scholarly journals Honey as a bioindicator of environmental organochlorine insecticides contamination

2023 ◽  
Vol 83 ◽  
Author(s):  
M. Attaullah ◽  
M. A. Nawaz ◽  
I. Ilahi ◽  
H. Ali ◽  
T. Jan ◽  
...  

Abstract Honey is a suitable matrix for the evaluation of environmental contaminants including organochlorine insecticides. The present study was conducted to evaluate residues of fifteen organochlorine insecticides in honey samples of unifloral and multifloral origins from Dir, Pakistan. Honey samples (5 g each) were extracted with GC grade organic solvents and then subjected to Rotary Evaporator till dryness. The extracts were then mixed with n-Hexane (5 ml) and purified through Column Chromatography. Purified extracts (1μl each) were processed through Gas Chromatograph coupled with Electron Capture Detector (GC-ECD) for identification and quantification of the insecticides. Of the 15 insecticides tested, 46.7% were detected while 53.3% were not detected in the honey samples. Heptachlor was the most prevalent insecticide with a mean level of 0.0018 mg/kg detected in 80% of the samples followed by β-HCH with a mean level of 0.0016 mg/kg detected in 71.4% of the honey samples. Honey samples from Acacia modesta Wall. were 100% positive for Heptachlor with a mean level of 0.0048 mg/kg followed by β-HCH with a mean level of 0.003 mg/kg and frequency of 83.3%. Minimum levels of the tested insecticides were detected in the unifloral honey from Ziziphus jujuba Mill. Methoxychlor, Endosulfan, Endrin and metabolites of DDT were not detected in the studied honey samples. Some of the tested insecticides are banned in Pakistan but are still detected in honey samples indicating their use in the study area. The detected levels of all insecticides were below the Maximum Residue Levels (MRLs) and safe for consumers. However, the levels detected can cause mortality in insect fauna. The use of banned insecticides is one of the main factors responsible for the declining populations of important insect pollinators including honeybees.

1983 ◽  
Vol 46 (10) ◽  
pp. 893-900 ◽  
Author(s):  
R. FRANK ◽  
H. E. BRAUN ◽  
G. FLEMING

Between 1969 and 1981, 2482 bovine and 554 porcine carcasses were sampled at provincially inspected abattoirs across Ontario. Abdominal fats were composited into 505 bovine and 122 porcine samples for analyses of organochlorine insecticides and industrial chemicals. Mean ∑DDT residues decreased from 257 μg/kg in 1969–70 to 12 μg/kg in 1981 for bovine fats and from 356 μg/kg in 1971–72 to 5 μg/kg in 1981 for porcine fats. Similar decreases in residue levels were observed for PCB. Dieldrin, with lower initial residues (i.e. 33 μg/kg in bovine fat and 12 μg/kg in porcine), decreased an order of magnitude over this same period. All decreases fitted first order logarithmic regression equations. Chloradane and heptachlor epoxide were rarely observed in bovine or porcine fat; however, the incidence in bovine fat increased after 1973 following the removal of aldrin, dieldrin and heptachlor in 1969 for soil insect control and the subsequent increased use of chlordane. Chlordane appeared at low levels (1–2 μg/kg) in bovine fat during the mid 1970s and remained detectable through 1981. Lindane residues in both bovine and porcine fat fluctuated from year to year and appeared to vary with the need to control insect pests. While present (2 to 39 μg/kg) in the early 1970s, lindane residues disappeared by mid 1970 but reappeared in fatty tissues in 1981 (3–13 μg/kg). A limited number of samples were analyzed for organophosphorus insecticides between 1973 and 1980 and residues were occasionally found. In 1981, the analyses became routine and 3.6% of bovine samples were found to contain detectable residues of fenthion; only 2 of 197 bovine samples exceeded the maximum residue levels permitted under the Food and Drug Act.


2013 ◽  
Vol 2 (1) ◽  
pp. 73-81
Author(s):  
Dr. AbdallaA Elbashir ◽  
Hassan Elobid Ahmed

In this a study tomato sampleswere collected from Khartoum, extracted with acetone, dichloromethane and petroleum ether (1:1:1) and cleaned up by florisil column. Malathion quantitative determination is carried out by gas chromatograph-mass spectrometerusing the optimum ionization mode electron ionization (EI). The detection ofmalathionis confirmed by retention time and comparison of primary and secondary ions.Recovery studies   were performed at two spikes (0.5,0.25mg kg-1) fortification levels of malathion and the recovery obtained ranged from 81% to 97%. The method showed good linearity(R²> 0.995) over the range assayed (from 0.05 to 7.0mg L-1) and the calculated limits of detection (LOD) and quantification(LOQ) were0.03 mg kg-1and 0.11 mg kg-1, respectively. These limits  werelower than the maximum residue levels(MRL) established by European legislations (0.5mg kg-1).


EFSA Journal ◽  
2020 ◽  
Vol 18 (8) ◽  
Author(s):  
◽  
Maria Anastassiadou ◽  
Giovanni Bernasconi ◽  
Alba Brancato ◽  
Luis Carrasco Cabrera ◽  
...  

EFSA Journal ◽  
2018 ◽  
Vol 16 (1) ◽  
Author(s):  
◽  
Alba Brancato ◽  
Daniela Brocca ◽  
Chloe De Lentdecker ◽  
Zoltan Erdos ◽  
...  

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