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1.
A trace fossil, Centrichnus eccentricus, was found beneath a saddle oyster (Anomia ephippium) that was preserved undisturbed on its substratum (a shell of Pecten jacobaeus), at the site of attachment of the calcified byssus. 相似文献
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Investigations on S, C, O, Sr, and Pb isotopes in ores, gangue, and country rocks of the Chaudfontaine ore deposit confirm that interbedded barite and white sparry calcites are cogenetic. They emphasize the marine origin of S and the nonmarine origin of the metals. They underline the important role played by the bacterial reduction at the site of deposition. Hypotheses concerning the source of the metals and the nature of the brines involved in their transportation are briefly discussed. 相似文献
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The skarn complex of Traversella was formed at the expense of various rock types (calcic hornfels, gneiss, dolomitic marble)
occurring in the contact aureole of the dioritic intrusion of Traversella (30±5 Ma). Application of phase equilibria has fixed
the temperature of the primary stage of skarn formation between 550° C to 625° C. Similar applications indicate a larger range
of temperature (525° C to 300° C) for the secondary stage. The different types of skarn (primary stage) are enriched in REE
relative to the corresponding precursor rock (T.R.=126 ppm (protolith) to 228 ppm (inner zone) for the skarn on gneisses;
T.R.=14 ppm to 71 ppm for the skarn on calcic hornfelses; T.R.=12 ppm to 200 ppm for the skarn on dolomitic marbles), but
all the inner zones of these different types of skarn show a similar REE distribution with a slight LREE fractionation and
no Eu anomaly. It is inferred that the primary metasomatic fluid has a parallel REE pattern. The oxygen isotope composition
of water in equilibrium with the early stage of skarn at T=600° C ranges from 8.3 per mil to 8.9 per mil. At the beginning of the first hydroxylation stage (secondary stage), the fluid
σ
18O remains in the range observed in the primary stage but within it, there is a sharp decrease from 8.0 per mil to 5.0 per
mil. During the sulphidation stage, the fluid σ
18O decreases more gradually from 5.0 per mil to 3.0 per mil. The I
Sr of the early skarn silicates ranges from the values observed in the dolomitic marbles (0.70874 to 0.70971) to the I
Sr of the intrusion (0.70947 to 0.71064). During the secondary stage, there is a progressive increase of the minerals I
Sr up to 0.71372. The REE pattern of the primary metasomatic fluid does not put any precise constraint on the primary fluid
source. On the other hand, both stable and radiogenic isotopes suggest that the early high-temperature metasomatic fluid was
isotopically equilibrated with the dioritic intrusion. This implies that this early fluid is either exsolved from the crystallizing
intrusion or a metamorphic water previously equilibrated with the intrusion. During the secondary stage, the replacement of
the early anhydrous phases by hydrated parageneses is accompanied by the mixing with meteoric fluid as indicated by stable
(σ
18O) and radiogenic (87Sr/86Sr) isotopes. 相似文献
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~(40)Ar-~(39)Ar GEOCHRONOLOGY OF THE SUTURE ZONE, LADAKH, INDIA1 TalatAhmedetal.GeochemicalJournal,1999.
2 HoneggerK ,etal.EarthandPlanetaryScienceLetters,1982 ,6 0 :2 53.
3 SearleMP ,etal.GeologicalSocietyofAmericaBulletin ,1987,98:6 78.
4 SharmaK ,K .PhysicsandChemistryoftheEarth ,1990 ,17( 2 ) :133.
5 Venkatesan ,etal.EarthandPlanetSciLett,1993,119:181.… 相似文献
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Water samples from eight major Texas rivers were collected at different times during 1997–1998 to determine the dissolved and particulate trace metal concentrations, expected to show differences in climate patterns, river discharge and other hydrochemical conditions, and human activities along the different rivers. Specifically, two eastern Texas rivers (Sabine, Neches) lie in a region with high vegetation, flat topography, and high rainfall rates, while four Central Texas rivers (Trinity, Brazos, Colorado, and San Antonio) flow through large population centers. Relatively high dissolved organic carbon (DOC) concentrations in the eastern Texas rivers and lower pH led to higher Fe and Mn concentrations in river waters. The rivers that flow through large population centers showed elevated trace metal (e.g., Cd, Pb, Zn) concentrations partly due to anthropogenically produced organic ligands such as ethylenediaminetetraacetic acid (EDTA) present in these rivers. Trace metal levels were reduced below dams/reservoirs along several Texas rivers. Statistical analysis revealed four major factors (suspended particulate matter [SPM], EDTA, pH, and DOC) that can explain most of the observed variability of trace metal concentrations in these rivers. SPM concentrations directly controlled particulate metal contents. Variation in pH correlated with changes of dissolved Co, Fe, Mn, and Ni, and particulate Mn concentrations, while DOC concentrations were significantly related to dissolved Fe concentrations. Most importantly, it was found that, more than pH, EDTA concentrations exerted a major control on dissolved concentrations of Cd and Zn, and, to a lesser extent, Cu, Ni, and Pb. 相似文献
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Zusammenfassung Die chemische Analyse des neuen Minerals Johillerit mit der Elektronenmikrosonde ergab: Na2O 5,4, MgO 18,3, ZnO 5,4, CuO 15,8 und As2O5 55,8, Summe 100.7%. Aus diesem Ergebnis wurde die idealisierte Formel Na(Mg, Zn)3 Cu(AsO4)3 abgeleitet. Johillerit ist monoklin mit der RaumgruppeC2/c. Die Gitterkonstanten sind:a=11,870 (3),b=12,755 (3),c=6,770 (2) , =113,42 (2)°,Z=4. Die stärksten Linien des Pulverdiagramms sind: 4,06 (5) (22
), 3,50 (4) (310), 3,25 (8) (11
), 2,75 (10) (330, 240), 2,64 (5) (311, 13
, 40
), 1,952 (4) (13
, 35
), 1,682 (4) (20
, 460), 1,660 (5) (40
, 71
, 550, 64
), 1,522 (4) (442, 153, 13
). Es bestehen enge strukturelle Beziehungen zwischen Johillerit und O'Danielit, Na(Zn, Mg)3H2(AsO4)3, sowie einigen synthetischen. Verbindungen.Johillerit ist violett durchscheinend. Die Spaltbarkeit nach {010} ist ausgezeichnet und nach {100} und {001} gut.H (Mohs)3.D=4,15 undD
X
=4,21 g·cm–3. Das Mineral ist optisch zweiachsig positiv, 2V80 (5)°. Die Werte der Lichtbrechung sindn
=1,715 (4),n
=1,743 (4) undn
=1,783 (4). Die Auslöschung istn
b und auf (010)n
c16°. Johillerit ist stark pleochroitisch mit den AchsenfarbenX=violett-rot,Y = blauviolett undZ = grünblau. Das neue Mineral kommt in radialstrahligen Massen gemeinsam mit kupferhaltigem Adamin und Konichalcit in zersetzem Kupfererz von Tsumeb, Namibia, vor. Die Benennung erfolgte nach Prof. Dr.J.-E. Hiller (1911–1972).
Mit 1 Abbildung 相似文献
Johillerite, Na(Mg, Zn) 3 Cu(AsO 4 ) 3 , a new mineral from Tsumeb, Namibia
Summary Electron microprobe analysis of the new mineral johillerite gave Na2O 5.4, MgO 18.3, ZnO 5.4, CuO 15.8, and As2O5 55.8, total 100.7%. From this result, the ideal formula is given as Na(Mg, Zn)3 Cu(AsO4)3. Johillerite crystallizes monoclinic,C2/c. The unit cell dimensions are:a=11.870(3),b=12.755 (3),c=6.770 (2) , =113.42 (2)°,Z=4. The strongest lines on the X-ray powder diffraction pattern are: 4,06 (5) (22 ), 3,50 (4) (310), 3,25 (8) (11 ), 2,75 (10) (330, 240), 2,64 (5) (311, 13 , 40 ), 1,952 (4) (13 , 35 ), 1,682 (4) (20 , 460), 1,660 (5) (40 , 71 , 550, 64 ), 1,522 (4) (442, 153, 13 ). There is a close relationship between johillerite, o'danielite, Na(Zn, Mg)3H2(AsO4)3, and some synthetic compounds. Johillerite is violet in colour, transparent. Cleavage is {010} perfect, {100} and {001} good.H (Mohs)3.D=4.15 andD X =4.21 g·cm–3. The mineral is optically biaxial positive, 2V80 (5)°. The refractive indices are:n =1.715 (4),n =1.743 (4),n =1.783 (4). The extinction isn b and on (010)n c16°. Strongly pleochroic with axial coloursX=violet-red,Y=bluish violet andZ=greenish blue. The new mineral was found in radiated masses together with cuprian adamite and conichalcite in an oxidized copper ore from Tsumeb, Namibia. It is named in honour of Prof. Dr.J.-E. Hiller (1911–1972).
Mit 1 Abbildung 相似文献
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Mariusz A. Salamon 《Swiss Journal of Geoscience》2009,102(1):77-88
Valanginian strata in central epicratonic Poland have recently yielded crinoids, not previously recorded from the area. The fauna comprises isocrinids (Balanocrinus subteres, B. gillieroni, “Isocrinus?” lissajouxi), millericrinids (Apiocrinites sp.) and comatulids (Comatulida indet.). For comparison, a few samples of isocrinids from Valanginian strata of Hungary (Tethyan province) were also analysed. The isocrinids, cyrtocrinids and roveacrinids (sensu Rasmussen 1978 inclusive of Saccocoma sp.) were already known from the Valanginian of the southernmost Tethyan regions of Poland (Pieniny Klippen Belt and Tatra Mountains). The current study demonstrates their occurrence in central epicratonic Poland, and suggests that many Jurassic to Cretaceous stalked crinoid taxa (mainly isocrinids) predominated in the shallow-water settings of this area. Thus, the hypothesis of migration (at least from mid-Cretaceous onwards) to deep-water areas, as a response to an increase of the number of predators during the Mesozoic marine revolution, seems not to be universally applicable. 相似文献
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L. Melluso P. Censi G. Perini L. Vasconcelos V. Morra F. Guerreiro L. Bennio 《Mineralogy and Petrology》2004,80(3-4):201-213
Summary The Xiluvo complex of central Mozambique is made up of coarse- to fine-grained calciocarbonatites (sövites and alvikites), heavily altered lamprophyres and syenitic rocks that intruded the Precambrian basement ca. 120Ma ago. The carbonatites have fractionated rare earth element patterns (chondrite-normalized La/Yb=30–80) and markedly negative Rb, K, P, Zr and Ti anomalies in mantle-normalized incompatible element diagrams. The 18O (+7 to +8), 13C (–5), and the age-corrected 87Sr/86Sr (0.7032–0.7033) and 143Nd/144Nd (0.51263–0.51262) indicate an origin in the mantle. A few carbonatitic samples have higher 18O (+13), indicating interaction with high-18O crust or late-stage fluids. The chemical and isotopic compositions of the Xiluvo carbonatites and nearby carbonatites of similar age in Malawi indicate very similar sources, characterized by time-integrated depletion of Rb with respect to Sr and of Sm with respect to Nd. These characteristics point to a source similar in many respects to those of other East African carbonatites and to those of some ocean island basalts, with the additional influx of components possibly located in the African lithospheric mantle. 相似文献
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本文记述的掘足类(Scaphopods)系我国首次报道,化石产自西藏南部聂拉木县古错村北山下白垩统古错Ⅱ组中。计1属2种Dentalium jeffereysi Gardner,D.gucuoensis(sp.nov.). 相似文献
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Vinciennite and Cu-excess tennantite from the Layo (Cu,Sn, As,Au) epithermal deposit (Southern Peru)
Summary The Layo epithermal deposit, cutting Miocene-Pliocene calc-alkaline volcanites of the Tacaza group, includes a well-developed eastern zone (Vetas 7 and 8) in which brecciated and banded textures are associated with a large, intensely argillized zone containing diaspore and alunite. The vetas contain a typical Cu-As mineralogy of the acid-sulfate type (pyrite, enargite, Cu-excess tennantite, chalcopyrite, covellite) with an associated original stanniferous paragenesis including vinciennite and mawsonite. The vinciennite is close to the ideal end-member (Cu10Fe4SnAsS16) and the Cu-excess tennantite (Cu11FeAs4S13) shows a total absence of Zn and Ag; its very specific chemical composition suggests that all the iron is Fe3+, equilibrated by Cu+ and probably minor Cu2+.This particular mineralogical association implies deposition at relatively low temperature (300°C) and high aS2 (10–6.5 decreasing to 10–8.5), from a Cu-S-rich and Fe-Zn-poor fluid. The acid-sulfate epithermal mineralization of the eastern vetas of Layo appears to have preceded an adularia-sericite epithermal mineralization expressed in the western vetas of Layo and also in the nearby large epithermal veins at Orcopampa and Shila. It also supports the genetic relationship that is commonly evoked between porphyry copper and epithermal deposits.
With 10 Figures 相似文献
Le minéralogie originale à vinciente et tennantite riche du gisement épithermal (Cu, Sn, As, Au) de Layo (Sud Péru)
Résumé Le gîte épithermal de Layo est encaissé dans les volcanites calco-alcalines Miocène-Pliocène du groupe de Tacaza. Sa zone orientale renferme des corps minéralisés (Vetas 7 et 8) bien développés, à textures bréchiques et rubanées associées à une large zone intensément argilisée contenant diaspore et alunite.Les vetas présentent une association minéralogique à As-Cu typique des gisements acide-sulfate (pyrite, énargite, tennantite riche en cuivre, chalcopyrite, covellite) et une paragenèse stannifère originale renfermant vinciennite et mawsonite. La vinciennite est proche du pôle théorique (Cu10Fe4SnAsS16) et la tennantite riche en Cu (Cu11FeAs4S13) est dépourvue de Zn et de Ag; sa composition chimique suggère que tout le fer se présente sous la forme Fe3+, en équilibre avec Cu+, avec probablement une participation mineure de Cu2+.Cette association minéralogique particulière implique une mise en place sous forte fugacité en soufre (aS2 = 10–6.5 décroissant jusqu'à 10–8.5) à une température relativement basse de l'ordre de 300°C à partir d'un fluide riche en Cu et S et pauvre en Fe et Zn. La minéralisation de type acide-sulfate des vetas orientales de Layo précéderait celles de type adulaire-sericite des vetas occidentales de Layo et des gisements voisins de Orcopampa et Shila. Elle contribue à renforcer le lien fréquemment évoqué entre les porphyres cuprifères et les gisements épithermaux.
With 10 Figures 相似文献
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