非洲爪蛙蝌蚪的空气呼吸机制,非洲爪蛙(无尾目:蝌蚪科)。

Jackson R. Phillips, A. Hewes, Molly C. Womack, K. Schwenk
{"title":"非洲爪蛙蝌蚪的空气呼吸机制,非洲爪蛙(无尾目:蝌蚪科)。","authors":"Jackson R. Phillips, A. Hewes, Molly C. Womack, K. Schwenk","doi":"10.1242/jeb.243102","DOIUrl":null,"url":null,"abstract":"Frog larvae (tadpoles) undergo many physiological, morphological, and behavioral transformations through development before metamorphosing into their adult form. The surface tension of water prevents small tadpoles from breaching the surface to breathe air (including those of Xenopus laevis), forcing them to acquire air using a form of breathing called bubble-sucking. With growth, tadpoles typically make a behavioral/biomechanical transition). X. laevis tadpoles have also been shown to transition physiologically from conforming passively to ambient oxygen levels to actively regulating their blood oxygen. However, it is unknown whether these mechanical and physiological breathing transitions are temporally or functionally linked, or how both transitions relate to lung maturation and gas exchange competency. If these transitions are linked, it could mean that one biomechanical breathing mode (breaching) is more physiologically proficient at acquiring gaseous oxygen than the other. Here, we describe the mechanics and development of air-breathing and the ontogeny of lung morphology in X. laevis throughout the larval stage and examine our findings considering previous physiological work. We find that the transitions from bubble-sucking to breaching and from oxygen conforming to oxygen regulation co-occur in X. laevis tadpoles at the same larval stage (Nieuwkoop-Faber stages 53-56 and 54-57, respectively), but that the lungs do not increase significantly in vascularization until metamorphosis, suggesting that lung maturation, alone, is not sufficient to account for increased pulmonary capacity earlier in development. Although breach-breathing may confer a respiratory advantage, we remain unaware of a mechanistic explanation to account for this possibility. At present, the transition from bubble-sucking to breaching appears simply to be a consequence of growth. Finally, we consider our results in the context of comparative air-breathing mechanics across vertebrates.","PeriodicalId":22458,"journal":{"name":"THE EGYPTIAN JOURNAL OF EXPERIMENTAL BIOLOGY","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"The mechanics of air-breathing in African clawed frog tadpoles, Xenopus laevis (Anura: Pipidae).\",\"authors\":\"Jackson R. Phillips, A. Hewes, Molly C. Womack, K. Schwenk\",\"doi\":\"10.1242/jeb.243102\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Frog larvae (tadpoles) undergo many physiological, morphological, and behavioral transformations through development before metamorphosing into their adult form. The surface tension of water prevents small tadpoles from breaching the surface to breathe air (including those of Xenopus laevis), forcing them to acquire air using a form of breathing called bubble-sucking. With growth, tadpoles typically make a behavioral/biomechanical transition). X. laevis tadpoles have also been shown to transition physiologically from conforming passively to ambient oxygen levels to actively regulating their blood oxygen. However, it is unknown whether these mechanical and physiological breathing transitions are temporally or functionally linked, or how both transitions relate to lung maturation and gas exchange competency. If these transitions are linked, it could mean that one biomechanical breathing mode (breaching) is more physiologically proficient at acquiring gaseous oxygen than the other. Here, we describe the mechanics and development of air-breathing and the ontogeny of lung morphology in X. laevis throughout the larval stage and examine our findings considering previous physiological work. We find that the transitions from bubble-sucking to breaching and from oxygen conforming to oxygen regulation co-occur in X. laevis tadpoles at the same larval stage (Nieuwkoop-Faber stages 53-56 and 54-57, respectively), but that the lungs do not increase significantly in vascularization until metamorphosis, suggesting that lung maturation, alone, is not sufficient to account for increased pulmonary capacity earlier in development. Although breach-breathing may confer a respiratory advantage, we remain unaware of a mechanistic explanation to account for this possibility. At present, the transition from bubble-sucking to breaching appears simply to be a consequence of growth. Finally, we consider our results in the context of comparative air-breathing mechanics across vertebrates.\",\"PeriodicalId\":22458,\"journal\":{\"name\":\"THE EGYPTIAN JOURNAL OF EXPERIMENTAL BIOLOGY\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-04-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"THE EGYPTIAN JOURNAL OF EXPERIMENTAL BIOLOGY\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1242/jeb.243102\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"THE EGYPTIAN JOURNAL OF EXPERIMENTAL BIOLOGY","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1242/jeb.243102","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

摘要

青蛙的幼虫(蝌蚪)在发育过程中经历了许多生理、形态和行为上的变化,然后才变成成虫。水的表面张力阻止小蝌蚪突破水面呼吸空气(包括非洲爪蟾),迫使它们通过一种叫做吸泡的呼吸方式获得空气。随着成长,蝌蚪通常会进行行为/生物力学的转变)。X. laevis蝌蚪也被证明在生理上从被动地适应环境氧水平转变为主动调节血氧。然而,尚不清楚这些机械和生理呼吸转变是否在时间上或功能上相关,也不清楚这两种转变如何与肺成熟和气体交换能力相关。如果这些转变是联系在一起的,这可能意味着一种生物力学呼吸模式(突破)在生理上比另一种更擅长获取气态氧气。在这里,我们描述了在整个幼虫期的空气呼吸机制和发展以及肺形态的个体发生,并结合先前的生理工作来检验我们的发现。我们发现,在同一幼虫期(nieuwkop - faber阶段分别为53-56和54-57),X. laevis蝌蚪同时发生从吸泡到破裂和从氧气到氧气调节的转变,但肺血管化直到变形才显著增加,这表明肺成熟本身不足以解释发育早期肺容量的增加。虽然间歇呼吸可能会给呼吸带来好处,但我们仍然没有意识到一个机械的解释来解释这种可能性。目前,从吸泡到破泡的转变似乎只是经济增长的结果。最后,我们在比较脊椎动物的空气呼吸力学的背景下考虑我们的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The mechanics of air-breathing in African clawed frog tadpoles, Xenopus laevis (Anura: Pipidae).
Frog larvae (tadpoles) undergo many physiological, morphological, and behavioral transformations through development before metamorphosing into their adult form. The surface tension of water prevents small tadpoles from breaching the surface to breathe air (including those of Xenopus laevis), forcing them to acquire air using a form of breathing called bubble-sucking. With growth, tadpoles typically make a behavioral/biomechanical transition). X. laevis tadpoles have also been shown to transition physiologically from conforming passively to ambient oxygen levels to actively regulating their blood oxygen. However, it is unknown whether these mechanical and physiological breathing transitions are temporally or functionally linked, or how both transitions relate to lung maturation and gas exchange competency. If these transitions are linked, it could mean that one biomechanical breathing mode (breaching) is more physiologically proficient at acquiring gaseous oxygen than the other. Here, we describe the mechanics and development of air-breathing and the ontogeny of lung morphology in X. laevis throughout the larval stage and examine our findings considering previous physiological work. We find that the transitions from bubble-sucking to breaching and from oxygen conforming to oxygen regulation co-occur in X. laevis tadpoles at the same larval stage (Nieuwkoop-Faber stages 53-56 and 54-57, respectively), but that the lungs do not increase significantly in vascularization until metamorphosis, suggesting that lung maturation, alone, is not sufficient to account for increased pulmonary capacity earlier in development. Although breach-breathing may confer a respiratory advantage, we remain unaware of a mechanistic explanation to account for this possibility. At present, the transition from bubble-sucking to breaching appears simply to be a consequence of growth. Finally, we consider our results in the context of comparative air-breathing mechanics across vertebrates.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信