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Lifespan, longevity, and ageing

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Maximum longevity: 12 years (captivity) Observations: In the wild, these animals live at least 8 years (Brunet-Rossinni and Austad 2004). One 12 year old specimen was still alive in captivity (Richard Weigl 2005).
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Benefits

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Brazilian free-tailed bats eat large numbers of insects nightly, some of which are agricultural pests or disease vectors. Their positive economic impact on agriculture is substantial. However, agricultural pests are often exposed to pesticides through agricultural applications, which can indirectly lead to population decline. In addition, the large amount of guano produced in Brazilian free-tailed bat colonies are used for fertilizer and as a component in gunpowder.

Positive Impacts: produces fertilizer; controls pest population

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Sosnicki, J. 2012. "Tadarida brasiliensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Tadarida_brasiliensis.html
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Jessica Sosnicki, Radford University
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Associations

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Predators of Brazilian free-tailed bats include a number of raptors, such as red-tailed hawks (Buteo jamaicensis), American kestrels (Falco sparverius), great horned owls (Bubo virginianus), barn owls (Tyto alba), and Mississippi kites (Ictinia mississippiensis). Virginia opossums (Didelphis virginiana), striped skunks (Mephitis mephitis), and raccoons (Procyon lotor are among the mammalian roost predators. Snakes also prey on these bats in roosts, including eastern coachwhips (Masticophis flagellum) and eastern coral snakes (Micrurus fulviusprey). However, predation on Tadarida brasiliensis is rare; the number of bats lost due to predation is very low compared to their total population of around 100 million individuals.

Known Predators:

  • red-tailed hawks (Buteo jamaicensis)
  • American kestrels (Falco sparverius)
  • great horned owls (Bubo virginianus)
  • barn owls (Tyto alba)
  • Mississippi kites (Ictinia mississippiensis)
  • Virginia opossums (Didelphis virginiana)
  • striped skunks (Mephitis mephitis)
  • raccoons (Procyon lotor)
  • eastern coachwhips (Masticophis flagellum)
  • eastern coral snakes (Micrurus fulviusprey)

Anti-predator Adaptations: cryptic

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Sosnicki, J. 2012. "Tadarida brasiliensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Tadarida_brasiliensis.html
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Jessica Sosnicki, Radford University
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Morphology

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With brown fur and large ears, Brazilian free-tailed bats are medium-sized, with distinctive short snouts and wrinkled upper lips. The free-tailed bats, which include the genera Tadarida, Eumops, and Nycintomops, are most easily recognized by their “free-tail,” which extends well beyond the uropatagium. They have powerful legs and can climb well. Their long, narrow, pointed wings make them well-suited for rapid, direct flight. Like other temperate bat species, Brazilian free-tailed bats take advantage of daily torpor to conserve energy and may hibernate.

Adults range in size from 79 to 98 mm in length, with a tail almost half the size (31 to 41 mm). Their body mass varies seasonally and depending on maturity, adults typically weigh 7 to 12 g. Ear length is 8 to 15 mm, forearm length ranges from 37 to 41 mm, and their hindfoot measures 6 to 9 mm. The dental formula is the same as other members of the genus Tadarida: Incisors= 1/3, canines= 1/1, premolars= 2/2, molars= 3/3, with a total of 32 teeth.

Range mass: 7 to 12 g.

Range length: 79 to 98 mm.

Average wingspan: 280 mm.

Range basal metabolic rate: 1.99 to 7.31 cm3.O2/g/hr.

Other Physical Features: endothermic ; heterothermic ; bilateral symmetry

Sexual Dimorphism: sexes alike

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Sosnicki, J. 2012. "Tadarida brasiliensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Tadarida_brasiliensis.html
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Jessica Sosnicki, Radford University
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Life Expectancy

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Dental studies determined that the longest-living individual was over eight years old. Most adults have a survival rate of 70 to 80% each year, with the rate decreasing with age. Males and females have roughly equal lifespan and mortality rates. The longest reported life in captivity was 12 years old, so it is expected that they can live longer than 12 years in captivity.

Average lifespan
Status: wild:
8 years.

Average lifespan
Status: captivity:
12 years.

Average lifespan
Status: wild:
8.0 years.

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Sosnicki, J. 2012. "Tadarida brasiliensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Tadarida_brasiliensis.html
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Jessica Sosnicki, Radford University
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Habitat

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Brazilian free-tailed bats use a variety of different roost sites, including caves and man-made structures, such as bridges and attics. Caves with large rooms and high ceilings are the primary roosting habitats, although roosts also occur in hollow trees. Roosts are used for nesting, breeding, and interaction between individuals.

Habitat Regions: temperate ; terrestrial

Terrestrial Biomes: chaparral ; forest

Other Habitat Features: urban ; suburban ; caves

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Sosnicki, J. 2012. "Tadarida brasiliensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Tadarida_brasiliensis.html
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Jessica Sosnicki, Radford University
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Distribution

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Tadarida brasiliensis is a member of one of the widely distributed genera of bats in North and South America. Extensive studies on their range have yet to be completed, especially within South America; however they have been found throughout the much of the United States, Mexico, Central America, and southwestern South America, including Brazil, Chile, and Argentina. In the United States Tadarida brasiliensis is found from southern Oregon to Nevada and eastward to North Carolina and southwestern Virginia. In the last 50 to 100 years, Tadarida brasiliensis populations have declined, possibly due to a decrease in habitat, damage to roosts, and indirect consumption of pesticides.

Biogeographic Regions: nearctic (Native ); neotropical (Native )

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Sosnicki, J. 2012. "Tadarida brasiliensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Tadarida_brasiliensis.html
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Jessica Sosnicki, Radford University
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Trophic Strategy

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Brazilian free-tailed bats are aerial insectivores that use echolocation to find and consume their prey. Their diet varies based on geographical range, but mainly includes moths (Lepidoptera), beetles (Coleoptera), dragonflies (Odonata),flies (Diptera), true bugs (Hemiptera), and wasps, bees, and ants (Hymenoptera). Diet is influenced by the abundance of prey, weather conditions, metabolic demands, and lunar illumination, which can alter food availability. Brazilian free-tailed bats prey on flying insects while they are, themselves, in flight.

Animal Foods: insects

Primary Diet: carnivore (Insectivore )

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Sosnicki, J. 2012. "Tadarida brasiliensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Tadarida_brasiliensis.html
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Jessica Sosnicki, Radford University
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Tanya Dewey, University of Michigan-Ann Arbor
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Catherine Kent, Special Projects
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Associations

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Brazilian free-tailed bats are also known as guano bats. Excrement (guano) in roosts can build-up and result in tons of guano. Guano can be harvested as fertilizer and can pose a health risk in spreading diseases that are transmitted through the air (e.g., histoplasmosis). During the summer, disease transmission risk worsens, with higher temperatures and movement from within the caves generating dust clouds. Higher temperatures are also ideal for parasites and pathogens.

Brazilian free-tailed bats play host to both ecto- and endoparasites. Individuals that are part of a colony are at higher risk for being parasitized than individuals in smaller roosts. Mite, tick, chigger, flea, and beetle infections are common among Brazilian free-tailed bats, and may act as vectors for other diseases. For example, the chigger Microtrombicula merrihewi affects the nasal passages of Brazilian free-tailed bats, while other parasites affect the blood stream and digestive system. Brazilian free-tailed bats, like other mammals, are also hosts for the rabies virus and at least five other known viruses, such as the Rio Bravo virus, St. Louis encephalitis virus, Eastern equine encephalitis, Western equine encephalitis, and Japanese B encephalitis.

During the summer months, these bats significantly affect local insect populations, which makes maintaining them important to agriculture and human health by eating agricultural pests and disease vectors. More studies are needed on associations with other bat species. In Texas, Myotis velifer are most commonly seen in roosts with T. brasiliensis. Although segregated, individuals can be seen within the other’s colony especially if the roost is crowded. The flight paths of M. velifer and T. brasiliensis differ, which helps avoid competition between the two species while exiting the roost. Roosts of Brazilian free-tailed bats are used by deer mice (Peromyscus species) and squirrels.

Commensal/Parasitic Species:

  • chiggers (Microtrombicula merrihewi)
  • ticks (Ixodoidea)
  • chiggers (Trombiculidae)
  • fleas (Siphonaptera)
  • beetles (Coleoptera)
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Sosnicki, J. 2012. "Tadarida brasiliensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Tadarida_brasiliensis.html
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Jessica Sosnicki, Radford University
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Karen Francl, Radford University
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Tanya Dewey, University of Michigan-Ann Arbor
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Catherine Kent, Special Projects
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Benefits

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There is no known negative economic importance. However, histoplasmosis is a potential health concern in caves with large guano accumulations and, like other bats, Brazilian free-tailed bats can carry and transmit rabies.

Negative Impacts: injures humans (carries human disease); causes or carries domestic animal disease

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Sosnicki, J. 2012. "Tadarida brasiliensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Tadarida_brasiliensis.html
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Jessica Sosnicki, Radford University
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Karen Francl, Radford University
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Tanya Dewey, University of Michigan-Ann Arbor
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Catherine Kent, Special Projects
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Conservation Status

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Populations of Tadarida brasiliensis have declined over the last century. Some suggest this decline has been caused by disturbance and destruction of roost sites and indirect poisoning by pesticides. Tadarida brasiliensis is labeled as “near threatened” by the International Union for Conservation of Nature, with a Species Action Plan created.

US Federal List: no special status

CITES: no special status

IUCN Red List of Threatened Species: least concern

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Sosnicki, J. 2012. "Tadarida brasiliensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Tadarida_brasiliensis.html
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Jessica Sosnicki, Radford University
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Karen Francl, Radford University
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Tanya Dewey, University of Michigan-Ann Arbor
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Catherine Kent, Special Projects
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Behavior

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Brazilian free-tailed bats use echolocation as their primary mode of perception for navigation and detecting prey. They emit brief constant frequency calls as they travel, unless food or another object is detected, then they transfer to modulated frequency calls between 75 and 40 kHz. Their normal frequency ranges from 49 to 70 kHz, but can drop to 25 to 40 kHz when objects cross their flight path. Mate and intra-specific recognition is determined through the use of echolocation and through chemical, visual, and audible vocalizations. Females do not roost with their offspring, they must find their young through scent and sound recognition.

Communication Channels: visual ; tactile ; acoustic ; chemical

Perception Channels: visual ; tactile ; echolocation ; chemical

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Sosnicki, J. 2012. "Tadarida brasiliensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Tadarida_brasiliensis.html
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Jessica Sosnicki, Radford University
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Karen Francl, Radford University
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Tanya Dewey, University of Michigan-Ann Arbor
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Catherine Kent, Special Projects
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Reproduction

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Male Brazilian free-tailed bat behavior and scent-marking changes throughout the year based on the breeding season. Females gather in large numbers at maternity roosts in caves, while smaller groups can be found in tree, bridges, buildings, and other man-made structures. Males vocalize and mark territories in order to attract potential mates. Male and female free-tailed bats call to each other, singling out a mate. Once found, they move away from the group. Males aggressively mate with the female, restricting her movement by grabbing her neck, jaw, or ear. He moves onto her back, biting her neck to keep her in place. The female and male call to each other during mating. Some free-tailed bats mate multiple times, moving from mate to mate.

Mating System: polygynandrous (promiscuous)

Brazilian free-tailed bat males mature at about two years, while females mature at nine months. They are monestrous, with females having one annual estrous cycle lasting roughly five weeks during ovulation, which occurs in the spring. Male sexual activity coincides with spring female receptivity, suitable timing for mating interactions to occur. Females usually give birth to a single offspring after an 11 to 12 week gestation period. Births occur upside down and last roughly 90 seconds. It takes an additional 10 to 15 minutes for the newborn to find a nipple for feeding. The sex-ratio is typically 1:1 in pups.

Breeding interval: Breeding occurs once yearly.

Breeding season: Ovaluation lasts roughly 5 weeks in females and occurs in spring, when breeding occurs.

Average number of offspring: 1.

Range gestation period: 11 to 12 weeks.

Range time to independence: 4 to 7 weeks.

Average age at sexual or reproductive maturity (female): 9 months.

Average age at sexual or reproductive maturity (male): 2 years.

Key Reproductive Features: iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; viviparous

Average birth mass: 2.8 g.

Average number of offspring: 1.

Average age at sexual or reproductive maturity (male)
Sex: male:
547 days.

Average age at sexual or reproductive maturity (female)
Sex: female:
273 days.

Because mothers do not roost with their offspring, but rather leave them with a larger cluster of pups (a creche), she has to identify her own young through a series of calls and odors produced by the pup. Loughry and McCracken (1991) found that the scent of mothers is imprinted during early stages of development; however, pups will try latching onto any female that passes in the cluster to get fed. The young are nursed daily. They reach adult size, are weaned, and are independent in 4 to 7 weeks after birth. Brazilian free-tailed bat females have the highest milk fat content of any bat, over 28% fat, which allows their pups to grow relatively quickly.

Parental Investment: altricial ; female parental care ; pre-fertilization (Provisioning, Protecting: Female); pre-hatching/birth (Provisioning: Female, Protecting: Female); pre-weaning/fledging (Provisioning: Female, Protecting: Female)

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Sosnicki, J. 2012. "Tadarida brasiliensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Tadarida_brasiliensis.html
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Jessica Sosnicki, Radford University
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Karen Francl, Radford University
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Tanya Dewey, University of Michigan-Ann Arbor
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Catherine Kent, Special Projects
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Biology

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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 (7). 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 (6). 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 (7). 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 (7). 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 (7). 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 (7).
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Conservation

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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 (6).
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Description

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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).
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Habitat

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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 (5).
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Range

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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 (7).
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Status

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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).
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Threats

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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 (6). 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 (6).
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Comprehensive Description

provided by Smithsonian Contributions to Zoology
Tadarida brasiliensis (I. Geoffroy)

MATERIAL.—4 mandibles, 3 humeri (USNM 338511–338513). MNI = 6.
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bibliographic citation
Pregill, Gregory K. 1988. "Late Holocene fossil vertebrates from Burma Quarry, Antigua, Lesser Antilles." Smithsonian Contributions to Zoology. 1-27. https://doi.org/10.5479/si.00810282.463

Mexican free-tailed bat

provided by wikipedia EN

The Mexican free-tailed bat or Brazilian free-tailed bat (Tadarida brasiliensis) is a medium-sized bat native to the Americas, so named because its tail can be almost half its total length and is not attached to its uropatagium. It has been claimed to have the fastest horizontal speed of any animal, reaching top ground speeds over 99 mph (160 km/h).[2] It also flies the highest among bats, at altitudes around 3,300 m (10,800 ft).[3]

It is regarded as one of the most abundant mammals in North America. Its proclivity towards roosting in huge numbers at relatively few locations makes it vulnerable to habitat destruction in spite of its abundance. For instance, up to 1.5 million bats reside under just one bridge in Austin. The Texas Legislature designated the Mexican free-tailed bat the state mammal (flying) in 1995.

Taxonomy

The Mexican free-tailed bat was described as a new species in 1824 by French zoologist Isidore Geoffroy Saint-Hilaire. Geoffroy placed it in the now-defunct genus Nyctinomus with a binomial name of Nyctinomus brasiliensis.[4] The holotype had been collected in Brazil.[5] Molecular sequence data indicate T. brasiliensis's closest relatives are the sister species Sauromys petrophilus of South Africa and Tadarida aegyptiaca of Africa and South Asia. These three species form a clade believed to be about 18 million years old.[6]

Physical description

Mexican free-tailed bats are typically 9 cm (3.5 in) in length and weigh around 7–12 g (0.25–0.42 oz) with females tending to be slightly heavier than males by 1-2 grams for increased fat storage to use during gestation and nursing.[7] Their tails are almost half their total length and stretch beyond the uropatagium, giving them the name "free-tailed" bats. Their ears are wide, rounded, and large compared to their heads, nearly meeting at the front of the face, but distinctly not joined at the midline and projecting anterodorsally from just before the muzzle to the back of the head. They use their large ears to help them find prey using echolocation. T. brasiliensis is distinguished among North American Tadarida bats in possessing deep wrinkles on the upper lip and in having a Z-shaped upper third molar, which is used for grinding insects. These individuals possess canines which are larger in males than in females.[7] The wings are elongated and narrow with pointed tips, making them well-equipped for quick, straight flight patterns. Their fur color ranges from dark brown to gray. The Mexican free-tailed bat's large feet have distinct long, white bristles.[8][9] The dental formula of Tadarida brasiliensis is 1.1.1.33.1.2.3.[10]

Range and ecology

The image depicts hundreds of bats flying at dusk
Bats flying near Frio Cave in Concan, Texas

The Mexican free-tailed bat ranges from the southern half of the continental United States through most of Mexico, and through most of Central America into South America. Their range in South America is less understood where they live in the eastern Brazilian highlands and coast, the northeastern Andes, the coast of Peru and northern Chile, and the center of Argentina.[7] They are absent in much of the Amazon rainforest. They are also found in the Caribbean, and are native to all of the Greater Antilles and 11 of the Lesser Antilles.[11] The largest known colony is found at Bracken Cave, north of San Antonio, Texas, with nearly 20 million bats; the bats from this colony congregate in huge numbers at altitudes between 180 and 1,000 m (590 and 3,280 ft), and even as high as 3,000 m (9,800 ft).

Habitat

Mexican free-tailed bats roost primarily in caves. However, they also roost in buildings of any type as long as they have access to openings and dark recesses in ceilings or walls.[7] The bats can make roosting sites of buildings regardless of "age, height, architecture, construction materials, occupancy by humans and compass orientation".[7] Caves, though, need to have enough wall and ceiling space to fit millions of bats.[7] Before buildings, free-tailed bats in the Southeastern United States probably roosted in the hollows of trees such as red mangrove, black mangrove, white mangrove, and cypress. However, most bats in Florida seem to prefer buildings and other man-made structures over natural roosts.[7] Caves in Florida tend to be occupied mostly by the southeastern myotis. Caves in Florida tend to have pools of water on the floor and the free-tailed bats do not need as much relative humidity as the southeastern myotis.[7]

Migration

The image depicts hundreds of bats flying at dusk
Mexican free-tailed bats, emerging from Carlsbad Caverns, Carlsbad Caverns National Park, New Mexico

Mexican free-tailed bats in southeastern Nevada, southwestern Utah, western Arizona, and southeastern California come together to migrate southwest to southern California and Baja California.[7] Bats in southeastern Utah, southwestern Colorado, western New Mexico, and eastern Arizona travel through the western edge of the Sierra Madre Oriental into Jalisco, Sinaloa, and Sonora. Some bats that summer in Kansas, Oklahoma, eastern New Mexico, and Texas migrate southward to South Texas[12] and Mexico.[7] Some bat populations in other areas of North America do not migrate, but are residents and may make seasonal changes in roost sites.[7] While this migration is extremely extensive, a way must exist for these bats to continuously congregate in the same roosts every year. T. brasiliensis bats have copious numbers of sebaceous glands covering their entire bodies. These glands leave a trace of a lasting scent to which other bats are sensitive. This odor is crucial to marking habitual roosts.[13]

The image depicts hundreds of bats flying from under the Congress Avenue Bridge at dusk
Dusk emergence of bats at the Congress Avenue Bridge in Austin, Texas

Bats ranging eastward from East Texas do not migrate, but local shifts in roost usage often occur seasonally.[7] Also, a regional population that ranges from Oregon to California, has a year-round residence.

Diet

Mexican free-tailed bats are primarily insectivores. They hunt their prey using echolocation. The bats eat moths, beetles, dragonflies, flies, true bugs, wasps, and ants. They usually catch flying prey in flight.[14] Large numbers of Mexican free-tailed bats fly hundreds of meters above the ground in Texas to feed on migrating insects.[15] The consumption of insects by these bats can be quite significant.[16][17]

The onset of evening emergence from caves and the end of returns at dawn tend to correlate with sunset and sunrise, respectively, with dawn returns ending increasingly later in correlation to sunrise throughout the summer season. Reproductive females tended to emerge earlier in the evening and return later at dawn to gather the extra nutrients they require for reproduction and offspring care.[18] T. brasiliensis bats spend around 60% of their active time foraging while aerial, mostly hunting at heights of 6–15 m (20–49 ft).[7] Individuals will fly 50 km (31 mi) in one night to reach foraging areas. The loose, wrinkled skin around the mouth is thought to aid in expanding the mouth during flight to catch insects. T. brasiliensis requires free water sources to maintain water balance: individuals from the arid environment of New Mexico tend to have thicker renal tissue layers compared to T. brasiliensis from the less arid California, revealing that urine concentrating abilities and water use varies geographically with aridity.[19]

Health and mortality

One individual bat was recorded to have lived 8 years, based on dentition.[20] Predators of the bat include large birds such as red-tailed hawk, American kestrels, great horned owls, barn owls, and Mississippi kites.[7][21] Mammal predators include Virginia opossums, striped skunks, and raccoons.[7] Snakes such as eastern coachwhips and gopher snakes may also prey on them, but at a lesser extent. Certain types of beetles prey on neonate and juvenile bats that have fallen to the ground.[7] This species seems to have a low incidence of rabies, at least in the United States.[7] They do, however, contain certain pesticides.[7]

White-nose syndrome (WNS) caused by infection by the fungus P. destructans has increased in prevalence since 2006, mostly affecting species of bats that roost underground such as the little brown bat. The fungus, now suspected to have spread from accidental transportation by human cave workers, is thought to cause frequent arousals during bat hibernation, causing an individual to use fat stores much more quickly and die of starvation before the end of winter. WNS can affect T. brasiliensis, but has yet to be greatly introduced to their habitat due to their preference for more arid caves. WNS has low prevalence in the subtropical and tropical regions where T. brasiliensis resides.[22]

Behavior

A male displays and sings in the presence of females (watch in slow motion).

Mexican free-tailed bats are nocturnal foragers and begin feeding after dusk. They travel 50 km in a quick, direct flight pattern to feed. This species flies the highest among bats, at altitudes around 3,300 m (10,800 ft).[23] Bats appear to be most active in late morning and afternoon between June and September.[24] Free-tailed bats are more active in warm weather.[25]

The species has been measured at a ground speed of 160 km/h (99 mph), measured by an aircraft tracking device.[26] The measurement methodology did not simultaneously record wind speed and ground speed, so the observations could have been affected by strong local gusts, and the bat's maximum air speed remains uncertain.[27]

Guano and ammonia

Among bats that roost in great, concentrated numbers, T. brasiliensis roosts produce large quantities of urine and guano; from 22 to 99 metric tons per cave and over 18,700 metric tons are produced annually. The concentrated waste generates high levels of toxic ammonia in the air of a cave. T. brasiliensis individuals have genetic adaptation for withstanding or countering these high levels of ammonia. The bats’ content of CO2 and protein in respiratory mucus and CO2 dissolved in blood plasma increase with increasing levels of dissolved ammonia, providing the bats with a buffer against pH change. This allows the bats to filter out a large majority of inhaled ammonia before it reaches toxic levels in the blood. T. brasiliensis bats are thought to swarm in spiraling motions within caves to ventilate ammonia and renew the air.[7]

Echolocation

Mexican free-tailed bats use echolocation for navigation and detecting prey. Traveling calls are of a brief but constant frequency. However, they switch modulated frequency calls between 40 and 75 kHz if they detect something.[28] Typically, the frequency range of their echolocation is between 49 and 70 kHz, but can be between 25 and 40 kHz if something crosses their path while in flight.[28]

On 6 November 2014, Aaron Corcoran, a biologist at Wake Forest University, North Carolina, reported online in Science that his team and he had detected Mexican free-tailed bats emitting ultrasonic vocalizations that had the effect of jamming the echolocation calls of a rival bat species hunting moths. The ‘jamming’ call led to an increased chance of the rival missing its prey, which the Mexican free-tailed bat was then able to eat itself. Earlier researchers had discovered some 15 types of social calls made by Mexican free-tailed bats and reported that they could adjust their calls to avoid interfering with others in range of their calls.[29][30]

Mating and reproduction

The image depicts bats hanging from the wall of a cave
Free-tailed bats roosting at a cave in the Bahamas

During the breeding season, females aggregate into maternity roosts. The size of these roosts depends on the environment, with caves having the larger roosts. Mating can occur in an aggressive or passive form. In the aggressive form, the male controls the female's movements, keeping her away from the other bats in the roost.[31] He also tends to vocalize when mating. During passive copulation, the males simply flies to a female in her roost and quietly mounts her with no resistance. This species is a promiscuous breeder and both sexes copulate with multiple partners.[31] Females become sexually mature at about 9 months, while males take even longer, at two years. Females enter estrus once a year, which typically lasts five weeks in the spring. The gestation period of the bat lasts 11–12 weeks, with only one young being born. A number of pups are left in "creches", while their mothers roost elsewhere. The female uses vocalizations and scent to identify her pup. The mother imprints her scent on the young early on.[32] However, young try to steal a suckle from any female that passes through the cluster. Through examining the genotypes of female-pup nursing pairs sampled from colonies in Texas, it has been measured that nursing is partially selective along genetic lines, with approximately 17% of mothers nursing pups that were not their offspring, ostensibly due to the difficulty of consistently locating and selectively nursing their own pups in extremely large colonies.[33] A mother will nurse her young daily, and by 4–7 weeks old they are full grown, fully weaned, and independent.[34]

Conservation

Though abundant and widespread, some local populations have prompted protection and conservation efforts. For instance, during the spring and summer, one of the largest Mexican free-tailed bat populations inhabits Cueva de la Boca, a cave near Monterrey, Mexico. In 2006, the Mexican environmental conservation NGO, Pronatura Noreste, purchased the property. Because of a reduction by more than 95% of the original 20 million bat population to 600,000, as a result of vandalism, pollution, and uncontrolled tourism, the organization decided to buy the property to place it under conservation. Other species of high ecological value that inhabit the cavern are also being protected. Similarly, Bat Conservation International bought Bracken Cave from private ownership in 1992. BCI planned to revert any land changes that were a result of farming or ranching in order to conserve the biodiversity and wildlife there. Preserving the land around Bracken Cave was important, as it is home to the world's largest bat colony, and any human encroachment would be detrimental to their population. BCI also protects the land from artificial light pollution, which can distress the bats.[35][36]

Economic importance

In Austin, Texas, a colony of Mexican free-tailed bats summers (they winter in Mexico) under the Congress Avenue Bridge 10 blocks south of the Texas State Capitol. It is the largest urban colony in North America, with an estimated 1,500,000 bats.[37] Each night they eat 10,000 to 30,000 lb (4,500 to 13,600 kg) of insects. Each year, they attract 100,000 tourists who come to watch them. In Houston, Texas, a colony is living under the Waugh Street Bridge over Buffalo Bayou. It is the home to 250,000 bats and also attracts viewers. The Mexican free-tailed bat is the official flying mammal of the state of Texas.[38]

Hundreds of tons of guano were mined in Texas annually between 1900 and 1980. In the early 20th century, bat guano was Texas' largest mineral export, before oil. In 1863, a gun powder factory opened near San Antonio, the saltpeter of which was provided by local guano mines. [39]

See also

  • Bat bomb, an experimental incendiary weapon that used Mexican free-tailed bats as a dispersal mechanism

References

  1. ^ Barquez, R.; Diaz, M.; Gonzalez, E.; Rodriguez, A.; Incháustegui, S.; Arroyo-Cabrales, J. (2015). "Tadarida brasiliensis". IUCN Red List of Threatened Species. 2015: e.T21314A22121621. doi:10.2305/IUCN.UK.2015-4.RLTS.T21314A22121621.en. Retrieved 27 September 2022.
  2. ^ "Speedy Bat Smashes Speed Record".
  3. ^ Williams, T. C.; Ireland, L. C.; Williams, J. M. (1973). "High Altitude Flights of the Free-Tailed Bat, Tadarida brasiliensis, Observed with Radar". Journal of Mammalogy. 54 (4): 807. doi:10.2307/1379076. JSTOR 1379076.
  4. ^ Geoffroy, I. (1824). "Par M. Isidore Geoffroy Saint-Hilaire. Lu á la Société d'histoire naturelle de Paris le vendredi 5 mars 1824" [By Mr. Isidore Geoffroy Saint-Hilaire. Read at the Natural History Society of Paris on Friday, March 5, 1824]. Annales des sciences naturelles (in French). 1: 342–343.
  5. ^ Smith Miller, Gerrit; Rehn, James A. G. (1901). Systematic Results of the Study of North American Land Mammals to the Close of the Year 1900. Society of Natural History. p. 271.
  6. ^ Ammerman, LK; Lee, DN; Tipps, T (2012). "First molecular insights into the evolution of free-tailed bats in the subfamily Molossinae (Molossidae, Chiroptera)". Journal of Mammalogy. 93 (1): 12–28. doi:10.1644/11-mamm-a-103.1.
  7. ^ a b c d e f g h i j k l m n o p q r s Wilkins, K. (1989). "Tadarida brasiliensis". Mammalian Species (331): 1–10. doi:10.2307/3504148. JSTOR 3504148.
  8. ^ "Brazilian Free-tailed Bat (Tadarida brasiliensis)". Archived from the original on 11 May 2000.
  9. ^ https://upload.wikimedia.org/wikipedia/commons/b/b9/Mexican_free-tailed_bat_%288006850693%29.jpg
  10. ^ Reid, F. (2006). A field guide to mammals of North America, north of Mexico. Vol. 4. Houghton Mifflin Harcourt. p. 136.
  11. ^ Baker, R. J., Genoways, H. H. (1978). "Zoogeography of Antillean bats", pp. 53–97 in Zoogeography in the Caribbean, F. B. Gill (ed.). Philadelphia: Acad
  12. ^ Glass BP (1982). "Seasonal movements of Mexican free-tail bats Tadarida brasiliensis mextcana banded in the Great Plains". Southwestern Nat. 27 (2): 127–133. doi:10.2307/3671136. JSTOR 3671136.
  13. ^ Glass, Bryan P. (1982). "Seasonal Movements of Mexican Freetail Bats Tadarida brasiliensis mexicana Banded in the Great Plains". The Southwestern Naturalist. 27 (2): 127–133. doi:10.2307/3671136. JSTOR 3671136.
  14. ^ McWilliams, Lisa A. (2005). "Variation in Diet of the Mexican Free-Tailed Bat (Tadarida brasiliensis mexicana)". Journal of Mammalogy. 86 (3): 599–605. doi:10.1644/1545-1542(2005)86[599:VIDOTM]2.0.CO;2. S2CID 86220457.
  15. ^ McCracken, G. F.; Gillam, E. H.; Westbrook, J. K.; Lee, Y. F.; Jensen, M. L.; Balsley, B. B. (2008). "Brazilian free-tailed bats (Tadarida brasiliensis: Molossidae, Chiroptera) at high altitude: Links to migratory insect populations". Integrative and Comparative Biology. 48 (1): 107–18. doi:10.1093/icb/icn033. PMID 21669777.
  16. ^ Corrigan, Robert. Do Bats Control Mosquitoes? Archived 2 April 2015 at the Wayback Machine texasmosquito.org
  17. ^ Animal Fact Sheet: Mexican Free-Tailed Bat. Desert Museum.
  18. ^ Lee, Y. F.; McCracken, G. F. (2001). "Timing and variation in the emergence and return of Mexican free-tailed bats, Tadarida brasiliensis mexicana" (PDF). Zoological Studies. 40 (4): 309–316.
  19. ^ Bassett, JE (1982). "Habitat aridity and intraspecific differences in the urine concentrating ability of insectivorous bats". Comparative Biochemistry and Physiology. 72 (4): 703–708. doi:10.1016/0300-9629(82)90152-9. PMID 6126307.
  20. ^ Gannon, M., A. Kurta, A. Rodriquez-Duran, M. Willig. (2005). Bats of Puerto Rico. Jamaica. The University of the West Indies Press.
  21. ^ Mikula, P.; Morelli, F.; Lučan, R. K.; Jones, D. N.; Tryjanowski, P. (2016). "Bats as prey of diurnal birds: a global perspective". Mammal Review. 46 (3): 160. doi:10.1111/mam.12060.
  22. ^ Fenton, B (2012). "Bats and white-nose syndrome". PNAS. 109 (18): 6794–6795. Bibcode:2012PNAS..109.6794F. doi:10.1073/pnas.1204793109. PMC 3344961. PMID 22517743.
  23. ^ Williams, T. C.; Ireland, L. C.; Williams, J. M. (1973). "High Altitude Flights of the Free-Tailed Bat, Tadarida brasiliensis, Observed with Radar". Journal of Mammalogy. 54 (4): 807. doi:10.2307/1379076. JSTOR 1379076.
  24. ^ Svoboda, P. L.; Choate, J. R. (1987). "Natural History of the Brazilian Free-Tailed Bat in the San Luis Valley of Colorado". Journal of Mammalogy. 68 (2): 224. doi:10.2307/1381461. JSTOR 1381461.
  25. ^ Allen, L. C.; Turmelle, A. S.; Mendonça, M. T.; Navara, K. J.; Kunz, T. H.; McCracken, G. F. (2009). "Roosting ecology and variation in adaptive and innate immune system function in the Brazilian free-tailed bat (Tadarida brasiliensis)" (PDF). Journal of Comparative Physiology B. 179 (3): 315–23. doi:10.1007/s00360-008-0315-3. PMC 7087743. PMID 19002470.
  26. ^ McCracken, Gary F.; Safi, Kamran; Kunz, Thomas H.; Dechmann, Dina K. N.; Swartz, Sharon M.; Wikelski, Martin (9 November 2016). "Airplane tracking documents the fastest flight speeds recorded for bats". Royal Society Open Science. 3 (11): 160398. Bibcode:2016RSOS....360398M. doi:10.1098/rsos.160398. PMC 5180116. PMID 28018618.
  27. ^ Photopoulos, Julianna (9 November 2016). "Speedy bat flies at 160km/h, smashing bird speed record". New Scientist. Retrieved 11 November 2016. But not everyone is convinced. Graham Taylor at the University of Oxford says that errors in estimating bat speed by measuring the distance moved between successive positions could be huge. "So I think it would be premature to knock birds off their pedestal as nature's fastest fliers just yet," he says."These bats are indeed flying very fast at times, but this is based on their ground speed," says Anders Hedenström at the University of Lund in Sweden. "Since they did not measure winds at the place and time where the bats are flying, one can therefore not exclude that the top speeds are not bats flying in a gust."
  28. ^ a b Gillam, Erin H.; McCracken, Gary F. (2007). "Variability in the echolocation of Tadarida brasiliensis: Effects of geography and local acoustic environment". Animal Behaviour. 74 (2): 277. doi:10.1016/j.anbehav.2006.12.006. S2CID 53174117.
  29. ^ Morell, Virginia (6 November 2014). "Holy blocked bat signal! Bats jam each other's calls". new.sciencemag.org. Retrieved 8 November 2014.
  30. ^ Hogenboom, Melissa (7 November 2014). "Bats sabotage rivals' senses with sound in food race". BBC News. Retrieved 8 November 2014.
  31. ^ a b Keeley, Annika T. H.; Keeley, Brian W. (2004). "The Mating System of Tadarida brasiliensis (Chiroptera: Molossidae) in a Large Highway Bridge Colony". Journal of Mammalogy. 85: 113–119. doi:10.1644/BME-004.
  32. ^ Loughry, W. J.; McCracken, G. F. (1991). "Factors Influencing Female-Pup Scent Recognition in Mexican Free-Tailed Bats". Journal of Mammalogy. 72 (3): 624. doi:10.2307/1382150. JSTOR 1382150.
  33. ^ McCracken, Gary F. (9 March 1984). "Communal Nursing in Mexican Free-Tailed Bat Maternity Colonies". Science. 223 (4640): 1090–1091. Bibcode:1984Sci...223.1090M. doi:10.1126/science.223.4640.1090. PMID 17830157. S2CID 206572086.
  34. ^ Kunz, Thomas H.; Robson, Simon K. (1995). "Postnatal Growth and Development in the Mexican Free-Tailed Bat (Tadarida brasiliensis mexicana): Birth Size, Growth Rates, and Age Estimation" (PDF). Journal of Mammalogy. 76 (3): 769. doi:10.2307/1382746. JSTOR 1382746.
  35. ^ "Bracken Cave Preserve - Texas Hill Country Region". Texas Parks and Wildlife Department. Texas Parks and Wildlife Department. Retrieved 24 September 2020.
  36. ^ "Preserving Bracken Cave and the largest bat colony in the world". www.batcon.org. Bat Conservation International.
  37. ^ "Congress Avenue Bridge". Congress Avenue Bridge Bat Colony. Archived from the original on 12 November 2008.{{cite web}}: CS1 maint: bot: original URL status unknown (link)
  38. ^ "Texas State Symbols". Texas State Library and Archives Commission.
  39. ^ https://www.batcon.org/article/the-lives-of-mexican-free-tailed-bats/. {{cite web}}: Missing or empty |title= (help)

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Mexican free-tailed bat: Brief Summary

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The Mexican free-tailed bat or Brazilian free-tailed bat (Tadarida brasiliensis) is a medium-sized bat native to the Americas, so named because its tail can be almost half its total length and is not attached to its uropatagium. It has been claimed to have the fastest horizontal speed of any animal, reaching top ground speeds over 99 mph (160 km/h). It also flies the highest among bats, at altitudes around 3,300 m (10,800 ft).

It is regarded as one of the most abundant mammals in North America. Its proclivity towards roosting in huge numbers at relatively few locations makes it vulnerable to habitat destruction in spite of its abundance. For instance, up to 1.5 million bats reside under just one bridge in Austin. The Texas Legislature designated the Mexican free-tailed bat the state mammal (flying) in 1995.

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