Flexibility of cutaneous evaporative water loss in response to hydration in pregnant Prairie Rattlesnakes (Crotalus viridis) and their neonates.

IF 2.8 2区 生物学 Q2 BIOLOGY Journal of Experimental Biology Pub Date : 2024-12-13 DOI:10.1242/jeb.247964
Robin E Bedard, Savannah J Weaver, Haley A Moniz, Scott M Boback, Emily N Taylor
{"title":"Flexibility of cutaneous evaporative water loss in response to hydration in pregnant Prairie Rattlesnakes (Crotalus viridis) and their neonates.","authors":"Robin E Bedard, Savannah J Weaver, Haley A Moniz, Scott M Boback, Emily N Taylor","doi":"10.1242/jeb.247964","DOIUrl":null,"url":null,"abstract":"<p><p>Viviparous snakes may be particularly vulnerable to predicted increases in drought due to the high hydric costs associated with embryonic development, gestation, and their reliance on limited free-standing bodies of water or rain events for hydration. Drought will have negative implications for viper populations if females become increasingly water-stressed and resorb developing embryos to conserve bodily water. We conducted a study to investigate the importance of drinking water in late-term pregnancy and its effect on cutaneous evaporative water loss (CEWL). We measured hydration and water loss in response to supplemental hydration during the final stages of embryonic development and gestation in arid-adapted Prairie Rattlesnakes (Crotalus viridis). Our goal was to assess how supplemental water affects hydration status and water loss (via CEWL) of females during and after pregnancy, and of their neonates before and after their first ecdysis. Supplemental hydration of pregnant C. viridis improved their hydration state and their neonates were also born more hydrated than those from control mothers, showing that they transfer water to neonates via the placenta even over a very short period in the late stages of pregnancy. The supplementally hydrated maternal C. viridis experienced slightly higher rates of CEWL compared to control snakes, but CEWL was primarily driven by ambient temperature and vapor pressure deficit at the time of measurement. At birth, neonate plasma osmolality and CEWL were both directly associated with their mothers' plasma osmolality and CEWL. Additionally, we found that neonate CEWL increased after the first ecdysis, suggesting that natal skin may help neonates avoid desiccation. Investigating and quantifying physiological implications of water shortage and dehydration can help us better understand the effects of drought and predict how wild populations of arid-adapted reptiles may respond to the predicted increase in frequency and severity of droughts.</p>","PeriodicalId":15786,"journal":{"name":"Journal of Experimental Biology","volume":" ","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2024-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Experimental Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1242/jeb.247964","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Viviparous snakes may be particularly vulnerable to predicted increases in drought due to the high hydric costs associated with embryonic development, gestation, and their reliance on limited free-standing bodies of water or rain events for hydration. Drought will have negative implications for viper populations if females become increasingly water-stressed and resorb developing embryos to conserve bodily water. We conducted a study to investigate the importance of drinking water in late-term pregnancy and its effect on cutaneous evaporative water loss (CEWL). We measured hydration and water loss in response to supplemental hydration during the final stages of embryonic development and gestation in arid-adapted Prairie Rattlesnakes (Crotalus viridis). Our goal was to assess how supplemental water affects hydration status and water loss (via CEWL) of females during and after pregnancy, and of their neonates before and after their first ecdysis. Supplemental hydration of pregnant C. viridis improved their hydration state and their neonates were also born more hydrated than those from control mothers, showing that they transfer water to neonates via the placenta even over a very short period in the late stages of pregnancy. The supplementally hydrated maternal C. viridis experienced slightly higher rates of CEWL compared to control snakes, but CEWL was primarily driven by ambient temperature and vapor pressure deficit at the time of measurement. At birth, neonate plasma osmolality and CEWL were both directly associated with their mothers' plasma osmolality and CEWL. Additionally, we found that neonate CEWL increased after the first ecdysis, suggesting that natal skin may help neonates avoid desiccation. Investigating and quantifying physiological implications of water shortage and dehydration can help us better understand the effects of drought and predict how wild populations of arid-adapted reptiles may respond to the predicted increase in frequency and severity of droughts.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
妊娠草原响尾蛇(Crotalus viridis)及其幼蛇对水合反应中皮肤蒸发水分损失的灵活性。
由于胚胎发育和妊娠过程中需要付出高昂的水力成本,并且依赖于有限的独立水体或降雨来补充水分,因此胎生蛇类可能特别容易受到预计干旱加剧的影响。如果雌性蝰蛇变得越来越缺水,并吸收发育中的胚胎以保存体内水分,那么干旱将对蝰蛇种群产生负面影响。我们进行了一项研究,以调查妊娠晚期饮水的重要性及其对皮肤蒸发失水(CEWL)的影响。我们测量了适应干旱环境的草原响尾蛇(Crotalus viridis)在胚胎发育和妊娠的最后阶段补充水分时的水合作用和失水情况。我们的目标是评估补充水如何影响雌蛇在怀孕期间和之后的水合状态和失水(通过 CEWL),以及新生儿在第一次蜕皮之前和之后的水合状态和失水(通过 CEWL)。给怀孕的雌性 C. viridis 补充水分改善了它们的水合状态,与对照组相比,它们的新生儿出生时的水合状态也更好,这表明即使在怀孕后期很短的时间内,雌性 C. viridis 也能通过胎盘将水分转移给新生儿。与对照组蛇类相比,补充水分的母蛇C. viridis的CEWL率略高,但CEWL主要受测量时的环境温度和蒸汽压不足的影响。新生儿出生时的血浆渗透压和CEWL都与其母亲的血浆渗透压和CEWL直接相关。此外,我们还发现新生儿的CEWL在第一次蜕皮后有所增加,这表明新生儿出生时的皮肤可能有助于新生儿避免干燥。对缺水和脱水的生理影响进行研究和量化有助于我们更好地了解干旱的影响,并预测适应干旱的爬行动物野生种群可能会如何应对预计的干旱频率和严重程度的增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
5.50
自引率
10.70%
发文量
494
审稿时长
1 months
期刊介绍: Journal of Experimental Biology is the leading primary research journal in comparative physiology and publishes papers on the form and function of living organisms at all levels of biological organisation, from the molecular and subcellular to the integrated whole animal.
期刊最新文献
Light alters calling-song characteristics in crickets. Multispecies comparisons support a startle response origin for a novel vibrational signal in the cricket tribe Lebinthini. WildPose: A long-range 3D wildlife motion capture system. Towards a standard application of the Reynolds number in studies of aquatic animal locomotion. Allatostatin-C signaling in the crab, Carcinus maenas is implicated in the ecdysis programme.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1