Abstract Samples of four soils having a wide range of volume weights (0.65, 1.02, 1.25, 1.62 g/cm3) were either weighed or measured by volume and extracted with: (a) the Bray P1 extractant, (b) the Mehlich double acid extractant for P, K, Ca, Mg, Mn, Zn and (c) neutral N NH4OAc for K, Ca, Mg all at a soil/extracting solution ratio of 1:10. The soil test results were recorded on a volume basis in mg/dm3 and on a weight basis in mg/kg. The test values for all macronutrients obtained with all extractants decreased, relative to a constant volume, with increasing VW of soil when analyzed and expressed on a weight basis. Results based on the use of a volume sample (scooped) but calculated on an assumed weight of soil changed the values in direct ratio of 1/assumed VW. The use of an assumed VW has no justification, since uniform soil test results can be obtained when expressed on a volume basis by either using a scooped sample of known volume or a weighed sample followed by multiplication with the VW of each soil. 相似文献
The National Reference Laboratory for classical swine fever (CSF) virus in the Netherlands examined more than two million samples for CSF virus or serum antibody during the CSF epizootic of 1997–1998. The immense amount of samples and the prevalence of border disease (BD) virus and bovine viral diarrhoea (BVD) virus infections in Dutch pig herds necessitated the diagnostic efforts of the laboratory to be focused on generating CSF specific test results throughout the eradication campaign.
Detection of 82% of the 429 outbreaks was achieved through the combined use of a direct immunofluorescence and peroxidase assay (FAT/IPA) with samples (tonsils) collected from clinically-suspected pigs. This suggests that in the majority of the outbreaks, the pigs had clinical signs that were recognised by the farmer and/or veterinarians, indicating the presence of CSF virus in a pig herd. A positive diagnosis of 74% of all the tissue samples (tonsils) collected at infected pig holdings was established by FAT. More than 140,000 heparinised blood samples were examined by virus isolation, resulting in the detection of 4.5% of the infected herds. CSF virus was isolated in approximately 29% of all the blood samples collected from pigs at infected or suspected farms.
Several serological surveys — each done within a different framework — led to the detection of 13.5% of the total number of outbreaks. The detection of CSF virus antibody in serum was carried out by semi-automated blocking ELISA. Approximately 28.5% of the sera which reacted in the ELISA were classified as CSF virus-neutralising antibody positive and 26.5% as positive for other pestiviruses following the virus neutralisation test (VNT).
We concluded that two of the CSF laboratory diagnostic methods described were determinative in the eradication campaign: first, the FAT for the screening of diseased pigs; and second, the ELISA and VNT when millions of predominantly healthy pigs needed to be screened for the presence of CSF serum antibody. Decision-making on the basis of results generated by either method can, however, be seriously hindered when samples are examined from pig herds with a high prevalence of non-CSF pestiviruses. 相似文献
