Ultra-Deep Optical Spectroscopy with PMAS. Using the Nod-and-Shuffle Technique

PMAS, the Potsdam Multi-Aperture Spectrophotometer, is a new integral field spectrograph in the optical, which is optimized for good transmission and high image quality from 350 nm to 1 μm. We present our plan to implement a CCD charge-shuffle mode to allow for beam switching with a very high degree of sky subtraction accuracy for faint object 3-D spectroscopy. This revised version was published online in July 2006 with corrections to the Cover Date.     

Rapid Lateglacial tree population dynamics and ecosystem changes in the eastern Baltic region

A growing body of evidence implies that the concept of 'treeless tundra' in eastern and northern Europe fails to explain the rapidity of Lateglacial and postglacial tree population dynamics of the region, yet the knowledge of the geographic locations and shifting of tree populations is fragmentary. Pollen, stomata and plant macrofossil stratigraphies from Lake Kurjanovas in the poorly studied eastern Baltic region provide improved knowledge of ranges of north‐eastern European trees during the Lateglacial and subsequent plant population responses to the abrupt climatic changes of the Lateglacial/Holocene transition. The results prove the Lateglacial presence of tree populations (Betula, Pinus and Picea) in the eastern Baltic region. Particularly relevant is the stomatal and plant macrofossil evidence showing the local presence of reproductive Picea populations during the Younger Dryas stadial at 12 900–11 700 cal. a BP, occurring along with Dryas octopetala and arctic herbs, indicating semi‐open vegetation. The spread of Pinus–Betula forest at ca. 14 400 cal. a BP, the rise of Picea at ca. 12 800 cal. a BP and the re‐establishment of Pinus–Betula forest at ca. 11 700 cal. a BP within a span of centuries further suggest strikingly rapid, climate‐driven ecosystem changes rather than gradual plant succession on a newly deglaciated land. Copyright © 2009 John Wiley & Sons, Ltd.     

The origin of the correlation between the spin parameter and the baryon fraction of galactic disks

The puzzling correlation between the spin parameter λ of galactic disks and the disk-to-halo mass fraction f _disk is investigated. It is shown that such a correlation arises naturally from large uncertainties in determining the virial masses of dark matter halos. This result indicates that halo properties derived from fits to observed rotation curves are still very uncertain. An analysis of λ versus f _disk as function of the adopted halo virial mass shows that for reasonable halo concentrations f _disk ≈ 0.01 - 0.07 which is significantly smaller than the universal baryon fraction. Most of the available gas either never settled into the galactic disks or was ejected subsequently. This revised version was published online in August 2006 with corrections to the Cover Date.     

Late Quaternary vegetation changes around Lake Rutundu,Mount Kenya,East Africa: evidence from grass cuticles,pollen and stable carbon isotopes

Woody, subalpine shrubs and grasses currently surround Lake Rutundu, Mount Kenya. Multiple proxies, including carbon isotopes, pollen and grass cuticles, from a 755‐cm‐long core were used to reconstruct the vegetation over the past 38 300 calendar years. Stable carbon‐isotope ratios of total organic carbon and terrestrial biomarkers from the lake sediments imply that the proportion of terrestrial plants using the C₄ photosynthetic pathway was greater during the Late Pleistocene than in the Holocene. Pollen data show that grasses were a major constituent of the vegetation throughout the Late Pleistocene and Holocene. The proportion of grass pollen relative to the pollen from other plants was greatest at the last glacial maximum (LGM). Grass cuticles confirm evidence that C₄ grass taxa were present at the LGM and that the majority followed the cold‐tolerant NADP‐MEC₄ subpathway. Copyright © 2003 John Wiley & Sons, Ltd.     

Partitioning of Ca and Al between forsterite and silicate melt in dynamic systems with implications for the origin of Ca,Al‐rich forsterites in primitive meteorites

Abstract— We report the results of dynamic crystallization experiments that were specifically designed to study the dependence of Ca and Al partitioning between forsterite and melt in rapidly cooling Caand Al‐rich melts. The partitioning of Ca between olivine and silicate melt is found to be independent of the cooling rate within the range of 1.5 to 1000°C/hr and at CaO contents of up to 25 wt%. Within analytical uncertainty, our data plot on the equilibrium partitioning curve obtained by Libourel (1999). The partitioning behavior of Al at high cooling rates is more complex. Aluminum is much more heterogenously distributed in the olivine and the co‐existing melt than Ca. But, no systematic trend of Al partition coefficient with cooling rate is observed. We apply the results of the experiments to the formation of meteoritic forsterites with relatively high contents of Ca and Al. Although these forsterites are found frequently inside chondrules, the Ca contents of their host chondrules are far too low to crystallize these high Ca‐forsterites. This is also true for very rapid cooling of chondrule melts. The parental melt of these forsterites requires CaO contents above 20 wt%.     

Multiforced statistical assessments of greenhouse-gas-induced surface air temperature change 1890–1985

Based on univariate correlation and coherence analyses and considering the physical basis of the relationships, a simple multiforced (multiple) statistical concept is used which correlates observational climatic time series simultaneously with volcanic, solar, ENSO, and the anthropogenic greenhouse gases forcing. This is appropriate to remove some natural climate noise in the observed data and to evaluate the components (signals) possibly due to the anthropogenic greenhouse gas forcing (CO₂, or equivalent CO₂ implying additional gases) during industrial time. In this paper, we apply this technique to 100 global box data time series 1890–1985, of the surface air temperature, using observed data from Hansen and Lebedeff. The results are presented in terms of latitudinal-seasonal and regional trends, where the observed trend patterns are compared with the hypothetical signals (statistical assessments) possibly due to anthropogenic greenhouse forcing. These latter signals can be amplified to enable a comparison with corresponding results from general circulation model (GCM) CO₂ doubling experiments. These observed-statistical assessments lead to results which are, at least qualitatively and in respect to the zonal mean temperatures, very similar to some GCM experiments indicating the maximum CO₂ doubling signals (statistical assessment > 12 K) in the arctic winter. However, these signals are moderate in the tropics and in the Southern Hemisphere (global average 2.8–4.4 K). As far as the industrial signals are concerned (observed period) these signals are somewhat larger (maximum 7 K, global average 0.5–0.9 K) than the observed trends (maximum 5 K, global average 0.5 K). Phase shifts of cause and effect may amplify these signals but are very uncertain.This paper was presented at the International Conference on Modelling of Global Climate Change and Variability, held in Hamburg 11–15 September 1989 under the auspices of the Meteorological Institute of the University of Hamburg and the Max Planck Institute for Meteorology. Guest Editor for these papers is Dr. L. Dümenil     

Transfer factors of contamination between the German Bight and its tributary waters derived from measured tritium and Cs-137 activity concentrations

Summary Evaluation of the results of radioactivity monitoring in the southern North Sea between 1977 and 1987 has shown that in the water of the German Bight three areas stand out due to their different ratios between salinity and concentration of dissolved Cs-137 and tritium. While salinity steadily increases with greater distance from the coast, the Cs-137 concentration above 34 PSU (Practical Salinity Unit) increases sharply and shows how far water from the western and central North Sea, contaminated by nuclear reprocessing in Sellafield (Irish Sea), reaches into the German Bight. In the 34 to 32.5 PSU range, the influence can be seen of water contaminated by tritium originating in the rivers Rhein, Maas and Schelde, precipitation and the nuclear reprocessing plant at La Hague (Channel). Below 32.5 PSU, the influence of the influx from the rivers Elbe, Weser and Ems becomes apparent. These rivers are less contaminated with tritium.Assuming that Cs-137 and tritium, like the salinity of sea water, behave conservatively and that the decay-time of these two isotopes is long compared with the time-scale of water exchange in the southern North Sea, the concentration values measured are used to calculate the structure of the water masses in the three areas of the German Bight mentioned above using the mixing principle. Evaporation is taken into account. Results show that beyond 34 PSU, about half the sea water originates in the western central North Sea while the other half comes from the Channel. Below 34 PSU, the first mentioned share amounts only to a few per cent. Results also show that fresh water from the Rhein delta and precipitation, increasing with a decrease in salinity from 34 to 32.5 PSU, accounts for a maximum of 5% each. The fresh water influx into the German Bight via the rivers Elbe, Weser and Ems amounts to app. 11% when the PSU value reaches 29. The calculated portions are the mean values for the observation period. The number of measurements available makes it impossible to distinguish more exactly between the temporal and spatial variability of the amounts of the individual components.The quantity of each calculated portion of sea water also represents the transfer factor of concentration between the nuclide concentration in the source (e. g. the Rhein) and the concentration in the German Bight. In addition, these factors are used to calculate the transfer factors of discharge using the annual drainage rates of the sources. Thus a radioactive discharge rate of 10¹⁵ Bq per year into the Rhein would produce a mean activity concentration of 0.34 Bq/l in the German Bight (at a salinity of 33.5 PSU). To verify the calculated transfer factors, tritium concentrations in the German Bight are derived from existing environmental tritium data and the results are compared with the values actually measured.

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Transferkaktoren zwischen der Deutschen Bucht und ihren Zuflüssen abgeleitet aus der Tritium- und Cs-137-Aktivitätskonzentration in den beteiligten Gewässern

Zusammenfassung Eine zusammenhängende Auswertung der Meßergebnisse der Radioaktivitätsüberwachung in der südlichen Nordsee über den Zeitraum 1977 bis 1987 hat gezeigt, daß im Wasser der Deutschen Bucht deutlich drei durch den Salzgehalt des Meerwassers und die Konzentration der gelösten Radionuklide charakterisierte Bereiche zu unterscheiden sind.Während der Salzgehalt mit wachsender Entfernung von der Küste stetig zunimmt, steigt die Cs-137-Konzentration oberhalb 34 PSU (Practical Salinity Unit) sprunghaft an und signalisiert die Grenze, bis zu der das durch die Kernbrennstoff-Wiederaufarbeitung in Sellafield (Irische See) kontaminierte Meerwasser der westlichen und mittleren Nordsee in die Deutsche Bucht vordringt. Im Bereich 34 bis 32,5 PSU ist das von Westen zugeführte, stärker Tritium-kontaminierte Wasser aus Rhein, Maas, Schelde und atmosphärischem Niederschlag zu erkennen, an das sich unterhalb 32,5 PSU der geringer mit Tritum kontaminierte Zufluß aus Elbe, Weser und Ems anschließt.Davon ausgehend, daß sich Cs-137 und Tritium wie der Salzgehalt im Meerwasser konservativ verhalten und daß weiterhin die Halbwertzeit des radioaktiven Zerfalls dieser beiden Nuklide lang ist gegenüber den Wasseraustauschzeiten im betrachteten Meeresgebiet, wurden die in der südlichen Nordsee gemessenen sowie aus der Literatur für den Süßwasserbereich entnommenen Konzentrationswerte dazu genutzt, um rechnerisch mit Hilfe des Mischungsgesetzes den Wassermassenaufbau in den drei genannten Salinitätsbereichen in der Deutschen Bucht quantitativ zu bestimmen. Es zeigte sich, daß oberhalb von 34 PSU das Meerwasser aus etwa gleichen Teilen aus der westlichen/mittleren Nordsee und dem Kanal stammt, während unterhalb dieser Salzgehaltsgrenze nur noch mit wenigen Prozentanteilen Wasser aus der mittleren Nordsee zu finden ist. Ferner ergab sich, daß das aus dem Rheinmündungsbiet bzw, aus dem atmosphärischen Niederschlag stammende Süßwasser — mit sinkendem Salzgehalt steigend — bei 32,5 PSU einen maximalen Anteil von jeweils 5% an Meerwasser hat. Der direkte Süßwasserzufluß aus Elbe, Weser und Ems beträgt in die Deutsche Bucht bei 29 PSU ca. 11%.Die berechneten Anteile sind Mittelwerte über den gesamten Beobachtungszeitraum; die Anzahl der Messungen läßt eine genauere Unterscheidung in zeitliche und räumliche Variabilität der Zusammensetzung nicht zu.Die Größe des jeweils bestimmten Anteils am Meerwasser stellt gleichzeitig den Transferfaktor der Konzentration zwischen der Nuklidkonzentration im Ursprungsgewässer (z. B. dem Rhein) und der sich daraus einstellenden Konzentration in der Deutschen Bucht dar. Ferner wurden die Transferfaktoren der Konzentration in Verbindung mit aus der Literatur entnommenen Größen der jährlichen Abflußmengen der Ursprungsgewässer genutzt, um auch die Transferfaktoren der jährlichen Einbringung zu ermitteln. So ergibt die jährliche Einbringung von 10¹⁵ Bq eines Nuklides z. B. in den Rhein bei 33,5 PSU in der Deutschen Bucht eine mittlere Konzentration von 0,34 Bq/l.Als Anwendungsbeispiel und zur Überprüfung der Richtigkeit der Transferfaktoren wird die Auswertung des Tritiumauslasses bei La Hague auf die Deutsche Bucht berechnet und mit den gemessenen Werten verglichen.

     

The effect of bulk rock composition on the stability of amphibole in the upper mantle: Implications for solidus positions and mantle metasomatism

Summary The stability of pargasitic amphibole in the upper mantle is a function of water content and bulk rock composition, and under water-undersaturated conditions, the stability of amphibole controls the solidus position. Experiments in the system Tinaquillo peridotite +0.2% H₂O, a refractory peridotite under water-undersaturated conditions, show that amphibole is stable to 1030°C and 26 kb. In contrast, pargasitic amphibole is stable to 1150°C and 30 kb in Hawaiian pyrolite, a more fertile peridotite composition. This indicates that under water-undersaturated conditions, the most fertile part of a crystallizing mantle diapir with an inhomogeneous composition will solidify first while a more refractory component will contain an alkali-rich melt which will have the ability to metasomatize adjacent regions. The relative stabilities of amphibole in refractory and fertile bulk compositions may result in increasing rather than diminishing chemical contrasts in high temperature lherzolite, i.e. a process of metamorphic differentiation. Ti, Fe, Al and Na metasomatism can therefore be considered a normal occurrence associated with the upward migration and solidification of an H₂O-bearing mantle diapir.

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Der Einfluß der Gesamtgesteins-Zusammensetzung auf die Stabilität von Amphibol im oberen Mantel: Bedeutung für Solidus-Positionen und Mantel-Metasomatose

Zusammenfassung Die Stabilität pargasitischer Amphibole im oberen Mantel ist eine Funktion von Wassergehalt und Gesamtgesteins-Zusammensetzung. Unter wasser-untersättigten Bedingungen, kontrolliert die Stabilität von Amphibol die Solidus-Position. Experimente in dem System Tinaquillo Peridotit +0,2% H₂O, einem refraktären Peridotit unter wasser-untersättigten Bedingungen, zeigen daß Amphibol bis 1030°C und 26 Kb stabil ist. Im Gegensatz dazu ist pargasitische Hornblende in einem Hawaii-Pyrolit, von mehr fertiler Peridotit-Zuammensetzung, bis 1150°C und 30 Kb stabil. Das zeigt, daß bei wasser-untersättigten Bedingungen der am meisten produktive Teil eines kristallisierenden Mantel-Diapirs mit inhomogener Zusammensetzung sich zuerst verfestigen wird, während eine mehr refraktäre Komponente eine alkali-reiche Schmelze enthalten wird, die wiederum die Fähigkeit hat, umliegende Bereiche metasomatisch zu beeinflussen. Die relativen Stabilitäten von Amphibol in refraktären und fertilen Gesamtzusammensetzungen können dazu führen, daß die chemischen Gegensätze in Hochtemperaturlherzoliten eher zunehmen als abnehmen, d. h. ein Prozeß metamorpher Differentiation. Ti, Fe, Al und Na Metasomatose können deshalb als ein verbreiteter Vorgang, der mit der Aufwärtsbewegung und Verfestigung eines H₂O-führenden Mantel-Diapirs assoziiert ist, betrachtet werden.

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With 4 Figures     

New compositional and optical data for antimonian and bismuthian varieties of hemusite from Japan

Summary New compositional and optical data are reported for antimonian and antimonianbismuthian varieties of hemusite from epithermal Au-Ag-Cu deposits in Japan. The empirical formula for the antimonian variety, from the Iriki mine is: (Cu_5.83Fe_0.14Ag_0.01)_5.98Mo_1.03(Sn_0.54Sb_0.41Te_0.03Bi_0.02)_1.00(S_7.85Se_0.15)_8.00, and that of the Sb-Bi variety from the Kawazu mine is: (Cu_5.84Fe_0.14Ag_0.01)_5.99Mo_1.03(Sn_0.82Sb_0.11Bi_0.l0Te_0.04)_1.07(S_7.80Se_0.12)_7.92. The theoretical formula of hemusite is Cu⁺ ₄Cu²⁺ ₂MO⁴⁺Sn⁴⁺S₈, whilst the most probable formula of the Iriki hemusite is Cu⁺ _4.5CU²⁺ _1.5Mo⁴⁺Sn⁴⁺ _0.5Sb⁵⁺ _0.5S₈, with Sb⁵⁺ substituting for Sn⁴⁺ and forming (SbS₄)^3– tetrahedra as might be expected, given that the metal to sulphur ratio is 1, and given the sphalerite-like structure of the mineral. However Bi³⁺ cannot be so accommodated, resulting in a deficiency in (S + Se) for Kawazu hemusite. Reflectance spectra for both are compared with those of the tungsten analogue (compositional) of hemusite, kiddcreekite. The relationship between hemusitesensu stricto and these newly reported varieties is discussed in terms of simple and coupled chemical substitutions, and inferences are drawn on the valency of Sb, Bi, Mo and Cu in the hemusite structure.

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Neue chemische und optische Daten für antimon- und bismuthführende Varietäten von Hemusit aus Japan

Zusammenfassung Neue chemische und optische Daten für antimon- und bismuthführende Hemusite auf epithermalen Au-Ag-Cu Lagerstätten in Japan werden vorgelegt. Die empirische Formel für die antimon-führende Varietät aus der Iriki-Mine ist: (Cu_5.83Fe_0.14Ag_0.01)_5.98Mo_1.03(Sn_0.54Sb_0.41Te_0.03Bi_0.02)_1.00 (S_7.85Se_0.15)_8.00, und die der Sb-Bi Varietät aus der Kawazu Mine ist: (Cu_5.84Fe_0.14Ag_0.01)_5.99M0_1.03(Sn_0.82Sb_0.11Bi_0.l0Te_0.04)_1.07 (S_7.80Se_0.12)_7.92. Die theoretische Formel von Hemusit ist Cu⁺ ₄Cu²⁺ ₂Mo⁴⁺Sn⁴⁺S₈, während die wahrscheinlichere Formel für den Hemusit von Iriki Cu⁺ ₄Cu²⁺ _1.5Mo⁴⁺Sn⁴⁺ _0.5Sb⁵⁺ _0.5S₈, mit Sb⁵⁺ an der Stelle von Sn⁴⁺, das(SbS₄)^3– Tetraeder bildet, wie zu erwarten ist, unter der Voraussetzung, da das Metall zu Schwefelverhältnis 1 und die Struktur sphaleritähnlich ist. Bi³⁺ kann jedoch nicht in dieser Weise untergebracht werden, und das führt zu einem Mangel an (S + Se) für den Hemusit von Kawazu. Die Reflektions-Spektren beider Minerale werden mit denen des Wolfram-Equivalents von Hemusit (Kiddcreekit) verglichen. Die Beziehung zwischen Hemusitsensu stricto und diesen jetzt beschriebenen Varietäten wird auf der Basis einfacher und gekoppelter chemischer Substitution diskutiert. Auf dieser Basis werden Schlüsse auf die Valenz von Sb, Bi Mo und Cu in der Hemusit-Struktur gezogen.