Rare earth elements (REE) are in high demand due to their applications in the medical, green energy and high-tech industries. As a result, new REE mines are being developed with the potential of mobilizing REE and increasing their concentrations in the environment, including in landfills, wastewaters and natural waters. Unfortunately, the concentrations of trivalent REE cations are generally poorly predictive of biological effects, especially when attempting to understand the role of REE complexation within bioavailability models, such as the Biotic Ligand Model (BLM). We investigated the bioavailability of a representative REE, lanthanum (La), by measuring biouptake fluxes for Chlamydomonas reinhardtii. In the presence of a small amount (0.5 mg C L-1) of natural organic matter (NOM), for a calculated reduction in La3+ of >90%, La biouptake decreased between 43 and 87%. Furthermore, the concentration of dissolved organic carbon was not sufficient to predict the effect of NOM on La biouptake, with the effect varying greatly as a function of NOM origin. Eleven NOM samples were extensively characterised in order to relate NOM quality to its effect on biouptake. The most aromatic and allochthonous NOM had the greatest effect on reducing La biouptake. For example, for an NOM concentration of 10 mg C L-1, the most allochthonous NOM tested (Suwannee River Humic Acid, fluorescence index = 1.2) reduced La biouptake by 95% as compared to a reduction of 67% for the most autochthonous NOM (Cameroun River, fluorescence index = 1.9). The study is useful for improving our understanding of the important factors affecting REE bioavailability in natural systems.

In hypoxia, the initial response in vertebrates is hyperventilation, known as the Hypoxic Ventilatory Response (HVR), which is a physiological reflex that allows fish to maintain adequate oxygen uptake to meet metabolic demands. The severity of hypoxia in aquatic ecosystems is growing due to anthropogenic impacts. This is a concern with the recent evidence that metals can affect the ability of fishes to mount the HVR. As Rare Earth Elements (REEs), such as neodymium (Nd) increase in demand with the shift to a low-carbon, green economy, there is a critical need to understand their environmental consequences. Here, we investigate whether exposure to Nd will blunt the HVR in fathead minnows (Pimephales promelas). Fathead minnows were exposed to 93 ± 7.9 µg/L Nd for 48-h and subjected to 40

Remote sensing can provide an alternative solution to quantify Dissolved Organic Carbon (DOC) in inland waters. Sensors embedded on Unmanned Aerial Vehicles (UAV) and satellites that can capture the DOC have already shown good relationships between DOC and the Colored Dissolved Organic Matter absorption (aCDOM.) coefficients in specific spectral regions. However, since the signal recorded by the sensors is reflectance-based, DOC estimates accuracy decreases when inverting the aCDOM. coefficients to reflectance. Thus, the main objective is to study the potential of a UAV-borne hyperspectral camera to retrieve the DOC in inland waters and to develop reflectance-based models using UAV and satellite (Landsat-8 OLI and Sentinel-2 MSI) data. Ensemble based systems (EBS) were favored in this study. The EBSUAV calibration results showed that six spectral regions (543.5, 564.5, 580.5, 609.5, 660, and 684 nm) are sensitive to DOC in waters. The EBSUAV test results showed a good concordance between measured and estimated DOC with an R-2 = Nash-criterion (NASH) = 0.86, and RMSE (Root Mean Squares Error) = 0.68 mg C/L. The EBSSAT test results also showed a strong concordance between measured and estimated DOC with R-2 = NASH = 0.92 and RMSE = 0.74 mg C/L. The spatial distribution of DOC estimates showed no dependency to other optically active elements. Nevertheless, estimates were sensitive to haze and sun glint.

The use of persistence, bioaccumulation, and toxicity (PBT) criteria to identify chemical substances of high environmental concern has been in use since the early 1970s. This article is protected by copyright. All rights reserved. © 2022 SETAC.

The demand for rare earth elements (REEs) is growing and as a result, environmental exposure is a concern. The objective of this research was to evaluate the acute toxicity of Tm to Hyalella azteca and to understand the potential for toxicity modification by dissolved organic matter (DOM) and the cations Ca2+, Mg2+ and Na+. Standard methods were followed for 96 h static exposures in a medium with a hardness of 60 mg CaCO3/L, pH of 7.3 at 23 °C. H. azteca neonates (2–9 d of age) were used and in unmodified media the LC50 concentration was 3.4 µM [95% CI 2.9–3.9 µM; 573 µg/L (482–663)] based on measured dissolved concentrations at the end of the test. Tests done with different concentrations of Ca (0.25, 0.5 and 1.5 mM) did not show consistent trends and there was no clear evidence of a protective effect from Ca. Variations in Na (0.26, 0.5 and 1.6 mM) resulted in no significant changes in toxicity. Similarly, Mg (0.07, 0.14 and 0.4 mM) did not result in significant changes in LC50 values, except for a reduction in toxicity for measured total Tm at the lowest Mg concentration. Our results indicate that Tm toxicity is not influenced by cationic competition (Ca, Na and Mg). Dissolved organic matter (sourced from Luther Marsh ON) offered significant protection against Tm toxicity. Addition of 9 mg DOC/L resulted in significantly increased LC50 values. This study contributes toward understanding the toxicity of Tm and the importance of considering dissolved organic matter in estimating the potential for environmental risk of REEs.

The potential for Ni toxicity in seawater is of concern because of mining and processing activities in coastal regions. Determining Ni speciation is vital to understanding and predicting Ni toxicity and for bioavailability-based nickel risk assessment. The goal of this study was to characterize the complexation of Ni in relation to toxicity using embryological development of purple sea urchin (S. purpuratus). It was predicted that free ion [Ni2+] would be a better predictor of toxicity than total dissolved Ni concentrations (NiD). Synthetic ligands with known logKf values (Ethylenediaminetetraacetic acid (EDTA), Nitrilotriacetic acid (NTA), tryptophan (TRP), glutamic acid (GA), histidine (HD), and citric acid (CA)) were used to test the assumptions of the biotic ligand model (BLM) for Ni in seawater. [NiD] was measured by graphite furnace atomic absorption spectroscopy (GFAAS) and Ni2+ was first quantified using the ion-exchange technique (IET) and then concentrations were measured by GFAAS; [Ni2+] was also estimated using aquatic geochemistry modelling software (Visual Minteq). The mean EC50 values for [NiD] in unmodified artificial seawater control was 3.6 µM (95% CI 3.0–4.5) [211 µg/L 95% CI 176–264] and the addition of ligands provided protection, up to 6.5-fold higher [NiD] EC50 for EDTA. Compared to the control, measured EC50 values based on total dissolved nickel were higher in the presence of ligands. As predicted by BLM theory, [Ni2+] was a better predictor of Ni toxicity with 17% variability in EDTA and CA media while there was 72% variability in the prediction of Ni toxicity with total dissolved Ni. The results of this research provide support for the application of BLM- based prediction models for estimating Ni impacts in seawater.

Dissolved organic carbon (DOC) is known to ameliorate the toxicity of the trace metal nickel (Ni) to aquatic animals. In theory, this effect is mediated by the capacity of DOC to bind Ni, rendering it less bioavailable, with the resulting reduction in accumulation limiting toxicological effects. However, there is a lack of experimental data examining Ni accumulation in marine settings with natural sources of DOC. In the current study, radiolabelled Ni was used to examine the time- and concentration-dependence of Ni accumulation, using naturally sourced DOC, on developing larvae of the sea urchin Strongylocentrotus purpuratus. Contrary to prediction, the two tested natural DOC samples (collected from the eastern United States, DOC 2 (Seaview park, Rhode Island (SVP)) and DOC 7 (Aubudon Coastal Center, Connecticut)) which had previously been shown to protect against Ni toxicity, did not limit accumulation. The control (artificial seawater with no added DOC), and the DOC 2 sample could mostly be described as having saturable Ni uptake, whereas Ni uptake in the presence of DOC 7 was mostly linear. These data provide evidence that DOC modifies the bioavailability of Ni, through either indirect effects (e.g. membrane permeability) or by the absorption of DOC-Ni complexes. There was some evidence for regulation of Ni accumulation in later-stage embryos (96-h) where the bioconcentration factor for Ni declined with increasing Ni exposure concentration. These data have implications for predictive modelling approaches that rely on known relationships between Ni speciation, bioavailability and bioreactivity, by suggesting that these relationships may not hold for natural marine DOC samples in the developing sea urchin model system.

The primary goal of the present study is to provide a broad view of best practices for evaluating bioavailability models for metals for use in the protection of aquatic life. We describe the state of the science regarding 1) the evaluation and selection of ecotoxicity data, 2) the selection of bioavailability models for use in normalization, and 3) subsequent application of bioavailability models. Although many examples of normalization steps exist worldwide, a scheme is proposed to evaluate and select a model that takes account of its representativeness (water chemistry and taxonomic coverage of the ecotoxicity data set) and validation performance. Important considerations for a suitable model are the quantity of inputs needed, accuracy, and ease of use, all of which are needed to set protective values for aquatic life and to use these values to evaluate potential risks to organisms in receiving waters. Although the end results of different model application approaches may be broadly similar, the differences in these application frameworks ultimately come down to a series of trade-offs between who needs to collect the data and use the bioavailability model, the different requirements of spatial scales involved (e.g., regional vs site-specific values), and model predictiveness and protectiveness. Ultimately, understanding the limits and consequences of these trade-offs allows for selection of the most appropriate model and application framework to best provide the intended levels of aquatic life protection. Environ Toxicol Chem 2019;39:118-130. © 2019 SETAC.

Cadmium is an endocrine disruptor and inhibits corticosteroid production, but the mechanisms are far from clear. We tested the hypothesis that sublethal exposure to environmentally realistic levels of cadmium impairs cortisol production by disrupting the melanocortin 2 receptor (MC2R) signaling in rainbow trout (Oncorhynchus mykiss). Fish were exposed to sublethal concentrations of cadmium (0.75 or 2.0 mu g/L) in a flow-through system for 7 d and subjected to an acute secondary stressor to evoke a cortisol response. Cadmium exposure for 7 d did not affect plasma cortisol concentrations, but head kidney mc2r mRNA levels were higher than in control fish. The cortisol stress performance to a secondary-stressor was attenuated in the cadmium groups, and this corresponded with transient reduction in transcript abundance of mc2r and the gene encoding its accessory protein MRAP1 but not MRAP2 in the head kidney. Furthermore, in vivo cadmium exposure attenuated the adrenocorticotropic hormone (ACTH)-, but not 8-br-cAMP-stimulated cortisol production in head kidney slices ex vivo. This corresponded with reduced transcript abundance of mc2r and mrap1, but not mrap2 in these tissue slices. Also, reporter assays with CHO cells transiently transfected with rainbow trout mc2r and zebrafish mrap1 revealed a dose-independent inhibition in ACTH-stimulated luciferase activity by cadmium. Collectively, waterborne exposure to environmentally realistic concentration of cadmium compromises the stressor-induced cortisol response, and a mode of action involves the disruption of MC2R signaling in rainbow trout.

Nickel (Ni) emissions resulting from production and transportation raise concerns about the impact of Ni exposure to marine ecosystems. Ni bioavailability models are established for FW systems, but the influence of chemical parameters (e.g. dissolved organic carbon (DOC)) on Ni toxicity within marine systems is less well understood. To examine the effects of DOC concentration and composition on Ni toxicity, acute toxicity tests were conducted on early life-stages of blue mussels (Mytilus edulis) and sea urchin embryos (Strongylocentrotus purpuratus) in full strength sea water (32 ppt). Nine different field collected samples of water with varying concentration (up to 4.5 mg C/L) and composition of DOC were collected from the east coast of the United States. Organic matter compositional analysis included molecular fluorescence and absorbance spectroscopy. The different DOC sources had different protective effects against embryo toxicity. The control (no DOC) Ni 48 h-EC50 for Mytilus embryos was 133 mu g/L (95% confidence interval (C.I.) of 123-144 mu g/L), while Strongylocentrotus embryos displayed control 96-h EC50 values of 207 mu g/L (167-247 mu g/L). The most significantly protective sample had high humic acid concentrations (as determined from fluorescence spectroscopy), which yielded an EC50 of 195 mu g/L (169-222 mu g/L) for Mytilus, and an EC50 of 394 mu g/L (369-419 mu g/L) for S. purpuratus. Among all samples, protection was related to both DOC quantity and quality, with fluorescence-resolved humic and fulvic acid concentrations showing the strongest correlations with protection for both species. These data suggest that DOC is protective against Ni toxicity in M. edulis and S. purpuratus, and that accounting for a DOC quality factor will improve predictive toxicity models such as the biotic ligand model.

Speciation of copper in marine systems strongly influences the ability of copper to cause toxicity. Natural organic matter (NOM) contains many binding sites which provides a protective effect on copper toxicity. The purpose of this study was to characterize copper binding with NOM using fluorescence quenching techniques. Fluorescence quenching of NOM with copper was performed on nine sea water samples. The resulting stability constants and binding capacities were consistent with literature values of marine NOM, showing strong binding with \(\log K\) values from 7.64 to 10.2 and binding capacities ranging from 15 to 3110 nmol mg \({\text {C}}^{-1}.\) Free copper concentrations estimated at total dissolved copper concentrations corresponding to previously published rotifer effect concentrations, in the same nine samples, were statistically the same as the range of free copper calculated for the effect concentration in NOM-free artificial seawater. These data confirms the applicability of fluorescence spectroscopy techniques for NOM and copper speciation characterization in sea water and demonstrates that such measured speciation is consistent with the chemical principles underlying the biotic ligand model approach for bioavailability-based metals risk assessment.

The emergence of omics approaches in environmental research has enhanced our understanding of the mechanisms underlying toxicity; however, extrapolation from molecular effects to whole-organism and population level outcomes remains a considerable challenge. Using environmentally relevant, sublethal, concentrations of two metals (Cu and Ni), both singly and in binary mixtures, we integrated data from traditional chronic, partial life-cycle toxicity testing and metabolomics to generate a statistical model that was predictive of reproductive impairment in a Daphnia pulex-pulicaria hybrid that was isolated from an historically metal-stressed lake. Furthermore, we determined that the metabolic profiles of organisms exposed in a separate acute assay were also predictive of impaired reproduction following metal exposure. Thus we were able to directly associate molecular profiles to a key population response - reproduction, a key step towards improving environmental risk assessment and management.

Environmental context Organic matter dissolved in water can mitigate toxic effects of copper, which should be taken into account when estimating risks of copper pollution. The composition of this organic matter, however, can vary widely, and these variations might also need to be taken into account. This work addresses the question of organic matter quality and demonstrates that only the amount and not the source influences copper toxicity – good news for risk analysis because it simplifies predictions of the effects of copper in specific receiving waters. Abstract The toxicity of copper in marine systems is dependent on its speciation and bioavailability. Dissolved organic matter (DOM) can complex copper, resulting in decreased bioavailability and hence decreased toxicity. The purpose of this study was to measure acute copper LC50 values (concentration lethal to 50% of the organisms) in natural marine waters in a sensitive organism, and identify the relationships between DOM quality and copper toxicity and speciation. Static acute copper toxicity tests (48-h LC50) were performed using the euryhaline rotifer Brachionus plicatilis. Ion-selective electrode measurements of free copper were performed at the LC50 concentrations to determine the influence of DOM source on copper speciation. LC50 values ranged from 333 to 980nM (21.1 to 62.3µgL–1) with DOC concentrations ranging from 0.55 to 7.57mgCL–1. DOC was found to be protective (R2 = 0.72, P = 0.016); however, the degree of protection decreased as DOC increased. This suggests salt-induced colloid formation could be occurring, resulting in a decrease of binding sites available to complex free copper. Free copper remained fairly constant between each sample site, with an average pCu of 10.14. Overall, this study is consistent with other studies that suggest free copper is the best species for predicting toxicity. Additionally, no significant correlation between DOM source and copper toxicity was observed as compared with total DOC concentration and copper toxicity, suggesting that DOM quality does not need to be taken into account for copper toxicity modelling in salt water.

The recovery of lakes from severe, historical acid and metal pollution requires that colonists of extirpated species arrive, survive and subsequently thrive. We employed 40 year records from weekly to monthly crustacean zooplankton samples from Middle and Clearwater lakes near Sudbury, Canada, to identify the main mechanistic bottlenecks in this recovery process. While both lakes now have circum-neutral pH, acidity decreased more rapidly in Middle Lake because of past liming interventions, while Clearwater Lake, being larger and supporting more housing, likely receives more zooplankton colonists than Middle Lake. Community richness increased much faster in Middle Lake than in Clearwater Lake, at 1.6 vs 0.9 species decade(-1), respectively. Richness has recovered in Middle Lake, when assessed against a target of 9-16 species collection(-1) determined from regional reference lakes, but it has not yet recovered in Clearwater Lake. Species accumulation curves and a metric of annual persistence show that this difference is a product not of greater rates of species introduction into Middle Lake, but rather to their greater annual persistence once introduced. Greater annual persistence was associated with better habitat quality (i.e., lower acid and metal toxicity) in Middle Lake, particularly early in the record, and lower planktivore abundance, more recently. These results support a growing consensus that ecological recovery of zooplankton from acidification and metal pollution does not depend strongly on propagule introduction rates which are adequate, but rather on propagule persistence, in lake-rich, suburban landscapes such as those near Sudbury.

Reductions in atmospheric emissions from the metal smelters in Sudbury, Canada, produced major improvements in acid and metal contamination of local lakes and indirectly increased dissolved organic carbon (DOC) concentrations. Metal toxicity, however, has remained a persistent problem for aquatic biota. Integrating high-throughput, nontargeted mass spectrometry metabolomics with conventional toxicological measures elucidated the mediating effects of dissolved organic matter (DOM) on the toxicity of Cu to Daphnia pulex-pulicaria, a hybrid isolated from these soft water lakes. Two generations of daphniids were exposed to Cu (0-20 μg/L) at increasing levels of natural DOM (0-4 mg DOC/L). Added DOM reduced Cu toxicity monotonically with median lethal concentration values increasing from 2.3 μg/L Cu without DOM to 22.7 μg/L Cu at 4 mg DOC/L. Reproductive output similarly benefited, increasing with DOM, yet falling with increases in Cu. Second generation reproduction was more impaired than the first generation. Dissolved organic matter had a greater influence than Cu on the metabolic status of the daphniids. Putative identification of metabolite peaks indicated that DOM elevation increased the metabolic energy status of the first generation animals, but this benefit was reduced in the second generation, although evidence of increased oxidative stress was detected. These results indicate that Sudbury's terrestrial ecosystems should be managed to increase aquatic DOM supply to enable daphniid colonists to both survive and foster stable populations.

The toxicological understanding of rare earth elements (REEs) in the aquatic environment is very limited but of increasing concern. The objective of this research is to compare the toxicological effect of the REE dysprosium to the freshwater invertebrates Daphnia pulex and Hyalella azteca and in the more sensitive organism, understand the toxicity modifying influence of Ca, Na, Mg, pH and dissolved organic matter (DOM). Standard methods (Environment Canada) were followed for testing and culture in media of intermediate hardness (60 mg CaCO3 mg/L) at pH 7.8 with Ca at 0.5, Na 0.5, Mg 0.125 (mM) and 23 °C. Acute toxicity tests were done with <24 h old neonates for 48 h in the case of D. pulex and with 2–9 days old offspring for 96 h tests with Hyalella. The potential protective effect of cationic competition was tested with Ca (0.5–2.0 mM), Na (0.5–2.0 mM) and Mg (0.125–0.5 mM). The effect of pH (6.5–8.0) and Suwannee River DOM complexation (at dissolved organic carbon (DOC) concentrations of 9 and 13 mg C/L) were evaluated. Dissolved Dy concentrations were lower than total (unfiltered) indicating precipitation, particularly at higher concentrations. Acute toxicity of Dy to H. azteca and D. pulex revealed Hyalella to be 1.4 times more sensitive than Daphnia. Additions of Ca and Na but not Mg provided significant protection against Dy toxicity to Hyalella. Similarly, low pH was associated with reduction in toxicity. Exposures which were pH buffered with and without MOPS were significantly different and indicated that MOPS enhanced Dy toxicity. DOM also mitigated Dy toxicity. Biotic ligand based parameters (Log K values) were calculated based on free ion relationships as determined by geochemical equilibrium modeling software (WHAM ver. 7.02). The log K value for Dy3+ toxicity to Hyalella was 7.75 while the protective influence of Ca and Na were 3.95 and 4.10, respectively. This study contributes data towards the development of site specific water quality guidelines and criteria for Dy and possibly REEs in general and offers insight into the complex bio-geochemical nature of this element.

This study investigates the effect of chronic Cd exposure on the ability to perform repeat swim challenges in brown trout (Salmo trutta) and lake whitefish (Coregonus clupeaformis). Fish were exposed to waterborne Cd (18nM) in moderately hard water (120mgL(-1) CaCO3) for 30 days. This level of exposure has been shown to cause sublethal physiological disruption and acclimation responses but no impairment of sustained swimming capacity (Ucrit) in single swim challenges. Swim trials were done over the course of the exposure and each one consisted of an initial swim to 85% of the Ucrit of control fish, a 30min recovery period and finally a second swim challenge to determine Ucrit. Plasma and tissue samples were collected before and after each of the swim periods. As expected from previous studies, Cd exposure resulted in significant accumulation of Cd in gills, liver and kidney but not in white muscle. Exposure also induced a loss of plasma Ca followed by subsequent recovery (in lake whitefish but not brown trout) with few mortalities (100% survival for lake whitefish and 93% for brown trout). Both control and exposed fish swam to 85% of the single swim Ucrit and no differences in performance were seen. The Ucrit of unexposed controls in the second swim challenges were not different from the single swim Ucrit. However, second swim performance was significantly reduced in Cd exposed fish, particularly after a week of exposure where 31% and 38% reductions were observed for brown trout and lake whitefish respectively. Swimming to 85% Ucrit resulted in metabolic expenditure with little recovery after 30min. Few differences were observed between control and Cd exposed fish with the exception of a reduction in resting white muscle ATP stores of Cd exposed fish after 1 week of exposure. The results show that chronic sublethal Cd exposure results in an impairment of swimming ability in repeat swim challenges but this impairment is generally not related to metabolic processes in white muscle.

Environmental context A Cu ion-selective electrode is potentially an excellent tool for cupric ion measurements in salt water, but it is prone to poor reproducibility. We show that dramatic improvements can be obtained by using a Cu ion-selective electrode and a one-point calibration method that corrects for electrode fouling. The method shows promise to be used to collect data on toxic cupric ion concentrations in saltwater environments. Abstract Free Cu is often used as an indicator for potential Cu toxicity. Free ionic Cu2+ was measured using a flow-through ion-selective electrode (ISE). Four different marine samples were collected from various locations and analysed during a fixed-pH Cu titration using an external standard calibration ISE method. Free cupric determinations in the range 10–12 to 10–7molL–1 were consistent with published literature but replicate measures showed up to four orders of magnitude variability. To improve reproducibility, an internal calibration method was developed. The new method was validated using artificial seawater with added tryptophan as the model ligand. The free Cu measured using the improved method showed the same trends as the external calibration data but reproducibility increased to an order of magnitude or better. The potential applicability of this new method was also highlighted in that it matches, in the environmentally and regulatory significant range of total Cu, with a fluorescence quenching method applied to one of the four samples. The ISE data do not agree with free ion concentrations estimated from anodic stripping voltammetry (ASV) though. This suggests that, at least for these samples, ASV responded to a larger fraction of total Cu than simply the inorganic complexes. Caution should be exercised when using ASV as a proxy for bioavailability because the trends in ASV-derived free Cu did not match the free Cu as estimated by ISE. This ability to more reliably measure free Cu is significant for predicting and measuring toxicity on Cu exposure.

This chapter describes approaches to environmental exposure assessments of metals and organic contaminants. The free ion activity model is an equilibrium-based geochemical speciation model to predict free metal ion concentrations, which are mainly associated with toxic effects. Biotic ligand models expand on this concept and predict the short-term binding of free ions to a biotic ligand, also based on equilibrium processes. Working either at equilibrium or in the kinetic phase, passive samplers are increasingly used to determine hydrophobic organic contaminants in the environment. Passive sampling techniques also exist for hydrophilic compounds and metals. The reserved concept of passive dosing can provide stable exposure concentrations in toxicity tests. Chemical monitoring in the context of the European Union Water Framework Directive or the Oslo–Paris Commission generates concentrations to be compared to toxicity-based environmental quality standards or assessment criteria. New analytical methods have been developed for the high quality trace analysis of organic compounds of emerging concern.