Apparatus and procedure for measuring release rates from formulations of lepidopteran semiochemicals

An apparatus was developed wherein a vacuum source was used to pull air across a controlled-release-formulation dispenser or a planchet containing a known quantity of a semiochemical and into a collector filled with a polymeric adsorbent. After a set time, the semiochemical was eluted with solvent and was quantified by gas-liquid chromatography (GLC). High percentages of known quantities of the lepidopteran semiochemicals (Z)-7-dodecen-l -ol acetate (Z7DDA), boiling point (bp) 275 ° C/1 atm, (Z)-9-tetradecen-1-ol formate (Z9TDF), bp 289 °C/1 atm, and (Z,Z)-3,13-octadecadien-1-ol acetate (ZZODDA), bp 490 °C/1 atm, were recovered. The semiochemicals did not oxidize and were recovered quantitatively from the adsorbent. The release rates of Z9TDF from a controlled-release dispenser were found to be directly proportional to the airflow rates. Release rate measurements on the Z9TDF dispensers were made for the purpose of estimating the method's precision. The method was shown to give internally consistent results by measurements on another Z9TDF formulation. The accuracy of the method is discussed.Mention of a commercial or proprietary product in this paper does not constitute an endorsement by the USDA.     

Necrodols: Anti-insectan terpenes from defensive secretion of carrion beetle (Necrodes surinamensis)

Two compounds recently isolated from the defensive gland ofNecrodes surinamensis, -and -necrodol, first representatives of a new category of monoterpenes (the necrodanes), are shown to be repellent to ants and other insects and irritating to cockroaches and flies. The compounds doubtless play a defensive role inNecrodes. The possible long-range applied significance of research on insect repellents is discussed.Paper No. 80 of the seriesDefense Mechanisms of Arthropods. Paper No. 79 is T. Eisner et al., Experientia 42:204–207 (1986).     

Strain-Induced Deformation in Magnesia–Alumina Layered Composites

Ceramic beams are induced in situ to form complex shapes at elevated temperature without the application of an external stress. This process has been demonstrated for thin alumina substrates coated with a layer of magnesia. The internal strain causing the substrates to deform at elevated temperature arises as a consequence of strain mismatch accompanying the penetration of the coating into the substrate. The magnitude of the deformation depends on the amount of coating applied, on the thickness of the substrate, on the density of the substrate, and on the temperature. During exposure of the beams to elevated temperature, the magnesia coating reacts with the alumina substrate to form the spinel phase; the resulting volume change accompanying the phase transformation is likely the predominant driving force for deformation.     

Determination of water in cooked cottonseed meats by a modified indirect conductivity method

Summary The modified indirect conductivities and oven-dry moisture percentages were determined on mine Samples of cooked cottonseed meats (1.8 to 13.9% water). Statistical treatment of the data yields the following results: (1) equation of the regression line, {fx177-1} (2) correlation coefficient, 0.998; (3) standard deviation from the regression line, 0.27% water. Ten replicate determinations made on each of two samples containing 2.7 and 7.7% water showed standard deviations of 0.07 and 0.08% water. These results show that the accuracy and precision of the modified indirect conductivity method are satisfactory for practical applications. For a consecutive series of determinations the average time required per determination was about 9 min. This time could be reduced to about 5 min. by using duplicate sets of stirring apparatus. Describes data obtained in research conducted cooperatively by the Cotton Research Committee of Texas and the Texas Engineering Experiment Station.     

Thermal degradation studies of several pyrrone films

The thermal degradation of several polyimidazopyrrolone (pyrrone) films was studied in air and in vacuum over the range of 100–1000°C. by thermogravimetric analysis (TGA), with the use of both isothermal heating and programmed heating rates of 2, 3, 5, and 7.5°C./min. At pressures of 10^?6 torr or less, maximum weight losses average 30% at 800°C. Rates of volatilization and activation energies were derived to provide comparison between these ladder-type polymers. Mass spectrometric analysis of the pyrolysis gases evolved under vacuum conditions showed that CO, CO₂, and H₂O were the primary volatile products and that they were formed throughout the period of weight loss. Approximate correlation between changes in weight and changes in the total pressure for the vacuum tests indicates that mass spectrometric results could provide quantitative as well as qualitative data. The importance of sample history prior to heating and of sample geometry in developing meaningful and reproducible TGA results is aptly demonstrated. The ability of these materials to absorb readily 5–7 wt.-% of water under ambient conditions and the effect of this property upon weight loss measurements are shown.     

Characteristics of the lipase from the mold,Geotrichum candidum: A review

The moldGeotrichum candidum produces an extracellular lipase, readily concentrated by removal of the culture medium in which the microorganism is grown. The lipase is characterized by a unique, but not absolute, specificity for fatty acids containingcis-9 orcis,cis-9, 12 unsaturation, hydrolyzing both regardless of position within the triglyceride molecule. The enzyme also hydrolyzescis-9-16∶1,cis,trans-9,12-18∶2,trans,cis-9,12-18∶2, palmitoyl oleate and cholesteryl oleate. Digested at comparatively slow rates are:trans,trans-9,12-18∶2, double bond positional isomers of 18∶1 (other thancis-9), stearolic acid, oleoylpalmitate, dilinoleoyl phosphatidyl choline, and saturated acids. The enzyme has an optimum pH of 8.2, and the lyophilized powder is extremely stable, retaining activity for at least eight years when stored at-20 C. A purification of 81-fold has been achieved. One of five papers presented in the Symposium “Microbial Lipolytic Enzymes,” AOCS Spring Meeting, New Orleans, April 1973. Scientific contribution 556, Agricultural Experiment Station, University of Connecticut, Storrs, Conn. 06268.     

Polymerization mechanisms and molecular weight distribution. II. AIBN-initiated polymerization of styrene at 60°C

An experimental study was carried out on the AIBN-initiated polymerization of styrene at 60°C. The kinetic rate constants were determined by the method of moments and the MWD method, which was proposed in a previous paper. The results compared favorably with the data in the literature and the MWD method was noted to yield more consistent results than the method of moments, which indicates the importance of considering the whole molecular weight distribution. The theoretical MWD was found to approximate the experimental MWD well. The chain-transfer constant to AIBN was found to be between 0.09 and 0.14.     

Isolation and characterization of ganglioside 9-O-acetyl-GD3 from bovine buttermilk

Bovine buttermilk contains a unique ganglioside, 9-O-acetyl-GD₃. In order to isolate large quantities of this ganglioside, a simplified isolation scheme which consists of several ion-exchange and silica gel column chromatographic procedures was devised. The isolated 9-O-acetyl-GD₃ was characterized on the basis of its thin-layer chromatographic behavior, its immunoreactivity with a specific monoclonal antibody, JONES, and by conversion to authentic GD₃ by mild base treatment.     

A model for studying LCAT reaction: In vitro cholesterol esterification in pig ovarian follicular fluid

Phosphatidylcholine acyltransferase (lecithin:cholesterol acyltransferase or LCAT; EC 2.3.1.43) activity was found to be present in pig ovarian follicular fluid (POFF), in addition to pig serum (PS). The cholesterol esterification rate in both POFF and PS is linear with incubation time up to 2 hr. The mean absolute rate of POFF-cholesterol esterification was 8.1±0.4 nmoles per ml per hr approximately one-fourth of that in PS. However, the fractional rate (percent of labeled cholesterol esterified per hr) of POFF-cholesterol esterification was similar to that observed in PS. There was little variation of absolute rate of cholesterol esterification in the fluid obtained from different sizes of follicles. Fatty acid or triacylglycerol did not participate in the reaction of cholesterol esterification in POFF. No appreciable change in enzymatic activity was found from storing POFF at 4 C for periods of time up to 24 hr or at −70 C up to 2 months, but activity was lost thereafter. On the other hand, PS showed a much longer period of stability (5 days at 4 C and 9 months at −70 C). A discrepancy between the fatty acid composition of cholesteryl esters formed by the LCAT reaction and the fatty acid composition at the C-2 position of phosphatidylcholine led us to propose a two-step mechanism for the LCAT reaction. It is concluded that the LCAT of POFF, as well as that of plasma, is specific for individual fatty acids rather than for the fatty acid composition of phosphatidylcholine. The fatty acid concentration of lysophosphatidylcholine decreased during prolonged incubation times (6 to 21 hr) suggesting that the increased lysophosphatidylcholine formed as a product of the LCAT reaction may be reused as substrate for the LCAT reaction or for hydrolysis by lysophosphatidylcholine hydrolase. Presented at the AOCS Meeting, New York, May 1977.     

Radical entry mechanisms in redox-initiated emulsion polymerizations

The mechanisms and kinetics of radical entry in emulsion polymerizations utilizing redox initiation are investigated using polymerization rate data obtained by reaction calorimetry and electrospray mass spectroscopy analysis of initiator-derived aqueous-phase products. These data have been used to evaluate an initiation scheme for redox-initiated emulsion polymerizations of common monomers such as styrene and methyl methacrylate based around the oxidant, tert-butyl hydroperoxide. Redox initiators are broadly classed by the solubility of their radical products: Hydrophilic radicals enter by propagating to a critical degree of polymerization to become surface-active whilst more hydrophobic radicals may enter particles directly. When direct entry is applicable (the hydrophobic case), initiation efficiency will always be very high.