Size distribution and chemical composition of marine aerosols: A compilation and review

Some 30 years of physical and chemical marine aerosol data are reviewed to derive global-size distribution parameters and inorganic particle composition on a coarse 15°×15° grid. There are large gaps in geographical and seasonal coverage and chemical and physical aerosol characterisation. About 28% of the grid cells contain physical data while there are compositional data in some 60% of the cells. The size distribution data were parametrized in terms of 2 submicrometer log-normal distributions. The sparseness of the data did not allow zonal differentiation of the distributions. By segregating the chemical data according to the major aerosol sources, sea salt, dimethylsulfide, crustal material, combustion processes and other anthropogenic sources, much information on mass concentrations and contribution of natural and anthropogenic sources to the marine aerosol can be gleaned from the data base. There are significant meridional differences in the contributions of the different sources to the marine aerosol. Very clearly, we see though that the global marine surface atmosphere is polluted by anthropogenic sulfur. Only in the case of sulfur components did the coverage allow the presentation of very coarse seasonal distributions which reflect the spring blooms in the appropriate parts of the oceans. As an example of the potential value in comparing the marine aerosol data base to chemical transport models, global seasonal meridional MSA distributions were compared to modelled MSA distributions. The general good agreement in mass concentrations is encouraging while some latitudinal discrepancies warrant further investigations covering other aerosol components such as black carbon and metals

Marginal Damage of Methane Emissions: Ozone Impacts on Agriculture

Methane directly contributes to air pollution, as an ozone precursor, and to climate change, generating physical and economic damages to different systems, namely agriculture, vegetation, energy, human health, or biodiversity. The methane-related damages to climate, measured as the Social Cost of Methane, and to human health have been analyzed by different studies and considered by government rulemaking in the last decades, but the ozone-related damages to crop revenues associated to methane emissions have not been incorporated to policy agenda. Using a combination of the Global Change Analysis Model and the TM5-FASST Scenario Screening Tool, we estimate that global marginal agricultural damages range from ~ 423 to 556 $2010/t-CH4, of which 98$2010/t-CH4 occur in the USA, which is the most affected region due to its role as a major crop producer, followed by China, EU-15, and India. These damages would represent 39–59% of the climate damages and 28–64% of the human health damages associated with methane emissions by previous studies. The marginal damages to crop revenues calculated in this study complement the damages from methane to climate and human health, and provides valuable information to be considered in future cost-benefits analyses. © 2023, The Author(s).JS and SW were supported by the U.S. Environmental Protection Agency, under Interagency Agreement DW-089-92459801. The views expressed in this article are purely those of the authors and do not, under any circumstances, represent the views or policies of the U.S. Environmental Protection Agency or the European Commission. JS and SW were supported by the U.S. Environmental Protection Agency, under Interagency Agreement DW-089-92459801. The views expressed in this article are purely those of the authors and do not, under any circumstances, represent the views or policies of the U.S. Environmental Protection Agency or the European Commission

LC-MS analysis of aerosol particles from the oxidation of ?-pinene by ozone and OH-radicals

International audienceThe time resolved chemical composition of aerosol particles, formed by the oxidation of alpha-pinene has been investigated by liquid chromatography/mass spectrometry (LC-MS) using negative and positive ionisation methods (ESI(-) and APCI(+)). The experiments were performed at the EUPHORE facility in Valencia (Spain) under various experimental conditions, including dark ozone reactions, photosmog experiments with low NOx mixing ratios and reaction with OH radicals in the absence of NOx (H2O2-photolysis). Particles were sampled on PTFE f ilters at different stages of the reaction and extracted with methanol. The predominant products from alpha-pinene in the particulate phase are cis-pinic acid, cis-pinonic acid and hydroxy-pinonic acid isomers. Another major compound with molecular weight 172 was detected, possibly a hydroxy-carboxylic acid. These major compounds account for 50% to 80% of the identified aerosol products, depending on the time of sampling and type of experiment. In addition, more than 20 different products have been detected and structures have been tentatively assigned based on their molecular weight and responses to the different ionisation modes. The different experiments performed showed that the aerosol formation is mainly caused by the ozonolysis reaction. The highest aerosol yields were observed in the dark ozone experiments, for which also the highest ratios of mass of identified products to the formed aerosol mass were found (30% to 50%, assuming a density of 1 g cm-3)

Physical aerosol properties and their relation to air mass origin at Monte Cimone (Italy) during the first MINATROC campaign

Aerosol physical properties were measured at the Monte Cimone Observatory (Italy) from 1 June till 6 July 2000. The measurement site is located in the transition zone between the continental boundary layer and the free troposphere (FT), at the border between the Mediterranean area and Central Europe, and is exposed to a variety of air masses. Sub-&mu;m number size distributions, aerosol hygroscopicity near 90% RH, refractory size distribution at 270&deg;C and equivalent black carbon mass were continuously measured. Number size distributions and hygroscopic properties indicate that the site is exposed to aged continental air masses, however during daytime it is also affected by upslope winds. The mixing of this transported polluted boundary layer air masses with relatively clean FT air leads to frequent nucleation events around local noon. <P style='line-height: 20px;'> Night-time size distributions, including fine and coarse fractions for each air mass episode, have been parameterized by a 3-modal lognormal distribution. Number and volume concentrations in the sub-&mu;m modes are strongly affected by the air mass origin, with highest levels in NW-European air masses, versus very clean, free tropospheric air coming from the N-European sector. During a brief but distinct dust episode, the coarse mode is clearly enhanced. <P style='line-height: 20px;'> The observed hygroscopic behavior of the aerosol is consistent with the chemical composition described by Putaud et al.&nbsp;(2004), but no closure between known chemical composition and measured hygroscopicity could be made because the hygroscopic properties of the water-soluble organic matter (WSOM) are not known. The data suggest that WSOM is slightly-to-moderately hygroscopic (hygroscopic growth factor GF at 90% relative humidity between 1.05 and 1.51), and that this property may well depend on the air mass origin and history. <P style='line-height: 20px;'> External mixing of aerosol particles is observed in all air masses through the occurrence of two hygroscopicity modes (average GF of 1.22 and 1.37, respectively). However, the presence of 'less' hygroscopic particles has mostly such a low occurrence rate that the average growth factor distribution for each air mass sector actually appears as a single mode. This is not the case for the dust episode, where the external mixing between less hygroscopic and more hygroscopic particles is very prominent, and indicating clearly the occurrence of a dust accumulation mode, extending down to 50 nm particles, along with an anthropogenic pollution mode. <P style='line-height: 20px;'> The presented physical measurements finally allow us to provide a partitioning of the sub-&mu;m aerosol in four non-overlapping fractions (soluble/volatile, non-soluble/volatile, refractory/non-black carbon, black carbon) which can be associated with separate groups of chemical compounds determined with chemical-analytical techniques (ions, non-water soluble organic matter, dust, elemental carbon). All air masses except the free-tropospheric N-European and Dust episodes show a similar composition within the uncertainty of the data (53%, 37%, 5% and 5% respectively for the four defined fractions). Compared to these sectors, the dust episode shows a clearly enhanced refractory-non-BC fraction (17%), attributed to dust in the accumulation mode, whereas for the very clean N-EUR sector, the total refractory fraction is 25%, of which 13% non-BC and 12% BC

Co-benefits of black carbon mitigation for climate and air quality

Mitigation of black carbon (BC) aerosol emissions can potentially contribute to both reducing air pollution and climate change, although mixed results have been reported regarding the latter. A detailed quantification of the synergy between global air quality and climate policy is still lacking. This study contributes with an integrated assessment model-based scenario analysis of BC-focused mitigation strategies aimed at maximizing air quality and climate benefits. The impacts of these policy strategies have been examined under different socio-economic conditions, climate ambitions, and BC mitigation strategies. The study finds that measures targeting BC emissions (including reduction of co-emitted organic carbon, sulfur dioxide, and nitrogen dioxides) result in significant decline in premature mortality due to ambient air pollution, in the order of 4 to 12 million avoided deaths between 2015 and 2030. Under certain circumstances, BC mitigation can also reduce climate change, i.e., mainly by lowering BC emissions in the residential sector and in high BC emission scenarios. Still, the effect of BC mitigation on global mean temperature is found to be modest at best (with a maximum short-term GMT decrease of 0.02 °C in 2030) and could even lead to warming (with a maximum increase of 0.05 °C in case of a health-focused strategy, where all aerosols are strongly reduced). At the same time, strong climate policy would improve air quality (the opposite relation) through reduced fossil fuel use, leading to an estimated 2 to 5 million avoided deaths in the period up to2030. By combining both air quality and climate goals, net health benefits can be maximized

Actuariële bedenkingen bij een eenvormig opgelegd bonus-malus stelsel.

Verscheidene actoren van het verzekeringswezen dringen sterk aan om het verplicht eenvormig bonus-malus stelsel in de verzekering B.A.-auto te behouden. In deze nota wordt aan de hand van een theoretisch voorbeeld aangetoond dat dit standpunt vanuit actuariëel oogpunt onhoudbaar is.

Threats for Global Food Supply of Increasing Surface Ozone - Spatial Assessment of Impacts and Adaptation Options

Surface ozone (O3) is a potent phytotoxic air pollutant and significantly reduces the productivity of important agricultural crops. Growing use of fossil fuel and changes in climate are increasing the global background surface ozone concentrations to levels that threaten regional and global food supply. We performed an integrated modeling study, considering biophysical and crop management factors, to identify the spatial pattern of ozone damage in lands suitable for crop cultivation and to assess the potential for adaptation for four key crops (wheat, maize, rice and soybean) under current and future air quality legislation. Results indicate that China, India and the United States are by far the most affected countries, bearing more than half of all global losses and threatened areas. Short-erm adaptive measures at farm level, such as shifting crop calendars (by changing sowing dates or using crop cultivars with different cycle lengths) can reduce ozone damage regionally but have only limited impact at the global level. Considering these limited benefits of adaptation, mitigation of O3 precursors remains the main option to secure regional and global food production

Lidar and in situ observations of continental and Saharan aerosol: closure analysis of particles optical and physical properties

Single wavelength polarization lidar observations collected at Mt. Cimone (44.2º N, 10.7º E, 1870 m a.s.l.) during the June 2000 MINATROC campaign are analyzed to derive tropospheric profiles of aerosol extinction, depolarization, surface area and volume. Lidar retrievals for the 2170-2245 m level are compared to the same variables as computed from in situ measurements of particles size distributions, performed at the mountain top Station (2165 m a.s.l.) by a differential mobility analyzer (DMA) and an optical particle counter (OPC). A sensitivity analysis of this closure experiment shows that mean relative differences between the backscatter coefficients obtained by the two techniques undergo a sharp decrease when hygroscopic growth to ambient humidity is considered for the DMA dataset, otherwise representative of dry aerosols. Minimization of differences between lidar and size distribution-derived backscatter coefficients allowed to find values of the &quot;best&quot; refractive index, specific to each measurement. These results show the refractive index to increase for air masses proceeding from Africa and Western Europe. Lidar depolarization was observed to minimize mainly in airmasses proceeding from Western Europe, thus indicating a spherical, i.e. liquid nature for such aerosols. Conversely, African, Mediterranean and East Europe aerosol showed a larger depolarizing fraction, mainly due to coexisting refractory and soluble fractions. The analysis shows average relative differences between lidar and in-situ observations of 5% for backscatter, 36% for extinction 41% for surface area and 37% for volume. These values are well within the expected combined uncertainties of the lidar and in situ retrievals. Average differences further decrease during the Saharan dust transport event, when a lidar signal inversion model considering non-spherical scatterers is employed. The quality of the closure obtained between particle counter and lidar-derived aerosol surface area and volume observations constitutes a validation of the technique adopted to retrieve such aerosol properties on the basis of single-wavelength lidar observations