Andrey V Korsakov

Andrey V Korsakov

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Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 April 2001 in Contributions to Mineralogy and Petrology
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JHJörg Hermann
Jörg Hermann
DRDaniela Rubatto
Daniela Rubatto
AKAndrey V Korsakov
Andrey V Korsakov
VSVladislav S. Shatsky
Vladislav S. Shatsky

1 January 2006 in Earth and Planetary Science Letters
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Journal Article
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AKAndrey V Korsakov
Andrey V Korsakov
JHJörg Hermann
Jörg Hermann

1 April 2018 in Chemical Geology
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Journal Article
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AGAlexander V. Golovin
Alexander V. Golovin
ISIgor Sharygin
Igor Sharygin
VKVadim Kamenetsky
Vadim Kamenetsky
AKAndrey V Korsakov
Andrey V Korsakov
GYGregory M. Yaxley
Gregory M. Yaxley

17 June 2009 in Journal of the Geological Society
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HMHorst R. Marschall
Horst R. Marschall
AKAndrey V Korsakov
Andrey V Korsakov
GLGeorge Luiz Luvizotto
George Luiz Luvizotto
LNLutz Nasdala
Lutz Nasdala
TLThomas Ludwig
Thomas Ludwig
The extensive P–T stability and the high chemical variability of tourmaline (Tur) together with its common occurrence in metasediments proves its high potential for petrological and (isotope) geochemical studies on fluid–rock interaction in subduction- and collision-related rocks. This paper reviews the occurrence, major element chemistry and boron isotopic composition of Tur in high- and ultrahigh-pressure metamorphic (UHPM) rocks. In addition, it presents a new discovery of coesite-bearing Tur (schorl) from the Erzgebirge (Germany), as well as Tur (dravite) related to the retrograde history of coesite- and diamond-bearing rocks from the Erzgebirge and the Kokchetav Massif (Kazakhstan). The scarce data on worldwide occurrences of (U)HPM Tur reveal a high occupation of the crystallographic X-site (dominated by Na) and the possible presence of excess B, with little further distinctiveness in its major element composition when compared with Tur from medium-grade rocks. High K 2 O contents in Tur are probably not related to UHP growth or equilibration. The B isotopic composition of (U)HPM Tur ranges in δ 11 B from −16 to +1‰, with many samples in or below the range of continental crust. In contrast, Tur formed during retrograde fluid influx typically shows high δ 11 B values (up to +28‰), suggesting heavy-B fluids infiltrating the exhuming (U)HPM units. Coesite inclusions in Tur, characterized by Raman spectroscopy, are regarded as the best indicator for its UHP stability. Supplementary material: Analytical methods, tourmaline compositions and boron isotope values are available at http://www.geolsoc.org.uk/SUP18354 .

28 October 2019 in Geology
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Matteo AlvaroMatteo Alvaro
Matteo Alvaro
MMM.L. Mazzucchelli
M.L. Mazzucchelli
RAR.J. Angel
R.J. Angel
MMM. Murri
M. Murri
NCN. Campomenosi
N. Campomenosi
MMMarta Morana
Marta Morana
Metamorphic rocks are the records of plate tectonic processes whose reconstruction relies on correct estimates of the pressures and temperatures (P-T) experienced by these rocks through time. Unlike chemical geothermobarometry, elastic geobarometry does not rely on chemical equilibrium between minerals, so it has the potential to provide information on overstepping of reaction boundaries and to identify other examples of non-equilibrium behavior in rocks. Here we introduce a method that exploits the anisotropy in elastic properties of minerals to determine the unique P and T of entrapment from a single inclusion in a mineral host. We apply it to preserved quartz inclusions in garnet from eclogite xenoliths hosted in Yakutian kimberlites (Russia). Our results demonstrate that quartz trapped in garnet can be preserved when the rock reaches the stability field of coesite (the high-pressure and high-temperature polymorph of quartz) at 3 GPa and 850 °C. This supports a metamorphic origin for these xenoliths and sheds light on the mechanisms of craton accretion from a subducted crustal protolith. Furthermore, we show that interpreting P and T conditions reached by a rock from the simple phase identification of key inclusion minerals can be misleading.