Tracer versus trace element diffusion: Diffusional decoupling of Sr concentration from Sr isotope composition

1989 ◽  
Vol 53 (11) ◽  
pp. 3015-3023 ◽  
Author(s):  
Don R Baker
2021 ◽  
Author(s):  
Sonja Lojen ◽  
Qasim Jamil ◽  
Tea Zuliani ◽  
Leja Rovan ◽  
Tjaša Kanduč ◽  
...  

<p>Precipitation of calcite from water fractionates strontium (Sr) isotopes because of preferential incorporation of light (<sup>86</sup>Sr) isotopes into the solid phase, making continental carbonates one of the most <sup>88</sup>Sr depleted reservoirs. It was suggested that carbonate precipitation is the most likely process controlling <em>δ</em><sup>88/86</sup>Sr composition of karst water. Therefore, the <sup>88</sup>Sr enrichment of river water could be used for the estimation of Sr and carbonate precipitation at catchment scale.</p><p>In the present study, we report on trace element partitioning and Sr isotope fractionation between tufa and water in the groundwater fed karst river Krka (Croatia). Water and tufa along with samples of bedrock and soil as the main contributors of dissolved and particulate Sr at seven main waterfalls and cascades along a 33 km section of the river were analysed for trace element and Sr isotope composition (<em>δ</em><sup>88/86</sup>Sr).</p><p>The highest δ<sup>88/86</sup>Sr values were measured in soils and in siliciclastic rocks, while in limestone, the <em>δ</em><sup>88/86</sup>Sr values were similar to those of old tufa precipitated in the period between 96 and 141 ky BP. Recent tufa, however, was considerably depleted in <sup>88</sup>Sr. The isotope fractionation between water and recent tufa varied a lot and was inversely correlated with Mg and Sr partitioning coefficients, while correlations with precipitation rates and temperature were rather weak. The <em>δ</em><sup>88/86</sup>Sr of recent tufa was strongly correlated with the stable isotope composition of organic carbon, which indicates that apart from hydrochemical, hydraulic parameters and temperature, plants and microbial communities that knowingly stimulate the tufa formation also affect the isotope fractionation of Sr.</p>


2006 ◽  
Vol 152 (5) ◽  
pp. 571-589 ◽  
Author(s):  
Friedrich Lucassen ◽  
Wolfgang Kramer ◽  
Viola Bartsch ◽  
Hans-Gerhard Wilke ◽  
Gerhard Franz ◽  
...  

2021 ◽  
Vol 62 (4) ◽  
pp. 415-426
Author(s):  
E.I. Lastochkin ◽  
G.S. Ripp ◽  
D.S. Tsydenova ◽  
V.F. Posokhov ◽  
A.E. Murzintseva

Abstract —We consider the isotope-geochemical features of epithermal fluorite deposits in Transbaikalia, including the REE compositions, Sr isotope ratios, Sm–Nd systems, and isotope compositions of oxygen, carbon, hydrogen, and sulfur. The 87Sr/86Sr ratios in fluorites are within 0.706–0.708, and the εNd values are negative. Oxygen in quartz, the main mineral of the deposits, has a light isotope composition (δ18O = –3.4 to +2.6‰), and the calculated isotope composition of oxygen in the fluid in equilibrium with quartz (δ18O = –9 to –16‰) indicates the presence of meteoric water. The latter is confirmed by analysis of the isotope compositions of oxygen and hydrogen in gas–liquid inclusions in fluorites from three deposits. These isotope compositions are due to recycling caused by the impact of shallow basic plutons. The isotope composition of sulfur indicates its deep source. During ascent, sulfur became enriched in its light isotope (δ34S = –1.8 to –7.7‰). We assess the association of fluorite ores with basaltoids widespread in the study area. The isotope and geochemical parameters suggest their spatial proximity. Probably, the basaltoids were responsible for the recycling of meteoric water. It is shown that the epithermal fluorite deposits formed by the same mechanism as fissure–vein thermal waters in western Transbaikalia.


2019 ◽  
Vol 10 (2) ◽  
pp. 289-308 ◽  
Author(s):  
T. A. Osipova ◽  
G. A. Kallistov ◽  
M. V. Zaitseva

The article is focused on the morphology, trace element composition, U‐Pb and Lu‐Hf systems in zircon in high‐Mg diorite of the Chelyabinsk granitoid massif. Our analytical studies of the U‐Pb and Lu‐Hf isotope systems and the trace element composition were performed using mass spectrometry (MS) with inductively coupled plasma (ICP) and laser ablation (LA) of samples. It is established that the zircon formed at the last stages of crystallization of the basic melt under subsolidus conditions at low (600–700 °C) temperatures, which distinguishes it from the zircon of most other high‐Mg rocks of the intermediate composition. The internal structure of the zircon and the concentration of trace elements are locally altered under the influence of a fluid, which led to a partial disruption of the U‐Pb and Lu‐Hf isotopic systems. For the least altered areas in the zircon crystals, the age of crystallization of the parent high‐Mg melt is 362±2 Ma, which coincides with the age estimated from the geological data. Considering the isotope composition of Hf in the zircon and the trace element concentrations, there are grounds to relate the formation of high‐Mg diorite in the Chelyabinsk granitoid massif with a mixed mantle‐crustal source.


2020 ◽  
Vol 17 (23) ◽  
pp. 5989-6015
Author(s):  
Quentin Charbonnier ◽  
Julien Bouchez ◽  
Jérôme Gaillardet ◽  
Éric Gayer

Abstract. The biological cycle of rock-derived nutrients on the continents is a major component of element transfer between the Earth's surface compartments, but its magnitude currently remains elusive. The use of the stable isotope composition of rock-derived nutrients, which can be fractionated during biological uptake, provides a promising path forward with respect to quantifying biological cycling and its overall contribution to global element cycling. In this paper, we rely on the nutrient-like behaviour of the trace element barium (Ba) and use its elemental and stable isotope compositions in dissolved and sediment load river samples to investigate biological cycling in the Amazon Basin. From these measurements, we show that dissolved Ba mainly derives from silicate rocks, and a correlation between dissolved Ba and K abundances suggests that biological cycling plays a role in the Ba river budget. Furthermore, the isotope composition of Ba (δ138Ba) in the dissolved load was found to be significantly different from that of the parent silicate rocks, implying that dissolved Ba isotopic signatures are affected by (i) the precipitation of soil-forming secondary phases as well as (ii) biological uptake and release from dead organic matter. Results from an isotope mass balance method applied to the river dissolved load data indicate that, after its release to solution by rock weathering, Ba is partitioned between the river dissolved load, secondary weathering products (such as those found in soils and river sediments), and the biota. In most sub-catchments of the Amazon, river Ba abundances and isotope compositions are significantly affected by biological cycling. Relationships between estimates of Ba cycled through biota and independent metrics of ecosystem dynamics (such as gross primary production and terrestrial ecosystem respiration) allow us to discuss the role of environmental parameters such as climate or erosion rates on the biological cycling of Ba and, by extension, the role of major rock-derived nutrients. In addition, catchment-scale mass and isotope budgets of Ba show that the measured riverine export of Ba is lower than the estimated delivery of Ba to the Earth surface through rock alteration. This indicates the existence of a missing Ba component, which we attribute to the formation of Ba-bearing particulate organics (possibly accumulating as soil organic matter or currently growing biomass within the catchments) and to organic-bound Ba exported as “unsampled” river particulate organic matter. Given our findings on the trace element Ba, we explore whether the river fluxes of most major rock-derived nutrients (K, Mg, Ca) might also be significantly affected by biological uptake or release. A first-order correction of river-derived silicate weathering fluxes from biological cycling shows that the carbon dioxide (CO2) consumption by silicate weathering at the mouth of the Amazon could be several times higher than the previously reported value of 13 × 109 mol CO2 yr−1 (Gaillardet et al., 1997). Overall, our study clearly shows that the chemical and isotope compositions of rivers in the Amazon – and most likely in other large river basins – bear a biological imprint, thereby challenging common assumptions made in weathering studies.


2008 ◽  
Vol 23 (4) ◽  
pp. 321-330 ◽  
Author(s):  
Tim S. Brewer ◽  
Melanie J. Leng ◽  
Anson W. Mackay ◽  
Angela L. Lamb ◽  
Jonathan J. Tyler ◽  
...  

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