1967
DOI: 10.1080/00275514.1967.12018403
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Rape Seed Extract Agar: A New Medium for Production and Detection of Oospores of Heterothallic Species of Phytophthora

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Cited by 3 publications
(2 citation statements)
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“…The nutrition treatments included reciprocal culturing of all strains with one another and Trichoderma sp. (Brasier et al 1978) on CMA, hemp seed agar (HSA) (Hendrix 1964), soybean agar (SA) (Savage et al 1968), rape seed extract agar (REA) (Satour 1967), carrot juice agar (CJA) (Ershad 1971), mPmTG (Moreau and Moreau 1936a), immersing colonized CMA in glycerine (4%) (Moreau and Moreau 1936b) and culturing the isolates in Petri dishes containing ten boiled hemp seeds in distilled lake water and distilled water (50/50). The temperature treatments also included culturing the isolates in 5, 10, 15, 20, and 25°C in Petri dishes containing ten boiled hemp seeds in distilled lake water and distilled water (50/50).…”
Section: Morphological Identificationmentioning
confidence: 99%
“…The nutrition treatments included reciprocal culturing of all strains with one another and Trichoderma sp. (Brasier et al 1978) on CMA, hemp seed agar (HSA) (Hendrix 1964), soybean agar (SA) (Savage et al 1968), rape seed extract agar (REA) (Satour 1967), carrot juice agar (CJA) (Ershad 1971), mPmTG (Moreau and Moreau 1936a), immersing colonized CMA in glycerine (4%) (Moreau and Moreau 1936b) and culturing the isolates in Petri dishes containing ten boiled hemp seeds in distilled lake water and distilled water (50/50). The temperature treatments also included culturing the isolates in 5, 10, 15, 20, and 25°C in Petri dishes containing ten boiled hemp seeds in distilled lake water and distilled water (50/50).…”
Section: Morphological Identificationmentioning
confidence: 99%
“…The nutrition treatments included (1) reciprocal culturing of all strains with one another and Trichoderma sp. (Brasier et al 1978) on CMA, (2) hemp seed agar (HSA; 60 g/L ground hemp seeds, 15 g/L agar) (Hendrix 1964), (3) soybean agar (SA; 100g/L ground soybean seeds, 15 g/L agar) (Savage et al 1968), (4) rape seed extract agar (REA; 100g/L ground rape seeds, 15 g/L) (Satour 1967), (5) carrot juice agar (CJA; 250 g/L boiled carrot extract, 20 g/L agar) (Ershad 1971), (6) mPmTG (2, 0.4, 0.4 and 12 g/L glucose, tryptone, peptonized milk and agar, respectively) (Moreau and Moreau 1936b), (7) immersing colonized CMA in glycerin (4%) (Moreau and Moreau 1936a) and (8) culturing the isolates in Petri dishes containing 10 boiled hemp seeds in distilled lake water and distilled water (50/50). The temperature treatments also included culturing the isolates in 5, 10, 15, 20, and 25°C in Petri dishes containing ten boiled hemp seeds in distilled lake water and distilled water (50/50).…”
Section: Methodsmentioning
confidence: 99%