Burial rates of organic matter along the eastern Canadian margin and stable isotope constraints on its origin and diagenetic evolution

1999 ◽  
Vol 160 (3-4) ◽  
pp. 251-270 ◽  
Author(s):  
Alfred N.N Muzuka ◽  
Claude Hillaire-Marcel
1989 ◽  
Vol 26 (4) ◽  
pp. 791-806 ◽  
Author(s):  
Martine Savard ◽  
Pierre-André Bourque

Carbonate units of two facie of the platformal upper reef complex of the Late Silurian West Point Formation, Gaspé Peninsula, Quebec, were studied to decipher their diagenetic evolution. The two facies were a reef-margin facies and a back-reef to lagoonal facies. Under the light microscope, only three broad cement phases were recognized. In contrast, cathodoluminescence observation revealed seven distinct generations of cements and a plethora of additional diagenetic features such as fracturing, internal brecciation, sulfatization, and stylolitization. The first four generations of cement were early marine and confined to the reef-margin facies. The subsequent three cement generations evolved in shallow to deeper burial environments and affected the reef-margin facies and the back-reef to lagoonal facies. C and O stable-isotope data support these deductions. Fracturing, internal brecciation, stylolitization, sulfatization, and the generation of the latest cements occurred during compaction and postcompaction stages. Lithification of the facies was rapid, with the pores completely occluded before a maximum burial depth of about 1 km was attained (based on conodont colour-alteration indices, organic-matter maturation data, and overall post-Silurian paleogeography).


2018 ◽  
Vol 63 (11) ◽  
pp. 1365-1380 ◽  
Author(s):  
Frank O. Masese ◽  
Kátya G. Abrantes ◽  
Gretchen M. Gettel ◽  
Kenneth Irvine ◽  
Steven Bouillon ◽  
...  

2017 ◽  
Vol 410 (3) ◽  
pp. 923-931 ◽  
Author(s):  
Alexandra C. Wiesheu ◽  
Ramona Brejcha ◽  
Carsten W. Mueller ◽  
Ingrid Kögel-Knabner ◽  
Martin Elsner ◽  
...  

2019 ◽  
Vol 124 (1) ◽  
pp. 149-174 ◽  
Author(s):  
Eliza J. Mathia ◽  
Thomas F. T. Rexer ◽  
K. Mark Thomas ◽  
Leon Bowen ◽  
Andrew C. Aplin

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):  
Pia Müller ◽  
Ulrich Heimhofer ◽  
Christian Ostertag-Henning

<p>The Oceanic Anoxic Event (OAE) 2 spanning the Cenomanian-Turonian boundary (93.5 Ma)<br>represents a major perturbation of the global carbon cycle and is marked by organic-rich<br>sediments deposited under oxygen-depleted conditions. In many studies the eruption of the<br>Caribbean LIP is considered to be the cause for rapidly increasing CO2 concentrations and<br>resulting global warming accompanied by widespread oceanic anoxia. In the Lower Saxony<br>Basin of northern Germany, the deposits of the OAE 2 are exposed in several industry drill<br>cores. In this study, the lower part of the OAE 2 has been studied in the HOLCIM 2011-3 drill<br>core. Sedimentary rocks are composed of limestones, marly limestones, marls and black<br>shales and have been analysed with a high-resolution stable isotope approach<br>(approximately one sample every 2 cm) combined with geochemical modelling. Using stable<br>carbon isotopes, bulk rock parameters and petrographic analysis, the onset of OAE 2 has<br>been investigated in detail. The high-resolution δ<sup>13</sup>C curve exhibits overall stable values<br>around 3 ‰ before the onset of the Plenus event. This background level is interrupted by<br>three short-lived and small but significant negative carbon isotope excursions (CIEs) down to<br>δ<sup>13</sup>C values of 2.5 ‰, 2.7 ‰ and 1.9 ‰. Immediately before the main rise in the Plenus bed,<br>a longer-lasting negative CIE down to 2.8 ‰ is observed, preceding the large positive CIE of<br>the OAE 2 to values of 5.2 ‰ over 33 ka. Thereafter, the δ<sup>13</sup>C values decrease to 3.5 ‰ over<br>a period of approximately 130 ka. The results can be correlated with the lower-resolution<br>data set of Voigt et al. (2008) but enable a more accurate characterization of the subtle<br>features of the CIE and hence events before and during this time interval. Carbon cycle<br>modelling with the modelling software SIMILE using a model based on Kump & Arthur (1999)<br>reveals that the negative excursion before the Plenus bed can be explained by a massive<br>volcanic pulse releasing of 0.95*10<sup>18</sup> mol CO2 within 14 ka. This amount corresponds to only<br>81 % of the calculated volume of CO<sub>2</sub> release during emplacement of the Caribbean LIP by<br>Joo et al. (2020). In the model the volcanic exhalation increases atmospheric CO<sub>2</sub><br>concentrations. This will increase global temperatures, intensify the hydrological cycle and<br>thus increase nutrient input into the ocean, resulting in an expansion of the oxygen minimum<br>zone, the development of anoxic conditions and an increase in the preservation potential for<br>organic material. In the model enhanced primary productivity and organic matter preservation<br>can be controlled by the implemented riverine phosphate input and the preservation factor for<br>organic matter. For the positive anomaly, the riverine phosphate input must be nearly<br>doubled (from 0.01 μmol/kg PO<sub>4 </sub>to 0.019 μmol/kg) for the period of the increasing δ<sup>13</sup>C<br>values (app. 33 ka), with a concomitant rise of the preservation factor from 1 % to 2 %. This<br>model scenario accurately reproduces the major features of the new high-resolution δ<sup>13</sup>C<br>record over the onset of the OAE 2 CIE.</p>


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