scholarly journals Dispersed Carbon in Basalts of the Altered Oceanic Crust: Isotope Composition and Mechanisms of Formation

Petrology ◽  
2021 ◽  
Vol 29 (6) ◽  
pp. 614-626
Author(s):  
V. B. Polyakov ◽  
S. N. Shilobreeva
Keyword(s):  
Isotopic Composition ◽  
Oceanic Crust ◽  
Elemental Carbon ◽  
Dissolved Inorganic Carbon ◽  
Isotope Composition ◽  
Adsorbed Layer ◽  
Total Carbon ◽  
Boudouard Reaction ◽  
Carbonate Phase ◽  
Basalt Glasses

Abstract Carbon contents and isotopic compositions were compared in the basalt groundmass of the oceanic crust of different age in the zone of the East Pacific Rise. In samples the basalt groundmass of the ancient oceanic crust (~270 Ma, ODP Site 801C) in which a carbonate phase was found, the isotopic composition of the oxidized carbon (δ13C = ±1.5‰) indicates that this carbon was formed by the precipitation of seawater dissolved inorganic carbon (DIC). In the samples in which no carbonate phase was identified, the low concentration (<0.1 wt % CO2) of oxidized dispersed carbon and its isotopic composition (δ13C < –7‰) are in the range of values typical of carbon dissolved in basalt glasses without crystallinity. This makes it possible to relate the oxidized dispersed carbon to residual carbon dissolved in the magmatic melt after CO2 degassing. The precipitation of DIC results in a positive correlation between the concentration of total carbon and its δ13C values, along with the formation of a carbonate phase. The application of this criterion to basalt groundmass samples of the young crust (~15 Ma, ODP Site 1256D) showed that oxidized dispersed carbon in the young oceanic crust groundmass was not formed by the precipitation of DIC, contradicting the generally accepted paradigm. Constant concentration and δ13C values of the reduced dispersed carbon in the basalt groundmass of the young and ancient oceanic crusts, including lithological zones where microbial activity has not been recorded, indicate that the most probable model is high-temperature abiogenic generation of reduced dispersed carbon near the ridge axis. The Fischer–Tropsch synthesis and/or Bell–Boudouard reaction provide a possible basis for the abiogenic model. The Bell–Boudouard reaction 2CO = C + CO2 leads to the formation of an adsorbed layer of elemental carbon on the fresh surfaces of minerals during background alteration of the oceanic basalt crust. The CO2–CO gas-phase equilibrium maintains the necessary depletion of the newly formed elemental carbon in the 13C isotope to δ13C < –20‰. Abiogenic models for the origin of the isotopically light reduced dispersed carbon in the basalt groundmass do not assume the presence of carbon depleted in the heavy 13C isotope in the magmatic melt.

scholarly journals Variations of Isotopic Composition of Carbon in the Karst Environment from Southern Poland, Present and Past

Radiocarbon ◽  
1999 ◽  
Vol 41 (1) ◽  
pp. 81-97 ◽  
Author(s):  
Anna Pazdur ◽  
Tomasz Goslar ◽  
Mirosława Pawlyta ◽  
Helena Hercman ◽  
Michał Gradziński
Keyword(s):  
Isotopic Composition ◽  
Dissolved Inorganic Carbon ◽  
Isotope Composition ◽  
Mean Values ◽  
Calcium Carbonates ◽  
Suitable Material ◽  
Southern Poland ◽  
Karst Environment ◽  
Biogenic Carbon ◽  
Dating Methods

We describe a comprehensive study of carbon isotopes in several karst springs and their environs in a contemporary karst environment in the region of the Cracow-Wieluñ Upland and Western Tatra Mountains, Southern Poland. We collected samples of water, plants and carbonate deposited on aquatic plants, and obtained 13C values and 14C concentrations. We also investigated a group of the youngest calcium carbonates from caves where deposition is still being observed or ceased no more than a few hundred years ago. The determination of a 14C dilution factor (q) in these carbonates allows us to determine the “true” radiocarbon ages of old speleothems from caves in the area under investigation and enables the use of old speleothems as suitable material for extending the 14C calibration time scale, the “Absolute” age having been determined by U/Th or amino acid racemization (AAR) dating methods. Measurements of δ13C and 14C concentrations were made on dissolved inorganic carbon (DIC) extracted from water samples. Calculated values of q range from 0.55 to 0.68 and δ13C values range from −10% to −13% versus VPDB with mean values equal to 0.65 and −12%, respectively. Results indicate that the dissolution process of limestone bedrock is a closed system with the dominating contributor being biogenic carbon dioxide.Isotopic composition of carbon in contemporary plants collected at the karstic springs at 3 localities is highly diverse, with different species distinctly varying in both q and δ13C values. Extremely light values of 13C (under −40%), observed in Algae and Hyloconium splendens, are correlated with 14C concentrations that are much lower than 100 pMC. Small systematic changes of isotopic composition were found in plants of the same species collected along streams at various distances from the spring. The youngest calcium carbonates from different caves show a relatively high scatter of both δ13C values and 14C concentration. The lower reservoir effect for 14C is observed in samples with higher value of δ13C, indicating equilibrium conditions in the sedimentation of carbonate. Pazdur et al. (1995b) presented 14C dating results and paleoclimatic interpretation of 170 14C analyses of 89 speleothems from 41 caves obtained through 1994. Investigations continued until early 1997, during which time a speleothem, JWi2, was dated by 14C, U/Th and AAR dating methods, and its stable isotope composition (δ13C and δ18O) analyzed in detail (reported here). Carbon isotope analyses indicate very large differences among results obtained by U/Th, AAR, and 14C dating methods.

scholarly journals Multi-Technique groundwater flow system analysis and dating of deep aquifers in Alessandria Basin (Piedmont - IT)

2020 ◽  
Author(s):  
Nicola Quaranta ◽  
Elena Cogo ◽  
Adriano Simoni ◽  
Elisa Sacchi ◽  
Mariachiara Caschetto ◽  
...  
Keyword(s):  
Isotopic Composition ◽  
Groundwater Flow ◽  
System Analysis ◽  
Dissolved Inorganic Carbon ◽  
Flow System ◽  
Isotope Composition ◽  
Radioactive Isotopes ◽  
Deep Groundwater ◽  
Groundwater Flow System ◽  
Deep Aquifers

The aim of the study was to set up a protection system from pollution of the deep aquifer of the Alessandria basin, by redefining the recharge areas, focused on this portion of Piedmont territory, and therefore by creating some reserve areas of deep groundwater, to be preserved for future human drinking purposes. In addition to the classical hydrodynamic and geochemical monitoring techniques, the groundwaters were analyzed with reference to a monitoring network of 25 selected wells with deep screens (80-300 m below ground surface) combining radiochemical dating (14C and δ13C of dissolved inorganic carbon - DIC) with anthropogenic tracers (CFCs, SF6) as indicators of recent recharge/ mixing. Stable isotope composition (δ2H and δ18O – H2O) was assessed during a 1-year sampling of snow-rain precipitations gauges distributed in altitude in order to define Local Meteoric Water Lines; the isotopic composition was also seasonally measured for the main rivers and in selected deep-wells. The 3D numerical model was implemented in FEflow platform and calibrated on the basis of the available monitoring data; it was used as a support tool in the delimitation of the recharge areas, starting from the analysis of the distribution of flows. This model was crucial for delimiting the “reserve areas”, since it was able to simulate groundwater flows using both purely advective transport conditions (particle tracking technique), and more realistic conditions of advective and dispersive transport, by introducing dispersive parameters and using the Life Time Expectancy (LTE) reservoir distribution. The integrated use of “traditional” techniques of regional groundwater flow system monitoring (hydrochemistry, stable isotopic composition) and of dating techniques based on radioactive isotopes and anthropogenic tracers, provided a reliable support to the validation of flow and transport simulation model, oriented to identify recharge areas and “reserve areas” of future extraction of deep groundwater for drinking purpose.

Os isotopic composition of western Aleutian adakites: Implications for the Re/Os of oceanic crust processed through hot subduction zones

2021 ◽  
Vol 292 ◽  
pp. 452-467
Author(s):  
Rachel Bezard ◽  
Simon Turner ◽  
Bruce Schaefer ◽  
Gene Yogodzinski ◽  
Kaj Hoernle
Keyword(s):  
Isotopic Composition ◽  
Oceanic Crust ◽  
Subduction Zones

scholarly journals Ecosystem effects of CO<sub>2</sub> concentration: evidence from past climates

2009 ◽  
Vol 5 (2) ◽  
pp. 937-963 ◽  
Author(s):  
I. C. Prentice ◽  
S. P. Harrison
Keyword(s):  
Forest Cover ◽  
Dissolved Inorganic Carbon ◽  
Net Primary Production ◽  
Isotope Composition ◽  
Late Quaternary ◽  
Co2 Concentration ◽  
C3 Plants ◽  
Sea Level Changes ◽  
Co2 Effects ◽  
Concentration Changes

Abstract. Atmospheric CO2 concentration has varied from minima of 170–200 ppm in glacials to maxima of 280–300 ppm in the recent interglacials. Photosynthesis by C3 plants is highly sensitive to CO2 concentration variations in this range. Physiological consequences of the CO2 changes should therefore be discernible in palaeodata. Several lines of evidence support this expectation. Reduced terrestrial carbon storage during glacials, indicated by the shift in stable isotope composition of dissolved inorganic carbon in the ocean, cannot be explained by climate or sea-level changes. It is however consistent with predictions of current process-based models that propagate known physiological CO2 effects into net primary production at the ecosystem scale. Restricted forest cover during glacial periods, indicated by pollen assemblages dominated by non-arboreal taxa, cannot be reproduced accurately by palaeoclimate models unless CO2 effects on C3-C4 plant competition are also modelled. It follows that methods to reconstruct climate from palaeodata should account for CO2 concentration changes. When they do so, they yield results more consistent with palaeoclimate models. In conclusion, the palaeorecord of the Late Quaternary, interpreted with the help of climate and ecosystem models, provides evidence that CO2 effects at the ecosystem scale are neither trivial nor transient.

scholarly journals Seasonal variations in nitrate isotope composition of three rivers draining into the North Sea

2010 ◽  
Vol 7 (4) ◽  
pp. 6051-6088 ◽  
Author(s):  
A. Deek ◽  
K. Emeis ◽  
U. Struck
Keyword(s):  
Isotopic Composition ◽  
North Sea ◽  
Isotope Composition ◽  
Atmospheric Oxygen ◽  
Isotope Effects ◽  
Nitrate Sources ◽  
Particulate Nitrogen ◽  
Soil Nitrification ◽  
Mean Values ◽  
Δ 15N

Abstract. Nitrate loading of coastal ecosystems by rivers that drain industrialised catchments continues to be a problem in the South Eastern North Sea, in spite of significant mitigation efforts over the last 2 decades. To identify nitrate sources, sinks, and turnover in three German rivers that discharge into the German Bight, we determined δ 15N-NO3- and δ18O- NO3- in nitrate and δ 15N of particulate nitrogen for the period 2006–2009 (biweekly samples). The nitrate loads of Rhine, Weser and Ems varied seasonally in magnitude and δ 15N-NO3- (6.5–21‰), whereas the δ 18O-NO3- (-0.3–5.9‰) and δ 15N-PN (4–14‰) were less variable. Overall temporal patterns in nitrate mass fluxes and isotopic composition suggest that a combination of nitrate delivery from nitrification of soil ammonia in the catchment and assimilation of nitrate in the rivers control the isotopic composition of nitrate. Nitrification in soils as a source is indicated by low δ 18O-NO3- in winter, which traces the δ 18O of river water. Mean values of δ 18O-H2O were between –9.4‰ and –7.3‰; combined in a ratio of 2:1 with the atmospheric oxygen δ 18O of 23.5‰ agrees with the found δ 18O of nitrate in the rivers. Parallel variations of δ 15N-NO3- and δ 18O-NO3- within each individual river are caused by isotope effects associated with nitrate assimilation in the water column, the extent of which is determined by residence time in the river. Assimilation is furthermore to some extent mirrored both by the δ 15N of nitrate and particulate N. Although δ 15-NO3- observed in Rhine, Weser and Ems are reflected in high average δ 15N-PN (between 6‰ and 9‰, both are uncorrelated in the time series due to lateral and temporal mixing of PN. That a larger enrichment was consistently seen in δ 15N-NO3- relative to δ 18O-NO3- is attributed to constant additional diffuse nitrate inputs deriving from soil nitrification in the catchment area. A statistically significant inverse correlation exists between increasing δ 15N-NO3- values and decreasing NO3- concentrations. This inverse relationship – observed in each seasonal cycle – together with a robust relationship between human dominated land use and δ 15N-NO3- values demonstrates a strong influence of human activities and riverine nitrate consumption efficiency on the isotopic composition of riverine nitrate.

Status-quo of carbonate cadmium isotope compositions as a paleo-productivity proxy

2021 ◽  
Author(s):  
Simon V. Hohl
Keyword(s):  
Isotopic Composition ◽  
Isotope Composition ◽  
Status Quo ◽  
Ambient Seawater ◽  
Isotopic Compositions ◽  
Marine Carbonates ◽  
The Status ◽  
State Changes ◽  
Underlying Processes ◽  
Isotope Systematics

&lt;p&gt;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&amp;#8217;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&amp;#8217;s Cd isotope composition.&lt;/p&gt;&lt;p&gt;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. &amp;#160;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.&lt;/p&gt;&lt;p&gt;&amp;#160;&lt;/p&gt;&lt;p&gt;&amp;#160;&lt;/p&gt;

scholarly journals Evaluating Dissolved Inorganic Carbon Cycling in a Forested Lake Watershed Using Carbon Isotopes

Radiocarbon ◽  
1992 ◽  
Vol 34 (3) ◽  
pp. 636-645 ◽  
Author(s):  
Ramon Aravena ◽  
S. L. Schiff ◽  
S. E. Trumbore ◽  
P. J. Dillon ◽  
Richard Elgood
Keyword(s):  
Isotopic Composition ◽  
Carbon Isotopes ◽  
Inorganic Carbon ◽  
Dissolved Inorganic Carbon ◽  
Carbon Isotopic Composition ◽  
Isotopic Fractionation ◽  
Early Spring ◽  
Late Winter ◽  
Isotope Pattern ◽  
Carbon Isotopic

Dissolved inorganic carbon (DIC) is the main acid buffer in forested lake watersheds in Canada. We used carbon isotopes (13C, 14C) to evaluate the production and cycling of DIC in an acid-sensitive lake watershed of the Precambrian Shield. Soil CO2, groundwater and stream DIC were characterized chemically and isotopically. Soil CO2 concentration profiles reflect both changes in production and in losses due to diffusion. δ13C soil CO2 profiles (δ13C values of −23‰ in summer, slightly enriched during the fall and −25%‰ during the winter) are a reflection of the isotopic composition of the sources and changes in isotopic fractionation due to diffusion. Carbon isotopic composition (13C, 14C) of the groundwater and stream DIC clearly indicate that weathering of silicates by soil CO2 is the main source of DIC in these watersheds. 14C data show that, in addition to recent groundwater, an older groundwater component with depleted 14C activity is also present in the bedrock. The carbon isotope pattern in the groundwater also implies that, besides the main springtime recharge events, contributions to the groundwater may also occur during late winter/early spring.

Stable isotopes reveal post-release trophodynamic and ontogenetic changes in a released finfish, mulloway (Argyrosomus japonicus)

2010 ◽  
Vol 61 (3) ◽  
pp. 302 ◽  
Author(s):  
Matthew D. Taylor ◽  
Debashish Mazumder
Keyword(s):  
Stable Isotopes ◽  
Isotopic Composition ◽  
Turnover Rate ◽  
Isotope Composition ◽  
Wild Fish ◽  
Ontogenetic Changes ◽  
Nitrogen Stable Isotope ◽  
Δ13c And Δ15n ◽  
Carbon And Nitrogen ◽  
Nitrogen Isotopic Composition

Carbon and nitrogen stable isotope ratios were analysed for hatchery-reared, recaptured and wild mulloway, Argyrosomus japonicus, to investigate temporal and growth-related changes in isotopic composition for stocked fish after release, and to evaluate changes in isotopic composition in terms of ontogenetic dietary switches. δ13C and δ15N values decreased and increased, respectively, after release. The isotope composition of released fish was distinct from wild fish until 200 days after release, but after 200 days post-release fish did not differ significantly from wild fish of similar or greater sizes. Abrupt dietary transitions from crustaceans to teleost fish (>50 cm total length (TL)) were evident in a rapid δ13C and δ15N change in wild mulloway, and δ15N was significantly greater in wild fish >65 cm TL compared with wild fish <50 cm TL. Multivariate carbon and nitrogen isotopic data were suitable for separating stocked and wild fish for up to 200 days after release, but did not separate wild fish grouped according to dietary composition. Carbon and nitrogen isotopic composition closely reflected dietary transitions and rapid adaptation by stocked mulloway to wild diets, which was evident in a high tissue turnover rate of up to 0.017 day–1. Stable isotopes are a useful tool for examining the integration of released fish into stocked ecosystems and can be used to describe convergence in the diets of wild and released fish.

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