Signal-to-noise enhancement in ground-based intensity observations of solarp modes

Intensity observations of solarp modes are needed to form a complete picture of wave propagation in the photosphere. Ground-based intensity observations are severely hampered by terrestrial atmospheric noise. Partial cancellation of the noise power can be achieved if two spectra having disparate signal-to-noise ratios, and based on time series acquired simultaneously at the same site, are combined. A method of combining the spectra is suggested in which one amplitude is scaled and subtracted from the other. The result is squared yielding a positive-definite power density. To test the method, the intensity of light scattered by the Earths atmosphere was recorded at fifteen-second intervals in two narrow bands centered on 0.5 and 1.6. When the two resulting spectra were combined, the noise power was attenuated by a factor of 2.7. The scale factor was varied about its optimum value, revealing that noise peaks have a different signature than signal peaks, and opening up the possibility of a new tool in discrimination against noise peaks. Maxima at symmetry-allowed frequencies and minima at symmetry-forbidden frequencies indicate that the probability that these results are obtained by chance is only 6.1 × 10^–4. The positions of these maxima and minima also support the solar-cycle dependent frequency shifts found by Pallé, Régulo, and Roca Cortés (1990a).     

Identification of excess 40Ar by the 40Ar/39Ar age spectrum technique

⁴⁰Ar/³⁹Ar incremental heating experiments on igneous plagioclase, biotite, and pyroxene that contain known amounts of excess⁴⁰Ar indicate that saddle-shaped age spectra are diagnostic of excess⁴⁰Ar in igneous minerals as well as in igneous rocks. The minima in the age spectra approach but do not reach the crystallization age. Neither the age spectrum diagram nor the⁴⁰Ar/³⁶Ar versus³⁹Ar/³⁶Ar isochron diagram reliably reveal the crystallization age in such samples.     

Portales Valley: Petrology of a metallic‐melt meteorite breccia

Abstract— Portales Valley (PV) is an unusual metal‐veined meteorite that has been classified as an H6 chondrite. It has been regarded either as an annealed impact melt breccia, as a primitive achondrite, or as a meteorite with affinities to silicated iron meteorites. We studied the petrology of PV using a variety of geochemical‐mineralogical techniques. Our results suggest that PV is the first well‐documented metallic‐melt meteorite breccia. Mineral‐chemical and other data suggest that the protolith to PV was an H chondrite. The composition of FeNi metal in PV is somewhat fractionated compared to H chondrites and varies between coarse vein and silicate‐rich portions. It is best modeled as having formed by partial melting at temperatures of ?940–1150 °C, with incomplete separation of solid from liquid metal. Solid metal concentrated in the coarse vein areas and S‐bearing liquid metal concentrated in the silicate‐rich areas, possibly as a result of a surface energy effect. Both carbon and phosphorus must have been scavenged from large volumes and concentrated in metallic liquid. Graphite nodules formed by crystallization from this liquid, whereas phosphate formed by reaction between P‐bearing metal and clinopyroxene components, depleting clinopyroxene throughout much of the meteorite and growing coarse phosphate at metal‐silicate interfaces. Some phosphate probably crystallized from P‐bearing liquids, but most probably formed by solid‐state reaction at ?975‐725 °C. Phosphate‐forming and FeO‐reduction reactions were widespread in PV and entailed a change in the mineralogy of the stony portion on a large scale. Portales Valley experienced protracted annealing from supersolidus to subsolidus temperatures, probably by cooling at depth within its parent body, but the main differences between PV and H chondrites arose because maximum temperatures were higher in PV. A combination of a relatively weak shock event and elevated pre‐shock temperatures probably produced the vein‐and‐breccia texture, with endogenic heating being the main heat source for melting, and with stress waves from an impact event being an essential trigger for mobilizing metal. Portales Valley is best classified as an H7 metallic‐melt breccia of shock stage S1. The meteorite is transitional between more primitive (chondritic) and evolved (achondrite, iron) meteorite types and offers clues as to how differentiation could have occurred in some asteroidal bodies.     

A method to measure the isotopic (C) composition of dissolved organic carbon using a high temperature combustion instrument

The stable isotopes of dissolved organic carbon (DOC) are a powerful tool for distinguishing sources and inputs of organic matter in aquatic systems. While several methods exist to perform these analyses, no labs routinely utilize a high temperature combustion (HTC) instrument. Advantages of HTC instruments include rapid analysis, small sample volumes and minimal sample preparation, making them the favored devices for most routine oceanic DOC concentration measurements. We developed a stable carbon DOC method based around an HTC system. This method has the benefit of a simple setup, requiring neither vacuum nor high pressures. The main drawback of the method is a significant blank, requiring careful accounting of all blank sources for accurate isotopic and concentration values. We present here a series of experiments to determine the magnitude, source and isotopic composition of the HTC blank. Over time, the blank is very stable at  20 ng of carbon with a δ¹³C of − 18.1‰ vs. VPDB. The similarity of the isotopic composition of the blank and seawater samples makes corrections relatively minor. The precision of the method was determined by oxidizing organic standards with a wide isotopic and concentration range (− 9‰ to − 39‰; 18 μM to 124 μM). Analysis of seawater samples demonstrates the accuracy for low concentration, high salinity samples. The overall error on the measurement is approximately ± 0.8‰.     

Benefits of Software GPS Receivers for Enhanced Signal Processing

In this article, the architecture of a software Global Positioning System (GPS) receiver is described and an analysis is included of the performance of a software GPS receiver when tracking the GPS signals in challenging environments. Results are included that demonstrate the advantage of the software GPS receiver in tracking the GPS signals in low signal-to-noise or jamming scenarios. Various current and previous applications of the software GPS receiver are also described. ? 2000 John Wiley & Sons, Inc.     

Measurement of persistent organic pollutants (POPs) in plastic resin pellets from remote islands: toward establishment of background concentrations for International Pellet Watch

Plastic resin pellets collected from remote islands in the Pacific, Atlantic, and Indian Oceans and the Caribbean Sea were analyzed for polychlorinated biphenyls (PCBs), dichloro-diphenyltrichloroethane and its degradation products (DDTs), and hexachlorocyclohexanes (HCHs). Concentrations of PCBs (sum of 13 congeners) in the pellets were 0.1-9.9 ng/g-pellet. These were 1-3 orders of magnitude smaller than those observed in pellets from industrialized coastal shores. Concentrations of DDTs in the pellets were 0.8-4.1 ng/g-pellet. HCH concentrations were 0.6-1.7 ng/g-pellet, except for 19.3 ng/g-pellet on St. Helena, where current use of lindane is likely influence. This study provides background levels of POPs (PCBs<10 ng/g-pellet, DDTs <4 ng/g-pellet, HCHs <2 ng/g-pellet) for International Pellet Watch. Sporadic large concentrations of POPs were found in some pellet samples from remote islands and should be considered in future assessments of pollutants on plastic debris.     

A comparison of different magnetic methods for determining the relative grain size of magnetite in natural materials: Some results from lake sediments

A new rapid method for identifying relative grain size variations in magnetic involves the parameter anhysteretic susceptibility (χ_ARM, i.e. specific ARM obtained in a 1 Oe steady field), which is particularly sensitive to the single domain (SD) and small pseudo-single domain (PSD) grains of the finer magnetite fraction. A second parameter, low-field susceptibility (χ), is relatively more sensitive to the coarser magnetite fraction (larger PSD and smaller multidomain (MD) grains). We can then obtain a measure of the ratio of coarse- to fine-grain magnetite for large numbers of samples by plotting χ_ARversusχ. A simple idealized model based on sized magnetite samples is proposed to explain the use of the χ_ARMversusχ plot for detecting relative grain-size changes in the magnetic content of natural materials. The sediments of three lakes that contain magnetite or a similar magnetic carrier and have a wide range of values of χ_ARM and χ are used to test the model.The model is used to interpret the magnetic variations observed, and the interpretations are supported by high-field hysteresis measurements of the same sediments. The combination of the high-field hysteresis method of Day et al. [1] and the χ_ARM vs. χ method is a powerful technique allowing the rapid identification of both the relative grain size and domain state for large numbers of samples containing magnetite. The χ_ARMvs.χ method should be used as an intial means of identifying distinct groups of samples.The high-field hysteresis method should then be applied to a few representative samples from each group to confirm the initial interpretation.