Methane and hydrogen in mid-ocean-ridge basalt glasses: analysis by vacuum crushing

1988 ◽  
Vol 25 (1) ◽  
pp. 38-48 ◽  
Author(s):  
J. A. Welhan

A comparative study of vacuum crushing methods for analyzing reactive gases in basaltic glasses shows that ball milling is an efficient means of releasing occluded gases but that blank production represents a potentially serious problem that must be accounted for when determining reactive-gas compositions. Production of H2 and CH4 in a stainless-steel ball mill in the absence of rock material increases with length of crushing time. However, test results presented here indicate that blank levels are reduced during the actual crushing process by the presence of rock powder, which may act as a cushion to reduce metal–metal contact. Crushing in copper tubes under a hydraulic press produces no blanks for these gases, but crushing efficiency and gas release are very low, and gas adsorption on rock powder becomes a significant problem. Experiments with methane adsorption on crushed basalt suggest that the loss of methane is a chemisorption process that is, for the most part, irreversible.Applying corrections for these effects, we find that H2/CH4 ratios (~3 – 30) in mid-ocean-ridge basalt glasses are similar to those seen in high-temperature mid-ocean-ridge hydrothermal fluids. These data, arguments based on the similarity of water/rock mass ratios calculated from basalt gas data, and the uniformity of methane/helium ratios in divers high-temperature mid-ocean-ridge hydrothermal fluids support the contention that dissolved CH4 and H2 in these fluids are predominantly derived from leaching of mid-ocean-ridge basalt.

1986 ◽  
Vol 79 (3-4) ◽  
pp. 397-411 ◽  
Author(s):  
David M. Christie ◽  
Ian S.E. Carmichael ◽  
Charles H. Langmuir

Nature ◽  
1983 ◽  
Vol 306 (5942) ◽  
pp. 431-436 ◽  
Author(s):  
K. P. Jochum ◽  
A. W. Hofmann ◽  
E. Ito ◽  
H. M. Seufert ◽  
W. M. White

2000 ◽  
Vol 1 (8) ◽  
pp. n/a-n/a ◽  
Author(s):  
B. Bourdon ◽  
S. J. Goldstein ◽  
D. Bourlès ◽  
M. T. Murrell ◽  
C. H. Langmuir

Nature ◽  
1980 ◽  
Vol 283 (5743) ◽  
pp. 149-153 ◽  
Author(s):  
R. S. Cohen ◽  
N. M. Evensen ◽  
P. J. Hamilton ◽  
R. K. O'Nions

2009 ◽  
Vol 10 (5) ◽  
pp. n/a-n/a ◽  
Author(s):  
Fabrice J. Fontaine ◽  
William S. D. Wilcock ◽  
Dionysis E. Foustoukos ◽  
David A. Butterfield

Elements ◽  
2020 ◽  
Vol 16 (6) ◽  
pp. 389-394
Author(s):  
Esther M. Schwarzenbach ◽  
Matthew Steele-MacInnis

Seawater interaction with the oceanic lithosphere crucially impacts on global geochemical cycles, controls ocean chemistry over geologic time, changes the petrophysical properties of the oceanic lithosphere, and regulates the global heat budget. Extensive seawater circulation is expressed near oceanic ridges by the venting of hydrothermal fluids through chimney structures. These vent fluids vary greatly in chemistry, from the metal-rich, acidic fluids that emanate from “black smokers” at temperatures up to 400 °C to the metal-poor, highly alkaline and reducing fluids that issue from the carbonate–brucite chimneys of ultramafic-hosted systems at temperatures below 110 °C. Mid-ocean ridge hydrothermal systems not only generate signifi-cant metal resources but also host unique life forms that may be similar to those of early Earth.


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