Abstract
Fourier-transform infrared (FTIR) spectroscopy is commonly used to measure volatile contents dissolved in glass inclusions in minerals. The standard method is to doubly polish the crystal to fully expose the inclusion to allow infrared light to pass through the inclusion only. Glass inclusions are often a few tens of micrometers thick, which can limit the usefulness of FTIR because of how fragile samples become when thinned enough to doubly expose inclusions. Here, we test whether unexposed inclusions can be feasibly analyzed by measuring the dissolved volatile contents of a population of rehomogenized quartz-hosted glass inclusions at variable exposure levels. We analyzed 118 unexposed inclusions in 46 crystals. Of those, we analyzed the 74 inclusions in 38 crystals that survived being singly exposed. Of those, only 24 inclusions in 18 crystals remained to be analyzed when doubly exposed. Measuring the path length of light through the inclusion is critical to FTIR analyses. That length can be measured directly for doubly exposed inclusions. For those inclusions we find that water contents vary from 1.6 to 2.6 wt%, averaging 2.2 ± 0.3 wt%. Path length is difficult to measure, however, in singly exposed or unexposed inclusions. Indeed, we find that path length is variably underestimated when measured using a well-calibrated optical method. Despite that difficulty, the average water contents for the populations at each exposure level are statistically the same. But, on an inclusion-by-inclusion basis volatile contents at various exposure levels are highly discrepant because the typically underestimated thicknesses for non-doubly exposed inclusions result in anomalously high volatile contents. One way to measure path length in those inclusions is to reorient the host crystal to align the path length horizontally so it can be measured with the eyepiece reticle. Often, however, that technique proves impractical because small samples are difficult to handle. When path length cannot be measured directly, we find that using the average of the dimensions of the inclusion orthogonal to the path length can be used as a proxy for path length. That proxy allows volatile contents in unexposed inclusions to be analyzed accurately, which significantly reduces difficulties of sample preparation and can dramatically increase the number of potential target inclusions.
© 2015 by Walter de Gruyter Berlin/Boston
Articles in the same Issue
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- Blue spinel crystals in the MgAl2O4-CoAl2O4 series: Part I. Flux growth and chemical characterization
- Blue spinel crystals in the MgAl2O4-CoAl2O4 series: Part II. Cation ordering over short-range and long-range scales
- CO2 solubility in primitive martian basalts similar to Yamato 980459, the effect of composition on CO2 solubility of basalts, and the evolution of the martian atmosphere
- New structural features of the high-pressure synthetic sheet-disilicate Phase-X, K(2–x)Mg2Si2O7Hx
- Crystal structure refinements of borate dimorphs inderite and kurnakovite using 11B and 25Mg nuclear magnetic resonance and DFT calculations
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- In situ dehydration behavior of zeolite-like cavansite: A single-crystal X-ray study
- LREE-redistribution among fluorapatite, monazite, and allanite at high pressures and temperatures
- A single-crystal neutron diffraction study of hambergite, Be2BO3(OH,F)
- Analyzing water contents in unexposed glass inclusions in quartz crystals
- The atomic structure of deuterated boyleite ZnSO4·4D2O, ilesite MnSO4·4D2O, and bianchite ZnSO4·6D2O
- Synthesis and crystal chemistry of Fe3+-bearing (Mg,Fe3+)(Si,Fe3+)O3 perovskite
- Mixed-layered structure formation during trans-vacant Al-rich illite partial dehydroxylation
- Structural regularities in 2M1 dioctahedral micas: The structure modeling approach
- Incorporation of Fe and Al in MgSiO3 perovskite: An investigation by 27Al and 29Si NMR spectroscopy
- In situ high-temperature Raman and FTIR spectroscopy of the phase transformation of lizardite
- Packing systematics and structural relationships of the new copper molybdate markascherite and related minerals
- On the origin of sellaite (MgF2)-rich deposits in Mg-poor environments
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- First-principles study of self-diffusion and viscous flow in diopside (CaMgSi2O6) liquid
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Articles in the same Issue
- Cation ordering over short-range and long-range scales in the MgAl2O4-CuAl2O4 series
- Blue spinel crystals in the MgAl2O4-CoAl2O4 series: Part I. Flux growth and chemical characterization
- Blue spinel crystals in the MgAl2O4-CoAl2O4 series: Part II. Cation ordering over short-range and long-range scales
- CO2 solubility in primitive martian basalts similar to Yamato 980459, the effect of composition on CO2 solubility of basalts, and the evolution of the martian atmosphere
- New structural features of the high-pressure synthetic sheet-disilicate Phase-X, K(2–x)Mg2Si2O7Hx
- Crystal structure refinements of borate dimorphs inderite and kurnakovite using 11B and 25Mg nuclear magnetic resonance and DFT calculations
- Hydrogen-bond system and dehydration behavior of the natural zeolite parthéite
- In situ dehydration behavior of zeolite-like cavansite: A single-crystal X-ray study
- LREE-redistribution among fluorapatite, monazite, and allanite at high pressures and temperatures
- A single-crystal neutron diffraction study of hambergite, Be2BO3(OH,F)
- Analyzing water contents in unexposed glass inclusions in quartz crystals
- The atomic structure of deuterated boyleite ZnSO4·4D2O, ilesite MnSO4·4D2O, and bianchite ZnSO4·6D2O
- Synthesis and crystal chemistry of Fe3+-bearing (Mg,Fe3+)(Si,Fe3+)O3 perovskite
- Mixed-layered structure formation during trans-vacant Al-rich illite partial dehydroxylation
- Structural regularities in 2M1 dioctahedral micas: The structure modeling approach
- Incorporation of Fe and Al in MgSiO3 perovskite: An investigation by 27Al and 29Si NMR spectroscopy
- In situ high-temperature Raman and FTIR spectroscopy of the phase transformation of lizardite
- Packing systematics and structural relationships of the new copper molybdate markascherite and related minerals
- On the origin of sellaite (MgF2)-rich deposits in Mg-poor environments
- Edgrewite Ca9(SiO4)4F2-hydroxyledgrewite Ca9(SiO4)4(OH)2, a new series of calcium humite-group minerals from altered xenoliths in the ignimbrite of Upper Chegem caldera, Northern Caucasus, Kabardino-Balkaria, Russia
- Whelanite, Cu2Ca6[Si6O17(OH)](CO3)(OH)3(H2O)2, an (old) new mineral from the Bawana mine, Milford, Utah
- 2M1-phlogopite from Black Hills (South Australia): The first case of configurational polytype in micas
- Oxy-chromium-dravite, NaCr3(Cr4Mg2)(Si6O18)(BO3)3(OH)3O, a new mineral species of the tourmaline supergroup
- First-principles study of self-diffusion and viscous flow in diopside (CaMgSi2O6) liquid
- Browneite, MnS, a new sphalerite-group mineral from the Zakłodzie meteorite
- Mineralogical variation of silica induced by Al and Na in hydrothermal solutions