Contribution to the weevil fauna (Coleoptera,Curculionoidea) of Turkey

37 species of the weevil families Brentidae, Apionidae, Nanophyidae, Dryophthoridae, Erirhinidae, and Curculionidae are recorded for Turkey or for the Asian part of the country, most of them, for the first time. Some of the species are also newly recorded for other countries.     

A new genus of nemonychid weevil from Burmese amber (Coleoptera,Curculionoidea)

The first fossil nemonychid (Nemonychidae) in Burmese amber, belonging to the subfamily Rhinorhynchinae, is described and figured as Burmonyx zigrasi Davis & Engel, gen. n. and sp. n. While this specimen also comprises the first definitive record of the subfamily in the Asian continent, other compression fossils exist at least from the Yixian Formation of China and the Karatau site of Kazakhstan which may also deserve placement within this group. Although several important areas of the body are obscured by the shape and fragmented condition of the amber piece, a sufficient number of features are visible to consider adequate placement within Rhinorhynchinae, including the fairly strongly punctate elytral striae and appendiculate, nearly bifid pretarsal claws.     

Rostrum structure and development in the rice weevil Sitophilus oryzae (Coleoptera: Curculionoidea: Dryophthoridae)

A documentation and review of weevil rostrum growth is made through examination of the developmental life stages in the rice weevil Sitophilus oryzae (Linnaeus). Histological and morphological examinations are made utilizing light, fluorescent, and electron microscopy. In S. oryzae, rostral tissue begins proliferating in the late 4th instar larva and continues through to the pupal stage, with the majority of rostrum growth taking place in the prepupa. Adult cranial and rostral morphology is also reviewed, focusing on structures that may be pertinent to phylogeny reconstruction. The weevil rostrum is essentially an extension of various head sclerites that are basal to the mouthparts. Therefore, while the mouthparts are fairly similar to other Coleoptera in basic form, the head is markedly different due to its anterior extension. By understanding the more noticeable details of rostrum growth and structure, this study may serve as a foundation for comparative studies of a similar nature and as a basis for beginning research on the genetic nature of rostrum formation and evolution throughout the weevil clade.     

Phylogenetic analysis of the chromate ion transporter (CHR) superfamily

ChrA is a membrane protein that confers resistance to the toxic ion chromate through the energy-dependent chromate efflux from the cytoplasm. In the protein databases, ChrA is a member of the chromate ion transporter (CHR) superfamily, composed of at least several dozens of members, distributed in the three domains of life. The aim of this work was to perform a phylogenetic analysis of the CHR superfamily. An exhaustive search for ChrA homologous proteins was carried out at the National Center for Biotechnology Information database. One hundred and thirty-five sequences were identified as members of the CHR superfamily [77 long-chain sequences, or bidomains (LCHR), and 58 short-chain sequences, or monodomains (SCHR)], organized mainly as tandem pairs of genes whose resultant proteins probably possess oppositely oriented membrane topology. LCHR sequences were split into amino and carboxyl domains, and the resultant domains were aligned with the SCHR proteins. A phylogenetic tree was reconstructed using four different methods, obtaining similar results. The domains were grouped into three clusters: the SCHR proteins cluster, the amino domain cluster of LCHR proteins and the carboxyl domain cluster of LCHR proteins. These results, as well as differences in the genomic context of CHR proteins, enabled the proteins to be sorted into two families (SCHR and LCHR), and 10 subfamilies. Evidence was found suggesting an ancient origin of LCHR proteins from the fusion of two SCHR protein-encoding genes; however, some secondary events of fusion and fission may have occurred later. The separate distribution of the LCHR and SCHR proteins, differences in the genomic context in both groups and the fact that chromate transport has been demonstrated only in LCHR proteins suggest that the CHR proteins comprise two or more paralogous groups in the CHR superfamily.     

Heterochromatic banding patterns on chromosomes of twelve weevil species (Insecta,Coleoptera, Curculionoidea: Apionidae,Curculionidae)

The C-banding patterns of twelve weevil species are presented. The obtained results confirm the existence of two groups of species: with a small or large amount of heterochromatin in the karyotype. The first group comprises seven species (Apionidae: Holotrichapion pisi; Curculionidae: Phyllobius urticae, Ph. pyri, Ph. maculicornis, Tanymecus palliatus, Larinodontes turbinatus, Cionus tuberculosus). In weevils with a small amount of heterochromatin, tiny grains on the nucleus in interphase are visible, afterwards in mitotic and meiotic prophase appearing as dark dots. The absence of C-bands does not indicate a lack of heterochromatin but heterochromatic regions are sometimes so small that the condensation is not visible during the cell cycle. The second group comprises five species (Otiorhynchus niger, O. morio, Polydrusus corruscus, Barypeithes chevrolati, Nedyus quadrimaculatus) which possess much larger heteropicnotic parts of chromosomes visible during all nuclear divisions. The species examined have paracentromeric C-bands on autosomes and the sex chromosome X, except for Otiorhynchus niger, which also has an intercalary bands on one pair of autososomes. All the species examined differ in the size of segments of constitutive heterochromatin. The y heterochromosome is dot-like and wholly euchromatic in all the studied species.     

Phylogenetic analysis of the cadherin superfamily.

Cadherins are a multigene family of proteins which mediate homophilic calcium-dependent cell adhesion and are thought to play an important role in morphogenesis by mediating specific intercellular adhesion. Different lines of experimental evidence have recently indicated that the site responsible for mediating adhesive interactions is localized to the first extracellular domain of cadherin. Based upon an analysis of the sequence of this domain, I show that cadherins can be classified into three groups with distinct structural features. Furthermore, using this sequence information a phylogenetic tree relating the known cadherins was assembled. This is the first such tree to be published for the cadherins. One cadherin subtype, neural cadherin (N-cadherin), shows very little sequence divergence between species, whereas all other cadherin subtypes show more substantial divergence, suggesting that selective pressure upon this domain may be greater for N-cadherin than for other cadherins. Phylogenetic analysis also suggests that the gene duplications which established the main branches leading to the different cadherin subtypes occurred very early in their history. These duplications set the stage for the diversified superfamily we now observe.     

Development of a phylogenetic model for the tribe Micrarctiini (Lepidoptera, Arctiidae) by the SYNAP method

A phylogenetic model for all the 18 genera of Micrarctiini (Lepidoptera, Arctiidae) of the World fauna is discussed. The SYNAP method was used for development of the model. For these purposes, 47 characters of the general appearance, male and female genitalia, and wing pattern were used. Based on these characteristics, an evolutionary trend from the plesiomorphic to apomorphic states was revealed. The genera Apantesis and Amurrhyparia, as well as Notarctia, differ from the other genera to the greatest extent. The other genera have formed two the main clades: Grammia + (Diacrisia + (Rhyparia + Rhyparioides)). Neoarctia + (Palearctia + Holoarctia + Chelis) and all the other genera have occupied separate positions. The latter group was divided into two clades: Ebertarctia + Tancrea + Divarctia with brachypterous females and Centrarctia + (Sibirarctia + (Micrarctia + Hyperborea)).     

Beetles of the superfamily Curculionoidea (Coleoptera) in a complex semi-desert in relation to climate changes in the North Caspian region

In desert and steppe habitats of the complex North Caspian semi-desert, more than twofold differences in the number of hortobiont Curculionoidea species (33 and 75 species, respectively) were observed between the “dry” (1972–1974) and “humid” (2003–2005) climatic phases. The abundance of most species changed. Polyphagous steppe weevils of the subfamily Entiminae (Otiorhynchus velutinus, Euidosomus acuminatus, Omias verruca, and O. rotundatus) with spring activity of adults were the most stable, representing the main dominants of the spring communities both in the 1970s and 2000s. Nearly all of the weevils that changed their abundance since the 1970s were specialized herbivores with summer adult activity. In the more humid 2000s, the abundance of some desert-steppe weevils dominating the desert communities (Phacephorus nebulosus, Metadonus anceps and especially Ptochus porcellus) dropped drastically. Most of the species whose abundance increased most strongly (Phyllobius brevis, Trachyphloeus amplithorax, Archaeophloeus inermis, Stenopterapion tenue, Sitona inops, S. longulus, Tychius spp.) are associated with Medicago romanica, the plant that considerably raised its density in the microdepressions during the “humid” phase. The data show an evident reduction of the most xerophilic (desertsteppe) components of the weevil community and an increase in the fraction of mesophilic species. These changes seem to follow a cyclic pattern.     

Phylogenetic reconstruction of endophytic fungal isolates using internal transcribed spacer 2 (ITS2) region

Endophytic fungi are inhabitants of plants, living most part of their lifecycle asymptomatically which mainly confer protection and ecological advantages to the host plant. In this present study, 48 endophytic fungi were isolated from the leaves of three medicinal plants and characterized based on ITS2 sequence – secondary structure analysis. ITS2 secondary structures were elucidated with minimum free energy method (MFOLD version 3.1) and consensus structure of each genus was generated by 4SALE. ProfDistS was used to generate ITS2 sequence structure based phylogenetic tree respectively. Our elucidated isolates were belonging to Ascomycetes family, representing 5 orders and 6 genera. Colletotrichum/Glomerella spp., Diaporthae/Phomopsis spp., and Alternaria spp., were predominantly observed while Cochliobolus sp., Cladosporium sp., and Emericella sp., were represented by singletons. The constructed phylogenetic tree has well resolved monophyletic groups with >50% bootstrap value support. Secondary structures based fungal systematics improves not only the stability; it also increases the precision of phylogenetic inference. Above ITS2 based phylogenetic analysis was performed for our 48 isolates along with sequences of known ex-types taken from GenBank which confirms the efficiency of the proposed method. Further, we propose it as superlative marker for reconstructing phylogenetic relationships at different taxonomic levels due to their lesser length.     

Phylogenetic reconstruction of the evolution of stylar polymorphisms in Narcissus (Amaryllidaceae)

We investigated the origin of stylar polymorphisms in Narcissus, which possesses a remarkable range of stylar conditions and diverse types of floral morphology and pollination biology. Reconstruction of evolutionary change was complicated by incomplete resolution of trees inferred from two rapidly evolving chloroplast regions, but we bracketed reconstructions expected on the fully resolved plastid-based tree by considering all possible resolutions of polytomies on the shortest trees. Stigma-height dimorphism likely arose on several occasions in Narcissus and persisted across multiple speciation events. As proposed in published models, this rare type of stylar polymorphism is ancestral to distyly. While there is no evidence in Narcissus that dimorphism preceded tristyly, a rapid transition between them may explain the lack of a phylogenetic footprint for this evolutionary sequence. The single instances of distyly and tristyly in Narcissus albimarginatus and N. triandrus, respectively, are clearly not homologous, an evolutionary convergence unique to Amaryllidaceae. Floral morphology was likely an important trigger for the evolution of stylar polymorphisms: Concentrated-changes tests indicate that a long, narrow floral tube may have been associated with the emergence of stigma-height dimorphism and that this type of tube, in combination with a deep corona, likely promoted, or at least was associated with, the parallel origins of heterostyly.     

New Curculionoidea (Coleoptera) records for Canada

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).Published records of Dendroctonus simplex LeConte, 1868 from Northwest Territories should be reassigned to Nunavut, leaving no documented record for NWT. Collection data are provided for eight provincial and national records published without further information previously.     

Construction of the phylogenetic model for the genera of the tribe Arctiini (Lepidoptera,Arctiidae) with the SYNAP method

A new scheme of the phylogeny of the tribe Arctiini is proposed. The Western Mediterranean genus Atlantarctia is considered the most primitive one in the tribe; the rest of genera form two large clades Arctia-Pericallia and Gonerda-Platyprepia. The first clade is supposed to have been subjected to radiation in western Eurasia, and the second clade, in Asia and North America in the Palaeogene when the eastern part of Asia was isolated from western Eurasia. Subsequently, most probably in the Neogene-Pleistocene, representatives of both clades spread over the whole Eurasia and North America. The Arctiini fauna of the tundra zone, which includes the genera Acerbia and Pararctia, was formed in Asia and North America, whereas the subboreal fauna (both steppe and nemoral) originated in western Eurasia. The boreal genus Borearctia has most likely also originated in Asia.     

Phylogenetic reconstruction and shell evolution of the Diplommatinidae (Gastropoda: Caenogastropoda)

The fascinating and often unlikely shell shapes in the terrestrial micromollusc family Diplommatinidae (Gastropoda: Caenogastropoda) provide a particularly attractive set of multiple morphological traits to investigate evolutionary patterns of shape variation. Here, a molecular phylogenetic reconstruction, based on five genes and 2700 bp, was undertaken for this family, integrated with ancestral state reconstruction and phylogenetic PCA of discrete and quantitative traits, respectively. We found strong support for the Diplommatininae as a monophyletic group, separating the Cochlostomatidae into a separate family. Five main clades appear within the Diplommatininae, corresponding with both coiling direction and biogeographic patterns. A Belau clade (A) with highly diverse (but always sinistral) morphology comprised Hungerfordia, Palaina, and some Diplommatina. Arinia (dextral) and Opisthostoma (sinistroid) are sister groups in clade B. Clade C and D solely contain sinistral Diplommatina that are robust and little ornamented (clade C) or slender and sculptured (clade D). Clade E is dextral but biogeographically diverse with species from all sampled regions save the Caroline Islands. Adelopoma, Diplommatina, Palaina, and Hungerfordia require revision to allow taxonomy to reflect phylogeny, whereas Opisthostoma is clearly monophyletic. Ancestral state reconstruction suggests a sinistral origin for the Diplommatinidae, with three reversals to dextrality.     

Phylogenetic diversification of the globin gene superfamily in chordates

Phylogenetic reconstructions provide a means of inferring the branching relationships among members of multigene families that have diversified via successive rounds of gene duplication and divergence. Such reconstructions can illuminate the pathways by which particular expression patterns and protein functions evolved. For example, phylogenetic analyses can reveal cases in which similar expression patterns or functional properties evolved independently in different lineages, either through convergence, parallelism, or evolutionary reversals. The purpose of this article is to provide a robust phylogenetic framework for interpreting experimental data and for generating hypotheses about the functional evolution of globin proteins in chordate animals. To do this, we present a consensus phylogeny of the chordate globin gene superfamily. We document the relative roles of gene duplication and whole-genome duplication in fueling the functional diversification of vertebrate globins, and we unravel patterns of shared ancestry among globin genes from representatives of the three chordate subphyla (Craniata, Urochordata, and Cephalochordata). Our results demonstrate the value of integrating phylogenetic analyses with genomic analyses of conserved synteny to infer the duplicative origins and evolutionary histories of globin genes. We also discuss a number of case studies that illustrate the importance of phylogenetic information when making inferences about the evolution of globin gene expression and protein function. Finally, we discuss why the globin gene superfamily presents special challenges for phylogenetic analysis, and we describe methodological approaches that can be used to meet those challenges.     

Phylogenetic and functional characterization of the hAT transposon superfamily

Transposons are found in virtually all organisms and play fundamental roles in genome evolution. They can also acquire new functions in the host organism and some have been developed as incisive genetic tools for transformation and mutagenesis. The hAT transposon superfamily contains members from the plant and animal kingdoms, some of which are active when introduced into new host organisms. We have identified two new active hAT transposons, AeBuster1, from the mosquito Aedes aegypti and TcBuster from the red flour beetle Tribolium castaneum. Activity of both transposons is illustrated by excision and transposition assays performed in Drosophila melanogaster and Ae. aegypti and by in vitro strand transfer assays. These two active insect transposons are more closely related to the Buster sequences identified in humans than they are to the previously identified active hAT transposons, Ac, Tam3, Tol2, hobo, and Hermes. We therefore reexamined the structural and functional relationships of hAT and hAT-like transposase sequences extracted from genome databases and found that the hAT superfamily is divided into at least two families. This division is supported by a difference in target-site selections generated by active transposons of each family. We name these families the Ac and Buster families after the first identified transposon or transposon-like sequence in each. We find that the recently discovered SPIN transposons of mammals are located within the family of Buster elements.     

Fossil history of Mesozoic weevils (Coleoptera: Curculionoidea)

Abstract The first synopsis of Mesozoic weevils (Curculionoidea: Coleoptera) is presented. Changes of family, genera and species abundance during the Mesozoic revealed three distributional patterns. The Jurassic (Karatau) fauna was dominated by the Nemonychidae. During the Early Cretaceous (beginning at the Jurassic/Cretaceous border), the Ithyceridae was the prevalent group with a significant role played by the Nemonychidae. In the Late Cretaceous (Cenomanian and Turonian), the major groups were the Curculionidae and Brentidae. Obviously, the change of weevil fauna during this period was due to the expansion of the angiosperms, which provided multiple niches in their vegetative and reproductive organs for weevil development.     

Phylogenetic reconstruction of Chirita and allies (Gesneriaceae)with taxonomic treatments

Chirita D. Don, a large genus in the subfamily Cyrtandroideae of Gesneriaceae, has been the subject of much debate whether it is a natural group or not. In addition, the highly heterogeneous Chirita has also been very problematic with regard to delimitation and subdivision. Here we used the nrDNA internal transcribed spacer and cpDNA trnL-F for molecular phylogenetic analaysis, combined with morphological data. Our results suggest that Chirita is an artificial, polyphyletic genus. The most important charact...     

Phylogenetic reconstruction of Polymastiidae (Demospongiae: Hadromerida) based on morphology

Phylogeny of the sponge family Polymastiidae was reconstructed based on 25 morphological characters. Twenty-one polymastiid species and three suberitid species, Suberites domuncula as outgroup, Aaptos aaptos and A. papillata as sister groups, were included in the analyses. The reconstructions were done in PAUP* running heuristic search with the parsimony criterion. We analysed three possible evolutionary scenarios based on three alternative interpretations of the body plan of Quasillina brevis and Ridleia oviformis: first—Ridleia possesses aquiferous papillae whereas Quasillina lacks them, second—both genera lack papillae and third—the body in both genera is a single hyper-developed papilla. All three scenarios excluded the secondary loss of the papillae in the polymastiid evolution. Scenario 2 also excluded the secondary loss of the regular choanosomal skeleton, while scenario 1 assumed its loss in Ridleia and scenario 3 admitted its loss in both Ridleia and Quasillina. We prioritised scenario 2 due to its maximal parsimony and rescaled consistency index and subsequently favoured the clustering of Ridleia and Quasillina separately from the monophyletic polymastiid clade. In all three scenarios Pseudotrachya hystrix clustered separately from other polymastiids in agreement with the molecular evidence, and thus the exclusion of Pseudotrachya from Polymastiidae was proposed. The relationships between A. papillata, Tentorium semisuberites, Polymastia uberrima, the clade Weberella bursa + Polymastia boletiformis and the main polymastiid clade were ambiguous. Meanwhile, all scenarios showed the non-monophyly of Polymastia and Aaptos. Our hypotheses should be tested by reconstructions based on larger taxon sampling of hadromerid species and larger sets of morphological and molecular characters before any ultimate taxonomic decisions are taken.     

New curculionoid beetles (Coleoptera: Curculionoidea) from the Baltic amber

New genera and species of curculionid beetles from the Baltic amber, Pseudoglaesotropis martynovi gen. et sp. nov. (Anthribidae), Palaeometrioxena zherikhini gen. et sp. nov. (Belidae), Eocenorhynchites vossi gen. et sp. nov. (Rhynchitidae), and Archaeosciaphilus marshalli gen. et sp. nov. (Curculionidae), are described.     

The mycetophagidae (coleoptera) of the maritime provinces of Canada

The Mycetophagidae (hairy fungus beetles) of the Maritime Provinces of Canada are surveyed. Seven species in the genera Mycetophagus, Litargus, and Typhaea are found in the region. Six new provincial records are reported including Mycetophagus punctatus and Mycetophagus flexuosus, whichare newly recorded in the Maritime Provinces. The distribution of all species is mapped, colour habitus photographs of all species are figured, and an identification key to species is provided. The discussion notes that four of the species found in the region are apparently rare, possibly due to the history of forest management practices in the region; a situation similar to that of a significant proportion of other saproxylic beetles found in the Maritime Provinces.