The asymptotic iteration method for the angular spheroidal eigenvalues with arbitrary complex size parameter c

The asymptotic iteration method is applied, to calculate the angular spheroidal eigenvalues $\lambda^{m}_{\ell}(c)$ with arbitrary complex size parameter $c$. It is shown that, the obtained numerical results of $\lambda^{m}_{\ell}(c)$ are all in excellent agreement with the available published data over the full range of parameter values $\ell$, $m$, and $c$. Some representative values of $\lambda^{m}_{\ell}(c)$ for large real $c$ are also given.Comment: 15 pages, 1 figur

Magnetism in Gd-W films

Vapor condensation techniques are useful to prepare magnetic alloys whose components have low or even negligible equilibrium mutual solubility. In this work, one of these techniques-sputtering-was used to obtain Gd(x)W(1-x) alloys whose magnetic properties were investigated as a function of the Gd atomic concentration x. Gadolinium and various Gd-based alloys are promising materials for magnetic refrigeration and this was one of the motivations for this study. The Gd(x)-W(1-x) films were sputter deposited from Gd and W targets with x ranging from 0 to 1 as determined by x-ray energy-dispersive spectroscopic analyses. X-ray diffraction patterns indicate that crystalline structures were formed at low and high Gd concentrations, while at intermediate concentrations, the films were amorphous. Magnetization measurements, performed as a function of temperature and with static and alternating applied fields, reveal a spin glasslike behavior in all the W-containing samples for temperatures below the freezing temperature T(f). For low and intermediate Gd concentrations, and for T>T(f), the films were paramagnetic, while a ferromagnetic phase was observed in the Gd-W alloy of the highest Gd content. The magnetocaloric effect was investigated from the magnetization isotherms M versus H, from which the isothermal magnetic entropy variation Delta S(M) as a function of T, for the removal of an applied field of 50 kOe, was determined. It was observed that the maximum value of Delta S(M) for each Delta S(M) versus T curve and the temperature at which these maxima occur, are strongly dependent on x. (C) 2008 American Institute of Physics.103

Push-pull farming systems

Farming systems for pest control, based on the stimulo-deterrent diversionary strategy or push–pull system, have become an important target for sustainable intensification of food production. A prominent example is push–pull developed in sub-Saharan Africa using a combination of companion plants delivering semiochemicals, as plant secondary metabolites, for smallholder farming cereal production, initially against lepidopterous stem borers. Opportunities are being developed for other regions and farming ecosystems. New semiochemical tools and delivery systems, including GM, are being incorporated to exploit further opportunities for mainstream arable farming systems. By delivering the push and pull effects as secondary metabolites, for example, (E)-4,8-dimethyl-1,3,7-nonatriene repelling pests and attracting beneficial insects, problems of high volatility and instability are overcome and compounds are produced when and where required

Endomyocardial Fibrosis: Still a Mystery after 60 Years

The pathologist Jack N. P. Davies identified endomyocardial fibrosis in Uganda in 1947. Since that time, reports of this restrictive cardiomyopathy have come from other parts of tropical Africa, South Asia, and South America. In Kampala, the disease accounts for 20% of heart disease patients referred for echocardiography. We conducted a systematic review of research on the epidemiology and etiology of endomyocardial fibrosis. We relied primarily on articles in the MEDLINE database with either “endomyocardial fibrosis” or “endomyocardial sclerosis” in the title. The volume of publications on endomyocardial fibrosis has declined since the 1980s. Despite several hypotheses regarding cause, no account of the etiology of this disease has yet fully explained its unique geographical distribution

IL10 Haplotype Associated with Tuberculin Skin Test Response but Not with Pulmonary TB

Evidence from genetic association and twin studies indicates that susceptibility to tuberculosis (TB) is under genetic control. One gene implicated in susceptibility to TB is that encoding interleukin-10 (IL10). In a group of 2010 Ghanaian patients with pulmonary TB and 2346 healthy controls exposed to Mycobacterium tuberculosis, among them 129 individuals lacking a tuberculin skin test (PPD) response, we genotyped four IL10 promoter variants at positions −2849 , −1082 , −819 , and −592 and reconstructed the haplotypes. The IL10 low-producer haplotype −2849A/−1082A/−819C/−592C, compared to the high-producer haplotype −2849G/−1082G/−819C/−592C, occurred less frequent among PPD-negative controls than among cases (OR 2.15, CI 1.3–3.6) and PPD-positive controls (OR 2.09, CI 1.2–3.5). Lower IL-10 plasma levels in homozygous −2849A/−1082A/−819C/−592C carriers, compared to homozygous −2849G/−1082G/−819C/−592C carriers, were confirmed by a IL-10 ELISA (p = 0.016). Although we did not observe differences between the TB patients and all controls, our results provide evidence that a group of individuals exposed to M. tuberculosis transmission is genetically distinct from healthy PPD positives and TB cases. In these PPD-negative individuals, higher IL-10 production appears to reflect IL-10-dependent suppression of adaptive immune responses and sustained long-term specific anergy

Causal Pathways from Enteropathogens to Environmental Enteropathy: Findings from the MAL-ED Birth Cohort Study

Background Environmental enteropathy (EE), the adverse impact of frequent and numerous enteric infections on the gut resulting in a state of persistent immune activation and altered permeability, has been proposed as a key determinant of growth failure in children in low- and middle-income populations. A theory-driven systems model to critically evaluate pathways through which enteropathogens, gut permeability, and intestinal and systemic inflammation affect child growth was conducted within the framework of the Etiology, Risk Factors and Interactions of Enteric Infections and Malnutrition and the Consequences for Child Health and Development (MAL-ED) birth cohort study that included children from eight countries. Methods Non-diarrheal stool samples (N = 22,846) from 1253 children from multiple sites were evaluated for a panel of 40 enteropathogens and fecal concentrations of myeloperoxidase, alpha-1-antitrypsin, and neopterin. Among these same children, urinary lactulose:mannitol (L:M) (N = 6363) and plasma alpha-1-acid glycoprotein (AGP) (N = 2797) were also measured. The temporal sampling design was used to create a directed acyclic graph of proposed mechanistic pathways between enteropathogen detection in non-diarrheal stools, biomarkers of intestinal permeability and inflammation, systemic inflammation and change in length- and weight- for age in children 0–2 years of age. Findings Children in these populations had frequent enteric infections and high levels of both intestinal and systemic inflammation. Higher burdens of enteropathogens, especially those categorized as being enteroinvasive or causing mucosal disruption, were associated with elevated biomarker concentrations of gut and systemic inflammation and, via these associations, indirectly associated with both reduced linear and ponderal growth. Evidence for the association with reduced linear growth was stronger for systemic inflammation than for gut inflammation; the opposite was true of reduced ponderal growth. Although Giardia was associated with reduced growth, the association was not mediated by any of the biomarkers evaluated. Interpretation The large quantity of empirical evidence contributing to this analysis supports the conceptual model of EE. The effects of EE on growth faltering in young children were small, but multiple mechanistic pathways underlying the attribution of growth failure to asymptomatic enteric infections had statistical support in the analysis. The strongest evidence for EE was the association between enteropathogens and linear growth mediated through systemic inflammation