How Two Unassuming Elements, Re and Os, Assumed Acclaim in the Geosciences

Author(s):  
Holly Stein

<p>Re and Os (rhenium and osmium) are chalcophile-siderophile elements (transition metals) with a unique position in isotope geochemistry. Unlike other commonly used decay schemes for radiometric dating, these metals take residency in resource-related media, for example, sulfide minerals, the organic component in black shales, coals, and bitumens and oils. In short, the reducing environment is their haven whereas under oxidizing conditions, Re and Os become unmoored and the radiometric clock becomes compromised. The clock is not temperature sensitive, and its applicability spans Early Archean to Pleistocene.</p><p>This Bunsen Medal lecture will explore and review the challenges in bringing Re-Os from the meteorite-mantle community into the crustal environment. At the center of it all is our ability to turn geologic observation into a thoughtful sampling strategy. The possibility to date ore deposits was an obvious application, and molybdenite [Mo(Re)S<sub>2</sub>], rarely with significant common Os and lacking overgrowths, became an overnight superstar, yielding highly precise, accurate, and reproducible ages. Yet, molybdenite presented our first sampling challenge with recognition of a puzzling parent-daughter (<sup>187</sup>Re-<sup>187</sup>Os) decoupling in certain occurrences. A strategic sampling procedure was employed. From there, the diversity of applications spread, as molybdenite is also an accessory mineral in many granitoids, and can be a common trace sulfide in metamorphic rocks conformable with and/or cross-cutting foliation linking timing and deformation. Pyrite and arsenopyrite can also be readily dated.</p><p>Applications jumped from sulfides to organic matter. Extracting and dating the organic (hydrogeneous) component in black shales gives us Re-Os ages for sedimentary units in the Geologic Time Scale. This led to construction of an Os isotope seawater curve – an ongoing process. Unlike the well-known Sr seawater curve, the short residence time of Os in the oceans creates a high-definition time record with unambiguous high-amplitude swings in <sup>187</sup>Os/<sup>188</sup>Os. Re-Os puts time pins into the biostratigraphic record, and we have even directly dated fossils. Re-Os opened the door for a new generation of paleoclimate studies to evaluate seawater conditions at the time of organic blooms and organic sequestration in bottom mud. Uplift and continental erosion can be balanced with hydrothermal input into oceans based on changes in the Os isotope composition of seawater. The timing and connectivity of opening seaways can be determined, and the timing of glaciation and deglaciation events can be globally correlated. The timing and instigators of mass extinctions are carried in the Re-Os record. A meteorite impact places an enormous scar in the Os isotope record as seawater drops toward mantle values and recovers in a few thousand years. Most recently, Re-Os has transformed our understanding of the events and fluids involved in the construction of whole petroleum systems.</p><p>Looking to the future, what kinds of data sets will be explored and what are the interdisciplinary skill sets needed to interpret those data? Re-Os will continue to provide us with new ways to dismantle geologic media for new scientific understanding of processes that have shaped our lithosphere, biosphere and hydrosphere and their intersection and exchange.</p>

2021 ◽  
Author(s):  
Holly Stein

<p>Re and Os (rhenium and osmium) are chalcophile-siderophile elements (transition metals) with a unique position in isotope geochemistry.  Unlike other commonly used decay schemes for radiometric dating, these metals take residency in resource-related media, for example, sulfide minerals, the organic component in black shales, coals, and bitumens and oils.  In sum, the reducing environment is their haven whereas under oxidizing conditions, Re and Os become unmoored and the radiometric clock becomes compromised.  The clock is not temperature sensitive, and its applicability spans Early Archean to Pleistocene. </p><p>This Bunsen Medal lecture will explore and review the challenges in bringing Re-Os from the meteorite-mantle community into the crustal environment.  At the center of it all is our ability to turn geologic observation into a thoughtful sampling strategy.  The potential to date ore deposits was an obvious application and molybdenite [Mo(Re)S<sub>2</sub>], rarely with significant common Os and rarely with overgrowths, became an overnight superstar, yielding highly precise, accurate, and reproducible ages.  Yet, molybdenite presented our first sampling challenge with recognition of a puzzling parent-daughter (<sup>187</sup>Re-<sup>187</sup>Os) decoupling in certain occurrences.  A strategic sampling procedure was employed.  From there, the diversity of applications spread, as molybdenite is also an accessory mineral in many granitoids, and can be a common trace sulfide in metamorphic rocks.  Whether conformable with and/or crosscutting foliation, molybdenite ages define the timing of deformational events.  Pyrite and arsenopyrite can also be readily dated. </p><p>Applications jumped from sulfides to organic matter.  The hydrogenous component from organic matter in black shales gives us Re-Os ages in the sedimentary record for the Geologic Time Scale.  This led to construction of an Os isotope seawater curve – an ongoing process.  Unlike the well-known Sr seawater curve, the short residence time of Os in the oceans creates a high-definition time record with unambiguous high-amplitude swings in <sup>187</sup>Os/<sup>188</sup>Os.  Re-Os puts time pins into the biostratigraphic record, and we have even directly dated fossils.  Re-Os opened the door for a new generation of paleoclimate studies to evaluate seawater conditions at the time of organic blooms and organic sequestration in bottom mud.  Uplift and continental erosion can be balanced with hydrothermal input into oceans based on changes in the Os isotope composition of seawater.  The timing and connectivity of opening seaways can be determined, and the timing of glaciation and deglaciation events can be globally correlated.  The timing and instigators of mass extinctions are carried in the Re-Os record.  A major meteorite impact places an enormous scar in the Os isotope record as seawater drops toward mantle values but recovers in just a few thousand years.  Most recently, Re-Os has transformed our understanding of the events and fluids involved in construction of whole petroleum systems. </p><p>Looking to the future, what kinds of data sets will be explored and what are the interdisciplinary skill sets needed to interpret those data?  Re-Os will continue to provide us with new ways to dismantle geologic media for new scientific understanding of processes that have shaped our lithosphere, biosphere and hydrosphere, recording their intersection and exchange. </p>


Minerals ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 449
Author(s):  
Kirill S. Ivanov ◽  
Valery V. Maslennikov ◽  
Dmitry A. Artemyev ◽  
Aleksandr S. Tseluiko

In the Bazhenov Formation, framboidal clusters and nodular pyrite formed in the dysoxic–anoxic interface within organic-rich sediments. Some nodule-like pyritized bituminous layers and pyrite nodules are similar to pyritized microbial mat fragments by the typical fine laminated structure. Framboidal pyrite of the Bazhenov Formation is enriched in redox-sensitive elements such as Mo, V, Au, Cu, Pb, Ag, Ni, Se, and Zn in comparison with the host shales and nodular pyrite. Nodular pyrite has higher concentrations of As and Sb, only. Strong positive correlations that can be interpreted as nano-inclusions of organic matter (Mo, V, Au), sphalerite (Zn, Cd, Hg, Sn, In, Ga, Ge), galena (Pb, Bi, Sb, Te, Ag, Tl), chalcopyrite (Cu, Se) and tennantite (Cu, As, Sb, Bi, Te, Ag, Tl) and/or the substitution of Co, Ni, As and Sb into the pyrite. On the global scale, pyrite of the Bazhenov Formation is very similar to pyrite from highly metalliferous bituminous black shales, associated, as a rule, with gas and oil-and-gas deposits. Enrichment with Mo and lower Co and heavy metals indicate a higher influence of seawater during formation of pyrite from the Bazhenov Formation in comparison to different styles of ore deposits. Transitional elements such as Zn and Cu in pyrite of the Bazhenov Formation has resulted from either a unique combination of the erosion of Cu–Zn massive sulfide deposits of the Ural Mountains from one side and the simultaneous manifestation of organic-rich gas seep activity in the West Siberian Sea from another direction.


2008 ◽  
Vol 248 (3-4) ◽  
pp. 195-212 ◽  
Author(s):  
V.G. Batanova ◽  
G.E. Brügmann ◽  
B.A. Bazylev ◽  
A.V. Sobolev ◽  
V.S. Kamenetsky ◽  
...  

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Tatsuo Nozaki ◽  
Junichiro Ohta ◽  
Takaaki Noguchi ◽  
Honami Sato ◽  
Akira Ishikawa ◽  
...  

AbstractMeteorite impacts have caused catastrophic perturbations to the global environment and mass extinctions throughout the Earth’s history. Here, we present petrographic and geochemical evidence of a possible impact ejecta layer, dating from about 11 Ma, in deep-sea clayey sediment in the Northwest Pacific. This clay layer has high platinum group element (PGE) concentrations and features a conspicuous negative Os isotope anomaly (187Os/188Os as low as ~0.2), indicating an influx of extraterrestrial material. It also contains abundant spherules that include pseudomorphs suggestive of porphyritic olivine as well as spinel grains with euhedral, dendritic and spherical forms and NiO contents as great as 23.3 wt%, consistent with impact ejecta. Osmium isotope stratigraphy suggests a most plausible depositional age of ~11 Ma (Miocene) for this layer, as determined by fitting with the seawater evolution curve. No large impact crater of this age is known on land, even within the relatively large uncertainty range of the relative Os age. Thus, we suggest that an unrecognised impact event in the middle or late Miocene produced the impact ejecta layer of the Northwest Pacific.


2014 ◽  
Vol 29 (6) ◽  
pp. 1017-1023 ◽  
Author(s):  
Yue-Heng Yang ◽  
Fu-Yuan Wu ◽  
Yang Li ◽  
Jin-Hui Yang ◽  
Lie-Wen Xie ◽  
...  

Bastnaesite, a common accessory mineral in REE ore deposits, is ideal for U–Pb isotopic dating because of its relatively high U and Th contents.


2014 ◽  
Vol 400 ◽  
pp. 33-44 ◽  
Author(s):  
Claudio Marchesi ◽  
Christopher W. Dale ◽  
Carlos J. Garrido ◽  
D. Graham Pearson ◽  
Delphine Bosch ◽  
...  

1998 ◽  
Vol 62 (13) ◽  
pp. 2293-2310 ◽  
Author(s):  
O.M. Burnham ◽  
N.W. Rogers ◽  
D.G. Pearson ◽  
P.W. van Calsteren ◽  
C.J. Hawkesworth

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