Matsumura Yoko, Michels Jan, Appel Esther, Gorb Stanislav N
Department of Functional Morphology and Biomechanics, Zoological Institute, Kiel University, Am Botanischen Garten 1-9, D-24118 Kiel, Germany; Department of Biology, Keio University, 4-1-1 Hiyoshi, Yokohama 223-8521, Japan.
Department of Functional Morphology and Biomechanics, Zoological Institute, Kiel University, Am Botanischen Garten 1-9, D-24118 Kiel, Germany.
Zoology (Jena). 2017 Feb;120:1-14. doi: 10.1016/j.zool.2016.08.001. Epub 2016 Aug 8.
The peculiar phenomenon of hyper-elongation of intromittent organs is well known in a number of insect groups. However, the unresolved questions of how and why such a phenomenon originated independently many times continue to attract biologists' attention. To be able to detect the evolutionary driving mechanisms that enabled insects to repeatedly acquire such a peculiarity, first of all the structural key features and the mechanics of these organs have to be determined. In the present study, the morphology of the reproductive organs of two species of the beetle genus Cassida, with a special focus on the male structures, was scrutinised in detail during copulation and at rest using different microscopy techniques. We found that the hyper-elongated structure of the intromittent organ, called flagellum, is part of the male ejaculatory duct. When the flagellum is inserted into the female spermathecal duct, longitudinal muscles of the ejaculatory duct, but not the flagellum, are shortened. These results strongly suggest that the contraction of the longitudinal muscles of the ejaculatory duct causes propulsion of the flagellum into the highly spiralled spermathecal duct of the female. The tip of the cuticular flagellum is curled up, which can suggest that its physical properties differ from those of the rest of the flagellum. Considering the preceding modelling studies, this property aids the flagellum in penetrating within the highly spiralled and very variable female duct. Based on our morphological results and in comparison with the morphology of intromittent organs of other beetles, we discuss the evolutionary origin of the hyper-elongation in the Cassida species and propose a hypothesis that explains the independent origin of the hyper-elongation of intromittent organs.
在许多昆虫类群中,交配器官超伸长的奇特现象广为人知。然而,这种现象如何以及为何多次独立起源的未解问题,依然吸引着生物学家的关注。为了能够探寻使昆虫反复获得这种特性的进化驱动机制,首先必须确定这些器官的结构关键特征及其力学原理。在本研究中,利用不同的显微镜技术,对叶甲属两种甲虫的生殖器官形态进行了详细检查,特别关注雄性结构,包括交配时和静止时的情况。我们发现,交配器官的超伸长结构——鞭状体,是雄性射精管的一部分。当鞭状体插入雌性交配囊导管时,射精管的纵向肌肉而非鞭状体缩短。这些结果有力地表明,射精管纵向肌肉的收缩促使鞭状体推进到雌性高度螺旋状的交配囊导管中。角质化鞭状体的尖端卷曲,这可能表明其物理特性与鞭状体的其他部分不同。结合之前的模型研究,这种特性有助于鞭状体穿透高度螺旋且变化多样的雌性导管。基于我们的形态学研究结果,并与其他甲虫交配器官的形态进行比较,我们讨论了叶甲属物种中超伸长现象的进化起源,并提出了一个假说,用以解释交配器官超伸长的独立起源。