Recycling irrigation water is a common practice at ornamental plant nurseries for conserving water; however, it poses the risk of sourcing and dispersing waterborne plant pathogens, especially species of Phytophthora. Slow sand filtration is a water treatment process that can remove pathogens from water, but the slow rate of water treatment may limit its application at nursery operations. In this study, four novel substrates (crushed brick, calcined clay, polyethylene beads, and Kaldnes® medium) in addition to sand were examined to determine how effective each substrate was at removing zoospores of Phytophthora nicotianae from water. The effects of substrate physical parameters, substrate depths (0, 5, 10, 20, 40, and 60 cm), and microbe density (after nursery effluent was recirculated through each substrate for 21 days) on zoospore removal by each substrate were quantified. Sand was the most effective physical filter and supported development of the best biological filter for removing zoospores. Sand columns 40 and 60 cm deep removed zoospores completely using physical filtration alone, and zoospore removal by sand at 10- and 20-cm depths was increased with the addition of biological filtration. Kaldnes® medium and polyethylene beads were the least effective filtration substrates under all conditions tested. After 21 days of recirculating nursery effluent through substrate columns, microbe density in and zoospore removal by all substrates increased. With further optimization, crushed brick may have potential to be utilized as a recycled material for a slow filtration system focused on removing plant pathogens from irrigation water.

Phytophthora nicotianae is currently considered one of the most devastating oomycete plant pathogens, and its control frequently relies solely on the use of systemic fungicides. There is an urgent need to find environment-friendly control techniques. This study examined the chemical composition, inhibitory activity, and possible modes of action of the essential oil of Chrysanthemum indicum L. (EOC) flower heads against P. nicotianae. The EOC was obtained using hydrodistillation at a 0.15% yielded. It inhibited mycelial growth and spore germination of P. nicotianae at a minimum inhibitory concentration (MIC) of 200 μL/L, and exhibited fumigation effects (92.68% inhibition at 157.48 μL/L). Marked deformation of P. nicotianae mycelia included deformed tip enlargement, shrinkage, and rupture. Further, 55 and 47 compounds were identified using gas chromatography-mass spectrometry (GC-MS) and headspace solid-phase microextraction (HS-SPME) GC-MS analyses, representing 88.2% and 98.91% of the total EOC, respectively. Monoterpenes (25.77%) and sesquiterpenes (54.14%) were the major components identified using GC-MS, whereas monoterpenes were the main constituents in the HS-SPME GC-MS analysis. The higher proportions of sesquiterpenes and monoterpenes could be responsible for the inhibitory activity of EOC, which increased mycelia membrane permeability and the content of mycelial malondialdehyde (MDA) in a dose-dependent manner. Cell death also occurred. Thus, destruction of the cell wall and membrane might be two modes of action of EOC. Our results would be useful for the development of a new plant source of fungicide for P. nicotianae-induced disease.