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Important groups of chemicals
metals and metalloids
polycyclic aromatic hydrocarbons
organo halogenated compounds
pesticides
other
Chemical properties of polyhalogenated compounds
• Extremely low water solubility
• High lipophilicity
• High affinity to soil organic matter
• High affinity to fatty tissues
• High persistency
Note: PFAS (polyfluorinated compounds) more water soluble, not fat-
accumulating, but extremely persistent
Toxicological properties of polyhalogenated compounds
• Strong bioaccumulation
• Strong food chain accumulation (biomagnification)
• Low acute toxicity (but e.g., acne by dioxins)
• Immunotoxicity (PCBs)
• Estrogenic activity (PCBs, dioxins, DDT)
• Carcinogenicity (dioxins)
• Effects on vitamin A status (PCBs)
• Effects on vitamin K/blood coagulation (PCBs, dioxins)
• Teratogenic effects (dioxins)
sources of PAH
crude oil and petrol
exhaust of motorized engines
burning of organic material
industrial sources
sources of dioxins and dibenzofurans
1. Accidents in industries using
chlorinated phenols, e.g., Seveso 1976
2. Impurities (by-products) in chlorinated
pesticides, e.g., 2,4,5-T, Agent Orange
3. Impurities of PCBs
4. Burning of waste materials containing
chlorinated products or chlorine salts
(PVC, pesticide residues etc.)
5. Burning of (salt) peat
6. Effluents of paper mills (chlorine used to bleach paper
important pesticides
1. Chlorinated pesticides
2. Organophosphates
3. Carbamates
4. Pyrethroids
5. Neonicotinoids
6. Phenoxy herbicides
7. Triazines
8. Triazole fungicides
9. Organotin compounds
Degradation of chemicals
1. Decomposition (mainly used in ecology: leaf litter and other
organic material)
2. Photodegradation: by light (visible light, UV)
3. Thermal degradation: by high temperature
4. Chemical degradation: under influence of chemical activity
5. Biodegradation: by the action of microorganisms
6. Biotransformation: inside organisms (to facilitate excretion)
by: 1. Mineralisation à CO2, H 2O, etc.
2. Transformation à metabolites, intermediates
Physical aspects of bioavailability in soil
• Possibilities to penetrate soil
• Rooting depth of plants
• Living layer of soil animals or microorganisms
• Distribution of pollutant over soil solid phase (soil particles) and pore water
• Distribution of pollutant over small and large soil pores
*These factors will determine whether an organism will be exposed to a pollutant or not
Exposure scenario + things to consider
subpopulation
exposure pathway
concentrations and amounts
time unit, allometric unit, temporal scale & endpoint
Mechanisms to reduce toxicity of chemicals
1. Remove chemicals from body
• Passive or active excretion
2. Convert chemical into less toxic form
• Biotransformation, may also facilitate excretion
3. Store chemical in inert form
• Storage of metals in granules or bones
• Storage of organic chemicals in lipids
general principle of biotransformation
chemical is converted into polar metabolite
molecular weight is increased by conjugation, increasing solubility by transferases
excretion is stimulated
general principles of toxicity
routes of exposure
phases in toxic response
endpoints (structural or functional)
classification of toxic response
Response to a toxicant depends on
type of toxicant & testing organism
response type & endpoint
exposure duration & environmental conditions
to consider for ecotoxicity testing
representative of ecosystem to protect
representative of the relevant responses
uniformity
financial and ethical considerations
Properties of dioxinlike compounds
Very persistent against breakdown
Bioaccumulative (hydrophobic)
Same mode of action
Same clinical symptoms
Toxicity is additive: can be summed together
pesticides MoA
organochlorine pesticides; mess with action potential
organophosphate esters and carbamatic esters; Ah enzym blockation
pyrethroids; negative after-potential
neonicotinoids; activate AhR
Endocrine disrupting compounds
thyroid hormone disrupting compounds
steroidogenesis disruption
estrogen receptor agonists
advantages of biomarkers
Integrated measurement of exposure (in space and time)
Provide indication of bioavailability
Provide some indication of potential risk
May provide some indication of route of exposure
Can be applied to feral organisms exposed in situ
• i.e. not artificially exposed
problems with biomarker and interpretation
Effect of confounding factors (e.g. temperature, soil moisture, reproductive cycle, life stage, etc.)
Statistical vs. ecological relevance of measured response (what is normal level of response?)
Meaning of biomarker response for higher levels of biological organization (individual, population, community
Specificity vs. non-specificity of biomarker response
biomarker examples
biotransformation enzymes
reproductive and endocrine parameters
neuromuscular parameters
genotoxic parameters
main assumptions in ecotoxico R.A.
1. Functioning of the system is protected when structure (= species) is protected
2. Sensitivity of ecosystem is determined by its most sensitive species
3. Sensitivity of species in ecosystem can be described by log-logistic or other statistical distribution
4. Maximum acceptable risk (MAR) corresponds to protection of 95% of the species
5. Serious danger (SD) corresponds to protection of 50% of the species
restrictions to SSD R.A.
only applicable to toxicity data of same type
8 values needed
test organisms should be representative
only applicable to species
steps to make a RE framework
identify stress and ecosystem process
identify response traits to stress
identify trophic effect and response traits
identify effect traits that determine process
analyze linkages between response and effect traits
structural equation modelling
problems with RE framework
multitrophic environment effects
increasing number of trophic levels
feedback ecosystem to trophic levels
mutualistic interactions underlying effects
pop exposure
natural origin
intentional poisoning
disaster
illegal activities
background levels
advantage and disadvantages of effect-based monitoring
acounts for bioavailability and mixture effects
metabolites and unkown substances included
cost-effective
- no regulatory threshold
- low substance specificity
- no chronic effect included
- no biomagnification uncluded