Transmission of Pantoea ananatis, Causal Agent of Center Rot of Onion, by Tobacco Thrips, Frankliniella fusca.

Center rot of onion, caused by Pantoea ananatis, was first reported on onion in Georgia in 1997 and has continued to reduce yields and cause postharvest losses. In a previous study, we developed a nondestructive assay that demonstrated an association between P. ananatis and approximately 10% of the tobacco thrips, Frankliniella fusca, surveyed. In this study, we report that all strains of P. ananatis, isolated from surface-sterilized, crushed thrips, were pathogenic when inoculated onto greenhouse-grown onion plants. Furthermore, when 6 to 12 thrips harboring populations of P. ananatis of 1 × 103 CFU ml-1 or greater were placed on healthy onion seedlings to feed, disease transmission occurred in 52% of the plants challenged. Incubation periods ranged from 4 to 9 days. Bacteria isolated from symptoms typical of those associated with center rot were characterized and identified as P. ananatis. In contrast, an equal number of plants remained healthy for up to 28 days after being exposed to the same number of tobacco thrips that were identified as being free of P. ananatis.

Detoxification of dilute acid hydrolysates of lignocellulose with lime.

The hydrolysis of hemicellulose to monomeric sugars by dilute acid hydrolysis is accompanied by the production of inhibitors that retard microbial fermentation. Treatment of hot hydrolysate with Ca(OH)(2) (overliming) is an effective method for detoxification. Using ethanologenic Escherichia coli LY01 as the biocatalyst, our results indicate that the optimal lime addition for detoxification varies and depends on the concentration of mineral acids and organic acids in each hydrolysate. This optimum was shown to be readily predicted on the basis of the titration of hydrolysate with 2 N NaOH at ambient temperature to either pH 7.0 or pH 11.0. The average composition of 15 hydrolysates prior to treatment was as follows (per L): 95.24 +/- 7.29 g sugar, 5.3 +/- 2.99 g acetic acid, 1.305 +/- 0.288 g total furans (furfural and hydroxymethylfurfural), and 2.86 +/- 0.34 g phenolic compounds. Optimal overliming resulted in a 51 +/- 9% reduction of total furans, a 41 +/- 6% reduction in phenolic compounds, and a 8.7 +/- 4.5% decline in sugar. Acetic acid levels were unchanged. Considering the similarity of microorganisms, it is possible that the titration method described here may also prove useful for detoxification and fermentation processes using other microbial biocatalysts.

Effect of fungicide application on activity of Neozygites fresenii (Entomophthorales: Neozygitacaea) and cotton aphid (Homoptera: Aphididae) suppression.

The development of resistance in aphid populations highlights the importance of biological control as a pest management tactic. Four treatments were evaluated to determine the effects of pesticides on the population dynamics of Aphis gossypii Glover and Neozygites fresenii (Nowakowski) Batko: (1) weekly applications of the insecticide imidacloprid (Provado 1.6 F); (2) weekly applications of the fungicide chlorothalonil (Bravo 720); (3) applications of imidacloprid (Provado 1.6 F) when aphid densities exceeded 30 aphids per leaf, and (4) untreated control. Differences in aphid density among the four treatments were shown only to be significant during the 1997 growing season; however, aphid densities were greater in the chlorothalonil treatment than in the other treatments during each growing season. Percentage of N. fresenii-killed aphids was most often highest in the chlorothalonil treatment as well. The fungal epizootic caused by N. fresenii was delayed approximately 1 wk in the chlorothalonil treatment when compared with the other treatments. This delay allowed the aphids to temporarily escape suppression by the fungus and to continue to increase in density until the density-dependent effects of the epizootic overwhelmed the aphid population. N. fresenii also appeared to persist in the system when imidacloprid was in use and does appear responsible for initial aphid reductions. Treatment did not appear to have a large influence on yield outcome. Yield was variable from year to year and from location to location.

Scale-up of an oil/water cream containing 40% diethylene glycol monoethyl ether.

The purpose of this study was to scale up an oil/water (o/w) cream formulation containing 40% diethylene glycol monoethyl ether (DGME), developed via 300-g laboratory batches in a 2(5-2) fractional factorial design, to 7-kg batch sizes in a Brogli-10 homogenizer. The o/w cream was manufactured via a standard phase-inversion process in the Brogli-10 homogenizer. Partitioning studies of DGME were conducted in test tubes at ambient temperature and after 24 hr at 70 degrees C in a convection oven. Phase height was measured by vernier calipers. Microscopy studies of excipients with and without treatment with water or a DGME/water mixture were conducted with a Nikon microscope after equilibration at 35 degrees C for 24 hr. During creation of the 7-kg pilot-scale batches, congealed material was observed between the sweep agitation blade and the discharge port, where the Brogli-10 homogenizer is not temperature jacketed. Factors that increased the amount of congealed material were higher temperatures during primary emulsification and longer cooling times. Partitioning studies revealed that DGME resides in the aqueous external phase of this formulation. Microscopy studies revealed that DGME in the external phase of this cream has a profound impact on the solubility of certain solid, waxy excipients (e.g., cetyl alcohol and polyoxyethylene-2-stearyl ether) at 35 degrees C. From this study, it appears that DGME resides in the external phase of the o/w cream. During manufacturing, it is hypothesized that the presence of DGME in the external phase alters the solubility of certain solid, waxy excipients in the formula such that they no longer primarily reside in the internal oil phase. On cooling, these materials precipitate or congeal in the external phase. The fractional factorial experimental design at the 300-g laboratory scale did not predict the issues encountered during scale-up. Differences between laboratory scale and pilot plant scale that explain why this phenomenon was not seen during laboratory scale are differences in cooling times, nonjacketed or "cold spots" in the Brogli-10 homogenizer, and a low proportion of congealed material in relation to the total batch size (< 1.5%).

Long-term electrical stimulation of rabbit skeletal muscle increases growth of paired arteries and veins.

We tested whether chronic stimulation of skeletal muscle can increase the growth of paired arteries and veins in rabbit extensor digitorum longus muscle (EDL). The right EDL of female New Zealand White rabbits was stimulated via the common peroneal nerve at 10 Hz using 300 microseconds square waves at 3-4 V. Two-hour periods of stimulation was alternated with 4-h periods of rest, 7 days/wk for approximately 60 days. The left EDL served as control. The hindlimb vascular system was maximally dilated and perfuse-fixed with 3% glutaraldehyde and 2% paraformaldehyde at arterial and venous pressures of 80-100 and 15-20 mmHg, respectively. Muscles were postfixed in OsO4 and embedded in EPOX 812 resin. One millimeter-thick transverse sections were cut at uniform locations through the entire breadth of the muscle and analyzed using videomicroscopy along with computerized morphometric and stereological techniques. All paired arteries and veins on each full muscle section were analyzed. Chronic muscle stimulation caused the wall volume of paired arteries and veins to increase by an average of approximately twofold and the lumen volume to increase by an average of approximately threefold compared with the contralateral muscles. The wall-to-lumen area ratio of the arteries and veins was not affected. Muscle stimulation also caused the numerical density of arteries having a diameter > 100 microns to increase by approximately fourfold and the density of veins having a perimeter > 500 microns to increase by approximately 10-fold.(ABSTRACT TRUNCATED AT 250 WORDS)

Miniaturized electrical stimulator with controllable duty cycles.

A stimulator with adjustable duty cycles is described for chronic electrical stimulation of skeletal muscles by way of a motor nerve. The stimulator is unique in that it can stimulate a muscle or group of muscles for 2-h intervals that alternate with variable periods of rest (2, 4, 6, 8, or 10 h). A given duty cycle is selected with a rotary switch at the beginning of an experiment and will continue automatically, without human intervention, for the duration of the experiment. Other features include an adjustable voltage output, a stimulation indicator light-emitting diode (LED), and a low-battery indicator LED. The stimulator is powered by two 9-V batteries or can be used with a bench-top power supply. The stimulation frequency (10 Hz) and pulse width (300 microseconds) are fixed in our design but can be changed to other values by substituting two of the resistors and one capacitor in accordance with simple formulas. We have used the stimulator in rat and rabbit experiments to stimulate the anterior tibialis and extensor digitorum longus muscles for up to 60 days. The timing and output of the stimulator were found to be stable and accurate over the entire 60-day period. The stimulator and batteries were carried in a jacket worn by the rabbits. In the rat experiments, the stimulator was used in a remote fashion with the electrical leads connected to the animals by way of a tethering system. In both animals, the electrodes were implanted adjacent to the common peroneal nerve.(ABSTRACT TRUNCATED AT 250 WORDS)

A stereological method for estimating length density of the arterial vascular system.

We developed a stereological method for quantitating length density (Lv; vessel length per unit reference volume) of the arterial system. Accurate estimation of Lv for a sparse system of blood vessels in a three-dimensional specimen requires information on individual vessel orientation. The method we present extracts the necessary information on vessel orientation from profile geometry. Major and minor diameters of elliptical profiles of sectioned tubular structures are used to calculate Lv. The method does not require special sectioning alignment and does not assume a prior distribution of blood vessels; however, the method does assume that arteries are cylindrical. A physical model consisting of boiled spaghetti mixed with agar in a cylinder was used to test the stereological method. Measurements of over 1,000 elliptical profiles in 5 separate trials have demonstrated that the method can accurately estimate Lv with < 5% error even when tortuosity is high, i.e., when anisotrophy coefficient is 1.55. This method may facilitate a better understanding of the mechanisms of artery growth by making it possible to quantify linear growth of the arterial system.

Effect of surfactants on release of a highly water-soluble medicinal compound from an inert, heterogeneous matrix.

The release from a matrix compressed from a physical mixture of procaine hydrochloride, chlorinated poly(propylene), lactose, and a surfactant was investigated. With nonionic and cationic surfactants incorporated in the matrix, the release of procaine hydrochloride was linearly related to the square root of time, and as the concentration of the surfactants increased, the release was faster. When an anionic surfactant (sodium lauryl sulfate) was incorporated in the matrix, the release of procaine hydrochloride was linearly related to the square root of time; however, the release pattern depended on the concentration of the anionic surfactant. As the concentration of sodium lauryl sulfate increased to 4%, the release progressively slowed to a minimum because of the formation of a poorly soluble complex between the cationic procaine and the anionic surfactant. As the concentration of anionic surfactant increased further, the release increased as the complex was micellarly solubilized.