Experiment code 12091-2-1
Experiment Title Management of mango Malformation
Research Type Departmental Research
Experiment Background Mango (Mangifera indica L.) is very important fruit crop of India and ranks 1st in world mango production with production of 22 Million Tones in 2019. The fungal, bacterial, viral and nematode diseases play major role in the decline of mango fruit yield and fruit quality. Among them anthracnose, mango malformation, powdery mildew, stem end rot are recorded major disease from nursery to harvesting of fruits or storage conditions. Malformation is the most threatening malady that causes great economic loss and limits the mango production in India and among tropical and subtropical countries around the globe. Floral malformation, in contrast to vegetative one, is very virulent and can cause the loss of the entire crop. Keeping this in mind the present study will be carried out to study the effectiveness different module against malformation in mango.
Experiment Group Plant Protection
Unit Type (01)RESEARCH UNIT
Unit (58)AGRICULTURE EXPERIMENTAL STATION (PARIA)
Department (284)Agriculture Experimental Station Paria
BudgetHead (325/12091/02)325/07/REG/02125
Objective

To find out effective management module for management of mango malformation

Season Perennial
Location Unit Type (01)RESEARCH UNIT
Location Unit (58)AGRICULTURE EXPERIMENTAL STATION (PARIA)
Location Department (284)Agriculture Experimental Station Paria
Plot No Farmer field
PI Name (NAU-EMP-2011-000786)NIRAV KRUSHNAKANT GAJRE
PI Email niravgajre@nau.in
PI Mobile 9998860728
Year of Approval 2015
Commencement Year 2016
Completion Year 2022
Design of Experiment

 RBD

Crop Spacing (cm x cm)

8 m x 8 m

Gross Plot (m x m) NA
Net Plot (m x m) NA
Total Experiment Area (m2) 3200 m2
Plot History Last Three Year

NA

Initial Soil Sample Analysis Report

NA

Initial Soil Sample Analysis Report Attachment Attachment Not Available!
Layout Plan

NA

Layout Plan Attachment Attachment Not Available!
Treatment

Module-1

: Spray of Copper oxychloride 0.3%, at the time of

vegetative flush, subsequent spray Carbendazim 0.1%

at 20 days after first spray + Spray Propargite 0.18% at

20 days after second spray + Spraying 200 ppm NAA

in second week of December followed by spraying of

500 ppm etherel at bud inception stage.

Module-2

Spraying 1000 ppm paclobutrazol in first week of

October, followed by spray of Copper oxychloride

0.3%, subsequent spray Carbendazim 0.1% at 20 days

after first spray, Spray Propargite 0.18% at 20 days

after second spray, Spraying 100 ppm GA3 at bud

inception stage.

Module-3

Spray of Trichoderma viride (NAU Isolate) 106

spores/ml, at initiation of vegetative flush, subsequent

spray T. harzianum (NAU Isolate) 106 spores/ml. 20

days after first spray, spray Pseudomonas florescence

(NAU) 108 CFU, 20 days after second spray, spray

Baccilus subtilis (NAU) 108 at the time of flower bud

initiation

Module-4

Existing practices removal of affected panicle and

pasting of copper oxychloride

Module-5

Control (Un treated)

Treatment Attachment Attachment Not Available!
(NAU-EMP-2011-000786) NIRAV KRUSHNAKANT GAJRE niravgajre@nau.in 9998860728 04-12-2021
Active
(NAU-EMP-2006-000796) SAGAR JANARDAN PATIL goldmedalist@nau.in 9998012218 04/12/2021
Active
(NAU-EMP-2015-000798) SANDEEPKUMAR GAUTAMBHAI PARMAR sgparmar@nau.in 9898245830 04/12/2021
Active
Mango Kesar