Development and reproductive biology of Dermaptera: a comparative study of thirteen species from eight families

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Abstract

Abstract We examine and describe the embryonic development of 13 species from eight families of Dermaptera, i.e., all families excluding Karschiellidae, Hemimeridae, and Arixeniidae: Diplatys flavicollis (Diplatyidae), Cranopygia sp., Echinosoma sp., and Parapsalis infernalis (Pygidicranidae), Apachyus chartaceus (Apachyidae), Anisolabis maritima and Euborellia pallipes (Anisolabididae), Labidura riparia (Labiduridae), Forficula scudderi and Anechura harmandi (Forficulidae), Paralabella curvicauda (Spongiphoridae), and Proreus simulans and chelisochid gen. sp. (Chelisochidae). We also provide new findings on the reproductive biology of the Pygidicranidae and the postembryonic development of the Apachyidae. Based on information from the present and previous studies, we reconstruct the developmental and reproductive-biological groundplan for Dermaptera and discuss phylogenetic issues related to this order. We confirmed that Dermaptera possesses the embryological features (related to mode of embryonic formation and manner of blastokinesis) that are regarded as autapomorphies of Polyneoptera. Eudermaptera is characterized by the extraordinarily great length of the embryo which attains its maximum length in anatrepsis period, the positioning of its posterior end at the egg’s anterior ventral side, the type of egg tooth, and four larval instars. Anisolabididae, Labiduridae, and Eudermaptera share an elongation ratio of embryos in the anatrepsis period (ERE) of 160% or less and a larval instar number of five or less, whereas Protodermaptera is characterized by an ERE of 210% or more, a ratio of embryonic primordium relative to the egg’s longitudinal circumference (IL) of 40% or less, and a larval instar number of six or more. Notably, the ERE, IL, and larval instar number of Apachyidae are within the ranges observed in Protodermaptera.

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Phylogenomics resolves the timing and pattern of insect evolution.

Bernhard Misof, Shanlin Liu, Karen Meusemann … (2014)

Insects are the most speciose group of animals, but the phylogenetic relationships of many major lineages remain unresolved. We inferred the phylogeny of insects from 1478 protein-coding genes. Phylogenomic analyses of nucleotide and amino acid sequences, with site-specific nucleotide or domain-specific amino acid substitution models, produced statistically robust and congruent results resolving previously controversial phylogenetic relations hips. We dated the origin of insects to the Early Ordovician [~479 million years ago (Ma)], of insect flight to the Early Devonian (~406 Ma), of major extant lineages to the Mississippian (~345 Ma), and the major diversification of holometabolous insects to the Early Cretaceous. Our phylogenomic study provides a comprehensive reliable scaffold for future comparative analyses of evolutionary innovations among insects. Copyright © 2014, American Association for the Advancement of Science.

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Evolutionary history of Polyneoptera and its implications for our understanding of early winged insects

Benjamin Wipfler, Harald Letsch, Paul Frandsen … (2019)

Polyneoptera represents one of the major lineages of winged insects, comprising around 40,000 extant species in 10 traditional orders, including grasshoppers, roaches, and stoneflies. Many important aspects of polyneopteran evolution, such as their phylogenetic relationships, changes in their external appearance, their habitat preferences, and social behavior, are unresolved and are a major enigma in entomology. These ambiguities also have direct consequences for our understanding of the evolution of winged insects in general; for example, with respect to the ancestral habitats of adults and juveniles. We addressed these issues with a large-scale phylogenomic analysis and used the reconstructed phylogenetic relationships to trace the evolution of 112 characters associated with the external appearance and the lifestyle of winged insects. Our inferences suggest that the last common ancestors of Polyneoptera and of the winged insects were terrestrial throughout their lives, implying that wings did not evolve in an aquatic environment. The appearance of the first polyneopteran insect was mainly characterized by ancestral traits such as long segmented abdominal appendages and biting mouthparts held below the head capsule. This ancestor lived in association with the ground, which led to various specializations including hardened forewings and unique tarsal attachment structures. However, within Polyneoptera, several groups switched separately to a life on plants. In contrast to a previous hypothesis, we found that social behavior was not part of the polyneopteran ground plan. In other traits, such as the biting mouthparts, Polyneoptera shows a high degree of evolutionary conservatism unique among the major lineages of winged insects.