154,437 research outputs found
Mycetophila tonnoiri Oliveira & Amorim 2012
No full texttonnoiri Oliveira & Amorim, 2012: 15, 7 (fig. 9, wing), 16 (fig. 20, male terminalia). Type locality: Colombia, Magdalena, Parque Nacional Natural Santa Marta, San Lorenzo. HT M (IAvH). Distr.: Colombia (Magdalena).Published as part of Oliveira, Sarah Siqueira & Amorim, Dalton De Souza, 2016, FAMILY MYCETOPHILIDAE, pp. 65-72 in Zootaxa 4122 (1) on page 68, DOI: 10.11646/zootaxa.4122.1.13, http://zenodo.org/record/26433
Docosia adusta Oliveira & Amorim 2011
No full text<p> <b>adusta</b> Oliveira & Amorim, 2011: 689, 690. (fig. 1, habitus), 691 (fig. 2, thorax), 692 (fig. 3, asa), 693 (figs. 4-6, M terminalia), 694 (fig. 7, F terminalia). Type locality: Colombia Cundinamarca, Parque Nacional Natural Chingaza Alto de La Bandera. HT M (IAvH). Distr.: Colombia (Cundinamarca).</p>Published as part of <i>Oliveira, Sarah Siqueira & Amorim, Dalton De Souza, 2016, FAMILY MYCETOPHILIDAE, pp. 65-72 in Zootaxa 4122 (1)</i> on page 67, DOI: 10.11646/zootaxa.4122.1.13, <a href="http://zenodo.org/record/264337">http://zenodo.org/record/264337</a>
Docosia fumosa Oliveira & Amorim 2012
No full textfumosa Oliveira & Amorim, 2012: 6, 5 (fig. 1, habitus), 7 (figs. 5-6, wings), 11 (fig. 16, male terminalia), 13 (fig. 17, female terminalia). Type locality: Ecuador, Pichincha, E. Papallacta (Quito/Baeza). HT M (MZUSP). Distr.: Colombia (Huilla), Ecuador (Pichincha).Published as part of Oliveira, Sarah Siqueira & Amorim, Dalton De Souza, 2016, FAMILY MYCETOPHILIDAE, pp. 65-72 in Zootaxa 4122 (1) on page 68, DOI: 10.11646/zootaxa.4122.1.13, http://zenodo.org/record/26433
Paraleia bolivari Oliveira & Amorim 2012
No full textbolivari Oliveira & Amorim, 2012: 4, 6 (fig. 2, thorax), 7 (figs. 3–4, wings), 8 (fig. 13, male terminalia), 9 (fig. 14, female terminalia), 10 (fig. 15, female terminalia). Type locality: Colombia, Cundinamarca, Parque Nacional Natural Chingaza. HT M (IAvH). Distr.: Colombia (Cundinamarca).Published as part of Oliveira, Sarah Siqueira & Amorim, Dalton De Souza, 2016, FAMILY MYCETOPHILIDAE, pp. 65-72 in Zootaxa 4122 (1) on page 68, DOI: 10.11646/zootaxa.4122.1.13, http://zenodo.org/record/26433
Phronia denticulata Oliveira & Amorim 2012
No full textdenticulata Oliveira & Amorim, 2012: 12, 7 (figs. 7–8, wings), 14 (fig. 18, male terminalia), 15 (fig. 19, female terminalia). Type locality: Colombia, Cundinamarca, Parque Nacional Natural Sumapaz Bocatoma, Cerro El Zapato. HT M (IAvH). Distr.: Colombia (Cundinamarca).Published as part of Oliveira, Sarah Siqueira & Amorim, Dalton De Souza, 2016, FAMILY MYCETOPHILIDAE, pp. 65-72 in Zootaxa 4122 (1) on page 68, DOI: 10.11646/zootaxa.4122.1.13, http://zenodo.org/record/26433
Marasmius rubicundus J. S. Oliveira 2022, stat. nov.
No full textMarasmius rubicundus (Singer) J.S. Oliveira, stat. nov. (Figs 15B; 18) Marasmius haematocephalus var. rubicundus Singer, Sydowia 18: 337 (Singer 1965). — Type: Bolivia. La Paz, Nor-Yungas, Charobamba, 1300 m a.s.l., 30.I.1956, Singer B 743 (LIL), holotype; Singer B 737 (LIL); Coroico, 1700 m a.s.l., 7.II.1956, Singer B 945 (LIL); Beni, Vaca Diez, Guayaranerin, 4.III.1956, Singer B 1963 (LIL); Singer B 1755 (LIL). EPITYPE. — Brazil. São Paulo State, São Paulo City, Parque Estadual da Cantareira, Núcleo Engordador, 30.I.2012, J.J.S. Oliveira & V. Motato-Vásquez JO464 (epi-, designated here, SP[SP 445549]!), nrITS (ON502658) and nrLSU (ON502728). ADDITIONAL EXAMINED MATERIAL. — Brazil. São Paulo State, Santo André City, Reserva Biológica de Paranapiacaba, 16.XII.2009, M. Capelari & L.A.S. Ramos 4567 (SP[SP 445931]!); M. Capelari & L.A.S. Ramos 4570 (SP[SP 446073]!); 14.I.2010, J.J.S. Oliveira & M. Capelari JO1 (SP[SP 446075]!); 16.III.2010, J.J.S. Oliveira JO43 (SP[SP 446069]!); 15.X.2010, J.J.S. Oliveira & C.L.A. Pires JO223 (SP[SP 446074]!); 16.X.2010, J.J.S. Oliveira & C.L.A. Pires JO228 (SP[SP 445448]!); J.J.S. Oliveira & C.L.A. Pires JO230 (SP[SP 446076]!); 17.X.2010, J.J.S. Oliveira & C.L.A. Pires JO245 (SP[SP 446046]!); J.J.S. Oliveira & C.L.A. Pires JO246 (SP[SP 445454]!); 5.XI.2010, J.J.S. Oliveira JO261 (SP[SP 446051]!); 7.XI.2010, J.J.S. Oliveira & A.V. Costa JO275 (SP[SP 446059]!); 7.XII.2010, J.J.S. Oliveira, P.O. Ventura & A.V. Costa JO281 (SP[SP 445464]!); J.J.S. Oliveira, P.O. Ventura & A.V. Costa JO283 (SP[SP 446061]!); J.J.S. Oliveira, P.O. Ventura & A.V. Costa JO295 (SP[SP 446063]!); J.J.S. Oliveira, P.O. Ventura & A.V. Costa JO296 (SP[SP 445476]!); 9.XII.2010, J.J.S. Oliveira, P.O Ventura & A.V. Costa JO316 (SP[SP 445488]!); J.J.S. Oliveira, P.O. Ventura & A.V. Costa JO318 (SP[SP 446048]!); J.J.S. Oliveira, P.O. Ventura & A.V. Costa JO319 (SP[SP 446047]!); São Paulo City, Parque Estadual das Fontes do Ipiranga, 1.III.2011, J.J.S. Oliveira & F. Karstedt JO330 (SP[SP 446065]!); J.J.S. Oliveira & F. Karstedt JO335 (SP[SP446067]!); J.J.S. Oliveira & F.Karstedt JO338 (SP[SP 446066]!); 18.X.2011, J.J.S. Oliveira & P.O.Ventura JO380 (SP[SP 446064]!); São Paulo City, Parque Estadual da Cantareira, Núcleo Engordador, 19.XII.2011, J.J.S. Oliveira & M. Capelari JO445 (SP[SP 445537]!); J.J.S. Oliveira & M. Capelari JO446 (SP[SP 446054]!); J.J.S. Oliveira & M. Capelari JO447 (SP[SP 446053]!); 9.II.2012, J.J.S. Oliveira & M. Capelari JO481 (SP[SP 446043]!); J.J.S. Oliveira & M. Capelari JO482 (SP[SP 446055]!); J.J.S. Oliveira & M. Capelari JO483 (SP[SP 445560]!); 16.II.2012, J.J.S. Oliveira & M. Capelari JO492 (SP[SP 446045]!); J.J.S. Oliveira & M. Capelari JO514 (SP[SP 446071]!); J.J.S. Oliveira & M. Capelari JO516 (SP[SP 446057]!); Iporanga City, Parque Estadual Turístico do Alto Ribeira, Núcleo Santana, 29.II.2012, J.J.S. Oliveira & D.E. Desjardin JO529 (SP[SP 445577]!); D.E. Desjardin DED8675 (SP[SP 445665]!); Lageado, 29.II.2012, J.J.S. Oliveira & D.E. Desjardin JO534 (SP[SP 446077]!). MYCOBANK. — MB 842539. HABIT AND SUBSTRATE. — Marasmioid (Figs 15A; 18A), solitary to gregarious, on dried eudicotyledonous leaves and sticks in the forest litter. DISTRIBUTION. — Originally from La Paz and Beni, Bolivia, as M. haematocephalus var. rubicundus (Singer 1965, 1976), it is now known from Southeastern Brazil. DESCRIPTION Pileus (Figs 15A; 18A) 2.5-20.5 mm diam., conical, hemispherical to convex, sulcate, center flat to umbonate, smooth or somewhat wrinkled, margin decurved to almost straight, edge entire to crenate; sometimes pale pinkish beige or salmon color (N 10 Y 20 M 40 to N 10 Y 30 M 50), often “Canna” pink or rose (N 20 Y 00-20 M 40-60), tending to very pale pinkish lilac (N 20 Y 20 M 60), then vibrant or ruby pink (N 40 Y 50 M 80), pinkish red (N 20 Y 50 M 70, N 20 Y 60 M 70 to N 20 Y 70 M70), or pinkish brown “Egyptian red” (N 40 Y 50- 60 M 60), sometimes pink with a slight hue of yellow (N 30 Y 50 M 50), or many times pale red or “Carnelian” (N 60 Y 40-60 M 90-99), light reddish brown (N 50-60 Y 90-99 M 90), with center darker red (N 70 Y 60 M 99) or pinkish brown (N 50 Y 70 M 70), or dark lilac (N 70 Y 00 M 99) or dark pink (N 70 Y 40 M 90); membranous, context thin (<1 mm); glabrous, dry, dull, papyraceus to subvelutinous, non-hygrophanous. Lamellae (Figs 15A; 18A) Free, adnexed, or sinuate to narrowly adnate, distant to subdistant, L = 7-12, equal, narrow to broad, straight, cultriform to ventricose, simple, l = 0 (-1), dull, smooth, white to cream (N 00 Y 10 M 00), or whitish pink (N 00 Y 10 M 10 or N 00 Y 40 M 10-20), edges even, non-marginate, interlamellar hymenium concolorous with the lamellae faces or partly concolorous with the pileus. Stipe (Figs 15A; 18A) 8-63 × 0.3-0.8 mm, central, filiform, thin, equal, sometimes with broader base, with circular caliber, compressed when dried, chitinous, hollow; apex pale pink (N 00 Y 10 M 10 or N 30 Y 50 M 80) becoming bronze brown (N 40 Y 60 M 50 to N 80 Y 70 M 40) to dark brown (N 80 Y 99 M 30), or almost black at the base, glabrous, smooth, with a silky bright; with a scarce, white, tomentose basal mycelium. Odor Not distinctive. Basidiospores (Fig. 18B) (15.4-)16.2-21.7(-22)×2.7-4.7(-5) µm (xrm = 18-19.7 × 3.5-4 µm; xmm = 19 [± 0.5] × 3.8 [± 0.2] µm; Qrm = 4.6- 5.5; Qmm = 5 [± 0.3]; n / s = 30/28), exceptional spore size of JO316 with 18.3-23.9 × 3.1-4.8 µm (xm = 21.3 [± 1.3] × 3.9 [± 0.4] µm; Qm = 5.4 [± 0.6]; n / s = 30/1), oblong, clavate to subfusoid, smooth, hyaline, thin-walled, inamyloid. Basidia (Fig. 18C) 21.3-36.3 × 6-7.5 µm, clavate, smooth, hyaline to slightly fuscous, thin-walled, 4-sterigmate, inamyloid. Basidioles (Fig. 18D) 22-28.8 × 5.6-8.8 µm, clavate, sometimes as cystidioles, smooth, hyaline to slightly fuscous, inamyloid. Pleurocystidia (Fig. 18E) (19.5-)25.6-71.7 × 5-12.3 µm, broadly clavate, capitate, almost mucronate or acuminate, with a conical apex, or ampullaceous, or occasionally with apical, serial, slight constrictions, ending with a capitule, smooth, slightly fuscous, thin-walled, refractive, inamyloid, abundant. Cheilocystidia (Fig. 18F) Similar to the Siccus-type broom cells of the pileipellis; main body 11.3-20 × 5.6-10.6 µm, clavate to slightly turbinate, wall somewhat thick, hyaline; setulae more strictly apical, rarely somewhat divergent, erect, 2-7.5 × 0.5-1 µm, cylindrical, digitiform or needle-like, simple, solid, hyaline to pale brown, regular in outline, apex obtuse to slightly acute. Lamellar trama Dextrinoid, irregular, interwoven, hyphae cylindrical, 1.5-10 µm diam., regular in outline,branched, hyaline, thin-walled,smooth. Pileus trama Dextrinoid, similar to the lamellar trama, hyphae 2-10 µm diam. Pileipellis Hymeniform, composed of Siccus-type broom cells (Fig.18G), abundant, brown when grouped, bleaching in KOH solution; main body 7.5-20 × 6.3-11.3 µm, clavate, turbinate, sometimes branched, ventricose to irregular in outline, hyaline, thin-walled to slightly thick-walled, weakly dextrinoid; setulae apical, erect, 2-7.5 × 0.6-1 µm, cylindrical, digitiform or needle-like, simple, regular in outline, or slightly contorted, solid, hyaline to pale brown, apex obtuse to slightly acute. Stipe trama Dextrinoid especially the internal hyphae and those of the stipe apex, cortical hyphae parallel, cylindrical, regular in outline, 3.8-8 µm diam., smooth, dark chestnut brown, yellowish brown when separated, thick-walled; internal hyphae regular in outline, 2.5-6.5 µm diam., parallel. Clamp connections Present in all tissues, except in the cortical hyphae of the stipe. REMARKS The type collections were not examined in the present study as we had no reply from LIL herbarium in this pandemic time. However, Singer (1965, 1976) provided enough morphological data to unambiguously determine the examined specimens from São Paulo as authentic representatives of M. haematocephalus var. rubicundus. The pigmentation and size of the pileus, the number of lamellae, and the size of the basidiospores (15-21 × 4-4.8 µm in Singer [1976]) match the examined material. Marasmius rubicundus is 0.7-0.9 % (nrITS) and 0.5-0.7 % (nrLSU) dissimilar to M. haematocephalus, but cladogenesis reveals vicariance in sympatry. In the phylogenetic trees (Figs 1; 3) of nrITS, M. rubicundus (Singer) J.S. Oliveira, stat. nov., M. auranticapitatus J.S. Oliveira, sp. nov., and M. haematocephalus are embedded within haemat_cp2a. In multilocus analyses, nrITS + nrLSU (Fig. 4) and nrITS + rpb 2 + ef 1 - α (Fig. 5), three species were resolved within this complex: M. rubicundus (Singer) J.S. Oliveira, stat. nov. sister to M. auranticapitatus J.S. Oliveira, sp. nov. with high support, and paraphyletic to M. haematocephalus. Morphologically, M. rubicundus (Singer) J.S. Oliveira, stat. nov. is very similar to M. haematocephalus, only more conspicuously distinct by having a lighter pileus pigmentation and slightly smaller basidiospores (x mm = 18.9 [± 0.5] × 3.8 [± 0.1] µm, Qmm = 5 [± 0.2] vs xmm = 20.5 [± 0.3] × 3.9 [± 0.2] µm, Qmm = 5.2 [± 0.1]). Marasmius haematocephalus s. str. regards the “ rubro -sanguineo ” of its protologue as deep or dark blood red or vinaceous (Singer 1958). In fact, the separation of M. rubicundus (Singer) J.S. Oliveira, stat. nov. and M. haematocephalus is very narrow in a broad sense, as they are nearly identical in other morphological characteristics. The species divergence is only evident in multilocus phylogenetic analyses where M. rubicundus (Singer) J.S. Oliveira, stat. nov. is rather closer to M. auranticapitatus J.S. Oliveira, sp. nov. (Figs 4; 5). The exceptional spore sizes of JO316, possibly a hybrid, strenghtens the plausibility of the most recent common ancestor between them. Although speciation is demonstrated, this ancestry trace or possible partial intercompatibility and gene flow are elements of a recent divergence. The strain JO316 seems in a transitional/ intermediate position (Fig. 4) along with other strains of M. rubicundus (Singer) J.S. Oliveira, stat. nov., but the basidiospores are more compatible with M. auranticapitatus J.S. Oliveira, sp. nov.. JO316 and JO226 highlights the powerful phylogenetic signal of spore sizes, an evident correlation between this characteristic and the genotype behind the species concepts. The pale red pileus in M. rubicundus (Singer) J.S. Oliveira, stat. nov. is consistent with M. pallescens, but this later has shorter (11-17 µm) basidiospores (Singer 1976). For more color pictures showing variation of pileus pigmentation of M. rubicundus (Singer) J.S. Oliveira, stat. nov., see Appendix (Figs S7-S 11). It is not similar to any of the heterotypic synonyms of M. haematocephalus listed in Singer (1976) but M. rhodocephalus Fr. (Fries 1851; Appendix) with type presumed lost but connection is not sharp.Published as part of S, Jadson José, Oliveira, ouza de, Capelari, Marina, Margaritescu, Simona & Moncalvo, Jean-Marc, 2022, Disentangling cryptic species in the Marasmius haematocephalus (Mont.) Fr. and M. siccus (Schwein.) Fr. species complexes (Agaricales, Basidiomycota), pp. 91-137 in Cryptogamie, Mycologie 20 (5) on pages 120-124, DOI: 10.5252/cryptogamie-mycologie2022v43a5, http://zenodo.org/record/782935
Ponto de Vista, Cláudio Márcio Oliveira.
No full textPonto de vista do professor Cláudio Márcio Oliveira sobre o tema "Do ponto de vista da pratica cotidiana da Educação Física, quais as metodologias de ensino predominantes e seus referenciais teóricos subjacentes?"
Eudendrium caraiuru Marques & Oliveira 2003
No full text<i>Eudendrium caraiuru</i> Marques & Oliveira, 2003 <p> Synonyms in the area: <i>Eudendrium glomeratum</i> —Marques 1993; Rosso & Marques 1997; Oliveira <i>et al.</i> 2000; Marques 2001; Migotto <i>et al.</i> 2001; Silveira & Morandini 2011 [polyp] [non <i>Eudendrium glomeratum</i> Picard, 1951].</p> <p> Remarks: common species on the Brazilian coast (Marques <i>et al.</i> 2006). Further taxonomic details in Marques & Oliveira (2003).</p> <p> Distribution in South America: polyp—Atlantic Ocean, Brazil, from 3°S to 4.50°S, from 22.75°S to 25.58°S, from 38°S to 38.10°S (Marques 1993; Migotto 1996; Rosso & Marques 1997; Oliveira <i>et al.</i> 2000; Marques 2001; Migotto <i>et al.</i> 2001; Marques & Oliveira 2003; Oliveira & Marques 2005; Marques <i>et al.</i> 2006; Shimabukuro & Marques 2006a, abstract; Shimabukuro <i>et al.</i> 2006; Shimabukuro 2007; Silveira & Morandini 2011; Marques <i>et al</i>. 2013; Fernandez <i>et al</i>. 2014, 2015; Miranda <i>et al</i>. 2015).</p> <p> Habitat: polyp—in shallow waters, on fouling, ascidians, bryozoans, barnacles, gastropods, mussels, polychaete tubes, rocks, test panels and other artificial substrates (Migotto <i>et al.</i> 2001; Marques & Oliveira 2003; Marques <i>et al.</i> 2006; Shimabukuro & Marques 2006a; Shimabukuro 2007; Fernandez <i>et al</i>. 2014, 2015).</p>Published as part of <i>OLIVEIRA, OTTO M. P., MIRANDA, THAÍS P., ARAUJO, ENILMA M., AYÓN, PATRICIA, CEDEÑO-POSSO, CRISTINA M., CEPEDA-MERCADO, AMANCAY A., CÓRDOVA, PABLO, CUNHA, AMANDA F., GENZANO, GABRIEL N., HADDAD, MARIA ANGÉLICA, MIANZAN, HERMES W., MIGOTTO, ALVARO E., MIRANDA, LUCÍLIA S., MORANDINI, ANDRÉ C., NAGATA, RENATO M., NASCIMENTO, KARINE B., JÚNIOR, MIODELI NOGUEIRA, PALMA, SERGIO, QUIÑONES, JAVIER, RODRIGUEZ, CAROLINA S., SCARABINO, FABRIZIO, SCHIARITI, AGUSTÍN, STAMPAR, SÉRGIO N., TRONOLONE, VALQUÍRIA B. & MARQUES, ANTONIO C., 2016, Census of Cnidaria (Medusozoa) and Ctenophora from South American marine waters, pp. 1-256 in Zootaxa 4194 (1)</i> on page 58, DOI: 10.11646/zootaxa.4194.1.1, <a href="http://zenodo.org/record/10068449">http://zenodo.org/record/10068449</a>
Multiplicação in vitro de variedades de oliveira "Arbequina" e "Maria da Fé" em diferentes meios de culturas e fitorreguladores
No full textProjeto acadêmico (graduação) - Universidade Federal de Santa Catarina. Campus Curitibanos. Ciências Rurais.A oliveira (Olea europaea L.) pertence à família Oleaceae, sendo cultivada pela sua produção de frutos para a extração do azeite de oliva e azeitonas de mesa, além da sua grande importância econômica, social e cultural. Tem ocorrência principalmente na bacia do mediterrâneo, sendo estendida para vários países do mundo. O Brasil é o segundo maior importador de azeite e o quarto maior importador de azeitonas de mesa. Dessa maneira, o desenvolvimento de pesquisas que promovam melhorias na produção e qualidade dos produtos pertinente, porém ainda são consideradas insuficientes. Como alternativa a essas limitações, o presente trabalho tem como objetivo estabelecer a micropropagação de variedades de oliveira adaptadas no Estado de Santa Catarina e Sul do Brasil. Para tanto, serão utilizadas técnicas que promovam a proliferação de brotações por organogênese direta, para a produção de mudas em grande quantidade. Para iniciação das culturas serão testados diferentes métodos de desinfestação, formulações salinas, diferentes níveis e tipos de fitorreguladores para promover maiores taxas de multiplicação. Antes da aclimatização e adaptação no ambiente serão avaliados diferentes métodos de indução do enraizamento. Esse projeto possibilitará a identificação de técnicas de cultivo para otimizar e reduzir custos, obtendo altas taxas de multiplicação, disponibilidade de mudas certificadas para estimular o cultivo no Brasil e com variedades de alta produtividade para extração do óleo e dos frutos com qualidade
Amblyseius constrictus Argolo, Oliveira & Moraes 2015
No full textAmblyseius constrictus Argolo, Oliveira & Moraes, 2015 Amblyseius constrictus Argolo, Oliveira & Moraes in Argolo et al., 2015: 749. Records in Bahia: Argolo et al., 2015: 749; present study.Published as part of Argolo, Poliane Sá, Vital Santos, Renata M., Leão Bittencourt, Maria A., Da Silva Noronha, Aloyséia C., De Moraes, Gilberto J. & Oliveira, Anibal Ramadan, 2017, Phytoseiid mites (Acari: Phytoseiidae) associated with tropical ornamental plants, with a checklist and a key to the species of Bahia, Brazil, pp. 345-364 in Zootaxa 4258 (4) on page 349, DOI: 10.11646/zootaxa.4258.4.3, http://zenodo.org/record/57010
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