The Lamprima stag beetles have a very complex taxonomic history with > 30 synonyms in use across the genus at various times. This history is explained by poor taxonomy which typically focussed on variation in trivial features such as colour, size, body proportions and surface sculpture (Reid, et al. 2018). A recent taxonomic revision of Lamprima recognises five species: one in New Guinea (L. adolphinae Gestro, 1875), two on isolated western Pacific islands (L. aenea Fabricius, 1792: Norfolk Island; L. insularis W.J.Macleay, 1885: Lord Howe Island), one in north eastern New South Wales (L. imberbis Carter, 1926) and a common widespread species in eastern and southern Australia (L. aurata Latreille, 1817) (Reid, et al 2018). Lamprima aurata is widespread in coastal and near coastal mainland Australia from Cooktown in northern Queensland to the southern coast of Victoria and west from the Lakes Entrance, Victoria to Geraldton in Western Australia (Reid, et al 2018). Lamprima aurata is common and widespread in eastern and coastal Tasmania including the larger Bass Strait islands (Fearn 1996; Reid, et al 2018). Life histories and ecology appear to be analogous for those species for which
field data have been collected (L. aurata, L. insularis, L. adolphinae) with larvae infesting decomposing timber, typically subterranean root systems and stumps in the cooler and drier parts of the range in the south and tablelands, and logs and dead standing trees in the more humid portions of the range in the tropics (Reid, et al 2018; Hangay & de Keyzer
2017; Fearn 1996; Suzuki 1995). Species in the genus are strongly
dimorphic with males typically having longer limbs, larger bodies and well developed mandibles in comparison to females (Plate 1). These dimorphic traits are common in lucanids around the world (Goyens et al. 2015). Larger male size and mandibular length appears to be driven by competition for food resources and females (Emlen & Nijhout 2000; Fearn 1996, 2016; Goyens et al. 2015). Males will fight over a prime shoot-tip, and typically the largest male will win and defend it. The adults feed on the sugary liquids that a plant produces when a shoot-tip is cut off. Males use their enlarged mandibles to make this cut, and then the flow of
sap is maintained by the feeding male. It appears to be the scent of the sap that attracts females to the location of the males which facilitates mating (Fearn 1996, 2015, 2016, 2017; Suzuki 1995). Tasmanian L. aurata are the only members of the genus for which adult food plants are well documented. Congregations of both sexes and mating pairs have been collected on the native grass Lomandra longifolia (Fearn 1996), native vine Clematis decipiens (Fearn 2017), coast everlasting Ozothamnus turbinatus (Fearn 2016), drooping she-oak Allocasuarina verticillata (Fearn 2017), gum trees Eucalyptus globulus, E. viminalis and E. ovata (Fearn 1996), ornamental apricot, Prunus armeniaca (Fearn 2015) and red
leaf photinia, Photinia sp. (Fearn 1996). All eucalypt species previously recorded as adult host plants in Tasmania are closely related smooth barked taxa. In this work we document the first record of a feeding aggregation on a 'stringy-barked' eucalypt, the giant ash, Eucalyptus regnans.