孵化与不孵化:前庭机械感应起始阶段的异时性是否能解释蛇类攻击中Agalychnis胚胎逃逸孵化成功率的物种差异?

IF 1.9 2区 生物学 Q3 BEHAVIORAL SCIENCES
Brandon A. Güell, Karen M. Warkentin
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引用次数: 0

摘要

摘要叶绿体树蛙过早孵化以躲避卵的捕食,但不同物种的躲避成功率不同。蛇的攻击导致自发孵化的Agalychnis spurrelli的逃逸孵化率比发育较差的Agalychnis callidryas低55%。茧蛙利用前庭系统,其次是侧线来感知提示孵化的物理干扰。由于马氏茧蝶的发育速度较快,我们推测,相对于孵化能力而言,前庭机械感觉功能的开始时间的异时性变化可能是它们对机械感觉线索的逃逸反应较低的原因。为了验证这一观点,我们比较了缺氧和机械感觉诱导孵化(MCH)的起始时间,以及两个物种发育序列中前庭机械感觉功能的起始时间。在不同的物种中,大多数同胞在相同的发育阶段开始对每种提示做出反应,而通过前庭眼反射(VOR)测量的前庭功能发育也很相似。这些结果表明,马刺秧鸡逃逸孵化成功率低并不是因为前庭机械感觉功能的起始延迟造成的。马刺蛙的 MCH 起始与 VOR 有关,但阈值比马刺蛙高。在强大的前庭功能之前没有 MCH 的现象表明,多模式机械感应可能不会对 A. spurrelli 胚胎的反捕食者反应做出贡献。我们的观察结果表明,在蛇的攻击下,较大的卵团的逃逸成功率较高,而在淹水的马刺秧鸡中,孵化并发症较多,这表明卵团和卵囊结构的差异可能直接导致了逃逸-孵化成功率的物种差异。此外,水刺蛇的孵化并发症可能会选择性地避免错误警报,从而提高孵化决策规则的严格程度。对某些物种而言,孵化也是抵御卵期风险的有效防御手段。然而,人们对环境暗示孵化反应差异的原因知之甚少。我们评估了为什么两种亲缘关系很近的树蛙对蛇的攻击表现出不同的逃逸-孵化反应。比较Agalychnis callidryas和A. spurrelli的诱导孵化反应开始时间和前庭功能发现,机械感应的主要机制及其发育时间在该类群中是一致的,但行为反应的感觉功能阈值却不同。研究还发现,卵螯的特性,包括卵螯的大小和单个卵的结构,会影响逃逸-孵化反应。这促使我们进一步研究评估卵离合器特性及其生物力学在胚胎逃逸-孵化反应中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

To hatch and hatch not: does heterochrony in onset of vestibular mechanosensing explain species differences in escape-hatching success of Agalychnis embryos in snake attacks?

To hatch and hatch not: does heterochrony in onset of vestibular mechanosensing explain species differences in escape-hatching success of Agalychnis embryos in snake attacks?

Abstract

Phyllomedusid treefrogs hatch prematurely to escape egg predation, but escape success varies among species. Snake attacks elicited 55% less escape hatching in spontaneously hatching Agalychnis spurrelli than in less developed A. callidryas. Agalychnis callidryas use their vestibular system and, secondarily, their lateral line to sense physical disturbances that cue hatching. Since A. spurrelli develop faster, we hypothesized that heterochronic shifts in the onset timing of vestibular mechanosensory function, relative to hatching ability, might explain their lower escape response to mechanosensory cues. To test this, we compared onset timings of hypoxia- and mechanosensory-cued hatching (MCH) and vestibular mechanosensory function in developmental series of both species. Across species, most sibships began responding to each cue at the same developmental stage and vestibular function development, measured by the vestibulo-ocular reflex (VOR), was similar. These results demonstrate that low escape-hatching success in A. spurrelli is not caused by a delay in the onset of vestibular mechanosensory function. MCH onset in A. spurrelli was associated with VOR, but with a higher threshold than in A. callidryas. The absence of MCH before strong vestibular function suggests multimodal mechanosensing may not contribute to antipredator responses of A. spurrelli embryos. Our observations of higher escape success of larger clutches in snake attacks and hatching complications in flooded A. spurrelli suggest that differences in clutch and egg capsule structure may contribute directly to species differences in escape-hatching success. Moreover, hatching complications in A. spurrelli may select against false alarms, increasing the stringency of hatching decision rules.

Significance statement

Hatching is an essential life-stage transition during development. For some species, it also functions as an effective defense against egg-stage risks. However, the causes for variation in environmentally cued hatching responses are poorly understood. We assessed why two closely related treefrogs exhibit different escape-hatching responses to snake attacks. Comparing the onset of induced-hatching responses and vestibular function in Agalychnis callidryas and A. spurrelli revealed that the primary mechanism for mechanosensing and its developmental timing are conserved within this group, but the sensory function threshold for behavioral response differs. It also revealed that egg-clutch properties, including egg-clutch size and individual egg structure, affect the escape-hatching response. This motivates further research assessing the role of egg-clutch properties and their biomechanics in embryo escape-hatching responses.

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来源期刊
CiteScore
3.90
自引率
8.70%
发文量
146
审稿时长
3 months
期刊介绍: The journal publishes reviews, original contributions and commentaries dealing with quantitative empirical and theoretical studies in the analysis of animal behavior at the level of the individual, group, population, community, and species.
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