(Table 1) Summary of horizon, lithology, and paleomagnetic of ODP Hole 126-791B basaltic mousse samples

A paleomagnetic study was made on the highly vesiculated basaltic tuff breccia (the basaltic mousse) drilled by Ocean Drilling Program Leg 126 from the Izu-Bonin backarc, Sumisu Rift, to estimate the mode of its emplacement. Thirty-four 10-cm**3 minicore samples were collected from almost all the horizons of the basaltic mousse. Stepwise thermal and alternating-field demagnetization experiments show that the natural remanent magnetizations of many samples are mainly composed of a single stable component. Although remanence inclinations are not expected to be disturbed by rotary drilling, the measured inclinations of remanence show a random directional distribution as a whole. The remanence inclinations, however, show directional consistency on a smaller scale. High-density sampling and measurements from a limited interval of drilled cores, and the measurement of small disks cut from a single minicore sample show that there is directional consistency over several centimeters. Strong and stable remanent magnetization, the existence of remanence direction consistency, and the fresh lithology of the samples suggest the thermal origin of remanence. Combining the paleomagnetic results with other geological, petrographical, and paleontological characters, the Hole 791B basaltic mousse can be interpreted as a subaqueous explosion breccia produced by deep-sea pyroclastic fountaining.

Geochemistry of serpentine muds of ODP Leg 125 holes

The <63-µm fractions of serpentinite muds from two seamounts on the Mariana and Izu-Bonin forearcs were analyzed for mineral composition by X-ray diffraction and for chemical composition by X-ray fluorescence. The silt fraction of the muds consists predominantly of chrysotile, brucite, and ample amorphous constituents. Chlorite and smectite are less abundant components. Of special interest is the occurrence of iowaite, a brucite-like, Cl-bearing mineral with a layered structure. Iowaite was not found in the samples from the summit site of one of the seamounts drilled; however, it is scattered throughout the strata, composing the flanks of both seamounts investigated. No systematic change of the iowaite abundance with depth was observed. The distribution of iowaite is confined to the surface of the flanks of the seamount. Based on the distribution on the mineral and its chemical composition, we suggest that the iowaite formed by oxidation of some of the ferrous iron in brucite contained in the serpentine mud as it contacted abyssal seawater during protrusion onto the seafloor. The resulting positive charge imparted to the brucite was compensated by the uptake of seawater chloride. Consequently, the formation of iowaite is restricted to the seafloor where oxygen and chloride are available for these reactions. The availability of oxygen is considered the limiting factor. We conclude that iowaite formation cannot be a major cause for the low chlorinity of pore fluids inside the seamounts.

Geochemistry of ocean floor and forearc serpentinites

We provide new insights into the geochemistry of serpentinites from mid-ocean ridges (Mid-Atlantic Ridge and Hess Deep), passive margins (Iberia Abyssal Plain and Newfoundland) and fore-arcs (Mariana and Guatemala) based on bulk-rock and in situ mineral major and trace element compositional data collected on drill cores from the Deep Sea Drilling Project and Ocean Drilling Program. These data are important for constraining the serpentinite-hosted trace element inventory of subduction zones. Bulk serpentinites show up to several orders of magnitude enrichments in Cl, B, Sr, U, Sb, Pb, Rb, Cs and Li relative to elements of similar compatibility during mantle melting, which correspond to the highest primitive mantle-normalized B/Nb, B/Th, U/Th, Sb/Ce, Sr/Nd and Li/Y among subducted lithologies of the oceanic lithosphere (serpentinites, sediments and altered igneous oceanic crust). Among the elements showing relative enrichment, Cl and B are by far the most abundant with bulk concentrations mostly above 1000 µg/g and 30 µg/g, respectively. All other trace elements showing relative enrichments are generally present in low concentrations (µg/g level), except Sr in carbonate-bearing serpentinites (thousands of µg/g). In situ data indicate that concentrations of Cl, B, Sr, U, Sb, Rb and Cs are, and that of Li can be, increased by serpentinization. These elements are largely hosted in serpentine (lizardite and chrysotile, but not antigorite). Aragonite precipitation leads to significant enrichments in Sr, U and B, whereas calcite is important only as an Sr host. Commonly observed brucite is trace element-poor. The overall enrichment patterns are comparable among serpentinites from mid-ocean ridges, passive margins and fore-arcs, whereas the extents of enrichments are often specific to the geodynamic setting. Variability in relative trace element enrichments within a specific setting (and locality) can be several orders of magnitude. Mid-ocean ridge serpentinites often show pronounced bulk-rock U enrichment in addition to ubiquitous Cl, B and Sr enrichment. They also exhibit positive Eu anomalies on chondrite-normalized rare earth element plots. Passive margin serpentinites tend to have higher overall incompatible trace element contents than mid-ocean ridge and fore-arc serpentinites and show the highest B enrichment among all the studied serpentinites. Fore-arc serpentinites are characterized by low overall trace element contents and show the lowest Cl, but the highest Rb, Cs and Sr enrichments. Based on our data, subducted dehydrating serpentinites are likely to release fluids with high B/Nb, B/Th, U/Th, Sb/Ce and Sr/Nd, rendering them one of the potential sources of some of the characteristic trace element fingerprints of arc magmas (e.g. high B/Nb, high Sr/Nd, high Sb/Ce). However, although serpentinites are a substantial part of global subduction zone chemical cycling, owing to their low overall trace element contents (except for B and Cl) their geochemical imprint on arc magma sources (apart from addition of H2O, B and Cl) can be masked considerably by the trace element signal from subducted crustal components.

40Ar-39Ar dating of rocks drilled at sites 60-458 and 60-459

40Ar-39Ar dating of a high-MgO bronzite andesite from near the top of basement drilled at Site 458 shows the characteristic symptoms of artificially disturbed samples - i.e., an inverse staircase-type age spectrum, approximate linearity on an isochron plot, and concordance between total fusion age and isochron age. From conclusions based on other artificially disturbed samples (Ozima et al., 1979), we suggest that the reference isochron age (33.6 Ma) approximates the age of the sample. A basalt from deeper in Hole 458 gives an isochron age of 19.1 ± 0.2 Ma, which is slightly younger than the plateau age of 21.4 ± 1.0 Ma. Both ages are, however, considerably younger than the age of fossils in the overlying sediments (30 - 34 Ma). The age discrepancy may be explained if the 40Ar-39Ar age represents the age of secondary minerals, which formed later. No useful age data were obtained from a basalt sample recovered from Hole 459B.