Search

First North American records are presented for Cryptocephalus moraei (Linnaeus, 1758) (Coleoptera: Cryptocephalinae) and Psylliodes dulcamarae (Koch, 1803) (Coleoptera: Galerucinae: Alticini), as confirmed by morphology and DNA barcoding. Additional information is presented about phenology and host use for C. moraei, the first European Cryptocephalinae to be found elsewhere as conclusively adventive. Cryptocephalus moraei is expected to have no ecological impact on its host, the adventive Hypericum perforatum Linnaeus (Hypericaceae). However, P. dulcamarae, the second recently discovered flea beetle associated with the adventive Solanum dulcamara Linnaeus (Solanaceae), probably does harm that host. Both species are hypothesised to have arrived from Europe with woody plant material imported with soil during 1960–1965. A literature review of introduced Chrysomelidae found that Canada and the United States of America are together home to 68–78 species of adventive Chrysomelidae. All non-Bruchinae species among these are both native to Europe and occur either in Canada or both Canada and United States of America, except for intentionally introduced biological control agents and two species that feed on Eucalyptus L’Héritier de Brutelle (Myrtaceae). This suggests a dominant role of accidental introductions of cool-climate European species in recent unplanned additions to the fauna of leaf-feeding Chrysomelidae in North America.

Simple Summary In the era of phylogenomics, new molecular sequencing and computational techniques can aid in resolving phylogenetic relationships that were previously intractable by morphological or limited molecular data. In this study, we used anchored hybrid enrichment—designed to recover DNA sequences from hundreds of single-copy orthologous genes—to resolve the phylogeny of the Elateridae (click-beetles) and establish their placement within superfamily Elateroidea. The resulting data were compatible with published transcriptomes, allowing for integrating our dataset with previously published data. Using a wide range of analyses on these molecular data, we tested hypotheses long-debated in the morphological literature and also the robustness of our phylogenetic inferences. Our results placed the bioluminescent lampyroids (fireflies and relatives) within the click-beetles, challenging the current classification of Elateridae, Lampyridae, Phengodidae, and Rhagophthalmidae. However, despite the large amount of molecular data analyzed, a few nodes with conflicting phylogenetic signals could not be unambiguously resolved. Overall, we recovered well-resolved tree topologies that will serve as a framework for further systematic and evolutionary studies of click-beetles. This work further demonstrates that the click-beetle lineage contains not only pest wireworms, but also many species that benefit agriculture. Abstract Click-beetles (Coleoptera: Elateridae) are an abundant, diverse, and economically important beetle family that includes bioluminescent species. To date, molecular phylogenies have sampled relatively few taxa and genes, incompletely resolving subfamily level relationships. We present a novel probe set for anchored hybrid enrichment of 2260 single-copy orthologous genes in Elateroidea. Using these probes, we undertook the largest phylogenomic study of Elateroidea to date (99 Elateroidea, including 86 Elateridae, plus 5 non-elateroid outgroups). We sequenced specimens from 88 taxa to test the monophyly of families, subfamilies and tribes. Maximum likelihood and coalescent phylogenetic analyses produced well-resolved topologies. Notably, the included non-elaterid bioluminescent families (Lampyridae + Phengodidae + Rhagophthalmidae) form a clade within the otherwise monophyletic Elateridae, and Sinopyrophoridae may not warrant recognition as a family. All analyses recovered the elaterid subfamilies Elaterinae, Agrypninae, Cardiophorinae, Negastriinae, Pityobiinae, and Tetralobinae as monophyletic. Our results were conflicting on whether the hypnoidines are sister to Dendrometrinae or Cardiophorinae + Negastriinae. Moreover, we show that fossils with the eucnemid-type frons and elongate cylindrical shape may belong to Eucnemidae, Elateridae: Thylacosterninae, ancestral hard-bodied cantharoids or related extinct groups. Proposed taxonomic changes include recognition of Plastocerini as a tribe in Dendrometrinae and Hypnoidinae stat. nov. as a subfamily within Elateridae.

The Canadian Entomologist and its associated publications (Supplements of The Canadian Entomologist and Memoirs of the Entomological Society of Canada) have served as important outlets for taxonomic contributions on arthropods since 1868. A survey of beetle (Coleoptera) publications therein has revealed that 2276 species-group, 136 genus-group, and seven family-group taxa were first described in 492 scientific articles. New beetles were described in 67 families by 165 authors. We document trends of beetle descriptions over time, by taxonomic group and by the origin of the new taxa. We also provide biographical notices of the entomologists who described the new taxa. We believe that The Canadian Entomologist will continue to be coveted as a suitable outlet for taxonomic works in the future.

Cardiophorus carinatus Mathison and Douglas sp. nov. (Coleoptera: Elateridae) is described from the Lake Wales Ridge ecosystem of Florida, USA. In addition, C. robustus LeConte, 1853, is rediscovered in North America from Massachusetts, Maine, and Rhode Island.

The prior genus-level classification of Cardiophorinae had never been assessed phylogenetically, and not revised since 1906. A phylogeny for Cardiophorinae and Negastriinae is inferred by Bayesian analyses of 163 adult morphological characters to revise the generic classification. Parsimony analysis is also performed to assess the sensitivity of the Bayesian results to the choice of optimality criterion. Bayesian hypothesis testing rejected monophyly for: Negastriinae; Cardiophorinae (but monophyletic after addition of four taxa); Cardiophorini; cardiophorine genera Aphricus LeConte, 1853; Aptopus Eschscholtz, 1829; Cardiophorus Eschscholtz, 1829; Cardiotarsus Eschscholtz, 1836; Paracardiophorus Schwarz, 1895; Phorocardius Fleutiaux, 1931; Dicronychus sensu Platia, 1994; Dicronychus sensu Méquignon, 1931; Craspedostethus sensu Schwarz, 1906 (i.e., including Tropidiplus Fleutiaux, 1903); Paracardiophorus sensu Cobos, 1970, although well-supported alternative classifications were available for only some. Based on taxonomic interpretation of phylogenetic results: Nyctorini is syn. n. of Cardiophorini; Globothorax Fleutiaux, 1891 (Physodactylinae), Margogastrius Schwarz, 1903 (Physodactylinae), and Pachyelater Lesne, 1897 (Dendrometrinae) are transferred to Cardiophorinae. The following changes are proposed for cardiophorine genera: Aptopus Eschscholtz, 1829 is redefined to exclude Horistonotus-like species; Coptostethus Wollaston, 1854 is subgenus of Cardiophorus; Dicronychus Brullé, 1832 and Diocarphus Fleutiaux, 1947, Metacardiophorus Gurjeva, 1966, Platynychus Motschulsky, 1858, and Zygocardiophorus Iablokoff-Khnzorian and Mardjanian, 1981 are placed at genus rank; Paracardiophorus Schwarz, 1895 is redefined based on North American and Eurasian species only; Horistonotus Candèze, 1860 redefined to include species with multiple apices on each side of their tarsal claws; Patriciella Van Zwaluwenburg, 1953 is syn. n. of Aphricus LeConte, 1853; Teslasena Fleutiaux, 1892 (Physodactylinae) is syn. n. of Globothorax Fleutiaux, 1891. The following new genera are described: Austrocardiophorus (type species: Cardiophorus humeralis Fairmaire and Germain, 1860); Chileaphricus (type species: Aphricus chilensis Fleutiaux, 1940); Floridelater (type species: Coptostethus americanus Horn, 1871, transferred from Negastriinae to Cardiophorinae). Paradicronychus (nomen nudum), is syn. n. of Cardiophorus Eschscholtz, 1829. Generic reassignments to make Cardiodontulus, Cardiophorus, Cardiotarsus, Paracardiophorus consistent with phylogenetically revised genus concepts resulted in 84 new combinations. Lectotypes are designated for 29 type species to fix generic concepts: Anelastes femoralis Lucas, 1857; Aphricus chilensis Fleutiaux, 1940; Athous argentatus Abeille de Perrin, 1894; Cardiophorus adjutor Candèze, 1875; Cardiophorus florentini Fleutiaux, 1895; Cardiophorus inflatus Candèze, 1882; Cardiophorus luridipes Candèze, 1860; Cardiophorus mirabilis Candèze, 1860; Cardiophorus musculus Erichson, 1840; Cardiotarsus capensis Candèze, 1860; Cardiotarsus vitalisi Fleutiaux, 1918; Craspedostethus rufiventris Schwarz, 1898; Elater cinereus Herbst, 1784; Elater minutissimus Germar, 1817; Elater sputator Linnaeus, 1758; Elater thoracicus Fabricius, 1801; Eniconyx pullatus Horn, 1884; Esthesopus castaneus Eschscholtz, 1829; Gastrimargus schneideri Schwarz, 1902; Globothorax chevrolati Fleutiaux, 1891; Horistonotus flavidus Candèze, 1860; Horistonotus simplex LeConte, 1863; Lesnelater madagascariensis Fleutiaux, 1935; Oedostethus femoralis LeConte, 1853; Phorocardius solitarius Fleutiaux, 1931; Platynychus indicus Motschulsky, 1858; Platynychus mixtus Fleutiaux, 1931; Triplonychus acuminatus Candèze, 1860; Tropidiplus tellinii Fleutiaux, 1903. A key to genera and diagnoses are provided for all genera and subgenera. A bibliographic synonymy includes references for all taxonomic changes to genera and new species through 2015.

In this first part of the World catalogue of genus-group names in Elateridae, a nomenclatural review of the genera belonging to ten subfamilies is provided. All names are given with author name, year, and page of publication, type species, and type fixation. We list 132 valid genera in Agrypninae, 2 in Campyloxeninae, 4 in Hemiopinae, 11 in Lissominae, 2 in Oestodinae, 8 in Parablacinae, 2 in Physodactylinae, 2 in Pityobiinae, 1 in Subprotelaterinae, and 7 in Tetralobinae. Genera Anathesis Candèze, 1865, Antitypus Candèze, 1882, Chrostus Candèze, 1878, Dorygonus Candèze, 1859 (with subgenus Rygodonus Fleutiaux, 1932), and Macromalocera Hope, 1834 are tentatively placed as Agrypninae incertae sedis. Paradrapetes villosus Fleutiaux, 1895 is designated as the type species for Paradrapetes Fleutiaux, 1895. Two new gen-era are proposed based on species previously incorrectly used as type species for Abiphis Fleutiaux, 1926 and Lycoreus Candèze, 1857. These genera are Neoabiphis Kundrata & Bouchard, gen. n. (type species: Elater nobilis Illiger, 1800) and Neolycoreus Kundrata & Bouchard, gen. n. (type species: L. regalis Candèze, 1857), respectively. The following new combinations are proposed for species hitherto included in Abiphis Fleutiaux, 1926: Neoabiphis candezei (Alluaud, 1896), comb. n., N. fairmairei (Fleutiaux, 1903), comb. n., N. goudoti (Fleutiaux, 1942), comb. n., N. insignis (Klug, 1833), comb. n., N. nobilis (Illiger, 1800), comb. n., and N. viettei (Girard, 1966), comb. n. The following new combinations are proposed for species hitherto included in Lycoreus Candèze, 1857: Neolycoreus alluaudi (Candèze, 1900), comb. n., N. corpulentus (Candèze, 1899), comb. n., N. cyclops (Candèze, 1865), comb. n., N. decorsei (Fleutiaux, 1903), comb. n., N. dux (Candèze, 1857), comb. n., N. goudotii (Laporte, 1838), comb. n., N. madagascariensis (Gory, 1832), comb. n., N. oculipennis (Fairmaire, 1903), comb. n., N. orbiculatus (Schwarz, 1901), comb. n., N. regalis (Candèze, 1857), comb. n., N. sicardi (Fleutiaux, 1942), comb. n., N. triangularis (Fleutiaux, 1942), comb. n., N. triocellatus (Laporte, 1838), comb. n., and N. vicinus (Fleutiaux, 1942), comb. n. The following new combinations are proposed for species hitherto incorrectly included in Plectrosternus Lacordaire, 1857: Legna rufa (Lacordaire, 1857), comb. n., L. convexa (Vats, 1991), comb. n., L. coolsi (Schimmel, 1996), comb. n., and L. foveata (Patwardhan & Athalye, 2012), comb. n. This research revealed a nomenclatural problem threatening the stability of the well-established valid genus name Adelocera Latreille, 1829. An application to the International Commission on Zoological Nomenclature will be necessary in this case to maintain stability. Additionally, we act here as First Re-visers (ICZN 1999, Art. 24.2) in giving precedence to Lucarius Gistel, 1848 (Staphylinidae) over Lucarius Gistel, 1848 (Elateridae)., This study was supported by the internal grant of the Faculty of Science, UP Olomouc, Czech Republic (IGA_PrF_2019_024; RK, MK), the Moscow State University research project No. АААА-А16-116021660095-7 (AP), and the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Brasil, research grant 304620/2014-9/PQ-Sr (CC).

Elateridae represents one of the largest families within Coleoptera, yet their interrelationships remain under-investigated. Molecular data are missing for most lineages, especially for the species-poor suprageneric taxa. In this study, we investigated the limits and phylogenetic position of Pityobiinae sensu Calder (1996), a group of several small genera from the New World and Australasia, using maximum likelihood and Bayesian inference methods. We merged new sequence data with those deposited in GenBank, producing a final matrix of 178 terminal taxa and covering the main click-beetle subfamilies. The resulting topologies showed Elaterinae as sister to remaining click-beetle lineages, and Agrypninae as sister to the Morostomatinae + Dendrometrinae + Cardiophorinae + Negastriinae clade. Members of Hemiopinae, Lissominae, Thylacosterninae and Pityobiinae formed basal lineages within Elateridae − Elaterinae. We found Lissominae to be polyphyletic, including Thylacosterninae as a terminal lineage and with Oestodini forming an independent lineage outside that clade. Therefore, the subfamily Oestodinae stat. nov. was reinstated for the North American genera Oestodes LeConte and Bladus LeConte. The Australian genera Dicteniophorus Candeze, Drymelater Calder and Stichotomus Candeze were transferred from Dendrometrinae to Elaterinae. Pityobiinae was recovered as two distant lineages in all analyses and correspondingly the subfamily is reduced to contain only the North American Pityobius LeConte and tentatively the South American Tibionema Solier, for which we have no DNA sequences. Additionally, we propose Parablacinae subfam. nov. for the remaining former pityobiine genera from Australia and New Zealand. The new subfamily includes Parablax Schwarz, Metablax Candeze, Wynarka Calder, Xuthelater Calder, Tasmanelater Calder, Parasaphes Candeze and also Ophidius Candeze, which is transferred here from Elaterinae. We failed to find universally diagnostic synapomorphies in adult morphology for Parablacinae, a common problem in elaterid taxonomy. Future research, including a comprehensive phylogeny of the subfamily and re-examination of the morphology of its species is crucial to understanding the limits and classification of this lineage.