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  • 1
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    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:  Supplement to: Bouimetarhan, Ilham; Groeneveld, Jeroen; Dupont, Lydie M; Zonneveld, Karin A F (2013): Low- to high- productivity pattern within Heinrich stadial 1: Inferrences from dinoflagellate cyst records off Senegal. Global and Planetary Change, https://doi.org/10.1016/j.gloplacha.2013.03.007
    Publication Date: 2024-05-27
    Description: In order to investigate a possible connection between tropical northeast (NE) Atlantic primary productivity, Atlantic meridional overturning circulation (AMOC), and drought in the Sahel region during Heinrich Stadial 1 (HS1), we used dinoflagellate cyst (dinocyst) assemblages, Mg/Ca based reconstructed temperatures, stable carbon isotopes (d13C) and geochemical parameters of a marine sediment core (GeoB 9508-5) from the continental slope offshore Senegal. Our results show a two-phase productivity pattern within HS1 that progressed from an interval of low marine productivity between ~ 19 and 16 kyr BP to a phase with an abrupt and large productivity increase from ~ 16 to 15 kyr BP. The second phase is characterized by distinct heavy planktonic d13C values and high concentrations of heterotrophic dinocysts in addition to a significant cooling signal based on reconstructions of past sea surface temperatures (SST). We conclude that productivity variations within HS1 can be attributed to a substantial shift of West African atmospheric processes. Taken together our results indicate a significant intensification of the North East (NE) trade winds over West Africa leading to more intense upwelling during the last millennium of HS1 between ~ 16 and 15 kyr BP, thus leaving a strong imprint on the dinocyst assemblages and sea surface conditions. Therefore, the two-phase productivity pattern indicates a complex hydrographic setting suggesting that HS1 cannot be regarded as uniform as previously thought.
    Keywords: Center for Marine Environmental Sciences; MARUM
    Type: Dataset
    Format: application/zip, 2 datasets
    Location Call Number Expected Availability
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  • 3
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    PANGAEA
    In:  Supplement to: Daniau, Anne-Laure; Bartlein, Patrick J; Harrison, S P; Prentice, Iain Colin; Brewer, Simon; Friedlingstein, Pierre; Harrison-Prentice, T I; Inoue, J; Izumi, K; Marlon, Jennifer R; Mooney, Scott D; Power, Mitchell J; Stevenson, J; Tinner, Willy; Andric, M; Atanassova, J; Behling, Hermann; Black, M; Blarquez, O; Brown, K J; Carcaillet, C; Colhoun, Eric A; Colombaroli, Daniele; Davis, Basil A S; D'Costa, D; Dodson, John; Dupont, Lydie M; Eshetu, Z; Gavin, D G; Genries, A; Haberle, Simon G; Hallett, D J; Hope, Geoffrey; Horn, S P; Kassa, T G; Katamura, F; Kennedy, L M; Kershaw, A Peter; Krivonogov, S; Long, C; Magri, Donatella; Marinova, E; McKenzie, G Merna; Moreno, P I; Moss, Patrick T; Neumann, F H; Norstrom, E; Paitre, C; Rius, D; Roberts, Neil; Robinson, G S; Sasaki, N; Scott, Louis; Takahara, H; Terwilliger, V; Thevenon, Florian; Turner, R; Valsecchi, V G; Vannière, Boris; Walsh, M; Williams, N; Zhang, Yancheng (2012): Predictability of biomass burning in response to climate changes. Global Biogeochemical Cycles, 26(4), https://doi.org/10.1029/2011GB004249
    Publication Date: 2024-05-27
    Description: We analyze sedimentary charcoal records to show that the changes in fire regime over the past 21,000 yrs are predictable from changes in regional climates. Analyses of paleo- fire data show that fire increases monotonically with changes in temperature and peaks at intermediate moisture levels, and that temperature is quantitatively the most important driver of changes in biomass burning over the past 21,000 yrs. Given that a similar relationship between climate drivers and fire emerges from analyses of the interannual variability in biomass burning shown by remote-sensing observations of month-by-month burnt area between 1996 and 2008, our results signal a serious cause for concern in the face of continuing global warming.
    Keywords: Center for Marine Environmental Sciences; MARUM
    Type: Dataset
    Format: application/zip, 2 datasets
    Location Call Number Expected Availability
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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: Bach, Lennart Thomas; Mackinder, Luke C M; Schulz, Kai Georg; Wheeler, Glen; Schroeder, Declan C; Brownlee, Colin; Riebesell, Ulf (2013): Dissecting the impact of CO2 and pH on the mechanisms of photosynthesis and calcification in the coccolithophore Emiliania huxleyi. New Phytologist, 199(1), 121-134, https://doi.org/10.1111/nph.12225
    Publication Date: 2024-05-27
    Description: Coccolithophores are important calcifying phytoplankton predicted to be impacted by changes in ocean carbonate chemistry caused by the absorption of anthropogenic CO2. However, it is difficult to disentangle the effects of the simultaneously changing carbonate system parameters (CO2, bicarbonate, carbonate and protons) on the physiological responses to elevated CO2. Here, we adopted a multifactorial approach at constant pH or CO2 whilst varying dissolved inorganic carbon (DIC) to determine physiological and transcriptional responses to individual carbonate system parameters. We show that Emiliania huxleyi is sensitive to low CO2 (growth and photosynthesis) and low bicarbonate (calcification) as well as low pH beyond a limited tolerance range, but is much less sensitive to elevated CO2 and bicarbonate. Multiple up-regulated genes at low DIC bear the hallmarks of a carbon-concentrating mechanism (CCM) that is responsive to CO2 and bicarbonate but not to pH. Emiliania huxleyi appears to have evolved mechanisms to respond to limiting rather than elevated CO2. Calcification does not function as a CCM, but is inhibited at low DIC to allow the redistribution of DIC from calcification to photosynthesis. The presented data provides a significant step in understanding how E. huxleyi will respond to changing carbonate chemistry at a cellular level
    Keywords: Alkalinity, total; alpha carbonic anhydrase 1; alpha carbonic anhydrase 1, standard error; alpha carbonic anhydrase 2; alpha carbonic anhydrase 2, standard error; Anion exchanger like 1; Anion exchanger like 1, standard error; Aquaporin 2; Aquaporin 2, standard error; Aragonite saturation state; beta carbonic anhydrase; beta carbonic anhydrase, standard error; Bicarbonate ion; BIOACID; Biological Impacts of Ocean Acidification; Ca2+/H+ exchanger 3; Ca2+/H+ exchanger 3, standard error; Calcification/Dissolution; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, particulate, production per cell; Carbon, organic, particulate, production per cell; Carbon/Nitrogen ratio; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Chlorophyll a; Chromista; Containers and aquaria (20-1000 L or 〈 1 m**2); delta carbonic anhydrase; delta carbonic anhydrase, standard error; Difference; Emiliania huxleyi; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); gamma carbonic anhydrase, mean; gamma carbonic anhydrase, standard error; Glutamic acid, proline, alanine rich protein; Glutamic acid, proline, alanine rich protein, standard error; Growth/Morphology; Growth rate; Haptophyta; Irradiance; Laboratory experiment; Laboratory strains; Light:Dark cycle; Low CO2 induced gene; Low CO2 induced gene, standard error; Na+/H+ exchanger 2; Na+/H+ exchanger 2, standard error; 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; Plasma membran type H+ pump; Plasma membran type H+ pump, standard error; Primary production/Photosynthesis; RubisCO; RubisCO, standard error; Salinity; Single species; Species; Temperature, water; Treatment; Vacuolar-type H+ pump; Vacuolar-type H+ pump, standard error; Voltage-gated H+ channel; Voltage-gated H+ channel, standard error
    Type: Dataset
    Format: text/tab-separated-values, 1165 data points
    Location Call Number Expected Availability
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  • 8
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    PANGAEA
    In:  Supplement to: Spungin, D; Berman-Frank, I; Levitan, Orly (2014): Trichodesmium's strategies to alleviate phosphorus limitation in the future acidified oceans. Environmental Microbiology, 16(6), 1935-1947, https://doi.org/10.1111/1462-2920.12424
    Publication Date: 2024-05-27
    Description: Global warming may exacerbate inorganic nutrient limitation, including phosphorus (P), in the surface-waters of tropical oceans that are home to extensive blooms of the marine diazotrophic cyanobacterium, Trichodesmium. We examined the combined effects of P limitation and pCO2, forecast under ocean acidification scenarios, on Trichodesmium erythraeum IMS101 cultures. We measured nitrogen acquisition, glutamine synthetase activity, C uptake rates, intracellular Adenosine Triphosphate (ATP) concentration and the pool sizes of related key proteins. Here, we present data supporting the idea that cellular energy re-allocation enables the higher growth and N2 fixation rates detected in Trichodesmium cultured under high pCO2. This is reflected in altered protein abundance and metabolic pools. Also modified are particulate organic carbon and nitrogen production rates, enzymatic activities, and cellular ATP concentrations. We suggest that adjusting these cellular pathways to changing environmental conditions enables Trichodesmium to compensate for low P availability and to thrive in acidified oceans. Moreover, elevated pCO2 could provide Trichodesmium with a competitive dominance that would extend its niche, particularly in P-limited regions of the tropical and subtropical oceans.
    Keywords: Adenosine 5-Triphosphate, per cell; Adenosine 5-Triphosphate, standard deviation; Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Bacteria; 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, production per cell; Carbon/Nitrogen ratio; Carbon/Nitrogen ratio, standard deviation; Carbon/Phosphorus ratio; Carbon/Phosphorus ratio, standard deviation; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, standard deviation; Carbon uptake rate, standard deviation; Carbon uptake rate per cell; CF1 subunit of ATP synthase protein; CF1 subunit of ATP synthase protein, standard deviation; Chlorophyll a, standard deviation; Chlorophyll a per cell; Cyanobacteria; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); GlnA subunit of Gln synthetase; GlnA subunit of Gln synthetase, standard deviation; Glutamine synthetase biosynthetic activity, standard deviation; Glutamine synthetase biosynthetic activity per cell; Glutamine synthetase transferase/biosynthetic activity ratio; Glutamine synthetase transferase/biosynthetic activity ratio, standard deviation; Growth rate; Growth rate, standard deviation; Incubation duration; Iron protein of nitrogenase; Iron protein of nitrogenase, standard deviation; Laboratory experiment; Laboratory strains; Length; Length, standard deviation; Macro-nutrients; Nitrogen/Phosphorus ratio; Nitrogen/Phosphorus ratio, standard deviation; Not applicable; OA-ICC; Ocean Acidification International Coordination Centre; Other metabolic rates; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Particulate organic carbon, per cell; Particulate organic carbon, production, standard deviation; Particulate organic carbon content per cell, standard deviation; Particulate organic nitrogen, standard deviation; Particulate organic nitrogen per cell; Particulate organic nitrogen production, standard deviation; Particulate organic phosphorus, standard deviation; Particulate organic phosphorus per cell; Pelagos; pH; pH, standard deviation; Phosphate; Photosynthetic protein, PsbA, standard deviation; Photosynthetic protein, PsbC; Photosynthetic protein, PsbC, standard deviation; Photosynthetic protein PsbA; Photosynthetic protein Rubisco; Photosynthetic protein Rubisco, standard deviation; Phytoplankton; Primary production/Photosynthesis; Production of particulate organic nitrogen; Salinity; Single species; Species; Temperature, water; Trichodesmium erythraeum
    Type: Dataset
    Format: text/tab-separated-values, 1003 data points
    Location Call Number Expected Availability
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  • 9
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    PANGAEA
    In:  Supplement to: Müller, Marius N; Lebrato, Mario; Riebesell, Ulf; Barcelos e Ramos, Joana; Schulz, Kai Georg; Blanco-Ameijeiras, S; Sett, Scarlett; Eisenhauer, Anton; Stoll, Heather M (2014): Influence of temperature and CO2 on the strontium and magnesium composition of coccolithophore calcite. Biogeosciences, 11(4), 1065-1075, https://doi.org/10.5194/bg-11-1065-2014
    Publication Date: 2024-05-27
    Description: Marine calcareous sediments provide a fundamental basis for palaeoceanographic studies aiming to reconstruct past oceanic conditions and understand key biogeochemical element cycles. Calcifying unicellular phytoplankton (coccolithophores) are a major contributor to both carbon and calcium cycling by photosynthesis and the production of calcite (coccoliths) in the euphotic zone, and the subsequent long-term deposition and burial into marine sediments. Here we present data from controlled laboratory experiments on four coccolithophore species and elucidate the relation between the divalent cation (Sr, Mg and Ca) partitioning in coccoliths and cellular physiology (growth, calcification and photosynthesis). Coccolithophores were cultured under different seawater temperature and carbonate chemistry conditions. The partition coefficient of strontium (DSr) was positively correlated with both carbon dioxide (pCO2) and temperature but displayed no coherent relation to particulate organic and inorganic carbon production rates. Furthermore, DSr correlated positively with cellular growth rates when driven by temperature but no correlation was present when changes in growth rates were pCO2-induced. Our results demonstrate the complex interaction between environmental forcing and physiological control on the strontium partitioning in coccolithophore calcite and challenge interpretations of the coccolith Sr / Ca ratio from high-pCO2 environments (e.g. Palaeocene-Eocene thermal maximum). The partition coefficient of magnesium (DMg) displayed species-specific differences and elevated values under nutrient limitation. No conclusive correlation between coccolith DMg and temperature was observed but pCO2 induced a rising trend in coccolith DMg. Interestingly, the best correlation was found between coccolith DMg and chlorophyll a production, suggesting that chlorophyll a and calcite associated Mg originate from the same intracellular pool. These and previous findings indicate that Mg is transported into the cell and to the site of calcification via different pathways than Ca and Sr. Consequently, the coccolith Mg / Ca ratio should be decoupled from the seawater Mg / Ca ratio. This study gives an extended insight into the driving factors influencing the coccolith Mg / Ca ratio and should be considered for future palaeoproxy calibrations.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Bicarbonate ion; Bicarbonate ion, standard deviation; Biomass/Abundance/Elemental composition; Bottles or small containers/Aquaria (〈20 L); Calcidiscus quadriperforatus; Calcite saturation state; Calcite saturation state, standard deviation; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbon, inorganic, particulate, production per cell; Carbon, organic, particulate, production per cell; Carbon, organic, particulate/Nitrogen, particulate ratio; Carbon, organic, particulate/Nitrogen, particulate ratio, standard deviation; Carbonate ion; Carbonate ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, standard deviation; Chlorophyll a, production, standard deviation; Chlorophyll a production per cell; Chromista; Coccolithus braarudii; Coulometric titration; Emiliania huxleyi; Experiment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Gephyrocapsa oceanica; Growth rate; Growth rate, standard deviation; Haptophyta; Iron/Calcium ratio; Irradiance; Laboratory experiment; Laboratory strains; Light:Dark cycle; Magnesium/Calcium ratio; Magnesium/Calcium ratio, standard deviation; Magnesium distribution coefficient; Nitrogen, total, particulate, production per cell; Nitrogen, total, particulate production, 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 inorganic carbon, production, standard deviation; Particulate inorganic carbon/particulate organic carbon ratio; Particulate inorganic carbon/particulate organic carbon ratio, standard deviation; Particulate organic carbon, production, standard deviation; Pelagos; pH; pH, standard deviation; Phosphorus/Calcium ratio; Phytoplankton; Potentiometric titration; Salinity; Single species; Species; Strontium, partition coefficient; Strontium/Calcium ratio; Strontium/Calcium ratio, standard deviation; Temperature, water
    Type: Dataset
    Format: text/tab-separated-values, 2247 data points
    Location Call Number Expected Availability
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    In:  Supplement to: Sett, Scarlett; Bach, Lennart Thomas; Schulz, Kai Georg; Koch-Klavsen, Signe; Lebrato, Mario; Riebesell, Ulf (2014): Temperature Modulates Coccolithophorid Sensitivity of Growth, Photosynthesis and Calcification to Increasing Seawater pCO2. PLoS ONE, 9(2), e88308, https://doi.org/10.1371/journal.pone.0088308
    Publication Date: 2024-05-27
    Description: Increasing atmospheric CO2 concentrations are expected to impact pelagic ecosystem functioning in the near future by driving ocean warming and acidification. While numerous studies have investigated impacts of rising temperature and seawater acidification on planktonic organisms separately, little is presently known on their combined effects. To test for possible synergistic effects we exposed two coccolithophore species, Emiliania huxleyi and Gephyrocapsa oceanica, to a CO2 gradient ranging from ~0.5-250 µmol/kg (i.e. ~20-6000 µatm pCO2) at three different temperatures (i.e. 10, 15, 20°C for E. huxleyi and 15, 20, 25°C for G. oceanica). Both species showed CO2-dependent optimum-curve responses for growth, photosynthesis and calcification rates at all temperatures. Increased temperature generally enhanced growth and production rates and modified sensitivities of metabolic processes to increasing CO2. CO2 optimum concentrations for growth, calcification, and organic carbon fixation rates were only marginally influenced from low to intermediate temperatures. However, there was a clear optimum shift towards higher CO2 concentrations from intermediate to high temperatures in both species. Our results demonstrate that the CO2 concentration where optimum growth, calcification and carbon fixation rates occur is modulated by temperature. Thus, the response of a coccolithophore strain to ocean acidification at a given temperature can be negative, neutral or positive depending on that strain's temperature optimum. This emphasizes that the cellular responses of coccolithophores to ocean acidification can only be judged accurately when interpreted in the proper eco-physiological context of a given strain or species. Addressing the synergistic effects of changing carbonate chemistry and temperature is an essential step when assessing the success of coccolithophores in the future ocean.
    Keywords: Alkalinity, total; Aragonite saturation state; Bicarbonate ion; 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; Chromista; Emiliania huxleyi; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Gephyrocapsa oceanica; Growth/Morphology; Growth rate; Haptophyta; Laboratory experiment; Laboratory strains; 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; Phytoplankton; Potentiometric titration; Primary production/Photosynthesis; Salinity; Single species; Species; Temperature; Temperature, water
    Type: Dataset
    Format: text/tab-separated-values, 1958 data points
    Location Call Number Expected Availability
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