The Upper Neoproterozoic-Lower Cambrian of the Central Iberian Zone, Spain: chemical and isotopic (Sm-Nd) evidence that the sedimentary succession records an inverted stratigraphy of its source

The Upper Neoproterozoic-Lower Cambrian sedimentary succession in the Central Iberian Zone has recently been divided into 12 sedimentary units (I to XII). Units I to IV are of Late Neoproterozoic age, and units V to XII are Early Cambrian.Throughout the stratigraphic section, shales with similar ranges of SiO₂ and Al₂O₃ have TiO₂ and Zr contents that are coupled and vary gradually from the bottom (unit I, TiO₂ = 1.0-1.1%, Zr = 245-287 ppm) to the top (unit XII, TiO₂ = 0.74-0.86%, Zr = 141-192 ppm). These two parameters clearly distinguish Upper Neoproterozoic from Lower Cambrian compositions, as do certain elemental ratios (Al₂O₃/TiO₂, Rb/Zr, Nb/Ti), which vary from low values at the bottom of the section to high at the top. However, other elements (the rare earth elements [REEs], Y) do not fit this general trend, with heavy REEs and Y showing extreme concentrations in some Lower Cambrian units, which also have negative Ce anomalies.Units I to III and units XI to XII have uniform T_DM neodymium model ages (∼1.1 and 1.7 Ga, respectively), but the units between these two groups have erratic values between 1.4 Ga (unit VII) and 3.4 Ga (unit VIII). Thus, the bottom and top units have neodymium isotope ratios that indicate the presence of two source compositions: a composition that records a juvenile contribution younger than 1.1 Ga and a composition mainly derived from an old basement. Some samples from Lower Cambrian units have disturbed REE abundances and neodymium isotope ratios that are attributed to extensive chemical alteration that resulted in REE and Y redistribution. This alteration probably affected the material now preserved as unit IV during a period of relative sea level fall at the end of the Late Neoproterozoic. Both elemental and isotopic results support the suggestion that the Upper Neoproterozoic-Lower Cambrian stratigraphic section records an inverse stratigraphy of a source hinterland composed of a cover sequence of relatively juvenile crustal materials underlain by an older basement. Through time, the deeper crust gradually increased its contribution to the sediments in the basin from Late Neoproterozoic to Lower Cambrian times. These results are compatible with data from many other European zones.     

In situ sampling reveals rapid uptake and depuration of polycyclic aromatic hydrocarbons by surf clams (Paphies subtriangulata) affected by the Rena oil spill

ABSTRACT

To investigate the uptake and depuration of polycyclic aromatic hydrocarbons associated with the Rena oil spill we sampled the surf clam Paphies subtriangulata at two open coast locations (6?km apart) just prior to oil coming ashore (7 October 2011), then at 1–3 week intervals for the next 4 months. Total polycyclic aromatic hydrocarbons (tPAH) increased at both sites from 1 to 96–124?µg?kg^?1 (wet weight) by 18 October before declining to low levels (<4?µg?kg^?1) by February 2012. Ongoing sampling throughout 2012–2014 included three additional sites to the north east (up to 30?km away) and a site 5?km to the south east revealing tPAH levels generally <10?µg?kg^?1 except in October 2013 where levels ranged between 39–45?µg?kg^?1 at all sites. A comparison of PAH component profiles with oil-contaminated beach sediment indicated that the high levels observed in surf clams between October–December 2011 were clearly associated with the Rena spill. However, the October 2013 peak had a PAH profile inconsistent with weathered Rena oil, suggesting an alternative source of contamination. Our results highlight the potential for P. subtriangulata as a PAH monitoring tool but recognise more study is needed to better quantify baseline levels and uptake and depuration dynamics.     

Migration and speciation transformation mechanisms of mercury in undercurrent zones of the Tongguan gold mining area,Shaanxi Loess Plateau and impact on the environment

In order to study the migration and transformation mechanism of Hg content and occurrence form in subsurface flow zone of gold mining area in Loess Plateau and its influence on water environment, the field in-situ infiltration test and laboratory test were carried out in three typical sections of river-side loess, alluvial and proluvial strata in Tongguan gold mining area of Shaanxi Province, and the following results were obtained: (1) The source of Hg in subsurface flow zone is mainly caused by mineral processing activities; (2) the subsurface flow zone in the study area is in alkaline environment, and the residual state, iron and manganese oxidation state, strong organic state and humic acid state of mercury in loess are equally divided in dry and oxidizing environment; mercury in river alluvial or diluvial strata is mainly concentrated in silt, tailings and clayey silt soil layer, and mercury has certain stability, and the form of mercury in loess is easier to transform than the other two media; (3) under the flooding condition, most of mercury is trapped in the silt layer in the undercurrent zone where the sand and silt layers alternate with each other and the river water and groundwater are disjointed, and the migration capacity of mercury is far less than that of loess layer and alluvial layer with close hydraulic connection; (4) infiltration at the flood level accelerates the migration of pollutants to the ground; (5) the soil in the undercurrent zone is overloaded and has seriously exceeded the standard. Although the groundwater monitoring results are safe this time, relevant enterprises or departments should continue to pay attention to improving the gold extraction process, especially vigorously rectify the small workshops for illegal gold extraction and the substandard discharge of the three wastes, and intensify efforts to solve the geological environmental problems of mines left over from history. At present, the occurrence form of mercury in the undercurrent zone is relatively stable, but the water and soil layers have been polluted. The risk of disjointed groundwater pollution can not be ignored while giving priority to the treatment of loess and river alluvial landform areas with close hydraulic links. The research results will provide a scientific basis for water conservancy departments to groundwater prevention and control in water-deficient areas of the Loess Plateau.     

Petrogenesis of late stage magmatism at Hold with Hope, East Greenland

The Myggbukta caldera complex and a swarm of basic dykes constitute the latest Tertiary magmatism in the Hold with Hope region, East Greenland. The Sr and Nd isotope ratios of these rocks show coherent variations which extend to high ⁸⁷Sr/⁸⁶Sr and low ¹⁴³Nd/¹⁴⁴Nd values and require a contribution from continental lithosphere. Broad correlations with major element differentiation indices suggest that the continental component was incorporated during magmatic differentiation thereby favouring a crustal contamination process. Trace element concentrations are strongly correlated with isotopic compositions but display ranges for many incompatible elements which extend beyond likely crustal contaminant compositions. This is readily modelled by AFC processes in which the dominant cause of trace element enrichment is the concentration effect of fractional crystallisation rather than the composition of the contaminant. The simplest such models still require unrealistically high degrees of fractional crystallisation to explain the ten-fold enrichment of some trace elements. This can be overcome if the primary magmas entering the crust already had highly variable trace element compositions. Such variability is readily achieved if melts from different parts of the melting column escape without thorough homogenization. An AFC model which incorporates variability in parental magma composition is then able to simulate the range of compositions observed at Hold with Hope. This carries the implication that the variations observed are more readily attributed to changes in uncontaminated parental magma than to variations in the composition or amount of contaminant. Received: 5 March 1998 / Accepted: 16 June 1998     

赣南地区石雷石英闪长岩的成因:岩石化学、副矿物微量元素、锆石U-Pb年代学与Sr-Nd-Hf同位素制约

石雷石英闪长岩是赣南崇-余-犹地区比较特殊的闪长质侵入体。锆石的原位U-Pb定年表明,该岩体侵位于433.5±3.4Ma。全岩主量元素特征上显示出中偏酸性(SiO2=56.92%～64.70%),富Al(Al2O3=14.10%～14.83%),富碱(Alk=6.41%～7.40%)特别是富钾(K2O=3.86%～4.85%),镁、铁含量较高,MgO:3.47%～5.95%,FeOT:5.23%～8.14%以及低磷(P2O5=0.27%～0.4%)的特点;微量元素上主要富集K、Rb、Cs等大离子亲石元素和轻稀土元素,亏损Nb、Ta、Ti、P等高场强元素。磷灰石微量元素特征上显示高度富集稀土元素特别是轻稀土元素的特征;具有Eu的负异常(δEu=0.37～0.45)。ISr位于0.7073～0.7132之间,εNd(t)变化于-8.41～-4.97之间,两阶段钕模式年龄介于1.58～1.86Ga之间,Hf同位素组成相对均一,εHf(t)主要集中变化于-8～-2之间,两阶段Hf模式年龄加权平均为1.77±0.09Ga,这些特征都暗示了该石英闪长质岩体的形成是强烈壳幔相互作用的产物,区内加里东晚期可能发生了局部的岩石圈的减薄。     

Cape cormorants decrease,move east and adapt foraging strategies following eastward displacement of their main prey

Numbers of Cape cormorants Phalacrocorax capensis breeding in South Africa decreased by nearly 50% from approximately 107 000 pairs in 1977–1981 to 57 000 pairs in 2010–2014. Although four colonies had >10 000 pairs in 1977–1981, there was just one such colony in 2010–2014. Almost all the decrease occurred after the early 1990s off north-west South Africa, between the Orange River estuary and Dassen Island. South of this, the number breeding in the two periods was stable, with some colonies being formed or growing rapidly in the 2000s. The proportion of South Africa’s Cape cormorants that bred south of Dassen Island increased from 35% in 1977–1981 to 66% in 2010–2014, with the opposite situation observed in the north-west. This matched a shift to the south and east in the distributions of two of the Cape cormorant’s main prey species, anchovy Engraulis encrasicolus and sardine Sardinops sagax. In 2014, an apparent scarcity of prey in the north-west resulted in Cape cormorants attempting to take bait from hooks of fishing lines over an extended period, a behaviour not previously recorded. The number of Cape cormorants breeding in the south may be constrained by the absence of large islands between Dyer Island in the west and Algoa Bay in the east. If so, it may be possible to bolster the southern population through the provision of appropriate breeding habitat, such as platforms, or restricting human disturbance at suitable mainland cliff breeding sites.     

Fluid flow reconstruction in karstified Panormide platform limestones (north-central Sicily): Implications for hydrocarbon prospectivity in the Sicilian fold and thrust belt

Diagenetic analysis based on field and petrographic observations, isotope and microthermometric data was used to reconstruct the fluid flow history of the Cretaceous shallow water limestones from the Panormide platform exposed in north-central Sicily. Analysis focused on diagenetic products in cavities and dissolution enlarged fractures of the karstified limestones that occur just below a regional unconformity. The fluid flow history could be broken down into five stages that were linked to the kinematic and burial history of the region. (1) Petrography (zoned cathodoluminescence and speleothem textures) and stable isotopes (6.5 < δ¹⁸O_V-PDB < ?3.5‰ and 0 < δ¹³C_V-PDB < ?14‰) indicate that the earliest calcite phase was associated with karstification during emergence of the platform. Limestone dissolution at this stage is important with regard to possible reservoir creation in the Panormide palaeogeographic domain. (2) Fine-grained micrite sedimentation, dated as latest Cretaceous by nannopalaeontology and its ⁸⁷Sr/⁸⁶Sr isotope ratio (0.7078), marks replacement by marine fluids during subsequent submergence of the karstified platform. (3) The following calcite cement was still precipitated by marine-derived fluids (?7.0 < δ¹⁸O_V-PDB < ?5.0‰ and ?3.0 < δ¹³C_V-PDB < 0.5‰/T_m = ?2 to ?5 °C), but at increasingly higher temperatures (T_h = 60–120 °C). This has been interpreted as precipitation during Oligocene foredeep burial. (4) Hot (T_h = 130–180 °C), low saline (T_m < ?2.5 °C) fluids with increasingly higher calculated δ¹⁸O_SMOW signatures (+6 to +14‰) subsequently invaded the karst system. These fluids most likely migrated during fold and thrust belt development. The low salinity and relatively high δ¹⁸O_SMOW signatures of the fluids are interpreted to be the result of clay dewatering reactions. The presence of bitumen and associated fluorite with hydrocarbon inclusions at this stage in the paragenesis constrains the timing of oil migration in the region. (5) Finally, high saline fluids with elevated ⁸⁷Sr/⁸⁶Sr (0.7095–0.7105) signatures invaded the karst system. This last fluid flow event was possibly coeval with localized dolomitization and calcite cementation along high-angle faults of Pliocene age, as suggested by identical radiogenic signatures of these diagenetic products.     

Elemental and isotopic variations in subduction related basalts: evidence for a three component model

Subduction related basalts display wide ranges in large ion lithophile element ratios (e.g., Rb/Ba and Rb/ Sr) which are unlikely to result from mixing, but suggest a role for small degree partial melting of a relatively Rb-poor mantle wedge source. However, these variations do not correlate with other trace element criteria, such as the depletions of high field strength elements (HFSE) and light rare earth elements (LREE) relative to the LILE, which characterise subduction related magmatism. Integration of radiogenic isotope and trace element data demonstrates that the elemental enrichment cannot be simply related to two component mixtures inferred from isotopic variations. Thus a minimum of three components is required to describe the geochemistry of subduction zone basalts. Two are subduction related: high Sr/Nd material is derived from the dehydration of subducted basaltic ocean crust, and a low Sr/Nd component is thought to be from subducted terrigenous sediment. The third component is in the mantle wedge, it is usually similar to the source of MORB, particularly in its isotopic composition. However, in some cases, notably continental areas, more enriched mantle wedge material with relatively high ⁸⁷Sr/⁸⁶Sr, low ¹⁴³Nd/¹⁴⁴Nd and elevated incompatible trace element contents may be involved Mixing of these three components is capable of producing both the entire range of Sr, Nd and Pb isotope signatures observed in destructive margin basalts, and their distinctive trace element compositions. The isotope differences between Atlantic and Pacific island arc basalts are attributed to the isotope compositions of sediments in the two oceans.     

The primitive lavas of Roccamonfina volcano,Roman region,Italy: new constraints on melting processes and source mineralogy

Within a large collection of lavas from the Roccamonfina volcano are rocks which represent the most mafic samples yet recorded from Roccamonfina and which are amongst the least differentiated lavas found in the Roman co-magmatic region as a whole. These rocks extend both high-K and low-K series to more primitive values. However, petrographic and geochemical considerations rule out a primary origin, and even these mafic samples appear to record the effects of repeated episodes of fractional crystallization and hybridization. Relatively potassic samples from the low-K series are apparently transitional between low-K and high-K series, as previously delineated. However, these intermediate-K samples are not transitional in their Sr isotopic composition, suggesting that there is no continuum between low-K and high-K magma source regions. Rather, the compositional range within the low-K series appears predominantly to reflect variation in the degree of melting of a common mantle source. Analysis of the low-K series data, using an inverse method suggests a source containing amphibole and garnet, and indicates that these phases were consumed during the melting processes responsible for the low-K series magmas. The role of amphibole is further indicated by the association of low K₂O with elevated Rb concentration and, for example, higher Ce/Yb. Such variations are taken to reflect the consumption of high K/Rb amphibole during the initial phase of partial melting.     

I/I ratios in surface waters of the English Lake District

Accelerator Mass Spectrometry (AMS) was used to measure ¹²⁹I/¹²⁷I ratios in surface sea, lake, and river water samples collected in 2004 and 2005 from the English Lake District and from SW Scotland, areas which are in relatively close proximity to the Sellafield nuclear fuel reprocessing plant in NW England. The ¹²⁹I/¹²⁷I ratios in surface water collected from the shore of the Irish Sea were in the range 2.8 × 10⁻⁶ to 8.2 × 10⁻⁶. These ratios are one order of magnitude higher than that of seawater collected from the Irish Sea in 1992, correlating with the increase in ¹²⁹I content of the Sellafield liquid effluent discharge over the last decade. The ¹²⁹I/¹²⁷I ratios in lakes in the Lake District were in the range 0.7 × 10⁻⁶ to 6.4 × 10⁻⁶ and decreased exponentially as a function of distance from Sellafield. Consideration of the relative variation of stable I concentrations and ¹²⁹I/¹²⁷I ratios suggests that Sellafield gaseous discharges may be the dominant source of ¹²⁹I to the lakes.