Variability of Fram Strait sea ice export: causes, impacts and feedbacks in a coupled climate model

Analyses of a 500-year control integration of the global coupled atmosphere–sea ice–ocean model ECHAM5.0/MPI-OM show a high variability in the ice export through Fram Strait on interannual to decadal timescales. This variability is mainly determined by variations in the sea level pressure gradient across Fram Strait and thus geostrophic wind stress. Ice thickness anomalies, formed at the Siberian coast and in the Chukchi Sea, propagate across the Arctic to Fram Strait and contribute to the variability of the ice export on a timescale of about 9 years. Large anomalies of the ice export through Fram Strait cause fresh water signals, which reach the Labrador Sea after 1–2 years and lead to significant changes in the deep convection. The associated anomalies in ice cover and ocean heat release have a significant impact on air temperature in the Labrador Sea and on the large-scale atmospheric circulation. This affects the sea ice transport and distribution in the Arctic again. Sensitivity studies, simulating the effect of large ice exports through Fram Strait, show that the isolated effect of a prescribed ice/fresh water anomaly is very important for the climate variability in the Labrador Sea. Thus, the ice export through Fram Strait can be used for predictability of Labrador Sea climate up to 2 years in advance.     

Stratigraphy of nutrients and metals in sediment profiles of two dimictic lakes in North-Eastern Germany

A sedimentological study of two dimitic lakes in North-Eastern Germany provided a record of anthropogenic impacts and historical changes of water quality. The upper 50 cm sediment profiles were compared for major nutrients and selected major trace elements. The sediments were dated by ²¹⁰Pb and ¹³⁷Cs measurement. The upper 50 cm sediment profiles represent approximately the last 100 years of history in both lakes. Element analyses show different characteristic stratigraphic patterns in both lakes. Based on the nutrient and metal stratification, three characteristic time periods can be documented for both lakes. In addition to agricultural use of the catchment area, atmospheric pollution greatly influenced the metal concentration in the sediment layers. Variation in the external loading and redox conditions in the hypolimnion explain the variation in the composition and accumulation of metals in the sediment stratigraphy. No increases or changes in the trophic level of either lake could be documented based on the accumulation of the nutrients C, N and P. The ratio of Fe/Mn and Fe/Ca characterized the changing redox conditions. The stratigraphy of Pb and Zn agrees with the historical variation in atmospheric pollution and confirms literature values for Central and North Europe. The drop in Pb and Zn over the last 10–15 years is a regional effect in North-Eastern Germany.     

Sedimentology of a debris‐rich,perhumid valley glacier margin in the Rakaia Valley,South Island,New Zealand

The sedimentology and stratigraphy of a multi‐phase glaciation sequence dating to Marine Isotope Stage 6 in the Rakaia Valley, South Island, New Zealand, is presented. This outcrop presents an example of the depositional signature of an end member of temperate valley glaciation, where voluminous sediment supply in a tectonically active setting combines with high annual temperatures and low seasonality to generate significant year‐round glacifluvial activity. Such glacial systems produce geological–climatic units that are dominated by thick sequences of aggradational gravels and proglacial lake sediments trapped behind outwash heads during deglaciation. At Bayfields Cliff, outwash sequences record an oscillating glacier margin marked by a sequence of glacier‐fed, Gilbert‐type deltas. The deltas are cut by numerous small‐scale, syndepositional, normal faults indicating both loss of glacier support and melt‐out of buried ice. A larger‐scale thrust fault system reflects late‐stage ice overrun. Braid plain gravels and chaotic disturbed glacial lake sediments are also recorded. A notable feature of these systems is the virtual absence of till in an environment with much other evidence for proximal ice. Cumulatively we regard these sediment–landform associations as diagnostic of debris‐laden, perhumid, temperate valley glacier systems. Copyright © 2012 John Wiley & Sons, Ltd.     

The crystal structure of cualstibite-1M (formerly cyanophyllite), its revised chemical formula and its relation to cualstibite-1T

The crystal structure of the rare secondary mineral cualstibite-1M (formerly cyanophyllite), originally reported to have the chemical formula 10CuO·2Al₂O₃·3Sb₂O₃·25H₂O and orthorhombic symmetry, was solved from single-crystal intensity data (Mo-Kα X-radiation, CCD area detector, 293 K, 2θ_max?=?80) collected on a twinned crystal containing very minor Mg. The mineral is monoclinic, P2₁/c (no. 14), with a?=?9.938(1), b?=?8.890(1), c?=?5.493(1) Å, β?=?102.90(1)°, V?=?473.05(11) ų; R1(F)?=?0.0326. All crystals investigated turned out to be non-merohedric twins. The atomic arrangement has a distinctly layered character. Brucite-like sheets composed of two [4?+?2]-coordinated (Cu,Al,Mg) sites are linked by weak hydrogen-bonding (O···O?~?2.80 Å) to isolated regular Sb(OH)₆ octahedra (<Sb-O>?=?1.975 Å). The layered, pseudotrigonal character explains the perfect cleavage and the proneness to twinning. The Sb site is fully occupied and the two (Cu,Al,Mg) sites have occupancies of Cu_0.79Al_0.17Mg_0.04 and Cu_0.72Al_0.23Mg_0.05. The Cu-richer site shows a slightly stronger Jahn-Teller-distortion. The resulting empirical formula, which necessitates a H₂O-for-OH substitution to obtain charge balance, is (Cu_2.23Al_0.63Mg_0.14)(OH)_5.63(H₂O)_0.37[Sb⁵⁺(OH)₆]. The ideal chemical formula is (Cu,Al)₃(OH)₆[Sb⁵⁺(OH)₆], with Cu:Al = 2:1. The structure is closely related to those of trigonal cualstibite-1T [Cu₂AlSb(OH)₁₂, P-3, with ordered Cu-Al distribution in the brucite sheets], and its Zn analogue zincalstibite-1T [Zn₂AlSb(OH)₁₂]. Cualstibite-1M and cualstibite-1T are polytypes and, together with zincalstibite-1T, zincalstibite-9R and omsite, belong to the cualstibite group within the hydrotalcite supergroup, which comprises all natural members of the large family of layered double hydroxides (LDH).     

Combined Li-He isotopes in Iceland and Jan Mayen basalts and constraints on the nature of the North Atlantic mantle

Lithium (Li) isotopes are thought to provide a powerful proxy for the recycling of crustal material, affected by low temperature alteration, through the mantle. We present Li isotope compositions for basaltic volcanic rocks from Hengill, Iceland, and Jan Mayen in order to examine possible links between ocean island volcanism and recycled oceanic crust and to address recent suggestions that mantle ³He/⁴He is also related to recycling of ancient slabs. Basaltic glasses spanning a range of chemical enrichment from the Hengill fissure system define an inverse correlation between δ⁷Li (3.8-6.9‰) and ³He/⁴He (12-20 R_A). The high-³He/⁴He basalts have low δ¹⁸O as well as excess Eu and high Nb/U, but carry no Li isotope evidence of being the product of recycling of altered slab or wedge material. In fact, there is no clear correlation between Li or He isotopes on the one hand and any of the other fingerprints of recycled slab components. The low-³He/⁴He samples do have elevated Nb/U, Sr/Nd, positive Eu anomalies and high δ⁷Li (∼6.9‰), providing evidence of a cumulate-enriched source that could be part of an ancient altered ocean floor slab.Basalts from Jan Mayen are characterized by large degrees of enrichment in incompatible trace elements typical of EM-like basalts but have homogeneous δ⁷Li typical of depleted mantle (3.9-4.7‰) providing evidence for a third mantle source in the North Atlantic. It appears that oceanic basalts can display a wide range in isotope and trace element compositions associated with recycled components whilst exhibiting no sign of modern surface-altered slab or wedge material from the Li isotope composition.     

Spectral analyses of [WCL]-type central stars

The optical spectra of the seven late-type Wolf-Rayet central stars NGC-40 (PNG 120.0+09.8, subtype [WC8]), He 2-99 (PNG 309.0–04.2, [WC9]), BD+30°3639 (PN G 064.7+05.0, [WC9]), CPD-56°8032 (PNG 332.9–09.9, [WC11]), He2-113 (PNG 321.0+03.9, [WC11]), M4-18 (PNG 146.7+07.6, [WC11]) and K2-16 (PNG 352.9+11.4, [WC11]) are analyzed by means of spherically expanding model atmospheres. The NLTE simulations account for the elements hydrogen, helium, carbon and oxygen. As main results effective temperature, element abundances and final velocity of the wind are determined for each star. Assuming distances or luminosities for the objects, also the stellar radii and the mass-loss rates can be fixed. The results of these analyses establish empirical constraints for the evolutionary status of WC-type central stars as post-AGB objects and provide input for modeling their planetary nebulae.     

Major and trace elements in German bottled water,their regional distribution,and accordance with national and international standards

The market for mineral water has been growing steadily over the last few years. Germany is the country with the highest number of bottled mineral water brands (908 bottled water samples from 502 wells/brands were analyzed). The per capita consumption of mineral water in Germany in 2003 was 129 L. A wide range of values of one to seven orders of magnitude was determined for 71 elements in the bottled water samples analyzed by ICP-QMS, ICP-AES, IC, titration, photometric, conductometric and potentiometric methods. A comparison of the element concentrations and the legal limits for both bottled and tap water (EU, Germany, US EPA, WHO) shows that only 70% of the 908 mineral water samples fulfill the German and EU drinking water (i.e., tap water) regulations for all parameters (not including pH) for which action levels are defined. Nearly 5% of the bottled water samples not fulfill the German and EU regulations for mineral and table water. Comparison of our results with the current German and European action levels for mineral and table water shows that only 42 of the bottled water samples exceed the limits for one or more of the following elements: arsenic, nitrate, nitrite, manganese, nickel and barium concentrations. Ten of the bottled water samples contain uranium concentrations above the 10 μg/L recommended limit.     

Methane emission measurements in urban areas in Eastern Germany

We have investigated methane emissions from urban sources in the former East Germany using innovative measurement techniques including a mobile real-time methane instrument and tracer release experiments. Anthropogenic and biogenic sources were studied with the emphasis on methane emissions from gas system sources, including urban distribution facilities and a production plant. Methane fluxes from pressure regulating stations ranged from 0.006 to 24. l/min. Emissions from diffuse sources in urban areas were also measured with concentration maps and whole city flux experiments. The area fluxes of the two towns studied were 0.37 and 1.9 g/m²/s. The emissions from individual gas system stations and total town emissions of this study are comparable to results of similar sites examined in the United States.     

The Sabzevar blueschists of the North-Central Iranian micro-continent as remnants of the Neotethys-related oceanic crust subduction

The Sabzevar ophiolites mark the Neotethys suture in east-north-central Iran. The Sabzevar metamorphic rocks, as part of the Cretaceous Sabzevar ophiolitic complex, consist of blueschist, amphibolite and greenschist. The Sabzevar blueschists contain sodic amphibole, epidote, phengite, calcite ± omphacite ± quartz. The epidote amphibolite is composed of sodic-calcic amphibole, epidote, albite, phengite, quartz ± omphacite, ilmenite and titanite. The greenschist contains chlorite, plagioclase and pyrite, as main minerals. Thermobarometry of a blueschist yields a pressure of 13–15.5 kbar at temperatures of 420–500 °C. Peak metamorphic temperature/depth ratios were low (~12 °C/km), consistent with metamorphism in a subduction zone. The presence of epidote in the blueschist shows that the rocks were metamorphosed entirely within the epidote stability field. Amphibole schist samples experienced pressures of 5–7 kbar and temperatures between 450 and 550 °C. The presence of chlorite, actinolite, biotite and titanite indicate greenschist facies metamorphism. Chlorite, albite and biotite replacing garnet or glaucophane suggests temperatures of >300 °C for greenschist facies. The formation of high-pressure metamorphic rocks is related to north-east-dipping subduction of the Neotethys oceanic crust and subsequent closure during lower Eocene between the Central Iranian Micro-continent and Eurasia (North Iran).