Geochemistry at DSDP Leg 92 Holes

The major-element and most of the trace-element data from the different laboratories that contributed to the study of samples recovered during Leg 82 are presented in the following tables. The different basalt groups, identified on the basis of their chemical properties (major and trace elements), were defined from the data available on board the Glomar Challenger as the cruise progressed (see site chapters, all sites, this volume). Most of the data obtained since the end of the cruise and presented in these tables confirm the classification that was proposed by the shipboard party (see site chapters, all sites, this volume). Nevertheless, special mention should be made about Site 564. The shipboard party proposed a single chemical group at this site but noticed significant variations down the hole, mainly in trace-element data. However, the range of variation was small compared to the precision of the measurements. These variations were confirmed by the onshore studies (see papers in Part IV of this volume, especially Brannon's paper, partly devoted to this topic).

Chemical and isotopic compositions of basaltic glasses and crusts from the Mid-Atlantic Ridge rift valley

Data presented in the paper suggest significant differences between thermodynamic conditions, under which magmatic complexes were formed in MAR at 29°-34°N and 12°-18°N. Melts occurring at 29°-34°N were derived by melting of a mantle source with homogeneous distribution of volatile components and arrived at the surface without significant fractionation, likely, due to their rapid ascent. The MAR segments between 12° and 18°N combine contrasting geodynamic environments of magmatism, which predetermined development of a large plume region with widespread mixing of melting products of geochemically distinct mantle sources. At the same time, this region is characterized by conditions favorable for origin of localized zones of anomalous plume magmatism. These sporadic magmatic sources were spatially restricted to MAR fragments with the Hess crust, whose compositional and mechanical properties were, perhaps, favorable for focusing and localization of plume magmatism. The plume source between 12° and 18°N beneath MAR may be geochemically heterogeneous.

Chemical composition of rocks and minerals from the Mid-Atlantic Ridge near 15°20'N

The monograph summarizes results of petrological and geochemical studies of rocks from the ocean floor collected by the authors during expeditions to the Central Atlantic. Detailed work in the Capa Verde transform fault zone gave a large amount of new information about magmatic and hydrothermal systems of the Mid-Atlantic Ridge.

Chemical composition of basalts from DSDP Hole 46-396B

Samples of crystalline basalt from Site 396 B are all more or less altered, usually in strongly zoned patterns. Evidence has been found for several related or independent alteration stages, including (1) minor localized deuteric (amphibole and mixed clay minerals in miarolitic voids); (2) minor widespread nonoxidizing (pyrite on walls of vugs and cracks); (3) localized diffusion-controlled rug filling ("glauconite" in black halos); (4) pervasive low level oxidizing (transformation of titanomagnetite to cation-deficient titanomaghemite); (5) localized diffusion-controlled strongly oxidizing (breakdown of olivine and titanomaghemite in brown zones). Plagioclase and pyroxene are essentially unaltered. Detailed analyses of gray and brown zones in pillow basalts show that low temperature oxidation has proceeded in a step-wise fashion, with the relative stabilities of the igneous minerals controlling the steps. Secondary minerals that crystallized from pore fluids on to the walls of vugs may or may not be related to local alteration of primary phases. During the most intense stage of alteration, brown oxidation zones grew into basalt fragments behind diffusion controlled fronts. The specific reactions and products of this stage differ among the lithologic units at the site. A model is proposed whereby efficient seawater circulation through the pillow units maintains the pH and the concentrations of Mg2+ and SiO2 dissolved at low levels in pore fluids, so that olivine is replaced by hydrous ferric oxides, and Mg and SiO2 are removed from the system. In the massive basalt unit, circulation is somewhat less effective and Mg and SiO2 are retained in smectites. Deposition of authigenic minerals in the sequence saponite/Fe-Mn oxides/phillipsite/calcite in vugs and cracks may reflect the gradual closing of the systems and probably signals the end of localized oxidation in parts of the core. Mineral compositions indicate that most of these deposits formed from seawater at very low temperature.

Magnetic properties of plutonic rocks at DSDP Leg 82 holes

Ten samples of gabbro and peridotite, with varying degrees of serpentinization, were studied by magnetic techniques and reflected light microscopy. Evidence from these methods suggests that the natural remanent magnetization is primarily of chemical origin. It is generally weak for the gabbros and much stronger for the peridotites. This difference is offset by the fact that the peridotites have generally lower magnetic stability and Koenigsberger ratios. There is a considerable variation in both magnetic parameters and petrology even among closely spaced samples, which suggests that some combination of source heterogeneity and tectonic mixing was involved in the production of these rocks. However, the small number of samples makes this conclusion tentative. There may also have been significant postemplacement alteration involved. All samples show a significant anisotropy of weak field susceptibility that appears to be related to deformation. This anisotropy may be useful in defining petrofabrics.

Chemistry of serpentinized peridotites from ODP Hole 109-670A

In this paper we describe textural relationships in hydrated upper mantle peridotites emplaced at a nonconstructive ridge segment. Development of serpentinites and partially serpentinized peridotites takes place in four main stages: (1) pervasive serpentinization forming mainly lizardite, (2) a tensional stage forming chrysotile + talc + chlorite, (3) a deformational stage forming antigorite + tremolite, and (4) a late local tensional stage forming another generation of chrysotile veinlets. Mineral chemistry of serpentine pseudomorphs reflects in part primary mineral compositions. Olivine pseudomorphs are typically nickeliferous and depleted in aluminum and chromium. Orthopyroxene pseudomorphs have lower nickel contents and relatively high iron, aluminum, and chromium contents. Clinopyroxene pseudomorphs have very low nickel contents and relatively high aluminum and chromium contents. These chemical patterns in the serpentinites can be used to help discriminate between harzburgitic and lherzolitic protoliths. Oxygen isotopes and mineral parageneses suggest serpentine is derived from circulation of hydrothermal (200?C) fluids through the peridotite body. Crystallization of tremolite, talc, and chlorite may have occurred at temperatures up to 525?C if C02/H20 ratios were less than 0.25. Open fissures developing in aging upper mantle provide paths for important seawater circulation through a thin basaltic carapace down to shallow mantle rocks.

Calcite composition and stable isotope record of ODP Hole 103-637A peridotites

The peridotite recovered from Ocean Drilling Program Hole 637A, Galicia margin, has suffered extensive low-temperature alteration that includes serpentinization, calcite veining, and calcite replacement. This note presents textural and geochemical data on the serpentine and calcite. Such data indicate that the serpentinization, serpentine veining, and calcite veining of the peridotite occurred in several stages late in the history of the peridotite emplacement, probably after the peridotite was emplaced at crustal levels. It is also apparent that some deformational events (evidenced by faulting and brecciation of both serpentine and calcite veins) continued after the main phase of low-temperature alteration. The geochemistry and petrology, structure, and high-temperature alteration of the peridotite are discussed in separate papers in this volume (Evans and Girardeau, 1988, doi:10.2973/odp.proc.sr.103.138.1988; Girardeau et al., 1988, doi:10.2973/odp.proc.sr.103.135.1988; Kimball and Evans, 1988, doi:10.2973/odp.proc.sr.103.140.1988; Agrinier et al., 1988, doi:10.2973/odp.proc.sr.103.136.1988).

Geochemical compositions of minerals from chilled dike margins of ODP Hole 140-504B

Mineral and whole-rock geochemical data are presented for chilled dike margins from the lower sheeted dike complex of Deep Sea Drilling Project/Ocean Drilling Program (DSDP/ODP) Hole 504B. Compositions of phenocrystic plagioclase (An80-89); olivine (Fo82-86); clinopyroxene (Wo52En40Fs8, with Cr2O3 up to 1.2%); and rare chromian spinel (Cr# 43) are consistent with those from the lavas and the upper dike complex recovered previously (DSDP Legs 69, 70, 83, and ODP Leg 111). Major and trace element compositions fall in group D of Autio and Rhodes (1983) and have high CaO/Na2O, and low TiO2, K2O, and (La/Sm)N values consistent with previous analyses from this site.

Petrographic and chemical characteristics of diabases at DSDP Holes 63-469 and 63-471

Diabasic rocks were recovered at Sites 469 and 471 on IPOD/DSDP Leg 63. The diabasic rocks are composed mainly of Plagioclase, clinopyroxene, and low-temperature alteration products. In addition to these phases, a considerable amount of primary biotite and lesser colorless amphibole are observed in some of the Site 471 diabases. Major and trace element data suggest that these rocks are tholeiitic; however, their highly altered nature obscures their petrologic affinity with the DSDP Leg 63 tholeiitic basalts and others from the nearby Pacific ocean floor. It is likely that the Site 469 and 471 diabasic rocks represent products of off-ridge intrusive activity.

(Table 1) Calcite, siderite, and stable isotopes d13C and d18O at DSDP Hole 93-603B

Diagenesis of the fine-grained, feldspathic sandstones in the Lower Cretaceous submarine fan complex cored in DSDP Hole 603B can be considered to have occurred in three stages: (1) replacement of matrix and framework grains by pyrite, siderite, phillipsite (?), and particularly by ferroan calcite; (2) dissolution of ferroan calcite and feldspars to produce secondary macroporosity; and (3) development of sparse feldspar and quartz overgrowths, and authigenic modification of remnant matrix. Only ferroan calcite is a volumetrically important diagenetic mineral phase (up to 50 vol.%). Matrix in thin sandstone turbidite deposits has been extensively replaced by ferroan calcite. Carbon stable isotope data suggest that organic diagenesis had only a minor influence on calcite precipitation. Oxygen stable isotope data indicate that the minimum average calcite precipitation temperature was 40° C. Preliminary calculations show that steadystate diffusion of Ca+ + from the dissolution of nannoplankton skeletal material in the interbedded pelagic marls to the associated sandstones is a feasible transport mechanism. A thick sandstone unit from 1234-1263 m sub-bottom is extensively replaced by calcite near the upper and lower contacts. Farther into the sand body away from the contacts, the sandstone has good secondary porosity resulting from the dissolution of ferroan calcite that partially replaced matrix and framework grains. The central portion of the thick sand appears to be a channel with high-energy clean sand. We believe that the channel provided a conduit for focused flow of diagenetic compactional fluids responsible for dissolution. Focused flow may be the result of the earlier lithification of the pelagic limestones and thin-bedded sandstones which, then formed vertical permeability barriers. Calcite dissolution has occurred and may still be occurring at temperatures less than 65°C.