The U.N. Contribution to Future International Security

The most important fact with which planners and policy makers have had to contend over the last two years is that the end of the Cold War removed from the international political system its central dominating principle-the East-West dispute. [n a speech last year, President Bush outlined his vision of a new framework in the following words: The new world order does not mean surrendering our sovereignty or forfeiting our interests. It really describes a responsibility imposed by our successes. It refers to new ways of working with other nations to deter aggression and to achieve stability, to achieve prosperity, and above all, to achieve peace. It springs from hopes for a world based on a shared commitment to a set of principles that undergird our relations-peaceful settlement of disputes, solidarity against aggression, reduced and controlled arsenals, and just treatment of peoples

Jago Pakistan/ Wake Up, Pakistan: The Report of the Century Foundation International Working Group on Pakistan

The time is long past for Pakistan to wake up to its present predicament and begin a serious reassessment of the fundamental policy challenges it faces. Decades of mistakes and misperceptions have compounded pernicious ideological choices to present Pakistani society with a series of ongoing crises it must address before its basic resilience is overwhelmed: a public sphere dominated by extremists, a crippled economy debilitated by corruption, and a deteriorating regional position. The Century Foundation International Working Group on Pakistan, comprised of a broad and diverse assemblage of American, Pakistani and international figures deeply concerned about the country's future, believes it is time for Pakistan to address these problems vigorously and comprehensively, and for its international partners to assist where they can

PrFeO3 Photocathodes Prepared Through Spray Pyrolysis

Perovskite oxides are receiving wide interest for photocatalytic and photoelectrochemical devices, owing to their suitable band gaps for solar light absorption and stability in aqueous applications. Herein, we assess the activity of PrFeO3 photocathodes prepared by using spray pyrolysis and calcination temperatures between 500 and 700 °C. Scanning electron microscopy shows corrugated films of high surface coverage on the conductive glass substrate. The electrochemically active surface area shows slight decreases with temperature increases from 500 to 600 and 700 °C. However, transient photocurrent responses and impedance spectroscopy data showed that films calcined at higher temperatures reduced the probabilities of recombination due to trap states, resulting in faster rates of charge extraction. In this trade‐off, a calcination temperature of 600 °C provided a maximum photocurrent of ‐130±4 μA cm−2 at +0.43 VRHE under simulated sunlight, with an incident photon‐to‐current conversion efficiency of 6.6 % at +0.61 VRHE and 350 nm and an onset potential of +1.4 VRHE for cathodic photocurrent

Pathogen burden, inflammation, proliferation and apoptosis in human in-stent restenosis - Tissue characteristics compared to primary atherosclerosis

Pathogenic events leading to in-stent restenosis (ISR) are still incompletely understood. Among others, inflammation, immune reactions, deregulated cell death and growth have been suggested. Therefore, atherectomy probes from 21 patients with symptomatic ISR were analyzed by immunohistochemistry for pathogen burden and compared to primary target lesions from 20 stable angina patients. While cytomegalovirus, herpes simplex virus, Epstein-Barr virus and Helicobacter pylori were not found in ISR, acute and/or persistent chlamydial infection were present in 6/21 of these lesions (29%). Expression of human heat shock protein 60 was found in 8/21 of probes (38%). Indicated by distinct signals of CD68, CD40 and CRP, inflammation was present in 5/21 (24%), 3/21 (14%) and 2/21 (10%) of ISR cases. Cell density of ISR was significantly higher than that of primary lesions ( 977 +/- 315 vs. 431 +/- 148 cells/mm(2); p < 0.001). There was no replicating cell as shown by Ki67 or PCNA. TUNEL+ cells indicating apoptosis were seen in 6/21 of ISR specimens (29%). Quantitative analysis revealed lower expression levels for each intimal determinant in ISR compared to primary atheroma (all p < 0.05). In summary, human ISR at the time of clinical presentation is characterized by low frequency of pathogen burden and inflammation, but pronounced hypercellularity, low apoptosis and absence of proliferation. Copyright (C) 2004 S. Karger AG, Basel

Late Quaternary Sedimentary Record and Holocene Channel Avulsions of the Jamuna and Old Brahmaputra River Valleys in the Upper Bengal Delta Plain

The first Holocene stratigraphic record of river-channel occupation and switching between the Brahmaputra–Jamuna and Old Brahmaputra paleovalleys is presented here. Motivated by the Brahmaputra River's historic avulsion from the Old Brahmaputra channel to its present-day Jamuna course, we have obtained sediment and radiocarbon samples from 41 boreholes along a 120 km transect crossing these two braided-river valleys. The stratigraphy along this transect reveals sand-dominated Holocene channel systems, each bound by remnant, mud-capped Pleistocene stratigraphy. Using sediment lithology and bulk strontium concentration as a provenance indicator, we define the geometry and channel-occupation history of each paleovalley. The western Brahmaputra–Jamuna valley is broad and somewhat deeper compared with the Old Brahmaputra valley, the latter actually comprising a composite of two narrower sub-valleys bifurcated by an antecedent topographic remnant. The gently sloped valley margins (slope: 0.002 to 0.007) and high width-to-thickness ratio (W/T: ~ 1000) of the Brahmaputra–Jamuna valley suggest that it was filled primarily through lateral channel migration and the reworking of braidbelt and overbank deposits. Conversely, the two Old Brahmaputra sub-valleys have comparatively steeper valley margins (slope: 0.007 to 0.022) and lower width-to-thickness ratios (W/T: ~ 125 and ~ 250), indicating that these were filled primarily through vertical aggradation of channel sands. We attribute this disparity in valley geometry and fill processes to the different occupation histories for each valley. In this case, the much larger Brahmaputra–Jamuna valley represents the principal, if not singular, river course during the last lowstand of sea-level, with a prominent gravel lag underlying the valley. In contrast the smaller Old Brahmaputra valleys do not appear to have been present, or at least well developed, at the last lowstand. Rather these courses were first occupied during the early Holocene transgression, and we infer that the river had been previously excluded from this region by the relatively higher elevation between the Madhupur Terrace and the Shillong Massif. We also demonstrate that the Brahmaputra River experienced 3–4 major avulsions during the Holocene, with considerably longer occupation times within the principal Brahmaputra–Jamuna valley. Together these observations indicate that occupation history and antecedent topography have been important controls on river course mobility and avulsion behavior

Multiplexed Immunoassay Panel Identifies Novel CSF Biomarkers for Alzheimer's Disease Diagnosis and Prognosis

Clinicopathological studies suggest that Alzheimer's disease (AD) pathology begins ∼10-15 years before the resulting cognitive impairment draws medical attention. Biomarkers that can detect AD pathology in its early stages and predict dementia onset would, therefore, be invaluable for patient care and efficient clinical trial design. We utilized a targeted proteomics approach to discover novel cerebrospinal fluid (CSF) biomarkers that can augment the diagnostic and prognostic accuracy of current leading CSF biomarkers (Aβ42, tau, p-tau181).Using a multiplexed Luminex platform, 190 analytes were measured in 333 CSF samples from cognitively normal (Clinical Dementia Rating [CDR] 0), very mildly demented (CDR 0.5), and mildly demented (CDR 1) individuals. Mean levels of 37 analytes (12 after Bonferroni correction) were found to differ between CDR 0 and CDR>0 groups. Receiver-operating characteristic curve analyses revealed that small combinations of a subset of these markers (cystatin C, VEGF, TRAIL-R3, PAI-1, PP, NT-proBNP, MMP-10, MIF, GRO-α, fibrinogen, FAS, eotaxin-3) enhanced the ability of the best-performing established CSF biomarker, the tau/Aβ42 ratio, to discriminate CDR>0 from CDR 0 individuals. Multiple machine learning algorithms likewise showed that the novel biomarker panels improved the diagnostic performance of the current leading biomarkers. Importantly, most of the markers that best discriminated CDR 0 from CDR>0 individuals in the more targeted ROC analyses were also identified as top predictors in the machine learning models, reconfirming their potential as biomarkers for early-stage AD. Cox proportional hazards models demonstrated that an optimal panel of markers for predicting risk of developing cognitive impairment (CDR 0 to CDR>0 conversion) consisted of calbindin, Aβ42, and age.Using a targeted proteomic screen, we identified novel candidate biomarkers that complement the best current CSF biomarkers for distinguishing very mildly/mildly demented from cognitively normal individuals. Additionally, we identified a novel biomarker (calbindin) with significant prognostic potential

StrainGE: A toolkit to track and characterize low-abundance strains in complex microbial communities

Human-associated microbial communities comprise not only complex mixtures of bacterial species, but also mixtures of conspecific strains, the implications of which are mostly unknown since strain level dynamics are underexplored due to the difficulties of studying them. We introduce the Strain Genome Explorer (StrainGE) toolkit, which deconvolves strain mixtures and characterizes component strains at the nucleotide level from short-read metagenomic sequencing with higher sensitivity and resolution than other tools. StrainGE is able to identify strains at 0.1x coverage and detect variants for multiple conspecific strains within a sample from coverages as low as 0.5x