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    Do new sea spray aerosol source functions improve the results of a regional aerosol model?
    (Amsterdam [u.a.] : Elsevier Science, 2018) Barthel, Stefan; Tegen, Ina; Wolke, Ralf
    Sea spray aerosol particle is a dominating part of the global aerosol mass load of natural origin. Thus, it strongly influences the atmospheric radiation balance and cloud properties especially over the oceans. Uncertainties of the estimated climate impacts by this aerosol type are partly caused by the uncertainties in the particle size dependent emission fluxes of sea spray aerosol particle. We present simulations with a regional aerosol transport model system in two domains, for three months and compared the model results to measurements at four stations using various sea spray aerosol particle source source functions. Despite these limitations we found the results using different source functions are within the range of most model uncertainties. Especially the model's ability to produce realistic wind speeds is crucial. Furthermore, the model results are more affected by a function correcting the emission flux for the effect of the sea surface temperature than by the use of different source functions. © 2018 The Authors
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    Marine organic matter in the remote environment of the Cape Verde islands-an introduction and overview to the MarParCloud campaign
    (Katlenburg-Lindau : EGU, 2020) van Pinxteren, Manuela; Fomba, KhannehWadinga; Triesch, Nadja; Stolle, Christian; Wurl, Oliver; Bahlmann, Enno; Gong, Xianda; Voigtländer, Jens; Wex, Heike; Robinson, Tiera-Brandy; Barthel, Stefan; Zeppenfeld, Sebastian; Hoffmann, Erik Hans; Roveretto, Marie; Li, Chunlin; Grosselin, Benoit; Daële, Veronique; Senf, Fabian; van Pinxteren, Dominik; Manzi, Malena; Zabalegui, Nicolás; Frka, Sanja; Gašparović, Blaženka; Pereira, Ryan; Li, Tao; Wen, Liang; Li, Jiarong; Zhu, Chao; Chen, Hui; Chen, Jianmin; Fiedler, Björn; von Tümpling, Wolf; Read, Katie Alana; Punjabi, Shalini; Lewis, Alastair Charles; Hopkins, James Roland; Carpenter, Lucy Jane; Peeken, Ilka; Rixen, Tim; Schulz-Bull, Detlef; Mong, María Eugenia; Mellouki, Abdelwahid; George, Christian; Stratmann, Frank; Herrmann, Hartmut
    The project MarParCloud (Marine biological production, organic aerosol Particles and marine Clouds: a process chain) aims to improve our understanding of the genesis, modification and impact of marine organic matter (OM) from its biological production, to its export to marine aerosol particles and, finally, to its ability to act as ice-nucleating particles (INPs) and cloud condensation nuclei (CCN). A field campaign at the Cape Verde Atmospheric Observatory (CVAO) in the tropics in September-October 2017 formed the core of this project that was jointly performed with the project MARSU (MARine atmospheric Science Unravelled). A suite of chemical, physical, biological and meteorological techniques was applied, and comprehensive measurements of bulk water, the sea surface microlayer (SML), cloud water and ambient aerosol particles collected at a ground-based and a mountain station took place. Key variables comprised the chemical characterization of the atmospherically relevant OM components in the ocean and the atmosphere as well as measurements of INPs and CCN. Moreover, bacterial cell counts, mercury species and trace gases were analyzed. To interpret the results, the measurements were accompanied by various auxiliary parameters such as air mass back-trajectory analysis, vertical atmospheric profile analysis, cloud observations and pigment measurements in seawater. Additional modeling studies supported the experimental analysis. During the campaign, the CVAO exhibited marine air masses with low and partly moderate dust influences. The marine boundary layer was well mixed as indicated by an almost uniform particle number size distribution within the boundary layer. Lipid biomarkers were present in the aerosol particles in typical concentrations of marine background conditions. Accumulation-and coarse-mode particles served as CCN and were efficiently transferred to the cloud water. The ascent of ocean-derived compounds, such as sea salt and sugar-like compounds, to the cloud level, as derived from chemical analysis and atmospheric transfer modeling results, denotes an influence of marine emissions on cloud formation. Organic nitrogen compounds (free amino acids) were enriched by several orders of magnitude in submicron aerosol particles and in cloud water compared to seawater. However, INP measurements also indicated a significant contribution of other non-marine sources to the local INP concentration, as (biologically active) INPs were mainly present in supermicron aerosol particles that are not suggested to undergo strong enrichment during ocean-atmosphere transfer. In addition, the number of CCN at the supersaturation of 0.30 % was about 2.5 times higher during dust periods compared to marine periods. Lipids, sugar-like compounds, UV-absorbing (UV: ultraviolet) humic-like substances and low-molecularweight neutral components were important organic compounds in the seawater, and highly surface-active lipids were enriched within the SML. The selective enrichment of specific organic compounds in the SML needs to be studied in further detail and implemented in an OM source function for emission modeling to better understand transfer patterns, the mechanisms of marine OM transformation in the atmosphere and the role of additional sources. In summary, when looking at particulate mass, we see oceanic compounds transferred to the atmospheric aerosol and to the cloud level, while from a perspective of particle number concentrations, sea spray aerosol (i.e., primary marine aerosol) contributions to both CCN and INPs are rather limited. © Author(s) 2020.
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    An overview of the ACE-2 clear sky column closure experiment (CLEARCOLUMN)
    (Milton Park : Taylor & Francis, 2016) Russell, Philip B.; Heintzenberg, Jost
    As 1 of 6 focused ACE-2 activities, a clear sky column closure experiment (CLEARCOLUMN) took place in June/July 1997 at the southwest corner of Portugal, in the Canary Islands, and over the eastern Atlantic Ocean surrounding and linking those sites. Overdetermined sets of volumetric, vertical profile and columnar aerosol data were taken from the sea surface to~5 km asl by samplers and sensors at land sites (20–3570 m asl), on a ship, and on 4 aircraft. In addition, 5 satellites measured upwelling radiances used to derive properties of the aerosol column. Measurements were made in a wide range of conditions and locations (e.g., the marine boundary layer with and without continental pollution, the free troposphere with and without African dust). Numerous tests of local and column closure, using unidisciplinary and multidisciplinary approaches, were conducted. This paper summarizes the methodological approach, the experiment sites and platforms, the types of measurements made on each, the types of analyses conducted, and selected key results, as a guide to the more complete results presented in other papers in this special issue and elsewhere. Example results include determinations of aerosol single scattering albedo by several techniques, measurements of hygroscopic effects on particle light scattering and size, and a wide range in the degree of agreement found in closure tests. In general, the smallest discrepancies were found in comparisons among (1) different techniques to measure an optical property of the ambient, unperturbed aerosol (e.g., optical depth, extinction, or backscatter by sunphotometer, lidar, and/or satellite) or (2) different techniques to measure an aerosol that had passed through a common sampling process (e.g., nephelometer and size spectrometer measurements with the same or similar inlets, humidities and temperatures). Typically, larger discrepancies were found between techniques that measure the ambient, unperturbed aerosol and those that must reconstruct the ambient aerosol by accounting for (a) processes that occur during sampling (e.g., aerodynamic selection, evaporation of water and other volatile material) or ( b) calibrations that depend on aerosol characteristics (e.g., sizedependent density or refractive index). A primary reason for the discrepancies in such cases is the lack of validated hygroscopic growth models covering the necessary range of particle sizes and compositions. Other common reasons include (1) using analysis or retrieval techniques that assume aerosol properties (e.g., density, single scattering albedo, shape) that do not apply in all cases and (2) using surface measurements to estimate column properties. Taken together, the ACE-2 CLEARCOLUMN data set provides a large collection of new information on the properties of the aerosol over the northeast Atlantic Ocean. CLEARCOLUMN studies have also pointed to improved techniques for analyzing current and future data sets (including satellite data sets) which will provide a more accurate and comprehensive description of the Atlantic–European–African aerosol. Thus they set the stage for an improved regional quantification of radiative forcing by anthropogenic aerosols.