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S.M. Savin

Publications and source records attributed to S.M. Savin.

3 recordsLinked to original sources

Geothermometry, geochronology, and mass transfer associated with hydrothermal alteration of a rhyolitic hyaloclastite from Ponza Island, Italy

A rhyolitic hyaloclastite from Ponza Island, Italy, was hydrothermally altered, producing four distinct alteration zones based on X-ray diffraction mineralogy and field textures: (1) nonpervasive argillic zone; (2) propylitic zone; (3) silicic zone; and (4) sericitic zone. The unaltered hyaloclastite is volcanic breccia with clasts of vesiculated obsidian in a matrix of predominantly pumice lapilli. Incomplete alteration of the hyaloclastite resulted in the nonpervasive argillic zone, characterized by smectite and disordered opal-CT. The other three zones exhibit more complete alteration of the hyaloclastite. The propylitic zone is characterized by mixed-layer illite-smectite (I-S) with 10 to 85% I, mordenite, opal-C, and authigenic K-feldspar (akspar). The silicic zone is characterized by I-S with ???90% I, pure illite, quartz, akspar, and occasional albite. The sericitic zone consists primarily of I-S with ???66% I, pure illite, quartz, and minor akspar and pyrite. K/Ar dates of I-S indicate hydrothermal alteration occurred at 3.38 ?? 0.08 Ma. Oxygen isotope compositions of I-S systematically decrease from zones 1 to 4. In the argillic zone, smectite has ??18 O values of 21.7 to 22.0??? and I-S from the propylitic, silicic, and sericitic zones ranges from 14.5 to 16.3???, 12.5 to 14.0???, and 8.6 to 11.9???, respectively. ??18 O values for quartz from the silicic and sericitic zones range from 12.6 to 15.9???. By use of isotope fractionation equations and data from authigenic quartz-hosted primary fluid inclusions, alteration temperatures ranged from 50 to 65 ??C for the argillic zone, 85 to 125 ??C for the propylitic zone, 110 to 210 ??C for the silicic zone, and 145 to 225 ??C for the sericitic zone. Fluid inclusion data and calculated ??18 O water values indicate that hydrothermal fluids were seawater dominated. Mass-transfer calculations indicate that hydrothermal alteration proceeded in a relatively open chemical system and alteration in the sericitic zone involved the most extensive loss of chemical species, especially Si. Systematic gains in Mg occur in all alteration zones as a result of I-S clay mineral formation, and systematic losses of Na, Ca, and K occur in most zones. With the exception of Ca, calculations of mass transfer associated with hydrothermal alteration on Ponza agree with chemical fluxes observed in laboratory experiments involving hydrothermal reactions of rhyolite and seawater. The anomalous Ca loss at Ponza may be due to hydrothermal formation of anhydrite and later low-temperature dissolution. On the basis of Mg enrichments derived from circulating seawater, we estimate the following minimum water/rock ratios: 9, 3, 6, and 9 for the argillic, propylitic, silicic, and sericitic zones, respectively. Hydrothermal fluid pH for the propylitic and silicic zones was neutral to slightly basic and relatively acidic for the sericitic zone as a result of condensation of carbonic and perhaps other acids. Copyright ?? 2003 Elsevier Science Ltd.

Geochimica et Cosmochimica Acta↗

Does ice drive early Maastrichtian eustasy?

A large (30–40 m), rapid (≪1 m.y.), earliest Maastrichtian sea-level drop inferred from New Jersey sequence stratigraphic records correlates with synchronous δ 18 O increases in deep-water benthic and low-latitude surface-dwelling planktonic foraminifera. The coincidence of these events argues for the development of a moderate-sized ice sheet during the early Maastrichtian.

Geology↗

Miocene benthic foraminiferal isotope records: A synthesis

18 O/ 16 0 and 13 C/ 12 C ratios of Miocene benthic foraminifera from a number of Atlantic, Pacific and Indian Ocean DSDP sites (71, 77B, 206, 208, 238, 279, 289, 296, 329, 357 and 366A) have been compiled. These provide a rather detailed history of Miocene deep water especially in the Pacific Ocean. Bottom-water temperatures rose during the early Miocene and then declined rapidly during the middle Miocene. This decline was accompanied by an increase in Antarctic glaciation. Late Miocene bottom temperatures and Antarctic ice volumes are inferred to be similar to today's, but exhibited some fluctuation. The early Miocene ocean was less thermally stratified at intermediate and abyssal depths while the late Miocene deep ocean had a thermal structure generally similar to the modern ocean. Foraminiferal carbon isotope ratios at most of the sites varied quasi-sympathetically throughout the Miocene. These variations must reflect comparable variations in the mean 13 C/ 12 C of marine HCO 3 . However, the causes of such variations are not yet clear.

Marine Micropaleontology↗