A new, but possibly extinct, species of Semanopterus Hope, 1847 from Lord Howe Island, in the southwestern Pacific Ocean (Coleoptera: Scarabaeidae: Dynastinae).

A new and brachypterous species of Semanopterus Hope, 1847 (Coleoptera: Scarabaeidae: Dynastinae: Pentodontini) is described: S. kingstoni Reid & Tees, new species. The species is based on a single female specimen, collected on Lord Howe Island in the southwest Pacific Ocean. It is the sixth species of dynastine known from Lord Howe Island; a key is provided for identification of all of the species known from this small island.

A remarkable new species of the genus Psammoecus Latreille (Coleoptera, Silvanidae) from Lord Howe Island, Australia.

A new species, Psammoecuslordhowensissp. nov., is described from Lord Howe Island, Australia. The new species is brachypterous and most likely endemic to the island. This species is distinct and can be distinguished by the following morphological characters: body rounded and convex; eyes small; temples well developed; lateral pronotal teeth absent; and hind wing strongly reduced.

Taxonomic changes resulting from a review of the types of Australian Anoplognathini (Coleoptera: Scarabaeidae: Rutelinae) housed in Swedish natural history collections.

The type material of Australian Anoplognathini (Coleoptera: Scarabaeidae: Rutelinae) housed in Swedish natural history collections is reviewed, concerning three genera: Anoplognathus Leach, 1815, Amblyterus MacLeay, 1819, and Repsimus MacLeay, 1819. The species were described by G.J. Billberg, J.W. Dalman, L. Gyllenhal, C.J. Schönherr, O. Swartz, and C.P. Thunberg. The contemporary type material of W.S. MacLeay in the Macleay Museum, Sydney, is also examined as it has been overlooked by previous researchers. In total, type specimens for 12 species described between 1817 and 1822 were found in the Naturhistoriska Riksmuseet in Stockholm the Evolutionsmuseet in Uppsala and the Macleay Museum. Five of these species are valid: Anoplognathus brunnipennis, (Gyllenhal, 1817); A. olivieri (Schönherr Dalman, 1817); A. porosus (Dalman, 1817); Amblyterus cicatricosus (Gyllenhal, 1817); and Repsimus manicatus (Swartz, 1817). The other seven species are junior synonyms, as follows (senior synonym first): A. brunnipennis = Rutela chloropyga Thunberg, 1822 (new synonym); A. olivieri = Rutela lacunosa Thunberg, 1822 (new synonym); A. viridiaeneus (Donovan, 1805) = A. latreillei (Schönherr Gyllenhal, 1817); A. viriditarsus Leach, 1815 = Rutela analis Dalman, 1817; and R. manicatus = Anoplognathus brownii W.J. MacLeay, 1819 = A. dytiscoides W. J. MacLeay, 1819 = Rutela ruficollis Thunberg, 1822 (new synonym). Authorship of A. latreillei and A. olivieri is corrected, as noted above. Anoplognathus brunnipennis has been misidentified for the last 60 years at least, leading to the synonymy noted above. Anoplognathus flavipennis Boisduval, 1835 (revised status), is reinstated as the oldest available name for the misidentified A. brunnipennis and the types of A. flavipennis in the Muséum National d'Histoire Naturelle, Paris, are illustrated. Lectotypes are designated for: Anoplognathus brownii, A. flavipennis, A. dytiscoides, Melolontha cicatricosa, Rutela analis, R. brunnipennis, R. lacunosa, R. latreillei, R. manicata, R. olivieri, R. porosa, R. ruficollis, and R. chloropyga. Photographs of all type specimens examined are presented for the first time.

Groehnaltica batophiloides, a new genus and species of flea-beetles (Coleoptera: Chrysomelidae) from Baltic amber, described using X-ray microtomography.

Based on a well-preserved specimen from Eocene Baltic amber, Groehnaltica batophiloides gen. nov. and sp. nov. (Coleoptera: Chrysomelidae: Galerucinae: Alticini) is described and illustrated using X-ray micro-computed tomography (µCT). The new monotypic genus is compared with fossil and extant flea-beetle genera. In the extant Eurasian fauna Groehnaltica shows most similarity to Batophila Foudras, 1859. However, it is also similiar to a Palaeotropical group of genera, including Bikasha Maulik, 1931, and Lanka Maulik, 1926. Groehnaltica batophiloides is the tenth member of Alticini to be described from Baltic amber, adding to our understanding of the evolutionary history of this diverse group of beetles.

Generic Review of New Zealand Chrysomelinae (Coleoptera: Chrysomelidae).

The leaf beetle subfamily Chrysomelinae is reviewed for New Zealand. The native fauna consists of six genera, three new, all of which are described: Aphilon Sharp, 1876; Caccomolpus Sharp, 1886; Chalcolampra Blanchard, 1853; Mauroda gen. nov.; Nanomela gen. nov.; Zeaphilon gen. nov.. Chalcolampra is the senior synonym of Cyrtonogetus Broun, 1915 (comb. nov.). These genera include 51 species, nine newly described and eight in new combinations, as follows: Caccomolpus laticollis (Broun, 1893) comb. nov., from Aphilon; C. pretiosus (Broun, 1880) comb. nov., from Aphilon; Chalcolampra crassa (Broun, 1915) comb. nov., from Cyrtonogetus; Maurodus arcus sp. nov.; M. cinctiger (Broun, 1921) comb. nov., from Caccomolpus; M. impressus (Broun, 1914) comb. nov., from Aphilon; M. lepidus sp. nov.; M. maculatus (Broun, 1893) comb. nov., from Caccomolpus; M. nunni sp. nov.; M. occiduus sp. nov.; M. ornatus (Broun, 1910) comb. nov., from Caccomolpus; M. owenensis sp. nov.; M. plagiatus (Sharp, 1886) comb. nov., from Caccomolpus; M. supernus sp. nov.; Nanomela tiniheke sp. nov.; Zeaphilon marskeae sp. nov.; Z. mirandum sp. nov.. All 11 species in the genus Maurodus are described and a key given for their identification. Type material of the New Zealand species of Aphilon (10 species), Caccomolpus (14 species) and Chalcolampra (13 species) is reviewed and lectotypes designated for 16 species, as well as M. cinctiger. A type species is designated for Caccomolpus: C. globosus Sharp, 1886. Holotypes are confirmed for 26 species. Seven genera and 13 species of exotic Chrysomelinae also occur in New Zealand and their presence is briefly reviewed. One of these exotics has been misnamed as Paropsisterna variicollis (Chapuis, 1877), a junior synonym of P. cloelia (Stål, 1860) (syn. nov.). A key to all genera of Chrysomelinae in New Zealand is provided.

Descriptions of the larva and pupa of Mecynodera balyi Clark, 1864, with notes on its life history (Coleoptera: Chrysomelidae: Sagrinae).

The larva and pupa of the sagrine chrysomelid Mecynodera balyi Clark, 1864 are described and life history notes provided for this species. The larva of Mecynodera balyi is spermophagous and feeds inside seed pods of Pandorea, a vine in the Bignoniaceae. This is the first record of larval spermophagy in any chrysomelid other than Bruchinae, the sister subfamily to Sagrinae. Several morphological features of the immature stages are newly recorded for the Sagrinae. The implications of these new data for systematic placement of Sagrinae are discussed.

Revision of the genus Lamprima Latreille, 1804 (Coleoptera: Lucanidae).

The genus Lamprima Latreille, 1804 (Coleoptera: Lucanidae: Lampriminae: Lamprimini), is revised. Five species are recognised: one in New Guinea (L. adolphinae (Gestro, 1875)), two on isolated western Pacific islands (L. aenea Fabricius, 1792: Norfolk Island; L. insularis W.J. Macleay, 1885: Lord Howe Island), one in northeastern New South Wales (L. imberbis Carter, 1926) and a common widespread species in eastern and southern Australia, L. aurata Latreille, 1817.                   Lamprima aurata varies considerably morphologically and many of the different forms encompassed by this variation have been described as species. Our study of morphology does not support this classification. Therefore, Lamprima aurata is designated a senior synonym of the following 24 names: L. cuprea Latreille, 1817; L. latreillii W.S. MacLeay, 1819 (new synonym); L. pygmaea W.S. MacLeay, 1819 (new synonym); L. fulgida Boisduval, 1835; L. micardi Reiche, 1841 (new synonym); L. rutilans Erichson, 1842; L. splendens Erichson, 1842; L. viridis Erichson, 1842; L. nigricollis Hope in Westwood, 1845 (new synonym); L. purpurascens Hope in Westwood, 1845 (new synonym); L. sumptuosa Hope in Westwood, 1845 (new synonym); L. tasmaniae Hope in Westwood, 1845 (new synonym); L. varians Burmeister, 1847 (new synonym); L. cultridens Burmeister, 1847 (new synonym); L. amplicollis Thomson, 1862 (new synonym); L. krefftii W.J. MacLeay, 1871 (new synonym); L. violacea W.J. Macleay, 1885 (new synonym); L. mandibularis W.J. Macleay, 1885 (new synonym); L. sericea W..J Macleay, 1885 (new synonym); L.nigripennis W.J. Macleay, 1885 (new synonym); L. minima W.J. Macleay, 1885 (new synonym); L. mariae Lea, 1910; L. coerulea Boileau, 1913 (new synonym); L. insularis Boileau, 1913 (new synonym). Lamprima adolphinae is a senior synonym of L. bohni (Darge Séguy, 1953) (new synonym). Lamprima schreibersi Hope in Westwood, 1845, is an unnecessary nomen novum for L. aenea redescribed by Schreibers in 1802 from the same material as Fabricius, and therefore an objective synonym of L. aenea. Lamprima puncticollis Dejean, 1833, L. coerulea Hope in Westwood, 1845, and L. insularis Hope in Westwood, 1845, are nomina nuda, the last two names first made available by Boileau in 1913. The five Lamprima species are redescribed and recommendations made for their conservation. Type specimens of the species of Lamprima described by William Sharpe MacLeay and William John Macleay are illustrated for the first time. Lectotypes are designated for Lamprima insularis, L. latreillii, L. latreillii sericea, and L. mandibularis.

Systemic Vascular Transduction by Capsid Mutant Adeno-Associated Virus After Intravenous Injection.

The ability to effectively deliver genetic material to vascular endothelial cells remains one of the greatest unmet challenges facing the development of gene therapies to prevent diseases with underlying vascular etiology, such as diabetes, atherosclerosis, and age-related macular degeneration. Herein, we assess the effectiveness of an rAAV2-based capsid mutant vector (Y272F, Y444F, Y500F, Y730F, T491V; termed QuadYF+TV) with strong endothelial cell tropism at transducing the vasculature after systemic administration. Intravenous injection of QuadYF+TV resulted in widespread transduction throughout the vasculature of several major organ systems, as assessed by in vivo bioluminescence imaging and postmortem histology. Robust transduction of lung tissue was observed in QuadYF+TV-injected mice, indicating a role for intravenous gene delivery in the treatment of chronic diseases presenting with pulmonary complications, such as α1-antitrypsin deficiency. The QuadYF+TV vector cross-reacted strongly with AAV2 neutralizing antibodies, however, indicating that a targeted delivery strategy may be required to maximize clinical translatability.

Evolution of Spermophagus seed beetles (Coleoptera, Bruchinae, Amblycerini) indicates both synchronous and delayed colonizations of host plants.

Seed beetles are a group of specialized chrysomelid beetles, which are mostly associated with plants of the legume family (Fabaceae). In the legume-feeding species, a marked trend of phylogenetic conservatism of host use has been highlighted by several molecular phylogenetics studies. Yet, little is known about the evolutionary patterns of association of species feeding outside the legume family. Here, we investigate the evolution of host use in Spermophagus, a species-rich seed beetle genus that is specialized on two non-legume host-plant groups: morning glories (Convolvulaceae) and mallows (Malvaceae: Malvoideae). Spermophagus species are widespread in the Old World, especially in the Afrotropical, Indomalaya and Palearctic regions. In this study we rely on eight gene regions to provide the first phylogenetic framework for the genus, along with reconstructions of host use evolution, estimates of divergence times and historical biogeography analyses. Like the legume-feeding species, a marked trend toward conservatism of host use is revealed, with one clade specializing on Convolvulaceae and the other on Malvoideae. Comparisons of plants' and insects' estimates of divergence times yield a contrasted pattern: on one hand a quite congruent temporal framework was recovered for morning-glories and their seed-predators; on the other hand the diversification of Spermophagus species associated with mallows apparently lagged far behind the diversification of their hosts. We hypothesize that this delayed colonization of Malvoideae can be accounted for by the respective biogeographic histories of the two groups.

A new genus and species of Bruchinae, with a key to the genera from Australia (Coleoptera: Chrysomelidae).

A new genus of Bruchinae, Buburra Reid & Beatson, is erected for a single new species, B. jeanae Reid & Beatson. Buburra is endemic to Australia where it is known from a single site at high altitude in Victoria. The hostplant is unknown. Buburra is placed in the tribe Pachymerini. A key is provided for identification of the 12 genera of Bruchinae in Australia, including Caryotrypes Decelle, 1968, recorded from Australia for the first time. Five Australian species described in Bruchus Linneus, 1767, are newly transferred to Bruchidius Schilsky, 1905: Bruchidius diversipes (Lea, 1899) comb. nov.; B. maestus (Lea, 1899) comb. nov.; B. oodnadattae (Blackburn, 1900) comb. nov.; B. persimulans (Blackburn, 1900) comb. nov.; B. quornensis (Blackburn, 1900) comb. nov. A checklist is provided for the species of Bruchinae in Australia.

A new species of Paropsisterna Motschulsky, 1860, a significant pest of plantation eucalypts in Tasmania and Ireland (Coleoptera: Chrysomelidae: Chrysomelinae).

A new species of chrysomeline leaf beetle, Paropsisterna selmani Reid & de Little, is described, including all larval in-stars. This species, native to Australia, is now a significant pest of Eucalyptus plantations in Australia and Ireland, and has been recorded in southern England. Its occurrence in the British Isles represents the first record of establishment of a eucalypt feeding chrysomelid in Europe.

Family-group names in Coleoptera (Insecta).

We synthesize data on all known extant and fossil Coleoptera family-group names for the first time. A catalogue of 4887 family-group names (124 fossil, 4763 extant) based on 4707 distinct genera in Coleoptera is given. A total of 4492 names are available, 183 of which are permanently invalid because they are based on a preoccupied or a suppressed type genus. Names are listed in a classification framework. We recognize as valid 24 superfamilies, 211 families, 541 subfamilies, 1663 tribes and 740 subtribes. For each name, the original spelling, author, year of publication, page number, correct stem and type genus are included. The original spelling and availability of each name were checked from primary literature. A list of necessary changes due to Priority and Homonymy problems, and actions taken, is given. Current usage of names was conserved, whenever possible, to promote stability of the classification.New synonymies (family-group names followed by genus-group names): Agronomina Gistel, 1848 syn. nov. of Amarina Zimmermann, 1832 (Carabidae), Hylepnigalioini Gistel, 1856 syn. nov. of Melandryini Leach, 1815 (Melandryidae), Polycystophoridae Gistel, 1856 syn. nov. of Malachiinae Fleming, 1821 (Melyridae), Sclerasteinae Gistel, 1856 syn. nov. of Ptilininae Shuckard, 1839 (Ptinidae), Phloeonomini Ádám, 2001 syn. nov. of Omaliini MacLeay, 1825 (Staphylinidae), Sepedophilini Ádám, 2001 syn. nov. of Tachyporini MacLeay, 1825 (Staphylinidae), Phibalini Gistel, 1856 syn. nov. of Cteniopodini Solier, 1835 (Tenebrionidae); Agronoma Gistel 1848 (type species Carabus familiaris Duftschmid, 1812, designated herein) syn. nov. of Amara Bonelli, 1810 (Carabidae), Hylepnigalio Gistel, 1856 (type species Chrysomela caraboides Linnaeus, 1760, by monotypy) syn. nov. of Melandrya Fabricius, 1801 (Melandryidae), Polycystophorus Gistel, 1856 (type species Cantharis aeneus Linnaeus, 1758, designated herein) syn. nov. of Malachius Fabricius, 1775 (Melyridae), Sclerastes Gistel, 1856 (type species Ptilinus costatus Gyllenhal, 1827, designated herein) syn. nov. of Ptilinus Geoffroy, 1762 (Ptinidae), Paniscus Gistel, 1848 (type species Scarabaeus fasciatus Linnaeus, 1758, designated herein) syn. nov. of Trichius Fabricius, 1775 (Scarabaeidae), Phibalus Gistel, 1856 (type species Chrysomela pubescens Linnaeus, 1758, by monotypy) syn. nov. of Omophlus Dejean, 1834 (Tenebrionidae). The following new replacement name is proposed: Gompeliina Bouchard, 2011 nom. nov. for Olotelina Báguena Corella, 1948 (Aderidae).Reversal of Precedence (Article 23.9) is used to conserve usage of the following names (family-group names followed by genus-group names): Perigonini Horn, 1881 nom. protectum over Trechicini Bates, 1873 nom. oblitum (Carabidae), Anisodactylina Lacordaire, 1854 nom. protectum over Eurytrichina LeConte, 1848 nom. oblitum (Carabidae), Smicronychini Seidlitz, 1891 nom. protectum over Desmorini LeConte, 1876 nom. oblitum (Curculionidae), Bagoinae Thomson, 1859 nom. protectum over Lyprinae Gistel 1848 nom. oblitum (Curculionidae), Aterpina Lacordaire, 1863 nom. protectum over Heliomenina Gistel, 1848 nom. oblitum (Curculionidae), Naupactini Gistel, 1848 nom. protectum over Iphiini Schönherr, 1823 nom. oblitum (Curculionidae), Cleonini Schönherr, 1826 nom. protectum over Geomorini Schönherr, 1823 nom. oblitum (Curculionidae), Magdalidini Pascoe, 1870 nom. protectum over Scardamyctini Gistel, 1848 nom. oblitum (Curculionidae), Agrypninae/-ini Candèze, 1857 nom. protecta over Adelocerinae/-ini Gistel, 1848 nom. oblita and Pangaurinae/-ini Gistel, 1856 nom. oblita (Elateridae), Prosternini Gistel, 1856 nom. protectum over Diacanthini Gistel, 1848 nom. oblitum (Elateridae), Calopodinae Costa, 1852 nom. protectum over Sparedrinae Gistel, 1848 nom. oblitum (Oedemeridae), Adesmiini Lacordaire, 1859 nom. protectum over Macropodini Agassiz, 1846 nom. oblitum (Tenebrionidae), Bolitophagini Kirby, 1837 nom. protectum over Eledonini Billberg, 1820 nom. oblitum (Tenebrionidae), Throscidae Laporte, 1840 nom. protectum over Stereolidae Rafinesque, 1815 nom. oblitum (Throscidae) and Lophocaterini Crowson, 1964 over Lycoptini Casey, 1890 nom. oblitum (Trogossitidae); Monotoma Herbst, 1799 nom. protectum over Monotoma Panzer, 1792 nom. oblitum (Monotomidae); Pediacus Shuckard, 1839 nom. protectum over Biophloeus Dejean, 1835 nom. oblitum (Cucujidae), Pachypus Dejean, 1821 nom. protectum over Pachypus Billberg, 1820 nom. oblitum (Scarabaeidae), Sparrmannia Laporte, 1840 nom. protectum over Leocaeta Dejean, 1833 nom. oblitum and Cephalotrichia Hope, 1837 nom. oblitum (Scarabaeidae).

DNA barcoding insect-host plant associations.

Short-sequence fragments ('DNA barcodes') used widely for plant identification and inventorying remain to be applied to complex biological problems. Host-herbivore interactions are fundamental to coevolutionary relationships of a large proportion of species on the Earth, but their study is frequently hampered by limited or unreliable host records. Here we demonstrate that DNA barcodes can greatly improve this situation as they (i) provide a secure identification of host plant species and (ii) establish the authenticity of the trophic association. Host plants of leaf beetles (subfamily Chrysomelinae) from Australia were identified using the chloroplast trnL(UAA) intron as barcodes amplified from beetle DNA extracts. Sequence similarity and phylogenetic analyses provided precise identifications of each host species at tribal, generic and specific levels, depending on the available database coverage in various plant lineages. The 76 species of Chrysomelinae included-more than 10 per cent of the known Australian fauna-feed on 13 plant families, with preference for Australian radiations of Myrtaceae (eucalypts) and Fabaceae (acacias). Phylogenetic analysis of beetles shows general conservation of host association but with rare host shifts between distant plant lineages, including a few cases where barcodes supported two phylogenetically distant host plants. The study demonstrates that plant barcoding is already feasible with the current publicly available data. By sequencing plant barcodes directly from DNA extractions made from herbivorous beetles, strong physical evidence for the host association is provided. Thus, molecular identification using short DNA fragments brings together the detection of species and the analysis of their interactions.