三叶虫的发育。

IF 11 1区 生物学 Q1 BIOLOGY
Tao Dai, Xingliang Zhang
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引用次数: 0

摘要

本文全面回顾了近几十年来从寒武纪第 2 系和第 3 系地层中发现的三叶虫的完整发育序列。这些标本大多为铰接式标本,形态细腻,甚至保存了不同生长阶段的精细结构,如喙囊、轴孔、棘孔、鳃缘棘和线状共栖结构。它们的躯干分节时间表显示了一致的分节生成和释放发育模式,即在每次蜕皮之后异时发生标记形成和体节形成,这为等体甚至巨体三叶虫的潜在发育策略提供了线索。由于胸节的形成速度明显超过衔接速度,因此胸节的形成过程看似漫长,这或许可以解释为什么蜕皮三叶虫的胸节数量固定而有限。此外,入学机制与躯干分节之间的关系证实了三叶虫中这种极为不寻常的生长模式,揭示了这些早期分化的三叶虫在其生命周期中控制分节增加和释放速度的原因,因此对节肢动物身体形态的进化具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of eodiscinid trilobites.

A comprehensive review of a full developmental sequence of eodiscinid trilobites reported in recent decades from Cambrian Series 2 and 3 strata is presented. These mostly articulated specimens exhibit detailed morphologies with preservation of even delicate structures at different growth stages, such as the bacculae, axial pores, spine pores, pygidial marginal spines and line coaptative structures. Their trunk segmentation schedules displayed a consistent developmental mode in segment generation and liberation, that is tagmosis and somitogenesis occurred heterochronously after each moulting event, providing clues regarding the potential developmental strategy in isopygous and even macropygous trilobites. The fact that the rate of segmentation obviously exceeds that of articulation results in a seemingly prolonged process of the formation of thoracic segments, which might explain why eodiscinid trilobites have a fixed and limited number of thoracic segments. In addition, the relationship between enrollment mechanism and trunk segmentation during eodiscinid ontogeny confirms this highly unusual growth pattern among the Trilobita, revealing why these early-diverging trilobites controlled the rate of segment increase and release during their life cycles, and is thus of interest with regard to the evolution of arthropod body patterning.

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来源期刊
Biological Reviews
Biological Reviews 生物-生物学
CiteScore
21.30
自引率
2.00%
发文量
99
审稿时长
6-12 weeks
期刊介绍: Biological Reviews is a scientific journal that covers a wide range of topics in the biological sciences. It publishes several review articles per issue, which are aimed at both non-specialist biologists and researchers in the field. The articles are scholarly and include extensive bibliographies. Authors are instructed to be aware of the diverse readership and write their articles accordingly. The reviews in Biological Reviews serve as comprehensive introductions to specific fields, presenting the current state of the art and highlighting gaps in knowledge. Each article can be up to 20,000 words long and includes an abstract, a thorough introduction, and a statement of conclusions. The journal focuses on publishing synthetic reviews, which are based on existing literature and address important biological questions. These reviews are interesting to a broad readership and are timely, often related to fast-moving fields or new discoveries. A key aspect of a synthetic review is that it goes beyond simply compiling information and instead analyzes the collected data to create a new theoretical or conceptual framework that can significantly impact the field. Biological Reviews is abstracted and indexed in various databases, including Abstracts on Hygiene & Communicable Diseases, Academic Search, AgBiotech News & Information, AgBiotechNet, AGRICOLA Database, GeoRef, Global Health, SCOPUS, Weed Abstracts, and Reaction Citation Index, among others.
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