Assessment of chromium, lead and mercury in seawater and some fish species from the Gulf of Urabá, Colombian Caribbean: a baseline study.

The coastline of the department of Antioquia, in Colombia, exhibits a wide variety of aquatic and land ecosystems rich in both diversity and abundance. However, it is exposed to a variety of human activities, including industry, tourism, and mining. Banana cultivation is the main activity carried out in this region, which offers large economic benefits. In addition, there are diverse fishery resources that are main basis of the economy and nutrition for the population. Over the years, the Gulf of Urabá has been affected by serious pollution problems due to elevated contents toxic compounds that deteriorate the aquatic ecosystem, even our laboratory has conducted previous studies in heavy metals in fish from this same area. The aim of this study was to evaluate the contents of chromium (Cr), lead (Pb), and mercury (Hg) in seawater and fish muscle in three fish species from the Gulf of Urabá that are commercialized and consumed by the population of the municipality of Turbo, using microwave-induced plasma optical emission spectrometry (MIP OES). The occurrence of toxic metals in seawater in this area has not been reported, and to the best of our knowledge, this is the first study. Cr and Pb concentrations in seawater from several sampling points were detected ranged from 0.025 to 0.369 mg/L and 0.012-0.165 mg/L, respectively, while Hg levels were below detection limit. Regarding fish samples, Pb and Hg levels range 0.64-1.91 mg/kg and 0.11-1.09 mg/kg, respectively. Sea catfish species exhibited the highest content of metals, followed by stone head catfish and anchovy, it which showed the lowest contamination by metals. In this study, levels that exceed the limits in Colombian regulations regarding metal contents in discharge points to surface water and fishery products for human consumption were found.

Polycyclic Aromatic Hydrocarbons in Surface Sediments and Fish Tissues Collected from a Protected Lagoon Region.

Polycyclic aromatic hydrocarbons (PAHs) were detected and quantified in sediment and edible fish (Megalops atlanticus) from Caleta lagoon (Lagoon of Terminos, Mexico) in order to assess their potential health impact on consumers. Sum PAH concentrations in sediment and fish muscle tissues were dominated by high molecular weight PAH compound (46.4%-93.1%) relative to low molecular weight compounds (6.9%-42.9%). Contamination was associated with local industrial activities and urbanization. The effective range low (ERL: 4022 ng g-1) value were lower suggested adverse biological effect would be rarely observed. While the analysis of PAHs in muscle of M. atlanticus suggests a minimum impact to consumers according to the permitted limits of dibenzo (a, h) anthracene (10 ng g-1) and benzo [a] pyrene (0.1-1.2 µg kg-1). It is advisable to propose environmental strategies to mitigate future environmental damage in the ecosystem.

Determination of multiclass, semi-polar pesticide residues in fatty fish muscle tissue by gas and liquid chromatography mass spectrometry.

With the aim of monitoring multiclass semi-polar pesticide residues in freshwater fatty fish, two QuEChERS approaches (so-called acetate buffered and unbuffered versions) were evaluated for the determination of 77 pesticide residues. Compounds were selected according to the dominant rainfed agriculture activities in South America. Unbuffered QuEChERS was finally chosen for validation purposes owing that it provided the best results in terms of recovery yields. Method performance was evaluated in two instrumental systems, liquid chromatography - tandem mass spectrometry (LC-MS/MS) in Scheduled MRM™ algorithm available on hybrid quadrupole - linear ion trap (QLIT) instrument, and gas chromatography - mass spectrometry (GC-MS) under selected ion monitoring (SIM) mode. Spiking experiments were carried out to determine the trueness, precision, linearity, limit of quantification of the method as well as matrix effect. The Unbuffered QuECHERS method described here: •Was validated for the analysis of 67 pesticide residues in fish muscle tissue.•Presented quantification limits in the range 1-15 µg kg-1 for the vast majority of the studied compounds.•Enable environmental monitoring of pesticide residues in fish due to their low LOQs.

Development, validation and matrix effect of a QuEChERS method for the analysis of organochlorine pesticides in fish tissue.

This study aims to develop and validate a method to determine OCPs in fish tissues, minimizing the consumption of sample and reagents, by using a modified QuEChERS along with ultrasound, d-SPE and gas chromatography with an electron capture detector (GC-ECD), refraining the pooling. Different factorial designs were employed to optimize the sample preparation phase. The validation method presented a recovery of around 77.3% and 110.8%, with RSD lower than 13% and the detection limits were between 0.24 and 2.88 µgkg-1, revealing good sensitiveness and accuracy. The method was satisfactorily applied to the analysis of tissues from different species of fish and OCPs residues were detected. The proposed method was shown effective to determine OCPs low concentrations in fish tissues, using small sample mass (0.5 g), making the sample analyses viable without the need for grouping (pool).

Optimization of an acid digestion procedure for the determination of Hg, As, Sb, Pb and Cd in fish muscle tissue.

A simple, efficient and cost effective method was developed and optimized for the digestion of fish tissue for the determination of Lead, Cadmium, Mercury, Antimony, Arsenic and Selenium by FAAS, CVAAS and HGAAS. Three of the more common classical open tubed acid digestion procedures were explored with the purpose of optimizing the variables and selecting the single most efficient, convenient and inexpensive digestion method. The effect of parameters such as digestion media, digestion time and digestion temperature on the efficiency of extraction of heavy metals from fish tissue was examined. Concentrated nitric acid was determined to be the most efficient digestion media for all the metals studied. •Efficient extraction of Arsenic, Selenium, Antimony, Lead and Cadmium was achieved at a digestion temperature of 100 °C for 120 min.•Optimum extraction of Mercury in fish tissue was achieved at 85 °C for 120 min since at higher temperatures, mercury was lost due to volatilization.