Geology topics

Nobumichi Shimizu

Publications and source records attributed to Nobumichi Shimizu.

3 recordsLinked to original sources

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↗

USGS2014

Sulfur isotope fractionation between fluid and andesitic melt: An experimental study

Glasses produced from decompression experiments conducted by Fiege et al. (2014a) were used to investigate the fractionation of sulfur isotopes between fluid and andesitic melt upon magma degassing. Starting materials were synthetic glasses with a composition close to a Krakatau dacitic andesite. The glasses contained 4.55–7.95 wt% H 2 O, ∼140 to 2700 ppm sulfur (S), and 0–1000 ppm chlorine (Cl). The experiments were carried out in internally heated pressure vessels (IHPV) at 1030 °C and oxygen fugacities ( f O 2 ) ranging from QFM+0.8 log units up to QFM+4.2 log units (QFM: quartz–fayalite–magnetite buffer). The decompression experiments were conducted by releasing pressure ( P ) continuously from ∼400 MPa to final P of 150, 100, 70 and 30 MPa. The decompression rate ( r ) ranged from 0.01 to 0.17 MPa/s. The samples were annealed for 0–72 h (annealing time, t A ) at the final P and quenched rapidly from 1030 °C to room temperature ( T ). The decompression led to the formation of a S-bearing aqueous fluid phase due to the relatively large fluid–melt partitioning coefficients of S. Secondary ion mass spectrometry (SIMS) was used to determine the isotopic composition of the glasses before and after decompression. Mass balance calculations were applied to estimate the gas–melt S isotope fractionation factor α g-m . No detectable effect of r and t A on α g-m was observed. However, SIMS data revealed a remarkable increase of α g-m from ∼0.9985 ± 0.0007 at >QFM+3 to ∼1.0042 ± 0.0042 at ∼QFM+1. Noteworthy, the isotopic fractionation at reducing conditions was about an order of magnitude larger than predicted by previous works. Based on our experimental results and on previous findings for S speciation in fluid and silicate melt a new model predicting the effect of f O 2 on α g-m (or Δ 34 S g–m ) in andesitic systems at 1030 °C is proposed. Our experimental results as well as our modeling are of high importance for the interpretation of S isotope signatures in natural samples (e.g., melt inclusions or volcanic gases).

Geochimica et Cosmochimica Acta↗

USGS2013

Evidence for microbial carbon and sulfur cycling in deeply buried ridge flank basalt

Sediment-covered basalt on the flanks of mid-ocean ridges constitutes most of Earth's oceanic crust, but the composition and metabolic function of its microbial ecosystem are largely unknown. By drilling into 3.5-million-year-old subseafloor basalt, we demonstrated the presence of methane- and sulfur-cycling microbes on the eastern flank of the Juan de Fuca Ridge. Depth horizons with functional genes indicative of methane-cycling and sulfate-reducing microorganisms are enriched in solid-phase sulfur and total organic carbon, host δ 13 C- and δ 34 S-isotopic values with a biological imprint, and show clear signs of microbial activity when incubated in the laboratory. Downcore changes in carbon and sulfur cycling show discrete geochemical intervals with chemoautotrophic δ 13 C signatures locally attenuated by heterotrophic metabolism.

Science↗