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Season-long comparison of trap lures for integrated management of the navel orangeworm (Lepidoptera: Pyralidae) in almond and pistachio
CABI Agriculture and Bioscience volume 5, Article number: 30 (2024)
Abstract
Monitoring navel orangeworm, Amyelois transitella (Lepidoptera: Pyralidae) using pheromone lures is now complicated by the use of mating disruption. Two commercially available lures that are minimally affected by mating disruption use either natural ovipositional substrates (Bait lures) or a combination of phenyl propionate (PPO), a volatile chemical that attracts both sexes and pheromone lures (Combo lures). We compared the season-long trap capture for these two lures in a sterile insect technique (SIT) demonstration project in Fresno County, California, 2020–2023. A total of 194,233 males (96.52%) were caught using Combo lures and 7006 (3.48%) caught using Bait lures, while 95,947 females (48.83%) were caught using Combo lures and 100,532 (51.17%) caught using Bait lures. Capture of A. transitella was 2.3-fold higher in pistachio (278,492) than in almond (119, 316), and within a commodity, there was a moderate correlation in female capture between the two lures; correlation was stronger during the period leading up to July 21 (Julian date 202). For Bait lures, 48.7% of the trap catch in almond occurred by July 21 and 87.1% of the trap catch occurred in pistachio by July 21. For Combo lures, 38.9% of the trap catch in almond occurred by July 21 while 54.6% of the catch occurred in pistachio. Bait lures became less effective after July 21, likely due to diminished attractiveness as new crop nuts split in August through October. Our data indicate that Combo lures are preferable when the goal is consistent season-long capture of A. transitella in almond and pistachio.
Introduction
The navel orangeworm, Amyelois transitella Walker (Lepidoptera: Pyralidae) is the primary pest of California almond (Prunus dulcis; 81% of the world supply), pistachio (Pistacia vera; 67% of the world supply) and walnut (Juglans regia) (Statista 2022, Almonds 2023). Currently these crops are planted in > 900,000 ha in California and have a combined annual farm gate value exceeding US $9 billion (Siegel and Gilcrease 2022). This multivoltine moth has a mutualistic relationship with fungal species belonging to the genus Aspergillus that produce aflatoxins, consequently feeding causes direct damage to the nuts and can cause secondary fungal infection (Palumbo et al. 2014; Ampt et al. 2016; Picot et al. 2017; Bush et al. 2018).
Monitoring for A. transitella is important because damage in almonds and pistachios results from a complex interplay of crop phenology and pest population dynamics (Wilson et al. 2020). New crop Nonpareil almonds, the most valuable variety, become vulnerable during hull split (late June–July) when the suture widens exposing the shell and/or nut. The period of vulnerability for Nonpareil almonds typically lasts 5 to 8 weeks until the nuts are shaken from the tree at harvest; the other almond varieties mature from late August through October (Haviland et al. 2022a). New crop pistachios are vulnerable when the hull breaks down after the nut ripens, exposing the split shell for eight to ten weeks from mid-August through mid-October (Haviland et al. 2022b). The value of the damage caused by A. transitella in almonds (goal is damage ≤ 1% assessed at the processor for US Fancy, the highest grade) and pistachios (goal is damage ≤ 1% assessed at the processor) has increased since 2012, due to the combination of increased host availability (currently 628,000+ ha almonds and 196,000+ ha pistachios), increased number of affected nuts, and beginning in 2012, increased heat unit accumulation during the growing season allowing an extra generation to develop each year (Pathak et al. 2021). In some years there are A. transitella outbreaks affecting all nut crops, when average damage increases > fivefold; 2017 was a high damage year for almonds, pistachios and walnuts, with A. transitella damage exceeding 20% in some loads of almonds and pistachios (Siegel 2023). In 2020 almonds contributed $21.5 billion and pistachios contributed $5.2 billion to the California economy (Almonds 2023; AmericanPistachios.Org 2023).
The population dynamics of this moth are complex because it develops on both the new crop and mummies (unharvested nuts from the previous crop) and has different generation times on mummies and new crop nuts, as well as on almond and pistachio (Kuenen and Siegel 2010; Siegel and Kuenen 2011; Siegel et al. 2010). Cohorts developing on mummies and new crop overlap from mid-July through September when the generation time is the shortest due to a combination of rapid degree day accumulation and the high nutritional quality of new crop nuts. This insect was traditionally managed by sanitation, which is the timely removal and subsequent destruction of mummies, and insecticide sprays (Higbee and Siegel 2009, 2012). Mating disruption became available after 2015 (Wilson et al. 2020; Haviland et al. 2021). This moth readily moves between orchards (Andrews and Barnes 1982, Higbee and Siegel 2009, Sappington and Burks 2014, Rovnyak et al. 2018, Reger et al. 2021) and the close proximity of almonds and pistachios in the San Joaquin Valley combined with the different time of crop maturity increases its regional abundance (Wilson et al. 2020).
Monitoring programs for A. transitella were refined in the late 1990s and early 2000s, but subsequently have been in flux due to rapid changes in pest management technology and crop distribution. The earlier programs were based on egg traps (Rice et al. 1976; Van Steenwyk and Barnett 1985) but their use decreased when a pheromone lure became available in 2013 (Leal et al. 2005; Kanno et al. 2010; Kuenen et al. 2010; Higbee et al. 2014). Pheromone lures are still widely used, but mating disruption has become increasingly common and can suppress pheromone traps in orchards as far away as 3 km (Burks 2017). Alternative lures that have been evaluated include oviposition baits (Burks et al. 2011; Nay et al. 2012), a kairomone blend (Burks et al. 2009; Beck et al. 2014) and the non-pheromonal attractant phenyl propionate (PPO), that was identified by mass screening (Price et al. 1967). Phenyl propionate lures are commercially available and capture both sexes and offer a more robust detection in orchards under mating disruption than pheromone lures alone, because there is a synergistic relationship when these two lures are combined (Burks et al. 2016, 2020). Pouches containing ovipositional bait used to trap gravid females are also commercially available and are increasingly used in place of egg traps. These bait pouches generally capture fewer moths than pheromone or PPO (Burks et al. 2009), but a previous study found that female attractants (egg traps or female baits) were more correlated with subsequent damage to Nonpareil almonds than were pheromone traps (Rosenheim et al. 2017).
This paper utilizes data collected from 2020–2023 from a sterile insect technique (SIT) demonstration program, to examine whether the relative effectiveness of these two lures varies with crop (almond or pistachio) and crop phenology, and whether seasonal dynamics (weekly trap catch) was similar or different between the lures. Additionally, since bait traps capture females (> 95%) whereas pheromone + PPO traps capture both sexes, we examined whether the total counts in pheromone + PPO traps paralleled the female-only count. Finally, we conducted a separate experiment to determine if trap proximity affected capture for one or both trap types that were either adjacent to each other or far apart,
Materials and methods
Site description
Trap data from two Nonpareil variety almond orchards (36.327997, − 120.103126; 36.313229, − 120.157808) and two Kerman variety pistachio orchards (36.458726, − 120.102853; 36.356, − 120.048734), 259 ha each, 2–7 km apart, located in western Fresno County, California, 2020–2022, were collected as part of a larger demonstration project for A. transitella SIT. Traps were placed on May 11, 2020 and on January 19 in both 2021 and 2022. Trapping ceased on December 1, 2020, October 11, 2021 and December 15, 2022. In 2023 four new 259 ha pistachio sites were established in western Fresno County and trapping began March 29. All orchards used had active A. transitella management programs including sanitation, trapping and insecticide application.
Traps and lures
Pherocon 1C wing traps (Trece, Adair, OK) were placed in each orchard at a density of one trap per 7.19 ha. The traps were placed on the opposite sides of a designated tree, for a total of 36 traps per lure type, 72 wing traps total per orchard. The sites were approximately 320 m apart, and the outside traps were on the corners and edges of the orchard, with a 4 × 4 grid of traps in the interior of the 259 ha squares. Traps were collected weekly by the California Department of Food and Agriculture (CDFA) Navel Orangeworm Program field staff. Sterile moths were differentiated from wild moths using diet-incorporated dye; moths were crushed to reveal either a pink dyed gut (sterile moth) or non-dyed gut (wild moth). This analysis only used the data for the wild moths. Weekly data were collected as the sum of all traps with the same attractant at the same site; i.e. a sum of 36 ovibait traps and of 36 PPO-pheromone traps for each of the pistachio and almond sites. The trapping data (2021–2023) are reported on a website maintained by CDFA, https://www.cdfa.ca.gov/plant/ipc/nowp/index.html.
Lure types used
The traps used either a combination of two synthetic lures, or a lure based on natural products (Burks et al. 2020). The synthetic lures consisted of a PPO lure (Pherocon NOW PPO-HR L2, Trece, Adair, OK) and a pheromone monitoring lure (Pherocon NOW L2, Trece, Adair, OK). This combination of synthetic lures is designated “Combo” in the remainder of the manuscript. The ovibait lures consisted of packets containing a mix of crushed pistachios and almonds that were collected postharvest (Peterson Trap Company LLC, Visalia, CA). This lure is designated “Bait” in the remainder of this manuscript. All lures were replaced monthly and trap liners collected weekly.
Season division
The trapping season was divided into two portions, with the first portion beginning with the first simultaneous catch for both lure types (Julian Date 140/May 19, 2020; Julian Date 53/February 22, 2021; Julian Date 45/February 14, 2022; Julian Date 79/March 20, 2023) and ending on July 21 (Julian date 202; 203 in 2020), and the second portion continuing until the traps were removed for the season. During the first portion, mummies were the predominant host source until there were substantial split Nonpareil almonds available by the beginning of the third week of July. The cutoff July 21 was chosen because moths emerge from the new crop Nonpareil almonds infested in late June from this time onwards (Siegel et al. 2010). During the second portion of the season, the remaining new crop pollinator varieties split as do pistachios, and most A. transitella develop on new crop nuts, although some mummies remain available.
Analysis of trap capture and assessment of the correlation between lure type and adult capture
Differences in the count data for total moths captured by lure type and by portion of the year were assessed using 2 × 2 contingency chi-square analysis. The data were pooled by commodity for analysis for each year. The correlation between female capture for both bait types, as well as female and male capture in traps using Combo lures was assessed using Spearman’s rho, a nonparametric statistic (JMP v 16.2, SAS Institute, Cary, NC). The observational unit (pairs) for correlation analysis was the number of females or males in all traps in individual 259 ha orchards in a monitoring period (generally 1 week).
Effect of proximity on NOW captured in Bait and Combo traps
A randomized complete block experiment designed to examine the effect of trap proximity and bait type on adult capture was conducted from June 6 to August 7, 2023, in a mature pistachio orchard, variety “Kerman”, located 10.6 km south of Kerman, CA (36.1091, − 120.1363). Trees were planted approximately 5 m apart in orchard rows 6 m apart. This secondary study used orange wing traps (Suterra LLC, Bend OR) previously described by Kuenen et al. (2010) and Burks et al. (2020, 2022). Four treatments were examined assessing three trap placements: (1) an isolated Combo trap; (2) an isolated Bait trap; (3) a Combo trap in the same tree as a Bait trap, (4) a Bait trap in the same tree as a Combo trap (the latter two treatments switched trap position in the tree). Orchard rows served as replicate blocks, and the trap positions were 50 m apart, with replicate blocks separated by 60 m. All trap positions were at least 50 m from the edge of the orchard. Ten replicate blocks were used. Treatment differences were examined using a non-parametric Wilcoxon rank sum test, due to heterogeneity between treatment responses. The response variable was the sum of NOW captured in each trap over the two-month time period. Differences between treatments were examined using the Dunn posterior test. The analysis was conducted using R 4.1.2 (R Core Team 2022) and the FSA package (Ogle et al. 2023).
Results
There were 397,808 moths caught in this study from 2020–2022, Table 1. Slightly more males were captured than females: 201,239 compared to 196,479. Most of the males (194,233; 96.52%) were caught using Combo traps while 7006 (3.48%) were caught using Bait traps. In contrast more females (100,532; 51.17%) were caught using Bait traps than Combo traps (95,947; 48.83%). The overall ratio of male to female was 59.3:39.7 for Combo traps and 4.8:95.2 for Bait traps. More than twice as many moths were captured in pistachio (278,492) than in almond orchards (119, 316) during the period 2020–2022 (70:30). In 2023, during the period March 28-July 12, there were 49,638 moths trapped in pistachios (16,707 males and 32,931 females). Bait traps captured 62.5% of the females and Combo traps captured 86.9% of the males.
Comparison of female capture by time period and by lure 2020–2022
In the combined Almond dataset, Table 2, there were slightly more moths caught after July 21 using Bait traps and substantially more moths (61.1%) caught after July 21 using Combo traps. Pooling the data diminished the difference between Bait and Combo traps, because Bait trap capture was substantially greater before July 21 in 2021 and 2022, at 65.4% and 78.9% respectively, while Combo trap capture ranged from 42.7–44.4% during this same period. All of these differences were statistically significant. For the combined data set the chi-square value was 439.1, P < 0.0001, while for the individual years the values were chi-square = 23.2, P < 0.0001; chi-square = 577.6, P < 0.0001; chi-square = 1370, P < 0.0001, for 2020–2022 respectively. Overall, there were 2.2-fold more females captured in Combo traps than Bait traps. In the combined Pistachio dataset, Table 3, during the period before July 21, 87.1% of the females were caught using Bait traps in contrast to 54.6% of the females caught using Combo traps during this same time period, chi-square = 16,602, P < 0.0001. These differences held for all three years and were more pronounced in 2021 and 2022, with chi-square = 289.4, P < 0.0001; chi-square = 13,170, P < 0.0001; chi-square = 811, P < 0.0001, for 2020–2022 respectively. In a reversal from the Almond dataset, there were 2.0-fold more females caught using Bait traps than Combo traps in pistachio.
Correlation between lure type for female capture
There was one strong (≥ 0.7) season-long correlation between Bait and Combo traps for Almond in 2021, and the remaining correlations were moderate but significant at P < 0.005, Table 4. We could not assess the season long correlations in 2023 because Bait traps were discontinued after July 12 because of cost and manpower issues. In the analysis using the first portion of the season (through July 21) the strength of the correlations increased compared to the season-long values, Table 5. There were strong correlations between the two lures for both Almond and Pistachio in 2021, for Almond in 2022, and Pistachio in 2023. The strength of the correlation between lure type also increased for pistachio in 2022 from 0.57 to 0.66, P < 0.0001. There was no correlation between the lures in 2020 for this same time period, probably because of the smaller sample size; there were 8–13 fewer pairs in this dataset. In pistachios in 2023, the correlation between female capture for the two lures was strong, 0.83, 18 pairs, P < 0.0001.
Season-long correlation between male and female capture using Combo lures 2020–2022
All correlations were significant, and four correlations were strong for Almond in 2020 and 2021 and for Pistachio in 2021 and 2022, Table 6. Male and female trap capture by commodity for each year is shown in Figs. 1, 2, 3. There were at least four peaks with more males trapped than females after July 21 in almond and pistachio respectively (male: 38,805, female: 25,423; male: 76,605, female: 24,877). Throughout the season there was a male peak corresponding to every female peak.
Effect of trap proximity 2023
Significantly more A. transitella were captured in Combo than in Bait traps, chi-square = 25.9, df = 3, P < 0.0001, Table 7. However, there was no difference between the number of A. transitella captured in traps with the same bait when isolated or when presented together, indicating that the two trap types behaved independently when placed in the same tree.
Discussion and conclusions
The data set from the SIT demonstration project for navel orangeworm offers an unprecedented opportunity to compare monitoring systems between commodities. These 259 ha orchards were located in areas where mating disruption is frequently used, and one almond orchard employed mating disruption starting 2021. While mating disruption suppresses pheromone traps within the orchard where it is used as well as adjacent orchards (Burks et al. 2017) it does not affect Bait or Combo traps. The four orchards used in this study are typical of Fresno County, because all used insecticide sprays and had a sanitation program, but the consistency of sanitation was not independently verified. This is an area of ongoing research within the SIT pilot project. Trap capture varied by commodity and by year, with more moths caught in the combined dataset for pistachio than in almond, and in the combined dataset there were more than twice as many females captured in pistachio than in almond for both 2021 and 2022. The higher population of A. transitella in pistachios has been previously described and is due to difficulties sanitizing pistachios (Kuenen and Siegel 2010). The dataset for 2020 differs from the two succeeding years and the numbers captured probably would have been larger if the traps had been set up earlier in the season; there is substantial adult emergence through April and early May that was missed in 2020 (Siegel and Gilcrease 2022). The overall differences in trap capture observed most likely reflect a higher population in pistachio orchards, because almonds are both easier to sanitize than pistachios and have an established mummy threshold for management, while pistachios do not. These differences contribute to a greater overwintering carryover and host availability in pistachio (Kuenen and Siegel 2010; Siegel and Gilcrease 2022; Haviland et al. 2022a, b).
We cannot explain the difference in almond and pistachio between the magnitude of female trap capture using Bait lures, nor can we explain the differences in the percentage of females caught by trap type before July 21. This difference in percentage catch is more pronounced when the data for 2020 for almond are excluded, but the pattern of a greater percentage of females caught using Bait than Combo traps before July 21 held every year for pistachio. When total numbers were evaluated, more females were caught with Combo traps after July 21, with the exception of pistachio in 2020. These differences in trap capture before and after July 21 were reflected by the moderate season-long correlations calculated in both commodities.
The reduced effectiveness of egg and more recently bait traps in the second half of the season has been previously described (Rice et al. 1976; Sanderson and Barnes 1990; Burks et al. 2008) and is attributed to competition with the new crop once hull split begins. To our knowledge, this study is the first to document a higher rate of capture of A. transitella in Bait traps in pistachio (87.1% overall) compared to almond (48.7% overall) in the first portion of the season. The population of A. transitella is usually higher in pistachio than in almond (Burks et al. 2008; Higbee and Siegel 2009), but the current observation is about the effectiveness of baits for trapping A. transitella females in pistachio (1.6-fold difference) rather than moth abundance. The observations in the current study are consistent with those in Nay et al. (2012), but in that study the attractants were different mixtures of almond and pistachio meal compared between the two commodities and they did not distinguish between differences in abundance.
If the difference in female capture between Bait and Combo traps after July 21 simply reflected competition between Bait and new crop nuts (Tables 2 and 3), the pattern should be similar between almond and pistachio, especially because new crop nuts are first available in almond. However, the reduction in capture was greater in pistachio. While there are undoubtedly different volatiles that attract gravid females for these two commodities (Beck et al. 2014) further research is necessary to determine if any of the compounds identified using electroantennogram produce the differences observed between female capture in almond and pistachio. If the difference resulted from a reduced preference for Bait lures by moths emerging from new crop nuts instead, most of these adults emerged from almond, (the first adults that developed on new crop pistachios emerge in September), yet the effect was more pronounced in pistachio. We think it is unlikely that these differences in capture were caused by competition between the two lures when both traps were hung from the same tree because we found no position effects, Table 7. An alternate explanation for the difference in female capture between almond and pistachio for Bait lures is that differences in canopy fill and canopy density between the two commodities affect female attraction to the two lures studied. In general, pistachios have a more compact canopy than almonds and pistachio clusters are distributed throughout the canopy, while in mature almonds the nuts are found higher in the canopy (above 3 m). The only thing that is clear-cut is that in pistachio, there was a dramatic drop in Bait trap capture after July 21.
In the plot of flight activity, Figs. 1, 2, 3, there were multiple peaks in both commodities, as well as considerable agreement between male and female peaks in both almonds and pistachios for 2021 and 2022. Some of the dips in trap capture for both sexes were caused by insecticide applications that had adult activity (pyrethroids, chlorantraniliprole, spinetoram). In almonds, insecticides might be sprayed on mummy nuts (unharvested nuts from previous crop year) during the period Julian dates 118–125 (April 28–May 5) and hull split sprays are usually applied to Nonpareil almonds during Julian dates 185–195 (July 4–July 14). In many almond orchards there is a follow-up application 10–14 d after the first hull split application, Julian dates 199–209 (July 18–July 28), and there may be a pollinator variety spray during Julian dates 222–236 (Haviland et al. 2022a). For pistachios, insecticide application usually occurs from Julian dates 235–245 (August 23–September 2), with subsequent applications during Julian dates 274–283 (October 1–October 10) (Haviland et al. 2022b). Additionally, in some years pyrethroid insecticides are applied to both commodities in April and May (Julian dates 90–145; April 31–May 25) to control Hemipteran pests. In this study neither the timing of insecticide applications nor insecticide choice were coordinated among the participating orchards, yet there still was considerable congruency in the peaks for almond and pistachio in 2021 and 2022, Figs. 2, 3. The almond data were consistent for all three years and pistachio data were more variable because female capture was much lower in 2020, Fig. 1; we cannot explain this discrepancy.
Rosenheim et al. (2017) reported that female-specific traps are more associated with subsequent A. transitella damage to Nonpareil almond than pheromone traps that capture males. In their six-year study evaluating damage to Nonpareil almonds they compared the number of males caught in traps baited with unmated females as a pheromone source, females caught in bait traps (with a different formulation and presentation than the present study), and eggs laid in egg traps. The counts of egg traps and the capture of females in bait traps were highly correlated. Rosenheim et al. (2017) concluded that female-based monitoring methods (either egg traps or bait traps) were the most highly correlated with subsequent damage. However, traps containing PPO were not included in their study, therefore the SIT dataset enabled us to compare Bait and Combo lures over a large hectarage and across several years.
With one exception, the season-long correlation for females between Combo and Bait lures was moderate, but when the focus shifted to the period leading up to July 21 for the years 2021–2023, the correlations strengthened. When we shift focus to the Combo traps, there were strong season-long correlations between male and female capture for both commodities, Table 6, Figs. 1, 2, 3. Burks et al. (2020) reported that a high percentage of gravid females are attracted to Combo traps, and we propose that the size of their peak is a surrogate for mating success during that time period. In these three figures the female peaks at Julian dates 190 (July 9), 250–270 (September 7–27) and 280–290 (October 7–17) correspond to tree nut phenology. The peak observed on July 9 coincides with Nonpareil hull split, the peak observed at September 7–27 coincides with both almond pollinator hull split and pistachio hull breakdown, as does the peak at October 7–17.
In this study, traps baited with Combo lures and traps using Bait as an ovipositional attractant had similar profiles. Bait traps were more effective earlier in the season (through July 21), and during this period female capture was strongly correlated between Bait and Combo traps. Traps containing each of these baits can be used in close proximity to the other without affecting trap counts, which increases the ease of using both at the same time, and in the spring bait traps captured A. transitella females more efficiently in pistachios than in almonds. These findings have implications for both commercial orchard management and researchers seeking to determine an economic threshold for A. transitella. From a research perspective, although Bait traps with their higher female capture appear to be the ideal tool for the elusive goal of determining an economic threshold for Nonpareil almonds (whose split begins in late June and continues through mid-July), their performance in pistachios is a concern because of the drop-off in female trapping during late August through October. This is a critical period because both pistachios and pollinator varieties of almonds split and become susceptible to infestation. From a commercial perspective (the customer for most of these traps and lures) trapping is conducted for population monitoring, the timing of pesticide applications and assessment of application efficacy. The effort taken to determine the sex of the moths captured is too time-consuming, giving Bait traps an advantage since they predominantly capture females.
Is one lure superior? Given a limited budget, Bait traps would appear to be an ideal choice because they predominantly capture females (95:5 ratio in this study), eliminating the need to determine the sex of the moths captured, but their efficacy, as measured by both the number of females trapped in almonds and pistachios, as well as the percentage of total females captured, significantly decreased after July 21. In contrast, Combo traps consistently captured females over the entire season and furthermore, female capture was strongly correlated with male capture, enabling an orchard manager to compare Combo data to trapping datasets from previous years that used pheromone lures. A pest control adviser or orchard manager could make a rough estimate of the number of females trapped by taking 30–40% of the weekly Combo trap capture (sex ratio of M:F of 60:40) instead of attempting to determine the sex of the individual moths caught. Given financial/labor constraints, it is unrealistic to expect both trap types to be used for an entire season, and if an orchard manager can only afford one trap type, Combo traps are preferable because they provide the most consistent season-long capture. The sterile insect technique (SIT) demonstration program made this decision after July 2023 because of these reasons. However, as a compromise, both lures can be used to aid in management decisions before July 21 if labor is available.
Availability of data and materials
The 2020 data are available by contacting the corresponding author. The data for the other years are available on https://www.cdfa.ca.gov/plant/ipc/nowp/index.html.
References
Almonds. https://www.almonds.com. Accessed 20 Aug 2023.
Americanpistachios.org. https://americanpistachios.org. Accessed 20 Aug 2023.
Ampt EA, Bush DS, Siegel JP, Berenbaum MR. Larval preference and performance of Amyelois transitella (navel orangeworm, Lepidoptera: Pyralidae) in relation to the fungus Aspergillus flavus. Environ Entomol. 2016;45:155–62.
Andrews KL, Barnes MM. Invasion of pistachio orchards by navel orangeworm moths from almond orchards. Environ Entomol. 1982;11:278–9.
Beck JJ, Light DM, Gee WS. Electrophysiological responses of male and female Amyelois Transitella antennae to Pistachio and Almond host plant volatiles. Entomol Ex Appl. 2014;153:217–30.
Burks CS. Combination phenyl propionate/pheromone traps for monitoring navel orangeworm (Lepidoptera: Pyralidae) in Almonds in the vicinity of mating disruption. J Econ Entomol. 2017;110:438–46.
Burks CS. Comparison of navel orangeworm adults detected with optical sensors and captured with conventional sticky traps. J Agric Eng. 2022;4:523–32.
Burks CS, Higbee BS, Brandl DG, Mackey BE. Sampling and pheromone trapping for comparison of abundance of Amyelois transitella in almonds and pistachios. Entomol Exp Appl. 2008;129:66–76.
Burks CS, Higbee BS, Kuenen PS, Brandl DG. Monitoring Amyelois Transitella Males and Females with Phenyl Propionate Traps in Almonds and Pistachios. Entomol Exp Appl. 2009;133:283–91.
Burks CS, Higbee BS, Siegel JP, Brandl DG. Comparison of trapping for eggs, females, and males of the naval orangeworm (Lepidoptera: Pyralidae) in Almonds. Environ Entomol. 2011;40:706–13.
Burks CS, Kuenen LS, Daane KM. Phenyl propionate and sex pheromone for monitoring navel orangeworm (Lepidoptera: Pyralidae) in the presence of mating disruption. J Econ Entomol. 2016;109:958–61.
Burks CS, Higbee BS, Beck JJ. Traps and attractants for monitoring navel orangeworm (Lepidoptera: Pyralidae) in the presence of mating disruption. J Econ Entomol. 2020;113:1270–8.
Bush DS, Siegel JP, Berenbaum MR. Accelerated development and toxin tolerance of the navel orangeworm Amyelois transitella (Lepidoptera: Pyralidae) in the presence of Aspergillus flavus. J Chem Ecol. 2018;12:1170–7.
Haviland, DR, Baldwin, R, Hembree, K, Michailides, T, Westerdahl, B. Beede, R, Daane, K, Fukuda, T,Kallsen, C, Shrestha, A, Siegel JP, Weinberger G. UC IPM Pest Management Guidelines: Pistachio. UC ANR Publication 3461; 2022b. https://www2.ipm.ucanr.edu/agriculture/pistachio/.
Higbee BS, Burks CS, Larsen TE. Demonstration and characterization of a persistent pheromone lure for the navel orangeworm, Amyelois Transitella (Lepidoptera: Pyralidae). Insects. 2014;5:596–660.
Haviland DR, Rijal JP, Rill SM, Higbee BS, Burks CS, Gordon CA. Management of navel orangeworm (Lepidoptera: Pyralidae) using four commercial mating disruption systems in California almonds. J Econ Entomol. 2021;114:238–47.
Higbee BS, Siegel JP. New navel orangeworm sanitation standards could reduce almond damage. Calif Agric. 2009;63:24–8.
Higbee BS, Siegel JP. Field efficacy and application timing of methoxyfenozide, a reduced-risk treatment for control of navel orangeworm (Lepidoptera: Pyralidae) in almond. J Econ Entomol. 2012;105:1702–11.
Haviland, DR, Symmes, EJ, JE Adaskaveg, Duncan RR, Roncoroni J, Gubler W, Hanson B, Hembree KJ, Holtz BA, Stapleton, J, Tollerup KE, Trouillas F, Zalom F. UC IPM Pest Management Guidelines: Almond. UC ANR Publication 3431; 2022a. https://www2.ipm.ucanr.edu/agriculture/almond/.
Kanno H, Kuenen LPS, Klingler L, Millar J, Cardé R. Attractiveness of a four-component pheromone blend to male navel orangeworm moths. J Chem Ecol. 2010;36:584–91.
Kuenen LPS, Siegel JP. Protracted emergence of overwintering Amyelois transitella (Lepidoptera: Pyralidae) from pistachios and almonds in California. Environ Entomol. 2010;39:1059–67.
Kuenen LPS, McElfresh JS, Millar JG. Identification of critical secondary components of the sex pheromone of the navel orangeworm (Lepidoptera: Pyralidae). J Econ Entomol. 2010;103:314–30.
Leal WS, Parra-Pedrazzoli AL, Kaissling KE, Morgan TI, Zalom FG, Pesak DJ, Dundulis EA, Burks CS, Higbee BS. Unusual pheromone chemistry in the navel orangeworm: novel sex attractants and a behavioral antagonist. Naturwissenschaften. 2005;92:139–46.
Nay JE, Peterson EM, Boyd EA. Evaluation of monitoring traps with novel bait for navel orangeworm (Lepidoptera: Pyralidae) in California Almond and Pistachio Orchards. J Econ Entomol. 2012;105:1335–2134.
Ogle, DH, Doll JC, Wheeler, AP, Dinno, A. Provided base functionality of dunnTest(). FSA: Simple fisheries stock assessment methods; 2023. https://CRAN.R-project.org/package=FSA
Palumbo JD, Mahoney NE, Light DM, Siegel JP, Puckett RD, Michailides TJ. Spread of Aspergillus flavus by navel orangeworm (Amyelois transitella) on almond. Plant Dis. 2014;98:1194–9.
Pathak TB, Mahesh ML, Rijal JP. Impact of climate change on navel orangeworm, a major pest of tree nuts in California. Sci Total Environ. 2021;755:142657.
Picot A, Ortega-Beltran A, Puckett RD, Siegel JP, Michailides TJ. Period of susceptibility of almonds to aflatoxin contamination during development in the orchard. Eur J Plant Pathol. 2017;148:521–31.
Price DW, Mazrimas JA, Summers FM. Chemical attractants for navel orangeworm moths. Calif Agric. 1967;21:10–1.
R Core Team. R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria; 2022. https://www.r-project.org/.
Reger J, Wenger JA, Brar G, Burks C, Wilson H. Evaluating flight performance of mass-reared and irradiated navel orangeworm (Lepidoptera: Pyralidae) for sterile insect technique. J Econ Entomol. 2021;114:1542–8.
Rice RE, Sadler LL, Hoffmann ML, Jones RA. Egg traps for the navel orangeworm, Paramyelois transitella (Walker). Environ Entomol. 1976;5:697–700.
Rosenheim JA, Higbee BS, Ackerman JD, Meisner MH. Predicting nut damage at harvest using different in-season density estimates of Amyelois transitella: analysis of data from commercial almond production. J Econ Entomol. 2017;110:2692–8.
Rovnyak AM, Burks CS, Gassmann AJ, Sappington TW. Interrelation of mating, flight, and fecundity in navel orangeworm females. Entomol Exp Appl. 2018;166:304–15.
Sanderson JP, Barnes MM. Ability of egg traps to detect the onset of second-generation navel orangeworm (Lepidoptera: Pyralidae) moth activity in Almond Orchards. J Econom Entomol. 1990;83:570–3.
Sappington TW, Burks CS. Patterns of flight behavior and capacity of unmated navel orangeworm (Lepidoptera: Pyralidae) adults related to age, gender, and wing size. Environ Entomol. 2014;43:696–705.
Siegel JP. Nut factors associated with navel orangeworm, Amyelois transitella (Lepidoptera: Pyralidae) damage to pistachio (Pistacia vera) in California (2007–2017) and implication for control. J Econ Entomol. 2023;116:882–90.
Siegel JP, Gilcrease G. Augmenting sanitation with insecticides to improve control of navel orangeworm (Amyelois transitella Walker) (Lepidoptera: Pyralidae) in California tree nuts. Pest Manag Sci. 2022;78:2034–42.
Siegel JP, Kuenen LPS. Variable development rate and survival of navel orangeworm (Lepidoptera: Pyralidae) on pistachio. J Econ Entomol. 2011;104:532–9.
Siegel JP, Kuenen LPS, Ledbetter C. Variable development rate and survival of navel orangeworm (Lepidoptera: Pyralidae) on wheat bran diet and almonds. J Econ Entomol. 2010;103:1250–7.
Statista. https://www.statista.com/statistics/933042/global-pistachio-production-by-country/. Accessed 29 Aug 2022.
Van Steenwyk RK, Barnett WW. Improvements of navel orangeworm (Lepidoptera: Pyralidae) Egg Traps. J Econ Entomol. 1985;78:282–6.
Wilson H, Burks CS, Reger JE, Wenger JA. Biology and management of navel orangeworm (Lepidoptera: Pyralidae) in California. J Integr Pest Manag. 2020;25:1–15.
Acknowledgements
We acknowledge Earl Andress, Lauren Murphy, and Cameron Poole for their roles in establishing the demonstration project and collecting the data, and USDA-APHIS-PPQ and the California Department of Food and Agriculture for institutional support of this demonstration project. Mention of trade names or commercial products in this publication is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the U.S. Department of Agriculture. USDA is an equal opportunity provider and employer.
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This research was conducted as part of the normal duties of the authors. United States Department of Agriculture Animal Plant Health Inspection Service provided funds to California Department of Food and Agriculture for trapping navel orangeworm.
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Conceptualization-JPS, CSB, HW; experimental and statistical analysis, JPS, CSB, writing-original draft preparation, JPS, writing review and editing, JPS, CSB, HW. All authors read and approved the final manuscript.
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Siegel, J.P., Burks, C.S. & Wilson, H. Season-long comparison of trap lures for integrated management of the navel orangeworm (Lepidoptera: Pyralidae) in almond and pistachio. CABI Agric Biosci 5, 30 (2024). https://doi.org/10.1186/s43170-024-00236-z
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DOI: https://doi.org/10.1186/s43170-024-00236-z