新热带蝈蝈(Conocephalus ictus)(直翅目 Tettigoniidae)新婚礼物蛋白质的潜在战略分配。

IF 2.3 2区 农林科学 Q1 ENTOMOLOGY
Raúl Cueva del Castillo, Anahi Elias-Quevedo, Josefina Vázquez Medrano, Anabel Ruíz-Flores, César M. Flores-Ortiz
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引用次数: 0

摘要

在许多螽斯中,雄性会用大的凝胶状精囊喂养配偶。虽然提供大的精囊可以提高雌性的繁殖力和寿命,但也可能降低雌性的性接受能力,从而有利于雄性的健康。将资源分配给这些可食用的礼物可能会降低其他功能的分配,从而在躯体功能和生殖功能之间产生权衡。尽管精子对雄性和雌性的体能都有影响,但人们对与螽斯精囊有关的化合物知之甚少。我们的研究发现,Conocephalus ictus 的精囊中有 177 种不同的推定蛋白质,雄性体型与精囊质量、蛋白质数量、浓度和质量之间没有相关性。然而,我们确实观察到雄性前翅长度与蛋白质浓度之间存在负相关关系,转移到雌性体内的精子质量与雌性体型之间存在负相关关系,这表明雄性体内存在资源分配权衡,同时也存在基于雌性质量的资源战略转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Potential strategic allocation of nuptial gift proteins of the neotropical katydid Conocephalus ictus (Orthoptera Tettigoniidae)

Potential strategic allocation of nuptial gift proteins of the neotropical katydid Conocephalus ictus (Orthoptera Tettigoniidae)

In many katydids, the male feeds his mate with a large gelatinous spermatophore. While providing large spermatophores can increase female fecundity and lifespan, it may also decrease their sexual receptivity, benefiting male fitness. Allocating resources to these edible gifts may entail a lower apportionment of them to other functions, generating a trade-off between somatic and reproductive functions. Despite their effect on male and female fitness, little is known of the compounds associated with katydid spermatophores. Our study found 177 different putative proteins in the spermatophore of Conocephalus ictus, with no correlation between male body size with spermatophore mass, number, concentration and mass of proteins. However, we did observe a negative relationship between male forewing length and protein concentration, and a negative relationship between the mass of the spermatophore transferred to the females and their body size, suggesting a resource allocation trade-off in males, but also strategic transference of resources based on female quality.

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来源期刊
Journal of insect physiology
Journal of insect physiology 生物-昆虫学
CiteScore
4.50
自引率
4.50%
发文量
77
审稿时长
57 days
期刊介绍: All aspects of insect physiology are published in this journal which will also accept papers on the physiology of other arthropods, if the referees consider the work to be of general interest. The coverage includes endocrinology (in relation to moulting, reproduction and metabolism), pheromones, neurobiology (cellular, integrative and developmental), physiological pharmacology, nutrition (food selection, digestion and absorption), homeostasis, excretion, reproduction and behaviour. Papers covering functional genomics and molecular approaches to physiological problems will also be included. Communications on structure and applied entomology can be published if the subject matter has an explicit bearing on the physiology of arthropods. Review articles and novel method papers are also welcomed.
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