Bats are the only mammal capable of true flight. Bats use flight for capturing prey, breeding, avoiding predators, and long-distance migration. Bat wing morphology is often highly specialized to the needs of the species.
Charles Darwin foresaw an issue with his theory of evolution by natural selection in the evolution of complex traits such as eyes or "the structure and habits of a bat." Indeed, the oldest bat fossils are very similar in wing morphology to the bats of today, despite living and dying 52.5 million years ago. The common ancestor of all bats is hypothesized to have been an arboreal quadruped of the northern hemisphere. This ancestor is predicted to have lived 64 million years ago at the border of the Cretaceous and Paleogene, based on molecular and paleontological data. There is a gap in the fossil record, and no transitional fossils exist from this quadrupedal ancestor to the appearance of the modern bat. It is unclear how long the transition from quadrupedalism to powered flight took. After evolving powered flight, bats underwent massive adaptive radiation, becoming the second-most speciose mammal order, after rodents.
Recent studies have shown that, rather than having evolved from gliders, the ancestors of bats were flutterers.
Adaptations for flight
To make powered flight possible, bats had to evolve several features. Bat flight necessitated the increase of membrane surface area between the digits of the forelimbs, between the forelimbs and hindlimbs, and between the hindlimbs. Bats also had to evolve a thinner cortical bone to reduce torsional stresses produced by propulsive downstroke movements. Bats had to reroute innervation to their wing muscles to allow for control of powered flight. The strength and mass of forelimb musculature also had to be increased to allow powerful upstrokes and downstrokes.
The chord length of a bat wing is the distance from the leading edge to the trailing edge measured parallel to the direction of flight. The mean chord length is a standardized measure which captures a representative chord length over a whole flap cycle. Given wing area S, and wingspan b, the mean chord can be calculated by,
Aspect ratio has been calculated with different definitions. The two methods outlined here give different, non-comparable values. The first method of calculation uses the wingspan b, and the wing area S, and is given by,
Using this definition, typical values of aspect ratio fall between 5 and 11 depending on the wing morphology of a given species. Faster flight speed is significantly correlated with higher aspect ratios. Higher aspect ratios decrease the energetic costs of flight, which is beneficial to migratory species.
Another way to calculate the wing aspect ratio is by taking the length of the wrist to the tip of the third finger, adding the length of the forearm, and then dividing that total by the distance from the wrist to the fifth finger.
In a meta analysis covering 257 species of bats, higher relative wing loading values were observed in bats which fly at higher velocities, while lower wing loading values were correlated with improved flight maneuverability. Additionally, bats with lower wing loading were seen to have better mass-carrying ability, and were able carry larger prey while flying.
Wing morphology as it relates to ecology
Bats that consume insects by hawking (aerial pursuit and capture) must be able to travel at fast speeds, and must employ a high level of maneuverability. Morphological adaptations that favor this style of flight include high wing loading, long and pointed wingtips, and wings with high aspect ratios. The bat family Molossidae is considered highly specialized at hawking, with unusually high aspect ratios and wing loading. These traits make them capable of incredibly-fast speeds. Mexican free-tailed bats are thought to be the fastest animal on earth, capable of horizontal flight speeds over a level surface up to 160 km/hr (99 mph).
Bats that glean insects capture stationary prey on a solid substrate. This foraging method requires bats to hover above the substrate and listen for insect noises. Short, rounded wingtips in gleaning bats may be advantageous to allow maneuverability of flight in cluttered airspace. Pointed wingtips may be detrimental to a bat's ability to glean insects.
Bats with this foraging style pluck insects off the surface of a body of water. Piscivores employ the same flight style to catch fish just below the water's surface. Trawling bats travel at slower speeds, which means that they require low wing loading.
Frugivores have below-average aspect ratios. Fruit-eating bats have variable wing-loading, which corresponds to vertical stratification of rain forests. Fruit-eating bats that travel below the canopy have higher wing-loading; bats that travel above the canopy have intermediate wing-loading; bats that travel in the understory have low wing-loading. This pattern of decreasing wing-loading as airspace becomes more cluttered is consistent with data that suggest that lower wing-loading is associated with greater maneuverability.
Nectarivores, like gleaners, will frequently employ hovering during foraging. Hovering nectarivores are more likely to have rounded wingtips, which aids in maneuverability. Nectarivores that land on the flower before feeding have worse maneuverability. Nectarivores in general have lower aspect ratios, which makes them more suited to flight in a cluttered environment. Nectarivores that migrate to seasonal food resources, such as the genus Leptonycteris, have lower wing-loading than nectarivorous species with small home ranges.
Bats that consume non-insect animal prey are benefited by low wing-loading, which allows them to lift and carry larger prey items. This increased capacity for lift even allows them to take flight from the ground while carrying a prey item that is half of their body weight.
The three species of sanguinivorous bats belong to the subfamily Desmodontinae. These bats are characterized by relatively high wing-loading and short or average wingspans. The high wing-loading allows them faster flight speeds, which is advantageous when they have to commute long distances from their roosts to find prey. The common vampire bat has an average aspect ratio and very short, slightly rounded wingtips. The hairy-legged vampire bat has the lowest aspect ratio of the three species; it also has relatively long and rounded wingtips. Hairy-legged vampire bats are more adapted to maneuverable flights than the other two species. The white-winged vampire bat has the highest aspect ratio of the three species, which means it is most adapted to long flights.
- Darwin, C. (1968). On the origin of species by means of natural selection. 1859. London: Murray Google Scholar.
- Sears, K. E., Behringer, R. R., Rasweiler, J. J., & Niswander, L. A. (2006). Development of bat flight: morphologic and molecular evolution of bat wing digits. Proceedings of the National Academy of Sciences, 103(17), 6581-6586.
- Teeling, E. C., Springer, M. S., Madsen, O., Bates, P., O'brien, S. J., & Murphy, W. J. (2005). A molecular phylogeny for bats illuminates biogeography and the fossil record. Science, 307(5709), 580-584.
- Cooper, K. L., & Tabin, C. J. (2008). Understanding of bat wing evolution takes flight. Genes & development, 22(2), 121-124.
- Nowak, R. M. (1994). Walker's bats of the world. JHU Press.
- Kaplan, Matt (2011). "Ancient bats got in a flap over food". Nature. doi:10.1038/nature.2011.9304.
- Swartz, S. M., Bennett, M. B., & Carrier, D. R. (1992). Wing bone stresses in free flying bats and the evolution of skeletal design for flight. Nature, 359(6397), 726.
- Thewissen, J. G. M., & Babcock, S. K. (1991). Distinctive cranial and cervical innervation of wing muscles: new evidence for bat monophyly. Science, 251(4996), 934-937.
- Thewissen, J. G. M., & Babcock, S. K. (1992). The origin of flight in bats. BioScience, 42(5), 340-345.
- J., Pennycuick, Colin (1989). Bird flight performance : a practical calculation manual. Oxford University Press. ISBN 0198577214. OCLC 468014494.
- Von Busse, R.; Hedenstrom, A.; Winter, Y.; Johansson, L. C. (2012-10-11). "Kinematics and wing shape across flight speed in the bat, Leptonycteris yerbabuenae". Biology Open. 1 (12): 1226–1238. doi:10.1242/bio.20122964. ISSN 2046-6390.
- Farney, J., & Fleharty, E. D. (1969). Aspect ratio, loading, wing span, and membrane areas of bats. Journal of Mammalogy, 50(2), 362-367.
- Norberg and Rayner (1987). Ecological morphology and flight in bats (Mammalia; Chiroptera): wing adaptations, flight performance, foraging strategy and echolocation. Philosophical Transactions of the Royal Society of London B: Biological Sciences 316.1179 (1987): 335–42.
- Hedenström, A.; Johansson, L. C.; Wolf, M.; Busse, R. von; Winter, Y.; Spedding, G. R. (2007-05-11). "Bat Flight Generates Complex Aerodynamic Tracks". Science. 316 (5826): 894–897. doi:10.1126/science.1142281. ISSN 0036-8075. PMID 17495171.
- "Recent progress in flapping wing aerodynamics and aeroelasticity". Progress in Aerospace Sciences. 46 (7): 284–327. 2010-10-01. doi:10.1016/j.paerosci.2010.01.001. ISSN 0376-0421.
- Findley, J. S., Studier, E. H., & Wilson, D. E. (1972). Morphologic properties of bat wings. Journal of Mammalogy, 53(3), 429-444.
- Freeman, P. W. (1981). A multivariate study of the family Molossidae (Mammalia, Chiroptera): morphology, ecology, evolution. Mammalogy papers: University of Nebraska State Museum, 26.
- McCracken, G. F., Safi, K., Kunz, T. H., Dechmann, D. K., Swartz, S. M., & Wikelski, M. (2016). Airplane tracking documents the fastest flight speeds recorded for bats. Royal Society Open Science, 3(11), 160398.
- Schmidt, S., Hanke, S., & Pillat, J. (2000). The role of echolocation in the hunting of terrestrial prey–new evidence for an underestimated strategy in the gleaning bat, Megaderma lyra. Journal of Comparative Physiology A, 186(10), 975-988.
- Stoffberg, S., & Jacobs, D. S. (2004). The influence of wing morphology and echolocation on the gleaning ability of the insectivorous bat Myotis tricolor. Canadian journal of zoology, 82(12), 1854-1863.
- Hodgkison, R., Balding, S. T., Zubaid, A., & Kunz, T. H. (2004). Habitat structure, wing morphology, and the vertical stratification of Malaysian fruit bats (Megachiroptera: Pteropodidae). Journal of Tropical Ecology, 20(06), 667-673.