• 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

为什么小雄性能有大精子:二态鱿鱼精子与替代交配行为有关。

Why small males have big sperm: dimorphic squid sperm linked to alternative mating behaviours.

机构信息

Institute of Biological, Environmental and Rural Sciences, Aberystwyth University, Penglais, Aberystwyth, SY23 3DA, UK.

出版信息

BMC Evol Biol. 2011 Aug 10;11:236. doi: 10.1186/1471-2148-11-236.

DOI:10.1186/1471-2148-11-236
PMID:21831296
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3176235/
Abstract

BACKGROUND

Sperm cells are the target of strong sexual selection that may drive changes in sperm structure and function to maximize fertilisation success. Sperm evolution is regarded to be one of the major consequences of sperm competition in polyandrous species, however it can also be driven by adaptation to the environmental conditions at the site of fertilization. Strong stabilizing selection limits intra-specific variation, and therefore polymorphism, among fertile sperm (eusperm). Here we analyzed reproductive morphology differences among males employing characteristic alternative mating behaviours, and so potentially different conditions of sperm competition and fertilization environment, in the squid Loligo bleekeri.

RESULTS

Large consort males transfer smaller (average total length = 73 μm) sperm to a female's internal sperm storage location, inside the oviduct; whereas small sneaker males transfer larger (99 μm) sperm to an external location around the seminal receptacle near the mouth. No significant difference in swimming speed was observed between consort and sneaker sperm. Furthermore, sperm precedence in the seminal receptacle was not biased toward longer sperm, suggesting no evidence for large sperm being favoured in competition for space in the sperm storage organ among sneaker males.

CONCLUSIONS

Here we report the first case, in the squid Loligo bleekeri, where distinctly dimorphic eusperm are produced by different sized males that employ alternative mating behaviours. Our results found no evidence that the distinct sperm dimorphism was driven by between- and within-tactic sperm competition. We propose that presence of alternative fertilization environments with distinct characteristics (i.e. internal or external), whether or not in combination with the effects of sperm competition, can drive the disruptive evolution of sperm size.

摘要

背景

精子是强烈的性选择的目标,这可能导致精子结构和功能的变化,以最大限度地提高受精成功的机会。精子进化被认为是多配偶物种中精子竞争的主要后果之一,但它也可以通过适应受精地点的环境条件来驱动。强烈的稳定选择限制了可育精子(正常精子)的种内变异,因此多态性有限。在这里,我们分析了利用特征性替代交配行为的雄性之间的生殖形态差异,因此可能存在不同的精子竞争和受精环境条件,在鱿鱼 Loligo bleekeri 中。

结果

大配偶雄性将较小的(平均总长度= 73μm)精子转移到雌性的内部精子储存位置,在输卵管内;而小的 sneaker 雄性将较大的(99μm)精子转移到外部位置,在靠近嘴的精液接收器周围。在游泳速度方面,consort 和 sneaker 精子之间没有观察到显著差异。此外,在精液接收器中,精子优先顺序不受长精子的影响,这表明在 sneaker 雄性中,没有证据表明大精子在争夺精子储存器官中的空间竞争中具有优势。

结论

在这里,我们报告了第一个案例,在鱿鱼 Loligo bleekeri 中,不同大小的雄性产生明显不同的正常精子,这些雄性采用替代交配行为。我们的研究结果没有发现明显的精子二态性是由种内和种间精子竞争驱动的证据。我们提出,替代受精环境的存在,具有不同的特征(即内部或外部),无论是否与精子竞争的影响相结合,都可以驱动精子大小的破坏进化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9b0/3176235/c341a8070393/1471-2148-11-236-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9b0/3176235/dec83b96f663/1471-2148-11-236-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9b0/3176235/f5c65b964b0e/1471-2148-11-236-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9b0/3176235/0e3875b43bc2/1471-2148-11-236-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9b0/3176235/c341a8070393/1471-2148-11-236-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9b0/3176235/dec83b96f663/1471-2148-11-236-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9b0/3176235/f5c65b964b0e/1471-2148-11-236-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9b0/3176235/0e3875b43bc2/1471-2148-11-236-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9b0/3176235/c341a8070393/1471-2148-11-236-4.jpg

相似文献

1
Why small males have big sperm: dimorphic squid sperm linked to alternative mating behaviours.为什么小雄性能有大精子:二态鱿鱼精子与替代交配行为有关。
BMC Evol Biol. 2011 Aug 10;11:236. doi: 10.1186/1471-2148-11-236.
2
The different types of sperm morphology and behavior within a single species: Why do sperm of squid sneaker males form a cluster?单一物种内精子的不同形态和行为类型:为什么鱿鱼偷腥雄体的精子会形成簇状?
Commun Integr Biol. 2013 Nov 1;6(6):e26729. doi: 10.4161/cib.26729. Epub 2013 Oct 9.
3
Sperm competition risk affects ejaculate strategy in terms of sperm number but not sperm size in squid.精子竞争风险会影响鱿鱼的精子数量策略,但不会影响精子大小策略。
J Evol Biol. 2021 Sep;34(9):1352-1361. doi: 10.1111/jeb.13894. Epub 2021 Jul 4.
4
Integrative omics analysis reveals differentially distributed proteins in dimorphic euspermatozoa of the squid, Loligo bleekeri.整合组学分析揭示了鱿鱼 Loligo bleekeri 二态精原细胞中差异分布的蛋白质。
Biochem Biophys Res Commun. 2014 Aug 1;450(3):1218-24. doi: 10.1016/j.bbrc.2014.04.076. Epub 2014 Apr 24.
5
Context-dependent behavioural plasticity compromises disruptive selection of sperm traits in squid.情境依赖的行为可塑性损害了鱿鱼精子特征的破坏性选择。
PLoS One. 2021 Aug 30;16(8):e0256745. doi: 10.1371/journal.pone.0256745. eCollection 2021.
6
Dimorphic ejaculates and sperm release strategies associated with alternative mating behaviors in the squid.双态射精与鱿鱼替代交配行为相关的精子释放策略。
J Morphol. 2017 Nov;278(11):1490-1505. doi: 10.1002/jmor.20726. Epub 2017 Jul 18.
7
Shorter sperm confer higher competitive fertilization success.较短的精子具有更高的竞争性受精成功率。
Evolution. 2007 Apr;61(4):816-24. doi: 10.1111/j.1558-5646.2007.00084.x.
8
A mating plug in a squid? Sneaker spermatophores can block the female sperm-storage organ in Doryteuthis plei.鱿鱼体内有交配栓?在杜氏枪乌贼中,偷精者的精荚能堵塞雌性的精子储存器官。
Zoology (Jena). 2018 Oct;130:47-56. doi: 10.1016/j.zool.2018.08.002. Epub 2018 Sep 8.
9
Sperm from sneaker male squids exhibit chemotactic swarming to CO₂.运动鞋男乌贼的精子对二氧化碳表现出趋化性的群体游动。
Curr Biol. 2013 May 6;23(9):775-81. doi: 10.1016/j.cub.2013.03.040. Epub 2013 Apr 11.
10
Sneaker Male Squid Produce Long-lived Spermatozoa by Modulating Their Energy Metabolism.运动鞋雄性鱿鱼通过调节能量代谢产生寿命长的精子。
J Biol Chem. 2016 Sep 9;291(37):19324-34. doi: 10.1074/jbc.M116.737494. Epub 2016 Jul 6.

引用本文的文献

1
Within-female sperm allocation in is associated with polyandry and male-biased sex ratio.雌性体内的精子分配与一妻多夫制和雄性偏向的性别比例有关。
MicroPubl Biol. 2025 Jul 2;2025. doi: 10.17912/micropub.biology.001538. eCollection 2025.
2
Alternative mating pattern in is associated with polyandry and male-biased sex ratio.[物种名称]中的替代交配模式与一妻多夫制和雄性偏向的性别比例有关。
MicroPubl Biol. 2025 Jan 8;2025. doi: 10.17912/micropub.biology.001424. eCollection 2025.
3
Males conditionally inseminate at three female body locations according to female mating history and female maturity status in a squid.

本文引用的文献

1
Behavioral Dynamics That Would Lead to Multiple Paternity within Egg Capsules of the Squid Loligo pealei.导致枪乌贼(Loligo pealei)卵囊中出现多重父系的行为动态。
Biol Bull. 1997 Oct;193(2):212-214. doi: 10.1086/BBLv193n2p212.
2
Pronounced within-individual plasticity in sperm morphometry across social environments.个体内精子形态测量在社会环境中的明显可塑性。
Evolution. 2010 Jun;64(6):1634-43. doi: 10.1111/j.1558-5646.2009.00924.x. Epub 2009 Dec 10.
3
Generalized linear mixed models: a practical guide for ecology and evolution.
在鱿鱼中,雄性根据雌性的交配史和成熟状态,有条件地在三个雌性身体部位进行授精。
Sci Rep. 2024 May 22;14(1):11702. doi: 10.1038/s41598-024-62062-7.
4
Squid male alternative reproductive tactics are determined by birth date.鱿鱼雄性的替代生殖策略由出生日期决定。
Proc Biol Sci. 2024 Apr 30;291(2021):20240156. doi: 10.1098/rspb.2024.0156. Epub 2024 Apr 24.
5
Male alternative reproductive tactics and sperm competition: a meta-analysis.雄性替代生殖策略与精子竞争:一项荟萃分析。
Biol Rev Camb Philos Soc. 2022 Aug;97(4):1365-1388. doi: 10.1111/brv.12846. Epub 2022 Feb 28.
6
Context-dependent behavioural plasticity compromises disruptive selection of sperm traits in squid.情境依赖的行为可塑性损害了鱿鱼精子特征的破坏性选择。
PLoS One. 2021 Aug 30;16(8):e0256745. doi: 10.1371/journal.pone.0256745. eCollection 2021.
7
Sperm and alternative reproductive tactics: a review of existing theory and empirical data.精子和替代性生殖策略:现有理论和实证数据的综述。
Philos Trans R Soc Lond B Biol Sci. 2020 Dec 7;375(1813):20200075. doi: 10.1098/rstb.2020.0075. Epub 2020 Oct 19.
8
Rare polyandry and common monogamy in the firefly squid, Watasenia scintillans.罕见的一妻多夫制和常见的一夫一妻制存在于萤乌贼(Watasenia scintillans)中。
Sci Rep. 2020 Jul 3;10(1):10962. doi: 10.1038/s41598-020-68006-1.
9
Differences and Similarities: The Richness of Comparative Sperm Physiology.差异与相似:比较精子生理学的丰富内涵。
Physiology (Bethesda). 2020 May 1;35(3):196-208. doi: 10.1152/physiol.00033.2019.
10
Male Alternative Reproductive Tactics and Associated Evolution of Anatomical Characteristics in Loliginid Squid.枪乌贼科鱿鱼的雄性替代生殖策略及相关解剖特征的进化
Front Physiol. 2019 Oct 15;10:1281. doi: 10.3389/fphys.2019.01281. eCollection 2019.
广义线性混合模型:生态学与进化实用指南
Trends Ecol Evol. 2009 Mar;24(3):127-35. doi: 10.1016/j.tree.2008.10.008.
4
Female promiscuity promotes the evolution of faster sperm in cichlid fishes.雌性滥交促进了丽鱼科鱼类精子更快的进化。
Proc Natl Acad Sci U S A. 2009 Jan 27;106(4):1128-32. doi: 10.1073/pnas.0809990106. Epub 2009 Jan 21.
5
Sperm competition in fishes: the evolution of testis size and ejaculate characteristics.鱼类中的精子竞争:睾丸大小与射精特征的进化
Am Nat. 1997 May;149(5):933-54. doi: 10.1086/286031.
6
Implications of diversity in sperm size and function for sperm competition and fertility.精子大小和功能的多样性对精子竞争和生育能力的影响。
Int J Dev Biol. 2008;52(5-6):439-47. doi: 10.1387/ijdb.082595mg.
7
Postcopulatory sexual selection is associated with reduced variation in sperm morphology.交配有性选择与精子形态变异减少有关。
PLoS One. 2007 May 2;2(5):e413. doi: 10.1371/journal.pone.0000413.
8
Sperm in competition: not playing by the numbers.精子在竞争中:并非按数量行事。
Trends Ecol Evol. 2005 Jan;20(1):46-53. doi: 10.1016/j.tree.2004.10.011. Epub 2004 Nov 6.
9
Post-mating clutch piracy in an amphibian.一种两栖动物的交配后偷卵行为。
Nature. 2004 Sep 16;431(7006):305-8. doi: 10.1038/nature02879.
10
Spermatozoal traits and sperm competition in Atlantic salmon: relative sperm velocity is the primary determinant of fertilization success.大西洋鲑鱼的精子特征与精子竞争:相对精子速度是受精成功的主要决定因素。
Curr Biol. 2004 Jan 6;14(1):44-7.