Light source position and reflectance estimation from a single view without the distant illumination assumption

Several techniques have been developed for recovering reflectance properties of real surfaces under unknown illumination. However, in most cases, those techniques assume that the light sources are located at infinity, which cannot be applied safely to, for example, reflectance modeling of indoor environments. In this paper, we propose two types of methods to estimate the surface reflectance property of an object, as well as the position of a light source from a single view without the distant illumination assumption, thus relaxing the conditions in the previous methods. Given a real image and a 3D geometric model of an object with specular reflection as inputs, the first method estimates the light source position by fitting to the Lambertian diffuse component, while separating the specular and diffuse components by using an iterative relaxation scheme. Our second method extends that first method by using as input a specular component image, which is acquired by analyzing multiple polarization images taken from a single view, thus removing its constraints on the diffuse reflectance property. This method simultaneously recovers the reflectance properties and the light source positions by optimizing the linearity of a log-transformed Torrance-Sparrow model. By estimating the object's reflectance property and the light source position, we can freely generate synthetic images of the target object under arbitrary lighting conditions with not only source direction modification but also source-surface distance modification. Experimental results show the accuracy of our estimation framework.     

On the rheology of packed polymer powders

The rheology of polystyrene powder beds was examined by two kinds of experiments. From stress relaxation measurements during powder compaction, it was found that relaxation at the shorter times could be attributed to sliding between particles. This is followed by a relaxation attributed to the deformation of the polystyrene particles themselves. From dynamic mechanical measurements, an increase was found in the value of vibrational absorption coefficient (Q^?1 value) at a temperature below that of the main relaxation dispersion of bulk polystyrene, attributed to the slipping around tight particle junctions. These phenomena appear characteristic of powder-like materials.     

Analysis of upgraded solvent-refined coal (SRC) liquid products

Upgraded coal-derived liquids obtained from catalytic hydroprocessing of a 30–70(wt%) blend of SRC-1 with SRC-II have been studied by infrared and proton magnetic resonance spectroscopy, and gel permeation chromatography techniques. Compared with the feed blend, the upgraded liquids exhibit a lower C/H ratio and decreased aromatic, heteroatom and pentane-insoluble contents, along with decreased specific gravity and viscosity. The amount of hydrogen-bonded structure in the upgraded liquid decreases with increases in residence time and processing temperature. The pseudo-first-order disappearance of phenolic OH and total nitrogen during processing indicates a relative reactivity of 2:1 of hydroxyl oxygen removal to total nitrogen removal in the upgrading process. Conversion of pentaneinsolubles to soluble oil also follows a pseudo-first-order reaction; under mild processing conditions, the heteroatom functionalities play a dominant role in the ease and extent of this conversion. Higher temperatures increase thermal cracking and hydrocracking of the ring structure resulting in more conversion of asphaltene to oil. The linear dependence of the logarithm of viscosity on the content of heteroatoms and toluene-insolubles (TI) indicates the importance of molecular interactions involving polar functional groups in defining the viscosity of coal-derived liquid.     

Genomic footprinting of the yeast zinc finger protein Rme1p and its roles in repression of the meiotic activator IME1

The zinc finger protein Rme1p is a negative regulator of the meiotic activator IME1 in Saccharomyces cerevisiae . Prior studies have shown that Rme1p binds in vitro to a site near nt -2030 in the IME1 upstream region, but a genomic mutation in that site has little effect on repression of IME1 . To identify Rme1p binding sites in vivo , we have examined the binding of Rme1p to genomic sites through in vivo footprinting. We show that Rme1p binds to two sites in the IME1 upstream region, near nt -1950 and -2030. Mutations in both binding sites abolish repression of chromosomal IME1 by Rme1p, whereas a mutation in either single site causes partial derepression. Therefore, both Rme1p binding sites are essential for repression of IME1 . Prior studies have shown that repression by Rme1p depends upon RGR1 and SIN4 , which specify RNA polymerase II mediator subunits that are required for normal nucleosome density. We find that RGR1 and SIN4 are not simply required for Rme1p to bind to DNA in vivo . These results suggest that Rme1p functions directly as a repressor of IME1 and that Rgr1p and Sin4p are required for DNA-bound Rme1p to exert repression.     

Hankel norm of sampled-data systems

Generalizes the concept of Hankel norm for purely continuous-time systems to sampled-data systems. The Hankel norm of a sampled-data system is defined by taking into account intersample behaviors. The formula of the Hankel norm of a sampled-data system is given by a hybrid state-space model approach. The authors show that the Hankel norm is equal to that of an equivalent discrete-time system. Two simple examples including sampled-data controller reduction are demonstrated