• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

安哥拉本提巴山的喙头目薄板龙科鱼龙 Cardiocorax mukulu 的颅部解剖结构和关系。

The cranial anatomy and relationships of Cardiocorax mukulu (Plesiosauria: Elasmosauridae) from Bentiaba, Angola.

机构信息

Huffington Department of Earth Sciences, ISEM at Southern Methodist University, Dallas, Texas, United States of America.

GeoBioTec + Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, Caparica, Portugal.

出版信息

PLoS One. 2021 Aug 17;16(8):e0255773. doi: 10.1371/journal.pone.0255773. eCollection 2021.

DOI:10.1371/journal.pone.0255773
PMID:34403433
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8370651/
Abstract

We report a new specimen of the plesiosaur Cardiocorax mukulu that includes the most complete plesiosaur skull from sub-Saharan Africa. The well-preserved three-dimensional nature of the skull offers rare insight into the cranial anatomy of elasmosaurid plesiosaurians. The new specimen of Cardiocorax mukulu was recovered from Bentiaba, Namibe Province in Angola, approximately three meters above the holotype. The new specimen also includes an atlas-axis complex, seventeen postaxial cervical vertebrae, partial ribs, a femur, and limb elements. It is identified as Cardiocorax mukulu based on an apomorphy shared with the holotype where the cervical neural spine is approximately as long anteroposteriorly as the centrum and exhibits a sinusoidal anterior margin. The new specimen is nearly identical to the holotype and previously referred material in all other aspects. Cardiocorax mukulu is returned in an early-branching or intermediate position in Elasmosauridae in four out of the six of our phylogenetic analyses. Cardiocorax mukulu lacks the elongated cervical vertebrae that is characteristic of the extremely long-necked elasmosaurines, and the broad skull with and a high number of maxillary teeth (28-40) which is characteristic of Aristonectinae. Currently, the most parsimonious explanation concerning elasmosaurid evolutionary relationships, is that Cardiocorax mukulu represents an older lineage of elasmosaurids in the Maastrichtian.

摘要

我们报告了一个新的上龙标本,Cardiocorax mukulu,它包括来自撒哈拉以南非洲最完整的上龙头骨。头骨保存完好的三维性质为了解海龙类上龙的颅解剖结构提供了难得的见解。新的 Cardiocorax mukulu 标本来自安哥拉纳米贝省的本蒂瓦巴,位于正型标本上方约三米处。新标本还包括一个寰枢椎复合体、十七个轴后颈椎、部分肋骨、股骨和肢骨元素。它被鉴定为 Cardiocorax mukulu,基于与正型标本共享的一个特征,即颈椎神经棘前后长约与中心体相同,并具有正弦形前缘。新标本在所有其他方面都与正型标本和以前归入的材料几乎相同。在我们的六个系统发育分析中的四个分析中,Cardiocorax mukulu 在海龙科中处于早期分支或中间位置。Cardiocorax mukulu 缺乏极度长颈的海龙类所特有的长颈椎,以及宽头骨和高数量的上颌齿(28-40 颗),这是 Aristonectinae 的特征。目前,关于海龙类进化关系的最简约解释是,Cardiocorax mukulu 代表了马斯特里赫特阶海龙类的一个更早的谱系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/aeba76029ecd/pone.0255773.g026.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/ac029401778e/pone.0255773.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/a63666774039/pone.0255773.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/558b56c0da70/pone.0255773.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/bae91e433a4d/pone.0255773.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/b6093ffe8efb/pone.0255773.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/f2f8c8e49e85/pone.0255773.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/7a69aedd805e/pone.0255773.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/9127d85a4578/pone.0255773.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/f7788bdcf48d/pone.0255773.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/2c7ead994957/pone.0255773.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/1b7651b058e4/pone.0255773.g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/fc31a316eef5/pone.0255773.g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/eff0c66a8a08/pone.0255773.g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/920fd931e4c8/pone.0255773.g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/e214f9c419f5/pone.0255773.g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/671b4c02e565/pone.0255773.g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/e2761bd79619/pone.0255773.g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/15fd2cbe26bc/pone.0255773.g018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/947e8263c857/pone.0255773.g019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/d297b034d6ac/pone.0255773.g020.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/ff9dfb3ffab5/pone.0255773.g021.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/cfdb6445a5b7/pone.0255773.g022.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/e7457c4aafd4/pone.0255773.g023.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/5b1ee3b37a6d/pone.0255773.g024.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/b8f58ea67fc0/pone.0255773.g025.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/aeba76029ecd/pone.0255773.g026.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/ac029401778e/pone.0255773.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/a63666774039/pone.0255773.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/558b56c0da70/pone.0255773.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/bae91e433a4d/pone.0255773.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/b6093ffe8efb/pone.0255773.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/f2f8c8e49e85/pone.0255773.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/7a69aedd805e/pone.0255773.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/9127d85a4578/pone.0255773.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/f7788bdcf48d/pone.0255773.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/2c7ead994957/pone.0255773.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/1b7651b058e4/pone.0255773.g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/fc31a316eef5/pone.0255773.g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/eff0c66a8a08/pone.0255773.g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/920fd931e4c8/pone.0255773.g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/e214f9c419f5/pone.0255773.g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/671b4c02e565/pone.0255773.g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/e2761bd79619/pone.0255773.g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/15fd2cbe26bc/pone.0255773.g018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/947e8263c857/pone.0255773.g019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/d297b034d6ac/pone.0255773.g020.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/ff9dfb3ffab5/pone.0255773.g021.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/cfdb6445a5b7/pone.0255773.g022.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/e7457c4aafd4/pone.0255773.g023.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/5b1ee3b37a6d/pone.0255773.g024.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/b8f58ea67fc0/pone.0255773.g025.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4723/8370651/aeba76029ecd/pone.0255773.g026.jpg

相似文献

1
The cranial anatomy and relationships of Cardiocorax mukulu (Plesiosauria: Elasmosauridae) from Bentiaba, Angola.安哥拉本提巴山的喙头目薄板龙科鱼龙 Cardiocorax mukulu 的颅部解剖结构和关系。
PLoS One. 2021 Aug 17;16(8):e0255773. doi: 10.1371/journal.pone.0255773. eCollection 2021.
2
Revised vertebral count in the "longest-necked vertebrate" Elasmosaurus platyurus Cope 1868, and clarification of the cervical-dorsal transition in Plesiosauria.修订后的“最长颈脊椎动物”扁鳍龙(Elasmosaurus platyurus Cope 1868)的椎体数,以及对蛇颈龙类颈椎-背椎过渡的澄清。
PLoS One. 2013 Aug 5;8(8):e70877. doi: 10.1371/journal.pone.0070877. Print 2013.
3
Head size, weaponry, and cervical adaptation: Testing craniocervical evolutionary hypotheses in Ceratopsia.头部大小、武器装备与颈椎适应性:在角龙类中检验颅颈进化假说
Evolution. 2015 Jul;69(7):1728-44. doi: 10.1111/evo.12693. Epub 2015 Jul 14.
4
A Basal Lithostrotian Titanosaur (Dinosauria: Sauropoda) with a Complete Skull: Implications for the Evolution and Paleobiology of Titanosauria.一种具有完整头骨的基础锂盐龙类泰坦巨龙(恐龙纲:蜥脚亚目):对泰坦巨龙类演化和古生物学的启示
PLoS One. 2016 Apr 26;11(4):e0151661. doi: 10.1371/journal.pone.0151661. eCollection 2016.
5
Aquatic Habits and Niche Partitioning in the Extraordinarily Long-Necked Triassic Reptile Tanystropheus.三叠纪超长颈爬行动物谭氏鱼的水生习性和生态位分化。
Curr Biol. 2020 Oct 5;30(19):3889-3895.e2. doi: 10.1016/j.cub.2020.07.025. Epub 2020 Aug 6.
6
Lindwurmia, a new genus of Plesiosauria (Reptilia: Sauropterygia) from the earliest Jurassic of Halberstadt, northwest Germany.林德龙属,一种来自德国西北部哈尔伯施塔特早侏罗世的新的蛇颈龙属(爬行纲:鳍龙超目)。
Naturwissenschaften. 2019 Jan 28;106(1-2):5. doi: 10.1007/s00114-018-1600-y.
7
A new basal ornithopod (Dinosauria: Ornithischia) from the Early Cretaceous of Texas.来自德克萨斯州早白垩世的一新基干鸟脚类恐龙(恐龙纲:鸟臀目)。
PLoS One. 2019 Mar 12;14(3):e0207935. doi: 10.1371/journal.pone.0207935. eCollection 2019.
8
The elongated neck of sauropodomorph dinosaurs evolved gradually.蜥脚形亚目恐龙的长颈是逐渐演化而来的。
Anat Rec (Hoboken). 2024 Apr;307(4):1060-1070. doi: 10.1002/ar.25107. Epub 2022 Oct 26.
9
The osteology of the basal archosauromorph Tasmaniosaurus triassicus from the Lower Triassic of Tasmania, Australia.来自澳大利亚塔斯马尼亚下三叠统的基础主龙形类三叠塔斯马尼亚龙的骨骼学。
PLoS One. 2014 Jan 30;9(1):e86864. doi: 10.1371/journal.pone.0086864. eCollection 2014.
10
A new elasmosaurid (Sauropterygia: Plesiosauria) from the non-marine to paralic Dinosaur Park Formation of southern Alberta, Canada.来自加拿大艾伯塔省南部非海相至近海的恐龙公园组的一种新的薄板龙科(蜥鳍目:蛇颈龙目)动物。
PeerJ. 2021 Feb 11;9:e10720. doi: 10.7717/peerj.10720. eCollection 2021.

本文引用的文献

1
TNT version 1.5, including a full implementation of phylogenetic morphometrics.TNT版本1.5,包括系统发育形态计量学的完整实现。
Cladistics. 2016 Jun;32(3):221-238. doi: 10.1111/cla.12160. Epub 2016 Apr 25.
2
A new elasmosaurid (Sauropterygia: Plesiosauria) from the non-marine to paralic Dinosaur Park Formation of southern Alberta, Canada.来自加拿大艾伯塔省南部非海相至近海的恐龙公园组的一种新的薄板龙科(蜥鳍目:蛇颈龙目)动物。
PeerJ. 2021 Feb 11;9:e10720. doi: 10.7717/peerj.10720. eCollection 2021.
3
Estimating the evolutionary rates in mosasauroids and plesiosaurs: discussion of niche occupation in Late Cretaceous seas.
沧龙类和蛇颈龙类的进化速率估算:关于白垩纪晚期海洋生态位占据的讨论
PeerJ. 2020 Apr 13;8:e8941. doi: 10.7717/peerj.8941. eCollection 2020.
4
Synchrotron microtomography of a Nothosaurus marchicus skull informs on nothosaurian physiology and neurosensory adaptations in early Sauropterygia.马尔基诺托龙(Nothosaurus marchicus)头骨的同步加速器显微断层扫描揭示了早期鳍龙超目动物的生理特征和神经感觉适应性。
PLoS One. 2018 Jan 3;13(1):e0188509. doi: 10.1371/journal.pone.0188509. eCollection 2018.
5
A Triassic plesiosaurian skeleton and bone histology inform on evolution of a unique body plan.三叠纪蛇颈龙骨架和骨组织学为独特身体结构的演化提供了信息。
Sci Adv. 2017 Dec 13;3(12):e1701144. doi: 10.1126/sciadv.1701144. eCollection 2017 Dec.
6
Evolution of the Sauropterygian Labyrinth with Increasingly Pelagic Lifestyles.具有日益海洋生活方式的蜥脚形亚目动物的耳室演化。
Curr Biol. 2017 Dec 18;27(24):3852-3858.e3. doi: 10.1016/j.cub.2017.10.069. Epub 2017 Dec 7.
7
Reappraisal of Europe's most complete Early Cretaceous plesiosaurian: Wegner, 1914 from the "Wealden facies" of Germany.对欧洲最完整的早白垩世蛇颈龙的重新评估:1914年韦格纳所描述的来自德国“威尔德相”的标本
PeerJ. 2016 Dec 22;4:e2813. doi: 10.7717/peerj.2813. eCollection 2016.
8
Taxonomic reassessment of Hydralmosaurus as Styxosaurus: new insights on the elasmosaurid neck evolution throughout the Cretaceous.对作为冥河龙的海王龙进行分类重新评估:关于整个白垩纪薄板龙科颈部演化的新见解。
PeerJ. 2016 Mar 15;4:e1777. doi: 10.7717/peerj.1777. eCollection 2016.
9
Faunal turnover of marine tetrapods during the Jurassic-Cretaceous transition.海洋四足动物在侏罗纪-白垩纪过渡期的动物地理区系变化。
Biol Rev Camb Philos Soc. 2014 Feb;89(1):1-23. doi: 10.1111/brv.12038. Epub 2013 Apr 13.
10
Anatomy of the fully formed chondrocranium of Emydura subglobosa (Chelidae): a pleurodiran turtle.亚圆澳龟(蛇颈龟科)完全发育的软骨颅解剖结构:一种侧颈龟。
J Morphol. 2013 Jan;274(1):1-10. doi: 10.1002/jmor.20070. Epub 2012 Sep 13.