Ecology and Vulnerability
Eastern Small-footed Bat

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Eastern Small-Footed Bat

Photo Credit: Paul Moosman

Scientific name
Myotis leibii

Profile: Eastern Small-footed Bat ▾▸

There was not much information about the biological responses to climate change of the Northeast’s bat RSGCN identified in the literature search. However, bats in the northeastern U.S. will likely be...

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There was not much information about the biological responses to climate change of the Northeast’s bat RSGCN identified in the literature search. However, bats in the northeastern U.S. will likely be especially sensitive to climate change because much of their biology, including reproduction and hibernation, is closely related to temperature (Loeb and Winters 2013). For instance, increasing winter temperatures will likely cause warmer microsites where bats hibernate (Boyles et al., 2017), and variation in ambient microsite temperature increases energy expenditure by hibernating bats (Boyles and McKechnie, 2010). Hibernacula near cave entrances are quickly affected by outside temperatures, as opposed to sites deeper in caves, which are more shielded (Boyles et al., 2017). However, even small temperature variations can significantly increase energy expenditure across winter (Boyles and McKechnie 2010), so areas with a large range of microclimates may hold on to their bat populations while those with a more limited range may not (Boyles et al., 2017). Despite that, some evidence suggests that ambient temperature may not be the most important factor in energy conservation during hibernation, as behavior, humidity, and initial fat mass were also important factors for Tricolored Bats (McGuire et al., 2021) and Tricolored Bats experimentally held in varying temperatures during hibernation showed no difference in metabolic rate when hibernation ended (Boyles et al., 2022). 


Variations in precipitation patterns that lead to increased drought and more extreme storms will likely affect foraging conditions for bats. Insect populations often decline during drought (Hawkins and Holyoak 1998), resulting in increased foraging costs and decreased annual survival for bats (Loeb and Winters 2013). Most insectivorous bats must drink to maintain water balance, and water needs increase considerably during pregnancy and lactation (Kurta et al., 1989, 1990; Adams and Hayes 2008). As such, severe droughts, especially when combined with unusually cold or hot temperatures, will likely lead to lower reproductive success rates (Bourne and Hamilton-Smith 2007; Adams 2010). 


Changes in precipitation patterns are already contributing to more severe wildfires across North America, specifically in boreal forests (Stephens et al., 2014). The increased risk that wildfires may impose on bat populations is not well known (Jung 2020); though, studies evaluating the effect of smaller, prescribed burns have shown burned areas benefit bats in creating better roosting and foraging opportunities (e.g., Ford et al., 2016, O’Keefe and Loeb 2017). While smaller prescribed burns may increase bat activity in some areas, larger wildfires can have negative impacts on some species (e.g., Snider et al., 2013, but see Buchalski et al., 2013). For example, after a “megafire” in the boreal forest of Yukon, Canada, despite creating more open areas for Little Brown Bats to forage, bat activity in the burned areas was much lower than in nearby unburned areas, with almost no activity occurring in burned upland areas (Jung 2020). Importantly, sites of “megafires” in eastern Canada in the summer of 2023 may provide a good opportunity to work with Canadian colleagues to explore post-fire habitat usage.


There is still much to learn about how these ecologically important species that provide valuable ecosystem services as consumers of nuisance insects (CITE) are and will be impacted by climate change. Much of the research on these bat species has focused on roosting and hibernating site selection and how these sites may influence energy budgets. However, since bats are highly mobile, one particularly large data gap exists in considering how these species will shift their geographic ranges, especially for one species with a projected range shift (Indiana Bats) indicating it could abandon most of its summer range in the midwestern U.S. for the northeastern U.S. in the next 50 years (Loeb and Winters 2013). Having reasonable estimates of where these species may be in the near- and long-term is crucial in developing management plans for the future. While none of the northeastern bats of greatest conservation need had much research on biological responses to climate change, we found no research at all for one-third of these species. Other major data gaps include a complete lack of published data on how climate change will affect population trends or changes in the physiology and morphology of RSGCN bats in the Northeast and how any indirect effects of climate change will impact them.

 

References

Adams, R. A., & Hayes, M. A. (2008). Water availability and successful lactation by bats as related to climate change in arid regions of western North America. Journal of Animal Ecology.

Adams 2010

Bourne, S., & Hamilton-Smith, E. (2007). Miniopterus schreibersii bassanii and climate change. Australasian Bat Society Newsletter, 28, 67–69.

Boyles, J. G., Boyles, E., Dunlap, R. K., Johnson, S. A., & Brack, V. (2017). Long-term microclimate measurements add further evidence that there is no “optimal” temperature for bat hibernation. Mammalian Biology, 86, 9–16.

Boyles, J. G., Johnson, E. M., Fuller, N. W., Silas, K. A., Hou, L., Frick, W. F., & McGuire, L. P. (2022). Behavioural microclimate selection and physiological responses to environmental conditions in a hibernating bat. Canadian Journal of Zoology, 100(3), 233–238.

Boyles, J. G., & McKechnie, A. E. (2010). Energy conservation in hibernating endotherms: Why “suboptimal” temperatures are optimal. Ecological Modelling, 221(12), 1644–1647.

Buchalski et al., 2013

Ford, W. M., Silvis, A., Johnson, J. B., Edwards, J. W., & Karp, M. (2016). Northern long-eared bat day-roosting and prescribed fire in the central Appalachians, USA. Fire Ecology, 12, 13–27.

Hawkins, B. A., & Holyoak, M. (1998). Transcontinental crashes of insect populations? The American Naturalist, 152(3), 480–484.

Jung, T. S. (2020). Bats in the changing boreal forest: Response to a megafire by endangered little brown bats (Myotis lucifugus). Ecoscience, 27(1), 59–70.

Kurta, A., Bell, G. P., Nagy, K. A., & Kunz, T. H. (1989). Energetics of pregnancy and lactation in free ranging little brown bats (Myotis lucifugus). Physiological Zoology, 62(3), 804– 818.

Kurta et al., 1990

Loeb, S. C., & Winters, E. A. (2013). Indiana bat summer maternity distribution: Effects of current and future climates. Ecology and Evolution, 3(1), 103–114.

McGuire, L. P., Johnson, E. M., Frick, W. F., & Boyles, J. G. (2021). Temperature alone is insufficient to understand hibernation energetics. Journal of Experimental Biology, 224(14), 239772.

O’Keefe, J. M., & Loeb, S. C. (2017). Indiana bats roost in ephemeral, fire-dependent pine snags in the southern Appalachian Mountains, USA. Forest Ecology and Management, 391, 264–274.

Snider, E. A., Cryan, P. M., & Wilson, K. R. (2013). Roost selection by western long-eared myotis (Myotis evotis) in burned and unburned piñon–juniper woodlands of southwestern Colorado. Journal of Mammalogy, 94(3), 640–649.

Stephens, S. L., Burrows, N., Buyantuyev, A., Gray, R. W., Keane, R. E., Kubian, R., & Wagtendonk, J. W. (2014). Temperate and boreal forest mega‐fires: Characteristics and challenges. Frontiers in Ecology and the Environment, 12(2), 115–122.