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  • 1
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Kim, Ju Hyoung; Kim, Kwang Young; Kang, Eun Ju; Lee, Kitack; Kim, Ja-Myung; Park, K T; Shin, Kyoungsoon; Hyun, B; Jeong, Hae Jin (2013): Enhancement of photosynthetic carbon assimilation efficiency by phytoplankton in the future coastal ocean. Biogeosciences, 10(11), 7525-7535, https://doi.org/10.5194/bg-10-7525-2013
    Publication Date: 2024-03-15
    Description: A mesocosm experiment was conducted to evaluate the effects of future climate conditions on photosynthesis and productivity of coastal phytoplankton. Natural phytoplankton assemblages were incubated in field mesocosms under the ambient condition (present condition: ca. 400 ppmv CO2 and ambient temp.), and two future climate conditions (acidification condition: ca. 900 ppmv CO2 and ambient temp.; greenhouse condition: ca. 900 ppmv CO2 and 3 °C warmer than ambient). Photosynthetic parameters of steady-state light responses curves (LCs; measured by PAM fluorometer) and photosynthesis-irradiance curves (P-I curves; estimated by in situ incorporation of 14C) were compared to three conditions during the experiment period. Under acidification, electron transport efficiency (alpha LC) and photosynthetic 14C assimilation efficiency (alpha) were 10% higher than those of the present condition, but maximum rates of relative electron transport (rETRm,LC) and photosynthetic 14C assimilation (PBmax) were lower than the present condition by about 19% and 7%, respectively. In addition, rETRm,LC and alpha LC were not significantly different between and greenhouse conditions, but PBmax and alpha of greenhouse conditions were higher than those of the present condition by about 9% and 30%, respectively. In particular, the greenhouse condition has drastically higher PBmax and alpha than the present condition more than 60% during the post-bloom period. According to these results, two future ocean conditions have major positive effects on the photosynthesis in terms of energy utilization efficiency for organic carbon fixation through the inorganic carbon assimilation. Despite phytoplankton taking an advantage on photosynthesis, primary production of phytoplankton was not stimulated by future conditions. In particular, biomass of phytoplankton was depressed under both acidification and greenhouse conditions after the the pre-bloom period, and more research is required to suggest that some factors such as grazing activity could be important for regulating phytoplankton bloom in the future ocean.
    Keywords: Alkalinity, total; Aragonite saturation state; Bicarbonate ion; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Cell density; Chlorophyll a; Coast and continental shelf; Date; Effective quantum yield; Electron transport rate, relative; Electron transport rate efficiency; Entire community; EXP; Experiment; Field experiment; Figure; Fluorometric; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Geoje_Island; Grazing rate; Grazing rate, standard deviation; Gross community production of carbon dioxide; Gross community production of carbon dioxide, cumulative; Gross community production of carbon dioxide, per chlorophyll a; Gross photosynthesis rate, carbon dioxide, per chlorophyll a; Growth/Morphology; Identification; Incubation duration; Irradiance; Maximal electron transport rate, relative; Maximum potential capacity of photosynthesis; Mesocosm or benthocosm; Nitrate and Nitrite; North Pacific; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; Phosphate; Photosynthetic efficiency, carbon production; Primary production/Photosynthesis; Salinity; Saturation light intensity; Silicate; Species; Table; Temperate; Temperature; Temperature, water; Time of day; Treatment
    Type: Dataset
    Format: text/tab-separated-values, 45219 data points
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  • 2
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Park, K T; Lee, Kitack; Shin, Kyoungsoon; Yang, Eun Jin; Hyun, Bonggil; Kim, Ja-Myung; Noh, Jae Hoon; Kim, Miok; Kong, Bokyung; Choi, Dong Han; Choi, Su-Jin; Jang, Pung-Guk; Jeong, Hae Jin (2014): Direct Linkage between Dimethyl Sulfide Production and Microzooplankton Grazing, Resulting from Prey Composition Change under High Partial Pressure of Carbon Dioxide Conditions. Environmental Science & Technology, 48(9), 4750-4756, https://doi.org/10.1021/es403351h
    Publication Date: 2024-03-15
    Description: Oceanic dimethyl sulfide (DMS) is the enzymatic cleavage product of the algal metabolite dimethylsulfoniopropionate (DMSP) and is the most abundant form of sulfur released into the atmosphere. To investigate the effects of two emerging environmental threats (ocean acidification and warming) on marine DMS production, we performed a large-scale perturbation experiment in a coastal environment. At both ambient temperature and 2 °C warmer, an increase in partial pressure of carbon dioxide (pCO2) in seawater (160-830 ppmv pCO2) favored the growth of large diatoms, which outcompeted other phytoplankton species in a natural phytoplankton assemblage and reduced the growth rate of smaller, DMSP-rich phototrophic dinoflagellates. This decreased the grazing rate of heterotrophic dinoflagellates (ubiquitous micrograzers), resulting in reduced DMS production via grazing activity. Both the magnitude and sign of the effect of pCO2 on possible future oceanic DMS production were strongly linked to pCO2-induced alterations to the phytoplankton community and the cellular DMSP content of the dominant species and its association with micrograzers.
    Keywords: 19-Hexanoyloxyfucoxanthin; Alexandrium sp.; Alkalinity, total; Alloxanthin; Ammonia; Aragonite saturation state; Behaviour; Bicarbonate ion; Biomass; Calcite saturation state; Calculated; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, organic, dissolved; Carbon, organic, particulate; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Cell density; Cerataulina pelagica; Chlorophyll a; Chlorophyll b; Coast and continental shelf; Community composition and diversity; Date; Dimethyl sulfide; Dimethylsulfoniopropionate, particulate; Dimethylsulfoniopropionate lyase activity; Dimethylsulfoniopropionate lyase activity, standard deviation; Entire community; EXP; Experiment; Field experiment; Fucoxanthin; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Grazing rate; Grazing rate, standard error; Identification; Incubation duration; Jangmok; Mesocosm or benthocosm; Nitrate and Nitrite; North Pacific; OA-ICC; Ocean Acidification International Coordination Centre; Other metabolic rates; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; Peridinin; pH; Phosphate; Primary production/Photosynthesis; Salinity; Silicate; Species; Temperate; Temperature; Temperature, water; Treatment; Zeaxanthin
    Type: Dataset
    Format: text/tab-separated-values, 29214 data points
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 79 (1957), S. 1108-1114 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 75 (1994), S. 7526-7530 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: We report on our recent x-ray photoemission spectroscopy investigations of the interface formation of Al with poly(p-phenylene vinylene) (PPV) prepared under various conditions. We have found that during deposition Al reacts with residual hydroxyl groups in the polymer. In addition, we have found that Schottky barrier formation and the associated band bending depend strongly on surface preparation. Samples converted in situ, containing 5% surface oxygen, show band bending that depends on the thickness of the Al overlayer, with effects arising after as little as 1 A(ring) Al. By contrast, a sample converted ex situ, with 10% surface oxygen, is insensitive to aluminum deposition. In view of the results obtained, we feel that surface impurities and adsorbed species may delay Schottky barrier formation by acting as a buffer layer which prevents the PPV substrate from interacting with the growing layer of Al. In the in situ samples where band bending occurs, we find that it takes place after the formation of metallic Al.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 85 (1999), S. 512-517 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: We report on the growth and characterization of beryllium–chalcogenide layers prepared on GaAs (100) by molecular beam epitaxy. Be- and Te-terminated BeTe surfaces show (4×1) and (2×1) reconstructions, respectively. The stability of each surface is investigated by reflection high energy electron diffraction as a function of substrate temperature. The dependence of growth rate of BeTe on growth temperature and Be cell temperature is investigated. The best full width at half maximum (FWHM) of a (400) x-ray rocking curve of BeTe is 78 arcsec. The dependence of the ZnBeSe energy gap on Be composition is obtained by four-crystal x-ray diffraction (XRD) and low temperature photoluminescence measurements. The energy gap of Zn1−xBexSe varies as Eg=0.0107x+2.790 (eV) for small Be composition (x〈0.25) at 77 K. Lattice-matched ZnBeSe (Eg=2.82 eV) and ZnMgBeSe (Eg=2.975 eV) layers show narrower XRD peaks, the FWHM values of which are 64 and 21 arcsec, respectively. The variation of FWHM of x-ray rocking curve due to lattice misfit is investigated for ZnMgBeSe quaternaries with various lattice misfits extending from compressive to tensile strain. The FWHM value under compressive strain increases more steeply with lattice misfit than that under tensile strain. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry 51 (1959), S. 253-256 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0959-8103
    Keywords: poly(p-phenylene-α,α′-diphenyl vinylene) ; poly(p-phenylene-α-phenyl vinylene) ; calcium ; interface ; photoemission spectroscopy ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: We have investigated the interface formation of Ca with poly(p-phenylene α,α′-diphenyl vinylene) (PPV-DP) and poly(p-phenylene α-phenyl vinylene) (PPV-P) using X-ray photoemission spectroscopy (XPS). Similarly to our earlier findings in metal/PPV interface formation, the O 1s peak shifted toward a lower binding energy as soon as Ca was deposited on to the polymers. This was accompanied by the formation of Ca—O, suggesting a chemical origin for the O 1s shift. By contrast, the C 1s peak shift toward a lower binding energy was observed relatively later, after about 4 Å of Ca deposition. At the same time, a new C 1s component became noticable at about -1.5 eV relative to the initial C 1s peak. This component signifies the possibility of polymer disruption by the Ca atoms to form Ca—C species. The C 1s peak shift is attributed to Ca induced surface band bending and barrier formation as in the case of metal/PPV interface formation. The disruption of the polymer may also induce changes in the interface electronic states and contribute to the C 1s peak shift. From the intensity attenuation analysis, we conclude that the initial 15 Å of Ca overlayer is contaminated by the Ca—O and Ca—C species and the overlayer is pure beyond 15 Å of Ca coverage.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 23 (1995), S. 89-98 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: We report on our recent x-ray photoemission spectroscopy investigations of the interface formation of metals with poly(p-phenylene vinylene) (PPV) prepared under various conditions. We have found that during deposition the metal reacts with residual hydroxyl groups in the polymer. In addition, we have found that Schottky barrier formation and the associated band bending depend strongly on surface preparation. In the case of Al deposition, samples converted in situ, containing 5% surface oxygen, show band bending that depends on the thickness of the metal overlayer, with effects arising after as little as 1 Å of metal. On the other hand, a sample converted ex situ, with 10% surface oxygen, is insensitive to aluminium deposition. We feel that surface impurities and adsorbed species may delay Schottky barrier formation by acting as a buffer layer that prevents the PPV substrate from interacting with the growing layer of Al. By contrast, the Ca/PPV surface exhibits delayed band bending, with strong interactions between surface oxygen and Ca. Our results indicate that band bending at the metal/PPV interface is governed by the metallicity of the metal overlayer, which itself is influenced by the interface reaction of the deposited metal with the PPV substrate or the surface residual impurities. Finally, the degree of band bending observed did not correlate directly with the differences in work functions between the metals and PPV.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Publication Date: 2004-11-01
    Print ISSN: 1359-6462
    Electronic ISSN: 1872-8456
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Published by Elsevier
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  • 10
    Publication Date: 1957-03-01
    Print ISSN: 0002-7863
    Electronic ISSN: 1520-5126
    Topics: Chemistry and Pharmacology
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