Seismites in the Dasheng Group: New evidence of strong tectonic and earthquake activities of the Tanlu Fault Zone

More than 80 layers of seismites were recognized from the Early Cretaceous Dasheng Group in the Mazhan and Tancheng graben basins in the Tanlu Fault Zone, eastern China. The responsible seismic events took place about 110–100 Ma in the Early Cretaceous. The fault zone was affected at the time by strong tectonics, due to tension-related stretching and scattered squeezing by strike-slip faults. These tectonic activities induced a series of strong earthquakes with Richter magnitudes(M) of 5–8.5. The earthquakes affected saturated or semi-consolidated flood and lake sediments, and produced intra-layer deformations by several processes, including liquefaction, thixotropy, drop, faulting, cracking, filling and folding, which resulted in the formation of various soft-sediment deformation structures, such as dikes and veins of liquefied sand, liquefied breccias, liquefied homogeneous layers, load structures, flame structures, ball-and-pillow structures, boudinage, diapirs, fissure infillings, a giant conglomerate wedge, and syn-sedimentary faults. The seismites are new evidence of tectonic and seismic activities in the Tanlu Fault Zone during the Early Cretaceous; the series of strong seismic events that can be deduced from them must be considered as a response to the destruction of the North China Craton.     

Determination of magnitude by use of seismographs recording ground velocity

Summary Two electromagnetic seismographs HSJ-I, which are coupled with short-period galvanometers, record the velocity of the ground motion in the range of periods from 0.3 to 20 s in the seismological station Moxa. In this way the magnitude of an earthquake can be calculated without respect to the period of the ground motion. The results of such a determination of magnitudes are compared with those reached in the usual manner from short and long-period seismographs recording the ground displacement.Publication No. 45 of the Institut für Geodynamik, 69 Jena (DDR), Burgweg 11, der Deutschen Akademie der Wissenschaften zu Berlin, Forschungsgemeinschaft. Presented at the IUGG-Assembly, Zurich 1967.     

Chemical and isotopic equilibrium between CO2 and CH4 in fumarolic gas discharges: Generation of CH4 in arc magmatic-hydrothermal systems

The chemical and isotopic composition of fumarolic gases emitted from Nisyros Volcano, Greece, and of a single gas sample from Vesuvio, Italy, was investigated in order to determine the origin of methane (CH₄) within two subduction-related magmatic-hydrothermal environments.Apparent temperatures derived from carbon isotope partitioning between CH₄ and CO₂ of around 340°C for Nisyros and 470°C for Vesuvio correlate well with aquifer temperatures as measured directly and/or inferred from compositional data using the H₂O-H₂-CO₂-CO-CH₄ geothermometer. Thermodynamic modeling reveals chemical equilibrium between CH₄, CO₂ and H₂O implying that carbon isotope partitioning between CO₂ and CH₄ in both systems is controlled by aquifer temperature.N₂/³He and CH₄/³He ratios of Nisyros fumarolic gases are unusually low for subduction zone gases and correspond to those of midoceanic ridge environments. Accordingly, CH₄ may have been primarily generated through the reduction of CO₂ by H₂ in the absence of any organic matter following a Fischer-Tropsch-type reaction. However, primary occurrence of minor amounts of thermogenic CH₄ and subsequent re-equilibration with co-existing CO₂ cannot be ruled out entirely. CO₂/³He ratios and δ¹³C_CO2 values imply that the evolved CO₂ either derives from a metasomatized mantle or is a mixture between two components, one outgassing from an unaltered mantle and the other released by thermal breakdown of marine carbonates. The latter may contain traces of organic matter possibly decomposing to CH₄ during thermometamorphism.     

Zircon fission‐track ages from Newfoundland—A proxy for high geothermal gradients and exhumation before opening of the Central Atlantic Ocean

Following Appalachian orogenesis, metamorphic rocks in central Newfoundland were exhumed and reburied under Tournaisian strata. New zircon fission‐track (ZFT) ages of metamorphic rocks below the Tournaisian unconformity yield post‐depositionally reset ages of 212–235 Ma indicating regional fluid‐absent reheating to at least ≥220°C. Post‐Tournaisian sedimentary thicknesses in surrounding basins show that burial alone cannot explain such temperatures, thus requiring that palaeo‐geothermal gradients increased to ≥30–40°C/km before final late Triassic accelerated cooling. We attribute these elevated palaeo‐geothermal gradients to localized thermal blanketing by insulating sediments overlying radiogenic high‐heat‐producing granitoids. Late Triassic rifting and magmatism before break up of Pangaea likely also contributed to elevated heat flow, as well as uplift, triggering late Triassic accelerated cooling and exhumation. Thermochronological ages of 240–200 Ma are seen throughout Atlantic Canada, and record rifting and basaltic magmatism on the conjugate margins of the Central Atlantic Ocean preceding the onset of oceanic spreading at ~190 Ma.     

Stress anisotropy in natural debris flows during impacting a monitoring structure

Landslides - The frictional resistance of rock and debris is supposed to induce stress anisotropy in the unsteady, non-uniform flow of gravitational mass flows, including debris flows. Though...     

The emergence of an ‘evolutionary geomorphology’?

Earth surface processes and landforms are modified through the actions of many microorganisms, plants and animals. As organism-driven landform modifications are sometimes to the advantage of the organism, some of these landform features have become adaptive functional components of ecosystems, concurrently affecting and responding to ecological and evolutionary processes. These recent eco-evolutionary insights, focused on feedback among geomorphologic, ecological and evolutionary processes, are currently leading to the emergence of what has been called an ??evolutionary geomorphology??, with explicit consideration of feedbacks among the evolution of organisms, ecosystem structure and function and landform organization at the Earth surface. Here we provide an overview in the form of a commentary of this emerging sub-discipline in geosciences and ask whether the use of the term ??evolutionary geomorphology?? is appropriate or rather misleading.     

Ternary feldspars: Kinetics and possible equilibria at 800° C

The ternary feldspar system KAlSi₃O₈ - NaAlSi₃O₈ - CaAl₂Si₂O₈ was reinvestigated at 650 ° C and 800 ° C (P _H2O = 1 kb) using mixtures of crystalline plagioclases and alkali feldspars as starting materials. The compositions of plagioclases and alkali feldspars of the run products were determined by X-ray means. The Or-content of the feldspar phases was determined by measuring the position of the (201) X-ray peak of the unexchanged feldspars, whereas the An-content was determined by measuring the same X-ray peak of the K-exchanged feldspars. The reaction rate of a reaction leading to a more An-rich plagioclase (type II reaction) is much faster than a reaction producing a more Ab-rich plagioclase (type I). In a type II reaction run times of approximately 20 days are needed to reach new constant plagioclase and alkali feldspar compositions at 650 ° C, and 10 days are needed to reach constant compositions at 800 ° C. In a reaction of type I only the outer zone of the plagioclases reacts to more Abrich compositions. A diffuse zone with a wide range of compositions was observed in 650 ° C runs. Equilibrium could not be reached in these experiments within 45 days. At 800 ° C a new zone having a specific composition develops in 42 days. This new zone is believed to be in equilibrium with the coexisting alkali feldspar. The depth of reaction is calculated as 0.03 μm after 42 days (800 ° C, P _f= 1 kb). The reaction between the two feldspar phases could be reversed at 800 ° C. The following compositions are considered to represent equilibrium data at 800 ° C and P _t = 1 kb:

An 43 Ab 51 Or 6 coexisting with Or 79 Ab 20 An 1, and

An 40 Ab 54 Or 6 coexisting with Or 75 Ab 24 An 1.

Recent data obtained with gels of ternary feldspar composition as starting materials do not agree with the results presented in this paper. Gels obviously crystallize spontaneously forming coexisting feldspars of non - equilibrium composition - alkali feldspars too rich in Ab and plagioclases too rich in An.     

Nitrogen isotopes in the solar system

Measurements of the isotopic composition of nitrogen in the solar system are summarized. We show that the 30% change, during the last 3 to 4 billion years, of ${}^{15}\text{N}{}^{14}\text{N}$ in solar-wind-bearing lunar soils and breccias probably does not reflect changes in this ratio at the solar surface. Such changes, whether by spallation or thermonuclear reactions are ruled out by comparing the yields of ¹⁵N with those of other rare isotopes such as ⁹Be, ¹¹B, ³He or ¹³C, even if an arbitrary degree of solar mixing is introduced. Moreover, we calculate that the solar activity required for producing significant amounts of ¹⁵N by spallation at the solar surface should have resulted in a particle bombardment of the Moon of an intensity that would have produced amounts of spallation isotopes (e.g.¹⁵N, ²¹Ne, ³⁸Ar, ¹³¹Xe) several orders of magnitude in excess of what is actually found in the whole regolith.We argue that accretion of interstellar matter also does not work as a cause for a significant change of the photospheric ${}^{15}\text{N}{}^{14}\text{N}$ ratio. Evidence is presented that the mixing depth at the solar surface on a time scale of ?10⁹ years is (10^?2 ?10^?1) M_⊙ Mixing to this depth renders accretion of interstellar matter as a source of compositional changes at the solar surface inefficient, even if allowance is made for the expected large difference in the accretion rates of condensed and gaseous matter. A quantitative treatment of several alternatives of solar accretion leads to serious contradictions (e.g. with the low Ne abundances in planetary atmospheres or with the amounts of nitrogen that should have been directly accreted by the Moon), and we conclude that accretion during the main sequence life of the Sun is an unlikely source of changes in ${}^{15}\text{N}{}^{14}\text{N}$ at the solar surface.A ratio of ${}^{15}\text{N}{}^{14}\text{N}\text{= (4.0 ± 0.3) × 10}{}^{\mathrm{?3}}$ is our best estimate for average solar system material and for the Sun. We propose that a rare, very light nitrogen component (called LPN) is admixed in varying amounts to planetary matter. Undiluted LPN has not been found in meteorites or planetary atmospheres, but we show that the combined effects of LPN admixture and isotope fractionation can in principle account for the variability of ${}^{15}\text{N}{}^{14}\text{N}$ observed in the planetary system. Determination of the Jovian ${}^{15}\text{N}{}^{14}\text{N}$ ratio with an accuracy of ~10% would crucially test our interpretation of the nitrogen isotope observations.