Teruyuki Maruoka

Dr. Teruyuki Maruoka


Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

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

Representative Publications

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1 August 2008 in Applied Geochemistry
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Journal Article
Closed access
ASAshraf Ali Seddique
Ashraf Ali Seddique
HMHarue Masuda
Harue Masuda
MMMuneki Mitamura
Muneki Mitamura
KSKeiji Shinoda
Keiji Shinoda
TYToshiro Yamanaka
Toshiro Yamanaka
DBDipak Kumar Biswas
Dipak Kumar Biswas

9 February 2015 in Scientific Reports
Verified
Journal Article
Open access
PDF file
TKTakanori Kagoshima
Takanori Kagoshima
YSYuji Sano
Yuji Sano
NTNaoto Takahata
Naoto Takahata
TMTeruyuki Maruoka
Teruyuki Maruoka
TFTobias P. Fischer
Tobias P. Fischer
KHKeiko Hattori
Keiko Hattori
Evaluation of volcanic and hydrothermal fluxes to the surface environments is important to elucidate the geochemical cycle of sulphur and the evolution of ocean chemistry. This paper presents S/3He ratios of vesicles in mid-ocean ridge (MOR) basalt glass together with the ratios of high-temperature hydrothermal fluids to calculate the sulphur flux of 100 Gmol/y at MOR. The S/3He ratios of high-temperature volcanic gases show sulphur flux of 720 Gmol/y at arc volcanoes (ARC) with a contribution from the mantle of 2.9%, which is calculated as 21 Gmol/y. The C/S flux ratio of 12 from the mantle at MOR and ARC is comparable to the C/S ratio in the surface inventory, which suggests that these elements in the surface environments originated from the upper mantle.

1 February 2013 in Science of The Total Environment
Verified
Journal Article
Closed access
TMTakuya Matsumoto
Takuya Matsumoto
TMTeruyuki Maruoka
Teruyuki Maruoka
GSGen Shimoda
Gen Shimoda
HOHajime Obata
Hajime Obata
HKHiroyuki Kagi
Hiroyuki Kagi
PAPradeep Aggarwal
Pradeep Aggarwal

1 January 2003 in Earth and Planetary Science Letters
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Journal Article
Closed access
TMTeruyuki Maruoka
Teruyuki Maruoka
CKC Koeberl
C Koeberl
PHP.J Hancox
P.J Hancox
WRW.U Reimold
W.U Reimold

1 August 2007 in American Mineralogist: Journal of Earth and Planetary Materials
Verified
Journal Article
Closed access
PDF file
TETakuya Echigo
Takuya Echigo
MKMitsuyoshi Kimata
Mitsuyoshi Kimata
TMTeruyuki Maruoka
Teruyuki Maruoka
Karpatite from the Picacho Peak Area, San Benito County, California, has been characterized as an exceptionally pure crystal of coronene (C24H12) by infrared absorption analysis, Raman scattering analysis, and differential thermal analysis. Furthermore, the crystal structure of karpatite was determined using a single-crystal X-ray diffraction method for the first time. The mineral crystallizes in the monoclinic system, space group P21/a, with unit-cell dimensions of a = 16.094(9), b = 4.690(3), c = 10.049(8) Å, β = 110.79(2)°, V = 709.9(8) Å3, and Z = 2. The structure was solved and finally refined to R1 = 3.44% and wR2 = 2.65%, respectively. The coronene molecules in the crystal structure of karpatite are all isolated and the intermolecular distances correspond to van der Waals interactions. The coronene molecules have the high degree of aromaticity and no overcrowded hydrogen atoms, both of which avoid a mixing of other polycyclic aromatic hydrocarbons (PAHs) in karpatite. The corrugated arrangement of coronene molecules constituting karpatite prevents intercalation reactions, accounting for the exceptional purity of this mineral. The isotopic composition of carbon was measured, using an elemental analyzer-isotopic ratio mass spectrometer (EA/IRMS). The present karpatite yielded a δ13C value of −22.39 ± 0.18‰ (vs. VPDB), which is similar to carbon isotopic compositions of sedimentary organic matter in the far-reaching tectonic regions. This organic matter might be converted to coronene molecules by hydrothermal fluids leading to formation of karpatite. Textural relationships indicate that after the strong concentration of coronene molecules in hydrothermal fluids, karpatite growth postdates both hydrothermal quartz precipitation, and subsequent cinnabar formation.