Comment on "Theory and computer simulation for the equation of state of additive hard-disk fluid mixtures"

A flaw in the comparison between two different theoretical equations of state for a binary mixture of additive hard disks and Monte Carlo results, as recently reported in C. Barrio and J. R. Solana, Phys. Rev. E 63, 011201 (2001), is pointed out. It is found that both proposals, which require the equation of state of the single component system as input, lead to comparable accuracy but the one advocated by us [A. Santos, S. B. Yuste, and M. L\'{o}pez de Haro, Mol. Phys. 96, 1 (1999)] is simpler and complies with the exact limit in which the small disks are point particles.Comment: 4 pages, including 1 figur

Demixing can occur in binary hard-sphere mixtures with negative non-additivity

A binary fluid mixture of non-additive hard spheres characterized by a size ratio $\gamma=\sigma_2/\sigma_1<1$ and a non-additivity parameter $\Delta=2\sigma_{12}/(\sigma_1+\sigma_2)-1$ is considered in infinitely many dimensions. From the equation of state in the second virial approximation (which is exact in the limit $d\to\infty$) a demixing transition with a critical consolute point at a packing fraction scaling as $\eta\sim d 2^{-d}$ is found, even for slightly negative non-additivity, if $\Delta>-{1/8}(\ln\gamma)^2$. Arguments concerning the stability of the demixing with respect to freezing are provided.Comment: 4 pages, 2 figures; title changed; final paragraph added; to be published in PRE as a Rapid Communicatio

Simple equation of state for hard disks on the hyperbolic plane

A simple equation of state for hard disks on the hyperbolic plane is proposed. It yields the exact second virial coefficient and contains a pole at the highest possible packing. A comparison with another very recent theoretical proposal and simulation data is presented.Comment: 3 pages, 1 figur

Are beryllium abundances anomalous in stars with giant planets?

In this paper we present beryllium (Be) abundances in a large sample of 41 extra-solar planet host stars, and for 29 stars without any known planetary-mass companion, spanning a large range of effective temperatures. The Be abundances were derived through spectral synthesis done in standard Local Thermodynamic Equilibrium, using spectra obtained with various instruments. The results seem to confirm that overall, planet-host stars have ``normal'' Be abundances, although a small, but not significant, difference might be present. This result is discussed, and we show that this difference is probably not due to any stellar ``pollution'' events. In other words, our results support the idea that the high-metal content of planet-host stars has, overall, a ``primordial'' origin. However, we also find a small subset of planet-host late-F and early-G dwarfs that might have higher than average Be abundances. The reason for the offset is not clear, and might be related either to the engulfment of planetary material, to galactic chemical evolution effects, or to stellar-mass differences for stars of similar temperature.Comment: 15 pages, 9 figures, accepted for publication in Astronomy & Astrophysic

Requirement of a Plasmid-Encoded Catalase for Survival of \u3cem\u3eRhizobium etli\u3c/em\u3e CFN42 in a Polyphenol-Rich Environment

Nitrogen-fixing bacteria collectively called rhizobia are adapted to live in polyphenol-rich environments. The mechanisms that allow these bacteria to overcome toxic concentrations of plant polyphenols have not been clearly elucidated. We used a crude extract of polyphenols released from the seed coat of the black bean to simulate a polyphenol-rich environment and analyze the response of the bean-nodulating strain Rhizobium etli CFN42. Our results showed that the viability of the wild type as well as that of derivative strains cured of plasmids p42a, p42b, p42c, and p42d or lacking 200 kb of plasmid p42e was not affected in this environment. In contrast, survival of the mutant lacking plasmid p42f was severely diminished. Complementation analysis revealed that the katG gene located on this plasmid, encoding the only catalase present in this bacterium, restored full resistance to testa polyphenols. Our results indicate that oxidation of polyphenols due to interaction with bacterial cells results in the production of a high quantity of H2O2, whose removal by the katG-encoded catalase plays a key role for cell survival in a polyphenol-rich environment

The benefit of multisensory integration with biological motion signals

Assessing intentions, direction, and velocity of others is necessary for most daily tasks, and such information is often made available by both visual and auditory motion cues. Therefore, it is not surprising our great ability to perceive human motion. Here, we explore the multisensory integration of cues of biological motion walking speed. After testing for audiovisual asynchronies (visual signals led auditory ones by 30ms in simultaneity temporal windows of 76.4ms), in the main experiment, visual, auditory, and bimodal stimuli were compared to a standard audiovisual walker in a velocity discrimination task. Results in variance reduction conformed to optimal integration of congruent bimodal stimuli across all subjects. Interestingly, the perceptual judgments were still close to optimal for stimuli at the smallest level of incongruence. Comparison of slopes allows us to estimate an integration window of about 60ms, which is smaller than that reported in audiovisual speech.This work was partly funded by the Portuguese Foundation for Science and Technology (SFRH/BD/36345/2007, PTDC/SAU-BEB/68455/2006, SFRH/BSAB/974/2009) and the Portugal-Spain Actions PT2009-0186 from the Spanish Government and E-134/10 from the Portuguese Conselho de Reitores das Universidades Portuguesas

The time to passage of biological and complex motion

A significant part of human interactions occur with other human beings and not only with inanimate objects. It is important in everyday tasks to estimate the time it takes other people to reach (time to contact) or pass us (time to passage). Surprisingly, little is known about judging time to contact or time to passage of biological or other complex motions. In two experiments, rigid and non-rigid (biological, inverted, scrambled, and complex non-biological) motion conditions were compared in a time-to-passage judgment task. Subjects could judge time to passage of point-light-walker displays. However, due to relative and opponent movements of body parts, all articulated patterns conveyed a noisier looming pattern. Non-rigid stimuli were judged as passing sooner than rigid stimuli but reflected more uncertainty in the judgments as revealed by precision judgments and required longer reaction times. Our findings suggested that perceptual judgments for complex motion, including biological patterns, are built on top of the same processing channels that are involved on rigid motion perception. The complexity of the motion pattern (rigid vs. non-rigid) plays a more determinant role than the "biologicity" of the stimulus (biological vs. non-biological), at least concerning time-to-passage judgments

The time to passage of biological and complex motion

A significant part of human interactions occur with other human beings and not only with inanimate objects. It is important in everyday tasks to estimate the time it takes other people to reach (time to contact) or pass us (time to passage). Surprisingly, little is known about judging time to contact or time to passage of biological or other complex motions. In two experiments, rigid and non-rigid (biological, inverted, scrambled, and complex non-biological) motion conditions were compared in a time-to-passage judgment task. Subjects could judge time to passage of point-light-walker displays. However, due to relative and opponent movements of body parts, all articulated patterns conveyed a noisier looming pattern. Non-rigid stimuli were judged as passing sooner than rigid stimuli but reflected more uncertainty in the judgments as revealed by precision judgments and required longer reaction times. Our findings suggested that perceptual judgments for complex motion, including biological patterns, are built on top of the same processing channels that are involved on rigid motion perception. The complexity of the motion pattern (rigid vs. non-rigid) plays a more determinant role than the “biologicity” of the stimulus (biological vs. non-biological), at least concerning time-to-passage judgments.Luso-Spanish Integrated Action funded by the Spanish and Portuguese governmentsFundação para a Ciência e a Tecnologia (FCT