Stable nonlinear methods for sensor array processing;     

Byrne  C. Steele  A. 《Oceanic Engineering, IEEE Journal of》1985,10(3):255-259

Most nonlinear high-resolution bearing estimators are unstable in the presence of correlated noise, system phase errors, and multipath arrivals because they inadvertently place too much emphasis on unstable eigenvectors of the cross-sensor correlation matrix. For moderately correlated noise there will be sufficiently many stable eigenvectors to resolve and localize discrete sources. A method is given (the "stable nonlinear method" or SNLM) whereby reweighting of the eigenvectors is achieved implicitly, without actual calculation of the eigenvectors. This SNLM is compared with Capon's maximum likelihood method (MLM) in simulations of correlated noise, partially correlated signals, and phase errors, and is shown to provide good stability in the cases considered.  相似文献   

Solubility of hydrous ferric oxide and iron speciation in seawater     

Robert H. Byrne  Dana R. Kester 《Marine Chemistry》1976,4(3):255-274

Iron solubility equilibria were investigated in seawater at 36.22‰ salinity and 25°C using several filtration and dialysis techniques. In simple filtration experiments with 0.05 μm filters and Millipore ultra-filters, ferric chlorides fluorides, sulfates, and FeOH²⁺ species were found to be insignificant relative to Fe(OH)₂⁺ at p[H⁺] = ?log [H⁺] greater than 6.0. Hydrous ferric oxide freshly precipitated from seawater yielded a solubility product of ${}^1\text{K}{}_{\mathrm{<mtext>so</mtext>}}\text{=}\text{[Fe}{}^{\mathrm{3+}}\text{][H}{}^{\mathrm{+}}\text{]}{}^{\mathrm{?3}}\text{= 4.7 · 10}{}^5$. Solubility studies based on the rates of dialysis of various seawater solutions and on the filtration of acidified seawater solutions indicated the existence of the Fe(OH)₃⁰ species. The formation constant for this species can be calculated as ${}^1\text{β}{}_3\text{=}\text{[Fe(OH)}{}_3{}^0\text{] [H}{}^{\mathrm{+}}\text{]}{}^3\text{/[Fe}{}^{\mathrm{3+}}\text{] = 2.4 · 10}{}^{\mathrm{?14}}$. The Fe(OH)₄^? species is present at concentrations which are negligible compared to Fe(OH)₂⁺ and Fe(OH)₃⁰ in the normal pH range of seawater. However, there is at least one other significant ferric complex in seawater above p[H⁺] = 8.0 (possibly with bicarbonate, carbonate, or borate ions) in addition to the Fe(OH)₂⁺ and Fe(OH)₃⁰ species.  相似文献   

A permanent seismic station beneath the Ocean Bottom     

David Harris  Robert K. Cessaro  Fred K. Duennebier  David A. Byrne 《Marine Geophysical Researches》1987,9(1):67-94

The Hawaii Institute of Geophysics began development of the Ocean Subbottom Seisometer (OSS) system in 1978, and OSS systems were installed in four locations between 1979 and 1982. The OSS system is a permanent, deep ocean borehole seismic recording system composed of a borehole sensor package (tool), an electromechanical cable, recorder package, and recovery system. Installed near the bottom of a borehole (drilled by the D/V Glomar Challenger), the tool contains three orthogonal, 4.5-Hz geophones, two orthogonal tilt meters; and a temperature sensor. Signals from these sensors are multiplexed, digitized (with a floating point technique), and telemetered through approximately 10 km of electromechanical cable to a recorder package located near the ocean bottom. Electrical power for the tool is supplied from the recorder package. The digital seismic signals are demultiplexed, converted back to analog form, processed through an automatic gain control (AGC) circuit, and recorded along with a time code on magnetic tape cassettes in the recorder package. Data may be recorded continuously for up to two months in the self-contained recorder package. Data may also be recorded in real time (digital formal) during the installation and subsequent recorder package servicing. The recorder package is connected to a submerged recovery buoy by a length of bouyant polypropylene rope. The anchor on the recovery buoy is released by activating either of the acoustical command releases. The polypropylene rope may also be seized with a grappling hook to effect recovery. The recorder package may be repeatedly serviced as long as the tool remains functionalA wide range of data has been recovered from the OSS system. Recovered analog records include signals from natural seismic sources such as earthquakes (teleseismic and local), man-made seismic sources such as refraction seismic shooting (explosives and air cannons), and nuclear tests. Lengthy continuous recording has permitted analysis of wideband noise levels, and the slowly varying parameters, temperature and tilt.Hawaii Institute of Geophysics Contribution 1909.  相似文献   

A simple shaker table for seismometer calibration   总被引：1，自引：0，他引：1  

Frederick K. Duennebier  George H. Sutton  David Harris  David A. Byrne 《Marine Geophysical Researches》1984,6(3):311-328

A unique and simple shaker table (shake table or shaking table), designed, constructed, and installed at the Hawaii Institute of Geophysics, has proven to be a valuable aid in testing and calibrating short period seismometers, as well as ocean bottom and ocean sub-bottom seismometer/tilt meter packages. It consists of a platform suspended in a stairwell by a single elastic cord (10 m extended length) driven by GeoSpace HS-10 geophones. Platform motion is monitored by orthogonal reference geophones and tilt meters. The relatively low natural periods of the platform, about 1.9 sec vertical and 6.5 sec horizontal, provide sufficient isolation from local vibrations that calibration can be made near operational amplitudes. Vertical or horizontal driver geophones can be driven by a commercial signal generator or white noise generator, or from magnetic tape output. The table can also be tilted with respect to the drivers to determine tilt tolerances and to calibrate tilt meters. A Hewlett-Packard 3582-A spectrum analyzer, used to analyze both reference and output signals, provides near real-time system cabibration and is an efficient means for investigating parasitic system resonances. The analyzer can also provide a white noise signal source to the driver geophones.Hawaii Institute of Geophysics Contribution 1443.  相似文献   

Inorganic speciation of dissolved elements in seawater: the influence of pH on concentration ratios     

Robert H Byrne 《Geochemical transactions》2002,3(1):11-6

Assessments of inorganic elemental speciation in seawater span the past four decades. Experimentation, compilation and critical review of equilibrium data over the past forty years have, in particular, considerably improved our understanding of cation hydrolysis and the complexation of cations by carbonate ions in solution. Through experimental investigations and critical evaluation it is now known that more than forty elements have seawater speciation schemes that are strongly influenced by pH. In the present work, the speciation of the elements in seawater is summarized in a manner that highlights the significance of pH variations. For elements that have pH-dependent species concentration ratios, this work summarizes equilibrium data (S = 35, t = 25°C) that can be used to assess regions of dominance and relative species concentrations. Concentration ratios of complex species are expressed in the form log[A]/[B] = pH - C where brackets denote species concentrations in solution, A and B are species important at higher (A) and lower (B) solution pH, and C is a constant dependent on salinity, temperature and pressure. In the case of equilibria involving complex oxy-anions (MO _x (OH) _y ) or hydroxy complexes (M(OH) _n ), C is written as pK _n = -log K _n or pK _n * = -log K _n * respectively, where K _n and K _n * are equilibrium constants. For equilibria involving carbonate complexation, the constant C is written as pQ = -log(K ₂ ^l K _n [HCO₃ ^-]) where K ₂ ^l is the HCO₃ ^- dissociation constant, K _n is a cation complexation constant and [HCO₃ ^-] is approximated as 1.9 × 10^-3 molar. Equilibrium data expressed in this manner clearly show dominant species transitions, ranges of dominance, and relative concentrations at any pH.  相似文献   

Determination of _SO4β₁ for yttrium and the rare earth elements at I = 0.66 m and t = 25°C—implications for YREE solution speciation in sulfate-rich waters     

Johan Schijf  Robert H. Byrne 《Geochimica et cosmochimica acta》2004,68(13):2825-2837

We present a complete set of stability constants (_SO4β₁) for the monosulfato-complexes of yttrium and the rare earth elements (YREE), except Pm, at I = 0.66 m and t = 25°C, where _SO4β₁ = [MSO₄⁺] × [M³⁺]⁻¹[SO₄²⁻]⁻¹ (M ≡ YREE and brackets indicate free ion concentrations on the molal scale). Stability constants were determined by investigating the solubility of BaSO₄ in concentrated aqueous solutions of MCl₃. This is the first complete set to be published in more than 30 years.The resulting _SO4β₁ pattern is very similar in shape to one reported by de Carvalho and Choppin (1967a) (I = 2 mol/L; t = 25°C) that has been largely ignored. Stability constants vary little between La and Sm, but display a weak maximum at Eu. Between Eu and Lu, _SO4β₁ decreases by 0.2 log units, substantially exceeding the ±0.02 log unit average analytical precision. The stability constant for Y is approximately equal to that for Er. Our _SO4β₁ pattern is consequently distinctly different from the consensus pattern, based on a single data set from 1954, which is essentially flat, with a range of only 0.07 log units between the lowest and highest _SO4β₁ values within the lanthanide series (excluding Y).Values of _SO4β₁ obtained in this work, in conjunction with the ion-pairing model of Millero and Schreiber (1982), allow prediction of _SO4β₁ between 0 and 1 m ionic strength. These results are used to assess both the absolute and relative extent of YREE sulfate complexation in acidic, sulfate-rich waters.  相似文献   

A catalogue of major and trace element data for Icelandic Holocene silicic tephra layers     

RH. H. Meara  TH. Thordarson  N. J. G. Pearce  C. Hayward  G. Larsen 《第四纪科学杂志》2020,35(1-2):122-142

Tephra layers with Icelandic provenance have been identified across the North Atlantic region in terrestrial, lacustrine, marine and glacial environments. These tephra layers are used as marker horizons in tephrochronology including climate studies, archaeology and environmental change. The major element chemistries of 19 proximally deposited Holocene Icelandic silicic tephra layers confirm that individual volcanic systems have unique geochemical signatures and that eruptions from the same system can often be distinguished. In addition, glass trace element chemistry highlights subtle geochemical variations between tephra layers which appear to have identical major element chemistry and thus allows for the identification of some, if not all, tephra layers previously considered identical in composition. This paper catalogues the compositional variation between the widespread Holocene Icelandic silicic tephra deposits.  相似文献   

Copper(II) carbonate complexation in seawater     

Robert H. Byrne  William L. Miller 《Geochimica et cosmochimica acta》1985,49(8):1837-1844

Cupric carbonate and cupric bicarbonate complexation constants were determined in natural seawater and in a variety of synthetic media. The formation constants of CuHCO₃⁺, CuCO₃⁰ and Cu(CO₃)₂^2? at 25°C and zero ionic strength are: log β_H⁰ = 1.8, log β₁⁰ = 6.82 and log β⁰₂ = 10.6. Formation constants of these species appropriate to 0.7 molar ionic strength and 25°C are log β_H ～- 1, log β₁ = 5.73, log β₂ = 9.3. Our results indicate that the inorganic speciation scheme of Cu(II) in seawater is dominated by CuCO₃⁰ and that the ternary species, CuCO₃OH^?, is of substantial importance.  相似文献   

Use of Pitzer's equations to determine the media effect on the formation of lead chloro complexes     

Frank.J. Millero  Robert H. Byrne 《Geochimica et cosmochimica acta》1984,48(5):1145-1150

The spectrophotometric measurements of chloro complexes of lead in aqueous HCl, NaCl, MgCl₂ and CaCl₂ solutions at 25°C have been analyzed using Pitzer's specific interaction equations. Parameters for activity coefficients of the complexes PbCl⁺, PbCl₂⁰ and PbCl₃^? have been determined for the various media. Values of $\text{K}{}_1\text{= 30.0 ± 0.6}$, $\text{K}{}_2\text{= 106.7 ± 2.1}$ and $\text{K}{}_3\text{= 73.0 ± 1.5}$ were obtained for the cumulative formation constants. [$\text{Pb}{}^{\mathrm{2+}}\text{+ nCl}{}^{\mathrm{?}}\text{→ PbCl}{}_{\mathrm{n}}{}^{\mathrm{2?n}}\text{)}$]. These values are in reasonable agreement with literature data. The Pitzer parameters for the PbCl ion pairs in various media were used to calculate the speciation of Pb²⁺ in an artificial seawater solution.  相似文献   

辽宁盖县梁屯—矿洞沟碱性正长岩杂岩体的U—Pb和Sm—Nd年龄及其地质意义   总被引：17，自引：14，他引：17  

蔡剑辉  阎国翰  牟保磊  许保良  邵宏翔  许荣华 《岩石学报》2002,18(3):349-354

辽宁梁屯 -矿洞沟杂岩体主要由辉石正长岩、霓辉正长岩和霓辉角闪正长岩等碱性岩石组成 ,具有全岩 Rb- Sr等时线年龄 186 6± 115 Ma和 ISr=0 .70 4 9的同位素特征 ,是我国目前报道的最古老的碱性正长岩类。本文报道了该岩体的锆石U- Pb和全岩 Sm- Nd同位素测试资料 ,获得了锆石 U- Pb同位素年龄为 185 7± 2 0 Ma、Sm- Nd等时年龄为 1787± 180 Ma、εNd(t) =- 4 .8～ - 5 .0的数据。它们反映出该杂岩体形成年龄的上限为 185 7± 2 0 Ma、下限不小于 1787± 180 Ma,来源于富集地幔物质。基于这些数据并结合区域地质资料分析 ,作者提出了华北地台北缘古元古宙存在有富集地幔储库 ,以及辽河群主体形成于 190 0 Ma以前的认识  相似文献