Influence of Tree Size and Application Rate on Expression of Thiamethoxam in Citrus and Its Efficacy Against Diaphorina citri (Hemiptera: Liviidae)

Abstract Neonicotinoids are a key group of insecticides used to manage Diaphorina citri Kuwayama (Hemiptera: Liviidae), in Florida citrus. Diaphorina citri is the vector of Candidatus Liberibacter asiaticus, the presumed causal agent of huanglongbing, a worldwide disease of citrus. A two-season field study was conducted to evaluate the effect of tree size and application rate on the expression of thiamethoxam in young citrus following application to the soil. D. citri adult and nymph abundance was also correlated with thiamethoxam titer in leaves. Tree size and application rate each significantly affected thiamethoxam titer in leaf tissue. The highest mean thiamethoxam titer observed (33.39 ppm) in small trees (mean canopy volume = 0.08 m3) occurred after application of the high rate (0.74 g Platinum 75SG per tree) tested. There was a negative correlation between both nymph and adult abundance with increasing thiamethoxam titer in leaves. A concentration of 64.63 ppm thiamethoxam was required to reach a 1% probability of encountering a flush shoot with at least one adult D. citri, while 19.05 ppm was required for the same probability of encountering nymphs. The LC90 for the field population was 7.62 ppm thiamethoxam when administered through ingestion. Exposure to dosages as low as 7.62 ppm would likely result in sublethal exposure of some proportion of the population, which could exacerbate resistance development. Based on our results, subsequent work should investigate the use of neonicotinoids by foliar rather than soil application to maintain the chemical class in future insecticide management programs in Florida citrus.

2007, Rogers 2012). Because young trees produce attractive flush shoots often throughout the year, they are at high risk of becoming infected with CLas throughout the year (Stansly and Rogers 2006). Insecticides have been important in mitigating CLas infection of young trees, especially before trees reach fruit-bearing age (Rogers 2012). Extension recommendations by the University of Florida suggest a rotation between soil-applied neonicotinoids and non-neonicotinoid foliar sprays to reduce D. citri populations in young tree groves (Rogers 2012, Rogers et al. 2014. Neonicotinoids are within the Insecticide Resistance Action Committee (IRAC) subgroup 4A, and act on the insect nicotinic acetylcholine receptor (nAChR) (IRAC 2017). Neonicotinoids are highly systemic and when applied to the soil, are taken up by the root system, and transported to the foliage via xylem channels (Elbert et al. 2008).
Three neonicotinoid insecticides are currently labeled for use in nonbearing citrus in Florida: thiamethoxam (Platinum 75 SG-Syngenta Crop Protection, Inc., Greensboro, NC), imidacloprid (Admire Pro 4.6F-Bayer CropScience, Research Triangle Park, NC), and clothianidin (Belay 2.13 SC-Valent USA Corporation, Walnut Creek, CA). Between 6 and 11 wk of D. citri control have been documented following the application of neonicotinoids to the soil (Qureshi and Stansly 2007, Qureshi and Stansly 2009, Ichinose et al. 2010, Rogers 2012. Residual activity of insecticides applied to the soil are likely influenced by factors such as soil type, application volume, irrigation, tree age and size, and environmental conditions such as rainfall. Moreover, neonicotinoid insecticides metabolize into various analytes, though the effect of any one resulting metabolite on D. citri mortality is unknown (Byrne et al. 2017). For example, thiamethoxam metabolizes into clothianidin (Nauen et al. 2003) and clothianidin further metabolizes into TZNG (N-(2-chlorothiazol-5-ylmethyl)-N-nitroguanidine) and TZMU (N-(2-chlorothiazol-5-ylmethyl)-N-methylurea) (Kim et al. 2012). Nevertheless, to date, there has been scant information on movement, distribution, and persistence of soil-applied neonicotinoids or metabolites in citrus tissue in the field.
Previous insecticide trials evaluating soil-applied neonicotinoids used percent control relative to the untreated check or mean number of D. citri per sample size to assess efficacy (Qureshi and Stansly 2007, Qureshi and Stansly 2009, Ichinose et al. 2010, Byrne et al. 2012, Rogers 2012. Additional studies specifically quantified the concentration of neonicotinoids in leaf tissue following soil application using enzyme-linked immunosorbent assay (ELISA) (Castle et al. 2005, Garlapati 2009, Byrne et al. 2017. However, only one attempted to compare percent control with chemical titer within citrus leaf tissues. The lethal concentration of imidacloprid for D. citri was estimated between 200 and 250 parts per billion (ppb) by correlating percentage control of D. citri with imidacloprid titer . Because virtually all D. citri in Florida are assumed to be CLas positive, growers cannot tolerate any feeding on uninfected trees. In 2013, an estimated 1-3% of trees succumb to HLB infection annually in Florida groves, despite deliberate use of soil-applied neonicotinoids (Rogers 2013). Langdon and Rogers (2017) found that 62.19 ppm of imidacloprid was required to kill 90% of D. citri from a laboratory susceptible (LS) population through ingestion and hypothesized that the 200-250 ppb efficacy threshold set by Sétamou et al. (2010) may have been the result of sublethal feeding deterrence as opposed to lethal activity. Nevertheless, uneven uptake or distribution of neonicotinoids in citrus tissue may also result in exposure of D. citri to sublethal doses (Boina et al. 2009, Rogers 2012, which may aid in development of resistance to this particular chemistry. The problem of uneven distribution is compounded as trees grow, requiring increasing application rate. As rates are increased to match tree age and size, annual use limits become increasingly restricting for the development of effective year-long management strategies. Resistance to neonicotinoids was discovered in the field in 2009 (Tiwari et al. 2011a); however, reversion to susceptibility was reported by 2014 (Coy et al. 2016). This was attributed to increased rotations with foliar applied insecticides through area-wide spray programs. A more thorough understanding of the use of soil-applied neonicotinoids and factors that may stimulate the development of resistance is critical to maintaining effective use of this mode of action for management of HLB in Florida citrus.
The purpose of this study was to (i) quantify thiamethoxam expression over time within citrus tissue following soil application, (ii) evaluate efficacy of Platinum 75SG applied at two rates to young citrus trees of two sizes against D. citri, and (iii) quantify susceptibility of the D. citri field population to thiamethoxam by exposure through ingestion. By quantifying the temporal distribution of thiamethoxam in citrus leaf tissue with distinct tree sizes and application rates, we can more effectively refine management recommendations for the use of neonicotinoids in young citrus within the context of resistance management.

Insecticide Application and Citrus Leaf Sampling
A two-season field study was conducted during 2016 and 2017 to determine the concentration of thiamethoxam and resulting metabolites in citrus leaves over time following application of Platinum 75SG to the soil, based on application rate and tree size. We also determined the influence of thiamethoxam concentration on incidence and abundance of D. citri on treated trees over time. Untreated citrus (v. Hamlin/r.s. Swingle) trees of two nonbearing size classes were used in the study and defined as: large (mean canopy volume [MCV] approx. 1.34 m 3 ) and small (MCV approx. 0.08 m 3 ) in size. Large trees used in the study were field planted on 16-III-2015 and small trees were field planted on 01-VIII-2016. The same cohort of large and small trees was used during 2016 as used during 2017. Trees were planted to sandy soil comprising 96.8% sand, 1.6% silt, and 2% clay, with 1.04% organic matter and cation exchange capacity (CEC) of 6.7 meq/100g. Although rate calculations were based on the most common plant density of 140 trees per acre, due to space constraints, trees for this study were planted using a 2.4 m in-row spacing and 2.4 m between-row spacing, which provided sufficient separation to eliminate uptake of insecticides applied to an adjacent tree, confirmed by analysis of trees in the untreated control. The study was arranged in a randomized complete block design with six treatments and four replicates and each plot consisted of four trees. Prior to each insecticide application, tree canopy volume was measured, but no attempt was made to account for differences in individual tree size when identifying treatment plots. The first season insecticide application was made on 8-IX-2016 and the second season application was made on 20-I-2017. At the time of application, 237 ml of insecticide solution (deionized water + insecticide) was applied to the soil at the base of each tree trunk, which is the common application volume in the commercial setting. The high application rate was 0.74 g Platinum 75SG per tree (equiv. 3.67 oz wt product/ac on 140 trees/ac) and the low application rate was 0.37 g Platinum 75SG per tree (equiv. 1.83 oz wt product/ac on 140 trees/ ac). Leaf tissue samples were collected prior to the application of insecticides and then weekly for 12 wk following the application. At each sample date, four mature, fully expanded leaves (~5-15 g) were randomly harvested from the outer canopy across each of the four trees within a plot. Leaves were placed into labeled paper bags and collectively stored by treatment in a plastic re-sealable bag at −20°C until residue analyses were conducted. Additionally, trees were evaluated weekly for the incidence and abundance of D. citri nymphs and adults. At each sample date, the number of D. citri nymphs and adults across 10 flush terminals per plot, and the number of nymph and adult infested terminals within each plot were counted and reported separately.

Extraction and Leaf Tissue Analysis
Leaf material from each plot was ground to fine powder using liquid nitrogen with mortar and pestle. A ~5 g subsample of leaf powder was weighed and transferred to a 20 ml glass vial with a Teflonlined cap and stored at −20°C until extraction; the exact weight of each sample was recorded for conversion of analyte concentration to fresh leaf weight. Extraction was conducted with QuEChERS (Anastassiades et al. 2003) in 15 ml acetonitrile using preweighed reagent sachets (United Chemical Technologies, #ECQUEU7-MP). A cleanup step was then conducted in which chlorophyll was removed from the acetonitrile extract using ChloroFiltr polymeric based sorbent tubes (United Chemical Technologies, Horsham, PA, # ECMPSGG15CT). The supernatant from cleanup was filtered through a 20 µm Teflon filter into an auto sampler vial. Separation and quantification of analytes was accomplished using Ultra-High Performance Liquid Chromatography with a C-18 column coupled to a Thermo TSQ Quantum mass spectrometer (UHPLC-MS). The LOQ was 5 ng/g for imidacloprid, 10 ng/g for clothianidin, thiamethoxam, and 5-OH, and 25 ng/g for olefin, TZMU, and TZNG. The LOD was 1.5 ng/g for imidacloprid, 3.2 ng/g for clothianidin and thiamethoxam, 3.0 ng/g for 5-OH, 8.0 ng/g for olefin, and 8.3 ng/g for TZMU and TZNG. The aqueous mobile phase was 0.1% formic acid in water and the polar modifying phase was 0.1% formic acid in acetonitrile. Samples were run against standards to construct a five-point linear curve in a concentration range of 0.5-50 ppm, and then against a five-point standard curve in the range of 5-300 ppb. The concentration represented by the curve (in extract solution) was then converted back to micrograms/gram leaf tissue using the exact sample weight. The standards were matrix matched to compensate for signal suppression effects of the matrix. Plant tissue free of all four analytes was extracted using QuEChERS as outlined above in order to obtain a blank matrix for mixing working standards. Primary standards were made using technical grade material (97.6-99.9%) in acetonitrile; technical grade material was obtained from Syngenta Crop Protection, Inc., Greensboro, NC, or Valent USA Corporation, Walnut Creek, CA). A set of working standards encompassing the linear range of concentrations was prepared from the primary standards, again in acetonitrile. To prepare a range of working standards in blank plant matrix, a 1,000 µl aliquot of blank plant matrix was dry evaporated under nitrogen. The residue was then reconstituted with a 1,000 µl aliquot of standard acetonitrile. The solution was sonicated to ensure a homogeneous product and passed through a 0.2 µm PTFE filter prior to injection, as were unknowns.

Lab Culture
The LS strain was reared in continuous culture at the University of Florida Citrus Research and Education Center in Lake Alfred on Murraya koenigii maintained at 27°C with RH 65% with a photoperiod of 14:10 (L:D) h. The colony did not receive any exposure to insecticides following establishment in 2005 and routine quantitative real time (qPCR) testing as described in Pelz-Stelinski et al.
(2010) was used to confirm the colony was CLas-free. Adult D. citri were aspirated from host rearing plants and used in laboratory bioassays during the same day to reduce unintended mortality.
Field Collection of D. citri D. citri adults were collected prior to the first field application to establish baseline susceptibility of the field population to thiamethoxam in the laboratory. Adults were aspirated from citrus foliage in the field and transported to the lab within labeled plastic aspirator vials. Laboratory assays were conducted during the same day that D. citri were collected from the field to reduce unintended mortality.

Ingestion Bioassay
The ingestion assay was comprehensively described in Langdon and Rogers (2017). Briefly, a 30% sucrose solution was used as the base artificial diet. Serial dilution was conducted to form eight doses of spiked diet using formulated Platinum 75SG (750 g thiamethoxam kg, Syngenta Crop Protection, Greensboro, NC). The caps of 5 ml snap-cap centrifuge tubes (Eppendorf Tubes, Hamburg, Germany, Cat. No.: 0030119401) were filled with 0.7 ml of each prepared dose. Parafilm M (Bemis, Neenah, WI, Cat. No.: PM-992) was stretched over each diet-filled cap. Four to six adult D. citri were loaded into each centrifuge tube and the diet-filled cap was reinstalled. Tubes were held upright in a tube tray at 27°C, 70% relative humidity, with a 14:10 (L:D) h photoperiod for 72 h. One replicate was defined as a single tube and 10 replicates were used for each dose. Between 40 and 60 adults were tested for each dose. After 72 h, insects were scored as alive (full function), moribund (insects lacking coordinated movement), or dead (no movement upon disturbing). Moribund insects were classified as dead for data analysis.

Statistical Analyses
Chemical titer data were averaged over replicate and subjected to a general linear mixed model using SASv9.4 (Proc GLIMMIX, SAS Institute 2013) to test for year by treatment interactions. Means were square root transformed prior to analysis to achieve homogeneity of variance meeting the assumptions of the model, as checked by visual examination of the residuals to ensure constant variance and normality. Additionally, chemical titer data were averaged over replicate and year and subjected to a general linear mixed model using SASv9.4 (Proc GLIMMIX, SAS Institute 2013) to test for tree size by application rate interactions. Means were square root transformed prior to analysis to achieve homogeneity of variance and meet the assumptions of the model. For tests of differences between treatments, data were subjected to a nonparametric multiple comparisons test where mean separations indicate differences between treatments within the same sample week at α ≤ 0.05.
Insect count data were in monotonic distribution; therefore, data were subjected to Spearmans rank-order correlation using JMP (JMP Version 13, SAS Institute 2007) to determine if concentration of thiamethoxam, or the metabolites clothianidin, TZNG, or TZMU influenced D. citri incidence on leaves. Correlations were estimated using the Restricted Maximum Likelihood (REML) method. Additionally, nymph and adult incidence data were subjected to Probit analysis using SAS v9.4 (Proc Probit, SAS Institute 2013) to determine the probability of encountering a flush terminal containing at least one nymph or one adult based on thiamethoxam titer.
The high rate (0.74 g Platinum 75SG per tree) applied to the small tree size resulted in the highest thiamethoxam titer observed during each week following application; the peak mean concentration occurred 2 and 3 wk following the application of 33.39 and 33.29 ppm of thiamethoxam, respectively (Table 1). Mean thiamethoxam titer peaked at 12.53 ppm by 3 wk after the application of the low rate application (0.37g) of Platinum 75SG per small tree; however, no significant difference in titer was observed between rates in small trees 3 wk following application (χ 2 = 36.53, P < 0.0001, Table 1). Peak thiamethoxam titer was observed at 2 (2.86 ppm) and 4 (2.47 ppm) wk after the high rate (0.74 g Platinum 75SG per tree) application to large trees, and at 2 wk (0.69 ppm) following the low rate (0.37 g Platinum 75SG per tree) application to large trees. At 2 and 4 wk after application, significantly more thiamethoxam was found after the high rate than the low rate application to large trees (χ 2 = 40.27, P < 0.0001 and χ 2 = 43.91, P < 0.0001, respectively, Table 1).
The thiamethoxam metabolite, clothianidin, peaked at 5 wk post application of both the high rate (15.44 ppm) and the low rate (6.29 ppm) of Platinum 75SG in trees of small size (Table 2). Following application to the large size trees, clothianidin titer peaked at 4 wk with both the high rate (1.69 ppm) and the low rate (0.48 ppm). Very low levels (<2 ppm) of the clothianidin metabolites, TZMU (Table 3) and TZNG (Table 4) were detected in leaf tissues from trees following the application of Platinum 75SG to the soil.

Baseline Susceptibility of Field D. citri Population
The lethal concentration required to kill half of the field-collected (Vero Beach) population (LC 50 ) by ingestion was 0.20 ppm of thiamethoxam, while the LC 50 was 0.11 ppm for the lab susceptible population (Table 5). A comparison of these results indicates that the field population investigated during this experiment was fully susceptible to thiamethoxam, exhibiting a resistance ratio (RR 50 ) of 1.82. Furthermore, the lethal concentration required to kill 99% of the field-collected population by ingestion (LC 99 ) was 147.91 ppm thiamethoxam.
Approximately 5 wk of nymph and adult control was observed in 2016 and 2017 ( Fig. 2A and B, respectively), following application of the low rate of Platinum 75SG to the soil beneath small trees, where 'control' is defined as 100% compared with the untreated check. In contrast, 10 and 9 wk of nymph and 8 and 7 wk of adult control was observed in 2016 (Fig. 2C) and 2017 (Fig. 2D), respectively, following the high rate application to trees of the small size. The low rate applied to the large tree size did not offer complete  control of nymphs or adults at any time during 2016 or 2017 ( Fig. 3A and B, respectively). During 2016, complete adult control was observed only during weeks 1 through 3 following the high rate application to trees of the large size (Fig. 3C), but the same level of adult control was not observed during 2017 (Fig. 3D); nymph control reached 100% only at 2 wk after application in 2016 (Fig. 3C).

Discussion
The goals of this study were to: i) quantify uptake and expression of thiamethoxam in young citrus trees of two sizes following the application of Platinum 75SG to the soil at two rates; ii) evaluate residual efficacy against D. citri nymphs and adults; and iii) quantify the susceptibility of the field population of D. citri to thiamethoxam by comparing lethal concentration values with vector control as determined by population monitoring. This was the first formal investigation to use UHPLC-MS for quantification of the four analytes of Platinum 75SG (thiamethoxam, clothianidin, TZNG, and TZMU) in citrus leaf tissues following soil application in the field. Thiamethoxam is a neonicotinoid precursor to clothianidin (Nauen et al. 2003) and clothianidin is known to metabolize into TZNG and TZMU (Kim et al. 2012). While clothianidin is effective against D. citri, little is known about the influence of specific dosage on D. citri feeding behavior or mortality (Byrne et al. 2017). Langdon and Rogers (2017) found that the LC 50 of thiamethoxam and clothianidin to the LS population by ingestion was 0.11 and 0.09 ppm, respectively, while the LC 90 was 4.94 and 9.35 ppm, respectively. Because a higher dose of clothianidin was required to achieve the same level of mortality at the 90% lethal concentration, it is unlikely that mortality observed in the current study is the result of exposure to the metabolite, clothianidin alone. Furthermore, the concentration of each of the three metabolites is directly dependent upon the concentration of thiamethoxam. Consequently, we cannot determine how any one metabolite, including clothianidin, affects D. citri mortality in this study. While understanding the role of each metabolite is beyond the scope of this investigation, it is possible that the combination of multiple metabolites has an additive effect on D. citri mortality as suggested by Byrne et al. (2017). Byrne et al. (2017) demonstrated a strong correlation between thiamethoxam and the metabolite, clothianidin, but were unable to determine whether mortality was the result of either thiamethoxam or clothianidin, or a combination of the two. Although earlier studies used ELISA to quantify expression of neonicotinoids (Castle et al. 2005, Garlapati 2009), they did not quantify metabolites of thiamethoxam nor manipulate tree size or application rate to study effects on thiamethoxam titer. The target concentration threshold of imidacloprid following application to the soil was 200-250 ppb based on the report by Sétamou et al. (2010). Since a correlation between D. citri abundance and clothianidin or thiamethoxam titer did not exist, 200-250 ppb became the assumed efficacy threshold concentration for all neonicotinoids (K.W.L., personal observations). In the current investigation, peak levels of nearly 3 ppm (3000 ppb) and 0.7 ppm (700 ppb) of thiamethoxam were measured when the respective high and low rates tested were applied to trees of the large size. When the high and low rates were applied to trees of the small size, peak concentrations were nearly 18-and 11-fold higher, respectively, than when applied to the large tree size. Each titer was well above the 250 ppb upper threshold set for imidacloprid, suggesting that efficacy should be expected in both tree sizes at the rates tested. However, despite the high titers observed in our study, we failed to reach a mean dose high enough to provide a 95% confidence (34.40 ppm) of only a 1% probability of encountering a flush shoot with at least one adult D. citri. We did, however, observe a mean concentration high enough in only the small tree size at both rates, to achieve a 95% confidence (12.17 ppm) of only a 1% probability of encountering a flush shoot with at least one nymph, albeit that titer was reached only during the third week of the investigation in the low rate treatment; the high rate treatment exceeded 12.17 ppm between weeks 1 and 6.
The LC 90 for the field population was 7.62 ppm. This was exceeded during the first 3 wk after the low rate was applied to trees of the small size and was exceeded for the first 7 wk after the high rate was applied to trees of the small size. Given that nearly 100% control of adults was observed for up to 8 wk following application of either rate to the small tree size, it is possible that dosages as low as 7.62 ppm are capable of deterring some proportion of D. citri from feeding and, therefore, may offer nonlethal control of D. citri in young citrus trees. Electropenetrography was used to demonstrate that imidacloprid applied to the soil in the greenhouse can reduce phloem feeding by D. citri; however, phloem feeding was not prevented in either study (Serikawa et al. 2012, Miranda et al. 2016). The rate of imidacloprid applied to the soil in each study was known, but the imidacloprid titer within the phloem sap was unknown. Langdon and Rogers (2017) defined insecticide-mediated feeding deterrence of D. citri as 'gustatory avoidance of less or nonsuitable feeding sources.' As adults search for a suitable host plant and are exposed to citrus tissue containing more than 7.62 ppm of thiamethoxam, adults may move to find a leaf containing a lower concentration within the same plant or move to a new host plant that contains a concentration sufficiently low to be suitable for feeding. This movement away from the treated foliage or tree may result in a perception of control upon visual assessment, but should not be confused with mortality. Survival of exposed insects may promote the development of resistance to thiamethoxam and likely other chemistries within the same mode of action in populations of D. citri. Thiamethoxam is known to metabolize into clothianidin, which acts on the same receptor site as imidacloprid (Nauen et al. 2003), supporting a high likelihood of cross-resistance. Imidacloprid resistant D. citri express higher levels of detoxifying enzymes, including general esterase, glutathione S-transferase, and cytochrome P 450 monooxygenases (Tiwari et al. 2011a). Reduced penetration, target-site insensitivity, and mutations in detoxifying enzymes may also play a role in resistance (Tiwari et al.  2011a). Tiwari et al. (2011b) found five family 4 cytochrome P 450 genes induced by imidacloprid exposure. Imidacloprid and thiamethoxam are within the same chemical subgroup (4A); therefore, cross-resistance between the two chemistries is of concern. Additionally, thiamethoxam persisted at very low levels (~0.05-0.80 ppm) during the final evaluation of this investigation (12 wk following application). The duration at which sublethal doses in this range will persist is unknown; if doses in this range do not inhibit feeding activity, it may further increase the likelihood and rate of resistance development.
D. citri resistance to neonicotinoids has been recently documented in Florida (Tiwari et al. 2011a, Kanga et al. 2016); therefore, a deeper understanding of soil-applied neonicotinoids was warranted for development of future resistance management strategies. We observed a number of effects that are of significant concern regarding use of neonicotinoids by soil application in Florida citrus: i) failure to achieve lethal concentrations in leaf tissue following application to the soil; ii) persistence of thiamethoxam concentrations at low levels (less than 1 ppm) through 12 wk following application; and iii) failure of the highest allowable annual rate to achieve acceptable D. citri control following application to trees 18 mo of age (MCV = 1.34 m 3 ). Resistance management is critical for neonicotinoid stewardship to ensure implementation of the chemical class in future citrus production. Therefore, the current results suggest that application of neonicotinoids to the soil, particularly in trees with a developed canopy (those greater than 18 mo), may result in neonicotinoid titers that cause selection pressure for evolution of resistance in current populations of D. citri in FL. The significant reduction in titer between small trees and large trees after soil application may simply be a result of dilution of chemical due to an increase in canopy size, application method in relation to root distribution under the canopy, or perhaps due to compromise of the root system caused by CLas infection resulting in reduced uptake of available compound. If the latter is true, soil-applied neonicotinoids may work better when applied to trees not compromised by HLB. Because the trees used in this study were insecticide-free prior to each application, it is likely that all trees, particularly of the large size, had some level of CLas infection, which may have negatively influenced uptake efficiency. As an alternative to soil-applied neonicotinoids, subsequent investigations should evaluate foliar neonicotinoid applications for management of nonbearing citrus and resulting coverage uniformity, peak residue levels, degradation over time, and efficacy.
Follow-up comparative investigations quantifying the concentration of thiamethoxam, imidacloprid, and clothianidin required to interrupt and manipulate feeding behavior of D. citri that utilize electropenetrography are warranted to further improve the use of these management tools for D. citri and HLB in citrus. Moreover, alternative soil application methods should be investigated that attempt to increase uptake efficiency, particularly in trees 18 mo and older. Given the dynamic nature of susceptibility of D. citri to insecticides, we must remain diligent in research efforts with a keen focus on resistance management and be willing to adjust insecticide use patterns to ensure the longevity of each available chemical class.

Supplementary Data
Supplementary data are available at Journal of Economic Entomology online.