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ThesisItem Open Access Deterioration of oil cake by fungi(Department of Plant Pathology, College of Agriculture, Vellayani, 1989) Naseema, A; KAU; Wilson, K IFungi causing deterioration of coconut, groundnut and sesamum oil cakes were studied. ficremonium implicatum, Asperdllus aculeatus, A. flavus, A. fumigatus, A. nlaer, A. terreus, A. versicolor, Bipolaris hawaiiensis, Curvularia clavata, Monascus ruber, Penicillium aurantioqriseum, P. Pinophilum, Pestalotiopsis palmarum, Rhizomucor £usillus and Ehizopus stolonifer were obtained from coconut oil cake. Aspergillus flavus, A. niaer, A. terreus, A. versicolor, Gliocladium sp. Penicillium pinophilum, RhizoEUS or^zae and Rhizopus stolonifer were noticed in groundnut and Aspergillus candidus, A. flavus, A. fumigatus, A. nlaer, A. tamarii, A. terreus, Curvularia clavata, Eurotium. chevalieri, F"sarium pallidoroseum, Monascus ruber, Fenicilliuiu pinophilum, Pestalotiopsls palmarum and Rhizopus or^zae in sesamum oil cake. Of these, Acremonium implicatum, Aspergillus aculeatus, A. caeslellus, A. .f"-igatus, Bipolaris hawaiiensis, Curvularia clavata, Monascus ru^, Penicillium anrantlogriseum, P. pinophilum, Pestalotiopsls palmarum and Rhizomucor pusillus from coconut oil cake, Aspergillus versicolor, Gliocladium sp., Penicillium pinophilum, Rhizopus oryzae and R. stolonifer from groundnut and Aspergillus candidus, A. fumigatus, A. tamarli, A. terreus, Curvularia clavata, Eurotium chevalieri, Fusarium pallidoroseum,Monascus ruber, Penicillium pinophilum, Pestalotiopsis palmarum and Rhizopus oryzae from sesamum oil cake have not been reported earlier. * Aspergillus flavus and A. niger were isolated from all the samples of groundnut and sesamum oil cakes. In coconut oil cake, these two fungi were present in 88.89 and 77.78 per cent of the samples. A. terreus was isolated from 66.67 per cent of groundnut and 55. 56 per cent of coconut and sesamum oil cake samples. Penicillium pinophilum was obtained from 66.67 per cent of groundnut, 44.44 per cent of sesamum and 27.78 per cent of coconut oil cake samples. Wide variation was noticed in the population of fungi present in the oil cakes collected from different regions during different periods of the year. Oil cakes collected during June-July had the highest population, of fungi. The central and the northern regions recorded higher population of fungi than the southern region. Positive and significant correlation could be obtained between weather parameters and population of fungi in different oil cakes. Maximum correlation was noticed in relation to total rainfall. Qood mycelial growth of fungi was obtained in all the oil cakes incubated at 27, 29 and 32°C. Maximum mycelial growth was noticed at 100 per cent relative humidity. This was followed by 96.1 per cent and 92.9 per cent in the descending order. The oil content of the oil cakes was considerably reduced due to the growth of all the fungi tested individually and in combination. Maximum reduction v/as noticed due to the growth of Pestalotiopsis palmarum in coconut oil cake, Rhizopus stolonifer in groundnut and Fusarium pallidorosem in sesamum oil cake. In the case of combinations, Aspergillus flavus, A. niger and Penicillium pinophilum together caused maximum reduction in oil content of coconut oil cake. In groundnut, combined growth of A. flavus, A. niger and A. terreus caused maximum reduction in oil whereas, A. niger and P. pinophilum together effected maximum reduction of oil in sesamum oil cake. Oil cakes inoculated with different fungi showed considerable reduction in total carbohydrates, crude protein, free amino nitrogen, crude fibre and ash to the extent of 6.11 to 76.95 , 4 . 28 to 68.03, 14.91 to 92.52, 1.25 to 92.55 and 0.17 to 65.16 per cent respectively. In the case of mineral nutrients like phosphorus, potassium, magnesium. calcium, copper and iron reduction ranging from 15.07 to 75.54, 23.13 to 94.41, 10.89 to 63.37, 28.78 to 90.20, 52.52 to 97.12 and 0.32 to 60.77 per cent respectively was noticed. Fourteen out of 2 0 isolates of Aspergillus flavus produced aflatoxins B^, and G2 in culture medium with maximum quantities being 1210, 1040 and 151 ppb respectively by the isolates from coconut oil cake. Eight out of 19 isolates of A. niger elaborated upto 222 ppb by the isolate from sesamum oil cake. When grown on the respective host material, A. flavus isolates from coconut oil cake produced maximum quantity of B^^, B^ and being 1517, 1092 and 272 ppb respectively. A. niger isolate from coconut oil cake produced B^^ upto 419 ppb. oil cakes treated with calcium propionate (0.6 per cent, w/w) were free from fungus growth throughout the period (180 days) of observation and showed minimum number of fungal propagules whereas, those kept as control had higher population of fungi than the treated ones, at all period.of observation. Oil cakes stored in polythene lined gunny bags had the least population of fungi, whereas those stored in ordinary gunny bag had very high population of fungi. These results revealed that fungal deterioration and spoilage of oil cakes could be prevented or reduced to the minimum by treatment with 0.6 per cent calcium propionate- and by using polythene lined gunny bags for storage arid transport.ThesisItem Open Access Study of bacterial leaf spot of betel vine- biochemical changes and control(Department of Plant Pathology, College of Agriculture, Vellayani, 1986) Koshi, Abraham; KAU; James, MathewThe bacterial leaf spot is one of the most serious diseases of betel vine in Kerala. The bacterium is one of the most serious disease of betal vine. Confidering the seriouness of the disease , studies were undertaken on the different aspects of the disease and to find out a suitable control /management practice.ThesisItem Open Access Varietal screening of banana against anthracnose disease(Department of Plant Pathology, College of Horticulture, Vellanikkara, 1984) Srinagesh, K L; KAU; Jose, P CLaboratory and field studies of the varietal screening of banana against anthracnose disease were conducted at the college of Horticulture. Vellanikkara and at Banana Research Station, Kannara respectively during 1981-1983. In the field the infection started at the distal end of the banana fruit and in course of time the infected fruit became blackened, shriveled and mummified. After Harvest, the symptoms appeared as small brown spots which enlarged quickly and coalesced forming larger patches. The affected areas were covered with orange to salmon pink coloured conidial masses. The detailed morphological studies of the fungus proved that the anthraemose disease of banana is caused by colletrichum cloeosporioides cooko and massee, the imperfect stage of glomerella cinoulata spauld and shrenk. Twenty five varieties of banana fruit were screened in vitro at different stages of development against anthracnose disease. The varieties showed different degrees of susceptibility at various developmental stages of the fruit. The pooled analysis of the data showed that the variety nendra padaththi followed by palayankodan, jurmani kunthali, boodida bontha bathes, peyan, kanchikela, pisang mas and kapok were found to be highly resistant. The varieties Zanzibar, adakka kunnan, klue teparod, chinia, nendran, venneettu mannan, koduppilla kunnan, hybrid sawai, poocha kunnan, red banana and boodles altafort were found to be resistant to the disease. The variety robusta was found to be susceptible. The varieties njalipoovan, pisang lilin, dwarf Cavendish, matti and gros Michel were found to be highly susceptible. The major chemical constituents of banana fruit viz. reducing sugars, total sugars starch, crude fibre, crude protein and tannin at different developmental stages of twenty five varieties were analysed. The reducing sugars and total sugar were found to increase steadily from immediately after female phase to ripened stage in all the varieties. The starch and crude fibre contents, though increased steadily upto full maturity. Declined sharply at the ripening stage. The crude protein and tannin contents were maximum at immediately after female phase but steadily decreased and were minimum at ripening phase. There was a significant positive correlation between reducing sugars, total sugars and per cent disease intensity at three fourth maturity. High sugars were responsible for susceptibility to the disease. A significant negative correlation was obtained between crude protein and per cent disease intensity at half maturity. A significant negative correlation was also obtained between tannin and per cent disease intensity at one fourth and half maturity stages. High crude protein and high tannin contents were responsible for resistance to the disease.ThesisItem Open Access Symbiosis of rhizobium and VA mycorrhiza in subabul(Department of Plant Pathology, College of Agriculture, Vellayani, 1989) Rajendran Pillai, M V; KAU; Sasi Kumar NairA survey was conducted at 17 locations in four districts of Kerala for natural nodulation and VA mycorrhizal infection in subabul. The survey revealed that natural nodulation and VA mycorrhizal infection were poor compared to inoculated plants. When all the 17 isolates of rhizobia and four cultures of VA mycorrhizal fungus were tested for effectiveness, the rhizobial isolate R8 and V AM fungus M2 were emerged as most efficient rhizobial and mycorrhizal cultures respectively. An in vitro study conducted revealed that in an acid PH of 6, the rhizobial isolate R8 survived better than other cultures. At pH 8, growth of another isolate R5 was found maximum. However, in an in vivo study, there was not much significance for the soil pH ranging from 6 to 7.1 in influencing various biometric parameters of subabul. In both the pH of 6 and 7.1, the performance of rhizobial isolate R5 and mycorrhizal culture M2 was best. Serological studies revealed that the exotic strains R18 R20 and and isolate from Mimosa indica had serological similarities with the best selected local isolate R8. Fine structure studies of nodules clearly showed the morphological differences between the uninfected nodular tissues and the infected central nodular tissue. The rhizobial infection transformed the normal cells into irregularly shaped cells within which numerous rhizobial cells were visible. In another observation, it was found that subabul plants starts to form nodules only from 15 days of sowing. There- after, the nodule number increased steadily attaining the peak at 70 days of growth and then remained more or less steady. Among various methods of inoculation of the microsymbionts tested, inoculation of both the microsymbionts at the time of sowing in polybag was found good for the better establishment of the plants in the field. In a field study, it was found that inoculation of the local isolate of Rhizobium R8 and mycorrhizal fungus M2 had great influence in increasing all the growth parameters. Standard mycorrhizal culture and local isolate performed equally well. Maximum forage yield was obtained when plants were inoculated with the selected local rhizobial isolate R8 and mycorrhizal fungus M2. Maximum mycorrhizal infection was also seen in the same treatment. Dual inoculation also had significant influence in increasing the leaf protein content. An important observation was that both rhizobial and mycorrhizal inoculation reduced the mimosine content of leaves. However, fertilizer nitrogen increased mimosine content. In short, dual inoculation by Rhizobium and VA mycorrhiza was found necessary for better establishment, growth and low mimosine content of subabul.ThesisItem Open Access Ochratoxicosis in the goat(Department of Pathology, College of Veterinary and Animal Sciences, Mannuthy, 1983) Maryamma, K I; KAU; Krishnan Nair, MAn experimental study was carried out to delineate the pathological effects of ochratoxin in goats. A comparative assessment of ochratoxin production by A. ochraceus and A. sulphureus on what and rice under static and shake cultures was also made. A. ochraceus was found to be a better toxin producing strain in both substrates under static and shake cultures systems and wheat was a better substrate than rice. Toxicity studies were conducted in Sannen – Malabari cross-bred goats of 1 to 3 months age. Purified ochratoxin produced in the laboratory was administered by oral, intra-peritoneal and intravenous routes. The different dose levels adopted were 2.5 mg/kg body weight, 1 mg/kg body weight and 0.5 mg/kg body weight. The synergistic effect of ochratoxin and aflatoxin in goats was studied by adminstering the crystalline toxins simultaneously (Makor Chemicals, Israel) by itraperitoneal route. The parameters of study were: clinical signs, haematological and biochemical alterations, pathological changes in urine, and macroscopic, microscopic and ultra-structural alterations in organs. Varying degree of clinocopathological changes were noticed in the test animals. The animals became weak and listless and in general there was reduction of total erythrocyte count, PCV, haemoglobin and lymphocyte count. Serum protein level was lowered while BUN and creatinine and blood coagulation time were high. There was rise in ALP, SGOT and SGPT in some of the test animals. The changes and degree of variation depended on the dose, total quantity and rate of administration of the toxin and duration of the experiment. More severe alterations were noticed when ochratoxin and aflatoxin were administered simultaneously. Important changes in the urine were lowering of pH, albuminurea and presence of epithelial cells and casts. Pathological changes varied in severity in different organs and were observed in the following descending order: kidney, liver, intestines, stomach, lymph nodes, spleen, thymus, genital organs, endocrines. In the kidneys, the order of intensity of pathological alterations was: proximal convoluted tubules, Henle’s loop, distal convoluted tubule, glomeruli, collecting tubules. Retrogressive changes of different degree and necrosis of the lining epithelial cells of tubules and endothelium and epithelium of glomeruli were the important lesions. Changes in glomeruli and Bowman’s capsule noticed in the higher dose group included shrinkage of glomeruli and presence of proteinaceous material in the capsular space. Eosinophilic granular casts and PAS positive bodies were present in the lumen of tubules. The necrobiotic renal changes were more intense when orchatoxin and aflatoxin were administered simultaneously. Hepatic lesions were mainly fatty infiltration, necrosis of hepatocytes and haemorrhage. The changes were most severe in combined toxicity. Mallory bodies and mild biliary hyperplasia were noticed in a few sections. Necrosis and subsequent depletion of lymphocytes wee the lesions in lymph nodes, spleen and thymus in some test animals. Degenerative changes were also noticed in testis, ovary, pituitary, adrenals and pancreas in experimental groups. In the combined toxicity group the pathological effect was more intense. At the ultra-structural level, the hepatcytes as well as the epithelial cells in the kidney showed severe changes. The cell organelles were either completely damaged or showed partial configurational alterations. Mitochondria showed changed in the density of matrix as well as disorientation and destruction of the limiting membranes and cristae. Cytolysosomes incorporating damaged cell organelles were abundant. Disaggregation of ribosomes and fragmentation of ER were noticed. In the glomerulus, there was destruction of the basement membrane and disruption of the regular arrangement of the foot processes of podocytes. In the cytoplasm of hepatocytes, Mallory bodies and lipid droplets were present. Varying degree of nuclear changes like clumping, condensation and disappearance of chromatin and fragmentation of nucleolus and nuclear membrane were observed. Changes occurred in the tight junctions of epithelial cells of bile ducts. Pathological alterations were more pronounced when ochratoxin was administered by the pwerenteral route. Oral administration of toxin also effected structural alterations which indicated that some fraction of ochratoxin escaped degradation in the rumen. From this study it became evident that aflatoxin potentiated the effect of ochratoxin. The structural damage to the cells might be due to the inhibition of oxidative enzymes which is reflected by the extensive ultra- structural alteration observed in the mitochondria and RER. Biochemical changes like high BUN and creatinine were evidently due to necrobiotic changes in the kidney. Interference in the synthesis of proteins due to damage of hepatic cells and escape of protein molecules due to alteration in the podocyte foot processes and basement membranes may account for the reduced serum protein levels. The nature of organellar destruction and configurational changes in the cells indicate the toxic potency of the mycotoxin on the biological system.ThesisItem Open Access Studies on purple top roll (PTR) of potato in Karnataka(Department of Plant Pathology, University of Agricultural Sciences, Bangalore, 1983) Sreedharan, A; KAU; Reddy, H R1. Survey for the incidence of potato purple top roll revealed that the disease was present in Bangalore, Belgaum, Dharwad, Hassan and Kolar districts of Karnataka. The average percentage of incidence varied from 8.94 to 50.07. The survey also indicated that there was low incidence of the disease in summer and high incidence in kharif and rabi. 2. The pathogen was transmissible by wedge, side and core grafting. 3. The disease was transmitted through dodder, Cuscuta chinensis Lam. 4. The disease was not transmissible through sap and aphids Myzus persicae Sulz. And Aphis gossypil Glov. 5. The etiological agent was transmitted by the leafhopper, Orosius albicinctus Distant and not by Hishimonus phycitis Distant. 6. The vector, O. albicinctus could acquire the pathogen in two hr and inoculate to healthy plants in 30 min. The percentage of active transmission was 35 – 40 and the minimum incubation period in the plant was between 20 and 25 days. Maximum percentage of transmission was obtained on 40th day after inoculation. 7. Characteristic symptoms of the disease was inward rolling of basal parts of top leaflets, purple/pink pigmentation, smalling of leaves, excessive proliferation of axillary buds, erect appearance, production of purple coloured, aerial tubers and stunting and dwarfing of plants. 8. The etiological agent infected tomato, tree tomato, Datura stramonium and D. metel by grafting. 9. The pattern of spread of the disease in the field was from external source in the beginning and later the spread was within. 10. The vector population was correlated with the disease incidence in the field. The increase in the incidence of the disease followed the increase in the vector population. 11. The leafhopper vector, O. albicinctus Distant was high in the months from late June to December and low from January to early June. 12. The high population of leafhoppers was correlated with low temperature and high humidity and low population was correlated with high temperature and low humidity. 13. The disease appeared 40 days after planting in the field and then it gradually increased reaching the peak by 90th day. 14. The pathogen was transmitted through tubers for two successive generations but to a lower percentage in the second generation. 15. Of the 36 cultivars/varieties of potato tested under field conditions, none were found to be resistant, However, the vars. JF 542, JF 4612, JG 676, JG 900, JC 750 and JE 812 had less than five per cent infection. Kufri Chandramukhi and Kufri Jyoti were highly susceptible having 48.3 and 47.6 per cent incidence, respectively. The highest average incidence of PTR in these cultivars in farmer’s fields was 35.85 and 26.03 per cent, respectively. 16. There was considerable loss in yield in many cvs. Viz., JC 750, BS/F 100, JC 182 and EM/F 2120. 17. The weight of tubers produced by the infected plants was always less than the tubers obtained from the adjacent healthy plants. The infected plants produced more number of smaller tubers which aggregated close to the main stem attached on short stolons. 18. Complete remission was obtained at 500, 1000 and 2000 ppm, incomplete remission at 100 and 250 ppm and no remission at 50 ppm of tetracycline given alternatively for 20 days.ThesisItem Open Access Studies on the phyllosticta leaf spot of ginger(Department of Plant Pathology, College of Horticulture, Vellanikkara, 1981) Premanathan, T; KAU; Peethambaran, C KLaboratory and field experiments of “The studies on the Phyllosticta leaf spot of ginger” were conducted at the College of Horticulture Campus, Vellanikkara during 1979-1981. The first visible symptom of the disease was observed as chlorotic specks. Fructification was more during the later stages of crop growth. The detailed study on the plant and environmental factors influencing the disease development in the field revealed that the average number of leaves per plant has a significant positive correlation with the disease intensity. Koch’s postulate and morphological studies proved that the pathogen causing the disease is Phyllosticta zingiberi Ramakr. Uninjured leaves and first three leaves, even after injury, failed to exhibit the symptoms on inoculation. Conidia germinated by putting forth single or double germtubes. Sucrose solution (1,000 ppm) supported faster and maximum spore germination and the bipolar germination noted was maximum in this solution. The fungus entered the leaf by direct penetration of epidermal cells without appressoria formation. The pycnidiospores and mycelia of the pathogen were found to survive even after seven months in soil under different depths and moisture conditions. The type Maran was found to be the least susceptible followed by Karakkal and Bajpai, whereas type Vengara was the most susceptible one. Out of the 12 fungicides tried, one per cent Bordeaux mixture and 2,000 ppm Bayer 5072 gave cent per cent inhibition of the fungal growth in both solid and liquid media. Antracol 2,000 ppm and panolil above 500 ppm in solid medium; bavistin 2,000 ppm and cuman above 500 ppm in liquid medium gave cent per cent inhibition of fungal growth. In the field trial cuman, was found to be the most effective fungicide in controlling the disease, followed by Bordeaux mixture and panolil. Maximum rhizome yield was noticed in cuman treated plots followed by Bordeaux mixture.ThesisItem Open Access Antibiotic producing and antagonistic microorganisms in the forest soils of Kerala(Department of Plant Pathology, College of Horticulture, Vellanikkara, 1988) Vinod, P B; KAU; Sukumara Varma, AThe antibiotic producing and antagonistic fungi, actinomycetes and bacteria in the evergreen forest soils of Ladysmith forest of Thariyode in Wynad, and Cheriyakanom forest of Thekkadi in Idukki districts of Kerala State were studied. The phanerogamic flore around the sites of soil sample collection in both localities were identified. The total microbial population was studied in relation to the depth of soil. The microbial population was maximum in the top layer and decreased with increase in depth of soil. The total microbial population was higher in Idukki and in both districts, population of bacteria was maximum followed by actinomycetes and fungi. A diversified group of fungi consisting, Mucor, Syncephalastrum, Trichoderma, Microascus, Cunningphamella, Absidia, Aspergillus, Penicillium, Talaromyces, Paecelomyces and Fusarium was present. Three types of actinomycetes viz. Streptomyces sp. with straight sporophores, flexuous sporophores and fascicled sporophores were present while four types of bacteria viz., B. subtilis. Bacillus sp. identical to B. subtilis, Bacillus sp. with small cell and fast growth in NA and Bacillus sp. with small cell and slow growth in NA were present. Antagonistic properties of the isolated were studied with the test organisms Pythium myriotylum, Phytophthora palmivora and Rhizoctonia soleni. Mucor sp. and Cunninchamella elegans showed intermingling and overgrowth with all the test organisms while Absidia corymbefera, Syncephalastrum racemosum, Aspergillus meleus, A. tarreus, Microascus cinereus and Fusarium oxysporum showed this character with P. myriotylum and P. palmivora. Intermingling and overgrowth character was observed in Paecelomyces lilacinus with P. palmivora and R. solani whereas A. versicolor and three species of streptomyces showed this character only with P. palmivora. Mutual inhibition on contact was exhibited by Talaromyces wortmannii with all the three test organisms, while A. versicolor and Streptomyces spp. with flexuous sporophores and fascicled sporophores showed this character with P. myriotylum and R. solani. This character was observed in case of A. corymbefera, S. racemosum, A. meleus, M. cinereus, F. oxysporum and Streptomyces sp. with straigtht sporophores, with R. solani while P. lilacinus showed this with P. myrootylum. Mutual inhibition at a distance was shown by Penicillium citrinum, P. simplicissimum, B. subtilis and the other three Bacillus spp. when tested with P. palmivora and R. solani, but A. terreus showed this reaction only with R. solani. Inhibition at a distance and disintegration of test organism was shown by A. niger with P. myriotylum and R. solani while P. citrinum and P. simplicissimum showed this character only with P. myriotylum. All the three spp. of Trichoderma showed die – back and disintegration of all the three test organisms, while A. niger showed this character only with P. palmivora and A. sydowii showed this character with R. solani only. streptomyces sp. with straight sporophores, B. subtilis and the other three Bacillus spp. showed this character with P. myriotylum alone. Inhibitory properties of antagonists using cell free culture filtrates were estimated and found that A. niger inhibited 100 per cent growth of all the three test organisms while P. citrinum, P. simpliciccimum and B. subtilis showed 100 per cent inhibition of P. myriotylum and a range of 67-87 per cent in case of P. palmovora and R. solani. A. terreus did not inhibit P. myriotylum and P. palmivora, but inhibites 78 per cent of R. solani. All the three Trichoderma spp. moderately inhibited all the three test organisms (13-26 per cent) while A. sydowii showed 20 per cent inhibition of R. solani only. Antibiotic property of the antagonists was determined and P. citrinum exhibited maximum, equivalent to 325 ppm tetracycline followed by Streptomyces with straight sporophores having 250 ppm. T. longibracheatum, P. simplicissimum and A. versicolor recovered antibiotic property equivalent to 150 ppm tetracycline hydrochloride while the other isolates had < 100 ppm equivalence of tetracycline hydrochloride.ThesisItem Open Access Management of sheath blight disease of rice in relation to the population of the pathogen in soil(Department of Plant Pathology, College of Horticulture, Vellanikkara, 1987) Shaji, Alexander; KAU; Rajan, K MLaboratory, pot and field experiments were carried out to study the role of various physical, chemical and biological factors on the management of sheath blight disease of rice caused by Rhizoctonia solani Kuhn. (Thanatephorus Cucumerlis (Frank) Donk). Populations of total fungi, bacteria and actinomycetes in soil were enumerated at different stages of growth of the crop in order to assess their role in reducing the intensity and incidence of sheath blight disease. Results of the investigation revealed that the pathogen can be managed by deeper ploughing followed by submergence of the soil for a minimum period of two months. Amendments like glyricidia leaves, rice husk, lime and non edible oil cakes of marotti, neem and punna were useful in reducing the severity and spread of the disease. Fungicides like carbendazim and ediphenphos and the herbicide benthiocarb were also efficient in managing the disease. Rotation of rice with crops like tapioca, banana and brinjal was also useful. It was seen that amendments stimulated the population of saprophytes like Trichoderma viride in soil which are antagonistic to R. solani resulting in a subsequent reduction in population of the pathogen. In spite of the reduction in severity and spread of the disease, grain and straw yields were not enhanced by the treatments. More elaborate field trials are to be undertaken before landing on any ultimate conclusion regarding the use of these practices as tools for disease management.