Bailleul Alida M, O'Connor Jingmai, Schweitzer Mary H
Key Laboratory of Vertebrate Evolution and Human Origins of the Chinese Academy of Sciences, Institute of Vertebrate Paleontology and Paleoanthropology, Beijing, China.
CAS Center for Excellence in Life and Paleoenvironment, Beijing, China.
PeerJ. 2019 Sep 27;7:e7764. doi: 10.7717/peerj.7764. eCollection 2019.
In the mid-19th century, the discovery that bone microstructure in fossils could be preserved with fidelity provided a new avenue for understanding the evolution, function, and physiology of long extinct organisms. This resulted in the establishment of paleohistology as a subdiscipline of vertebrate paleontology, which has contributed greatly to our current understanding of dinosaurs as living organisms. Dinosaurs are part of a larger group of reptiles, the Archosauria, of which there are only two surviving lineages, crocodilians and birds. The goal of this review is to document progress in the field of archosaur paleohistology, focusing in particular on the Dinosauria. We briefly review the "growth age" of dinosaur histology, which has encompassed new and varied directions since its emergence in the 1950s, resulting in a shift in the scientific perception of non-avian dinosaurs from "sluggish" reptiles to fast-growing animals with relatively high metabolic rates. However, fundamental changes in growth occurred within the sister clade Aves, and we discuss this major evolutionary transition as elucidated by histology. We then review recent innovations in the field, demonstrating how paleohistology has changed and expanded to address a diversity of non-growth related questions. For example, dinosaur skull histology has elucidated the formation of curious cranial tissues (e.g., "metaplastic" tissues), and helped to clarify the evolution and function of oral adaptations, such as the dental batteries of duck-billed dinosaurs. Lastly, we discuss the development of novel techniques with which to investigate not only the skeletal tissues of dinosaurs, but also less-studied soft-tissues, through molecular paleontology and paleohistochemistry-recently developed branches of paleohistology-and the future potential of these methods to further explore fossilized tissues. We suggest that the combination of histological and molecular methods holds great potential for examining the preserved tissues of dinosaurs, basal birds, and their extant relatives. This review demonstrates the importance of traditional bone paleohistology, but also highlights the need for innovation and new analytical directions to improve and broaden the utility of paleohistology, in the pursuit of more diverse, highly specific, and sensitive methods with which to further investigate important paleontological questions.
19世纪中叶,化石中骨骼微观结构能够被精确保存这一发现,为理解早已灭绝生物的进化、功能和生理机能提供了一条新途径。这促成了古组织学作为脊椎动物古生物学一个子学科的建立,极大地推动了我们目前将恐龙视为生物的理解。恐龙是爬行动物中一个更大类群——主龙类的一部分,目前主龙类仅存两个谱系,即鳄目和鸟类。本综述的目的是记录主龙类古组织学领域的进展,尤其聚焦恐龙类。我们简要回顾恐龙组织学的“成长年代”,自20世纪50年代出现以来,它涵盖了新的多样方向,导致科学界对非鸟类恐龙的认知从“行动迟缓”的爬行动物转变为生长迅速、代谢率相对较高的动物。然而,在其姊妹类群鸟类中发生了生长方面的根本性变化,我们将讨论组织学所阐明的这一重大进化转变。接着我们回顾该领域最近的创新,展示古组织学如何改变和扩展以解决各种与生长无关的问题。例如,恐龙头骨组织学阐明了奇特颅骨组织(如“化生”组织)的形成,并有助于厘清口腔适应性特征(如鸭嘴恐龙的齿系)的进化和功能。最后,我们讨论新技术的发展,这些技术不仅可用于研究恐龙的骨骼组织,还可通过分子古生物学和古组织化学(古组织学最近发展的分支)研究较少被研究的软组织,以及这些方法进一步探索化石组织的未来潜力。我们认为,组织学和分子方法的结合在研究恐龙、基干鸟类及其现存亲属的保存组织方面具有巨大潜力。本综述展示了传统骨骼古组织学的重要性,但也强调了创新和新分析方向的必要性,以改进和拓宽古组织学的效用,寻求更多样、高度特异和灵敏的方法来进一步研究重要的古生物学问题。