Hindlimb kinematics, kinetics, and muscle dynamics during sit-to-stand and sit-to-walk transitions in emus (Dromaius novaehollandiae).

IF 2.8 2区 生物学 Q2 BIOLOGY Journal of Experimental Biology Pub Date : 2024-10-24 DOI:10.1242/jeb.247519
Yuting Lin, Jeffery W Rankin, Luís P Lamas, Mehran Moazen, John R Hutchinson
{"title":"Hindlimb kinematics, kinetics, and muscle dynamics during sit-to-stand and sit-to-walk transitions in emus (Dromaius novaehollandiae).","authors":"Yuting Lin, Jeffery W Rankin, Luís P Lamas, Mehran Moazen, John R Hutchinson","doi":"10.1242/jeb.247519","DOIUrl":null,"url":null,"abstract":"<p><p>Terrestrial animals not only need to walk and run but also lie prone to rest and then stand up. Sit-to-stand (STS) and sit-to-walk (STW) transitions are vital behaviours little studied in species other than humans so far, but likely impose biomechanical constraints on limb design because they involve near-maximal excursions of limb joints that should require large length changes and force production from muscles. By integrating data from experiments into musculoskeletal simulations, we analysed joint motions, ground reaction forces, and muscle dynamics during STS and STW in a large terrestrial, bipedal, and cursorial bird: the emu (Dromaius novaehollandiae, ∼30 kg). Simulation results suggest that in both STS and STW, emus operate near the functional limits (∼50 % of shortening/lengthening) of some of their hindlimb muscles, particularly in distal muscles with limited capacity for length change and leverage. Both movements involved high muscle activations (> 50 %) and force generation of the major joint extensor muscles early in the transition. STW required larger net joint moments and non-sagittal motions than STS, entailing greater demands for muscle capacity. Whilst our study involves multiple assumptions, our findings lay the groundwork for future studies to understand, for example, how tendon contributions may reduce excessive muscle demands, especially in the distal hindlimb. As the first investigation into how an avian species stands up, this study provides a foundational framework for future comparative studies investigating organismal morphofunctional specialisations and evolution, offering potential robotics and animal welfare applications.</p>","PeriodicalId":15786,"journal":{"name":"Journal of Experimental Biology","volume":null,"pages":null},"PeriodicalIF":2.8000,"publicationDate":"2024-10-24","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.247519","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

Terrestrial animals not only need to walk and run but also lie prone to rest and then stand up. Sit-to-stand (STS) and sit-to-walk (STW) transitions are vital behaviours little studied in species other than humans so far, but likely impose biomechanical constraints on limb design because they involve near-maximal excursions of limb joints that should require large length changes and force production from muscles. By integrating data from experiments into musculoskeletal simulations, we analysed joint motions, ground reaction forces, and muscle dynamics during STS and STW in a large terrestrial, bipedal, and cursorial bird: the emu (Dromaius novaehollandiae, ∼30 kg). Simulation results suggest that in both STS and STW, emus operate near the functional limits (∼50 % of shortening/lengthening) of some of their hindlimb muscles, particularly in distal muscles with limited capacity for length change and leverage. Both movements involved high muscle activations (> 50 %) and force generation of the major joint extensor muscles early in the transition. STW required larger net joint moments and non-sagittal motions than STS, entailing greater demands for muscle capacity. Whilst our study involves multiple assumptions, our findings lay the groundwork for future studies to understand, for example, how tendon contributions may reduce excessive muscle demands, especially in the distal hindlimb. As the first investigation into how an avian species stands up, this study provides a foundational framework for future comparative studies investigating organismal morphofunctional specialisations and evolution, offering potential robotics and animal welfare applications.

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
鸸鹋(Dromaius novaehollandiae)从坐到站和从坐到走的转变过程中的后肢运动学、动力学和肌肉动力学。
陆生动物不仅需要行走和奔跑,还需要俯卧休息,然后站立起来。从坐到站(STS)和从坐到走(STW)的转换是除人类以外的其他物种的重要行为,但迄今为止对它们的研究很少,但它们很可能对肢体设计造成生物力学限制,因为它们涉及肢体关节的近最大偏移,需要肌肉产生较大的长度变化和力量。通过将实验数据整合到肌肉骨骼模拟中,我们分析了鸸鹋(Dromaius novaehollandiae,体重∼30 千克)这种大型陆生两足草食性鸟类在 STS 和 STW 期间的关节运动、地面反作用力和肌肉动力学。模拟结果表明,在STS和STW运动中,鸸鹋的部分后肢肌肉接近功能极限(缩短/延长50%),尤其是长度变化和杠杆作用能力有限的远端肌肉。这两个动作在过渡的早期都涉及主要关节伸肌的高肌肉激活(> 50%)和发力。STW 比 STS 需要更大的净关节力矩和非矢状运动,对肌肉能力的要求更高。虽然我们的研究涉及多种假设,但我们的发现为今后的研究奠定了基础,例如,了解肌腱的贡献如何减少对肌肉的过度需求,特别是在后肢远端。作为对鸟类物种如何站立的首次调查,本研究为未来调查生物体形态功能特化和进化的比较研究提供了一个基础框架,为机器人和动物福利应用提供了可能性。
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
How do fish miss? Attack strategies of threespine stickleback capturing non-evasive prey. Hypertonic water reabsorption with a parallel-current system via the glandular and saccular renal tubules of Ruditapes philippinarum. Skittering locomotion in cricket frogs: a form of porpoising. Investigating in vivo force and work production of rat medial gastrocnemius at varying locomotor speeds using a muscle avatar. Bridging the divide in organismal physiology: a case for the integration of behaviour as a physiological process.
×
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