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  • 1
    Publication Date: 2023-12-16
    Description: 〈title xmlns:mml="http://www.w3.org/1998/Math/MathML"〉Abstract〈/title〉〈p xmlns:mml="http://www.w3.org/1998/Math/MathML" xml:lang="en"〉Three volcanic arcs have been the source of New Zealand's volcanic activity since the Neogene: Northland arc, Coromandel Volcanic Zone (CVZ) and Taupō Volcanic Zone (TVZ). The eruption chronology for the Quaternary, sourced by the TVZ, is well studied and established, whereas the volcanic evolution of the precursor arc systems, like the CVZ (central activity c. 18 to 2 Ma), is poorly known due to limited accessibility to, or identification of, onshore volcanic deposits and their sources. Here, we investigate the marine tephra record of the Neogene, mostly sourced by the CVZ, of cores from IODP Exp. 375 (Sites U1520 and U1526), ODP Leg 181 (Sites 1123, 1124 and 1125), IODP Leg 329 (Site U1371) and DSDP Leg 90 (Site 594) offshore of New Zealand. In total, we identify 306 primary tephra layers in the marine sediments. Multi‐approach age models (e.g. biostratigraphy, zircon ages) are used in combination with geochemical fingerprinting (major and trace element compositions) and the stratigraphic context of each marine tephra layer to establish 168 tie‐lines between marine tephra layers from different holes and sites. Following this approach, we identify 208 explosive volcanic events in the Neogene between c. 17.5 and 2.6 Ma. This is the first comprehensive study of New Zealand's Neogene explosive volcanism established from tephrochronostratigraphic studies, which reveals continuous volcanic activity between c. 12 and 2.6 Ma with an abrupt compositional change at c. 4.5 Ma, potentially associated with the transition from CVZ to TVZ.〈/p〉
    Description: Plain Language Summary: Since 18 Ma, volcanic activity in New Zealand is dominantly sourced by the Coromandel Volcanic Zone (CVZ). Most caldera systems of the CVZ identified so far are located on Coromandel Peninsula in the NW of North Island, New Zealand, but studies of the CVZ are rare mainly due to the limited accessibility of its volcanic deposits, as well as missing stratigraphic continuity between different outcrops and the volcanic source. Here, our ocean drilling tephra record—mainly volcanic ash from explosive eruptions, distributed and falling out over the ocean—has a great potential to reveal the eruption history of the CVZ because it is preserved in marine sediments in a nearly undisturbed stratigraphic context. We analyzed ∼400 marine tephra layers from multiple ocean sediment cores off the coast of New Zealand for their geochemical glass compositions and identified 306 as largely undisturbed ash deposits. These primary ash deposits correspond to a total number of 208 Neogene volcanic events. Different dating methods result in a continuous marine tephra record for the last 12 Ma, equivalent to a unique and most complete eruptive history for the CVZ. This enables us to further unravel changes in the composition of the associated magmas with time.〈/p〉
    Description: Key Points: 〈list list-type="bullet"〉 〈list-item〉 〈p xml:lang="en"〉New Zealand's Neogene explosive volcanism based on the marine tephra record〈/p〉〈/list-item〉 〈list-item〉 〈p xml:lang="en"〉Geochemical fingerprinting of marine tephra layers across the study area to establish volcanic events〈/p〉〈/list-item〉 〈list-item〉 〈p xml:lang="en"〉Insights into geochemical variations with time, repose times and spatiotemporal distribution〈/p〉〈/list-item〉 〈/list〉 〈/p〉
    Description: DFG
    Description: Marsden project
    Description: https://doi.org/10.14379/iodp.proc.372B375.210.2023
    Keywords: ddc:551 ; marine tephrochronostratigraphy ; geochemical fingerprinting ; correlations of marine tephras between individual drill sites ; IODP ; ODP and DSDP drill sites ; neogene eruption record of New Zealand
    Language: English
    Type: doc-type:article
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  • 2
    Publication Date: 2021-07-21
    Description: The Tierra Blanca (TB) eruptive suite comprises the last four major eruptions of Ilopango caldera in El Salvador (≤45 ka), including the youngest Tierra Blanca Joven eruption (TBJ; ∼106 km3): the most voluminous event during the Holocene in Central America. Despite the protracted and productive history of explosive silicic eruptions at Ilopango caldera, many aspects regarding the longevity and the prevailing physicochemical conditions of the underlying magmatic system remain unknown. Zircon 238U‐230Th geochronology of the TB suite (TBJ, TB2, TB3, and TB4) reveals a continuous and overlapping crystallization history among individual eruptions, suggesting persistent melt presence in thermally and compositionally distinct magma reservoirs over the last ca. 80 kyr. The longevity of zircon is in contrast to previously determined crystallization timescales of 〈10 kyr for major mineral phases in TBJ. This dichotomy is explained by a process of rhyolitic melt segregation from a crystal‐rich refractory residue that incorporates zircon, whereas a new generation of major mineral phases crystallized shortly before eruption. Ti‐in‐zircon temperatures and amphibole geothermobarometry suggest that rhyolitic melt was extracted from different storage zones of the magma reservoir as indicated by distinct but synchronous thermochemical zircon histories among the TB suite eruptions. Zircon from TBJ and TB2 suggests magma differentiation within deeper and hotter parts of the reservoir, whereas zircon from TB3 and TB4 instead hints at crystallization in comparatively shallower and cooler domains. The assembly of the voluminous TBJ magma reservoir was also likely enhanced by cannibalization of hydrothermally altered components as suggested by low‐δ18O values in zircon (+4.5 ± 0.3‰).
    Description: Plain Language Summary: The collapse of a volcano edifice into its shallow magma chamber can produce one of the most dangerous single events in nature, known as a caldera‐forming eruption. The TBJ eruption in El Salvador is of this kind and occurred around 1,500 years ago, having a profound impact on Maya societies. Because of this, it is crucial to understand the inner workings of caldera‐forming eruptions to assess volcanic risks and their mitigation. Beneath Ilopango caldera, the micrometer‐sized radioisotopically datable mineral zircon grew within different storage levels of a silica‐rich magma reservoir suggesting continuous melt presence for up to ca. 80,000 years prior to eruption. The time information given by zircon contrasts with that extracted from other, more abundant minerals from the same rocks (〈10,000 years). We explain this time difference between coexisting minerals by the ability of melt to carry along small zircon crystals, whereas coeval, larger, and more abundant minerals are left behind in the partially solidified portion of the magma reservoir. Once the segregated melt coalesced in a shallower and dominantly liquid magma chamber, major minerals resumed crystallization shortly before eruption. In addition, this new magma incorporated parts of older magmatic rocks from preceding volcanic cycles, thus generating even larger magma volumes.
    Description: Key Points: U‐Th zircon ages for the last four explosive eruptions of Ilopango caldera reveal a long‐lived magma reservoir (〉80 kyr). Contrasting residence times for major minerals and zircon suggest extraction of zircon along with evolved melt from crystal residue. Melt extraction from vertically extensive, thermally zoned magma reservoir.
    Description: Deutsche Forschungsgemeinschaft (DFG) http://dx.doi.org/10.13039/501100001659
    Keywords: 549 ; 551.701 ; Central America ; Geochemistry ; Oxygen isotopes ; SIMS ; U‐series ; Zircon
    Type: article
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 34 (1962), S. 1587-1590 
    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
    Analytical chemistry 34 (1962), S. 164-166 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 113 (2000), S. 9622-9636 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The reaction between ground state carbon atoms, C(3Pj), and 1,3-butadiene, H2CCHCHCH2, was studied at three averaged collision energies between 19.3 and 38.8 kJmol−1 using the crossed molecular beam technique. Our experimental data combined with electronic structure calculations show that the carbon atom adds barrierlessly to the π-orbital of the butadiene molecule via a loose, reactantlike transition state located at the centrifugal barrier. This process forms vinylcyclopropylidene which rotates in a plane almost perpendicular to the total angular momentum vector J around its C-axis. The initial collision complex undergoes ring opening to a long-lived vinyl-substituted triplet allene molecule. This complex shows three reaction pathways. Two distinct H atom loss channels form 1- and 3-vinylpropargyl radicals, HCCCHC2H3(X2A″) and H2CCCC2H3(X2A″), through tight exit transition states located about 20 kJmol−1 above the products; the branching ratio of 1- versus 3-vinylpropargyl radical is about 8:1. A minor channel of less than 10% is the formation of a vinyl, C2H3(X2A′), and propargyl radical C3H3(X2B2). The unambiguous identification of two C5H5 chain isomers under single collision has important implications to combustion processes and interstellar chemistry. Here, in denser media such as fuel flames and in circumstellar shells of carbon stars, the linear structures can undergo a collision-induced ring closure followed by a hydrogen migration to cyclic C5H5 isomers such as the cyclopentadienyl radical—a postulated intermediate in the formation of polycyclic aromatic hydrocarbons (PAHs). © 2000 American Institute of Physics.
    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 113 (2000), S. 9637-9648 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The reaction of ground state carbon atoms, C(3Pj), with dimethylacetylene, H3CCCCH3, was studied at three collision energies between 21.2 and 36.9 kJmol−1 employing the crossed molecular beam approach. Our experiments were combined with ab initio and RRKM calculations. It is found that the reaction is barrierless via a loose, early transition state located at the centrifugal barrier following indirect scattering dynamics through a complex. C(3Pj) attacks the π system of the dimethylacetylene molecule to form a dimethylcyclopropenylidene intermediate either in one step via an addition to C1 and C2 of the acetylenic bond or through an addition to only one carbon atom to give a short-lived cis/trans dimethylpropenediylidene intermediates followed by ring closure. The cyclic intermediate ring opens to a linear dimethylpropargylene radical which rotates almost parallel to the total angular momentum vector J. This complex fragments to atomic hydrogen and a linear 1-methylbutatrienyl radical, H2CCCCCH3(X2A″), via a tight exit transition state located about 18 kJmol−1 above the separated products. The experimentally determined exothermicity of 190±25 kJmol−1 is in strong agreement with our calculated data of 180±10 kJmol−1. The explicit verification of the carbon versus hydrogen exchange pathway together with the first identification of the H2CCCCCH3 radical represents a third pathway to form chain C5H5 radicals in the reactions of C(3Pj) with C4H6 isomers under single collision conditions. Previous experiments of atomic carbon with the 1,3-butadiene isomer verified the formation of 1- and 3-vinylpropargyl radicals, HCCCHC2H3(X2A″), and H2CCCC2H3(X2A″), respectively. In high-density environments such as combustion flames and circumstellar envelopes of carbon stars, these linear isomers can undergo collision-induced ring closure(s) and/or H atom migration(s) which can lead to the cyclopentadienyl radical. The latter is thought to be a crucial reactive intermediate in soot formation and possibly in the production of polycyclic aromatic hydrocarbon molecules in outflow of carbon stars. Likewise, a H atom catalyzed isomerization can interconvert the 3-vinylpropargyl and the 1-methylbutatrienyl radical. © 2000 American Institute of Physics.
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  • 7
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Crossed molecular beam experiments were conducted to investigate the reaction of ground state carbon atoms, C(3Pj), with 1,2-butadiene, H2CCCH(CH3) (X 1A′), at three collision energies of 20.4 kJ mol−1, 37.9 kJ mol−1, and 48.6 kJ mol−1. Ab initio calculations together with our experimental data reveal that the reaction is initiated by a barrier-less addition of the carbon atom to the π system of the 1,2-butadiene molecule. Dominated by large impact parameters, C(3Pj) attacks preferentially the C2–C3 double bond to form i1 (mechanism 1); to a minor extent, small impact parameters lead to an addition of atomic carbon to the C1–C2 bond yielding i2 (mechanism 2). Both cyclic intermediates i1 and i2 ring open to triplet methylbutatriene complexes i3′ (H2CC*CCH(CH3)) and i3″, (H2CCC*CH(CH3)); C* denotes the attacked carbon atom. i3′ is suggested to decay nonstatistically prior to a complete energy randomization via atomic hydrogen loss forming 1- and 4-methylbutatrienyl CH3CCCCH2 (X 2A″) and HCCCCH(CH3) (X 2A″), respectively. The energy randomization in i3″ is likely to be complete. This isomer decomposes via H atom loss to 3-vinylpropargyl, H2CCCC2H3(X 2A″), as well as 1- and 4-methylbutatrienyl radicals. In high-density environments such as the inner regions of circumstellar envelopes of carbon stars and combustion flames, these linear C5H5 isomers might undergo collision induced isomerization to cyclic structures like the cyclopentadienyl radical. This isomer is strongly believed to be a key intermediate involved in the production of polycyclic aromatic hydrocarbon molecules and soot formation. These characteristics make the reactions of atomic carbon with C4H6 isomers compelling candidates to form C5H5 isomers in the outflow of AGB stars and oxygen-deficient hydrocarbon flames. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of food science 63 (1998), S. 0 
    ISSN: 1750-3841
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Phase transfer experiments were performed, involving contact between an aqueous 1:1 solution of α-lactalbumin and β-lactoglobulin and an AOT-in-isooctane reversed micellar phase. The resulting extraction and separation of the two proteins were analyzed as functions of pH, ionic strength and total protein concentration using SDS-PAGE, and compared with extractions from pure solutions. At low protein concentrations, the extent of reversed micellar solubilization of the two pure proteins predicted well the extraction from mixtures. However, at higher protein concentrations β-lactoglobulin appeared to be excluded from the micellar droplets. Because of the significantly different partitioning behavior of the two proteins, reversed micellar extraction from an initially equal weight mixture led to an effective separation of the proteins.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 65 (1989), S. 3928-3932 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Defect levels in n-type Si Schottky barrier diodes made by resistive evaporation have been investigated by deep level transient spectroscopy. Three defect levels are observed at 0.16, 0.14, and 0.12 eV below the conduction band. The concentrations of the defect levels exponentially decrease into the substrate. The defects are introduced during etching process rather than evaporation process. The concentration of the defects increase with the thickness of the layer removed by etching before Schottky metal deposition, and decrease with the etching rate. This suggests that the defect levels are produced near the surface and are driven into the substrate during etching processes.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 55 (1989), S. 2322-2324 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Lattice-matched InGaP/GaAs superlattices have been grown by gas-source molecular beam epitaxy. High-resolution images obtained with transmission electron microscopy reveal the superlattices to be free of dislocations and to exhibit smooth interfaces of only 1–2 monolayers in width. Double crystal x-ray diffraction studies indicate that the narrow interfacial regions are locally strained as a result of the growth sequence during gas-source molecular beam epitaxy.
    Type of Medium: Electronic Resource
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