15 research outputs found

    Palaeozoic giant dragonfies were hawker predators

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    The largest insects to have ever lived were the giant meganeurids of the Late Palaeozoic, ancient stem relatives of our modern dragonfies. With wingspans up to 71cm, these iconic insects have been the subject of varied documentaries on Palaeozoic life, depicting them as patrolling for prey through coal swamp forests amid giant lycopsids, and cordaites. Such reconstructions are speculative as few defnitive details of giant dragonfy biology are known. Most specimens of giant dragonfies are known from wings or isolated elements, but Meganeurites gracilipes preserves critical body structures, most notably those of the head. Here we show that it is unlikely it thrived in densely forested environments where its elongate wings would have become easily damaged. Instead, the species lived in more open habitats and possessed greatly enlarged compound eyes. These were dorsally hypertrophied, a specialization for long-distance vision above the animal in fight, a trait convergent with modern hawker dragonfies. Sturdy mandibles with acute teeth, strong spines on tibiae and tarsi, and a pronounced thoracic skewness are identical to those specializations used by dragonfies in capturing prey while in fight. The Palaeozoic Odonatoptera thus exhibited considerable morphological specializations associated with behaviours attributable to ‘hawkers’ or ‘perchers’ among extant Odonata.This work benefted from a grant of the French ‘Agence Nationale de la Recherche’ via the program ‘Investissements d’avenir’ (ANR-11-INBS-0004-RECOLNAT)JP and MP gratefully acknowledge research support from the Grant Agency of the Czech Republic No. 18-03118 SThe work of MSE was supported by US National Science Foundation grant DEB-114416

    Changes to the Fossil Record of Insects through Fifteen Years of Discovery

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    The first and last occurrences of hexapod families in the fossil record are compiled from publications up to end-2009. The major features of these data are compared with those of previous datasets (1993 and 1994). About a third of families (>400) are new to the fossil record since 1994, over half of the earlier, existing families have experienced changes in their known stratigraphic range and only about ten percent have unchanged ranges. Despite these significant additions to knowledge, the broad pattern of described richness through time remains similar, with described richness increasing steadily through geological history and a shift in dominant taxa, from Palaeoptera and Polyneoptera to Paraneoptera and Holometabola, after the Palaeozoic. However, after detrending, described richness is not well correlated with the earlier datasets, indicating significant changes in shorter-term patterns. There is reduced Palaeozoic richness, peaking at a different time, and a less pronounced Permian decline. A pronounced Triassic peak and decline is shown, and the plateau from the mid Early Cretaceous to the end of the period remains, albeit at substantially higher richness compared to earlier datasets. Origination and extinction rates are broadly similar to before, with a broad decline in both through time but episodic peaks, including end-Permian turnover. Origination more consistently exceeds extinction compared to previous datasets and exceptions are mainly in the Palaeozoic. These changes suggest that some inferences about causal mechanisms in insect macroevolution are likely to differ as well

    Paleontology of leaf beetles

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    `The rate of evolution in any large group is not uniform; there are periods of relatise stability, and periods of comparatively rapid change.' Cockerell and LeVeque, 1931 To Yenli Ych, my beloved wife, a most wonderful person! The fossil record of the Chrysomelidae can be tentatively traced back to the late Paleozoic to early Mesozoic Triassic. Mesozoic records at least 9 subfamilies, 19 genera, and 35 species, are represented by the Sagrinae, the exclusively Mesozoic Proto scelinae, Clytrinae, Cryptocephalinae, Eumolpinae, Chrysomelinae. Galerucinac, Alticinae, and Cassidinae. Cenozoic records at least 12 subfamilies- 63 % of the extant- 12! genera, and 325 species, include the same extant subfamilies as well as the Donaciinae, Zeugophorinae, Criocerinae, and Hispinae and can be frequently identified to genus, especially if preserved in amber. Quaternary records are often identified to extant species. tn total, at least t3! genera about 4 % of total extant, and 357 species < 1 % have been reported. At least, 24 genera <1 % of the extant seem to be extinct. Although reliable biological information associated with the fossil chrysomelids is very scarce, it seems that most of the modern host-plant associations were established, at least, in the late Mesozoic to early Cenozoic. As a whole, stasis seems to be the general rule of the chrysomelid fossil record. Together with other faunal elements, chrysomelids, especially donaciines, have been used as biogeographic and paleoclimatological indicators in the Holocene. I

    The Middle Triassic insect radiation revealed by isotopic age and iconic fossils from NW China

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    Oral Presentation: SSP4.3 Integration of geological and biological processes using fossils to understand the evolution of terrestrial and marine ecosystemsFollowing the end-Permian mass extinction, the Triassic represented an important period witnessing the recovery and radiation of marine and terrestrial ecosystems. Terrestrial plants and vertebrates have been widely investigated; however the insects, the most diverse organisms on earth, remain enigmatic due to the rarity of Early–Middle Triassic fossils. Here we report new fossils from a Ladinian deposit dated at ~ 238–237 Ma and a Carnian deposit in northwestern China, including the earliest definite caddisfly cases (Trichoptera) and water boatmen (Hemiptera), diverse polyphagan beetles (Coleoptera) and scorpionflies (Mecoptera). Our findings suggest that the Holometabola, comprising the majority of modern-day insect species, experienced an extraordinary diversification in the Middle Triassic and was already been dominant in some Middle and Late Triassic insect faunas, after the extinction of several ecologically dominant, Paleozoic insect groups in the latest Permian and earliest Triassic. This turnover is perhaps related to notable episodes of extreme warming and drying, leading to the eventual demise of coal-swamp ecosystems, evidenced by floral turnover during this interval. The forest revival during the Middle Triassic probably stimulated the rapid radiation and evolution of insects including some key aquatic lineages which built new associations that persist to the present day. Our results provide not only new insights into the early evolution of insect diversity and ecology, but also robust evidence for the view that the Triassic is the 'Dawn of the Modern World'. Besides, LA-ICP-MS U-Pb dating initially gave a late Ladinian age for the Tongchuan entomnfauna after the results: 237.41 0.91 Ma and 238 0.97 Ma. The age is in agreement with that of the marine Ladinian-Carnian boundary, representing a novel age constraint for the terrestrial strata near this boundary. This age can provide a calibration for marine and terrestrial correlation near Ladinian-Carnian boundary, and also for the correlation of the contemporaneous biotas
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