Sex‐specific and dose‐response relationships of urinary cobalt and molybdenum levels with glucose levels and insulin resistance in U.S. adults

Growing studies have linked metal exposure to diabetes risk. However, these studies had inconsistent results. We used a multiple linear regression model to investigate the sex-specific and dose-response associations between urinary metals (cobalt (Co) and molybdenum (Mo)) and diabetes-related indicators (fasting plasma glucose (FPG), hemoglobin A1c (HbA1c), homeostasis model assessment for insulin resistance (HOMA-IR), and insulin) in a cross-sectional study based on the United States National Health and Nutrition Examination Survey. The urinary metal concentrations of 1423 eligible individuals were stratified on the basis of the quartile distribution. Our results showed that the urinary Co level in males at the fourth quartile (Q4) was strongly correlated with increased FPG (β = 0.61, 95% CI: 0.17–1.04), HbA1c (β = 0.31, 95% CI: 0.09–0.54), insulin (β = 8.18, 95% CI: 2.84–13.52), and HOMA–IR (β = 3.42, 95% CI: 1.40–5.44) when compared with first quartile (Q1). High urinary Mo levels (Q4 vs. Q1) were associated with elevated FPG (β = 0.46, 95% CI: 0.17–0.75) and HbA1c (β = 0.27, 95% CI: 0.11–0.42) in the overall population. Positive linear dose-response associations were observed between urinary Co and insulin (P_nonlinear = 0.513) and HOMA–IR (P_nonlinear = 0.736) in males, as well as a positive linear dose-response relationship between urinary Mo and FPG (P_nonlinear = 0.826) and HbA1c (P_nonlinear = 0.376) in the overall population. Significant sex-specific and dose-response relationships were observed between urinary metals (Co and Mo) and diabetes-related indicators, and the potential mechanisms should be further investigated.     

Nickel accumulation and its effect on biomass, protein content and antioxidative enzymes in roots and leaves of watercress （Nasturtium officinale R. Br.）

In order to understand its response towards nickel stress, watercress (Nasturtium o cinale R. Br.) was exposed to nickel (1–25 mg/L) for 1, 3, 5 and 7 days. The accumulation and translocation of nickel were determined and the influence of nickel on biomass, protein content and enzymatic antioxidants was examined for both roots and leaves. It was determined that N. o cinale could accumulate appreciable amounts of Ni in both roots and leaves. Nickel accumulated particularly in the roots of plants. Biomass increased at low nickel concentrations but certain measurable change was not found at high concentrations. Under stress conditions the antioxidant enzymes were up-regulated compared to control. An increase in protein content and enzyme activities was observed at moderate exposure conditions followed by a decline at both roots and leaves. The maximum enzyme activities were observed at di erent exposure conditions. Our results showed that N. o cinale had the capacity to overcome nickel-induced stress especially at moderate nickel exposure. Therefore, N. o cinale may be used as a phytoremediator in moderately polluted aquatic ecosystems.     

Transport and deposition of indoor radon decay products—I. Model development and validation

Commonly used mathematical models of indoor radon decay product behavior are based on macroscopic mass-balances, often referred to as ‘uniformly-mixed models’. The uniformly-mixed model's applicability is limited by its inability to track the movement of pollutants from their sources to other areas within the enclosure, to permit spatial- or time-dependent sources, or to take proper account of interactions with macroscopic surfaces. Although the uniformly-mixed model parameterizes the deposition process as a constant volumetric removal rate, in reality the deposition process is actually a surface phenomenon and is strongly affected by environmental conditions.This paper describes the development of RADTRAN, a two-dimensional radon progeny transport model that begins with the differential conservation equations describing the motion of air and the transport of reactive pollutants, introduces appropriate boundary conditions to represent surface deposition, and then calculates the concentration distribution of radon progeny throughout the entire region of interest. Knowing the concentration gradient near the surface, a local mass-transfer coefficient (the deposition velocity) can be determined as a function of environmental conditions. RADTRAN simulations have been based on several flow conditions: buoyancy-driven recirculating enclosure flows, free and forced-convection boundary layer flows, and one-dimensional diffusion. Free progeny diffusivity, D^f, and attachment rate, X, were varied over representative ranges. For these conditions, RADTRAN calculated free deposition velocities of u^f = 0.014–0.079 cm s⁻¹, for ²¹⁸Po. RADTRAN predictions are compared to a range of experimental measurements. It was found that the predicted range of deposition velocities is in rough agreement with findings from experiments conducted in flow conditions similar to the simplified flows used in RADTRAN.     

Levels of airborne man-made mineral fibres in U.K. dwellings. I—Fibre levels during and after installation of insulation

This paper gives the details of airborne levels of man-made mineral fibres (MMMF) found during installation of loft insulation in 12 dwellings. About 250 samples of air were collected and analyzed by transmission electron microscopy (TEM).Respirable fibre levels measured in static samples collected in the lofts during installation generally were < 0.1 f ml⁻¹. In living spaces respirable fibre levels were< 0.006 f ml⁻¹. Personal samples on the installers gave < 1 f ml⁻¹, with the exception of a fine glass fibre blanket. A few selected samples were also analyzed by phase contrast optical microscopy (PCOM) which showed lower values than those recorded by TEM. Static gravimetric concentrations in the lofts were in the 0.3–6.5 mg m⁻³ range, and in the living spaces 0.11–0.44 mg m⁻³, but in both environments most of this dust was not MMMF.     

Levels of airborne man-made mineral fibres in U.K. dwellings. II—Fibre levels during and after some disturbance of loft insulation

In this study airborne levels of MMMF were determined in 11 dwellings during and after disturbance of loft insulation. The disturbance was in two stages.

• 1.(a) Minor disturbance. Household items (such as suitcases) stored in the lofts were moved around for about 10 min. The disturbance to the insulation material was kept to a minimum.
• 2.(b) Major disturbance. Insulation wools were physically handled for about 30 min, simulating the disturbance associated with activities such as rewiring or plumbing.

About 250 samples of air were collected on membrane filters and analyzed by transmission electron microscopy (TEM) in conjunction with energy dispersive X-ray analysis. A few selected samples were analyzed by phase contrast optical microscopy (PCOM). During physical disturbance of the insulation, fibre levels in lofts measured over a 4-h period were up to 0.03 f ml⁻¹. Personal exposure during the disturbance activity was up to 0.2 f ml⁻¹. Contamination of the living space was not detected even though the access door to the loft remained open throughout the disturbance and sampling period.     

Field investigations on the snow chemistry in central and southern california—II. Carbonyls and carboxylic acids

Snow samples from central and southern California were collected during the winter of 1987–1988 from there storms and analyzed for carbonyl compounds and carboxylic acids. Approximately 90% of the samples contained total aldehyde concentrations up to 40 μM. Formaldehyde and acetaldehyde were the dominant aldehydes observed; secondary aldehydes included glyoxal, methylglyoxal, and benzaldehyde. The highest aldehyde concentrations were observed in snow collected in areas where deciduous and coniferous forests are widespread. However, these aldehydes can be attributed also in part to primary and secondary products of anthropogenic activities. Formic and acetic were analyzed in all measured samples with concentrations ranging from 0.5 to 4.9 μM for HCOOH and from <0.3 to 13.4 μM for CH₃COOH. Maximum contribution of organic acids to precipitation-free acidity, calculated by assuming that the only sources of the measured formate and acetate were their respective acid forms, averaged 43.1% for samples with a pH⩽5. A consistent correlation between NH₄⁺ and acetate was found. [CH₃COOH] exceeded [HCOOH] in about 50% of the samples with the highest levels for CH₃COOH measured in cores collected from lower elevated locations adjacent to the Los Angeles basin. Results presented in this paper suggest that dry deposition and/or scavenging of carbonyl compounds and organic acids to snow may be important sinks for these compounds.     

News:Drs.William R.Cullen and Kenneth J.Reimer publish new book “Arsenic is Everywhere:Cause for Concern?”

正Arsenic is Everywhere:Cause for Concern?"This book begins with a discussion of how the word arsenic has a special(and often frightening)place in our society.The book ends with an invitation to dinner where the arsenic content and form of every potential food or beverage is considered.The idea is that while people cannot escape some exposure to arsenic,they     

The relationship between upwind SO2 emissions and SO4– concentrations in precipitation at six sites in the eastern U.S.A.

A method for estimating the upwind SO₂ emissions associated with individual wet SO₄²⁻ deposition events has been developed. The relationship between these estimates and wet SO₄²⁻ concentrations was examined at six Utility Acid Precipitation Study Program Sites (UAPSP) for the 1979–1986 period. Using Spearman correlation coefficients and the Bonferroni experimentwise criterion for statistical significance it was found that upwind emissions and concentrations were significantly related (p < 0.05). However, correlation's were sensitive to site location, time upwind of the emissions and season, and ranged from −0.03 to 0.50. Correlations were weaker at sites located west of the high emission region in the midwestern U.S.A. and stronger at sites further away and to the east of this region. There was a decrease in the strength of the correlations from the warm season to the cold season. It was also found that differences in meteorology between events obscured the relationship between emissions and concentrations. The effects of variations in ambient temperature and precipitation amount on wet SO₄²⁻ concentrations were taken into account by calculating partial correlation coefficients. A higher percentage of the resulting correlations were found to be statistically significant and the differences between sites decreased. This suggested that meteorological variability had a confounding influence on the detection of a link between concentrations and emissions. This influence should be considered when studying source-receptor relationships.     

Biogenic and anthropogenic organic compounds in eolian particulates in the East Mediterranean region—I. Occurrence and origin

Lipids of biogenic and anthropogenic origin were determined in aerosol samples, collected seasonally, in a coastal area on the north of the island of Crete. Lipid classes such as n-alkanes, hopanes, polycyclic aromatic hydrocarbons, fatty alcohols, fatty acids, fatty acid salts and α,ω-dicarboxylic acids were characterized by GC/MS and GC/FID analysis, in terms of their contents of homologous compound series. The concentrations ranged between 56 and 215 ng m⁻³ for n-alkanes, 10 and 52 ng m⁻³ for polycyclic aromatic hydrocarbons, 2 and 31 ng m⁻³ for fatty alcohols, 13 and 279 ng m⁻³ for fatty acids, 24 and 220 ng m⁻³ for fatty acid salts and 0.4 and 7.5 ng m⁻³ for α, ω-dicarboxylic acid salts. The prevailing winds were influencing the composition of the eolian particles. Generally, aerosols sampled during south wind events predominantly contained lipids originating from higher plants, while when north and northwest winds prevailed the major components were of marine origin. The absence of unsaturated fatty acids in all aerosol samples is related to the presence of α,ω-dicarboxylic acids, which are believed to be their photo-oxidation products.