in various hosts and the pathogen should precede any attempts to use particular bat species as generalizable "model hosts."

Energetic benefits of enhanced summer roosting habitat for little brown bats (Myotis lucifugus) recovering from white-nose syndrome.

Habitat modification can improve outcomes for imperilled wildlife. Insectivorous bats in North America face a range of conservation threats, including habitat loss and white-nose syndrome (WNS). Even healthy bats face energetic constraints during spring, but enhancement of roosting habitat could reduce energetic costs, increase survival and enhance recovery from WNS. We tested the potential of artificial heating of bat roosts as a management tool for threatened bat populations. We predicted that: (i) after hibernation, captive bats would be more likely to select a roost maintained at a temperature near their thermoneutral zone; (ii) bats recovering from WNS at the end of hibernation would show a stronger preference for heated roosts compared with healthy bats; and (iii) heated roosts would result in biologically significant energy savings. We housed two groups of bats (WNS-positive and control) in separate flight cages following hibernation. Over 7.5 weeks, we quantified the presence of individuals in heated vs. unheated bat houses within each cage. We then used a series of bioenergetic models to quantify thermoregulatory costs in each type of roost under a number of scenarios. Bats preferentially selected heated bat houses, but WNS-affected bats were much more likely to use the heated bat house compared with control animals. Our model predicted energy savings of up to 81.2% for bats in artificially heated roosts if roost temperature was allowed to cool at night to facilitate short bouts of torpor. Our results are consistent with research highlighting the importance of roost microclimate and suggest that protection and enhancement of high-quality, natural roosting environments should be a priority response to a range of threats, including WNS. Our findings also suggest the potential of artificially heated bat houses to help populations recover from WNS, but more work is needed before these might be implemented on a large scale.

Conspecific disturbance contributes to altered hibernation patterns in bats with white-nose syndrome.

The emerging wildlife disease white-nose syndrome (WNS) affects both physiology and behaviour of hibernating bats. Infection with the fungal pathogen Pseudogymnoascus destructans (Pd), the first pathogen known to target torpid animals, causes an increase in arousal frequency during hibernation, and therefore premature depletion of energy stores. Infected bats also show a dramatic decrease in clustering behaviour over the winter. To investigate the interaction between disease progression and torpor expression we quantified physiological (i.e., timing of arousal, rewarming rate) and behavioural (i.e., arousal synchronisation, clustering) aspects of rewarming events over four months in little brown bats (Myotis lucifugus) experimentally inoculated with Pd. We tested two competing hypotheses: 1) Bats adjust arousal physiology adaptively to help compensate for an increase in energetically expensive arousals. This hypothesis predicts that infected bats should increase synchronisation of arousals with colony mates to benefit from social thermoregulation and/or that solitary bats will exhibit faster rewarming rates than clustered individuals because rewarming costs fall as rewarming rate increases. 2) As for the increase in arousal frequency, changes in arousal physiology and clustering behaviour are maladaptive consequences of infection. This hypothesis predicts no effect of infection or clustering behaviour on rewarming rate and that disturbance by normothermic bats contributes to the overall increase in arousal frequency. We found that arousals of infected bats became more synchronised than those of controls as hibernation progressed but the pattern was not consistent with social thermoregulation. When a bat rewarmed from torpor, it was often followed in sequence by up to seven other bats in an arousal "cascade". Moreover, rewarming rate did not differ between infected and uninfected bats, was not affected by clustering and did not change over time. Our results support our second hypothesis and suggest that disturbance, not social thermoregulation, explains the increased synchronisation of arousals. Negative pathophysiological effects of WNS on energy conservation may therefore be compounded by maladaptive changes in behaviour of the bats, accelerating fat depletion and starvation.

Hormones and hibernation: possible links between hormone systems, winter energy balance and white-nose syndrome in bats.

This article is part of a Special Issue "Energy Balance". Hibernation allows mammals to survive in cold climates and during times of reduced food availability. Drastic physiological changes are required to maintain the energy savings that characterize hibernation. These changes presumably enable adjustments in endocrine activity that control metabolism and body temperature, and ultimately influence expression of torpor and periodic arousals. Despite challenges that exist when examining hormonal pathways in small-bodied hibernators, bats represent a potential model taxon for comparative neuroendocrinological studies of hibernation due to their diversity of species and the reliance of many species on heterothermy. Understanding physiological mechanisms underlying hibernation in bats is also important from a conservation physiology perspective due to white-nose syndrome, an emerging infectious disease causing catastrophic mortality among hibernating bats in eastern North America. Here we review the potential influence of three key hormonal mechanisms--leptin, melatonin and glucocorticoids--on hibernation in mammals with an emphasis on bats. We propose testable hypotheses about potential effects of WNS on these systems and their evolution.