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  1. 1961
    “…This experimental study using unialgal cultures revealed that both O. smithii and O. itoi utilize only the efficient violaxanthin cycle for photoprotection as a dissipation system of surplus energy under prolonged high-light stress, although they possess chlorophyll c with diadinoxanthin.…”
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    Utilizing the Effective Xanthophyll Cycle for Blooming of Ochromonas smithii and O. itoi (Chrysophyceae) on the Snow Surface
  2. 1962
    “…Chloroplast thylakoid membranes isolated from a CSK T-DNA insertion mutant and from wild-type Arabidopsis thaliana exhibit similar light- and redox-induced (32)P-labelling of LHC II and changes in 77 K chlorophyll fluorescence emission spectra, while room-temperature chlorophyll fluorescence emission transients from Arabidopsis leaves are perturbed by inactivation of CSK. …”
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    Discrete Redox Signaling Pathways Regulate Photosynthetic Light-Harvesting and Chloroplast Gene Transcription
  3. 1963
    “…As an alternative, chlorophyll meter readings and N-NO(3) concentration determination in petiole sap were proposed, but these assays are not always satisfactory. …”
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    Nitrogen Concentration Estimation in Tomato Leaves by VIS-NIR Non-Destructive Spectroscopy
  4. 1964
    “…When photosystem II (PSII) is exposed to excess light, singlet oxygen ((1)O(2)) formed by the interaction of molecular oxygen with triplet chlorophyll. Triplet chlorophyll is formed by the charge recombination of triplet radical pair (3)[P680(•+)Pheo(•−)] in the acceptor-side photoinhibition of PSII. …”
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    Evidence on the Formation of Singlet Oxygen in the Donor Side Photoinhibition of Photosystem II: EPR Spin-Trapping Study
  5. 1965
    “…Primary productivity, in terms of chlorophyll-a concentration and net primary production was affected by ecological but not evolutionary factors. …”
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    Ecological and Evolutionary Effects of Stickleback on Community Structure
  6. 1966
    “…The net photosynthetic rate (P (N)), chlorophyll fluorescence parameters, antioxidant substances, antioxidant enzymes, photosystem 1 (PS1) and PS2 activities were studied through methyl viologen (MV) treatment. …”
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    Photooxidation Tolerance Characters of a New Purple Pepper
  7. 1967
    “…CASas plants also had a lower CO(2) assimilation rate that was attributed to a lower photosynthetic electron transport rate, leading to higher chlorophyll fluorescence. Gene co-expression combined with analyses of chlorophyll content and transcription levels of photosynthesis-related genes indicate that CAS is involved in the formation of the photosynthetic electron transport system. …”
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    Regulation of the calcium-sensing receptor in both stomatal movement and photosynthetic electron transport is crucial for water use efficiency and drought tolerance in Arabidopsis
  8. 1968
    “…The photosynthesis, relative chlorophyll content,differentially expressed genes (DEGs) and differentially expressed proteins (DEPs) of L. confusa that cultivated in calcareous and sandstone soils were investigated. …”
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    Characterization and Molecular Interpretation of the Photosynthetic Traits of Lonicera confusa in Karst Environment
  9. 1969
    “…In addition, across both seasons the invasive has the advantage over the native with higher chlorophyll/carotenoids and chlorophyll a/b ratios, percent N, and leaf protein. …”
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    Stress Tolerance and Ecophysiological Ability of an Invader and a Native Species in a Seasonally Dry Tropical Forest
  10. 1970
    “…Physiological studies were conducted through analysis of relative water content (RWC), photosynthetic pigments, chlorophyll a fluorescence, and malate content. No changes in RWC were observed among treatments; however, significant decreases in chlorophyll a content and photosynthetic parameters, including optimal irradiance (I (opt)) and maximum electron transport rate (ETR(max)), were determined by rapid light curves (RLC). …”
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    The Epiphytic Fern Elaphoglossum luridum (Fée) Christ. (Dryopteridaceae) from Central and South America: Morphological and Physiological Responses to Water Stress
  11. 1971
    “…(Yamauchi and Kimura, 2011) We demonstrate that regulating photochemical energy transfer in heat-treated wheat at 40 °C with light contributed to heat tolerance of the photosystem. Chlorophyll fluorescence analysis using heat-stressed wheat seedlings in light showed increased non-photochemical quenching (NPQ) of chlorophyll fluorescence, which was due to thermal dissipation that was increased by state 1 to state 2 transition. …”
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    Regulation of Photochemical Energy Transfer Accompanied by Structural Changes in Thylakoid Membranes of Heat-Stressed Wheat
  12. 1972
    “…In the test seedlings, the root-shoot elongation, biomass production, and the chlorophyll content were significantly decreased with increasing NaCl concentrations. …”
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    Physiochemical Studies of Sodium Chloride on Mungbean (Vigna radiata L. Wilczek) and Its Possible Recovery with Spermine and Gibberellic Acid
  13. 1973
    “…Ag slowly accumulated in the exposed periphyton, which decreased periphyton carbon and chlorophyll a content and increased periphyton C:P and N:P in the carbon rich lakes. …”
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    Phosphorus Availability Alters the Effects of Silver Nanoparticles on Periphyton Growth and Stoichiometry
  14. 1974
    “…The water content of the sediments, total organic matters and chlorophyll a values were determined, and sediment samples were subjected to granulometric analysis. …”
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    Population fluctuation and vertical distribution of meiofauna in the Red Sea interstitial environment
  15. 1975
    “…Physiological and metabolite measurements indicated that the photosynthetic capacity and chlorophyll content of the cells decreased, while neutral lipids increased in N-deprived cultures. …”
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    Whole-cell response to nitrogen deprivation in the diatom Phaeodactylum tricornutum
  16. 1976
    por Abinandan, S., Shanthakumar, S.
    Publicado 2016
    “…The experimental results were statistically significant with R (2) value of 0.9527 and 0.960 for CO(2) removal and accumulation of chlorophyll content, respectively. Among the various interactions, interactive effects between the parameters pH and inoculum size was statistically significant (P < 0.05) for CO(2) removal and chlorophyll accumulation. …”
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    Evaluation of photosynthetic efficacy and CO(2) removal of microalgae grown in an enriched bicarbonate medium
  17. 1977
    “…This study attempts to evaluate the extent of As resistance, chlorophyll content, and metabolic changes in As-polluted (5, 10, 15, and 20 mg L(−1) As) B. nivea in hydroponics. …”
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    Biochemical and Metabolic Changes in Arsenic Contaminated Boehmeria nivea L.
  18. 1978
    “…Soluble sugar, total sugar, glucose, sucrose, fructose, starch, chlorophyll a, b, ab, carotenoid, anthocyanin, lipase, α‐amylase, and protease were measured every 2 weeks up to sprouting time. …”
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    Change in carbohydrate and enzymes from harvest to sprouting in garlic
  19. 1979
    “…The difference in the spatiotemporal response of chlorophyll is due to the southward advection of Leeuwin current during these events. …”
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    Changes in biological productivity associated with Ningaloo Niño/Niña events in the southern subtropical Indian Oceanin recent decades
  20. 1980
    “…We investigated the electrical conductivity (EC), total chlorophyll concentration (Chl), nutrient stoichiometry and chlorophyll fluorescence signals in a subtropical montane cloud forest in south-west China. …”
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    Physiological Responses of Two Epiphytic Bryophytes to Nitrogen, Phosphorus and Sulfur Addition in a Subtropical Montane Cloud Forest
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