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71.
Kurt Lambeck 《Celestial Mechanics and Dynamical Astronomy》1974,10(2):179-182
Douglaset al. (1973) have estimated tidal parameters from the orbits of GEOS 1 and GEOS 2. Their results, interpreted in terms of Love numbers, are rather dispersive due in part to their neglect of the ocean tides. The ocean tidal corrections are estimated in this paper, but although they do not explain all of the discrepancy they do emphasise the importance of these perturbations on the motion of close Earth satellites. The remaining discrepancies could result in part from the fact that part of the long period tidal perturbations have been absorbed by the zonal harmonics in the Earth's gravity field. 相似文献
72.
The mixing behaviour of iron, manganese, phosphate and humic acid in a Delaware salt marsh creek was studied using field data, laboratory mixing experiments, and geochemical mass balance equations. Property-salinity diagrams for field data indicated that the removal of iron is 56–70% in the 0–10‰ salinity range. A proposed mechanism of removal is the flocculation of colloidal iron, perhaps with humic acid. Phosphate, however, undergoes 195% addition in the same low salinity region, which may be due to release of phosphate from resuspended sediments. Dissolved manganese is conserved, as is humic acid throughout the salt marsh mixing zone. Within the uncertainty of the data the maximum possible removal of humic acid is 23%.Laboratory mixing experiments that simulated salt marsh mixing along the same salinity gradient as observed in the field (5–25‰) showed only small-scale additions and removals compared to the field results. Such small-scale changes occurred largely at salinities >10‰ in the laboratory experiments, whereas most removals and additions occurred at salinities <10‰ in the field. Mixing studies also showed little difference between prefiltered and unfiltered mixes. The studies suggest that simple mixing of salt marsh waters, with or without suspended material, does not strongly influence the observed behaviour of dissolved constituents in salt marshes, and that other processes (e.g. sediment or intertidal exchange) must dominate their behaviour. 相似文献
73.
The Valhalla uranium deposit, located 40 km north of Mount Isa, Queensland, Australia, is an albitite-hosted, Mesoproterozoic
U deposit similar to albitite-hosted uranium deposits in the Ukraine, Sweden, Brazil and Guyana. Uranium mineralisation is
hosted by a thick package of interbedded fine-grained sandstones, arkoses and gritty siltstones that are bound by metabasalts
belonging to the ca. 1,780 Ma Eastern Creek Volcanics in the Western Succession of the Mount Isa basin. Alteration associated
with U mineralisation can be divided into an early, main and late stage. The early stage is dominated by laminated and intensely
altered rock comprising albite, reibeckite, calcite, (titano)magnetite ± brannerite. The main stage of mineralisation is dominated
by brecciated and intensely altered rocks that comprise laminated and intensely altered rock cemented by brannerite, apatite,
(uranoan)-zircon, uraninite, anatase, albite, reibeckite, calcite and hematite. The late stage of mineralisation comprises
uraninite, red hematite, dolomite, calcite, chlorite, quartz and Pb-, Fe-, Cu-sulfides. Brannerite has U–Pb and Pb–Pb ages
that indicate formation between 1,555 and 1,510 Ma, with significant Pb loss evident at ca. 1,200 Ma, coincident with the
assemblage of Rodinia. The oldest ages of the brannerite overlap with 40Ar/39Ar ages of 1,533 ± 9 Ma and 1,551 ± 7 Ma from early and main-stage reibeckite and are interpreted to represent the timing
of formation of the deposit. These ages coincide with the timing of peak metamorphism in the Mount Isa area during the Isan
Orogeny. Lithogeochemical assessment of whole rock data that includes mineralised and unmineralised samples from the greater
Mount Isa district reveals that mineralisation involved the removal of K, Ba and Si and the addition of Na, Ca, U, V, Zr,
P, Sr, F and Y. U/Th ratios indicate that the ore-forming fluid was oxidised, whereas the crystal chemistry of apatite and
reibeckite within the ore zone suggests that F− and were important ore-transporting complexes. δ18O values of co-existing calcite and reibeckite indicate that mineralisation occurred between 340 and 380°C and involved a
fluid having δ18Ofluid values between 6.5 and 8.6‰. Reibeckite δD values reveal that the ore fluid had a δDfluid value between −98 and −54‰. The mineral assemblages associated with early and main stages of alteration, plus δ18Ofluid and δDfluid values, and timing of the U mineralisation are all very similar to those associated with Na–Ca alteration in the Eastern
Succession of the Mount Isa basin, where a magmatic fluid is favoured for this style of alteration. However, isotopic data
from Valhalla is also consistent with that from the nearby Mount Isa Cu deposit where a basinal brine is proposed for the
transport of metals to the deposit. Based on the evidence to hand, the source fluids could have been derived from either or
both the metasediments that underlie the Eastern Creek Volcanics or magmatism that is manifest in the Mount Isa area as small
pegmatite dykes that intruded during the Isan Orogeny. 相似文献
74.
Kurt Kalle 《Ocean Dynamics》1951,4(3):92-96
Zusammenfassung Die bisherigen Methoden zur Bestimmung des Chlorophylls im Meerwasser benötigen zu ihrer Durchführung Wassermengen von einem bis zu einigen Litern. Sie sind infolgedessen zur Ausfühung serienmäßiger ozeanischer Messungen noch nicht voll geeignet. Durch Ausnutzung der intensiven Rotfluoreszenz des Chlorophylls und Benutzung kleinerer und engerer Kolorimeterröhren läßt es sich ermöglichen, den Wasserbedarf bis auf 100 ccm und weniger je Probe herabzudrücken und somit diesen Mangel zu beheben. Die für diesen Zweck geschaffene gleiche Arbeitsapparatur ermöglicht weiterhin, im Anschluß an die Chlorophyllbestimmung ohne wesentlich erhöhte Arbeitsbelastung die Bestimmung der Eigenfluoreszenz gleichfalls auf dem Wege der Mikromethodik an nur 1 ccm Meerwasser durchzuführen.
Die sechs vorhergehenden Mitteilungen sind in den Annalen der Hydrographie und maritimen Meteorologie erschienen, und zwar I:59, 1931, 313; II:61, 1933, 124; III:62, 1934, 65; IV:63, 1935, 58: V:63, 1935, 195; VI:65, 1937, 276. 相似文献
Investigations in chemical oceanography carried out with the aid of the Pulfrich photometer
Summary The old method of determining the chlorophyll content of sea water required a comparatively great quantity of sea water (one or severel litres) and, hence, was not suitable in case of serial measurements. The utilization of the intensive red fluorescence of chlorophyll and the use of small and narrow colorimeter tubes render it possible to minimize the required quantity of water to 100 ccm and less per sample. The apparatus which was especially constructed for this purpose being fit for the determination of both the chlorophyll content and the proper fluorescence, the latter can be easily determined immediately after the determination of the chlorophyll content by means of the micro-method from only 1 ccm of sea water.
Investigations chimiques dans le domaine océanographique à l'aide du photomètre de PulfrichVIIe communication. Les micro déterminations de la teneur en chlorophylle et de la fluorescence propre de l'eau de mer
Résumé La quantité minimale nécessaire pour déterminer la teneur en chlorophylle selon la méthode en usage jusqu' à présent se montait d'un à plusieurs litres; à cause de cela cette méthode n'était pas convenable pour des mensurations en séries. En se servant de l'intensive fluorescence rouge de la chlorophylle et en employant un petit tube étroit à colorimètre il est possible de limiter la quantité d'eau à 100 ccm et moins par échantillon. En outre, on peut se servir du même appareil pour déterminer la fluorescence propre selon la nouvelle méthode. Pour cette détermination qui peut être effectué sans peine immédiatement après celle de la chlorophylle on a besoin de seulement 1 ccm d'eau de mer.
Die sechs vorhergehenden Mitteilungen sind in den Annalen der Hydrographie und maritimen Meteorologie erschienen, und zwar I:59, 1931, 313; II:61, 1933, 124; III:62, 1934, 65; IV:63, 1935, 58: V:63, 1935, 195; VI:65, 1937, 276. 相似文献
75.
Graph theory is useful for analyzing time-dependent model parameters estimated from interferometric synthetic aperture radar (InSAR) data in the temporal domain. Plotting acquisition dates (epochs) as vertices and pair-wise interferometric combinations as edges defines an incidence graph. The edge-vertex incidence matrix and the normalized edge Laplacian matrix are factors in the covariance matrix for the pair-wise data. Using empirical measures of residual scatter in the pair-wise observations, we estimate the relative variance at each epoch by inverting the covariance of the pair-wise data. We evaluate the rank deficiency of the corresponding least-squares problem via the edge-vertex incidence matrix. We implement our method in a MATLAB software package called GraphTreeTA available on GitHub (https://github.com/feigl/gipht). We apply temporal adjustment to the data set described in Lu et al. (Geophys Res Solid Earth 110, 2005) at Okmok volcano, Alaska, which erupted most recently in 1997 and 2008. The data set contains 44 differential volumetric changes and uncertainties estimated from interferograms between 1997 and 2004. Estimates show that approximately half of the magma volume lost during the 1997 eruption was recovered by the summer of 2003. Between June 2002 and September 2003, the estimated rate of volumetric increase is \((6.2 \, \pm \, 0.6) \times 10^6~\mathrm{m}^3/\mathrm{year} \). Our preferred model provides a reasonable fit that is compatible with viscoelastic relaxation in the five years following the 1997 eruption. Although we demonstrate the approach using volumetric rates of change, our formulation in terms of incidence graphs applies to any quantity derived from pair-wise differences, such as range change, range gradient, or atmospheric delay. 相似文献
76.
Kurt v. Gehlen A. Maucher G. Müller G. C. Amstutz H. J. Koark 《Mineralium Deposita》1972,7(1):106-110
77.
78.
Prof. Dr. Kurt Wegener 《Pure and Applied Geophysics》1951,19(3-4):170-172
Zusammenfassung Die Solarkonstante 2.4 wird begründet.
Summary The true solar constant 2.4 is proved.相似文献
79.
Prof. Dr. Kurt Wegener 《Pure and Applied Geophysics》1951,20(1):85-85
Ohne Zusammenfassung 相似文献
80.
Kurt Kalle 《Ocean Dynamics》1949,2(4):117-124
Zusammenfassung In der folgenden Arbeit wird der erstmalige Versuch unternommen, einen quantitativen Einblick in die gegenseitigen Beziehungen zweier im Meerwasser vorhandenen ausgesprochen organischen Stoffe in ihrer Abhängigkeit vom Salzgehalt zu gewinnen. Derartige Messungen waren bisher noch nicht möglich vor allem wegen der überaus geringen Konzentration, in der die organischen Stoffe im Meerwasser vorzukommen pflegen, sodann auch wegen der verhältnismäßig großen Abbaugeschwindigkeit, der diese Stoffe unter den natürlichen Bedingungen im Meere unterliegen. Bei den hier angestellten Untersuchungen handelt es sich um zwei verhältnismäßig stabile den Humusstoffen nahestehende Verbindungen, die sich einmal durch ihr Vermögen, im ultravioletten Licht zu fluoreszieren und zum anderen durch ihre gelbe Farbe auszeichnen. Als Untersuchungsgebiet wurden der Bottnische und Finnische Meerbusen ausgewählt, die an diesen Stoffen verhältnismäßig reich sind. Legt man vier Ausgangswässer zugrunde, so läßt sich die eigenartige Verteilung dieses Fluoreszenz- und Gelb-Stoffes in dem Untersuchungsgebiet zwangslos aus den gegenseitigen Mischungsvorgängen dieser Wässer deuten. Der Vorzug der neuartigen Methodik für zukünftige Messungen liegt in dreierlei. Erstens verspricht die Bestimmung eine tieferen Einblick in den bisher noch so ungeklärten Mechanismus der Humusbildung, ferner ermöglicht sie eine genauere Kontrolle des Aussüßungsvorganges in den Randmeergebieten als es bisher möglich war, und schließlich scheint sie berufen, bei weiterer Durchentwicklung der Methodik für die Aufklärung der chemisch-biologischen Grundvorgänge im Zusammenhang mit der Produktionsfrage des Meeres eine wichtige Lücke ausfüllen zu können.
Die Veröffentlichung der im wesentlichen bereits vor etwa zehn Jahren abgeschlossenen Arbeit ist durch den Krieg verzögert worden. 相似文献
Fluorescence and contents of yellow substance in the Gulfs of Bothnia and Finland
Summary In the following paper it is tried for the first time to provide a quantitative insight into the relations between two clearly organic substances in the sea-water as depending on salinity. Measurings of this kind could not be made so far especially because the organic substances usually occur in sea-water in very low concentration, furthermore because they decay rather rapidly under the natural conditions prevailing in the sea. The investigations in question deal with two relatively stable compositions closely related to the ulmous substances which are characterized on the one hand by their capability of fluorescence in ultraviolet light and on the other hand by their yellow colour. The investigations are based on water-samples from the Gulfs of Bothnia and Finland, which are relatively abounding in these substances. Assuming four primary kinds of water, the peculiar distribution of these fluorescence and yellow substances in the investigated area can be explained without restriction by mixing processes of these waters. The advantages of the new method of investigation are: firstly that it may be expected to get a deeper insight into the genesis of humus which is only very little elucidated so far, furthermore it allows to control more exactly the process of freshening of the water in marginal seas, and finally, in case of further development it seems to be qualified to fill up a remarkable gap in the elucidation of the fundamental processes in biological chemistry in connection with the problem of marine production.
Die Veröffentlichung der im wesentlichen bereits vor etwa zehn Jahren abgeschlossenen Arbeit ist durch den Krieg verzögert worden. 相似文献