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Lifespan, longevity, and ageing

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Maximum longevity: 6 years (wild)
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Behavior

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Like most other bats, greater sac-winged bats use echolocation to perceive their environment and forage. The frequency ranges of their foraging calls are between 42 and 50 kHz. In addition to echolocation vocalizations, S. bilineata males use vocalizations along with olfactory and visual cues to attract mates to their harem. Males perform hovering displays when a female enters their territory and they produce complex songs as both territorial and courtship displays. Territorial song bouts last up to 4 seconds and consist of 20 to 50 elements. These songs are produced occasionally throughout the day and more frequently at dawn and dusk, when the colony is most active. Courtship songs are more complex than territorial songs and may last for minutes or up to an hour. These songs are usually at a frequency of above 20 kHz, with tonal elements known as trills composed of a rippled modulation of the basal frequency modulation. The trill element of the courtship song varies from male to male, suggesting it may play a role in female choice and individual identification. Males also use scents with females, with perfume displays increasing in frequency prior to and during the mating season. Females respond to scent displays with social vocalizations or by waving a folded forearm at the male. Recent chemical analysis by gas chromatography has shown that S. bilineata and its sister species Saccopteryx leptura have species specific male scents. Female choice experiments confirm that females prefer the scent of their own species over those of sister species.

Communication Channels: visual ; acoustic ; chemical

Other Communication Modes: pheromones

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

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Luzynski, K. and E. Sluzas 2009. "Saccopteryx bilineata" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Saccopteryx_bilineata.html
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Ken Luzynski, University of Michigan-Ann Arbor
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Emily Sluzas, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Tanya Dewey, Animal Diversity Web
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Conservation Status

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Saccopteryx bilineata is relatively abundant in its range and quite tolerant of habitat alteration, often using man made structures as roosts.

US Federal List: no special status

CITES: no special status

State of Michigan List: no special status

IUCN Red List of Threatened Species: least concern

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Luzynski, K. and E. Sluzas 2009. "Saccopteryx bilineata" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Saccopteryx_bilineata.html
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Ken Luzynski, University of Michigan-Ann Arbor
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Emily Sluzas, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Tanya Dewey, Animal Diversity Web
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Benefits

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Where Saccopteryx bilineata occurs with other species, particularly Desmodus rotundus, a bacteria (Histoplasmosis capsulatum) that causes respiratory problems has been detected at high levels in the droppings.

Negative Impacts: injures humans (carries human disease)

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Luzynski, K. and E. Sluzas 2009. "Saccopteryx bilineata" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Saccopteryx_bilineata.html
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Ken Luzynski, University of Michigan-Ann Arbor
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Emily Sluzas, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Tanya Dewey, Animal Diversity Web
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Benefits

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Saccopteryx bilineata is the most abundant insectivorous bat species in some regions of the neotropics. Although no specific information is available on the quantity of insects consumed by S. bilineata, it is likely that they play a role in controlling insect populations, as demonstrated in several recent studies of insectivorous bats in the tropics.

Positive Impacts: controls pest population

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Luzynski, K. and E. Sluzas 2009. "Saccopteryx bilineata" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Saccopteryx_bilineata.html
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Ken Luzynski, University of Michigan-Ann Arbor
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Emily Sluzas, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Tanya Dewey, Animal Diversity Web
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Associations

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Greater sac-winged bats are insect predators. If these bats occur in high densities or with many other species, the accumulation of their feces may be a significant source of nutrients to the soil and plants under their roost. They also significantly impact populations of insects and are parasitized by a number of internal and external parasites.

Commensal/Parasitic Species:

  • streblid flies (Euctenodes) (ectoparasite)
  • trombiculid mites (Eutrombicula goldii) (ectoparasite)
  • trombiculid mites (Trombicula saccopteryx) (ectoparasite)
  • trombiculid mites (Trombicula vesperuginis) (ectoparasite)
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Luzynski, K. and E. Sluzas 2009. "Saccopteryx bilineata" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Saccopteryx_bilineata.html
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Ken Luzynski, University of Michigan-Ann Arbor
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Emily Sluzas, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Tanya Dewey, Animal Diversity Web
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Trophic Strategy

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Saccopteryx bilineata is strictly insectivorous. Diet studies in Costa Rica and Trinidad have found S. bilineata consuming primarily beetles and flies whereas other studies have found frequent consumption of lepidopterans. Specialization on one prey type has not been observed. Greater sac-winged bats forage 3 to 8 m from the ground using straight-line chases and sharp turns before obstacles. Foraging occurs for 2 to 3 hours after dusk with 20 to 30 minutes of effort in each foraging bout. Greater sac-winged bats use relatively long, paired search phase calls with the first call lasting 5.1 to 6.7 ms and the second call, 2 to 3 kHz lower, lasting 4.8 to 6.0 ms. Calls are characterized by a slight rise in frequency at the beginning of a pulse, followed by an extended constant frequency portion, ending with a slight decrease in frequency. Calls vary in frequency throughout the geographic range of Saccopteryx bilineata, from 47 to 50 kHz recorded in a Costa Rican population and 43 to 45 kHz documented in a population in Belize. Colonies of S. bilineata have exclusive foraging ranges, with most individuals from one colony sharing a foraging area. Although individuals from a colony forage near each other, they forage in a solitary manner, unlike the group foraging of closely related Saccopteryx leptura. Studies in Costa Rica showed that foraging activity of S. bilineata is positively correlated with phenological activity and presumably insect abundance in forested habitat. Due to the highly seasonal nature of food sources, S. bilineata changes foraging patches every 5 to 10 weeks.

Animal Foods: insects

Primary Diet: carnivore (Insectivore )

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Luzynski, K. and E. Sluzas 2009. "Saccopteryx bilineata" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Saccopteryx_bilineata.html
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Ken Luzynski, University of Michigan-Ann Arbor
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Emily Sluzas, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Tanya Dewey, Animal Diversity Web
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Distribution

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The northern boundary of the distribution of Saccopteryx bilineata occurs in central Mexico, with capture records from Jalisco and Veracruz. The range extends south to central South America including northern Bolivia, Guyana, Suriname, Guyane, and eastern Brazil, but excluding Paraguay. The range of Saccopteryx bilineata extends as far south as Rio de Janeiro on the eastern coast of South America. Saccopteryx bilineata has also been found on Antillean islands, including Trinidad and Tobago.

Biogeographic Regions: neotropical (Native )

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Luzynski, K. and E. Sluzas 2009. "Saccopteryx bilineata" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Saccopteryx_bilineata.html
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Ken Luzynski, University of Michigan-Ann Arbor
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Emily Sluzas, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Tanya Dewey, Animal Diversity Web
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Habitat

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Saccopteryx bilineata is found throughout lowland neotropical forests, but it also makes use of man-made structures and can be found in disturbed habitats and plantations. Most specimens have been found near water sources. This species roosts under bridges, in caves, in cliff crevices, and in hollow trees. Saccopteryx bilineata has been recorded roosting with many other bat species; however, it tends to roost in more well-lit places than most other bats.

Range elevation: 0 to 575 m.

Habitat Regions: tropical ; terrestrial

Terrestrial Biomes: rainforest

Other Habitat Features: urban ; suburban ; caves

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Luzynski, K. and E. Sluzas 2009. "Saccopteryx bilineata" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Saccopteryx_bilineata.html
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Ken Luzynski, University of Michigan-Ann Arbor
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Emily Sluzas, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Tanya Dewey, Animal Diversity Web
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Life Expectancy

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The record lifespan for Saccopteryx bilineata is 6 years. No records of bats in captivity are available, most likely due to the difficulty of keeping aerial insectivores with large home ranges.

Range lifespan
Status: wild:
6 (high) years.

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Luzynski, K. and E. Sluzas 2009. "Saccopteryx bilineata" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Saccopteryx_bilineata.html
author
Ken Luzynski, University of Michigan-Ann Arbor
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Emily Sluzas, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Tanya Dewey, Animal Diversity Web
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Morphology

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Saccopteryx bilineata has dark pelage with 2 whitish longitudinal stripes running down the dorsal side of the body from each shoulder to the rump. This species has a simple muzzle without a leaf-like nasal structure or inflation of the rostrum. The black color of S. bilineata fades to deep brown as it becomes worn. The ventral surface is brown to gray. The uropatagium is slightly hairy. Total length varies from 73 to 78 mm, the length of the tail is on average 21.6 mm, the length of the ear ranges between 17.51 and 17.96 mm, and the length of the forearm is between 47.13 and 49.16 mm. Saccopteryx bilineata body mass ranges from 8.5 to 9.3 g, females are generally slightly larger than males. The skull has a large post-orbital process and premaxillilaries that are incomplete and not attached medially. This species has 32 teeth with a dental formula of 1/3, 1/1, 2/2, 3/3. Cranial length ranges from 13.2 to 15.7 mm. The dorsal stripes are pronounced in S. bilineata and serve as a distinguishing feature when comparing this bat to Saccopteryx canescens. Saccopteryx bilineata is larger and has a darker pelage than Saccopteryx leptura, which is lighter brown. As with all members of this genus, this species has wing sacs which help to distinguish it from superficially similar bats of the genus Rhynchonycteris.

Range mass: 8.5 to 9.3 g.

Range length: 73 to 76 mm.

Range basal metabolic rate: 1.31 to 2.41 cm3.O2/g/hr.

Average basal metabolic rate: 1.86 cm3.O2/g/hr.

Other Physical Features: endothermic ; homoiothermic; bilateral symmetry

Sexual Dimorphism: female larger

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Luzynski, K. and E. Sluzas 2009. "Saccopteryx bilineata" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Saccopteryx_bilineata.html
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Ken Luzynski, University of Michigan-Ann Arbor
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Emily Sluzas, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Tanya Dewey, Animal Diversity Web
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Associations

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No specific data are available on predation of S. bilineata. Possible predators which have been recorded preying on other bat species include snakes, owls, and small carnivores. Greater sac-winged bats are cryptically colored when roosting and are active at night, protecting them from some predation.

Anti-predator Adaptations: cryptic

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Luzynski, K. and E. Sluzas 2009. "Saccopteryx bilineata" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Saccopteryx_bilineata.html
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Ken Luzynski, University of Michigan-Ann Arbor
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Emily Sluzas, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Tanya Dewey, Animal Diversity Web
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Reproduction

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The Saccopteryx bilineata mating system is polygynous, in which males defend harems of 3 to 5 females from other males. Since females are larger than males, they control copulation and are often more agonistic toward males than accepting. Therefore, males principally maintain a roosting and foraging territory in order to attract females. Males also use a suite of olfactory, visual, and ultrasonic vocal displays to attract and retain females. Males spend much of the afternoon cleaning the sacs on their wing membranes with saliva and urine. A genital secretion is then collected with the chin and applied to the wing sacs. Once the sacs are prepared, a male performs flight displays in which it hovers over females in the harem and flaps its sacs toward her in a behavior known as “salting.” Typically, salting is reserved for visiting females outside of the harem, whereas established females receive a hovering display and courtship song which may go on, intermittently, for one hour. A female usually responds by flying away or swatting at the male with her wing (80% of copulation attempts); or she may reciprocate with a less complex social call that is often a precursor to copulation. Harem size is positively correlated with song complexity (number of syllables in a song), as well as with frequency of male displays. Additionally, molecular studies have verified that male reproductive success is positively correlated with harem size.

A single male guards the harem from non-harem males both at the roost and when the harem forages at night. A male may use a short territorial song to ward off other males, and antagonistic encounters between males are resolved after a brief barking match. However, within a harem, cryptic males wait to usurp the harem if the harem male is removed. Based on removal studies, the succession of harem males by cryptic males depends on tenure within the colony; cryptic males that have been in a harem the longest take over the harem. This suggests a seniority-based hierarchy among males and may be one reason why males are highly philopatric, in hopes that their fidelity to the harem will eventually result in access to the females.

Researchers have also observed a social hierarchy in the females of a harem. A female that consistently wins dyadic interactions against other females tends to position herself in the warmest area of the roost, highest from the ground. These females experience fewer copulation attempts from the harem male and tend to change roosts less often than females of a lesser rank. They also try to drive off females looking to join the harem, but will relent if a new female is persistent. Harem fidelity is relatively low among females, with one study finding that 60% of females visit at least 3 harems per day. Visiting females receive a majority of the copulation attempts and harassment from harem males.

Mating System: polygynous ; polygynandrous (promiscuous)

Although males work to maintain a harem throughout the year, females are typically receptive to copulation once a year. In Costa Rica, females allow males to breed with them during an approximate four week period in December and January, which coincides with the end of the seasonal rains. During the breeding season, a male’s testes swell to 0.2% of his body mass. Fertilization and implantation occurs soon after copulation, and a fetus is recognizable eight weeks after fertilization. However, fetal development slows dramatically at this point, since gestation lasts six months.

In Costa Rica, births occur in a three week span from May to June with pregnant females in a colony undergoing synchronous parturition. This period is generally the onset of the rainy season, but in years where the rains are delayed, a stressed female is able to resorb or abort a pregnancy. Successful pregnancies result in a single newborn that is fully furred, weighs 40% of its mother’s mass, and has a forearm length that is 60% of the adult forearm length. As the offspring mature, 75% of males stay in the colony while all females leave. Of females that leave, 16% go on to inhabit a neighboring colony, whereas the outcome of the other 84% is unknown.

Breeding interval: Greater sac-winged bats breed once annually.

Breeding season: Breeding season lasts for about 4 weeks between December and January (at the conclusion of the rainy season).

Average number of offspring: 1.

Average gestation period: 6 months.

Average weaning age: 2 months.

Average time to independence: 2 months.

Average age at sexual or reproductive maturity (female): 12 months.

Range age at sexual or reproductive maturity (male): 7 (low) months.

Average age at sexual or reproductive maturity (male): 12 months.

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

Only females provide direct parental care. Although they are relatively well developed, newborns cling to their mothers until their first flight 10 to 14 days after birth. Lactation continues for another 6 weeks, at which point juveniles becomes fully independent. Adult males, despite having no direct parental investment, are important in how juveniles learn and practice vocalizations. Using bat detectors, researchers discovered that juveniles appear to mix rudimentary elements of several call types much in the same way many juvenile birds and infant humans babble incoherently when first learning to communicate (only documented case of babbling in a mammalian species outside of primates).

Parental Investment: altricial ; pre-fertilization (Provisioning, Protecting: Female); pre-hatching/birth (Provisioning: Female, Protecting: Female); pre-weaning/fledging (Provisioning: Female, Protecting: Female); inherits maternal/paternal territory

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Luzynski, K. and E. Sluzas 2009. "Saccopteryx bilineata" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Saccopteryx_bilineata.html
author
Ken Luzynski, University of Michigan-Ann Arbor
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Emily Sluzas, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Tanya Dewey, Animal Diversity Web
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Greater sac-winged bat

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The greater sac-winged bat (Saccopteryx bilineata) is a bat of the family Emballonuridae native to Central and South America.[2]

They are the most common bats seen in the rainforest, as they often roost on the outside of large trees. They are insectivores and use echolocation calls through the mouth to track their prey, which includes flies, beetles, butterflies and moths.[3][4] The long nose and upper lip are highly mobile and can shift upward to enlarge the mouth opening.

Close-up of male wing pouch
Close-up of a greater sac-winged bat

The term "sac-winged" refers to small pouches on the wings. These sacs are used by males to attract females and to mark their harem territory. During daily grooming, males will fill these sacs with drops of urine and glandular secretions. During displays for females, the male will hover in front of the female and fan her vigorously to expose her to the scent of the mixture in the wing sacs. Males will also shake the contents of the sac towards bats outside of the male's harem territory to warn off intruders.[5] Microbial fermentation in the sac may produce identifiable scent signals.[6]

Sac-wing pups have been recorded making various calls in a jumbled context. For example, a female pup will give the male trill of courting followed by echolocation clicks then adult territorial challenges. These mixed-up vocalizations have been equated with human infant babbling and mispronounced songs of young birds. This is the first example of mammal babbling outside of the primate order.[7]

References

  1. ^ Solari, S. (2015). "Saccopteryx bilineata". IUCN Red List of Threatened Species. 2015: e.T19804A22004716. doi:10.2305/IUCN.UK.2015-4.RLTS.T19804A22004716.en.
  2. ^ Simmons, N.B. (2005). "Order Chiroptera". In Wilson, D.E.; Reeder, D.M (eds.). Mammal Species of the World: A Taxonomic and Geographic Reference (3rd ed.). Johns Hopkins University Press. p. 390. ISBN 978-0-8018-8221-0. OCLC 62265494.
  3. ^ https://sta.uwi.edu/fst/lifesciences/sites/default/files/lifesciences/documents/ogatt/Saccopteryx_bilineata%20-%20Greater%20Sac-winged%20Bat.pdf
  4. ^ "Saccopteryx bilineata (Greater sac-winged bat)". Animal Diversity Web.
  5. ^ Voigt, CC; von Helversen, O (December 1999). "Storage and display of odour by male Saccopteryx bilineata (Chiroptera, Emballonuridae)". Behavioral Ecology and Sociobiology. 47 (1–2): 29–40. doi:10.1007/s002650050646. S2CID 11339644.
  6. ^ Voigt, C. C.; Caspers, B.; Speck, S. (2005). "Bats, Bacteria, and Bat Smell: Sex-Specific Diversity of Microbes in a Sexually Selected Scent Organ". Journal of Mammalogy. 86 (4): 745. doi:10.1644/1545-1542(2005)086[0745:BBABSS]2.0.CO;2. ISSN 1545-1542. pdf Archived 31 March 2012 at the Wayback Machine
  7. ^ Knornschild, M; Behr O; von Helversen O (September 2006). "Babbling behavior in the sac-winged bat (Saccopteryx bilineata)". Naturwissenschaften. 93 (9): 451–4. doi:10.1007/s00114-006-0127-9. PMID 16736178. S2CID 33556162.
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Greater sac-winged bat: Brief Summary

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The greater sac-winged bat (Saccopteryx bilineata) is a bat of the family Emballonuridae native to Central and South America.

They are the most common bats seen in the rainforest, as they often roost on the outside of large trees. They are insectivores and use echolocation calls through the mouth to track their prey, which includes flies, beetles, butterflies and moths. The long nose and upper lip are highly mobile and can shift upward to enlarge the mouth opening.

Close-up of male wing pouch Close-up of a greater sac-winged bat

The term "sac-winged" refers to small pouches on the wings. These sacs are used by males to attract females and to mark their harem territory. During daily grooming, males will fill these sacs with drops of urine and glandular secretions. During displays for females, the male will hover in front of the female and fan her vigorously to expose her to the scent of the mixture in the wing sacs. Males will also shake the contents of the sac towards bats outside of the male's harem territory to warn off intruders. Microbial fermentation in the sac may produce identifiable scent signals.

Sac-wing pups have been recorded making various calls in a jumbled context. For example, a female pup will give the male trill of courting followed by echolocation clicks then adult territorial challenges. These mixed-up vocalizations have been equated with human infant babbling and mispronounced songs of young birds. This is the first example of mammal babbling outside of the primate order.

Saccopteryx bilineata scenting display call (slow-mo) Recorded at the Tiputini Biodiversity Station Problems playing this file? See media help.
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