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Featured researches published by Ate Visser.


Water Resources Research | 2013

Groundwater age distributions at a public drinking water supply well field derived from multiple age tracers (85Kr, 3H/3He, and 39Ar)

Ate Visser; Hans Peter Broers; Roland Purtschert; Jürgen Sültenfuß; Martin de Jonge

[1]xa0Groundwater age is a key aspect of production well vulnerability. Public drinking water supply wells typically have long screens and are expected to produce a mixture of groundwater ages. The groundwater age distributions of seven production wells of the Holten well field (Netherlands) were estimated from tritium-helium (3H/3He), krypton-85 (85Kr), and argon-39 (39Ar), using a new application of a discrete age distribution model and existing mathematical models, by minimizing the uncertainty-weighted squared differences of modeled and measured tracer concentrations. The observed tracer concentrations fitted well to a 4-bin discrete age distribution model or a dispersion model with a fraction of old groundwater. Our results show that more than 75% of the water pumped by four shallow production wells has a groundwater age of less than 20 years and these wells are very vulnerable to recent surface contamination. More than 50% of the water pumped by three deep production wells is older than 60 years. 3H/3He samples from short screened monitoring wells surrounding the well field constrained the age stratification in the aquifer. The discrepancy between the age stratification with depth and the groundwater age distribution of the production wells showed that the well field preferentially pumps from the shallow part of the aquifer. The discrete groundwater age distribution model appears to be a suitable approach in settings where the shape of the age distribution cannot be assumed to follow a simple mathematical model, such as a production well field where wells compete for capture area.


Rapid Communications in Mass Spectrometry | 2013

A membrane inlet mass spectrometry system for noble gases at natural abundances in gas and water samples

Ate Visser; Michael J. Singleton; Darren J. Hillegonds; C. A. Velsko; Jean E. Moran; Bradley K. Esser

RATIONALEnNoble gases dissolved in groundwater can reveal paleotemperatures, recharge conditions, and precise travel times. The collection and analysis of noble gas samples are cumbersome, involving noble gas purification, cryogenic separation and static mass spectrometry. A quicker and more efficient sample analysis method is required for introduced tracer studies and laboratory experiments.nnnMETHODSnA Noble Gas Membrane Inlet Mass Spectrometry (NG-MIMS) system was developed to measure noble gases at natural abundances in gas and water samples. The NG-MIMS system consists of a membrane inlet, a dry-ice water trap, a carbon-dioxide trap, two getters, a gate valve, a turbomolecular pump and a quadrupole mass spectrometer equipped with an electron multiplier. Noble gases isotopes (4)He, (22)Ne, (38)Ar, (84)Kr and (132)Xe are measured every 10 s.nnnRESULTSnThe NG-MIMS system can reproduce measurements made on a traditional noble gas mass spectrometer system with precisions of 2%, 8%, 1%, 1% and 3% for He, Ne, Ar, Kr and Xe, respectively. Noble gas concentrations measured in an artificial recharge pond were used to monitor an introduced xenon tracer and to reconstruct temperature variations to within 2 °C. Additional experiments demonstrated the capability to measure noble gases in gas and in water samples, in real time.nnnCONCLUSIONSnThe NG-MIMS system is capable of providing analyses sufficiently accurate and precise for introduced noble gas tracers at managed aquifer recharge facilities, groundwater fingerprinting based on excess air and noble gas recharge temperature, and field and laboratory studies investigating ebullition and diffusive exchange.


Water Research | 2016

Geostatistical analysis of tritium, groundwater age and other noble gas derived parameters in California

Ate Visser; Jean E. Moran; Darren J. Hillegonds; Michael J. Singleton; Justin T. Kulongoski; Kenneth Belitz; Bradley K. Esser

Key characteristics of California groundwater systems related to aquifer vulnerability, sustainability, recharge locations and mechanisms, and anthropogenic impact on recharge are revealed in a spatial geostatistical analysis of a unique data set of tritium, noble gases and other isotopic analyses unprecedented in size at nearly 4000 samples. The correlation length of key groundwater residence time parameters varies between tens of kilometers ((3)H; age) to the order of a hundred kilometers ((4)Heter; (14)C; (3)Hetrit). The correlation length of parameters related to climate, topography and atmospheric processes is on the order of several hundred kilometers (recharge temperature; δ(18)O). Young groundwater ages that highlight regional recharge areas are located in the eastern San Joaquin Valley, in the southern Santa Clara Valley Basin, in the upper LA basin and along unlined canals carrying Colorado River water, showing that much of the recent recharge in central and southern California is dominated by river recharge and managed aquifer recharge. Modern groundwater is found in wells with the top open intervals below 60xa0m depth in the southeastern San Joaquin Valley, Santa Clara Valley and Los Angeles basin, as the result of intensive pumping and/or managed aquifer recharge operations.


Plant Cell and Environment | 2016

Dissolved atmospheric gas in xylem sap measured with membrane inlet mass spectrometry

H. Jochen Schenk; Susana Espino; Ate Visser; Bradley K. Esser

A new method is described for measuring dissolved gas concentrations in small volumes of xylem sap using membrane inlet mass spectrometry. The technique can be used to determine concentrations of atmospheric gases, such as argon, as reported here, or for any dissolved gases and their isotopes for a variety of applications, such as rapid detection of trace gases from groundwater only hours after they were taken up by trees and rooting depth estimation. Atmospheric gas content in xylem sap directly affects the conditions and mechanisms that allow for gas removal from xylem embolisms, because gas can dissolve into saturated or supersaturated sap only under gas pressure that is above atmospheric pressure. The method was tested for red trumpet vine, Distictis buccinatoria (Bignoniaceae), by measuring atmospheric gas concentrations in sap collected at times of minimum and maximum daily temperature and during temperature increase and decline. Mean argon concentration in xylem sap did not differ significantly from saturation levels for the temperature and pressure conditions at any time of collection, but more than 40% of all samples were supersaturated, especially during the warm parts of day. There was no significant diurnal pattern, due to high variability between samples.


Journal of Environmental Radioactivity | 2018

Analysis of air mass trajectories to explain observed variability of tritium in precipitation at the Southern Sierra Critical Zone Observatory, California, USA

Ate Visser; Melissa Thaw; Brad K. Esser

Understanding the behavior of tritium, a radioactive isotope of hydrogen, in the environment is important to evaluate the exposure risk of anthropogenic releases, and for its application as a tracer in hydrology and oceanography. To understand and predict the variability of tritium in precipitation, HYSPLIT air mass trajectories were analyzed for 16 aggregate precipitation samples collected over a 2 year period at irregular intervals at a research site located at 2000 m elevation in the southern Sierra Nevada (California, USA). Attributing the variation in tritium to specific source areas confirms the hypothesis that higher latitude or inland sources bring higher tritium levels in precipitation than precipitation originating in the lower latitude Pacific Ocean. In this case, the source of precipitation accounts for 79% of the variation observed in tritium concentrations. Air mass trajectory analysis is a promising tool to improve the predictions of tritium in precipitation at unmonitored locations and thoroughly understand the processes controlling transport of tritium in the environment.


Hydrological Processes | 2018

Importance of river water recharge to the San Joaquin Valley groundwater system

Ate Visser; Jean E. Moran; Michael J. Singleton; Bradley K. Esser

Nuclear and Chemical Sciences Division, Lawrence Livermore National Laboratory, Livermore, CA, USA Department of Earth & Environmental Sciences, California State University, East Bay, Hayward, CA, USA Correspondence Ate Visser, Nuclear and Chemical Sciences Division, Lawrence Livermore National Laboratory, P.O. Box 808, Livermore, CA 94551‐0808, USA. Email: [email protected] Funding information California State Water Resources Control Board; LLNL LDRD, Grant/Award Number: 15‐ERD‐042


Applied Geochemistry | 2014

A Bayesian Modeling Approach for Estimation of a Shape-Free Groundwater Age Distribution using Multiple Tracers

Arash Massoudieh; Ate Visser; Soroosh Sharifi; Hans Peter Broers


Applied Geochemistry | 2014

Intercomparison of tritium and noble gases analyses, 3H/3He ages and derived parameters excess air and recharge temperature

Ate Visser; E. Fourré; Florent Barbecot; Luc Aquilina; Thierry Labasque; Virginie Vergnaud; Bradley K. Esser


Journal of Hydrology | 2016

Nitrate vulnerability projections from Bayesian inference of multiple groundwater age tracers

Jamal Alikhani; Amanda Deinhart; Ate Visser; Richard K. Bibby; Roland Purtschert; Jean E. Moran; Arash Massoudieh; Bradley K. Esser


Journal of Hydrology | 2016

Distribution of tritium in precipitation and surface water in California

Patrick A. Harms; Ate Visser; Jean E. Moran; Brad K. Esser

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Bradley K. Esser

Lawrence Livermore National Laboratory

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Jean E. Moran

California State University

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Michael J. Singleton

Lawrence Livermore National Laboratory

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Richard K. Bibby

Lawrence Livermore National Laboratory

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Amanda Deinhart

Lawrence Livermore National Laboratory

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Arash Massoudieh

The Catholic University of America

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Brad K. Esser

Lawrence Livermore National Laboratory

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Darren J. Hillegonds

International Atomic Energy Agency

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