Chronic toxicity, the development of adverse effects as a result of long term exposure to a contaminant or other stressor, is an important aspect of aquatic toxicology. [1] Adverse effects associated with chronic toxicity can be directly lethal but are more commonly sublethal, including changes in growth, reproduction, or behavior. Chronic toxicity is in contrast to acute toxicity, which occurs over a shorter period of time to higher concentrations. Various toxicity tests can be performed to assess the chronic toxicity of different contaminants, and usually last at least 10% of an organism's lifespan. [2] Results of aquatic chronic toxicity tests can be used to determine water quality guidelines and regulations for protection of aquatic organisms.
Chronic toxicity is the development of adverse effects as the result of long term exposure to a toxicant or other stressor. It can manifest as direct lethality but more commonly refers to sublethal endpoints such as decreased growth, reduced reproduction, or behavioral changes such as impacted swimming performance.
Chronic toxicity tests are performed to determine the long term toxicity potential of toxicants or other stressors, commonly to aquatic organisms. Examples of common aquatic chronic toxicity test organisms, durations, and endpoints include:
Results from chronic toxicity tests can be used to calculate values that can be used for determining water quality standards. These include:
The no observed effects concentration (NOEC) is determined as the highest tested concentration that shows no statistically significant difference from the control. The lowest observed effects concentration (LOEC) is the lowest concentration of those tested that produced a statistically significant difference from the control. NOECs and LOECs can be derived from both acute and chronic tests and are used by agencies to set water quality standards.
The maximum acceptable toxicant concentration (MATC) is calculated as the geometric mean of the NOEC and LOEC. MATC is sometimes called the chronic value (CV) and defined as “the concentration (threshold) at which chronic effects are first observed”. [3]
The predicted no effects concentration (PNEC) is calculated from toxicity tests to determine the concentration that is not thought to cause adverse effects to aquatic organisms. [4] Determination of aquatic PNEC values requires toxicity test results from freshwater fish (e.g. ‘‘Pimephales promelas’’), freshwater invertebrates (e.g. ‘‘Daphnia magna’’), and freshwater algae (e.g. ‘‘Raphidocelis subcapitata’’) The probable effects concentration (PEC), the concentration predicted to be in the environment, is compared with the PNEC in risk assessment. The PEC takes into account both acute and chronic exposures to toxicants.
The acute to chronic ratio (ACR) allows for an estimation of Chronic toxicity using acute toxicity data. It is calculated by dividing the LC50 by the MATC. The inverse of this (MATC/LC50) is termed the application factor (AF). AFs can be used when chronic toxicity data is not known for a specific species.
The chronic toxicity of toxicants is useful information to know in determining water quality guidelines, but this information is not always easily obtained. Chronic toxicity tests can be costly and difficult, due to challenges in keeping control organisms alive, maintaining water quality, retaining constant chemical exposures, and the sheer time required for tests. Because of this, acute toxicity tests are more commonly employed, and ACRs and AFs are used to estimate chronic toxicity of toxicants to organisms.
There are many factors that can increase or decrease the toxicity of toxicants or stressors, making interpretation of test results difficult. These can be chemical, biological, or toxicological.
Water chemistry plays an important role in the toxicity of certain toxicants. This includes pH, salinity, water hardness, conductivity, temperature, and amounts of dissolved organic carbon (DOC) For instance, the toxicity of copper is decreased with increasing amounts of DOC, as described by the biotic ligand model (BLM). [5]
Chronic toxicity will vary with differences in organisms, including species, size, and age. Certain species are more susceptible to toxic effects, as shown in species sensitivity distributions (SSDs). Certain life stages are more susceptible to adverse effects, which is why early life stage (ELS) toxicity tests are performed for certain aquatic species. In addition, other physical factors, like organism size, can lead to differences in response to toxicants.
Water quality guidelines are determined based on the results of both acute and chronic toxicity tests. Criteria maximum concentrations (CMCs) are obtained from acute toxicity tests, whereas criteria continuous concentrations (CCCs) are obtained from chronic toxicity tests. [6] They are values determined by the U.S. EPA to be protective of aquatic organisms.
Toxicity is the degree to which a chemical substance or a particular mixture of substances can damage an organism. Toxicity can refer to the effect on a whole organism, such as an animal, bacterium, or plant, as well as the effect on a substructure of the organism, such as a cell (cytotoxicity) or an organ such as the liver (hepatotoxicity). Sometimes the word is more or less synonymous with poisoning in everyday usage.
Aquatic toxicology is the study of the effects of manufactured chemicals and other anthropogenic and natural materials and activities on aquatic organisms at various levels of organization, from subcellular through individual organisms to communities and ecosystems. Aquatic toxicology is a multidisciplinary field which integrates toxicology, aquatic ecology and aquatic chemistry.
Ecotoxicology is the study of the effects of toxic chemicals on biological organisms, especially at the population, community, ecosystem, and biosphere levels. Ecotoxicology is a multidisciplinary field, which integrates toxicology and ecology.
Measures of pollutant concentration are used to determine risk assessment in public health.
Ecotoxicity, the subject of study in the field of ecotoxicology, refers to the biological, chemical or physical stressors that affect ecosystems. Such stressors could occur in the natural environment at densities, concentrations, or levels high enough to disrupt natural biochemical and physiological behavior and interactions. This ultimately affects all living organisms that comprise an ecosystem.
Environmental toxicology is a multidisciplinary field of science concerned with the study of the harmful effects of various chemical, biological and physical agents on living organisms. Ecotoxicology is a subdiscipline of environmental toxicology concerned with studying the harmful effects of toxicants at the population and ecosystem levels.
The Biotic Ligand Model (BLM) is a tool used in aquatic toxicology that examines the bioavailability of metals in the aquatic environment and the affinity of these metals to accumulate on gill surfaces of organisms. BLM depends on the site-specific water quality including such parameters as pH, hardness, and dissolved organic carbon. In this model, lethal accumulation values are used to be predictive of lethal concentration values that are more universal for aquatic toxicology and the development of standards. Collection of water chemistry parameters for a given site, incorporation of the data into the BLM computer model and analysis of the output data is used to accomplish BLM analysis. Comparison of these values derived from the model, have repeatedly been found to be comparable to the results of lethal tissue concentrations from acute toxicity tests. The BLM was developed from the gill surface interaction model (GSIM) and the free ion activity model (FIAM). Both of these models also address how metals interact with organisms and aquatic environments. Currently, the United States Environmental Protection Agency (EPA) uses the BLM as a tool to outline Ambient Water Quality Criteria (AWQC) for surface water. Because BLM is so useful for investigation of metals in surface water, there are developmental plans to expand BLM for use in marine and estuarine environments.
A mode of toxic action is a common set of physiological and behavioral signs that characterize a type of adverse biological response. A mode of action should not be confused with mechanism of action, which refer to the biochemical processes underlying a given mode of action. Modes of toxic action are important, widely used tools in ecotoxicology and aquatic toxicology because they classify toxicants or pollutants according to their type of toxic action. There are two major types of modes of toxic action: non-specific acting toxicants and specific acting toxicants. Non-specific acting toxicants are those that produce narcosis, while specific acting toxicants are those that are non-narcotic and that produce a specific action at a specific target site.
Fish acute toxicity syndrome (FATS) is a set of common chemical and functional responses in fish resulting from a short-term, acute exposure to a lethal concentration of a toxicant, a chemical or material that can produce an unfavorable effect in a living organism. By definition, modes of action are characterized by FATS because the combination of common responses that represent each fish acute toxicity syndrome characterize an adverse biological effect. Therefore, toxicants that have the same mode of action elicit similar sets of responses in the organism and can be classified by the same fish acute toxicity syndrome.
Tissue residue is the concentration of a chemical or compound in an organism's tissue or in a portion of an organism's tissue. Tissue residue is used in aquatic toxicology to help determine the fate of chemicals in aquatic systems, bioaccumulation of a substance, or bioavailability of a substance, account for multiple routes of exposure, and address an organism's exposure to chemical mixtures. A tissue residue approach to toxicity testing is considered a more direct and less variable measure of chemical exposure and is less dependent on external environmental factors than measuring the concentration of a chemical in the exposure media.
Toxicodynamics, termed pharmacodynamics in pharmacology, describes the dynamic interactions of a toxicant with a biological target and its biological effects. A biological target, also known as the site of action, can be binding proteins, ion channels, DNA, or a variety of other receptors. When a toxicant enters an organism, it can interact with these receptors and produce structural or functional alterations. The mechanism of action of the toxicant, as determined by a toxicant’s chemical properties, will determine what receptors are targeted and the overall toxic effect at the cellular level and organismal level.
Ecological death is the inability of an organism to function in an ecological context, leading to death. This term can be used in many fields of biology to describe any species. In the context of aquatic toxicology, a toxic chemical, or toxicant, directly affects an aquatic organism but does not immediately kill it; instead it impairs an organism's normal ecological functions which then lead to death or lack of offspring. The toxicant makes the organism unable to function ecologically in some way, even though it does not suffer obviously from the toxicant. Ecological death may be caused by sublethal toxicological effects that can be behavioral, physiological, biochemical, or histological.
The maximum acceptable toxicant concentration (MATC) is a value that is calculated through aquatic toxicity tests to help set water quality regulations for the protection of aquatic life. Using the results of a partial life-cycle chronic toxicity test, the MATC is reported as the geometric mean between the No Observed Effect Concentration (NOEC) and the lowest observed effect concentration (LOEC).
An early life stage (ELS) test is a chronic toxicity test using sensitive early life stages like embryos or larvae to predict the effects of toxicants on organisms. ELS tests were developed to be quicker and more cost-efficient than full life-cycle tests, taking on average 1–5 months to complete compared to 6–12 months for a life-cycle test. They are commonly used in aquatic toxicology, particularly with fish. Growth and survival are the typically measured endpoints, for which a Maximum Acceptable Toxicant Concentration (MATC) can be estimated. ELS tests allow for the testing of fish species that otherwise could not be studied due to length of life, spawning requirements, or size. ELS tests are used as part of environmental risk assessments by regulatory agencies including the U.S. Environmental Protection Agency (EPA) and Environment Canada, as well as the Organisation for Economic Co-operation and Development (OECD).
The olfactory system is the system related to the sense of smell (olfaction). Many fish activities are dependent on olfaction, such as: mating, discriminating kin, avoiding predators, locating food, contaminant avoidance, imprinting and homing. These activities are referred to as “olfactory-mediated.” Impairment of the olfactory system threatens survival and has been used as an ecologically relevant sub-lethal toxicological endpoint for fish within studies. Olfactory information is received by sensory neurons, like the olfactory nerve, that are in a covered cavity separated from the aquatic environment by mucus. Since they are in almost direct contact with the surrounding environment, these neurons are vulnerable to environmental changes. Fish can detect natural chemical cues in aquatic environments at concentrations as low as parts per billion (ppb) or parts per trillion (ppt).
The predicted no-effect concentration (PNEC) is the concentration of a chemical which marks the limit at which below no adverse effects of exposure in an ecosystem are measured. PNEC values are intended to be conservative and predict the concentration at which a chemical will likely have no toxic effect. They are not intended to predict the upper limit of concentration of a chemical that has a toxic effect. PNEC values are often used in environmental risk assessment as a tool in ecotoxicology. A PNEC for a chemical can be calculated with acute toxicity or chronic toxicity single-species data, Species Sensitivity Distribution (SSD) multi-species data, field data or model ecosystems data. Depending on the type of data used, an assessment factor is used to account for the confidence of the toxicity data being extrapolated to an entire ecosystem.
Toxicological databases are large compilations of data derived from aquatic and environmental toxicity studies. Data is aggregated from a large number of individual studies in which toxic effects upon aquatic and terrestrial organisms have been determined for different chemicals. These databases are then used by toxicologists, chemists, regulatory agencies and scientists to investigate and predict the likelihood that an organic or inorganic chemical will cause an adverse effect on exposed organisms.
The acute to chronic ratio (ACR) uses acute toxicity data to gauge the chronic toxicity (MATC) of a chemical of interest to an organism. The science behind determining a safe concentration to the environment is imperfect, statistically limited, and resource intensive. There is an unfilled demand for the rapid assessment of different chemical toxicity to many different organisms. The ACR is a proposed solution to this demand.
Toxic units (TU) are used in the field of toxicology to quantify the interactions of toxicants in binary mixtures of chemicals. A toxic unit for a given compound is based on the concentration at which there is a 50% effect for a certain biological endpoint. One toxic unit is equal to the EC50 for a given endpoint for a specific biological effect over a given amount of time. Toxic units allow for the comparison of the individual toxicities of a binary mixture to the combined toxicity. This allows researchers to categorize mixtures as additive, synergistic or antagonistic. Synergism and antagonism are defined by mixtures that are more or less toxic than predicted by the sum of their toxic units.
Diafenthioron is a pesticide, specifically an insecticide. It is a chemical compound which belongs to the thiourea group. Diafenthiuron is sold under the brand names Derby, Diron, Pegasus, Polar and Polo.