Geochemistry of the oceanic crust from ocean drilling samples

This book presents new data on chemical and mineral compositions and on density of altered and fresh igneous rocks from key DSDP and ODP holes drilled on the following main tectonomagmatic structures of the ocean floor: 1. Mid-ocean ridges and abyssal plains and basins (DSDP Legs 37, 61, 63, 64, 65, 69, 70, 83, and 91 and ODP Legs 106, 111, 123, 129, 137, 139, 140, 148, and 169); 2. Seamounts and guyots (DSDP Legs 19, 55, and 62 and ODP Legs 143 and 144); 3. Intraplate rises (DSDP Legs 26, 33, 51, 52, 53, 72, and 74 and ODP Legs 104, 115, 120, 121, and 183); and 4. Marginal seas (DSDP Legs 19, 59, and 60 and ODP Legs 124, 125, 126, 127, 128, and 135). Study results of altered gabbro from the Southwest Indian Ridge (ODP Leg 118) and serpentinized ultramafic rocks from the Galicia margin (ODP Leg 103) are also presented. Samples were collected by the authors from the DSDP/ODP repositories, as well as during some Glomar Challenger and JOIDES Resolution legs. The book also includes descriptions of thin sections, geochemical diagrams, data on secondary mineral assemblages, and recalculated results of chemical analyses with corrections for rock density. Atomic content of each element can be quantified in grams per standard volume (g/1000 cm**3). The suite of results can be used to estimate mass balance, but parts of the data need additional work, which depends on locating fresh analogs of altered rocks studied here. Results of quantitative estimation of element mobility in recovered sections of the upper oceanic crust as a whole are shown for certain cases: Hole 504B (Costa Rica Rift) and Holes 856H, 857C, and 857D (Middle Valley, Juan de Fuca Ridge).

Petrographic description and geochemistry of basalts and altered volcanic rocks from ODP Leg 183 sites

The basalts recovered during Legs 183 and 120 from the southern, central, and northernmost parts of the Kerguelen Plateau (Holes 1136A, 1138A, 1140A, and 747C, respectively), as well as those recovered from the eastern part of the crest of Elan Bank (Hole 1137A), represent derivates from tholeiitic melts. In the northern part of the Kerguelen Plateau (Hole 1140A), basalts may have formed from two sources located at different depths. This is reflected in the presence of both low- and high-titanium basalts. The basalts are variably altered by low-temperature hydrothermal processes (at temperatures up to 120°C), and some are affected by subaerial weathering. The hydrothermal alteration led mainly to the formation of smectites, chlorite minerals, mixed-layer hydromica-smectite and smectite-chlorite minerals, hydromica, serpentine(?), clinoptilolite, heulandite, stilbite, analcime, mordenite, thomsonite, natrolite(?), calcite, quartz, and dickite(?). Alteration of extrusive basalts is mainly related to horizontal fluid flow within permeable contact zones between lava flows. Under a nonoxidizing environment of alteration, the tendency to lose most of elements, including rare earth elements, from basalts dominates. Under on oxidizing environment, basalts accumulate many elements.

Primary composition, alteration, and origin of Cretaceous volcaniclastic rocks at DSDP Site 89-585

An upper Aptian to middle Albian series of volcaniclastic rocks more than 300 m thick was drilled at Site 585 in the East Mariana Basin. On the basis of textural and compositional (bulk-rock chemistry, primary and secondary mineral phases) evidence, the volcaniclastic unit is subdivided into a lower (below 830 m sub-bottom) and an upper (about 670-760 m) sequence; the boundary in the interval between is uncertain owing to lack of samples. The rocks are dominantly former vitric basaltic tuffs and minor lapillistones with lesser amounts of crystals and basaltic lithic clasts. They are mixed with shallow-water carbonate debris (ooids, skeletal debris), and were transported by mass flows to their site of deposition. The lower sequence is mostly plagioclase- and olivine-phyric with lesser amounts of Ti-poor clinopyroxene. Mineralogical and bulk-rock chemical data indicate a tholeiitic composition slightly more enriched than N-MORB (normal mid-ocean ridge basalt). Transport was by debris flows from shallow-water sites, as indicated by admixed ooids. Volcanogenic particles are chiefly moderately vesicular to nonvesicular blocky shards (former sideromelane) and less angular tachylite with quench plagioclase and pyroxene, indicating generation of volcanic clasts predominantly by spalling and breakage of submarine pillow and/or sheet-flow lavas. The upper sequence is mainly clinopyroxene- and olivine-phyric with minor plagioclase. The more Ti-rich clinopyroxene and the bulk-rock analyses show that the moderately alkali basaltic composition throughout is more mafic than the basal tholeiitic sequence. Transport was by turbidity currents. Rounded epiclasts of crystalline basalts are more common than in the lower sequence, and, together with the occurrence of oxidized olivine pseudomorphs and vesicular tachylite, are taken as evidence of derivation from eroded subaerially exposed volcanics. Former sideromelane shards are more vesicular than in the lower sequence; vesicularity exceeds 60 vol.% in some clasts. The dominant clastic process is interpreted to be by shallow-water explosive eruptions. All rocks have undergone low-temperature alteration; the dominant secondary phases are "palagonite," chlorite/smectite mixed minerals, analcite, and chabazite. Smectite, chlorite, and natrolite occur in minor amounts. Phillipsite is recognized as an early alteration product, now replaced by other zeolites. During alteration, the rocks have lost up to 50% of their Ca, compared with a fresh shard and fresh glass inclusions in primary minerals, but have gained much less K, Rb, and Ba than expected, indicating rapid deposition prior to significant seafloor weathering.

Chemistry of zeolithe and clays from Central Kerguelen Plateau basalts

Ocean Drilling Program Leg 120 recovered basement samples that consisted of zeolite-facies metabasalts at Sites 747, 749, and 750 on the Kerguelen Plateau. These basalts were metamorphosed in the low to intermediate zones of the zeolite facies, as indicated by the presence of diagnostic zeolites and the absence of chlorite, epidote, prehnite, pumpellyite, and wairakite. Chabazite, natrolite, thompsonite, mesolite, stilbite, huelandite, and smectites occur as amygduloidal fillings in basalts from Holes 747C and 750B, whereas only stilbite, laumontite, and pure and mixed-layered smectites were identified in amygduloidal basalts from Hole 749C. In the lower sections of Hole 749C, only laumontite and mixed-layered smectites coexist. Based on calculations with published experimental phase equilibria, the absence of wairakite in basalts from Hole 749C and of laumontite in basalts from Holes 747C and 750B suggests that metamorphic temperatures did not exceed approximately 225° and 120°C, respectively. The presence of well-developed zeolite mineral assemblages and the absence of carbonate and clay mineral assemblages restricts XCO2 in the fluid to approximately <=0.0075. Low- to intermediate-zone zeolite-facies mineral assemblages in basalts from the Kerguelen Plateau can be accounted for by metamorphism in an active geothermal area such as present-day Iceland.

Isotopic ratios and geochemical composition of ODP Hole 176-735B minerals

The mineralogy and stable (O and C) and Sr isotopic compositions of low-temperature alteration phases were determined in Hole 735B gabbroic rocks in order to understand the processes of low-temperature alteration in this uplifted block of lower oceanic crust. Phyllosilicates include smectite (saponite, Mg montmorillonite, and nontronite), chlorite/smectite, chlorite, talc, and serpentine. Other phases include prehnite, albite, K-feldspar, analcite, natrolite, thompsonite, pyrite, and titanite. The low-grade mineral assemblages mainly represent zeolite facies and lower-temperature "seafloor weathering" processes. Phyllosilicates formed over a range of temperatures but may also reflect variable reaction progress. Alteration temperatures were probably somewhat greater below 1300 meters below seafloor. Mineralogy and isotopic data indicate that conditions were mostly reducing and that seawater solutions were rock dominated. Carbonates formed late from cold and generally oxidizing seawater solution, however, as seawater penetrated downward as the result of fracturing and faulting in the uppermost portion of the uplifted crustal block.

Secondary minerals and geochemistry at DSDP Legs 68 and 69

Basalt samples recovered during DSDP Legs 68, 69, and 70 from a 550-meter-thick section in two holes near the Costa Rica Rift (Holes 501 and 504B) were found to contain the following secondary minerals: trioctahedral and dioctahedral smectite, chlorite, mixed-layer clays, talc, hematite, pyrite, foujasite, phillipsite, analcime, natrolite, thomsonite, gyrolite, aragonite, calcite, anhydrite, chalcocite, Fe-hydrosilicate, okenite, apophyllite, actinolite, cristobalite, quartz, and magnesite. A less positive identification of bismutite was made. A mineral rich in Mn and minerals with strong reflections at 12.9 Å and 3.20 Å remain unidentified. Trioctahedral smectite replaces glass and olivine in the basalt groundmass. The other secondary minerals occur in veins. The distribution of the secondary minerals in the basalt section shows both hydrothermal and oxidizing-nonoxidizing zonation. Most of the secondary minerals formed under alkaline, nonoxidizing conditions at temperatures up to 120° C. An acidic regime probably existed in the lowest portion of basalt. Oxidative diagenesis followed nonoxidative diagenesis in the upper part of the section. Oxidative diagenesis is characterized by the absence of celadonite, rare occurrences of dioctahedral smectite, and widespread hematite and phillipsite.

Chemistry of gabbroic rocks from ODP Hole 118-735B

Gabbroic rocks and their late differentiates recovered at Site 735 represent 500 m of oceanic layer 3. The original cooling of a mid-ocean ridge magma chamber, its penetration by ductile shear zones and late intrusives, and the subsequent penetration of seawater through a network of cracks and into highly permeable magmatic hydrofracture horizons are recorded in the metamorphic stratigraphy of the core. Ductile shear zones are characterized by extensive dynamic recrystallization of primary phases, beginning in the granulite facies and continuing into the lower amphibolite facies. Increasing availability of seawater during dynamic recrystallization is reflected in depletions in 18O, increasing abundance of amphibole of variable composition and metamorphic plagioclase of intermediate composition, and more complete coronitic or pseudomorphous static replacement of magmatic minerals. Downcore correlation of synkinematic assemblages, bulk-rock oxygen isotopic compositions, and vein abundance suggest that seawater is introduced into the crust by way of small cracks and veins that mark the end of the ductile phase of deformation. This "deformation-enhanced" metamorphism dominates the upper 180 and the lower 100 m of the core. In the lower 300 m of the core, mineral assemblages of greenschist and zeolite facies are abundant within or adjacent to brecciated zones. Leucocratic veins found in these zones and adjacent host rock contain diopside, sodic plagioclase, epidote, chlorite, analcime, thomsonite, natrolite, albite, quartz, actinolite, sphene, brookite, and sulfides. The presence of zircon, Cl-apatite, sodic plagioclase, sulfides, and diopside in leucocratic veins having local magmatic textures suggests that some of the veins originated from late magmas or from hydrothermal fluids exsolved from such magmas that were subsequently replaced by (seawater-derived) hydrothermal assemblages. The frequent association of these late magmatic intrusive rocks within the brecciated zones suggests that they are both artifacts of magmatic hydrofracture. Such catastrophic fracture and hydrothermal circulation could produce episodic venting of hydrothermal fluids as well as the incorporation of a magmatically derived hydrothermal component. The enhanced permeability of the brecciated zones produced lower temperature assemblages because of larger volumes of seawater that penetrated the crust. The last fractures were sealed either by these hydrothermal minerals or by late carbonate-smectite veins, resulting in the observed low permeability of the core.

Major elements oxides and mineralogy of primary minerals in ODP Hole 195-1201D basalts

The basement cored at Site 1201 (west Philippine Basin) during Ocean Drilling Program Leg 195 consists of a 91-m-thick sequence of basalts, mostly pillow lavas and perhaps one sheet lava flow, with a few intercalations of hyaloclastite and interpillow sedimentary material. Hydrothermal alteration pervasively affected the basalt sequence, giving rise to a variety of secondary minerals such as K-Fe-Mg-clay minerals, oxyhydroxides and clay minerals mixtures, natrolite group zeolites, analcite, alkali feldspar, and carbonate. The primary minerals of pillow and sheet basalts that survived the intense hydrothermal alteration were investigated by electron microprobe with the aim of characterizing their chemical composition and variability. The primary minerals are mostly plagioclase, ranging in composition from bytownite through labradorite to andesine, chromian-magnesian-diopside, and spinels, both Ti magnetite (partially maghemitized) and chromian spinel. Overall, the chemical features of the primary minerals of Site 1201 basalts correspond to the primitive character of the bulk rocks, suggesting that the parent magma of these basalts was a mafic tholeiitic magma that most likely only suffered limited fractional crystallization and crystallized at high temperatures (slightly below 1200°C) and under increasing fO2 conditions. The major element composition of clinopyroxene suggests a backarc affinity of the mantle source of Site 1201 basement.

Chemical and mineral compositions of basalts from the Pacific Ocean, DSDP data

Mineral and chemical alterations of basalts were studied in the upper part of the ocean crust using data of deep-sea drilling from D/S Glomar Challenger in the main structures of the Pacific floor. Extraction of majority of chemical elements (including heavy metals) from basalts results mainly from their interaction with heated sea water. As a result mineralized hydrothermal solutions are formed. On entering the ocean they influence greatly on ocean sedimentation and ore formation.

Chemistry of altered basaltic glass shards and zeolites of volcaniclastic sediments from ODP Hole 157-953C

Trace element concentrations of altered basaltic glass shards (layer silicates) and zeolites in volcaniclastic sediments drilled in the volcanic apron northeast of Gran Canaria during Ocean Drilling Program (ODP) leg 157 document variable element mobilities during low-temperature alteration processes in a marine environment. Clay minerals (saponite, montmorillonite, smectite) replacing volcanic glass particles are enriched in transition metals and rare earth elements (REE). The degree of retention of REE within the alteration products of the basaltic glass is correlated with the field strength of the cations. The high field-strength elements are preferentially retained or enriched in the alteration products by sorption through clay minerals. Most trace elements are enriched in a boundary layer close to the interface mineral-altered glass. This boundary layer has a key function for the physico-chemical conditions of the subsequent alteration process by providing a large reactive surface and by lowering the fluid permeability. The release of most elements is buffered by incorporation into secondary precipitates (sodium-rich zeolites, phillipsite, Fe- and Mn-oxides) as shown by calculated distribution coefficients between altered glasses and authigenic minerals. Chemical fluxes change from an open to a closed system behavior during prograde low-temperature alteration of volcaniclastic sediments with no significant trace metal flux from the sediment to the water column.

Composition of ODP Leg 126 sandstones

Early diagenesis in Leg 126 forearc and backarc sands/sandstones is characterized by the dissolution of intermediate to mafic brown glass, the alteration of colorless rhyolitic glass to clay minerals, precipitation of thin clay-mineral rim cements, and minor precipitation of clinoptilolite cements. Later, more intense diagenesis is restricted to Oligocene forearc basin sediments at Sites 787,792, and 793. In these sections, the effects of early diagenesis have been intensified and overprinted by later diagenetic effects including (1) large-scale dissolution of feldspar and pyroxene crystals, (2) further dissolution of vitric components, (3) precipitation of minor carbonate cements, and (4) pervasive, multiple-staged zeolite cementation. Zeolite minerals present include analcite, mordenite, natrolite, heulandite, wairakite, chabazite, erionite, herschelite, and phillipsite. The latest diagenetic events appear to be the minor dissolution of zeolite cements and the precipitation of minor carbonate and potassium feldspar(?) cements. Observed porosity types include primary interparticles; primary intraparticles in vesicular glass and foraminifers; primary interparticles reduced by compaction and cementation; secondary intraparticles produced by dissolution of feldspar, nonopaque heavy minerals, volcanic glass, and foraminifer tests; and secondary interparticles produced by the dissolution of zeolite cements. Within forearc Oligocene sections at Sites 787 and 792, diagenetic effects appear to decrease with depth in the Oligocene section; however, at Site 793 the majority of samples are intensely altered.