Journal articles on the topic '1993 a-182'

- Roger Busser, Sudo Sueo, The Fukuda Doctrine and ASEAN; New dimensions in Japanese Foreign policy. Singapore: Institute of Southeast Asian Studies, 1992. - P.J. Drooglever, C. Fasseur, De Indologen; Ambtenaren voor de Oost 1825-1950. Amsterdam: Bert Bakker, 1993, 552 pp. - Raymond Evans, Tony Swain, A place for strangers; Towards a history of Australian Aboroginal being. Cambridge: Cambridge University Press, 1993, xi + 330 pp. - CH.F. van Fraassen, Leonard Andaya, The world of Maluku; Eastern Indonesia in the early modern period. Honolulu: University of Hawai Press, 1993, ix + 306 pp. - J. van Goor, Lodewijk Wagenaar, Galle VOC-vestiging in Ceylon; Beschrijving van een koloniale samenleving aan de vooravond van de Singalese opstand tegen het Nederlandse gezag, 1760. Amsterdam: De Bataafsche Leeuw, 1994. - Geert Kalshoven, A. Schrevel, Access to Water; A socio-economic study into the practice of irrigation development in Indonesia. Ph.D. thesis, The Hague: The Institute of Social Studies, 1993. - Nico Kaptein, Mohamed Ariff, Islam and the economic development of Southeast Asia; The Islamic Voluntary Sector in Southeast Asia. Singapore: Institute of Southeast Asian Studies,1991.''Islam and the economic development of Southeast Asia; The Muslim private sector in Southeast Asia. Singapore: Institute of Southeast Asian Studies, 1991. - Victor T. King, Alistair Morrison, Fair land Sarawak; Some recollections of an expatriate official. Ithaca, New York: Cornell University (Southeast Asia Program, Studies on Southeast Asia 13), 1993, xiv + 182 pp. - H.A.J. Klooster, Klaus H. Schreiner-Brauch, Nationalismus und Personenkult im indonesischen Geschichtsverständnis. Ph.D. Dissertation, Universität Hamburg, 1993, xxi + 293 pp. - Han Knapen, Mark Cleary, Borneo; Change and development. Singapore, Oxford and New York: Oxford University Press, 1992, x + 271 pp., tables, figures, index., Peter Eaton (eds.) - Sirtjo Koolhof, Christiaan G.F. de Jong, Geesten, goden en getuigen: Geschiedenis van de Nederlandse zending onder de Buginezen en Makassaren in Zuid-Sulawesi (Indonesië). Kampen: Kok, (1991), 338 pp., ills., maps, index. - Margaret Leidelmeijer, G.R. Knight, Colonial production in provincial Java; The sugar industry in Pekalongan-Tegal, 1800-1942. Amsterdam: VU University Press, 1994. (Comparative Asian Studies 13.) - J.J. Ras, M.C. Ricklefs, War, culture and economy in Java 1677-1726; Asian and European Imperialism in the early Kartasura period. Sydney: Asian studies Association of Australia, in association with Allen and Unwin, 1993, xviii + 425 pp. - Corry M.I. van der Sluys, Rosemary Gianno, Semelai culture and Resin technology. Connecticut: The Connecticut Academy of Arts and Sciences, 1990. - Jaap Timmer, Laurence R. Goldman, The culture of coincidence; Accident and absolute liability in Huli. Oxford: Clarendon Press, 1993, xvi + 443 pp.

Career Counseling for Women, W. Bruce Walsh and Samuel H. Osipow (Eds.). Hillsdale, NJ: Erlbaum, 1994. 385 pp. $34.50 (paper). ISBN 0-8058-1401–9. It Could Happen to Anyone: Why Battered Women Stay, Ola W. Barnett and Alyce D. LaViolette. Thousand Oaks, CA: Sage, 1993. 184 pp. $38.00. ISBN: 0-8039-5310–0. Empowering and Healing the Battered Woman, Mary Ann Dutton. New York: Springer, 1992. 202 pp. $28.95. ISBN: 0-8261-7130–3. Breaking Destructive Patterns: Multiple Strategies for Treating Partner Abuse, Janet A. Geller. New York: Free Press, 1992. 182 pp. $27.95. ISBN: 0-02-911605–8. Against Therapy, Jeffrey Moussaieff Masson. Monroe, ME: Common Courage Press, 1988/1994. 340 pp. $15.95. ISBN 1-56751-022–1. Changing Our Minds: Lesbian Feminism and Psychology, Celia Kitzinger and Rachel Perkins. New York: New York University Press, 1993. 216 pp. $14.95. ISBN: 0-8147-4646–2. Cultures of Organizations. Three Perspectives, Joanne Martin. New York: Oxford University Press, 1992. 240 pp. $35.00. ISBN 0-19-507163–8.

A list of Curculionoidea (Nemonychidae, Anthribidae, Rhynchitidae, Attelabidae, Brentidae, Apionidae, Nanophyidae, Brachyceridae, Curculionidae, Erirhinidae, Raymondionymidae, Dryoph-thoridae, Scolytidae, Platypodidae) thus far known from Italy is drawn up, updating that by Abbazzi et al. published in 1995. Distributional data of each species are given for broad regions such as northern, central, southern Italy, Sicily and Sardinia. New synonymies are: Acentrotypus laevigatus (Kirby, 1808) (= A. brunnipes (Boheman, 1839), syn.nov.), Ceutorhynchus talickyi Korotyaev, 1980 (= C. strejceki Dieckmann, 1981, syn. nov.), Ceutorhynchus pallipes Crotch,1866 (= Curculio minutus Reich, 1797 not Drury, [1773], syn. nov.; = Curculio contractus Marsham, 1802 not Fourcroy, 1785, syn. nov.), Dodecastichus consentaneus (Boheman, 1843) (= D. c. latialis (Solari & Solari, 1915), syn. nov.; = D. c. dimorphus (Solari & Solari, 1915), syn. nov.; = D. c. pentricus Di Marco & Osella, 2001, syn. nov.), Dodecastichus dalmatinus (Gyllenhal, 1843) (= D. d. lauri (Stierlin, 1861), syn. nov.), Dodecastichus mastix (Olivier, 1807) (= D. m. perlongus (Solari & Solari, 1915), syn. nov.; = D. m. scabrior (Reitter, 1913), syn. nov.), Dorytomus Germar, 1817 (= D. subgen. Chaetodorytomus Iablokov-Khnzorian, 1970, syn. nov.; = D. subgen. Euolamus Reitter, 1916, syn. nov.; = D. subgen. Olamus Reitter, 1916, syn. nov.), Exapion Bedel, 1887 (= Ulapion Ehret, 1997, syn. nov.), Larinus ursus (Fabricius, 1792) (= L. carinirostris Gyllenhal, 1837, syn. nov.; = L. genei Boheman, 1843, syn. nov.), Lixini Schönherr, 1823 (= Rhinocyllini Lacordaire, 1863, syn. nov.), Metacinops rhinomacer Kraatz, 1862 (= M. calabrus Stierlin, 1892, syn. nov.), Microplontus nigrovittatus (Schultze,1901) (= Ceutorhynchus subfasciatus Chevrolat, 1860 not Schönherr, 1826, syn. nov.), Otiorhynchus amicalis cenomanus Colonnelli & Magnano, nom. nov. (= O. a. lessinicus (Osella, 1983) not O. lessinicus Franz, 1938, syn. nov.), Otiorhynchus anophthalmoides omeros nom. nov. (= O. a. istriensis (F. Solari, 1955) not Germar, 1824, syn. nov.), Otiorhynchus anthracinus (Scopoli, 1763) (= O. calabrus Stierlin, 1880, syn. nov.), Otiorhynchus armadillo (Rossi, 1792) (= O. halbherri Stierlin, 1890, syn. nov.), Otiorhynchus clibbianus Colonnelli & Magnano, nom. nov. (= O. judicariensis (Osella, 1983) not Reitter, 1913, syn. nov.), Otiorhynchus cornicinus Stierlin, 1861 (= Curculio laevigatus Fabricius, 1792 not Paykull, 1792, syn. nov.), Otiorhynchus fortis Rosenhauer, 1847 (= O. fortis valarsae Reitter, 1913, syn. nov.), Otiorhynchus nodosus (O. F. Müller, 1764) (= O. nodosus comosellus Boheman, 1843, syn. nov.; = O. nodosus gobanzi Gredler, 1868, syn. nov.), Otiorhynchus pupillatus Gyllenhal, 1834 (= O. p. angustipennis Stierlin, 1883, syn. nov.; = O. venetus F. Solari, 1947, syn. nov.), Otiorhynchus serradae Colonnelli & Magnano, nom. nov. (= O. carinatus (Osella 1983) not (Paykull, 1792), syn. nov.), Otiorhynchus strigirostris Boheman, 1843 (= O. aterrimus : Di Marco & Osella, 2002 not Boheman, 1843, syn. nov.; = O. calvus Fiori, 1899, syn. nov.), O. sulcatus (Fabricius, 1775) (= O. linearis Stierlin, 1861, syn. nov.), Otiorhynchus tenebricosus (Herbst, 1784) (= O. olivieri Abbazzi & Osella, 1992, syn. nov.), Phrydiuchus augusti Colonnelli, nom. nov. (= Ceuthorrhynchus speiseri Schultze, 1897 not C. speiseri Frivaldszkyi, 1894, syn. nov.), Phyllobius maculicornis Germar, 1824 (= P. m. lucanus Solari & Solari, 1903, syn. nov.), Phyllobius pyri (Linné, 1758) (= P. vespertinus (Fabricius, 1792), syn. nov.), Polydrusus subgen. Chaerodrys Jacquelin du Val, [1854] (= P. subgen. Metadrosus Schilsky, 1910, syn. nov.), Polydrusus subgen. Eudipnus C. G. Thomson, 1859 (= P. subgen. Chrysoyphis Gozis, 1882, syn. nov.; P. subgen. Thomsoneonymus Desbrochers, 1902, syn. nov.), Polydrusus subgen. Eurodrusus Korotyaev & Meleshko, 1997 (= P. subgen. Neoeustolus Alonso-Zarazaga & Lyal, 1999, syn. nov.), Polydrusus armipes Brullé, 1832 (= P. a. faillae Desbrochers, 1859, syn. nov.), Pseudomyllocerus invreae invreae (F. Solari, 1948) (= Curculio cinerascens Fabricius, 1792 not [Gmelin], 1790], syn. nov. ), Zacladus Reitter, 1916 (= Z. subgen. Amurocladus Korotyaev, 1997, syn. nov.; = Z. subgen. Angarocladus Korotyaev, 1997, syn. nov.; = Z. subgen. Gobicladus Korotyaev, 1997, syn. nov.; = Z. subgen. Scythocladus Korotyaev, 1997, syn. nov.). New placements are: Amalini Wagner, 1936 as a tribe from synonymy under Ceutorhynchini; Acentrotypus Alonso-Zarazaga, 1990, Aizobius Alonso-Zarazaga, 1990, Aspidapion Schilsky, 1901, Catapion Schilsky, 1906, Ceratapion Schilsky, 1901, Cistapion Wagner, 1924,Cyanapion Bokor, 1923, Diplapion Reitter, 1916, Eutrichapion Reitter, 1916, Exapion Bedel, 1887, Helianthemapion Wagner, 1930, Hemitrichapion Voss, 1959, Holotrichapion Györffy, 1956, Ischnopterapion Bokor, 1923, Ixapion Roudier & Tempère,1973, Kalcapion Schilsky, 1906, Lepidapion Schilsky, 1906, Melanapion Wagner, 1930, Mesotrichapion Györffy, 1956, Metapion Schilsky, 1906, Omphalapion Schilsky, 1901, Onychapion Schilsky, 1901, Oryxolaemus AlonsoZarazaga, 1990, Osellaeus Alonso-Zarazaga, 1990, Perapion Wagner, 1907, Phrissotrichum Schilsky, 1901, Pirapion Reitter, 1916, Protapion Schilsky, 1908, Pseudapion Schilsky, Pseudoperapion Wagner, 1930, Pseudoprotapion Ehret, 1990, Pseudostenapion Wagner, 1930, Rhodapion AlonsoZarazaga, 1990, Squamapion Bokor, 1923, Stenopterapion Bokor, 1923, Synapion Schilsky, 1902, Taeniapion Schilsky, 1906, Trichopterapion Wagner, 1930, all as genera from subgenera of Apion Herbst, 1797; Aspidapion subgen. Koestlinia Alonso-Zarazaga, 1990 and Phryssotrichum subgen. Schilskyapion Alonso-Zarazaga, 1990 from synonymy with Apion Herbst, 1797; Phyllobius italicus Solari & Solari, 1903 and Phyllobius reicheidius Desbrochers, 1873, both from subspecies of P. pyri (Linné, 1758); Mogulones aubei (Boheman, 1845) as a valid species from synonymy with M. talbum (Gyllenhal, 1837); Styphlidius italicus Osella, 1981 as species from subspecies of S. corcyreus (Reitter, 1884). Otiorhynchus subgen. Presolanus Pesarini, 2001 is here selected over O. subgen. Pesolanus Pesarini, 2001, alternative original spelling, here rejected. The incorrect original spelling Otiorhynchus nocturnus peetzi Franz, 1938 is emended in O. n. peezi. New combination are: Eremiarhinus (Depresseremiarhinus) dilatatus (Fabricius, 1801), comb. nov.; Eremiarinus (Pseudorhinus) impressicollis (Boheman, 1834) jarrigei (Roudier, 1959); E. (Pseudorhinus) impressicollis luciae (Ragusa, 1883), comb. nov.; E. (Pseudorhinus) impressicollis peninsularis (F. Solari, 1940), comb. nov.; E. (Pseudorhinus) laesirostris (Fairmaire, 1859), comb. nov., all resulting from the new placement of Depresseremiarhinus Pic, 1914 and of Pseudorhinus Melichar, 1923 as subgenera of Eremiarhinus Fairmaire, 1876. The subfamilial name Phytonominae Gistel, 1848 is used as valid over Hyperinae Marseul, 1863. Nomenclatural changes published from 1992 to date, and affecting Italian weevils are also listed.

AbstractIn Sweden, leishmaniasis is an imported disease and its epidemiology and incidence were not known until now. We conducted a retrospective, nationwide, epidemiological study from 1993 to 2016. Probable cases were patients with leishmaniasis diagnoses reported to the Swedish Patient registry, collecting data on admitted patients in Swedish healthcare since 1993 and out-patient visits since 2001. Confirmed cases were those with a laboratory test positive for leishmaniasis during 1993–2016. 299 probable cases and 182 confirmed cases were identified. Annual incidence ranged from 0.023 to 0.35 per 100 000 with a rapid increase in the last 4 years. Of 182 laboratory-verified cases, 96 were diagnosed from 2013 to 2016, and in this group, almost half of the patients were children under 18 years. Patients presented in different healthcare settings in all regions of Sweden. Cutaneous leishmaniasis was the most common clinical manifestation and the majority of infections were acquired in Asia including the Middle East, specifically Syria and Afghanistan. Leishmania tropica was responsible for the majority of cases (42%). A combination of laboratory methods increased the sensitivity of diagnosis among confirmed cases. In 2016, one-tenth of the Swedish population were born in Leishmania-endemic countries and many Swedes travel to these countries for work or vacation. Swedish residents who have spent time in Leishmania-endemic areas, could be at risk of developing disease some time during their lives. Increased awareness and knowledge are needed for correct diagnosis and management of leishmaniasis in Sweden.

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.

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.

Amount of client and also kind of industrial often result a work of audit have character is clerical andonly pursuing goals " Deadline". So that sometimes work of audit become something is routine. Workof audit which in have character the routine and clerical can weaken of supervision. This matterindication height turnover at the accounting firm.This research aim to know influence of supervisory actions to job satisfaction of entry-level staff, eithersimultaneously and also partially at the accounting firm in Bandung City. And for that used by thefollowing grand theory: for the variable of leadership and mentoring to job satisfaction, used theoryfrom Malayu ( 2003:189) and Robbin ( 1993:182). Variable of working conditions to jobsatisfaction, used theory from Luthan ( 1995:122) and Robbin ( 1993:181). While variable ofassignment to job satisfaction, used theory from Luthan ( 1995:121) and Robbin ( 1993:181).This research use the census method, with population counted 60 responder, that is entry-level stafffrom the accounting firm in Bandung City. Data required consisted of primary data obtained throughthe questioner and secondary data supporting this research. To analysis this research used by Analysisof Multiple Regression.The study find that three major element of supervisory actions recommended by the AECC, leadershipand mentoring, working conditions, and assignment, simultaneously have positive influence to jobsatisfaction of entry level staff equal to 47,20 %. Partially, influence element supervisory actions to jobsatisfaction of entry-level staff, leadership and mentoring have positive influence to job satisfaction ofentry-level staff equal to 19,70 %, working conditions have positive influence to job satisfaction equalto 32,50 %, and assignment have positive influence to job satisfaction equal to 15,20 %.

The tribes Goniaderini Lacordaire, 1859 and Lupropini Lesne, 1926 within the tenebrionid subfamily Lagriinae Latreille, 1825 have previously been shown to be non-monophyletic by molecular phylogenetic analyses. The tribes and constituent genera are here reviewed and redefined morphologically. As part of tribal redefinitions, we establish PrateiniNew Tribe with type genus Prateus LeConte, 1862. We reestablish the subtribe Phobeliina Ardoin, 1961 Revised Status, which is transferred from Goniaderini and placed as a subtribe of Lagriini Latreille, 1825 where it is comprised of Phobelius Blanchard, 1842, and Rhosaces Champion, 1889 (previously in Lagriini: Statirina Blanchard, 1845). The fossil tribe Archaeolupropini Nabozhenko, Perkovsky, & Nazarenko, 2023 is transferred from Lagriinae to Tetratomidae: Tetratominae Billberg, 1820. Keys to extant tribes and subtribes of Lagriinae and genera of Goniaderini, Lupropini, and Prateini are provided. Generic and species-level changes from this work are as follows: Prateini is comprised of the following 15 genera: Antennoluprops Schawaller, 2007, Ardoiniellus Schawaller, 2013, Bolitrium Gebien, 1914, Enicmosoma Gebien, 1922, Indenicmosoma Ardoin, 1964, Iscanus Fauvel, 1904, Kuschelus Kaszab, 1982, Lorelopsis Champion, 1896, Mesotretis Bates, 1872, Microcalcar Pic, 1925, Micropedinus Lewis, 1894, Paratenetus Spinola, 1845, Prateus, Terametus Motschulsky, 1869, and Tithassa Pascoe, 1860. Lorelus Sharp, 1876 is Returned to Synonymy with Prateus, resulting in the following 49 New Combinations: Prateus angulatus (Doyen & Poinar, 1994), P. angustulus (Champion, 1913), P. armatus (Montrouzier, 1860), P. biroi (Kaszab, 1956), P. blairi (Kaszab, 1955), P. brevicornis (Champion, 1896), P. breviusculus (Champion, 1913), P. caledonicus (Kaszab, 1982), P. carolinensis (Blair, 1940), P. chinensis (Kaszab, 1940), P. clarkei (Kulzer, 1957), P. crassicornis (Broun, 1880), P. crassepunctatus (Kaszab, 1982), P. cribricollis (Kaszab, 1940), P. curvipes (Champion, 1913), P. dybasi (Kulzer, 1957), P. fijianus (Kaszab, 1982), P. fumatus (Lea, 1929), P. glabriventris (Kaszab, 1982), P. greensladei (Kaszab, 1982), P. guadeloupensis (Kaszab, 1940), P. hirtus (Kaszab, 1982), P. ivoirensis (Ardoin, 1969), P. kanak (Kaszab, 1986), P. kaszabi (Watt, 1992), P. laticornis (Watt, 1992), P. latulus (Broun, 1910), P. longicornis (Kaszab, 1982), P. mareensis (Kaszab, 1982), P. marginalis (Broun, 1910), P. niger (Kaszab, 1982), P. norfolkianus (Kaszab, 1982), P. obtusus (Watt, 1992), P. ocularis (Fauvel, 1904), P. opacus (Watt, 1992), P. palauensis (Kulzer, 1957), P. politus (Watt, 1992), P. priscus (Sharp, 1876), P. prosternalis (Kaszab, 1982), P. pubescens (Broun, 1880), P. pubipennis (Lea, 1929), P. punctatus (Watt, 1992), P. quadricollis (Broun, 1886), P. queenslandicus (Kaszab, 1986), P. rugifrons (Champion, 1913), P. solomonis (Kaszab, 1982), P. tarsalis (Broun, 1910), P. unicornis (Kaszab, 1982), and P. watti (Kaszab, 1982). Microlyprops Kaszab, 1939 is placed as a New Synonym of Micropedinus resulting in the following New Combinations: Micropedinus ceylonicus (Kaszab, 1939) and M. maderi (Kaszab, 1940). LorelopsisRevised Status is revalidated as a genus and eight species formerly in Lorelus are transferred to it resulting in the following six New Combinations: Lorelopsis bicolor (Doyen, 1993), L. glabrata (Doyen, 1993), L. exilis (Champion, 1913), L. foraminosa (Doyen & Poinar, 1994), L. minutulis (Doyen & Poinar, 1994), L. trapezidera (Champion, 1913), and L. wolcotti (Doyen, 1993). Lorelopsis pilosa Champion, 1896 becomes a Restored Combination. In Goniaderini, Aemymone Bates, 1868 Revised Status and Opatresthes Gebien, 1928 Revised Status, which were recently considered as subgenera of Goniadera Perty, 1832, are restored as valid genera based on new character analysis resulting in the following New Combinations: Aemymone hansfranzi (Ferrer & Delatour, 2007), A. simplex (Fairmaire, 1889), A. striatipennis (Pic, 1934) and Restored Combinations: Aemymone cariosa (Bates, 1868), A. crenata Champion, 1893, and A. semirufa Pic, 1917. Gamaxus Bates, 1868 is Returned to Synonymy with Phymatestes Pascoe, 1866, and the type species Gamaxus hauxwelli Bates, 1868 is placed as a New Synonym of Phymatestes brevicornis (Lacordaire, 1859). The following seven genera are placed as New Synonyms of Anaedus Blanchard, 1842: Microanaedus Pic, 1923, Pengaleganus Pic, 1917, Pseudanaedus Gebien, 1921, Pseudolyprops Fairmaire, 1882, Spinolyprops Pic, 1917, Spinadaenus Pic, 1921, and Sphingocorse Gebien, 1921. Fourteen species described by Pic in Aspisoma Duponchel & Chevrolat, 1841 (not Aspisoma Laporte, 1833) are returned to Tenebrionidae as valid species of Anaedus. These synonymies necessitate the following 51 New Combinations: Anaedus albipes (Gebien, 1921), A. amboinensis (Kaszab, 1964), A. amplicollis (Fairmaire, 1896), A. anaedoides (Gebien, 1921), A. angulicollis (Gebien, 1921), A. angustatus (Pic, 1921), A. australiae (Carter, 1930), A. bartolozzii (Ferrer, 2002), A. beloni Fairmaire, 1888), A. biangulatus (Gebien, 1921), A. borneensis (Pic, 1917), A. carinicollis (Gebien, 1921), A. conradti (Gebien, 1921), A. cribricollis (Schawaller, 2012), A. gabonicus (Pic, 1917), A. himalayicus (Kaszab, 1965), A. inaequalis (Pic, 1917), A. jacobsoni (Gebien, 1927), A. lateralis (Pic, 1917), A. latus (Pic, 1917), A. longeplicatus (Gebien, 1921) , A. maculipennis (Schawaller, 2011), A. major (Pic, 1917), A. nepalicus (Kaszab, 1975), A. nigrita (Gebien, 1927), A. notatus (Pic, 1923), A. pakistanicus (Schawaller, 1996), A. pinguis (Gebien, 1927), A. punctatus (Carter, 1914), A. raffrayi (Pic, 1917), A. rufithorax (Pic, 1917), A. rufus (Pic, 1917), A. serrimargo (Gebien, 1914), A. sumatrensis (Pic, 1917), A. terminatus (Gebien, 1921), A. testaceicornis (Pic, 1921), A. testaceipes (Pic, 1917), A. thailandicus (Schawaller, 2012), A. trautneri (Schawaller, 1994); and 13 restored combinations: Anaedus boliviensis (Pic, 1934), A. claveri (Pic, 1917), A. diversicollis (Pic, 1917), A. elongatus (Pic, 1934), A. guyanensis (Pic, 1917), A. holtzi (Pic, 1934), A. inangulatus (Pic, 1934), A. inhumeralis (Pic, 1917), A. mendesensis (Pic, 1917), A. minutus (Pic, 1917), A. rufimembris (Pic, 1932), A. rufipennis (Pic, 1917), A. subelongatus (Pic, 1932). The new synonymies with Anaedus necessitate the following six New Replacement NamesAnaedus maculipennis (for Spinolyprops maculatus Kulzer, 1954), A. grimmi (for Aspisoma forticornis Pic, 1917), A. minimus (for Anaedus minutus Pic, 1938), A. merkli (for Anaedus diversicollis Pic, 1938), A. ottomerkli (for Anaedus lateralis Pic, 1923), A. schawalleri (for Anaedus nepalicus Schawaller, 1994). Capeluprops Schawaller, 2011 is removed from Lupropini and provisionally placed in Laenini Seidlitz, 1895. Plastica Waterhouse, 1903 is transferred from Apocryphini Lacordaire, 1859 to Laenini. Paralorelopsis Marcuzzi, 1994 is removed from Lupropini and provisionally placed in Lagriinae incertae sedis. Pseudesarcus Champion, 1913 is transferred from Lagriinae incertae sedis to Diaperinae incertae sedis. Falsotithassa Pic, 1934 is transferred from Lupropini to Leiochrinini Lewis, 1894 (Diaperinae). Mimocellus Wasmann, 1904 is transferred from Lupropini to Tenebrionidae incertae sedis, and likely belongs in either Diaperinae or Stenochiinae.

This paper provides a taxonomic review of the titi monkeys, genus Callicebus, and describes two new species from central Brazilian Amazonia, Callicebus bernhardi and Callicebus stephennashi. Previous revisions include Hershkovitz (1988, 1990), Kobayashi (1995), Kobayashi and Langguth (1999) and Groves (1993, 2001). Here we arrange the titi monkeys, genus Callicebus Thomas, 1903, into five Species Groups or clades, and a total of 28 species. The Callicebus donacophilus Group is represented by the following species: Callicebus modestus Lönnberg, 1939, Callicebus donacophilus (d’Orbigny, 1836), Callicebus pallescens Thomas, 1907 (treated by Hershkovitz as a subspecies of C. donacophilus), Callicebus olallae Lönnberg, 1939, and Callicebus oenanthe Thomas, 1924. The Callicebus moloch Group is represented by the following species: Callicebus cinerascens (Spix, 1823), Callicebus hoffmannsi Thomas, 1908, Callicebus baptista Lönnberg, 1939 (treated by Hershkovitz as a subspecies of C. hoffmannsi), Callicebus brunneus (Wagner, 1842), Callicebus moloch (Hoffmannsegg, 1807), and the new species here described as Callicebus bernhardi. The Callicebus cupreus Group is represented by the following species: Callicebus cupreus (Spix, 1823), Callicebus discolor (I. Geoffroy & Deville, 1848) (treated by Hershkovitz as a subspecies of C. cupreus), Callicebus ornatus (Gray, 1866) (treated by Hershkovitz as a subspecies of Callicebus cupreus), Callicebus caligatus (Wagner, 1842), Callicebus dubius Hershkovitz, 1988, and the new species here described as Callicebus stephennashi. The Callicebus torquatus Group is represented by the following species: Callicebus torquatus (Hoffmannsegg, 1807), Callicebus lugens (Humboldt, 1811) (treated by Hershkovitz as a subspecies of C. torquatus), Callicebus purinus Thomas, 1927 (treated by Hershkovitz as a subspecies of C. torquatus), Callicebus lucifer Thomas, 1914 (treated by Hershkovitz as a subspecies of C. torquatus), Callicebus regulus Thomas, 1927 (treated by Hershkovitz as a subspecies of C. torquatus), and Callicebus medemi Hershkovitz, 1963 (treated by Hershkovitz as a subspecies of C. torquatus). The Callicebus personatus Group is treated separately from the Callicebus moloch Group and is represented by the following species: Callicebus personatus (É. Geoffroy, 1812), Callicebus melanochir (Wied-Neuwied, 1820) (treated by Hershkovitz as a subspecies of C. personatus), Callicebus nigrifrons (Spix, 1823) (treated by Hershkovitz as a subspecies of C. personatus), Callicebus barbarabrownae Hershkovitz, 1990 (treated by Hershkovitz as a subspecies of C. personatus), and Callicebus coimbrai Kobayashi & Langguth, 1999. Callicebus bernhardi was discovered in the Rio Aripuanã basin in 1996 by M. G. M. van Roosmalen, who also discovered Callicebus stephennashi in 2001, while traveling on the Rio Purus. The geographic distributions of all hitherto recognized Callicebus species are updated, and the validity of the river barrier hypothesis for titis and other Amazonian primates is discussed, along with their conservation status.

Estudou-se as taxas de morbidade e mortalidade hospitalar por tumores (grupo II da CID) em Ribeirão Preto, nos anos de 1990 a 1993, em pacientes atendidos nos hospitais gerais do município, realizando um levantamento dos dados das folhas de altas hospitalares. Os coeficientes de mortalidade hospitalar (CMH), por tumores malignos (câncer), apresentaram uma discreta variação e sempre maior entre os homens. A mortalidade, referente aos homens, diminuiu de 15,37%, em 1990, para 12,79% em 1993. Quanto à localização, em 1990 e 1991, os tumores dos órgãos respiratórios e intratorácicos apresentaram um CMH pouco acima de 20% e, em 1992 e 1993, a localização mais letal foi a dos órgãos digestivos e peritônio. A mortalidade por câncer entre as mulheres, em 1990, foi de 12,96%, em 1992, 7,61% e, em 1993, 9,22%. Durante o período, observou-se um aumento contínuo na proporção de internações, variando de 5,89%, em 1990, para 7,39% em 1993. Quanto à duração média de internação (DMI), diminuiu de 6,15 dias para 4,62 dias entre os homens e de 4,75 dias para 3,61 dias entre as mulheres. Entre os homens, houve um aumento das internações nas faixas etárias até 69 anos, subindo de 74,5% em 1990, para 85,5% em 1993. As neoplasias mais freqüentes foram as de traquéia, brônquios e pulmões (CID-162) em primeiro (10%), em seguida as de estômago (CID-151), que diminuíram de 9 para 6%. Para as mulheres, não houve alterações nas faixas etárias no decorrer do estudo e o maior número de casos ocorreu na faixa de 40 a 59 anos (40%). Quanto às Neoplasias mais freqüentes foram o câncer de mama (CID-174) com 11% (bem mais alto do que para as demais), em seguida as Neoplasias de colo de útero (CID-180), de ovário e anexos (CID-183) e leucemia mielóide (CID-205).

To investigate the abundance and distribution of small mammals relative to edge in a fragmented prairie landscape, small mammals were trapped in south-central Saskatchewan from 1991 to 1993 in four different habitat types: idle pasture, delayed hay, dense nesting cover, and rights-of-way. In total, 995 small mammals, representing nine species, were captured on 14 182 trap-nights. No edge effect was recorded in idle pasture or dense nesting cover; however, an edge effect was observed in delayed hay fields. Edge effect across all habitats was dependent on season: relative abundance of small mammals was significantly higher along edges in spring but not in summer. Of the two most common species captured, Peromyscus maniculatus showed no affinity for edges, while Microtus pennsylvanicus was significantly more abundant along edges than in the habitat interior. Relative abundance of small mammals was highest in dense nesting cover, intermediate in delayed hay and along rights-of-way, and lowest in idle pasture. Relative abundance was also lower in spring than in summer. Species richness was higher along edges than in the habitat interior and was also greater in summer than in spring. Species diversity showed no edge or season effect.

Introductions of the rabbit flea, Spilopsyllus cuniculi (Dale), were made on an island (3.1 km2) of the Kerguelen subantarctic archipelago in January and December 1987. Despite a small founding population, the species succeeded in establishing itself. Three years after introduction, the rate of spread was 614 ± 133 m (between 1990 and 1993). Despite the subantarctic climate of Kerguelen, the burdens were similar to those noted in habitats favourable to this ectoparasite. The flea burden of adult rabbits after colonisation of the whole island was higher for pregnant females (182 ± 21, n = 98) than for non-pregnant ones (85 ± 16, n = 68) or males (20 ± 3, n = 116). The circulation of myxoma virus, present on this island for several decades, has been favoured by the flea. As a result, the proportion of rabbits with antibodies rose from 34% before introduction of the flea to 85% in 1998. Moreover, the introduction of fleas has changed the relative proportions of both adult males and females with antibodies. Those proportions were not different before the introduction but more males than females showed antibodies when the flea colonised the whole island. Finally, the prospects of the introduction of Spilopsyllus cuniculi on the main island of the archipelago are discussed.

A list of available taxonomic names in Curculionidae: Scolytinae and Platypodinae in familyand genus-groups is given, together with some remarks on unavailable nominal taxa. Comments are provided on their status and nomenclature, and additions and corrections to extant catalogues given, as a first step for their inclusion in the electronic catalogue ‘WTaxa’. Available names, not recognised as such in current published catalogues, are: Mecopelminae Thompson, 1992; Trypodendrina Nunberg, 1954; Archaeoscolytus Butovitsch, 1929; Camptocerus Dejean, 1821; Coccotrypes Eichhoff, 1878 (April); Coptogaster Illiger, 1804; Cosmoderes Eichhoff, 1878 (April); Cryptoxyleborus Wood & Bright, 1992; Cylindra Illiger, 1802; Dendrochilus Schedl, 1963; Dendrocranulus Schedl, 1938; Doliopygus Browne, 1962; Doliopygus Schedl, 1972; Erioschidias Wood, 1960; Ernopocerus Wood, 1954; Idophelus Rye, 1877; Lepicerus Eichhoff, 1878 (April); Lepidocerus Rye, 1880; Miocryphalus Schedl, 1963; Ozopemon Hagedorn, 1910; Phloeoditica Schedl, 1963; Pinetoscolytus Butovitsch, 1929; Pycnarthrum Eichhoff, 1878 (April); Pygmaeoscolytus Butovitsch, 1929; Scolytogenes Eichhoff, 1878 (April); Spinuloscolytus Butovitsch, 1929; Stephanopodius Schedl, 1963; Stylotentus Schedl, 1963; Thamnophthorus Blackman, 1942; Trachyostus Browne, 1962; Treptoplatypus Schedl, 1972; Triarmocerus Eichhoff, 1878 (April); Trypodendrum Agassiz, 1846; Tubuloscolytus Butovitsch, 1929; Xelyborus Schedl, 1939. Unavailable names, not recognised as such in the current published catalogues, are: Chaetophloeini Schedl, 1966; Eidophelinae Murayama, 1954; Mecopelmini Wood, 1966; Strombophorini Schedl, 1960; Tomicidae Shuckard, 1840; Trypodendrinae Trédl, 1907; Acryphalus Tsai & Li, 1963; Adryocoetes Schedl, 1952; Asetus Nunberg, 1958; Carphoborites Schedl, 1947; Charphoborites Schedl, 1947; Cryptoxyleborus Schedl, 1937; Cylindrotomicus Eggers, 1936; Damicerus Dejean, 1835; Damicerus Dejean, 1836; Dendrochilus Schedl, 1957; Dendrocranulus Schedl, 1937; Doliopygus Schedl, 1939; Erioschidias Schedl, 1938; Ernopocerus Balachowsky, 1949; Gnathotrichoides Blackman, 1931; Ipites Karpiński, 1962; Isophthorus Schedl, 1938; Jugocryphalus Tsai & Li, 1963; Landolphianus Schedl, 1950; Mesopygus Nunberg, 1966; Micraciops Schedl, 1953; Miocryphalus Schedl, 1939; Mixopygus Nunberg, 1966; Neohyorrhynchus Schedl, 1962; Neophloeotribus Eggers, 1943; Neopityophthorus Schedl, 1938; Neoxyleborus Wood, 1982; Phloeoditica Schedl, 1962; Platypinus Schedl, 1939; Platyscapulus Schedl, 1957; Platyscapus Schedl, 1939; Pygodolius Nunberg, 1966; Scutopygus Nunberg, 1966; Stephanopodius Schedl, 1941; Stylotentus Schedl, 1939; Taphrostenoxis Schedl, 1965; Tesseroplatypus Schedl, 1935; Thamnophthorus Schedl, 1938; Thylurcos Schedl, 1939; Trachyostus Schedl, 1939; Treptoplatus Schedl, 1939. The name Tesseroceri Blandford, 1896, incorrectly given as “Tesserocerini genuini” in current catalogues, is unavailable as basionym for the family-group name, since it was proposed as a genusgroup name. Resurrected names from synonymy are: Hexacolini Eichhoff, 1878 from synonymy under Ctenophorini Chapuis, 1869 (invalid name because its type genus is a homonym) and given precedence over Problechilidae Eichhoff, 1878 under Art. 24.2; Hylurgini Gistel, 1848 from virtual synonymy under Tomicini C.G. Thomson, 1859 (unavailable name); Afromicracis Schedl, 1959 from synonymy under Miocryphalus Schedl, 1939 (an unavailable name) to valid genus; Costaroplatus Nunberg, 1963 from synonymy under Platyscapulus Schedl, 1957 (an unavailable name) to valid genus; Cumatotomicus Ferrari, 1867 from synonymy under Ips DeGeer, 1775 to valid subgenus of the same; Hapalogenius Hagedorn, 1912 from synonymy under Rhopalopselion Hagedorn, 1909 to valid genus; Pseudips Cognato, 2000, from synonymy under Orthotomicus Ferrari, 1867 to valid genus. New synonyms are: Hexacolini Eichhoff, 1878 (= Erineophilides Hopkins, 1920, syn. nov.); Hypoborini Nuesslin, 1911 (= Chaetophloeini Schedl, 1966, unavailable name, syn. nov.); Scolytini Latreille, 1804 (= Minulini Reitter, 1913, syn. nov.); Afromicracis Schedl, 1959 (= Miocryphalus Schedl, 1963, syn. nov.); Aphanarthrum Wollaston, 1854 (= Coleobothrus Enderlein, 1929, syn. nov.); Coccotrypes Eichhoff, 1878 (April) (= Coccotrypes Eichhoff, 1878 (December), syn. nov.); Cosmoderes Eichhoff, 1878 (April) (= Cosmoderes Eichhoff, 1878 (December), syn. nov.); Cumatotomicus Ferrari, 1867 (=Emarips Cognato, 2001, syn. nov.); Doliopygus Browne, 1962 (=Doliopygus Schedl, 1972, syn. nov.); Eidophelus Eichhoff, 1875 (= Idophelus Rye, 1877, syn. nov.); Hapalogenius Hagedorn, 1912 (= Hylesinopsis Eggers, 1920, syn. nov.); Phloeoborus Erichson, 1836 (= Phloeotrypes Agassiz, 1846, syn. nov.); Pycnarthrum Eichhoff, 1878 (April) (= Pycnarthrum Eichhoff, 1878 (December), syn. nov.); Scolytogenes Eichhoff, 1878 (April) (= Scolytogenes Eichhoff, 1878 (December) = Lepicerus Eichhoff, 1878 (December) = Lepidocerus Rye, 1880, synn. nov.); Trypodendron Stephens, 1830 (=Xylotrophus Gistel, 1848 = Trypodendrum Gistel, 1856, synn. nov.); Xylechinus Chapuis, 1869 (= Chilodendron Schedl, 1953, syn. nov.); Cosmoderes monilicollis Eichhoff, 1878 (April) (= Cosmoderes monilicollis Eichhoff, 1878 (December), syn. nov.); Hylastes pumilus Mannerheim, 1843 (= Dolurgus pumilus Eichhoff, 1868, syn. nov.); Hypoborus hispidus Ferrari, 1867 (= Pycnarthrum gracile Eichhoff, 1878 (April) syn. nov.); Miocryphalus agnatus Schedl, 1939 (= Miocryphalus agnatus Schedl, 1942, syn. nov.); Miocryphalus congonus Schedl, 1939 (= Miocryphalus congonus Eggers, 1940, syn. nov.); Lepicerus aspericollis Eichhoff, 1878 (April) = Lepicerus aspericollis Eichhoff, 1878 (December), syn. nov.); Spathicranuloides moikui Schedl, 1972 (June) (= Spathicranuloides moikui Schedl, 1972 (December), syn. nov.); Triarmocerus cryphalo-ides Eichhoff, 1878 (April) (= Triarmocerus cryphaloides Eichhoff, 1878 (December), syn. nov.); Scolytogenes darvini Eichhoff, 1878 (April) (= Scolytogenes darwinii Eichhoff, 1878 (December), syn. nov.). New type species designations are: Bostrichus dactyliperda Fabricius, 1801 for Coccotrypes Eichhoff, 1878 (April); Triarmocerus cryphaloides Eichhoff, 1878 (April) for Triarmocerus Eichhoff, 1878 (April); Ozopemon regius Hagedorn, 1908 for Ozopemon Hagedorn, 1910 (non 1908); Dermestes typographus Linnaeus, 1758 for Bostrichus Fabricius, 1775 (non Geoffroy, 1762). New combinations are: Afromicracis agnata (Schedl, 1939), A. attenuata (Eggers, 1935), A. ciliatipennis (Schedl, 1979), A. congona (Schedl, 1939), A. dubia (Schedl, 1950), A. elongata (Schedl, 1965), A. grobleri (Schedl, 1961), A. klainedoxae (Schedl, 1957), A. longa (Nunberg, 1964), A. natalensis (Eggers, 1936), A. nigrina (Schedl, 1957), A. nitida (Schedl, 1965), A. pennata (Schedl, 1953) and A. punctipennis (Schedl, 1965) all from Miocryphalus; Costaroplatus abditulus (Wood, 1966), C. abditus (Schedl, 1936), C. carinulatus (Chapuis, 1865), C. clunalis (Wood, 1966), C. cluniculus (Wood, 1966), C. clunis (Wood, 1966), C. costellatus (Schedl, 1933), C. frontalis (Blandford, 1896), C. imitatrix (Schedl, 1972), C. manus (Schedl, 1936), C. occipitis (Wood, 1966), C. pulchellus (Chapuis, 1865), C. pulcher (Chapuis, 1865), C. pusillimus (Chapuis, 1865), C. subabditus (Schedl, 1935), C. turgifrons (Schedl, 1935) and C. umbrosus (Schedl, 1936) all from Platyscapulus; Hapalogenius africanus (Eggers, 1933), H. alluaudi (Lepesme, 1942), H. angolanus (Wood, 1988), H. angolensis (Schedl, 1959), H. arabiae (Schedl, 1975), H. atakorae (Schedl, 1951), H. ater (Nunberg, 1967), H. baphiae (Schedl, 1954), H. brincki (Schedl, 1957), H. confusus (Eggers, 1935), H. decellei (Nunberg, 1969), H. dimorphus (Schedl, 1937), H. dubius (Eggers, 1920), H. emarginatus (Nunberg, 1973), H. endroedyi (Schedl, 1967), H. fasciatus (Hagedorn, 1909), H. ficus (Schedl, 1954), H. fuscipennis (Chapuis, 1869), H. granulatus (Lepesme, 1942), H. hirsutus (Schedl, 1957), H. hispidus (Eggers, 1924), H. horridus (Eggers, 1924), H. joveri (Schedl, 1950), H. kenyae (Wood, 1986), H. oblongus (Eggers, 1935), H. orientalis (Eggers, 1943), H. pauliani (Lepesme, 1942), H. punctatus (Eggers, 1932), H. quadrituberculatus (Schedl, 1957), H. rhodesianus (Eggers, 1933), H. saudiarabiae (Schedl, 1971), H. seriatus (Eggers, 1940), H. squamosus (Eggers, 1936), H. striatus (Schedl, 1957), H. sulcatus Eggers, 1944), H. togonus (Eggers, 1919), H. ugandae (Wood, 1986) and H. variegatus (Eggers, 1936), all from Hylesinopsis. New ranks are: Diapodina Strohmeyer, 1914, downgraded from tribe of Tesserocerinae to subtribe of Tesserocerini; Tesserocerina Strohmeyer, 1914, downgraded from tribe of Tesserocerinae to subtribe of Tesserocerini. New placements are: Coptonotini Chapuis, 1869 from tribe of Coptonotinae to tribe of Scolytinae; Mecopelmini Thompson, 1992, from tribe of Coptonotinae to tribe of Platypodinae; Schedlariini Wood & Bright, 1992, from tribe of Coptonotinae to tribe of Platypodinae; Spathicranuloides Schedl, 1972, from Platypodinae s.l. to Tesserocerina; Toxophthorus Wood, 1962 from Scolytinae incertae sedis to Dryocoetini. Confirmed placements are: Onychiini Chapuis, 1869 to tribe of Cossoninae (including single genus Onychius Chapuis, 1869); Sciatrophus Sampson, 1914 in Cossoninae incertae sedis; Cryphalites Cockerell, 1917 in Zopheridae Colydiinae. Corrected spellings are: Micracidini LeConte, 1876 for Micracini; Phrixosomatini Wood, 1978 for Phrixosomini. Gender agreements are corrected for species of several genera.

The publication contains review of the genera of jumping spiders: Emertonius, Evarcha, Nigorella, Padilothorax, Stagetillus, and delimits five more new genera, provides graphic documentation for species considered recognizable and adds description of four new species. The taxonomic procedures are carried out according to methodology of "pragmatic classification", which stresses importance of graphic diagnostic characters presented in a comparative way (see also review at “Methodological postulates” subchapter). Some new procedures are introduced, testing their acceptability.The following new genera are delimited and described in this paper: Evarcha Simon, 1889 s. s. (a part of Evarcha s. l.), Evacin Prószyński, 2017 gen. n., Evalba Prószyński, 2017 gen. n., Evaneg Prószyński, 2017 gen. n., Evawes Prószyński, 2017 gen. n., Padillothorus gen. n. Genus Emertonius Peckham & Peckham, 1892, misinterpreted twice by the WSC Editors, is reinstated again, with full diagnostic documentation repeated.The following new species are described in this paper - Emertonius koomeni sp. n., Evacin besar sp. n., Evaneg aegiptiaca Prószyński, 2017 sp. n ."Emertonius" palawanensis sp. n.New synonyms documented.Evarcha acuta Wesolowska, 2006 = Evacin acuta (Wesolowska, 2006), comb. n., Evarcha bulbosa Zabka, 1985 = Evacin bulbosa (Zabka, 1985), comb. n., Evarcha cancellata Simon, 1902 = Evacin cancellata (Simon, 1902), comb. n., Evarcha flagellaris Haddad & Wesolowska, 2011= Evacin flagellaris (Haddad & Wesolowska, 2011), Evarcha flavocincta (C. L. Koch, 1846) = Evacin flavocincta (C. L. Koch, 1846) comb. n., Evarcha heteropogon Simon, 1903 = Evacin heteropogon Simon, 1903, comb. n., Evarcha infrastriata (Keyserling, 1881) = Evacin infrastriata (Keyserling, 1881), comb. n., Evarcha karas Wesolowska, 2011 = Evarcha karas (Wesolowska, 2011), comb. n., Evarcha kirghisica Rakov, 1997 = Evacin kirghisica (Rakov, 1997), comb. n., Evarcha kochi Simon, 1902 = Evacin kochi Simon, 1902 comb. n., Evarcha nigrifrons (Koch C.L., 1846) = Evacin nigrifrons (Koch C.L., 1846), comb. n., Evarcha optabilis Fox, 1937 = Evacin optabilis (Fox, 1937), comb. n., Evarcha pococki Zabka, 1985 = Evacin pococki (Zabka 1985), comb. n., Evarcha pulchella Thorell, 1895 = Evacin pulchella (Thorell, 1895), comb. n., Evarcha pseudopococki Peng X., Xie L. & Kim, 1993 = Evacin pseudopococki (Peng X., Xie L. & Kim, 1993), comb. n., Evarcha reiskindi Berry, Beatty, Proszynski, 1996 = Evacin reiskindi (Berry, Beatty, Proszynski, 1996), comb. n., Evarcha simoni[s] (Thorell, 1892)= Evacin simonis (Thorell, 1892), comb. n., Evarcha striolata Wesołowska & Haddad, 2009 = Evacin striolata (Wesołowska & Haddad, 2009), comb. n., Evarcha vitosa Próchniewicz, 1989 = Evacin vitosa (Próchniewicz, 1989), comb. n.Evarcha albaria (L. Koch, 1878) = Evalba albaria (L. Koch, 1878), comb. n., Evarcha coreana Seo, 1988 = Evalba coreana (Seo, 1988), comb. n., Evarcha fasciata Seo, 1992 = Evalba fasciata (Seo, 1988), comb. n., Evarcha paralbaria Song & Chai, 1992 = Evalba paralbaria (Song & Chai, 1992), comb. n., Evarcha selenaria Suguro & Yahata, 2012 = Evalba selenaria (Suguro & Yahata, 2012), comb. n., Evarcha wulingensis Peng, Xie & Kim, 1993 = Evalba wulingensis (Peng, Xie & Kim, 1993), comb. n.Evarcha armeniaca (Logunov, 1999) = Evaneg armeniaca (Logunov, 1999), comb. n., Evarcha darinurica Logunov, 2001 = Evaneg darinurica (Logunov, 2001) , comb. n., Evarcha negevensis (Proszynski, 2000) = Evaneg negevensis (Proszynski, 2000) comb. n., Evarcha nenilini Rakov, 1997= Evaneg nenilini (Rakov, 1997), comb. n., Evarcha nepos ( O. Pickard-Cambridge, 1872) = Evaneg nepos (O. Pickard-Cambridge, 1872), comb. n., Evarcha nigricans Dalmas, 1920 = Evaneg nigricans (Dalmas, 1920), comb. n.,Evarcha pileckii Proszynski, 2000 = Evaneg pileckii (Proszynski, 2000), comb. n., Evarcha praeclara Prószyński & Wesolowska, in Prószyński, 2003 = Evaneg praeclara (Prószyński & Wesolowska, in Prószyński, 2003), comb. n., Evarcha seyun Wesolowska W., van Harten, 2007 = Evaneg seyun (Wesolowska W., van Harten, 2007), comb. n., Neaetha aegyptiaca Denis, 1947 female only = Evaneg aegyptiaca (Prószyński, 2017) ), comb. n., Neaetha aegyptiaca Denis, 1947 male only = Hyllus aegyptiacus (Denis, 1947), comb. n.Evarcha arabica Wesolowska & van Harten, 2007 = Evawes arabica (Wesolowska & van Harten, 2007) comb. n., Evarcha awashi Wesolowska & Tomasiewicz, 2008 = Evawes awashi (Wesolowska & Tomasiewicz, 2008) comb. n., Evarcha bakorensis Wesolowska & Russel-Smith 2011 = Evawes bakorensis (Wesolowska, Russel-Smith 2011) comb.n., Evarcha bicuspidata Peng & Li, 2003 = Evawes bicuspidata (Peng & Li, 2003) comb. n., Evarcha bihastata Wesolowska & Russell-Smith, 2000 = Evawes bihastata (Wesolowska & Russell-Smith, 2000), comb.n., Evarcha carbonaria (Lessert, 1927) = Evawes carbonaria (Lessert, 1927), comb.n., Evarcha chubbi Lessert, 1925 = Evawes chubbi (Lessert, 1925), comb. n., Evarcha culicivora Wesolowska & Jackson 2003 = Evawes culicivora (Wesolowska & Jackson 2003) comb. n., Evarcha denticulata Wesołowska & Haddad, 2013 = Evawes denticulata (Wesołowska & Haddad, 2013), comb.n., Evarcha elegans Wesolowska & Russel-Smith, 2000 = Evawes elegans (Wesolowska & Russel-Smith, 2000), comb. n., Evarcha ignea Wesołowska & Cumming 2008= Evawes ignea (Wesołowska & Cumming 2008), comb. n., Evarcha jucunda (Lucas, 1846) = Evawes jucunda (Lucas, 1846) comb. n., Evarcha longula (Thorell, 1881) = Evawes longula (Thorell, 1881) comb. n., Evarcha maculata Rollard & Wesolowska, 2002 = Evawes maculata (Rollard & Wesolowska, 2002), comb. n., Evarcha madagascariensis Proszynski, 1992 = Evawes madagascariensis (Proszynski, 1992), comb. n., Evarcha mirabilis Wesołowska & Haddad 2009 = Evawes mirabilis (Wesołowska & Haddad 2009), comb.n., Evarcha patagiata (O. Pickard-Cambridge, 1872) = Evawes patagiata (O. Pickard-Cambridge, 1872), comb.n., Evarcha picta Wesolowska & van Harten, 2007 = Evawes picta (Wesolowska & van Harten, 2007), comb. n., Evarcha pinguis Wesołowska & Tomasiewicz, 2008 = Evawes pinguis (Wesołowska, Tomasiewicz, 2008), comb. n., Evarcha prosimilis Wesolowska & Cumming, 2008= Evawes prosimilis (Wesolowska & Cumming, 2008), comb. n., Evarcha zimbabwensis Wesolowska & Cumming, 2008 = Evawes zimbabwensis (Wesolowska & Cumming, 2008), comb. n.Evarcha hirticeps (Song & Chai, 1992) = Nigorella hirticeps (Song & Chai, 1992), comb. n., Evarcha hunanensis Peng, Xie & Kim, 1993 - withdrawal from synonymy = Nigorella hunanensis (Peng, Xie & Kim, 1993), comb. n., Evarcha petrae Prószyński, 1992 = Nigorella petrae (Prószyński, 1992), comb. n., Evarcha sichuanensis Peng, Xie & Kim, 1993 = Nigorella sichuanensis (Peng, Xie & Kim, 1993), comb. n.Hyllus fischeri Bösenberg & Strand, 1906 = Evacin fischeri (Bösenberg & Strand, 1906), comb. n. (separated from synonymy of Evarcha flavocincta).Hasarius simonis Thorell, 1892 = Evacin simonis (Thorell, 1892), comb. n. (separated from synonymy of Evarcha flavocincta).Myrmarachne aureonigra Edmunds, Prószyński, 2003) = Myrmaplata aureonigra (Edmunds, Prószyński, 2003), comb. n.Myrmarachne exasperans (Peckham & Peckham, 1892) = Emertonius exasperans Peckham & Peckham, 1892 (return to original combination),"Myrmarachne" "exasperans": Wanless 1978: 235, f. 1A-F, not f. 2) (male from Palawan only) = "Emertonius" palawanensis sp. n.,Myrmarachne grossa Edmunds & Prószyński, 2003 = Toxeus grossus (Edmunds & Prószyński, 2003) comb. n.Neaetha aegyptiaca Denis, 1947 (in part - female) = Evaneg aegiptiaca Prószyński, 2017, sp. n., Neaetha aegyptiaca Denis, 1947 (in part - male) = Hyllus aegiptiacus (Denis, 1947) comb. n.Stagetillus elegans (Reimoser, 1927) = Padillothorus elegans Reimoser, 1927, comb. n., reinstated original combination, Stagetillus semiostrinus (Simon, 1901) = Padillothorax semiostrinus Simon, 1901, comb. n., reinstated original combination, Stagetillus taprobanicus (Simon, 1902) = Padillothorax taprobanicus Simon, 1902, comb. n., reinstated original combination.Viciria alba Peckham & Peckham, 1903 = Evacin alba (Peckham & Peckham, 1903), comb. n.Correction of the following synonyms (rejecting biologically misleading changes by the WSC) documented in this paper. Colyttus kerinci (Prószyński & Deeleman-Reinhold, 2012) = Donoessus kerinci Prószyński & Deeleman-Reinhold, 2012 (returned to the previous combination), Colyttus nigriceps (Simon, 1899) = Donoessus nigriceps (Simon, 1899) (returned to the previous combination), Colyttus striatus (Simon, 1902) = Donoessus striatus Simon, 1902 (returned to the previous combination),Coryphasia heros (Bryant, 1943) = Dinattus heros Bryant, 1943 (returned to the previous combination), Jollas armatus (Bryant, 1943) = "Oningis" armatus Bryant, 1943 (returned to the previous combination), Jollas crassus (Bryant, 1943) = "Oningis" crassus Bryant, 1943 (returned to the previous combination), Laufeia daiqini (Prószyński & Deeleman-Reinhold, 2012) = Junxattus daiqini Prószyński & Deeleman-Reinhold, 2012 (returned to the previous combination), Laufeia eucola (Thorell, 1890) = Orcevia eucola Thorell, 1890 (returned to the previous combination), Laufeia keyserlingi (Thorell, 1890) = Orcevia keyserlingi Thorell, 1890 (returned to the previous combination), Laufeia kuloni (Prószyński & Deeleman-Reinhold, 2012) = Orcevia kuloni Prószyński & Deeleman-Reinhold, 2012, (returned to the previous combination,), Laufeia minuta (Prószyński, 1992) = Lechia minuta (Prószyński, 1992) (returned to the previous combination), Laufeia proszynskii Song, Gu & Chen, 1988= Orcevia proszynskii (Song, Gu & Chen, 1988) (returned to the previous combination), Laufeia squamata = Lechia squamata (returned to the previous combination)Notice on pending revisions Evaneg praeclara (Prószyński & Wesolowska in Prószyński, 2003) (= "Evarcha praeclara") is a composite species, pending taxonomic revision, "Myrmarachne" kilifi Wanless, 1978 - placement and diagnostic characters pending revision, "Myrmarachne" laurentina Bacelar, 1953 - placement and diagnostic characters pending revision.Removal from Evarcha: Evarcha wenxianensis Tang & Yang, 1995 = Yaginumaella wenxianensis (Tang & Yang, 1995) (Fig, 15R).

Field investigations were carried out to estimate water budgeting for the allied components like cropping, poultry, pigeon, fish and mushroom linked in lowland integrated farming systems at Tamil Nadu Agricultural University, Coimbatore during 1993-96. Water requirement for the allied components was estimated by adopting standard methodology. Results revealed that cultivation of rice-greengram-maize and rice-sunnhemp-maize cropping systems each in 0.50 hectare consumed 182 ha cm of water totally in a year. Whereas 201 ha cm of water was needed for rice-soybean-sunflower and rice-gingelly-maize cropping systems in 0.45 ha each involved in integrated farming systems. Poultry, pigeon, fish and mushroom components utilized 0.02, 0.04, 15.84 and 1.37 ha cm of water for their production in a year. Integration of cropping with pigeon + fish mushroom utilized 218 ha cm as against 182 ha em of water with conventional cropping system alone. Integration of poultry and pigeon required very little quantity of water and total water requirement in integration of improved cropping with fish mushroom + poultry/pigeon was lesser than the water requirement of cropping alone in one hectare land area. Integrating efficient allied components with cropping results in effective water budgeting with better economic returns in lowland farming.

Upon its adoption in 1992, the Convention on Biological Diversity (CBD) was greeted with enthusiasm by the conservation community including bird conservationists. Nine years after its entry into force in 1993, the CBD still has to live up to the original high expectations if it is to halt, or even slow, the loss of biodiversity at the ecosystem, species and genetic level. Among the reasons for this shortcoming, the rather vague nature of obligations for the 182 governments who have ratified the Convention is probably the most important. National Biodiversity Strategies and Action Plans (NBSAPs) form the most significant instrument for the implementation of the CBD. The Global Environment Facility (GEF) is supporting the NBSAPs financially, as well as local, national and regional projects, many of which are relevant for bird conservation. Being the best-researched animal taxa, birds could serve relatively easily as indicators for the success of efforts under the Convention. Some cases, where ornithological data are being used within NBSAPs and related processes, are highlighted. From the early stages of planning, bird surveyors should take the potential use of their results by decision-makers into account. For ensuring that survey data are fed into NBSAPs and other similar policy documents, a strong collaboration of ornithologists and birdwatchers with non-governmental conservation organizations is recommended.

7 Background: The European Randomized Study of Screening for Prostate Cancer (ERSPC) applies a prostate- specific antigen (PSA) cut-off >3.0 ng/mL as an indication for biopsy. We analyzed the incidence and disease-specific mortality for prostate cancer (PC) within ERSPC Rotterdam for men with an initial PSA <3.0 ng/ml in a 15-year follow-up period. Methods: From 1993-1999, a total of 42,376 men identified from population registries in the Rotterdam region (55-74 yrs) were randomized to a screening or control arm. During the first screening round 19,950 men were screened, with biopsies being initially recommended in case of abnormal DRE or PSA >4.0 ng/mL. From 1997 on, solely PSA >3.0 ng/mL was used. The screening interval was 4 yrs. A total of 15,758 men (79%) had an initial PSA <3.0 ng/mL. Follow-up was complete until January 2009. Results: From 1993-2008, 915 PC cases were diagnosed in 15,758 men (5.8%, median age 62.3 yrs) with an initial PSA <3.0 ng/mL (733 screen detected and 182 interval detected). Median follow-up was 11 yrs. PC incidence increased significantly with higher initial PSA levels (Table). Aggressive PC (clinical stage >T2c, Gleason score >8, PSA >20 ng/mL, positive lymph nodes or metastases at diagnosis) was detected in 65/733 screen detected PC (8.9%) and 102/182 interval detected PC (56.0%). PC death occurred in 23 cases (5 screen detected and 18 interval detected) in the total population (0.15%), with increasing risk in men with higher initial PSA values. Conclusions: The risk of (aggressive) PC and PC mortality in a screening population with initial PSA <3.0 ng/mL increases significantly with higher PSA levels. The risk of dying of PC is minor in men with initial PSA <1.0 ng/mL. Interval detected PC is more aggressive and has a substantial influence on PC specific mortality. [Table: see text] [Table: see text]

Based on the results of the study of literary and archival primary sources, the paper clarifies the available information about catastrophic and destructive earthquakes in Azerbaijan for the historical period with a magnitude of M≥6. Among the strong historical earthquakes in Azerbaijan there are the following: earthquakes in 427, the Ganja (Goygol in 1139), the Ganja in 1235, the East Caucasian in 1667 (± 1 year), the Mashtaga (1842), numerous Shamakhi earthquakes (1192, 1667, 1668, 1669, 1828, 1859, 1868, 1872, 1902), Ardebil (1924), Lankaran (1913), Caspian earthquakes (957, 1812, 1842, 1852, 1911, 1935, 1961, 1963, 1986, 1989, 2000), which caused both changes in the relief of the Earth’s surface, and the destruction of buildings and numerous human casualties. The background seismicity was investigated based on the results of continuous instrumental observations for the period 1902—2019. Seismic processes are unevenly distributed on the territory of Azerbaijan. Existing catalogs of seismic events have been investigated. The behavioral changes in seismicity parameters have been studied. An overview conceptual analysis of two main methods for assessing seismic hazard is given: probabilistic and deterministic, which have found their wide application in recent decades. In conclusion, the most important and general tasks of future seismological studies are emphasized, which are to be performed in the next decades.

The subtribe Deronectina Galewski, 1994 (Dytiscidae, Hydroporinae, Hydroporini) is distributed in the Nearctic, in the north of the Neotropical region, and in the Palaearctic and Afrotropical regions. It is currently composed of 194 species and 13 subspecies in eight genera: Amurodytes Fery & Petrov, 2013, Boreonectes Angus, 2010, Deronectes Sharp, 1882, Nebrioporus Régimbart, 1906, Oreodytes Seidlitz, 1887, Scarodytes Gozis, 1914, Stictotarsus Zimmermann, 1919, and Trichonectes Guignot, 1941. We present a morphological and a molecular phylogeny of the species of the subtribe, and a revision of their taxonomy to accommodate our phylogenetic results. The morphological phylogeny is based on the study of 54 characters of the adults of 189 species and 2 subspecies, of which 114 species and the 2 subspecies were coded in the morphological matrix. For the molecular phylogeny we investigated 115 species and 11 subspecies, using a combination of fragments of four mitochondrial (COI, 16S rRNA, tRNA-Leu and NAD1) and two nuclear genes (18S rRNA and H3), analysed with maximum likelihood and Bayesian methods. For both datasets we included the type species of all genus-group taxa. The morphological, molecular and combined phylogenies mostly agree with the current classification of the group, but in some cases our results are in contradiction with established genera. Most remarkable are the polyphyly of Stictotarsus and Nebrioporus, the low support for the monophyly and internal phylogeny of Oreodytes, and the low support for the monophyly of Deronectina with molecular data. Thus, we introduce some taxonomic changes in the current classification to accommodate the generic concepts to our phylogenetic results. Nine new genera are established: Clarkhydrus n. gen. (type species Hydroporus roffii Clark, 1862), Hornectes n. gen. (type species Hydroporus quadrimaculatus Horn, 1883), Iberonectes n. gen. (type species Deronectes bertrandi Legros, 1956), Larsonectes n. gen. (type species Potamonectes minipi Larson, 1991), Leconectes n. gen. (type species Hydroporus striatellus LeConte, 1852), Mystonectes n. gen. (type species Deronectes neomexicanus Zimmerman & Smith, 1975), Nectoboreus n. gen. (type species Hydroporus aequinoctialis Clark, 1862), Nectomimus n. gen. (type species Oreodytes okulovi Lafer, 1988), and Zaitzevhydrus n. gen. (type species Hydroporus formaster Zaitzev, 1908). Three genera are reinstated as valid: Deuteronectes Guignot, 1945 (stat. rest.) (type species Hydroporus picturatus Horn, 1883), Nectoporus Guignot, 1950 (stat. rest.) (type species Hydroporus abbreviatus Fall, 1923), and Neonectes J. Balfour-Browne, 1940 (stat. rest.) (type species Hydroporus natrix Sharp, 1884). Thirty-six new combinations for species and subspecies thus far treated in the genera Boreonectes, Nebrioporus, Oreodytes and Stictotarsus result from the new classification: Clarkhydrus corvinus (Sharp, 1887) n. comb., C. decemsignatus (Clark, 1862) n. comb., C. deceptus (Fall, 1932) n. comb., C. eximius (Motschulsky, 1859) n. comb., C. falli (Nilsson, 2001) n. comb., C. interjectus (Sharp, 1882) n. comb., C. minax (Zimmerman, 1982) n. comb., C. opaculus (Sharp, 1882) n. comb., C. roffii (Clark, 1862) n. comb., C. spectabilis (Zimmerman, 1982) n. comb., Deuteronectes angustior (Hatch, 1928) n. comb., Hornectes quadrimaculatus (Horn, 1883) n. comb., Iberonectes bertrandi (Legros, 1956) n. comb., Larsonectes minipi (Larson, 1991) n. comb., Leconectes striatellus (LeConte, 1852) n. comb., Mystonectes coelamboides (Fall, 1923) n. comb., M. grammicus (Sharp, 1887) n. comb., M. neomexicanus (Zimmerman & Smith, 1975) n. comb., M. panaminti (Fall, 1923) n. comb., M. titulus (Leech, 1945) n. comb., Nectoboreus aequinoctialis (Clark, 1862) n. comb., N. dolerosus (Leech, 1945) n. comb., N. funereus (Crotch, 1873) n. comb., Nectomimus okulovi (Lafer, 1988) n. comb., Nectoporus angelinii (Fery, 2015) n. comb., N. congruus (LeConte, 1878) n. comb., N. crassulus (Fall, 1923) n. comb., N. obesus obesus (LeConte, 1866) n. comb., N. obesus cordillerensis (Larson, 1990) n. comb., N. rhyacophilus (Zimmerman, 1985) n. comb., N. sanmarkii sanmarkii (C.R. Sahlberg, 1826) n. comb., N. sanmarkii alienus (Sharp, 1873) n. comb., N. sierrae (Zimmerman, 1985) n. comb., N. subrotundus (Fall, 1923) n. comb., Zaitzevhydrus formaster formaster (Zaitzev, 1908) n. comb., and Z. formaster ulanulana (C.-K. Yang, 1996) n. comb.

Text se zabývá historickým vývojem ústavního soudnictví na území ČR. V první části autor shrnuje vývoj myšlenky soudní kontroly ústavnosti právních předpisů a formuluje materiální předpoklady pro vytvoření ústavního soudu. Nad rámec požadavků formulovaných v dosavadní literatuře (psaná ústava, dělba moci, hierarchizace právního řádu) přidává autor ještě koncept suverenity lidu. Bez něj totiž nemůže fungovat filosofická obhajoba soudní kontroly ústavnosti jako ochrana zmocnitele (lidu) před excesy zmocněnce (parlamentu).Ve druhé části pak autor sleduje vývoj ústavního soudnictví v českém kontextu. Začíná u Říšského soudu zřízeného Prosincovou ústavou, který je některými autory pokládán za přímého předchůdce koncentrovaného a specializovaného ústavního soudu. Následně se zabývá obdobím první republiky označovaným Tomášem Langáškem jako promarněné světové prvenství. Analyzuje mimo jiné, proč činnost tohoto soudu výrazněji neovlivnila dobové dění a pravděpodobně byla i jedním z motivů, proč ústavní soudnictví nebylo po druhé světové válce obnoveno. Po intermezzu, kdy ústavní soudnictví buď neexistovalo, nebo sice bylo formálně zakotveno v právních předpisech, ale soud fakticky ustaven nebyl, sleduje autor vznik Ústavního soudu ČSFR a později též současného zákona č. 182/1993 Sb., o Ústavním soudu.

AbstractObjective: To determine trends in rates of nosocomial infections in Spanish hospitals.Design: Prospective prevalence studies, performed yearly from 1990 through 1994.Setting: A convenience sample of acute-care Spanish hospitals.Participants and Patients: The number of hospitals and patients included were as follows: 1990, 125 hospitals and 38,489 patients; 1991, 136 and 42,185; 1992, 163 and 44,343; 1993, 171 and 46,983; 1994, 186 and 49,689. A core sample of 74 hospitals, which participated in all five surveys and included a mean of 23,871 patients per year, was analyzed separately.Results: The overall prevalence rate of patients with nosocomial infections in the five studies was as follows: 1990, 8.5%; 1991, 7.8%; 1992, 7.3%; 1993, 7.1%; and 1994, 7.2%. The prevalence rate of patients with nosocomial infection in the core sample of 74 hospitals was 8.9%, 8.0%, 7.4%, 7.6%, and 7.6%, respectively (test for trend, P=.0001). Patients admitted to intensive care units had a 22.8% prevalence rate of nosocomial infection in 1994. The most common nosocomial infections by primary site were urinary tract infection and surgical site infections, followed by respiratory tract infections and bacteremia. More than 60% of all infections were supported by a microbiological diagnosis.Conclusions: The EPINE project provides a uniform tool for performing limited surveillance of nosocomial infections in most Spanish acute-care hospitals. Its use helps to spread an accepted set of definitions and methods for nosocomial infection control in the Spanish healthcare system. The surveys indicate that the prevalence of nosocomial infections has been reduced over the last 5 years in a core sample of Spanish hospitals.

-Sidney W. Mintz, Paget Henry ,C.L.R. James' Caribbean. Durham: Duke University Press, 1992. xvi + 287 pp., Paul Buhle (eds)-Allison Blakely, Jan M. van der Linde, Over Noach met zijn zonen: De Cham-ideologie en de leugens tegen Cham tot vandaag. Utrecht: Interuniversitair Instituut voor Missiologie en Oecumenica, 1993. 160 pp.-Helen I. Safa, Edna Acosta-Belén ,Researching women in Latin America and the Caribbean. Boulder CO: Westview, 1993. x + 201 pp., Christine E. Bose (eds)-Helen I. Safa, Janet H. Momsen, Women & change in the Caribbean: A Pan-Caribbean Perspective. Bloomington: Indiana University Press; Kingston: Ian Randle, 1993. x + 308 pp.-Paget Henry, Janet Higbie, Eugenia: The Caribbean's Iron Lady. London: Macmillan, 1993. 298 pp.-Kathleen E. McLuskie, Moira Ferguson, Subject to others: British women writers and Colonial Slavery 1670-1834. New York: Routledge, 1992. xii + 465 pp.-Samuel Martínez, Senaida Jansen ,Género, trabajo y etnia en los bateyes dominicanos. Santo Domingo: Instituto Tecnológico de Santo Domingo, Programa de Estudios se la Mujer, 1991. 195 pp., Cecilia Millán (eds)-Michiel Baud, Roberto Cassá, Movimiento obrero y lucha socialista en la República Dominicana (desde los orígenes hasta 1960). Santo Domingo: Fundación Cultural Dominicana, 1990. 620 pp.-Paul Farmer, Robert Lawless, Haiti's Bad Press. Rochester VT: Schenkman Press, 1992. xxvii + 261 pp.-Bill Maurer, Karen Fog Olwig, Global culture, Island identity: Continuity and change in the Afro-Caribbean Community of Nevis. Chur, Switzerland: Harwood Academic Publishers, 1993. xi + 239 pp.-Viranjini Munasinghe, Kevin A. Yelvington, Trinidad Ethnicity. Knoxville: University of Tennesee Press, 1993. vii + 296 pp.-Kevin K. Birth, Christine Ho, Salt-water Trinnies: Afro-Trinidadian Immigrant Networks and Non-Assimilation in Los Angeles. New York: AMS Press, 1991. xvi + 237 pp.-Steven Gregory, Andrés Isidoro Pérez y Mena, Speaking with the dead: Development of Afro-Latin Religion among Puerto Ricans in the United States. A study into the Interpenetration of civilizations in the New World. New York: AMS Press, 1991. xvi + 273 pp.-Frank Jan van Dijk, Mihlawhdh Faristzaddi, Itations of Jamaica and I Rastafari (The Second Itation, the Revelation). Miami: Judah Anbesa Ihntahnah-shinahl, 1991.-Derwin S. Munroe, Nelson W. Keith ,The Social Origins of Democratic Socialism in Jamaica. Philadelphia: Temple University Press, 1992. xxiv + 320 pp., Novella Z. Keith (eds)-Virginia Heyer Young, Errol Miller, Education for all: Caribbean Perspectives and Imperatives. Washington DC: Inter-American Development Bank, 1992. 267 pp.-Virginia R. Dominguez, Günter Böhm, Los sefardíes en los dominios holandeses de América del Sur y del Caribe, 1630-1750. Frankfurt: Vervuert, 1992. 243 pp.-Virginia R. Dominguez, Robert M. Levine, Tropical diaspora: The Jewish Experience in Cuba. Gainesville: University Press of Florida, 1993. xvii + 398 pp.-Aline Helg, John L. Offner, An unwanted war: The diplomacy of the United States and Spain over Cuba, 1895-1898. Chapel Hill: University of North Carolina Press, 1992. xii + 306 pp.-David J. Carroll, Eliana Cardoso ,Cuba after Communism. Cambridge MA: MIT Press, 1992. xiii + 148 pp., Ann Helwege (eds)-Antoni Kapcia, Ian Isadore Smart, Nicolás Guillén: Popular Poet of the Caribbean. Columbia: University of Missouri Press, 1990. 187 pp.-Sue N. Greene, Moira Ferguson, The Hart Sisters: Early African Caribbean Writers, Evangelicals, and Radicals. Lincoln: University of Nebraska Press, 1993. xi + 214 pp.-Michael Craton, James A. Lewis, The final campaign of the American revolution: Rise and fall of the Spanish Bahamas. Columbia: University of South Carolina Press, 1991. xi + 149 pp.-David Geggus, Clarence J. Munford, The black ordeal of slavery and slave trading in the French West Indies, 1625-1715. Lewiston NY: The Edwin Mellen Press, 1991. 3 vols. xxii + 1054 pp.-Paul E. Sigmund, Timothy P. Wickham-Crowley, Guerillas and Revolution in Latin America: A comparative Study of Insurgents and Regimes since 1956. Princeton: Princeton University Press, 1992. xx + 424 pp.-Robert E. Millette, Patrick A.M. Emmanuel, Elections and Party Systems in the Commonwealth Caribbean, 1944-1991. St. Michael, Barbados: Caribbean Development Research Services, 1992. viii + 111 pp.-Robert E. Millette, Donald C. Peters, The Democratic System in the Eastern Caribbean. Westport CT: Greenwood Press, 1992. xiv + 242 pp.-Pedro A. Cabán, Arnold H. Liebowitz, Defining status: A comprehensive analysis of United States Territorial Relations. Boston & Dordrecht: Martinus Nijhoff, 1989. xxii + 757 pp.-John O. Stewart, Stuart H. Surlin ,Mass media and the Caribbean. New York: Gordon & Breach, 1990. xviii + 471 pp., Walter C. Soderlund (eds)-William J. Meltzer, Antonio V. Menéndez Alarcón, Power and television in Latin America: The Dominican Case. Westport CT: Praeger, 1992. 199 pp.

A total of 2 741 individuals belonging to 185 species were collected from 2004 to 2006. This material included several rare species out of which 5 are new to the fauna of the Baranya country: Dyschirius tristis Stephens, 1827, Pogonus transfuga peisonis (Ganglbauer, 1892), Amara gebleri Dejean, 1831, Ophonus subsinuatus Rey, 1886, Harpalus albanicus Reitter, 1900. Besides, the comments of 10 rare species are given. In this article a total of 214 species are listed, the earlier data coming from J. SÁR (1992, 1993, 1995) and P. SÁR (2005).

The paper represents the first part of a project dealing with the Finnish Pipunculidae fauna and focuses on certain taxonomic aspects of the genera Cephalops Fallén, 1810, Pipunculus Latreille, 1802 and Tomosvaryella Aczél, 1939. Tomosvaryella kalevala Kehlmaier spec. nov. is described as new to science and its male and female terminalia are figured. Lectotypes are designated for Pipunculus ater Meigen, 1824, Pipunculus calceatus Roser, 1840, Pipunculus campestris Latreille, 1802, Pipunculus chlorionae Frey, 1945, Pipunculus dentipes Meigen, 1838, Pipunculus elegans Egger, 1860, Pipunculus oldenbergi Collin, 1956, Pipunculus spinipes Meigen, 1830, Pipunculus thomsoni Becker, 1897, Pipunculus varipes Meigen, 1824, Pipunculus wolfi Kowarz, 1887 and Pipunculus zugmayeriae Kowarz, 1887. Pipunculus elegans and P. wolfi are resurrected from synonymy (stat. rev.). Pipunculus varipes is transferred to Cephalops (comb. nov.). The following new synonymies are proposed (syn. nov.): Cephalops semifumosus (Kowarz, 1887) = Cephalops varipes (Meigen, 1824), P. spinipes and P. thomsoni = P. campestris, Pipunculus balticus Kuznetzov, 1991 = Pipunculus tenuirostris Kozánek, 1981, Pipunculus phaeton Coe, 1966 and Pipunculus nartshukae Kuznetzov, 1990 = P. omissinervis Becker, 1889, Tomosvaryella magyarica Földvári & De Meyer, 1999 = Tomosvaryella minuscula (Collin, 1956). The European representatives of Pipunculus are characterized, their terminalia partly figured and the taxa keyed out in an dichotomous identification key. Tomosvaryella rossica Kuznetzov, 1993 and Tomosvaryella cilitarsis (Strobl, 1910) are partly figured and, together with T. kalevala Kehlmaier spec. nov., incorporated into the identification key of Földvári & De Meyer (1999).

Analisou-se oito experimentos realizados em áreas irrigadas do Submédio São Francisco, entre os anos de 1988 e 1993, com o objetivo de relacionar a resposta do tomateiro industrial (Lycopersicon esculentum, Mill) à adubação fosfatada em solos com diferentes teores de fósforo disponível determinado pelos métodos Mehlich-1 ou Bray-1. Nos solos com conteúdo de P disponível igual ou inferior a 2 mg.dm-3, os aumentos em produtividade, provocados pela adubação foram, em média, de 190,8%, enquanto no solo com teor de P de 8 mg.dm-3, o aumento foi de apenas 21,7%. Porém, em solos com teor de P igual ou superior a 14 mg dm-3, não foi verificada resposta do tomateiro à adubação fosfatada. Para os dois experimentos onde foi possível ajustar equações quadráticas, as produtividades máximas econômicas de tomate (56,47 e 69,35 t.ha-1) foram obtidas com os níveis de 143 e 182 kg.ha-1 de P2O5, respectivamente.

Epidemiological characteristics of canine rabies in the northwest region of São Paulo State (Araçatuba region), Brazil, from 1993 to 1997 are presented. Out of 1,984 dogs, a total of 351 (17.7%) were positive for rabies diagnosis; 89% (312/351) of these occurred in urban areas and 85% (266/312) of the urban positive cases were among owned dogs. The mean age of the rabid dogs was 34 months and 61% were male. Aggressive behavior was observed in 77% of rabid dogs, followed by lack of coordination and paralysis (42%) and 48% of these dogs were responsible biting people or other animals. Information about vaccination status was obtained from 182 records and 51% of rabid dogs were non-vaccinated. The number of unvaccinated rabid dogs indicates a low vaccination index and this factor added to the high dog/man ratio must have contributed to the canine rabies epizootic observed in the studied area.

Since 1993 the Federal Drug Administration approved the use of immunomodulatory therapy in multiple sclerosis (MS), modifying the natural course of disease, as demonstrate our experience in treatment of MS patients at the MS Treatment Center (CATEM). OBJECTIVE: To evaluate patient behavior using immunomodulatory therapy for a period of five years treatment. METHOD: We selected 390 patients in CATEM with relapsing-remitting MS (RRMS) and secondary progressive MS (SPMS) with relapses. RESULTS: At initial treatment 292 (61.5%) patients presented RRMS, 98 (20.6%) SPMS with relapses, 27 SPMS (5.6%) and 58 (12.1%) primary progressive MS (PPMS). In RRMS 182 (62.5%) used the interferon beta 1a SC, 15 (5.2%) interferon beta 1a IM, 85 (29%) interferon beta 1b and 10 (3.3%) glatiramer acetate. In SPMS 63 (64.3%) used interferon beta 1a SC, 4 (4.1%) interferon beta 1a IM and 31 (31.4%) interferon beta 1b. We observed that in this period 195 (50%) migrated between drugs, 35 (9%) gave up therapy and 160 (41%) continued the initial therapy. CONCLUSION: Stopping the immunomodulatory therapy emerges as a problem in the second year of treatment and it can be a subset of interferon non responsive or development of neutralizing antibodies.

The Diptera genus-group names of Johann Wilhelm Meigen are reviewed, revised, and annotated. A total of 266 available genus-group names in 69 families of Diptera are listed alphabetically, including authorship, year and page of the original publication, originally included species, type species and method of fixation, current status of the name, family placement, and any emendations that have been found in the literature. Unavailable names suppressed by ICZN rulings as well as incorrect original and subsequent spellings are included as unnumbered entries. Remarks are given to clarify nomenclatural or taxonomic information. In addition, an index to all the species-group names of Diptera proposed by Meigen (3,117 in total, of which 2,966 are available) is given with a bibliographic reference to each original citation. An appendix gives a complete bibliography of all the known published writings by Meigen, non-zoological as well as zoological. The following type species designation is proposed: Dasypogon priscus Meigen, 1820 for Podoctria Meigen, 1820, by present designation [Asilidae]. First Reviser actions for multiple original spellings that have not previously been recognized (viz., those made via ICZN Code Art. 24.2.4) or are made herein are given for the following: Chrysotus Meigen, 1824 [Dolichopodidae]; Ocydromia Meigen, 1820 [Hybotidae]; Rhamphomyia Meigen, 1822 [Empididae]; Tachypeza Meigen, 1830a [Hybotidae]. Earlier valid subsequent type-species designations have been found for the following: Ascia Meigen, 1822 [Syrphidae]; Borborus Meigen, 1803 [Sphaeroceridae]; Brachygaster Meigen, 1826 [Sepsidae]; Cephalia Meigen, 1826 [Ulidiidae]; Chrysotus Meigen, 1824 [Dolichopodidae]; Ctenophora Meigen, 1803 [Tipulidae]; Diastata Meigen, 1830a [Diastatidae]; Doros Meigen, 1803 [Syrphidae]; Erioptera Meigen, 1803 [Limoniidae]; Glochina Meigen, 1830a [Limoniidae]; Macrocera Meigen, 1803 [Keroplatidae]; Merodon Meigen, 1803 [Syrphidae]; Mesembrina Meigen, 1826 [Muscidae]; Mycetobia Meigen, 1818a [Anisopodidae]; Odontomyia Meigen, 1803 [Stratiomyidae]; Oedalea Meigen, 1820 [Hybotidae]; Phania Meigen, 1824 [Tachinidae]; Platypeza Meigen, 1803 [Platypezidae]; Platyptera Meigen, 1803 [Empididae]; Platyura Meigen, 1803 [Keroplatidae]; Spilomyia Meigen, 1803 [Syrphidae]; Stegana Meigen, 1830a [Drosophilidae]; Trineura Meigen, 1803 [Phoridae]; Ulidia Meigen, 1826 [Ulidiidae]; Xysta Meigen, 1824 [Tachinidae]. The following type species are fixed herein under ICZN Code Article 70.3.2: Rhagio ibis Fabricius, 1775 for Atherix Meigen, 1803 [Athericidae]; Coelopa pilipes Haliday, 1838 for Coelopa Meigen, 1803 [Coelopidae]; Diastata vagans Loew, 1864 for Diastata Meigen, 1803 [Diastatidae]; Tanypus punctipennis Meigen, 1818a for Tanypus Meigen, 1803 [Chironomidae]. Corrected or clarified nomenclatural status, included species, and/or corrected or clarified type-species are given for: Acrocera Meigen, 1803 [Acroceridae]; Aedes Meigen, 1818a [Culicidae]; Anisomera Meigen, 1818a [Limoniidae]; Ascia Meigen, 1822 [Syrphidae]; Atherix Meigen, 1803 [Athericidae]; Bactria Meigen, 1820 [Asilidae]; Bolitophila Meigen, 1818a [Bolitophilidae]; Borborus Meigen, 1803 [Chloropidae]; Brachygaster Meigen, 1826 [Sepsidae]; Cephalia Meigen, 1826 [Ulidiidae]; Chlorops Meigen, 1803 [Chloropidae]; Chrysotoxum Meigen, 1803 [Syrphidae]; Chrysotus Meigen, 1824 [Dolichopodidae]; Coelopa Meigen, 1830a [Coelopidae]; Ctenophora Meigen, 1803 [Tipulidae]; Dialyta Meigen, 1826 [Muscidae]; Diastata Meigen, 1830a [Diastatidae]; Dictya Meigen, 1803 [Sciomyzidae]; Diomyza Meigen, 1818a [Cecidomyiidae]; Doros Meigen, 1803 [Syrphidae]; Dorycera Meigen, 1830a [Ulidiidae]; Erioptera Meigen, 1803 [Limoniidae]; Furcomyia Meigen, 1818a [Limoniidae]; Glochina Meigen, 1830a [Limoniidae]; Hexacantha Meigen, 1803 [Stratiomyidae]; Hexatoma Meigen, 1818a [Tabanidae]; Lasiops Meigen, 1838 [Muscidae]; Leptina Meigen, 1822 [Tipulidae]; Leptocera Meigen, 1818a [Bolitophilidae]; Leucopis Meigen, 1830a, [Chamaemyiidae]; Loxocera Meigen, 1803 [Psilidae]; Macrocera Meigen, 1803 [Keroplatidae]; Marginomyia Meigen, 1818a [Limoniidae]; Merodon Meigen, 1803 [Syrphidae]; Mesembrina Meigen, 1826 [Muscidae]; Mima Meigen, 1820 [Bombyliidae]; Mycetobia Meigen, 1818a [Anisopodidae]; Nematocera Meigen, 1818a [Limoniidae]; Nodutis Meigen, 1820 [Athericidae]; Odontomyia Meigen, 1803 [Stratiomyidae]; Oedalea Meigen, 1820 [Hybotidae]; Pelecocera Meigen, 1822 [Syrphidae]; Phalangus Meigen, 1822 [Syrphidae]; Phania Meigen, 1824 [Tachinidae]; Platypeza Meigen, 1803 [Platypezidae]; Platyptera Meigen, 1803 [Empididae]; Platyura Meigen, 1803 [Keroplatidae]; Podoctria Meigen, 1820 [Asilidae]; Psilopus Meigen, 1824 [Dolichopodidae]; Sarcophaga Meigen, 1824 [Sarcophagidae]; Stegana Meigen, 1830a [Drosophilidae]; Subula Meigen, 1820 [Xylomyidae]; Tanyglossa Meigen, 1803 [Tabanidae]; Tanypus Meigen, 1803 [Chironomidae]; Therina Meigen, 1830a [Heleomyzidae]; Trineura Meigen, 1803 [Phoridae]; Ulidia Meigen, 1826 [Ulidiidae]; Unomyia Meigen, 1818a [Limoniidae]; Xylota Meigen, 1822 [Syrphidae]; Xysta Meigen, 1824 [Tachinidae]. New synonymies are proposed for the following genus-group names: Melanopangonius Szilády, 1923 under Tanyglossa Meigen, 1803, n. syn. [Tabanidae]; Planuria Meigen, 1826 under Homalura Meigen, 1826, n. syn. [Chloropidae]; Polimera Meigen, 1826 under Polymera Wiedemann, 1820, n. syn. [Limoniidae]; Trepidaria Swinderen, 1822 under Seioptera Kirby & Spence, 1817, n. syn. [Ulidiidae]. Reversal of precedence (Code Article 23.9.2) is invoked in two instances to promote stability in nomenclature. One for homonymy: Sarcophaga Meigen, 1824, nomen protectum [in Sarcophagidae] and Sarcophaga Swinderen, 1822, nomen oblitum [in Calliphoridae]; and one for objective synonymy: Calliphora Robineau-Desvoidy, 1830, nomen protectum and Sarcophaga Swinderen, 1822, nomen oblitum [in Calliphoridae].

A review of genus-group names for darkling beetles in the family Tenebrionidae (Insecta: Coleoptera) is presented. A catalogue of 4122 nomenclaturally available genus-group names, representing 2307 valid genera (33 of which are extinct) and 761 valid subgenera, is given. For each name the author, date, page number, gender, type species, type fixation, current status, and first synonymy (when the name is a synonym) are provided. Genus-group names in this family are also recorded in a classification framework, along with data on the distribution of valid genera and subgenera within major biogeographical realms. A list of 535 unavailable genus-group names (e.g., incorrect subsequent spellings) is included. Notes on the date of publication of references cited herein are given, when known. The following genera and subgenera are made available for the first time: Anemiadena Bouchard &amp; Bousquet, subgen. nov. (in Cheirodes Gené, 1839), Armigena Bouchard &amp; Bousquet, subgen. nov. (in Nesogena Mäklin, 1863), Debeauxiella Bouchard &amp; Bousquet, subgen. nov. (in Hyperops Eschscholtz, 1831), Hyperopsis Bouchard &amp; Bousquet, subgen. nov. (in Hyperops Eschscholtz, 1831), Linio Bouchard &amp; Bousquet, subgen. nov. (in Nilio Latreille, 1802), Matthewsotys Bouchard &amp; Bousquet, gen. nov., Neosolenopistoma Bouchard &amp; Bousquet, subgen. nov. (in Eurynotus W. Kirby, 1819), Paragena Bouchard &amp; Bousquet, subgen. nov. (in Nesogena Mäklin, 1863), Paulianaria Bouchard &amp; Bousquet, gen. nov., Phyllechus Bouchard &amp; Bousquet, gen. nov., Prorhytinota Bouchard &amp; Bousquet, subgen. nov. (in Rhytinota Eschscholtz, 1831), Pseudorozonia Bouchard &amp; Bousquet, subgen. nov. (in Rozonia Fairmaire, 1888), Pseudothinobatis Bouchard &amp; Bousquet, gen. nov., Rhytinopsis Bouchard &amp; Bousquet, subgen. nov. (in Thalpophilodes Strand, 1942), Rhytistena Bouchard &amp; Bousquet, subgen. nov. (in Rhytinota Eschscholtz, 1831), Spinosdara Bouchard &amp; Bousquet, subgen. nov. (in Osdara Walker, 1858), Spongesmia Bouchard &amp; Bousquet, subgen. nov. (in Adesmia Fischer, 1822), and Zambesmia Bouchard &amp; Bousquet, subgen. nov. (in Adesmia Fischer, 1822). The names Adeps Gistel, 1857 and Adepsion Strand, 1917 syn. nov. [= Tetraphyllus Laporte &amp; Brullé, 1831], Asyrmatus Canzoneri, 1959 syn. nov. [= Pystelops Gozis, 1910], Euzadenos Koch, 1956 syn. nov. [= Selenepistoma Dejean, 1834], Gondwanodilamus Kaszab, 1969 syn. nov. [= Conibius J.L. LeConte, 1851], Gyrinodes Fauvel, 1897 syn. nov. [= Nesotes Allard, 1876], Helopondrus Reitter, 1922 syn. nov. [= Horistelops Gozis, 1910], Hybonotus Dejean, 1834 syn. nov. [= Damatris Laporte, 1840], Iphthimera Reitter, 1916 syn. nov. [= Metriopus Solier, 1835], Lagriomima Pic, 1950 syn. nov. [= Neogria Borchmann, 1911], Orphelops Gozis, 1910 syn. nov. [= Nalassus Mulsant, 1854], Phymatium Billberg, 1820 syn. nov. [= Cryptochile Latreille, 1828], Prosoblapsia Skopin &amp; Kaszab, 1978 syn. nov. [= Genoblaps Bauer, 1921], and Pseudopimelia Gebler, 1859 syn. nov. [= Lasiostola Dejean, 1834] are established as new synonyms (valid names in square brackets). Anachayus Bouchard &amp; Bousquet, nom. nov. is proposed as a replacement name for Chatanayus Ardoin, 1957, Genateropa Bouchard &amp; Bousquet, nom. nov. as a replacement name for Apterogena Ardoin, 1962, Hemipristula Bouchard &amp; Bousquet, nom. nov. as a replacement name for Hemipristis Kolbe, 1903, Kochotella Bouchard &amp; Bousquet, nom. nov. as a replacement name for Millotella Koch, 1962, Medvedevoblaps Bouchard &amp; Bousquet, nom. nov. as a replacement name for Protoblaps G.S. Medvedev, 1998, and Subpterocoma Bouchard &amp; Bousquet, nom. nov. is proposed as a replacement name for Pseudopimelia Motschulsky, 1860. Neoeutrapela Bousquet &amp; Bouchard, 2013 is downgraded to a subgenus (stat. nov.) of Impressosora Pic, 1952. Anchomma J.L. LeConte, 1858 is placed in Stenosini: Dichillina (previously in Pimeliinae: Anepsiini); Entypodera Gerstaecker, 1871, Impressosora Pic, 1952 and Xanthalia Fairmaire, 1894 are placed in Lagriinae: Lagriini: Statirina (previously in Lagriinae: Lagriini: Lagriina); Loxostethus Triplehorn, 1962 is placed in Diaperinae: Diaperini: Diaperina (previously in Diaperinae: Diaperini: Adelinina); Periphanodes Gebien, 1943 is placed in Stenochiinae: Cnodalonini (previously in Tenebrioninae: Helopini); Zadenos Laporte, 1840 is downgraded to a subgenus (stat. nov.) of the older name Selenepistoma Dejean, 1834. The type species [placed in square brackets] of the following available genus-group names are designated for the first time: Allostrongylium Kolbe, 1896 [Allostrongylium silvestre Kolbe, 1896], Auristira Borchmann, 1916 [Auristira octocostata Borchmann, 1916], Blapidocampsia Pic, 1919 [Campsia pallidipes Pic, 1918], Cerostena Solier, 1836 [Cerostena deplanata Solier, 1836], Coracostira Fairmaire, 1899 [Coracostira armipes Fairmaire, 1899], Dischidus Kolbe, 1886 [Helops sinuatus Fabricius, 1801], Eccoptostoma Gebien, 1913 [Taraxides ruficrus Fairmaire, 1894], Ellaemus Pascoe, 1866 [Emcephalus submaculatus Brême, 1842], Epeurycaulus Kolbe, 1902 [Epeurycaulus aldabricus Kolbe, 1902], Euschatia Solier, 1851 [Euschatia proxima Solier, 1851], Heliocaes Bedel, 1906 [Blaps emarginata Fabricius, 1792], Hemipristis Kolbe, 1903 [Hemipristis ukamia Kolbe, 1903], Iphthimera Reitter, 1916 [Stenocara ruficornis Solier, 1835], Isopedus Stein, 1877 [Helops tenebrioides Germar, 1813], Malacova Fairmaire, 1898 [Malacova bicolor Fairmaire, 1898], Modicodisema Pic, 1917 [Disema subopaca Pic, 1912], Peltadesmia Kuntzen, 1916 [Metriopus platynotus Gerstaecker, 1854], Phymatium Billberg, 1820 [Pimelia maculata Fabricius, 1781], Podoces Péringuey, 1886 [Podoces granosula Péringuey, 1886], Pseuduroplatopsis Pic, 1913 [Borchmannia javana Pic, 1913], Pteraulus Solier, 1848 [Pteraulus sulcatipennis Solier, 1848], Sciaca Solier, 1835 [Hylithus disctinctus Solier, 1835], Sterces Champion, 1891 [Sterces violaceipennis Champion, 1891] and Teremenes Carter, 1914 [Tenebrio longipennis Hope, 1843]. Evidence suggests that some type species were misidentified. In these instances, information on the misidentification is provided and, in the following cases, the taxonomic species actually involved is fixed as the type species [placed in square brackets] following requirements in Article 70.3 of the International Code of Zoological Nomenclature: Accanthopus Dejean, 1821 [Tenebrio velikensis Piller &amp; Mitterpacher, 1783], Becvaramarygmus Masumoto, 1999 [Dietysus nodicornis Gravely, 1915], Heterophaga Dejean, 1834 [Opatrum laevigatum Fabricius, 1781], Laena Dejean, 1821, [Scaurus viennensis Sturm, 1807], Margus Dejean, 1834 [Colydium castaneum Herbst, 1797], Pachycera Eschscholtz, 1831 [Tenebrio buprestoides Fabricius, 1781], Saragus Erichson, 1842 [Celibe costata Solier, 1848], Stene Stephens, 1829 [Colydium castaneum Herbst, 1797], Stenosis Herbst, 1799 [Tagenia intermedia Solier, 1838] and Tentyriopsis Gebien, 1928 [Tentyriopsis pertyi Gebien, 1940]. The following First Reviser actions are proposed to fix the precedence of names or nomenclatural acts (rejected name or act in square brackets): Stenosis ciliaris Gebien, 1920 as the type species for Afronosis G.S. Medvedev, 1995 [Stenosis leontjevi G.S. Medvedev, 1995], Alienoplonyx Bremer, 2019 [Alienolonyx], Amblypteraca Mas-Peinado, Buckley, Ruiz &amp; García-París, 2018 [Amplypteraca], Caenocrypticoides Kaszab, 1969 [Caenocripticoides], Deriles Motschulsky, 1872 [Derilis], Eccoptostira Borchmann, 1936 [Ecoptostira], †Eodromus Haupt, 1950 [†Edromus], Eutelus Solier, 1843 [Lutelus], Euthriptera Reitter, 1893 [Enthriptera], Meglyphus Motschulsky, 1872 [Megliphus], Microtelopsis Koch, 1940 [Extetranosis Koch, 1940, Hypermicrotelopsis Koch, 1940], Neandrosus Pic, 1921 [Neoandrosus], Nodosogylium Pic, 1951 [Nodosogilium], Notiolesthus Motschulsky, 1872 [Notiolosthus], Pseudeucyrtus Pic, 1916 [Pseudocyrtus], Pseudotrichoplatyscelis Kaszab, 1960 [Pseudotrichoplatynoscelis and Pseudotrichoplatycelis], Rhydimorpha Koch, 1943 [Rhytimorpha], Rhophobas Motschulsky, 1872 [Rophobas], Rhyssochiton Gray, 1831 [Ryssocheton and Ryssochiton], Sphaerotidius Kaszab, 1941 [Spaerotidius], Stira Agassiz, 1846 (Mollusca) [Stira Agassiz, 1846 (Coleoptera)], Sulpiusoma Ferrer, 2006 [Sulpiosoma] and Taenobates Motschulsky, 1872 [Taeniobates]. Supporting evidence is provided for the conservation of usage of Cyphaleus Westwood, 1841 nomen protectum over Chrysobalus Boisduval, 1835 nomen oblitum.

Abstract The time and velocity of ejection of dust particles of anomalous tails from cometary nuclei are determined. It is revealed that some comets cause the formation of an anomalous tail is the collision of their comet nucleus with other bodies of the Solar System. An investigation of the formation conditions of the anomalous tail shows that the dust ejection velocity from the comet nucleus C/1851 U1, C/1885 X2, C/1921 E1, C/1925 V1, C/1930 D1, C/1975 V2, 2P/1924, 6P/1950 and 1976, 10P/1930, 7P/1933 and 35P/1939 O1 can be explained by the sublimation of the ice of the nucleus and the removal of dust by molecules. It was found that the comets C/1823 Y1, C/1882 R1, C/1883 D1, C/1888 R1, C/1892 E1, D/1894 F1, C/1932 M1, C/1954 O1, C/1968 H1, C/1969 T1, C/1973 E1, C/1995 O1, C/1999 S4, C/2004 Q2, 7P/1869 G1, 10P/1930, 19P/1918, 26P/1927 F1, 67P/1982, 73P/1930 J1, 96P/1986 J1 and 109P/1862 O1, formation of the anomalous tail and splitting of the comet nucleus was observed in one appearance. Nuclear splitting 70% of these comets occurred as a result of a collision of the comet’s nucleus with a meteoroid or fragments of their nuclei.

The type material of three Spanish and two Moroccan taxa of Curculionidae is studied and its identity is assessed, resulting in the following new synonymies: Sciaphilus Schoenherr, 1823 = Elevatosomus Zumpt, 1933; Sciaphilus costulatus Kiesenwetter, 1852 = Eusomus (Elevatosomus) freyi Zumpt, 1933; Pachyrhinus Schoenherr, 1823 = Parisodrosus Voss, 1936; Pachyrhinus javeti (Desbrochers, 1871) = Polydrosus (Parisodrosus) balearicus Voss, 1936; Larinus Dejean, 1821 = Rungsonymus Hoffmann, 1950; Larinus (Larinus) buccinator (Olivier, 1807) = Rungsonymus ambiguus Hoffmann, 1950; Lixoglyptus Reitter, 1916 = Resmecaspis Hoffmann, 1959; Lixus (Lixoglyptus) spartii Olivier, 1807 = Mecaspis (Resmecaspis) pecoudi Hoffmann, 1959; Neseremnus Marshall, 1921 = Kocheriana Hoffmann, 1953. Lixoglyptus Reitter, 1916 is raised to genus (stat. prom.) and transferred from Lixini to Cleonini (new placement). Three species are transferred to other genera: Lixoglyptus spartii (Olivier, 1807) comb. n., Lixoglyptus mogadorus (Heyden, 1887) comb. n. and Neseremnus grassellyi (Hoffmann, 1953) comb. n. A lectotype is designated for Polydrosus (Parisodrosus) balearicus Voss, 1936.

El estudio de la dinámica del uso del suelo permite conocer el usufructo, manejo y aprovechamiento que el hombre hace de la naturaleza, además de realizar la predicción de su tendencia que fundamente la toma de decisiones para el mejor empleo del territorio. La metodología aplicada en el trabajo que se describe consistió en detectar cambios en el uso del suelo mediante el análisis de fotografías aéreas e imágenes satelitales de 1993 y 2004. Posteriormente, se recurrió a conceptos y técnicas de evaluación multicriterio espacial, lógica difusa, autómatas celulares y cadenas de Markov para modelar el escenario del cambio de uso al 2014. Los resultados para el periodo 1993-2004 indican un aumento en la extensión del uso urbano de 173 ha, minero de 92 ha, cuerpos de agua de 3 ha y una disminución en los usos agrícolas de 182 ha, pastizal inducido de 64 ha, bosque 14 ha, en áreas de reforestación 7 ha y pastizal natural 1 ha. La proyección para el 2014 señala incrementos en la superficie urbana 154 ha, minería 81 ha y pastizal natural 13 ha; las áreas que se reducirán son: la agrícola 165 ha, pastizal inducido 56 ha, bosque 23 ha, y reforestación 6 ha. Los usos urbano y minero crecerían en prejuicio de los agrícola, pastizal inducido, y en menor medida, hacia el bosque y las zonas de reforestación. El uso urbano crece a una tasa anual de 15.7 ha y 15 ha en el primer periodo y para el proyectado, respectivamente.

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Boulder CO: Lynne Rienner, 1993, xii + 263 pp.-G.B. Hagelberg, Scott B. MacDonald ,The politics of the Caribbean basin sugar trade. New York: Praeger, 1991. vii + 164 pp., Georges A. Fauriol (eds)-Bonham C. Richardson, Trevor W. Purcell, Banana Fallout: Class, color, and culture among West Indians in Costa Rica. Los Angeles: UCLA Center for Afro-American studies, 1993. xxi + 198 pp.-Gertrude Fraser, George Gmelch, Double Passage: The lives of Caribbean migrants abroad and back home. Ann Arbor: University of Michigan Press, 1992. viii + 335 pp.-Gertrude Fraser, John Western, A passage to England: Barbadian Londoners speak of home. Minneapolis: University of Minnesota Press, 1992. xxii + 309 pp.-Trevor W. Purcell, Harry G. Lefever, Turtle Bogue: Afro-Caribbean life and culture in a Costa Rican Village. Cranbury NJ: Susquehanna University Press, 1992. 249 pp.-Elizabeth Fortenberry, Virginia Heyer Young, Becoming West Indian: Culture, self, and nation in St. Vincent. Washington DC: Smithsonian Institution Press, 1993. x + 229 pp.-Horace Campbell, Dudley J. Thompson ,From Kingston to Kenya: The making of a Pan-Africanist lawyer. Dover MA: The Majority Press, 1993. xii + 144 pp., Margaret Cezair Thompson (eds)-Kumar Mahabir, Samaroo Siewah, The lotus and the dagger: The Capildeo speeches (1957-1994). Port of Spain: Chakra Publishing House, 1994. 811 pp.-Donald R. Hill, Forty years of steel: An annotated discography of steel band and Pan recordings, 1951-1991. Jeffrey Thomas (comp.). Westport CT: Greenwood, 1992. xxxii + 307 pp.-Jill A. Leonard, André Lucrèce, Société et modernité: Essai d'interprétation de la société martiniquaise. Case Pilote, Martinique: Editions de l'Autre Mer, 1994. 188 pp.-Dirk H. van der Elst, Ben Scholtens ,Gaama Duumi, Buta Gaama: Overlijden en opvolging van Aboikoni, grootopperhoofd van de Saramaka bosnegers. Stanley Dieko. Paramaribo: Afdeling Cultuurstudies/Minov; Amsterdam: Koninklijk Instituut voor de Tropen, 1992. 204 pp., Gloria Wekker, Lady van Putten (eds)-Rosemarijn Hoefte, Chandra van Binnendijk ,Sranan: Cultuur in Suriname. Amsterdam: Koninklijk Instituut voor de Tropen/Rotterdam: Museum voor Volkenkunde, 1992. 159 pp., Paul Faber (eds)-Harold Munneke, A.J.A. Quintus Bosz, Grepen uit de Surinaamse rechtshistorie. Paramaribo: Vaco, 1993. 176 pp.-Harold Munneke, Irvin Kanhai ,Strijd om grond in Suriname: Verkenning van het probleem van de grondenrechten van Indianen en Bosnegers. Paramaribo, 1993, 200 pp., Joyce Nelson (eds)-Ronald Donk, J. Hartog, De geschiedenis van twee landen: De Nederlandse Antillen en Aruba. Zaltbommel: Europese Bibliotheek, 1993. 183 pp.-Aart G. Broek, J.J. Oversteegen, In het schuim van grauwe wolken: Het leven van Cola Debrot tot 1948. Amsterdam: Muelenhoff, 1994. 556 pp.''Gemunt op wederkeer: Het leven van Cola Debrot vanaf 1948. Amsterdam: Muelenhoff, 1994. 397 pp.

The genus Sitticus Simon, 1901 sensu lato is revised and split into new genera Sittiab gen. n., Sittiflor gen. n., Sittilong gen. n., Sittisax gen. n., which join existing already Attulus Simon, 1889 sensu novo, Jollas Simon, 1901, Sitticus Simon, 1901 sensu stricto, and Sittipub Prószyński, 2016, based on interpretation of taxonomic data from a number of publications of the Author, on the background of world's literature synthesized in Prószyński (2016a, b) available at http://www.peckhamia.com/salticidae/Subfamilies/, and http://www.peckhamia.com/salticidae/.The following new synonyms and combinations are established, or clarified. Attus viduus Kulczyński, 1895 (removed from synonymy of A. distinguendus) = Attulus avocator (O. Pickard-Cambridge, 1885) comb. n., Jollas armatus (Bryant, 1943) = "Oningis" armatus Bryant, 1943b - retransfer of misplaced species, belonging to EUOPHRYINES, Jollas crassus (Bryant, 1943) = "Oningis" crassus Bryant, 1943 - retransfer of misplaced species, belonging to EUOPHRYINES, Jollas lahorensis (Dyal, 1935) (nomen dubium) = "Oningis" lahorensis Dyal, 1935 - unrecognizable species, should be listed as nomen dubium in its original combination, Sitticus absolutus (Gertsch, Mulaik, 1936) = Sittiab absolutus (Gertsch & Mulaik, 1936) comb. n., Sitticus ammophilus (Thorell, 1875) = Attulus ammophilus (Thorell, 1875) comb. n., Sitticus ansobicus Andreeva, 1976 = Attulus ansobicus (Andreeva, 1976) comb. n., Sitticus atricapillus (Simon, 1882) = Sittiflor atricapillus (Simon, 1882) comb. n., Sitticus avocator (Pickard-Cambridge O., 1885) = Attulus avocator (Pickard-Cambridge O., 1885) comb. n., Sitticus burjaticus Danilov & Logunov, 1993 = Attulus burjaticus (Danilov & Logunov, 1993) comb. n., Sitticus caricis (Westring, 1861) = Sittiflor caricis (Westring, 1861) comb. n., Sitticus clavator Schenkel, 1936 = Attulus clavator (Schenkel, 1936) comb. n., Sitticus concolor: Maddison, 1996 (nomen dubium) = Sittiab cursor (Barrows, 1919) comb. n., Sitticus cursor (Barrows, 1919) = Sittiab cursor (Barrows, 1919) comb. n., Sitticus cutleri Prószynski, 1980 = Sittiflor cutleri (Prószynski, 1980) comb. n., Sitticus damini (Chyzer & Kulczynski, 1891) = Attulus damini (Chyzer & Kulczynski, 1891) comb. n., Sitticus distinguendus (Simon, 1868) = Attulus distinguendus (Simon, 1868) comb. n., Sitticus dorsatus: Richman, 1979 (nomen dubium) = Sittiab absolutus Gertsch & Mulaik, 1936 comb. n., Sitticus dubatolovi Logunov & Rakov, 1998 = Attulus dubatolovi (Logunov & Rakov, 1998) comb. n., Sitticus dudkoi Logunov, 1998 = Sittiflor dudkoi (Logunov, 1998) comb. n., Sitticus dzieduszyckii (L. Koch, 1870) = Sittisax dzieduszyckii (L. Koch, 1870) comb. n., Sitticus floricola (Koch C.L., 1837) = Sittiflor floricola (Koch C.L., 1837) comb. n., Sitticus floricola palustris (Peckham & Peckham, 1883) = Sittiflor floricola palustris (Peckham & Peckham, 1883) comb. n., Sitticus goricus Ovtsharenko, 1978 = Attulus goricus (Ovtsharenko, 1978) comb. n., Sitticus inopinabilis Logunov, 1992 = Attulus inopinabilis (Logunov, 1992) comb. n., Sitticus inexpectus Logunov, Kronestedt, 1997 = Sittiflor inexpectus (Logunov, Kronestedt, 1997) comb. n., Sitticus juniperi Gertsch & Riechert, 1976 = Sittiab juniperi (Gertsch & Riechert, 1976) comb. n., Sitticus karakumensis Logunov, 1992 = Attulus karakumensis (Logunov, 1992) comb. n., Sitticus kazakhstanicus Logunov, 1992 = Attulus kazakhstanicus (Logunov, 1992) comb. n., Sitticus longipes (Canestrini, 1873) = Sittilong longipes (Canestrini, 1873) comb. n., Sitticus magnus Chamberlin, Ivie, 1944 = Sittiflor magnus (Chamberlin, Ivie, 1944) comb. n., Sitticus mirandus Logunov, 1993 =Attulus mirandus (Logunov, 1993) comb. n., Sitticus monstrabilis Logunov, 1992 = Sittiflor monstrabilis (Logunov, 1992), Sitticus nenilini Wesolowska, Logunov, 1993 = Attulus nenilini (Wesolowska, Logunov, 1993) comb. n., Sitticus niveosignatus (Simon, 1880) = Attulus niveosignatus (Simon, 1880) comb. n., Sitticus penicillatus (Simon, 1875) = Attulus penicillatus (Simon, 1875) comb. n., Sitticus penicilloides Wesolowska, 1981 =Attulus penicilloides (Wesolowska, 1981) comb. n., Sitticus pulchellus Logunov, 1992 = Sittiflor pulchellus (Logunov, 1992) comb. n., Sitticus ranieri (Peckham & Peckham, 1909) = Sittisax ranieri (Peckham & Peckham, 1909), Sitticus rivalis Simon, 1937 = Sittiflor striatus (Emerton, 1911) - reinstated synonym, contra Logunov, 2004 a: 35, Sitticus rupicola (Koch C.L., 1837) = Sittiflor rupicola (Koch C.L., 1837) comb. n., Sitticus saltator (Simon, 1868) = Attulus saltator (Simon, 1868) comb. n., Sitticus saxicola (C. L. Koch, 1846) = Sittisax saxicola (C. L. Koch, 1846) comb. n., Sitticus sinensis Schenkel, 1963 = Attulus sinensis (Schenkel, 1963) comb. n., Sitticus striatus Emerton, 1911 = Sittiflor striatus (Emerton, 1911) comb. n., Sitticus talgarensis Logunov & Wesolowska, 1993 = Attulus talgarensis (Logunov & Wesolowska, 1993) comb. n., Sitticus vilis (Kulczynski, 1895) =Attulus vilis (Kulczynski, 1895) comb. n., Sitticus zaisanicus Logunov, 1998 = Attulus zaisanicus (Logunov, 1998) comb. n., Sitticus zimmermanni (Simon, 1877) = Sittiflor zimmermanni (Simon, 1877).South American groups of species Sitticus leucoproctus and Sitticus palpalis are left temporarily within genus Sitticus pending further research. Pseudattulus kratochvili Caporiacco, 1955 (female only) = Sitticus cabellensis Prószyński, 1971 comb. reinstated = Sittisax cabellensis (Prószyński, 1971) comb. n.Referring to previous paper by Prószyński (2016c) I correct species synonym Myrmavola globosa (Wanless, 1978) = Toxeus globosus (Wanless, 1978), being a typing error.Also, I reconfirm hereby original genus placement of Emertonius exasperans Peckham & Peckham, 1892, as seconded by Prószyński & Deeleman-Reinhold, 2010: 164-167, figs 169-171 and documented at: http://www.peckhamia.com/salticidae/q24-Emer.html, dismissed by the World Spider Catalog, ver. 2016 with incompetent comment.Misplacement in Sitticus s.l. detected: Sitticus taiwanensis Peng X. & Li S., 2002, Sitticus wuae Peng X. & Tso I., Li S., 2002 – correction pending further research.

New portunoid fossils from southern Argentina and from the west coast of North America permit the reevaluation of the generic and family relationships within the Portunoidea Rafinesque, 1815. It has previously been suggested that the Portunidae and the Geryonidae Colosi, 1923, are closely related families (Manning and Holthuis, 1989). The new fossils suggest that the Geryonidae may in fact be derived from a portunid progenitor,ProterocarcinusFeldmann, Casadío, Chirino-Gálvez, and Aguirre Urreta, 1995, through a process of peramorphosis in which juveniles of the geryonid speciesChaceon peruvianus(d'Orbigny, 1842) resemble adults ofProterocarcinus latus(Glaessner, 1933). Examination of several genera within the portunid subfamily Polybiinae Ortmann, 1893, includingImaizumilaKarasawa, 1993;Megokkosnew genus;MinohellenusKarasawa, 1990;PororariaGlaessner, 1980;PortunitesBell, 1858; andProterocarcinus,suggests that the subfamily had an amphitropical distribution early in its history. New taxa reported here includeMegokkosnew genus andPortunites nodosusnew species. New combinations includeChaceon peruvianus(d'Orbigny, 1842),Imaizumila araucana(Philippi, 1887),Megokkos alaskensis(Rathbun, 1926),Megokkos hexagonalis(Nagao, 1932),Megokkos macrospinus(Schweitzer, Feldmann, Tucker, and Berglund, 2000),Minohellenus triangulum(Rathbun, 1926), andProterocarcinus latus(Glaessner, 1933).

This work aimed to study penA gene polymorphisms in clinical isolates of Neisseria gonorrhoeae collected in Russia in 2018–2019 and the contribution of the penA allele type to susceptibility to β-lactam antibiotics. A total of 182 isolates were analyzed. penA allele types were determined by sequencing, and the minimum inhibitory concentrations (MICs) of benzylpenicillin and ceftriaxone were measured. The influence of genetic factors on MICs was evaluated by regression analysis. All isolates were susceptible to ceftriaxone, and 40.1% of isolates were susceptible to penicillin. Eleven penA allele types were identified. The mosaic type XXXIV penA allele and the Gly120Lys substitution in PorB made the greatest contributions to increasing the ceftriaxone MIC; the presence of the blaTEM plasmid, Gly120Asp, Ala121Gly/Asn substitutions in PorB, and the adenine deletion in the promoter region of the mtrR gene caused an increase in the penicillin MIC. Among 61 NG-MAST types identified, the most frequent were types 228, 807, 9486, 1993, and 6226. A link between penA alleles and Neisseria gonorrhoeae multi-antigen sequence typing (NG-MAST) types was established. Resistance to two groups of β-lactam antibiotics was associated with non-identical changes in penA alleles. To prevent the emergence of ceftriaxone resistance in Russia, NG-MAST genotyping must be supplemented with penA allele analysis.

We redescribe Cypricercus cuneatus Sars, 1895 and Strandesia mercatorum (Vavra, 1895), type species of their genera, in order to reassess the taxonomic position of species in Cypricercus s.l. and Strandesia s.l., as well as to clarify the distinction between Cypricercus s.s. and Strandesia s.s. The morphology, taxonomy and zoogeography of these two genera are discussed. Strandesia amati (Martens, 1984) is synonymised with Strandesia lineata Victor & Fernando, 1981. Strandesia trispinosa galantis Broodbakker, 1983 becomes a synonym of the nominotypical form. Cypricercus inermis (Brady, 1904) is herewith redescribed and reinstated as a valid species, not synonymous to the type species of the genus as was previously thought. One Cypricercus (C. salinus De Deckker, 1981) and eleven Strandesia (S. crassa Klie, 1939, S. dani George & Martens, 1993, S. decorata (Sars, 1903), S. lineata Victor & Fernando, 1981, S. parva Hartmann, 1964, S. tolimensis Roessler, 1990, S. trichurensis Victor et al., 1980, S. trispinosa (Pinto & Purper, 1965), S. tuberculata Hartmann, 1964, S. umbonata Victor & Fernando, 1981, S. weberi (Moniez, 1892)) are allocated to Bradleystrandesia. Cypricercus mongolicus Daday, 1909 is transferred to Eucypris. Cypricercus xhosa sp. nov. is here described from South Africa. We also propose a conservative list of species belonging to Cypricercus s.s. and Strandesia s.s.

Paralytic shellfish toxins (PSTs) are the major neurotoxic contaminants of edible bivalves in Japan. Tetrodotoxin (TTX) was recently detected in bivalve shellfish around the world, drawing widespread attention. In Japan, high levels of TTX were reported in the digestive gland of the scallop, Patinopecten yessoensis, in 1993; however, no new data have emerged since then. In this study, we simultaneously analyzed PSTs and TTX in scallops cultured in a bay of east Japan using hydrophilic interaction chromatography (HILIC)-MS/MS. These scallops were temporally collected from April to December 2017. The highest concentration of PSTs (182 µmol/kg, total congeners) in the hepatopancreas was detected in samples collected on May 23, lined to the cell density of the dinoflagellate, Alexandrium tamarense, in seawater around the scallops, whereas the highest concentration of TTX (421 nmol/kg) was detected in samples collected on August 22. Contrary to the previous report, temporal variation of the PSTs and TTX concentrations did not coincide. The highest concentration of TTX in the entire edible tissues was 7.3 µg/kg (23 nmol/kg) in samples obtained on August 22, which was lower than the European Food Safety Authority (EFSA)-proposed threshold, 44 µg TTX equivalents/kg shellfish meat. In addition, 12β-deoxygonyautoxin 3 was firstly identified in scallops.

The louse genus Lunaceps Clay and Meinertzhagen, 1939, parasitic on shorebirds (Charadriiformes: Scolopacidae) is re-vised. Six new species and one new subspecies of Lunaceps Clay and Meinertzhagen, 1939 parasitic on shorebirds (Char-adriiformes, Scolopacidae) are described. They are L. enigmaticus sp. nov. from Stilt Sandpiper Micropalama himantopus(Bonaparte, 1826), L. kukri sp. nov. from Long-billed Curlew Numenius americanus Bechstein, 1812, L. mintoni sp. nov.from Great Knot Calidris tenuirostris (Horsfield, 1821), L. rothkoi sp. nov. from Buff-breasted Sandpiper Tryngites sub-ruficollis (Vieillot, 1819), L. schismatus sp. nov. from Dunlin Calidris alpina (Linnaeus, 1758), L. superciliosus fromSharp-tailed Sandpiper Calidris acuminata (Horsfield, 1821) and Long-toed Stint Calidris subminuta (Middendorff,1853), and L. numenii madagascariensis ssp. nov. from Far Eastern Curlew Numenius madagascariensis (Linnaeus,1766). Furthermore, the species L. cabanisi Timmermann, 1954, and L. pusillus are placed as new junior synonyms of L.incoenis (Kellogg and Chapman, 1899); the species L. haematopi Timmermann, 1954, L. oliveri Timmermann, 1954, andL. husainii Ansari, 1956, are placed as new junior synonyms of L. numenii numenii (Denny, 1842), L. numenii phaeopi(Denny, 1842), and L. falcinellus Timmermann, 1954, respectively, and the subspecies L. holophaeus timmermanniBechet, 1968, is regarded as a new junior synonym of L. falcinellus Timmermann, 1954. Lunaceps limosella limosaBechet, 1968, which was previously considered a junior synonym of L limosella Timmermann, 1954, is resurrected as avalid species. Lunaceps wilsoni Carriker, 1956, is considered a nomen dubium, and L. parabolicus Eichler (in Nietham-mer), 1953, is removed to the genus Quadraceps Clay and Meinertzhagen, 1939 as Quadraceps parabolicus comb. nov.,although its status in Quadraceps needs further attention. All species and subspecies of Lunaceps are illustrated and rede-scribed, and a key is provided for their identification. Three populations, from which only poor or limited data are available, are placed as incerta sedis.

A revision of the family Trapeziidae Miers, 1886, has shown that it consists of three clades, one of which is elevated to family status, Tetraliidae fam. nov., for the genera Tetralia Dana, 1851, and Tetraloides Galil, 1986. The genera Trapezia Latreille, 1828, Calocarcinus Calman, 1909, Hexagonalia Galil, 1986, Philippicarcinus Garth & Kim, 1983, Quadrella Dana, 1851, and Sphenomerides Rathbun, 1897, remain in the Trapeziidae; Domecia Eydoux & Souleyet, 1842, Jonesius Sankarankutty, 1962, Maldivia Borradaile, 1902, Palmyria Galil & Takeda, 1986, and the fossil genus Eomaldivia M ller & Collins, 1991, in Domeciidae Ortmann, 1893. Cladistic analysis shows that Trapeziidae sensu Miers, 1886, consists of three clades that show convergence as a result of similar habits as symbionts of reef corals and other cnidarians. A list of all recognised genera and species in the three families and their primary synonyms is provided. Keys are also included for four families of Brachyura symbiotic with reef corals, and for the genera and species of Domeciidae, Tetraliidae, and Trapeziidae. Some rare colour figures are reproduced. Three name changes have resulted within the Tetraliidae: Cancer glaberrimus Herbst, 1790, for Tetralia fulva Ser ne, 1984, and Cancer mutus Linnaeus, 1758, for Tetralia armata Dana, 1852, and Tetralia vanninii Galil & Clark, 1988. Nomenclatural problems associated with the repeated use of "forma typica" for various species of Trapezia and Tetralia are resolved. To stabilise the nomenclature of a number of well-known species, neotypes are designated for 13 species of Trapeziidae for which type material is not extant: Trapezia cymodoce (Herbst, 1801), and its three synonyms (Trapezia dentifrons Latreille, 1828, Trapezia dentata var. subintegra Dana, 1852, Trapezia cymodoce var. ornatus Chen, 1933); Trapezia bidentata (Forsk l, 1775), and one of its synonyms (Trapezia ferruginea Latreille, 1828); Trapezia digitalis Latreille, 1828, and one of its synonyms (Trapezia nigrofusca Stimpson, 1858); Trapezia septata Dana, 1852, and one of its synonyms (Trapezia reticulata Stimpson, 1858); Trapezia areolata Dana, 1852; Trapezia bella Dana, 1852; and Trapezia speciosa Dana, 1852. Neotypes are also designated for seven species of Tetraliidae: Tetralia glaberrima (Herbst, 1790), and three synonyms (Trapezia integra Latreille, 1828, Trapezia serratifrons Jacquinot, 1846, Tetralia laevissima Stimpson, 1858); Tetralia muta (Linnaeus, 1758), and one of its synonyms (Tetralia armata Dana, 1852); and Tetraloides nigrifrons (Dana, 1852).

Empirical research which aims to investigate elite sport from a holistic perspective (Magnusson & Stattin, 2006; Wylleman, 2019) is necessary to inform the ethical discussions surrounding issues such as performance and optimization. This symposium, therefore, intends to capture the complex trajectories of athlete’s lived experience from multiple angles and disciplines within the area of sport science. Starting from a psychological understanding, Philip Röthlin will introduce the prevalence of mental health disorders among Swiss elite athletes along with relevant contributing factors such as need satisfaction and organizational support. Colm Hickey will unearth how professional elite athletes are affected by abuse disguised as jokes in their daily lives from a sociological perspective. Helena Hlasová will explore retirement from elite sport through the lens of Dialogical Self Theory (Hermans & Kempen, 1993) and uncover the implicit ways in which elite athletes may or may not engage in “identity work” while transitioning out of their careers. Finally, Violetta Oblinger-Peters will present on how Olympic athletes find and create personal meaning(s) in their sport and discuss how the scientific concept translates into tangible support for athletes. Overall, the symposium intends to generate transferable knowledge of athletes’ lived reality in elite sport. References Hermans, H. J. M., & Kempen, H. J. G. (1993). The dialogical self: Meaning as movement. Academic Press. Magnusson, D., & Stattin, H. (2006). The person in context: A holistic-interactionistic approach. In W. Damon & R. M. Lerner (Eds.), Handbook of child psychology: Vol. 1. Theoretical models of human development (6th ed., pp. 400–464). Wiley. Wylleman, P., Reints, A., & De Knop, P. (2013). A developmental and holistic perspective on athletic career development. In P. Sotiriadou & V. De Bosscher (Eds.), Managing high performance sport (pp. 159–182). Routledge.