Bats fly with breathtaking precision because their wings are equipped with highly sensitive touch sensors¹, cells that respond to even slight changes in airflow, researchers have demonstrated for the first time. Scientists from Johns Hopkins University, as well as Columbia University and the University of Maryland, determined² how the sense of touch plays a key role in powered flight. In a paper published April 30 in the journal Cell Reports, they show how sensory³ receptors in bat wings send information about airflow to neurons in the brain, enabling the bat to make split-second flight control adjustments.

 

"Until now no one had investigated the sensors on the bat's wing, which allow it to serve as more than a propeller⁴, a flipper⁵, an airplane wing or any simple airfoil," said Johns Hopkins neuroscientist Cynthia F. Moss⁶, one of the senior authors and a professor in the Department of Psychological and Brain Sciences in the Krieger School of Arts and Sciences. "These findings can inform more broadly how organisms use touch to guide movement."

 

Moss and the team studied the big brown bat, a common species found throughout North America. Bats are the only mammals capable of true powered flight, able to reach speeds of 7 to 20 mph with the sort of aerial maneuverability humans only wish they could engineer.

 

The team found that the evolutionary⁷ process that allowed bats to form wings resulted in unusual tactile⁸ circuitry that not only enhances control during flight, but also allows bats to use their wings to climb, cradle their young and capture insects.

 

First, they discovered an array of sensory receptors in bat wings -- a significant number of which are clustered at the base of tiny hairs that cover the appendages⁹. That placement of these touch cells, both lanceolate endings and Merkel cells, allows the bat, while flying, to sense changes in airflow as air ruffles¹⁰ the hairs.

 

When the team stimulated¹¹ these hairs with brief air puffs¹², neurons in the bat's primary somatosensory cortex responded with precisely¹³ timed but sparse¹⁴ bursts of activity, suggesting this circuitry helped guide bats during fast, dynamic flight.

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