Bone microstructure supports a Mesozoic origin for a semiaquatic burrowing lifestyle in monotremes (Mammalia)

IF 9.4 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Suzanne J. Hand, Laura A. B. Wilson, Camilo López-Aguirre, Alexandra Houssaye, Michael Archer, Joseph J. Bevitt, Alistair R. Evans, Amalia Y. Halim, Tzong Hung, Thomas H. Rich, Patricia Vickers-Rich, Robin M. D. Beck
{"title":"Bone microstructure supports a Mesozoic origin for a semiaquatic burrowing lifestyle in monotremes (Mammalia)","authors":"Suzanne J. Hand, Laura A. B. Wilson, Camilo López-Aguirre, Alexandra Houssaye, Michael Archer, Joseph J. Bevitt, Alistair R. Evans, Amalia Y. Halim, Tzong Hung, Thomas H. Rich, Patricia Vickers-Rich, Robin M. D. Beck","doi":"10.1073/pnas.2413569122","DOIUrl":null,"url":null,"abstract":"The platypus and four echidna species are the only living egg-laying mammals and the sole extant representatives of Order Monotremata. The platypus and echidnas are very disparate both morphologically and ecologically: The platypus is a specialized semiaquatic burrowing form that forages for freshwater invertebrates, whereas echidnas are fully terrestrial and adapted for feeding on social insects and earthworms. It has been proposed that echidnas evolved from a semiaquatic, platypus-like ancestor, but fossil evidence for such a profound evolutionary transformation has been lacking, and this hypothesis remains controversial. Here, we present original data about the Early Cretaceous (108 to 103 Ma) Australian mammal <jats:italic>Kryoryctes cadburyi</jats:italic> , currently only known from a single humerus, that provides key information relating to this question. Phylogenetic analysis of a 536-character morphological matrix of mammaliaforms places <jats:italic>Kryoryctes</jats:italic> as a stem-monotreme. Three-dimensional whole bone comparisons show that the overall shape of the humerus is more similar to that of echidnas than the platypus, but analysis of microstructure reveals specializations found in semiaquatic mammals, including a particularly thick cortex and a highly reduced medullary cavity, present in the platypus but absent in echidnas. The evidence suggests <jats:italic>Kryoryctes</jats:italic> was a semiaquatic burrower, indicating that monotremes first evolved an amphibious lifestyle in the Mesozoic, and providing support for the hypothesis that this is ancestral for living monotremes as a whole. The lineage leading to the modern platypus appears to have been characterized by extremely long term (&gt;100 My) niche conservatism, with echidnas representing a much later reversion to a fully terrestrial lifestyle.","PeriodicalId":20548,"journal":{"name":"Proceedings of the National Academy of Sciences of the United States of America","volume":"52 1","pages":""},"PeriodicalIF":9.4000,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of the National Academy of Sciences of the United States of America","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1073/pnas.2413569122","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

The platypus and four echidna species are the only living egg-laying mammals and the sole extant representatives of Order Monotremata. The platypus and echidnas are very disparate both morphologically and ecologically: The platypus is a specialized semiaquatic burrowing form that forages for freshwater invertebrates, whereas echidnas are fully terrestrial and adapted for feeding on social insects and earthworms. It has been proposed that echidnas evolved from a semiaquatic, platypus-like ancestor, but fossil evidence for such a profound evolutionary transformation has been lacking, and this hypothesis remains controversial. Here, we present original data about the Early Cretaceous (108 to 103 Ma) Australian mammal Kryoryctes cadburyi , currently only known from a single humerus, that provides key information relating to this question. Phylogenetic analysis of a 536-character morphological matrix of mammaliaforms places Kryoryctes as a stem-monotreme. Three-dimensional whole bone comparisons show that the overall shape of the humerus is more similar to that of echidnas than the platypus, but analysis of microstructure reveals specializations found in semiaquatic mammals, including a particularly thick cortex and a highly reduced medullary cavity, present in the platypus but absent in echidnas. The evidence suggests Kryoryctes was a semiaquatic burrower, indicating that monotremes first evolved an amphibious lifestyle in the Mesozoic, and providing support for the hypothesis that this is ancestral for living monotremes as a whole. The lineage leading to the modern platypus appears to have been characterized by extremely long term (>100 My) niche conservatism, with echidnas representing a much later reversion to a fully terrestrial lifestyle.
骨骼微观结构支持单孔目动物(哺乳动物)半水生穴居生活方式的中生代起源
鸭嘴兽和四种针鼹是唯一活着的卵生哺乳动物,也是单喉目仅存的代表。鸭嘴兽和针鼹在形态和生态学上都非常不同:鸭嘴兽是一种特殊的半水生穴居动物,以淡水无脊椎动物为食,而针鼹则完全是陆生动物,以群居昆虫和蚯蚓为食。有人提出针鼹是从一种半水生的、鸭嘴兽般的祖先进化而来的,但缺乏这种深刻进化转变的化石证据,这一假设仍然存在争议。在这里,我们提供了关于早白垩纪(108 - 103 Ma)澳大利亚哺乳动物Kryoryctes cadburyi的原始数据,目前只从单个肱骨中发现,它提供了与这个问题相关的关键信息。对536个特征的哺乳动物形态矩阵的系统发育分析表明,核细胞是一种茎单目动物。三维整体骨骼对比显示,肱骨的整体形状与针鼹比鸭嘴兽更相似,但微观结构分析揭示了在半水生哺乳动物中发现的特化,包括特别厚的皮质和高度缩小的髓腔,鸭嘴兽中有,而针鼹中没有。证据表明,Kryoryctes是一种半水生穴居动物,表明单孔目动物在中生代首次进化出两栖生活方式,并为单孔目动物作为一个整体的祖先的假设提供了支持。导致现代鸭嘴兽的世系似乎具有极其长期的生态位保守主义特征,针鼹代表了更晚的向完全陆地生活方式的回归。
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 求助全文
来源期刊
CiteScore
19.00
自引率
0.90%
发文量
3575
审稿时长
2.5 months
期刊介绍: The Proceedings of the National Academy of Sciences (PNAS), a peer-reviewed journal of the National Academy of Sciences (NAS), serves as an authoritative source for high-impact, original research across the biological, physical, and social sciences. With a global scope, the journal welcomes submissions from researchers worldwide, making it an inclusive platform for advancing scientific knowledge.
×
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