32 Contaminant behaviour, exposure, uptake and impact of Marine Pollution
All contaminants, whether inorganic or organic, will ultimately be distributed through ecosystems and stored in various compartments (e.g. sediments and body tissues). The environmental fate of contaminants results from their chemical properties, and it is the fugacity (sometimes described as the potential to move between media) of a substance that determines its likely distribution after its release into the environment (e.g. water or lipid solubility, vapour pressure) as well as the hydrodynamic and physiological processes occurring in those ecosystems (e.g. winds, currents, flow rate, upwelling, and sedimentation).

‘Jellyfish Floating Amid Ocean Debris’ by Nadejda Bostanova is used under a Pexels License
We tend to focus our sampling on the various compartments of water, biota, and sediment. Once compartmentalised, the duration of storage will depend on the stability of the conditions in that compartment. For example, when sediments are disturbed, stored contaminants can be remobilised back into the water column, or if an organism dies the contaminants that were taken up and stored in its body will become available to detritivores and through trophic levels thereafter.
Ecotoxicological studies help us to understand how an organism interacts with a contaminant and identify measurable stress responses.
This text from “Marine Pollution in Context” In: Reichelt-Brushett, A. (eds) “Marine Pollution – Monitoring, Management and Mitigation” 2023, by Amanda Reichelt-Brushett, which is licensed under CC BY 4.0
Exposure and uptake pathways
Bioconcentration: The process whereby chemicals enter aquatic organisms through the gills or epithelial tissue directly from the water (or surrounding environmental medium) and become more concentrated in the organism than in the surrounding environmental medium (water, soil, etc.).
Bioaccumulation: Chemical uptake by an organism, attributable to both bioconcentration and dietary accumulation. Bioaccumulation is related to organism-specific rates of uptake, metabolism, and elimination, and occurs when a substance is absorbed at a faster rate than it is lost.
Biomagnification: The process whereby tissue concentrations of a bioaccumulated chemical increase with successively higher levels in a food chain (at least two trophic levels). This phenomenon is rare; however, those specific contaminants that do biomagnify pose serious environmental problems, and consequently, receive great publicity. Contaminants known to biomagnify include:
- Chlorinated hydrocarbons;
- Insecticides (e.g. DDT group and cyclodienes—dieldrin);
- Non-insecticides (e.g. PCBs—hydraulic fluids, heat-transfer fluids); and
- Some organometallic compounds (e.g. methylmercury [MeHg], tributyltin [TBT]).
These contaminants characteristically have a high lipid solubility and therefore, a strong affinity to accumulate in biological tissue with high-fat content (including adipose tissue/blubber, white muscle, and some organs). They are stable and persistent within the organism, and accumulation can lead to disease and mortality in higher order predators.
Bioavailability is another common term that refers to the fraction of an element (or compound) that is available to be taken up by an organism. The entry pathway of a contaminant into an organism (e.g. via water, sediment, food, etc.) will also influence the bioavailability. Metals that are weakly bound to sediment particles are bioavailable. However, some contaminants are very strongly adsorbed to sediment particles or bound within the lattice structure of the particle: they will not be reactive within the organism and will likely pass through the organism with the particle.
This text is from “Collecting, Measuring, and Understanding Contaminant Concentrations in the Marine Environment” In: Reichelt-Brushett, A. (eds) “Marine Pollution – Monitoring, Management and Mitigation.” 2023, by Reichelt-Brushett, A, which is licensed under CC BY 4.0.
Factors influencing toxicity
The concentration of a chemical is one of the more obvious factors that will affect its toxicity. You may have heard the historic quote from Paracelsus (1493‒1541), who expressed:
“All substances are poisons; there is none that is not a poison. The right dose differentiates a poison and a remedy.”
However, many other environmental, physiological, biological, and chemical factors influence the toxicity of a chemical (e.g. Charition et al. 2010; de Almeida Rodrigues et al. 2022). More specifically:
Temperature: the toxicity of many substances differs with temperature, however, there is no general rule as to whether a higher or lower temperature will elicit a higher toxicity. For example, some metals are more toxic in tropical marine ecosystems than in temperate or polar regions, whereas for other metals this is reversed (Chapman et al. 2006). This makes the extrapolation of toxicity data from different climatic regions unreliable. This is one reason that some countries such as Canada and the USA have requirements to use toxicity data for endemic species. This approach is possible for North American and European countries because most of the test organisms used in toxicity tests originated from those regions. However, in other countries with smaller populations, different climates, and/ or different ecosystems and species, this approach is not logistically possible, and instead toxicity data generated using non-endemic species must be relied upon.
pH: affects solubility, and therefore bioavailability, of contaminants such as metals. Generally, a decrease in pH increases the toxicity of metals as they become more bioavailable. Since marine waters are buffered, they resist changes in pH (to a point).
Salinity: can decrease the toxicity of chemicals by decreasing their aqueous solubility or changing their chemical form, although this depends on the type and concentration of other competing substances such as dissolved organic compounds (e.g. Hall and Anderson 2008).
Suspended sediment: may increase toxicity (for example by providing a surface for contaminants to bind to, allowing uptake of contaminants by some organisms), but can also decrease toxicity (e.g. by decreasing the bioavailability of hydrophobic chemicals to aquatic organisms). This largely depends on the type of contaminant and the type of sediment. Suspended sediments may also act as a stressor in their own right.
Dissolved organic carbon: may decrease toxicity by decreasing a chemical’s aqueous solubility, and its ability to pass through membranes or bioavailability.
Previous exposure/resistance: populations or strains of species may develop resistance to toxicants, so that considerable differences in sensitivity may exist within one species. For instance, species in areas with naturally elevated concentrations of metals may become more tolerant to those metals.
Organism life stage: generally the early and oldest life stages are the most sensitive to the harmful effects of chemicals.
Duration of exposure: generally a longer period of exposure will result in adverse effects at lower concentrations of a toxicant than the same effects measured after a short period of exposure.
This text is from “Assessing Organism and Community Responses” In: Reichelt-Brushett, A. (eds) “Marine Pollution – Monitoring, Management and Mitigation” 2023, by Amanda Reichelt-Brushett, Pelli L. Howe, Anthony A. Chariton, Michael St. J. Warne, which is licensed under CC BY 4.0
Contaminants in the marine environment: types, common sources, and general factors influencing impact and potential as pollutants
The table below summarises common contaminants in the marine environment: types, common sources, and general factors influencing impact and potential as pollutants.
| Contaminant class | Examples | Examples of sources | General impacts and influencing factors |
|---|---|---|---|
| Trace elements | Arsenic (As), cadmium (Cd), copper (Cu), iron (Fe), nickel (Ni), silver (Ag), zinc (Zn); rare earth metals of increasing concern, e.g. lithium (Li), caesium (Cs), and yttrium (Y) | Antifouling paints, batteries, electronics, fuels, building materials, mining wastes (small and large scale, terrestrial, deep sea; marine tailings disposal), agricultural and urban runoff, industrial effluents, landfill leachate, erosion, atmospheric deposition, shipping accidents, and operational ship discharges | Many essential at low concentrations, highly toxic at elevated levels; natural variation due to local geology; solubility and toxicity strongly influenced by water physicochemistry (i.e. pH, salinity, complexing capacity, and dissolved oxygen), competition with essential elements affects structure and function of biomolecules and physiological processes. Biological detoxification and depuration processes exist |
| Organometallic compounds | Mono, di and tri-butyltin (TBT), methylmercury (CH3Hg+), and some pesticides | Agricultural runoff and waste, industrial effluents, mining wastes, and antifouling paints | Organic forms of some metals are more toxic than their inorganic counterparts; may be direct inputs or naturally formed after metal introduction—influenced by type and abundance of organic ligands, microbial communities (i.e. methylating bacteria), and oxygenation |
| Agricultural chemicals | Insecticides, herbicides, fungicides, and other specific pesticides and disinfectants | Agricultural runoff and waste, aquaculture, and mariculture | Synthesised for biocidal properties (many non-specific) similar activity in receiving environment; continuing legacy of older formulations (e.g. DDT) that are extremely persistent compared to most modern formulations |
| Nutrients | Nitrogen (N) and phosphorous (P) | Fertilisers, sewage, urban and agricultural runoff, aquaculture, and mariculture | Enrichment in plant nutrients increases primary productivity; eutrophication and associated changes to ecosystem structure and function (e.g. increased crown of thorns starfish outbreaks, algal blooms produce toxins and cause deoxygenation); influenced by water exchange, limiting nutrients, nutrient cycling, and type and resilience of ecosystem (e.g. reefs requiring oligotrophic conditions will be more significantly affected than a mesotrophic system) |
| Persistent organic and halogenated chemicals | Dioxin, fluorocarbons, organochlorines, organophosphates, organobromines, etc | By-products of fuel and waste combustion and industrial processes (e.g. paper and plastic manufacturing), flame retardants, fire-fighting foam, non-stick coatings, landfill leachates, agricultural runoff, and atmospheric deposition | Extremely Persistent chemical structures with many now banned in many countries. They are mostly lipophilic and bioaccumulate and biomagnify. There are limited biological detoxification and degradation pathways |
| Hydrocarbons and dispersants | Oil, gas, and some petroleum products | Shipping operations and accidents and off-shore extraction and processing | Comprised of C and H with high molecular stability and lipophilicity and are physical and chemical toxicity. The extent of pollution depends on amount, type of hydrocarbon (i.e. volatility, viscosity) and the hydrodynamics of the spill area |
| – | Dispersants | Oil spill remediation | Used to break oil into droplets which can be easily dispersed in water, and enhance biodegradation; toxic to pelagic/benthic organisms; should not be used in shallow or ecologically sensitive waters (e.g. reefs, fishing areas, and marine parks) |
| Dissolved gases | Carbon dioxide (CO2) | Fossil fuel emissions, agriculture, and atmospheric equilibration | Ocean acidification depending on carbonate biogeochemistry (pH buffering capacity). May cause decreased carbonate saturation and thus reduce biogenic calcification |
| Pharmaceuticals | Antibiotics, antidepressants, blood pressure and diabetes medication, birth control, anti-bacterial agents, illicit drugs, and veterinary products | Sewage outfall (treated and untreated) and biosolids, agricultural runoff, wastewater discharges, aquaculture, and mariculture | Sewage treatment methods often ineffective. Concentrations in the environment reflect variable spatial and temporal usage trends. May cause endocrine disruption (e.g. feminisation of male organisms). The pollution potential depends on the mode of action, concentration, and stability of the compound as well as potential mixtures |
| Personal care and household products | Soaps; sunscreens; disinfectants; surfactants; nanoparticles (e.g. zinc and titanium dioxide) | Sewage; recreation; wastewater discharges; industrial cleaning; operational ship discharge | High inputs into coastal zones which are sensitive breeding/nursery grounds for many species (not significant in open ocean). Generally slow to degrade with potential photochemical reactions and toxic degradation products. Specific persistence and toxicity vary between compounds |
| Pathogens | Parasites, viruses, protozoans, and bacteria | Untreated sewage, agricultural runoff, aquaculture, and mariculture | Introduction of new diseases, shifts in symbiotic microbial populations, and reduced resilience to existing diseases which can be exacerbated by deteriorating water quality |
| Plastics and debriss | Plastic bottles; packaging and general rubbish; microplastics; fishing nets and lines; timber; metal; other building materials | Dumping, litter, natural disasters, commercial fishing, aquaculture, and shipping accidents | Pollution potential depends on the size, shape, and buoyancy of the material. They are typically persistent impacting organisms by ingestion, entanglement, and release of toxicants (e.g. PCBs). May cause reduced air–water and sediment–water oxygen exchange and act as hosts for translocation and introduction of species attached to drifting plastics |
| Sediment | Soil; clay; sand; fine sediment | Dredging, port construction, direct dumping of dredged sediment, catchment clearing, poor quality riparian vegetation, high rainfall, and erosion | Various particle sizes and settling rates. Causes high turbidity, smothering, and reduced light penetration. The impacts are related to the frequency, intensity, and duration of exposure and associated contaminant toxicity |
| Other | Radioactivity and explosives, | Conflict, accidents, weapons testing and use, and emissions from historical ocean dumping | May be non-ionising (low-energy photons) (e.g. light, radio waves) or ionising (high energy alpha, beta, gamma particles). Results in free radical production (e.g. OH−) that is highly reactive. The impacts are influenced by radiation type and decay rate (half-life) |
| – | Noise | Shipping, military operations, seismic surveys; deep sea mining | Impact on communication and navigation signals of marine species may also cause chronic stress. The density of water means that sound propagates much further and faster in water than in air |
| – | Thermal pollution | Heated industrial effluents; increasing sea surface temperature (global warming) | Heat causes oxygen depletion resulting in changes in species distribution and metabolism, possible breakdown of symbiosis (e.g. coral bleaching). Heat may also increase the toxicity of chemical contaminants noting that tropical species tend to live closer to their upper temperature thresholds than temperate species but some species adapt |
This text and table are adapted from “Marine Pollution in Context” In: Reichelt-Brushett, A. (eds) “Marine Pollution – Monitoring, Management and Mitigation” 2023, by Amanda Reichelt-Brushett, which is licensed under CC BY 4.0.
Multiple stressors
Marine environments are rarely exposed to a single stressor, but rather experience a complex mix of many stressors. These stressors may be contaminants, such nutrients, chemicals, plastics as well as carbon dioxide, or they may be other stressors, such as invasive species, built infrastructure, aquaculture or fisheries, or climatic changes which themselves can contribute to contaminant stress, for example, nutrient loading is a well-known impact from aquaculture activities. All these stressors are ubiquitous in marine environments worldwide and have the potential to interact and have very different impacts compared to if they occurred singularly.

‘Pipe with Sewage’ by Joseph Russo is used under a Pexels License
Understanding how and when stressors interact is critical for predicting their effects and therefore establishing safe and realistic guidelines to protect the environment. The consequences of stressor interactions are complex and pose great challenges for researchers, practitioners and decision-makers.
Multiple stressor interactions
When more than one stressor occurs in an environment, they may or may not interact. If the effects of a certain stressor occur independently of any other stressor in the environment, then we consider that the stressors are not interacting (no interaction; Figure 1). This is defined as an additive (or cumulative) multiple stressor model where the overall total effects on a response variable are the sum of the single-stressor effects.
Conversely, the stressors may affect the biological system(s) in ways that are dependent on each other or are interacting. Therefore, the overall or combined effects of two or more stressors are different from the sum of the single-stressor effects. Interacting stressors are considered as either synergistic or antagonistic, which are defined as (Figure 1):
- Synergistic Interactions—the combined effects are greater than expected based on individual effects.
- Antagonistic Interactions—the combined effects are less than expected based on individual effects.

Examples of multiple stressors
Wastewater treatment plants and stormwater drains that discharge into coastal marine waters create multiple stressor conditions since they are sources of both nutrients and trace metals and metalloids. These contaminants have different modes of action, often leading to different types of ecological impacts. When acting separately, moderate levels of nutrients may cause an increase in a particular biological or ecological response (e.g. population growth or primary productivity) compared to control areas (e.g. Svensson et al. 2007), while trace metals may cause a relative decrease in these responses (Johnston and Roberts 2009; Mayer-Pinto et al. 2010). However, when these stressors occur simultaneously, they are likely to interact and can potentially result in no overall net effect on biological or ecological responses in the receiving environment (O’Brien et al. 2019).
Another multiple stressor situation occurs when built infrastructure (e.g. marinas, groynes or piers) is in proximity to toxic chemicals in the water column. Built infrastructure on its own can cause a significant negative effect on the diversity (i.e. number of species and abundance) of marine organisms (e.g. microbes, plankton, epibiota, and infauna) via loss or fragmentation of habitats (Bulleri and Chapman 2010; Dafforn et al. 2015; Bishop et al. 2017). This may be further exacerbated by toxic chemicals (e.g. metals; industrial wastes and agricultural runoff; McGee et al. 1995), with the overall effect of these stressors being potentially greater than if the two stressors occurred separately (a synergistic effect).
This text, Figure 1 and its associated caption is from “Multiple Stressors” In: Reichelt-Brushett, A. (eds) “Marine Pollution – Monitoring, Management and Mitigation” 2023, by Allyson L. O’Brien, Katherine Dafforn, Anthony Chariton, Laura Airoldi, Ralf B. Schäfer, Mariana Mayer-Pinto, which is licensed under CC BY 4.0
Activity: Test your Knowledge
Test your knowledge in the quiz below:
Activity Text Version
Activity: Test your Knowledge
This exercise invites readers to answer questions to test their knowledge, based on the Contaminant Behaviour, Exposure, Uptake and Impact of Marine Pollution information above. Questions and answers are listed below.
Question 1
This question invites readers to fill-in 2 different terms to complete the definitions.
Answers to question 1
Bioconcentration is the process where chemicals are taken up by an organism directly from the water or surrounding environment (e.g. sediment) and accumulate in concentrations higher than the surrounding environment, where as, bioaccumulation is where chemicals are taken up by an organism both from the surrounding environment and through dietary accumulation.
Question 2
Select all correct statements. Select all that apply from:
- Biomagnification is the process whereby tissue concentrations of bioaccumulated compounds increase with each trophic level.
- Bioavailability refers to the totality of a contaminant that is present in the water column and media such as sediment which surrounds an organism
- Examples of substances that biomagnify include DDT, Methylmercury, halogenated hydrocarbons
- A change in pH, such as a decrease that we are seeing as a result of increased carbon dioxide, can affect the solubility and therefore bioavailability of contaminants to biota.
Answers to question 2
- Biomagnification is the process whereby tissue concentrations of bioaccumulated compounds increase with each trophic level.
- Examples of substances that biomagnify include DDT, Methylmercury, halogenated hydrocarbons
- A change in pH, such as a decrease that we are seeing as a result of increased carbon dioxide, can affect the solubility and therefore bioavailability of contaminants to biota.
Question 3
Select each statement that is correct. Select all that apply from:
- Different factors can influence the toxicity of a substance making them either more or less toxic to an individual. These can include: temperature, previous exposure to that pollutant, life history stage and the duration of exposure.
- If an organism is exposed to chemical x and chemical y individually, they do not show any deleterious response, however if exposed to both chemical x and y together, they see negative impacts. This is an example of a synergistic effect.
- If an organism is exposed to chemical x and chemical y individually, they do not show any deleterious response, however if exposed to both chemical x and y together, they see negative impacts. This is an example of a antagonistic or additive effect.
- An organism being exposed to pollution as well as increased temperature and acidity as a result of climate change is an example of multiple stressors impacting an organism
Answers to question 3
- Different factors can influence the toxicity of a substance making them either more or less toxic to an individual. These can include: temperature, previous exposure to that pollutant, life history stage and the duration of exposure.
- If an organism is exposed to chemical x and chemical y individually, they do not show any deleterious response, however if exposed to both chemical x and y together, they see negative impacts. This is an example of a synergistic effect.
- An organism being exposed to pollution as well as increased temperature and acidity as a result of climate change is an example of multiple stressors impacting an organism
Question 4
This question invites readers to fill-in 3 different terms to complete the definitions.
Answers to question 4
An organism is exposed to species x, y and z individually and in different combinations. Effects are given a number between 0 & 100 where zero is no effect and 100 is serious biological effect. When the organism was exposed to chemical x and y and z individually, there was no biological response for x (0), a 10 for y, and a biological response of 20 for z. When chemical y and z were exposed together, there was a biological response of 30. This is known as a/an additive effect. When chemical y and z were exposed together, there was a biological response of 5. This is known as a/an antagonistic effect. When all three chemicals were combined, the biological response was 50. This is known as a/an synergistic effect.
End Activity Text Version
References
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Bulleri, F., & Chapman, M. G. (2010). The introduction of coastal infrastructure as a driver of change in marine environments. Journal of Applied Ecology, 47(1), 26-35. https://doi.org/10.1111/j.1365-2664.2009.01751.x
Chapman, P. M., McDonald, B. G., Kickham, P. E., & McKinnon, S. (2006). Global geographic differences in marine metals toxicity. Marine pollution bulletin, 52(9), 1081-1084. https://doi.org/10.1016/j.marpolbul.2006.05.004
Chariton, A. A., Roach, A. C., Simpson, S. L., & Batley, G. E. (2010). Influence of the choice of physical and chemistry variables on interpreting patterns of sediment contaminants and their relationships with estuarine macrobenthic communities. Marine and Freshwater Research, 61(10), 1109-1122. https://doi.org/10.1071/MF09263
Dafforn, K. A., Glasby, T. M., Airoldi, L., Rivero, N. K., Mayer-Pinto, M., & Johnston, E. L. (2015). Marine urbanization: an ecological framework for designing multifunctional artificial structures. Frontiers in Ecology and the Environment, 13(2), 82-90. https://doi.org/10.1890/140050
de Almeida Rodrigues, P., Ferrari, R. G., Kato, L. S., Hauser-Davis, R. A., & Conte-Junior, C. A. (2022). A systematic review on metal dynamics and marine toxicity risk assessment using crustaceans as bioindicators. Biological Trace Element Research, 200(2), 881-903. https://doi.org/10.1007/s12011-021-02685-3
Hall, L. W., & Anderson, R. D. (1995). The influence of salinity on the toxicity of various classes of chemicals to aquatic biota. Critical Reviews in Toxicology, 25(4), 281-346. https://doi.org/10.3109/10408449509021613
Johnston, E. L., & Roberts, D. A. (2009). Contaminants reduce the richness and evenness of marine communities: a review and meta-analysis. Environmental pollution, 157(6), 1745-1752. https://doi.org/10.1016/j.envpol.2009.02.017
McGee, B. L., Schlekat, C. E., Boward, D. M., & Wade, T. L. (1995). Sediment contamination and biological effects in a Chesapeake Bay marina. Ecotoxicology, 4(1), 39-59. https://doi.org/10.1007/BF00350649
Mayer-Pinto, M., Underwood, A. J., Tolhurst, T., & Coleman, R. A. (2010). Effects of metals on aquatic assemblages: what do we really know?. Journal of Experimental Marine Biology and Ecology, 391(1-2), 1-9. https://doi.org/10.1016/j.jembe.2010.06.013
O’Brien, A. L., Dafforn, K. A., Chariton, A. A., Johnston, E. L., & Mayer-Pinto, M. (2019). After decades of stressor research in urban estuarine ecosystems the focus is still on single stressors: a systematic literature review and meta-analysis. Science of the Total Environment, 684, 753-764. https://doi.org/10.1016/j.scitotenv.2019.02.131
Svensson, C. J., Pavia, H., & Toth, G. B. (2007). Do plant density, nutrient availability, and herbivore grazing interact to affect phlorotannin plasticity in the brown seaweed Ascophyllum nodosum. Marine Biology, 151(6), 2177-2181. https://doi.org/10.1007/s00227-007-0649-5