Frank T. Manheim
United States Geological Survey
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Featured researches published by Frank T. Manheim.
Geochimica et Cosmochimica Acta | 1966
A.R Miller; C.D Densmore; E.T Degens; J.C Hathaway; Frank T. Manheim; P.F McFarlin; R Pocklington; A Jokela
Abstract Sedimentary iron and heavy-metal deposits of undetermined size have been found in the middle of the Red Sea some 2000 meters below the surface of the sea (Fig. 1). This discovery has been made from the Research Vessel Atlantis II, which is still at sea engaged in a series of oceanographic investigations which ultimately will end in November 1965, after the ship has circumnavigated the globe. The discovery is significant because the environment and the processes controlling deposition of heavy metals are observable and appear to be still active.
Science | 1979
John C. Hathaway; C. Wylie Poag; Page C. Valentine; Frank T. Manheim; Francis A. Kohout; Michael H. Bothner; Robert E. Miller; David M. Schultz; Dwight A. Sangrey
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 Georgla 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.
Earth and Planetary Science Letters | 1970
Frank T. Manheim
Abstract 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.
Geochimica et Cosmochimica Acta | 1961
Frank T. Manheim
Abstract An investigation has been made of the relationship between depositional environment and element distribution in sediments from the Baltic Sea. A prominent feature of the Baltic is its salinity stratification, which gives rise to changes in bottom character from oxygenation to stagnation as greater depths are approached. Maximum heavy metal concentrations were not found in the contral, most stagnant and organic-rich parts of the basins, but in the transition zone to stagnant conditions. Manganese-iron nodules were found in a peripheral area characterized by aerated bottom water but moderately reducing sediment environment, as measured by redox potential determinations. In two of the Baltic deeps manganese was found enriched in sapropelic sediments, in one case reaching 5.2 per cent MnO. The mineral responsible for the enrichment is regarded as a mixed manganese-calcium carbonate.
Geological Society, London, Special Publications | 1997
James R. Hein; Andrea Koschinsky; Peter Halbach; Frank T. Manheim; Michael Bau; Jung-Keuk Kang; Naomi Lubick
Abstract Iron, manganese, and iron-manganese deposits occur in nearly all geomorphologic and tectonic environments in the ocean basins and form by one or more of four processes: (1) hydrogenetic precipitation from cold ambient seawater, (2) precipitation from hydrothermal fluids, (3) precipitation from sediment pore waters that have been modified from bottom water compositions by diagenetic reactions in the sediment column and (4) replacement of rocks and sediment. Iron and manganese deposits occur in five forms: nodules, crusts, cements, mounds and sediment-hosted stratabound layers. Seafloor oxides show a wide range of compositions from nearly pure iron to nearly pure manganese end members. Fe/Mn ratios vary from about 24 000 (up to 58% elemental Fe) for hydrothermal seamount ironstones to about 0.001 (up to 52% Mn) for hydrothermal stratabound manganese oxides from active volcanic arcs. Hydrogenetic Fe-Mn crusts that occur on most seamounts in the ocean basins have a mean Fe/Mn ratio of 0.7 for open-ocean seamount crusts and 1.2 for continental margin seamount crusts. Fe-Mn nodules of potential economic interest from the Clarion-Clipperton Zone have a mean Fe/Mn ratio of 0.3, whereas the mean ratio for nodules from elsewhere in the Pacific is about 0.7. Crusts are enriched in Co, Ni and Pt and nodules in Cu and Ni, and both have significant concentrations of Pb, Zn, Ba, Mo, V and other elements. In contrast, hydrothermal deposits commonly contain only minor trace metal contents, although there are many exceptions, for example, with Ni contents up to 0.66%, Cr to 1.2%, and Zn to 1.4%. Chondrite-normalized REE patterns generally show a positive Ce anomaly and abundant ΣREEs for hydrogenetic and mixed hydrogenetic-diagenetic deposits, whereas the Ce anomaly is negative for hydrothermal deposits and ΣREE contents are low. However, the Ce anomaly in crusts may vary from strongly positive in East Pacific crusts to slightly negative in West Pacific crusts, which may reflect the redox conditions of seawater. The concentration of elements in hydrogenetic Fe-Mn crusts depends on a wide variety of water column and crust surface characteristics, whereas concentration of elements in hydrothermal oxide deposits depends of the intensity of leaching, rock types leached, and precipitation of sulphides at depth in the hydrothermal system.
Geochimica et Cosmochimica Acta | 1975
Frederick L. Sayles; Frank T. Manheim
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/103yr) 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/103 yr the changes chiefly involve gains of Ca2+ and Sr2+ and losses of Mg2+ which balance the Ca2+ enrichment. The Ca-Mg substitution may often reach 30 mM/kg while Sr2+ may be enriched 15-fold over sea water. These changes reflect recrystallization of biogenic calcite and the substitution of Mg2+ for Ca2+ 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. Ca2+ and Sr2+ enrichment is again characteristic, but Mg2+ losses exceed Ca2+ gains with the excess being balanced by SO4post staggered2− losses. The data indicate that the reactions are similar to those noted above, except that the Ca2+ released is not kept in solution but is precipitated by the HCO3post staggered− produced in SO4post 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 CO2, and slight enhancement in Cl−. The changes are attributed to exchange of Na+ for Ca2+ 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 SO4post staggered2−, strong HCO3post staggered− enrichment, formation of NH4post staggered+, and methane synthesis from H2 and CO2 once SO4post staggered2− is eliminated. K+ and often Na+ (slightly) are depleted in the interstitial waters. Ca2+ depletion may occur owing to precipitation of CaCO3. 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.
Science | 1986
Frank T. Manheim
Ferromanganese oxides in the open oceans are more enriched in cobalt than any other widely distributed sediments or rocks. Concentrations of cobalt exceed 1 percent in ferromanganese crusts on seamounts, ocean ridges, and other raised areas of the ocean. The cobaltrich crusts may be the slowest growing of any earth material, accumulating one molecular layer every 1 to 3 months. Attention has been drawn to crusts as potential resources because they contain cobalt, manganese, and platinum, three of the four priority strategic metals for the United States. Moreover, unlike abyssal nodules, whose recovery is complicated by their dominant location in international waters, some of the most cobalt-rich crusts occur within the exclusive economic zone of the United States and other nations. Environmental impact statements for crust exploitation are under current development by the Department of the Interior.
Journal of Sedimentary Research | 1980
Donald W. Eggimann; Frank T. Manheim; Peter R. Betzer
ABSTRACT The analytical estimation of amorphous silica in selected Atlantic and Antarctic Ocean sediments, the U.S.G.S. standard marine mud (MAG-1), A.A.P.G. clays, and samples from cultures of a marine diatom, Hemidiscus, has been examined. Quantitative recovery of sedimentary amorphous silica was achieved by reacting 2 M Na2CO3 with a sample for 4 hours at 90°-100° C; where necessary, aluminum analysis is used to correct for the extraction of non-amorphous silica. Oceanic sediments having an amorphous SiO2/clay ratio of 1.0 or more can be analyzed by a single extraction with 2 M Na2CO3, without correction for non-amorphous additions. Marine sediments having an amorphous SiO2/clay ratio of from 1.0 to 0.25 can be corrected for inputs of clay-derived silica using an aluminum determination and an empirical correction factor. Sediments with amorphous SiO2/clay ratios of less than 0.25, samples containing non-silica-bearing aluminous materials such as gibbsite, or materials having low absolute levels of amorphous silica require successive leaches to accurately correct for silica inputs from non-amorphous sources. Our values for amorphous silica-rich circum-Antarctic sediments are equal to or greater than literature values, whereas our values for a set of amorphous silica-poor sediments from a transect of the North Atlantic at 11°N, after appropriate correction for silica released from clays, are significantly lower than previous estimates from the same region.
Science | 1970
Frank T. Manheim; Robert H. Meade; Gerard C. Bond
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.
Marine Geology | 1985
James R. Hein; Frank T. Manheim; William C. Schwab; Alicé S. Davis
Abstract Necker Ridge, Horizon Guyot and S.P. Lee Guyot in the Central Pacific were sampled, seismically surveyed, and photographed by bottom cameras in order to better understand the distribution, origin, and evolution of ferromanganese crusts. Necker Ridge is over 600 km long with a rugged crest, pods of sediment to 146 m thick, slopes that average 12° to 20°, and debris aprons that cover some of the lower flanks. Substrate lithologies are mostly hyaloclastite, volcaniclastic breccia, and minor alkalic basalt. Horizon Guyot, 300 km long and 75 km wide, is capped by at least 160 m of sediment, which buries stepped terraces. Substrate lithologies are similar to those on Necker Ridge, although previous workers sampled much tholeiitic basalt on Horizon. S.P. Lee Guyot, 125 km long and 80 km wide, is capped by at least 300 m of sediment, and contains talus aprons along its lower flanks. Ferromanganese-encrusted rocks were recovered in every dredge and are thickest on Necker Ridge. Crust thicknesses average about 2.5, 1.5, and 0.8 cm for Necker, Horizon, and S.P. Lee, respectively. Crusts range from smooth or porous surfaces to knobby and botryoidal. The entire crust is laminated, however, two distinct layers commonly exist, separated by a paper-thin layer of phosphorite. The dominant mineral of all crusts is vernadite (δ-MnO 2 ), while quartz, feldspar, apatite, and, in three rocks todorokite, are minor phases. Quartz and feldspar decrease with decreasing latitude of occurrence, and is suggested to be related to eolian input. On the average, apatite also increases within the crusts with decreasing latitude of occurrence, which may be related to high biological productivity in the zone of equatorial upwelling. Phosphorite substrates are more abundant on Necker Ridge and S.P. Lee Guyot than they are on Horizon Guyot. Seamount ferromanganese nodules are distinct from abyssal nodules in their chemistry and internal structure.