Brazilian free-tailed bat (Tadarida brasiliensis)

Brazilian free-tailed bat
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Brazilian free-tailed bat fact file

Brazilian free-tailed bat description

GenusTadarida (1)

A member of the Molossidae family, the Brazilian free-tailed bat has the characteristic mouse-like tail protruding beyond the flight membrane stretched between its hind legs. Relatively plain when compared to many bats, this species has brown fur, large ears that are nearly square, and a strongly wrinkled upper lip. However, it is superbly adapted to its aerial lifestyle, having long, narrow wings with pointed tips to enable very fast flight, and long hairs on the toes to judge flight speed and turbulence. The hind legs are short and powerful, making this bat an excellent climber (3).

Also known as
guano bat, house bat, Mexican free-tailed bat.
Nyctinomus brasiliensis.
Head-body length: 95 mm (2)
Wingspan: 280 mm (3)
Tail length: 38 mm (2)
Ear length: 19 mm (2)
11 - 14 g (2)

Brazilian free-tailed bat biology

A particularly well-studied species, the Brazilian free-tailed bat exhibits some spectacular behaviour. It forms the largest warm-blooded colonies in the world, emerging to feed at dusk in huge columns of several million individuals. Their flapping wings create a sound equivalent to a white-water river and their numbers are great enough to be detected by airport and weather radars (5). Feeding for longer each night than any other bat species, it travels as far as 31 miles from the roost to the feeding grounds and uses echolocation to find its prey. The Brazilian free-tailed bat flies at up to 47 mile per hour in open spaces, foraging with fast, straight flight (7). Each bat consumes between 200 and 600 insects a night, selecting mainly moths, but also eating beetles, flying ants and leafhoppers (3). The Brazilian free-tailed bats of Texas are estimated to consume from 6,000 to 18,000 metric tons of insects each year, many of which are agricultural pests (2). At dawn, they return to their roosts where they swarm before re-entering. Thought to be a predator-avoidance tactic, the bats gather into groups at a great height above the cave, before closing their wings and dropping rapidly in one continuous stream. Predators waiting at the mouth of the cave to catch emerging bats include red-tailed hawks, owls, raccoons, opossums, skunks and snakes (5).

Mating takes place in March and shortly afterwards the females migrate to female-only maternity roosts. Most adult males do not leave the tropical and subtropical part of the range and therefore contribute nothing to rearing the young. Gestation lasts for 90 days (2) and females give birth within around 15 days of each other to a single young, known as a pup (5). The female clings to the roost with both thumbs and one or both feet to give birth, and remains attached to the pup via the umbilical cord for up to an hour while she cleans and nurses her offspring. In the first hour the young bat learns to cling to the roost wall and other bats with its hands, feet and teeth. Once stable, the female pulls away from the pup, dislodging the placenta, which hangs from the pup until it dries out and falls off several days later. During this time the number of bats in the roost doubles, and a female must locate her own pup by listening for its calls. She may land several times, eventually finding her pup by scent. Once reunited she touches the top of its head with her muzzle to confirm the bond (5).

A consequence of the enormous number of bats in a single cave is the build up of guano, or bat droppings. This nutrient-rich mixture was once commercially extracted from caves on a large scale, to be sold as fertiliser. In the early 1900s it was the largest mineral export from Texas after oil, and it continues to be sold commercially although to a lesser degree. Bat caves are widely known to contain noxious gases, but this is actually a result of carpet beetles (Dermestidae) that feed on guano and fallen bats. These beetles multiply so rapidly as a result of such a constant food supply that the whole floor of a cave may be ‘carpeted’ with them, hence their common name. They produce waste that combines with water vapour to make ammonium hydroxide which is poisonous to most animals. Bats have adapted to this potent atmosphere by lowering their metabolic rate, which causes the level of carbon dioxide dissolved in their blood to rise, thus neutralising the ammonia. Their fur, however, may become bleached to a reddish-brown colour. The first flight of the five-week-old bats is fraught with danger as they become used to their wings and echolocation system. Collisions, failed flights, and unsteady landings can result in bats falling to the cave floor, where they are stripped to the bone in minutes by the beetles (5).


Brazilian free-tailed bat range

Despite its name, the Brazilian free-tailed bat is actually widespread throughout South, Central and North America. It has fairly complex migratory habits; some populations travel from the extreme north of the range to the extreme south, whilst others remain resident year-round. The largest and most well-known populations are found in Mexico and Texas, USA. There are nine subspecies in total; all occupy different ranges and have different migration routes (3). The population is thought to total between 95 and 105 million individuals, with Bracken Cave in Texas holding between 20 and 40 million individuals alone (2).

In World War II this species was secretly investigated by the U.S. Air Force for its potential to carry tiny bombs into Japan. Bat caves were carefully guarded but the bats refused to cooperate, instead wreaking havoc in Air Force bases (5).


Brazilian free-tailed bat habitat

The Brazilian free-tailed bat is found in many different habitats from desert through pinion-juniper woodland to pine-oak forests. It inhabits areas from sea level to 3,000 metres, and roosts in limestone caves, abandoned mines, under bridges, in buildings and in hollow trees (6).


Brazilian free-tailed bat status

The Brazilian free-tailed bat is classified as Least Concern (LC) on the IUCN Red List (1) and is listed on Appendix I of the Convention on Migratory Species (4).

IUCN Red List species status – Least Concern


Brazilian free-tailed bat threats

Whilst the Brazilian free-tailed bat exists in extremely large numbers and across a great range of countries and habitat types, it is still classed as a threatened species. This is due to its reliance on a relatively low number of roost sites. With the loss of just one roost site, a large proportion of the population could be destroyed. Some significant declines have been documented, such as the population of Eagle Creek Cave, which fell from 25 million individuals in 1963 to just 30,000 individuals in 1969. These declines are not fully understood, but several threats are present, particularly from the alteration of roost sites and the use of organochlorine pesticides. Insecticides which are found in the bodies of living insects accumulate in the bodies of the bats that eat them in such large numbers, resulting in reduced reproductive success and death (7).

Rabies, a disease often associated with bats, is found in members of the Brazilian free-tailed bat population. Humans who attempt to handle bats without the proper precautions have been infected with rabies, which can be fatal. Media sensationalism of this problem has resulted in deliberate eradication attempts and roost destruction (7).


Brazilian free-tailed bat conservation

Although perhaps no species’ fate should be judged solely on its importance to humans, the Brazilian free-tailed bat is known to have an enormous impact on insect numbers, thereby contributing to both the ecology and economy of those countries that are home to it. It is crucial to continue to protect its roost sites and to educate the public and the media as to the reality of rabies and the benefits of the Brazilian free-tailed bat (7).

View information on this species at the UNEP World Conservation Monitoring Centre.

Find out more

For further information on the Brazilian free-tailed bat see:

  1. Tuttle, M.D. (1994) The Lives of Mexican free-tailed bats. Bats, 12(3): 6 – 14.
  2. Bat Conservation International at:
  3. Altringham, J.D. (1996) Bats: Biology and Behaviour. Oxford University Press, Oxford.

For more information about bats and their conservation see:

  1. Tuttle, M.D. (1994) The Lives of Mexican free-tailed bats. Bats, 12(3): 6 – 14.
  2. Bat Conservation International at:
  3. Altringham, J.D. (1996) Bats: Biology and Behaviour. Oxford University Press, Oxford.

To find out about the use of bats as bomb-carriers see:



This information is awaiting authentication by a species expert, and will be updated as soon as possible. If you are able to help please contact:


Detecting objects by reflected sound. Used for orientation and detecting and locating prey by bats and cetacea (whales and dolphins).
Accumulated droppings found where large colonies of animals such as seals, bats or birds occur; it is rich in plant nutrients, and can be used as a fertiliser for plants.
A population usually restricted to a geographical area that differs from other populations of the same species, but not to the extent of being classified as a separate species.


  1. IUCN Red List (April, 2009)
  2. The Mammals of Texas (April, 2009)
  3. Bathead (April, 2005)
  4. CMS (April, 2005)
  5. Tuttle, M.D. (1994) The Lives of Mexican free-tailed bats. Bats, 12(3): 6 - 14.
  6. Bat Conservation International (April, 2009)
  7. Texas Parks and Wildlife (April, 2009)

Image credit

Brazilian free-tailed bat  
Brazilian free-tailed bat

© Barry Mansell /

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