On the possibility of earth-type habitable planets around 47 UMa

We investigate whether Earth-type habitable planets can in principle exist in the planetary system of 47 UMa. The system of 47 UMa consists of two Jupiter-size planets beyond the outer edge of the stellar habitable zone, and thus resembles our own Solar System most closely compared to all exosolar planetary systems discovered so far. Our study of habitability deliberately follows an Earth-based view according to the concept of Franck and colleagues, which assumes the long-term possibility of photosynthetic biomass production under geodynamic conditions. Consequently, a broad variety of climatological, biogeochemical, and geodynamical processes involved in the generation of photosynthesis-driven life conditions is taken into account. The stellar luminosity and the age of the star/planet system are of fundamental importance for planetary habitability. Our study considers different types of planetary continental growth models and takes into account a careful assessment of the stellar parameters. In the event of successful formation and orbital stability, two subjects of intense research, we find that Earth-type habitable planets around 47 UMa are in principle possible! The likelihood of those planets is increased if assumed that 47 UMa is relatively young (?6 Gyr) and has a relatively small stellar luminosity as permitted by the observational range of those parameters.     

A simple model for lensing by black holes in galactic nuclei

The lensing properties of the Plummer model with a central point mass and external shear are derived, including the image multiplicities, critical curves and caustics. This provides a simple model for a flattened galaxy with a central supermassive black hole. For the Plummer model with black hole, the maximum number of images is four, provided the black hole mass is less than an upper bound which is calculated analytically. This introduces a method to constrain black hole masses by counting images, thus applicable at cosmological distance. With shear, the maximum number of images is six and we illustrate the occurrence of an astroid caustic and two metamorphoses.     

The global Frasnian-Famennian »Kellwasser Event«

During the UppermostP. gigas conodont zone (P. linguiformis zone) the stepwise Frasnian extinction culminates in the global transgressive-regressive Frasnian-Famennian »Kellwasser event«. Most pelagic organisms of the tropical marine environment are more or less affected by this mass extinction. During the early Upper Devonian extinction rates are clearly related to the deposition of black shales and the storage of a great amount of organic carbon in the (shelf) sediments. Contemporaneous positive excursions of the ¹³C recorded from pelagic limestones of Europe and Australia prove a worldwide change in the CO₂ content of the oceans surface water which is in balance with the atmosphere. If the climate is controlled by the CO₂ content of the atmosphere, a cyclic operation process might have developed with the succession: transgression — high organic production — deposition of organic carbon — lowering of CO₂ in the atmosphere — icehouse effect — polar glaciation — regression — erosion of organic carbon and re-supply of CO₂ to the ocean and atmosphere — greenhouse effect — deglaciation — transgression. During the change from a greenhouse to an icehouse effect an overturn of the anoxic oceans probably was one of the causes for the mass killing of low latitude marine organisms.

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Zusammenfassung Während der OberstenP. gigas-Zone (=P. linguiformis-Zone) kulminiert das stufenweise Erlöschen der Frasne Organismen im globalen transgressiv-regressiven »Kellwasser-Ereignis«, das die Frasne-Famenne-Grenze markiert. Die meisten Organismengruppen der tropischen Meere werden mehr oder weniger von dem Massensterben betroffen. Während des tiefen Oberdevons sind die Aussterberaten offensichtlich mit der Ablagerung von Schwarzschiefern verknüpft, in denen eine große Menge organischen Kohlenstoffs auf den Schelfen fixiert wird. Gleichzeitige positive Exkursionen der ¹³C-Kurven, die in pelagischen Kalken aus Europa und Australien gemessen wurden, deuten auf eine weltweite Änderung der CO₂-Gehalte des ozeanischen Oberflächenwassers und der Atmosphäre hin.Sollte das Klima vom CO₂ in der Atmosphäre gesteuert werden, könnte sich folgender Autozyklus entwickelt haben: Transgression — hohe organische Produktion — Ablagerung von organischem Kohlenstoff — Erniedrigung des CO₂-Gehaltes in der Atmosphäre — Abkühlung — polare Vereisung-Regression — Erosion und Oxidation von organischem Kohlenstoff — Erhöhung des CO₂-Gehaltes in der Atmosphäre — Treibhauseffekt — Abschmelzen der polaren Vereisung — Transgression. Aufsteigende anoxische Wässer beim Übergang vom Treibhaus- zum »Kühlhauseffekt« dürften eine der Ursachen für das Massensterben tropischer mariner Organismen gewesen sein.

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Résumé Au cours de la partie supérieure de la zone de conodontes àP. gigas (= zone àP. linguiformis), l'extinction progressive des organismes frasniens a culminé au moment de l'événement de Kellwasser, marqué par une transgression-régression globale à la limite Frasnien-Famennien. La plupart des organismes pélagiques des milieux marins tropicaux ont été affectés à des degrés divers par cette extinction de masse. Pendant le début du Dévonien supérieur, les taux d'extinction sont clairement en relation avec le dépôt de boues noires et le stockage d'une grande quantité de matière organique dans les sédiments de shelf. Simultanément, des variations positives de ¹³C enregistrées dans des calcaires pélagiques d'Europe et d'Australie indiquent un changement modial de la teneur en CO₂ de l'eau de surface des océans et de l'atmosphère.Si on admet que le climat est régi par la teneur en CO₂ de l'atmosphère, le processus cyclique suivant a pu se développer: transgression — forte production organique — dépôt de carbone organique — baisse de la teneur en CO₂ de l'atmosphère — refroidissement — glaciation polaire — régression — érosion et oxydation du carbone organique — élévation de la teneur en CO₂ de l'atmosphère — effet de serre — fusion des glaces polaires — transgression. Lors du passage du stade de l'effet de serre à celui du refroidissement, une remontée des eaux anoxiques océaniques peut être à l'origine de l'extinction de masse des organismes marins tropicaux.

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Determination of fluid/melt partition coefficients by LA-ICPMS analysis of co-existing fluid and silicate melt inclusions: Controls on element partitioning

Analyses of co-existing silicate melt and fluid inclusions, entrapped in quartz crystals in volatile saturated magmatic systems, allowed direct quantitative determination of fluid/melt partition coefficients. Investigations of various granitic systems (peralkaline to peraluminous in composition, log fO₂ = NNO−1.7 to NNO+4.5) exsolving fluids with various chlorinities (1-14 mol/kg) allowed us to assess the effect of these variables on the fluid/melt partition coefficients (D). Partition coefficients for Pb, Zn, Ag and Fe show a nearly linear increase with the chlorinity of these fluid (D_Pb ∼ 6 ∗ m_Cl, D_Zn ∼ 8 ∗ m_Cl, D_Ag ∼ 4 ∗ m_Cl, D_Fe ∼ 1.4 ∗ m_Cl, where m_Cl is the molinity of Cl). This suggests that these metals are dissolved primarily as Cl-complexes and neither oxygen fugacity nor the composition of the melt affects significantly their fluid/melt partitioning. By contrast, partition coefficients for Mo, B, As, Sb and Bi are highest in low salinity (1-2 mol/kg Cl) fluids with maximum values of D_Mo ∼ 20, D_B ∼ 15, D_As ∼ 13, D_Sb ∼ 8, D_Bi ∼ 15 indicating dissolution as non-chloride (e.g., hydroxy) complexes. Fluid/melt partition coefficients of copper are highly variable, but highest between vapor like fluids and silicate melt (D_Cu ? 2700), indicating an important role for ligands other than Cl. Partition coefficients for W generally increase with increasing chlorinity, but are exceptionally low in some of the studied brines which may indicate an effect of other parameters. Fluid/melt partition coefficients of Sn show a high variability but likely increase with the chlorinity of the fluid (D_Sn = 0.3-42, D_W = 0.8-60), and decrease with decreasing oxygen fugacity or melt peraluminosity.     

Calcium isotope (δCa) fractionation along hydrothermal pathways, Logatchev field (Mid-Atlantic Ridge, 14°45′N)

We investigate the Logatchev Hydrothermal Field at the Mid-Atlantic Ridge, 14°45′N to constrain the calcium isotope hydrothermal flux into the ocean. During the transformation of seawater to a hydrothermal solution, the Ca concentration of pristine seawater ([Ca]_SW) increases from about 10 mM to about 32 mM in the hydrothermal fluid endmember ([Ca]_HydEnd) and thereby adopts a δ^44/40Ca_HydEnd of −0.95 ± 0.07‰ relative to seawater (SW) and a ⁸⁷Sr/⁸⁶Sr isotope ratio of 0.7034(4). We demonstrate that δ^44/40Ca_HydEnd is higher than that of the bedrock at the Logatchev field. From mass balance calculations, we deduce a δ^44/40Ca of −1.17 ± 0.04‰ (SW) for the host-rocks in the reaction zone and −1.45 ± 0.05‰ (SW) for the isotopic composition of the entire hydrothermal cell of the Logatchev field. The values are isotopically lighter than the currently assumed δ^44/40Ca for Bulk Earth of −0.92 ± 0.18‰ (SW) [Skulan J., DePaolo D. J. and Owens T. L. (1997) Biological control of calcium isotopic abundances in the global calcium cycle. Geochim. Cosmochim. Acta61,(12) 2505-2510] and challenge previous assumptions of no Ca isotope fractionation between hydrothermal fluid and the oceanic crust [Zhu P. and Macdougall J. D. (1998) Calcium isotopes in the marine environment and the oceanic calcium cycle. Geochim. Cosmochim. Acta62,(10) 1691-1698; Schmitt A. -D., Chabeaux F. and Stille P. (2003) The calcium riverine and hydrothermal isotopic fluxes and the oceanic calcium mass balance. Earth Planet. Sci. Lett. 6731, 1-16]. Here we propose that Ca isotope fractionation along the fluid flow pathway of the Logatchev field occurs during the precipitation of anhydrite. Two anhydrite samples from the Logatchev Hydrothermal Field show an average fractionation of about Δ^44/40Ca = −0.5‰ relative to their assumed parental solutions. Ca isotope ratios in aragonites from carbonate veins from ODP drill cores indicate aragonite precipitation directly from seawater at low temperatures with an average δ^44/40Ca of −1.54 ± 0.08‰ (SW). The relatively large fractionation between the aragonite precipitates and seawater in combination with their frequent abundance in weathered mafic and ultramafic rocks suggest a reconsideration of the marine Ca isotope budget, in particular with regard to ocean crust alteration.     

Phytoreduction and volatilization of mercury by ascorbate in Arabidopsis thaliana, European beech and Norway spruce

Mercury vapor (Hg⁰) emission from plants contributes to the atmospheric Hg cycle. Young barley (Hordeum vulgare L.) plants grown on a hydroponic cultivation medium containing Hg(II) have previously been shown to increase their Hg⁰ emission significantly by reduction of Hg(II) with endogenous ascorbic acid. Regarding the potential contribution to the Hg cycle from the vast forest-covered areas, it was important to investigate this mechanism in trees. The increase in Hg⁰ emission from young European beech plants cultivated on a HgCl₂ medium exceeded that from controls by ca. tenfold and was proportional to the Hg(II) concentration. From these experiments, a flux of 12.8 μg Hg⁰/h/m² was estimated at an exposure of the roots to 20 μM Hg(II). Mercury vapor release from homogenates of Norway spruce needles exceeded that from European beech leaves by a factor of 2.3–4, i.e. in proportion to the reported AA concentrations; the reduction was maximal at alkaline pH which is typical for AA. The 8.4-fold difference in Hg⁰ release between homogenates from wild-type Arabidopsis thaliana and from its AA-deficient mutant vtc 1-1 also paralleled the reported difference in AA levels of both species. It is concluded that the phytoreduction and vaporization of Hg by AA is an important mechanism as much for Hg detoxification in trees as for Hg emission to the atmosphere. The efficiency of this process seems to result from the optimal coordination of transfer and biochemical transformation of mercuric ions and Hg vapor. There is no evidence for a relevant difference in the mechanisms of biogenic Hg(II) reduction between grass plants and trees.     

Trace element diagenesis in pyrite-rich sediments of the Achterwasser lagoon, SW Baltic Sea

The early diagenesis of trace elements (V, Cr, Co, Cu, Zn, As, Cd, Ba, U) in anoxic sediments of the Achterwasser, a shallow lagoon in the non-tidal Oder estuary in the Baltic Sea, was investigated in the context of pyrite formation. The dissolved major redox parameters show a two-tier distribution with transient signals in the occasionally re-suspended fluid mud layer (FM) and a permanently established diagenetic sequence in the sediment below. Intense microbial respiration leads to rapid depletion of O₂ within the uppermost mm of the FM. The reduction zones of Mn, Fe and sulfate overlap in the FM and in the permanently anoxic sediment section which appears to be a typical feature of estuarine sediments, under low-sulfate conditions. Degrees of pyritization (DOP) range from 50% in the FM to remarkably high values > 90% at 50 cm depth. Pyrite formation at the sediment surface is attributed to the reaction of Fe-monosulfides with intermediate sulfur species via the polysulfide pathway. By contrast, intense pyritization in the permanently anoxic sediment below is attributed to mineral growth via adsorption of aqueous Fe-sulfide complexes onto pyrite crystals which had originally formed in the surface layer.The studied trace elements show differential behavior patterns which are closely coupled to the diagenetic processes described above: (i) Zn, Cu and Cd are liberated from organic matter in the thin oxic layer of the sediment and diffuse both upwards across the sediment/water boundary and downwards to be trapped as monosulfides, (ii) V, Cr, Co and As are released during reductive dissolution of Mn- and Fe-oxyhydroxides, (iii) U removal from pore water occurs concomitantly to Fe reduction in the FM and is attributed to reduction of U(VI) to U(IV), (iv) the Ba distribution is controlled by reductive dissolution of authigenic barite in the sulfate reduction zone coupled with upward diffusion and re-precipitation. The incorporation of trace elements into pyrite is most intense for Co, Mn and As, intermediate for Cu and Cr and little to negligible for U, Zn, Cd, V and Ba. The observed trend is largely in agreement with previous studies and may be explained with differing rates for ligand exchange. Slow and fast ligand exchange and thus precipitation kinetics are also displayed by downcore increasing (Mn, Cr, Co and As) or constantly low (Zn, Cu, Cd) pore water concentrations. The downward increasing degrees of trace metal pyritization (DTMP) for Co, Cu, Zn and As are, in analogy to pyrite growth, assigned to adsorption of sulfide complexes or As oxyanions onto preexisting pyrite minerals.     

Environmental overview of Eckernförde Bay,northern Germany

This environmental overview of Eckernförde Bay (northern Germany) summarizes the results of previous studies relevant to the Office of Naval Research's Coastal Benthic Boundary Layer (CBBL) Baltic field exercise conducted during 1993–1994. Significant environmental characteristics include the following: (1) surface sediment distribution is related to water depth, dictated primarily by hydrodynamic reworking of older glacial deposits; (2) the origin and characteristics of small-scale sedimentary structures depend on storm-generated waves and currents; (3) the proximity of the sea surface and sediment —water interface results in a pelagic—benthic coupling that drives biogeochemical processes and produces organicrich, acoustically turbid sediments; and (4) the bay floor is complicated topographically by pockmarks and manmade sedimentary structures.     

The influence of salinity on the heat-shock protein response of Potamocorbula amurensis (Bivalvia)

For biomarkers to be useful in assessing anthropogenic impacts in field studies involving aquatic organisms, they should not be affected by naturally occurring changes in environmental parameters such as salinity. This is especially important in estuarine environments and for relatively unspecific biomarkers like heat-shock proteins (hsps, stress proteins). In this study, the heat-shock protein response was measured in the euryhaline clam, Potamocorbula amurensis, after exposure to a range of salinities reflecting normal and extreme environmental conditions in Northern San Francisco Bay, California. The ability to raise cellular hsp70 levels in response to heat-shock was significantly impaired in P. amurensis collected from a low (0.5 ppt) salinity field site, and after 14 day exposure to low salinity in the laboratory.