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Regulation of Heat Exchange across the Hornbill Beak: Functional Similarities with Toucans?

机译:犀鸟喙的热交换调节:与巨嘴鸟的功能相似吗?

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Beaks are increasingly recognised as important contributors to avian thermoregulation. Several studies supporting Allen’s rule demonstrate how beak size is under strong selection related to latitude and/or air temperature (Ta). Moreover, active regulation of heat transfer from the beak has recently been demonstrated in a toucan (Ramphastos toco, Ramphastidae), with the large beak acting as an important contributor to heat dissipation. We hypothesised that hornbills (Bucerotidae) likewise use their large beaks for non-evaporative heat dissipation, and used thermal imaging to quantify heat exchange over a range of air temperatures in eighteen desert-living Southern Yellow-billed Hornbills (Tockus leucomelas). We found that hornbills dissipate heat via the beak at air temperatures between 30.7°C and 41.4°C. The difference between beak surface and environmental temperatures abruptly increased when air temperature was within ~10°C below body temperature, indicating active regulation of heat loss. Maximum observed heat loss via the beak was 19.9% of total non-evaporative heat loss across the body surface. Heat loss per unit surface area via the beak more than doubled at Ta 30.7°C compared to Ta 30.7°C and at its peak dissipated 25.1 W m-2. Maximum heat flux rate across the beak of toucans under comparable convective conditions was calculated to be as high as 61.4 W m-2. The threshold air temperature at which toucans vasodilated their beak was lower than that of the hornbills, and thus had a larger potential for heat loss at lower air temperatures. Respiratory cooling (panting) thresholds were also lower in toucans compared to hornbills. Both beak vasodilation and panting threshold temperatures are potentially explained by differences in acclimation to environmental conditions and in the efficiency of evaporative cooling under differing environmental conditions. We speculate that non-evaporative heat dissipation may be a particularly important mechanism for animals inhabiting humid regions, such as toucans, and less critical for animals residing in more arid conditions, such as Southern Yellow-billed Hornbills. Alternatively, differences in beak morphology and hardness enforced by different diets may affect the capacity of birds to use the beak for non-evaporative heat loss.
机译:喙越来越被认为是禽类体温调节的重要因素。多项支持艾伦法则的研究表明,在强烈选择纬度和/或气温(Ta)的情况下,喙的大小是如何选择的。此外,最近已在巨嘴鸟(Ramphastos toco,Ramphastidae)中证明了从喙进行传热的主动调节,其中大喙是散热的重要因素。我们假设犀鸟(Bucerotidae)同样使用它们的大喙进行非蒸发式散热,并使用热成像技术来量化十八个沙漠生活的南部黄嘴犀鸟(Tockus leucomelas)在一定温度范围内的热交换。我们发现,犀鸟在30.7°C至41.4°C的气温下通过喙散热。当气温低于体温约10°C以内时,喙表面和环境温度之间的差异会突然增加,这表明热量的主动调节。通过喙观察到的最大热损失是整个身体表面非蒸发热损失的19.9%。与Ta <30.7°C相比,Ta> 30.7°C时通过喙的单位表面积的热损失增加了一倍以上,并且在其峰值处耗散25.1 W m-2。在相当的对流条件下,整个巨嘴鸟喙的最大热通量计算值高达61.4 W m-2。巨嘴鸟使喙喙血管扩张的阈值空气温度低于犀鸟,因此在较低的温度下具有更大的热损失潜能。与犀鸟相比,巨嘴鸟的呼吸冷却(气喘)阈值也较低。喙血管舒张和气喘阈值温度都可能通过适应环境条件和在不同环境条件下蒸发冷却的效率差异来解释。我们推测,非蒸发散热可能是居住在潮湿地区(例如巨嘴鸟)的动物的一个特别重要的机制,而对于居住在更干旱条件下的动物(例如南部黄嘴犀鸟)而言则不是那么重要。另外,不同饮食所引起的喙形态和硬度的差异可能会影响禽鸟利用喙进行非蒸发热损失的能力。

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