Problems in data compilation     

Heinrich Eichhorn  Carl S. Cole 《Celestial Mechanics and Dynamical Astronomy》1985,37(3):263-275

Concepts involved in the estimation of target quantities and other adjustment parameters are critically discussd. We point out that one can find more accurate precepts for the reduction of data by utilizing all available constraints on all available data in the derivation of the reduction precepts. We introduce a measure for theefficiency of a set of adjustment parameters such that adjustments carried out using different precepts can be objectively compared. Finally, having applied our suggestions to a specific problem, we show that we have obtained estimates of a set of target quantities (in our case, star positions and proper motions) which have smaller formal errors than estimates of the same target quantities derived from the same input material but following traditional procedures.  相似文献   

Microdistribution of primordial Ne and Ar in fine‐grained rims,matrices, and dark inclusions of unequilibrated chondrites—Clues on nebular processes     

Nadia VOGEL  Rainer WIELER  Addi BISCHOFF  Heinrich BAUR 《Meteoritics & planetary science》2003,38(9):1399-1418

Abstract— The low temperature fine‐grained material in unequilibrated chondrites, which occurs as matrix, rims, and dark inclusions, carries information about the solar nebula and the earliest stages of planetesimal accretion. The microdistribution of primordial noble gases among these components helps to reveal their accretionary and alteration histories. We measured the Ne and Ar isotopic ratios and concentrations of small samples of matrix, rims, and dark inclusions from the unequilibrated carbonaceous chondrites Allende (CV3), Leoville (CV3), and Renazzo (CR2) and from the ordinary chondrites Semarkona (LL3.0), Bishunpur (LL3.1), and Krymka (LL3.1) to decipher their genetic relationships. The primordial noble gas concentrations of Semarkona, and—with certain restrictions—also of Leoville, Bishunpur, and Allende decrease from rims to matrices. This indicates a progressive accretion of nebular dust from regions with decreasing noble gas contents and cannot be explained by a formation of the rims on parent bodies. The decrease is probably due to dilution of the noble‐gas‐carrying phases with noble‐gas‐poor material in the nebula. Krymka and Renazzo both show an increase of primordial noble gas concentrations from rims to matrices. In the case of Krymka, this indicates the admixture of noble gas‐rich dust to the nebular region from which first rims and then matrix accreted. This also explains the increase of the primordial elemental ratio 36Ar/ 20Ne from rims to matrix. Larger clasts of the noble‐gas‐rich dust form macroscopic dark inclusions in this meteorite, which seem to represent unusually pristine material. The interpretation of the Renazzo data is ambiguous. Rims could have formed by aqueous alteration of matrix or—as in the case of Krymka—by progressive admixture of noble gas‐rich dust to the reservoir from which the Renazzo constituents accreted. The Leoville and Krymka dark inclusions, as well as one dark inclusion of Allende, show noble gas signatures different from those of the respective host meteorites. The Allende dark inclusion probably accreted from the same region as Allende rims and matrix but suffered a higher degree of alteration. The Leoville and Krymka dark inclusions must have accreted from regions different from those of their respective rims and matrices and were later incorporated into their host meteorites. The noble gas data imply a heterogeneous reservoir with respect to its primordial noble gas content in the accretion region of the studied meteorites. Further studies will have to decide whether these differences are primary or evolved from an originally uniform reservoir.  相似文献   

Hydrobiologische Untersuchungen an den hochalpinen Seen des San Bernardinopasses     

Heinrich Wolff 《Aquatic Sciences - Research Across Boundaries》1948,10(4):101-244

Ohne Zusammenfassung Ausgeführt und herausgegeben mit Unterstützung der ?Georges und Antoine Claraz-Schenkung instituta et curata Johannis Schinz Professoris auspiciis?  相似文献   

Fluid and source magma evolution of the Questa porphyry Mo deposit,New Mexico,USA   总被引：14，自引：1，他引：13  

Leonhard M. Klemm  Thomas Pettke  Christoph A. Heinrich 《Mineralium Deposita》2008,43(5):533-552

Combined fluid inclusion microthermometry and microanalysis by laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS) are used to constrain the hydrothermal processes forming a typical Climax-type porphyry Mo deposit. Molybdenum mineralisation at Questa occurred in two superimposed hydrothermal stages, a magmatic-hydrothermal breccia and later stockwork veining. In both stages, texturally earliest fluids were single-phase, of low salinity (~7 wt.% NaCl_equiv.) and intermediate-density. Upon decompression to ~300 bar, they boiled off a vapour phase, leaving behind a residual brine (up to 45 wt.% NaCl_equiv) at temperatures of ~420°C. The highest average Mo concentrations in this hot brine were ~500 μg/g, exceeding the Mo content of the intermediate-density input fluid by about an order of magnitude and reflecting pre-concentration of Mo by fluid phase separation prior to MoS₂ deposition from the brine. Molybdenum concentrations in brine inclusions, then, decrease down to 5 μg/g, recording Mo precipitation in response to cooling of the saline liquid to ~360°C. Molybdenite precipitation from a dense, residual and probably sulphide-depleted brine is proposed to explain the tabular shape of the ore body and the absence of Cu-Fe sulphides in contrast to the more common Cu-Mo deposits related to porphyry stocks. Cesium and Rb concentrations in the single-phase fluids of the breccia range from 2 to 8 and from 40 to 65 μg/g, respectively. In the stockwork veins, Cs and Rb concentrations are significantly higher (45–90 and 110–230 μg/g, respectively). Because Cs and Rb are incompatible and hydrothermally non-reactive elements, the systematic increase in their concentration requires two distinct pulses of fluid exsolution from a progressively more fractionated magma. By contrast, major element and ore metal concentrations of these two fluid pulses remain essentially constant. Mass balance calculations using fluid chemical data from LA-ICPMS suggest that at least 25 km³ of melt and 7 Gt of deep input fluid were necessary to provide the amount of Mo contained in the stockwork vein stage alone. While the absolute amounts of fluid and melt are uncertain, the well-constrained element ratios in the fluids together with empirical fluid/melt partition coefficients derived from the inclusion analyses suggest a high water content of the source melt of ~10%. In line with other circumstantial evidence, these results suggest that initial fluid exsolution may have occurred at a confining pressure exceeding 5 kbar. The source of the molybdenum-mineralising fluids probably was a particularly large magma chamber that crystallised and fractionated in the lower crust or at mid-crustal level, well below the shallow intrusions immediately underlying Questa and other porphyry molybdenum deposits. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

Shale basins,sulfur-deficient ore brines and the formation of exhalative base metal deposits     

Fernando Tornos  Christoph A. Heinrich 《Chemical Geology》2008,247(1-2):195-207

The massive sulfide deposits of the Iberian Pyrite Belt are interbedded with felsic volcanic rocks and shale, and underlain by several thousand meters of siliciclastic sedimentary rocks known as the PQ Group. Isotope geochemistry and regional geology are both consistent with equilibration of the ore-forming fluids with the PQ Group, prior to ore deposition near the former seafloor. The average Cu:Zn:Pb ratio of the PQ Group rocks (ca. 26:55:19) is similar to the weighted average of all the massive sulfide orebodies combined (ca. 25:52:23).The genetic relationship between massive sulfide deposits and a siliciclastic sedimentary metal source is explained here by a thermodynamic model, proposing that mildly reducing redox conditions imposed by equilibration with the sedimentary rocks are most critical for the formation of an effective ore-forming fluid. Relatively metal-rich but organic-poor pyrite-bearing shale undergoing dewatering of saline pore fluids is an effective source for the generation of sulfur-deficient but relatively iron and base metal-rich brines. Thus, we propose that the giant deposits of the Iberian Pyrite Belt owe their existence not to exceptionally metal-enriched (e.g., magmatic) fluids, but to the existence of a fairly ordinary but large metal source in reactive siliciclastic sediments, combined with an underlying igneous heat source and a particularly efficient mechanism of sulfide precipitation by mixing with H₂S-rich fluids at or near the seafloor.Essentially similar mineral equilibria are imposed when saline fluids are buffered by typical continental basement rocks. Leaching of retrograde minerals and possibly residual salts from their magmatic or metamorphic prehistory is expected to generate similar, variably metal-rich but relatively sulfide-deficient fluids. Thus, the existence of mildly reducing rocks can be the dominant chemical control in the source of fluids generating many volcanogenic, Irish-type or sedex deposits, many of which are known to precipitate their metal load in response to biogenic sulfide addition at the ore deposition site.  相似文献   

Solar wind helium, neon, and argon isotopic and elemental composition: Data from the metallic glass flown on NASA’s Genesis mission     

Ansgar Grimberg  Heinrich Baur  Peter Bochsler 《Geochimica et cosmochimica acta》2008,72(2):626-645

Solar wind (SW) helium, neon, and argon trapped in a bulk metallic glass (BMG) target flown on NASA’s Genesis mission were analyzed for their bulk composition and depth-dependent distribution. The bulk isotopic and elemental composition for all three elements is in good agreement with the mean values observed in the Apollo Solar Wind Composition (SWC) experiment. Conversely, the He fluence derived from the BMG is up to 30% lower than values reported from other Genesis bulk targets or in-situ measurements during the exposure period. SRIM implantation simulations using a uniform isotopic composition and the observed bulk velocity histogram during exposure reproduces the Ne and Ar isotopic variations with depth within the BMG in a way which is generally consistent with observations. The similarity of the BMG release patterns with the depth-dependent distributions of trapped solar He, Ne, and Ar found in lunar and asteroidal regolith samples shows that also the solar noble gas record of extraterrestrial samples can be explained by mass separation of implanted SW ions with depth. Consequently, we conclude that a second solar noble gas component in lunar samples, referred to as the “SEP” component, is not needed. On the other hand, a small fraction of the total solar gas in the BMG released from shallow depths is markedly enriched in the light isotopes relative to predictions from implantation simulations with a uniform isotopic composition. Contributions from a neutral solar or interstellar component are too small to explain this shallow sited gas. We tentatively attribute this superficially implanted gas to low-speed, current-sheet related SW, which was fractionated in the corona due to inefficient Coulomb drag. This fractionation process could also explain relatively high Ne/Ar elemental ratios in the same initial gas fraction.  相似文献   

Provenance of late Palaeozoic metasediments of the Patagonian proto-Pacific margin (southernmost Chile and Argentina)     

Carita Augustsson  Heinrich Bahlburg 《International Journal of Earth Sciences》2008,97(1):71-88

In this provenance study of late Palaeozoic metasediments of the Eastern Andean Metamorphic Complex (EAMC) along the south Patagonian proto-Pacific margin of Gondwana, the palaeogeological setting of the continental margin in Devonian–Carboniferous and Permian times is reconstructed. The study is based on detrital heavy mineral contents, chemical compositions of tourmaline grains, and whole rock element and Nd-Sr isotopic compositions. Element and isotopic compositions reveal that Devonian–Carboniferous metaturbidites deposited before the development of a Late Carboniferous–Permian magmatic arc along the margin were mainly fed from felsic, recycled, old continental rocks. The last recycling phase involved erosion of metasediments that were exposed in Patagonia. Feeder systems to the basin cut either through epidote-rich or garnet-rich metasediments. In Permian time, EAMC metaturbidites were deposited next to the evolving magmatic arc and were derived from felsic, crustal rocks. Two provenance domains are recognised. The metasediments of the northern one are chemically similar to those of the Devonian–Carboniferous metasediments. This domain was fed from the metasedimentary host rocks of the magmatic arc. The southern domain probably was fed from the arc proper, as indicated mainly by the dominance of metaplutonic lithic fragments, abundant detrital biotite, and the major element composition of the metasediments.  相似文献   

Limits of comprehension, reference frames and general relativity     

Heinrich Eichhorn 《Celestial Mechanics and Dynamical Astronomy》1996,65(1-2):213-222

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Generalized ‘dependencies’ and parameter variance     

Heinrich Eichhorn 《Celestial Mechanics and Dynamical Astronomy》1996,64(3):273-275

The autodependence, (a special case of the — now quite obsolete — dependences, which had been introduced for very specialized astrometric purposes) is proportional to the parameter variance which is the expectation of the variance of the systematic error of a function evaluated with estimated parameters.  相似文献   

Chemical exchange during hydrothermal alteration of basalt by seawater—I. Experimental results for major and minor components of seawater     

Michael J. Mottl  Heinrich D. Holland 《Geochimica et cosmochimica acta》1978,42(8):1103-1115

Fresh mid-ocean ridge basalt of varying crystallinity has been powdered and reacted with seawater and an artificial Na-K-Ca-Cl solution at 200–500°C and 500–1000 bar in sealed gold capsules. Water/rock mass ratios of 1–3 were used and durations ranged from 2 to 20 months.These time periods were sufficient for most elements to approach a steady-state concentration in solution which was determined by equilibrium with alteration minerals (Mg, SiO₂, SO₄), by rate of formation of these minerals (Na, Ca), or by depletion from the rock (K, B, Ba). The resulting solutions closely resemble the brines from the basalt-seawater geothermal system at Reykjanes, Iceland. Mg was almost completely removed from seawater into the alteration products smectite, tremolite-actinolite, or talc. Sulfate also was removed to low concentrations, both by precipitation of anyhydrite and by reduction to sulfide. Net transfer of Na from seawater into solids occurred in most experiments by formation of sodic feldspar and possibly analcime. Sr was removed from seawater in some experiments but showed no change or a small gain in others. SiO₂, Ca, K, Ba, B and CO₂ were leached from basalt and enriched in solution. SiO₂ concentrations were controlled by saturation with quartz at 300°C and above. The principal Ca-bearing phases which formed were anhydrite, the hydrated Ca-silicate truscottite, tremolite-actinolite, and possibly wairakite. No K-rich phases formed. For some minerals the crystallinity of the starting basalt affected the amount which formed.Removal of Mg from seawater into solid alteration products occurred rapidly and was balanced largely by leaching of Ca from basalt. Net transfer of Na from seawater into solids occurred more slowly and was balanced mainly by leaching of additional Ca from basalt. Thus, reaction between seawater and basalt at low water/rock ratios can be considered to consist of two exchanges: Mg for Ca, and Na for Ca.  相似文献