The manual determination of ammonia in fresh waters using an ammonia-sensitive membrane-electrode

The use of a commercially-available ammonia-sensitive membrane-electrode for the manual determination of ammonia in discrete samples of fresh water has been investigated and the analytical procedure is described. The electrode is simple and convenient to use, and a sample can be analyzed in a few minutes. For normal routine analysis, the lower limit of determination is approximately 0·1 mg N 1⁻¹ though smaller concentrations can be measured. The relative standard deviation of analytical results varied from approximately 10 to 3 per cent as ammonia concentration increased from 0·1 to 4 mg N 1⁻¹. Results for samples of river water agreed well with those obtained by absorptiometric methods of analysis; the electrode responds to amines but otherwise appears to be essentially specific for ammonia. Use of the electrode will be advantageous in a number of applications, and it also has good potential for the on-line analysis of fresh waters.     

Assessment of environmental tobacco smoke exposure: urinary cotinine concentrations in children are strongly associated with the house dust concentrations of nicotine at home

In the present study the possibility of using nicotine in house dust as an index of environmental tobacco smoke (ETS) exposure was evaluated in an environmental investigation of 23 children with asthma. A standardized procedure for house dust sampling of nicotine with a filter holder connected to a vacuum cleaner, for a defined time and area was developed (F-nicotine). Also, house dust sampling was carried out from the vacuum cleaner bags of the homes (VC-nicotine). There was a larger variation in VC-nicotine (13-655, median 66 microg/g) compared with F-nicotine (15-393 median 156 microg/g). There were statistically significant associations between an inquiry data based ETS exposure index on the one hand, and urinary cotinine concentrations in children (U-cotinine), F-nicotine and VC-nicotine of their homes, on the other. The strong correlation between U-cotinine and F-nicotine (rs = 0.93; P < 0.0001) indicates that the new standardized house dust sampling method should be useful in ETS exposure assessment. However, further validation by a larger sample size with repeated measurements in the same homes is needed.     

Structural reliability software at the University of California, Berkeley

The paper provides an overview of three software for structural reliability analysis developed at the University of California, Berkeley. These are CalREL, which is a general-purpose structural reliability code written in FORTRAN; FERUM, which is a collection of Matlab^® files that can be used for structural reliability analysis in conjunction with simple finite element models; and OpenSees, which is an object-oriented code for nonlinear structural response simulation with reliability capabilities. Reliability analysis methods featured by these software include FORM, SORM, Monte Carlo simulation, and various importance sampling methods. In addition, variable importance and sensitivity measures are provided.     

Microbial activity and distribution during enhanced contaminant dissolution from a NAPL source zone

Laboratory experiments were conducted to assess microbial reductive dechlorination in one-dimensional sand columns containing a 10 cm long source zone of uniformly distributed residual tetrachloroethene (PCE) nonaqueous phase liquid (NAPL), a 10 cm long transition zone directly down-gradient of the source zone containing some nonuniformly distributed NAPL ganglia, and a 40 cm long plume region down-gradient of the transition zone. The activity and distribution of Sulfurospirillum multivorans, a PCE-to-1,2-cis-dichloroethene (cis-DCE) dechlorinating bacterium, was evaluated in columns containing either a mixed-NAPL (0.25 mol/mol PCE in hexadecane) or pure PCE-NAPL. Significant dechlorination of PCE to cis-DCE was observed in the mixed-NAPL column, resulting in 53% PCE-NAPL mass recovery in the effluent with PCE-NAPL dissolution enhanced by up to 13.6-fold (maximum) and 4.6-fold (cumulative) relative to abiotic dissolution. Quantitative real-time PCR targeting pceA, the PCE reductive dehalogenase gene of S. multivorans, revealed that S. multivorans cells were present in the NAPL source zone, and increased in numbers (i.e., grew) throughout the source and transition zones. In contrast, minimal reductive dechlorination and microbial growth were observed in the column containing pure PCE-NAPL, where aqueous-phase PCE concentrations reached saturation. These results demonstrate that microbial growth within NAPL source zones is possible, provided that contaminant concentrations remain below levels toxic to the dechlorinating organisms, and that microbial growth can result in significant bioenhanced NAPL dissolution.     

The acute effect of bunker C oil and an oil dispersant on: 1 Serum glucose, serum sodium and gill morphology in both freshwater and seawater acclimated rainbow trout (Salmo gairdneri)

Bunker C oil and an oil dispersant were tested for physiological stress on both freshwater and saltwater acclimated rainbow trout. Both compounds tended to reduce serum glucose levels with Bunker C causing the more significant decrease (P < 0.08), indicating a possible dysfunction of the kidney. The freshwater treatment group showed a significant decrease in sodium levels (P < 0.01) when treated with a dispersant, while under similar conditions, saltwater acclimated fish show a very marked increase in serum sodium concentrations (P < 0.025). Those fluctuations in sodium levels are resultant from direct interference with the energy activated sodium transport systems of the gills. Microphotographs of gill filaments and lamellae show severe damage caused by the dispersant and dispersant/oil mixture with less impairment resultant from Bunker C exposure.     

Organochlorine insecticides and PCB'S in sediments of Lake St. Claire (1970 and 1974) and Lake Erie (1971).

Sediments were collected on a grid from Lake St. Clair in 1970 and 1974 and from Lake Erie in 1971 and analysed for organochlorine insecticides and PCBs. Suspended solids were centrifuged from pumped water in the Detroit River in 1974. Residues of DDE, TDE and DDT were highest in sediment from the Western Basin (70.3 ppb) Lake Erie and lowest in sediment from Lake St. Clair (6.6 ppb in 1970 and 2.6 ppb in 1974). The Central and Eastern Basins of Lake Erie contained residues that fell about mid-way between these means. TDE was the predominant component of ΣDDT and was followed by DDE at approximately half this residue. While DDT represented the lowest component in lake sediments, it was the highest component in suspended solids from the Detroit River.HEOD was present in the entire lake system but at only a fraction of the level of ΣDDT. The mean residue in Lake St. Clair was only 0.1 ppb while Lake Erie sediments contained 1–2 ppb. The highest mean residue (3.6 ppb) was in suspended solids in the Detroit River. Other organochlorine insecticides were only occasionally identified.PCB residues in sediment were approximately 3 times higher than the total organochlorine insecticide residue, being highest in the Western Basin (252 ppb) and lowest in Lake St. Clair (19 ppb in 1970 and 10 ppb in 1974). The Detroit River and Central and Eastern Basins of Lake Erie had intermediate residues.Residues in Lake St. Clair indicated a decline in ΣDDT, HEOD, and PCB residues between 1970 and 1974, and this coincided with the restrictions on the materials. A core sample from the Western Basin of Lake Erie indicated that ΣDDT, HEOD and PCB began to accumulate in sediments in 1958, 1953, and 1956, respectively. This appeared to indicate a lag period of 2–5 years after wide-spread use occurred.     

Predictions of nitrate diffusion in sediment using horizontal attenuated total reflection (HATR) by Fourier transform infrared (FTIR) spectrometry

Using a novel and simple method based on horizontal attenuated total reflection (HATR) by Fourier transform infrared (FTIR) spectrometry, the effective diffusion coefficient, De, of nitrate in a contaminated anthropogenic sediment was estimated as 7.34 x 10(-6)cm2 s(-1). This method, which requires as little as 1 mL of sediment sample, was able to measure the De of a chemical species with a reproducibility of +/-3% in about 5h. Based on this De and a pre-determined nitrate reduction rate, the profiles of nitrate concentration in two sediment columns were satisfactorily predicted from a mathematical model. Results showed that the profile in this aged sediment depended mainly on the diffusion of nitrate and, only to a much lesser degree, the rate of nitrate reduction. Measurements in 55 anthropogenic sediment samples collected from five locations and various depths of a contaminated site further showed that the De of nitrate increased linearly with the water content of the sediment, but decreased with the sediment density. The technique demonstrated in this study shall be applicable for the risk assessment of toxic pollutants in contaminated sediments, and for planning the spatial and time intervals of nitrate injection strategy in bioremediation.     

A new mathematical model to evaluate simazine removal in three different immobilized-biomass reactors

A new mathematical model based on the cinetical Langmuir equation is developed to interpret and predict the effectiveness of simazine (SZ) removal in immobilized-biomass reactor (IBR), to consider herbicide-support affinity (Cx), and herbicide-cell affinity (Cy). Three solid supports: sepiolite monolith, granular sepiolite, and alginate were used in pilot-scale reactors that were inoculated with Klebsiella planticola DSZ. The abiotic process was analysed by measuring the SZ sorption capacity of the reactor supports. Sepiolite monolith showed the maximum value for herbicide-support affinity (28.02+/-0.9%). The effectiveness of the biotic process was estimated considering the formation of biomass and SZ biodegradation. Granular sepiolite showed either higher affinity with SZ and viability rate (0.90) throughout the process, and SZ removal rate was 3.39+/-0.06 mg/h. The mathematical model presented in this paper provides useful insights into the interpretation of experimental data as well as prediction for the implementation of biological reactors.     

Speciation of selenium in plant water extracts by ion exchange chromatography-hydride generation atomic absorption spectrometry

Determination of selenium (Se) speciation in plants is important in studying the bioavailability and toxicity of Se in Se-contaminated soil/sediment. In this study, we used an anion exchange resin (Dowex 1-10X) to separate Se into non-amino acid organic Se, Se-amino acids, selenite (Se [IV]) and selenate (Se [VI]) in a plant (Stanleya pinnata) extract. The hydride generation atomic absorption spectrometry (HGAAS) was used to determine concentrations of these Se compounds in plant extracts. Results showed that Se compounds can be quantitatively separated by the resin column. Recovery of five spiked standard Se compounds (trimethylselenonium ion (TMSe+), dimethylselenoxide (DMSeO), selenomethionine (Semet), Se [IV] and Se [VII]) in the plant extract ranged from 92.9 to 103%. Water extractable Se accounted for 60.4-72.6% of the total Se in the plant. Among the soluble Se compounds in the plant extract, Se-amino acids were 73-85.5%, Se [VI] ranged from 7.5 to 19.5% and non-amino acid organic Se was less than 7%. Se [IV] in most samples was below the detection limit (1 microg/g). This study showed that considerable amounts of the accumulated Se [VI] in the plant was metabolized to Se-amino acids during growth of the plant.     

Extreme wind speeds in mixed wind climates

In this paper, a technique is discussed which enables extreme wind speed probabilities in mixed wind climates to be determined. It is shown that in such wind climates the method is likely to yield more accurate probability estimates than the traditional Gumbel analysis of annual wind speed maxima, particularly for annual probabilities of less than 2% (i.e. return periods greater than 50 years). The technique requires a separate analysis of each significant wind-producing meteorological phenomenon and practical methods of achieving this are presented. Extreme wind speed parameters obtained from each analysis may then be combined to yield a “composite extreme wind speed diagram” and several examples illustrating this procedure are shown. By means of a numerical simulation of a typical mixed wind climate, a detailed study is made of the distribution of extreme wind gusts from different meteorological phenomena. This study indicates that a Gumbel analysis of 20 annual maxima may severely underestimate low annual probability (i.e. long return period) gust speeds.