631 research outputs found

    Dysschema wayneri Moraes, sp.nov.

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    Dysschema wayneri Moraes sp.nov. (Figs. 3–4, 16– 22) Diagnosis (♂). Tegulae with a yellow macula, near the outter margin and medio-distal portion of the outter margin with white scales. Discal region of hindwing with veins lined with brown scales, more evident on the trunk of CuA. Aedeagus with lobe of vesica near to the ejaculatory duct with micro spicules. Description (♂). Head. Frons light brown, vertex with white scales. Labial palp brown. Thorax. Predominantly light brown. Prothoracic collar with two white maculae; prothoracic coxa white. Tegulae with a yellow basal macula, near the outer margin; medial-distal portion of the outer margin with white scales. Forewing light brown, three region with yellowish semihyaline maculae: (i) triangular on the basal region, between the trunk of R vein and 1 A+ 2 A, (ii) rounded, on the median region, between the trunk of R vein and the tornus, (iii) on the subapical region, oblique, between R 4 and CuA 1; brown band, faded, since the trunk of R vein, on the middle of discal cell, reaching the inner margin; brown macula on the region of closure of discal cell; white maculae on the wing base, on the trunk of R vein; ventral surface with the same dorsal pattern and with a yellow macula on the basal region of costal margin. Hindwing with the costal and outer margins brown, discal region semihyaline and veins lined with brown scales, more evident on the trunk of CuA; region of closure of discal cell lined with brown scales; ventral surface with the same dorsal pattern, but with a yellow macula on the base of costal margin. Abdomen. Dorsally brown with two yellow bands from A 2 to A 7; ventrally yellow with a central brown stripe. Tuffs of yellow scales at the terminal portion of the abdomen. Genitalia (Figs. 16–22). Tegumen trapezoidal in dorsal view, with the anterior margin straight, and acute posterolateral projections. Uncus bifid, not fused to the tegumen; arms of uncus fused in the anterior portion, not ventrally projected. Valva elliptical; costa with medial apodeme (lacinia), distal apodeme oblique, extended by the inner surface of valva to its middle portion; sacculus developed, consisting of a fold on the inner surface of the valva, oriented towards distal-medial axis; harpe subtriangular; cucullus digitiform; valvula spatulate. Transtilla sclerotized not articulated with the valva and not fused to the juxta. Juxta sclerotized, as an inverted “U”. Saccus without anterior projections. Subscaphium smooth. Aedeagus rectilinear and smooth; ejaculatory bulb rounded, foramen lateral; vesica bilobated, apex of the lobe opposite to the opening of ejaculatory duct sclerotized, lobe near to the ejaculatory duct with microspicules, everted portion of the ejaculatory duct smooth. Female. Unknown. Etymology. The specific epithet is granted in honor to Wayner Souza Tapajós Lyra, friend who helped senior author during his Ph.D. project, when the species was discovered. Distribution. The records suggest an endemic distribution in montane mixed ompbrophylous forest of medium and high altitudes in the States of São Paulo and Rio de Janeiro. Remarks. Although this species is morphologically distinct for the wing pattern, the morphology of the genitalia of D. wayneri resembles that of D. neda (Klug, 1836), differing by not having the uncus fused to the tegumen and by the distinct morphology of the cucullus and the valvula. Type-serie. HOLOTYPE ♂: BRAZIL: São Paulo, Campos do Jordão, Turiba, 1800m, 13 / 15 -ii- 1953, Travasso Filho & Travassos col. (MZSP). PARATYPES: BRAZIL: São Paulo, Campos do Jordão, Turiba, 1800m, 13 / 15 -ii- 1953, Travassos Filho & Travassos col., 1 ♂ (BMNH), 1 ♂ (MZSP), 1 ♂ (USNM); Campos do Jordão, Itapeva, 1700m, 15 -i- 1953, L.Trav Filho & S. Medeiros col., 1 ♂ (MZSP); Campos do Jordão, Lagoinha, 1500m, 14 -ii- 1953, Travasso Filho & Travassos col., 1 ♂ (MZSP). Rio de Janeiro, Itatiaia, Estrada do Rio Brasil, 1300m, 5 / 8 - 3-1951, Trav & D. Albuquerque col., 1 ♂ (MZSP). Material examined. BRAZIL: Minas Gerais: Itamonte, Vargem Grande, 1 ♂ (DZUP). Rio de Janeiro: Itatiaia, Estrada Agulhas Negras KM 6, 1 ♂ (DZUP); Itatiaia, Estrada do Rio Brasil, 4 ♂♂ (DZUP), 1 ♂ (MZSP); Itatiaia, Macieira, 1 ♂ (DZUP). São Paulo: Campos do Jordão, Itapeva, 4 ♂♂ (MZSP); Campos do Jordão, Lagoinha, 3 ♂♂ (MZSP); Campos do Jordão, Turiba, 24 ♂♂ (MZSP); Campos do Jordão, Umuarama, 3 ♂♂ (DZUP). Without labels, 1 ♂ (MZSP).Published as part of Moraes, Simeão De Souza & Duarte, Marcelo, 2015, Description of four new species of the tiger moth genus Dysschema Hübner (Lepidoptera: Erebidae, Arctiinae, Arctiini, Pericopina), pp. 540-550 in Zootaxa 4006 (3) on pages 544-546, DOI: 10.11646/zootaxa.4006.3.7, http://zenodo.org/record/23868

    Dysschema uriasi Moraes, sp.nov.

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    Dysschema uriasi Moraes sp.nov. (Figs. 1–2, 9– 15) Diagnosis (♂). Tegulae with a reddish basal macula near the outer margin. Ventral surface of forewing and hindwing with a red macula on the base of costal margin, discal region of hingwing semihyaline yellowish. Valva with subtriangular harpe and vavula absent. Description (♂). Head. Frons, vertex and labial palp brown. Thorax. Predominantly brown. Prothoracic collar with two yellow maculae; prothoracic coxa brown. Tegulae with a reddish basal macula, near the outer margin. Forewing brown, three region with whitish semihyaline maculae: (i) on the basal region, between the trunk of R vein and the inner margin, (ii) on the median region, between the trunk of R vein and the inner margin, with the distal margin of the maculae with rounded contour, touching the subapical macula between M 3 and CuA 1, (iii) on the subapical region, oblique, between the costal margin and e CuA 1; dark-brown band, since the trunk of R vein, on the middle of discal cell, reaching the inner margin, faded between the trunk of CuA e CuP; dark brown macula on the region of closure of discal cell; two maculae on the wing base, reddish on the trunk of R vein and white on the trunk of CuA; ventral surface with the same dorsal pattern. Hindwing with the costal and outer margins brown, discal region yellowish semi hialyne, region of closure of discal cell lined with brown scales; ventral surface with the same dorsal pattern, but with a red macula on the base of costal margin. Abdomen. Dorsally brown with two light brown faded bands on A 2 reaching A 8; ventrally light brown with two lateral bands formed by yellow maculae on the segments A 2 -A 8. Tuffs of reddish scales at the terminal portion of the abdomen. Genitalia (Figs. 9–15). Tegumen trapezoidal in dorsal view straight anteriorly, with acute posterolateral projections. Uncus bifid, not fused to the tegumen; arms of uncus fused in the anterior portion, not ventrally projected. Valva subelliptical; costa with medial apodeme (lacinia) acute, distal apodeme oblique, extended by the inner surface of valva to its middle portion; sacculus developed, consisting of a fold on the inner surface of the valva, oriented towards distal-medial axis; harpe subtriangular; cucullus digitiform; valvula indistinct. Transtilla sclerotized not articulated with the valva and not fused to the juxta. Juxta sclerotized, shaped like an inverted “U”. Saccus without anterior projections. Subscaphium smooth. Aedeagus straight and smooth; ejaculatory bulb rounded, foramen lateral; vesica bilobated, apex of the lobe opposite to the opening of ejaculatory duct sclerotized, lobe near to the ejaculatory duct smooth, everted portion of the ejaculatory duct smooth. Female: Unknown Etymology. The specific epithet is granted in honor to Rodrigo Urias dos Santos, partner of the senior author to whom he dedicates his love. Distribution. The few records for this species suggest an endemic distribution to montane dense ombrophilous forest of medium and high altitudes in the States of São Paulo and Rio de Janeiro. Remarks: This species is known only by males. The wing pattern is similar to D. hilara (Weymer, 1895). However, D. uriasi is distinguished by having whitish color marks on the hindwings, and a red prothoracic collar Type series. HOLOTYPE ♂: BRAZIL: São Paulo: Campos do Jordão, Faz[enda]. Guarda Pinheiro Seco, 1750m, 18 -iii- 1954, Rabelo, P. Biase & L. Trav. F. col., (MZSP). PARATYPES: BRAZIL: São Paulo: Campos do Jordão, Turiba, 13 -iii- 1953, Trav. Filho & Rabelo col., 1 ♂ (MZSP); Campos do Jordão, Faz[enda]. Guarda Pinheiro Seco, 1750m, 18 -iii- 1954, Rabelo, P. Biase e L. Trav. F. col., 1 ♂ (MZSP), 1 ♂ (USNM). Rio de Janeiro: Itatiaia, Estrada Agulhas Negras, 2000m, 10 / 11 -i- 1953, Pearson col., 1 ♂ (BMNH), 1 ♂ (MZSP ). Material examined. BRAZIL. Rio de Janeiro: Itatiaia, Estrada Agulhas Negras KM 5, 1 ♂ (BMNH), 2 ♂♂ (DZUP); Itatiaia, Macieira, 4 ♂♂ (DZUP). São Paulo: Campos do Jordão, Faz[enda]. Guarda Pinheiro Seco, 3 ♂♂ (MZSP); Campos do Jordão, Turiba, 1 ♂ (MZSP), Campos do Jordão, Umuarama, 2 ♂♂ (DZUP).Published as part of Moraes, Simeão De Souza & Duarte, Marcelo, 2015, Description of four new species of the tiger moth genus Dysschema Hübner (Lepidoptera: Erebidae, Arctiinae, Arctiini, Pericopina), pp. 540-550 in Zootaxa 4006 (3) on pages 541-544, DOI: 10.11646/zootaxa.4006.3.7, http://zenodo.org/record/23868

    Tenuipalpus isabelae Mesa, Moraes & Ochoa, 2006, n. sp.

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    <i>Tenuipalpus isabelae</i> n. sp. <p>(Figure 1 A–D)</p> <p> <b>Diagnosis</b>: This species belongs to the <i>keiensis</i> subgroup of the <i>proteae</i> group, established by Meyer (1993), whose adult females are characterized by having 6 pairs of dorsolateral opisthosomal setae, one pair of <i>Ic3</i> and 2 pairs of <i>Ic4</i>. Females of this new species resemble <i>T. barticanus</i> De Leon (1965), but differ by having 2 setae each on genua I and trochanter III (one seta each in <i>T. barticanus</i>), and prodorsal seta <i>sc2</i> about 4 times longer than in <i>T. barticanus</i>.</p> <p> Pará Veiga & Flechtmann (1980) <b>Adult female:</b> (Specimens measured: 5).</p> <p>Subcapitulum (rostrum) extending to base of femur I. Palpus (Fig. 1 C) with three segments; proximal segment without setae, intermediate segment with a dorsodistal pectinate seta; distal segment with one eupathidium 8 (7–9).</p> <p> Idiosoma (Fig. 1 A) 273 (260–282) long, 196 (187–200) wide. Rostral shield deeply cleft, with pointed lobes. Propodosoma with anterior margin irregular; dorsocentral region delimitated by two longitudinal grooves, with transversal striation; lateral regions with diagonal striation. Setae <i>v2</i> 7, <i>sc1</i> 8, smooth; <i>sc2</i> 43 (40–50), thick and serrate. Propodosomal pores absent.</p> <p> Dorsal surface of hysterosoma with 2 curved, roughly longitudinal grooves; region between grooves, anterior to opisthosomal pores, with transverse striation; remaining surface primarily smooth. Setae <i>c1</i> 5 (4–8), <i>c3</i> 16(14–20), <i>d3</i> 8 (6–9), <i>f2</i> 27 (25–30), <i>f3</i> 25 (23–28), <i>h1</i> 19 (18–22), all serrate; <i>h2</i> 100 (90–110) flagelliform, serrate proximally. Setae <i>d1</i>, <i>e1</i>, <i>e3</i> absent. Ventral surface (Fig. 1 D) with fine longitudinal striae between <i>Ic1</i> and <i>Ic2</i> and between <i>Ic3</i> and <i>Ic4</i>. Genitoventral plate lightly sclerotized, with fine transversal striae. Setae <i>Ic3a</i> 8 (7–9), <i>Ic4a</i> 62 (50–80) and <i>Ic4b</i> 55 (50–60), <i>ag</i> 19 (15–23); <i>g1</i> and <i>g2</i> 18 (15–23), on a transversal line.</p> <p>Chaetotaxy of legs I to IV: coxa 2/2/1/1, trochanter 1/1/2/1, femur 4/4/2/1, genu 2/2/0/ 0, tibia 5/5/3/3; tarsi I and II each with a serrate seta overlying distal solenidium.</p> <p> <b>Adult male</b>: unknown.</p> <p> <b>Deutonymph</b>: Idiosoma (Fig. B) 210 long, 185 wide. Setae <i>v2</i> 5, <i>sc1</i> 7, <i>c1</i> 2, <i>d3</i> 6 smooth, <i>sc2</i> 40, <i>c3</i> 22, <i>f2</i> 33, <i>f3</i> 27, <i>h1</i> 19, all serrate; <i>h2</i> 50, flagelliform, serrate proximally. Dorsal seta <i>e3</i> absent.</p> <p> <b>Type material</b>: Holotype female, 3 paratype females and 1 paratype deutonymph, ex <i>Actinostemon</i> sp. (Euphorbiaceae), VIII­2002, N.C. Mesa, Reserva Ecológica de Ibicatu, Piracicaba–SP, Brazil (22o46’43”S and 47o49’32”W). Deposited in the reference collection of Departamento de Entomologia, Fitopatologia e Zoologia Agrícola, Setor Zoologia, Escola Superior de Agricultura Luiz de Queiroz, Universidade de São Paulo, Piracicaba–SP, Brazil. One paratype female, same collection data, deposited in the National Museum of Natural History, Smithsonian Institution, Washington, DC, USA.</p> <p> <b>Etymology</b>: This species is named in honor Isabel Cristina Zuluaga Mesa, daughter of the senior author.</p>Published as part of <i>Mesa, N. C., De Moraes, G. J. & Ochoa, R., 2006, Two new species of Tenuipalpus (Acari: Tenuipalpidae) from southeastern Brazil, pp. 45-51 in Zootaxa 1138</i> on pages 45-48, DOI: <a href="http://zenodo.org/record/172028">10.5281/zenodo.172028</a&gt

    Transeius soniae Zannou, Moraes & Oliveira, n. sp.

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    Transeius soniae Zannou, Moraes & Oliveira, n. sp. (Fig. 23) DIAGNOSIS—Dorsal shield mostly smooth; ratios s 4:Z 1 = 8.2, s 4:S 2 = 1.4; seta j 3 ca. twice as long as j 1; seta z 4 about as long as distance between its base and that of s 4. Ventrianal shield smooth, subpentagonal. Spermatheca with calyx swollen basally, bladder-like, then narrowing and flaring distally. Male ventrianal shield with 6 pairs of preanal setae. FEMALE—(Specimens measured—Kenya: 7). Dorsum (Fig. 23 A)—Dorsal shield mostly smooth, striated anterolaterally and in region between Z 1 and Z 4, 346 (336–358) long and 202 (194–208) wide. Setae j 1 29 (27–30), j 3 55 (51–59), j 4 14 (13–16), j 5 12 (10– 13), j 6 10 (8–13), J 2 9 (8–10), J 5 9 (8–10), z 2 28 (26–30), z 4 33 (30–37), z 5 9 (8–10), Z 1 11 (11–13), Z 4 85 (82– 90), Z 5 99 (96–104), s 4 90 (82–104), S 2 63 (59–66), S 4 12 (11–13), S 5 10 (8–13), r 3 34 (32–37), R 1 19 (19–21). Setae smooth, except Z 4 and Z 5, lightly serrate. Peritreme—Extending forward to level of j 1. Venter (Fig. 23 B)—Sternal shield mostly smooth, with few lateral striae; posterior margin indistinct; distances between, St 1 -St 3 67 (64–70), St 2 -St 2 71 (70–74). Genital shield smooth; distance between St 5 -St 5 71 (67–77). Ventrianal shield smooth, subpentagonal, with slight constriction at level of preanal pores, anterior margin slightly convex, 129 (120–138) long, 89 (83–96) wide at level of Zv 2 and 83 (80–88) wide at level of anus; preanal pores elliptical and posteromesad to Jv 2. Chelicera (Fig. 23 C)—Movable digit 34 (34–35) long, with 3 teeth; fixed digit 30 long, with 10 teeth and a pilus dentilis. Spermatheca (Fig. 23 D)—Calyx of spermatheca swollen basally, bladder-like, then narrowing and flaring distally, 19 (16–21) long; atrium nodular. Legs—Macrosetae: Sge I 26 (22–29), Sge II 28 (24–32), Sge III 24 (22–26), Sti III 23 (21–24), Sge IV 51 (50–54), Sti IV 38 (35–42), St IV 69 (66–70). Chaetotaxy: genu II: 2 - 2 /1,2/ 1 - 1; genu III: 1-2 /1,2/ 0-1. MALE—(Specimen measured—Kenya: 1). Dorsum—Dorsal shield pattern as in female, 295 long and 183 wide. Setae j 1 25, j 3 48, j 4 13, j 5 10, j 6 10, J 2 8, J 5 8, z 2 23, z 4 33, z 5 8, Z 1 15, Z 4 68, Z 5 73, s 4 68, S 2 45, S 4 10, S 5 11, r 3 28, R 1 15. Setae smooth, except Z 4 and Z 5, lightly serrate. Peritreme—Extending forward to level between j 1 and j 3. Venter (Fig. 23 G)—Ventrianal shield subtriangular and reticulate, 135 long, 175 wide at the anterior corners, with 6 pairs of preanal setae, 1 pair of lateral lyrifissures posterior to Zv 2; preanal pores elliptical and posteromesad to Jv 2. Spermatodactyl (Fig. 23 F)—Without heel or toe, sinuous; shaft 23 long. Legs—Macrosetae: Sge I 20, Sge II 20, Sge III 18, Sge IV 40, Sti IV 30 and St IV 55. Chaetotaxy of genua II and III same as in female. LOCALITY AND TYPE MATERIAL—Holotype female, 8 paratype females and 1 allotype male from unknown plant, Machakos, Katumani, Kenya, 30 -IX- 1990, C., Kariuki, deposited at ESALQ-USP. ETYMOLOGY—This species is named in honor of Sonia Albigesi de Moraes, spouse of the second author of this paper. REMARKS—This species fits the characteristics given by Chant & McMurtry (2004) for their proximus species subgroup of the ablusus species group. Transeius avetianae (Arutunjan & Ohandjanian, 1972) differs from this species by having dorsal shield totally smooth, j 3 ca. 1.5 as long as j 1; s 4 and S 2 subequal in length. Transeius infundibulatus (Athias-Henriot, 1961) and Transeius proximus (Kolodochka, 1991) differ from the new species here described by having dorsal shield totally smooth and ventrianal shield pentagonal with transverse striae.Published as part of Zannou, Ignace D., De, Gilberto J., Ueckermann, Eddie A., Oliveira, Anibal R., Yaninek, John S. & Hanna, Rachid, 2007, Phytoseiid mites of the subtribe Amblyseiina (Acari: Phytoseiidae: Amblyseiini) from sub-Saharan Africa, pp. 1-47 in Zootaxa 1550 on pages 38-39, DOI: 10.5281/zenodo.17808

    Study about the genetic polymorphism of the αS1 - casein and ĸ - casein in goats from the Brazilian Northeast Semi Arid

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    A caprinocultura pela expressão sócio-econômica que representa para a população da região Nordeste, tem a necessidade da implantação de biotecnologias com a finalidade de melhorar a produtividade dos seus rebanhos. O estudo do polimorfismo genético do leite de animais criados nas condições zoosanitária e de bioclimatologia dessa região permitirá uma melhor correlação com as raças de produção e o conhecimento da composição do leite de cabras de diferentes raças. Objetivando realizar a genotipagem de cabras da raça Moxotó e Sem Raça Definida (SRD) provenientes do Semi Árido do Nordeste brasileiro(Pernambuco, Paraíba, Ceará e Rio Grande do Norte), por meio da técnica de PCR-RFLP (Polymerase Chain Reaction-Restriction Fragment Lenght Polymorfism), estudou-se o polimorfismo dos genes da αS1-caseína e ĸ-caseína. Foram colhidas amostras de sangue total, de caprinos adultos da raça Moxotóe SRD, do sexo feminino, sadios, criados de maneira extensiva; a extração do DNA leucocitário foi realizada por meio do protocolo de clorofórmio e fenol e os genes foram amplificados pela técnica de PCR com primers específicos para cada caseína. Em seguida foram utilizadas as enzimas XmnI (αS1-caseína) e HaeIII (ĸ-caseína) para obter o padrão de fragmentos das raças estudadas. Para a αS1-caseína obteve-se dois padrões de bandas representando os alelos B e D, sendo que a maioria dos animais apresentou o genótipo BB, enquanto o D apareceu em menor número associado ao B (B/D). Entre os animais da raça Moxotó, a frequência alélica observada foi de 96,03% para o genótipo BB e 3,97% para o genótipo B/D. Em relação aos animais SRD, a freqüência observada foi de 88,77% e 11, 23% para os genótipos BB e B/D, respectivamente. Não foi observada diferença estatística entre as raças nem entre os Estados estudados. No caso da ĸ-caseína, apenas o alelo A foi encontrado, caracterizando o monomorfismo para todos os animais estudados. Os resultados do presente estudo demonstraram a proximidade genética entre a raça Moxotó e os animais SRD, e dos rebanhos existentes nos estados do Nordeste incluídos nesta pesquisa, caracterizando a origem similar destes animais. Diante da detecção da maior presença do alelo B (forte) do gene da αS1-caseína nos animais estudados, admite-se a possibilidade de que fenotipicamente esses animais venham a exibir a característica de uma forte produção de proteínas, característica importante para o leite destinado à produção de queijos, favorecendo a caprinocultura da região.The goat raising, by the socio-economic expression that it represents for the population of the Northeast region, has the necessity of biotechnology implantation in order to improve the productivity of its herd. The study of genetic polymorphism of the milk of the animals raised in zoosanitary bioclimatology conditions of this region will permit a better correlation with the breed for reproduction and the knowledge of the milk composition of goats of different breeds. Aiming at the genotyping of Moxotó goats breed and mixed-breed goats from the Semi-Arid of Brazilian Northeast (Pernambuco, Paraíba, Ceará and Rio Grande do Norte), by means of PCR-RFLP technique (Polymerase Chain Reaction-Restriction Fragment Lenght Polymorfism), it was studied the polymorphism of the αS1-casein and ĸ-casein genes. It was collected total blood samples from adult Moxotó and mixed-breed goats, female, healthy, raised extensively; the leucocytary DNA extraction was made through chloroform and phenol protocol and the genes were ampReaction) with specific primers for each casein. After that, it was used XmnI enzymes(αS1-casein) and HaeIII (ĸ-casein) to obtain the pattern of fragments representing the B and D allele, being the majority of the animals presenting the BB genotype, while the D one appeared in a smaller number, associated to B (B/D). Among the animals of Moxotó breed, the allelic frequency observed was 96,03% for the genotype BB and 3,97% for the genotype B/D. In relation to the mixed-breed animals, the frequency was 88,77% and 11,23% for the genotypes BB and B/D, respectively. It was not observed statistic difference between the breeds nor the studied States. In the case of ĸ-casein, only the allele A was found, characterizing the monomorphism for all the animals studied. Based in the results of the present study, it is demonstrated a genetic proximity between Moxotó and mixed-breed of the exiting herd in the states of the Northeast included in this research, characterizing a similar origin of these animals. Before the detection of a higher presence of the allele B (strong) of the αS1-casein gene in thelified using the PCR technique (Polymerase Chainanimals studied, it is acknowledged the possibility that phenotypically these animals come to show the characteristic of a strong protein production, an important one for the milk destined to cheese production, favoring the goat raising in the region

    A Multiscale Method For Data Assimilation

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    In data assimilation problems, various types of data are naturally linked to different spatial resolutions (e.g. seismic and electromagnetic data), and these scales are usually not coincident to the subsurface simulation model scale. Alternatives like down/upscaling of the data and/or the simulation model can be used, but with potential loss of important information. To address this issue, a novel Multiscale (MS) data assimilation method is introduced. The overall idea of the method is to keep uncertain parameters and observed data at their original representation scale, avoiding down/upscaling of any quantity. The method relies on a recently developed mathematical framework to compute adjoint gradients via a MS strategy. The fine-scale uncertain parameters are directly updated and the MS grid is constructed in a resolution that meets the observed data resolution. The advantages of the technique are demonstrated in the assimilation of data represented at a coarser scale than the simulation model. The misfit objective function is constructed to keep the MS nature of the problem. The regularization term is represented at the simulation model (fine) scale, whereas the data misfit term is represented at the observed data (coarse) scale. The performance of the method is demonstrated in synthetic models and compared to down/upscaling strategies. The experiments show that the MS strategy provides advantages 1) on the computational side – expensive operations are only performed at the coarse scale; 2) with respect to accuracy – the matched uncertain parameter distribution is closer to the “truth”; and 3) in the optimization performance – faster convergence behaviour due to faster gradient computation. In conclusion, the newly developed method is capable of providing superior results when compared to strategies that rely on the up/downscaling of the response/observed data, addressing the scale dissimilarity via a robust, consistent MS strategy.Green Open Access added to TU Delft Institutional Repository ‘You share, we take care!’ – Taverne project https://www.openaccess.nl/en/you-share-we-take-care Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public.Reservoir EngineeringCivil Engineering & GeosciencesGeoscience and Engineerin

    A assistência social à população em situação de rua: um estudo na cidade de Florianópolis/SC

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    Tese (doutorado) - Universidade Federal de Santa Catarina, Centro de Filosofia e Ciências Humanas, Programa de Pós-Graduação em Sociologia Política, Florianópolis, 2015.O debate sobre a população em situação de rua (PSR) está presente no campo de ação das políticas públicas, porém poucas vezes se prioriza conhecer a percepção dessa população sobre os serviços que lhe são prestados e/ou garantidos. Este estudo objetivou compreender a percepção da PSR em Florianópolis acerca dos serviços de assistência social e verificar em que medida estes serviços correspondem ao que está previsto pelo Decreto nº 7.053/2009. Para desvelá-lo, realizou-se pesquisa qualitativa com levantamento bibliográfico acompanhada de pesquisa de campo tanto na rua, quanto nos espaços institucionais. Para critério de seleção da PSR entrevistada, priorizou-se a abordagem de maiores de 18 anos de ambos os sexos, acompanhados ou não pelo serviço municipal Centro de Referência ao seu atendimento, o Centro-Pop. Nos espaços institucionais profissionais dos serviços públicos municipais da assistência social (Centro Pop e Casas de Acolhimento/Abrigos); da saúde (Consultório na Rua e Centro de Atenção Psicossocial-CAPS); do Conselho Municipal de Assistência Social; assim como representantes de organizações não governamentais que atuavam com o atendimento a PSR foram ouvidos. As análises das respostas obtidas foram baseadas em sete categorias conceituais: status, estigma, fenômeno, rualização, pobreza, exclusão social e interdependência. Assim, verificou-se, sob a perspectiva da PSR, que estes não estão recebendo uma proteção social de forma integral; que há necessidade do investimento em ações que fortaleça a intersetorialidade da assistência social com as demais políticas públicas; que é importante valorizar o movimento de organização e participação política deste usuário; que as ações de intervenções com ele não asseguram relações interdependentes reificando a figuração de que indivíduo e sociedade são instâncias separadas. A partir disso, sugeriu-se uma metodologia de intervenção para com a PSR visando à construção de relações mais interdependentes entre eles e a sociedade.Abstract : The debate on the homeless population (HP) is present in the public policies field, but it seldom prioritizes know the perception of this specific group of people about the services that are provided and/or guaranteed for them. This study aimed to understand the perception of this population segment on the public service received by social assistance and if this service meets their needs as provided by Decree no. 7053 in Florianopolis. In order to reach this aim, a qualitative research was combined with both the field work on the street and in institutional space. For selection criteria of the HP interviewed, people over 18 years-old, both sexes, accompanied or not by the Reference Center - Centro-Pop, municipal service for their health care - were addressed. At the institutional space, professionals from the municipal public services of social assistance (Pop. Center and Refuge / Homeless Shelters); health workers (Office on the street and Psychosocial Care Center); the Municipal Council of Social Assistance; as well as representatives of non-governmental organizations (NGOs) who have been working with homeless care were heard. The responses analysis was based on seven conceptual categories: status, stigma, phenomenon, rualização, poverty, social exclusion and interdependence. The following findings were identified from the perspective of Homeless People: They are not being socially protected from a comprehensive health perspective; there is a need for investment in actions that strengthen the dialogue between social assistance and other public policies; it is important to enrich and incentive the organization of the Social Movement of this user; the intervention actions to them does not ensure an interdependent relationship, reifying the idea that individual and society are different instances. Based on that, this study has purposed an intervention methodology to HP in order to build interdependent relationships between them and the society

    Search for a low-mass pseudoscalar Higgs boson produced in association with a bb‾ pair in pp collisions at √s=8 TeV

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    A search is reported for a light pseudoscalar Higgs boson decaying to a pair of τ leptons, produced in association with a bb‾ pair, in the context of two-Higgs-doublet models. The results are based on pp collision data at a centre-of-mass energy of 8 TeV collected by the CMS experiment at the LHC and corresponding to an integrated luminosity of 19.7 fb−1. Pseudoscalar boson masses between 25 and 80 GeV are probed. No evidence for a pseudoscalar boson is found and upper limits are set on the product of cross section and branching fraction to τ pairs between 7 and 39 pb at the 95% confidence level. This excludes pseudoscalar A bosons with masses between 25 and 80 GeV, with SM-like Higgs boson negative couplings to down-type fermions, produced in association with bb‾ pairs, in Type II, two-Higgs-doublet models. © 2016 The Author(s

    Amblyseius victoireae Zannou, Moraes & Oliveira, n. sp.

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    Amblyseius victoireae Zannou, Moraes & Oliveira, n. sp. (Fig. 18) DIAGNOSIS—Seta Z 1 present; setae Z 5 much longer than distance between their bases; setae Z 4 and Z 5 smooth; ratios s 4:Z 1 = 11.3, s 4:S 2 = 10.1; seta j 3 ca. 1.4 as long as j 1. Ventrianal shield subpentagonal, smooth. Fixed cheliceral digit with 13 teeth. Genu of leg I with a macroseta; all macrosetae sharp-tipped. Spermatheca with calyx cup-shaped; atrium very small. FEMALE—(Specimens measured—Kenya: 4 and Uganda: 1. Idiosomal setal pattern 10 A: 9 B/JV- 3:ZV. Dorsum (Fig. 18 A)—Dorsal shield smooth, 354 (320–370) long and 259 (232–278) wide. Setae j 1 35 (32– 37), j 3 47 (42–51), j 4 6 (5–6), j 5 5 (3–8), j 6 6 (5–8), J 2 8 (8–10), J 5 6 (5–8), z 2 9 (6–11), z 4 7 (5–8), z 5 6 (3–8), Z 1 8 (8–10), Z 4 103 (94–109), Z 5 297 (272–317), s 4 91 (86–98), S 2 9 (8–11), S 4 9 (8–10), S 5 8 (5–10), r 3 10 (6–13), R 1 8 (6–10). Setae smooth. Peritreme—Extending beyond level of j 1. Venter (Fig. 18 B)—Sternal shield mostly smooth, with few lateral striae; posterior margin slightly concave; distances between St 1 -St 3 62 (59–66), St 2 -St 2 70 (66–74). Genital shield smooth; distance between St 5 - St 5 73 (70–80). Ventrianal shield smooth, subpentagonal, slightly constricted at level of preanal pores, anterior margin slightly convex, 122 (112–131) long, 83 (75–96) wide at level of Zv 2 and 73 (66–82) wide at level of anus; preanal pores elliptical, mesad and slightly posterior to Jv 2. Two pairs of metapodal shields. Chelicera (Fig. 18 C)—Movable digit 36 (35–37) long, with 3 teeth; fixed digit 31 (30–32) long, with 13 teeth and a pilus dentilis. Spermatheca (Fig. 18 D)—Calyx cup-shaped, 10 (8–11) long; atrium very small. Legs—Sharp-tipped macrosetae: Sge I 45 (43–46), Sge II 40 (37–43), Sge III 59 (51–64), Sti III 41 (38–43), Sge IV 131 (120–144), Sti IV 90 (86–96), St IV 74 (69–78); presence of a prominent erect seta at base of tarsus I. MALE—Unknown. LOCALITY AND TYPE MATERIAL—Holotype female from Combretum sp., 25 km S Malindi, Kenya, 11 -XII- 1989, J.S. Yaninek, deposited at ESALQ-USP; 1 paratype female from unknown plant, 25 km S Malindi, Kenya, 11 -XII- 1989, J.S. Yaninek, deposited at ESALQ-USP; 4 paratype females from Acacia brevispica, 25 km S Malindi, Kenya, 11 -XII- 1989, J.S. Yaninek, deposited at ESALQ-USP; 2 paratype females from unknown plant, Fedi Zuimi, Coastal Province, Uganda, 12 -XII- 1989, J.S. Yaninek, deposited at IITAIM; 1 paratype female from Theobroma cacao, 22 km N Bundibugyo, Uganda, 9 -X- 1990, J.S. Yaninek, deposited at IITAIM. ETYMOLOGY—This species is named in honor of Victoire O. Ahouantchessou Zannou, spouse of the first author of this paper. REMARKS— Amblyseius pretoriaensis Ueckermann & Loots, 1988 differs from this species by having j 3 ca. twice as long as j 1; Z 5 ca. twice and ca. 2.5 times as long as Z 4 and s 4, respectively; Z 4 and Z 5 serrate and atrium of spermatheca nodular. Amblyseius comatus Ueckermann & Loots, 1988 differs by having Z 4 and Z 5 serrate, ventrianal shield with transverse striae anteriorly to anus and macrosetae of leg IV with small knobs. Amblyseius haleakalus Prasad, 1968 differs from the new species by having j 3 about as long as j 1 and Sge IV ca. 1.3 times as long as St IV. Amblyseius kaguya Ehara, 1966 also differs by having j 3 ca. 1.5 times as long as j 1, Z 4 ca. 1.5 times as long as s 4 and Sge IV twice as long as St IV.Published as part of Zannou, Ignace D., De, Gilberto J., Ueckermann, Eddie A., Oliveira, Anibal R., Yaninek, John S. & Hanna, Rachid, 2007, Phytoseiid mites of the subtribe Amblyseiina (Acari: Phytoseiidae: Amblyseiini) from sub-Saharan Africa, pp. 1-47 in Zootaxa 1550 on pages 30-32, DOI: 10.5281/zenodo.17808
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