Daubenton’s bats maintain stereotypical echolocation behaviour and a lombard response during target interception in light

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Accounts of Chemical Research Pub Date : 2024-04-29 DOI:10.1186/s40850-024-00200-4
Astrid Saermark Uebel, Michael Bjerre Pedersen, Kristian Beedholm, Laura Stidsholt, Marie Rosenkjaer Skalshøi, Ilias Foskolos, Peter Teglberg Madsen
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Abstract

Most bats hunt insects on the wing at night using echolocation as their primary sensory modality, but nevertheless maintain complex eye anatomy and functional vision. This raises the question of how and when insectivorous bats use vision during their largely nocturnal lifestyle. Here, we test the hypothesis that the small insectivorous bat, Myotis daubentonii, relies less on echolocation, or dispenses with it entirely, as visual cues become available during challenging acoustic noise conditions. We trained five wild-caught bats to land on a spherical target in both silence and when exposed to broad-band noise to decrease echo detectability, while light conditions were manipulated in both spectrum and intensity. We show that during noise exposure, the bats were almost three times more likely to use multiple attempts to solve the task compared to in silent controls. Furthermore, the bats exhibited a Lombard response of 0.18 dB/dBnoise and decreased call intervals earlier in their flight during masking noise exposures compared to in silent controls. Importantly, however, these adjustments in movement and echolocation behaviour did not differ between light and dark control treatments showing that small insectivorous bats maintain the same echolocation behaviour when provided with visual cues under challenging conditions for echolocation. We therefore conclude that bat echolocation is a hard-wired sensory system with stereotyped compensation strategies to both target range and masking noise (i.e. Lombard response) irrespective of light conditions. In contrast, the adjustments of call intervals and movement strategies during noise exposure varied substantially between individuals indicating a degree of flexibility that likely requires higher order processing and perhaps vocal learning.
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达本顿蝙蝠在光照下拦截目标时保持刻板的回声定位行为和伦巴第反应
大多数蝙蝠在夜间利用回声定位作为主要的感官模式在翼上捕食昆虫,但仍保持着复杂的眼部解剖结构和功能性视觉。这就提出了一个问题:食虫蝙蝠在其主要的夜间生活方式中如何以及何时使用视觉。在这里,我们验证了一个假设,即在具有挑战性的声学噪声条件下,当视觉线索可用时,小型食虫蝠会减少对回声定位的依赖,或者完全放弃回声定位。我们训练了五只野生捕获的蝙蝠在安静和暴露于宽带噪声以降低回声可探测性的情况下降落在球形目标上,同时在光谱和强度方面对光条件进行了调整。我们的研究表明,与安静对照组相比,在暴露于噪声时,蝙蝠通过多次尝试来完成任务的可能性几乎高出三倍。此外,与无声对照组相比,蝙蝠在掩蔽噪声暴露期间表现出 0.18 dB/dBnoise 的伦巴第反应,并在飞行早期减少了鸣叫间隔。但重要的是,这些运动和回声定位行为的调整在光照和黑暗对照处理之间并无差异,这表明小型食虫蝙蝠在回声定位挑战条件下获得视觉线索时仍能保持相同的回声定位行为。因此,我们得出结论,蝙蝠的回声定位是一种硬连接的感官系统,无论光照条件如何,都对目标范围和掩蔽噪声(即伦巴第反应)具有定型的补偿策略。与此相反,不同个体在暴露于噪声时对鸣叫间隔和运动策略的调整有很大差异,这表明蝙蝠具有一定程度的灵活性,这可能需要更高阶的处理过程,也可能需要声乐学习。
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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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