Tri-colored Bat

Perimyotis subflavus (Menu, 1984)

Tri-colored bat (Perimyotis subflavus)
Al Hicks, NYSDEC

Mammalia (Mammals)
Vespertilionidae (Evening Bats and Vesper Bats)
State Protection
Not Listed
Not listed or protected by New York State.
Federal Protection
Proposed Endangered
Proposed for Listing as Endangered under the Federal Endangered Species Act
State Conservation Status Rank
Critically Imperiled in New York - Especially vulnerable to disappearing from New York due to extreme rarity or other factors; typically 5 or fewer populations or locations in New York, very few individuals, very restricted range, very few remaining acres (or miles of stream), and/or very steep declines.
Global Conservation Status Rank
Vulnerable globally, or Apparently Secure - At moderate risk of extinction, with relatively few populations or locations in the world, few individuals, and/or restricted range; or uncommon but not rare globally; may be rare in some parts of its range; possibly some cause for long-term concern due to declines or other factors. More information is needed to assign either G3 or G4.


Did you know?

The tri-colored bat (Perimyotis subflavus) was formerly known as the eastern pipistrelle (Pipistrellus subflavus). It was first recommended for placement in a separate genus in 2003 (Hoofer and Van Den Bussche 2003).

State Ranking Justification

Tri-colored bats were likely never common in New York. Although their northern range extends into Canada, New York is peripheral to the core of their range. The statewide population numbers have declined dramatically since the effects of WNS were first observed in 2006.

Short-term Trends

Tri-colored bat populations have declined approximately 96% in New York State from 2007 through 2015. There were only 118 tri-colored bats counted in 2012 compared with 2,285 among the same 37 hibernacula surveyed in 2007 (NYSDEC 2012).

Long-term Trends

Tri-colored bat numbers are presumed to have been stable or increasing prior to the start of WNS in 2006 (C. Herzog pers. comm.). 

Conservation and Management

Conservation Overview

Tri-colored bats use open woodlands and riparian forests. Populations in New York and the eastern U.S. have plummeted since White-nose Syndrome (WNS) was first reported in 2006.


By far the largest threat to tri-colored bats in New York is white-nose syndrome (WNS) which was first discovered among bats in a cave in Schoharie County, New York in 2006. White-nose syndrome is caused by a fungus Pseudogymnoascus destructans (previously Geomyces destructans) that is often visible on the bats muzzle and wings (Blehert et al. 2009). The fungus may invade hair follicles and cause lesions under the skin (Blehert et al. 2009). Bats wake from hibernation and consequently burn fat reserves that are needed to survive the winter and they become emaciated (Blehert et al. 2009). Extensive damage to their wing membranes and dehydration may also be contributing factors to mortality (U.S. Fish and Wildlife Service 2013).
Bats may be particularly sensitive to environmental toxins including those found in herbicides and pesticides. Although no studies have targeted tri-colored bats directly, elevated levels of persistent organic pollutants including PCBs, DDT, Chlordanes, and PBDEs have been found in a similar species, the little brown bat, in the Hudson River Valley in New York (Kannan et al. 2010). The levels found in the bats were only one to three times less than lethal concentrations reported from previous studies (Kannan et al. 2010). High toxin levels are expected in bats that obtain a high a composition of their diet from prey with an aquatic life stage. This may be a concern for tri-colored bats, as well, since caddisflies have been reported as an important food item in some regions (Carter et al. 2003; Feldhamer et al. 2009). Bats are highly susceptible to DDT residue, a chemical that was widely used as a pesticide to control bat infestations in houses in the 1940s (USGS 2013). DDT was widely used as an agricultural pesticide in the 1950s and 60s until its agricultural use was banned in 1972. Since DDT is highly persistent (soil half-life is 2-15 years, aquatic half-life is about 150 years) (NPIC 1999), it can pose a threat to bats when there is exposure to trace residues remaining in the environment (USGS 2013). Tri-colored bat populations were thought to have been impacted by heavy pesticide use in the mid-1950s (MA Natural Heritage Program 2012). Extensive applications of insecticides and some bio control methods, such as Btk could also pose an indirect risk to tri-colored bats by reducing availability of prey.
If proper precautions are not used, cavers and researchers entering hibernacula may cause disturbance that rouses bat colonies or can transport the fungus that causes WNS on their clothing (NatureServe 2013). Other potential threats may include climate change, commercial cave development, flooding and hibernacula collapse; habitat loss and fragmentation from development, hydraulic fracturing, and the construction of new wind facilities; and direct mortality from wind facilities (U.S. Fish and Wildlife Service 2013).

Conservation Strategies and Management Practices

Gating mines and caves can prevent human entry while allowing the bats unobstructed access. Following proper specifications and monitoring bat populations before and after gate installation are important, however, as gating can affect the airflow and temperature in the cave, making areas of the cave uninhabitable for certain species (U.S. Fish and Wildlife Service 2013). Buildup of debris at cave entrance gates can also have the same effect (U.S. Fish and Wildlife Service 2013).

Development and Mitigation Considerations

Retaining snags and dying trees can provide summer roosting habitat for tri-colored bats. Maintaining forested habitat in riparian corridors may also be important.

Research Needs

Research is needed to document summer roost locations and habitat in New York and to determine the extent of local populations. Research is also needed to identify regional differences in the characteristics of quality habitat and to identify areas of the state with the highest local abundances during summer. Ongoing winter hibernacula surveys are needed to monitor trends of the remaining populations.

Regional Conservation Needs

Conservation needs have not been determined for this species in New York. The extent of the current distribution of tri-colored bats in the state, as well as habitat requirements need to be determined prior to assessing specific management and conservation needs.



Tri-colored bats over-winter in humid areas deep within caves and mines with a constant temperature of around 52-55F (Griffin 1936; Godin 1977). A study in Arkansas found tri-colored bats selected larger caves with a wide range of temperatures within a season, but little variability among temperature between seasons (Briggler and Prather 2003). Surveys of hibernacula in New York conducted by the New York State Department of Environmental Conservation found tri-colored bats segregated from other species in warmer areas of the cave with high humidity.

Wooded riparian areas are likely an important foraging habitat for this species during the summer. One study in coastal South Carolina, found that tri-colored bats were more frequently found in riparian areas than in upland sites and especially, riparian areas that were wooded or highly vegetated (Menzel et al. 2005). They may also forage in woods or along waterways or forest edges (Fujita and Kunz 1984). Although tri-colored bats are typically considered a clutter-adapted species capable of foraging within forested areas, they also forage over early successional and open habitats (Loeb and O'Keefe 2006).

Tri-colored bats may roost in habitats including open woods near water and they may select roosts in buildings, crevices of cliffs and rocks, or in or below the canopy of live or recently dead trees that retain some dead or live leaves (Veilleux et al. 2003; Carter and Menzel 2006; Perry and Thill 2007). They are occasionally reported from caves during the summer (Godin 1977), and have been known to form maternity colonies in barns (Fujita and Kunz 1984), in clusters of dead leaves in oaks or pines (Perry and Thill 2007), and in Nova Scotia in lichen (Poissant et al. 2010). Perry et al. (2008) found that tri-colored bats tended to select roosts that were away from roads, in unharvested woods with high habitat heterogeneity, or in the unharvested riparian buffer of a partially harvested stand. Some habitat characteristics may vary regionally. Perry and Thill (2007) found tri-colored bats in mature forest stands with a hardwood component and a complex vertical structure and dense midstory. However, Yates and Muzika (2006) found that tri-colored bats favored open habitats with less dense mid-story vegetation and a dense understory.

Associated Ecological Communities

  • Allegheny oak forest (guide)
    A hardwood forest that occurs on well-drained sites in the unglaciated portion of southwestern New York. This is a forest of mixed oaks with a diverse canopy and richer ground flora than other oak communities in the state.
  • Appalachian oak-hickory forest (guide)
    A hardwood forest that occurs on well-drained sites, usually on ridgetops, upper slopes, or south- and west-facing slopes. The soils are usually loams or sandy loams. This is a broadly defined forest community with several regional and edaphic variants. The dominant trees include red oak, white oak, and/or black oak. Mixed with the oaks, usually at lower densities, are pignut, shagbark, and/or sweet pignut hickory.
  • Appalachian oak-pine forest (guide)
    A mixed forest that occurs on sandy soils, sandy ravines in pine barrens, or on slopes with rocky soils that are well-drained. The canopy is dominated by a mixture of oaks and pines.
  • Beech-maple mesic forest (guide)
    A hardwood forest with sugar maple and American beech codominant. This is a broadly defined community type with several variants. These forests occur on moist, well-drained, usually acid soils. Common associates are yellow birch, white ash, hop hornbeam, and red maple.
  • Maple-basswood rich mesic forest (guide)
    A species rich hardwood forest that typically occurs on well-drained, moist soils of circumneutral pH. Rich herbs are predominant in the ground layer and are usually correlated with calcareous bedrock, although bedrock does not have to be exposed. The dominant trees are sugar maple, basswood, and white ash.
  • Mine/artificial cave community
    The biota of an abandoned mine or artificial underground excavation. Abandoned mines that are deep enough to maintain stable winter temperatures are important bat hibernacula. Mines, like natural caves, may be terrestrial or aquatic. Wells are also included here.
  • Oak-tulip tree forest (guide)
    A hardwood forest that occurs on moist, well-drained sites in southeastern New York. The dominant trees include a mixture of five or more of the following: red oak, tulip tree, American beech, black birch, red maple, scarlet oak, black oak, and white oak.
  • Rich mesophytic forest (guide)
    A hardwood or mixed forest that resembles the mixed mesophytic forests of the Allegheny Plateau south of New York but is less diverse. It occurs on rich, fine-textured, well-drained soils that are favorable for the dominance of a wide variety of tree species. A canopy with a relatively large number of codominant trees characterizes this forest. Canopy codominants include five or more of the following species: red oak, red maple, white ash, American beech, sugar maple, black cherry, cucumber tree, and black birch.
  • Terrestrial cave community
    The terrestrial community of a cave with bedrock walls, including the biota of both solution caves (in limestone) and tectonic caves. Temperatures are stable in deep caves. Small or shallow caves may have a temperature gradient ranging from cold (below freezing) to cool (up to 50 degrees F). Although many caves have ice on the cave floor in winter, the ceiling is warm enough for a bat hibernaculum.

Associated Species

  • Big Brown Bat (Eptesicus fuscus)
  • Eastern Small-footed Myotis (Myotis leibii) (guide)
  • Little Brown Bat (Myotis lucifugus) (guide)
  • Northern Long-eared Bat (Myotis septentrionalis) (guide)
  • Indiana Bat (Myotis sodalis) (guide)


New York State Distribution

Prior to the start of WNS tri-colored bats were recorded in winter hibernacula in all regions of the state where mines and caves have been surveyed. They were more common (>10 individuals) in hibernacula in southern and western New York. The remaining distribution of tri-colored bats in New York is not known. Their statewide range may have contracted since the start of WNS.

Global Distribution

Tri-colored bats are found in eastern North America along the east coast as far south as Georgia and north into Nova Scotia and southern Quebec and Ontario. Their western range extent includes eastern Minnesota in the north and Texas to the northeast corner of Mexico in the south.

Identification Comments

General Description

The tri-colored bat is a medium-sized bat with tri-colored pelage on its back that ranges from dark grey at the base, to yellowish in the middle, and brown at the tip. They weigh 3.5-8 g (0.1-0.3 oz) and have a wingspan of 21-26 cm (8-10 in).

Identifying Characteristics

Tri-colored bats are best identified by their uniquely tri-colored, yellowish fur which is dark at the base and tip and light in the middle. Tri-colored bats may also be identified by their weak flight which is described as moth-like.

Best Life Stage for Proper Identification

Adults may be easiest to identify.


Tri-colored bats are nocturnal with periods of heightened activity at pre-dawn and dusk. They may range 5 miles from a roost to forage (MA Natural Heritage Program 2012).

Tri-colored bats are short-distance migrants traveling between winter hibernacula and summer habitat. The farthest known record was 52.8 km (Griffin 1940), although migration distances from hibernacula have not been extensively researched. Tri-colored bats may enter the hibernacula earlier in the fall and leave later in the spring compared to other species (Fujita and Kunz 1984).

Tri-colored bats breed in the fall and may breed again in the spring, coinciding with ovulation (Fujita and Kunz 1984). They swarm and mate near the cave entrance. Females store sperm over the winter until ovulation occurs in the spring, which coincides with emergence from winter hibernacula. Females generally give birth to two young.

Tri-colored bats often obtain insect prey by catching them in their tail and wing membranes. They may forage at varying heights, including within the canopy or above or below it (Menzel et al. 2005). They may forage in habitats such as woods, along waterways, or forest edges (Fujita and Kunz 1984).

Tri-colored bats are usually solitary but may be found roosting in small colonies; especially females which form maternity colonies in summer.


Tri-colored bats consume a diverse diet with several studies reporting that Diptera (flies) (Ross 1967; Whitaker 1972; Carter et al. 2003) and other soft-bodied prey (Carter et al. 2003) are an important component. One study in Indiana, found that tri-colored bats consumed primarily homopterans (cicadellids) and beetles with a smaller component of lepidopterans (Whitaker 2004). A study in Illinois found more than half their diet consisted of Trichopterans (caddisflies) followed by beetles and ants (Feldhamer et al. 2009). In West Virginia tri-colored bats consumed a wide mix of prey including Diptera, Hymenoptera, Tricoptera, Lepidoptera, and Homoptera (Carter et al. 2003). There are no known studies of the diet of this species from New York.

Best Time to See

Tri-colored bats may best be seen shortly after sunset or in the early morning before dawn in the late spring and summer. They are one of the first bats to emerge to forage in the evenings (Hamilton 1943). They have a slow, erratic flight pattern that may be distinguished from other species by an experienced observer.

  • Present
  • Active
  • Reproducing

The time of year you would expect to find Tri-colored Bat present, active, and reproducing in New York.

Tri-colored Bat Images


Tri-colored Bat
Perimyotis subflavus (Menu, 1984)

  • Kingdom Animalia
    • Phylum Craniata
      • Class Mammalia (Mammals)
        • Order Chiroptera (Bats)
          • Family Vespertilionidae (Evening Bats and Vesper Bats)

Additional Common Names

  • Eastern Pipistrelle


  • Pipistrellus subflavus (F. Cuvier, 1832)

Additional Resources


Blehert, D. S., A. C. Hicks, M. Behr, C. U. Meteyer, B. M. Berlowski-Zier, E. L. Buckles, et al. 2009. Bat white-nose syndrome: an emerging fungal pathogen? Science 323:227.

Briggler, J. T. and J. W. Prather. 2003. Seasonal use and selection of caves by the eastern pipistrelle bat (Pipistrellus subflavus). The American midland naturalist 149:406-12.

Carter, T. C. and J. M. Menzel. 2006. Day-roosting ecology and behavior of North American foliage-roosting bats. in M.J. Lacki, J.P. Hayes, and Kurta, eds. Conservation and management of forest bats. Johns Hopkins University Press, Baltimore, MD, USA.

Feldhamer, G. A., T. C. Carter and J. O. Whitaker. 2009. Prey Consumed by Eight Species of Insectivorous Bats from Southern Illinois. The American Midland Naturalist 162:43-51.

Fujita, M. S. and T. H. Kunz. 1984. Pipistrellus subflavus. Mammalian Species:1-6.

Godin, A. J. [online]. 1977. Wild mammals of New England. Johns Hopkins University Press Baltimore, MD.

Griffin, D. R. 1936. Bat banding. Journal of Mammalogy 17:235-239.

Griffin, D. R. 1940. Migrations of New England bats. The Museum.

Hamilton, W. J. [online]. 1943. mammals of eastern United States.

Hoofer, S. R. and R. A. Van Den Bussche. 2003. Molecular phylogenetics of the chiropteran family Vespertilionidae. Acta Chiropterologica 5:1-63.

Kannan, K., S. H. Yun, R. J. Rudd and M. Behr. 2010. High concentrations of persistent organic pollutants including PCBs, DDT, PBDEs and PFOS in little brown bats with white-nose syndrome in New York, USA. Chemosphere 80:613-618.

MA Natural Heritage Program [online]. 2012. Tricolored Bat. MA Natural Heritage Endangered Species Program Species and Conservation Guides. <> (11 February 2014).

Menzel, J. M., M. A. Menzel, J. C. Kilgo, W. M. Ford, J. W. Edwards and G. F. McCracken. 2005. Effect of habitat and foraging height on bat activity in the coastal plain of South Carolina. Journal of Wildlife Management 69:235-245.

NPIC [online]. 1999. National Pesticide Information Center DDT general fact sheet. <> (19 December 2013).

NYSDEC [online]. 2012. DEC Reports: 2012 Winter Bat Survey Results. Department of Environmental Conservation. <> (3 February 2014).

NatureServe [online]. 2013. NatureServe Explorer: an online encyclopedia of life [web application] Version 7.1. .

New York Natural Heritage Program. 2024. New York Natural Heritage Program Databases. Albany, NY.

Perry, R. W. and R. E. Thill. 2007. Tree roosting by male and female eastern pipistrelles in a forested landscape. Journal of Mammalogy 88:974-981.

Perry, R. W., R. E. Thill and D. M. Leslie. 2008. Scale-Dependent Effects of Landscape Structure and Composition on Diurnal Roost Selection by Forest Bats. The Journal of Wildlife Management 72:913-925.

Poissant, J. A., H. G. Broders and G. M. Quinn. 2010. Use of lichen as a roosting substrate by Perimyotis subflavus, the tricolored bat, in Nova Scotia. Ecoscience 17:372-378.

Ross, A. 1967. Ecological aspects of the food habits of insectivorous bats. Western Foundation of Vertebrate Zoology LA.

U.S. Fish and Wildlife Service. 2013. 12-Month finding on a petition to list the eastern small-footed bat and the northern long-eared bat as threatened or endangered; Listing the northern long-eared bat as an endangered species; Proposed rule. Vol. 78 No. 191, Department of the Interior.

USGS [online]. 2013. House Bat Management: Bat Toxicants. <> (19 December 2013).

Veilleux, J. P., J. O. Whitaker Jr and S. L. Veilleux. 2003. Tree-roosting ecology of reproductive female eastern pipistrelles, Pipistrellus subflavus, in Indiana. Journal of Mammalogy 84:1068-1075.

Whitaker, J. O. 1972. Food habits of bats from Indiana. Canadian Journal of Zoology 50:877-883.

Whitaker, J. O. 2004. Prey selection in a temperate zone insectivorous bat community. Journal of Mammalogy 85:460-469.

Yates, M. and R. Muzika. 2006. Effect of forest structure and fragmentation on site occupancy of bat species in Missouri Ozark forests. Journal of Wildlife Management 70:1238-1248.

About This Guide

This guide was authored by: Kelly A. Perkins

Information for this guide was last updated on: March 25, 2014

Please cite this page as:
New York Natural Heritage Program. 2024. Online Conservation Guide for Perimyotis subflavus. Available from: Accessed February 26, 2024.