The isotopic composition and elemental abundance of lutetium in meteorites and terrestrial samples and the ¹⁷⁶Lu cosmochronometer     

M.T. McCulloch  J.R. De Laeter  K.J.R. Rosman 《Earth and Planetary Science Letters》1976,28(3):308-322

The isotopic composition of lutetium has been measured in a range of terrestrial and meteoritic materials using solid-source mass spectrometric techniques. The meteoritic and terrestrial isotopic abundances are identical within experimental errors. The absolute ¹⁷⁵Lu/¹⁷⁶Lu ratio as determined in this work is 37.36 ± 0.07 at the 95% confidence level. On the basis of this measurement the atomic weight of lutetium has been calculated to be 174.967 ± 0.002, which is in good agreement with the currently accepted figure of 174.97 ± 0.01.Using the stable isotope dilution technique the abundance of lutetium has been determined in 25 stone, 1 stony-iron and 8 iron meteorites, and in 12 standard rocks, with an accuracy of ±5% at the 95% confidence level. In general, there is good agreement between this work and other published data.The ¹⁷⁶Lu-¹⁷⁶Hf pair has been proposed as an s process nucleocosmochronometer, because of the long half-life of ¹⁷⁶Lu and the unique fact that both are s process isobars. The isotopic and elemental abundances of lutetium as measured in this work have been used with published nuclear data to estimate the mean age of s process nucleosynthesis for this isobaric pair, using the Schramm-Wasserburg formalism. The mean age cannot be accurately determined at the present time because of the lack of 30 keV neutron capture cross-section data for s only process nuclides and an accurate measurement of the branching ratio of ¹⁷⁵Lu + n. However, it is possible to place constraints on the nuclear parameters in this mass region using a reasonable s process chronology based on the decay of ¹⁷⁶Lu.  相似文献   

A rationale for the origins of massif anorthosites     

Graham Ryder 《Lithos》1974,7(3):139-146

The origin of massif anorthosites cannot be simply explained by a single magma type. Two of the commonly proposed parents for anorthosites are andesites (quartz-diorites) and high-alumina basalts. It is proposed here that these two magmas are the parents for two groups of anorthosites which include all anorthosite massifs, and that the parents for any given anorthosite massif can be determined by the rock sequence associated with the massif.Evidence from experiments and from phenocrysts in volcanics, suggests that andesites crystallizing in the granulite facies would produce plagioclase cumulates (anorthosites) at the base, followed by dioritic and acidic material, whereas high-alumina basalts would produce gabbros followed by anorthosite with very little succeeding acidic material. All massif anorthosites for which relevant data is available have one or the other of these stratigraphic sequences. Grouped according to these sequences, they coincide with two previously proposed groups, i.e. Andesine-type and Labradorite-type, whose characteristics are shown to be compatible with derivation from andesite and high-alumina basalt, respectively.  相似文献   

Resolved spectroscopy of a gravitationally lensed L* Lyman-break galaxy at z∼ 5     

A. M. Swinbank  R. G. Bower  Graham P. Smith  R. J. Wilman  Ian Smail  R. S. Ellis  S. L. Morris  J.-P. Kneib 《Monthly notices of the Royal Astronomical Society》2007,376(2):479-491

  相似文献   

Intracluster light and the extended stellar envelopes of cD galaxies: an analytical description     

Marc S. Seigar †  Alister W. Graham  Helmut Jerjen 《Monthly notices of the Royal Astronomical Society》2007,378(4):1575-1588

  相似文献   

An alternative to common envelope evolution     

Martin E. Beer  Lynnette M. Dray  rew R. King  Graham A. Wynn 《Monthly notices of the Royal Astronomical Society》2007,375(3):1000-1008

  相似文献   

Sieve‐bucket for rapid field separation of macrofauna from bottom samples (note)     

Alan A. Graham  Carolyn W. Burns 《新西兰海洋与淡水研究杂志》2013,47(3):609-611

A lidded, 18‐litre sieve bucket was used to separate benthic macroinvertebrates from samples of mud taken with an Ekman grab. The device is operated in shallow water near the shore, and an entire Ekman grab sample (up to 10 litres) can be sieved in 5–10 min.  相似文献   

Hooker's sea lions in southern New Zealand     

Graham J. Wilson 《新西兰海洋与淡水研究杂志》2013,47(3):373-375

The discovery at Stewart Island of a hauling‐out ground regularly used by Hooker's sea lions (Phocarctos hooked) is described, and recent sightings of sea lions in southern New Zealand are reported. An attempted copulation between a male Hooker's sea lion and a dead female fur seal (Arctocephalus forsteri) is also described.  相似文献   

Evidence for distinct proportions of subducted oceanic crust and lithosphere in HIMU-type mantle beneath El Hierro and La Palma, Canary Islands     

James M.D. Day  D. Graham Pearson  David Lowry 《Geochimica et cosmochimica acta》2010,74(22):6565-6589

Shield-stage high-MgO alkalic lavas from La Palma and El Hierro (Canary Islands) have been characterized for their O-Sr-Nd-Os-Pb isotope compositions and major-, trace-, and highly siderophile-element (HSE: Os, Ir, Ru, Pt, Pd, Re) abundances. New data are also reported for associated evolved rocks, and entrained xenoliths. Clear differences in Pd/Ir and isotopic ratios for high Os (>50 ppt) lavas from El Hierro (δ¹⁸O_olivine = 5.17 ± 0.08‰; ⁸⁷Sr/⁸⁶Sr = 0.7029 to 0.7031; ε_Nd = +5.7 to +7.1; ¹⁸⁷Os/¹⁸⁸Os = 0.1481 to 0.1750; ²⁰⁶Pb/²⁰⁴Pb = 19.1 to 19.7; Pd/Ir = 6 ± 3) versus those from La Palma (δ¹⁸O_olivine = 4.87 ± 0.18‰; ⁸⁷Sr/⁸⁶Sr = 0.7031 to 0.7032; ε_Nd = +5.0 to +6.4; ¹⁸⁷Os/¹⁸⁸Os = 0.1421 to 0.1460; ²⁰⁶Pb/²⁰⁴Pb = 19.5 to 20.2; Pd/Ir = 11 ± 4) are revealed from the dataset.Crustal or lithospheric assimilation during magma transport cannot explain variations in isotopic ratios or element abundances of the lavas. Shallow-level crystal-liquid fractionation of olivine, clinopyroxene and associated early-crystallizing minerals (e.g., spinel and HSE-rich phases) controlled compatible element and HSE abundances; there is also evidence for sub-aerial degassing of rhenium. High-MgO lavas are enriched in light rare earth elements, Nb, Ta, U, Th, and depleted in K and Pb, relative to primitive mantle abundance estimates, typical of HIMU-type oceanic island basalts. Trace element abundances and ratios are consistent with low degrees (2-6%) of partial melting of an enriched mantle source, commencing in the garnet stability field (?110 km). Western Canary Island lavas were sulphur undersaturated with estimated parental melt HSE abundances (in ppb) of 0.07 ± 0.05 Os, 0.17 ± 0.16 Ir, 0.34 ± 0.32 Ru, 2.6 ± 2.5 Pt, 1.4 ± 1.2 Pd, 0.39 ± 0.30 Re. These estimates indicate that Canary Island alkali basalts have lower Os, Ir and Ru, but similar Pt, Pd and Re contents to Hawai’ian tholeiites.The HIMU affinities of the lavas, in conjunction with the low δ¹⁸O_olivine and high ²⁰⁶Pb/²⁰⁴Pb for La Palma, and elevated ¹⁸⁷Os/¹⁸⁸Os for El Hierro implies melting of different proportions of recycled oceanic crust and lithosphere. Our preferred model to explain isotopic differences between the islands is generation from peridotitic mantle metasomatised by <10% pyroxenite/eclogite made from variable portions of similar aged recycled oceanic crust and lithosphere. The correspondence of radiogenic ²⁰⁶Pb/²⁰⁴Pb, ¹⁸⁷Os/¹⁸⁸Os, elevated Re/Os and Pt/Os, and low-δ¹⁸O in western Canary Island lavas provides powerful support for recycled oceanic crust and lithosphere to generate the spectrum of HIMU-type ocean island basalt signatures. Persistence of geochemical heterogeneities throughout the stratigraphies of El Hierro and La Palma demonstrate long-term preservation of these recycled components in their mantle sources over relatively short-length scales (∼50 km).  相似文献   

The geochemistry of primary and weathered oil shale and coquina across the Julia Creek vanadium deposit (Queensland, Australia)     

Stephen Edward Lewis  Robert A. Henderson  Gerald R. Dickens  Graham A. Shields  Simon Coxhell 《Mineralium Deposita》2010,45(6):599-620

A significant resource of vanadium and molybdenum exists near Julia Creek, Australia, where the middle Cretaceous organic-rich Toolebuc Formation lies between 0 and 25 m of the surface. We present and discuss a comprehensive geochemical study of the Toolebuc Formation and its enclosing stratigraphy near Julia Creek to understand this ore deposit. V and Mo contents in fresh facies are strongly associated with total organic carbon (TOC) contents, but not with Al or CaCO₃; this suggests that V and Mo were originally concentrated in the organic fraction. However, chemical extractions using H₂O₂ indicate that Mo was originally concentrated in pyrite. The data also suggest that V was mobilised from organic matter during early diagenesis and became associated with clays as little V was extracted by H₂O₂ in the fresh samples. TOC contents in the Toolebuc Formation were removed during weathering, residually enriching trace metals including V and Mo, and as a result, the TOC relationship with V and Mo disintegrates. With weathering, both V and Mo predominantly became associated with iron oxide/hydroxide phases (and possibly other unidentified phases) as these elements in the weathered facies were highly soluble in the sodium citrate–sodium dithionite digestion. Large shale-hosted V and Mo deposits such as Julia Creek offer a potentially viable alternative to the currently mined magnetite-hosted deposits. A thorough understanding of the formation and host mineral phases for V and Mo of these shale deposits, however, is critical to ensure that these valuable metals can be feasibly extracted.  相似文献   

A major element,PGE and Re–Os isotope study of Middle Atlas (Morocco) peridotite xenoliths: Evidence for coupled introduction of metasomatic sulphides and clinopyroxene     

Nadine Wittig  D. Graham Pearson  Joel A. Baker  Svend Duggen  Kaj Hoernle 《Lithos》2010,115(1-4):15-26

We present major element and PGE (platinum-group-element) abundances in addition to Re–Os isotope data for 11 spinel-facies whole rock peridotites from a single maar from the Middle Atlas Mountains, Morocco.Major element systematics of these xenoliths are generally correlated with indices of depletion. FeO–MgO systematics appear to suggest spinel-facies melting in the range of 5 to 25%. However, Al₂O₃ abundances in these xenoliths appear elevated relative to primitive mantle (Prima). The Al₂O₃ abundances in conjunction with other major elements require distinct re-enrichment of the Middle Atlas continental mantle root due to melt/rock reaction and precipitation of amphibole and/or clinopyroxene from passing silicate melts akin to MORB or OIB that evolved in reverse direction along the melting curves in e.g. FeO–MgO space. Sc and V confirm the range of apparent depletion and also indicate that the currently preserved fO₂ in these peridotites is distinctly different from fO₂ conditions observed in subduction zones.The majority of these xenoliths have low Os and Ir (I-PGEs) concentrations relative to Prima and modelled sulphide- and clinopyroxene-depleted residues of mantle melting under low fO₂, mid-ocean ridge-like conditions. Moreover, Pt and Pd (P-PGE) abundances are elevated when compared to their expected abundances after substantial melt extraction. Importantly, the systematically low Ir abundances in the majority of samples show well-correlated trends with Al₂O₃, MgO and Cu that are inconsistent with established melting trends. Os isotopes in the Middle Atlas xenoliths range from ¹⁸⁷Os/¹⁸⁸Os = 0.11604 to 0.12664 although most samples are close to chondritic. The Os isotope ratios are decoupled from ¹⁸⁷Re/¹⁸⁸Os but, together with Re abundances, also exhibit a good correlation with Al₂O₃, MgO and Cu.The major element, I-PGE and Os isotope correlations suggest that the initial melt depletion led to the exhaustion of sulphide and clinopyroxene (20 to 30%) without significant stabilization of I-PGE-rich alloys. During later modal metasomatism of the refractory Middle Atlas continental mantle root with silicate melts akin to MORB or OIB the introduction of clinopyroxene/amphibole reduced the volume of the melt inducing sulphur saturation in these melts causing precipitation of secondary sulphides. This coupled crystallization of pyroxenes and sulphides (chalcopyrite) resulted in the two-component mixing systematics exhibited by I-PGEs, Os isotopes with major elements and Cu preserved in the Middle Atlas continental mantle root.  相似文献