The largest and most variable step of selenium (Se) assimilation into aquatic ecosystems is the rapid uptake of aqueous Se by primary producers. These organisms can transfer more harmful forms of Se to higher trophic levels via dietary pathways, although much uncertainty remains around this step of Se assimilation due to site-specific differences in water chemistry, hydrological and biogeochemical characteristics, and community composition. Thus, predictions of Se accumulation are difficult, and boreal lake systems are relatively understudied. To address these knowledge gaps, five static-renewal field experiments were performed to examine the bioaccumulation of low, environmentally relevant concentrations of Se, as selenite, by naturally grown periphyton from multiple boreal lakes. Periphyton rapidly accumulated Se at low aqueous Se concentrations, with tissue Se concentrations ranging from 8.0 to 24.9 μg/g dry mass (dm) in the 1–2 μg Se/L treatments. Enrichment functions ranged from 2870 to 12 536 L/kg dm in the 4 μg Se/L treatment, to 11 867–22 653 L/kg dm in the 0.5 μg Se/L treatment among lakes. Periphyton Se uptake differed among the five study lakes, with periphyton from mesotrophic lakes generally accumulating more Se than periphyton from oligotrophic lakes. Higher proportions of charophytes and greater dissolved inorganic carbon in more oligotrophic lakes corresponded to less periphyton Se uptake. Conversely, increased proportions of bacillariophytes and total dissolved phosphorus in more mesotrophic lakes corresponded to greater periphyton Se uptake. Periphyton community composition and water chemistry variables were correlated, limiting interpretation of differences in periphyton Se accumulation among lakes. The results of this research provide insight on the biodynamics of Se assimilation at the base of boreal lake food webs at environmentally relevant concentrations, which can potentially inform ecological risk assessments in boreal lake ecosystems in North America.

Recently, a novel method for carbon capture and storage has been proposed, which converts gaseous CO2 into aqueous bicarbonate ions (HCO3−), allowing it to be deposited into the ocean. This alkalinization method could be used to dispose large amounts of CO2 without acidifying seawater pH, but there is no information on the potential adverse effects of consequently elevated HCO3− concentrations on marine organisms. In this study, we evaluated the ecotoxicological effects of elevated concentrations of dissolved inorganic carbon (DIC) (max 193 mM) on 10 marine organisms. We found species-specific ecotoxicological effects of elevated DIC on marine organisms, with EC50-DIC (causing 50% inhibition) of 11–85 mM. The tentative criteria for protecting 80% of individuals of marine organisms are suggested to be pH 7.8 and 11 mM DIC, based on acidification data previously documented and alkalinization data newly obtained from this study. Overall, the results of this study are useful for providing baseline information on ecotoxicological effects of elevated DIC on marine organisms. More complementary studies are needed on the alkalinization method to determine DIC effects on seawater chemistry and marine organisms.

While evidence indicates that groundwater is a potential source for greenhouse gas (GHG) emissions, information for such emissions in groundwater used for irrigation is lacking. Based on 23 wells in the mid-western Guanzhong Basin of China, we investigated the dissolved CO₂, N₂O, and CH₄ distributions in groundwater, their relationships with water indicators, and emission fluxes during flood irrigation. We found zero methane, but CO₂ and N₂O were 30 and 25 times, respectively, supersaturated compared to atmospheric concentrations. Dissolved N₂O in groundwater was positively correlated with NO₃⁻-N (P = 0.009), while CO₂ depended mainly on low pH and high dissolved inorganic carbon. The CO₂ and N₂O emission fluxes detected in wellheads, especially in shallow wells, implied potential emissions. Flood irrigation experiments showed that 24.55% of dissolved CO₂ and 36.81% of dissolved N₂O in groundwater was degassed immediately (within 12 min of irrigation) to the atmosphere. Our study demonstrates that direct GHG emissions from groundwater used for agricultural irrigation in the Guanzhong Basin are potentially equivalent to about 2–4% of the GHG emissions from 3 years of fertilizer use on these farmlands, so further research should focus on optimizing irrigation strategies to mitigate GHG emissions.

The aragonite saturation state (Ωₐᵣₐg) was determined to assess its seasonal variations and the major controlling factors in the southeastern Yellow Sea (YS) over four seasons. Ωₐᵣₐg showed large seasonal variation in the surface waters, with dissolved inorganic carbon (DIC) as a major factor controlling the seasonal variation. In the bottom waters, Ωₐᵣₐg exhibited only small seasonal variation compared with the surface waters; DIC and total alkalinity were the main factors contributing to the variation. The bottom water of the southeastern YS was undersaturated with aragonite during the fall, even though the southeastern YS was not typically associated with upwelling, freshwater discharge, or eutrophication processes. Aragonite undersaturation was most likely due to ocean dumping of organic materials. Therefore, ocean pumping should be prohibited in shallow marginal seas to prevent aragonite undersaturation.

Ecosystem uptake and transfer of Sellafield-derived radiocarbon (14C) were examined within the West of Scotland marine environment. The dissolved inorganic carbon component of seawater, enriched in 14C, is transported to the West of Scotland where it is transferred through the marine food web. Benthic and pelagic biota with variable life-spans living in the North Channel and Clyde Sea show comparable 14C activities. This suggests that mixing of 14C within the Irish Sea results in a relatively constant northwards dispersal of activity. Benthic species in the Firth of Lorn have similar 14C enrichments, demonstrating that Irish Sea residual water is the dominant source to this area. Measured 14C activities in biota show some similarity to western Irish Sea activities, indicating that dispersion to the West of Scotland is significant with respect to the fate of Sellafield 14C releases. Activities measured in commercially important species do not pose any significant radiological risk.

We investigated the growth and nutrient uptake of Myriophyllum spicatum under different nutrient conditions and evaluated its implications for ecosystem services in an enclosed area of Jinshan. The specific growth rate ranged from 1.29%–4.37%/day, and the dissolved inorganic carbon and nitrogen, and phosphorus uptake rates were 1.30–1.62, 0.040–0.453, and 0.003–0.027 mg/(g∙day), respectively, under different nutrient conditions. The O₂-production and carbon-sequestration efficiencies in the field were 154.30 and 1.25 mg/(g DW∙h), respectively. The average removal efficiencies of NH₄⁺-N, NO₃⁻-N, NO₂⁻-N, and PO₄³⁻-P were 43.05%, 97.03%, 64.26%, and 59.24%, respectively, in M. spicatum-cultivated areas compared with in the open sea. Harvesting of M. spicatum removed 12,936.87, 1289.97 and 114.81 kg of carbon, nitrogen, and phosphorus, respectively, from seawater in Jinshan in Nov, 2018. In conclusion, M. spicatum is a good candidate for integrated macrophyte/animal multi-trophic aquaculture in terms of nutrient extraction and economic diversification in low-salinity environments.

The dynamics of the aragonite saturation state (Ωarag) were investigated in the eutrophic coastal waters of Guanabara Bay (RJ-Brazil). Large phytoplankton blooms stimulated by a high nutrient enrichment promoted the production of organic matter with strong uptake of dissolved inorganic carbon (DIC) in surface waters, lowering the concentrations of dissolved carbon dioxide (CO2aq), and increasing the pH, Ωarag and carbonate ion (CO32−), especially during summer. The increase of Ωarag related to biological activity was also evident comparing the negative relationship between the Ωarag and the apparent utilization of oxygen (AOU), with a very close behavior between the slopes of the linear regression and the Redfield ratio. The lowest values of Ωarag were found at low-buffered waters in regions that receive direct discharges from domestic effluents and polluted rivers, with episodic evidences of corrosive waters (Ωarag<1). This study showed that the eutrophication controlled the variations of Ωarag in Guanabara Bay.

Wastewater disposal often has deleterious impacts on the receiving environment. Low dissolved oxygen levels are particularly concerning. Here, we investigate the impacts on dissolved oxygen and carbon chemistry of screened municipal wastewater in the marine waters off Victoria, Canada. We analyzed data from undersea moorings, ship-based monitoring, and remotely-operated vehicle video. We used these observations to construct a two-layer model of the nearfield receiving environment. Despite the lack of advanced treatment, dissolved oxygen levels near the outfalls were well above a 62 μmol kg⁻¹ hypoxic threshold. Furthermore, the impact on water column oxygen at the outfall is likely <2 μmol kg⁻¹. Dissolved inorganic carbon is not elevated and pH not depressed compared to the surrounding region. Strong tidal currents and cold, well-ventilated waters give Victoria's marine environment a high assimilative capacity for organic waste. However, declining oxygen levels offshore put water near the outfall at risk of future hypoxia.

We investigated the aragonite saturation state (Ωarag) during all four seasons in a coastal region of southern Korea that receives considerable freshwater input. The surface Ωarag values were higher during productive seasons with enhanced freshwater influences, likely due to an increased net removal of dissolved inorganic carbon (DIC) from the water column (i.e., biological control). In addition, during the productive seasons, enhancement of Ωarag was observed with decreasing salinity within a linear mixing zone present between river-influenced surface and saltier bottom waters. DIC appeared to be effectively sequestered from the warmer, less salty surface water by downward flux of organic matter, but not significantly affected by the relatively DIC-rich, cooler and saltier bottom waters under strong stratification conditions during these seasons (i.e., physical control). Low phytoplankton productivity and seasonal breakdown of the stratification caused reduced saturation in other seasons and made the study area a weak sink for atmospheric CO2.

In this work, the results of hydrochemical studies aboard the R/V Iran Behshahr in southern Caspian Sea in late-winter 2014 were presented. Salinity, temperature, dissolved oxygen, pH, total dissolved inorganic carbon, total alkalinity, nitrate, phosphate and silicate concentrations in water column of Neka-Amir Kabir oil platform section in the southern Caspian Sea were measured to study the status of hydrochemistry of this area. Results showed that the hypoxia continues to intensify in the deep-water basin of the South Caspian Sea. Near-zero concentration of dissolved oxygen and accumulation of phosphate, silicate and total dissolved inorganic carbon in near-bottom layers in the study area showed that vertical winter mixing of water column did not reach the near-bottom layers at the time of this survey. Nitrate showed its maximum concentration at the intermediate maximum depth of 300m.