Persistence and risk assessment of spiromesifen on tomato in India: a multilocational study

Supervised field trials were conducted at four different agro-climatic locations of India to evaluate the dissipation pattern and risk assessment of spiromesifen on tomato. Spiromesifen 240 SC was sprayed on tomato at 150 and 300 g a.i.?ha^?1. Samples of tomato fruits were drawn at 0, 1, 3, 5, 7, 10 and 15 days after treatment and soil at 15 days after treatment. Quantification of residues was done on gas chromatograph–mass spectrophotometer in selective ion monitoring mode in the mass range of 271–274 (m/z). The limit of quantification of the method was found to be 0.05 mg kg^?1, while the limit of determination was 0.015 mg kg^?1. Residues were found below the LOQ of 0.05 mg kg^?1 in 10 days at both the doses of application at all the locations. Spiromesifen dissipated with a half-life of 0.93–1.38 days at the recommended rate of application and 1.04–1.34 days at the double the rate of application. Residues of spiromesifen in soil were detectable level (<0.05 mg kg^?1) after 15 days of treatment. A preharvest interval (PHI) of 1 day has been recommended on tomato on the basis of data generated under All India Network Project on Pesticide Residues. Spiromesifen 240 SC has been registered for its use on tomato by Central Insecticide Board and Registration Committee, Ministry of Agriculture, Government of India. The maximum residue limit (MRL) of spiromesifen on tomato has been fixed by Food Safety Standard Authority of India, Ministry of Health and Family Welfare, Government of India as 0.3 μg/g after its risk assessment.     

Metabolic fate of mancozeb in tomato (Lycopersicon esculentum)

The metabolic fate of mancozeb in tomato (Lycopersicon esculentum Mill.) fruits was evaluated. Results indicate rapid dissipation of mancozeb and its metabolic conversion to ethylenethiourea (ETU), the carcinogenic metabolite. Treatment with mancozeb at flowering stage resulted translocation of ETU in newly emerged fruits indicating the systemic nature of ETU. ETU was detected within one hour of final spraying of mancozeb at the doses of 1.5 and 3?kg a.i./ha. The residue level of ETU increased up to 3-day for both the treatments, which then rapidly dissipated to safer metabolite ethyleneurea (EU) and reached the below detectable limit within 25 days. Cooking of fresh tomatoes caused decontamination of mancozeb residues, which was associated with simultaneous increase in ETU residues. The degradation pattern of ETU after application of mancozeb was slower as compared to the spraying of ETU as such on the crop. A pre-harvest interval of 25 days is recommended.     

Chelating resin immobilized sawdust packed chromatographic column: Application to separation and preconcentration of lead ion

Naturally abundant rubber sawdust has been utilized as a stationary support, which after immobilization with a chelating polyelectrolyte (xylenol orange as counterion) gets converted into a suitable column packing material for isolation and enrichment of trace level target analyte, accurately detectable by the technique of differential pulse anodic stripping voltammetry. The sorbent is robust and re-usable in column-chromatography without showing any leaching and interference complications. Its unique lead ion selectivity from multielemental complex matrices (synthetic water sample, blood serum) at optimized column conditions (pH 2.5 and flow rate 0.5?mL?min^?1) mitigates the usual problems of intermetallic and readsorption effects. Effects of flow rate, pH, equilibration time, and other variables are reported. The system has advantageous feature to be used in a single-column ion chromatography with satisfactory performance. A modest attempt has been made to determine lead fractions in human blood serum samples on the bases of selective retention of ionic and labile fractions on complexing resin.     

Green Synthesis of Silver Nanoparticles Using Exopolysaccharides Produced by Bacillus anthracis PFAB2 and Its Biocidal Property

Journal of Polymers and the Environment - Nowadays when control of environmental toxicity is a matter of concern, the focus of the researchers is to find an eco-friendly process. Considering the...     

Surface characteristics of shales and implication on metal sorption

Differences in surface characteristics between alkaline and acidic shales are demonstrated in the present study. The alkaline shales are characterized by convex surface titration profiles, while the acidic shale exhibits a concave titration profile. Analysis of surface functional groups reveal that carboxylic acids predominate in alkaline shales and the acidic shale is characterized by C=S, C=N (pyridine derivative) and urea (C=O) functional groups, while it lacks –COOH group. The close proximity between pH and point of zero charge for the most acidic and alkaline shales indicate that surface complexation may not play a dominant role in sorption when the system pH is controlled by these sediments.