1000 resultados para plagioclase xenocryst


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A geochemical, mineralogical, and isotopic database comprising 75 analyses of Ocean Drilling Program (ODP) Leg 193 samples has been prepared, representing the variable dacitic volcanic facies and alteration types observed in drill core from the subsurface of the PACMANUS hydrothermal system (Table T1. The data set comprises major elements, trace and rare earth elements (REE), various volatiles (S, F, Cl, S, SO4, CO2, and H2O), and analyses of 18O and 86Sr/87Sr for bulk rock and mineral separates (anhydrite). Furthermore, normative mineral proportions have been calculated based on the results of X-ray diffraction (XRD) analysis (Table T2) using the SOLVER function of the Microsoft Excel program. Several of the samples analyzed consist of mesoscopically distinctive domains, and separate powders were generated to investigate these hand specimen-scale heterogeneities. Images of all the samples are collated in Figure F1, illustrating the location of each powder analyzed and documenting which measurements were performed.

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Several distinct, thin (2-7 cm), volcanic sand layers ("ashes") were recovered in the upper portions of Holes 842A and 842B. These holes were drilled 320 km west of the island of Hawaii on the outer side of the arch that surrounds the southern end of the Hawaiian chain. These layers are Pliocene to Pleistocene in age, graded, and contain fresh glass and mineral fragments (mainly olivine, plagioclase, and clinopyroxene) and tests of Pleistocene to Eocene radiolarians. The glass fragments are weakly vesicular and blocky to platy in shape. The glass and olivine fragments from individual layers have large ranges in composition (i.e, larger than expected for a single eruption). These features are inconsistent with an explosive eruption origin for the sands. The only other viable mechanism for transporting these sands hundreds of kilometers from their probable source, the Hawaiian Islands, is turbidity currents. These currents were probably related to several of the giant debris slides that were identified from Gloria sidescan images around the islands. These currents would have run over the ~500-m-high Hawaiian Arch on their way to Site 842. This indicates that the turbidity currents were at least 325 m thick. Paleomagnetic and biostratigraphic data allow the ages of the sands to be constrained and, thus, related to particular Hawaiian debris flows. These correlations were checked by comparing the compositions of the glasses from the sands with those of glasses and rocks from islands with debris flows directed toward Site 842. Good correlations were found for the 110-ka slide from Mauna Loa and the ~1.4-Ma slide from Lanai. The correlation with Kauai is poor, probably because the data base for that volcano is small. The low to moderate sulfur content of the sand glasses indicates that they were derived from moderately to strongly degassed lavas (shallow marine or subaerially erupted), which correlates well with the location of the landslide scars on the flanks of the Hawaiian volcanoes. The glass sands may have been formed by brecciation during the landslide events or spallation and granulation as lava erupted into shallow water.

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Results of investigations of Baikal bottom sediments from a long core (BDP-97) and several short (0-1 m) cores are presented. It can be shown that Holocene sediments in the Baikal basins consist of biogenic-terrigenous muds accumulated under still sedimentation conditions, and of turbidites formed during catastrophic events. The turbidites can be distinguished from the host sediments by their enrichment in heavy minerals and thus their high magnetic susceptibility. Often, Pliocene and Pleistocene diatom species observed in the Holocene sediments (mainly in the turbidites) point to redeposition of ancient offshore sediments. Our results indicate that deltas, littoral zones, and continental slopes are source areas of turbidites. The fact that the turbidites occur far from their sources confirms existence of high-energy turbidity currents responsible for long-distance lateral-sediment transport to the deep basins of the lake.

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The relatively fresh basement basaltic rocks cored at Sites 794 and 797 during ODP Legs 127 and 128 show compositional variations suggesting the following: (1) the aphyric rocks might be differentiated from compositional equivalents of the aphyric sample with the lowest FeO*/MgO (Sample 127-797C-12R-4, 35-37 cm); and (2) the plagioclase-phyric rocks (i.e., another constituent of the basement basaltic rocks from the sites) may be derivatives from the same parents; in this case, however, crystallized plagioclase was not effectively removed. Melting experiments were conducted for Sample 127-797C-12R-4, 35-37 cm, and the differentiation processes for the basement basaltic rocks were assessed. The high-pressure melting-phase relation can not account for the compositional variation of the aphyric rocks, suggesting that the variation was developed at relatively low pressure where olivine and plagioclase fractionation was followed by Ca-rich clinopyroxene fractionation. The density of Sample 127-797C-12R-4,35-37 cm, is comparable to that of plagioclase at some depth, but at still relatively low pressure, making it possible that the liquidus plagioclase was retained in the successive liquids to produce the plagioclase-phyric rocks. According to backtrack calculation assuming the olivine maximum fractionation, Sample 127-797C-12R-4, 35-37 cm, was differentiated from primary picritic high-Al basalt magma. The estimated primary magma composition was experimentally proved to coexist with harzburgite mantle at about 14 kbar, suggesting relatively shallow production (approximately 40-50 km below surface) of the rifting-related primary magma.

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This paper provides a brief, descriptive, sedimentological background for the chapters on hydraulic piston core Site 480 in this symposium, and supplements data given in the site chapter for Sites 479-480 (this volume, Pt. 1). Sediments are composed primarily of planktonic diatoms, with minor numbers of silicoflagellates, radiolarians, and varying amounts of both benthic and planktonic foraminifers, along with a large terrigenous component of olive brown, silty clay. The section contains meter-thick intervals of finely laminated facies alternating with nonlaminated zones. A few paleoenvironmental events are documented within the generally uniform sequence by sporadic occurrences of thin turbidites, phosphatic concretions, fish debris concentrations, an ash layer, and a thin layer of diagenetic dolomite. The distribution of nonlaminated and laminated zones is attributed to fluctuations of bottom-water oxygen content caused by variations in circulation, fertility, and productivity. Homogeneous sections are interpreted as coinciding with cooler climatic periods, whereas laminated sections seem to correspond to upwelling conditions during drier periods.

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Tholeiitic basalts were obtained from basaltic basement ranging in age from 6 to 17 m.y. on IPOD/DSDP Leg 63. The main rock types encountered at all sites but 473 are basaltic pillow lavas. Although many of these pillow basalts are highly or moderately altered, fresh glass is usually present. At Site 473, we recovered coarse-grained, massive basalts; no clearly defined pillowed forms were observed. Phenocrysts or microphenocrysts present in the Leg 63 basalts are Plagioclase and clinopyroxene at Site 469; olivine, Plagioclase, and spinel at Site 470; and olivine, Plagioclase, and clinopyroxene at Sites 472 and 473. Olivines of the basalts from Holes 470A and 472 (Fo85-88) are generally more magnesian than those of the Hole 473 basalts (Fo77-81). Also, plagioclases of Holes 470A and 472 basalts (An70-85) are generally more calcic than those of Holes 469 and 473 basalts (An66-72). Geochemical study of the Leg 63 basalts indicates that in all cases they are large-ion-lithophile (LIL) element depleted tholeiites like typical abyssal tholeiites. In particular, they are very similar in composition to those described from the eastern Pacific, although the degree of iron enrichment found in the Leg 63 basalts is not as extensive as in basalts from the Galapagos spreading center. Hence, the geochemical evidence of the Leg 63 basalts is compatible with their formation at a spreading center. Compositional variations in Leg 63 basalts from any single drill hole is small. Major and trace element data indicate that the samples from Holes 469 and 473 are more fractionated in chemical composition than are the samples from Holes 470A and 472; this compositional variation may be largely ascribed to differences in the extent of shallow-level fractional crystallization of similar parental magma. The Hole 472 samples, however, show a LIL element character distinct from the other Leg 63 samples.

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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.

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An investigation of recent bottom sediments between the Cyprus Island and the Syrian seacoast during Cruise 27 of R/V Vityaz-2 (1993) gave comprehensive field data significantly complementing our understanding of the sedimentation process in this part of the Mediterranean Sea. Mineralogical and geochemical indicators testify to different input into sedimentation of the Syrian and Nile River sources. The Nile River plays a leading role in terrigenous sedimentation in the southeastern Mediterranean Sea, especially in deep-sea areas. In contrast, contribution of weathering products of basalts and ophiolites from the Syrian drainage area (hornblende, monoclinic and rhombic pyroxenes, olivine, spinel, palagonite, and epidote) are particularly detectable in sediments of the near-coast zone. During Late Quaternary contribution of terrigenous material both from the Syrian and Nile sources was irregular in time.

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Acid-sulfate alteration of basalt by SO2-bearing volcanic vapors has been proposed as one possible origin for sulfate-rich deposits on Mars. To better define mineralogical signatures of acid-sulfate alteration, laboratory experiments were performed to investigate alteration pathways and geochemical processes during reaction of basalt with sulfuric acid. Pyroclastic cinders composed of phenocrysts including plagioclase, olivine, and augite embedded in glass were reacted with sulfuric acid at 145 °C for up to 137 days at a range of fluid : rock ratios. During the experiments, the phenocrysts reacted rapidly to form secondary products, while the glass was unreactive. Major products included amorphous silica, anhydrite, and Fe-rich natroalunite, along with minor iron oxides/oxyhydroxides (probably hematite) and trace levels of other sulfates. At the lowest fluid : rock ratio, hexahydrite and an unidentified Fe-silicate phase also occurred as major products. Reaction-path models indicated that formation of the products required both slow dissolution of glass and kinetic inhibitions to precipitation of a number of minerals including phyllosilicates and other aluminosilicates as well as Al- and Fe-oxides/oxyhydroxides. Similar models performed for Martian basalt compositions predict that the initial stages of acid-sulfate alteration of pyroclastic deposits on Mars should result in formation of amorphous silica, anhydrite, Fe-bearing natroalunite, and kieserite, along with relict basaltic glass. In addition, analysis of the experimental products indicates that Fe-bearing natroalunite produces a Mössbauer spectrum closely resembling that of jarosite, suggesting that it should be considered an alternative to the component in sulfate-rich bedrocks at Meridiani Planum that has previously been identified as jarosite.

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Numerous fresh ash layers comprise about 0.3% by volume of Neogene to Holocene sediments drilled at Leg 104 Sites 642 and 643 (Vøring Plateau, North Atlantic). Median grain sizes of the ashes are about 100 /µm and maximum grain sizes range up to 1200 µm. Rhyolitic pumice shards dominate, with minor bubble wall shards. Basaltic shards are poorly vesicular and blocky or round. Phenocrystic plagioclase, zircon, and clinopyroxene occur in the rhyolitic, plagioclase, and clinopyroxene phenocrysts and basaltic lithics in the basaltic tephra. Quartz, amphibole, clinozoisite, and rutile are interpreted as xenocrysts. All ash layers are well-sorted and represent distal fallout from major explosive eruptions. Most ashes are rhyolitic (high-K and low-K) in composition, some are bimodal (tholeiitic and rhyolitic). Early Miocene tephra is dominantly basaltic. Iceland is inferred to be the likely source region for most ashes. Late Miocene high-K rhyolites may have originated from the K-rich Jan Mayen magmatic province. One Quaternary layer with biotite and alkali feldspar phenocrysts may have been derived from Jan Mayen Island. Four individual Pliocene to Holocene ash layers from Sites 642 and 643 can be correlated fairly well. Upper Miocene layers are tentatively correlated as a sequence between Sites 642 and 643. Average calculated layer frequencies are about three layers/m.y. through the Pliocene and Pleistocene and five to eight layers per m.y. through the middle and late Miocene, suggesting rather continuous volcanic activity in the North Atlantic. Episodic magmatic activity during Neogene epochs in this part of the North Atlantic, as postulated in the literature, cannot be confirmed.

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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.

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Gabbros drilled from the shallow (720 m) east wall of the Atlantis II transform on the Southwest Indian Ridge (SWIR; 32°43.40', 57°16.00') provide the most complete record of the stratigraphy and composition of the oceanic lower crust recovered from the ocean basins to date. Lithologies recovered include gabbro, olivine gabbro, troctolite, trondhjemite, and unusual iron-titanium (FeTi) oxide-rich gabbro containing up to 30% FeTi oxides. The plutonic rock sequence represents a tholeiitic fractionation trend ranging from primitive magmas having Mg numbers of 67 to 69 that fractionated troctolites, to highly evolved liquids that crystallized two-pyroxene, FeTi oxide-rich gabbros and, ultimately, trondhjemite. Isotopic compositions of unaltered Leg 118 gabbros are distinct from Indian Ocean mid-ocean ridge basalts (MORB) in having higher 143Nd/144Nd (0.51301-0.51319) and lower 206Pb/204Pb values (17.35-17.67); 87Sr/86Sr values (0.7025-0.7030) overlap those of SWIR basalts, but are generally lower than MORBs from the Southeast Indian Ridge or the Rodrigues Triple Junction. More than one magma composition may have been introduced into the magma chamber during its crystallization history, as suggested by the higher 87Sr/86Sr, 206Pb/204Pb, and lower 143Nd/144Nd values of chromium-rich olivine gabbros from the bottom of Hole 735B. Whole-rock gabbro and plagioclase mineral separate 87Sr/86Sr values are uniformly low (0.7027-0.7030), irrespective of alteration and deformation. By contrast, 87Sr/86Sr values for clinopyroxene (0.7025-0.7039) in the upper half of Hole 735B are higher than coexisting plagioclase and reflect extensive replacement of clinopyroxene by amphibole. Hydrothermal veins and breccias have elevated 87Sr/86Sr values (0.7029-0.7035) and indicate enhanced local introduction of seawater strontium. Oxygen- and hydrogen-isotope results show that secondary amphiboles have uniform dD values of -49 to -54 per mil and felsic hydrothermal veins range from -46 to - 77 per mil. Oxygen-isotope data for secondary amphibole and visibly altered gabbros range to low values (+1.0-+5.5 per mil), and O-isotope disequilibrium between coexisting pyroxene and plagioclase pairs from throughout the stratigraphic column indicates that seawater interacted with much of the gabbro section, but at relatively low water/rock ratios. This is consistent with the persistence of low 87Sr/86Sr values, even in gabbros that were extensively deformed and altered.