dcsimg

Lifespan, longevity, and ageing

provided by AnAge articles
Maximum longevity: 16.5 years (wild)
license
cc-by-3.0
copyright
Joao Pedro de Magalhaes
editor
de Magalhaes, J. P.
partner site
AnAge articles

Trophic Strategy

provided by Animal Diversity Web

M. grisescens forages over streams and reservoirs where they consume night-flying aquatic insects. Like all microchiropterans, gray bats rely on echolocation to locate their food.

Most foraging occurs within 5 meters of the water surface over which they are feeding.

Until most recently, studies focusing on the diet of gray bats were not preformed. Data on this subject are therefore preliminary. Whether gray bats are opportunistic or selective feeders is still in debate. Recent studies suggest that this species feeds selectively, but more information is needed.

Originally it was thought that gray bats fed primarily on mayflies. M. grisescens has been seen feeding in large swarms of mayflies, but this insect has not been turning up in fecal analysis in the proportion that might have been expected. It is possible that mayflies are wholly digested, thus not often seen in the fecal records.

Analysis of gray bat feces has shown that thes bats most often select moths, flies, and beetles as prey when these species are present.

Other prey includes spiders, bugs, leafhoppers, scorpionflies, lacewings, dragonflies, stoneflies, grasshoppers, thrips and wasps. Various insects occur sporadically in fecal pellet analysis.

Animal Foods: insects; terrestrial non-insect arthropods

Primary Diet: carnivore (Insectivore )

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Harriman, V. 2003. "Myotis grisescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Myotis_grisescens.html
author
Vanessa Harriman, Humboldt State University
editor
Brian Arbogast, Humboldt State University
editor
Nancy Shefferly, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Associations

provided by Animal Diversity Web

Gray bats may fall prey to howks, owls, skunks, foxes, mice, snakes, and housecats. Anti-predator adaptations include avoiding crowded cave entrances and flying more rapidly when exiting and entering the cave.

Known Predators:

  • hawks (Accipitridae)
  • owls (Strigiformes)
  • snakes (Serpentes)
  • domestic cats (Felis silvestris)
  • mice (Myomorpha)
  • skunks (Mephitinae)
  • swift foxes (Vulpes velox)
  • gray foxes (Urocyon cinereoargenteus)
  • red foxes (Vulpes vulpes)
license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Harriman, V. 2003. "Myotis grisescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Myotis_grisescens.html
author
Vanessa Harriman, Humboldt State University
editor
Brian Arbogast, Humboldt State University
editor
Nancy Shefferly, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Morphology

provided by Animal Diversity Web

M. grisecens is the largest member of its genus in the eastern United States. They weigh between 7 and 16 g and are 75 to 101 mm in length. Forearm length ranges between 40 and 46 mm. Gray bats can be distinguished from all other eastern bats by their uni-colored dorsal fur (all others have bi- or tri-colored dorsal fur). They are also the only species of Myotis in which the wing membrane connects to the foot at the ankle as opposed to connecting at the base of the first toe.

Gray bats are dark gray in color directly after they molt in July or August. Between molts, they bleach to a russet color. This difference in fur color is most apparent in females during the reproductive season (May or June).

Range mass: 7 to 16 g.

Range length: 75 to 101 mm.

Other Physical Features: endothermic ; heterothermic ; bilateral symmetry

Sexual Dimorphism: sexes alike

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Harriman, V. 2003. "Myotis grisescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Myotis_grisescens.html
author
Vanessa Harriman, Humboldt State University
editor
Brian Arbogast, Humboldt State University
editor
Nancy Shefferly, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Life Expectancy

provided by Animal Diversity Web

The maximum lifespan for gray bats is 14-15 years.

Typical lifespan
Status: wild:
14 to 15 years.

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Harriman, V. 2003. "Myotis grisescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Myotis_grisescens.html
author
Vanessa Harriman, Humboldt State University
editor
Brian Arbogast, Humboldt State University
editor
Nancy Shefferly, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Habitat

provided by Animal Diversity Web

Gray bats are restricted entirely to areas with caves or cave-like habitats. These caves are in limestone karst areas of the southeastern United States. Gray bats do not inhabit barns or other similar structures. This leads to extremely restricted nesting opportunities. Due to their requirement of unique cave types, Gray bats can only use 0.1% of available caves in the winter and 2.4% in the summer.

Ninety-five percent of the total Gray bat population hibernates in only eight or nine caves. Two are located in Tennessee, three in Missouri, one in Kentucky, one in Alabama, and one in Arkansas. The Arkansas hibernation cave houses about 250,000 Gray bats. The winter caves utilized by Gray bats have deep, vertical passages with large rooms that function as cold air traps. The temperature of these caves ranges between 6 and 11 degrees Celsius (42 and 52 degrees Fahrenheit).

As they are for the winter sites, gray bats are highly selective for caves providing specific temperature and roost conditions in the summer. These caves are warm, ranging between 14 and 25 degrees Celsius (57 and 77 degrees Fahrenheit). As an alternative to finding a cave within this temperature range, they can roost in caves with small rooms or dorms that trap the body heat of the roosting bats. Summer colonies of gray bats occupy a home range that often contains several roosting caves scattered along as much as 81 kilometers of river or lake shore. Banding studies have indicated that gray bats prefer summer caves that have a feeding area (river or other reservoir of water) not over 2 kilometers away. Despite this, they have been known to fly as far as 19 kilometers from the colony to feed.

Habitat Regions: temperate ; terrestrial

Other Habitat Features: riparian

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Harriman, V. 2003. "Myotis grisescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Myotis_grisescens.html
author
Vanessa Harriman, Humboldt State University
editor
Brian Arbogast, Humboldt State University
editor
Nancy Shefferly, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Distribution

provided by Animal Diversity Web

Myotis grisescens is widely distributed in the southeastern United States of America. The distribution of gray bats within their range has always been patchy. Gray bats inhabit the cave regions of northern Arkansas, Missouri, Kentucky, Tennessee, and Alabama. There are also occasional colonies in northwestern Florida, western Georgia, southwestern Kansas, southern Indiana, southern and southwestern Illinois, northeastern Oklahoma, northeastern Mississippi, western Virginia, and possibly western North Carolina.

Biogeographic Regions: nearctic (Native )

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Harriman, V. 2003. "Myotis grisescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Myotis_grisescens.html
author
Vanessa Harriman, Humboldt State University
editor
Brian Arbogast, Humboldt State University
editor
Nancy Shefferly, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Associations

provided by Animal Diversity Web

One bat can catch up to 3,000 insects in one night. Because of this, they play an important role in the checks and balances of nature as the primary controllers of night-flying aquatic insects.

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Harriman, V. 2003. "Myotis grisescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Myotis_grisescens.html
author
Vanessa Harriman, Humboldt State University
editor
Brian Arbogast, Humboldt State University
editor
Nancy Shefferly, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Benefits

provided by Animal Diversity Web

Insectivorous bats remove millions of insects a night, aiding in the control of these populations. Also, because of their roosting habits, inhabiting a small number of specific caves for long periods of time, these bats produce huge piles of feces on the floors of caves. Historically, this guano was used to make gunpowder during the civil war. Also, native americans used to eat these bats in stews.

Positive Impacts: food ; body parts are source of valuable material; produces fertilizer; controls pest population

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Harriman, V. 2003. "Myotis grisescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Myotis_grisescens.html
author
Vanessa Harriman, Humboldt State University
editor
Brian Arbogast, Humboldt State University
editor
Nancy Shefferly, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Benefits

provided by Animal Diversity Web

They do not adversely affect humans. Gray Bats are great!

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Harriman, V. 2003. "Myotis grisescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Myotis_grisescens.html
author
Vanessa Harriman, Humboldt State University
editor
Brian Arbogast, Humboldt State University
editor
Nancy Shefferly, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Life Cycle

provided by Animal Diversity Web

After entering the winter cave, female Gray Bats are inseminated by sexually active male bats. The females exhibit delayed fertilization. After copulating, the females hold the sperm through hibernation. Fertilization between the sperm and ova occurs when the female emerges from hibernation. Females do not reach sexual maturity until they are two years old. For their size, bats are among the world’s slowest reproducing mammal.

One offspring per sexually mature female is born in June when the colonies have migrated to their summer ranges. The period between birth and weaning is two months. During these two months there is segregation between members of the colony. The adult females and their newborns roost in maternity caves. The adult males and yearlings of both sexes roost in bachelor caves. By August, all the juveniles are flying (most are capable of flight 20-25 days after birth) and general mixing and dispersal of the colony occurs over the summer range. The growth rates of young vary with the temperature at the maternity roosts. It has been discovered that young in warmer roost situations grow more rapidly. (U.S. Fish and Wildlife Service, 1992; U.S. Fish and Wildlife Service Division of Endangered Species, 1991)

Development - Life Cycle: colonial growth

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Harriman, V. 2003. "Myotis grisescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Myotis_grisescens.html
author
Vanessa Harriman, Humboldt State University
editor
Brian Arbogast, Humboldt State University
editor
Nancy Shefferly, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Conservation Status

provided by Animal Diversity Web

M. grisescens is considered endangered by both the United States Fish and Wildlife service, according to the Endangered Species Act, and the IUCN Red List. Although CITES does not list this species of bat on Appendix I, II, or III, it is difficult to see why.

Gray bats began encountering problems in prehistorical times when tribes of Native Americans began camping and living in the entrances of caves. The smoke from their fires likely suffocated the bats. It is also thought that they were placed in stews by Native Americans.

Guano was extracted from nearly every substantial gray bat cave in the south during the Civil War. This guano was used for gunpowder, not for fertilizer, as is commonly thought. It is thought that gray bat colonies suffered some of their largest losses during the Civil War. Studies of guano deposits in formerly occupied caves shows that gray bats (a highly resilient species) were able to prosper once again in spite of these losses.

Currently, the biggest threat to gray bat populations appears to be human disturbance at hibernation and maternity colonies. The bats in the maternity colonies do not tolerate disturbance, especially when flightless newborn young are present. Thousands of baby bats may be dropped to their deaths or abandoned by panicked parents. A colony will even completely abandon a cave in the presence of excessive disturbance. This is particularly bad because so few caves are habitable for gray bats. Starvation in the winter can also be a problem. When bats are aroused during hibernation, their important fat reserves are used up more quickly. If the disturbance is intense or frequent enough the bats may starve to death.

Despite once being one of the most abundant mammals of the southeastern United States, M. grisescens has been listed as an endangered species since 1976. In 1970 the population was estimated at 2.25 million bats after a census of 120 caves. However, a census in 1976 of 22 of the 120 caves found that these colonies had declined by an average of 54 percent each.

Other factors that influence the decline of Gray Bat populations are: vandalism, cave commercialization, toxins (like organochlorine pesticides, PCB’s, and lead), natural causes like cave-ins and flooding (killing bats and destroying important habitat), loss of caves by inundation by man-made impoundments, and reduction of insect prey over streams that have been degragaded by excessive pollution and siltation. (Arkansas Game and Fish Commission, 199; Clawson and Clark, 1989)

Improper gating at cave entrances also presents a problem. Gates must allow the airflow, temperature, humidity, and amount of light entering the cave to be the same as it was prior to the gate installment. Although steel bar gates do provide excellent protection from humans, these gates may be detrimental to bats by giving predators a place to perch and wait for bats to emerge. It has also been found that bats prefer to use un-gated entrances. The alternative, if possible, would be to put up a chain link fence topped with barbedwire around the cave. This would prevent humans from entering the bats' caves, and allow the bats to fly OVER the gate, rather than through it. This would also protect them from predators perched on the gates.

Due to protective increases at high priority colony sites, declines in M. grisescens populations have been halted in some locations, and others exhibit an increase in population. Currently there are about 1.5 million gray bats in existence. Important conservation measures that have been taken to aid in the stabilization of the population, especially the acquisition of caves by the U.S. Fish and Wildlife Service. This organization is currently in control of Blowing Wind Cave in northern Alabama. This is the most important summer cave for gray bats known. Fern Cave is the largest hibernaculum for gray bats and is also under the protection of the U.S. Fish and Wildlife Service.

Additional conservation measures are needed to help M. grisescens. The purchase and protection through proper gating and restricted use of other gray bat caves is very important. Education of spelunkers and other cave visitors who may unintentionally disturb the bats is key, as well as the continuation of federal efforts to reduce pesticide use (or at least limit their lifetime in the environment).

Temperate North American bats are now threatened by a fungal disease called “white-nose syndrome.” This disease has devastated eastern North American bat populations at hibernation sites since 2007. The fungus, Geomyces destructans, grows best in cold, humid conditions that are typical of many bat hibernacula. The fungus grows on, and in some cases invades, the bodies of hibernating bats and seems to result in disturbance from hibernation, causing a debilitating loss of important metabolic resources and mass deaths. Mortality rates at some hibernation sites have been as high as 90%. While there are currently no reports of Myotis grisescens mortalities as a result of white-nose syndrome, the disease continues to expand its range in North America.

US Federal List: endangered

CITES: no special status

IUCN Red List of Threatened Species: near threatened

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Harriman, V. 2003. "Myotis grisescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Myotis_grisescens.html
author
Vanessa Harriman, Humboldt State University
editor
Brian Arbogast, Humboldt State University
editor
Nancy Shefferly, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Behavior

provided by Animal Diversity Web

As in all mammals, there are a variety of means of communication. Bats use vocalizations to communicate with each other while they are in their roosts. Mothers and infants use tactile and vocal communication. There are probably some scent cues which help mothers to recognize their young.

Echolocation is used primarily to locate food. However, communication also occurs between predator and prey through echolocation. Some insects (particularly moths) can receive the sonar pulses from the bats and fly erratically to avoid being eaten.

Communication Channels: visual ; tactile ; acoustic ; chemical

Perception Channels: visual ; tactile ; acoustic ; echolocation ; chemical

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Harriman, V. 2003. "Myotis grisescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Myotis_grisescens.html
author
Vanessa Harriman, Humboldt State University
editor
Brian Arbogast, Humboldt State University
editor
Nancy Shefferly, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Reproduction

provided by Animal Diversity Web

Information on the mating system of these animals is sparse. They are reportedly polygynous.

Mating System: polygynous

Breeding in this species occurs shortly after the bats enter their hiberation caves. After entering the winter cave, the female gray bat is inseminated. Females exhibit delayed fertilization. After copulating, a female holds the sperm through hibernation. Fertilization of ova occurs when the female emerges from hibernation.

Females do not reach sexual maturity until they are two years old. For their size, bats are among the world’s slowest reproducing mammal.

Females give birth to a single offspring in June, after migration to the summer caves has taken place. The period between birth and weaning is two months. During these two months there is segregation between members of the colony. The adult females and their newborns roost in maternity caves. The adult males and yearlings of both sexes roost in bachelor caves.

By August, all the juveniles are flying (most are capable of flight 20-25 days after birth) and general mixing and dispersal of the colony occurs over the summer range.

The growth rates of young vary with the temperature at the maternity roosts. It has been discovered that young in warmer roost situations grow more rapidly.

Breeding interval: These animals breed once per year.

Breeding season: Breeding occurs in the fall, when the bats enter their winter caves.

Range number of offspring: 1 to 1.

Average weaning age: 60 days.

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

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

Key Reproductive Features: iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; fertilization (Internal ); viviparous ; sperm-storing ; delayed fertilization

Average birth mass: 2.9 g.

Average number of offspring: 1.

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

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

As in all mammals, the mother provides milk to her growing young. Neonate gray bats are altricial. The mother attends to her young in a nursery cave. This is especially interesting, because the mother can locate her own offspring among the hundreds of baby bats which may be in the cave.

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

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Harriman, V. 2003. "Myotis grisescens" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Myotis_grisescens.html
author
Vanessa Harriman, Humboldt State University
editor
Brian Arbogast, Humboldt State University
editor
Nancy Shefferly, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Gray bat

provided by wikipedia EN

The gray bat (Myotis grisescens) is a species of microbat endemic to North America. It once flourished in caves all over the southeastern United States, but due to human disturbance, gray bat populations declined severely during the early and mid portion of the 20th century. 95% of gray bats now hibernate in only 15 caves. M. grisescens has been listed as federally endangered by the U.S. Fish and Wildlife Service since 1976,[3] and is protected under the Endangered Species Act.[2] Gray bat populations were estimated at approximately 2 million bats around the time they were placed on the Endangered Species list. By the early 1980s populations of gray bats dropped to 1.6 million. With conservation efforts in place, in 2004, gray bat populations were estimated to have reached 3.4 million.

Description

A gray bat caught in Oklahoma in 2013

M. grisescens are the largest members of their genus in the eastern United States. Of all U.S. mammals, gray bats are, perhaps, the most cave-dependent.[4] Gray bats have uni-colored dark gray fur on their backs that may bleach to a russet or chestnut brown after the molting season (July or August). Unlike in other species of Myotis, where the wing membrane connects to the toe, in M. grisescens, the wing membrane connects to the ankle. Gray bats typically weigh between 7 and 16 grams.[5] Gray bats can live up to 17 years, but only about 50% of gray bats survive to maturity. Sexual maturity occurs at about age 2.[5] Although an adult gray bat's forearm measures only about 40–46 mm,[4] Gray bats with forearm lengths of 39.5 mm (approx. 1.55 in) or less cannot fly.[6] The flight speed of the gray bat, M. grisescens, has been calculated at 20.3 km/h (12.61 mph) during migration. While foraging, gray bats have been clocked at a flying rate of anywhere between 17 km/h and 39 km/h.[7]

Annual molting occurs between early June and early August, during which gray bats eat larger amounts of hair than at other times during the activity season. During grooming, gray bats also ingest ectoparasites such as chiggers that live in their fur. Gray bats are believed to groom extensively before beginning their nightly hunt. They then spend the nighttime hours hunting and digesting.[6]

Gray bats in the wild may reach ages of at least 13–14 years (based on recapture of banded individuals), although this is considered exceptional.[8]

Distribution

Gray bats live in limestone karst areas in the southeastern United States. Summer and winter (hibernation) ranges overlap but are not identical. Hibernation occurs in caves in northern Alabama, northern Arkansas, Kentucky, Missouri, and Tennessee. During summer, the species ranges further and can be found in eastern Oklahoma and Kansas, southern Illinois and Indiana, southwestern Virginia, western North Carolina and northwestern Georgia. A very small number of records from West Virginia and Mississippi are considered to represent vagrants. Historically attested populations in Florida appear to be absent as of 2020.[8] Gray bats are cave obligate (or cave dependent) bats, meaning that with very few exceptions (in which cave-like conditions are created in man-made structures like sewers and culverts) gray bats only live in caves, not in abandoned barns or other structures as other species of bats are known to do.[5] Less than 5% of all available caves are inhabited by gray bats.[5] Thus, any disturbance to these cave habitats can be extremely detrimental to gray bat populations.

A gray bat in torpor at a hibernaculum.

Cave characteristics

Although the habitat range of the gray bat incorporates much of the southeastern United States,[9] the largest summer colonies of gray bats are located within the Guntersville Reservoir. This reservoir, found in northeastern Alabama, contains the Sauta (formerly Blowing Wind) and Hambrick caves which can accommodate over 200,000 gray bats combined.[10] Gray bats use caves differently at different times of the year. For example, populations of gray bats tend to cluster in caves known as hibernacula to prepare for winter hibernation. In contrast, their populations disperse during the spring to establish sexually segregated colonies.[9] Females form maternity colonies (also known as summer maternity roosts) while males aggregate in non-maternity, or bachelor colonies. These bachelor colonies also house yearlings of both sexes.[11] Gray bats also utilize a third type of cave, the dispersal cave, which they inhabit only during migration.[12]

For their hibernacula, gray bats prefer deep, cool caves with average temperatures ranging from 5 to 11 °C. Multiple entrances and good airflow comprise the other characteristics that gray bats find desirable. Winter hibernacula are already cold when gray bats begin arriving in September. Summer caves are usually located along rivers and have temperatures that range from 14 to 25 °C.[5] Summer caves typically contain structural heat traps (including domed ceilings, small chambers, and porous rock surfaces) that capture the metabolic heat from the clustered gray bats, allowing the nursery populations to succeed. Preferred summer colony caves are within 1 km of a body of water and are rarely further than 4 km away from a lake or major river.[5] The average roosting density of gray bats is 1828 bats/m2.[9]

Biology and behavior

Foraging

Gray bats forage over water, including streams and reservoirs, where they consume night-flying insects most of which have aquatic larval stages.[6] and in the riparian forests nearby these water sources.[12] M. grisescens activity tends to be concentrated over slower-moving water or quiet pools than areas of fast-moving water. Foraging usually occurs below treetop height but above 2m.[7] Gray bats tend to fly downstream more often than upstream, suggesting a potential preference for wider sections typical of downstream sections as opposed to upstream portions (with a tendency to be narrower). M. grisescens tend to forage over extensive ranges, averaging 12.5 km but ranging from 2.5 km to 35.4 km.[7] While gray bats have been shown to forage in small groups when prey is abundant, especially during the early hours of the night, when prey is scarce, gray bats can become territorial. Territories tend to be controlled by reproductive females. These females seem to claim the same territory year after year.[4]

Diet

Gray bats consume a variety of insects including Coleoptera (beetles), Diptera (flies), Ephemeroptera (mayflies, of which gray bats consume at least six species), Lepidoptera (moths), Neuroptera (net-winged insects), Trichoptera (caddis flies),[6] and Plecoptera (stoneflies).[12] Juveniles have a tendency to forage more in woodlands and eat more beetles than adults, perhaps they provide a greater energy reward per unit of capture effort.[12] For example, beetles provide 1900–2800 calories/g wet weight versus 800–1400 calories/g wet weight for mayflies. M. grisescens juveniles also eat a less diverse diet than adults, possibly because juveniles are more dependent on high concentrations of prey or swarming prey.[12] Gray bats are believed to be part opportunists, and part selective eaters. (Outside of captivity, gray bats are limited by the sporadic emergences of potential prey. When prey emerges, there is only an abundance of a few taxa at any given time. The available taxa change based on the time of night, the month, and the time during the activity season.) In their natural habitats, gray bats appear to attack any moving target that is of appropriate size,[6] consistent with optimal foraging theory that predicts palatable insects of an appropriate size should be eaten when encountered.[12] In captivity, under controlled laboratory conditions, however, insectivorous bats used echolocation to discriminate heavily among potential prey based on shape and texture of a target. This lack of discrimination may be because of the rapid flight of bats and the short range at which prey can be detected using echolocation, allowing bats only a fraction of a second after detection to capture prey. However, gray bats are believed to discriminate somewhat between insects when foraging in their natural habitat, consuming higher numbers of Lepidoptera, Coleoptera, Diptera, and in some populations Trichoptera, than their proportional prevalence would have otherwise indicated without selective foraging.[6] Because of this tendency to select prey while being largely opportunistic, gray bats have been dubbed ‘selective opportunists’.[12] Scientists believe that food moves quickly through the digestive tract of M. grisescens, with feces being purged from the body within 1–2 hours after ingestion.[6]

Migration, hibernation, and reproduction

Fall migration occurs in approximately the same order as spring emergence, with females departing first (early September for fall migration) and juveniles leaving last (mid-October). Gray bats may migrate as far as 500 km (310 mi) from summer caves to reach hibernation caves,[5] although based on band recovery data and the spatial distribution of summer and winter roosts, a migration range below 320 km (200 mi) appears to be the norm.[8] The annual activity period of gray bats is April to October, though female gray bats enter hibernation in September.[6]

After arriving at winter caves, copulation occurs. Females immediately enter hibernation, while males may remain active for a few more weeks.[5] Males use this extra time before entering hibernation to replenish fat reserves used during breeding.[4] Males begin hibernation by early November. During hibernation, the body temperature of gray bats drops close to the ambient temperature, allowing the body to conserve fat. These fat reserves must last the approximately six months of hibernation and spring migration.[5] Adult mortality is especially high during spring migration, as bats that do not have sufficient fat reserves have difficulties surviving the stress and energy-intensive migration period.[4] After copulation, females store sperm in their uteri, ovulating only after they have emerged from hibernation. Gestation in gray bats lasts 60 to 70 days, with birth occurring in late May and early June. Gray bat females give birth to one offspring per clutch (bout of reproduction), thus giving birth to one offspring per year. Therefore, gray bats demonstrate an iteroparous life-history strategy. The young clings to the mother for about a week, after which they remain in the maternity colony until they are able to fly. Most young take flight by four weeks of age (late June to mid-July).[5]

Energy expenditure and growth

Gray bats, as is the case in other organisms, acquire and use energy for growth and maintenance of their bodies before reaching sexual maturity, at which point much of their energy expenditure is devoted to reproductive processes. Gray bats prefer caves located near appropriate foraging sites to reduce the energy costs of flying long distances to find food.[13] Gray bats roost in large colonies to reduce the cost of temperature regulation on the individual.[14] Female bats must maintain relatively high body temperatures in comparison to the cooler temperatures of the cave during lactation, requiring large amounts of energy. During the peak lactation period, when young are roughly 20–30 days old, females may spend as many as 7 hours a night feeding. Because of the high energy demands on the females, larger roosts are more beneficial so that all may share the burden of maintaining body temperature.[4] The formation of large colonies does at some point, however, have a negative trade-off. As the size of the colony increases, intraspecific competition for food resources increase, forcing an individual to forage over a larger range. This increased foraging range will lead to greater energy expenditure, potentially reducing growth in gray bat juveniles.[14] The distance a gray bat travels from the roosting area to foraging area has been shown to be negatively correlated to the average weight of gray bats (the longer the distance the bat must fly to forage, the less the bat will weigh), lending support to the idea that long flights are energetically costly.[13]

Threats

The tendency of gray bats to form large colonies made the gray bat especially vulnerable to population decline due to both intentional and unintentional human disturbance.[9] While gray bat habitat locations were always ‘patchy,’ gray bat habitats have become increasingly more isolated and fragmented with human perturbation.[4] Suspected factors contributing to species decline include impoundment of waterways (the creation of dams, which causes flooding in former bat caves), cave commercialization, natural flooding, pesticides, water pollution and siltation, and local deforestation.[9] All North American bat species classified as endangered or threatened by the US. Fish and Wildlife service are cave dwelling species.[8] Of these species, the gray bat congregates in larger numbers at fewer winter hibernacula than any other North American bat. Approximately 95% of gray bats hibernate in 15 winter hibernacula,[8] with 31% hibernating in a single cave located in northern Alabama.[5] Because of their high population densities in appropriate habitats, gray bats serve as an important indicator species for conservation efforts.

Pesticide use

Pesticide use and manufacturing have been one of the most prevalently studied contributions to population decline of M. grisescens. One such study focused on gray bat populations of the Tennessee River area of northern Alabama where scientists and conservators noted a higher than normal gray bat mortality. In this area, since 1947, large amounts of DDTR (DDT (dichlorodiphenyltrichloroethane), DDD, and DDE) flowed through waterways from the DDT manufacturing site located on the Redstone Arsenal near Huntsville, Alabama down to the habitat area of M. grisescens, where heavy contamination of the local biota has occurred.[15] Lethal chemical concentrations of DDT in the brains of adult bats are about 1.5 times higher than in juveniles. Because M. grisescens feed on many types of insects with aquatic larval stages, it is believed that this food source may be the root of the chemical concentrations.[15] Many of the bats tested in different studies were juveniles not able to fly, and thus were likely to have only consumed milk. After concentration through lactation, a few parts per million in prey of the adult gray bat would cause mortality in these juveniles. Under conditions of rapid fat utilization, such as migratory stress or initiation of flight by juveniles, residue mobilization of harmful chemicals may occur, causing mortality.[11] Other pesticides linked with gray bat population decline include dieldrin and dieldrin's parent compound aldrin, which have also increased mortality in other bat species.[11] Even though the manufacture of DDT ceased in 1970 and the manufacture of dieldrin and aldrin in October 1974, heavy contamination of the biota persisted. Recently, however, guano samples from various habitats indicate a decline in certain detrimental chemicals. For example, guano from Cave Springs cave shows a decline of 41% in DDE (a compound related to DDT) between 1976 and 1985 and guano from Key Cave shows a decline of 67% for the same time period. However, it is unknown how long these chemicals will remain in concentrations that will cause harm to wildlife.[15]

Human disturbance

Gray bats arousing from hibernation due to human disturbance (in this instance scientists are conducting a population estimate). Gray bats may lose as much as 0.48 g of weight in the first hour of disturbance and these crucial fat reserves can not be replenished until spring emergence.

Direct human disturbance and vandalism is the major factor leading to population decline in gray bats. During the 1960s, bats were killed for entertainment purposes as they emerged from caves or were caught to be used for pranks. Many property-owners attempted to exterminate entire colonies due to unsubstantiated fears that the bats may be carrying rabies.[13] Bats that roost within 100m inside the cave and only 2m above the cave floor are especially prone to vandalism and high-intensity disturbance. Bats that roost in higher ceilings or further inside the cave are less prone to direct destruction. One study showed that caves with ceiling heights greater than 15 m above the floor were virtually protected from spelunkers.[16] Even without direct destruction, human visitation to caves can cause adverse effects on gray bat populations. Each human entry into a cave causes all bats within range of light or sound to at least partially arouse from hibernation.[5] Arousal of gray bats while they are hibernating can cause them to use up energy, lowering their energy reserves. Because these reserves must sustain the bats through hibernation and spring migration, if the bat runs out of reserves, it may leave the cave too soon, decreasing its chances of survival.[5] Each disturbance during hibernation is estimated to use energy that otherwise could sustain a gray bat through 10–30 days of undisturbed hibernation.[4] When flightless young are present in June and July, females escaping a predator or other disturbance may drop their young in the panic, leading to increased juvenile mortality.[11]

White-nose syndrome

In contrast to most other species in the genus Myotis, gray bats appear to be largely unaffected by white-nose syndrome, a fungal disease that since the mid-2000s has decimated bat populations in the United States. Continuous surveys since 2009 have indicated that gray bats may be largely resistant to the disease even when sharing roosts with infected individuals of other species.[8]

Conservation

Cave gating

Many factors play an important role in determining a viable habitat for M. grisescens. Among these are the natural characteristics of the cave entrance, physical features of the cave, and surface climate.[17] These contributing factors play an especially important role in determining the internal conditions that foster cave fauna. Because the gray bat is a cave dwelling species, its range is limited to caves whose internal conditions are favorable. Human intervention has caused a precipitous decline in the number of suitable caves for the gray bat.[18] Thus, to maximize the gray bat's range, the United States government is funding cave gating programs. Cave gating is an accepted method in protecting cave dwelling species as it limits the impact of human disturbance upon internal cave conditions. In constructing internal cave gates, several key parameters were implemented to minimize changes in the airflow through the cave and the ability of the bats to either access or leave the cave. With these limitations in mind, the internal cave gating was placed 5 to 15 meters in advance of historically critical roost areas. In addition, a 15 cm clearance between bars of the gating was allowed to ensure unobstructed flight into and out of the cave.[18] Early cave gating methods that did not account for these factors frequently led to cave abandonment. In assessing the proficiency of cave gating, two metrics were established: population dynamics before and after the construction of cave gate and initiation of emergence from the cave.[18] Population estimates were derived from the accumulation of bat guano. More guano indicated the presence of a larger population. In manipulating the emergence of gray bats from the caves under study, infrared light sources were used. Observations of the frequency of emergence of the bats from open caves and gated caves confirm that gating is not an impediment.[18] Gated entrances, however, have provided new opportunities for natural predators of gray bats. Because gates sometimes require the bats to fly slower, as well as providing hunting perches to predators within reach of emerging bats, natural predation may be increased by cave gating.[19]

Protecting populations

In their 1982 Gray Bat Recovery Plan, the US Fish and Wildlife Service laid out steps to stop decline of gray bat populations and preserve gray bat habitats. In this plan, the United States Fish and Wildlife Service proposed purchasing the caves where gray bats are known to live, and at these locations reducing human access to prevent human disturbance. To reduce human impact on gray bat populations, gating, fencing, signposting, and surveillance by law enforcement may be utilized. Because gray bats use different caves depending on the season, efforts should be focused seasonally. Rivers, reservoir shorelines, and forests should be left intact near gray bat caves to allow for adequate foraging. Any activity occurring within a 25 km radius of a major gray bat cave, such as pesticide use, herbicide use, clearing, or any activity that may result in siltation should be carefully considered and revised if necessary. Government officials and landowners of property with gray bat caves should be educated about gray bats and potentially harmful activities. Finally, the US Fish and Wildlife Service recognized the need for continuing research from the scientific community to further understand human impact on this vulnerable species.[4]

As of 2022, 70% of significant summer roosting sites and 14 of the 15 major hibernacula are considered permanently protected by a variety of means, affording year-round protection for the majority of the known population.[8]

Legal status

In the western portion of the range of M. grisescens, from 1978 to 2002, M. grisescens populations at 21 of 48 (44%) maternity caves showed a significantly increasing trend, 17 (35%) had no trend, and 10 (21%) were decreasing. A study in 2003 attempted a species-wide assessment in gray bat summer cave populations. This study found that of 76 maternity colonies, 3 (4%) were increasing, 66 (87%) had no discernible trends, and 7 (9%) had decreasing trends.[9] The Endangered Species Act requires that 90% of the most important hibernacula be protected and that populations at 75% of the most important maternity colonies be stable or increasing over a period of 5 years for the gray bat to be down-listed from endangered to threatened status. Because the range of the gray bat is so vast, and sampling techniques so varied and incomplete (thus data is somewhat unreliable when attempting to do species-wide census), gray bats are unlikely to be downgraded in the near future,[11] but total population size has rebounded by ~104% between the 1980s and 2004 (from 1.6 to 3.4 million).[5][20]

After 37 years without a single documented gray bat within the state boundaries of Mississippi, on September 20, 2004, a male gray bat was discovered in Tishomingo County in northeastern Mississippi, 42 km south of the last known location of M. grisescens before their decline and disappearance within the state of Mississippi. (Before this 2004 discovery, the only known gray bats lived at a site known as Chalk Mine, located in the northeastern portion of the county. Gray bats had last been documented at Chalk Mine in 1967.) Extensive human disturbance, including the presence of trash, smoke, and graffiti, is believed to have affected the use of the Chalk Mine by bats. While the discovery of this bat is deemed as a positive sign by conservationists, it is possible that the bat was not from a Mississippi M. grisescens population. The closest known gray bat maternal colony, located at Blowing Springs Cave, Alabama, is 90 kilometres (56 mi) northeast of where the 2004 gray bat was found, but because gray bats are known to forage over extensive areas, it is possible that this bat belonged to the Blowing Springs Cave colony.[21]

See also

References

  1. ^ Solari, S. (2018). "Myotis grisescens". IUCN Red List of Threatened Species. 2018: e.T14132A22051652. doi:10.2305/IUCN.UK.2018-2.RLTS.T14132A22051652.en. Retrieved 19 November 2021.
  2. ^ a b "Gray bat (Myotis grisescens)". Environmental Conservation Online System. U.S. Fish & Wildlife Department. Retrieved 13 April 2023.
  3. ^ a b 41 FR 17736
  4. ^ a b c d e f g h i Brady, J., T. Kunz, M. Tuttle, Ph.D., D. Wilson (July 1982). Gray Bat Recovery Plan. U.S. Fish and Wildlife Life Service.
  5. ^ a b c d e f g h i j k l m n Mitchell, W.A. & C.O. Martin (May 2002) Cave- and Crevice-Dwelling Bats on USACE Projects: Gray Bat (Myotis grisescens) Archived 2011-08-12 at the Wayback Machine.
  6. ^ a b c d e f g h Best, T.L.; B.A. Milam; T.D. Haas; W.S. Cvilikas; L.R. Saidak (1997). "Variation in diet of the Gray Bat (Myotis grisescens)". Journal of Mammalogy. 78 (2): 569–584. doi:10.2307/1382909. JSTOR 1382909.
  7. ^ a b c R.K. LaVal; R.L. Clawson; M.L. LaVal; W. Claire (1977). "Foraging Behavior and Nocturnal Activity Patterns of Missouri Bats, with Emphasis on the Endangered Species Myotis grisescens and Myotis sodalist". Journal of Mammalogy. 58 (4): 592–599. doi:10.2307/1380007. JSTOR 1380007.
  8. ^ a b c d e f g "Gray Myotis (Myotis grisescens)". U.S. Fish and Wildlife Service. Retrieved 2 September 2022.
  9. ^ a b c d e f Sherman, A.R.; Martin, C.O. (2006). Edwards, Cody W. (ed.). "Rediscovery of the Gray Bat (Myotis grisescens) in Northeastern Mississippi". Southwestern Naturalist. 51 (3): 418–420. doi:10.1894/0038-4909(2006)51[418:ROTGBM]2.0.CO;2. S2CID 86188507.
  10. ^ Boone, Madison. "Gray Bat". Encyclopedia of Alabama. Auburn University Outreach.
  11. ^ a b c d e Sasse, D.B.; Clawson, R.L.; Harvey, M.J.; Hensley, S.L. (2007). "Status of Populations of the Endangered Gray Bat in the Western Portion of its Range". Southeastern Naturalist. 6 (1): 165–172. doi:10.1656/1528-7092(2007)6[165:SOPOTE]2.0.CO;2. S2CID 85799368.
  12. ^ a b c d e f g Brack, V. Jr.; LaVal, R.K. (2006). "Diet of the Gray Myotis (Myotis grisescens): variability and consistency, opportunism, and selectivity". Journal of Mammalogy. 87 (1): 7–18. doi:10.1644/05-MAMM-A-098R1.1.
  13. ^ a b c Tuttle, M.D. (1976). "Population ecology of the Gray Bat (Myotis grisescens): Factors influencing growth and survival or newly volant young". Ecology. 57 (3): 587–595. doi:10.2307/1936443. JSTOR 1936443.
  14. ^ a b Hamilton, W. J.; W. M. Gilbert; F. H. Heppner & R. Planck (1967). "Starling roost dispersal and a hypothetical mechanism regulating rhythmic animal movement to and from dispersal centers". Ecology. 48 (5): 825–833. doi:10.2307/1933740. JSTOR 1933740. PMID 34493026.
  15. ^ a b c Bagley, F.M.; Clark, D.R. Jr. & Johnson, W.W. (1987). "Northern Alabama Colonies of the Endangered Gray Bat Myotis grisescens: Organochlorine Contamination and Mortality". Biological Conservation. 43 (3): 213–225. doi:10.1016/0006-3207(88)90114-0.
  16. ^ Tuttle, M. D. (1979). "Status, Causes of Decline, and Management of Endangered Gray Bats". The Journal of Wildlife Management. 43 (1): 1–17. doi:10.2307/3800631. JSTOR 3800631.
  17. ^ Martin, Keith W.; Leslie, David M.; Payton, Mark E.; Puckette, William L.; Hensley, Steve L. (2006). "Impacts of passage manipulation on cave climate: Conservation implications for cave-dwelling bats". Wildlife Society Bulletin. 34 (1): 137–143. doi:10.2193/0091-7648(2006)34[137:IOPMOC]2.0.CO;2. S2CID 86024277.
  18. ^ a b c d Martin, Keith W.; Leslie, David M.; Payton, Mark E.; Puckette, William L.; Hensley, Steve L. (2003). "Internal cave gating for protection of colonies of the endangered Gray Bat (Myotis grisescens)" (PDF). Acta Chiropterologica. 5 (1): 143–150. doi:10.3161/001.005.0112. S2CID 83580163. Archived from the original (PDF) on 2011-09-27. Retrieved 2011-04-22.
  19. ^ White, D. H.; Seginak, J. T. (1987). "Cave Gate Designs for Use in Protecting Endangered Bats". Wildlife Society Bulletin. 15 (3): 445–449. JSTOR 3782556.
  20. ^ Bat, G. (Myotis grisescens) 5-Year Review: Summary and Evaluation (PDF) (Report). US Fish and Wildlife Service. 2009.
  21. ^ Clark, D.R.; R.K. LaVal; D.M. Swineford (1978). "Dieldrin-Induced Mortality in an Endangered Species, the Gray Bat (Myotis grisescens)". Science. 199 (4335): 1357–1359. Bibcode:1978Sci...199.1357C. doi:10.1126/science.564550. PMID 564550.

license
cc-by-sa-3.0
copyright
Wikipedia authors and editors
original
visit source
partner site
wikipedia EN

Gray bat: Brief Summary

provided by wikipedia EN

The gray bat (Myotis grisescens) is a species of microbat endemic to North America. It once flourished in caves all over the southeastern United States, but due to human disturbance, gray bat populations declined severely during the early and mid portion of the 20th century. 95% of gray bats now hibernate in only 15 caves. M. grisescens has been listed as federally endangered by the U.S. Fish and Wildlife Service since 1976, and is protected under the Endangered Species Act. Gray bat populations were estimated at approximately 2 million bats around the time they were placed on the Endangered Species list. By the early 1980s populations of gray bats dropped to 1.6 million. With conservation efforts in place, in 2004, gray bat populations were estimated to have reached 3.4 million.

license
cc-by-sa-3.0
copyright
Wikipedia authors and editors
original
visit source
partner site
wikipedia EN