Dissolved organic matter (DOM) and carbon nanotubes are introduced into aquatic environments. Thus, it is important to elucidate whether their interaction affects DOM amount and composition. In this study, the composition of DOM, before and after interactions with single-walled carbon nanotubes (SWCNTs), was measured and the adsorption affinity of the individual structural fractions of DOM to SWCNTs was investigated. Adsorption of DOM to SWCNTs was dominated by the hydrophobic acid fraction, resulting in relative enhancement of the hydrophilic character of non-adsorbed DOM. The preferential adsorption of the HoA fraction was concentration-dependent, increasing with increasing concentration. Adsorption affinities of bulk DOM calculated as the normalized sum of affinities of the individual structural fractions were similar to the measured affinities, suggesting that the structural fractions of DOM act as independent adsorbates. The altered DOM composition may affect the nature and reactivity of DOM in aquatic environments polluted with carbon nanotubes.

Understanding future climate change requires accurate estimates of the impacts of atmospheric nitrogen (N) deposition, composed of both inorganic and organic compounds, on greenhouse gas (GHG) fluxes in grassland ecosystems. However, previous studies have focused on inorganic compounds and have not considered the potential effects of organic N sources. Here, we conducted a grassland experiment that included organic, inorganic N, and a mix of them at a ratio of 4:6, with two input rates, to study N inputs induced CO₂, CH₄, and N₂O fluxes, as well as the potential abiotic and biotic mechanisms driving the fluxes. We found that N compositions significantly affected fluxes each of the three GHGs. Greater organic N decreased the impacts of N addition on CO₂ and N₂O emissions, caused primarily by low rates of increase in substrates (soil available N) for production of CO₂ and N₂O resulting from high ammonia volatilization rather than changes in microbial activity. Also, greater organic N slightly stimulated CH₄ uptake. Nitrogen composition effects on CO₂ emissions and CH₄ uptake were independent of N input rates and measurement dates, but N₂O emissions showed stronger responses to inorganic N under high N addition and in June. These results suggest that future studies should consider the source of N to improve our prediction of future climate impact of N deposition, and that management of N fertilization can help mitigate GHG emissions.

A comprehensive study was carried out from central part of Indo-Gangetic Plain (IGP; at Kanpur) to understand abundance, temporal variability, processes (secondary formation and fog-processing) and source-apportionment of PM₁-bound species (PM₁: particulate matter of aerodynamic diameter ≤ 1.0 μm) during wintertime. A total of 50 PM₁ samples were collected of which 33 samples represent submicron aerosol characteristics under non-foggy condition whereas 17 samples represent characteristics under thick foggy condition. PM₁ mass concentration during non-foggy episodes varied from 24–393 (Avg.: 247) μg m⁻³, whereas during foggy condition it ranged from 42–243 (Avg.: 107) μg m⁻³. With respect to non-foggy condition, the foggy conditions were associated with higher contribution of PM₁-bound organic matter (OM, by 23%). However, lower fractional contribution of SO₄²⁻, NO₃⁻ and NH₄⁺ during foggy conditions is attributable to wet-scavenging owing to their high affinity to water. Significant influence of fog-processing on organic aerosols composition is also reflected by co-enhancement in OC/EC and WSOC/OC ratio during foggy condition. A reduction by 5% in mineral dust fraction under foggy condition is associated with a parallel decrease in PM₁ mass concentration. However, mass fraction of elemental carbon (EC) looks quite similar (≈3% of PM₁) but the mass absorption efficiency (MAE) of EC is higher by 30% during foggy episodes. Thus, it is evident from this study that fog-processing leads to quite significant enhancement in OM (23%) contribution (and MAE of EC) with nearly equal and parallel decrease in SO₄²⁻, NO₃⁻ and NH₄⁺ and mineral dust fractions (totaling to 24%). Characteristic features of mineral dust remain similar under foggy and non-foggy conditions; inferred from similar ratios of Fe/Al (≈0.3), Ca/Al (0.35) and Mg/Al (0.22). Positive matrix factorization (PMF) resolves seven sources: biomass burning (19.4%), coal combustion (1.1%), vehicular emission (3%), industrial activities (6.1%), leather tanneries (4%), secondary transformations (46.2%) and mineral dust (20.2%).

In this paper, results from receptor modelling performed on a well-characterised PM₁ dataset were combined to chemical light extinction data (bₑₓₜ) with the aim of assessing the impact of different PM₁ components and sources on light extinction and visibility at a European polluted urban area. It is noteworthy that, at the state of the art, there are still very few papers estimating the impact of different emission sources on light extinction as we present here, although being among the major environmental challenges at many polluted areas. Following the concept of the well-known IMPROVE algorithm, here a tailored site-specific approach (recently developed by our group) was applied to assess chemical light extinction due to PM₁ components and major sources.PM₁ samples collected separately during daytime and nighttime at the urban area of Milan (Italy) were chemically characterised for elements, major ions, elemental and organic carbon, and levoglucosan. Chemical light extinction was estimated and results showed that at the investigated urban site it is heavily impacted by ammonium nitrate and organic matter. Receptor modelling (i.e. Positive Matrix Factorization, EPA-PMF 5.0) was effective to obtain source apportionment; the most reliable solution was found with 7 factors which were tentatively assigned to nitrates, sulphates, wood burning, traffic, industry, fine dust, and a Pb-rich source. The apportionment of aerosol light extinction (bₑₓₜ,ₐₑᵣ) according to resolved sources showed that considering all samples together nitrate contributed at most (on average 41.6%), followed by sulphate, traffic, and wood burning accounting for 18.3%, 17.8% and 12.4%, respectively.

Urban black-odor water (BOW) is a typical phenomenon seen in the urban water environment; it is caused by excessive pollution by organic matter and other pollutants, such as nitrogen and phosphorous. Chromophoric dissolved organic matter (CDOM) is a major optical fraction of dissolved organic matter. In this study, optical properties and components of CDOM were obtained from 178 river samples collected from five cities in China, the sample were investigated using absorption and fluorescence spectroscopy. The collected included 89 ordinary water (OW) samples, 63 mild BOW (MBOW), and 26 heavy BOW (HBOW) samples. Significant differences were found in the absorption spectra of the HBOW, MBOW, and OW samples, particularly in their optical parameters (the slope of the spectrum (S₂₇₅₋₂₉₅), and the ratio of two absorption coefficients of CDOM (E₂:E₃)). Additionally, the fluorescence intensity of the humic acid-like component (F₅) and soluble microbial by product-like component (F₄) obtained via the fluorescence regional integration (FRI) method were 3 and 4.2 times higher in HBOW than in OW, respectively; this could be used as an indicator to distinguish OW from BOW in urban rivers. The results obtained using the redundancy method and the strong negative correlation between F₄ and dissolved oxygen (DO) (r = − 0.56) suggested that the composition of CDOM could change significantly under different urban water environments (p < 0.01). Different correlations were also found between F₅, and a355, E₂:E₃, S₂₇₅₋₂₉₅ in different BOW levels, suggesting that the optical parameters of CDOM were mainly determined by the polluted organic matter originating from terrestrial sources with large molecular humic acid-like compounds; optical parameter a355 could distinguish BOW from OW. These findings are conducive in understanding the dynamics of organic matter pollution and to discover the composition and optical properties of the CDOM in urban BOW and OW, thereby providing an effective method for tracking the spatial characteristics of BOW in urban rivers using remote sensing technologies in areas with multiple sources of pollution.

This study reports comprehensive analysis of seasonal and inter-annual variations of aerosol properties (optical, physical and chemical) and radiative effects over Pokhara Valley in the foothills of central Himalayas in Nepal utilizing the high-quality multi-year columnar aerosol data observed recently from January 2010 to December 2017. This paper focusses on the seasonal and inter-annual variations of chemical (composition), and absorption properties of aerosols and their radiative effects. The single scattering albedo (SSA) either decreases as a function of wavelength or remains independent of wavelength. The seasonal mean aerosol absorption optical depth (AAOD) exhibits a behavior opposite to that of SSA. Carbonaceous aerosols (CA) dominate (≥60%) aerosol absorption during the whole year. Black carbon (BC) alone contributes >60% to AAODCA while brown carbon (BrC) shares the rest. The absorbing aerosol types are determined to be BC, and mixed (BC and dust) only. Dust as absorbing aerosol type is absent over the Himalayan foothills. The ARFSFC is ≥ -50 Wm⁻² except in monsoon almost every year. The ARFATM is ≥ 50 Wm⁻² during winter and pre-monsoon in all the years. ARFESFC, ARFETOA and ARFEATM follow a similar pattern as that of ARF. High values of ARFE at SFC, TOA and ATM (except during monsoon when values are slightly lower) suggest that aerosols are efficient in significantly modulating the incoming solar flux throughout the year. The annual average aerosol-induced atmospheric heating rate (HR) over Pokhara is nearly 1 K day⁻¹ every year during 8-year observation, and is highest in 2015 (∼2.5 K day⁻¹). The HR is about 1 K day⁻¹ or more over all the locations in IGP during the year. These quantitative results can be used as inputs in global/regional climate models to assess the climate impact of aerosols, including on regional temperature, hydrological cycle and melting of glaciers and snowfields in the region.

Syringic acid, which is a typical methoxyphenol emitted from wood combustion, can provide heterogeneous reaction sites for gaseous active components, influencing the concentrations of trace gases and the compositions of syringic acid. The heterogeneous uptake of O₃ on syringic acid was investigated using a flow tube reactor under ambient pressure. The initial uptake coefficient (γᵢ) and the steady-state uptake coefficient (γₛₛ) of O₃ linearly increased with syringic acid mass (0–0.16 μg cm⁻²) and temperature (278–328 K), while they decreased with increasing the O₃ concentration and the O₂ content. The γᵢ was independent of relative humidity (20%–70%), whereas γₛₛ decreased with relative humidity (7%–70%). The compositional changes of syringic acid by the ozonization were analyzed by the Fourier transform infrared spectrometer (FT-IR) and the gas chromatography-mass spectrometry (GC-MS), confirming the generation of 2,6-dimethoxy-1,4-benzoquinone. In addition, compared to that of fresh syringic acid, the mass absorption efficiency of syringic acid aged by O₃ exhibited an increase in the range of 290–320 nm.

To identify the sources and heterogeneous reactions of sulfate and nitrate with dust in the atmosphere, airborne particles in Xi'an, inland China during the spring of 2017 were collected and measured for chemical compositions, along with a laboratory simulation of the heterogeneous formation of ammonium nitrate on the dust surface. Our results showed that concentrations of Ca²⁺, Na⁺ and Cl⁻ in the TSP samples were enhanced in the dust events, with the values of 41.8, 5.4 and 4.0 μg m⁻³, respectively, while NO₃⁻ (7.1 μg m⁻³) and NH₄⁺ (2.4 μg m⁻³) remarkably decreased, compared to those in the non-dust periods. During the dust events, NH₄⁺ correlated only with NO₃⁻ (R² = 0.52) and abundantly occurred in the coarse mode (>2.1 μm), in contrast to that in the non-dust periods, which well correlated with sulfate and nitrate and enriched in the fine mode (<2.1 μm). SO₄²⁻ in Xi'an during the dust events existed mostly as gypsum (CaSO₄·2H₂O) and mirabilite (Na₂SO₄·10H₂O) and dominated in the coarse mode, suggesting that they were directly transported from the upwind Gobi Desert region. Our laboratory simulation results showed that during the long-range transport hygroscopic salts in the Gobi dust such as mirabilite can absorb water vapor and form a liquid phase on the particle surface, then gaseous NH₃ and HNO₃ partition into the aqueous phase and form NH₄NO₃, resulting in the strong correlation of NH₄⁺ with NO₃⁻ and their accumulation on dust particles. The dry deposition flux of total inorganic nitrogen (NH₄⁺ + NO₃⁻) in Xi'an during the dust events was 0.97 mg-N m⁻² d⁻¹ and 37% higher than that in the non-dust periods. Such a significant enhanced N-deposition is ascribed to the heterogeneous formation of NH₄NO₃ on the dust particle surface, which has been ignored and should be included in future model simulations.

Seafloor litter was investigated in the Bohai Sea, Yellow Sea, and northern East China Sea (BYnECS) based on fisheries-independent bottom trawl surveys in 2019. The mean density of seafloor litter was 48.44 items∙km⁻² (44.56 kg∙km⁻²) in the BYnECS, which was at an intermediate level compared with the values observed in other continental shelf areas worldwide. There were significant differences in the density of seafloor litter among different regions (P < 0.05), and the high-density litter accumulation areas in the northern Yellow Sea and Changjiang estuary and adjacent waters were close to the sediment accumulation areas. Plastics were predominant in the BYnECS and accounted for 72.80%/44.05% (number/weight) of the seafloor litter. Fishery-related litter was the main source of seafloor litter in the BYnECS. This study systematically reports the density, composition, sources and spatial distribution of seafloor litter in the BYnECS, thereby providing a scientific basis for the management of marine litter.