- Author: Surendra K. Dara
Botrytis fruit rot or gray mold, caused by Botrytis cinerea, is common fruit disease in California strawberries (Koike et al. 2018). Botrytis cinerea has a wide host range infecting several commercially important crops including blueberry (Saito et al. 2016), grapes (Saito et al., 2019), and tomato (Breeze, 2019). Fungal infection can cause flower or fruit rot. Fruit can be infected directly or through a latent infection in the flowers. Moist and cool conditions favor fungal infections and increased sugar content in the ripening fruit can also contribute to the disease development. Initial symptoms of infection appear as brown lesions and a thick mat of gray conidia is characteristic symptom in the later stages of infection. As chemical fungicides are primarily used for gray mold control, fungicide resistance is a common problem around the world (Panebianco et al., 2015; Liu et al., 2016; Stockwell et al., 2018; Weber and Hahn, 2019). In strawberry, cultural control options such as removing diseased plant material or using cultivars with traits that can reduce gray mold infections may not be practical when the disease is widespread in the field or cultivar choice is made based on other factors. Non-chemical control options are necessary to help reduce the risk of chemical fungicide resistance, prolong the life of available chemical fungicides, achieve desired disease control, and to maintain environmental health. Although there are several botanical and microbial fungicides available for gray mold control, limited information is available on their efficacy in California strawberries. A study was conducted in the spring of 2019 to evaluate the efficacy of several chemical, botanical, and microbial fungicides in certain combinations and rotations to help identify effective options for an integrated disease management strategy.
Methodology
Strawberry cultivar San Andreas was planted late November, 2018 and the study was conducted in April and May, 2019. Each treatment had a 20' long strawberry plot with two rows of plants replicated in a randomized complete block design. Plots were maintained without any fungicidal applications until the study was initiated. Table 1 contains the list of treatments, application rates and dates of application, and Table 2 contains the type of fungicide used and their mode of action. Beauveria bassiana and Metarhizium anisopliae s.l. are California isolates of entomopathogenic fungi, isolated from an insect and a soil sample, respectively. These fungi are pathogenic to a variety of arthropods and some strains are formulated as biopesticides for arthropod control. However, earlier studies in California demonstrated that these fungi are also known to antagonize plant pathogens such as Fusarium oxysporum f.sp. vasinfectum Race 4 (Dara et al., 2016) and Macrophomina phaseolina (Dara et al., 2018) and reduce the disease severity. To further evaluate their efficacy against B. cinerea, these two fungi were also included in this study alternating with two chemical fungicides.
Treatments were applied with a CO2-pressurized backpack sprayer using 66.5 gpa spray volume. Five days before the first spray application and 3 days after each application, all ripe fruit were harvested from each plot and incubated at the room temperature in vented plastic containers. The level of gray mold on fruit from each plot was rated using a 0 to 4 scale (where 0=no disease, 1=1-25% fruit with fungal infection, 2=26-50% infection, 3=51-75%, and 4=76-100%) 3 and 5 days after each harvest (DAH). Due to the rains, fruit could not be harvested after the 3rd spray application for disease rating, but was harvested and discarded after the rains to avoid cross infection for the following week's harvest. Data were analyzed using analysis of variance using Statistix software and significant means were separated using Least Significant Difference separation test.
Results
Gray mold occurred at low to moderate levels during the study period. Along with B. cinerea, there were a few instances of minor fungal infections from Rhizopus spp. (Rhizopus fruit rot) and Mucor spp. (Mucor fruit rot). Pre-treatment disease ratings were statistically not significant (P = 0.6197 and 0.5741) 3 and 5 DAH. While the chemical standard treatment with the rotation of Captan, Merivon, Switch, and Pristine (treatment 2) appeared to result in the lowest disease rating throughout the observation period, treatments 3 and 5 after the 1st spray application, treatments 5 and 11 along with 3, 4 and 6 after the 2nd spray application, and treatments 3 and 5 along with 11 after the 4th spray application also had similar disease control at 3 DAH. When disease at 5 DAH was compared, the lowest rating was seen in treatment 2 after the 1st and 2nd spray applications, and treatments 2, 3, and 11 after the 4th application. Several other treatments also provided statistically similar control during these days.
When the average disease rating for the three post-treatment observation events was considered, treatment 2, 3, 5, and 11 had the lowest disease at both 3 and 5 DAH. Treatments 4 and 12 at 3 DAH also had a statistically similar level of disease control to treatment 2.
In general, most of the treatments provided moderate to high control compared to the disease in untreated control when the post-treatment averages were considered. Only treatment 7 and 13 had lower control at 3 DAH.
Discussion
This study compared a variety of registered and developmental products along with two entomopathogenic fungi in managing B. cinerea. Considering the fungicide resistance problem in B. cinerea in multiple crops, having multiple non-chemical control options is very important to achieve desirable control with integrated disease management strategies. Since the active ingredients in the botanical and bacterial fungicides used in this study are not public, discuss will be limited on their modes of action and efficacy at this point. Similarly, the active ingredient of WXF-17001 is also not known, however, an earlier study by Calvo-Garrido et al. (2014) demonstrated that a fatty acid-based natural product reduced B. cinerea conidial germination by 54% and disease severity in grapes by 96% compared to untreated control. The product used by Calvo-Garrido et al. (2014) is thought to be fungistatic and reduce the postharvest respiratory activity and ethylene production in fruits.
While chemical fungicides have a specific mode of action, biological and other products act in multiple manners either directly antagonizing the plant pathogen or by triggering the plant defenses. For example, amending the potting medium with biochar resulted in induced systemic resistance in tomato and reduced B. cinerea severity by 50% (Mehari et al., 2015). Luna et al. (2016) also showed that application of β-aminobutyric acid and jasmonic acid promoted seed germination and long-term resistance to B. cinerea in tomato. Burkholderia phytofirmans, beneficial endophytic bacterium, offered protection against B. cinerea in grapes by mobilizing carbon resources (callose deposition), triggering plant immune system (hydrogen peroxide production and priming of defense genese), and through antifungal activity (Miotto-Vilanova et al. 2016). Similarly, entomopathogenic fungi such as B. bassiana are also known to induce systemic resistance against plant pathogens (Griffin et al. 2006). Compared to other options evaluated in the study, entomopathogenic fungi have an advantage of controlling both arthropod pests and diseases, while also having plant growth promoting effect (Dara et al. 2017).
Rotating fungicides with different mode of actions reduces the risk of resistance development and using some combinations will also maintain control efficacy. This study provided the efficacy of multiple control options and their combinations and rotations for B. cinerea. This is also the first study demonstrating the efficacy of entomopathogenic fungi against B. cinerea in strawberry.
Acknowledgements: Thanks to Sipcam Agro and Westbridge for funding the study, technical assistance of Hamza Khairi for data collection, and the field staff at the Shafter Research Station for the crop maintenance.
References
Breeze, E. 2019. 97 Shades of gray: genetic interactions of the gray mold, Botrytis cinerea, with wild and domesticated tomato. The Plant Cell 31: 280-281. https://doi.org/10.1105/tpc.19.00030
Calvo-Garrido, C., A.A.G. Elmer, F. J. Parry, I. Viñas, J. Usall, R. Torres, R.H. Agnew, and N. Teixidó. 2014. Mode of action of a fatty acid-based natural product to control Botrytis cinerea in grapes. J. Appl. Microbiol. 116: 967-979. https://doi.org/10.1111/jam.12430
Dara, S. K., S. S. Dara, S.S.R. Dara, and T. Anderson. 2016. First report of three entomopathogenic fungi offering protection against the plant pathogen, Fusarium oxysporum f.sp. vasinfectum. UC ANR eJournal of Entomology and Biologicals https://ucanr.edu/blogs/blogcore/postdetail.cfm?postnum=22199
Dara, S. K., S.S.R. Dara, and S. S. Dara. 2017. Impact of entomopathogenic fungi on the growth, development, and health of cabbage growing under water stress. Amer. J. Plant Sci. 8: 1224-1233. https://doi.org/10.4236/ajps.2017.86081
Dara, S.S.R., S. S. Dara, and S. K. Dara. 2018. Preliminary report on the potential of Beauveria bassiana and Metarhizium anisopliae s.l. in antagonizing the charcoal rot causing fungus Macrophomina phaseolina in strawberry. UC ANR eJournal of Entomology and Biologicals https://ucanr.edu/blogs/blogcore/postdetail.cfm?postnum=28274
Griffin, M. R., B. H. Ownley, W. E. Klingeman, and R. M. Pereira. 2006. Evidence of induced systemic resistance with Beauveria bassiana against Xanthomonas in cotton. Phytopathol. 96.
Koike, S. T., G. T. Browne, T. R. Gordon, and M. P. Bolda. 2018. UC IPM pest management guidelines: strawberry (diseases). UC ANR Publication 3468. https://www2.ipm.ucanr.edu/agriculture/strawberry/Botrytis-Fruit-Rot/
Liu, S., Z. Che, and G. Chen. 2016. Multiple-fungicide resistance to carbendazim, diethofencardb, procymidone, and pyrimethanil in field isolates of Botrytis cinerea from tomato in Henan Province, China. Crop Protection 84: 56-61.
Luna, E., E. Beardon, S. Ravnskov, J. Scholes, and J. Ton. 2016. Optimizing chemically induced resistance in tomato against Botrytis cinerea. Plant Dis. 100: 704-710. https://doi.org/10.1094/PDIS-03-15-0347-RE
Mehari, Z. H., Y. Elad, D. Rav-David, E. R. Graber, and Y. M. Harel. 2015. Induced systemic resistance in tomato (Solanum lycopersicum) against Botrytis cinerea by biochar amendment involves jasmonic acid signaling. Plant and Soil 395: 31-44.
Miotto-Vilanova, L., C. Jacquard, B. Courteaux, L. Wortham, J. Michel, C. Clément, E. A. Barka, and L. Sanchez. 2016. Burkholderia phytofirmans PsJN confers grapevine resistance against Botrytis cinerea via a direct antimicrobial effect combined with a better resource mobilization. Front. Plant Sci. 7: 1236. https://doi.org/10.3389/fpls.2016.01236
Panebianco, A., I. Castello, G. Cirvilleri, G. Perrone, F. Epifani, M. Ferrarra, G. Polizzi, D. R. Walters, and A. Vitale. 2015. Detection of Botrytis cinerea field isolates with multiple fungicide resistance from table grape in Sicily. Crop Protection 77: 65-73.
Saito, S., T. J. Michailides, and C. L. Xiao. 2016. Fungicide resistance profiling in Botrytis cinerea populations from blueberry in California and Washington and their impact on control of gray mold. Plant Dis. 100: 2087-2093. https://doi.org/10.1094/PDIS-02-16-0229-RE
Saito, S., T. J. Michailides, and C. L. Xiao. 2019. Fungicide-resistant phenotypes in Botrytis cinerea populations and their impact on control of gray mold on stored table grapes in California. European J. Plant Pathol. 154: 203-213.
Stockwell, V. O., B. T> Shaffer, L. A. Jones, and J. W. Pscheidt. 2018. Fungicide resistance profiles of Botrytis cinerea isolated from berry crops in Oregon. Abstract for International Congress of Plant Pathology: Plant Health in A Global Economy; 2018 July 29-Aug 3; Boston, MA.
Weber, R.W.S. and M. Hahn. 2019. Grey mould disease of strawberry in northern Germany: causal agents, fungicide resistance and management strategies. Appl. Microbiol. Biotechnol. 103: 1589-1597.
- Author: Surendra K. Dara
There has been a growing interest in the recent years in exploring the potential of biostimulants in crop production. Biostimulants are mineral, botanical, or microbial materials that stimulate natural processes in plants, help them tolerate biotic and abiotic stressors, and improve crop growth and health. Several recent studies demonstrated the potential of the biostimulant or soil amendments in improving crop yields and health. For example, in a 2017 field study, silicon, microbial, botanical and nutrient materials improved processing tomato yields by 27 to 32% compared to the standard fertility program (Dara and Lewis, 2018). In a 2017-2018 strawberry field study, some biostimulant and soil amendment products resulted in a 13-16% increase in marketable fruit yield compared to the grower standard (Dara and Peck, 2018). He et al. (2019) evaluated three species of Bacillus and Pseudomonas putida alone and in different combinations in tomatoes grown in laboratory and greenhouse. The combination of Bacillus amyloliquefaciens, B. pumilus, and P. putida increased the plant biomass and the root/shoot ratio. Significant increase in fruit yield, between 18 and 39%, was also achieved from individual or co-inoculations of these bacteria. A field study was conducted in processing tomato to evaluate the impact of nutrient products containing beneficial microbes and botanical extracts on tomato yields and fruit quality.
Methodology
The study was conducted from late spring to fall of 2018 to evaluate three treatment programs compared to the grower standard. Tomato cultivar Quali T27 was seeded on 25 April and transplanted on 19 June using a mechanical transplanter. Due to high temperatures at the time of planting, some transplants died and they were re-planted on 28 June. Herbicide Matrix was applied on 5 July and Poast was applied on 13 July followed by hand weeding on 27 July. Crop was irrigated, fertigated, and treatements were applied through a drip system. Overhead sprinkler irrigation was additionally used immediately after transplanting. The following treatments were included in the study:
1. Grower standard: 10-34-0 Ammonium Polyphosphate Solution was applied at 10 gal/ac at the time of transplanting followed by the application of UAN-32 Urea Ammonium Nitrate Solution 32-0-0 at the rate of 15 units of N at 3, 6, and 13 weeks after planting and 25 units of N at 7 weeks after planting.
2. Grower standard + BiOWiSH Crop 16-40-0: BiOWiSH Crop 16-40-0 contains 16% nitrogen and 40% phosphate along with B. amyloliquefaciens, B. licheniformis, B. pumilus, and B. subtilis at 1X108 cfu/gram. Crop 16-40-0 was applied at 1 lb/ac at the time of planting followed by the application 0.5 lb/ac at 3, 6, and 9 weeks after planting.
3. Grower standard 85% + BiOWiSH Crop 16-40-0: Crop 16-40-0 was applied at the same rate and frequency as in treatment 2, but the grower standard was reduced to 85%.
4. RootRx: RootRx contains 5% soluble potash and proprietary botanical extracts and is supposed to stimulate a broad range of antioxidant compounds in the plant. It was applied at 0.25 gal/ac at the time of planting followed by the application of 0.5 gal/ac at 3, about 7, and 13 weeks after planting.
Each treatment contained 30' long bed with a single row of tomato plants and replicated five times in a randomized complete block design. Along with the fruit yield, the sugar content of the fruit and leaves [using a refractometer from three fruits (two measurements from each) and four leaves per plot], chlorophyll content (using a digital chlorophyll meter from four leaves per plot), and frost damage levels (using a visual rating on a 0 to 5 scale where 0 = no frost damage and 5 = extreme frost damage with a complete plant death) were also monitored. Due to an unknown reason, some plants in the fifth replication were stunted halfway through the study. Data from the fifth replication were excluded from the analysis. Data were subjected to the analysis of variance using Statistix software and significant means were separated using the Tukey's HSD test.
Results
Fruit yield: Marketable and unmarketable fruit yield was monitored from 27 August to 13 November. Seasonal total for marketable fruit was significantly (P = 0.04) different among the treatments where RootRx resulted in a 26.5% increase over the grower standard while Crop 16-4-0 with the full rate of the grower standard had an 8%, and with 85% of the grower standard had a 13.2% increase. It appeared that a similar improved yield response was also seen when Crop 16-40-0 was used at a reduced rate of the grower standard in other studies conducted by the manufacturer.
Sugar content: Sugar content of the fruit and leaves was measured once after the last harvest and there were no significant (P > 0.05) difference among the treatments.
Chlorophyll content: Chlorophyll content was measured once after the last harvest and there was no significant (P > 0.05) difference among the treatments.
Frost damage: Study was concluded after frosty conditions in November 2018 damaged the crop. Although there were no statistically significant (P > 0.05) differences, plants treated with RootRx had the lowest rating of 2.
Acknowledgements: Thanks to Jenita Thinakaran and the field staff at the Shafter Research Station for their technical assistance, Plantel Nurseries for providing transplants, and BiOWiSH Technologies and Redox Chemicals for their financial support.
References
Dara, S. K. and D. Peck. 2018. Microbial and bioactive soil amendments for improving strawberry crop growth, health, and fruit yields: a 2017-2018 study. UCANR eJournal of Entomology and Biologicals (https://ucanr.edu/blogs/blogcore/postdetail.cfm?postnum=27891)
Dara, S. K. and E. Lewis. 2018. Impact of nutrient and biostimulant materials on tomato crop health and yield. UCANR eJournal of Entomology and Biologicals (https://ucanr.edu/blogs/blogcore/postdetail.cfm?postnum=26054)
He. Y., H. A. Pantigoso, Z. Wu, and J. M. Vivanco. 2019. Co-inoculation of Bacillus sp. and Pseudomonas putida at different development stages acts as a biostimulant to promote growth, yield and nutrient uptake of tomato. J. Appl. Microbiol. https://doi.org/10.1111/jam.14273
- Author: Surendra K. Dara
- Author: Suchitra S. Dara
- Author: Alor Sahoo
- Author: Stefan Jaronski, USDA-ARS
The western Grapeleaf skeletonizer (WGLS), Harrisina metallica Stretch (Lepidoptera: Zygaenidae), previously known to cause severe defoliation to vineyards and backyard grapevines appears to be re-emerging in California. Since its first detection in San Diego in 1941, WGLS spread through commercial vineyards and backyard grapes becoming a serious problem. Although two biological control agents from Arizona and Mexico were introduced in California for WGLS control, a naturally occurring granulovirus (Harrisina brillians granulovirus) nearly eradicated WGLS populations and kept them under control. WGLS has not been a problem especially in conventional vineyards. However, based on some unpublished observations, WGLS populations are emerging in organic vineyards and backyard grapevines.
WGLS lives up to its name by skeletonizing and defoliating grape leaves. Organic vineyards are especially at risk and uncontrolled populations can destroy vineyards resulting in significant losses. Metallic bluish or greenish black moths lay barrel shaped yellowish eggs on the lower side of the leaves. There are five larval instars. Early instars are cream colored and develop black and purple bands in later stages. Pupation occurs in a whitish cocoon. Upon hatching, larvae start feeding side by side in a row on the lower side of leaf. Damage by younger larvae appears as whitish leaf area containing veins and the upper cuticle, which eventually turn brown. Older larvae skeletonize leaves leaving larger veins. Larvae may also feed on fruit leading to bunch rot. Severe damage can cause defoliation and sunburn of the exposed fruit.
Methodology
A study was conducted to evaluate the efficacy of six non-chemical control options that included formulations of spinosad, two subspecies of Bacillus thuringiensis, and a botanical insecticide/growth regulator along with two unformulated entomopathogenic fungal isolates native to California. Larvae were collected from an infested, untreated backyard grapevine and maintained in one gallon plastic tubs with screened lids on infested leaves. Fresh, untreated grape leaves from uninfested vines were provided daily for 3 days before starting the assay. For each treatment, five 4-5 instar larvae were placed on a grape leaf disc (rinsed in water and dried) in a Petri plate (100 mm dia) with a moist filter paper. Larvae were treated by spraying 1 ml of the treatment solution (containing Dyne-Amic as a surfactant at 0.125% vol/vol). Application rates for commercial formulations were determined based on label recommendations for 100 gallons of spray volume. Entomopathogenic fungal concentrations were also determined based on the label rates for similar commercial products. Treatments were replicated four times and the assay was conducted twice. Larval mortality was observed daily and dead larvae were removed and incubated separately. Fresh leaf discs were provided as needed to the remaining larvae. Actual and corrected (for control mortality) total mortality were calculated.Data were arcsine-transformed for statistical analysis and significant means were separated using Tukey's HSD test.
Results
Both cumulative daily mortality and total mortality significantly (P < 0.0001) differed among treatments. Entrust and M. anisopliae resulted in the highest mortality followed by B. bassiana, Neemix, and Agree. In general, feeding reduced or ceased in all larvae following treatment and could have contributed to a lower mortality in B. thuringiensis treatments. Entomopathogenic fungi emerged from all the cadavers from respective treatments. Microbial and botanical options provided good control of WGLS. These non-chemical alternatives can be effectively used in both organic and conventional vineyards. California isolates of B. bassiana and M. anisopliae demonstrated good control efficacy and the potential to be developed as microbial pesticides.
Acknowledgements: Thanks to the technical assistance of Alor Sahoo in carrying out these assays, and Certis and Corteva for providing the pesticide formulations.
References
Federici, B. A. and V. M. Stern. 1990. Replication and occlusion of a granulosis virus in larval and adult midgut epithelium of the western grapeleaf skeletonizer, Harrisina brillians. J. Invertebr. Pathol. 56: 401-414.
- Author: Sumanth S. R. Dara
- Author: Suchitra S. Dara
- Author: Surendra K. Dara
Charcoal rot, caused by Macrophomina phaseolina, is one of the important fungal diseases of strawberry in California. Macrophomina phaseolina is a soilborne fungus and has a wide host range, including alfalfa, cabbage, corn, pepper, and potato, some of which are cultivated in the strawberry production areas in California. The fungus infects the vascular system of the plant roots, obstructing the nutrient and water supply and ultimately resulting in stunted growth, wilting, and death of the plant. The fungus survives in the soil and infected plant debris as microsclerotia (resting structures made of hyphal bodies) and can persist for up to three years. Microslerotia germinate and penetrate the root system to initiate infection. Plants are more vulnerable to fungal infection when they are experiencing environmental (extreme weather or drought conditions) and physiological (heavy fruit bearing) stress.
Soil fumigation is the primary management option for addressing charcoal rot in strawberry. Crop rotation with broccoli can also reduce the risk of charcoal rot due to glucosinolates and isothiocyanates in broccoli crop residue that have fungicidal properties. Beneficial microorganisms such as Bacillus spp. and Trichoderma spp. are also considered, especially in organic strawberries, to antagonize M. phaseolina and other soilborne pathogens and provide some protection. The role of beneficial microbes in disease management or improving crop growth and health is gaining popularity in the recent years with the commercial availability of biofungicide, biostimulant, and soil amendment products. In a couple of recent strawberry field studies in Santa Maria, some of the beneficial microbial products improved fruit yield or crop health. These treatments can be administered by inoculating the transplants prior to planting, immediately after planting or periodically applying to the plants and or the soil. Adding beneficial microbes can help improve the soil microbiome especially after chemical or bio-fumigation and anaerobic soil disinfestation.
Similar to the benefits of traditionally used bacteria (e.g., Bacillus spp. and Pseudomonas spp.) and fungi (e.g., Glomus spp. and Trichoderma spp.), studies with entomopathogenic fungi such as Beauveria bassiana, Isaria fumosorosea, and Metarhizium spp. also demonstrated their role in improving water and nutrient absorption or antagonizing plant pathogens. The advantage of entomopathogenic fungi is that they are already used for arthropod pest management in multiple crops, including strawberry; now, there are the additional benefits of promoting crop growth and antagonizing plant pathogens. In light of some promising recent studies exploring these roles, a study was conducted using potted strawberry plants to evaluate the efficacy of two California isolates of Beauveria bassiana and Metarhizium anisopliae s.l. and their application strategies against M. phaseolina.
Methodology
About 6 week old strawberry plants (cultivar Albion) from a strawberry field at the Shafter Research Station were transplanted into 1.6-gallon pots with Miracle-Gro All Purpose Garden Soil (0.09-0.05-0.07 N-P-K) and maintained in an outdoor environment. They were regularly watered, and their health was monitored for about 5 months prior to the commencement of the study. Conidial suspensions of the California isolates of B. bassiana and M. anisopliae s.l. were applied one week before, after, or at the time of applying microsclerotia of M. phaseolina to the potting mix. The following treatments were evaluated in the study:
- Untreated control
- Soil inoculated with M. phaseolina
- Soil inoculated with B. bassiana 1 week prior to M. phaseolina inoculation
- Soil inoculated with M. anisopliae s.l. 1 week prior to M. phaseolina inoculation
- Soil inoculated with B. bassiana at the time of M. phaseolina inoculation
- Soil inoculated with M. anisopliae s.l. at the time of M. phaseolina inoculation
- Soil inoculated with B. bassiana 1 week after to M. phaseolina inoculation
- Soil inoculated with M. anisopliae s.l. 1 week after to M. phaseolina inoculation
Entomopathogenic fungi were applied as 1X1010 viable conidia in 100 ml of 0.01% Dyne-Amic (surfactant) solution distributed around the plant base. To apply M. phaseolina, 5 grams of infested cornmeal-sand inoculum containing 2,500 CFU/gram was added to four 5 cm deep holes around the base of the plant. Each treatment had six pots each planted with a single strawberry plant representing a replication. Treatments were randomly arranged within each replication. The study was repeated once a few days after the initiation of the first experiment.
Plant health was monitored starting from the first week after the M. phaseolina inoculation and continued for seven weeks. Plant health was rated on a scale of 0 to 5 where 0=dead and 5=very healthy and the rest of the ratings in between depending on the extent of wilting. Data from both experiments were combined and analyzed by ANOVA using Statistix software and significant means were separated using LSD test. The influence of entomopathogenic fungal treatments applied at different times as well as the combined effect of different applications within each fungus were compared for seven weeks. Ratings for some plants that were scorched from hot summer temperatures and died abruptly were removed from the analyses.
Results
Untreated control plants maintained good health throughout the observation period varying between the rating of 4.3 and 4.9. In general, plant health declined considerably from the 5th week after M. phaseolina inoculation. Plant health appeared to be slightly better in plants treated with entomopathogenic fungi, but there was no statistically significant difference in any except one instance. Plants treated with M. anisopliae one week prior to the application of M. phaseolina had a rating of 3.0 compared to 1.6 rating of plants inoculated with M. phaseolina alone.
When data from different treatments for each entomopathogenic fungus were compared, both B. bassiana and M. anisopliae s.l. appeared to reduce the wilting, but the plant health rating was not significantly different from the M. phaseolina treatment alone.
This is the first report of the impact of entomopathogenic fungi on M. phaseolina with some promise. Additional studies under more uniform environmental conditions and with more treatment options would shed more light on this approach of using entomopathogenic fungi against M. phaseolina. The current study evaluated single application of the entomopathogenic fungi and we plan to conduct additional studies with multiple applications.
Acknowledgements: We thank Dr. Kelly Ivors (previously at Cal Poly San Luis Obispo) for the pathogen inoculum and Dr. Stefan Jaronski, USDA-ARS, Sidney, MT for multiplying the entomopathogenic fungal inocula.
References
Dara, S. K. and D. Peck. 2017. Evaluating beneficial microbe-based products for their impact on strawberry plant growth, health, and fruit yield. UC ANR eJournal Strawberries and Vegetables. https://ucanr.edu/blogs/blogcore/postdetail.cfm?postnum=25122
Dara, S. K. and D. Peck. 2018. Evaluation of additive, soil amendment, and biostimulant products in Santa Maria strawberry. CAPCA Adviser, 21(5): 44-50.
Dara, S. K., S.S.R. Dara, and S. S. Dara. 2017. Impact of entomopathogenic fungi on the growth, development, and health of cabbage growing under water stress. Amer. J. Plant Sci. 8: 1224-1233. http://file.scirp.org/pdf/AJPS_2017051714172937.pdf
Dara, S. K., S. S. Dara, S.S.R. Dara, and T. Anderson. 2016. First report of three entomopathogenic fungi offering protection against the plant pathogen, Fusarium oxysporum f.sp. vasinfectum. UC ANR eJournal Strawberries and Vegetables. https://ucanr.edu/blogs/blogcore/postdetail.cfm?postnum=22199
Koike, S. T., G. T. Browne, and T. R. Gordon. 2013. UC IPM pest management guidelines: Strawberry diseases. UC ANR Publication 3468. http://ipm.ucanr.edu/PMG/r734101511.html
Partridge, D. 2003. Macrophomina phaseolina. PP728 Pathogen Profiles, Department of Plant Pathology, North Carolina State University. https://projects.ncsu.edu/cals/course/pp728/Macrophomina/macrophominia_phaseolinia.HTM
Vasebi, Y., N. Safaie, and A. Alizadeh. 2013. Biological control of soybean charcoal root rot disease using bacterial and fungal antagonists in vitro and greenhouse condition. J. Crop Prot. 2(2): 139-150.
- Author: Surendra K. Dara
Integrated pest management, commonly referred to as IPM, is a concept of managing pests that has been in use for several decades. The definition and interpretation of IPM vary depending on the source, such as a university, institute, or a researcher, and its application varies even more widely depending on the practitioner. Here are a few examples of its definitions and interpretations:
“IPM is an ecosystem-based strategy that focuses on long-term prevention of pests or their damage through a combination of techniques such as biological control, habitat manipulation, modification of cultural practices, and use of resistant varieties. Pesticides are used only after monitoring indicates they are needed according to established guidelines, and treatments are made with the goal of removing only the target organism. Pest control materials are selected and applied in a manner that minimizes risks to human health, beneficial and nontarget organisms, and the environment.” UC IPM
“Integrated Pest Management, or IPM, is an approach to solving pest problems by applying our knowledge about pests to prevent them from damaging crops, harming animals, infesting buildings or otherwise interfering with our livelihood or enjoyment of life. IPM means responding to pest problems with the most effective, least-risk option.” IPM Institute of North America
“A well-defined Integrated Pest Management (IPM) is a program that should be based on prevention, monitoring, and control which offers the opportunity to eliminate or drastically reduce the use of pesticides, and to minimize the toxicity of and exposure to any products which are used. IPM does this by utilizing a variety of methods and techniques, including cultural, biological and structural strategies to control a multitude of pest problems.” Beyond Pesticides
“IPM is rotating chemicals from different mode of action groups.” A grower
These definitions and interpretations represent a variety of objectives and strategies for managing pests. IPM is not a principle that can/should be strictly and equally applied to every situation, but a philosophy that can guide the practitioner to use it as appropriate for the situation. For example, varieties that are resistant to arthropod pests and diseases are available for some crops, but not for others. Mating disruption with pheromones is widely practiced for certain lepidopteran and coleopteran pests, but not for several hemipteran pests. Biological control is more readily employed for greenhouse pests, but not to the same extent under field conditions. While chemical pesticides should be used as the last resort, in principle, sometimes they are the first line of defense to prevent damage to the transplants by certain pests or area-wide spread of certain endemic or invasive pests and diseases.
Crop production is an art, science, and business, and by adding environmental and social factors, IPM – an approach used in agriculture – can also be influenced by a number of factors. Each grower has their own strategy for producing crops, minimizing losses, and making a profit in a manner that is acceptable to the society, safe for the consumers, and less disruptive to the environment. In other words, “IPM is an approach to manage pests in an economically viable, socially acceptable, and environmentally safe manner”. Keeping this simple, but loaded, definition in mind and considering recent advances in crop production and protection, communication technology, and globalization of agriculture and commerce, here is the new paradigm of IPM with its management, business, and sustainability aspects.
I. Management Aspect
There are four major components in the IPM model that address the various pest management options, the knowledge and resources the grower has in order to address the pest issue, planning and organization of information to take appropriate actions, and maintaining good communication to acquire and disseminate knowledge about pests and their management.
1. Pest Management:
The concept of pest control has changed to pest management over the years knowing that a balanced approach to managing pest populations to levels that do not cause economic losses is better than eliminating for environmental and economic reasons. Although the term control is frequently used in literature and conversations, it generally refers to management. A thorough knowledge of general IPM principles and various management options for all possible pest problems is important as some are preventive and others are curative. It is also essential to understand inherent and potential interactions among these management options to achieve maximum control. The following are common control options that can be employed at different stages of crop production to prevent, reduce, or treat pest infestations. Each of them may provide only a certain level of control, but their additive effect can be significant in preventing yield losses.
a. Host plant resistance: It involves the use of pest resistant and tolerant cultivars developed through traditional breeding or genetic engineering. These cultivars possess physical, morphological, or biochemical characters that reduce the plant's attractiveness or suitability for the pest to feed, develop, or reproduce successfully. These cultivars resist or tolerate pest damage and thus reduce the yield losses.
b. Cultural control: Changing agronomic practices to avoid or reduce pest infestations and damage refers to cultural control. Adjusting planting dates can help escape pest occurrence or avoid most vulnerable stages. Modifying irrigation practices, fertilizer program, plant or row spacing, and other agronomic practices can create conditions that are less suitable for the pest. Destroying crop residue and thorough cultivation will eliminate breeding sites and control soil-inhabiting stages of the pest. Crop rotation with non-host or tolerant crops will break the pest cycles and reduce their buildup year after year. Choosing clean seed and plant material will avoid the chances of introducing pests right from the beginning of the crop production. Sanitation practices to remove infected/infested plant material, regular cleaning field equipment, avoiding accidental contamination of healthy fields through human activity are also important to prevent the pest spread. Intercropping of non-host plants or those that deter pests or using trap crops to divert pests away from the main crop are some of the other cultural control strategies.
c. Biological control: Natural enemies such as spiders, predators, and parasitic wasps can be very effective in causing significant reductions in pest populations in certain circumstances. Periodical releases of commercially available natural enemies or conserving natural enemy populations by providing refuges or avoiding practices that harm them are some of the common practices to control endemic pests. To address invasive pest issues, classical biological control approach is typically employed where natural enemies from the native region of the invasive pest are imported, multiplied, and released in the new habitat of the pest. The release of irradiated, sterile insects is another biological control technique that is successfully used against a number of pests.
d. Behavioral control: Behavior of the pest can be exploited for its control through baits, traps, and mating disruption techniques. Baits containing poisonous material will attract and kill the pests when distributed in the field or placed in traps. Pests are attracted to certain colors, lights, odors of attractants or pheromones. Devices that use one or more of these can be used to attract, trap or kill pests. Pheromone lures confuse adult insects and disrupt their mating potential, and thus reduce their offspring.
e. Physical or mechanical control: This approach refers to the use of a variety of physical or mechanical techniques for pest exclusion, trapping (in some cases similar to the behavioral control), removal, or destruction. Pest exclusion with netting, handpicking or vacuuming to remove pests, mechanical tools for weed control, traps for rodent pests, modifying environmental conditions such as heat or humidity in greenhouses, steam sterilization or solarization, visual or physical bird deterrents such as reflective material or sonic devices are some examples for physical or mechanical control.
f. Microbial control: Using entomopathogenic bacteria, fungi, microsporidia, nematodes, and viruses, and fermentation byproducts of microbes against arthropod pests, fungi against plant parasitic nematodes, and bacterial and fungal antagonizers of plant pathogens generally come under microbial control.
g. Chemical control: Chemical control typically refers to the use of synthetic chemical pesticides, but to be technically accurate, it should include synthetic chemicals as well as chemicals of microbial or botanical origin. Although botanical extracts such as azadirachtin and pyrethrins, and microbe-derived toxic metabolites such as avermectin and spinosad are regarded as biologicals, they are still chemical molecules, similar to synthetic chemicals, and possess many of the human and environmental safety risks as chemical pesticides. Chemical pesticides are categorized into different groups based on their mode of action and rotating chemicals from different groups is recommended to reduce the risk of resistance development. Government regulations restrict the time and amount of certain chemical pesticides and help mitigate the associated risks.
The new RNAi (ribonucleic acid interference) technology where double-stranded RNA is applied to silence specific genes in the target insect is considered as a biopesticide application. Certain biostimulants based on minerals, microbes, plant extracts, seaweed or algae impart induced systemic resistance to pests and diseases, but are applied as amendments without any claims for pest or disease control. These new products or technologies can fall into one or more abovementioned categories.
As required by the crop and pest situation, one or more of these control options can be used throughout the production period for effective pest management. When used effectively, non-chemical control options delay, reduce, or eliminate the use of chemical pesticides.
2. Knowledge and Resources:
The knowledge of various control options, pest biology and damage potential, and suitability of available resources enables the grower to make a decision appropriate for their situation.
a. Pest: Identification of the pest, understanding its biology and seasonal population trends, damaging life stages and their habitats, nature of damage and its economic significance, vulnerability of each life for one or more control options, host preference and alternate hosts, and all the related information is critical for identifying an effective control strategy.
b. Available control options: Since not all control options can be used against every pest, the grower has to choose the ones that are ideal for the situation. For example, systemic insecticides are more effective against pests that mine or bore into the plant tissue. Pests that follow a particular seasonal pattern can be controlled by adjusting planting dates. Commercially available natural enemies can be released against some, while mating disruption works well against others. Entomopathogenic nematodes can be used against certain soil pests, bacteria and viruses against pests with chewing mouthparts such as lepidoptera and coleopteran, and fungi against sucking pests.
c. Tools and technology: A particular pest can be controlled by certain options, but they may not all be available in a particular place, for a particular crop, or within the available financial means. For example, the release of natural enemies may be possible in high-value speciality crops, but not in large acreage field crops. A particular pesticide might be registered against a pest on some crops, but not on all. Use of netting or tractor-mounted vacuums can be effective, but very expensive limiting their availability to those who can afford.
This is a critical component where diagnostic and preventive or curative decisions are made based on available and affordable control options.
3. Planning and Organization:
This component deals with the management aspect of the of the new IPM model for data collection, organization, and actual actions against pest infestations.
a. Pest monitoring: Regularly monitoring the fields for pest infestation and spread is a basic step in crop protection. Early detection in many cases can help address the pest situation by low-cost spot treatment or removal of pests or infected/infested plant material. When pest infestations continue to grow, regular monitoring is necessary to assess the damage and determine the time to initiate farm-wide control. Monitoring is also important to avoid calendar-based pesticide applications especially at lower pest populations that do not warrant treatments.
b. Managing information: A good recordkeeping about pests, their damage, effective treatments, seasonal fluctuations, interactions with environmental factors, irrigation practices, plant nutrition, and all related information from year to year will build the institutional knowledge and prepares the grower to take preventive or curative actions.
c. Corrective actions: Taking timely action is probably the most important aspect of IPM. Even with all the knowledge about the pest and availability of resources for its effective management, losses can be prevented only when corrective actions are taken at the right time. Good farm management will allow the grower to take timely actions. These actions are not only necessary to prevent damage on a particular farm, but also to prevent the spread to neighboring farms. When pest management is neglected, it leads to area-wide problems with larger regulatory, social, and economic implications.
4. Communication:
Good communication to transfer the individual or collective knowledge for the benefit of everyone is the last component of the new IPM model. Modern and traditional communication tools can be used for outreach as university and private researchers develop information about endemic and invasive pests, emerging threats, and new control strategies.
a. Staying informed: Growers and pest control professionals should stay informed about existing and emerging pests and their management options. Science-based information can be obtained by attending extension meetings, webinars, or workshops, reading newsletter, trade, extension, or scientific journal articles, and keeping in touch with researchers and other professionals through various communication channels. Well-informed growers can be well prepared to address pest issues.
b. Communication within the group: Educating farm crew through periodical training or communication will help with all aspects of pest management, proper pesticide handling, ensuring worker safety, and preventing environmental contamination. Knowledgeable field crew will be beneficial for effective implementation of pest management strategies.
c. Communication among growers: Although certain crop production and protection strategies are considered proprietary information, pests do not have boundaries and can spread to multiple fields when they are not effectively managed throughout the region. Sharing knowledge and resources with each other will improve pest control efficacy and benefit the entire grower community.
In addition to these four components with an IPM model, factors that influence profitable, safe, and affordable food production at a larger scale and their implications for global food security should also be included. There are two layers surrounding these four components addressing the business and sustainable aspects of food production.
II. Business Aspect:
Consumers want nutritious, healthy, and tasty produce that is free of pest damage at affordable prices. Growers try to meet this demand by producing food that meets all the consumer needs, while maintaining environmental and human safety and still being able to make a profit. Sellers evaluate the market demand and strategize their sales to satisfy consumers while making their own profit to stay in the business. In an ideal system, consumer, producer, and seller would maintain a harmonious balance of food production and sale. In such a system, food is safe and affordable to everyone, there will be food security all over the world, and both growers and sellers make a good profit with no or minimal risk to the environment in the process of food production. However, this balance is frequently disrupted due to i) consumers' misunderstanding of various food production systems, their demand for perfectly shaped fruits and vegetables at affordable prices or their willingness to pay a premium price for food items that are perceived to be safe, ii) growers trying to find economical ways of producing high quality food while facing with continuous pest problems and other challenges, and iii) sellers trying to market organic food at a higher price as a safer alternative to conventionally produced food. If growers implement good IPM strategies to produce safe food and consumers are aware of this practice and gain confidence in food produced in an IPM system, then sellers would be able to market what informed-consumers demand.
III. Sustainability Aspect:
As mentioned earlier, IPM is an approach to ensure economic viability at both consumer and producer level (seller is always expected to make a profit), environmental safety through a balanced use of all available pest control options, and social acceptability as food is safe and affordable.
While organic food production is generally perceived as safe and sustainable, the following examples can explain why it is not necessarily true. Organic food production is not pesticide-free and some of the pesticides used in an organic system are as harmful to humans and non-target organisms as some chemical pesticides. Certain organically accepted pesticides have toxins or natural chemical molecules that are very similar to those in synthetic pesticides. In fact, some synthetic pesticides are manufactured imitating the pesticidal molecules of natural origin. Mechanical pest control practices such as vacuuming or tilling utilize fossil fuels and indirectly have a negative impact on the environment. For example, diesel-powered tractors are operated for vacuuming western tarnished bug in strawberry 2-3 times or more each week while a pesticide application typically requires the use of tractor once every 7-14 days. To control certain pests, multiple applications of organic pesticides might be necessary with associated costs and risks, while similar pest populations could be controlled by fewer chemical pesticide applications. It is very difficult to manage certain plant diseases and arthropod pests through non-chemical means and inadequate control not only leads to crop losses, but can result in their spread to larger areas making their control even more difficult. Many growers prefer a good IPM-based production to an organic production for the ease of operation and profitability. However, they continue to produce organic food to stay in business.
While middle and upper-class consumers may be willing to pay higher prices for organically produced food, many of the low-income groups in developed and underdeveloped countries cannot afford such food. Organic food production can lead to social inequality and a false sense of wellbeing for those can afford. Food security for the growing world population is necessary through optimizing input costs, minimizing wastage, grower adoption of safe and sustainable practices, and consumer confidence in food produced through such practices. IPM addresses all the economic, environmental, and social aspects and provides safe and affordable food to the consumers and profits to producers and sellers, while maintaining environmental health.