Poyang Lake is the largest freshwater lake in China and a globally important wetland with various functions. Exploring the multidecadal trend of water quality and hydroclimatic conditions is important for understanding the adaption of the lake system under the pressure from multiple anthropogenic and meteorological stressors. The present study applied the Mann–Kendall trend analysis and Pettitt test to detect the trend and breakpoints of hydroclimatic, and water quality parameters (from the 1980s to 2018) and the trend of monthly–seasonal ammonia (NH₄-N) and total phosphorus (TP)concentrations (from 2002 to 2018) in Poyang Lake. Results showed that Poyang Lake had undergone a highly significant warming trend from 1980 to 2018, with a warming rate of 0.44 °C/decade in terms of annual daily mean air temperature. The wind speed and water level of the lake presented a highly significant decreasing trend, whereas no notable trend was detected for precipitation variations. The annual mean total nitrogen (TN), NH₄-N, TP, and permanganate index (CODMₙ) concentrations showed significant upward trends from the 1980s to 2018. Remarkable abrupt shifts were detected for TN, NH₄-N, and CODMₙ in around 2003. They were in accordance with the water level breakpoint of the lake, thus implying the important role of hydrological conditions in water quality variations in floodplain lakes. A significant increasing trend has been detected for Chl-a variations during wet season from 2008 to 2018, which could be attributed to the increasing trend of nutrient concentration during the nutrient-limited phase of Poyang Lake. These hydroclimatic and water quality trends suggest a high risk of increasing phytoplankton growth in Poyang Lake. This study thus emphasizes the need for adaptive lake eutrophication management for floodplain lakes, particularly the consideration of the strong trade-off and synergies between hydroclimatic conditions and water quality variations.

In aquatic environments, organisms such as freshwater mussels are likely exposed to complex contaminant mixtures related to industrial, agricultural, and urban activities. With growing interest in understanding the risk that chemical mixtures pose to mussels, this investigation focused on the effects of various waterborne contaminants (ammonia, chloride, copper, and potassium) and selected binary mixtures of these chemicals following a fixed-ratio design to Villosa iris glochidia and juvenile Lampsilis fasciola. In individual exposures, 48-h EC50 values were determined for V. iris glochidia exposed to ammonia chloride (7.4 [95% confidence interval (CI) 6.6–8.2] mg N/L), ammonia sulfate (8.4 [7.6–9.1] mg N/L), copper sulfate (14.2 [12.9–15.4] μg Cu2+/L), potassium chloride (12.8 [11.9–13.7] mg K+/L), potassium sulfate (10.1 [8.9–11.2] mg K+/L), and sodium chloride (480.5 [435.5–525.5] mg Cl−/L). The 7-d LC50 values for juvenile L. fasciola were determined for potassium sulfate (45.0 [18.8–71.2] mg K+/L), and sodium chloride (1738.2 [1418.6–2057.8] mg Cl−/L). In Ontario these waterborne contaminants have been reported to co-occur, with concentrations exceeding the EC10 for both life stages at some locations. Data from binary mixture exposures for V. iris glochidia (chloride-ammonia, chloride-copper, and copper-ammonia) and juvenile L. fasciola (chloride-potassium) were analyzed using a regression-based, dose-response mixture analysis modeling framework. Results from the mixture analysis were used to determine if an additive model for mixture toxicity [concentration addition (CA) or independent action (IA)] best described the toxicity of each mixture and if deviation towards dose-ratio (DR) or dose-level (DL) synergism/antagonism (S/A) occurred. For all glochidia binary mixture exposures, CA was the best fit model with DL deviation reported for the chloride-copper mixture and DR deviation reported for the copper-ammonia mixture. Using the model deviation ratio (MDR), the observed toxicity in all three glochidia mixture exposures were adequately described by both CA (mean = 0.71) and IA (mean = 0.97) whereas the juvenile mixture exposure was only adequately described by CA (mean = 0.64; IA mean = 0.05).

The ammonium sulphate ((NH₄)₂SO₄) in-situ leaching process is the most widely used extraction technology for weathered crust elution-deposited rare earth ores (WCED-REOs). Highly concentrated (NH₄)₂SO₄, a representative leaching agent, is often used in the leaching process of WCED-REOs. However, this in-situ leaching process causes nitrogen pollution in the soil, surrounding surface and ground water due to the high concentrations of (NH₄)₂SO₄ solutions used as a long term leaching agent. To date, the mechanism behind the variations in ammonia nitrogen (AN) in deep soil profiles is unclear. We conducted vertical and lateral soil sampling and analyzed the collected samples for soil moisture, pH, ammonia forms, and AN contents in soil profiles deeper than 500 cm in an in-situ leaching mining area of Ganzhou, Jiangxi Province, southern China. The results show that primary chemical pollutants in the soil are derived from residual leaching agents with high acidities and concentrations of AN. Twelve years after the mining process was completed, the mean pH values of the tailings in the mining area were 3.90 and 4.87 in its lower reaches. Due to the presence of chemical residues, the AN concentration was 12–40 times higher than that of the raw ore soil before it was mined. The percentages of different ammonium forms in the rare earth tailing soil were 65%, 30%, and 5% for the water-soluble, exchangeable, and fixed ammonium forms, respectively. The results of this study support effective prevention and remediation treatment of environmental problems caused by AN pollution of the soil in WCED-REOs.

Emissions of major reactive nitrogen compounds, including nitric oxide (NO), nitrogen dioxide (NO₂) and ammonia (NH₃), from heavy-duty diesel vehicles (HDDVs) place substantial pressure on air quality for many large cities in China. To control nitrogen oxide (NOX) emissions from HDDVs, selective catalytic reduction (SCR) systems have been widely used since the China IV standards. To investigate the impacts of aftertreatment technologies and driving conditions on real-world emissions of reactive nitrogen compounds, a portable emissions measurement system was employed to test eighteen heavy-duty diesel trucks in China. The results showed that the China IV and China V HDDVs with appropriate SCR functionality could reduce NOX emissions by 36% and 53%, respectively, compared to the China III results, although their real-world emissions were still higher than the corresponding emission limits for regulatory engine tests. For these HDDVs, five samples were tested with NH₃ emissions, ranging from 1.67 ppm to 51.49 ppm. The NH₃ emission rates tended to significantly increase under high-speed driving conditions. The results indicate that the current SCR technology may have certain risks in exceeding the future China VI NH₃ limit. However, five China IV/V HDDVs were found to have SCR temperature sensors that were intentionally tampered with, resulting in comparable or even higher NOX emissions and zero NH₃ emissions. Increased NO₂ emissions due to the adoption of diesel oxidation catalysts and diesel particulate filters were also found from our experiments. This study highlights the importance of enhancing in-use compliance requirements and eliminating aftertreatment tampering for China IV and China V HDDVs.

As the most important gas-phase alkaline species, atmospheric ammonia (NH3) contributes considerably to the formation and development of fine-mode particles (PM2.5), which affect air quality and environmental health. Recent satellite-based observations suggest that the North China Plain is the largest agricultural NH3 emission source in China. However, our isotopic approach shows that the surface NH3 in the intraregional urban environment of Beijing-Tianjin-Shijiazhuang is contributed primarily by combustion-related processes (i.e., coal combustion, NH3 slip, and vehicle exhaust). Specifically, the Batch fractionation model was used to describe the partitioning of gaseous NH3 into particles and to trace the near-ground atmospheric NH3 sources. With the development of haze pollution, the dynamics of δ15N-NH4+ were generally consistent with the fractionation model. The simulated initial δ15N-NH3 values ranged from −22.6‰ to −2.1‰, suggesting the dominance of combustion-related sources for urban NH3. These emission sources contributed significantly (92% on hazy days and 67% on clean days) to the total ambient NH3 in urban cities, as indicated by a Bayesian mixing model. Based on the Batch fractionation model, we concluded the following: 1) δ15N-NH4+ can be used to model the evolution of fine-mode aerosols and 2) combustion-related sources dominate the near-ground atmospheric NH3 in urban cities. These findings highlight the need for regulatory controls on gaseous NH3 emissions transported from local and surrounding industrial sources.

A biofouling resistant passive sampler for ammonia, where the semi-permeable barrier is a microporous hydrophobic gas-diffusion membrane, has been developed for the first time and successfully applied to determine the time-weighted average concentration of ammonia in estuarine and coastal waters for 7 days. Strategies to control biofouling of the membrane were investigated by covering it with either a copper mesh or a silver nanoparticle functionalised cotton mesh, with the former approach showing better performance. The effects of temperature, pH and salinity on the accumulation of ammonia in the newly developed passive sampler were studied and the first two parameters were found to influence it significantly. A universal calibration model for the passive sampler was developed using the Group Method Data Handling algorithm based on seawater samples spiked with known concentrations of total ammonia under conditions ranging from 10 to 30 °C, pH 7.8 to 8.2 and salinity 20 to 35. The newly developed passive sampler is affordable, user-friendly, reusable, sensitive, and can be used to detect concentrations lower than the recently proposed guideline value of 160 μg total NH₃–N L⁻¹, for a 99% species protection level, with the lowest concentration measured at 17 nM molecular NH₃ (i.e., 8 μg total NH₃–N L⁻¹ at pH 8.0 and 20 °C). It was deployed at four field sites in the coastal waters of Nerm (Port Phillip Bay), Victoria, Australia. Good agreement was found between molecular ammonia concentrations obtained with passive and discrete grab sampling methods (relative difference, - 12% to - 19%).

The increase of gaseous ammonia (NH₃) concentration in the atmosphere significantly impacts the regional air quality, human health, and the nitrogen cycle of ecosystems. This study aims to verify the reanalyzed product of IASI NH₃ (the ANNI-NH₃-v2.1R-I, hereafter referred to as IASI_NH₃_R) and to analyze the spatial and temporal characteristics of atmospheric NH₃ during 2008–2016 and its underlying influencing factors. Our results show a good agreement between spatial pattern and temporal (annual and monthly) trend of the satellite-derived surface NH₃ concentrations and the measured near-ground NH₃ measurements over different land covers in Eastern China, suggesting the IASI_NH₃_R product can be used to investigate spatial and temporal trends of atmospheric NH₃ concentration. The annual mean NH₃ column concentrations peaked in the North China Plain (averaged 12 × 10¹⁵ mol cm⁻² yr⁻¹) and showed a significant increasing trend at a rate of 0.6 × 10¹⁵ mol cm⁻² yr⁻¹ during the entire period, which can be ascribed to densely populated, intensive agricultural activities and substantial reduction of SO₂ and NO₂ emissions since 2011. The NH₃ column concentrations show a slight increase in winter in most regions of China, probably due to less precipitation amount and increased uncertainty for lower NH₃ columns and the thermal contrast (TC). A large seasonal variation of NH₃ column concentrations was observed, with the highest values in summer and the lowest in autumn. Such seasonal variation is mainly affected by seasonal differences in NH₃ emissions and meteorological conditions. Our results suggest that the current control measures effectively decreased SO₂ and NO₂ pollution but are not yet apparent in the mitigation of atmospheric NH₃ pollution, which also merits more attention considering that no effective measures are being implemented for NH₃ emission control at a regional or national scale in China.

Ammonia (NH₃) emissions could have significant impacts on both ecosystems and human health. Ice cores from the Tibetan Plateau contain information about past ammonium (NH₄⁺) deposition, which could yield important insights into historical NH₃ emissions in the surrounding source regions as well as long-distance NH₄⁺ aerosol transport via atmospheric circulation. In this paper, we present a high-resolution atmospheric NH₄⁺ deposition record for the period, 1951–2008, reconstructed from the Zangser Kangri (ZK) ice core in the northern Tibetan Plateau. An empirical orthogonal function (EOF) analysis of major soluble ions (NH₄⁺, NO₃⁻, SO₄²⁻, Cl⁻, Na⁺, K⁺, Mg²⁺ and Ca²⁺) reveals that EOF 1 has significant loadings of all ions, therefore representing common transport pathways, while EOF 2 is only significantly loaded by NH₄⁺ (0.86) and NO₃⁻ (0.35), suggesting a unique signal possibly representing emissions from the surrounding terrestrial ecosystems on the Tibetan Plateau. Backward trajectory analysis indicates that the air masses over the ZK ice core drilling site primarily come from the northwestern Indian Peninsula. NH₃ emissions from agricultural activities in this area likely contribute to the NH₄⁺ deposition of the ZK ice core via the Indian monsoon. Correlations between EOF 2 time series and temperature, normalized difference vegetation index (NDVI) suggest that increasing temperature and vegetation after 1980 likely promoted NH₃ emissions from terrestrial ecosystems. Our results provide a reliable and valuable assessment of NH₄⁺ deposition from human activities and terrestrial ecosystems in the ZK ice core, and help in understanding air pollution over the past few decades in the northern Tibetan Plateau.

Recycled materials were used in three types of green sorption media for nutrient removal and possible recovery in high nutrient-laden agricultural discharge and stormwater runoff. The three types of green sorption media included in this comparative study were two new aluminum-based green environmental media (AGEM) and one existing iron-filings based green environmental media (IFGEM). The corresponding adsorption isotherm, thermodynamics, and kinetics models were simulated based on isotherm studies to determine their removal efficiency and potential for recovery of nitrate, phosphate, and ammonia when used as a soil amendment in crop fields or in a filter for water treatment. AGEM-2 exhibited the shortest contact time required to achieve nutrient removal above 80% with an average of 7 h, followed by AGEM-1 and IFGEM with 10.6 and 28 h, respectively. Natural soil was included as a control and exhibited minimal nutrient removal. Ammonia, which may be recovered as fertilizer for drop fields in a soil-water-waste nexus, was generated by all three green sorption media mixes, therefore indicating their potential for use as soil amendments in agricultural and forested land after engineering filter applications. The kinetics analysis indicated that nitrate adsorption follows pseudo-first-order kinetics, while phosphate adsorption follows pseudo-second-order kinetics. The Gibbs free energy indicated that most of the adsorption reactions proceeded as exothermic. Lastly, a few equilibrium models, including the Langmuir, Freundlich, First Modified Langmuir, Temkin, Jovanovic, and Elovich models, were ranked and three were selected for use with IFGEM, AGEM-1, and AGEM-2, respectively, as below: (1) Langmuir, (2) Freundlich, and (3) First Modified Langmuir, according to three indices.

MSW landfill releases a lot of harmful pollutants such as H₂S, NH₃, and VOCs. In this study, two laboratory-scale biocovers such as biochar (BC) derived from agricultural & forestry wastes (AFW) pyrolysis, and sludge modified the biochar (SBC) were designed and used to remove the harmful pollutants. In order to understand in-situ biodegradation mechanism of the harmful pollutants by the SBC, the removal performances of the harmful pollutants together with the bacterial community in the BC and SBC were investigated in simulated landfill systems for 60 days comparing with the contrast experiment of a landfill cover soil (LCS). Meanwhile, the adsorption capacities of representative harmful pollutants (hydrogen sulfide, toluene, acetone and chlorobenzene) in the LCS, BC, and SBC were also tested in a fixed bed reactor. The removal efficiencies of the harmful pollutants by the SBC ranged from 95.43% to 100.00%, which was much higher than that of the LCS. The adsorption capacities of the harmful pollutants in the SBC were 4 times higher than that of the LCS since the SBC exhibited higher BET surface and N-containing functional groups. Meanwhile, the biodegradation rates of the harmful pollutants in the SBC were also much higher than that of the LCS since the populations of the bacterial community in the SBC were more abundant due to its facilitating the growth and activity of microorganisms in the porous structure of the SBC. In addition, a synergistic combination of adsorption and biodegradation in the SBC that enhanced the reproduction rate of microorganisms by consuming the absorbed-pollutants as carbon sources, which also contributed to enhance the biodegradation rates of the harmful pollutants.