Field experiments were conducted to determine the population dynamics of Sclerotinia minor and incidence of lettuce drop at two sites during 1995 to 1998. Rotation treatments at the Spence site, which had a low density of inoculum ( 7 sclerotia per 100 cm(3) of soil) that was distributed uniformly, included: continuous lettuce (LLLL), alternate crops of broccoli and lettuce (BLBL), continuous broccoli or lettuce (BBLL), and fallow-lettuce-fallow-lettuce (FLFL). Under continuous lettuce cropping (LLLL) at the Hartnell site, a progressively aggregated spatial pattern of inoculum distribution developed, despite the initial uniform distribution of high inoculum density. In the fallow treatment (FLFL), the spatial pattern tended to be aggregated following a lettuce crop and less aggregated or random when left fallow. In contrast to these two treatments, treatments involving rotations with broccoli (BLBL and BBLL) exhibited consistently random spatial patterns of inoculum regardless of the crop in the field. The marginal increases in the number of sclerotia contributed by the few diseased lettuce plants were offset by the significant reductions in the number of sclerotia by the broccoli residue. Spatial patterns of disease incidence reflected the pattern of inoculum distribution in the soil at the Hartnell site. Higher inoculum density coupled with an aggregated distribution was associated with an aggregation in disease incidence. At Spence, this correlation was poor in most seasons because of progressive decline in the lettuce drop incidence and lack of treatment differences. In greenhouse experiments, the competence volume for S, minor sclerotia was quantified, which was calculated to be 25 cm(3) for 100% infection and 200 cm(3) for 50% infection. Thus, in 100 cm(3) of soil, a minimum of four to five sclerotia are needed for 100% of infection, explaining the high correlation between inoculum density and disease incidence.

Temporal and spatial patterns of lettuce (Lactuca sativa) drop caused by Sclerotinia minor and S. sclerotiorum were determined in lettuce fields in the Salinas, Santa Maria, and San Joaquin Valleys in California during 1995 to 1998. Of the 25 commercial fields assessed, 14 had predominantly S. minor. 9 had predominantly S. sclerotiorum, and 2 had varying levels of both species. Sclerotinia infections were classified based on symptoms: those caused directly by eruptive germination of sclerotia (type 1) and those caused by the airborne ascospores (type 11). The precise location of diseased and healthy plants was mapped and lettuce drop progress was determined at different crop growth stages. Spatial patterns of disease incidence were analyzed using 1-by-1-, 2-by-2-, 3-by-3-. and 4-by-4-m quadrat sizes. Regardless of the analytical method employed, disease incidence with type I infection showed an aggregated pattern in a majority of the fields evaluated and random patterns in fields where incidence was low. In all fields with type I infection, disease progress followed the monomolecular model, typical of soilborne diseases. For fields with aggregated distribution, spatial dependence was observed up to 10 m and was either isotropic or random in direction, suggesting the potential influence of tillage operations on inoculum distribution and disease incidence. Lettuce drop incidence in fields with type II infection was erratic in time and peaked within a very short time. However, disease incidence showed an aggregated pattern in all fields evaluated. Spatial dependence of quadrats generally was detected in two adjacent directions, suggesting a directional gradient perhaps caused by wind direction during ascospore dissemination. Increasing quadrat sizes usually increased the degree of aggregation of lettuce drop, but not the distribution pattern itself. These results demonstrate that the source of inoculum and the type of infections they cause are most likely to determine spatial patterns of lettuce drop in the field.

Sclerotial germination of three isolates each of Sclerotinia minor and S. sclerotiorum was compared under various Soil moisture and temperature combinations in soils from Huron and Salinas, CA. Sclerotia from each isolate in soil disks equilibrated at 0, -0.03, -0.07, -0.1, -0.15, and -0.3 MPa were transferred into petri plates and incubated at 5, 10, 15, 20 25, and 30degreesC. Types and levels of germination in the two species were recorded. Petri plates in which apothecia were observed were transferred into a growth chamber at 15degreesC with a 12-h light-dark regime. All retrievable sclerotia were recovered 3 months later and tested for viability. Soil type did not affect either the type or level of germination of sclerotia. Mycelial germination was the predominant mode in sclerotia of S. minor, and it occurred between -0.03 and -0.3 MPa and 5 and 25degreesC, with an optimum at -0.1 MPa and 15degreesC. No germination occurred at 30degreesC or 0 MPa. Soil temperature. moisture, or soil type did not affect the viability of sclerotia of either species. Carpogenic germination of S. sclerotiorum sclerotia, measured as the number of sclerotia producing stipes and apothecia, was the predominant mode that was affected significantly by soil moisture and temperature. Myceliogenic germination in this species under the experimental conditions was infrequent. The optimum conditions for carpogenic germination were 15degreesC and -0.03 or -0.07 MPa. To study the effect of sclerotial size on carpogenic germination in both S. minor and S. sclerotiorum, sclerotia of three distinct size classes for each species were placed in soil disks equilibrated at -0.03 MPa and incubated at 15degreesC. After 6 weeks, number of stipes and apothecia produced by sclerotia were counted. Solitary S. minor sclerotia did not form apothecia, but aggregates Of attached sclerotia readily formed apothecia. The number of stipes produced by both S. minor and S. sclerotiorum was highly correlated with sclerotial size. These results suggest there is a threshold of sclerotial size below which apothecia are not produced, and explains, in part, why production of apothecia in S. minor seldom occurs in nature.

Field experiments were conducted at Spence Road site and at the Hartnell College East Campus site in Salinas, CA, to determine the effects of crop rotation with broccoli or a fallow period on lettuce drop caused by Sclerotinia minor and the density of pathogen sclerotia in the soil. Treatments at the Spence Road site with low inoculum density (cm(3) Of Soil) distributed randomly included: successive crops of lettuce (LLL), lettuce rotated with broccoli (LBL), and lettuce followed by a fallow period (LFL). Treatments at the Hartnell site with high inoculum density (>7 sclerotia per too cm(3) Of Soil) distributed uniformly included: continuous lettuce (LLLL), broccoli-lettuce-broccoli-lettuce (BLBL), broccoli-broccoli-lettuce-lettuce (BBLL), and fallow-lettuce-fallow-lettuce (FLFL). At the Spence Road site, continuous lettuce did not increase lettuce drop incidence for at least 2 years, although an increase in soilborne sclerotia was observed annually but was below the threshold at which a correlation between inoculum density and disease incidence is observed. Rotation with broccoli resulted in small reductions in disease incidence only in the first year. The density of sclerotia was lowest in the LFL treatment, and the highest in the LLL. At the Hartnell site, rotation with broccoli significantly reduced both sclerotia and lettuce drop incidence. The number of broccoli crops rather than the sequence of lettuce rotations with broccoli was critical for reducing the numbers of S. minor sclerotia in soil. Fallowing after a lettuce crop resulted in marginal reductions in sclerotia and lettuce drop incidence. Viability of recovered sclerotia was not significantly different between treatments, although differences between seasons were detected. Results suggest that rotations with broccoli can be a practical lettuce drop management strategy.

A new method for analysing spatial patterns was designed based on the variance of moving window averages (VMWA), which can be directly calculated in geographical information systems or a spreadsheet program (e.g. MS Excel). Different types of artificial data were generated to test the method. Regardless of data types, the VMWA method correctly determined the mean cluster sizes. This method was also employed to assess spatial patterns in historical plant disease survey data encompassing both airborne and soilborne diseases. The results obtained using the VMWA method were generally different from those obtained with Lloyd's index of patchiness and beta-binomial distribution methods, were in partial agreement with the results from spatial analysis by distance indices, and were highly consistent with the results from semivariogram and spatial autocorrelation analysis methods. Results demonstrated that the VMWA method can be applied to many types of data, including binomial diseased or healthy plant counts, incidence, severity, and number of diseased plants or pathogen propagules although directional and edge effects may limit its application.