Simple method for quantifying microbiologically assisted chloramine decay in drinking water

In a chloraminated drinking water distribution system, monochloramine decays due to chemical and microbiological reactions. For modeling and operational control purposes, it is necessary to know the relative contribution of each type of reaction, but there was no method to quantify these contributions separately. A simple method was developed to do so. It compares monochloramine decay rates of processed (0.2 microm filtered or microbiologically inhibited by adding 100 microg of silver/L as silver nitrate) and unprocessed samples under controlled temperature conditions. The term microbial decay factor (Fm) was defined and derived from this method, to characterize the relative contribution of microbiologically assisted monochloramine decay to the total monochloramine decay observed in bulk water. Fm is the ratio between microbiologically assisted monochloramine decay and chemical decay of a given water sample measured at 20 degrees C. One possible use of the method is illustrated, where a service reservoir's bulk and inlet waters were sampled twice and analyzed for both the traditional indicators and the microbial decay factor. The microbial decay factor values alone indicated that more microbiologically assisted monochloramine decay was occurring in one bulk water than the other. In contrast, traditional nitrification indicators failed to show any difference. Further analysis showed that the microbial decay factor is more sensitive and that it alone can provide an early warning.     

Locating and quantifying PCB sources in Chicago: receptor modeling and field sampling

Potential source contribution function (PSCF) modeling using polychlorinated biphenyl (PCB) concentrations measured in the Chicago area resolved three PCB source sectors. They were (i) the direction northwest of Chicago, (ii) the direction southwest of Chicago, and (iii) the south side of Chicago in the neighborhood of Lake Calumet. The area south of Chicago was further examined by taking upwind/ downwind samples near a landfill and sludge drying beds. Results identified the sludge drying beds and a large landfill as PCB sources to the atmosphere. Another PCB source identified in Chicago was a transformer storage yard. This site had the highest upwind/downwind concentration increments in this study (downwind PCB concentrations were more than 5 times those in the upwind air). These PCB sources were characterized in terms of inventories, emission rates, contributions, and PCB congener profiles (fingerprints). Preliminarily results indicate that the sludge may emit up to 90 kg/yr of PCBs to the air. This amount is probably not a significant contribution of PCBs to the Chicago atmosphere on the basis of dispersion modeling results and a simple box model.     

The intravenous halothane test as an experimental method for quantifying stress sensitivity in pigs

The venous blood pH, pCO₂, lactate, pyruvate and haematocrit responses to an intravenous (i/v) infusion of halothane-lipid emulsion were assessed in Pietrain, Pietrain X Norwegian Landrace and Gloucester pigs. Halothane-induced lactacidosis was dose related in the Pietrain (stress sensitive) pigs between 0 and 82 μl halothane kg^?-1, whereas the crossbred and Gloucester pigs did not show any lactacidosis. It is concluded that the i/v halothane test can be used to quantify a stress sensitive pig's reaction to the drug, and that the crossbred pig does not express halothane sensitivity even at a mild level. Carazolol pretreatment in Pietrain pigs increased the halothane-induced lactacidosis, whereas in a separate study carazolol was found to decrease their rate of post-mortem muscle acidification. This indicates that halothane activates a different mechanism from stress when inducing lactacidosis in stress sensitive pigs.     

Field validation of a milk-line sampling device for monitoring milk component data

The objective of this study was to investigate the ability of a milk-line sampling device to obtain a representative sample under field conditions by comparing the milk component composition between milk-line and bulk-tank samples, for milk harvested from the same group of cows at the same milking. A total of 42 paired milk-line and bulk-tank samples were collected at separate milking events from 21 different dairy herds. Samples were analyzed for milk fat (%), true protein (%), and milk urea nitrogen (mg/dl). Concordance correlation coefficients showed a very high level of agreement between the two sample types, with values ranging between 0.82 and 0.95 for the components measured. ANOVA showed that milk component data derived from milk-line samples were neither statistically nor numerically different from milk component data derived from bulk-tank samples. The strategy of monitoring milk component data through milk line sampling should provide dairy producers with inexpensive, timely, and accurate information that will help to improve ongoing nutritional monitoring programs for individual groups of cows within the dairy herd.     

Development of QuEChERS-based extraction and liquid chromatography-tandem mass spectrometry method for quantifying flumethasone residues in beef muscle

A rapid, specific, and sensitive method based on liquid chromatography-electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) in the positive ion mode using multiple reaction monitoring (MRM) was developed and validated to quantify flumethasone residues in beef muscle. Methods were compared between the original as well as the EN quick, easy, cheap, effective, rugged, and safe (QuEChERS)-based extraction. Good linearity was achieved at concentration levels of 5-30μg/kg. Estimated recovery rates at spiking levels of 5 and 10μg/kg ranged from 72.1 to 84.6%, with relative standard deviations (RSDs)<7%. The results of the inter-day study, which was performed by fortifying beef muscle samples (n=18) on 3 separate days, showed an accuracy of 93.4-94.4%. The precision (expressed as relative standard deviation values) for the inter-day variation at two levels of fortification (10 and 20μg/kg) was 1.9-5.2%. The limit of detection (LOD) and limit of quantitation (LOQ) were 1.7 and 5μg/kg, at signal-to-noise ratios (S/Ns) of 3 and 10, respectively. The method was successfully applied to analyze real samples obtained from large markets throughout the Korean Peninsula. The method proved to be sensitive and reliable and, thus, rendered an appropriate means for residue analysis studies.     

污染场地土壤环境初步调查采样方法研究

为了保护生态环境,节约土地资源,本文以工业用地为例进行土壤环境初调,以期了解当地土壤污染程度、污染类型与分布情况,在采样布点时应注意点位确定与深度选取,并结合区域实际情况制定采样方案、科学布设采样点,使污染区的土壤环境得到有效改善,为生态环保工作贡献更多力量.     

An exploratory observational study to develop an improved method for quantifying beef carcass salable meat yield

Eighty-seven grain-finished steers were harvested, evaluated, and fabricated into wholesale cuts to determine what measured composition indicators most accurately describe the percentage of closely trimmed salable meat yield. Indicators of lean and fat composition present at the cross-section between the 12th and 13th ribs were objectively evaluated using Assess image analysis software. Salable meat yield ranged from 50.18% to 72.92%, trimmable fat yield ranged from 12.87% to 36.69%, and bone yield ranged from 10.07% to 19.21%. Regression models were developed to estimate percentage of total salable meat yield. Composition indicators chosen to predict salable meat yield included hot carcass weight (HCW), perinephric fat weight, longissimus muscle area (LMA), subcutaneous fat thickness (SFT), ratio of LMA to subcutaneous fat area, and ratio of subcutaneous fat depth to HCW. These results indicate that prediction of beef carcass salable meat yield can be improved via modification to current measures used in the USDA yield grade equation and addition of new measures.     

Field evaluation of mechanical milk sampling devices on road tankers

Six tanker-mounted milk sampling devices (called 'samplers') were evaluated by comparing the samples taken by them with those taken manually from the same milk supplies by trained operators. The samplers under test, although of different design, transferred the milk from the tanker milk line directly to the sample bottle at a point near the milk pump. The sampling rate was adjusted before each operation to ensure a fixed sampling rate from the complete supply and provide a standard sample size. When sampling for compositional quality (per cent fat) from refrigerated farm bulk milk tanks the mean difference (bias) between sampler and manual control values ranged from 0.003 to 0.018, while the standard deviation of individual differences (sampler - control) ranged from 0.043 to 0.088. When sampling for hygienic quality the mean difference (bias) between sampler and control samples for the standard plate count (expressed as log₁₀) ranged from 0.026 to 0.39, while the SD of individual differences ranged from 0.11 to 0.49.
It is concluded that with correct installation and operation the sampling devices tested are satisfactory for sampling producer milk supplies for compositional quality but not all are suited for sampling for hygienic quality. However, with minor adjustment in design or operation, in some cases performance may be improved.     

New device and method for flux-proportional sampling of mobile solutes in soil and groundwater

The importance of monitoring the transport of organic contaminants in soil and groundwater, and the pros and cons of existing sampling methods, are outlined. A new, alternative sampling method is proposed, using a passive sampler that functions as a water-permeable, semi-infinite sink for passing solutes of interest. Tracers integrated in the device store information on the volume of water passing through the sampler during the installation period. The conceptual basis of the sampling method is described. This device enables flux-proportional monitoring of the concentrations of mobile contaminants in the soil and groundwater. 14C-labeled phenanthrene (PHEN) and glyphosate (GLY) are used as case study compounds in laboratory experiments. The sorption capacities and uptake kinetics of 13 adsorbents are screened and compared, as well as the dissolution kinetics of three tracer salts: calcium citrate, calcium fluoride (CaF2), and calcium hydrogen phosphate (CaHPO4). The application of the passive sampler is then demonstrated in long-term laboratory experiments, using large soil columns under steady-state hydraulic conditions. The accumulated flux of PHEN was sampled with an accuracy of 3.6%-17.8%, using graphitized carbon, hexagonal mesoporous silica, and cross-linked polymers as adsorbents. The accumulated flux of GLY was sampled with an accuracy of 12.4%, using gamma-alumina as an adsorbent. The advantages and limitations of this new environmental monitoring method are discussed.     

横机编织系统生产效率的预测

工作效率评估是藉由统计和随机观察方法,找出某一项工作不同工序的百分比值。评估结果通常用于两部门工作效率、工作量分配和有效处理时间的合理安排,并对无效率工作做出解释。采用工作抽查法,观测和计算出横机设备利用率与生产时间的比值,确定了不同工序在两种不同组织结构中所占有的份额。本项研究分别在两种不同的电子控制横机上完成。     

Field validation of a milk line sampling device for monitoring milk quality and udder health

The objective of this study was to investigate the ability of a milk line sampling device to obtain a representative sample by comparing SCC and bacterial culture results between milk line and bulk tank samples for milk harvested from the same group of cows at the same milking. A total of 42 paired milk line and bulk tank samples were collected at separate milking events from 21 different herds. Concordance correlation coefficients showed a high level of agreement between the two sample types, with values ranging between 0.74 and 0.99 for all parameters and bacterial species measured. ANOVA showed that SCC and bacterial culture results for Streptococcus agalactiae, Staphylococcus aureus, Streptococcus non-agalactiae, Coliforms, and coagulase-negative staphylococci were neither numerically or statistically different between milk line and bulk tank samples. KAPPA analysis showed that overall agreement beyond chance between milk line and bulk tank samples in determining whether a herd was positive or negative for either Strep. agalactiae or Staph. aureus were 100 and 75%, respectively. While further research is needed to fully assess the utility of this tool for the purpose of bacterial culture, the results of this study suggest that the strategy of milk line sampling is a very promising monitoring tool. This sampling strategy should provide producers with inexpensive and timely information that will help to improve programs for monitoring milk quality and udder health in commercial dairy herds.     

Rapid method for detection and detoxification of heavy metal ions in water environments using phytochelation

Phytochelatins (PCs, (gammaGlu-Cys)n-Gly (n = 2-11)) are produced by higher plants, algae, and some fungi in response to heavy metal ion exposure. A rapid and convenient method for quantifying heavy metal ion concentrations in water environments was developed using a chemically synthesized PC as a mediator. The chelating ability of the PC and quantification of the thiol group were utilized to measure heavy metal ions at low concentrations. The method requires only ten minutes for measurement and only 1 ml of a liquid sample. A range of homogeneous PCs (n = 4-7) were chemically synthesized using a peptide synthesizer. These, especially PC7, exhibited higher sensitivity and consistency of measurement than the native PC from Silene cucubalus, which produced a mixture of PC2, PC3, and PC4. Detoxification of heavy metal ions in vitro by PC was also investigated. Using the paper disc method, the cell growth inhibition zone caused by cadmium ion against Salmonella typhimurium TA1538 was significantly decreased by addition of PC. Furthermore, at the minimum inhibitory concentration of cadmium ion (200 microM) in a nutrient broth culture of S. typhimurium, cell growth was almost completely recovered by addition of PC to the medium.     

Passive sampling screening method using thin-layer chromatography plates

An in situ solid-phase extraction method, thin-layer chromatography (TLC) passive sampling, was investigated as a screening method for determining the presence of organic compounds in water using laboratory experiments and field applications. The TLC passive sampler developed in this research enables the spatial and temporal distributions of organic compounds to be determined qualitatively with little expense. The materials for the sampler developed here cost dollar 1.60 each. By first identifying the areas where a pollutant is present using the TLC passive sampling screening method, total analytical costs for monitoring programs may be reduced by eliminating unnecessary conventional analyses for locations where the pollutant is not present. Two organophosphorus pesticides, diazinon and chlorpyrifos, were used as a model for the development and as a potential application of the TLC passive sampling method. Passive sampler adsorption kinetics, enrichment factors, and extraction efficiencies were determined from batch experiments with exposure times ranging from 1 h to 4 weeks. In field applications, TLC passive sampling was conducted in natural and engineered systems with two silica gel extraction media, C2 and C18. Diazinon and chlorpyrifos were detected by analyzing the adsorbed compounds by high-performance liquid chromatography with ultraviolet detection.