Revisiting Mt. Fuji's groundwater origins with helium, vanadium and eDNA tracers

Known locally as the water mountain , for millennia Japan's iconic Mt. Fuji has provided safe drinking water to millions of people via a vast network of groundwater and freshwater springs. Groundwater, which is recharged at high elevations, flows down Fuji's flanks within three basaltic aquifers, ultimately forming countless pristine freshwater springs along Fuji's foothills. Here, we challenge the current conceptual model of Fuji being a simple system of laminar groundwater flow with little to no vertical exchange between its three aquifers. This model contrasts strongly with Fuji's extreme tectonic instability due to its unique location on top of the only known continental trench-trench-trench triple junction, its complex geology, and its unusual microbial spring water communities. Based on a unique combination of microbial environmental DNA (eDNA), vanadium, and helium tracers, we provide evidence for prevailing deep circulation and previously unknown deep groundwater contribution to Fuji's freshwater springs. The most substantial deep groundwater upwelling has been found along Japan's tectonically most active Fujikawa-kako Fault Zone. Our findings broaden the hydrogeological understanding of Fuji and demonstrate the vast potential of combining eDNA, on-site noble gas, and trace element analyses for groundwater science

Inter-calibration of a proposed new primary reference standard AA-ETH Zn for zinc isotopic analysis

We have prepared a large volume of pure, concentrated and homogenous zinc standard solution. This new standard solution is intended to be used as a primary reference standard for the zinc isotope community, and to serve as a replacement for the nearly exhausted current reference standard, the so-called JMC-Lyon Zn. The isotopic composition of this new zinc standard (AA-ETH Zn) has been determined through an inter-laboratory calibration exercise, calibrated against the existing JMC-Lyon standard, as well as the certified Zn reference standard IRMM-3702. The data show that the new standard is isotopically indistinguishable from the IRMM-3702 zinc standard, with a weighted δ66/64Zn value of 0.28 ± 0.02‰ relative to JMC-Lyon. We suggest that this new standard be assigned a δ66/64Zn value of +0.28‰ for reporting of future Zn isotope data, with the rationale that all existing published Zn isotope data are presented relative to the JMC-Lyon standard. Therefore our proposed presentation allows for a direct comparison with all previously published data, and that are directly traceable to a certified reference standard, IRMM-3702 Zn. This standard will be made freely available to all interested labs through contact with the corresponding author

GEOTRACES IC1 (BATS) contamination-prone trace element isotopes Cd, Fe, Pb, Zn, Cu, and Mo intercalibration

International audienceWe report data on the isotopic composition of cadmium, copper, iron, lead, zinc, and molybdenum at the GEOTRACES IC1 BATS Atlantic intercalibration station. In general, the between lab and within-lab precisions are adequate to resolve global gradients and vertical gradients at this station for Cd, Fe, Pb, and Zn. Cd and Zn isotopes show clear variations in the upper water column and more subtle variations in the deep water; these variations are attributable, in part, to progressive mass fractionation of isotopes by Rayleigh distillation from biogenic uptake and/or adsorption. Fe isotope variability is attributed to heavier crustal dust and hydrothermal sources and light Fe from reducing sediments. Pb isotope variability results from temporal changes in anthropogenic source isotopic compositions and the relative contributions of U.S. and European Pb sources. Cu and Mo isotope variability is more subtle and close to analytical precision. Although the present situation is adequate for proceeding with GEOTRACES, it should be possible to improve the within-lab and between-lab precisions for some of these properties

Physical and Biogeochemical Controls on the Distribution of Dissolved Cadmium and its Isotopes in the Southwest Pacific Ocean

Cadmium stable isotope ratios (δ114Cd) have become a useful tool for oceanographers investigating the biogeochemical and physical processes that affect the nutrient-like distribution of the bioactive trace metal cadmium (Cd) throughout the oceans. Here, we present a meridional transect of dissolved Cd and δ114Cd from Japanese GEOTRACES section GP19 along 170°W from 64°S in the Southern Ocean to the equatorial Pacific. Along the GP19 section, the deep ocean (\u3e1500 m) shows small variability in dissolved Cd (0.75–0.9 nmol kg−1) and a homogeneous δ114Cd signature (+0.26 ± 0.06‰, 2SD, n = 60; relative to NIST SRM-3108). Adding these data to previously published work allows us to calculate a deep Pacific and Southern Ocean (\u3e1500 m) mean δ114Cd of +0.26 ± 0.10‰ (2SD, n = 436). Higher in the water column, depth profiles of Cd along the GP19 section exhibit a strong vertical gradient from a maximum (up to 0.9 nmol kg−1) at 1500–2000 m up to depleted surface waters (\u3c0.001 nmol kg−1 in the equatorial Pacific). This gradient in dissolved Cd concentration is associated with changes in dissolved δ114Cd, with values higher (+0.4 to +0.6‰) than the deep ocean average at intermediate depths (300–1500 m), and then a further increase towards high δ114Cd values (up to +0.9‰) in the surface ocean. Both patterns could be explained by one-dimensional biological cycling including preferential uptake of isotopically light Cd by phytoplankton, and such processes likely explain the surface patterns. At intermediate depths, however, the observed strong vertical Cd concentration and isotopic gradients instead result from the lateral isopycnal transport of Antarctic Intermediate Water (AAIW) and Subantarctic Mode Water (SAMW), both of which carry distinctly lower pre-formed Cd concentrations and higher δ114Cd values. These pre-formed signatures, which are imparted during water-mass formation in the Southern Ocean, are clearly conserved into the lower latitude Pacific as these water masses travel northward. Overall, the distribution of Cd and δ114Cd along the GP19 section is remarkably well explained by large scale mixing of water mass endmembers with defined δ114Cd signatures, emphasizing the importance of surface Southern Ocean processes for the distribution of trace metals such as Cd in the subsurface Southwest Pacific. At the regional scale, however, two other processes may overprint this mixing relationship. First, by comparison with the nearby Southeast Pacific GP16 section, we find that the δ114Cd signature of equatorial intermediate water masses shows little zonal variation across the equatorial Pacific, despite becoming enriched in dissolved Cd due to remineralization. We propose that this uniformity is explained by complete utilization of Cd in the surface tropical Pacific and remineralization of Cd with an isotopic signature similar to intermediate waters, therefore conserving the southern-sourced isotopic signature. Similarly, the observed increase of about 30% in deep ocean Cd concentrations from the South to the North Pacific is associated with a near-constant δ114Cd signal. These observations enable us to constrain the net δ114Cd of Cd added by remineralization to the deep ocean, with the caveat that such a signal is integrated over the entire Pacific, and that remineralization under different oceanic regimes such as HNLC areas may add Cd with different isotopic compositions to deep waters. Second, at GP19 stations close to the equator, subtle Cd depletion (relative to phosphate) is observed associated with low-oxygen subsurface waters, consistent with other studies from the North Pacific. Discerning the effects of such processes on Cd isotopic distributions is an important step to a more detailed understanding of the biogeochemical cycling of Cd in the modern ocean, and the application of δ114Cd as a tracer of past deep water circulation. This article is part of a special issue entitled: “Cycles of trace elements and isotopes in the ocean – GEOTRACES and beyond” - edited by Tim M. Conway, Tristan Horner, Yves Plancherel, and Aridane G. González