Regional geopotential model improvement for the Iranian geoid determination   总被引：1，自引：0，他引：1  

Georg Weber  Hossein Zomorrodian 《Journal of Geodesy》1988,62(2):125-141

Spherical harmonic expansions of the geopotential are frequently used for modelling the earth’s gravity field. Degree and order of recently available models go up to 360, corresponding to a resolution of about50 km. Thus, the high degree potential coefficients can be verified nowadays even by locally distributed sets of terrestrial gravity anomalies. These verifications are important when combining the short wavelength model impact, e.g. for regional geoid determinations by means of collocation solutions. A method based on integral formulae is presented, enabling the improvement of geopotential models with respect to non-global distributed gravity anomalies. To illustrate the foregoing, geoid computations are carried out for the area of Iran, introducing theGPM2 geopotential model in combination with available regional gravity data. The accuracy of the geoid determination is estimated from a comparison with Doppler and levelling data to ±1.4m.  相似文献   

Nitrogen and sulfur species in Antarctic aerosols at Mawson,Palmer Station,and Marsh (King George Island)   总被引：4，自引：0，他引：4  

D. L. Savoie  J. M. Prospero  R. J. Larsen  F. Huang  M. A. Izaguirre  T. Huang  T. H. Snowdon  L. Custals  C. G. Sanderson 《Journal of Atmospheric Chemistry》1993,17(2):95-122

High volume bulk aerosol samples were collected continuously at three Antarctic sites: Mawson (67.60° S, 62.50° E) from 20 February 1987 to 6 January 1992; Palmer Station (64.77° S, 64.06° W) from 3 April 1990 to 15 June 1991; and Marsh (62.18° S, 58.30° W) from 28 March 1990, to 1 May 1991. All samples were analyzed for Na⁺, SO ₄ ^2– , NO ₃ ^– , methanesulfonate (MSA), NH ₄ ⁺ ,²¹⁰Pb, and⁷Be. At Mawson for which we have a multiple year data set, the annual mean concentration of each species sometimes vary significantly from one year to the next: Na⁺, 68–151 ng m^–3; NO ₃ ^– , 25–30 ng m^–3; nss SO ₄ ^2– , 81–97 ng m^–3; MSA, 19–28 ng m^–3; NH ₄ ⁺ , 16–21 ng m^–3;²¹⁰Pb, 0.75–0.86 fCi m^–3. Results from multiple variable regression of non-sea-salt (nss) SO ₄ ^2– with MSA and NO ₃ ^– as the independent variables indicates that, at Mawson, the nss SO ₄ ^2– /MSA ratio resulting from the oxidation of dimethylsulfide (DMS) is 2.80±0.13, about 13% lower than our earlier estimate (3.22) that was based on 2.5 years of data. A similar analysis indicates that the ratio at Palmer is about 40% lower, 1.71±0.10, and more comparable to previous results over the southern oceans. These results when combined with previously published data suggest that the differences in the ratio may reflect a more rapid loss of MSA relative to nss SO ₄ ^2– during transport over Antarctica from the oceanic source region. The mean²¹⁰Pb concentrations at Palmer and Marsh and the mean NO ₃ ^– concentration at Palmer are about a factor of two lower than those at Mawson. The²¹⁰Pb distributions are consistent with a²¹⁰Pb minimum in the marine boundary layer in the region of 40°–60° S. These features and the similar seasonalities of NO ₃ ^– and²¹⁰Pb at Mawson support the conclusion that the primary source regions for NO ₃ ^– are continental. In contrast, the mean concentrations of MSA, nss SO ₄ ^2– , and NH ₄ ⁺ at Palmer are all higher than those at Mawson: MSA by a factor of 2; nss SO ₄ ^2– by 10%; and NH ₄ ⁺ by more than 50%. However, the factor differences exhibit substantial seasonal variability; the largest differences generally occur during the austral summer when the concentrations of most of the species are highest. NH ₄ ⁺ /(nss SO ₄ ^2– +MSA) equivalent ratios indicate that NH₃ neutralizes about 60% of the sulfur acids during December at both Mawson and Palmer, but only about 30% at Mawson during February and March.  相似文献   

Tungsten skarn mineralizations in a regional metamorphic terrain in northern Norway: a possible metamorphic ore deposit   总被引：2，自引：0，他引：2  

R. Berg Larsen 《Mineralium Deposita》1991,26(4):281-289

Scheelite- and molybdenite-bearing scapolite skarn and plagioclase skarn occur as stratabound mineralizations in a terrain which has suffered regional metamorphism. Scapolite skarn formed as replacement skarns in plagioclase-bearing hornblendic gneiss whereas plagioclase skarn precipitated in fractures as vein skarn mineralizations. The genesis of these skarn deposits are closely connected to an episode of boudinage on the limbs of a large-scale dome-shaped fold. Fluid inclusion studies revealed that the ore-forming fluids were composed of CO₂ with 2 to 17 mole% CH₄, which formed due to decarbonation reactions during peak metamorphism at the end of the Caledonian orogenesis. Thermodynamic considerations indicate that scapolite and plagioclase formed above 550 °C and 2 Kbar pressure and were followed by precipitation of scheelite between 400 and 570 °C.  相似文献   

Separation of aquatic humic material before and after chlorination using high-performance size exclusion chromatography     

Georg Becher  Georg E. Carlberg 《Organic Geochemistry》1985,8(1):107

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Sr-gorceixite,a weathering product in rich iron ores from the Córrego do Feijão Mine,Minas Gerais,Brazil     

Wania Greiffo  Klaus Herrmann  Georg Müller  Karl W. Strauss 《Contributions to Mineralogy and Petrology》1984,87(4):418-419

A sulfate-bearing Sr-Ba phosphate (Sr-gorceixite) formed by supergene alteration in rich iron ores from Minas Gerais, Brazil, has been studied by means of microprobe techniques. Analytical data and the structural formula are presented.  相似文献   

Mixed valence of iron in minerals with cation clusters     

Georg Amthauer  George R. Rossman 《Physics and Chemistry of Minerals》1984,11(1):37-51

The valence and distribution of iron in vivianite, lazulite, babingtonite, rockbridgeite, acmite, aegirine-augite, hedenbergite, and ilvaite were studied with optical and Mössbauer spectroscopy. Optically activated intervalence charge transfer between Fe²⁺ and Fe³⁺ in neighboring sites through common edges or faces is observed in all these minerals irrespective of the polymerization of the iron-oxygen polyhedra ranging from finite clusters to infinite structural units. However, a distinct decrease occurs in the energy of the corresponding optical absorption band with increasing number of Fe²⁺ and Fe³⁺ ions involved in the charge transfer process. Thermally activated electron delocalization between Fe²⁺ and Fe³⁺ occurs only if Fe²⁺ and Fe³⁺ occupy crystallographically equivalent or geometrically very similar neighboring sites which share common edges to form extended structural units such as the ribbon in ilvaite. If the Fe-O polyhedra form finite clusters of two, three, or four polyhedra (e.g., in vivianite, lazulite, and babingtonite, respectively) no thermally-activated mixed-valence states of iron are observed. In aegirine, extended regions of the M1 chain are statistically occupied by Fe²⁺ and Fe³⁺ giving rise to thermally-activated electron delocalization in addition to the intervalence band in the optical absorption spectrum. The intensity of the optical intervalence absorption has been measured in a number of systems: ? values range from 60 to 210.  相似文献   

Slab weakening: Mechanical and thermal-mechanical consequences for slab detachment     

Shoichi  Yoshioka David A.  Yuen Tine B.  Larsen 《Island Arc》1995,4(2):89-103

Abstract Slab detachment is a geophysical instability whose manifestation can be revealed by seismic tomography. Evidence of this phenomenon is in the Dinarides/Hellenic and the New Hebrides subduction zones. Subducted slabs in these regions are torn horizontally at depths ranging from 100 to 300 km. We constructed a viscoelastic three-dimensional finite element model and investigated the state of stress. We found that an area with high stress concentration of the order of several hundred MPa is formed near the tip of the tear inside the slab, which can cause lateral migration of the tear. Favorable conditions for slab detachment are characterized by large interplate frictional force at a subduction zone and small slab resistance force deeper down. Stress concentration increases with the down-dip tension inside the slab. The phenomenon of slab weakening has also been studied from a thermal-mechanical standpoint, using a two-dimensional convection model with non-Newtonian, temperature-dependent rheology. The stress-dependent rheology plays an important role in causing local weakening of the descending slab. In strongly time-dependent situations the fast descending slab is not strong everywhere but has a weak region in the middle, making it vulnerable to slab detachment. The presence of viscous heating will enhance slab detachment tendency by further weakening the interior by the frictional heating. Besides these effects, there are other mechanisms which can also weaken the slab interior and help to make slabs more pliable and susceptible to detachment.  相似文献   

Titanian chondrodite and clinohumite in marbles from the Ötztal crystalline basement     

Karin Ehlers  Dr. Georg Hoinkes 《Mineralogy and Petrology》1987,36(1):13-25

Summary Marble lenses within the polymetamorphic Ötztal crystalline complex frequently contain pockets of clinohumite and chondrodite and their titanium-rich varieties. Chondrodites contain up to 9.1 wt% TiO₂ and clinohumites about half that amount. The maximum amounts of Ti in both minerals do not exeed values of 0.4 in the formula. XTi and X_F are correlated by a slope of –1, indicating the efficiency of the TiO₂Mg_–1F_–2 substitution at constant OH (Evans andTrommsdorff, 1983). Clinohumites sometimes contain lamellae which have nonstoichiometric cation ratios reflecting a composition between clinohumite and olivine. In many cases Ti-rich clinohumites and chondrodites coexist with Mg-ilmenite. Ti-rich clinohumites and chondrodites often break down to a symplectite of Ti-poor clinohumite (or olivine) and Mg-ilmenite. Parts of the marbles, which are barren of Mg-ilmenite contain F-rich clinohumites. The latter do not show any signs of breakdown features. We conclude therefore that fluorine stabilizes the humite group minerals to a wide range of metamorphic conditions. Ti-rich humite-group minerals are not stable till amphibolite facies conditions, and below F-rich humite-group minerals and olivine are the more stable phases in a H₂O-rich, SiO₂-poor carbonate system.

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Titanreiche Chondrodite und Klinohumite in Marmoren des Ötztalkristallins.

Zusammenfassung In Marmorlinsen des polymetamorphen Ötztalkristaliins kommen häufig titanarme und titanreiche Clinohumite und Chondrodite vor. Die höchsten Titan-Gehalte in Chondrodit betragen 9.1 Gew.-% TiO₂ während Clinohumite nur etwa die Hälfte dieses Wertes enthalten. Dies entspricht einem Maximalgehalt an Titan von 0.4 in den Formeln von Chondrodit und Clinohumit. Eine negative Korrelation zwischen X_Ti, und X_F mit der Steigung von –1 bestätigt die Wirksamkeit der Substitution TiO₂Mg_–1F_–2 bei konstantem OH (Evans undTrommsdorff, 1983). In Clinohumiten konnten nichtstöchiometrische Lamellen nachgewiesen werden, die chemisch zwischen Clinohumit und Olivin zusammengesetzt sind. Ti-reiche Clinohumite und Chondrodite koexistieren immer mit Mg-Ilmenit und wandeln sich häufig an ihren Rändern in einen Symplektit von Ti-ärmerem Clinohumit oder Olivin und Mg-Ilmenit um. In den Mg-Ilmenit freien Bereichen der Marmore kommen stets Ti-arme aber F-reiche Clinohumite vor, die niemals randliche Umwandlungserscheinungen zeigen. Die grobkörnigen (mm-großen) Humitminerale werden der variszischen Metamorphose in Amphibolitfazies zugeschrieben, während die Symplektite als Produkte der eoalpinen grünschieferfaziellen Überprägung angesehen werden. Wir schließen daraus, daß die Humitminerale durch Fluor in einem großen Bereich metamorpher Bedingungen stabilisiert werden, während Ti-reiche Humitminerale bei Bedingungen der Grünschieferfazies instabil werden und F-reiche Humitminerale und Olivin die stabilen Phasen in einem H₂O-reichen, SiO₂-armen Karbonatsystem sind.

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Polymetamorphose und Deckenbau der Strand-Halbinsel/SW-Norwegen     

Prof. Dr. Georg Müller  Dr. Karl W. Strauss 《International Journal of Earth Sciences》1987,76(2):407-418

Zusammenfassung Die Metamorphite der Halbinsel Strand / SW-Norwegen gehören zu einem Deckensystem präkambrischer Gesteine, das während der kaledonischen Orogenese von NNW her auf den Baltischen Schild geschoben worden ist (Sigmond Kildal 1978). Eine hangende Deckeneinheit umfa\t Metagranite, Melagabbroide und Gneise. Ihr granulitfazieller Mineralbestand (Metamorphosealter 1,5 Milliarden Jahre) wurde wahrscheinlich vor 1,18 Milliarden Jahren grünschieferfaziell retrograd überprägt. Die Decke ist nur noch in kleinen Erosionsinseln vorhanden. Eine liegende Dekkeneinheit besteht aus metasedimentären Gesteinen. Sie weist Mineralbestände der höheren Amphibolitfazies auf, die ebenfalls grünschieferfaziell überprägt wurden. Die Al^VI-Gehalte der bei beiden metamorphen Prozessen gebildeten Amphibole deuten bei Anwendung eines Diagramms vonRaase (1974) an, da\ die retrograde Metamorphose hier bei höheren Drücken ablief als die ältere Metamorphose. Ein Gesamtgesteinsalter von 1,16 Milliarden Jahren scheint für diese grünschieferfazielle Metamorphose das gleiche orogene Ereignis anzuzeigen wie für die hangende Einheit. Produkt der schwachen kaledonischen Metamorphose (400 Millionen Jahre) ist Stilpnomelan, der auch im Grundgebirge des Baltischen Schildes auftritt.

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The Strand Peninsula, Stavanger district, Southwestern Norway, has become well known, when V. M.Goldschmidt (1920) published his hypothesis of regional metasomatism. All rocks of the Strand area were assumed to be situated in autochthonous position. The main point ofGoldschmidt's hypothesis was progarde metamorphism of argillaceous sediments and their transformation to albite schists and plagioclase gneisses by metasomatic solutions given off from intruded trondhjemitic magmas.However, in contrast toGoldschmidt's ideas, the granitoid sill of the Ormakam-Moldhesten area, Strand Peninsula, and its wall rocks, which played an important role inGoldschmidt's discussion, are now found to be parts of a polymetamorphous thrust unit.Granulite facies assemblages, mainly consisting of orthopyroxene +clinopyroxene+plagioclase+hastingsite±orthoclase and quartz, have been partially replaced by lowgrade assemblages. Probably, the high-grade metamorphism has an age of about 1.5 Ga (Andresen &Heier 1975) whereas the age of the greenschist facies event may be conform to an orogenic cycle at about 1.15 Ga (Sigmond Kildal 1978).A lower nappe, covering the Strand Peninsula for its most parts, was subject of a petrologic re-examination using the microscope and the microprobe analyser. Its contacts with the hanging nappe as well as those with the underlying gneissic basement are characterized by thrust planes and horizons of phyllonites and cataclasites inside of the nappe and by local brecciation in the uppermost zones of the basement.The rocks of the lower nappe have been formed a long with the upper amphibolite facies as indicated by the following mineral assemblage: andesine + hastingsite and Mg-hornblende + quartz +biotite.Obviously, an inverse order of temperature regimes is recognizable in the allochthonous units. Maximum temperature of the upper nappe reached 800C (Müller &Herbert 1984) whereas T_max of the lower nappe did not exceed 750C.Using a diagram ofRaase (1974) the Al^VI-contents of the primary hastingsitic hornblendes of the lower nappe rocks indicate pressures which range distinctly below 5 kbars, whereas the secondary pargasitic hornblendes were formed at pressures of about 5 kbars. Probably the thrusting happened before the formation of secondary hornblendes took place. The load pressure in the lower nappe (< 5 kbars) was distinctly increased when the upper nappe was thrusted upon the lower one. Consequently the Al^VI-contents of secondary hornblendes indicate increased pressure ( 5 kbars).In the gneisses of the lower nappe late fractures were filled by stilpnomelane, chlorite and quartz. Very probably this depends on thrust movements during the Caledonian orogeny.Verschure et al. (1980) found a similar stilpnomelane formation in adjacent terrains of the basement and proposed a weak Caledonian metamorphism of about 400 my.

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Résumé Les roches métamorphiques de la presqu'Île de Strand (sud-ouest de la Norvège) appartiennent à un empilement de nappes formées de roches pré-cambriennes et charriées vers le SSE sur le bouclier baltique au cours de l'orogenèse calédonienne (Sigmond Kildal 1978).Une nappe supérieure comprend des métagranites, des mélagabbroÏdes et des gneiss. Leurs paragenèses, du facies des granulites (âge du métamorphisme: 1,5 Ga) ont été rétromorphosées dans le facies des schistes verts il y a probablement 1,18 Ga. Cette nappe ne subsiste qu'en petits fragments épargnés par l'érosion.Une nappe inférieure est composée de roches métasédimentaires. Ces roches présentent des paragenèses du faciès supérieur des amphibolites, également rétromorphosées dans le facies des schistes verts. L'application du diagramme de Raase (1974) aux teneurs en Al^VI des amphiboles formées lors des deux processus métamorphiques indique que la rétromorphose s'est déroulée à une pression supérieure à celle du métamorphisme ancien. Un âge de 1,16 Ga sur roche totale semble indiquer que le mÊme processus orogénique a servi de cadre à la rétromorphose en facies des schistes verts dans les deux nappes.Du stilpnomélane, présent tant dans la nappe inférieure que dans le bouclier baltique autochtone, témoigne d'un métamorphisme calédonien (400 Ma) de faible degré.

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Strand ( ) , NNW (Sigmond KILDAL, 1978). , . - 1,5 , 118 , . . . , . Al^VI , , RAASE (1974) , , . 1,6 , , , . (400 ) , .

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Polymetamorphic relations in iron ores from the Iron Quadrangle,Brazil: The correlation of oxygen isotope variations with deformation history   总被引：2，自引：0，他引：2  

Joachim Hoefs  Georg Müller  Alfred K. Schuster 《Contributions to Mineralogy and Petrology》1982,79(3):241-251

This study deals with the oxygen isotope composition of hematite-rich ore bodies in the Iron Quadrangle, Brazil. The area studied can be divided into two different regions: a western (W) zone of greenschist facies assemblages and an eastern (E) zone of amphibolite facies with transitions into granulite facies assemblages.The ¹⁸O values of 136 quartz-iron oxide pairs have been determined and temperatures of formation have been calculated. The ¹⁸O values of quartz vary between +6 and 20 except one value near +23, whereas the iron oxides fall between –4 and +10, with nearly 80% of the iron oxide values between –0.5 and 4.0. The regional distribution of the ¹⁸O values is as follows: in the W-region 85% of the quartz are >12, whereas in the E-region only 46% fall in this range, In contrast to quartz the iron oxides do not show any regional differences.The variation of oxygen isotope fractionations between quartz and iron oxides is obviously related to the complex deformation history of the iron ores. Samples with a primary schistosity (S₁) only represent peak metamorphic conditions. In the E-region the (S₁) high temperatures >700° C seem to correspond to orogenic events in the Archaen basement 2,700 m.y. ago. In the W-region S₁-temperatures between 460° and 560° C seem to represent peak metamorphic conditions of the Proterozoic Minas metamorphism 2,000 m.y. ago. Iron ores which have been overprinted by later deformation events are selectively reset to lower isotopic temperatures. The more closely spaced the schistosity planes the larger the extent of a temperature lowering.The genetic processes associated with these hematite-rich ore bodies appear to be sedimentary-metamorphic rather than metasomatic processes. Furthermore, there is no evidence for secondary leaching by weathering solutions.  相似文献