NASA's Satellite Laser Ranging Systems for the 21st Century.

For over 40 years, NASA's global network of satellite laser ranging (SLR) stations has provided a significant percentage of the global orbital data used to define the International Terrestrial Reference Frame (ITRF). The current NASA legacy network is reaching its end-of-life and a new generation of systems must be ready to take its place. Scientific demands of sub-millimeter precision ranging and the ever-increasing number of tracking targets give aggressive performance requirements to this new generation of systems. Using lessons learned from the legacy systems and the successful development of a prototype station, a new network of SLR stations, called the Space Geodesy Satellite Laser Ranging (SGSLR) systems, is being developed. These will be the state-of-the-art SLR component of NASA's Space Geodesy Project (SGP). Each of SGSLR's nine subsystems has been designed to produce a robust, kilohertz laser ranging system with 24/7 operational capability and with minimal human intervention. SGSLR's data must support the aggressive goals of the Global Geodetic Observing System (GGOS), which are 1 millimeter (mm) position accuracy and 0.1 mm per year stability of the ITRF. This paper will describe the major requirements and accompanying design of the new SGSLR systems, how the systems will be tested, and the expected system performance.

MoSearch: a radiologist-friendly tool for finding-based diagnostic report and image retrieval.

The diagnostic reports generated in a radiology department contain a wealth of information. Although radiology information systems can greatly facilitate patient-based access to this information, they typically provide only limited finding-based access. A user-friendly personal computer-based software package that allows radiologists to conduct sophisticated real-time searches of diagnostic reports on the basis of patient characteristics, modality used, anatomy examined, and imaging findings and to easily review, refine, and output the results was designed and implemented in a large academic hospital. A notable feature of this system is the use of synonym-matching and syntactic cues, which allow it to identify findings within the text of a diagnostic report much more accurately than a simple keyword search can. This type of system is easily and inexpensively implemented and is a valuable tool in the support of various research and teaching applications in a radiology department.

Feed associated haemorrhagic disorder in pigs accompanied by pancreatic lesions.

The introduction of a new batch of feed to 400 pigs aged five to eight weeks resulted in 38 deaths and further morbidity associated with multiple haemorrhages. Signs abated within two days of withdrawal of the feed. Widespread haemorrhages were present in many tissues including the pancreas. Additional pancreatic lesions comprised focal necrosis, atrophy and fibrosis of exocrine tissue. The condition was reproduced experimentally in pigs and vitamin K protected mice against the injurious effects of the feed. The cause was not determined but it is speculated that more than one toxic factor and an imbalance of nutritional factors may have been present in the diet.

Chemical composition of the spinal cord in the normal developing fetus and in the premature foal.

The lipid content of spinal cord, expressed as a percentage of adult values, was considerably higher for newborn foals than for several other species and traces of esterified cholesterol (type A) were only rarely present in horse fetal cord (from 270 days gestational age onwards). This suggested that, at birth, the spinal cord is neurochemically more 'mature' in the horse than in cattle, sheep and pigs. Data for premature foals revealed no lipid abnormality suggestive of myelin immaturity or degeneration.

Verruculogen Produced by soil fungi in England and Wales.

Soil fungi, including Aspergillus fischeri, Penicillium piceum, Penicillium nigricans, and Penicillium raistrickii, produced a tremorgenic toxin previously described as toxin X. Chemical analysis showed that this toxin was predominantly verruculogen.

Effect on calves of barley naturally contaminated with ochratoxin A and groundnut meal contaminated with low concentrations of aflatoxin B1.

Four groups of six 12-week-old male Friesian calves were fed diets containing 390 to 540 microgram ochratoxin A per kg, 320 to 500 microgram ochratoxin A plus 12 to 13 microgram aflatoxin B1 per kg, 10 to 13 microgram aflatoxin B1 per kg, or a control diet containing neither toxin. At the end of the 87-day experiment there was no evidence of kidney or liver damage in any group of animals as judged by serial plasma and urine enzyme assays, haematological examinations including the assay of blood coagulation factors, gross appearance at autopsy or histopathological assessment at the light microscopic level. Nor was there any significant alteration in serum IgA, IgM, IgG1 and IgG2 levels or in titres to environmental bacterial and viral antigens. Trace amounts of ochratoxin A were detected in kidneys of five out of the 12 calves exposed to this toxin but all 12 kidneys contained residues of the metabolite ochratoxin alpha (less than 5 to 10 microgram/kg). Traces of aflatoxin B1 and M1 were detected in the liver of one of the 12 calves exposed to aflatoxin B1 but nine kidneys contained the metabolite aflatoxin M1 (less than 0.01 to 0.03 microgram/kg). There was no evidence of interaction between the two toxins.

Rapid, economical method for determination of aflatoxin and ochratoxin in animal feedstuffs.

A quantitative procedure widely used in European Economic Community (EEC) countries has been successfully scaled down to produce a rapid method for determination of aflatoxin B1 (and other aflatoxins) in animal feeds. Without modification, the method may be used for simultaneous ochratoxin A determination in simple feeds, but a slightly different extraction procedure is required for compound feeds. Validity of the method has been demonstrated by comparison with the full EEC procedure for aflatoxin B1 and the Nesheim method for ochratoxin A. Analyses may be completed within 2 h and there is a considerable savings in materials over the 2 reference methods. The procedure is also less hazardous because volumes of toxic extract are small, and the operator is exposed to minimum solvent vapor.

Changes in plasma enzyme activities and other blood components in response to acute and chronic liver damage in cattle.

Three calves were dosed orally with carbon tetrachloride at 0.05, 0.1 or 0.3 ml/kg body-weight. Plasma enzyme activities, clotting times, bilirubin concentrations and bromsulphthalein elimination times increased. These changes are associated with damage to the liver and are discussed in relation to the clinical syndrome. Three groups of seven calves were infected weekly with 10, 50 or 100 Fasciola hepatica metacercariae for 12 consecutive weeks. Maximum glutamate dehydrogenase and gamma glutamyltransferase activities in the plasma were greater with the larger infecting doses but there was no change in plasma clotting times.

Aflatoxin B1 in dairy concentrates and other animal feedstuffs.

Over a period of 13 years 740 samples of various animal feedstuffs were analysed for the presence of aflatoxin B1. Nearly 500 were suspected of causing disease in farm animals but aflatoxin B1 could be detected in only 13.6 per cent of them. Groundnut meal samples nearly always contained the toxin but compounded feeds were contaminated to a varying extent. In particular, none could be detected in 62 poultry feeds. Where mycotoxicosis was suspected in dairy cattle, aflatoxin B1 was present at levels of more than 30 micrograms per kg in about 27 per cent of associated feed samples. In other dairy feeds (178 samples) this level of contamination was present in only about 9 per cent of samples. Concentrations of aflatoxin B1 likely to produce toxic effects (100 micrograms per kg and above) were present in about 4 per cent of suspect dairy concentrates but in 1 per cent or less of others. Contamination of dairy concentrates with aflatoxin B1 is usually at such a level that cows probably excrete the toxic metabolite aflatoxin M1 in milk at very low concentrations of 0.1 micrograms per litre or less.

Bovine virus diarrhoea-mucosal disease virus: pathogenicity for the fetal calf following maternal infection.

Fifteen pregnant, bovine virus diarrhoea-mucosal disease (BVD-MD) antibody-free Jersey heifers were infected experimentally with a mixture of 10 cytopathic strains of BVD-MD virus isolated from cattle in Britain. Each cow was inoculated intramuscularly on gestation day 100 with a high or a low dose of virus grown in primary calf testis tissue cultures. None of the cows showed clinical signs of illness following exposure, but all had seroconverted within six weeks. Six fetuses, including one set of twins, died in utero following infection. Of these five were aborted between days 136 and 154; the sixth one was mummified and still retained at day 300. The remaining 10 fetuses survived to term, but all showed evidence of intrauterine growth retardation with or without gross malformation and/or dysmyelination of the central nervous system. Three were clinically affected with congenital nervous disease. Of the 10 liveborn fetuses, two had specific serum antibodies to BVD-MD. Non-cytopathic BVD-MD virus was recovered from all of the remaining eight. When non-immune cows become infected with BVD-MD virus in mid gestation: transplacental infection of the fetus will probably result; apart from the risk of fetal death, with or without abortion, there is a high probability of fetal mal-development which may not always be clinically obvious; the immunological competence of the fetus may be impaired; congenital infection is likely in a substantial proportion of liveborn calves. About one in 16 bovine fetuses in British herds are estimated to be at risk from BVD-MD virus infection.

Mycotoxins in animal feedstuffs: sensitive thin layer chromatographic detection of aflatoxin, ochratoxin A, sterigmatocystin, zearalenone, and T-2 toxin.

Improvements have been made to a previously described multi-mycotoxin method that involved a membrane cleanup step. Using 2-dimensional thin layer chromatography and appropriate solvent systems, aflatoxin B1 can be detected in mixed feedstuffs and various ingredients at levels ranging from 0.1 to 0.3 microgram/kg. Corresponding detection limits for ochratoxin A and sterigmatocystin are 5 to 20 microgram/kg and for T-2 toxin and zearalenone 20 to 200 microgram/kg.