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      Fossil dragonfly-type larva with lateral abdominal protrusions and implications on the early evolution of Pterygota

      research-article
      1 , 2 , 3 , 1 , 2 , 4 ,
      iScience
      Elsevier
      Paleontology, Entomology, Evolutionary history, Paleobiology

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          Summary

          Aquatic larvae are known in three early branches of Pterygota: Ephemeroptera (mayflies), Plecoptera (stoneflies), and Odonata (dragonflies, damselflies). A common origin of these larvae has been suggested, yet also counterarguments have been put forward, for example, the different position of larval gills: laterally on the abdomen in Ephemeroptera, terminally in Odonata, variably in Plecoptera. We discuss recent fossil findings and report a new dragonfly-type larva from Kachin amber (Myanmar), which possesses ancestral characters such as a terminal filum, maintained in ephemeropterans, but lost in modern odonatan larvae. The new larva possesses lateral protrusions on the abdominal segments where in other lineages gills occur. Together with other fossils, such as a plecopteran retaining lateral gills on the abdomen, this indicates that lateral protrusions on the abdomen might have well been an ancestral feature, removing one important argument against the idea of an aquatic larva in the ground pattern of Pterygota.

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          Highlights

          • A new dragonfly-type larva was found in Kachin amber (Myanmar, 99 million years old).

          • The larva possesses a terminal filum, which is not known in modern dragonfly larvae

          • It also exhibits lateral abdominal protrusions where in other lineages gills occur

          • This find makes an aquatic larva in the ground pattern of Pterygota more likely

          Abstract

          Paleontology; Entomology; Evolutionary history; Paleobiology

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          Most cited references34

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          Deep homology and the origins of evolutionary novelty.

          Do new anatomical structures arise de novo, or do they evolve from pre-existing structures? Advances in developmental genetics, palaeontology and evolutionary developmental biology have recently shed light on the origins of some of the structures that most intrigued Charles Darwin, including animal eyes, tetrapod limbs and giant beetle horns. In each case, structures arose by the modification of pre-existing genetic regulatory circuits established in early metazoans. The deep homology of generative processes and cell-type specification mechanisms in animal development has provided the foundation for the independent evolution of a great variety of structures.
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            Age constraint on Burmese amber based on U–Pb dating of zircons

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              Repeated morphological evolution through cis-regulatory changes in a pleiotropic gene.

              The independent evolution of morphological similarities is widespread. For simple traits, such as overall body colour, repeated transitions by means of mutations in the same gene may be common. However, for more complex traits, the possible genetic paths may be more numerous; the molecular mechanisms underlying their independent origins and the extent to which they are constrained to follow certain genetic paths are largely unknown. Here we show that a male wing pigmentation pattern involved in courtship display has been gained and lost multiple times in a Drosophila clade. Each of the cases we have analysed (two gains and two losses) involved regulatory changes at the pleiotropic pigmentation gene yellow. Losses involved the parallel inactivation of the same cis-regulatory element (CRE), with changes at a few nucleotides sufficient to account for the functional divergence of one element between two sibling species. Surprisingly, two independent gains of wing spots resulted from the co-option of distinct ancestral CREs. These results demonstrate how the functional diversification of the modular CREs of pleiotropic genes contributes to evolutionary novelty and the independent evolution of morphological similarities.
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                Author and article information

                Contributors
                Journal
                iScience
                iScience
                iScience
                Elsevier
                2589-0042
                24 September 2021
                22 October 2021
                24 September 2021
                : 24
                : 10
                : 103162
                Affiliations
                [1 ]Ludwig-Maximilians-Universität München (LMU Munich), Biocenter, Großhaderner Str. 2, 82152 Planegg-Martinsried, Germany
                [2 ]GeoBio-Center at LMU, Richard-Wagner-Str. 10, 80333 München, Germany
                [3 ]Kreuzbergstr. 90, 66482 Zweibrücken, Germany
                Author notes
                []Corresponding author carolin.haug@ 123456palaeo-evo-devo.info
                [4]

                Lead contact

                Article
                S2589-0042(21)01130-5 103162
                10.1016/j.isci.2021.103162
                8501664
                34646993
                3bd424a9-e366-4109-a998-de82610375cc
                © 2021 The Author(s)

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 20 June 2021
                : 23 July 2021
                : 20 September 2021
                Categories
                Article

                paleontology,entomology,evolutionary history,paleobiology

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