In order to achieve rapid detection of thiamethoxam residues in mango, cowpea and water, this study modified the screen printed carbon electrode (SPCE) to make a specific molecular imprinting sensor (Thiamethoxam-MIP/Au/rGO/SPCE) for thiamethoxam. An integrated smartphone platform was also built for thiamethoxam residue analysis. The performance of the complete system was analyzed by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The system was then applied for the rapid determination of thiamethoxam residues in water, mango and cowpea samples. The results showed that the molecular sensor showed good linearity in the range 0.5–3.0 μmol/L of thiamethoxam. The detection limit of thiamethoxam was 0.5 μmol/L. Moreover, the sensor had good reproducibility and anti-interference performance. The average recovery rates of the pesticide residues in water, mango and cowpea samples were in the range of 90–110% with relative standard deviations < 5%. The rapid detection system for thiamethoxam residue constructed in this study was simple, reliable, reproducible and had strong anti-interference. It has broad application prospects in the field detection of thiamethoxam residue, and serves as a valuable reference for the further development of rapid detection technology of pesticide residues in the field of environment and food safety.

Imidacloprid is a neonicotinoid insecticide widely used in the production and cultivation of crops. In recent years, the extensive use of imidacloprid in agricultural production has resulted in large amounts of pesticide residues in agricultural products and the environment. Therefore, it is necessary to establish a rapid, accurate, sensitive and convenient method for detecting imidacloprid pesticide residues to ensure the safety of agricultural products and the environment. To clarify how to use the molecular imprinting method for the electrochemical rapid residue detection of imidacloprid. This paper selected reduced graphene oxide and gold nanoparticles as modifiers modified on screen-printed carbon electrodes (SPCE) chitosan as a functional monomer, and imidacloprid as template molecule to prepare molecularly imprinted polymer, and applied this sensor to the residue detection of imidacloprid. The results showed that the concentration of imidacloprid showed a good linear relationship with the peak response current, and the detection limit of imidacloprid was 0.5 μM, while the sensor had good repeatability and interference resistance. The recoveries of imidacloprid spiked on three samples, mango, cowpea and water, were in the range of 90–110% (relative standard deviation, RSD<5%), which proved the practicality and feasibility of the assay established in this paper. The results of this paper can be used as a basis for the research on the detection of imidacloprid pesticide residues in food or environment.

Bactrocera cucurbitae (Coquillett) is an important pest of cucurbit crops and certain vegetables in Asia, the Middle East, Africa and Hawaii. Most studies on B. cucurbitae have focussed on the effects of prolonged high temperature and very few have examined the effects of short-term exposures to high-temperature on behaviour. In this study, short-term of high-temperature treatments of 33°C, 37°C, 41°C and 45°C were maintained for 1-3hr, and long-term, variable high-temperature treatments were established that consisted of experienced one, two and three times high temperatures stages to 31°C, 33°C, 34°C, 35°C, 36°C, 37°C, 41°C and 45°C for 7hr. We compared the effects of the different high temperatures regimes changes treatments on the mating, oviposition and thermotactic taxis of the flies. The results showed that exposure to a 45°C/1hr treatment, delayed both initiation of mating and oviposition for 8 hr relative to the control but mating and was observed 41 times and oviposition 47 times. By comparison, in the control, mating commenced immediately and was observed 38.3 times and oviposition was observed 41.3 times. Under the other treatments, all the indices for the flies declined with the increase in temperature and duration of exposure. Results showed that 1hr of exposure to 45°C significantly stimulated mating, oviposition and thermotactic behaviour of the flies. These results could improve our understanding of the mechanisms responsible for the population dynamics of B. cucurbitae during the high-temperature season.

Cyromazine is an insect growth regulator insecticide with high selectivity and is widely used in the production and cultivation of fruits and vegetables. In recent years, incidents of excessive cyromazine residues in food have occurred frequently, and it is urgent to establish an accurate, fast, and convenient method for the detection of cyromazine residues to ensure the safety of edible agricultural products. To achieve rapid detection of cyromazine residues, we prepared a molecularly imprinted electrochemical sensor for the detection of cyromazine residues in agricultural products. Samples of tomato (Lycopersicon esculentum Miller), cowpea (Vigna unguiculata), and water were tested for the recovery rate of cyromazine. The results showed that the concentration of cyromazine showed a good linear relationship with the peak response current of the sensor developed in this study. The lower limit of detection for cyromazine was 0.5 µmol/L, and the sensor also had good reproducibility and interference resistance. This paper can be used as a basis for the study of methods for the detection of cyromazine residues in edible agricultural products.

Bactrocera cucurbitae is a major pest of fruit and its reproductive capacity is greatly affected by high temperature. Utilizing ovarian dissection and transcriptome to examine the reproductive biology, we determined that the reproductive capacity of this species is enhanced after exposure for 1 h to 45 °C. The total number of eggs, daily number of eggs, preoviposition period and egg-hatching rate of flies exposed to the high temperature treatment were 693 eggs, 20.4 eggs/d, 6 d and 63.5% versus 666 eggs, 9.6 eggs/d, 11.7d and 96.3%, respectively, in control held at 25 °C for 1 h. The egg-hatching rate was lower than in control, but their ovaries matured in only 6 d versus 12 d in the control. Transcriptome sequencing revealed that after exposure for 1 h to 45 °C, 37 °C, 25 °C, a sequence of 14,492,121,840 nucleotide and 46,826 uniques were screened, and six target genes were involved in oviposition. As temperatures increased, expression levels of Vg-1, Vg-2 and JH-epoxide hydrolase-2 initially increased and subsequently decreased, but the expression of Vg-3 continued to increase there-after. The Vg-receptor which first decreased but then increased.