An Anisotropic Cosmic-Ray Enhancement Event on 07-June-2015: A Possible Origin

A usual event, called anisotropic cosmic-ray enhancement (ACRE), was observed as a small increase (\({\leq}\,5\%\)) in the count rates of polar neutron monitors during 12?–?19 UT on 07 June 2015. The enhancement was highly anisotropic, as detected only by neutron monitors with asymptotic directions in the southwest quadrant in geocentric solar ecliptic (GSE) coordinates. The estimated rigidity of the corresponding particles is \({\leq}\,1\) GV. No associated detectable increase was found in the space-borne data from the Geostationary Operational Environmental Satellite (GOES), the Energetic and Relativistic Nuclei and Electron (ERNE) on board the Solar and Heliospheric Observatory (SOHO), or the Payload for Antimatter Matter Exploration and Light-nuclei Astrophysics (PAMELA) instruments, whose sensitivity was not sufficient to detect the event. No solar energetic particles were present during that time interval. The heliospheric conditions were slightly disturbed, so that the interplanetary magnetic field strength gradually increased during the event, followed by an increase of the solar wind speed after the event. It is proposed that the event was related to a crossing of the boundary layer between two regions with different heliospheric parameters, with a strong gradient of low-rigidity (\({<}\,1\) GV) particles. It was apparently similar to another cosmic-ray enhancement (e.g., on 22 June 2015) that is thought to have been caused by the local anisotropy of Forbush decreases, with the difference that in our case, the interplanetary disturbance was not observed at Earth, but passed by southward for this event.     

Beitrag zur quantitativen Analyse von Mineralphasen mittels Röntgendiffraktion

Zusammenfassung Bei der Durchführung quantitativer Gemenge-Analysen mit Hilfe der Röntgendiffraktionsmethode kann man den Massenschwächungskoeffizienten (^*) verwenden, den man bei der Röntgenfluoreszenzanalyse Röhrenhauptlinienverfahren vonSchroll-Stepon erhalten hat. Er wird von der Wellenlänge der Röntgenfluoreszenzstreustrahlung auf die Wellenlänge der Diffraktionsröhre transformiert. Ein Intensitäts-Konzentrationsdiagramm, in dem die Intensität der gewählten Diffraktionslinie durch das Produkt von Intensität und dem jeweiligen Wert von ^* ersetzt wird, ergibt eine allgemeingültige Eichgerade. Als Beispiel werden Messungen an Zweistoffsystemen wie Magnesit-Quarz, Albit-Quarz, Calcit-Quarz, Stilpnomelan-Quarz und Siderit-Quarz angeführt.Die vorgeschlagene Methode ist für kombinierte Diffraktions- und Röntgenfluoreszenzanalysen sehr zweckmäßig.

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Summary Applicating the quantitative X-ray-diffraction-analysis für mixtures of minerals the use of the mass absorption coefficient (^*) is possible, which is received by the X-ray-fluorescence-analysis of the same sample following the method proposed by the authors. The mass absorption coefficients must be transformed to the new wave length of the X-ray-diffraction tube. In the intensity-concentration-diagram the intensity is substituted by the product of intensity and mass absorption coefficient. An uniform standard line is received, as the measurement of quartz shows in the systems of two-substances, such as magnesite-quartz, albite-quartz, calcite-quartz, stilpnomelan-quartz and siderite-quartz.The proposed method is very useful for the combined X-ray-diffraction and X-ray fluorescence analysis.

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Mit 6 Textabbildungen     

Petroleum-related hydrocarbons in deep and subsurface sediments from South-Western Barents Sea

Subsurface sediments from a pockmark area in South-Western Barents Sea have been earlier found to contain elevated levels of petroleum-related polycyclic aromatic hydrocarbons. This work describes a comprehensive analysis of various biomarkers, including the highly source-specific hopanes, in a 4.5?m long gravity core from the same area, together with subsurface sediment samples from other areas in the region without pockmarks present ("background samples"). A clear difference between the pockmark gravity core and the background sediment cores was found, both with regard to genesis and the level of transformation of organic matter. A number of indicator parameters, such as methylphenanthrene index (MPI-1), point towards a significantly higher maturity of hydrocarbons in the pockmark core throughout its length as compared to the other sampled locations. Higher contents of microbial hopanoids (hopenes) may indicate the former presence of petroleum. These findings confirm the hypothesis of a natural hydrocarbon source in the deeper strata present in the studied location with pockmarks.     

Spatial and vertical distributions of elements in sediments of the Colorado River delta and Upper Gulf of California

The abundance of major components (Fe, Ca, K, and organic carbon) and trace elements was analyzed in surface sediments and core samples from the Colorado River delta (CRD) and the Upper Gulf of California (UGC) using instrumental neutron activation analysis.The spatial distribution patterns of the elements studied are consistent with the model of sedimentary dynamics proposed for this area [Mar. Geol. 158 (1999) 125]: intense tidal resuspension of sediments in the delta with subsequent transport of suspended particulate matter in a southerly direction, followed by sedimentation of fine-grained material in a depocenter near the southwestern margin of the UGC. Concentrations of most of the elements are higher in the surface sediments of this depocenter. The gradual mixing of terrigenous and marine biogenic materials, normally expected for the estuarine sediments, was not detected in the CRD–UGC system because of homogenization of the sediments by tides and wind.Vertical profiles of element contents in samples of the sediment core collected in the depocenter area revealed (i) almost no anthropogenic contamination of the area by environmentally important trace elements such as Cr, Co, Sb, and As; (ii) a twofold decrease of Fe, Sc, Cr, and Co in upper core sediments; and (iii) the enrichment of the sediments at 60–62 cm depth in the core, in calcium carbonate, Ca, Sr, and the Eu_n/Sm_n shale-normalized ratio along with a depletion in this layer of Fe, Sc, Cr, Co, light rare-earth elements (REEs), and some other elements of terrigenous origin, presumably caused by the dilution of fluvial terrigenous material by biogenic carbonates, which were probably introduced at this level in the sediments by the action of a strong episodic winter storm, followed by the advective transport of shell fragments from the coastal clam banks or as a result of strong planktonic bloom.     

Solar Wind Plasma Particles Organized by the Flow Speed

An understanding of solar variability over a broad spectral range and broad range of timescales is needed by scientists studying Earth’s climate. The Total and Spectral Solar Irradiance Sensor (TSIS) Spectral Irradiance Monitor (SIM), is designed to measure solar spectral irradiance (SSI) with unprecedented accuracy from 200 nm to 2400 nm. SIM started daily observations in March 2018. To maintain its accuracy over the course of its anticipated 5-year mission and beyond, TSIS SIM needs to be corrected for optical degradation, common for solar viewing instruments. The differing long-term trends of various independent solar-irradiance records attest to the challenge at hand.

The correction of TSIS SIM for optical degradation is based on piecewise linear fits that bring the three instrument channels into agreement. It is fundamentally different to the correction applied to the TSIS SIM predecessor on SORCE. The correction facilitates reproducibility, uncertainty estimation and is measurement-based. Corrected, integrated TSIS SIM SSI agrees with independent observations of total solar irradiance to within 45 ppm as well as various solar-irradiance models. TSIS SIM SSI is available at: http://lasp.colorado.edu/lisird/.

     

Using multiple-accumulator CMACs to improve efficiency of the X part of an input-buffered FX correlator

This paper presents the approach of using complex multiplier-accumulators (CMACs) with multiple accumulators to reduce the total number of memory operations in an input-buffered architecture for the X part of an FX correlator. A processing unit of this architecture uses an array of CMACs that are reused for different groups of baselines. The disadvantage of processing correlations in this way is that each input data sample has to be read multiple times from the memory because each input signal is used in many of these baseline groups. While a one-accumulator CMAC cannot switch to a different baseline until it is finished integrating the current one, a multiple-accumulator CMAC can. Thus, the array of multiple-accumulator CMACs can switch between processing different baselines that share some input signals at any moment to reuse the current data in the processing buffers. In this way significant reductions in the number of memory read operations are achieved with only a few accumulators per CMAC. For example, for a large number of input signals three-accumulator CMACs reduce the total number of memory operations by more than a third. Simulated energy measurements of four VLSI designs in a high-performance 28 nm CMOS technology are presented in this paper to demonstrate that using multiple accumulators can also lead to reduced power dissipation of the processing array. Using three accumulators as opposed to one has been found to reduce the overall energy of 8-bit CMACs by 1.4% through the reduction of the switching activity within their circuits, which is in addition to a more than 30% reduction in the memory.     

Identification of estrogen-like alkylphenols in produced water from offshore oil installations

Produced water released into the sea from oil installations contains a vast number of organic compounds. This work focuses on the analysis and identification of phenols in produced water, in particular long-chain para-substituted alkylphenols, which act as endocrine disruptors for marine biota. Some alkylphenol standards, unavailable commercially, have been synthesised and some compounds of interest identified. However, a complete identification is not possible since conventional GC techniques cannot achieve the desired degree of separation. An overview of the levels of the 52 known alkylphenols in produced water from nine oil installations in the North and Norwegian Seas has been made. The previously unidentified alkylphenols in produced water have been characterised by means of alkylphenol retention indices (APRI) and mass spectrometry, and their total amounts estimated for the same nine locations. Our results confirm the presence of naphthols and other as yet unidentified compounds in produced water, while thiophenols were not detected by the used technique.     

Natural background and anthropogenic inputs of polycyclic aromatic hydrocarbons (PAH) in sediments of South-Western Barents Sea

Polycyclic aromatic hydrocarbons (PAH) were measured in sediment cores from 13 locations in South-Western Barents Sea as part of a detailed study of the Norwegian seabed under the MAREANO program. The generally low PAH levels found, an average around 200 ng g⁻¹ dry weight for sum PAH, indicate low inputs of petroleum hydrocarbons to the marine environment in the area. Differences in PAH composition and various PAH ratios indicate a natural, mostly petrogenic origin of PAH in sediments from the open sea locations, while the fjord locations show higher pyrogenic PAH contents with an increase towards upper sediment layers, indicating low inputs from human activities. Petrogenic PAH levels increase in deeper sediments at open sea locations, also when normalised to total organic carbon (TOC) contents, suggesting natural leakages of oil-related hydrocarbons in the area.