Chemical composition of nodules and crusts from the Sea of Japan

Iron-manganese mineralization on seamounts and rises in the Sea of Japan is represented by iron-manganese nodules and crusts. Their chemical composition (major elements and more than 30 trace elements) was studied by a series of analytical methods. According to geochemical comparisons hydrogenic, hydrothermal, and biogenic materials have participated in creation of this mineralization. Contents of Ba and Li, as well as Mo/Pb and Sb/As ratios can be used as indicators of genesis of iron-manganese nodules and crusts along with composition of the rare earth elements.

Chemical composition of smectite-bearing basal metalliferous sediments from DSDP Leg 9

The mineralogy and P, Fe and Mn contents of basal metalliferous and nonmetalliferous sediments of two Deep Sea Drilling Project cores (Sites 77 and 80) were investigated. When compared with superjacent nonmetalliferous material, basal metalliferous sediments are significantly enriched in P, Fe and Mn. Among the phases present in the metalliferous sediment samples are a poorly-crystalline Fe-rich smectite and X-ray amorphous Fe oxyhydroxides. P is associated primarily with the oxyhydroxides. Adsorption of phosphate on smectite does not seem to play any role in the uptake of P by metalliferous sediments. An estimate of the removal of P by on- and off-ridge metallogenic deposition suggests that this process strongly affects the overall geochemical balance of phosphorus in the World Ocean.

Chemical and isotopic compositions of pore fluids from ODP Sites 169-1034 and 169-1037

We have analysed the concentrations of Li, K, Rb, Cs, and B, and the isotopic ratios of Li and B of a suite of pore fluids recovered from ODP Sites 1037 (Leg 169; Escanaba Trough) and 1034 (Leg 169S; Saanich Inlet). In addition, we have analysed dissolved K, Rb, and Cs concentrations for estuarine mixing of the Ganges-Brahmaputra river system. Together, these data sets have been used to assess the role of sediments in the marine geochemical cycles of the alkali elements and boron. Uptake onto clay minerals during estuarine mixing removes 20-30% of the riverine input of dissolved Cs and Rb to the oceans. Prior to this study, the only other recognised sink of Rb and Cs was uptake during low-temperature alteration of the oceanic crust. Even with this additional sink there is an excess of inputs over outputs in their modern oceanic mass balance. Pore fluid data show that Li and Rb are transferred into marine sediments during early diagenesis. However, modeling of the Li isotope systematics of the pore fluids from Site 1037 shows that seawater Li taken up during marine sedimentation can be readily returned to solution in the presence of less hydrated cations, such as NH4+. This process also appears to result in high concentrations of pore fluid Cs (relative to local seawater) due to expulsion of adsorbed Cs from cation exchange sites. Flux calculations based on pore fluid data for a series of ODP sites indicate that early diagenesis of clay sediments removes around 8% of the modern riverine input of dissolved Li. Although NH4+-rich fluids do result in a flux of Cs to the oceans, on the global scale this input only augments the modern riverine Cs flux by ~3%. Nevertheless, this may have implications for the fate of radioactive Cs in the natural environment and waste repositories.

Particulate concentrations and vertical fluxes of sedimentary material and chemical elements, composition of particulate and sinking material in the water column of the Bear Island Trough, Norwegian Sea, July 1995

CTD and nephelometric sounding data are considered along with parameters of the near-bottom currents and particulate fluxes measured by a subsurface mooring station in the northern part of the Bear Island Trough. It is shown that the near-bottom current is characterized by highly variable parameters, while distribution of suspended particulate matter demonstrates surface and bottom maxima. Horizontal and vertical fluxes of sedimentary material in the nepheloid layer are studied.

Chemical composition of manganese nodules and crusts collected from the Hakurei Maru Cruise GH74-5 in the Eastern Central Pacific Basin

Chemical composition of manganese nodules and crust collected from the Hakurei Maru Cruise GH74-5, September-October, 1974, in the Eastern Central Pacific Basin by the Geological Survey of Japan according to: Analyses and sample manganese deposits data from Cruise GH74-5 (private communication) (unpublished), Scripps Institution of Oceanography. http://www.ngdc.noaa.gov/mgg_mmbib/showref.jsp?mmbib=MIZUAA7702.

Chemical composition of a ferromanganese crust recovred during the GH74-5 cruise of the R/V Hakurei-Maru

Data comes from the NGDC database, https://www.ngdc.noaa.gov/.

(Table 3, page 373) Chemical composition of manganese nodules from the Komahashi-Daini Seamount in the Northern Philippine Sea

Petrological, mineralogical and chemical investigations of marine manganese nodules from the West Pacific revealed the intimate relation between the chemical and mineral compositions and the remarkable preferential partitioning of metal elements in the ferromanganese minerals. The microscopic observations of textures of manganese nodules tell the growth history of manganese nodules and the formation conditions of ferromanganese minerals. Chemical compositions of nodules from Komahashi-Daini Seamount are very similar to those of the nodules from marginal banks and seamounts. Compositional variations in the bulk composition of nodules collected from the same dredge haul are considerably small, suggesting the similarity of the growth history of individual nodules, although the contents of metal elements vary remarkably from layer to layer in a single nodule.

(Table 2, Page 287) Chemical composition of manganese nodules from GH76-1 cruise

Chemical analyses of manganese nodules from the Central Pacific Basin show that their chemical composition varies regionally, although that of the associated sediments is markedly uniform throughout the basin. Mn content varies from 16 to 32% in average. Its higher value is generally found in nodules from siliceous clay and a few from deep-sea clay. Fe content tends to enrich in nodules from deep-sea clay area. Most manganese nodules, except those from deep-sea clay, are remarkably depleted in Fe compared with ones from the other Pacific regions. Mostly, Cu and Ni contents exceed 1% in nodules from siliceous clay, and decrease towards the northwest of the basin where deep-sea clay is distributed. The inter-element relationship between manganese nodules and associated sediments suggests that the mechanism of incorporation of major and minor elements in nodules is apparently different from that of the associated sediments. This finding seems to provide a new interpretation on the problem why manganese nodules having low accumulation rate are not buried by the associated sediments with greater sedimentation rate and then occur on sediment-seawater interface.

(Table 1, page 1376) Chemical analyses of manganese nodules and crusts from the Pacific Ocean

A compilation of chemical analyses of Pacific Ocean nodules using an x-ray fluorescence technique. The equipment used was a General Electric XRD-5 with a tungsten tube. Lithium fluoride was used as the diffraction element in assaying for all elements above calcium in the atomic table and EDDT was used in conjunction with a helium path for all elements with an atomic number less than calcium. Flow counters were used in conjunction with a pulse height analyzer to eliminate x-ray lines of different but integral orders in gathering count data. The stability of the equipment was found to be excellent by the author. The equipment was calibrated by the use of standard ores made from pure oxide forms of the elements in the nodules and carefully mixed in proportion to the amounts of these elements generally found in the manganese nodules. Chemically analyzed standards of the nodules themselves were also used. As a final check, a known amount of the element in question was added to selected samples of the nodules and careful counts were taken on these samples before and after the addition of the extra amount of the element. The method involved the determination and subsequent use of absorption and activation factors for the lines of the various elements. All the absorption and activation factors were carefully determined using the standard ores. The chemically analyzed samples of the nodules by these methods yielded an accuracy to at least three significant figures.

(Table 2) Chemical element contents in the surface sediment layer on the submeridional section through the Eastern Pacific

Paper devoted to geochemistry of antimony in metalliferous and transitional sediments from the Southeast Pacific.