3D short-range wetting and nonlocality

Analysis of a microscopic Landau-Ginzburg-Wilson model of 3D short-ranged wetting shows that correlation functions are characterized by two length scales, not one, as previously thought. This has a simple diagrammatic explanation using a nonlocal interfacial Hamiltonian and yields a thermodynamically consistent theory of wetting in keeping with exact sum rules. For critical wetting the second length serves to lower the cutoff in the spectrum of interfacial fluctuations determining the repulsion from the wall. We show how this corrects previous renormalization group predictions for fluctuation effects, based on local interfacial Hamiltonians. In particular, lowering the cutoff leads to a substantial reduction in the effective value of the wetting parameter and prevents the transition being driven first order. Quantitative comparison with Ising model simulation studies due to Binder, Landau, and co-workers is also mad

Population genetic structure of N. American and European \u3ci\u3ePhalaris arundinacea\u3c/i\u3e L. as inferred from inter-simple sequence repeat markers

Phalaris arundinacea L. (reed canarygrass) has become one of the most aggressive invaders of North American wetlands. P. arundinacea is native to temperate N. America, Europe, and Asia, but repeated introductions of European genotypes to N. America, recent range expansions, and the planting of forage and ornamental cultivars complicate the resolution of its demographic history. Molecular tools can help to unravel the demographic and invasion history of populations of invasive species. In this study, inter-simple sequence repeat markers were used to analyze the population genetic structure of European and N. American populations of reed canary grass as well as forage and ornamental cultivars. We found that P. arundinacea harbors a high amount of genetic diversity with most of the diversity located within, as opposed to among, populations. Cluster analyses suggested that current populations are admixtures of two formerly distinct genetic groups

An HST/WFPC2 Snapshot Survey of 2MASS-Selected Red QSOs

Using simple infrared color selection, 2MASS has found a large number of red, previously unidentified, radio-quiet QSOs. Although missed by UV/optical surveys, the 2MASS QSOs have K-band luminosities that are comparable to "classical" QSOs. This suggests the possible discovery of a previously predicted large population of dust-obscured radio-quiet QSOs. We present the results of an imaging survey of 29 2MASS QSOs observed with WFPC2 onboard the Hubble Space Telescope. I-band images, which benefit from the relative faintness of the nuclei at optical wavelengths, are used to characterize the host galaxies, measure the nuclear contribution to the total observed I-band emission, and to survey the surrounding environments. The 2MASS QSOs are found to lie in galaxies with a variety of morphologies, luminosities, and dynamical states, not unlike those hosting radio-quiet PG QSOs. Our analysis suggests that the extraordinary red colors of the 2MASS QSOs are caused by extinction of an otherwise typical QSO spectrum due to dust near the nucleus.Comment: 23 pages including 9 figures and 7 tables, accepted for publication in ApJ, higher resolution HST images at: http://shapley.as.arizona.edu/~amarble/papers/twomq

Peroxiredoxin Catalysis at Atomic Resolution

Peroxiredoxins (Prxs) are ubiquitous cysteine-based peroxidases that guard cells against oxidative damage, are virulence factors for pathogens, and are involved in eukaryotic redox regulatory pathways. We have analyzed catalytically active crystals to capture atomic resolution snapshots of a PrxQ-subfamily enzyme (from Xanthomonas campestris) proceeding through thiolate, sulfenate, and sulfinate species. These analyses provide structures of unprecedented accuracy for seeding theoretical studies, and show novel conformational intermediates giving insight into the reaction pathway. Based on a highly non-standard geometry seen for the sulfenate intermediate, we infer that the sulfenate formation itself can strongly promote local unfolding of the active site to enhance productive catalysis. Further, these structures reveal that preventing local unfolding, in this case via crystal contacts, results in facile hyperoxidative inactivation even for Prxs normally resistant to such inactivation. This supports previous proposals that conformation-specific inhibitors may be useful for achieving selective inhibition of Prxs that are drug targets

Examination of the reliability and factor structure of the Autism Spectrum Quotient (AQ) in a non-clinical sample

A self-report screening measure for high functioning autism spectrum disorders is needed for diagnostic screening and research purposes. The Autism Spectrum Quotient (AQ) has been developed for these reasons, although a comprehensive assessment of the psychometric properties of the AQ has not been completed. The purpose of the current study was to assess the distribution, internal consistency, and factor structure of the AQ in a non-clinical sample (n = 1005). The current findings demonstrate the normal distribution of autistic traits and support a three-factor structure of the AQ. Additionally, a three-factor version of the AQ yielded somewhat improved internal consistency. Implications of these findings and suggestions for further development of the AQ as a measure of the autism spectrum are offered

Compensating for source directivity in immersive wave experimentation

ISSN:0001-4966ISSN:1520-852

The interaction of reinforcement sensitivity and life events in the prediction of anhedonic depression and mixed anxiety-depression symptoms

This study examined the relationship between reinforcement sensitivity theory (RST), life stress, and internalizing symptoms. Generally, low sensitivity of the behavioral approach system (BAS) predicts depression whereas high sensitivity of the behavioral inhibition system (BIS) predicts anxiety and depression. However, few studies have examined how RST variables interact with life stress to predict these symptoms. It was hypothesized that higher BIS sensitivity would predict greater anxious arousal; lower BAS sensitivity and higher BIS sensitivity would predict greater anhedonic depression as predicted by the joint subsystems hypothesis (JSH); and low BAS, high BIS, and high life stress would interact to predict anhedonic depression symptoms whereas high BIS with high life stress would predict anxious symptoms. A sample of 285 undergraduates completed measures of RST, life stress, and internalizing symptoms. Greater BIS sensitivity predicted mixed anxiety–depression and anhedonic depressed symptoms, lower BAS predicted anhedonic depression symptoms, and life events predicted mixed anxiety–depression. Three-way interactions indicated that for high life stress, BIS predicted both types of symptoms. For low life stress, low BAS and high BIS predicted anhedonic depression whereas high BIS and high BAS predicted mixed anxiety–depression. The implications of these findings are discussed in terms of the JSH

Human use pharmaceuticals in the estuarine environment: a survey of the Chesapeake Bay, Biscayne Bay, and Gulf of the Farallones

The assessment of emerging risks in the aquatic environment is a major concern and focus of environmental science (Daughton and Ternes, 1999). One significant class of chemicals that has received relatively little attention until recently are the human use pharmaceuticals. In 2004, an estimated 2.6 billion prescriptions were written for the top 300 pharmaceuticals in the U.S. (RxList, 2005). Mellon et al. (2001) estimated that 1.4 million kg of antimicrobials are used in human medicine every year. The use of pharmaceuticals is also estimated to be on par with agrochemicals (Daughton and Ternes, 1999). Unlike agrochemicals (e.g., pesticides) which tend to be delivered to the environment in seasonal pulses, pharmaceuticals are continuously released through the use/excretion and disposal of these chemicals, which may produce the same exposure potential as truly persistent pollutants. Human use pharmaceuticals can enter the aquatic environment through a number of pathways, although the main one is thought to be via ingestion and subsequent excretion by humans (Thomas and Hilton, 2004). Unused pharmaceuticals are typically flushed down the drain or wind up in landfills (Jones et al. 2001)