Geology topics

Torsten W. Vennemann

Publications and source records attributed to Torsten W. Vennemann.

5 recordsLinked to original sources

USGS2025

Foundational uncertainties in terminal Ediacaran chronostratigraphy revealed by high-precision zircon U-Pb geochronology of the Nama Group, Namibia

The Nama Group of southern Namibia and northwestern South Africa hosts the best-dated mixed carbonate-siliciclastic foreland basin succession of the terminal Ediacaran [ca. 551 million years (Ma) ago to <538 Ma] and is key for resolving the chronology of early metazoan evolution. Numerous silicified volcanic tuff interbeds are present, but differing interpretations regarding the fidelity of their ages lead to different regional stratigraphic correlations, especially for the Urusis Formation of the Schwarzrand Subgroup. An expanded record of the Urusis Formation is found in the Swartpunt area of southern Namibia, which has yielded an important metazoan biota. But the succession in this area is preserved as a series of thrusts at the leading edge of the Gariep orogenic belt and zircon U-Pb data show systematic age repetition. We use regional stratigraphic and structural mapping, integrated with carbonate carbon isotope (δ 13 C carb ) chemostratigraphy and high-precision radioisotope U-Pb zircon geochronology from outcrop and recently acquired drill core to develop a temporally calibrated basin-wide depositional model. This integrated dataset either reflects complex zircon reworking, inheritance, or potential analytical biases (Scenario 1) or the presence of a Gariep-related cryptic décollement within the Spitskop Member that has resulted in stratigraphic repetition (Scenario 2). We investigate the evidence for and against both scenarios and consider their implications for stratigraphic and δ 13 C carb correlations between the Swartpunt area and coeval exposures along the Orange River border with South Africa. Given that these issues are in an area that hosts numerous silicified ash beds and extensive exposure, an inability to confidently discount either scenario highlights a level of compounding uncertainty in zircon U-Pb geochronology that must be considered when attempting to build global chronostratigraphic frameworks. Scenario 1 implies that some of the weighted mean ages and Bayesian eruption ages from the Swartpunt area may be >1 Myr older than the depositional age of their respective ash beds when assuming existing stratigraphic correlations. If this scenario is preferred, then a cautious approach would be to consider all weighted mean zircon U-Pb ages from ash beds to reflect maximum depositional ages. Both scenarios support deposition of the Huns Member >540 Ma in the Swartpunt area if the oldest weighted mean age reported here represents a near-depositional age, which has significant implications for the temporal calibration of important terminal Ediacaran ichnofossil assemblages and future cyclostratigraphic studies. Stratigraphic correlations common to both scenarios allow us to temporally calibrate a basin evolution model for the Nama Group. Temporal trends in initial hafnium isotope (εHf) compositions of zircon grains from ash beds throughout the succession may support progressive crustal thickening associated with underplating of the Damara orogenic belt along the northern periphery of the Kalahari craton from ca. 547 Ma to ca. 538 Ma. The compilation of new and published zircon U-Pb ages may also imply that the locus of carbonate platform development migrated from north to south (present co-ordinates), tracking the migration of foredeep subsidence.

Earth-Science Reviews↗

USGS2021

Constraints on deep, CO2-rich degassing at arc volcanoes from solubility experiments on hydrous basaltic andesite of Pavlof Volcano, Alaska Peninsula, at 300 to 1200 MPa

The solubility of CO 2 in hydrous basaltic andesite was examined in f O2 -controlled experiments at a temperature of 1125 °C and pressures between 310–1200 MPa. Concentrations of dissolved H 2 O and CO 2 in experimental glasses were determined by ion microprobe calibrated on a subset of run glasses analyzed by high-temperature vacuum manometry. Assuming that the solubility of H 2 O in mafic melt is relatively well known, estimates of 𝑋H2Ofluid and 𝑃H2Ofluid in the saturating fluid were modeled, and by difference, values for 𝑋CO2fluid and 𝑃CO2fluid were obtained ( X CO2 ~0.5–0.9); f CO2 could be then calculated from the fluid composition, temperature, and pressure. Dissolved H 2 O over a range of 2.3–5.5 wt% had no unequivocal influence on the dissolution of CO 2 at the pressures and fluid compositions examined. For these H 2 O concentrations, dissolved CO 2 increases with f CO2 following an empirical power-law relation: dissolved CO 2 (ppmw) = 14.9−3.5+4.5 [ f CO2 (MPa)] 0.7±0.03 . The highest-pressure results plot farthest from this equation but are within its 1 standard-error uncertainty envelope. We compare our experimental data with three recent CO 2 -H 2 O solubility models: Papale et al. (2006) ; Iacono-Marziano et al. (2012) ; and Ghiorso and Gualda (2015) . The Papale et al. (2006) and Iacono-Marizano et al. (2012) models give similar results, both over-predicting the solubility of CO 2 in a melt of the Pavlof basaltic andesite composition across the f CO2 range, whereas the Ghiorso and Gualda (2015) model under-predicts CO 2 solubility. All three solubility models would indicate a strong enhancement of CO 2 solubility with increasing dissolved H 2 O not apparent in our results. We also examine our results in the context of previous high-pressure CO 2 solubility experiments on basaltic melts. Dissolved CO 2 correlates positively with mole fraction (Na+K+Ca)/Al across a compositional spectrum of trachybasalt-alkali basalt-tholeiite-icelandite-basaltic andesite. Shortcomings of current solubility models for a widespread arc magma type indicate that our understanding of degassing in the deep crust and uppermost mantle remains semi-quantitative. Experimental studies systematically varying concentrations of melt components (Mg, Ca, Na, K, Al, Si) may be necessary to identify solubility reactions, quantify their equilibrium constants, and thereby build an accurate and generally applicable solubility model.

Alaska↗

USGS2019

Geochemical and petrological diversity of mafic magmas from Mount St. Helens

Quaternary eruptive products in the Cascade arc include a variety of different basalt types. At Mount St. Helens (MSH), the most active volcano in the Cascades throughout the last 35 ka, three different mafic endmembers erupted at the end of the Castle Creek period (1900–1700 years B.P.): (1) high-field strength element (HFSE)-rich basalt enriched in K, Ti, P, and incompatible trace elements; (2) low-K olivine tholeiite (LKOT) with lower amounts of incompatible trace elements; and (3) calc-alkaline (arc-type) basaltic andesite with a typical subduction signature, i.e., enrichment in fluid-mobile large ion lithophile elements (LILE) relative to immobile high-field strength elements (HFSE). Each type has compositions projecting backwards to more primitive endmembers in the Cascades. Single units encompassing basaltic-to-basaltic andesitic compositions with intermediate trace-element abundances form two almost continuous trends towards basaltic andesite. These trends are interpreted to result from assimilation of pre-existing, more evolved, calc-alkaline material (and in one case mixing of different mafic magma types) during migration of the magmas through the crust. Most of the erupted basalts are porphyritic (10–30%) with an assemblage dominated by olivine and plagioclase and show disequilibrium textures preventing detailed reconstruction of mantle melting processes. Although typical hydrous arc basalt produced by flux melting in the mantle is absent in the eruptive products of MSH, arc-type basaltic andesite suggests its presence at depth. LKOT magmas are interpreted as decompression melts from the upper mantle, whereas HFSE-rich basalts are likely derived from the water-poor periphery of the main flux melting regime, potentially tapping a trace-element-enriched source. Primitive spinel compositions and whole-rock trace-element variations indicate at least two distinct, relatively fertile lherzolite sources for these two basalt types. Weak crustal zones associated with an old fracture system beneath MSH likely provide conduits for fast and isolated ascent of distinct batches of magma, bypassing the lower crustal mush zone. The eruption of the basalts through the upper crustal magma system and main edifice is consistent with an offset plumbing system suggested by geophysical data.

Washington↗

USGS2017

New biotite and muscovite isotopic reference materials, USGS57 and USGS58, for δ2H measurements–A replacement for NBS 30

The advent of continuous-flow isotope-ratio mass spectrometry (CF-IRMS) coupled with a high temperature conversion (HTC) system enabled faster, more cost effective, and more precise δ 2 H analysis of hydrogen-bearing solids. Accurate hydrogen isotopic analysis by on-line or off-line techniques requires appropriate isotopic reference materials (RMs). A strategy of two-point calibrations spanning δ 2 H range of the unknowns using two RMs is recommended. Unfortunately, the supply of the previously widely used isotopic RM, NBS 30 biotite, is exhausted. In addition, recent measurements have shown that the determination of δ 2 H values of NBS 30 biotite on the VSMOW-SLAP isotope-delta scale by on-line HTC systems with CF-IRMS may be unreliable because hydrogen in this biotite may not be converted quantitatively to molecular hydrogen. The δ 2 H VSMOW-SLAP values of NBS 30 biotite analyzed by on-line HTC systems can be as much as 21 mUr (or ‰) too positive compared to the accepted value of − 65.7 mUr, determined by only a few conventional off-line measurements. To ensure accurate and traceable on-line hydrogen isotope-ratio determinations in mineral samples, we here propose two isotopically homogeneous, hydrous mineral RMs with well-characterized isotope-ratio values, which are urgently needed. The U.S. Geological Survey (USGS) has prepared two such RMs, USGS57 biotite and USGS58 muscovite. The δ 2 H values were determined by both glassy carbon-based on-line conversion and chromium-based on-line conversion, and results were confirmed by off-line conversion. The quantitative conversion of hydrogen from the two RMs using the on-line HTC method was carefully evaluated in this study. The isotopic compositions of these new RMs with 1-σ uncertainties and mass fractions of hydrogen are: USGS57 (biotite) δ 2 H VSMOW-SLAP = − 91.5 ± 2.4 mUr ( n = 24) Mass fraction hydrogen = 0.416 ± 0.002% ( n = 4) Mass fraction water = 3.74 ± 0.02% ( n = 4) USGS58 (muscovite) δ 2 H VSMOW-SLAP = − 28.4 ± 1.6 mUr ( n = 24) Mass fraction hydrogen = 0.448 ± 0.002% ( n = 4) Mass fraction water = 4.03 ± 0.02% ( n = 4). These δ 2 H VSMOW-SLAP values encompass typical ranges for solid unknowns of crustal and mantle origin and are available to users for recommended two-point calibration.

Chemical Geology↗

USGS2014

Caution on the use of NBS 30 biotite for hydrogen-isotope measurements with on-line high-temperature conversion systems

RATIONALE The supply of NBS 30 biotite is nearly exhausted. During measurements of NBS 30 and potential replacements, reproducible δ 2 H VSMOW-SLAP values could not be obtained by three laboratories using high-temperature conversion (HTC) systems. The cause of this issue has been investigated using the silver-tube technique for hydrogen-isotope measurements of water. METHODS The δ 2 H VSMOW-SLAP values of NBS 30 biotite, other biotites, muscovites, and kaolinite with different particle sizes, along with IAEA-CH-7 polyethylene, and reference waters and NBS 22 oil that were sealed in silver-tube segments, were measured. The effect of absorbed water on mineral surfaces was investigated with waters both enriched and depleted in 2 H. The quantitative conversion of hydrogen from biotite into gaseous hydrogen as a function of mass and particle size was also investigated. RESULTS The δ 2 H VSMOW-SLAP values of NBS 30 obtained by three laboratories were as much as 21 ‰ too high compared with the accepted value of −65.7 ‰, determined by conventional off-line measurements. The experiments showed a strong correlation between grain size and the δ 2 H VSMOW-SLAP value of NBS 30 biotite, but not of biotites with lower iron content. The δ 2 H VSMOW-SLAP values of NBS 30 as a function of particle size show a clear trend toward −65.7 ‰ with finer grain size. CONCLUSIONS Determination of the δ 2 H VSMOW-SLAP values of hydrous minerals and of NBS 30 biotite by on-line HTC systems coupled to isotope-ratio mass spectrometers may be unreliable because hydrogen in this biotite may not be converted quantitatively into molecular hydrogen. Extreme caution in the use and interpretation of δ 2 H VSMOW-SLAP on-line measurements of hydrous minerals is recommended.

Rapid Communications in Mass Spectrometry↗