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IF 2.3 4区 医学 Q3 NEUROSCIENCES
Jared T. Voris, François Therrien, Ryan C. Ridgely, Lawrence M. Witmer, Darla K. Zelenitsky
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引用次数: 0

摘要

在过去的二十年中,计算机断层扫描(CT)的普及极大地促进了对许多已灭绝兽脚亚目类群的颅内记录。然而,这些研究大多集中在成熟个体的形态学上,因此兽脚亚目动物通过个体发生的颅内变化或变异在很大程度上仍然未知。目前的研究在个体发生和进化的背景下,揭示了准暴龙类暴龙——libratus Gorgosaurus的颅内解剖结构。基于CT扫描的6个Gorgosaurus脑瘤,包括最近发现的两个幼年个体,我们虚拟地重建和描述了一个生长系列的颅内形态。尽管颅骨结构发生了相当大的变化,但在Gorgosaurus的颅腔内发生的个体发生变化相对较少。这些变化包括与青少年相比,成人内胆后脑区长度的细微增加和鼓室憩室肿胀的增加。其中最显著的个体发生变化是随着gogosaurus的成熟,颅腔内脑形态的独特性降低。幼兽龙的脑内模比更大、更成熟的个体表现出更清晰的大脑半球、视叶和小脑。这表明幼年暴龙的内胆和大脑之间有更密切的对应关系,表明幼年个体的内胆比成熟个体的内胆更准确地反映了大脑的结构及其区域。的大脑Gorgosaurus显示基底archosaurian特征和更多的衍生形态特征。更原始的始祖龙脑特征包括较大的嗅球和嗅束,脑的后腹长轴,以及位于脑后的视叶,而衍生特征包括明显的后脑弯曲,稍大的大脑,以及至少部分分离左右视叶的小脑。通过对早期分化的兽脚亚目动物(如异龙亚目、巨龙亚目和腔骨亚目)的幼年个体(更能反映不同大脑区域的结构/组织)的研究,可以进一步阐明这些衍生特征的进化获得过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ontogenetic Changes in Endocranial Anatomy in Gorgosaurus libratus (Theropoda: Tyrannosauridae) Provide Insight Into the Evolution of the Tyrannosauroid Endocranium

Ontogenetic Changes in Endocranial Anatomy in Gorgosaurus libratus (Theropoda: Tyrannosauridae) Provide Insight Into the Evolution of the Tyrannosauroid Endocranium

Over the past two decades, increased accessibility to computed tomography (CT) scanners has greatly facilitated documentation of the endocranium in numerous extinct theropod taxa. However, most of these studies have focused on the morphology of mature individuals, thus changes or variation through ontogeny of the endocranium in theropods remains largely unknown. The current study sheds light on the endocranial anatomy of the eutyrannosaurian tyrannosauroid, Gorgosaurus libratus, in both an ontogenetic and evolutionary context. Based on CT scans of six Gorgosaurus braincases, including those of two recently discovered juvenile individuals, we virtually reconstruct and describe the endocranial morphology for a growth series of G. libratus. Despite considerable changes in skull architecture, relatively few ontogenetic changes occurred in the endocranium of Gorgosaurus. These changes include a subtle increase in the length of the hindbrain region of the endocast and increased inflation of the tympanic sinus diverticula in adults relative to juveniles. Among the most significant ontogenetic changes is a decrease in the distinctiveness of the brain morphology in endocasts as Gorgosaurus mature. The endocasts of juvenile Gorgosaurus exhibit better defined cerebral hemispheres, optic lobes, and cerebella than those of larger and more mature individuals. This suggests a closer correspondence between the endocast and the brain in juvenile tyrannosaurids, indicating the endocast of juvenile individuals provides a more accurate representation of the structure of the brain and its regions relative to the endocast of more mature individuals. The brain of Gorgosaurus displays a mix of basal archosaurian traits and more derived coelurosaurian traits. More primitive archosaurian features of the Gorgosaurus brain include large olfactory bulbs and tracts, a posteroventrally oriented long axis of the cerebrum, and posteriorly positioned optic lobes, whereas derived features include prominent hindbrain flexure, a somewhat enlarged cerebrum, and a cerebellum that at least partially separates the left and right optic lobes. An understanding of the evolutionary acquisition of such derived features leading to the avian brain may be further elucidated via the study of the endocasts of juvenile individuals (more reflective of the structure/organization of various brain regions) of earlier-diverging theropods (e.g., Allosauroidea, Megalosauroidea, and Coelophysoidea).

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来源期刊
CiteScore
5.80
自引率
8.00%
发文量
158
审稿时长
3-6 weeks
期刊介绍: Established in 1891, JCN is the oldest continually published basic neuroscience journal. Historically, as the name suggests, the journal focused on a comparison among species to uncover the intricacies of how the brain functions. In modern times, this research is called systems neuroscience where animal models are used to mimic core cognitive processes with the ultimate goal of understanding neural circuits and connections that give rise to behavioral patterns and different neural states. Research published in JCN covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of nervous systems in species with an emphasis on the way that species adaptations inform about the function or organization of the nervous systems, rather than on their evolution per se. JCN publishes primary research articles and critical commentaries and review-type articles offering expert insight in to cutting edge research in the field of systems neuroscience; a complete list of contribution types is given in the Author Guidelines. For primary research contributions, only full-length investigative reports are desired; the journal does not accept short communications.
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