References of "Delille, Bruno"      in Complete repository Arts & humanities   Archaeology   Art & art history   Classical & oriental studies   History   Languages & linguistics   Literature   Performing arts   Philosophy & ethics   Religion & theology   Multidisciplinary, general & others Business & economic sciences   Accounting & auditing   Production, distribution & supply chain management   Finance   General management & organizational theory   Human resources management   Management information systems   Marketing   Strategy & innovation   Quantitative methods in economics & management   General economics & history of economic thought   International economics   Macroeconomics & monetary economics   Microeconomics   Economic systems & public economics   Social economics   Special economic topics (health, labor, transportation…)   Multidisciplinary, general & others Engineering, computing & technology   Aerospace & aeronautics engineering   Architecture   Chemical engineering   Civil engineering   Computer science   Electrical & electronics engineering   Energy   Geological, petroleum & mining engineering   Materials science & engineering   Mechanical engineering   Multidisciplinary, general & others Human health sciences   Alternative medicine   Anesthesia & intensive care   Cardiovascular & respiratory systems   Dentistry & oral medicine   Dermatology   Endocrinology, metabolism & nutrition   Forensic medicine   Gastroenterology & hepatology   General & internal medicine   Geriatrics   Hematology   Immunology & infectious disease   Laboratory medicine & medical technology   Neurology   Oncology   Ophthalmology   Orthopedics, rehabilitation & sports medicine   Otolaryngology   Pediatrics   Pharmacy, pharmacology & toxicology   Psychiatry   Public health, health care sciences & services   Radiology, nuclear medicine & imaging   Reproductive medicine (gynecology, andrology, obstetrics)   Rheumatology   Surgery   Urology & nephrology   Multidisciplinary, general & others Law, criminology & political science   Civil law   Criminal law & procedure   Criminology   Economic & commercial law   European & international law   Judicial law   Metalaw, Roman law, history of law & comparative law   Political science, public administration & international relations   Public law   Social law   Tax law   Multidisciplinary, general & others Life sciences   Agriculture & agronomy   Anatomy (cytology, histology, embryology...) & physiology   Animal production & animal husbandry   Aquatic sciences & oceanology   Biochemistry, biophysics & molecular biology   Biotechnology   Entomology & pest control   Environmental sciences & ecology   Food science   Genetics & genetic processes   Microbiology   Phytobiology (plant sciences, forestry, mycology...)   Veterinary medicine & animal health   Zoology   Multidisciplinary, general & others Physical, chemical, mathematical & earth Sciences   Chemistry   Earth sciences & physical geography   Mathematics   Physics   Space science, astronomy & astrophysics   Multidisciplinary, general & others Social & behavioral sciences, psychology   Animal psychology, ethology & psychobiology   Anthropology   Communication & mass media   Education & instruction   Human geography & demography   Library & information sciences   Neurosciences & behavior   Regional & inter-regional studies   Social work & social policy   Sociology & social sciences   Social, industrial & organizational psychology   Theoretical & cognitive psychology   Treatment & clinical psychology   Multidisciplinary, general & others     Showing results 41 to 60 of 274     1 2 3 4 5 6 7 8     Usuing the Arctic Environment Test Basin to study the dynamics of dissolved organic matter in sea iceThomas, D.N.; Zhou, Jiayun ; Kaartokallio, H. et alConference (2014, July)This is a report from the INTERICE 5 project that used the Arctic Environment Test Basin at HSVA from 21 May to 19 June 2012. The overarching aim was to investigate the physical and biological controls of ... [more ▼]This is a report from the INTERICE 5 project that used the Arctic Environment Test Basin at HSVA from 21 May to 19 June 2012. The overarching aim was to investigate the physical and biological controls of dissolved organic matter incorporation into growing sea ice and the effect of melting once the ice had consolidated. Measurements were also made on the CO2 fluxes at the ice surface in relation to the chemical and biological changes taking place in the ice. The Interice 5 team was a multidisciplinary group of glaciologists, chemists and microbiologists from Belgium, Denmark, Finland, Germany and U.K. They were able to build on the experiences of previous INTERICE 2, 3 & 4 projects to maximize the opportunities from the facility. The preliminary results from the experiment will be presented, in the context of what is known about these processes from field campaigns. [less ▲]Detailed reference viewed: 40 (0 ULg) Physical controls on the storage of methane in landfast sea iceZhou, Jiayun ; Tison, J.-L.; Carnat, G. et alin Cryosphere (The) (2014), 8(3), 1019-1029We report on methane (CH4) dynamics in landfast sea ice, brine and under-ice seawater at Barrow in 2009. The CH4 concentrations in under-ice water ranged between 25.9 and 116.4 nmol L-1sw, indicating a ... [more ▼]We report on methane (CH4) dynamics in landfast sea ice, brine and under-ice seawater at Barrow in 2009. The CH4 concentrations in under-ice water ranged between 25.9 and 116.4 nmol L-1sw, indicating a supersaturation of 700 to 3100 % relative to the atmosphere. In comparison, the CH4 concentrations in sea ice, ranged between 3.4 and 17.2 nmol L-1ice, and the deduced CH4 concentrations in brine, between 13.2 and 677.7 nmol L-1brine. We investigated on the processes explaining the difference in CH4 concentrations between sea ice, brine and the under-ice water, and suggest that biological controls on the storage of CH4 in ice was minor in comparison to the physical controls. Two physical processes regulated the storage of CH4 in our landfast ice samples: bubble formation within the ice and sea ice permeability. Gas bubble formation from solubility changes had favoured the accumulation of CH4 in the ice at the beginning of ice growth. CH4 retention in sea ice was then twice as efficient as that of salt; this also explains the overall higher CH4 concentrations in brine than in the under-ice water. As sea ice thickened, gas bubble formation became less efficient, CH4 was then mainly trapped in the dissolved state. The increase of sea ice permeability during ice melt marked the end of CH4 storage. [less ▲]Detailed reference viewed: 49 (4 ULg) Snow cover and short-term synoptic events drive biogeochemical dynamics in winter Weddell Sea pack ice (AWECS cruise - June to August 2013)Tison, J.-L; Delille, Bruno ; Dieckmann, G. et alConference (2014, April)Detailed reference viewed: 10 (0 ULg) Snow cover and short-term synoptic events drive biogeochemical dynamics in winter Weddell Sea pack ice (AWECS cruise - June to August 2013)Tison, J.-L.; Delille, Bruno ; Dieckmann, G. et alConference (2014, March)This paper presents the preliminary results of an integrated multidisciplinary study of pack ice biogeochemistry in the Weddell Sea during the winter 2013 (June-August). The sea ice biogeochemistry group ... [more ▼]This paper presents the preliminary results of an integrated multidisciplinary study of pack ice biogeochemistry in the Weddell Sea during the winter 2013 (June-August). The sea ice biogeochemistry group was one of the components of the AWECS (Antarctic Winter Ecosystem and Climate Study) cruise (Polarstern ANTXXIX-6). A total of 12 stations were carried out by the sea ice biogeochemistry group, which collected a suite of variables in the fields of physics, inorganic chemistry, gas content and composition, microbiology, biogeochemistry, trace metals and the carbonate system in order to give the best possible description of the sea ice cover and its interactions at interfaces. Samples were collected in the atmosphere above (gas fluxes), in the snow cover, in the bulk ice (ice cores), in the brines (sackholes) and in the sea water below (0m, 1m, 30 m). Here we present the results of basic physico-chemical (T°, bulk ice salinity, brine volumes, brine salinity, Rayleigh numbers) and biological (Chla) measurements in order to give an overview of the general status of the Weddell Sea winter pack ice encountered, and discuss how it controls climate relevant biogeochemical processes. Our results from the first set of 9 stations, mainly sampled along the Greenwich meridian and the easternmost part of the Weddell Sea definitively refute the view of a biogeochemically “frozen” sea ice during the Winter. This has already been demonstrated for the Spring and Summer, but we now see that sea ice sustains considerable biological stocks and activities throughout the Winter, despite the reduced amount of available PAR radiation. Accretion of the snow cover appears to play an essential role in driving biogeochemical activity, through warming from insulation, thus favouring brine transport, be it through potential convection, surface brine migration (brine tubes) or flooding. This results in a “widening” of the internal autumn layer (quite frequent in this rafting-dominated sea ice cover) and increase of the chla burden with age. Results from the second set of 3 stations in the western branch of the Weddell Sea gyre confirm that it comprises a mixture of older fast/second year ice floes with younger first-year ice floes. The older ice had the highest Chla concentrations of the entire cruise (>200 mgl-1), in an internal community enclosed within desalinized impermeable upper and lower layers. The first-year ice differs from that in the eastern Weddell Sea as it is dominated by columnar ice and (weak) algal communities are only found on the bottom or near the surface (no internal maximum). [less ▲]Detailed reference viewed: 104 (2 ULg) Investigating iron and organic matter incorporation in growing sea iceJanssens, J.; Delille, Bruno ; de Jong et alConference (2014, March)High concentration of exopolysacharides (EPS) and iron have been found in sea ice surrounding the Antarctic continent. However, the mechanisms leading to that enrichment remain unclear. Scavenging of iron ... [more ▼]High concentration of exopolysacharides (EPS) and iron have been found in sea ice surrounding the Antarctic continent. However, the mechanisms leading to that enrichment remain unclear. Scavenging of iron by organic matter in seawater and entrainment during sea ice formation are thought to be responsible for the accumulation of iron in sea ice. EPS could also play a role in the iron passive chelative scavenging process in sea ice and in the increase of iron bioavailability. Our study investigates the processes responsible for the accumulation of iron (dissolved, particulate and total dissolvable iron), EPS, dissolved and particulate organic matter, macro-nutrients (silicic acid, nitrate and nitrite, phosphoric acid and ammonium), chlorophyll a and sea ice algae in young sea ice during an Australian-lead spring voyage off East Antarctica (SIPEX II September – November 2012) and a German-lead winter voyage to the Weddell Sea (AWECS June – August 2013). We used a combination of field- (“in situ”) and laboratory- based sea ice growth time-series experiments. In addition different types of newly formed sea ice as pancake ice, grey ice, frost flowers and slush were collected during both voyages as a means to compare and validate the experimental data. To our knowledge, this is the first report on the biogeochemical properties of newly formed Antarctic pack ice samples in the winter. Ice temperature, salinity and textures are also presented to support the biogeochemical observations at the onset of sea ice formation. [less ▲]Detailed reference viewed: 137 (1 ULg) Sea ice CO2 flux in the Southern Ocean during mid-winter and early springNomura, D.; Delille, Bruno ; Dieckmann, G.S. et alConference (2014, March)There seems little doubt that sea ice is permeable to CO2 and other gases although air–sea ice gas flux is more or less inhibited at a brine volume fraction of less than 5% representing the threshold for ... [more ▼]There seems little doubt that sea ice is permeable to CO2 and other gases although air–sea ice gas flux is more or less inhibited at a brine volume fraction of less than 5% representing the threshold for fluid permeability of sea ice. Generally, air–sea ice CO2 flux is at its minimum in winter due to low sea ice temperatures and consequently reduced permeability despite the fact the partial pressure of CO2 in sea ice is usually high at that time and sea ice has therefore the potential to release CO2 to the atmosphere. Here, we present first evidence that snow laden Antarctic sea ice can act as source for atmospheric CO2 even during mid-winter and early spring. During a mid-winter cruise to the Weddell Sea (AWECS, 2013) and an early spring cruise off east Antarctica (SIPEX-2, 2012), due to thick insulating snow covers, the bottom of the snow and the surface of the sea ice were relatively warm (>–10°C) even though air temperature was sometimes below –30°C. In addition, in both areas, sea ice was characterized by high bulk-salinities, resulting in brine volume fractions that are generally higher than 5%. Automatic “open-closed” chamber measurements indicated positive CO2 fluxes of up to +2.5 mmol C m–2 day–1, illustrating that sea ice acted as a source of atmospheric CO2. Higher fluxes were measured at bare ice surfaces after removing the snow. However, generally low snow densities (mean: 339 kg m–3), indicating a permeable snow cover, facilitated degassing of CO2 at the snow-air interface. Our results therefore suggest that even in the winter and early spring, Antarctic sea ice can act as CO2 source for the atmosphere, particularly in areas with a thick insulating snow cover. [less ▲]Detailed reference viewed: 110 (1 ULg) Year Round survey of Ocean-Sea Ice-Air Exchanges – the YROSIAE surveyDelille, Bruno ; Haskell, T.; Champenois, Willy et alConference (2014, March)YROSIAE survey aimed to carry out a year-round survey of land-fast sea ice focusing on the study of sea ice physics and biogeochemistry in order to a) better understand and budget exchanges of energy and ... [more ▼]YROSIAE survey aimed to carry out a year-round survey of land-fast sea ice focusing on the study of sea ice physics and biogeochemistry in order to a) better understand and budget exchanges of energy and matter across the ocean-sea ice-atmosphere interfaces during sea ice growth and decay and b) quantify their potential impact on fluxes of climate gases (CO2, DMS, CH4, N2O) to the atmosphere and on carbon and macro- nutrients and micro-nutrients export to the ocean. Ice cores, sea water, brines and exported material were collected at regular intervals about 1 km off cape Evans from November 2011 to December 2011 and from September 2012 to December 2012 in trace-metal clean conditions. Samples are processed to characterize both the vertical distribution and temporal changes of climate gases (CO2, DMS, CH4, N2O), CO2-related parameters (dissolved inorganic carbon, total alkalinity and CaCO3 amount), physical parameters (salinity, temperature, texture, 18O), biogeochemical parameters (macro-nutrients, particulate and dissolved organic carbon, δ13C, δ30Si and δ15N, micro-nutrients - including iron) and biological parameters ( chlorophyll a, primary production within sea ice derived from O2:Ar and O2:N ratios, autotrophic species determination, bacterial cell counts a.s.o.). In addition, we deployed a micro-meterological tower and automatic chambers to measure air-ice CO2 fluxes. Continuous measurements of ice temperature and ice accretion or melting, both at the ice-ocean and the ice-atmosphere interfaces were provided by an “Ice-T” ice mass balance buoy. Sediment traps collected particles below the ice between 10 and 70 m, while dust collectors provided a record of a full suite of trace metal and dust at different levels above the ground. We will present the aims, overall approach and sampling strategy of the YROSIAE survey. In addition we will also discuss CO2 dynamics within the ice and present temporal air-ice CO2 fluxes over the year. We will provide a first budget of air-ice CO2 fluxes during ice growth for Antarctica sea ice and discuss the impact of the snow cover on air-ice CO2 fluxes. [less ▲]Detailed reference viewed: 123 (9 ULg) On the use of O2/Ar and O2/N2 to estimate the biological carbon uptake in landfast sea iceZhou, Jiayun ; Delille, Bruno ; Brabant, F. et alPoster (2014, March)Sea ice is one of the largest biomes on Earth. The net community production (NCP) of the microorganisms living in sea ice impacts the dynamics of pCO2 in sea ice, and therefore the CO2 exchanges at the ... [more ▼]Sea ice is one of the largest biomes on Earth. The net community production (NCP) of the microorganisms living in sea ice impacts the dynamics of pCO2 in sea ice, and therefore the CO2 exchanges at the air-ice-sea interfaces. As oxygen O2 and carbon C are both involved in the photosynthetic and respiration processes, one can theoretically assess NCP (in terms of C uptake) from O2 measurements. However, the concentration of O2 in sea ice depends not only on biological processes (i.e., NCP) but also on physical processes. We present a technique for assessing NCP in sea ice, based on the use of the O2/Ar ratio, which should correct for the physical contribution in O2 variations. We also compare the use of O2/Ar and O2/N2 for deriving NCP, and demonstrate that O2/Ar is more suitable, as it is more sensitive and less affected by gas diffusion and gas bubble formation during sea ice growth and decay than O2/N2. Using O2/Ar, we then provide conservative estimates of NCP in landfast sea ice, from ice cores collected in Barrow, from January through June 2009. The minimum estimate of the NCP in the whole ice cover reached 229 mg C.m-².d-1 in late spring. This is about 20 times higher than the atmospheric C uptake at that time identified from CO2 fluxes measurements at the ice-air interface, and therefore indicates that the main source of C used in the NCP was from the under-ice water. [less ▲]Detailed reference viewed: 59 (1 ULg) Factors driving pCO2 dynamics in sea ice during a large-scale ice tank experimentZhou, Jiayun ; Delille, Bruno ; Tison, J.-L. et alConference (2014, March)According to previous studies, pCO2 fluxes measured over Arctic sea ice are higher than those measured over Antarctic sea ice. We hypothesized that this was due to enhanced respiration in Arctic sea ice ... [more ▼]According to previous studies, pCO2 fluxes measured over Arctic sea ice are higher than those measured over Antarctic sea ice. We hypothesized that this was due to enhanced respiration in Arctic sea ice, as a consequence of higher riverine inputs of dissolved organic carbon (DOC) into Arctic seawater. We tested this hypothesis during the Interice V experiment at the HSVA (Hamburg) environmental test basin facility. We reproduced the growth and decay cycle of sea ice in replicate mesocosms (1 m3) filled with North Sea water (NSW series), and compared these with another series of mesocosms to which humic-rich river water had been added (10%) to increase the DOC concentration (R series). Primary producers were excluded from the experiment. The evolution of the temperature, salinity, DOC, pCO2 and bacterial biomass and production were measured in ice sampled at regular intervals throughout the experiment, as well as in the under-ice water. In addition, ice-air pCO2 fluxes were continuously monitored over both NSW and R mesocosms. pCO2 values in ice were higher in the R ice than in the NSW ice. This is attributed to the DOC content and bacterial respiration, rather than to the ice physical properties (i.e., ice permeability constrained by the ice temperature and salinity). Indeed, R ice had higher DOC content and bacterial production than the NSW ice while both showed similar physical properties. The evolution of the ice-air pCO2 fluxes was consistent with the evolution of pCO2 in ice. The fluxes were, as expected, positive (from sea ice to the atmosphere) during ice growth and negative (from the atmosphere to the ice) during ice melt. [less ▲]Detailed reference viewed: 90 (4 ULg) Biological and physical controls on DMS,P dynamics in ice-shelf-influenced fast iceCarnat, G.; Zhou, Jiayun ; Papakyriakou, T. et alConference (2014, March)Dimethylsulfide (DMS) is a volatile sulphur compound produced by the degradation of dimethylsulphoniopropionate (DMSP), a metabolite synthesized by microalgae as i.a. cryoprotectant and osmoregulator. It ... [more ▼]Dimethylsulfide (DMS) is a volatile sulphur compound produced by the degradation of dimethylsulphoniopropionate (DMSP), a metabolite synthesized by microalgae as i.a. cryoprotectant and osmoregulator. It is also an important climate-active gas, being the primary source of marine-derived sulphate aerosols which play an important role in the earth-atmosphere radiation balance. In the last two decades, there has been an increasing interest in the role of the marine cryosphere in the DMS,P cycle, motivated by repeated observations of very high DMS,P concentrations in sea ice. However, our understanding of the factors driving the spatiotemporal variations of these high concentrations, and hence the fate of the sea ice DMS pool, remains limited. To date, studies have essentially focused on biotic factors, attributing the high DMS,P concentrations to the high biomass of the sympagic communities, and to their strong physiological response to the low temperature and high salinity stresses of the brine habitat. We present here an approach integrating both biotic and abiotic factors, as we investigate the influence of sea ice growth processes and brine dynamics on the DMS,P cycle. We focus on a fast ice site (Cape Evans, McMurdo Sound, Antarctica) under the influence of ice-shelf waters, and provide measurements covering a full cycle of ice growth. We show a good correspondence between isolated maxima of DMS,P in interior ice and the occurrence of platelet crystals in the ice texture. We develop the idea that platelet ice formation in May strongly modifies the production of DMS,P by (1) favoring the incorporation of strong DMSP producers and by (2) exposing these producers to stronger environmental stresses. We then show the influence of the development and decline of a strong diatom bloom from October to November on bottom ice DMS,P concentrations. Finally, we show that the increase in brine volume fraction (permeability) on warming in early December triggers (1) an important release of DMS to the ocean through brine convection, and (2) a vertical redistribution of DMSP across the ice. [less ▲]Detailed reference viewed: 103 (3 ULg) Using stable isotopes to unravel the role of sea-ice in the methane cycleSapart, C.J.; Zhou, Jiayun ; Niemann, T et alPoster (2014, March)Methane (CH4) plays an important role in the Earth’s climate system. The atmospheric CH4 concentration has increased in concert with the industrialization, but since the mid 80’s the CH4 growth rate ... [more ▼]Methane (CH4) plays an important role in the Earth’s climate system. The atmospheric CH4 concentration has increased in concert with the industrialization, but since the mid 80’s the CH4 growth rate decreased to reach a near-zero level in 2000 and started to increase again from 2007 on. However, the underlying variations in sources and/or sinks that cause these variations are to date not well understood. To predict future climate, it is essential to unravel the processes controlling the CH4 cycle, especially in the Arctic regions, which are highly vulnerable to climate change and contain large CH4 reservoirs. Recently, an unexpected CH4 excess has been reported above Arctic sea-ice showing that sea-ice might play a significant role in the CH4 cycle. Nonetheless, the nature of the process leading to CH4 production in or nearby sea-ice has not yet been identified. We applied a new multi-proxy approach merging atmospheric chemistry, glaciology and biogeochemistry to understand and quantify the processes responsible for the CH4 excess above sea-ice. We performed CH4 isotope (13C and D) analyses on sea-ice samples, as well as microbial (lipid biomarkers) and geochemical measurements, to determine the possible pathways involved in CH4 production and removal in or nearby sea-ice. We will present results from sea-ice samples drilled above the shallow-shelf in Barrow (Alaska) from January to June 2009 as well as above deep Southern Ocean locations in 2013. Those results allow investigating the seasonality and spatial variability in methane formation and removal pathways associated to the methane enclosed in sea-ice. [less ▲]Detailed reference viewed: 96 (1 ULg) Dimethyl sulfide and dimethylsulfoniopropionate profiles in sea ice during winter in the Weddell SeaUhlig, C.; Tison, J.-L.; Rintala, J. et alConference (2014, March)This study presents profiles of the organic sulphur components dimethylsulfide (DMS) and dimethylsulfoniopropionate (DMSP) in sea ice cores collected during the AWECS (Antarctic Winter Ecosytem Climate ... [more ▼]This study presents profiles of the organic sulphur components dimethylsulfide (DMS) and dimethylsulfoniopropionate (DMSP) in sea ice cores collected during the AWECS (Antarctic Winter Ecosytem Climate Study) cruise on RV Polarstern (ANT29-6) in the Weddell Sea. DMS is a semi-volatile sulfur component and under discussion to be climate active, as its oxidation products might act as cloud condensation nuclei - thus cooling the atmosphere. It is produced by enzymatic cleavage of the precursor DMSP, which is synthesized by various types of phytoplankton and serves for example as compatible solute and cryoprotectant. Due to the physico-chemical conditions given, i.e. the high salinity and the icy matrix, sea ice as habitat favors production of high levels of DMSP by the inhabiting microalgae. DMSP and DMS are frequently found in high concentrations in sea ice during spring and summer. The aim of this study was to investigate DMS(P) levels in winter sea ice as data for the winter season is yet scarce, but is of importance for global budgeting. Preliminary results of our study show that DMS(P) production in sea ice in the Weddell Sea is also significant during winter. This stands in contrast to previous measurements in Arctic winter sea ice (CFL-IPY cruise in the Circumpolar Flaw Lead Polynya), where DMS(P) concentrations were very low. Possible explanations for the differences between DMS(P) levels in the Arctic and Antarctic might be the different snow cover and thus insulation, light regimes and also microbial community structure within the ice. DMS(P) levels were generally correlated with chlorophyll a concentrations, although the details are complex and seem to be influenced by species composition and species specific DMSP/Chla ratios. The DMS profiles mirrored the permeability of the sea ice following DMSP in the impermeable areas while showing losses to the ice surface and ice-water interface in the more permeable regions. Winter DMS(P) profiles are furthermore compared to data collected during the following spring cruise of RV Polarstern (ANT29-7) in the Weddell Sea. [less ▲]Detailed reference viewed: 72 (2 ULg) Land-fast sea ice of McMurdo Sound as a source of bio-essential trace metals for primary productivity in the Ross Sea, AntarcticaSchoemann, V.; de Jong, J.T.M.; Tison, J.L. et alConference (2014, March)Iron (Fe) is an essential micronutrient. Its low abundance limits primary productivity in more than 30% of the oceans, including the Southern Ocean, and has a crucial impact on the biogeochemical cycles ... [more ▼]Iron (Fe) is an essential micronutrient. Its low abundance limits primary productivity in more than 30% of the oceans, including the Southern Ocean, and has a crucial impact on the biogeochemical cycles of carbon and other elements with ultimate influence on the Earth climate system. Other trace metals, like Mn, Zn, Co and Cu are also required for microorganisms cell metabolism and may be (co-) limiting. Previous data on dissolved and particulate Fe concentration data showed that Fe is 10-100 times more concentrated in the sea ice than in underlying seawater and that sea ice melt can deliver up to 70% of the daily Fe supply to the surface waters. According to budget estimates in East Antarctica and in the Weddell Sea, accumulated Fe would largely derive from the underlying seawater rather than from atmospheric inputs. Most of the available data of trace metals in the sea ice concern pack ice and Fe. Only very scarce data exist on land-fast ice and on other trace metal concentrations. In this presentation, the general objective is to assess the role of land-fast ice as a source of Fe and other bio-essential trace metals (e.g. Mn, Zn, Cu, Mo, Cd), its impact on primary productivity and on the biological pump. Samples of sea ice, brines and seawater as well as dusts samples have been collected during the land-based sampling program YROSIAE at Cape Evans (Scott Base, McMurdo Sound, Ross Sea, Antarctica) from Nov 2011 to Dec 2011 and from Aug 2012 to Dec 2012. Dissolved and particulate trace metals concentrations have been measured by a recently developed method, which combines multiple element isotope dilution with preconcentration using the Nobias Chelate PA1 resin and ICP-MS analysis. Concentrations of trace metals in snow collected during the present study are one to up to five orders of magnitude higher than the concentrations previously observed in snow from East Antarctica, showing a much stronger dust input of these metals in McMurdo Sound. When comparing the concentrations obtained in the under-ice seawater with those obtained in the snow at McMurdo Sound, concentrations of Fe, Al, Mn, Co are much lower, whereas concentrations of Cu, Zn and Pb are similar and the concentrations of Ni, Mo and Cd are higher. Inventories of these trace metals in the land-fast sea ice give insights on its role as a source of bio-essential trace metal for the fuelling of the seasonal Ross Sea bloom. Other sources of these trace metals will be addressed and compared. [less ▲]Detailed reference viewed: 161 (7 ULg) Modelling argon dynamics in first-year sea iceMoreau, S.; Vancoppenolle, M; Zhou, Jiayun et alin Ocean Modelling (2014), 73Abstract: Focusing on physical processes, we aim at constraining the dynamics of argon (Ar), a biogeochemically inert gas, within first year sea ice, using observation data and a one-dimensional halo ... [more ▼]Abstract: Focusing on physical processes, we aim at constraining the dynamics of argon (Ar), a biogeochemically inert gas, within first year sea ice, using observation data and a one-dimensional halo-thermodynamic sea ice model, including parameterization of gas physics. The incorporation and transport of dissolved Ar within sea ice and its rejection via gas-enriched brine drainage to the ocean, are modeled following fluid transport equations through sea ice. Gas bubbles nucleate within sea ice when Ar is above saturation and when the total partial pressure of all three major atmospheric gases (N2, O2 and Ar) is above the brine hydrostatic pressure. The uplift of gas bubbles due to buoyancy is allowed when the brine network is connected with a brine volume above a given threshold. Ice-atmosphere Ar fluxes are formulated as a diffusive process proportional to the differential partial pressure of Ar between brine inclusions and the atmosphere. Two simulations corresponding to two case studies that took place at Point Barrow (Alaska, 2009) and during an ice-tank experiment (INTERICE IV, Hamburg, Germany, 2009) are presented. Basal entrapment and vertical transport due to brine motion enable a qualitatively sound representation of the vertical profile of the total Ar (i.e. the Ar dissolved in brine inclusions and contained in gas bubbles; TAr). Sensitivity analyses suggest that gas bubble nucleation and rise are of most importance to describe gas dynamics within sea ice. Ice-atmosphere Ar fluxes and the associated parameters do not drastically change the simulated TAr. Ar dynamics are dominated by uptake, transport by brine dynamics and bubble nucleation in winter and early spring; and by an intense and rapid release of gas bubbles to the atmosphere in spring. Important physical processes driving gas dynamics in sea ice are identified, pointing to the need for further field and experimental studies. [less ▲]Detailed reference viewed: 50 (5 ULg) Physical and biological controls on DMS,P dynamics in ice-shelf influenced fast ice during a winter-spring and a spring-summer transitionsCarnat, G.; Zhou, Jiayun ; Papakyriakou, T. et alin Journal of Geophysical Research. Oceans (2014), 119We report the seasonal and vertical variations of dimethylsulphide (DMS) and its precursor dimethylsulfoniopropionate (DMSP) in fast ice at Cape Evans, McMurdo Sound (Antarctica) during the spring-summer ... [more ▼]We report the seasonal and vertical variations of dimethylsulphide (DMS) and its precursor dimethylsulfoniopropionate (DMSP) in fast ice at Cape Evans, McMurdo Sound (Antarctica) during the spring-summer transition in 2011 and winter-spring transition in 2012. We compare the variations of DMS,P observed to the seasonal evolution of the ice algal biomass and of the physical properties of the ice cover, with emphasis on the ice texture and brine dynamics. Isolated DMS and DMSP maxima were found during both seasonal episodes in interior ice and corresponded to the occurrence of platelet crystals in the ice texture. We show that platelet crystals formation corresponded in time and depth to the incorporation of dinoflagellates (strong DMSP producers) in the ice cover. We also show that platelet crystals could modify the environmental stresses on algal cells and perturb the vertical redistribution of DMS,P concentrations. We show that during the winter-spring transition in 2012, the DMS,P profiles were strongly influenced by the development and decline of a diatom dominated bloom in the bottom ice, with DMSP variations remarkably following chl a variations. During the spring-summer transition in 2011, the increase in brine volume fraction (influencing ice permeability) on warming was shown to trigger (1) an important release of DMS to the under-ice water through brine convection (2) a vertical redistribution of DMSP across the ice [less ▲]Detailed reference viewed: 35 (3 ULg) Southern Ocean CO2 sink: The contribution of the sea iceDelille, Bruno ; Vancoppenolle, M; Geilfus, N.-X. et alin Journal of Geophysical Research. Oceans (2014), 119We report first direct measurements of the partial pressure of CO2 (pCO2) within Antarctic pack sea ice brines and related CO2 fluxes across the air-ice interface. From late winter to summer, brines ... [more ▼]We report first direct measurements of the partial pressure of CO2 (pCO2) within Antarctic pack sea ice brines and related CO2 fluxes across the air-ice interface. From late winter to summer, brines encased in the ice change from a CO2 large over-saturation, relative to the atmosphere, to a marked under-saturation while the underlying oceanic waters remains slightly oversaturated. The decrease from winter to summer of pCO2 in the brines is driven by dilution with melting ice, dissolution of carbonate minerals crystals and net primary production. As the ice warms, its permeability increases, allowing CO2 transfer at the air-sea ice interface. The sea ice changes from a transient source to a sink for atmospheric CO2. We upscale these observations to the whole Antarctic sea-icesea ice cover using the NEMO-LIM3 large-scale sea ice-ocean, and provide first estimates of spring and summer CO2 uptake from the atmosphere by Antarctic sea ice. Over the spring-summer period, the Antarctic sea-icesea ice cover is a net sink of atmospheric CO2 of 0.029 PgC, about 58% of the estimated annual uptake from the Southern Ocean. Sea ice then contributes significantly to the sink of CO2 of the Southern Ocean. [less ▲]Detailed reference viewed: 82 (15 ULg) Sea ice pCO2 dynamics and air–ice CO2 fluxes during the Sea Ice Mass Balance in the Antarctic (SIMBA) experiment – Bellingshausen Sea, AntarcticaGeilfus, N.-X.; Tison, J.-L.; Ackley, S. F. et alin Cryosphere (The) (2014), 8(6), 2395--2407Temporal evolution of pCO2 profiles in sea ice in the Bellingshausen Sea, Antarctica, in October 2007 shows physical and thermodynamic processes controls theCO2 sys- tem in the ice. During the survey ... [more ▼]Temporal evolution of pCO2 profiles in sea ice in the Bellingshausen Sea, Antarctica, in October 2007 shows physical and thermodynamic processes controls theCO2 sys- tem in the ice. During the survey, cyclical warming and cool- ing strongly influenced the physical, chemical, and thermo- dynamic properties of the ice cover. Two sampling sites with contrasting characteristics of ice and snow thickness were sampled: one had little snow accumulation (from 8 to 25 cm) and larger temperature and salinity variations than the sec- ond site, where the snow cover was up to 38 cm thick and therefore better insulated the underlying sea ice. We show that each cooling/warming event was associated with an in- crease/decrease in the brine salinity, total alkalinity (TA), to- tal dissolved inorganic carbon (TCO2), and in situ brine and bulk ice CO2 partial pressures (pCO2). Thicker snow covers reduced the amplitude of these changes: snow cover influ- ences the sea ice carbonate system by modulating the temper- ature and therefore the salinity of the sea ice cover. Results indicate that pCO2 was undersaturated with respect to the at- mosphere both in the in situ bulk ice (from 10 to 193 µatm) and brine (from 65 to 293 µatm), causing the sea ice to act as a sink for atmospheric CO2 (up to 2.9mmolm−2 d−1), despite supersaturation of the underlying seawater (up to 462 µatm) [less ▲]Detailed reference viewed: 108 (2 ULg) CO2 and CH4 in sea ice from a subarctic fjord under influence of riverine inputCrabeck, O.; Delille, Bruno ; Thomas, David et alin Biogeosciences (2014), 11(23), 6525--6538We present the CH4 concentration [CH4], the par- tial pressure of CO2 (pCO2) and the total gas content in bulk sea ice from subarctic, land-fast sea ice in the Kapisillit fjord, Greenland. Fjord systems ... [more ▼]We present the CH4 concentration [CH4], the par- tial pressure of CO2 (pCO2) and the total gas content in bulk sea ice from subarctic, land-fast sea ice in the Kapisillit fjord, Greenland. Fjord systems are characterized by freshwater runoff and riverine input and based on $\delta$18O data, we show that >30\% of the surface water originated from periodic river input during ice growth. This resulted in fresher sea-ice layers with higher gas content than is typical from marine sea ice. The bulk ice [CH4] ranged from 1.8 to 12.1 nmolL−1, which corresponds to a partial pressure ranging from 3 to 28ppmv. This is markedly higher than the average atmo- spheric methane content of 1.9ppmv. Evidently most of the trapped methane within the icewas contained inside bubbles, and only a minor portion was dissolved in the brines. The bulk ice pCO2 ranged from 60 to 330ppmv indicating that sea ice at temperatures above −4 ◦C is undersaturated com- pared to the atmosphere (390 ppmv). This study adds to the few existing studies of CH4 and CO2 in sea ice, and we con- clude that subarctic seawater can be a sink for atmospheric CO2, while being a net source of CH4. [less ▲]Detailed reference viewed: 67 (0 ULg) First ‘in situ’ determination of gas transport coefficients (DO2, DAr and DN2 ) from bulk gas 2 concentration measurements (O2, N2, Ar) in natural sea iceCrabeck, O.; Delille, Bruno ; Rysgaard, S. et alin Journal of Geophysical Research. Oceans (2014), 119We report bulk gas concentrations of O2, N2 and Ar, as well as their transport coefficients, in natural landfast subarctic sea ice in southwest Greenland. The observed bulk ice gas composition was 27.5 ... [more ▼]We report bulk gas concentrations of O2, N2 and Ar, as well as their transport coefficients, in natural landfast subarctic sea ice in southwest Greenland. The observed bulk ice gas composition was 27.5% O2, 71.4% N2 and 1.09% Ar. Most previous studies suggest that convective transport is the main driver of gas displacement in sea ice and have neglected diffusion processes. According to our data, brines were stratified within the ice, so that no convective transport could occur within the brine system. Therefore, diffusive transport was the main driver of gas migration. By analysing the temporal evolution of an internal gas peak within the ice, we deduced the bulk gas transport coefficients for oxygen (DO2), argon (DAr) and nitrogen (DN222 ). The values fit to the few existing estimates from experimental work, and are close to the diffusivity values in water (10-5 cm2 s-124 ). We suggest that gas bubbles escaping from the brine to the atmosphere - as the ice gets more permeable during melt could be responsible for the previously reported high transport coefficients. These results underline that when there is no convective transport within the sea ice, the transport of gas by diffusion through the brines, either in the liquid or gaseous phases, is a major factor in controlling the ocean–atmosphere exchange. [less ▲]Detailed reference viewed: 16 (0 ULg) Insights into oxygen transport and net community production in sea ice from oxygen, nitrogen and argon concentrationsZhou, Jiayun ; Delille, Bruno ; Brabant, F. et alin Biogeosciences (2014), 11We present the evolution of O2 standing stocks, saturation levels and concentrations in landfast sea ice, collected in Barrow (Alaska), from February to June 2009. The comparison of the standing stocks ... [more ▼]We present the evolution of O2 standing stocks, saturation levels and concentrations in landfast sea ice, collected in Barrow (Alaska), from February to June 2009. The comparison of the standing stocks and saturation levels of O2 against those of N2 and Ar suggests that the dynamic of O2 in sea ice strongly depends on physical processes (gas incorporation and subsequent transport). We then discuss on the use of O2 / Ar and O2 / N2 to correct for the physical contribution and to determine the biological contribution (NCP) to O2 supersaturations. We conclude that O2 / Ar suits better than O2 / N2, because O2 / N2 is more sensitive due to the relative abundance of O2, N2 and Ar, and less biased when gas bubble formation and gas diffusion are maximized. We further estimate the NCP in the impermeable layers during ice growth and in the permeable layers during ice decay. Our results indicate that NCP contributed to a~release of carbon to the atmosphere in the upper ice layers, but to an uptake of carbon at sea ice bottom. Overall, seawater (rather than the atmosphere) may be the main supplier of carbon for sea ice microorganisms. [less ▲]Detailed reference viewed: 36 (7 ULg)