Dietary Toxicity Thresholds and Ecological Risks for Birds and Mammals Based on Species Sensitivity Distributions.

Species sensitivity distributions (SSDs) are commonly used in regulatory procedures and ecological risk assessments. Yet, most toxicity threshold and risk assessment studies are based on invertebrates and fish. In the present study, no observed effect concentrations (NOECs) specific to birds and mammals were used to derive SSDs and corresponding hazardous concentrations for 5% of the species (HC5 values). This was done for 41 individual substances as well as for subsets of substances aggregated based on their toxic Mode of Action (MoA). In addition, potential differences in SSD parameters (mean and standard deviation) were investigated in relation to MoA and end point (growth, reproduction, and survival). The means of neurotoxic and respirotoxic compounds were significantly lower than those of narcotics, whereas no differences were found between end points. The standard deviations of the SSDs were similar across MoA's and end points. Finally, the SSDs obtained were used in a case study by calculating Ecological Risks (ER) and multisubstance Potentially Affected Fractions of species (msPAF) based on 19 chemicals in 10 Northwestern European estuaries and coastal areas. The assessment showed that the risks were all below 2.6 × 10-2. However, the calculated risks underestimate the actual risks of chemicals in these areas because the potential impacts of substances that were not measured in the field or for which no SSD was available were not included in the risk assessment. The SSDs obtained can be used in regulatory procedures and for assessing the impacts of contaminants on birds and mammals from fish contaminants monitoring programs.

Modeling the impacts of multiple environmental stress factors on estuarine copepod populations.

Many studies have focused on natural stress factors that shape the spatial and temporal distribution of calanoid copepods, but bioassays have shown that copepods are also sensitive to a broad range of contaminants. Although both anthropogenic and natural stress factors are obviously at play in natural copepod communities, most studies consider only one or the other. In the present investigation, we modeled the combined impact of both anthropogenic and natural stress factors on copepod populations. The model was applied to estimate Eurytemora affinis densities in the contaminated Scheldt estuary and the relatively uncontaminated Darß-Zingst estuary in relation to temperature, salinity, chlorophyll a, and sediment concentrations of cadmium, copper, and zinc. The results indicated that temperature was largely responsible for seasonal fluctuations of E. affinis densities. Our model results further suggested that exposure to zinc and copper was largely responsible for the reduced population densities in the contaminated estuary. The model provides a consistent framework for integrating and quantifying the impacts of multiple anthropogenic and natural stress factors on copepod populations. It facilitates the extrapolation of laboratory experiments to ecologically relevant end points pertaining to population viability.

Modelling the impact of toxic and disturbance stress on white-tailed eagle (Haliaeetus albicilla) populations.

Several studies have related breeding success and survival of sea eagles to toxic or non-toxic stress separately. In the present investigation, we analysed single and combined impacts of both toxic and disturbance stress on populations of white-tailed eagle (Haliaeetus albicilla), using an analytical single-species model. Chemical and eco(toxico)logical data reported from laboratory and field studies were used to parameterise and validate the model. The model was applied to assess the impact of ∑PCB, DDE and disturbance stress on the white-tailed eagle population in The Netherlands. Disturbance stress was incorporated through a 1.6% reduction in survival and a 10-50% reduction in reproduction. ∑PCB contamination from 1950 up to 1987 was found to be too high to allow the return of white-tailed eagle as a breeding species in that period. ∑PCB and population trends simulated for 2006-2050 suggest that future population growth is still reduced. Disturbance stress resulted in a reduced population development. The combination of both toxic and disturbance stress varied from a slower population development to a catastrophical reduction in population size, where the main cause was attributed to the reduction in reproduction of 50%. Application of the model was restricted by the current lack of quantitative dose-response relationships between non-toxic stress and survival and reproduction. Nevertheless, the model provides a first step towards integrating and quantifying the impacts of multiple stressors on white-tailed eagle populations.

Modeling bioaccumulation and biomagnification of nonylphenol and its ethoxylates in estuarine-marine food chains.

There are several studies on bioaccumulation and biomagnification of nonylphenol (NP) and its ethoxylates (NPEOs), but their toxico-kinetic mechanisms remain unclear. In the present investigation, we explored the accumulation of NP and NPEOs in estuarine-marine food chains with a bioaccumulation model comprising five trophic levels. Using this model, we estimated uptake and elimination rate constants for NPEOs based on the organisms' weight and lipid content and the chemicals' Kow. Further, we calculated accumulation factors for NP and NPEOs, including biota-sediment accumulation factors (BSAF) and biomagnification factors (BMF), and compared these to independent field measurements collected in the Western Scheldt estuary in The Netherlands and field data reported in the literature. The estimated BSAF values for NP and total NPEOs were below 1 for all trophic levels. The estimated BMF values were around 1 for all trophic levels except for the highest level (carnivorous mammals and birds). For this trophic level, the estimated BMF value varied between 0.1 and 2.4, depending on the biotransformation capacity. For all trophic levels, except primary producers, the accumulation estimates that accounted for biotransformation of NPEOs into NP were closer to the field data than model estimates that did not include biotransformation, indicating that NP formation by biotransformation of NPEOs might occur in organisms.