• 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

波动的气候和饮食创新推动了长鼻目牙齿特征的棘轮进化。

Fluctuating climate and dietary innovation drove ratcheted evolution of proboscidean dental traits.

机构信息

Department of Geosciences and Geography, University of Helsinki, Helsinki, Finland.

Natural History Museum, London, UK.

出版信息

Nat Ecol Evol. 2023 Sep;7(9):1490-1502. doi: 10.1038/s41559-023-02151-4. Epub 2023 Aug 14.

DOI:10.1038/s41559-023-02151-4
PMID:37580434
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10482678/
Abstract

Identification of the selective forces that shaped adaptive phenotypes generally relies on current habitat and function, but these may differ from the context in which adaptations arose. Moreover, the fixation of adaptive change in a fluctuating environment and the mechanisms of long-term trends are still poorly understood, as is the role of behaviour in triggering these processes. Time series of fossils can provide evidence on these questions, but examples of individual lineages with adequate fossil and proxy data over extended periods are rare. Here, we present new data on proboscidean dental evolution in East Africa over the past 26 million years, tracking temporal patterns of morphological change in relation to proxy evidence of diet, vegetation and climate (aridity). We show that behavioural experimentation in diet is correlated with environmental context, and that major adaptive change in dental traits followed the changes in diet and environment but only after acquisition of functional innovations in the masticatory system. We partition traits by selective agent, showing that the acquisition of high, multiridged molars was primarily a response to an increase in open, arid environments with high dust accumulation, whereas enamel folding was more associated with the amount of grass in the diet. We further show that long-term trends in these features proceeded in a ratchet-like mode, alternating between directional change at times of high selective pressure and stasis when the selective regime reversed. This provides an explanation for morphology adapted to more extreme conditions than current usage (Liem's Paradox). Our study illustrates how, in fossil series with adequate stratigraphic control and proxy data, environmental and behavioural factors can be mapped on to time series of morphological change, illuminating the mode of acquisition of an adaptive complex.

摘要

鉴定塑造适应性表型的选择压力通常依赖于当前的栖息地和功能,但这些可能与适应性产生的背景不同。此外,在波动环境中固定适应性变化以及长期趋势的机制仍知之甚少,行为在引发这些过程中的作用也是如此。化石时间序列可以提供这些问题的证据,但具有足够化石和代理数据的个体谱系在较长时期内的例子很少。在这里,我们提出了过去 2600 万年东非长鼻目牙齿进化的新数据,追踪了形态变化与饮食、植被和气候(干旱)代理证据的时间模式。我们表明,饮食方面的行为实验与环境背景有关,而牙齿特征的主要适应性变化紧随饮食和环境的变化,但仅在咀嚼系统获得功能创新之后。我们通过选择性代理对特征进行分区,表明高、多脊状臼齿的获得主要是对高尘土堆积的开阔、干旱环境增加的反应,而牙釉质折叠与饮食中的草量更相关。我们进一步表明,这些特征的长期趋势以棘轮式模式进行,在高选择压力时期发生定向变化,而在选择机制反转时则处于停滞状态。这为适应比当前使用条件更极端条件的形态提供了一种解释(利姆悖论)。我们的研究说明了在具有足够地层控制和代理数据的化石系列中,环境和行为因素如何映射到形态变化的时间序列上,阐明了获得适应性复合体的方式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/40ea3af40f1f/41559_2023_2151_Fig14_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/78e078d6b475/41559_2023_2151_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/65feea988443/41559_2023_2151_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/6be591cadbb5/41559_2023_2151_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/3a5b0c5119a4/41559_2023_2151_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/3b2ac432c3b3/41559_2023_2151_Fig5_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/8188d8741028/41559_2023_2151_Fig6_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/44669b75295b/41559_2023_2151_Fig7_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/369a1bc094a6/41559_2023_2151_Fig8_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/d7f42375c190/41559_2023_2151_Fig9_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/1f16146dfe85/41559_2023_2151_Fig10_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/cc610f9051a2/41559_2023_2151_Fig11_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/13fd95f87695/41559_2023_2151_Fig12_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/79c60bb48cc6/41559_2023_2151_Fig13_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/40ea3af40f1f/41559_2023_2151_Fig14_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/78e078d6b475/41559_2023_2151_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/65feea988443/41559_2023_2151_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/6be591cadbb5/41559_2023_2151_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/3a5b0c5119a4/41559_2023_2151_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/3b2ac432c3b3/41559_2023_2151_Fig5_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/8188d8741028/41559_2023_2151_Fig6_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/44669b75295b/41559_2023_2151_Fig7_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/369a1bc094a6/41559_2023_2151_Fig8_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/d7f42375c190/41559_2023_2151_Fig9_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/1f16146dfe85/41559_2023_2151_Fig10_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/cc610f9051a2/41559_2023_2151_Fig11_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/13fd95f87695/41559_2023_2151_Fig12_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/79c60bb48cc6/41559_2023_2151_Fig13_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e1f/10482678/40ea3af40f1f/41559_2023_2151_Fig14_ESM.jpg

相似文献

1
Fluctuating climate and dietary innovation drove ratcheted evolution of proboscidean dental traits.波动的气候和饮食创新推动了长鼻目牙齿特征的棘轮进化。
Nat Ecol Evol. 2023 Sep;7(9):1490-1502. doi: 10.1038/s41559-023-02151-4. Epub 2023 Aug 14.
2
The role of behaviour in adaptive morphological evolution of African proboscideans.行为在非洲长鼻目动物适应性形态进化中的作用。
Nature. 2013 Aug 15;500(7462):331-4. doi: 10.1038/nature12275. Epub 2013 Jun 26.
3
Author Correction: Fluctuating climate and dietary innovation drove ratcheted evolution of proboscidean dental traits.作者更正:气候变化与饮食创新推动长鼻目动物牙齿特征的棘轮式进化。
Nat Ecol Evol. 2023 Oct;7(10):1740. doi: 10.1038/s41559-023-02204-8.
4
Morphological evolution, ecological diversification and climate change in rodents.啮齿动物的形态演变、生态多样化与气候变化
Proc Biol Sci. 2005 Mar 22;272(1563):609-17. doi: 10.1098/rspb.2004.2992.
5
Alternating high and low climate variability: The context of natural selection and speciation in Plio-Pleistocene hominin evolution.高低交替的气候变异性:上新世-更新世古人类进化中自然选择和物种形成的背景。
J Hum Evol. 2015 Oct;87:5-20. doi: 10.1016/j.jhevol.2015.06.014. Epub 2015 Aug 25.
6
Tempo does not correlate with mode in the fossil record.在化石记录中,节奏与模式并不相关。
Evolution. 2016 Dec;70(12):2678-2689. doi: 10.1111/evo.13090. Epub 2016 Nov 9.
7
Ecological change in the lower Omo Valley around 2.8 Ma.约 280 万年前下奥莫河谷的生态变化。
Biol Lett. 2012 Dec 12;9(1):20120890. doi: 10.1098/rsbl.2012.0890. Print 2013 Feb 23.
8
Connecting local environmental sequences to global climate patterns: evidence from the hominin-bearing Hadar Formation, Ethiopia.将当地环境序列与全球气候模式相联系:来自埃塞俄比亚含古人类化石的哈达尔组的证据。
J Hum Evol. 2007 Nov;53(5):515-27. doi: 10.1016/j.jhevol.2007.05.015. Epub 2007 Oct 17.
9
Aridity and hominin environments.干旱与古人类环境。
Proc Natl Acad Sci U S A. 2017 Jul 11;114(28):7331-7336. doi: 10.1073/pnas.1700597114. Epub 2017 Jun 26.
10
The relative importance of directional change, random walks, and stasis in the evolution of fossil lineages.在化石谱系演化中,方向变化、随机游走和停滞的相对重要性。
Proc Natl Acad Sci U S A. 2007 Nov 20;104(47):18404-8. doi: 10.1073/pnas.0704088104. Epub 2007 Nov 14.

引用本文的文献

1
Six million years of vole dental evolution shaped by tooth development.六百万年的田鼠牙齿进化受牙齿发育影响。
Proc Natl Acad Sci U S A. 2025 Aug 5;122(31):e2505624122. doi: 10.1073/pnas.2505624122. Epub 2025 Jul 31.
2
Trait-mediated speciation and human-driven extinctions in proboscideans revealed by unsupervised Bayesian neural networks.无监督贝叶斯神经网络揭示了长鼻目动物的性状介导物种形成和人类驱动的灭绝。
Sci Adv. 2024 Jul 26;10(30):eadl2643. doi: 10.1126/sciadv.adl2643. Epub 2024 Jul 24.

本文引用的文献

1
Oldest evidence of abundant C grasses and habitat heterogeneity in eastern Africa.东非丰富的 C 草和生境异质性的最古老证据。
Science. 2023 Apr 14;380(6641):173-177. doi: 10.1126/science.abq2834. Epub 2023 Apr 13.
2
Palaeodietary traits of large mammals from the middle Miocene of Gračanica (Bugojno Basin, Bosnia-Herzegovina).来自格拉查尼察(波斯尼亚和黑塞哥维那布戈伊诺盆地)中新世中期大型哺乳动物的古饮食特征。
Paleobiodivers Paleoenviron. 2020;100(2):457-477. doi: 10.1007/s12549-020-00435-2. Epub 2020 Jun 11.
3
Early hominins evolved within non-analog ecosystems.
早期人类在非同源生态系统中进化。
Proc Natl Acad Sci U S A. 2019 Oct 22;116(43):21478-21483. doi: 10.1073/pnas.1909284116. Epub 2019 Oct 7.
4
Ecological and hydroclimate responses to strengthening of the Hadley circulation in South America during the Late Miocene cooling.晚中新世冷却期间南美洲 Hadley 环流加强的生态和水文气候响应。
Proc Natl Acad Sci U S A. 2019 May 14;116(20):9747-9752. doi: 10.1073/pnas.1810721116. Epub 2019 Apr 29.
5
Scientists rise up against statistical significance.科学家们奋起反对统计显著性。
Nature. 2019 Mar;567(7748):305-307. doi: 10.1038/d41586-019-00857-9.
6
Plio-Pleistocene decline of African megaherbivores: No evidence for ancient hominin impacts.更新世早期至中期非洲大型食草动物的减少:没有证据表明远古人类活动的影响。
Science. 2018 Nov 23;362(6417):938-941. doi: 10.1126/science.aau2728.
7
A grazing Gomphotherium in Middle Miocene Central Asia, 10 million years prior to the origin of the Elephantidae.中亚中新世的一种食草恐象,比象类起源早 1000 万年。
Sci Rep. 2018 May 16;8(1):7640. doi: 10.1038/s41598-018-25909-4.
8
EVOLUTION OF MASTICATION IN THE ELEPHANTIDAE.象科动物咀嚼功能的演化
Evolution. 1972 Dec;26(4):638-658. doi: 10.1111/j.1558-5646.1972.tb01970.x.
9
Browsing and grazing in elephants: the isotope record of modern and fossil proboscideans.大象的觅食与啃食:现代及化石长鼻目动物的同位素记录
Oecologia. 1999 Aug;120(3):364-374. doi: 10.1007/s004420050869.
10
Untangling the environmental from the dietary: dust does not matter.区分环境因素和饮食因素:灰尘并无影响。
Proc Biol Sci. 2016 Sep 14;283(1838). doi: 10.1098/rspb.2016.1032.