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Plant hydraulic architecture through time: lessons and questions on the evolution of vascular systems

机译:植物液压建筑通过时间:关于血管系统演化的课程和问题

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Studies of anatomically preserved fossils provide a wealth of information on the evolution of plant vascular systems through time, from the oldest evidence of vascular plants more than 400 million years ago to the rise of the modern angiosperm-dominated flora. In reviewing the key contributions of the fossil record, we discuss knowledge gaps and major outstanding questions about the processes attending the evolution of vascular systems. The appearance and diversification of early vascular plants in the late Silurian-Devonian was accompanied by the evolution of different types of tracheids, which initially improved the hydraulics of conduction but had less of an effect on mechanical support. This was followed in the Devonian and Carboniferous by an increase in complexity of the organization of primary vascular tissues, with different types of steles evolving in response to mechanical, hydraulic, and developmental regulatory constraints. Concurrently, secondary vascular tissues, such as wood, produced by unifacial or bifacial cambia are documented in a wide array of plant groups, including some that do not undergo secondary growth today. While wood production has traditionally been thought to have evolved independently in different lineages, accumulating evidence suggests that this taxonomic breadth reflects mosaic deployment of basic developmental mechanisms, some of which are derived by common ancestry. For most of vascular plant history, wood contained a single type of conducting element: tracheids (homoxyly). However, quantitative (e.g. diameter and length) and qualitative (e.g. pitting type) diversity of these tracheids allowed various taxa to cover a broad range of hydraulic properties. A second type of conducting elements, vessels, is first documented in an extinct late Permian (c. 260 Ma) group. While the putative hydraulic advantages of vessels are still debated, wood characterized by presence of vessels (heteroxyly) would become the dominant type, following the diversification of angiosperms during the Cretaceous.
机译:对解剖学保存的化石的研究提供了大量关于植物血管系统演变的信息,从而从血管植物的最古老的目的超过4亿年前到现代的血管植物主导的植物的崛起。在审查化石记录的关键贡献时,我们讨论了关于参加血管系统演变的过程的知识差距和主要的突出问题。早期宇建德农厂的早期血管植物的出现和多样化伴随着不同类型的行李箱的演变,最初改善了导通的液压,但对机械支撑效果较少。在德文人和石炭系中随着原发性血管组织组织的复杂性的增加,这是在牧群和石炭系中的复杂性,不同类型的硬盘响应机械,液压和发育监管限制而发展。同时,通过统一或双柬族的木材制造的二次血管组织被记录在各种植物基团中,包括今天不经历二次增长的群体。虽然木材生产传统上被认为是在不同的谱系中独立进化的,但积累的证据表明,这种分类管理广度反映了基本发展机制的马赛克部署,其中一些是普通祖先所衍生的。对于大多数血管植物历史,木材含有一种单一类型的导电元件:Trachids(母性)。然而,这些行李箱的定量(例如直径和长度)和定性(例如点烧蚀型)多样性允许各种征征涵盖各种液压性能。第二种类型的导电元件,血管,首先在灭绝的后期二叠纪(C.260 mA)组中记录。虽然血管的推定液压优点仍然讨论,但在白垩纪中的有道培素多样化之后,通过血管(杂族)的存在而表征的木材将成为主导型。

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