Journal articles on the topic '1842-1929'

The Afrotropical representatives of the hover fly genus Mesembrius Rondani, 1857 (Diptera) are divided into two subgenera, namely Mesembrius s.s. and Vadonimyia Séguy, 1951 and, in this present work, the subgenus Mesembrius s.s. is revised. A total of 23 Mesembrius s.s. species are recognised for the Afrotropics. Known species are re-described and six species new to science are described: Mesembrius arcuatussp. nov., M. copelandisp. nov., M. longipilosussp. nov., M. sulcussp. nov., M. tibialissp. nov. and M. vockerothisp. nov. Mesembrius africanus (Verrall, 1898) is considered a junior synonym of M. senegalensis (Macquart, 1842), M. ctenifer Hull, 1941 a junior synonym of M. caffer (Loew, 1858), M. lagopus (Loew, 1869) a junior synonym of M. capensis (Macquart, 1842) and M. platytarsis Curran, 1929 a junior synonym of M. simplicipes Curran, 1929. The females of Mesembrius chapini Curran, 1939, M. rex Curran, 1927 and M. regulus (Hull, 1937) are described for the first time. Lectotypes are designated for Mesembrius caffer, M. capensis, M. cyanipennis (Bezzi, 1915), M. minor (Bezzi, 1915), M. senegalensis, M. strigilatus (Bezzi, 1912) and M. tarsatus (Bigot, 1883). Separate identification keys for males and females are presented. We obtained 236 DNA barcodes for 18 species. The relationships amongst the different Mesembrius species are briefly discussed, based on morphological and DNA barcode data.

Opisa is a small amphipod genus including three species: O. eschrichtii (Krøyer, 1842) from the North Atlantic Ocean (Sars 1895; Bousfield 1987), the Arctic Ocean (Bousfield 1987), and the western Pacific Ocean (Stebbing 1906; Derzhavin 1929); O. odontochela Bousfield, 1987 from the southeast Alaska (Bousfield 1987); and O. tridentata Hurley, 1963 from the Pacific coasts of North America (Bousfield 1987). During field survey of the marine benthic fauna of Hokkaido, Japan, one of the authors (KK) collected an undescribed species of Opisa from off the southeast of Akkeshi Bay using a sledge net. This paper describes and illustrates the new species in detail.

This paper presents the general case study of previous works on generalized Boussinesq equations, (Abazari, 2011) and (Kılıcman and Abazari, 2012), that focuses on the application ofG′/G-expansion method with the aid of Maple to construct more general exact solutions for the coupled Boussinesq equations. In this work, the mentioned method is applied to construct more general exact solutions of Boussinesq equation and improved Boussinesq equation, which the French scientistJoseph Valentin Boussinesq(1842–1929) described in the 1870s model equations for the propagation of long waves on the surface of water with small amplitude. Our work is motivated by the fact that theG′/G-expansion method provides not only more general forms of solutions but also periodic, solitary waves and rational solutions. The method appears to be easier and faster by means of a symbolic computation.

Annette Susannah Beveridge (1842–1929) was one of the outstanding oriental scholars of the early twentieth century. The work which established her reputation is her translation of the Bābur-nāma, the autobiographical memoir of the first Mughal emperor, published in 1922 by the Royal Asiatic Society. It was the first English translation from the Chaghatai Turki in which Babur wrote his famous account. A monumental work of scholarship, it is all the more remarkable for having been completed at a time when Chaghatai language studies were in their infancy. The translation is characterized by utter reliability and precision, exhaustive footnotes and numerous appendices: Western and Asian scholars continue to consult it as the standard translation of this classic Timurid text. Yet, despite the stature of her work, little is known about Beveridge herself, an unusual figure in the British orientalist landscape if only because she was a woman who raised four children and learned oriental languages when she was past the age of 50.

On 18 March 1893 the opera Toldi by Ödön (Edmund von) Mihalovich (1842–1929) was premiered at the Royal Hungarian Opera House in Budapest. Three month later Ferenc Erkel, founder and single most important composer of the Hungarian national opera died. One of the funeral speeches at his burial was held by Mihalovich. This gesture was meant as a symbolic mounting of the guard on the national operatic scene. However, Toldi, written on a libretto based on Toldi szerelme (Toldi’s Love), the middle epic of János Arany’s Toldi trilogy, proved to be unsuccesful. It was staged again as Toldi’s Love in 1895 after a thorough revision. One cannot overlook the fact that in the newly composed third act Mihalovich wanted to write the loyalist counterpart of the conflictuous third act in Erkel’s Bánk bán. The paper discusses the question whether the first and only opera on a Hungarian text by the solid Wagnerite Mihalovich could at the time fulfil the official national expectations and become the representative national opera of the Millennium, that is, the Thousand Year Jubilee of the Carpathian Basin’s conquest by the Hungarian tribes, celebrated in 1896.

The Bornean Oxypilinae species previously included in the genus Hestiasula Saussure, 1871 are revised. External morphology and genital characters of Sundaian taxa differ considerably from the Indian type species H. brunneriana Saussure, 1871, necessitating taxonomic and nomenclatural changes. The genus Catestiasula Giglio-Tos, 1915 is reinstated. It is characterized by the apomorphic partial fusion of the dorsal and ventral laminae of the left phallomere, and by the complete reduction of the apical process. It is represented on Borneo with two species, C. nitida (Brunner de Wattenwyl, 1893) and C. moultoni Giglio-Tos, 1915. An additional species, C. seminigra (Zhang, 1992) n. comb. occurs in continental SE Asia. Two new genera are described, united by the lack of styli, the presence of dorsal carinae on the subgenital plate, and the unique morphology of the dorsal lamina of the left phallomere, but differing in the morphology of head and forelegs. Astyliasula gen. nov. accommodates A. phyllopus (De Haan, 1842) n. comb. and related species from the Sunda Islands and continental SE Asia: A. basinigra (Zhang, 1992) n. comb., A. hoffmanni (Tinkham, 1937) n. comb., A. javana (Beier, 1929) n. comb., A. major (Beier, 1929) n. comb., A. inermis (Wood-Mason, 1879) n. comb., and A. wuyshana (Yang & Wang, 1999) n. comb.. Hestias sarawaca Westwood, 1889 is removed from synonymy with A. phyllopus and reinstated as A. sarawaca (Westwood, 1889) n. comb.. The monotypic taxon Pseudohestiasula borneana gen. nov. sp. nov. is erected for a Bornean endemic more closely related to Astyliasula than to the other genera. Hestiasula is now restricted to H. brunneriana and related species from India and adjacent countries. The tribe Hestiasulini Giglio-Tos, 1915 stat. rev. is proposed for all genera more closely related to Hestiasula than to other Oxypilinae, that is Hestiasula, Ephestiasula, Catestiasula, Astyliasula, and Pseudohestiasula. New data on the ecology and distribution of all Bornean Hestiasulini as well as a key to the Oxypilinae of Borneo are provided.

Afrotropical species of the Craspedophorus leprieuri and Craspedophorus regalis groups are revised. C. clasispilus (Alluaud, 1915) and C. guineensis Basilewsky, 1987 are considered as subspecies of C. leprieuri (Laporte de Castelnau, 1835); the synonymized C. peringueyi Csiki, 1929 (=laticollis Péringuey, 1904) is restated as subspecies of C. leprieuri, and it is described C. leprieuri zambianus (DR Congo: Katanga Province; Zambia); C. pseudofestivus Burgeon, 1930 is considered subspecies of C. merus Péringuey, 1904, and it is described C. merus lundanus (Angola, DR Congo: Kasai-Oriental and Katanga Provinces); C. bouvieri imperialis Burgeon, 1930 is considered to be a separate species of C. bouvieri (Rousseau, 1905), and C. bouvieri dux Basilewsky, 1951 is transferred to C. imperialis. The synonymized C. sayersii (Hope, 1842) is considered to be a good subspecies of C. regalis. C. bouvieri crampeli (Alluaud, 1915) is removed from C. bouvieri, and transferred to C. reflexus (Fabricius, 1781) in the C. reflexus species group (Häckel 2016). In this group C. uelensis Burgeon, 1930 is considered to be a subspecies of C. reflexus; and C. bozasi Alluaud, 1930 is synonymized with C. reflexus uelensis Burgeon, 1930. C. arnosti Häckel 2016 is synonymized with C. reflexus crampeli (Alluaud, 1915), C. ethmoides Alluaud, 1930 is synonymized with C. impictus (Boheman, 1848), and C. lebaudyi Alluaud, 1932 is synonymized with C. stanleyi Alluaud, 1930.

Faltam estudos sobre as relações entre os Bispos católicos no Brasil em que fiquem demonstradas as práticas intersubjetivas de atuação enquanto grupo, os esforços coletivos de busca de consenso, como também diferenças, rivalidades, tensões e até conflitos. Este artigo analisa o conflito teológico-político entre o Arcebispo-Primaz, Dom Romualdo Antônio de Seixas (1787-1860), e o Bispo do Rio de Janeiro e Capelão-Mor da Casa Imperial, Dom Manoel do Monte Rodrigues de Araújo (1796-1863), pelo direito e privilégio de sagrar e coroar o jovem Dom Pedro II, em julho de 1841. Os dois bispos deixaram duas longas publicações, “Opúsculo sobre a questão que tivera o Excellentíssimo Arcebispo da Bahia e Metropolitano do Brasil D. Romualdo Antônio de Seixas, com o Bispo Capellão-Mór do Rio de Janeiro Manoel do Monte Rodrigues de Araújo...” (1841) de Dom Manoel do Monte, e “Memória apologética do Arcebispo da Bahia, Metropolitano e Primaz do Brasil, em resposta à um Opúsculo...” (1842) de Dom Romualdo de Seixas, em que relatam os fatos, a partir da ótica de cada um, e os argumentos jurídico-canônicos em defesa de suas posições. Para análise do caso optamos seguir o paradigma intersubjetivo proposto por Jürgen Habermas (1929) que está em ação no diálogo, na comunicação, na interação, especialmente, em situações de “conflitos moralmente relevantes”. A divergência intensa entre os dois Prelados revelou o grande distanciamento entre os bispos brasileiros e que nos remete para o problema do exercício de uma “colegialidade episcopal”.

An investigation of ecto- and endoparasites of wild rabbit Oryctolagus cuniculus (L., 1758) was made during February and March 2004. Together five species of ectoparasites and seven species of endopara- sites was found in five specimens of host. Ectoparasites: acarids Leporacarus gibbus (Pagenstecher, 1862), Psoroptes cuniculi (Delafond, 1859), and Cheyletiella parasitivorax (Mégnin, 1878), flea Spilopsyllus cuniculi (Dale, 1878), and louse Haemodipsus ventricosus (Denny, 1842). Except of petechial haemorrhagies inside both earlobes of one rabbit neither hyperkeratosis nor scale with any degrees of hairlessness were detected. Higher incidence of flea Spilopsyllus cuniculi could be important for spreading of myxomatosis. In one rabbit abnormal damage of incisivi was found, which caused the highest documented incidence of acarids Cheyletiella parasitivorax (485 ex.), fleas Spilopsyllus cuniculi (65 ex.), and especially enormous amount of louse Haemodipsus ventricosus (1840 ex). This finding establish close relation between prevalence and counts of ectoparasites with health of host, because popu- lation of ectoparasites from different taxonomic groups are principally affected by effective hostęs cleanup. Handicapped hosts are not able to make clarify as effective as the healthy ones. Endoparasites: tapeworm Taenia pisiformis (Bloch, 1780) – larvae, nematods Passalurus ambiguus (Rudolphi, 1819) Rudolphi, 1845; Graphidium strigosum (Dujardin, 1845) Railliet and Henry, 1909, Trichostrongylus retortaeformis (Zeder, 1800) Loos, 1905 and protozoa Eimeria piriformis Kotlan & Pospesch, 1934; E. media Kessel, 1929, and E. perforans (Leuckart, 1879) Sluiter & Swellengrebel, 1912. All endoparasites were found in very low or middle intensity, which does not seem to be main cause of decreasing number of wild rabbits in monitored areas.

The entomological collection of László börzsöny was donated to the rippl-rónai museum (Kaposvár) in 2019. Osmylidae 2 exx. - 2 sp., mantispidae 1 ex. - 1 sp., hemerobii-dae 2 exx. - 1 sp., Chrysopidae 28 exx. - 12 sp., nemopteridae 100 exx. - 6 sp., myrmeleontidae: ascalaphinae 444 exx. - 68 sp. were identified in this collection. During the identification, 3 new synonyms were revealed namely Palparidius fascipennis(banks, 1911) (syn. n.) a new junior synonym of Palparidius capicolaPéringuey, 1910, Ululodes sinuatus banks, 1924 (syn. n.) a new junior synonym of Cordulecerus praecellens (Gers-taecker, 1885), Agrionosoma pendleburyi Fraser, 1927 (syn. n.) is a new junior synonym of Agrionosoma dohrni van der Weele, 1909. the lectotype of Suphalomitus buyssoni van der Weele, 1909 and the lectotype of Suhpalacsa donckieri navás, 1913 were designated. Several species were found as new records for the local faunas: Dielocroce chobauti (mclachlan, 1898) for Jordan; Ameropterus selysi (van der Weele, 1909) for Peru and French Guiana; Cordulecerus praecellens (Ger-staecker, 1885), Amoea arenosa (Walker, 1853) Haploglenius cuboides Jones sl. and Ululodes venezolensis van der Weele, 1909 (stat. n.) for Peru; Allocormodes junodi van der Weele, 1909 for tanzania; Ascalobyas microcerus (rambur, 1842) for belize; Protidricerus elwesii (mcLachlan, 1891) for myanmar, thailand and vietnam; Tmesibasis rothschildi van der Weele, 1907 for ethiopia; Agrionosoma dohrni van der Weele, 1909 and Agrionosoma swinhoei van der Weele, 1909 for myanmar; Encyoposis seydeli (navás, 1929) for Zambia; Glyptobasis cor-nuta Kimmins, 1949 for nepal; Libelloides sibiricus (eversmann, 1850) for mongolia; Maezous tomijankae Ábrahám, 2008 for China and vietnam; Malesianus harisi (Ábrahám, 2008) for Indonesia; Nephoneura costalis van der Weele, 1909 for Zam-bia, Ghana, Cameroon; Phalascusa vassei van der Weele, 1909 for Kenya. Zambia, namibia and Suphalomitus formosanusEsben-Petersen, 1913 for Vietnam.

Changes to the treatment of Coleoptera family-group names published by Bouchard et al. (2011) are given. These include necessary additions and corrections based on much-appreciated suggestions from our colleagues, as well as our own research. Our ultimate goal is to assemble a complete list of available Coleoptera family-group names published up to the end of 2010 (including information about their spelling, author, year of publication, and type genus). The following 59 available Coleoptera family-group names are based on type genera not included in Bouchard et al. (2011): Prothydrinae Guignot, 1954, Aulonogyrini Ochs, 1953 (Gyrinidae); Pogonostomini Mandl 1954, Merismoderini Wasmann, 1929, †Escheriidae Kolbe, 1880 (Carabidae); Timarchopsinae Wang, Ponomarenko & Zhang, 2010 (Coptoclavidae); Stictocraniini Jakobson, 1914 (Staphylinidae); Cylindrocaulini Zang, 1905, Kaupiolinae Zang, 1905 (Passalidae); Phaeochroinae Kolbe, 1912 (Hybosoridae); Anthypnidae Chalande, 1884 (Glaphyridae); Comophorini Britton, 1957, Comophini Britton, 1978, Chasmidae Streubel, 1846, Mimelidae Theobald, 1882, Rhepsimidae Streubel, 1846, Ometidae Streubel, 1846, Jumnidae Burmeister, 1842, Evambateidae Gistel, 1856 (Scarabaeidae); Protelmidae Jeannel, 1950 (Byrrhoidea); Pseudeucinetini Csiki, 1924 (Limnichidae); Xylotrogidae Schönfeldt, 1887 (Bostrichidae); †Mesernobiinae Engel, 2010, Fabrasiinae Lawrence & Reichardt, 1966 (Ptinidae); Arhinopini Kirejtshuk & Bouchard, 2018 (Nitidulidae); Hypodacninae Dajoz, 1976, Ceuthocera Mannerheim, 1852 (Cerylonidae); Symbiotinae Joy, 1932 (Endomychidae); Cheilomenini Schilder & Schilder, 1928, Veraniini Schilder & Schilder, 1928 (Coccinellidae); Ennearthroninae Chûjô, 1939 (Ciidae); Curtimordini Odnosum, 2010, Mordellochroini Odnosum, 2010 (Mordellidae); Chanopterinae Borchmann, 1915 (Promecheilidae); Heptaphyllini Prudhomme de Borre, 1886, Olocratarii Baudi di Selve, 1875, Opatrinaires Mulsant & Rey, 1853, Telacianae Poey, 1854, Ancylopominae Pascoe, 1871 (Tenebrionidae); Oxycopiini Arnett, 1984 (Oedemeridae); Eutrypteidae Gistel, 1856 (Mycteridae); Pogonocerinae Iablokoff-Khnzorian, 1985 (Pyrochroidae); Amblyderini Desbrochers des Loges, 1899 (Anthicidae); Trotommideini Pic, 1903 (Scraptiidae); Acmaeopsini Della Beffa, 1915, Trigonarthrini Villiers, 1984, Eunidiini Téocchi, Sudre & Jiroux, 2010 (Cerambycidae); Macropleini Lopatin, 1977, Stenopodiides Horn, 1883, Microrhopalides Horn, 1883, Colaphidae Siegel, 1866, Lexiphanini Wilcox, 1954 (Chrysomelidae); †Medmetrioxenoidesini Legalov, 2010, †Megametrioxenoidesini Legalov, 2010 (Nemonychidae); Myrmecinae Tanner, 1966, Tapinotinae Joy, 1932, Acallinae Joy, 1932, Cycloderini Hoffmann, 1950, Sthereini Hatch, 1971 (Curculionidae). The following 21 family-group names, listed as unavailable in Bouchard et al. (2011), are determined to be available: Eohomopterinae Wasmann, 1929 (Carabidae); Prosopocoilini Benesh, 1960, Pseudodorcini Benesh, 1960, Rhyssonotini Benesh, 1960 (Lucanidae); Galbini Beaulieu, 1919 (Eucnemidae); Troglopates Mulsant & Rey, 1867 (Melyridae); Hippodamiini Weise, 1885 (Coccinellidae); Micrositates Mulsant & Rey, 1854, Héliopathaires Mulsant & Rey, 1854 (Tenebrionidae); Hypasclerini Arnett, 1984; Oxaciini Arnett, 1984 (Oedemeridae); Stilpnonotinae Borchmann, 1936 (Mycteridae); Trogocryptinae Lawrence, 1991 (Salpingidae); Grammopterini Della Beffa, 1915, Aedilinae Perrier, 1893, Anaesthetinae Perrier, 1893 (Cerambycidae); Physonotitae Spaeth, 1942, Octotomides Horn, 1883 (Chrysomelidae); Sympiezopinorum Faust, 1886, Sueinae Murayama, 1959, Eccoptopterini Kalshoven, 1959 (Curculionidae). The following names were proposed as new without reference to family-group names based on the same type genus which had been made available at an earlier date: Dineutini Ochs, 1926 (Gyrinidae); Odonteini Shokhin, 2007 (Geotrupidae); Fornaxini Cobos, 1965 (Eucnemidae); Auletobiina Legalov, 2001 (Attelabidae). The priority of several family-group names, listed as valid in Bouchard et al. (2011), is affected by recent bibliographic discoveries or new nomenclatural interpretations. †Necronectinae Ponomarenko, 1977 is treated as permanently invalid and replaced with †Timarchopsinae Wang, Ponomarenko & Zhang, 2010 (Coptoclavidae); Agathidiini Westwood, 1838 is replaced by the older name Anisotomini Horaninow, 1834 (Staphylinidae); Cyrtoscydmini Schaufuss, 1889 is replaced by the older name Stenichnini Fauvel, 1885 (Staphylinidae); Eremazinae Iablokoff-Khnzorian, 1977 is treated as unavailable and replaced with Eremazinae Stebnicka, 1977 (Scarabaeidae); Coryphocerina Burmeister, 1842 is replaced by the older name Rhomborhinina Westwood, 1842 (Scarabaeidae); Eudysantina Bouchard, Lawrence, Davies & Newton, 2005 is replaced by the older name Dysantina Gebien, 1922 which is not permanently invalid (Tenebrionidae). The names Macraulacinae/-ini Fleutiaux, 1923 (Eucnemidae), Anamorphinae Strohecker, 1953 (Endomychidae), Pachycnemina Laporte, 1840 (Scarabaeidae), Thaumastodinae Champion, 1924 (Limnichidae), Eudicronychinae Girard, 1971 (Elateridae), Trogoxylini Lesne, 1921 (Bostrichidae), Laemophloeidae Ganglbauer, 1899 (Laemophloeidae); Ancitini Aurivillius, 1917 (Cerambycidae) and Tropiphorini Marseul, 1863 (Curculionidae) are threatened by the discovery of older names; Reversal of Precedence (ICZN 1999: Art. 23.9) or an application to the International Commission on Zoological Nomenclature will be necessary to retain usage of the younger synonyms. Reversal of Precedence is used herein to qualify the following family-group names as nomina protecta: Murmidiinae Jacquelin du Val, 1858 (Cerylonidae) and Chalepini Weise, 1910 (Chrysomelidae). The following 17 Coleoptera family-group names (some of which are used as valid) are homonyms of other family-group names in zoology, these cases must be referred to the Commission for a ruling to remove the homonymy: Catiniidae Ponomarenko, 1968 (Catiniidae); Homopterinae Wasmann, 1920, Glyptini Horn, 1881 (Carabidae); Tychini Raffray, 1904, Ocypodina Hatch, 1957 (Staphylinidae); Gonatinae Kuwert, 1891 (Passalidae); Aplonychidae Burmeister, 1855 (Scarabaeidae); Microchaetini Paulus, 1973 (Byrrhidae); Epiphanini Muona, 1993 (Eucnemidae); Limoniina Jakobson, 1913 (Elateridae); Ichthyurini Champion, 1915 (Cantharidae); Decamerinae Crowson, 1964 (Trogossitidae); Trichodidae Streubel, 1839 (Cleridae); Monocorynini Miyatake, 1988 (Coccinellidae); Gastrophysina Kippenberg, 2010, Chorinini Weise, 1923 (Chrysomelidae); Meconemini Pierce, 1930 (Anthribidae). The following new substitute names are proposed: Phoroschizus (to replace Schizophorus Ponomarenko, 1968) and Phoroschizidae (to replace Schizophoridae Ponomarenko, 1968); Mesostyloides (to replace Mesostylus Faust, 1894) and Mesostyloidini (to replace Mesostylini Reitter, 1913). The following new genus-group name synonyms are proposed [valid names in square brackets]: Plocastes Gistel, 1856 [Aesalus Fabricius, 1801] (Lucanidae); Evambates Gistel, 1856 [Trichius Fabricius, 1775] (Scarabaeidae); Homoeoplastus Gistel, 1856 [Byturus Latreille, 1797] (Byturidae). Two type genera previously treated as preoccupied and invalid, Heteroscelis Latreille, 1828 and Dysantes Pascoe, 1869 (Tenebrionidae), are determined to be senior homonyms based on bibliographical research. While Dysantes is treated as valid here, Reversal of Precedence (ICZN 1999: Art. 23.9) is used to conserve usage of Anomalipus Guérin-Méneville, 1831 over Heteroscelis.

The university in Vilna (Lithuanian: Vilnius), now Vilniaus universitetas, founded in 1579 by Stefan Batory (Stephen Báthory), King of Poland and Grand Duke of Lithuania, was a centre of Polish botany in 1780-1832 and 1919-1939. The Botanic Garden established by Jean-Emmanuel Gilibert (1741–1814) in 1781 (or, actually, from 1782) survived the loss of independence by Poland (1795), and a later closure of the University (1832), and it continued to function until 1842, when it was shut down by Russian authorities. After Poland had regained independence and the University was reopened as the Stefan Batory University (SBU), its Botanic Garden was established on a new location (1919, active since 1920). It survived as a Polish institution until 1939. After the Second World War, as a result of changed borders, it found itself in the Soviet Union, and from 1990 – in the Republic of Lithuania. A multidisciplinary research project has been recently launched with the aim to create a publication on the history of science at the Stefan Batory University. The botanical part of the project includes, among others, drafting the history of the Botanic Garden. Obtaining electronic copies of archival documents, e.g. annual reports written by the directors, enabled a more thorough analysis of the Garden’s history. Piotr Wiśniewski (1884–1971), a plant physiologist, nominated as Professor in the Department of General Botany on 1 June 1920, was the organiser and the first director of the Garden. He resigned from his post in October 1923, due to financial problems of the Garden. From October 1923 to April 1924, the management was run by the acting director, Edward Bekier (1883–1945), Professor in the Department of Physical Chemistry, Dean of the Faculty of Mathematics and Natural Sciences. For 13 subsequent years, i.e. from 1 May 1924 to 30 April 1937, the directorship of the Garden was held by Józef Trzebiński (1867–1941), a mycologist and one of the pioneers of phytopathology in Poland, Head of the Department of Botany II (Agricultural Botany), renamed in 1926 as the Department of Plant Taxonomy, and in 1937 – the Department of Taxonomy and Geography of Plants. From May 1937 to 1939, his successor as director was Franciszek Ksawery Skupieński (1888–1962), a researcher of slime moulds. Great credit for the development of the Garden is due to the Inspector, i.e. Chief Gardener, Konstanty Prószyński (Proszyński) (1859–1936) working there from 1919, through his official nomination in 1920, until his death. He was an amateur-naturalist, a former landowner, who had lost his property. Apart from the work on establishing and maintaining the Garden’s collection, as well as readying seeds for exchange, he published one mycological paper, and prepared a manuscript on fungi, illustrated by himself, containing descriptions of the new species. Unfortunately, this work was not published for lack of funds, and the prepared material was scattered. Some other illustrations of flowering plants drawn by Prószyński survived. There were some obstacles to the further development of the institution, namely substantially inadequate funds as well as too few members of the personnel (1–3 gardeners, and 1–3 seasonal workers). The area of the Garden, covering approx. 2 hectares was situated on the left bank of the Neris river (Polish: Wilia). It was located on sandy soils of a floodplain, and thus liable to flooding. These were the reasons for the decision taken in June 1939 to move the Garden to a new site but the outbreak of the Second World War stood in the way. Despite these disadvantageous conditions, the management succeeded in setting up sections of plants analogous to these established in other botanical gardens in Poland and throughout the world, i.e. general taxonomy (1922), native flora (1922), psammophilous plants (1922), cultivated plants (1924/1925), plant ecology (1927/1928), alpinarium (1927–1929), high-bog plants (1927–1929), and, additionally – in the 1920s – the arboretum, as well as sections of aquatic and bog plants. A glasshouse was erected in 1926–1929 to provide room for plants of warm and tropical zones. The groups representing the various types of vegetation illustrated the progress in ecology and phytosociology in the science of the period (e.g. in the ecology section, the Raunkiaer’s life forms were presented). The number of species grown increased over time, from 1,347 in 1923/1924 to approx. 2,800 in 1936/1937. Difficult weather conditions – the severe winter of 1928 as well as the snowless winter and the dry summer of 1933/34 contributed to the reduction of the collections. The ground collections, destroyed by flood in spring of 1931, were restored in subsequent years. Initially, the source of plant material was the wild plant species collected during field trips. Many specimens were also obtained from other botanical gardens, such as Warsaw and Cracow (Kraków). Beginning from 1923, printed catalogues of seeds offered for exchange were published (cf. the list on p. ... ). Owing to that, the Garden began to participate in the national and international plant exchange networks. From its inception, the collection of the Garden was used for teaching purposes, primarily to the students of the University, as well as for the botanical education of schoolchildren and the general public, particularly of the residents of Vilna. Scientific experiments on phytopathology were conducted on the Garden’s plots. After Vilna was incorporated into Lithuania in October 1939, the Lithuanian authorities shut down the Stefan Batory University, thus ending the history of the Polish Botanic Garden. Its area is now one of the sections of the Vilnius University Botanic Garden (“Vingis” section – Vilniaus universiteto botanikos sodas). In 1964, its area was extended to 7.35 hectares. In 1974, after establishing the new Botanic Garden in Kairenai to the east of Vilnius, the old Garden lost its significance. Nevertheless, it still serves the students and townspeople of Vilnius, and its collections of flowering plants are often used to decorate and grace the university halls during celebrations.

The genus Olios Walckenaer, 1837 is revised, a generic diagnosis is given and an identification key to eight species groups is provided. Olios in its revised sense includes 87 species and is distributed in Africa, southern Europe and Asia. Three species groups are revised in this first part, an identification key to species for each group is provided, five new species are described and all included species are illustrated. The Olios argelasius-group includes O. argelasius Walckenaer, 1806, O. canariensis (Lucas, 1838), O. pictus (Simon, 1885), O. fasciculatus Simon, 1880 and O. kunzi spec. nov. (male, female; Namibia, Zambia, South Africa); it is distributed in the Mediterranean region, northern Africa including Canary Islands, in the Middle East, South Sudan, East Africa, and southern Africa. The Olios coenobitus-group includes O. angolensis spec. nov. (male; Angola), O. coenobitus Fage, 1926, O. denticulus spec. nov. (male; Java), O. erraticus Fage, 1926, O. gambiensis spec. nov. (male, female; Gambia), O. milleti (Pocock, 1901b), O. mordax (O. Pickard-Cambridge, 1899) and O. pusillus Simon, 1880; it is distributed in Africa (Gambia, Angola, Tanzania, Madagascar) and Asia (India, Sri Lanka, Indonesia: Java). The Olios auricomis-group includes only O. auricomis (Simon, 1880), distributed in Africa south of 10°N. Other species groups are introduced briefly and will be revised in forthcoming revisions. The Olios correvoni-group includes currently O. claviger (Pocock, 1901a), O. correvoni Lessert, 1921, O. correvoni choupangensis Lessert, 1936, O. darlingi (Pocock, 1901a), O. faesi Lessert, 1933, O. freyi Lessert, 1929, O. kassenjicola Strand, 1916b, O. kruegeri (Simon, 1897a), O. quadrispilotus (Simon, 1880) comb. nov., O. lucieni comb. nov. nom. nov., O. sjostedti Lessert, 1921 and O. triarmatus Lessert, 1936; it is distributed in Africa (Zimbabwe, Tanzania incl. Zanzibar, Angola, Congo, Central Africa, South Africa, Botswana; O. darlingi was recorded from Zimbabwe and Botswana and not from South Africa). The Olios rossettii-group includes: O. baulnyi (Simon, 1874), O. bhattacharjeei (Saha & Raychaudhuri, 2007), O. brachycephalus Lawrence, 1938, O. floweri Lessert, 1921, O. jaldaparaensis Saha & Raychaudhuri, 2007, O. japonicus Jäger & Ono, 2000, O. kolosvaryi (Caporiacco, 1947b) comb. nov., O. longipes (Simon, 1884b), O. lutescens (Thorell, 1894), O. mahabangkawitus Barrion & Litsinger, 1995, O. obesulus (Pocock, 1901b), O. rossettii (Leardi, 1901), O. rotundiceps (Pocock, 1901b), O. sericeus (Kroneberg, 1875), O. sherwoodi Lessert, 1929, O. suavis (O. Pickard-Cambridge, 1876), O. tarandus (Simon, 1897d), O. tener (Thorell, 1891) and O. tiantongensis (Zhang & Kim, 1996); it is distributed in the Mediterranean region, in Africa (especially eastern half) and Asia (Middle East and Central Asia to Japan, Philippines and Java). The Olios nentwigi-group includes O. diao Jäger, 2012, O. digitatus Sun, Li & Zhang, 2011, O. jaenicke Jäger, 2012, O. muang Jäger, 2012, O. nanningensis (Hu & Ru, 1988), O. nentwigi spec. nov. (male, female; Indonesia: Krakatau), O. perezi Barrion & Litsinger, 1995, O. scalptor Jäger & Ono, 2001 and O. suung Jäger, 2012; it is distributed in Asia (Thailand, Laos, Vietnam, Cambodia, China, Taiwan, Indonesia, Philippines), Papua New Guinea and Mariana Islands. Olios diao is newly recorded from Cambodia and Champasak Province in Laos. The Olios stimulator-group includes O. admiratus (Pocock, 1901b), O. hampsoni (Pocock, 1901b), O. lamarcki (Latreille, 1806) and O. stimulator Simon, 1897c; it is distributed in Africa (Madagascar, Seychelles), Middle East and South Asia (United Arab Emirates, Iraq, Afghanistan, Pakistan, India, Maldives, Sri Lanka). The Olios hirtus-group includes O. bungarensis Strand, 1913b, O. debalae (Biswas & Roy, 2005), O. ferox (Thorell, 1892), O. hirtus (Karsch, 1879a), O. igraya (Barrion & Litsinger, 1995) comb. nov., O. menghaiensis (Wang & Zhang, 1990), O. nigrifrons (Simon, 1897b), O. punctipes Simon, 1884a, O. punctipes sordidatus (Thorell, 1895), O. pyrozonis (Pocock, 1901b), O. sungaya (Barrion & Litsinger, 1995) comb. nov., O. taprobanicus Strand, 1913b and O. tikaderi Kundu et al., 1999; it is distributed in South, East and Southeast Asia (Sri Lanka, India, Nepal, Bangladesh, Myanmar, China, Laos, Thailand, Cambodia, Vietnam, Malaysia, Indonesia, Philippines). Nineteen synonyms are recognised: Nisueta Simon, 1880, Nonianus Simon, 1885, both = Olios syn. nov.; O. spenceri Pocock, 1896, O. werneri (Simon, 1906a), O. albertius Strand, 1913a, O. banananus Strand, 1916a, O. aristophanei Lessert, 1936, all = O. fasciculatus; O. subpusillus Strand, 1907c = O. pusillus; O. schonlandi (Pocock, 1900b), O. rufilatus Pocock, 1900c, O. chiracanthiformis Strand, 1906, O. ituricus Strand, 1913a, O. isongonis Strand, 1915, O. flavescens Caporiacco, 1941 comb. nov., O. pacifer Lessert, 1921, all = O. auricomis; Olios sanguinifrons (Simon, 1906b) = O. rossettii Leardi, 1901; O. phipsoni (Pocock, 1899), Sparassus iranii (Pocock, 1901b), both = O. stimulator; O. fuligineus (Pocock, 1901b) = O. hampsoni. Nine species are transferred to Olios: O. gaujoni (Simon, 1897b) comb. nov., O. pictus comb. nov., O. unilateralis (Strand, 1908b) comb. nov. (all three from Nonianus), O. affinis (Strand, 1906) comb. nov., O. flavescens Caporiacco, 1941 comb. nov., O. quadrispilotus comb. nov., O. similis (Berland, 1922) comb. nov. (all four from Nisueta), O. sungaya (Barrion & Litsinger, 1995) comb. nov., O. igraya (Barrion & Litsinger, 1995) comb. nov. (both from Isopeda L. Koch 1875). Olios lucieni nom. nov. comb. nov. is proposed for Nisueta similis Berland, 1922, which becomes a secondary homonym. The male of O. quadrispilotus comb. nov. is described for the first time. Sixteen species are currently without affiliation to one of the eight species groups: O. acolastus (Thorell, 1890), O. alluaudi Simon, 1887a, O. batesi (Pocock, 1900c), O. bhavnagarensis Sethi & Tikader, 1988, O. croseiceps (Pocock, 1898b), O. durlaviae Biswas & Raychaudhuri, 2005, O. gentilis (Karsch, 1879b), O. gravelyi Sethi & Tikader, 1988, O. greeni (Pocock, 1901b), O. inaequipes (Simon 1890), O. punjabensis Dyal, 1935, O. ruwenzoricus Strand, 1913a, O. senilis Simon, 1880, O. somalicus Caporiacco, 1940, O. wroughtoni (Simon, 1897c) and O. zulu Simon, 1880. Five of these species are illustrated in order to allow identification of the opposite (male) sex and to settle their systematic placement. Thirty-seven species are considered nomina dubia, mostly because they were described from immatures, three of them are illustrated: O. abnormis (Blackwall, 1866), O. affinis (Strand, 1906) comb. nov., O. africanus (Karsch, 1878), O. amanensis Strand, 1907a, O. annandalei (Simon, 1901), O. bivittatus Roewer, 1951, O. ceylonicus (Leardi, 1902), O. conspersipes (Thorell, 1899), Palystes derasus (C.L. Koch, 1845) comb. nov., O. detritus (C.L. Koch, 1845), O. digitalis Eydoux & Souleyet, 1842, O. exterritorialis Strand, 1907b, O. flavovittatus (Caporiacco, 1935), O. fugax (O. Pickard-Cambridge, 1885), O. guineibius Strand, 1911c, O. guttipes (Simon, 1897a), O. kiranae Sethi & Tikader, 1988, O. longespinus Caporiacco, 1947b, O. maculinotatus Strand, 1909, O. morbillosus (MacLeay, 1827), O. occidentalis (Karsch, 1879b), O. ornatus (Thorell, 1877), O. pagurus Walckenaer, 1837, O. patagiatus (Simon, 1897b), O. praecinctus (L. Koch, 1865), O. provocator Walckenaer, 1837, O. quesitio Moradmand, 2013, O. quinquelineatus Taczanowski, 1872, O. sexpunctatus Caporiacco, 1947a, Heteropoda similaris (Rainbow, 1898) comb. rev., O. socotranus (Pocock, 1903), O. striatus (Blackwall, 1867), O. timidus (O. Pickard-Cambridge, 1885), Remmius variatus (Thorell, 1899) comb. nov., O. vittifemur Strand, 1916b, O. wolfi Strand, 1911a and O. zebra (Thorell, 1881). Eighty-nine species are misplaced in Olios but cannot be affiliated to any of the known genera. They belong to the subfamilies Deleninae Hogg, 1903, Sparassinae Bertkau, 1872 and Palystinae Simon, 1897a, nineteen of them are illustrated: O. acostae Schenkel, 1953, O. actaeon (Pocock, 1898c), O. artemis Hogg, 1915, O. atomarius Simon, 1880, O. attractus Petrunkevitch, 1911, O. auranticus Mello-Leitão, 1918, O. benitensis (Pocock, 1900c), O. berlandi Roewer, 1951, O. biarmatus Lessert, 1925, O. canalae Berland, 1924, O. caprinus Mello-Leitão, 1918, O. chelifer Lawrence, 1937, O. chubbi Lessert, 1923, O. clarus (Keyserling, 1880), O. coccineiventris (Simon, 1880), O. corallinus Schmidt, 1971, O. crassus Banks, 1909, O. debilipes Mello-Leitão, 1945, O. discolorichelis Caporiacco, 1947a, O. erroneus O. Pickard-Cambridge, 1890, O. extensus Berland, 1924, O. fasciiventris Simon, 1880 , O. feldmanni Strand, 1915, O. fimbriatus Chrysanthus, 1965, O. flavens Nicolet, 1849, O. fonticola (Pocock, 1902), O. formosus Banks, 1929, O. francoisi (Simon, 1898a), O. fulvithorax Berland, 1924, O. galapagoensis Banks, 1902, O. gaujoni (Simon, 1897b) comb. nov., O. giganteus Keyserling, 1884, O. hoplites Caporiacco, 1941, O. humboldtianus Berland, 1924, O. insignifer Chrysanthus, 1965, O. insulanus (Thorell, 1881), O. keyserlingi (Simon, 1880), O. lacticolor Lawrence, 1952, O. lepidus Vellard, 1924, O. longipedatus Roewer, 1951, O. machadoi Lawrence, 1952, O. macroepigynus Soares, 1944, O. maculatus Blackwall, 1862, O. marshalli (Pocock, 1898a), O. mathani (Simon, 1880), O. minensis Mello-Leitão, 1917, O. monticola Berland, 1924, O. mutabilis Mello-Leitão, 1917, O. mygalinus Doleschall, 1857, O. mygalinus cinctipes Merian, 1911, O. mygalinus nirgripalpis Merian, 1911, O. neocaledonicus Berland, 1924, O. nigristernis (Simon, 1880), O. nigriventris Taczanowski, 1872, O. oberzelleri Kritscher, 1966, O. obscurus (Keyserling, 1880), O. obtusus F.O. Pickard-Cambridge, 1900, O. orchiticus Mello-Leitão, 1930, O. oubatchensis Berland, 1924, O. paraensis (Keyserling, 1880), O. pellucidus (Keyserling, 1880), O. peruvianus Roewer, 1951, O. pictitarsis Simon, 1880, O. plumipes Mello-Leitão, 1937, O. princeps Hogg, 1914, O. pulchripes (Thorell, 1899), O. puniceus (Simon, 1880), O. roeweri Caporiacco, 1955a, O. rubripes Taczanowski, 1872, O. rubriventris (Thorell, 1881), O. rufus Keyserling, 1880, O. sanctivincenti (Simon, 1898b), O. similis (O. Pickard-Cambridge, 1890), O. simoni (O. Pickard-Cambridge, 1890), O. skwarrae Roewer, 1933, O. spinipalpis (Pocock, 1901a), O. stictopus (Pocock, 1898a), O. strandi Kolosváry, 1934, O. subadultus Mello-Leitão, 1930, O. sulphuratus (Thorell, 1899), O. sylvaticus (Blackwall, 1862), O. tamerlani Roewer, 1951, O. tigrinus (Keyserling, 1880), O. trifurcatus (Pocock, 1900c), O. trinitatis Strand, 1916a, O. velox (Simon, 1880), O. ventrosus Nicolet, 1849, O. vitiosus Vellard, 1924 and O. yucatanus Chamberlin, 1925. Seventeen taxa are transferred from Olios to other genera within Sparassidae, eight of them are illustrated: Adcatomus luteus (Keyserling, 1880) comb. nov., Eusparassus flavidus (O. Pickard-Cambridge, 1885) comb. nov., Palystes derasus (C.L. Koch, 1845) comb. nov., Heteropoda similaris (Rainbow, 1898) comb. rev., Remmius variatus (Thorell, 1899) comb. nov., Nolavia audax (Banks, 1909) comb. nov., Nolavia antiguensis (Keyserling, 1880) comb. nov., Nolavia antiguensis columbiensis (Schmidt, 1971) comb. nov., Nolavia fuhrmanni (Strand, 1914) comb. nov., Nolavia helva (Keyserling, 1880) comb. nov., Nolavia stylifer (F.O. Pickard-Cambridge, 1900) comb. nov., Nolavia valenciae (Strand, 1916a) comb. nov., Nungara cayana (Taczanowski, 1872) comb. nov., Polybetes bombilius (F.O. Pickard-Cambridge, 1899) comb. nov., Polybetes fasciatus (Keyserling, 1880) comb. nov., Polybetes hyeroglyphicus (Mello-Leitão, 1918) comb. nov. and Prychia paalonga (Barrion & Litsinger, 1995) comb. nov. One species is transferred from Olios to the family Clubionidae Wagner, 1887: Clubiona paenuliformis (Strand, 1916a) comb. nov.

One species of the louse genus Philopterus Nitzsch, 1818 is redescribed and illustrated: Philopterus acrocephalus Carriker, 1949 ex Acrocephalus luscinius (Quoy & Gaimard, 1830), A. melanopogon (Temminck, 1823), A. scirpaceus (Hermann, 1804), A. schoenobaenus (Linnaeus, 1758), Iduna aedon rufescens Stegmann, 1929, I. rama (Sykes, 1832), Locustella sp. and L. ochotensis (von Middendorff, 1853). Philopterus acrocephalus represents the first species of the Philopterus-complex recorded in the family Locustellidae Bonaparte, 1854. Philopterus gustafssoni sp. nov. is described ex Regulus regulus (Linnaeus, 1758), R. regulus regulus (Linnaeus, 1758), R. regulus azoricus Seebohm, 1883, R. regulus buturlini von Loudon, 1911, R. regulus sanctaemariae Vaurie, 1954, R. regulus tristis Pleske, 1892 and R. ignicapillus (Temminck, 1820). Descriptions of both species are amended with genetic data, DNA sequences of mitochondrial cytochrome oxidase I, nuclear hyp and TMEDE6; concatenated sequences are compared to the morphologically nearest species with genetic data available, Philopterus citrinellae (Schrank, 1776) and Philopterus fringillae (Scopoli, 1772). Holotype of Philopterus reguli (Denny, 1842) is pronounced to be a straggler, determination of other known material from Regulidae is changed for Philopterus gustafssoni sp. nov.