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  • 1
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Sultana, Rumana; Casareto, Beatriz E; Sohrin, Rumi; Suzuki, Toshiyuki; Alam, Md Shafiul; Fujimura, Hiroyuki; Suzuki, Yoshimi (2016): Response of Subtropical Coastal Sediment Systems of Okinawa, Japan, to Experimental Warming and High pCO2. Frontiers in Marine Science, 3, https://doi.org/10.3389/fmars.2016.00100
    Publication Date: 2024-03-15
    Description: Increasing seawater temperatures and CO2 levels associated with climate change affect the shallow marine ecosystem function. In this study, the effects of elevated seawater temperature and partial pressure of CO2 (pCO2) on subtropical sediment systems of mangrove, seagrass, and coral reef lagoon habitats of Okinawa, Japan, were examined. Sediment and seawater from each habitat were exposed to four pCO2-temperature treatments, including ambient pCO2- ambient temperature, ambient pCO2-high temperature (ambient temperature + 4°C), high pCO2 (936 ppm)-ambient temperature, and high pCO2-high temperature. Parameters including primary production, nutrient flux, pigment content, photosynthetic community composition, and bacterial abundance were examined. Neither high temperature nor high pCO2 alone impacted mangrove and seagrass sediment primary production significantly (Tukey's test, P 〉 0.05). However, the combined stress significantly (Tukey's test, P 〈 0.01) increased primary production in these two habitats. In sediments from the coral reef lagoon, single and combined stress treatments induced a shift from heterotrophy to autotrophy. Significant increases in net primary production (Tukey's test, P 〈 0.01), and gross primary production (Tukey's test, P 〈 0.05) under the combined stress suggested that benthic microalgae in mangrove and seagrass sediments were more responsive to high temperature and pCO2 conditions than those in coral reef lagoon sediments. Additionally, combined stress significantly increased the sediment chlorophyll a content (Tukey's test, P 〈 0.05) in all habitats. These increases were associated with increased net primary production, indicating that combined stress stimulates primary production activity by the photosynthetic benthic microalgae in all habitats. Diatom activity increased, as silicate uptake increased in all habitats. Microbial abundance significantly increased under the combined stress treatment (Tukey's test, P 〈 0.01), but did not exceed autotrophic activity. Respiration did not change significantly in any of the three habitats (Tukey's test, P 〉 0.05) under the combined stress, suggesting that heterotrophic processes were less affected by the combined stress than autotrophic processes. In summary, mangrove and seagrass sediments minimize the negative impacts of elevated temperature and pCO2 via increased primary production and carbon storage. Lagoonal sediments also act as a carbon sink under temperature and ocean acidification stress.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Ammonium, flux; Ammonium, flux, standard deviation; Aragonite saturation state; Benthos; beta-Carotene, flux; beta-Carotene, flux, standard deviation; Bicarbonate ion; Bicarbonate ion, standard deviation; Biomass/Abundance/Elemental composition; Bise_seagrass; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbonate ion; Carbonate ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, standard deviation; Change in bacterial abundance; Change in bacterial abundance, standard deviation; Chlorophyll a, flux; Chlorophyll a, flux, standard deviation; Chlorophyll b, flux; Chlorophyll b, flux, standard deviation; Chlorophyll c2, flux; Chlorophyll c2, flux, standard deviation; Coast and continental shelf; Entire community; Event label; EXP; Experiment; Fucoxanthin, flux; Fucoxanthin, flux, standard deviation; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Gross primary production, standard deviation; Gross primary production of carbon; Habitat; Laboratory experiment; Light mode; Net primary production of carbon; Net primary production of carbon, standard deviation; Nitrite and nitrate, flux; Nitrite and nitrate, flux, standard deviation; North Pacific; OA-ICC; Ocean Acidification International Coordination Centre; Other metabolic rates; Oxygen, flux; Oxygen, flux, standard deviation; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, standard deviation; Phosphate, flux; Phosphate, flux, standard deviation; Potentiometric; Potentiometric titration; Primary production/Photosynthesis; Respiration; Respiration rate, carbon; Respiration rate, carbon dioxide, standard deviation; Salinity; Salinity, standard deviation; Sesoko_reef; Silicate, flux; Silicate, flux, standard deviation; Soft-bottom community; Temperate; Temperature; Temperature, water; Temperature, water, standard deviation; Treatment; Type; Yagachi_Island; Zeaxanthin, flux; Zeaxanthin, flux, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 3156 data points
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  • 2
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    Unknown
    PANGAEA
    In:  EPIC3WOCE., Bremerhaven, PANGAEA
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
    Format: application/pdf
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 57 (1985), S. 1840-1846 
    ISSN: 1520-6882
    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 Chemical Society
    The @journal of organic chemistry 54 (1989), S. 4732-4734 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1520-4804
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 88 (1988), S. 4739-4747 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The vibrational and rotational state distribution was measured for NO produced from the reaction O(1D)+N2O→2NO via a reactant pair O(1D)⋅N2O, which, in turn, formed by the 193 nm photolysis of the N2O dimer. The dimer was generated by the supersonic expansion through a pulsed nozzle. The distribution was determined by using the laser-induced fluorescence of NO on its A–X transition. The rotational distribution was of the Boltzmann type characterized by a low temperature, 60–100 K, at each vibrational level measured. The vibrational distribution was found to be composed of the two components, one very cold and the other relatively hot. The experiment using an isotopically labeled N2O revealed that the vibrational energy was not equally distributed over two kinds of NO; the NO originally present in N2O was vibrationally cool while that formed from O(1D) and the terminal nitrogen of N2O was vibrationally hot. These results indicate that the reaction occurring is the abstraction of the terminal nitrogen by O(1D). The low rotational temperature, which sharply contrasts with the extremely high rotational excitation observed for the ordinary bimolecular reaction, can be rationalized by considering the geometrical difference in the encounter between the O(1D) atom and N2O. This fact, in turn, indicates that the product energy distribution is significantly affected by the orientation in the reactive encounter.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 5960-5973 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The resonance secondary emission (RSE) in femtosecond laser excitation is discussed in reference to the motion of the created wave packet moving on the excited state potential surface. The density matrix of emitted light for the multi-intermediate-level system is outlined, from which the emission correlation function is derived. The correlation function is put into the theoretical expression of the time-dependent "physical spectrum'' for the Fabry–Perot interferometer (which is used in order to consider temporal and energetic resolution inherent in detection). The compact and practical expressions obtained connect the time- and frequency-resolved spectrum with the time evolution of the wave packet. Numerical results for a displaced harmonic oscillator model indicate that the time- and frequency-resolved spectrum can reveal how the wave packet created by a fs laser pulse travels on the excited potential surface if the response time 1/Γd of the photodetector satisfies the relation that Ω〈Γd 〈∼ the Stokes shift (where Ω is the vibrational frequency). It is shown that the excited state wave function can be split into two terms, the one that adiabatically follows the temporal change in incident light (the adiabatic term) and the one that represents the effect of spectral broadening of light (the Fourier broadening term). It is only the Fourier broadening term that survives after the termination of incident light and reflects the motion of the created wave packet on the excited potential surface. In off-resonance excitation, the adiabatic term produces Raman-like emission and the Fourier broadening one produces fluorescence-like emission. In resonance excitation, these two terms are indistinguishable from each other with respect to emission frequency: for the duration of incident light, the adiabatic term offsets the Fourier broadening one, leading to a slow buildup of intensity in the time- and frequency-resolved spectrum (which is slower than the initial rise of the incident pulse profile).
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 34-41 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Effects of the coherence transfer induced by the molecule–heat bath interactions on the ultrashort time-resolved coherent anti-Stokes Raman scattering (CARS) from molecules in liquids are theoretically studied. Based on the perturbative density matrix formalism an expression for the CARS intensity is derived taking into account the coherence transfer between the Raman active vibrational transitions of two molecules in liquids. The coherence transfer constants and dephasing constants are properly incorporated with the aid of Liouville space Feynman diagrams. The structure of the coherence transfer matrix element which expresses the time evolution of the coherence between the relevant transitions is clarified by solving the Master equation with the coherence transfer and dephasing constants in the Markoff approximation. Frequency shifts of the quantum beats appear in the time-resolved CARS as a result of the coherence transfer. A multispherical layer model is adopted in evaluating the coherence transfer effects in liquids in femtosecond time domains. Model calculations of time-resolved CARS spectra have been carried out to demonstrate the coherence transfer effects in both short and long range coherence transfer cases. It is predicted that the quantum beats are amplified in the time-resolved CARS spectra of molecules in liquids in a long range coherence transfer case when there exist differences in the coherence transfer constants between each spherical layer.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 3903-3915 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Effects of vibronic coherence transfer induced by the heat bath on ultrafast time-resolved resonant light scattering (RLS) spectra are theoretically investigated within the master equation approach. The vibronic coherence initially created by a coherent optical excitation transfers to other vibronic coherent states due to inelastic interactions between the vibronic system concerned (the relevant system) and the heat bath. The vibronic coherence transfer results in the quantum beats in the time-resolved RLS spectra. The bath-induced vibronic transition operator is derived in the double space representation of the density matrix theory. Model calculations of the femtosecond (fs) time-resolved RLS spectra are performed to demonstrate the effects of the bath-induced vibronic coherence transfer.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 85 (1999), S. 4076-4082 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Interfacial oxide structures were studied by Infrared reflection absorption spectroscopic analysis. The longitudinal optical mode of the interfacial oxide films arose with lower frequencies and wider widths. We assumed and later verified that these changes resulted from the contribution of interfacial roughness. We therefore examined the contribution of interfacial roughness to the infrared spectra using the effective medium approximation model and via infrared spectra simulation. The experimental results explained by a model of that interface had an atomically roughness of within 1 nm and chemical structure changes effectively little fluctuation. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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