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  • 2010-2014  (50,811)
  • 1950-1954  (31)
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  • 1
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    Unknown
    PANGAEA
    In:  Supplement to: Bouimetarhan, Ilham; Prange, Matthias; Schefuß, Enno; Dupont, Lydie M; Lippold, Jörg; Mulitza, Stefan; Zonneveld, Karin A F (2012): Sahel megadrought during Heinrich Stadial 1: evidence for a three-phase evolution of the low- and mid-level West African wind system. Quaternary Science Reviews, 58, 66-76, https://doi.org/10.1016/j.quascirev.2012.10.015
    Publication Date: 2024-05-27
    Description: Millennial-scale dry events in the Northern Hemisphere monsoon regions during the last Glacial period are commonly attributed to southward shifts of the Intertropical Convergence Zone (ITCZ) associated with an intensification of the northeasterly (NE) trade wind system during intervals of reduced Atlantic meridional overturning circulation (AMOC). Through the use of high-resolution last deglaciation pollen records from the continental slope off Senegal, our data show that one of the longest and most extreme droughts in the western Sahel history, which occurred during the North Atlantic Heinrich Stadial 1 (HS1), displayed a succession of three major phases. These phases progressed from an interval of maximum pollen representation of Saharan elements between ~19 and 17.4 kyr BP indicating the onset of aridity and intensified NE trade winds, followed by a millennial interlude of reduced input of Saharan pollen and increased input of Sahelian pollen, to a final phase between ~16.2 and 15 kyr BP that was characterized by a second maximum of Saharan pollen abundances. This change in the pollen assemblage indicates a mid-HS1 interlude of NE trade wind relaxation, occurring between two distinct trade wind maxima, along with an intensified mid-tropospheric African Easterly Jet (AEJ) indicating a substantial change in West African atmospheric processes. The pollen data thus suggest that although the NE trades have weakened, the Sahel drought remained severe during this time interval. Therefore, a simple strengthening of trade winds and a southward shift of the West African monsoon trough alone cannot fully explain millennial-scale Sahel droughts during periods of AMOC weakening. Instead, we suggest that an intensification of the AEJ is needed to explain the persistence of the drought during HS1. Simulations with the Community Climate System Model indicate that an intensified AEJ during periods of reduced AMOC affected the North African climate by enhancing moisture divergence over the West African realm, thereby extending the Sahel drought for about 4000 years.
    Keywords: 293; Center for Marine Environmental Sciences; GeoB9508-5; Gravity corer (Kiel type); M65/1; MARUM; Meteor (1986); SL
    Type: Dataset
    Format: application/zip, 5 datasets
    Location Call Number Expected Availability
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  • 2
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    PANGAEA
    In:  Laboratoire d'Océanographie de Villefranche | Supplement to: Fiorini, Sarah; Middelburg, Jack J; Gattuso, Jean-Pierre (2011): Effects of elevated CO2 partial pressure and temperature on the coccolithophore Syracosphaera pulchra. Aquatic Microbial Ecology, 64(3), 221-232, https://doi.org/10.3354/ame01520
    Publication Date: 2024-05-27
    Description: The response of three coccolithophores (Emiliania huxleyi, Calcidiscus leptoporus and Syracosphaera pulchra) to elevated partial pressure (pCO2) of carbon dioxide was investigated in batch cultures. For the first time, we also report on the response of the non calcifying (haploid) life stage of these three species. The growth rate, cell size, inorganic (PIC) and organic carbon (POC) of both life stages were measured at two different pCO2 (400and 760 ppm) and their organic and inorganic carbon production calculated. The two lifestages within the same species generally exhibited a similar response to elevated pCO2, theresponse of the haploid stage being often more pronounced than that of the diploid stage. Thegrowth rate was consistently higher at higher pCO2 but the response of other processes varied among species. The calcification rate of C. leptoporus and of S. pulchra did not change at elevated pCO2 while increased in E. huxleyi. The POC production as well as the cell size of both life stages of S. pulchra and of the haploid stage of E. huxleyi markedly decreased at elevated pCO2. It remained unaltered in the diploid stage of E. huxleyi and C. leptoporus and increased in the haploid stage of the latter. The PIC:POC ratio increased in E. huxleyi and was constant in C. leptoporus and S. pulchra. These results suggest that the non-calcifying stage, is more responsive than the calcifying stage and that the most versatile genera will proliferate in a more acidic ocean rather than all coccolithophores will decline.
    Keywords: Alkalinity, Gran titration (Gran, 1950); Alkalinity, total; Aragonite saturation state; Bicarbonate ion; Biomass/Abundance/Elemental composition; Bottles or small containers/Aquaria (〈20 L); Calcidiscus leptoporus; Calcification/Dissolution; Calcite saturation state; Calculated; Calculated, see reference(s); Calculated using seacarb; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, particulate, per cell; Carbon, organic, particulate; Carbon, organic, particulate, per cell; Carbon, total, particulate; Carbon, total, particulate, per cell; Carbon, total, particulate, production per cell; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Chromista; Coulter Counter (Beckman Coulter); Emiliania huxleyi; EPOCA; EUR-OCEANS; European network of excellence for Ocean Ecosystems Analysis; European Project on Ocean Acidification; Experimental treatment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; Haptophyta; Laboratory experiment; Laboratory strains; Light:Dark cycle; Mass spectrometer Thermo Electron Flash EA 1122 Analyzer; Measured; Mediterranean Sea; Nitrogen; Nitrogen, total; Nitrogen per cell; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; pH meter (Metrohm electrodes); Phytoplankton; Primary production/Photosynthesis; Radiation, photosynthetically active; Salinity; Sample ID; Single species; Skalar AutoAnalyser; Species; Suspended particulate matter; Syracosphaera pulchra; Temperature; Temperature, water; Transparent exopolymer particles; Transparent exopolymer particles per cell
    Type: Dataset
    Format: text/tab-separated-values, 1536 data points
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  • 3
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    PANGAEA
    In:  Supplement to: Fiorini, Sarah; Middelburg, Jack J; Gattuso, Jean-Pierre (2011): Testing the effects of elevated pCO2 on coccolithophores (Prymnesiophyceae): comparison between haploid and diploid life stages. Journal of Phycology, 47(6), 1281–1291, https://doi.org/10.1111/j.1529-8817.2011.01080.x
    Publication Date: 2024-05-27
    Description: The response of Emiliania huxleyi (Lohmann) W. W. Hay et H. Mohler, Calcidiscus leptoporus (G. Murray et V. H. Blackman) J. Schiller, andSyracosphaera pulchra Lohmann to elevated partial pressure of carbon dioxide (pCO2) was investigated in batch cultures. We reported on the response of both haploid and diploid life stages of these three species. Growth rate, cell size, particulate inorganic carbon (PIC), and particulate organic carbon (POC) of both life stages were measured at two different pCO2 (400 and 760 parts per million [ppm]), and their organic and inorganic carbon production were calculated. The two life stages within the same species generally exhibited a similar response to elevated pCO2, the response of the haploid stage being often more pronounced than that of the diploid stage. The growth rate was consistently higher at elevated pCO2, but the response of other processes varied among species. Calcification rate of C. leptoporusand of S. pulchra did not change at elevated pCO2, whereas it increased in E. huxleyi. POC production and cell size of both life stages of S. pulchra and of the haploid stage of E. huxleyi markedly decreased at elevated pCO2. It remained unaltered in the diploid stage of E. huxleyi and C. leptoporus and increased in the haploid stage of the latter. The PIC:POC ratio increased in E. huxleyi and was constant in C. leptoporus and S. pulchra. Elevated pCO2 has a significant effect on these three coccolithophore species, the haploid stage being more sensitive. This effect must be taken into account when predicting the fate of coccolithophores in the future ocean.
    Keywords: Alkalinity, Gran titration (Gran, 1950); Alkalinity, total; Aragonite saturation state; Bicarbonate ion; Biomass/Abundance/Elemental composition; Bottles or small containers/Aquaria (〈20 L); Calcidiscus leptoporus; Calcidiscus leptoporus, standard deviation; Calcification/Dissolution; Calcite saturation state; Calculated; Calculated using seacarb; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, particulate, per cell; Carbon, inorganic, particulate, production per cell; Carbon, organic, particulate, per cell; Carbon, organic, particulate, production per cell; Carbon/Nitrogen ratio; Carbon/Nitrogen ratio, standard deviation; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Chromista; Element analyser, Thermo Finnigan flash EA 1112; Emiliania huxleyi; Emiliania huxleyi, standard deviation; EPOCA; EUR-OCEANS; European network of excellence for Ocean Ecosystems Analysis; European Project on Ocean Acidification; Experimental treatment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; Growth rate, standard deviation; Haptophyta; Identification; Laboratory experiment; Laboratory strains; Lemaur hemocytometer (Fisher Scientific); Light:Dark cycle; Measured; Nitrate; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Particulate inorganic carbon, production, standard deviation; Particulate inorganic carbon/particulate organic carbon ratio; Particulate inorganic carbon/particulate organic carbon ratio, standard deviation; Particulate inorganic carbon per cell, standard deviation; Particulate organic carbon, production, standard deviation; Particulate organic carbon content per cell, standard deviation; Pelagos; pH; pH meter (Metrohm electrodes); Phosphate; Phytoplankton; Phytoplankton, cell biovolume; Phytoplankton, cell biovolume, standard deviation; Primary production/Photosynthesis; Radiation, photosynthetically active; Salinity; Single species; South Pacific; Species; Syracosphaera pulchra; Syracosphaera pulchra, standard deviation; Temperature, water
    Type: Dataset
    Format: text/tab-separated-values, 492 data points
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  • 4
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    PANGAEA
    In:  Supplement to: Dupont, Lydie M; Caley, Thibaut; Kim, Jung-Hyun; Castañeda, Isla S; Malaizé, Bruno; Giraudeau, Jacques (2011): Glacial-interglacial vegetation dynamics in South Eastern Africa coupled to sea surface temperature variations in the Western Indian Ocean. Climate of the Past, 7(4), 1209-1224, https://doi.org/10.5194/cp-7-1209-2011
    Publication Date: 2024-05-27
    Description: Glacial-interglacial fluctuations in the vegetation of South Africa might elucidate the climate system at the edge of the tropics between the Indian and Atlantic Oceans. However, vegetation records covering a full glacial cycle have only been published from the eastern South Atlantic. We present a pollen record of the marine core MD96-2048 retrieved by the Marion Dufresne from the Indian Ocean ~120 km south of the Limpopo River mouth. The sedimentation at the site is slow and continuous. The upper 6 m (spanning the past 342 Ka) have been analysed for pollen and spores at millennial resolution. The terrestrial pollen assemblages indicate that during interglacials, the vegetation of eastern South Africa and southern Mozambique largely consisted of evergreen and deciduous forests. During glacials open mountainous scrubland dominated. Montane forest with Podocarpus extended during humid periods was favoured by strong local insolation. Correlation with the sea surface temperature record of the same core indicates that the extension of mountainous scrubland primarily depends on sea surface temperatures of the Agulhas Current. Our record corroborates terrestrial evidence of the extension of open mountainous scrubland (including fynbos-like species of the high-altitude Grassland biome) for the last glacial as well as for other glacial periods of the past 300 Ka.
    Keywords: Acacia; Acalypha; Acanthaceae; Afraegle; Afrormosia; Afzelia; Age model; Aizoaceae; Alchornea; Alismataceae; Allophylus; Aloe-type; Amaranthaceae/Chenopodiaceae; Anemia-type; Anthoceros; Anthospermum; Artemisia (Africa); Avicennia; Balanites; Baphia-type; Blighia-type; Borassus-type; Borreria; Boscia-type; Brachystegia; Bridelia; Burkea; Butyrospermum; Buxus-type madagascaria; Caesalpinioideae; CALYPSO; Calypso Corer; Campanulaceae; Canthium; Caperonia; Capparis; Caryophyllaceae; Cassia-type; Casuarina; Celastraceae/Hippocrateaceae; Celtis; Center for Marine Environmental Sciences; Cephalosphaera; Chrysophyllum; Cissus; Clematis-type; Cleome; Cliffortia; Cnestis-type; Coffea-type; Cola cordifolia; Combretaceae/Melastomataceae; Commelinaceae; Commiphora; Compositae Liguliflorae; Compositae Tubuliflorae; Compositae Vernonieae; Cotula-type; Counting, palynology; Crossopteryx; Crotalaria; Croton-type; Cucumis; Cussonia; Cuviera; Cynometra-type; Cyperaceae (africa); Daisy-type; Daniellia-type; Deinbollia-type; DEPTH, sediment/rock; Dialium-type; Dicliptera-type; Diospyros; Dodonaea villosa; Dombeya-type; Dracaena; Elaeis guineensis; Erica (Africa); Erythrina; Euclea; Eugenia; Euphorbia; Euphorbiaceae undifferentiated; Evolvulus-type; Fadogia-type; Fagonia; Fern spores; Flabellaria; Gaertnera; Galium; Garcinia; Gazania-type; Grewia; Gunnera perpensa; Haplocoelum; Heritiera-type; Hermannia; Hymenocardia; Hyphaene; Hypoestes type; Ilex cf.. mitis; Indigofera-type; Isoberlinia-type; Justicia-type; Khaya; Kigelia-type; Klaineanthus; Lannea; Leea; Leonotis; Liliaceae; Limnophyton-type; Lobelia (Africa); Lonchocarpus; Lophira; Luffa; Lumnitzera racemosa; Lycopodium (Africa); Lycopodium cernuum; Macaranga; Mallotus; Manilkara; Marion Dufresne (1995); Marker, added; Marker, found; MARUM; MD104; MD96-2048; Melochia; Millettia; Mimosoideae; Mitragyna; Moraceae; Morelia senegalensis; Myrica; Myrsine africana; Nyctaginaceae; Nymphaea; Ochna; Ocimum; Olea; Ormocarpum; Oxygonum; Pandanus; Papilionoideae; Parinari; Passerina montana; PEGASE; Pelargonium; Peltophorum africanum; Pentabrachion-type reticulatum; Pentzia-type; Petalidium; Petersianthus macrocarpus; Phaeoceros; Phoenix; Piliostigma; Piptadeniastrum-type africanum; Plantago; Poaceae undifferentiated; Podocarpus; Pollen, total; Polycarpaea-type; Polygonum aviculare-type; Polygonum senegalense-type; Protea; Pseudolachnostylis-type; Psychotria; Psydrax-type subcordata; Pteris; Pterocarpus; Raphia; Rauvolfia; Restionaceae; Rhamnaceae; Rhizophora; Rhus-type; Rhynchosia-type; Rubiaceae monade; Ruellia; Rumex; Sapotaceae; Sapotaceae/Meliaceae; Scabiosa-type; Schefflera; Schrebera; Scrophulariaceae (Africa); Securinega; Selago-type; Solanum; Sorindeia-type juglandifolia; Spirostachys africana; Stephanocolporate striatoreticulate; Sterculia-type; Stereospermum; Stipularia africana; Stoebe-type; Strophanthus-type; Strychnos; Sutera-type; Tamarindus-type indica; Tapinanthus; Teclea-type; Tephrosia-type; Tetrorchidium; Thymelaeaceae; Tribulus; Trichilia; Typha angustifolia-type; Uapaca; Urticaceae; Volume; Waltheria; Zaluzianskya-type; Zanthoxylum; Ziziphus-type; Zygophyllum
    Type: Dataset
    Format: text/tab-separated-values, 24360 data points
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  • 5
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    PANGAEA
    In:  Supplement to: Rickaby, Rosalind E M; Henderiks, Jorijntje; Young, J N (2010): Perturbing phytoplankton: response and isotopic fractionation with changing carbonate chemistry in two coccolithophore species. Climate of the Past, 6(6), 771-785, https://doi.org/10.5194/cp-6-771-2010
    Publication Date: 2024-05-27
    Description: All species of coccolithophore appear to respond to perturbations of carbonate chemistry in a different way. Here, we show that the degree of malformation, growth rate and stable isotopic composition of organic matter and carbonate produced by two contrasting species of coccolithophore (Gephyrocapsa oceanica and Coccolithus pelagicus ssp. braarudii) are indicative of differences between their photosynthetic and calcification response to changing DIC levels (ranging from ~1100 to ~7800 µmol/kg) at constant pH (8.13 ± 0.02). Gephyrocapsa oceanica thrived under all conditions of DIC, showing evidence of increased growth rates at higher DIC, but C. braarudii was detrimentally affected at high DIC showing signs of malformation, and decreased growth rates. The carbon isotopic fractionation into organic matter and the coccoliths suggests that C. braarudii utilises a common internal pool of carbon for calcification and photosynthesis but G. oceanica relies on independent supplies for each process. All coccolithophores appear to utilize bicarbonate as their ultimate source of carbon for calcification resulting in the release of a proton. But, we suggest that this proton can be harnessed to enhance the supply of CO2(aq) for photosynthesis either from a large internal HCO3- pool which acts as a pH buffer (C. braarudii), or pumped externally to aid the diffusive supply of CO2 across the membrane from the abundant HCO3- (G. oceanica), likely mediated by an internal and external carbonic anhydrase respectively. Our simplified hypothetical spectrum of physiologies may provide a context to understand different species response to changing pH and DIC, the species-specific delta p and calcite "vital effects", as well as accounting for geological trends in coccolithophore cell size.
    Keywords: Alkalinity, total; Aragonite saturation state; Bicarbonate ion; Biomass/Abundance/Elemental composition; Bottles or small containers/Aquaria (〈20 L); Calcification/Dissolution; Calcite saturation state; Calculated, see reference(s); Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, particulate, per cell; Carbon, inorganic, particulate, production per cell; Carbon, organic, particulate; Carbon, organic, particulate, per cell; Carbon, organic, particulate, production per cell; Carbon, organic, particulate/Nitrogen, organic, particulate ratio; Carbon, total, particulate; Carbon, total, particulate, per cell; Carbon, total, particulate, production per cell; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Chromista; Coccolithus braarudii; Coccolithus braarudii, collapsed spheres; Coccolithus braarudii, intact spheres; Coccolithus braarudii, malformed; EPOCA; EUR-OCEANS; European network of excellence for Ocean Ecosystems Analysis; European Project on Ocean Acidification; Experimental treatment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Gephyrocapsa oceanica; Growth/Morphology; Growth rate; Haptophyta; Laboratory experiment; Laboratory strains; Light:Dark cycle; Mass spectrometer ANCA-SL 20-20 Europa Scientific; Mass spectrometer Finnigan Delta-S; Measured; Nitrogen, organic, particulate; Nitrogen, organic, particulate, per cell; Nitrogen, organic, particulate, production per cell; Not applicable; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Particulate inorganic carbon/particulate organic carbon ratio; Pelagos; pH; Phytoplankton; Primary production/Photosynthesis; Radiation, photosynthetically active; Salinity; Single species; Species; Temperature, water; δ13C, carbon dioxide, atmospheric; δ13C, dissolved inorganic carbon
    Type: Dataset
    Format: text/tab-separated-values, 1647 data points
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  • 6
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    PANGAEA
    In:  Supplement to: Borchard, Corinna; Borges, Alberto Vieira; Händel, Nicole; Engel, Anja (2011): Biogeochemical response of Emiliania huxleyi (PML B92/11) to elevated CO2 and temperature under phosphorous limitation: A chemostat study. Journal of Experimental Marine Biology and Ecology, 410, 61-71, https://doi.org/10.1016/j.jembe.2011.10.004
    Publication Date: 2024-05-27
    Description: The present study investigates the combined effect of phosphorous limitation, elevated partial pressure of CO2 (pCO2) and temperature on a calcifying strain of Emiliania huxleyi (PML B92/11) by means of a fully controlled continuous culture facility. Two levels of phosphorous limitation were consecutively applied by renewal of culture media (N:P = 26) at dilution rates (D) of 0.3 d- and 0.1 d-1. CO2 and temperature conditions were 300, 550 and 900 µatm pCO2 at 14 °C and 900 µatm pCO2 at 18 °C. In general, the steady state cell density and particulate organic carbon (POC) production increased with pCO2, yielding significantly higher concentrations in cultures grown at 900 µatm pCO2 compared to 300 and 550 µatm pCO2. At 900 µatm pCO2, elevation of temperature as expected for a greenhouse ocean, further increased cell densities and POC concentrations. In contrast to POC concentration, C-quotas (pmol C cell-1) were similar at D = 0.3 d-1 in all cultures. At D = 0.1 d-1, a reduction of C-quotas by up to 15% was observed in the 900 µatm pCO2 at 18 °C culture. As a result of growth rate reduction, POC:PON:POP ratios deviated strongly from the Redfield ratio, primarily due to an increase in POC. Ratios of particulate inorganic and organic carbon (PIC:POC) ranged from 0.14 to 0.18 at D = 0.3 d-1, and from 0.11 to 0.17 at D = 0.1 d-1, with variations primarily induced by the changes in POC. At D = 0.1 d-1, cell volume was reduced by up to 22% in cultures grown at 900 µatm pCO2. Our results indicate that changes in pCO2, temperature and phosphorus supply affect cell density, POC concentration and size of E. huxleyi (PML B92/11) to varying degrees, and will likely impact bloom development as well as biogeochemical cycling in a greenhouse ocean.
    Keywords: Alkalinity, total; Aragonite saturation state; Bicarbonate ion; Biomass/Abundance/Elemental composition; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calculated, see reference(s); Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, organic, particulate; Carbon, organic, particulate, production per cell; Carbon, organic, particulate/Nitrogen, organic, particulate ratio; Carbon, organic, particulate/Phosphorus, organic, particulate ratio; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Chromista; Colorimetry; Element analyser CNS, EURO EA; Emiliania huxleyi; EPOCA; EUR-OCEANS; European network of excellence for Ocean Ecosystems Analysis; European Project on Ocean Acidification; Experimental treatment; Experiment day; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Haptophyta; Infrared gas analyzer (LI-COR LI-6252); Laboratory experiment; Laboratory strains; Light:Dark cycle; Macro-nutrients; Measured; Nitrate; Nitrogen, inorganic, dissolved; Nitrogen, organic; Nitrogen, organic, particulate/Phosphorus, organic, particulate ratio; Not applicable; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Particulate organic carbon, per cell; Particulate organic carbon production; Particulate organic nitrogen per cell; Particulate organic nitrogen production; Particulate organic phosphorus per cell; Particulate organic phosphorus production; Pelagos; pH; Phosphate; Phosphorus, inorganic; Phosphorus, organic, particulate; Phosphorus, organic, particulate, production per cell; Phytoplankton; Primary production/Photosynthesis; Production of particulate organic nitrogen; Radiation, photosynthetically active; Revelle factor; Salinity; Salinometer - Tropic Marin Sea Salt, Dr. Biener GmbH, Germany; Sample ID; Single species; Spectrophotometry; Temperature; Temperature, water; WTW 340i pH-analyzer and WTW SenTix 81-electrode
    Type: Dataset
    Format: text/tab-separated-values, 1068 data points
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  • 7
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    PANGAEA
    In:  Supplement to: Lohbeck, Kai T; Riebesell, Ulf; Reusch, Thorsten B H (2012): Adaptive evolution of a key phytoplankton species to ocean acidification. Nature Geoscience, 5(5), 346-351, https://doi.org/10.1038/ngeo1441
    Publication Date: 2024-05-27
    Description: Ocean acidification, the drop in seawater pH associated with the ongoing enrichment of marine waters with carbon dioxide from fossil fuel burning, may seriously impair marine calcifying organisms. Our present understanding of the sensitivity of marine life to ocean acidification is based primarily on short-term experiments, in which organisms are exposed to increased concentrations of CO2. However, phytoplankton species with short generation times, in particular, may be able to respond to environmental alterations through adaptive evolution. Here, we examine the ability of the world's single most important calcifying organism, the coccolithophore Emiliania huxleyi, to evolve in response to ocean acidification in two 500-generation selection experiments. Specifically, we exposed E. huxleyi populations founded by single or multiple clones to increased concentrations of CO2. Around 500 asexual generations later we assessed their fitness. Compared with populations kept at ambient CO2 partial pressure, those selected at increased partial pressure exhibited higher growth rates, in both the single- and multiclone experiment, when tested under ocean acidification conditions. Calcification was partly restored: rates were lower under increased CO2 conditions in all cultures, but were up to 50% higher in adapted compared with non-adapted cultures. We suggest that contemporary evolution could help to maintain the functionality of microbial processes at the base of marine food webs in the face of global change.
    Keywords: Alkalinity, total; Aragonite saturation state; Bicarbonate ion; BIOACID; Biological Impacts of Ocean Acidification; Bottles or small containers/Aquaria (〈20 L); Calcification/Dissolution; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, particulate, per cell; Carbon, inorganic, particulate, production per cell; Carbon, organic, particulate, per cell; Carbon, organic, particulate, production per cell; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Cell size; Chromista; Emiliania huxleyi; Experiment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; 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); Particulate inorganic carbon/particulate organic carbon ratio; Pelagos; pH; Phosphate; Phytoplankton; Salinity; Single species; Species; Temperature, water; Treatment
    Type: Dataset
    Format: text/tab-separated-values, 3150 data points
    Location Call Number Expected Availability
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  • 8
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    PANGAEA
    In:  Supplement to: Bach, Lennart Thomas; Riebesell, Ulf; Schulz, Kai Georg (2011): Distinguishing between the effects of ocean acidification and ocean carbonation in the coccolithophore Emiliania huxleyi. Limnology and Oceanography, 56(6), 2040-2050, https://doi.org/10.4319/lo.2011.56.6.2040
    Publication Date: 2024-05-27
    Description: The coccolithophore Emiliania huxleyi was cultured under a broad range of carbonate chemistry conditions to distinguish the effects of individual carbonate system parameters on growth, primary production, and calcification. In the first experiment, alkalinity was kept constant and the fugacity of CO2(fCO2) varied from 2 to 600 Pa (1Pa ~ 10 µatm). In the second experiment, pH was kept constant (pHfree = 8) with fCO2 varying from 4 to 370 Pa. Results of the constant-alkalinity approach revealed physiological optima for growth, calcification, and organic carbon production at fCO2 values of ~20Pa, ~40 Pa, and ~80 Pa, respectively. Comparing this with the constant-pH approach showed that growth and organic carbon production increased similarly from low to intermediate CO2 levels but started to diverge towards higher CO2 levels. In the high CO2 range, growth rates and organic carbon production decreased steadily with declining pH at constant alkalinity while remaining consistently higher at constant pH. This suggests that growth and organic carbon production rates are directly related to CO2 at low (sub-saturating) concentrations, whereas towards higher CO2 levels they are adversely affected by the associated decrease in pH. A pH dependence at high fCO2 is also indicated for calcification rates, while the key carbonate system parameter determining calcification at low fCO2 remains unclear. These results imply that key metabolic processes in coccolithophores have their optima at different carbonate chemistry conditions and are influenced by different parameters of the carbonate system at both sides of the optimum.
    Keywords: Alkalinity, total; Aragonite saturation state; Bicarbonate ion; BIOACID; Biological Impacts of Ocean Acidification; Bottles or small containers/Aquaria (〈20 L); Calcification/Dissolution; Calcite saturation state; Calculated; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, particulate, production per cell; Carbon, organic, particulate, production per cell; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Chlorophyll a production per cell; Chromista; Emiliania huxleyi; Emiliania huxleyi, diameter; EPOCA; EUR-OCEANS; European network of excellence for Ocean Ecosystems Analysis; European Project on Ocean Acidification; Experimental treatment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Fugacity of carbon dioxide in seawater, standard deviation; Growth/Morphology; Growth rate; Haptophyta; Laboratory experiment; Laboratory strains; Light:Dark cycle; Measured; North Atlantic; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Particulate inorganic carbon/particulate organic carbon ratio; Pelagos; pH; Photometry; Phytoplankton; Pigments, Turner fluorometer; Potentiometric open-cell titration; Primary production/Photosynthesis; Radiation, photosynthetically active; Salinity; Scanning electron microscope (SEM); Single species; Temperature, water; Titration potentiometric
    Type: Dataset
    Format: text/tab-separated-values, 1396 data points
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  • 9
    Publication Date: 2024-05-27
    Keywords: 175-1078C; Acacia; Adenia; Afzelia; AGE; Alchornea; Alisma plantago-aquatica; Amaranthaceae/Chenopodiaceae; Anemia; Annonaceae; Anthoceros; Anthospermum; Avicennia; Balanites; Basella; Benguela Current, South Atlantic Ocean; Blighia-type; Botryococcus; Brachystegia; Bridelia; Burkea; Buxus-type madagascaria; Canthium spp.; Canthium subcordatum; Caryophyllaceae; Cassia-type; Celastraceae/Hippocrateaceae; Celtis; Cnestis-type; Coccinia; Colophospermum mopane; Combretaceae/Melastomataceae; Corymbium-type; Cotula-type; Counting, palynology; Crudia-type; Cussonia; Cyperaceae; Daisy-type; Daniellia-type; Dialium-type; Diospyros; DRILL; Drilling/drill rig; DSDP/ODP/IODP sample designation; Erica (Africa); Erythrina; Euphorbia; Fabaceae; Funtumia; Gazania-type; Geraniaceae; Geranium; Glomus; Hermannia; Hygrophila-type; Hymenocardia; Hypoestes type; Hyptis; Ilex cf.. mitis; Indigofera-type; Ipomoea-type; Isoberlinia-type; Joides Resolution; Justicia/Monechma; Kohautia; Lannea; Leg175; Liguliflorea-type; Liverwort; Maerua-type; Mallotus; Marker, added; Marker, found; Meliaceae; Monolete spore(s); Myrica; Myrsine africana; Nitraria; Ocean Drilling Program; ODP; Olea; Pelargonium; Pentzia-type; Pericopsis; Pheoceros; Phyllanthus; Poaceae; Podocarpus; Pollen, total; Pollen indeterminata; Polygonum senegalense-type; Protea; Pteris; Pyrite; Rhizophora; Rhus-type; Rothmannia; Sample code/label; Sapotaceae; Securinega; Sedimentation rate; Sherbournea; Spermacoce; Spindel; Spores, trilete; Stipularia africana; Stoebe-type; Tarchonanthus/Artemisia-type; Tephrosia; Tetrorchidium; Thymelaeaceae; Tribulus; Tubuliflorae-type; Typha spp.; Uapaca; Urticaceae; Varia; Vernonia-type; Zanthoxylum
    Type: Dataset
    Format: text/tab-separated-values, 12995 data points
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  • 10
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    Unknown
    PANGAEA
    Publication Date: 2024-05-27
    Keywords: Age model; Age model calibration; Angola Basin; Center for Marine Environmental Sciences; Charcoal; DEPTH, sediment/rock; GeoB1023-5; Gravity corer (Kiel type); M6/6; MARUM; Meteor (1986); SL
    Type: Dataset
    Format: text/tab-separated-values, 222 data points
    Location Call Number Expected Availability
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