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- Abdominal appendages (1)
- Adult insects (1)
- Bauplan (1)
- CT (1)
- Dicondylia (1)
- Grylloblattodea (1)
- X-ray computed tomography (1)
Despite their enormous diversity, the bauplan of adult winged insects (pterygotes) is remarkably conservative since the Lower Devonian: a five-segmented head, a three-segmented thorax with three pairs of walking legs and an eleven-segmented abdomen without any non-sexual appendages 1 and 2. The only known exceptions are the abdominal appendages of adult male sepsid flies on the fourth segment; however, these are also used as copulatory organs and are supposedly maintained through sexual selection [3]. Here, we report a rod-like paired appendage from the third and fourth abdominal segments in adults of the Southeast-Asian Hemiptera taxon Bennini (Figure 1A,B; Supplemental information). These are fully musculated, innervated, and movable and bear highly organized sensory and secretory units. The appendages, termed LASSO (lateral abdominal sensory and secretory organs), are consistent in topology and structure in all species studied and not sexually dimorphic. The existence of these non-sexual abdominal appendages reveals the potential of the 300 million year old conserved bauplan of insects.
External and internal head structures of adults of Galloisiana yuasai (Grylloblattodea) are described. The results are compared with conditions found in representatives of other lower neopteran lineages, notably in Austrophasma and Karoophasma (both Mantophasmatodea). Sutures and ridges of the head capsule are discussed. A new nomenclature for head muscles is presented for the entire Dicondylia (= Zygentoma + Pterygota). Galloisiana (like its sister taxon Grylloblatta) is mostly characterized by plesiomorphic features, such as the largely unspecialized orthopteroid mouthparts, the multisegmented filiform antennae, the presence of trabeculae tentorii, the absence of muscles associated with the antennal ampullae, the presence of musculus stipitalis transversalis (0mx11) and the presence of musculus tentoriofrontalis anterior (0te2). Autapomorphies of Grylloblattodea are: (i) compound eyes composed of only 60 ommatidia or less; (ii) a lacinia with a proximal tooth; (iii) a rounded submentum; (iv) loss of musculus craniohypopharyngealis (0hy3); and (v) loss of musculus labroepipharyngealis (0lb5). The phylogenetic evaluation of 104 characters of the head yields a branching pattern with Grylloblattodea as a sister group of Mantophasmatodea in clade Xenonomia. Putative synapomorphies of both taxa are: (i) a distinct angle (more than 60°) between the submentum and the mentum; (ii) posteriorly oriented labial palpi; (iii) a flat and lobe-like hypopharynx with a suspensorium far ventrad of the anatomical mouth opening; (iv) loss of musculus tentorioparaglossalis (0la6); and (v) a connection between the antennal ampulla and the supraoesophageal ganglion containing nuclei. Xenonomia is placed in a clade with the two dictyopteran terminals. Another monophyletic group is Embioptera + Phasmatodea. Most branches of the single tree obtained in our analysis are weakly supported. The results clearly show that more data and a much broader taxon sampling are required to clarify the phylogenetic interrelationships of the lower neopteran orders. However, our results narrow down the spectrum of possible solutions, and represent a starting point for future phylogenetic analyses, with an extensive concatenated dataset.