获得光营养作为混合营养的进化途径。

IF 2.4 2区 环境科学与生态学 Q2 ECOLOGY American Naturalist Pub Date : 2023-10-01 Epub Date: 2023-08-29 DOI:10.1086/725918
Alexandra L Brown, Grace A Casarez, Holly V Moeller
{"title":"获得光营养作为混合营养的进化途径。","authors":"Alexandra L Brown, Grace A Casarez, Holly V Moeller","doi":"10.1086/725918","DOIUrl":null,"url":null,"abstract":"<p><p>AbstractAcquired photosynthesis transforms genotypically heterotrophic lineages into autotrophs. Transient acquisitions of eukaryotic chloroplasts may provide key evolutionary insight into the endosymbiosis process-the hypothesized mechanism by which eukaryotic cells obtained new functions via organelle retention. Here, we use an eco-evolutionary model to study the environmental conditions under which chloroplast retention is evolutionarily favorable. We focus on kleptoplastidic lineages-which steal functional chloroplasts from their prey-as hypothetical evolutionary intermediates. Our adaptive dynamics analysis reveals a spectrum of evolutionarily stable strategies ranging from phagotrophy to phototrophy to obligate kleptoplasty. Our model suggests that a low-light niche and weak (or absent) trade-offs between chloroplast retention and overall digestive ability favor the evolution of phototrophy. In contrast, when consumers experience strong trade-offs, obligate kleptoplasty emerges as an evolutionary end point. Therefore, the preevolved trade-offs that underlie an evolving lineage's physiology will likely constrain its evolutionary trajectory.</p>","PeriodicalId":50800,"journal":{"name":"American Naturalist","volume":"202 4","pages":"458-470"},"PeriodicalIF":2.4000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Acquired Phototrophy as an Evolutionary Path to Mixotrophy.\",\"authors\":\"Alexandra L Brown, Grace A Casarez, Holly V Moeller\",\"doi\":\"10.1086/725918\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>AbstractAcquired photosynthesis transforms genotypically heterotrophic lineages into autotrophs. Transient acquisitions of eukaryotic chloroplasts may provide key evolutionary insight into the endosymbiosis process-the hypothesized mechanism by which eukaryotic cells obtained new functions via organelle retention. Here, we use an eco-evolutionary model to study the environmental conditions under which chloroplast retention is evolutionarily favorable. We focus on kleptoplastidic lineages-which steal functional chloroplasts from their prey-as hypothetical evolutionary intermediates. Our adaptive dynamics analysis reveals a spectrum of evolutionarily stable strategies ranging from phagotrophy to phototrophy to obligate kleptoplasty. Our model suggests that a low-light niche and weak (or absent) trade-offs between chloroplast retention and overall digestive ability favor the evolution of phototrophy. In contrast, when consumers experience strong trade-offs, obligate kleptoplasty emerges as an evolutionary end point. Therefore, the preevolved trade-offs that underlie an evolving lineage's physiology will likely constrain its evolutionary trajectory.</p>\",\"PeriodicalId\":50800,\"journal\":{\"name\":\"American Naturalist\",\"volume\":\"202 4\",\"pages\":\"458-470\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2023-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American Naturalist\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://doi.org/10.1086/725918\",\"RegionNum\":2,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2023/8/29 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"ECOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Naturalist","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1086/725918","RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/8/29 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

获得性光合作用将基因型异养谱系转化为自养生物。真核细胞叶绿体的短暂获得可能为内共生过程提供关键的进化见解,内共生过程是真核细胞通过细胞器保留获得新功能的假设机制。在这里,我们使用生态进化模型来研究叶绿体保留在进化上有利的环境条件。我们关注的是盗塑性谱系,它们从猎物身上窃取功能叶绿体,作为假设的进化中间产物。我们的适应性动力学分析揭示了一系列进化稳定的策略,从自噬性到光养性再到专性盗贼成形术。我们的模型表明,低光生态位和叶绿体保留和整体消化能力之间的弱(或不存在)权衡有利于光营养的进化。相比之下,当消费者经历了强烈的权衡时,义务性眼睑整形术就成为了进化的终点。因此,作为进化谱系生理学基础的预先进化的权衡可能会限制其进化轨迹。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Acquired Phototrophy as an Evolutionary Path to Mixotrophy.

AbstractAcquired photosynthesis transforms genotypically heterotrophic lineages into autotrophs. Transient acquisitions of eukaryotic chloroplasts may provide key evolutionary insight into the endosymbiosis process-the hypothesized mechanism by which eukaryotic cells obtained new functions via organelle retention. Here, we use an eco-evolutionary model to study the environmental conditions under which chloroplast retention is evolutionarily favorable. We focus on kleptoplastidic lineages-which steal functional chloroplasts from their prey-as hypothetical evolutionary intermediates. Our adaptive dynamics analysis reveals a spectrum of evolutionarily stable strategies ranging from phagotrophy to phototrophy to obligate kleptoplasty. Our model suggests that a low-light niche and weak (or absent) trade-offs between chloroplast retention and overall digestive ability favor the evolution of phototrophy. In contrast, when consumers experience strong trade-offs, obligate kleptoplasty emerges as an evolutionary end point. Therefore, the preevolved trade-offs that underlie an evolving lineage's physiology will likely constrain its evolutionary trajectory.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
American Naturalist
American Naturalist 环境科学-进化生物学
CiteScore
5.40
自引率
3.40%
发文量
194
审稿时长
3 months
期刊介绍: Since its inception in 1867, The American Naturalist has maintained its position as one of the world''s premier peer-reviewed publications in ecology, evolution, and behavior research. Its goals are to publish articles that are of broad interest to the readership, pose new and significant problems, introduce novel subjects, develop conceptual unification, and change the way people think. AmNat emphasizes sophisticated methodologies and innovative theoretical syntheses—all in an effort to advance the knowledge of organic evolution and other broad biological principles.
期刊最新文献
Secretary's Report, 2024 : American Society of Naturalists. Treasurer's Report, 2023 : Statement of Activities For the Year Ending December 31, 2023. Bee Phenological Distributions Predicted by Inferring Vital Rates. Differential Survival and Background Selection in Cryptic Trunk-Dwelling Arthropods in Fire-Prone Environments. Natural Selection after Severe Winter Favors Larger and Duller Bluebirds.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1