L'ambient urbà i la criminalitat. Robatoris contra el patrimoni a la ciutat de Girona

L’estudi de la criminalitat és multifactorial, cal destriar en la mesura del possible els factorsambientals, d’entorn urbà, que poden jugar el paper de facilitadors de la delinqüència. Lestipologies delictives són diverses i amb motivacions "mòbils" diferenciats, el que confereixdificultats a l’estudi de la criminalitat, és per aquesta raó que es trien dues tipologies derobatoris contra el patrimoni per ser analitzats: robatoris amb força a interior de domicili(vivenda) i els furts, en un marc de ciutat petita-mitjana, com és el cas de Girona. Elconeixement per part de l’autor del marc urbà n’és un part essencial per desenvolupar l’estudi.Un dels objectius finalistes és aconseguir avançar en estudis de diagnosi criminal de les ciutats;així com en el coneixement dels patrons espaials que tenen les tipologies delictives i lainfluència de les característiques del disseny urbà sobre la criminalitat. La metodologia ques’implementarà serà: recerca bibliogràfica, estadística descriptiva i inferencial, sistemesd’informació geogràfica, així com la deducció a partir de la visualització de la cartografiagenerada i un treball de camp de les zones d’alta ocurrència delictiva dels delictes esmentats.Pel que fa a les hipòtesis principals: els robatoris contra el patrimoni no es concentren en àreesdegradades urbanísticament sinó ans el contrari en ambients urbans cuidats. Aquesta hipòtesies contraposa a la teoria criminal de la "Broken Windows", que esmenta que els espais urbansdegradats és on hi ha menys ocupació d’espai públic i més delinqüència. Una altra hipòtesiimportant és que els espais percebuts com a segurs, respecte les tipologies delictivesesmentades, són els més insegurs

Experimental investigation of transient natural convection cooling of high prandtl number fluid with variable viscosity

Report for the scientific sojourn at the James Cook University, Australia, between June to December 2007. Free convection in enclosed spaces is found widely in natural and industrial systems. It is a topic of primary interest because in many systems it provides the largest resistance to the heat transfer in comparison with other heat transfer modes. In such systems the convection is driven by a density gradient within the fluid, which, usually, is produced by a temperature difference between the fluid and surrounding walls. In the oil industry, the oil, which has High Prandtl, usually is stored and transported in large tanks at temperatures high enough to keep its viscosity and, thus the pumping requirements, to a reasonable level. A temperature difference between the fluid and the walls of the container may give rise to the unsteady buoyancy force and hence the unsteady natural convection. In the initial period of cooling the natural convection regime dominates over the conduction contribution. As the oil cools down it typically becomes more viscous and this increase of viscosity inhibits the convection. At this point the oil viscosity becomes very large and unloading of the tank becomes very difficult. For this reason it is of primary interest to be able to predict the cooling rate of the oil. The general objective of this work is to develop and validate a simulation tool able to predict the cooling rates of high Prandtl fluid considering the variable viscosity effects.

Little evidence for association between the TGFBR1*6A variant and colorectal cancer: a family-based association study on non-syndromic family members from Australia and Spain.

Genome-wide linkage studies have identified the 9q22 chromosomal region as linked with colorectal cancer (CRC) predisposition. A candidate gene in this region is transforming growth factor beta receptor 1 (TGFBR1). Investigation of TGFBR1 has focused on the common genetic variant rs11466445, a short exonic deletion of nine base pairs which results in truncation of a stretch of nine alanine residues to six alanine residues in the gene product. While the six alanine (*6A) allele has been reported to be associated with increased risk of CRC in some population based study groups this association remains the subject of robust debate. To date, reports have been limited to population-based case-control association studies, or case-control studies of CRC families selecting one affected individual per family. No study has yet taken advantage of all the genetic information provided by multiplex CRC families. Methods: We have tested for an association between rs11466445 and risk of CRC using several family-based statistical tests in a new study group comprising members of non-syndromic high risk CRC families sourced from three familial cancer centres, two in Australia and one in Spain. Results: We report a finding of a nominally significant result using the pedigree-based association test approach (PBAT; p = 0.028), while other family-based tests were non-significant, but with a p-value < 0.10 in each instance. These other tests included the Generalised Disequilibrium Test (GDT; p = 0.085), parent of origin GDT Generalised Disequilibrium Test (GDT-PO; p = 0.081) and empirical Family-Based Association Test (FBAT; p = 0.096, additive model). Related-person case-control testing using the 'More Powerful' Quasi-Likelihood Score Test did not provide any evidence for association (M-QL5; p = 0.41). Conclusions: After conservatively taking into account considerations for multiple hypothesis testing, we find little evidence for an association between the TGFBR1*6A allele and CRC risk in these families. The weak support for an increase in risk in CRC predisposed families is in agreement with recent meta-analyses of case-control studies, which estimate only a modest increase in sporadic CRC risk among 6*A allele carriers.