Volatile loss rates of pesticides from turfgrass were measured using the Backward-Time Lagrangian Stochastic Dispersion model (Flesch et al., 1995). Solar radiation, ambient temperature, surface temperature, relative humidity, wind direction, and wind speed were monitored continuously. Growth regulator was applied to the turf plot several days before pesticide application to maintain a constant grass height and aerodynamic roughness length during the experiment. No irrigation occurred following application. Pesticides were applied as mixtures to allow direct comparison of evaporative loss. Mixtures studied were chlorpyrifos + triadimefon + ethofumesate and triclopyr (acetic acid) + propiconazole + cyfluthurin. Airborne flux estimates correlated with temperature, solar radiation, wind speed, time, and vapor pressure of the active ingredient. A log vapor pressure vs. 1/Temperature (K) relationship was observed between flux and surface temperature over a single day for most pesticides. An exponential attenuation of flux was observed over a period of several days and correlated with attenuation of dislodgeable surface residues for two of the pesticides. A fugacity-based model for predicting initial evaporative loss rates from turf grass is presented. Input parameters include pesticide vapor pressure, molecular diffusion coefficient, surface temperature, wind speed profile, atmospheric stability, surface roughness, and average upwind fetch. The GC retention method (Jensen, 1966) was used to estimate pesticide vapor pressures over an environmentally relevant temperature range. The model predicts fluxes that are an order of magnitude greater than measured values. This bias may be due, in part, to deviation from the assumption of pesticide saturated vapor density at the foliar surface. In addition, sensitivity analysis suggests improved estimates of leaf surface temperature and pesticide vapor pressures have the greatest potential to improve model performance. / Graduation date: 2003

The purpose of this research is two fold. First to improve pest management of the sciarid fly (Diptera: Sciaridae) by better defining its relation to mushroom production. Secondly, to explore some of the factors and aspects of the biology of the fly which may increase room to room dispersal rates of adults. The effects of different generations of production room Lycoriella mali Fitch infestations and seasons on yield were explored. In models regressing densities of different generations to mushroom yield, significant negative slopes (p=.05) existed in all models. However, flies did not account for as much yield variance as hypothesized (16.43%). Yield is greatest during the winter months when insect pressure is lowest and decreases in summer months when more insects are present. Diflubenzuron (Dimilin 25 WP, Uniroyal Co.) was tested for its effects on fly emergence and oviposition. Diflubenzuron was effective in suppressing fly emergence and remained effective when treated compost was exposed to phase II peak heating. In production room experiments all fly generations had significantly fewer flies in rooms treated with diflubenzuron at fill. L. mali showed a slight preference to oviposition in diflubenzuron treated compost, indicating a possible attractant effect. A criterion table was developed to estimate the age of L. mali. Both younger and larger L. mali carried more ovarioles. The number of ovarioles that L. mali carry dropped significantly after 48 h; this is likely the time the fly becomes parous. The effects of ambient temperature and distance between production rooms on dispersal were explored. The greatest number of dispersing flies were caught during the summer months. As the daily median temperature increased, the number of dispersing flies increased exponentially. Production room blocks on the perimeter of the farm generally had fewer dispersing flies than centrally located production room blocks indicating that it was unlikely that a reservoir population existed outside the farm. Measurements of wing area and age of L. mali captured while dispersing and not dispersing were compared. Dispersing flies had significantly smaller wings than non-dispersers (p=.000). Wing area for dispersing flies decreased along a density gradient, while wing area for non-dispersers did not. The mean age of dispersing flies was not significantly different (p=.082) from non-dispersers, and neither changed along a density gradient. / Graduation date: 1996

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This item was digitized as part of the Million Books Project led by Carnegie Mellon University and supported by grants from the National Science Foundation (NSF). Cornell University coordinated the participation of land-grant and agricultural libraries in providing historical agricultural information for the digitization project; the University of Arizona Libraries, the College of Agriculture and Life Sciences, and the Office of Arid Lands Studies collaborated in the selection and provision of material for the digitization project.

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Septoria blight of celery (Apium graveolens var. dulce), induced by Septoria apiicola Speg., is a destructive disease that requires fungicide applications for its management. A reliable method of inoculum production was established. Best sporulation was obtained on celery agar (CA) at a predicted optimum temperature of 22.4$ sp circ$C. A moderate inoculum density within a range of 17-35 conidia/cm$ sp2$ of leaf surface provided non-coalescing lesions necessary for rapid enumeration. Initial blight incidence thresholds of about 0.6 and 0.5% to time the first fungicide application were established based on the proportion of maximum plant weight equivalent to the cost of one fungicide application calculated plant weight and petiole number per plant, respectively, in the summers of 1990 and 1991. The IBI levels of 0 and 2% to time the first fungicide application provided non-significant results in terms of the final amount of blight and yield. (Abstract shortened by UMI.)

The use of the larvacidal delta-endotoxin of the sporeforming bacterium Bacillus thuringiensis var. israelensis has been examined as a promising means to control insects that carry diseases such as malaria. An ultimate goal of this project was to genetically engineer both E. coli and the cyanobacterium Synechococcus PCC 7942 to express high levels of this delta-endotoxin and to construct the recombinant to carry a gene which would allow for monitoring of recombinants in the field. Previous research performed by a member of our laboratory involved cloning the gene fragment encoding the delta-endotoxin into a hybrid plasmid yielding recombinant E. coli clones which were toxic to mosquito larvae. Unfortunately, upon further examination of these recombinants using agarose gel electrophoresis and mosquitocidal assays, the clones were found to be unstable and lost their toxin encoding genes readily. Furthermore, cloning of the stabilizing parB locus into one of the recombinant plasmids did not enhance segregational stability as had been shown with some plasmids in E. coli. In another approach oligonucleotide primers were constructed which flanked the 130 kDa toxin gene but excluded a transposon-likesequence postulated to contribute to instability. These primers were used in the polymerase chain reaction in order to amplify this smaller DNA fragment for cloning experiments. Only a small quantity of primers were made and amplification of the DNA was not achieved prior to depletion of the primers. Future work will involve synthesizing new primers to be used for amplification and cloning of the B.t.i. toxin gene.In order to construct a traceable recombinant, the luciferase reporter gene (Luc) had been previously cloned into a hybrid plasmid that was capable of transforming both E. coli and the cyanobacterium Synechococcus PCC 7942. The new construction was then transformed into E. coli, to yield a pool of uncharacterized recombinants. In the present work, I determined that the luciferase enzyme was being expressed in the E. coli recombinants in the presence of the substrate luciferin. Initially, bioluminescence of these E. coli clones was detected by using OG-1 film which fogs in the presence of light. In order to quantify expression of the clones, lysates of the E. coli recombinants were also examined using a luminometer. Comparisons of bioluminescence were made between lysates with the parent E. coli plasmid harboring the luciferase gene and recombinants in which the Luc gene was placed downstream of the powerful rightward lambda promoter. Luminometer readings indicated that luciferase expression was enhanced six fold (from 2.0 X 10-6 to 3.0 X 10-5 by units/cell) in the recombinant plasmid. Plasmid DNA was isolated from the two luciferase expressing E. coli clones. Recombinants were obtained as determined by agarose gel electrophoresis examination of the plasmid DNA. This recombinant DNA was used to transform Synechococcus PCC 7942. However, because enzyme releasing methods were unsuccessful for the more rigid Synechococcus PCC 7942, the level of expression of the Luc gene could not be determined by either method mentioned above. Apparently, the methods used either failed to lyse the cells or they were too harsh and inactivated the enzyme. Future endeavors will involve the use of a French press to more gently lyse the cells so that the level of expression can be determined. / Department of Biology

Septoria blight of celery (Apium graveolens) caused by Septoria apiicola is a common disease. This work dealt with the development of a simple forecast model to time fungicide application to manage the blight. Two studies were conducted to examine the effect of relative humidity (65, 88, 92, 96%, and wet) temperature (15, 20, 25, and 28 C) and exposure period (6, 12, 24, 48, 72, and 96 hr) on spore production. Spores were produced at all levels of relative humidity and temperature tested. Overall spore production increased with increasing relative humidity. The greatest and the least were produced after a 48 hr wet period at 20 and 28 C, respectively. Two regression models were developed to predict spore production as functions of relative humidity and temperature. In order to validate the infection function model a field experiment was conducted in 1989 to quantify latent period. A mean latent period beginning of 12 days, a mean latent period 50% of 14 days, and a mean latent period ending of 19 days were established. Two regression models were developed to predict latent period beginning and latent period ending as functions of mean maximum and mean minimum temperatures. In order to develop a simple forecast model field experiments were conducted in 1989 and 1990. From these studies two simple forecast models are proposed to initiate fungicide applications: (1) Initial disease occurrence. (2) A cumulative disease severity value (CDSV) of 23. Using the forecasts proposed it is possible to reduce five to seven applications of fungicides during the celery growing season in Quebec.

Forecasts for the first fungicide application to manage cercospora blight of carrot (Daucus carota L. subsp. sativus (Hoffim) Arcang) caused by Cercospora carotae (Passerini) Solheim were evaluated during the summers of 1991 and 1992. In the forecast based on infection, the blight severity values (BSV) were calculated for each day using duration of leaf wetness, relative humidity and temperature. The first fungicide was applied when the cumulative blight severity value reached 14 (CBSV 14) and 18 (CBSV 18). The forecasts were compared with the 50% disease incidence threshold method where the first fungicide was applied when the middle leaf of 50% of plants was diseased, and the conventional method where the first fungicide application was made when the plant height reached 15 cm. For the threshold of CBSV 14 and CBSV 18, no loss was observed in yield and fewer fungicides were applied as compared to conventional and 50% disease incidence threshold methods. Three years of weather data from experimental plots and 155 commercial field data were used to study the behaviour of CBSV at 50% disease incidence threshold. Only in 3% of the fields, the disease incidence of 50% was observed before the CBSV reached 11. The increase from CBSV 11 to 20 was rapid. Depending on environmental conditions the first fungicide at a CBSV range of 11 to 20 is proposed rather than a critical threshold since no loss in yield was observed at 18 in the experimental plots. No fungicide is applied until the CBSV reaches 11 and the application must not be delayed after CBSV reaches 20.

Bibliography: leaves 132-185. / 113 leaves : ill. (some col.) ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Thesis (Ph.D.)--University of Adelaide, Dept. of Soil and Water, 2000