scholarly journals Exploring the role of environmental and ecological parameters on lithium isotope composition of marine carbonates

2021 ◽  
Author(s):  
Dongyu Chen ◽  
Lucas Weppe ◽  
Fanny Thibon ◽  
Axel Felbacq ◽  
Nathalie Vigier
2009 ◽  
Vol 146 (5) ◽  
pp. 674-689 ◽  
Author(s):  
K. MAŁKOWSKI ◽  
G. RACKI ◽  
D. DRYGANT ◽  
H. SZANIAWSKI

AbstractThe carbon and oxygen isotope composition of marine carbonates (δ13C and δ18O, respectively) are studied in the fossiliferous, stratigraphically well-constrained and remarkably expanded successions of Podolia, SW Ukraine, spanning the Silurian–Devonian transition. Significant isotopic shifts are directly comparable to previously published global secular trends in well-preserved brachiopod calcite isotopic ratios from this region, and therefore may be taken as a reliable primary record of seawater δ13C changes. The sections reveal a major positive δ13C excursion, with an amplitude above 6 ‰, beginning in the upper Pridoli and reaching peak values as heavy as +4.2 ‰ in the lowermost Lochkovian. This turnover in carbon cycling is followed by a general trend toward more negative δ13C values in the upper Lochkovian. The Podolian isotopic signals provide strong support for the previously inferred global biogeochemical perturbation across the Silurian–Devonian transition, reflecting a complex combination of palaeogeographical, biogeochemical and evolutionary processes in the late Caledonian geodynamic setting, with a likely undervalued role of the expanding vegetation in vast near-coastal shallows and deltas.


2014 ◽  
Vol 4 (1) ◽  
Author(s):  
Yan-Jie Tang ◽  
Hong-Fu Zhang ◽  
Etienne Deloule ◽  
Ben-Xun Su ◽  
Ji-Feng Ying ◽  
...  

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.


2021 ◽  
Author(s):  
Simon V. Hohl

<p>Cadmium (Cd) and isotope systematics are emerging tools for studying the biogeochemical cycling of micronutrients in the oceans, and sedimentary archives, as Cd concentrations in seawater show a nutrient-like behaviour, with surface depletion and deep water enrichments. However, the underlying processes are yet to be fully understood. The Cd concentration and isotopic composition of seawater are set by the balance of Cd inputs (and their isotopic composition) and the fractionation on removal to sedimentary sinks. The most favoured explanation is the Cd utilisation by marine phototrophic biomass, causing the surface water’s dissolved Cd pool depletion creating a depth gradient of increasing Cd concentrations and lighter isotopic compositions. Under incomplete oxidative recycling, organic matter may act as an effective Cd sink and authigenic minerals may store the ambient seawater’s Cd isotope composition.</p><p>Consequently, stable Cd isotope compositions in marine carbonates show broad variations linked to paleo-productivity and redox state changes. Additional fractionation processes govern the Cd isotopic compositions of marine sediments. Besides biological utilisation, experimental Cd partitioning into authigenic calcites or sulphides under variable redox and salinity conditions has been shown.  Therefore, when applying Cd isotopes in carbonates, other geochemical proxies must be evaluated very carefully to understand the involved Cd fractionation processes. This presentation aims to present the status quo of research done on authigenic and biologic carbonates and carbonate leachates in carbonatic shales to show the strengths and pitfalls of this new emerging bio-geoscience isotope proxy and its use for paleoenvironmental reconstructions on Earth and beyond.</p><p> </p><p> </p>


2019 ◽  
Vol 15 (2) ◽  
pp. 635-646 ◽  
Author(s):  
Holly L. Taylor ◽  
Isaac J. Kell Duivestein ◽  
Juraj Farkas ◽  
Martin Dietzel ◽  
Anthony Dosseto

Abstract. Lithium (Li) isotopes in marine carbonates have considerable potential as a proxy to constrain past changes in silicate weathering fluxes and improve our understanding of Earth's climate. To date the majority of Li isotope studies on marine carbonates have focussed on calcium carbonates. The determination of the Li isotope fractionation between dolomite and a dolomitizing fluid would allow us to extend investigations to deep times (i.e. Precambrian) when dolostones were the most abundant marine carbonate archives. Dolostones often contain a significant proportion of detrital silicate material, which dominates the Li budget; thus, pretreatment needs to be designed so that only the isotope composition of the carbonate-associated Li is measured. This study aims to serve two main goals: (1) to determine the Li isotope fractionation between Ca–Mg carbonates and solution, and (2) to develop a method for leaching the carbonate-associated Li out of dolostone while not affecting the Li contained within the detrital portion of the rock. We synthesized Ca–Mg carbonates at high temperatures (150 to 220 ∘C) and measured the Li isotope composition (δ7Li) of the precipitated solids and their respective reactive solutions. The relationship of the Li isotope fractionation factor with temperature was obtained: 103ln⁡αprec-sol=-(2.56±0.27)106(1)/T2+(5.8±1.3) Competitive nucleation and growth between dolomite and magnesite were observed during the experiments; however, there was no notable effect of their relative proportion on the apparent Li isotope fractionation. We found that Li isotope fractionation between the precipitated solid and solution is higher for Ca–Mg carbonates than for Ca carbonates. If the temperature of a precipitating solution is known or can be estimated independently, the above equation could be used in conjunction with the Li isotope composition of dolostones to derive the composition of the solution and hence make inferences about the past Li cycle. In addition, we also conducted leaching experiments on a Neoproterozoic dolostone and a Holocene coral. Results show that leaching with 0.05 M hydrochloric acid (HCl) or 0.5 % acetic acid (HAc) at room temperature for 60 min releases Li from the carbonate fraction without a significant contribution of Li from the siliciclastic detrital component. These experimental and analytical developments provide a basis for the use of Li isotopes in dolostones as a palaeo-environmental proxy, which will contribute to further advance our understanding of the evolution of Earth's surface environments.


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

2020 ◽  
Vol 117 (52) ◽  
pp. 33005-33010
Author(s):  
Meng Xing ◽  
Weiguo Liu ◽  
Xia Li ◽  
Weijian Zhou ◽  
Qiyuan Wang ◽  
...  

Anthropogenic combustion-derived water (CDW) may accumulate in an airshed due to stagnant air, which may further enhance the formation of secondary aerosols and worsen air quality. Here we collected three-winter-season, hourly resolution, water-vapor stable H and O isotope compositions together with atmospheric physical and chemical data from the city of Xi’an, located in the Guanzhong Basin (GZB) in northwestern China, to elucidate the role of CDW in particulate pollution. Based on our experimentally determined water vapor isotope composition of the CDW for individual and weighted fuels in the basin, we found that CDW constitutes 6.2% of the atmospheric moisture on average and its fraction is positively correlated with [PM2.5] (concentration of particulate matter with an aerodynamic diameter less than 2.5 μm) as well as relative humidity during the periods of rising [PM2.5]. Our modeling results showed that CDW added additional average 4.6 μg m−3 PM2.5 during severely polluted conditions in the GZB, which corresponded to an average 5.1% of local anthropogenic [PM2.5] (average at ∼91.0 μg m−3). Our result is consistent with the proposed positive feedback between the relative humidity and a moisture sensitive air-pollution condition, alerting to the nontrivial role of CDW when considering change of energy structure such as a massive coal-to-gas switch in household heating in winter.


2007 ◽  
Vol 260 (3-4) ◽  
pp. 582-596 ◽  
Author(s):  
Hans-Michael Seitz ◽  
Gerhard P. Brey ◽  
Jutta Zipfel ◽  
Ulrich Ott ◽  
Stefan Weyer ◽  
...  

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