Summary: Motor areas of the cerebral cortex are dedicated to sonar production and wing control in Egyptian fruit bats.
Source: UC Davis
A new study shows how the brains of Egyptian fruit bats are highly specialized for echolocation and flight, with motor areas of the cerebral cortex that are dedicated to sonar production and wing control.
The work by researchers at UC Davis and UC Berkeley was published May 25 in Current Biology.
Professor Leah Krubitzer’s lab at the UC Davis Center for Neuroscience studies how evolution produces variation in brain organization across a wide variety of mammals, including opossums, tree shrews, rodents and primates. This comparative neurobiology approach shows how both evolution and development influence brain organization.
Although bats represent a quarter of all living mammalian species, this is the first time the full motor cortex of any bat has been mapped, said first author Andrew Halley, a postdoctoral researcher in Krubitzer’s lab.
The researchers used electrodes to stimulate different areas of the motor cortex in anesthetized bats to determine muscle and limb movements produced from stimulation. While classic theories of motor cortex organization assume individual muscles are represented in motor cortex, the new study found evidence for complex movements across diverse body regions.
“What we have found instead is that brain areas represent common synergies of muscles, rather than individual muscles,” Krubitzer said.
The Egyptian fruit bat (Rousettus aegyptiacus) is unusual among bats because it echolocates using its tongue, rather than its larynx (the latter being the method used by most echolocating bats). Egyptian fruit bats are known to have precise motor control of their tongue and are able to aim sonar beams in different directions simply by manipulating their tongues within their mouths, without moving their heads.
Correspondingly, the animal’s motor cortex has an unusually large region that represents movements of the tongue, Halley said. More than 40 percent of the sensory and motor cortex that was stimulated produced tongue movements — far more than in other species that have been studied, such as primates and rodents.
This study is part of a larger comparative project in Krubitzer’s laboratory that has shown motor regions of the brain are organized according to differences in their bodies and behaviors. “If you look at a rhesus macaque, a huge amount of the cortex is devoted to gripping,” Krubitzer said. Similarly, in humans, the hands are heavily represented.
Coordinating forelimbs and hindlimbs for flight
A bat’s wing is composed of membranes that spread across the “fingers” of its forelimb and back to its hindlimb and tail. Movement of any of these body parts can affect the shape of the wing and change the path of flight. The researchers found that few areas of motor cortex represented forelimb movement alone.
Instead, the vast majority of cortex represented synergistic shoulder and hindlimb movements. This reflects the fact that when these bats fly, the power for wing movement comes from shoulder muscles, while the fine adjustments needed for flying come from coordinated movements of shoulder and hindlimb muscles.
While forelimb movements were usually coupled with those of the hindlimb, other areas of cortex did produce movements of the hindlimb muscles alone. These are likely involved in the bats’ locomotor behaviors, “walking” around in trees by gripping branches with their hindlimbs.
Looking at brain organization in a wide variety of mammals helps us better understand our own brains, Krubitzer said.
“When we can look across species, it becomes a really powerful approach for making extrapolations to the human condition,” she said.
Additional coauthors on the study are: Mary Baldwin, Mackenzie Englund and Carlos Pineda at UC Davis; Dylan Cooke, Simon Fraser University, Canada; Tobias Schmid and Michael Yartsev, UC Berkeley. The work was partly supported by grants from the McDonnell Foundation and the National Institutes of Health, among others.
About this neuroscience research news
Author: Andrew Fell
Source: UC Davis
Contact: Andrew Fell – UC Davis
Image: The image is in the public domain
Original Research: Open access.
“Coevolution of motor cortex and behavioral specializations associated with flight and echolocation in bats” by Leah Krubitzer et al. Current Biology
Coevolution of motor cortex and behavioral specializations associated with flight and echolocation in bats
- The first motor map of any bat species using intracortical microstimulation
- Rousettus, a lingual echolocating bat, has an enlarged tongue motor representation
- Forelimb movements are usually coupled with hindlimb movements
- Motor organization is consistent with adaptations for flight and echolocation
Bats have evolved behavioral specializations that are unique among mammals, including self-propelled flight and echolocation. However, areas of motor cortex that are critical in the generation and fine control of these unique behaviors have never been fully characterized in any bat species, despite the fact that bats compose ∼25% of extant mammalian species.
Using intracortical microstimulation, we examined the organization of motor cortex in Egyptian fruit bats (Rousettus aegyptiacus), a species that has evolved a novel form of tongue-based echolocation.
We found that movement representations include an enlarged tongue region containing discrete subregions devoted to generating distinct tongue movement types, consistent with their behavioral specialization generating active sonar using tongue clicks. This magnification of the tongue in motor cortex is comparable to the enlargement of somatosensory representations in species with sensory specializations.
We also found a novel degree of coactivation between the forelimbs and hindlimbs, both of which are involved in altering the shape and tension of wing membranes during flight.
Together, these findings suggest that the organization of motor cortex has coevolved with peripheral morphology in bats to support the unique motor demands of flight and echolocation.