Microbial Degradation of Tar Oil Compounds under Different Redox Conditions

The microbial transformation of typical tar oil compounds such as acridine, benzo(b)thiophene, dibenzofuran, indane, and indene under different redox conditions was investigated in microcosm studies. Under aerobic conditions the inherent contamination in polluted soil as well as the added N‐, S‐, O‐ heterocyclic and homocyclic compounds were transformed predominantly apart from thiophene. 1‐Indanone was detected by RP‐HPLC‐DAD and GC‐MS as an intermediate metabolite from indane and indene. Under nitrate and sulfate reducing conditions indane, benzo(b)thiophene, and dibenzofuran were transformed in assays with the polluted soil samples from well B 65 and B 66 within 426 days, whereas they were persistent in assays with the highly polluted soil B 67. All heterocyclic and homocyclic compounds added to the non‐contaminated soil from well B 85 were not degraded under nitrate and sulfate reducing conditions, too. The results indicate that for the decision, wether natural attenuation can be implemented in the remediation of contaminated site, in addition to BTEX and PAHs especially the fate of further tar oil compounds in anoxic aquifers has to be considered.     

Über stratigraphische Untersuchungsmethoden in rezenten Tiefseesedimenten

Zusammenfassung Durch Bestimmung der Foraminiferenanzahl in I g Sediment wird die biostratigraphische Untersuchungsmethode, die mittels einer qualitativen und quantitativen Erfassung der Foraminiferenfauna in den Tiefseekernen der deutschen Meteor-Expedition und schwedischen Albatroß-Expedition durchgeführt werden ist, auf ihre Richtigkeit hin geprüft. Die Untersuchung hat die Anwendbarkeit dieser stratigraphischen Methode bestätigt. Sie hat daneben wiederum gezeigt, daß die Verbreitung und Entwicklung der einzelnen Foraminiferenarten vor allem von der Temperatur des Meerwassers abhängig sind; andere Faktoren wie Phosphatgehalt des Wassers usw. scheinen in dieser Hinsicht eine mehr untergeordnete Rolle zu spielen. Unter gewissen Voraussetzungen können Tiefseekerne durch Bestimmung der Foraminiferenanzahl je 1 g Sediment in groben Zügen stratigraphisch gegliedert werden; auch kann die Individuenanzahl der einzelnen Foraminiferenarten aus der Foraminiferenanzahl in 1 g Sediment und aus der prozentualen Zusammensetzung der Gesamtfauna errechnet werden. Mit den hier gewonnenen Erkenntnissen wird versucht, die engen Bezichungen zwischen dem prozentualen Anteil der Warmwasserforaminiferen in der Gesamtfauna und dem CO₂-Gehalt des Sedimentes, dieOvey im Kern 241 der schwedischen Albatroß-Expedition beobachtet hat, zu deuten.Herrn Professor Dr.Carl W. Correns zum 60. Geburtstag gewidmet.     

Electron acceleration in solar flares

For the period September 1978 to December 1982 we have identified 55 solar flare particle events for which our instruments on board the ISEE-3 (ICE) spacecraft detected electrons above 10 MeV. Combining our data with those from the ULEWAT spectrometer (MPI Garching and University of Maryland) electron spectra in the range from 0.1 to 100 MeV were obtained. The observed spectral shapes can be divided into two classes. The spectra of the one class can be fit by a single power law in rigidity over the entire observed range. The spectra of the other class deviate from a power law, instead exhibiting a steepening at low rigidities and a flattening at high rigidities. Events with power-law spectra are associated with impulsive (<1 hr duration) soft X-ray emission, whereas events with hardening spectra are associated with long-duration (<1 hr) soft X-ray emission. The characteristics of long-duration events are consistent with diffusive shock acceleration taking place high in the corona. Electron spectra of short-duration flares are well reproduced by the distribution functions derived from a model assuming simultaneous second-order Fermi acceleration and Coulomb losses operating in closed flare loops.     

Chlorit-Hornblende-Felse des Bergsträßer Odenwaldes und ihre Phasenpetrologie

Ultrabasic metamorphic rocks with typical mineral assemblage of cummingtonitic hornblende+Mg-chlorite+talc (described byMatthes u.Okrusch, 1965, and called “hösbachit”) were found for the first time in Odenwald/Germany. Three steps of metamorphic development can be described: the primary magmatic ultrabasic rock consisted of (1) orthopyroxene (bronzite), clinopyroxene (diallage), poikilitic olivine, and some hornblende. This is indicated by textural relicts, structural and geochemical investigations. A regional metamorphic process under conditions of the staurolite-almandine-subfacies ofWinkler’s andTurner andVerhoogen’s almandine-amphibolite facies transformed this assemblage to (2): cummingtonitic hornblende I+Mg-chlorite I (clinochlore)+talc. The third step followed under more diaphthoritic conditions and brought mineral assemblage (3): tremolitic hornblende II+Mg-chlorite II (pennine)+talc.     

Zircon M127 – A Homogeneous Reference Material for SIMS U–Pb Geochronology Combined with Hafnium,Oxygen and,Potentially, Lithium Isotope Analysis

In this article, we document a detailed analytical characterisation of zircon M127, a homogeneous 12.7 carat gemstone from Ratnapura, Sri Lanka. Zircon M127 has TIMS‐determined mean U–Pb radiogenic isotopic ratios of 0.084743 ± 0.000027 for ²⁰⁶Pb/²³⁸U and 0.67676 ± 0.00023 for ²⁰⁷Pb/²³⁵U (weighted means, 2s uncertainties). Its ²⁰⁶Pb/²³⁸U age of 524.36 ± 0.16 Ma (95% confidence uncertainty) is concordant within the uncertainties of decay constants. The δ¹⁸O value (determined by laser fluorination) is 8.26 ± 0.06‰ VSMOW (2s), and the mean ¹⁷⁶Hf/¹⁷⁷Hf ratio (determined by solution ICP‐MS) is 0.282396 ± 0.000004 (2s). The SIMS‐determined δ⁷Li value is ?0.6 ± 0.9‰ (2s), with a mean mass fraction of 1.0 ± 0.1 μg g^?1 Li (2s). Zircon M127 contains ~ 923 μg g^?1 U. The moderate degree of radiation damage corresponds well with the time‐integrated self‐irradiation dose of 1.82 × 10¹⁸ alpha events per gram. This observation, and the (U–Th)/He age of 426 ± 7 Ma (2s), which is typical of unheated Sri Lankan zircon, enable us to exclude any thermal treatment. Zircon M127 is proposed as a reference material for the determination of zircon U–Pb ages by means of SIMS in combination with hafnium and stable isotope (oxygen and potentially also lithium) determination.     

Fe-Ni-Co-O-S Phase Relations in Peridotite-Seawater Interactions

Serpentinization of abyssal peridotites is known to produceextremely reducing conditions as a result of dihydrogen (H₂,aq)release upon oxidation of ferrous iron in primary phases toferric iron in secondary minerals by H₂O. We have compiled andevaluated thermodynamic data for Fe–Ni–Co–O–Sphases and computed phase relations in fO₂,g–fS₂,g andaH₂,aq–aH₂S,aq diagrams for temperatures between 150 and400°C at 50 MPa. We use the relations and compositions ofFe–Ni–Co–O–S phases to trace changesin oxygen and sulfur fugacities during progressive serpentinizationand steatitization of peridotites from the Mid-Atlantic Ridgein the 15°20'N Fracture Zone area (Ocean Drilling ProgramLeg 209). Petrographic observations suggest a systematic changefrom awaruite–magnetite–pentlandite and heazlewoodite–magnetite–pentlanditeassemblages forming in the early stages of serpentinizationto millerite–pyrite–polydymite-dominated assemblagesin steatized rocks. Awaruite is observed in all brucite-bearingpartly serpentinized rocks. Apparently, buffering of silicaactivities to low values by the presence of brucite facilitatesthe formation of large amounts of hydrogen, which leads to theformation of awaruite. Associated with the prominent desulfurizationof pentlandite, sulfide is removed from the rock during theinitial stage of serpentinization. In contrast, steatitizationindicates increased silica activities and that high-sulfur-fugacitysulfides, such as polydymite and pyrite–vaesite solidsolution, form as the reducing capacity of the peridotite isexhausted and H₂ activities drop. Under these conditions, sulfideswill not desulfurize but precipitate and the sulfur contentof the rock increases. The co-evolution of fO₂,g–fS₂,gin the system follows an isopotential of H₂S,aq, indicatingthat H₂S in vent fluids is buffered. In contrast, H₂ in ventfluids is not buffered by Fe–Ni–Co–O–Sphases, which merely monitor the evolution of H₂ activitiesin the fluids in the course of progressive rock alteration.The co-occurrence of pentlandite–awaruite–magnetiteindicates H₂,aq activities in the interacting fluids near thestability limit of water. The presence of a hydrogen gas phasewould add to the catalyzing capacity of awaruite and would facilitatethe abiotic formation of organic compounds. KEY WORDS: serpentinization; ODP Expedition 209; sulfide; oxygen fugacity; sulfur fugacity; hydrothermal system; metasomatism; Mid-Atlantic Ridge     

Better air for better health: Forging synergies in policies for energy access,climate change and air pollution

Air pollution and its related health impacts are a global concern. This paper addresses how current policies on air pollution, climate change and access to clean cooking fuels can effectively reduce both outdoor and household air pollution and improve human health. A state of the art modeling framework is used that combines an integrated assessment model and an atmospheric model to estimate the spatial extent and distribution of outdoor air pollution exposures. Estimates of household energy access and use are modeled by accounting for heterogeneous household energy choices and affordability constraints for rural and urban populations spanning the entire income distribution. Results are presented for 2030 for a set of policy scenarios on air pollution, climate change and energy access and include spatially explicit emissions of air pollutants; ambient concentrations of PM2.5; and health impacts in terms of disability adjusted life years (DALYs) from both ambient and household air pollution. The results stress the importance of enforcing current worldwide air quality legislation in addressing the impacts of outdoor air pollution. A combination of stringent policies on outdoor air pollution, climate change and access to clean cooking fuels is found to be effective in achieving reductions in average ambient PM2.5 exposures to below World Health Organization recommended levels for a majority of the world's population and results in a significant decline in the global burden of disease from both outdoor and household air pollution.     

Impacts of Present and Future Climate Change and Climate Variability on Agriculture in the Temperate Regions: North America

The potential impact of climate variability and climate change on agricultural production in the United States and Canada varies generally by latitude. Largest reductions are projected in southern crop areas due to increased temperatures and reduced water availability. A longer growing season and projected increases in CO₂ may enhance crop yields in northern growing areas. Major factors in these scenarios analyzes are increased drought tendencies and more extreme weather events, both of which are detrimental to agriculture. Increasing competition for water between agriculture and non-agricultural users also focuses attention on water management issues. Agriculture also has impact on the greenhouse gas balance. Forests and soils are natural sinks for CO₂. Removal of forests and changes in land use, associated with the conversion from rural to urban domains, alters these natural sinks. Agricultural livestock and rice cultivation are leading contributors to methane emission into the atmosphere. The application of fertilizers is also a significant contributor to nitrous oxide emission into the atmosphere. Thus, efficient management strategies in agriculture can play an important role in managing the sources and sinks of greenhouse gases. Forest and land management can be effective tools in mitigating the greenhouse effect.