Variability and propagation of Labrador Sea Water in the southern subpolar North Atlantic

The variability of two modes of Labrador Sea Water (LSW) (upper and deep Labrador Sea Water) and their respective spreading in the interior North Atlantic Ocean are investigated by means of repeated ship surveys carried out along the zonal WOCE line A2/AR19 located at 43–48°N (1993–2007) and along the GOOS line at about 48–51°N (1997–2002). Hydrographic section data are complemented by temperature, salinity, and velocity time series recorded by two moorings. They have been deployed at the western flank of the Mid-Atlantic Ridge (MAR) in the Newfoundland Basin during 1996–2004. The analysis of hydrographic anomalies at various longitudes points to a gradual eastward propagation of LSW-related signals, which happens on time scales of 3–6 years from the formation region towards the MAR. Interactions of the North Atlantic Current (NAC) with the Deep Western Boundary Current (DWBC) close to Flemish Cap point to the NAC being the main distributor of the different types of LSW into the interior of the Newfoundland Basin. Comparisons between the ship data and the mooring records revealed that the mooring sites are located in a region affected by highly variable flow. The mooring time series demonstrate an elevated level of variability with eddy activity and variability associated with the NAC considerably influencing the LSW signals in this region. Hydrographic data taken from Argo profiles from the vicinity of the mooring sites turned out to mimic quite well the temporal evolution captured by the moorings. There is some indication of occasional southward flow in the LSW layer near the MAR. If this can be considered as a hint to an interior LSW-route, it is at least of minor importance in comparison to the DWBC. It acts as an important supplier for the interior North Atlantic, distributing older and recently formed LSW modes southward along the MAR.     

Stable carbon isotopic ratios of CH4-CO2-bearing fluid inclusions in fracture-fill mineralization from the Lower Saxony Basin (Germany) - A tool for tracing gas sources and maturity

The stable carbon isotopic ratios (δ¹³C) of methane (CH₄) and carbon dioxide (CO₂) of gas-rich fluid inclusions hosted in fracture-fill mineralization from the southern part of the Lower Saxony Basin, Germany have been measured online using a crushing device interfaced to an isotopic ratio mass spectrometer (IRMS). The data reveal that CH₄ trapped in inclusions seems to be derived from different source rocks with different organic matter types. The δ¹³C values of CH₄ in inclusions in quartz hosted by Carboniferous rocks range between −25 and −19‰, suggesting high-maturity coals as the source of methane. Methane in fluid inclusions in minerals hosted by Mesozoic strata has more negative carbon isotope ratios (−45 to −31‰) and appears to represent primary cracking products from type II kerogens, i.e., marine shales. There is a positive correlation between increasing homogenization temperatures of aqueous fluid inclusions and less negative δ¹³C(CH₄) values of in co-genetic gas inclusions probably indicating different mtaturity of the potential source rocks at the time the fluids were released. The CO₂ isotopic composition of CH₄-CO₂-bearing inclusions shows slight negative or even positive δ¹³C values indicating an inorganic source (e.g., water-rock interaction and dissolution of detrital, marine calcite) for CO₂ in inclusions. We conclude that the δ¹³C isotopic ratios of CH₄-CO₂-bearing fluid inclusions can be used to trace migration pathways, sources of gases, and alteration processes. Furthermore, the δ¹³C values of methane can be used to estimate the maturity of the rocks from which it was sourced. Results presented here are further supported by organic geochemical analysis of surface bitumens which coexist with the gas inclusion-rich fracture-fill mineralization and confirm the isotopic interpretations with respect to fluid source, type and maturity.     

Future emissions of marine halogenated very-short lived substances under climate change

Halogenated Very Short-lived Substances (VSLS), such as bromoform, dibromomethane and methyl iodide, are naturally produced in the oceans and are involved in ozone depletion in the troposphere and the stratosphere. The effect of climate change on the oceanic emissions of these compounds is not well quantified. Based on present-day observed global oceanic and atmospheric concentrations, and historic and future data from three CMIP5 models, past and future sea-to-air fluxes of these VSLS are calculated. The simulations are used to infer possible effects of projected changes of physical forcing on emissions in different oceanic regimes. CMIP5 model output for 1979–2100 from the historical scenario and the RCP scenarios 2.6 and 8.5 are used as input data for the emission calculations. Of the parameters that have the main influence on the sea-to-air fluxes, the global sea surface temperatures show a steady increase during the twenty-first century, while the projected changes of sea surface wind speed is very small. The calculated emissions based on the historical CMIP5 model runs (1979–2005) increased over the 26 year period and agree well with the emissions based on ERA-Interim data. The future sea-to-air fluxes of VSLS generally increase during the twenty-first century under the assumption of constant concentration fields in the ocean and atmosphere. The multi-model mean global emissions of bromoform increase by 29.4% (9.0%) between 1986 and 2005 and 2081–2100 under RCP 8.5 (2.6) and dibromomethane and methyl iodide emissions increase by 23.3% (6.4%) and 5.5% (1.5%), respectively. Uncertainties of the future emission estimates, driven by ongoing environmental changes such as changing oceanic productivity (not considered in this study) are discussed.     

Characterization of sediments in an abandoned mining area; a case study of Mansfeld region,Germany

The distribution of selected heavy metals, including some radionuclides, metalloids and non-metals was determined in stream sediments in a region influenced by abandoned copper mining and ore processing activities. A considerable amount of the ore processing waste with a very complex composition and highly elevated concentrations of zinc, sulfur, lead, copper, arsenic, and a lot of other elements in the range between 100 and 1,000 mg/kg (Sb, Mn, Ni, Cr, Cd, Hg, and Ag) was piled up on mine dumps. The dispersion of the pollutants originating from this source and their environmental impact were investigated. Both, sediments and original waste material were studied to indicate the pathways and the mobilization behavior of different pollutants. For this purpose, the process of the elution of pollutants by application of different fractionation schemes was studied. The capabilities of different analytical techniques are shown for the analysis of solid samples (X-ray fluorescence spectrometry, Gamma-spectrometry) and liquid ones (ICP-atomic emission spectrometry, ICP-mass spectrometry and different techniques of atomic absorption). Additionally, the coupling of ion chromatography and ICP-MS detection was used to study the distribution of arsenic species in the sediment cores of a lake which acts as a natural sink for the region.     

Geomicrobiology of Blood Falls: An Iron-Rich Saline Discharge at the Terminus of the Taylor Glacier, Antarctica

Blood Falls, a saline subglacial discharge from the Taylor Glacier, Antarctica provides an example of the diverse physical and chemical niches available for life in the polar desert of the McMurdo Dry Valleys. Geochemical analysis of Blood Falls outflow resembles concentrated seawater remnant from the Pliocene intrusion of marine waters combined with products of weathering. The result is an iron-rich, salty seep at the terminus of Taylor Glacier, which is subject to episodic releases into permanently ice-covered Lake Bonney. Blood Falls influences thegeochemistry of Lake Bonney, and provides organic carbon and viable microbes to the lakesystem. Here we present the first data on the geobiology of Blood Falls and relate it totheevolutionary history of this unique environment. The novel geological evolution of thissubglacial environment makes Blood Falls an important site for the study of metabolic strategiesin subglacial environments and the impact of subglacial efflux on associated lake ecosystems.     

Salt-water intrusion and nitrate contamination in the Valley of Hermosillo and El Sahuaral coastal aquifers, Sonora, Mexico

 The Valley of Hermosillo coastal aquifer, state of Sonora, northwestern Mexico, has been over-exploited for the last four decades, in order to maintain agricultural activity in one of the most important irrigation districts of the Mexican Republic. The over-exploitation has resulted in the development of several drawdown cones and in the lowering of the water table to as much as 50 m below mean sea level. Contamination of the aquifer in the form of salt-water intrusion from the Gulf of California and high nitrate concentrations is the consequence of human activities. A hydrogeochemical zonation of the aquifer, based on the presence of different water families, led to the identification of a coastal band approximately 30 km wide that is affected by salt-water intrusion. Conductivity of the sampled water and the interpretation of the ratio Na/Cl×1000 was used to identify the location of three major intrusion plumes in this coastal band. The background nitrate contamination of the aquifer is about 4 ppm, but contents as great as about 17 ppm occur in some wells. Irrigation with raw sewage and movement of contaminants in areas of high hydraulic gradients within the drawdown cones probably are responsible for localized peaks of the nitrate concentration. Received, October 1996 Revised, September 1997, May 1998 Accepted, July 1998     

Boundary-layer observations over water and arctic sea-ice during on-ice air flow

Observations made on 8 and 9 May 1988 by aircraft and two ships in and around the marginal ice zone of the Fram Strait during on-ice air flow under cloudy and cloud-free conditions are presented.The thermodynamic modification of the air mass moving from the open water to the ice over horizontal distances of 100–300 km is only a few tenth of a degree for temperature and a few tenth of a gram per kilogram for specific humidity. This is due to the small temperature differences between sea and ice surfaces. During the day, the ice surface is even warmer than the sea surface. The stably stratified 200–400 m deep boundary layer is often topped by a moisture inversion leading to downward fluxes of sensible as well as latent heat.The radiation and energy balance at the surface are measured as functions of ice cover, cloud cover and sun elevation angle. The net radiationR _Nis the dominating term of the energy budget. During the day, the difference ofR _Nbetween clear and overcast sky is only a few W/m² over ice, but 100–200 W/m² over water. During the night,R _Nover ice is more sensitive to cloud cover.The kinematic structure is characterized by strong shears of the longitudinal and the transversal wind component. The profile of the latter one shows an inflection point near the top of the boundary layer. Dynamically-driven roll circulations are numerically separated from the mean flow. The secondary flow patterns have wavelengths of about 1 km and contribute substantially to the total variances and covariances.     

Significance of polycyclic aromatic hydrocarbons (PAHs) in Permian/Triassic boundary sections

In this study the abundances of several polycyclic aromatic hydrocarbons (PAHs Table 1, I–XXI) have been measured throughout three Permian/Triassic (P/Tr) sections from Meishan (South China), Kap Stosch area (East Greenland) and Peace River Basin (Western Canada). Dibenzothiophene (I) and dibenzofuran (II) were found to decrease in abundance just before or shortly after the P/Tr transition in all three sections while perylene (III) was observed to increase in abundance at the onset of the main extinction horizon (bed 25) in Meishan. Perylene has been attributed to a wood degrading fungal source and, therefore, it seems possible these phenomena are related to the demise of land plants. Further, distinct patterns of various combustion-derived PAHs occurring in each section imply that forest fire events occurred within the Late Permian and Early Triassic. In the Meishan section high amounts of combustion-derived PAHs [pyrene (IV), fluoranthene (V), benzo[a]anthracene (VI), benzofluoranthenes (sum, i.e. VII), benzo[a]pyrene (VIII), benzo[e]pyrene (IX) and coronene (X)] occur within bed 25, also containing ash attributed to the fallout from massive volcanic eruptions in Siberia and/or China.