Arsenic and antimony contamination of waters,stream sediments and soils in the vicinity of abandoned antimony mines in the Western Carpathians,Slovakia

Environmental contamination with As and Sb caused by past mining activities at Sb mines is a significant problem in Slovakia. This study is focused on the environmental effects of the 5 abandoned Sb mines on water, stream sediment and soil since the mines are situated in the close vicinity of residential areas. Samples of mine wastes, various types of waters, stream sediments, soils, and leachates of the mine wastes, stream sediments and selected soils were analyzed for As and Sb to evaluate their geochemical dispersion from the mines. Mine wastes collected at the mine sites contained up to 5166 mg/kg As and 9861 mg/kg Sb. Arsenic in mine wastes was associated mostly with Fe oxides, whereas Sb was present frequently in the form of individual Sb, Sb(Fe) and Fe(Sb) oxides. Waters of different types such as groundwater, surface waters and mine waters, all contained elevated concentrations of As and Sb, reaching up to 2150 μg/L As and 9300 μg/L Sb, and had circum-neutral pH values because of the buffering capacity of abundant Ca- and Mg-carbonates. The concentrations of Sb in several household wells are a cause for concern, exceeding the Sb drinking water limit of 5 μg/L by as much as 25 times. Some attenuation of the As and Sb concentrations in mine and impoundment waters was expected because of the deposition of metalloids onto hydrous ferric oxides built up below adit entrances and impoundment discharges. These HFOs contained >20 wt.% As and 1.5 wt.% Sb. Stream sediments and soils have also been contaminated by As and Sb with the peak concentrations generally found near open adits and mine wastes. In addition to the discharged waters from open adits, the significant source of As and Sb contamination are waste-rock dumps and tailings impoundments. Leachates from mine wastes contained as much as 8400 μg/L As and 4060 μg/L Sb, suggesting that the mine wastes would have a great potential to contaminate the downstream environment. Moreover, the results of water leaching tests showed that Sb was released from the solids more efficiently than As under oxidizing conditions. This might partly explain the predominance of Sb over As in most water samples.     

Sequestration mechanisms and anthropogenic inputs of rhenium in sediments from Eastern Canada lakes

The concentrations of Re, as well as those of several other geochemical variables, were measured in dated sediment cores and in porewater samples from four lacustrine basins in Eastern Canada: one, perennially oxic, located 40 km from Québec City and three, seasonally anoxic, located within 25 km of non-ferrous metal smelters. The drainage basins of these lakes are uninhabited and have not been affected by human activity or wildfires. All of the depth profiles of dissolved Re indicate: higher Re concentrations in the water overlying the sediment than in the porewater; diffusion of Re across the sediment-water interface; a progressive decrease in porewater Re concentrations to reach minimum values of ∼0.5 pM within a 10-cm sediment depth interval. Modeling of these Re porewater profiles with a one-dimensional transport-reaction equation indicates that Re is removed from porewater within this depth interval. Based on thermodynamic predictions of Re speciation and of saturation states and on comparison of these predictions with sulfide porewater profiles, we infer that Re is removed from porewater by precipitation of rheniite (ReS_2(s)). The rate constant for the formation of ReS_2(s) in sediments is estimated from the modeling exercise to be 0.51 ± 0.64 × 10⁻²¹ mol cm⁻³ s⁻¹. Accumulation of sedimentary Re shows a strong authigenic component, as in anoxic marine sediments. Sharp increases in solid-phase Re during the last century are attributed to atmospheric deposition of anthropogenic Re deriving from coal burning and nearby smelter emissions.     

Arsenic in sediments, groundwater, and streamwater of a glauconitic Coastal Plain terrain, New Jersey, USA—Chemical “fingerprints” for geogenic and anthropogenic sources

Glauconite-bearing deposits are found worldwide, but As levels have been determined for relatively few. The As content of glauconites in sediments of the Inner Coastal Plain of New Jersey can exceed 100 mg/kg, and total As concentrations (up to 5.95 μg/L) found historically and recently in streamwaters exceed the State standard. In a major watershed of the Inner Coastal Plain, chemical “fingerprints” were developed for streambed sediments and groundwater to identify contributions of As to the watershed from geologic and anthropogenic sources. The fingerprint for streambed sediments, which included Be, Cr, Fe and V, indicated that As was predominantly of geologic origin. High concentrations of dissolved organic C, nutrients (and Cl⁻) in shallow groundwater indicated anthropogenic inputs that provided an environment where microbial activity released As from minerals to groundwater discharging to the stream. Particulates in streamwater during high flow constituted most of the As load; the chemical patterns for these particulates resembled the geologic fingerprint of the streambed sediments. The As/Cr ratio of these suspended particles likely indicates they derived not only from runoff, but from groundwater inputs, because As contributed by groundwater is sequestered on streambed sediments. Agricultural inputs of As were not clearly identified, although chemical characteristics of some sediments indicated vehicle-related inputs of metals. Sediment sampling during dry and wet years showed that, under differing hydrologic conditions, local anthropogenic fingerprints could be obscured but the geologic fingerprint, indicating glauconitic sediments as an As source, was robust.     

Arsenic and metal contamination of water resources from mining wastes in Korea

 Water resources near a gold-mine waste site were studied for the distribution and contents of contaminants, and their behavior in the surface and groundwater systems. Arsenic, cadmium, and manganese were identified with levels exceeding the drinking water guidelines of WHO (World Health Organization), and their distribution depended upon the differences in source materials and in spatial pH variations. Originating from arsenopyrite, concentrations of dissolved arsenic were controlled by sorption with amorphous iron (Fe(OH)₃) and carbonate minerals. Cadmium and manganese were derived from the mineral phase including sphalerite (ZnS), otavite (CdCO₃), and rhodochrosite (MnCO₃); their concentrations in water resources were limited by the solubility of mineral phases. All of these processes are significantly pH-dependent, implying that a small decline in pH could result in a drastic increase in contaminant concentrations and become a pollution threat to the water resources of the Gubong area. Received: 13 December 1999 · Accepted: 21 March 2000     

Geochemical and anthropogenic enrichments of Mo in sediments from perennially oxic and seasonally anoxic lakes in Eastern Canada

We measured the vertical distributions of Mo, Fe, Mn, sulfide, sulfate, organic carbon, major ions, and pH in sediment porewater from one perennially oxic and three seasonally anoxic lacustrine basins in Eastern Canada, as well as those of Mo, acid volatile sulfide, Fe, Mn, Al, organic C, ²¹⁰Pb and ¹³⁷Cs in sediment cores from the same sites. The only input of anthropogenic Mo to these lakes comes from atmospheric deposition.The relatively monotonous distribution of Mo in the porewater of three seasonally anoxic basins suggests that Mo is not redistributed in the sedimentary column during periods of anoxia. In contrast, porewater Mo profiles obtained at three sampling dates in a perennially oxic basin display sharp Mo peaks below the sediment-water interface, indicating redistribution subsequent to deposition. Modeling of these latter porewater Mo profiles with a diagenetic reaction-transport equation coupled to comparisons among the various porewater and solid phase profiles reveal that Mo is released at 1-2 cm depth as a consequence of the reductive dissolution of Fe oxyhydroxides and scavenged both at the vicinity of the sediment-water interface, by re-adsorption onto authigenic Fe oxyhydroxides, and deeper in the sediments where dissolved sulfide concentrations are higher. The estimated rate constant for the adsorption of Mo onto Fe oxyhydroxides is 36 ± 45 cm³ mol⁻¹ s⁻¹.Diagenetic modeling indicates that authigenic Mo in sediments of the perennially oxic basin represents about one-third of the total solid phase Mo in the first cm below the sediment-water interface and only one tenth below this horizon. If we assume that no authigenic Mo is accumulated in the seasonally anoxic lake sediments we conclude that the sediment Mo concentrations, which are up to 3-16 times higher than the average lithogenic composition, depending on the lake, are mainly due to atmospheric deposition of anthropogenic Mo and not to the formation of authigenic Mo phases. Reconstructed historical records of the atmospheric Mo deposition indicate maximum values in the 1970s and 1980s and significant decreases since then. Emissions to the atmosphere associated with the smelting of non-ferrous ores and coal combustion appear to be the most important sources of anthropogenic Mo.     

Detection of petroleum contamination in river sediments from Quebec City region using GC–IRMS

Isotopic analysis by compound specific gas chromatography–isotope ratio mass spectrometry (GC–IRMS) is used to detect and characterize petroleum pollution in surficial sediments along the St Lawrence River, near Quebec City. Unusually mature n-alkane distributions have been found in some recent intertidal sediments in the region. GC–IRMS results suggest that the n-alkanes are not derived from indigenous organic sources because they carry δ¹³C values between −30.0 and −27.0‰, as well as very small isotopic differences between odd and even numbered n-alkanes, which are both typically associated with petroleum products. Comparison of these sediments with bunker fuel, an oil used in the shipping industry, has shown a close isotopic correlation in some sites, which is further supported by biomarkers. Overall, the contamination has been dispersed along the river but is generally localized around the industrial region where hydrocarbon transfer from shore storage to ships takes place. This study illustrates how GC–IRMS can be used effectively in the detection and characterization of petroleum pollutants in sediments.     

Arsenic in framboidal pyrite from recent sediments of a shallow water lagoon of the Baltic Sea

Arsenic is a redox‐sensitive element of environmental relevance and often enriched in iron sulphides. Because sediments from the Achterwasser lagoon, a part of the estuarine system of the river Oder, south‐west Baltic Sea, show unexpectedly high pyrite concentrations of up to 7·5 wt% they were used to investigate the influence of authigenic pyrite on the mobility and burial of As in the coastal environment. Micro‐X‐ray‐fluorescence measurements of 106 micrometre‐sized pyrite framboids from the anoxic sediments show highly variable As concentrations ranging from 6 to 1142 μg g^?1. Even within a 1 cm thick layer, the As concentration of different framboids varies greatly and no clear depth trend is visible throughout the 50 cm long sediment core. Pyrite can account for 9 to 55% (average 22%) of the total As budget of the sediments and the degree of trace metalloid pyritization for As ranges from 26 to 61%, indicating that authigenic pyrite formation is an important process in the geochemical cycling of As in coastal sediments. High‐resolution micro‐X‐ray fluorescence mapping of single pyrite grains shows that As is distributed inhomogeneously within larger framboids, suggesting changing pore water composition during pyrite growth. X‐ray absorption near edge structure spectra indicate that As is usually present as As(‐I) substituting S in the pyrite lattice. However, in samples close to the sediment/water interface a considerable part of As is in higher valence states (+III/+V). This can be explained by frequent re‐suspension of the surficial sediments to the oxic water column due to wave action and subsequent re‐deposition, leading to the adsorption of As oxyanions onto pyrite. Although reduced As(‐I) becomes more important in the deeper samples, reflecting decreasing redox potential and a longer time since deposition, the occurrence of oxidized As species (AsIII/AsV) in pyrite in the anoxic part of the sediment suggests formation under dysoxic conditions.     

Microsedimentology of ice stream tills from the Eastern Alps,Austria – a new perspective on till microstructures

This study of tills from the Eastern Alps, Austria, illustrates the insights obtained using microsedimentology on subglacial tills in the context of palaeogeographical reconstructions of glacier advances. Investigations of several sites with tills derived from both local glaciers and the ice‐sheet streaming of the Inn Glacier during the Last Glacial Maximum and its termination reveal a detailed picture of subglacial sedimentology that provides evidence of soft sediment subglacial deformation under polythermal conditions. All the tills exhibit microstructures that are proxy evidence of significant changes in till rheology. The tills originate from multiple sources, incorporating older tills and other deposits picked up by the subglacial deformation within a polythermal but dominantly warm temperate subglacial thermal regime. The analyses of till microstructures reveal a direct relationship between basal ice strain conditions and their development. A hypothesis is derived, from the various microstructures observed in these Austrian tills formed under soft sediment deforming basal ice conditions, that suggests that with basal thermal changes and fluctuations in clay content, pore‐water content and pressure, microstructures form in a non‐random manner. It is postulated that in clay‐deficient sediments, edge‐to‐edge events are most likely to occur first; and where clay content increases, grain stacks, rotation structures, deformation bands and, finally, shear zones are likely to evolve in an approximate sequential manner. After repeated transport, emplacement, reworking and, probably, further shearing and deformation events, an emplaced ‘till’, as observed in these Austrian tills, will form that carries most, if not all of these microstructures, in varying percentages. Finally, the impact of the Inn Glacier Ice Stream on these tills is not easily detected and/or differentiated, but indications of high pore water and probable dilatant events leading to reductions in the number of edge‐to‐edge events point to the impact of fast or thick ice upon these subglacial tills.     

Comment on “First Record of Hindeodus–Isarcicella Population in Lower Triassic of Slovenia” by Tea Kolar-Jurkov?ek and Bogdan Jurkov?ek in Palaeogeography, Palaeoclimatology, Palaeoecology, 252: 72–81

Some conodonts described by Tea Kolar-Jurkovsek and Bogdan Jurkovsek (2007) from the Permian-Triassic boundary section in the ?iri area of western Slovenia are revised in this paper. One specimen that they assigned to Hindeodus parvus is tentatively regarded as Hindeodus cf. scalaris Wu 2005. Two specimens that they assigned to Isarcicella sp. A is changed to Hindeodus parvus. One specimen that they described as Isarcicella lobata Perri and Farabegoli is changed to Hindeodus crenatus Wu (2006). One specimen that they assigned to Isarcicella turgida (Kozur, Mostler and Rahimi-Yazd) is changed to Hindeodus cf. parvus. Since these revisions, the three conodont zones that they defined have been correspondingly revised. Their first zone may belong to Hindeodus parvus zone, but it is not certain. Their second zone is changed to the Hindeodus parvus zone, and their third one remains as is.     

Hydrocarbons in the water and bottom sediments of a region with continuous petroleum contamination

The abundances and compositions of aliphatic hydrocarbons (AHC) and polyaromatic hydrocarbons (PAH) were investigated in the water and bottom sediments of the southwestern Amur Bay in the Sea of Japan. The water contained from 0 to 129 μg/1AHC (averaging 42.2 μg/l) and from 5 to 85 ng/l PAH (averaging 18 ng/l). The bottom sediments contained 168–2098 μg/g AHC and 7.2–1100 ng/g dry mass PAH. It was shown that the input of anthropogenic HC is better recorded by molecular markers than the distribution of AHC and PAH concentrations. The discovery of elevated HC concentrations in the bottom water layer suggests that the bottom sediments induced secondary contamination of the water body.     

The spectacular fossils of the ‘water margin’: the Cambrian biota of Chengjiang,Yunnan, China

Shi Nai'an's fourteenth century Chinese epic ‘Water Margin’ tells of the release of 36 heavenly spirits and 72 baleful stars from their captivity beneath a tablet of stone at Mount Longhu in Jiangxi Province. They are reincarnated as the 108 heroes of the Liangshan marsh in Shandong Province, who rise against an unjust world. The virtuous exploits of the ‘108’ were brought to life through the cathode‐ray screens of 1970s television sets, as the TV series The Water Margin introduced heroes like Lin Chong battling his evil nemesis Gao Qiu. Far to the west of Jiangxi Province and several hundred years after the Water Margin during the summer of 1984, a young scientist from Nanjing was working amongst the hills and lakes of southern Yunnan Province. He too overturned a stone slab, releasing from their half‐billion year captivity a cornucopia of new Chinese legends. His name was Xianguang Hou and he had made one of the most momentous fossil discoveries in history, uncovering the exceptionally preserved marine fossils of the Chengjiang biota from the ancient water margin of Cambrian seas.     

The origin of chloritoid – 3‐mica pseudomorph growth in staurolite–muscovite schist,Bangriposi (Eastern India)

At Bangriposi, variable stages in replacement of staurolite by chloritoid – Na–K–Ca mica shimmer aggregates in muscovite schists provides insight into the complex interplay between fluid flow, mass transfer, and dissolution–precipitation during pseudomorph growth. Idioblastic chloritoid growing into mica caps without causing visible deformation, and monomineralic chloritoid veins (up to 300 μm wide) within shimmer aggregates replacing staurolite attest to chloritoid nucleation in fluid‐filled conduits along staurolite grain boundaries and crystallographic planes. The growth of shimmer aggregates initiated along staurolite margins, and advanced inwards into decomposing staurolite along networks of crystallographically controlled fluid‐filled conduits. Coalescence among alteration zones adjacent to channel fills led to dismemberment and the eventual demise of staurolite. Mass balance calculation within a volume‐fixed, silica‐conserved reference frame indicate the shimmer aggregates grew via precipitation from fluids in response to mass transport that led to the addition of H₂O, K₂O, Na₂O and CaO in the reaction zone, and Al₂O₃ was transported outward from the inward‐retreating margin of decomposing staurolite. This aided precipitation of chloritoid in veins and in the outer collars, and as disseminated grains in the shimmer aggregates at mid‐crustal condition (~520 ± 20 °C, 5.5 ± 2.0 kbar). Computation using one‐dimensional transport equation suggests that staurolite decomposition involved advection dominating over diffusive transport; the permeation of externally derived H₂O caused flattening of chemical potential gradients in H₂O and aqueous species, for example, and , computed using the Gibbs method. This suggests that staurolite decomposition was promoted by the infiltration of a large volume of H₂O that flattened existing chemical potential gradients. In the initial stages of replacement, chloritoid super‐saturation in fluid caused preferential nucleation and growth of chloritoid at staurolite grain boundaries and in crystallographic planes. As reaction progressed, further chloritoid nucleation was halted, but chloritoid continued to grow as the 3‐mica aggregates continued to replace the remaining staurolite in situ, while the chloritoid‐compatible elements were transported in the water‐rich phase facilitating continued growth of the existing chloritoid grains.     

Organic contamination identification in sediments from a Mediterranean coastal ecosystem: The case of the Nador lagoon (Eastern Morocco)

The Nador lagoon ecosystem (North-East of Morocco) displays a major socioeconomic interest. In fact, it is essential to evaluate consequences of anthropogenic activities in the lagoon especially by organic matter studies (nature and distribution) in the sedimentary compartment. Surface sediments show variable rates in total organic carbon and in sulfur, high in some cases (7.5 and 1.8% respectively). These high contents are recorded in the center of the lagoon. Their distributions are controlled by the hydrodynamism and the anthropogenic degree. The molecular biomarkers analyses and especially n-alkanes distribution reveal: a zone of marine influence; and a zone of continental influence. The occurrence of pentacyclic triterpanes with a typical distribution of a thermally mature organic matter reveals a contamination due to petroleum products in the entire lagoon except for the center. Coprostanol occurrence near cities indicates wastewater effluents inputs and reducing conditions underlined by high values of stanols/sterol ratios. Thus, the organic contamination (petroleum by-products and wastewater effluents) occurs in the vicinity of the cities whereas the littoral edge and center remain weakly affected by these contaminations.     

Natural and anthropogenic influences on the geochemistry of Quaternary lake sediments from Holzmaar, Germany

 The accumulation of heavy metals and trace elements has been investigated in a well laminated sequence of Holocene and late Pleistocene lake sediments composed of diatomaceous gyttja, tuff and silt and clay sediments. Varve chronology of the annually deposited gyttja yielded a continuous high-resolution time sequence and allowed the absolute age dating of the sediment. Fluxes of elements remained largely uniform from the late Pleistocene into the Holocene (12 867–2 364 VT years ago; VT: varve time, years before 1950). Higher trace element and heavy metal fluxes occur from 2 322 to 862 VT years ago and reached their maxima in the uppermost sediments (<845 VT years ago). These increasing element fluxes correlate with increasing inputs of clastic material. The changing accumulation rates are the result of elevated soil erosion in the lake catchment caused by human settlement, deforestation and agricultural activities. Thus disturbances of the natural geochemical cycles of the Holzmaar region have occurred since the beginning of the Iron Age and especially since the beginning of the Middle Ages. Received: 29 May 1996 · Accepted: 19 August 1996     

Heavy metals contamination in water and sediments of an urban river in a developing country

Water and sediment samples were collected from 20 location of the Buriganga river of Bangladesh during Summer and Winter 2009 to determine the spatial distribution, seasonal and temporal variation of different heavy metal contents. Sequential extraction procedure was employed in sediment samples for the geochemical partitioning of the metals. Total trace metal content in water and sediment samples were analyzed and compared with different standard and reference values. Concentration of total chromium, lead, cadmium, zinc, copper, nickel, cobalt and arsenic in water samples were greatly exceeded the toxicity reference values in both season. Concentration of chromium, lead, copper and nickel in sediment samples were mostly higher than that of severe effect level values, at which the sediment is considered heavily polluted. On average 72 % chromium, 92 % lead, 88 % zinc, 73 % copper, 63 % nickel and 68 % of total cobalt were associated with the first three labile sequential extraction phases, which portion is readily bioavailable and might be associated with frequent negative biological effects. Enrichment factor values demonstrated that the lead, cadmium, zinc, chromium and copper in most of the sediment samples were enriched sever to very severely. The pollution load index value for the total area was as high as 21.1 in Summer and 24.6 in Winter season; while values above one indicates progressive deterioration of the sites and estuarine quality. The extent of heavy metals pollution in the Buriganga river system implies that the condition is much frightening and may severely affect the aquatic ecology of the river.     

Melonite group minerals and other tellurides from three Cu–Ni–PGE prospects, Eastern Desert, Egypt

Melonite group minerals and other tellurides are described from three Cu–Ni–PGE prospects in the Eastern Desert of Egypt: Gabbro Akarem, Genina Gharbia and Abu Swayel. The prospects are hosted in late Precambrian mafic–ultramafic rocks and have different geologic histories. The Gabbro Akarem prospect is hosted in dunite pipes where net-textured and massive sulfides are associated with spinel and Cr-magnetite. Michenerite, merenskyite, Pd–Bi melonite and hessite occur mainly as inclusions in sulfides. Typical magmatic textures indicate a limited role of late- and post-magmatic hydrothermal processes. At Genina Gharbia, ore forms either disseminations in peridotite or massive patches in hornblende-gabbro in the vicinity of metasedimentary rocks. Actinolitic hornblende, epidote, chlorite and quartz are common secondary silicates. Sulfide textures and host rock petrography suggest a prolonged late-magmatic hydrothermal event. Michenerite, merenskyite, Pd–Bi melonite, altaite, hessite, tsumoite, sylvanite and native Te are mainly present in secondary silicates. The Abu Swayel prospect occurs in conformable, lens-like mafic–ultramafic rocks in metasedimentary rocks and along syn-metamorphic shear zone. The sulfide ore and host rocks are metamorphosed (amphibolite facies; 550 to 650 °C, 4 to 5 kbar) and syn-metamorphically sheared. Melonite group minerals are represented by merenskyite and Pd–Bi melonite. Other tellurides comprise hessite, altaite and joséite-B. Melonite group minerals and tellurides occur as inclusions in mobilized sulfides and along cracks in metamorphic garnet and plagioclase.The different geological history of the three prospects permits an examination of the role played by magmatic, late-magmatic and metamorphic processes on the mineralogy of melonite group minerals and diversity of tellurides. The contents of PGE and Te in the ore and temperature of crystallization control the mineralogy and compositional trends of the melonite group minerals. Crystallization of the melonite group minerals over a wide range of temperatures in a Te-rich environment enhances the elemental substitutions. Merenskyite dominates the mineralogy of the group at low Te activity, while Pd–Bi melonite is the common phase at high Te activity.     

Vented sediments and tsunami deposits in the Puget Lowland,Washington – differentiating sedimentary processes

The sandy deposits produced by tsunamis and liquefaction share many sedimentary features, and distinctions between the two are important in seismically active coastal zones. Both types of deposits are present in the wetlands bordering Puget Sound, where one or more earthquakes about 1100 years ago caused both tsunami flooding and sediment venting. This co‐occurrence allows an examination of the resulting deposits and a comparison with tsunami and liquefaction features of modern events. Vented sediments occur at four of five wetland field localities and tsunami deposits at two. In comparison with tsunami deposits, vented sediments in this study and from other studies tend to be thicker (although they can be thin). Vented sediments also have more variable thickness at both outcrop and map scale, are associated with injected dykes and contain clasts derived from underlying deposits. Further, vented sediments tend to contain a greater variety of sedimentary structures, and these structures vary laterally over metres. Tsunami deposits compared with vented sediments are commonly thinner, fine and thin landward more consistently, have more uniform thickness on outcrop and map scales, and have the potential of containing coarser clasts, up to boulders. For both tsunami deposits and vented sediments, the availability and grain size of source material condition the characteristics of the deposit. In the cases presented in this paper, both foraminifera and diatom assemblages within tsunami deposits and vented sediments consisted of brackish and marine species, and no distinction between processes could be made based on microfossils. In summary, this study indicates a need for more careful analysis and mapping of coastal sediments associated with earthquakes to avoid misidentification of processes and misevaluation of hazards.     

Free and bound lipids in recent (1835–1987) sediments from Santa Barbara Basin

In order to study the first steps of incorporation of lipids in recent organic-rich sediments into free and bound fractions, we have selected the Santa Barbara Basin, off California. This basin with a maximum of 590 m water depth is characterized by high phytoplankton production in surface waters and a low oxygen content in bottom waters. Sediments show the following features: high sedimentation rate ≈ 4 mm/yr, no bioturbation, and development of a bacterial mat community at the surface with predominance of sulphur-oxidizing bacteria trapping particles, thus preventing re-distribution of sediment, which permit a unique observations of organic sedimentation on a new few years basis.A sediment core has been divided into 2 cm thick slices corresponding to a time resolution of ≈5 years, from 1835 up to 1987. Samples have been analyzed using a multi-parameter approach, such as for plankton species identification, carbon stable isotope ratios and, as reported here, for lipid organic tracers. Organic tracers have been analyzed in the sterol and fatty series for both free and bound compounds by gas chromatography and gas chromatography/mass spectrometry.The incorporation processes of sterols with depth appear different for free and bound compounds. Total free sterol concentrations show high values in surface sediments (≈ 100 μg/g dry sediment), rapidly decrease up to ≈ 10 cm depth and remain at a constant value of 30–40 μg/g. Total bound sterol concentrations show low values in surface sediment (13.6 μg/g), and vary irregularly with depth up to a value of 55 μg/g at 7.3 m, and then remain constant at 25–26 μg/g.Profiles of evolution with depth of free C₂₇, C₂₈ sterols show a regular decrease, whereas C₂₉ sterols show an irregular decrease with anomalies at 7.3 cm (approximately age: 1977–1978) and at 14.1 cm (1962–1964). Profiles of bound compounds are rather different, very regular for C₂₈ sterols, irregular with oscillations for C₂₇ and C₂₉ sterols at 7.3, 12.2 and 18.0 cm (1954–1956), suggesting a different mode of incorporation and probably different inputs for C₂₇, C₂₉ and C₂₈ sterols.The study of the kinetics of degradation of sterols between surface (1987) and 10.5 cm (1968–1972) shows that C₂₇ compounds are degraded at a slight higher rate (0.53 μg/μg of initial C₂₇ concentration/ year) than are C₂₈ and C₂₉ compounds (0.047 μg/μg of initial concentration/year). An intermediate value is found for brassicasterol: 0.049 μg/μg/year.     

Crustal contamination of mafic magmas: evidence from a petrological, geochemical and Sr–Nd–Os–O isotopic study of the Proterozoic Isortoq dike swarm, South Greenland

The mid-Proterozoic Isortoq dike swarm in the Gardar Province, South Greenland, comprises a variety of alkaline rocks ranging from gabbroic to syenitic in composition. Major magmatic mineral phases are olivine, clinopyroxene, Fe–Ti oxides, amphibole, plagioclase and alkali feldspar. Quartz occurs in some samples as a late magmatic phase. Liquidus temperatures of olivine-bearing samples range between 1120 and 1145 °C and solidus temperatures are 850–930 °C. Calculated silica activities are highly variable between 0.53 and unity. Oxygen fugacities vary from −3 to +1 log units relative to the fayalite–magnetite–quartz buffer.

The rocks have MgO contents <6 wt.% with Mg# between 53 and 17. Primitive mantle-normalized trace element patterns show a relative enrichment of LIL elements with Ba peaks and Nb troughs. Clinopyroxenes show a general enrichment in REE relative to chondritic values with variable slightly positive to prominent negative Eu anomalies. Two of the dikes were dated with Sm–Nd three-point isochrons at 1190±44 and 1187±87 Ma, respectively. Initial ⁸⁷Sr/⁸⁶Sr ratios of mafic mineral separates range from 0.70289 to 0.70432 and initial _Nd values vary from +0.3 to −10.7. Whole-rock initial ¹⁸⁷Os/¹⁸⁸Os ratios are highly variable including very radiogenic values of up to 7.967. δ¹⁸O_v-smow values of separated clinopyroxene and amphibole range from +5.2‰ to +6.2‰ and fall within the range of typical mantle-derived rocks, although mixing with a lower crustal component is permitted by the data. Using energy-constrained assimilation-fractional crystallization (EC-AFC) modeling equations, the Sr–Nd isotope data of the more radiogenic samples can successfully be modeled by addition of up to 10% lower crustal granulite-facies Archean gneisses as contaminants. The Os isotopic data also suggest the involvement of old radiogenic crust. In accordance with seismic data, we conclude that a wedge of Archean crust extends from West Greenland further to the south below the present erosion level.