We report novel analytical procedures allowing for the concurrent determination of the stable and mass-independent Cr isotopic composition of silicate materials by multiple collector inductively coupled mass spectrometry (MC-ICPMS). In particular, we focus on improved precision of the measurement of the neutron-rich isotope Cr. Because nitride and oxide interferences are a major obstacle to precise and accurateCr measurements by MC-ICPMS, our approach is designed to minimize these interferences. Based on repeat measurements of standards, we show that the mass-independent Cr andCr compositions can be routinely determined with an external reproducibility better than 2.5 and 5.8 ppm (2 sd), respectively. This represents at least a two-fold improvement compared to previous studies. Although this approach uses significantly more Cr (30-60 μg) than analysis by thermal ionization mass spectrometry (TIMS), our result indicate that it is possible to obtain an external reproducibility of 19 ppm for the μCr when consuming amounts similar to that typically analyzed by TIMS (1 μg). In addition, the amount of time required for analysis by MC-ICPMS is much shorter thereby enabling a higher sample throughput. As a result of the improved analytical precision, we identified small apparent mass-independent differences between different synthetic Cr standards and bulk silicate Earth (BSE) when using the kinetic law for the mass bias correction. These differences are attributed to the Cr loss by equilibrium processes during production of the synthetic standards. The stable isotope data concurrently obtained have a precision of 0.05‰ Da , which is comparable to earlier studies. Comparison of the measured isotopic composition of four meteorites with published data indicates that Cr isotope data measured by the technique described here are accurate to stated uncertainties. The stable Cr composition of the Bilanga and NWA 2999 achondrites suggests that the differences in the stable Cr isotope composition of Earth and chondrites may reflect heterogeneity of their precursor material rather than Cr isotope fractionation during metal-silicate segregation of Earth. Lastly, a step wise dissolution experiment of the CI chondrite Ivuna reveals previously unknown carriers of large mass-dependent Cr stable isotope variations that co-vary with the known presence of carriers of large nucleosynthetic anomalies, demonstrating one advantage of this technique.
Refractory inclusions [calcium–aluminum-rich inclusions, (CAIs)] represent the oldest Solar System solids and provide information regarding the formation of the Sun and its protoplanetary disk. CAIs contain evidence of now extinct short-lived radioisotopes (e.g., 26 Al, 41 Ca, and 182 Hf) synthesized in one or multiple stars and added to the protosolar molecular cloud before or during its collapse. Understanding how and when short-lived radioisotopes were added to the Solar System is necessary to assess their validity as chronometers and constrain the birthplace of the Sun. Whereas most CAIs formed with the canonical abundance of 26 Al corresponding to 26 Al/ 27 Al of ∼5 × 10 −5 , rare CAIs with fractionation and unidentified nuclear isotope effects (FUN CAIs) record nucleosynthetic isotopic heterogeneity and 26 Al/ 27 Al of <5 × 10 −6 , possibly reflecting their formation before canonical CAIs. Thus, FUN CAIs may provide a unique window into the earliest Solar System, including the origin of short-lived radioisotopes. However, their chronology is unknown. Using the 182 Hf– 182 W chronometer, we show that a FUN CAI recording a condensation origin from a solar gas formed coevally with canonical CAIs, but with 26 Al/ 27 Al of ∼3 × 10 −6 . The decoupling between 182 Hf and 26 Al requires distinct stellar origins: steady-state galactic stellar nucleosynthesis for 182 Hf and late-stage contamination of the protosolar molecular cloud by a massive star(s) for 26 Al. Admixing of stellar-derived 26 Al to the protoplanetary disk occurred during the epoch of CAI formation and, therefore, the 26 Al– 26 Mg systematics of CAIs cannot be used to define their formation interval. In contrast, our results support 182 Hf homogeneity and chronological significance of the 182 Hf– 182 W clock.
Kilometre-scale geobodies of diagenetic origin have been documented for the first time in a high-resolution 3D seismic survey of the Upper Cretaceous chalks of the Danish Central Graben, North Sea Basin. Based on detailed geochemical, petrographic and petrophysical analyses, it is demonstrated that the geobodies are of an open-system diagenetic origin caused by ascending basin fluids guided by faults and stratigraphic heterogeneities. Increased amounts of porosity-occluding cementation, contact cement and/or high-density/high-velocity minerals caused an impedance contrast that can be mapped in seismic data, and represent a hitherto unrecognized, third type of heterogeneity in the chalk deposits in addition to the well-known sedimentological and structural features. The distribution of the diagenetic geobodies is controlled by porosity/permeability contrasts of stratigraphic origin, such as hardgrounds associated with formation tops, and the feeder fault systems. One of these, the Top Campanian Unconformity at the top of the Gorm Formation, is particularly effective and created a basin-wide barrier separating low-porosity chalk below from high-porosity chalk above (a Regional Porosity Marker, RPM). It is in particular in this upper high-porosity unit (Tor and EkofiskFormations) that the diagenetic geobodies occur, delineated by "Stratigraphy Cross-cutting Reflectors" (SCRs) of which eight different types have been distinguished. The geobodies have been interpreted as the result of: (i) escaping pore fluids due to top seal failure, followed by local mechanical compaction of highporous chalks, paired with (ii) ascension of basinal diagenetic fluids along fault systems that locally triggered cementation of calcite and dolomite within the chalk, causing increased contact cements and/or reducing porosity. The migration pathway of the fluids is marked by the SCRs, which are the outlines of highdensity bodies of chalk nested in highly porous chalks. This study, thus, provides new insights into the 3D relationship between fault systems, fluid migration and diagenesis in chalks and has important applications for basin modelling and reservoir characterization.---
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.