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夜蛾的听觉系统。

Auditory system of noctuid moths.

作者信息

Roeder K D

出版信息

Science. 1966 Dec 23;154(3756):1515-21. doi: 10.1126/science.154.3756.1515.

Abstract

Insect-eating bats find their aerial food by sonar, through emitting ultrasonic chirps and locating sources of echoes. Certain moths have ears sensitive to these chirps and can detect bats well beyond the range of the bats' sonar. On hearing a distant bat, many moths turn and fly directly away from the source of ultrasound. Only one sense cell in each ear of a moth provides the primary nervous information for this response. This article describes my initial attempts to find out how a moth's central nervous system processes the train of chirps reaching its two ears. The ear of a restrained moth is exposed to a sequence of artifically generated ultrasonic pulses that approximates the cries made by a bat. This stimulus can be varied with respect to ultrasonic frequency (pitch), pulse intensity, pulse duration, the interval between pulses, and pulse-train duration. The more sensitive acoustic sense cell responds to all frequencies between about 15,000 and 80,000 cycles per second, but the signal that it transmits to the moth's central nervous system contains no measure of frequency within this range. However, this nerve signal reports variations in the other parameters of the stimulus. The acoustic fiber connects, in the central nervous system, with various nerve cells that transform the signal farther. The signal from a pulse-marker neuron contains no measures of pulse intensity or pulse duration, reporting only changes in interpulse interval and pulse-train duration. A train-marker neuron reports only the duration of the pulse train. The stimulus parameters may be likened to keys, each of which is necessary to gain admittance through a given door but becomes superfluous once this door has been passed. This analogy suggests one of the ways in which a signal is transformed in its passage through the nervous system, and how its specificity is assured in eliciting a given response. In addition to undergoing this kind of transformation, neural signals generated in the two directionally sensitive ears must be combined if a flying moth is to steer a course away from a distant bat. Neurons have been discovered in the central ganglia which summate signals from the right and left ears. Other neurons are inhibited in their activity by stimulation of one ear. The moth may combine signals from these neurons with motor-nerve information on the attitude of its own wings, which act as oscillating baffles modifying its directional acoustic sensitivity 20 to 40 times a second as it flaps an erratic path through the darkness.

摘要

食虫蝙蝠通过声呐寻找空中的食物,它们发出超声波啁啾并定位回声源。某些蛾类具有对这些啁啾敏感的耳朵,并且能够在蝙蝠声呐探测范围之外很好地察觉到蝙蝠。一听到远处有蝙蝠,许多蛾类就会转身直接飞离超声波源。蛾类每只耳朵中只有一个感觉细胞为这种反应提供主要的神经信息。本文描述了我最初尝试弄清楚蛾类中枢神经系统如何处理到达其两只耳朵的一连串啁啾声的过程。将一只被束缚的蛾类的耳朵暴露于一系列人工产生的超声波脉冲中,这些脉冲近似于蝙蝠发出的叫声。这种刺激在超声波频率(音高)、脉冲强度、脉冲持续时间、脉冲间隔以及脉冲序列持续时间方面可以有所变化。更敏感的听觉感觉细胞对每秒约15000至80000个周期之间的所有频率都有反应,但其传输到蛾类中枢神经系统的信号在此范围内不包含频率信息。然而,这个神经信号报告了刺激的其他参数的变化。听觉纤维在中枢神经系统中与各种进一步转换信号的神经细胞相连。来自脉冲标记神经元的信号不包含脉冲强度或脉冲持续时间的信息,只报告脉冲间隔和脉冲序列持续时间的变化。一个序列标记神经元只报告脉冲序列的持续时间。刺激参数可以比作钥匙(暗喻刺激参数的作用像钥匙开锁一样,每个参数在特定环节起作用,通过环节后就不再需要),每把钥匙都是打开特定一扇门所必需的,但一旦通过这扇门就变得多余了。这个比喻暗示了信号在通过神经系统时被转换的一种方式以及在引发特定反应时如何确保其特异性。除了经历这种转换之外,如果一只飞行中的蛾类要朝着远离远处蝙蝠的方向飞行,在两只具有方向敏感性的耳朵中产生的神经信号必须进行整合。在中枢神经节中已经发现了一些神经元,它们对来自右耳和左耳的信号进行总和。其他神经元在受到一只耳朵的刺激时其活动会受到抑制。蛾类可能会将来自这些神经元的信号与关于其自身翅膀姿态的运动神经信息相结合,其翅膀就像摆动的挡板,在它以不规则路径在黑暗中飞行时,每秒改变其方向声学敏感性20至40次。

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