The CLAS forward electromagnetic calorimeter

The CEBAF Large Acceptance Spectrometer (CLAS) at Jefferson Lab utilizes six iron-free superconducting coils to provide an approximately toroidal magnetic field. The six sectors are instrumented individually to form six independent spectrometers. The forward region (8°<θ<45°) of each sector is equipped with a lead–scintillator electromagnetic sampling calorimeter (EC), 16 radiation lengths thick, using a novel triangular geometry with stereo readout. With its good energy and position resolution, the EC is used to provide the primary electron trigger for CLAS. It is also used to reject pions, reconstruct π° and η decays and detect neutrons. This paper treats the design, construction and performance of the calorimeter.     

Responses of lactating Holstein cows to chilled drinking water in high ambient temperatures

In Experiment 1, 12 lactating Holstein cows were provided drinking water of either 10.6 or 27.0 degrees C for 24 h/d in a changeover design to examine the effects of water temperature on feed intake, water intake, respiration rate, rectal temperature, plasma thyroid hormone concentration, and milk yield. The 1st wk of each 3-wk treatment period was for adjustment and the next 2 wk were comparison periods. Least squares means for DM intake as a percentage of body weight were 3.68 and 3.57 for 10.6 and 27.0 degrees C treatment groups. Water intakes in liters per kilogram of dry feed consumed as a percentage of body weight were 21.3 and 20.3. Respiration rates were 70.5 and 81.0 breaths per minute; rectal temperatures were 39.7 and 39.9 degrees C, Triiodothyronine averaged .88 and .75 ng/ml; thyroxine, 42.4 and 39.2 ng/ml; cortisol, 3.03 and 2.06 ng/ml; and progesterone in milk, 4.58 and 3.15 ng/ml for the 10.6 and 27.0 degrees C treatment groups. Milk yield averaged 25.9 and 24.7 kg/d and FCM averaged 25.6 and 23.6 kg/d, respectively. In Experiment 2, 24 cows given a choice of chilled or warm water showed a clear preference (about 98%) for the warm water. If cows are given chilled water of 10 degrees C continuously, no warm drinking water should be available. Chilled drinking water lowered respiration rates and body temperatures and increased feed intake and milk yield.     

The analysis of dental acrylic polymers by pyrolysis-gas chromatography

The vast majority of polymers used in modern prosthetic dentistry are acrylic. They may be homopolymers or copolymers. A technique is described which involves the pyrolysis (thermal degradation) and subsequent analysis by gas chromatography of these polymers. Sample introduction is by means of a ferromagnetic wire which supports a film of the polymer obtained from a solution of the polymer in chloroform. Quantitative determinations can be achieved with the use of relevant standard copolymer compositions.     

Visualization of Large Experimental Space Using Holographic Mapping and Artificial Neural Networks. Benchmark Analysis of Multicomponent Catalysts for the Water Gas Shift Reaction

This paper reports the combination of Holographic Mapping (HM) and Artificial Neural Networks (ANNs) in order to provide a benchmark visualization of a multi-dimensional space in two-dimensional forms. In this approach each matrix point in HM represents virtual catalytic data generated by means of ANNs in order to visualize the given multi-dimensional experimental space. A 12-dimensional experimental space related to the composition of catalysts designed for the water gas shift reaction (WGSR) from 12 possible components supported on ZrO₂ is visualized. Catalytic data obtained in an earlier combinatorial screening process at 300 °C were used for training of the ANNs. The results show that the visualization of large experimental spaces having more than half a million virtual experimental points can be accomplished. The analysis of synergistic effects between different components revealed that the key components of water gas shift catalysts at 300 °C were Pt, Fe, Eu and V, while Co, Ru, Sb, Ge and Mo had a pronounced negative effect on the activity.     

Sourcing faecal pollution: a combination of library-dependent and library-independent methods to identify human faecal pollution in non-sewered catchments

Library-dependent (LD) (biochemical fingerprinting of Escherichia coli and enterococci) and library-independent (LI) (PCR detection of human-specific biomarkers) methods were used to detect human faecal pollution in three non-sewered catchments. In all, 550 E. coli isolates and 700 enterococci isolates were biochemically fingerprinted from 18 water samples and compared with metabolic fingerprint libraries of 4508 E. coli and 4833 enterococci isolates. E. coli fingerprints identified human unique biochemical phenotypes (BPTs) in nine out of 18 water samples; similarly, enterococci fingerprints identified human faecal pollution in 10 water samples. Seven samples were tested by PCR for the detection of biomarkers. Human-specific HF134 Bacteroides and enterococci surface protein (esp) biomarkers were detected in five samples. Four samples were also positive for HF183 Bacteroides biomarker. The combination of biomarkers detected human faecal pollution in six out of seven water samples. Of the seven samples analysed for both the indicators/markers, at least one indicator/marker was detected in every sample. Four of the seven PCR-positive samples were also positive for one of the human-specific E. coli or enterococci BPTs. The results indicated human faecal pollution in the studied sub-catchments after storm events. LD and LI methods used in this study complimented each other and provided additional information regarding the polluting sources when one method failed to detect human faecal pollution. Therefore, it is recommended that a combination of methods should be used to identify the source(s) of faecal pollution where possible.     

Direct application to dairy foods of a Listeria-specific oligonucleotide probe to 16S rRNA.

A potentially Listeria-specific 28 base oligonucleotide probe was designed from 16S rRNA sequence data. Using either 32P or non-radioactive (alkaline phosphatase) labels, the probe was shown to be highly specific as it hybridised to RNA extracted from all of the species of Listeria but not to any of the other bacteria tested. Both probe methods were highly sensitive and ca 10(2) cfu/ml Listeria could be detected in pure cultures. A rapid procedure for extracting RNA from milk, Camembert and cottage cheese was developed. This allowed the direct application of the probe to these foods and gave a rapid and specific method of detecting > 10(2) cfu/g or ml Listeria in these foods.