The appearance of wings in insects, early in their evolution [1], has been one of the more critical innovations contributing to their extraordinary diversity. Despite the conspicuousness and importance of wings, the origin of these structures has been difficult to resolve and represented one of the "abominable mysteries" in evolutionary biology [2]. More than a century of debate has boiled the matter down to two competing alternatives-one of wings representing an extension of the thoracic notum, the other stating that they are appendicular derivations from the lateral body wall. Recently, a dual model has been supported by genomic and developmental data [3-6], representing an amalgamation of elements from both the notal and pleural hypotheses. Here, we reveal crucial information from the wing pad joints of Carboniferous palaeodictyopteran insect nymphs using classical and high-tech techniques. These nymphs had three pairs of wing pads that were medially articulated to the thorax but also broadly contiguous with the notum anteriorly and posteriorly (details unobservable in modern insects), supporting their overall origin from the thoracic notum as well as the expected medial, pleural series of axillary sclerites. Our study provides support for the formation of the insect wing from the thoracic notum as well as the already known pleural elements of the arthropodan leg. These results support the unique, dual model for insect wing origins and the convergent reduction of notal fusion in more derived clades, presumably due to wing rotation during development, and they help to bring resolution to this long-standing debate.
Antarctica, with its severe conditions, is poor in terrestrial fauna species. However, an increase in human presence together with climate change may cause an influx of non-native species. Here we report a significant increase in colonized area of one of the few known invasive species to date in Antarctica. Non-native flies of Trichocera maculipennis have been recently observed in the Admiralty Bay area on King George Island, South Shetlands Islands, West Antarctica, 10 years after its first record in Maritime Antarctica (Maxwell Bay, King George Island). Its rapid spread across the island, despite geographic barriers such as glaciers, indicates successful adaptation to local environmental conditions and suggests this species is invasive. The mode of life of T. maculipennis, observed in natural and anthropogenous habitat and in laboratory conditions, is reported. The following adaptations enabled its invasion and existence within the sewage system in Antarctic scientific stations: the ability to survive in complete darkness, male ability to mate on the substrate surface without prior swarming in flight, and adaptation of terrestrial larvae to survive in semi-liquid food. Possible routes of introduction to Antarctica and between two bays on King George Island are discussed, as well as further research leading to the containment and eradication of this species.
The Late Palaeozoic insect superorder Palaeodictyopterida exhibits a remarkable disparity of larval ecomorphotypes, enabling these animals to occupy diverse ecological niches. The widely accepted hypothesis presumed that their immature stages only occupied terrestrial habitats, although authors more than a century ago hypothesized they had specializations for amphibious or even aquatic life histories. Here, we show that different species had a disparity of semiaquatic or aquatic specializations in larvae and even the supposed retention of abdominal tracheal gills by some adults. While a majority of mature larvae in Palaeodictyoptera lack unambiguous lateral tracheal gills, some recently discovered early instars had terminal appendages with prominent lateral lamellae like in living damselflies, allowing support in locomotion along with respiratory function. These results demonstrate that some species of Palaeodictyopterida had aquatic or semiaquatic larvae during at least a brief period of their post-embryonic development. The retention of functional gills or gill sockets by adults indicates their amphibious lifestyle and habitats tightly connected with a water environment as is analogously known for some modern Ephemeroptera or Plecoptera. Our study refutes an entirely terrestrial lifestyle for all representatives of the early diverging pterygote group of Palaeodictyopterida, a greatly varied and diverse lineage which probably encompassed many different biologies and life histories.
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