<mods:mods version="3.3" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-3.xsd" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><mods:titleInfo><mods:title>A Technique for Phytophthora drechsleri f. sp. cajani Sporangia and Zoospores Production</mods:title></mods:titleInfo><mods:name type="personal"><mods:namePart type="given">J</mods:namePart><mods:namePart type="family">Kannaiyan</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">V K</mods:namePart><mods:namePart type="family">Sheila</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">Y L</mods:namePart><mods:namePart type="family">Nene</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:abstract>Cultures on V-8 juice agar medium were incubated for 5 d at 30°C, then 5 mm diam. discs were removed from the periphery of the colonies and floated in clear V-8 juice and sterile distilled water (1:5) for a further 24 h at 30° under fluorescent light. The mycelial discs were rinsed twice in sterile distilled water and incubated again under the same conditions in sterile distilled water. Abundant sporangia were produced in 16 h and suspensions of c. 50 000 zoospores/ml were obtained.</mods:abstract><mods:classification authority="lcc">Pigeonpea</mods:classification><mods:classification authority="lcc">Fertilizer Applications</mods:classification><mods:originInfo><mods:dateIssued encoding="iso8061">1994</mods:dateIssued></mods:originInfo><mods:originInfo><mods:publisher>International Crops Research Institute for the Semi-Arid Tropics</mods:publisher></mods:originInfo><mods:genre>Article</mods:genre></mods:mods>