Abstract.Here we present a phylogeny of beetles (Insecta: Coleoptera) based on DNA sequence data from eight nuclear genes, including six single-copy nuclear protein-coding genes, for 367 species representing 172 of 183 extant families. Our results refine existing knowledge of relationships among major groups of beetles. Strepsiptera was confirmed as sister to Coleoptera and each of the suborders of Coleoptera was recovered as monophyletic. Interrelationships among the suborders, namely Polyphaga (Adephaga (Archostemata, Myxophaga)), in our study differ from previous studies. Adephaga comprised two clades corresponding to Hydradephaga and Geadephaga. The series and superfamilies of Polyphaga were mostly monophyletic. The traditional Cucujoidea were recovered in three distantly related clades. Lymexyloidea was recovered within Tenebrionoidea. Several of the series and superfamilies of Polyphaga received moderate to maximal clade support in most analyses, for example Buprestoidea, Chrysomeloidea, Coccinelloidea, Cucujiformia, Curculionoidea, Dascilloidea, Elateroidea, Histeroidea and Hydrophiloidea. However, many of the relationships within Polyphaga lacked compatible resolution under maximum-likelihood and Bayesian inference, and/or lacked consistently strong nodal support. Overall, we recovered slightly younger estimated divergence times than previous studies for most groups of beetles. The ordinal split between Coleoptera and Strepsiptera was estimated to have occurred in the Early Permian. Crown Coleoptera appeared in the Late Permian, and only one or two lineages survived the end-Permian mass extinction, with stem group representatives of all four suborders appearing by the end of the Triassic. The basal split in Polyphaga was estimated to have occurred in the Triassic, with the stem groups of most series and superfamilies originating during the Triassic or Jurassic. Most extant families of beetles were estimated to have Cretaceous origins. Overall, Coleoptera experienced an increase in diversification rate compared to the rest of Neuropteroidea. Furthermore, 10 family-level clades, all in suborder Polyphaga, were identified as having experienced significant increases in diversification rate. These include most beetle species with phytophagous habits, but also several groups not typically or primarily associated with plants. Most of these groups originated in the Cretaceous, which is also when a majority of the most species-rich beetle families first appeared. An additional 12 clades showed evidence for significant decreases in diversification rate. These clades are species-poor in the Modern fauna, but collectively exhibit diverse trophic habits. The apparent success of beetles, as measured by species numbers, may result from their associations with widespread and diverse substrates -especially plants, but also including fungi, wood and leaf litter -but what facilitated these associations in the first place or has allowed these associations to flourish likely varies within and between lineages. Our results pr...
a b s t r a c tDespite the familiarity and economic significance of Coccinellidae, the family has thus far escaped analysis by rigorous phylogenetic methods. As a result, the internal classification remains unstable and there is no framework with which to interpret evolutionary events within the family. Coccinellids exhibit a wide range of preferred food types spanning kingdoms, and trophic levels. To provide an evolutionary perspective on coccinellid feeding preferences, we performed a phylogenetic analysis of 62 taxa based on the ribosomal nuclear genes 18S and 28S. The entire dataset consists of 3957 aligned nucleotide sites, 787 of which are parsimony informative. Bayesian and parsimony analyses were performed. Host preferences were mapped onto the Bayesian tree to infer food preference transitions. Our results indicate that the ancestral feeding condition for Coccinellidae is coccidophagy. From the ancestral condition, there have been at least three transitions to aphidophagy and one transition to leaf-eating phytophagy. A second transition to leaf-eating phytophagy arose within an aphidophagous/pollinivorous clade. The mycophagous condition in Halyziini originated from aphidophagy. Our findings suggest that polyphagy served as an evolutionary stepping stone for primarily predaceous groups to adopt new feeding habits. The analyses recovered a clade comprising Serangiini plus Microweiseini as the sister group to the rest of Coccinellidae. The subfamilies Coccinellinae and Epilachninae are monophyletic; however, Sticholotidinae, Chilocorinae, Scymninae, and Coccidulinae are paraphyletic. Our results do not support the traditional view of phylogenetic relationships among the coccinellid subfamilies. These results indicate that the current classification system poorly reflects the evolution of Coccinellidae and therefore requires revision.
Abstract.A large-scale phylogenetic study is presented for Cucujoidea (Coleoptera), a diverse superfamily of beetles that historically has been taxonomically difficult. This study is the most comprehensive analysis of cucujoid taxa to date, with DNA sequence data sampled from eight genes (four nuclear, four mitochondrial) for 384 coleopteran taxa, including exemplars of 35 (of 37) families and 289 genera of Cucujoidea. Maximum-likelihood analyses of these data present many significant relationships, some proposed previously and some novel. Tenebrionoidea and Lymexyloidea are recovered together and Cleroidea forms the sister group to this clade. Chrysomeloidea and Curculionoidea are recovered as sister taxa and this clade (Phytophaga) forms the sister group to the core Cucujoidea (Cucujoidea s.n.). The nitidulid series is recovered as the earliest-diverging core cucujoid lineage, although the earliest divergences among core Cucujoidea are only weakly supported. The cerylonid series (CS) is recovered as monophyletic and is supported as a major Cucujiform clade, sister group to the remaining superfamilies of Cucujiformia. Currently recognized taxa that were not recovered as monophyletic include Cucujoidea, Endomychidae, Cerylonidae and Bothrideridae. Biphyllidae and Byturidae were recovered in Cleroidea. The remaining Cucujoidea were recovered in two disparate major clades: one comprising the nitidulid series + erotylid series + Boganiidae and Hobartiidae + cucujid series, and the other comprising the cerylonid series. Propalticidae are recovered within Laemophloeidae. The cerylonid series includes two major clades, the bothriderid group and the coccinellid group. Akalyptoischiidae are recovered as a separate clade from Latridiidae. Eupsilobiinae are recovered as the sister taxon to Coccinellidae. In light of these findings, many formal changes to cucujiform beetle classification are proposed. Biphyllidae and Byturidae are transferred to Cleroidea. The cerylonid series is formally recognized as a new superfamily,
Cladistic analysis of the fire ants of the Solenopsis saevissima species-group (Hymenoptera: Formicidae). 34 ,[493][494][495][496][497][498][499][500][501][502][503][504][505] Results are presented from a phylogenetic study of the fire ants comprising the Solenopsis saevissima species-group (Hymenoptera: Formicidae). Six most-parsimonious trees were identified following a cladistic analysis utilizing 18 taxa and 36 morphological characters derived from three castes and two developmental stages. A strict consensus tree recovered the following relationships: ( S. daguerrei (( S. electra , S. pusilignis ) ( S. saevissima ( S. pythia ( S. interrupta , S. 'undescribed species' , S. weyrauchi ( S. richteri , S. invicta ( S. megergates ( S. quinquecuspis , S. macdonaghi )))))))). This phylogenetic hypothesis implies trends in fire ant evolution towards both polygyny (multiple egg-laying queens per colony) and large major worker size. The phylogeny also provides a test of Emery's Rule, which is not supported in its strictest sense because the social parasite S. daguerrei is not the sister species to its host species. A modified version of Emery's Rule is supported, because the social parasite is the sister species to a larger clade containing its hosts, as well as nonhosts.
We isolated over 650 yeasts over a three year period from the gut of a variety of beetles and characterized them on the basis of LSU rDNA sequences and morphological and metabolic traits. Of these, at least 200 were undescribed taxa, a number equivalent to almost 30% of all currently recognized yeast species. A Bayesian analysis of species discovery rates predicts further sampling of previously sampled habitats could easily produce another 100 species. The sampled habitat is, thereby, estimated to contain well over half as many more species as are currently known worldwide. The beetle gut yeasts occur in 45 independent lineages scattered across the yeast phylogenetic tree, often in clusters. The distribution suggests that the some of the yeasts diversified by a process of horizontal transmission in the habitats and subsequent specialization in association with insect hosts. Evidence of specialization comes from consistent associations over time and broad geographical ranges of certain yeast and beetle species. The discovery of high yeast diversity in a previously unexplored habitat is a first step toward investigating the basis of the interactions and their impact in relation to ecology and evolution.
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