Early And Middle Cambrian Carbon And Strontium Isotopic Chemostratigraphy And The Influence Of Bioturbation On The Carbon Cycle PDF Download

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The Phanerozoic Carbon Cycle

The Phanerozoic Carbon Cycle
Author: Robert A. Berner
Publisher: Oxford University Press
Total Pages: 158
Release: 2004-08-19
Genre: Science
ISBN: 0190291613

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The term "carbon cycle" is normally thought to mean those processes that govern the present-day transfer of carbon between life, the atmosphere, and the oceans. This book describes another carbon cycle, one which operates over millions of years and involves the transfer of carbon between rocks and the combination of life, the atmosphere, and the oceans. The weathering of silicate and carbonate rocks and ancient sedimentary organic matter (including recent, large-scale human-induced burning of fossil fuels), the burial of organic matter and carbonate minerals in sediments, and volcanic degassing of carbon dioxide contribute to this cycle. In The Phanerozoic Carbon Cycle, Robert Berner shows how carbon cycle models can be used to calculate levels of atmospheric CO[2 and O[2 over Phanerozoic time, the past 550 million years, and how results compare with independent methods. His analysis has implications for such disparate subjects as the evolution of land plants, the presence of giant ancient insects, the role of tectonics in paleoclimate, and the current debate over global warming and greenhouse gases


Carbon, Sulfur, and Strontium Isotope Stratigraphy of the Lower-Middle Ordovician, Great Basin, USA

Carbon, Sulfur, and Strontium Isotope Stratigraphy of the Lower-Middle Ordovician, Great Basin, USA
Author: Cole T. Edwards
Publisher:
Total Pages:
Release: 2014
Genre:
ISBN:

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Long-term d13C and d34S trends indicate two pulses of oxygenation occurred during periods of increased burial rates of organic matter and pyrite. These oxygenation pulses are roughly coincident with the first major biodiversification pulses during the Middle Ordovician and suggest that increasing oxygen levels played an important role in global biodiversity. Continued research focused on resolving the precise timing of biodiversification globally or within individual basins will be able use chemostratigraphic correlation to compare with the d13C, d34S, or 87Sr/86Sr and isotopic data presented here.


ASA News

ASA News
Author:
Publisher:
Total Pages: 572
Release: 2003
Genre: Africa
ISBN:

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The Carbon Cycle Perturbation Associated with the End-triassic Mass Extinction

The Carbon Cycle Perturbation Associated with the End-triassic Mass Extinction
Author: Aviv Bachan Dovrat
Publisher:
Total Pages:
Release: 2013
Genre:
ISBN:

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The end-Triassic mass extinction is recognized as one of the five most severe biotic crises of the Phanerozoic. It was accompanied by an equally profound geochemical perturbation. A negative carbon isotope excursion and carbonate poor boundary-marl occur coincident with the disappearance of the Triassic biota at many sites around the globe. These are followed by a protracted positive carbon isotope excursion extending for hundreds of meters above the Triassic-Jurassic boundary. The main hypothesized driver for the carbon cycle perturbation is the release of volatiles associated with the emplacement of the Central Atlantic Magmatic Province (CAMP). However, the exact cause-and-effect relationships between the physical drivers and the geochemical responses have remained elusive. In this thesis I expand our knowledge of the end-Triassic carbon cycle perturbation by adding a large body of new carbon and oxygen stable isotope data, both in the immediate vicinity of the Triassic-Jurassic boundary and in the hundreds of meters following it. This data includes the first published extended carbon isotope curve containing measurements of both organic and carbonate carbon from the same samples. I also develop a flexible multi-element numerical box model based on a novel interpretation of the link that alkalinity provides between ocean chemistry and the cycling of elements on geologic timescales. I then utilize the model to make predictions regarding the impacts of the hypothesized carbon release on the chemistry of the ocean-atmosphere system and the resulting geochemical trends. Specifically, in Chapter 1 I present close to 1000 new data points from both organic and carbonate carbon, and detailed descriptions of the localities and geological settings in which they occur. I show that the previously observed protracted positive carbon isotope excursion that occurs above the Triassic-Jurassic boundary in many places, can be traced for tens of kilometers across sections in the southern Alps, and occurs in a correlative position hundreds of kilometers away in the southern Apennines. The spatial extent of the perturbation, and its occurrence in both organic and carbonate phases suggests that it is unlikely to be of diagenetic origin. Additionally, its stratigraphic extent suggests that the carbon cycle perturbation that began at the boundary persisted for a substantial period of geologic time (likely hundreds of thousands to millions of years) following the extinction event. In Chapter 2 I develop and apply a numerical carbon cycle model to investigate the underlying mechanism for the isotopic trends described in Chapter 1. I show that considering the role of alkalinity in the ocean leads to the conclusion that an increase in the burial of organic carbon that is unaccompanied by an increase in the input of carbon, can only lead to a reduction in the partial pressure of carbon dioxide in the atmosphere. To produce a positive excursion that is accompanied by an increase in atmospheric carbon dioxide levels, the amount of carbon brought into the exogenic carbon pool must be increased. The results of this modeling exercise elucidate the mechanism that underlies the common association between volcanic degassing and positive carbon isotope excursions in the geologic record. In Chapter 3 I focus on the Triassic-Jurassic boundary interval, and examine the relationship between the carbonate-poor interval associated with the extinction and the negative carbon isotope excursion that occurs within it. I show that the negative excursion is unique to the boundary marl, and does not occur in other stratigraphically adjacent carbonate-poor beds, arguing against a strict association between the carbon isotope value and percent carbonate. Rather, it is likely that a third factor was responsible for simultaneously driving both trends. First, I examine the possibility of anaerobic respiration of organic carbon within the marl having driven the precipitation of carbonate depleted in carbon-13 and oxygen-18. Second, I investigate the hypothesis that a rapid release of isotopically depleted carbon concomitantly reduced the carbon isotope composition and carbonate saturation state of the ocean. I conclude that if the negative excursion represents the release of depleted volatiles, the duration of the release and the associated acidification event must have been extremely short, on the order of a few thousand years, and that the isotopic composition of the released volatiles must have been far below mantle values. Together these three chapters consist of a coherent and thorough examination of the carbon isotopic record of the end-Triassic mass extinction, and represent a strong step forward in our understanding of the physical events and resulting geochemical cascades that led to the biotic crisis.


Carbon and Sulfur Cycling in Early Paleozoic Oceans

Carbon and Sulfur Cycling in Early Paleozoic Oceans
Author: Cara Kim Thompson
Publisher:
Total Pages: 218
Release: 2011
Genre:
ISBN:

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Here, I evaluate biospheric evolution during the Ordovician using high-resolution inorganic carbon and sulfur (carbonate-associated sulfate and pyrite) isotope profiles for Early Ordovician to early Late Ordovician strata from geographically distant sections in Western Newfoundland and the Argentine Precordillera. Additionally, I present new, high-resolution U-Pb ages for volcanic ash beds within strata of the Argentine Precordillera. Carbon isotope data record subdued variation that is typical of Early to Middle Ordovician strata worldwide. By contrast, sulfur isotopic compositions of carbonate-associated sulfate reveal a complex signal of short-term, rhythmic variation superimposed over a longer-term signal. This short-term, rhythmic variation occurs in all sections and appears to be unrelated to lithology or depositional environment, suggesting preservation of an oceanographic signal. I interpret this signal to reflect a combination of a marine sulfate reservoir that was likely much smaller than the modern, the persistence of a substantial deep-ocean hydrogen sulfide reservoir, and the episodic oxidation of a portion of the deep-ocean euxinic reservoir. Persistent euxinia likely resulted from decreased solubility of oxygen in warmer water and/or sluggish oceanic circulation during greenhouse conditions that reduced vertical ventilation. A dramatic change in the behavior of carbonate-associated sulfate and pyrite in the Middle Ordovician is interpreted to reflect a major oceanographic event that records the initial transition from Ordovician greenhouse to icehouse states. I suggest that the initiation of downwelling of increasingly cool, oxygen-rich surface water resulted in widespread oxidation of much of the deep ocean hydrogen sulfide reservoir and concomitant limitation of marine pyrite formation. It is unknown, however, why sea surface temperatures declined through the Early to Middle Ordovician. Explosive volcanism does not appear to be a primary climate driver, based on the timing of Argentinian K-bentonite formations relative to marine records of sea surface temperature, carbon and strontium isotopic composition. Rather, long-term positive feedback between organic carbon burial rates and productivity may have increased carbon dioxide drawdown, ultimately driving a gradual decrease in sea surface temperatures in the Early to Middle Ordovician.