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An engineer looks at photosynthesis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bbpc.19800841026openalex-snapshot
Stoichiometry of Proton Translocation during Photosynthesis
inferredcites →https://doi.org/10.1002/bit.260070209openalex-snapshot
The motion of algae in turbulent flow
inferredcites →https://doi.org/10.1002/bit.260250802openalex-snapshot
Maximum photosynthetic efficiency: A problem to be resolved
inferredcites →https://doi.org/10.1002/j.2326-1951.1982.tb02101.xopenalex-snapshot
Sunlight, Earth Life
inferredcites →https://doi.org/10.1002/jctb.503300105openalex-snapshot
The photosynthetic efficiency of Chlorella biomass growth with reference to solar energy utilisation
inferredcites →https://doi.org/10.1007/978-3-642-94798-8_30openalex-snapshot
The path of carbon in photosynthesis
inferredcites →https://doi.org/10.1007/bf00388218openalex-snapshot
O2-dependent inhibition of photosynthetic capacity in intact isolated chloroplasts and isolated cells from spinach leaves illuminated in the absence of CO2
inferredcites →https://doi.org/10.1007/bf00388894openalex-snapshot
Rates of synthesis and source of glycolate in intact chloroplasts
inferredcites →https://doi.org/10.1007/bf00389050openalex-snapshot
Regulation of photosynthetic electron transport and photophosphorylation in intact chloroplasts and leaves of Spinacia oleracea L.
inferredcites →https://doi.org/10.1007/bf00390153openalex-snapshot
Effects of oxygen on the electron transport chain of photosynthesis
inferredcites →https://doi.org/10.1007/bf00390681openalex-snapshot
Phytoplankton photosynthetic response to vertical movement in a mixed layer
inferredcites →https://doi.org/10.1016/0003-9861(51)90082-3openalex-snapshot
Studies on reactions of illuminated chloroplasts
inferredcites →https://doi.org/10.1016/0003-9861(63)90547-2openalex-snapshot
Photosynthesis and respiration
inferredcites →https://doi.org/10.1016/0003-9861(79)90052-3openalex-snapshot
Models describing the kinetics of ribulose biphosphate carboxylase-oxygenase
inferredcites →https://doi.org/10.1016/0005-2728(67)90091-6openalex-snapshot
The kinetics of the pH rise in illuminated chloroplast suspensions
inferredcites →https://doi.org/10.1016/0005-2728(68)90124-2openalex-snapshot
The stoichiometric relation of phosphorylation to electron transport in isolated chloroplasts
inferredcites →https://doi.org/10.1016/0005-2728(70)90046-0openalex-snapshot
Photoreduction of 2,6-dichlorophenolindophenol by chloroplasts with exogenous Mn2+ as electron donor
inferredcites →https://doi.org/10.1016/0005-2728(71)90159-9openalex-snapshot
Localization of photophosphorylation and proton transport activities in various regions of the chloroplast lamellae
inferredcites →https://doi.org/10.1016/0005-2728(71)90205-2openalex-snapshot
The relationship between Q, C-550 and cytochrome b 559 in photoreactions at −196° in chloroplasts
inferredcites →https://doi.org/10.1016/0005-2728(73)90163-1openalex-snapshot
Optical and kinetic properties of semireduced plastoquinone and ubiquinone: Electron acceptors in photosynthesis
inferredcites →https://doi.org/10.1016/0005-2728(74)90067-xopenalex-snapshot
The electric generator in the photosynthesis of green plants. II. Kinetic correlation between protolytic reactions and redox reactions
inferredcites →https://doi.org/10.1016/0005-2728(74)90068-1openalex-snapshot
Proton evolution associated with the photooxidation of water in photosynthesis
inferredcites →https://doi.org/10.1016/0005-2728(74)90135-2openalex-snapshot
Studies on the energy coupling sites of photophosphorylation IV. The relation of proton fluxes to the electron transport and ATP formation associated with Photosystem II
inferredcites →https://doi.org/10.1016/0005-2728(75)90128-0openalex-snapshot
Reduction of oxygen by the electron transport chain of chloroplasts during assimilation of carbon dioxide
inferredcites →https://doi.org/10.1016/0005-2728(76)90119-5openalex-snapshot
Factors affecting the ADP/O ratio in isolated chloroplasts
inferredcites →https://doi.org/10.1016/0005-2728(76)90174-2openalex-snapshot
Relations between the electrical potential, pH gradient, proton flux and phosphorylation in the photosynthetic membrane
inferredcites →https://doi.org/10.1016/0005-2728(76)90204-8openalex-snapshot
Determination of H+e− ratios in chloroplasts with flashing light
inferredcites →https://doi.org/10.1016/0005-2728(79)90016-1openalex-snapshot
Redox titration of electron acceptor Q and the plastoquinone pool in Photosystem II
inferredcites →https://doi.org/10.1016/0005-2728(79)90136-1openalex-snapshot
Isotope ratios in photosynthetic oxygen
inferredcites →https://doi.org/10.1016/0005-2728(80)90011-0openalex-snapshot
Inhibition of Photosystem II by formate. Possible evidence for a direct role of bicarbonate in photosynthetic oxygen evolution
inferredcites →https://doi.org/10.1016/0005-2728(80)90100-0openalex-snapshot
Observation of two quenchers of chlorophyll fluorescence in chloroplasts at −196°C
inferredcites →https://doi.org/10.1016/0005-2728(83)90115-9openalex-snapshot
Oxygen-evolution patterns from spinach Photosystem II preparations
inferredcites →https://doi.org/10.1016/0006-291x(76)91127-xopenalex-snapshot
Light induced activation of fructose-1,6-bisphosphatase in isolated intact chloroplasts
inferredcites →https://doi.org/10.1016/0006-3002(49)90136-5openalex-snapshot
On the interrelation of respiration and photosynthesis in green plants
inferredcites →https://doi.org/10.1016/0006-3002(56)90003-8openalex-snapshot
On the inhibition of photosynthesis by intense light
inferredcites →https://doi.org/10.1016/0006-3002(56)90412-7openalex-snapshot
Reversible changes in bacteriochlorophyll in purple bacteria upon illumination
inferredcites →https://doi.org/10.1016/0006-3002(61)90050-6openalex-snapshot
Partial purification and determination of oxidation reduction potential of the photosynthetic chlorophyll complex absorbing at 700 mμ
inferredcites →https://doi.org/10.1016/0006-3002(62)90825-9openalex-snapshot
Thyroxine-binding properties of bovine M-2 glycoprotein
inferredcites →https://doi.org/10.1016/0014-5793(74)81018-5openalex-snapshot
On the reduction of chlorophyll‐AI in the presence of the plastoquinone antagonist dibromothymoquinone
inferredcites →https://doi.org/10.1016/0014-5793(75)80038-xopenalex-snapshot
The pH indicator phenol red as an artificial electron acceptor in spinach chloroplasts
inferredcites →https://doi.org/10.1016/0014-5793(75)80399-1openalex-snapshot
Neutral red, a rapid indicator for pH‐changes in the inner phase of thylakoids
inferredcites →https://doi.org/10.1016/0014-5793(79)80396-8openalex-snapshot
Preparation of an active, oxygen‐evolving photosystem 2 particle from a blue—green alga
inferredcites →https://doi.org/10.1016/0014-5793(80)80022-6openalex-snapshot
Isotopic composition of photosynthetic O2 flash yields in the presence of H218O and HC18O−3
inferredcites →https://doi.org/10.1016/0014-5793(80)80390-5openalex-snapshot
Flash‐induced redox changes of P700 and plastocyanin in chloroplasts suspended in fluid media at sub‐zero temperatures
inferredcites →https://doi.org/10.1016/0014-5793(80)80527-8openalex-snapshot
An EPR analysis of the partially purified cytochrome bf complex of higher‐plant chloroplasts
inferredcites →https://doi.org/10.1016/0014-5793(80)81159-8openalex-snapshot
Electron and proton transfer events in chloroplasts during a short series of flashes
inferredcites →https://doi.org/10.1016/0014-5793(81)80295-5openalex-snapshot
Measurement of the midpoint potential of the pheophytin acceptor of photosystem II
inferredcites →https://doi.org/10.1016/0014-5793(81)80520-0openalex-snapshot
Release of polypeptides from highly active O2‐evolving photosystem‐2 preparation by this treatment
inferredcites →https://doi.org/10.1016/0014-5793(81)80595-9openalex-snapshot
A rapid method for extraction of oxygen‐evolving photosystem 2 preparations from cyanobacteria
inferredcites →https://doi.org/10.1016/0014-5793(82)80578-4openalex-snapshot
Patterns of oxygen emission from active oxygen‐evolving photosystem II particles subjected to sequences of flashes
inferredcites →https://doi.org/10.1016/0022-0981(78)90096-5openalex-snapshot
Photosynthèse phytoplanctonique: Réponse à un stimulus simple, imitant les variations rapides de la lumière engendrées par les vagues
inferredcites →https://doi.org/10.1016/0022-5193(75)90148-4openalex-snapshot
Water decomposition in photosynthesis? A critical reconsideration
inferredcites →https://doi.org/10.1016/0022-5193(76)90124-7openalex-snapshot
Possible molecular mechanisms of the protonmotive function of cytochrome systems
inferredcites →https://doi.org/10.1016/0304-4173(79)90008-9openalex-snapshot
Energy conversion in the functional membrane of photosynthesis. Analysis by light pulse and electric pulse methods
inferredcites →https://doi.org/10.1016/0926-6585(65)90207-4openalex-snapshot
Cinétiques des réactions liées a l'émission d'oxygène photosynthétique
inferredcites →https://doi.org/10.1016/b978-0-12-152814-0.50005-8openalex-snapshot
Regulation of Enzymes in C4 Photosynthesis
inferredcites →https://doi.org/10.1016/b978-0-444-89608-7.50001-0openalex-snapshot
Topics in Photosynthesis
inferredcites →https://doi.org/10.1016/c2013-0-12206-4openalex-snapshot
Primary Processes in Photosynthesis
inferredcites →https://doi.org/10.1016/s0021-9258(17)40199-2openalex-snapshot
Subunit Structure of Chloroplast Photosystem I Reaction Center
inferredcites →https://doi.org/10.1016/s0021-9258(18)62215-xopenalex-snapshot
Electron Transport and Photophosphorylation in Chloroplasts as a Function of the Electron Acceptor
inferredcites →https://doi.org/10.1016/s0021-9258(19)42246-1openalex-snapshot
Effects of Adenine Nucleotides and of Photophosphorylation on H+ Uptake and the Magnitude of the H+ Gradient in Illuminated Chloroplasts
inferredcites →https://doi.org/10.1016/s0021-9258(19)45111-9openalex-snapshot
Partial Resolution of the Enzymes Catalyzing Photophosphorylation
inferredcites →https://doi.org/10.1016/s0031-9422(00)90901-4openalex-snapshot
Biochemistry of Chloroplasts
inferredcites →https://doi.org/10.1017/s0033583500000834openalex-snapshot
Coupling of quanta, electrons, fields, ions and phosphorylation in the functional membrane of photosynthesis. Results by pulse spectroscopic methods
inferredcites →https://doi.org/10.1021/j150414a003openalex-snapshot
Photosynthesis in Flashing Light.
inferredcites →https://doi.org/10.1021/j150427a001openalex-snapshot
Flash Saturation and Reaction Periods in Photosynthesis.
inferredcites →https://doi.org/10.1021/ja01650a097openalex-snapshot
LIGHT INDUCED PHOSPHORYLATION BY CELL-FREE PREPARATIONS OF PHOTOSYNTHETIC BACTERIA1
inferredcites →https://doi.org/10.1021/ja01848a512openalex-snapshot
Heavy Oxygen (O18) as a Tracer in the Study of Photosynthesis
inferredcites →https://doi.org/10.1038/172975a0openalex-snapshot
Mechanism of Phosphorylation in the Respiratory Chain
inferredcites →https://doi.org/10.1038/186136a0openalex-snapshot
Function of the Two Cytochrome Components in Chloroplasts: A Working Hypothesis
inferredcites →https://doi.org/10.1038/186533a0openalex-snapshot
A New Copper Protein from Chlorella Ellipsoidea
inferredcites →https://doi.org/10.1038/191144a0openalex-snapshot
Coupling of Phosphorylation to Electron and Hydrogen Transfer by a Chemi-Osmotic type of Mechanism
inferredcites →https://doi.org/10.1038/219915a0openalex-snapshot
Light Induced Proton Gradient links Electron Transport and Phosphorylation
inferredcites →https://doi.org/10.1038/272319a0openalex-snapshot
X-ray crystal structure analysis of plastocyanin at 2.7 Å resolution
inferredcites →https://doi.org/10.1042/bj1010103openalex-snapshot
Photosynthesis by sugar-cane leaves. A new carboxylation reaction and the pathway of sugar formation
inferredcites →https://doi.org/10.1042/bj1090527openalex-snapshot
Photosynthetic control by isolated pea chloroplasts
inferredcites →https://doi.org/10.1073/pnas.51.6.1244openalex-snapshot
DAMPED SINUSOIDAL OSCILLATIONS OF CYTOPLASMIC REDUCED PYRIDINE NUCLEOTIDE IN YEAST CELLS
inferredcites →https://doi.org/10.1073/pnas.55.1.170openalex-snapshot
ATP formation caused by acid-base transition of spinach chloroplasts.
inferredcites →https://doi.org/10.1073/pnas.57.2.439openalex-snapshot
THE AMINO ACID SEQUENCE OF SPINACH FERREDOXIN
inferredcites →https://doi.org/10.1073/pnas.68.5.1010openalex-snapshot
A New Photosynthetic Pigment, “P430”: Its Possible Role as the Primary Electron Acceptor of Photosystem I
inferredcites →https://doi.org/10.1073/pnas.74.8.3377openalex-snapshot
Quantum efficiency of photosynthetic energy conversion.
inferredcites →https://doi.org/10.1073/pnas.75.12.6031openalex-snapshot
A third site of porton translocation in green plant photosynthetic electron transport
inferredcites →https://doi.org/10.1073/pnas.77.8.4712openalex-snapshot
Stoichiometry of system I and system II reaction centers and of plastoquinone in different photosynthetic membranes
inferredcites →https://doi.org/10.1073/pnas.78.5.2942openalex-snapshot
Proton transport in photooxidation of water: A new perspective on photosynthesis
inferredcites →https://doi.org/10.1085/jgp.15.4.391openalex-snapshot
A SEPARATION OF THE REACTIONS IN PHOTOSYNTHESIS BY MEANS OF INTERMITTENT LIGHT
inferredcites →https://doi.org/10.1085/jgp.16.2.191openalex-snapshot
THE PHOTOCHEMICAL REACTION IN PHOTOSYNTHESIS
inferredcites →https://doi.org/10.1085/jgp.36.4.563openalex-snapshot
TIME COURSE AND QUANTUM EFFICIENCY OF PHOTOSYNTHESIS IN CHLORELLA
inferredcites →https://doi.org/10.1086/405228openalex-snapshot
Les Oestrogenes Naturels: Biosynthese et Metabolisme.Lise Cedard
inferredcites →https://doi.org/10.1093/aibsbulletin/3.5.11openalex-snapshot
Algal Culture from Laboratory to Pilot Plant
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a076199openalex-snapshot
Formation of Hydrogen Peroxide and Oxygen Dependence of Photosynthetic CO2 Assimilation by Intact Chloroplasts
inferredcites →https://doi.org/10.1093/plankt/4.2.313openalex-snapshot
Effets des fluctuations rapides de la lumière sur la photosynthèse du phytoplancton
inferredcites →https://doi.org/10.1104/pp.29.2.152openalex-snapshot
Growth Rate of Chlorella in Flashing Light.
inferredcites →https://doi.org/10.1104/pp.35.4.477openalex-snapshot
Red Drop and Role of Auxiliary Pigments in Photosynthesis
inferredcites →https://doi.org/10.1104/pp.40.2.209openalex-snapshot
Carbon Dioxide Fixation in Sugarcane Leaves
inferredcites →https://doi.org/10.1104/pp.51.1.104openalex-snapshot
Photosynthetic Production of Hydrogen Peroxide by Anacystis nidulans
inferredcites →https://doi.org/10.1104/pp.56.1.72openalex-snapshot
H2 Metabolism in Photosynthetic Organisms
inferredcites →https://doi.org/10.1104/pp.64.4.656openalex-snapshot
Photosynthetic Oxygen Reduction in Isolated Intact Chloroplasts and Cells in Spinach
inferredcites →https://doi.org/10.1111/j.1399-3054.1961.tb07916.xopenalex-snapshot
Induction Phenomena in Photosynthesis of Algae
inferredcites →https://doi.org/10.1111/j.1432-1033.1970.tb00326.xopenalex-snapshot
The Necessity of an Electric Potential Difference and its Use for Photophosphorylation in Short Flash Groups
inferredcites →https://doi.org/10.1111/j.1432-1033.1979.tb12981.xopenalex-snapshot
Light‐Induced Proton Transport by Chloroplasts Suspended in Fluid Media at Sub‐Zero Temperatures: Kinetics and Stoichiometry
inferredcites →https://doi.org/10.1111/j.1469-185x.1966.tb01501.xopenalex-snapshot
CHEMIOSMOTIC COUPLING IN OXIDATIVE AND PHOTOSYNTHETIC PHOSPHORYLATION
inferredcites →https://doi.org/10.1111/j.1469-8137.1972.tb04069.xopenalex-snapshot
ENDOGENOUS INORGANIC CARBON SOURCES IN PLANT PHOTOSYNTHESIS
inferredcites →https://doi.org/10.1111/j.1469-8137.1973.tb02027.xopenalex-snapshot
PHOTOSYNTHETIC INDUCTION PHENOMENA AND THE LIGHT ACTIVATION OF RIBULOSE DIPHOSPHATE CARBOXYLASE
inferredcites →https://doi.org/10.1111/j.1751-1097.1962.tb08111.xopenalex-snapshot
Progress in Photobiology
inferredcites →https://doi.org/10.1111/j.1751-1097.1969.tb05696.xopenalex-snapshot
UN NOUVEAU MODELE DES CENTRES PHOTOCHIMIQUES DU SYSTEME II*
inferredcites →https://doi.org/10.1111/j.1751-1097.1970.tb06017.xopenalex-snapshot
COOPERATION OF CHARGES IN PHOTOSYNTHETIC O 2 EVOLUTION–I. A LINEAR FOUR STEP MECHANISM
inferredcites →https://doi.org/10.1111/j.1751-1097.1971.tb06174.xopenalex-snapshot
STUDIES OF SYSTEM II PHOTOCENTERS BY COMPARATIVE MEASUREMENTS OF LUMINESCENCE, FLUORESCENCE, AND OXYGEN EMISSION*
inferredcites →https://doi.org/10.1111/j.1751-1097.1971.tb06175.xopenalex-snapshot
COOPERATION OF CHARGES IN PHOTOSYNTHETIC O 2 EVOLUTION‐II. DAMPING OF FLASH YIELD OSCILLATION, DEACTIVATION*
inferredcites →https://doi.org/10.1111/j.1751-1097.1971.tb06177.xopenalex-snapshot
CHLOROPHYLL‐PROTEINS AND REACTION CENTER PREPARATIONS FROM PHOTOSYNTHETIC BACTERIA, ALGAE AND HIGHER PLANTS*,‡
inferredcites →https://doi.org/10.1111/j.1751-1097.1981.tb09078.xopenalex-snapshot
THE ACCEPTOR SIDE OF PHOTOSYSTEM II IN PHOTOSYNTHESIS
inferredcites →https://doi.org/10.1126/science.120.3113.353openalex-snapshot
Reversible Changes in the Absorption Spectrum of Chlorella upon Irradiation
inferredcites →https://doi.org/10.1126/science.132.3423.355openalex-snapshot
Two Forms of Chlorophyll a in vivo with Distinct Photochemical Functions
inferredcites →https://doi.org/10.1146/annurev.bi.33.070164.000245openalex-snapshot
Prefatory Chapter
inferredcites →https://doi.org/10.1146/annurev.pp.09.060158.000245openalex-snapshot
The Quantum Yield of Photosynthesis
inferredcites →https://doi.org/10.1146/annurev.pp.13.060162.000331openalex-snapshot
Structure and Chemistry of Plastids
inferredcites →https://doi.org/10.1146/annurev.pp.22.060171.002345openalex-snapshot
The Relation of Ion Transport to Phosphorylation
inferredcites →https://doi.org/10.1146/annurev.pp.25.060174.002141openalex-snapshot
Metabolite Exchange Between Chloroplasts and Cytoplasm
inferredcites →https://doi.org/10.1146/annurev.pp.30.060179.000455openalex-snapshot
Roles of a Coupling Factor for Photophosphorylation in Chloroplasts
inferredcites →https://doi.org/10.1146/annurev.pp.33.060182.000411openalex-snapshot
Blue Light Effects on Respiration
inferredcites →https://doi.org/10.1515/znb-1968-0222openalex-snapshot
On the ion transport system of photosynthesis — Investigations on a molecular level —
inferredcites →https://doi.org/10.1515/znb-1968-1203openalex-snapshot
Correlation between Field Formation, Proton Translocation, and the Light Reactions in Photosynthesis
inferredcites →https://doi.org/10.2307/2257613openalex-snapshot
Physiology and Biochemistry of Algae.
inferredcites →https://doi.org/10.4319/lo.1968.13.4.0697openalex-snapshot
LIGHT FIELD FLUCTUATIONS IN THE PHOTIC ZONE1
inferredcites →https://doi.org/10.4319/lo.1983.28.4.0688openalex-snapshot
Photosynthesis of natural phytoplankton under high frequency light fluctuations simulating those induced by sea surface waves1
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4810070openalex-extracted
Mathematical Model to Simulate Dynamics of Photosynthetic Light Reactions in an Oscillating Light
inferred← citeshttps://doi.org/10.1002/(sici)1097-0290(19980920)59:6<705::aid-bit7>3.0.co;2-jopenalex-snapshot
Light/dark cycles in the growth of the red microalgaPorphyridium sp.
inferred← citeshttps://doi.org/10.1002/bit.22676openalex-snapshot
The oxygen evolution methodology affects photosynthetic rate measurements of microalgae in well‐defined light regimes
inferred← citeshttps://doi.org/10.1007/978-1-4612-1392-5_34openalex-snapshot
Effect of Light/Dark Cycle on Bacterial Hydrogen Production by Rhodobacter sphaeroides RV
inferred← citeshttps://doi.org/10.1007/978-94-009-2823-7_11openalex-snapshot
Measurement and Analysis of Chlorophyll Fluorescence in Plants Using Modulated Actinic Illumination
inferred← citeshttps://doi.org/10.1007/s004490050308openalex-snapshot
Effects of culture temperature shift and light-dark time cycle on the cellular sugar accumulation of Chlorella pyrenoidosa
inferred← citeshttps://doi.org/10.1016/0168-1656(86)90041-6openalex-snapshot
Frequency response analysis of oxygen evolution by algae
inferred← citeshttps://doi.org/10.1016/0922-338x(94)90296-8openalex-snapshot
Effect of culture temperature shift on the cellular sugar accumulation of Chlorella vulgaris SO-26
inferred← citeshttps://doi.org/10.1016/b978-0-08-088504-9.00103-3openalex-snapshot
Photobioreactors – Models of Photosynthesis and Related Effects
inferred← citeshttps://doi.org/10.1016/b978-0-444-64046-8.00081-1openalex-snapshot
Photobioreactors – Models of Photosynthesis and Related Effects
inferred← citeshttps://doi.org/10.1016/j.biortech.2016.12.021openalex-snapshot
Effect of light-dark cycles on hydrogen and poly-β-hydroxybutyrate production by a photoheterotrophic culture and Rhodobacter capsulatus using a dark fermentation effluent as substrate
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109138openalex-snapshot
A mathematical model to simulate the dynamics of photosynthetic light reactions under harmonically oscillating light
inferred← citeshttps://doi.org/10.1016/s0009-2509(01)00048-3openalex-snapshot
A model integrating fluid dynamics in photosynthesis and photoinhibition processes
inferred← citeshttps://doi.org/10.1023/a:1023879619535openalex-snapshot
Modeling of photobioreactors: Application to bubble column simulation
inferred← citeshttps://doi.org/10.1111/ppl.70421openalex-snapshot
Constitutive and Regulatory Responses of Arabidopsis thaliana to Harmonically Oscillating Light
inferred← citeshttps://doi.org/10.1385/abab:84-86:1-9:431openalex-snapshot
Effect of Light/Dark Cycle on Bacterial Hydrogen Production by Rhodobacter sphaeroides RV
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publishing outside journals, and publishes on CiteStamp rails. Submission is free
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