The Quaternary history of the Wash fluvial network, UK

This paper appraises and compares the Middle-Upper Pleistocene sedimentary sequences preserved in the fluvial systems draining into the Fenland Basin and the Wash estuary. Of the main Fenland rivers the longest records, which extend back to the initial Anglian (glacial) formation of the basin, are found in the Great Ouse and its tributaries, particularly the Cam and the Nar. These sequences preserve sediments representing all four post-Anglian interglacials. The Nene also has an extensive post-Anglian history, with evidence for a Hoxnian estuary that is presumed to have been the precursor of the Wash. North of the Nene, however, the Welland and Witham (proto-Trent) have relatively short sequences, which are thought to commence with a later (post-Anglian-pre-Devensian) glaciation that affected Lincolnshire and fed the previously-recognized Tottenhill outwash delta south of Kings Lynn. Prior to Devensian deglaciation the Witham valley was occupied by the Trent, which was the trunk river of the late Middle Pleistocene Wash system. During periods of low sea level the river would have extended north-eastwards across what is now the floor of the North Sea, possibly via the Inner Silver Pit. Several of the central Fenland sequences show evidence of infrequent terrace formation during the late Quaternary, although this might in part be due to poor vertical separation between terraces, so that differentiating them has been difficult; this has been exacerbated by mixed biostratigraphical signals due to the preservation of sediments representing more than one interglacial beneath a single terrace surface. In several of the systems there is evidence for valley rejuvenation to the lowest terrace or valley-floor level during the MIS 4-3 transition. The observed differences within what, during the predominant periods of lower sea level, would have been a single Wash river system are difficult to explain.     

The First Hop: Use of Beaufort Sea Deltas by Hatch-Year Semipalmated Sandpipers

River deltas along Alaska’s Beaufort Sea coast are used by hatch-year semipalmated sandpipers (Calidris pusilla) after leaving their terrestrial natal sites, but the drivers of their use of these stopover sites on the first “hop” of fall migration are unknown. We quantified sandpiper temporal distribution and abundance as related to food resources at three river deltas during the beginning of their fall migration (post-breeding period) to compare the habitat quality among these deltas. We conducted population counts, sampled invertebrates, and captured birds to collect blood samples from individuals for triglyceride and stable isotope analyses to determine fattening rates and diet. Patterns of sandpiper and invertebrate abundance were complex and varied among deltas and within seasons. River deltas were used by sandpipers from late July to late August, and peak sandpiper counts ranged from 1000 to 4000 individuals, of which 98% were hatch-year semipalmated sandpipers. Isotopic signatures from blood plasma samples indicated that birds switched from a diet of upland tundra to delta invertebrate taxa as the migration season progressed, suggesting a dependence on delta invertebrates. Despite differences in diet among deltas, we found no differences in fattening rates of juvenile sandpipers as indicated by triglyceride levels. The number of sandpipers was positively associated with abundance of Amphipoda and Oligochaeta at the Jago and Okpilak-Hulahula deltas; an isotopic mixing model indicated that sandpipers consumed Amphipoda and Oligochaeta at Jago, mostly Chironomidae at Okpilak-Hulahula and Spionidae at Canning. Regardless of the difference in sandpiper diets at the Beaufort Sea deltas, their similar fattening rates throughout the season indicate that all of these stopover sites provide a critical food resource for hatch-year sandpipers beginning their first migration.     

Using FTIR spectroscopy to characterise the soil mineralogy and geochemistry of cryoconite from Aldegondabreen glacier,Svalbard

Mineralogical and geochemical diversity in cryoconite granules from Aldegondabreen glacier was investigated using FTIR spectroscopy. Results suggest that the technique is an effective tool for investigating mineralogy and identifying spatial differences in geochemistry, based upon characteristic spectral signatures.     

Supercritical gas sorption on moist coals

The effect of moisture on the CO₂ and CH₄ sorption capacity of three bituminous coals from Australia and China was investigated at 55 °C and at pressures up to 20 MPa. A gravimetric apparatus was used to measure the gas adsorption isotherms of coal with moisture contents ranging from 0 to about 8%. A modified Dubinin–Radushkevich (DR) adsorption model was found to fit the experimental data under all conditions. Moisture adsorption isotherms of these coals were measured at 21 °C. The Guggenheim–Anderson–de Boer (GAB) model was capable of accurately representing the moisture isotherms over the full range of relative pressures.Moist coal had a significantly lower maximum sorption capacity for both CO₂ and CH₄ than dry coal. However, the extent to which the capacity was reduced was dependent upon the rank of the coal. Higher rank coals were less affected by the presence of moisture than low rank coals. All coals exhibited a certain moisture content beyond which further moisture did not affect the sorption capacity. This limiting moisture content was dependent on the rank of the coal and the sorbate gas and, for these coals, corresponded approximately to the equilibrium moisture content that would be attained by exposing the coal to about 40–80% relative humidity. The experimental results indicate that the loss of sorption capacity by the coal in the presence of water can be simply explained by volumetric displacement of the CO₂ and CH₄ by the water. Below the limiting moisture content, the CO₂ sorption capacity reduced by about 7.3 kg t^− 1 for each 1% increase in moisture. For CH₄, sorption capacity was reduced by about 1.8 kg t^− 1 for each 1% increase in moisture.The heat of sorption calculated from the DR model decreased slightly on addition of moisture. One explanation is that water is preferentially attracted to high energy adsorption sites (that have high energy by virtue of their electrostatic nature), expelling CO₂ and CH₄ molecules.     

Contrasting isotopic signatures between anthropogenic and geogenic Zn and evidence for post-depositional fractionation processes in smelter-impacted soils from Northern France

Zinc isotopes have been studied along two smelter-impacted soil profiles sampled near one of the largest Pb and Zn processing plants in Europe located in northern France, about 50 km south of Lille. Mean δ⁶⁶Zn values along these two soil profiles range from +0.22 ± 0.17‰ (2σ) to +0.34 ± 0.17‰ (2σ) at the lowest horizons and from +0.38 ± 0.45‰ (2σ) to +0.76 ± 0.14‰ (2σ) near the surface. The δ⁶⁶Zn values in the lowest horizons of the soils are interpreted as being representative of the local geochemical background (mean value +0.31 ± 0.38‰), whereas heavier δ⁶⁶Zn values near the surface of the two soils are related to anthropogenic Zn. This anthropogenic Zn occurs in the form of franklinite (ZnFe₂O₄)-bearing slag grains originating from processing wastes at the smelter site and exhibiting δ⁶⁶Zn values of +0.81 ± 0.20‰ (2σ). The presence of franklinite is indicated by EXAFS analysis of the topsoil samples from both soil profiles as well as by micro-XANES analysis of the surface horizon of a third smelter-impacted soil from a distant site. These results indicate that naturally occurring Zn and smelter-derived Zn exhibit significantly different δ⁶⁶Zn values, which suggests that zinc isotopes can be used to distinguish between geogenic and anthropogenic sources of Zn in smelter-impacted soils. In addition to a possible influence of additional past sources of light Zn (likely Zn-sulfides and Zn-sulfates directly emitted by the smelter), the light δ⁶⁶Zn values in the surface horizons compared to smelter-derived slag materials are interpreted as resulting mainly from fractionation processes associated with biotic and/or abiotic pedological processes (Zn-bearing mineral precipitation, Zn complexation by organic matter, and plant uptake of Zn). This conclusion emphasizes the need for additional Zn isotopic studies before being able to use Zn isotopes to trace sources and pathways of this element in surface environments.     

Chemical models of vitrinite reflectance evolution

A global kinetic model of vitrinite reflectance evolution is developed to illustrate a new approach to vitrinite reflectance modelling. The method utilizes quantitative pyrolysisgas Chromatographic data from isolated vitrinite kerogens to derive the concentrations of structurally specific moieties (alkylphenol precursors) in vitrinite kerogens as a function of rank. This data set is used to calibrate a gaussian distributed activation energy model for phenol-precursor loss from vitrinites using published burial histories. Phenol yield is then correlated with vitrinite reflectance. The predictive vitrinite reflectance model based on this phenol system is tested against a well from the US Gulf Coast area, the results being compared with a Lopatin model of the same well. This type of vitrinite reflectance model is numerically compatible with current generation kinetic models of hydrocarbon production from source rock kerogens, and has a better heating rate independence than Lopatin's method.

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Zusammenfassung Um eine neue Annäherung an das Modellieren der Vitrinit-Reflexion zu demonstrieren, wurde ein global-kinetisches Modell der Entwicklung der Vitrinit-Reflexion erstellt. Die Methode verwendet Daten von quantitativer Pyrolyse-Gas Chromatographie isolierten Vitrinitkerogens, um die Konzentration von strukturspezifischen Moieten (Alkylophenol-Vorläufer) in Vitrinitkerogen als Funktion der Reihenfolge zu erhalten. Verwendet werden diese Daten, um ein nach Gauss verteiltes Aktivierungsenergiemodell zu kalibrieren, das mit Hilfe von veröffentlichten Ablagerungsgeschichten den Phenol-Vorläuferverlust von Vitriniten beschreibt. Die Phenol-Ausbeute wird dann mit der Vitrinit-Reflexion korreliert. Das auf dem Phenolsystem basierende Vitrinit-Reflexionsmodell wird in einem Test einem Bohrloch an der amerikanischen Golfküste gegenübergestellt. Die Ergebnisse werden mit dem Lopatinmodell des selben Bohrlochs verglichen. Diese Art eines Vitrinit-Reflexionsmodells ist numerisch wettbewerbsfähig mit der heutigen Generation kinetischer Modelle der Kohlenwasserstofferzeugung aus Trägergesteinskerogenen. Außerdem ist seine Unabhängigkeit von der Erhitzungsrate größer als mit der Lopatin-Methode.

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Résumé L'auteur présente un modèle cinétique global de l'évaluation du pouvoir réflecteur de la vitrinite, afin d'illuster une approche nouvelle dans la modélisation de ce pourvoir réflecteur. Cette méthode utilise des données quantitatives fournies par la pyrolyse combinée à la Chromatographie en phase gazeuse et relatives à des kérogènes de vitrinite. A partir de ces données, on exprime les concentrations des fractions à structure spécifique dans les kérogènes vitrinitiques en fonction du degré d'évolution. A partir de cet ensemble de données, on établit un modèle de l'énergie d'activation selon une distribution gaussienne, applicable à la perte de phénol-précurseur dans les vitrinites, en se référant à cet effet aux déroulements historiques de l'enfouissement fournis par la littérature. La production de phénol est alors mise en relation avec le pourvoir réflecteur de la vitrinite. Le modèle du pouvoir réflecteur prévisible, basé sur ce système des phénols a été contrôlé dans un forage de la côte du golfe du Mexique (USA), et les résultats comparés à ceux du modèle de Lopatin appliqué au même forage. Le modèle présenté est numériquement compatible avec les modèles cinétiques habituels qui rendent compte de la production d'hydrocarbure à partir des kérogènes des roches-mères; il présente une meilleure indépendance que la méthode de Lopatin par rapport au taux d'échauffement.

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Large-strain deformation and strain partitioning in polyphase rocks: Dislocation creep of olivine–magnesiowüstite aggregates

Aggregates composed of olivine and magnesiowüstite have been deformed to large strains at high pressure and temperature to investigate stress and strain partitioning, phase segregation and possible localization of deformation in a polyphase material. Samples with 20 vol.% of natural olivine and 80 vol.% of (Mg_0.7Fe_0.3)O were synthesized and deformed in a gas-medium torsion apparatus at temperatures of 1127 °C and 1250 °C, a confining pressure of 300 MPa and constant angular displacement rates equivalent to constant shear strain rates of 1–3.3 × 10^− 4 s^− 1. The samples deformed homogeneously to total shear strains of up to γ  15. During constant strain rate measurements the flow stress remained approximately stable at 1250 °C while it progressively decreased after the initial yield stress at the lower temperature. Mechanical data, microstructures and textures indicate that both phases were deforming in the dislocation creep regime. The weaker component, magnesiowüstite, controlled the rheological behavior of the bulk material and accommodated most of the strain. Deformation and dynamic recrystallization lead to grain refinement and to textures that were not previously observed in pure magnesiowüstite and may have developed due to the presence of the second phase. At 1127 °C, olivine grains behaved as semi-rigid inclusions rotating in a viscous matrix. At 1250 °C, some olivine grains remained largely undeformed while deformation and recrystallization of other grains oriented for a-slip on (010) resulted in a weak foliation and a texture typical for pure dry olivine aggregates. Both a-slip and c-slip on (010) were activated in olivine even though the nominal stresses were up to 2 orders of magnitude lower than those needed to activate these slip systems in pure olivine at the same conditions.     

Symphurus civitatium (Pleuronectiformes: Cynoglossidae), a second estuarine-occurring tonguefish off the Southeastern United States and Northern Gulf of Mexico

Two species of tonguefishes,Symphurus plagiusa (Linnaeus 1766) andSymphurus civitatium Ginsburg 1951, occur sympatrically and sometimes syntopically in shallow water habitats in North Carolina and Louisiana estuaries. In North Carolina, approximately 2% of 430 small (<75 mm SL) tonguefishes collected wereS. civitatium, while in Barataria Bay, Louisiana, this species was more abundant and cosmopolitan in distribution than wasS. plagiusa, comprising over 82% of 3,564 tonguefishes collected with a small beam trawl over a 2-yr period. Historical literature has regardedS. plagiusa as the only tonguefish species inhabiting inshore waters in both regions. Presence of a secondSymphurus species in shallow estuaries has been overlooked, most probably due to difficulties in identifying early post-settlement juveniles because both species have similar morphologies and overlapping dorsal-fin and anal-fin ray counts. Juveniles can be readily recognized by differences in number of caudal-fin rays (10 inS. plagiusa versus 12 inS. civitatium), especially when used in combination with pigmentation patterns and posterior extent of the jaws relative to the posterior margin of the lower eye. The most distinctive pigmentation difference between juveniles of these two species (allowing for accurate identifications of over 98% of juveniles) is the absence inS. civitatium (12–61 mm SL) of a series of melanophores overlying pterygiophore regions of the dorsal and anal fins on the blind side. This feature contrasts markedly with that of juvenileS. plagiusa (12–65 mm SL), which are characterized by two interrupted, diagonal series of dark chromatophores converging, but not merging, with posterior tapering of the body. Occurrence of two sympatric species of tonguefishes in estuarine environments in the northcentral Gulf of Mexico and southeastern U.S. potentially compromises results of earlier ecological and distributional studies that assumed presence of only a single tonguefish species in these regions.     

Smart optics in ast

Smart optics means much more than adaptive optics on telescopes: these new technologies are changing the way space instruments are built and operated and are bringing new technologies into everyday life in the form of cheaper, lighter and more robust optical systems. Steve Welch, Peter Doel, Alan Greenaway and Gordon Love summarize the work of the Smart Optics Faraday Partnership in the UK.     

Carbon Sequestration in Arable Soils is Likely to Increase Nitrous Oxide Emissions,Offsetting Reductions in Climate Radiative Forcing

Strategies for mitigating the increasing concentration of carbon dioxide (CO₂) in the atmosphere include sequestering carbon (C) in soils and vegetation of terrestrial ecosystems. Carbon and nitrogen (N) move through terrestrial ecosystems in coupled biogeochemical cycles, and increasing C stocks in soils and vegetation will have an impact on the N cycle. We conducted simulations with a biogeochemical model to evaluate the impact of different cropland management strategies on the coupled cycles of C and N, with special emphasis on C-sequestration and emission of the greenhouse gases methane (CH₄) and nitrous oxide (N₂O). Reduced tillage, enhanced crop residue incorporation, and farmyard manure application each increased soil C-sequestration, increased N₂O emissions, and had little effect on CH₄ uptake. Over 20 years, increases in N₂O emissions, which were converted into CO₂-equivalent emissions with 100-year global warming potential multipliers, offset 75–310% of the carbon sequestered, depending on the scenario. Quantification of these types of biogeochemical interactions must be incorporated into assessment frameworks and trading mechanisms to accurately evaluate the value of agricultural systems in strategies for climate protection.