Pulsed underwater corona discharges as a source of strong oxidants: *OH and H2O2.

Because of undesirable side effects of chemical methods pulsed underwater corona discharges are emerging as a potential future advanced oxidation process (AOP) for water disinfection. In pulsed corona discharges a discharge channel is created, which contains a non-thermal plasma with a low degree of ionisation and low electron densities, but with electron energies of up to 10 eV. It has been demonstrated that electrons with this energy can dissociate water and oxygen molecules and produce various reactive radicals (*OH, H*, O*, HO2*), molecular species (H2O2, H2, O2), ultraviolet radiation and shock waves. It is supposed that the combination of all effects leads to a very efficient killing of microorganisms. To understand this in detail and to improve the efficiency of the overall system there is the need to develop suitable diagnostic methods for the quantitative determination of the various oxidants produced during the discharge. In this paper we present preliminary experimental results obtained with different chemical probes for *OH radicals, and H2O2 produced by pulsed corona discharges.     

Intensive computer keyboard training programmes

An intensive computer keyboard training course, based on an information processing model of man, was tested on a variety of personnel in work. Over a one or two week period, 241 adult subjects were trained. Subjects achieved mean speeds of 7.1 words per minute (WPM) after the second and 13.7 WPM after the ninth lesson. Significant decreases in errors per minute (EPM) occurred from 2.67 to 1.78. Previous experience with a keyboard and being female were factors associated with enhanced keyboard operating performance. Compressing the ten lessons from two into one week reduced the effectiveness of the programme.     

Multiplex polymerase chain reaction assay for the differential detection of trichothecene- and fumonisin-producing species of Fusarium in cornmeal

The genus Fusarium comprises a diverse group of fungi including several species that produce mycotoxins in food commodities. In this study, a multiplex polymerase chain reaction (PCR) assay was developed for the group-specific detection of fumonisin-producing and trichothecene-producing species of Fusarium. Primers for genus-level recognition of Fusarium spp. were designed from the internal transcribed spacer regions (ITS1 and ITS2) of rDNA. Primers for group-specific detection were designed from the TRI6 gene involved in trichothecene biosynthesis and the FUM5 gene involved in fumonisin biosynthesis. Primer specificity was determined by testing for cross-reactivity against purified genomic DNA from 43 fungal species representing 14 genera, including 9 Aspergillus spp., 9 Fusarium spp., and 10 Penicillium spp. With purified genomic DNA as a template, genus-specific recognition was observed at 10 pg per reaction; group-specific recognition occurred at 100 pg of template per reaction for the trichothecene producer Fusarium graminearum and at 1 ng of template per reaction for the fumonisin producer Fusarium verticillioides. For the application of the PCR assay, a protocol was developed to isolate fungal DNA from cornmeal. The detection of F. graminearum and its differentiation from F. verticillioides were accomplished prior to visible fungal growth at <10(5) CFU/g of cornmeal. This level of detection is comparable to those of other methods such as enzyme-linked immunosorbent assay, and the assay described here can be used in the food industry's effort to monitor quality and safety.     

Survey of current fracture mechanics studies at AMMRC

The fracture and fatigue studies at AMMRC encompass both experimental and analytical thrusts. This presentation will cover a few representative activities.

The status of a test program on fracture behavior of unidirectionally reinforced composites using double cantilevered type specimens will be reported. Material systems include ‘S’ glass/epoxy and graphite/epoxy. Limited fracture toughness data is available. Additionally, some effort has been initiated on cross ply specimens.

Fatigue studies at AMMRC in metals reflect a continuing interest in both initiation and propagation aspects. A technique has been developed for detection of crack initiation using an automated photographic process for recording, periodically, potential initiation sites. The observations are discussed in conjunction with damage criteria. Crack propagation studies have focussed in developing a ‘law’ which accounts for the extremes of propagation rates at threshold levels of stress intensity and at the higher levels associated with unstable growth. Additionally, crack propagation experiments are described which are aimed at exploring the transient effects on crack propagation of sudden changes in stress intensity levels.

Supplementing these experimental studies are extensive analytical efforts directed toward defining the stress states in anisotropic material when used in lap and/or mechanical joint configurations. Additionally, extensive effort by one team of investigators has been devoted to analytical techniques for crack analysis. These techniques have been applied to a wide variety of geometric configurations and to a range of material types including anisotropic. This effort will be described briefly.     

Multiplex real-time PCR detection of fumonisin-producing and trichothecene-producing groups of Fusarium species

Some species of Fusarium can produce mycotoxins during food processing procedures that facilitate fungal growth, such as the malting of barley. The objectives of this study were to develop a 5' fluorogenic (Taqman) real-time PCR assay for group-specific detection of trichothecene- and fumonisin-producing Fusarium spp. and to identify Fusarium graminearum and Fusarium verticillioides in field-collected barley and corn samples. Primers and probes were designed from genes involved in mycotoxin biosynthesis (TRI6 and FUM1), and for a genus-specific internal positive control, primers and a probe were designed from Fusarium rDNA sequences. Real-time PCR conditions were optimized for amplification of the three products in a single reaction format. The specificity of the assay was confirmed by testing 9 Fusarium spp. and 33 non-Fusarium fungal species. With serial dilutions of purified genomic DNA from F. verticillioides, F. graminearum, or both as the template, the detection limit of the assay was 5 pg of genomic DNA per reaction. The three products were detectable over four orders of magnitude of template concentration (5 pg to 5 ng of genomic DNA per reaction); at 50 ng template per reaction, only the TRI6 and FUM1 PCR products were detected. Barley and corn samples were evaluated for the presence of Fusarium spp. with traditional microbiological methods and with the real-time PCR assay. The 20 barley samples and 1 corn sample that contained F. graminearum by traditional methods of analysis tested positive for the TRI6 and internal transcribed spacer (ITS) PCR products. The five corn samples that tested positive for F. verticillioides by traditional methods also were positive for the FUMI and ITS PCR products. These results indicate that the described multiplex real-time PCR assay provides sensitive and accurate differential detection of fumonisin- and trichothecene-producing groups of Fusarium spp. in complex matrices.