@phdthesis{Olen2016,
  author    = {Olen, Stephanie M.},
  title     = {Understanding Himalayan denudation at the catchment and orogen scale},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-91423},
  school      = {Universit{\"a}t Potsdam},
  pages     = {xx, 174},
  year      = {2016},
  abstract  = {Understanding the rates and processes of denudation is key to unraveling the dynamic processes that shape active orogens. This includes decoding the roles of tectonic and climate-driven processes in the long-term evolution of high- mountain landscapes in regions with pronounced tectonic activity and steep climatic and surface-process gradients. Well-constrained denudation rates can be used to address a wide range of geologic problems. In steady-state landscapes, denudation rates are argued to be proportional to tectonic or isostatic uplift rates and provide valuable insight into the tectonic regimes underlying surface denudation. The use of denudation rates based on terrestrial cosmogenic nuclide (TCN) such as 10Beryllium has become a widely-used method to quantify catchment-mean denudation rates. Because such measurements are averaged over timescales of 102 to 105 years, they are not as susceptible to stochastic changes as shorter-term denudation rate estimates (e.g., from suspended sediment measurements) and are therefore considered more reliable for a comparison to long-term processes that operate on geologic timescales. However, the impact of various climatic, biotic, and surface processes on 10Be concentrations and the resultant denudation rates remains unclear and is subject to ongoing discussion. In this thesis, I explore the interaction of climate, the biosphere, topography, and geology in forcing and modulating denudation rates on catchment to orogen scales. There are many processes in highly dynamic active orogens that may effect 10Be concentrations in modern river sands and therefore impact 10Be-derived denudation rates. The calculation of denudation rates from 10Be concentrations, however, requires a suite of simplifying assumptions that may not be valid or applicable in many orogens. I investigate how these processes affect 10Be concentrations in the Arun Valley of Eastern Nepal using 34 new 10Be measurements from the main stem Arun River and its tributaries. The Arun Valley is characterized by steep gradients in climate and topography, with elevations ranging from <100 m asl in the foreland basin to >8,000 asl in the high sectors to the north. This is coupled with a five-fold increase in mean annual rainfall across strike of the orogen. Denudation rates from tributary samples increase toward the core of the orogen, from <0.2 to >5 mm/yr from the Lesser to Higher Himalaya. Very high denudation rates (>2 mm/yr), however, are likely the result of 10Be TCN dilution by surface and climatic processes, such as large landsliding and glaciation, and thus may not be representative of long-term denudation rates. Mainstem Arun denudation rates increase downstream from ~0.2 mm/yr at the border with Tibet to 0.91 mm/yr at its outlet into the Sapt Kosi. However, the downstream 10Be concentrations may not be representative of the entire upstream catchment. Instead, I document evidence for downstream fining of grains from the Tibetan Plateau, resulting in an order-of-magnitude apparent decrease in the measured 10Be concentration. In the Arun Valley and across the Himalaya, topography, climate, and vegetation are strongly interrelated. The observed increase in denudation rates at the transition from the Lesser to Higher Himalaya corresponds to abrupt increases in elevation, hillslope gradient, and mean annual rainfall. Thus, across strike (N-S), it is difficult to decipher the potential impacts of climate and vegetation cover on denudation rates. To further evaluate these relationships I instead took advantage of an along-strike west-to-east increase of mean annual rainfall and vegetation density in the Himalaya. An analysis of 136 published 10Be denudation rates from along strike of the revealed that median denudation rates do not vary considerably along strike of the Himalaya, ~1500 km E-W. However, the range of denudation rates generally decreases from west to east, with more variable denudation rates in the northwestern regions of the orogen than in the eastern regions. This denudation rate variability decreases as vegetation density increases (R=- 0.90), and increases proportionately to the annual seasonality of vegetation (R=0.99). Moreover, rainfall and vegetation modulate the relationship between topographic steepness and denudation rates such that in the wet, densely vegetated regions of the Himalaya, topography responds more linearly to changes in denudation rates than in dry, sparsely vegetated regions, where the response of topographic steepness to denudation rates is highly nonlinear. Understanding the relationships between denudation rates, topography, and climate is also critical for interpreting sedimentary archives. However, there is a lack of understanding of how terrestrial organic matter is transported out of orogens and into sedimentary archives. Plant wax lipid biomarkers derived from terrestrial and marine sedimentary records are commonly used as paleo- hydrologic proxy to help elucidate these problems. I address the issue of how to interpret the biomarker record by using the plant wax isotopic composition of modern suspended and riverbank organic matter to identify and quantify organic matter source regions in the Arun Valley. Topographic and geomorphic analysis, provided by the 10Be catchment-mean denudation rates, reveals that a combination of topographic steepness (as a proxy for denudation) and vegetation density is required to capture organic matter sourcing in the Arun River. My studies highlight the importance of a rigorous and careful interpretation of denudation rates in tectonically active orogens that are furthermore characterized by strong climatic and biotic gradients. Unambiguous information about these issues is critical for correctly decoding and interpreting the possible tectonic and climatic forces that drive erosion and denudation, and the manifestation of the erosion products in sedimentary archives.},
  language  = {en}
}
@phdthesis{KonradSchmolke2016,
  author    = {Konrad-Schmolke, Matthias},
  title     = {Thermodynamic and geochemical modeling in metamorphic geology},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-101805},
  school      = {Universit{\"a}t Potsdam},
  pages     = {232},
  year      = {2016},
  abstract  = {Quantitative thermodynamic and geochemical modeling is today applied in a variety of geological environments from the petrogenesis of igneous rocks to the oceanic realm. Thermodynamic calculations are used, for example, to get better insight into lithosphere dynamics, to constrain melting processes in crust and mantle as well as to study fluid-rock interaction. The development of thermodynamic databases and computer programs to calculate equilibrium phase diagrams have greatly advanced our ability to model geodynamic processes from subduction to orogenesis. However, a well-known problem is that despite its broad application the use and interpretation of thermodynamic models applied to natural rocks is far from straightforward. For example, chemical disequilibrium and/or unknown rock properties, such as fluid activities, complicate the application of equilibrium thermodynamics. One major aspect of the publications presented in this Habilitationsschrift are new approaches to unravel dynamic and chemical histories of rocks that include applications to chemically open system behaviour. This approach is especially important in rocks that are affected by element fractionation due to fractional crystallisation and fluid loss during dehydration reactions. Furthermore, chemically open system behaviour has also to be considered for studying fluid-rock interaction processes and for extracting information from compositionally zoned metamorphic minerals. In this Habilitationsschrift several publications are presented where I incorporate such open system behaviour in the forward models by incrementing the calculations and considering changing reacting rock compositions during metamorphism. I apply thermodynamic forward modelling incorporating the effects of element fractionation in a variety of geodynamic and geochemical applications in order to better understand lithosphere dynamics and mass transfer in solid rocks. In three of the presented publications I combine thermodynamic forward models with trace element calculations in order to enlarge the application of geochemical numerical forward modeling. In these publications a combination of thermodynamic and trace element forward modeling is used to study and quantify processes in metamorphic petrology at spatial scales from µm to km. In the thermodynamic forward models I utilize Gibbs energy minimization to quantify mineralogical changes along a reaction path of a chemically open fluid/rock system. These results are combined with mass balanced trace element calculations to determine the trace element distribution between rock and melt/fluid during the metamorphic evolution. Thus, effects of mineral reactions, fluid-rock interaction and element transport in metamorphic rocks on the trace element and isotopic composition of minerals, rocks and percolating fluids or melts can be predicted. One of the included publications shows that trace element growth zonations in metamorphic garnet porphyroblasts can be used to get crucial information about the reaction path of the investigated sample. In order to interpret the major and trace element distribution and zoning patterns in terms of the reaction history of the samples, we combined thermodynamic forward models with mass-balance rare earth element calculations. Such combined thermodynamic and mass-balance calculations of the rare earth element distribution among the modelled stable phases yielded characteristic zonation patterns in garnet that closely resemble those in the natural samples. We can show in that paper that garnet growth and trace element incorporation occurred in near thermodynamic equilibrium with matrix phases during subduction and that the rare earth element patterns in garnet exhibit distinct enrichment zones that fingerprint the minerals involved in the garnet-forming reactions. In two of the presented publications I illustrate the capacities of combined thermodynamic-geochemical modeling based on examples relevant to mass transfer in subduction zones. The first example focuses on fluid-rock interaction in and around a blueschist-facies shear zone in felsic gneisses, where fluid-induced mineral reactions and their effects on boron (B) concentrations and isotopic compositions in white mica are modeled. In the second example, fluid release from a subducted slab and associated transport of B and variations in B concentrations and isotopic compositions in liberated fluids and residual rocks are modeled. I show that, combined with experimental data on elemental partitioning and isotopic fractionation, thermodynamic forward modeling unfolds enormous capacities that are far from exhausted. In my publications presented in this Habilitationsschrift I compare the modeled results to geochemical data of natural minerals and rocks and demonstrate that the combination of thermodynamic and geochemical models enables quantification of metamorphic processes and insights into element cycling that would have been unattainable so far. Thus, the contributions to the science community presented in this Habilitatonsschrift concern the fields of petrology, geochemistry, geochronology but also ore geology that all use thermodynamic and geochemical models to solve various problems related to geo-materials.},
  language  = {en}
}