Abstract

Biologists have reported on the chemical defences and the phenetic similarity of net-winged beetles (Coleoptera: Lycidae) and their co-mimics. Nevertheless, our knowledge has remained fragmental, and the evolution of mimetic patterns has not been studied in the phylogenetic context. We illustrate the general appearance of ~ 600 lycid species and ~ 200 co-mimics and their distribution. Further, we assemble the phylogeny using the transcriptomic backbone and ~ 570 species. Using phylogenetic information, we closely scrutinise the relationships among aposematically coloured species, the worldwide diversity, and the distribution of aposematic patterns. The emitted visual signals differ in conspicuousness. The uniform coloured dorsum is ancestral and was followed by the evolution of bicoloured forms. The mottled patterns, i.e. fasciate, striate, punctate, and reticulate, originated later in the course of evolution. The highest number of sympatrically occurring patterns was recovered in New Guinea and the Andean mountain ecosystems (the areas of the highest abundance), and in continental South East Asia (an area of moderate abundance but high in phylogenetic diversity). Consequently, a large number of co-existing aposematic patterns in a single region and/or locality is the rule, in contrast with the theoretical prediction, and predators do not face a simple model-like choice but cope with complex mimetic communities. Lycids display an ancestral aposematic signal even though they sympatrically occur with differently coloured unprofitable relatives. We show that the highly conspicuous patterns evolve within communities predominantly formed by less conspicuous Müllerian mimics and, and often only a single species displays a novel pattern. Our work is a forerunner to the detailed research into the aposematic signalling of net-winged beetles.

Highlights

  • Biologists have reported on the chemical defences and the phenetic similarity of net-winged beetles (Coleoptera: Lycidae) and their co-mimics

  • The uniformly black coloured forms are widespread in some regions and supposedly signal their unpalatability by the shape of their body, which provides a strong contrast against translucent leaves and is mimicked by some m­ oths[9,42,43,44] (Fig. 4B,C)

  • This work is a starting point for many future experiments focussing on specific local assemblages, but here we focus in discussing the differences between patterns, as well as their phylogenetic origins, i.e. how old are the principal patterns and whether highly conspicuous patterns rapidly evolved from their cryptic relatives or gradually evolved from the aposematically coloured relatives

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Summary

Introduction

Biologists have reported on the chemical defences and the phenetic similarity of net-winged beetles (Coleoptera: Lycidae) and their co-mimics. Unlike the wellstudied Heliconius system, some lineages of aposematically coloured insects contain up to several hundred species in a single geographic region and up to a hundred species in a single l­ocality[9,10] This means that unpalatable (or more widely unprofitable) aposematically coloured species dynamically interact within complex communities containing multiple patterns, imperfect mimics, as well as Müllerian and Batesian co-mimics. Coloured net-winged beetles can be uniform or display differently coloured body parts, similar to other unprofitable insect p­ rey[13,14,23,41] Further co-mimics are known for the content of toxic or irritating compounds in their bodies and are putative Müllerian mimics (e.g. soldier and blister b­ eetles[17,27,28,52,53,54], Figs. 1I, 4A,C–F)

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