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Flood risk management in Europe and worldwide is not static but constantly in a state of flux. There has been a trend towards more integrated flood risk management in many countries. However, the initial situation and the pace and direction of change is very different in the various countries. In this paper, we will present a conceptual framework that seeks to explain why countries opt for different flood risk management portfolios. The developed framework utilises insights from a range of policy science concepts in an integrated way and considers, among others, factors such as geographical characteristics, the experience with flood disasters, as well as human behavioural aspects.
Uplift of the Al Hajar Mountains in Oman has been related to either Late Cretaceous ophiolite obduction or the Neogene Zagros collision. To test these hypotheses, the cooling of the central Al Hajar Mountains is constrained by 10 apatite (U-Th)/He (AHe), 15 fission track (AFT), and four zircon (U-Th)/He (ZHe) sample ages. These data show differential cooling between the two major structural culminations of the mountains. In the 3km high Jabal Akhdar culmination AHe single-grain ages range between 392 Ma and 101 Ma (2 sigma errors), AFT ages range from 518 Ma to 324 Ma, and ZHe single-grain ages range from 62 +/- 3Ma to 39 +/- 2 Ma. In the 2 km high Saih Hatat culmination AHe ages range from 26 +/- 4 to 12 +/- 4 Ma, AFT ages from 73 +/- 19Ma to 57 +/- 8 Ma, and ZHe single-grain ages from 81 +/- 4 Ma to 58 +/- 3 Ma. Thermal modeling demonstrates that cooling associated with uplift and erosion initiated at 40 Ma, indicating that uplift occurred 30 Myr after ophiolite obduction and at least 10 Myr before the Zagros collision. Therefore, this uplift cannot be related to either event. We propose that crustal thickening supporting the topography of the Al Hajar Mountains was caused by a slowdown of Makran subduction and that north Oman took up the residual fraction of N-S convergence between Arabia and Eurasia.
Bumps in river profiles: uncertainty assessment and smoothing using quantile regression techniques
(2017)
The analysis of longitudinal river profiles is an important tool for studying landscape evolution. However, characterizing river profiles based on digital elevation models (DEMs) suffers from errors and artifacts that particularly prevail along valley bottoms. The aim of this study is to characterize uncertainties that arise from the analysis of river profiles derived from different, near-globally available DEMs. We devised new algorithms quantile carving and the CRS algorithm - that rely on quantile regression to enable hydrological correction and the uncertainty quantification of river profiles. We find that globally available DEMs commonly overestimate river elevations in steep topography. The distributions of elevation errors become increasingly wider and right skewed if adjacent hillslope gradients are steep. Our analysis indicates that the AW3D DEM has the highest precision and lowest bias for the analysis of river profiles in mountainous topography. The new 12m resolution TanDEM-X DEM has a very low precision, most likely due to the combined effect of steep valley walls and the presence of water surfaces in valley bottoms. Compared to the conventional approaches of carving and filling, we find that our new approach is able to reduce the elevation bias and errors in longitudinal river profiles.
Pollen-based quantitative reconstructions of past climate variables is a standard palaeoclimatic approach. Despite knowing that the spatial extent of the calibration-set affects the reconstruction result, guidance is lacking as to how to determine a suitable spatial extent of the pollen-climate calibration-set. In this study, past mean annual precipitation (P-ann) during the Holocene (since 11.5 cal ka BP) is reconstructed repeatedly for pollen records from Qinghai Lake (36.7 degrees N, 100.5 degrees E; north-east Tibetan Plateau), Gonghai Lake (38.9 degrees N, 112.2 degrees E; north China) and Sihailongwan Lake (42.3 degrees N, 126.6 degrees E; north-east China) using calibration-sets of varying spatial extents extracted from the modern pollen dataset of China and Mongolia (2559 sampling sites and 168 pollen taxa in total). Results indicate that the spatial extent of the calibration-set has a strong impact on model performance, analogue quality and reconstruction diagnostics (absolute value, range, trend, optimum). Generally, these effects are stronger with the modern analogue technique (MAT) than with weighted averaging partial least squares (WA-PLS). With respect to fossil spectra from northern China, the spatial extent of calibration-sets should be restricted to radii between ca. 1000 and 1500 km because small-scale calibration-sets (<800 km radius) will likely fail to include enough spatial variation in the modern pollen assemblages to reflect the temporal range shifts during the Holocene, while too broad a scale calibration-set (>1500 km radius) will include taxa with very different pollen-climate relationships. (C) 2017 Elsevier Ltd. All rights reserved.
The strength of the North Atlantic Oscillation (NAO) is considered to be the main driver of climate changes over the European and western Asian continents throughout the last millennium. For example, the predominantly warm Medieval Climate Anomaly (MCA) and the following cold period of the Little Ice Age (LIA) over Europe have been associated with long-lasting phases with a positive and negative NAO index. Its climatic imprint is especially pronounced in European winter seasons. However, little is known about the influence of NAO with respect to its eastern extent over the Eurasian continent. Here we present speleothem records (PC, 8180 and Sr/Ca) from the southern rim of Fergana Basin (Central Asia) revealing annually resolved past climate variations during the last millennium. The age control of the stalagmite relies on radiocarbon dating as large amounts of detrital material inhibit accurate 230Th dating. Present-day calcification of the stalagmite is most effective during spring when the cave atmosphere and elevated water supply by snow melting and high amount of spring precipitation provide optimal conditions. Seasonal precipitation variations cause changes of the stable isotope and Sr/ Ca compositions. The simultaneous changes in these geochemical proxies, however, give also evidence for fractionation processes in the cave. By disentangling both processes, we demonstrate that the amount of winter precipitation during the MCA was generally higher than during the LIA, which is in line with climatic changes linked to the NAO index but opposite to the higher mountain records of Central Asia. Several events of strongly reduced winter precipitation are observed during the LIA in Central Asia. These dry winter events can be related to phases of a strong negative NAO index and all results reveal that winter precipitation over the central Eurasian continent is tightly linked to atmospheric NAO modes by the westerly wind systems. (C) 2017 Elsevier Ltd. All rights reserved.
We present a study of the local atomic environment of the oxygen atoms in the aqueous solutions of NaOH and HCl under simultaneous high-temperature and high-pressure conditions. Experimental nonresonant X-ray Raman scattering core-level spectra at the oxygen K-edge show systematic changes as a function of temperature and pressure. These systematic changes are distinct for the two different solutes and are described well by calculations within the Bethe- Salpeter formalism for snapshots from ab initio molecular dynamics simulations. The agreement between experimental and simulation results allows us to use the computations for a detailed fingerprinting analysis in an effort to elucidate the local atomic structure and hydrogen-bonding topology in these relevant solutions. We observe that both electrolytes, especially NaOH, enhance hydrogen bonding and tetrahedrality in the water structure at supercritical conditions, in particular in the vicinity of the hydration shells. This effect is accompanied with the association of the HCl and NaOH molecules at elevated temperatures.
Six N-alkylpyridinium salts [CnPy](2)[MCl4] (n = 4 or 12 and M = Co, Cu, Zn) were synthesized, and their structure and thermal properties were studied. The [C4Py](2)[MCl4] compounds are monoclinic and crystallize in the space group P2(1)/n. The crystals of the longer chain analogues [C12Py](2)[MCl4] are triclinic and crystallize in the space group P (1) over bar. Above the melting temperature, all compounds are ionic liquids (ILs). The derivatives with the longer C12 chain exhibit liquid crystallinity and the shorter chain compounds only show a melting transition. Consistent with single-crystal analysis, electron paramagnetic resonance spectroscopy suggests that the [CuCl4](2-) ions in the Cu-based ILs have a distorted tetrahedral geometry.
Six N-alkylpyridinium salts [CnPy](2)[MCl4] (n = 4 or 12 and M = Co, Cu, Zn) were synthesized, and their structure and thermal properties were studied. The [C4Py](2)[MCl4] compounds are monoclinic and crystallize in the space group P2(1)/n. The crystals of the longer chain analogues [C12Py](2)[MCl4] are triclinic and crystallize in the space group P (1) over bar. Above the melting temperature, all compounds are ionic liquids (ILs). The derivatives with the longer C12 chain exhibit liquid crystallinity and the shorter chain compounds only show a melting transition. Consistent with single-crystal analysis, electron paramagnetic resonance spectroscopy suggests that the [CuCl4](2-) ions in the Cu-based ILs have a distorted tetrahedral geometry.