Ejection behavior characteristics in experimental cratering in sandstone targets     

Frank SOMMER  Fiona REISER  Anja DUFRESNE  Michael H. POELCHAU  Tobias HOERTH  Alex DEUTSCH  Thomas KENKMANN  Klaus THOMA 《Meteoritics & planetary science》2013,48(1):33-49

Abstract– Within the frame of the MEMIN research unit (Multidisciplinary Experimental and Numerical Impact Research Network), impact experiments on sandstone targets were carried out to systematically study the influence of projectile mass, velocity, and target water saturation on the cratering and ejection processes. The projectiles were accelerated with two‐stage light‐gas guns (Ernst‐Mach‐Institute) onto fine‐grained targets (Seeberger sandstone) with about 23% porosity. Collection of the ejecta on custom‐designed catchers allowed determination of particle shape, size distribution, ejection angle, and microstructures. Mapping of the ejecta imprints on the catcher surface enabled linking of the different patterns to ejection stages observed on high‐speed videos. The increase in projectile mass from 0.067 to 7.1 g correlates with an increase in the total ejected mass; ejecta angles, however, are similar in range for all experiments. The increase in projectile velocity from 2.5 to 5.1 km s^?1 correlates with a total ejecta mass increase as well as in an increase in comminution efficiency, and a widening of the ejecta cone. A higher degree of water saturation of the target yields an increase in total ejecta mass up to 400% with respect to dry targets, higher ejecta velocity, and a steeper cone. These data, in turn, suggest that the reduced impedance contrast between the quartz grains of the target and the pores plays a primary role in the ejecta mass increase, while vaporization of water determines the ejecta behavior concerning ejecta velocity and particle distribution.  相似文献   

Annual dynamics of pelagic primary production and respiration in a shallow coastal basin     

Martina Loebl  Tobias Dolch  Justus E.E. van Beusekom 《Journal of Sea Research》2007,58(4):269-282

The Wadden Sea (North Sea, Europe) is a shallow coastal sea with high benthic and pelagic primary production rates. To date, no studies have been carried out in the Wadden Sea that were specifically designed to study the relation between pelagic respiration and production by comparable methods. Because previous studies have suggested that the import of primary-produced pelagic organic matter is important for benthic Wadden Sea carbon budgets, we hypothesised that on an annual average the northern Wadden Sea water column is autotrophic. To test this hypothesis, we studied annual dynamics of primary production and respiration at a pelagic station in a shallow tidal basin (List Tidal Basin, northern Wadden Sea). Since water depth strongly influences production estimates, we calculated primary production rates per unit area in two ways: on the basis of the mean water depth (2.7 m) and on the basis of 1 m depth intervals and their respective spatial extent in the List Tidal Basin. The latter more precise estimate yielded an annual primary production of 146 g C m^− 2 y^− 1. Estimates based on the mean water depth resulted in a 40% higher annual rate of 204 g C m^− 2 y^− 1. The total annual pelagic respiration was 50 g C m^− 2 y^− 1. The P/R ratio varied between seasons: from February to October the water column was autotrophic, with the highest P/R ratio of 4–5 during the diatom spring bloom in April/May. In autumn and winter the water column was heterotrophic. On an annual average, the water column of the List Tidal Basin was autotrophic (P/R 3). We suggest that a large fraction of the pelagic produced organic matter was respired locally in the sediment.  相似文献   

Effects of soil organic matter composition on unfrozen water content and heterotrophic CO₂ production of frozen soils     

Stina Harrysson Drotz  Tobias Sparrman  Mats Nilsson 《Geochimica et cosmochimica acta》2010,74(8):2281-2290

Several recent studies have highlighted the importance of soil organic matter (SOM) mineralization at high latitudes during winter for ecosystem carbon (C) balances, and the ability of the soil to retain unfrozen water at sub-zero temperatures has been shown to be a major determinant of C mineralization rates. Further, SOM is believed to strongly influence the liquid water contents in frozen surface layers of boreal forest soils and tundra, but the mechanisms and specific factors involved are currently unknown. Here we evaluate the effects of the chemical composition of SOM on the amount of unfrozen water, the pore size equivalents in which unfrozen water can exist, and the microbial heterotrophic activity at sub-zero temperatures in boreal forest soils. To do this, we have characterized the chemical composition of SOM in forest soil samples (surface O-horizons) using solid state CP-MAS (cross polarization magic angle spinning) NMR spectroscopy. The acquired information was then used to elucidate the extent to which different fractions of SOM can explain the observed variations in unfrozen water content, pore size equivalents, and biogenic CO₂ production rates in the examined soil samples under frozen conditions (−4 °C). The data evaluation was done by the use of principal component analysis (PCA) and projections to latent structures by means of partial least square (PLS). We conclude that aromatic, O-aromatic, methoxy/N-alkyl and alkyl C are the major SOM components affecting frozen boreal forest soil’s ability to retain unfrozen water and sustain heterotrophic activity (95% confidence level). Our results reveal that solid carbohydrates have a significant negative impact (95% confidence level) on CO₂ production in frozen boreal spruce forest soils, in contrast to the positive effects of carbohydrate polymers during unfrozen conditions. We conclude that the hierarchy of environmental factors controlling SOM mineralization changes as soils freeze. The effect of SOM composition on pore size distribution and unfrozen water content has a superior influence on SOM mineralization and hence on heterotrophic CO₂ production of frozen soils.  相似文献   

The biogeochemistry of sorbed methane in marine sediments     

Tobias F. Ertefai  Verena B. Heuer  Christoph Vogt  Jeffrey Seewald 《Geochimica et cosmochimica acta》2010,74(21):6033-6048

Sorption of volatile hydrocarbon gases (VHCs) to marine sediments is a recognized phenomenon that has been investigated in the context of petroleum exploration. However, little is known about the biogeochemistry of sorbed methane and higher VHCs in environments that are not influenced by thermogenic processes. This study evaluated two different extraction protocols for sorbed VHCs, used high pressure equipment to investigate the sorption of methane to pure clay mineral phases, and conducted a geochemical and mineralogical survey of sediment samples from different oceanographic settings and geochemical regimes that are not significantly influenced by thermogenic gas. Extraction of sediments under alkaline conditions yielded higher concentrations of sorbed methane than the established protocol for acidic extraction. Application of alkaline extraction in the environmental survey revealed the presence of substantial amounts of sorbed methane in 374 out of 411 samples (91%). Particularly high amounts, up to 2.1 mmol kg⁻¹ dry sediment, were recovered from methanogenic sediments. Carbon isotopic compositions of sorbed methane suggested substantial contributions from biogenic sources, both in sulfate-depleted and sulfate-reducing sediments. Carbon isotopic relationships between sorbed and dissolved methane indicate a coupling of the two pools. While our sorption experiments and extraction conditions point to an important role for clay minerals as sorbents, mineralogical analyses of marine sediments suggest that variations in mineral composition are not controlling variations in quantities of sorbed methane. We conclude that the distribution of sorbed methane in sediments is strongly influenced by in situ production.  相似文献   

Slip rate variations on faults in the Basin-and-Range Province caused by regression of Late Pleistocene Lake Bonneville and Lake Lahontan     

Tobias Karow  Andrea Hampel 《International Journal of Earth Sciences》2010,99(8):1941-1953

Late Pleistocene regression of two large pluvial lakes—Lake Bonneville and Lake Lahontan—caused considerable lithospheric rebound in the Basin-and-Range Province, USA. Here, we use finite-element models to show how lake growth and regression affect the temporal and spatial slip evolution on faults near the former lakes. Our results show that fluctuations in the volume of Lake Bonneville caused along-strike slip variations on the Wasatch normal fault, with a pronounced slip rate increase on its northern and central parts during lake regression. The response of normal and strike-slip faults near the ring-shaped Lake Lahontan depends on their location within the rebound area. Faults located in the centre of rebound show a slip rate increase during lake regression, whereas strike-slip faults at the periphery decelerate. All slip rate variations are caused by differential stress changes owing to changing lake levels, regardless of the individual fault response.  相似文献   

Isotope Geochemistry of the Pb-Zn-Ba(-Ag-Au) Mineralization at Triades-Galana,Milos Island,Greece     

Robert Marschik  Tobias Bauer  Ana-Sophie Hensler  Nikos Skarpelis  Stefan Hölzl 《Resource Geology》2010,60(4):335-347

The Pb-Zn-Ba(-Ag-Au) mineralization in the Triades and Galana mine areas is hosted in 2.5–1.4 Ma pyroclastic rocks, and structurally controlled mostly by NE-SW or N-S trending brittle faults. Proximal pervasive silica and distal pervasive sericite-illite alteration are the two main alteration types present at the surface. The distribution of mineralization-alteration in the district suggests at least two hydrothermal events or that hydrothermal activity lasted longer at Galana. The Sr isotope signature of sphalerite and barite (⁸⁷Sr/⁸⁶Sr = 0.709162 to 0.710214) and calculated oxygen isotope composition of a fluid in equilibrium with barite and associated quartz at temperatures of around 230°C are suggestive of a seawater hydrothermal system and fluid/rock interaction. Lead isotope ratios of galena and sphalerite (²⁰⁶Pb/²⁰⁴Pb from 18.8384 to 18.8711; ²⁰⁷Pb/²⁰⁴Pb from 15.6695 to 15.6976; ²⁰⁸Pb/²⁰⁴Pb from 38.9158 to 39.0161) are similar to those of South Aegean Arc volcanic and Aegean Miocene plutonic rocks, and compatible with Pb derived from an igneous source. Galena and sphalerite from Triades-Galana have δ³⁴S_VCDT values ranging from +1 to +3.6‰, whereas barite sulfate shows δ³⁴S_VCDT values from +22.8 to +24.4‰. The sulfur isotope signatures of these minerals are explained by seawater sulfate reduction processes. The new analytical data are consistent with a seawater-dominated hydrothermal system and interaction of the hydrothermal fluid with the country rocks, which are the source of the ore metals.  相似文献