Progress report for SW22-936
Project Information
Sweet potato is economically and culturally important in Hawaii. Sweet potato was the highest revenue-generating vegetable crop in Hawaii until challenged by multiple pests, in particular the sweet potato weevil (Cylas formicarius elegantulus). While weevil feeding may cause vine damage, the more serious problem is to the tubers. Larvae tunnel resulting in spongy tuber that is dark in color. Additionally, larval feeding causes tubers to develop a bitter taste and a terpene odor. Losses to the weevil range from 30 to 97% across farms. Producers in Hawaii have turned to pesticide-intensive management tactics spanning the time from planting to harvest. Growers sometimes rely upon weekly insecticide applications to ensure a marketable crop. Non-chemical based integrated pest management strategies are needed and entomopathogenic nematodes (EPN) are a promising candidate.
The weevils are susceptible to Heterorhabditis sp. and Steinernema sp. These EPN have met with some success in managing sweet potato weevils in other growing areas. We propose to use EPN-infected larvae, sometimes called living bombs, to control the sweet potato weevil. Living bombs, or EPN-infected larvar, entail placement of the EPN-infected insect cadavers into the field rather than aqueous application of Infective Juveniles (IJ) that have exited the cadaver and been collected.
One objective will be to demonstrate the efficacy of H. indica and S. feltiae in reducing weevil damage in sweet potato in Hawaii. Traditional EPN application methods utilize inundative release of billions of EPN/ha in an aqueous solution. Delivery of the EPN in cadavers will allow for lower numbers and a consequently less expensive tool for growers. Another objective will be to compare the efficacy of different delivery methods of H. indica and S. feltiae. All EPN applications (sprays or bombs) will be compared to the standard practices of cooperating sweet potato producers. Since the focus is to transfer pipeline technologies to growers, our final objective is to convey the information to growers and other practitioners. We will develop videos, extension publications, newsletter articles, and scientific publications to share information. Initially, we will serve as a source for the EPN via a fee-for-service while the nascent demand for EPN builds and before commercial operations enter the Hawaii market. The potential impact of the project is the adoption of environmentally safe and sound biological control for sweet potato weevil by the key sweet potato producers that will then model and influence adoption by fellow sweet potato growers. The co-PIs have statewide connections to share project outcomes through social media, e-mail lists, and newsletters. The project team will work closely with leading growers and extension agents to foster adoption. Our longterm goal is to promote sustainable sweet potato cultivation through economic and environmentally sound pest management.
We propose to use Entomopathogenic Nematode (EPN) infected cadavers, or living bombs, to control the sweet potato weevil. We have two research objectives and three educational objectives. Our research objective 1 will be to demonstrate the efficacy of Heterodera indica and Stienernema feltiae, different species of EPN, in reducing weevil damage in sweet potato. Research objective 2 will be to compare the efficacy of spray applications to living bomb delivery of H. indica and S. feltiae documenting that fewer EPN are needed for effective weevil management when delivered as living bombs. Our educational objectives are (1) to impart knowledge about EPN for IPM control of sweet potato weevil, (2) to illustrate the application of EPN living bombs, and (3) to demonstrate the utility of EPN living bombs as an additional IPM tool for control of sweet potato weevils.
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1. Efficacy |
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2. Application Comparison |
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Analysis |
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1. Impart knowledge field days |
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2. Illustrate living bombs workshops |
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3. Assess utility |
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Videos |
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Reporting |
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The boxes show the initiation and the completion of the different activities. Field days and workshops boxes represent the quarter in which the one-day events will be held. For newsletters, the boxes represent publication quarter.
Cooperators
- - Producer
- - Producer
- - Producer
- (Educator and Researcher)
Research
Two locally-isolated EPN, H. indica and S. feltiae, will be reared on waxworms (Galleria mellonella) or mealworms (Tenebrio molitor) in the laboratory. Mealworm larvae will be exposed to EPN in a filter paper-lined petri dish and cadavers transferred to White traps to collect emerging Infective Juveniles (IJ). IJ will be held at 15℃ until application but no longer than 30 days. These IJ will serve as source cultures and as the source for aqueous applications of IJ. For the EPN-infected cadaver applications, dead larvae will be applied directly to the field or the larvae will be desiccated for easier handling. Infected larvae will be desiccated in a saturated KCl solution for 2 weeks. Production of the desiccated cadavers will be timed to coincide with the desired application window.
Sweet potato is cultivated continuously in Hawaii, thus allowing demonstrations to be established throughout the year. Growers generally produce their own planting material from cuttings. Tests will be conducted on cooperator farms utilizing the standard practices of that farm which may vary slightly from field to field.
Demonstration of the efficacy of H. indica and S. feltiae (Objective 1): Demonstrations will be established in each producers’ field. The demonstrations will consist of a no-weevil treatment, standard producer practice (this varies among the cooperators), a postplant application of H. indica, and a postplant application of S. feltiae. Plots size and layout will vary and be tailored to each cooperators operation. EPN will be applied when roots begin to swell, often about 4 months after planting, and monthly until harvest. The EPN will be applied at 2 x 109 IJs/ha as an aqueous spray and as EPN-infected cadavers. Aqueous applications will be directed under the leaves and at the plant stems. EPN_infected cadavers will be placed on the ground near sweet potato stems at regular intervals to achieve the desired rate. At harvest, sweet potato yield will be recorded. Weevil damage to the swollen roots will be evaluated and a random 1 kg swollen root sample will be assayed for weevil population density and life stages. As general target, plots will be 2 beds wide by 5 m long. Treatments will be randomized with 4 replications on each farm. Data will be analyzed for variance and differences among treatments. A field day will be held to highlight difference and educate other growers of the potential for EPN as a management tool.
Comparison of application methods (Objective 2): Similar to Objective 1, demonstrations will be established in each producers’ field consisting of a no weevil treatment, the standard producer practice, a postplant aqueous application of H. indica, an EPN-infected cadaver application of H. indica, a postplant aqueous application of S. feltiae, and an EPN-infected cadaver application of S. feltiae. EPN will be applied when the sweet potato roots begin to swell. Application rates will all be equivalent to 2 x 109 IJs/ha. One-week-old EPN-infected cadavers will be used. At harvest, sweet potato yield will be recorded. Weevil damage to the swollen roots will be evaluated and a random 1 kg swollen root sample will be assayed for weevil population density. Data will be analyzed for variance and differences among treatments.
Outreach: Video will be taken of the spray application and bomb application to educate growers in the appropriate techniques to apply EPN for sweet potato management. Field days will be scheduled to highlight efficacy and differences among treatments and to educate other growers of EPN as a management tool.
Sweet potato weevil causes serious yield loss to growers wherever sweet potato is grown, including Hawaii. Current grower practices rely upon regular pesticide applications which have environmental, economic, and societal drawbacks. We have completed several field experiments and demonstrations to show how Entomopathogenic Nematodes (EPN) can be incorporated into the sweet potato cropping cycle to manage sweet potato weevils and reduce insecticide usage.
One field experiment focused on demonstrating the comparative effectiveness of Heterorhabditis indica and Steinernema feltiae, two EPNs, in aqueous and cadaver applications. EPN-infected cadavers or living bombs provide the EPN a more protected environment and result in applications of where the EPN are more effective. The EPN-infected cadavers tested were larvae of Galleria mellonella. This field experiment consisted of cadavers infected with H. indica, cadavers infected with S. feltiae, aqueous application of H. indica, aqueous application of S. feltiae; and an untreated water control. Plots were planted with 20-cm long slips of Ipomea batatas Okinawan and EPN treatments commenced once sweet potato roots began to swell, around 3 months after planting. The EPN treatments were applied monthly until harvest or 4 to 6 months after planting. The EPN-infected cadaver treatment rate was based on average EPN yield recorded for a cadaver in the laboratory such that EPN-infected cadaver and aqueous applications were at 2.0 x 109 IJs/ha. At harvest, sweet potato yield was recorded, swollen roots were graded, and a subsample of sweet potato was assayed for sweet potato weevil infection.
The sweet potato weevil pressure was low in the test field. Less than 10 males were captured in a pheromone trap during the entire sweet potato growth period. Consequently, few sweet potato roots were damaged by the weevil even in the untreated controls. Nevertheless, plots treated with S. feltia-infected cadavers and plots receiving aqueous sprays of H. indica had the highest yields which was greater than the untreated control (P<0.05). We attribute the increased yield to the effects that the EPNs had on other aspects of soil-surface and soil biological community.
A second field demonstration was conducted to optimize application rates for the EPN-infected cadavers for effective sweet potato weevil control. Plots were established similar to the ones in the previous demonstration. When sweet potato root swelling commenced, the EPN-infected cadavers were applied on the soil under the sweet potato canopy. Larvae of G. mellonella infected with H. indica were used in this test. Four treatments were evaluated consisting of 0 IJ/ha, 1 x 109 IJs/ha (0.5X), 2 x 109 IJs/ha (1X), or 4 x 109 IJs/ha (2X). Sweet potato harvest data similar to the previous demonstration was collected.
Similar to the previous field, sweet potato weevil pressure in the field was low with little loss even in the untreated plots. However, the 0.5X application rate or 1 x 109 IJs/ha resulted in the greatest sweet potato yield of all treatments (P<0.05). It may have been that the higher rates of cadaver application resulted in greater predation of the cadavers by geckos, birds, or ants in the field, thus reducing the actual amount to EPN application.
Another series of experiments have been undertake to facilitate the application of EPN-infected cadavers. The infected cadavers can be challenging to transport and apply in the field. A gentle hand is required so as not to break the cadavers and allow the EPN to be exposed prematurely. Desiccation of the cadavers, or removal of 15% of their moisture, resulting in EPN-infected cadavers that are leather like. These leather-like cadavers are easier to transport and less likely to rupture when applied in the field.
Laboratory experiments were conducted with larvae of G. mellonella infected with H. indica that were desiccated to 85% relative humidity. The desiccated larvae are leathery and not as prone to rupture during handling. IJ emergence did not differ between non-desiccated and desiccated larvae. The average IJ emergence of both desiccated and non-desiccated larvae was 107,564 and 116,049 IJs/cadave, respectively (P<0.05). No difference was observed in IJs during subsequent infection of G. mellonella larvae. Both the desiccated and non desiccated IJs resulted in 100% mortality of G. mellonella. Desiccation does not appear to adversely IJ. Future research should investigate holding desiccated cadavers for longer periods as a means to store cadavers for future use.
Steinernema feltiae was less desirable as a candidate for desiccation due to IJ emergence from the host insect cadaver during desiccation. Galleria mellonella infected with S. feltiae were easily ruptured during handling and application. Cadavers of G. mellonella deteriorated rapidly when infected with S. feltiae. When Tenebrio molitar was used as the host, IJ of S. feltiae would emerge during the desiccation process. This early emergence of IJ lessens the potential effectiveness of the EPN application. These two reasons-fragility of cadavers and early IJ emergence, made S. feltiae a less than ideal candidate for EPN-infected cadaver application.
Heterorhabditis indica is a good candidate for desiccation and storage when reared on G. mellonella. H. indica is not adversely affected by desiccation and the desiccated cadavers are easier to apply in the field.
A large plot field experiment was conducted to elucidate the effectiveness of desiccated EPN-infected cadavers. Cadavers were applied at a rate equivalent to2.0 x 109 IJs/ha commencing when sweet potato roots began to swell, about 4 months after planting. EPN were applied monthly until harvest. Other treatment applications included a Metarhizium-amended mulch and post-plant application of Metarhizium. The EPN-infected cadaver applications reduced sweet potato weevil damage compared to the untreated controls but not as much as the Metarhizium-amended mulch plots. Plants in the Metarhizium-amend mulch plots tended to be larger than the other plots regardless of postplant treatments. A noticeable yield gradient was evident in total yields from replication 1 to replication 4. It is likely that EPN application should have commenced sooner to offer earlier protection from the sweet potato weevils.
Research Outcomes
Our preliminary recommendations for the use of EPN in a sweet potato cropping system are multi-fold. Timing of EPN application is critical. We are learning that applying EPN when the sweet potato roots begin to swell is probably too late. EPNs need to be present early to prevent the sweet potato weevils from laying eggs in the plant stems. The sweet potato weevils are cryptic and it is not clear where they spend their time, so the EPN must be present almost at the time of planting. Another lession that we are learning is the EPN-cadaver (living bomb) application appears to be as effective the aqueous applications. This may occur since we are targetting the aqueous application to the undersides of the leaves and the EPN on the underside of the leaves are protected from UV light as are the the EPN in the cadaver. Finally we are learning that to effectively use EPN for sweet potato weevil control, the weevil population and subsequent pest pressure must not be too high. EPNs preform best at low to moderate pest pressure.
Education and Outreach
Participation Summary:
Thus far, the greatest educational and outreach result has been the recognition of EPN as a possible biological control agent against insect pests. This assessment is supported by the questions asked and interest expressed in EPN for insect management. Growers are more aware of the EPN alternative and seek more information around the use and availability of EPN for insect control.
Education and Outreach Outcomes
Our educational and outreach activites have highlighted producer interest in EPN. This interest can be facilitated and encouraged by providing addtional online resources for growers. This is motivation to keep EPN as biological control organisms in producers' minds. Growers seem to be more satisfied with in-person interactions than solely electronic interactions.
- Entomopathogenic nematodes
- Biological control options
Entomopathogenic nematodes