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  • 1
    Online Resource
    Online Resource
    Dordrecht :Springer Netherlands,
    Keywords: Algae--Physiology. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (498 pages)
    Edition: 1st ed.
    ISBN: 9789400710382
    Series Statement: Advances in Photosynthesis and Respiration Series ; v.14
    DDC: 572/.46298
    Language: English
    Note: Photosynthesis in Algae -- Advances in Photosynthesis and Respiration VOLUME 14 -- Editor's page -- Copyright -- Editorial -- Contents -- Preface -- Color Plates -- Chapter 1 The Algae and their General Characteristics -- Chapter 2 Algal Plastids: Their Fine Structure and Properties -- Chapter 3 The Photosynthetic Apparatus of Chlorophyll b-and d-Containing Oxyphotobacteria -- Chapter 4 Structure and Regulation of Algal Light-Harvesting Complex Genes -- Chapter 5 Functional Analysis of Plastid Genes through Chloroplast Reverse Genetics in Chlamydomonas -- Chapter 6 Biochemistry and Regulation of Chlorophyll Biosynthesis -- Chapter 7 Oxygenic Photosynthesis in Algae and Cyanobacteria: Electron Transfer in Photosystems I and II -- Chapter 8 Oxygen Consumption: Photorespiration and Chlororespiration -- Chapter 9 The Water-Water Cycle in Algae -- Chapter 10 Carbohydrate Metabolism and Respiration in Algae -- Chapter 11 Carbon Acquisition Mechanisms of Algae: Carbon Dioxide Diffusion and Carbon Dioxide Concentrating Mechanisms -- Chapter 12 Modeling the Excitation Energy Capture in Thylakoid Membranes -- Chapter 13 Light-Harvesting Systems in Algae -- Chapter 14 Red, Cryptomonad and Glaucocystophyte Algal Phycobiliproteins -- Chapter 15 Carotenoids of Light Harvesting Systems: Energy Transfer Processes from Fucoxanthin and Peridinin to Chlorophyll -- Chapter 16 Photoinhibition, UV-B and Algal Photosynthesis -- Chapter 17 Adaptation, Acclimation and Regulation in Algal Photosynthesis -- Chapter 18 Photosynthesis in Marine Macroalgae -- Chapter 19 Photosynthesis in Symbiotic Algae -- Index.
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  • 2
    Online Resource
    Online Resource
    Cham :Springer International Publishing AG,
    Keywords: Algae-Physiology. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (534 pages)
    Edition: 1st ed.
    ISBN: 9783030333973
    Series Statement: Advances in Photosynthesis and Respiration Series ; v.45
    Language: English
    Note: Intro -- Copyright -- From the Series Editors -- Authors of Volume 45 -- Our Books -- Series Editors -- Contents -- Preface: A Brief Introduction to the Algae -- The Evolution of Photosynthesis -- The Evolution of Algae -- The Evolution of Eukaryotic Algae -- About the Editors -- Contributors -- Author Index -- Part I: Introductory Chapters -- Chapter 1: Recent Advances in the Photosynthesis of Cyanobacteria and Eukaryotic Algae -- I. Algal Systematics -- II. Cyanobacteria -- III. Crystal Structures -- IV. Light Harvesting -- V. Photoinhibition -- VI. Dinoflagellates and Coral Bleaching -- VII. Carbon Uptake and Metabolism (See Chap. 7 & -- 8) -- VIII. Water-Water Cycles (See Chap. 8) -- References -- Chapter 2: The Algal Tree of Life from a Genomics Perspective -- I. Introduction -- II. Why Inferring the Algal Tree of Life Is Non-trivial -- III. Examples of Reticulate Behavior Among Algal Genes -- IV. From Designer Datasets to Whole Genomes -- V. Conclusions -- Acknowledgments -- References -- Part II: Molecular Genetics of Algae -- Chapter 3: Chlorophyll-Xanthophyll Antenna Complexes: In Between Light Harvesting and Energy Dissipation -- I. Introduction -- II. Chromophores -- III. The Core Complexes of PSII and PSI -- IV. Light Harvesting -- A. Type I (LHCBM3, 4, 6, 8 and 9) -- B. Type II (LHCBM5) -- C. Type III (LHCBM2 and 7) -- D. Type IV (LHCBM1) -- V. Antenna Complexes of PSI -- VI. Fucoxanthin Chlorophyll Binding Proteins -- VII. Photoprotection -- VIII. Triggers of Quenching Reactions -- IX. Conclusions -- Acknowledgements -- References -- Chapter 4: The Dynamics of the Photosynthetic Apparatus in Algae -- I. Introduction -- II. Adaptation to Changes in Light Conditions -- A. State Transitions -- B. Non Photochemical Quenching (NPQ) -- C. PSII Repair Cycle. , III. Response of the Photosynthetic Apparatus to Micronutrient Depletion -- A. Copper Deficiency -- B. Iron Deficiency -- C. Sulfur Deprivation and Hydrogen Production -- D. Nitrogen Deprivation -- IV. Long Term Response: Changes in Nuclear and Chloroplast Gene Expression -- V. Conclusions and Perspectives -- Acknowledgements -- References -- Chapter 5: Biosynthesis of Chlorophyll and Bilins in Algae -- I. Introduction -- II. Diversity of Chlorophylls in Algae -- III. Diversity of Bilins in Algae -- IV. Overview of Biosynthesis of Bilins and Chlorophylls -- V. Biosynthesis of Protoporphyrin IX -- VI. Biosynthesis of Bilins from Protoporphyrin and Function of Bilin Lyases -- VII. Biosynthesis of Chlorophylls from Protoporphyrin IX -- VIII. Synthesis of Chlorophyll b, d and f -- IX. Concluding Remarks -- Bibliography -- Part III: Biochemistry and Physiology of Algae -- Chapter 6: Chloroplast Ion and Metabolite Transport in Algae -- I. Introduction -- II. Chloroplast Ion Transport -- A. Ion Channels -- 1. Voltage-Dependent Chloride Channels -- 2. Mechanosensitive Ion Channels -- 3. K+ Channels -- 4. Ca2+ Channels -- B. Ion Transporters -- 1. Phosphate Transporters -- 2. Sulfate Transporters -- 3. Nitrite Transporters -- 4. Potassium Proton Exchangers -- 5. Manganese and Calcium Transporters -- 6. Magnesium Transporters -- 7. Iron Transporters -- C. Ion Pumps (P-ATPases) -- D. ABC Transporters -- III. Chloroplast Metabolite Transport -- A. ATP Transporters -- 1. Plastidic Nucleotide Translocators -- 2. The Thylakoid ATP/ADP Carrier -- B. Plastidic Phosphate Transporters -- 1. Triose-Phosphate Transporters -- 2. Phosphoenolpyruvate Transporters -- 3. Glucose-6-Phosphate and Xylulose-5-Phosphate Translocators -- C. Bicarbonate Transporters -- D. Organic Acid Transporters -- E. Amino Acid Transporters -- F. Fatty Acid Transporters. , G. Lipid ABC Transporters -- IV. Strategies for Identification of Missing Algal Transporters -- V. Conclusions and Perspectives -- References -- Chapter 7: Structural and Biochemical Features of Carbon Acquisition in Algae -- I. Introduction -- II. Carbon Assimilation -- A. The Characteristics of Most Rubiscos Necessitate Operation of a CCM -- B. The PCRC and Other Pathways for C Assimilation -- III. Occurrence of CCMs -- IV. Mechanisms of CCMs Versus Diffusive CO2 Fluxes -- A. Definition of CCMs and What Do We Need in Order to Demonstrate Operation of CCMs? -- B. CCMs Based on Active Transport of Inorganic C Species -- C. C4 Photosynthesis as a CCM in Algae? -- V. Structural Aspects of CO2 Acquisition -- Acknowledgements -- References -- Chapter 8: Light-Driven Oxygen Consumption in the  Water-Water Cycles and Photorespiration, and Light Stimulated Mitochondrial Respiration -- I. Introduction -- II. The Evidence of Light-Dependent O2 Uptake -- III. Possible Mechanisms of Light-Driven O2 Uptake -- A. Water-Water Cycles -- B. The Mehler Ascorbate Peroxidase (MAP) Reactions Involving PSI and PSII -- C. Flavodiiron Protein Involving PSI and PSII -- D. Plastid (Plastoquinol) Terminal Oxidase (PTOX) Involving PSII but not PSI -- E. Photorespiration -- F. Mitochondrial Respiration -- G. Allocation of O2 Uptake Among the Five Pathways -- IV. Functions of the Light-Driven O2 Uptake Processes -- V. Conclusions -- Acknowledgements -- References -- Chapter 9: The Algal Pyrenoid -- I. Introduction -- A. A Pyrenoid Timeline - From Microscopic Curiosity to a Key Factor in the Earth's Carbon Cycle -- B. Pyrenoid Prevalence -- C. Independent Origins but Convergent Structures -- D. Diversity -- II. Pyrenoid Structure & -- Function: Lessons from Chlamydomonas -- A. Structure and Organisation. , B. Functional Integration of Pyrenoid Proteome and CCM Activity -- C. Integrating Transcriptomics and Pyrenoid-Associated Processes -- III. When, Where, How and Whither: From Paleo-Origins to Future Synthetic Biology -- References -- Part IV: Light-Harvesting Systems in Algae -- Chapter 10: Light-Harvesting in Cyanobacteria and Eukaryotic Algae: An Overview -- I. Introduction -- II. The Photosynthetic Pigments of Cyanobacteria and Eukaryotic Algae -- A. Chlorophylls -- 1. Chlorophyll a -- 2. Chlorophyll b -- 3. Chlorophyll c and MgDVD -- 4. Chlorophyll d -- 5. Chlorophyll f -- 6. Summary Comments on the Chlorophylls -- B. Carotenoids -- 1. Carotenes -- 2. Xanthophylls -- C. Phycobiliproteins -- III. The Evolution of Protists with Plastids (Algae) -- A. Algae with Primary Plastids -- 1. Glaucophyceae -- 2. Rhodophyceae -- 3. Chlorophyceae -- B. Secondary and Tertiary Plastids -- 1. Diatoms (Bacillariophyceae) and Related Phyla Including the Phaeophyceae -- 2. Related Phyla -- 3. Dinoflagellates -- 4. Cryptophytes (Cryptophyceae) -- 5. Other Stramenopiles, Haptophytes and Apicomplexans -- IV. The Need for Light-Harvesting Antennas -- V. Light-Harvesting Antennas in Cyanobacteria and Eukaryotic Algae -- VI. Control of Energy Supply to PSI and PSII: State Transitions, Absorption Cross-Sectional Changes and Spillover -- A. Overview -- B. State Transitions -- 1. State Transitions in Chlamydomonas -- 2. An Aside on Cyclic Electron Transport (CET) -- 3. State Transitions in Other Algae -- C. Absorption Cross-Sectional Changes -- D. Spillover -- E. Complementary Chromatic Adaptation -- F. Non-photochemical Quenching - Sensu Lato -- VII. Non-photochemical Quenching -- A. The Xanthophyll Cycle -- B. pH Quenching -- C. Orange Carotenoid Protein -- VIII. Reactive Oxygen Species (ROS) and Other Photoprotective Mechanisms -- Acknowledgements. , References -- Chapter 11: Light Harvesting by Long-Wavelength Chlorophyll Forms (Red Forms) in Algae: Focus on their Presence, Distribution and Function -- I. Long Wavelength ("Red") Chlorophyll a Forms: Historical Perspective on Their Discovery and General Overview -- II. Long Wavelength Chlorophyll Forms Associated to Photosystem I -- A. Photosystem I Core Red Forms -- B. Photosystem I External Antenna Red Forms -- C. Nature of Long Wavelength Chlorophyll Forms -- III. Long Wavelength Chlorophyll Forms Associated to Photosystem II -- A. PSII-Associated Long Wavelength Chlorophylls in Algae -- IV. Survey of Cyanobacterial and Algal Species for the Presence of Long-Wavelength Chlorophyll Forms -- A. Physiological and Environmental Consequences of the Presence of Red Forms (or Their Absence) -- V. Effect of Long Wavelength Chlorophyll Forms on the Photochemical Quantum Efficiency -- A. Simulations of the Impact of Red Forms on Excited State Energy Trapping -- 1.. Photosystem I -- 2.. Photosystem II -- VI. Concluding Remarks -- Acknowledgements -- References -- Chapter 12: Diversity in Photoprotection and Energy Balancing in Terrestrial and Aquatic Phototrophs -- I. Introduction -- II. Energy Storage and Regulation in Oxygenic Photosynthesis -- III. The pmf Paradigm for Regulation of the Photosynthetic Light Reactions -- IV. The Need to Coordinate qE and Photosynthetic Control -- V. The Critical Need to Balance the Chloroplast Energy Budget -- VI. Regulation of CEF -- VII. Modulation of pmf Feedback Regulation and Its Impact on Energy Balancing -- VIII. How Diverse Photoprotective Mechanisms Challenge the pmf Paradigm and Open Up New Questions -- IX. Coping with ATP Excess or NADPH Deficit -- A. Energy Balancing by Interactions Between Photosynthetic and Respiratory Machinery -- X. Conclusions and Perspective -- Acknowledgements. , References.
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  • 3
    Book
    Book
    New York, NY : Liss
    Keywords: Aufsatzsammlung ; Wasserpflanzen ; Bioenergetik ; Wasserpflanzen ; Stofftransport ; Bioenergetik ; Wasserpflanzen ; Wasserpflanzen ; Pflanzenphysiologie
    Type of Medium: Book
    Pages: IX, 587 S. , graph. Darst.
    ISBN: 0845122037
    Series Statement: MBL lectures in biology 4
    DDC: 581.1
    RVK:
    Language: English
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  • 4
    Online Resource
    Online Resource
    Cham : Springer
    Keywords: Microalgae Biotechnology ; Microalgae Cultures and culture media
    Description / Table of Contents: This book covers the state-of-the-art of microalgae physiology and biochemistry (and the several -omics). It serves as a key reference work for those working with microalgae, whether in the lab, the field, or for commercial applications. It is aimed at new entrants into the field (i.e. PhD students) as well as experienced practitioners. It has been over 40 years since the publication of a book on algal physiology. Apart from reviews and chapters no other comprehensive book on this topic has been published. Research on microalgae has expanded enormously since then, as has the commercial exploitation of microalgae. This volume thoroughly deals with the most critical physiological and biochemical processes governing algal growth and production
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource
    Edition: Online-Ausg.
    Series Statement: Developments in applied phycology 6
    Language: English
    Note: Includes bibliographical references
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  • 5
    Electronic Resource
    Electronic Resource
    Copenhagen : Munksgaard International Publishers
    Physiologia plantarum 113 (2001), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The Ingestad approach to the culture of higher terrestrial plants for physiological studies is discussed in relation to a number of resources, organisms and growth situations that were not part of the original design and rationale of Ingestad's methodology. The additional resource considered is photosynthetically active radiation, and difficulties of applying the Ingestad approach to this resource as well as to atmospheric CO2 are considered. The relationship of the Ingestad approach to reductionist studies based on enzyme kinetic studies is then briefly considered. The organisms considered next are aquatic plants, including both micro- and macrophytes. The consideration of photosynthetic microorganisms leads to a comparison of the Ingestad approach with growth in batch, and in continuous (chemostat and turbidostat) cultures, and with studies on growth in synchronous cultures in which cyclic changes in cell composition in the cell growth and division cycle can be identified. The natural environmental conditions for these organisms are a natural extension of the light/dark synchronization of laboratory cultures, and the bloom (batch culture equivalent to new production) and of grazing and parasitism removing biomass and recycling nutrients (chemostat or turbidostat culture equivalent to recycled production) situations for phytoplankton. The overall conclusion is that, while the Ingestad approach is a useful mirror in which to examine other concepts of plant resource acquisition and manipulation, the Ingestad methodology seems to make assumptions about the intrinsic growth rate and composition of plants that cannot be independently verified.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Plant, cell & environment 22 (1999), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: We grew a non-bicarbonate using red seaweed, Lomentaria articulata (Huds.) Lyngb., in media aerated with four O2 concentrations between 10 and 200% of current ambient [O2] and four CO2 concentrations between 67 and 500% of current ambient [CO2], in a factorial design, to determine the effects of gas composition on growth and physiology. The relative growth rate of L. articulata increased with increasing [CO2] up to 200% of current ambient [CO2] but was unaffected by [O2]. The relative growth enhancement, on a carbon basis, was 52% with a doubling of [CO2] but fell to 23% under 5× ambient [CO2]. Plants collected in winter responded more extremely to [CO2] than did plants collected in the summer, although the overall pattern was the same. Discrimination between stable carbon isotopes (Δ13C) increased with increasing [CO2] as would be expected for diffusive CO2 acquisition. Tissue C and N were inversely related to [CO2]. Growth in terms of biomass appeared to be limited by conversion of photosynthate to new biomass rather than simply by diffusion of CO2, suggesting that non-bicarbonate-using macroalgae, such as L. articulata, may not be directly analogous to C3 higher plants in terms of their responses to changing gas composition.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant, cell & environment 5 (1982), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract. The role of ‘slippage’ reactions, in the form of passive H+ uniport through CF0-CF1, ATP synthetase and breakdown of the S2 and S3 intermediates of O2 evolution, is considered in relation to the growth of phototrophic organisms at low photon fluence rates. Analysis of the limited data available suggests that adaptation (phenotypic or genotypic) to low photon fluence rates is accompanied by an increase in the ratio of light-absorbing pigments to the (potentially slippage-inducing) photosystem two units and CF0-CF1 ATP synthetases. Furthermore, organisms which are genotypically adapted to high photon fluence rates do not, when grown at low photon fluence rates, achieve the same low ratio of reaction centres to total light-harvesting pigments as is found in phototrophs genotypically adapted to low photon fluence rates. The limits to, and energy costs of, such a mechanism of adaptation to low photon fluence rates are also discussed.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 10 (1981), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1432-2048
    Keywords: Ammonia ; Cytosol (pH) ; C3 and C4 plants ; Dye (pH-indicating) ; Vacuole (pH)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Atmospheric ammonia (NH3) from various anthropogenic sources has become a serious problem for natural vegetation. Ammonia not only causes changes in plant nitrogen metabolism, but also affects the acid-base balance of plants. Using the pH-sensitive fluorescent dyes pyranine and esculin, cytosolic and vacuolar pH changes were measured in leaves of C3 and C4 plants exposed for brief periods to concentrations of NH3 in air ranging from 1.33 to 8.29 μmol NH3 · mol-1 gas (0.94–5.86 mg · m-3). After a lag phase, uptake of NH3 from air at a rate of 200 nmol NH3 · m - 2 leaf area · s- 1 into leaves of Zea mays L. increased pyranine fluorescence indicating cytosolic alkalinisation. The increase was much larger in the dark than in the light. In illuminated leaves of the C3 plant Pelargonium zonale L. and the C4 plants Z. mays and Amaranthus caudatus L., NH3-dependent cytosolic alkalinisation was particularly pronounced when CO2 was supplied at very low levels (16 or 20 μmol CO2 · mol- 1 gas, containing 210 mmol O2 · mol- 1 gas). An increase in esculin fluorescence, which was smaller than that of pyranine, was indicative of trapping of some of the NH3 in the vacuoles of leaves of Spinacia oleracea L. and Z. mays. Photosynthesis and transpiration remained unchanged during exposure of illuminated leaves to NH3, yielding an influx of 200 nmol NH3 · m-2 leaf area · s-1 for up to 30 min, the longest exposure time used. Both CO2 and O2 influenced the extent of cytosolic alkalinisation. At 500 μmol CO2 · mol-1 gas the cytosolic alkalinisation was suppressed more than at 16 or 20 μmol CO2 · mol-1 gas. The suppressing effect of CO2 on the NH3induced alkalinisation was larger in illuminated leaves of the C4 plants Z. mays and A. caudatus than in leaves of the C3 plant P. zonale. A reduction of the O2 concentration from 210 to 10 mmol O2 · mol -1 gas, which inhibits photorespiration, increased the NH3induced cytosolic alkalinisation in C3 plants. Suppression by CO2 or O2 of the alkaline pH shift caused by the dissolution and protonation of NH3 in queous leaf compartments, and possibly by the production of organic compounds synthesised from atmospheric NH3, indicates that NH3 which enters leaves is rapidly assimilated if photosynthesis or photorespiration provide nitrogen acceptor molecules.
    Type of Medium: Electronic Resource
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