Indian Journal of Agricultural Research

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Indian Journal of Agricultural Research, volume 57 issue 2 (april 2023) : 235-241

Integrated Management of Stem Rot of Groundnut Caused by Sclerotium rolfsii. sacc

G. Narendra Babu1,*, D. Sandhya Deepika2
1College of Science and Technology Andhra University, Visakhapatnam-530 003, Andhra Pradesh, India.
2Department of Botany, College of Science and Technology Andhra University, Visakhapatnam-530 003, Andhra Pradesh, India.
Cite article:- Babu Narendra G., Deepika Sandhya D. (2023). Integrated Management of Stem Rot of Groundnut Caused by Sclerotium rolfsii. sacc . Indian Journal of Agricultural Research. 57(2): 235-241. doi: 10.18805/IJARe.A-6043.
Background: Groundnut is the principal vegetable oil crop in India and about 85 per cent groundnut area under remains rain fed. Stem rot of groundnut is more prevalent in the area and is capable of causing considerable loss in the yield when left unmanaged.

Methods: In order to find out an effective method of managing the disease, an integrated approach was adopted by combining the use of bio agents, organic amendments and fungicides alone and in combinations.
 
Result:
Seed treatment with tebuconazole @ 1 g kg-1 and with commercial formulation of Trichoderma harzianum @ 5g kg-1 seed along with soil application of neem cake @ 1.3 t ha-1 maintained its superiority over other treatments by recording the least PDI, maximum germination percentage (98.20%), root length (14.62 cm), shoot length (35.54 cm), number of pods per plant (32.57) and pod yield (3920.0 kg ha-1) which may be synergistic effect of organic amendment with bioagent. However, all the sole treatments also managed the disease to some extent but greater control was recorded in combination treatments than alone.
Groundnut (Arachis hypogea L.) is one of the most important oilseed crop in the world and the largest producer being China followed by India, Nigeria and United States (Groundnut Outlook, Agricultural Market Intelligence Centre, PJTSAU, 2019). Groundnut crop is affected with various diseases caused by fungi, bacteria, nematodes and viruses which reduce the pod yield of groundnut and also the fodder quality of haulm. Among the fungal diseases, stem rot caused by Sclerotium rolfsii Sacc, is one of the major constraints in groundnut production as it severely affects the yield and quality of the produce. It is one of the most economically important diseases of groundnut which accounts for 10 to 25 per cent loss in yield annually (Sturgeon, 1986). It was first observed by Peter Henry Rolfs in the year 1892 on tomato plants with 70% losses. The hyphae grew upward on the surface of the infected plant covered with a cottony, white mass of mycelium, scattered inside and outside of infected stem nearby the soil surface, The fungus produced numerous small round, white sclerotia of uniform size when immature and dark brown at mature stage (Kwon and Park, 2002). In India, stem rot incidence is most severe in Maharashtra, Gujarat, Madhya Pradesh, Karnataka andhra Pradesh, Odisha and Tamil Nadu, This disease causes severe damage and can reach over 80% in heavily infected fields (Mehan and McDonald, 1990).

The management of seed and soil-borne diseases only by seed treatment has been practical as soil application of chemicals has not only been expensive but also not practical. Thus other alternative disease management options were considered and among which biological control appear promising and have been considered as environmentally safe and virtuous supplement to the synthetic fungicides (Abada and Ahmad, 2014; Sohaliya et al., 2019). Various reports show the widespread application of Trichoderma spp. such as T. asperellum, T. atroviride, T. gamsii, T. hamatum, T. harzianum, T. polysporum, T. virens and T. koningii as bio control agents effective against various soil-borne pathogens such as Phytophthora, Pythium, Aspergillus, Fusarium and Rhizoctonia [(Moosa et al., 2017; Javaid et al., 2018; Sharma and Prasad 2018; Ingale and Patale (2019)] and organic amendments to suppress soil borne pathogens (Bonanomi et al., 2018). Several studies also suggest that when the bacterial or fungal antagonists such as P. flourescens or Trichoderma spp. were used in combination with organic amendments, their antagonistic efficacy was enhanced (Karthikeyan et al., 2006; Vengadeshkumar et al., 2019; Jangir et al., 2020). Organic amendments induce the association of beneficial micro flora around the rhizosphere, which can be of help to reduce the plant pathogens in the soil (Tayyab et al., 2019). Therefore, an attempt was made to identify the best biocontrol agent for the management of Sclerotium rolfsii the causal agent of stem rot of groundnut by evaluating seed treatment with chemical, bioagent and application of neem cake and their combinations in field during rabi, 2020-2021.
The field experiments were laid out in sandy loamy soils having good drainage facility at Chinthalapalem village, Darsi mandal, Prakasam district during rabi, 2020 and 2021 under irrigated dry conditions. Recommended doses of nitrogen, phosphorus and potassium (20-40-40) kg ha-1 were applied in the form of urea, single super phosphate and muriate of potash respectively. The groundnut variety ‘K-6’ with duration of 105-110 days was selected for the study and sown with a spacing of 22.5×10 cm in plots of 5×3 m. All packages of practices recommended for groundnut was followed. Randomised Block Design was adopted with eight treatments viz., T1- Seed treatment with tebuconazole @1 g kg-1 ; T2- Seed treatment with T. harzianum @ 5 g kg-1 seed; T3- Soil application of neem cake @ 1.3 t/ha; T4- Seed treatment with tebuconazole @ 1 g kg-1  + T. harzianum @ 5g kg-1 seed; T5- Seed treatment with tebuconazole @ 1g kg-1 seed + soil application of neem cake @ 1.3t/ha; T6- Seed treatment with tebuconazole @ 1 g kg-1 + T. harzianum @ 5 g kg-1 seed + soil application of neem cake @ 1.3t/ha; T7- Seed treatment with T. harzianum @ 5 g kg-1 seed + neem cake @ 1.3 t/ha and T8 as control plot with three replications.

The observations recorded during field study are percent seed germination, percent disease incidence @ 45 DAS, 60 DAS and 75 DAS, shoot length, root length, number of pods per plant, pod yield and Area Under Disease Progress Curve (AUDPC).
AUDPC was calculated using the formula:
 
 
Where,
n = Total number of observation.
yi = Disease incidence recorded at the ith observation.
ti  = Time at the ith observation. 

The data obtained in the present investigation was analysed statistically using RBD and presented.
During rabi, 2020-21
 
Germination percentage
 
Among the 8 treatments imposed, T6 i.e., seed treatment with tebuconazole @ 1 g kg-1 seed (ST) + T. harzianum @ 5 g kg-1 + soil application of neem cake @ 1.3 t/ha recorded significantly higher germination percentage (97.9%) followed by T4 (seed treatment with tebuconazole 1 g and T. harzianum @ 5 g kg-1 seed) (96.3%). The least germination percentage (83.7%) has been recorded in T8 (control) (Table 1).

Table 1: Effect of various treatments on germination percentage and percent disease incidence under field conditions during rabi, 2020-21.



Per cent disease Incidence
 
At 45 DAS, highest percent disease incidence (11.49%) among the treatments was recorded with T(soil application of neem cake @ 1.3 t/ha) which was on par with T2 (seed treatment with T. harzianum @ 5 g kg-1) (11.29%). Least PDI (3.50%) was observed in T6 (seed treatment with tebuconazole @ 1g kg-1 seed + T. harzianum @ 5 g kg-1 + soil application of neem cake @ 1.3 t/ha) followed by T5 (seed treatment with tebuconazole 1 g kg-1 + soil application of neem cake @ 1.3t/ha) which recorded a PDI of 7.62 per cent and 17.99 PDI has been recorded in T8 (control) (Table 1).

At 60 DAS, T3 (soil application of neem cake @ 1.3t/ha) recorded the maximum PDI of 22.98 per cent while T6 (seed treatment with tebuconazole @ 1 g kg-1 seed + T. harzianum @ 5 g kg-1 seed + soil application of neem cake @ 1.3t/ha) was recorded minimum disease incidence (10.57%) followed by T7 (seed treatment with T. harzianum @ 5g kg-1 + soil application of neem cake @ 1.3 t/ha) which recorded 14.02%  and 28.93% PDI was recorded in control plot (T8) (Table 1).

At 75 DAS, T3 (soil application of neem cake @ 1.3t/ha) recorded the maximum PDI of 24.87 per cent while Least PDI was observed in T6 i.e., seed treatment with tebuconazole @ 1g kg-1 seed + T. harzianum @ 5g kg-1 seed + soil application of neem cake @ 1.3t/ha (13.38%) and 32.88% PDI was recorded in control plot (T8) (Table 1).
 
Area under disease progress curve (AUDPC)
 
The AUDPC for various treatments was calculated. T8 (control) recorded highest AUDPC (765.67) while T6 recorded the least (176.08). Among the individual treatments the descending order of AUDPC is T3 (537.65) > T2 (443.19) > T1 (424.44). Among the combination treatments, AUDPC of T7 (380.45) > T4 (363.97) > T5 (350.17) > T6 (176.08) (Table 1).
 
Root length and shoot length
 
Maximum root and shoot length (14.52 cm and 35.74 cm) was recorded in T6 (seed treatment with tebuconazole @ 1 g kg-1 seed + T. harzianum @ 5 g kg-1 seed + soil application of neem cake @ 1.3 t/ha) followed by T5 (seed treatment with tebuconazole @ 1g kg-1 seed + soil application of neem cake @ 1.3 t/ha) which recorded a root and shoot length of 12.73 cm and 32.27 cm respectively, while the least root and shoot length (8.66 cm and 20.43 cm) was recorded in T8 (control) (Table 2).

Table 2: Effect of various treatments on root and shoot length, number of pods per plant and pod yield under field conditions during rabi, 2020-21.


 
No of pods per plant and pod yield
 
Highest number of pods per plant (32.40) was observed in the treatment T6 (seed treatment with tebuconazole @ 1 g kg-1 seed +T. harzianum @ 5 g kg-1 seed + soil application of neem cake @ 1.3 t/ha) followed by T7 (seed treatment with T. harzianum @ 5 g kg-1 seed + soil application of neem cake @ 1.3 t/ha) where the number of pods per plant was 26.00. Least number of pods per plant (13.00) was observed in the control (T8). Maximum pod yield (3873.33 kg ha-1) with highest benefit cost ratio of 4.54 was recorded with the treatment T6 (seed treatment with tebuconazole @ 1 g kg-1 seed + T. harzianum @ 5g kg-1 seed + soil application of neem cake @ 1.3t/ha) followed by T7 (seed treatment with T. harzianum @ 5g kg-1 seed + soil application of neem cake @ 1.3t/ha) which recorded a yield of 3150.0 kg ha-1 with 3.72 benefit cost ratio, whereas T8 (control) had the least yield (1240.0 kg ha-1) (Table 2).
 
During rabi, 2021-22
 
Germination percentage
 
Among the 8 treatments imposed, T6 i.e., seed treatment with tebuconazole @ 1 g kg-1 seed (ST) + T. harzianum @ 5 g kg-1 + soil application of neem cake @ 1.3 t/ha recorded significantly higher germination percentage (98.5%) followed by T4 (seed treatment with tebuconazole 1 g and T. harzianum @ 5g kg-1 seed) (96.9%). The least germination percentage (82.9%) has been recorded in T8 (control) (Table 3).

Table 3: Effect of various treatments on germination percentage and per cent disease incidence under field conditions during rabi, 2021-22.


 
Per cent disease Incidence
 
At 45 DAS, highest percent disease incidence (11.80%) among the treatments was recorded with T3 (soil application of neem cake @ 1.3 t/ha) which was on par with T2 (seed treatment with T. harzianum @ 5 g kg-1) (11.01%). Least PDI (3.10%) was observed in T6 (seed treatment with tebuconazole @ 1 g kg-1 seed + T. harzianum @ 5 g kg-1 + soil application of neem cake @ 1.3 t/ha) followed by T4 (seed treatment with tebuconazole 1g and T. harzianum @ 5 g kg-1) which recorded a PDI of 7.61 per cent and 20.07% PDI was recorded in control plot (T8) (Table 3).

At 60 DAS, T6 (seed treatment with tebuconazole @ 1 g kg-1 seed + T. harzianum @ 5 g kg-1 seed + soil application of neem cake @ 1.3 t/ha) recorded minimum disease incidence (9.78%) followed by T5 (seed treatment with tebuconazole @ 1g kg-1 seed + soil application of neem cake @ 1.3 t/ha) which recorded 14.32% and 30.44% PDI was recorded in control plot (T8) (Table 3).

At 75 DAS, T3 (soil application of neem cake @ 1.3 t/ha) recorded the maximum PDI of 24.87 percent while Least PDI was observed in Ti.e., seed treatment with tebuconazole @ 1 g kg-1 seed + T. harzianum @ 5 g kg-1 seed + soil application of neem cake @ 1.3 t/ha (13.04%) followed by T7 (seed treatment with T. harzianum @ 5 g kg-1 seed + soil application of neem cake @ 1.3 t/ha) which recorded (14.62%) and 36.15% PDI was recorded in control plot (T8) (Table 3).
 
Area under disease progress curve (AUDPC)
 
The AUDPC for various treatments was calculated. T8 (control) recorded highest AUDPC (854.28) while T6 recorded the least (217.05). Among the individual treatments the descending order of AUDPC is T3 (576.70) > T2 (480.08) > T(454.15) and among combination treatments, the descending order of AUDPC is T7 (393.79) > T5 (388.18) > T4 (376.00) > T6 (217.05) (Table 3).
 
Root length and shoot length
 
Maximum root and shoot length (14.71 cm, 35.33 cm) was recorded in T6 (seed treatment with tebuconazole @ 1g kg-1 seed + T. harzianum @ 5 g kg-1 seed + soil application of neem cake @ 1.3 t/ha) followed by T5 (seed treatment with tebuconazole @ 1 g kg-1 seed + soil application of neem cake @ 1.3 t/ha) which recorded a root and shoot length of 13.40 cm and 32.37 cm respectively, while the least root and shoot length (8.79 cm and 20.17 cm) was recorded in T8 (control) (Table 4).

Table 4: Effect of various treatments on root and shoot length, number of pods per plant and pod yield under field conditions during rabi, 2021-22.


 
No of pods per plant and pod yield
 
Highest number of pods per plant (32.73) was observed in the treatment T6 (seed treatment with tebuconazole @ 1g kg-1 seed +T. harzianum @ 5g kg-1 seed + soil application of neem cake @ 1.3 t/ha) followed by T7 (seed treatment with T. harzianum @ 5 g kg-1 seed + soil application of neem cake @ 1.3 t/ha) where the number of pods per plant was 24.67. Least number of pods per plant (12.33) was observed in the control (T8). Maximum pod yield (3966.67 kg ha-1) with highest benefit cost ratio of 4.60 was recorded with the treatment T6 (seed treatment with tebuconazole @ 1 g kg-1 seed + T. harzianum @ 5 g kg-1 seed + soil application of neem cake @ 1.3 t/ha) followed by T7 (seed treatment with T. harzianum @ 5 g kg-1 seed + soil application of neem cake @ 1.3 t/ha) which recorded a yield of 3076.67 kg ha-1 with 3.68 benefit cost ratio, whereas T8 (control) had the least yield (1236.67 kg ha-1) with 1.98 benefit cost ratio (Table 4).
 
Pooled data (Rabi, 2020-21 and 2021-22)
 
Germination percentage
 
Treatment T6 i.e., seed treatment with tebuconazole @ 1g kg-1 seed (ST) + T. harzianum @ 5g kg-1 + soil application of neem cake @ 1.3 t/ha recorded significantly higher germination percentage (98.2%) followed by T4 (seed treatment with tebuconazole 1 g and T. harzianum @ 5 g kg-1 seed) (96.6%). The least germination percentage (83.33%) has been recorded in T8 (control) (Table 5).

Table 5: Pooled data of effect of various treatments on germination percentage and per cent disease incidence under field conditions.



Per cent disease Incidence
 
At 45 DAS, highest per cent disease incidence (16.80%) among the treatments was recorded with T2 (seed treatment with T. harzianum @ 5 g kg-1) which was on par with T3 (soil application of neem cake @ 1.3 t/ha) (17.39%). Least PDI (5.05%) was observed in T6 (seed treatment with tebuconazole @ 1 g kg-1 seed + T. harzianum @ 5 g kg-1 + soil application of neem cake @ 1.3 t/ha) followed by T5 (seed treatment with tebuconazole @ 1 g kg-1 seed + soil application of neem cake @ 1.3 t/ha) which recorded a PDI of 11.53 per cent (Table 5).

At 60 DAS, T6 (seed treatment with tebuconazole @ 1g kg-1 seed + T. harzianum @ 5 g kg-1 seed + soil application of neem cake @ 1.3 t/ha) recorded minimum disease incidence (15.46%) followed by T7 (seed treatment with T. harzianum @ 5 g kg-1+ soil application of neem cake @ 1.3 t/ha) which recorded 21.85% (Table 5).

At 75 DAS, T3 (soil application of neem cake @ 1.3 t/ha) recorded the maximum PDI of 37.30 per cent while Least PDI was observed in Ti.e., seed treatment with tebuconazole @ 1 g kg-1 seed + T. harzianum @ 5 g kg-1 seed + soil application of neem cake @ 1.3 t/ha (19.90%). At 75 DAS, maximum PDI was recorded in control plot (T8) with 50.96% (Table 5).
 
Area under disease progress curve (AUDPC)
 
The AUDPC for various treatments was calculated. T8 (control) recorded highest AUDPC (1213.35) while T6 recorded the least (343.24). Among the individual treatments the descending order of AUDPC is T3 (855.53) > T2 (742.84) > T(665.40) and among combination treatments, the descending order of AUDPC is T5 (580.88) > T4 (576.60) > T7 (573.86) > T6 (343.24) (Table 5).

Root length and shoot length
 
Maximum root and shoot length (14.62 cm, 35.54 cm) was recorded in T6 (seed treatment with tebuconazole @ 1 g kg-1 seed + T. harzianum @ 5g kg-1 seed + soil application of neem cake @ 1.3 t/ha) followed by T5 (seed treatment with tebuconazole @ 1 g kg-1 seed + soil application of neem cake @ 1.3 t/ha) which recorded a root and shoot length of 13.07 cm and 32.32 cm respectively, while the least root and shoot length (8.72 cm and 20.30 cm) was recorded in T8 (control) (Table 6).
 
No of pods per plant and pod yield
 
Highest number of pods per plant (32.57) was observed in the treatment T6 (seed treatment with tebuconazole @ 1 g kg-1 seed +T. harzianum @ 5g kg-1 seed + soil application of neem cake @ 1.3 t/ha) followed by T7 (seed treatment with T. harzianum @ 5 g kg-1 seed + soil application of neem cake @ 1.3 t/ha) where the number of pods per plant was 25.33. Least number of pods per plant (12.67) was observed in the control (T8). Maximum pod yield (3920.0 kg ha-1) with highest benefit cost ratio of 4.57 was recorded with the treatment T6 (seed treatment with tebuconazole @ 1 g kg-1 seed + T. harzianum @ 5g kg-1 seed + soil application of neem cake @ 1.3 t/ha) followed by T7 (seed treatment with T. harzianum @ 5 g kg-1 seed + soil application of neem cake @ 1.3 t/ha) which recorded a yield of 3113.3 kg ha-1 with 3.70 benefit cost ratio, whereas T8 (control) had the least yield (1238.3 kg ha-1). This may be due to the synergistic effect of chemical control by fungicide along with the use of bio agent and organic amendment. The findings are in agreement with several studies (Sindhu keerthana et al., 2022; Karthikeyan et al., 2006; Manjunatha et al., 2011; Nageswararao et al., 2012; Kumar et al., 2015; Choudhary and Ashraf, 2019 and Gaikwad et al., 2020) which reported enhanced disease control of dry root rot and stem rot in groundnut when organic amendments, fungicides and bio agents were integrated. Also the results of studies conducted by various workers on different crops (Latha et al., 2017 in black gram, Thilagavathi et al., 2007 in green gram, Rajkumar et al., 2019; Manjunatha et al., 2011 and Deepa et al., 2018 in chickpea, Dhawan et al., 2019  in soybean, Adhikary et al., 2019 in sesame) for the management of R. bataticola have indicated that the integration of chemical, biological and organic measures not only has provided better control of the disease but also enhanced the crop growth and yield when compared to the use of only one of the management measures. (Table 6).

Table 6: Pooled data of effect of various treatments on root and shoot length, number of pods per plant and pod yield under field conditions.

Although reduction in disease appearance was recorded in individual treatments with fungicide, bio agents or organic amendments but greater disease control was recorded in treatments combining fungicide and bio agent or bio agent and organic amendment. The PDI was lowest in combination treatments when compared to sole treatments involving only fungicide, bio agent or organic amendment. The same pattern was observed with root length, shoot length, number of pods/plant and pod yield. Overall results indicate that seed treatment with T. harzianum @ 5 g kg-1+ soil application of neem cake @ 1.3 t/ha) was superior to all the treatments. It is also recorded highest maximum germination percentage- initial plant population (98.20%), root length (14.62 cm), shoot length (35.54 cm), highest number of pods per plant (32.57), pod yields (3920.0 kg ha-1) and least disease incidence (19.90%) which was a more than two fold decrease when compared to the control (50.96%). All these factors contributed to the almost three fold increase of yield in seed treatment with T. harzianum @ 5 g kg-1+ soil application of neem cake @ 1.3 t/ha)  when compared to the control with highest benefit cost ratio (4.57). The efficacy of all the three management inputs revealed that treatments involving integration of the inputs performed better in controlling the disease as well as in increasing the yield than imposing individually. Therefore, it can be concluded that integration of cultural, biological and chemical disease management practices not only exerts a synergistic effect on the disease control and also enhances the yield.
None

  1. Abada, M. and Ahmad, M. (2014). A comparative study for the effect of green tea extract and some antioxidants on Thompson seedless grapevines. Int J. Plant and Soil Sci. 3(10): 1333-1342. 

  2. Annonymus. (2019). Groundnut Outlook, May 2019. Agricultural Market Intelligence Centre (AMIC). PJTSAU. pp. 1-3.

  3. Adhikary, N.K., Chowdhury, R., Begum, T. and Mallick, R. (2019). Integrated management of stem and root rot of sesame (Sesamum indicum L.) caused by Macrophomina phaseolina (Tassi) Goid. International Journal of Current Microbiology and Applied Sciences. 8(4): 804-808.

  4. Bonanomi, G., Lorito, M., Vinale, F. and Woo, S.L. (2018). Organic amendments, beneficial microbes and soil microbiota: Towards a unified framework for disease suppression. Annual Reviews of Phytopathology. 56: 1-20.

  5. Choudhary, A. and Ashraf, S. (2019). Utilizing the combined antifungal  potential of Trichoderma spp. and organic amendments against dry root rot of mungbean. Egyptian Journal of Biological Pest Control. 29: 83. (2019). https://doi.org/ 10.1186/s41938-019-0187-8.

  6. Deepa, Sunkad, G., Sharma, M., Mallesh, S.B., Mannur, D.M. and Sreenivas, A.G. (2018). Integrated management of dry root rot caused by Rhizoctonia bataticola in chickpea. International Journal of Current Microbiology and Applied Sciences. 7(4): 201-209.

  7. Dhawan, A., Kumar, S., Sharma, P.K. and Chugh, R.K. (2019). Effect of different fungicides, organic amendments and bio-control agents on dry root rot of cluster bean [Cyamopsis  tetragonoloba (L.) Taub] caused by Rhizoctonia bataticola (Taub.) Butler. Forage Research. 44(4): 276-281.

  8. Gaikwad, P.A., Dhutraj, D.N., Ambadkar, S.V. and Navgire, K.D. (2020). Integrated disease management of Rhizoctonia bataticola causing dry root rot of chickpea. Journal of Pharmacognosy and Phytochemistry. 2020: 9(4): 3302-3306.

  9. Ingale and Patale. (2019). Antagonistic potential of Trichoderma sp. against fungal pathogens of pulses. A Quarterly Journal of Life Sciences. 16(4): 251-252.  

  10. Jangir, M., Sharma, S. and Satyawati, S. (2020). Synergistic effect of oilseed cake and biocontrol agent in the suppression of Fusarium wilt in Solanum lycopersicum. Brazilian Journal of Microbiology. 51: 1929-1939. 

  11. Javaid, A., Khan, A.I.H.  and Shoaib (2018). Management of charcoal  rot of mungbean by two Trichoderma species and dry biomass of Coronopus didymus. Planta Danin. 36: 1-8.

  12. Karthikeyan, V., Sankaralingam, A. and Nakkeeran, S. (2006). Management of groundnut root rot with biocontrol agents and organic amendments. Archives of Phytopathology and Plant Protection. 39(3): 215-223.

  13. Kumar, P., Gaur, V.K. and Rani, R. (2015). Evaluation of antagonists against Macrophomina phaseolina causing root rot in groundnut. African Journal of Microbiology Research. 9(3): 155-160.

  14. Kwon and Park (2002). Stem rot of tomato caused by Sclerotium rolfsii in Korea. Mycobiology. 30(4): 244-246.

  15. Latha, P., Karthikeyan, M. and Rajeswari, E. (2017). Development of bioformulations for the management of blackgram dry root rot caused by Rhizoctonia bataticola (Taub.) butler. Advances in Research. 9(4): 1-12.

  16. Manjunatha, S.V., Naik, M.K., Patil, M.B and Rani, G.S.D. (2011). Biological control of dry root rot of chickpea caused by Rhizoctonia bataticola (Taub) Butler. Journal of Mycopathological  Research. 49(1): 127-130. 

  17. Mehan, V.K. and McDonald, D. (1990). Some important diseases of groundnut-sources of resistance and their utilization in crop improvement. Paper presented at the in Country Training Course on Legumes Production. July 9-17, Sri Lanka. limited distribution. 

  18. Moosa, A., Sahi, ST., Haq, IU., Farzand, A., Khan, SA., Javaid, K. (2017). Antagonistic potential of Trichoderma isolates and manures against Fusarium wilt of tomato. Int J. Vegetable Sci. 23(3): 207-218.

  19. Nageswararao, G., Patibanda, A. K and Ranganathswamy, M. (2012). Studies on the efficacy of fungicides, organic amendments and biocontrol agent on dry root rot (Rhizoctonia bataticola)  of groundnut in vivo. Journal of Mycopathological Research. 50(2): 285-289.

  20. Rajkumar, S., Srinivas, T., Kumari V. and Kumar, D.V.S.R.P. (2019). Integrated management of dry root rot [Rhizoctonia bataticola (Taub,) butler] of chickpea. International Journal of Plant Sciences. 14(1): 1-9.

  21. Sharma, K.S. and Prasad. L. (2018). Bioactivity of Trichoderma asperellum against Colletotri chum asianum and Sclerotinia  sclerotiorum. Pest Res J. 30: 251-255.

  22. Sindhu Keerthana, Y., Srinivas, T., Devi, R.S.J. and SriVidhya, A. (2022). Integrated management of dry root rot of Arachis hypogaea caused by Rhizoctonia bataticola. Research on Crops. 23(2): 453-457. 

  23. Sohaliya, N.N., Pathak, D.M., Pandya, J.R. (2019). In vitro antagonistic  activity of Trichoderma species against important soil borne pathogens. Intl J. Plant Prot. 12: 127-131.

  24. Sturgeon, R.V.J. (1986). Peanut disease loss estimates for major peanut producing states in the United States for 1984 and 198.5. Proc. Amer. Peanut Science (2003) 30: 128- 133 Peanut Res. Educ. Soc. 18: 24-25.

  25. Tayyab, M., Islam, W., Lee, C.G., Pang, Z., Khalil, F., Lin, S., Lin, W. and Zhang, H. (2019). Short-term effects of different organic amendments on soil fungal composition. Sustainability. 11(198): 1-13.

  26. Thilagavathi, R., Saravanakumar, D., Ragupathi, N. and Samiyappan,  R. (2007). A combination of biocontrol agents improves the management of dry root rot (Macrophomina phaseolina)  in greengram. Phytopathologia Mediterranea. 46: 157-167.

  27. Vengadesh Kumar, L., Kalaiselvi, M., Meera, T., Sanjayghandi, S., Udhayakumar, R., Rajamohan, K. and Sudhasha, S. (2019). Effect of neem compared with Pseudomonas fluorescens on the management of cowpea root rot disease. Journal of Biopesticides. 12(2): 232-238.

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