34,292 research outputs found
Herbertia amabilis Deble & F. S. Alves 2013, spec. nova
<i>Herbertia amabilis</i> Deble & F. S. Alves, spec. nova (Fig. 1, 2). <p> <b>Typus: BRAZIL. Rio Grande do Sul:</b> Júlio de Castilhos, “no campo, entre gramíneas, no solo argiloso, flores brancas”, 29°18’43’’S 53°49’39’W, 23.XII.2010, fl. fr., <i>L. P.Deble 12721, A.S. de Oliveira-Deble, J. N. C. Marchiori & F. S. Alves</i> (holo-: SI!; iso-: CTES!, ICN!).</p> <p> <i>Species nova ab Herbertiae lahue subsp. amoenae affinis, sed magna statura (30-40 cm alta vs 8-15 cm alta), foliis longioribus et anguste linearis (18-35 cm longis, 0.3-0.5 cm latisvs 8-15 cm longis, 0.4-1 cm latis),ovarium obovatoclavatum, 3.5-5 mm longum (versus obovato-oblongum, 6-8 mm longum), tepala exteriora albida, (vs coeruleo-violacea</i>),tepalainteriora albida et lutea (vs atro-violacea), <i>optime distincta.</i></p> <p> <i>Plants</i> up to 30-40 cm high, subterranean stems 10-20 cm long. <i>Bulb</i> ovoid, 18-24 mm wide, sometimes prolonged in a short collar. <i>Leaves</i> 2, plicate, narrowly linear, 18-35 cm long, 0.3-0.5 cm wide. <i>Spathes</i> 2-4, herbaceous, pallid-green, bivalved, two-flowered, pedunculate, peduncles 4-8.5 cm long; lower valve 2.3-3.4 cm long, the upper 3.5-4.5 cm long, both with membranous edges; pedicel filiform, 4-5 cm long. <i>Flowers</i> predominately white, radially symmetrical, 3.5-4 cm diam. <i>Tepals</i> whorls sharply dissimilar: outer tepals obovate, 18-21 mm long, 9-12 mm wide, white, with yellow dots scattered in the proximal half, and a yellow medial stripe at the base; inner tepals oblanceolate, 5-6 mm long, 1.3-1.8 mm wide, white, with a yellow macula in medial portion, apex long attenuate, acuminate, reflexed. <i>Filaments</i> entirely united in a column, 4.2-4.8 mm long, yellowish along the column; anthers linear, yellow, curved at dehiscence, 7-7.5 mm long; pollen yellow. <i>Ovary</i> obovate-clavate, 3.5-5 mm long, 1.8-2.5 mm wide. <i>Style</i> 9-9.5 mm long; style arms channeled, 4.5-5 mm long, at the apex bifid for 1.8-2.2 mm, the divisions divaricate, recurved, apically stigmatic. <i>Capsules</i> broadly oblong-clavate, 9-11 mm long, 4.5-5 mm wide. <i>Seeds</i> oblong to obconical, angular, reddish-brown, epidermis striate, 1.5-2 mm long.</p> <p> <i>Etymology. –</i> The specific epithet means kind, delicate and refers to the pretty and delicate flowers of the new species.</p> <p> <i>Distribution and ecology. – Herbertia amabilis</i> is a narrow endemic of central Rio Grande do Sul State, where just two populations are known. Plants grow in grasslands on clay soils in the hydrographic basin of the Guassupi river southwest of Júlio de Castilhos city (Fig. 3).</p> <p> <i>Phenology. –</i> Flowering and fruiting occur during December.</p> <p> <i>Conservation. –</i> During the review of herbaria, no exsiccates of <i>H. amabilis</i> were found. The only known collections are those made by the authors and here cited. The extent of occurrence of <i>H. amabilis</i> comprises less than 100 km 2 and the populations size are smaller than 10 km 2; only two populations are know and with few individuals. Furthermore, agriculture, and urban expansion affect directly the range of the species. Due to the rarity, fragmentation of populations, and observed threats, it seems prudent to include <i>H. amabilis</i> in a preliminary status of Critically Endangered category of the IUCN Red List of Endangered plant species according to the following criteria “CR B1, 2a, b; D” (IUCN, 2011).</p> <p> <i>Taxonomical note. – Herbertia amabilis</i> by its androgynoecium filaments entirely united forming a column, its ascendant style arms, and the size of flowers is most closely related with <i>H. lahue</i> subsp. <i>amoena</i>, but can be segregated by the following features: robust habit (30-40 cm vs 8-15 cm), narrowly linear leaves, with 18-35 cm long, 0.3-0.5 cm wide (vs linear-lanceolate leaves, with 8-15 cm long, 0.4-1 cm wide), style arms at the apex recurved (vs not or slightly recurved), and ovary obovate-clavate, 3.5-5 mm long (vs obovate-oblong, 6-8 mm long). Additionally, the flowers are predominately white (vs blue-violet, rarely white in atypical individuals occurring among normal ones), with a yellow macula in medial portion of inner tepals (vs without yellow macula). <i>Herbertia crosae</i>, another close species differs by purple dots along the column of androgynoecium filaments (vs without purple dots), free apically up to 1 mm long (vs entirely united), and smaller anthers (4-5 mm vs 7-7.5 mm long). <i>Herbertia darwinii</i> has androgynoecium features similar with the new species, but its differs by large 4-5.7 cm wide, blue-violet flowers, ovary 6- 8.5 mm long, and leaves 1-2 cm wide.</p> <p> <i>Paratypus. –</i> <b>BRAZIL. Rio Grande do Sul:</b> Júlio de Castilhos, “no campo, entre gramíneas, no solo argiloso, flores brancas”, 29°18’43’’S 53°49’39’W, 23.XII.2010, fr, <i>L. P. Deble 12722, A. S. de Oliveira-Deble, J. N. C. Marchiori & F. S. Alves</i> (CTES!).</p>Published as part of <i>Deble, Leonardo Paz & Alves, Fabiano da Silva, 2013, Herbertia amabilis Deble & F. S. Alves (Iridaceae), a new species from Brazil, pp. 133-137 in Candollea 68 (1)</i> on pages 134-136, DOI: 10.15553/c2013v681a18, <a href="http://zenodo.org/record/5715240">http://zenodo.org/record/5715240</a>
A sinfonia do sagrado em Castro Alves: (Deus, Eros e mãe em Os escravos)
Tese (doutorado) - Universidade Federal de Santa Catarina, Centro de Comunicação e Expressão. Programa de Pós-Graduação em Literatura.No presente trabalho realiza-se uma leitura intertextual entre a Bíblia e Os escravos, coletânea de poemas de teor abolicionista do poeta romântico Antônio Frederico de Castro Alves (1847-1871), objetivando demonstrar que os textos poéticos arquitetam-se na desconstrução e reconstrução dos textos bíblicos. A leitura dos poemas centra-se nos personagens: Deus, Eros e Mãe, os quais conformam uma trindade poética/sagrada. A pesquisa divide-se em três movimentos: Prelúdios do sagrado no Romantismo, Tríade melódica e À guisa de coda: trindade poética. No primeiro efetuam-se algumas aproximações ao conceito do sagrado e aos Romantismos francês e brasileiro. O seguinte corresponde à leitura das composições, através das linhas melódicas: A dualidade de Deus, A ambivalência de Eros e O duplo calvário da Mãe escrava. E no último movimento amalgamam-se as inter-relações entre a trindade cristã e poética e os dramas bíblico e poético
Pilumnoides coelhoi Guinot & Macpherson 1987
Pilumnoides coelhoi Guinot & Macpherson, 1987 (Figure 6D) Material examined. Penaeid—18 (1 M, 11 F, 5 OF, 1 J); size range: 1.05 ≤ CW ≤ 8.40 mm; average: CW = 5.67 ± 2.10 mm; CZUFS CRU- 00255. Stations. Penaeid—3, 5, and 9. Distribution. Western Atlantic—Brazil (from Sergipe to Santa Catarina, and Abrolhos) (Melo 1996; Serejo et al. 2006; Barros-Alves et al. 2015). Ecological notes. From shallow waters to 30 m. On sand bottoms or among algae (Melo 2008). Previous records in Sergipe. Barros-Alves et al. (2015).Published as part of Mendonça, Luana M. C., Guimarães, Carmen R. P., Santos, Rafael C., Alves, Douglas F. R., Barros-Alves, Samara P., Silva, Sonja L. R. & Hirose, Gustavo L., 2019, Decapod crustaceans from the continental shelf of Sergipe, northeastern Brazil, pp. 301-344 in Zootaxa 4712 (3) on page 325, DOI: 10.11646/zootaxa.4712.3.1, http://zenodo.org/record/358631
Merremia macrocalyx O'Donell 1941
27. Merremia macrocalyx (Ruiz & Pav.) O’Donell Venezuela, Ecuador, Bolivia, Brazil (widely distributed). Selected Vouchers:—Zambana, Albuquerque 525 (IPA, ULM); Piedade, Alves-Araújo & Araújo 723 (UFP). 28. Merremia umbellata (L.) Hallier f. United States, Mexico, Central America, Caribbean, Venezuela, Colombia, Ecuador, Bolivia, Brazil (Amapá, Rondônia, Amazonas, Pará, Ceará, Pernambuco), Argentina. Selected Voucher:—Zambana, Alves-Araújo et al. 665 (UFP); Piedade, Alves-Araújo 561 (UFP). 28. Merremia umbellata (L.) Hallier f. United States, Mexico, Central America, Caribbean, Venezuela, Colombia, Ecuador, Bolivia, Brazil (Amapá, Rondônia, Amazonas, Pará, Ceará, Pernambuco), Argentina. Selected Voucher:—Zambana, Alves-Araújo et al. 665 (UFP); Piedade, Alves-Araújo 561 (UFP).Published as part of Araújo, Diogo & Alves, Marccus, 2010, Climbing plants of a fragmented area of lowland Atlantic Forest, Igarassu, Pernambuco (northeastern Brazil), pp. 1-24 in Phytotaxa 8 on page 17, DOI: 10.11646/phytotaxa.8.1.1, http://zenodo.org/record/489386
Paractaea nodosa
Paractaea nodosa (Stimpson, 1860) Material examined. Petro-UFS—1 F; CW = 12.10 mm; CZUFS CRU- 00108. Station. Petro-UFS—8. Distribution. Western Atlantic—North Carolina, Florida, Gulf of Mexico, Antilles, the north of South America, Brazil (from Amapá to São Paulo), and Uruguay (Melo 1996; Alves et al. 2012). Ecological notes. On coral reefs and sand, gravel, rock, and mud bottoms (Melo 1996). Previous records in Sergipe. Barreto et al. (1993).Published as part of Mendonça, Luana M. C., Guimarães, Carmen R. P., Santos, Rafael C., Alves, Douglas F. R., Barros-Alves, Samara P., Silva, Sonja L. R. & Hirose, Gustavo L., 2019, Decapod crustaceans from the continental shelf of Sergipe, northeastern Brazil, pp. 301-344 in Zootaxa 4712 (3) on page 326, DOI: 10.11646/zootaxa.4712.3.1, http://zenodo.org/record/358631
Garthiope spinipes
Garthiope spinipes (A. Milne-Edwards, 1880) Material examined. Penaeid—2 F; size range: 5.93 ≤ CW ≤ 7.36 mm; average: CW = 5.65 ± 1.01 mm; CZUFS CRU- 00254. Station. Penaeid—3. Distribution. Western Atlantic—USA (Bermuda, Florida, and Gulf of Mexico), Venezuela, and Brazil (from Amapá to Espírito Santo, and São Paulo) (Melo 1996; Alves et al. 2006). Ecological notes. From intertidal to 60 m. Under coral reefs, sponges, and on sand (Melo 1996). Previous records in Sergipe. None.Published as part of Mendonça, Luana M. C., Guimarães, Carmen R. P., Santos, Rafael C., Alves, Douglas F. R., Barros-Alves, Samara P., Silva, Sonja L. R. & Hirose, Gustavo L., 2019, Decapod crustaceans from the continental shelf of Sergipe, northeastern Brazil, pp. 301-344 in Zootaxa 4712 (3) on page 326, DOI: 10.11646/zootaxa.4712.3.1, http://zenodo.org/record/358631
Merremia umbellata
28. Merremia umbellata (L.) Hallier f. United States, Mexico, Central America, Caribbean, Venezuela, Colombia, Ecuador, Bolivia, Brazil (Amapá, Rondônia, Amazonas, Pará, Ceará, Pernambuco), Argentina. Selected Voucher:—Zambana, Alves-Araújo et al. 665 (UFP); Piedade, Alves-Araújo 561 (UFP).Published as part of Araújo, Diogo & Alves, Marccus, 2010, Climbing plants of a fragmented area of lowland Atlantic Forest, Igarassu, Pernambuco (northeastern Brazil), pp. 1-24 in Phytotaxa 8 on page 17, DOI: 10.11646/phytotaxa.8.1.1, http://zenodo.org/record/489386
Reactive Orange 16 dye degradation in anaerobic and aerobic MBBR coupled with ozonation: addressing pathways and performance
In this study, two treatment routes were investigated for degradation of the azo dye Reactive Orange 16 (RO16): biodegradation in an anaerobic MBBR (R1) and ozonation followed by biological treatment in an aerobic MBBR (R2). Along with the dye, glucose and nutrients were supplemented to the influent fed to R1 as carbon co-substrate and nitrogen source, respectively. In R1, maximum color removal of 61 ± 18% was achieved for 5 mg l−1 of dye, hydraulic retention time of 12 h and influent COD of 800 mg l−1. Moreover, RO16 biodegradation was limited by carbon source (glucose) and attached solids concentrations. Batch tests revealed that anaerobic biodegradation of the dye and glucose followed second-order kinetics and RO16 degradation constant increased as the initial COD was reduced. Considering the relatively low color removal achieved anaerobically, dye solutions (100 to 500 mg l−1) were ozonated, enabling fast discoloration of at least 97% within 20 min for the highest dye concentration. However, the low COD (50–75%) and TOC (35–40%) removals achieved indicate that only partial mineralization occurred. RO16 (500 mg l−1) ozonation products were identified, and a degradation pathway was proposed. Subsequently, the ozonated solutions were supplemented with glucose and nutrients and fed to R2. COD removal decreased considerably (from 92 to 81%) when ozonated solutions with original dye concentration of 500 mg l−1 were fed to R2, but ammonium removal remained fairly stable. Three compounds identified before biological treatment were not found in R2 effluent, suggesting that they were biodegraded
Lysmata bahia Rhyne & Lin 2006
Lysmata bahia Rhyne & Lin, 2006 (Figure 7F) Material examined. Penaeid—1 OF; CL: 9.4 mm; CZUFS CRU- 00317. Stations. Penaeid—4. Distribution. Western Atlantic—Panama (Bocas Del Toro), and Brazil (Ceará, Sergipe, Bahia, Rio de Janeiro, and São Paulo) (Rhyne & Lin 2006; Baeza 2008; Barros-Alves et al. 2015; Pachelle et al. 2016). Ecological notes. Found at 5 m depth, on non-consolidated bottoms, on reefs, and inside calcareous algae (Almeida et al. 2012). Remarks. Part of a monophyletic group composed of Lysmata gacilirostris Wicksten, L. pederseni Rhyne & Lin, L. ankeri Rhyne & Lin, L. nayaritensis Wiksten, L. californica (Stimpson), and L. bahia supported by phylogenetic analysis (Baeza 2010). Previous records in Sergipe. Barros-Alves et al. (2015).Published as part of Mendonça, Luana M. C., Guimarães, Carmen R. P., Santos, Rafael C., Alves, Douglas F. R., Barros-Alves, Samara P., Silva, Sonja L. R. & Hirose, Gustavo L., 2019, Decapod crustaceans from the continental shelf of Sergipe, northeastern Brazil, pp. 301-344 in Zootaxa 4712 (3) on page 330, DOI: 10.11646/zootaxa.4712.3.1, http://zenodo.org/record/358631
Triethylene glycol recovery by an energetically intensified thermosyphon-assisted falling film distillation unit: Experimental assessment on a pilot-scale unit and in-silico comparison with a conventional column from natural gas processing
Facing the emerging needs for energy-enhanced separation units, this work evaluated the triethylene glycol (TEG) regeneration, used as a dehydrating agent of natural gas from wells, by a novel thermosyphon-assisted falling film distillation technology, called Destubcal. The pilot-scale device has an innovative heat supply through a two-phase closed thermosyphon, which ensures a uniform energy distribution along the entire distillation tube. Based on current operating data from industrial water-rich TEG streams, different operating conditions were performed in the pilot-scale unit. The best recovery ratio (99.0%) was obtained with an evaporator temperature of 180 °C and a feed flow rate of 15 L/h. However, in order to maximize the bottom TEG composition, the best experimental condition achieved was 17 L/h and bottom temperature of 152.07 °C, due to an evaporator temperature of 170 °C. As a result, the Destubcal unit saved around 38.4% in energy requirement and reduced 49% the column height when compared to a conventional distillation column for the same recovery degree. Therefore, the proposed Destubcal technology can be considered a feasible alternative as recovery column for TEG regeneration in natural gas beneficiation units, with advantages of reduced dimensions and energy-saving operation
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