The composition of the Earth

Knowledge of temperature and pressure, however qualitative, has been central to our views of geology since at least the early 19th century. In 1822, for example, Charles Daubeny presented what may be the very first “Geological Thermometer,” comparing temperatures of various geologic processes (Torrens 2006). Daubeny (1835) may even have been the first to measure the temperature of a lava flow, by laying a thermometer on the top of a flow at Vesuvius—albeit several months following the eruption, after intervening rain (his estimate was 390°F). In any case, pressure ( P ) and temperature ( T ) estimation lie at the heart of fundamental questions: How hot is Earth, and at what rate has the planet cooled. Are volcanoes the products of thermally driven mantle plumes? Where are magmas stored, and how are they transported to the surface—and how do storage and transport relate to plate tectonics? Well-calibrated thermometers and barometers are essential tools if we are to fully appreciate the driving forces and inner workings of volcanic systems.

This chapter presents methods to estimate the P-T conditions of volcanic and other igneous processes. The coverage includes a review of existing geothermometers and geobarometers, and a presentation of approximately 30 new models, including a new plagioclase-liquid hygrometer. Our emphasis is on experimentally calibrated “thermobarometers,” based on analytic expressions using P or T as dependent variables. For numerical reasons (touched on below) such expressions will always provide the most accurate means of P-T estimation, and are also most easily employed. Analytical expressions also allow error to be ascertained; in the absence of estimates of error, P-T estimates are nearly meaningless. This chapter is intended to complement the chapters by Anderson et al. (2008), who cover granitic systems, and by Blundy and Cashman (2008) and Hansteen and Klugel (2008), who consider additional methods …

Thermometers and Barometers for Volcanic Systems

We present new reference values for the NIST SRM 610–617 glasses following ISO guidelines and the International Association of Geoanalysts’ protocol. Uncertainties at the 95% confidence level (CL) have been determined for bulk- and micro-analytical purposes. In contrast to former compilation procedures, this approach delivers data that consider present-day requirements of data quality. New analytical data and the nearly complete data set of the GeoReM database were used for this study. Data quality was checked by the application of the Horwitz function and by a careful investigation of analytical procedures. We have determined quantitatively possible element inhomogeneities using different test portion masses of 1, 0.1 and 0.02 μg. Although avoiding the rim region of the glass wafers, we found moderate inhomogeneities of several chalcophile/siderophile elements and gross inhomogeneities of Ni, Se, Pd and Pt at small test portion masses. The extent of inhomogeneity was included in the determination of uncertainties. While the new reference values agree with the NIST certified values with the one exception of Mn in SRM 610, they typically differ by as much as 10% from the Pearce et al. (1997) values in current use. In a few cases (P, S, Cl, Ta, Re) the discrepancies are even higher.



Nous presentons des nouvelles valeurs de reference pour les verres NIST SRM 610–617 en suivant les recommandations de l’ISO et le protocole de l’IAG. Les incertitudes au niveau de confiance de 95% ont ete determinees a des fins d’analyse totale et de micro-analyse. Contrairement aux procedures de compilation precedentes, cette approche fournit des donnees qui tiennent compte des exigences actuelles dans la qualite des donnees. De nouvelles donnees analytiques et le jeu de donnees presque complet de la base de donnees GeoReM ont ete utilises pour cette etude. La qualite des donnees a ete verifiee par l’application de la fonction de Horwitz et par un examen minutieux des procedures analytiques. Nous avons determine quantitativement les possibles inhomogeneites d’element en utilisant des prises d’essai de masses differentes correspondant a 1, 0.1 et 0.02 μg. Bien que nous ayons evite les zones de bordure des disques de verre, nous avons trouve des inhomogeneites moderees pour plusieurs elements chalcophiles/siderophiles et des inhomogeneites flagrantes de Ni, Se, Pd et Pt pour les prises d’essai de petites masses. La mesure d’inhomogeneite a ete incluse dans la determination des incertitudes. Alors que les nouvelles valeurs de reference sont en accord avec les valeurs NIST certifiees a la seule exception du Mn dans SRM 610, elles sont generalement differentes, avec des ecarts de pres de 10%, des valeurs de Pearce et al. (1997) qui sont d’un usage courant. Dans quelques cas (P, S, Cl, Ta, Re), les ecarts sont encore plus eleves.

Determination of Reference Values for NIST SRM 610–617 Glasses Following ISO Guidelines

Data Reduction And Error Analysis For The Physical Sciences

Calibration of the geological time scale is achieved by independent radioisotopic and astronomical dating, but these techniques yield discrepancies of ∼1.0% or more, limiting our ability to reconstruct Earth history. To overcome this fundamental setback, we compared astronomical and 40 Ar/ 39 Ar ages of tephras in marine deposits in Morocco to calibrate the age of Fish Canyon sanidine, the most widely used standard in 40 Ar/ 39 Ar geochronology. This calibration results in a more precise older age of 28.201 ± 0.046 million years ago (Ma) and reduces the 40 Ar/ 39 Ar method9s absolute uncertainty from ∼2.5 to 0.25%. In addition, this calibration provides tight constraints for the astronomical tuning of pre-Neogene successions, resulting in a mutually consistent age of ∼65.95 Ma for the Cretaceous/Tertiary boundary.

https://science.sciencemag.org/content/sci/320/5875/500.full.pdf

Synchronizing Rock Clocks of Earth History

The formation and alteration of the Renazzo-like carbonaceous chondrites II: Linking O-isotope composition and oxidation state of chondrule olivine

Highly 15N-enriched chondritic clasts in the CB/CH-like meteorite Isheyevo

The determination of an isotope ratio by secondary ion mass spectrometry (SIMS) traditionally involves averaging a number of ratios collected over the course of a measurement We show that this method leads to an additive positive bias in the expectation value of the estimated ratio that is approximately equal to the true ratio divided by the counts of the denominator isotope of an individual ratio This bias does not decrease as the number of ratios used in the average increases By summing all counts in the numerator isotope, then dividing by the sum of counts in the denominator isotope, the estimated ratio is less biased: the bias is approximately equal to the ratio divided by the summed counts of the denominator isotope over the entire measurement We propose a third ratio estimator (Beale’s estimator) that can be used when the bias from the summed counts is unacceptably large for the hypothesis being tested We derive expressions for the variance of these ratio estimators as well as the conditions under which they are normally distributed Finally, we investigate a SIMS dataset showing the effects of ratio bias, and discuss proper ratio estimation for SIMS analysis

Ratio Estimation in SIMS Analysis

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We review recent results on O- and Mg-isotope compositions of refractory grains (corundum, hibonite) and calcium, aluminum-rich inclusions (CAIs) from unequilibrated ordinary and carbonaceous chondrites. We show that these refractory objects originated in the presence of nebular gas enriched in 16O to varying degrees relative to the standard mean ocean water value: the Δ17OSMOW value ranges from approximately −16‰ to −35‰, and recorded heterogeneous distribution of 26Al in their formation region: the inferred (26Al/27Al)0 ranges from approximately 6.5 × 10−5 to <2 × 10−6. There is no correlation between O- and Mg-isotope compositions of the refractory objects: 26Al-rich and 26Al-poor refractory objects have similar O-isotope compositions. We suggest that 26Al was injected into the 26Al-poor collapsing protosolar molecular cloud core, possibly by a wind from a neighboring massive star, and was later homogenized in the protoplanetary disk by radial mixing, possibly at the canonical value of 26Al/27Al ratio (approximately 5 × 10−5). The 26Al-rich and 26Al-poor refractory grains and inclusions represent different generations of refractory objects, which formed prior to and during the injection and homogenization of 26Al. Thus, the duration of formation of refractory grains and CAIs cannot be inferred from their 26Al-26Mg systematics, and the canonical (26Al/27Al)0 does not represent the initial abundance of 26Al in the solar system; instead, it may or may not represent the average abundance of 26Al in the fully formed disk. The latter depends on the formation time of CAIs with the canonical 26Al/27Al ratio relative to the timing of complete delivery of stellar 26Al to the solar system, and the degree of its subsequent homogenization in the disk. The injection of material containing 26Al resulted in no observable changes in O-isotope composition of the solar system. Instead, the variations in O-isotope compositions between individual CAIs indicate that O-isotope composition of the CAI-forming region varied, because of coexisting of 16O-rich and 16O-poor nebular reservoirs (gaseous and/or solid) at the birth of the solar system, or because of rapid changes in the O-isotope compositions of these reservoirs with time, e.g., due to CO self-shielding in the disk.

https://onlinelibrary.wiley.com/doi/pdf/10.1111/maps.12008

Gary R. Huss

Papers

The formation and alteration of the Renazzo-like carbonaceous chondrites II: Linking O-isotope composition and oxidation state of chondrule olivine

Highly 15N-enriched chondritic clasts in the CB/CH-like meteorite Isheyevo

Ratio Estimation in SIMS Analysis

Heterogeneous distribution of 26Al at the birth of the solar system: Evidence from refractory grains and inclusions

Magmatic water in the martian meteorite Nakhla