Ecological change and conflict reduction led to a social circulatory system in ants.

IF 5.1 1区 生物学 Q1 BIOLOGY Communications Biology Pub Date : 2025-02-16 DOI:10.1038/s42003-025-07688-7
Marie-Pierre Meurville, Daniele Silvestro, Adria C LeBoeuf
{"title":"Ecological change and conflict reduction led to a social circulatory system in ants.","authors":"Marie-Pierre Meurville, Daniele Silvestro, Adria C LeBoeuf","doi":"10.1038/s42003-025-07688-7","DOIUrl":null,"url":null,"abstract":"<p><p>Behavioral innovations can be ecologically transformative for lineages that perform them and for their associated communities. Many ecologically dominant, superorganismal, and speciose ant lineages use mouth-to-mouth social regurgitation behavior - stomodeal trophallaxis - to share exogenous and endogenous materials within colonies. This behavior is less common in other species-poor, less cooperative ant lineages. How and why trophallaxis evolved and fixed in only some ant clades remains unclear, and whether this trait could be indicative of superorganismality has yet to be established. Here we show that trophallaxis evolved in two main events, in non-doryline formicoids around 130 Ma and in some ponerines around 90 Ma, lineages that today encompass 86% of all ant species. We found that trophallaxis evolved in lineages that began drinking sugary liquids and that had reduced intra-colonial conflict by constraining worker reproductive potential. Evolution of trophallaxis increased net diversification. Causal models indicate that trophallaxis required low reproductive conflict and contributed to the large colony sizes of the ants that use it. This suggests that the evolution of social regurgitation was enabled by both social conflict reduction and opportunistic inclusion of nectar and honeydew in the ant diet during the shifts in terrestrial ecosystems toward flowering plants.</p>","PeriodicalId":10552,"journal":{"name":"Communications Biology","volume":"8 1","pages":"246"},"PeriodicalIF":5.1000,"publicationDate":"2025-02-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11830068/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Communications Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1038/s42003-025-07688-7","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Behavioral innovations can be ecologically transformative for lineages that perform them and for their associated communities. Many ecologically dominant, superorganismal, and speciose ant lineages use mouth-to-mouth social regurgitation behavior - stomodeal trophallaxis - to share exogenous and endogenous materials within colonies. This behavior is less common in other species-poor, less cooperative ant lineages. How and why trophallaxis evolved and fixed in only some ant clades remains unclear, and whether this trait could be indicative of superorganismality has yet to be established. Here we show that trophallaxis evolved in two main events, in non-doryline formicoids around 130 Ma and in some ponerines around 90 Ma, lineages that today encompass 86% of all ant species. We found that trophallaxis evolved in lineages that began drinking sugary liquids and that had reduced intra-colonial conflict by constraining worker reproductive potential. Evolution of trophallaxis increased net diversification. Causal models indicate that trophallaxis required low reproductive conflict and contributed to the large colony sizes of the ants that use it. This suggests that the evolution of social regurgitation was enabled by both social conflict reduction and opportunistic inclusion of nectar and honeydew in the ant diet during the shifts in terrestrial ecosystems toward flowering plants.

Abstract Image

Abstract Image

Abstract Image

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
生态变化和冲突减少导致了蚂蚁的社会循环系统。
行为创新对于执行行为创新的世系及其相关社区来说,具有生态变革作用。许多生态优势、超有机体和物种蚂蚁谱系使用口对口的社会反流行为-气孔滋养-在群体内共享外源性和内源性物质。这种行为在其他物种贫乏、不太合作的蚂蚁谱系中不太常见。目前尚不清楚营养是如何以及为什么只在一些蚂蚁分支中进化和固定下来的,而且这种特征是否表明了超有机体的存在也尚未确定。在这里,我们发现营养性在两个主要事件中进化,在130 Ma左右的非多线蚁类和90 Ma左右的一些多线蚁类中,今天包括86%的蚂蚁物种。我们发现,营养性在开始饮用含糖液体的谱系中进化,并通过限制工蚁的生殖潜力来减少殖民地内的冲突。营养层的进化增加了净多样化。因果模型表明,营养性需要低的繁殖冲突,并有助于使用它的蚂蚁的大群体规模。这表明,在陆地生态系统向开花植物转变的过程中,社会冲突的减少和蚂蚁饮食中花蜜和蜜露的机会性包含使得社会反流的进化成为可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Communications Biology
Communications Biology Medicine-Medicine (miscellaneous)
CiteScore
8.60
自引率
1.70%
发文量
1233
审稿时长
13 weeks
期刊介绍: Communications Biology is an open access journal from Nature Research publishing high-quality research, reviews and commentary in all areas of the biological sciences. Research papers published by the journal represent significant advances bringing new biological insight to a specialized area of research.
期刊最新文献
A spatiotemporal transcriptomic atlas of porcine (Sus scrofa) female early gonadal development. The coexistence of r and K strategy in a unicellular microalga Haematococcus lacustris. Widespread atypical response regulator SecR governs bacterial growth on methylamines through the serine cycle. A multidimensional framework for dissociating the neuroplasticity of auditory and early language deprivation. Single-cell transcriptome-wide Mendelian randomization during CD4+ T cell activation reveals immune-mediated mechanisms and drug targets for neuropsychiatric disorders.
×
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:604180095
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