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  • Electronic books.  (2)
  • Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Bicarbonate ion; Bicarbonate ion, standard deviation; Bottles or small containers/Aquaria (〈20 L); Calcification/Dissolution; Calcification rate, standard deviation; Calcification rate/Photosynthesis rate, ratio; Calcification rate/Photosynthesis rate, ratio, standard deviation; Calcification rate of carbon per cell; 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 ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, standard deviation; Carotenoids, standard deviation; Carotenoids per cell; Cell, diameter; Cell, diameter, standard deviation; Chlorophyll a, standard deviation; Chlorophyll a per cell; Chlorophyll c, standard deviation; Chlorophyll c per cell; Chromista; Effective quantum yield; Effective quantum yield, standard deviation; Emiliania huxleyi; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; Growth rate, standard deviation; Haptophyta; Laboratory experiment; Laboratory strains; Maximum quantum yield of photosystem II; Maximum quantum yield of photosystem II, standard deviation; Net photosynthesis rate, per cell; Net photosynthesis rate, 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); Pelagos; pH; pH, standard deviation; Phytoplankton; Potentiometric; Potentiometric titration; Primary production/Photosynthesis; Registration number of species; Repair/damage ratio; Repair/damage ratio, standard deviation; Salinity; Single species; Species; Temperature, water; Treatment; Type; Uniform resource locator/link to reference  (1)
Document type
Keywords
Language
Years
  • 1
    Online Resource
    Online Resource
    Newark :John Wiley & Sons, Incorporated,
    Keywords: Aquatic plants - Ecophysiology. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (224 pages)
    Edition: 1st ed.
    ISBN: 9781118803448
    DDC: 572.46
    Language: English
    Note: Intro -- Photosynthesis in the Marine Environment -- Contents -- Photosynthesis in theMarine Environment -- About the authors -- Contributing authors -- Preface -- About the companion website -- Part I Plants and the Oceans -- Introduction -- Chapter 1 The evolution of photosynthetic organisms in the oceans -- Chapter 2 The different groups of marine plants -- 2.1 Cyanobacteria -- 2.2 Eukaryotic microalgae -- 2.3 Photosymbionts -- 2.4 Macroalgae -- 2.4.1 The green algae -- 2.4.2 The brown algae -- 2.4.3 The red algae -- 2.5 Seagrasses -- Chapter 3 Seawater as a medium for photosynthesis and plant growth -- 3.1 Light -- 3.2 Inorganic carbon -- 3.2.1 pH -- 3.3 Other abiotic factors -- 3.3.1 Salinity -- 3.3.2 Nutrients -- 3.3.3 Temperature -- 3.3.4 Water velocities -- Summary notes of Part I -- Part II Mechanisms of Photosynthesis, and Carbon Acquisition in Marine Plants -- Introduction to Part II -- Chapter 4 Harvesting of light in marine plants: The photosynthetic pigments -- 4.1 Chlorophylls -- 4.2 Carotenoids -- 4.3 Phycobilins -- Chapter 5 Light reactions -- 5.1 Photochemistry: excitation, de-excitation, energy transfer and primary electron transfer -- 5.2 Electron transport -- 5.3 ATP formation -- 5.4 Alternative pathways of electron flow -- Chapter 6 Photosynthetic CO2-fixation and -reduction -- 6.1 The Calvin Cycle -- 6.2 CO2-concentrating mechanisms -- Chapter 7 Acquisition of carbon in marine plants -- 7.1 Cyanobacteria and microalgae -- 7.1.1 Cyanobacteria -- 7.1.2 Eukaryotic microalgae -- 7.2 Photosymbionts -- 7.3 Macroalgae -- 7.3.1 Use of HCO3 -- 7.3.2 Mechanisms of HCO3- use -- 7.3.3 Rubisco and macroalgal photosynthesis: The need for a CO2 concentrating mechanism -- 7.4 Seagrasses -- 7.4.1 Use of HCO3- -- 7.4.2 Mechanisms of HCO3-use -- 7.5 Calcification and photosynthesis -- Summary notes of Part II. , Part III Quantitative Measurements, and Ecological Aspects, of Marine Photosynthesis -- Introduction to Part III -- Chapter 8 Quantitative measurements -- 8.1 Gas exchange -- 8.2 How to measure gas exchange -- 8.3 Pulse amplitude modulated (PAM) fluorometry -- 8.3.1 Quantum yields -- 8.3.2 Fv∕Fm -- 8.3.3 Electron transport rates -- 8.4 How to measure PAM fluorescence -- 8.4.1 Macrophytes -- 8.4.2 Microalgae -- 8.5 What method to use: Strengths and limitations -- 8.5.1 Rapid light curves -- 8.5.2 Fv∕Fm -- 8.5.3 Alpha, "uses and misuses" -- 8.5.4 Using whole plants -- Chapter 9 Photosynthetic responses, acclimations and adaptations to light -- 9.1 Responses of high and low-light plants to irradiance -- 9.2 Light responses of cyanobacteria and microalgae -- 9.3 Light effects on photosymbionts -- 9.4 Adaptations of Carbon acquisition mechanisms to light -- 9.5 Acclimations of seagrasses to high and low irradiances -- Chapter 10 Photosynthetic acclimations and adaptations to stress in the intertidal -- 10.1 Adaptations of macrophytes to desiccation -- 10.1.1 The ever-tolerant Ulva -- 10.1.2 The intertidal Fucus -- 10.1.3 The extremely tolerant Porphyra -- 10.1.4 Acclimations of seagrasses to desiccation (or not) -- 10.2 Other stresses in the intertidal -- Chapter 11 How some marine plants modify the environment for other organisms -- 11.1 Epiphytes and other 'thieves' -- 11.2 Ulva can generate its own empires -- 11.3 Seagrasses can alter environments for macroalgae and vice versa -- 11.4 Cyanobacteria and eukaryotic microalgae -- Chapter 12 Future perspectives on marine photosynthesis -- 12.1 'Harvesting' marine plant photosynthesis -- 12.2 Predictions for the future -- 12.3 Scaling of photosynthesis towards community and ecosystem production -- Summary notes of Part III -- References -- Index.
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  • 2
    Online Resource
    Online Resource
    Singapore :Springer,
    Keywords: Environmental chemistry. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (340 pages)
    Edition: 1st ed.
    ISBN: 9789811553547
    DDC: 577.14
    Language: English
    Note: Intro -- Preface -- Contents -- About the Editors -- Part I: Measurement of Environmental Parameters Affecting Marine Plankton Physiology -- Chapter 1: Characteristics of Marine Chemical Environment and the Measurements and Analyses of Seawater Carbonate Chemistry -- 1.1 Dissolved Inorganic Carbon -- 1.2 Total Alkalinity -- 1.3 pH -- 1.4 Seawater Partial Pressure of CO2 -- 1.5 Carbonate Mineral Saturation State -- 1.6 Determination of Seawater Carbonate System Parameters -- Chapter 2: Photosynthetically Active Radiation and Ultraviolet Radiation Measurements -- 2.1 Introduction -- 2.1.1 Light Intensity Measurement -- 2.1.2 Light Absorption and Extinction Coefficient -- 2.1.3 Planer and Spherical Radiometer Calibration -- References -- Part II: Plankton Culture Techniques -- Chapter 3: Manipulation of Seawater Carbonate Chemistry -- 3.1 Changes in the Carbonate Chemistry in Algal Cultures -- 3.2 Perturbation and Controlling of Seawater Carbonate Chemistry Parameters -- 3.2.1 Altering Concentration of Dissolved Inorganic Carbon -- 3.2.1.1 Controlling CO2 Partial Pressures -- 3.2.1.2 Adding CO2 Saturated Sea Water -- 3.2.1.3 Adding Strong Acid and CO32- or/and HCO3- -- 3.2.2 Changing Total Alkalinity -- 3.2.2.1 Adding Strong Acid and Alkali -- 3.2.2.2 Adding CO32- or/and HCO3- -- 3.2.2.3 Controlling Concentration of Ca2+ -- 3.3 Control of Microalgal Cell Density or Biomass -- 3.4 Analyses of Advantages and Disadvantages -- 3.5 Recommendations and Suggestions -- 3.5.1 Filtration and Sterilization -- 3.5.2 Maintain Carbonate Chemistry -- 3.5.3 Effects of Dissolved Organic Matters, Inorganic Nutrients, and Buffers on TA -- 3.5.4 The Treatment of Isotope Inorganic Carbon -- 3.5.5 Determination of Carbonate System Parameters -- 3.5.6 Measurement of pH -- References -- Chapter 4: Microalgae Continuous and Semi-continuous Cultures -- 4.1 Introduction. , 4.2 Microalgal Continuous Culture -- 4.2.1 Turbidostat -- 4.2.2 Chemostat -- 4.3 Microalgal Semicontinuous Culture -- 4.4 The Specific Growth Rates Calculation -- 4.4.1 Batch Culture -- 4.4.2 Semicontinuous Culture -- 4.4.3 Continuous Culture -- 4.5 Relative Merits and Optimization Recommendations -- 4.5.1 Relative Merits of Continuous Culture -- 4.5.2 The Advantages and Disadvantages of Microalgae Semicontinuous Cultures -- 4.5.3 Details in Culture Optimizing -- References -- Chapter 5: Culturing Techniques for Planktonic Copepods -- 5.1 Introduction -- 5.2 Copepod Culturing Methods -- 5.3 Procedures for Copepod Culture -- 5.3.1 Provenance Copepod Collection -- 5.3.2 Copepod Isolation, Purification and Culture -- 5.3.3 Feeding Food -- 5.3.4 Water Quality Control of Culture Medium -- 5.3.5 Harvesting -- 5.4 The Advantages and Disadvantages of Different Culture Methods and Points for Attention -- References -- Part III: Determination of Key Enzymes in Primary Producers -- Chapter 6: Carbonic Anhydrase -- 6.1 Introduction -- 6.2 Immunochemical Quantitative Analysis of Carbonic Anhydrase -- 6.2.1 Preparation of a Protein Sample of Carbonic Anhydrase -- 6.2.2 Separation of Proteins by Electrophoresis (Bailly and Coleman 1988 -- Zhao 2008) -- 6.2.2.1 Sample Treatment -- 6.2.2.2 Loading Sample and Electrophoresis -- 6.2.3 Transfer Proteins to Membrane -- 6.2.4 Blocking -- 6.2.5 Primary Antibody Incubation -- 6.2.6 Secondary Antibody Incubation -- 6.2.7 Protein Detection -- 6.3 Determination of Activity of Carbonic Anhydrase (Willbur and Anderson 1948 -- Xia and Huang 2010) -- 6.3.1 Measurement of Extracellular CA -- 6.3.2 Measurement of Intracellular CA -- 6.3.3 Advantage and Disadvantage -- References -- Chapter 7: Rubisco -- 7.1 Introduction -- 7.2 Experimental Materials and Methods -- 7.2.1 Protein Extraction. , 7.2.1.1 Extraction of Denatured Total Protein -- Materials, Reagents, Instruments and Experimental Methods -- 7.2.1.2 Extraction of Soluble Native Protein -- Materials, Reagents, Instruments, and Experimental Methods -- 7.2.2 Quantification of Rubisco -- 7.2.2.1 Rubisco Quantification Using Immunochemical Methods -- Materials, Reagents, Instruments, and Experimental Methods -- 7.2.2.2 Quantitative Rubisco Using 14C-CABP (2-Carboxy-d-arabinitol-1,5-bisphosphate) -- Materials, Reagents, Instruments, and Experimental Methods -- 7.2.3 Detection of Rubisco Activity -- 7.2.3.1 Detection of Rubisco Enzyme Activity Using NaH14CO3 -- Materials, Reagents, Instruments, and Experimental Methods -- 7.2.3.2 Enzyme-Linked Method of Detection of Rubisco Enzyme Activity -- Materials, Reagents, Instruments, and Experimental Methods -- 7.3 Advantages, Disadvantages, and Misunderstanding -- References -- Chapter 8: Phosphoenolpyruvate Carboxylase -- 8.1 PEPC and C4 Pathway -- 8.2 Preparation and Assay of PEPC -- 8.2.1 Preparation of Reagents -- 8.2.2 Preparation of Cell Extract -- 8.2.3 Procedure -- 8.2.4 14C Isotope Assay Methods -- 8.3 Note -- References -- Chapter 9: Nitrate Reductase -- 9.1 Introduction -- 9.2 Materials and Method -- 9.2.1 Materials -- 9.2.2 Reagent Preparation -- 9.2.3 Methods -- 9.3 Discussion -- References -- Chapter 10: Antioxidants and Reactive Oxygen Species (ROS) Scavenging Enzymes -- 10.1 Introduction -- 10.2 Superoxide Dismutase (SOD) Activity -- 10.2.1 Materials -- 10.2.2 Reagent Preparation -- 10.2.3 Methods -- 10.3 Catalase (CAT) Activity -- 10.3.1 Materials -- 10.3.2 Reagent Preparation -- 10.3.3 Methods -- 10.4 Peroxidase (POD) Activity -- 10.4.1 Materials -- 10.4.2 Reagent Preparation -- 10.4.3 Methods -- 10.5 Ascorbate Peroxidase (APX) Activity -- 10.5.1 Materials -- 10.5.2 Reagent Preparation -- 10.5.3 Methods. , 10.6 Glutathione Reductase (GR) Activity -- 10.6.1 Methods -- 10.7 Discussion -- References -- Part IV: Measurements and Analyses of Pigments -- Chapter 11: Chlorophylls -- 11.1 Distribution, Structure, and Spectral Characteristics of Chlorophylls -- 11.2 Quantitative Analysis of Chlorophyll -- 11.2.1 Spectrophotometry -- 11.2.2 High Performance Liquid Chromatography (HPLC) -- 11.3 The Advantages and Disadvantages of These Methods -- References -- Chapter 12: Phycobiliproteins -- 12.1 Quantitative Analysis of Phycobiliprotein -- 12.2 Isolation and Purification of Phycobiliprotein -- 12.3 Advantages and Disadvantages of Extraction Methods -- References -- Chapter 13: Carotenoids -- 13.1 Distribution of Carotenoids in the Algal Class -- 13.2 Carotenoid Analysis by HPLC -- 13.3 Quantification of Total Carotenoids -- 13.4 Note -- References -- Chapter 14: Phenolic Compounds and Other UV-Absorbing Compounds -- 14.1 Introduction -- 14.2 Determination of Phenolic Compounds -- 14.2.1 Spectrophotometer -- 14.2.2 HPLC -- 14.2.2.1 Preparation of Microalgae Extracts for Isolation and Quantification of Phenolic Compounds -- 14.2.2.2 Solid-Phase Extraction -- 14.2.2.3 Quantification of the Phenolic Compounds -- 14.2.3 Strengths and Limitations -- 14.3 Determination of UV-Absorbing Compounds -- 14.3.1 Extraction of Samples for HPLC Analysis of Mycosporine Amino Acids -- 14.3.2 HPLC Analysis -- References -- Part V: Measurements and Analyses of Photosynthesis and Respiration -- Chapter 15: Photosynthetic Oxygen Evolution -- 15.1 Instruments and Equipment -- 15.2 Solution Preparation -- 15.3 Operation Procedures -- 15.3.1 Installation of the Liquid Oxygen Electrode -- 15.3.2 Calibration of the Liquid Oxygen Electrode -- 15.3.3 Determination of Dissolved Oxygen -- 15.3.4 Calculation of Oxygen Evolution/Oxygen Consumption Rate of Samples. , 15.4 The Advantages, Disadvantages, and Considerations -- References -- Chapter 16: Photosynthetic Carbon Fixation -- 16.1 Introduction -- 16.2 14C Isotope Tracer Method -- 16.2.1 Sampling Protocols -- 16.2.2 14C Inoculation and Incubation -- 16.2.3 14C Collection, Treatment, and Measurement -- 16.3 Matters Needing Attention -- 16.3.1 Volume of Incubation Flask -- 16.3.2 Amount of 14C Addition -- 16.3.3 Incubation Time -- 16.4 Advantages and Disadvantages of the 14C Method -- 16.5 Application of the 14C Method in the Laboratory -- References -- Chapter 17: Photorespiration and Dark Respiration -- 17.1 Introduction -- 17.2 Materials and Methods -- 17.2.1 Algal Materials -- 17.2.2 Instruments -- 17.2.3 Method -- References -- Chapter 18: Carbon Dioxide vs. Bicarbonate Utilisation -- 18.1 Introduction -- 18.2 Methodology -- 18.2.1 Isotope Disequilibria -- 18.2.2 pH Dependence of K0.5 Values -- 18.2.3 Photosynthetic Rates at Different pH Values -- 18.2.3.1 Kinetics of O2 Evolution vs. Uncatalyzed CO2 Supply from HCO3- -- 18.2.3.2 MIMS -- 18.3 Merits and Demerits -- References -- Chapter 19: Action Spectra of Photosynthetic Carbon Fixation -- 19.1 Introduction -- 19.2 Action Spectrum of Visible Light -- 19.2.1 Absorption Spectrum of Pigment -- 19.2.2 Production of Action Spectrum -- 19.3 Biological Weighting Function of UV Radiation -- 19.3.1 Sample Collection -- 19.3.2 Solar Radiation Monitoring -- 19.3.3 Ultraviolet Radiation Treatment -- 19.3.4 Determination of Photosynthetic Carbon Fixation Rate -- 19.3.5 Calculation of BWF -- 19.3.5.1 Photosynthetic Carbon Fixation of Phytoplankton -- 19.3.5.2 UV Intensity Between Filters -- 19.3.5.3 Calculation of Biological Weight -- 19.4 Advantages and Disadvantages -- References -- Chapter 20: Determination of the Inorganic Carbon Affinity and CO2 Concentrating Mechanisms of Algae -- 20.1 Introduction. , 20.2 Determination of Inorganic Carbon Affinity.
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  • 3
    Publication Date: 2024-03-15
    Description: While seawater acidification induced by elevated CO2 is known to impact coccolithophores, the effects in combination with decreased salinity caused by sea ice melting and/or hydrological events have not been documented. Here we show the combined effects of seawater acidification and reduced salinity on growth, photosynthesis and calcification of Emiliania huxleyi grown at 2 CO2 concentrations (low CO2 LC:400 μatm; high CO2 HC:1000 μatm) and 3 levels of salinity (25, 30, and 35 per mil). A decrease of salinity from 35 to 25 per mil increased growth rate, cell size and photosynthetic performance under both LC and HC. Calcification rates were relatively insensitive to salinity though they were higher in the LC-grown compared to the HC-grown cells at 25 per mil salinity, with insignificant differences under 30 and 35 per mil. Since salinity and OA treatments did not show interactive effects on calcification, changes in calcification: photosynthesis ratios are attributed to the elevated photosynthetic rates at lower salinities, with higher ratios of calcification to photosynthesis in the cells grown under 35 per mil compared with those grown at 25 per mil. In contrast, photosynthetic carbon fixation increased almost linearly with decreasing salinity, regardless of the pCO2 treatments. When subjected to short-term exposure to high light, the low-salinity-grown cells showed the highest photochemical effective quantum yield with the highest repair rate, though the HC treatment enhanced the PSII damage rate. Our results suggest that, irrespective of pCO2, at low salinity Emiliania huxleyi up-regulates its photosynthetic performance which, despite a relatively insensitive calcification response, may help it better adapt to future ocean global environmental changes, including ocean acidification, especially in the coastal areas of high latitudes.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Bicarbonate ion; Bicarbonate ion, standard deviation; Bottles or small containers/Aquaria (〈20 L); Calcification/Dissolution; Calcification rate, standard deviation; Calcification rate/Photosynthesis rate, ratio; Calcification rate/Photosynthesis rate, ratio, standard deviation; Calcification rate of carbon per cell; 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 ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, standard deviation; Carotenoids, standard deviation; Carotenoids per cell; Cell, diameter; Cell, diameter, standard deviation; Chlorophyll a, standard deviation; Chlorophyll a per cell; Chlorophyll c, standard deviation; Chlorophyll c per cell; Chromista; Effective quantum yield; Effective quantum yield, standard deviation; Emiliania huxleyi; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; Growth rate, standard deviation; Haptophyta; Laboratory experiment; Laboratory strains; Maximum quantum yield of photosystem II; Maximum quantum yield of photosystem II, standard deviation; Net photosynthesis rate, per cell; Net photosynthesis rate, 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); Pelagos; pH; pH, standard deviation; Phytoplankton; Potentiometric; Potentiometric titration; Primary production/Photosynthesis; Registration number of species; Repair/damage ratio; Repair/damage ratio, standard deviation; Salinity; Single species; Species; Temperature, water; Treatment; Type; Uniform resource locator/link to reference
    Type: Dataset
    Format: text/tab-separated-values, 456 data points
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