scholarly journals Relocated Hypocenters and Structural Analysis from Waveform Modeling of Aftershocks from the 2011 Prague, Oklahoma, Earthquake Sequence

2017 ◽  
Vol 107 (2) ◽  
pp. 553-562 ◽  
Author(s):  
Marius P. Isken ◽  
Walter D. Mooney
1999 ◽  
Vol 89 (4) ◽  
pp. 1094-1108 ◽  
Author(s):  
Douglas Dreger ◽  
Brian Savage

Abstract We have studied the seismograms recorded at the historic Berkeley (BRK) and Pasadena (PAS) stations for 20 aftershocks of the 21 July 1952 Kern County earthquake sequence. These events, in the magnitude range of MW 4.5 to 5.6, are too small to be studied teleseismically, yet they are important for better understanding the tectonics of the southern Sierra Nevada and the Tehachapi Mountains. On-scale recordings of moderate-sized events from this important earthquake sequence were first scanned, digitized, and then subjected to waveform modeling using a seismic moment tensor inverse procedure. In particular, the long-period, three-component Galitzen instrument at BRK and the 6-sec Wood-Anderson at PAS provided very high quality seismograms that could be analyzed in this manner. These two sites have been continuously operated from 1887 and 1927, respectively, and both are current sites of state-of-the-art broadband, high dynamic range instrumentation. First-motion polarities reported by Bath and Richter (1958) were used as additional constraints in the estimation of source parameters. There is considerable variability in the three-component seismograms of the 1952 aftershocks, which in turn result in a diversity of focal mechanisms. The majority of the solutions are northwest-striking reverse mechanisms that likely occurred on various mapped thrust faults in the hanging block of the mainshock. There are several events with northeast-striking, left-lateral mechanisms that are consistent with the strike of the White Wolf fault, as well as several normal slip events. The results of this study indicate that there are a variety of active fault structures adjacent to the White Wolf, Garlock and San Andreas faults in this region.


Author(s):  
W. H. Wu ◽  
R. M. Glaeser

Spirillum serpens possesses a surface layer protein which exhibits a regular hexagonal packing of the morphological subunits. A morphological model of the structure of the protein has been proposed at a resolution of about 25 Å, in which the morphological unit might be described as having the appearance of a flared-out, hollow cylinder with six ÅspokesÅ at the flared end. In order to understand the detailed association of the macromolecules, it is necessary to do a high resolution structural analysis. Large, single layered arrays of the surface layer protein have been obtained for this purpose by means of extensive heating in high CaCl2, a procedure derived from that of Buckmire and Murray. Low dose, low temperature electron microscopy has been applied to the large arrays.As a first step, the samples were negatively stained with neutralized phosphotungstic acid, and the specimens were imaged at 40,000 magnification by use of a high resolution cold stage on a JE0L 100B. Low dose images were recorded with exposures of 7-9 electrons/Å2. The micrographs obtained (Fig. 1) were examined by use of optical diffraction (Fig. 2) to tell what areas were especially well ordered.


Author(s):  
E. Loren Buhle ◽  
Pamela Rew ◽  
Ueli Aebi

While DNA-dependent RNA polymerase represents one of the key enzymes involved in transcription and ultimately in gene expression in procaryotic and eucaryotic cells, little progress has been made towards elucidation of its 3-D structure at the molecular level over the past few years. This is mainly because to date no 3-D crystals suitable for X-ray diffraction analysis have been obtained with this rather large (MW ~500 kd) multi-subunit (α2ββ'ζ). As an alternative, we have been trying to form ordered arrays of RNA polymerase from E. coli suitable for structural analysis in the electron microscope combined with image processing. Here we report about helical polymers induced from holoenzyme (α2ββ'ζ) at low ionic strength with 5-7 mM MnCl2 (see Fig. 1a). The presence of the ζ-subunit (MW 86 kd) is required to form these polymers, since the core enzyme (α2ββ') does fail to assemble into such structures under these conditions.


Author(s):  
Paul DeCosta ◽  
Kyugon Cho ◽  
Stephen Shemlon ◽  
Heesung Jun ◽  
Stanley M. Dunn

Introduction: The analysis and interpretation of electron micrographs of cells and tissues, often requires the accurate extraction of structural networks, which either provide immediate 2D or 3D information, or from which the desired information can be inferred. The images of these structures contain lines and/or curves whose orientation, lengths, and intersections characterize the overall network.Some examples exist of studies that have been done in the analysis of networks of natural structures. In, Sebok and Roemer determine the complexity of nerve structures in an EM formed slide. Here the number of nodes that exist in the image describes how dense nerve fibers are in a particular region of the skin. Hildith proposes a network structural analysis algorithm for the automatic classification of chromosome spreads (type, relative size and orientation).


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