29 research outputs found

    YET ANOTHER UNUSUAL NEW TYPE OF LACEWING LARVA PRESERVED IN 100-MILLION-YEAR OLD AMBER FROM MYANMAR

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    Lacewing larvae are mostly predatory, highly mobile larval forms of Insecta. The modern fauna yields several morphotypes of lacewing larvae, each closely associated with a distinct evolutionary lineage within the group of lacewings, Neuroptera. Back in the Cretaceous, about 100 million years ago, many of these larval forms had already evolved. Additionally, many larval forms seem to have been present that are now extinct. We report here a new form, which appears to be extinct now. This new larva has a prominent forward projecting labrum like larval forms of Nevrorthidae and Psychopsidae. It furthermore has (again similar to the latter two) curved venom-injecting stylets formed by mandibles and maxillae. We used quantitative outline analysis to compare the new larva to those of Nevrorthidae and Psychopsidae. The results of this analysis demonstrate that the new larva differs in all aspects of head capsule shape from all known larvae of Nevrorthidae. Its head shape is more similar to that of many larvae of Psychopsidae, yet also here the new larva differs recognisably in one principal component. Also qualitative differences clearly differentiate the new larva from already known ones. Hence, the new larva represents a new, so far unknown morphotype of lacewing larva. This finding adds to the growing 'zoo' of unusual lacewing larvae back in the Cretaceous, indicating that form diversity and ecological diversity of lacewings were much higher 100 million years ago

    Declining morphological diversity in snakefly larvae during last 100 million years

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    Raphidioptera, the group of snakeflies, is a rather species-poor in-group of Holometabola. Yet, fossils of snakeflies indicate that the group was more diverse in the past. Here we compare the morphological diversity of snakefly larvae over time. Snakefly larvae are well represented in Cretaceous and Eocene ambers facilitating such a comparison. We used measurements of discrete dimensions as a basis for comparison. This reveals a larger diversity of snakefly larvae in the Cretaceous, especially in relation to head shapes and morphology of the antennae, which were much more variable. In particular, some Cretaceous larvae possessed greatly elongated head capsules and uniquely long and prominent antennae, unparalleled among modern forms. Already by the Eocene, snakefly larvae were less variable than those of the Cretaceous, although some still possessed longer antennae than modern-day larvae. The loss of morphological diversity supports the already well-established loss of taxonomic diversity in the group across time. Quite likely, this also indicates a loss of ecological diversity. These results are comparable to losses in different lineages of the closely related group Neuroptera

    The Diversity of Aphidlion-like Larvae over the Last 130 Million Years

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    Aphidlions are larvae of certain lacewings (Neuroptera), and more precisely larvae of the groups Chrysopidae, green lacewings, and Hemerobiidae, brown lacewings. The name ‘aphidlion’ originates from their ecological function as specialised predators of aphids. Accordingly, they also play an economic role as biological pest control. Aphidlions have, mostly, elongated spindle-shaped bodies, and similarly to most lacewing larvae they are equipped with a pair of venom-injecting stylets. Fossils interpreted as aphidlions are known to be preserved in amber from the Cretaceous (130 and 100 million years ago), the Eocene (about 35 million years ago) and the Miocene (about 15 million years ago) ages. In this study, new aphidlion-like larvae are reported from Cretaceous amber from Myanmar (about 100 million years old) and Eocene Baltic amber. The shapes of head and stylets were compared between the different time slices. With the newly described fossils and specimens from the literature, a total of 361 specimens could be included in the analysis: 70 specimens from the Cretaceous, 5 from the Eocene, 3 from the Miocene, 188 extant larvae of Chrysopidae, and 95 extant larvae of Hemerobiidae. The results indicate that the diversity of head shapes remains largely unchanged over time, yet there is a certain increase in the diversity of head shapes in the larvae of Hemerobiidae. In certain other groups of Neuroptera, a distinct decrease in the diversity of head shapes in larval stages was observed

    NEW FOSSIL LACEWING LARVAE WITH TRUMPET-SHAPED ELONGATE EMPODIA PROVIDE INSIGHT INTO THE EVOLUTION OF THIS ATTACHMENT STRUCTURE

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    The larval life phase often represents the major share of the life span of holometabolans, such as beetles or flies. Therefore, knowledge of these larvae is crucial concerning ecological functions, but also concerning the evolutionary history of the different groups. In the holometabolan group Neuroptera (lacewings), larvae have numerous specialisations, among them the venom-injecting mouthparts, the stylets. Another such very characteristic feature of many lacewing larvae is the empodium, an attachment structure at the tip of the leg, which varies in shape in the larvae of the different lacewing groups. One type of empodium is the elongate trumpet-shaped type, which is found in several lacewing groups today as well as in many fossil representatives, especially well visible due to preservation in amber. Based on the pattern of phylogenetic distribution of the elongate trumpet-shaped empodium, different reconstructions of the evolution of this structure have been put forward, some suggesting possibly convergent evolution, others repetitive losses. In this study, new lacewing larvae preserved in 100-million-year-old amber from Myanmar are presented, which expand the number of lineages with an elongate trumpet-shaped empodium. Based on these new data, the implications on the evolutionary history of the different lineages within Neuroptera are discussed. The fossils demand for an earlier evolution in some reconstructions, but especially for more and later losses of this structure

    Measurement of the W boson polarisation in ttˉt\bar{t} events from pp collisions at s\sqrt{s} = 8 TeV in the lepton + jets channel with ATLAS

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    Measurement of jet fragmentation in Pb+Pb and pppp collisions at sNN=2.76\sqrt{{s_\mathrm{NN}}} = 2.76 TeV with the ATLAS detector at the LHC

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    Search for new phenomena in events containing a same-flavour opposite-sign dilepton pair, jets, and large missing transverse momentum in s=\sqrt{s}= 13 pppp collisions with the ATLAS detector

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    Measurements of top-quark pair differential cross-sections in the eμe\mu channel in pppp collisions at s=13\sqrt{s} = 13 TeV using the ATLAS detector

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    Search for dark matter in association with a Higgs boson decaying to bb-quarks in pppp collisions at s=13\sqrt s=13 TeV with the ATLAS detector

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