Статті в журналах з теми "1842-1909"

The female of Argia tupi Calvert, 1909 (BRAZIL, Mato Grosso, Chapada dos Guimarães National Park, Cachoeira do Marimbondo (15.4330° S, 55.7198° W, 370 m), 01 xi 2015) is described, illustrated and diagnosed based on comparison with sympatric species of Argia Rambur, 1842. We also augmented the description of Argia bicellulata (Calvert, 1909) female (BRAZIL, Mato Grosso, Chapada dos Guimarães National Park, Rio Paciencia (15.3438° S, 55.8322° W, 280 m), 25 x 2015).

The Afrotropical species of the genus Trichodes Herbst, 1792, are revised. Descriptions and a key to the eight valid species are provided. T. pretiosus Gorham, 1883, is placed in synonym with T. lepidus (Walker, 1871); T. unimaculatus Pic, 1938, is synonymized with T. penicillatus Schenkling, 1909. Lectotypes are designated for T. aulicus Klug, 1842, and T. lepidus (Walker, 1871).

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.

The Brazilian fauna of Lestidae contains two genera (Archilestes Selys, 1862 and Lestes Leach in Brewster, 1815) with 14 species, many of which are poorly defined and/or known only by primary literature. To improve the knowledge of the Brazilian species of the genus Lestes we examined 97 specimens pertaining to 11 of the 13 described species. Additionally, a new species is described here in honor to Prof. Dr. Paulo De Marco Júnior: Lestes demarcoi (Holotype and Allotype: Brazil: Amazonas, Manaus, Reserva Adolpho Ducke, Acará trail, 02º55’46” S & 59º58’22” W, 62 m, 13.iv.2009, collected in tandem, U.G. Neiss leg. and deposited in FAAL). Diagnostic illustrations of all species are provided. Color photographs of live individuals of Lestes dichrostigma Calvert, 1909, Lestes forficula Rambur, 1842 and Lestes paulistus Calvert, 1909 are also presented.

Three new species are described here: Oxyagrion zielmae sp. nov. (Coenagrionidae) from one male collected at Costa Rica, Mato Grosso do Sul state; Lestes fernandoi sp.nov. (Lestidae) from a pair from Imperatriz, Maranhão state and Perithemis capixaba sp. nov. (Libellulidae) from one male from Mutum Preto, Espírito Santo state, all deposited at Museu Nacional, Rio de Janeiro, Brazil. Oxyagrion zielmae is similar to O. pavidum Selys, 1876 but differs by having cerci and paraprocts the same size, pterostigma long and narrow and terminal segment of genital ligula with the two lobes larger than in O. pavidum. Lestes fernandoi is compared with L. auritus Hagen in Selys, 1862; L. bipupillatus Calvert, 1909; L. dichrostigma Calvert, 1909; Lestes falcifer Sjöstedt, 1918; L. forficula Rambur, 1842; L. minutus Selys, 1862 and L. paulistus Calvert, 1909. The new species is most similar to Lestes falcifer and L. paulistus, but differ by the peculiar color of pterothorax, caudal appendages and genital ligula. Perithemis capixaba is similar to P. mooma Kirby, 1889 but differs by having the first segment of vesica spermalis slowly rounded, in P. mooma this structure is trapezoidal. Illustrated keys to new species are included.

Resumo Este artigo é uma proposta de análise dos estudos geográficos, hidrográficos, botânicos e zoológicos elaborados pelo botânico brasileiro João Barbosa Rodrigues (1842-1909), em viagem pelo rio Capim entre os anos de 1874-1875. Esta viagem fez parte da Comissão Exploradora do vale do Amazonas, a qual foi liderada por Barbosa Rodrigues e contou com o patrocínio do Governo Imperial. Estes estudos se encontram no relatório “Exploração e estudo do Valle do Amazonas: rio Capim” publicado e apresentado em 1875 ao Ministério da Agricultura, Comércio e Obras Públicas.

Resumo Este artigo é uma proposta de análise dos estudos geográficos, hidrográficos, botânicos e zoológicos elaborados pelo botânico brasileiro João Barbosa Rodrigues (1842-1909), em viagem pelo rio Capim entre os anos de 1874-1875. Esta viagem fez parte da Comissão Exploradora do vale do Amazonas, a qual foi liderada por Barbosa Rodrigues e contou com o patrocínio do Governo Imperial. Estes estudos se encontram no relatório “Exploração e estudo do Valle do Amazonas: rio Capim” publicado e apresentado em 1875 ao Ministério da Agricultura, Comércio e Obras Públicas.

A new species, Isotoma koreana sp. nov. is described. It is most similar to Isotoma pinnata Börner, 1909, I. riparia (Nicolet, 1842) and I. grana Lee, Kim & Kim, 1993, in possessing a middorsal longitudinal band on body. It can be distinguished in having a thin central stripe on dorsal side of body, the structure of manubrial apical spines and body chaetotaxy. Isotoma grana is redescribed here from type material and compared with related species. An indentification key to the Sino-Japanese species of Isotoma Bourlet is provided.

The genera Ameropterus Esben-Petersen, 1922 and Fillus Navás, 1919 are recorded from Colombia for the first time. New distributional records for two Cordulecerus Rambur, 1842 species are also presented. Ameropterus dissimilis (McLachlan, 1871) and Ameropterus scutellaris (Gerstaecker, 1894) are redescribed and illustrated, and Ameropterus mexicanus (Van der Weele, 1909) is here proposed as a junior synonym of the latter. The taxonomic status of Nephelasca crocea Navás, 1914 is discussed. Keys to the Colombian species of Ameropterus and Cordulecerus and a list of the split-eyed Ascalaphinae species of the New World are also given.

This study focused on Mantispidae species (Neuroptera) from Tocantins state in Brazil. Herein we provide nine new records to this state, increasing the total number of mantidflies from Tocantins to 12. New records are as following: Anchieta fumosella (Westwood, 1867); Dicromantispa moulti (Navás, 1909); Entanoneura batesella (Westwood, 1867); Haematomantispa sp.; Leptomantispa chaos Hoffman, 2002; Plega hagenella (Westwood, 1867); Trichoscelia varia (Walker, 1853); Zeugomantispa compellens (Walker, 1860); Z. virescens (Rambur, 1842). We also provide the first list of Mantispidae species from Tocantins, including general notes for each one, and identification key for these species.

The southern South American species of the genus Philonthus Stephens, 1829 (Staphylininae: Staphylinini) are revised using characters of external morphology and male and female genitalia. Three species of Philonthus are transferred to the genus Belonuchus Nordmann, 1837 resulting in the following new combinations: B. aluticollis (Bernhauer, 1921), B. flavicoxis (Bernhauer, 1912) and B. weiserianus (Bernhauer, 1921). Twenty-five valid species are recognized for the region in the present study: Philonthus aeruginosus Nordmann 1837, P. argus Herman 2001, P. bicoloristylus ChaniPosse 2004, P. bonariensis Bernhauer 1909, P. convexicollis Lynch-Arribálzaga 1884, P. cribriventris Bernhauer 1912, P. discoideus (Gravenhorst, 1802), P. figulus Erichson 1840, P. flavolimbatus Erichson 1840, P. hepaticus Erichson 1840, P. jenseni Bernhauer 1912, P. longicornis Stephens 1832, P. lynchi Bernhauer & Schubert 1914, P. pallipes Blanchard 1842, P. pauxillus Solsky 1868, P. politus (Linnaeus, 1758), P. quadraticeps Boheman 1858, P. rectangulus Sharp 1874, P. rubromaculatus Blanchard 1842, P. ruficauda Bernhauer 1934, P. sericans (Gravenhorst, 1802), P. stenocephalus Scheerpeltz 1972, P. varians (Paykull, 1789). Two new species are described: P. floresi and P. bruchianus. Philonthus feralis Erichson 1840, previously recorded for this region, is also redescribed. Diagnoses, redescriptions or descriptions, illustrations, bionomic information and distribution maps for all species are presented. An identification key to the southern South American species of the genus is provided. Lectotypes are designated for Philonthus aeruginosus Nordmann 1837, P. aluticollis Bernhauer 1921, P. apicipennis Lynch-Arribálzaga 1884, P. convexicollis LynchArribálzaga 1884, P. figulus Erichson 1840, P. flavicoxis Bernhauer 1912, P. jenseni Bernhauer 1912, P. pallipes Blanchard 1842, P. rubromaculatus Blanchard 1842, P. stenocephalus Scheerpeltz 1972, P. tucumanensis Bernhauer 1934 and P. weiserianus Bernhauer, 1921.

AbstractThis paper is a sequel to Fischel and Kark's study on the private lands owned by Sultan Abdülhamid II (1842-1918, ruled 1876-1909) in Palestine and analyzes their fate after his forced abdication. In particular, we examine the court cases that arose around these lands, cases which were initiated by his heirs after 1920. For 28 years the heirs, led by his eldest son, Mohammad Selim and his daughter Amina Namika, approached half a dozen governments in the Middle East and Europe to regain the properties they claimed. The appeals represented a test of the British colonial legal system as well as issues of land settlement and the role of foreign courts in interpreting Turkish and Ottoman law. We furthermore examine the disposition of the sultan's lands from his abdication in 1909 to the last attempts by his heirs to recover them from the State of Israel in 1950, the general context of his lands in the Middle East as a whole, and the legal precedent set by the Mandatory Palestine court cases.

Here we update the status of Brazilian Mantispidae (Neuroptera) species originally placed in the Old World genus Mantispa Illiger, 1798. We revised 15 species: Buyda phthisica (Gerstaecker, 1885), Dicromantispa debilis (Gerstaecker, 1888) (= Mantispa (Mantispilla) lineaticollis Enderlein, 1910, n. syn.), Dicromantispa gracilis (Erichson, 1839), Dicromantispa hyalina n. sp., Dicromantispa leucophaea n. sp., Dicromantispa moulti (Navás, 1909) n. comb., Dicromantispa synapsis Hoffman, 2002, Haematomantispa amazonica n. sp.; Leptomantispa ariasi (Penny, 1982) n. comb., Leptomantispa axillaris (Navás, 1908) n. comb., Leptomantispa catarinae Machado & Rafael, 2007, Leptomantispa chaos Hoffman, 2002, Leptomantispa nymphe Hoffman, 2002, Zeugomantispa compelens (Walker, 1860) (=Mantispa parvula Penny, 1982, n. syn.), Zeugomantispa virescens (Rambur, 1842). We also provide an illustrated key to subfamilies, genera and species.

North Atlantic and Arctic representatives of the family Pyramidellidae had been intensively studied during the last decades. A valuable contribution was made by Warén (1989; 1991; 1993), who partially revised several genera from the Scandinavian waters. Norwegian representatives of the family were reviewed by Høisæter (2014). Distribution and diagnostic of many species had been specified by Schander (1995) and Nekhaev (2011; 2014; 2017). However, in the Eurasian Arctic Seas (except for the SW Barents Sea) only five species of Pyramidellidae had been recorded (Golikov et al. 2001; Kantor & Sysoev 2006; Nekhaev 2017): Liostomia eburnea (Stimpson, 1851), Chrysallida sublustris (Friele, 1886), Amaura candida (Møller, 1842), Amaura arctica (Dall et Bartsch, 1909) and Menestho truncatula Odhner, 1915.

Considering the geographical location of China, a very rich fauna of water mites should be expected. Previously, seventeen families have been reported from China (Jin, 1997; Smit, 2002; Guo & Jin, 2005): Eylaidae Leach, 1815, Limnocharidae Grube, 1859, Hydryphantidae Piersig, 1896, Hydrodromidae Viets, 1936, Hydrachnidae Leach, 1815, Sperchontidae Thor, 1900, Lebertiidae Thor, 1900, Oxidae Viets, 1926, Teutoniidae Koenike, 1910, Limnesiidae Thor, 1900, Hygrobatidae Koch, 1842, Unionicolidae Oudemans, 1909, Pionidae Thor, 1900, Mideopsidae Koenike, 1910, Arrenuridae Thor, 1900 and Pontarachnidae Koenike, 1910. The species described in this paper belongs to the subgenus Dartia Soar, 1917 in the genus Nilotonia Thor, 1905 of the family Anisitsiellidae Koenike, 1910, which increases the number of known water mite families in the Chinese fauna to eighteen.

Resumo Em 1871, o botânico João Barbosa Rodrigues (1842-1909) foi comissionado pelo Governo Imperial para explorar alguns rios do vale amazônico, a fim de completar a parte das palmeiras da grandiosa “Flora Brasiliensis”, de Karl Friedrich Philipp von Martius (1794-1868). Foi assim que Barbosa Rodrigues explorou o rio Capim. Os resultados dessa viagem estão no Relatório “Exploração e estudo do valle do Amazonas: rio Capim”, no qual o botânico registrou não apenas minuciosa descrição geográfica e hidrográfica deste rio, como também aspectos botânicos, zoológicos e de ocupação humana da localidade por meio de observações arqueológicas e etnográficas. O objetivo deste artigo é estabelecer como os estudos realizados por Barbosa Rodrigues no rio Capim contribuíram para a elaboração de um conhecimento científico da Amazônia paraense, construído dentro do contexto político-científico brasileiro do século XIX, dominado pelo Instituto Histórico e Geográfico Brasileiro.

Nineteen geographical records for species of Odonata in 2 provinces of Argentina are documented. We provided records for 9 newly recorded species for Córdoba: Lestes spatula Fraser, 1946, Andinagrion peterseni (Ris, 1908), Argentagrion ambiguum (Ris, 1904), Erythemis attala (Selys in Sagra, 1857), Erythemis plebeja (Burmeister, 1839), Erythrodiplax media Borror, 1942, Micrathyria longifasciata Calvert, 1909, Micrathyria hypodidyma Calvert, 1906, and Tramea cophysa Hagen, 1867. In San Luis, we provided records for 10 newly recorded species: Hetaerina rosea Selys, 1853, Acanthagrion lancea Selys, 1876, Ischnura fluviatilis Selys, 1876, Oxyagrion rubidium (Rambur, 1842), Castoraeschna decurvata Dunkle & Cook, 1984, Rhionaeschna pallipes (Fraser, 1947), Phyllocycla argentina (Hagen in Selys, 1878), Erythrodiplax corallina (Brauer, 1865), Perithemis mooma Kirby, 1889, and Planiplax erythropyga (Karsch, 1891). Among these records, we extend the geographic distribution of A. peterseni and R. pallipes, which are endemic to Argentina and recorded P. erythropyga for the first time in Chaco phytogeographic province.

Un ejemplar adulto macho de Speothos venaticus Lund, 1842 fue muerto accidentalmente en una vía de penetración rural, situada en la región Noroeste del Estado Bolívar, Venezuela, en el Municipio donde desde hace 16 años vive una paciente con lagochilascariasis. El animal conservado durante un mes por congelación y desprovisto de su piel y cabeza fue autopsiado, hallándose en la tráquea dos especímenes adultos hembras y grávidos de Lagochilascaris sp., los cuales presentaban algunas características morfológicas de sus partes blandas diferentes a Lagochilascaris minor Leiper, 1909; entretanto, distintivos estables como son la forma de los interlabios, la localización de la vulva y particularmente el tamaño y número de las depresiones de la cáscara de los huevos, inclinan a pensar que se trata de aquel parásito, a pesar de no haberse hallado vermes machos que permitiesen el estudio de las espículas y su ducto eyaculador. Fueron localizadas en cortes histológicos de laringe y tráquea profundamente situadas, secciones de formas degeneradas con características atribuíbles a Lagochilascaris sp.

Three new species of Sephina Amyot and Serville 1843, are described: S. crassa from Ecuador, S. effrena from Colombia and S. ornata from Panama. A key to the 27 known species and photographs of the dorsal habitus are included. Also included are photographs of the male genital capsule of S. vinula Stål 1862, and parameres of S. indierae Wolcott 1924 and S. vinula. New distributional records for S. dorsalis (White 1842), S. esquivelae Brailovsky & Sánchez 1983, S. faceta Brailovsky 2001, S. formosa (Dallas 1852), S. geniculata Distant 1881, S. limbata Stål 1862, S. nigripes Schmidt 1907, S. pagella Brailovsky & Sánchez 1983, S. pubera (Erichson 1848), S. pustulata (Fabricius 1803), S. rogersi Distant 1881, S. subulata Brailovsky & Sánchez 1983, and S. vinula are included. Sephina excellens Schmidt, 1907 is synonymized under S. pubera (Erichson 1848). The synonymy of Sephina grayi Van Duzee, 1909 under S. gundlachi (Guérin-Méneville 1857) is here corroborated.

The fish fauna of urban streams is still poorly known, it difficult to assess the effects of urbanization expansion on fish species composition, for this reason the aim of this study was to provide a checklist of species that compose the ichthyofauna of six urban streams, tributaries to the Vermelho River, upper Paraguay River Basin, Rondonópolis, Mato Grosso State, Brazil. The samples were performed with seine nets on a spatial gradient of 75 m, and with sieves for a period of 15 minutes in each site. A total of 56 species belonging to five orders, Characiformes, Siluriformes, Gymnotiformes, Cyprinodontiformes, and Perciformes, 21 families and 44 genera were sampled. The most common species were Astyanax asuncionensis Géry, 1972, Astyanax abramis (Jenyns, 1842), Odontostilbe pequira (Steindachner, 1882), Odontostilbe paraguayensis Eigenmann & Kennedy, 1903, Characidium zebra Eigenmann, 1909 and Hypostomus sp. This checklist brings additional knowledge on fish that inhabit tributaries to the major rivers of northern Pantanal.

Objective of research: to perform the analysis of long-term (15 annum) dynamics of Bithyniidae snails infected by trematode parthenites from the Chany Lake, the biggest lake in the south of Western Siberia. Materials and methods: The Bithyniidae snails examined in the lake-river systems Chany Lake in 1994-2013 (in the middle reaches and in the estuary of the Kargat River) and in the Zolotye Rossypi Bay and the Malye Chany Lake. The Bithyniidae snails were collected from May to September (twice in any ten days) by hand from 4–6 plots of 0.25 m2 at a depth of 0.1–0.7 m. In total, 8,316 Bithynia troscheli (Paasch, 1842) and 766 В. tentaculata (L., 1758) were examined. Identification of parthenitae trematode was based on observation when mature cercariae were capable of leaving the shell of the host snail on their own. Results and discussion: In Bithyniidae snails, we found parthenites from trematodes from 12 families Cyathocotylidae Mühling, 1898 Poche, 1925; Prosthоgonimidae Luhe, 1909; Pleurogenetidae Looss, 1898; Lecithodendriidae Odhner, 1911; Microphallidae (Ward, 1901) Travassos, 1920; Plagiorchiidae Lühe, 1901 Echinostomatidae (Looss 1899) Dietz, 1909 Odhner 1910); Psilostomidae (Looss 1900) Odhner 1913; Notocotylidae Luhe, 1909; Monorchiidae Odhner, 1911; Cyclocoelidae Kossack, 1911 и Opisthorchidae (Lass, 1899) Braun, 1901. The prevalence of bithyniid snails infected by trematode parthenites varied from 1,6% to 24,1% in different years The double infection by trematode parthenites was found in 0,96% bithyniid snails from estuary of the Kargat River; 4,45% in the Malye Chany Lake, and 26,6%, in the Zolotye Rossypi Bay. The cercariae of Opisthorchidae family in four annum of the fifteen detected. The prevalence of bithyniid snails infected by trematode parthenites from Opisthorchis felineus (Rivolta, 1884) and Metorchis bilis (Braun, 1890) was observed in Chany Lake systems for the first time. Both species (O. felineus and M. bilis) of trematodes have danger to human health and causes very dangerous disease, opisthorchiasis and metorchiasis.

La escritora peruana Mercedes Cabello de Carbonera (1842- 1909), como parte de su proyecto de novela moderna, publicó seis novelas en las que representó la sociedad limeña anterior a la Guerra del Pacífico (1879- 1883). La última de ellas se titula El Conspirador. Autobiografía de un hombre público. Novela político-social (1892) y es también la que mejor problematiza, a través de la parodia, el proyecto ético-estético de su autora. En este artículo, analizamos tres aspectos: el travestismo de los personajes, la carnavalización de la ciudad letrada y la reflexión metaliteraria a través del género autobiográfico. Creemos que a través de ellos se configura una estilización paródica (Bajtin, Hutcheon, Tran-Gervat) de distintos géneros vigentes en la segunda mitad del siglo XIX (novela política, novela picaresca, relato de costumbres, novela sentimental) que le permite a la autora, por un lado, reescribir y subvertir su propia intencionalidad realista reflejada en la denominación “político-social”, y por el otro, reflexionar acerca del valor de la novela como instrumento civilizatorio.

AbstractA survey of cercariae and metacercariae (Trematoda, Digenea) from bithyniid snails (Gastropoda: Bithyniidae) in lake-river systems in Northern Kulunda (of the steppe zone of the West Siberia Plain) is presented. The role of Bithynia tentaculata (Linne, 1758) and Bithynia troscheli (Paasch, 1842) as the first intermediate hosts and as the second intermediate hosts of trematodes in the study area was accomplished for the first time. Twelve species of cercariae (8 families) and 12 species of metacercariae (6 families) were found in bithyniid snails. Altogether, bithyniid snails were infected with 23 trematode species including 16 genera in 11 families. New Cercariae Holostephanus sp. and five original species of trematode metacercariae, were discovered in bithyniid snails of the steppe zone of the West Siberia Plain. The dominant cercariae were those of the families Prosthogonimidae and Lecithodendriidae. The most prevalent metacercariae were Echinoparyphium aconiatum Dietz, 1909 and E. recurvatum Linstow, 1873 (both family Echinostomatidae) and Cyathocotyle bithyniae Sudarikov, 1974 (Cyathocotylidae). B. troscheli infected by trematode parthenitae of Holostephanus sp. was detected in the Russia for the first time.

The Neotropical Mycotretus Lacordaire, 1842 is one of the largest and most widespread genera of the Erotylidae, encompassing more than 200 described species. Among the species with a similar body coloration, there is a “group” of six valid species—called here the “tiger” Mycotretus—that possess several pronotal and elytral black spots, as follows: M. tigrinus (Olivier, 1792); M. multimaculatus Taschenberg, 1870; M. centralis Arrow, 1909; M. tigrinoides Mader, 1942; M. tigripennis Mader, 1942; and M. prioteloides Mader, 1942. Different from any other Mycotretus with spots, the spots of the “tiger” Mycotretus are numerous and are not bilaterally symmetrical in pattern. Here, new geographical records, diagnoses and redescriptions are provided for M. tigrinus, M. centralis, M. tigrinoides, M. tigripennis and M. prioteloides, including the first descriptions of their male and female terminalia. Lectotypes are designated for M. multimaculatus, M. centralis, and M. leopardus. Mycotretus multimaculatus and M. tigrinus pardalis Crotch, 1876 are proposed as new junior synonyms of M. tigrinus. Additionally, the authorship of the name M. leopardus is attributed to Crotch, 1876, because he was the first author to provide a description for that taxon, and the synonymy of M. leopardus and M. conspersus (Germar, 1824) with M. tigrinus (Olivier, 1792) is confirmed.

Redescriptions are provided of Otobothrium carcharidis (Shipley & Hornell, 1906), O. crenacolle Linton, 1890, O. curtum (Linton, 1909) and O. propecysticum Dollfus, 1969 based on the type specimens and new material collected from elasmobranch hosts from Australia, Malaysia and New Caledonia. All are considered to be valid species. A neotype has been designated for O. crenacolle. A new species, O. parvum, is described from the spiral valve of Carcharhinus amblyrhynchos (Bleeker, 1856) and Triaenodon obesus (Rüppell, 1837) from New Caledonia. Otobothrium minutum Subhapradha, 1955 is considered to be a valid but poorly described species, being differentiated on the basis of a lack of testes posterior to the ovary. Otobothrium cysticum (Meyer, 1842) is considered a species inquirenda. The presence of an hermaphroditic sac is a new character for the genus while O. curtum lacks bothrial pits, a characteristic found in all congeners examined. The species described or redescribed here can be distinguished based on the number of segments and the number and distribution of testes, in addition to the features of the scolex. Otobothrium crenacolle is readily distinguished by its larger bothrial pits. The metabasal armature begins on either the bothrial or internal surface of the tentacle depending upon the species.

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.

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).

Around 1970 Tjeder suggested two changes to the nomenclature of the Ascalaphidae regarding the names Libelloides and libelluloides. To avoid future confusion, we augment Tjeder’s work by analyzing the nomenclatural status of all taxa related to these names—specifically Libelloides Schäffer, 1763 and Libelloides coccajus ([Denis et Schiffermüller], 1775), Ascalaphidae, and Palpares libelluloides (Linnaeus, 1764), Myrmeleontidae. After a short historical preamble, we treat the three taxa in chronological order of description. Additional information is reported in four Addenda, followed by a list of synonymies. Our conclusions are as follows: 1. Schäffer’s Das Zwiefalter– oder Afterjüngferchen (1763) is consistent with the Principle of Binomial Nomenclature, thus the names Libelloides and Libellula spuria, therein created, are available [ICZN Code Article 11.4.1.]. 2. Libellula spuria Schäffer, 1763, is a senior synonym of Papilio coccajus [Denis et Schiffermüller], 1775; however, the older name Libellula spuria Schäffer, 1763, is a nomen oblitum with respect to the younger name Papilio coccajus [Denis et Schiffermüller], 1775, which therefore must be considered a nomen protectum [ICNZ Code Article 23.9.2: both Articles 23.9.2.1 and 23.9.2.2 apply]. 3. The name Hemerobius libelloides Linnaeus, 1764, is the correct original spelling [ICNZ Code Article 32.5.1 does not apply], but the subsequent spelling Myrmeleon libelluloides Linnaeus, 1767, even if an unjustified emendation [ICZN Code Article 33.2.1 and 33.2.3], is in prevailing usage and consequently: i) it is deemed to be a justified emendation, and ii) it is attributed to its original author and date [ICZN Code Article 33.2.3.1]. 4. Myrmeleon libelluloides Fuesslin, 1775, being a mere misidentification of the name Myrmeleon libelluloides (Linnaeus, 1764), is unavailable name [ICZN Code Article 49]. 5. Schäffer (1763) is not the author of the name Ascalaphus libelluloides: the authorship must be attributed to van der Weele with the date of description 5th January 1909. 6. Libellula turcica Petiver & Empson, 1767, in Ábrahám (2012), is an unavailable name. 7. The original spelling Myrmeleon kolywanense Laxmann, 1770, is the correct original spelling [ICNZ Code Article 32.5.1 does not apply], but the subsequent spelling Ascalaphus kolyvanensis Rambur, 1842, even if an unjustified emendation [ICZN Code Article 33.2.1 and 33.2.3], is in prevailing usage and consequently: i) it is deemed to be a justified emendation, and ii) it is attributed to its original author and date [ICZN Code Article 33.2.3.1]. 8. Fuesslin’s Verzeichniss der ihm bekannten schweizerischen Insekten (1775) was published between 24th February (date in the second part of the Preface [Vorrede]) and 12th May 1775 (Wyttenbach, 1775), so the date of publication is 12th May 1775 [ICZN Code Article 21.3].

The Australopacific Saprininae, containing twelve genera and forty species, are reviewed, illustrated and keyed to genera and species. Two new genera, Australopachylopusgen. n. (New Zealand, type species Saprinus lepidulus Broun, 1881) and Iridoprinusgen. n. (Australia, type species I. myrmecophilussp. n.) and four new species: Saprinus (Saprinus) rarussp. n. (Australia), Saprinus (Saprinus) chathamensissp. n. (Chatham Islands, New Zealand), Saprinus (Saprinus) pseudodetritussp. n. (Chatham Islands, New Zealand) and Saprinus (Saprinus) pacificussp. n. (Kiribati) are described. The Saprininae fauna of the Australopacific Region is a mixture of northern invaders that most likely arrived to the region in early Cenozoic by ‘island hopping’ from north (Hypocaccus, Hypocacculus, several Saprinus) and truly autochthonous taxa either with uncertain phylogenetic affinities (Iridoprinusgen. n., Saprinodes Lewis, 1891, Reichardtia Wenzel, 1944, Australopachylopusgen. n.), primitive Australopacific endemics (e.g. Tomogenius Marseul, 1862) or presumed relicts (several species of Saprinus Erichson, 1834). Several Saprininae taxa (Chalcionellus aeneovirens (Schmidt, 1890); (Gnathoncus rotundatus (Kugelann, 1792); G. communis (Marseul, 1862); Euspilotus (Neosaprinus) rubriculus (Marseul, 1855); Hypocaccus (Nessus) interpunctatus interpunctatus (Schmidt, 1885); Saprinus (S.) chalcites (Illiger, 1807) and Saprinus (S.) cupreus Erichson, 1834)) were introduced into the region with human activity. We report the first cases of myrmecophily (Iridoprinus myrmecophilusgen. et sp. n.) and termitophily (Saprinus rarussp. n.) in the Saprininae from the Australopacific Region. Lectotypes and paralectotypes of the following taxa are designated herein: Saprinus amethystinus Lewis, 1900, Saprinus apricarius Erichson, 1834, Saprinus artensis Marseul, 1862, Saprinus auricollis Marseul, 1855, Saprinus australasiae Blackburn, 1903, Saprinus bistrigifrons Marseul, 1855, Saprinus certus Lewis, 1888, Saprinus communis Marseul, 1862, Saprinus cupreus Erichson, 1834, Saprinus cyanellus Marseul, 1855, Hister cyaneus Fabricius, 1775, Saprinus dentipes Marseul, 1855, Saprinus desbordesi Auzat, 1916, Saprinus gayndahensis MacLeay, 1871, Saprinus hyla Marseul, 1864, Saprinus incisisternus Marseul, 1862, Saprinus incisus Erichson, 1842, Saprinus irinus Marseul, 1862, Saprinus laetus Erichson, 1834, Saprinus lepidulus Broun, 1881, Saprinus mastersii MacLeay, 1871, Saprinus nitiduloides Fairmaire, 1883, Saprinus pedator Sharp, 1876, Saprinus pseudocyaneus White, 1846, Saprinus rubriculus Marseul, 1855, Saprinus sinae Marseul, 1862, Saprinus tasmanicus Marseul, 1855, Saprinus tyrrhenus Blackburn, 1903, Saprinus varians Schmidt, 1890, Saprinus vernulus Blackburn, 1903, Saprinus viridanus Lewis, 1899, Saprinus viridipennis Lewis, 1901, and Saprinus westraliensis Blackburn, 1903. The synonymy of Saprinus tyrrhenus Blackburn, 1903 is revoked and the species is considered as valid (stat. n.). Seven new synonymies are proposed: Saprinus gayndahensis MacLeay, 1871 = Saprinus laetus Erichson, 1834 syn. n., Saprinus pseudocyaneus White, 1846 = Saprinus laetus Erichson, 1834 syn. n., Saprinus mastersii MacLeay, 1871 = Saprinus laetus Erichson, 1834 syn. n., Saprinus dentipes Marseul, 1855 = Hypocaccus (Baeckmanniolus) gaudens (J.L. LeConte, 1851) syn. n., Hypocaccus (Hypocaccus) vernulus (Blackburn, 1903) = Hypocaccus (Hypocaccus) sinae (Marseul, 1862) syn. n., Saprinus (Saprinus) lindrothi Dahlgren, 1968 = Saprinus (Saprinus) prasinus Erichson, 1834 syn. n., and Saprinus (Saprinus) certus Lewis, 1888 = Saprinus (Saprinus) frontistrius Marseul, 1855 syn. n. The following new records are: Euspilotus (Neosaprinus) rubriculus (Marseul, 1855) (= Saprinus gnathoncoides Bickhardt, 1909) (Australia), Saprinus (Saprinus) laetus Erichson, 1834 (Lord Howe Island) and Saprinus (Saprinus) cyaneus cyaneus (Fabricius, 1775) (Lord Howe Island and Fiji).

The limits of Lyrcus Walker (1842), Catolaccus Thomson (1878), Eurydinoteloides Girault (1913a), Trimeromicrus Gahan (1914), and Jaliscoa Bouček (1993) are re-evaluated and redefined to better reflect observed distribution of morphological features. Nine of 13 New World species of Catolaccus are transferred to other genera and photographs of the primary type specimens are given to assist future recognition. New features are provided to assist identification of the remaining four Nearctic species of Catolaccus and these are compared to European species, with the observation that C. kansensis (Girault 1917c) could be a junior synonym of C. crassiceps (Masi 1911). Trimeromicrus is removed from synonymy under Lyrcus for the single species T. maculatus Gahan (1914) rev. comb. Newly synonymized under Lyrcus is the Australasian genus Neocylus Bouček (1988) n. syn. Ten species are newly transferred to Lyrcus—L. nigraeneus (Girault 1915) n. comb. (from Neocylus), L. helice (Walker 1843) n. comb. and L. cyaneus (Girault 1911) n. comb. (from Catolaccus), and L. albiclavus (Girault 1917c) n. comb., L. capitis (Burks 1955) n. comb., L. chalcis (Burks 1955) n. comb., L. coeliodis (Ashmead 1896) n. comb., L. deuterus (Crawford 1911) n. comb., L. nigroaeneus (Ashmead 1894a) n. comb. and L. rosaecolis (Burks 1955) n. comb. (from Zatropis Crawford 1908). Catolaccus pallipes Ashmead (1894b) is newly transferred to Pteromalus Swederus (1795) as Pteromalus pallipes (Ashmead) n. comb. and Catolaccus fragariae Rohwer (1934) to Lariophagus Crawford (1909) as Lariophagus fragariae (Rohwer) n. comb. Nine species are newly transferred to Eurydinoteloides—E. tepicensis (Ashmead 1895) n. comb. (from Catolaccus), E. dymnus (Walker 1847) n. comb., E. hermeas (Walker 1847) n. comb., E. incerta (Ashmead 1893) n. comb., E. orontas (Walker 1847) n. comb., E. perdubia (Girault 1916) n. comb., E. platensis (De Santis in De Santis et al. 1979) n. comb. and E. timaea (Walker 1847) n. comb. (from Lyrcus), and E. eudubia (Özdikmen 2011) n. comb. (from Spintherus Thomson 1878). Four species are newly transferred to Jaliscoa—J. grandis (Burks 1954) n. comb. and J. hunteri (Crawford 1908) n. comb. (from Catolaccus), and J. townsendi (Crawford 1912) n. comb. and J. vulgaris (Ashmead 1894b) n. comb. (from Pteromalus). The species of Jaliscoa are revised to include J. nudipennis Bouček 1993, J. bouceki n. sp., J. hunteri and J. vulgaris. Re-established in synonymy under J. hunteri is J. townsendi n. comb. One new species of Pteromalus, P. grisselli n. sp., is described as an egg predator in the egg sacs of Dictyna coloradensi Chamberlin (Araneae: Dictynidae) and compared to Catolaccus species and other pteromalids that are predators of spider eggs. Lectotypes are designated for Pteromalus helice Walker (1843), Catolaccus pallipes Ashmead (1894b) and Catolaccus vulgaris Ashmead (1894b). Diagnoses are given to differentiate Catolaccus, Eurydinoteloides, Jaliscoa, Lyrcus and Trimeromicrus from each other, and more extensive descriptions given to help differentiate these genera from other Pteromalinae. Morphological features are illustrated through macrophotography and scanning electron photomicrography.

The taxonomy of the New Zealand weevil genus Irenimus Pascoe, 1876 is revised, resulting in a narrower concept of the genus than has been considered in recent decades. In total, the genus now contains only seven species. In addition to the type species, I. parilis Pascoe, 1876, the genus contains I. duplex (Broun, 1904) and five newly described species: I. aniptus new species (type locality, Oamaru, DN), I. crinitus new species (type locality, Hakataramea Valley, SC), I. minimus new species (type locality, Alexandra, CO), I. stichus new species (type locality, Tekapo, MK) and I. thoracicus new species (type locality, Oamaru, DN). The genus Chalepistes new genus is established to contain the majority of species previously described in the genus Catoptes Schönherr, 1842, but also including species described in Brachyolus White, 1846; Irenimus Pascoe, 1876; Inophloeus Pascoe, 1875; and Nicaeana Pascoe, 1877. A total of 27 valid described species are new combinations with Chalepistes: C. aequalis (Broun, 1895) (from Irenimus), C. albosparsus (Broun, 1917) (from Irenimus), C. apicalis (Broun, 1923) (from Catoptes), C. asperatus (Broun, 1914) (from Brachyolus), C. compressus (Broun, 1880) (from Irenimus), C. costifer (Broun, 1886) (from Inophloeus), C. curvus (Barratt & Kuschel, 1996) (from Irenimus), C. dehiscens (Broun, 1917) (from Catoptes), C. dugdalei (Barratt & Kuschel, 1996) (from Irenimus), C. egens (Broun, 1904) (from Irenimus), C. inaequalis (Sharp, 1886) (from Brachyolus), C. instabilis (Marshall, 1931) (from Catoptes), C. latipennis (Broun, 1893) (from Catoptes), C. limbatus (Broun, 1909) (from Catoptes), C. lobatus (Broun, 1921) (from Catoptes), C. patricki (Barratt & Kuschel, 1996) (from Irenimus), C. pensus (Broun, 1914) (from Inophloeus), C. placidus (Broun, 1914) (from Nicaeana), C. posticalis (Broun, 1893) (from Irenimus), C. rhesus (Pascoe, 1875) (from Inophloeus), C. rubidus (Broun, 1881) (from Inophloeus), C. similis (Barratt & Kuschel, 1996) (from Irenimus), C. spectabilis (Broun, 1914) (from Catoptes), C. spermophilus (Broun, 1895), revised status (from Irenimus), C. stolidus (Broun, 1886) (from Irenimus), C. tenebricus (Broun, 1893) (from Catoptes), C. vastator (Broun, 1893) (from Irenimus). Numerous new synonyms with species of Chalepistes are also proposed: Brachyolus fuscipictus Broun, 1914 and Brachyolus terricola Broun, 1917 are junior subjective synonyms of Chalepistes asperatus (Broun); Brachyolus cervalis Broun, 1903 and Brachyolus sylvaticus Broun, 1910 are junior subjective synonyms of Chalepistes costifer (Broun); Inophloeus tricostatus Broun, 1915 is a junior subjective synonym of Chalepistes pensus (Broun); Catoptes pallidipes Broun, 1917, Catoptes flaviventris Broun, 1917 and Catoptes nigricans Broun, 1917 are junior subjective synonyms of Chalepistes placidus (Broun); Inophloeus longicornis Broun, 1904, Inophloeus medius Broun, 1893, Inophloeus sulcicollis Broun, 1914 and Inophloeus suturalis Broun, 1893 are junior subjective synonyms of Chalepistes rhesus (Pascoe); Inophloeus albonotata Broun, 1893, Catoptes asperellus Broun, 1893, Irenimus bicostatus Broun, 1886, Catoptes caliginosus Broun, 1893, Catoptes chalmeri Broun, 1893, Catoptes decorus Broun, 1893, Inophloeus discrepans Broun, 1904, Catoptes fumosus Broun, 1914, Catoptes furvus Broun, 1893, Catoptes humeralis Broun, 1893, Catoptes longulus Sharp, 1886, Inophloeus nigellus Broun, 1881, Irenimus pilosellus Broun, 1886 and Catoptes scutellaris Sharp, 1886 are junior subjective synonyms of Chalepistes rubidus (Broun); Catoptes subnitidus Broun, 1914 and Catoptes curvatus Broun, 1914 are junior subjective synonyms of Chalepistes spermophilus (Broun); Catoptes brevicornis Sharp, 1886 and Catoptes vexator Broun, 1904 are junior subjective synonyms of Chalepistes stolidus (Broun); and Catoptes aemulator Broun, 1893 and Catoptes argentalis Broun, 1914 are junior subjective synonyms of Chalepistes tenebricus (Broun). Additional new combinations include Inophloeus robustus (Broun, 1917) (from Catoptes) and Nicaeana fraudator (Marshall, 1931) (from Catoptes), while Catoptes postrectus Marshall, 1931 is a new synonym of Protolobus obscurus Sharp, 1886.

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.

Abstract The article analyzes the narratives of three travels along the Capim River, in the state of Pará, Brazil, between 1849 and 1897: those of Alfred Russel Wallace (1823–1913), João Barbosa Rodrigues (1842–1909) and Emil Goeldi (1859 –1917), who traveled with another scientist, Jacques Huber (1867–1914). These are considered the first scientists to explore the river and publish work on it. We highlight the intertextuality of their reports and also the process of knowledge translation between travelers and their interlocutors, an approach that we consider necessary and unavoidable for the development of this field of investigation. Our main sources are published narratives, sometimes associated with manuscripts and iconography.

Abstract The article mentions aspects of the collections gathered in the Amazon Botanical Museum (Museu Botânico do Amazonas), directed by João Barbosa Rodrigues (1842-1909). It presents evidence of the continued circulation of some objects from these collections, even after the formal extinction of the Museum, which existed for seven years from 1883 to 1890. The interest of this article is to encourage further research on the subject of the circulation of collections and their proxies, to recover stories of donors, objects and museums that have been lost, in different times and places in the country, in order to value our continuously neglected scientific heritage.

Caricature, in a historical sense, can be deemed as an application that reveals a human’s ability to paint. It is perceived that the caricature, which has been held in human life since cave paintings until today, has also a unique place in our modern life with different ways and various fields through the course of history. The caricature will continue to exist as an influential representative in the combination of painting and criticism. In this context, political caricatures are one of the most practical and efficient methods used to criticize notables of states. The dose of these caricatures is caused many controversies even today, as they increase their violence and cruelty in case of conflicts between states. There are many media outcomes published in Europe that collect with the developments worldwide. It is reasonable to confer following newspapers and magazines as examples in this field: La Silhouette (1829), La Caricature (1830), Penny Magazine (1832), Punch (1841), L’Illustration Journal Universel (1843), Harpers’s Magazine (1850), Le Monde Illustré (1857), The Illustrated London News (1842), Frank Leslie’s Illustrated News (1855), Puck (1871) etc. These newspapers and magazines have a unique place in the world press history in terms of showing all varieties of criticism, apart from being pioneers in many fields. Since these publications systematically followed the political and social events happening all over the world and included many illustrations, caricatures and columns on various topics according to the agenda. These descriptions are noteworthy documents for many disciplines today. In recent years, access to works has increased with the convenience provided by digitalization. Therefore, the descriptions in various printed publications have emerged in a way that supports the studies in many types of research, even with the potential to be the main topic directly. The journal, which addresses many people and issues critically, mainly in France and Europe, has established many studies on the Ottoman Empire and its leaders. Abdülhamid II (1876-1909), has been the subject of a notable amount of critical caricature during his long reign. Within the scope of this research, 15 caricatures that themed Abdülhamid II, which were selected from 836 numbers of Le Rire, published between 1894 and 1909, were determined and examined. The following subjects are processed in these caricatures: Some difficulties experienced by the Ottoman Empire in the Balkans and Eastern Anatolia, the rapprochement with the Germans, the endless negotiations in foreign policy, the turmoil in terms of the Ottoman sultanate and the joint studies with Europe. It is aimed to bring these caricatures, some of which are anonymous and some signed, as a consequence of various technical skills, to several fields of study and especially to the literature of art history by analyzing them in artistic and historical terms. Thus, Sultan Abdülhamid II, who had a very important share in the last years of the Ottoman Empire, has been the goal to reveal how Abdülhamid II was introduced or presented to the reader through the caricature.