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Interstitial water studies on small core samples, leg 19

The sediments cored on Leg 19 consist primarily of diatomaceous oozes with variable proportions of volcanic material and terrigenous clays and silts. With a few exceptions, deposition rates are high at these sites, usually exceeding 5cm/10 3 y. The interstitial solutions sampled exhibit compositional changes which previously have been found to characterize rapidly deposited terrigenous sediments. Some of the largest changes in Na + , K + , Mg 2+ , Cl - , and HCO 3 yet found in DSDP samples occur in the pore waters studied from this leg (see Table 1).

Initial reports of the Deep Sea Drilling Project

Interstitial water studies on small core samples, Leg 15

Analyses of pore fluids from reducing environments demonstrate that reduction of SO 4 is accompanied by large increases in alkalinity and strong depletion of Ca and Mg. The data are compatible with a model of replacement of Fe 3+ in clay lattices by Mg from the interstitial solutions and the precipitation of pyrite. Depletions of Na in the interstitial solutions are related to Mg losses by a ratio of approximately 1:3. Pore fluids from oxidizing pelagic sediments exhibit little SO 4 depletion. Losses of Mg are accompanied by the addition of Ca to the pore solutions on a nearly 1:1 basis. Strong Sr enrichment is also found in these solutions. The magnitude of the Sr increase suggests that considerable carbonate recrystallization has occurred. As part of an extensive interlaboratory and analytical calibration, the effect of squeezing sediment at different temperatures has been studied in depth. Samples of a variety of lithologies have been included. Enrichment of K by as much as 24 percent and depletion of Mg and Ca by up to 7 percent occurs during warming. However, no significant effect upon Cl and SO 4 could be detected. The strongest effects are seen in the minor constituents studied. On warming, Sr, Si, and B are enriched as much as 19, 40, and 60 percent, respectively. The size of the observed concentration changes varies with the mineralogy of the sediment, but is significant in all types studied, particularly with regards to Mg and K.

Initial reports of the Deep Sea Drilling Project

Interstitial water studies on small core samples, Leg 22

Interstitial waters from Leg 22 in the Indian Ocean revealed two unique results: Site 214, on the Ninetyeast Ridge, penetrated through a 30-meter sequence of fine-grained basalt and reentered hard, silty clay containing carbonate skeletal debris. Such a basalt layer may well have been impervious and extensive enough to seal off underlying (fossil) seawater of Paleocene age. However, except for a marked increase in calcium and a slight increase in chloride, no appreciable changes in pore fluid chemistry could be confirmed. Site 217, at the northernmost end of the Ninetyeast Ridge, demonstrated record concentrations of interstitial calcium in clayey nannofossil oozes and a relatively small but significant increment in chloride with depth. Presumably, these increments signal the existence of evaporitic sediments or evaporite-influenced brines at considerably greater depth than penetrated.

Initial reports of the Deep Sea Drilling Project

Diffusimetry (diffusion constant estimation) on sediment cores by resistivity probe

Measurement of formation factor (ratio of rock resistivity to interstitial water resistivity) from sediment cores provides an indirect measurment of the tortuosity of the fluid channels in the sediments. From these measurements one can estimate the diffusion coefficient of the sediment with depth. The F (formation factor) values for Indian Ocean sediments varied from 1.6 for a clayey diatom ooze having 87% porosity (70% water content) to 13.6 for a cemented limestone having 25% porosity (11% water content). These formation factors would yield diffusion coefficients for chloride ions in the corresponding sediments of 6.4 x 10 -6 to 1.5 x 10 -6 cm 2 /sec. In general, surficial sediments showed diffusion coefficients about one-half to one-third of those for free solution, values decreasing with depth and porosity.

Initial reports of the Deep Sea Drilling Project

Porosity, density, grain density, and related physical properties of sediments from the Red Sea drill cores

Representative sediments from each site were chosen for examination of their dry specific gravity and grain density. The determinations were made by micropycnometer; water was used as the displacing medium, and salt corrections were based on the refractive index measurements on interstitial water. For saltier brines the "salinities" derived from index of refraction are somewhat too low but, for the most part, are adequate for these corrections. Water contents are those determined on the archived samples selected for these studies. They had been kept in cold storage (4°C) in screw-capped glass bottles with poly seal lids or in heat-sealed polyethylene bags for a period of about three months. The purpose of the measurements was to gain sufficient information on grain density to permit application of the general information or pattern to the bulk water content determinations on the small syringe samples. Bulk density, porosity, and other properties could then be calculated without using volume measurements from the syringes. Whereas the data from weight loss on drying (bulk water content) at 110-120° were considered good, the volume measurements are subject to considerable error, especially in more consolidated sediments, and are not usable at all for shales, more consolidated or cemented rocks, and anhydrite. Detailed comparisons with the GRAPE determinations were also an objective. The Red Sea cores offer a particularly good opportunity to test the validity of these measurements, which have been increasingly questioned.

Initial reports of the Deep Sea Drilling Project

Chemical analyses of Red Sea sediments

One of the prime motives for exploring the deeper subsurface sediments of the Red Sea floor was to gain information on the geochemical systems controlling the hot brine-metalliferous deposits. Accordingly, a strong effort was made to provide both shipboard and laboratory means of analysis of the recovered phases. Shipboard spectrographic analyses (semiquantitative) provided both detailed surveys of chemical properties of the cores and the ability to analyze small subsamples and separated particles such as pyrite, sphalerite, organisms, and similar minute objects. Over 5000 such analyses are provided in Tables 1 to 5. Some supplementary data provided by subsequent analyses for K, Zn, and Ag in the Denver field laboratories of the U. S. Geological Survey have been added to the tables. A second body of data is provided in Table 6, which gives quantitative data on major and minor constituents, performed by the Washington analytical laboratories of the U. S. Geological Survey. A third group of analyses are partial analyses on evaporitic rocks (anhydrite and rock salt) (Table 18, in Manheim Chapter 38, this volume). In addition to the above, a number of the collaborating laboratories are providing more specific chemical data on special phases and constituents of the Red Sea materials. Most of these data are included in chapters in the Geochemical section of this volume. The significance of the data is discussed in Manheim (Chapter 38, this volume) and in the respective reports of shipboard workers and cooperating share laboratories.

Initial reports of the Deep Sea Drilling Project

Red Sea geochemistry

The Red Sea drillings reveal a number of new facets of the hot-brine-metalliferous system and other geochemical aspects of the sea, its sediments, and its past history as follows: 1) Dark shales rich in organic material, and containing enhanced Mo and V concentrations, are characteristic of Plio-Pleistocene strata in the Red Sea. Values as high as 1500 ppm V and 500 ppm Mo were obtained in sediments containing up to 8 percent organic carbon. 2) Metalliferous sediments in the hot brine deep (Site 226) are similar in composition in both solids and interstitial water to previously analyzed sediments. However, one site (228) well south of the known hot-brine deeps shows zinc mineralization reaching 5 percent Zn in late Miocene shale-anhydrite breccias. 3) Pore fluid studies show that near-saturated (NaCl) brines having similar total salt concentration to the hot-brine fluids are associated with Miocene evaporites at Sites 225, 227, and 228. However, their chemical and isotopic composition precludes such fluids being part of the "hot brine plumbing system." Hydrogen and oxygen isotope studies demonstrate that fluids trapped between and among the evaporitic rocks have a strong meteoric water component, presumed to have entered the rocks during or shortly after formation in shallow evaporating pans. The composition of pore fluid at Site 227 suggests the presence of late-stage evaporite minerals of the tachyhydrite CaMg 2 Cl 6 • 12H 2 O series in the in situ rocks. 4) Diffusivity measurements show that the pre-Miocene strata permit dissolved salt or gas diffusion to the extent of from 1/2 to about 1/10 the rate in free solution. However, in anhydrites diffusivity is reduced more than 100-fold, and no diffusion could be detected through halite rock. The rates applied to interstitial salt gradients at Site 225 suggest that less than 1 meter of rock salt is removed per million years by diffusion processes. The diffusion of salt can already be detected a few meters below the sediment-water interface, and based on the interstitial water studies, one can affirm the presence of salt at depth at Sites 228, 230, and possibly 229, where rock salt was not encountered by the drill. 5) Isotopic measurements on leads show that both leads from Site 228 and the hot brine deep (Site 226) require input from igneous or volcanic sources (e.g., volcanic ash). Elsewhere, however, leads of sedimentary-pelagic origin are noted. 6) Isotopic and other evidence indicates that the long-distance transport of subterranean brines advocated by Craig (1969) is unlikely. Instead, it is proposed that the source of the hot brines is subevaporite clastic or other aquifers of early to middle Miocene age that have been disrupted by rifting. These discharge in the deeps by virtue of hydrodynamic continuity with heavy brines at higher positions on the nearby flanks of the Red Sea. In this case, the waters might be fossil (middle Miocene) Red Sea waters of relatively normal salinity that have acquired greater salt concentration by diffusion from overlying late Miocene evaporites. The model is consistent with the isolated nature of the brine deeps and suggests that flow might have been enhanced by increased hydraulic gradients during periods of lowered Red Sea levels. 7) Interstitial water evidence indicates that Pleistocene lowerings of sea level did not cause evaporative conditions leading to actual gypsum or other evaporite deposition in the deeper water zones, as has been postulated. This in turn suggests that sill depths were greater than have been assumed.

Initial reports of the Deep Sea Drilling Project

Natural remanent magnetization, mag¬netic properties, and oxidation of titanomagnetite in basaltic rocks from DSDP Leg 34

We have made paleomagnetic measurements and investigated the magnetic mineralogy of 24 samples of basalt and diabase from Sites 319, 320, and 321 on the Nazca plate. Sample distributions, locations, and ages of overlying sediments are as follows: Site 319, Hole 319, lat 13°01.04'S, long 101°31.46'W, 2 samples, early Miocene (N8); Site 319, Hole 319A, (same coordinates and age), 12 samples. Site 320, Hole 320B, lat 9°00.40'S, long 83°31.8O'W, 2 samples, late Oligocene (N2); Site 321, lat 12°01.29'S, long 81°54.24'W, 8 samples, late Eocene (P16). The objectives were (1) to investigate the stability of the natural remanent magnetization (NRM), (2) to evaluate an improved method of alternating-field (AF) demagnetization, (3) to determine the directions of the magnetically stable components of NRM and the approximate in-situ intensities of NRM, (4) to identify the ferrimagnetic minerals and determine their degree of oxidation, and (5) to relate this oxidation to the magnetic characteristics of the minerals.

Initial reports of the Deep Sea Drilling Project

Interstitial water studies on small core samples, leg 4

Reorganization and recodification of shipboard procedures for collecting interstitial waters has resulted in improved and more regular collection and analysis of pore fluids. Comparative studies of waters squeezed and analyzed on shipboard and analyzed in the shore laboratory show generally good agreement, except for some aberrations whose sources are hard to track down. Influences of pressure and temperature during squeezing on composition of effluents were re-examined for clayey samples from Leg 4 cores. Pressure was not found to be significant, whereas the temperature effects are significant, but are less than variations attributable to diagenetic reactions in the sediments. Conservative constituents, such as, chloride, sodium and bromide, remain relatively constant (within about 1.5 per cent) with changing depth in the holes; but, large depletions with respect to normal sea water occur in calcium (to 0.06 g/kg), magnesium (to 0.7), potassium (to 0.20), and sulfate (to 0.11) in most of the cores. On the other hand, large enrichments of calcium (to 1.57 g/kg) and lithium (to 1.7 ppm) occurred in Holes 24 and 24A. The depletion of several constituents in pore waters of Hole 26 (Vema fracture zone) caused a drop in total salt content to as low as 31 o/oo. However, no real dilution effects are involved, since chloride and sodium values remain typical of those in ocean bottom waters.

Initial reports of the Deep Sea Drilling Project

Petrographic and chemical characteristics of pyrite-marcasite mineralization in hole 465A, southern Hess Rise

Core recovered from Hess Rise contains concentrations of pyrite, marcasite, and barite in the lowermost meter of limestone (Unit II) and in the brecciated upper part of the underlying volcanic basement (Unit HI). Petrographic and chemical data indicate that the sulfide-barite assemblage in the limestone is mainly a product of low-temperature diagenetic processes. The iron-sulfide phases are biogenic and their concentrations mark the diffusion of sea water sulfate through sedimentary horizons containing abundant organic matter and mafic, glassy volcanogenic detritus. There is some evidence, however, that elevated temperatures augmented or intensified the synsedimentary diagenetic process.

Initial reports of the Deep Sea Drilling Project

Site 548

No abstract available.

Initial reports of the Deep Sea Drilling Project

Site 549

No abstract available.

Initial reports of the Deep Sea Drilling Project

Site 550

No abstract available.

Initial reports of the Deep Sea Drilling Project

Site 551

No abstract available.

Initial reports of the Deep Sea Drilling Project