Tracheal hyperallometry and spatial constraints in a large beetle

IF 2.3 2区 农林科学 Q1 ENTOMOLOGY
Tomer Urca , Gal Ribak , Eran Gefen
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Abstract

Insects exchange respiratory gases with their environment through their gas-filled tracheal system, a branched tracheal tree extending from segmental openings and terminating at fine tissue penetrating tracheoles. It was shown that the tracheal volume increases hyperallometrically with insect body size (Mb), both interspecifically and across developmental stages. In this study, we used the sixfold Mb variation in adult Batocera rufomaculata (Cerambicidae; Coleoptera) examining the allometry of adult tracheal volume (Vtr). We further explored the effect of sex and sexual maturity on tracheal gas conductance, testing the hypotheses that (i) larger body size and (ii) egg volume in gravid females would result in lower safety margins for tracheal oxygen transport due to structural restriction. We report a hyperallometric tracheal growth in both sexes of adult B. rufomaculata (mean mass exponent of 1.42 ± 0.09), similar in magnitude to previously reported values. Tracheal gas conductance was independent of Mb and reproductive state, but was significantly higher in females compared with males. We suggest that females may have pre-adapted a higher tracheal conductance required for the higher flight power output while gravid. Lack of compliant air sacs and rigid trachea may explain how gravid females retain their Vtr. However, we show that Vtr outgrows thoracic dimensions with increased B. rufomaculata size. Hyperallometric growth of the giant cerambycid thoracic trachea could explain the previously reported hypometric scaling of flight muscles in B. rufomaculata, and the compromised long-distance flight performance of larger compared with smaller conspecifics.

大型甲虫的气管超量测定和空间限制。
昆虫通过充满气体的气管系统与周围环境交换呼吸气体,气管系统是一个从节间开口延伸到细小组织穿透气管孔的分支气管树。研究表明,气管体积随着昆虫体型(Mb)的增大而增大,在不同物种间和不同发育阶段都是如此。在本研究中,我们利用成虫 Batocera rufomaculata(蠰科;鞘翅目)的六倍 Mb 差异研究了成虫气管体积(Vtr)的异方差。我们进一步探讨了性别和性成熟对气管气体传导的影响,并检验了以下假设:(i) 体型较大;(ii) 怀卵雌虫的卵体积会因结构限制而导致气管氧气输送的安全系数降低。我们报告了雌雄成虫气管的超测速增长(平均质量指数为 1.42 ± 0.09),与之前报告的数值相近。气管气体传导率与 Mb 和繁殖状态无关,但雌性明显高于雄性。我们认为,雌性可能已经预先适应了较高的气管导气率,以便在怀孕期间输出较高的飞行动力。缺乏顺应性气囊和僵硬的气管也许可以解释雌鸟如何保持其 Vtr。然而,我们的研究表明,随着红腹滨蝽体型的增大,Vtr会超过胸廓尺寸。巨角雉胸腔气管的超几何增长可以解释之前报道的巨角雉飞行肌肉的超几何缩放,以及与较小的同种鸟相比,体型较大的巨角雉远距离飞行性能下降的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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