Geochemistry and petrology of dredged basalts from the Bouvet triple junction,South Atlantic

Basalts dredged from the Bouvet triple junction (South Atlantic), from the Mid-Atlantic Ridge near the triple junction, and from a spreading center east of Bouvet Island differ from normal mid-ocean ridge tholeiites by having higher concentrations of K and other large-ion-lithophile elements, higher ${}^{87}\text{Sr}\text{:}{}^{86}\text{Sr}$ ratios, and rare earth element distributions which show relative enrichment in the lighter rare earths. The basalts are more fractionated than typical oceanic tholeiites, however, fractional crystallization does not fully account for their chemical characteristics, and it appears that they were derived from special source materials, contaminated perhaps by a mantle plume rising beneath Bouvet Island.     

Magmatic and hydrothermal processes in the Bouvet Triple Junction Region (South Atlantic)

Results of electron microprobe and microthermometric studies of samples collected from the Bouvet Triple Junction Region (BTJR) during a joint Russian-Italian geological expedition on the R/V Academician Nikolaj Strakhov (1994) have revealed new data on the composition of basaltic magmas and oceanic hydrothermal fluids connected with magmatic processes. Detailed analysis of basaltic glasses shows that the modem Mid-Atlantic Ridge (MAR) rift valley is composed of normal mid-ocean ridge basalts with low concentrations of K₂ O and TiO_z (N-MORB), while its flanks are more enriched with these components approaching E-MORB. A marked influence of the Bouvet hot spot volcanism on magma generation on the South-West Indian Ridge (SWIR) near Bouvet Island is observed. Basaltic melts in this area belong to alkalic and transitional series and have maximum contents of K₂O, TiO₂, H₂O.
Microthermometric analyses of fluid inclusions in the samples from the BTJR have revealed major differences in the oceanic hydrothermal fluid systems on the MAR and near SWIR, which depends on the peculiarities of magma. In the area of the MAR (with dry melts) only H₂O solution inclusions in quartz were found; thus, seawater is probably the only primary source of hydrothermal fluids (NaCl + MgCl₂+ H₂O; T = 170–200°C). In the SWIR area (with the high content of water in melts) syngenetic liquid CO₂ and H₂O solution inclusions in quartz indicate the influence of the magmatic fluid component on the ore-forming water/carbon dioxide solutions (NaCl + CaC1₂+ H₂O + CO₂; T = 200–310 °C; P = 900–1700 bar).     

A microearthquake survey of Bouvet Island, South Atlantic

A microearthquake survey carried out during the 1978–1979 Norwegian Antarctic Research Expedition indicates that only minor seismic activity is associated with the Bouvet volcano.     

Mantle peridotites from the Bouvet Triple Junction Region, South Atlantic

ABSTRACT The Bouvet Triple Junction (BTJ) region in the South Atlantic, where the African, South American and Antarctica plates meet, is affected by several topographic/melting anomalies. Causes of these anomalies were investigated through a study of mantle-derived serpentinized peridotites sampled from three sites in the BTJ region: (1) the Inner Corner High at the intersection of the America Antarctic Ridge (AAR) with the Conrad transform; (2) the south wall of the Bouvet transform (South West Indian Ridge, SWIR); and (3) the eastern Bouvet SWIR Transform Intersection. The degree of melting undergone by these rocks was estimated from relic mineral major- and trace-element composition. Geochemical profiles from residual peridotites and associated basalts show a > 1000-km-wide melting anomaly centred on the Bouvet and Spiess topographic anomalies.     

Platinum-group element systematics in Mid-Oceanic Ridge basaltic glasses from the Pacific, Atlantic, and Indian Oceans

The concentrations of Ir, Ru, Pt and Pd have been determined in 29 Mid-Oceanic Ridge basaltic (MORB) glasses from the Pacific (N = 7), the Atlantic (N = 10) and the Indian (N = 11) oceanic ridges and the Red Sea (N = 1) spreading centers. The effect of sulfide segregation during magmatic differentiation has been discussed with sample suites deriving from parental melts produced by high (16%) and low (6%) degrees of partial melting, respectively. Both sample suites define positive and distinct covariation trends in platinum-group elements (PGE) vs. Ni binary plots. The high-degree melting suite displays, for a given Ni content, systematically higher PGE contents relative to the low-degree melting suite. The mass fraction of sulfide segregated during crystallization (X_sulf), the achievement of equilibrium between sulfide melt and silicate melts (R_eff), and the respective proportions between fractional and batch crystallization processes (S_b) are key parameters for modeling the PGE partitioning behavior during S-saturated MORB differentiation. Regardless of the model chosen, similar sulfide melt/silicate melt partition coefficients for Ir, Ru, Pt and Pd are needed to model the sulfide segregation process, in agreement with experimental data. When corrected for the effect of magmatic differentiation, the PGE data display coherent variations with partial melting degrees. Iridium, Ru and Pt are found to be compatible in nonsulfide minerals whereas the Pd behaves as a purely chalcophile element. The calculated partition coefficients between mantle sulfides and silicate melts (assuming a PGE concentration in the oceanic mantle at ∼0.007 × CI-chondritic abundances) increase from Pd (∼10³) to Ir (∼10⁵). This contrasting behavior of PGE during S-saturated magmatic differentiation and mantle melting processes can be accounted for by assuming that Monosufide Solid Solution (Mss) controls the PGE budget in MORB melting residues whereas MORB differentiation processes involve Cu-Ni-rich sulfide melt segregation.     

Alteration of basaltic glass: Mechanisms and significance for the oceanic crust-seawater budget

Alteration of basaltic glass to palagonite is characterized by a nearly isomolar exchange of SiO₂, Al₂O₃, MnO, MgO, CaO, Na₂O, P₂O₅, Zn, Cu, Ni, Cr, Hf, Sc, Co and REE for H₂O and K₂O, whilst TiO₂ and FeO are passively accumulated during removal of the remaining cations. The network forming cations Al and Si are removed from the glass in proportion to the gain in Ti and Fe, whilst the other cations do not show a significant relationship to the amount of Ti and Fe accumulation. Sr isotopic data show that during palagonite formation approximately 85% of the basaltic Sr is lost to the hydrous solutions and 40% of seawater Sr is added to the glass, yielding an average loss of the same order of magnitude as of the network forming cations. Losses and gains of oxides yield an average increase of +105% TiO₂.K, Rb, and Cs show high increases, but $\text{K}\text{Rb}$ and $\text{K}\text{Cs}$ ratios indicate two different alteration processes: (1) formation of palagonite involves a drastic decrease in these ratios, indicating structural similarities between palagonite and smectite; (2) surface alteration of glass is characterized by an increase in $\text{K}\text{Rb}$ and $\text{K}\text{Cs}$ ratios, probably best interpreted as sorption of alkalies in ratios approximating those of seawater.The total fluxes involved in alteration of glass in the upper portion of the oceanic crust are estimated from the modal abundance of palagonite in the oceanic crust and the abundance of the vein materials smectite and carbonate. Smectite and carbonates act as a sink for a significant portion of the elements liberated up during alteration of basaltic glass except for Na and Al, which are probably taken up by zeolites and/or albite, possibly hidden in the macroscopic estimate of carbonate. Formation of the observed quantity of secondary phases requires additional sources for Si, Fe. Ca and K. K is provided in excess from the inflowing seawater at reasonable water/rock ratios. The remaining excess Ca, Si and Fe required may be derived by alteration of interstitial glass and breakdown of anorthite rich plagioclase and titano-magnetite, and/or by supply of deeper seated metamorphic reactions.     

大青山地区中生代玄武质火山岩岩石地球化学特征

对满洲里地区大青山盆地中生代玄武质火山岩类地球化学特征进行讨论,结合野外观察和前人资料,对其岩浆演化、成因及成岩构造环境进行探讨,为下一步工作提供依据。分析可知,该区玄武质火山岩类岩浆源于富集不相容元素的富集地幔,后有壳源物质参与,是岩石圈伸展背景下早期流体交代岩石圈地幔发生部分熔融的产物。通过火山岩地球化学特征分析以及和邻区产铀火山岩特征类比可知,本区具备较好的火山热液型铀及多金属成矿的构造环境及火山岩浆演化系列。     

The morphostructure of the South Atlantic Ridge in the Tristan da Cunha hot spot area

Investigation of the rift zone and flanks of the South Atlantic midoceanic ridge in the Tristan da Cunha hot spot area revealed that their morphostructure is atypical of slow spreading ridges. Feeding the spreading center with magmatic material, the hot spot changes the morphology of the axial zone and transform faults. It itself forms a relief ensemble that differs from the rift one as well. The continuous migration of the spreading center in the westerly direction stimulates the formation of a spacious volcanic highland, which is responsible for the regional asymmetry of ridge flanks in its extended segments (hundreds kilometers long).     

Organic matter provenance,palaeoproductivity and bottom water anoxia during the Cenomanian/Turonian oceanic anoxic event in the Newfoundland Basin (northern proto North Atlantic Ocean)

Free and sulfur-bound biomarkers in sediments deposited in the northern proto North Atlantic (Newfoundland Basin, ODP Site 1276) during the Cenomanian–Turonian oceanic anoxic event 2 (OAE-2) were studied. The δ¹³C records of phytane and lycopane confirmed the stratigraphic position of the positive carbon isotope excursion associated with OAE-2, previously reported for total organic carbon (TOC) and β,β-homohopane. Sediments before and after the OAE-2 interval were poor in organic matter (OM) and comprised numerous gravity flow deposits. The interval itself was composed of pelagic sediments with occasionally a much higher TOC content of up to 12.7%. The OAE-2 sediments were characterized by a low amount of terrestrial OM since the dominant biological sources of the biomarkers were aquatic in origin. High hopane, pentamethylicosane (PMI), and squalane abundances in the OM-rich sediments pointed to a relatively high input of prokaryotes, partly derived from cyanobacteria, as suggested by the occasional occurrence of 2-methylhopanes. PMI comprised both the regular and irregular isomer and changes in the δ¹³C of PMI are thought to reflect contributions from methanogenic and methanotrophic archea. The high relative concentration of lycopane indicated that bottom water conditions were anoxic during large parts of the OAE-2 interval. In one horizon, trace amounts of isorenieratane provided evidence for the occasional occurrence of photic zone anoxia. Taken together, the data imply that oceanic anoxia, and probably also high productivity, reached the northernmost part of the proto-North Atlantic during OAE-2, albeit that photic zone anoxia was much less common than in the southern proto-North Atlantic.     

南大西洋渐新世初碳酸盐记录(ODP 1263站)

渐新世初期,南极大陆在短时间内出现永久性冰盖,地球由两极无冰进入到单极有冰的特殊时期。越来越多的研究表明,这一重大气候转型事件与大气CO2及大洋碳储库的变化密切相关。南大西洋ODP 1263站碳酸钙软泥的粒度分析揭示了在渐新世初期发生的强烈碳酸盐溶解事件,碳酸盐溶解超前于底栖有孔虫氧同位素重值约100 ka,显示碳酸盐溶解事件先于南极冰盖的形成。由于碳酸钙泵的作用,碳酸盐的溶解会消耗大量的大气CO2,从而可能驱动了气候的快速变冷,导致南极大陆永久性冰盖发育。     

Seismic anisotropy in the region of the Chile margin triple junction

We have measured shear wave splitting at three temporary three-component short period stations that were deployed in southern Chile above the subducted Chile Rise spreading centre (Taitao Peninsula and environs). Subduction of the Chile Rise has been occurring beneath South America for at least the past 14 m.y. Previously published models of the ridge subduction posit the existence of ‘slab windows’, asthenosphere-filled gaps between subducted lithosphere segments of the spreading ridge, through which mantle might flow. Our preliminary results include two consistent fast polarization directions of splitting in the study region. Delay times between fast and slow split shear waves average around 1.0 s for all phases (ScS, PcS, SKS, and SKKS) that we measured. Fast-axis azimuths vary systematically among the three stations: near the coast, fast axes are parallel to the spreading ridge segments of the Chile Rise (approximately N-trending). This splitting fast-axis direction probably reflects either along-axis asthenospheric flow or results from the preferential attenuation effects of aligned pockets of melt at the subducted ridge segment. At one inland station above the slab window, we find two splitting fast-axis directions, one parallel to the subducted Chile Rise ridge segments, and a second trending NW–SE. We infer that upper mantle deformation in the vicinity of a well developed slab window is complicated and probably involves two superposed directions of upper mantle deformation. One of these directions (NW–SE) may indicate anomalous flow of asthenospheric mantle in the vicinity of the slab window gap.     

Late Cenozoic transpressional ductile deformation north of the Nazca–South America–Antarctica triple junction

The southern Andes plate boundary zone records a protracted history of bulk transpressional deformation during the Cenozoic, which has been causally related to either oblique subduction or ridge collision. However, few structural and chronological studies of regional deformation are available to support one hypothesis or the other. We address along- and across-strike variations in the nature and timing of plate boundary deformation to better understand the Cenozoic tectonics of the southern Andes.Two east–west structural transects were mapped at Puyuhuapi and Aysén, immediately north of the Nazca–South America–Antarctica triple junction. At Puyuhuapi (44°S), north–south striking, high-angle contractional and strike-slip ductile shear zones developed from plutons coexist with moderately dipping dextral-oblique shear zones in the wallrocks. In Aysén (45–46°), top to the southwest, oblique thrusting predominates to the west of the Cenozoic magmatic arc, whereas dextral strike-slip shear zones develop within it.New ⁴⁰Ar–³⁹Ar data from mylonites and undeformed rocks from the two transects suggest that dextral strike-slip, oblique-slip and contractional deformation occurred at nearly the same time but within different structural domains along and across the orogen. Similar ages were obtained on both high strain pelitic schists with dextral strike-slip kinematics (4.4±0.3 Ma, laser on muscovite–biotite aggregates, Aysén transect, 45°S) and on mylonitic plutonic rocks with contractional deformation (3.8±0.2 to 4.2±0.2 Ma, fine-grained, recrystallized biotite, Puyuhuapi transect). Oblique-slip, dextral reverse kinematics of uncertain age is documented at the Canal Costa shear zone (45°S) and at the Queulat shear zone at 44°S. Published dates for the undeformed protholiths suggest both shear zones are likely Late Miocene or Pliocene, coeval with contractional and strike-slip shear zones farther north. Coeval strike-slip, oblique-slip and contractional deformation on ductile shear zones of the southern Andes suggest different degrees of along- and across-strike deformation partitioning of bulk transpressional deformation.The long-term dextral transpressional regime appears to be driven by oblique subduction. The short-term deformation is in turn controlled by ridge collision from 6 Ma to present day. This is indicated by most deformation ages and by a southward increase in the contractional component of deformation. Oblique-slip to contractional shear zones at both western and eastern margins of the Miocene belt of the Patagonian batholith define a large-scale pop-up structure by which deeper levels of the crust have been differentially exhumed since the Pliocene at a rate in excess of 1.7 mm/year.     

Effect of boron on the water speciation in (alumino)silicate melts and glasses

The investigation of hydrous boro(alumino)silicate melts and glasses with near infrared (NIR) spectroscopy revealed an important effect of boron on the water speciation. In the NIR spectra of B-bearing glasses new hydroxyl-related bands develop at the high frequency side of the 4500 cm⁻¹ peak. In NaAlSi₃O₈ + B₂O₃ glasses this new peak is present as a shoulder at 4650 cm⁻¹, and in NaAlSi₃O₈-NaBSi₃O₈ (Ab-Rd) glasses it appears as a resolved peak at 4710 cm⁻¹. These bands increase with increasing boron concentration, suggesting that they are due to B-OH complexes. Furthermore, the variations in the NIR spectra indicate that with increasing B-content, but constant total water concentration, the amount of structurally bonded hydroxyl groups increases at the expense of molecular H₂O. For example, at a total water concentration of 4 wt.%, pure Rd-glass contains ∼50% more water as hydroxyl groups than pure Ab-glass.In-situ NIR spectroscopy at high P and T using a hydrothermal diamond-anvil cell was used to gain information about the temperature dependence of the water speciation in NaBSi₃O₈ melts. The data demonstrate the conversion of molecular H₂O to hydroxyl groups with increasing temperature. However, a fully quantitative evaluation of the high T spectra was hampered by problems with defining the correct baseline in the spectra. As an alternative approach annealing experiments on a Rd-glass containing 2.8 wt.% water were performed. The results confirm the conversion of H₂O to OH groups with increasing T, but also suggest that the OH groups represented by the 4710 cm⁻¹ peak (B-OH) participate much less in the conversion reaction compared to X-OH, represented by the 4500 cm⁻¹ peak.     

Bursts of seismicity near the Cocos-North American-Caribbean triple junction

Three previously proposed long-term premonitory patterns, pattern Sigma, pattern Swarms, and ‘bursts of aftershocks’, appear to be moderately successfull for large (M 7.3) earthquakes which have occurred in the vicinity of the North American-Caribbean-Cocos triple junction between 1930 and July 1980.     

Origin of basaltic magmas in the Mojave Desert area,California

The basaltic lavas erupted throughout the Mojave Desert are basanites (SiO₂<46%, normative nepheline>5%, and K₂O>1.5%), alkali-olivine basalts (SiO₂=46–48%; ne=0–5%; and K₂O=1.0–1.5%), and low-alumina, sub-alkaline basalts (SiO₂=48–51%; ne=0; K₂O<1.0%). One volcano, Pisgah Crater, erupted five times, with lava from each successive phase containing more silica and less potash than the one proceeding it. This compositional trend is the reverse of that expected from differentiation of a single alkalic magma, and therefore, may represent a succession of magmas tapped from a zone of continuing partial melting in the mantle.These lava compositions suggest that first melting was under high water pressure and was followed by relatively dry partial melting of gamet-orthopyroxene-clinopyroxene-olivine assemblages. The successive increase in silica and alkali decrease also requires that the partial melting zone move to shallower levels.All lavas sampled in the Mojave Desert area have compositions that can best be explained by the extraction of magma from such a rising melting zone, analogous to the mantle diapirs suggested by Green and Ringwood.