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  • 11
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    Svalbard 2010 team (2010): EPOCA Svalbard mesocosm experiment 2010 depth-integrated (0-12m) variables (2013)
    PANGAEA
    Details
    Publication Date: 2024-03-15
    Keywords: 19-Butanoyloxyfucoxanthin; 1-Iodoethane; 1-Iodopropane; 2-Iodopropane; Algae, biomass as carbon; Algae, fatty acids; Algae abundance; Alkaline phosphatase; Alkalinity, Gran titration (Gran, 1950); Alkalinity, total; Alloxanthin; alpha-Carotene, beta,epsilon-Carotene; Ammonium; Aphanizophyll; Aragonite saturation state; Arctic; Bacteria; Bacteria, biomass as carbon; Bacteria, fatty acids; Bacteria, high DNA fluorescence; Bacteria, low DNA fluorescence; Bacterial/community respiration, oxygen, ratio; Bacterial biomass production of carbon; Bacterial biomass production of carbon, standard deviation; Bacterial production; Bacterial production, standard deviation; beta-Carotene, beta,beta-Carotene; Bicarbonate ion; BIOACID; Biogenic silica; Biological Impacts of Ocean Acidification; Biomass/Abundance/Elemental composition; Bromochloromethane; Bromoiodomethane; Calanus finmarchicus, δ13C; Calcite saturation state; Calculated; Calculated from linear regression; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, particulate; Carbon, organic, dissolved; Carbon, organic, particulate; Carbon, total, particulate; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, flux per mesocosm; Chloroiodomethane; Chlorophyll a; Chlorophyll a, areal concentration; Chlorophyll b; Chlorophyll c1+c2; Chlorophyll c3; Chlorophytes; Cirripedia, larvae, δ13C; Coast and continental shelf; Community composition and diversity; Coulometry; Cryptophytes; Cyanobacteria, biomass per area; DATE/TIME; delta 13C labeling method; Diadinoxanthin; Diatoxanthin; Dibromochloromethane; Dibromomethane; Diiodomethane; Dimethyl sulfide, dissolved; Dimethylsulfoniopropionate; Entire community; EPOCA; EUR-OCEANS; European network of excellence for Ocean Ecosystems Analysis; European Project on Ocean Acidification; Exudation as determined by 14C DOC production; Exudation as determined by 14C DOC production, standard deviation; Field experiment; Flow cytometry; Fucoxanthin; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Gas chromatography - Mass spectrometry (GC-MS); GC-PFPD; Gross community production of oxygen; Hand-operated CTD (Sea&Sun Technology, CTD 60M); High Performance Liquid Chromatography (HPLC); Identification; Iodomethane; Kongsfjorden-mesocosm; MESO; Mesocosm experiment; Mesocosm or benthocosm; Myxoxanthophyll; Nanoplankton; Neoxanthin; Net community production, standard deviation; Net community production of carbon dioxide; Net community production of oxygen; Nitrate; Nitrite; Nitrogen, organic, dissolved; Nitrogen, organic, particulate; Nitrous oxide; OA-ICC; Ocean Acidification International Coordination Centre; Other metabolic rates; Oxygen; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; Peridinin; pH; Phosphate; Phosphorus, organic, dissolved; Phosphorus, organic, particulate; Phytoplankton, biomass per area; Picophytoplankton; Polar; Prasinoxanthin; Primary production/Photosynthesis; Primary production of POC as determined by 14C POC production; Primary production of POC as determined by 14C POC production, standard deviation; Pulsed flame photometric detector - gas chromatography; Respiration; Respiration, oxygen, bacterial; Respiration, oxygen, bacterial, standard error; Respiration, oxygen, community; Respiration, oxygen, community, standard error; Salinity; Sample comment; Sigmas; Silicon; Svalbard; Temperature, water; Thymidine incorporation; Time, incubation; Transfer velocity, carbon dioxide; Transfer velocity, dimethyl sulfide; Transfer velocity, nitrous oxide; Tribromomethane; Turbidity (Formazin Turbidity Unit); Violaxanthin; Viral abundance; Virus/bacteria ratio; Viruses; Water content of mesocosm; Zeaxanthin; Δδ13C; δ13C, algae; δ13C, bacteria; δ13C, dissolved inorganic carbon; δ13C, dissolved organic carbon; δ13C, particulate organic carbon
    Type: Dataset
    Format: text/tab-separated-values, 35076 data points
    Location Call Number Limitation Availability
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    DATA PANGAEA
  • 12
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    Seawater carbonate chemistry and size-fractionated bacterial protein production (BPP) of free-living and particle associated bacteria and abundance of particle associated heterotrophic prokaryotes of KOSMOS Finland 2012 mesocosm study (2017)
    PANGAEA
    Details
    Publication Date: 2024-03-15
    Keywords: Alkalinity, total; Aragonite saturation state; Baltic Sea; Bicarbonate ion; BIOACID; Biological Impacts of Ocean Acidification; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Coast and continental shelf; DATE/TIME; Day of experiment; Entire community; Field experiment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); KOSMOS_2012_Tvaerminne; MESO; Mesocosm experiment; Mesocosm label; Mesocosm or benthocosm; OA-ICC; Ocean Acidification International Coordination Centre; Other metabolic rates; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; Prokaryotes, heterotroph, particle associated; Protein production, free-living bacteria; Protein production, particle associated bacteria; Salinity; SOPRAN; Surface Ocean Processes in the Anthropocene; Temperate; Temperature, water
    Type: Dataset
    Format: text/tab-separated-values, 2122 data points
    Location Call Number Limitation Availability
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    DATA PANGAEA
  • 13
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    Alterations in microbial community composition with increasing fCO2: a mesocosm study in the eastern Baltic Sea (2017)
    Copernicus Publications (EGU)
    In:  Biogeosciences (BG), 14 (16). pp. 3831-3849.
    Details
    Publication Date: 2020-02-06
    Description: Ocean acidification resulting from the uptake of anthropogenic carbon dioxide (CO2) by the ocean is considered a major threat to marine ecosystems. Here we examined the effects of ocean acidification on microbial community dynamics in the eastern Baltic Sea during the summer of 2012 when inorganic nitrogen and phosphorus were strongly depleted. Large-volume in situ mesocosms were employed to mimic present, future and far future CO2 scenarios. All six groups of phytoplankton enumerated by flow cytometry ( 〈  20 µm cell diameter) showed distinct trends in net growth and abundance with CO2 enrichment. The picoeukaryotic phytoplankton groups Pico-I and Pico-II displayed enhanced abundances, whilst Pico-III, Synechococcus and the nanoeukaryotic phytoplankton groups were negatively affected by elevated fugacity of CO2 (fCO2). Specifically, the numerically dominant eukaryote, Pico-I, demonstrated increases in gross growth rate with increasing fCO2 sufficient to double its abundance. The dynamics of the prokaryote community closely followed trends in total algal biomass despite differential effects of fCO2 on algal groups. Similarly, viral abundances corresponded to prokaryotic host population dynamics. Viral lysis and grazing were both important in controlling microbial abundances. Overall our results point to a shift, with increasing fCO2, towards a more regenerative system with production dominated by small picoeukaryotic phytoplankton.
    Type: Article , PeerReviewed
    Format: text
    Format: text
    DOI: 10.5194/bg-14-3831-2017
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    OceanRep: Article in a Scientific Journal - peer-reviewed
  • 14
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    Effect of ocean acidification and elevated fCO2 on trace gas production by a Baltic Sea summer phytoplankton community (2016)
    Copernicus Publications (EGU)
    In:  Biogeosciences (BG), 13 . pp. 4595-4613.
    Details
    Publication Date: 2019-09-23
    Description: The Baltic Sea is a unique environment as the largest body of brackish water in the world. Acidification of the surface oceans due to absorption of anthropogenic CO2 emissions is an additional stressor facing the pelagic community of the already challenging Baltic Sea. To investigate its impact on trace gas biogeochemistry, a large-scale mesocosm experiment was performed off Tvärminne Research Station, Finland, in summer 2012. During the second half of the experiment, dimethylsulfide (DMS) concentrations in the highest-fCO2 mesocosms (1075–1333 µatm) were 34 % lower than at ambient CO2 (350 µatm). However, the net production (as measured by concentration change) of seven halocarbons analysed was not significantly affected by even the highest CO2 levels after 5 weeks' exposure. Methyl iodide (CH3I) and diiodomethane (CH2I2) showed 15 and 57 % increases in mean mesocosm concentration (3.8 ± 0.6 increasing to 4.3 ± 0.4 pmol L−1 and 87.4 ± 14.9 increasing to 134.4 ± 24.1 pmol L−1 respectively) during Phase II of the experiment, which were unrelated to CO2 and corresponded to 30 % lower Chl a concentrations compared to Phase I. No other iodocarbons increased or showed a peak, with mean chloroiodomethane (CH2ClI) concentrations measured at 5.3 (±0.9) pmol L−1 and iodoethane (C2H5I) at 0.5 (±0.1) pmol L−1. Of the concentrations of bromoform (CHBr3; mean 88.1 ± 13.2 pmol L−1), dibromomethane (CH2Br2; mean 5.3 ± 0.8 pmol L−1), and dibromochloromethane (CHBr2Cl, mean 3.0 ± 0.5 pmol L−1), only CH2Br2 showed a decrease of 17 % between Phases I and II, with CHBr3 and CHBr2Cl showing similar mean concentrations in both phases. Outside the mesocosms, an upwelling event was responsible for bringing colder, high-CO2, low-pH water to the surface starting on day t16 of the experiment; this variable CO2 system with frequent upwelling events implies that the community of the Baltic Sea is acclimated to regular significant declines in pH caused by up to 800 µatm fCO2. After this upwelling, DMS concentrations declined, but halocarbon concentrations remained similar or increased compared to measurements prior to the change in conditions. Based on our findings, with future acidification of Baltic Sea waters, biogenic halocarbon emissions are likely to remain at similar values to today; however, emissions of biogenic sulfur could significantly decrease in this region.
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
    Format: text
    Format: text
    DOI: 10.5194/bg-13-4595-2016
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    OceanRep: Article in a Scientific Journal - peer-reviewed
  • 15
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    Ocean acidification impacts bacteria–phytoplankton coupling at low-nutrient conditions (2017)
    Copernicus Publications (EGU)
    In:  Biogeosciences (BG), 14 . pp. 1-15.
    Details
    Publication Date: 2021-04-23
    Description: The oceans absorb about a quarter of the annually produced anthropogenic atmospheric carbon dioxide (CO2), resulting in a decrease in surface water pH, a process termed ocean acidification (OA). Surprisingly little is known about how OA affects the physiology of heterotrophic bacteria or the coupling of heterotrophic bacteria to phytoplankton when nutrients are limited. Previous experiments were, for the most part, undertaken during productive phases or following nutrient additions designed to stimulate algal blooms. Therefore, we performed an in situ large-volume mesocosm ( ∼  55 m3) experiment in the Baltic Sea by simulating different fugacities of CO2 (fCO2) extending from present to future conditions. The study was conducted in July–August after the nominal spring bloom, in order to maintain low-nutrient conditions throughout the experiment. This resulted in phytoplankton communities dominated by small-sized functional groups (picophytoplankton). There was no consistent fCO2-induced effect on bacterial protein production (BPP), cell-specific BPP (csBPP) or biovolumes (BVs) of either free-living (FL) or particle-associated (PA) heterotrophic bacteria, when considered as individual components (univariate analyses). Permutational Multivariate Analysis of Variance (PERMANOVA) revealed a significant effect of the fCO2 treatment on entire assemblages of dissolved and particulate nutrients, metabolic parameters and the bacteria–phytoplankton community. However, distance-based linear modelling only identified fCO2 as a factor explaining the variability observed amongst the microbial community composition, but not for explaining variability within the metabolic parameters. This suggests that fCO2 impacts on microbial metabolic parameters occurred indirectly through varying physicochemical parameters and microbial species composition. Cluster analyses examining the co-occurrence of different functional groups of bacteria and phytoplankton further revealed a separation of the four fCO2-treated mesocosms from both control mesocosms, indicating that complex trophic interactions might be altered in a future acidified ocean. Possible consequences for nutrient cycling and carbon export are still largely unknown, in particular in a nutrient-limited ocean.
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
    Format: text
    Format: text
    DOI: 10.5194/bg-14-1-2017
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    OceanRep: Article in a Scientific Journal - peer-reviewed
  • 16
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    Effects of ocean acidification on pelagic carbon fluxes in a mesocosm experiment (2016)
    Copernicus Publications (EGU)
    In:  Biogeosciences (BG), 13 . pp. 6081-6093.
    Details
    Publication Date: 2021-04-23
    Description: About a quarter of anthropogenic CO2 emissions are currently taken up by the oceans, decreasing seawater pH. We performed a mesocosm experiment in the Baltic Sea in order to investigate the consequences of increasing CO2 levels on pelagic carbon fluxes. A gradient of different CO2 scenarios, ranging from ambient ( ∼  370 µatm) to high ( ∼  1200 µatm), were set up in mesocosm bags ( ∼  55 m3). We determined standing stocks and temporal changes of total particulate carbon (TPC), dissolved organic carbon (DOC), dissolved inorganic carbon (DIC), and particulate organic carbon (POC) of specific plankton groups. We also measured carbon flux via CO2 exchange with the atmosphere and sedimentation (export), and biological rate measurements of primary production, bacterial production, and total respiration. The experiment lasted for 44 days and was divided into three different phases (I: t0–t16; II: t17–t30; III: t31–t43). Pools of TPC, DOC, and DIC were approximately 420, 7200, and 25 200 mmol C m−2 at the start of the experiment, and the initial CO2 additions increased the DIC pool by  ∼  7 % in the highest CO2 treatment. Overall, there was a decrease in TPC and increase of DOC over the course of the experiment. The decrease in TPC was lower, and increase in DOC higher, in treatments with added CO2. During phase I the estimated gross primary production (GPP) was  ∼  100 mmol C m−2 day−1, from which 75–95 % was respired,  ∼  1 % ended up in the TPC (including export), and 5–25 % was added to the DOC pool. During phase II, the respiration loss increased to  ∼  100 % of GPP at the ambient CO2 concentration, whereas respiration was lower (85–95 % of GPP) in the highest CO2 treatment. Bacterial production was  ∼  30 % lower, on average, at the highest CO2 concentration than in the controls during phases II and III. This resulted in a higher accumulation of DOC and lower reduction in the TPC pool in the elevated CO2 treatments at the end of phase II extending throughout phase III. The “extra” organic carbon at high CO2 remained fixed in an increasing biomass of small-sized plankton and in the DOC pool, and did not transfer into large, sinking aggregates. Our results revealed a clear effect of increasing CO2 on the carbon budget and mineralization, in particular under nutrient limited conditions. Lower carbon loss processes (respiration and bacterial remineralization) at elevated CO2 levels resulted in higher TPC and DOC pools than ambient CO2 concentration. These results highlight the importance of addressing not only net changes in carbon standing stocks but also carbon fluxes and budgets to better disentangle the effects of ocean acidification.
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
    Format: text
    DOI: 10.5194/bg-13-6081-2016
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    OceanRep: Article in a Scientific Journal - peer-reviewed
  • 17
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    Interactive effects of light, CO2 and iron on Antarctic phytoplankton growth and physiology (2019)
    In:  EPIC3IMBeR Future Oceans2 Conference, Brest, France, 2019-06
    Details
    Publication Date: 2019-06-26
    Repository Name: EPIC Alfred Wegener Institut
    Type: Conference , notRev
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    PAPER (OA)
  • 18
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    Marine environmental effects of Saharan dust deposition in the tropical North Atlantic Ocean. (2018)
    In:  EPIC3DICE Workshop: The Role of Dust in Climate Change: A biogeochemistry perspective., Las curces, Chile., 2018-01-08-2018-01-10
    Details
    Publication Date: 2018-01-09
    Repository Name: EPIC Alfred Wegener Institut
    Type: Conference , notRev
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    PAPER (OA)
  • 19
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    Variability and change in the west Antarctic Peninsula marine system: research priorities and opportunities (2019)
    PERGAMON-ELSEVIER SCIENCE LTD
    In:  EPIC3Progress In Oceanography, PERGAMON-ELSEVIER SCIENCE LTD, 173, pp. 208-237, ISSN: 0079-6611
    Details
    Publication Date: 2019-04-26
    Description: The west Antarctic Peninsula (WAP) region has undergone significant changes in temperature and seasonal ice dynamics since the mid-twentieth century, with strong impacts on the regional ecosystem, ocean chemistry and hydrographic properties. Changes to these long-term trends of warming and sea ice decline have been observed in the 21st century, but their consequences for ocean physics, chemistry and the ecology of the high-productivity shelf ecosystem are yet to be fully established. The WAP shelf is important for regional krill stocks and higher trophic levels, whilst the degree of variability and change in the physical environment and documented biological and biogeochemical responses make this a model system for how climate and sea ice changes might restructure high-latitude ecosystems. Although this region is arguably the best-measured and best-understood shelf region around Antarctica, significant gaps remain in spatial and temporal data capable of resolving the atmosphere-ice-ocean-ecosystem feedbacks that control the dynamics and evolution of this complex polar system. Here we summarise the current state of knowledge regarding the key mechanisms and interactions regulating the physical, biogeochemical and biological processes at work, the ways in which the shelf environment is changing, and the ecosystem response to the changes underway. We outline the overarching cross-disciplinary priorities for future research, as well as the most important discipline-specific objectives. Underpinning these priorities and objectives is the need to better-define the causes, magnitude and timescales of variability and change at all levels of the system. A combination of traditional and innovative approaches will be critical to addressing these priorities and developing a co-ordinated observing system for the WAP shelf, which is required to detect and elucidate change into the future.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Format: application/pdf
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    PAPER (OA)
  • 20
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    Alterations in microbial community composition with increasing fCO2: a mesocosm study in the eastern Baltic Sea (2017)
    In:  EPIC3Biogeosciences, 14(16), pp. 3831-3849, ISSN: 1726-4189
    Details
    Publication Date: 2017-09-06
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Format: application/pdf
    Location Call Number Limitation Availability
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    PAPER (OA)
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