Correlated evolution of elaborate intromission mechanics during copulation between the sexes in leaf beetles.

IF 3.5 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Journal of The Royal Society Interface Pub Date : 2025-06-01 Epub Date: 2025-06-11 DOI:10.1098/rsif.2025.0155
Yoko Matsumura, Shayan Ramezanpour, Thomas van de Kamp, Stanislav Gorb, Alexander Kovalev, Hamed Rajabi
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引用次数: 0

Abstract

Diverse female and male genitalia have evolved. Although the evolutionary mechanisms behind this phenomenon have been studied extensively, the mechanical interactions between female and male genitalia are much less understood. Here, we provide an in-depth biomechanical study on the intromission of elongated tube-like female and male genitalia, termed the spermathecal duct and flagellum, in tortoise leaf beetles. Our findings reveal that this seemingly straightforward penetration mechanism is underpinned by structural and material specializations of the genitalia. We employed synchrotron-based micro-computed tomography and confocal laser scanning microscopy (CLSM) to visualize the precise mechanical interactions between female and male genitalia. Mechanical tests revealed a stiffness gradient within the flagellum and correlated stiffness variations between the sexes. Combining CLSM and cryo-microtome techniques, we characterized a heterogeneous material distribution at the flagellum tip; this specialization was more remarkable in the species with a more sclerotized spermathecal duct. Finite element analyses incorporating the observed material properties demonstrated that the observed material distribution reduced the penetration force required tremendously and dispersed the stress at the flagellum tip. This study unveils that structural and material adaptations in female and male genitalia have probably coevolved and highlights the importance of biomechanics in genital studies.

叶甲虫两性交配过程中精细渗透机制的相关进化。
不同的女性和男性生殖器已经进化。尽管这一现象背后的进化机制已经被广泛研究,但女性和男性生殖器之间的机械相互作用却鲜为人知。在这里,我们提供了一个深入的生物力学研究,在龟叶甲虫细长管状的雌性和雄性生殖器,称为精囊管和鞭毛的渗透。我们的研究结果表明,这种看似直接的渗透机制是由生殖器的结构和材料特殊化所支撑的。我们采用基于同步加速器的微计算机断层扫描和共聚焦激光扫描显微镜(CLSM)来观察女性和男性生殖器之间的精确机械相互作用。机械测试揭示了鞭毛内的刚度梯度和性别之间相关的刚度变化。结合CLSM和低温显微技术,我们表征了鞭毛尖端的异质性物质分布;这种特化在精囊管硬化程度较高的种中表现得更为显著。结合所观察到的材料特性进行的有限元分析表明,所观察到的材料分布极大地降低了所需的穿透力,分散了鞭毛尖端的应力。这项研究揭示了女性和男性生殖器的结构和材料适应可能是共同进化的,并突出了生物力学在生殖器研究中的重要性。
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来源期刊
Journal of The Royal Society Interface
Journal of The Royal Society Interface 综合性期刊-综合性期刊
CiteScore
7.10
自引率
2.60%
发文量
234
审稿时长
2.5 months
期刊介绍: J. R. Soc. Interface welcomes articles of high quality research at the interface of the physical and life sciences. It provides a high-quality forum to publish rapidly and interact across this boundary in two main ways: J. R. Soc. Interface publishes research applying chemistry, engineering, materials science, mathematics and physics to the biological and medical sciences; it also highlights discoveries in the life sciences of relevance to the physical sciences. Both sides of the interface are considered equally and it is one of the only journals to cover this exciting new territory. J. R. Soc. Interface welcomes contributions on a diverse range of topics, including but not limited to; biocomplexity, bioengineering, bioinformatics, biomaterials, biomechanics, bionanoscience, biophysics, chemical biology, computer science (as applied to the life sciences), medical physics, synthetic biology, systems biology, theoretical biology and tissue engineering.
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