• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肉质植物。

Succulent plants.

机构信息

Physiological Ecology, Department of Plant Sciences, University of Cambridge, Cambridge, UK.

Physiological Ecology, Department of Plant Sciences, University of Cambridge, Cambridge, UK.

出版信息

Curr Biol. 2017 Sep 11;27(17):R890-R896. doi: 10.1016/j.cub.2017.03.021.

DOI:10.1016/j.cub.2017.03.021
PMID:28898660
Abstract

The peculiar morphologies of succulent plants have been variously considered as grotesque monstrosities and exotic curiosities, but succulents have always been perceived as unique. The succulent syndrome is considered to be one of the most remarkable examples of convergent evolution across the plant kingdom. Common to all succulents is the presence of large cells for water storage. However, cellular succulence can occur in any vegetative plant organ, with the level of succulence in roots, stems, and leaves being subject to a certain degree of evolutionary coordination. Furthermore, cellular succulence scales up to morphological succulence according to various anatomical schemes that confer contrasting functional characteristics. This means that succulence is associated with a broad range of ecophysiological strategies and occurs in plants that have evolved in many different environments.

摘要

肉质植物奇特的形态曾被认为是怪诞的畸形和奇异的奇观,但它们一直被视为独特的存在。肉质综合征被认为是植物界趋同进化最显著的例子之一。所有肉质植物的共同特点是存在用于储水的大细胞。然而,细胞肉质可以发生在任何营养植物器官中,根、茎和叶的肉质程度在一定程度上受到进化协调的影响。此外,根据赋予不同功能特性的各种解剖方案,细胞肉质会上升为形态肉质。这意味着肉质与广泛的生理生态策略有关,存在于许多不同环境中进化而来的植物中。

相似文献

1
Succulent plants.肉质植物。
Curr Biol. 2017 Sep 11;27(17):R890-R896. doi: 10.1016/j.cub.2017.03.021.
2
Secrets of succulence.多汁植物的秘密。
J Exp Bot. 2017 Apr 1;68(9):2121-2134. doi: 10.1093/jxb/erx096.
3
Plant venation: from succulence to succulents.植物脉序:从多汁植物到肉质植物。
Curr Biol. 2013 May 6;23(9):R340-1. doi: 10.1016/j.cub.2013.03.060.
4
Insights on the evolution of plant succulence from a remarkable radiation in Madagascar (Euphorbia).从马达加斯加(大戟属植物)的显著辐射中洞察植物肉质的进化
Syst Biol. 2014 Sep;63(5):697-711. doi: 10.1093/sysbio/syu035. Epub 2014 May 22.
5
Repeated origin of three-dimensional leaf venation releases constraints on the evolution of succulence in plants.三维叶脉的重复起源释放了植物肉质化进化的限制。
Curr Biol. 2013 Apr 22;23(8):722-6. doi: 10.1016/j.cub.2013.03.029. Epub 2013 Apr 11.
6
Tissue succulence in plants: Carrying water for climate change.植物组织多汁性:为气候变化输送水分。
J Plant Physiol. 2023 Oct;289:154081. doi: 10.1016/j.jplph.2023.154081. Epub 2023 Sep 4.
7
Are cell wall traits a component of the succulent syndrome?细胞壁特征是肉质化综合症的一个组成部分吗?
Front Plant Sci. 2022 Nov 25;13:1043429. doi: 10.3389/fpls.2022.1043429. eCollection 2022.
8
[Evolution of succulent Senecioneae (Asteraceae) of Southern Africa].[南非肉质千里光族(菊科)的演化]
Zh Obshch Biol. 2014 Jan-Feb;75(1):25-37.
9
Evolutionary origins, macroevolutionary dynamics, and climatic niche space of the succulent plant syndrome in the Caryophyllales.石竹目多肉植物综合征的进化起源、宏观进化动态及气候生态位空间
J Exp Bot. 2025 Jan 10;76(2):576-593. doi: 10.1093/jxb/erae428.
10
Evolution of unusual morphologies in Lentibulariaceae (bladderworts and allies) and Podostemaceae (river-weeds): a pictorial report at the interface of developmental biology and morphological diversification.狸藻科(狸藻及其近缘植物)和川苔草科(河苔草类)中异常形态的演化:发育生物学与形态多样性界面的图文报告
Ann Bot. 2016 Apr;117(5):811-32. doi: 10.1093/aob/mcv172. Epub 2015 Nov 20.

引用本文的文献

1
Floristic composition of Shamansir mountain, West Saudi Arabia, as sustainable economic resources.沙特阿拉伯西部沙曼西尔山的植物区系组成作为可持续经济资源。
Sci Rep. 2025 May 14;15(1):16800. doi: 10.1038/s41598-025-00441-4.
2
Dynamic in vivo monitoring of granum structural changes of Ctenanthe setosa (Roscoe) Eichler during drought stress and subsequent recovery.干旱胁迫及后续恢复过程中锦竹芋(Ctenanthe setosa (Roscoe) Eichler)叶绿体基粒结构变化的动态体内监测
Physiol Plant. 2025 Jan-Feb;177(1):e14621. doi: 10.1111/ppl.14621.
3
Halophytic succulence is a driver of the leaf non-structural carbohydrate contents in plants in the arid and hyper-arid deserts of northwestern China.
盐生肉质化是中国西北干旱和极端干旱沙漠地区植物叶片非结构性碳水化合物含量的一个驱动因素。
Ann Bot. 2025 Feb 19;135(3):565-576. doi: 10.1093/aob/mcae185.
4
Untangling poikilohydry and desiccation tolerance: evolutionary and macroecological drivers in ferns.解析变水现象与耐旱性:蕨类植物的进化和宏观生态驱动因素
Ann Bot. 2024 Dec 31;134(7):1139-1150. doi: 10.1093/aob/mcae167.
5
Identifying the multiple drivers of cactus diversification.鉴定仙人掌多样化的多种驱动因素。
Nat Commun. 2024 Aug 23;15(1):7282. doi: 10.1038/s41467-024-51666-2.
6
Divergent structural leaf trait spectra in succulent versus non-succulent plant taxa.肉质与非肉质植物类群的结构叶性状谱的分异。
Ann Bot. 2024 Aug 22;134(3):491-500. doi: 10.1093/aob/mcae093.
7
The phytomicrobiome: solving plant stress tolerance under climate change.植物微生物组:应对气候变化下的植物胁迫耐受性
Front Plant Sci. 2023 Sep 7;14:1219366. doi: 10.3389/fpls.2023.1219366. eCollection 2023.
8
Atmospheric CO2 decline and the timing of CAM plant evolution.大气 CO2 下降与 CAM 植物进化的时间。
Ann Bot. 2023 Nov 25;132(4):753-770. doi: 10.1093/aob/mcad122.
9
A new approach to an old problem: how to categorize the habit of ferns and lycophytes.一种新方法解决老问题:如何给蕨类植物和石松类植物的习性分类。
Ann Bot. 2023 Nov 23;132(3):513-522. doi: 10.1093/aob/mcad128.
10
The Agavoideae: an emergent model clade for CAM evolutionary biology.龙舌兰超族:CAM 进化生物学中的一个新兴模式类群。
Ann Bot. 2023 Nov 25;132(4):727-737. doi: 10.1093/aob/mcad062.