Geology topics
Publications and source records attributed to Robert E. Garrison.
Explore the source record for details and available documents.
Diatomaceous sediments and their diagenetic equivalents in the Monterey Formation record a variable history of upwelling along the California margin. Distrinctive dark opal-CT and quartz chertz found in distal basins of the Monterey Formation are the result of burial diagenesis of pure biosiliceous oozes (biosiliceous oozes without significant admixtures of clay) and are therefore evidence of intensified coastal upwelling during the early middle Miocene. Dating of six sections of the Monterey Formation, largely by diatom biostratigraphy, suggests that at the Point Reyes and Point Año Nuevo sections in north-central California, the age of the earliest chert intervals is between 13.8 and 15.0 Ma, and 14.3 and 14.8 Ma, respectively. In south-central California, ages from the Shell Beach, Mussel Rock, and Lions Head sections imply that the age of the base of the chert intervals is between 12.7 and 13.3 Ma. Both ages correlate to an early middle Miocene high latitude cooling step that resulted in more vigorous surface water circulation, upwelling of nutrient-rich waters, and increased biosiliceous sedimentation in the North Pacific. The north-south difference in age of the base of the chert interval probably reflects a progressive intensification of the California Current from 15.0 to 12.7 Ma. The age of the onset of biosiliceous sedimentation at DSDP sites of the northeastern Pacific is also generally younger at the more southern sites; however, these particular DSDP sites were located some distance from the centres of coastal upwelling and are not as reliable indicators of the intensification of upwelling along the California margin.
Two distinct hydrogeochemical regimes currently dominate the Peruvian continental margin. One, in shallower water (150-450 m) shelf to upper-slope regions, is characterized by interstitial waters with strong positive chloride gradients with depth. The maximum measured value of 1043 mM chloride at Site 680 at ITS corresponds to a degree of seawater evaporation of ~2 times. Major ion chemistry and strontioum isotopic composition of the interstitial waters suggest that a subsurface brine that has a marine origin and is of pre-early Miocene "age," profoundly influences the chemistry and diagenesis of this shelf environment. Site 684 at ~9°S must be closest to the source of this brine, which becomes diluted with seawater and/or interstitial water as it flows southward toward Site 686 at ~13°S (and probably beyond) at a rate of approximately 3 to 4 cm/yr, since early Miocene time. The other regime, in deep water (3000-5000 m) middle to lower-slope regions, is characterized by interstitial waters with steep negative and nonsteady-state chloride gradients with depth. The minimum measured value of 454 mM chloride, at Site 683 at ITS, corresponds to —20% dilution of seawater chloride The most probably sources of these low-chloride fluids are gas hydrate dissociation and mineral (particularly clay) dehydration reactions. Fluid advection is consistent with (1) the extent of dilution shown in the chloride profiles, (2) the striking nonsteady-state depth profiles of chlorides at Sites 683 and 688 and of 87Sr/86Sr ratios at Site 685, and (3) the temperatures resulting from an average geothermal gradient of 50°C/km and required for clay mineral dehydration reactions. Strontium isotope data reveal two separate fluid regimes in this slope region: a more northerly one at Sites 683 and 685 that is influenced by fluids with a radiogenic continental strontium signature, and a southerly one at Sites 682 and 688 that is influenced by fluids with a nonradiogenic oceanic signatures. Stratigraphically controlled fluid migration seems to prevail in this margin. Because of its special tectonic setting, Site 679 at ITS is geochemically distinct. The interstitial waters are characterized by seawater chloride concentrations to —200 mbsf and deeper by a significantly lower chloride concentration of about two-thirds of the value in seawater, suggesting mixing with a meteoric water source. Regardless of the hydrogeochemical regime, the chemistry and isotopic compositions of the interstitial waters at all sites are markedly modified by diagenesis, particularly by calcite and dolomite crystallization.