Cold Vapor Atomic Fluorescence Spectrometry Research Articles

Analysis of Sources and Sinks of Mercury in the Urban Water Cycle of Frankfurt am Main, Germany

Mercury (Hg) is still a focus of environmental research, since its levels in fish frequently exceed the Environmental Quality Standard (EQS) of 20 µg/kg for biota defined by the European Water Framework Directive (Directive 2008/105/EC). Current Hg levels in Abramis brama from German rivers are in the range of 73–346 µg/kg wet weight (2009) and exceed the EQS by a factor of 3.7–17.3. Therefore, it is important to identify the sources of Hg pollution in the aquatic environment and to develop effective strategies for reducing the input into associated river systems. The aim of the present study was to analyze Hg in the urban water cycle of the city of Frankfurt am Main, Germany. Samples were taken from the river Main crosscutting the city and its tributaries. In addition, precipitation, stormwater runoff, effluents of two municipal WWTPs, and stormwater management structures such as combined sewer overflows and stormwater retention basins have been analyzed. Loads of Hg have been determined based on the measured concentrations and a Hg mass balance for the aquatic system was created. A total of 160 water samples were analyzed by cold vapor atomic fluorescence spectroscopy (CVAFS) according to US EPA Method 1631. Results from the mass balance have shown that approximately 5 kg Hg/a enter and 15 kg Hg/a leave the study area of Frankfurt am Main via the river Main. The largest amount of Hg (24.58 kg/a) throughout the urban water cycle of Frankfurt am Main is transported via wastewater. However, municipal WWTPs in Frankfurt am Main have been identified as the largest Hg sink, since 99.7% (24.5 kg/a) of the Hg is shifted from the sewage water and stormwater during treatment into the sewage sludge. Thus, the increase of the Hg load in the river Main from 5 to 15 kg/a has to be attributed to other sources such as 3 industrial WWTPs, groundwater and non-treated stormwater runoff during heavy rain events.

Nanogold-Decorated Silica Monoliths as Highly Efficient Solid-Phase Adsorbent for Ultratrace Mercury Analysis in Natural Waters.

We propose a novel analytical method for mercury (Hg) trace determination based on direct Hg preconcentration from aqueous solution onto a gold nanoparticle-decorated silica monolith (AuNP@SiO2). Detection of Hg is performed after thermal desorption by means of atomic fluorescence spectrometry. This new methodology benefits from reagent-free, time- and cost-saving procedure, due to most efficient solid-phase adsorbent and results in high sensitive quantification. The excellent analytical performance of the whole procedure is demonstrated by a limit of detection as low as 1.31 ng L(-1) for only one-min accumulation duration. A good reproducibility with standard deviations ≤5.4% is given. The feasibility of the approach in natural waters was confirmed by a recovery experiment in spiked seawater with a recovery rate of 101%. Moreover, the presented method was validated through reference analysis of a submarine groundwater discharge sample by cold vapor-atomic fluorescence spectrometry resulting in a very good agreement of the found values. Hence the novel method is a very promising new tool for low-level Hg monitoring in natural waters providing easy-handling on-site preconcentration, reagent-free stabilization as well as reagent-free, highly sensitive detection.

Levels and potential health risks of mercury in prescription, non-prescription medicines and dietary supplements in Poland

Determination of mercury is important in the case of pharmaceuticals for which the European Union regulations have not defined the maximum permissible concentration of this metal. The aim of the study was to determine the levels of mercury in the following groups of drugs (n = 119): analgesics, diuretics, cardiacs, antihypertensives, anti-influenza, antibiotics, anti-allergics, tranquilizers, antibacterials and in dietary supplements (n = 33) available on the Polish market. Mercury was analyzed using cold vapor atomic fluorescence spectrometry CV-AFS. Its content in the samples varied in the range of 0.9–476.1 ng g−1. Higher mercury concentrations were reported for prescription drugs (Rx): 0.9–476.1 ng g−1 (median: 7.4 ng g−1), lower – for non-prescription medicines (OTC): 1.2–45.8 ng g−1 (median: 6.0 ng g−1). In the analyzed dietary supplements the concentrations were: 0.9–16.7 ng g−1 (median: 5.9 ng g−1). On the basis of the information contained in the leaflet accompanying the medicine, a daily dose of mercury taken into the body with an analyzed medicament was estimated and the health risk posed by using such medicines was assessed. The study indicates that it is justified to carry out measurements of mercury in pharmaceuticals due to its high, potentially harmful.

In situ selective determination of methylmercury in river water by diffusive gradient in thin films technique (DGT) using baker's yeast (Saccharomyces cerevisiae) immobilized in agarose gel as binding phase

Saccharomyces cerevisiae immobilized in agarose gel as binding phase and polyacrylamide as diffusive layer in the diffusive gradient in thin films technique (DGT) was used for selective determination of methylmercury (MeHg). Deployment tests showed good linearity in mass uptake up to 48 h (3276 ng). When coupling the DGT technique with Cold Vapor Atomic Fluorescence Spectrometry, the method has a limit of detection of 0.44 ng L−1 (pre concentration factor of 11 for 48 h deployment). Diffusion coefficient of 7.03 ± 0.77 × 10−6 cm2 s−1 at 23 °C in polyacrylamide gel (pH = 5.5 and ionic strength = 0.05 mol L−1 NaCl) was obtained. Influence of ionic strength (from 0.0005 mol L−1 to 0.1 mol L−1 NaCl) and pH (from 3.5 to 8.5) on MeHg uptake were evaluated. For these range, recoveries of 84–105% and 84–98% were obtained for ionic strength and pH respectively. Potential interference due to presence of Cu, Fe, Mn, Zn was also assessed showing good recoveries (70–87%). The selectivity of the proposed approach was tested by deployments in solutions containing MeHg and Hg(II). Results obtained showed recoveries of 102–115 % for MeHg, while the uptake of Hg(II) was insignificant. The proposed approach was successfully employed for in situ measurements in the Negro River (Manaus-AM, Brazil).

Speciation analysis of mercury in sediments using ionic-liquid-based vortex-assisted liquid-liquid microextraction combined with high-performance liquid chromatography and cold vapor atomic fluorescence spectrometry.

An improved novel method based on ionic liquid vortex-assisted liquid-liquid microextraction has been developed for the extraction of methylmercury, ethylmercury and inorganic mercury in sediment samples prior to analysis by high-performance liquid chromatography with cold vapor atomic fluorescence spectrometry. In this work, mercury species were firstly complexed with dithizone, and the complexes were extracted into 1-hexyl-3-methylimidazolium hexafluorophosphate. Key factors that affect the extraction efficiency of mercury species, such as type and amount of ionic liquid and chelatants, extraction time, sample pH, salt effect and matrix effect were investigated. Under the optimum conditions, linearity was found in the concentration range from 0.1-70 ng/g. Limits of detection ranged from 0.037-0.061 ng/g. Reproducibility and recoveries were assessed by extracting a series of six independent sediment samples that were spiked with different concentration levels. Finally, the proposed method was successfully applied in analysis of real sediment samples. In this work, ionic liquids vortex-assisted liquid-liquid microextraction was for the first time used for the extraction of mercury species in sediment samples. The proposed method was proved to be much simpler and more rapid, as well as more environmentally friendly and efficient compared with the previous methods.

A Metalloproteomics Study on the Association of Mercury With Breast Milk in Samples From Lactating Women in the Amazon Region of Brazil.

This study aimed to identify metalloproteins that lose their metal ions in the presence of mercury (Hg) and bind to Hg in breast milk samples collected from the riverine population of the Madeira River, a tributary of the Amazon River. Initially, total Hg was determined from the hair of lactating women to identify individuals who were contaminated followed by a proteomic analysis of breast milk samples through two-dimensional polyacrylamide gel electrophoresis after acetone precipitation. The presence of Hg in the obtained protein spots was determined by cold vapor atomic absorption spectrometry and cold vapor atomic fluorescence spectrometry. These determinations indicated the presence of Hg in one protein spot, which was then characterized through electrospray ionization tandem mass spectrometry. Based on searches in the UniProt database, this protein spot was identified as lysozyme C.

Mercury(II) trace detection by a gold nanoparticle-modified glassy carbon electrode using square-wave anodic stripping voltammetry including a chloride desorption step

Gold nanoparticles (AuNPs) were deposited on a glassy carbon (GC) substrate by constant potential electrolysis and characterized by cyclic voltammetry in H2SO4 and field emission gun scanning electron microscopy (FEG-SEM). The modified AuNPs–GC electrode was used for low Hg(II) concentration detection using a Square Wave Anodic Stripping Voltammetry (SWASV) procedure which included a chloride desorption step. The comparison of the obtained results with our previous work in which no desorption step was used showed that this latter step significantly improved the analytical performances, providing a three time higher sensitivity and a limit of detection of 80pM for 300s preconcentration, as well as a lower average standard deviation. The influence of chloride concentration on the AuNPs–GC electrode response to Hg(II) trace amounts was also studied and its optimal value confirmed to be in the 10−2M range. Finally, the AuNPs–GC electrode was used for the determination of Hg(II) in a natural groundwater sample from south of France. By using a preconcentration time of 3000s, a Hg(II) concentration of 19±3pM was found, which compared well with the result obtained by cold vapor atomic fluorescence spectroscopy (22±2pM).

Determination of mercury species by the diffusive gradient in thin film technique and liquid chromatography – atomic fluorescence spectrometry after microwave extraction

A diffusive gradient in thin films technique (DGT) was combined with liquid chromatography (LC) and cold vapor atomic fluorescence spectrometry (CV-AFS) for the simultaneous quantification of four mercury species (Hg2+, CH3Hg+, C2H5Hg+, and C6H5Hg+). After diffusion through an agarose diffusive layer, the mercury species were accumulated in resin gels containing thiol-functionalized ion-exchange resins (Duolite GT73, and Ambersep GT74). A microwave-assisted extraction (MAE) in the presence of 6M HCl and 5M HCl (55°C, 15min) was used for isolation of mercury species from Ambersep and Duolite resin gels, respectively. The extraction efficiency was higher than 95.0% (RSD 3.5%). The mercury species were separated with a mobile phase containing 6.2% methanol+0.05% 2-mercaptoethanol+0.02M ammonium acetate with a stepwise increase of methanol content up to 80% in the 16th min on a Zorbax C18 reverse phase column. The LODs of DGT–MAE–LC–CV-AFS method were 38ngL−1 for CH3Hg+, 13ngL−1 for Hg2+, 34ngL−1 for C2H5Hg+ and 30ngL−1 for C6H5Hg+ for 24h DGT accumulation at 25°C.

Mercury(ii) and methylmercury determination in water by liquid chromatography hyphenated to cold vapour atomic fluorescence spectrometry after online short-column preconcentration

A method developed for the online preconcentration and speciation of mercury in water involves low sample volume and simple sample pre-treatment for obtaining good recoveries regardless of the water matrix composition.

Development of a deep-sea mercury sensor using <i>in situ</i> anodic stripping voltammetry

Copyright © 2015 by The Geochemical Society of Japan. mercury in seawater can be an indicator of widespread underwater mineral deposits (Marumo et al., 2008; Tomiyasu et al., 2007). Therefore, deep-sea mercury monitoring is very important to both the caution of environmental pollution and the exploration of underwater mineral deposits. Due to their high sensitivity, cold vapor atomic absorption spectrometry (CV-AAS) (Chakraborty et al., 2014a, c), cold vapor atomic fluorescence spectrometry (CV-AFS) (Fernandez-Martinez et al., 2015), and inductively coupled plasma mass spectrometry (ICP-MS) (Baya et al., 2015) have been the most commonly used for the measurement of total mercury. All of these techniques require expensive and sophisticated instrumentation combined with complicated sample preparation processes (Chakraborty et al., 2015; Ferreira et al., 2015; Giacomino et al., 2008). Sample collection needs certain spatial and temporal resolutions of the target fields, and there is a risk of contamination and/or loss of mercury during the sampling and transfer of water from depth to the surface Development of a deep-sea mercury sensor using in situ anodic stripping voltammetry

Total Mercury Determination in Petroleum Green Coke and Oily Sludge Samples by Cold Vapor Atomic Fluorescence Spectrometry

A fast, simple and reliable method for Hg determination in green coke and oily sludge samples by atomic fluorescence spectrometry is described. Microwave digestion and extraction procedures were evaluated for highly complex samples of coke and oily sludge. The concentrations of SnCl2 and HCl to promote Hg vapor, were optimized, as well as the concentration of KMnO4, to stabilize the Hg2+ before the atomic vapor formation. Accuracy of the method was evaluated through certified reference material, for green coke, and comparison with cold vapor atomic absorption spectrometry (CV AAS), for oily sludge. Recovery tests were also performed. Limits of detection and quantification were 0.8 and 2.6 µg kg−1, respectively. Ten green coke and nine sludge samples were analysed and Hg concentrations in coke are very low, between 0.005 and 0.065 mg kg−1, but oily sludge samples have high concentrations, ranging from 42.5 to 376.6 mg kg−1, requiring careful management.

Deployment of a sequential two-photon laser-induced fluorescence sensor for the detection of gaseous elemental mercury at ambient levels: fast, specific, ultrasensitive detection with parts-per-quadrillion sensitivity

Abstract. The operation of a laser-based sensor for gas-phase elemental mercury, Hg(0), is described. It utilizes sequential two-photon laser excitation with detection of blue-shifted laser-induced fluorescence (LIF) to provide a highly specific detection scheme that precludes detection of anything other than atomic mercury. It has high sensitivity, fast temporal resolution, and can be deployed for in situ measurements in the open atmosphere with essentially no perturbation of the environment. An ambient sample can also be pulled through a fluorescence cell, allowing for standard addition calibrations of the concentration. No type of preconcentration is required and there appears to be no significant interferences from other atmospheric constituents, including gas-phase oxidized mercury species. As a consequence, it is not necessary to remove oxidized mercury, commonly referred to as reactive gaseous mercury (RGM), from the air sample. The instrument has been deployed as part of an instrument intercomparison and compares well with conventional instrumentation that utilizes preconcentration on gold followed by analysis using cold-vapor atomic fluorescence spectroscopy (CVAFS). Currently, the achievable detection sensitivity is ~ 15 pg m−3 (~ 5 × 104 atoms cm−3, ~ 2 ppq) at a sampling rate of 0.1 Hz, i.e., averaging 100 shots with a 10 Hz laser system. Preliminary results are described for a 50 Hz instrument that utilizes a modified excitation sequence and has monitored ambient elemental mercury with an effective sampling rate of 10 Hz. Additional work is required to produce the precision necessary to perform eddy correlation measurements. Addition of a pyrolysis channel should allow for the measurement of total gaseous mercury (TGM) and hence RGM (by difference) with good sensitivity and time resolution.

Evaluation of different digestion systems for determination of trace mercury in seaweeds by cold vapour atomic fluorescence spectrometry

Four methods for acid digestion of seaweeds were compared in 10 commercially available seaweeds: (i) in stainless steel-Teflon®PTFE-bombs at high pressure and temperature, (ii) in closed-Teflon®PFA-vessels at high pressure and temperature, (iii) in open-polypropylene-tubes with reflux caps in a graphite heating block at high temperature and (iv) in closed-TFM™PTFE-vessels with microwave-assisted controlled pressure and temperature. Hg was determined in all digests by cold vapour atomic fluorescence spectrometry (CV-AFS). Assessment of digestion methods was performed by comparison with the results obtained for total mercury determination by the Method EPA 7473, based on direct mercury analysis in the solid samples, and with a reference material BCR-279. The open vessel digestion system with reflux in a graphite heating block at high temperature constitutes the best choice since it was found to give the better Hg extraction (83–103%) as well as the lowest variability, being RSD<10% for most of the studied seaweeds. A previous freeze-drying and intensive grinding was the best pre-treatment. Similar results were obtained with and without the presence of oxidizing agents (KMnO4, K2Cr2O7) and with different tube-materials (borosilicate glass, PTFE and polypropylene).

Direct online HPLC-CV-AFS method for traces of methylmercury without derivatisation: a matrix-independent method for urine, sediment and biological tissue samples.

Mercury (Hg) is a global pollutant which occurs in different species, with methylmercury (MeHg) being the critical compound due to its neurotoxicity and bioaccumulation through the food chain. Methods for trace speciation of MeHg are therefore needed for a vast range of sample matrices, such as biological tissues, fluids, soils or sediments. We have previously developed an ultra-trace speciation method for methylmercury in water, based on a preconcentration HPLC cold vapour atomic fluorescence spectrometry (HPLC-CV-AFS) method. The focus of this work is mercury speciation in a variety of sample matrices to assess the versatility of the method. Certified reference materials were used where possible, and samples were spiked where reference materials were not available, e.g. human urine. Solid samples were submitted for commonly used digestion or extraction processes to obtain a liquid sample for injection into the analytical system. For MeHg in sediment samples, an extraction procedure was adapted to accommodate MeHg separation from high amounts of Hg(2+) to avoid an overload of the column. The recovery for MeHg determination was found to be in the range of 88-104% in fish reference materials (DOLT-2, DOLT-4, DORM-3), lobster (TORT-2), seaweed (IAEA-140/TM), sediments (ERM(®)-CC580) and spiked urine and has been proven to be robust, reliable, virtually matrix-independent and relatively cost-effective. Applications in the ultra-trace concentration range are possible using the preconcentration up to 200 mL, while for higher MeHg-containing samples, lower volumes can be applied. A comparison was carried out between species-specific isotope dilution gas chromatography inductively coupled plasma mass spectrometry (SSID-GC-ICP-MS) as the gold standard and HPLC-CV-AFS for biological tissues (liver, kidney and muscle of pilot whales), showing a slope of 1.008 and R (2) = 0.97, which indicates that the HPLC-CV-AFS method achieves well-correlated results for MeHg in biological tissues.

Methylmercury in water samples at the pg/L level by online preconcentration liquid chromatography cold vapor-atomic fluorescence spectrometry

Ultra-traces of methylmercury at the sub-ppt level can be magnified in the foodweb and is of concern. In environmental monitoring a routine robust analytical method is needed to determine methylmercury in water. The development of an analytical method for ultra-trace speciation analysis of methylmercury (MeHg) in water samples is described. The approach is based on HPLC-CV-AFS with on-line preconcentration of water samples up to 200mL, resulting in a detection limit of 40pg/L (ppq) for MeHg, expressed as Hg. The unit consists of an optimized preconcentration column filled with a sulfur-based sorption material, on which mercury species are preconcentrated and subsequently eluted, separated and detected via HPLC-CV-AFS (high performance liquid chromatography–cold vapor atomic fluorescence spectrometry). During the method development a type of adsorbate material, the pH dependence, the sample load rate and the carry-over were investigated using breakthrough experiments. The method shows broad pH stability in the range of pH0 to 7, without the need for buffer addition and shows limited matrix effects so that MeHg is quantitatively recovered from sewage, river and seawater directly in the acidified samples without sample preparation.

Mackinawite (FeS) reduces mercury(II) under sulfidic conditions.

Mercury (Hg) is a toxicant of global concern that accumulates in organisms as methyl Hg. The production of methyl Hg by anaerobic bacteria may be limited in anoxic sediments by the sequestration of divalent Hg [Hg(II)] into a solid phase or by the formation of elemental Hg [Hg(0)]. We tested the hypothesis that nanocrystalline mackinawite (tetragonal FeS), which is abundant in sediments where Hg is methylated, both sorbs and reduces Hg(II). Mackinawite suspensions were equilibrated with dissolved Hg(II) in batch reactors. Examination of the solid phase using Hg LIII-edge extended X-ray absorption fine structure (EXAFS) spectroscopy showed that Hg(II) was indeed reduced in FeS suspensions. Measurement of purgeable Hg using cold vapor atomic fluorescence spectrometry (CVAFS) from FeS suspensions and control solutions corroborated the production of Hg(0) that was observed spectroscopically. However, a fraction of the Hg(II) initially added to the suspensions remained in the divalent state, likely in the form of β-HgS-like clusters associated with the FeS surface or as a mixture of β-HgS and surface-associated species. Complexation by dissolved S(-II) in anoxic sediments hinders Hg(0) formation, but, by contrast, Hg(II)–S(-II) species are reduced in the presence of mackinawite, producing Hg(0) after only 1 h of reaction time. The results of our work support the idea that Hg(0) accounts for a significant fraction of the total Hg in wetland and estuarine sediments.

Determination of total mercury in nuts at ultratrace level

Total mercury, at μgkg−1 level, was determined in different types of nuts (cashew nut, Brazil nuts, almond, pistachio, peanut, walnut) using a direct mercury analyser after previous sample defatting and by cold vapour atomic fluorescence spectrometry. There is not enough sensitivity in the second approach to determine Hg in previously digested samples due to the strong matrix effect. Mercury levels in 25 edible nut samples from Brazil and Spain were found in the range from 0.6 to 2.7μgkg−1 by using the pyrolysis of sample after the extraction of the nut fat. The accuracy of the proposed method was confirmed by analysing certified reference materials of Coal Fly Ash-NIST SRM 1633b, Fucus-IAEA 140 and three unpolished Rice Flour NIES-10. The observed results were in good agreement with the certified values. The recoveries of different amounts of mercury added to nut samples ranged from 94 to 101%. RSD values corresponding to three measurements varied between 2.0 and 14% and the limit of detection and quantification of the method were 0.08 and 0.3μgkg−1, respectively.

Method development for the simultaneous determination of methylmercury and inorganic mercury in seafood

This paper reports the method development for the simultaneous determination of methylmercury (MeHg+) and inorganic mercury (iHg) species in seafood samples. The study focused on the extraction and quantification of MeHg+ (the most toxic species) by liquid chromatography coupled to on-line UV irradiation and cold vapour atomic fluorescence spectroscopy (LC-UV-CV-AFS), using HCl 4 mol L−1 as the extractant agent. Accuracy of the method has been verified by analysing three certified reference materials and different spiked samples. The values found for total Hg and MeHg+ for the CRMs did not differ significantly from certified values at a 95% confidence level, and recoveries between 85% and 97% for MeHg+, based on spikes, were achieved. The detection limits (LODs) obtained were 0.001 mg Hg kg−1 for total mercury, 0.0003 mg Hg kg−1 for MeHg+ and 0.0004 mg Hg kg−1 for iHg. The quantification limits (LOQs) established were 0.003 mg Hg kg−1 for total mercury, 0.0010 mg Hg kg−1 for MeHg+ and 0.0012 mg Hg kg−1 for iHg. Precision for each mercury species was established, being ≤ 12% in terms of RSD in all cases. Finally, the developed method was applied to 24 seafood samples from different origins and total mercury contents. The concentrations for Total Hg, MeHg+ and iHg ranged from 0.07 to 2.33, 0.003–2.23 and 0.006–0.085 mg Hg kg−1, respectively. The established analytical method allows to obtain results for mercury speciation in less than 1 one hour including both, sample pretreatment and measuring step.

Cold vapor generation of Zn based on dielectric barrier discharge induced plasma chemical process for the determination of water samples by atomic fluorescence spectrometry.

A new plasma chemical vapor generation (plasma-CVG) method for Zn was developed by dielectric barrier discharge (DBD). The dissolved Zn ions was readily converted to volatile species by DBD plasma in the presence of hydrogen and then, the generated Zn vapor, Zn(0), was detected by cold vapor atomic fluorescence spectrometry (AFS). It eliminated the use of unstable tetrahydroborate-reducing reagent and high-purity acids. The operating conditions for the DBD plasma-CVG system were optimized for the efficient vapor generation of Zn. In addition, possible interferences from coexisting ions on the plasma-CVG of Zn were also examined. No appreciable matrix interference was found from most of the examined ions at concentration of 1 mg L(-1). However, severe depression of the Zn vapor generation efficiency was observed in the presence of ions at 10 mg L(-1). Under the optimal conditions, the limit of detection (LOD) was calculated to be 0.2 μg L(-1); good repeatability (relative standard deviation (RSD) = 2.6%, n = 11) was obtained for a 20 Zn μg L(-1) standard. The accuracy of the proposed method was validated though analysis of Zn in reference material of simulated natural water sample GSB07-1184-2000 and the determined result was in good agreement with the reference value. The proposed method has also been successfully applied to the determination of Zn in Changjiang River water, Wuhan East Lake water, and Wuhan tap water samples. It provides an alternative green vapor generation method for Zn.

Environmental neurotoxins β-N-methylamino-l-alanine (BMAA) and mercury in shark cartilage dietary supplements

Shark cartilage products are marketed as dietary supplements with claimed health benefits for animal and human use. Shark fin and cartilage products sold as extracts, dry powders and in capsules are marketed based on traditional Chinese medicine claims that it nourishes the blood, enhances appetite, and energizes multiple internal organs. Shark cartilage contains a mixture of chondroitin and glucosamine, a popular nutritional supplement ingested to improve cartilage function. Sharks are long-lived apex predators, that bioaccumulate environmental marine toxins and methylmercury from dietary exposures. We recently reported detection of the cyanobacterial toxin β-N-methylamino-l-alanine (BMAA) in the fins of seven different species of sharks from South Florida coastal waters. Since BMAA has been linked to degenerative brain diseases, the consumption of shark products may pose a human risk for BMAA exposures. In this report, we tested sixteen commercial shark cartilage supplements for BMAA by high performance liquid chromatography (HPLC-FD) with fluorescence detection and ultra performance liquid chromatography/mass spectrometry/mass spectrometry (UPLC–MS/MS). Total mercury (Hg) levels were measured in the same shark cartilage products by cold vapor atomic fluorescence spectrometry (CVAFS). We report here that BMAA was detected in fifteen out of sixteen products with concentrations ranging from 86 to 265μg/g (dry weight). All of the shark fin products contained low concentrations of Hg. While Hg contamination is a known risk, the results of the present study demonstrate that shark cartilage products also may contain the neurotoxin BMAA. Although the neurotoxic potential of dietary exposure to BMAA is currently unknown, the results demonstrate that shark cartilage products may contain two environmental neurotoxins that have synergistic toxicities.