RESUMEN
Phenanthrene (PHE) and Cu are two contaminants commonly co-occurring in marine and freshwater environments. Mixtures of PHE and Cu have been reported to induce more-than-additive lethality in the amphipod, Hyalella azteca, a keystone aquatic invertebrate, yet little is understood regarding the interactive toxic mechanisms that mediate more-than-additive toxicity. Understanding the interactions among toxic mechanisms among Cu and PHE will allow for better predictive power in assessing the ecological risks of Cu-PHE mixtures in aquatic environments. Here we use behavioural impairment to help understand the toxic mechanisms of Cu, PHE, and Cu-PHE mixture toxicity in the aquatic amphipod crustacean, Hyalella azteca. Our principal objective was to link alterations in activity and ventilation with respiratory rates, oxidative stress, and neurotoxicity in adult H. azteca. Adult amphipods were used for all toxicity tests. Amphipods were tested at sublethal exposures of 91.8- and 195-µgL(-1) Cu and PHE, respectively, and a Cu-PHE mixture at the same concentrations for 24h. Neurotoxicity was measured as acetylcholinesterase (AChE) activity, where malathion was used as a positive control. Oxidative stress was measured as reactive oxygen species (ROS) production. Phenanthrene-exposed amphipods exhibited severe behavioural impairment, being hyperstimulated to the extent that they were incapable of coordinating muscle movements. In addition, respiration and AChE activity in PHE-exposed amphipods were increased and reduced by 51% and 23% respectively. However, ROS did not increase following exposure to phenanthrene. In contrast, Cu had no effect on amphipod behaviour, respiration or AChE activity, but did lead to an increase in ROS. However, co-exposure to Cu antagonized the PHE-induced reduction in ventilation and negated any increase in respiration. The results suggest that PHE acts like an organophosphate pesticide (e.g., malathion) in H. azteca following 24h sublethal exposures, and that AChE inhibition is the likely mechanism by which PHE alters H. azteca behaviour. However, interactive aspects of neurotoxicity do not account for the previously observed more-than-additive mortality in H. azteca following exposure to Cu-PHE mixtures.
Asunto(s)
Anfípodos/fisiología , Complejos de Coordinación/toxicidad , Cobre/toxicidad , Insecticidas/toxicidad , Fenantrenos/toxicidad , Contaminantes Químicos del Agua/toxicidad , Acetilcolinesterasa/metabolismo , Anfípodos/efectos de los fármacos , Animales , Conducta Animal/efectos de los fármacos , Encéfalo/enzimología , Complejos de Coordinación/química , Cobre/química , Insecticidas/química , Fenantrenos/química , Especies Reactivas de Oxígeno/metabolismo , Frecuencia Respiratoria/efectos de los fármacos , Pruebas de ToxicidadRESUMEN
Mixtures of metals and polycyclic aromatic hydrocarbons (PAHs) are commonly found in aquatic environments. Emerging reports have identified that more-than-additive mortality is common in metal-PAH mixtures. Individual aspects of PAH toxicity suggest they may alter the accumulation of metals and enhance metal-derived reactive oxygen species (ROS). Redox-active metals (e.g., Cu and Ni) are also capable of enhancing the redox cycling of PAHs. Accordingly, we explored the mutual effects redox-active metals and PAHs have on oxidative stress, and the potential for PAHs to alter the accumulation and/or homeostasis of metals in juvenile Hyalella azteca. Amphipods were exposed to binary mixtures of Cu, Cd, Ni, or V, with either phenanthrene (PHE) or phenanthrenequinone (PHQ). Mixture of Cu with either PAH produced striking more-than-additive mortality, whereas all other mixtures amounted to strictly additive mortality following 18-h exposures. We found no evidence to suggest that interactive effects on ROS production were involved in the more-than-additive mortality of Cu-PHE and Cu-PHQ mixtures. However, PHQ increased the tissue concentration of Cu in juvenile H. azteca, providing a potential mechanism for the observed more-than-additive mortality.
Asunto(s)
Anfípodos/efectos de los fármacos , Metales/toxicidad , Estrés Oxidativo/efectos de los fármacos , Hidrocarburos Policíclicos Aromáticos/toxicidad , Anfípodos/metabolismo , Animales , Cobre/farmacocinética , Cobre/toxicidad , Ecotoxicología/métodos , Metales/farmacocinética , Oxidación-Reducción , Fenantrenos/farmacocinética , Fenantrenos/toxicidad , Hidrocarburos Policíclicos Aromáticos/farmacocinética , Especies Reactivas de Oxígeno/metabolismo , Tasa de Supervivencia , Contaminantes Químicos del Agua/farmacocinética , Contaminantes Químicos del Agua/toxicidadRESUMEN
Mixtures of metals and polycyclic aromatic hydrocarbons (PAHs) occur ubiquitously in aquatic environments, yet relatively little is known regarding their potential to produce non-additive toxicity (i.e., antagonism or potentiation). A review of the lethality of metal-PAH mixtures in aquatic biota revealed that more-than-additive lethality is as common as strictly additive effects. Approaches to ecological risk assessment do not consider non-additive toxicity of metal-PAH mixtures. Forty-eight-hour water-only binary mixture toxicity experiments were conducted to determine the additive toxic nature of mixtures of Cu, Cd, V, or Ni with phenanthrene (PHE) or phenanthrenequinone (PHQ) using the aquatic amphipod Hyalella azteca. In cases where more-than-additive toxicity was observed, we calculated the possible mortality rates at Canada's environmental water quality guideline concentrations. We used a three-dimensional response surface isobole model-based approach to compare the observed co-toxicity in juvenile amphipods to predicted outcomes based on concentration addition or effects addition mixtures models. More-than-additive lethality was observed for all Cu-PHE, Cu-PHQ, and several Cd-PHE, Cd-PHQ, and Ni-PHE mixtures. Our analysis predicts Cu-PHE, Cu-PHQ, Cd-PHE, and Cd-PHQ mixtures at the Canadian Water Quality Guideline concentrations would produce 7.5%, 3.7%, 4.4% and 1.4% mortality, respectively.
Asunto(s)
Anfípodos/efectos de los fármacos , Fenómenos Ecológicos y Ambientales , Metales/toxicidad , Hidrocarburos Policíclicos Aromáticos/toxicidad , Pruebas de Toxicidad , Animales , Biota , Canadá , Factores de RiesgoRESUMEN
Mixtures of metals and polycyclic aromatic hydrocarbons (PAHs) occur ubiquitously in aquatic environments, yet relatively little is known regarding their combined toxicities. Emerging reports investigating the additive mortality in metal-PAH mixtures have indicated that more-than-additive effects are equally as common as strictly-additive effects, raising concern for ecological risk assessment typically based on the summation of individual toxicities. Moreover, the current separation of focus between in vivo and in vitro studies, and fine- and coarse-scale endpoints, creates uncertainty regarding the mechanisms of co-toxicity involved in more-than-additive effects on whole organisms. Drawing from literature on metal and PAH toxicity in bacteria, protozoa, invertebrates, fish, and mammalian models, this review outlines several key mechanistic interactions likely to promote more-than-additive toxicity in metal-PAH mixtures. Namely, the deleterious effects of PAHs on membrane integrity and permeability to metals, the potential for metal-PAH complexation, the inhibitory nature of metals to the detoxification of PAHs via the cytochrome P450 pathway, the inhibitory nature of PAHs towards the detoxification of metals via metallothionein, and the potentiated production of reactive oxygenated species (ROS) in certain metal (e.g. Cu) and PAH (e.g., phenanthrenequinone) mixtures. Moreover, the mutual inhibition of detoxification suggests the possibility of positive feedback among these mechanisms. The individual toxicities and interactive aspects of contaminant transport, detoxification, and the production of ROS are herein discussed.
Asunto(s)
Metales/toxicidad , Hidrocarburos Policíclicos Aromáticos/toxicidad , Contaminantes Químicos del Agua/toxicidad , Animales , Sinergismo FarmacológicoRESUMEN
Microcystin (MC) concentrations were measured in the alimentary tract, digestive gland, and remaining visceral mass of adult pulmonate snails (Lymnaea stagnalis) exposed to cyanobacteria known to contain MC. The highest proportion of total body MC content was measured within the alimentary tract (83%), though an appreciable proportion (17%) was also found within the digestive gland tissue. This provides conclusive evidence for the limited digestion of toxic cyanobacteria and subsequent uptake and accumulation of MC by the digestive gland of L. stagnalis. Additionally, pure microcystin-LR was orally administered to adult L. stagnalis to investigate the potential for toxic effects. Exposure to microcystin-LR induced histopathological alterations of the digestive glands consistent with those reported elsewhere for mammals and fish, indicating a common mode of toxicity to both vertebrates and invertebrates.
Asunto(s)
Toxinas Bacterianas/farmacocinética , Inhibidores Enzimáticos/farmacocinética , Tracto Gastrointestinal/metabolismo , Lymnaea/metabolismo , Microcistinas/farmacocinética , Administración Oral , Animales , Toxinas Bacterianas/toxicidad , Cianobacterias/crecimiento & desarrollo , Cianobacterias/metabolismo , Inhibidores Enzimáticos/toxicidad , Eutrofización , Agua Dulce/microbiología , Tracto Gastrointestinal/efectos de los fármacos , Microcistinas/toxicidad , Distribución TisularRESUMEN
It has been suggested that little to no microcystin (MC), a cyanobacterial hepatotoxin, accumulates within freshwater pulmonate snails because the toxin is associated primarily with undigested gut contents that are eliminated from the animal via egestion. To test this, Lymnaea stagnalis exposed to MC-containing cyanobacteria were placed into toxin-free environments and sampled over short (24 h at 21 degrees C) and long (30 d at 22 and 10 degrees C) time periods. Within 8 h after being removed from exposure to microcystin-containing phytoplankton, the gizzard and cecal string fractions of the feces were eliminated, accounting for 57% of the initial MC concentration. However, detectable concentrations remained beyond 24 h, likely in association with the digestive-gland contents, which can be retained up to 100 h. Long-term MC loss was biphasic at two ambient temperatures. The greatest change (fast phase) occurred over the first 3 d after exposure. By 6 d, the cumulative MC loss from L. stagnalis was 80 and 95% at 10 and 22 degrees C, respectively. Toxin loss over this period was attributed to egestion of indigestible cells/colonies from gizzard and cecum, as well as elimination of unassimilated MC-laden fragments and vacuolate excretion of residues from the digestive gland. The fast-phase depuration rate constant was significantly higher at 22 than at 10 degrees C, indicating an influence of ambient temperature on the rate of toxin loss from pulmonate snails. Depuration continued at slower rates until 30 d, when most (97.5 and 99.5% at 10 and 22 degrees C, respectively) of the initial MC was eliminated.
Asunto(s)
Toxinas Bacterianas/farmacocinética , Tracto Gastrointestinal/metabolismo , Lymnaea/metabolismo , Péptidos Cíclicos/farmacocinética , Animales , Cianobacterias , Eutrofización , Agua Dulce , Microcistinas , TemperaturaRESUMEN
Cyanobacteria possess many adaptations to develop population maxima or "blooms" in lakes and reservoirs. A potential consequence of freshwater blooms of many cyanobacterial species is the production of potent toxins, including the cyclic hepatotoxins, microcystins (MCs). Approximately 70 MC variants have been isolated. Their toxicity to humans and other animals is well studied, because of public health concerns. This review focuses instead on the production and degradation of MCs in freshwater environments and their effects on aquatic organisms. Genetic research has revealed the existence of MC-related genes, yet the expression of these genes seems to be regulated by complex mechanisms and is influenced by environmental factors. In natural water bodies, the species composition of cyanobacterial communities and the ratio of toxic to nontoxic species and strains are largely responsible for total toxin production. Cyanobacteria play vital roles in aquatic food webs, yet production, accumulation, and toxicity patterns of MCs within aquatic food webs remain obscure.
Asunto(s)
Toxinas Bacterianas/efectos adversos , Cianobacterias/patogenicidad , Agua Dulce/microbiología , Animales , Toxinas Bacterianas/química , Toxinas Bacterianas/genética , Cianobacterias/genética , Ambiente , Peces , Cadena Alimentaria , Genes Bacterianos , Humanos , Invertebrados , Microbiología del AguaRESUMEN
Northern pike (Esox lucius) are often considered to be specialist piscivores, but under some circumstances will continue to eat invertebrates as adults. To examine effects of fish assemblage composition on the trophic ecology of pike, we combined stable isotope analysis (SIA) of carbon and nitrogen and stomach content analysis (SCA) on pike from five lakes in northern Alberta, three of which contain only pike ("pike-only") and two that also contain yellow perch (Perca flavescens) or white sucker (Catostomus commersoni) ("pike-other"). Fish were more important as prey and empty stomachs, which often characterize piscivores, were significantly more frequent in pike-other than in pike-only lakes. However, even though invertebrates were more important for pike in pike-only lakes, SIA and SCA indicated that invertebrates were also an important component of pike diets in pike-other lakes. SIA and SCA also revealed considerable intrapopulation variation in trophic ecology, with individuals in some populations differing by as much as two trophic levels. Comparisons of stomach contents and isotope signatures of the same fish suggested that within these variable populations, specialization on invertebrates or fish was a long-term trait of some individuals. SIA indicated that trophic position increased and diets shifted to a greater importance of littoral prey as pike grew in pike-only lakes, but not in lakes with other fish present. Trophic adaptability in northern pike is expressed at both the population level, where the trophic ecology is sensitive to differences in prey regimes, and at the organismal level, in the form of intrapopulation variation and individual specialization.