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J. N. Batchelder

Publications and source records attributed to J. N. Batchelder.

3 recordsLinked to original sources

Stable isotope and fluid inclusion studies of carbonate deposits from the Tolfa Mountains mining district (Latium, central Italy)

Carbon and oxygen isotope analyses were made of representative samples of calcite and quartz from the carbonate deposits in the Tolfa Mountains mining district. Measurements were also made of hydrogen isotope compositions, filling temperatures and salinities of fluid inclusions in these minerals. There are three stages of mineralization at Tolfa. In stage I, characterized by calc-silicate hornfels, the carbonates have relatively high ?? 18O values of 14.5 to 21.6 suggesting a rather low water/rock ratio. ??13C values of -0.3 to 2.1 indicate that appreciable decarbonation or introduction of deep-seated carbon did not occur. Stage II is marked by phanerocrystalline carbonates; ?? 18O values of 13.1 to 20.0 and ??13C values of 0.7 to 5.0 identify them as hydrothermal veins rather than marbles. ?? D values of -56 to -50 for inclusion fluids suggest a possible magmatic component to the hydrothermal fluid. Filling temperatures of coarse-grained samples of Calcite II are 309?? to 362?? C with a salinity range of 5.3 to 7.1 weight percent NaCl. Calculated ??18O values of 11-12 for these fluids are again indicative of low water/rock ratios. The sparry calcites of stage III have ??18O and ??13C values of 8.1 to 12.9 and -1.7 to 3.2, respectively. ?? D values of inclusion fluids are -40 to -33, clearly heavier than in earlier stages and similar to values of modern local ground waters. A salinity measurement of <0.1 weight percent NaCl in a sample of Calcite III is compatible with a relatively unaltered ground water origin for this fluid. Precipitation of the sparry calcite took place at much lower temperatures, around 160?? C. For quartz, ??18O values of 9.3 to 12.4 and ?? D values for inclusions of -53 to -28 are consistent with its late occurrence and paragenetic link with associated carbonates. ?? 1980 Springer-Verlag.

Mineralium Deposita

CO2-filled vesicles in mid-ocean basalt

Volatile-filled vesicles are present in minor amounts in all samples of mid-ocean basalt yet collected (and presumably erupted) down to depths of 4.8 km. When such vesicles are pierced in liquid under standard conditions, the volume expansion of the gas is 0.2 ?? 0.05 times the eruption pressure in bars or 20 ?? 5 times the eruption depth in km. Such expansion could be used as a measure of eruption depth. A variety of techniques: (1) vacuum crushing and gas chromatographic, freezing separation, and mass spectrographic analyses; (2) measurements of phase changes on a freezing microscope stage; (3) microscopic chemical and solubility observations; and (4) volume change measurements, all indicate that CO2 comprises more than 95% by volume of the vesicle gas in several submarine basalt samples from the Atlantic and Pacific. The CO2 held in vesicles is present in quantities about equal to or greater than that presumed to be dissolved in the glass (melt) and amounts to 400-900 ppm of the rock. The rigid temperature of the glass is 800-1000??C and increases for shallower samples. A sulfur gas was originally present in subordinate amounts in the vesicles, but has largely reacted with iron in the vesicle walls to produce sulfide spherules. ?? 1977.

Journal of Volcanology and Geothermal Research