Andrew Menzies

Dr. Andrew Menzies

Bruker Nano Analytics GmbH, 12489 Berlin, Germany

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

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

Representative Publications

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1 September 2004 in Lithos
Verified
Journal Article
Closed access
HGHerman S. Grütter
Herman S. Grütter
JGJohn J. Gurney
John J. Gurney
AMAndrew Menzies
Andrew Menzies
FWFerdi Winter
Ferdi Winter

4 January 2006 in Journal of Petrology
Verified
Journal Article
Open access
PDF file
HGHerman Grütter
Herman Grütter
DLDewetia Latti
Dewetia Latti
AMAndrew Menzies
Andrew Menzies
The spinel–garnet transition in Cr/Al-enriched peridotitic bulk compositions is known from experimental investigations to occur at 20–70 kbar, within the pressure range sampled by kimberlites. We show that the Cr2O3–CaO compositions of concentrate garnets from kimberlite have maximum Cr/Ca arrays characterized by Cr2O3/CaO ∼0·96–0·81, and interpret the arrays as primary evidence of chromite–garnet coexistence in Cr-rich harzburgitic or lherzolitic bulk compositions derived from depth within the lithosphere. Under Cr-saturated conditions on a known geotherm, each Cr/Ca array implicitly delineates an isobar inside a garnet Cr2O3–CaO diagram. This simplification invites a graphical approach to calibrate an empirical Cr/Ca-in-pyrope barometer. Carbonaceous chromite–garnet harzburgite xenoliths from the Roberts Victor kimberlite tightly bracket a graphite–diamond constraint (GDC) located at Cr2O3 = 0·94CaO + 5·0 (wt %), representing a pivotal calibration corresponding to 43 kbar on a 38 mW/m2 conductive geotherm. Additional calibration points are established at 14, 17·4 and 59·1 kbar by judiciously projecting garnet compositions from simple-system experiments onto the same geotherm. The garnet Cr/Ca barometer is then simply formulated as follows (in wt %): A small correction to P38 values, applicable for 35–48 mW/m2 conductive geotherms, is derived empirically by requiring conventional thermobarometry results and garnet concentrate compositions to be consistent with the presence of diamonds in the Kyle Lake kimberlite and their absence in the Zero kimberlite. We discuss application of the P38 barometer to estimate (1) real pressures in the special case where chromite–garnet coexistence is known, (2) minimum pressures in the general case where Cr saturation is unknown, and (3) the maximum depth of depleted lithospheres, particularly those underlying Archaean cratons. A comparison with the PCr barometer of Ryan et al. (1996, Journal of Geophysical Research 101, 5611–5625) shows agreement with P38 at 55 ± 2 kbar, and 6–12% higher PCr values at lower P38. Because the PCr formulation systematically overestimates the 43 kbar value of the GDC by 2–6 kbar, we conclude that the empirical Cr/Ca-in-garnet barometer is preferred for all situations where conductive geotherms intersect the graphite–diamond equilibrium.

1 July 2001 in Geophysical Research Letters
Verified
Journal Article
Closed access
PDF file
SSSteven B. Shirey
Steven B. Shirey
RCRichard W. Carlson
Richard W. Carlson
SRStephen H. Richardson
Stephen H. Richardson
AMAndrew Menzies
Andrew Menzies
JGJohn J. Gurney
John J. Gurney
UWUwe Wiechert
Uwe Wiechert

1 September 2004 in Lithos
Verified
Journal Article
Closed access
AMAndrew Menzies
Andrew Menzies
KWKalle Westerlund
Kalle Westerlund
HGHerman Grütter
Herman Grütter
JGJohn Gurney
John Gurney
JCJon Carlson
Jon Carlson
TNTom Nowicki
Tom Nowicki

23 June 2016 in Contributions to Mineralogy and Petrology
Verified
Journal Article
Closed access
PDF file
YBYannick Bussweiler
Yannick Bussweiler
RSR. S. Stone
R. S. Stone
DPD. G. Pearson
D. G. Pearson
RLR. W. Luth
R. W. Luth
TST. Stachel
T. Stachel
AMAndrew Menzies
Andrew Menzies

14 February 2018 in Antonie van Leeuwenhoek
Verified
Journal Article
Closed access
PDF file
JTJ. Tapia
J. Tapia
RTRodrigo Gonzalez T.
Rodrigo Gonzalez T.
BTB. Townley
B. Townley
VOV. Oliveros
V. Oliveros
FAFernanda Alvarez-Amado
Fernanda Alvarez-Amado
MCM. Calderón
M. Calderón