Abstract

BackgroundInsemination in scorpions is carried out by means of a partly sclerotized structure, the spermatophore, which is composed of two separate halves, the hemispermatophores. In most genera these reproductive structures can be used to differentiate species. However, many taxa such as the genus Euscorpius and the family Diplocentridae lack the morphological diversity observed in the copulatory organs of many other arthropods, rendering them useless for species level taxonomy. Such structural stasis, however, suggests that hemispermatophores have evolved relatively slowly and may thus provide a stronger phylogenetic signal for recognizing supra-generic ranks than previously thought. Based on the postulate that the phenotypic stability observed in some groups is the consequence of functional constraint, the most comprehensive comparative study of the male sexual apparatus to date was conducted for a complete reassessment of the morphology, phylogenetic value and hypotheses of homology of these structures.ResultsHemispermatophores, pre- and post-insemination spermatophores, as well as the inherent mechanisms of insemination, were studied across the whole order, allowing the recognition and description of a series of five basic bauplans for the capsular region. For the most part, these patterns appear to be consistent within each major taxonomic group, but several cases of incongruence between spermatophore morphology and taxonomy raises questions about the monophyly of some clades. The Bothriuridae are traditionally regarded as a basal scorpionoid family. However, except for the genus Lisposoma, bothriurid hemispermatophores and spermatophores are morphologically more similar to those of the Chactoidea than to those of scorpionoids. On the other hand, the male copulatory structures of the hormurid clade (Hormiops (Hormurus + Liocheles)) are more akin to those of Diplocentridae and Heteroscorpionidae than to those of other hormurids.ConclusionsSpermatophore capsular patterns appears to be congruent with a recent phylogeny of the order Scorpiones based on phylogenomic data that placed Bothriuridae outside of Scorpionoidea and Liocheles outside of Hormuridae, in contradicton with earlier phylogenetic reconstructions based on morphology. This raises questions about the potential use of functionally constrained traits to assess the reliability of contradicting phylogenetic hypotheses and emphasizes the need for a thorough reassessment of the scorpion phylogenetic relationships.

Highlights

  • Insemination in scorpions is carried out by means of a partly sclerotized structure, the spermatophore, which is composed of two separate halves, the hemispermatophores

  • Morphology of the scorpion reproductive apparatus In scorpions, sperm is not transferred directly by a sexual organ, but using a spermatophore, an external, partly sclerotized structure containing the spermatozoa, which is produced and deposited on the ground by the male [1]. This spermatophore is composed of two halves, the hemispermatophores, which are secreted by the paraxial organs [2] and joined together when they are expelled from the body during courtship

  • Their shapes and proportions can be extremely variable, each part has the same function in all taxa: (1) the pedicel is used to glue the spermatophore to the substrate, (2) the stem is composed of soft membranes and contains the spermatozoa, (3) the stalk (= flagellum and distal lamina sensu Lamoral [3]) is usually sclerotized and acts as a lever to trigger the compression of the stem in most taxa, and (4) the capsule is located between the stem and the stalk and guides semen from the spermatophore cavity to the female genital tract

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Summary

Introduction

Insemination in scorpions is carried out by means of a partly sclerotized structure, the spermatophore, which is composed of two separate halves, the hemispermatophores. The spermatophore is composed of four distinct parts (Fig. 1) Their shapes and proportions can be extremely variable, each part has the same function in all taxa: (1) the pedicel is used to glue the spermatophore to the substrate, (2) the stem is composed of soft membranes and contains the spermatozoa, (3) the stalk (= flagellum and distal lamina sensu Lamoral [3]) is usually sclerotized and acts as a lever to trigger the compression of the stem in most taxa, and (4) the capsule is located between the stem and the stalk and guides semen from the spermatophore cavity to the female genital tract. The capsule shows the greatest structural variation in the spermatophore, ranging from simple openings to complex eversible structures

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