Dip‐adaptive singular‐value decomposition filtering for seismic reflection enhancement     

Milton J. Porsani  Bjorn Ursin  Michelângelo G. Silva  Paulo E. M. Melo 《Geophysical Prospecting》2013,61(1):42-52

We present a singular value decomposition (SVD) filtering method for the enhancement of coherent reflections and for attenuation of noise. The method is applied in two steps. First normal move‐out (NMO) correction is applied to shot or CMP records, with the purpose of flattening the reflections. We use a spatial SVD filter with a short sliding window to enhance coherent horizontal events. Then the data are sorted in common‐offset panels and the local dip is estimated for each panel. The next SVD filtering is performed on a small number of traces and a small number of time samples centred around the output sample position. Data in a local window are corrected for linear moveout corresponding to the dips before SVD. At the central time sample position, we sum over the dominant eigenimages of a few traces, corresponding to SVD dip filtering. We illustrate the method using land seismic data from the Tacutu basin, located in the north‐east of Brazil. The results show that the proposed method is effective and is able to reveal reflections masked by ground‐roll and other types of noise.  相似文献   

Assessment of the European Standard for the determination of resistance of marble to thermal and moisture cycles: recommendations for improvements     

Rossana Bellopede  Eleonora Castelletto  Bjorn Schouenborg  Paola Marini 《Environmental Earth Sciences》2016,75(11):946

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Protein content and amino acid composition of young Atlantic halibut (Hippoglossus hippoglossus L.) captured in the autumn in north Norway     

Andreasen  Thomas Venno; Gulliksen  Bjorn; Haug  Tore; Nilsen  Einar M.; Ringo  Einar 《ICES Journal of Marine Science》1993,50(1):93-100

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Partitioning of Ni between olivine and silicate melt: the “Henry's law problem” reexamined: discussion     

Bjorn Mysen 《Geochimica et cosmochimica acta》1982,46(2):297-298

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Introduction: a tribute to Hatten S. Yoder, Jr. on his 80th birthday     

Bjorn Mysen 《Geochimica et cosmochimica acta》2002,66(12):2071-2072

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Optimal temperature for growth and feed conversion of immature cod (Gadus morhua L.)   总被引：1，自引：0，他引：1  

Bjornsson  Bjorn; Steinarsson  Agnar; Oddgeirsson  Matthias 《ICES Journal of Marine Science》2001,58(1):29-38

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Effects of anthropogenic feeding on the growth rate, nutritional status and migratory behaviour of free-ranging cod in an Icelandic fjord     

Bjornsson  Bjorn 《ICES Journal of Marine Science》2002,59(6):1248-1255

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Solubility mechanisms of fluorine in peralkaline and meta-aluminous silicate glasses and in melts to magmatic temperatures     

Bjorn O. Mysen  George D. Cody 《Geochimica et cosmochimica acta》2004,68(12):2745-2769

Structural interaction between dissolved fluorine and silicate glass (25°C) and melt (to 1400°C) has been examined with ¹⁹F and ²⁹Si MAS NMR and with Raman spectroscopy in the system Na₂O-Al₂O₃-SiO₂ as a function of Al₂O₃ content. Approximately 3 mol.% F calculated as NaF dissolved in these glasses and melts. From ¹⁹F NMR spectroscopy, four different fluoride complexes were identified. These are (1) Na-F complexes (NF), (2) Na-Al-F complexes with Al in 4-fold coordination (NAF), (3) Na-Al-F complexes with Al in 6-fold coordination with F (CF), and (4) Al-F complexes with Al in 6-fold, and possibly also 4-fold coordination (TF). The latter three types of complexes may be linked to the aluminosilicate network via Al-O-Si bridges.The abundance of sodium fluoride complexes (NF) decreases with increasing Al/(Al + Si) of the glasses and melts. The NF complexes were not detected in meta-aluminosilicate glasses and melts. The NAF, CF, and TF complexes coexist in peralkaline and meta-aluminosilicate glasses and melts.From ²⁹Si-NMR spectra of glasses and Raman spectra of glasses and melts, the silicate structure of Al-free and Al-poor compositions becomes polymerized by dissolution of F because NF complexes scavenge network-modifying Na from the silicate. Solution of F in Al-rich peralkaline and meta-aluminous glasses and melts results in Al-F bonding and aluminosilicate depolymerization.Temperature (above that of the glass transition) affects the Qⁿ-speciation reaction in the melts, 2Q³ ⇔ Q⁴ + Q², in a manner similar to other alkali silicate and alkali aluminosilicate melts. Dissolved F at the concentration level used in this study does not affect the temperature-dependence of this speciation reaction.  相似文献   

Solubility and solution mechanism of H₂O in alkali silicate melts and glasses at high pressure and temperature   总被引：2，自引：0，他引：2  

Bjorn O. Mysen  George D. Cody 《Geochimica et cosmochimica acta》2004,68(24):5113-5126

The solubility behavior of H₂O in melts in the system Na₂O-SiO₂-H₂O was determined by locating the univariant phase boundary, melt = melt + vapor in the 0.8-2 GPa and 1000°-1300°C pressure and temperature range, respectively. The NBO/Si-range of the melts (0.25-1) was chosen to cover that of most natural magmatic liquids. The H₂O solubility in melts in the system Na₂O-SiO₂-H₂O (X_H2O) ranges between 18 and 45 mol% (O = 1) with (∂X_H2O/∂P)_T∼14-18 mol% H₂O/GPa. The (∂X_H2O/∂P)_T is negatively correlated with NBO/Si (= Na/Si) of the melt. The (∂X_H2O/∂T)_P is in the −0.03 to +0.05 mol% H₂O/°C range, and is negatively correlated with NBO/Si. The [∂X_H2O/∂(NBO/Si)]_P,T is in the −3 to −8 mol% H₂O/(NBO/Si) range. Melts with NBO/Si similar to basaltic liquids (∼0.6-∼1.0) show (∂X_H2O/∂T)_P<0, whereas more polymerized melts exhibit (∂X_H2O/∂T)_P>0. Complete miscibility between hydrous melt and aqueous fluid occurs in the 0.8-2 GPa pressure range for melts with NBO/Si ≤0.5 at T >1100°C. Miscibility occurs at lower pressure the more polymerized the melt.  相似文献   

Fractionation of major elements between coexisting H₂O-saturated silicate melt and silicate-saturated aqueous fluids in aluminosilicate systems at 1-2 GPa     

Bjorn O Mysen  Jessica Shang 《Geochimica et cosmochimica acta》2003,67(20):3925-3936

From experimental data in the systems Na₂O-Al₂O₃-SiO₂-H₂O, K₂O-Al₂O₃-SiO₂-H₂O at 1100°C, and CaO-Al₂O₃-SiO₂-H₂O at 1200°C in the 1-2 GPa pressure range, the solution behavior of the individual oxides in coexisting H₂O-saturated silicate melts and silicate-saturated aqueous fluids appears to be incongruent. Recalculated on an anhydrous basis, in the CaO-Al₂O₃-SiO₂-H₂O system, CaO^fluid/CaO^melt < 1, whereas in the Na₂O-Al₂O₃-SiO₂-H₂O and K₂O-Al₂O₃-SiO₂-H₂O systems, K₂O^fluid/K₂O^melt and Na₂O^fluid/Na₂O^melt both are greater than 1. The aqueous fluids are depleted in alumina relative to silicate melt.In the Na₂O-Al₂O₃-SiO₂-H₂O, K₂O-Al₂O₃-SiO₂-H₂O, and CaO-Al₂O₃-SiO₂-H₂O systems, fluid/melt partition coefficients for the individual oxides range between ∼0.005 and 0.35 depending on oxide, bulk composition and pressure. The alkali partition coefficients are about an order of magnitude higher than that of CaO. Alumina and silica partition coefficient values in the CaO-Al₂O₃-SiO₂-H₂O system are 10-20% of the values for the same oxides in the Na₂O-Al₂O₃-SiO₂-H₂O and K₂O-Al₂O₃-SiO₂-H₂O systems.Positive correlations among individual partition coefficients and oxide concentrations in the aqueous fluids are consistent with complexing in the fluid that involves silicate polymers associated with alkalis and alkaline earths and aluminosilicate complexes where alkalis and alkaline earths may serve to charge-balance Al³⁺, which is, perhaps, in tetrahedral coordination. Alkali aluminosilicate complexes in aqueous fluid appear more stable than Ca-aluminosilicate complexes.  相似文献