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      The Sperm Structure and Spermatogenesis of Trypophloeus klimeschi (Coleoptera: Curculionidae: Scolytinae)

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          Abstract

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          In the mating, reproduction, and phylogenetic reconstruction of various insect taxa, the morphological characteristics of the male reproductive system, spermatogenesis, and sperm ultrastructure are important. We investigated these morphological characteristics of Trypophloeus klimeschi (Coleoptera: Curculionidae: Scolytinae), which is one of the most destructive pests of Populus alba var. pyramidalis (Bunge) using light microscopy, scanning electron microscopy, and transmission electron microscopy. We also compared these morphological characteristics with that found in other Curculionidae.

          Abstract

          The male reproductive system, sperm structure, and spermatogenesis of Trypophloeus klimeschi (Coleoptera: Curculionidae: Scolytinae), which is one of the most destructive pests of Populus alba var. pyramidalis (Bunge), were investigated using light microscopy, scanning electron microscopy, and transmission electron microscopy. The male reproductive system of T. klimeschi is composed of testes, seminal vesicles, tubular accessory glands, multilobulated accessory glands, vasa deferentia, and a common ejaculatory duct. In spermatogenesis, two phenomena are apparent: The nuclear chromatin condenses into two different patterns, and an oval preacrosomal vesicle is present at the flank of the Golgi apparatus. The sperm are short, measuring 76.7 ± 1.8 μm in length, and are 508.1 ± 12.9 nm in width. The sperm are composed of a three-layer acrosomal complex, a cylindrical nucleus, two mitochondrial derivatives, a 9 + 9 + 2 axoneme, and two accessory bodies with a large “puff”-like expansion. Mature sperm are individually stored in seminal vesicles. During spermiogenesis, the similarities in the nuclear chromatin condensation characteristics of Curculioninae and Scolytinae are indicative of their close phylogenetic relationship. It appears that the preacrosomal vesicle being flanked by the Golgi apparatus is a characteristic of spermatogenesis in Curculionidae.

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          INSECT SPERM: THEIR STRUCTURE AND MORPHOGENESIS

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            WEEVILS AND PLANTS: PHYLOGENETIC VERSUS ECOLOGICAL MEDIATION OF EVOLUTION OF HOST PLANT ASSOCIATIONS IN CURCULIONINAE (COLEOPTERA: CURCULIONIDAE)

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              Weevils, weevils, weevils everywhere*

              An overview is presented of the progress made on the taxonomy, classification and phylogeny of weevils in the 250 years since the first taxonomic descriptions of weevils by Carolus Linnaeus. The number of described weevils species is calculated to be about 62 000 and the likely total number of existing species 220 000, indicating that we have described just over a quarter of the diversity of this important group of beetles and that, at current rates of discovery and description, it will take another 650 years or so to describe the rest. Within the framework of the current concept of weevil phylogeny, a brief account is given of the seven main weevil lineages (families), and of the subfamilies of the largest of them, the Curculionidae, summarising their diversity, distribution and biology and identifying the major classificatory problems remaining in each. In conjunction with the phylogenetic hypothesis of weevil relationships and their fossil record, which is briefly summarised, the evolutionary history of weevils is mapped as a sequence of key evolutionary innovations that together have led to the phenomenal diversification and success of weevils.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Biology (Basel)
                Biology (Basel)
                biology
                Biology
                MDPI
                2079-7737
                25 June 2021
                July 2021
                : 10
                : 7
                : 583
                Affiliations
                [1 ]College of Forestry, Northwest A&F University, Yangling 712100, China; sxllgaojing@ 123456nwafu.edu.cn (J.G.); wjx2017@ 123456nwafu.edu.cn (J.W.)
                [2 ]Information Institute, Tianjin Academy of Agricultural Sciences, Tianjin 300192, China; ggqun@ 123456nwafu.edu.cn
                [3 ]State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, Guangdong Key Laboratory for Innovative Development and Utilization of Forest Plant Germplasm, College of Forestry and Landscape Architecture, South China Agricultural University, Guangzhou 510642, China
                Author notes
                [* ]Correspondence: chenhui@ 123456nwsuaf.edu.cn ; Tel.: +86-29-8708-2083
                Author information
                https://orcid.org/0000-0003-1498-6280
                Article
                biology-10-00583
                10.3390/biology10070583
                8301190
                34202012
                75b3c8df-7f3d-4336-ad96-c443de2c7dd3
                © 2021 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 29 May 2021
                : 23 June 2021
                Categories
                Article

                male reproductive system,sperm ultrastructure,spermatogenesis,trypophloeus klimeschi (coleoptera: curculionidae: scolytinae)

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