2016
DOI: 10.21162/pakjas/16.4861
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HISTOPATHOLOGICAL CHANGES IN RESPONSE TO Ceratocystis manginecans IN MANGO (Mangifera indica)

Abstract: Ceratocystis manginecans is a destructive systemic fungus and a major cause of mango sudden decline. Heavy losses to the mango industry in Pakistan are due to this disease. This study was designed to evaluate the histological changes in mango seedlings inoculated with C. manginecans. The pathogenic fungus was inoculated to indigenous mango germplasm of Punjab, Azad Jammu and Kashmir. After one week of inoculation, plants started showing disease symptoms including gum exudation, wilting of leaves, discoloration… Show more

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Cited by 3 publications
(3 citation statements)
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“…The general conclusion is that frequent and timely application of fungicides can ensure convincing control of blossom diseases and high yields. The results of this particular study are in general agreement with those of several investigators (Haq et al, 1994;Akhtar et al, 1998;Ihsan et al, 1999;Guizen et al, 2003;Anjum et al, 2016). Table 2.…”
Section: Effectiveness Of Chemicals On Blossom Diseasessupporting
confidence: 92%
“…The general conclusion is that frequent and timely application of fungicides can ensure convincing control of blossom diseases and high yields. The results of this particular study are in general agreement with those of several investigators (Haq et al, 1994;Akhtar et al, 1998;Ihsan et al, 1999;Guizen et al, 2003;Anjum et al, 2016). Table 2.…”
Section: Effectiveness Of Chemicals On Blossom Diseasessupporting
confidence: 92%
“…For histopathological studies, 10 mm transverse slices of stems and roots of healthy and diseased tomato plants were preserved in Formalin acetic acid (acetic acid 5%, v/v formalin 10%, distilled water 35% and ethyl alcohol 50%) for the 48 hours (Anjum et al, 2016). For long term storage, fixed samples were then transferred to Acetic ethanol solution (ethanol 75% and v/v acetic acid 25%).…”
Section: Histopathological Studiesmentioning
confidence: 99%
“…Fixed stems and roots were sectioned into 3mm transvers portions by freehand sectioning. To prepare permanent slides, the sections were dehydrated through the serial dilutions of ethanol and stained using standard double-staining technique of safranine and fast green stains (Anjum et al, 2016). Real time images were taken with microscope camera after observing under OMAX microscope model G017075953.…”
Section: Histopathological Studiesmentioning
confidence: 99%