Geological structure and indicators of hydrothermal ore-bearing activity at the junction of the southern rift segment and the Doldrums Transform Fracture Zone, Central Atlantic     

S. G. Skolotnev  A. A. Peive  V. Yu. Lavrushin  T. A. Demidova  S. S. Abramov  A. E. Eskin  D. I. Krinov  V. V. Petrova  N. V. Razdolina  N. N. Turko  N. V. Tsukanov  N. L. Chaplygina  E. V. Sharkov 《Doklady Earth Sciences》2006,407(2):361-365

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Two-stage metamorphic evolution of the Bemarivo Belt of northern Madagascar: constraints from reaction textures and in situ monazite dating     

N. JÖNS  V. SCHENK  P. APPEL  T. RAZAKAMANANA 《Journal of Metamorphic Geology》2006,24(4):329-347

New results on the pressure–temperature–time evolution, deduced from conventional geothermobarometry and in situ U‐Th‐total Pb dating of monazite, are presented for the Bemarivo Belt in northern Madagascar. The belt is subdivided into a northern part consisting of low‐grade metamorphic epicontinental series and a southern part made up of granulite facies metapelites. The prograde metamorphic stage of the latter unit is preserved by kyanite inclusions in garnet, which is in agreement with results of the garnet (core)‐alumosilicate‐quartz‐plagioclase (inclusions in garnet; GASP) equilibrium. The peak metamorphic stage is characterized by ultrahigh temperatures of ～900–950 °C and pressures of ～9 kbar, deduced from GASP equilibria and feldspar thermometry. In proximity to charnockite bodies, garnet‐sillimanite‐bearing metapelites contain aluminous orthopyroxene (max. 8.0 wt% Al₂O₃) pointing to even higher temperatures of ～970 °C. Peak metamorphism is followed by near‐isothermal decompression to pressures of 5–7 kbar and subsequent near‐isobaric cooling, which is demonstrated by the extensive late‐stage formation of cordierite around garnet. Internal textures and differences in chemistry of metapelitic monazite point to a polyphasic growth history. Monazite with magmatically zoned cores is rarely preserved, and gives an age of c. 737 ± 19 Ma, interpreted as the maximum age of sedimentation. Two metamorphic stages are dated: M1 monazite cores range from 563 ± 28 Ma to 532 ± 23 Ma, representing the collisional event, and M2 monazite rims (521 ± 25 Ma to 513 ± 14 Ma), interpreted as grown during peak metamorphic temperatures. These are among the youngest ages reported for high‐grade metamorphism in Madagascar, and are supposed to reflect the Pan‐African attachment of the Bemarivo Belt to the Gondwana supercontinent during its final amalgamation stage. In the course of this, the southern Bemarivo Belt was buried to a depth of >25 km. Approximately 25–30 Myr later, the rocks underwent heating, interpreted to be due to magmatic underplating, and uplift. Presumably, the northern part of the belt was also affected by this tectonism, but buried to a lower depth, and therefore metamorphosed to lower grades.  相似文献   

基于国际经验的西部经济发展与生态建设互动途径研究     

陈锋  延军平 《世界地理研究》2006,15(4):41-47

本文在分析巴西、印度等发展中国家和美国、德国等发达国家经济发展和生态环境建设经验的基础上,针对我国西部农村贫困和产业落后等影响经济、生态的制约因素,提出了西部经济发展与生态建设互动的一些有效途径,以期对最终实现西部经济发展与生态建设的双赢有所启示。  相似文献   

Powder factors in asymmetric blast patterns     

A. T. Spathis 《Fragblast: International Journal for Blasting and Fragmentation》2006,10(3):97-109

A cell powder factor defines the local powder factor in a simple geometric procedure that accounts for the charge in each blast hole and the triangulation formed by blast hole collars in a blast pattern. In the case of asymmetric blast patterns, the cell powder factor deviates from the global powder factor. Poor drilling of blast hole collars produces significant variation in the cell powder factor, more so, than does poor blast hole charging. The cell powder factor does not account for timing within a blast and does not easily handle non-parallel blast hole configurations. The cell powder factor is best used as a design or audit tool before blast holes are loaded. It gives the opportunity to correct for poor drilling and/or poor charging practices prior to firing a blast.  相似文献   

The structure and dynamics of 2-dimensional fluids in swelling clays   总被引：3，自引：0，他引：3  

Neal T. Skipper  Peter A. Lock  James O. Titiloye  Jan Swenson  Zakaria A. Mirza  W. Spencer Howells  Felix Fernandez-Alonso 《Chemical Geology》2006,230(3-4):182-196

The interlayer pores of swelling 2:1 clays provide an ideal 2-dimensional environment in which to study confined fluids. In this paper we discuss our understanding of the structure and dynamics of interlayer fluid species in expanded clays, based primarily on the outcome of recent molecular modelling and neutron scattering studies. Counterion solvation is compared with that measured in bulk solutions, and at a local level the cation-oxygen coordination is found to be remarkably similar in these two environments. However, for the monovalent ions the contribution to the first coordination shell from the clay surfaces increases with counterion radius. This gives rise to inner-sphere (surface) complexes in the case of potassium and caesium. In this context, the location of the negative clay surface charge (i.e. arising from octahedral or tetrahedral substitution) is also found to be of major importance. Divalent cations, such as calcium, eagerly solvate to form outer-sphere complexes. These complexes are able to pin adjacent clay layers together, and thereby prevent colloidal swelling. Confined water molecules form hydrogen bonds to each other and to the clays' surfaces. In this way their local environment relaxes to close to the bulk water structure within two molecular layers of the clay surface. Finally, we discuss the way in which the simple organic molecules methane, methanol and ethylene glycol behave in the interlayer region of hydrated clays. Quasi-elastic neutron scattering of isotopically labelled interlayer CH₃OD and (CH₂OD)₂ in deuterated clay allows us to measure the diffusion of the CH₃- and CH₂-groups in both clay and liquid environments. We find that in both the one-layer methanol solvates and the two-layer glycol solvates the diffusion of the most mobile organic molecules is close to that in the bulk solution.  相似文献   

Compositional trends among IID irons; their possible formation from the P-rich lower magma in a two-layer core     

John T. Wasson  Heinz Huber 《Geochimica et cosmochimica acta》2006,70(24):6153-6167

Group IID is the fifth largest group of iron meteorites and the fourth largest magmatic group (i.e., that formed by fractional crystallization). We report neutron-activation data for 19 (of 21 known) IID irons. These confirm earlier studies showing that the group has a relatively limited range in Ir concentrations, a factor of 5. This limited range is not mainly due to incomplete sampling; Instead, it seems to indicate low solid/liquid distribution coefficients reflecting very low S contents of the parental magma, the same explanation responsible for the limited range in group IVA. Despite this similarity, these two groups have very different volatile patterns. Group IVA has very low abundances of the volatile elements Ga, Sb and Ge whereas in group IID Ga and Sb abundances are the highest known in a magmatic group of iron meteorites and Ge abundances are the second highest (after group IIAB). Group IID appears to be the only large magmatic group having high volatile abundances but low S. In the volatile-depleted groups IVA and IVB it is plausible that S was lost as a volatile from a chondritic precursor material. Because group IID seems to have experienced minimal loss of volatiles, we suggest that S was lost as an early melt having a composition near that of the Fe–FeS eutectic (315 mg/g S). When temperatures had risen 400–500 K higher P-rich melts formed, became gravitationally unstable, and drained through the first melt to form an inner core that was parental to the IID irons. As discussed by [Kracher, A., Wasson, J.T., 1982. The role of S in the evolution of the parental cores of the iron meteorites. Geochim. Cosmochim. Acta 46, 2419–2426], it is plausible that a metal-rich inner core and a S-rich outer core could coexist metastably because stratification near the interface permitted only diffusional mixing. The initial liquidus temperature of the inner, P-rich core is estimated to have been 1740 K; after >60% crystallization the increase in P and the decrease in temperature may have permitted immiscibility with the S-rich outer core. We have not recognized samples of the outer core.  相似文献   

A reassessment of models for hydrocarbon generation in the Khibiny nepheline syenite complex, Kola Peninsula, Russia   总被引：2，自引：0，他引：2  

B. Beeskow  P.J. Treloar  A.H. Rankin  T.W. Vennemann  J. Spangenberg 《Lithos》2006,91(1-4):1-18

Although hydrocarbon-bearing fluids have been known from the alkaline igneous rocks of the Khibiny intrusion for many years, their origin remains enigmatic. A recently proposed model of post-magmatic hydrocarbon (HC) generation through Fischer-Tropsch (FT) type reactions suggests the hydration of Fe-bearing phases and release of H₂ which reacts with magmatically derived CO₂ to form CH₄ and higher HCs. However, new petrographic, microthermometric, laser Raman, bulk gas and isotope data are presented and discussed in the context of previously published work in order to reassess models of HC generation. The gas phase is dominated by CH₄ with only minor proportions of higher hydrocarbons. No remnants of the proposed primary CO₂-rich fluid are found in the complex. The majority of the fluid inclusions are of secondary nature and trapped in healed microfractures. This indicates a high fluid flux after magma crystallisation. Entrapment conditions for fluid inclusions are 450–550 °C at 2.8–4.5 kbar. These temperatures are too high for hydrocarbon gas generation through the FT reaction. Chemical analyses of rims of Fe-rich phases suggest that they are not the result of alteration but instead represent changes in magma composition during crystallisation. Furthermore, there is no clear relationship between the presence of Fe-rich minerals and the abundance of fluid inclusion planes (FIPs) as reported elsewhere. δ¹³C values for methane range from − 22.4‰ to − 5.4‰, confirming a largely abiogenic origin for the gas. The presence of primary CH₄-dominated fluid inclusions and melt inclusions, which contain a methane-rich gas phase, indicates a magmatic origin of the HCs. An increase in methane content, together with a decrease in δ¹³C isotope values towards the intrusion margin suggests that magmatically derived abiogenic hydrocarbons may have mixed with biogenic hydrocarbons derived from the surrounding country rocks.  相似文献   

Sulfide evolution in high-temperature to ultrahigh-temperature metamorphic rocks from Lützow–Holm Complex, East Antarctica     

T. Kawakami  D.J. Ellis  A.G. Christy 《Lithos》2006,92(3-4):431-446

The high-temperature (HT) to ultrahigh-temperature (UHT) metamorphic rocks from Lützow–Holm Complex, East Antarctica show a systematic difference between sulfide assemblages in the rock matrix and those found as inclusions in the silicates stable in high-temperatures. Matrix sulfides are commonly pyrite with or without pentlandite and chalcopyrite. On the other hand, inclusion sulfides are pyrrhotite with or without pentlandite and chalcopyrite lamellae. When recalculated into integrated single-phase sulfide compositions, inclusion sulfides from the UHT region showed a wider range of solid–solution composition than the inclusion sulfides from the HT region. The host minerals of the sulfides with extreme solid–solution compositions are those stable at the peak of metamorphism such as orthopyroxene and garnet. One of the most extreme ones is included in orthopyroxene coexisting with sillimanite ± quartz, which is the diagnostic mineral assemblage of UHT metamorphism. These observations suggest that sulfide inclusions preserve their peak metamorphic compositions. Pyrrhotite did not revert to pyrite because of the closed system behavior of sulfur in inclusion sulfides. On the other hand, in the rock matrix where the open system behavior of sulfur is permitted, original sulfides were partly to completely altered by the later fluid activity.  相似文献   

Zircon geochronology and Sm–Nd isotopic study: Further constraints for the Archean and Paleoproterozoic geodynamical evolution of the southeastern Guiana Shield, north of Amazonian Craton, Brazil     

Lúcia T. da Rosa-Costa  Jean M. Lafon  Claude Delor 《Gondwana Research》2006,10(3-4):277-300

The eastern part of the Guiana Shield, northern Amazonian Craton, in South America, represents a large orogenic belt developed during the Transamazonian orogenic cycle (2.26–1.95 Ga), which consists of extensive areas of Paleoproterozoic crust and two major Archean terranes: the Imataca Block, in Venezuela, and the here defined Amapá Block, in the north of Brazil.

Pb-evaporation on zircon and Sm–Nd on whole rock dating were provided on magmatic and metamorphic units from southwestern Amapá Block, in the Jari Domain, defining its long-lived evolution, marked by several stages of crustal accretion and crustal reworking. Magmatic activity occurred mainly at the Meso-Neoarchean transition (2.80–2.79 Ga) and during the Neoarchean (2.66–2.60 Ga). The main period of crust formation occurred during a protracted episode at the end of Paleoarchean and along the whole Mesoarchean (3.26–2.83 Ga). Conversely, crustal reworking processes have dominated in Neoarchean times. During the Transamazonian orogenic cycle, the main geodynamic processes were related to reworking of older Archean crust, with minor juvenile accretion at about 2.3 Ga, during an early orogenic phase. Transamazonian magmatism consisted of syn- to late-orogenic granitic pulses, which were dated at 2.22 Ga, 2.18 Ga and 2.05–2.03 Ga. Most of the ε_Nd values and T_DM model ages (2.52–2.45 Ga) indicate an origin of the Paleoproterozoic granites by mixing of juvenile Paleoproterozoic magmas with Archean components.

The Archean Amapá Block is limited in at southwest by the Carecuru Domain, a granitoid-greenstone terrane that had a geodynamic evolution mainly during the Paleoproterozoic, related to the Transamazonian orogenic cycle. In this latter domain, a widespread calc-alkaline magmatism occurred at 2.19–2.18 Ga and at 2.15–2.14 Ga, and granitic magmatism was dated at 2.10 Ga. Crustal accretion was recognized at about 2.28 Ga, in agreement with the predominantly Rhyacian crust-forming pattern of the eastern Guiana Shield. Nevertheless, T_DM model ages (2.50–2.38 Ga), preferentially interpreted as mixed ages, and ε_Nd < 0, point to some participation of Archean components in the source of the Paleoproterozoic rocks. In addition, the Carecuru Domain contains an oval-shaped Archean granulitic nucleus, named Paru Domain. In this domain, Neoarchean magmatism at about 2.60 Ga was produced by reworking of Mesoarchean crust, as registered in the Amapá Block. Crustal accretion events and calc-alkaline magmatism are recognized at 2.32 Ga and at 2.15 Ga, respectively, as well as charnockitic magmatism at 2.07 Ga.

The lithological association and the available isotopic data registered in the Carecuru Domain suggests a geodynamic evolution model based on the development of a magmatic arc system during the Transamazonian orogenic cycle, which was accreted to the southwestern border of the Archean Amapá Block.  相似文献   

Microvariability of line profiles in the spectrum of the star ι Her     

A. F. Kholtygin  G. A. Galazutdinov  T. E. Burlakova  G. G. Valyavin  S. N. Fabrika  B. -C. Lee 《Astronomy Reports》2006,50(3):220-231

We present the results of a search for and analysis of line-profile variations in the spectrum of the star ι Her. The observations were acquired with the 1.8 m telescope of the Bohyunsan Optical Astronomy Observatory (Republic of Korea) in May–June 2004. We obtained 69 spectra of the star with signal-to-noise ratios ≈300 and a time resolution of 5–7 min. Profile variability was revealed for six lines of HI, HeI, and SiIII, in the central parts of the lines. The variability amplitude is ≈(1–2)% in units of the intensity of the adjacent continuum. Evidence was found for cyclic variations of the lines, with periods from ≈7^h to ≈2.9^d. We conclude that ι Her belongs to the group of slowly pulsating stars.  相似文献