Weevil

Because so many species exist in such diversity, the higher classification of weevils is in a state of flux. They are generally divided into two major divisions, the Orthoceri or primitive weevils, and the Gonatoceri or true weevils (Curculionidae). E. C. Zimmerman proposed a third division, the Heteromorphi, for several intermediate forms.[4] Primitive weevils are distinguished by having straight antennae, while true weevils have elbowed (geniculate) antennae. The elbow occurs at the end of the scape (first antennal segment) in true weevils, and the scape is usually much longer than the other antennal segments. Some exceptions occur, such as Nanophyini, primitive weevils with long scapes and geniculate antennae, while among the true weevils, Gonipterinae and Ramphus have short scapes and little or no "elbow".

A 1995 classification system to family level was provided by Kuschel,[5] with updates from Marvaldi et al. in 2002,[6] and was achieved using phylogenetic analyses. The accepted families were the primitive weevils, Anthribidae, Attelabidae, Belidae, Brentidae, Caridae, and Nemonychidae, and the true weevils Curculionidae. Most other weevil families were demoted to subfamilies or tribes. Further work resulted in the elevation of Cimberididae to family from placement as a subfamily of Nemonychidae in 2017[7] and the recognition of the Cretaceous age family Mesophyletidae in 2018 from Burmese amber.[8] The oldest weevils date to the Middle-Late Jurassic boundary, found in the Karabastau Formation of Kazakhstan, the Shar-Teg locality of Mongolia, the Daohugou locality in Inner Mongolia, China, and the Talbragar site in Australia.[9] The extinct family Obrieniidae, with species dating from the Ladinian stage of the Triassic through to tentatively the Oxfordian, have sometimes been considered weevils. Genera of the family have been only found in three formations in Kazakhstan, with most named in 1993.[10] However, their phylogenetic position is contested, with others considering it part of Archostemata.[11]

The interfamilial relationships of Curculionoidea have been generally well resolved.[6][7][12][13][14] The phylogeny by Li et al. (2023) based on phylogenomic data is suggested below:[14]

• Anthribidae—fungus weevils
• Attelabidae—leaf rolling weevils
• Belidae—primitive weevils
• Brentidae—straight snout weevils
• Caridae
• Cimberididae
• Curculionidae—true weevils
• †Mesophyletidae
• Nemonychidae—pine flower weevils
• †?Obrieniidae

Rhopalapion longirostre exhibits an extreme case of sexual dimorphism. The female rostrum is twice as long and its surface is smoother than in the male. The female bores egg channels into the buds of Alcea rosea. Thus, the dimorphism is not attributed to sexual selection. It is a response to ecological demands of egg deposition.[15]

Another example of extreme dimorphism in weevils is that of the New Zealand giraffe weevil, males measure up to 90 mm (3.5 in), and females 50 mm (2.0 in), although there is an extreme range of body sizes in both sexes.

• Bright, Donald E.; Bouchard, Patrice (2008). Coleoptera, Curculionidae, Entiminae: Weevils of Canada and Alaska Volume 2. Insects and Arachnids of Canada Series, Part 25. Ottawa: NRC Research Press. ISBN 978-0-660-19400-4.

• Media related to Curculionoidea at Wikimedia Commons