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Native predators provide undervalued pest suppression services to agriculture. Studies of pest consumption by insectivorous bats tend to focus upon single species in large, centralized colonies, while bats dispersed in small groups within the agricultural matrix often go unnoticed. Pecan trees, Carya illinoinensis, and the destructive pecan nut casebearer (PNC) moth, Acrobasis nuxvorella, comprise a tightly linked host&ndash, parasite system in a widespread agroecosystem native to North America. Here we use a quantitative polymerase chain reaction (qPCR) assay of fecal DNA to document predation on PNC moths by an assemblage of sympatric bat species across episodic peaks in PNC abundance. Although five species of bats consume PNC moths, greater predation by a solitary tree-roosting bat (eastern red bat, Lasiurus borealis) than other species is suggested by a higher frequency of PNC occurrence and quantity of PNC gene copies in fecal samples. Consumption of PNC by bats during all documented peaks in moth activity suggests that predation pressure occurs throughout the PNC season. Our results highlight the need to consider multi-species assemblages and different foraging strategies when assessing pest suppression services, particularly in agroforestry or tree crops. Assessing the diet of only common or easily captured species limits our ability to accurately document pest consumption by bats.

Landscape complexity influences patterns of animal dispersal, which in turn may affect both gene flow and the spread of pathogens. White-nose syndrome (WNS) is an introduced fungal disease that has spread rapidly throughout eastern North America, causing massive mortality in bat populations. We tested for a relationship between the population genetic structure of the most common host, the little brown myotis (Myotis lucifugus), and the geographic spread of WNS to date by evaluating logistic regression models of WNS risk among hibernating colonies in eastern North America. We hypothesized that risk of WNS to susceptible host colonies should increase with both geographic proximity and genetic similarity, reflecting historical connectivity, to infected colonies. Consistent with this hypothesis, inclusion of genetic distance between infected and susceptible colonies significantly improved models of disease spread, capturing heterogeneity in the spatial expansion of WNS despite low levels of genetic differentiation among eastern populations. Expanding our genetic analysis to the continental range of little brown myotis reveals strongly contrasting patterns of population structure between eastern and western North America. Genetic structure increases markedly moving westward into the northern Great Plains, beyond the current distribution of WNS. In western North America, genetic differentiation of geographically proximate populations often exceeds levels observed across the entire eastern region, suggesting infrequent and/or locally restricted dispersal, and thus relatively limited opportunities for pathogen introduction in western North America. Taken together, our analyses suggest a possibly slower future rate of spread of the WNS pathogen, at least as mediated by little brown myotis.

In response to seasonal variation in energy availability and thermal environment, physiological and endocrine mechanisms have evolved in temperate zone animals. Seasonal changes in hormone activity affect metabolism, body temperature, and reproductive activity. We examined the seasonal regulatory role of hormones on basal metabolic rate (BMR) and regulatory nonshivering thermogenesis (RNST) in 98 female and 17 male adult Eptesicus fuscus (big brown bat). We measured BMR, RNST, and plasma levels of thyroid hormone (T3), leptin, and cortisol in bats captured in maternity colonies in eastern Massachusetts from May to August (from arousal from the hibernation phase to the prehibernation phase). We hypothesized that all three hormones are seasonally primarily metabolic hormones and secondarily thermogenic hormones. In males, only BMR significantly changed seasonally. In females, all five variables significantly changed seasonally. The seasonal pattern of plasma leptin and cortisol levels correlated with the seasonal pattern of BMR, with an initial increase followed by a decrease, suggesting that leptin and cortisol are primarily metabolic hormones. The seasonal pattern of plasma T3 levels generally paralleled the basic seasonal pattern of RNST, with both increasing at the second half of the season, suggesting that T3 is primarily a thermogenic hormone. The observed decrease in plasma leptin levels may be necessary to allow for the observed seasonal decrease in BMR, with the similar cortisol pattern important for leptin regulation. While T3 is needed to maintain BMR, it may play a more critical role in the seasonal regulation of RNST than of BMR.

The insectivorous bat Myotis lucifugus typically apportions the night into two foraging periods separated by an interval of night roosting. During this interval, many bats occupy roosts that are used exclusively at night and are spatially separate from maternity roosts. The proportion of the night which bats spend roosting, and thus the proportion spent foraging, vary both daily and seasonally in relation to the reproductive condition of the bats, prey density, and ambient temperature. A single, continuous night roosting period is observed during pregnancy. During lactation, females return to maternity roosts between foraging bouts, and night roosts are used only briefly and sporadically. Maximum use of night roosts occurs in late summer after young become volant. Superimposed upon these seasonal trends is day-to-day variation in the bats' nightly time budget. Long night roosting periods and short foraging periods are associated with cool nights and low prey density. This behavioral response may minimize energetic losses during periods of food scarcity.

The performance capabilities of flying animals reflect the interplay of biomechanical and physiological constraints and evolutionary innovation. Of the two extant groups of vertebrates that are capable of powered flight, birds are thought to fly more efficiently and faster than bats. However, fast-flying bat species that are adapted for flight in open airspace are similar in wing shape and appear to be similar in flight dynamics to fast-flying birds that exploit the same aerial niche. Here, we investigate flight behaviour in seven free-flying Brazilian free-tailed bats (Tadarida brasiliensis) and report that the maximum ground speeds achieved exceed speeds previously documented for any bat. Regional wind modelling indicates that bats adjusted flight speeds in response to winds by flying more slowly as wind support increased and flying faster when confronted with crosswinds, as demonstrated for insects, birds and other bats. Increased frequency of pauses in wing beats at faster speeds suggests that flap-gliding assists the bats' rapid flight. Our results suggest that flight performance in bats has been underappreciated and that functional differences in the flight abilities of birds and bats require re-evaluation.

This article provides a brief overview and a few glimpses of how various factors influence the reproductive energetics of terrestrial reptiles, birds, and mammals. The amount of energy allocated to various phases of reproduction (courtship and mating, incubation, gestation, lactation, parental care, and the pre- and postfledging or postlactational periods) is, in part, influenced by the type of reproduction (oviparity vs. vivaparity), different types of mating system (monogamy, polygyny, and polyandry), rates of posthatching and postnatal growth, competitive interactions with members of the same or different species, and extrinsic factors such as habitat quality, food availability, and climate. In general, costs of courtship and mating are higher for males that typically compete for females by developing elaborate structures or behaviors used in courtship display to show females that they are fit and by defending either mating territories or females. The energy investment that male vertebrates make in the production of gametes is relatively small compared with that made by females, and female reptiles and birds typically invest more in egg production (both size and number) than do female mammals. Apart from the production of a relatively large number of eggs, few reptiles exhibit maternal care once the young hatch. In contrast, birds and mammals often invest extensively in their young once they hatch or are born. Female birds allocate large amounts of energy to brooding and feeding their young until they have reached or exceed adult size. Some bird species invest further in their offspring by tutoring them once they have fledged. In contrast, mammals typically produce a relatively small number of eggs that are fertilized internally, the fetus develops in the uterus that is protected from environmental extremes, young are born alive, and females nurse their young with milk for variable periods of time and in many species may provide extended care to their offspring. Among males, courtship and mating are the most energetically expensive activities in reptiles, birds, and mammals. The production of nutrient- and energy-rich eggs is the most energetically expensive phase of reproduction in female reptiles. Production and incubation of eggs and feeding of nestlings comprise the most energetically expensive phase of reproduction in female birds. Lactation is the most energetically expensive period of reproduction in female mammals. In addition to the physiological costs of reproduction, we describe how some mammals may expend energy to provide behavioral forms of parental care (including paternal and alloparental care); however field data quantifying these activities are severely lacking, so their costs are rarely included in studies on reproductive energetics.

Disease can play an important role in structuring species communities because the effects of disease vary among hosts; some species are driven towards extinction, while others suffer relatively little impact. Why disease impacts vary among host species remains poorly understood for most multi-host pathogens, and factors allowing less-susceptible species to persist could be useful in conserving highly affected species. White-nose syndrome (WNS), an emerging fungal disease of bats, has decimated some species while sympatric and closely related species have experienced little effect. We analysed data on infection prevalence, fungal loads and environmental factors to determine how variation in infection among sympatric host species influenced the severity of WNS population impacts. Intense transmission resulted in almost uniformly high prevalence in all species. By contrast, fungal loads varied over 3 orders of magnitude among species, and explained 98% of the variation among species in disease impacts. Fungal loads increased with hibernating roosting temperatures, with bats roosting at warmer temperatures having higher fungal loads and suffering greater WNS impacts. We also found evidence of a threshold fungal load, above which the probability of mortality may increase sharply, and this threshold was similar for multiple species. This study demonstrates how differences in behavioural traits among species—in this case microclimate preferences—that may have been previously adaptive can be deleterious after the introduction of a new pathogen. Management to reduce pathogen loads rather than exposure may be an effective way of reducing disease impact and preventing species extinctions. This article is part of the themed issue ‘Tackling emerging fungal threats to animal health, food security and ecosystem resilience’.

Seasonal patterns in pathogen transmission can influence the impact of disease on populations and the speed of spatial spread. Increases in host contact rates or births drive seasonal epidemics in some systems, but other factors may occasionally override these influences. White-nose syndrome, caused by the emerging fungal pathogen Pseudogymnoascus destructans , is spreading across North America and threatens several bat species with extinction. We examined patterns and drivers of seasonal transmission of P. destructans by measuring infection prevalence and pathogen loads in six bat species at 30 sites across the eastern United States. Bats became transiently infected in autumn, and transmission spiked in early winter when bats began hibernating. Nearly all bats in six species became infected by late winter when infection intensity peaked. In summer, despite high contact rates and a birth pulse, most bats cleared infections and prevalence dropped to zero. These data suggest the dominant driver of seasonal transmission dynamics was a change in host physiology, specifically hibernation. Our study is the first, to the best of our knowledge, to describe the seasonality of transmission in this emerging wildlife disease. The timing of infection and fungal growth resulted in maximal population impacts, but only moderate rates of spatial spread.