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Frederick A. Frey

Publications and source records attributed to Frederick A. Frey.

3 recordsLinked to original sources

Controls on ferromanganese crust composition and reconnaissance resource potential, Ninetyeast Ridge, Indian Ocean

A reconnaissance survey of Fe-Mn crusts from the 5000 km long (~31°S to 10°N) Ninetyeast Ridge (NER) in the Indian Ocean shows their widespread occurrence along the ridge as well as with water depth on the ridge flanks. The crusts are hydrogenetic based in growth rates and discrimination plots. Twenty samples from 12 crusts from 9 locations along the ridge were analyzed for chemical and mineralogical compositions, growth rates, and statistical relationships (Q-mode factor analysis, correlation coefficients) were calculated. The crusts collected are relatively thin (maximum 40 mm), and those analyzed varied from 4 mm to 32 mm. However, crusts as thick as 80 mm can be expected to occur based on the age of rocks that comprise the NER and the growth rates calculated here. Growth rates of the crusts increase to the north along the NER and with water depth. The increase to the north resulted from an increased supply of Mn from the oxygen minimum zone (OMZ) to depths below the OMZ combined with an increased supply of Fe at depth from the dissolution of biogenic carbonate and from deep-sourced hydrothermal Fe. These increased supplies of Fe increased growth rates of the deeper-water crusts along the entire NER. Because of the huge terrigenous (rivers, eolian, pyroclastic) and hydrothermal (three spreading centers) inputs to the Indian Ocean, and the history of primary productivity, Fe-Mn crust compositions vary from those analyzed from open-ocean locations in the Pacific. The sources of detrital material in the crusts changed along the NER and reflect, from north to south, the decreasing influence of the Ganga River system and volcanic arcs located to the east, with increasing influence of sediment derived from Australia to the south. In addition, weathering of NER basalt likely contributed to the aluminosilicate fraction of the crusts. The southernmost sample has a relatively large detrital component compared to other southern NER crust samples, which was probably derived predominantly from weathering of local volcanic outcrops. Fe-Mn crusts from a dredge haul at 3412 m water depth, 2°S latitude, are pervasively phosphatized along with the substrate rocks (site D7). Phosphatization took place through replacement of carbonate, preferential replacement of Fe oxyhydroxide relative to Mn oxide in the crusts, preferential replacement of silica-rich phases relative to Al-rich phases in the crusts, and precipitation of carbonate fluorapatite in pore space. The preferentially replaced silica may have been Si adsorbed on the Fe oxyhydroxide. The enrichment of Ni, Zn, and Cu in the phosphatized crust reflects preferential adsorption into the tunnel structure of todorokite. The rare earth element plus yttrium (REY) patterns indicate a lower oxidation potential during phosphatization of the NER crusts compared to Pacific phosphatized crusts. NER phosphatization occurred in a deeper-water environment than typical for phosphatization of Pacific crusts, occurred post-middle Miocene, a younger age than phosphatization the Pacific crusts, and had in part a different set of chemical changes produced by the phosphatization than did the Pacific crusts. The southern third of NER has Fe-Mn crusts with the highest Co (0.91%), Ni (0.43%), ΣREY (0.33%), Cu (0.22%), Te (146 ppm), Pt (1.5 ppm), Ru (52 ppb), and Rh (99 ppb) contents. These are among the highest Pt, Ru, and Rh concentrations measured in marine Fe-Mn deposits. Because of these high metal concentrations, exploration is warranted for the southern sector of the NER, especially at shallower-water sites where the platinum group elements (PGE) and Co are likely to be even more enriched.

Deep-Sea Research Part I: Oceanographic Research P

East Molokai and other Kea-trend volcanoes: Magmatic processes and sources as they migrate away from the Hawaiian hot spot

[1] There are geochemical differences between shield lavas from the two parallel trends, Kea and Loa, defined by young Hawaiian volcanoes. The shield of East Molokai volcano, at greater than 1.5 Ma, is the oldest volcano on the Kea trend. Sequences of older tholeiitic to younger alkalic basalt that erupted as this volcano evolved from the shield to postshield stage of volcanism are well exposed. Much younger, ∼0.34–0.57 Ma, alkalic basalt and basanite erupted during rejuvenated stage volcanism. Like rejuvenated stage lavas erupted at other Hawaiian volcanoes, rejuvenated stage East Molokai lavas have relatively low 87 Sr/ 86 Sr and high 143 Nd/ 144 Nd. Such ratios reflect a source component with a long-term depletion in abundance of incompatible elements. On the basis of positive correlations of 87 Sr/ 86 Sr versus 206 Pb/ 204 Pb and negative correlations of these isotopic ratios with Nb/Zr, a smaller proportion of this depleted component also contributed to the late shield/postshield lavas erupted at East Molokai and the other Kea-trend volcanoes, Haleakala and Mauna Kea. At each of these Kea-trend volcanoes, as the volcano moved away from the hot spot, the extent of melting and magma supply from the mantle decreased, the depth of melt segregation increased, and there was an increasing role for a component with long-term relative depletion in incompatible elements. This depleted component has Kea-trend Pb isotopic characteristics and relatively low 208 Pb/ 204 Pb at a given 206 Pb/ 204 Pb, and it is probably not related to oceanic lithosphere or the source of mid-ocean ridge basalt. The overlap in Sr, Nd, and Pb isotope ratios of recent Kilauea shield lavas and 550 ka Mauna Kea shield lavas has been used to argue that Kea-trend shield volcanism samples a vertically continuous, geochemically distinct stripe which persisted in the hot spot source for 550 kyr (Eisele et al., 2003; Abouchami et al., 2005). As Kea-trend volcanoes migrate away from the hot spot and evolve from the shield to postshield stage, there are systematic changes in Sr, Nd, and Pb isotope ratios. However, the overlap of Sr, Nd, and Pb isotope ratios in late shield/postshield lavas from Mauna Kea (<350 ka) and East Molokai (∼1.5 Ma) show that the periphery of the hot spot sampled by Kea-trend postshield lavas also had long-term geochemical homogeneity.

Hawai'i

An experimental study of the partitioning of a rare earth element (Gd) in the system diopside—Aqueous vapour

The partitioning of Gd in the experimental system diopside-aqueous vapor as a function of temperature, pressure, composition of the phases, time, grain size, solid-liquid ratio and Gd concentration has been investigated. A radioactive tracer measurement was used to determine Gd concentration in the separated phases. Diposides were reacted with aqueous vapor containing tracer Gd and reversibility was tested by reacting Gd-doped diopsides with pure aqueous vapor. Equilibration of Gd between the bulk of the diopside and the liquid was found to be limited by the slow rate of Gd diffusion in diopside, maximum value of D = 2 × 10 −15 cm 2 sec −1 at 800°C and 1 kb. Depending on whether the diopside was previously synthesized or synthesized from an oxide mix during the experiment, Gd concentrations were zoned in the crystal such that higher concentrations existed at the edges or center, respectively. Equilibrium is difficult to achieve in these experiments, but at the optimum experimental conditions for equilibration, the Gd diopside-aqueous vapor distribution coefficient is 20 ± 6 (800°C, 1 kb) in approximate agreement with previous results of 55 ± 23. Changing the composition of the aqueous vapor indicated that possible mechanisms for Gd substitution included coupling of Gd 3+ with H + or Na + replacing 2Ca 2+ , or substitution of 2Gd 3+ for 3Ca 2+ with formation of a cation vacancy.

Geochimica et Cosmochimica Acta