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Home -> Kingdom Animalia -> Phylum Chordata -> Subphylum Vertebrata -> Class Mammalia -> Order Chiroptera -> Family Phyllostomidae -> Subfamily Stenodermatinae -> Species Sturnira lilium

Sturnira lilium
little yellow-shouldered bat



2009/11/22 05:05:02.898 US/Eastern

By Alexandra Anderson

Kingdom: Animalia
Phylum: Chordata
Subphylum: Vertebrata
Class: Mammalia
Order: Chiroptera
Family: Phyllostomidae
Subfamily: Stenodermatinae
Genus: Sturnira
Species: Sturnira lilium

Geographic Range

Little yellow-shouldered bats are found in the neotropics, ranging from North Mexico (including Sonora and Tamaulipas) through Central America and tropical and subtropical South America to Chile. This includes northern Argentina, eastern and southern Brazil, and the Lesser Antilles. (Gannon et al., 1989; Mello, Kalko, and Silva, 2008; Stoner, 2001; Vieira and Carvalho-Okano, 1994; Wilson and Reeder, 2005)

Biogeographic Regions:
neotropical (native ); oceanic islands (native ).

Habitat

Elevation
1000 m (high)
(3280 ft)


Little yellow-shouldered bats occupy many different types of forest habitats, including mountainous forests (Mello, Kalko, and Silva, 2008), semi-deciduous tropical rainforests, and humid and semi-arid forests. They are also found in tropical lowlands and open areas, such as fields or farmland. They are common near streams or other bodies of water. They are not found at elevations over 1,000 m (Gannon et al., 1989). Little yellow-shouldered bats commonly roost in tree cavities in lower canopy levels, especially in mature trees with diameters 50% larger than surrounding trees. They prefer to roost in the tree species: Pimenta dioica, Metopium brownei, Vitex gaumeri, and Pseudobombax ellipticum, most likely because the heartwood of these trees easily decays, resulting in hollows (Evelyn and Stiles, 2003). They also roost in manmade structures and caves (Gannon et al., 1989). (Evelyn and Stiles, 2003; Gannon et al., 1989; Mello, Kalko, and Silva, 2008)

These animals are found in the following types of habitat:
tropical ; terrestrial .

Terrestrial Biomes:
forest ; rainforest .

Other:
agricultural ; riparian ; caves.

Physical Description

Mass
13 to 18 g
(0.46 to 0.63 oz)


Length
62 to 65 mm
(2.44 to 2.56 in)


Wingspan
30 cm (average)
(11.81 in)


Little yellow-shouldered bats are medium-sized bats with total lengths of 62 to 65 mm, forearm lengths of 36.6 to 45.0 mm, and average wingspan of 30 cm (Vieira and Carvalho-Okano, 1994). Males tend to have slightly larger total length and cranial measurements than females (Gannon et al., 1989). Typical mass is 13 to 18g (Evelyn and Stiles, 2003). They have short, broad ears with a tragus that is one-third the size of the ear. They also have distinct nose leaves. No tail is present and calcars are extremely small or absent. Coloring varies by gender, age, and geography. Dorsal fur can be dark gray to reddish-brown and the ventral fur is always lighter than the dorsal fur. The head, neck, and shoulder hairs have a yellow tint due to yellow hair shafts and with dark-brown tips. Males tend to have yellow to red stained shoulder hairs that look like straps on a soldier’s uniform due to an excretion from their shoulder glands. It is this coloring that gives S. lilium the common name "little yellow-shouldered bat." The patagia is solid brown (Gannon et al., 1989). (Evelyn and Stiles, 2003; Gannon et al., 1989; Nowak, 1991; Vieira and Carvalho-Okano, 1994)

Little yellow-shouldered bats are homoiothermic, with an average body temperature of 36.4 degrees Celsius and a range from 34 to 38 degrees Celsius. They have been known to survive with a body temperature of 41 degrees Celsius (Gannon et al., 1989). (Gannon et al., 1989)

Some key physical features:
endothermic ; homoiothermic; bilateral symmetry .

Sexual dimorphism: male larger, sexes colored or patterned differently.

Reproduction

Breeding interval
Little yellow-shouldered bats breed twice yearly.

Breeding season
Little yellow-shouldered bat reproduction seems to peak at 3 times during the year, although reproduction may occur year-round.

Number of offspring
1 (average)

Gestation period
4 to 7 months

Time to weaning
5 to 20 weeks

Time to independence
1 months (average)

Age at sexual or reproductive maturity (female)
8 to 11 months

Age at sexual or reproductive maturity (male)
8 to 11 months

The mating systems of Sturnira lilium have not been extensively studied. Other phyllostomids do not tend to be promiscuous (Wilkinson and McCracken, 2006). Little yellow-shouldered bats tend to roost individually and the ratio of male testes size to body mass is relatively low, suggesting that sperm competition is not very high between males. Both of these factors decrease the likelihood of promiscuity in S. lilium, but the possibility cannot be ruled out. More research on the mating systems of S. lilium is needed. Reproduction of males corresponds with receptivity in females (Fleming, Hooper, and Wilson, 1972) and adult males secrete a strong scent from their shoulder glands attract a mate. This scent is what gives their fur the yellow coloration on their shoulders (Gannon et al., 1989). (Fleming, Hooper, and Wilson, 1972; Gannon et al., 1989; Grzimek, 1990; Wilkinson and McCracken, 2006)

Little yellow-shouldered bats exhibit seasonal, bimodal polyestry (Fleming, Hooper, and Wilson, 1972), reproducing twice a year, once in the dry season and once in the rainy season. There is also a pattern of bimodal peaks in pregnancy and lactation in females bats, but pregnancy has been recorded in every month of the year (Nowak, 1991). Reproductive activity peaks in three periods throughout the year, generally February to June, October, and December (Fleming, Hooper, and Wilson, 1972). The exact length of gestation is unknown, gestation length in other phyllostomids is from four to seven months (Grzimek, 1990). Females give birth to one pup, but births occur twice a year, once towards the end of the dry season and once in the middle-to-late rainy season (Stoner, 2001). Biologists debate whether this seasonal birthing pattern is triggered by food availability or temperature cues (Mello, Kalko, and Silva, 2008). Information birth mass is unavailablebut, phyllostomids have the largest young to maternal mass ratio of any other bat family, with young weighing up to 14% of adult weight at birth (Grzimek, 1990). This larger birth mass is most likely the result of a longer gestation period, allowing for faster post-natal growth of young. Young phyllostomids are born with well developed hind limbs, open eyes, and fur when born. It takes from 5 to 20 weeks to wean young (Kurta and Kunz, 1987). Young phyllostomids tend to become independent 1 month after birth. Juveniles reach sexual or reproductive maturity at 8 to 11 months of age (Fleming, Hooper, and Wilson, 1972). (Fleming, Hooper, and Wilson, 1972; Gannon et al., 1989; Grzimek, 1990; Kurta and Kunz, 1987; Mello, Kalko, and Silva, 2008; Nowak, 1991; Stoner, 2001)

Key reproductive features:
iteroparous ; seasonal breeding ; year-round breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; viviparous .

It is unclear whether females use maternity colonies to raise young. Though the young are well developed when born, they must be nursed by their mother for several weeks after birth. Male parental investment has not been documented. Frugivorous bats are more likely than carnivorous or insectivorous bats to carry young while foraging, so it is possible that females carry their young when looking for food (Jones, 2000). (Jones, 2000)

Parental investment:
precocial ; pre-fertilization (provisioning, protecting: female); pre-hatching/birth (provisioning: female, protecting: female); pre-weaning/fledging (provisioning: female, protecting: female).

Lifespan/Longevity

Average lifespan (wild)
20 years

Little yellow-shouldered bats live for approximately 20 years in the wild. (Grzimek, 1990)

Behavior

Little yellow-shouldered bats often roost alone, but they can roost in groups as large as 10. It is unclear whether males and females roost together or separately (Evelyn and Stiles, 2003). Little yellow-shouldered bats are nocturnal and relatively inactive during daylight hours. At night they fly through the forest understory, canopy, and open areas. They can fly quickly in open areas but can also maneuver well in dense forests (Jennings et al., 2004). Individuals in high altitudes may migrate to warmer areas during colder months due to a lack of fat reserves and an inability to sustain long periods of torpor (Mello, Kalko, and Silva, 2008). (Evelyn and Stiles, 2003; Jennings et al., 2004; Mello, Kalko, and Silva, 2008)

Home Range

Compared to other South American bats, little yellow-shouldered bats tend to have relatively small ranges. Banding studies show that they roost and forage in the same area for several years at a time (Fleming, Hooper, and Wilson, 1972). (Fleming, Hooper, and Wilson, 1972)

Key behaviors:
troglophilic; flies; nocturnal ; motile ; migratory ; sedentary ; daily torpor; solitary ; social .

Communication and Perception

Little yellow-shouldered bats use echolocation to navigate. Because they are frugivorous, their echolocation is not as specialized as bats that feed on insects. They use echolocation frequencies with low duty frequency and four harmonics. Low duty frequencies are excellent for short-range detection (Jennings et al., 2004). Little yellow-shouldered bats, like other bats, use vocalizations in frequencies audible to humans to communicate as well. The reduced horseshoe and spear structures on the noseleaf may suggest that these bats use olfaction to find food (Arita, 1990). Although nocturnal, little yellow-shouldered bats use visual information to evaluate their surroundings. Phyllostomids, including little yellow-shouldered bats, have larger visual centers in their brain compared to other bats, suggesting that vision plays a more significant role in their lives. Their night vision exceeds that of humans, which is a benefit when foraging. The yellow shoulder color of males also suggests that vision is important in sexual selection (Altringham and Fenton, 2006). The spicy smelling pheromones secreted from the shoulders of males are also important forms of chemical communication between potential mates (Gannon et al., 1989; Altringham and Fenton, 2006). (Altringham and Fenton, 2006; Arita, 1990; Gannon et al., 1989; Jennings et al., 2004)

Communicates with:
visual ; acoustic ; chemical .

Other communication keywords:
pheromones .

Perception channels:
visual ; tactile ; acoustic ; ultrasound ; echolocation ; chemical .

Food Habits

Little yellow-shouldered bats are frugivorous. They prefer to eat fruits of plants in the Solanaceae family (nightshade family). When they are unavailable or low in abundance, these bats supplement their diet with fruits of the Piperaceae (pepper) and Cecropiaceae (nettles or cecropias) families (Mello, Kalko, and Silva, 2008). They occasionally drink nectar. Little yellow-shouldered bats begins foraging at dusk and tend to forage in the forest understory (Evelyn and Stiles, 2003). They search for food in shrubs and low trees but also forage at canopy level. They handle understory fruit quickly and canopy fruit slowly. Little yellow-shouldered bats can consume several fruits in a 5 to 15 minute time period. After eating, they pause to digest food, usually excreting within 20 minutes of consumption. They forage for up to 4 hours nightly (Bonaccorso, 1987). (Bonaccorso, 1987; Evelyn and Stiles, 2003; Mello, Kalko, and Silva, 2008)

Primary Diet:
herbivore (frugivore ).

Plant Foods:
fruit; nectar.

Predation

Known predators

Known predators of S. lilium include humans, snakes, opossums, raptors, monkeys, and spectral bats (Evelyn and Stiles, 2003). Many of these predators are avoided by night foraging. Their dark color helps conceal them during foraging periods and flight is an advantage in escaping non-volant predators. (Evelyn and Stiles, 2003)

Anti-predator adaptations::
cryptic .

Ecosystem Roles

Little yellow-shouldered bats are important in the dispersal of seeds of tropical plants, especially those of the Solanaceae family (Mello, Kalko, and Silva, 2008). They are the primary dispersers of seeds of Solanum riparium (Iudica and Bonaccorso, 1997). They are also important pollinators of Mabea fistulifera and other flowering plants (Vieira and Carvalho-Okano, 1994). Their seed dispersal and pollination roles make them important in the regeneration of forests. (Iudica and Bonaccorso, 1997; Mello, Kalko, and Silva, 2008; Vieira and Carvalho-Okano, 1994)

Many parasite species use little yellow-shouldered bats as hosts. Endoparasites, such as nematodes, and ectoparasites, such as mites, bat flies, and ticks are all found on this species (Gannon et al., 1989). (Gannon et al., 1989)

Key ways these animals impact their ecosystem:
disperses seeds; pollinates; creates habitat.

Species (or larger taxonomic groups) that are mutualists with this species
  • Solanum riparium
  • Mabea fistulifera
Commensal or parasitic species (or larger taxonomic groups) that use this species as a host
  • nematodes (Capillaria pusilla)
  • nematodes (Filaria serpiculum)
  • nematodes (Litomosoides caliensis)
  • mites (Cameronieta elongatus)
  • mites (Chirnyssoides brasiliensis)
  • mites (Chiroptonyssus haematophagus)
  • mites (Eudusbabekia lepidoseta)
  • mites (Eutrombicula goeldii)
  • mites (Hooperella vesperuginis)
  • mites (Loomisia desmodus)
  • mites (Macronyssus)
  • mites (Microtrombiula sturnirae)
  • mites (Parakosa tadarida)
  • mites (Paralabidocarpus artibei)
  • mites (Parichoronyssus euthysternum)
  • mites (Periglischrus acutisternus)
  • mites (Periglischrus caligus)
  • mites (Periglischrus herrerai)
  • mites (Periglischrus iheringi)
  • mites (Periglischrus ojastii)
  • mites (Periglischrus vargasi)
  • mites (Radfordiella)
  • mites (Trichobioides perspicillatus)
  • bat flies (Aspodoptera delatorrei)
  • bat flies (Aspodoptera falcate)
  • bat flies (Aspodoptera phyllostomatis)
  • bat flies (Exastinion clovisi)
  • bat flies (Megistopoda proxima)
  • ticks (Ornithodoros hasei)
  • ticks (Nycteriglyphus sturnirae)
  • ticks (Ixodes)

Economic Importance for Humans: Negative

Little yellow-shouldered bats have few negative impacts on humans. The most notable would be their potential to carry disease and viruses such as rabies, but interactions with humans are rare. (Grzimek, 1990)

Ways that these animals might be a problem for humans:
injures humans (causes disease in humans ); causes or carries domestic animal disease .

Economic Importance for Humans: Positive

In addition to helping regenerate economically valuable forest habitats, little yellow-shouldered bats and other frugivorous bats have positive impacts on farming and agriculture. They help in the pollination of crops and shade and support trees. Citrus, cocoa, coffee, allspice, mixed vegetation, and live fence vegetation have all been reported to benefit from these bats. Despite their appetite for fruit, farmers report that frugivorous bats such as S. lilium are not destructive to their main crops (Estrada, Coates-Estrada, and Meritt, 1993). (Estrada, Coates-Estrada, and Meritt, 1993)

Ways that people benefit from these animals:
food ; pollinates crops.

Conservation Status

IUCN Red List: [link]:
Not Evaluated.

US Federal List: [link]:
No special status.

CITES: [link]:
No special status.

State of Michigan List: [link]:
No special status.

Little yellow-shouldered bats tolerate and adapt to deforestation well compared to other species. They are the most abundant bat species in disturbed forest areas. Deforestation is a concern, however, because of their preference for roosting in large diameter, mature trees that are often harvested first (Evelyn and Stiles, 2003). Neither the IUCN Red List, US Federal List, or CITES suggest S. lilium is a species to be concerned about at this time. (Evelyn and Stiles, 2003; International Union for Conservation of Nature and Natural Resources (IUCN), 2009)

Contributors

Alexandra Anderson (author), University of Wisconsin Stevens Point. Chris Yahnke (editor, instructor), University of Wisconsin Stevens Point.
Tanya Dewey (editor), Animal Diversity Web, University of Michigan Museum of Zoology.

References

Altringham, J., M. Fenton. 2006. Sensory Ecology and Communication in the Chiroptera. Pp. 90-127 in T. Kunz, M. Fenton, eds. Bat Ecology. Chicago, IL: University of Chicago Press. Accessed August 09, 2009 at http://books.google.com/books?hl=en&lr=&id=kqp02jzUzwgC&oi=fnd&pg=PA90&dq=Sturnira+lilium+%22offspring%22&ots=252sd3jVec&sig=gTwI9PCY1FOmaP-8RQ00tQEmyw8#v=onepage&q=&f=false.

Arita, H. 1990. Noseleaf Morphology and Ecological Correlates in Phyllostomid Bats. Journal of Mammalogy, Vol. 71, No. 1: 36-47. Accessed August 02, 2009 at http://www.jstor.org.ezproxy.uwsp.edu/stable/1381314?seq=8.

Bonaccorso, F. 1987. Feeding Behavior and Foraging Strategies of Captive Phyllostomid Fruit Bat an Experimental Study. Journal of Animal Ecology, Vol. 56, No. 3: 907-920. Accessed July 26, 2009 at http://www.jstor.org.ezproxy.uwsp.edu/stable/4956?seq=4.

Estrada, A., R. Coates-Estrada, D. Meritt. 1993. Bat species richness and abundance in tropical rain forest fragments and in agricultural habitats at Los Tuxtlas, Mexico. ECOGRAPHY, Vol. 16, Ed. 4: 309-318. Accessed August 05, 2009 at http://web.ebscohost.com.ezproxy.uwsp.edu/ehost/pdf?vid=2&hid=2&sid=a24b5d22-00de-4531-94d8-f0f3885d184d%40sessionmgr4.

Evelyn, M., D. Stiles. 2003. Roosting Requirements of Two Frugivorous Bats (Sturnira lilium and Arbiteus intermedius) in Fragmented Neotropical Forest. BIOTROPICA, Vol. 35, no. 3: 405-418. Accessed July 26, 2009 at http://www.bioone.org.ezproxy.uwsp.edu/doi/full/10.1646/02063.

Fleming, T., E. Hooper, D. Wilson. 1972. Three Central American Bat Communities: Structure, Reproductive Cycles, and Movement Patterns. Ecology, Vol. 53, No. 4: 555-569. Accessed July 28, 2009 at http://www.jstor.org.ezproxy.uwsp.edu/stable/1934771.

Gannon, M., M. Willig, J. Jones, Jr.. 1989. Sturnira lilium. The American Society of Mammalogists, No. 333: 1-5. Accessed July 27, 2009 at http://www.jstor.org.ezproxy.uwsp.edu/stable/3504237.

Grzimek, B. 1990. Bats. Pp. 584-611 in B. Grzimek, ed. Grzimek's Encyclopedia of Mammals, Vol. 1, 2 Edition. New York, NY: Mcgraw-Hill Publishing Co..

International Union for Conservation of Nature and Natural Resources (IUCN). 2009. "IUCN Red List of Threatened Species" (On-line). Accessed July 26, 2009 at http://www.iucnredlist.org/search.

Iudica, C., F. Bonaccorso. 1997. Feeding of the Bat, Sturnira lilium, on Fruits of Solanum Riparium Influences Dispersal of This Pioneer Tree In Forests of Northwestern Argentina. Studies on Neotropical Fauna & Environment, Vol. 32 Issue 1: 4. Accessed July 26, 2009 at http://web.ebscohost.com.ezproxy.uwsp.edu/ehost/pdf?vid=2&hid=107&sid=e6901035-c2ab-46b2-9b63-17720d14efab%40sessionmgr111.

Jennings, N., S. Parsons, K. Barlow, M. Gannon. 2004. Echolocation calls and wing morphology of bats from the West Indies. Acta Chiropterologica, Vol. 6, 1: 75–90. Accessed August 02, 2009 at http://www.personal.psu.edu/mrg5/WIecholocation.pdf.

Jones, G. 2000. Ontogeny, Evolution and Phylogeny of Social Behavior. Pp. 362-384 in R. Adams, S. Pederson, eds. Ontogeny, Functional Ecology, and Evolution of Bats. New York, NY: Cambridge University Press.

Kurta, A., T. Kunz. 1987. Size of Bats at Birth and Maternal Investment During Pregnancy. Symposia of the Zoological Society of London, No. 57: 79-106. Accessed August 02, 2009 at http://www.bu.edu/cecb/BATS/reprints/1987/Symp.Zool(57)%3B79-106%20(1987).pdf.

Mello, M., E. Kalko, W. Silva. 2008. Diet and Abundance of the Bat Sturnira lilium (Chiroptera) in a Brazilian Montane Atlantic Forest. Journal of Mammalogy, Vol. 89 Issue 2: 485-492. Accessed July 26, 2009 at http://www.bioone.org.ezproxy.uwsp.edu/doi/full/10.1644/06-MAMM-A-411R.1.

Nowak, R. 1991. Yellow-shouldered Bats, or American Epauleted Bats. Pp. 299-300 in Walker's Mammals of the World, Vol. 1, 5 Edition. Baltimore, MD: Johns Hopkins University Press.

Stoner, K. 2001. Differential habitat use and reproductive patterns of frugivorous bats in tropical dry forest of northwestern Costa Rica. Canadian Journal of Zoology, Vol. 79 Issue 9: p1626. Accessed July 26, 2009 at http://web.ebscohost.com.ezproxy.uwsp.edu/ehost/pdf?vid=2&hid=107&sid=696e5103-e32d-4b1b-a37c-dcf4ef2b4125%40sessionmgr104.

Valiente-Banuet, A., A. Rojas-Martínez, A. Casas, M. Coro Arizmendi, P. Dávila. 1997. Pollination biology of two winter-blooming giant columnar cacti in the Tehuacán Valley, central Mexico. Journal of Arid Environments, Volume 37, Issue 2: Pages 331-341.

Vieira, M., R. Carvalho-Okano. 1994. Pollination biology of Mabea fistulifera (Euphorbiaceae) in southeastern Brazil. Biotropica, Vol. 1 Issue 1: p73-80. Accessed July 26, 2009 at http://www.jstor.org.ezproxy.uwsp.edu/stable/2388771?seq=1.

Wilkinson, G., G. McCracken. 2006. Bats and Balls: Sexual Selection and Sperm Competition in the Chiroptera. Pp. 128-155 in T. Kunz, M. Fenton, eds. Bat Ecology. Chicago, IL: University of Chicago Press. Accessed August 02, 2009 at http://books.google.com/books?hl=en&lr=&id=kqp02jzUzwgC&oi=fnd&pg=PA128&dq=bats+and+balls&ots=252s70oWhe&sig=oZQ8GWuhLyVjozkb9gU6qwXUuF4#v=onepage&q=&f=false.

Wilson, D., D. Reeder. 2005. "Wilson & Reeder's Mammal Species of the World Third Edition" (On-line). Accessed July 26, 2009 at http://www.bucknell.edu/msw3/browse.asp?s=y&id=13801316.

2009/11/22 05:05:07.064 US/Eastern

To cite this page: Anderson, A. and C. Yahnke. 2009. "Sturnira lilium" (On-line), Animal Diversity Web. Accessed November 27, 2009 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Sturnira_lilium.html.

Disclaimer: The Animal Diversity Web is an educational resource written largely by and for college students. ADW doesn't cover all species in the world, nor does it include all the latest scientific information about organisms we describe. Though we edit our accounts for accuracy, we cannot guarantee all information in those accounts. While ADW staff and contributors provide references to books and websites that we believe are reputable, we cannot necessarily endorse the contents of references beyond our control.

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