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Relationships between disease incidence at two levels in a spatial hierarchy
Phytopathology
|May 1, 1997
Summary
Disease incidence relationships across spatial scales were analyzed using binomial and beta-binomial distributions. Higher-scale incidence is an asymptotic function of lower-scale incidence and aggregation, impacting disease spread modeling.
Area of Science:
- Plant pathology
- Spatial statistics
- Epidemiology
Background:
- Understanding disease incidence across hierarchical spatial scales is crucial for effective disease management and sampling strategies.
- Existing models often simplify spatial relationships, potentially overlooking the impact of aggregation on disease spread.
- The binomial and beta-binomial distributions provide frameworks for analyzing count data, but their application to hierarchical spatial disease incidence requires further investigation.
Purpose of the Study:
- To derive and test relationships between disease incidence measured at two levels of a spatial hierarchy.
- To investigate the influence of aggregation and sampling unit size on disease incidence across scales.
- To develop methods for estimating disease variance at a lower spatial scale from higher-scale measurements.
Main Methods:
- Utilized properties of the binomial distribution and beta-binomial distribution.
- Applied an empirical power-law relationship linking observed and theoretical binomial variance of disease incidence.
- Tested relationships using observational data for grape downy mildew, citrus tristeza, and citrus scab.
Main Results:
- Disease incidence at a higher spatial scale demonstrated an asymptotic relationship with incidence at the lower scale, degree of aggregation, and sampling unit size.
- For random disease patterns, the cross-scale incidence relationship was parameter-independent.
- Derived an equation to estimate lower-scale disease variance from higher-scale incidence measurements for sampling purposes.
Conclusions:
- Aggregation of disease at a lower spatial scale reduces the rate of incidence increase at a higher spatial scale.
- The derived relationships offer a more nuanced understanding of spatial disease dynamics.
- The findings support improved disease sampling and modeling by accounting for spatial hierarchy and aggregation.
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