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F.T. Manheim

Publications and source records attributed to F.T. Manheim.

At least 37 records · Page 2Linked to original sources
USGS1984

Ferromanganese micronodules from the surficial sediments of Georges Bank

Ferromanganese micronodules have been found on Georges Bank, off the U.S. northeast coast, distributed throughout the surficial sediments within an area about 125 km long and at least 12 km wide. These coarse, sand-sized concretions have precipitated from metal-rich interstitial waters and contain many of the textural and structural features common to other neritic nodules. Most of the nodules have accreted around detrital grains, and X-ray powder diffraction analyses indicate the presence of geothite and vernadite (  -MnO 2 ) in the ferromanganese layers. Chemical analyses of the micronodules, when compared with similar data on deep-sea manganese nodules, reveal lower Mn/Fe ratios, significantly higher concentrations of V and As, comparable values of Mo, and an order of magnitude less of Co, Ni, Ce and most other metals.

Georges Bank↗
USGS1984

Seismic reflection studies of sinkholes and limestone dissolution features on the northeastern Florida shelf

High-resolution seismic-reflection profiles show that the shelf off northern Florida is underlain by solution deformed limestone of Oligocene, Eocene, Paleocene and late Cretaceous age. Dissolution and collapse features are widely scattered. They are expressed in three general forms: as sinkholes that presently breach the sea floor, such as Red Snapper Sink and the Crescent Beach submarine spring; as sinkholes that have breached the seafloor in the past but are now filled with shelf sands; and as dissolution collapse structures that originate deep within the section and have caused buckling and folding of overlying Eocene, Oligocene, and to a lesser extent, Neogene strata. Although deformation caused by solution and collapse can be shown to be a continuous process, the major episode of karstification occurred in the late Oligocene and early Miocene when the shelf was exposed to subaerial conditions.

Conference Paper↗
USGS1982

Analysis of barium and strontium in sediments by dc plasma emission spectrometry

The dc plasma arc is suited to analysis of barium and strontium in a wide range of sedimentary rock matrices, from sands, shales, and carbonates, to ferromanganese nodules. Samples containing 10 ppm to more than 3000 ppm barium and strontium were studied. Both alkali (3500 ppm lithium borate, from a preliminary fusion) and lanthanum salts (1%) in the final solution are needed to achieve freedom from systematic effects due to extreme variation in matrix. In the absence of La, neither Li, Na, K, nor Cs totally eliminated effects of Al and other constituents on emission. Silica addition to the fusion helps achieve proper flux viscosity to aid removal of fused beads from graphite crucibles. The effect of refractory-substance formers such as aluminum with calcium can be reduced or removed by selection of a portion of the arc for emission measurement. However, it was decided not to pursue this approach because of loss in analytical sensitivity and need for greater precision in optical adjustment. Analysis of standard rock samples showed generally satisfactory agreement with precision methods of analysis, and some new standard rock data are reported.

Applied Spectroscopy↗
USGS1981

Patterns of groundwater salinity changes in a deep continental-oceanic transect off the southeastern Atlantic coast of the U.S.A.

Investigations of formation-fluid salinities in a transect from western Georgia to the edge of the Blake Plateau off the coast of Georgia show surprisingly similar hydrochemical features offshore and onshore. A fresh-brackish wedge of groundwater (<25 g/kg total dissolved solids) lies beneath the shelf to a depth of ∼ 900 m. On land, brackish waters extend to a maximum depth of ∼ 1.2 km below sea level in Lowndes County, Georgia. In deeper horizons, hypersaline brines (> 100 g/kg) occur in Lower Cretaceous (?) strata. These strata have a pronounced evaporitic (anhydritic) character in the offshore segment. Strong salinity gradients in interstitial waters signify buried evaporite deposits at drill sites beneath the Blake Plateau.

Florida, Georgia, South Carolina↗
USGS1979

U.S. Geological Survey core drilling on the Atlantic shelf

The first broad program of scientific shallow drilling on the U.S. Atlantic continental shelf has delineated rocks of Pleistocene to Late Cretaceous age, including phosphoritic Miocene strata, widespread Eocene carbonate deposits that serve as reflective seismic markers, and several regional unconformities. Two sites, off Maryland and New Jersey, showed light hydrocarbon gases having affinity to mature petroleum. Pore fluid studies showed that relatively fresh to brackish water occurs beneath much of the Atlantic continental shelf, whereas increases in salinity off Georgia and beneath the Florida-Hatteras slope suggest buried evaporitic strata. The sediment cores showed engineering properties that range from good foundation strength to a potential for severe loss of strength through interaction between sediments and man-made structures.

Science↗
USGS1976

Preliminary summary of the 1976 Atlantic Margin Coring Project of the U.S. Geological Survey

The U.S. Geological Survey Atlantic Margin Coring Project, 1976, a 60-day expedition to obtain core samples by drilling beneath the floor of the Continental Shelf and Slope of the eastern United States, was carried out in July, August, and September 1976 aboard D/V GLOMAR CONCEPTION. The coring penetrated as much as 310 meters below the sea floor at 19 sites along the continental margin from Georgia to Georges Bank off New England in water depths ranging from 20 to 300 meters; 1,020 meters of material were recovered in 380 cores, ranging in age from Late Cretaceous to Holocene. One of the major findings was the discovery of relatively fresh water (salinities less than 3 parts per thousand) extending beneath the Continental Shelf as much as 60 nautical miles seaward from the New Jersey coast. Water of about 1 part per thousand salinity was found beneath the shelf more than 7 nautical miles off Ocean City, Maryland and Barnegat Inlet, New Jersey. Analyses for light hydrocarbons in the cores show the highest concentrations (as much as 412,000 ppm) at sites in water depth greater than 200 meters (the shelf-slope break), principally in Pleistocene sediments, although methane concentrations greater than 400,000 ppm also were found in Miocene sediments at one site near the shelf edge. (Woodard-USGS)

Open-File Report↗
USGS1975

Interstitial solutions and diagenesis in deeply buried marine sediments: Results from the Deep Sea Drilling Project

Through the Deep Sea Drilling Project samples of interstitial solutions of deeply buried marine sediments throughout the World Ocean have been obtained and analyzed. The studies have shown that in all but the most slowly deposited sediments pore fluids exhibit changes in composition upon burial. These changes can be grouped into a few consistent patterns that facilitate identification of the diagenetic reactions occurring in the sediments. Pelagic clays and slowly deposited (<1 cm/10 3 yr) biogenic sediments are the only types that exhibit little evidence of reaction in the pore waters. In most biogenic sediments sea water undergoes considerable alteration. In sediments deposited at rates up to a few cm/10 3 yr the changes chiefly involve gains of Ca 2+ and Sr 2+ and losses of Mg 2+ which balance the Ca 2+ enrichment. The Ca-Mg substitution may often reach 30 mM/kg while Sr 2+ may be enriched 15-fold over sea water. These changes reflect recrystallization of biogenic calcite and the substitution of Mg 2+ for Ca 2+ during this reaction. The Ca-Mg-carbonate formed is most likely a dolomitic phase. A related but more complex pattern is found in carbonate sediments deposited at somewhat greater rates. Ca 2+ and Sr 2+ enrichment is again characteristic, but Mg 2+ losses exceed Ca 2+ gains with the excess being balanced by SO 4 post staggered2- losses. The data indicate that the reactions are similar to those noted above, except that the Ca 2+ released is not kept in solution but is precipitated by the HCO 3 post staggered- produced in SO 4 post staggered2- reduction. In both these types of pore waters Na + is usually conservative, but K + depletions are frequent. In several partly consolidated sediment sections approaching igneous basement contact, very marked interstitial calcium enrichment has been found (to 5.5 g/kg). These phenomena are marked by pronounced depletion in Na + , Si and CO 2 , and slight enhancement in Cl - . The changes are attributed to exchange of Na + for Ca 2+ in silicate minerals forming from submarine weathering of igneous rocks such as basalts. Water is also consumed in these reactions, accounting for minor increases in total interstitial salinity. Terrigenous, organic-rich sediments deposited rapidly along continental margins also exhibit significant evidences of alteration. Microbial reactions involving organic matter lead to complete removal of SO 4 post staggered2- , strong HCO 3 post staggered- enrichment, formation of NH 4 post staggered+ , and methane synthesis from H 2 and CO 2 once SO 4 post staggered2- is eliminated. K + and often Na + (slightly) are depleted in the interstitial waters. Ca 2+ depletion may occur owing to precipitation of CaCO 3 . In most cases interstitial Cl - remains relatively constant, but increases are noted over evaporitic strata, and decreases in interstitial Cl - are observed in some sediments adjacent to continents.

Geochimica et Cosmochimica Acta↗
USGS1973

Interstitial water studies on small core samples from the Mediterranean Sea

Of ten Leg 13 sites studied by us, eight give definite evidence of the existence of halite-containing sediments beneath the seabed. This conclusion is based on the existence on continuous sodium and chloride enrichments in interstitial waters with depth. This is the only direct evidence of the existence of salt at these sites, for only evaporitic dolomite, gypsum, and/or anydrite were recovered in cores. Among other ionic relationships, influence of evaporites is seen in calcium, magnesium and sulfate concentrations. Record high barium (216 ppm) and strontium (345 ppm) concentrations were observed in sulfate depleted pore fluids of Site 128 in the Hellenic Trench.

Initial reports of the Deep Sea Drilling Project↗
USGS1972

Interstitial water studies on small core samples, Leg 9

The chemistry of the pore fluids obtained on Leg 9 is remarkable primarily in its constancy. Excepting silicon and strontium, only at one site do the concentrations of the major and minor constituents deviate notably from sea water concentrations (see Tables 1 and 2). The trends, or lack of them, seen in these samples have been discussed previously and only references will be given here. The constancy of composition and similarity to sea water is particularly noteworthy, as the sediments at all of the 9 sites are thought to be intruded by the basal basalt. The pore fluid chemistry exhibits no evidence of intrusion except possibly at Site 84.

Initial reports of the Deep Sea Drilling Project↗
USGS1971

Interstitial water studies on small core samples, Deep Sea Drilling Project, Leg 6

Sediments from Leg 6 sites, west of the Hawaiian Islands, consisted primarily of various combinations of deep-sea biogenic oozes, volcanic ash, and its breakdown products. Pore fluids from most of the sites were similar in composition to present day ocean water, and in some sties almost identical. However, interstitial fluids from Site 53 (Philippine Sea) showed changes in ionic composition which were beyond those previously considered attributable to diagenetic influence. These samples show the beginnings of metamorphism by dramatic increases in calcium concentrations and corresponding decreases in alkali concentrations. Analytical methods were similar to those outlined in previous Leg Reports. However, obvious contamination of aliquots for sodium determination in the laboratory made it necessary to determine all sodium values by difference between anion and cation balances. These values are, if anything, more accurate than direct determinations which have been discussed in earlier legs. However, the authors will continue to analyze sodium directly, and in the future they may be able to improve the precision of the determinations to the point where small losses and gains of sodium in the pore fluids may be established accurately. Agreement between colorimetric and spectrometric determinations of silicon has improved, but there are still occasional marked differences for which the writers have no explanation. T. Takahashi has allowed the authors to compare total Carbon Dioxide (CO 2 ) measurements from his laboratory with their alkalinity determinations: both sets of data were obtained from fluids from the same squeezings of sediments and should give similar values at the indicated pH levels. Some disturbingly large discrepancies in the two sets of data are evident. The authors do not think that their back-titration alkalinity technique alone is responsible for the differences. However, they have not evaluated the possible influence of the heat-sealed polyethylene pipes on the alkalinity values; this should be considered a potential source of error. The pH data from water samples processed and measured on shipboard are reported here. In view of the major changes in pressure and temperature (laboratory temperatures were reported to be 26 to 28°C) and the sediments to new gaseous regimes prior to pH measurement, these values should be interpreted mainly as applying to the squeezed effluents, not to in situ values.

Initial reports of the Deep Sea Drilling Project↗
USGS1971

Interstitial water studies on small core samples, Deep Sea Drilling Project, Leg 8

Leg 8 sites are dominated by siliceous-calcareous biogenic oozes having depositional rates of 0.1 to 1.5 cm/1000 years. Conservative constituents of pore fluids showed, as have cores from other pelagic areas of the Pacific, insignificant or marginally significant changes with depth and location. However, in Sites 70 and 71, calcium, magnesium and strontium showed major shifts in concentration with depth. These changes appear to be related to recrystallization phenomena in skeletal debris of nannoplankton and to the relative accumulation rate of the sediments. The chemical anomalies increase relatively smoothly with depth, demonstrating the effectiveness of vertical diffusional communication, and apparent lack of bulk fluid movement, as noted in Leg 7 and other sites.

Initial reports of the Deep Sea Drilling Project↗
USGS1970

The diffusion of ions in unconsolidated sediments

Diffusion in unconsolidated sediments generally proceeds at rates ranging from half to one twentieth of those applying to diffusion of ions and molecules in free solution. Diffusion rates are predictable with respect to porosity and path tortuosity in host sediments, and can be conveniently measured by determinations of electrical resistivity on bulk sediment samples. Net ion flux is further influenced by reactions of diffusing species with enclosing sediments, but such influences should not be confused with or lumped with diffusion processes.

Earth and Planetary Science Letters↗
USGS1970

Suspended matter in surface waters of the Atlantic continental margin from Cape Cod to the Florida Keys

Appreciable amounts of suspended matter (> 1.0 milligram per liter) in surface waters are restricted to within a few kilometers of the Atlantic coast. Particles that escape estuaries or are discharged by rivers into the shelf region tend to travel longshoreward rather than seaward. Suspended matter farther offshore, chiefly amorphous organic particles, totals 0.1 milligram per liter or less. Soot, fly ash, processed cellulose, and other pollutants are widespread.

Atlantic Coast, Cape Cod to the Florida Keys↗
USGS1970

Brines and interstitial brackish water in drill cores from the deep Gulf of Mexico

Marked increases in interstitial salinity occur in two drill holes located in the Gulf of Mexico at a water depth of more than 3500 meters. The increases probably arose through diffusion of salt from buried evaporites. In one hole, however, brackish water was encountered on penetrating the oil-permeated cap rock of a salt dome. The phenomenon is attributed to production of fresh water during oxidation of petroleum hydrocarbons and decomposition of gypsum to form native sulfur.

Science↗
USGS1970

Interstitial water studies on small core samples, Deep Sea Drilling Project, Leg 3

Eleven samples of fluids which had been squeezed on board ship, and four, packaged sediment samples were received in our laboratories. As in Leg 2, the volumes of fluid available were scanty and did not permit multiple determinations of constituents in many of the samples; in Hole 21 the fluid available sufficed only for refractometer readings (a few tenths of a milliliter). Therefore, analytical scatter is again responsible for partially obscuring variations (and constancy) in the conservative constituents such as sodium. However, on the whole the results confirm the features which appeared in Legs 1 and 2. Central oceanic sediments display a remarkable constancy in total salinity, chlorinity and sodium concentration to the greatest depths and ages yet penetrated in the project drillings. Variations attributable to postburial reactions do occur in the remaining major ions, but they usually show little systematic trend with depth--with the exception of potassium, which will be discussed later. Methods remain similar to those employed for Leg 2; the detailed techniques are now being prepared for submission, but a brief description may be obtained from the previous Leg reports (Manheim and Sayles, 1969; Chan and Manheim, 1970). Results from four unsqueezed samples are not complete and, therefore, do not appear here.

Initial reports of the Deep Sea Drilling Project↗
USGS1970

Interstitial water studies on small core samples, Deep Sea Drilling Project, Leg 5

Leg 5 samples fall into two categories with respect to interstitial water composition: 1) rapidly deposited terrigenous or appreciably terrigenous deposits, such as in Hole 35 (western Escanaba trough, off Cape Mendocino, California); and, 2) slowly deposited pelagic clays and biogenic muds and oozes. Interstitial waters in the former show modest to slight variations in chloride and sodium, but drastic changes in non-conservative ions such as magnesium and sulfate. The pelagic deposits show only relatively minor changes in both conservative and non-conservative pore fluid constituents. As was pointed out in earlier Leg Reports, it is believed that much of the variation in chloride in pore fluids within individual holes is attributable to the manipulation of samples on board ship and in the laboratory. On the other hand, the scatter in sodium is due in part to analytical error (on the order of 2 to 3 per cent, in terms of a standard deviation), and it probably accounts for most of the discrepancies in total anion and cation balance. All constituents reported here, with the exception of bulk water content, were analyzed on water samples which were sealed in plastic tubes aboard ship and were subsequently opened and divided into weighed aliquots in the laboratory. Analytical methods follow the atomic absorption, wet chemical and emission spectrochemical techniques briefly summarized in previous reports, e.g. Manheim et al., 1969, and Chan and Manheim, 1970. The authors acknowledge assistance from W. Sunda, D. Kerr, C. Lawson and H. Richards, and thank D. Spencer, P. Brewer and E. Degens for allowing the use of equipment and laboratory facilities.

Initial reports of the Deep Sea Drilling Project↗
USGS1969

Geochemistry of pore waters from Shell Oil Company drill holes on the continental slope of the northern Gulf of Mexico

Pore waters were analyzed from 6 holes drilled from M.V. “Eureka” as a part of the Shell Oil Co. deeper offshore study. The holes were drilled in water depths of 600–3,000 ft. (approximately 180–550 m) and penetrated up to 1,000 ft. (300 m) of Pliocene-Recent clayey sediments. Salt and anhydrite caprock was encountered in one diapiric structure on the continental slope. Samples from holes drilled near diapiric structures showed systematic increases of pore-water salinity with depth, suggestive of salt diffusion from underlying salt plugs. Anomalous concentrations of K and Br indicate that at least one plug contains late-stage evaporite minerals. Salinities approaching halite saturation were observed. Samples from holes away from diapiric structures showed little change in pore-water chemistry, except for loss of SO 4 and other variations attributable to early-stage diagenetic reactions with enclosing sediments. Thus, increased salt concentrations in even shallow sediments from this part of the Gulf appear to provide an indicator of salt masses at depth.

Chemical Geology↗