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Environmental air monitoring is of great interest due to the large number of people concerned and exposed to different possible risks. From the most common particles in our environment (e.g. by-products of combustion or pollens) to more specific and dangerous agents (e.g. pathogenic micro-organisms), there are a large range of particles that need to be controlled. In this article we propose an original study on the collection of electrostatically deposited particles using electrowetting droplet displacement. A variety of particles were studied, from synthetic particles (e.g. Polystyrene Latex (PSL) microsphere) to different classes of biological particle (proteins, bacterial spores and a viral simulant). Furthermore, we have compared ElectroWetting-On-Dielectric (EWOD) collecting efficiency using either a hydrophobic or a superhydrophobic counter electrode. We observe different cleaning efficiencies, depending on the hydrophobicity of the substrate (varying from 45% to 99%). Superhydrophobic surfaces show the best cleaning efficiency with water droplets for all investigated particles (MS2 bacteriophage, BG (Bacillus atrophaeus) spores, OA (ovalbumin) proteins, and PSL).

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A radiotracer method was applied to the measurement of inorganic contaminants migrating into food. The method was applied to the study of 10 samples of recycled paper and board. The only elements detected in the static migration test were zinc and iron, at concentrations close to the detection limit. Samples of rice, oats, custard powder, mushrooms and fries showed that traces of these elements had migrated from the packaging. The migration was limited to less than 1%, with the exception of the mushrooms, where the decomposition of the food had resulted in a 12.5% transfer of zinc from the mushroom bag after 8 days, equivalent to migration of 0.022 mg dm(-2). Shaking had no effect on migration, except in one case of custard powder where migration occurred at a level equivalent to 0.002 mg dm(-2). The maximum migration determined in the present study was 4.8 microg zinc and 2.6 microg iron, which is negligible when compared with the recommended daily intakes of 15 and 14 mg, respectively. When Tenax was tested as a food simulant, no zinc was detected (< 0.001 mg dm(-2)), although slight migration (0.001 mg dm(-2)) occurred into food.

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This study examines the feasibility of dual energy attenuation metering to measure the concentration of two elements in aqueous solution, in a pipe of fixed thickness. Photon energies between 20 and 30 keV were selected in order to be able to determine mg L(-1) metal concentrations. Pairs of elements from a group with atomic numbers between 24-82 (Cr, Cu, Zn, Hg and Pb) were used to test the methodology. The sensitivity of measurement for a mixture of two elements was predicted from the ratios of the attenuation coefficients at 20 keV to the ratios at 30 keV. Experimental results confirmed that the sensitivity was greatest for the mixture of Cr and Pb, since those elements have the largest ratio of attenuation coefficients (1.108) and it was possible to accurately analyse a solution containing 0.15 g L(-1) of Cr and 0.13 g L(-1) of Pb. Other pairs of elements with ratios at 1.074 and 1.078 (Cu/Pb, Cu/Hg,) could only be determined at g L(-1) concentrations. It was not possible to differentiate between the pairs of elements with attenuation coefficient ratios below 1.03 (Cr/Zn and Cr/Cu) in this study.

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The relationship of some dissolved trace metals (Al, Cr, Mn, Zn, and Pb) with one another and to dissolved phosphate and nitrate in a freshwater aquatic system at Flic en Flac and Grand River North West (GRNW) in Mauritius (1850 km2, 20 degrees S and 57 degrees E, Western Indian ocean) is reported following trace metal determination using inductively coupled plasma mass spectrometry (ICP-MS). Dissolved Al (<200 ng ml(-1)), Cr (<50 ng ml(-1)), Mn (<50 ng ml(-1)), Zn (< 100 ng ml(-1)), and Pb (<50 ng ml(-1)) upstream, downstream GRNW and in the marshes and rivulet at Flic en Flac were found to be below the recommended EEC maximum admissible concentrations and within the ambient drinking water quality standards in Mauritius. Dissolved Pb was significantly positively correlated to both dissolved Cr and Zn suggesting that the cycling for dissolved Pb is linked to the cycling of both dissolved Cr and Zn along GRNW. The common influential cycling of Pb and Zn was further reinforced as both dissolved Pb and Zn were significantly positively correlated to dissolved phosphate, which suggested a biological role in the cycling of Zn and Pb. The role of biological activity or adsorption to biological systems in Pb cycling along GRNW is further suggested as dissolved Pb was significantly correlated to dissolved nitrate. The apparent absence of the dissolved Al, Cr, and Mn with dissolved nitrate and phosphate could be attributed to factors such as the lower sensitivity of the GRNW to metal uptake during biological activity during the time frame considered. The cycling of dissolved Al and Mn was also not linked to the cycling of Cr, Zn, and Pb as no significant correlation was found along GRNW.

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The distribution of platinum, rhodium, and palladium (platinum-group elements; PGEs) adjacent to two major U.K. roads shows a rapid decrease (more than 1 order of magnitude) away from the road and reflects patterns shown by other traffic-derived trace elements such as Pb and Zn. However, ratios of Pt:Rh remain relatively constant from 0 to 10 m distance, suggesting that at least some of the PGEs are transported away from the source. A temporal study over a 12-month period, of road dust and surface samples, reveals elevated concentrations above background levels, with maximum values of Pt >500 ng g(-1), Rh 70 ng g(-1), and Pd 70 ng g(-1). Concentrations vary considerably throughout the year and show some tentative correlation with rainfall. Element speciation, an essential control on mobility and hence distribution, was investigated, and the results of solubility experiments show that up to 30% of the Pd present dissolves in acid solutions. This indicates that at least some of the Pd is present in a soluble form and is therefore potentially highly mobile.

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The spatial variability of soil pH for engineered Weathered Oxford Clay is described using 35 samples collected from the base of a new cell in an existing landfill. Soil pH variability influences the reactivity of Cr, Cu and Zn in the site. The reactivity of these metals as natural components was determined using a sequential extraction method. The total concentration of Cr, Cu and Zn and the mineralogical composition were also determined. The results showed that due to the presence of a layer rich in pyrite in the base, a natural acidification may occur which can produce a soil pH as low as 2.7. The spatial variability of soil pH in this area has been described with an anisotropical variogram model and the estimation of its values at unsampled locations was carried out using the ordinary kriging algorithm. From the spatial modelling of the soil pH, it was found that the metals in the soil solid phases follow a similar distribution.

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Chlorine is usually present at low concentrations in reactor materials and thermal neutron activation of (35)Cl produces (36)Cl, which has a long half-life and is a radionuclide of significance in nuclear waste disposal. This paper describes a radiochemical method that has been developed to measure low concentrations of Cl in reactor stainless steels, so that the amount of (36)Cl in radioactive wastes can be estimated. The method is based on the irradiation of a 1 g sample in a thermal neutron flux of 10(16) n m(-)(2) s(-)(1), followed by dissolution in HNO(3) with the addition of stable KCl carrier/tracer. The Cl is precipitated as AgCl, and the recovery is measured gravimetrically. The (38)Cl, which has a half-life of 37 min, is measured with γ-ray spectrometry. The entire process, from irradiation to the end of counting, takes ∼1.5 h. The recovery is near-quantitative, and the detection limit for Cl in most stainless steels is below 1 mg/kg.

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A new method has been developed to measure 129I in the environment with detection limits below 10 mBq/kg of vegetation and 10 mBq/l of cows' milk. The method is based on extraction of 129I from the milk or vegetation sample, onto an ion exchange resin. An inactive carrier of 127I is added to the sample before separation, to monitor losses throughout the entire procedure. The ion exchange resin is irradiated for 7.5 h in a neutron flux of 10(16) n m-2 s-1 to induce the 129I(n, gamma) 130I reaction with thermal neutrons. The 127I carrier undergoes a (n,2n) reaction with fast neutrons to produce 126I. Iodine is extracted from the ion exchange resin after irradiation with an elution scheme which removes contamination from the radionuclide 82Br, the main interference in the analysis. Finally iodine is precipitated as AgI for gamma ray analysis. The sample is counted for 3 h on a Ge semiconductor detector to measure the radionuclide 130I, which has a half life of 12.4 h and 126I, which has a half life of 13.0 days. The measured 130I activity is compared to a known standard to deduce the amount of 129I in the sample, and the concentrations are corrected for losses during processing using the measured activity of 126I. The detection limits for 129I by this method are below 10 mBq/l for milk samples and 10 mBq/kg for vegetation. In addition to routine monitoring of milk and grass samples the method has been used to measure 129I deposition on grass and soils in a field near the Sellafield plant. Results of these analyses, along with measurements of 129I in air and rainfall using the same methodology, have been used to determine deposition velocity and retention coefficients of 129I to grass.

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153Sm-DTPA provides a suitable alternative to 99mTc-DTPA and 111In-DTPA as a water soluble tracer for the evaluation of pharmaceutical preparations. The chelate was handled biologically in a similar way to 99mTc-DTPA and 111In-DTPA. The chelate can be incorporated into the formulation as a non-radioactive excipient and the intact dosage form can then be neutron activated to produce 153Sm.

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Both the parasympathetic and sympathoadrenal inputs to the pancreas can stimulate glucagon release and are activated during hypoglycemia. However, blockade of only one branch of the autonomic nervous system may not reduce hypoglycemia-induced glucagon secretion, because the unblocked neural input is sufficient to mediate the glucagon response, ie, the neural inputs are redundant. Therefore, to determine if parasympathetic and sympathoadrenal activation redundantly mediate increased glucagon secretion during hypoglycemia, insulin was administered to conscious rats pretreated with a muscarinic antagonist (methylatropine, n = 7), combined alpha- and beta-adrenergic receptor blockade (tolazoline + propranolol, n = 5) or adrenergic blockade + methylatropine (n = 7). Insulin administration produced similar hypoglycemia in control and antagonist-treated rats (25 to 32 mg/dL). In control rats (n = 9), plasma immunoreactive glucagon (IRG) increased from a baseline level of 125 +/- 11 to 1,102 +/- 102 pg/mL during hypoglycemia (delta IRG = +977 +/- 98 pg/mL, P < .0005). The plasma IRG response was not significantly altered either by methylatropine (delta IRG = +677 +/- 141 pg/mL) or by adrenergic blockade (delta IRG = +1,374 +/- 314 pg/mL). However, the IRG response to hypoglycemia was reduced to 25% of the control value by the combination of adrenergic blockade + methylatropine (delta IRG = +250 +/- 83 pg/mL, P < .01 v control rats). These results suggest that the plasma glucagon response to hypoglycemia in conscious rats is predominantly the result of autonomic neural activation, and is redundantly mediated by the parasympathetic and sympathoadrenal divisions of the autonomic nervous system.

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At the Imperial College Reactor Centre we have developed a fully automated, large sample, high sensitivity delayed neutron counting system for routine analysis of environmental samples and personnel monitoring. Two-hundred fifty samples with a maximum volume of 30 ml can be analysed each working day. The detection limits (3 sigma) for uranium of natural isotopic abundance in our routine samples are typically 1 microgram/kg (0.05 Bq/kg) for dry samples and 1 microgram/l (0.05 Bq/l) for aqueous samples. Daily analysis of BNFL uranium standards, 'in house' uranium standards and weekly analysis of IAEA Soil-7 reference material are used to ensure constant system sensitivity and accuracy.

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To investigate the neural regulation of pancreatic polypeptide (PP) secretion during hypoglycemia in the rat, insulin was administered to chronically cannulated rats, and plasma PP responses were compared between saline-treated animals and animals pretreated with a ganglionic blocking agent (hexamethonium), a muscarinic antagonist (atropine), combined alpha- and beta-adrenergic receptor blockade (propranolol + tolazoline), or combined adrenergic blockade + atropine. PP was measured using a new RIA which selectively detects PP in rat plasma. In control rats (n = 10), plasma PP increased from a baseline level of 30 +/- 3 pg/ml to 271 +/- 41 pg/ml during hypoglycemia (plasma glucose = 29 +/- 2 mg/dl) (delta PP = +241 +/- 42 pg/ml, P less than 0.0005), demonstrating that in rats, as in other species, insulin-induced hypoglycemia is a potent stimulus for PP release. PP only increased by 31 +/- 10 pg/ml during similar hypoglycemia in 7 hexamethonium-treated rats (P less than 0.01 vs. control animals). Thus, at least 90% of the PP response to hypoglycemia is neurally mediated. The plasma PP response to hypoglycemia was +85 +/- 24 pg/ml in atropine-treated rats (P 0.01 vs. control rats), suggesting that approximately 65% of the PP response is mediated via muscarinic acetylcholine receptors on the islet F cell. The PP response to hypoglycemia in rats with combined adrenergic blockade (delta = +168 +/- 32 pg/ml) was slightly, but not significantly smaller than that in control rats. The combination of combined blockade + atropine resulted in a PP response (delta = +26 +/- 7 pg/ml) to hypoglycemia that was similar to that in hexamethonium-treated rats (P less than 0.01 vs. control rats). These results suggest: 1) The PP response to hypoglycemia is predominantly the result of muscarinic, cholinergic activation. 2) There is a minor adrenergic contribution to the response. 3) The plasma PP response may be useful as an index of autonomic neural input to the islet during hypoglycemia.

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A radioimmunoassay for the measurement of rat pancreatic polypeptide (RPP) in serum or plasma has been developed and characterized using a new guinea-pig anti-rat-PP antibody. The assay provides a high degree of sensitivity and lacks cross-reactivity (CR less than 0.01%) to neuropeptide Y and peptide YY. It also does not interact with PPs of other species or peptide hormones namely, amylin, glucagon, human insulin, human-PP, human-proinsulin, rat C-peptide and rat insulin. The assay employs synthetic rat PP as standards from concentrations of 21-2100 pg/ml (i.e., 5-500 pM) and produces a sensitivity limit of 19 pg/ml (4.5 pM) PP at +/- 3 S.D. The intra- and interassay % coefficient of variations are 6.4% and 5.9%, respectively. The % recovery of RPP added to rat serum samples ranges from 98% to 103%. Assay of serum volumes ranging from 25 microliters to 100 microliters does not significantly alter the expected RPP level. The migration patterns of rat serum PP and that of a synthetic RPP are identical by Sephadex G-50 chromatographic analysis. The mean values of fasting and a 2 h post-feeding plasma RPP levels in normal rats are 40 +/- 2 and 80 +/- 10 pg/ml (9.5 pM and 19.0 pM), respectively. Rat-PP release during insulin induced hypoglycemia in conscious rats rises from 38 +/- 5 pg/ml to 261 +/- 34 pg/ml (9.0 to 62.1 pM, P less than 0.005) by 30 min. Additionally, the antibody used in this study cross-reacts well with mouse-PP as determined by linear serum dilution curves, thus making it useful in the measurement of murine-PP. In conclusion, we have developed and validated a sensitive and specific rat-PP assay. This assay provides a new tool for the reliable measurement of PP in physiologic studies using rat and mouse animal models.

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