Increased tropospheric ozone (O₃) concentrations in boreal forests affect the emission of biogenic volatile organic compounds (BVOCs), which play crucial roles in biosphere-atmosphere feedbacks. Although it has been well documented that BVOC emissions are altered in response to elevated O₃, consequent effects on the carbon budget have been largely unexplored. Here, we studied the effects of elevated O₃ (80 nmol mol⁻¹) on diurnal variation of BVOC emissions and gas exchange of CO₂ from above- and belowground parts of Norway spruce (Picea abies) and Scots pine (Pinus sylvestris) and further investigated effects on the carbon budget. In spring, elevated O₃ decreased BVOC emissions and net photosynthesis rate (Pn) from above-ground parts of both species. As BVOC emissions have a causal relationship with dormancy recovery, O₃-induced decreases in BVOC emissions indicated the inhibition of dormancy recovery. Contrary to the spring results, in summer BVOC emissions from aboveground parts were increased in response to elevated O₃ in both species. Decreases in Pn indicated O₃ stress. O₃-induced monoterpene emissions from aboveground were the main volatile defense response. Elevated O₃ had little effect on BVOC emissions from belowground parts of either species in spring or summer. In spring, elevated O₃ decreased the proportion of carbon emitted as BVOCs relative to that assimilated by photosynthesis (the proportion of BVOC-C loss) at the soil-plant system levels in both species. In summer, elevated O₃ resulted in a net CO₂–C loss at the soil-plant system level of Scots pine. During this process, O₃-induced BVOC-C loss can represent a significant fraction of carbon exchange between the atmosphere and Scots pine. In Norway spruce, the effects of O₃ were less pronounced. The current results highlight the need for prediction of BVOC emissions and their contributions to the carbon budget in boreal forests under O₃ stress.

We investigated the tissue distribution, trophic transfer, and ecological risk of 13 trace elements in 26 East Asian finless porpoises (Neophocaena asiaeorientalis sunameri), an endangered species found in the Liaodong Bay and the north Yellow Sea. All the investigated trace elements were detected in the tissue and food web of the East Asian finless porpoises. The concentrations of the potentially toxic elements were 2.37 × 10⁻⁵ – 754 mg kg⁻¹ dry weight (dw) in stranded porpoises and 0.01–159 mg kg⁻¹ dw in their food web. Tissue-specific distribution of the trace elements generally ranked as: liver > kidney > heart > lung > muscle. Zn was the dominant contaminant in the five investigated tissues. Significant positive correlations were found between body length or age and some trace elements, especially Cd. Adults (≥2 years old) presented higher concentrations of most of the trace elements than juveniles (<2 years old). Sex-dependent distribution of the trace elements was insignificant except for Mn, Ni, and Zn in muscle and renal tissue. As, Cu, Mn, Ni, Pb, and V biodiluted across the East Asian finless porpoise food web while Zn biomagnified. However, Hg, Cd, Co, Cr, Se, and Sn did not exhibit apparent trophic transfer trends. Overall, ecological risk assessment of trace elements in East Asian finless porpoises suggested that greater attention should be given to Hg, As, Cd, and Se.

To evaluate pesticide regulatory standards in agricultural crops, we introduced a regulatory modeling framework that can flexibly evaluate a population’s aggregate exposure risk via maximum residue levels (MRLs) under good agricultural practice (GAP). Based on the structure of the aggregate exposure model and the nature of variable distributions, we optimized the framework to achieve a simplified mathematical expression based on lognormal variables including the lognormal sum approximation and lognormal product theorem. The proposed model was validated using Monte Carlo simulation, which demonstrates a good match for both head and tail ends of the distribution (e.g., the maximum error = 2.01% at the 99th percentile). In comparison with the point estimate approach (i.e., theoretical maximum daily intake, TMDI), the proposed model produced higher simulated daily intake (SDI) values based on empirical and precautionary assumptions. For example, the values at the 75th percentile of the SDI distributions simulated from the European Union (EU) MRLs of 13 common pesticides in 12 common crops were equal to the estimated TMDI values, and the SDI values at the 99th percentile were over 1.6-times the corresponding TMDI values. Furthermore, the model was refined by incorporating the lognormal distributions of biometric variables (i.e., food intake rate, processing factor, and body weight) and varying the unit-to-unit variability factor (VF) of the pesticide residues in crops. This ensures that our proposed model is flexible across a broad spectrum of pesticide residues. Overall, our results show that the SDI is significantly reduced, which may better reflect reality. In addition, using a point estimate or lognormal PF distribution is effective as risk assessments typically focus on the upper end of the distribution.

Cavity nesting bees are proficient and important pollinators that can augment or replace honey bee pollination services for some crops. Relatively little is known about specific pesticide concentrations present in cavity nesting insect reed matrices and associated potential risks to cavity nesting bees. Nesting substrates (Phragmites australis reeds in bundles) were deployed in an agriculturally intensive landscape to evaluate colonization and agrochemical exposure among cavity nesting pollinators over two consecutive field seasons. Composition of insect species colonizing reeds within nest bundles varied considerably; those placed near beef cattle feed yards were dominated by wasps (93% of the total number of individuals occupying reed nest bundles), whereas nest bundles deployed in cropland-dominated landscapes were colonized primarily by leaf cutter bees (71%). All nesting/brood matrices in reeds (mud, leaves, brood, pollen) contained agrochemicals. Mud used in brood chamber construction at feed yard sites contained 21 of 23 agrochemicals included in analysis and >70% of leaf substrate stored in reeds contained at least one agrochemical. Moxidectin was most frequently detected across all reed matrices from feed yard sites, and moxidectin concentrations in nonviable larvae were more than four times higher than those quantified in viable larvae. Agrochemical concentrations in leaf material and pollen were also quantified at levels that may have induced toxic effects among developing larvae. To our knowledge, this is the first study to characterize agrochemical concentrations in multiple reed matrices provisioned by cavity-nesting insects. Use of nest bundles revealed that cavity nesting pollinators in agriculturally intensive regions are exposed to agrochemicals during all life stages, at relatively high frequencies, and at potentially lethal concentrations. These results demonstrate the utility of nest bundles for characterizing risks to cavity nesting insects inhabiting agriculturally intensive regions.

Mecoprop-P (MCPP-P) is an auxin herbicide which has been used against dicotyledonous weed plants since the 1980s. While fate and monitoring data of MCPP-P in the aquatic environment revealing concentrations up to 103 μg/L in freshwaters are well documented, only very few toxicity data and no studies with dicotyledonous macrophytes have been published in open literature so far. To fill up this essential data gap, a microcosm study was conducted in order to test the sensitivity of nine dicotyledonous and one Ceratophyllales macrophyte species. The plant species were exposed to seven MCPP-P concentrations ranging from 8 to 512 μg/L for 21/22 days in one microcosm per concentration, and two further microcosms served as controls. Plant preparation was adapted to each species and endpoints were measured to calculate growth rates. Data were generated to obtain effect concentrations (ECX) which then were used to construct species sensitivity distribution curves (SSD). Eight species proved to be sensitive to MCPP-P in the tested concentration range with EC₅₀ values ranging from 46.9 μg/L for Ranunculus aquatilis to 656.4 μg/L MCPP-P for Ludwigia repens. Taking the EC₅₀ values of this study and published data for autotrophic organisms into account, a hazard concentration (HC₅) of 2.7 μg/L was derived from the SSD curve, while an SSD curve without dicotyledonous macrophytes resulted in an about 100 times higher HC₅ (360.8 μg/L MCCP-P). This confirms that a re-evaluation for old auxin herbicides by including dicotyledonous test species into the environmental risk assessment may be indicated. Furthermore, the use of MCPP-P in bitumen felts as protection against rooting by plants is not in the focus of any risk regulation so far. This application, however, can lead to high run-off concentrations that can enter surface waters easily, exceeding the new regulatory acceptable concentration values.

This study aims to investigate the adsorption behavior of cationic and anionic dyes of methylene blue (MB) and Congo red (CR) onto wet-torrefied Chlorella sp. microalgal biochar respectively, as an approach to generate a waste-derived and low-cost adsorbent. The wet-torrefied microalgal biochar possessed microporous properties with pore diameter less than 2 nm. The optimum adsorbent dosage of wet-torrefied microalgal biochar for MB and CR dyes removal were determined at 1 g/L and 2 g/L, respectively, with their natural pHs as the optimum adsorption pHs. The determined equilibrium contact times for MB and CR were 120 h and 4 h, respectively. Based on the equilibrium modeling, the results revealed that Langmuir isotherm showed the best model fit, based on the highest R² coefficient, for both the adsorption processes of MB and CR using the wet-torrefied microalgal biochar, indicating that the monolayer adsorption was the dominant process. From the modeling, the maximum adsorption capacities for MB and CR were 113.00 mg/g and 164.35 mg/g, respectively. The kinetic modeling indicated the adsorption rate and mechanism of the dyes adsorption processes, which could be crucial for future modeling and application of wet-torrefied microalgal biochar. From the results, it suggests that the valorization of microalgae by utilizing wet-torrefied microalgal biochar as the effective adsorbent for the removal of toxic dyes with an approach of microalgal biorefinery and value-added application to the environment is feasible.

Maintaining thyroid homeostasis during pregnancy is vital for fetal development. The few studies that have investigated associations between metal exposure and gestational thyroid function have yielded mixed findings. To evaluate the association of exposure to a mixture of toxic metals with thyroid parameters in 824 pregnant women from the Rhea birth cohort in Crete, Greece. Concentrations of three toxic metals [cadmium (Cd), antimony (Sb), lead (Pb)] and iodine were measured in urine using inductively coupled plasma mass spectrometry and thyroid hormones [Thyroid Stimulating Hormone (TSH), free thyroxine (fT4), and free triiodothyronine (fT3)] were measured in serum in early pregnancy. Associations of individual metals with thyroid parameters were assessed using adjusted regression models, while associations of the metal mixture with thyroid parameters were assessed using Bayesian Kernel Machine Regression (BKMR).Women with high (3rd tertile) concentrations of urinary Cd, Sb and Pb, respectively, had 13.3 % (95%CI: 2.0 %, 23.2 %), 12.5 % (95%CI: 1.8 %, 22.0 %) and 16.0 % (95%CI: 5.7 %, 25.2 %) lower TSH compared to women with low concentrations (2nd and 1st tertile). In addition, women with high urinary Cd had 2.2 % (95%CI: 0.0 %, 4.4 %) higher fT4 and 4.0 % (95%CI: −0.1 %, 8.1 %) higher fT3 levels, and women with high urinary Pb had 4 % (95%CI: 0.2 %, 8.0 %) higher fT3 levels compared to women with low exposure. The negative association of Cd with TSH persisted only when iodine sufficiency was unfavorable. BKMR attested that simultaneous exposure to toxic metals was associated with decreased TSH and increased fT3 and revealed a potential synergistic interaction of Cd and Pb in association with TSH. The present results suggest that exposure to toxic metals even at low levels can alter gestational thyroid homeostasis.

Selenium (Se) and arsenic (As) are toxic contaminants in surface water and drinking water. The human body needs little quantity of Se, but too high dose is not allowed. Metal oxides such as iron oxides were used for adsorption or co-precipitation removal of As from water. However, the regeneration and stability problems of metals oxides sorbents are unsatisfactory , and there is not enough adsorbent for Se removal from water also. We developed the acrylic amine fiber (AAF) for adsorption reomval of Se and As from water and systematically studied the influenced factors. Batch experiments were conducted for investigating the adsorption edges, while column filtration tests were employed for dynamic application edges. At neutral pH, the Langmuir isotherm fittings gave the maximum adsorption capacities of As(V), As(III), Se(VI) and Se(IV) are 270.3, 40.5, 256.4, and 158.7 mg/g, respectively. Effects of co-existing inorganic anions on As(V) and Se(VI) adsorption using AAF gave the order of PO₄³⁻ > SO₄²⁻ > NO₃⁻ > SiO₃²⁻, while different organic acids obey the order of citric acid > oxalic acid > formic acid. Fourier transform infrared analysis showed the PO₄³⁻ and SO₄²⁻ competition mechanisms are electrostatic repulsions, while the competition of organic acids derived from acid-base reaction between the carboxyl group and the amino group. Column filtration and regeneration results showed that the spent AAF can be regenerated using 0.5 mol/L HCl solution and reused with no much decrease of adsorption capacity.

Samples of ambient PM₂.₅ were collected in the Qingdao harbor area between 21 March and May 25, 2016, and analyzed to investigate the compositions and sources of PM₂.₅ and to assess source-specific selected toxic element health risks to workers via a combination of positive matrix factorization (PMF) and health risk (HR) assessment models. The mean concentration of PM₂.₅ in harbor area was 48 μg m⁻³ with organic matter (OM) dominating its mass. Zn and V concentrations were significantly higher than the other selected toxic elements. The hazard index (HI) and cancer risk (Rᵢ) of all selected toxic elements were lower than the United States Environmental Protection Agency (USEPA) limits. There were no non-cancer and cancer risks for workers in harbor area. The contributions from industrial emissions (IE), ship emissions (SE), vehicle emissions (VE), and crustal dust and coal combustion (CDCC) to selected toxic elements were 39.0%, 12.8%, 24.0%, and 23.0%, respectively. The HI values of selected toxic elements from IE, CDCC, SE, and VE were 1.85 × 10⁻¹, 7.08 × 10⁻², 6.36 × 10⁻², and 3.37 × 10⁻², respectively; these are lower than the USEPA limits. The total cancer risk (Rₜ) value from selected toxic elements in CDCC was 2.04 × 10⁻⁷, followed by IE (6.40 × 10⁻⁸), SE (2.26 × 10⁻⁸), and VE (2.18 × 10⁻⁸). CDCC and IE were the likely sources of cancer risk in harbor area. The Bo Sea and coast were identified as the likely source areas for health risks from IE via potential source contribution function (PSCF) analysis based on the results of PMF-HR modelling. Although the source-specific health risks were below the recommended limit values, this work illustrates how toxic species in PM₂.₅ health risks can be associated with sources such that control measures could be undertaken if the risks warranted it.

During the current pandemic, chemical disinfectants are ubiquitously and routinely used in community environments, especially on common touch surfaces in public settings, as a means of controlling the virus spread. An underappreciated risk in current regulatory guidelines and scholarly discussions, however, is that the persisting input of chemical disinfectants can exacerbate the growth of biocide-tolerant and antibiotic-resistant bacteria on those surfaces and allow their direct transfers to humans. For COVID-19, the most commonly used disinfecting agents are quaternary ammonium compounds, hydrogen peroxide, sodium hypochlorite, and ethanol, which account for two-thirds of the active ingredients in current EPA-approved disinfectant products for the novel coronavirus. Tolerance to each of these compounds, which can be either intrinsic or acquired, has been observed on various bacterial pathogens. Of those, mutations and horizontal gene transfer, upregulation of efflux pumps, membrane alteration, and biofilm formation are the common mechanisms conferring biocide tolerance in bacteria. Further, the linkage between disinfectant use and antibiotic resistance was suggested in laboratory and real-life settings. Evidence showed that substantial bacterial transfers to hands could effectuate from short contacts with surrounding surfaces and further from fingers to lips. While current literature on disinfectant-induced antimicrobial resistance predominantly focuses on municipal wastes and the natural environments, in reality the community and public settings are most severely impacted by intensive and regular chemical disinfecting during COVID-19 and, due to their proximity to humans, biocide-tolerant and antibiotic-resistant bacteria emerged in these environments may pose risks of direct transfers to humans, particularly in densely populated urban communities. Here we highlight these risk factors by reviewing the most pertinent and up-to-date evidence, and provide several feasible strategies to mitigate these risks in the scenario of a prolonging pandemic.