scholarly journals Pyrite sulfur isotopes reveal glacial−interglacial environmental changes

2017 ◽  
Vol 114 (23) ◽  
pp. 5941-5945 ◽  
Author(s):  
Virgil Pasquier ◽  
Pierre Sansjofre ◽  
Marina Rabineau ◽  
Sidonie Revillon ◽  
Jennifer Houghton ◽  
...  
Keyword(s):  
Isotopic Composition ◽  
Sea Level ◽  
Environmental Changes ◽  
Sulfur Isotopes ◽  
Atmospheric Oxygen ◽  
Sulfur Cycle ◽  
Sulfur Isotopic Composition ◽  
Temperature Changes ◽  
Depositional Controls ◽  
Surface Redox

The sulfur biogeochemical cycle plays a key role in regulating Earth’s surface redox through diverse abiotic and biological reactions that have distinctive stable isotopic fractionations. As such, variations in the sulfur isotopic composition (δ34S) of sedimentary sulfate and sulfide phases over Earth history can be used to infer substantive changes to the Earth’s surface environment, including the rise of atmospheric oxygen. Such inferences assume that individual δ34S records reflect temporal changes in the global sulfur cycle; this assumption may be well grounded for sulfate-bearing minerals but is less well established for pyrite-based records. Here, we investigate alternative controls on the sedimentary sulfur isotopic composition of marine pyrite by examining a 300-m drill core of Mediterranean sediments deposited over the past 500,000 y and spanning the last five glacial−interglacial periods. Because this interval is far shorter than the residence time of marine sulfate, any change in the sulfur isotopic record preserved in pyrite (δ34Spyr) necessarily corresponds to local environmental changes. The stratigraphic variations (>76‰) in the isotopic data reported here are among the largest ever observed in pyrite, and are in phase with glacial−interglacial sea level and temperature changes. In this case, the dominant control appears to be glacial−interglacial variations in sedimentation rates. These results suggest that there exist important but previously overlooked depositional controls on sedimentary sulfur isotope records, especially associated with intervals of substantial sea level change. This work provides an important perspective on the origin of variability in such records and suggests meaningful paleoenvironmental information can be derived from pyrite δ34S records.

Biogeochemical disruptions across the Cretaceous-Paleogene boundary : insights from sulfur isotopes

2021 ◽  
Author(s):  
Arbia Jouini
Keyword(s):  
Mass Extinction ◽  
Environmental Changes ◽  
Sea Water ◽  
Sulfur Isotopes ◽  
Deep Understanding ◽  
Sulfur Cycle ◽  
Mass Extinctions ◽  
Deccan Volcanism ◽  
Organic Carbon Burial ◽  
Early Paleocene

<p><strong>Biogeochemical disruptions across the Cretaceous-Paleogene boundary : insights from sulfur isotopes</strong></p><p> </p><p>Arbia JOUINI<sup>1*</sup>, Guillaume PARIS<sup>1</sup>, Guillaume CARO<sup>1</sup>, Annachiara BARTOLINI<sup>2</sup></p><p><sup>1 </sup>Centre de Recherches Pétrographiques et Géochimiques, CRPG-CNRS, UMR7358, ,15 rue Notre Dame des Pauvres, BP20, 54501Vandoeuvre-lès-Nancy, France, email:[email protected]</p><p><sup>2</sup> Muséum National D’Histoire Naturelle, Département Origines & Evolution, CR2P MNHN, CNRS, Sorbonne Université, 8 rue Buffon CP38, 75005 Paris, France</p><p> </p><p>The Cretaceous–Paleogene (KPg) mass extinction event 66 million years ago witnessed one of the ‘Big Five’ mass extinctions of the Phanerozoic. Two major catastrophic events, the Chicxulub asteroid impact and the Deccan trap eruptions, were involved in complex climatic and environmental changes that culminated in the mass extinction including oceanic biogenic carbonate crisis, sea water chemistry and ocean oxygen level changes. Deep understanding of the coeval sulfur biogeochemical cycle may help to better constrain and quantify these parameters.</p><p>Here we present the first stratigraphic high resolution isotopic compositions of carbonate associated sulfate (CAS) based on monospecific planktic and benthic foraminifers' samples during the Maastrichtian-Danian transition from IODP pacific site 1209C. Primary δ34SCAS data suggests that there was a major perturbation of sulfur cycle around the KPg transition with rapid fluctuations (100-200kyr) of about 2-4‰ (±0.54‰, 2SD) during the late Maastrichtian followed by a negative excursion in δ34SCAS of 2-3‰ during the early Paleocene.</p><p>An increase in oxygen levels associated with a decline in organic carbon burial, related to a collapse in primary productivity, may have led to the early Paleocene δ34SCAS negative shift via a significant drop in microbial sulfate reduction. Alternatively, Deccan volcanism could also have played a role and impacted the sulfur cycle via direct input of isotopically light sulfur to the ocean. A revised correlation between δ34SCAS data reported in this study and a precise dating of the Deccan volcanism phases would allow us to explore this hypothesis.</p><p>Keywords : KPg boundary, Sulphur cycle, cycle du calcium, Planktic and benthic foraminifera</p><p> </p>

scholarly journals Multiple Sulfur Isotope Records of the 3.22 Ga Moodies Group, Barberton Greenstone Belt

Geosciences ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 145 ◽  
Author(s):  
Masafumi Saitoh ◽  
Sami Nabhan ◽  
Christophe Thomazo ◽  
Nicolas Olivier ◽  
Jean-François Moyen ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Isotopic Composition ◽  
Greenstone Belt ◽  
Sulfur Isotope ◽  
Secondary Ion Mass Spectrometry ◽  
Sulfur Isotopes ◽  
Volcanic Rocks ◽  
Isotope Ratio Mass Spectrometry ◽  
Sulfur Isotopic Composition ◽  
Barberton Greenstone Belt

The Moodies Group, the uppermost unit in the Barberton Greenstone Belt (BGB) in South Africa, is a ~3.7-km-thick coarse clastic succession accumulated on terrestrial-to-shallow marine settings at around 3.22 Ga. The multiple sulfur isotopic composition of pyrite of Moodies intervals was newly obtained to examine the influence of these depositional settings on the sulfur isotope record. Conglomerate and sandstone rocks were collected from three synclines north of the Inyoka Fault of the central BGB, namely, the Eureka, Dycedale, and Saddleback synclines. The sulfur isotopic composition of pyrite was analyzed by Secondary Ion Mass Spectrometry (SIMS) for 6 samples from the three synclines and by Isotope Ratio Mass Spectrometry (IR-MS) for 17 samples from a stratigraphic section in the Saddleback Syncline. The present results show a signal of mass-independent fractionation of sulfur isotopes (S-MIF), although t-tests statistically demonstrated that the Moodies S-MIF signals (mostly 0‰ < ∆33S < +0.5‰) are significantly small compared to the signal of the older Paleoarchean (3.6–3.2 Ga) records. These peculiar signatures might be related to initial deposition of detrital pyrite of juvenile origin from the surrounding intrusive (tonalite–trondhjemite–granodiorite; TTG) and felsic volcanic rocks, and/or to secondary addition of hydrothermal sulfur during late metasomatism. Moreover, fast accumulation (~0.1–1 mm/year) of the Moodies sediments might have led to a reduced accumulation of sulfur derived from an atmospheric source during their deposition. As a result, the sulfur isotopic composition of the sediments may have become susceptible to the secondary addition of metasomatic sulfur on a mass balance point of view. The sulfur isotopic composition of Moodies pyrite is similar to the composition of sulfides from nearby gold mines. It suggests that, after the Moodies deposition, metasomatic pyrite formation commonly occurred north of the Inyoka Fault in the central BGB at 3.1–3.0 Ga.

Isotopic composition and geochemical features of ores of Dzhusa pyrite-polymetallic deposit (South Urals)

2019 ◽  
pp. 78-83
Author(s):  
E. I. Yartsev ◽  
I. V. Vikentyev ◽  
N. I. Eremin
Keyword(s):  
Isotopic Composition ◽  
Inductively Coupled Plasma ◽  
Sulfur Isotopes ◽  
Ore Deposits ◽  
South Urals ◽  
Sulfur Isotopic Composition ◽  
Inductively Coupled ◽  
Icp Ms ◽  
Highly Sensitive ◽  
First Time

The sulfur isotopic composition was studied for the main morphological types and generation of sulfides composing the ore of the Dzhusinsky deposit, and the content of trace elements was analyzed using the highly sensitive method of mass spectrometry with inductively coupled plasma and laser sampling (LA-ICP-MS). Both types of studies were performed for ore deposits for the first time. According to the geochemistry of sulfur isotopes, its deep magmatic source was reconstructed, which made a predominant contribution to the ore-forming fluid. Using the modules of the STATISTICA, correlations were calculated and the patterns of distribution of micro impurities in sulfide minerals were revealed.

scholarly journals Sedimentary pyrite sulfur isotopes track the local dynamics of the Peruvian oxygen minimum zone

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Virgil Pasquier ◽  
David A. Fike ◽  
Itay Halevy
Keyword(s):  
Organic Carbon ◽  
Environmental Changes ◽  
Sulfur Isotopes ◽  
Oxygen Minimum Zone ◽  
Sulfur Cycle ◽  
Major Influence ◽  
Sedimentary Environments ◽  
Minimum Zone ◽  
Sulfate Reduction Rates ◽  
Oxygen Minimum

AbstractSulfur cycling is ubiquitous in sedimentary environments, where it mediates organic carbon remineralization, impacting both local and global redox budgets, and leaving an imprint in pyrite sulfur isotope ratios (δ34Spyr). It is unclear to what extent stratigraphic δ34Spyr variations reflect local aspects of the depositional environment or microbial activity versus global sulfur-cycle variations. Here, we couple carbon-nitrogen-sulfur concentrations and stable isotopes to identify clear influences on δ34Spyr of local environmental changes along the Peru margin. Stratigraphically coherent glacial-interglacial δ34Spyr fluctuations (>30‰) were mediated by Oxygen Minimum Zone intensification/expansion and local enhancement of organic matter deposition. The higher resulting microbial sulfate reduction rates led to more effective drawdown and 34S-enrichment of residual porewater sulfate and sulfide produced from it, some of which is preserved in pyrite. We identify organic carbon loading as a major influence on δ34Spyr, adding to the growing body of evidence highlighting the local controls on these records.

Phanerozoic Oxygen

2017 ◽  
Author(s):  
Donald Eugene Canfield
Keyword(s):  
Oxygen Consumption ◽  
Organic Carbon ◽  
Sea Level ◽  
Time Scale ◽  
Atmospheric Oxygen ◽  
Sea Level Change ◽  
Oxygen Production ◽  
Level Change ◽  
History Of ◽  
Geologic Processes

This chapter discusses the modeling of the history of atmospheric oxygen. The most recently deposited sediments will also be the most prone to weathering through processes like sea-level change or uplift of the land. Thus, through rapid recycling, high rates of oxygen production through the burial of organic-rich sediments will quickly lead to high rates of oxygen consumption through the exposure of these organic-rich sediments to weathering. From a modeling perspective, rapid recycling helps to dampen oxygen changes. This is important because the fluxes of oxygen through the atmosphere during organic carbon and pyrite burial, and by weathering, are huge compared to the relatively small amounts of oxygen in the atmosphere. Thus, all of the oxygen in the present atmosphere is cycled through geologic processes of oxygen liberation (organic carbon and pyrite burial) and consumption (weathering) on a time scale of about 2 to 3 million years.

Changes of Ionic and Oxygen Isotopic Composition of the Snowpack at the Glacier Austre Okstindbreen, Norway, 1995

1998 ◽  
Vol 29 (1) ◽  
pp. 1-20 ◽  
Author(s):  
Peter Raben ◽  
Wilfred H. Theakstone
Keyword(s):  
Isotopic Composition ◽  
Sea Level ◽  
Oxygen Isotopes ◽  
Oxygen Isotopic Composition ◽  
Isotopic Ratios ◽  
Vertical Variations ◽  
Oxygen Isotopic ◽  
The Difference ◽  
Liquid Precipitation ◽  
Different Altitudes

Marked vertical variations of ions and oxygen isotopes were present in the snowpack at the glacier Austre Okstindbreen during the pre-melting phase in 1995 at sites between 825 m and 1,470 m above sea level. As the first meltwater percolated from the top of the pack, ions were moved to a greater depth, but the isotopic composition remained relatively unchanged. Ions continued to move downwards through the pack during the melting phase, even when there was little surface melting and no addition of liquid precipitation. The at-a-depth correlation between ionic concentrations and isotopic ratios, strong in the pre-melting phase, weakened during melting. In August, concentrations of Na+ and Mg2+ ions in the residual pack were low and vertical variations were slight; 18O enrichment had occurred. The difference of the time at which melting of the snowpack starts at different altitudes influences the input of ions and isotopes to the underlying glacier.

scholarly journals Holocene sea level and climate interactions on wet dune slack evolution in SW Portugal: A model for future scenarios?

The Holocene ◽  
2018 ◽  
Vol 29 (1) ◽  
pp. 26-44 ◽  
Author(s):  
Manel Leira ◽  
Maria C Freitas ◽  
Tania Ferreira ◽  
Anabela Cruces ◽  
Simon Connor ◽  
...  
Keyword(s):  
Sea Level Rise ◽  
Sea Level ◽  
Environmental Changes ◽  
Sediment Accumulation ◽  
High Energy ◽  
Sediment Supply ◽  
Dune Slack ◽  
Ecological Stability ◽  
The Holocene ◽  
Climate Interactions

We examine the Holocene environmental changes in a wet dune slack of the Portuguese coast, Poço do Barbarroxa de Baixo. Lithology, organic matter, biological proxies and high-resolution chronology provide estimations of sediment accumulation rates and changes in environmental conditions in relation to sea-level change and climate variability during the Holocene. Results show that the wet dune slack was formed 7.5 cal. ka BP, contemporaneous with the last stages of the rapid sea-level rise. This depositional environment formed under frequent freshwater flooding and water ponding that allowed the development and post-mortem accumulation of abundant plant remains. The wetland evolved into mostly palustrine conditions over the next 2000 years, until a phase of stabilization in relative sea-level rise, when sedimentation rates slowed down to 0.04 mm yr−1, between 5.3 and 2.5 cal. ka BP. Later, about 0.8 cal. ka BP, high-energy events, likely due to enhanced storminess and more frequent onshore winds, caused the collapse of the foredune above the wetlands’ seaward margin. The delicate balance between hydrology (controlled by sea-level rise and climate change), sediment supply and storminess modulates the habitat’s resilience and ecological stability. This underpins the relevance of integrating past records in coastal wet dune slacks management in a scenario of constant adaptation processes.

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