Search USGS⌕ Search

USGS · 70035560

A new syringe pump apparatus for the retrieval and temporal analysis of helium in groundwaters and geothermal fluids

Abstract

We present details of a newly designed syringe pump apparatus for the retrieval and temporal analysis of helium (SPARTAH). The device is composed of a commercially available syringe pump connected to coils of Cu tubing, which interface the syringe and the groundwater or geothermal wellhead. Through test deployments at geothermal wells in Iceland and California, we show that well fluids are drawn smoothly, accurately, and continuously into the Cu tubing and can be time‐stamped through user‐determined operating parameters. In the laboratory, the tubing is sectioned to reveal helium (He) characteristics of the fluids at times and for durations of interest. The device is capable of prolonged deployments, up to 6 months or more, with minimal maintenance. It can be used to produce detailed time series records of He, or any other geochemical parameter, in groundwaters and geothermal fluids. SPARTAH has application in monitoring projects assessing the relationship between external transient events (e.g., earthquakes) and geochemical signals in aqueous fluids.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

P.H. Barry, David R. Hilton, M.D. Tryon, K. M. Brown, J.T. Kulongoski. 2009-05-09. A new syringe pump apparatus for the retrieval and temporal analysis of helium in groundwaters and geothermal fluids. https://doi.org/10.1029/2009gc002422

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related USGS reports

Erupted volume during the 2014–2023 Semisopochnoi unrest and eruption constrained by multi-platform InSAR and volcanic gas observations

Volcano deformation data provide important constraints on magma dynamics during volcanic unrest and eruptions. From these observations, we can estimate subsurface pressure changes and relate them to volume change in the reservoir. However, because magma and rock are compressible, this volume change cannot be directly equated with eruptive volume. When we combine geodetic analyses with gas observations, petrologic constraints, volatile solubility modeling, and magma compressibility equations, however, we can estimate realistic lower and upper bounds of eruptive volume. Leveraging multi‐platform InSAR time series and satellite SO 2 data, we apply these methods to the 2014–2023 unrest and eruption of Semisopochnoi, Alaska. We find that this phreatomagmatic eruption sequence was fed by a spherical magma source at 6.5–7.5 km depth bsl, centered beneath the caldera, ∼5 km offset to the east from the vent. Volatile solubility modeling indicates that ∼50% of the initial dissolved CO 2 has exsolved at depths consistent with the geodetic source depth, increasing the magma compressibility. Combining geodetic model constraints with SO 2 observations, petrologic constraints, solubility models, and magma compressibility findings yields 12–32 Mm 3 as the most‐likely juvenile, dense‐rock equivalent eruptive volume, with a best estimate of 20 Mm 3 . Stress change modeling suggests that the local stress field encouraged conduit formation west of the pre‐eruptive inflation center, and that the 2014 M7.9 Rat Island earthquake, ∼65 km to the west of Semisopochnoi, reduced the compressive stress underneath the volcano, supporting prolonged eruptive activity.

Alaska↗

Pre-eruptive volatiles and magma storage depth for the 2018 eruption at Mount Veniaminof, Alaska

Mount Veniaminof is a frequently active, open-system arc volcano on the Alaska Peninsula, part of the Alaska-Aleutian arc. Mount Veniaminof's September–December 2018 eruption began with small lava flows and culminated in a larger explosive event in November that produced a 450 km long continuous ash plume—one of the volcano's most significant ash-producing events in recently observed eruptions. A temporally constrained tephra record was sampled after the eruption. We present volatile element concentrations (H, C, S, Cl, F) from a total of 65 olivine-hosted melt inclusions (MIs) across six tephra layers to assess potential variations in magma chemistry throughout the course of the eruption. No variation is observed in volatile concentrations across the tephra layers, and there is no correlation between volatile concentrations and the explosivity of eruptive pulses leading to the November explosive event. H 2 O concentrations within MI suggest moderately hydrous magmas up to 2.4 wt% H 2 O and a large range in CO 2 concentrations in the MI (14–2,180 ppm) from Secondary Ion Mass Spectrometry and vapor bubble reconstructions. H 2 O and CO 2 measurements correspond to entrapment pressures up to 400 MPa (entrapment depths ∼15 km), but with modal storage around 100–200 MPa. H 2 O contents can be reconciled with previous microlite number density estimates using a polybaric storage history.

Alaska↗

Hydrothermal manganese-oxide mineralization of a carbonate ooze, Samoan hotspot region, South Pacific Ocean

Low-temperature hydrothermal manganese oxides occur throughout the global oceans. However, the hydrothermal replacement of a carbonate ooze by manganese oxides is described here for the first time. The 24 samples dredged from three locations around the Territory of American Samoa in the South Pacific Ocean include six samples with remnant carbonate and volcaniclastic sediments, which we refer to as “low Mn,” and 18 samples in which the mineralization is pervasive and has replaced most original sediment, termed “high Mn.” The 18 high-Mn samples exhibit a mean Mn content of 51 wt.%. Higher Li and Mn contents and lower Fe contents in the high-Mn samples indicate a hydrothermal origin and distinguish these samples from hydrogenetic ferromanganese crusts. Mn-oxide layers are up to 90 mm thick, some with columns to 44 mm long and 10 mm wide, the magnitude of which has not been described previously. Samples are composed of birnessite and 10 Å phyllomanganate minerals. Textures of the thickest Mn layers indicate mineralization below the seabed from ascending fluids during multiple hydrothermal pulses. Mineralization took place by complete to partial replacement and cementation of foraminiferal sediments intermixed with volcaniclastic sediments in varying amounts. Our results highlight the production of carbonate sediment-hosted hydrothermal Mn oxides from multiple hydrothermal sources within the Samoan volcanic chain. The potential extensive distribution on the regional scale of this newly described mineralization process and unique element enrichments raise questions about its broader distribution globally and potential importance to hydrothermal processes, element mass balance, and seabed mineral resources.

Geochemistry, Geophysics, Geosystems↗