E-Fauna BC: Electronic Atlas of the Wildlife of British Columbia

Myotis lucifugus (Le Conte)
Little Brown Bat; Little Brown Myotis
Family: Vespertilionidae
Species account authors: David Nagorsen and Mark Brigham.
Extracted from the Bats of British Columbia
Photo of species

© Paul Pratt  Email the photographer   (Photo ID #1614)

E-Fauna BC Static Map
Distribution of Myotis lucifugus in British Columbia
Details about map content are available here.


The information provided below is extracted from the Bats of British Columbia, and may be dated. Check the status section below for current status information.

Species Information

Click on the image(s) below to view an expanded illustration for this taxon.

Illustration Source: Bats of British Columbia by David Nagorsen and Mark Brigham © Royal BC Museum

The Little Brown Myotis is a medium-size species of Myotis. Its fur colour is extremely variable: the fur on its back ranges from yellow or olive in populations from the dry interior to blackish in coastal populations. The fur on its underside is lighter, varying from light brown to tan. Its dorsal fur is long and glossy. The wing membranes and ears are dark brown. The ears reach the nostrils when pushed forward; the tragus is blunt and about half the ear length. The calcar is not keeled. The skull is typical of most Myotis species; the forehead has a gradual slope.


The ear and tragus of the Little Brown Myotis are smaller than that of the Fringed Myotis (Myotis thysanodes), Northern Long-eared Myotis (Myotis septentrionalis), Western Long-eared Myotis (Myotis evotis) and Keen's Long-eared Myotis (Myotis keenii). The absence of a keel on the calcar distinguishes it from the Long-legged Myotis (Myotis volans), California Myotis (Myotis californicus) and Western Small-footed Myotis (Myotis ciliolabrum). The Yuma Myotis (Myotis yumanensis) is smaller (forearm usually less than 36 mm) with duller, shorter fur. Nevertheless, in some parts of the province, such as the Okanagan Valley, the Little Brown Myotis can be extremely difficult to distinguish from the Yuma Myotis. Behaviour may assist in identification. The Little Brown Myotis tends to be more aggressive than the Yuma Myotis when handled. Skull features will give a more reliable identification: Little Brown Myotis has a longer skull (greater than 14 mm) that has a more gradually sloping forehead; but even these characteristics are not always reliable in identifying some individuals with intermediate skull features.

Dental Formula

incisors: 2/3
canines: 1/1
premolars: 3/3
molars: 3/3


total length: 86 (70-108) n = 383
tail vertebrae: 37 (25-59) n = 379
hind foot: 10 (6-13) n = 385
ear: 13 (9-17) n = 217
tragus: 7 (4-10) n = 151
forearm: 36.4 (33.0-40.3) n = 295
wingspan: 248 (224-274) n = 151
weight: 6.2 (6.2-10.2) n = 98



Mating occurs in late summer and early autumn before entering hibernation. Males do not breed in their first autumn. Although yearling females can breed in their first year, in British Columbia most delay reproduction until their second autumn. After a gestation period of 50 to 60 days, a single young is born; twins are extremely rare. Birth dates vary, determined in part by the date when females arouse from hibernation. In the southern Okanagan Valley, females give birth between the second week of June and the second week of July. Populations living at higher elevations and latitudes probably have their young later. There are no data on birth dates for coastal areas, but the earliest pregnancy record is 4 June from eastern Vancouver Island. Newborn young weigh 1.0-1.5 grams. They grow rapidly and by three weeks are capable of flying and eating solid food. Banding studies have revealed that this bat has a long life span with some individuals living more than 30 years.

The Little Brown Myotis emerges at dusk to feed. It is an opportunistic hunter that eats a great variety of insect prey. Robert Herd's research in the southern Okanagan Valley is the only study of food habits done in the province. He found that the Little Brown Myotis hunts in the valley and nearby hills in Ponderosa Pine forests, openings of trees, and over bluffs, lakes, rivers and irrigation flumes. Aquatic insects such as midges, caddisflies and mayflies are the major prey, although beetles, moths and other kinds of flies are also taken. The diet changes seasonally in response to insect abundance, with midges predominant in spring and caddisflies and mayflies most important in summer. The Little Brown Myotis is able to adjust its hunting techniques quickly to take advantage of insect concentrations. Most prey is captured in the air and eaten while flying. After an initial feeding period of 15 to 20 minutes, individuals occupy temporary night roosts near the day retreat. Night roosts are used most often when temperatures are cool (below 15°C) a protected night roost may help the Little Brown Myotis remain active so that it can digest its meal faster.
Natural History

Summer roosts are in buildings and other man-made structures, tree cavities, rock crevices, caves and under the bark of trees. In summer the sexes live separately. Females congregate in nursery colonies that may contain hundreds or even thousands of individuals. Nursery colonies are in sites with hot (30-55°C), stable temperatures. Nursing females seem to prefer attics, but they will roost in almost any natural site that offers the environmental conditions that will promote the rapid growth of young. For example, a nursery colony of several hundred Little Brown Myotis was discovered in a small cave on the Grayling River in northern British Columbia. A hot (30°C), humid environment is maintained inside this cave by a natural hot spring.

Males rarely occupy nursery colonies. In summer they can be found roosting alone or in small colonies usually in sites that are cooler than the nurseries.

The Little Brown Myotis hibernates in caves and abandoned mines; it does not appear to hibernate in buildings. Some hibernacula in eastern Canada contain thousands of individuals. Hibernation records in British Columbia are limited to several old mines in the interior, each containing a few individuals. The whereabouts of most of the British Columbian populations in winter is unknown. Banding studies indicate that this bat will migrate 50 to 200 kilometres between hibernacula and summer roosts and if undisturbed it occupies the same sites year after year.

Before entering hibernation there is a period in late summer and early autumn when adults and young of the year make nocturnal flights through caves and mines, sites that are potential hibernacula. This swarming behaviour begins with the breakdown of the nursery colonies in late July and lasts until the bats enter hibernation. The role of swarming is not clear. It may be to familiarize young bats with the locations of potential hibernacula. Hibernation begins in September or October depending on the local climate. The Little Brown Myotis selects areas in the hibernaculum where there is high humidity (70-95%) and the temperature is above freezing (1-5°C). It may hibernate alone or in clusters. A change in temperature will waken this bat from hibernation to search for a new location in the hibernaculum. There are a few records of individuals moving to a new hibernaculum in mid winter. While hibernating, the Little Brown Myotis steadily burns up its fat reserves and loses about 25% of its weight by spring. In the interior of the province, hibernation probably lasts until April or early May, but in coastal regions this bat may arouse in late winter - it has been found feeding in coastal Oregon in mid March.


In British Columbia this bat exploits a wide range of habitats, from arid grassland and Ponderosa Pine forest to humid coastal forest and northern boreal forest. With records from sea level on the coast to 2288 metres above sea level in the Rocky Mountains (Mount Assiniboine Provincial Park), the Little Brown Myotis has the greatest altitudinal range of any of our bats. Robert Barclay's research in the Alberta Rockies indicates that males are more abundant than females at higher elevations. Similarly, at 300 to 600 metres elevation in the Cascades of western Washington, Donald Thomas observed few females and none were reproductively active.


A widespread species, the Little Brown Myotis inhabits most of North America as far north as the tree-line. In British Columbia it is found throughout the entire mainland and on several islands, including Vancouver Island and the Queen Charlotte Islands.


Three races occur in the province. M.l. alascensis, a dark subspecies that ranges from California to southeastern Alaska, is found throughout most of the province. M.l. carissima is a pale race that inhabits part of the western United States, southern Alberta and the southern dry interior of British Columbia. M.l. lucifugus, a widespread race found across eastern and central North America, is restricted to extreme northern British Columbia.


Although the Little Brown Myotis is the most widespread and one of the most abundant bats in the province, there is still much to be learned about the basic biology of this species.

Status Information

Origin StatusProvincial StatusBC List
(Red Blue List)
NativeS4YellowE (Nov 2013)
BC Ministry of Environment: BC Species and Ecosystems Explorer--the authoritative source for conservation information in British Columbia.

Additional Photo Sources

General References

Recommended citation: Author, Date. Page title. In Klinkenberg, Brian. (Editor) 2021. E-Fauna BC: Electronic Atlas of the Fauna of British Columbia [efauna.bc.ca]. Lab for Advanced Spatial Analysis, Department of Geography, University of British Columbia, Vancouver. [Accessed: 2024-07-22 7:03:30 PM]
Disclaimer: The information contained in an E-Fauna BC atlas pages is derived from expert sources as cited (with permission) in each section. This information is scientifically based.  E-Fauna BC also acts as a portal to other sites via deep links.  As always, users should refer to the original sources for complete information.  E-Fauna BC is not responsible for the accuracy or completeness of the original information.

© E-Fauna BC 2021: An initiative of the Spatial Data Lab, Department of Geography, UBC