250 results match your criteria: "Institute for Tropospheric Research[Affiliation]"

Gas-Phase Formation of Sulfurous Acid (HSO) in the Atmosphere.

Angew Chem Int Ed Engl

July 2024

Atmospheric Chemistry Department (ACD), Leibniz Institute for Tropospheric Research (TROPOS), Permoserstraße 15, 04318, Leipzig, Germany.

Sulfurous acid (HSO) is known to be thermodynamically instable decomposing into SO and HO. All attempts to detect this elusive acid in solution failed up to now. Reported HSO formation from an experiment carried out in a mass spectrometer as well as results from theoretical calculations, however, indicated a possible kinetic stability in the gas phase.

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Although desert dust promotes morbidity and mortality, it is exempt from regulations. Its health effects have been related to its inflammatory properties, which can vary between source regions. It remains unclear which constituents cause this variability.

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Particulate matter (PM) is an important component in the atmosphere, affecting air quality, health, radiation balance, and global climate. To assess regional air quality in the city of Fez, an intensive field campaign was carried out in the autumn of 2019 in the Middle Atlas region of Morocco. Aerosol sampling was performed simultaneously at two urban sites in the city of Fez: (1) Fez University (FU), a sub-urban site, and (2) Fez Parc (FP), an urban site located in the city center of Fez, using PM collectors.

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Ultrafine particles (UFP, those with diameters ≤ 100 nm), have been reported to potentially penetrate deeply into the respiratory system, translocate through the alveoli, and affect various organs, potentially correlating with increased mortality. The aim of this study is to assess long-term trends (5-11 years) in mostly urban UFP concentrations based on measurements of particle number size distributions (PNSD). Additionally, concentrations of other pollutants and meteorological variables were evaluated to support the interpretations.

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Article Synopsis
  • This study focuses on how to accurately measure equivalent black carbon (eBC) concentrations using filter absorption photometers (FAPs) by understanding the mass absorption cross-section (MAC).
  • Researchers analyzed data from 22 different sites to compare various methods for calculating MAC, leading to different classifications of eBC such as LeBC, MeBC, and ReBC, with significant differences observed in measurement outcomes.
  • Results showed that MAC varies by site and season, influencing the observed trends in elemental carbon (EC), revealing a need for careful MAC consideration when interpreting eBC data to reduce uncertainty in measurements.
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Risk assessment of pesticide impacts on remote ecosystems makes use of model-estimated degradation in air. Recent studies suggest these degradation rates to be overestimated, questioning current pesticide regulation. Here, we investigated the concentrations of 76 pesticides in Europe at 29 rural, coastal, mountain, and polar sites during the agricultural application season.

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Residential wood combustion contributing to airborne particulate matter (PM) was studied for 1 year at two sites in the village of Melpitz. Significant excess pollution was observed at the Melpitz center compared to that at the TROPOS research station Melpitz reference site, situated only 700 m away. Local concentration increments at the village site for the combustion PM constituents organic carbon, elemental carbon, levoglucosan, and benzo[a]pyrene were determined under appropriate wind directions, and their winter mean values were 0.

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Highly oxygenated organic molecules (HOMs) are a major source of new particles that affect the Earth's climate. HOM production from the oxidation of volatile organic compounds (VOCs) occurs during both the day and night and can lead to new particle formation (NPF). However, NPF involving organic vapors has been reported much more often during the daytime than during nighttime.

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This paper presents the study design of the Berlin-Brandenburg Air study (BEAR-study). We measure air quality in Berlin and Brandenburg before and after the relocation of aircraft (AC) traffic from Tegel (TXL) airport to the new Berlin-Brandenburg airport (BER) and investigate the association of AC-related ultrafine particles (UFP) with health outcomes in schoolchildren. The BEAR-study is a natural experiment examining schoolchildren attending schools near TXL and BER airports, and in control areas (CA) away from both airports and associated air corridors.

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Factors Influencing the Formation of Nitrous Acid from Photolysis of Particulate Nitrate.

J Phys Chem A

November 2023

Wolfson Atmospheric Chemistry Laboratories, Department of Chemistry, University of York, York YO10 5DD, U.K.

Enhanced photolysis of particulate nitrate (pNO) to form photolabile species, such as gas-phase nitrous acid (HONO), has been proposed as a potential mechanism to recycle nitrogen oxides (NO) in the remote boundary layer ("renoxification"). This article presents a series of laboratory experiments aimed at investigating the parameters that control the photolysis of pNO and the efficiency of HONO production. Filters on which artificial or ambient particles had been sampled were exposed to the light of a solar simulator, and the formation of HONO was monitored under controlled laboratory conditions.

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Background: Epidemiological studies have related desert dust events to increased respiratory morbidity and mortality. Although the Sahara is the largest source of desert dust, Saharan dust (SD) has been barely examined in toxicological studies. Here, we aimed to assess the NLRP3 inflammasome-caspase-1-pathway-dependent pro-inflammatory potency of SD in comparison to crystalline silica (DQ12 quartz) in an advanced air-liquid interface (ALI) co-culture model.

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During the Multidisciplinary Drifting Observatory for the Study of Arctic Climate expedition, a tethered balloon system was operated with a turbulence probe attached to study the lower troposphere in the high Arctic. Overall, measurements were conducted on 34 days between December 2019 and May 2020, resulting in 47 quality-assured sampling records consisting of vertical profiles and constant-altitude measurements. The continuous profiles extend from the surface, i.

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Apportioning Atmospheric Ammonia Sources across Spatial and Seasonal Scales by Their Isotopic Fingerprint.

Environ Sci Technol

October 2023

Sino-French Research Institute for Ecology and Environment, School of Environmental Science and Engineering, Shandong University, Qingdao 266237, China.

Mitigating ammonia (NH) emissions is a significant challenge, given its well-recognized role in the troposphere, contributing to secondary particle formation and impacting acid rain. The difficulty arises from the highly uncertain attribution of atmospheric NH to specific emission sources, especially when accounting for diverse environments and varying spatial and temporal scales. In this study, we established a refined δN fingerprint for eight emission sources, including three previously overlooked sources of potential importance.

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Measurements of aerosol microphysical and chemical properties in the central Arctic atmosphere during MOSAiC.

Sci Data

October 2023

Extreme Environments Research Laboratory, École Polytechnique Fédérale de Lausanne (EPFL) Valais Wallis, Sion, Switzerland.

The Arctic environment is transforming rapidly due to climate change. Aerosols' abundance and physicochemical characteristics play a crucial, yet uncertain, role in these changes due to their influence on the surface energy budget through direct interaction with solar radiation and indirectly via cloud formation. Importantly, Arctic aerosol properties are also changing in response to climate change.

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Marine viruses disperse bidirectionally along the natural water cycle.

Nat Commun

October 2023

Group for Aquatic Microbial Ecology, Department of Chemistry, Environmental Microbiology and Biotechnology (EMB), University of Duisburg-Essen, 45141, Essen, Germany.

Article Synopsis
  • Marine viruses prevalent in seawater have been less studied regarding their movement from ocean surfaces to the atmosphere.
  • A study found that 6.2% of viruses could be found in both the air-sea interface and rainwater, indicating selective enrichment and transfer of viruses, particularly from the surface microlayer and sea foams to the atmosphere.
  • The presence of specific CRISPR matches suggests frequent interactions between marine prokaryotes and foreign viruses, supporting the idea that viruses can spread through the natural water cycle.
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Dynamic evaluation of modeled ozone concentrations in Germany with four chemistry transport models.

Sci Total Environ

January 2024

FUB, Institute of Meteorology, Freie Universität Berlin, Carl-Heinrich-Becker-Weg 6-10, 12165 Berlin, Germany; RIFS Potsdam, Research Institute for Sustainability, Helmholtz Zentrum Potsdam, Berlinerstraße 130, 14467 Potsdam, Germany.

Simulating the ozone variability at regional scales using chemistry transport models (CTMs) remains a challenge. We designed a multi-model intercomparison to evaluate, for the first time, four regional CTMs on a national scale for Germany. Simulations were conducted with LOTOS-EUROS, REM-CALGRID, COSMO-MUSCAT and WRF-Chem for January 1 to December 31, 2019, using prescribed emission information.

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Highly Efficient Autoxidation of Triethylamine.

J Phys Chem A

October 2023

Department of Chemistry, University of Copenhagen, Universitetsparken 5, DK-2100 Copenhagen Ø, Denmark.

Autoxidation has been acknowledged as a major oxidation pathway in a broad range of atmospherically important compounds including isoprene and monoterpenes. More recently, autoxidation has also been identified as central and even dominant in the atmospheric oxidation of the rather small nonhydrocarbons dimethyl sulfide (DMS) and trimethylamine (TMA). Here, we find even faster autoxidation in the aliphatic amine triethylamine (TEA).

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The climate effects of atmospheric aerosol particles serving as cloud condensation nuclei (CCN) depend on chemical composition and hygroscopicity, which are highly variable on spatial and temporal scales. Here we present global CCN measurements, covering diverse environments from pristine to highly polluted conditions. We show that the effective aerosol hygroscopicity, κ, can be derived accurately from the fine aerosol mass fractions of organic particulate matter (ϵ) and inorganic ions (ϵ) through a linear combination, κ = ϵ ⋅ κ + ϵ ⋅ κ.

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Cloud condensation nuclei activity of internally mixed particle populations at a remote marine free troposphere site in the North Atlantic Ocean.

Sci Total Environ

December 2023

Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory (PNNL), Richland, WA 99352, USA. Electronic address:

This study reports results from research conducted at the Observatory of Mount Pico (OMP), 2225 m above mean sea level on Pico Island in the Azores archipelago in June and July 2017. We investigated the chemical composition, mixing state, and cloud condensation nuclei (CCN) activities of long-range transported free tropospheric (FT) particles. FLEXible PARTicle Lagrangian particle dispersion model (FLEXPART) simulations reveal that most air masses that arrived at the OMP during the sampling period originated in North America and were highly aged (average plume age > 10 days).

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Unveiling the underestimated direct emissions of nitrous acid (HONO).

Proc Natl Acad Sci U S A

August 2023

Sino-French Research Institute for Ecology and Environment, School of Environmental Science and Engineering, Shandong University, Qingdao 266237, China.

Gaseous nitrous acid (HONO) is a critical source of hydroxyl radicals (OH) in the troposphere. While both direct and secondary sources contribute to atmospheric HONO, direct emissions have traditionally been considered minor contributors. In this study, we developed δN and δO isotopic fingerprints to identify six direct HONO emission sources and conducted a 1-y case study on the isotopic composition of atmospheric HONO at rural and urban sites.

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During the Multidisciplinary drifting Observatory for the Study of Arctic Climate (MOSAiC) expedition, the Balloon-bornE moduLar Utility for profilinG the lower Atmosphere (BELUGA) was deployed from an ice floe drifting in the Fram Strait from 29 June to 27 July 2020. The BELUGA observations aimed to characterize the cloudy Arctic atmospheric boundary layer above the sea ice using a modular setup of five instrument packages. The in situ measurements included atmospheric thermodynamic and dynamic state parameters (air temperature, humidity, pressure, and three-dimensional wind), broadband solar and terrestrial irradiance, aerosol particle microphysical properties, and cloud particle images.

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Sulfuric acid represents a fundamental precursor for new nanometre-sized atmospheric aerosol particles. These particles, after subsequent growth, may influence Earth´s radiative forcing directly, or indirectly through affecting the microphysical and radiative properties of clouds. Currently considered formation routes yielding sulfuric acid in the atmosphere are the gas-phase oxidation of SO initiated by OH radicals and by Criegee intermediates, the latter being of little relevance.

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Sulfite auto-oxidation catalyzed by cobalt complexed with ammonia deposited on silica (CoNSi) was used to generate sulfate radicals. The material was characterized by ATR-FTIR, suggesting that the silica structure did not change, and SEM-EDS, indicating an uniform dispersion of cobalt across the material surface according with XRD results. BET analysis provided information on a mesoporous material (type IV isotherm) with regular morphology (H1 hysteresis).

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-dependent aqueous-phase rate constants were determined for the oxidation of the hydroxy aldehydes, glyceraldehyde, glycolaldehyde, and lactaldehyde, by the hydroxyl radicals (OH), the sulfate radicals (SO), and the nitrate radicals (NO). The obtained Arrhenius expressions for the oxidation by the OH radical are: = (3.3 ± 0.

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Halogen atoms are important atmospheric oxidants that have unidentified daytime sources from photochemical halide oxidation in sea salt aerosols. Here, we show that the photolysis of nitrate in aqueous chloride solutions generates nitryl chloride (ClNO) in addition to Cl and HOCl. Experimental and modeling evidence suggests that O(P) formed in the minor photolysis channel from nitrate oxidizes chloride to Cl and HOCl, which reacts with nitrite to form ClNO.

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