210,749 research outputs found
Reseña de Casas Gómez, M. (dir.), Paredes Duarte, Mª J. y Varo Varo, C. (eds.) (2005). VIII Jornadas de Linguística.
No full textSe trata de una reseña de Casas Gómez, M. (dir.), Paredes Duarte, Mª J. y Varo Varo, C. (eds.) (2005). VIII Jornadas de Linguística
Heliura fenestrifer Duarte 2017, comb. nov.
No full textHeliura fenestrifer (Zerny, 1931), comb. nov. (Figs. 6, 24–28) Ptychotrichos fenestrifer Zerny, 1931: 254. Ptychotrichos fenestrifer; Pinheiro & Gaal-Haszler, 2015: 511 Ptychotrichos fenestrifer; Pinheiro & Gaal-Haszler, 2015: 511, fig. 8. Diagnosis. Vertex, dorsal surface of thorax, patagia, tegulae and forewings with grayish-green and brown scales, the latter also with white scales rendering a hyaline appearance where they occur. Post-occiput with small light yellow spots. Hindwings partially hyaline. Discal cell open. Dorsal surface of abdominal tergites roseate, except for T7–8, brown with the posterior margin roseate and white, respectively. S2–4 brown with laterals white. Remaining sternites entirely brown. Material examined (2 ♂ and 1 ♀ ). BRAZIL: Maranhão , Açailândia, 4°56'49"S 47°30'17"W, 19–27.xi. 1990, 150m, V. O. Becker & G. S. Dubois, 76650 (VOB), 1 female; Pará, Santarém, Fazenda Taperinha, 2°26'22"S 54°41'55"W, v.1920, C. Hagmann (NHMW) (holotype); PERU: Pasco , Pan de Azúcar, 10°20'11"S 75°50'38"W, 8.vii.1961, F. S. Truxal (LACM), 1 male; idem, LRP404, 1 male. Remarks. This species belongs to Heliura excavata species group (sensu Pinheiro & Duarte 2016). This group was originally defined by the peculiar hindwing shape exhibited by its members, H. excavata (Dognin, 1910), H. perexcavata (Rothschild, 1912), and H. juliani Pinheiro & Duarte, 2016. Even though H. fenestrifer comb. nov. does not have acute angles in the hindwings as in the other species in the group, they all share a highly peculiar hindwing venation (fig. 6), plus several characters of male genitalia, such as a long and thin saccus, and subdivided valvae with a dorsal highly sclerotized portion, and a ventral, slightly sclerotized portion. As in P. zeus, the wide distribution of H. fenestrifer comb. nov. raises doubt that a single taxon has such a wide distribution. However, the rarity of specimens of this group in collections and the lack of possibility to barcode old museum specimens have prevented the examination of the number of taxa involved in what we are here calling H. fenestrifer comb. nov.Published as part of Duarte, Marcelo, 2017, Revision of the Neotropical moth genus Ptychotrichos Schaus (Lepidoptera, Erebidae, Arctiinae, Arctiini, Ctenuchina), pp. 246-258 in Zootaxa 4312 (2) on pages 255-256, DOI: 10.11646/zootaxa.4312.2.2, http://zenodo.org/record/85279
Duarte Lobo: Asperges me
No full textPreview of the edition of Portuguese composer Duarte Lobo's (c.1566-1646) antiphon "Asperges me" for four voices (SATB) from the 1621 Liber Missarum. Polyphonia 23 Work is fully available at http://www.mpmp.pt/produto/polyphonia-23-duarte-lobo-asperges-m
Método sem malha hp-clouds na análise de placas Reissner-Mindlin /
No full textDissertação (Mestrado) - Universidade Federal de Santa Catarina, Centro Tecnológico.O conteúdo deste trabalho trata da aplicação do método sem malha hp-Clouds ou simplesmente método de nuvens (C. A. Duarte e J. T. Oden [8]) à solução de problemas de placas de Reissner-Mindlin
Duarte Lobo: Vidi aquam
No full textPreview of the edition of the antiphon "Vidi aquam" for four voices (SATB) by Portuguese composer Duarte Lobo (c.1564-1646) from the 1621 Liber Missarum. Polyphonia 26
Data for "Modeling the potential impact of viral load monitoring on vertical transmission of HIV in Kenya"
No full textSimulated data in .csv format on the impact of viral load testing on the following outcomes for two HIV+ maternal cohorts, a Newly Positive Cohort and a Known Positive Cohort: proportions of each cohort virally suppressed overall and by treatment status, and cumulative numbers of births, deaths and vertical transmissions. A codemap translating simulation time step to maternal event time is also included.These data contain the output of our HIV microsimulation model of disease progression, HIV care and vertical transmission among pregnant women living with HIV in Kenya. The data can be used to reproduce Figures 2-4 and Supplementary Figures and Tables in Duarte et. al 2025.Eunice Kennedy Shriver National Institute of Child Health and Human Development- DP1HD115428NIAID- K01AI157841Minnesota Population Center (Award Number P2CHD041023, parent funder Eunice Kennedy Shriver National Institute of Child Health and Human Development)PhRMA Foundation Health Outcomes Research Starter GrantDuarte, Horacio A; Birnbaum, Jeanette K. (2026). Data for "Modeling the potential impact of viral load monitoring on vertical transmission of HIV in Kenya". Retrieved from the Data Repository for the University of Minnesota (DRUM), https://doi.org/10.13020/EEZS-KV14
The marriage record of Noras, Santos C. and Gonzalez, Mirendes Duarte
No full textMarriage license for Santos C. Noras and Mirendes Duarte Gonzalez. J.C. Sale was the officiant
Gibboryctes endroedii Duarte and Grossi 2022, sp. nov.
No full textGibboryctes endroedii Duarte and Grossi, sp. nov. (Figures 3; 6 (c); 7(c); 8(c); 9(b); 10 (c,d); 11(c); 12(e,f); 13(c); 14(b)) Diagnosis Gibboryctes endroedii differs from other Gibboryctes species by the following combination of characters: body colouration reddish brown or dark reddish brown (Figure 3); labrum subtrapezoidal with broadly rounded apex (Figure 6 (c)); maxillae with lobed galea and stipe with a triangular lateral lobe (Figure 8 (c)); pronotal sides almost completely covered with large and coalescent punctures (Figure 12 (e)); elytral interstriae densely covered with large punctures (Figure 12 (f)). Type material Holotype male dissected, labelled: (a) ‘ Brasil, Minas Gerais, Lavras/Poço Bonito, 20.xi.2012 / 1060 m, Grossi & Parizotto /criação ninhos de cupim’ [white label]; (b) ‘ Gibboryctes endroedii sp. nov. / HOLOTYPE / Duarte & Grossi det. 2021’ [red label] (CERPE). Two males and two females paratypes with same data as holotype (CERPE). Two female paratypes, labelled: (a) ‘ Brasil, Minas Gerais, Ingaí / iii.2008, termiteiro chão/Vaz-de-Mello, ab. larva’ [white label]; (CERPE). One female paratype, labelled: (a) ‘ Brasil, Minas Gerais, Ingaí / xi.2007, breed, Vaz-de - Mello leg’. [white label]; (CEMT). One male paratype, labelled: (a) ‘ Brasil, Rio de Janeiro / Itatiaia, I.1947, A. Englir’ [white label]; (CERPE). Paratypes with a yellow paratype label. Holotype description Male (Figure 3). Length : 24.6 mm. Width: 11.7 mm. Colour: Nearly completely reddish brown; protibial teeth black. Head: Clypeus triangular, transverse, 2 times wider than long, acuminate anteriorly, weakly narrowed laterally; lateral margin slightly raised; surface rugose, densely setose on sides separated by a glabrous middle area. Frontoclypeal suture with a transverse, flattened, short, subtrapezoidal tubercle. Frontal surface glabrous, transversely rugopunctate; punctures large, coalescent, C-shaped; interocular width equals 4.1 transverse eye diameter. Ocular canthus transverse, subtriangular, glabrous, with a small notch at lateroposterior outer corner. Mouthparts: Labrum subtrapezoidal, broadly rounded on apical margin (Figure 6 (c)). Mandibles with 2 teeth on outer margin; apical tooth subtriangular; basal tooth subrectangular, rounded apically, clearly larger in size compared to apical tooth (Figure 7 (c)). Maxillary galea lobed, widely rounded at apex (Figure 8 (c)); inner margin with 3 subapical teeth increasing in size towards apex; apical and basal teeth triangular; medial tooth lobed; inner margin rounded just below basal tooth; stipe expanded laterally in triangular shape (Figure 8 (c)). Maxillary palpomere II 1.6 times longer than width at middle. Labium subtriangular, slightly rounded laterally, becoming narrow towards apex; surface densely punctate; sides densely covered with long bristles; disc with scarce bristles, shorter than lateral compared to lateral bristles. Thorax: Pronotum rounded laterally in dorsal view, weakly convex in lateral view, longitudinal middle area slightly concave; anterior area with a small tubercle separated from anterior border by a deep groove; posterior pronotal border incomplete; pronotal surface almost entirely covered with ocellate punctures (Figure 9 (b)); punctures on sides deep, large, predominantly coalescent; longitudinal pronotal mid-line with a row of coalescent punctures; posterior areas on each side with shallow punctures scattered about 2 diameters of punctures. Scutellar plate subtriangular, scarcely punctate; punctures small, confined to anterior area. Elytra with 9 well-marked striae (1 sutural, 4 discal, 4 lateral); striae covered with a row of ocellate, deep, oval punctures; discal striae with contiguous punctures, gradually becoming smaller and sparser (about 1 diameter of punctures) towards posterior area; lateral striae with punctures scattered about 2 diameters of punctures, smaller compared to the discal striae; interstriae with punctures irregularly scattered, with mixed large and fine punctures. Legs: Mesotibial outer carinae with 11 stout spinules like setae (3 on basal carina, 8 on medial carina). Metatibia with 16 stout spinules like setae (6 on basal carina, 10 on medial carina). Abdomen: Tergite VIII with glabrous surface, strongly rugopunctate on lateral corners, densely punctate on discal area; punctures large, deep, from coalescent to contiguous on sides, becoming scattered about 1 diameter of punctures on disc. Ventrites I–VI rugopunctate on sides, finely punctate on discal area; ventrites II–V with an incomplete row of setigerous punctures near to posterior margin; ventrite VI glabrous, emarginate posteriorly at middle. Aedeagus: Parameres, in dorsal view, wide at basal half, becoming convergent towards a narrow apical half, covered with scarce bristles on inner edge of apex (Figure 10 (c)). Parameres, in lateral view, arched dorsally, ventrally with a longitudinal carina at middle, apex rounded, strongly constricted dorsoventrally (Figure 10 (d)). Variation Male paratypes. Length: 21.1–29.4 mm; Width: 11.0– 11.1 mm. As for holotype except the dark reddish brown colour; frontoclypeal tubercle bilobed; mandibles with lobed apical teeth; maxillae with 4 teeth at inner margin of galea; parameres widely divergent at basal half in dorsal view and with straight ventral surface in lateral view. Female paratypes. Length: 21.0– 23.37 mm; Width: 10.9–11.3 mm. As holotype except by the clypeus slightly rounded anteriorly (Figure 11 (c)); pronotum densely punctate compared to males (Figures 11 (c) and 12(e)); tergite VIII slightly convex in lateral view; ventrite VI parabolic, lacking posterior emargination (Figure 13 (c)). Etymology The specific epithet ‘ endroedii ’ is a homage to Dr Sebö Endrödi, author of the genus Gibboryctes and one of the greatest experts on Dynastinae in the twentieth century. Geographic distribution (Figure 14 (b)) Brazil (Minas Gerais, Rio de Janeiro). Remarks Gibboryctes endroedii sp. nov. resembles G. szelenyii in the reddish-brown body colour and elytral interstriae densely covered with punctures mixed among small and shallow, and large and deep. Besides this, males of G. endroedii have variations in the shape of parameres that sometimes overlap those observed in G. szelenyii. However, G. endroedii sp. nov. is clearly distinct by the labrum parabolic in shape; maxillary galea rounded at apex with all teeth located subapically on the inner margin; anterior corners of pronotum covered with large and coalescent punctures. Gibboryctes szelenyii have triangular labrum; triangular maxillary galea with all teeth located at middle of inner margin; anterior corners of pronotum with contiguous punctures or spaced about 1 diameter of punctures. Identification key to adults of Gibboryctes Endrödi 1. Body with dark reddish-brown or reddish-brown colouration (Figures 1; 3). Frons rugopunctate in female (Figure 11 (a,b)). Juxtasutural interstriae with large and dense punctures scattered from anterior to posterior elytral area (Figure 12 (b,f))................. 2 - Body with black colour (Figure 2a). Frons punctate in female (Figure 11 (b)). Juxtasutural interstriae with large punctures scarce and confined to anterior elytral area (Figure 12 (d)). Male unknown.. Gibboryctes ebeninus Duarte and Grossi sp. nov. 2. Labrum subtrapezoidal, with broadly rounded apex (Figure 6 (c)). Galea broadly rounded at apex (Figure 8 (c)). Punctures on the anterior pronotal corners predominantly coalescent (Figure 12 (e))......... Gibboyctes endroedii Duarte and Grossi sp. nov. - Labrum subtriangular (Figure 6 (a)). Galea triangular (Figure 8 (a)). Punctures on the pronotal corners predominantly contiguous (Figure 12 (a))..................................................................................................................................................................... Gibboryctes szelenyii Endrödi Notes on natural history of Gibboryctes Specimes of Gibboryctes szelenyii and G. endroedii sp. nov. were collected inside of epigeous termite nests (Blattodea:Isoptera: Termitidae). Gibboryctes szelenyii was found to be associated with many termite species (see remarks under G. szelenyii). Termites were not collected from the nests where specimens of G. endroedii were found. The localities of nests are marked by shrub vegetation and rocky outcrops characteristic of open areas of savannah and rupestrian grasslands (Figure 15 (a,b)). Adults, pupae and larvae of G. szelenyii and G. endroedii sp. nov. were found occupying the central portion of nests (Figure 16 (a–d)). When handled, the larvae emitted a stridulation sound produced by friction among the mandibles and maxillae. Furthermore, the larvae were observed building rigid galleries structured with faeces and saliva.The pupal chamber is also quite rigid,perhaps to avoid termite attacks (Figure 16 (c)).The larval excrement, when dried, acquires a peculiar aspect similar to ‘pellets’, flattened and subrectangular, with almost straight corners (90-degree angles),and which can be considered a diagnostic character for generic identification. This discovery represents the first record of an Oryctini associated with a termite nest. Regarding G. ebeninus sp. nov., only adults were collected, in an area under a Eucalyptus crop where a Pennsylvania light trap was installed, which perhaps attracted the specimens. Identification key to adults of Gibboryctes Endrödi 1. Body with dark reddish-brown or reddish-brown colouration (Figures 1; 3). Frons rugopunctate in female (Figure 11 (a,b)). Juxtasutural interstriae with large and dense punctures scattered from anterior to posterior elytral area (Figure 12 (b,f))................. 2 - Body with black colour (Figure 2a). Frons punctate in female (Figure 11 (b)). Juxtasutural interstriae with large punctures scarce and confined to anterior elytral area (Figure 12 (d)). Male unknown.. Gibboryctes ebeninus Duarte and Grossi sp. nov. 2. Labrum subtrapezoidal, with broadly rounded apex (Figure 6 (c)). Galea broadly rounded at apex (Figure 8 (c)). Punctures on the anterior pronotal corners predominantly coalescent (Figure 12 (e))......... Gibboyctes endroedii Duarte and Grossi sp. nov. - Labrum subtriangular (Figure 6 (a)). Galea triangular (Figure 8 (a)). Punctures on the pronotal corners predominantly contiguous (Figure 12 (a))..................................................................................................................................................................... Gibboryctes szelenyii Endrödi Notes on natural history of Gibboryctes Specimes of Gibboryctes szelenyii and G. endroedii sp. nov. were collected inside of epigeous termite nests (Blattodea:Isoptera: Termitidae). Gibboryctes szelenyii was found to be associated with many termite species (see remarks under G. szelenyii). Termites were not collected from the nests where specimens of G. endroedii were found. The localities of nests are marked by shrub vegetation and rocky outcrops characteristic of open areas of savannah and rupestrian grasslands (Figure 15 (a,b)). Adults, pupae and larvae of G. szelenyii and G. endroedii sp. nov. were found occupying the central portion of nests (Figure 16 (a–d)). When handled, the larvae emitted a stridulation sound produced by friction among the mandibles and maxillae. Furthermore, the larvae were observed building rigid galleries structured with faeces and saliva.The pupal chamber is also quite rigid,perhaps to avoid termite attacks (Figure 16 (c)).The larval excrement, when dried, acquires a peculiar aspect similar to ‘pellets’, flattened and subrectangular, with almost straight corners (90-degree angles),and which can be considered a diagnostic character for generic identification. This discovery represents the first record of an Oryctini associated with a termite nest. Regarding G. ebeninus sp. nov., only adults were collected, in an area under a Eucalyptus crop where a Pennsylvania light trap was installed, which perhaps attracted the specimens.Published as part of Costa, Leidiane O., Duarte, Paulo R. M., Iannuzzi, Luciana & Grossi, Paschoal C., 2022, Taxonomic revision and notes on natural history of the enigmatic beetle genus Gibboryctes Endrödi (Coleoptera: Melolonthidae: Dynastinae), pp. 191-225 in Journal of Natural History 56 (1 - 4) on pages 212-214, DOI: 10.1080/00222933.2021.2017499, http://zenodo.org/record/675831
Duarte Lobo: Magnificat Secundi Toni (versos pares)
No full textPreview of the edition for the even verses of the "Magnificat Secundi Toni by Portuguese composer Duarte Lobo (c.1564-1646). For four (SATB), three (ATB) and six (SSAATB) voices. Polyphonia 25 Work is fully available at http://mpmp.pt/produto/polyphonia-25-duarte-lobo-magnificat-secundi-toni-versos-pares
Bothynus araya Duarte & Grossi 2020, new species
No full textBothynus araya Duarte & Grossi, new species (Figs. 5 A–F; 7B; 8E; 9E; 10D, F; 12E) Diagnosis. Both sexes of B. araya are similar to B. entellus; however B. araya can be distinguished using the following characters: stridulatory apparatus with well-marked carinae near to basal margin in both sexes (Fig. 7B); parameres with lateral “flaps” distinctly as narrow as basal half (Fig. 8E); female differ from the females of other species in this group by the pronotum with weakly punctate concavity and smooth discal area (Fig. 10D) and proventrite with a long furrow at anterolateral angles (Fig. 10F). Etymology. The specific epithet is named as tribute to the grandmother of the first author. The name “araya” originates from the Tupi-Guarani dialect, meaning “grandmother”. This name should be treated as a noun in apposition. Type material. Holotype not dissected. Brasil: Paraná: Guarapuava, 3.IV.2012, Oliveira. G.B. – 1♂ (CERPE). Paratypes [16 males and 2 females]. One male and one female with same data as holotype (CERPE). Brasil: Minas Gerais: Poços de Caldas, XI.1995,— 1♂ (YPC). Paraná: Castro, Estrada Castro-Tibagi, Km 15, 15.XII.2006, P. Grossi & Parizotto— 1♂ (EPGC). Brasil: Santa Catarina: Campos Novos, (27º23’S, 51º12’W), II.2011, armadilha pitfall, R.C. Campos—(1♂ MAHC, 5♂ 1♀ CERPE, 4♂ CEMT). Paraguay: Caaguazú: Sommerfeld, I.1962 — 1♂ (MAHC). No data —(1♂ CERPE, 1♂ YPC). Description. Holotype male (Fig. 5A). Body l ength: 25.0 mm. Body width: 14.0 mm. Color: Dark brown. Head: Clypeus subpentagonal in shape, moderately punctate, weakly setose on sides, strongly constricted laterally at apical half, basal half with parallel and slightly raised sides. Frontoclypeal suture with a weak ridge interrupted at middle, nearly reaching the lateral margins. Interocular width equals 2.8 transverse eye diameters, frontal surface weakly rugopunctate, sides scarcely setose, basal area between eyes smooth. Eye canthus subquadrate. Mouthparts: Mandibles bidentate, teeth subtriangular. Mentum subtriangular, convex at disc, weakly rounded and densely covered with setose punctures on sides, disc smooth. Maxilla with quadridentate galea; 1 apical tooth (strong), 2 medial teeth (1 weak, 1 strong), 1 basal tooth (weak). Pronotum: Moderately convex, without horns, only with 1 small, conic-shaped apical tubercle; concavity V-shaped, shallow, confined to anterior area (Fig. 5A), hypomeron convergent (Fig. 5D); surface finely punctate Scutellar shield: Triangular in shape, smooth. Elytra: Surface with barely marked longitudinal striae, finely punctate, only observed under 90X magnification. Legs: Inner protarsal claw dilated, protarsomere IV with short ventral apex (Fig. 5E). Mesofemora with setae confined on disc (Fig. 5F). Mesotibiae slightly convex on external surface. Abdomen: Ventrites I–IV completely setose, V setose only on sides, VI bordered with setae on apex. Tergite VII with stridulatory apparatus formed by a band of transversal carinae well marked on the basal area, becoming finely marked toward the apical area (Fig. 7B). Tergite VIII with weak, setose punctures confined to sides, disc smooth. Variation. Male paratypes differ from holotype in the following aspects: Body length: 21.0– 26.5 mm. Body width: 11.0–13.0 mm. Color: Pronotal and elytral surface with variation from dark reddish brown to reddish brown. Pronotum: Concavity occasionally small and shallow compared to holotype, sometimes U-shaped. Aedeagus: Parameres in caudal view (Fig. 8E), middle area abruptly constricted on sides, apical half expanded in shape of subparallel lateral “flaps”, as narrow as the basal half. In lateral view, apex downcurved (Fig. 9E). Female paratypes (Fig. 5B) differs in the following aspects: Body length: 21.0– 26.5 mm. Body width: 11.0–13.0. Pronotum: Concavity rounded, small, confined near to anterior margin; latero-anterior surface moderately punctate, concavity weakly punctate, disc smooth (Fig. 10D). Legs: Protarsus not thickened, claws simple. Venter: Proventrite with a long furrow at anterolateral angles (Fig. 10F). Abdomen: Ventrite VI triangular shaped, not emarginate apically. Tergite VIII flattened in lateral view. Geographic distribution. Brazil: Minas Gerais, Paraná, Santa Catarina. Paraguay: Caaguazú (Fig. 12E). Bothynus araya occurs in open fields predominantly characterized as having shrubby vegetation within the “Campos Gerais” region from southern Brazilian to Paraguay.Published as part of Duarte, Paulo R. M. & Grossi, Paschoal C., 2020, Bothynus entellus (LePeletier & Serville) (Coleoptera: Scarabaeidae: Dynastinae) species group: taxonomic revision and description of two new species, pp. 101-121 in Zootaxa 4750 (1) on pages 111-113, DOI: 10.11646/zootaxa.4750.1.5, http://zenodo.org/record/370286
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