Evaluation of MERRA-2 and CAMS reanalysis for black carbon aerosol in China.

Black carbon (BC) constitutes a pivotal component of atmospheric aerosols, significantly impacting regional and global radiation balance, climate, and human health. In this study, we evaluated BC data in two prominent atmospheric composition reanalysis datasets: the Modern-Era Retrospective analysis for Research and Applications, Version 2 (MERRA-2) and the Copernicus Atmosphere Monitoring Service (CAMS), and analyzed the causes of their deviations. This assessment is based on observational data collected from 34 monitoring stations across China from 2006 to 2022. Our research reveals a significant and consistent decline in BC concentrations within China, amounting to a reduction exceeding 67.33%. However, both MERRA-2 and CAMS reanalysis data fail to capture this declining trend. The average annual decrease of BC in MERRA-2 from 2006 to 2022 is only 0.06 µg/m3 per year, while the BC concentration in CAMS even increased with an average annual value of 0.014 µg/m3 per year. In 2022, MERRA-2 had overestimated BC concentration by 20% compared to observational data, while CAMS had overestimated it by approximately 66%. In the regional BC concentration analysis, the data quality of the reanalysis data is better in the South China (RM = 0.59, RC = 0.53), followed by the North China (RM = 0.50, RC = 0.42). Reanalysis BC data in Northwest China and the Tibetan Plateau are difficult to use for practical analysis due to their big difference with observation. In a comparison of the anthropogenic BC emissions inventory used in the two atmospheric composition reanalysis datasets with the Multi-resolution Emission Inventory model for Climate and air pollution research (MEIC) emissions inventory, we found that: Despite the significant decline in China's BC emissions, MERRA-2 still relies on the 2006 emissions inventory, while CAMS utilizes emission inventories that even show an increasing trend. These factors will undoubtedly lead to greater deviations between reanalysis and observational data.

An analysis of atmospheric stability indices and parameters under air pollution conditions.

The stability of the atmosphere plays an important role in changes in air pollutant concentrations. Stable atmospheric conditions cause pollutant concentrations to reach high values, which degrades the air quality in a particular region. This study aims to reveal the relationship between atmospheric stability indices/parameters (thermodynamic indices) and changes in air pollutant concentrations. Pollutant concentrations of PM10, PM2.5, SO2, NO2, CO, and O3 were statistically analyzed for a 10-year (2013-2022) period for nine air quality stations located in the megacity Istanbul. Based on national and international air quality standards, 145 episode days were determined for the days when these parameters exceeded the threshold values. Five stability indices (Showalter Index - SI, Lifted Index - LI, Severe Weather Index - SWEAT, K Index - KI, Totals Totals Index - TTI), and three stability parameters (Convective Available Potential Energy - CAPE, Convective Inhibition - CIN, Bulk Richardson Number - BRN) were used to determine the stability of the atmosphere for episode days. It has been found that in cases where air pollutant concentrations are high, the stability parameters reveal the stability of the atmosphere better than the stability indices. It was also found that there was at least one vertical inversion layer on 122 of the 145 episode days, these layers mostly (84%) occurred between the surface and 850 hPa levels, and the layer thicknesses were mostly between 0-250 m (84%).

Sources, size-resolved deposition in the human respiratory tract and health risks of submicron black carbon in urban atmosphere in Pearl River Delta, China.

Black carbon (BC) has a significantly negative impact on air quality, climate and human health. Here we investigated the sources and health effects of BC in urban area of the Pearl River Delta (PRD) based on online data measured by Aerodyne soot particle high-resolution time of flight aerosol mass spectrometer (SP-AMS). In urban PRD, BC particles mainly came from vehicle emissions especially heavy-duty vehicle exhausts (contributing 42.9 % of total BC mass concentration), long-range transport (27.6 %), and aged biomass combustion emissions (22.3 %). Indicated by source analysis using simultaneous aethalometer data, BC associated with local secondary oxidation and transport may also be originated from fossil fuel combustion, especially traffic sources in urban and surrounding areas. Size-resolved BC mass concentrations provided by SP-AMS, for the first time to our best knowledge, were used to calculate BC deposition in the human respiratory tract (HRT) of different populations (children, adults, and the elderly) by the Multiple-Path Particle Dosimetry (MPPD) model. We found that submicron BC was deposited more in the pulmonary (P) region (49.0-53.2 % of the total BC deposition dose), while less in the tracheobronchial (TB, 35.6-37.2 %) and head (HA, 11.2-13.8 %) regions. Adults suffered the highest BC deposition (1.19 µg day-1) than the elderly (1.09 µg day-1) and children (0.25 µg day-1). BC deposition rate was greater at night (especially 18:00-24:00) than during the daytime. The maximum deposition in the HRT was found for BC particles around 100 nm, mainly in deeper respiratory regions (TB and P), which may cause more serious health effects. Adults and the elderly group are confronted with the notable carcinogenic risk of BC in the urban PRD, up to 29 times higher than the threshold. Our study emphasizes the need to control BC pollution in the urban area, especially nighttime vehicle emissions.

Effect of modified atmosphere packaging with different gas mixtures on the texture and muscle proteins of Pacific white shrimp (Litopenaeus vannamei) during cold storage.

In this study, the effect of modified atmosphere packaging with different gas mixtures on texture and muscle properties of Pacific white shrimp (Litopenaeus vannamei) during refrigerated storage was studied via texture profile, water holding capacity (WHC), protein properties (Ca2+-ATPase, TCA-soluble peptides, myofibrillar/sarcoplasmic protein content), and microbial counts. The results showed that the antibacterial effect of Modified atmosphere packaging (MAP) was correlated with the increase of CO2 with the presence of low level of O2. Though MAP without O2 had a higher whiteness value but also had higher bacterial counts and total volatile basic nitrogen (TVB-N) values compared with other MAP-groups. In general, a gas composition of 80% CO2 + 5%O2 + 15% N2 treatment had lowest microbial counts and reduced TVB-N values by 22.85% in comparison with the control on day 10. However, MAP was found to have a complicated impact on muscle protein and texture of shrimp. 60% CO2 + 5% O2 + 35% N2 and 40% CO2 + 5% O2 + 55% N2 had an advantage in maintaining springiness and the content of myofibrillar/sarcoplasmic proteins. The correlation analysis showed that WHC had stronger relationship with springiness, resilience, myofibrillar protein content. Therefore, regarding the texture and protein properties, the concentration of CO2 in MAP for Pacific white shrimp should not be higher than 60%.

Evaluation of the CAMS reanalysis for atmospheric black carbon and carbon monoxide over the north China plain.

Black carbon (BC) and carbon monoxide (CO) at different model levels from the Copernicus Atmosphere Monitoring Service (CAMS) reanalysis were comprehensively evaluated against observations performed simultaneously on both surface and mountain sites in winter and summer in the North China Plain for the first time. CAMS could capture the seasonal difference in BC and CO emission on both sites but showed significant and persistent biases. Biases were high on the surface site and low on the mountain site for both seasons, implying the uncertainties in emission inventories used in the CAMS reanalysis which may have more influence near source. Biases were reduced and the correlation coefficient of CAMS BC with observed BC increased when two datasets were compared on a daily basis, which suggests daily or longer time averaged CAMS BC could be more suitable for trend analysis. Although CAMS could generally reproduce the distinct diurnal variation of BC and CO on both sites, the inaccurate representation of the daily evolution of planetary boundary layer (PBL) in model may bring more uncertainties to the concentration biases on surface from midnight to early morning. BC hydrophilic ratio from CAMS displayed large biases compared to observations with no seasonal difference on both sites, which was probably resulted from the initial emission state of BC hygroscopicity for all source types in model. Uncertainties in the removal processes and the simplified aging processes in model could further induce uncertainty in modelling BC hydrophilic ratio in the CAMS. These results could not only be referenced for the improvement on CAMS reanalysis but also facilitate model or trend analysis of BC and CO pollution by utilizing the CAMS reanalysis product from both short- and long-term perspectives, which will be beneficial to both the mitigation and policy-making on primary emissions in China.

Precipitation scavenging of beryllium-7 (7Be): Observation results and parameterization.

This study aims to develop a 1D model that makes it possible to calculate the daily total 7Be wet deposition flux. For this purpose, long-term (2015-2021), high-frequency (daily) and time-synchronized series of observations of 7Be wet deposition flux and its atmospheric activity concentration are analyzed in this paper. Daily mean 7Be activity concentration in the atmosphere, daily total 7Be wet deposition flux and mean 7Be activity concentration, washout ratio, deposition velocity and scavenging coefficient with individual precipitation events lie in the range of 0.1-17 mBq m-3, 0.8-117.2 Bq m-2 d-1, 0.4-11.3 Bq L-1, 331-3799, 0.2-24.7 cm s-1 and (0.8-35.6) × 10-5 s-1, respectively. Quantitative estimates of the influence of precipitation parameters (amount, intensity and duration) on the daily total 7Be wet deposition flux, mean 7Be activity concentration in precipitation, washout ratio, deposition velocity and scavenging coefficient with individual precipitation events have been obtained using correlation analysis. It has been found that precipitation amount has the greatest influence on 7Be deposition flux and deposition velocity, precipitation intensity has the greatest influence on washout ratio and scavenging coefficient, and precipitation duration has the greatest influence on 7Be activity concentration in precipitation. The relationships between these parameters have been parameterized. Based on these parameterizations, five 1D models that calculate the daily total 7Be wet deposition flux have been introduced and validated against the observation data. It has been revealed that the model, which is based on deposition velocity parameterization and uses the data on 7Be activity concentration in the atmosphere and the daily amount of precipitation as predictors, reproduces the highest fraction of the observational data (88%) with the lowest average calculation error (32%) compared to the other four models.

The response of soil-atmosphere greenhouse gas exchange to changing plant litter inputs in terrestrial forest ecosystems.

Various global change factors (e.g. elevated CO2 concentrations, nitrogen deposition, etc.) can alter the amount of litterfall in terrestrial forests, which could subsequently lead to changes in the physical, chemical, and biological properties of forest soils. Yet, there is hitherto a lack of consensus on the role of litter in governing the soil-atmosphere exchange of greenhouse gases (GHGs) in forest ecosystems, which can significantly affect the overall climatic cooling impacts of forests as a net carbon sink. In this study, we carried out a meta-analysis of over 250 field observations to determine the response of soil GHG fluxes to in situ litter manipulation in global forests. Our results showed that overall, litter addition enhanced soil CO2 emissions from terrestrial forests by 26%, while litter removal reduced soil CO2 emissions from these forests by 26%. The negative response of soil CO2 emissions to litter removal was stronger in the tropical forests (-33%) than in the subtropical (-27%) and temperate (-21%) forests, and was significantly correlated with mean annual temperature and precipitation. Moreover, litter removal was observed to enhance soil CH4 uptake in tropical (+24%) and temperate (+9%) forests, but not in subtropical forests. Litter removal reduced N2O emissions from forest soils by 20% on average, with this negative effect increasing with mean annual precipitation. The duration of litter removal experiment was negatively correlated with the response of soil CO2 emissions but had no influence on the response of soil CH4 and N2O fluxes. We found that plant litter supply could alter soil GHG fluxes in forests by modulating the microclimate as well as the labile and recalcitrant soil carbon pools. Our findings highlighted the importance of considering the effects of changing plant litter inputs on soil-atmosphere GHG fluxes in terrestrial forests and their spatio-temporal variability in biogeochemical models.

A miniature chemiluminescence spectrometric system induced by atmosphere microplasma jet to avoid using hydrogen peroxide and catalyst.

A miniature luminol chemiluminescence system based on atmosphere microplasma is proposed for detection without any catalysts. In our research, atmosphere microplasma jet is employed to oxidize luminol and produce chemiluminescence instead of H2O2. The transport of OH radicals to the plasma-liquid interface and induce the chemiluminescence. The weight of the system is only 3.6 kg (including a 1.2 kg laptop), and the power consumption of the microplasma is only 0.045 W. The mechanism of luminol chemiluminiscence induced by microplasma jet and generation of microplasma jet are investigated in this study. A 1 mL sample solution is sufficient for trace 3-NPA determination within an analysis time of 6 min. In the range of 0.03-10 mg L-1, 3-NPA can be quantitatively analyzed along with a detection limit of 0.008 mg L-1. In addition, the proposed system is employed for real-world samples detection, including water samples, brown sugar and tainted sugarcane, which demonstrates the reliability and practical feasibility of the detection method.

Pesticides in the atmosphere and seawater in a transect study from the Western Pacific to the Southern Ocean: The importance of continental discharges and air-seawater exchange.

The global oceans are known as terminal sink or secondary source for diffusive emission of organochlorine pesticides (OCPs) and selected current used pesticides (CUPs) into the overlaying atmosphere. Many pesticides have been widely produced worldwide, subsequently applied, and released into the environment. However, information on the occurrence patterns, spatial variability, and air-seawater exchange of pesticides is limited to easily accessible regions and, hence, only few studies are reported from the remote Southern Ocean. To fill this information gap, a large-scale ship-based sampling campaign was conducted. In the samples from this campaign, we measured concentrations of 221 pesticides. Both gaseous and aqueous samples were collected along a sampling transect from the western Pacific to the Southern Ocean (19.75° N-76.16° S) from November 2018 to March 2019. Twenty-seven individual pesticides were frequently (≥ 50%) detected in gaseous and aqueous samples. Tebuconazole, diphenylamine, myclobutanil, and hexachlorobenzene (HCB) dominated the composition profile in both phases. Spatial trends analysis in atmospheric and seawater concentrations showed a substantial level reduction from the western Pacific towards the Southern Ocean. Back-trajectory analysis showed that atmospheric pesticide concentrations were strongly influenced by air masses origins. Continental and riverine inputs are important sources of pesticides in the western Pacific and Indian Oceans. Atmospheric and seawater concentrations for the target pesticide residues in the Southern Ocean are low and evenly distributed due to the large distance from potential pollution sources as well as the effective isolation by the Antarctic Convergence (AC). Air-seawater fugacity ratios and fluxes indicated that the western Pacific and Indian Oceans were secondary sources for most pesticides emitted to the atmosphere, while the Southern Ocean was still considered to be a sink.

Wetting properties of fresh urban soot particles: Evaluation based on critical supersaturation and observation of surface trace materials.

Soot particles strongly absorb solar radiation and contribute to global warming. Also, wetting properties of soot at emission can affect its lifetime. We investigated surface conditions related to wetting and hydrophobic properties of fresh soot using data from measurements taken in Tokyo. A cloud condensation nuclei (CCN) counter was used to clarify surface conditions of particles composed mainly of water-insoluble (WI) materials: total and active particles as CCN around critical supersaturation (Sc) of 203-nm-diameter WI particles. Averaged number fractions of inactivated particles as CCN at 1.05% supersaturation (SS), which is Sc of hydrophilic WI particles, were estimated as 1.4%. Number fractions of inactive particles changed less at 1.78%SS during rush hour and increased at 0.89%SS, implying that most of the WI particles included small amounts of water-soluble (WS) materials rather than being completely hydrophobic. Based on transmission electron microscope (TEM) analysis of samples collected during rush hour, 69% of the mostly bare soot particles had Na or K small domains that are regarded as originating in fossil fuels. Based on water dialysis analysis results, some Na and K on soot were WS. Combination results with CCN measurements suggest that these WS materials decrease the Sc of soot. Moreover, the morphological structure of sulfate covering Na and K domains on the soot surface implicates pre-existing sodium and potassium compounds on soot as a trigger of soot aging. However, inactive particles at Sc at poor-hydrophilic particles and soot particles composed solely of WI materials on TEM samples were also found, although they were minor. Such particles, which are unfavorable for obtaining a wettable surface, might retain non-hygroscopicity for a longer period in the atmosphere. Evaluation of long-range soot transport can benefit from consideration of slight and inhomogeneous differences of chemical compounds on soot that occur along with their emission.

Statistical analysis, source apportionment, and toxicity of particulate- and gaseous-phase PAHs in the urban atmosphere.

Introduction: The concentrations of particulate and gaseous Polycyclic Hydrocarbons Carbon (PAHs) were determined in the urban atmosphere of Delhi in different seasons (winter, summer, and monsoon). Methodology: The samples were collected using instrument air metric (particulate phase) and charcoal tube (gaseous phase) and analyzed through Gas chromatography. The principal component and correlation were used to identify the sources of particulate and gaseous PAHs during different seasons. Results and discussion: The mean concentration of the sum of total PAHs (TPAHs) for particulate and gaseous phases at all the sites were found to be higher in the winter season (165.14 ± 50.44 ng/m3 and 65.73 ± 16.84 ng/m3) than in the summer season (134.08 ± 35.0 ng/m3 and 43.43 ± 9.59 ng/m3), whereas in the monsoon season the concentration was least (68.15 ± 18.25 ng/m3 and 37.63 1 13.62 ng/m3). The principal component analysis (PCA) results revealed that seasonal variations of PAHs accounted for over 86.9%, 84.5%, and 94.5% for the summer, monsoon, and winter seasons, respectively. The strong and positive correlation coefficients were observed between B(ghi)P and DahA (0.922), B(a)P and IcdP (0.857), and B(a)P and DahA (0.821), which indicated the common source emissions of PAHs. In addition to this, the correlation between Nap and Flu, Flu and Flt, B(a)P, and IcdP showed moderate to high correlation ranging from 0.68 to 0.75 for the particulate phase PAHs. The carcinogenic health risk values for gaseous and particulate phase PAHs at all sites were calculated to be 4.53 × 10-6, 2.36 × 10-5 for children, and 1.22 × 10-5, 6.35 × 10-5 for adults, respectively. The carcinogenic health risk for current results was found to be relatively higher than the prescribed standard of the Central Pollution Control Board, India (1.0 × 10-6).

Dominance of the residential sector in Chinese black carbon emissions as identified from downwind atmospheric observations during the COVID-19 pandemic.

Emissions of black carbon (BC) particles from anthropogenic and natural sources contribute to climate change and human health impacts. Therefore, they need to be accurately quantified to develop an effective mitigation strategy. Although the spread of the emission flux estimates for China have recently narrowed under the constraints of atmospheric observations, consensus has not been reached regarding the dominant emission sector. Here, we quantified the contribution of the residential sector, as 64% (44-82%) in 2019, using the response of the observed atmospheric concentration in the outflowing air during Feb-Mar 2020, with the prevalence of the COVID-19 pandemic and restricted human activities over China. In detail, the BC emission fluxes, estimated after removing effects from meteorological variability, dropped only slightly (- 18%) during Feb-Mar 2020 from the levels in the previous year for selected air masses of Chinese origin, suggesting the contributions from the transport and industry sectors (36%) were smaller than the rest from the residential sector (64%). Carbon monoxide (CO) behaved differently, with larger emission reductions (- 35%) in the period Feb-Mar 2020, suggesting dominance of non-residential (i.e., transport and industry) sectors, which contributed 70% (48-100%) emission during 2019. The estimated BC/CO emission ratio for these sectors will help to further constrain bottom-up emission inventories. We comprehensively provide a clear scientific evidence supporting mitigation policies targeting reduction in residential BC emissions from China by demonstrating the economic feasibility using marginal abatement cost curves.

The Seasonality Impact of the BTEX Pollution on the Atmosphere of Arad City, Romania.

Benzene, toluene, and total BTEX (benzene, toluene, ethylbenzene, and xylene) concentrations registered for one year (2016) have been determined every month for one high-density traffic area. The assessment was performed in Arad City, Romania, to evaluate these pollutants and their influence on the inhabitants' health. The contaminants were sampled using a static sampling method and analyzed by gas chromatography coupled with mass spectrometry. Benzene was the most dominant among the BTEX compounds-the average concentrations ranged from 18.00 ± 1.32 µg m-3 in December to 2.47 ± 0.74 µg m-3 in August. The average toluene concentration over the year was 4.36 ± 2.42 µg m-3 (with a maximum of 9.60 ± 2.39 µg m-3 in November and a minimum of 1.04 ± 0.29 µg m-3 in May). The toluene/benzene ratio (T/B) was around 0.5, indicating substantial contributions from mobile sources (vehicles). The emission and accumulation of different aromatic compounds (especially benzene) could deteriorate the urban air quality. The lifetime cancer risk (LTCR) for benzene was found to be more than 10-5 in winter, including the inhabitants in the "probable cancer risk" category.

Investigation of Venus Cloud Aerosol and Gas Composition Including Potential Biogenic Materials via an Aerosol-Sampling Instrument Package.

A lightweight, low-power instrument package to measure, in situ, both (1) the local gaseous environment and (2) the composition and microphysical properties of attendant venusian aerosols is presented. This Aerosol-Sampling Instrument Package (ASIP) would be used to explore cloud chemical and possibly biotic processes on future aerial missions such as multiweek balloon missions and on short-duration (<1 h) probes on Venus and potentially on other cloudy worlds such as Titan, the Ice Giants, and Saturn. A quadrupole ion-trap mass spectrometer (QITMS; Madzunkov and Nikolic, J Am Soc Mass Spectrom 25:1841-1852, 2014) fed alternately by (1) an aerosol separator that injects only aerosols into a vaporizer and mass spectrometer and (2) the pure aerosol-filtered atmosphere, achieves the compositional measurements. Aerosols vaporized <600°C are measured over atomic mass ranges from 2 to 300 AMU at <0.02 AMU resolution, sufficient to measure trace materials, their isotopic ratios, and potential biogenic materials embedded within H2SO4 aerosols, to better than 20% in <300 s for H2SO4 -relative abundances of 2 × 10-9. An integrated lightweight, compact nephelometer/particle-counter determines the number density and particle sizes of the sampled aerosols.

Characteristics, toxicity, source identification and seasonal variation of atmospheric polycyclic aromatic hydrocarbons over East India.

Atmospheric PM2.5-bound polycyclic aromatic hydrocarbons (PAHs) were analyzed over urban and rural sites during January to December 2018. Total annual average concentration of PM2.5 was 74.41 ± 24.96 µg/m3 over urban and 52.03 ± 13.11 µg/m3 over rural site during study time. The annual average concentration of PM2.5 over urban and rural atmospheres were found approximately twice in urban and found also higher over rural site, with respect to National Ambient Air Quality (NAAQ) standard of 40 µg/m3 for PM2.5 concentration. The annual concentration of PAHs was 750.80 ± 19.49 ng/m3 over urban, and, over rural, it was 559.59 ± 17.56 ng/m3. The seasonal variation of concentration of PAHs was in order of winter > post-monsoon > summer > monsoon. The most predominant PAHs were IcP (17.21%), B(ghi) P(15.22%), BkF (11.60%), DBahA (11.34%) and BbF (10.91%) to the total PAH concentration over urban site; over rural site, most predominant PAHs were IcP (16.02%), B(ghi)P, (15.63%), BkF (11.46%), DBahA (11.12%) and BbF (8.99%) of total PAHs. DBahA concentration was contributed approximately 46% carcinogenicity over both urban and rural sites, and BaP contributes 33.56% carcinogenicity over urban site and 34.62% carcinogenicity over rural site of total PAH samples. The Excess Life Time Cancer Risk (ELCR) values over urban were found at acceptable limit 10-6-10-4 given by the United States Environmental Protection Agency. Over rural site, the ELCR value was found near about acceptable limit. Diagnostic ratio analysis demonstrated that major sources of PAHs were pyrogenic sources and vehicular emission over study. Air parcel through trajectories over study site also contributed in PAH concentration.

Investigation of distribution, transportation, and impact factors of atmospheric black carbon in the Arctic region based on a regional climate-chemistry model.

Black carbon (BC) as the main component of pollutants in the Arctic plays an important role on regional climate change. In this study, we applied the regional climate-chemistry model, WRF-Chem, to investigate the spatial distribution, transportation, and impact factors of BC in the Arctic. Compared with reanalysis data and observations, the WRF-Chem performed well in terms of the seasonal variations of meteorological parameters and BC concentrations, indicating the applicability of this model on Arctic BC simulation works. Our results showed that the BC concentrations in the Arctic had an obviously seasonalvariation pattern. Surface BC concentrations peaked during winter and spring seasons, while the minimum occurred during summer and autumn seasons. For the vertical distribution, BC aerosols mainly concentrated in the Arctic lower troposphere, and most of BC distributed near the surface during winter and spring seasons and in the higher altitude during other seasons. The seasonality of BC was associated with the seasonal change of meteorological field. During winter, the significant northward airflow prevailing in northern Eurasia caused the transport of accumulated pollutants from this region into the Arctic. The similar but weakened northward airflow pattern and the anticyclone activity during spring can allow pollutants to be transported to the Arctic lower troposphere. Moreover, the more stable atmosphere during winter and spring seasons made BC accumulated mainly near the surface. During summer and autumn seasons, the less stable boundary layer and the cyclone activity in the Arctic facilitated the diffusion of pollutants into the higher altitude. Meanwhile, the higher relative humidity can promote the wet removal process and lead to the relatively lower BC concentrations near the surface. Compared with the seasonal change of emission, our analysis showed that the seasonal variation of meteorological field was the main contributor for the seasonality of BC in the Arctic.

Phosphine as a Biosignature Gas in Exoplanet Atmospheres.

A long-term goal of exoplanet studies is the identification and detection of biosignature gases. Beyond the most discussed biosignature gas O2, only a handful of gases have been considered in detail. In this study, we evaluate phosphine (PH3). On Earth, PH3 is associated with anaerobic ecosystems, and as such, it is a potential biosignature gas in anoxic exoplanets. We simulate the atmospheres of habitable terrestrial planets with CO2- and H2-dominated atmospheres and find that PH3 can accumulate to detectable concentrations on planets with surface production fluxes of 1010 to 1014 cm-2 s-1 (corresponding to surface concentrations of 10s of ppb to 100s of ppm), depending on atmospheric composition and ultraviolet (UV) irradiation. While high, the surface flux values are comparable to the global terrestrial production rate of methane or CH4 (1011 cm-2 s-1) and below the maximum local terrestrial PH3 production rate (1014 cm-2 s-1). As with other gases, PH3 can more readily accumulate on low-UV planets, for example, planets orbiting quiet M dwarfs or with a photochemically generated UV shield. PH3 has three strong spectral features such that in any atmosphere scenario one of the three will be unique compared with other dominant spectroscopic molecules. Phosphine's weakness as a biosignature gas is its high reactivity, requiring high outgassing rates for detectability. We calculate that tens of hours of JWST (James Webb Space Telescope) time are required for a potential detection of PH3. Yet, because PH3 is spectrally active in the same wavelength regions as other atmospherically important molecules (such as H2O and CH4), searches for PH3 can be carried out at no additional observational cost to searches for other molecular species relevant to characterizing exoplanet habitability. Phosphine is a promising biosignature gas, as it has no known abiotic false positives on terrestrial planets from any source that could generate the high fluxes required for detection.

A perspective on the development of gas-phase chemical mechanisms for Eulerian air quality models.

An essential component of a three-dimensional air quality model is its gas-phase mechanism. We present an overview of the necessary atmospheric chemistry and a discussion of the types of mechanisms with some specific examples such as the Master Chemical Mechanism, the Carbon Bond, SAPRC and the Regional Atmospheric Chemistry Mechanism (RACM). The first versions of the Carbon Bond and SAPRC mechanisms were developed through a hierarchy of chemical species approach that relied heavily on chemical environmental chamber data. Now a new approach has been proposed where the first step is to develop a highly detailed explicit mechanism such as the Master Chemical Mechanism and the second step is to test the detailed explicit mechanism against laboratory and field data. Finally, the detailed mechanism is condensed for use in a three-dimensional air quality model. Here it is argued that the development of highly detailed explicit mechanisms is very valuable for research, but we suggest that combining the hierarchy of chemical species and the detailed explicit mechanism approaches would be better than either alone.Implication: Many gas-phase mechanisms are available for urban, regional and global air quality modeling. A "hierarchy of chemical species approach," relying heavily on smog-chamber data was used for the development of the early series of mechanisms. Now the development of large, explicit master mechanisms that may be condensed is a significant, trend. However, a continuing problem with air quality mechanism development is due to the high complexity of atmospheric chemistry and the current availability of laboratory measurements. This problem requires a balance between completeness and speculation so that models maintain their utility for policymakers.

Polycyclic aromatic hydrocarbons in tree barks, gaseous and particulate phase samples collected near an industrial complex in São Paulo (Brazil).

Urban trees are a new tool for pollutant monitoring since gaseous and particulate pollutants can deposit in its barks. Polycyclic aromatic hydrocarbons (PAHs) levels were determined in gaseous phase samples collected in polyurethane foam (PUF), total suspended particles (TSP) samples collected in quartz fiber filters and tree bark samples (Tipuana and Sibipiruna) collected in the surroundings of an industrial complex in the metropolitan area of São Paulo. Benzo(b)fluoranthene presented the highest average concentration in the TSP samples and phenanthrene, the highest average concentration in the PUF samples; the sum of carcinogenic equivalents for benzo(a)pyrene (BaPEq) for both phases was above 20 ng m-3, representing a high cancer risk. The most abundant PAH for tree barks was fluoranthene; low weight PAHs presented a higher abundance than the observed in TSP. Coronene (vehicular exhaust marker) presented good correlations with fluoranthene in the tree bark samples, suggesting an influence of vehicular emissions. A tree bark sample collected near the petrochemical area presented biomarkers of petrogenic origin (hopanoids) in the mass spectrum and an unresolved complex mixture (UCM) profile. The results suggested an influence of both vehicular and industrial sources on the air quality observed in the atmosphere and tree barks samples.

Application of thermal desorption methods for airborne polycyclic aromatic hydrocarbon measurement: A critical review.

Thermal desorption (TD) is a universal solvent-free pre-concentration technique. It is often used to pre-concentrate semi-volatile and volatile organic compounds in various sample types. Polycyclic aromatic hydrocarbons (PAHs) are widespread contaminants from incomplete combustion of organic matter and fossil fuel, which have carcinogenic effects on human health. Conventional methods for determining PAHs, represented by solvent extraction, are gradually being replaced by solvent-free methods, typically the TD technique, because of TD's many advantages, including time savings and environmentally friendly treatment. This work presents an extensive review of the universal methods used to determine PAHs in the atmosphere based on the TD technique. The methods currently used for collection and detection of both gas- and particle-phase PAHs in the air are critically reviewed. In addition, the operating parameters of the TD unit are summarized and discussed. The design shortcomings of existing studies and the problems that researchers should address are presented, and promising alternatives are suggested. This paper also discusses important parameters, such as reproducibility and limit of detection, that form a crucial part of quality assurance. Finally, the limitations and the future prospects of the TD technique for use in airborne PAH analyses are addressed. This is the first review of the latest developments of the TD technique for analysis of PAHs and their derivatives in the atmosphere.