Atomic absorption spectroscopic determination of lead extracted from acid-solubilized tissues.

A method is presented for determining lead in a variety of tissues. Lyophilized samples are solubilized with nitric acid at room temperature in glass screw-cap culture tubes. Following neutralization with sodium hydroxide and sodium bicarbonate, the lead is extracted into methyl isobutyl ketone as the pyrrolidine dithiocarbamate complex and analyzed by flame atomic absorption spectrophotometry. Brain, heart, liver, lung, and spleen gave recoveries ranging from 92 to 102% with standard deviations of less than 8%. Aorta, kidney, and rib were unsuitable for analysis by this method. A large number of samples can be analyzed without specialized equipment or intricate experimental steps. The detection limit is 35 ng/g tissue (wet weight) and sensitivity is approximately 140 ng/g tissue (wet weight).     

Gas-liquid chromatographic determination of kepone residues in finfish, shellfish, and crustaceans.

Finfish, shellfish, and crustacean samples are extracted with isopropanol and benzene; the extract is filtered and then concentrated. The extract, dissolved in hexane, is treated with oleum and extracted with aqueous alkali. The aqueous phase is acidified and extracted with petroleum ether-ethyl ether (1 + 1). The Kepone residue is determined by electron capture gas-liquid chromatography (GLC). Recoveries obtained by 8 laboratories from 15 species of finfish fortified at 0.02-0.23 ppm ranged from 37 to 107% with a mean +/- relative standard deviation of 79.4 +/- 14.5%. For oysters fortified at 0.01-0.10 ppm, recoveries range from 63 to 129% with a mean of 78.8 +/- 20.8%. For crustaceans fortified at 0.05-0.26 ppm, recoveries ranged from 52 to 110% with a mean of 78 +/- 16.4%. The approximate limits of quantitation for finfish and for shellfish and crustaceans are 0.02 and 0.05 ppm, respectively, under the GLC conditions used in this study.     

Microbiological method for assaying lincomycin in animal feed: collaborative study.

A microbiological assay for determining lincomycin in swine feed, supplement, and a vitamin-mineral premix was studied collaboratively in 16 laboratories. The design of the study involved a complete feed, feed supplement, and a vitamin-mineral premix covering a range of fortification from 20 to 80 g/ton and 80 to 2600 g/ton. Two methods of sample preparation were used depending on the concentration of lincomycin in the sample. Statistical evaluation of the results from the 2 methods indicated that 10 and 11 collaborators, respectively, had mean recoveries which were not significantly different from one another. Ten laboratories obtained a mean recovery of 112.2% (range 102.3--123.5%) for the lower level, and 11 laboratories obtained a mean recovery of 104.4% (range 100.0--107.7%) for the higher level. The method has been adopted as official first action.     

Semiautomated method for determining ferrous sulfate in pharmaceuticals: collaborative study

A semiautomated colorimetric method is described for determining ferrous sulfate in tablets, capsules, and elixirs. The method involves the formation of an orange-red complex between 1,10-phenanthroline and ferrous ion. Collaborators were supplied with 3 solid composites and one liquid sample. Two of the solid composites were prepared from commerical tablets of different dosage and one from commercial timed-release capsules; the fourth sample was an elixir. The results of the automated analyses for ferrous sulfate agreed well with those of the applicable USP method. No interference was found from ferric iron or from the red and green coloring used on coated tablets. The method has been adopted as official first action.     

The response of cylindrocladium conidia to soil fungistasis

Direct observation of washed conidia of Cylindrocladium scoparium on non-sterile soils, air dried and rewetted immediately before deposition of conidia, indicated that peak germination (33–58%) occurred after 24 h incubation at 26°C. Peak germination on continually moist soils was lower (18–26%) than on rewetted soils. Lysis of germ tubes and germinating conidia on continually moist soils at 26°C was evident with 48 h. Conidia did not germinate on continually moist soils at 6°C and lysis did not become apparent until 168 h. Conidia germinated at a high level (93–99%) in axenic culture in the absence of exogenous C and N sources. The inhibition of conidial germination on soils may be attributed, in part, to the presence of soil volatiles. Germination of conidia placed on washed agar disks and exposed to volatiles from four soils ranged from 51 to 86% of the no-soil controls. Addition of carbon (13 ng C per conidium as glucose) and nitrogen (65 pg N ng^?1 C as NH₄C1) nullified the inhibitory effect of the soil volatiles. Germinability assayed on a selective medium at 26°C of conidia in artificially infested soils (approximately 10⁴ conidia g^?1 soil) decreased progressively during incubation at 26°C from 1 week to 4 months. No germinable conidia were recovered from artificially infested soils after 2 months incubation at 6°C. Conidia of C. floridanum and C. crotalariae responded similarly to C. scoparium in many assays.     

Microbial populations in pullman clay loam receiving large applications of cattle feedlot waste

One way to disperse waste from large commercial feedlots is to spread large amounts of the waste on limited areas nearby. The effects of this practice on the soil microbial populations was assessed. Feedlot waste (FLW) was applied for 5 yr at rates of 0, 22, 67, 134, and 269 t ha^?1 yr^?1. Additional treatments were 538 t ha^?1 yr^?1 for 1 and 3 years and applications of N and NPK fertilizer. Soil cores from plots were sampled for microbial analysis before, during, and after the fifth growing season. April, July. and December soil samples were analyzed to 180-, 20-, and 480-cm depths, respectively. The following utritional and physiological groups of microorganisms were counted: soil fungi on Rose Bengal agar; bacteria on a basal mineral salts medium, on nutrient agar (both aerobically and in BBL GasPak jars), and on EMB agar (Escherichia coli-type colonies and total counts); and nitrifying and denitrifying organisms. Little effect due to FLW application rates was found, and organisms producing coliform-type colonies on EMB agar did not persist in the soil. The results indicated that applying large amounts of feedlot waste will not deleteriously affect soil microorganisms.     

Interactions between Escherichia coli and allophane—I. Adsorption

Sorptive interactions between Escherichia coli (ATCC 11303B) and a purified allophane clay fraction were studied quantitatively using electronic particle counting and electrophoresis. Adsorption was influenced by pH and ions present at the allophane surface. These effects could be rationalized by considering changes in the net surface charge of the components. Electronic particle counting studies at pH 5.5 and above gave adsorption isotherms that obeyed single-term Langmuir kinetics. At pH 4.5, a more complex two-step isotherm was obtained, which was attributed to aggregation of unadsorbed cells by Al solubilized from the allophane surface.     

The Prince Edward Islands: A sanctuary for seabirds in the Southern Ocean

This paper reviews the breeding distribution and numerical status of selected species of seabirds at 23 oceanic island groups in the Southern Ocean (between latitudes 35 and 70°S), based on census data and population estimates which have become available through increased scientific endeavour in the region during the last 15 years or so. The paper focuses on the avifauna of the Prince Edward islands, in the southern Indian Ocean, and points to the importance of these islands as a breeding station and sanctuary for seabirds. Only one oceanic island group, the Crozets, contains more species of breeding seabirds than the Prince Edward islands. Substantial segements (about 10% and greater) of the world breeding populations of the king and macaroni penguins, and the wandering, grey-headed, yellow-nosed and sooty albatrosses are based at the Prince Edward group. We recommend that Prince Edward Island (sensu stricto) should be a wilderness area, and that development at Marion Island should be kept to an absolute minimum.