Thomas Zack

Bio: Thomas Zack is an academic researcher from University of Gothenburg. The author has contributed to research in topics: Zircon & Metamorphism. The author has an hindex of 42, co-authored 133 publications receiving 6464 citations. Previous affiliations of Thomas Zack include University of Göttingen & University of Adelaide.

MPI-DING reference glasses for in situ microanalysis: New reference values for element concentrations and isotope ratios

Abstract: We present new analytical data of major and trace elements for the geological MPI-DING glasses KL2-G, ML3B-G, StHs6/80-G, GOR128-G, GOR132-G, BM90/21-G, T1-G, and ATHO-G. Different analytical methods were used to obtain a large spectrum of major and trace element data, in particular, EPMA, SIMS, LA-ICPMS, and isotope dilution by TIMS and ICPMS. Altogether, more than 60 qualified geochemical laboratories worldwide contributed to the analyses, allowing us to present new reference and information values and their uncertainties (at 95% confidence level) for up to 74 elements. We complied with the recommendations for the certification of geological reference materials by the International Association of Geoanalysts (IAG). The reference values were derived from the results of 16 independent techniques, including definitive (isotope dilution) and comparative bulk (e.g., INAA, ICPMS, SSMS) and microanalytical (e.g., LA-ICPMS, SIMS, EPMA) methods. Agreement between two or more independent methods and the use of definitive methods provided traceability to the fullest extent possible. We also present new and recently published data for the isotopic compositions of H, B, Li, O, Ca, Sr, Nd, Hf, and Pb. The results were mainly obtained by high-precision bulk techniques, such as TIMS and MC-ICPMS. In addition, LA-ICPMS and SIMS isotope data of B, Li, and Pb are presented.

Temperature dependence of Zr in rutile: empirical calibration of a rutile thermometer

Abstract: Rutile is an important carrier of high field strength elements (HFSE; Zr, Nb, Mo, Sn, Sb, Hf, Ta, W). Its Zr content is buffered in systems with quartz and zircon as coexisting phases. The effects of temperature (T) and pressure (P) on the Zr content in rutile have been empirically calibrated in this study by analysing rutile–quartz–zircon assemblages of 31 metamorphic rocks spanning a T range from 430 to 1,100°C. Electron microprobe measurements show that Zr concentrations in rutile vary from 30 to 8,400 ppm across this temperature interval, correlating closely with metamorphic grade. The following thermometer has been formulated based on the maximum Zr contents of rutile included in garnet and pyroxene: % MathType!Translator!2!1!AMS LaTeX.tdl!TeX -- AMS-LaTeX! % MathType!MTEF!2!1!+- % feaafeart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn % hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr % 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9 % vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x % fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaamivaiaabI % cacaqGPbGaaeOBaiaaysW7daahaaWcbeqaaiablIHiVbaakiaaboea % caqGPaGaaeiiaiaab2dacaqGGaGaaeymaiaabkdacaqG3aGaaeOlai % aabIdacaaMc8Uaey41aqRaaeiBaiaab6gacaqGGaGaaeikaiaabQfa % caqGYbGaaGPaVlaabMgacaqGUbGaaGPaVlaabchacaqGWbGaaeyBai % aabMcacaaMc8UaeyOeI0Iaaeymaiaabcdaaaa!5848! $$ T{\text{(in}}\;^ \circ {\text{C) = 127}}{\text{.8}}\, \times {\text{ln (Zr}}\,{\text{in}}\,{\text{ppm)}}\, - {\text{10}} $$ No pressure dependence was observed. An uncertainty in absolute T of ±50°C is inherited from T estimates of the natural samples used. A close approach to equilibrium of Zr distribution between zircon and rutile is suggested based on the high degree of reproducability of Zr contents in rutiles from different rock types from the same locality. At a given locality, the calculated range in T is mostly ±10°C, indicating the geological and analytical precision of the rutile thermometer. Possible applications of this new geothermometer are discussed covering the fields of ultrahigh temperature (UHT) granulites, sedimentary provenance studies and metamorphic field gradients.

New thermodynamic models and revised calibrations for the Ti-in-zircon and Zr-in-rutile thermometers

Abstract: The models recognize that ZrSiO4, ZrTiO4, and TiSiO4, but not ZrO2 or TiO2, are independently variable phase components in zircon. Accordingly, the equilibrium controlling the Zr content of rutile coexisting with zircon is ZrSiO4 = ZrO2 (in rutile) + SiO2. The equilibrium controlling the Ti content of zircon is either ZrSiO4 + TiO2 = ZrTiO4 + SiO2 or TiO2 + SiO2 = TiSiO4, depending whether Ti substitutes for Si or Zr. The Zr content of rutile thus depends on the activity of SiO2 $$(a_{\text{SiO}_{2}})$$ as well as T, and the Ti content of zircon depends on $$a_{\text{SiO}_{2}}$$ and $$a_{\text{TiO}_{2}}$$ as well as T. New and published experimental data confirm the predicted increase in the Zr content of rutile with decreasing $$a_{\text{SiO}_{2}},$$ and unequivocally demonstrate that the Ti content of zircon increases with decreasing $$a_{\text{SiO}_{2}}$$ . The substitution of Ti in zircon therefore is primarily for Si. Assuming a constant effect of P, unit $$a_{\text{ZrSiO}_{4}},$$ and that $$a_{\text{ZrO}_{2}}$$ and $$a_{\text{ZrTiO}_{4}}$$ are proportional to ppm Zr in rutile and ppm Ti in zircon, [log(ppm Zr-in-rutile) + log $$a_{\text{SiO}_{2}}$$ ] = A1 + B1/T(K) and [log(ppm Ti-in-zircon) + log $$a_{\text{SiO}_{2}}$$ − log $$a_{\text{TiO}_{2}}$$ ] = A2 + B2/T, where the A and B are constants. The constants were derived from published and new data from experiments with $$a_{\text{SiO}_{2}}$$ buffered by either quartz or zircon + zirconia, from experiments with $$a_{\text{SiO}_{2}}$$ defined by the Zr content of rutile, and from well-characterized natural samples. Results are A1 = 7.420 ± 0.105; B1 = −4,530 ± 111; A2 = 5.711 ± 0.072; B2 = −4,800 ± 86 with activity referenced to α-quartz and rutile at P and T of interest. The zircon thermometer may now be applied to rocks without quartz and/or rutile, and the rutile thermometer applied to rocks without quartz, provided that $$a_{\text{SiO}_{2}}$$ and $$a_{\text{TiO}_{2}}$$ are estimated. Maximum uncertainties introduced to zircon and rutile thermometry by unconstrained $$a_{\text{SiO}_{2}}$$ and $$a_{\text{TiO}_{2}}$$ can be quantitatively assessed and are ≈60 to 70°C at 750°C. A preliminary assessment of the dependence of the two thermometers on P predicts that an uncertainty of ±1 GPa introduces an additional uncertainty at 750°C of ≈50°C for the Ti-in-zircon thermometer and of ≈70 to 80°C for the Zr-in-rutile thermometer.

Crystallization thermometers for zircon and rutile

Abstract: Zircon and rutile are common accessory minerals whose essential structural constituents, Zr, Ti, and Si can replace one another to a limited extent. Here we present the combined results of high pressure–temperature experiments and analyses of natural zircons and rutile crystals that reveal systematic changes with temperature in the uptake of Ti in zircon and Zr in rutile. Detailed calibrations of the temperature dependencies are presented as two geothermometers—Ti content of zircon and Zr content of rutile—that may find wide application in crustal petrology. Synthetic zircons were crystallized in the presence of rutile at 1–2 GPa and 1,025–1,450°C from both silicate melts and hydrothermal solutions, and the resulting crystals were analyzed for Ti by electron microprobe (EMP). To augment and extend the experimental results, zircons hosted by five natural rocks of well-constrained but diverse origin (0.7–3 GPa; 580–1,070°C) were analyzed for Ti, in most cases by ion microprobe (IMP). The combined experimental and natural results define a log-linear dependence of equilibrium Ti content (expressed in ppm by weight) upon reciprocal temperature: $$\log ({\text{Ti}}_{{{\text{zircon}}}}) = (6.01 \pm 0.03) - \frac{{5080 \pm 30}}{{T\;(\hbox{K})}}.$$ In a strategy similar to that used for zircon, rutile crystals were grown in the presence of zircon and quartz (or hydrous silicic melt) at 1–1.4 GPa and 675–1,450°C and analyzed for Zr by EMP. The experimental results were complemented by EMP analyses of rutile grains from six natural rocks of diverse origin spanning 0.35–3 GPa and 470–1,070°C. The concentration of Zr (ppm by weight) in the synthetic and natural rutiles also varies in log-linear fashion with T −1: $$\log ({\text{Zr}}_{{{\text{rutile}}}}) = (7.36 \pm 0.10) - \frac{{4470 \pm 120}}{{T\;(\hbox{K})}}.$$ The zircon and rutile calibrations are consistent with one another across both the synthetic and natural samples, and are relatively insensitive to changes in pressure, particularly in the case of Ti in zircon. Applied to natural zircons and rutiles of unknown provenance and/or growth conditions, the thermometers have the potential to return temperatures with an estimated uncertainty of ±10 ° or better in the case of zircon and ±20° or better in the case of rutile over most of the temperature range of interest (∼400–1,000°C). Estimates of relative temperature or changes in temperature (e.g., from zoning profiles in a single mineral grain) made with these thermometers are subject to analytical uncertainty only, which can be better than ±5° depending on Ti or Zr concentration (i.e., temperature), and also upon the analytical instrument (e.g., IMP or EMP) and operating conditions.

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

Abstract: 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.

GeoReM: A New Geochemical Database for Reference Materials and Isotopic Standards

Abstract: We have developed a new database named GeoReM (http://georem.mpch-mainz.gwdg.de) for reference materials and isotopic standards of geochemical and mineralogical interest. Reference samples include rock powders originating from the USGS, GSJ, GIT-IWG, synthetic and natural reference glasses originating from NIST, USGS, MPI-DING, as well as mineral (e.g., 91500 zircon), isotopic (e.g., La Jolla, E&A, NIST SRM 981), river water and seawater reference materials. GeoReM is a relational database, which strongly follows the concept of the three EARTHCHEM databases. It contains published analytical and compilation values (major and trace element concentrations, radiogenic and stable isotope ratios), important metadata about the analytical values, such as uncertainty, uncertainty type, method and laboratory. Sample information and references are also included. Three different ways of interrogating the database are possible: (1) sample names or material types, (2) chemical criteria and (3) bibliography. Some typical applications are described. GeoReM currently (October 2005) contains more than 750 geological reference materials, 6000 individual sets of results and references to 650 publications.