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The Arctic is warming at more than twice the rate of the global average. This warming is influenced by clouds, which modulate the solar and terrestrial radiative fluxes and, thus, determine the surface energy budget. However, the interactions among clouds, aerosols, and radiative fluxes in the Arctic are still poorly understood. To address these uncertainties, the Ny-Ålesund Aerosol Cloud Experiment (NASCENT) study was conducted from September 2019 to August 2020 in Ny-Ålesund, Svalbard. The campaign’s primary goal was to elucidate the life cycle of aerosols in the Arctic and to determine how they modulate cloud properties throughout the year. In situ and remote sensing observations were taken on the ground at sea level, at a mountaintop station, and with a tethered balloon system. An overview of the meteorological and the main aerosol seasonality encountered during the NASCENT year is introduced, followed by a presentation of first scientific highlights. In particular, we present new findings on aerosol physicochemical and molecular properties. Further, the role of cloud droplet activation and ice crystal nucleation in the formation and persistence of mixed-phase clouds, and the occurrence of secondary ice processes, are discussed and compared to the representation of cloud processes within the regional Weather Research and Forecasting Model. The paper concludes with research questions that are to be addressed in upcoming NASCENT publications.

Reports from Europe and North America suggest that female chronic obstructive pulmonary disease (COPD) patients have a higher symptom burden and mortality than male patients. However, little is known about the management reality of female patients with COPD in Japan. We compared the clinical characteristics of female COPD patients with those of male using the cohort of the COPD Assessment in Practice study, which is a cross-sectional multicenter observational study. Of the 1168 patients, 133 (11.4%) were female. A history of never smoking was higher in females than males (p<0.01). Although there was no difference in age or forced expiratory volume in one second (FEV ) % predicted between the groups, modified medical research council dyspnea scale (mMRC) and number of frequent exacerbators were higher in females (mMRC≥2: p<0.01; number of exacerbations≥2: p=0.011). The mean forced vital capacity and FEV values in females were lower than those in males (p<0.0001 and p<0.0001, respectively). Females were more likely to use long-term oxygen therapy and inhaled corticosteroids than males (p=0.016 and p<0.01, respectively). The prevalence of the Global Initiative for Chronic Obstructive Lung Disease (GOLD) groups B, C, D (ABCD GOLD 2017 classification), and E (ABE GOLD 2023 classification) was higher in females than in males. The disease burden of female patients with COPD is higher than that of male patients in Japan, suggesting the importance of interventions considering female-dominant features such as lower absolute FVC and FEV , respiratory failure, and asthma-like conditions.

Light-absorbing particles on surface ice in ablation areas can accelerate glacier melting and shrinkage. A Single Soot Particle Photometer was used to measure black carbon (BC) mass concentrations (MBC) in the ablation area of Potanin Glacier, Mongolia during summer. Surface-ice MBC values (42–555 ng g−1) greatly exceeded those of surface snow (5–22 ng g−1), snow and rain (2–6 ng g−1), and surface melt water (2–11 ng g−1). Vertical profiles of MBC revealed high surface-layer concentrations, suggesting impurities trapped in the granular ice: the particularly low-density layer of the weathering crust surface. In the ablation area, MBC values of granular ice decreased with lower elevation: 134–601 ng g−1 at the 3317 m site and 8–96 ng g−1 at the 3078 m site. The fraction of residual surface BC to BC contained in lost water over a year, R, was calculated using the yearly BC deposition flux and water ablation weight Aw. Average R values were 0.17 and 0.011, respectively, at 3317 and 3078 m. Aw were 246 and 325 gw.e.cm-2, suggesting that the granular ice retains BC particles best in the upstream ablation area, showing concomitantly less capability with increasing ablation. Enriched BC on the ablation area surface comprises recent BC deposits and BC from the glacier's lower layer after rising during decades or more. Those BC emissions and deposits can therefore affect both future and present ablation area melting processes.

Black carbon (BC) particles in the Arctic contribute to rapid warming of the Arctic by heating the atmosphere and snow and ice surfaces. Understanding the source contributions to Arctic BC is therefore important, but they are not well understood, especially those for atmospheric and snow radiative effects. Here we estimate simultaneously the source contributions of Arctic BC to near-surface and vertically integrated atmospheric BC mass concentrations (MBC_SRF and MBC_COL), BC deposition flux (MBC_DEP), and BC radiative effects at the top of the atmosphere and snow surface (REBC_TOA and REBC_SNOW) and show that the source contributions to these five variables are highly different. In our estimates, Siberia makes the largest contribution to MBC_SRF, MBC_DEP, and REBC_SNOW in the Arctic (defined as >70∘ N), accounting for 70 %, 53 %, and 41 %, respectively. In contrast, Asia's contributions to MBC_COL and REBC_TOA are largest, accounting for 37 % and 43 %, respectively. In addition, the contributions of biomass burning sources are larger (29 %–35 %) to MBC_DEP, REBC_TOA, and REBC_SNOW, which are highest from late spring to summer, and smaller (5.9 %–17 %) to MBC_SRF and MBC_COL, whose concentrations are highest from winter to spring. These differences in source contributions to these five variables are due to seasonal variations in BC emission, transport, and removal processes and solar radiation, as well as to differences in radiative effect efficiency (radiative effect per unit BC mass) among sources. Radiative effect efficiency varies by a factor of up to 4 among sources (1471–5326 W g−1) depending on lifetimes, mixing states, and heights of BC and seasonal variations of emissions and solar radiation. As a result, source contributions to radiative effects and mass concentrations (i.e., REBC_TOA and MBC_COL, respectively) are substantially different. The results of this study demonstrate the importance of considering differences in the source contributions of Arctic BC among mass concentrations, deposition, and atmospheric and snow radiative effects for accurate understanding of Arctic BC and its climate impacts.

Aerosol particles were collected at various altitudes in the Arctic during the Polar Airborne Measurements and Arctic Regional Climate Model Simulation Project 2018 (PAMARCMiP 2018) conducted in the early spring of 2018. The composition, size, number fraction, and mixing state of individual aerosol particles were analyzed using transmission electron microscopy (TEM), and their sources and transport were evaluated by numerical model simulations. We found that sulfate, sea-salt, mineral-dust, K-bearing, and carbonaceous particles were the major aerosol constituents. Many particles were composed of two or more compositions that had coagulated and were coated with sulfate, organic materials, or both. The number fraction of mineral-dust and sea-salt particles decreased with increasing altitude. The K-bearing particles increased within a biomass burning (BB) plume at altitudes > 3900 m, which originated from Siberia. Chlorine in sea-salt particles was replaced with sulfate at high altitudes. These results suggest that the sources, transport, and aging of Arctic aerosols largely vary depending on the altitude and air-mass history. We also provide the occurrences of solid-particle inclusions (soot, fly-ash, and Fe-aggregate particles), some of which are light-absorbing particles. They were mainly emitted from anthropogenic and biomass burning sources and were embedded within other relatively large host particles. Our TEM measurements revealed the detailed mixing state of individual particles at various altitudes in the Arctic. This information facilitates the accurate evaluation of the aerosol influences on Arctic haze, radiation balance, cloud formation, and snow/ice albedo when deposited.

Aerosol composition and mixing state influence its ability to form cloud droplets and ice crystals and to scatter and absorb sunlight, all of which affect its impact on climate. In this study, aerosol samples were collected from different altitudes, ranging from the sea surface to ∼ 8000 m, over the ocean in the western North Pacific in the summer of 2022 using an aircraft and a research vessel. The samples were classified into three periods based on the sampled air parcel sources: ocean and desert (period 1), Siberian Forest biomass burning event (period 2), and their mixtures (period 3). Measurements of particle composition using transmission electron microscopy with energy-dispersive X-ray spectrometry revealed that samples from period 1 had high sea salt and mineral dust fractions, whereas samples from period 2 had high fractions of potassium-bearing particles with organics and black carbon. Samples from period 3 showed influences of both sea spray and biomass burning. During periods 1 and 3, the sea salt fractions increased as the samples were collected at lower altitudes. The compositions of biomass burning and sea spray were mixed at individual particles, with higher fractions of Na and K during period 1 and period 2, respectively, than in other periods. Our analysis of individual particles revealed a wide range of compositions and mixing states of particles, which depend on the aerosol source, size, and altitude. These factors need to be considered when evaluating aerosol composition and mixing state, both of which affect aerosol climate effects.

Vertical profiles of the mass concentration of black carbon (BC) were measured at altitudes up to 5 km during the PAMARCMiP (Polar Airborne Measurements and Arctic Regional Climate Model simulation Project) aircraft-based field experiment conducted around the northern Greenland Sea (Fram Strait) during March and April 2018 from operation base Station Nord (81.6∘ N, 16.7∘ W). Median BC mass concentrations in individual altitude ranges were 7–18 ng m−3 at standard temperature and pressure at altitudes below 4.5 km. These concentrations were systematically lower than previous observations in the Arctic in spring, conducted by ARCTAS-A in 2008 and NETCARE in 2015, and similar to those observed during HIPPO3 in 2010. Column amounts of BC for altitudes below 5 km in the Arctic (>66.5∘ N; COLBC), observed during the ARCTAS-A and NETCARE experiments, were higher by factors of 4.2 and 2.7, respectively, than those of the PAMARCMiP experiment. These differences could not be explained solely by the different locations of the experiments. The year-to-year variation of COLBC values generally corresponded to that of biomass burning activities in northern midlatitudes over western and eastern Eurasia. Furthermore, numerical model simulations estimated the year-to-year variation of contributions from anthropogenic sources to be smaller than 30 %–40 %. These results suggest that the year-to-year variation of biomass burning activities likely affected BC amounts in the Arctic troposphere in spring, at least in the years examined in this study. The year-to-year variations in BC mass concentrations were also observed at the surface at high Arctic sites Ny-Ålesund and Utqiaġvik (formerly known as Barrow, the location of Barrow Atmospheric Baseline Observatory), although their magnitudes were slightly lower than those in COLBC. Numerical model simulations in general successfully reproduced the observed COLBC values for PAMARCMiP and HIPPO3 (within a factor of 2), whereas they markedly underestimated the values for ARCTAS-A and NETCARE by factors of 3.7–5.8 and 3.3–5.0, respectively. Because anthropogenic contributions account for nearly all of the COLBC (82 %–98 %) in PAMARCMiP and HIPPO3, the good agreement between the observations and calculations for these two experiments suggests that anthropogenic contributions were generally well reproduced. However, the significant underestimations of COLBC for ARCTAS-A and NETCARE suggest that biomass burning contributions were underestimated. In this study, we also investigated plumes with enhanced BC mass concentrations, which were affected by biomass burning emissions, observed at 5 km altitude. Interestingly, the mass-averaged diameter of BC (core) and the shell-to-core diameter ratio of BC-containing particles in the plumes were generally not very different from those in other air samples, which were considered to be mostly aged anthropogenic BC. These observations provide a useful basis to evaluate numerical model simulations of the BC radiative effect in the Arctic region in spring.

Ice cores can provide long-term records of refractory black carbon (rBC), an important aerosol species closely linked to the climate and environment. However, previous studies of ice cores only analyzed rBC particles with a diameter of < 500 nm, which could have led to an underestimation of rBC mass concentrations. Information on the size distribution of rBC particles is very limited, and there are no Arctic ice core records of the temporal variation in rBC size distribution. In this study, we applied a recently developed improved technique to analyze the rBC concentration in an ice core drilled at the SIGMA-D site in northwestern Greenland. The improved technique, which uses the modified Single-Particle Soot Photometer (SP2) and a high-efficiency nebulizer, widens the measurable range of rBC particle size. For high-resolution continuous analyses of ice cores, we developed a continuous flow analysis (CFA) system. Coupling of the improved rBC measurement technique with the CFA system allows accurate high-resolution measurements of the size distribution and concentration of rBC particles with a diameter between 70 nm and 4 µm, with minimal particle losses. Using this technique, we reconstructed the size distributions and the number and mass concentrations of rBC particles during the past 350 years. On the basis of the size distributions, we assessed the underestimation of rBC mass concentrations measured using the conventional SP2s. For the period 2003–2013, the underestimation of the average mass concentration would have been 12 %–31 % for the SIGMA-D core.

The roles and impacts of refractory black carbon (rBC), an important aerosol species affecting Earth's radiation budget, are not well understood owing to a lack of accurate long-term observations. To study the temporal changes in rBC since the pre-industrial period, we analyzed rBC in an ice core drilled in northwestern Greenland. Using an improved technique for rBC measurement and a continuous flow analysis (CFA) system, we obtained accurate and high-temporal-resolution records of rBC particle size and mass/number concentrations for the past 350 years. Number and mass concentrations, which both started to increase in the 1870s associated with the inflow of anthropogenically derived rBC, reached their maxima in the 1910s–1920s and then subsequently decreased. Backward-trajectory analyses suggest that North America was likely the dominant source region of the anthropogenic rBC in the ice core. The increase in anthropogenic rBC shifted the annual concentration peaks of rBC from summer to winter–early spring. After rBC concentrations diminished to pre-industrial levels, the annual peak concentration of rBC returned to the summer. We found that anthropogenic rBC particles were larger than biomass burning rBC particles. By separating the rBC in winter and summer, we reconstructed the temporal variations in rBC that originated from biomass burning, including the period with large anthropogenic input. The rBC that originated from biomass burning showed no trend in increase until the early 2000s. Finally, possible albedo reductions due to rBC are discussed. Our new data provide key information for validating aerosol and climate models, thereby supporting improved projections of future climate and environment.

Long-term measurements of atmospheric mass concentrations of black carbon (BC) are needed to investigate changes in its emission, transport, and deposition. However, depending on instrumentation, parameters related to BC such as aerosol absorption coefficient (babs) have been measured instead. Most ground-based measurements of babs in the Arctic have been made by filter-based absorption photometers, including particle soot absorption photometers (PSAPs), continuous light absorption photometers (CLAPs), Aethalometers, and multi-angle absorption photometers (MAAPs). The measured babs can be converted to mass concentrations of BC (MBC) by assuming the value of the mass absorption cross section (MAC; MBC= babs/ MAC). However, the accuracy of conversion of babs to MBC has not been adequately assessed. Here, we introduce a systematic method for deriving MAC values from babs measured by these instruments and independently measured MBC. In this method, MBC was measured with a filter-based absorption photometer with a heated inlet (COSMOS). COSMOS-derived MBC (MBC (COSMOS)) is traceable to a rigorously calibrated single particle soot photometer (SP2), and the absolute accuracy of MBC (COSMOS) has been demonstrated previously to be about 15 % in Asia and the Arctic. The necessary conditions for application of this method are a high correlation of the measured babs with independently measured MBC and long-term stability of the regression slope, which is denoted as MACcor (MAC derived from the correlation). In general, babs–MBC (COSMOS) correlations were high (r2= 0.76–0.95 for hourly data) at Alert in Canada, Ny-Ålesund in Svalbard, Barrow (NOAA Barrow Observatory) in Alaska, Pallastunturi in Finland, and Fukue in Japan and stable for up to 10 years. We successfully estimated MACcor values (10.8–15.1 m2 g−1 at a wavelength of 550 nm for hourly data) for these instruments, and these MACcor values can be used to obtain error-constrained estimates of MBC from babs measured at these sites even in the past, when COSMOS measurements were not made. Because the absolute values of MBC at these Arctic sites estimated by this method are consistent with each other, they are applicable to the study of spatial and temporal variation in MBC in the Arctic and to evaluation of the performance of numerical model calculations.