The objective of this work was to assess the lethal concentration and lethal time (LC and LT) of spinosad and spinetoram, combined with different food lures, and their residual effects on South American fruit fly (Anastrepha fraterculus). The toxic baits were offered in eight concentrations (2, 6, 14, 35, 84, 204, 495, and 1,200 mg L-1), combined with the following food lures: 7% sugarcane molasses, 3% Biofruit, 1.5% CeraTrap, 1.25% Flyral, 3% Samaritá Bait, and 3% Samaritá Tradicional; diluted food lures in water were used as controls. The residual effect of the formulations at 96 mg L-1 concentration were evaluated for 21 days and were compared with that of the commercial bait Success 0.02 CB. Both insecticides were toxic to adults of A. fraterculus, and mortality varied with the food lure used. The LC50and LT50ranged from 15.19 to 318.86 mg L-1and from 11.43 to 85.93 hours, respectively. Spinosad was 2 to 36 times as toxic as spinetoram when combined with different hydrolyzed proteins. Toxic baits formulated with spinosad and spinetoram (96 mg L-1) caused mortality equivalent to the one by Success 0.02 CB (90.2%), when assessed on the day of application. Toxic baits formulated with 3% Biofruit + spinosad and 3% Samaritá Bait + spinetoram are effective for managingA. fraterculusand provide up to seven days of residual effect in the absence of rain; however, only Success 0.02 CB caused more than 80% mortality for up to 21 days.
Ceratitis capitata (Wiedemann, 1824) is a significant insect pest of fruits produced worldwide and is capable of causing direct and indirect damage to fruit. Chemical control is the most frequently used management strategy, mainly involving organophosphate insecticides. However, the frequent use of this chemical group has resulted in unacceptable chemical residues on fruits. In this study, the toxicity of 18 insecticides was evaluated in adults and larvae of C. capitata in a laboratory. The organophosphate insecticides chlorpyrifos (Lorsban 480BR), phosmet (Imidan 500WP), and malathion (Malathion 1000EC); the spinosyns spinetoram (Delegate 250WG) and spinosad (Tracer); and the pyrethroid alpha-cypermethrin (Fastac 100SC) caused high mortality (>80%) in C. capitata adults in topical application bioassays and by ingestion when mixed with Biofruit 5% food lures. However, the insecticides chlorfenapyr (Pirate), spinetoram and chlorpyrifos produced a significant reduction in larval infestation of the fruits (67, 74, and 84% larval mortality, respectively). Insecticides based on spinosyns, alpha-cypermethrin, and cyantraniliprole are alternatives that can replace organophosphates in the management of C. capitata in the field.
The use of toxic baits with spinosyns (spinosad and spinetoram), along with the parasitoid Diachasmimorpha longicaudata, is a sustainable alternative for the management of Ceratitis capitata. This study aimed to evaluate the lethal concentration (LC) and lethal time (LT) of spinosad and spinetoram, associated with the food lures sugarcane molasses at 7 %, Biofruit at 3 %, Ceratrap® at 1.5 %, Flyral® at 1.25 %, Isca Samaritá® and Samaritá Tradicional® at 3 %, on C. capitata, under laboratory conditions, as well as their effect, at the concentration of 96 mg L-1, on D. longicaudata. For the lethal time data, mortality was assessed at 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 36, 48, 60, 72, 84 and 96 h after the exposure to the toxic baits. The lowest lethal concentrations (LC50 and LC95), to spinetoram (0.5 mg L-1 and 3.7 mg L-1, respectively) and spinosad (0.8 mg L-1 and 7.8 mg L-1, respectively), corresponded to the association with Samaritá Tradicional® at 3 %. The lowest lethal time (TL50), in hours, for the spinosad insecticide, corresponded to the formulation containing Biofruit at 3 % (6.6), and, to spinetoram, Samaritá Tradicional® at 3 % (7.9). For D. longicaudata, the formulations that caused the lowest mortality corresponded to the association of Biofruit® at 3 % with spinosad (4.7 %) and Samaritá Tradicional® at 3 % with espinetoram (3.5 %). The toxic baits formulated with spinosad and espinetoram, associated with Isca Samaritá® at 3 %, caused a mortality rate of more than 60 % to the parasitoid D. longicaudata.
The lack of standardization of bioassays for the evaluation of toxic bait toxicity on the South American fruit fly, Anastrepha fraterculus (Weidemann 1830), has led to erroneous interpretations of assay results. The objective of this study was to develop a methodology for the standardization and validation of toxicological tests on A. fraterculus toxic bait using the Success™ 0.02CB formulation (80 mg L −1 of spinosad). Anastrepha fraterculus adults, obtained from larvae reared on an artificial diet, showed higher susceptibility (LT 50 = 48.96 h) than adults from larvae reared on cattley guava (LT 50 = 53.83 h) and mango fruit (LT 50 = 53.55 h). Anastrepha fraterculus adults at the age of five (LT 50 = 65.30 h), 15 (LT 50 = 59.01 h), and 30 (LT 50 = 55.53 h) days presented similar toxicity. The consumption of toxic bait (4.74 mg) increased at 15 days, a fact also observed with insects without food deprivation. In addition, the absence of a food source (artificial diet) with the toxic bait significantly reduced adult mortality time by 7 h (LT 50 = 57.42 h). In relation to exposure time, adults exposed to toxic bait for 1 h reduced consumption by 25%; however, they showed the same susceptibility as insects exposed to 2 (LT 50 = 55.72 h), 4 (LT 50 = 57.64 h), and 8 h (LT 50 = 57.76 h). However, with 24 h of food deprivation, they had a higher susceptibility (LT 50 = 46.48 h). Five-day-old A. fraterculus adults fed an artificial diet before being deprived of food for 12 or 24 h, then exposed to toxic bait for 4 h in the absence of a food source, are considered optimum conditions to evaluate the toxicity of toxic bait.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2025 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.