Numerical modelling of a turbulent bluff-body flow with Reynolds stress turbulent models

Numerical modelling of a turbulent bluff-body flow has been performed using differential Reynolds stress models (DRSMs). To clarify the applicability of the existing DRSMs in this complex flow, several typical DRSMs, including LRR-IP model, JM model, SSG model, as well as a modified LRR-IP model, have been validated and evaluated. The performance difference between various DRSMs is quite significant. Most of the above mentioned DRSMs cannot provide overall satisfactory predictions for this challenging test case. Motivated by the deficiency of the existing approaches, a new modification of LRR-IP model has been proposed. A very significant improvement of the prediction of flow field is obtained.     

Plausibility in Early Stages of Architectural Design: A New Tool for High-Rise Residential Buildings

This paper analyzes the problem of the design of envelopes for high-rise isolated residential buildings. The phenomenon of envelope creation appears in the early stages of the architectural design. Variables that influence the final shape and size of such envelopes are then identified. This paper presents the state-of-the-art tools for the current solutions at the commercial and academic/scientific level. The variables identified in this research are the client’s needs, the urban code and architectural prac...     

Spatial organization of northern flying squirrels, Glaucomys sabrinus: territoriality in females?

We determined home-range overlap among northern flying squirrels ( Glaucomys sabrinus ) to assess their spatial organization. We found extensive home-range overlap among females, and though this overlap could reflect social behavior, we found no evidence of attraction among females, with only one instance of den-sharing. Instead, our results suggest that females share foraging areas but may be territorial in portions of the home range, especially around den trees and during young-rearing. Home-range overlap could also result from the extrinsic effect of forest fragmentation due to timber harvest, which might impede dispersal and force squirrels to cluster on remaining fragments of suitable habitat. Determinamos el sobrelapamiento del rango hogareño entre las ardillas voladoras del norte ( Glaucomys sabrinus ) para evaluar su organización espacial. Encontramos un extenso sobrelapamientos en los rangos hogareños entre las hembras; aunque esto podría reflejar su comportamiento social, no encontramos evidencia de atracción entre hembras, y en sólo un caso compartieron su guarida. Vienen su lugar, nuestros resultados sugieren que las hembras comparten áreas de forrajeo pero pueden ser territoriales en ciertas partes de su rango hogareño, particularmente cerca de los árboles donde tienen guaridas y cuando tienen cría. El sobrelapamiento del rango hogareño también podría ser el resultado del efecto extrínseco de la fragmentación forestal debido a la tala de madera, el cual podría impedir la dispersión y forzar a las ardillas a agruparse en fragmentos de hábitat adecuado que queden.     

Serologic survey of the island spotted skunk on Santa Cruz Island

Two rare endemic carnivores occur on California's northern Channel Islands: island spotted skunks ( Spilogale gracilis amphiala ) and island foxes ( Urocyon littoralis ). As insular carnivores, both may be particularly vulnerable to novel pathogens. We tested sera from 31 island spotted skunks on Santa Cruz Island, where both skunks and foxes occur sympatrically, to establish their exposure to disease agents. One skunk (3%) tested positive for canine heartworm, and 3 skunks (10%) tested positive for canine parvovirus. None showed evidence of exposure to canine adenovirus, canine distemper virus, canine herpesvirus, Leptospira bacteria (serovars pomona , canicola , and icterohaemorrhagiae ), or pseudorabies virus. Spotted skunks on Santa Cruz Island apparently have low susceptibility or exposure to these pathogens and are unlikely to be reservoirs of these diseases for island foxes.     

Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness

Using exome sequencing, we identify SERAC1 mutations as the cause of MEGDEL syndrome, a recessive disorder of dystonia and deafness with Leigh-like syndrome, impaired oxidative phosphorylation and 3-methylglutaconic aciduria. We localized SERAC1 at the interface between the mitochondria and the endoplasmic reticulum in the mitochondria-associated membrane fraction that is essential for phospholipid exchange. A phospholipid analysis in patient fibroblasts showed elevated concentrations of phosphatidylglycerol-34:1 (where the species nomenclature denotes the number of carbon atoms in the two acyl chains:number of double bonds in the two acyl groups) and decreased concentrations of phosphatidylglycerol-36:1 species, resulting in an altered cardiolipin subspecies composition. We also detected low concentrations of bis(monoacyl-glycerol)-phosphate, leading to the accumulation of free cholesterol, as shown by abnormal filipin staining. Complementation of patient fibroblasts with wild-type human SERAC1 by lentiviral infection led to a decrease and partial normalization of the mean ratio of phosphatidylglycerol-34:1 to phosphatidylglycerol-36:1. Our data identify SERAC1 as a key player in the phosphatidylglycerol remodeling that is essential for both mitochondrial function and intracellular cholesterol trafficking.     

Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification

Idiopathic infantile arterial calcification (IIAC; OMIM 208000) is characterized by calcification of the internal elastic lamina of muscular arteries and stenosis due to myointimal proliferation. We analyzed affected individuals from 11 unrelated kindreds and found that IIAC was associated with mutations that inactivated ecto-nucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1). This cell surface enzyme generates inorganic pyrophosphate (PP(i)), a solute that regulates cell differentiation and serves as an essential physiologic inhibitor of calcification.     

Identification of genetic elements that autonomously determine DNA methylation states

Cytosine methylation is a repressive, epigenetically propagated DNA modification. Although patterns of DNA methylation seem tightly regulated in mammals, it is unclear how these are specified and to what extent this process entails genetic or epigenetic regulation. To dissect the role of the underlying DNA sequence, we sequentially inserted over 50 different DNA elements into the same genomic locus in mouse stem cells. Promoter sequences of approximately 1,000 bp autonomously recapitulated correct DNA methylation in pluripotent cells. Moreover, they supported proper de novo methylation during differentiation. Truncation analysis revealed that this regulatory potential is contained within small methylation-determining regions (MDRs). MDRs can mediate both hypomethylation and de novo methylation in cis, and their activity depends on developmental state, motifs for DNA-binding factors and a critical CpG density. These results demonstrate that proximal sequence elements are both necessary and sufficient for regulating DNA methylation and reveal basic constraints of this regulation.