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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 Chinese species of Phorocardius Fleutiaux, 1931 have been studied and six species are described as new: P. alterlineatus Ruan & Douglas, sp. nov.; P. flavistriolatus Ruan & Douglas, sp. nov.; P. minutus Ruan & Douglas, sp. nov.; P. rufiposterus Ruan & Douglas, sp. nov.; P. yunnanensis Ruan & Douglas, sp. nov.; and P. zhiweii Ruan, Douglas & Qiu, sp. nov. Lectotypes are designated for Cardiophorus comptus Candèze, 1860, Cardiophorus contemptus Candèze, 1860, Phorocardius magnus Fleutiaux, 1931, and Cardiophorus manuleatus Candèze, 1888. The holotype is identified for Cardiophorus yanagiharae Miwa, 1927. Phorocardius florentini (Fleutiaux, 1895) and P. manuleatus (Candèze, 1888) are newly reported from China; P. comptus (Candèze, 1860) is excluded from the Chinese fauna. A key to the 11 Phorocardius species known from China is given. Phorocardius is newly recorded from deep within the Palearctic Region. The procoxal cavities of P. rufiposterus Ruan & Douglas, sp. nov. are closed, which is different from all other species of Phorocardius. An annotated checklist of the 21 Phorocardius species of the world is provided. Additionally, Phorocardius contemptus (Candèze, 1860), comb. nov. is transferred from Cardiophorus to Phorocardius; four species are transferred from Phorocardius to Displatynychus: Displatynychus bombycinus (Candèze, 1895), comb. nov., Displatynychus pakistanicus (Platia & Ahmed, 2016), comb. nov., Displatynychus sobrinus (Laporte, 1840), comb. nov., and Displatynychus tibialis (Platia & Ahmed, 2016), comb. nov.

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.

Synopsis of adventive species of Coleoptera (Insecta) recorded from Canada. Part 5: Chrysomeloidea (Cerambycidae, Chrysomelidae, and Megalopodidae)

This study demonstrates the power of DNA barcoding to detect overlooked and newly arrived taxa. Sixty-three species of Coleoptera representing 25 families are studied based on DNA barcode data and morphological analysis of the barcoded specimens. Three of the species involve synonymies or previous taxonomic confusion in North America, while the first Canadian records are published for 60 species. Forty-two species are adventive in North America, and 40 of these adventive species originate from the Palaearctic region. Three genera are recorded from the Nearctic region for the first time:CoelostomaBrullé, 1835 (Hydrophilidae),ScydmoraphesReitter, 1891 (Staphylinidae), andLythrariaBedel, 1897 (Chrysomelidae). Two new synonymies are established:Mycetoporus triangulatusCampbell, 1991 (Staphylinidae) is a junior synonym ofMycetoporus reicheiPandellé, 1869,syn. nov.whileBledius philadelphicusFall, 1919 (Staphylinidae) is a junior synonym ofBledius gallicus(Gravenhorst, 1806),syn. nov.The previously suggested move ofCtenicera tigrina(Fall, 1901) to the genusPseudanostirusDolin, 1964 (Elateridae) is formalized, resulting inPseudanostirus tigrinus(Fall, 1901),comb. nov.

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.

The beetle fauna of Canada was assessed, including estimates of yet unreported diversity using information from taxonomists and COI sequence clusters in a BOLD (Barcode of Life Datasystems) COI dataset comprising over 77,000 Canadian records. To date, 8302 species of Coleoptera have been recorded in Canada, a 23% increase from the first assessment in 1979. A total of 639 non-native beetle species have become established in Canada, with most species in the Staphylinidae (153 spp.), Curculionidae (107 spp.), Chrysomelidae (56 spp.) and Carabidae (55 spp.). Based on estimates from the taxonomic community and our BOLD dataset, we estimate that slightly more than 1000 beetle species remain to be reported from Canada, either as new records or undescribed species. Renewed enthusiasm toward and financial support for surveys, especially in the central and western provinces of Canada will be critical for detecting, documenting and describing these species. The Barcode of Life database is still far from comprehensive for Canadian Coleoptera but substantial progress has been made and the number of Barcode Index Numbers (BINs) (as candidate species) has reached nearly 70% of the number of species reported from Canada. Comparison of BINs to observed species in a group of Canadian Staphylinidae suggests that BINs may provide a good estimate of species diversity within the beetles. Histeridae is a diverse family in Canada that is notably underrepresented in BOLD. Families such as Mordellidae, Scraptiidae, Latridiidae, Ptiliidae and Scirtidae are poorly known taxonomically in Canada and are represented in our BOLD dataset by many more BINs than recorded species.

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).

The formerly monotypic genus Blaiseus, known from Vietnam, is redescribed and nine new species are described and illustrated: B. fujianus new species (P.R. China), B. daklakensis new species (Vietnam), B. laoensis new species (Laos), B. malayensis new species (Malaysia), B. nothoafricanus new species (South Africa), B. zamoranoensis new species (Honduras), B. guatemalensis new species (Guatemala), and B. chiapasensis new species and B. mexicanus new species from Mexico. Morphological character states of the protibia, hind wing and aedeagus not previously observed in Elateridae are described and illustrated. A female specimen of Blaiseus (B. zamoranoensis) is first described here and displays a fossorial morphology type with reduced wings and eyes. Blaiseus is hypothesized to be at least 20 million years old based on its known geographic distribution and apparent female flightlessness.

The following species of Curculionoidea are recorded from Canada for the first time, in ten cases also representing new records at the generic level: Ischnopterapion (Ischnopterapion) loti (Kirby, 1808); Stenopterapion meliloti (Kirby, 1808) (both Brentidae); Atrichonotus taeniatulus (Berg, 1881); Barinus cribricollis (LeConte, 1876); Caulophilus dubius (Horn, 1873); Cionus scrophulariae (Linnaeus, 1758); Cryptorhynchus tristis LeConte, 1876; Cylindrocopturus furnissi Buchanan, 1940; Cylindrocopturus quercus (Say, 1832); Desmoglyptus crenatus (LeConte, 1876); Pnigodes setosus LeConte, 1876; Pseudopentarthrum parvicollis (Casey, 1892); Sibariops confinis (LeConte, 1876); Sibariops confusus (Boheman, 1836); Smicronyx griseus LeConte, 1876; Smicronyx lineolatus Casey, 1892; Euwallacea validus (Eichhoff, 1875); Hylocurus rudis (LeConte, 1876); Lymantor alaskanus Wood, 1978; Phloeotribus scabricollis (Hopkins, 1916); Scolytus oregoni Blackman, 1934; Xyleborus celsus Eichhoff, 1868; Xyleborus ferrugineus (Fabricius, 1801); Xylosandrus crassiusculus (Motschulsky, 1866) (all Curculionidae). In addition the following species were recorded for the first time from these provinces and territories: Yukon – Dendroctonus simplex LeConte, 1868; Phloetribus piceae Swaine, 1911 (both Curculionidae); Northwest Territories – Loborhynchapion cyanitinctum (Fall, 1927) (Brentidae); Nunavut – Dendroctonus simplex LeConte, 1868 (Curculionidae); Alberta – Anthonomus tectus LeConte, 1876; Promecotarsus densus Casey, 1892; Dendroctonus ponderosae Hopkins, 1902; Hylastes macer LeConte, 1868; Rhyncolus knowltoni (Thatcher, 1940); Scolytus schevyrewi Semenov Tjan-Shansky, 1902 (all Curculionidae); Saskatchewan – Phloeotribus liminaris (Harris, 1852); Rhyncolus knowltoni (Thatcher, 1940); Scolytus schevyrewi Semenov Tjan-Shansky, 1902 (all Curculionidae); Manitoba – Cosmobaris scolopacea Germar, 1819; Listronotus maculicollis (Kirby, 1837); Listronotus punctiger LeConte, 1876; Scolytus schevyrewi Semenov Tjan-Shansky, 1902; Tyloderma foveolatum (Say, 1832); (all Curculionidae); Ontario – Trichapion nigrum (Herbst, 1797); Nanophyes marmoratus marmoratus (Goeze, 1777) (both Brentidae); Asperosoma echinatum (Fall, 1917); Micracis suturalis LeConte, 1868; Orchestes alni (Linnaeus, 1758); Phloeosinus pini Swaine, 1915; Scolytus schevyrewi Semenov Tjan-Shansky, 1902; Xyleborinus attenuatus (Blandford, 1894) (all Curculionidae); Quebec – Trigonorhinus alternatus (Say, 1826); Trigonorhinus tomentosus tomentosus (Say, 1826) (both Anthribidae); Trichapion nigrum (Herbst, 1797); Trichapion porcatum (Boheman, 1839); Nanophyes marmoratus marmoratus (Goeze, 1777) (all Brentidae); Lissorhoptrus oryzophilus Kuschel, 1952 (Brachyceridae); Acalles carinatus LeConte, 1876; Ampeloglypter ampelopsis (Riley, 1869); Anthonomus rufipes LeConte, 1876; Anthonomus suturalis LeConte, 1824; Ceutorhynchus hamiltoni Dietz, 1896; Curculio pardalis (Chittenden, 1908); Cyrtepistomus castaneus (Roelofs, 1873); Larinus planus (Fabricius, 1792); Mecinus janthinus (Germar, 1821); Microhyus setiger LeConte, 1876; Microplontus campestris (Gyllenhal, 1837); Orchestes alni (Linnaeus, 1758); Otiorhynchus ligustici (Linnaeus, 1758); Rhinusa neta (Germar, 1821); Trichobaris trinotata (Say, 1832); Tychius liljebladi Blatchley, 1916; Xyleborinus attenuatus (Blandford, 1894); Xyleborus affinis Eichhoff, 1868 (all Curculionidae); Sphenophorus incongruus Chittenden, 1905 (Dryophthoridae); New Brunswick – Euparius paganus Gyllenhal, 1833; Allandrus populi Pierce, 1930; Gonotropis dorsalis (Thunberg, 1796); Euxenus punctatus LeConte, 1876 (all Anthribidae); Loborhynchapion cyanitinctum (Fall, 1927) (Brentidae); Pseudanthonomus seriesetosus Dietz, 1891; Curculio sulcatulus (Casey, 1897); Lignyodes bischoffi (Blatchley, 1916); Lignyodes horridulus (Casey, 1892); Dietzella zimmermanni (Gyllenhal, 1837); Parenthis vestitus Dietz, 1896; Pelenomus squamosus LeConte, 1876; Psomus armatus Dietz, 1891; Rhyncolus macrops Buchanan, 1946; Magdalis inconspicua Horn, 1873; Magdalis salicis Horn, 1873 (all Curculionidae); Nova Scotia – Dryocoetes autographus (Ratzeburg, 1837); Ips perroti Swaine, 1915; Xyleborinus attenuatus (Blandford, 1894) (all Curculionidae); Prince Edward Island – Dryocoetes caryi Hopkins, 1915 (Curculionidae); Newfoundland – Scolytus piceae (Swaine, 1910) (Curculionidae).

The species composition of hoverflies (Syrphidae), click beetles (Elateridae), and bees (Apoidea) was studied to determine whether there was a positive response in these flower-seeking insect groups to gaps in the canopy created through single-tree selection harvesting of Sugar Maple (Acer saccharum) and Yellow Birch (Betula alleghaniensis) in hardwood forests of the Great Lakes-St. Lawrence forest region of Algonquin Provincial Park, Ontario. There were significantly more hoverflies and bees collected in forest stands harvested within the previous five years than in wilderness zone (unharvested at least for 40 years) stands or stands harvested 15-20 years previously (old logged stands). Click beetles, especially Selatosomus pulcher (LeConte), were collected most often in old logged stands. Bees and click beetles were collected significantly later in the season in logged than in wilderness zone stands. Malaise traps resulted in higher capture rates for syrphids than pan traps, and only with these higher capture rates did we detect a significant increase in species richness in recently logged stands over that in wilderness stands. Changes in the numbers and phenology of flower-visiting insects may impact on reproductive success of flowering plants of the forest understory and deserves further study.