Petrology and geochemistry of the basement boninite series of ODP Site 125-786

The 720 m of igneous basement that was penetrated at Site 786 of Ocean Drilling Program Leg 125 consists of boninite-series volcanics. Bronzite andesites dominate the lithology and primitive magmas of high-Ca, intermediate-Ca, and low-Ca boninite are present in subordinate amounts. Sparsely phyric boninites typically contain olivine and orthopyroxene phenocrysts with Mg numbers [= Mg/(Mg + Fe) in moles] between 86% and 87%. Their high whole-rock Mg numbers, and the absence of zonation in the phenocrysts, imply equilibration at temperatures probably between 1200° and 1250°C, and 20° to 50°C below their liquidus. Equilibrium olivine and orthopyroxene have identical Mg numbers, and Mg/Fe partitioning between these minerals and the melt thus can be described with a single Kd. The invariably phenocryst-rich bronzite andesites contain Plagioclase that has spectacular zoning and mafic phases that can be as magnesian as those of the boninite parent. The most evolved melts are rhyolites with hypersthene, Plagioclase (An50), and magnetite. Eruption temperatures for the rhyolites are estimated at about 1000°C. Some magmas contain ferroactinolite in the groundmass, which is most likely a secondary, low-temperature phase. The locally large contrasts in degree of alteration are consistent with multiple episodes of magmatic activity. However, all igneous events produced boninite volcanics. Only the first, the edifice-building episode, gave rise to differentiated magmas. Differentiation of parental boninites took place by limited fractional crystallization, producing bronzite andesites. The erupted andesites, dacites and rhyolites are filter pressed extracts from these bronzite andesite magmas, which, as a result, have accumulated crystals. Subsequent younger igneous events produced high-Ca and intermediate-Ca boninites which intruded as dikes and sills throughout the basement sequence. The mineralogy of the dikes and sills reflects variable degrees of subliquidus cooling of the magma before emplacement.

Chemistry of basalts of ODP Hole 111-504B

The effect of oxygen fugacity (fO2) on the partition relationship of Mg and Fe between Plagioclase and sillicate liquid was investigated at 1 atm for basaltic samples recovered during ODP Leg 111 from Hole 504B. Samples 111-504B-143R-2 (Piece 8) and 111-504B-169R-1 (Piece 1) have Plagioclase as the liquidus phase. The distribution coefficient of Mg between Plagioclase and melt is constant at about 0.04 against the variation of fO2, whereas that of Fe (total Fe) varies from 0.3 at f(O2) = 0.2 atm to 0.03 at f(o2) = 10**-11.5 at 1200°C. The distribution coefficient of Mg is slightly higher than that calculated from the phenocryst and bulk-rock compositions, suggesting a kinetic disequilibrium effect on the distribution of Mg in Plagioclase. Because Mg, Fe, and Fe3+ have similar diffusion coefficients in silicate melt, the disequilibrium effect is greatly reduced for the exchange reaction of Mg and total Fe between Plagioclase and liquid. The exchange partition coefficient is highly dependent on fo2, with log fo2 ranging from -0.7 to - 11.5 at approximately 1200°C. Using this relationship, the f(O2) of crystallization of the magmas is estimated to be near the one defined by the fayalite-quartz-magnetite assemblage.

Petrology of high-MgO bronzite andesite resembling boninite at DSDP Hole 60-458

A high-MgO andesite which is texturally similar to boninite and a variolitic basalt collected from Site 458, about 100 km west of the Mariana Trench, have been studied through microprobe analyses and melting experiments at high water pressures. The boninite-type andesite is very similar in composition and texture to a boninite from Bonin Islands, except that the former is more calcic than the latter. The variolitic basalt contains magnesian pigeonite (Ca12Mg74Fe14) in cores of augite microphenocrysts. This pigeonite crystallized at temperatures above 1200°C. In the melting experiments of the boninite-type rock, clinopyroxene crystallizes as a liquidus phase at pressures at least above 8 kbar. No olivine crystallizes near the liquidus temperatures, indicating that the magma of this rock cannot be in equilibrium with the upper mantle periodotite (lherzolite) at depths at least greater than 25 km. The boninite-type rock is probably a product of fractional crystallization of a more primitive magma (e.g., olivine-bearing boninite magma) by separation of olivine and orthopyroxene. The magma of the variolitic basalt also cannot be in equilibrium with the upper mantle peridotite, and may be a product of fractional crystallization of a more primitive basaltic magma.

Experimental petrology of basement basaltic rocks from ODP Leg 127/128 samples

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.

(Table 1) Geochemistry of sector-zoned crystal at DSDP Hole 45-395A

Variations in crystal morphologies in pillow basalts and probable sheet flows sampled from the region of the East Pacific Rise drilled during Leg 54 are related both to differences in composition and to an extreme range of cooling rate experienced upon extrusion. The basalts range in composition from olivine-rich tholeiites to tholeiitic ferrobasalts, and include some more alkaline basalts. The kinetics of crystal growth in some samples appears to have been influenced by the amount of initial superheating (or supercooling) of the magma, or possibly by differential retention of volatiles. Olivine in quartznormative ferrobasalts apparently formed metastably at high undercooling. Despite these effects, reliable petrographic criteria are established to distinguish the principal rock types described regardless of the crystallinity and grain size. Microphenocrysts formed prior to pillow formation correspond closely to mineral assemblages inferred from normative plots and variation diagrams to control crystal fractionation at various stages. The details of spherulitic and dendritic growth also provide some clues about composition. Petrographic evidence for magma mixing is scant. Only some Siqueiros fracture zone basalts contain zoned plagioclase phenocrysts with glass inclusions similar to those used to infer mixing among Mid-Atlantic Ridge basalts. All basalts from the summit and flanks of the East Pacific Rise are aphyric. One possible petrographic consequence of mixing between olivine tholeiites and ferrobasalts - formation of clinopyroxene phenocrysts - is not evident in any fracture zone or Rise crest basalt. Highly evolved ferrobasalts with liquidus low-Ca clinopyroxene have not been sampled, nor does textural evidence indicate that any basalts sampled are hybrid compositions between such magmas and less fractionated compositions. Evidently the sampled ferrobasalts are close to the most evolved compositions that occur in any abundance on this portion of the East Pacific Rise.

Silicate mineralogy of basalts at DSDP Leg 54 Holes

Basalts drilled from the East Pacific Rise, OCP Ridge, and Siqueiros fracture zone during Leg 54 are texturally diverse. Dolerites are equigranular at Sites 422 and 428 and porphyritic, with phenocrysts of plagioclase (An69.73) and Ca-rich clinopyroxene (Ca42Mg48Fe10) at Site 427. The East Pacific Rise lavas and some of those from the OCP Ridge are fine-grained and porphyritic. The majority of the large crystals are clustered skeletal glomerocrysts of plagioclase An64-77), together with olivine (Fo80-87), Ca-rich clinopyroxene, or both. Euhedral phenocrysts of plagioclase, together with olivine, Carich clinopyroxene, and Cr-Al spinel in some cases, occur in most of the fine-grained lavas. These phenocrysts are small (maximum dimension <1 mm in all but one sample), sparse (combined modal amount <1% in all samples), and distinctive from the megacrysts which characterize many ocean-floor lavas. In two East Pacific Rise lavas, zoned plagioclase (An83 cores) is the sole phenocryst phase. In other porphyritic lavas from all the main East Pacific Rise and OCP Ridge units drilled during Leg 54, the plagioclase phenocrysts contain cores of bytownite (An79-87) surrounded by more-sodic feldspar (An67-77). Core/rim relationships vary from continuous normal zoning, through discontinuous zoning, to extensive resorption of the calcic cores in some samples. The compositions of the plagioclase calcic cores are systematically related to those of the glomerophyric plagioclase and olivine in the lavas containing them. Furthermore, only one compositional population of calcic cores occurs in each rock. The possible causes of these relationships are far from clear. Magma mixing, although superficially applicable, is inconsistent with important aspects of the phenocryst mineralogy of these particular lavas. A more satisfactory model to explain both phenocryst zoning and rapid glomerocryst growth immediately before extrusion may be constructed by postulating influx of water into the upwelling magmas within Layer 3 of the oceanic crust beneath the East Pacific Rise, and subsequent loss of part of this water during effervescence within feeder dykes between Layer 3 and the ocean floor. It is shown that this model is fully consistent with published data on water and carbon dioxide contents and ratios in the pillow-margin glasses, vesicles, and phenocryst inclusions of ocean-floor basalts. The evidence for the precipitation of plagioclase- dominated crystalline assemblages from these magmas in the upper part of Layer 3 is concordant with recent geophysically based modeling of the structure of the East Pacific Rise. Calcium-rich clinopyroxenes in dolerites from the OCP Ridge and Siqueiros fracture zone show radial, oscillatory, and sector-zoning. In Sample 428A-5-2 (Piece 5a), the compositional trends resulting from this zoning closely resemble those of the pyroxenes in some lunar lavas. The controls on crystallization of interstitial pigeonite - epitaxial upon augite - in this rock are discussed. Both sector-zoning of the augite and nucleation of pigeonite within microvolumes of magma with a low Ca(Mg + Fe) ratio appear to be important factors.

Geochemistry of ODP Hole 135-839B basalts

Experimental phase relations were used to assess the role of volatiles and crustal level fractional crystallization in the petrogenesis of lavas from Hole 839B in the central Lau Basin. Melting experiments were performed on Sample 135-839B-15R-2, 63-67 cm, at 1 atm, anhydrous, and 2 kbar, H2O-saturated (~6 wt% H2O in the melt) to determine the influence of variable pressure and H2O content on phase appearances, mineral chemistry, and liquid line of descent followed during crystallization. The effects of H2O are to depress the liquidus by ~100°C, and to suppress crystallization of plagioclase and orthopyroxene relative to olivine and high-Ca clinopyroxene. At 1 atm, anhydrous, olivine and plagioclase coexist near the liquidus, whereas orthopyroxene and then clinopyroxene appear with decreasing temperature. Crystallization of 50 wt% produces a residual liquid that is rich in FeO* (10.8 wt%) and poor in Al2O3 (13.6 wt%). At 2 kbar, H2O-saturated, the liquidus phases are olivine and chromian spinel, with high-Ca clinopyroxene appearing after ~10% crystallization. Plagioclase saturation is suppressed until ~20% crystallization has occurred. The residual liquid from 35 wt% crystallization is rich in AI2O3 (17.4 wt%), and poor in MgO (4.82 wt%); it contains moderate FeO* (8.2 wt%), and resembles the low-MgO andesites recovered from Hole 839B. On the basis of these experiments we conclude that the primitive lavas recovered from Hole 839B have experienced crystallization along the Ol + Cpx saturation boundary, under hydrous conditions (an ankaramitic liquid line of descent), and variable amounts of olivine and chromian spinel accumulation. The low-MgO andesites from Hole 839B are the products of hydrous fractional crystallization, at crustal pressures, of a parent magma similar to basaltic andesite Sample 135-839B-15R-2, 63-67 cm.

Chemiscal composition of basalts from DSDP Legs 69 and 70 Holes

Chemical compositions and 1-atm. phase relations were determined for basalts drilled from Holes 501, 504A, 504B, 505, and 505B on Legs 68, 69, and 70 of the Deep Sea Drilling Project. Chemical, experimental, and petrographic data indicate that these basalts are moderately evolved (Mg' values from 0.60 to 0.70), with olivine plus Plagioclase and often clinopyroxene on the liquidus. Chemical stratigraphy was used to infer that sequential influxes of magma into a differentiating magma chamber or separate flows from different magma chambers or both had occurred. Two major types of basalt were found to be inter layered: Group M, a rarely occurring type with major element chemistry and magmaphile element abundances within the range of the majority of ocean-floor basalts (TiO2 = 1.3%, Na2O 2.5%, Zr = 103 ppm, Nb = 2.5 ppm, and Y = 31 ppm); and Group D, a highly unusual series of basalt compositions that exhibit much lower magmaphile element abundances (TiO2 = 0.75-1.2%, Na2O = 1.7-2.3%, Zr = 34-60 ppm, Nb = 0.5-1.2 ppm, and Y = 16-27 ppm). The liquidus temperatures of the Group D basalts are high (1230- 1260°C) compared with those of other ocean-floor basalts of similar Mg' values. They have high CaO/Na2O ratios (5-8) and are calculated to be in equilibrium with unusually calcic Plagioclase (An78-84). The two basalt groups cannot be related by fractionation processes. However, constant Zr/Nb ratios (>40) for the two groups suggest a single mantle source, with differences in magmaphile element abundances and other element ratios (e.g., Zr/Ti, Zr/Y, Ce/Yb) arising through sequential melting of the same source. Magmas similar to Group D, if mixed with more typical mid-ocean-ridge basalt (MORB) magmas in shallow magma chambers, could provide a source for the highly calcic Plagioclase phenocrysts that appear in more common (i.e., less depleted) phyric ocean-floor basalts.

Petrology of basalts from DSDP Hole 83-504B

Basalts from Hole 504B, Leg 83, exhibit remarkable uniformity in major and trace element composition throughout the 1075.5 m of basement drilled. The majority of the basalts, Group D', have unusual compositions relative to normal (Type I) mid-ocean ridge basalts (MORB). These basalts have relatively high mg values (0.60-0.70) and CaO abundances (11.7-13.7%; Ca/Al = 0.78-0.89), but exhibit a marked depletion in compatible trace elements (Cr and Ni); moderately incompatible trace elements (Zr, Y, Ti, etc.); and highly incompatible trace elements (Nb, LREE, etc.). Petrographic and compositional data indicate that most of these basalts are evolved, having fractionated significant amounts of plagioclase, olivine, and clinopyroxene. Melting experiments on similar basalt compositions from the upper portion of Hole 504B (Leg 70; Autio and Rhodes, 1983) indicate that the basalts are co-saturated with olivine and plagioclase and often clinopyroxene on the 1-atm. liquidus. Two rarely occurring groups, M' and T, are compositionally distinct from Group D' basalts. Group T is strongly depleted in all magmaphile elements except the highly incompatible ones (Nb, La, etc.), while Group M' has moderate concentrations of both moderately and highly incompatible trace elements and is similar to Type I MORB. Groups M' and T cannot be related to Group D' nor to each other by crystal fractionation, crystal accumulation, or magma mixing. The large differences in magmaphile element ratios (Zr/Nb, La/Yb) among these three chemical groups may be accounted for by complex melting models and/or local heterogeneity of the mantle beneath the Costa Rica Ridge. Xenocrysts and xenoliths of plagioclase and clinopyroxene similar in texture and mineral composition to crystals in coarse-grained basalts from the lower portion of the hole are common in Hole 504B basalts. These suggest that addition of solid components either from conduit or magma chamber walls has occurred and may be a common source of disequilibrium crystals in these basalts. However, mixing of plagioclase-laden depleted melts (similar to the Costa Rica Ridge Zone basalts) with normal MORB magmas could provide an alternate source for some refractory plagioclase crystals found out of equilibrium in many phyric MORB. The uniformity of major element compositions in Hole 504B basalts affords an ideal situation for investigating the effects of alteration on some major and trace elements in oceanic basalts. Alteration observed in whole-rock samples records primarily two events - a high-temperature and a low-temperature phase. High-temperature phases include: chlorite, talc, albite, actinolite, sphene, quartz, and pyrite. The low-temperature phases include smectite (saponite), epistilbite or laumontite, and minor calcite. Laumontite may actually straddle the gap between the low- and high-temperature mineral assemblages. Alteration is restricted primarily to partial replacement of primary phases. Metamorphic grade, in general, increases from the top to the bottom of Hole 504B (Legs 69, 70, and 83) as seen in the change from a smectiteto- chlorite-dominated secondary mineral assemblage. However, a systematic progression for the interval recovered during Leg 83 is not apparent. Rather, the extent of alteration appears to be a function of the initial texture and fracture density. Variations in whole-rock major and trace element concentrations cannot be attributed convincingly to any differences in alteration observed. Compositional characteristics of the secondary minerals indicated that extensive remobilization of elements has not occurred; local redistribution is suggested in most cases. Thus, the major and trace element signature of these basalts remains effectively the same as the original composition prior to alteration.

Estimation of cooling of lavas from Serocki volcano

A dynamic crystallization study was undertaken to provide a framework for linking the textural variations observed in the Hole 648B lavas with the size and morphology of cooling units inferred from drilling and submersible observation. The textures produced in cooling rate experiments carried out using a Serocki lava (ALV-1690-20) are comparable to the groundmass textural characteristics of lavas from Serocki volcano. The results of the dynamic crystallization study provide a quantitative link between texture, cooling rate, and eruption temperature. The maximum half-width of cooling units estimated from textural characteristics is on the order of 3 m, a value consistent with constraints from drilling and submersible observation. Textural characteristics indicate that the temperature from which cooling began was slightly above the liquidus. The relation between cooling rate and texture are also tested on a drill core sample of basalt of similar composition from a 9-m-thick flow in DSDP Hole 396B.

Geochemistry and isotopic ratios of Neogene basalts from Spitzbergen Island, Svalbard archipelago

Petrological and geochemical data obtained on Neogene magmatism restricted to a deep fault in Andree Land at Spitsbergen Island, which was related to the overall restyling of the Arctic territory at 25-20 Ma, indicate that the derivation of the Neogene magmas was significantly affected by the continental pyroxenite mantle. The Neogene basalts are noted for a radiogenic isotopic composition of Pb (207Pb/204Pb= 15.5-15.55, 206Pb/204Pb = 18.4-18.6, 208Pb/204Pb = 38.4-38.6) and Sr (87Sr/86Sr = 0.7038-0.7048) at low 143Nd/144Nd = 0.5129. Melts of this type are the extremely enriched end member of the isotopic mixing of a depleted and enriched sources and determine a geochemical trend that passes through the compositions of alkaline magmas from Quaternary volcanoes at Spitsbergen and weakly enriched tholeiites of the Knipovich Ridge, which started to develop simultaneously with the onset of Neogene magmatism in the western part of Spitsbergen. The composition of the liquidus olivine (which is rich in NiO) indicates that melting occurred in the olivine-free mantle. Our data thus testify that a significant role in the genesis of the Neogene magmas was played by continental pyroxenite mantle.