Caracterización y clasificación de la red hidrográfica de la cuenca del río Bobo, departamento de Nariño - Colombia

The object of this work was to make a morphometric characterization of the Bobo river watershed in the Nariño department in Colombia. A map was created from topographical maps (1:25.000 scale) using the drainage network and the limit of each 2nd order microbasin as database. Dimensional, drainage network and relief morphometric parameters were evaluated for a later hy-drological study. The drainage area was 224.97 km2, having a 71.31 km perimeter. The Bobo river watershed is considered to be 6th order and has 176 2nd order drainage channels, 34 3rd order drainage channels, 9 4th order drainage channels and 3 5th order drainage channels. Average drainage density is 3.71km/km2, reflecting its high density, having strong, dissected geological formation. The area has a typical Andean land-use pattern, having native wooded vegetation, traditional transitory potato and vegetable growing predominating.

Gestión del agua a nivel de cuencas: teoría y práctica

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Informe de la Reunión Regional de América Latina y el Caribe Preparatoria del Año Internacional de la Familia = Report of the Latin American and Caribbean Regional Meeting Preparatory to the International Year of the Family

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On the existence of G-equivariant maps

Let G be a compact Lie group. Let X, Y be free G-spaces. In this paper, by using the numerical index i (X; R), under cohomological conditions on the spaces X and Y, we consider the question of the existence of G-equivariant maps f: X -> Y.

El Antropoceno: haciendo y difundiendo ciencia

[ES] En esta charla el ponente cuenta cómo ha participado en la organización de una campaña a favor de la introducción de una nueva era geológica, el Antropoceno. En particular, repasa las dos contribuciones a las sesiones científicas preparatorias, y da su opinión particular sobre ello.

¿Presenta la anémona Anemonia sulcata (Pennant, 1777) comportamiento de homing?

[ES] Se estudia la capacidad de retorno al lugar de origen en Anemonia sulcata en su medio natural. Treinta y dos individuos fueron marcados en charcas intermareales, de los cuales 20 fueron desplazados, 5 y 10cm, de sus posiciones originales. Posteriormente se observó el movimiento de todos ellos en las siguientes 48h. De todas las anémonas trasladadas, un único individuo volvió exactamente a su lugar de origen recorriendo, en las primeras 24h, los 10cm que había sido desplazado. Con los resultados obtenidos en este trabajo, Anemonia sulcata no parece presentar fidelidad por un lugar en concreto dentro de su charca. Al ser trasladado desde su lugar inicial, simplemente busca un nuevo punto de fijación y lo hace tomando una dirección aleatoria. A falta de estudios más exhaustivos, se puede afirmar que esta especie no presenta comportamiento de homing.

The mutation causing the black-and-tan pigmentation phenotype of Mangalitza pigs maps to the porcine ASIP locus but does not affect its coding sequence

The gene for agouti signaling protein (ASIP) is centrally involved in the expression of coat color traits in animals. The Mangalitza pig breed is characterized by a black-and-tan phenotype with black dorsal pigmentation and yellow or white ventral pigmentation. We investigated a Mangalitza x Piétrain cross and observed a coat color segregation pattern in the F2 generation that can be explained by virtue of two alleles at the MC1R locus and two alleles at the ASIP locus. Complete linkage of the black-and-tan phenotype to microsatellite alleles at the ASIP locus on SSC 17q21 was observed. Corroborated by the knowledge of similar mouse coat color mutants, it seems therefore conceivable that the black-and-tan pigmentation of Mangalitza pigs is caused by an ASIP allele a(t), which is recessive to the wild-type allele A. Toward positional cloning of the a(t) mutation, a 200-kb genomic BAC/PAC contig of this chromosomal region has been constructed and subsequently sequenced. Full-length ASIP cDNAs obtained by RACE differed in their 5' untranslated regions, whereas they shared a common open reading frame. Comparative sequencing of all ASIP exons and ASIP cDNAs between Mangalitza and Piétrain pigs did not reveal any differences associated with the coat color phenotype. Relative qRT-PCR analyses showed different dorsoventral skin expression intensities of the five ASIP transcripts in black-and-tan Mangalitza. The a(t) mutation is therefore probably a regulatory ASIP mutation that alters its dorsoventral expression pattern.

The bovine dilated cardiomyopathy locus maps to a 1.0-Mb interval on chromosome 18

Cardiomyopathies are myocardial diseases that lead to cardiac dysfunction, heart failure, arrhythmia, and sudden death. In human medicine, cardiomyopathies frequently warrant heart transplantation in children and adults. Bovine dilated cardiomyopathy (BDCMP) is a heart muscle disorder that has been observed during the last 30 years in cattle of Holstein-Friesian origin. In Switzerland BDCMP affects Swiss Fleckvieh and Red Holstein breeds. BDCMP is characterized by a cardiac enlargement with ventricular remodeling and chamber dilatation. The common symptoms in affected animals are subacute subcutaneous edema, congestion of the jugular veins, and tachycardia with gallop rhythm. A cardiomegaly with dilatation and hypertrophy of all heart chambers, myocardial degeneration, and fibrosis are typical postmortem findings. It was shown that all BDCMP cases reported worldwide traced back to a red factor-carrying Holstein-Friesian bull, ABC Reflection Sovereign. An autosomal recessive mode of inheritance was proposed for BDCMP. Recently, the disease locus was mapped to a 6.7-Mb interval MSBDCMP06-BMS2785 on bovine Chr 18 (BTA18). In the present study the BDCMP locus was fine mapped by using a combined strategy of homozygosity mapping and association study. A BAC contig of 2.9 Mb encompassing the crucial interval was constructed to establish the correct marker order on BTA18. We show that the disease locus is located in a gene-rich interval of 1.0 Mb and is flanked by the microsatellite markers DIK3006 and MSBDCMP51.

Arachnomelia in Brown Swiss cattle maps to chromosome 5

Arachnomelia in Brown Swiss cattle is a monogenic autosomal recessive inherited congenital disorder of the skeletal system giving affected calves a spidery look (OMIA ID 000059). Over a period of 20 years 15 cases were sampled in the Swiss and Italian Brown cattle population. Pedigree data revealed that all affected individuals trace back to a single acknowledged carrier founder sire. A genome scan using 240 microsatellites spanning the 29 bovine autosomes showed homozygosity at three adjacent microsatellite markers on bovine Chr 5 in all cases. Linkage analysis confirmed the localization of the arachnomelia mutation in the region of the marker ETH10. Fine-mapping and haplotype analysis using a total of 34 markers in this region refined the critical region of the arachnomelia locus to a 7.19-Mb interval on bovine Chr 5. The disease-associated IBD haplotype was shared by 36 proven carrier animals and allows marker-assisted selection. As the corresponding human and mouse chromosome segments do not contain any clear functional candidate genes for this disorder, the mutation causing arachnomelia in the Brown Swiss cattle might help to identify an unknown gene in bone development.