Artykuły w czasopismach na temat „A-186”

The Diptera genus-group names of Camillo Rondani are reviewed and annotated. A total of 601 nomenclaturally available genus-group names in 82 families of Diptera are listed alphabetically. For each name the following are given: author, year and page of original publication, originally included species [and first included species if none were originally included], type species and method of fixation, current status of the name, family placement, and a list of any emendations of it that have been found in the literature. Remarks are given to clarify nomenclatural or taxonomic information. In addition, an index is provided to all the species-group names of Diptera proposed by Rondani (1,236, of which 1,183 are available) with bibliographic reference to each original citation. Appended to this study is a full bibliography of Rondani’s works and a list with explanations for all new synonymies arising from revised emendations. Corrected or clarified type-species and/or corrected or clarified type-species designations are given for the following genus-group names: Anoplomerus Rondani, 1856 [Dolichopodidae]; Biomya Rondani, 1856 [Tachinidae]; Bremia Rondani, 1861 [Cecidomyiidae]; Deximorpha Rondani, 1856 [Tachinidae]; Elasmocera Rondani, 1845 [Asilidae]; Enteromyza Rondani, 1857 [Oestridae]; Exogaster Rondani, 1856 [Tachinidae]; Istocheta Rondani, 1859 [Tachinidae]; Istoglossa Rondani, 1856 [Tachinidae]; Lejogaster Rondani, 1857 [Syrphidae]; Lignodesia Rondani, 1868 [Phaeomyiidae]; Medorilla Rondani, 1856 [Tachinidae]; Meroplius Rondani, 1874 [Sepsidae]; Nodicornis Rondani, 1843 [Dolichopodidae]; Omalostoma Rondani, 1862 [Tachinidae]; Opegiocera Rondani, 1845 [Asilidae]; Petagnia Rondani, 1856 [Tachinidae]; Phaniosoma Rondani, 1856 [Tachinidae]; Proboscina Rondani, 1856 [Tachinidae]; Pyragrura Rondani, 1861 [Tachinidae]; Stemonocera Rondani, 1870 [Tephritidae]; Telejoneura Rondani, 1863 [Asilidae]; Tricoliga Rondani, 1856 [Tachinidae]. The following genus-group names previously treated as available were found to be unavailable: Bombyliosoma Verrall, 1882, n. stat. [Bombyliidae]; Bombylosoma Marschall, 1873, n. stat. [Bombyliidae]; Brachynevra Agassiz, 1846, n. stat. [Cecidomyiidae]; Calliprobola Rondani, 1856, n. stat. [Syrphidae]; Camponeura Verrall, 1882, n. stat. [Syrphidae]; Chlorosoma Verrall, 1882, n. stat. [Stratiomyidae]; Engyzops Verrall, 1882, n. stat. [Calliphoridae]; Exodonta Verrall, 1882, n. stat. [Stratiomyidae]; Histochaeta Verrall, 1882, n. stat. [Tachinidae]; Histoglossa Verrall, 1882, n. stat. [Tachinidae]; Homalostoma Verrall, 1882, n. stat. [Tachinidae]; Hoplacantha Verrall, 1882, n. stat. [Stratiomyidae]; Hoplodonta Verrall, 1882, n. stat. [Stratiomyidae]; Liota Verrall, 1882, n. stat. [Syrphidae]; Lomatacantha Verrall, 1882, n. stat. [Tachinidae]; Machaera Mik, 1890, n. stat. [Tachinidae]; Machaira Brauer & Bergenstamm, 1889, n. stat. [Tachinidae]; Myiatropa Verrall, 1882, n. stat. [Syrphidae]; Oplacantha Verrall, 1882, n. stat. [Stratiomyidae]. Previous First Reviser actions for multiple original spellings missed by previous authors include: Genus-group names—Achanthipodus Rondani, 1856 [Dolichopodidae]; Argyrospila Rondani, 1856 [Bombyliidae]; Botria Rondani, 1856 [Tachinidae]; Chetoliga Rondani, 1856 [Tachinidae]; Chrysoclamys Rondani, 1856 [Syrphidae]; Cyrtophloeba Rondani, 1856 [Tachinidae]; Istocheta Rondani, 1859 [Tachinidae]; Macherea Rondani, 1859 [Tachinidae]; Macronychia Rondani, 1859 [Sarcophagidae]; Pachylomera Rondani, 1856 [Psilidae]; Peratochetus Rondani, 1856 [Clusiidae]; Phytophaga Rondani, 1840 [Cecidomyiidae]; Spylosia Rondani, 1856 [Tachinidae]; Thlipsogaster Rondani, 1863 [Bombyliidae]; Tricogena Rondani, 1856 [Rhinophoridae]; Tricoliga Rondani, 1856 [Tachinidae]; Viviania Rondani, 1861 [Tachinidae]. Species-group name—Sphixapata albifrons Rondani, 1859 [Sarcophagidae]. Acting as First Reviser, the following correct original spellings for multiple original spellings are selected by us: Bellardia Rondani, 1863 [Tabanidae]; Chetoptilia Rondani, 1862 [Tachinidae]; Chetylia Rondani, 1861 [Tachinidae]; Clytiomyia Rondani, 1862 [Tachinidae]; Cryptopalpus Rondani, 1850 [Tachinidae]; Diatomineura Rondani, 1863 [Tabanidae]; Enteromyza Rondani, 1857 [Oestridae]; Esenbeckia Rondani, 1863 [Tabanidae]; Hammomyia Rondani, 1877 [Anthomyiidae]; Hydrothaea Rondani, 1856 [Muscidae]; Hyrmophlaeba Rondani, 1863 [Nemestrinidae]; Limnomya Rondani, 1861 [Limoniidae]; Lyoneura Rondani, 1856 [Psychodidae]; Micetoica Rondani, 1861 [Anisopodidae]; Miennis Rondani, 1869 [Ulidiidae]; Mycetomiza Rondani, 1861 [Mycetophilidae]; Mycosia Rondani, 1861 [Mycetophilidae]; Mycozetaea Rondani, 1861 [Mycetophilidae]; Piotepalpus Rondani, 1856 [Mycetophilidae]; Prothechus Rondani, 1856 [Pipunculidae]; Spyloptera Rondani, 1856 [Limoniidae]; Teremya Rondani, 1875 [Lonchaeidae]; Thricogena Rondani, 1859 [Tachinidae]; Trichopalpus Rondani, 1856 [Scathophagidae]; Trichopeza Rondani, 1856 [Brachystomatidae]; Tricophthicus Rondani, 1861 [Muscidae]; Triphleba Rondani, 1856 [Phoridae]; Xiloteja Rondani, 1863 [Syrphidae]. The following names are new synonymies of their respective senior synonyms: Genus-group names—Acanthipodus Bigot, 1890 of Poecilobothrus Mik, 1878, n. syn. [Dolichopodidae]; Acanthiptera Rondani, 1877 of Achanthiptera Rondani, 1856, n. syn. [Muscidae]; Achantiptera Schiner, 1864 of Achanthiptera Rondani, 1856, n. syn. [Muscidae]; Acydia Rondani, 1870 of Acidia Robineau-Desvoidy, 1830, n. syn. [Tephritidae]; Acyura Rondani, 1863 of Aciura Robineau-Desvoidy, 1830, n. syn. [Tephritidae]; Agaromyia Marschall, 1873 of Agaromya Rondani, 1861, n. syn. [Mycetophilidae]; Ammomyia Mik, 1883 of Leucophora Robineau-Desvoidy, 1830, n. syn. [Anthomyiidae]; Anomoja Rondani, 1871 of Anomoia Walker, 1835, n. syn. [Tephritidae]; Anthracomyia Rondani, 1868 of Morinia Robineau-Desvoidy, 1830, n. syn. [Calliphoridae]; Antracomya Lioy, 1864 of Morinia Robineau-Desvoidy, 1830, n. syn. [Calliphoridae]; Anthoeca Bezzi, 1906 of Solieria Robineau-Desvoidy, 1849, n. syn. [Tachinidae]; Antomyza Rondani, 1866 of Anthomyza Fallén, 1810, n. syn. [Anthomyzidae]; Antracia Rondani, 1862 of Nyctia Robineau-Desvoidy, 1830, n. syn. [Sarcophagidae]; Aporomyia Schiner, 1861 of Lypha Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Asphondilia Rondani, 1861 of Asphondylia Loew, 1850, n. syn. [Cecidomyiidae]; Asteja Rondani, 1856 of Asteia Meigen, 1830, n. syn. [Asteiidae]; Astenia Rondani, 1856 of Blepharicera Macquart, 1843, n. syn. [Blephariceridae]; Astilium Costa, 1866 of Senobasis Macquart, 1838, n. syn. [Asilidae]; Ateleneura Agassiz, 1846 of Atelenevra Macquart, 1834, n. syn. [Pipunculidae]; Athomogaster Rondani, 1866 of Azelia Robineau-Desvoidy, 1830, n. syn. [Muscidae]; Axista Rondani, 1856 of Axysta Haliday, 1839, n. syn. [Ephydridae]; Bigonichaeta Schiner, 1864 of Triarthria Stephens, 1829, n. syn. [Tachinidae]; Billea Rondani, 1862 of Billaea Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Biomyia Schiner, 1868 of Biomya Rondani, 1856, n. syn. [Tachinidae]; Bombilius Dufour, 1833 of Bombylius Linnaeus, 1758, n. syn. [Bombyliidae]; Bombylosoma Loew, 1862 of Bombylisoma Rondani, 1856, n. syn. [Bombyliidae]; Brachipalpus Rondani, 1845 of Brachypalpus Macquart, 1834, n. syn. [Syrphidae]; Brachipalpus Rondani, 1863 of Palpibracus Rondani, 1863, n. syn. [Muscidae]; Brachistoma Rondani, 1856 of Brachystoma Meigen, 1822, n. syn. [Brachystomatidae]; Brachychaeta Brauer & Bergenstamm, 1889 of Brachicheta Rondani, 1861, n. syn. [Tachinidae]; Brachyglossum Bigot, 1858 of Leopoldius Rondani, 1843, n. syn. [Conopidae]; Brachyneura Oken, 1844 of Brachineura Rondani, 1840, n. syn. [Cecidomyiidae]; Caelomya Rondani, 1866 of Fannia Robineau-Desvoidy, 1830, n. syn. [Fanniidae]; Caelomyia Rondani, 1877 of Fannia Robineau-Desvoidy, 1830, n. syn. [Fanniidae]; Caenosia Westwood, 1840 of Coenosia Meigen, 1826, n. syn. [Muscidae]; Campilomiza Rondani, 1840 of Campylomyza Meigen, 1818, n. syn. [Cecidomyiidae]; Campylochaeta Bezzi & Stein, 1907 of Campylocheta Rondani, 1859, n. syn. [Tachinidae]; Caricoea Rondani, 1856 of Coenosia Meigen, 1826, n. syn. [Muscidae]; Carpomyia Loew, 1862 of Carpomya Rondani, 1856, n. syn. [Tephritidae]; Cassidemya Rondani, 1861 of Cassidaemyia Macquart, 1835, n. syn. [Rhinophoridae]; Ceratoxia Costa, 1866 of Otites Latreille, 1804, n. syn. [Ulidiidae]; Ceratoxys Rondani, 1861 of Otites Latreille, 1804, n. syn. [Ulidiidae]; Chaetogena Bezzi & Stein, 1907 of Chetogena Rondani, 1856, n. syn. [Tachinidae]; Chamemyia Rondani, 1875 of Chamaemyia Meigen, 1803, n. syn. [Chamaemyiidae]; Chaetoptilia Bezzi & Stein, 1907 of Chetoptilia Rondani, 1862, n. syn. [Tachinidae]; Chatolyga Bigot, 1892 of Carcelia Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Chersodromya Rondani, 1856 of Chersodromia Haliday, 1851, n. syn. [Hybotidae]; Chetilya Rondani, 1861 of Chetina Rondani, 1856, n. syn. [Tachinidae]; Chilopogon Bezzi, 1902 of Dasypogon Meigen, 1803, n. syn. [Asilidae]; Chiromya Agassiz, 1846 of Chyromya Robineau-Desvoidy, 1830, n. syn. [Chyromyidae]; Chlorisoma Rondani, 1861 of Microchrysa Loew, 1855, n. syn. [Stratiomyidae]; Chorthophila Rondani, 1856 of Phorbia Robineau-Desvoidy, 1830, n. syn. [Anthomyiidae]; Chortofila Rondani, 1843 of Phorbia Robineau-Desvoidy, 1830, n. syn. [Anthomyiidae]; Chriorhyna Rondani, 1845 of Criorhina Meigen, 1822, n. syn. [Syrphidae]; Chrisogaster Rondani, 1868 of Chrysogaster Meigen, 1803, n. syn. [Syrphidae]; Chryorhina Rondani, 1856 of Criorhina Meigen, 1822, n. syn. [Syrphidae]; Chryorhyna Rondani, 1857 of Criorhina Meigen, 1822, n. syn. [Syrphidae]; Chrysoclamys Rondani, 1856 of Ferdinandea Rondani, 1844, n. syn. [Syrphidae]; Chrysomya Rondani, 1856 of Microchrysa Loew, 1855, n. syn. [Stratiomyidae]; Chrysopila Rondani, 1844 of Chrysopilus Macquart, 1826, n. syn. [Rhagionidae]; Chyrosia Rondani, 1866 of Chirosia Rondani, 1856, n. syn. [Anthomyiidae]; Clytiomyia Rondani, 1862 of Clytiomya Rondani, 1861, n. syn. [Tachinidae]; Conopoejus Bigot, 1892 of Conops Linnaeus, 1758, n. syn. [Conopidae]; Criorhyna Rondani, 1865 of Criorhina Meigen, 1822, n. syn. [Syrphidae]; Criptopalpus Rondani, 1863 of Cryptopalpus Rondani, 1850, n. syn. [Tachinidae]; Crysogaster Rondani, 1865 of Chrysogaster Meigen, 1803, n. syn. [Syrphidae]; Crysops Rondani, 1844 of Chrysops Meigen, 1803, n. syn. [Tabanidae]; Cyrthoneura Rondani, 1863 of Graphomya Robineau-Desvoidy, 1830, n. syn. [Muscidae]; Cyrthoplaeba Rondani, 1857 of Cyrtophloeba Rondani, 1856, n. syn. [Tachinidae]; Cyrthosia Rondani, 1863 of Cyrtosia Perris, 1839, n. syn. [Mythicomyiidae]; Cystogaster Walker, 1856 of Cistogaster Latreille, 1829, n. syn. [Tachinidae]; Cyterea Rondani, 1856 of Cytherea Fabricius, 1794, n. syn. [Bombyliidae]; Dactyliscus Bigot, 1857 of Habropogon Loew, 1847, n. syn. [Asilidae]; Dasiphora Rondani, 1856 of Dasyphora Robineau-Desvoidy, 1830, n. syn. [Muscidae]; Dasipogon Dufour, 1833 of Dasypogon Meigen, 1803, n. syn. [Asilidae]; Dasyneura Oken, 1844 of Dasineura Rondani, 1840, n. syn. [Cecidomyiidae]; Dexiomorpha Mik, 1887 of Estheria Robineau-Desvoidy, n. syn. [Tachinidae]; Dichaetophora Becker, 1905 of Dichetophora Rondani, 1868, n. syn. [Sciomyzidae]; Dicheta Rondani, 1856 of Dichaeta Meigen, 1830, n. syn. [Ephydridae]; Dictia Rondani, 1856 of Dictya Meigen, 1803, n. syn. [Sciomyzidae]; Dionea Rondani, 1861 of Dionaea Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Ditricha Rondani, 1871 of Dithryca Rondani, 1856, n. syn. [Tephritidae]; Dolicopeza Rondani, 1856 of Dolichopeza Meigen, 1830, n. syn. [Tipulidae]; Doricera Rondani, 1856 of Dorycera Meigen, 1830, n. syn. [Ulidiidae]; Drimeia Rondani, 1877 of Drymeia Meigen, 1826, n. syn. [Muscidae]; Drimeja Rondani, 1856 of Drymeia Meigen, 1826, n. syn. [Muscidae]; Driomyza Rondani, 1844 of Dryomyza Fallén, 1820, n. syn. [Dryomyzidae]; Driope Rondani, 1868 of Dryope Robineau-Desvoidy, 1830, n. syn. [Dryomyzidae]; Dryomiza Rondani, 1869 of Dryomyza Fallén, 1820, n. syn. [Dryomyzidae]; Dynera Rondani, 1861 of Dinera Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Dytricha Rondani, 1870 of Dithryca Rondani, 1856, n. syn. [Tephritidae]; Elachysoma Rye, 1881 of Elachisoma Rondani, 1880, n. syn. [Sphaeroceridae]; Elaeophila Marschall, 1873 of Eloeophila Rondani, 1856, n. syn. [Limoniidae]; Emerodromya Rondani, 1856 of Hemerodromia Meigen, 1822, n. syn. [Empididae]; Engyzops Bezzi & Stein, 1907 of Eggisops Rondani, 1862, n. syn. [Calliphoridae]; Entomybia Rondani, 1879 of Braula Nitzsch, 1818, n. syn. [Braulidae]; Epidesmya Rondani, 1861 of Acidia Robineau-Desvoidy, 1830, n. syn. [Tephritidae]; Erinnia Rondani, 1856 of Erynnia Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Eristalomyia Kittel & Kreichbaumer, 1872 of Eristalomya Rondani, 1857, n. syn. [Syrphidae]; Esteria Rondani, 1862 of Estheria Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Exatoma Rondani, 1856 of Hexatoma Meigen, 1803, n. syn. [Tabanidae]; Exochila Mik, 1885 of Hammerschmidtia Schummel, 1834, n. syn. [Syrphidae]; Fisceria Rondani, 1856 of Fischeria Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Gedia Rondani, 1856 of Gaedia Meigen, 1838, n. syn. [Tachinidae]; Gimnocheta Rondani, 1859 of Gymnocheta Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Gimnosoma Rondani, 1862 of Gymnosoma Meigen, 1803, n. syn. [Tachinidae]; Gonirhinchus Lioy, 1864 of Myopa Fabricius, 1775, n. syn. [Conopidae]; Gonirhynchus Marschall, 1873 of Myopa Fabricius, 1775, n. syn. [Conopidae]; Gononeura Oldenberg, 1904 of Gonioneura Rondani, 1880, n. syn. [Sphaeroceridae]; Graphomia Rondani, 1862 of Graphomya Robineau-Desvoidy, 1830, n. syn. [Muscidae]; Gymnopha Rondani, 1856 of Mosillus Latreille, 1804, n. syn. [Ephydridae]; Hammobates Rondani, 1857 of Tachytrechus Haliday, 1851, n. syn. [Dolichopodidae]; Harrysia Rondani, 1865 of Lydina Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Hemathobia Rondani, 1862 of Haematobia Le Peletier & Serville, 1828, n. syn. [Muscidae]; Hemerodromya Rondani, 1856 of Hemerodromia Meigen, 1822, n. syn. [Empididae]; Heryngia Rondani, 1857 of Heringia Rondani, 1856, n. syn. [Syrphidae]; Hidropota Lioy, 1864 of Hydrellia Robineau-Desvoidy, 1830, n. syn. [Ephydridae]; Hipostena Rondani, 1861 of Phyllomya Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Hirmophloeba Marschall, 1873 of Hyrmophlaeba Rondani, 1863, n. syn. [Nemestrinidae]; Histricia Rondani, 1863 of Hystricia Macquart, 1843, n. syn. [Tachinidae]; Hoemotobia Rondani, 1856 of Haematobia Le Peletier & Serville, 1828, n. syn. [Muscidae]; Homalomya Rondani, 1866 of Fannia Robineau-Desvoidy, 1830, n. syn. [Fanniidae]; Homalostoma Bezzi & Stein, 1907 of Billaea Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Hoplisa Brauer & Bergenstamm, 1889 of Oplisa Rondani, 1862, n. syn. [Rhinophoridae]; Hydrothaea Rondani, 1856 of Hydrotaea Robineau-Desvoidy, 1830, n. syn. [Muscidae]; Hylara Rondani, 1856 of Hilara Meigen, 1822, n. syn. [Empididae]; Hyrmoneura Rondani, 1863 of Hirmoneura Meigen, 1820, n. syn. [Nemestrinidae]; Ilisomyia Osten Sacken, 1869 of Ormosia Rondani, 1856, n. syn. [Limoniidae]; Istochaeta Marschall, 1873 of Istocheta Rondani, 1859, n. syn. [Tachinidae]; Lamnea Rondani, 1861 of Erioptera Meigen, 1803, n. syn. [Limoniidae]; Lasiophthicus Rondani, 1856 of Scaeva Fabricius, 1805, n. syn. [Syrphidae]; Lestremya Rondani, 1856 of Lestremia Macquart, 1826, n. syn. [Cecidomyiidae]; Lidella De Galdo, 1856 of Lydella Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Lomacantha Lioy, 1864 of Lomachantha Rondani, 1859, n. syn. [Tachinidae]; Lomachanta Schiner, 1864 of Lomachantha Rondani, 1859, n. syn. [Tachinidae]; Loncoptera Rondani, 1856 of Lonchoptera Meigen, 1803, n. syn. [Lonchopteridae]; Lymnophora Blanchard, 1845 of Limnophora Robineau-Desvoidy, 1830, n. syn. [Muscidae]; Macherium Rondani, 1856 of Machaerium Haliday, 1832, n. syn. [Dolichopodidae]; Macrochaetum Bezzi, 1894 of Elachiptera Macquart, 1825, n. syn. [Chloropidae]; Macrochoetum Bezzi, 1892 of Elachiptera Macquart, 1825, n. syn. [Chloropidae]; Macroneura Rondani, 1856 of Diadocidia Ruthe, 1831, n. syn. [Diadocidiidae]; Marshamya Rondani, 1850 of Linnaemya Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Marsilia Bezzi & Stein, 1907 of Tricoliga Rondani, 1859, n. syn. [Tachinidae]; Megachetum Rondani, 1856 of Dasyna Robineau-Desvoidy, 1830, n. syn. [Psilidae]; Megaloglossa Bezzi, 1907 of Platystoma Meigen, 1803, n. syn. [Platystomatidae]; Megera Rondani, 1859 of Senotainia Macquart, 1846, n. syn. [Sarcophagidae]; Melanomyia Rondani, 1868 of Melanomya Rondani, 1856, n. syn. [Calliphoridae]; Melizoneura Bezzi & Stein, 1907 of Melisoneura Rondani, 1861, n. syn. [Tachinidae]; Mesomelaena Bezzi & Stein, 1907 of Mesomelena Rondani, 1859, n. syn. [Sarcophagidae]; Micetina Rondani, 1861 of Mycetophila Meigen, 1803, n. syn. [Mycetophilidae]; Micetobia Rondani, 1861 of Mycetobia Meigen, 1818, n. syn. [Anisopodidae]; Micromyia Oken, 1844 of Micromya Rondani, 1840, n. syn. [Cecidomyiidae]; Miennis Rondani, 1869 of Myennis Robineau-Desvoidy, 1830, n. syn. [Ulidiidae]; Miopina Rondani, 1866 of Myopina Robineau-Desvoidy, 1830, n. syn. [Anthomyiidae]; Morjnia Rondani, 1862 of Morinia Robineau-Desvoidy, 1830, n. syn. [Calliphoridae]; Morphomyia Rondani, 1862 of Stomina Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Myatropa Rondani, 1857 of Myathropa Rondani, 1845, n. syn. [Syrphidae]; Mycetomiza Rondani, 1861 of Mycosia Rondani, 1861, n. syn. [Mycetophilidae]; Myiantha Rondani, 1877 of Fannia Robineau-Desvoidy, 1830, n. syn. [Fanniidae]; Myiathropa Rondani, 1868 of Myathropa Rondani, 1845, n. syn. [Syrphidae]; Myiocera Rondani, 1868 of Dinera Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Myiolepta Rondani, 1868 of Myolepta Newman, 1838, n. syn. [Syrphidae]; Myiospila Rondani, 1868 of Myospila Rondani, 1856, n. syn. [Muscidae]; Myltogramma Rondani, 1868 of Miltogramma Meigen, 1803, n. syn. [Sarcophagidae]; Myntho Rondani, 1845 of Mintho Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Myospyla Rondani, 1862 of Myospila Rondani, 1856, n. syn. [Muscidae]; Napoea Rondani, 1856 of Parydra Stenhammar, 1844, n. syn. [Ephydridae]; Neera Rondani, 1861 of Neaera Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Nemestrina Blanchard, 1845 of Nemestrinus Latreille, 1802, n. syn. [Nemestrinidae]; Nemorea Macquart, 1834 of Nemoraea Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Nevrolyga Agassiz, 1846 of Neurolyga Rondani, 1840, n. syn. [Cecidomyiidae]; Nictia Rondani, 1862 of Nyctia Robineau-Desvoidy, 1830, n. syn. [Sarcophagidae]; Noteromyia Marschall, 1873 of Camilla Haliday, 1838, n. syn. [Camillidae]; Ociptera Rondani, 1862 of Cylindromyia Meigen, 1803, n. syn. [Tachinidae]; Onodonta Rondani, 1866 of Hydrotaea Robineau-Desvoidy, 1830, n. syn. [Muscidae]; Opegiocera Rondani, 1845 of Ancylorhynchus Berthold, 1827, n. syn. [Asilidae]; Ophira Rondani, 1844 of Hydrotaea Robineau-Desvoidy, 1830, n. syn. [Muscidae]; Ornithoeca Kirby, 1880 of Ornithoica Rondani, 1878, n. syn. [Hippoboscidae]; Ornithomyia Macquart, 1835 of Ornithomya Latreille, 1804, n. syn. [Hippoboscidae]; Orthochile Blanchard, 1845 of Ortochile Latreille, 1809, n. syn. [Dolichopodidae]; Oxicera Rondani, 1856 of Oxycera Meigen, 1803, n. syn. [Stratiomyidae]; Oxina Rondani, 1856 of Oxyna Robineau-Desvoidy, 1830, n. syn. [Tephritidae]; Ozyrhinchus Rondani, 1861 of Ozirhincus Rondani, 1840, n. syn. [Cecidomyiidae]; Oxyrhyncus Rondani, 1856 of Ozirhincus Rondani, 1840, n. syn. [Cecidomyiidae]; Pachigaster Rondani, 1856 of Pachygaster Meigen, 1803, n. syn. [Stratiomyidae]; Pachimeria Rondani, 1856 of Pachymeria Stephens, 1829, n. syn. [Empididae]; Pachipalpus Rondani, 1856 of Cordyla Meigen, 1803, n. syn. [Mycetophilidae]; Pachirhyna Rondani, 1845 of Nephrotoma Meigen, 1803, n. syn. [Tipulidae]; Pachirina Rondani, 1840 of Nephrotoma Meigen, 1803, n. syn. [Tipulidae]; Pachistomus Rondani, 1856 of Xylophagus Meigen, 1803, n. syn. [Xylophagidae]; Pangonia Macquart, 1834 of Pangonius Latreille, 1802, n. syn. [Tabanidae]; Pentetria Rondani, 1856 of Penthetria Meigen, 1803, n. syn. [Bibionidae]; Perichaeta Herting, 1984 of Policheta Rondani, 1856, n. syn. [Tachinidae]; Perichoeta Bezzi, 1894 of Policheta Rondani, 1856, n. syn. [Tachinidae]; Phalacromyia Costa, 1866 of Copestylum Macquart, 1846, n. syn. [Syrphidae]; Phicodromia Rondani, 1866 of Malacomyia Westwood, 1840, n. syn. [Coelopidae]; Phillophaga Lioy, 1864 of Asphondylia Loew, 1850, n. syn. [Cecidomyiidae]; Phito Rondani, 1861 of Phyto Robineau-Desvoidy, 1830, n. syn. [Rhinophoridae]; Phitomyptera Lioy, 1864 of Phytomyptera Rondani, 1845, n. syn. [Tachinidae]; Phitophaga Lioy, 1864 of Cecidomyia Meigen, 1803, n. syn. [Cecidomyiidae]; Phloebotomus Rondani, 1856 of Phlebotomus Rondani & Berté, 1840, n. syn. [Psychodidae]; Phorichaeta Brauer & Bergenstamm, 1889 of Periscepsia Gistel, 1848, n. syn. [Tachinidae]; Phrino Rondani, 1861 of Phryno Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Phrixe Rondani, 1862 of Phryxe Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Phthyria Rondani, 1856 of Phthiria Meigen, 1803, n. syn. [Bombyliidae]; Phtyria Rondani, 1863 of Phthiria Meigen, 1803, n. syn. [Bombyliidae]; Phyllodromya Rondani, 1856 of Phyllodromia Zetterstedt, 1837, n. syn. [Empididae]; Phytofaga Rondani, 1843 of Cecidomyia Meigen, 1803, n. syn. [Cecidomyiidae]; Phytomyzoptera Bezzi, 1906 of Phytomyptera Rondani, 1845, n. syn. [Tachinidae]; Platiparea Rondani, 1870 of Platyparea Loew, 1862, n. syn. [Tephritidae]; Platistoma Lioy, 1864 of Platystoma Meigen, 1803, n. syn. [Platystomatidae]; Platychyra Rondani, 1859 of Panzeria Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Platynochetus Rondani, 1845 of Platynochaetus Wiedemann, 1830, n. syn. [Syrphidae]; Polychaeta Schiner, 1868 of Policheta Rondani, 1856, n. syn. [Tachinidae]; Polycheta Schiner, 1861 of Policheta Rondani, 1856, n. syn. [Tachinidae]; Porrhocondyla Agassiz, 1846 of Porricondyla Rondani, 1840, n. syn. [Cecidomyiidae]; Porrycondyla Walker, 1874 of Porricondyla Rondani, 1840, n. syn. [Cecidomyiidae]; Prosopaea Brauer & Bergenstamm, 1889 of Prosopea Rondani, 1861, n. syn. [Tachinidae]; Psicoda Rondani, 1840 of Psychoda Latreille, 1797, n. syn. [Psychodidae]; Psylopus Rondani, 1850 of Sciapus Zeller, 1842, n. syn. [Dolichopodidae]; Pteropectria Rondani, 1869 of Herina Robineau-Desvoidy, 1830, n. syn. [Ulidiidae]; Pterospylus Bigot, 1857 of Syneches Walker, 1852, n. syn. [Hybotidae]; Pticoptera Rondani, 1856 of Ptychoptera Meigen, 1803, n. syn. [Ptychopteridae]; Ptilocheta Rondani, 1857 of Zeuxia Meigen, 1826, n. syn. [Tachinidae]; Ptilochoeta Bezzi, 1894 of Zeuxia Meigen, 1826, n. syn. [Tachinidae]; Ptylocera Rondani, 1861 of Zeuxia Meigen, 1826, n. syn. [Tachinidae]; Ptylops Rondani, 1859 of Macquartia Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Pyragrura Rondani, 1861 of Labigastera Macquart, 1834, n. syn. [Tachinidae]; Pyrrhosia Bezzi & Stein, 1907 of Leskia Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Ragio Scopoli, 1777 of Rhagio Fabricius, 1775, n. syn. [Rhagionidae]; Raimondia Rondani, 1879 of Raymondia Frauenfeld, 1855, n. syn. [Hippoboscidae]; Ramphina Rondani, 1856 of Rhamphina Macquart, 1835, n. syn. [Tachinidae]; Ramphomya Rondani, 1845 of Rhamphomyia Meigen, 1822, n. syn. [Empididae]; Raphium Latreille, 1829 of Rhaphium Meigen, 1803, n. syn. [Dolichopodidae]; Rhynchomyia Macquart, 1835 of Rhyncomya Robineau-Desvoidy, 1830, n. syn. [Rhiniidae]; Rhyncosia Rondani, 1861 of Aphria Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Rhynophora Rondani, 1861 of Rhinophora Robineau-Desvoidy, 1830, n. syn. [Rhinophoridae]; Riphus Rondani, 1845 of Rhyphus Latreille, 1804, n. syn. [Anisopodidae]; Ripidia Rondani, 1856 of Rhipidia Meigen, 1818, n. syn. [Limoniidae]; Sarcopaga Rondani, 1856 of Sarcophaga Meigen, 1826, n. syn. [Sarcophagidae]; Scatomiza Rondani, 1866 of Scathophaga Meigen, 1803, n. syn. [Scathophagidae]; Schaenomyza Rondani, 1866 of Schoenomyza Haliday, 1833, n. syn. [Muscidae]; Sciomiza Rondani, 1856 of Sciomyza Fallén, 1820, n. syn. [Sciomyzidae]; Sciopila Rondani, 1856 of Sciophila Meigen, 1818, n. syn. [Mycetophilidae]; Serromya Rondani, 1856 of Serromyia Meigen, 1818, n. syn. [Ceratopogonidae]; Seseromyia Costa, 1866 of Cosmina Robineau-Desvoidy, 1830, n. syn. [Rhiniidae]; Sibistroma Rondani, 1856 of Sybistroma Meigen, 1824, n. syn. [Dolichopodidae]; Simplecta Rondani, 1856 of Symplecta Meigen, 1830, n. syn. [Limoniidae]; Sinapha Rondani, 1856 of Synapha Meigen, 1818, n. syn. [Mycetophilidae]; Siritta Rondani, 1844 of Syritta Le Peletier & Serville, 1828, n. syn. [Syrphidae]; Somatolia Bezzi & Stein, 1907 of Lydina Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Somomia Rondani, 1862 of Calliphora Robineau-Desvoidy, 1830, n. syn. [Calliphoridae]; Somomyia Rondani, 1868 of Calliphora Robineau-Desvoidy, 1830, n. syn. [Calliphoridae]; Sphixaea Rondani, 1856 of Milesia Latreille, 1804, n. syn. [Syrphidae]; Sphyxaea Rondani, 1856 of Milesia Latreille, 1804, n. syn. [Syrphidae]; Sphyxapata Bigot, 1881 of Senotainia Macquart, 1846, n. syn. [Sarcophagidae]; Sphyximorpha Rondani, 1856 of Sphiximorpha Rondani, 1850, n. syn. [Syrphidae]; Spilomya Rondani, 1857 of Spilomyia Meigen, 1803, n. syn. [Syrphidae]; Spiximorpha Rondani, 1857 of Sphiximorpha Rondani, 1850, n. syn. [Syrphidae]; Spixosoma Rondani, 1857 of Conops Linnaeus, 1758, n. syn. [Conopidae]; Spylographa Rondani, 1871 of Trypeta Meigen, 1803, n. syn. [Tephritidae]; Stenopterix Millet de la Turtaudière, 1849 of Craterina Olfers, 1816, n. syn. [Hippoboscidae]; Stomorhyna Rondani, 1862 of Stomorhina Rondani, 1861, n. syn. [Rhiniidae]; Stomoxis Latreille, 1797 of Stomoxys Geoffroy, 1762, n. syn. [Muscidae]; Syphona Rondani, 1844 of Siphona Meigen, 1803, n. syn. [Tachinidae]; Tachidromya Rondani, 1856 of Tachydromia Meigen, 1803, n. syn. [Hybotidae]; Tachipeza Rondani, 1856 of Tachypeza Meigen, 1830, n. syn. [Hybotidae]; Tanipeza Rondani, 1850 of Tanypeza Fallén, 1820, n. syn. [Tanypezidae]; Teicomyza Rondani, 1856 of Teichomyza Macquart, 1835, n. syn. [Ephydridae]; Telaira Rondani, 1862 of Thelaira Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Teremya Rondani, 1875 of Lonchaea Fallén, 1820, n. syn. [Lonchaeidae]; Thecomya Rondani, 1848 of Thecomyia Perty, 1833, n. syn. [Sciomyzidae]; Thlypsigaster Marschall, 1873 of Amictus Wiedemann, 1817, n. syn. [Bombyliidae]; Thlypsomyza Rondani, 1863 of Amictus Wiedemann, 1817, n. syn. [Bombyliidae]; Thrichogena Bezzi, 1894 of Loewia Egger, 1856, n. syn. [Tachinidae]; Thricogena Rondani, 1859 of Loewia Egger, 1856, n. syn. [Tachinidae]; Thricophticus Rondani, 1866 of Thricops Rondani, 1856, n. syn. [Muscidae]; Thriptocheta Lioy, 1864 of Campichoeta Macquart, 1835, n. syn. [Diastatidae]; Thryptochoeta Bezzi, 1891 of Campichoeta Macquart, 1835, n. syn. [Diastatidae]; Thyreodonta Marschall, 1873 of Stratiomys Geoffroy, 1762, n. syn. [Stratiomyidae]; Toxopora Rondani, 1856 of Toxophora Meigen, 1803, n. syn. [Bombyliidae]; Tricholiga Rondani, 1873 of Tricoliga Rondani, 1856, n. syn. [Tachinidae]; Trichophticus Rondani, 1871 of Thricops Rondani, 1856, n. syn. [Muscidae]; Tricocera Rondani, 1856 of Trichocera Meigen, 1803, n. syn. [Trichoceridae]; Tricolyga Schiner, 1861 of Tricoliga Rondani, 1856, n. syn. [Tachinidae]; Trigliphus Rondani, 1856 of Triglyphus Loew, 1840, n. syn. [Syrphidae]; Tripeta Rondani, 1856 of Trypeta Meigen, 1803, n. syn. [Tephritidae]; Triphera Rondani, 1861 of Tryphera Meigen, 1838, n. syn. [Tachinidae]; Triptocera Lioy, 1864 of Actia Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Tryptocera Macquart, 1844 of Actia Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Uromya Rondani, 1856 of Phania Meigen, 1824, n. syn. [Tachinidae]; Winthemya Rondani, 1859 of Winthemia Robineau-Desvoidy, 1830, n. syn. [Tachinidae]; Xiloteja Rondani, 1863 of Myolepta Newman, 1838, n. syn. [Syrphidae]; Xylomyia Marschall, 1873 of Xylomya Rondani, 1861, n. syn. [Xylomyidae]; Xyloteja Rondani, 1856 of Myolepta Newman, 1838, n. syn. [Syrphidae]; Xyphidicera Rondani, 1845 of Xiphidicera Macquart, 1834, n. syn. [Hybotidae]; Xyphocera Rondani, 1845 of Ancylorhynchus Berthold, 1827, n. syn. [Asilidae]; Zigoneura Rondani, 1840 of Zygoneura Meigen, 1830, n. syn. [Sciaridae]; Zophomya Rondani, 1859 of Zophomyia Macquart, 1835, n. syn. [Tachinidae]. Species-group name—Psalida leucostoma Rondani, 1856 of Ocyptera simplex Fallén, 1815, n. syn. [Tachinidae]. Mycosia Rondani, 1861 is treated here as nomen dubium [Mycetophilidae]; Habropogon heteroneurus Timon-David, 1951 is resurrected from junior synonymy with Asilus striatus Fabricius, 1794, new stat. [Asilidae]. Reversal of precedence is invoked for three cases of subjective synonymy to promote stability in nomenclature: Macquartia monticola Egger, 1856, nomen protectum and Proboscina longipes Rondani, 1856, nomen oblitum [in Tachinidae]; Loewia Egger, 1856, nomen protectum and Thrychogena Rondani, 1856, nomen oblitum [in Tachinidae]; Zygomyia Winnertz, 1863, nomen protectum and Bolithomyza Rondani, 1856, nomen oblitum [in Mycetophilidae].

This catalog lists all 1226 nominal species introduced by Rondani within Diptera (1174 available and 52 unavailable), providing for each available name data on the type locality, type material, current taxonomic status and with remarks on both the collectors and the specialists who have studied this material. The following new synonymies are proposed: Panops aeneus Philippi, 1865 [Acroceridae] under Lasia aenea Rondani, 1863, n. syn.; Panops nigripes Philippi, 1865 [Acroceridae] under Lasia cuprea Rondani, 1863, n. syn.; Tabanus brasiliensis Rondani, 1850 [Tabanidae] under Dichelacera fasciata Walker, 1850, n. syn.; Petagnia subpetiolata Rondani, 1859 [Tachinidae] under Petagnia occlusa Rondani, 1856, n. syn.; Tephritis siderata Rondani, 1868 [Tephritidae] under Hexacinia radiosa (Rondani, 1868), n. syn. Mallophora macquartii Rondani 1851 [Asilidae] is considered as a senior (but invalid) synonym of Mallophora scopipeda Rondani, 1863, n. syn. Paragus mundus Wollaston, 1858 [Syrphidae] is proposed as the valid name for Paragus coadunatus sensu Goeldlin de Tiefenau (1976); Paragus coadunatus Rondani, 1847 [Syrphidae] is reinstated as a junior synonym of Paragus haemorrhous Meigen 1822. Lectotypes are designated herein for the following nominal species: Domomyza anthracipes Rondani, 1875, Domomyza frontella Rondani, 1875 [both in Agromyzidae]; Chorthophila impudica Rondani, 1866 [Anthomyiidae]; Sephanilla sertulata Rondani, 1875 [Aulacigastridae]; Peratochetus lutescens Rondani, 1856 [Clusiidae]; Myopa punctum Rondani, 1857 [Conopidae]; Culex pulcritarsis Rondani, 1872 [Culicidae]; Ephydra ciligena Rondani, 1868 [Ephydridae]; Lonchea scutellaris Rondani, 1875 [Lonchaeidae]; Geomyza pictipennis Rondani, 1875 [Opomyzidae]; Megaglossa vegetationis Rondani, 1869 [Platystomatidae]; Eumerus tuberculatus Rondani, 1857, Merodon varius Rondani, 1845, Paragus mundus Wollaston, 1858, Pipizella neuphritica Rondani, 1868 [all in Syrphidae]; Exorista noctuicida Rondani, 1859, Phoricheta lacrimans Rondani, 1861 [both in Tachinidae]; Tephritis decipiens Rondani, 1871, Tephritis matutina Rondani, 1871, Urophora lejura Rondani, 1870, Urophora venabulata Rondani, 1870, Urophora veruata Rondani, 1870 [all in Tephritidae]. The following nominal species have lectotypes designated according to Article 74.5 of the I.C.Z.N. Code: Chortophila divergens Rondani, 1866, Chortophila incognita Rondani, 1866 [both in Anthomyiidae]; Habropogon doriae Rondani, 1873, Promacus taeniopus Rondani, 1873 [both in Asilidae]; Chelidomyia melbae Rondani, 1879, Myophthiria lygaeoides Rondani, 1878, Ornithomya gestroi Rondani, 1878, Ornithomya hatamensis Rondani, 1878 [all in Hippoboscidae]; Megaglossa corticarum Rondani, 1869 [Platystomatidae]; Elgiva lateritia Rondani, 1868, Tetanocera nigricosta Rondani, 1868, Tetanocera punctifrons Rondani, 1868 [all in Sciomyzidae]; Tabanus justorius Rondani, 1875 [Tabanidae]. The following lectotypes are designated by inference according to Article 74.6 of I.C.Z.N.: Diopsis aethiopica Rondani, 1873, Diopsis latimana Rondani, 1875, Teleopsis breviscopium Rondani, 1875, Teleopsis longiscopium Rondani, 1875 [all in Diopsidae]; Cyclopodia albertisii Rondani, 1878, Myophthiria reduvioides Rondani, 1875 [both in Hippoboscidae]; Myiodella brachialis Rondani, 1873, Senopterina zonalis Rondani, 1875 [all in Platystomatidae]; Stevenia florentina Rondani, 1861 [Rhinophoridae]; Miltogramma punctatella Rondani, 1868 [Sarcophagidae]; Sargus leoninus Rondani, 1875 [Stratiomyidae]; Chrysops alter Rondani, 1875, Chrysops unizonatus Rondani, 1875, Tabanus dives Rondani, 1875, Tabanus fulvissimus Rondani, 1875, Tabanus ignobilis Rondani, 1875 [all in Tabanidae]; Themara hirtipes Rondani, 1875 [Tephritidae]. The following names are new combinations: Diopsis latimana Rondani, 1875 [Diopsidae] is transferred to Teleopsis and kept as a junior synonym of Teleopsis dalmanni (Wiedemann, 1830), comb. nov.; Diopsis lativola Rondani, 1875 [Diopsidae] is transferred to Teleopsis and kept as a junior synonym of Teleopsis dalmanni (Wiedemann, 1830), comb. nov. The following names, previously deemed unavailable, are determined here to be available: Petagnia occlusa Rondani, 1856 [Tachinidae]; Tephritis siderata Rondani, 1868 [Tephritidae]. The following names, previous deemed available, are determined here to be unavailable: Porricondyla albitarsis Rondani, 1840 [Cecidomyiidae], Lucilia cyanicolor Rondani, 1850 [Calliphoridae]; Cephenemya stimulatrix Rondani, 1857 [Oestridae]; Cheilosia nigricornis Rondani, 1844, Cheilosia testacicornis Rondani, 1857, Pelecocera ruficornis Rondani, 1865 [all in Syrphidae]; Cylindrogaster sanguinea Rondani, 1861, Deximorpha cristata Rondani, 1862, Myostoma microcera Rondani, 1856 [all in Tachinidae]; Tripeta exacheta Rondani, 1870 [Tephritidae]. We consider Merodon italicus Rondani 1845 as an unnecessary substitute name for Merodon natans Fabricius, 1794 and confirm it as a junior synonym of Merodon natans Fabricius, 1794. Acting as First Revisers, the following are herein selected as correct original spellings: Trichophthalma philippii Rondani, 1863 [Nemestrinidae]; Sphiximorpha garibaldii Rondani, 1860 [Syrphidae]; Agelanius philippii Rondani, 1863 [Tabanidae]; Exorista achanthina Rondani, 1859, Platychyra brevicauda Rondani, 1865 [Tachinidae]. Species not previously treated in any recent Diptera catalog include the following: Chorthophila limbatella Rondani, 1877, Hylephila melitensis Rondani 1877 [both in Anthomyiidae]; Mya jonicroma Rondani, 1851, Mya versicolor Rondani, 1850, Somomya anulipes Rondani, 1863, Somomyia xanthomera Rondani, 1875 [all in Calliphoridae]; Madiza fabae Rondani, 1876 [Chloropidae]; Psilopus ducalis Rondani, 1850 [Dolichopodidae]; Gymnopa opaca Rondani, 1869 [Ephydridae]; Oedalea bracata Rondani, 1856 [Hybotidae]; Sapromyza albifrons Rondani, 1868, Sapromyza rectinervis Rondani, 1868 [both in Lauxaniidae]; Boletina parmensis Rondani, 1856, Bolithobia lateralis Rondani, 1856, Bolithomyza spinulina Rondani, 1856, Mycetomyza sciarina Rondani, 1856, Pachipalpus calceatus Rondani, 1856 [all in Mycetophilidae]; Lyoneura lugubris Rondani, 1856 [Psychodidae]; Volucella trizonata Rondani, 1875 [Syrphidae]; Echinomya apicalis Rondani, 1848, Echinomya ignobilis Rondani, 1863, Gonia ornata var. repudiata Rondani, 1859, Hyalomyia unicolor Rondani, 1868, Platychyra valida Rondani, 1865, Pyragrura uncinatus Rondani, 1861 [all in Tachinidae]. One species, Bertea subaptera Rondani, 1856, is returned to Diptera from Hymenoptera after examination of the type material.

In 2015, after the discovery of Kepler-186f, the fifth exoplanet in orbit of its star, Kepler-186, we investigated for three new undetected planets in the Kepler-186 system [1]. Of the planets which are owned by the Kepler-186, the first Earth-like planet and far from its star is Kepler-186f. Considering the order of these five discovered planets, there is a strong possibility for the existence of three new and undetected planets. Theoretically, we have recognized these three new planets locating before and after Kepler-186f. The first two new planets, orbit in the gap between Kepler-186e and Kepler-186f, and are called Kepler-186e(X1) and Kepler-186e(X2) respectively. The third planet also orbits in the exterior region of Kepler-186f is called Kepler-186f(X1). Now, after 6 years, we have reinvestigated these findings using the new information and data available.

The relevance of the study lies in the facts that it explores the issues related to the global significance of Dostoevsky’s literary heritage and interdisciplinary approaches to analyzing Russian literature. The significance of the study is stipulated by the current state of scientific knowledge concerning a particular role of literary works in describing and interpreting global political and state processes. The aim of the study is to reconstruct and map Dostoevsky’s geopolitical worldview based on the analysis of his literary and journalistic works. To consider the writer’s works from the standpoint of his involvement into the political issues is the first attempt within Dostoevsky studies. The analysis of Dostoevsky’s literary heritage from a geopolitical perspective was carried out on the basis of Statisticheskiy slovar’ yazyka Dostoevskogo [Statistical Dictionary of Dostoevsky’s Language]. However, since this book does not contain draft notes and earlier versions, preliminary drafts and notebook materials, these texts were intentionally explored. This is the first literary study of its kind which is based on a variety of modern statistical methods. This fact makes it possible to state that the obtained results present new knowledge about Dostoevsky and are of undisputed novelty. The study is focused on big geopolitical subjects, i.e. countries, transnational and national unions, prominent regions; therefore, the present article is only the first stage of the study. In accordance with the conducted analysis and calculations, the following frequency of geopolitical subjects’ mentions is proposed: Russia (4420); France (848); Germany (735); Britain (397); Turkey (304); Siberia (223); Italy (173); Switzerland (172); Poland (145); Austria (141); America (119); Bulgaria (83); Serbia (83); China (49); Spain (40); Montenegro (38); Caucasus (38); Crimea (30); Egypt (26); Greece (23); Hungary (19); Balkans (18); Central Asia (18); Holland (15); Syria (14); Herzegovina (13); Novorossiya (10); Sweden (7); Japan (6); Altai (5); Arabia, Africa, Bosnia, Dagestan, India, Lithuania, Mexico, Sicily, Finland (each 4); Belgium, Iceland, Malta, Peru, Sandwich Islands (each 3); Brazil, Brittany, Denmark, Israel, Moldova, Romania, Sakhalin (each 2); and Galicia (1). The frequency of geopolitical subjects’ mentions by years is as follows: 1877 (2100), 1876 (1516), 1860 (567), 1880 (502), 1872 (388), 1873 (381), 1868 (366), 1862 (328), 1866 (265), 1875 (264), 1869 (170), 1863 (155), 1881 (135), 1867 (128), 1878 (122), 1864 (120), 1859 (102), 1874 (100), 1870 (96), 1856 (75), 1861 (61), 1871 (54), 1865 (52), 1846 (43), 1847 (41), 1849 (38), 1858 (25), 1854 (21), 1848 (15), 1857 (12), 1845 (5), 1843-1844 (3), 1838-1839 (2), 1879 (1); geopolitical subjects were not mentioned in 1841, 1842, 1850, 1851, 1852, 1853, and 1855. he authors express their deep gratitude to M.V. Podrezov for his assistance in preparing this article. Contribution of the authors: the authors contributed equally to this article. The authors declare no conflicts of interests.

Family-group names proposed for beetles belonging to the family Cerambycidae are catalogued and their availability is determined using the rules of the current International Code of Zoological Nomenclature. A synoptic classification of the family summarizes the validity of the names. Type genera of all family-group names are listed and the type species and stems of genera of available family-group names are included. A new family-group name, Elytracanthinini Bousquet (type genus: Elytracanthina Monn, 2005, a replacement name for Elytracantha Lane, 1955) is proposed for Elytracanthinae Lane, 1955. Ichthyosoma armatum Montrouzier, 1855 is designated as type species of Icthyosoma Boisduval, 1835. Reversal of precedence is used to preserve the validity of the following family-group names: Anaglyptides Lacordaire, 1868 (over Anaglyptisidae Gistel, 1848 [Buprestidae]); Dryobiini Arnett, 1962 (over Dryobiadae Gistel, 1856 [Ptinidae]); Hemilophitae Thomson, 1868 (over Amphionychitae Thomson, 1860) and Hétéropsides Lacordaire, 1869 (over Dichophyiaeidae Gistel, 1848). The following family-group names, although junior synonyms, are preserved as valid until an application is submitted to the International Commission on Zoological Nomenclature; in these cases a reversal of precedence could not be applied: Eurypodini Gahan, 1906 (over Zaracinae Pascoe, 1869); Macronides Lacordaire, 1868 (over Enchapteritae Thomson, 1861); Pyresthides Lacordaire, 1868 (over Pseudolepturitae Thomson, 1861 and Erythrinae Pascoe, 1866) and Stenoderinae Pascoe, 1867 (over Syllitae Thomson, 1864). A total of 238 valid cerambycid family-group names (413 available names) are recognized in the following 13 subfamilies: Vesperinae (1 valid family-group name), Oxypeltinae (1), Disteniinae (4), Anoplodermatinae (3), Philinae (1), Parandrinae (2), Prioninae (24), Spondylidinae (5), Necydalinae (1), Lepturinae (8), Lamiinae (80), Dorcasominae (1), and Cerambycinae (107).

Includes the following reviews: pp. 177-180. Tom Lundskær-Nielsen. Ljungs, M. & Ohlander, S., Gleerups engelska grammatik. pp. 180-182. David Isitt. Oakland, J., British Civilization: An Introduction. + MacQueen, D., Americal Social Studies: A University Primer. + Lundén, R. & Srigley, M. (eds.), Ideas and Identities: British and American Culture. pp. 182-183. Jeremy Lane. Watson, G., British Literature since 1945. pp. 183-184. Alistair Davies. Katz, W. & Sternberg Katz, L. (eds.), The Columbia Granger's Guide to Poetry Anthologies. pp. 184-185. Bertil Nolin. Barker, H., Collected Plays, Vol I *Seven Lears; The Pursuit of Good; Golgo: Sermons on pain and privilege *Arguments for a Theatre. pp. 185-186. Alvar Ellegård. MacQueen, D.S., Using Numbers in English. pp. 187-189. Maria Holmgren Troy. Duff, A. & Maley, A., Literature. + McRae, J. & Pantaleoni, L., Chapter & Verse. pp. 189-190. Elleke Boehmer. Grandqvist, R. (ed.), Signs and Signals: Popular Culture in Africa. pp. 190-192. Gunnar Bergh. Bell, A., The Language of News Media. pp. 193-194. Patrick Burke. Jarringron, J.P. (ed.), Modern Irish Drama. p. 194. Göran Kjellmer. Crystal, S. (series editor), Penguin English Linguistics, Vols. 1-5- p. 195. Helena Bergmann. Bradbury, M. & Cooke, J. (eds.), New Writing. pp. 196-198. Birgit Stolt. von Polenz, P., Deutsche Sprachgeschichte vom Spätmittelalter bis zur Gegenwart. Bd. I. Einführung. Grundbegriffe. Deutsch in der frühbürgerlichen Zeit. pp. 198-200. Gustav Korlén. Paul, H., Deutschen Wörterbuch. 9. Aufl. pp. 201-203. Gunnar Magnusson. Linke, A., Nussbaumer, M. & Portmann, P.R., Studienbuch Linguistik. pp. 204-205. Folke Freund. Helbig, G., Deutsche Grammatik. Grundfragen und Abriß. pp. 205-208. Frank-Michael Kirsch. Malchow, H. & Winkels, H. (Hrsg.), Die Zeit danach. Neue deutsche Literatur. pp. 208-210. Christa Grimm. Frisch, C., "Geniestreich". "Lehrstück", "Revolutionsgestammel". Zur Rezeption des Dramas "Marat/Sade" in der Literaturwissenschaft und auf den Bühnen der Bundesrepublik Deutschland, der Deutschen Demokratischen Republik und Schwedens. pp. 210-212. Göran Bornäs. Blinkenberg, A. & Høybye, P., Dansk-fransk ordbog. pp. 212-217. Börje Schlyer. de Troyes, C., Le Chevalier de la Charrette (Lancelot) *Lancelot ou le Chevalier de la Charrette *Le Conte du Graal ou le Roman de Perceval *Lancelot du Lac. pp. 218-220. Ken Benson. Ciplijauskaité, B., La novela femenina contemporánea (1970-1985). Hacia una tipología de la narración en primera persona. pp. 220-222. Kan Benson. Marful Amor, I., Lorca y sus dobles. Interpretación psicoanalítica de la obra dramática y dibujística. p. 223. Redaktionsmeddelande/A Message from the Editors.

We present a review of the Australian species of Rhytiphora Audinet-Serville, 1835, the most speciose longhorn beetle (Cerambycidae) genus in Australia. The morphological definition of the genus is updated, including useful features to distinguish Rhytiphora from closely related genera within Niphonini. Key characteristics of the two molecularly determined subclades are also provided. The collaris group of Rhytiphora is revised and Rhytiphora garnetensis sp. nov. is described from Queensland. A neotype is designated for Saperda collaris Donovan, 1805; lectotypes are designated for R. amicula White, 1859, Symphyletes vestigialis Pascoe, 1864, Symphyletes compos Blackburn, 1902, R. maculosella Blackburn, 1902, R. uniformis Blackburn, 1901, R. piperitia Hope, 1842 and Symphyletes humeralis White, 1858. A number of species complexes that require genetic confirmation before being synonymised (or separated) are discussed. Finally, we provide a new checklist of the Australian Rhytiphora species which, incorporating synonymies and other changes, reduces the total number of species from 206 to 163. The following species have been synonymised (junior synonym listed first): Coptops abdominalis White, 1858 (= Lamia bankii Fabricius, 1775); Penthea adamsae McKeown, 1938 (= Penthea macularia Pascoe, 1867); R. affinis Breuning, 1970 (= Symphyletes farinosus Pascoe, 1863); Prosoplus albidus Aurivillius, 1917 and Prosoplus minimus Breuning, 1938 (= Corrhenes pauxilla Blackburn, 1901); Prosoplus albostriatus Breuning, 1938 and Prosoplus demarzi Breuning, 1963 (= Niphona oblita Pascoe, 1863); Saperda albocincta Guérin-Méneville, 1831, Symphyletes compos Blackburn, 1902, R. donovani Newman, 1851, R. intertincta Pascoe, 1867, R. maculosella Blackburn, 1902, R. parafarinosa Breuning, 1970, R. vermiculosa Breuning, 1970 and Symphyletes vestigialis Pascoe, 1864 (= Saperda collaris); R. albolateraloides Breuning, 1970 (= Platyomopsis cinerascens Aurivillius, 1917); Symphyletes anaglyptus Pascoe, 1867, Saperdopsis armata Thomson, 1864, Symphyletes moratus Pascoe, 1863 and Symphyletes vetustus Pascoe, 1862 (= Lamia pulverulens Boisduval, 1835); Symphyletes arctos Pascoe, 1865 (= Symphyletes fumatus Pascoe, 1864); Pterolophia australica Breuning, 1938 (= Apomecyna nigrita Pascoe, 1859); R. barnardi Breuning, 1982 (= Symphyletes capreolus Pascoe, 1867); Platyomopsis basalis Aurivillius, 1917 (= Saperdopsis ochreobasalis Breuning, 1938); R. corrhenoides Breuning, 1970 (= Corrhenes cruciata Pascoe, 1875); R. dawsoni Breuning, 1970 (= Symphyletes fasciatus Blackburn, 1901); Symphyletes defloratus Pascoe, 1869 (= Symphyletes gallus Pascoe, 1864); Trichoprosoplus demarzi Breuning, 1961 and Paradaxata spinosa Breuning, 1938 (= Paradaxata villosa Breuning, 1938); Prosoplus elongatus Breuning, 1938 (= Prosoplus metallescens Breuning, 1938); Corrhenes flavovittata Breuning, 1938, Saperda funesta Pascoe, 1859, Anaesthetis lepida Germar, 1848 and Cobria rufa Breuning, 1961 (= Saperda paulla Germar, 1848); Corrhenes guttulata Pascoe, 1865, Corrhenes macmillani Gilmour, 1950 and Saperda mystica Pascoe, 1863 (= Saperda stigmatica Pascoe, 1863); Xiphotheopsis hathlioides Breuning, 1961 (= Xiphohathlia lobata Breuning, 1961); Symphyletes iliacus Pascoe, 1866 (= Symphyletes deserti Blackburn, 1896); Saperdopsis laterialba Breuning, 1938 (= Symphyletes satelles Pascoe, 1865); Etaxalus laterialbus Breuning, 1968 (= Achriotypa basalis Pascoe, 1875); Prosoplus laterinigricollis Breuning, 1961 and Prosoplus mediofasciatus Breuning, 1938 (= Niphona bakewelli Pascoe, 1859); R. leucolateralis Breuning, 1970 (= R. subargentata Breuning, 1970); Penthea lichenosa McKeown, 1942 and Penthea obscura Breuning, 1961 (= Penthea scenica Pascoe, 1863); Sysspilotus macleayi Pascoe, 1865 and Menyllus maculicornis Pascoe, 1864 (= Menyllus rotundipennis Breuning, 1968); R. multituberculata Breuning, 1966 (= Saperdopsis sellata Breuning, 1938); Symphyletes nodosus Newman, 1842 (= Acanthocinus piliger Macleay, 1826); Hathliodes pseudomurinus Breuning, 1938 (= Hathliodes virgatus Breuning, 1938); Penthea sectator Pascoe, 1865 (= Penthea crassicollis Pascoe, 1864); R. simsoni Blackburn, 1901 (= R. mista Newman, 1842); Penthea solida Pascoe, 1863 (= Lamia vermicularia Donovan, 1805); Platyomopsis spinosa Thomson, 1864 (= Lamia obliqua Donovan, 1805); R. truncata Breuning, 1940 (= R. piperitia Hope, 1842); R. uniformis Blackburn, 1901 (= Platyomopsis delicatula McKeown, 1948); Mimiphiastus vivesi Breuning, 1978 (= Symphyletes variolosa Pascoe, 1862). Pterolophia bispinosa Breuning, 1938 is renamed to R. subovata new name (junior homonym of Saperdopsis bispinosa Breuning, 1938), R. browni McKeown, 1938 is reinstated as its own species, and Corrhenes flavovittata demarzi Breuning, 1963 is elevated to species status and renamed R. rentzi new name (junior homonym of Trichoprosoplus demarzi).

The beetle superfamily Curculionoidea includes 43 species associated with Araucaria angustifolia trees in South Brazil. These weevil species belong to the families Nemonychidae (Brarus Kuschel, 1997, Rhynchitoplesius Voss, 1952), Brentidae (Taphroderes Schönherr, 1826) and Curculionidae, the latter including the subfamilies Curculioninae (Heilipodus Kuschel, 1955, Spermologus Schönherr, 1843), Cossoninae (Araucarius Kuschel, 1966, Eurycorynophorus Voss, 1964), Scolytinae (Ambrosiodmus Hopkins, 1915, Araptus Eichhoff, 1871, Cnesinus LeConte, 1868, Corthylus Erichson, 1836, Cryptocarenus Eggers, 1936, Hypothenemus Westwood, 1834, Monarthrum Kirsch, 1866, Pagiocerus Eichhoff, 1868, Phloeotribus Latreille, 1896, Pityophthorus Eichhoff, 1864, Xylechinosomus Schedl, 1963, Xyleborus Eichhoff, 1864, Xyleborinus Reitter, 1913) and Platypodinae (Cenocephalus Chapuis, 1865, Platypus Herbst, 1893, Tesserocerus Saunders, 1836). A checklist of all species including remarks on their life histories and taxonomic notes are presented. In addition, a key for the identification of adult Curculionoidea associated with Araucaria angustifolia to genus or species level is provided.

Search for low-spin signature inversion in the πi13/2 ⊗ νi13/2 bands in odd-odd 182,184,186 Au has been conducted through the standard in-beam γ-spectroscopy techniques. The experiments for 182 Au and 186 Au have been performed in the Japan Atomic Energy Agency (JAEA) via the 152 Sm (35 Cl ,5 n )182 Au and 172 Yb (19 F ,5 n )186 Au reactions, respectively. A study of 184 Au has been made using a multi-detector array GASP in LNL, Italy, via the 159 Tb (29 Si ,4 n )184 Au reaction. The πi13/2 ⊗ νi13/2 bands in these three nuclei have been identified and extended up to high-spin states. In particular, the inter-band connection between the πi13/2 ⊗ νi13/2 band and the ground-state band in 184 Au has been established, leading to a firm spin-and-parity assignment for the πi13/2 ⊗ νi13/2 band. The low-spin signature inversion is found in the πi13/2 ⊗ νi13/2 bands in 182,184,186 Au according to our spin-assignment and the signature crossing observed at high-spin states.

O artigo investiga a aplicação prática dos preceitos constitucionais relativos à função social da propriedade rural e à desapropriação por interesse social para fins de reforma agrária nas decisões do Tribunal Regional Federal da Terceira Região, no interregno entre 2003 e 2011. Com isto em vista, analisaremos os diferentes posicionamentos oriundos da interpretação dos artigos 184, 185, II e 186 da Constituição Federal, para, posteriormente, explorarmos a tendência interpretativa do Tribunal objeto de estudo, especialmente quanto ao conteúdo atribuído à expressão “propriedade produtiva”.

Aims. The differences between the 2007 and the 2013 ASCO/CAP HER2 guidelines have been compared. We also discussed the potential consequences in our pathological practice. Material and Methodology. 189 HER2 fluorescence in situ hybridisation (FISH) tests were performed from 1016 preliminary HER2 immunohistochemical tests (IHC). All cases were reviewed and reclassed following the 2007 and 2013 ASCO/CAP recommendations. Results. The 2013 version decreased false-negative IHC (3/118 versus 1/54, P=ns) and created more 2+ IHC (40/186 versus 89/186, P=0.001) or more 3+ IHC (9/186 versus 39/186, P=0.001). One false-positive IHC was described for the 2013 version (0/9 versus 1/39, P=ns). Equivocal FISH was reduced (8/186 versus 2/186, P=ns). An estimation based on our data for 1000 patients showed a rise of our FISH tests for the control of 2+ IHC (180 tests for the 2007 version versus 274 tests for the 2013 version or FISH work overflow is +52%) and for the control of 2+/3+ IHC (300 for the 2007 version versus 475 for the 2013 version or FISH work overflow is +58%). Conclusions. The new 2013 ASCO/CAP guidelines have detected more HER2 positive cases but have increased the number of FISH tests.

Rhenium-186 (Re-186) has attracted attention as a medical isotope. The feasibility of producing Re-185, the raw material for Re-186, using a fast reactor was evaluated using a continuous energy Monte Carlo code. The irradiation of natural tantalum (Ta) in the fast reactor can produce Re-185 with an isotopic purity of 99%. A two-step irradiation process with different moderators was found to improve the production rate of Re-185. Specifically, this can be achieved by using zirconium hydride (ZrH1.7) as a moderator in the first transmutation process from natural Ta to tungsten (W), and then zirconium deuteride (ZrD1.7) as a moderator in the second transmutation process from W to Re-185. Due to the two-step irradiation, the production rate of Re-185 from Ta can be increased up to a maximum of 470 times compared with irradiation without a moderator, and 2.3 g of Re-185 can be obtained from 1571 g of Ta in 1 year of irradiation. The proposed isotope production method is a new method that is different from the conventional electromagnetic enrichment process.

The content of this article concerns the controversial issue regarding the scope of application of Articles 185 and 186 of the Penal and Fiscal Code (PFC) regulating the substitute forms of enforcing the unpaid fine imposed for criminal fiscal acts. The author attempts to resolve whether the above-mentioned provisions of PFC shall be applied both to the cases of a default on payment and failure to enforce a fine imposed for fiscal offences and fiscal transgressions or only to fines imposed for fiscal transgressions. The paper concludes that Articles 45 and 46 of PFC in conjunction with Article 178 § 1 of PFC, and not specific provisions of Articles 185 and 186 of PFC, shall apply to unenforced fines imposed against perpetrators of fiscal offences. In order to eliminate basic interpretation discrepancies, which may lead to jurisdiction disparity and consequently to unequal treatment of perpetrators sentenced to a fine for criminal fiscal acts of a varied weight, the regulatory intervention may seem required here.

Ever since the publication of Henry Thoreau's four posthumous essay collections, bibliographers and biographers have credited Ralph Waldo Emerson, in the case of Excursions (1863), or William Ellery Channing, in the case of The Maine Woods (1864), Cape Cod (1865), and A Yankee in Canada (1866), with either editing the collections or co-editing them with Sophia Thoreau, Henry's younger sister. This essay provides evidence from letters, books, diaries, and articles, as well as from the essay manuscripts themselves, that Sophia Thoreau alone edited her brother's essay collections for publication after his death from tuberculosis in 1862. She alone also chose the editor for her brother's Journal before her death in 1876.

AbstractAll species-group names of Trachypachidae, Rhysodidae, and Carabidae (including cicindelincs) correctly recorded from America north of Mexico are catalogued with state and province records. Valid names are listed with the author(s), date of publication, and page citation in their current and original combinations while all synonyms are provided in their original combinations. Genus-group names are recorded with the author(s), date of publication, page citation, type species, and kind of type species fixation. Species groups were preferred to subgenera but subscneric names are also listed.The following nomenclatural changes are proposed and discussed: Bembidion neocoerulescens Bousquet, new replacement name for B. coerulescens Van Dyke, 1925; Chlaenius circumcinctus Say, 1830 for C. perplexus Dejean, 1831; Cyclotrachelus dejeanellus (Csiki, 1930) for C. morio (Dejean, 1828); Cyclotrachelus freitagi Bousquet, new replacement name for C. obsoletus (Say, 1830); Dyschirius aeneolus LeConte, 1850 for D. frigidus Mannerheim, 1853; Harpalus laevipes Zetterstedt, 1828 for H. quadripunctatus Dejean, 1829; Harpalus providens Casey, 1914 for H. viduus LeConte, 1865; Harpalus reversus Casey, 1924 for H. funerarius Csiki, 1932; Notiophilus sierranus Casey, 1920 for N. obscurus Fall, 1901; Pseudamara Lindroth, 1968 for Disamara Lindroth, 1976; Pterostichus trinarius (Casey, 1918) for P. ohionis Csiki, 1930; Stenolophus carbo Bousquet, new replacement name for S. carbonarius (Dejean, 1829).Thirty-six new synonyms are established and seven, considered as questionable, are confirmed. They are (with the valid names in parentheses): Agonothorax planipennis Motschulsky, 1850 (= ? Agonum affine Kirby, 1837); Platynus variolatus LeConte, 1851 (= Agonum limbatum Motschulsky, 1845); Agonum nitidum Harris, 1869 (= ? Agonum melanarium Dejean, 1828); Amerinus fuscicornis Casey, 1914 and A. longipennis Casey, 1914 (= Amerinus linearis (LeConte, 1863)); Apristus fuscipennis Motschulsky, 1864 (= Apristus latens LeConte, 1848); Batenus aeneolus Motschulsky, 1865 (= Agonum exaratum (Mannerheim, 1853)); Brachystylus curtipennis Motschulsky, 1859 (= Pterostichus congestus (Ménétriés, 1843)); Brachystylus parallelus Motschulsky, 1859 (= ? Pterostichus californicus (Dejean, 1828)); Cratacanthus cephalotes Casey, 1914, C. subovalis Casey, 1914, and C. texanus Casey, 1884 (= Cratacanthus dubius (Palisot de Beauvois, 1811)); Cymindis comma T.W. Harris, 1869 (= ? Cymindis limbatus Dejean, 1831); Feronia praetermissa Chaudoir, 1868 (= Pterostichus commutabilis (Motschulsky, 1866)); Galerita angusticeps Casey, 1920 (= Galerita janus (Fabricius, 1792)); Gonoderus cordicollis Motschulsky 1859 (= Pterostichus tristis (Dejean, 1828)); Anisodactylus alternans LeConte, 1851 (= Anisodactylus alternans (Motschulsky, 1845)); Hypherpes spissitarsis Casey, 1918 (= Pterostichus tarsalis LeConte, 1873); Lebia brunnicollis Motschulsky, 1864 (= Lebia lobulata LeConte, 1863); Lebia subfigurata Motschulsky, 1864 and L. sublimbata Motschulsky, 1864 (= Lebia analis Dejean, 1825); Lophoglossus bispiculatus Casey, 1913 and L. illini Casey, 1913 (= Lophoglossus scrutator (LeConte, 1848)); Platysma leconteianum Lutshnik, 1922 (= Pterostichus commutabilis (Motschulsky, 1866)); Loxandrus iris Motschulsky, 1866(= Loxandrus rectus (Say, 1823)); Masoreus americanus Motschulsky, 1864 (= Stenolophus rotundicollis (Haldeman, 1843)); Notaphus laterimaculatus Motschulsky, 1859 (= Bembidion approximatum (LeConte, 1852)); Notiophilus cribrilaterus Motschulsky, 1864 (= Notiophilus novemstriatus LeConte, 1848); Omaseus brevibasis Casey, 1924 (= Pterostichus luctuosus (Dejean, 1828)); Notaphus incertus Motschulsky, 1845 (= Bembidion breve (Motschulsky, 1845)); Peryphus concolor Motschulsky, 1850 (= Bembidion platynoides Hayward, 1897); Peryphus erosus Motschulsky, 1850 (= Bembidion transversale Dejean, 1831); Peryphus subinflatus Motschulsky, 1859 (= Bembidion petrosum petrosum Gebler, 1833); Planesus fuscicollis Motschulsky, 1865 and P. laevigatas Motschulsky, 1865 (= Cymindis platicollis (Say, 1823)); Poecilus pimalis Casey, 1913 (= Poecilus diplophryus Chaudoir, 1876); Pterostichus arizonicus Schaeffer, 1910 (= Ophryogaster flohri Bates, 1882); Pterostichus sequoiarum Casey, 1913 (= Pterostichus tarsalis LeConte, 1873); Scaphinotus grandis Gistel, 1857 (= ? Scaphinotus unicolor unicolor (Fabricius, 1787)); Stenocrepis chalcas Bates, 1882 and S. chalcochrous Chaudoir, 1883 (= Stenocrepis texana (LeConte, 1863)); Stenolophus humeralis Motschulsky, 1864 (= Stenolophus plebejus Dejean, 1829); and Stenolophus laticollis Motschulsky, 1864 (= Stenolophus ochropezus (Say, 1823)).Olisthopus iterans Casey, 1913 and Pterostichus illustris LeConte, 1851, listed as junior synonyms of O. parmatus (Say, 1823) and P. congestus (Ménétriés, 1843), respectively, are considered in the present work as valid species.The type species (listed in parentheses) of the following 14 genus-group taxa are designated for the first time: Circinalidia Casey, 1920 (Agonum aeruginosum Dejean, 1828); Evolenes LeConte, 1853 (Oodes exaratus Dejean, 1831); Leucagonum Casey, 1920 (Agonum maculicolle Dejean, 1828); Megaliridia Casey, 1920 (Cychrus viduus Dejean, 1826); Megalostylus Chaudoir, 1843 (Feronia lucidula Dejean, 1828 = Feronia recta Say, 1823); Micragra Chaudoir, 1872 (Micragra lissonota Chaudoir, 1872); Onota Chaudoir, 1872 (Onota bicolor Chaudoir, 1872); Oodiellus Chaudoir, 1882 (Oodiellus mexicanus Chaudoir, 1882 = Anatrichis alutacea Bates, 1882); Oxydrepanus Putzeys, 1866 (Dyschirius rufus Putzeys, 1846); Paranchomenus Casey, 1920 (Platynus stygicus LeConte, 1854 = Anchomenus mannerheimii Dejean, 1828); Pemphus Motschulsky, 1866 (Cychrus velutinus Ménétriés, 1843); Peronoscelis Chaudoir, 1872 (Tetragonoderus figuratus Dejean, 1831); Rhombodera Reiche, 1842 (Rhombodera virgata Reiche, 1842 = Lebia trivittata Dejean, 1831); and Stenous Chaudoir, 1857 (Oodes cupreus Chaudoir, 1843).Two new family-group names are proposed, Cnemalobini (= Cnemacanthini of authors) based on Cnemalobus Guérin-Méneville, 1839 and Loxandrini based on Loxandrus LeConte, 1852.The work also includes a synopsis of all extant world carabid tribes, a bibliography of all original descriptions, a full taxonomic index, and, as appendices, lists of nomina nuda and unjustified emendations, and annotated lists of species incorrectly or doubtfully recorded from America north of Mexico and of new North American records.

BackgroundThe NHS English Quality Premium recommends that inappropriate antibiotic prescribing is reduced; there are a range of national antimicrobial stewardship (AMS) initiatives to support this.AimThe aim of this study is to assess AMS activities in primary care across England. The findings will be used to inform how the RCGP, PHE and NHS can help optimise stewardship activities.MethodQualitative interviews: with AMS leads within Clinical Commissioning Groups’ (CCGs) and Commissioning Support Units’ (CSUs) medicines management teams. Questionnaire: informed by the qualitative data, sent to all 209 CCGs in England in 2017.ResultsIn total, 89% (187/209) of CCGs returned a questionnaire; 82% of AMS leads reported spending only 0.1 whole-time equivalent on AMS activities, as it was only one role within a wider remit, so dedicating time is challenging. 99% (167/169) of CCGs had delivered AMS education in the last 2 years: 140 face-to-face; 121 via e-learning. 99% (184/186) actively promoted the TARGET Antibiotics Toolkit; 94% (175/187) actively promoted TARGET patient leaflets: 92% The Treating Your Infection (TYI) leaflet. 90% (166/185) used the PHE managing common infections guidance: 81% (149/185) modify or localise; 41/185 (22%) signpost directly to it. Eighty-six CCGs reported using CCG audit tools and 82 CCGs reported using TARGET’s audit tools. 85% (142/168) fed back antimicrobial prescribing data to the CCG/CSU board; 100% (169/169) to general practices and 33% (56/169) to out-of-hours providers.ConclusionAlthough CCGs reported promoting these AMS activities, there was little evaluation of uptake by primary care practitioners. Future work should focus on measuring AMS uptake; having staff dedicated solely to AMS could facilitate this.

Background: Adequate nutrition during infancy and early childhood is essential to ensure the growth, health, and development of children to their full potential. Complementary feeding is a process starting when breast milk alone is no longer sufficient to meet the nutritional requirements of infants, and therefore other foods and liquids are needed, along with breast milk. The objective was to study complementary feeding practices and the various factors influencing them in urban and rural areas.Methods: A community based cross sectional study was conducted in Urban and Rural area of Mangalore Taluk. Data was collected by interview method among 408 mothers using a predesigned pretested questionnaire, information regarding demographic profile, socio-economic status, complementary feeding practices, etc was collected.Results: As many as 186 (45.3%) i.e., 129/186 (69.3%) mothers in the rural area and 57/186 (30.6%) mothers in urban area started complementary feeds at the age of 6 months. The most common food preferred as complementary food was combination of rice and dal together. The number of meals per day given to the child varied from 2-4/day. The number of snacks given per day to the child varied from 1-4 /day; commonly preferred snacks were Biscuits both in urban and rural areas Bottle feeding was practiced by 181 (44.4%) of the mothers, that included 113/181 (62.4%) from rural area and 68/181 (37.5%) from urban area.Conclusions: Poor complementary feeding practices were observed both in rural and urban areas. Family member’s advice, poor knowledge and influence of baby food marketing strategies have resulted in inappropriate practices.

In this study, we tested the hypothesis that MCI-186 (3-methyl-1-phenyl-2-pyrazolin-5-one; edaravone), a novel free radical scavenger, protects against acute experimental autoimmune myocarditis (EAM) in rats by the radical scavenging action associated with the suppression of cytotoxic myocardial injury. Recent evidence suggests that oxidative stress may play a role in myocarditis. We administered MCI-186 intraperitoneally at 1, 3, and 10 mg·kg−1·day−1 to rats with EAM for 3 wk. The results were compared with untreated rats with EAM. MCI-186 treatment did not affect hemodynamics. MCI-186 treatment (3 and 10 mg·kg−1·day−1) reduced the severity of myocarditis as assessed by comparing the heart-to-body weight ratio and pathological scores. Myocardial interleukin-1β (IL-1β)-positive cells and myocardial oxidative stress overload with DNA damage in rats with EAM given MCI-186 treatment were significantly less compared with those of the untreated rats with EAM. In addition, MCI-186 treatment decreased not only the myocardial protein carbonyl contents but also the myocardial thiobarbituric acid reactive substance products in rats with EAM. The formation of hydroxyl radicals in MCI-186-treated heart homogenates was decreased compared with untreated heart homogenates. Furthermore, cytotoxic activities of lymphocytes of rats with EAM treated with MCI-186 were significantly lower compared with those of the untreated rats with EAM. Hydroxyl radicals may be involved in the development of myocarditis. MCI-186 protects against acute EAM in rats associated with scavenging hydroxyl free radicals, resulting in the suppression of autoimmune-mediated myocardial damage associated with reduced oxidative stress state.

The aim of this study is to illustrate the biofunctions of miRNA-186-5p level in breast cancer (BCa) and to explore the underlying mechanisms. Levels of miRNA-186-5p in BCa tissues and adjacent normal ones were determined. Association of miRNA-186-5p with pathological parameters and prognosis in BCa patients was analyzed. Luciferase assay was conducted for the prediction of the interaction between miRNA-186-5p and CXCL13. Their mutual interaction in influencing the proliferative potential of BCa was finally explored. Results showed that miRNA-186-5p expression was downregulated in BCa cell lines and tissues. MiRNA-186-5p overexpression could attenuate proliferative ability in BCa cells. A direct and negative correlation was identified between miRNA-186-5p and CXCL13. In addition, their mutual interaction was coresponsible for the malignant development of BCa. In BCa patients, miRNA-186-5p level was remarkably associated with tumor size and tumor staging, rather than other pathological parameters. Low level of miRNA-186-5p predicted a poor prognosis in BCa. Downregulated miRNA-186-5p in BCa is linked to tumor size, tumor staging, and prognosis. miRNA-186-5p downregulates CXCL13 by binding CXCL13 3′UTR in BCa cells. Overexpression of CXCL13 can significantly neutralize the inhibitory effects of miRNA-186-5p on BCa proliferation.

This study analyzes the context of space, knowledge and school time present in the public and private education reports of the province of Alagoas, written by the physician Thomaz do Bomfim Espindola (1832-1889) in the 19th century. These reports were the result of his role as Inspector General of Studies in the years 1866 to 1868. These writings include themes such as poor teacher qualifications, poor application of learning methods, abandonment of physical education, moral education, and religious education. quantitative figures on the number of private and public primary and secondary schools, teacher hiring, replacement and dismissal, among other subjects. As a member of the Liberal Party of Alagoas, Espindola held the positions of provincial deputy from 1860-1861, 1864-1865 and 1866-1867, deputy general from 1878 to 1881 and from 1881 to 1884, and interim president in the same province in 1867 and 1878. In Education, he worked as a teacher of Geography, Chronology and History at the Alagoas High School, Hygiene at the High School of Arts and Crafts and Philosophy at São Bernardo High School. He was consulted to propose changes in Brazilian education by drafting the opinions of the «Reform of Primary Education and Various Complementary Institutions of Public Education» (1882) and the «Reform of Secondary and Higher Education» (1883) together with Rui Barbosa and Ulysses Vianna. Therefore, the analysis of the theoretical relationships of space, knowledge and school time of public and private education in the province of Alagoas contributes to the understanding of the advances and the limits of the school formation of the Brazilian Empire.

Abstract Background This study compares the detection of respiratory pathogens between a multitest “Bundle” (MTB) and the Sputum FilmArray Pneumonia Panel (SFAPP). Methods Patients admitted from the ED with CAP were enrolled. The SFAPP probed for the presence of 18 bacterial species and 17 viral targets. The results were compared with pathogen detection with an MTB: (a) culture of sputum and blood; (b) urine antigens of S. pneumoniae and Legionella pneumophila; (c) Nasopharyngeal (NP) Respiratory FilmArray (NPRFA) panel which detects 17 viruses and 3 bacteria; and (d) nasal NAATs for S. pneumoniae and S. aureus. Two serum procalcitonin (PCT) levels helped separate bacterial colonization from invasion. Results Of 400 enrolled patients, 121 (30%) were non-evaluable due to a lack of a sputum specimen, 72 (18%) with a final diagnosis other than CAP, and other reasons in 21 (5%). Herein, the results of 186 (47%) evaluable patients with CAP and the Pneumonia Severity Index values of over 90 in 64.5%. The SFAPP detected viruses in 114/186 (61.3%) patients compared with 73/186 (39.2%) with the NPRFAP, p. The SFAPP detected bacterial pathogen(s) in 140/186 (75.3%) of patients vs. 117/183 (62.9%) with the MTB, pH. influenzae, M. catarrhalis, and S. agalactiae, p. A potential pathogenic bacteria and/or virus was detected in 176 of the 186 (95%) evaluable patients. Patients were classified as: virus detected (22); bacteria detected (57); bacteria and virus (97); CAP but no pathogen detected (10). The distribution of serum PCT levels by pathogen detected is shown in Figure 1. The dashed line is the 0.25 ng/mL “cut-off” to help separate colonization from invasion by bacteria. Antibiotic use was less in influenza patients with low PCT levels, p. In 22 patients with only virus detected and PCT. Conclusion The Sputum FilmArray Pneumonia Panel detected more bacteria and viral potential pathogens than the Multitest Bundle that included the Nasopharyngeal FilmArray Panel. The Sputum FilmArray Pneumonia Panel may allow removal of nasopharyngeal swabs and urine antigens from the MTB. Disclosures All authors: No reported disclosures.

Purpose: The spectrum of diagnoses and clinical features of hand tumors differ from those of tumors in other body parts. However, only a few reports have comprehensively referenced the diagnosis and clinical features of hand tumors. This study aimed to elucidate the diagnostic distribution and the clinical features of hand tumors undergone surgery in our institute. Patients and methods: A total of 235 lesions in 186 patients diagnosed with hand tumors between 1978 and 2020 were reviewed. Age at surgery, gender, chief complaint, tumor location, and pathological diagnosis were analyzed. Results: There were 121 benign bone tumors, 98 benign soft tissue tumors, and 16 malignant tumors. Chondroma and tenosynovial giant cell tumor were common benign bone and soft tissue tumors at the proximal phalanx of the ring finger and the palm, respectively. Meanwhile, chondrosarcoma and synovial sarcoma were common malignant tumors at the dorsal part of the hand. Local pain and painless mass were the chief complaints in patients with benign bone and soft tissue tumors, respectively. Most patients with malignant tumors were referred after unplanned resection. When patients were classified into two categories by tumor size according to maximal diameter, tumors larger than 19 mm had a significantly higher risk of malignant ( p = 0.031) despite being smaller than other tumors in different body parts. Conclusion: When a tumor malignancy is suspected, the patient should be referred to a specialist to avoid unplanned resection or delayed diagnosis due to misdiagnosis. Knowing the distribution and clinical features should help in diagnosing hand tumors.

Resumo: Trata-se analisar a Ação por Descumprimento de Preceito Fundamental (ADPF) n.186. Tal ação, movida pelo partido Democratas em 2009, pedia que o Supremo Tribunal Federal declarasse como inconstitucional a medida tomada pela Universidade de Brasília que estabelecia uma reserva de 20% das vagas com base no critério étnico-racial. O objetivo desta análise é identificar o principal argumento utilizado pela Corte Constitucional para declarar a constitucionalidade do referido critério. Tendo como referência os votos dos Ministros do Supremo Tribunal Federal, conclui-se que o princípio da igualdade material é o fundamento da decisão que declara constitucional a reserva de vagas para negros e pardos no que tange ao acesso ao ensino superior.Palavras-chave: Ações afirmativas; Constitucionalidade; Igualdade Material.

The present study aimed to investigate the effect of miR-186 on proliferation, migration, invasion, and epithelialmesenchymal transition (EMT) of hepatocellular carcinoma (HCC). In this work, miR-186 was downregulated in HCC tissues and cells, and low miR-186 level helped predict the occurrence of vascular invasion and poor prognosis in patients with HCC. miR-186 overexpression inhibited cell proliferation and tumor growth in nude mice, repressed migration and invasion abilities, and enhanced apoptosis in HCC cells. miR-186 also retarded progression of EMT. miR-186 directly bound to the 3-untranslated regions of cyclin-dependent kinase 6 (CDK6) to inhibit its expression. Overexpression of CDK6 markedly reversed inhibitory effects of miR-186 on proliferation, apoptosis, migration, and invasion of HCC cells. Conversely, inhibition of CDK6 exerted synergic effect on the biological functions of miR-186. In conclusion, miR-186 represses proliferation, migration, invasion, and EMT, and induces apoptosis through targeting CDK6 in HCC, which may provide a new therapeutic target for HCC.

- Francesco Benigno e Daniele Di Bartolomeo, Napoleone deve morire. L'idea di ripetizione storica nella Rivoluzione francese, Roma, Salerno, 2020, 194 p. br/> - Salvatore Santuccio, Uno stato nello stato. Sette segrete, complotti e rivolte nella Sicilia di primo Ottocento, Acireale, Bonanno, 2020, 301 p.- Enrico Francia, Oggetti risorgimentali. Una storia materiale della politica nel primo Ottocento, Roma, Carocci, 2021, 180 p.- Jacopo De Santis, Tra altari e barricate. La vita religiosa a Roma durante la Repubblica romana del 1849, Firenze, Firenze University Press, 2021, 282 p.- Giampaolo Conte, Il credito di una nazione. Politica, diplomazia e società di fronte al problema del debito pubblico italiano. 1861-1876, Roma, Edizioni di Storia e Letteratura, 2021, 114 p. - Massimo Baioni, Vedere per credere. Il racconto museale dell'Italia unita, Roma, Viella, 2020, 266 p.- Gabriele B. Clemens, Geschichte des Risorgimento. Italiens Weg in die Moderne (1770-1870), Wien-Köln, Böhlau, 2021, 264 p.- Du "Grand Tour" au Traité de Rome: l'Europe au bout du voyage, sous la direction de Francis Démier et Elena Musiani, Rennes, Presses universitaires, 2021, 186 p.

Deregulation of miR-186 and Twist1 has been identified to be involved in the progression of multiple cancers. However, the detailed molecular mechanisms underlying miR-186-involved cholangiocarcinoma (CCA) are still unknown. In this study, we found that miR-186 was downregulated in CCA tissues and cell lines, and negatively correlated with the expression of Twist1 protein. In vitro assays demonstrated that miR-186 mimics repressed cell proliferation, in vivo tumor formation, and caused cell cycle arrest. miR-186 mimics also inhibited the migration and invasion of CCLP1 and SG-231 cells. Mechanistically, the 3′-untranslated region (3′-UTR) of Twist1 mRNA is a direct target of miR-186. Further, miR-186 inhibited the expressions of Twist1, N-cadherin, vimentin, and matrix metallopeptidase 9 (MMP9) proteins, whereas it increased the expression of E-cadherin in CCLP1 and SG-231 cells. Silencing of Twist1 expression enhanced the inhibitory effects of miR-186 on the proliferation, migration, and invasion of CCLP1 and SG-231 cells. In conclusion, miR-186 inhibited cell proliferation, migration, invasion, and epithelial‐mesenchymal transition (EMT) through targeting Twist1 in human CCA. Thus, miR-186/Twist1 axis may benefit the development of therapies for CCA.

Purpose: To investigate the suppressive influence of mir-186 on multiplication and growth of multiple myeloma (MM), as well as the processes involved.Methods: The U266 cells were divided into control, mir-186 overexpression, and inhibition groups. The latter two were transfected with mir-186 agent and antagonist, respectively. Cell viability, colony formation potential, cell cycle ratio, and Jagged-1 mRNA and protein levels were measured using various assays.Results: Cell growth increased over time in all groups. However, mir-186 overexpression cells showed significantly decreased growth and colony formation capacity, relative to control, while the mir-186 inhibition cells showed significantly higher growth and colony formation capacity. The study revealed a higher proportion of G0/G1 stage cells and lower proportion of S-phase cells in mir-186 overexpression cells than in control cells. The opposite effect was seen in mir-186 inhibition cells. Jagged-1 protein and mRNA levels were significantly lower in mir-186 overexpression cells and higher in mir-186 inhibition cells than in control group. The Jagged-1 knockout group showed significantly higher Jagged-1 mRNA and protein levels than both the control and mir-186 overexpression groups (p < 0.05).Conclusion: When overexpressed, mir-186 inhibits the growth of multiple myeloma cells by inhibiting cell colony-formation capacity and by regulating cell cycle through mir-186-induced regulation of the expression of Jagged-1. there is need for more research to confirm the clinical benefits of therapies based on these findings.

The aims of the present research were to study selection samples of cocksfoot in the conditions of the middle taiga zone of the Komi Republic with the ecological adaptability parameters, calculated on the basis of green mass yield, with a subsequent selection of the most promising forms for further breeding. The experimental part of the work was carried out in the breeding nurseries laid on the experimental fields of the A.V. Zhuravsky Institute of Agrobiotechnologies FRC Komi SC UB RAS (Syktyvkar) in 2019-2021. We studied 7 cross-pollinated lines from wild-growing populations from the Komi Republic (BN-184, BN-185, BN-186, BN-188), Norway (BN-1817) and Finland (BN-1816) which were given breeding numbers (BNs). Since there were no locally recognized varieties during the study period, BN-1810 was taken as a control. Agroclimatic conditions during the years of research varied. By the environmental conditions’ index, 2020 saw favorable growing conditions (Ij = +14.2) and 2019 – relatively unfavorable (Ij = -18.4). The average yield of green mass of cocksfoot ranged within 22.6-30.3 t/ha in 2019-2021. BN-188 demonstrated the highest result (30.3 t/ha). Almost any breeding number showed a high ecological adaptability: the plasticity coefficient varied within 0.91-1.09. BN-1810, BN-185, BN-184, BN-1816 turned out to be highly adaptive and flexible (bi=1.00-1.09, Si2=0.25-0.75). BN-188 (125.5 %) and BN-185 (115.2 %) were marked through the highest stability level of variety. These numbers also were first by the stability index (0.50 and 0.47, respectively). Four of the studied breeding numbers had the adaptability coefficient of 1.03-1.12 with the highest value of BN-188. The greatest genetic flexibility between genotype and environmental factors was noted for BN-188 (18.1), as well as for BN-185 (17.5), BN-1810 (17.5) and BN-1816 (17.6). BN-185 (Sc=6.9) and BN-188 (Sc=6.4) are classified as having the highest breeding value. In total, according to the set of adaptability parameters, the breeding numbers BN-188 and BN-185 were recognized as highly promising forms by the breeding value (Sc = 6.4 and 6.9, respectively), stable productivity, and homeostatic index (Hom. = 1.4).

Objectives MicroRNAs (miRNAs) have been reported as key regulators of bone formation, signalling, and repair. Fracture healing is a proliferative physiological process where the body facilitates the repair of a bone fracture. The aim of our study was to explore the effects of microRNA-186 (miR-186) on fracture healing through the bone morphogenetic protein (BMP) signalling pathway by binding to Smad family member 6 (SMAD6) in a mouse model of femoral fracture. Methods Microarray analysis was adopted to identify the regulatory miR of SMAD6. 3D micro-CT was performed to assess the bone volume (BV), bone volume fraction (BVF, BV/TV), and bone mineral density (BMD), followed by a biomechanical test for maximum load, maximum radial degrees, elastic radial degrees, and rigidity of the femur. The positive expression of SMAD6 in fracture tissues was measured. Moreover, the miR-186 level, messenger RNA (mRNA) level, and protein levels of SMAD6, BMP-2, and BMP-7 were examined. Results MicroRNA-186 was predicted to regulate SMAD6. Furthermore, SMAD6 was verified as a target gene of miR-186. Overexpressed miR-186 and SMAD6 silencing resulted in increased callus formation, BMD and BV/TV, as well as maximum load, maximum radial degrees, elastic radial degrees, and rigidity of the femur. In addition, the mRNA and protein levels of SMAD6 were decreased, while BMP-2 and BMP-7 levels were elevated in response to upregulated miR-186 and SMAD6 silencing. Conclusion In conclusion, the study indicated that miR-186 could activate the BMP signalling pathway to promote fracture healing by inhibiting SMAD6 in a mouse model of femoral fracture. Cite this article: Bone Joint Res 2019;8:550–562.

More than 4700 nominal family-group names (including names for fossils and ichnotaxa) are nomenclaturally available in the order Coleoptera. Since each family-group name is based on the concept of its type genus, we argue that the stability of names used for the classification of beetles depends on accurate nomenclatural data for each type genus. Following a review of taxonomic literature, with a focus on works that potentially contain type species designations, we provide a synthesis of nomenclatural data associated with the type genus of each nomenclaturally available family-group name in Coleoptera. For each type genus the author(s), year of publication, and page number are given as well as its current status (i.e., whether treated as valid or not) and current classification. Information about the type species of each type genus and the type species fixation (i.e., fixed originally or subsequently, and if subsequently, by whom) is also given. The original spelling of the family-group name that is based on each type genus is included, with its author(s), year, and stem. We append a list of nomenclaturally available family-group names presented in a classification scheme. Because of the importance of the Principle of Priority in zoological nomenclature, we provide information on the date of publication of the references cited in this work, when known. Several nomenclatural issues emerged during the course of this work. We therefore appeal to the community of coleopterists to submit applications to the International Commission on Zoological Nomenclature (henceforth “Commission”) in order to permanently resolve some of the problems outlined here. The following changes of authorship for type genera are implemented here (these changes do not affect the concept of each type genus): CHRYSOMELIDAE: Fulcidax Crotch, 1870 (previously credited to “Clavareau, 1913”); CICINDELIDAE: Euprosopus W.S. MacLeay, 1825 (previously credited to “Dejean, 1825”); COCCINELLIDAE: Alesia Reiche, 1848 (previously credited to “Mulsant, 1850”); CURCULIONIDAE: Arachnopus Boisduval, 1835 (previously credited to “Guérin-Méneville, 1838”); ELATERIDAE: Thylacosternus Gemminger, 1869 (previously credited to “Bonvouloir, 1871”); EUCNEMIDAE: Arrhipis Gemminger, 1869 (previously credited to “Bonvouloir, 1871”), Mesogenus Gemminger, 1869 (previously credited to “Bonvouloir, 1871”); LUCANIDAE: Sinodendron Hellwig, 1791 (previously credited to “Hellwig, 1792”); PASSALIDAE: Neleides Harold, 1868 (previously credited to “Kaup, 1869”), Neleus Harold, 1868 (previously credited to “Kaup, 1869”), Pertinax Harold, 1868 (previously credited to “Kaup, 1869”), Petrejus Harold, 1868 (previously credited to “Kaup, 1869”), Undulifer Harold, 1868 (previously credited to “Kaup, 1869”), Vatinius Harold, 1868 (previously credited to “Kaup, 1869”); PTINIDAE: Mezium Leach, 1819 (previously credited to “Curtis, 1828”); PYROCHROIDAE: Agnathus Germar, 1818 (previously credited to “Germar, 1825”); SCARABAEIDAE: Eucranium Dejean, 1833 (previously “Brullé, 1838”). The following changes of type species were implemented following the discovery of older type species fixations (these changes do not pose a threat to nomenclatural stability): BOLBOCERATIDAE: Bolbocerus bocchus Erichson, 1841 for Bolbelasmus Boucomont, 1911 (previously Bolboceras gallicum Mulsant, 1842); BUPRESTIDAE: Stigmodera guerinii Hope, 1843 for Neocuris Saunders, 1868 (previously Anthaxia fortnumi Hope, 1846), Stigmodera peroni Laporte & Gory, 1837 for Curis Laporte & Gory, 1837 (previously Buprestis caloptera Boisduval, 1835); CARABIDAE: Carabus elatus Fabricius, 1801 for Molops Bonelli, 1810 (previously Carabus terricola Herbst, 1784 sensu Fabricius, 1792); CERAMBYCIDAE: Prionus palmatus Fabricius, 1792 for Macrotoma Audinet-Serville, 1832 (previously Prionus serripes Fabricius, 1781); CHRYSOMELIDAE: Donacia equiseti Fabricius, 1798 for Haemonia Dejean, 1821 (previously Donacia zosterae Fabricius, 1801), Eumolpus ruber Latreille, 1807 for Euryope Dalman, 1824 (previously Cryptocephalus rubrifrons Fabricius, 1787), Galeruca affinis Paykull, 1799 for Psylliodes Latreille, 1829 (previously Chrysomela chrysocephala Linnaeus, 1758); COCCINELLIDAE: Dermestes rufus Herbst, 1783 for Coccidula Kugelann, 1798 (previously Chrysomela scutellata Herbst, 1783); CRYPTOPHAGIDAE: Ips caricis G.-A. Olivier, 1790 for Telmatophilus Heer, 1841 (previously Cryptophagus typhae Fallén, 1802), Silpha evanescens Marsham, 1802 for Atomaria Stephens, 1829 (previously Dermestes nigripennis Paykull, 1798); CURCULIONIDAE: Bostrichus cinereus Herbst, 1794 for Crypturgus Erichson, 1836 (previously Bostrichus pusillus Gyllenhal, 1813); DERMESTIDAE: Dermestes trifasciatus Fabricius, 1787 for Attagenus Latreille, 1802 (previously Dermestes pellio Linnaeus, 1758); ELATERIDAE: Elater sulcatus Fabricius, 1777 for Chalcolepidius Eschscholtz, 1829 (previously Chalcolepidius zonatus Eschscholtz, 1829); ENDOMYCHIDAE: Endomychus rufitarsis Chevrolat, 1835 for Epipocus Chevrolat, 1836 (previously Endomychus tibialis Guérin-Méneville, 1834); EROTYLIDAE: Ips humeralis Fabricius, 1787 for Dacne Latreille, 1797 (previously Dermestes bipustulatus Thunberg, 1781); EUCNEMIDAE: Fornax austrocaledonicus Perroud & Montrouzier, 1865 for Mesogenus Gemminger, 1869 (previously Mesogenus mellyi Bonvouloir, 1871); GLAPHYRIDAE: Melolontha serratulae Fabricius, 1792 for Glaphyrus Latreille, 1802 (previously Scarabaeus maurus Linnaeus, 1758); HISTERIDAE: Hister striatus Forster, 1771 for Onthophilus Leach, 1817 (previously Hister sulcatus Moll, 1784); LAMPYRIDAE: Ototreta fornicata E. Olivier, 1900 for Ototreta E. Olivier, 1900 (previously Ototreta weyersi E. Olivier, 1900); LUCANIDAE: Lucanus cancroides Fabricius, 1787 for Lissotes Westwood, 1855 (previously Lissotes menalcas Westwood, 1855); MELANDRYIDAE: Nothus clavipes G.-A. Olivier, 1812 for Nothus G.-A. Olivier, 1812 (previously Nothus praeustus G.-A. Olivier, 1812); MELYRIDAE: Lagria ater Fabricius, 1787 for Enicopus Stephens, 1830 (previously Dermestes hirtus Linnaeus, 1767); NITIDULIDAE: Sphaeridium luteum Fabricius, 1787 for Cychramus Kugelann, 1794 (previously Strongylus quadripunctatus Herbst, 1792); OEDEMERIDAE: Helops laevis Fabricius, 1787 for Ditylus Fischer, 1817 (previously Ditylus helopioides Fischer, 1817 [sic]); PHALACRIDAE: Sphaeridium aeneum Fabricius, 1792 for Olibrus Erichson, 1845 (previously Sphaeridium bicolor Fabricius, 1792); RHIPICERIDAE: Sandalus niger Knoch, 1801 for Sandalus Knoch, 1801 (previously Sandalus petrophya Knoch, 1801); SCARABAEIDAE: Cetonia clathrata G.-A. Olivier, 1792 for Inca Lepeletier & Audinet-Serville, 1828 (previously Cetonia ynca Weber, 1801); Gnathocera vitticollis W. Kirby, 1825 for Gnathocera W. Kirby, 1825 (previously Gnathocera immaculata W. Kirby, 1825); Melolontha villosula Illiger, 1803 for Chasmatopterus Dejean, 1821 (previously Melolontha hirtula Illiger, 1803); STAPHYLINIDAE: Staphylinus politus Linnaeus, 1758 for Philonthus Stephens, 1829 (previously Staphylinus splendens Fabricius, 1792); ZOPHERIDAE: Hispa mutica Linnaeus, 1767 for Orthocerus Latreille, 1797 (previously Tenebrio hirticornis DeGeer, 1775). The discovery of type species fixations that are older than those currently accepted pose a threat to nomenclatural stability (an application to the Commission is necessary to address each problem): CANTHARIDAE: Malthinus Latreille, 1805, Malthodes Kiesenwetter, 1852; CARABIDAE: Bradycellus Erichson, 1837, Chlaenius Bonelli, 1810, Harpalus Latreille, 1802, Lebia Latreille, 1802, Pheropsophus Solier, 1834, Trechus Clairville, 1806; CERAMBYCIDAE: Callichroma Latreille, 1816, Callidium Fabricius, 1775, Cerasphorus Audinet-Serville, 1834, Dorcadion Dalman, 1817, Leptura Linnaeus, 1758, Mesosa Latreille, 1829, Plectromerus Haldeman, 1847; CHRYSOMELIDAE: Amblycerus Thunberg, 1815, Chaetocnema Stephens, 1831, Chlamys Knoch, 1801, Monomacra Chevrolat, 1836, Phratora Chevrolat, 1836, Stylosomus Suffrian, 1847; COLONIDAE: Colon Herbst, 1797; CURCULIONIDAE: Cryphalus Erichson, 1836, Lepyrus Germar, 1817; ELATERIDAE: Adelocera Latreille, 1829, Beliophorus Eschscholtz, 1829; ENDOMYCHIDAE: Amphisternus Germar, 1843, Dapsa Latreille, 1829; GLAPHYRIDAE: Anthypna Eschscholtz, 1818; HISTERIDAE: Hololepta Paykull, 1811, Trypanaeus Eschscholtz, 1829; LEIODIDAE: Anisotoma Panzer, 1796, Camiarus Sharp, 1878, Choleva Latreille, 1797; LYCIDAE: Calopteron Laporte, 1838, Dictyoptera Latreille, 1829; MELOIDAE: Epicauta Dejean, 1834; NITIDULIDAE: Strongylus Herbst, 1792; SCARABAEIDAE: Anisoplia Schönherr, 1817, Anticheira Eschscholtz, 1818, Cyclocephala Dejean, 1821, Glycyphana Burmeister, 1842, Omaloplia Schönherr, 1817, Oniticellus Dejean, 1821, Parachilia Burmeister, 1842, Xylotrupes Hope, 1837; STAPHYLINIDAE: Batrisus Aubé, 1833, Phloeonomus Heer, 1840, Silpha Linnaeus, 1758; TENEBRIONIDAE: Bolitophagus Illiger, 1798, Mycetochara Guérin-Méneville, 1827. Type species are fixed for the following nominal genera: ANTHRIBIDAE: Decataphanes gracilis Labram & Imhoff, 1840 for Decataphanes Labram & Imhoff, 1840; CARABIDAE: Feronia erratica Dejean, 1828 for Loxandrus J.L. LeConte, 1853; CERAMBYCIDAE: Tmesisternus oblongus Boisduval, 1835 for Icthyosoma Boisduval, 1835; CHRYSOMELIDAE: Brachydactyla annulipes Pic, 1913 for Pseudocrioceris Pic, 1916, Cassida viridis Linnaeus, 1758 for Evaspistes Gistel, 1856, Ocnoscelis cyanoptera Erichson, 1847 for Ocnoscelis Erichson, 1847, Promecotheca petelii Guérin-Méneville, 1840 for Promecotheca Guérin- Méneville, 1840; CLERIDAE: Attelabus mollis Linnaeus, 1758 for Dendroplanetes Gistel, 1856; CORYLOPHIDAE: Corylophus marginicollis J.L. LeConte, 1852 for Corylophodes A. Matthews, 1885; CURCULIONIDAE: Hoplorhinus melanocephalus Chevrolat, 1878 for Hoplorhinus Chevrolat, 1878; Sonnetius binarius Casey, 1922 for Sonnetius Casey, 1922; ELATERIDAE: Pyrophorus melanoxanthus Candèze, 1865 for Alampes Champion, 1896; PHYCOSECIDAE: Phycosecis litoralis Pascoe, 1875 for Phycosecis Pascoe, 1875; PTILODACTYLIDAE: Aploglossa sallei Guérin-Méneville, 1849 for Aploglossa Guérin-Méneville, 1849, Colobodera ovata Klug, 1837 for Colobodera Klug, 1837; PTINIDAE: Dryophilus anobioides Chevrolat, 1832 for Dryobia Gistel, 1856; SCARABAEIDAE: Achloa helvola Erichson, 1840 for Achloa Erichson, 1840, Camenta obesa Burmeister, 1855 for Camenta Erichson, 1847, Pinotus talaus Erichson, 1847 for Pinotus Erichson, 1847, Psilonychus ecklonii Burmeister, 1855 for Psilonychus Burmeister, 1855. New replacement name: CERAMBYCIDAE: Basorus Bouchard & Bousquet, nom. nov. for Sobarus Harold, 1879. New status: CARABIDAE: KRYZHANOVSKIANINI Deuve, 2020, stat. nov. is given the rank of tribe instead of subfamily since our classification uses the rank of subfamily for PAUSSINAE rather than family rank; CERAMBYCIDAE: Amymoma Pascoe, 1866, stat. nov. is used as valid over Neoamymoma Marinoni, 1977, Holopterus Blanchard, 1851, stat. nov. is used as valid over Proholopterus Monné, 2012; CURCULIONIDAE: Phytophilus Schönherr, 1835, stat. nov. is used as valid over the unnecessary new replacement name Synophthalmus Lacordaire, 1863; EUCNEMIDAE: Nematodinus Lea, 1919, stat. nov. is used as valid instead of Arrhipis Gemminger, 1869, which is a junior homonym. Details regarding additional nomenclatural issues that still need to be resolved are included in the entry for each of these type genera: BOSTRICHIDAE: Lyctus Fabricius, 1792; BRENTIDAE: Trachelizus Dejean, 1834; BUPRESTIDAE: Pristiptera Dejean, 1833; CANTHARIDAE: Chauliognathus Hentz, 1830, Telephorus Schäffer, 1766; CARABIDAE: Calathus Bonelli, 1810, Cosnania Dejean, 1821, Dicrochile Guérin-Méneville, 1847, Epactius D.H. Schneider, 1791, Merismoderus Westwood, 1847, Polyhirma Chaudoir, 1850, Solenogenys Westwood, 1860, Zabrus Clairville, 1806; CERAMBYCIDAE: Ancita J. Thomson, 1864, Compsocerus Audinet-Serville, 1834, Dorcadodium Gistel, 1856, Glenea Newman, 1842; Hesperophanes Dejean, 1835, Neoclytus J. Thomson, 1860, Phymasterna Laporte, 1840, Tetrops Stephens, 1829, Zygocera Erichson, 1842; CHRYSOMELIDAE: Acanthoscelides Schilsky, 1905, Corynodes Hope, 1841, Edusella Chapuis, 1874; Hemisphaerota Chevrolat, 1836; Physonota Boheman, 1854, Porphyraspis Hope, 1841; CLERIDAE: Dermestoides Schäffer, 1777; COCCINELLIDAE: Hippodamia Chevrolat, 1836, Myzia Mulsant, 1846, Platynaspis L. Redtenbacher, 1843; CURCULIONIDAE: Coeliodes Schönherr, 1837, Cryptoderma Ritsema, 1885, Deporaus Leach, 1819, Epistrophus Kirsch, 1869, Geonemus Schönherr, 1833, Hylastes Erichson, 1836; DYTISCIDAE: Deronectes Sharp, 1882, Platynectes Régimbart, 1879; EUCNEMIDAE: Dirhagus Latreille, 1834; HYBOSORIDAE: Ceratocanthus A. White, 1842; HYDROPHILIDAE: Cyclonotum Erichson, 1837; LAMPYRIDAE: Luciola Laporte, 1833; LEIODIDAE: Ptomaphagus Hellwig, 1795; LUCANIDAE: Leptinopterus Hope, 1838; LYCIDAE: Cladophorus Guérin-Méneville, 1830, Mimolibnetis Kazantsev, 2000; MELOIDAE: Mylabris Fabricius, 1775; NITIDULIDAE: Meligethes Stephens, 1829; PTILODACTYLIDAE: Daemon Laporte, 1838; SCARABAEIDAE: Allidiostoma Arrow, 1940, Heterochelus Burmeister, 1844, Liatongus Reitter, 1892, Lomaptera Gory & Percheron, 1833, Megaceras Hope, 1837, Stenotarsia Burmeister, 1842; STAPHYLINIDAE: Actocharis Fauvel, 1871, Aleochara Gravenhorst, 1802; STENOTRACHELIDAE: Stenotrachelus Berthold, 1827; TENEBRIONIDAE: Cryptochile Latreille, 1828, Heliopates Dejean, 1834, Helops Fabricius, 1775. First Reviser actions deciding the correct original spelling: CARABIDAE: Aristochroodes Marcilhac, 1993 (not Aritochroodes); CERAMBYCIDAE: Dorcadodium Gistel, 1856 (not Dorcadodion), EVODININI Zamoroka, 2022 (not EVODINIINI); CHRYSOMELIDAE: Caryopemon Jekel, 1855 (not Carpopemon), Decarthrocera Laboissière, 1937 (not Decarthrocerina); CICINDELIDAE: Odontocheila Laporte, 1834 (not Odontacheila); CLERIDAE: CORMODINA Bartlett, 2021 (not CORMODIINA), Orthopleura Spinola, 1845 (not Orthoplevra, not Orthopleuva); CURCULIONIDAE: Arachnobas Boisduval, 1835 (not Arachnopus), Palaeocryptorhynchus Poinar, 2009 (not Palaeocryptorhynus); DYTISCIDAE: Ambarticus Yang et al., 2019 and AMBARTICINI Yang et al., 2019 (not Ambraticus, not AMBRATICINI); LAMPYRIDAE: Megalophthalmus G.R. Gray, 1831 (not Megolophthalmus, not Megalopthalmus); SCARABAEIDAE: Mentophilus Laporte, 1840 (not Mintophilus, not Minthophilus), Pseudadoretus dilutellus Semenov, 1889 (not P. ditutellus). While the correct identification of the type species is assumed, in some cases evidence suggests that species were misidentified when they were fixed as the type of a particular nominal genus. Following the requirements of Article 70.3.2 of the International Code of Zoological Nomenclature we hereby fix the following type species (which in each case is the taxonomic species actually involved in the misidentification): ATTELABIDAE: Rhynchites cavifrons Gyllenhal, 1833 for Lasiorhynchites Jekel, 1860; BOSTRICHIDAE: Ligniperda terebrans Pallas, 1772 for Apate Fabricius, 1775; BRENTIDAE: Ceocephalus appendiculatus Boheman, 1833 for Uroptera Berthold, 1827; BUPRESTIDAE: Buprestis undecimmaculata Herbst, 1784 for Ptosima Dejean, 1833; CARABIDAE: Amara lunicollis Schiødte, 1837 for Amara Bonelli, 1810, Buprestis connexus Geoffroy, 1785 for Polistichus Bonelli, 1810, Carabus atrorufus Strøm, 1768 for Patrobus Dejean, 1821, Carabus gigas Creutzer, 1799 for Procerus Dejean, 1821, Carabus teutonus Schrank, 1781 for Stenolophus Dejean, 1821, Carenum bonellii Westwood, 1842 for Carenum Bonelli, 1813, Scarites picipes G.-A. Olivier, 1795 for Acinopus Dejean, 1821, Trigonotoma indica Brullé, 1834 for Trigonotoma Dejean, 1828; CERAMBYCIDAE: Cerambyx lusitanus Linnaeus, 1767 for Exocentrus Dejean, 1835, Clytus supernotatus Say, 1824 for Psenocerus J.L. LeConte, 1852; CICINDELIDAE: Ctenostoma jekelii Chevrolat, 1858 for Ctenostoma Klug, 1821; CURCULIONIDAE: Cnemogonus lecontei Dietz, 1896 for Cnemogonus J.L. LeConte, 1876; Phloeophagus turbatus Schönherr, 1845 for Phloeophagus Schönherr, 1838; GEOTRUPIDAE: Lucanus apterus Laxmann, 1770 for Lethrus Scopoli, 1777; HISTERIDAE: Hister rugiceps Duftschmid, 1805 for Hypocaccus C.G. Thomson, 1867; HYBOSORIDAE: Hybosorus illigeri Reiche, 1853 for Hybosorus W.S. MacLeay, 1819; HYDROPHILIDAE: Hydrophilus melanocephalus G.-A. Olivier, 1793 for Enochrus C.G. Thomson, 1859; MYCETAEIDAE: Dermestes subterraneus Fabricius, 1801 for Mycetaea Stephens, 1829; SCARABAEIDAE: Aulacium carinatum Reiche, 1841 for Mentophilus Laporte, 1840, Phanaeus vindex W.S. MacLeay, 1819 for Phanaeus W.S. MacLeay, 1819, Ptinus germanus Linnaeus, 1767 for Rhyssemus Mulsant, 1842, Scarabaeus latipes Guérin-Méneville, 1838 for Cheiroplatys Hope, 1837; STAPHYLINIDAE: Scydmaenus tarsatus P.W.J. Müller & Kunze, 1822 for Scydmaenus Latreille, 1802. New synonyms: CERAMBYCIDAE: CARILIINI Zamoroka, 2022, syn. nov. of ACMAEOPINI Della Beffa, 1915, DOLOCERINI Özdikmen, 2016, syn. nov. of BRACHYPTEROMINI Sama, 2008, PELOSSINI Tavakilian, 2013, syn. nov. of LYGRINI Sama, 2008, PROHOLOPTERINI Monné, 2012, syn. nov. of HOLOPTERINI Lacordaire, 1868.