198,740 research outputs found
Data for: The DNAJ gene family in yerba mate (Ilex paraguariensis): genome-wide identification, structural characterization, orthology based classification and expression analysis
No full textThis publication holds the entire supplementary material to the contribution in Rodriguésia "The DNAJ gene family in yerba mate (Ilex paraguariensis): genome-wide identification, structural characterization, orthology based classification and expression analysis" by Aguilera et al
Phenological Stages and Aluminum Presence Influences Arbuscular Mycorrhizal Fungi Communities in Roots of Plant Cereals
No full textThis study was financially supported by FONDECYT 11170641 (P. Aguilera), from Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT-ANID Chile), MEC 80190060 (P. Aguilera), and Campex Semillas Baer
[Costumbres y ceremonias de la Congregación de San Benito de Valladolid] [Manuscrito]
No full text[17] f., 98 p., [18] f. ; 14 cmSignatura: Ms 570Castelán. Na f. 1 conserva un fragmento dun " Soneto a la ambre de los Novicios". Na f. 3 nota, probablemente do P. Luis Manuel de Aguilera, posuidor e probable copistaPaxinación antiga a tinta. Deterioradas as follas ó principio e ó final. Incompleto ó finalEnc. en pergame
Miohepatus Lima & Silva & Aguilera & Pinheiro & Santana 2023, new genus
No full textGenus <i>Miohepatus</i> new genus https://zoobank.org/ 76AE969B-27E0-4112-85A5-DDE9B2F5A503 <p> <b>Type species:</b> <i>Hepatella amazonica</i> Beurlen, 1958, by present designation. Gender masculine.</p>Published as part of <i>Lima, Daniel, Silva, Rafael Costa da, Aguilera, Orangel, Pinheiro, Allysson Pontes & Santana, William, 2023, Brazilian Miocene crabs I. Taxonomic review of Cyclocancer tuberculatus Beurlen, 1958 and Hepatella amazonica Beurlen, 1958 (Pancrustacea, Decapoda, Brachyura), pp. 1-9 in Papéis Avulsos de Zoologia 63</i> on page
Reseña de Cuadros Aguilera, P., La donación de sangre. Historia y crítica de su regulación, Civitas, Pamplona, 2018
No full textObra ressenyada: Pol CUADROS AGUILERA, La donación de sangre. Historia y crítica de su regulación. Pamplona: Editorial Civitas, 201
A Proof of Grilliot's Theorem
No full textWe would like to thank Juliette Kennedy, Phokion Kolaitis, and Andreas Weiermann for their comments. The first author was partially supported by FWF grant I4513N and FWO grant 3E017319. The second author was partially supported by FWO grant 11O0923N
Psychological characteristics of the battering man of his permanent partner, residing in the city of Bucaramanga
No full textEvaluar las características de personalidad de los hombres golpeadores de la compañera permanente. Método: 50 agresores registrados en la Fiscalía General de la Nación se evaluaron por medio de las pruebas BFQ y IMAFE, y por entrevista cualitativa estructurada. Resultados: Los hombres agresores puntuaron “muy bajo” en cultura, información, cooperativismo, cordialidad, altruismo, amistad, generosidad y empatía; “bajo” en reflexión, escrupulosidad, orden, diligencia, perseverancia, dinamismo y energía; y “muy alto” en sumisión, ser taciturno, ansiedad, vulnerabilidad, emotividad, impulsividad, impaciencia e irritabilidad. La mayoría identifican los rasgos de pasividad, timidez, inseguridad, emotividad, sumisión como culturalmente asociados al ser femenino. En la entrevista cualitativa se estableció que atribuyen como causas de su comportamiento a circunstancias externas y ajenas a voluntad, como la situación económica, el abuso del alcohol o el comportamiento de la compañera; consideran sus actos violentos como producto del entorno socio-cultural y de las circunstancias ambientales, no identificándose como responsables de la agresión contra su compañera. Conclusión: El hombre agresor de la compa-ñera permanente es conservador, apegado a los valores patriarcales y resistente al cambio, lo que se reflejan en sus características de personalidad y en los sentidos y significados que le atribuye al comportamiento violento. Probablemente esto puede reflejar sentimientos homofóbicos y misogínicos producto de crisis de identidad de género y del proceso de construcción de la masculinidad, en la medida en que no responden a las exigencias que la cultura patriarcal le plan-tea al “macho”. [Aguilera A. Características psicológicas del hombre golpeador de su compañera permanente. MedUNAB 2004; 7:73-83]Evaluate the personality characteristics of the male batterers of the permanent partner. Method: 50 offenders registered with the Attorney General's Office were evaluated through the BFQ and IMAFE tests, and by structured qualitative interview. Results: The male aggressors scored "very low" in culture, information, cooperativism, cordiality, altruism, friendship, generosity and empathy; “Low” in reflection, conscientiousness, order, diligence, perseverance, dynamism and energy; and "very high" in submission, being taciturn, anxious, vulnerable, emotional, impulsive, impatient, and irritable. Most identify the traits of passivity, shyness, insecurity, emotionality, submission as culturally associated with being female. In the qualitative interview, it was established that they attribute as causes of their behavior to external circumstances beyond their control, such as the economic situation, alcohol abuse or the behavior of the partner; They consider their violent acts as a product of the socio-cultural environment and environmental circumstances, not identifying themselves as responsible for the aggression against their partner. Conclusion: The male aggressor of the permanent partner is conservative, attached to patriarchal values and resistant to change, which is reflected in his personality characteristics and in the meanings and meanings that he attributes to violent behavior. This may probably reflect homophobic and misogynic feelings as a result of the crisis of gender identity and the process of construction of masculinity, insofar as they do not respond to the demands that the patriarchal culture places on the “male”. [Aguilera A. Psychological characteristics of the battering man of his permanent partner. MedUNAB 2004; 7: 73-83
Jenynsia tucumana Aguilera & Mirande, 2005, new species
No full text<p>Jenynsia tucumana, new species</p> <p>(Fig. 2)</p> <p>Holotype. CI-FML 3828, Male, 30.7 mm SL, Argentina, Tucumán, Dpto. Trancas, río Vípos (26°28’S; 65°20’W), 5 km from Ruta Nacional 9, G. Aguilera and M. Mirande, April 24, 2003.</p> <p>Paratypes. CI-FML 3829, 4, 26.2-32.8 mm SL; AI 163, 6, 26.3-40.4 mm SL; ANSP 180781, 6, 20.4-33.0 mm SL; CI-FML 3840, 2 C&S, 28.3-36.0, collected with holotype.</p> <p>Diagnosis. Jenynsia tucumana n. sp. is distinguished from other members of the genus by the possession of a row of dark markings ranging from dots to small vertical stripes, on the lateral surface, from the tip of the adpressed pectoral fin to the margin of hypural (Fig.2).</p> <p>Among the remaining species of the genus only Jenynsia alternimaculata has vertical stripes, but its pattern is different from that of the new species (two occasionally three rows of dorsoventrally elongate markings on the lateral surface of body vs. one row of short vertical stripes or dots in the new species). These differences are further elaborated below under “ Results and Discussion”. Jenynsia tucumana may also be distinguished from J. alternimaculata by the possession of a mandibular canal pore W, a wide prootic bridge, and a symmetric fifth anal-fin ray of the tubular gonopodium; from J. pygogramma by the number of predorsal scales (15-16 vs. 19-25); from J. multidentata, J. maculata and J. lineata (Jenyns) by the absence of a swelling between the urogenital opening and the anterior base of the anal fin in females; from J. sanctaecatarinae by the absence of a rounded spot on dorsal pectoral-fin base; and from J. onca by the absence of a large dorsal convex expansion at subdistal segments of right half of sixth anal-fin ray of adult males. Jenynsia tucumana can be distinguished from J. eirmostigma Ghedotti and Weitzman, J. weitzmani, J. eigenmanni, and J. unitaenia Ghedotti and Weitzman by the absence of a long posterodorsal process of the lachrymal and a shorter fourth anal-fin ray in the gonopodium.</p> <p>Description. Body elongate, slightly compressed laterally; greatest body depth at vertical between pectoral and pelvic fins; mouth terminal, slightly oblique; tricuspid teeth in premaxilla and dentary. Dorsal-fin origin at vertical through or just behind first anal-fin ray insertion. Sexual dimorphism present, males much smaller than females, with tubular intromittent organ formed by 8 first anal-fin rays; length of gonopodium 1.3-1.5 in caudal peduncle; posterior two anal-fin rays not forming part of tubular intromittent organ and extending approximately two-thirds of gonopodium length. Females without swelling between urogenital opening and anterior base of anal fin. Head squamation pattern as in figure 3; anterior branch of supra-orbital sensory canal formed by pores 1 and 2a; middle part by 2b, 3, 4a, and posterior branch by 4b, 5, 6, 7; preopercular canal continuous, with 7 pores; infraorbital canal formed by 4 pores; mandibular canal with pores X, Ya, Yb, Z and W.</p> <p>Morphometric measurements expressed as percents of standard length in table 1. Counts of 47 specimens, including the holotype: lateral scale series 31[11], 32[17], 33*[15], 34[4]; predorsal scales 14[5], 15[20], 16*[21]; circumpeduncular scales 16*[47]; dorsal-fin rays 7*[11], 8[36]; anal-fin rays in females 10[19], 11[1]; pectoral-fin rays 15[8], 16[26], 17*[13]; pelvic-fin rays 6*[47]; caudal-fin rays 16[10], 17[15], 18*[22]. Counts in C&S specimens: gill rakers 10[5], 11[4], 12[1]; vertebrae 31[3], 32[5]; gonopodium 10[5].</p> <p>Coloration in alcohol: Body background color grading from brown dorsally to cream ventrally. Dark chromatophores in center of scales, present on dorsal part of body to fifth row of scales. Mid-dorsal stripe of dark chromatophores from posterior part of head to first dorsal-fin ray insertion; base of dorsal fin light brown; mid-dorsal stripe continued on upper portion of peduncle to anterior procurrent caudal-fin rays. Concentration of chromatophores present on two scales anterior to dorsal-fin origin. Mid-lateral row of dark markings ranging from dots to small vertical stripes, from adpressed tip of pectoral fin to posterior margin of hypural. Anterior part of this row with dark dashes irregularly distributed. Two rows of rounded dark dashes posteriorly directed in dorsal view, from vertical through pectoral-fin insertion, turning to dorso-lateral at vertical through pelvicfin insertion, and reaching 4/5 of peduncle length. Some specimens with third row of dark dashes under mid-lateral row, reaching 4/5 of peduncle length. Isthmus unpigmented. All fins with scattered chromatophores in membranes, surrounding some rays. Diffuse subdermal stripe ventrally, from posterior anal-fin insertion to half caudal peduncle length. Dark chromatophores scattered over entire surface of gonopodium.</p> <p>Head brown dorsally, cream ventrally; a dark brown blotch on postero-dorsal surface of the head, extending anteriorly between the eyes. Dark brown dashes between anterior branch of supra-orbital sensory canal and posterior nares. Dark chromatophores scattered over premaxilla, lower jaw and pre-orbital canal area. Upper part of opercle with a horizontal strip. Branchiostegal membranes unpigmented.</p> <p>Distribution. Jenynsia tucumana n. sp. is known from Río Vípos, Río Calera, and Río Grande; all of which are in the upper Río Salí basin (Fig. 4).</p> <p>Etymology. The specific epithet tucumana means “from Tucumân ” province in Argentina, where the type locality is situated.</p> <p>Remarks. This species mainly inhabits moderate to slow flowing streams with rocky bottom and algae on the substrate, where it is sympatric with Jenynsia multidentata.</p> <p>Results and Discussion. Jenynsia tucumana shares two uniquely derived characters with the members of the subgenus Jenynsia (Ghedotti 1998): the lack of segmentation on the proximal and distal quarters of sixth anal-fin ray in adult males and the vertically inclined proximal radials associated with the first six anal-fin rays in the gonopodium.</p> <p>The unique coloration pattern distinguishes the new species from the remaining species of the genus. Although the pattern in J. tucumana resembles that of Jenynsia alternimaculata (i.e. vertical stripes on lateral surface of body), the former species has only one row of markings vs. two or three in the latter (see Fig. 4 in Ghedotti & Weitzman, 1996). In addition J. alternimaculata has the left and right halves of anal-fin ray five asymmetric; this apomorphy, shared with J. sanctaecatarinae, is absent in J. tucumana in which both halves are similar in size. Jenynsia alternimaculata also has, as an autoapomorphic condition, a narrow prootic bridge, which is an additional character to distinguish this species from J. tucumana and from the remaining species of the genus.</p> <p>A single, most parsimonious tree of 147 steps was obtained with concavity constants (K) ranging from 0.0001 to 6 (Fig. 5b), and in concavities from 7 to 100, the most parsimonious tree, with 146 steps, is one of the four most parsimonious trees under equal weights (Fig. 5a,c). Low concavity constants and equal weighting (or high concavity constants) represent opposite extreme cases in which the homoplastic characters are almost ignored, or are considered as reliable as the perfectly hierarchic ones respectively. Since the results produced by either extreme are very similar, those results clearly do not depend entirely on decisions of whether (or how strongly) to weight characters.</p> <p>Regardless of weighting strength, Jenynsia tucumana belongs to the subgenus Jenynsia. The relationships of the new species vary slightly between the analyses performed due to differing relationships of J. sanctaecatarinae, as in the analysis of Lucinda et al. (2002). The latter species is the sister group of J. alternimaculata under concavities 0.0001 to 6, and the sister group of J. onca under concavities 7 to 100; under equal weights, J. sanctaecatarinae collapses basally to J. tucumana. Thus, position of the new species is basal to the remaining species of the subgenus Jenynsia, except J. onca and, for concavities below 7, also J. sanctaecatarinae.</p> <p>Five species of Jenynsia are present in Argentina: the widely distributed J. multidentata and the exclusively northwesterly distributed J. alternimaculata, J. maculata, J. pygogramma and J. tucumana. Jenynsia multidentata was considered to occur in lowlands (Ghedotti & Weitzman, 1996 and Ghedotti, 1998), but we have found it together with J. tucumana in highland streams at 1200 meters above sea level. The distribution of the genus in northwestern Argentina coincides with the proposed extension of the Paranean Sea, in the Middle-Upper Miocene (Aceñolaza & Sprechmann, 2002); this sea would have extended westward on the Brazilian/Uruguayan platform, flooding a big area of central-northern Argentina and central Paraguay, and may have acted as a barrier between southeastern Brazilian-Uruguayan and northwestern Argentine populations/ species (compare fig. 1 of Aceñolaza & Sprechmann, 2002 with fig. 29 of Ghedotti, 1998). Also, the northwestern Argentina species (or its ancestor/ancestors) probably was/were coastal species before the recession of the Paranean Sea and now are restricted to highlands. Nevertheless, this is only a hypothesis that could be corroborated or refuted only with additional information on the systematics and evolutionary history of the genus.</p>Published as part of <i>Gastón Aguilera & Juan Marcos Mirande, 2005, A new species of Jenynsia (Cyprinodontiformes: Anablepidae) from northwestern Argentina and its phylogenetic relationships., pp. 29-39 in Zootaxa 1096</i> on pages 33-3
Sciades maldonadonis Carrillo-Briceño & Mora-Rojas & Hendricks & Vanegas & Aguilera 2023, n. sp.
No full text† <i>Sciades maldonadonis</i> n. sp. <p>(Fig. 3 A1-A3)</p> <p>urn:lsid:zoobank.org:act: A20896FF-45B6-4E90-9A8C-22E9A791748E</p> <p> DIAGNOSIS. — The combination of extremely depressed lapillus otolith, regularly clam-shaped outline, sharp antero-medial projection, strongly arched dorsal margin anteriorly and oblique-straight posteriorly distinguish † <i>Sciades maldonadonis</i> n. sp. from extant <i>Sciades</i> species, extinct brackish and freshwater species (e.g., † <i>Cantarius</i> Aguilera <i>et al.</i>, 2013b), and extant South American freshwater species (<i>Chinchaysuyoa</i> Marceniuk <i>et al.</i>, 2019a, and <i>Paragenidens</i> Marceniuk <i>et al.</i>, 2019a).</p> <p>TYPE MATERIAL. — Holotype VPPLT-832. A complete lapillus otolith (Fig. 3 A1-A3), preserved length 20.94 mm, width 16.84 mm, thickness 7.08 mm.</p> <p> TYPE LOCALITY. — <b>La Victoria Fm</b>. Morrongo 1 (see Fig. 1 B; Appendix 1).</p> <p> DERIVATION OF NAME. <b>—</b> The species is named in honor of Dr Javier Alejandro Maldonado-Ocampo (1977-†2019), renowned Colombian ichthyologist who passed away on 2 March 2019 during an expedition to the Río Vaupés in Colombia. Javier dedicated more than twenty years to the study and conservation of the freshwater fish fauna of Colombia, including the Andes, Orinoco and Amazon basins.</p> <p>DESCRIPTION</p> <p>The lapillus otolith is clam-shaped with a semi-circular outline, very depressed dorso-ventrally, and with a sharp antero-medial projection (Fig. 3 A1, A2). The dorsal margin is strongly arched anteriorly and oblique-straight posteriorly. The ventral margin is strongly arched. The posterior margin forms an obtuse angle. The lateral profile is slightly biconvex. The pseudocauda and the mesial inward curvature are not well preserved. The umbo is located in the center of the dorsal surface. The lapillus length to width ratio: 1.2. Lapillus length to thickness ratio: 3.0.</p> <p>REMARKS</p> <p> VPPLT-832 is characterized by a typical Ariidae otolith morphology. The recognition of † <i>Sciades maldonadonis</i> n. sp. as a member of <i>Sciades</i> is based on its otolith morphology, which is characterized by the combination of extremely depressed dorsoventral shape and by the dorsal margin being strongly arched anteriorly, and oblique-straight posteriorly. This allows it to be differentiated from the other <i>Sciades</i> species (for comparative proposes see Aguilera <i>et al.</i> 2020: figs. 4.49-4.60; 6.9-6.12).</p> <p> Marceniuk <i>et al.</i> (2017) reviewed the genus <i>Sciades</i> and showed a strong morphological relationship between nominal genera <i>Sciades</i> and <i>Ariopsis</i> Gill, 1861. More than seven extant <i>Sciades</i> species are currently recognized (Froese & Pauly 2022). The age of diversification of modern species of <i>Sciades</i> is older than 9 Ma (including <i>Sciades dowii</i> Gill, 1863, from the Pacific), and the age of the Atlantic <i>Sciades</i> species is <i>c.</i> 6.7 Ma (4-8Ma) (Betancur-R.2009). † <i>Sciades maldonadonis</i> n. sp. came from a freshwater palaeoenvironment in the middle Miocene rocks of the Honda Group, associated with a wide diversity of freshwater fishes, crocodylians, snakes, lizards, turtles, and mammals (e.g., Kay <i>et al.</i> 1997; Carrillo <i>et al.</i> 2015; Cadena <i>et al.</i> 2019, 2020; Defler 2019). The ancestral form of freshwater catfish Ariidae otolith-based species from the western Amazon included † <i>Cantarius nolfi</i> Aguilera, Moraes-Santos, Costa, Ohe, Jaramillo & Nogueira, 2013b, and † <i>Cantarius ohei</i> Schwarzhans, Aguilera, Scheyer & Carrillo-Briceño, 2022, recorded from the Miocene Pebas wetland system at the Pebas Formation (Carrillo-Briceño <i>et al.</i> 2021b; Schwarzhans <i>et al.</i> 2022). In North, Central, and South America, six extant ariid species are primarily freshwater, including <i>Chinchaysuyoa labiata</i> Boulenger, 1898, <i>Chinchaysuyoa ortegai</i> Marceniuk, Marchena, Oliveira & Betancur-R, 2019a, <i>Paragenidens grandoculis</i> Steindachner, 1877, <i>Paragenidens nelsoni</i> Evermann & Goldsborough, 1902, <i>Paragenidens izabalensis</i> Hubbs & Miller, 1960, and <i>Paragenidens usumacintae</i> Betancur-R & Willink, 2007 (Marceniuk & Menezes 2007; Marceniuk <i>et al.</i> 2019a, b). On the other hand, fossil skull-based species of † <i>Sciades latissimum</i> Aguilera & Marceniuk, 2018, and † <i>Sciades peregrinus</i> Aguilera & Marceniuk, 2018 without preserved internal otolith, were described from the late Miocene Urumaco Fm, Venezuela, characterized by palaeoenvironments associated to a large palaeo-hydrographic system of the Orinoco/ Amazonas discharging into the proto-Caribbean Sea (Aguilera <i>et al.</i> 2020).</p> <p>Other ariid remains from the Honda Group include two isolated dorsal-spine fragments ornamented by rugose tuberculations, from the Duke 24 (see Lundberg 1997) and Mini Desierto localities (VPPLT-1108; Figs 1 B, 3 B1-B3). Sedimentary characteristics and the associated fauna from the Honda Group support that VPPLT-832 and the indeterminate ariid spines were from a freshwater palaeoenvironment.</p>Published as part of <i>Carrillo-Briceño, Jorge D., Mora-Rojas, Laura, Hendricks, Kimberly, Vanegas, Andrés & Aguilera, Orangel, 2023, New clues on the palaeodiversity of the middle Miocene freshwater ichthyofauna from the Tatacoa Desert, Colombia, pp. 327-351 in Geodiversitas 45 (10)</i> on page 335, DOI: 10.5252/geodiversitas2023v45a10, <a href="http://zenodo.org/record/8056044">http://zenodo.org/record/8056044</a>
Author-wise bibliometric analysis based on entropy.
No full textAuthor-wise bibliometric analysis based on entropy.</p
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