The Response of Marine Carbonate Chemistry to Rapid Carbon Injection During the Paleocene-eocene Thermal Maximum

The Response of Marine Carbonate Chemistry to Rapid Carbon Injection During the Paleocene-eocene Thermal Maximum

Author:

Publisher:

Published: 2015

Total Pages: 167

ISBN-13: 9781321676150

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This dissertation reconstructs the response of marine carbonate chemistry to rapid carbon injection during the Paleocene-Eocene Thermal Maximum (PETM). Chapter 1 uses boron-based proxies to reconstruct ocean acidification during the PETM for the first time, concluding that surface seawater pH declined by ∼0.3 units at the onset of the event, and remained acidified for at least 70 thousand years before recovering in step with temperature and the carbon isotopic signature of the PETM. Chapter 2 describes a new sedimentary record of the PETM from the deep North Atlantic which provides the first evidence for a hypothesized "overshoot" of carbonate saturation in the aftermath of the PETM in response to long-term weathering feedbacks on climate. Stable isotope records from that section demonstrate that this overshoot occurred during the recovery of the PETM, ∼70 thousand years after its onset, which provides novel constraints on the evolution of the carbonate compensation depth over the event. Finally, Chapter 3 uses these new (and previous) records to constrain carbon cycle model simulations of the PETM. Consistent runs require both a large initial release as well as a protracted release over tens of thousands of years (possibly representing a slow positive feedback to warming) and the removal of isotopically light carbon to accelerate the PETM recovery, likely representing organic carbon burial. No consistent scenarios feature under-saturated conditions in the surface ocean during the PETM, consistent with the lack of calcifier extinctions during the event. Comparison of the most consistent PETM scenarios with forecasts of anthropogenic carbon emissions demonstrate that carbonate chemistry change during the PETM was less severe and far more gradual than what might be expected in coming centuries.


Boron Proxies in Paleoceanography and Paleoclimatology

Boron Proxies in Paleoceanography and Paleoclimatology

Author: Bärbel Hönisch

Publisher: John Wiley & Sons

Published: 2019-05-13

Total Pages: 241

ISBN-13: 1119010632

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Anthropogenic carbon dioxide emissions do not only warm our planet but also acidify our oceans. It is currently unclear to which degree Earth’s climate and marine life will be impacted by these changes but information from Earth history, particularly the geochemical signals of past environmental changes stored in the fossil remains of marine organisms, can help us predict possible future changes. This book aims to be a primer for scientists who seek to apply boron proxies in marine carbonates to estimate past seawater carbonate chemistry and atmospheric pCO2. Boron proxies (δ11B and B/Ca) were introduced nearly three decades ago, with subsequent strides being made in understanding their mechanistic functioning. This text reviews current knowledge about the aqueous systematics, the inorganic and biological controls on boron isotope fractionation and incorporation into marine carbonates, as well as the analytical techniques for measurement of boron proxies. Laboratory and field calibrations of the boron proxies are summarized, and similarities between modern calibrations are explored to suggest estimates for proxy sensitivities in marine calcifiers that are now extinct. Example applications illustrate the potential for reconstructing paleo-atmospheric pCO2 from boron isotopes. Also explored are the sensitivity of paleo-ocean acidity and pCO2 reconstructions to boron isotope proxy systematics that are currently less well understood, including the elemental and boron isotopic composition of seawater through time, seawater alkalinity, temperature and salinity, and their collective impact on the uncertainty of paleo-reconstructions. The B/Ca proxy is based on the same mechanistic principles as the boron isotope proxy, but empirical calibrations suggest seawater pH is not the only controlling factor. B/Ca therefore has the potential to provide a second carbonate parameter that could be paired with δ11B to fully constrain the ocean carbonate system, but the associated uncertainties are large. This text reviews and examines what is currently known about the B/Ca proxy systematics. As more scientists embark on characterizing past ocean acidity and atmospheric pCO2, Boron in Paleoceanography and Paleoclimatology provides a resource to introduce geoscientists to the opportunities and complications of boron proxies, including potential avenues to further refine them.


Large Igneous Provinces

Large Igneous Provinces

Author: Richard E. Ernst

Publisher: John Wiley & Sons

Published: 2021-02-09

Total Pages: 532

ISBN-13: 1119507456

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This book is Open Access. A digital copy can be downloaded for free from Wiley Online Library. Exploring the links between Large Igneous Provinces and dramatic environmental impact An emerging consensus suggests that Large Igneous Provinces (LIPs) and Silicic LIPs (SLIPs) are a significant driver of dramatic global environmental and biological changes, including mass extinctions. Environmental changes caused by LIPs and SLIPs include rapid global warming, global cooling ('Snowball Earth'), oceanic anoxia events, mercury poisoning, atmospheric and oceanic acidification, and sea level changes. Continued research to characterize the effects of these extremely large and typically short duration igneous events on atmospheric and oceanic chemistry through Earth history can provide lessons for understanding and mitigating modern climate change. Large Igneous Provinces: A Driver of Global Environmental and Biotic Changes describes the interactions between the effects of LIPs and other drivers of climatic change, the limits of the LIP effect, and the atmospheric and oceanic consequences of LIPs in significant environmental events. Volume highlights include: Temporal record of large igneous provinces (LIPs) Environmental impacts of LIP emplacement Precambrian, Proterozoic, and Phanerozoic case histories Links between geochemical proxies and the LIP record Alternative causes for environmental change Key parameters related to LIPs and SLIPs for use in environmental change modelling Role of LIPs in Permo-Triassic, Triassic-Jurassic, and other mass extinction events The American Geophysical Union promotes discovery in Earth and space science for the benefit of humanity. Its publications disseminate scientific knowledge and provide resources for researchers, students, and professionals.


Interpreting the Difference in Magnitudes of PETM Carbon Isotope Excursions in Paleosol Carbonate and Paleosol Organic Matter

Interpreting the Difference in Magnitudes of PETM Carbon Isotope Excursions in Paleosol Carbonate and Paleosol Organic Matter

Author: Christopher Guy Cacciatore

Publisher:

Published: 2016

Total Pages: 78

ISBN-13:

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The Paleocene-Eocene Thermal Maximum (PETM) was a rapid global warming event at ~56 Ma that was driven by a rapid release of carbon into the ocean-atmosphere system. The most recognizable feature marking the PETM in the rock record is a negative carbon isotope excursion (CIE) recorded in organic carbon and calcium carbonates deposited in both marine and terrestrial environments. Differences among excursion magnitudes ([Delta]CIE) exist between marine and terrestrial proxies, and between carbonates and organic carbon. We evaluated the plausibility of two hypothetical mechanisms behind the observed ~ 1.9‰ difference between the magnitude of the CIE as recorded by paleosol carbonate and paleosol organic matter ([Delta]CIEpc-som). Specifically, we test whether 1) oxidation within soils of isotopically light methane or 2) increases in soil respiration rates are plausible explanations for the observed [Delta]CIE. A production-diffusion model used to simulate carbon isotope compositions of soil CO2 and paleosol carbonates is coupled with a box model that constrains methane flux from hydrates into atmosphere. The box model simulates atmospheric CO2 concentrations, the [delta]13C values of atmospheric CO2 and of plants, and the methane flux into soils, which are all used in the production-diffusion model to simulate the [delta]13C value of paleosol carbonate. Given conservative prior distributions for model inputs grounded in previous empirical studies, model output demonstrates that oxidation of atmospheric methane in soil pore space is unlikely to cause the [Delta]CIEpc-som even for rapid methane release rates. However, increased respiration rates during the PETM could explain the observed [Delta]CIE, with a minimum approximate doubling of respiration rates required to reproduce a [Delta]CIEpc-som ≥ 2‰.


Large Igneous Provinces

Large Igneous Provinces

Author: Richard E. Ernst

Publisher: Cambridge University Press

Published: 2014-09-25

Total Pages: 667

ISBN-13: 1316060519

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Large igneous provinces (LIPs) are intraplate magmatic events, involving volumes of mainly mafic magma upwards of 100,000 km3, and often above 1 million km3. They are linked to continental break-up, global environmental catastrophes, regional uplift and a variety of ore deposit types. In this up-to-date, fascinating book, leading expert Richard E. Ernst explores all aspects of LIPs, beginning by introducing their definition and essential characteristics. Topics covered include continental and oceanic LIPs; their origins, structures, and geochemistry; geological and environmental effects; association with silicic, carbonatite and kimberlite magmatism; and analogues of LIPs in the Archean, and on other planets. The book concludes with an assessment of LIPs' influence on natural resources such as mineral deposits, petroleum and aquifers. This is a one-stop resource for researchers and graduate students in a wide range of disciplines, including tectonics, igneous petrology, geochemistry, geophysics, Earth history, and planetary geology, and for mining industry professionals.


Ocean Acidification

Ocean Acidification

Author: National Research Council

Publisher: National Academies Press

Published: 2010-09-14

Total Pages: 200

ISBN-13: 030916155X

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The ocean has absorbed a significant portion of all human-made carbon dioxide emissions. This benefits human society by moderating the rate of climate change, but also causes unprecedented changes to ocean chemistry. Carbon dioxide taken up by the ocean decreases the pH of the water and leads to a suite of chemical changes collectively known as ocean acidification. The long term consequences of ocean acidification are not known, but are expected to result in changes to many ecosystems and the services they provide to society. Ocean Acidification: A National Strategy to Meet the Challenges of a Changing Ocean reviews the current state of knowledge, explores gaps in understanding, and identifies several key findings. Like climate change, ocean acidification is a growing global problem that will intensify with continued CO2 emissions and has the potential to change marine ecosystems and affect benefits to society. The federal government has taken positive initial steps by developing a national ocean acidification program, but more information is needed to fully understand and address the threat that ocean acidification may pose to marine ecosystems and the services they provide. In addition, a global observation network of chemical and biological sensors is needed to monitor changes in ocean conditions attributable to acidification.