3,560 research outputs found
FIGURE 2 in Anatomical redescription of Aplysia (Aplysia) nigra and Aplysia (Varria) inca (Mollusca: Heterobranchia) with comments on Aplysia from Peru
No full textFIGURE 2. Distribution of Aplysia nigra and Aplysia inca. Type localities indicated by stars.Published as part of Mendivil, Alejandro & Cardoso, Franz, 2022, Anatomical redescription of Aplysia (Aplysia) nigra and Aplysia (Varria) inca (Mollusca: Heterobranchia) with comments on Aplysia from Peru, pp. 201-239 in Zootaxa 5222 (3) on page 203, DOI: 10.11646/zootaxa.5222.3.1, http://zenodo.org/record/746149
New records of teratology in Chiton cumingsii and Chiton granosus (Mollusca: Polyplacophora) from the Peruvian coast
No full textCardich-Becerra, Luz, Mendivil, Alejandro, Cardoso, Franz (2023): New records of teratology in Chiton cumingsii and Chiton granosus (Mollusca: Polyplacophora) from the Peruvian coast. Papéis Avulsos de Zoologia 63: 1-12, DOI: 10.11606/1807-0205/2023.63.036, URL: https://www.revistas.usp.br/paz/article/view/20897
The blind spots of secularization
No full textAccording to several international surveys Spain is among the western countries with the most negative views of Jews. While quantitative data on the topic accumulates, there is a significant lack of interpretative approaches that might explain the particular Spanish case. This paper presents the background, methodology and major results of a discussion group-based study on antisemitism, which was conducted in Spain in the autumn of 2009. The study identifies and locates in different socio-economic and ideological milieus the range of stereotypical discourses on Jews, Judaism and the Arab–Israeli conflict in Spain. Analysis of the group meetings shows that, despite growing secularization in Spanish society, the central explanatory variable for persisting and resurging antisemitism in this country is still religion in a broad cultural sense.N
Aplysia (Varria) inca d'Orbigny 1837
No full textAplysia (Varria) inca d’Orbigny, 1837 (Figures 18–32) Aplysia inca d´Orbigny, 1837: 207–209, pl. 19, figs. 1–3; Alamo & Valdivieso 1997: 84; Uribe et al. 2013a: 47. ? Aplysia chierchiana Mazzarelli & Zuccardi, 1889: 52; Mazzarelli & Zuccardi, 1890: 52; Alamo & Valdivieso 1997: 83; Nakamura 2006: 79; Uribe et al. 2013a: 47. Tethys inca — Pilsbry, 1895: 87, pl. 19, figs. 29–31. ? Tethys chierchiana — Pilsbry, 1895: 87. Aplysia (Varria) inca — Eales, 1960: 321; Paredes et al. 1999b: 31; Ramírez et al. 2003: 264; Nakamura 2006: 79. Type material. Syntype, 1 dissected individual, deposited at MNHN, Paris (Valdés & Héros 1998). Type locality. Between Callao and San Lorenzo Island, Peru (d’Orbigny 1837). Material examined. PERU, Piura: Sechura (Matacaballo), 1 specimen 60 mm length, 17.I.2004 (LaBSIM 15.06-0013). PERU, La Libertad: Huanchaco, 1 specimen 110 mm length, 21.III.2018, J. Esplana col. (LaBSIM 15.06-0034). PERU, Ancash: Samanco, 3 specimens 113–149 mm length, 1992, V.H. Vera col. (LaBSIM 15.06- 0006), 3 specimens 70–80 mm length, 6.III.1996 (LaBSIM 15.06-0009). PERU, Lima: Ancón, 1 specimen 70 mm length, 9.X.1977, C. Paredes col. (LaBSIM 15.06-0002.1), 2 specimens 63–106 mm length, 5.II.1993, C. Paredes col. (LaBSIM 15.06-0007), 3 specimens 58–80 mm length, 10.IV.1995, J. Quesada col. (LaBSIM 15.06-0008), 1 specimen 96 mm length, 27.IX.1997, C. Paredes col. (LaBSIM 15.06-0010), 1 specimen 79 mm length, 26.IX.1999, C. Paredes col. (LaBSIM 15.06-0011), 1 specimen, 83 mm length; 8.XII.2000, F. Cardoso col. (LaBSIM 15.06- 0042), 1 specimen 91 mm length, 8.XII.2000, F. Cardoso col. (LaBSIM 15.06-0012), 1 specimen 101 mm length, 2. VI.2017, F. Cardoso col. (LaBSIM 15.06-0020.1), 2 specimens 66–102 mm length; 17. VI.2017, F. Cardoso col. (LaBSIM 15.06-0022), 3 specimens, 19.XI.2017, P. Guardales & J. Leandro col. (LaBSIM 15.06-0027.1-3), 1 specimen 185 mm length; 7.IX.2018 (LaBSIM 15.06-0038). PERU, Callao: La Punta (La Arenilla), 2 specimens 161–177 mm length, 6.XII.2000, F. Cardoso col. (LaBSIM 15.06-0044). PERU, Lima: Barranco, 16 specimens 87–186 mm length, 15.I.2018, A. Mendivil col. (LaBSIM 15.06-0032). PERU, Lima: Chorrillos, 4 specimens 136– 146 mm length, 16.IX.2017, A. Mendivil col. (LaBSIM 15.06-0025), 6 specimens 115–186 mm length, 5.XI.2017, A. Mendivil col. (LaBSIM 15.06-0026), 5 specimens 136–199 mm length, 9.XII.2017, A. Mendivil col. (LaBSIM 15.06-0028), 1 specimen 84 mm length, 10.I.2018, A. Mendivil col. (LaBSIM 15.06-0031). PERU, Lima: Pucusana, 2 specimens 149–151 mm length, 11.XII.1977 (LaBSIM 15.06-0004), 1 specimen 40 mm length, 1983 (IMARPE 04-001902), 1 specimen 179 mm length, 2017, C. Cisneros col. (LaBSIM 15.06-0017), 3 specimens 147–205 mm length, 16.XII.2017, A. Mendivil & A. Bravo col. (LaBSIM 15.06-0029.1-3), 2 specimens 222–233 mm length, 6.I.2018, A. Mendivil col. (LaBSIM 15.06-0030.1-2). PERU, Ica: Paracas, 1 specimen 64 mm length, IV.2017, P. Carbajal col. (IMARPE 04-001901). PERU, Ica: Laguna Grande, 1 specimen 77 mm length, 6. V.1984, C. Paredes col. (LaBSIM 15.06-0005), 1 specimen 108 mm length, 24.XII.1998, C. Paredes col. (LaBSIM 15.06-0043.1). Description External morphology. Size ~ 230 mm in length. Color variable, purple, reddish, or dark green, with or without white or yellow spots, sometimes aggregated in dense concentrations, specially between anterior end of parapodia and rhinophores, posterior internal margin of parapodia and dorsal mantle (Figs. 18, 19); parapodia edge sometimes lighter than body color; mantle papilla sometimes with fine radial lines (Fig. 21). Body soft, elongated, relatively high, narrowing gradually towards cephalic region (Fig. 20A). Cephalic tentacles elongated, thick, enrolled, with narrower bases, forming oral veil (Fig. 20A: tc). Oral lobes located on ventral surface of oral veil (Figs. 20A–B: lo). Rhinophores conical, thick, close together. Foot sole relatively narrow, thick, with pair of lobes poorly differentiated in propodium, with narrow and elongated metapodium, sometimes developed in pointed tail (Fig. 20C). Parapodia broad, widely open, joined low down posteriorly, joined anteriorly with lobes slightly developed in anterior margin of parapodia (Figs. 20A–B: lpa). Visceral hump relatively large, oval, elevated, well differentiated, occupying more than 1/3 of body length (Fig. 20A). Mantle foramen reduced to elevated papilla, located on center of mantle (Fig. 20A, 21A, 21D: arrow). Anal siphon wide, elongated, tubular, occupying ~1/3 of mantle length, freely exposed within parapodial cavity (Fig. 22). Opaline gland resembling a bunch of grapes, with large, rounded main opening surrounded by many very small secondary openings, occupying small area on pallial cavity floor (Figs. 20A: oa, 21B–C, 21E–F: arrows). Opaline gland secretion milky white. Ink gland secretion purple, copious. Shell. Relatively large, shell length more than 1/3 of body length, width/length ratio about 3:4, arched, rounded to oval, relatively broad, wider close to anal sinus; on apertural view left margin slightly convex; right margin convex, narrowing gradually towards apex, anal sinus relatively narrow, usually concave (Fig. 23). Protoconch in apex of calcified layer. Sculpture formed by very fine concentric lines. Haemocoel organs. Haemocoel of A. inca very similar to A. nigra (Fig. 24), except for the grape-shaped opaline gland on dorsal wall of haemocoel, occupying a very small fraction of haemocoel volume (Figs. 21C, 21F: arrow). Circulatory and excretory systems. Arrangement of circulatory and excretory systems very similar to A. nigra (Fig. 25). Digestive system. Digestive system of A. inca similar to A. nigra, as described above, except for the following: Jaws thin, without longitudinal ridges, ~2 times wider than long, anterior and posterior borders smooth (Fig. 26A), with elongated jaw elements, sometimes knobbed, slightly curved toward distal end, tip narrower with a longitudinal slit (Fig. 26B–D). Dorsal folds less developed than in A. nigra (Fig. 26E: arrows), with elongated palatal elements, curved toward distal end, tip narrower (Figs. 26F–G). Odontophore muscles: m1x, pair of auxiliary jugal muscles, ~10 times longer than wide (Figs. 27A, 27C); m2, pair of strong retractor muscles of buccal mass, relatively thin, ~15 times longer than wide (Figs. 27A–C); m7, pair of very narrow and thin muscles, ~20 times longer than wide (Fig. 27I). Pair of odontophore cartilages forming radular bolsters narrow and slightly elevated (Fig. 27I: oc). Radular formula 48 x 1.19.1.17.1 (specimen length: 66 mm, LaBSIM 15.06-0022.2), to 67 x 2.40.1.40.2 (specimen length: 130 mm, LaBSIM 15.06-0032.5). Rachidian tooth bilaterally symmetrical, wider om base, with small, triangular central cusp with 2 small denticles on each side, 1 small secondary cusp on each side of central cusp, lacking secondary cusps (Fig. 28: black arrow). Lateral teeth asymmetrical, elongated, with large and triangular main cusp with up to 4 denticles on each side, 1 secondary cusp well developed with up to 2 additional smaller cusps distally (Fig. 28: white arrow). Marginal teeth small, with vestigial cusp. Pair of salivary glands ducts thin, cylindrical, equal in width along their length (Figs. 29 A-B, 30H: sg). Crop subdivided in two chambers of similar volume (Figs. 29 A-B). Gizzard presenting 10-11 large, pyramidal chitinous plates of rhomboid base, distributed in 3 transverse rows occupying posterior region of gizzard (Figs. 29B, 30A–D); presenting up to 20 small, conical chitinous plates of oval to circular base, usually distributed in a single row occupying anterior region of gizzard (Figs. 29B, 30A, 30E–F). Filter chamber occupying 1/3 of gizzard volume, presenting many small, conical gastric hooks distributed in several irregular transverse rows forming a relatively narrow band (Figs. 29B, 30A, 30G). Digestive caecum running embedded within digestive gland along most of its length, tip wide and flattened (Figs. 29A, 29C, 30I: ca); typhlosole continuing into intestine for about 1/3 of stomach length. Intestine slightly convoluted (Fig. 29C). Reproductive system. Penial sheath well differentiated into proximal penial canal and distal penial sac (Fig. 31A). Penial canal elongated, with muscular, thick wall, highly folded (Figs. 31B–D: pl). Penial sac bulbous, with thin wall, unarmed (Figs. 31B–D: ps). Penis thin, elongated, ~12 times longer than wide, unarmed; with triangular, rounded tip (Fig. 31E), seminal groove ending on longer side of tip, opposite side thinner (Figs. 31B–D). Pair of retractor muscles of penis thick, ~10 times longer than wide (Fig. 31A: mr). Protractor muscles of penis formed by many thin fibers (Fig. 31A: mp). Hermaphrodite reproductive system of A. inca like A. nigra, except for the following: Preampullary duct wide, about same width as ampulla, slightly curved. Ampulla thick, strongly convoluted, leading to very narrow postampullary duct (Fig. 31F: am). Large hermaphroditic duct relatively narrow, cylindrical, curved, but not convoluted as ampulla, ~2 times wider than ampulla, slightly attached to dorsal inner surface of haemocoel (Fig. 31F: lh). Nervous system. Nervous system of A. inca very similar to A. nigra (Fig. 32), except for the following: Cerebral ganglia fused forming single mass, slightly wider than pedal ganglion. Nerves leaving pedal ganglia (Fig. 32D): pd5, slender, bifurcating into 2 branches: pd5a, arrangement very similar to A. nigra; pd5b, inserting into lateral anterior body; pd5c not observed. Cerebropleural connectives slightly asymmetric, right connective slightly longer than left one. Pleural ganglia almost same size. Pleurovisceral connectives ~1 1/2 times longer than nerve ring length. Geographic distribution. Sechura, Piura (5° S) to Laguna Grande, Ica (14° S), Peru. Habitat and ecology. Sandy beaches, tidal pools, rocky shores with algae; intertidal to subtidal. Mass mortality events seem to be more common than in A. nigra. Apparently more abundant than A. nigra. Remarks. D’Orbigny (1837) described A. inca as a moderately elongated, tall animal; color purple, covered with white rounded spots; with parapodia well developed joined low down posteriorly, and anal siphon elongated and wide (Fig. 1B). Eales (1957, 1960) examined the type material of A. inca adding to the original description a penial sheath unarmed; penis broad, short, pointed at the tip; and opaline gland partly compound with a group of openings arranged in a circle. The specimens examined here are consistent with the original description of A. inca and the observations of Eales (1957, 1960), except for the shape of the penis which is generally elongated rather than broad and short as stated by Eales (1957, 1960). Although A. inca has been the most reported species of the subgenus Varria in Peru (Eales 1960, Paredes et al. 1988, Paredes et al. 1999a, Ramírez et al. 2015), during the nineteenth century two other species were also described for the Peruvian coast: Aplysia lessonii Rang 1828 and Aplysia chierchiana Mazzarelli & Zuccardi, 1889; however, currently only A. inca is considered a valid species (MolluscaBase 2021). Aplysia lessonii was described from Paita, northern Peru, as rounded, tall animals, grayish pink with very fine red markings, parapodia joined posteriorly and wide anal siphon (Rang 1828, fig. 1A). Mazzarelli & Zuccardi (1890) reported A. lessonii for Honolulu, Hawaii as animals with a large mantle foramen, feature not mentioned by Rang (1828). Kay (1964) reported five species of Aplysia for the Hawaiian Islands, but there was no mention of A. lessonii. Since none of the species described by Kay (1964) nor those reported later for Hawaii (Golestani et al. 2019: A. elongata) are consistent with the original description of A. lessonii, and we did not find a subsequent record of this species for the northern Pacific, the record of A. lessonii for the Hawaiian Islands should be considered probably erroneous. D’Orbigny (1837) distinguished A. inca and A. lessonii using the external coloration and morphological traits such as parapodia, mantle and cephalic tentacles; however, as Rang (1828) described A. lessonii on the basis of preserved specimens, the differences noted by d’Orbigny (1837) between the two species are questionable. Eales (1960) could not examine the type material of A. lessonii deposited at MNHN, Paris (1 syntype dissected, see Valdés & Héros 1998); but she concluded that by similitudes in body shape, foot, parapodia, mantle and shell, it could be a junior synonym of A. keraudreni Rang (1828) from the southwest Pacific. Aplysia keraudreni is a rather large dark brown animal, covered with white spots and a fine black reticulum (Eales 1960, Willan & Morton 1984); originally described from the Society Islands in the Polynesia, but also reported from New Zealand (Eales 1960, Willan 1979, Willan & Morton 1984, Morley & Hayward 2015) and Australia (Nimbs 2017a). Since the external coloration of A. keraudreni is not consistent with the description of A. lessonii (Rang 1828) nor with that reported in another species from the Eastern Pacific (Pilsbry 1895, Eales 1960, Beeman 1968, Bebbington 1977, Behrens & Hermosillo 2005, Camacho-García et al. 2005, Valdés 2019), A. keraudreni is very likely restricted to the southwest Pacific. Therefore, the records of A. keraudreni for Peru (Eales 1960, Bebbington 1977, Paredes et al. 1999 b, Ramírez et al. 2003, Nakamura 2006, Uribe et al. 2013a) should be considered erroneous. Until the examination of the material type of A. lessonii can corroborate the similitudes between both species, we decide to retain the name of A. inca for the typical species of the subgenus Varria in Peru. Mazzarelli & Zuccardi (1889) introduced the name of A. chierchiana for a dark animal, with black rounded spots and small white dots, wide parapodia, mantle foramen reduced to a small papilla, and opaline gland compound and multiporous; suggesting the mantle papilla as the diagnosis feature of this species (Fig. 1E). Although Mazzarelli & Zuccardi (1890) considered A. chierchiana very distinct from A. inca, with both having the same type locality, Eales (1960) did not compare them and rejected the name A. chierchiana, without specifying whether due to lack of type material, or by an inadequate description. In this work, we found that the most characteristic feature of A. chierchiana are the black rounded spots that cover the body of the living animals, not described in A. inca (d’Orbigny 1837, Eales 1960). Specimens that can be identified as A. chierchiana were found in Sechura, Samanco and San Lorenzo Island; where A. inca specimens have also been observed, with both species similar in body shape, foot, anal siphon, mantle papilla, shell, radula, jaws, and penis. Although A. chierchiana is included here as a probable synonym of A. inca, these specimens are not included in the anatomical redescription of A. inca until their taxonomic status is clarified using molecular data. Uribe et al. (2013a, b) recorded A. juliana for Máncora, Isla Santa (Samanco), Ancón and Paracas. However, these animals have parapodia joined low down posteriorly and release purple ink, characteristics not reported in A. juliana but quite common among the species of the subgenus Varria (Eales 1960), suggesting that these records are likely A. inca. Although Máncora might be the northernmost record of A. inca, it is not included here until it can be corroborated with the revision of additional material from northern Peru. Aplysia inca has been previously recorded for Pisco (Paredes et al. 1988), Ancón and Barranca (Paredes et al. 1999a), and Lobos de Tierra (Ramírez et al. 2015), although the last record needs to be verified and is not included in the distribution of the species.Published as part of Mendivil, Alejandro & Cardoso, Franz, 2022, Anatomical redescription of Aplysia (Aplysia) nigra and Aplysia (Varria) inca (Mollusca: Heterobranchia) with comments on Aplysia from Peru, pp. 201-239 in Zootaxa 5222 (3) on pages 219-232, DOI: 10.11646/zootaxa.5222.3.1, http://zenodo.org/record/746149
Métricas de autor Alejandro Gómez Jaramillo
No full textInforme de las métricas de autor del Dr. Alejandro Gómez Jaramillo de las publicaciones indexadas en Google Académico cuyo objetivo es entregar un insumo para el fortalecimiento de las capacidades y potencialidades de los autores de la Universidad Santo Tomás en el posicionamiento y visibilidad de sus publicacionesReport of the author metrics Alejandro Gómez Jaramillo of the publications indexed in Google Scholar whose objective is to provide an input for the strengthening of the capacities and potentialities of the authors of the Santo Tomás University in the positioning and visibility of their publications.http://unidadinvestigacion.usta.edu.c
Author response
No full textDetecting pathogens and mounting immune responses upon infection is crucial for animal health. However, these responses come at a high metabolic price (McKean and Lazzaro, 2011, Kominsky et al., 2010), and avoiding pathogens before infection may be advantageous. The bacterial endotoxins lipopolysaccharides (LPS) are important immune system infection cues (Abbas et al., 2014), but it remains unknown whether animals possess sensory mechanisms to detect them prior to infection. Here we show that Drosophila melanogaster display strong aversive responses to LPS and that gustatory neurons expressing Gr66a bitter receptors mediate avoidance of LPS in feeding and egg laying assays. We found the expression of the chemosensory cation channel dTRPA1 in these cells to be necessary and sufficient for LPS avoidance. Furthermore, LPS stimulates Drosophila neurons in a TRPA1-dependent manner and activates exogenous dTRPA1 channels in human cells. Our findings demonstrate that flies detect bacterial endotoxins via a gustatory pathway through TRPA1 activation as conserved molecular mechanism.sponsorship: Vlaams Instituut voor Biotechnologie Alessia Soldano Luis Franco Guangda Liu Natalia Mora Emre Yaksi Bassem A Hassanr Fonds Wetenschappelijk Onderzoek G.0702.12 Alessia Soldano Yeranddy A Alpizar Brett Boonen Alejandro Lopez-Requena Natalia Mora Thomas Voets Rudi Vennekens Bassem A Hassan Karel Talaverar Fonds Wetenschappelijk Onderzoek G.0077.15 Alessia Soldano Yeranddy A Alpizar Brett Boonen Alejandro Lopez-Requena Natalia Mora Thomas Voets Rudi Vennekens Bassem A Hassan Karel Talaverar Fonds Wetenschappelijk Onderzoek G.0680.10 Alessia Soldano Yeranddy A Alpizar Brett Boonen Alejandro Lopez-Requena Natalia Mora Thomas Voets Rudi Vennekens Bassem A Hassan Karel Talaverar Fonds Wetenschappelijk Onderzoek G.0681.10 Alessia Soldano Yeranddy A Alpizar Brett Boonen Alejandro Lopez-Requena Natalia Mora Thomas Voets Rudi Vennekens Bassem A Hassan Karel Talaverar Fonds Wetenschappelijk Onderzoek G.0503.12 Alessia Soldano Yeranddy A Alpizar Brett Boonen Alejandro Lopez-Requena Natalia Mora Thomas Voets Rudi Vennekens Bassem A Hassan Karel Talaverar Fonds Wetenschappelijk Onderzoek G.0654.15 Alessia Soldano Yeranddy A Alpizar Brett Boonen Alejandro Lopez-Requena Natalia Mora Thomas Voets Rudi Vennekens Bassem A Hassan Karel Talaverar Fonds Wetenschappelijk Onderzoek G.0761.10N Alessia Soldano Yeranddy A Alpizar Brett Boonen Alejandro Lopez-Requena Natalia Mora Thomas Voets Rudi Vennekens Bassem A Hassan Karel Talaverar Fonds Wetenschappelijk Onderzoek G.0596.12 Alessia Soldano Yeranddy A Alpizar Brett Boonen Alejandro Lopez-Requena Natalia Mora Thomas Voets Rudi Vennekens Bassem A Hassan Karel Talaverar Fonds Wetenschappelijk Onderzoek G.0565.07 Alessia Soldano Yeranddy A Alpizar Brett Boonen Alejandro Lopez-Requena Natalia Mora Thomas Voets Rudi Vennekens Bassem A Hassan Karel Talaverar KU Leuven GOA/14/011 Alessia Soldano Yeranddy A Alpizar Brett Boonen Luis Franco Alejandro Lopez-Requena Guangda Liu Natalia Mora Emre Yaksi Thomas Voets Rudi Vennekens Bassem A Hassan Karel Talaverar European Commission IUAP P7/13 Alessia Soldano Yeranddy A Alpizar Brett Boonen Luis Franco Alejandro Lopez-Requena Guangda Liu Natalia Mora Emre Yaksi Thomas Voets Rudi Vennekensr KU Leuven OT/12/091 Alessia Soldano Yeranddy A Alpizar Brett Boonen Luis Franco Alejandro Lopez-Requena Guangda Liu Natalia Mora Emre Yaksi Thomas Voets Rudi Vennekens Bassem A Hassan Karel Talaverar KU Leuven PF-TRPLe Alessia Soldano Yeranddy A Alpizar Brett Boonen Luis Franco Alejandro Lopez-Requena Guangda Liu Natalia Mora Emre Yaksi Thomas Voets Rudi Vennekens Bassem A Hassan Karel Talavera (Vlaams Instituut voor Biotechnologie, Fonds Wetenschappelijk Onderzoek|G.0702.12, Fonds Wetenschappelijk Onderzoek|G.0077.15, Fonds Wetenschappelijk Onderzoek|G.0680.10, Fonds Wetenschappelijk Onderzoek|G.0681.10, Fonds Wetenschappelijk Onderzoek|G.0503.12, Fonds Wetenschappelijk Onderzoek|G.0654.15, Fonds Wetenschappelijk Onderzoek|G.0761.10N, Fonds Wetenschappelijk Onderzoek|G.0596.12, KU Leuven|GOA/14/011, KU Leuven|OT/12/091, European Commission|IUAP P7/13, KU Leuven PF-TRPLe)status: Publishe
Alma, impulso y movimiento según Alejandro de Afrodisia
No full textthis paper discusses Alexander of Aphrodisias’ conception of the soul, paying special attention to a specific aspect distinguishing the Alexandrian view from the Aristotelian one: the impulsive capacity or faculty. Firstly, it considers Alexander’s reformulation of Aristotle’s approach to the soul (as a form of the body), a reformulation that is performed in connection with his original reconstruction of hilemorphism. At this point the author makes a special emphasis upon the manner Alexander develops a ‘terraced model’ of hilemorphic composition. Secondly, the treatment of impulsive faculty, with a special focus on the theoretical performance that Alexander derives from taking the notion of impulse, is developed. Finally, Alexander’s reformulation of the Aristotelian psychology of action is also brie y considered in order to account for the sequence of the process of the production of voluntary movement and of action. This is an explicative model that leaves aside the Aristotelian resource to the structure of the practical syllogism, and incorporates the elements predominantly characteristic of the Stoic conception. This, though, does not entail the abandonment of the basic thesis of Aristotle’s stance regarding motivation, as an opposition to socratic intellectualism: the thesis of the primacy of desire, in all its possible ways, as a factor accounting for the origin of voluntary movement and action.Este artículo se ocupa de la concepción del alma elaborada por Alejandro de Afrodisia, con especial atención a un aspecto específico que la distingue de la concepción aristotélica: la introducción de una facultad o capacidad impulsiva. En primer lugar, se considera la reformulación de la concepción jaristotélica del alma como forma del cuerpo que Alejandro lleva a cabo, en conexión con su original reconstrucción del hilemorfismo. Aquí se pone especial énfasis en el modo en el cual Alejandro construye lo que puede llamarse un “modelo escalonado” de composición hilemórfica. En segundo lugar, se considera el tratamiento de la facultad impulsiva, atendiendo especialmente al rendimiento teórico que extrae Alejandro de la adopción de la noción de impulso. Por último, se considera brevemente el modelo reformulado de psicología de la acción que elabora Alejandro, para dar cuenta de la secuencia del proceso de producción del movimiento voluntario y la acción. Se trata de un modelo explicativo que deja de lado el recurso aristotélico a la estructura del silogismo práctico e incorpora, en cambio, los elementos más característicos de la concepción estoica. Ello no implica, sin embargo, el abandono de la tesis básica de la concepción aristotélica de la motivación, por oposición al intelectualismo socrático, a saber: la tesis de la primacía del deseo, en todas sus posibles formas, como factor que da cuenta del origen del movimiento voluntario y la acción
Author-level metrics. Technical Manual. 2.0 Version
No full textBecerril-García, Arianna, Aguado-López, Eduardo, & Macedo-García, Alejandro. (2023). Author-level metrics. Technical Manual. Zenodo. https://doi.org/10.5281/zenodo.79165
"Cumbia, nena": Cumbia Scene, Gender and Class in Argentina
No full textAt the beginning of the last decade, while researching the world of Argentine soccer fans, we interviewed an important member of a fan group of the Racing de Buenos Aires soccer club. This group called itself “Los Racing Stones” and, during the interview, we discussed the reasons this name was chosen when the group formed towards the end of the 1980s. The answer, as we expected, was a play on the Rolling Stones. For a group of young white middle-class men who loved soccer almost as much as the band’s music, the name served as a way to present themselves as rockeros while also indicating-in a broad and unspecific way-that they were transgressors and “rebels.” What surprised us was what the young man said next: “But now all of that has passed. Cumbia scarfed it all down. Rock doesn’t mean anything important”(personal interview, 2001).Fil: Alabarces, Pablo Alejandro. Universidad de Buenos Aires. Facultad de Ciencias Sociales. Instituto de Investigaciones "Gino Germani"; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Silba, Malvina Leonor. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Sociales. Instituto de Investigaciones "Gino Germani"; Argentin
Cómo vamos a vivir juntos?
No full textThis book by Alejandro Aravena explores the critical question of coexistence in modern societies, particularly in the context of urban planning, social participation, and the collective challenges we face in the 21st century. The book originates from a keynote speech given by the author at the Chilean Constitutional Convention in 2021, where he reflected on the future of society and urban development over the next century.
Drawing from his extensive experience in architecture and participatory design, Aravena presents key lessons learned through real-world projects and community engagement. These principles emphasise the importance of inclusive urban planning, equitable resource distribution, and the balance between regulation and self-regulation. The book argues that solving complex social issues requires more than just good intentions. It demands a deep understanding of diverse perspectives and a willingness to embrace dialogue and collaboration.
A central theme is the idea that neither the market nor the state alone can provide sustainable solutions for urban and social challenges. Instead, the book advocates for a "third way" that trusts in people's agency, acknowledging their role as active contributors to the built environment rather than passive recipients of top-down policies. The text highlights the need to shift from mere tolerance to genuine admiration for cultural diversity, particularly in the context of the Chilean-Mapuche relationship. To this aim, the author explores the potential of indigenous knowledge, historical negotiation practices, and the power of storytelling in shaping a shared future.
By blending architectural insight with sociopolitical analysis, this book serves as a manifesto for collective responsibility, urging readers to rethink how cities, policies, and communities can be designed to foster sustainable and harmonious living conditions
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