The increasing human presence is having an impact on plateau ecosystems, but the special environment and lack of data make it difficult to assess the real ecological risks of pharmaceutical and personal care products (PPCPs) in the river of plateau. The occurrence, distribution and trophic transfer of nineteen PPCPs were investigated in the middle and lower reaches of the Yarlung Zangbo River on the Tibetan Plateau. All the targeted PPCPs were detected in filtrated water, and seventeen PPCPs were detected in the colloid, sediment and suspended particulate matter (SPM). The distribution coefficients of colloid-infiltration water (IFW) were 1–2 orders of magnitude larger than those in the SPM-IFW, which were 1–2 orders of magnitude greater than those in the sediment-IFW. Colloids are sinks for PPCPs with up to 78.55% of the water being in the colloidal phase, in which important factors such as protein and protein-like substances are found. PPCPs in the rivers of the plateau showed high bioaccumulation ability. The fugacity-based bioaccumulation model was established and revealed that the fish in the Tibetan Plateau ingested PPCPs mainly through water instead of food and excreted them mainly through metabolism. In addition, the trophic dilution effect in the food web was observed with trophic magnification factors ranging from 0.06 to 0.22. The positive correlation between the Kd in the colloid-IFW and the bioaccumulation factors implied that natural colloids can not only regulate the behaviour of PPCPs in the environment, but also play an important role in bioaccumulation, which may affect the scientific nature of biological risk assessment.

Microplastic pollution is widely recognised as a global issue, posing risks to natural ecosystems and human health. The combination of rapid industrial and urban development and relatively limited environmental regulation in many tropical countries may increase the amount of microplastic entering rivers, but basic data on contamination levels are lacking. This is especially the case in tropical South East Asian countries. In this paper, the abundance, composition and spatio-temporal variation of microplastic in the Langat River, Malaysia, were assessed, and the relationship between microplastic concentration and river discharge was investigated. Water samples were collected over a 12-month period from 8 sampling sites on the Langat, extending from forested to heavily urbanised and industrial areas. All 508 water samples collected over this period contained microplastic; mean concentration across all sites and times was 4.39 particles/L but extended up to 90.00 particles/L in some urban tributaries. Most microplastics were secondary in origin, and dominated by fibres. Microplastic counts correlated directly with river discharge, and counts increased and decreased in response to changes in flow. A time-integrated assessment of the microplastic load conveyed by the Langat suggested that the river is typically (50 % of the time) delivering around 5 billion particles per day to the ocean. The positive correlation between the concentration of microplastics and suspended sediments in the Langat suggested that continuously logging turbidity sensors could be used to provide better estimates of microplastic loads and improve assessment of human and ecological health risks.

Sete Cidades Lake (São Miguel Island, Portugal) is subdivided into two interconnected branches: the Green Lake and Blue Lake. The lake has an area and maximum depth of 4.39 km² and 29.5 m (Blue Lake), respectively, with evidence of eutrophication, particularly in the northern area of the Green Lake. In this study, we conducted a sampling survey during January 2017 to measure CO₂ fluxes from the lake using a floating accumulation chamber. We also produced two hydrogeochemical profiles for each of the lake’s branches. A total of 1760 CO₂ flux measurements were taken along the lake’s surface. The lake water was relatively cold (14.0 °C on average) and weakly mineralised (average electrical conductivity of 116 μS cm⁻¹) with a neutral pH (7.7 on average). The relative composition of major ions occurred in the following decreasing order: Na⁺ > Mg²⁺ > Ca²⁺ > K⁺ for cations and Cl⁻ > HCO₃⁻ > SO₄²⁻ for anions. The lake water was mainly the Na–Cl type due to sea salt input from seawater spraying. CO₂ fluxes ranged from 0.3 to 17.2 g m⁻² d⁻¹ and from 2.1 to 17.9 g m⁻² d⁻¹ for the Blue and Green Lakes, respectively. Highest CO₂ degassing occurred in areas dominated by macrophytes and algal blooms. The measured values suggest that the CO₂ was predominantly biogenically sourced, which was further supported by the δ¹³C isotopic data. The estimated total CO₂ emissions varied between 5.8 t d⁻¹ (Green Lake; area = 0.81 km²) and 24.9 t d⁻¹ (Blue Lake; area = 3.58 km²). This study further elucidates the lake’s trophic and chemical pollution status and has major implications for lacustrine CO₂ emissions to the atmosphere. Our study also provides a reference for understanding potential future variations in volcanic activity.

The determination of both stable nitrogen (δ¹⁵N–NO₃⁻) and stable oxygen (δ¹⁸O–NO₃⁻) isotopic signatures of nitrate in PM₂.₅ has shown potential for an approach of assessing the sources and oxidation pathways of atmospheric NOx (NO+NO₂). In the present study, daily PM₂.₅ samples were collected in the megacity of Beijing, China during the winter of 2017–2018, and this new approach was used to reveal the origin and oxidation pathways of atmospheric NOx. Specifically, the potential of field δ¹⁵N–NO₃⁻ signatures for determining the NOx oxidation chemistry was explored. Positive correlations between δ¹⁸O–NO₃⁻ and δ¹⁵N–NO₃⁻ were observed (with R² between 0.51 and 0.66, p < 0.01), and the underlying environmental significance was discussed. The results showed that the pathway-specific contributions to NO₃⁻ formation were approximately 45.3% from the OH pathway, 46.5% from N₂O₅ hydrolysis, and 8.2% from the NO₃+HC channel based on the δ¹⁸O-δ¹⁵N space of NO₃⁻. The overall nitrogen isotopic fractionation factor (εN) from NOx to NO₃⁻ on a daily scale, under winter conditions, was approximately +16.1‰±1.8‰ (consistent with previous reports). Two independent approaches were used to simulate the daily and monthly ambient NOx mixtures (δ¹⁵N-NOx), respectively. Results indicated that the monthly mean values of δ¹⁵N-NOx compared well based on the two approaches, with values of −5.5‰ ± 2.6‰, −2.7‰ ± 1.9‰, and −3.2‰ ± 2.2‰ for November, December, and January (2017–2018), respectively. The uncertainty was in the order of 5%, 5‰ and 5.2‰ for the pathway-specific contributions, the εN, and δ¹⁵N-NOx, respectively. Results also indicated that vehicular exhaust was the key contributor to the wintertime atmospheric NOx in Beijing (2017–2018). Our advanced isotopic perspective will support the future assessment of the origin and oxidation of urban atmospheric NOx.

Phosphorus-inactivating agents (PIAs) as geoengineering tools in lakes have been investigated extensively, but PIA resuspension in the photic layer occurs frequently in shallow lakes and little is known about the influence of algae on PIA performance. Our results proved that algae increased the dissolved oxygen, pH and dissolved organic carbon concentration substantially. In the absence of sediment, lanthanum modified zeolite (LMZ) as a representative PIA and algae could deplete dissolved inorganic phosphorus (DIP) from water but the former was faster than the latter. When LMZ and algae coexisted, the amount of phosphorus that was captured by LMZ was 3.1 times greater than that taken up by algae. An increase in pH or dissolved organic carbon increased the zero-equilibrium phosphorus concentration (EPC₀) of the sediment but LMZ addition could lower the EPC₀ and reduce the risk of phosphorus release during the algal blooming season. In the presence of sediment, LMZ reduced the DIP concentration more rapidly and yielded a lower final DIP concentration compared with algae. In conclusion, the influence of algae on the performance of LMZ by (i) taking up DIP to reduce the availability of DIP and convert DIP into a releasable phosphorus form and (ii) increasing the pH and dissolved organic carbon concentration to hinder the adsorption ability of DIP were recognized. The LMZ performed well, even in the presence of algae.

Dissolved organic matter (DOM) and dissolved ions are two integral parameters to affect the environmental fate of As in different ways. Numerous studies chose surrogate of DOM, humic substances (HSs), to investigate the As complexation behavior. However, microbial secretion (protein and polysaccharide) was also considered for a great proportion in surface aquatic system, and its effect was still not fully understood. The present research distinguished the As complexation behavior with different DOM components (HSs, protein, polysaccharide and synthetic organic matter) in natural and simulated water samples. The results indicated that different DOM components exhibited various binding capacities for As. HSs showed the strongest affinity for As, followed by long-chain compounds (polysaccharide and synthetic organic matter) and proteins. In water source, HSs were probably the primary parameter for As complexation. In eutrophic water system, however, polysaccharide maybe the main DOM component to bind As. Cationic bridge function was prone to occur in the presence of HSs, but not observed in the presence of protein. PO₄³⁻ competed for binding sites with As, consequently decreasing the As complexation with all the DOM components. The research implied that a comprehensive and meticulous analyses of DOM fractions and coexist ions are the prerequisite to understanding the behavior of As (or other pollutants) in different natural aquatic systems.

Plastic pollution in the world's ocean is one of the major environmental challenges that affects the society today, due to their persistence at sea, adverse consequences to marine life and being potentially harmful to human health. Rivers are now widely recognized as being the major input source of land-based plastic waste into the seas. Despite their key role in plastic transportation, riverine plastic pollution research is still in its infancy and plastic sources, hot-spots and degradation processes in riverine systems are to date poorly understood. In this contribution, we introduce a novel concept of following the aging of polypropylene based post-consumer goods placed in known trapping and mobility zones of macroplastics on a fluvial point bar, which was determined through repeated field surveys of macroplastic densities on this bar. As a proof-of-concept, we followed the degradation of 5 identical plastic butter tubs in 5 different locations on a riverbank and significant differences in the aging of the tubs were observed. The degree of aging of the tubs can to some extent be correlated to their proximity to the main river channel, exposure to natural conditions, such as solar radiation, and its storage time on land.

Cadmium (Cd) and lead (Pb) are ubiquitously present in surface soils, due to anthropogenic activities, causing threat to ecological and human health because of their carcinogenic nature. They accumulate in large quantities in the environment and affect negatively soil microbiota, plants, animals, and humans. For the cleanup of Cd/Pb polluted soils, different plant species have been studied. Many plants have shown the potential to hyperaccumulate Cd/Pb in their above-ground tissues. These plants decrease soil pH by root exudation or by releasing H⁺ ions, and this, in turn, increases the bioavailability of Cd/Pb for plant uptake. Different environmental processes related to soil organic matter, microorganisms, pH, genetic modifications, and various soil-borne chelating agents affect the potential of phytoremediation technology. Review papers trying to identify a single factor influencing the phytoremediation of heavy metals are available in the literature. However, an integrated approach dealing with different factors involved in the remediation of both metals is scarcely discussed. The main focus of this review is to discuss the phytoextraction technique for Cd/Pb removal from contaminated sites along with detoxification mechanisms. Further, the challenges in the Cd/Pb phytoextraction and different options available to cope with these challenges are also discussed. The update on the relevant findings on the use of microorganisms and amendments in enhancing the Cd/Pb phytoextraction is also provided. Finally, the areas to be explored in future research for the removal of Cd/Pb by integrated strategies have been discussed.

Rumen liquid can effectively degrade lignocellulosic biomass, in which rumen microorganisms play an important role. In this study, transformation of bacterial community structure in rumen liquid anaerobic digestion of rice straw was explored. Results showed that rice straw was efficiently hydrolyzed and acidified, and the degradation efficiency of cellulose, hemicellulose and lignin reached 46.2%, 60.4%, and 12.9%, respectively. The concentration of soluble chemical oxygen demand (SCOD) and total volatile fatty acid (VFA) reached 12.9 and 8.04 g L⁻¹. The high-throughput sequencing results showed that structure of rumen bacterial community significantly changed in anaerobic digestion. The Shannon diversity index showed that rumen bacterial diversity decreased by 32.8% on the 5th day of anaerobic digestion. The relative abundance of Prevotella and Fibrobacter significantly increased, while Ruminococcus significantly decreased at the genus level. The Spearman correlation heatmap showed that pH and VFA were the critical factors affecting the rumen bacterial community structure. The function prediction found that rumen bacteria mainly functioned in carbohydrate transport and metabolism, which might contain a large number of lignocellulose degrading enzyme genes. These studies are conducive to the better application of rumen microorganisms in the degradation of lignocellulosic biomass.

To characterize the emissions of polycyclic aromatic hydrocarbons (PAHs) from residential biomass burning and coal combustion in field environments, smoke samples were collected from the combustion of six types of biomass in heated kangs and four types of coal in traditional stoves and semi-gasifier stoves. The emission factors (EFs) of the total PAH were in the range of 84.5–344 mg/kg for biomass burning, with lower EFs for biomass with higher densities, and in the range of 38.0–206 mg/kg for coal combustion, with lower EFs for coals with higher maturity. Moreover, EFs were lower from high-density biomass fuels (wood trunk, 84.5 ± 11.3 mg/kg) than low-maturity coals (bituminous coal, 206 ± 16.5 mg/kg). Parent, oxygenated, alkylated, and nitrated PAHs accounted for 81.1%, 12.6%, 6.2%, and 0.1%, respectively, of the total-PAH EFs from biomass burning, and 84.7%, 13.8%, 1.4%, and 0.1%, respectively, of the total-PAH EFs from coal combustion. PAH source profiles differed negligibly between biomass fuels but differed significantly between bituminous coal and anthracite coal fuels. The characteristic species of sources were phenanthrene, 9-fluorenone, and 2-nitrobiphenyl for biomass burning, and were phenanthrene, benzo[ghi]perylene, 1,4-naphthoquinone, and 2-nitrobiphenyl for coal combustion. The ratios of benzo[b]fluoranthene/(benzo[b]fluoranthene + benzo[k]fluoranthene) were 0.40–0.45 for biomass burning and 0.89–0.91 for coal combustion, and these significantly different values constitute unique markers for distinguishing these fuels in source apportionment. Benzo[a]pyrene-equivalent factor emissions were 2.79–11.3 mg/kg for biomass and 7.49–41.9 mg/kg for coal, where parent PAHs contributed 92.0%–95.1% from biomass burning and 98.6%–98.8% from coal combustion. Total-PAH emissions from residential heating were 1552 t across Shaanxi province, to which wheat straw (445 t) in biomass burning and bituminous coal (438 t) in coal combustion were the highest contributors. Results from this study provide crucial knowledge for the source identification of PAHs as well as for the design of abatement strategies against pollutant emissions.