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Marine toxins pose a significant safety risk, leading to human intoxications and causing substantial economic losses in seafood-producing regions. The development of rapid, cost-effective, efficient, and reliable approaches for the containment of these substances is therefore crucial in order to mitigate the adverse impact of marine toxins. This research conducted a comprehensive review on the toxicity and influencing factors of marine toxins production. Additionally, depuration technologies, including adsorption, advanced oxidation processes, biodegradation, heating treatment, temporary maintenance and purification, and drug inhibition, were systematically summarized. The study also provided a comparative analysis of the advantages and disadvantages of various depuration technologies and proposed strategies for future development. [Display omitted] • The toxicity, distribution and influencing factors of marine toxins were examined. • Depuration technologies, like AOPs, biodegradation, adsorption have been updated. • The cutting-edge materials and techniques were extensively discussed. • The advantages and disadvantages of different depuration methods were compared. [ABSTRACT FROM AUTHOR]

Norovirus is a significant global cause of viral gastroenteritis, with raw oyster consumption often linked to such outbreaks due to their filter-feeding in harvest waters. National water quality and depuration/relaying times are often classified using Escherichia coli , a poor proxy for norovirus levels in shellfish. The current norovirus assay is limited to only the digestive tracts of oysters, meaning the total norovirus load of an oyster may differ from reported results. These limitations motivated this work, building upon previous modelling by the authors, and considers the sequestration of norovirus into observed and cryptic (unobservable) compartments within each oyster. Results show that total norovirus levels in shellfish batches exhibit distinct peaks during the early depuration stages, with each peak's magnitude dependent on the proportion of cryptic norovirus. These results are supported by depuration trial data and other studies, where viral levels often exhibit multiphase decays. This work's significant result is that any future norovirus legislation needs to consider not only the harvest site's water classification but also the total viral load present in oysters entering the market. We show that 62 h of depuration should be undertaken before any norovirus testing is conducted on oyster samples, being the time required for cryptic viral loads to have transited into the digestive tracts where they can be detected by current assay, or have exited the oyster. • Several studies report multiphase decay of norovirus in oysters during depuration. • The model splits norovirus loads into cryptic (unobservable) and observable compartments within oysters. • Results synthesise reported multiphase decay of norovirus, with levels of cryptic norovirus dissipating after ≈ 62 hours of depuration. • To minimise food safety risks to consumers, any future legislation should assay oyster norovirus levels after 62 h of depuration to account for any cryptic norovirus levels present. [ABSTRACT FROM AUTHOR]

Abstract This study investigated the influences of seawater to oyster ratio on depuration for decontaminating V. parahaemolyticus in raw oysters with a goal of identifying the proper ratio of oyster to seawater capable of improving the efficacy of the depuration process. The water to oyster ratios tested in this study ranged from 1.0 to 2.5 L of artificial seawater (ASW) per oyster (40 oysters in 40, 60, 80 and 100 L ASW). The depuration efficacy for purging V. parahaemolyticus from oysters was highest when we applied a 2:1, followed by 1.5:1, 2.5:1, and 1:1 L of ASW/oyster. Further studies of depuration with 2:1 L of ASW/oyster found that the concentration of V. parahaemolyticus in oysters decreased in a nonlinear manner. The depuration curve was fitted to a one phase decay model with a coefficient of determination (R2) of 0.933. The time for a 3 log reduction was 1.75 days with a 95% confidence interval from 1.65 to 1.85 days, which meets the FDA's requirement of larger than a 3.0 log (MPN/g) reduction as a post-harvest process for V. parahaemolyticus control. After 4 days levels in all trials were <100 MPN/g meeting performance standards established by Japan and Canada. Furthermore, the time for a 3.52 log reduction was 3.17 days with a 95% confidence interval from 2.92 to 3.54 days but it took 5 days to reduce levels to <30 MPN/g, which satisfies FDA's requirement as a post-harvest control process (>3.52 log MPN/g reduction) for the purpose of making safety added labeling claims for V. parahaemolyticus. Highlights • V. parahaemolyticus purge rates depended on oyster stocking density and water temperature. • Optimal purging V. parahaemolyticus (>3.00 log) occurred with 1 oyster/2 liter of seawater at 12.5°C in 2 days. • V. parahaemolyticus levels in oysters were reduced to <100 MPN/g within 4 days and <30MPN/g after 5 days. • NSSP V. parahaemolyticus reduction targets and international mandated levels were achieved. [ABSTRACT FROM AUTHOR]

Abstract Seashore invertebrates such as mussels are exposed to multiple bouts of pollution related to human activities. Plastic debris originating from land-based activities are a concerning issue as they may be fragmented in smaller pieces (microplastics, < 5 mm diameter) which have an excellent potential for uptake by a large variety of animals. Here, we set out to explore the whole transcriptome profiling of Mytilus galloprovincialis associated with temporal variability of microplastics concentrations. Mussels were submitted to (i) a single 18 days-exposure to a concentration of microplastics found during pollution events (4.6 E+5 polyethylene microbeads L−1), (ii) a recovery period to investigate the reversibility of microplastics effects and (iii) a repeated exposure to microplastics to evidence acclimation to microplastics pollution events. Overall, 18 days-exposure to microplastics was mostly associated with disruption of mussel global homeostasis resulting in the production of stress and immune-related proteins and as a consequence, a diminution of energy allocated to growth. During the recovery period, a contrasting response was observed with the activation of apoptotic processes and the up-regulation of immune-receptors and stress-related proteins (glutathione peroxidase , hsp70) in mussels previously exposed to microplastics. These divergent responses, suggest that the establishment of compensatory mechanism as an attempt to recover, is not sufficient to counteract physiological stress induced by the first exposure. Finally, the differences observed in gene expression between single and repeated exposures to microplastics suggest, under the experimental conditions tested, that mussels may be able to establish a stress-memory upon microplastics exposure. Highlights • High concentrations of microplastics (MP) had disruptive effects on mussels' homeostasis. • Stress and physical damages provoked by MPs persisted after a single exposure event. • Distinct transcriptomic patterns were observed after single and a repeated exposure to microplastics. [ABSTRACT FROM AUTHOR]

Lead (Pb) is a non-essential metal. Its occurrence in the environment is related principally to anthropogenic contamination. Pb is toxic to aquatic organisms and can provoke damage to membranes and inhibit the activity of essential enzymes. The filter-feeding, Manila clam Ruditapes philippinarum is widely used as a biomonitor organism to assess metal toxicity. Among biomarkers related to the Pb toxicity, the enzymatic activity of δ-aminolevulinic acid dehydratase (δ-ALAD) has been adopted as a specific tool. Metallothionein (MT), lipid peroxidation (LPO) and antioxidant enzymes activities, such as catalase (CAT), glutathione peroxidase (GPx), glutathione reductase (GR) and glutathione S-transferase (GST) and superoxidase dismutase (SOD) have also been employed to assess the toxic effect of metals. Two target tissues, the gills and the digestive gland, were selected to examine biomarker responses. In order to assess the effects of Pb accumulation and the mechanisms involved in the recovery from it, clams were exposed at two Pb levels (10 and 100 µg/L) for 7 days and were later maintained in clean water for 7 days as a depuration period. Pb accumulation was dependent on the exposure concentration and higher Pb levels were observed in the gills compared to the digestive gland. Inhibition of δ-ALAD, GST and SOD and the induction of MT and LPO over the exposure period were observed in the gills and the digestive gland of R. philippinarum . The depuration period showed a continuous inhibition of the δ-ALAD activity and induction of MT and LPO in both tissues. These results demonstrate that lead induced an exposure effect and the 7 days of depuration were not sufficient to recover the basal health status of the clams. [ABSTRACT FROM AUTHOR]

We previously demonstrated that chronic exposure to hexavalent chromium (Cr(VI)) causes a variety of adverse effects in the Japanese medaka ( Oryzias latipes ). The present study investigated the transition of acute to chronic effects by assessing the influences of Cr(VI) exposure concentration and exposure duration on Cr accumulation and their effects on fish growth and antioxidant physiology. Juvenile fish were exposed to 0.05, 0.5, 4 or 8 mg/L Cr(VI) for 28 days. Endpoints were evaluated on days 3, 7, 14, 21 and 28. In addition, Cr depuration was examined for fish from two exposure groups (0.5 and 8 mg/L). Chromium accumulation was rapid initially, then continued at a slower rate till the end of the exposure period without showing signs of reaching a steady state. Depuration patterns differed between the two exposure groups, but both reached 50% in 14 days. The rapid initial accumulation was accompanied by increased lipid peroxidation and elevated activities of antioxidants (e.g., GST, SOD and CAT). Activities of these enzymes had mostly returned to baseline levels by day 7, but there was no evidence of further cellular damage from ROS. Effects on fish length and weight continued to be evident over the 28-day exposure period. Our study suggest that the initial effects of Cr(VI) exposure may not be a good predictor of more-chronic effects in fish as a consequence of an efficient acclimation response by the antioxidant system that limits ROS-mediated toxicity. [ABSTRACT FROM AUTHOR]

Depuration is a vital stage to ensure the safety of oyster consumption, and salinity had a great impact on the environmental adaptability of oysters, but the underlying molecular mechanism was poorly understood during depuration stage. Here, Crassostrea gigas was depurated for 72 h at different salinity (26, 29, 32, 35, 38 g/L, corresponding to ±20%, ±10% salinity fluctuation away from oyster's production area) and then analyzed by using transcriptome, proteome, and metabolome combined with bioinformatics techniques. The transcriptome showed that the salinity stress led to 3185 differentially expressed genes and mainly enriched in amino acid metabolism, carbohydrate metabolism, lipid metabolism, etc. A total of 464 differentially expressed proteins were screened by the proteome, and the number of up-regulated expression proteins was less than the down-regulated, indicating that the salinity stress would affect the regulation of metabolism and immunity in oysters. 248 metabolites significantly changed in response to depuration salinity stress in oysters, including phosphate organic acids and their derivatives, lipids, etc. The results of integrated omics analysis indicated that the depuration salinity stress induced abnormal metabolism of the citrate cycle (TCA cycle), lipid metabolism, glycolysis, nucleotide metabolism, ribosome, ATP-binding cassette (ABC) transport pathway, etc. By contrast with Pro-depuration, more radical responses were observed in the S38 group. Based on the results, we suggested that the 10% salinity fluctuation was suitable for oyster depuration and the combination of multi-omics analysis could provide a new perspective for the analysis of the mechanism changes. • Multi-omics was applied to study depuration salinity effect on C. gigas. • 248 metabolites, 464 proteins, and 3185 genes were significantly altered. • More radical responses were observed in the S38 group. • 10% salinity fluctuation was suitable for oyster depuration. [ABSTRACT FROM AUTHOR]

Data from the 2001–2004 National Health and Nutrition Examination Survey (NHANES) were used to evaluate serum concentrations of polychlorinated biphenyls (PCBs) in women of reproductive age, with or without a history of breastfeeding. Analytical data for PCBs 138, 153, and 180 were used along with responses to the NHANES Reproductive Health questions: [Have you] breastfed any of your children? ” and “[What] number of children [have been] breastfed [for] at least 1 month? ” PCB concentrations were found to be significantly lower among 15–44 year old women who had a history of breastfeeding compared to those who had not breastfed any of their children. Based on data for 474 women, ages 15–44 years, mean serum PCB 138, 153, and 180 concentrations were 16.4, 21.4, and 14.3 ng/g lipid for women who have a history of breastfeeding, and 24.0, 30.0, and 21.4 ng/g lipid for women who have not breastfed, respectively. These results were weighted using the 2001–2004 sample weights provided by NHANES to represent over 27 million U.S. women. PCB concentrations were also lower among women who had breastfed multiple children. Mean serum PCB 138, 153, and 180 concentrations were 11.8, 15.2, and 10.1 ng/g lipid, respectively, for women 35–44 years who had breastfed six children and 22.7, 31.9, and 22.5 ng/g lipid, respectively, for women 35–44 years who had breastfed only one child. The results tend to support the long-standing hypothesis that depuration of PCBs may occur via breastfeeding. [ABSTRACT FROM AUTHOR]

We investigated the effect of depuration of three naturally contaminated commercially important tropical edible bivalve molluscs by varying temperature, salinity and body-size of animals harvested from Ashtamudi and Vembanad estuaries, India using a static depuration system to ensure microbiological food safety. Before depuration, the levels of faecal indicators and pathogens were above the acceptable limits for live consumption. The depuration water temperature had a significant effect on bacterial elimination. Log reduction of faecal coliforms (FC) and E. coli varied between room-temperature (RTDS) and low-temperature depuration system (LTDS) and it was in the range of 1.39–2.44 and 1.88–2.82 log MPN, respectively under RTDS and LTDS. The elimination of bacterial pathogens such as Vibrio and Salmonella spp. was rapid in RTDS compared to LTDS. The highest elimination of FC and E. coli (2.39 and 2.92 log) was at 35 psμ depuration and the lowest (0.87 and 1.65 log) at 15 psμ depuration. The reduction of FC and E. coli was higher in the medium-sized animals compared to the small animals. Based on the results it is recommended that depuration using the static system under room-temperature (30 ± 1 °C); a salinity range of (25–35 psμ) and using medium-size bivalves (clam>30 mm; mussel >45 mm, and oyster >65 mm length) as optimum conditions for producing microbiologically safe bivalves for live consumption within 36 h. • Process protocols for the depuration of tropical clams, mussels and oysters were advanced. • High levels of FIBs and human pathogenic contamination were found and eliminated. • Room-temperature depuration eliminated Vibrio spp. and Salmonella spp. rapidly. • Depuration at high salinity favours the elimination of indicator bacteria and pathogens. • The size of the bivalve played a critical role in depuration efficiency. [ABSTRACT FROM AUTHOR]

Bisphenol AF (BPAF) is an analog of Bisphenol A (BPA) and is widely used as a raw material in the plastics industry. However, an understanding of the potential risks posed by BPAF in the aquatic environment is lacking. The bioconcentration factor (BCF) is a measure used to assess the secondary poisoning potential as well as risks to human health. In this work we measured the accumulation and elimination of BPAF in the whole-body and in liver, muscle and gonad tissues of zebrafish. BPAF uptake was relatively rapid with equilibrium concentrations reached after 24–72 h of exposure. We observed gender differences both in whole-body and in tissue accumulation. Muscle was the primary BPAF storage tissue during the uptake phase in this study. In the elimination phase, BPAF concentrations declined rapidly during depuration, especially during the initial 2 h, and the rate of elimination in males was faster than females from the whole-body and from tissues. The appearance of BPAF glucuronide (BPAF-G) at the start of the uptake phase indicated the rapid biotransformation of BPAF to BPAF-G in vivo. The high lipid content of female gonad could act to delay the diffusion of the xenobiotic within the body in a contaminated environment, but it also acts to delay xenobiotic elimination from the body. [ABSTRACT FROM AUTHOR]

Molluscan shellfish can cause food borne diseases and here we investigated if addition of Vibrio -antagonising bacteria could reduce Vibrio vulnificus in model oyster systems and prevent its establishment in live animals. Phaeobacter inhibens , which produces an antibacterial compound, tropodithietic acid (TDA), inhibited V. vulnificus as did pure TDA (MIC of 1–3.9 μM). P. inhibens DSM 17395 (at 10 6 cfu/ml) eradicated 10 5 cfu/ml V. vulnificus CMCP6 (a rifampicin resistant variant) from a co-culture oyster model system (oyster juice) whereas the pathogen grew to 10 7 cfu/ml when co-cultured with a TDA negative Phaeobacter mutant. P. inhibens grew well in oyster juice to 10 8 CFU/ml and sterile filtered samples from these cultures were inhibitory to Vibrio spp. P. inhibens established itself in live European flat oysters ( Ostrea edulis ) and remained at 10 5 cfu/g for five days. However, the presence of P. inhibens could not prevent subsequently added V. vulnificus from entering the live animals, likely because of too low levels of the biocontrol strain. Whilst the oyster model studies provided indication that P. inhibens DSM 17395 could be a good candidate as biocontrol agent against V. vulnificus further optimization is need in the actual animal rearing situation. [ABSTRACT FROM AUTHOR]

The objective of the present study was to investigate the uptake, depuration, and bioconcentration of two pharmaceuticals, roxithromycin (ROX) and propranolol (PRP), in Daphnia magna via aqueous exposure. Additionally, dietary and pH effects on the bioconcentration of two pharmaceuticals in daphnia were studied. During the 24-h uptake phase followed by the 24-h depuration phase, the uptake rate constants ( k u ) of ROX for daphnia were 9.21 and 2.77 L kg − 1 h −1 , corresponding to the exposure concentrations of 5 and 100 μg L −1 , respectively; For PRP at the nominal concentrations of 5 and 100 μg L −1 , k u were 2.29 and 0.99 L kg −1 h −1 , respectively. The depuration rate constants ( k d ) of ROX in daphnia, at the exposure concentrations of 5 and 100 μg L −1 , were 0.0985 and 0.207 h −1 , respectively; while those of PRP were 0.0276 and 0.0539 h −1 for the nominal concentrations of 5 and 100 μg L −1 , respectively. With the decreasing exposure concentrations, the bioconcentration factors (BCFs) in daphnia ranged from 13.4 to 93.5 L kg −1 for ROX, and 18.4 to 83.0 L kg −1 for PRP, revealing the considerable accumulation potential of these two pharmaceuticals. Moreover, after 6 h exposure, the body burdens of ROX and PRP in dead daphnia were 4.98–6.14 and 7.42–12.9 times higher than those in living daphnia, respectively, implying that body surface sorption dominates the bioconcentration of the two pharmaceuticals in daphnia. In addition, the presence of algal food in the media could significantly elevate the k d values for both ROX and PRP, thereby restraining their bioconcentration in daphnia. A pH-dependent bioconcentration study revealed that the bioconcentration of the two pharmaceuticals in daphnia increased with increasing pH levels, which ranged from 7 to 9. Finally, a model was developed to estimate the relationships between pH and the BCFs of the two pharmaceuticals in zooplankton. The predicted values based on this model were highly consistent with wildlife monitoring data, implying that this model will be useful in identifying the bioaccumulation risks that pharmaceuticals pose to zooplankton. [ABSTRACT FROM AUTHOR]

This study aimed to determine the accumulation and maternal transfer of perfluorooctane sulphonic acid (PFOS) in yellow-legged gulls (YLG, Larus michahellis ) and the protected species Audouin's gull (AG, Larus audouinii ), which cohabit in the Ebro Delta Natural Park (Catalonia, Spain). The Estimated Daily Intake (EDI) through diet (fish and crayfish), depuration rates and transfer capacity from blood to first eggs was studied for a set of 44 pairs. For AG, mean (±SD) EDI was of 128±36 ng/d in males and 119±32 ng/d in females, and for YLG, 170±48 ng/d in males and 159±42 ng/d in females. PFOS levels in blood were higher in males than females (60.6±21 and 61.1±27 ng/g ww in AG and YLG males versus 25.2±12 and 27.3±14 ng/g ww in AG and YLG females), with little differences among species. The lower levels in females were attributed to the annual release of PFOS to eggs during the laying period, which was estimated of 5544±1571 ng/egg for AG females and 6716±2689 ng/egg for YLG. The overall mass balance of PFOS calculated for both species clearly demonstrates that uptake is higher than elimination rates, considering depuration rates and transfer of PFOS to eggs, and this explains that PFOS is accumulated in gulls in a yearly basis. [ABSTRACT FROM AUTHOR]

Abstract: The efficacy and dynamic of depuration for the removal of hepatitis A virus (HAV) contamination were evaluated under experimental conditions using Manila clams previously subjected to bioaccumulation with this virus. Five independent trials were assayed in a closed experimental system with a total volume of approximately 1750 l, using clam batches of 60 Kg. The reverse transcriptase-real time PCR (RT-qPCR) technique was utilized for viral quantification. Infectivity assays were conducted at the end of depuration. Although the final viral loads in shellfish after 7 days remained relatively high and still infectious, an average reduction in HAV levels of 1.44 log units (approx. 93.1%) was observed. This reduction showed a two-phase removal kinetic, with an initial rapid reduction of viruses during the first 72 h of depuration, with a 0.6 log units (69%) of average decrease in HAV RNA copies/g digestive tissue, and a subsequent stabilization with a slower depuration rate in the remaining days. [Copyright &y& Elsevier]

Abstract: During the warmer summer months, oysters are conditioned to spawn, resulting in massive physiological efforts for gamete production. Moreover, the higher temperatures during the summer typically result in increased bacteria populations in oysters. We hypothesized that these animals are under multiple stresses that lead to possible immune system impairments during the summer months that can possibly lead to death. Here we show that in the summer and the fall animals exposed to a short heat stress respond similarly, resulting in a general trend of more bacteria being found in heat shocked animals than their non-heat shocked counterparts. We also show that naturally occurring bacterial populations are effected by a heat shock. In addition, oysters artificially contaminated with Vibrio parahaemolyticus were also affected by a heat shock. Heat shocked animals contained higher concentrations of V. parahaemolyticus in their tissues and hemolymph than control animals and this was consistent for animals examined during summer and fall. Finally, oyster hemocyte interactions with V. parahaemolyticus differed based on the time of the year. Overall, these findings demonstrate that seasonal changes and/or a short heat shock is sufficient to impact bacterial retention, particularly V. parahaemolyticus, in oysters and this line of research might lead to important considerations for animal harvesting procedures. [Copyright &y& Elsevier]

A medium-term mesocosm exposure study was conducted to elucidate bioaccumulation and depuration of polychlorinated biphenyl congener 153 (PCB-153) in edible shrimp Palaemonetes varians. Over the 15-day exposure period, shrimp under different exposure concentrations exhibited a significant increase in PCB-153 concentration compared with control organisms. Distinct bioaccumulation patterns and uptake rates were observed depending on the exposure concentrations. For low PCB-153 exposure levels (0.25μgL−1), accumulation followed a saturation model, reaching an apparent steady state after fifteen days exposure. For intermediate (2.5μgL−1) and high PCB-153 levels (25μgL−1), accumulation was faster and linear. In addition, the bioaccumulation rate was not proportional to PCB-153 concentration, and the bioaccumulation was higher at intermediate exposure concentrations. Regarding the depuration phase, P. varians lost up to 30% of PCB-153 after 72h and levels continued slowly to decrease until the end of the 30-d experimental period. However, PCB-153 levels in shrimp did not reach background values, and those exposed to moderate and high PCB-153 concentrations presented contamination levels much higher than the regulatory limit for human food consumption (75ngg−1 ww for Σ 6 PCB). [Copyright &y& Elsevier]

The microbiological responses of two bivalves species from Tagus estuary, Venerupis pullastra (native clam) and Ruditapes philippinarum (exotic clam) were investigated during 48 h of depuration and subsequent simulated transport in semi-dry conditions at two temperatures (4 and 22 °C) until reaching 50% lethal time (LT50). Regardless of temperature and species, the maintenance of clams in water for 48 h (depuration period) did not affect LT50 during transport. R. philippinarum showed higher survival rates than V. pullastra, always reaching LT50 later, especially at 4 °C. Significant differences between clams' species were found in almost all microbiological parameters. This can be related with clams' biological activity and habitat environmental conditions since both clams do not coexist in Tagus estuary. Depuration was efficient to reduce the bacterial load, particularly Escherichia coli, but not efficient to remove Vibrio spp. In both species, the growth of Vibrio spp. was inhibited at 4 °C, whereas exponential growth occurred at 22 °C. Total viable counts significantly increased in most treatments, while E. coli counts significantly decreased to undetected levels, except for non-depurated R. philippinarum simulated transported at 4 °C. Thus, this study highlights the importance of clams depuration for at least 24 h in polluted estuarine areas, followed by transport at low temperatures (4 °C). [ABSTRACT FROM AUTHOR]

Abstract: Methylmercury (MeHg) is transferred by female birds into their eggs thus leaving developing embryos exposed to MeHg from the time of fertilization through hatching. Although Hg is a developmental toxicant, little is known about how it distributes among embryonic tissues and subsequently affects neurodevelopment in birds. The main objective of the present study (Part 1 of 2) was to evaluate the distribution of Hg in tissues during different developmental stages in order to better understand potential targets of Hg in the embryo and hatchling. Eight independent, yet related, egg injection studies were conducted. In five studies, white leghorn chicken embryos were air cell injected with methylmercury chloride (MeHgCl; range injected: 0.17–6.4μg/g egg) and Hg concentrations were assessed in seven tissues. We found that soft tissue distribution in embryos and hatchlings was similar to that seen in older birds, with higher total Hg concentrations in liver and kidney than in heart, muscle, and brain (e.g., 5.1, 3.8, 1.9, 2.3, and 1.9μg/g wet weight, respectively, in day 19 embryos after injection with 6.4μg/g MeHgCl). Concentrations were highest in feathers and unabsorbed yolk (e.g., 24.1 and 13.0μg/g in day 19 embryos after injection with 6.4μg/g MeHgCl). Tissue concentrations rose through embryonic days 11, 14, 16, and 19 but generally leveled off at days 1 and 7 post-hatch. We also report on pilot studies that demonstrated that tissue Hg accumulation after MeHgCl injection is similar in chicken and Japanese quail embryos, and that tissue Hg accumulation in chicken embryos after methylmercury cysteine, but not mercury (2) chloride, injection is similar to accumulation after MeHgCl injection. These findings suggest that embryos may accumulate kidney and brain Hg concentrations known to cause renal and neurotoxicity seen in older birds, but that sequestration of Hg into liver and excretion into rapidly growing feathers may offer some protection. This work also demonstrates that air cell injection studies are potentially a useful tool for studies of Hg toxicity in the laboratory. [Copyright &y& Elsevier]

Abstract: Depuration under different salinities was used to reduce the human pathogen Vibrio vulnificus from Eastern oysters (Crassostrea virginica). Individual recirculating systems were used to test the efficacy of depuration at three salinities (15, 25, and 35 psu) in four independent trials during a 14 day period. Initial loads of V. vulnificus were higher than 10,000 MPN/g of oyster meat in all trials. Data showed that 25 and 35 psu treatments were more efficient in reducing V. vulnificus numbers than 15 psu with an overall reduction of >3 logs. A significant decrease in MPN/g was observed as early as day 6 and further reductions were observed at day 10, while longer depurations did not improve efficacy. Only the highest salinity (35 psu) was capable of reducing V. vulnificus numbers to the FDA recommended level of <30 MPN/g in two of the four trials. Oysters survived well in the depuration systems with minimal mortality (<1%) but their condition index (meat quality and yield) decreased during the 14 day period in all treatments. The data presented in this study suggests that high salinity depuration is a promising method to reduce V. vulnificus in oysters. [Copyright &y& Elsevier]

Abstract: Organisms living in coastal ecosystems are frequently subjected to anthropogenic pressures such as metals. Metals, especially those not required for metabolic activity (e.g. mercury, lead and cadmium) can be toxic even at quite low concentrations not only to organisms that accumulate them, but also to their consumers. Throughout the world, Ruditapes decussatus and Ruditapes philippinarum have been successfully commercialised for human consumption and for monitoring environmental conditions such as contamination. These two clam species share similar habitats and requirements, successfully competing both in the natural environment and in aquaculture farms. Because differences in metal accumulation may exist between R. decussatus and R. philippinarum, different risks to public health may overcome as well as distinct ecological implications. The effect of depuration on the metal burden and biochemical status of both clams species may also diverge and since the information available is subjective and scarce, the aims of the present study were to: 1) assess the total metal accumulation and intracellular partitioning, at natural conditions, in the two clam species collected at the same site; 2) evaluate the effect of depuration as a mean of reducing the levels of distinct elements, assessing also the effect of depuration time (2 and 7 days); 3) investigate the efficiency of depuration by biochemical status of the two bivalve species, evaluating changes in lipid peroxidation and activity of antioxidant enzymes catalase (CAT), superoxide dismutase (SOD) and of glutathione S-transferase (GST). Metal chelation by metallothioneins (MTs) was also determined. The results obtained showed that concentration of elements in clams was low, presenting very similar concentration levels for all elements. The present work further demonstrated that the total element concentration decreased in the shorter depuration period (2 days) and that R. decussatus and R. philippinarum partitioned elements preferentially in the insoluble fraction. The percentage of elements in the soluble fraction was lower in the longer depuration period, reducing the dietary bioavailability of elements and thus the health risk to consumers of depurated bivalves. In general, LPO, CAT, SOD and GSTs showed a decreased from environmental to depuration conditions, revealing that depuration reduces the oxidative stress that organisms were subjected in the environment. The lower MTs production observed in the longer depuration period, although no significantly different from the remaining periods, may be explained by the distinct metal allocation between both soluble and insoluble fractions. [Copyright &y& Elsevier]

Abstract: Consumption of raw oysters has been linked to several outbreaks of Vibrio parahaemolyticus infection in the United States. This study investigated effects of ice storage and UV-sterilized seawater depuration at various temperatures on reducing V. parahaemolyticus in oysters. Raw Pacific oysters (Crassostrea gigas) were inoculated with a mixed culture of five clinical strains of V. parahaemolyticus (10290, 10292, 10293, BE 98-2029 and 027-1c1) at levels of 104−6 MPN/g. Inoculated oysters were either stored in ice or depurated in recirculating artificial seawater at 2, 3, 7, 10, 12.5, and 15 °C for 4–6 days. Holding oysters in ice or depuration of oysters in recirculating seawater at 2 or 3 °C for 4 days did not result in significant reductions (P > 0.05) of V. parahaemolyticus in the oysters. However, depuration at temperatures between 7 and 15 °C reduced V. parahaemolyticus populations in oysters by >3.0 log MPN/g after 5 days with no loss of oysters. Depuration at refrigerated temperatures (7–15 °C) can be applied as a post-harvest treatment for reducing V. parahaemolyticus in Pacific oysters. [Copyright &y& Elsevier]

Bioassays measuring the induction of vitellogenin gene expression in male fish are widely used for revealing estrogenic activity in water samples. Measuring induction of vitellogenin mRNA in males by means of RT-PCR analysis is a sensitive way to detect exposure to estrogenic chemicals. To date, little work has been done to examine variations in exposure conditions for assessing estrogenic activity in water samples using this model system. Here we report the results of experiments investigating the effects of volume of treatment water, time since removal from treatment water (depuration), and short-term food deprivation on vitellogenin mRNA induction in male Japanese medaka (Oryzias latipes). Fish exposed to a single concentration of E2 while volume was manipulated were found to have similar levels of vitellogenin mRNA, though more E2 was present at larger volumes. Removal of fish from E2-treated-water to clean water after exposures reduced vitellogenin levels in as little 24h, however, the vitellogenin levels of the fish transferred to the clean water remained above those of the control fish for at least 72h. Depriving fish of food for up to 72h during exposure to E2 did not significantly reduce vitellogenin induction. Together these results support the conclusion that real time RT-PCR measurement of vitellogenin in male fish can be used as a robust indicator of exposure to estrogenic contaminants in water. [Copyright &y& Elsevier]

Abstract: Previous studies demonstrated that microcystins (MCYSTs) can be accumulated in different organs, particularly the liver, of tilapia fish (Oreochromis niloticus) in an Egyptian fish farm containing toxic blooms of Microcystis aeruginosa. In the present study, a microcosm experiment was conducted to examine the depuration of MCYSTs in tilapia fish from this fish farm. Fish were grown in a 100-L aerated recirculation tank containing dechlorinated water at room temperature (25±2°C) for 96h. MCYST concentrations in livers, intestines, and gallbladders of each daily sacrificed fish were determined by both enzyme-linked immunosorbent assay (ELISA) and protein phosphatase inhibition assay (PPIA). MCYST concentrations in the surrounding water were also determined by the same methods. The results showed that MCYST concentrations in the liver and intestine decreased gradually throughout the experimental period. This decrease was accompanied by an increase in MCYST concentrations in the gallbladder and surrounding water. The maximum value of MCYST in the surrounding water was obtained after 96h at a level of 1.2μg/L by ELISA, while it was obtained after 24h at a level of 0.5μg/L by PPIA and remained stable until the end of the experiment. The present study revealed that tilapia fish can depurate and excrete MCYSTs into the bile and surrounding water as a way to avoid toxicity from such a potent hepatotoxin. [Copyright &y& Elsevier]

Neonicotinoids pesticides were introduced to the market in the 1990s to control various pests. Its accumulation in the environment supposes a severe problem that can affect human health. This study investigates the electrochemical degradation of four common neonicotinoid pesticides; thiamethoxam (TMX), imidacloprid (ICP), acetamiprid (ACP) and thiacloprid (TCP), in different natural surface waters by a boron-doped diamond anode (BDD). The most influencing variable was the current density (j), and to a lesser extent, the supporting electrolyte concentration (C e). In optimal conditions (j = 34.14 mA cm−2 and C e = 10.00 mM, using Na 2 SO 4 as electrolyte) pesticide removals for TMX, ICP, ACP and TCP were 97.2, 96.9, 87.8 and 98.2 %, respectively. The obtained results with different support electrolytes (Na 2 SO 4 , NaCl, NaNO 3 and HK 2 PO 4) suggest that sulphate electrolyte was the optimum for TMX, ICP and ACP. However, for TCP, a total removal was achieved in less than 10 min using NaCl. It was also verified that the initial pH of the solution did not significantly influence the process in the range 3–9. All these results were rationalized in this paper. Finally, to evaluate the matrix influence, some experiments were carried out in different natural surface water matrices (river, reservoir and two different WWTP effluents). The factors influencing the process were the conductivity of the solution and the organic matter content. It was noticeable that the specific energy consumption (SEC) reduced by approximately 15 % for river water and WWTP effluent. High mineralization rates were obtained for all water matrices, with TOC removals ranging between 60 and 80 %. [Display omitted] • BDD electrochemical oxidation of neonicotinoid pesticides in natural surface waters: river, reservoir and WWTP effluents. • The most influencing operating variable was the current density and, to a lesser extent, support electrolyte concentration. • The most influential environmental factors in natural surface waters matrices were conductivity and organic matter content. • Specific energy consumption was reduced by approximately 15 % for river water and WWTP effluents compared to ultrapure water. [ABSTRACT FROM AUTHOR]

It is generally expected that biotransformation and excretion of pharmaceuticals occurs similarly in fish and mammals, despite significant physiological differences. Here, we exposed European perch (Perca fluviatilis) to the benzodiazepine drug temazepam at a nominal concentration of 2 µg L−1 for 10 days. We collected samples of blood plasma, muscle, and brain in a time-dependent manner to assess its bioconcentration, biotransformation, and elimination over another 10 days of depuration in clean water. We observed rapid pharmacokinetics of temazepam during both the exposure and depuration periods. The steady state was reached within 24 h of exposure in most individuals, as was complete elimination of temazepam from tissues during depuration. Further, the biologically active metabolite oxazepam was produced via fish biotransformation, and accumulated significantly throughout the exposure period. In contrast to human patients, where a negligible amount of oxazepam is created by temazepam biotransformation, we observed a continuous increase of oxazepam concentrations in all fish tissues throughout exposure. Indeed, oxazepam accumulated more than its parent compound, did not reach a steady state during the exposure period, and was not completely eliminated even after 10 days of depuration, highlighting the importance of considering environmental hazards posed by pharmaceutical metabolites. • Bioconcentration and elimination of benzodiazepine temazepam in perch was examined. • Different importance of biotransformation pathways was registered compare to humans. • Temazepam metabolite (oxazepam) accumulated significantly in fish tissues. • Oxazepam did not reach steady state in fish after 10 days of exposure to parent drug. [ABSTRACT FROM AUTHOR]

The present study tested the biological consequences of exposure to a multimetal mixture as a multiple chemical stressor on Oncorhynchus mykiss at molecular, cellular, physiological and whole-organism levels and on biomarker responses of this fish during the depuration period. To represent environmentally relevant multiple chemical stressors, in our study, we used the mixture of Zn, Cu, Ni, Cr, Pb and Cd at the concentrations corresponding to Maximum-Permissible-Concentrations (MPCs) acceptable for the EU inland waters. This study was undertaken with a view to elucidate if changes in the MPC of the test mixture components (Ni, Pb, Cd) could cause significantly different biomarker responses in O. mykiss from those previously determined in the carnivorous and omnivorous fishes exposed to the mixture of the same metals but at different MPCs of Ni, Pb and Cd. This study has revealed that exposure to mixtures of metals at MPC produces genotoxic effects in fish blood erythrocytes and a lethargic effect on O. mykiss behaviour, and, also, significantly increases the levels of Cd, Cr and Ni accumulated in the gills tissue. O. mykiss successfully depurated Cr and Ni in less than 28 days, however, the level of Cd decreased by only approximately 40% over the same period. A significant capacity of O. mykiss to restore its DNA integrity (Comet assay) after exposure to metal mixtures was revealed. However, the 28-day recovery period proved to be insufficiently long for erythrocytes with nuclear abnormalities to recover to the unexposed level. In conclusion, changes in the MPCs of Ni, Pb and Cd in the test mixture produce biological effects similar to those previously determined in S. salar , R. rutilus and P. fluviatilis exposed to the mixture of the same metals but at lower MPCs of Ni and Pb and at higher MPC of Cd. • Multimetal mixtures at MPCs elicit genotoxic effects in O. mykiss blood erythrocytes. • Multimetal mixtures at MPCs had a lethargic effect on O. mykiss behaviour. • Treated fish tend to accumulate significantly high levels of Cd, Cr and Ni in gill. • Fish depurated Cr and Ni, Cd level decreased by 40% during the depuration period. • 28-day recovery period was insufficiently long for NAs to recover to control level. [ABSTRACT FROM AUTHOR]

A cost-effective, portable, ultra violet assisted vertical re-circulatory depuration system (UVDC) was developed and its effect on microbiological, heavy metal and proximate composition of Black clam (Villorita cyprinoides) was investigated. The process of depuration was found to be effective in reduction of total viable count by 1.8 log cfu g-1. Escherichia coli were within the permissible limit and both Vibrio cholera and V. parahaemolyticus were absent. The concentrations of heavy metals (Cd, Pb and Cu) were found to decrease by 40.44%, 96.51% and 34.50% respectively at the end of 48 h of depuration in UVDC. Significant reduction in protein, lipid, ash and glycogen contents were observed after the depuration process. The portability and easy to assemble nature of the system further improves its applicability as an onsite depuration unit which could be effectively utilized by the small-scale clam fishers/farmers depending on polluted waters for enhancing their income and livelihood. Image 1 • Portable UV assisted vertical, re-circulatory depuration system developed for bivalves. • Designed depuration unit significantly reduced heavy metal concentration in black clam. • After 48 h, E. coli was within the limit and V. cholera & V. parahaemolyticus were absent. • Easy to assemble, low cost depuration system for small scale clam fishers and farmers. [ABSTRACT FROM AUTHOR]

The uptake and depuration kinetics of diclofenac and carbamazepine alone at an environmentally relevant nominal concentration of 2 μg/L and in combination at a concentration ratio of 1:1 with total concentration of 4 μg/L were evaluated in Carassius carassius after 7 d uptake and depuration. Also, the biochemical effects of both drugs alone at nominal concentrations of 2 and 10 μg/L as well as in combination with total concentrations of 4 and 20 μg/L were investigated in Carassius carassius after 7 d exposure followed by 10 d recovery. In the single treatments, steady-state BCFs measured after the 7 d exposure were 73.05, 49.71, 38.01 and 24.93 L/kg for diclofenac and 9.25, 8.99, 5.29 and 4.11 L/kg for carbamazepine in the liver, brain, gill and muscle of Carassius carassius, respectively. Comparatively lower BCFs were measured in the tissues of Carassius carassius for both drugs in the combined treatments. Acetylcholinesterase activity in the brain was significantly induced by diclofenac while carbamazepine and the mixtures significantly inhibited it during all the exposure days as well as after the 10 d recovery in all treatments. This indicates that Carassius carassius could not recover from the neurotoxic effects caused by carbamazepine unlike the inductive effect caused by diclofenac which was recoverable after 10 days. A significant increase in the activities of 7-ethoxyresorufin O-deethylase and glutathione s-transferase for individual and mixed pharmaceuticals suggest that metabolism and detoxification of both drugs took place in the liver of Carassius carassius. Also, a significant increase in the activities of superoxide dismutase, catalase, glutathione reductase and malondialdehyde contents in the individual and mixture treatments mean that the antioxidant defence system of Carassius carassius was triggered to fight against oxidative stress but lipid peroxidation still occurred. However, Carassius carassius recovered from all these increases (superoxide dismutase, catalase, glutathione reductase and malondialdehyde) after the 10 d recovery, suggesting that oxidative damage is reversible. Our results indicate that both drugs at environmentally relevant concentrations might cause adverse effects in Carassius carassius and other fish species. Image 1 • Aqueous exposure of diclofenac and carbamazepine led to accumulation in the tissues of Carassius carassius. • BCFs ranged from 15.44 to 73.05 L/kg for diclofenac and 3.55–9.25 L/kg for carbamazepine.. • Carbamazepine inhibited acetylcholinesterase activity in the brain of the fish and was non-recoverable. • Both drugs were metabolised and detoxified in the liver of the fish. • Exposure to both drugs triggered the antioxidant defence system. [ABSTRACT FROM AUTHOR]

In aquatic organisms, dietary exposure to nanomaterials is not only one of the important uptake pathways, but it is also one method to assess the transmission risk of the food chain. To address this concern, we quantitatively investigated the accumulation and depuration of fullerenols in the tissues of zebrafish after exposure to fullerenols-contaminated Daphnia magna. After exposure to 13C-labelled fullerenol solution at a concentration of 2.5 mg/L for 72 h, the steady state concentration of fullerenols in D. magna was 31.20 ± 1.59 mg/g dry weight. During the 28 d uptake period for zebrafish, fullerenols in the tissues increased in a tissue- and day-dependent manner, and the major target tissues of fullerenols were the intestines and liver, followed by the gill, muscle, and brain. The kinetic parameters of uptake and depuration were also quantitatively analyzed. After depuration for 15 d, a certain amount of residual fullerenols remained in the tissues, especially the brain, where approximately 64 d may be needed to achieve 90% of the cumulative concentration depuration. The calculated distribution-based trophic transfer factors (TTF d values) (from 0.26 to 0.49) indicated that the tissue biomagnification of fullerenols by zebrafish through dietary exposure may not occur. Transmission electron microscopy (TEM) confirmed the presence of fullerenols in D. magna and the tissues of zebrafish. Our research data are essential for thoroughly understanding of the fate of nanoparticles through the dietary exposure pathway and directing future tissue bioeffect studies regarding target tissues for further research. Image 1 • Fullerenols can be absorbed into the tissues of zebrafish through dietary exposure in aquatic environments. • The accumulation and depuration kinetics of fullerenols in zebrafish tissues were quantitatively investigated. • The depuration rates of fullerenols in different tissues were found to be in the following order: gill > intestine > liver > muscle > brain. • Tissue biomagnification of fullerenols by zebrafish may not occur through dietary exposure. Fullerenols could be transferred from D. magna to zebrafish and further enter into tissues. The depuration rates of fullerenols in different tissues were found to be in the following order: gill > intestine > liver > muscle > brain. [ABSTRACT FROM AUTHOR]

Microplastic particles (MPs) from lipophilic polymers have been shown to efficiently accumulate hydrophobic organic contaminants (HOCs) in aquatic environments. MPs have, therefore, frequently been discussed as vectors for contaminants, enhancing HOC uptake by various organisms after ingestion followed by pollutant release; however, integrative models of sorption argue against this mechanism and even predict cleansing of pollutants from biological systems under particular circumstances. In order to experimentally investigate such a depuration mechanism, RTL-W1 cells were dosed with three 7-ethoxyresorufin- O -deethylase (EROD) inducers of distinct lipophilicity via the medium before adding both native and hexane-purified polyethylene MPs (20–25 μm) to the medium surface. EROD activity was significantly reduced in the presence of MP, the extent of which correlated with the inducers' lipophilicity (K OW) and thus affinity to MP. For hexane-purged MPs and TCDD (K OW = 6.8), MPs reduce the bioavailability by up to 79%; the effect was marginally weaker with benzo[ k ]fluoranthene (K OW = 6.11) and almost absent with β-Naphthoflavone (K OW = 4.68). Compared to hexane-purged MPs, native particles possessed slightly less detoxification potential. These experimental results corroborate theoretically predicted mechanisms of detoxification via MPs. Yet, it is unclear if, under corresponding conditions in the environment, MPs can compete with organismal tissues for highly lipophilic compounds and, if so, to which degree they may act as a sink reducing the amount of bioavailable pollutants in situ. However, the present results suggest that in scenarios where pollutant-free MPs interact with organisms that accumulated HOCs via other routes of uptake, qualitatively the presence of such a mechanism is likely. Image 1 • RTL-W1 cells were exposed to model pollutants with distinct lipophilicities. • Polyethylene microplastic particles (MPs) were added to the medium surface. • Amounts of inducers bioavailable to the cells were quantified via EROD-induction. • Considerable decreases (≤79%) by MPs were observed for highly lipophilic inducers. • MPs may mechanistically detoxify organisms similar to activated charcoal treatment. [ABSTRACT FROM AUTHOR]