• 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

澳大利亚史前“沼泽之王”:1886年德维斯对上新世—更新世鳄类属的修订。

Australia's prehistoric 'swamp king': revision of the Plio-Pleistocene crocodylian genus de Vis, 1886.

作者信息

Ristevski Jorgo, Yates Adam M, Price Gilbert J, Molnar Ralph E, Weisbecker Vera, Salisbury Steven W

机构信息

School of Biological Sciences, The Univeristy of Queensland, Brisbane, QLD, Australia.

Museum of Central Australia, Museum and Art Gallery of the Northern Territory, Alice Springs, NT, Australia.

出版信息

PeerJ. 2020 Dec 21;8:e10466. doi: 10.7717/peerj.10466. eCollection 2020.

DOI:10.7717/peerj.10466
PMID:33391869
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7759136/
Abstract

The crocodylian fossil record from the Cenozoic of Australasia is notable for its rich taxonomic diversity, and is primarily represented by members of the clade Mekosuchinae. Reports of crocodylian fossils from Australia date back to the late nineteenth century. In 1886, Charles Walter de Vis proposed the name for crocodylian fossils from southeast Queensland-the first binomen given to an extinct crocodylian taxon from Australia. has come to be regarded as a large, broad-snouted crocodylian from Australia's Plio-Pleistocene, and numerous specimens, few of which are sufficiently complete, have been assigned to it by several authors throughout the twentieth century. In the late 1990s, the genus was expanded to include a second species, . Unfortunately, the original syntype series described as is very fragmentary and derives from more than one taxon, while a large part of the subsequently selected lectotype specimen is missing. Because descriptions and illustrations of the complete lectotype do not reveal any autapomorphic features, we propose that should be regarded as a . Following this decision, the fossil material previously referred to is of uncertain taxonomic placement. A partial skull, formerly assigned to and known as 'Geoff Vincent's specimen', possesses many features of diagnostic value and is therefore used as basis to erect a new genus and species gen. et sp. nov. A comprehensive description is given for the osteology of 'Geoff Vincent's specimen' as well as aspects of its palaeoneurology, the latter being a first for an extinct Australian crocodyliform. The newly named genus is characterized by a unique combination of premaxillary features such as a distinctive arching of the anterior alveolar processes of the premaxillae, a peculiar arrangement of the first two premaxillary alveoli and a large size disparity between the 3rd and 4th premaxillary alveoli. These features presently allow formal recognition of two species within the genus, and comb. nov., with the former having comparatively more robust rostral proportions than the latter. The holotype comes from the Pliocene Chinchilla Sand of the Darling Downs, south-eastern Queensland, whereas the material assigned to is from the Pleistocene of Terrace Site Local Fauna, Riversleigh, northwest Queensland. Phylogenetic analyses recover as a mekosuchine, although further cladistic assessments are needed to better understand the relationships within the clade.

摘要

澳大拉西亚新生代的鳄鱼化石记录以其丰富的分类多样性而闻名,主要由麦氏鳄亚科的成员代表。澳大利亚鳄鱼化石的报告可追溯到19世纪末。1886年,查尔斯·沃尔特·德·维斯为昆士兰东南部的鳄鱼化石命名,这是给澳大利亚已灭绝鳄鱼分类单元的第一个双名法名称。后来被认为是来自澳大利亚上新世 - 更新世的一种大型宽吻鳄鱼,在整个20世纪,许多作者将众多标本(其中很少有足够完整的)归入该属。在20世纪90年代后期,该属被扩大到包括第二个物种。不幸的是,最初描述为的模式系列非常破碎,且来自不止一个分类单元,而随后选定的主模式标本的很大一部分缺失了。由于完整主模式标本的描述和图示未揭示任何自近裔性状特征,我们提议应将视为一个。基于这一决定,先前归入的化石材料的分类位置不确定。一个部分头骨,以前归入并被称为“杰夫·文森特标本”,具有许多诊断价值的特征,因此被用作建立一个新属和新物种的基础。对“杰夫·文森特标本”的骨骼学以及古神经学方面进行了全面描述(后者是对已灭绝澳大利亚鳄形类动物的首次描述)。新命名的属的特征是上颌骨特征的独特组合,如下颌前齿槽突的独特拱形、前两个上颌齿槽的特殊排列以及第三和第四上颌齿槽之间较大的尺寸差异。目前,这些特征使得该属内能够正式识别出两个物种,和新组合,前者的吻部比例相对比后者更粗壮。的正模标本来自昆士兰东南部达令唐斯的上新世钦奇拉砂岩,而归入的材料来自昆士兰西北部里弗斯利阶地遗址地方动物群的更新世。系统发育分析将恢复为麦氏鳄类,尽管需要进一步的分支系统评估来更好地理解该类群内部的关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/685c081b8921/peerj-08-10466-g039.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/959b7f95cbd2/peerj-08-10466-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/61d459a335f0/peerj-08-10466-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/08b187bf5e3b/peerj-08-10466-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/a7f6a5f6829e/peerj-08-10466-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/cbd03c5854cb/peerj-08-10466-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/4bfdc8852b2a/peerj-08-10466-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/3ddb69519af1/peerj-08-10466-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/2721f948d0ba/peerj-08-10466-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/a58e88ffb4fd/peerj-08-10466-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/a61b30f565cb/peerj-08-10466-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/5bf94d3f1b9d/peerj-08-10466-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/28aa9a7306b5/peerj-08-10466-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/c09dc32dc8f4/peerj-08-10466-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/11a6f6f7f173/peerj-08-10466-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/42fec0bfa866/peerj-08-10466-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/38ea34179002/peerj-08-10466-g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/9aa07443ddde/peerj-08-10466-g018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/d08d44709e18/peerj-08-10466-g019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/c08ed57f0389/peerj-08-10466-g020.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/0e33acff7d90/peerj-08-10466-g021.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/b8776e431993/peerj-08-10466-g022.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/40cb605d61ac/peerj-08-10466-g023.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/1ca877f8fc3c/peerj-08-10466-g024.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/114cc3212e5a/peerj-08-10466-g025.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/f3a814be33f9/peerj-08-10466-g026.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/7cd606097931/peerj-08-10466-g027.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/7141dfa3b1a5/peerj-08-10466-g028.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/67b7083da785/peerj-08-10466-g029.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/3a7b79f36aee/peerj-08-10466-g030.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/a07948bd949b/peerj-08-10466-g031.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/efd9052c6ca8/peerj-08-10466-g032.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/eaa126168751/peerj-08-10466-g033.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/ddfdf689aff5/peerj-08-10466-g034.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/d27bb19c7975/peerj-08-10466-g035.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/5bcaee67b087/peerj-08-10466-g036.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/5a9a3d9f1e21/peerj-08-10466-g037.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/4395d59e8d48/peerj-08-10466-g038.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/685c081b8921/peerj-08-10466-g039.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/959b7f95cbd2/peerj-08-10466-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/61d459a335f0/peerj-08-10466-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/08b187bf5e3b/peerj-08-10466-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/a7f6a5f6829e/peerj-08-10466-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/cbd03c5854cb/peerj-08-10466-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/4bfdc8852b2a/peerj-08-10466-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/3ddb69519af1/peerj-08-10466-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/2721f948d0ba/peerj-08-10466-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/a58e88ffb4fd/peerj-08-10466-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/a61b30f565cb/peerj-08-10466-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/5bf94d3f1b9d/peerj-08-10466-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/28aa9a7306b5/peerj-08-10466-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/c09dc32dc8f4/peerj-08-10466-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/11a6f6f7f173/peerj-08-10466-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/42fec0bfa866/peerj-08-10466-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/38ea34179002/peerj-08-10466-g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/9aa07443ddde/peerj-08-10466-g018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/d08d44709e18/peerj-08-10466-g019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/c08ed57f0389/peerj-08-10466-g020.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/0e33acff7d90/peerj-08-10466-g021.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/b8776e431993/peerj-08-10466-g022.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/40cb605d61ac/peerj-08-10466-g023.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/1ca877f8fc3c/peerj-08-10466-g024.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/114cc3212e5a/peerj-08-10466-g025.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/f3a814be33f9/peerj-08-10466-g026.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/7cd606097931/peerj-08-10466-g027.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/7141dfa3b1a5/peerj-08-10466-g028.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/67b7083da785/peerj-08-10466-g029.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/3a7b79f36aee/peerj-08-10466-g030.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/a07948bd949b/peerj-08-10466-g031.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/efd9052c6ca8/peerj-08-10466-g032.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/eaa126168751/peerj-08-10466-g033.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/ddfdf689aff5/peerj-08-10466-g034.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/d27bb19c7975/peerj-08-10466-g035.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/5bcaee67b087/peerj-08-10466-g036.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/5a9a3d9f1e21/peerj-08-10466-g037.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/4395d59e8d48/peerj-08-10466-g038.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45eb/7759136/685c081b8921/peerj-08-10466-g039.jpg

相似文献

1
Australia's prehistoric 'swamp king': revision of the Plio-Pleistocene crocodylian genus de Vis, 1886.澳大利亚史前“沼泽之王”:1886年德维斯对上新世—更新世鳄类属的修订。
PeerJ. 2020 Dec 21;8:e10466. doi: 10.7717/peerj.10466. eCollection 2020.
2
First record of a tomistomine crocodylian from Australia.首次在澳大利亚记录到长吻鳄科鳄形目动物。
Sci Rep. 2021 Jun 9;11(1):12158. doi: 10.1038/s41598-021-91717-y.
3
Cranial anatomy of the mekosuchine crocodylian Trilophosuchus rackhami Willis, 1993.美索不达米亚鳄形超目动物瑞钦鳄的颅部解剖结构。
Anat Rec (Hoboken). 2023 Feb;306(2):239-297. doi: 10.1002/ar.25050. Epub 2022 Aug 29.
4
A new look at an old Australian raptor places Taphaetus lacertosus de Vis 1905 in the Old World vultures (Accipitridae: Aegypiinae).重新审视澳大利亚古老的猛禽,将 Taphaetus lacertosus de Vis 1905 归入旧大陆秃鹫(鹰科:Aegypiinae)。
Zootaxa. 2022 Jul 20;5168(1):1-23. doi: 10.11646/zootaxa.5168.1.1.
5
Taxonomic review of two fossil crocodylians from the Cenozoic of South America and its implications for the crocodylian fauna of the continent.对来自南美洲新生代的两种化石鳄类的分类学综述及其对该大陆鳄类动物群的意义。
Zootaxa. 2019 Aug 14;4656(3):zootaxa.4656.3.5. doi: 10.11646/zootaxa.4656.3.5.
6
Neuroanatomy of the mekosuchine crocodylian Trilophosuchus rackhami Willis, 1993.美索不达米亚鳄形超目鳄科的梅克索鳄属 Trilophosuchus rackhami Willis, 1993 的神经解剖学。
J Anat. 2022 Oct;241(4):981-1013. doi: 10.1111/joa.13732. Epub 2022 Aug 29.
7
The Luciolinae of S. E. Asia and the Australopacific region: a revisionary checklist (Coleoptera: Lampyridae) including description of three new genera and 13 new species.东南亚及澳大拉西亚-太平洋地区的光萤亚科:一份修订名录(鞘翅目:萤科),包括三个新属及13个新种的描述
Zootaxa. 2019 Oct 18;4687(1):zootaxa.4687.1.1. doi: 10.11646/zootaxa.4687.1.1.
8
Hydroids (Cnidaria, Hydrozoa) from Mauritanian Coral Mounds.来自毛里塔尼亚珊瑚丘的水螅虫纲动物(刺胞动物门,水螅虫纲)。
Zootaxa. 2020 Nov 16;4878(3):zootaxa.4878.3.2. doi: 10.11646/zootaxa.4878.3.2.
9
The biochronology and palaeobiogeography of (Crocodylia: Mekosuchinae) based on new specimens from the Northern Territory and Queensland, Australia.基于澳大利亚北领地和昆士兰新标本的(鳄目:麦氏鳄亚科)生物年代学与古生物地理学研究
PeerJ. 2017 Jun 21;5:e3458. doi: 10.7717/peerj.3458. eCollection 2017.
10
A new horned crocodile from the Plio-Pleistocene hominid sites at Olduvai Gorge, Tanzania.来自坦桑尼亚奥杜威峡谷上新世至更新世人类遗址的一种新角鳄。
PLoS One. 2010 Feb 24;5(2):e9333. doi: 10.1371/journal.pone.0009333.

引用本文的文献

1
A new Crocodyloidea from the middle Eocene of Zamora (Duero Basin, Spain).来自西班牙杜罗盆地萨莫拉中始新世的一种新鳄形超目动物。
Anat Rec (Hoboken). 2025 Jun;308(6):1692-1706. doi: 10.1002/ar.25422. Epub 2024 Mar 5.
2
Neuroanatomy of the crocodylian Tomistoma dowsoni from the Miocene of North Africa provides insights into the evolutionary history of gavialoids.北非中新世的鳄形超目动物多索托玛化石的神经解剖结构为探讨长吻鳄类的进化历史提供了线索。
J Anat. 2023 Jul;243(1):1-22. doi: 10.1111/joa.13846. Epub 2023 Mar 16.
3
Neuroanatomy of the crocodylomorph Portugalosuchus azenhae from the late cretaceous of Portugal.

本文引用的文献

1
THE RETENTION INDEX AND THE RESCALED CONSISTENCY INDEX.保留指数与重新标度的一致性指数。
Cladistics. 1989 Dec;5(4):417-419. doi: 10.1111/j.1096-0031.1989.tb00573.x.
2
ESTIMATING CHARACTER WEIGHTS DURING TREE SEARCH.在树搜索过程中估计字符权重。
Cladistics. 1993 Mar;9(1):83-91. doi: 10.1111/j.1096-0031.1993.tb00209.x.
3
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。
葡萄牙晚白垩世鳄形超目葡萄牙蛮鳄的神经解剖学。
J Anat. 2023 Jun;242(6):1146-1171. doi: 10.1111/joa.13836. Epub 2023 Feb 2.
4
Cranial anatomy of the mekosuchine crocodylian Trilophosuchus rackhami Willis, 1993.美索不达米亚鳄形超目动物瑞钦鳄的颅部解剖结构。
Anat Rec (Hoboken). 2023 Feb;306(2):239-297. doi: 10.1002/ar.25050. Epub 2022 Aug 29.
5
Neuroanatomy of the mekosuchine crocodylian Trilophosuchus rackhami Willis, 1993.美索不达米亚鳄形超目鳄科的梅克索鳄属 Trilophosuchus rackhami Willis, 1993 的神经解剖学。
J Anat. 2022 Oct;241(4):981-1013. doi: 10.1111/joa.13732. Epub 2022 Aug 29.
6
An intermediate crocodylian linking two extant gharials from the Bronze Age of China and its human-induced extinction.一种中间鳄类,将中国青铜时代的两种现存长吻鳄联系起来,以及它们因人类而灭绝。
Proc Biol Sci. 2022 Mar 9;289(1970):20220085. doi: 10.1098/rspb.2022.0085.
7
The impact of molecular data on the phylogenetic position of the putative oldest crown crocodilian and the age of the clade.分子数据对假定最古老的冠鳄类的系统发育位置和进化枝的年龄的影响。
Biol Lett. 2022 Feb;18(2):20210603. doi: 10.1098/rsbl.2021.0603. Epub 2022 Feb 9.
8
Phylogenetic analysis of a new morphological dataset elucidates the evolutionary history of Crocodylia and resolves the long-standing gharial problem.一项新形态数据集的系统发育分析阐明了鳄目动物的进化史,并解决了长期存在的印度食鱼鳄问题。
PeerJ. 2021 Sep 6;9:e12094. doi: 10.7717/peerj.12094. eCollection 2021.
9
A diverse Late Cretaceous vertebrate tracksite from the Winton Formation of Queensland, Australia.来自澳大利亚昆士兰州温顿组的一个多样的晚白垩世脊椎动物足迹化石点。
PeerJ. 2021 Jun 17;9:e11544. doi: 10.7717/peerj.11544. eCollection 2021.
10
First record of a tomistomine crocodylian from Australia.首次在澳大利亚记录到长吻鳄科鳄形目动物。
Sci Rep. 2021 Jun 9;11(1):12158. doi: 10.1038/s41598-021-91717-y.
Cladistics. 2016 Jun;32(3):221-238. doi: 10.1111/cla.12160. Epub 2016 Apr 25.
4
Weighted parsimony outperforms other methods of phylogenetic inference under models appropriate for morphology.在适用于形态学的模型下,加权简约法比其他系统发育推断方法表现更优。
Cladistics. 2018 Aug;34(4):407-437. doi: 10.1111/cla.12205. Epub 2017 Jun 4.
5
Mosaic nature in the skeleton of East Asian crocodylians fills the morphological gap between "Tomistominae" and Gavialinae.东亚鳄类骨骼的镶嵌特征填补了“切喙鳄亚科”和食鱼鳄亚科之间的形态学空白。
Cladistics. 2019 Dec;35(6):623-632. doi: 10.1111/cla.12372. Epub 2019 Jan 20.
6
Extinction of eastern Sahul megafauna coincides with sustained environmental deterioration.东亚澳大拉西亚巨型动物群的灭绝与持续的环境恶化相一致。
Nat Commun. 2020 May 18;11(1):2250. doi: 10.1038/s41467-020-15785-w.
7
The Frontoparietal Fossa and Dorsotemporal Fenestra of Archosaurs and Their Significance for Interpretations of Vascular and Muscular Anatomy in Dinosaurs.兽脚亚目恐龙的额顶窝和背颞窗及其对恐龙血管和肌肉解剖结构解释的意义。
Anat Rec (Hoboken). 2020 Apr;303(4):1060-1074. doi: 10.1002/ar.24218. Epub 2019 Jul 13.
8
Quantitative heterodonty in Crocodylia: assessing size and shape across modern and extinct taxa.鳄目动物的定量异形:评估现代和已灭绝类群的大小和形状
PeerJ. 2019 Feb 28;7:e6485. doi: 10.7717/peerj.6485. eCollection 2019.
9
A new phylogenetic analysis of Phytosauria (Archosauria: Pseudosuchia) with the application of continuous and geometric morphometric character coding.一项运用连续和几何形态测量特征编码对植龙目(主龙形下纲:伪鳄类)进行的新系统发育分析。
PeerJ. 2018 Dec 10;6:e5901. doi: 10.7717/peerj.5901. eCollection 2018.
10
On the median pharyngeal valve of the American alligator (Alligator mississippiensis).关于美国短吻鳄(密西西比鳄)的咽中瓣。
J Morphol. 2019 Jan;280(1):58-67. doi: 10.1002/jmor.20914. Epub 2018 Dec 5.