Figure 10 - uploaded by Peter Schlosser
Content may be subject to copyright.
Electron microscope picture of an interplanetary dust particle. The size of the particles carrying the extraterrestrial 3 He that are accumulated in marine sediments typically is between 3 and 35 μ m (e.g., Farley et al. 1997) [photo- graph courtesy of Scott Messenger, ]. 

Electron microscope picture of an interplanetary dust particle. The size of the particles carrying the extraterrestrial 3 He that are accumulated in marine sediments typically is between 3 and 35 μ m (e.g., Farley et al. 1997) [photo- graph courtesy of Scott Messenger, ]. 

Source publication
Article
Full-text available
Noble gases are widely used in studies of the basic properties and dynamics of natural systems including the ocean. This chapter describes some of the more extensive applications of noble gases (mainly helium isotopes) to studies of oceanographic problems. They include the modern oceanic circulation, paleo-oceanography, hydrothermal and cold brine...

Context in source publication

Context 1
... values of 1.3±0.5 × 10 6 and 3.1±1.2 × 10 6 atoms cm -2 s -1 , respectively. These values are comparable to the fluxes estimated for the continental crust (2.7±1 × 10 6 atoms cm -2 s -1 normalized to the continental area; e.g., Torgersen 1989). This shows that on a local/regional basis there are significant radiogenic 4 He fluxes from the ocean sediment into the water column. Such features are not unexpected because at certain locations the seafloor is closer to the composition of continental crust than oceanic crust. However, averaged over the entire ocean basins, the flux of crustal 4 He is small compared to that from the continental crust. Well et al. (2001) evaluated high-quality data from the Pacific Ocean that became available during the World Ocean Circulation Experiment (WOCE). Separating the crustal 4 He component from the mantle component, they revealed widespread occurrence of a crustal radiogenic 4 He flux out of deep-sea sediments and the oceanic crust into the water column (Fig. 9). Although the flux of 4 He is small in these regions, Well et al. (2001) were able to estimate a flux of roughly 1±0.4 × 10 5 atoms cm -2 s -1 . Further evaluation of the WOCE helium isotope and neon data will hopefully improve our knowledge on the distribution of helium sources and their relative flux values in the global ocean. After the discovery of mantle-derived helium in the oceans (Clarke et al. 1969), the first estimate of the 3 He flux yielded a value of about 2 atoms cm -2 s -1 (Clarke et al. 1969). This estimate was based on simple advection/diffusion or straight advection models that utilize the mean concentration of excess 3 He in the deep waters of the ocean ( ∆ 3 He) and mean residence time of the deep waters. The flux of this mantle-derived helium is concentrated in areas of active mid-ocean ridge spreading or ocean islands (e.g., Craig and Lupton 1981). Later estimates by Craig et al. (1975) were based on a larger, although still sparse, data set. In their new assessment of the 3 He flux from the ocean, these authors use two methods: one based on the average mean upwelling rate and the mean 3 He excess in the deep ocean, the other based on the 4 He flux and the 3 He/ 4 He ratio of the excess helium calculated from profiles located on the East Pacific Rise. They obtain values of 3.3 atoms cm -2 s -1 and 4.8 atoms cm -2 s -1 , respectively (average value given by Craig et al. 1975: 4±1 atoms cm -2 s -1 . Since these estimates of 3 He fluxes in the mid-1970s, little work has been done that would have resulted in significant refinements of these fluxes. Simulations of the mantle helium distribution using a global general ocean circulation model (Farley et al. 1995) used a simple parameterization of the 3 He flux from mid-ocean ridges and determined the distribution of the He emanated from these sources throughout the world ocean. These simulations showed that with the specific source parameterization used in their study, Farley et al. (1995) could reproduce the global oceanic balance of 3 He reasonably well. However, at the same time the simulations clearly revealed that there is still much work to be done to understand the details of the simulated fields. Comparison with high-density surveys of 3 He in the ocean that are now becoming available (e.g., Lupton 1998, Rüth et al 2000) will enable us to reach a deeper level of understanding of the 3 He patterns observed in the ocean. Such progress should make new efforts to refine the estimate of the oceanic 3 He flux a worthwhile exercise. Four decades ago, He of apparent extraterrestrial origin was identified in ocean sediments. Merrihue (1964) observed 3 He/ 4 He ratios in marine sediments roughly 2 orders of magnitude higher than those observed in atmospheric helium and attributed it to the presence of cosmic material. Systematic studies of noble gases in marine sediments were started in the early 1980s by Ozima et al. (1984). Shortly thereafter, Takayanagi and Ozima (1987) recognized the potential of 3 He as a proxy of sediment accumulation rates. Most studies of noble gases in marine sediments (including this chapter) focus on helium isotopes, however, neon (Nier and Schlutter 1990, 1993) and argon isotopes (Tilles 1966, 1967; Amari and Ozima 1988) have also been studied. In the early 1990s, extraterrestrial 3 He in ocean sediments received considerable attention when Anderson (1993) questioned the understanding of mantle geochemistry and proposed that the mantle 3 He might not represent volatiles trapped in the earth in early earth history but rather is derived from subducted interplanetary dust particles (IDPs). However, this hypothesis could be refuted based on mass flux considerations (Allègre et al. 1993) and experimental evidence showing that helium would not be retained during subduction due to sufficiently high diffusion coefficients (Hiyagon 1994). Extraterrestrial He is delivered to the earth surface by interplanetary dust particles (IDP, Fig. 10). IDPs are derived from asteroid collisions as well as cometary debris (Dohnanyi 1976) and are thought to acquire their characteristic helium signature from implantation of solar wind and solar flare gases (e.g., Nier and Schlutter 1990). Approximately 40,000 tons of IDPs are deposited annually on the earth’s surface (Love and Brownlee 1993). However, the major fraction of the IDPs is heated to temperatures >800°C during entry into the earth’s atmosphere and looses its helium signal (Farley et al. 1997). Only IDPs with diameters ≤ 35 microns, corresponding to 0.5% of the total IDP mass flux, transit the atmosphere at temperatures of 500-800°C or below (Fraundorf et al. 1982) and retain their extraterrestrial helium signature. After being removed from the troposphere mainly by wet deposition and rapid settling through the oceanic water column, the IDPs continuously accumulate in marine sediments (e.g., Takayanagi and Ozima 1987) or on ice shields (Brook et al. 2000). The helium isotope characteristics of IDPs are well constrained from analysis of individual particles collected from the stratosphere. They have a 3 He/ 4 He ratio of 2.4 × 10 -4 , as well as a fairly constant 3 He concentration of 1.9 × 10 -5 cm 3 STP g -1 (Nier and Schlutter 1992). As the cosmic dust is enriched in 3 He by ~8 orders of magnitude compared to terrigenous matter it can be readily detected. However, in spite of various noble gas studies of single IDP grains, both from the stratosphere and ocean sediments (e.g., Fukumoto et al. 1986; Nier et al. 1990; Nier and Schlutter 1992) the carrier phase that actually hosts the extraterrestrial helium has not been unambiguously identified. Amari and Ozima (1985) found that the helium resides mainly in the magnetic fraction of sediments and therefore identified magnetite to be the main carrier of the extraterrestrial 3 He signal. The magnetite is thought to be produced by heating of the IDPs during atmospheric entry (Amari and Ozima 1985). In a subsequent study, Fukumoto et al. (1986) found significant helium contributions from a non-magnetic fraction and suggested extraterrestrial silicates to be another likely host mineral. The presence of a non-magnetic carrier phase was later confirmed by Patterson et al. (1998) and Farley (2001). Future work is needed to identify the relative importance of different carrier phases and whether they are associated to magnetic and/or non-magnetic sediment fractions. The extraterrestrial helium signal is extremely well preserved in marine and terrestrial sedimentary archives over geological time scales. Various studies have shown that the extraterrestrial helium carried to the seafloor by IDPs can be retained for periods of at least 65 million years (Ma) against diffusive and/or diagenetic loss (Farley 1995; Farley et al. 1998). Recently, Patterson et al. (1998) identified extraterrestrial 3 He in 480- Ma old sedimentary rocks. Helium contained in ocean sediments can be interpreted as a mixture of helium from two sources, extraterrestrial and terrigeneous helium (Takayanagi and Ozima 1987; Marcantonio et al. 1995). Contributions from an atmospheric helium component have been shown to be negligible (e.g., Farley and Patterson 1995). Assuming that the isotopic compositions of both mixing end-members are known, one can easily calculate the amount of extraterrestrial 3 He, using the following ...

Citations

... [60] The decay of tritium ( 3 H, T 1/2 = 12.3 a) to 3 He allows to study ocean circulation. [60,61] Most of the tritium in the contemporary oceans derives from the atmospheric nuclear bomb tests in the 1960s. At the ocean surface, He efficiently exchanges with the atmosphere, but once a water parcel is decoupled from the atmosphere, the freshly produced tritiogenic 3 He will lead to an increase of the 3 He/ 4 He ratio above the atmospheric value. ...
Article
Full-text available
Noble gases are very rare elements in most relevant samples in geochemistry and cosmochemistry. Noble gases may perhaps also look rather boring to chemists, as they do not form any stable compounds. However, it is just their rarity and chemical inertness which makes noble gases versatile elements in a very wide range of fields, such as oceanography, climatology, environmental sciences, meteorite studies, rock dating, early solar system and early Earth history, and many others. Mass spectrometry is by far the main analytical tool in noble gas geochemistry and cosmochemistry, partly because the rarity of noble gases often allows researchers to recognize in the same sample different noble gas "components" of different origin and hence different isotopic composition. This contribution attempts to illustrate the wide range of applications of noble gas mass spectrometry in the Earth sciences with selected examples.
... Analysis of dissolved gases in water is common in oceanographic and terrestrial hydrologic studies. Various combinations of dissolved gases can provide records of environmental change and a deeper understanding of groundwater flow systems (Heaton and Vogel, 1981;Heaton and others, 1983;Stute and others, 1995;Aeschbach-Hertig and others, 1999;Ballentine and Hall, 1999;Cey and others, 2008;Cartwright and others, 2017), groundwater discharges to surface water (Heilweil and others, 2015;Sanford and others, 2015;Gilmore and others, 2016), ocean circulation patterns and mixing (Schlosser and Winckler, 2002;Stanley and Jenkins, 2013;Loose and Jenkins, 2014), and emission rates of greenhouse gases from parts of the hydrosphere (Matthews and Fung, 1987;Dalal and Allen, 2008;Jeffrey and others, 2018). ...
Technical Report
Full-text available
DGMETA (Dissolved Gas Modeling and Environmental Tracer Analysis) is a Microsoft Excel-based computer program that is used for modeling air-water equilibrium conditions from measurements of dissolved gases and for computing concentrations of environmental tracers that rely on air-water equilibrium model results. DGMETA can solve for the temperature, salinity, excess air, fractionation of gases, or pressure/elevation of water when it is equilibrated with the atmosphere. Models are calibrated inversely using one or more measurements of dissolved gases such as helium, neon, argon, krypton, xenon, and nitrogen. Excess nitrogen gas, originating from denitrification or other sources, also can be included as a fitted parameter or as a separate calculation from the dissolved gas modeling results. DGMETA uses the air-water equilibrium models to separate measured concentrations of gases and isotopes of gases into components that are used for tracing water in the environment. DGMETA calculates atmospheric dry-air mole fractions (mixing ratios) for transient atmospheric gas tracers such as chlorofluorocarbons, sulfur hexafluoride, and bromotrifluoromethane (Halon-1301); and concentrations of tritiogenic helium-3 and radiogenic helium-4, which accumulate from the decay of tritium in water and the decay of uranium and thorium in rocks, respectively. Sample data can be graphed to identify applicable models of excess air, samples that contain excess nitrogen gas, or samples that have partially degassed, for example. Monte Carlo analysis of errors associated with dissolved gas equilibrium model results can be carried through computations of environmental tracer concentrations to provide robust estimates of error. In addition, graphical routines for separating helium sources using helium isotopes are included to refine estimates of tritiogenic helium-3 when terrigenic helium from mantle or crustal sources is present in samples. Environmental tracer concentrations and their errors computed from DGMETA can be used with other programs, such as TracerLPM (Jurgens and others, 2012), to determine groundwater ages and biogeochemical reaction rates. DGMETA also produces output files in a format that meets the U.S. Geological Survey open data requirements for documentation of model inputs and outputs. DGMETA is a versatile and adaptable program that allows users to add solubility data for new gases, modify the existing set of gas solubility data, modify the default set of gases used for modeling, choose calculations based on real (non-ideal) gas behavior, and select various concentration units for data entry and results to match laboratory reports and study objectives. DGMETA comes with a set of gases widely used in hydrology and oceanography and many gases include multiple solubilities from previous work. Seventeen dissolved gases are included in the default version of the program: noble gases (helium, neon, argon, krypton, and xenon), reactive gases (nitrogen, oxygen, methane, carbon dioxide, carbon monoxide, hydrogen, and nitrous oxide), and environmental tracers (chlorofluorocarbon-11, chlorofluorocarbon-12, chlorofluorocarbon-113, sulfur hexafluoride, and Halon-1301).
... Constant flux proxies are geochemical parameters with well-constrained and stable source functions, such as 230 Th (Bacon, 1984;Francois et al., 2004) and 3 He (Marcantonio et al., 1996;McGee & Mukhopadhyay, 2013;Schlosser & Winckler, 2002;Winckler et al., 2004). 230 Th is produced by the steady decay of uranium dissolved in seawater, after which it is rapidly removed by sinking particles and buried on the seafloor (see section 2) (Bacon, 1984;Francois et al., 1990;Francois et al., 2004;Suman & Bacon, 1989). ...
Article
Full-text available
Th normalization is a valuable paleoceanographic tool for reconstructing high‐resolution sediment fluxes during the late Pleistocene (last ~500,000 years). As its application has expanded to ever more diverse marine environments, the nuances of ²³⁰Th systematics, with regard to particle type, particle size, lateral advective/diffusive redistribution, and other processes, have emerged. We synthesized over 1000 sedimentary records of ²³⁰Th from across the global ocean at two time slices, the late Holocene (0–5,000 years ago, or 0–5 ka) and the Last Glacial Maximum (18.5–23.5 ka), and investigated the spatial structure of ²³⁰Th‐normalized mass fluxes. On a global scale, sedimentary mass fluxes were significantly higher during the Last Glacial Maximum (1.79–2.17 g/cm²kyr, 95% confidence) relative to the Holocene (1.48–1.68 g/cm²kyr, 95% confidence). We then examined the potential confounding influences of boundary scavenging, nepheloid layers, hydrothermal scavenging, size‐dependent sediment fractionation, and carbonate dissolution on the efficacy of ²³⁰Th as a constant flux proxy. Anomalous ²³⁰Th behavior is sometimes observed proximal to hydrothermal ridges and in continental margins where high particle fluxes and steep continental slopes can lead to the combined effects of boundary scavenging and nepheloid interference. Notwithstanding these limitations, we found that ²³⁰Th normalization is a robust tool for determining sediment mass accumulation rates in the majority of pelagic marine settings (>1,000 m water depth).
... Furthermore, 4 He concentrations of the nodules are much higher than those of the crusts ( Table 2). According to the principle of mass conservation, Suess and Wanke [1] speculated that U and Th in the pelagic sediments would decay to produce 4 He-rich sediment pore-water and there would be significant radioactive 4 He flux from the deep-sea sediments into the ambient seawater [74]. The nodules are directly grown or buried under the surface of sediments, whose 4 He may be influenced by the combined effects of terrestrial substances and the 4 He-rich sediment pore-water, which are featured by their high 4 He abundances. ...
... The 3 He/ 4 He ratios of the SCS crusts/nodules (except HYD66-1) range from 0.25 to 0.67 RA where the He in these samples represents a mixture between radiogenic crustal He (0.01-0.05 RA) and air-saturated seawater (<1 RA). Although atmospheric He contribution to deep-sea sediments may be negligible [19,74], the He trapped in the Fe-Mn crusts and nodules cannot be neglected because the Mn-Fe oxide/hydroxide colloid are formed directly in the ambient seawater. However, Ar is more soluble in seawater than He, hence seawater has the same Ar isotope compositions as the atmosphere and deep-sea sediments often inherit the Ar isotopes of seawater [47]. ...
... Furthermore, 4 He concentrations of the nodules are much higher than those of the crusts (Table 2). According to the principle of mass conservation, Suess and Wanke [1] speculated that U and Th in the pelagic sediments would decay to produce 4 He-rich sediment pore-water and there would be significant radioactive 4 He flux from the deep-sea sediments into the ambient seawater [74]. The nodules are directly grown or buried under the surface of sediments, whose 4 He may be influenced by the combined effects of terrestrial substances and the 4 He-rich sediment pore-water, which are featured by their high 4 He abundances. ...
Article
Full-text available
In this study, the He and Ar isotope compositions were measured for the Fe-Mn polymetallic crusts and nodules from the South China Sea (SCS), using the high temperature bulk melting method and noble gases isotope mass spectrometry. The He and Ar of the SCS crusts/nodules exist mainly in the Fe-Mn mineral crystal lattice and terrigenous clastic mineral particles. The results show that the 3He concentrations and R/RA values of the SCS crusts are generally higher than those of the SCS nodules, while 4He and 40Ar concentrations of the SCS crusts are lower than those of the SCS nodules. Comparison with the Pacific crusts and nodules, the SCS Fe-Mn crusts/nodules have lower 3He concentrations and 3He/4He ratios (R/RA, 0.19 to 1.08) than those of the Pacific Fe-Mn crusts/nodules, while the 40Ar/36Ar ratios of the SCS samples are significantly higher than those of the Pacific counterparts. The relatively low 3He/4He ratios and high 40Ar concentrations in the SCS samples are likely caused by terrigenous detrital input with high radiogenic 4He and 40Ar contents. The SCS crusts and nodules have shorter growth periods, implying that in situ post-formation radiogenic 3He, 4He and 40Ar produced by decay of U, Th and K have no effect on their isotope compositions. Thus, the SCS crusts/nodules inherited the noble gases characteristics of their sources. Helium and Ar isotope compositions in the SCS Fe-Mn crusts and nodules reflect the product of an equilibrium mixture between air-saturated seawater and radiogenic components during their growth, while the partial 3He excess in some SCS samples may represent a little mantle-derived origin. The different He and Ar isotope compositions of the Fe-Mn crusts and nodules between the South China Sea and the Pacific Ocean are due to their different sources and genetic processes. The characteristics of He and Ar isotope compositions in the SCS polymetallic crusts and nodules are similar to the properties of hydrogenetic Fe-Mn oxide/hydroxide precipitates, which reflects mainly the product of an equilibrium mixture between air-saturated seawater and radiogenic components.
... The latter provides information about the age and extent of recent surface water incursion (Schlosser and Winckler 2002;Stanley and Jenkins 2013). ...
... At the ocean surface, helium is essentially in solubility equilibrium with the atmosphere. However, at depth, several important processes alter the isotopic ratio ( Fig. 1 -see Schlosser and Winckler, 2002, for a review). Firstly, 3 He is produced by the radioactive decay of tritium , and secondly, terrigenic helium is introduced not only by the release of helium from submarine volcanic activity at mid-ocean ridges and volcanic centres, with ele- (Lupton et al., 1977a, b;Jenkins et al., 1978;Lupton, 1979;Craig and Lupton, 1981;Jean-Baptiste et al., 1991a, 1992, but also by the addition of helium with a low 3 He / 4 He ratio from the crust and sedimentary cover, mostly due to α-decay of uranium and thorium minerals (Craig and Weiss, 1971). ...
Thesis
Full-text available
Dans cette thèse nous avons simulé la distribution d’éléments traces en Méditerranée, dans le but de mieux contraindre la circulation thermohaline et les cycles biogéochimiques. Pour cela, nous avons utilisé le modèle dynamique à haute résolution NEMO-MED12 couplé avec le modèle de biogéochimie marine PISCES.La Méditerranée offre un cadre particulièrement attrayant pour l’étude des traceurs géochimiques. Il s’agit d’une mer semi-fermée, ce qui permet de mieux contraindre les différentes sources et puits des éléments (poussières atmosphériques, fleuves …). Plus particulièrement, nous avons modélisé le tritium (3H), traceur transitoire couramment utilisé pour l’étude de la variabilité interannuelle de la circulation thermohaline. Nous avons aussi simulé les isotopes de l’hélium (3He, 4He), traceurs conservatifs injectés par l’activité volcanique sous-marine et les sédiments, pour contraindre la circulation profonde. Nous nous sommes intéressés également à la composition isotopique du Néodyme (Nd), traceur permettant d’étudier les échanges de matière avec les marges continentales, ainsi qu’à la modélisation du radiocarbone (14C), qui permet d’avoir des informations uniques sur les variations de la circulation thermohaline et des processus de mélange sur les périodes récentes et passées.Cette ensemble de simulations nouvelles et la confrontation avec des observations récentes d’éléments traces issues de différents programmes d’observation (GEOTRACES, METEOR, PALEOMEX), a apporté une expertise nouvelle et supplémentaire sur la dynamique et les cycles biogéochimique en mer Méditerranée. Ce travail contribue à améliorer le modèle régional NEMO/Med12/PISCES développé pour ce bassin, apporte une expertise essentielle pour développer notre aptitude à prévoir l’évolution future de ce bassin sous la pression du changement anthropique.
... At the ocean surface, helium is essentially in solubility equilibrium with the atmosphere. However, at depth, several important processes alter the isotopic ratio ( Fig. 1 -see Schlosser and Winckler, 2002, for a review). Firstly, 3 He is produced by the radioactive decay of tritium , and secondly, terrigenic helium is introduced not only by the release of helium from submarine volcanic activity at mid-ocean ridges and volcanic centres, with ele- 3 He / 4 He ratios typical of their mantle source (Lupton et al., 1977a, b;Jenkins et al., 1978;Lupton, 1979;Craig and Lupton, 1981;Jean-Baptiste et al., 1991a, 1992, but also by the addition of helium with a low 3 He / 4 He ratio from the crust and sedimentary cover, mostly due to α-decay of uranium and thorium minerals (Craig and Weiss, 1971). ...
Article
Full-text available
Helium isotopes (3He, 4He) are useful tracers for investigating the deep ocean circulation and for evaluating ocean general circulation models, because helium is a stable and conservative nuclide that does not take part in any chemical or biological process. Helium in the ocean originates from three different sources, namely, (i) gas dissolution in equilibrium with atmospheric helium, (ii) helium-3 addition by radioactive decay of tritium (called tritiugenic helium), and (iii) injection of terrigenic helium-3 and helium-4 by the submarine volcanic activity which occurs mainly at plate boundaries, and also addition of (mainly) helium-4 from the crust and sedimentary cover by α-decay of uranium and thorium contained in various minerals. We present the first simulation of the terrigenic helium isotope distribution in the whole Mediterranean Sea using a high-resolution model (NEMO-MED12). For this simulation we build a simple source function for terrigenic helium isotopes based on published estimates of terrestrial helium fluxes. We estimate a hydrothermal flux of 3.5 mol3 He yr−1 and a lower limit for the crustal flux at 1.6 × 10−7 4He mol m−2 yr−1. In addition to providing constraints on helium isotope degassing fluxes in the Mediterranean, our simulations provide information on the ventilation of the deep Mediterranean waters which is useful for assessing NEMO-MED12 performance. This study is part of the work carried out to assess the robustness of the NEMO-MED12 model, which will be used to study the evolution of the climate and its effect on the biogeochemical cycles in the Mediterranean Sea, and to improve our ability to predict the future evolution of the Mediterranean Sea under the increasing anthropogenic pressure.
... studies of hydrothermal fluids from mid-ocean ridges, which often have a He isotopic composition representing a mixture between air and upper mantle (e.g. Schlosser and Winckler, 2002) resulting from the uptake of He from the oceanic crust by the hydrothermal fluid. Undoubtedly, these fluid-rock interaction processes do not only change the He concentration and composition of the oceanic crust and the hydrothermal fluid but also its heavier noble gas inventory. ...
... The NMORB and seawater Cl concentrations (20 and 19,400 ppm) were taken from Quinby-Hunt and Turekian (1983) and Wallace and Anderson (2000), respectively. The composition of the brine phase was taken from Kent et al. (1999) and Schlosser and Winckler (2002). 2r uncertainties are shown where larger than symbol. ...
... The stippled lines represent mixing models between altered oceanic crust (AC) and mantle melts. The altered oceanic crust used in these models represents average oceanic crust (OC) mixed with different amounts of seawater (AC1 = OC + 0.5% SW; AC2 = OC + 1.25% SW) and a brine phase (AC3 = OC + 1.15% brine, the composition of the brine phase was taken from Schlosser and Winckler (2002)). 2r uncertainties are shown where larger than symbol. ...
Article
Both, terrestrial and extra-terrestrial applications of noble gases have demonstrated their importance as tracers for source identification, process characterisation and mass and heat flux quantification. However, the interpretation of noble gas isotope data from terrestrial igneous rocks is often complicated by the ubiquitous presence of heavy noble gases (Ne, Ar, Kr, Xe) with an atmospheric origin. Up to now there has been no consensus on how atmospheric noble gases are entrained into igneous rocks. Suggested processes range from contamination during sample preparation to mantle recycling through subduction. Here we present Ne, Ar, Mg, K, and Cl data of fresh glasses from the Mid-Atlantic Ridge north and south of the Ascension Fracture Zone which show that incorporation of atmospheric noble gases into igneous rocks is in general a two-step process: (1) magma contamination by assimilation of altered oceanic crust results in the entrainment of noble gases from air-equilibrated seawater; (2) atmospheric noble gases are adsorbed onto grain surfaces during sample preparation. This implies, considering the ubiquitous presence of the contamination signal, that magma contamination by assimilation of a seawater-sourced component is an integral part of mid-ocean ridge basalt evolution. Combining the results obtained from noble gas and Cl/K data with estimates of crystallisation pressures for the sample suite shows that the magma contamination must have taken place at a depth between 9 and 13. km. Taking thickness estimates for the local oceanic crust into account, this implies that seawater penetration in this area reaches lower crustal levels, indicating that hydrothermal circulation might be an effective cooling mechanism even for the deep parts of the oceanic crust.
... In the last few decades, noble gases in aquatic systems have become a well-established geochemical tool for investigating physical transport and exchange processes in lakes, oceans, and ground waters and for reconstructing past climate conditions (for reviews see Kipfer et al., 2002;Schlosser and Winckler, 2002;Aeschbach-Hertig and Solomon, 2013;Brennwald et al., 2013;Stanley and Jenkins, 2013). ...
... The atmospheric noble gases He, Ne, Ar, Kr, and Xe are widely used as tracers to analyze the dynamics of aquatic systems such as lakes, oceans, and groundwaters [1,2]. Recently, new methods have been developed to determine noble-gas concentrations in the porewater of bulk samples of unconsolidated sediment that include both liquid and solid phases (i.e., both porewater and sediment matrix) [3,4]. ...
Article
Full-text available
Although the naturally occurring atmospheric noble gases He, Ne, Ar, Kr, and Xe possess great potential as tracers for studying gas exchange in living beings, no direct analytical technique exists for simultaneously determining the absolute concentrations of these noble gases in body fluids in vivo. In this study, using human blood as an example, the absolute concentrations of all stable atmospheric noble gases were measured simultaneously by combining and adapting two analytical methods recently developed for geochemical research purposes. The partition coefficients determined between blood and air, and between blood plasma and red blood cells, agree with values from the literature. While the noble-gas concentrations in the plasma agree rather well with the expected solubility equilibrium concentrations for air-saturated water, the red blood cells are characterized by a distinct supersaturation pattern, in which the gas excess increases in proportion to the atomic mass of the noble-gas species, indicating adsorption on to the red blood cells. This study shows that the absolute concentrations of noble gases in body fluids can be easily measured using geochemical techniques that rely only on standard materials and equipment, and for which the underlying concepts are already well established in the field of noble-gas geochemistry.