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Reconstructing Oligocene–Miocene paleoelevation contributes to our understanding of the evolutionary history of the European Alps and sheds light on geodynamic and Earth surface processes involved in the development of Alpine topography. Despite being one of the most intensively explored mountain ranges worldwide, constraints on the elevation history of the European Alps remain scarce. Here we present stable and clumped isotope measurements to provide a new paleoelevation estimate for the mid-Miocene (∼14.5 Ma) European Central Alps. We apply stable isotope δ–δ paleoaltimetry to near-sea-level pedogenic carbonate oxygen isotope (δ18O) records from the Northern Alpine Foreland Basin (Swiss Molasse Basin) and high-Alpine phyllosilicate hydrogen isotope (δD) records from the Simplon Fault Zone (Swiss Alps). We further explore Miocene paleoclimate and paleoenvironmental conditions in the Swiss Molasse Basin through carbonate stable (δ18O, δ13C) and clumped (Δ47) isotope data from three foreland basin sections in different alluvial megafan settings (proximal, mid-fan, and distal). Combined pedogenic carbonate δ18O values and Δ47 temperatures (30±5 ∘C) yield a near-sea-level precipitation δ18Ow value of ‰ and, in conjunction with the high-Alpine phyllosilicate δD value of ‰, suggest that the region surrounding the Simplon Fault Zone attained surface elevations of >4000 m no later than the mid-Miocene. Our near-sea-level δ18Ow estimate is supported by paleoclimate (iGCM ECHAM5-wiso) modeled δ18O values, which vary between −4.2 ‰ and −7.6 ‰ for the Northern Alpine Foreland Basin.
Stratospheric inorganic chlorine (Cly) is predominantly released from long-lived chlorinated source gases and, to a small extent, very short-lived chlorinated substances. Cly includes the reservoir species (HCl and ClONO2) and active chlorine species (i.e., ClOx). The active chlorine species drive catalytic cycles that deplete ozone in the polar winter stratosphere. This work presents calculations of inorganic chlorine (Cly) derived from chlorinated source gas measurements on board the High Altitude and Long Range Research Aircraft (HALO) during the Southern Hemisphere Transport, Dynamic and Chemistry (SouthTRAC) campaign in austral late winter and early spring 2019. Results are compared to Cly in the Northern Hemisphere derived from measurements of the POLSTRACC-GW-LCYCLE-SALSA (PGS) campaign in the Arctic winter of 2015/2016. A scaled correlation was used for PGS data, since not all source gases were measured. Using the SouthTRAC data, Cly from a scaled correlation was compared to directly determined Cly and agreed well. An air mass classification based on in situ N2O measurements allocates the measurements to the vortex, the vortex boundary region, and midlatitudes. Although the Antarctic vortex was weakened in 2019 compared to previous years, Cly reached 1687±19 ppt at 385 K; therefore, up to around 50 % of total chlorine was found in inorganic form inside the Antarctic vortex, whereas only 15 % of total chlorine was found in inorganic form in the southern midlatitudes. In contrast, only 40 % of total chlorine was found in inorganic form in the Arctic vortex during PGS, and roughly 20 % was found in inorganic form in the northern midlatitudes. Differences inside the two vortices reach as much as 540 ppt, with more Cly in the Antarctic vortex in 2019 than in the Arctic vortex in 2016 (at comparable distance to the local tropopause). To our knowledge, this is the first comparison of inorganic chlorine within the Antarctic and Arctic polar vortices. Based on the results of these two campaigns, the differences in Cly inside the two vortices are substantial and larger than the inter-annual variations previously reported for the Antarctic.
Biogenic organic precursors play an important role in atmospheric new particle formation (NPF). One of the major precursor species is α-pinene, which upon oxidation can form a suite of products covering a wide range of volatilities. Highly oxygenated organic molecules (HOMs) comprise a fraction of the oxidation products formed. While it is known that HOMs contribute to secondary organic aerosol (SOA) formation, including NPF, they have not been well studied in newly formed particles due to their very low mass concentrations. Here we present gas- and particle-phase chemical composition data from experimental studies of α-pinene oxidation, including in the presence of isoprene, at temperatures (−50 and −30 ∘C) and relative humidities (20 % and 60 %) relevant in the upper free troposphere. The measurements took place at the CERN Cosmics Leaving Outdoor Droplets (CLOUD) chamber. The particle chemical composition was analyzed by a thermal desorption differential mobility analyzer (TD-DMA) coupled to a nitrate chemical ionization–atmospheric pressure interface–time-of-flight (CI-APi-TOF) mass spectrometer. CI-APi-TOF was used for particle- and gas-phase measurements, applying the same ionization and detection scheme. Our measurements revealed the presence of C8−10 monomers and C18−20 dimers as the major compounds in the particles (diameter up to ∼ 100 nm). Particularly, for the system with isoprene added, C5 (C5H10O5−7) and C15 compounds (C15H24O5−10) were detected. This observation is consistent with the previously observed formation of such compounds in the gas phase. However, although the C5 and C15 compounds do not easily nucleate, our measurements indicate that they can still contribute to the particle growth at free tropospheric conditions. For the experiments reported here, most likely isoprene oxidation products enhance the growth of particles larger than 15 nm. Additionally, we report on the nucleation rates measured at 1.7 nm (J1.7 nm) and compared with previous studies, we found lower J1.7 nm values, very likely due to the higher α-pinene and ozone mixing ratios used in the present study.
Vor dem Hintergrund der zunehmenden Veränderung des städtischen Lebensumfeldes durch Gentrifizierung, investorenfreundliche Stadtpolitik, Privatisierung öffentlicher Räume, Einsparung öffentlicher Investitionen und den Abbau demokratischer Beteiligungsinstrumente haben wir uns gefragt: Wie könnte eine solidarische Stadt der Zukunft aussehen? Welche Gegenentwürfe zu aktuell herrschenden Paradigmen in der Stadtentwicklung zeigen uns Wege aus der Alternativlosigkeit hin zu einer solidarischen Praxis auf Quartiersebene? Im Rahmen einer angewandten kritischen Geografie möchten wir zeigen, dass es eine Vielzahl an Projekten und Initiativen gibt, die die Kreativlosigkeit, zu der uns der Neoliberalismus erzogen hat, durchbrechen und an konkreten Ideen und deren praktischer Umsetzung arbeiten. Als theoretische Annäherung dafür setzen wir uns mit Utopien und deren Potenzialen für eine politische Praxis auseinander. Da wir selbst im Kontext stadtpolitischer Gruppen engagiert sind, nutzen wir die aktivistische Stadtforschung als methodischen Rahmen unserer Forschung. Daraus entstanden ist ein Faltblatt, der „Kompass für ein solidarisches Quartier“, welcher als aktivistisches Werkzeug und Ideengeber für die konkrete Umsetzung transformativer Stadtpolitik dienen soll.
Lightning climate change projections show large uncertainties caused by limited empirical knowledge and strong assumptions inherent to coarse-grid climate modeling. This study addresses the latter issue by implementing and applying the lightning potential index parameterization (LPI) into a fine-grid convection-permitting regional climate model (CPM). This setup takes advantage of the explicit representation of deep convection in CPMs and allows for process-oriented LPI inputs such as vertical velocity within convective cells and coexistence of microphysical hydrometeor types, which are known to contribute to charge separation mechanisms. The LPI output is compared to output from a simpler flash rate parameterization, namely the CAPE × PREC parameterization, applied in a non-CPM on a coarser grid. The LPI’s implementation into the regional climate model COSMO-CLM successfully reproduces the observed lightning climatology, including its latitudinal gradient, its daily and hourly probability distributions, and its diurnal and annual cycles. Besides, the simulated temperature dependence of lightning reflects the observed dependency. The LPI outperforms the CAPE × PREC parameterization in all applied diagnostics. Based on this satisfactory evaluation, we used the LPI to a climate change projection under the RCP8.5 scenario. For the domain under investigation centered over Germany, the LPI projects a decrease of 4.8% in flash rate by the end of the century, in opposition to a projected increase of 17.4% as projected using the CAPE × PREC parameterization. The future decrease of LPI occurs mostly during the summer afternoons and is related to (i) a change in convection occurrence and (ii) changes in the microphysical mixing. The two parameterizations differ because of different convection occurrences in the CPM and non-CPM and because of changes in the microphysical mixing, which is only represented in the LPI lightning parameterization.
Global analysis of halogenated trace gases in the UTLS: from long-lived to short-lived substances
(2023)
In this dissertation, the distribution of chlorinated and brominated substances in the upper troposphere and lower stratosphere is investigated. These substances contribute significantly to the catalytic decomposition of ozone and are involved in the recurrent formation of the polar ozone hole in the Antarctic winter and spring. The Montreal Protocol, a multilateral environmental treaty to protect the ozone layer, has successfully reduced emissions of long-lived chlorine- and bromine-containing substances. Short-lived chlorinated and brominated substances, some of which are natural and anthropogenic in origin, are not regulated by the Montreal Protocol and it can be assumed that their relative contribution to the stratospheric halogen budget will increase, while the contribution of long-lived compounds will steadily decrease. The distribution of long- and short-lived halogenated substances are part of current research. For the upper troposphere and lower stratosphere, the very short-lived substances are particularly important. The lower stratosphere needs special investigation in this respect, since its composition is influenced by different transport processes. The influences on ozone trends in the lower stratosphere are subject to great uncertainties. Especially in the Southern Hemisphere, the number of observations is very limited.
In this work, the GhOST (Gas chromatograph for Observational Studies using Tracers) instrument was used during the SouthTRAC measurement campaign on the German HALO (High Altitude and LOng range) research aircraft, providing observations of halogenated hydrocarbons in Antarctic late winter to early spring 2019, a generally poorly sampled region. The polar vortex was, compared to previous years, significantly weaker and shifted towards the eastern South Pacific and South America. From the airborne measurements of chlorinated source gases, inorganic chlorine (the sum of active chlorine and reservoir gases; Cly) could be inferred with the result that Cly within the vortex increased up to 1687 ± 19 ppt at 385 K potential temperature, accounting for about 50 % of the total chlorine within the vortex and only 15 % of the total chlorine in the southern mid-latitudes. A comparison with the Northern Hemisphere could be made using the PGS measurement campaign in the Arctic winter 2015/2016. Under comparable conditions (season and distance from the tropopause), only 40 % of the total chlorine was in the inorganic form within the Arctic polar vortex and about 20 % was found in the mid-latitudes of the Northern Hemisphere. In addition, about 540 ppt more Cly was present in the Antarctic vortex than in the Arctic vortex, exceeding the annual variations previously reported for Antarctica.
The mean age of air plays an essential role in the derivation of Cly via the organic source gases, as was done in this work. A new method for determining the mean age of air from observational data has been introduced that accounts for extra-tropical input to the stratosphere in addition to tropical input. This new method was compared with the previously used method, which considered only the tropical input. The new method shows more realistic values especially near the tropopause. On average, the air of the lower stratosphere in the Northern Hemisphere was older than in the Southern Hemisphere by about 0.5 ± 0.3 years. About 65 K above the tropopause, the pattern changed with older air in the mid-latitudes of the Northern Hemisphere, but older air in high latitudes of the Southern Hemisphere, which implies differences in the strength and isolation of the respective polar vortex as well as the wave forcing in the shallow branch of the Brewer-Dobson circulation of the respective hemisphere. This is in good agreement with the distribution of Cly. The difference in the lower stratosphere was not clearly evident with the old method and it can be assumed that investigations of the differences in Cly of Northern and Southern Hemisphere will benefit from the new method.
Finally, the global and seasonal distribution of the two most important representatives of the short-lived brominated substances, CH2Br2 and CHBr3, was investigated. For this purpose, two additional HALO measurement campaigns have been used, the 2012 TACTS measurement campaign and the 2017 WISE measurement campaign, as well as the HIAPER Pole-to-Pole Observations (HIPPO) and Atmospheric Tomography (ATom) measurement campaigns. Observations of CH2Br2 show a pronounced seasonality in the free and upper troposphere of both hemispheres with slightly larger values in the Northern Hemisphere. CHBr3, on the other hand, shows a generally higher variability and lower seasonality with larger mixing ratios at mid and high latitudes in the northern hemispheric winter and autumn. A comparison of the lower stratosphere is limited to autumn and spring of both hemispheres due to the limited data basis of the observations. The distributions in each spring are similar (less than 0.1 ppt differences for e.g., CH2Br2). In hemispheric autumn, larger differences are evident with substantially smaller mixing ratios in the southern hemispheric lower stratosphere. This suggests that the transport processes of the two hemispheres may be different and implies that the input of tropospheric air (flushing) to the Northern Hemisphere lowest stratosphere is more efficient than in the Southern Hemisphere. Vertical profiles of CH2Br2 and CHBr3 in the mid-latitudes of both hemispheres and resulting vertical gradients support this conjecture. However, the Southern Hemisphere data set is insufficient to quantify this difference and further measurements are needed.
First-principles modeling techniques offer the ability to simulate a wide range of systems under different physical conditions, such as temperature, pressure, and composition, without relying on empirical knowledge. Density functional theory (DFT), a quantum mechanical method, has become an exceptionally successful framework for materials science modeling. Employing DFT makes it possible to gain valuable insights into the fundamental state of a system, enabling the reliable determination of equilibrium crystal structures. Over time, DFT has become an essential tool that can be incorporated into various schemes for predicting the properties of a material related to its structure, insulating/metallic behavior, magnetism, and optics. DFT is regularly applied in numerous fields, spanning from fundamental subjects in condensed matter physics to the study of large-scale phenomena in geosciences. In the latter, the effectiveness of DFT stems from its ability to simulate the properties found on the Earth, other planets, and meteorites, which may pose challenges for their direct study or laboratory investigation.
In this thesis, a comprehensive examination of a family of monosulfides and a perovskite heterostructure was conducted. These materials are relevant for their potential applications in technology, energy harvesting, and in the case of monosulfides, their speculated abundance on the planet Mercury.
Firstly, a DFT approach was used to analyze two non-magnetic monosulfides, CaS and MgS. We determined their structural properties and then focused on the modeling of their reflectivity in the infrared region. The calculation of the reflectivity considered both harmonic and anharmonic contributions. In the harmonic limit, the non-analytic correction was employed to accurately determine the LO/TO splitting, which is necessary to delimit the retstrahlend band, that is, the maximum of the reflectivity. The anharmonic effects given by up to three-phonon and isotopic scatterings, which were included using perturbation theory, primarily smeared the reflectivity spectra edges in the high-wave region.
Secondly, four polymorphs of MnS were studied using a combination of first-principles methods to simulate their antiferromagnetic (AFM) and paramagnetic (PM) states. The integration of DFT+$U$ with special quasirandom structures (SQS) supercells, and occupation matrix control techniques was crucial for achieving convergence, structural optimization accuracy, and obtaining finite energy band gaps and local magnetic moments in the PM phases. The addition of the Hubbard $U$ correction was necessary to treat the highly-correlated Mn $d$-electrons. The success of our approach was clear based on our electronic structure predictions for the PM rock-salt B1-MnS polymorph. Experimentally this phase has been observed to be an insulator, but multiple \emph{ab initio} works resulted previously in metallic behavior. Our computations, on the other hand, predicted insulating and magnetic properties that compare well with available measurements. Additionally, the pressure-field stability of the four MnS polymorphs was studied. In the case of the PM phases, B1-MnS was identified to be the most stable up to about 21 GPa, then transforming into the B31-MnS polymorph. This finding was in close agreement with high-pressure experiments reporting a similar phase transformation. The optical properties of B1-, B4-, and B31-MnS were also simulated. The SQS technique was used to obtain soft-mode-free phonon band structures within the harmonic approximation. Then, the anharmonic effects were included, and the reflectivity was calculated for B1-MnS and B4-MnS. In both cases, a good agreement for the LO/TO splitting was achieved in comparison to experimental results.
Lastly, the oxygen-deficient heterostructure of LaAlO$_{3-\delta}$ /SrTiO$_{3-\delta}$ was investigated also employing DFT+$U$, with a particular emphasis on the potential impact of vacancy clustering at the interface. Six distinct configurations of pairs of vacancies were studied and their energies were compared to find the most stable one. The orbital reconstruction of Ti orbitals was also examined based on their location with respect to the vacancies and the local magnetic moments were calculated. The final results showed that linearly arranged vacancies located opposite to Ti ions give the most energetically stable configuration.
Auf Basis ethnographischer Feldforschung untersucht der Beitrag den Zusammenhang zwischen prekären Wohnverhältnissen und der Entstehung politischer Kollektivität unter Mieter*innen. Theoretisch-konzeptionell knüpft er dabei an Debatten der kritischen Stadtforschung zu Verdrängungsprozessen, Forschungsarbeiten zu Prekarisierung sowie poststrukturalistisch inspirierte Perspektiven der sozialen Bewegungsforschung an. Empirisch ist der Blick gerichtet auf die Lebensrealitäten von Bewohner*innen einer Frankfurter Vonovia-Wohnsiedlung. Gefragt wird danach, wie Mieter*innen ihre Wohnsituation in Anbetracht drohender Mieterhöhungen infolge von Modernisierungsarbeiten wahrnehmen, welche Bedeutung sie der Wohnungsfrage zuschreiben und welche sozialräumlichen Bedingungen, Handlungspraktiken und diskursiven Deutungsmuster die Entwicklung einer kollektiven politischen Handlungsfähigkeit erschweren.
Due to massive energetic investments in woody support structures, trees are subject to unique physiological, mechanical, and ecological pressures not experienced by herbaceous plants. Despite a wealth of studies exploring trait relationships across the entire plant kingdom, the dominant traits underpinning these unique aspects of tree form and function remain unclear. Here, by considering 18 functional traits, encompassing leaf, seed, bark, wood, crown, and root characteristics, we quantify the multidimensional relationships in tree trait expression. We find that nearly half of trait variation is captured by two axes: one reflecting leaf economics, the other reflecting tree size and competition for light. Yet these orthogonal axes reveal strong environmental convergence, exhibiting correlated responses to temperature, moisture, and elevation. By subsequently exploring multidimensional trait relationships, we show that the full dimensionality of trait space is captured by eight distinct clusters, each reflecting a unique aspect of tree form and function. Collectively, this work identifies a core set of traits needed to quantify global patterns in functional biodiversity, and it contributes to our fundamental understanding of the functioning of forests worldwide.