| 1. |
- Qu, Yuangao, et al.
(författare)
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Sample-scale carbon isotopic variability and diverse biomass in the Paleoproterozoic Zaonega Formation, Russia
- 2018
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Ingår i: Precambrian Research. - 0301-9268 .- 1872-7433. ; 315, s. 222-231
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Tidskriftsartikel (refereegranskat)abstract
- The stratigraphic record of organic matter in the c. 1.97 Ga Zaonega Formation (ZF), Onega Basin, northwestern Russia, exhibits a distinct negative δ13C excursion (δ13Corg from −25 to −40‰ VPDB), which was previously interpreted either to reflect a disturbance in the global carbon cycle after the Great Oxidation Event, or to have been caused by an increase in basinal methanotrophic activity. In order to assess the nature of primary biomass and the effects of post-depositional alteration, we here report the sample-scale carbon isotopic characteristics of organic matter in two drill cores from the ZF, covering 500 m of stratigraphy, by using secondary ion mass spectrometry (SIMS). The results confirm that the organic matter has to a large extent preserved the primary isotopic signatures, whereas secondary effects are limited (<4‰). The sample-scale isotopic heterogeneity, defined as the difference between the maximum and minimum δ13C values obtained by SIMS from every individual sample, increases from typically <5‰ in the lower part of stratigraphy to systematically larger values (up to 11‰) in the upper part, which coincides with the decreasing trend of δ13Corg of bulk samples from −25 to −40‰. Samples with either relatively high (c. −25‰) or low (c. −40‰) δ13Corg values have small sample-scale isotopic heterogeneities, while samples with intermediate δ13Corg values (between −25 and −40‰) have significantly larger heterogeneities. These observations imply the co-existence of photoautotrophic and methanotrophic biomass during deposition of the upper part of the stratigraphy. Our study provides insight into the carbon isotopic characteristics of organic matter and suggests that the negative excursion of δ13Corg in the ZF is induced by a methanotrophic microbial ecosystem sustained by seepage of thermogenic methane during the deposition of the ZF and contemporaneous igneous activities.
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| 2. |
- Tillberg, Mikael, et al.
(författare)
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Fractionation of Rare Earth Elements in Greisen and Hydrothermal Veins Related to A-Type Magmatism
- 2019
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Ingår i: Geofluids. - : Hindawi Limited. - 1468-8115 .- 1468-8123. ; 2019
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Tidskriftsartikel (refereegranskat)abstract
- This study focuses on concentrations and fractionation of rare earth elements (REE) in a variety of minerals and bulk materials of hydrothermal greisen and vein mineralization in Paleoproterozoic monzodiorite to granodiorite related to the intrusion of Mesoproterozoic alkali- and fluorine-rich granite. The greisen consists of coarse-grained quartz, muscovite, and fluorite, whereas the veins mainly contain quartz, calcite, epidote, chlorite, and fluorite in order of abundance. A temporal and thus genetic link between the granite and the greisen/veins is established via high spatial resolution in situ Rb-Sr dating, supported by several other isotopic signatures (delta S-34, Sr-87/Sr-86, delta O-18, and delta C-13). Fluid-inclusion microthermometry reveals that multiple pulses of moderately to highly saline aqueous to carbonic solutions caused greisenization and vein formation at temperatures above 200-250 degrees C and up to 430 degrees C at the early hydrothermal stage in the veins. Low calculated Sigma REE concentration for bulk vein (15ppm) compared to greisen (75ppm), country rocks (173-224ppm), and the intruding granite (320ppm) points to overall low REE levels in the hydrothermal fluids emanating from the granite. This is explained by efficient REE retention in the granite via incorporation in accessory phosphates, zircon, and fluorite and unfavorable conditions for REE partitioning in fluids at the magmatic and early hydrothermal stages. A noteworthy feature is substantial heavy REE (HREE) enrichment of calcite in the vein system, in contrast to the relatively flat patterns of greisen calcite. The REE fractionation of the vein calcite is explained mainly by fractional crystallization, where the initially precipitated epidote in the veins preferentially incorporates most of the light REE (LREE) pool, leaving a residual fluid enriched in the HREE from which calcite precipitated. Fluorite occurs throughout the system and displays decreasing REE concentrations from granite towards greisen and veins and different fractionation patterns among all these three materials. Taken together, these features confirm efficient REE retention in the early stages of the system and minor control of the REE uptake by mineral-specific partitioning. REE-fractionation patterns and fluid-inclusion data suggest that chloride complexation dominated REE transport during greisenization, whereas carbonate complexation contributed to the HREE enrichment in vein calcite.
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| 3. |
- Kamenos, Nicholas A., et al.
(författare)
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Reconstructing Greenland ice sheet runoff using coralline algae
- 2012
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Ingår i: Geology. - 0091-7613 .- 1943-2682. ; 40:12, s. 1095-1098
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Tidskriftsartikel (refereegranskat)abstract
- The Greenland ice sheet (GrIS) contains the largest store of fresh water in the Northern Hemisphere, equivalent to similar to 7.4 m of eustatic sea-level rise, but its impacts on current, past, and future sea level, ocean circulation, and European climate are poorly understood. Previous estimates of GrIS melt, from 26 yr of satellite observations and temperature-driven melt models over 48 yr, show increasing melt trends. There are, however, no runoff data of comparable duration with which to validate the relationship between the spatial extent of melting and runoff or temperature-based runoff models. Further, longer runoff records are needed to extend the melt pattern of Greenland to centennial timescales, enabling recent observations and trends to be put into a better historical context. We have developed a new GrIS runoff proxy by extracting information on relative salinity changes from annual growth bands of red coralline algae. We observed significant negative relationships between historic runoff, relative salinity, and marine summer temperature in Sondre Stromfjord, Greenland. We produce the first reconstruction of runoff from a section of the GrIS that discharges into Sondre Stromfjord over several decades (1939-2002) and record a trend of increasing reconstructed runoff since the mid 1980s. In situ summer marine temperatures followed an equivalent trend. We suggest that since A. D. 1939, atmospheric temperatures have been important in forcing runoff. These results show that our technique has significant potential to enhance understanding of runoff from large ice sheets as it will enable melt reconstruction over centennial to millennial timescales.
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| 4. |
- Weihed, Pär, 1959-, et al.
(författare)
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A stable isotope study of the Palaeoproterozoic Tallberg porphyry-type deposit, northern Sweden
- 1994
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Ingår i: Mineralium Deposita. - 0026-4598 .- 1432-1866. ; 29:2, s. 128-138
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Tidskriftsartikel (refereegranskat)abstract
- The Tallberg deposit is situated in the Skellefte District in northern Sweden. It is a Palaeoproterozoic equivalent of Phanerozoic poryphyry-type deposits. The mineralization is situated within the Jörn granitoid complex and is associated with intrusive quartz-feldspar porphyries. The granitoids are coeval with mainly felsic volcanic rocks hosting several massive sulphide deposits. The alteration is generally of a mixed phyllic-propylitic type, but areas or zones associated with high gold grades exhibit phyllic alteration. Ore minerals are pyrite, chalcopyrite, sphalerite, magnetite, and trace amounts of molybdenite. In this stable isotope study, quartz, sericite, and chlorite from the alteration zones were sampled. The magmatic quartz has a 18O composition of + 6.2 to +6.7 whereas the quartz in the hydrothermal alteration zones have values ranging from +7.5 to +10.6. The calculated temperatures for this fractionation range from 430° to 520°C. The sericites have 18O ranging from +4.6 to +8.2 (average +6.6) and D -31 to -54 (average -41). Chlorites range from 18O +4.2 to +7.7 and D from -34 to -44. The range of 34S of 11 pyrite samples is +3.8 to +5.5 with an average of +4.6 ± 0.5, suggesting a relatively homogeneous sulphur source, probably of magmatic origin. Modelling waters in equilibrium with the minerals indicates early magmatic fluids with 18O of 6.5. This fluid mixed with a low 18O and high D fluid, which is tentatively identified as seawater. The 18O signature of sericite and chlorite also indicates significant water-rock exchange, explaining the positive 18O values for the waters in equilibrium with the hydrated minerals.
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