No abstract

The research was conducted to evaluate in-vitro efficacy of numerous fungicides against Fusarium oxysporum f. sp. capsici. In present research, six treatments (T) viz. Carbendazim, Benomyl, Topsin-M, Difenoconazole, Nativo, and Alliete along with control, various concentrations (C), days (D), and their interactions, i.e., (T × C), (T × D), (C × D), and (T × C × D) were exploited in a laboratory through food poison technique. Alliete expressed maximum colony growth (1.93 cm) as compared to all other fungicides with respect to control. Interaction between treatments and concentration (T × C) exhibited maximum colony growth of all treatments (Carbendazim, Benomyl, Topsin-M, Difenoconazole, Nativo, and Alliete), i.e., 0.87, 1.23, 1.73, 2.20, 2.53, and 2.93 cm at 300 ppm as compared to 500 and 700 ppm concentrations, respectively. Similar trend was also observed concerning interaction between (fungicides × days) and (tested concentrations × days). Results of the present study revealed that among tested fungicides, Carbendazim at 700 ppm expressed significant reduction in fungal growth.

The current research was conducted to find out the most appropriate concentrations of six fungicides for the management of sesame charcoal rot caused by Macrophomina phaseolina under lab and field conditions. The treatments viz. Antracol, Topsin-M, Mancozeb, Score, Topas, Nativo and Control with concentrations of 150, 250 and 350ppm were used with three replications under completely randomized design and randomized complete block design in Lab. and field conditions respectively. The mean colony growth of all treatments expressed that Nativo exhibited minimum colony growth of (0.93 cm) as compared to Score (1.14 cm), Topsin-M (1.42 cm), Mancozeb (1.77 cm), Antracol (2.04 cm), Topass (2.33 cm) correspondingly. The interaction between treatments and concentrations (T×C) showed that  used concentrations 150 ppm, 250 ppm and 350 ppm of Nativo abundantly inhibit fungal colony growth upto 1.26 cm, 0.86 cm and 0.66 cm respectively whereas the interaction between treatments and days expressed that after day ninth the minimum colony growth (1.23 cm) was observed for Nativo as compared to all other treatments. Similarly, the interaction between concentrations and days expressed highest fungal colony growth at concentration 150 ppm on day third (2.06 cm), sixth (3.02 cm) and ninth (3.65 cm) but the interaction of treatments, days and concentrations expressed that at 150 ppm concentration, all treatments exhibited minimum colony growth (1.70 to 3.30) cm at third, sixth and ninth day as compared to 250 and 350 ppm concentration respectively with respect to control (6.90 cm). In filed conditions, Nativo exhibited minimum Mean Disease Incidence (12.55%) whereas the interaction between treatments and days showed minimum of 14.95%, 12.82% and 9.90% disease incidence by Nativo as compared to all other treatments including control (66.86%, 77.57% and 87.22%) after day tenth, twenty and thirty. It was concluded that Nativo is significantly inhibiting the colony growth under lab and filed conditions.

Red cotton bug, Dysdercus koenigii (Hemiptera: Pyrrhocoridae), has become the major insect pest of various crops, including cotton, and thereby reducing the yield qualitatively and quantitatively and synthetic insecticides belonging to different groups are the major control agents for such insect pests. A laboratory experiment was carried out to evaluate the effect of different conventional insecticides, i.e., imidacloprid, deltamethrin, lambda cyhalothrin, gamma cyhalothrin and cyfluthirn on haemocytes of D. koenigii. The individuals were exposed to insecticides separately and data was recorded after 30 and 60 min of the exposure. The findings of current study depicted chlorpyrifos to be more effective and significant alterations in total haemocyte counts and differential haemocyte counts were observed in the cyfluthirn treated D. koenigii. In addition to this, cell structure was also disrupted as an immune response. Similar studies would also be helpful to understand the defence mechanisms of insects against the xenobiotics which will help to device efficient management tools for D. koenigii.