The name Anser scaldii was first used by Van Beneden (1872) in a brief text that read ‘Nous avons recu un humérus dans un parfait état de conservation, trouvé dans le crag, à Anvers’. The name was also used by Van Beneden (1873), but in both instances it is a nomen nudum. The name was made valid for the purposes of nomenclature by Lambrecht (1933: 368) when he entered Anser scaldii Van Beneden, 1872, with the following description and information: ‘Humerus typisch anserin, von der Größe von Tadorna casarca. Länge 129 mm. Material: Humerus im Mus. Bruxelles. Alter und Fundort: Obermiozän (Bolderian), Antwerpen. Etymologie: Artname nach der Schelde: Scaldia.’ At the same time he mistakenly gave the original combination as Anas scaldii Van Beneden 1872, which error was perpetuated by Gaillard (1939), Brodkorb (1964), Howard (1964), and Bochenski (1997), as noted by Mlíkovský (2002: 125). The statement by Lambrecht that this fossil is of similar length to humeri of Tadorna prompted Worthy et al. (2007) to suggest that Anser scaldii may have a bearing on the evolution of Tadornini in Europe. Accordingly, we re- examined the holotype in the Department of Paleontology, Royal Belgian Institute of Natural Sciences, Brussels, Belgium, to ascertain its relationships and its significance in Anseriform evolution.
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Platycampus larvae are highly cryptic leaf feeders characterised by a dorso-ventrally flattened body, the dorsal integument resembling a shield. Dorsal and ventral cuticles from Platycampus luridiventris were compared by histology and gel electrophoresis. By Azan-staining, a red and a blue layer were distinguished in the dorsal cuticle, while the ventral cuticle showed one, almost uniform blue layer, as in both cuticles of control species. The two cuticles from P. luridiventris had similar amounts and sodium dodecyl sulphate-polyacrylamide gel electrophoresis profiles of soluble proteins, but not insoluble proteins. One insoluble protein (MW approximately 41 kDa) was visible as a large band in the ventral cuticle only. It is likely that this protein renders the cuticle elastic, and that the dorsal, red layer is the exocuticle, mainly composed of insoluble proteins. We discuss eco-physiological implications of the exocuticle in insects. Further, data from the literature indicate that the defence strategy in P. luridiventris larvae relies on being visually cryptic towards avian predators and tactically cryptic towards arthropod predators and parasitoids. Crypsis in both senses is favoured by the shield effect, itself based on an abnormally thick dorsal exocuticle. Although the larvae are external feeders, they may be considered as hidden from an ecological perspective.
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