La gran dolina

[cat] L'excavació dels nivells inferiors de la Gran Dolina (TD, 4,5,6 i 7) ha permès conèixer el moment en que va començar l’ocupació de la Sierra de Atapuerca i quins van ser els tipus d'ocupacions que s'hi van produir durant el Plistocè inferior. L’anàlisi del registre arqueo-paleontològic, que representa les estructures biòtiques i abiòtiques pretèrites, ens ha subministrat dades sobre el comportament econòmic i social dels homínids del Plistocè inferior i sobre les característiques ecològiques i climàtiques del seu entorn. La descoberta d' Homo antecessor, associat a les restes d'animals cagats i a les seves indústries Iítiques, ha ajudat a comprendre l’ocupació primigènia d'Europa per bandes d'homínids procedents d’Àfrica ara fa prop d'un milió d'anys.[eng] The excavation of the lower levels of the Gran Dolina (TD, 4,5,6 and 7) has permitted the identification of when the Sierra de Atapuerca was first settled by hominids and the types of settlements that took place during the Lower Pleistocene. The analysis of the archeo-paleontological record, which represents former biotic and abiotic structures, has provided data on the economical and social behaviour of hominids during the Lower Pleistocene and, on the ecological and climatic aspects of their environment. The discovery of Homo antecessor with associated hunted animal remains and lithic artefacts, has helped our understanding of the first settlements on Europe by hominid bands from Africa around one million years ago

Objetivación e inferencia arqueológicas como proceso lógico del conocimiento histórico.

Sin resume

Self-adaptive OmpSs tasks in heterogeneous environments

As new heterogeneous systems and hardware accelerators appear, high performance computers can reach a higher level of computational power. Nevertheless, this does not come for free: the more heterogeneity the system presents, the more complex becomes the programming task in terms of resource management. OmpSs is a task-based programming model and framework focused on the runtime exploitation of parallelism from annotated sequential applications. This paper presents a set of extensions to this framework: we show how the application programmer can expose different specialized versions of tasks (i.e. pieces of specific code targeted and optimized for a particular architecture) and how the system can choose between these versions at runtime to obtain the best performance achievable for the given application. From the results obtained in a multi-GPU system, we prove that our proposal gives flexibility to application's source code and can potentially increase application's performance.This work has been supported by the European Commission through the ENCORE project (FP7-248647), the TERAFLUX project (FP7-249013), the TEXT project (FP7-261580), the HiPEAC-3 Network of Excellence (FP7-ICT 287759), the Intel-BSC Exascale Lab collaboration project, the support of the Spanish Ministry of Education (CSD2007- 00050 and FPU program), the projects of Computación de Altas Prestaciones V and VI (TIN2007-60625, TIN2012-34557) and the Generalitat de Catalunya (2009-SGR-980).Peer ReviewedPostprint (author’s final draft

Old Info for a New Fisheries Policy: Discard Ratios and Lengths at Discarding in EU Mediterranean Bottom Trawl Fisheries

Discarding is considered globally among the most important issues for fisheries management. The recent reform of the Common Fisheries Policy establishes a landing obligation for the species which are subject to catch limits and, in the Mediterranean, for species which are subject to Minimum Conservation Reference Size (MCRS) as defined in Annex III to Regulation (EC) No 1967/2006. Additionally, several other initiatives aim to reduce unwanted catches of target and bycatch species, including species of conservation concern. This raises the need to study discarding patterns of (mainly) these species. In this work we collated a considerable amount of historical published information on discard ratios and lengths at discarding for species caught in EU Mediterranean bottom trawl fisheries. The main aim was to summarize the available historical records and make them more accessible for scientific and managerial needs, as well as to try identifying patterns in discarding. We show discard ratios and lengths at which 50% of the individuals were discarded (L50) for 15 species (9 bony fishes, three crustacean decapods, and three elasmobranchs). Discard ratios were usually low for target species such as hake, red mullets and highly commercial shrimps and exemptions from the landing obligation under the de minimis rules could be sought in several cases. Discard ratios were usually higher for commercial bycatch species. Discarding is affected by a combination of factors and for a given species, especially for non-target ones, discards are likely to fluctuate within a fishery, across seasons, years, and regions. For most species considered, L50s were lower than the MCRS (when in place) and length at first maturity. L50s of target species, such as hake, were very small due to the existence of market demands for small sized individuals. However, for species of low demand, like horse mackerels, a higher retention size was observed, often exceeding MCRS. Lengths at discarding are affected by legal provisions, market demands but also by biological, population, and ecological traits. Understanding the factors that affect discarding constitutes the starting point for designing mitigation measures and management plans to reduce discards and improve the sustainability of the stocksVersión del edito

Ribozyme-mediated compensatory induction of menin-oncosuppressor function in primary fibroblasts from MEN1 patients

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Effects of adult dysthyroidism on the morphology of hippocampal neurons.

This study investigates the effect of thyroid hormones on the morphology of hippocampal neurons in adult rats. Hypo- and hyperthyroidism were induced by adding 0.02% methimazole and 1% l-thyroxine, in drinking water from 40 days of age, respectively. When the rats were 89 days old their brains were removed and stained by a modified Golgi method and blood samples were collected in order to measure T4 serum levels. Neurons were selected and drawn using a camera lucida. Our results show that methimazole administration reduces the dendritic branching of the apical shafts of CA3 and CA1 pyramidal neurons mainly by increasing the distance to the first branch point in both types of neurons, and reducing branch points in the radius of 50 μm from the soma in CA1 neurons. Nevertheless, it was observed an increase of apical spine density in CA3 neurons from this group. Thyroxine reduces apical and basal tree of CA3 pyramidal neurons increasing the distance to the first branch point, reducing branch points in the radius of 50 μm from the soma and increases their apical and basal spine density. In CA1 field, thyroxine reduces the number of basal branch points. Both treatments seems to provoke alterations in the same direction reducing the dendritic branching and increasing spine density, although no significances appeared in some of the parameters analyzed. The effects are more evident in thyroxine than methimazole group; and in CA3 neurons than in CA1 neurons. In discussion it is pointed that the increase of spine density could be a mechanism to compensate the functionality reduction that can be provoke by the treatment effect on dendritic branching

Multiple endocrine neoplasia type 1

Multiple Endocrine Neoplasia type 1 (MEN1) is a rare autosomal dominant hereditary cancer syndrome presented mostly by tumours of the parathyroids, endocrine pancreas and anterior pituitary, and characterised by a very high penetrance and an equal sex distribution. It occurs in approximately one in 30,000 individuals. Two different forms, sporadic and familial, have been described. The sporadic form presents with two of the three principal MEN1-related endocrine tumours (parathyroid adenomas, entero-pancreatic tumours and pituitary tumours) within a single patient, while the familial form consists of a MEN1 case with at least one first degree relative showing one of the endocrine characterising tumours. Other endocrine and non-endocrine lesions, such as adrenal cortical tumours, carcinoids of the bronchi, gastrointestinal tract and thymus, lipomas, angiofibromas, collagenomas have been described. The responsible gene, MEN1, maps on chromosome 11q13 and encodes a 610 aminoacid nuclear protein, menin, with no sequence homology to other known human proteins. MEN1 syndrome is caused by inactivating mutations of the MEN1 tumour suppressor gene. This gene is probably involved in the regulation of several cell functions such as DNA replication and repair and transcriptional machinery. The combination of clinical and genetic investigations, together with the improving of molecular genetics knowledge of the syndrome, helps in the clinical management of patients. Treatment consists of surgery and/or drug therapy, often in association with radiotherapy or chemotherapy. Currently, DNA testing allows the early identification of germline mutations in asymptomatic gene carriers, to whom routine surveillance (regular biochemical and/or radiological screenings to detect the development of MEN1-associated tumours and lesions) is recommended