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  • 1
    Online Resource
    Online Resource
    Dordrecht :Springer Netherlands,
    Keywords: Bioluminescence. ; Chlorophyll. ; Aquatic sciences--Research. ; Electronic books.
    Description / Table of Contents: This book follows on from the first international conference on "chlorophyll fluorescence in the aquatic sciences" (AQUAFLUO 2007). It offers the first complete synthesis of chlorophyll fluorescence methods for the aquatic sciences.
    Type of Medium: Online Resource
    Pages: 1 online resource (331 pages)
    Edition: 1st ed.
    ISBN: 9789048192687
    Series Statement: Developments in Applied Phycology Series ; v.4
    Language: English
    Note: Intro -- Chlorophyll a Fluorescence in Aquatic Sciences -- Preface -- Contents -- Contributors -- Chapter 1: Chlorophyll Fluorescence Terminology: An Introduction -- 1 Introduction -- 2 Light and Absorption -- 3 Fluorescence -- 3.1 Fast Phase (O-J-I-P) -- 3.1.1 Additional Features -- 3.2 Slow Phase (S-M-T) -- 3.3 The Saturation Pulse Method -- 3.4 Quantum Yield for PSII (FPSII) -- 3.5 Quenching -- 4 Conclusion -- References -- Chapter 2: In Situ Measurement of Variable Fluorescence Transients -- 1 Introduction -- 2 Phytoplankton Variable Fluorescence In Situ -- 2.1 Dynamical Protocols for Stimulating Variable Fluorescence -- 2.2 The Practical Relevance of the Single-turnover Time Scale In Situ -- 2.3 Issues Related to the Marine Light Field -- 2.4 Apparent Effects Resulting from Assemblage Composition -- 2.5 Effects Due to Optical Properties of Natural Waters -- 3 Conclusions and Future Directions -- References -- Chapter 3: Overview of Fluorescence Protocols: Theory, Basic Concepts, and Practice -- 1 Introduction -- 2 Theoretical Background -- 2.1 The Fluorescing Properties of Chlorophyll a -- 2.2 Source of Fluorescence in Seawater and Mathematical Description of Fluorescence Emission -- 2.3 The Functional Organization of the Photosynthetic Apparatus -- 2.3.1 Photosystem II -- 2.3.2 The Photosynthetic Chain -- 2.4 Adaptation, Acclimation, Regulation of Phytoplankton -- 2.5 Fates of Absorbed Photons Within PSII -- 2.6 A Simple Model of In Vivo Processes In PSII At Room Temperature -- 2.6.1 Quantum Yield of Fluorescence -- 2.7 Charge Separation at PSII -- 2.8 Photochemical Quenching of Fluorescence -- 2.9 Non-photochemical Quenching of Fluorescence -- 2.9.1 Energy-dependent Non-photochemical Quenching -- 2.9.2 Quenching Due to State Transitions -- 2.9.3 Quenching Linked to Inhibition -- 2.9.4 Reaction Center Quenching. , 2.10 Transient Changes in Fluorescence -- 3 Protocols for Measurement of In Vivo Phytoplankton Fluorescence, and the Use of Chl a Fluorescence to Study Phytoplankton -- 3.1 The Determination of Biomass In Vivo -- 3.1.1 Basic Principle -- 3.1.2 Instruments and Protocols -- 3.1.3 Validity of the Underlying Assumptions -- 3.1.4 Examples -- 3.2 Spectrofluorometry -- 3.2.1 Basic Principle -- 3.2.2 Instruments and Protocols -- 3.2.3 Validity of the Underlying Assumptions -- 3.2.4 Examples -- 3.3 Sun-induced Chlorophyll Fluorescence -- 3.3.1 Validity of the Underlying Assumptions -- 3.3.2 Examples -- 3.4 Flow Cytometry -- 3.5 Laser Excitation and LIDAR Fluorometry -- 3.6 Variable Fluorescence -- 3.6.1 Basic Principle -- 3.6.2 Instruments and Protocols -- Use of DCMU -- Pulse Amplitude Modulation -- Pump-and-Probe -- Fast Repetition Rate -- 3.6.3 Validity of the Underlying Assumptions -- 3.6.4 Examples -- 4 The Use of Chlorophyll Fluorescence to Estimate Primary Production -- 4.1 Variable Fluorescence -- 4.1.1 If is Available (FRRF and Pump and Probe Protocol) -- 4.1.2 When is not Available (PAM Protocol) -- 4.2 Sun-induced Chlorophyll Fluorescence -- 5 Conclusion -- 6 List of Symbols -- References -- Chapter 4: Fluorescence as a Tool to Understand Changes in Photosynthetic Electron Flow Regulation -- 1 Introduction -- 2 Electron Usage in Photosynthesis -- 2.1 Alternative Electron Cycling (AEC) -- 2.2 Electron Usage to Produce New Biomass -- 3 Effect of Light Stress on Fluorescence Signatures and their Interpretation -- 4 Use of Chemicals for the Differentiation of Photosynthetic Processes -- 4.1 Inhibitors of Linear Electron Transport -- 4.2 Inhibitors of Cyclic Electron Transport -- 4.3 Inhibitors of Alternative Electron Cycling (AEC) -- 4.4 Inhibitors of CO2 Fixation -- 4.5 Electron Transport Uncouplers -- 4.6 Electron Acceptors -- References. , Chapter 5: Microscopic Measurements of the Chlorophyll a Fluorescence Kinetics -- 1 Introduction -- 2 Fluorescence Techniques in High Resolution -- 3 Applications of Fluorescence Kinetic Microscopy -- References -- Chapter 6: Estimating Aquatic Productivity from Active Fluorescence Measurements -- 1 Fluorescence as a Probe for Photosynthesis -- 2 Overview of the Theory of Calculating ETRPSII -- 2.1 Measuring fPSII¢ and Calculating ETR -- 2.2 Examining Changes to the Quantum Yield Under Actinic Light -- 3 Light Absorption by Photosystem II -- 3.1 Bio-Physical Measures of PSII Absorption and Calculationof Chlorophyll-Specific ETR -- 3.2 Bio-Optical Based Determinationsof PSII Absorption -- 4 Reconciling Active Fluorescence-based Estimates of Productivity with Gas Exchange -- 4.1 Practical Constraints in Comparing Fluorescence- and Gas Exchange-Based Productivity Measurements -- 4.2 Are ETRs Indicative of Gross O2 Evolution? -- 4.3 Estimating Net O2 Production and C-Fixation from ETRs -- 4.4 Reconciliation of ETRPSII : O2 : CO2 Estimates -- 5 Future Application of ETRs to Primary Productivity Studies -- References -- Chapter 7: Taxonomic Discrimination of Phytoplankton by Spectral Fluorescence -- 1 Introduction -- 2 The Principles of Taxonomy by Spectral Fluorescence -- 2.1 Energy Transfer Between Pigments -- 2.2 Taxonomic Differences in Fluorescence Spectra -- 2.3 Taxonomic Discrimination by Spectral Fluorescence -- 3 Variation in Chlorophyll-specific Fluorescence, FChl -- 3.1 Inter-Specific Variability -- 3.2 Intra-specific Variability -- 3.3 Short-Term Quenching -- 4 Optical Indices and Application of the SFS Approach in the Field -- 4.1 Bias in SFS by Background Absorption and Scattering -- 4.2 Quenching In Situ and Taxonomic Assessment -- 5 A Field Test of the SFS Approach -- 6 Conclusion -- References. , Chapter 8: Flow Cytometry in Phytoplankton Research -- 1 Introduction -- 2 Background and Historical Perspective -- 3 Select Research Applications -- 3.1 Picophytoplankton Community Structure and Dynamics -- 3.2 Time Resolved Pulses for Physiological and Ecological Studies -- 3.3 Cell Sorting for Physiology and Diversity -- 3.4 Interpretation of Optical Variability in the Ocean -- 4 Emerging Approaches and Applications -- References -- Chapter 9: The Use of the Fluorescence Signal in Studies of Seagrasses and Macroalgae -- 1 Introduction -- 2 Major Achievements Using the Chlorophyll a Fluorescence Signal in Seagrass and Macroalgae Studies -- 2.1 Quenching Analysis -- 2.2 Analysis of Quenching Components: Use of Chemicals -- 3 Protocols Used, Limitations and Specific Modifications for Aquatic Macrophytes -- 3.1 Determination of the Variation in Fv/Fm and DF/Fm¢ -- 3.2 Limitation of the Use of Rapid Light Curves (RLC) -- 3.3 The Importance of Photosynthesis Induction -- 3.4 Determination of Absorptance, PSII Effective Absorption Cross-Section and the Number of Reaction Centers -- 3.5 Use of Relative ETR Values (rETR) -- 3.6 The Use of Electron Transport Rates Values (ETR) as Descriptors of Gross Photosynthesis (GPS) -- 4 Final Comments -- References -- Chapter 10: Chlorophyll Fluorescence in Reef Building Corals -- 1 Introduction -- 2 Natural Patterns of Fluorescence -- 2.1 Multiple and Single Turnover Instrumentation -- 2.2 Non-Photochemical Quenching -- 3 Detecting Stress -- 4 Protocols and Pitfalls -- 4.1 Dark Acclimation, Sample Area and Related Matters -- 4.2 Electron Transport Rate -- 5 Conclusion -- References -- Chapter 11: Assessing Nutrient Status of Microalgae Using Chlorophyll a Fluorescence -- 1 Introduction -- 2 Defining Nutrient Limitation -- 3 The Effects of Nutrient Limitation on Phytoplankton -- 3.1 Nitrogen -- 3.2 Phosphorus. , 3.3 Iron -- 4 Measuring Nutrient Limitation -- 4.1 Nutrient Enrichment Bioassays -- 4.2 Chlorophyll a Fluorescence as a Measure of Nutrient Stress -- 4.3 Natural Population Enrichments and Chlorophyll a Fluorescence -- 5 NIFTS -- 5.1 What is a NIFT? -- 5.2 How to Measure NIFTs -- 5.3 The Characteristics of the NIFT Response are Dependent on the Limiting Nutrient -- 5.4 NIFT Responses of Different Taxa -- 5.5 Mechanisms Behind NIFTs -- 6 Conclusion -- References -- Chapter 12: The Application of Variable Chlorophyll Fluorescence to Microphytobenthic Biofilms -- 1 Introduction to Benthic Biofilms -- 2 The Effects of Subsurface Signal -- 2.1 Microphytobenthic Biofilms on Soft Sediments -- 2.2 Stromatolites - the effect of "layered" biofilms -- 2.3 Deconvolution of Depth Integrated Signals -- 3 Down Regulation Through Non-photochemical Quenching -- 3.1 NPQ and the Xanthophyll Cycle in Diatoms -- 3.2 NPQ in the Dark -- 4 The Quantification of the Microalgal Biomass Using Fluorescence -- 5 Calculation of Electron Transport Rate: ETR v rETR -- 5.1 Multiple and Single Turnover Methods -- 5.2 The MT-method -- 5.3 The ST-method -- 5.4 Assumptions and Uncertainties -- 5.5 Calculation of ETR in Microphytobenthos Studies -- 6 Light Response Curves -- 6.1 A Brief Overview of Methodology -- 6.2 Steady State Light Curves -- 6.3 Rapid Light Curves -- 6.4 Non-sequential Light Curves -- 6.5 Light Curves Summary -- 7 Comparison of Fluorescence with Other Methodologies -- 8 General Summary -- References -- Chapter 13: Chlorophyll Fluorescence Applications in Microalgal Mass Cultures -- 1 Preface -- 2 Historical Overview of Using Chl Fluorescence in Microalgal Mass Cultures -- 3 Microalgae Grown for Commercial Purposes and Cultivation Systems -- 4 Principles of Microalgae Mass Culturing -- 4.1 Culture Maintenance. , 5 Interpretation of Chl Fluorescence Parameters in MicroalgaeMass Cultures.
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  • 2
    Keywords: Bioluminescence ; Chlorophyll ; Aquatic sciences Research ; Konferenzschrift ; Fluoreszenz ; Chlorophyll a ; Phytoplankton ; Mikroalgen
    Description / Table of Contents: "Measurements of variable chlorophyll fluorescence have revolutionised global research of photosynthetic bacteria, algae and plants and in turn assessment of the status of aquatic ecosystems, a success that has partly been facilitated by the widespread commercialisation of a suite of chlorophyll fluorometers designed for almost every application in lakes, rivers and oceans. Numerous publications have been produced as researchers and assessors have simultaneously sought to optimise protocols and practices for key organisms or water bodies; however, such parallel efforts have led to difficulties in reconciling processes and patterns across the aquatic sciences. This book follows on from the first international conference on "chlorophyll fluorescence in the aquatic sciences" (AQUAFLUO 2007) : to bridge the gaps between the concept, measurement and application of chlorophyll fluorescence through the synthesis and integration of current knowledge from leading researchers and assessors as well as instrument manufacturers."--P. [4] of cover
    Type of Medium: Book
    Pages: XVIII, 323 S. , Ill. (farb.), graph. Darst. , 260 mm x 193 mm
    ISBN: 9789048192670
    Series Statement: Developments in applied phycology 4
    DDC: 572/.46
    Language: English
    Note: Enth. Literaturangaben und Index
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  • 3
    ISSN: 1573-5079
    Keywords: absorption cross section of PS II ; chlorophyll fluorescence ; photoinhibition ; phytoplankton ; QA ; quantum efficiency of PS II ; UV radiation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The effects of PAR and UV radiation on PS II photochemistry were examined in natural phytoplankton communities from coastal waters off Rhode Island (USA) and the subtropical Pacific. The photochemical energy conversion efficiency, the functional absorption cross section and the kinetics of electron transfer on the acceptor side of PS II were derived from variable fluorescence parameters using both pump and probe and fast repetition rate techniques. In both environments, the natural phytoplankton communities displayed marked decreases in PS II photochemical energy conversion efficiency that were correlated with increased PAR. In the coastal waters, the changes in photochemical energy conversion efficiency were not statistically different for samples treated with supplementary UV-B radiation or screened to exclude ambient UV-B. Moreover, no significant light-dependent changes in the functional absorption cross section of PS II were observed. The rate of electron transfer between QA - and QB was, however, slightly reduced in photodamaged cells, indicative of damage on the acceptor side. In the subtropical Pacific, the decrease in photochemical energy conversion efficiency was significantly greater for samples exposed to natural levels of UV-A and/or UV-B compared with those exposed to PAR alone. The cells displayed large diurnal changes in the functional absorption cross section of PS II, indicative of non-photochemical quenching in the antenna. The changes in the functional absorption cross section were highly correlated with PAR but independent of UV radiation. The time course of changes in photochemical efficiency reveals that the photoinhibited reaction centers rapidly recover (within an hour or two) to their preillumination values. Thus, while we found definitive evidence for photoinhibition of PS II photochemistry in both coastal and open ocean phytoplankton communities, we did not find any effect of UV-B on the former, but a clear effect on the latter. The results of this study indicate that the effects of UV-B radiation on phytoplankton photosynthesis are as dependent on the radiative transfer properties of the water body and the mixing rate, as on the wavelength and energy distribution of the radiation and the absorption cross sections of the biophysical targets.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-5079
    Keywords: carbon fixation ; phytoplankton
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Exposure of algae or higher plants to bright light can result in a photoinhibitory reduction in the number of functional PS II reaction centers (n) and a consequential decrease in the maximum quantum yield of photosynthesis. However, we found that light-saturated photosynthetic rates (Pmax) in natural phytoplankton assemblages sampled from the south Pacific ocean were not reduced despite photoinhibitory decreases in n of up to 52%. This striking insensitivity of Pmax to photoinhibition resulted from reciprocal increases in electron turnover ( $${1 \mathord{\left/ {\vphantom {1 {\tau _{PSII} }}} \right. \kern-\nulldelimiterspace} {\tau _{PSII} }}$$ )through the remaining functional PS II centers. Similar insensitivity of Pmax was also observed in low light adapted cultures of Thalassiosira weissflogii (a marine diatom), but not in high light adapted cells where Pmax decreased in proportion to n. This differential sensitivity to decreases in n occurred because $${1 \mathord{\left/ {\vphantom {1 {\tau _{PSII} }}} \right. \kern-\nulldelimiterspace} {\tau _{PSII} }}$$ was close to the maximum achievable rate in the high light adapted cells, whereas $${1 \mathord{\left/ {\vphantom {1 {\tau _{PSII} }}} \right. \kern-\nulldelimiterspace} {\tau _{PSII} }}$$ was initially low in the low light adapted cells and could thus increase in response to decreases in n. Our results indicate that decreases in plant productivity are not necessarily commensurate with photoinhibition, but rather will only occur if decreases in n are sufficient to maximize $${1 \mathord{\left/ {\vphantom {1 {\tau _{PSII} }}} \right. \kern-\nulldelimiterspace} {\tau _{PSII} }}$$ or incident irradiance becomes subsaturating.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Photosynthesis research 48 (1996), S. 395-410 
    ISSN: 1573-5079
    Keywords: chlorophyll fluorescence ; cyclic electron transport ; oxygen evolution ; Photosystem II ; quantum yield
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The oxygen flash yield (YO2) and photochemical yield of PS II (ΦPS II) were simultaneously detected in intact Chlorella cells on a bare platinum oxygen rate electrode. The two yields were measured as a function of background irradiance in the steady-state and following a transition from light to darkness. During steady-state illumination at moderate irradiance levels, YO2 and ΦPS II followed each other, suggesting a close coupling between the oxidation of water and QA reduction (Falkowski et al. (1988) Biochim. Biophys. Acta 933: 432–443). Following a light-to-dark transition, however, the relationship between QA reduction and the fraction of PS II reaction centers capable of evolving O2 became temporarily uncoupled. ΦPS II recovered to the preillumination levels within 5–10 s, while the YO2 required up to 60 s to recover under aerobic conditions. The recovery of YO2 was independent of the redox state of QA, but was accompanied by a 30% increase in the functional absorption cross-section of PS II (σPS II). The hysteresis between YO2 and the reduction of QA during the light-to-dark transition was dependent upon the reduction level of the plastoquinone pool and does not appear to be due to a direct radiative charge back-reaction, but rather is a consequence of a transient cyclic electron flow around PS II. The cycle is engaged in vivo only when the plastoquinone pool is reduced. Hence, the plastoquinone pool can act as a clutch that disconnects the oxygen evolution from photochemical charge separation in PS II.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1573-5079
    Keywords: D1 protein ; photoinhibition ; PS II inhibitors ; Synechococcus PCC 7942
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Light-induced modification of Photosystem II (PS II) complex was characterized in the cyanobacterium Synechococcus sp. PCC 7942 treated with either DCMU (a phenylurea PS II inhibitor) or BNT (a phenolic PS II inhibitor). The irradiance response of photoinactivation of PS II oxygen evolution indicated a BNT-specific photoinhibition that saturated at relatively low intensity of light. This BNT-specific process was slowed down under anaerobiosis, was accompanied by the oxygen-dependent formation of a 39 kDa D1 protein adduct, and was not related to stable QA reduction or the ADRY effect. In the BNT-treated cells, the light-induced, oxygen-independent initial drop of PS II electron flow was not affected by formate, an anion modifying properties of the PS II non-heme iron. For DCMU-treated cells, anaerobiosis did not significantly affect PS II photoinactivation, the D1 adduct was not observed and addition of formate induced similar initial decrease of PS II electron flow as in the BNT-treated cells. Our results indicate that reactive oxygen species (most likely singlet oxygen) and modification of the PS II acceptor side are responsible for the fast BNT-induced photoinactivation of PS II.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Photosynthesis research 24 (1990), S. 89-97 
    ISSN: 1573-5079
    Keywords: chlorophyll a fluorescence ; D1 protein ; oxygen evolving Photosystem II particles ; pheophytin ; photoinactivation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Oxygen evolving Photosystem II particles were exposed for up to 10 h to 100 W m-2 white light at 20°C under aerobic, low oxygen, strictly anaerobic and strongly reducing conditions. The fast and slow photoinactivation processes described earlier (Šetlík et al. 1989) were observed during the first 120 min. The third and by far the slowest process impaired the primary charge separation P680+−Pheo−. Its half-time was about 2.5 h under aerobic and strongly reducing conditions and about 4 h under anaerobic and low oxygen conditions. In these time intervals there were no changes in the chlorophyll-protein and polypeptide composition of the particles irradiated under anaerobic, low oxygen or strongly reducing conditions while a dramatic degradation of chlorophyll-proteins and polypeptides occurred under aerobic conditions.
    Type of Medium: Electronic Resource
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  • 8
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    WILEY-BLACKWELL PUBLISHING
    In:  EPIC3Journal of Phycology, WILEY-BLACKWELL PUBLISHING, ISSN: 0022-3646
    Publication Date: 2018-05-31
    Description: Arctic microalgae experience long periods of continuous darkness during the polar night, where they are unable to photosynthesize. Despite numerous studies on overwintering strategies, such as utilization of stored energy products, formation of resting stages, reduction of metabolic rate and heterotrophic lifestyles, there have been few attempts to assess the in situ physiological state and restoration of the photosynthetic apparatus upon re‐illumination. In this study, we found diverse and active marine phytoplankton communities during the polar night at 78° N. Furthermore, we observed rapid changes (≥20 min) in the efficiency of photosynthetic electron transport upon re‐illumination. High photosynthetic capacity and net primary production were established after 24 h of re‐illumination. Our results suggest that some Arctic autotrophs maintain fully functional photosystem II and downstream electron acceptors during the polar night even though the low in situ net primary production levels measured in January prove that light was not sufficient to support any measurable primary production. Due to low temperatures resulting in low respiratory costs as well as the absence of photo‐damage during the polar night, maintenance of basic photosynthetic machinery may actually pose relatively low metabolic costs for algal cells. This could allow Arctic microalgae to endure the polar night without the formation of dormant stages, enabling them to recover and take advantage of light immediately upon its return during the winter‐spring transition.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
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  • 9
    Publication Date: 2022-10-26
    Description: © The Author(s), 2019. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Inomura, K., Deutsch, C., Wilson, S. T., Masuda, T., Lawrenz, E., Lenka, B., Sobotka, R., Gauglitz, J. M., Saito, M. A., Prášil, O., & Follows, M. J. Quantifying oxygen management and temperature and light dependencies of nitrogen fixation by Crocosphaera watsonii. Msphere, 4(6), (2019): e00531-19, doi: 10.1128/msphere.00531-19.
    Description: Crocosphaera is a major dinitrogen (N2)-fixing microorganism, providing bioavailable nitrogen (N) to marine ecosystems. The N2-fixing enzyme nitrogenase is deactivated by oxygen (O2), which is abundant in marine environments. Using a cellular scale model of Crocosphaera sp. and laboratory data, we quantify the role of three O2 management strategies by Crocosphaera sp.: size adjustment, reduced O2 diffusivity, and respiratory protection. Our model predicts that Crocosphaera cells increase their size under high O2. Using transmission electron microscopy, we show that starch granules and thylakoid membranes are located near the cytoplasmic membranes, forming a barrier for O2. The model indicates a critical role for respiration in protecting the rate of N2 fixation. Moreover, the rise in respiration rates and the decline in ambient O2 with temperature strengthen this mechanism in warmer water, providing a physiological rationale for the observed niche of Crocosphaera at temperatures exceeding 20°C. Our new measurements of the sensitivity to light intensity show that the rate of N2 fixation reaches saturation at a lower light intensity (∼100 μmol m−2 s−1) than photosynthesis and that both are similarly inhibited by light intensities of 〉500 μmol m−2 s−1. This suggests an explanation for the maximum population of Crocosphaera occurring slightly below the ocean surface.
    Description: We thank Stephanie Dutkiewicz and Sallie W. Chisholm for useful discussion, Martin Lukeš for technical assistance for the N2 fixation measurement, and the members of Writing and Communication Center at MIT for their advice on writing. This research was supported by the Japan Student Service Organization (JASSO) (grant L11171020001 to K.I.), the Gordon and Betty Moore Foundation (grant GBMF 3775 to C.D. and grant GBMF 3778 to M.J.F.), the U.S. National Science Foundation (grant OCE-1756524 to S.T.W., grant OCE-1558702 to M.J.F., and grant OCE-PRF 1421196 to J.M.G), the Simons Foundation (Simons Postdoctoral Fellowship in Marine Microbial Ecology award 544338 to K.I., Simons Collaboration on Ocean Processes and Ecology award 329108 to M.J.F., Simons Collaboration on Computational BIOgeochemical Modeling of Marine EcosystemS [CBIOMES] award 549931 to M.J.F.), the Czech Science Foundation (GAČR) (grant 16-15467S to O.P.), and the National Sustainability Programme (NPU) (grant LO1416 Algatech plus to O.P.).
    Keywords: Crocosphaera ; Carbon ; Cell flux model ; Daily cycle ; Iron ; Light ; Nitrogen ; Nitrogen fixation ; Oxygen ; Photosynthesis ; Temperature
    Repository Name: Woods Hole Open Access Server
    Type: Article
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