This catalogue presents the first-ever complete inventory of all described taxa of Australian weevils, including both valid and invalid names. The geographical scope spans mainland Australia and its continental islands as well as the subantarctic Heard and McDonald Islands, the Pacific Lord Howe and Norfolk Islands and the Indian-Ocean Christmas Island. 4111 species in 832 genera (including one extinct species and one fossil) are recognised as occurring in this territory, distributed over seven families, 20 subfamilies and 94 tribes. The families and subfamilies are arranged in a currently accepted phylogenetic sequence but the tribes, genera and species in alphabetical order. Introductory chapters outline the discovery and composition of the Australian weevil fauna, the burden of synonymy, the format and conventions of the catalogue and the taxonomic and nomenclatural changes proposed. Sixteen new genera and six new species are described, two new names and 25 new generic and 72 new species synonymies and 189 new combinations are proposed and 46 type species designations are effected. The records of 356 taxa are annotated to justify or explain various taxonomic and nomenclatural acts and issues, covering descriptions of new taxa, new synonymies and generic combinations, artificial taxon concepts, changes in classification and a number of nomenclatural matters. The catalogue of the taxa present in Australia is followed by a list of 19 species incorrectly recorded from Australia or introduced as biocontrol agents but not established, and by one species inquirenda. All these records are also annotated. Two appendices list the 102 species introduced into Australia, both accidental and deliberate (as weed control agents). A bibliography with full references of all original descriptions and pertinent other citations from the literature is provided, and an index to all names concludes the catalogue.

Only a few weevils have been described from Burmese amber, and although most have been misclassified, they show unusual and specialised characters unknown in extant weevils. In this paper, we present the results of a study of a much larger and more diverse selection of Burmese amber weevils. We prepared all amber blocks to maximise visibility of structures and examined these with high-magnification light microscopy as well as CT scanning (selected specimens). We redescribe most previously described taxa and describe 52 new species in 26 new genera, accompanied by photographs. We compare critical characters of these weevils with those of extant taxa and outline the effects of distortion on their preservation and interpretation. We conclude that only two weevil families are thus far represented in Burmese amber, Nemonychidae and a newly recognised family, Mesophyletidae, which appears closely related to Attelabidae but cannot be accommodated in this family. The geniculate antennae and long rostrum with exodont mandibles of most Mesophyletidae indicate that they were highly specialised phytophages of early angiosperms preserved in the amber, likely ovipositing in flowers or seeds. This weevil fauna appears to represent an extinct mid-Cretaceous ecosystem and fills a critical gap in the fossil record of weevils.

The first elateroid fossils from the Upper Jurassic Talbragar Fish Bed in Australia are described and illustrated. Wongaroo amplipectorale gen. et sp. n., based on two specimens, is placed in the family Cerophytidae due to its convex, posteriorly weakly angled and laterally carinate pronotum obscuring the head in dorsal view, its relatively long, pointed elytra and slender legs, its 9-striate elytra with deep basal pits and the absence of metacoxal plates. Beattieellus jurassicus gen. et sp. n., described from one specimen, possesses the acutely angled pronotum without a carina on the posterolateral angles and the ventral click apparatus typical of Eucnemidae and is classified in this family. Assignment of it to a eucnemid subfamily is impossible because of the insufficient preservation of relevant characters in the fossil. Four other elateroid fossils, possibly representing eucnemids and elaterids, are illustrated and briefly described but not named, due to their insufficient preservation. These fossils represent the first of their kind in Australia and in the Southern Hemisphere, and Beattieellus is also the oldest eucnemid fossil known and extends the fossil record of Eucnemidae into the Upper Jurassic. The discovery of elateroid fossils in the Talbragar Fish Bed adds to the coleopteran diversity of this ancient lake ecosystem, indicating that it was well wooded and provided suitable habitats of rotten wood for the development of the larvae of these taxa.

The 2016 International Weevil Meeting was held immediately after the International Congress of Entomology (ICE). It built on the topics and content of the 2016 ICE weevil symposium Phylogeny and Evolution of Weevils (Coleoptera: Curculionoidea): A Symposium in Honor of Dr. Guillermo "Willy” Kuschel. Beyond catalyzing research and collaboration, the meeting was intended to serve as a forum for identifying priorities and goals for those who study weevils. The meeting consisted of 46 invited and contributed lectures, discussion sessions and introductory remarks presented by 23 speakers along with eight contributed research posters. These were organized into three convened sessions, each lasting one day: (1) weevil morphology; (2) weevil fossils, biogeography and host/habitat associations; and (3) molecular phylogenetics and classification of weevils. Some of the topics covered included the 1K Weevils Project, major morphological character systems of adult and larval weevils, weevil morphological terminology, prospects for future morphological character discovery, phylogenetic analysis of morphological character data, the current status of weevil molecular phylogenetics and evolution, resources available for phylogenetic and comparative genomic studies of weevils, the weevil fossil record, weevil biogeography and evolution, weevil host plants, evolutionary development of the weevil rostrum, resources available for weevil identification and the current status of and challenges in weevil classification.

Curculionidae are a large mainly herbivorous family of beetles, some of which have become crop pests. Classical biological control has been attempted for about 38 species in 19 genera, and at least moderate success has been achieved in 31 % of cases. Only two weevil species have been considered to be completely controlled by a biological control agent. Success depends upon accurately matching natural enemies with their hosts, and hence taxonomy and phylogeny play a critical role. These factors are discussed and illustrated with two case studies: the introduction of the braconid parasitoid Mictroctonus aethiopoides into New Zealand for biological control of the lucerne pest Sitona discoideus, a case of complex phylogenetic relationships that challenged the prediction of potential non-target hosts, and the use of a mymarid egg parasitoid, Anaphes nitens, to control species of the eucalypt weevil genus Gonipterus, which involves failure to match up parasitoids with the right target amongst a complex of very closely related species. We discuss the increasing importance of molecular methods to support biological control programmes and the essential role of these emerging technologies for improving our understanding of this very large and complex family.

The first Upper Jurassic fossil of the family Ommatidae (Coleoptera: Archostemata) from Australia is described and illustrated from a single specimen discovered at the Talbragar Fish Bed. Rhopalomma stefaniae gen. et sp. n. is classified in Ommatidae based on the length and insertion of the antennae, the tuberculate cuticle, the pattern of elytral striae, the complete epipleura and the presence of scutellary strioles. Due to the lack of preservation of crucial characters, Rhopalomma cannot be assigned to a subfamily and is therefore classified as Ommatidae incertae sedis. Rhopalomma fills an important gap in the fossil record of the family, indicating that Ommatidae occurred in Australia from the Lower Jurassic to the present day. Australia is the only place in the world where this family is found in both the fossil record and the living fauna.