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  • 1
    Publication Date: 2008-08-30
    Description: It is thought that the Northern Hemisphere experienced only ephemeral glaciations from the Late Eocene to the Early Pliocene epochs (about 38 to 4 million years ago), and that the onset of extensive glaciations did not occur until about 3 million years ago. Several hypotheses have been proposed to explain this increase in Northern Hemisphere glaciation during the Late Pliocene. Here we use a fully coupled atmosphere-ocean general circulation model and an ice-sheet model to assess the impact of the proposed driving mechanisms for glaciation and the influence of orbital variations on the development of the Greenland ice sheet in particular. We find that Greenland glaciation is mainly controlled by a decrease in atmospheric carbon dioxide during the Late Pliocene. By contrast, our model results suggest that climatic shifts associated with the tectonically driven closure of the Panama seaway, with the termination of a permanent El Nino state or with tectonic uplift are not large enough to contribute significantly to the growth of the Greenland ice sheet; moreover, we find that none of these processes acted as a priming mechanism for glacial inception triggered by variations in the Earth's orbit.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lunt, Daniel J -- Foster, Gavin L -- Haywood, Alan M -- Stone, Emma J -- England -- Nature. 2008 Aug 28;454(7208):1102-5. doi: 10.1038/nature07223.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉BRIDGE, School of Geographical Sciences, University of Bristol, University Road, Bristol BS8 1SS, UK. d.j.lunt@bristol.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18756254" target="_blank"〉PubMed〈/a〉
    Keywords: Atmosphere/*chemistry ; Carbon Dioxide/analysis/*metabolism ; Climate ; Greenland ; History, Ancient ; *Ice Cover ; North America ; Rain ; Time Factors
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    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2009-03-28
    Description: Rivers are the dominant source of many elements and isotopes to the ocean. But this input from the continents is not balanced by the loss of the elements and isotopes through hydrothermal and sedimentary exchange with the oceanic crust, or by temporal changes in the marine inventory for elements that are demonstrably not in steady state. To resolve the problem of the observed imbalance in marine geochemical budgets, attention has been focused on uncertainties in the hydrothermal and sedimentary fluxes. In recent Earth history, temporally dynamic chemical weathering fluxes from the continents are an inevitable consequence of periodic glaciations. Chemical weathering rates on modern Earth are likely to remain far from equilibrium owing to the physical production of finely ground material at glacial terminations that acts as a fertile substrate for chemical weathering. Here we explore the implications of temporal changes in the riverine chemical weathering flux for oceanic geochemical budgets. We contend that the riverine flux obtained from observations of modern rivers is broadly accurate, but not representative of timescales appropriate for elements with oceanic residence longer than Quaternary glacial-interglacial cycles. We suggest that the pulse of rapid chemical weathering initiated at the last deglaciation has not yet decayed away and that weathering rates remain about two to three times the average for an entire late Quaternary glacial cycle. Taking into account the effect of the suggested non-steady-state process on the silicate weathering flux helps to reconcile the modelled marine strontium isotope budget with available data. Overall, we conclude that consideration of the temporal variability in riverine fluxes largely ameliorates long-standing problems with chemical and isotopic mass balances in the ocean.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vance, Derek -- Teagle, Damon A H -- Foster, Gavin L -- England -- Nature. 2009 Mar 26;458(7237):493-6. doi: 10.1038/nature07828.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Bristol Isotope Group, Department of Earth Sciences, University of Bristol, Wills Memorial Building, Bristol BS8 1RJ, UK. d.vance@bristol.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19325631" target="_blank"〉PubMed〈/a〉
    Keywords: Atmosphere/chemistry ; Carbon Dioxide/analysis ; Carbonates/analysis/chemistry ; Geologic Sediments/*chemistry ; History, Ancient ; Ice Cover ; Osmium/analysis ; Rivers/*chemistry ; Seawater/*chemistry ; Strontium/analysis/chemistry ; Strontium Isotopes ; Temperature
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  • 3
    Publication Date: 2009-09-15
    Description: Geological and geochemical evidence indicates that the Antarctic ice sheet formed during the Eocene-Oligocene transition, 33.5-34.0 million years ago. Modelling studies suggest that such ice-sheet formation might have been triggered when atmospheric carbon dioxide levels (pCO2atm) fell below a critical threshold of approximately 750 p.p.m.v., but the timing and magnitude of pCO2atm relative to the evolution of the ice sheet has remained unclear. Here we use the boron isotope pH proxy on exceptionally well-preserved carbonate microfossils from a recently discovered geological section in Tanzania to estimate pCO2atm before, during and after the climate transition. Our data suggest that are reduction in pCO2atm occurred before the main phase of ice growth,followed by a sharp recovery to pre-transition values and then a more gradual decline. During maximum ice-sheet growth, pCO2atm was between approximately 450 and approximately 1,500 p.p.m.v., with a central estimate of approximately 760 p.p.m.v. The ice cap survived the period of pCO2atm recovery,although possibly with some reduction in its volume, implying (as models predict) a nonlinear response to climate forcing during melting. Overall, our results confirm the central role of declining pCO2atm in the development of the Antarctic ice sheet (in broad agreement with carbon cycle modelling) and help to constrain mechanisms and feedbacks associated with the Earth's biggest climate switch of the past 65 Myr.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pearson, Paul N -- Foster, Gavin L -- Wade, Bridget S -- England -- Nature. 2009 Oct 22;461(7267):1110-3. doi: 10.1038/nature08447. Epub 2009 Sep 13.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉School of Earth and Ocean Sciences, Cardiff University, Cardiff CF10 3YE, UK. pearsonp@cardiff.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19749741" target="_blank"〉PubMed〈/a〉
    Keywords: Antarctic Regions ; Atmosphere/*chemistry ; Boron ; Carbon Dioxide/*analysis ; *Climate ; Foraminifera/chemistry ; Fossils ; History, Ancient ; Hydrogen-Ion Concentration ; Ice Cover/chemistry ; Isotopes ; Plankton/chemistry ; Seawater/chemistry ; Sensitivity and Specificity ; Tanzania ; Temperature
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    Electronic ISSN: 1476-4687
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  • 4
    Publication Date: 2015-08-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Martinez-Boti, M A -- Foster, G L -- Chalk, T B -- Rohling, E J -- Sexton, P F -- Lunt, D J -- Pancost, R D -- Badger, M P S -- Schmidt, D N -- England -- Nature. 2015 Oct 15;526(7573):458. doi: 10.1038/nature14954. Epub 2015 Aug 19.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/26287457" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
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  • 5
    Publication Date: 2015-02-06
    Description: Theory and climate modelling suggest that the sensitivity of Earth's climate to changes in radiative forcing could depend on the background climate. However, palaeoclimate data have thus far been insufficient to provide a conclusive test of this prediction. Here we present atmospheric carbon dioxide (CO2) reconstructions based on multi-site boron-isotope records from the late Pliocene epoch (3.3 to 2.3 million years ago). We find that Earth's climate sensitivity to CO2-based radiative forcing (Earth system sensitivity) was half as strong during the warm Pliocene as during the cold late Pleistocene epoch (0.8 to 0.01 million years ago). We attribute this difference to the radiative impacts of continental ice-volume changes (the ice-albedo feedback) during the late Pleistocene, because equilibrium climate sensitivity is identical for the two intervals when we account for such impacts using sea-level reconstructions. We conclude that, on a global scale, no unexpected climate feedbacks operated during the warm Pliocene, and that predictions of equilibrium climate sensitivity (excluding long-term ice-albedo feedbacks) for our Pliocene-like future (with CO2 levels up to maximum Pliocene levels of 450 parts per million) are well described by the currently accepted range of an increase of 1.5 K to 4.5 K per doubling of CO2.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Martinez-Boti, M A -- Foster, G L -- Chalk, T B -- Rohling, E J -- Sexton, P F -- Lunt, D J -- Pancost, R D -- Badger, M P S -- Schmidt, D N -- England -- Nature. 2015 Feb 5;518(7537):49-54. doi: 10.1038/nature14145.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Ocean and Earth Science, University of Southampton, National Oceanography Centre Southampton, Southampton, SO14 3ZH, UK. ; 1] Ocean and Earth Science, University of Southampton, National Oceanography Centre Southampton, Southampton, SO14 3ZH, UK [2] Research School of Earth Sciences, The Australian National University, Canberra, Australian Capital Territory 2601, Australia. ; Centre for Earth, Planetary, Space and Astronomical Research, The Open University, Milton Keynes, MK7 6AA, UK. ; 1] School of Geographical Sciences, University of Bristol, University Road, Bristol, BS8 1SS, UK [2] The Cabot Institute, University of Bristol, Bristol BS8 1UJ, UK. ; 1] The Cabot Institute, University of Bristol, Bristol BS8 1UJ, UK [2] Organic Geochemistry Unit, School of Chemistry, University of Bristol, Bristol BS8 1TS, UK. ; 1] The Cabot Institute, University of Bristol, Bristol BS8 1UJ, UK [2] School of Earth Sciences, University of Bristol, Wills Memorial Building, Bristol, BS8 1RJ, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25652996" target="_blank"〉PubMed〈/a〉
    Keywords: Atmosphere/chemistry ; Boron/analysis/chemistry ; Carbon Dioxide/*analysis ; *Climate ; *Feedback ; Foraminifera/metabolism ; Geologic Sediments/chemistry ; History, Ancient ; Hydrogen-Ion Concentration ; Ice Cover ; Oceans and Seas ; Oxygen Isotopes ; Temperature ; Time Factors
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    Electronic ISSN: 1476-4687
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  • 6
    Publication Date: 2015-02-13
    Description: Atmospheric CO2 fluctuations over glacial-interglacial cycles remain a major challenge to our understanding of the carbon cycle and the climate system. Leading hypotheses put forward to explain glacial-interglacial atmospheric CO2 variations invoke changes in deep-ocean carbon storage, probably modulated by processes in the Southern Ocean, where much of the deep ocean is ventilated. A central aspect of such models is that, during deglaciations, an isolated glacial deep-ocean carbon reservoir is reconnected with the atmosphere, driving the atmospheric CO2 rise observed in ice-core records. However, direct documentation of changes in surface ocean carbon content and the associated transfer of carbon to the atmosphere during deglaciations has been hindered by the lack of proxy reconstructions that unambiguously reflect the oceanic carbonate system. Radiocarbon activity tracks changes in ocean ventilation, but not in ocean carbon content, whereas proxies that record increased deglacial upwelling do not constrain the proportion of upwelled carbon that is degassed relative to that which is taken up by the biological pump. Here we apply the boron isotope pH proxy in planktic foraminifera to two sediment cores from the sub-Antarctic Atlantic and the eastern equatorial Pacific as a more direct tracer of oceanic CO2 outgassing. We show that surface waters at both locations, which partly derive from deep water upwelled in the Southern Ocean, became a significant source of carbon to the atmosphere during the last deglaciation, when the concentration of atmospheric CO2 was increasing. This oceanic CO2 outgassing supports the view that the ventilation of a deep-ocean carbon reservoir in the Southern Ocean had a key role in the deglacial CO2 rise, although our results allow for the possibility that processes operating in other regions may also have been important for the glacial-interglacial ocean-atmosphere exchange of carbon.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Martinez-Boti, M A -- Marino, G -- Foster, G L -- Ziveri, P -- Henehan, M J -- Rae, J W B -- Mortyn, P G -- Vance, D -- England -- Nature. 2015 Feb 12;518(7538):219-22. doi: 10.1038/nature14155.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Ocean and Earth Science, National Oceanography Centre Southampton, University of Southampton Waterfront Campus, Southampton SO14 3ZH, UK. ; 1] Institute of Environmental Science and Technology (ICTA), Universitat Autonoma de Barcelona, Bellaterra, Catalonia, 08193, Spain [2] Research School of Earth Sciences, The Australian National University, Canberra, Australian Capital Territory 2601, Australia. ; 1] Institute of Environmental Science and Technology (ICTA), Universitat Autonoma de Barcelona, Bellaterra, Catalonia, 08193, Spain [2] Institucio Catalana de Recerca i Estudis Avancats, ICREA, Barcelona, Catalonia, 08010, Spain [3] Earth and Climate Cluster, Department of Earth Sciences, Faculty of Earth and Life Sciences, VU Universiteit Amsterdam, 1081HV Amsterdam, The Netherlands. ; 1] Ocean and Earth Science, National Oceanography Centre Southampton, University of Southampton Waterfront Campus, Southampton SO14 3ZH, UK [2] Department of Geology and Geophysics, Yale University, New Haven, Connecticut 06511, USA. ; 1] Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, California 91125, USA [2] Department of Earth and Environmental Sciences, University of St Andrews, St Andrews KY16 9AL, UK. ; 1] Institute of Environmental Science and Technology (ICTA), Universitat Autonoma de Barcelona, Bellaterra, Catalonia, 08193, Spain [2] Department of Geography, Universitat Autonoma de Barcelona, Bellaterra, Catalonia, 08193, Spain. ; Institute of Geochemistry and Petrology, Department of Earth Sciences, ETH Zurich, NW D81.4, Zurich 8092, Switzerland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25673416" target="_blank"〉PubMed〈/a〉
    Keywords: Atmosphere/chemistry ; Boron/*analysis/*chemistry ; Carbon Dioxide/*analysis ; Climate ; Foraminifera ; Freezing ; History, Ancient ; Hydrogen-Ion Concentration ; Ice Cover/*chemistry ; Isotopes ; Oceans and Seas ; Seawater/*chemistry
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  • 7
    Publication Date: 2012-03-03
    Description: Ocean acidification may have severe consequences for marine ecosystems; however, assessing its future impact is difficult because laboratory experiments and field observations are limited by their reduced ecologic complexity and sample period, respectively. In contrast, the geological record contains long-term evidence for a variety of global environmental perturbations, including ocean acidification plus their associated biotic responses. We review events exhibiting evidence for elevated atmospheric CO(2), global warming, and ocean acidification over the past ~300 million years of Earth's history, some with contemporaneous extinction or evolutionary turnover among marine calcifiers. Although similarities exist, no past event perfectly parallels future projections in terms of disrupting the balance of ocean carbonate chemistry-a consequence of the unprecedented rapidity of CO(2) release currently taking place.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Honisch, Barbel -- Ridgwell, Andy -- Schmidt, Daniela N -- Thomas, Ellen -- Gibbs, Samantha J -- Sluijs, Appy -- Zeebe, Richard -- Kump, Lee -- Martindale, Rowan C -- Greene, Sarah E -- Kiessling, Wolfgang -- Ries, Justin -- Zachos, James C -- Royer, Dana L -- Barker, Stephen -- Marchitto, Thomas M Jr -- Moyer, Ryan -- Pelejero, Carles -- Ziveri, Patrizia -- Foster, Gavin L -- Williams, Branwen -- New York, N.Y. -- Science. 2012 Mar 2;335(6072):1058-63. doi: 10.1126/science.1208277.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Lamont-Doherty Earth Observatory of Columbia University, Palisades, NY 10964, USA. hoenisch@ldeo.columbia.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22383840" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptation, Biological ; Animals ; *Aquatic Organisms ; Atmosphere ; Carbon Dioxide ; Carbonates/analysis ; *Ecosystem ; Extinction, Biological ; Forecasting ; Fossils ; *Geological Phenomena ; Hydrogen-Ion Concentration ; Oceans and Seas ; Seawater/*chemistry
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 8
    Publication Date: 2014-04-18
    Description: Ice volume (and hence sea level) and deep-sea temperature are key measures of global climate change. Sea level has been documented using several independent methods over the past 0.5 million years (Myr). Older periods, however, lack such independent validation; all existing records are related to deep-sea oxygen isotope (delta(18)O) data that are influenced by processes unrelated to sea level. For deep-sea temperature, only one continuous high-resolution (Mg/Ca-based) record exists, with related sea-level estimates, spanning the past 1.5 Myr. Here we present a novel sea-level reconstruction, with associated estimates of deep-sea temperature, which independently validates the previous 0-1.5 Myr reconstruction and extends it back to 5.3 Myr ago. We find that deep-sea temperature and sea level generally decreased through time, but distinctly out of synchrony, which is remarkable given the importance of ice-albedo feedbacks on the radiative forcing of climate. In particular, we observe a large temporal offset during the onset of Plio-Pleistocene ice ages, between a marked cooling step at 2.73 Myr ago and the first major glaciation at 2.15 Myr ago. Last, we tentatively infer that ice sheets may have grown largest during glacials with more modest reductions in deep-sea temperature.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rohling, E J -- Foster, G L -- Grant, K M -- Marino, G -- Roberts, A P -- Tamisiea, M E -- Williams, F -- England -- Nature. 2014 Apr 24;508(7497):477-82. doi: 10.1038/nature13230. Epub 2014 Apr 16.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉1] Research School of Earth Sciences, The Australian National University, Canberra 0200, Australia [2] Ocean and Earth Science, University of Southampton, National Oceanography Centre, Southampton SO14 3ZH, UK. ; Ocean and Earth Science, University of Southampton, National Oceanography Centre, Southampton SO14 3ZH, UK. ; Research School of Earth Sciences, The Australian National University, Canberra 0200, Australia. ; National Oceanography Centre, Joseph Proudman Building, Liverpool L3 5DA, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24739960" target="_blank"〉PubMed〈/a〉
    Keywords: Foraminifera ; History, Ancient ; Ice Cover ; Mediterranean Sea ; Oxygen Isotopes ; Reproducibility of Results ; Seawater/*analysis ; *Temperature ; Time Factors
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    Electronic ISSN: 1476-4687
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  • 9
    Publication Date: 2012-08-31
    Description: Atmospheric carbon dioxide concentrations and climate are regulated on geological timescales by the balance between carbon input from volcanic and metamorphic outgassing and its removal by weathering feedbacks; these feedbacks involve the erosion of silicate rocks and organic-carbon-bearing rocks. The integrated effect of these processes is reflected in the calcium carbonate compensation depth, which is the oceanic depth at which calcium carbonate is dissolved. Here we present a carbonate accumulation record that covers the past 53 million years from a depth transect in the equatorial Pacific Ocean. The carbonate compensation depth tracks long-term ocean cooling, deepening from 3.0-3.5 kilometres during the early Cenozoic (approximately 55 million years ago) to 4.6 kilometres at present, consistent with an overall Cenozoic increase in weathering. We find large superimposed fluctuations in carbonate compensation depth during the middle and late Eocene. Using Earth system models, we identify changes in weathering and the mode of organic-carbon delivery as two key processes to explain these large-scale Eocene fluctuations of the carbonate compensation depth.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Palike, Heiko -- Lyle, Mitchell W -- Nishi, Hiroshi -- Raffi, Isabella -- Ridgwell, Andy -- Gamage, Kusali -- Klaus, Adam -- Acton, Gary -- Anderson, Louise -- Backman, Jan -- Baldauf, Jack -- Beltran, Catherine -- Bohaty, Steven M -- Bown, Paul -- Busch, William -- Channell, Jim E T -- Chun, Cecily O J -- Delaney, Margaret -- Dewangan, Pawan -- Dunkley Jones, Tom -- Edgar, Kirsty M -- Evans, Helen -- Fitch, Peter -- Foster, Gavin L -- Gussone, Nikolaus -- Hasegawa, Hitoshi -- Hathorne, Ed C -- Hayashi, Hiroki -- Herrle, Jens O -- Holbourn, Ann -- Hovan, Steve -- Hyeong, Kiseong -- Iijima, Koichi -- Ito, Takashi -- Kamikuri, Shin-ichi -- Kimoto, Katsunori -- Kuroda, Junichiro -- Leon-Rodriguez, Lizette -- Malinverno, Alberto -- Moore, Ted C Jr -- Murphy, Brandon H -- Murphy, Daniel P -- Nakamura, Hideto -- Ogane, Kaoru -- Ohneiser, Christian -- Richter, Carl -- Robinson, Rebecca -- Rohling, Eelco J -- Romero, Oscar -- Sawada, Ken -- Scher, Howie -- Schneider, Leah -- Sluijs, Appy -- Takata, Hiroyuki -- Tian, Jun -- Tsujimoto, Akira -- Wade, Bridget S -- Westerhold, Thomas -- Wilkens, Roy -- Williams, Trevor -- Wilson, Paul A -- Yamamoto, Yuhji -- Yamamoto, Shinya -- Yamazaki, Toshitsugu -- Zeebe, Richard E -- England -- Nature. 2012 Aug 30;488(7413):609-14. doi: 10.1038/nature11360.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Ocean and Earth Science, National Oceanography Centre Southampton, University of Southampton, Waterfront Campus, European Way, Southampton SO14 3ZH, UK. hpaelike@marum.de〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22932385" target="_blank"〉PubMed〈/a〉
    Keywords: *Altitude ; Atmosphere/chemistry ; Calcium Carbonate/*analysis ; *Carbon Cycle ; Carbon Dioxide/analysis ; Diatoms/metabolism ; Foraminifera/metabolism ; Geologic Sediments/chemistry ; Global Warming/history/statistics & numerical data ; History, 21st Century ; History, Ancient ; Marine Biology ; Oxygen/metabolism ; Pacific Ocean ; Seawater/*chemistry ; Temperature
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    Electronic ISSN: 1476-4687
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  • 10
    Publication Date: 2007-02-17
    Description: Granitic plutonism is the principal agent of crustal differentiation, but linking granite emplacement to crust formation requires knowledge of the magmatic evolution, which is notoriously difficult to reconstruct from bulk rock compositions. We unlocked the plutonic archive through hafnium (Hf) and oxygen (O) isotope analysis of zoned zircon crystals from the classic hornblende-bearing (I-type) granites of eastern Australia. This granite type forms by the reworking of sedimentary materials by mantle-like magmas instead of by remelting ancient metamorphosed igneous rocks as widely believed. I-type magmatism thus drives the coupled growth and differentiation of continental crust.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kemp, A I S -- Hawkesworth, C J -- Foster, G L -- Paterson, B A -- Woodhead, J D -- Hergt, J M -- Gray, C M -- Whitehouse, M J -- New York, N.Y. -- Science. 2007 Feb 16;315(5814):980-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Bristol Isotope Group, Earth Sciences Department, University of Bristol, Bristol BS8 1RJ, UK. tony.kemp@jcu.edu.au〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17303751" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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