89,604 research outputs found
Triphora charybdis M. R. Fernandes & Pimenta 2015
No full textTriphora charybdis M.R. Fernandes & Pimenta, 2015 Triphora charybdis M.R. Fernandes & Pimenta, 2015b: 507, fig. 7c–k. Type locality. Brazil, 23º10’01”S, 41º03’13”W, 107 m deep, Rio de Janeiro state. Type material. MNRJ 18620, holotype. For a list of paratypes see Fernandes & Pimenta (2015). Distribution. Brazil (Fernandes & Pimenta 2015b; Fernandes & Pimenta 2020), Colombia (Fernandes & Pimenta 2020), Guyana (Fernandes & Pimenta 2020).Published as part of Bakker, Piet A. J. & Albano, Paolo G., 2022, Nomenclator, geographic and stratigraphic distribution of the family Triphoridae (Mollusca: Gastropoda), pp. 1-216 in Zootaxa 5088 (1) on page 45, DOI: 10.11646/zootaxa.5088.1.1, http://zenodo.org/record/583653
R. M. Ro sardo Fernandes, O Thema das Graças na Poesia classica
No full textDelatte A. R. M. Ro sardo Fernandes, O Thema das Graças na Poesia classica. In: L'antiquité classique, Tome 32, fasc. 2, 1963. p. 651
Triphora scylla M. R. Fernandes & Pimenta 2015
No full textTriphora scylla M.R. Fernandes & Pimenta, 2015 Triphora scylla M.R. Fernandes & Pimenta, 2015b: 509, fig. 8. Type locality. Brazil, exit of Guarapari canal, Guarapari, Espírito Santo state. Type material. MZUSP 119013, holotype. IBUFRJ 7568, paratypes. Distribution. Brazil (Fernandes & Pimenta 2015b; Fernandes & Pimenta 2020).Published as part of Bakker, Piet A. J. & Albano, Paolo G., 2022, Nomenclator, geographic and stratigraphic distribution of the family Triphoridae (Mollusca: Gastropoda), pp. 1-216 in Zootaxa 5088 (1) on page 159, DOI: 10.11646/zootaxa.5088.1.1, http://zenodo.org/record/583653
120. Rosados Fernandes (R. M.). Ο Tema das Graças na poesia classica
No full textAubreton Robert. 120. Rosados Fernandes (R. M.). Ο Tema das Graças na poesia classica. In: Revue des Études Grecques, tome 77, fascicule 366-368, Juillet-décembre 1964. pp. 595-598
Contribution of the radical-complex mechanism to the rate of the reaction CH3 + O-2 (+ M) -> CH3O2 (+ M) at high pressures.
No full textEarlier experimental studies of the falloff curves of the reaction CH3 + O-2 M) -> CH3O2 ( M) in the bath gases M = Ar and N-2 (Fernandes et al., J. Phys. Chem. A 2006, 110, 4442), in addition to the usual behavior of the energy-transfer (ET) mechanism, showed first evidence for a participation of the radicalcomplex (RC) mechanism in the reaction at pressures above about 300 bar and at temperatures below 400 K. By extending these measurements to the bath gas M = CO2, more pronounced deviations from the ET mechanism were now observed. This unambiguously confirms the presence of the RC mechanism at high pressures in a medium-sized molecular system, analogous to earlier observations for larger systems such as the dimerization of benzyl radicals (Luther et al., Phys. Chem. Chem. Phys. 2004, 6, 4133)
Meniscium maxonianum R. S. Fernandes & Salino, comb. nov.
No full textMeniscium maxonianum (A.R.Sm.) R.S.Fernandes & Salino, comb. nov. Thelypteris maxoniana Smith (1992: 72). Type:— PERU. Maynas: Quistococha, vicinity of Iquitos, 18 Nov 1977, A. Gentry 20751 (holotype MO, isotype UC). Dryopteris desvauxii f. glandulosa Maxon & Morton (1938: 372) , Thelypteris longifolia f. glandulosa (Maxon & Morton 1938: 372) Morton (1967: 52) . Type:— BRASIL. São Paulo: Morro das Pedras, A.C. Brade 5753 (holotype NY). Selected specimens examined: — COLOMBIA. Comisaría Del Caquetá: Florencia, 400 m, 29 March 1940, J . Cuatrecasas 8855 (US).— VENEZUELA. Aragua: Tovar, A. Fendler 232 (K). Bolivar: Raul Leoni, 06°34’N, 66°23’W, 800 m, June 1989, A. Fernandez 5637 (MO).— PERU. Loreto: Mishuyacu, 100 m, April 1930, G . Klung 1255 (F, NY).— BRAZIL. Distrito Federal: Parque Municipal do Gama, 700–1000 m, 3 September 1964, H. S . Irwin & T. R. Soderstrom 5880 (F, K, NY); Goiás: A . Glaziou 22632 (F, P, US). Mato Grosso: Serra do Roncador, 550 m, H. S . Irwin et al. 16304 (F); Paraná: Paranaguá, Ilha do Mel, 25°30’44’’S, 48°19’08’’W, 3 m, 15 February 2004, P. H . Labiak et al. 3133 (UPCB). Pará: Parauapebas, 06°06’06’’S, 50°11’07’’W, 720 m, 20 April 2012, A. J . Arruda et al. 963 (BHCB). Santa Catarina: Brusque, 27°06’03’’S, 48°53’48’’W, 112 m, 05 June 2009, A. L . Gasper & E. Brogni 2173 (FURB).— BOLIVIA. 22 September 1901, R. S . Williams 1281 (NY, US). Distribution and habitat:— Meniscium maxonianum is distributed in Venezuela, Colombia, Peru to Bolivia and Brazil. It grows in forest formations of Amazonian forest, Atlantic rain forest, and Cerrado domains, where it can grow in shaded and sunny areas at 1– 720 m. Notes:— The most notable character of M. maxonianum is the dense cover of sessile to stalked glands on the abaxial surface of the laminae, and having the sporangial stalks glabrous or with inconspicuous filamentous, septate structures. In these characters it differs from the similar M. longifolium, which shares the same shape of lamina and pinnae, but is characterized by having glands and trichomes (sometimes only trichomes) on the abaxial surface of the lamina and sporangial stalks with long, acicular trichomes. Another species that also has glandular trichomes on the abaxial surface of the lamina is M. falcatum Liebmann (1849: 183). However, it differs from M. maxonianum by having longer pinna stalks and acicular and erect trichomes on the costae.Published as part of Fernandes, Rozijane Santos, Yesilyurt, Jovita Cislinski & Salino, Alexandre, 2014, New species and combinations in Meniscium (Thelypteridaceae), pp. 1-11 in Phytotaxa 184 (1) on page 9, DOI: 10.11646/phytotaxa.184.1.1, http://zenodo.org/record/515317
Meniscium cocleanum R. S. Fernandes & Salino 2014, comb. nov.
No full textMeniscium cocleanum (A.R.Sm. & Lellinger) R.S.Fernandes & Salino, comb. nov. Thelypteris cocleana Smith & Lellinger (1985: 918). Type:— PANAMA. Coclé: “El Copé, along gravel road to right before sawmill, 2400 ft,” Province of Coclé, 731 m, 18 October 1979, T. Antonio 2188 (holotype UC, isotype MO). Selected specimens examined:— NICARAGUA. Rio San Juan, Caltillo, Reserva Indio-Maiz, Cerro el Diablo, 11°01’N, 84°12’W, 350–609 m, 9 December 1998, R . Rueda et al. 9689 (MO). COSTA RICA. Guanacaste, Cantón de Tilaran, 10°37’40’’N, 84°59’45’’W, 1050 m, 26 July 1995, A . Rojas & Rodríguez 2089 (BM, MO); Canton de La Cruz, 10°59’25’’N, 85°25’40’’W, 700–800 m, 4 September 1996, A . Rojas & M. Mata 2996 (UC). PANAMA. Coclé. El Cope, Parque Nacional G.D. Omar Torrijos Herrera, 08°40’13’’N, 80°35’26’’W, 725 m, 7 July 2012, A . Salino et al. 15361 (BHCB); Veraguas, 08°35’N, 81°05’W, 1100–1400 m, 15 July 1983, C . Hamilton & K. Krager 3981 (UC), 20 February 1983, C . Hamilton & R. Dressler 3069 (MO, UC), 3 April 1980, T . Antonio 3958 (MO); Coclé, 19 January 1978, T. B . Croat 44555 (MO, UC). Distribution and habitat:— Meniscium cocleanum is distributed from Nicaragua, Costa Rica, and Panama. It usually grows inside or along the edges of tropical evergreen forest formations, on hillsides, often along trails, at 350–1050 m. Notes:— Meniscium cocleanum was, until this study, the only species of the genus known to have buds in the distal pinnae. Smith & Lellinger (1985) stated that the affinities of this species are uncertain. The new species described in this paper (Meniscium triangularis) also has distal proliferous buds, however, M. cocleanum has completely glabrous laminae whereas M. triangularis has a dense indument of scales and trichomes abaxially. Other differences have been previously discussed above.Published as part of Fernandes, Rozijane Santos, Yesilyurt, Jovita Cislinski & Salino, Alexandre, 2014, New species and combinations in Meniscium (Thelypteridaceae), pp. 1-11 in Phytotaxa 184 (1) on pages 7-8, DOI: 10.11646/phytotaxa.184.1.1, http://zenodo.org/record/515317
Emergence of Governance Structure in Collaborative University–Industry R&D Programs
No full textThis chapter explains how the governance structure of university–industry collaboration programs evolves while transitioning from the strategic planning phase to the execution and delivery phase. A transitional phase is introduced between the two official phases of the program life cycle, over which the Program and Project Management Office (PgPMO) emerges, providing tools to support the program governance. Along with this transition, the three main collaborators—university, industry, and government—change their roles to support achieving the goals of the collaboration. The four drivers for the emergence of governance structure are fairness, transparency, responsibility, and accountability, according to which the main actors in the governance of program change their roles switching between leadership, partnership, and serving other actors
Synopsis of the Darwin wasp Chirotica Förster, 1869 (Hymenoptera: Ichneumonidae: Phygadeuontinae) in Brazil
No full textLima, Adriane G. M., Fernandes, Daniell R. R. (2024): Synopsis of the Darwin wasp Chirotica Förster, 1869 (Hymenoptera: Ichneumonidae: Phygadeuontinae) in Brazil. Zootaxa 5418 (2): 101-139, DOI: 10.11646/zootaxa.5418.2.1, URL: http://dx.doi.org/10.11646/zootaxa.5418.2.
Tibraca exigua Fernandes & Grazia 1998
No full textTibraca exigua Fernandes & Grazia, 1998 (Figs 109–112) Tibraca exigua Fernandes & Grazia, 1998: 1057. Material studied. Camaquã: 1♂, 08.V.1991, H. Moreira leg. (UFRG). Pelotas: 1♀, VI.1991, Marcolin leg. (UFRG); 1♂, 10.VI.1990, M. N. Miranda leg. (UFRG); 1♂, 20.II.1991, P. Welzel leg. (UFRG); 1♂, V.1991, R. Zepra leg. (UFRG); 1♀, 28.IV.1991, R. Von Laer leg. (UFRG); 1♂, III.1991, Silveira leg. (UFRG); 1♂, 27.V.1994, J. T. Zanusso leg. (UFRG); VI.1990, 1♂, Costa leg. (UFRG); 27.IV.1993, 1♂, O. Maguelly leg. (MCNZ); 1♂, VI.1990, Marques leg. (UFRG); 1♂, V.1990, Schallens leg. (UFRG); 1♂, IV.1991, Monteiro leg. (UFRG); 1♂, 26.X.1994, I. M. Silva leg. (UFRG); 1♀, 17.III.1991, H. Gastal leg. (UFRG); 1♂, 17.V.1991, D. Chapon leg. (MECB). São Francisco de Paula: 1♀, 17–19.XII.2005, V. C. Matesco leg. (UFRG). Diagnostic features. Body dorsal and ventral surfaces dark castaneous (Fig. 109, 111). Head longer than wide. Mandibular plates shorter than clypeus, rounded apically (Fig. 110). Clypeus robust and raised above the mandibular plates. Antennomere 2 smaller than the first (Fig. 110, red arrow). Anterolateral margins of pronotum impunctate or rarely punctate at the lateral portion (Fig. 110). Internal angles of cicatrices of pronotum with pale yellow callosity. Humeral angles slightly developed (Fig. 110).Apex of radial vein of corium with pale yellow callosity. Connexivum castaneous with margin light castaneous and a small black spot at the apex (Fig. 109). Body length: 9.00–12.00 mm (Fernandes & Grazia 1998). Recorded host plants. Rice (Fernandes & Grazia 1998). Distribution in Rio Grande do Sul. Camaquã, Canguçu, Capão do Leão, Pelotas and São Francisco de Paula (Fig. 112). Comments. This species is similar to T. limbativentris, being differentiated by its darker color and smaller body size.Published as part of Barros, Lurdiana D., Paim, Marcelo R., Krein, Verônica, Carabajal, Victor, Brandão, Marcela N., Bernardes, Paula De O. & Lindner, Mariana F., 2021, Illustrated guide to Pentatominae (Hemiptera: Pentatomidae) species associated with the four main grain crops in Rio Grande do Sul state, Brazil, pp. 430-478 in Zootaxa 4958 (1) on pages 468-469, DOI: 10.11646/zootaxa.4958.1.27, http://zenodo.org/record/469217
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