342,433 research outputs found
DAISIErobustness: Test the Robustness of DAISIE to Geodynamics and Traits
No full textConducts a robustness test of the island biogeography DAISIE model to the effects of geodynamics or trait dependency. Tests processes such as island ontogeny, sea-level change and land-bridge dynamics. Contains acessory code for easy use with the University of Groningen Peregrine HPCC.See v1.0.1 patch notes at: https://github.com/Neves-P/DAISIErobustness/releases/tag/v1.0.
Setacheres Borges & Neves & Johnsson 2017
No full textKey to the species of <i>Setacheres</i> <p>1 Basis of leg 1 armed with 1,0........................................................................... 2</p> <p>- Basis of leg 1 armed with 1,I............................................................................ 3</p> <p> 2 Second endopodal segment of leg 4 armed with 0,1..................................... <i>S. ventricosus</i> (Brian, 1928)</p> <p> - Second endopodal segment of leg 4 armed with 0,2..................................... <i>S. lunatus</i> (Johnsson, 1998)</p> <p> 3 Female antennule 18-segmented..................................................... <i>S. unicus</i> (Johnsson, 2001)</p> <p>- Female antennule at least 19-segmented.................................................................. 4</p> <p>4 Female antennule 19-segmented......................................................................... 5</p> <p>- Female antennule at least 20-segmented.................................................................. 8</p> <p> 5 Mandibular palp 1-segmented.................................................... <i>S. aplysinus</i> (Johnsson, 2002)</p> <p>- Mandibular palp 2-segmented........................................................................... 6</p> <p> 6 Maxilliped endopod 4-segmented................................................ <i>S. spinopaulus</i> (Johnsson, 1998)</p> <p>- Maxilliped endopod at least 5-segmented.................................................................. 7</p> <p> 7 Maxillule with 3 setae on each lobe........................................... <i>S. picinguabensis</i> (Johnsson, 2001)</p> <p> - Maxillule with 4 setae on each lobe.............................................. <i>S. abrolhensis</i> (Johnsson, 1998)</p> <p> 8 Free segment of leg 5 armed with 2 setae......................................... <i>S. paraboecki</i> (Johnsson, 1998)</p> <p>- Free segment of leg 5 armed with 3 setae.................................................................. 9</p> <p> 9 Maxilliped endopod 5-segmented.................................... <i>S. eudistomus</i> Johnsson, Bahia & Neves, 2016</p> <p> - Maxilliped endopod 6-segmented..................................................... <i>S. portobarrensis</i> <b>sp. nov.</b></p>Published as part of <i>Borges, Camila C., Neves, Elizabeth G. & Johnsson, Rodrigo, 2017, A new Setacheres (Copepoda, Siphonostomatoida, Asterocheridae) associated with Ircinia felix (Duchassaing & Michelotti) (Porifera) from Brazil, pp. 129-136 in Zootaxa 4363 (1)</i> on page 135, DOI: 10.11646/zootaxa.4363.1.6, <a href="http://zenodo.org/record/1096315">http://zenodo.org/record/1096315</a>
Corpo, de Leandro Neves Cardim
No full textResenha do livro de: CARDIM, Leandro Neves Corpo. Col. Filosofia Frente & Verso. Sáo Paulo: Globo, 2009. 177 p
The theatrical work of João das Neves in the Grupo Opinião
No full textTendo-se realizado uma pesquisa de mestrado em que se objetivou examinar os aspectos constitutivos do pensamento crítico de João das Neves a partir do processo de investigação e análise de seus trabalhos em teatro no pré-64, projetou-se dar sequência história a esse estudo na tese agora apresentada, centrando-se em sua atuação no contexto político da ditadura militar brasileira. Desse modo, pretendeu-se verificar quais aspectos de seu pensamento mantêm-se e quais prevalecem em suas propostas no Grupo Opinião. Para tanto, foram analisadas várias frentes de engajamento de Neves, a fim de se compreender o papel desempenhado pelo artista para a criação e manutenção do grupo entre os anos 1964 e 1980. Nesse sentido, destacam-se aqui os seguintes temas investigados: o primeiro espetáculo do grupo, o Show Opinião; o Concurso e o Seminário de Dramaturgia Opinião, idealizados e organizados por João das Neves da década de 1970; a escrita e a encenação de O último carro, talvez a peça mais conhecida do autor; sua apropriação da ideia brechtiana de modelo; a pesquisa de Neves sobre a peça radiofônica alemã e o intercambio artístico iniciado e difundido por ele entre o Brasil e Alemanha; as particularidades cênico-dramatúrgicas de Mural mulher, última peça que se apresenta no espaço do Opinião; sua definição pelo teatro documentário e popular. Além das peças teatrais de João das Neves e da fortuna crítica, as análises foram construídas com base em documentos primários levantados, em declarações e depoimentos do autor em diferentes momentos e em entrevista realizada diretamente com ele. Por fim, vale dizer que, ao evidenciar as transformações decorrentes do período ditatorial, o exame do trabalho teatral de João das Neves no Grupo Opinião enseja uma aproximação do processo cultural brasileiro das últimas cinco décadas, contribuindo, portanto, para uma melhor compreensão do cenário artístico atual.Having conducted a master\'s degree research in which the objective was to examine the constitutive aspects of João das Neves\' critical thought based on the investigation and analysis of his theatrical works in the years prior to 1964, the project was to give historical continuity to this study in doctoral dissertation now presented, focusing on his work in the political context of the Brazilian military regime. In this way, the intention was to verify which aspects of his thought remain and which prevail in his proposals in Grupo Opinião. To this end, different aspects of Neves\' political engagement were analyzed in order to understand the role played by the artist in the creation and maintenance of the group between 1964 and 1980. In this sense, the following investigated themes to be noted are: the group\'s first play, Show Opinião; the Concourse and Seminar of Dramaturgy Opinião, conceived and organized by João das Neves in the 1970s; the writing and staging of O Último Carro, possibly the author\'s most known play; his appropriation of the Brecht\'s idea of model; Neves\' research on the German radio play and the artistic interchange initiated and spread by him between Brazil and Germany; the scenic-dramaturgical particularities of Mural Mulher, the last play performed at Opinião; his definition of documentary and popular theater. In addition to João das Neves\' plays and critical fortune, the analyses were built on primary documents surveyed, on statements and testimonials from the author at different times, and on interviews conducted with him. In addition to João das Neves\' plays and critical fortune, the analyses were built on primary documents surveyed, on statements and testimonials from the author at different times, and on interviews conducted with him. To conclude, it is Worth mentioning that showing the transformations of the dictatorship period, the examination of all theatrical work of João das Neves in Grupo Opinião presents a communion of the brazilian cultural process within the last five decades, providing a vast contribuition, nontheless, to a viable compreehension of the artistic scenario we see nowadays
Humidicutis pindorama J. S. Cardoso, M. A. Neves & J. S. Oliveira 2023, sp. nov.
No full text<i>Humidicutis pindorama</i> J.S. Cardoso, M.A. Neves & J.S. Oliveira, <i>sp. nov.</i> (Figs. 3a–e, 4a–c) <p>MycoBank # MB844321</p> <p> Etymology:—Refers to <i>Pindorama</i>, considered the indigenous name for Brazil in Tupi-Guarani language.</p> <p> Type:— BRAZIL. Santa Catarina: Itapoá, RPPN Volta Velha, Glass House Trail, 15 m elev., 26°05’23.4”S 48°38’18.5”W, 18 November 2012, <i>Cardoso, J. S. & Neves, M. A.</i> 18 (FLOR57148, holotype).</p> <p> Diagnosis:—Basidiomata green to orange, pileus umbonate, lamellae with orange edges, stipe with orangish small fibrils, context turning bluish when cut, growing solitary in white sandy soils. Differs from <i>Humidicutis multicolor</i> in the lack of purple-lilac-blue pigments in the basidiomata and by having bigger basidiospores.</p> <p> Description:— <i>Pileus</i> 22–35 mm diam., umbonate to papillate or plane with an umbo, sometimes split at the centre, smooth to finely fibrillose, moist to dry, moss green (oac41) to olive green (oac866, oac867) at the centre, becoming orange (oac838, oac775, oac789) towards the margin, hygrophanous, turning light brown (oac777) to brown (oac749) with age; margin even or slightly uplifted and splitting, sometimes eroded, translucent-striate, orange (oac761), orangy brown (oac842) with green tints, or light brown (oac799). <i>Lamellae</i> uncinate, subdistant, up to 3 mm broad, slightly intervenose, thick, very waxy, olive green (oac867, oac859) to moss green (oac41) near the insertion to pileus, then yellowish green (oac887) and yellowish orange (oac852, oac853) near the edge; edge entire, sometimes forking near the insertion to stipe, orange (oac761, oac789); lamellulae of two lengths. <i>Stipe</i> 20–50 mm × 3–4 mm, central, regular to irregular, hollow, sometimes with longitudinal fissure, dry, smooth to slightly fibrillose, green (oac40) to light green (oac67, oac851, oac21) at the apex, to yellowish (oac855) or orange (oac790, oac791) at the base, with orangish (oac845, oac810) superficial fibrils. <i>Pileus context</i> becoming slightly blue after cutting. <i>Basidiomata</i> becoming pinkorange when dried.</p> <p> <i>Basidiospores</i> 6.6– <i>7.98</i> –11 × 4– <i>5.61</i> –7 μm, Q = 1.422– <i>1.450</i> –1.470, ellipsoid, guttulate, thin-walled, hyaline, inamyloid, some germinating when still attached to the sterigmata. <i>Basidia</i> (29–)34–52.1 × 5.9–11 μm, cylindricclavate, funnel-shaped at the base, guttulate, hyaline, 4-spored, sterigmata up to 13.0 μm long, with conspicuous basal toruloid clamp-connections. <i>Lamellar edge</i> fertile. <i>Cystidia</i> absent. <i>Lamellar trama</i> regular to subregular, with parallel, slightly divergent hyphae, with some inflated segments, 33–197 × 3–40 μm, clamp connections absent. <i>Pileipellis</i> a cutis composed of slightly interlaced parallel hyphae, 3–9.4 μm diam., with granular encrusting pigments, some hyphae protruding, many branching or forming anastomosis, hyaline in KOH, light yellow in water, clamp connections absent. <i>Stipitipellis</i> a cutis of parallel hyphae 3.1–18 µm diam., cylindrical, septate, with granular encrusting pigments, with many anastomoses, upper layer of thin hair-like interwoven hyphae, 1–3.2 µm diam., protruding, hyaline in KOH, clamp connections absent.</p> <p> Specimens examined:— BRAZIL. Santa Catarina: Itapoá, RPPN Volta Velha, Glass House Trail, 15 m elev., 26°05’23.4”S 48°38’18.5”W, 18 November 2012, <i>Cardoso, J. S</i> <i>. & Neves, M. A.</i> 18 (FLOR57148); <i>Cardoso, J. S</i> <i>. & Neves, M. A.</i> 20 (FLOR 57150); Amazonas: Manaus, Cuieiras River INPA Reserve, 20 m elev., 2°34’06.7”S 60°19’15.2”W, 12 July 2018, <i>Cardoso, J. S</i> <i>. & Vieira, S. S.</i> 485 (INPA285626).</p> <p>Distribution:—Atlantic rainforest in Santa Catarina State and Amazon forest in Amazonas State.</p> <p> Habitat:—Growing solitary, on soil of white sand forests in both <i>restinga</i> and <i>campinarana</i> vegetation types.</p> <p> Comments:—There are seven green <i>Humidicutis</i> species described worldwide with only one recorded from South America, <i>Humidicutis multicolor</i> (Berk. & Broome) E. Horak (1990: 298). <i>Humidicutis multicolor</i> was described from Sri Lanka with records in Tierra del Fuego, Southern Argentina, and New Zealand (Horak 1979, Horak 1990). <i>Humidicutis multicolor</i> also has a blue pileus context when exposed but differs from <i>H. pindorama</i> by having purple-lilac-blue pigments in the pileus and stipe, and by the much smaller basidiospores (5.5–7 × 4–5 µm) and basidia (20–45 × 6–7 µm) (Horak 1990). <i>Humidicutis pindorama</i> is macroscopically like <i>Humidicutis luteovirens</i> (Horak) Horak (1990: 296) from New Zealand, but the latter has smaller basidiospores (6–8 × 3.5–4.5 µm) and basidia (25–42 × 6–7 µm) (Horak 1990). <i>Humidicutis arcohastata</i> (A.M. Young) A.M. Young (2005: 159) in Australia differs from <i>H. pindorama</i> by the conical to campanulate pileus and by the presence of purple-mauve tints on the pileus and stipe (Young 2005). <i>Humidicutis helicoides</i> (A.M. Young) A.M. Young (2005: 159) has lime green lamellae rather than green to orangy yellow lamellae with a deep orange edge (Young 2005). Also, <i>H. pindorama</i> lacks the spiral bands of encrusted pigments found in the pileipellis hyphae of <i>H. helicoides</i>. <i>Humidicutis taekeri</i> (A.M. Young) A.M. Young (2005: 159) is easily distinguished from <i>H. pindorama</i> by its brilliant orange lamellae (Young 2005). <i>Humidicutis viridimagentea</i> A.M. Young & K. Syme (2007: 71) differs by the distinctive magenta colouration (Young 2005, Young & Syme 2007). Finally, <i>Humidicutis woodii</i> (A.M. Young) A.M. Young (2005: 159) has a white stipe and lacks the conspicuous toroidal clamp connections (Young 2005) at the basidia base.</p> <p> Only the second species of <i>Humidicutis</i> known from South America, <i>H. pindorama</i> was described based on two specimens from Southern Brazilian Atlantic Rainforest and one from the Amazon Forest, increasing the distribution range of the genus. Basidiomata were found on white sand soils, so this species is probably adapted to soils poor in nutrients. The germinating basidiospores in JS20 are very intriguing and firstly recorded herein.</p>Published as part of <i>Cardoso, Juli Simon, Moncalvo, Jean-Marc, Lodge, D. Jean, Margaritescu, Simona, Neves, Maria Alice & Oliveira, Jadson J. S., 2023, Studies in Hygrocybe s. l. (Hygrocyboideae, Hygrophoraceae) in Brazil: New species of Humidicutis and Neohygrocybe, pp. 57-71 in Phytotaxa 607 (1)</i> on pages 63-64, DOI: 10.11646/phytotaxa.607.1.5, <a href="http://zenodo.org/record/8212211">http://zenodo.org/record/8212211</a>
Eustáquio Neves: photographic subject - memory and image
No full textEsta pesquisa tem como ponto de partida o acesso ao ateliê e aos arquivos de criação do artista Eustáquio Neves. A investigação dos percursos identificados nas obras, esboços, anotações e falas de Neves busca relações entre os processos de criação e a presença comunicante materializada nos trabalhados do artista, visando descobrir de que maneira os procedimentos adotados pelo autor transformam imagens em estandartes que carregam memórias deliberadamente evocadas enquanto povoam universo ficcional com seus próprios tempos e espaços. Neves coloca a fotografia no contexto das artes visuais ao criar imagens complexas nas quais o clamor político e as marcas do processo – tanto fotográfico quanto extrafotográfico – se impõem. A presença resulta, portanto, de investimento semântico que perpassa todo o processo de criação e, no caso de Neves, é amplificado pelo uso não convencional desses procedimentos. O estabelecimento de vínculos entre obras, autor e contexto de produção tem como objetivo detectar nexos e recorrências entre os trabalhos de Neves, em suas diversas etapas de desenvolvimento, e questões pertinentes acerca das artes visuais contemporâneas. O tratamento acadêmico do material, feito sob a perspectiva da crítica de processos de acordo com contribuições teóricas de Cecilia Almeida Salles, faz emergir discussões sobre os tempos e espaços fotográficos, autoria, memória e arquivos. Ao lado de Salles aparecem autores que colaboram para uma abordagem interdisciplinar: Vincent Colapietro, Henri Bergson, Edgar Morin, Georges Didi-Huberman, Jacques Rancière e Michel FoucaultThis research has as its starting point the access to the studio and the creation archives of the Brazilian artist Eustáquio Neves. The investigation of the paths identified in Neves' s works, sketches, notes and speeches, seeks to establish relations between the creation processes and the communicating presence materialized in the artist's works, in order to discover how the procedures adopted by the author transform images into manifestos that carry memories deliberately evoked, as they populate a fictional universe within their own times and spaces. Neves places photography in the context of the visual arts by creating complex images in which the process reminiscences - both photographic and extra-photographic - impose themselves, as well as the political statement. Presence therefore results from a semantic investment that permeates the entire creation process and, in the case of Neves, is amplified by the unconventional use of these procedures. The establishment of links between works, author and context of production aims to detect nexuses and recurrences between the material, in its various stages of development, and pertinent questions about contemporary visual arts. The academic treatment is made from the perspective of process criticism in accordance with Cecilia Salles' theoretical contributions and gives rise to discussions about photographic times and spaces, authorship, memory and archives. Alongside Salles are authors who collaborate for an interdisciplinary approach: Vincent Colapietro, Henri Bergson, Edgar Morin, Georges Didi-Huberman, Jacques Rancière and Michel FoucaultConselho Nacional de Pesquisa e Desenvolvimento Científico e Tecnológico - CNP
Pensando sobre políticas públicas de lazer para juventudes em contextos de vulnerabilidade social: contribuições a partir de pesquisa em Ribeirão das Neves
No full textPensando sobre políticas públicas de lazer para juventudes em contextos de vulnerabilidade social: contribuições a partir de pesquisa em Ribeirão das Neves – Minas Gerais / Vânia Noronha (org.). - Belo Horizonte: Editora, 2009. 176 p. : il.Esta publicação é resultado de um convênio estabelecido entre a Sociedade Mineira de Cultura, com interveniência da Pontifícia Universidade Católica de Minas Gerais (PUC Minas), de Belo Horizonte. O Projeto foi executado pelo curso de Educação Física, em parceria com a Pró-Reitoria de Extensão, por meio do Instituto da Criança e do Adolescente e do Programa de Pós-Graduação em Geografia. No período de janeiro de 2008 a janeiro de 2009, foi realizada uma pesquisa na cidade de Ribeirão das Neves com o objetivo de elaborar e aplicar um diagnóstico sociopopulacional e cultural (esporte e lazer) para a cidade, visando construir subsídios para o desenvolvimento de políticas de inclusão pelo esporte e lazer de jovens sujeitos à situação de risco para a violência.Rede CEDES / M
Neohygrocybe fumosa J. S. Cardoso, M. A. Neves & J. S. Oliveira 2023, sp. nov.
No full text<i>Neohygrocybe fumosa</i> J.S. Cardoso, M.A. Neves & J.S. Oliveira, <i>sp. nov.</i> (Figs. 3f–h, 4d–f, 5) <p>MycoBank # MB844323</p> <p>Etymology:—From Latin “fumosus” = smoky, grey, changing to brown; refers to the greyish light brown pileus.</p> <p> Type:— BRAZIL. Mato Grosso: Novo Mundo, Reserva Particular do Patrimônio Natural Cristalino, Castanheira Trail, 250 m elev., 9º33’52’’S 55º54’19’’W, 9 January 2019, <i>Cardoso, J. S. & Furtado, A. N. M.</i> 600 (FLOR67460, holotype).</p> <p> Diagnosis:—Basidiomata dull-coloured, pileus umbonate, greyish brown, lamellae pale greyish brown, stipe light silvery grey, basidiomata with a distinct nitrous smell and without colour changes when injured. Differs from <i>Neohygrocybe subovina</i> by having brighter colours, no colour changes upon bruising, ellipsoid basidiospores and pyriform cheilocystidia.</p> <p> Description:— <i>Pileus</i> 30–44 mm diam., plane-convex, umbonate, sometimes tearing in the centre, slightly fibrillose, moist to dry, becoming translucent-striate towards margin, hygrophanous, light grey-brown (oac730, oac729) to brown (oac748, oac749); margin translucent-striate, uplifted to revolute, undulating, eroded, pale grey (oac732). <i>Lamellae</i> uncinate, up to 8mm broad, subdistant, thick, white with shades of grey-brown (oac711, oac718), intervenose, with veins projecting in the lamellar faces; lamellulae of two lengths, anastomosing. <i>Stipe</i> 75–83 × 5–7 mm, central, flexuous, hollow, smooth, glabrous, moist to dry, silky, tapering towards the base, light silvery grey (oac774, oac690) to whitish. <i>Odour</i> nitrous.</p> <p> <i>Basidiospores</i> 6.8– <i>7.99</i> –9.1 × 5.2– <i>6.08</i> –7.1 µm, Q = 1.315, ellipsoid, smooth, hyaline, inamyloid, thin-walled, guttulate, hilar appendage visible. <i>Basidia</i> 26.8–36.4 × 6.3–9.7 (–10.8) µm, clavate, thin-walled, hyaline, 2–4-spored, sterigmata up to 7 µm, with basal regular clamp connections. <i>Lamellar edge</i> fertile. <i>Cheilocystidia</i> 32.8–35.6 × 16.6– 22.1 µm, pyriform, like a swollen basidiole, sometimes guttulate. <i>Pleurocystidia</i> absent. <i>Pseudocystidia</i> 96.7–219.3 × 15.1–23.6 µm, obclavate to ventricose-rostrate, apex sometimes with conspicuous cellular contents, emerging from the lamellar trama and projecting up to 40 µm above basidia and basidioles (Figure 5). <i>Lamellar trama</i> regular, composed of parallel inflated elements, 40.2–233.2 × 8.6–33.8 µm, clamp connections present. <i>Pileipellis</i> a cutis, with parallel, undifferentiated hyphae, 3.3–7 µm diam., some with granular encrusting pigments, pale brownish in water, hyaline in KOH, clamp connections present. <i>Stipitipellis</i> a cutis, hyphae 2.3–15.9 µm diam., hyaline in KOH and water, with rare encrustations, clamp connections present.</p> <p> Specimens examined:— BRAZIL. Mato Grosso: Alta Floresta, RPPN Cristalino, Dr. Haffer’s Trail, 250 m elev., 9º3”10’ S 55 º54”53’ W, 25 January 2018, <i>Cardoso, J. S</i> <i>.</i> 277 (FLOR63574); Novo Mundo, RPPN Cristalino, Castanheira Trail, 250 m elev., 9º33’52’’S 55º54’19’’W, 9 January 2019, <i>Cardoso, J. S</i> <i>. & Furtado, A. N. M.</i> 600 (FLOR67460).</p> <p>Distribution:—Known only from the type locality.</p> <p> Habitat:—Growing solitary on clay soils of <i>terra-firme</i> forest.</p> <p> Comments:— <i>Neohygrocybe fumosa</i> is the first species of the genus described from Brazil. There are two species known from the neotropical region: <i>Neohygrocybe subovina</i> (Hesler & A.H. Sm.) Lodge & Padamsee (2013 [2014]: 41) and <i>Hygrocybe ovinoides</i> Lodge, S.A. Cantrell & T.J. Baroni (2004: 1312) combined in <i>Neohygrocybe</i> herein. <i>Neohygrocybe subovina</i>, from USA, also has cheilocystidia and pseudocystidia projecting from the hymenium, but the basidiomata are much darker in colour, the lamellae bruise pink to reddish brown or darker, the basidiospores are globose to subglobose rather than ellipsoid, and the cheilocystidia are vermiform and cylindrical rather than pyriform (Hesler & Smith 1963). <i>Hygrocybe ovinoides</i> produces very small basidiomata which are also dark in colour, but the pilei have a white margin (Cantrell & Lodge 2004). In the microscopy, <i>H. ovinoides</i> lacks cheilocystidia and has hook-like pileocystidia (Cantrell & Lodge 2004). Both <i>N. subovina</i> and <i>H. ovinoides</i> lack the nitrous odour found in <i>N. fumosa.</i></p>Published as part of <i>Cardoso, Juli Simon, Moncalvo, Jean-Marc, Lodge, D. Jean, Margaritescu, Simona, Neves, Maria Alice & Oliveira, Jadson J. S., 2023, Studies in Hygrocybe s. l. (Hygrocyboideae, Hygrophoraceae) in Brazil: New species of Humidicutis and Neohygrocybe, pp. 57-71 in Phytotaxa 607 (1)</i> on pages 64-66, DOI: 10.11646/phytotaxa.607.1.5, <a href="http://zenodo.org/record/8212211">http://zenodo.org/record/8212211</a>
Setacheres eudistomus Johnsson, Bahia & Neves, 2016, sp. nov.
No full textSetacheres eudistomus sp. nov. (Figs. 2–4) Material examined. Holotype female (UFBA 1722) and two paratype females (UFBA 1723); (UFBA 1724), Porto da Barra Beach (13 °0'14.01"S, 38 ° 32 '3.14"W), Salvador city, Bahia State, Brazil, collected by C. Bahia and V. Queiroz on 10 December 2012. All specimens were found attached externally on the tunic of Eudistoma vannamei. Paratype (UFBA 1723) dissected and mounted on slide. Remaining types preserved in alcohol. Description of female. Mean body length (excluding caudal setae) 740 µm (736–744 µm) and mean body width 431 µm (428–434 µm) (n = 3). Body (Fig. 2 A) cyclopiform, dorsoventrally flattened, prosome longer than wide, and urosome cylindrical. Pedigerous somite 1 completely fused to cephalosome to form cephalothorax. Pedigerous somites 2–4 with lateral posterior margins rounded. Pedigerous somite 3 more curved, longer than pedigerous somite 2 and partly covering pedigerous somite 4. Pedigerous somite 4 smaller than third somite and slightly larger than fifth somite. Prosome 511 µm long and 431 µm width. Length: width ratio = 1.2: 1. Urosome (Fig. 2 B) 4 -segmented. Fifth pedigerous somite 43 µm long and 113 µm width. Genital double-somite 86 µm long, maximum width 102 µm, length: width ratio = 0.8: 1. Vestigial leg 6 mid-laterally located, close to spinule; row of setules along posterolateral margins and two tooth-like projections close to genital openings. Two postgenital somites, both wider than long (36 × 59, 36 × 54 µm, respectively), lateral margins naked; epimera postero-laterally pointed. Ventral surface of anal somite covered by spinules. Prosome: urosome ratio = 2.5: 1. Caudal rami (Fig. 2 B) slightly longer than wide, 27 × 25 µm with spinules along inner margin, with six setae (seta I absent); setae VI and VII naked and setae IV and V plumose. Posterior margin with rounded projection between setae III and IV. Length of setae II–VII 45, 125, 186, 245, 80 and 42 µm, respectively. Rostrum (Fig. 2 C) large, wider than long (234 × 145 µm), triangular with rounded apex. Antennule (Fig. 2 D) 300 µm long (not including setae), 21 -segmented. Length of segments: 34, 17, 8, 8, 11, 5, 11, 7, 11, 4, 13, 13, 19, 20, 17, 20, 24, 27, 12, 13 and 6 µm, respectively. Segmental homologies and armature as follows: 1 (I)- 2; 2 (II)- 2; 3 (III)- 2; 4 (IV)- 2; 5 (V)- 2; 6 (VI)- 2; 7 (VII)- 2; 8 (VIII)- 2; 9 (IX–XII)- 6; 10 (XIII)- 2; 11 (XIV)- 2; 12 (XV)- 2; 13 (XVI)- 2; 14 (XVII)- 2; 15 (XVIII)- 2; 16 (XIX)- 2; 17 (XX)- 2; 18 (XXI)- 2 + aesthetasc; 19 (XXII–XXIII)- 2; 20 (XXIV–XXV)- 2; 21 (XXVI–XXVIII)- 6. Aesthetasc 64 Μm long. First segment with both setae plumose at distal half. Segments 9-11 with distal tooth-like projection. Antenna (Fig. 3 A) 211 µm long (including distal claw); coxa 25 µm long, with small seta along outer margin; basis 54 µm long, with sparse spinules along inner margin and setules along outer margin. Exopod 1 -segmented, 11 µm long, with two apical setae and small lateral seta; all setae naked. Endopod 3 -segmented; first segment 59 µm long, unarmed; second segment 9 µm long, armed with naked seta; third segment 12 µm long, armed with two distal setae, small seta proximally and distal claw (52 µm long). Oral cone (Fig. 3 B) 162 × 61 µm (long × width), reaching to point between bases of maxillipeds and leg 1. Mandible (Fig. 3 C) with 2 -segmented palp; both segments slender and naked, measuring 18 and 13 µm long, respectively; second segment with two distal setae, smallest seta spinulated and half the length of longer one which is unilaterally spinulated. Mandibular stylet 122 µm long, proximally stout, tapering distally with ten subterminal teeth. Maxillule (Fig. 3 D) bilobed; inner lobe 36 µm long, with five distal setae, one of them smaller and more slender than the others; three of the remaining setae unilaterally plumose; inner margin of inner lobe with setules proximally and bunch of setules distally; outer margin with set of spinules. Outer lobe 13 µm long, armed with four distal setae, two being plumose; outer margin with few spinules. Maxilla (Fig. 3 E) 250 µm long, consisting of syncoxa (100 µm long, with tubular extension of maxillary gland opening) and strongly distally curved claw with naked seta near inner subdistal margin. Maxilliped (Fig. 2 F) 5 -segmented, 267 µm long; syncoxa 82 µm long, with setules along outer margin; basis 84 µm long, with row of setules and few setules along inner and outer margins, respectively. Endopod 3 - segmented, segments measuring 8, 11 and 21 µm, respectively; first segment naked; second one with distal toothlike projection and two naked setae; third segment with serrated spine and distal curved claw-like element, 61 µm long. Legs 1–4 (Fig. 4 A −D) biramous, with 3 -segmented rami. Armature formula as follows: Leg 1 with setules along outer margin of exopod and endopod; proximal exopod segment with large outer spine and without inner seta; middle exopod segment with small outer spine. Legs 2–4 with spinules and setules along outer margins of exopods and endopods, respectively. Leg 5 (Fig. 4 E) with three distal setae, with spinules and setules along outer and inner margins, respectively. Intercoxal plate of leg 1 covered with setules, intercoxal plates of remaining legs totally naked. Male. Unknown. Type locality. Porto da Barra Beach (13 °0'14.01"S, 38 ° 32 '3.14"W), Salvador city, Bahia State, Brazil. Etymology. The specific name “ eudistomus ” refers to the ascidian host of the new species. Remarks. Among the species belonging to the new genus Setacheres it is recognizable the presence of one to three segments posteriorly to the ancestral antennulary segment XXI indicating their degree of fusion (Johnsson 1998, Brian 1927, Johnsson et al. 2001, Johnsson 2002). Setacheres eudistomus sp. nov. shows, as observed in S. lunatus and S. paraboecki, 3 segments posterior to the ancestral XXI (Johnsson 1998). However, in S. paraboecki the ancestral segments IX-XIII are fused and therefore show a total of 20 segments while S. lunatus and the new species share the fusion of articles IX-XII resulting in a 21 -segmented antennule. Setacheres eudistomus sp. nov. differs from S. lunatus in its having of 5 setae on the inner maxillulary lobe, instead of 4 in the latter species and a 5 -segmented maxilliped vs. a 6 -segmented one in S. lunatus (Johnsson 1998). The new species shows the first exopodal segment of leg 1 without an inner seta (I-0) while all other species of the new genus shows the regular setation pattern with an inner seta (I- 1). Distribution. The nine species of Setacheres gen. nov. are recorded exclusively from the Atlantic Ocean. Setacheres ventricosus is known from the Aegean Sea, an embayment of the Mediterranean Sea. The remaining eight species have been recorded exclusively from the western Atlantic; most of them are so far restricted to the Brazilian coast. Setacheres picinguabensis is known to occur in São Paulo State, Warm Temperate Southwestern Atlantic province (WTSA) and S. abrolhensis in Bahia State (Johnsson & Neves 2012), Tropical Southwestern Atlantic province (TSA) (Spalding et al. 2007). Three species, S. lunatus, S. aplysinus and S. spinopaulus are restricted to the northeastern coast, occurring in Bahia, Pernambuco and Alagoas States (Johnsson & Neves 2012), all in TSA (Spalding et al. 2007). Setacheres paraboecki and S. unicus are the only species recorded in Rio de Janeiro and Bahia States and São Paulo and Alagoas, respectively and therefore occur in both WTSA and TSA provinces. As S. paraboecki is also recorded from Cuba (Varela 2012), this species ranges in two distinct biogeographic realms, the Tropical Atlantic and the Temperate South America, thus suggesting a wide distributional range than that known in other species as S. unicus. So far, the remaining six species appear to be restricted to the TSA province. These data corroborate the distributional similarity found in other organisms as stony corals, decapods, mollusks and polycladids (Neves et al. 2006, Neves et al. 2008, Neves et al. 2010, Queiroz et al. 2011, Queiroz et al. 2013, Sales et al. 2011).Published as part of Johnsson, Rodrigo, Bahia, Cristiano & Neves, Elizabeth, 2016, A new genus of Asterocheridae (Copepoda: Siphonostomatoida) ectoassociate of the ascidian Eudistoma vannamei Millar, 1977 (Polycitoridae) from Brazil, pp. 162-170 in Zootaxa 4114 (2) on pages 165-168, DOI: 10.11646/zootaxa.4114.2.5, http://zenodo.org/record/26557
Obidosus carnaval Osvaldo Villarreal & Ludson Neves de Ázara & Kury 2019
No full textObidosus carnaval (Villarreal-Manzanilla and Pinto-da-Rocha, 2006) newcombination (Figure 9 (i,j)) Protimesius carnaval Villarreal-Manzanilla and Pinto-da-Rocha 2006: 229, figs 29 – 35, 44 – 45. Type data ³ holotype (MZSP 24154); 1 ♀ paratype (MZSP 24154), 7 ♀ paratypes (MZSP 24153), BRAZIL, Acre, Parque Nacional da Serra do Divisor, Rio Moa, Amazonian Rain Forest (7°39´S, 72°41´W). 2 ♀ paratypes (MZSP 19227), Parque Nacional da Serra do Divisor, 22.XI. – 12.I.2000; 1 ³ 1 ♀ paratypes (MNRJ HS 684), COLOMBIA, Amazonas, 6 km N Letícia.Published as part of Osvaldo Villarreal, Ludson Neves de Ázara & Kury, Adriano Brilhante, 2019, Revalidation of Obidosus Roewerı 1913 and description of two new cave-dwelling species of Protimesius Roewerı 1913 from Brazil (Opiliones: Stygnidae), pp. 965-989 in Journal of Natural History 53 (15) on page 982, DOI: 10.1080/00222933.2019.1620893, http://zenodo.org/record/367322
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