个体发育相关性,而非直接适应性,可解释镫骨形态的演变

IF 8.3 1区 生物学 Q1 PLANT SCIENCES
New Phytologist Pub Date : 2024-10-26 DOI:10.1111/nph.20185
Jacob S. Suissa, Karl J. Niklas, Alexandru M. F. Tomescu, William E. Friedman
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引用次数: 0

摘要

摘要近两个世纪以来,植物的初级维管系统(骨架)一直吸引着古植物学家、发育生物学家、系统学家和生理学家的兴趣。蕨类植物具有多样的支柱形态、深厚的进化历史和突出的化石记录,一直是支柱研究的重点。为了解释支柱形态的多样性,过去的适应性假说将生物力学、水力学和耐旱性作为支柱复杂性进化过程中的关键选择压力;但是,这些假说往往将支柱从整个植物的发育背景中分离出来,忽略了维管形态和嫩枝形态之间的潜在共变关系。此外,预期模式与观察到的数据之间的不一致也对适应性假说提出了挑战,从而无法全面解释石柱的进化。虽然本体发生以前已被认为是石柱多样化的一个因素,但它尚未被完全纳入一个全面的框架。在这里,我们综合了150年来对石龙子形态的研究,结合发育、生理和系统发育数据,提出了石龙子进化的本体发育假说。该假说认为,叶柄形态是整个植物本体进化的综合特征,而不是通过适应性模式的直接选择而形成的性状。这一视角的转变为理解石柱形态的决定因素提供了一个最新框架,并使今后的工作重点放在提出有关初级维管结构的进化和功能的更尖锐的问题上。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ontogenetic correlates, not direct adaptation, explain the evolution of stelar morphology
SummaryThe primary vascular system of plants (the stele) has attracted interest from paleobotanists, developmental biologists, systematists, and physiologists for nearly two centuries. Ferns, with their diverse stelar morphology, deep evolutionary history, and prominent fossil record, have been a major focus in studies of the stele. To explain the diversity of stelar morphology, past adaptive hypotheses have invoked biomechanics, hydraulics, and drought tolerance as key selection pressures in the evolution of stelar complexity; but, these hypotheses often isolate the stele from a whole‐plant developmental context, ignoring potential covariation between vascular patterning and shoot morphology. Furthermore, incongruence between expected patterns and observed data challenge adaptive hypotheses, precluding a comprehensive explanation of stelar evolution. While ontogeny has been previously recognized as a factor in stelar diversification, it has not been fully integrated into a comprehensive framework. Here we synthesize 150‐years of research on stelar morphology, incorporating developmental, physiological, and phylogenetic data to present the ontogenetic hypothesis of stelar evolution. This hypothesis posits that stelar morphology is an integrated feature of whole‐plant ontogeny, not a trait shaped by direct selection for adaptive patterns. This shift in perspective provides an updated framework for understanding the determinants of stelar morphology and focusses future efforts to ask more incisive questions about the evolution and function of primary vascular architecture.
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来源期刊
New Phytologist
New Phytologist 生物-植物科学
自引率
5.30%
发文量
728
期刊介绍: New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.
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