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In this work we present the isotopic, chemical and dust stratigraphies of two snow pits sampled in 2013/14 at GV7 (coastal East Antarctica: 70°41′ S - 158°51′ E, 1950 m a.s.l.). A large number of chemical species are measured aiming to study their potentiality as environmental changes markers. Seasonal cluster backward trajectories analysis was performed and compared with chemical marker stratigraphies. Sea spray aerosol is delivered to the sampling site together with snow precipitation especially in autumn-winter by air masses arising from Western Pacific Ocean sector. Dust show maximum concentration in spring when the air masses arising from Ross Sea sector mobilize mineral dust from ice-free areas of the Transantarctic mountains. The clear seasonal pattern of sulfur oxidized compounds allows the dating of the snow-pit and the calculation of the mean accumulation rate, which is 242 ± 71 mm w.e. for the period 2008–2013. Methanesulfonic acid and NO3− do not show any concentration decreasing trend as depth increases, also considering a 12 m firn core record. Therefore these two compounds are not affected by post-depositional processes at this site and can be considered reliable markers for past environmental changes reconstruction. The rBC snow-pit record shows the highest values in summer 2012 likely related to large biomass burning even occurred in Australia in this summer. The undisturbed accumulation rate for this site is demonstrated by the agreement between the chemical stratigraphies and the annual accumulation rate of the two snow-pits analysed in Italian and Korean laboratories.

We present results from a systematic study of vertical profiles of aerosol number size distribution and black carbon (BC) concentrations conducted in the Arctic, over Ny-Ålesund (Svalbard). The campaign lasted 2 years (2011-2012) and resulted in 200 vertical profiles measured by means of a tethered balloon (up to 1200 m a.g.l.) during the spring and summer seasons. In addition, chemical analysis of filter samples, aerosol size distribution and a full set of meteorological parameters were determined at ground. The collected experimental data allowed a classification of the vertical profiles into different typologies, which allowed us to describe the seasonal phenomenology of vertical aerosol properties in the Arctic. During spring, four main types of profiles were found and their behavior was related to the main aerosol and atmospheric dynamics occurring at the measuring site. Background conditions generated homogenous profiles. Transport events caused an increase of aerosol concentration with altitude. High Arctic haze pollution trapped below thermal inversions promoted a decrease of aerosol concentration with altitude. Finally, ground-based plumes of locally formed secondary aerosol determined profiles with decreasing aerosol concentration located at different altitude as a function of size. During the summer season, the impact from shipping caused aerosol and BC pollution plumes to be constrained close to the ground, indicating that increasing shipping emissions in the Arctic could bring anthropogenic aerosol and BC in the Arctic summer, affecting the climate.

During the 2013 Arctic campaign, direct measurements and size-segregated samplings of atmospheric aerosol were carried out from March to September at the Gruvebadet observatory in Ny-Ålesund (78°56′N, 11°56′E; Svalbard Islands). Continuous size distribution measurements (104 size classes) were performed both in the nano- (TSI-SMPS system) and micro-metric (TSI-APS device) range with a resolution of 10 min. Aerosol sampling was carried out on daily basis (PM10 fraction, 00:01–23:59 UTC) and with a 4-day resolution (four-stage cascade impactor). A back-trajectory analysis was performed for specific events to understand transport processes and possible source areas of aerosol reaching Ny-Ålesund. Aerosol samples were analyzed for ion composition (inorganic cations and anions, selected organic anions) by a three-chromatograph system after extraction in ultra-sonic bath. Special attention was spent in identifying and interpreting the seasonal pattern of natural and anthropic chemical markers. Sea spray aerosol was evenly distributed along all the sampling period with maxima related to wind speed. Its size distribution peaks in 1.0–2.5 or 2.5–10 µm, depending on the transport conditions and distance from source areas. Anthropic sulfate dominates the spring aerosol load (Arctic Haze), both in acidic form (H2SO4) and in partially or totally neutralized ammonium salts. Biogenic contributions, marked by methanesulfonic acid, are relatively relevant in late spring–early summer and are distributed in the finest aerosol fraction (<1.0 µm).

We present results from a systematic study of vertical profiles of aerosol number size distribution and black carbon (BC) concentrations conducted in the Arctic, over Ny-Ålesund (Svalbard). The campaign lasted 2 years (2011-2012) and resulted in 200 vertical profiles measured by means of a tethered balloon (up to 1200 m a.g.l.) during the spring and summer seasons. In addition, chemical analysis of filter samples, aerosol size distribution and a full set of meteorological parameters were determined at ground. The collected experimental data allowed a classification of the vertical profiles into different typologies, which allowed us to describe the seasonal phenomenology of vertical aerosol properties in the Arctic. During spring, four main types of profiles were found and their behavior was related to the main aerosol and atmospheric dynamics occurring at the measuring site. Background conditions generated homogenous profiles. Transport events caused an increase of aerosol concentration with altitude. High Arctic haze pollution trapped below thermal inversions promoted a decrease of aerosol concentration with altitude. Finally, ground-based plumes of locally formed secondary aerosol determined profiles with decreasing aerosol concentration located at different altitude as a function of size. During the summer season, the impact from shipping caused aerosol and BC pollution plumes to be constrained close to the ground, indicating that increasing shipping emissions in the Arctic could bring anthropogenic aerosol and BC in the Arctic summer, affecting the climate.

Aerosol samplings were performed both at ground level and at different heights upon the Ny-Ålesund polar station in June–July 2012 using a tethered balloon equipped with a sampling pump and meteorological sensors. The samples were analyzed by ion chromatography and scanning electron microscopy to characterize the sources and the evolution of the aerosol particles in the planetary boundary layer. The results show the main contribution of long-range over local/regional transported particles and sediments in the aerosols in the period of interest. Among the long-range sources, a main contribution was represented by Siberian local soils and regional wildfires which provided typical particles (metal oxides, calcareous grains), and ion species (nss-K+, nss-SO42−) to the aerosols. Among the local sources, a main contribution was represented by fly ash emitted by the cruise ships frequently landing around Ny-Ålesund during summer. Another aspect which results from aerosol particle characterization is the clear stratification of the planetary boundary layer upon Ny-Ålesund. This typical feature, which has been already documented in spring on the same site (Moroni et al. 2015), is quite effective also in summertime despite the higher potential of local dust production and the lower atmospheric stability characterizing this period.

In this work, an evaluation of an intense biomass burning event observed over Ny-angstrom lesund (Spitsbergen, European Arctic) in July 2015 is presented. Data from the multi-wavelengths Raman-lidar KARL, a sun photometer and radiosonde measurements are used to derive some microphysical properties of the biomass burning aerosol as size distribution, refractive index and single scattering albedo at different relative humidities. Predominantly particles in the accumulation mode have been found with a bi-modal distribution and dominance of the smaller mode. Above 80% relative humidity, hygroscopic growth in terms of an increase of particle diameter and a slight decrease of the index of refraction (real and imaginary part) has been found. Values of the single scattering albedo around 0.9 both at 355nm and 532nm indicate some absorption by the aerosol. Values of the lidar ratio are around 26sr for 355nm and around 50sr for 532nm, almost independent of the relative humidity. Further, data from the photometer and surface radiation values from the local baseline surface radiation network (BSRN) have been applied to derive the radiative impact of the biomass burning event purely from observational data by comparison with a clear background day. We found a strong cooling for the visible radiation and a slight warming in the infra-red. The net aerosol forcing, derived by comparison with a clear background day purely from observational data, obtained a value of -95 W/m(2) per unit AOD500.

BACKGROUND: Platinum-based drugs such as Cisplatin are commonly employed for cancer treatment. Despite an initial therapeutic response, Cisplatin treatment often results in the development of chemoresistance. To identify novel approaches to overcome Cisplatin resistance, we tested Cisplatin in combination with K+ channel modulators on colorectal cancer (CRC) cells. METHODS: The functional expression of Ca2+-activated (KCa3.1, also known as KCNN4) and voltage-dependent (Kv11.1, also known as KCNH2 or hERG1) K+ channels was determined in two CRC cell lines (HCT-116 and HCT-8) by molecular and electrophysiological techniques. Cisplatin and several K+ channel modulators were tested in vitro for their action on K+ currents, cell vitality, apoptosis, cell cycle, proliferation, intracellular signalling and Platinum uptake. These effects were also analysed in a mouse model mimicking Cisplatin resistance. RESULTS: Cisplatin-resistant CRC cells expressed higher levels of KCa3.1 and Kv11.1 channels, compared with Cisplatin-sensitive CRC cells. In resistant cells, KCa3.1 activators (SKA-31) and Kv11.1 inhibitors (E4031) had a synergistic action with Cisplatin in triggering apoptosis and inhibiting proliferation. The effect was maximal when KCa3.1 activation and Kv11.1 inhibition were combined. In fact, similar results were produced by Riluzole, which is able to both activate KCa3.1 and inhibit Kv11.1. Cisplatin uptake into resistant cells depended on KCa3.1 channel activity, as it was potentiated by KCa3.1 activators. Kv11.1 blockade led to increased KCa3.1 expression and thereby stimulated Cisplatin uptake. Finally, the combined administration of a KCa3.1 activator and a Kv11.1 inhibitor also overcame Cisplatin resistance in vivo. CONCLUSIONS: As Riluzole, an activator of KCa3.1 and inhibitor of Kv11.1 channels, is in clinical use, our results suggest that this compound may be useful in the clinic to improve Cisplatin efficacy and overcome Cisplatin resistance in CRC

In this work, an evaluation of an intense biomass burning event observed over Ny-Ålesund (Spitsbergen, European Arctic) in July 2015 is presented. Data from the multi-wavelengths Raman-lidar KARL, a sun photometer and radiosonde measurements are used to derive some microphysical properties of the biomass burning aerosol as size distribution, refractive index and single scattering albedo at different relative humidities. Predominantly particles in the accumulation mode have been found with a bi-modal distribution and dominance of the smaller mode. Above 80% relative humidity, hygroscopic growth in terms of an increase of particle diameter and a slight decrease of the index of refraction (real and imaginary part) has been found. Values of the single scattering albedo around 0.9 both at 355 nm and 532 nm indicate some absorption by the aerosol. Values of the lidar ratio are around 26 sr for 355 nm and around 50 sr for 532 nm, almost independent of the relative humidity. Further, data from the photometer and surface radiation values from the local baseline surface radiation network (BSRN) have been applied to derive the radiative impact of the biomass burning event purely from observational data by comparison with a clear background day. We found a strong cooling for the visible radiation and a slight warming in the infra-red. The net aerosol forcing, derived by comparison with a clear background day purely from observational data, obtained a value of –95 W/m2 per unit AOD500.

BACKGROUND: Platinum-based drugs such as Cisplatin are commonly employed for cancer treatment. Despite an initial therapeutic response, Cisplatin treatment often results in the development of chemoresistance. To identify novel approaches to overcome Cisplatin resistance, we tested Cisplatin in combination with K+ channel modulators on colorectal cancer (CRC) cells. METHODS: The functional expression of Ca2+-activated (KCa3.1, also known as KCNN4) and voltage-dependent (Kv11.1, also known as KCNH2 or hERG1) K+ channels was determined in two CRC cell lines (HCT-116 and HCT-8) by molecular and electrophysiological techniques. Cisplatin and several K+ channel modulators were tested in vitro for their action on K+ currents, cell vitality, apoptosis, cell cycle, proliferation, intracellular signalling and Platinum uptake. These effects were also analysed in a mouse model mimicking Cisplatin resistance. RESULTS: Cisplatin-resistant CRC cells expressed higher levels of KCa3.1 and Kv11.1 channels, compared with Cisplatin-sensitive CRC cells. In resistant cells, KCa3.1 activators (SKA-31) and Kv11.1 inhibitors (E4031) had a synergistic action with Cisplatin in triggering apoptosis and inhibiting proliferation. The effect was maximal when KCa3.1 activation and Kv11.1 inhibition were combined. In fact, similar results were produced by Riluzole, which is able to both activate KCa3.1 and inhibit Kv11.1. Cisplatin uptake into resistant cells depended on KCa3.1 channel activity, as it was potentiated by KCa3.1 activators. Kv11.1 blockade led to increased KCa3.1 expression and thereby stimulated Cisplatin uptake. Finally, the combined administration of a KCa3.1 activator and a Kv11.1 inhibitor also overcame Cisplatin resistance in vivo. CONCLUSIONS: As Riluzole, an activator of KCa3.1 and inhibitor of Kv11.1 channels, is in clinical use, our results suggest that this compound may be useful in the clinic to improve Cisplatin efficacy and overcome Cisplatin resistance in CRC

Atmospheric new particle formation and growth significantly influences climate by supplying new seeds for cloud condensation and brightness. Currently, there is a lack of understanding of whether and how marine biota emissions affect aerosol-cloud-climate interactions in the Arctic. Here, the aerosol population was categorised via cluster analysis of aerosol size distributions taken at Mt Zeppelin (Svalbard) during a 11 year record (2000-2010) and at Station Nord (Greenland) during a 7 year period (2010-2016). Air mass trajectory analysis and atmospheric nitrogen and sulphur tracers link these frequent nucleation events to biogenic precursors released by open water and melting sea ice regions. The occurrence of such events across both temporal periods (2000-2010 and 2010-2016) are anti-correlated with sea ice extent

Size-segregated particle samples were collected in the Arctic (Ny-Ålesund, Svalbard) in April 2011 both at ground level and in the free atmosphere exploiting a tethered balloon equipped also with an optical particle counter (OPC) and meteorological sensors. Individual particle properties were investigated by scanning electron microscopy coupled with energy dispersive microanalysis (SEM-EDS). Results of the SEM-EDS were integrated with particle size and optical measurements of the aerosols properties at ground level and along the vertical profiles. Detailed analysis of two case studies reveals significant differences in composition despite the similar structure (layering) and the comparable texture (grain size distribution) of particles in the air column. Differences in the mineral chemistry of samples point at both local (plutonic/metamorphic complexes in Svalbard) and remote (basic/ultrabasic magmatic complexes in Greenland and/or Iceland) geological source regions for dust. Differences in the particle size and shape are put into relationship with the mechanism of particle formation, that is, primary (well sorted, small) or secondary (idiomorphic, fine to coarse grained) origin for chloride and sulfate crystals and transport/settling for soil (silicate, carbonate and metal oxide) particles. The influence of size, shape, and mixing state of particles on ice nucleation and radiative properties is also discussed.

Atmospheric new particle formation (NPF) and growth significantly influences climate by supplying new seeds for cloud condensation and brightness. Currently, there is a lack of understanding of whether and how marine biota emissions affect aerosol-cloud-climate interactions in the Arctic. Here, the aerosol population was categorised via cluster analysis of aerosol size distributions taken at Mt Zeppelin (Svalbard) during a 11 year record. The daily temporal occurrence of NPF events likely caused by nucleation in the polar marine boundary layer was quantified annually as 18%, with a peak of 51% during summer months. Air mass trajectory analysis and atmospheric nitrogen and sulphur tracers link these frequent nucleation events to biogenic precursors released by open water and melting sea ice regions. The occurrence of such events across a full decade was anti-correlated with sea ice extent. New particles originating from open water and open pack ice increased the cloud condensation nuclei concentration background by at least ca. 20%, supporting a marine biosphere-climate link through sea ice melt and low altitude clouds that may have contributed to accelerate Arctic warming. Our results prompt a better representation of biogenic aerosol sources in Arctic climate models.

Antarctic sea ice has shown an increasing trend in recent decades, but with strong regional differences from one sector to another of the Southern Ocean. The Ross Sea and the Indian sectors have seen an increase in sea ice during the satellite era (1979 onwards). Here we present a record of ssNa+ flux in the Talos Dome region during a 25-year period spanning from 1979 to 2003, showing that this marker could be used as a potential proxy for reconstructing the sea ice extent in the Ross Sea and Western Pacific Ocean at least for recent decades. After finding a positive relationship between the maxima in sea ice extent for a 25-year period, we used this relationship in the TALDICE record in order to reconstruct the sea ice conditions over the 20th century. Our tentative reconstruction highlighted a decline in the sea ice extent (SIE) starting in the 1950s and pointed out a higher variability of SIE starting from the 1960s and that the largest sea ice extents of the last century occurred during the 1990s.

Antarctic sea ice has shown an increasing trend in recent decades, but with strong regional differences from one sector to another of the Southern Ocean. The Ross Sea and the Indian sectors have seen an increase in sea ice during the satellite era (1979 onwards). Here we present a record of ssNa+ flux in the Talos Dome region during a 25-year period spanning from 1979 to 2003, showing that this marker could be used as a potential proxy for reconstructing the sea ice extent in the Ross Sea and Western Pacific Ocean at least for recent decades. After finding a positive relationship between the maxima in sea ice extent for a 25-year period, we used this relationship in the TALDICE record in order to reconstruct the sea ice conditions over the 20th century. Our tentative reconstruction highlighted a decline in the sea ice extent (SIE) starting in the 1950s and pointed out a higher variability of SIE starting from the 1960s and that the largest sea ice extents of the last century occurred during the 1990s.

Ice-core records of climate from Greenland and Antarctica show asynchronous temperature variations on millennial timescales during the last glacial period. The warming during the transition from glacial to interglacial conditions was markedly different between the hemispheres, a pattern attributed to the thermal bipolar see-saw. However, a record from the Ross Sea sector of East Antarctica has been suggested to be synchronous with Northern Hemisphere climate change. Here we present a temperature record from the Talos Dome ice core, also located in the Ross Sea sector. We compare our record with ice-core analyses from Greenland, based on methane synchronization, and find clearly asynchronous temperature changes during the deglaciation. We also find distinct differences in Antarctic records, pointing to differences in the climate evolution of the Indo-Pacific and Atlantic sectors of Antarctica. In the Atlantic sector, we find that the rate of warming slowed between 16,000 and 14,500 years ago, parallel with the deceleration of the rise in atmospheric carbon dioxide concentrations and with a slight cooling over Greenland. In addition, our chronology supports the hypothesis that the cooling of the Antarctic Cold Reversal is synchronous with the Bølling-Allerød warming in the northern hemisphere 14,700 years ago. © 2011 Macmillan Publishers Limited. All rights reserved.

In this paper impact of intensive biomass burning (BB) in North America in July 2015, on aerosol optical and microphysical properties measured in the European Arctic is discussed. This study was made within the framework of the Impact of Absorbing Aerosols on radiating forcing in the European Arctic (iAREA) project. During the BB event aerosol optical depth (AOD) at 500 nm exceeded 1.2 in Spitsbergen and 0.7 in Andenes (Norway). Ångström Exponent (AE) exceeded 1.4 while the absorbing Ångström Exponent (AAE) varied between 1 and 1.25. BB aerosols were observed in humid atmosphere with a total water vapor column between 2 and 2.5 cm. In such conditions aerosols are activated and may produce clouds at different altitudes. Vertical structure of aerosol plumes over Svalbard, obtained from ceilometers and lidars, shows variability of range corrected signal between surface and middle and upper troposphere. Aerosol backscattering coefficients show values up to 10 -5m-1sr-1at 532 nm. Aerosol surface observations indicate chemical composition typical for biomass burning particles and very high single scattering properties. Scattering and absorption coefficients at 530 nm were up to 130 and 15 Mm-1, respectively. Single scattering albedo at the surface varied from 0.9 to 0.94. The averaged values over the entire atmospheric column, ranged from 0.93 to 0.99. Preliminary statistics of model and sunphotometer data as well as previous studies indicate that this event, in the Arctic region, must be considered extreme (such AOD was not observed in Svalbard since 2005) with a significant impact on energy budget.

In this work multi wavelength Raman lidar data from Ny-Ålesund, Spitsbergen have been analysed for the spring 2014 Arctic haze season, as part of the iAREA campaign. Typical values and probability distributions for aerosol backscatter, extinction and depolarisation, the lidar ratio and the color ratio for 4 different altitude intervals within the troposphere are given. These quantities and their dependencies are analysed and the frequency of altitude-dependent observed aerosol events are given. A comparison with ground-based size distribution and chemical composition is performed. Hence the aim of this paper is to provide typical and statistically meaningful properties of Arctic aerosol, which may be used in climate models or to constrain the radiative forcing. We have found that the 2014 season was only moderately polluted with Arctic haze and that sea salt and sulphate were the most dominant aerosol species. Moreover the drying of an aerosol layer after cloud disintegration has been observed. Hardly any clear temporal evolution over the 4 week data set on Arctic haze is obvious with the exception of the extinction coefficient and the lidar ratio, which significantly decreased below 2 km altitude by end April. In altitudes between 2 and 5 km the haze season lasted longer and the aerosol properties were generally more homogeneous than closer to the surface. Above 5 km only few particles were found. The variability of the lidar ratio is discussed. It was found that knowledge of the aerosol’s size and shape does not determine the lidar ratio. Contrary to shape and lidar ratio, there is a clear correlation between size and backscatter: larger particles show a higher backscatter coefficient.

In this paper impact of intensive biomass burning (BB) in North America in July 2015, on aerosol optical and microphysical properties measured in the European Arctic is discussed. This study was made within the framework of the Impact of Absorbing Aerosols on radiating forcing in the European Arctic (iAREA) project. During the BB event aerosol optical depth (AOD) at 500 nm exceeded 1.2 in Spitsbergen and 0.7 in Andenes (Norway). Ångström Exponent (AE) exceeded 1.4 while the absorbing Ångström Exponent (AAE) varied between 1 and 1.25. BB aerosols were observed in humid atmosphere with a total water vapor column between 2 and 2.5 cm. In such conditions aerosols are activated and may produce clouds at different altitudes. Vertical structure of aerosol plumes over Svalbard, obtained from ceilometers and lidars, shows variability of range corrected signal between surface and middle and upper troposphere. Aerosol backscattering coefficients show values up to 10 -5m-1sr-1at 532 nm. Aerosol surface observations indicate chemical composition typical for biomass burning particles and very high single scattering properties. Scattering and absorption coefficients at 530 nm were up to 130 and 15 Mm-1, respectively. Single scattering albedo at the surface varied from 0.9 to 0.94. The averaged values over the entire atmospheric column, ranged from 0.93 to 0.99. Preliminary statistics of model and sunphotometer data as well as previous studies indicate that this event, in the Arctic region, must be considered extreme (such AOD was not observed in Svalbard since 2005) with a significant impact on energy budget.

In this work multi wavelength Raman lidar data from Ny-Ålesund, Spitsbergen have been analysed for the spring 2014 Arctic haze season, as part of the iAREA campaign. Typical values and probability distributions for aerosol backscatter, extinction and depolarisation, the lidar ratio and the color ratio for 4 different altitude intervals within the troposphere are given. These quantities and their dependencies are analysed and the frequency of altitude-dependent observed aerosol events are given. A comparison with ground-based size distribution and chemical composition is performed. Hence the aim of this paper is to provide typical and statistically meaningful properties of Arctic aerosol, which may be used in climate models or to constrain the radiative forcing. We have found that the 2014 season was only moderately polluted with Arctic haze and that sea salt and sulphate were the most dominant aerosol species. Moreover the drying of an aerosol layer after cloud disintegration has been observed. Hardly any clear temporal evolution over the 4 week data set on Arctic haze is obvious with the exception of the extinction coefficient and the lidar ratio, which significantly decreased below 2 km altitude by end April. In altitudes between 2 and 5 km the haze season lasted longer and the aerosol properties were generally more homogeneous than closer to the surface. Above 5 km only few particles were found. The variability of the lidar ratio is discussed. It was found that knowledge of the aerosol’s size and shape does not determine the lidar ratio. Contrary to shape and lidar ratio, there is a clear correlation between size and backscatter: larger particles show a higher backscatter coefficient.

Daily PM10 aerosol samples were collected at the Gruvebadet observatory, Ny-Ålesund (Svalbard Islands), during the spring-summer 2014 Italian Arctic Campaign. A total of 136 samples were analysed for ion (inorganic anions and cations, selected organic anions) composition aiming to evaluate the seasonal pattern of sulfate, as a key component of the Arctic haze. Ionic balances indicated a strong sulfate seasonality with mean spring concentration about 1.5 times higher than that measured in summer. The spring and summer aerosol was almost neutral, indicating that ammonia was the major neutralizing agent for atmospheric acidic species. The linear regression between sulfate from potential acidic sources (non-sea salt sulfate and non-crustal sulfate) and ammonium indicated that the mean sulfate/ammonium ratio was intermediate between semi-(NH4HSO4) and complete ((NH4)2SO4) neutralization. Using sea-salt sodium as sea-spray marker, non-sea-salt calcium as crustal marker and methanesulfonic acid as biogenic marker, a detailed source apportionment for sulfate was carried out. The anthropogenic input (calculated as the differences between total sulfate and the sum of sea-salt, crustal and biogenic contributes) was found to be the most relevant contribution to the sulfate budget in the Ny-Ålesund aerosol in summer and, especially, in spring. In this last season, crustal, sea-salt, biogenic and anthropogenic sources accounted for 3.3, 12.0, 11.5 and 74.8 %, respectively.

A Flow Injection Analysis (FIA) spectrofluorimetric method for calcium determination in ice cores was optimised in order to achieve better analytical performances which would make it suitable for reliable calcium measurements at ppt level. The method here optimised is based on the formation of a fluorescent compound between Ca and Quin-2 in buffered environment. A careful evaluation of operative parameters (reagent concentration, buffer composition and concentration, pH), influence of interfering species possibly present in real samples and potential favourable effect of surfactant addition was carried out. The obtained detection limit is around 15 ppt, which is one order of magnitude lower than the most sensitive Flow Analysis method for Ca determination currently available in literature and reproducibility is better than 4% for Ca concentrations of 0.2 ppb. The method was validated through measurements performed in parallel with Ion Chromatography on 200 samples from an alpine ice core (Lys Glacier) revealing an excellent fit between the two chemical series. Calcium stratigraphy in Lys ice core was discussed in terms of seasonal pattern and occurrence of Saharan dust events. © 2007 Elsevier B.V. All rights reserved.

Two Holocene ice core records from East Antarctica (Vostok and EPICA-Dome C) were analysed for dust concentration and size distribution at a temporal resolution of 1 sample per similar to 50 years. A series of volcanic markers randomly distributed over the common part of the ice cores (from 9.8 to 3.5 kyear BP) ensures accurate relative dating (+/-33 years). Dust-size records from the two sites display oscillations structured in cycles with sub-millennial and secular scale frequencies that are apparently asynchronous. The power spectra of the composite sum (1) of the two dust-size records display spectral energy mostly for 150- to 500-year periodicities. On the other hand, the 200-year band is common to both records and the 200 year components of the two sites are out-of-phase (100-year lead or lag) over similar to 5.5 kyear, a phenomenon also reflected by a significant ( > 99 % conf. lev.) band in the power spectra of the composite difference (A) of the two size records. During long-range transport, mineral dust originating from the Southern Hemisphere continents is graded to a variable extent depending on the altitude and duration of atmospheric transport. Relatively coarse dust is associated with air mass penetration from the middle-lower troposphere and conversely relatively fine dust with upper troposphere air masses or the influence of subsidence over the Antarctic plateau, a hypothesis already proposed for the changes that occurred during the Last Glacial Maximum to Holocene transition (Delmonte et al. 2004b). Moreover, we assume that the overall fluctuation of air mass advection over Antarctica depends on the meridional pressure gradient with respect to low latitudes, i.e. the Antarctic Oscillation (AAO). We therefore suggest a regional variability in atmospheric circulation over East Antarctica. The 150500 year power spectrum of the composite (1) parameter represents the long term variability of the AAO, imprinted by secular internal oscillations probably r

An important share of paleoclimatic information is buried within the lowermost layers of deep ice cores. Because improving our records further back in time is one of the main challenges in the near future, it is essential to judge how deep these records remain unaltered, since the proximity of the bedrock is likely to interfere both with the recorded temporal sequence and the ice properties. In this paper, we present a multiparametric study (δD-δ18Oice, δ18Oatm, total air content, CO2, CH4, N2O, dust, high resolution chemistry, ice texture) of the bottom 60m of the EPICA Dome C ice core from central Antarctica. These bottom layers have been subdivided in two sections: the lower 12m showing visible solid inclusions (basal ice) and the 48m above which we refer to as “deep ice”. Some of the data are consistent with a pristine paleoclimatic signal, others show clear anomalies. It is demonstrated that neither large scale bottom refreezing of subglacial water, nor mixing (be it internal or with a local basal end-term from a previous/ initial ice sheet configuration) can explain the observed bottom ice properties. We focus on the high-resolution chemical profiles and on the available remote sensing data on the subglacial topography of the site to propose a mechanism by which relative stretching of the bottom ice sheet layers is made possible, due to the progressively confining effect of subglacial valley sides. This stress field change, combined with bottom ice temperature close to the pressure melting point, induces accelerated migration recrystallization, which results in spatial chemical sorting of the impurities, depending on their state (dissolved vs. solid) and if they are involved or not in salt formation. This chemical sorting effect is responsible for the progressive build-up of the visible solid aggregates that therefore mainly originate “from within”, and not from incorporation processes of allochtone material at the ice–bedrock interface. We also discuss how th

An important share of paleoclimatic information is buried within the lowermost layers of deep ice cores. Because improving our records further back in time is one of the main challenges in the near future, it is essential to judge how deep these records remain unaltered, since the proximity of the bedrock is likely to interfere both with the recorded temporal sequence and the ice properties. In this paper, we present a multiparametric study (delta D-delta O-18(ice), delta O-18(atm), total air content, CO2, CH4, N2O, dust, high-resolution chemistry, ice texture) of the bottom 60 m of the EPICA (European Project for Ice Coring in Antarctica) Dome C ice core from central Antarctica. These bottom layers were subdivided into two distinct facies: the lower 12 m showing visible solid inclusions (basal dispersed ice facies) and the upper 48 m, which we will refer to as the basal clean ice facies. Some of the data are consistent with a pristine paleoclimatic signal, others show clear anomalies It is demonstrated that neither large-scale bottom refreezing of subglacial water, nor mixing (be it internal or with a local basal end term from a previous/initial ice sheet configuration) can explain the observed bottom-ice properties. We focus on the high-resolution chemical profiles and on the available remote sensing data on the subglacial topography of the site to propose a mechanism by which relative stretching of the bottom-ice sheet layers is made possible, due to the progressively confining effect of subglacial valley sides. This stress field change, combined with bottom-ice temperature close to the pressure melting point, induces accelerated migration recrystallization, which results in spatial chemical sorting of the impurities, depending on their state (dissolved vs. solid) and if they are involved or not in salt formation. This chemical sorting effect is responsible for the progressive build-up of the visible solid aggregates that therefore mainly originate from within, a

Size-segregated particle samples were collected in the Arctic (Ny-Ålesund, Svalbard) in April 2011 both at ground level and in the free atmosphere exploiting a tethered balloon equipped also with an optical particle counter (OPC) and meteorological sensors. Individual particle properties were investigated by scanning electron microscopy coupled with energy dispersive microanalysis (SEM-EDS). Results of the SEM-EDS were integrated with particle size and optical measurements of the aerosols properties at ground level and along the vertical profiles. Detailed analysis of two case studies reveals significant differences in composition despite the similar structure (layering) and the comparable texture (grain size distribution) of particles in the air column. Differences in the mineral chemistry of samples point at both local (plutonic/metamorphic complexes in Svalbard) and remote (basic/ultrabasic magmatic complexes in Greenland and/or Iceland) geological source regions for dust. Differences in the particle size and shape are put into relationship with the mechanism of particle formation, that is, primary (well sorted, small) or secondary (idiomorphic, fine to coarse grained) origin for chloride and sulfate crystals and transport/settling for soil (silicate, carbonate and metal oxide) particles. The influence of size, shape, and mixing state of particles on ice nucleation and radiative properties is also discussed.

Size-segregated particle samples were collected in the Arctic (Ny-Ålesund, Svalbard) in April 2011 both at ground level and in the free atmosphere exploiting a tethered balloon equipped also with an optical particle counter (OPC) and meteorological sensors. Individual particle properties were investigated by scanning electron microscopy coupled with energy dispersive microanalysis (SEM-EDS). Results of the SEM-EDS were integrated with particle size and optical measurements of the aerosols properties at ground level and along the vertical profiles. Detailed analysis of two case studies reveals significant differences in composition despite the similar structure (layering) and the comparable texture (grain size distribution) of particles in the air column. Differences in the mineral chemistry of samples point at both local (plutonic/metamorphic complexes in Svalbard) and remote (basic/ultrabasic magmatic complexes in Greenland and/or Iceland) geological source regions for dust. Differences in the particle size and shape are put into relationship with the mechanism of particle formation, that is, primary (well sorted, small) or secondary (idiomorphic, fine to coarse grained) origin for chloride and sulfate crystals and transport/settling for soil (silicate, carbonate and metal oxide) particles. The influence of size, shape, and mixing state of particles on ice nucleation and radiative properties is also discussed.

© 2014 R. Traversi et al. Here we present the first multi-year record of nitrate in the atmospheric aerosol (2005-2008) and surface snow (2006-08) from central Antarctica. PM10 and size-segregated aerosol, together with superficial snow, have been collected all year-round at high resolution (daily for all the snow samples and for most of aerosol samples) at Dome C since the 2004/05 field season and analysed for main and trace ionic markers. The suitability of the sampling location in terms of possible contamination from the base is shown in detail. In spite of the relevance of nitrate in Antarctic atmosphere, both for better understanding the chemistry of N cycle in the plateau boundary layer and for improving the interpretation of long-term nitrate records from deep ice core records, nitrate sources in Antarctica are not well constrained yet, neither in extent nor in timing. A recurring seasonal pattern was pointed out in both aerosol and snow records, showing summer maxima and winter minima, although aerosol maxima lead the snow ones of 1-2 months, possibly due to a higher acidity in the atmosphere in mid-summer, favouring the repartition of nitrate as nitric acid and thus its uptake by the surface snow layers. On the basis of a meteorological analysis of one major nitrate event, of data related to PSC I extent and of irradiance values, we propose that the high nitrate summer levels in aerosol and snow are likely due to a synergy of enhanced source of nitrate and/or its precursors (such as the stratospheric inputs), higher solar irradiance and higher oxidation rates in this season. Moreover, we show here a further evidence of the substantial contribution of HNO3/NOx re-emission from the snowpack, already shown in previous works, and which can explain a significant fraction of atmospheric nitrate, maintaining the same seasonal pattern in the snow. As concerning snow specifically, the presented data suggest that nitrate is likely to be controlled mainly b

The Toba eruption that occurred some 74 ka ago in Sumatra, Indonesia, is among the largest volcanic events on Earth over the last 2 million years. Tephra from this eruption has been spread over vast areas in Asia, where it constitutes a major time marker close to the Marine Isotope Stage 4/5 boundary. As yet, no tephra associated with Toba has been identified in Greenland or Antarctic ice cores. Based on new accurate dating of Toba tephra and on accurately dated European stalagmites, the Toba event is known to occur between the onsets of Greenland interstadials (GI) 19 and 20. Furthermore, the existing linking of Greenland and Antarctic ice cores by gas records and by the bipolar seesaw hypothesis suggests that the Antarctic counterpart is situated between Antarctic Isotope Maxima (AIM) 19 and 20. In this work we suggest a direct synchronization of Greenland (NGRIP) and Antarctic (EDML) ice cores at the Toba eruption based on matching of a pattern of bipolar volcanic spikes. Annual layer counting between volcanic spikes in both cores allows for a unique match. We first demonstrate this bipolar matching technique at the already synchronized Laschamp geomagnetic excursion (41 ka BP) before we apply it to the suggested Toba interval. The Toba synchronization pattern covers some 2000 yr in GI-20 and AIM-19/20 and includes nine acidity peaks that are recognized in both ice cores. The suggested bipolar Toba synchronization has decadal precision. It thus allows a determination of the exact phasing of inter-hemispheric climate in a time interval of poorly constrained ice core records, and it allows for a discussion of the climatic impact of the Toba eruption in a global perspective. The bipolar linking gives no support for a long-term global cooling caused by the Toba eruption as Antarctica experiences a major warming shortly after the event. Furthermore, our bipolar match provides a way to place palaeo-environmental records other than ice cores into a precise climatic cont

The Toba eruption that occurred some 74 ka ago in Sumatra, Indonesia, is among the largest volcanic events on Earth over the last 2 million years. Tephra from this eruption has been spread over vast areas in Asia, where it constitutes a major time marker close to the Marine Isotope Stage 4/5 boundary. As yet, no tephra associated with Toba has been identified in Greenland or Antarctic ice cores. Based on new accurate dating of Toba tephra and on accurately dated European stalagmites, the Toba event is known to occur between the onsets of Greenland interstadials (GI) 19 and 20. Furthermore, the existing linking of Greenland and Antarctic ice cores by gas records and by the bipolar seesaw hypothesis suggests that the Antarctic counterpart is situated between Antarctic Isotope Maxima (AIM) 19 and 20. In this work we suggest a direct synchronization of Greenland (NGRIP) and Antarctic (EDML) ice cores at the Toba eruption based on matching of a pattern of bipolar volcanic spikes. Annual layer counting between volcanic spikes in both cores allows for a unique match. We first demonstrate this bipolar matching technique at the already synchronized Laschamp geomagnetic excursion (41 ka BP) before we apply it to the suggested Toba interval. The Toba synchronization pattern covers some 2000 yr in GI-20 and AIM-19/20 and includes nine acidity peaks that are recognized in both ice cores. The suggested bipolar Toba synchronization has decadal precision. It thus allows a determination of the exact phasing of inter-hemispheric climate in a time interval of poorly constrained ice core records, and it allows for a discussion of the climatic impact of the Toba eruption in a global perspective. The bipolar linking gives no support for a long-term global cooling caused by the Toba eruption as Antarctica experiences a major warming shortly after the event. Furthermore, our bipolar match provides a way to place palaeo-environmental records other than ice cores into a precise climatic cont

The proceedings contain 36 papers. The topics discussed include: real time monitoring of urban particulate matter on a mobile platform; aspects about air pollution prediction on urban environment; water pollution detection; Raman probe of pollutants in water: measurement process; sensor network for environment monitoring: water quality case study; the use of a multiwavelength lidar to detect aerosol layers in the atmosphere; an artificial neural network approach to investigate cavitating flow regime at different temperatures; spectral characterization of solar cells for indoor wireless sensor nodes; microscale dielectric barrier discharge plasma actuators: experimental characterization; evaluation of the relation between building materials and indoor radon pollution; and a smart robotic arm for automatic sorting of objects with different tags.

This study aims at refining the synchronisation between the EPICA Dome C (EDC) and Vostok ice cores in the time interval 0–145 kyr BP by using the volcanic signatures. 102 common volcanic events were identified by using continuous electrical conductivity (ECM), di-electrical profiling (DEP) and sulfate measurements while trying to minimize the distortion of the glaciological chronologies. This is an update and a continuation of previous works performed over the 0–45 kyr interval that provided 56 tie points to the ice core chronologies (Udisti et al., 2004). This synchronisation will serve to establish Antarctic Ice Core Chronology 2012, the next synchronised Antarctic dating. A change of slope in the EDC-depth/Vostok-depth diagram is probably related to a change of accumulation regime as well as to a change of ice thickness upstream of the Lake Vostok, but we did not invoke any significant temporal change of surface accumulation at EDC relative to Vostok. No significant phase difference is detected between the EDC and Vostok isotopic records, but depth shifts between the Vostok 3G and 5G ice cores prevent from looking at this problem accurately. Three possible candidates for the Toba volcanic super-eruption �73 kyr ago are suggested in the Vostok and EDC volcanic records. Neither the ECM, DEP nor the sulfate fingerprints for these 3 events are significantly larger than many others in the records.

Durante 3 anni (2006-2009) sono state svolte campagne di misura estese per la misura della concentrazione e composizione chimica di PM2.5 in 3 siti del Nord Italia: un sito urbano (Milano, MI), un sito rurale (Oasi Le Bine, OB) e un sito remoto di alta quota (Alpe San Colombano, ASC, m. 2280 slm). I campioni di PM2.5 sono stati analizzati per: EC, OC, ioni inorganici, elementi, alcani lineari C20-C32, acidi mono e dicarbossilici C2-C5, levoglucosano LEVO e idrocarburi policiclici aromatici IPA [1]. E’ stato utilizzato in un modello recettore CMB (Chemical Mass Balance; CMB8.2-EPA) per la stima delle sorgenti di PM2.5 nei 3 siti, e nelle diverse stagioni. In particolare, sono stati considerati 13 marker di sorgenti (fitting species: Al, Si, Fe, Pb, EC, LEVO, C29, C31, BbF, BkF, BeP, IcdP, BghiP) per la stima di 5 sorgenti primarie di OC (combustione di biomasse, combustione di gas naturale, contributo primario della vegetazione, risospensione, traffico), da cui è stata ricostruita la stima delle 5 sorgenti primarie e 4 secondarie (ammonio, solfato e nitrato secondario; organico secondario) alle concentrazioni di PM2.5. Un aspetto critico in uno studio di source apportionment mediante modello CMB è la disponibilità di profili di sorgente che siano rappresentativi delle emissioni aggregate per un certo tipo di sorgente e delle reali condizioni per i siti recettori considerati. In questo studio sono stati utilizzati profili di sorgente sperimentali rappresentativi delle reali condizioni del Nord Italia, dove disponibili (traffico, combustione di biomassa e risospensione) [2][3], e profili compositi da dati di letteratura. Sono stati quindi effettuati studi di sensibilità per i risultati del modello CMB, in relazione alla scelta di diversi profili di sorgente selezionati, in particolare traffico e combustione di biomassa. La sorgente traffico è stimata come la sorgente primaria principale (17-24%) alle concentrazioni di PM2.5 in MI, in tutte le stagioni, insieme al contr

The climate of the last glacial Marine Isotopic Stage 3 (MIS3) period is characterized by strong millennial-scale variability with a succession of Dansgaard–Oeschger events first identified in Greenland ice cores and associated with variations of the Atlantic Meridional Overturning Circulation (AMOC). These abrupt events have a smooth and lagged counterpart in water stable isotopes from Antarctic ice cores. In this study we aim at depicting and understanding the circum-Antarctic expression of this millennial-scale variability. To illustrate the mechanisms potentially at work in the response of the southern high latitudes to an abrupt decrease of the AMOC, we first present results from experiments performed with the IPSL-CM4 atmosphere-ocean coupled model under glacial boundary conditions. When the AMOC is perturbed by imposing an additional freshwater flux in the North Atlantic, our model produces the classical bipolar seesaw mechanism generally invoked to explain the warming of the Southern Ocean/Antarctic region. However, this mechanism can be locally offset by faster atmospheric teleconnections originating from the tropics, even though the precise location of this fast response is not coherent among different climate models. Our model results are confronted with a synthesis of Antarctic records of ice core stable isotope and sea-salt sodium, including new data obtained on the TALDICE ice core. The IPSL-CM4 produces a dipole-like pattern around Antarctica, with warming in the Atlantic/Indian sectors contrasting with an unexpected cooling in the East-Pacific sector. The latter signal is not detected in our data synthesis. Both ice core data and simulations are consistent in depicting a more rapid response of the Atlantic sector compared to the Indian sector. This feature can be explained by the gradual impact of ocean transport on which faster atmospheric teleconnections are superimposed. Detailed investigations of the sequence of events between different proxies a

The climate of the last glacial Marine Isotopic Stage 3 (MIS3) period is characterized by strong millennial-scale variability with a succession of Dansgaard–Oeschger events first identified in Greenland ice cores and associated with variations of the Atlantic Meridional Overturning Circulation (AMOC). These abrupt events have a smooth and lagged counterpart in water stable isotopes from Antarctic ice cores. In this study we aim at depicting and understanding the circum-Antarctic expression of this millennial-scale variability. To illustrate the mechanisms potentially at work in the response of the southern high latitudes to an abrupt decrease of the AMOC, we first present results from experiments performed with the IPSL-CM4 atmosphere-ocean coupled model under glacial boundary conditions. When the AMOC is perturbed by imposing an additional freshwater flux in the North Atlantic, our model produces the classical bipolar seesaw mechanism generally invoked to explain the warming of the Southern Ocean/Antarctic region. However, this mechanism can be locally offset by faster atmospheric teleconnections originating from the tropics, even though the precise location of this fast response is not coherent among different climate models. Our model results are confronted with a synthesis of Antarctic records of ice core stable isotope and sea-salt sodium, including new data obtained on the TALDICE ice core. The IPSL-CM4 produces a dipole-like pattern around Antarctica, with warming in the Atlantic/Indian sectors contrasting with an unexpected cooling in the East-Pacific sector. The latter signal is not detected in our data synthesis. Both ice core data and simulations are consistent in depicting a more rapid response of the Atlantic sector compared to the Indian sector. This feature can be explained by the gradual impact of ocean transport on which faster atmospheric teleconnections are superimposed. Detailed investigations of the sequence of events between different proxies a

Durante 3 anni (2006-2009) sono state svolte campagne di misura estese per la misura della concentrazione e composizione chimica di PM2.5 in 3 siti del Nord Italia: un sito urbano (Milano, MI), un sito rurale (Oasi Le Bine, OB) e un sito remoto di alta quota (Alpe San Colombano, ASC, m. 2280 slm). I campioni di PM2.5 sono stati analizzati per: EC, OC, ioni inorganici, elementi, alcani lineari C20-C32, acidi mono e dicarbossilici C2-C5, levoglucosano LEVO e idrocarburi policiclici aromatici IPA [1]. E’ stato utilizzato in un modello recettore CMB (Chemical Mass Balance; CMB8.2-EPA) per la stima delle sorgenti di PM2.5 nei 3 siti, e nelle diverse stagioni. In particolare, sono stati considerati 13 marker di sorgenti (fitting species: Al, Si, Fe, Pb, EC, LEVO, C29, C31, BbF, BkF, BeP, IcdP, BghiP) per la stima di 5 sorgenti primarie di OC (combustione di biomasse, combustione di gas naturale, contributo primario della vegetazione, risospensione, traffico), da cui è stata ricostruita la stima delle 5 sorgenti primarie e 4 secondarie (ammonio, solfato e nitrato secondario; organico secondario) alle concentrazioni di PM2.5. Un aspetto critico in uno studio di source apportionment mediante modello CMB è la disponibilità di profili di sorgente che siano rappresentativi delle emissioni aggregate per un certo tipo di sorgente e delle reali condizioni per i siti recettori considerati. In questo studio sono stati utilizzati profili di sorgente sperimentali rappresentativi delle reali condizioni del Nord Italia, dove disponibili (traffico, combustione di biomassa e risospensione) [2][3], e profili compositi da dati di letteratura. Sono stati quindi effettuati studi di sensibilità per i risultati del modello CMB, in relazione alla scelta di diversi profili di sorgente selezionati, in particolare traffico e combustione di biomassa. La sorgente traffico è stimata come la sorgente primaria principale (17-24%) alle concentrazioni di PM2.5 in MI, in tutte le stagioni, insieme al