Please use this identifier to cite or link to this item: http://hdl.handle.net/2122/10589
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dc.date.accessioned2017-08-17T06:01:04Zen
dc.date.available2017-08-17T06:01:04Zen
dc.date.issued2016-
dc.identifier.urihttp://hdl.handle.net/2122/10589en
dc.description.abstractThis study examines the relationships linking methanesulfonic acid (MSA, arising from the atmospheric oxidation of the biogenic dimethylsulfide, DMS) in atmospheric aerosol, satellite-derived chlorophyll a (Chl-a), and oceanic primary production (PP), also as a function of sea ice melting (SIM) and extension of the ice free area in the marginal ice zone (IF-MIZ) in the Arctic. MSA was determined in PM10 samples collected over the period 2010–2012 at two Arctic sites, Ny Ålesund (78.9°N, 11.9°E), Svalbard islands, and Thule Air Base (76.5°N, 68.8°W), Greenland. PP is calculated by means of a bio-optical, physiologically based, semi-analytical model in the potential source areas located in the surrounding oceanic regions (Barents and Greenland Seas for Ny Ålesund, and Baffin Bay for Thule). Chl-a peaks in May in the Barents sea and in the Baffin Bay, and has maxima in June in the Greenland sea; PP follows the same seasonal pattern of Chl-a, although the differences in absolute values of PP in the three seas during the blooms are less marked than for Chl-a. MSA shows a better correlation with PP than with Chl-a, besides, the source intensity (expressed by PP) is able to explain more than 30% of the MSA variability at the two sites; the other factors explaining the MSA variability are taxonomic differences in the phytoplanktonic assemblages, and transport processes from the DMS source areas to the sampling sites. The taxonomic differences are also evident from the slopes of the correlation plots between MSA and PP: similar slopes (in the range 34.2–36.2 ng m−3of MSA/(gC m−2 d−1)) are found for the correlation between MSA at Ny Ålesund and PP in Barents Sea, and between MSA at Thule and PP in the Baffin Bay; conversely, the slope of the correlation between MSA at Ny Ålesund and PP in the Greenland Sea in summer is smaller (16.7 ng m−3of MSA/(gC m−2 d−1)). This is due to the fact that DMS emission from the Barents Sea and Baffin Bay is mainly related to the MIZ diatoms, which are prolific DMS producers, whereas in the Greenland Sea the DMS peak is related to an offshore pelagic bloom where low-DMS producer species are present. The sea ice dynamic plays a key role in determining MSA concentration in the Arctic, and a good correlation between MSA and SIM (slope = 39 ng m−3 of MSA/106 km2 SIM) and between MSA and IF-MIZ (slope = 56 ng m−3 of MSA/106 km2 IF-MIZ) is found for the cases attributable to bloomings of diatoms in the MIZ. Such relationships are calculated by combining the data sets from the two sites and suggest that PP is related to sea ice melting and to the extension of marginal sea ice areas, and that these factors are the main drivers for MSA concentrations at the considered Arctic sites.en_US
dc.description.sponsorshipPRIN 2007 2007L8Y4NB (‘‘Dirigibile Italia’’), PRIN 2009 20092C7KRC (“Arctica”), Italian Antarctic Programme (PNRA) Projects 2009/A3.04 and 2013/C3.03, Progetto Premiale ARCA.en_US
dc.language.isoEnglishen_US
dc.relation.ispartofAtmospheric environmenten_US
dc.relation.ispartofseries/136 (2016)en_US
dc.subjectbiogenic aerosolen_US
dc.subjectArcticen_US
dc.subjectsea iceen_US
dc.titleRelationships linking primary production, sea ice melting, and biogenic aerosol in the Arcticen_US
dc.typearticleen_US
dc.description.statusPublisheden_US
dc.type.QualityControlPeer-revieweden_US
dc.description.pagenumber1-15en_US
dc.subject.INGV01.01. Atmosphereen_US
dc.identifier.doi10.1016/j.atmosenv.2016.04.002en_US
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Liang Linking Phytoplankton Activity in Polynyas and Sulfur Aerosols over Zhongshan Station, East Antarctica J. Atmos. Sci, 72 (2015), pp. 4629-4642, 10.1175/JAS-D-15-0094.1 Zhuang et al., 2011 G. Zhuang, G. Yang, J. Yu, Y. Gao Production of DMS and DMSP in different physiological stages and salinity conditions in two marine algae Chin. J. Oceanogr. Limnol., 29 (2) (2011), pp. 369-377en_US
dc.description.obiettivoSpecifico5A. Ricerche polari e paleoclimaen_US
dc.description.journalTypeJCR Journalen_US
dc.contributor.authorBecagli, S.-
dc.contributor.authorLazzara, L.-
dc.contributor.authorMarchese, C.-
dc.contributor.authorDayan, U.-
dc.contributor.authorAscanius, S.E.-
dc.contributor.authorCacciani, M.-
dc.contributor.authorCaiazzo, L.-
dc.contributor.authorDi Biagio, C.-
dc.contributor.authorDi Iorio, T.-
dc.contributor.authordi Sarra, A.-
dc.contributor.authorEriksen, P.-
dc.contributor.authorFani, F.-
dc.contributor.authorGiardi, F.-
dc.contributor.authorMeloni, D.-
dc.contributor.authorMuscari, G.-
dc.contributor.authorPace, G.-
dc.contributor.authorSeveri, M.-
dc.contributor.authorTraversi, R.-
dc.contributor.authorUdisti, R.-
dc.contributor.departmentDepartment of Chemistry, University of Florenceen_US
dc.contributor.departmentIstituto Nazionale di Geofisica e Vulcanologia (INGV), Sezione Roma2, Roma, Italiaen_US
item.openairetypearticle-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.grantfulltextrestricted-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
crisitem.author.deptDepartment of Chemistry, University of Florence-
crisitem.author.deptDepartment of Biology, University of Florence-
crisitem.author.deptDépartement de Biologie, Chimie et Géographie, Université du Québec à Rimouski, Rimousk-
crisitem.author.deptDanish Meteorological Institute, Qanaaq, Greenland-
crisitem.author.deptDipartimeno di Fisica, Università di Roma «La Sapienza», Roma, Italy-
crisitem.author.deptDepartment of Chemistry, University of Florence-
crisitem.author.deptENEA/UTMEA-TER, S. Maria di Galeria, Italy-
crisitem.author.deptENEA, Laboratory for Observations and Analyses of Earth and Climate-
crisitem.author.deptDanish Meteorological Institute, Copenhagen, Denmark-
crisitem.author.deptIstituto Nazionale di Geofisica e Vulcanologia (INGV), Sezione Roma2, Roma, Italia-
crisitem.author.deptUniversità degli Studi di Roma «La Sapienza», Roma, Italy-
crisitem.author.deptDipartimento di Chimica, University of Florence, Florence, Italy-
crisitem.author.deptDipartimento di Chimica, University of Florence, Florence, Italy-
crisitem.author.deptDipartimento di Chimica, University of Florence, Florence, Italy-
crisitem.author.orcid0000-0002-1351-9683-
crisitem.author.orcid0000-0001-9380-6967-
crisitem.author.orcid0000-0001-7932-2499-
crisitem.author.orcid0000-0001-8872-8917-
crisitem.author.orcid0000-0002-2405-2898-
crisitem.author.orcid0000-0001-6326-2612-
crisitem.author.orcid0000-0002-3208-6756-
crisitem.author.parentorgIstituto Nazionale di Geofisica e Vulcanologia-
crisitem.classification.parent01. Atmosphere-
crisitem.department.parentorgIstituto Nazionale di Geofisica e Vulcanologia-
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