226,534 research outputs found

    Penaincisalia elisabeth Prieto, sp. n.

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    Penaincisalia elisabeth Prieto, sp. n. (Figs. 1 A,B; 2 A,B; 3 A,B,C) Type material: Holotype 3 ICN: COLOMBIA, Boyacá, Sierra Nevada del Cocuy, Güicán, La Capilla, 3380m, 14 /01/ 2009, m 1095, C. Prieto Leg. Deposited in ICN-MHN. Paratypes: 2 3 CP: Colombia, Boyacá, Sierra Nevada del Cocuy, Güicán, La Capilla, 3380m, 13 /01/ 2009, C. Prieto Leg, m 1097, m 1094; 1 3 CP: Colombia, Boyacá, Sierra Nevada del Cocuy, Güicán, Monserrate, 3680m, 19 /01/ 2009, C. Prieto Leg, m 1096.; 1 Ƥ CP: Colombia, Boyacá, Sierra Nevada del Cocuy, Güican, La Capilla, 3380m, 15 /01/ 2009, C. Prieto Leg., m 1093.Published as part of Prieto, Carlos, 2010, Description of a new high Andean butterfly species (Lepidoptera: Lycaenidae: Theclinae) from the " Sierra Nevada del Cocuy ", Colombia, pp. 59-64 in Zootaxa 2506 on pages 60-61, DOI: 10.5281/zenodo.29421

    PRIETO, Manuel M.

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    Correspondence exchanged among Mr. Manuel M. Prieto, Manager of Customs in Ciudad Juárez, Chihuahua, Mr. Fernando Torreblanca, and Gen. Alvaro Obregón, regarding Gen. Obregón’s trip to El Paso, Texas and the Dallas, Texas Fair. / Correspondencia entre el Sr. Manuel M. Prieto, Administrador de la Aduana de Ciudad Juárez, Chih., el Sr. Fernando Torreblanca y el Gral. Alvaro Obregón, relativa al viaje del Gral. Obregón a El Paso, Texas, así como a la Feria de Dallas, Texas, E.U.A

    PRIETO, Manuel M.

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    Correspondence exchanged among Mr. Manuel M. Prieto, Manager of Customs in Ciudad Juárez, Chihuahua, Mr. Fernando Torreblanca, and Gen. Alvaro Obregón, regarding Gen. Obregón’s trip to El Paso, Texas and the Dallas, Texas Fair. / Correspondencia entre el Sr. Manuel M. Prieto, Administrador de la Aduana de Ciudad Juárez, Chih., el Sr. Fernando Torreblanca y el Gral. Alvaro Obregón, relativa al viaje del Gral. Obregón a El Paso, Texas, así como a la Feria de Dallas, Texas, E.U.A

    ¡Traiga el palito y cantamos! Everyday life, experiences, and representations of the affective musical practices of the Prieto Monroy family

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    Este estudio busca comprender la configuración de las prácticas musicales en la cotidianidad de la familia Prieto Monroy. La investigación implicó observar los nodos y la redes entre actores, lugares y espacios, objetos y acciones; identificar patrones y rutinas de escucha, habla e interpretación; y analizar de forma compleja las prácticas musicales de la familia. El estudio de caso alrededor de la música que acontece con y en la familia Prieto Monroy se plantea como una investigación de tipo micro social que aborda el espacio privado, escrita en primera persona. Así, pretende interpelar y ser un punto de perspectiva y reflexión sobre cómo se ha entendido la práctica musical desde los estudios culturales y las ciencias sociales. A través de la teoría del actor-red y el giro afectivo, la tesis presenta el concepto de prácticas musicales afectivas entendidas como una configuración de relaciones de actores, espacios y lugares, acciones y objetos que suceden con y a través de la música como fenómeno sonoro. El ensamblaje social que presenta el caso de la familia Prieto Monroy puede mostrar las relaciones y nodos entre agencias conectadas (Latour, 2013), como también es un reflejo de un compendio de emociones y conocimientos que pasan a través del cuerpo y la intersubjetividad (Wetherell, 2012). Los datos se recogieron a través de entrevistas semiestructuradas; observación, participación y entrevista etnográfica; recopilación de fotografías familiares y videos familiares; y la reflexión los recuerdos propios de la investigadora. Los resultados que presenta esta investigación se establecen en 3 vías principales: la reconstrucción de la historia familiar vista desde el lente de la música, la comprensión de las prácticas entendidas como prácticas musicales afectivas, y la presentación de una perspectiva metodológica que incluye las vivencias propias de la investigadora y que tiene la posibilidad de ser un aporte para las investigaciones musicales desde el eje de la vida cotidiana y el espacio privado. Por lo tanto, el trabajo está constituido con base en el cruce de las trayectorias familiares y la música en la vida cotidiana de cuatro generaciones. Esto se aborda por medio de la noción de los grooves generacionales, que sirven como puntos focales para la comprensión de gustos, prácticas musicales, y usos de lo material a través del tiempo. Adicionalmente, se expone una interpretación de la vida cotidiana en la que se analizan los afectos, las prácticas musicales dentro de la familia, el espacio de la vivienda y sus relaciones, las tecnologías, los instrumentos musicales y la música misma; todo esto de manera compleja. Para ello se apela al análisis de las relaciones entre seres humanos y materialidad, por medio de la idea de la resonancia, la cuál es el resultado de un trabajo de mediación entre lo natural y lo cultural, lo local (música en la vida privada) y lo global (música institucional). (Texto tomado e la fuente)This study aims to understand the configuration of musical practices in the everyday life of the Prieto Monroy family. The research involved observing the nodes and networks among actors, places and spaces, objects, and actions; identifying patterns and routines of listening, speaking, and interpretation; and conducting a complex analysis of the family's musical practices. The case study revolving around music that occurs with and within the Prieto Monroy family is proposed as a microsocial research conducted within the private sphere, written in the first person. Thus, it intends to challenge and provide a perspective and reflection on how musical practice has been understood from cultural studies and social sciences. Through the actor-network theory and the affective turn, the thesis introduces the concept of affective musical practices, understood as a configuration of relationships among actors, spaces and places, actions, and objects that occur with and through music as a sound phenomenon. The social assemblage presented by the case of the Prieto Monroy family can reveal the relationships and nodes among connected agencies (Latour, 2013), as well as reflect a compilation of emotions and knowledge that pass through the body and intersubjectivity (Wetherell, 2012). Data was collected through semi-structured interviews; observation, participation, and ethnographic interviews; collection of family photographs and family videos; and the reflection on the researcher's own memories. The results presented by this research are established in three main analisys pathways: the reconstruction of family history seen through the lens of music, the understanding of practices as affective musical practices, and the presentation of a methodological perspective that includes the researcher's own experiences and has the potential to contribute to musical research from the perspective of everyday life and private space. Therefore, the work is based on the intersection of family trajectories and music in the everyday life of four generations. This is addressed through the notion of generational grooves, which serve as focal points for understanding tastes, musical practices, and the use of material over time. Additionally, an interpretation of everyday life is presented in which affections, musical practices within the family, the living space and its relationships, technologies, musical instruments, and music itself are analyzed; all of this in a complex mode. This involves the analysis of relationships between humans and materiality, through the idea of resonance, which is the result of a mediation between the natural and the cultural, the local (music in private life) and the global (institutional music).MaestríaMagisterEtnografí

    PRIETO, Manuel M. (Col.)

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    Correspondence of Col. Manuel M. Prieto from the Administration of the Fiscal Stamp in Monterrey, Nuevo Leon, Gen. Alvaro Obregón, and Mr. Fernando Torreblanca, in which Gen. Alvaro Obregón thanks the former for his willingness to work in support of his candidacy. Mr. Fernando Torreblanca sends some coopies of the MANIFESTO TO THE NATION by Gen. Alvaro Obregón. / Correspondencia entre el Corl. Manuel M. Prieto de la Administración del Timbre de Monterrey, N.L., el Gral. Alvaro Obregón y el Sr. Fernando Torreblanca, en las que el Gral. Obregón agradece al primero su disposición por trabajar en apoyo a su candidatura. El Sr. Fernando Torreblanca envía algunos ejemplares del MANIFIESTO A LA NACION del Gral. Alvaro Obregón

    PRIETO, Manuel M. (Col.)

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    Correspondence of Col. Manuel M. Prieto from the Administration of the Fiscal Stamp in Monterrey, Nuevo Leon, Gen. Alvaro Obregón, and Mr. Fernando Torreblanca, in which Gen. Alvaro Obregón thanks the former for his willingness to work in support of his candidacy. Mr. Fernando Torreblanca sends some coopies of the MANIFESTO TO THE NATION by Gen. Alvaro Obregón. / Correspondencia entre el Corl. Manuel M. Prieto de la Administración del Timbre de Monterrey, N.L., el Gral. Alvaro Obregón y el Sr. Fernando Torreblanca, en las que el Gral. Obregón agradece al primero su disposición por trabajar en apoyo a su candidatura. El Sr. Fernando Torreblanca envía algunos ejemplares del MANIFIESTO A LA NACION del Gral. Alvaro Obregón

    Proceedings of the 6th Gesture and Speech in Interaction Conference / Encouraging gesture use in a narration task increases speakers gesture rate, gesture salience and the production of representational gestures

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    Previous work has shown the positive effect of encouraging gestures in performing varioustasks; in these studies, the participants generally appeared to gesture more when explicitlyasked to do it. However, little attention has been paid to whether encouraging gestures alsoaffects other gesture features, i.e., gesture type and salience. In this paper we explore this issue.Twenty native Italian speakers described the content of short comic strips to a listener in 2conditions: Non-Encouraging gestures (N); Encouraging gestures (E). Co-speech gestures weremanually coded and classified according to gesture type (Representational vs. Non-Representational) and gesture salience (Salient vs Non-Salient). The results show thatinstructing speakers to gesture led to an increase in gesture rate, in gesture salience, and in thenumber of representational gestures. By contrast, in the non-encouraging condition the rate ofNon-Salient gestures was significantly higher, but no difference was found for Non-Representational gestures.Alice Cravotta, Pilar Prieto and M. Grazia Bus

    Rhamma dawkinsi Prieto & Lorenc-Brudecka 2017, sp.nov.

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    Rhamma dawkinsi PrieTo & Lorenc-Brudecka sp.nov. (Figures 3, 4, 10, 11, 12) Type material. Holotype male: COLOMBIA, Antioquia, Belmira, Páramo de Belmira, 3100 m, 05/01/2011, specimen number: RCCP m1309, CP Lep 0 0 99, GWOTI669-12; BOLD:ABX0547; C. Prieto Leg. The holotype is deposited in ICN-MHN. Paratypes: 3 ♂ RCCP: COLOMBIA, Antioquia, Belmira, Páramo de Belmira, 3100 m, 05/01/2011, specimen numbers: m1303, m1304, m1307; C. Prieto leg.; 2 ♂ RCCP: COLOMBIA, Antioquia, Belmira, Páramo de Belmira, 3100 m, 02/08/2015, specimen numbers: m1872, m1871; C. Prieto leg.; 3 ♀ RCCP: COLOMBIA, Antioquia, Belmira, Páramo de Belmira, 3100 m, 05/01/2011, specimen numbers: m1305, m1306, m1308, C. Prieto leg. This new species belongs to Rhamma shares the following combination of characters with all other species of Rhamma: 1) androconial scent brand appearing as an elongate streak bordering the upper vein of the discal cell apex on DFW (Fig. 3); 2) male genitalia with vinculum forming a 90 degree angle basally (Fig. 10); 3) vinculum strut strongly developed (Fig. 10); 4) ductus bursae short, robust, and with strongly developed lamella postvaginalis terminating in serrate, or multi-pronged configurations (Fig. 12); 5) fan shaped and dendritic signa (Fig. 12); 6) ductus bursae in dorsal or ventral aspect lightly sclerotized in the middle so that it appears to be transparent (Fig. 12); and 7) a ventral element associated with the 8th tergite in female genitalia (figure 3:C, J in Johnson 1992). Diagnosis. Rhamma dawkinsi appears to be a sibling species of the sympatric R. adunca as both have a very similar ventral wing pattern. Rhamma dawkinsi differs from R. adunca (Figs. 1, 2) in having a smaller anal lobe and a longer and thinner androconial cluster. Additionally, R. dawkinsi is consistently smaller than R. adunca, and the upper margin of the hindwing turns down less abruptly than in R. adunca. Genital structures are practically indistinguishable (Figs. 7, 8, 9) as in the most of the species in the genus. Description. Adult male wings. Mean forewing length 10.9 mm (measured from forewing apex to base at thorax); n = 3. Hindwing anal angle pointed, without tail at vein Cu2. Dorsal wing surface homogeneous silverblue, except for black margin extending from postmedial region of forewing and very narrow black margin (1–2 mm) on hindwing. No apparent orange scaling in anal angle. Ventral forewing surface gray with two thin, straight lighter lines (Figs. 3, 4). Conspicuous white band crossing medial area of ventral hindwing from costa to vein Cu2. Androconial cluster appearing as an elongate streak bordering ¼ of upper vein of discal cell apex on DFW. Etymology. This species is named after the eminent English ethologist, evolutionary biologist, and popularizer of Science, Richard Dawkins, for his contributions to the public understanding of evolution and his fight against irrational thinking. Biology. Males land on vegetation 1–2 m above the ground in the páramo-high Andean forest ecotone. Males appear to establish mating territories in the early afternoon around 1330 hours on the sunny edges of paths or on ridge tops. The spatial separation and the distance from the ground of the perching places of this species show a clear segregation from the individuals of R. adunca that fly on the same hilltops. Rhamma dawkinsi prefers small isolated bushes (1–2 m high) where males stay for a few minutes before leaving for another bush in a combination of perching and patrolling behaviour, whereas R. adunca males perch on leaves of small trees 4–5 m high. The immature stages, larval food plants, and adult nectar sources are unknown. Adults were captured in January and August. Distribution. The species is known only from the type locality, Páramo de Belmira in the central mountain range of the Colombian Andes, at 3100 m elevation (Fig. 15). Remarks. Differences in size, wing pattern, and behaviour, as well as sympatry with the absence of intermediate individuals between both phenotypes and molecular comparisons, combine to show that R. adunca and R. dawkinsi, sp. n., are closely related, but different species. Although associating the sexes of many Eumaeini is difficult, Rhamma dawkinsi has a restricted geographical range and the wing pattern is almost identical in both sexes. Molecular diagnostic characters. The intraspecific haplotype diversity in the available sequences (n = 3) was Hd = 3. Overall mean distance among the available sequences is 0.30%, maximum intraspecific distance is 0.31%. The lowest overall mean distance to another member of the genus is 2.98% to R. comstocki (eastern cordillera). The molecular diagnostic characters when compared with the most similar species based on morphology are in the Figure 14. A guanine in the position 453 of the mtDNA gen COI is diagnostic for this new taxon when compared with the 13 species recorded in Colombia by Prieto & Vargas (2016).Published as part of Prieto, Carlos & Lorenc-Brudecka, Jadwiga, 2017, Description of Rhamma dawkinsi (Lepidoptera: Lycaenidae) a new mountain butterfly from Colombia, pp. 587-594 in Zootaxa 4338 (3) on pages 588-593, DOI: 10.11646/zootaxa.4338.3.12, http://zenodo.org/record/103696

    Lamprospilus bicolor Faynel & Prieto 2023, sp. nov.

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    Lamprospilus bicolor Faynel & Prieto, sp. nov. (Figures 9–12, 17, 25, 32) Type material. Holotype male: COLOMBIA, Valle del Cauca, Alto Aguacatal, Cerro Brisas, 1970 m, 12/06/2005, C. Prieto. The holotype is currently deposited in RCCP (specimen number: m518). Paratypes (n = 29): 10 males, RCCP: same locality as the holotype, 5–25/08/2005, specimen numbers: m463, m465, m479, m526, m527, m535, m556, m480, m481, m482, C. Prieto; 4 males, RCCP: COLOMBIA, same locality as the holotype, 1950 m, 08/09/2018, specimen numbers: m2486, m2487, m2488, m2489, C. Prieto; 4 males, RCCP: COLOMBIA, Valle, Alto Aguacatal, La Elvira, 1900 m, 1–10/08/2018, specimen numbers: m2342, m2358, m2356, m2357, C. Prieto; 1 male, RCJFLC: COLOMBIA, Cerro Aguacatal, Quinchía, Risaralda, 15/05/1997, 1600 m, J. Salazar leg.; 2 males, HNHM: Cerro Ingrumá (Municipio de Ríosucio), hilltop 2270 m, 3 pm, 29/07/1994, Salazar leg.; 3 males, HNHM: same locality as the holotype, 6 and 22/08/2005, Prieto leg.; 2 females, RCCP: COLOMBIA, Valle, Alto Aguacatal, La Elvira, 1900 m, 1,5/08/2018, specimen numbers: m2359, m2351, C. Prieto; 1 female, RCCP: same locality as the holotype, 1850 m, 6/08/2018, specimen number: m2370, C. Prieto. 1 female, HNHM: Valle: R. Aguacatal, S. Antonio, 2280 m, 2003.VI. 10, Dahners leg.; 1 female, HNHM: Valle: R. Cali, El Faro, 1700 m, 10/02/2005, Dahners leg. Description. Male: Wings. Forewing average costal length measured from wing base to apex 16.6 mm (n = 25); hindwing with a short black tail with white tip at end of vein CuA 1, and with an additional, three times longer, tail at end of vein CuA 2; dorsal forewing surface deep blue, fading to black towards the apex, dorsal forewing marginal area black and 2.2 mm wide; dorsal hindwing surface deep blue with a 1 mm black marginal area, anal fold grey and a minute orange spot at tornus. Ventral forewing surface with two tones of greyish brown, three white lines crossing the wing, discal cell crossed by a small basally incurved white line reaching sub-costal vein (Sc), a second medial white line continuous from Sc to CuA 2 and deeply dislocated towards the base from CuA 2 to 2A, a third more diffuse white submarginal line from R 2 to CuA 2; entire area between CuA 2 and 2A on ventral forewing with a clear greyish blue suffusion; ventral hindwing surface with two tones of greyish brown, and three white lines crossing the wing, the first postbasal from Sc to the basal vein of the discal cell, the second in the medial area forming the typical “W”-shaped pattern of the Theclinae, and the third sub-marginal. Black cubital spot surrounded by red-orange scales in CuA 1 -CuA 2 accompanied by another small black spot at tornus (Figure 9). Male genitalia: Brush organs dense and dark, well developed tooth in the middle of the gnathos. Slender saccus rectangular in shape (Figure 17). Female: Wings. Forewing average costal length measured from wing base to apex 15mm (n = 3); hindwing with a short black tail with white tip at the end of CuA 1, and with an additional tail, three times longer, at the end of CuA 2; dorsal forewing surface bright blue, turning to black towards apex, marginal area black and 2.2 mm wide; dorsal hindwing bright blue with a 1.3 mm wide black marginal area, anal fold grey with a minute orange spot at tornus. Ventral forewing surface lustrous grey, three white lines crossing the wing, discal cell crossed first by a small straight one, the second a continuous medial from R 1 to CuA 2 and deeply dislocated and arrowhead-shaped from CuA 2 to 2A, and the third submarginal from R 2 to 2A; ventral hindwing grey with three white cross lines, the first postbasal from Sc to the discal cell basal vein, the second medial, forming the typical “W”-shaped Theclinae band, and third submarginal; black cubital spot surrounded by red-orange scales in CuA 1 -CuA 2 (bigger than in males) accompanied by another small black spot at tornus (Figure 10). Adult female body: Thorax and abdomen covered with brown and dark gray scales. Female genitalia: See diagnosis and Figure 25. Etymology: The specific epithet refers to the two tones of the ventral color of both male wings. It comes from the Latin word “bicolor” treated here as a masculine adjective in the nominative singular. Biology. Males appear to display their main activity around mid-day from 12:00–14:00 hours on trees 4–6 m high in forest clearings. Females were captured visiting isolated bushes or patrolling clearings and paths inside the forest. The immature stages, larval food plants, and adult nectar sources are unknown. Adults were captured during the months of May, June, August and September. Diagnosis. Males of L. bicolor sp. nov. can be differentiated from those of L. coelicolor (Butler & H. Druce, 1872) and L. aunus (Cramer, 1775) in lacking a dark brown patch at the base of the ventral hind- and forewings and by having three well defined white lines in the ventral fore and hindwing surfaces (see Figures 13, 15). Females of L. bicolor sp. nov. and L. coelicolor (Figures 10, 12) are almost indistinguishable and different tonalities of grey in ventral surface could be shared in the wide distributional range of this species. When dissections of males are compared, brush organs are much denser and longer in L. bicolor sp. nov., than in L. coelicolor (Figures 17, 18). L. aunus has no brush organ (Figure 19). Molecular diagnostic characters and BINs. Nine intraspecific haplotypes were found in the available sequences of L. bicolor sp. nov. (n = 20). Haplotype diversity was higher in Colombian populations. The lowest overall mean distance to another member of the genus is 3.81% to L. coelicolor from Pastaza, Ecuador. Two BINs were associated to this new species in BOLD systems; BOLD:ACV4947 for the Colombian specimens and BOLD:ACP8506 for the Peruvian specimens. The maximum intraspecific distance was 4.03%. Diagnostic fixed states and their position in the COI barcode sequence are: a cytosine in position 100 of the COI Gen (Figure 27). Distribution. L. bicolor sp. nov. has been found in Colombia in the valleys of the Aguacatal, Calima and Pance rivers at altitudes between 1900 and 2100 m in Valle del Cauca, and in Quinchía, in Risaralda (Figure 32). Remarks. This species has been collected regularly for the last 20 years on the eastern slopes of the western mountain range near the city of Cali, Colombia, however it was first considered as a montane form of L. coelicolor (Prieto & Dahners 2006). New distributional data and the sequencing of the COI gene barcode region of a good series of specimens allow us to reject the hypothesis of conspecificity with L. coelicolor and consider it as valid species because of the following reasons: 1. The wide distribution of L. bicolor sp. nov. (Colombia, Peru, Bolivia) is not consistent with a hypothesis of a clearly defined geographic subspecies of L. coelicolor. 2. If the two forms of L. bicolor sp. nov. (from Colombia and Peru) were considered two different parapatric subspecies of L. coelicolor in each country, each subspecies would be genetically closer to individuals of L. coelicolor from populations in its own region. However, L. bicolor sp. nov. from Colombia is closer to L. bicolor sp. nov. from Peru than to L. coelicolor from Colombia. This suggests genetic cohesion and reproductive isolation throughout the geographic distribution of L. bicolor sp. nov. (Figure 26).Published as part of Prieto, Carlos, Faynel, Christophe & Lorenc-Brudecka, Jadwiga, 2023, Integrative description of two new species and two new subspecies of Lamprospilus Geyer (Lepidoptera: Lycaenidae), pp. 145-159 in Zootaxa 5244 (2) on pages 149-151, DOI: 10.11646/zootaxa.5244.2.3, http://zenodo.org/record/765605

    M. Nieto Ibáñez – J. M. Torres Prieto (eds.), Historia de la literatura cristiana en la Antigüedad

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    M. Nieto Ibáñez – J. M. Torres Prieto (eds.), Historia de la literatura cristiana en la Antigüedad. Madrid: Editorial Ciudad Nueva. Colección Estudios Patrísticos 2024. ISBN: 978-84-9715-577-9 [Por Anselmo Matilla Santos
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