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  • 1
    Publication Date: 2022-05-26
    Description: Author Posting. © The Author(s), 2017. This is the author's version of the work. It is posted here under a nonexclusive, irrevocable, paid-up, worldwide license granted to WHOI. It is made available for personal use, not for redistribution. The definitive version was published in Science 357 (2017): eaao0067, doi:10.1126/science.aao0067.
    Description: Hong et al. (Reports, 5 May 2017, p. 527) suggested that previous studies of the biogeochemically significant marine cyanobacterium Trichodesmium showing increased growth and nitrogen fixation at projected future high CO2 levels suffered from ammonia or copper toxicity. They reported that these rates instead decrease at high CO2 when contamination is alleviated. We present and discuss results of multiple published studies refuting this toxicity hypothesis.
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
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  • 2
    Publication Date: 2024-04-03
    Description: In addition to ocean acidification, a significant recent warming trend in Chinese coastal waters has received much attention. However, studies of the combined effects of warming and acidification on natural coastal phytoplankton assemblages here are scarce. We conducted a continuous incubation experiment with a natural spring phytoplankton assemblage collected from the Bohai Sea near Tianjin. Experimental treatments used a full factorial combination of temperature (7 and 11°C) and pCO2 (400 and 800 ppm) treatments. Results suggest that changes in pCO2 and temperature had both individual and interactive effects on phytoplankton species composition and elemental stoichiometry. Warming mainly favored the accumulation of picoplankton and dinoflagellate biomass. Increased pCO2 significantly increased particulate organic carbon to particulate organic phosphorus (C:P) and particulate organic carbon to biogenic silica (C:BSi) ratios, and decreased total diatom abundance; in the meanwhile, higher pCO2 significantly increased the ratio of centric to pennate diatom abundance. Warming and increased pCO2 both greatly decreased the proportion of diatoms to dinoflagellates. The highest chlorophyll a biomass was observed in the high pCO2, high temperature phytoplankton assemblage, which also had the slowest sinking rate of all treatments. Overall, there were significant interactive effects of increased pCO2 and warming on dinoflagellate abundance, pennate diatom abundance, diatom vs. dinoflagellates ratio and the centric vs. pennate ratio. These findings suggest that future ocean acidification and warming trends may individually and cumulatively affect coastal biogeochemistry and carbon fluxes through shifts in phytoplankton species composition and sinking rates.
    Keywords: Abundance; Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Aragonite saturation state, standard deviation; Bicarbonate ion; Bicarbonate ion, standard deviation; Biogenic silica; Biomass/Abundance/Elemental composition; Bohai_Bay; 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); Calculated using seacarb after Orr et al. (2018); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbon, organic, particulate; Carbon/Nitrogen ratio; Carbon/Phosphorus ratio; Carbon/Silicon ratio; Carbonate ion; Carbonate ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, standard deviation; Coast and continental shelf; Community composition and diversity; Entire community; EXP; Experiment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Fugacity of carbon dioxide in seawater, standard deviation; Laboratory experiment; Nitrogen, organic, particulate; Nitrogen/Phosphorus ratio; North Pacific; OA-ICC; Ocean Acidification International Coordination Centre; Other studied parameter or process; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; pH, standard deviation; Phosphorus, organic, particulate; Potentiometric; Ratio; Salinity; Sinking velocity; Temperate; Temperature; Temperature, water; Treatment; Type
    Type: Dataset
    Format: text/tab-separated-values, 312 data points
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  • 3
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    PANGAEA
    In:  Supplement to: Liu, Xin; Li, Yan; Wu, YaPing; Huang, Bangqin; Dai, Minhan; Fu, Feixue; Hutchins, David A; Gao, Kunshan (2017): Effects of elevated CO2 on phytoplankton during a mesocosm experiment in the southern eutrophicated coastal water of China. Scientific Reports, 7(1), https://doi.org/10.1038/s41598-017-07195-8
    Publication Date: 2024-04-03
    Description: There is a growing consensus that the ongoing increase in atmospheric CO2 level will lead to a variety of effects on marine phytoplankton and ecosystems. However, the effects of CO2 enrichment on eutrophic coastal waters are still unclear, as are the complex mechanisms coupled to the development of eutrophication. Here, we report the first mesocosm CO2 perturbation study in a eutrophic subtropical bay during summer by investigating the effect of rising CO2 on a model artificial community consisting of well-characterized cultured diatoms (Phaeodactylum tricornutum and Thalassiosira weissflogii) and prymnesiophytes (Emiliania huxleyi and Gephyrocapsa oceanica). These species were inoculated into triplicate 4 m**3 enclosures with equivalent chlorophyll a (Chl-a) under present and higher partial pressures of atmospheric CO2 (pCO2 = 400 and 1000 ppmv). Diatom bloom events were observed in all enclosures, with enhanced organic carbon production and Chl-a concentrations under high CO2 treatments. Relative to the low CO2 treatments, the consumption of the dissolved inorganic nitrogen and uptake ratios of N/P and N/Si increased significantly during the bloom. These observed responses suggest more extensive and complex effects of higher CO2 concentrations on phytoplankton communities in coastal eutrophic environments.
    Keywords: 19-Hexanoyloxyfucoxanthin; 19-Hexanoyloxyfucoxanthin, standard deviation; 19-Hexanoyloxyfucoxanthin/chlorophyll a; 19-Hexanoyloxyfucoxanthin/chlorophyll a, standard deviation; Alkalinity, total; Alkalinity, total, standard deviation; Ammonium; Ammonium, standard deviation; Aragonite saturation state; Bicarbonate ion; Biomass/Abundance/Elemental composition; Calcification/Dissolution; Calcification rate of calcium carbonate; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Chlorophyll a; Chlorophyll a, standard deviation; Coast and continental shelf; Entire community; EXP; Experiment; Field experiment; Fucoxanthin; Fucoxanthin, standard deviation; Fucoxanthin/chlorophyll a ratio; Fucoxanthin/chlorophyll a ratio, standard devitation; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Identification; Mesocosm or benthocosm; Nitrate and Nitrite; Nitrate and Nitrite, standard deviation; Nitrogen, inorganic, dissolved; Nitrogen, inorganic, dissolved, standard deviation; Nitrogen/Phosphorus ratio; Nitrogen/Phosphorus ratio, standard deviation; Nitrogen/Silicon ratio; Nitrogen/Silicon ratio, standard deviation; North Pacific; 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/particulate organic carbon ratio; Particulate organic carbon production; Pelagos; pH; pH, standard deviation; Phosphate; Phosphate, standard deviation; Primary production/Photosynthesis; Production of Carbon, organic, dissolved; Ratio; Ratio, standard deviation; Salinity; Salinity, standard deviation; Silicate; Temperate; Temperature, water; Temperature, water, standard deviation; Time in days; Treatment; Type; Wuyuan_Bay
    Type: Dataset
    Format: text/tab-separated-values, 1150 data points
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  • 4
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    PANGAEA
    In:  Supplement to: Tatters, Avery O; Fu, Feixue; Hutchins, David A (2012): High CO2 and Silicate Limitation Synergistically Increase the Toxicity of Pseudo-nitzschia fraudulenta. PLoS ONE, 7(2), e32116, https://doi.org/10.1371/journal.pone.0032116.g004
    Publication Date: 2024-04-03
    Description: Anthropogenic CO2 is progressively acidifying the ocean, but the responses of harmful algal bloom species that produce toxins that can bioaccumulate remain virtually unknown. The neurotoxin domoic acid is produced by the globally-distributed diatom genus Pseudo-nitzschia. This toxin is responsible for amnesic shellfish poisoning, which can result in illness or death in humans and regularly causes mass mortalities of marine mammals and birds. Domoic acid production by Pseudo-nitzschia cells is known to be regulated by nutrient availability, but potential interactions with increasing seawater CO2 concentrations are poorly understood. Here we present experiments measuring domoic acid production by acclimatized cultures of Pseudo-nitzschia fraudulenta that demonstrate a strong synergism between projected future CO2 levels (765 ppm) and silicate-limited growth, which greatly increases cellular toxicity relative to growth under modern atmospheric (360 ppm) or pre-industrial (200 ppm) CO2 conditions. Cellular Si:C ratios decrease with increasing CO2, in a trend opposite to that seen for domoic acid production. The coastal California upwelling system where this species was isolated currently exhibits rapidly increasing levels of anthropogenic acidification, as well as widespread episodic silicate limitation of diatom growth. Our results suggest that the current ecosystem and human health impacts of toxic Pseudo-nitzschia blooms could be greatly exacerbated by future ocean acidification and 'carbon fertilization' of the coastal ocean.
    Keywords: Alkalinity, total; Aragonite saturation state; Bicarbonate ion; Biogenic silica; Biomass/Abundance/Elemental composition; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, organic, particulate; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Cell density; Chromista; Coast and continental shelf; Coulometric titration; Domoic acid per cell; Domoic acid production per cell; EXP; Experiment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; High Performance Liquid Chromatography (HPLC); Immunology/Self-protection; Laboratory experiment; Macro-nutrients; Nitrogen, organic, particulate; North Pacific; OA-ICC; Ocean Acidification International Coordination Centre; Ochrophyta; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; Phosphorus, organic, particulate; Phytoplankton; Potentiometric; Pseudo-nitzschia fraudulenta; Replicate; Salinity; Single species; Species; Temperate; Temperature, water; Treatment; Ventura
    Type: Dataset
    Format: text/tab-separated-values, 439 data points
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  • 5
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    PANGAEA
    In:  Supplement to: Tatters, Avery O; Schnetzer, Astrid; Fu, Feixue; Lie, Alle Y A; Caron, David A; Hutchins, David A (2013): Short- versus long-term responses to changing CO2 in a coastal dinoflagellate bloom: implications for interspecific competitive interactions and community structure. Evolution, 67(7), 1879-1891, https://doi.org/10.1111/evo.12029
    Publication Date: 2024-04-03
    Description: Increasing pCO2 (partial pressure of CO2 ) in an "acidified" ocean will affect phytoplankton community structure, but manipulation experiments with assemblages briefly acclimated to simulated future conditions may not accurately predict the long-term evolutionary shifts that could affect inter-specific competitive success. We assessed community structure changes in a natural mixed dinoflagellate bloom incubated at three pCO2 levels (230, 433, and 765 ppm) in a short-term experiment (2 weeks). The four dominant species were then isolated from each treatment into clonal cultures, and maintained at all three pCO2 levels for approximately 1 year. Periodically (4, 8, and 12 months), these pCO2 -conditioned clones were recombined into artificial communities, and allowed to compete at their conditioning pCO2 level or at higher and lower levels. The dominant species in these artificial communities of CO2 -conditioned clones differed from those in the original short-term experiment, but individual species relative abundance trends across pCO2 treatments were often similar. Specific growth rates showed no strong evidence for fitness increases attributable to conditioning pCO2 level. Although pCO2 significantly structured our experimental communities, conditioning time and biotic interactions like mixotrophy also had major roles in determining competitive outcomes. New methods of carrying out extended mixed species experiments are needed to accurately predict future long-term phytoplankton community responses to changing pCO2 .
    Keywords: Alexandrium sp.; 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; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Cell density; Chromista; Coast and continental shelf; Coulometric titration; Coulometry; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Gonyaulax sp.; Growth/Morphology; Growth rate; Identification; Incubation duration; Laboratory experiment; Lingulodinium polyedrum; Myzozoa; North Pacific; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; pH meter; Phytoplankton; Potentiometric; Prorocentrum micans; Replicate; Salinity; Species; Species interaction; Temperate; Temperature, water; Treatment; Tropical
    Type: Dataset
    Format: text/tab-separated-values, 5616 data points
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  • 6
    Publication Date: 2024-04-03
    Description: We describe interactive effects of total phosphorus (total P = 0.1-4.0 µmol/L; added as H2NaPO4), irradiance (40 and 150 µmol quanta/m**2/s), and the partial pressure of carbon dioxide (P-CO2; 19 and 81 Pa, i.e., 190 and 800 ppm) on growth and CO2- and dinitrogen (N-2)-fixation rates of the unicellular N-2-fixing cyanobacterium Crocosphaera watsonii (WH0003) isolated from the Pacific Ocean near Hawaii. In semicontinuous cultures of C. watsonii, elevated P-CO2 positively affected growth and CO2- and N-2-fixation rates under high light. Under low light, elevated P-CO2 positively affected growth rates at all concentrations of P, but CO2- and N-2-fixation rates were affected by elevated P-CO2 only when P was low. In both high-light and low-light cultures, the total P requirements for growth and CO2- and N-2-fixation declined as P-CO2 increased. The minimum concentration (C-min) of total P and half-saturation constant (K-1/2) for growth and CO2- and N-2-fixation rates with respect to total P were reduced by 0.05 µmol/L as a function of elevated P-CO2. We speculate that low P requirements under high P-CO2 resulted from a lower energy demand associated with carbon-concentrating mechanisms in comparison with low-P-CO2 cultures. There was also a 0.10 µmol/L increase in C-min and K-1/2 for growth and N-2 fixation with respect to total P as a function of increasing light regardless of P-CO2 concentration. We speculate that cellular P concentrations are responsible for this shift through biodilution of cellular P and possibly cellular P uptake systems as a function of increasing light. Changing concentrations of P, CO2, and light have both positive and negative interactive effects on growth and CO2-, and N-2-fixation rates of unicellular oxygenic diazotrophs like C. watsonii.
    Keywords: Alkalinity, total; 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; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Carbon fixation rate, per cellular phosphorus; Cellular phosphorus, per cell volume; Coulometric titration; Crocosphaera watsonii; Cyanobacteria; Diameter; Diameter, standard error; Figure; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; Irradiance; Laboratory experiment; Laboratory strains; Light; log-phosphorus, total; Macro-nutrients; Nitrogen fixation rate, gross, per cellular phosphorus; Nitrogen fixation rate, per cell; North Pacific; OA-ICC; Ocean Acidification International Coordination Centre; Other metabolic rates; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; Phosphorus, total; Phosphorus, total, per cell; Phosphorus uptake rate, per cell; Phosphorus uptake rate/growth rate ratio; Photosynthetic carbon fixation per cell, maximum velocity; Photosynthetic carbon fixation rate per cell; Phytoplankton; Potentiometric; Primary production/Photosynthesis; Salinity; Single species; Species; Table; Temperature, water; Time point, descriptive
    Type: Dataset
    Format: text/tab-separated-values, 6388 data points
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  • 7
    Publication Date: 2024-04-03
    Description: Phytoplankton growth can be limited by numerous inorganic nutrients and organic growth factors. Using the subarctic diatom Attheya sp. in culture studies, we examined how the availability of vitamin B(12) and carbon dioxide partial pressure (pCO(2)) influences growth rate, primary productivity, cellular iron (Fe), cobalt (Co), zinc (Zn) and cadmium (Cd) quotas, and the net use efficiencies (NUEs) of these bioactive trace metals (mol C fixed per mol cellular trace metal per day). Under B(12)-replete conditions, cells grown at high pCO(2) had lower Fe, Zn and Cd quotas, and used those trace metals more efficiently in comparison with cells grown at low pCO(2). At high pCO(2), B(12)-limited cells had ~50% lower specific growth and carbon fixation rates, and used Fe ~15-fold less efficiently, and Zn and Cd ~3-fold less efficiently, in comparison with B(12)-replete cells. The observed higher Fe, Zn and Cd NUE under high pCO(2)/B(12)-replete conditions are consistent with predicted downregulation of carbon-concentrating mechanisms. Co quotas of B(12)-replete cells were 5- to 14-fold higher in comparison with B(12)-limited cells, suggesting that 〉80% of cellular Co of B(12)-limited cells was likely from B(12). Our results demonstrate that CO(2) and vitamin B(12) interactively influence growth, carbon fixation, trace metal requirements and trace metal NUE of this diatom. This suggests the need to consider complex feedback interactions between multiple environmental factors for this biogeochemically critical group of phytoplankton in the last glacial maximum as well as the current and future changing ocean.
    Keywords: Alkalinity, total; Aragonite saturation state; Attheya sp.; Bicarbonate ion; Biomass/Abundance/Elemental composition; Bottles or small containers/Aquaria (〈20 L); Cadmium/Phosphorus ratio; Cadmium/Phosphorus ratio, standard deviation; Calcite saturation state; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbon/Phosphorus ratio; Carbon/Phosphorus ratio, standard deviation; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Chromista; Cobalt/Phosphorus ratio; Cobalt/Phosphorus ratio, standard deviation; Coulometric titration; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; Growth rate, standard deviation; Iron/Phosphorus ratio; Iron/Phosphorus ratio, standard deviation; Laboratory experiment; Laboratory strains; Micro-nutrients; Net use efficiency, Cadmium; Net use efficiency, Cadmium, standard deviation; Net use efficiency, Cobalt; Net use efficiency, Cobalt, standard deviation; Net use efficiency, Iron; Net use efficiency, Iron, standard deviation; Net use efficiency, Zinc; Net use efficiency, Zinc, standard deviation; Nitrogen/Phosphorus ratio; Nitrogen/Phosphorus ratio, standard deviation; North Pacific; OA-ICC; Ocean Acidification International Coordination Centre; Ochrophyta; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; pH, standard deviation; Phytoplankton; Potentiometric; Primary production; Primary production/Photosynthesis; Primary production of carbon, standard deviation; Salinity; Single species; Species; Temperature, water; Treatment; Zinc/Phosphorus ratio; Zinc/Phosphorus ratio, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 270 data points
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  • 8
    Publication Date: 2024-04-03
    Description: We examined the combined effects of light and pCO2 on growth, CO2-fixation and N2-fixation rates by strains of the unicellular marine N2-fixing cyanobacterium Crocosphaera watsonii with small (WH0401) and large (WH0402) cells that were isolated from the western tropical Atlantic Ocean. In low-pCO2-acclimated cultures (190 ppm) of WH0401, growth, CO2-fixation and N2-fixation rates were significantly lower than those in cultures acclimated to higher (present-day 385 ppm, or future 750 ppm) pCO2 treatments. Growth rates were not significantly different, however, in low-pCO2-acclimated cultures of WH0402 in comparison with higher pCO2 treatments. Unlike previous reports for C. watsonii (strain WH8501), N2-fixation rates did not increase further in cultures of WH0401 or WH0402 when acclimated to 750 ppm relative to those maintained at present-day pCO2. Both light and pCO2 had a significant negative effect on gross : net N2-fixation rates in WH0402 and trends were similar in WH0401, implying that retention of fixed N was enhanced under elevated light and pCO2. These data, along with previously reported results, suggest that C. watsonii may have wide-ranging, strain-specific responses to changing light and pCO2, emphasizing the need for examining the effects of global change on a range of isolates within this biogeochemically important genus. In general, however, our data suggest that cellular N retention and CO2-fixation rates of C. watsonii may be positively affected by elevated light and pCO2 within the next 100 years, potentially increasing trophic transfer efficiency of C and N and thereby facilitating uptake of atmospheric carbon by the marine biota.
    Keywords: 15N2-tracer method; Alkalinity, total; 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; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Carbon fixation rate, photosynthetic; Coulometric titration; Crocosphaera watsonii; Cyanobacteria; Diameter; Diameter, standard error; Figure; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; Growth rate, standard deviation; Irradiance; Laboratory experiment; Laboratory strains; Light; Nitrogen, particulate, accumulation, per cell; Nitrogen, particulate, accumulation, standard deviation; Nitrogen fixation rate; Nitrogen fixation rate, gross/nitrogen fixation rate, netto ratio; Nitrogen fixation rate, gross/nitrogen fixation rate, netto ratio, standard deviation; Nitrogen fixation rate, gross/particulate nitrogen, netto, accumulation rate ratio; Nitrogen fixation rate, gross/particulate nitrogen, netto, accumulation rate ratio, standard deviation; Nitrogen fixation rate, per cell; Nitrogen fixation rate, standard deviation; North Pacific; OA-ICC; Ocean Acidification International Coordination Centre; Other metabolic rates; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; pH, standard deviation; Photosynthetic carbon fixation rate, standard deviation; Photosynthetic carbon fixation rate per cell; Phytoplankton; Potentiometric; Primary production/Photosynthesis; Salinity; Single species; Species; Strain; Temperature, water
    Type: Dataset
    Format: text/tab-separated-values, 1043 data points
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  • 9
    Publication Date: 2024-04-03
    Description: Ocean acidification and greenhouse warming will interactively influence competitive success of key phytoplankton groups such as diatoms, but how long-term responses to global change will affect community structure is unknown. We incubated a mixed natural diatom community from coastal New Zealand waters in a short-term (two-week) incubation experiment using a factorial matrix of warming and/or elevated pCO2 and measured effects on community structure. We then isolated the dominant diatoms in clonal cultures and conditioned them for 1 year under the same temperature and pCO2 conditions from which they were isolated, in order to allow for extended selection or acclimation by these abiotic environmental change factors in the absence of interspecific interactions. These conditioned isolates were then recombined into 'artificial' communities modelled after the original natural assemblage and allowed to compete under conditions identical to those in the short-term natural community experiment. In general, the resulting structure of both the unconditioned natural community and conditioned 'artificial' community experiments was similar, despite differences such as the loss of two species in the latter. pCO2 and temperature had both individual and interactive effects on community structure, but temperature was more influential, as warming significantly reduced species richness. In this case, our short-term manipulative experiment with a mixed natural assemblage spanning weeks served as a reasonable proxy to predict the effects of global change forcing on diatom community structure after the component species were conditioned in isolation over an extended timescale. Future studies will be required to assess whether or not this is also the case for other types of algal communities from other marine regimes.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Aragonite saturation state, standard deviation; 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); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbonate ion; Carbonate ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Cell density; Chaetoceros criophilus; Coast and continental shelf; Community composition and diversity; Coscinodiscus sp.; Coulometric titration; Cylindrotheca fusiformis; Entire community; Experiment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; Growth rate, standard deviation; Incubation duration; Laboratory experiment; Navicula sp.; 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; Pseudonitzschia delicatissima; Salinity; Sample ID; South Pacific; Species; Spectrophotometric; Temperate; Temperature; Temperature, water; Thalassiosira sp.; Treatment
    Type: Dataset
    Format: text/tab-separated-values, 10188 data points
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  • 10
    Publication Date: 2024-05-02
    Description: To gain a better understanding of what drives Pseudo-nitzschia australis growth and toxicity during upwelling and marine heatwave events, multiple-driver scenario or 'cluster' experiments were conducted using temperature, pCO2, and nutrient levels reflecting conditions during upwelling (13 ◦C, 900 ppm pCO2, replete nutrients) and two intensities of marine heatwaves (19 ◦C or 20.5 ◦C, 250 ppm pCO2, reduced macronutrients). We also conducted single-driver experiments to gain a mechanistic understanding of which drivers most impact P. australis growth and toxicity.
    Keywords: Alkalinity, total; Aragonite saturation state; Bacillariophyta; 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; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Chromista; Domoic acid per cell; Domoic acid production per particulate organic carbon; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; Immunology/Self-protection; Laboratory experiment; Laboratory strains; Macro-nutrients; Net primary production of carbon per particulate organic carbon; Net primary production of carbon per particulate organic nitrogen; Not applicable; OA-ICC; Ocean Acidification International Coordination Centre; Other studied parameter or process; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Particulate domoic acid per particulate organic carbon; Pelagos; pH; Phytoplankton; Primary production/Photosynthesis; Pseudo-nitzschia australis; Replicate; Salinity; Single species; Species, unique identification; Species, unique identification (Semantic URI); Species, unique identification (URI); Temperature; Temperature, water; Treatment; Type of study
    Type: Dataset
    Format: text/tab-separated-values, 867 data points
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