Gas-liquid chromatographic analysis of ethephon and fenoprop residues in apples and their decline before and after harvest.

Ethephon (2-chloroethylphosphonic acid) and fenoprop (2-(2,4,5-trichlorophenoxy) propionic acid) may be determined in the same apple sample. After extraction with methanol, 2 separate methylation procedures were required to quantitatively convert each compound. Ethephon was esterified with diazomethane and analyzed by a flame photometric detector in the P-mode. Fenoprop was esterified with boron trifluoride/methanol and analyzed by electron capture gas chromatography. Average recoveries were about 95% at 0.05 ppm for both compounds. The limit of detection was 0.05 ppm for ethephon and 0.01 ppm for fenoprop in a 1 g sample. The persistence of both compounds before and after harvest was studied. Ethephon and fenoprop were applied simultaneously to apple trees at the recommended concentrations of 300 and 20 ppm, respectively. Ethephon residues averaged 1.6, 0.75, and 0.4 ppm at 2 hr, 10 days, and after washing at 13 days, respectively. The corresponding fenoprop residues were 0.70, 0.025, and 0.024 ppm.     

Decomposition of algal cells and components and their stabilization through complexing with model humic acid-type phenolic polymers

Axenic cultures of Anacystis, Microcoleus, Plectonema and Synechococcus isolated from Greenfield sandy loam and of Anabaena flos-aquae, Nostoc muscorum and Chlorella pyrenoidosa from other sources were cultured under light and constant aeration and with [U-¹⁴C]-glucose in the nutrient medium. Whole cells, cell walls, cytoplasm and extracellular polysaccharides of selected species readily decomposed in the soil and after 22 weeks between 61 and 81% of the added C had evolved as CO₂. Complexing of cell wall and cytoplasmic preparations from A. flos-aquae and N. muscorum with model humic acid-type phenolic polymers reduced decomposition of the cell walls by 40% and of the cytoplasm by 70%. Over 50% of the residual 14C activity in the soil amended with whole algal cells remained in the 0.5% NaOH-extracted soil. With exception of Microcoleus sp. more of the residual ¹⁴C from cell walls, cytoplasm and polysaccharide fractions was present in the humic acid or fulvic acid fractions.     

Studies on soil fumigation—III: Effects on enzyme activities,bacterial numbers and extractable ninhydrin reactive compounds

Fumigation of a field soil with chloropicrin and methyl bromide, either singly or in combination, differentially decreased soil enzyme activities and viable bacterial numbers and increased the amounts of ninhydrin reactive compounds extractable with acidified Tris buffer. Chloropicrin treatment was more effective than methyl bromide.The rates of hydrolysis of both an amide and a peptide derivative were decreased by chloropicrin treatment and remained relatively low despite changes in activities over 325 days. By contrast, caseinase activity initially was decreased by both chloropicrin and methyl bromide fumigation, but activities of the fumigated soils recovered to exceed those of untreated soils. Thereafter, caseinase activities of fumigated and untreated soils exhibited relatively large fluctuations, which were partly associated with seasonal drying of the soils in the field.Chloropicrin but not methyl bromide fumigation markedly depressed the viable bacterial populations, which subsequently increased to be above those of the untreated soils. There was no consistent relationship between the release of ninhydrin reactive compounds following fumigation and changes in bacterial numbers or changes in enzyme activity. Autolytic reactions are probably important in the early stages of amino-nitrogen release in fumigated soils. Net gains in caseinase activity may be partly due to the production de novo of extracellular proteases by microorganisms or to the release of intracellular proteases from killed cells.     

Economic trade-offs to limit nonpoint sources of agricultural pollution

A national model has been built which allows analysis of physical and economic trade-offs as soil loss per acre is limited to specified levels in each major land group of the nation. Crop variables with their associated conservation practices are developed for each of 1891 land groups in 223 agricultural producing regions and 51 water supply regions. The regions and soil groups are made interdependent through regional commodity demands and a transportation submodel. Hence, changes in cropping systems and erosion control practices in one region are simultaneously expressed in effects on other regions. Soil loss limits are set at 10, 5, and 3 t per acre. The 10 t limit does not have a large impact on interregional production patterns and farm comodity prices. However, the 5 and 3 t limits, either singularly or in combination with different export levels, cause rather marked increases in commodity prices. Also at limits of 5 and 3 t, considerable shifts take place among regions in the crops grown and the erosion control methods used. Regions with erosive soils sacrificed in reduced income; regions with level soils can crop more intensely and gain greater income. Conservation practices such as reduced tillage increase the amount of pesticides needed in some regions and pose special environmental problems. The South Atlantic region is affected most by soil loss limits to control nonpoint pollution. The Great Plains regions with more level land and limited rainfall are affected least.     

Determination of amphetamine by Schiff base formation and quantitative gas-liquid chromatography.

A procedure was developed to determine amphetamine salts in solid dosage forms. Amphetamine was extracted from the solid matrix with dilute hydrochloric acid and reacted with cyclohexanone in a strongly basic aqueous methanolic solution. The Schiff base reaction product was extracted with hexane for gas chromatographic determination. Reaction time and optimum conditions were studied. Phenethylamine, similarly treated, was used as an internal standard. Results compared favorably with those obtained by using USP methods.     

Pyrolysis-gas chromatographic analysis of black paints.

Samples of 79 black paints from 27 manufacturers in the United States were examined to determine the extent to which paints can be distinguished by pyrolysis-gas chromatography. Evaluation by a Carbowax column showed some differences among paints from different manufacturers and among batches of paints from the same manufacturer. However, it was not possible to conclude that paints with identical chromatograms had a common origin.     

Some genetic characteristics of the freely drained soils of the ettrick association in East Scotland

This paper describes the interrelated characteristics of the freely drained soil series of the Ettrick Association. These soils are extensively developed in the Southern Uplands of Scotland on glacial drift derived from greywacke.At the present day the soils of the Linhope series are acid brown soils whereas the Minchmoor and Dod series include podzols and peaty podzols. Subalpine podzols and alpine soils are included within the Merrick series. It is concluded that the soils of the Linhope, Minchmoor and Dod series were all formerly brown forest soils under deciduous woodland. They have evolved to their present status after forest clearance which gathered momentum after the widespread establishment of monastic institutions in Scotland in the twelfth and thirteenth centuries A.D. The evolutionary outline of profile development is described and discussed.     

Automated high-pressure liquid chromatographic assay of robenidine hydrochloride.

High-pressure liquid chromatography has been applied to the separation and analysis of robenidine hydrochloride in the presence of its chemical precursors. It provides a rapid and specific method for the analysis of robenidine in technical material as well as feed premixes and is capable of distinguishing the intact drug from its degradation products. The chromatographic system employs a mixture of methanol, acetic acid, and methylene chloride as the mobile phase and a controlled pore glass as the stationary phase. Sample manipulation has been automated in 2 ways. In the first, manually prepared samples are automatically injected onto the column for separation and quantitation. In the second, a totally automated sample handling system, weighed samples are extracted, diluted, filtered, and then injected onto the column, all in a sequential manner. These procedures are capable of giving quantitative results at a rate of 10 samples/hr with a relative standard deviation of 1.13%.