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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 88 (2000), S. 2515-2518 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The 1.48-μm emission properties and electron population densities of the excited levels were investigated for Ge–As–Ga–S glasses doped with Tm3+ or Tm3+/Tb3+. Electron population inversion between the 3H4 and 3F4 levels in Tm3+ cannot be achieved without Tb3+ addition due to the strong cross-relaxation in Tm3+. Co-doping of Tb3+ resulted in the large decrease in the population density of the Tm3+:3F4 level via the energy transfer of Tm3+:3F4→Tb3+:7F0,1,2. Calculated population densities of the two levels in Tm3+ using the rate equations showed that the population inversion became possible through the addition of Tb3+. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Publication Date: 2024-01-06
    Description: This contribution to the RECCAP2 (REgional Carbon Cycle Assessment and Processes) assessment analyzes the processes that determine the global ocean carbon sink, and its trends and variability over the period 1985–2018, using a combination of models and observation-based products. The mean sea-air CO2 flux from 1985 to 2018 is −1.6 ± 0.2 PgC yr−1 based on an ensemble of reconstructions of the history of sea surface pCO2 (pCO2 products). Models indicate that the dominant component of this flux is the net oceanic uptake of anthropogenic CO2, which is estimated at −2.1 ± 0.3 PgC yr−1 by an ensemble of ocean biogeochemical models, and −2.4 ± 0.1 PgC yr−1 by two ocean circulation inverse models. The ocean also degasses about 0.65 ± 0.3 PgC yr−1 of terrestrially derived CO2, but this process is not fully resolved by any of the models used here. From 2001 to 2018, the pCO2 products reconstruct a trend in the ocean carbon sink of −0.61 ± 0.12 PgC yr−1 decade−1, while biogeochemical models and inverse models diagnose an anthropogenic CO2-driven trend of −0.34 ± 0.06 and −0.41 ± 0.03 PgC yr−1 decade−1, respectively. This implies a climate-forced acceleration of the ocean carbon sink in recent decades, but there are still large uncertainties on the magnitude and cause of this trend. The interannual to decadal variability of the global carbon sink is mainly driven by climate variability, with the climate-driven variability exceeding the CO2-forced variability by 2–3 times. These results suggest that anthropogenic CO2 dominates the ocean CO2 sink, while climate-driven variability is potentially large but highly uncertain and not consistently captured across different methods.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Format: application/pdf
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  • 3
    Publication Date: 2022-12-06
    Description: Author Posting. © American Geophysical Union, 2022. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 49(11), (2022): e2021GL097618, https://doi.org/10.1029/2021GL097618.
    Description: Krypton-81 dating provides new insights into the timing, mechanisms, and extent of meteoric flushing versus retention of saline fluids in the subsurface in response to changes in geologic and/or climatic forcings over 50 ka to 1.2 Ma year timescales. Remnant Paleozoic seawater-derived brines associated with evaporites in the Paradox Basin, Colorado Plateau, are beyond the 81Kr dating range (〉1.2 Ma) and have likely been preserved due to negative fluid buoyancy and low permeability. 81Kr dating of formation waters above the evaporites indicates topographically-driven meteoric recharge and salt dissolution since the Late Pleistocene (0.03–0.8 Ma). Formation waters below the evaporites (up to 3 km depth), in basal aquifers, contain relatively young meteoric water components (0.4–1.1 Ma based on 81Kr) that partially flushed remnant brines and dissolved evaporites. We demonstrate that recent, rapid denudation of the Colorado Plateau (〈4–10 Ma) activated deep, basinal-scale flow systems as recorded in 81Kr groundwater age distributions.
    Description: Funding for this research was provided by the W.M. Keck Foundation, CIFAR Earth 4D Subsurface Science and Exploration program, NSF EAR (#2120733), National Key Research and Development Program of China (Grant No. 2016YFA0302200), and National Natural Science Foundation of China (Grants No. 41727901). McIntosh and Ballentine are fellows of the CIFAR Earth4D Subsurface Science and Exploration program.
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 4
    Publication Date: 2022-10-26
    Description: © The Author(s), 2022. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Tyne, R., Barry, P., Cheng, A., Hillegonds, D., Kim, J.-H., McIntosh, J., & Ballentine, C. Basin architecture controls on the chemical evolution and 4He distribution of groundwater in the Paradox Basin. Earth and Planetary Science Letters, 589, (2022):117580, https://doi.org/10.1016/j.epsl.2022.117580.
    Description: Fluids such as 4He, H2, CO2 and hydrocarbons accumulate within Earth's crust. Crustal reservoirs also have potential to store anthropogenic waste (e.g., CO2, spent nuclear fuel). Understanding fluid migration and how this is impacted by basin stratigraphy and evolution is key to exploiting fluid accumulations and identifying viable storage sites. Noble gases are powerful tracers of fluid migration and chemical evolution, as they are inert and only fractionate by physical processes. The distribution of 4He, in particular, is an important tool for understanding diffusion within basins and for groundwater dating. Here, we report noble gas isotope and abundance data from 36 wells across the Paradox Basin, Colorado Plateau, USA, which has abundant hydrocarbon, 4He and CO2 accumulations. Both groundwater and hydrocarbon samples were collected from 7 stratigraphic units, including within, above and below the Paradox Formation (P.Fm) evaporites. Air-corrected helium isotope ratios (0.0046 - 0.127 RA) are consistent with radiogenic overprinting of predominantly groundwater-derived noble gases. The highest radiogenic noble gas concentrations are found in formations below the P.Fm. Atmosphere-derived noble gas signatures are consistent with meteoric recharge and multi-phase interactions both above and below the P.Fm, with greater groundwater-gas interactions in the shallower formations. Vertical diffusion models, used to reconstruct observed groundwater helium concentrations, show the P.Fm evaporite layer to be effectively impermeable to helium diffusion and a regional barrier for mobile elements but, similar to other basins, a basement 4He flux is required to accumulate the 4He concentrations observed beneath the P.Fm. The verification that evaporites are regionally impermeable to diffusion, of even the most diffusive elements, is important for sub-salt helium and hydrogen exploration and storage, and a critical parameter in determining 4He-derived mean groundwater ages. This is critical to understanding the role of basin stratigraphy and deformation on fluid flow and gas accumulation.
    Description: This work was supported by a Natural Environment Research Council studentship to R.L. Tyne (Grant ref. NE/L002612/1). We gratefully acknowledge the William F. Keck Foundation for support of this research, and the National Science Foundation (NSF EAR #2120733). J.C. McIntosh and C.J. Ballentine are fellows of the CIFAR Earth4D Subsurface Science and Exploration Program. The authors would like to acknowledge the U.S. Bureau of Reclamation, Paradox Resources, Navajo Petroleum, US Oil and Gas INC, Anson Resources, Lantz Indergard (Lisbon Valley Mining Co.), Ambria Dell'Oro and Mohammad Marza for help with sampling.
    Keywords: Noble gases ; Helium ; Paradox Basin ; Crustal fluid dating ; Groundwater migration
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 5
    Publication Date: 2013-11-26
    Description: We report pronounced enhancement of photoelectrochemical hydrogen generation of a quantum dot-sensitized hybrid-TiO2 (QD/H-TiO2) electrode that is composed of a mesoporous TiO2 layer sandwiched by a double sided energy harvesting layer consisting of a surface-textured TiO2 inverse opals layer on the bottom and a patterned mesoporous TiO2 layer on the top. CdSe/H-TiO2 exhibits a maximum photocurrent density of ~16.2 mA/cm2, which is 35% higher than that of the optimized control sample (CdSe/P25), achieved by matching of the bandgap of quantum dot-sensitization with the wavelength where light harvesting of H-TiO2 is observed. Furthermore, CdSe/H-TiO2 under filtered exposure conditions recorded current density of ~14.2 mA/cm2, the greatest value in the visible range. The excellent performance of the quantum dot-sensitized H-TiO2 suggests that alteration of the photoelectrodes to suitable nanostructures with excellent light absorption may offer optimal strategies for attaining maximum efficiency in a variety of photoconversion systems. Scientific Reports 3 doi: 10.1038/srep03330
    Electronic ISSN: 2045-2322
    Topics: Natural Sciences in General
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  • 6
    Publication Date: 2024-02-07
    Description: This contribution to the RECCAP2 (REgional Carbon Cycle Assessment and Processes) assessment analyzes the processes that determine the global ocean carbon sink, and its trends and variability over the period 1985-2018, using a combination of models and observation-based products. The mean sea-air CO2 flux from 1985 to 2018 is -1.6 +/- 0.2 PgC yr(-1) based on an ensemble of reconstructions of the history of sea surface pCO(2) (pCO(2) products). Models indicate that the dominant component of this flux is the net oceanic uptake of anthropogenic CO2, which is estimated at -2.1 +/- 0.3 PgC yr(-1) by an ensemble of ocean biogeochemical models, and -2.4 +/- 0.1 PgC yr(-1) by two ocean circulation inverse models. The ocean also degasses about 0.65 +/- 0.3 PgC yr(-1) of terrestrially derived CO2, but this process is not fully resolved by any of the models used here. From 2001 to 2018, the pCO2 products reconstruct a trend in the ocean carbon sink of -0.61 +/- 0.12 PgC yr(-1) decade(-1), while biogeochemical models and inverse models diagnose an anthropogenic CO2-driven trend of -0.34 +/- 0.06 and -0.41 +/- 0.03 PgC yr(-1) decade(-1), respectively. This implies a climate-forced acceleration of the ocean carbon sink in recent decades, but there are still large uncertainties on the magnitude and cause of this trend. The interannual to decadal variability of the global carbon sink is mainly driven by climate variability, with the climate-driven variability exceeding the CO2-forced variability by 2-3 times. These results suggest that anthropogenic CO2 dominates the ocean CO2 sink, while climate-driven variability is potentially large but highly uncertain and not consistently captured across different methods.
    Type: Article , PeerReviewed
    Format: text
    Format: text
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  • 7
    Publication Date: 2016-03-05
    Description: Erratum: How Do the Size, Charge and Shape of Nanoparticles Affect Amyloid β Aggregation on Brain Lipid Bilayer? Scientific Reports, Published online: 4 March 2016; doi:10.1038/srep22173
    Electronic ISSN: 2045-2322
    Topics: Natural Sciences in General
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  • 8
    Publication Date: 2016-07-01
    Description: Intrinsic FGF2 and FGF5 promotes angiogenesis of human aortic endothelial cells in 3D microfluidic angiogenesis system Scientific Reports, Published online: 30 June 2016; doi:10.1038/srep28832
    Electronic ISSN: 2045-2322
    Topics: Natural Sciences in General
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  • 9
    Publication Date: 2016-08-13
    Description: Organic Letters DOI: 10.1021/acs.orglett.6b02156
    Print ISSN: 1523-7060
    Electronic ISSN: 1523-7052
    Topics: Chemistry and Pharmacology
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  • 10
    Publication Date: 2016-06-15
    Description: The Journal of Physical Chemistry B DOI: 10.1021/acs.jpcb.6b02608
    Electronic ISSN: 1520-5207
    Topics: Chemistry and Pharmacology , Physics
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