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Dive into the research topics where Angela L. Coe is active.

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Featured researches published by Angela L. Coe.


Gsa Today | 2008

Are we now living in the Anthropocene

Jan Zalasiewicz; Mark Williams; Alan E. Smith; Tiffany L. Barry; Angela L. Coe; Paul R. Bown; Patrick J. Brenchley; David Cantrill; Andrew S. Gale; Philip L. Gibbard; F. John Gregory; Mark W. Hounslow; Andrew Craig Kerr; Paul Nicholas Pearson; Robert W. O'b. Knox; John H. Powell; Colin N. Waters; J. E. A. Marshall; Michael Oates; Peter F. Rawson; P. Stone

The term Anthropocene, proposed and increasingly employed to denote the current interval of anthropogenic global environmental change, may be discussed on stratigraphic grounds. A case can be made for its consideration as a formal epoch in that, since the start of the Industrial Revolution, Earth has endured changes sufficient to leave a global stratigraphic signature distinct from that of the Holocene or of previous Pleistocene interglacial phases, encompassing novel biotic, sedimentary, and geochemical change. These changes, although likely only in their initial phases, are sufficiently distinct and robustly established for suggestions of a Holocene–Anthropocene boundary in the recent historical past to be geologically reasonable. The boundary may be defined either via Global Stratigraphic Section and Point (“golden spike”) locations or by adopting a numerical date. Formal adoption of this term in the near future will largely depend on its utility, particularly to earth scientists working on late Holocene successions. This datum, from the perspective of the far future, will most probably approximate a distinctive stratigraphic boundary.


Nature | 2005

Astronomical pacing of methane release in the Early Jurassic period.

David B. Kemp; Angela L. Coe; Anthony S. Cohen; Lorenz Schwark

A pronounced negative carbon-isotope (δ13C) excursion of ∼5–7‰ (refs 1–7) indicates the occurrence of a significant perturbation to the global carbon cycle during the Early Jurassic period (early Toarcian age, ∼183 million years ago). The rapid release of 12C-enriched biogenic methane as a result of continental-shelf methane hydrate dissociation has been put forward as a possible explanation for this observation. Here we report high-resolution organic carbon-isotope data from well-preserved mudrocks in Yorkshire, UK, which demonstrate that the carbon-isotope excursion occurred in three abrupt stages, each showing a shift of -2‰ to -3‰. Spectral analysis of these carbon-isotope measurements and of high-resolution carbonate abundance data reveals a regular cyclicity. We interpret these results as providing strong evidence that methane release proceeded in three rapid pulses and that these pulses were controlled by astronomically forced changes in climate, superimposed upon longer-term global warming. We also find that the first two pulses of methane release each coincided with the extinction of a large proportion of marine species.


Geology | 2004

Osmium isotope evidence for the regulation of atmospheric CO2 by continental weathering

Anthony S. Cohen; Angela L. Coe; Stephen M. Harding; Lorenz Schwark

The long-term stability of Earth9s climate throughout the Phanerozoic stands in marked contrast to the dramatic fluctuations that have taken place on time scales as short as a few years, reflecting the high efficiency of longer-term climate regulation through negative feedbacks. A fundamental mechanism is thought to involve control of CO 2 in the ocean- atmosphere system through continental weathering, although unambiguous, high-resolution data supporting this hypothesis have hitherto not been available. Organic-rich mud rocks from Yorkshire, England, which were deposited during the Toarcian oceanic anoxic event (ca. 181 Ma, Early Jurassic), contain evidence of an exceptionally large excursion in the 187 Os/ 188 Os ratio of contemporaneous seawater, from ∼0.4 to ∼1.0. The most likely explanation for this excursion is that it resulted from a transient increase in global continental weathering rates of ∼400%–800%. The Os isotope excursion coincided with a well-documented global δ 13 C excursion of −6‰ that affected all the major biospheric reservoirs of the time. Higher mean global temperatures caused global chemical weathering rates to increase substantially, while, in turn, chemical weathering was very effective in reducing the elevated levels of atmospheric CO 2 and the high temperatures to preexcursion levels.


Geochimica et Cosmochimica Acta | 1994

STRONTIUM ISOTOPIC VARIATIONS IN JURASSIC AND CRETACEOUS SEAWATER

Charles E Jones; Hugh C. Jenkyns; Angela L. Coe; Hesselbo P Stephen

A high-resolution seawater strontium isotope curve has been generated through the analysis of well-dated and well-preserved belemnites and oysters from the Middle and Upper Jurassic and the Lower Cretaceous of Great Britain. Analysis of Fe and Mn concentrations in these fossils has yielded criteria for eliminating samples that are diagenetically altered. The strontium isotope curve remains relatively flat through the Aalenian and early Bajocian, rapidly descends through the late Bajocian and Bathonian, and reaches a minimum in the Callovian and Oxfordian. It then begins a rapid increase in the Kimmeridgian and Portlandian that continues through much of the early Cretaceous. The curve levels off in the Barremian, suddenly dips downwards in the Aptian, and recovers gradually through the Albian. The strontium isotopic variations are sufficiently large and the data are presented with sufficient stratigraphic detail to allow precise correlation to the classic ammonite zones and lithologic sections of Great Britain using the techniques of strontium isotope stratigraphy. Model results indicate that much of the variation in seawater 87Sr86Sr between 120 and 40 Ma can be explained by changing the intensity of mid-ocean ridge hydrothermal fluxes proportionally to estimated mid-ocean ridge crustal generation rates. It is also possible that the variations during the rest of the Mesozoic and the Permian are primarily reflections of changing hydrothermal inputs. The model results have several important implications. First, they provide an example in which the variations in the strontium isotope curve are not necessarily driven by changes in fluvial inputs. Second, they suggest that from at least the Aptian through the Eocene variations in continental weathering were minimal. This heightens the importance of the rapid rise in seawater 87Sr86Sr beginning ~ 40 Ma as a significant transition to an extended period of increasing fluvial 87Sr fluxes continuing to the present. Finally, the results suggest that several documented short-term excursions towards lower 87Sr86Sr in the latest Triassic, Pliensbachian-Toarcian, Callovian-Oxfordian, Aptian-Albian, and Cenomanian-Turonian are interpretable as pulses of seafloor hydrothermal activity. If so, the strontium isotope record offers a means of constraining the timing, duration, and magnitude of known or proposed hydrothermal events in the geological record.


Earth and Planetary Science Letters | 1999

Precise Re–Os ages of organic-rich mudrocks and the Os isotope composition of Jurassic seawater

Anthony S. Cohen; Angela L. Coe; Jessica M. Bartlett; Chris J. Hawkesworth

Rhenium and osmium isotope and abundance data have been obtained on precisely-located samples from three suites of immature, organic-rich mudrocks from Jurassic coastal outcrops in England. The data provide accurate whole-rock ages of 207±12 Ma, 181±13 Ma and 155±4.3 Ma for suites of Hettangian, Toarcian (exaratum Subzone) and Kimmeridgian (sensu anglico, wheatleyensis Subzone) samples. These new Re–Os ages are indistinguishable, within the assigned analytical uncertainties, from interpolated depositional ages estimated from published geological timescales, and establish the importance of the Re–Os dating technique for chronostratigraphic studies. Early-diagenetic pyrite nodules possess levels of Re and Os which are ∼1–2 orders of magnitude lower than in the enclosing organic-rich mudrocks, indicating that these elements had already been removed from sediment pore waters at the time of nodule formation. Thus the Re–Os isotope system in these organic-rich mudrocks has been closed since, or from very soon after, the time of sediment deposition. Because most of the Re (98+%) and Os (95–99.8+%) in the mudrocks is shown to be hydrogenous, the 187Os/188Os(i) of the samples is interpreted to be that of contemporaneous seawater. The data thereby provide the first estimates of the Os isotope composition of Jurassic seawater. During the earliest Jurassic (Hettangian), the seawater 187Os/188Os ratio was extremely unradiogenic (∼0.15); it had increased to ∼0.8 at the end of the Early Jurassic (Toarcian) ∼20 Ma later, while in the Late Jurassic (Kimmeridgian) the seawater 187Os/188Os ratio was ∼0.59. The most likely explanation for the unradiogenic Os isotope composition of Hettangian seawater is that the contribution of unradiogenic Os to the oceans from the hydrothermal alteration of oceanic crust greatly exceeded the input of radiogenic Os from the continents at that time. This interpretation is in line with observations suggesting that global weathering rates were low in the Hettangian, and that increased hydrothermal and volcanic activity preceded the break-up of Pangea. The Re/Os ratios of Hettangian mudrocks (and by inference, of contemporaneous seawater) are similar to those of mudrocks deposited at later times during the Jurassic, and argues against the unradiogenic Os in Hettangian seawater being derived from extraterrestrial meteoritic sources.


Geology | 2008

Molybdenum isotope evidence for global ocean anoxia coupled with perturbations to the carbon cycle during the Early Jurassic

Christopher R. Pearce; Anthony S. Cohen; Angela L. Coe; Kevin W. Burton

Relatively brief periods of severe paleoenvironmental change during the Jurassic and Cretaceous were associated with the widespread accumulation of organic-rich marine deposits, termed oceanic anoxic events (OAEs). These intervals involved abrupt global warming of ∼5–10 °C, higher rates of continental weathering, elevated extinction rates, and large-scale perturbations to the global carbon cycle. The major OAEs also overlapped temporally the emplacement of large igneous provinces. However, despite being known as OAEs, the extent of seawater anoxia at those times is undefined and the causative processes remain unclear. Here we show how changes in seawater molybdenum isotope ratios (a proxy for seawater anoxia) during the Toarcian (Early Jurassic) OAE define the onset and expansion of oxygen deficient conditions. Our data also place constraints on the areal extent of marine anoxia during the event and demonstrate that anoxia expanded and contracted periodically, broadly in line with precession-driven changes in δ13 Corg. Despite their intermittent occurrence over geological history, OAEs have an important contemporary relevance because the magnitude and high rates of environmental change then were broadly similar to those occurring at the present day.


Journal of the Geological Society | 2007

The Late Palaeocene–Early Eocene and Toarcian (Early Jurassic) carbon isotope excursions: a comparison of their time scales, associated environmental changes, causes and consequences

Anthony S. Cohen; Angela L. Coe; David B. Kemp

Although the Earths environment is constantly changing, there have been a few unusual episodes over the last c. 200 Ma when change was extreme in terms of its rapidity, severity, long-lasting consequences and unpredictability. The geochemical and biotic records for two of these episodes, the Palaeocene–Eocene thermal maximum and the Toarcian Oceanic Anoxic Event (Early Jurassic), possess many significant similarities. Each event was associated with a major carbon isotope excursion, significant levels of biotic extinctions, severe global warming, an enhanced hydrological cycle, and evidence for widespread seawater anoxia. Both carbon isotope excursions can be subdivided into distinct stages with broadly similar characteristics and durations; based on a detailed comparison, the Palaeocene–Eocene thermal maximum may have been an incipient Oceanic Anoxic Event. The geochemical and biotic changes during these two events are most readily explained by the abrupt, large-scale dissociation of methane hydrate that followed a period of more gradual environmental change linked to the emplacement of a large igneous province. Carbon release rates at those times were of the same order of magnitude as the current anthropogenic release rate of carbon to the atmosphere, indicating that ancient events such as these may usefully serve as analogues for present-day environmental change.


Philosophical Transactions of the Royal Society A | 2011

Stratigraphy of the Anthropocene

Jan Zalasiewicz; Mark Williams; R Fortey; Alan E. Smith; Tiffany L. Barry; Angela L. Coe; Paul R. Bown; Peter F. Rawson; Andrew S. Gale; Philip L. Gibbard; Fj Gregory; Mark W. Hounslow; Andrew Craig Kerr; Paul Nicholas Pearson; Robert W. O'b. Knox; John H. Powell; Colin N. Waters; J. E. A. Marshall; Michael Oates; P. Stone

The Anthropocene, an informal term used to signal the impact of collective human activity on biological, physical and chemical processes on the Earth system, is assessed using stratigraphic criteria. It is complex in time, space and process, and may be considered in terms of the scale, relative timing, duration and novelty of its various phenomena. The lithostratigraphic signal includes both direct components, such as urban constructions and man-made deposits, and indirect ones, such as sediment flux changes. Already widespread, these are producing a significant ‘event layer’, locally with considerable long-term preservation potential. Chemostratigraphic signals include new organic compounds, but are likely to be dominated by the effects of CO2 release, particularly via acidification in the marine realm, and man-made radionuclides. The sequence stratigraphic signal is negligible to date, but may become geologically significant over centennial/millennial time scales. The rapidly growing biostratigraphic signal includes geologically novel aspects (the scale of globally transferred species) and geologically will have permanent effects.


Geology | 2002

New geochemical evidence for the onset of volcanism in the Central Atlantic magmatic province and environmental change at the Triassic-Jurassic boundary

Anthony S. Cohen; Angela L. Coe

The Late Triassic–Early Jurassic was a time of major global change; however, the fundamental processes driving these changes are less than clear. We have determined the Re and Os abundances, and Os isotope compositions, of marine mudrock samples that span the Triassic-Jurassic boundary in the UK and have established that major isotopic and geochemical shifts in the composition of seawater took place in the latest Triassic. We argue that these shifts were caused by the sudden initiation of widespread igneous activity within the Central Atlantic magmatic province, associated with rifting of the supercontinent Pangea. The Os isotope composition of seawater responded rapidly to these events, demonstrating that the seawater Os isotope system has great potential in identifying the nature and precise timing of major environmental change.


Philosophical Transactions of the Royal Society A | 1999

Astronomical calibration of the Jurassic time-scale from cyclostratigraphy in British mudrock formations

Graham P. Weedon; Hugh C. Jenkyns; Angela L. Coe; Stephen P. Hesselbo

Three British Jurassic mudrock formations have been investigated, via time–series analysis, for evidence of sedimentary cyclicity related to orbital–climatic (Milankovitch) cyclicity: the Blue Lias, the Belemnite Marls and the Kimmeridge Clay Formation. Magnetic–susceptibility measurements through the Blue Lias (uppermost Triassic to Sinemurian) were used to generate high–resolution time–series. The data indicate the presence of a regular sedimentary cycle that gradually varies in wavelength according to sedimentation rate. Tuning of this cycle to the 38ka Jurassic obliquity cycle produces spectral evidence for two additional regular cycles of small amplitude. These correspond to the 95 ka component of orbital eccentricity and the 20 ka orbital–precession cycles. Cycle counting allowed the minimum duration of four ammonite zones to be estimated and the duration of the Hettangian stage is estimated to be at least 1.29 Ma. Calcium carbonate measurements through the Belemnite Marls (lower Pliensbachian) are characterized by two scales of cyclicity that can be firmly linked to orbital–precession (20 ka) and the 123 ka component of eccentricity. A time–scale has been developed from the precession–related sedimentary cycles, with cycle counts used to constrain the duration of two ammonite zones. In the Kimmeridge Clay Formation (Kimmeridgian–Tithonian), magnetic–susceptibility measurements made on exposures, core material and down boreholes can be correlated at the decimetre scale. Only measurements of magnetic susceptibility made below the Yellow Ledge Stone Band (midway through the formation) are suitable for analysis of the bedding–scale cyclicity. A large–amplitude sedimentary cycle detected in the lower part of the formation is probably related to the orbital–obliquity cycle (38 ka). In certain stratigraphic intervals, there is evidence for small–amplitude cycles related to orbital precession (20 ka). This study of the British Jurassic shows that, in the Rhaetian–Sinemurian, the dominant cyclicity was related to obliquity. In the Pliensbachian this had shifted to dominantly precession, and in the Kimmeridgian obliquity again dominated. These shifts in cycle dominance presumably reflect changing local or global palaeoclimatic and/or palaeoceanographic conditions.

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Graham P. Weedon

University of Bedfordshire

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Colin N. Waters

British Geological Survey

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J. E. A. Marshall

National Oceanography Centre

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