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  • 2010-2014  (736,956)
  • 1980-1984  (12)
  • 2014  (736,956)
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  • 1
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    PANGAEA
    In:  Supplement to: Kottmeier, Dorothee; Rokitta, Sebastian D; Tortell, Philippe Daniel; Rost, Björn (2014): Strong shift from HCO3- to CO2 uptake in Emiliania huxleyi with acidification: new approach unravels acclimation versus short-term pH effects. Photosynthesis Research, 121(2-3), 265-275, https://doi.org/10.1007/s11120-014-9984-9
    Publication Date: 2024-05-22
    Description: Effects of ocean acidification on Emiliania huxleyi strain RCC 1216 (calcifying, diploid life-cycle stage) and RCC 1217 (non-calcifying, haploid life-cycle stage) were investigated by measuring growth, elemental composition, and production rates under different pCO2 levels (380 and 950 µatm). In these differently acclimated cells, the photosynthetic carbon source was assessed by a (14)C disequilibrium assay, conducted over a range of ecologically relevant pH values (7.9-8.7). In agreement with previous studies, we observed decreased calcification and stimulated biomass production in diploid cells under high pCO2, but no CO2-dependent changes in biomass production for haploid cells. In both life-cycle stages, the relative contributions of CO2 and HCO3 (-) uptake depended strongly on the assay pH. At pH values =〈 8.1, cells preferentially used CO2 (〉= 90 % CO2), whereas at pH values 〉= 8.3, cells progressively increased the fraction of HCO3 (-) uptake (~45 % CO2 at pH 8.7 in diploid cells; ~55 % CO2 at pH 8.5 in haploid cells). In contrast to the short-term effect of the assay pH, the pCO2 acclimation history had no significant effect on the carbon uptake behavior. A numerical sensitivity study confirmed that the pH-modification in the (14)C disequilibrium method yields reliable results, provided that model parameters (e.g., pH, temperature) are kept within typical measurement uncertainties. Our results demonstrate a high plasticity of E. huxleyi to rapidly adjust carbon acquisition to the external carbon supply and/or pH, and provide an explanation for the paradoxical observation of high CO2 sensitivity despite the apparently high HCO3 (-) usage seen in previous studies.
    Keywords: Alkalinity, total; Aragonite saturation state; Bicarbonate ion; Biomass/Abundance/Elemental composition; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, organic, particulate, per cell; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Carbon dioxide usage fraction; Chlorophyll a per cell; Chromista; Emiliania huxleyi; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; Haptophyta; Irradiance; Laboratory experiment; Laboratory strains; Light:Dark cycle; Nitrogen, organic, particulate, per cell; North Atlantic; OA-ICC; Ocean Acidification International Coordination Centre; Other metabolic rates; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; Phosphate; Phytoplankton; Potentiometric; Potentiometric titration; Pressure, water; Salinity; Silicate; Single species; Species; Strain; Temperature, water; Total particulate carbon per cell; Treatment
    Type: Dataset
    Format: text/tab-separated-values, 548 data points
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  • 2
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    PANGAEA
    In:  Supplement to: Lohbeck, Kai T; Riebesell, Ulf; Reusch, Thorsten B H (2014): Gene expression changes in the coccolithophore Emiliania huxleyi after 500 generations of selection to ocean acidification. Proceedings of the Royal Society B-Biological Sciences, 281(1786), 20140003-20140003, https://doi.org/10.1098/rspb.2014.0003
    Publication Date: 2024-05-22
    Description: Coccolithophores are unicellular marine algae that produce biogenic calcite scales and substantially contribute to marine primary production and carbon export to the deep ocean. Ongoing ocean acidification particularly impairs calcifying organisms, mostly resulting in decreased growth and calcification. Recent studies revealed that the immediate physiological response in the coccolithophore Emiliania huxleyi to ocean acidification may be partially compensated by evolutionary adaptation, yet the underlying molecular mechanisms are currently unknown. Here, we report on the expression levels of 10 candidate genes putatively relevant to pH regulation, carbon transport, calcification and photosynthesis in E. huxleyi populations short-term exposed to ocean acidification conditions after acclimation (physiological response) and after 500 generations of high CO2 adaptation (adaptive response). The physiological response revealed downregulation of candidate genes, well reflecting the concomitant decrease of growth and calcification. In the adaptive response, putative pH regulation and carbon transport genes were up-regulated, matching partial restoration of growth and calcification in high CO2-adapted populations. Adaptation to ocean acidification in E. huxleyi likely involved improved cellular pH regulation, presumably indirectly affecting calcification. Adaptive evolution may thus have the potential to partially restore cellular pH regulatory capacity and thereby mitigate adverse effects of ocean acidification.
    Keywords: Alkalinity, total; Aragonite saturation state; Bicarbonate ion; BIOACID; Biological Impacts of Ocean Acidification; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Chromista; Emiliania huxleyi; Experiment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Gene expression (incl. proteomics); Gene name; Haptophyta; Laboratory experiment; Laboratory strains; Not applicable; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; Phosphate; Phytoplankton; Salinity; Sample code/label; Single species; Species; Temperature, water; Threshold cycle, quantitative polymerase chain reaction; Treatment
    Type: Dataset
    Format: text/tab-separated-values, 15400 data points
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  • 3
    Publication Date: 2024-05-22
    Keywords: AA; Ammonium; Autoanalyzer; Calculated from mass/volume; Carbon, organic, total; Carbon/Nitrogen ratio; Chlorophyll a per unit sediment mass; Core; Density, wet bulk; Depth, bottom/max; DEPTH, sediment/rock; Depth, top/min; Dry sieving + wet pipetting; Element analyser CHN; Grain size, mean; Hand push corer; HSR; HYT; Hythe, Colne estuary; Kurtosis; Nitrate and Nitrite; Nitrite; Nitrogen, total; Phaeopigments per unit sediment mass; Porosity, fractional; Skewness; Sorting; SPEC; Spectrophotometer; Tide; Water content, wet mass
    Type: Dataset
    Format: text/tab-separated-values, 903 data points
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  • 4
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    PANGAEA
    In:  Supplement to: Sperfeld, Erik; Mangor‑Jensen, Anders; Dalpadado, Padmini (2014): Effect of increasing sea water pCO2 on the northern Atlantic krill species Nyctiphanes couchii. Marine Biology, 161(10), 2359-2370, https://doi.org/10.1007/s00227-014-2511-x
    Publication Date: 2024-05-22
    Description: Surprisingly little is known about potential effects of ocean acidification on krill of the Northern Hemisphere as ecologically very important food web component. Sub-adult individuals of the northern Atlantic krill species Nyctiphanes couchii (caught at Austevoll near Bergen, Norway, in January 2013) were exposed in the laboratory to four different levels of pCO2 (430, 800, 1,100, and 1,700 µatm) for 5 weeks in order to assess potential changes in a set of biological response variables. Survival decreased and the frequency of moulting-related deaths increased with increasing pCO2. Survival was considerably reduced at relatively high pCO2 of 1,700 µatm and tended to be negatively affected at 1,100 µatm pCO2. However, the experimental results show no significant effects of pCO2 on inter-moult period and growth at pCO2 levels below 1,100 µatm. No differences in length measurements of the carapace and uropod were observed across pCO2 levels, indicating no effect of changing carbonate chemistry on the morphology of those calciferous parts of the exoskeleton. The results suggest that sub-adult N. couchii may not suffer dramatically from predicted near-future changes in pCO2. However, potential detrimental effects on the moulting process and associated higher mortality at 1,100 µatm pCO2 cannot be excluded. Further experiments are needed in order to investigate whether early life stages of N. couchii show a different sensitivity to elevated sea water pCO2 and whether those results are transferable to other krill species of the Northern Hemisphere.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Animalia; Aragonite saturation state; Aragonite saturation state, standard deviation; Arthropoda; Bergen_fjord; Bicarbonate ion; Bicarbonate ion, standard deviation; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calcite saturation state, standard deviation; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carapace, length; Carapace width; Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbonate ion; Carbonate ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, standard deviation; Coast and continental shelf; Coulometric titration; Diameter; Duration, number of days; EXP; Experiment; Figure; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth rate; Growth rate, standard deviation; Individuals; Laboratory experiment; Length; Mortality/Survival; North Atlantic; Nyctiphanes couchii; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; pH, standard deviation; Phosphate; Phosphate, standard deviation; Potentiometric titration; Salinity; Salinity, standard deviation; Silicate; Silicate, standard deviation; Single species; Species; Spectrophotometric; Survival; Survival rate, standard error; Table; Temperate; Temperature, water; Temperature, water, standard deviation; Time, standard deviation; Time in days; Zooplankton
    Type: Dataset
    Format: text/tab-separated-values, 9602 data points
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  • 5
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    PANGAEA
    In:  Supplement to: Van de Waal, Dedmer B; Eberlein, Tim; John, Uwe; Wohlrab, Sylke; Rost, Björn (2014): Impact of elevated pCO2 on paralytic shellfish poisoning toxin content and composition in Alexandrium tamarense. Toxicon, 78, 58-67, https://doi.org/10.1016/j.toxicon.2013.11.011
    Publication Date: 2024-05-22
    Description: Ocean acidification is considered a major threat to marine ecosystems and may particularly affect primary producers. Here we investigated the impact of elevated pCO2 on paralytic shellfish poisoning toxin (PST) content and composition in two strains of Alexandrium tamarense, Alex5 and Alex2. Experiments were carried out as dilute batch to keep carbonate chemistry unaltered over time. We observed only minor changes with respect to growth and elemental composition in response to elevated pCO2. For both strains, the cellular PST content, and in particular the associated cellular toxicity, was lower in the high CO2 treatments. In addition, Alex5 showed a shift in its PST composition from a nonsulfated analogue towards less toxic sulfated analogues with increasing pCO2. Transcriptomic analyses suggest that the ability of A. tamarense to maintain cellular homeostasis is predominantly regulated on the post-translational level rather than on the transcriptomic level. Furthermore, genes associated to secondary metabolite and amino acid metabolism in Alex5 were down-regulated in the high CO2 treatment, which may explain the lower PST content. Elevated pCO2 also induced up-regulation of a putative sulfotransferase sxtN homologue and a substantial down-regulation of several sulfatases. Such changes in sulfur metabolism may explain the shift in PST composition towards more sulfated analogues. All in all, our results indicate that elevated pCO2 will have minor consequences for growth and elemental composition, but may potentially reduce the cellular toxicity of A. tamarense.
    Keywords: Alexandrium tamarense; Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Bicarbonate ion; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbon, organic, particulate, per cell; Carbon, organic, particulate, standard deviation; Carbon/Nitrogen ratio; Carbon/Nitrogen ratio, standard deviation; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Category; Cell density; Cellular paralytic shellfish toxin, total; Cellular paralytic shellfish toxin, total, standard deviation; Chromista; Coulometric titration; Di-sulfated toxins C1+C2; Di-sulfated toxins C1+C2, standard deviation; Figure; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Gene abundance; Gene expression (incl. proteomics); Gonyautoxins 1/4; Gonyautoxins 1/4, standard deviation; Gonyautoxins 2/3; Gonyautoxins 2/3, standard deviation; Growth/Morphology; Growth rate; Growth rate, standard deviation; Immunology/Self-protection; Laboratory experiment; Laboratory strains; Myzozoa; Neosaxitoxin; Neosaxitoxin, standard deviation; Neurotoxin saxitoxin; Neurotoxin saxitoxin, standard deviation; Nitrogen, organic, particulate, per cell; Nitrogen, organic, particulate, standard deviation; Not applicable; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Particulate organic carbon, production, standard deviation; Particulate organic carbon production per cell; Pelagos; pH; pH, standard deviation; Phosphate; Phytoplankton; Potentiometric; Potentiometric titration; Primary production/Photosynthesis; Salinity; Single species; Species; Strain; Table; Temperature, water; Time in days; Toxicity, cellular; Toxicity, cellular, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 6500 data points
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  • 6
    Publication Date: 2024-05-22
    Keywords: AA; Ammonium; Autoanalyzer; BLS; Brightlingsea, Colne estuary; Calculated from mass/volume; Carbon, organic, total; Carbon/Nitrogen ratio; Chlorophyll a per unit sediment mass; Core; Density, wet bulk; Depth, bottom/max; DEPTH, sediment/rock; Depth, top/min; Dry sieving + wet pipetting; Element analyser CHN; Grain size, mean; Hand push corer; HSR; Kurtosis; Nitrate and Nitrite; Nitrite; Nitrogen, total; Phaeopigments per unit sediment mass; Porosity, fractional; Skewness; Sorting; SPEC; Spectrophotometer; Tide; Water content, wet mass
    Type: Dataset
    Format: text/tab-separated-values, 901 data points
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  • 7
    Publication Date: 2024-05-22
    Keywords: AA; ALF; Alresford, Colne estuary; Ammonium; Autoanalyzer; Calculated from mass/volume; Carbon, organic, total; Carbon/Nitrogen ratio; Chlorophyll a per unit sediment mass; Core; Density, wet bulk; Depth, bottom/max; DEPTH, sediment/rock; Depth, top/min; Dry sieving + wet pipetting; Element analyser CHN; Grain size, mean; Hand push corer; HSR; Kurtosis; Nitrate and Nitrite; Nitrite; Nitrogen, total; Phaeopigments per unit sediment mass; Porosity, fractional; Skewness; Sorting; SPEC; Spectrophotometer; Tide; Water content, wet mass
    Type: Dataset
    Format: text/tab-separated-values, 897 data points
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  • 8
    Publication Date: 2024-05-22
    Keywords: Bottle number; Carbon, organic, total; Climate - Biogeochemistry Interactions in the Tropical Ocean; CTD; CTD/Rosette; CTD1; CTD11; CTD12; CTD13; CTD14; CTD15; CTD16; CTD17; CTD18; CTD19; CTD2; CTD20; CTD21; CTD22; CTD23; CTD24; CTD25; CTD26; CTD28; CTD29; CTD30; CTD31; CTD32; CTD33; CTD34; CTD35; CTD36; CTD37; CTD38; CTD39; CTD4; CTD40; CTD41; CTD42; CTD43; CTD44; CTD45; CTD46; CTD47; CTD48; CTD49; CTD5; CTD50; CTD51; CTD52; CTD53; CTD54; CTD55; CTD56; CTD57; CTD58; CTD59; CTD6; CTD60; CTD61; CTD62; CTD63; CTD64; CTD65; CTD66; CTD67; CTD68; CTD69; CTD7; CTD70; CTD9; CTD-RO; Date/Time of event; DEPTH, water; Event label; Freon-12 (dichlorodifluoromethane); LATITUDE; LONGITUDE; Nitrate; Nitrite; Nitrogen, total; Nitrous oxide; Optional event label; Oxygen; Phosphate; POS347; POS347_112-1; POS347_113-1; POS347_114-1; POS347_114-2; POS347_115-1; POS347_115-2; POS347_117-1; POS347_119-1; POS347_120-1; POS347_121-1; POS347_122-1; POS347_123-1; POS347_124-1; POS347_125-1; POS347_126-1; POS347_127-1; POS347_128-1; POS347_129-1; POS347_130-1; POS347_131-1; POS347_132-1; POS347_133-1; POS347_134-1; POS347_136-1; POS347_137-1; POS347_138-1; POS347_139-1; POS347_140-1; POS347_141-1; POS347_142-1; POS347_143-1; POS347_144-1; POS347_145-1; POS347_146-1; POS347_147-1; POS347_148-1; POS347_148-2; POS347_149-1; POS347_150-1; POS347_150-2; POS347_151-1; POS347_152-1; POS347_153-1; POS347_153-2; POS347_154-1; POS347_155-1; POS347_156-1; POS347_156-2; POS347_157-1; POS347_158-1; POS347_158-2; POS347_159-1; POS347_160-1; POS347_161-1; POS347_162-1; POS347_163-1; POS347_164-1; POS347_165-1; POS347_166-1; POS347_167-1; POS347_168-1; POS347_169-1; POS347_170-1; POS347_171-1; POS347_172-1; POS347_173-1; Poseidon; Pressure, water; Salinity; Sample code/label; SFB754; Silicate; SOPRAN; Sulfur hexafluoride, SF6; Surface Ocean Processes in the Anthropocene; Temperature, water; West Africa
    Type: Dataset
    Format: text/tab-separated-values, 5023 data points
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  • 9
    Publication Date: 2024-05-21
    Description: Abstract
    Description: A seismological experiment was started in July 2014 in and around the East Eifel Volcanic Field, Germany. Following two unusually deep micro-earthquakes in September 2013 (about 40 km depth) a seismic network was installed to record more local seismic events in order to better understand the seismicity and dynamics of this region. Ten recording stations of the GFZ GIPP (Geophysical Instrument Pool Potsdam at Helmholtz Centre Potsdam, GFZ German Research Centre for Geosciences) and three recording stations of the KIT KABBA (Karlsruhe BroadBand Array at Karlsruhe Institute of Technology) were placed between the permanent stations of the state earthquake survey (Landeserdbebendienst). Altogether about 18-20 short-period and broadband stations could be used to study the seismicity up to August 2016. This dataset is unique concerning the station density in this region and allows determination of hypocenter parameters with high precision and accuracy, estimation of the local crustal and upper mantle structure as well as using array techniques for wavelengths of about 10-50 km. After August 2016 the network was reconfigured and continuously updated by KIT-GPI and LGB. Waveform data is available from the GEOFON data centre, under network code 1P, and is fully open.
    Keywords: Monitoring system ; EARTH SCIENCE 〉 SOLID EARTH 〉 TECTONICS 〉 EARTHQUAKES ; EARTH SCIENCE 〉 SOLID EARTH 〉 TECTONICS 〉 VOLCANIC ACTIVITY ; In Situ/Laboratory Instruments 〉 Magnetic/Motion Sensors 〉 Seismometers ; In Situ Land-based Platforms 〉 GEOPHYSICAL STATIONS/NETWORKS ; In Situ Land-based Platforms 〉 GEOPHYSICAL STATIONS/NETWORKS 〉 SEISMOLOGICAL STATIONS ; Passive seismic ; Seismometers ; Velocity ; MiniSEED ; GIPP ; MESI
    Type: Dataset , Seismic Network
    Format: 235GB
    Format: .mseed
    Format: XML
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  • 10
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    Unknown
    GFZ Data Services
    Publication Date: 2024-05-21
    Description: Abstract
    Description: On 1st April, 23:46:50 UTC, an Mw 8.1 earthquake ruptured offshore northern Chile, near the town of Pisagua northwest of Iquique, followed one day later by a Mw7.6 event, both events in the centre of the Integrated Plate boundary Observatory Chile (IPOC). These earthquakes occurred within a seismic gap left behind by two great earthquakes devastating the northern Chilean and southern Peruvian coast about 140 years ago in 1868 and 1877. The segment inbetween, about 500 km long, was the only one along the Chilean subduction zone that has not ruptured within the last century. The earthquakes were recorded by the IPOC multi-parameter stations plus several additional off-line strong- and weak-motion instruments. A network of GPS monuments covering the onshore region deformed by the earthquake was measured just weeks before the event by GFZ scientists. Taking advantage of the long history of preceding work, presence of the permanent multi-parameter network and excellent knowledge of GFZ scientists of the region, a 20 short-period seismograph network was installed to complement the existing pre- and co-seismic data sets. This campaign was the first case for the „HAzard-Risk-Team (HART)“ initiative of GFZ. Stations operated from mid April 2014, i.e. shortly after the mainshock, to January 2016.
    Keywords: Monitoring system ; Seismological stations ; In Situ/Laboratory Instruments 〉 Magnetic/Motion Sensors 〉 Seismometers ; In Situ Land-based Platforms 〉 GEOPHYSICAL STATIONS/NETWORKS ; Passive seismic ; Seismometers ; Velocity ; MiniSEED ; GIPP ; MESI
    Type: Dataset , Seismic Network
    Format: 196GB
    Format: .mseed
    Format: XML
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