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
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:
Anti-predator Adaptations: cryptic
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
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.
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
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 )
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 )
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:
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
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
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
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)
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.
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]
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]
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).
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]
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]
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.
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]
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]
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]
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]
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]
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]
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]
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]
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(help) 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.