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  • Springer Nature  (258)
  • Geological Society of London  (71)
  • American Institute of Physics (AIP)  (64)
  • Geological Society of America (GSA)
  • Amsterdam : Elsevier
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  • 1
    Monograph available for loan
    Monograph available for loan
    EUROPROBE GeoRift, volume 2 : intraplate tectonics and basin dynamics of the eastern european craton and its margins (1999)
    Amsterdam : Elsevier
    Associated volumes
    Details Availability
    Call number: ILP/M 06.0347
    In: Publication of the International Lithosphere Programme
    In: Tectonophysics
    Type of Medium: Monograph available for loan
    Pages: ix, 241 S. : Ill., graph. Darst.
    Series Statement: [Publication of the International Lithosphere Programme] 313,1-2 : special issue
    Language: English
    Location: Reading room
    Branch Library: GFZ Library
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  • 2
    Monograph available for loan
    Monograph available for loan
    EUROPROBE, GeoRift 3 : intraplate tectonics and basin dynamics ; the lithosphere of the southern eastern european craton and its margin (2004)
    Amsterdam : Elsevier
    Associated volumes
    Details Availability
    Call number: ILP/M 06.0353
    In: Publication of the International Lithosphere Programme
    In: Tectonophysics
    Type of Medium: Monograph available for loan
    Pages: vi, 271 S. : Ill., graph. Darst.
    Series Statement: [Publication of the International Lithosphere Programme] 381,1-4 : special issue
    Language: English
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  • 3
    Monograph available for loan
    Monograph available for loan
    EUROPROBE: intraplate tectonics and basin dynamics of the eastern european platform : selected papers presented at the EUROPROBE ITBD workshop held in Vorzel (near Kiev), Ukraine, Oct. 1994 (1996)
    Amsterdam : Elsevier
    Associated volumes
    Details Availability
    Call number: ILP/M 06.0340
    In: Publication of the International Lithosphere Programme
    In: Tectonophysics
    Type of Medium: Monograph available for loan
    Pages: x, 309 S. : graph. Darst.
    Series Statement: [Publication of the International Lithosphere Programme] 268,1-4 : special issue
    Language: English
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  • 4
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    Culture and Sustainability (2023)
    Springer Nature | Palgrave Macmillan
    Details
    Publication Date: 2024-03-29
    Description: This Open access book brings a cultural lens, and a distinctive analytical framework, to the problem of transitioning to a sustainable, low-carbon future. The world faces a seemingly impossible hurdle – to radically alter long-established social, economic and technological systems in order to live within the biophysical limits of the globe, while ensuring a just and enduring transition. The overarching premise of this book is that this cannot be achieved without widespread cultural change. ‘We need a change in culture’ is often used rhetorically, but what does this really mean? Stephenson starts by exploring culture’s elusiveness, describing its divergent interpretations before identifying core features of culture that are common across most definitions. These characteristics form the core of the cultures framework, an extensively tested approach to studying the links between culture and sustainability outcomes. The framework makes culture an accessible concept which can be analytically applied to almost any sustainability problem. Using many examples from around the world, Stephenson illustrates how cultural stability, cultural flexibility and cultural transformation all have a part to play in the sustainability transition. She guides the reader in the use of the cultures framework for policy development and to underpin research undertaken by individuals or by multi-disciplinary teams. Clearly and engagingly written, Culture and Sustainability is essential reading for academics, students, policy makers and indeed anyone interested in a sustainable future.
    Keywords: sustainable transitions ; low carbon transition ; energy transition ; sustainability ; sustainable development goals ; culture and sustainability ; energy cultures ; culture framework ; socio-technical transitions ; thema EDItEUR::J Society and Social Sciences::JP Politics and government::JPQ Central / national / federal government::JPQB Central / national / federal government policies ; thema EDItEUR::J Society and Social Sciences::JH Sociology and anthropology::JHB Sociology ; thema EDItEUR::R Earth Sciences, Geography, Environment, Planning::RG Geography ; thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GT Interdisciplinary studies::GTP Development studies ; thema EDItEUR::R Earth Sciences, Geography, Environment, Planning::RN The environment::RNU Sustainability ; thema EDItEUR::J Society and Social Sciences::JB Society and culture: general::JBS Social groups, communities and identities::JBSR Social groups: religious groups and communities
    Language: English
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  • 5
    Electronic Resource
    Electronic Resource
    CO(v=1) population lifetimes of metal–carbonyl cluster compounds in dilute CHCl3 solution (1988)
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 230-239 
    Details
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Tunable infrared picosecond pulses in the 5 μ region have been used for time-resolved pump–probe measurements of the population relaxation lifetime (T1) of CO(v=1) stretching vibrations in a series of metal–carbonyl cluster compounds in room temperature chloroform solution. T1 was the same for symmetric (ν=2084 cm−1, 90±10 ps) and antisymmetric (2014 cm−1, 87±10 ps) modes of the dicarbonyl Rh(CO)2(C5H7O2); T1 was the same for the B1 (2092 cm−1 , 710±130 ps) and B2 (2036 cm−1, 750±90 ps) modes of Rh2(CO)4Cl2. Similarly long T1 times were found for Rh4(CO)12 (2075 cm−1, 610±65 ps) and Rh6(CO)16 (2077 cm−1, 700±100 ps). The molecule Co4(CO)12 has also been compared to the corresponding rhodium analog and it exhibits an initially fast relaxation of 47±5 ps followed by a slower 396±70 ps decay. The transient response of the more complex systems to the single frequency experiment is found to be sensitive to frequency and can exhibit bleaching, absorption, and a combination of these effects. Such behavior is attributed to overlap of the IR pulse with v=1 to v=2 and higher transitions in the M4(CO)12 (M=Rh or Co) and Rh6(CO)16 molecules. The long CO(v=1) T1 values for the metal cluster molecules suggest relaxation via multiquantum transfer of vibrational energy to adjacent M–C stretch and M–C–O bend vibrations; energy transfer to vibrational or electronic states of the central metal core seems unimportant in determining T1 for these systems.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.455510
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  • 6
    Electronic Resource
    Electronic Resource
    Unimolecular dynamics following vibrational overtone excitation of HN3 v1=5 and v1=6: HN3(X˜;v,J,K)→HN(X 3Σ−;v,J,Ω)+N2 (X 1Σ+g) (1988)
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 608-609 
    Details
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Excitation of the NH-stretch overtone transitions of HN3 to v1=5 and 6 resulted in predissociation to HN(X) and N2(X) with lifetimes of 80+60−30 and ≤3 ns, respectively. Following excitation of either overtone, the HN fragments were formed predominantly in the symmetric F1, F3 spin–rotation states, with less than 4% population in the antisymmetric F2 levels. Fragment Doppler profiles confirmed that most of the available energy (〉96%) went into translational motion.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.455454
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  • 7
    Electronic Resource
    Electronic Resource
    Nonadiabatic electronic interactions in the ion-pair states of NeICl (1991)
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 4171-4181 
    Details
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Nonadiabatic interactions in the NeICl van der Waals complex have been explored in the lowest energy triad of ICl ion-pair states (∼39 000 cm−1). Dispersed fluorescence measurements reveal emission characteristic of multiple ion-pair electronic states, with the relative contributions from the E(0+), β(1), and D'(2) states changing with the initial ICl vibrational excitation (vICl). Emission directly from NeICl (vICl=0) complexes indicates that the initially prepared NeICl levels have mixed electronic character and that the ICl electronic parentage changes with the initial van der Waals vibrational level selected. NeICl complexes prepared with 1–4 quanta of ICl stretch undergo rapid vibrational predissociation with a strong propensity for ΔvICl=−1 relaxation. The electronic state(s) populated in the ICl fragments differ from the mixed electronic character of the initially prepared level, demonstrating that vibrational predissociation is accompanied by nonadiabatic electronic state changing processes. The observed final state selectivity may be attributed to the relative strength of the nonadiabatic couplings between the initial NeICl bound state and the final ICl states or a momentum gap rationale based on the overlap between the NeICl bound state wave function and the highly oscillatory continuum wave function of the separating fragments.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.460650
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  • 8
    Electronic Resource
    Electronic Resource
    Fragment energy and vector correlations in the overtone-pumped dissociation of HN3 X˜ 1A' (1991)
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 250-261 
    Details
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: NH stretching overtone and combination states in HN3 X˜ 1A' were excited by IR–visible double resonance pumping and by direct overtone pumping in the range 6ν1 (17 670 cm−1) to 7ν1 (20 070 cm−1). NH fragments in the a 1Δ and X 3Σ− states were detected by laser induced fluorescence with sub-Doppler resolution to determine branching ratios, correlated fragment rotational state and kinetic energy distributions, and fragment vector correlations. The spin-forbidden triplet channel was accessible to all states excited, while the threshold for the singlet channel was determined to lie in the range 18 190 to 18 755 cm−1. The measured energy release places limits on the HN–NN bond energy, and the heights of barriers to reaction. The barrier in the singlet exit channel is at least 540 cm−1. The singlet channel accessed by 7ν1 dissociation is characterized by a Boltzmann-like NH rotational distribution (〈J NH〉≈3.5), highly excited N2 rotations (〈JN2〉 ≥ 20), and total translational energy release peaked away from zero (〈ET〉≈1350 cm−1). Vector correlations and Λ-doublet propensities indicate that nonplanar dissociation processes influence the NH rotations, but become less important for higher NH rotational states. The principal correlations are a strong positive recoil anisotropy (β≈0.6), a weak positive v–J correlation (βvJ≈0.17), and a JNH-dependent Λ-doublet propensity. A model using parent vibrational motion projected onto fragment rotation is suggested to explain these observations. The triplet channel exhibits similar NH and N2 rotational state distributions, with most of the available energy (substantially greater than in the singlet channel) appearing as fragment kinetic energy.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.460392
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  • 9
    Electronic Resource
    Electronic Resource
    Energetics and spin- and Λ-doublet selectivity in the infrared multiphoton dissociation DN3→DN(X 3Σ−, a 1Δ)+N2(X 1Σ+g): Experiment (1988)
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 1378-1387 
    Details
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Multiphoton vibrational excitation of deuterated hydrazoic acid, DN3, by a CO2 laser (I=10 GW/cm2) leads to dissociation forming DN in both X 3Σ− (spin forbidden) and a 1Δ (spin allowed) electronic states. Under collisionless conditions, the nascent DN fragments were probed via laser induced fluorescence, to determine initial product state distributions. The DN(X 3Σ−) molecules are formed predominantly in the symmetric F1 and F3 spin–rotation states with little population (≤6%) in the antisymmetric F2 levels. There is no significant population (〈3%) in excited DN(3Σ−) vibrational levels. The distribution of rotational states is Boltzmann-like, characterized by a rotational "temperature'' of about 920 K for the F1, F3 states and 500 K for F2 levels. Doppler profiles showed a large kinetic energy release of about 10 100 cm−1 total in the triplet channel. The DN(1Δ) products are formed preferentially in the symmetric Δ(A'), e-labeled lambda doublet levels: Δ(A')/Δ(A‘)=1.44. The DN(1Δ) is formed with no vibrational excitation (〈2%); the rotational states are populated Boltzmann-like with a rotational "temperature'' of 425 K. Doppler profiles give a total kinetic energy of about 1500 cm−1 in this channel. These observations give information about the distribution of energy in the reactant, the location of the barriers to dissociation, and the geometry of the transition states. Alexander, Werner, and Dagdigian (accompanying article) show that the observed DN(3Σ−) spin- and DN(1Δ) Λ-doublet selectivities reflect the symmetry properties of a planar transition state and that the low degree of DN(3Σ−) rotational and vibrational excitation is also expected from the transition state geometry.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.455137
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  • 10
    Electronic Resource
    Electronic Resource
    Population lifetimes of OH(v=1) and OD(v=1) stretching vibrations of alcohols and silanols in dilute solution (1986)
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 85 (1986), S. 5004-5018 
    Details
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Picosecond infrared pump–probe experiments determined the vibrational population lifetimes (T1) of the hydroxyl fundamental stretching mode OH(v=1) in 12 alcohols (R3COH) and 8 silanols (R3SiOH) in dilute room temperature CCl4 solutions. T1 for the silanols is in the range 185〈T1〈292 ps, while T1 for the alcohols is much less (T1〈80 ps). The deuterium-exchanged analogs (COD and SiOD) exhibit population relaxation times similar to protonated hydroxyls. An analysis of the vibrational energy levels corresponding to modes involving the four bonds nearest the hydroxyl groups of these molecules is used to qualitatively explain the trends of the observed T1 lifetimes for these systems. Solution T1 lifetimes are also compared to those previously measured for OH(v=1) on the surface of silica and in other condensed-phase, room temperature systems.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.451690
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