|Townsend's big-eared bat, Corynorhinus townsendii|
The microbats constitute the now outdated suborder Microchiroptera within the order Chiroptera (bats). Bats were once differentiated into Megachiroptera and Microchiroptera, based on their size; but available molecular evidence has now shown this to be incorrect, the horseshoe bats being included in Yinpterochiroptera with the fruit bats and others. Most species which were termed Microchiroptera are now referred to as the Yangochiroptera.
The distinctions between microbats and megabats are:
- Microbats use echolocation, whereas megabats do not typically. (The Egyptian fruit bat Rousettus egyptiacus is an exception, but does not use the larynx echolocation method of microbats, instead giving scientists the theory that it clicks using its nasal passages and back of its tongue.)
- Microbats lack the claw at the second finger of the forelimb. This finger appears thinner and almost bonded by tissue with the third finger for extra support during flight.
- Megabats always lack a tail, whereas this trait only occurs in certain species of microbats.
- The ears of microbats possess a tragus (thought to be crucial in echolocation) and are respectively larger than megabat ears, whereas megabat ears are comparatively small and lack a tragus.
- Megabat eyes are quite large, whereas microbat eyes are comparatively smaller.
Microbats are 4 to 16 cm long.
The term "leaf-nose" does not indicate the diet preferred by particular species and is applied to a wide variety of microbats. Most leaf-nosed microbat species are fruit and nectar-eating. However, three species follow the bloom of columnar cacti in northwest Mexico and the Southwest United States northward in the northern spring and then the blooming agaves southward in the northern fall (autumn). Other leaf-nosed bats, such as Vampyrum spectrum of South America, hunt a variety of prey such as lizards and birds. The horseshoe bats of Europe and California leaf-nosed bat have an incredibly intricate leaf-nose for echolocation and feed primarily on insects.
Echolocation is the process where an animal produces a sound of certain wavelength, and then listens to and compares the reflected echoes to the original sound emitted. Bats use echolocation to form images of their surrounding environment and the organisms that inhabit it by eliciting ultrasonic waves via their larynx. The difference between the ultrasonic waves produced by the bat and what the bat hears provides the bat with information about its environment. Echolocation aids the bat in not only detecting prey, but also in orientation during flight.
Production of ultrasonic waves
Most microbats generate ultrasound with their larynx and emit the sound through their nose or mouth. Sound productions are generated from the vocal folds in mammals due to the elastic membranes that compose these folds. Vocalization[disambiguation needed] requires these elastic membranes because they act as a source to transform airflow into acoustic pressure waves. Energy is supplied to the elastic membranes from the lungs, and results in the production of sound. The larynx houses the vocal cords and forms the passage way for the expiratory air that will produce sound. Microbat calls (help·info) range in frequency from 14,000 to over 100,000 hertz, well beyond the range of the human ear (typical human hearing range is considered to be from 20 to 20,000 Hz). The emitted vocalizations form a broad beam of sound used to probe the environment, as well as communicate with other bats.
Laryngeally echolocating microbats
Laryngeal echolocation is the dominant form of echolocation in microbats, however, it is not the only way in which microbats can produce ultrasonic waves. Excluding non-echolocating and laryngeally echolocating microbats, other species of microbats and megabats have been shown to produce ultrasonic waves by clapping their wings, clicking their tongues, or using their nose. Laryngeally echolocating bats, in general, produce ultrasonic waves with their larynx that is specialized to produce sounds of short wavelength. The larynx is located at the cranial end of the trachea and is surrounded by cricothyroid muscles and thyroid cartilage. For reference, in humans, this is the area where the Adam's apple is located. Phonation of ultrasonic waves is produced through the vibrations of the vocal membranes in the expiratory air. The intensity that these vocal folds vibrate at varies with activity and between bat species. A characteristic of laryngeally echolocating microbats that distinguishes them from other echolocating microbats is the articulation of their stylohyal bone with their tympanic bone. The stylohyal bones are part of the hyoid apparatus that help support the throat and larynx. The tympanic bone forms the floor of the middle ear. In addition to the connection between the stylohyal bone and the tympanic bone as being an indicator of laryngeally echolocating microbats, another definitive marker is the presence of a flattened and expanded stylohyal bone at the cranial end. Microbats that laryngeally echolocate must be able to distinguish between the differences of the pulse that they produce and the returning echo that follows by being able to process and understand the ultrasonic waves at a neuronal level, in order to accurately obtain information about their surrounding environment and orientation in it. The connection between the stylohyal bone and the tympanic bone enables the bat to neurally register the outgoing and incoming ultrasonic waves produced by the larynx. Furthermore, the stylohyal bones connect the larynx to the tympanic bones via a cartilaginous or fibrous connection (depending on the species of bat). Mechanically the importance of this connection is that it supports the larynx by anchoring it to the surrounding cricothryroid muscles, as well as draws it closer to the nasal cavity during phonation. The stylohyal bones are often reduced in many other mammals, however, they are more prominent in laryngeally echolocating bats and are part of the mammalian hyoid apparatus. The hyoid apparatus functions in breathing, swallowing, and phonation in microbats as well as other mammals. An important feature of the bony connection in laryngeally echolocating microbats is the extended articulation of the ventral portion of the tympanic bones and the proximal end of the stylohyal bone that bends around it to make this connection.
The human vocalization system has been extensively studied, and as a result, is the most well understood compared to any other mammal. It has been instrumental in increasing our understanding of the vocalization systems of other mammals, including microbats. In the past, the human vocalization system was believed to be unique when compared to any of the other mammal vocalization system's, because of their ability to produce complex language and song. However, data has demonstrated that the human vocalization system is relatively similar to other mammal vocalization systems. A common theme that has been identified in all tetrapods, including humans and microbats: (1) a respiratory system with lungs; (2) a vocal tract that filters emitted sound before it exits into the surrounding environment; and (3) every tetrapod has a larynx that quickly closes to function in protection of the lungs, as well as it often might function in phonation, as is the case in humans and microbats. One feature of the mammal vocalization system that results in variation of sound production, especially for microbats and megabats, is the length of vocal folds. The vocal folds determine the lowest frequency at which the folds can vibrate. Compared to humans, the length of vocal folds in microbats are very small. This allows them to generate their characteristic ultrasonic waves that are above the human hearing range. In contrast, vocal folds of larger mammals, such as whales are greatly hypertrophied, which results in the production of infrasonic sounds far below the human hearing range.
Some moths have developed a protection against bats. They are able to hear bats' ultrasounds and flee as soon as they notice these sounds, or stop beating their wings for some time to deprive the bats of the characteristic echo signature of moving wings on which they may home in. To counteract this, the bats may cease producing the ultrasound bursts as they near prey, and thus avoid detection.
While bats have been traditionally divided into megabats and microbats, recent molecular evidence has shown the superfamily Rhinolophoidea to be more genetically related to megabats than to microbats, indicating the microbats are paraphyletic. To resolve the paraphyly of microbats, the Chiroptera were redivided into suborders Yangochiroptera (which includes Nycteridae, vespertilionoids, noctilionoids, and emballonuroids) and Yinpterochiroptera, which includes megabats, rhinopomatids, Rhinolophidae, and Megadermatidae.
This is the classification according to Simmons and Geisler (1998):
- Family Rhinopomatidae (mouse-tailed bats)
- Family Craseonycteridae (bumblebee bat or Kitti's hog-nosed bat)
- Family Rhinolophidae (horseshoe bats)
- Family Nycteridae (hollow-faced bats or slit-faced bats)
- Family Megadermatidae (false vampires)
- Family Natalidae (funnel-eared bats)
- Family Myzopodidae (sucker-footed bats)
- Family Thyropteridae (disk-winged bats)
- Family Furipteridae (smoky bats)
- Family Noctilionidae (bulldog bats or fisherman bats)
- Family Mystacinidae (New Zealand short-tailed bats)
- Family Mormoopidae (ghost-faced bats or moustached bats)
- Family Phyllostomidae (leaf-nosed bats)
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- Bat World Sanctuary
- Illustrated Identification key to the bats of Europe (see "Recent publications")
- Bat Conservation International
- View the myoLuc2 genome assembly in the UCSC Genome Browser.