19,915 research outputs found

    Gordon B. Washburn and Mary K. Rubio, Radeke Garden, Museum of Art

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    Gordon B. Washburn and Mary K. Rubio in the Radeke Garden, Museum of Art.https://digitalcommons.risd.edu/archives_rubiocollection/1013/thumbnail.jp

    Crónica de la provincia de Málaga

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    Escudo xilográfico en portadaLas hojas de láminas: retratosEsc. xil. en portLas h. de lám.: retratosLas hojas de grabados son litografías: "Llanta, dib.\po\s y lit.\po\s¨ y ¨Lit. de Rubio, Grillo y Vitturi", retratos de Antonio Ríos Rosas, Cánovas del Castillo, Juan López Pinto, Joaquín de Eleta y José de Salamanca y el mapa es litogr.:"B. Cuaranta grab. lit\po\s", de la provincia de Málaga.Las h. de grab. son litogr.: "Llanta, dib.\po\s y lit.\po\s¨ y ¨Lit. de Rubio, Grillo y Vitturi", retratos de Antonio Ríos Rosas, Cánovas del Castillo, Juan López Pinto, Joaquín de Eleta y José de Salamanca y el mapa es litogr.:"B. Cuaranta grab. lit\po\s", de la provincia de Málag

    Rubio, B

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    Crónica de la provincia de Orense

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    As follas de láminas corresponden a retratos de personaxes que ilustran as obrasPort. propia de la seriePort. con esc xilAs 6 primeiras p. numeradas en romanosLa h. de map.: "B. Cuaranta grabs. litog\po\s". La h. de lám.: "Llanta dib\po\s y lit\po\s, lit. de Rubio y C\pia\s", retrato de Benito Gerónimo Feijo

    Salida de campo de José Manuel Rubio Recio a Sardón de Duero (Valladolid) el 28 de octubre de 1952

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    Salida de campo de José Manuel Rubio Recio a Sardón de Duero (Valladolid) el 28 de octubre de 1952, de la que el autor anotó observaciones sobre Lepus sp. (Liebre) y las siguientes aves: Aquila sp. (posiblemente, el Águila real, A.chrysaeos), Ardea sp. (Garza), Circus cyaneus (Aguilucho pálido), Corvus frugilegus (Graja), Coturnix coturnix (Codorniz común), Falco tinnunculus (Cernícalo vulgar), Garrulus glandarius (Arrendajo), Hieraaetus fasciatus (Águila perdicera) y Perdiz (Alectoris sp. o Perdix sp.).Field trip of José Manuel Rubio Recio to Sardón de Duero (Valladolid) the 28th of October of 1952, of which the author noted observations about Lepus sp. (Hare) and the following birds: Aquila sp. (possibly, the Golden Eagle, A.chrysaetos), Ardea sp. (Heron), Circus cyaneus (Northern Harrier), Corvus frugilegus (Rook), Coturnix coturnix (Common Quail), Falco tinnunculus (Common Kestrel), Garrulus glandarius (Eurasian Jay), Hieraaetus fasciatus (Bonelli´s Eagle) and Partridge (Alectoris sp. or Perdix sp.)

    Data supporting Rubio et al on exacerbations of COPD

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    Please see the publication Rubio et al. ('Home monitoring of breathing rate in people with Chronic Obstructive Pulmonary Disease: observational study of feasibility, acceptability and change after exacerbation' International Journal of Chronic Obstructive Pulmonary Disease, vol 2017:12. DOI: 10.2147/COPD.S120706) on exacerbations of COPD (chronic obstructive pulmonary disease)

    Myrmecotypus haddadi Perger & Rubio 2021, sp. nov.

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    Myrmecotypus haddadi sp. nov. ( LSID: urn:lsid:zoobank.org:act: 16B033D9-2AC3-415D-8741-B32C349CF7F0) Figs 2, 3, 4. Type material. Holotype ♂ from BOLIVIA: Santa Cruz department, Santa Cruz de la Colina, Urubo (-17.760833°; -63.24°), 432 m a.s.l., 21 Dec 2019, leg. R. Perger, Cerrado-like grassland adjacent to fragment of Chiquitano forest (ZMH-A0015356). Paratypes: 1 ♂, same data as holotype (ZMH-A0015357). 1 ♂, 1 ♀, Santa Maria la Antigua (- 17.3719°; -63.6563°), Cerradao, ~ 30 m away from Cerrado savanna, 13 Apr 2018, leg. R. Perger (IBSI-Ara1463). Etymology. The specific epithet, haddadi, is a patronym in honour of Charles R. Haddad in recognition of his contributions to the taxonomy of Castianeirinae. Diagnosis. Judging from the light coxa II and the remainder of coxae dark (Figs 2; 4B), the tibia I ventral spination 3-3 and the male genital bulb with two loops lateral to main sperm duct (Fig. 3 A-C), the species is most closely related to M. iguazu Rubio & Arbino, 2009, M. rubrofemoratus Perger & Rubio, 2021 and M. tahyinandu Perger & Rubio, 2020 (this combination of characters is not found in other congeners). Myrmecotypus haddadi sp. nov. can be separated from these species by a broader carapace in relation to the carapace length (carapace index of 57 in male and 54 in female) and the cephalic width (cephalic index of 67 in male and 70 in female) (Figs 2A, 4A, C); embolus of male palp cat claw-shaped, forming beak-like structure with a spatula-shaped tegular projection (coupling piece) (Fig. 3A, B), epigyne with two widely separated, rounded genital openings mediolateral to spermathecae (Fig. 3D, E) (see Tab. 1 for comparisons). Remarks. Rubio & Arbino (2009) and Perger & Rubio (2020a) hypothesized that some Neotropical species of Apochinomma Pavesi, 1881 may belong to Myrmecotypus. Amongst those species, A. formicoides Mello-Leitão, 1939, is the only with a sub-globose abdomen and light coxa II (the remainder of coxae dark) (Mello-Leitão 1939). This species can be distinguished from M. haddadi sp. nov. by a carapace index of 41 and the distance between the inner margins of the PLE being as wide as the maximum width of the AER (Mello-Leitão 1939) (wider in the new species). Description of male holotype. Body length 5.23; carapace length 2.79, width 1.58, carapace index 57; cephalic width 1.09, cephalic index 67; sternum length 1.28, width 0.93, sternum index 72; abdomen length 2.21, width 1.62, abdominal index 73; petiole length 0.09, width 0.38; dorsal sclerite length 2.21, width 1.62; epigastric sclerite length 0.63, width 1.07; ventral sclerite length 0.95, width 0.73; inframamillary sclerite length 0.23, width 0.56. AER 0.64; AME–AME 0.09; AME–ALE 0.04; PER 0.91; PME–PME 0.24; PME–PLE 0.17. Carapace (Fig. 2A, C). Obovate, squarely truncated anteriorly, front slightly convex, cephalic region narrowed, laterally slightly concave, thoracic region distinctly broadening in middle, evenly narrowing in posterior direction, posterior margin straight; slight constriction between cephalic and thoracic regions and posterior region strongly convex when viewed laterally. Dorsum weakly shiny, smooth, dark brown; setae short, appressed, white, simple, relatively dense laterally between cephalic and thoracic regions but not obscuring integument (setae mostly abraded after storage in ethanol). Eyes. Eight eyes in two rows; both slightly recurved, diameter of AME about 30% larger than that of other eyes. Chelicerae. Orange brown, shiny, glabrous, area between retro- and promarginal rows of cheliceral teeth orange white with dense white hairs, 2 retro- and 2 promarginal teeth. Abdomen. Short oval; anterior margin of petiole straight; dorsal sclerite completely covering abdomen dorsally and laterally; ventral sclerite fully developed, covering area between ventro-lateral margins of dorsal scutum and between epigastric and inframamillary sclerites; inframamillary sclerite narrow, subrectangular. Dorsum weakly shiny, smooth, dark brown; abdominal setae long, simple, not sclerotized to spines, dark; simple, short, white setae on abdomen; transverse band of feathery setae in middle; separate, long, erected white setae on posterior part (most setae strongly abraded). Legs. Coxa II translucent white, remainder of coxae dark brown, trochanters I-IV whitish-yellow; femora I and II translucent white, broad black bands along edges, remainder of leg I and II yellow; femora and tibiae III and IV dark brown, edges lined with bands of short, appressed, white feathery setae, base patella IV translucent white ventrally, metatarsi and tarsi III and IV light brown. Palp. Margin of pedipalp tibia continuous; tarsus with relatively broad genital bulb drawn out into broad neck, embolus cat claw-shaped, not twisted, forming beak-like structure with spatula-shaped tegular projection (coupling projection) (Fig. 3A, B); sperm ducts with two loops, both lateral and basal to embolus tube (Fig. 3A, B). Female paratype. Body length 4.4; carapace length 2.16, width 1.16; carapace index 53.7; cephalic width 0.81, cephalic index 70; sternum length 0.87, width 0.62, sternum index 71.3; abdomen length 2.12, width 1.59, abdominal index 75; petiole length 0.2; dorsal sclerite length 1.5, width 1.52; epigastric sclerite length 0.55, width 0.9; inframamillary sclerite length 0.2; width 0.4. AER 0.48; AME–AME 0.06; AME–ALE 0.02. PER 0.7; PME– PME 0.2; PME–PLE 0.12. Posterior part of carapace slightly convex when seen in lateral view (Fig. 4B), dorsal sclerite shorter than in male (Fig. 4B), 70% of abdomen length, posterior border slightly convex, ventral sclerite absent; remaining somatic characters as in male. Epigyne. With two widely separated, rounded genital openings mediolateral to spermathecae; two slight pouches (or furrows) posterior to each opening (maybe for fitting of male palpal projection) (Fig. 3D); separation between primary and secondary spermathecae slightly visible, primary and secondary spermathecae forming eggplantshaped spermathecae (Fig. 3E), copulatory ducts short, at level of copulatory openings, entering the spermathecae posteriorly. Variation. There was no visible intra-specific variation, except for that inherent in the gender dimorphism. Geographical and ecological distribution. This species is only known from the localities in Urubo and Santa Maria la Antigua, Santa Cruz department, Bolivia. In both localities, specimens were collected from low herbaceous plants in Cerrado-like vegetation along edges of Chiquitano and Cerradao forest (Fig. 1). In Urubo, M. haddadi sp. nov. was observed co-occurring with the Castianeirinae species Mazax cf. ramirezi Rubio & Danişman, 2014. Despite high sampling effort in several Bolivian forest ecoregions (Perger & Perger 2017; Perger & Rubio 2018, 2020a, b, 2021), the new species was not observed in forest habitats. Ant mimicry. In the other Bolivian species of Myrmecotypus, the color of body parts and the color and distribution of setae increases the resemblance to specific ant models of the tribes Camponotini or Dolichoderini (Perger & Rubio 2020a, 2021). Unfortunately, the life habitus of the new species was not documented and the loss of setae due to the storage in ethanol hampered the assessment of mimetic relationships. However, as in the other congeners, the body size, obovate carapace and short oval abdomen mostly resemble ants of Camponotini or Dolichoderini. Additional field observations are needed to identify potential ant models.Published as part of Perger, Robert & Rubio, Gonzalo D., 2021, Myrmecotypus haddadi sp. nov. - a new species of ant resembling sac spider from the Bolivian orocline (Araneae: Corinnidae: Castianeirinae), pp. 54-60 in Zootaxa 4969 (1) on pages 56-59, DOI: 10.11646/zootaxa.4969.1.2, http://zenodo.org/record/474585

    Análisis léxico de los Cuentos Inverosímiles de José López Rubio: entre lo real y lo inverosímil

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    Ilustración: "Niña en río"Este trabajo presenta un análisis lingüístico de los Cuentos Inverosímiles de José López Rubio, colección de veintiún cuentos publicada en 1924. Tras examinar los neologismos, los préstamos y los coloquialismos, es posible afirmar que en la obra se pone de manifiesto un contraste, intencional por parte del autor, entre los argumentos inverosímiles y el lenguaje, a veces real, a veces inverosímil. Este desajuste produce un original humorismo, el mismo que López Rubio expresó en sus posteriores piezas dramáticas y en toda su vida.This study approaches a linguistic analysis of Cuentos Inverosímiles by José López Rubio, a book including twenty-one histories published in 1924. After examining the neologisms, the borrowings and the colloquial language used by the author, one can affirm that in the work there is an intentional contrast between the inverosímiles contents and the way the author represents them, fluctuating between real and unreal expression. This contrast produces a special humour, the same that López Rubio expressed in his later plays and in his life

    Zoniopoda serrana Pocco, Rubio & Cigliano, 2011, n. sp.

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    <i>Zoniopoda serrana,</i> n. sp. <p>(Figs. 1A–D; 2A–I)</p> <p>Holotype male (http:// orthoptera.speciesfile.org/Common/basic/ShowImage.aspx?TaxonNameID=78162&ImageID=72737) and allotype female, ARGENTINA: Córdoba, La Falda, Cerro La Banderita (31º 04’ 48.23’’ S, 64º 27’ 31.28’’ W), 1419 m, 07/03/2010, M. Pocco, G. Rubio & M. Rubio, MLPA. Paratypes: 2 males, 1 female, ARGENTINA: Córdoba, La Falda, Cerro La Banderita (31º 04’ 48.31’’ S, 64º 27’ 31.67’’ W), 1418 m, 06/02/2010, G. Rubio, MLPA; 4 males, 6 females, Córdoba, La Falda, Cerro La Banderita (31° 04' 48.45" S, 64° 27' 42.69" W), 1300 m, 07/03/ 2010, M. Pocco, G. Rubio & M. Rubio, MLPA; 8 males, 1 female, Córdoba, La Falda, Cerro La Banderita (31º 04’ 48.23’’ S, 64º 27’ 31.28’’ W), 1419 m, 07/03/2010, M. Pocco, G. Rubio & M. Rubio, MLPA.</p> <p> <b>Etymology.</b> <i>Serrana</i> (Sp.), hill, referring to the distribution area in the Sierras Chicas of Córdoba. The gender is feminine.</p> <p> <b>Diagnosis.</b> Dorsal median carina of pronotum prominent, slightly granulate in lateral view, cut by deep transverse sulci (Fig. 2B). Male furculae set far apart and with rounded apex; epiproct with straight sides proximally and convergent at an obtuse angle distally (Fig. 2C). Body color greenish-yellow with light-blue (Figs. 1A–B, 2A); pronotal disk with wide yellow band along median dorsal carina and with two light greenish-yellow stripes along the lateral carinae; lateral lobes of pronotum with two yellow longitudinal bands along the middle area and the lower margin (Fig. 2B). Epiphallus with prominent subrectangular lophi (as seen from above) with oblique distal margin (Figs. 2F–I).</p> <p> <b>Description.</b> Integument rugose, except on top and postocular areas of the head, and on legs (Figs. 1A, 2A). Dorsal median carina of pronotum high, slightly granulate in lateral view, cut by three deep transverse sulci (Fig. 2B). Prozona slightly longer than metazona. Male abdominal terminalia (Fig. 2C) with furculae set far apart and with rounded apex; epiproct with straight sides proximally, and convergent at an obtuse angle distally. Male phallic complex (Figs. 2D–E) as in the remaining species of <i>Zoniopoda,</i> only differing in the shape of the epiphallus. Epiphallus with prominent subrectangular lophi (as seen from above) with oblique distal margins (Figs. 2F–I).</p> <p>Males: body color greenish-yellow with light-blue (Figs. 1A, 2A). Antennae black with yellow scape; each antennal segment with whitish distal end, in living specimens (Figs. 1A). Head greenish-yellow; antennal sockets, occiput and postgenae with spots of light-blue; fastigium, frontal costa and mouthparts with red markings. Pronotal disk light-blue with wide yellow band along median dorsal carina and two narrow light greenish-yellow stripes along lateral carinae; lateral lobes of pronotum with two yellow longitudinal bands, one along the middle area and the other one along the lower margin (Fig. 2B). Meso and metapleurae light-blue, with two oblique greenish yellow bands. Tegminae light-blue, with well marked yellow veins, especially the subcosta (SC), radius (R), second cubital (CuP) and anal veins. Hind wings with remigium greenish and vannus bluish. Fore and middle legs yellowish-green with red markings on coxae, tips of tibiae and tarsi; hind femora yellowish-green, outer face blue with light-blue pinnae, inner face with light-blue markings, rotular area pale red. Hind tibiae with inner face yellowishgreen and outer face greenish light-blue, tips of tibiae and tarsi bright red. Abdominal tergites light-blue, with an oblique yellow band near lateral edges. Terminalia (Fig. 2C): subgenital plate and cerci cream, furculae black, epiproct black with a median cream-colored band.</p> <p>Females (Fig. 1B): similar to males, but more robust. Ovipositor valves of soil-laying type, cream colored, with the tips dark red.</p> <p> <b>Measurements.</b> Body length: 34.5 mm (33–37) males, 45.6 mm (45–47) females; prozona length: 3.2 mm (2.95–3.42) males, 4.22 mm (3.95–4.41) females; metazona length: 3.05 mm (2.84–3.27) males; 4.2 mm (4.01– 4.48) females; hind femur length: 14.3 mm (13.5–15.5) males; 19.24 mm (18.5–20) females.</p> <p> <b>Relationships.</b> Based on the characters of pronotum and body color <i>Z. serrana</i> is included in the Iheringi species group that was shown to be monophyletic in the cladistic analysis presented herein. From the species that constitute the Iheringi group, <i>Z. serrana</i> is readily differentiated from <i>Z. similis</i> Bruner, the most similar species, by the following characters: antennae black; dorsal median carina of pronotum prominent; epiproct with straight sides convergent distally at an obtuse angle; male furculae set far apart and with rounded apex; pronotum with a wide yellow band along median dorsal carina, two narrow light greenish-yellow stripes along lateral carinae and two yellow longitudinal bands on lateral lobes; epiphallus with prominent subrectangular lophi (as seen from above) with oblique distal margin. Table 1 illustrates the differences between these species.</p> <p> The key! "# to the species of <i>Zoniopoda</i> based on Carbonell´s (2007) revision of the genus was modified and updated to include <i>Z. serrana</i> in the Orthoptera Species File online (http:// orthoptera.speciesfile.org/).</p> <p> <b>Distribution and habitat.</b> The species is known from Cerro La Banderita, in the Sierras Chicas mountain range, La Falda, Córdoba, Argentina (Fig. 1C), where individuals were found only above 1300 meters of altitude (see http:// orthoptera.speciesfile.org/Common/editTaxon/Distribution/SpecimensMap.aspx?TaxonNameID=75173 geographic distribution of the species group in the Orthoptera Species File). The vegetation consisted of tall grasses and herbaceous dicots (Fig. 1D). Below the mentioned altitude and in the other mountaintops surveyed from Sierras Chicas mountain range, only specimens of <i>Zoniopoda tarsata</i> were found.</p> <p> <b>1.</b> A, <i>Z. serrana</i> <b>n. sp.;</b> B, <i>Z. serrana</i> <b>n. sp.</b>; C, map; D, <i>Z. serrana</i>.</p> <p> <b>Cladistic analysis.</b> A parsimony analysis of the data matrix (Appendix 2) resulted in one most parsimonious tree of length 56 (consistency index, 0.85; retention index, 0.80) (Fig. 3). The analysis recovered <i>Zoniopoda</i> as a monophyletic group based on the following synapomorphies: union frons-fastigium angulated in lateral view (1:1) (Fig. 4 G); anterior margin of pronotum slightly projected over occiput (5:1) (Fig. 4 A); subgenital plate long with acute and bifurcate apex (11:1) (Fig. 4 J), with the highest support values. <i>Zoniopoda omnicolor</i> was shown to be the most basal species of the genus with the remaining species grouped into a clade supported by one synapomorphy (6:2, median dorsal carina of pronotum low throughout). Within this clade two groups were recovered: the first comprising <i>Z. tarsata</i>, <i>Z. danottei</i>, <i>Z. exilipes</i> and <i>Z. fissicauda</i> united by the epiproct rhomboidal with rounded edges (12:2); and the second comprising <i>Z. serrana</i> and the species of the Iheringi species group (<i>Z. similis</i>, <i>Z. mimicula</i>, <i>Z. hempeli</i>, <i>Z. iheringi</i> and <i>Z. juncorum</i>), supported by four synapomorphies: median dorsal carina of pronotum granulated or denticulate in lateral view (7:1) (Fig. 4 G); general coloration greenish, not mottled (19:1) (Fig. 4 A); color pattern of hind tibiae without bands, greenish and tips bright red (21:1) (Fig. 4 A); integument on metazona coarsely rugose, with upper parts of the rugae of same color (25:6) (Fig. 4 A). <i>Zoniopoda serrana</i> was recovered as sister-group to the rest of the Iheringi group which it shares a single synapomorphy (20:1, color pattern of body and hind femora uniformly green). Within the Iheringi group two clades were depicted, related by two synapomorphies (21:2, color pattern of hind tibiae without bands, salmon, light red or reddish; 22:3, color pattern of pronotum without bands), one clade comprising the sister taxa <i>Z. mimicula</i> and <i>Z. hempeli</i> supported by one synapomorphy (18:3, lophi of epiphallus prominent, subrectangular with pointed edges) and the other clade comprising <i>Z. iheringi</i> and <i>Z. juncorum</i> united by the integument of the metazona tuberculate (25:5).</p>Published as part of <i>Pocco, Martina E., Rubio, Gonzalo D. & Cigliano, Marta, 2011, A new species of Zoniopoda Stål (Orthoptera: Acridoidea: Romaleidae) from Argentina and its phylogenetic position within the genus, pp. 27-37 in Zootaxa 2913</i> on pages 28-33, DOI: <a href="http://zenodo.org/record/205562">10.5281/zenodo.205562</a&gt

    Crónica de la provincia de Cuenca

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    Port. con esc. xilTexto a dos colLas h. de lám.: retratosLas h. de grab. lit. son retratos de Gil de Albórnoz, Hernando de Alarcón, Melchor Cano y Fermín Caballero. La h. de mapa lit. es de Cuenca. Las il. litMapa de la provincia de Cuenca "B. Cuaranta grabo. lito." enfrentado a la port., y las h. de grab. : "Llanta dibo. y lito.", "Lit. de Rubio, Grilo y Vitturi", "V. Urrabieta, dibo. y lito.", "Lit. J. Donon. Madrid", "Lit. de Rubio y Cia.
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