Strontium and oxygen isotopic systems in waters of mud volcanoes of the Taman Peninsula

Ten of eleven analyzed water samples from mud volcanoes of the Taman Peninsula are characterized by ⁸⁷Sr/⁸⁶Sr ratio within 0.70734–0.70957, which overlaps the values typical of the Mesozoic and Cenozoic sedimentary carbonates, but sharply differs from the value in the clayey sediments of the Maikop Group (0.7157 ± 0.0022). These data indicate that the strontium isotopic composition is mainly defined by carbonate reservoirs, with relatively little effect of elision solutions, input of which is noticeable only in the water of Gladkovsky Volcano (⁸⁷Sr/⁸⁶Sr = 0.71076). The high δ¹⁸O in mud volcanic waters (up to 14.2‰) can also be attributed to ionic exchange with sedimentary carbonates at temperatures around 150°C.     

Isotopic composition of oxygen and hydrogen in mud-volcanic waters from Taman (Russia) and Kakhetia (Eastern Georgia)

The ¹⁸O and D values in mud-volcanic waters of the Taman Peninsula and Kakhetia vary from +0.7 to +10.0 and from –37 to –13 , respectively. These values increase as the Greater Caucasus is approached. The increase in 18O and D also positively correlates with fluid generation temperatures based on hydrochemical geothermometers. This is accompanied by changes in the chemical composition of waters, in which contents of alkali metals, HCO^– ₃ ion, and boron increase, while the content of halogen ions (Cl, Br, J) decreases. Changes in the isotopic composition of water are also accompanied by the increase of ¹³ in methane and decrease of ¹¹ B in clays. Analysis of formal models of the evolution of isotopic composition of mud-volcanic waters showed that mud volcanoes are recharged by freshened water from the Maikop paleobasin with an inferred isotopic composition of D –40 and ¹⁸ O –6. Based on this assumption, the ¹⁸O and D values observed in mud-volcanic waters can be explained not only by processes of distillation and condensation in a closed system, but also by combined processes of isotopic reequilibration in the water-illite-methane system.Translated from Litologiya i Poleznye Iskopaemye, No. 2, 2005, pp. 143–158.Original Russian Text Copyright © 2005 by Lavrushin, Dubinina, Avdeenko.     

Isotopic evidence (Sr/Sr, δLi) for alteration of the oceanic crust at deep-rooted mud volcanoes in the Gulf of Cadiz, NE Atlantic Ocean

The chemical and isotopic composition of pore fluids is presented for five deep-rooted mud volcanoes aligned on a transect across the Gulf of Cadiz continental margin at water depths between 350 and 3860 m. Generally decreasing interstitial Li concentrations and ⁸⁷Sr/⁸⁶Sr ratios with increasing distance from shore are attributed to systematically changing fluid sources across the continental margin. Although highest Li concentrations at the near-shore mud volcanoes coincide with high salinities derived from dissolution of halite and late-stage evaporites, clayey, terrigenous sediments are identified as the ultimate Li source to all pore fluids investigated. Light δ⁷Li values, partly close to those of hydrothermal vent fluids (δ⁷Li: +11.9‰), indicate that Li has been mobilized during high-temperature fluid/sediment or fluid/rock interactions in the deep sub-surface. Intense leaching of terrigenous clay has led to radiogenic ⁸⁷Sr/⁸⁶Sr ratios (0.7106) in pore fluids of the near-shore mud volcanoes. In contrast, non-radiogenic ⁸⁷Sr/⁸⁶Sr ratios (0.7075) at the distal locations are attributed to admixing of a basement-derived fluid component, carrying an isotopic signature from interaction with the basaltic crust. This inference is substantiated by temperature constraints from Li isotope equilibrium calculations suggesting exchange processes at particularly high temperatures (>200 °C) for the least radiogenic pore fluids of the most distal location.Advective pore fluids in the off-shore reaches of the Gulf of Cadiz are influenced by successive exchange processes with both oceanic crust and terrigenous, fine-grained sediments, resulting in a chemical and isotopic signature similar to that of fluids in near-shore ridge flank hydrothermal systems. This suggests that deep-rooted mud volcanoes in the Gulf of Cadiz represent a fluid pathway intermediate between mid-ocean ridge hydrothermal vent and shallow, marginal cold seep. Due to the thicker sediment coverage and slower fluid advection rates, the overall geochemical signature is shifted towards the sediment-diagenetic signal compared to ridge flank hydrothermal environments.     

Formation of Mud-Volcanic Fluids in Taman (Russia) and Kakhetia (Georgia): Evidence from Boron Isotopes

Temperatures of the formation of mud-volcanic waters are determined based on concentrations of some temperature-dependent components (Na–Li, Mg–Li). Estimates obtained for the Taman and Kakhetia regions are similar and range from 45 to 170°, which correspond to depths of 1–4.5 km. The calculated temperatures correlate with the chemical (Li, Rb, Cs, Sr, Ba, B, I, and HCO₃) composition of water and ¹³ (₂) and ¹³ (CH₄) values in spontaneous gases. The isotope values indicate that mechanisms of the formation of ¹³-rich gases, i.e., gases with high ¹³ values (up to +16.0 in ₂ and –23.4 in CH₄) in mud-volcanic systems of Taman and Kakhetia are governed by fluid-generation temperatures rather than the supply of abyssal gases. The ¹¹ value was determined for the first time in mud-volcanic products of the Caucasus region. This value ranges from +22.5 to +39.4 in the volcanic water of Georgia, from –1.2 to +7.4 in the clayey pulp of Georgia, and from –7.6 to +13.2 in the clayey pulp of Taman. It is shown that the ¹¹ value in clay correlates with the fluid-generation temperature and ¹¹ correlates with ¹³ in carbon-bearing gases. These correlations probably testify to the formation of different phases of mud-volcanic emanations in a single geochemical system and suggest the crucial role of temperature in the development of isotope-geochemical features.     

Geochemistry of mud volcano fluids in the Taiwan accretionary prism

Taiwan is located at the collision boundary between the Philippine Sea Plate and the Asian Continental Plate and is one of the most active orogenic belts in the world. Fluids sampled from 9 sub-aerial mud volcanoes distributed along two major geological structures in southwestern Taiwan, the Chishan fault and the Gutingkeng anticline, were analyzed to evaluate possible sources of water and the degree of fluid-sediment interaction at depth in an accretionary prism. Overall, the Taiwanese mud volcano fluids are characterized by high Cl contents, up to 347 mM, suggesting a marine origin from actively de-watering sedimentary pore waters along major structures on land. The fluids obtained from the Gutingkeng anticline, as well as from the Coastal Plain area, show high Cl, Na, K, Ca, Mg and NH₄, but low SO₄ and B concentrations. In contrast, the Chishan fault fluids are much less saline (1/4 seawater value), but show much heavier O isotope compositions (δ¹⁸O=5.1–6.5 ‰). A simplified scenario of mixing between sedimentary pore fluids and waters affected by clay dehydration released at depth can explain several crucial observations including heavy O isotopes, radiogenic Sr contents (⁸⁷Sr/⁸⁶Sr=0.71136–0.71283), and relatively low salinities in the Chishan fluids. Gases isolated from the mud volcanoes are predominantly CH₄ and CO₂, where the CH₄–C isotopic compositions show a thermogenic component of δ¹³C=−38 ‰. These results demonstrate that active mud volcano de-watering in Taiwan is a direct product of intense sediment accretion and plate collision in the region.     

Isotope and chemical composition of gases from mud volcanoes in the Taman Peninsula and problem of their genesis

Variations in the carbon isotope composition in gases and waters of mud volcanoes in the Taman Peninsula are studied. The δ¹³C values in CH₄ and CO₂ vary from ?59.5 to ?44.0‰ (δ¹³C_av = ?52.4 ± 5.4‰) and from ?17.8 to +22.8‰ (δ¹³C_av = +6.9 ± 9.3‰), respectively. In waters from most mud volcanoes of the peninsula, this parameter ranges from +3.3 to +33.1‰, although locally lower values are also recorded (up to ?12‰. Fractionation of carbon isotopes in the CO₂-HCO₃ system corresponds to the isotope equilibrium under Earth’s surface temperatures. The growth of carbon dioxide concentration in the gaseous phase and increase in the HCO₃ ion concentration in their water phase is accompanied by the enrichment of the latter with the heavy ¹³C isotope. The δ¹³C_TDIC value in the water-soluble carbon depends on the occurrence time of water on the Earth’s surface (exchange with atmospheric CO₂, methane oxidation, precipitation of carbonates, and other processes), in addition to its primary composition. In this connection, fluctuations in δ¹³C_TDIC values in mud volcanoes with stagnant waters may amount to 10–20‰. In the clayey pulp, concentrations of carbonate matter recalculated to CaCO₃ varies from 1–4 to 36–50 wt %. The δ¹³C value in the latter ranges from ?3.6 to +8.4‰. Carbonate matter of the clayey pulp represents a mixture of sedimentogenic and authigenic carbonates. Therefore, it is usually unbalanced in terms of the carbon isotope composition with the water-soluble CO₂ forms.     

Isotope and trace element evidence for three component mixing in the genesis of the North Luzon arc lavas (Philippines)

Post-3Ma volcanics from the N Luzon arc exhibit systematic variations in ⁸⁷Sr/⁸⁶Sr (0.70327–0.70610), ¹⁴³Nd/¹⁴⁴Nd (0.51302–0.51229) and ²⁰⁸Pb^*/²⁰⁶Pb^* (0.981–1.035) along the arc over a distance of about 500 km. Sediments from the South China Sea west of the Manila Trench also exhibit striking latitudinal variations in radiogenic isotope ratios, and much of the isotopic range in the volcanics is attributed to variations in the sediment added to the mantle wedge during subduction. However, Pb-Pb isotope plots reveal that prior to subduction, the mantle end-member had high 8/4, and to a lesser extent high 7/4, similar to that in MORB from the Indian Ocean and the Philippine Sea Plate. Th isotope data on selected Holocene lavas indicate a source with unusually high Th/U ratios (4.5–5.5). Combined trace element and isotope data require that three end-members were implicated in the genesis of the N Luzon lavas: (1) a mantle wedge end-member with a Dupal-type Pb isotope signature, (2) a high LIL/HFS subduction component interpreted to be a slab-derived hydrous fluid, and (3) an isotopically enriched end-member which reflects bulk addition (<5%) of subducted S China Sea terrigenous sediment. The ⁸⁷Sr/⁸⁶Sr ratios in the volcanics show a restricted range compared with that in the sediments, and this contrasts with ¹⁴³Nd/¹⁴⁴Nd and ²⁰⁸Pb^*/²⁰⁶Pb^*, both of which have similar ranges in the volcanics and sediments. Such differences imply that whereas the isotope ratios of Nd, Pb and Th are dominated by the component from subducted sediment, those of Sr reflect a larger relative contribution from the slab-derived fluid.     

Isotope geochemistry of the Tieluping silver-lead deposit, Henan, China: A case study of orogenic silver-dominated deposits and related tectonic setting

The Tieluping silver deposit, which is sited along NE-trending faults within the high-grade metamorphic basement of the Xionger Terrane in the Qinling orogenic belt, is part of an important, recently discovered Mesozoic orogenic-type Ag-Pb belt. Ore formation includes three stages: an early barren quartz-pyrite stage (E), an intermediate polymetallic sulfide ore stage (M), and a late barren carbonate stage (L). Carbon, sulfur and lead isotope systematics indicate that the E-stage fluids are deeply sourced; the L-stage fluids are shallow-sourced meteoric water; whereas the M-stage fluids are a mix of deep-sourced and shallow-sourced fluids. Sulfur and lead isotope data show that the ore-forming fluids must have originated from a source with elevated radiogenic lead and low ³⁴S values, that differs significantly from exposed geologic units in the Xionger Terrane, the lower crust and the mantle. This supports the view that the carbonate-shale-chert sequences of the Guandaokou and Luanchuan Groups south of the Machaoying fault might be the favorable sources, although little is known about their isotopic compositions. A tectonic model that combines collisional orogeny, metallogeny and hydrothermal fluid flow is proposed to explain the formation of the Tieluping silver deposit. During the Mesozoic collision between the North China Craton and South China Block (Early-Mid Triassic Indosinian Orogeny), crustal slabs containing the carbonate-shale-chert sequences of the Guandaokou and Luanchuan Groups, locally rich in organic matter (carbonaceous shale), were thrust northwards beneath the Xionger Terrane along the Machaoying fault. Metamorphic devolatilisation of this underthrust slab probably provided the ore-forming fluids to develop the Ag-Pb ore belt, which includes the Tieluping silver deposit. Fluids and magmas were emplaced during extensional stages related to the Jurassic-Cretaceous Yanshanian Orogeny.Editorial Handling: B. Lehmann     

Microbial methane turnover at mud volcanoes of the Gulf of Cadiz

The Gulf of Cadiz is a tectonically active area of the European continental margin and characterised by a high abundance of mud volcanoes, diapirs, pockmarks and carbonate chimneys. During the R/V SONNE expedition “GAP-Gibraltar Arc Processes (SO-175)” in December 2003, several mud volcanoes were surveyed for gas seepage and associated microbial methane turnover. Pore water analyses and methane oxidation measurements on sediment cores recovered from the centres of the mud volcanoes Captain Arutyunov, Bonjardim, Ginsburg, Gemini and a newly discovered, mud volcano-like structure called “No Name” show that thermogenic methane and associated higher hydrocarbons rising from deeper sediment strata are completely consumed within the seabed. The presence of a distinct sulphate-methane transition zone (SMT) overlapping with high sulphide concentrations suggests that methane oxidation is mediated under anaerobic conditions with sulphate as the electron acceptor. Anaerobic oxidation of methane (AOM) and sulphate reduction (SR) rates show maxima at the SMT, which was found between 20 and 200 cm below seafloor at the different mud volcanoes. In comparison to other methane seeps, AOM activity (<383 mmol m⁻² year⁻¹) and diffusive methane fluxes (<321 mmol m⁻² year⁻¹) in mud volcano sediments of the Gulf of Cadiz are low to mid range. Corresponding lipid biomarker and 16S rDNA clone library analysis give evidence that AOM is mediated by a mixed community of anaerobic methanotrophic archaea and associated sulphate reducing bacteria (SRB) in the studied mud volcanoes. Little is known about the variability of methane fluxes in this environment. Carbonate crusts littering the seafloor of mud volcanoes in the northern part of the Gulf of Cadiz had strongly ¹³C-depleted lipid signatures indicative of higher seepage activities in the past. However, actual seafloor video observations showed only scarce traces of methane seepage and associated biological processes at the seafloor. No active fluid or free gas escape to the hydrosphere was observed visually at any of the surveyed mud volcanoes, and biogeochemical measurements indicate a complete methane consumption in the seafloor. Our observations suggest that the emission of methane to the hydrosphere from the mud volcano structures studied here may be insignificant at present.     

Fluid venting activity on the Costa Rica margin: new results from authigenic carbonates

Carbonate precipitates on mounds and along tectonic scarps off the Costa Rica margin are manifestations of subduction-induced dewatering. The long-term dewatering history is recorded in mineralogical, petrological and isotope signals of carbonates recovered from these sites. The carbonates are strongly depleted in ¹³C (–11 to –53 PDB) and enriched in ¹⁸O (+4 to +8 PDB). Thermogenic methane and biogenic methane were identified as sources of the carbon. Chemoherm carbonates and seepage-associated carbonates formed in a focused flow regime have lighter ¹³C values, while others formed in a more diffusive flow regime have slightly enriched C isotope values. Three fluid components were inferred based on the calculation of equilibrium ¹⁸O: clay dehydration water, gas hydrate water and seawater. Calculated equilibrium ¹⁸O values of carbonates from different down-core depths as well as from different precipitation stages show that the ¹⁸O of the precipitating fluid is progressively depleted with time. Dolostones showing a methane-C source and a well constrained O-isotope signature are thought to have formed at depth in the sediment and subsequently became exhumed. Glauconitic sandstones cemented by methane-derived carbonate provide evidence that fluid and solid material have been expelled by the mud volcano.     

A geochemical study on mud volcanoes in the Junggar Basin, China

A comprehensive study was performed to characterize, for the first time, the mud, water, and gases released from onshore mud volcanoes located in the southern margin of the Junggar Basin, northwestern China. Chemical compositions of mud, along with the geology of the basin, suggest that a source of the mud is Mesozoic or Cenozoic shale. Oxygen and H isotope compositions of the released water suggest a local meteoric origin. Combined with the positive Eu anomalies of the water, a large ¹⁸O shift of the water suggests extensive interaction with rocks. Gases discharged from the mud volcanoes are predominantly thermogenic hydrocarbons, and the high δ¹³C values (>+20‰ VPDB) for CO₂ gases and dissolved carbonate in muddy water suggest secondary methanogenesis with CO₂ reduction after oil biodegradation.The enrichments of Eu and ¹⁸O in water and the low thermal gradient of the area suggest that the water-rock interactions possibly occur deeper than 3670 ± 200 m. On the other hand, considering the relationship to the petroleum reservoir around the mud volcanoes, the depth of the gases can be derived from about 3600 m, a depth that is greater than that generally estimated for reservoirs whose gas is characterized by ¹³C-enriched CO₂. Oil biodegradation with CO₂ reduction likely occurs at a shallower depth along the seepage system of the mud volcano. The results contribute to the worldwide data set of gas genesis in mud volcanoes. Moreover, they further support the concept that most terrestrial mud volcanoes release thermogenic gas produced in very deep sediments and may be early indicators of oil biodegradation, an important problem in the petroleum industry.     

New evidence of extensive active mud volcanism in the Anaximander mountains (Eastern Mediterranean): The “ATHINA” mud volcano

A 3000 km² multibeam survey was carried out on the eastern Anaximander Mountains (Mts), (Eastern Mediterranean). The objective was to obtain detailed bathymetry of known mud volcanoes and identify new sites of active mud volcanism in the area. N-NW of the Amsterdam Mud-Volcano (MV) several mounds and cone-like morphological irregularities with a height of few tens of meters to about one hundred meters were detected and considered as potential MVs on the basis of their distinctive backscattered character. A group of two mounds was selected, the northern mound was sampled, documented as active, and named accordingly Athina MV. These new findings strongly support the presence of extensive active mud volcanism in the Anaximander Mountains especially in the area north of the Amsterdam MV.GEM     

Geochemical constraints on the petrogenesis of arc picrites and basalts,New Georgia Group,Solomon Islands

Island arc picrites are restricted to a few localities including the Lesser Antilles, Japan, Vanuatu and the Solomon Islands. The picrite occurrences appear to be linked to the subduction of young, hot oceanic crust and anomalous geotherms. At the Solomon arc, the Australian plate is presently subducted beneath the Pacific plate. A particular feature of the Solomon arc is the subduction of a spreading center (Woodlark Ridge). In the Solomon Islands, picrites only occur in the New Georgia archipelago, located above or close to the subducting Woodlark Ridge. These picrites contain between 12 and 30 wt% MgO, the associated primitive basalts show MgO contents from 11.5 to 13.6 wt%. Linear trends defined by Cr, Ni and other trace elements vs. MgO indicate that the picritic bulk compositions originate from mixing between a basaltic-picritic melt and a Mg- and Cr-rich endmember, rather than from fractional crystallization of extremely Mg-rich magmas. Major and trace element modeling identify mantle wedge peridotite as the most likely mixing endmember. Trace element abundances in the Solomon arc picrites indicate a mantle source enrichment by subduction components and a large depletion of Nb and Ta that is typical for island arc volcanic rocks. Most incompatible trace element patterns of the New Georgia picrites and basalts are parallel, supporting a cogenetic evolution of these rocks by mixing processes. ⁸⁷Sr/⁸⁶Sr and Nd values in the basalts and picrites range from 0.7033 to 0.7043 and +5.8 to +8.0, respectively. These values partially overlap with compositions of the Indian MORB field. Alternatively, subducted sediment and fluids from altered MORB may have displaced the Sr isotope composition to more radiogenic ⁸⁷Sr/⁸⁶Sr. Hf values range from +12.2 to +14.6 and show in combination with Nd that the picrites were most likely generated within the Indian mantle domain.This revised version was published online September 2004 with a correction to Table 2.     

Nd and Sr isotope systematics of the Oka complex,Quebec, and their bearing on the evolution of the sub-continental upper mantle

A detailed isotopic study of minerals and whole rocks from the Cretaceous Oka complex, Quebec, Canada, shows a very small variation in initial Nd and Sr isotopic compositions. Assuming an age of 109 Ma for the complex, apatite, calcite, garnet, melilite, monticellite, olivine and pyroxene and whole rocks yield a range for initial ⁸⁷Sr/⁸⁶Sr of 0.70323–0.70333; and for initial ¹⁴³Nd/¹⁴⁴Nd of 0.51271–0.51284 ( _SR(T)= –14.8 to –16.2; _Nd(T)=+4.1 to +6.6). The negative _SR and positive _Nd indicate derivation of the Nd and Sr from a source with a time-integrated depletion in the large-ion lithophile (LIL) elements. This agrees with data from other Canadian carbonatites and confirms that a large part of the Canadian Shield is underlain by a source region depleted in the LIL elements. The new data from Oka suggest that the depleted source may have remained coupled to the continental crust until recent time.     

Sulfur isotope ratios of Icelandic rocks

Sulfur isotope ratios have been determined in 27 selected volcanic rocks from Iceland together with their whole rock chemistry. The ³⁴S of analyzed basalts ranges from –2.0 to +0.4 with an average value of –0.8 Tholeiitic and alkaline rocks exhibit little difference in ³⁴S values but the intermediate and acid rocks analyzed have higher ³⁴S values up to +4.2 It is suggested that the overall variation in sulfur isotope composition of the basalts is caused by degassing. The small range of the ³⁴S values and its similarity to other oceanic and continental basalts, suggest that the depleted mantle is homogeneous in its sulfur isotope composition. The ³⁴S of the depleted mantle is estimated to be within the range for undegassed oceanic basalts, –0.5 to +1.0     

Non-monotonic chemical and O,Sr, Nd,and Pb isotope zonations and heterogeneity in the mafic- to silicic-composition magma chamber of the Grizzly Peak Tuff,Colorado

Strong compositional zonation of the 34 Ma Grizzly Peak Tuff in west-central Colorado is attended by non-monotonic trends in O, Sr, Nd, and Pb isotope ratios. Fiamme from the tuff cluster in chemical compositions and petrographic characteristics, indicating the magma chamber was not continuously zoned but consisted of at least seven compositional layers. The most mafic magma erupted (57 wt% SiO₂, fiamme group 7) had ¹⁸O= +8.5, initial ⁸⁷Sr/⁸⁶Sr=0.7099, _Nd, and ²⁰⁶Pb/²⁰⁴Pb=17.80, suggesting that the magma was produced by 50% fractional crystallization of basaltic magma that assimilated 20 to 40 wt% Proterozoic crust. Isotopic compositions of more evolved parts of the chamber (up to 77 wt% SiO₂, fiamme group 1) depart from the mafic base-level composition of fiamme group 7, and reflect late-stage assimilation that occurred largely after compositional layering was established. ¹⁸O values decrease by as much as 1.5 from fiamme groups 7 through 4, indicating assimilation of hydrothermally altered roof rocks. ¹⁸O values abruptly inerease by up to 1.5 between fiamme groups 4 and 3. This discontinuity is interpreted to reflect evolution in an asymmetric chamber that had a split-level roof, allowing assimilation of wall rocks that varied vertically in degree of hydrothermal alteration. This chamber geometry is also supported by collapse structures in the caldera. Late-stage assimilation of heterogeneous wall rocks is also indicated by variations in Sr, Nd, and Pb isotope ratios. Large Sr isotope disequilibrium exists between some phenocrysts and whole-rock fiamme, and initial ⁸⁷Sr/⁸⁶Sr ratios in phenocrysts are as high as 0.7170. values regularly increase from-13.0 in fiamme group 7 to-11.3 in fiamme group 3, and then decrease to-12.2 in fiamme group 1. ²⁰⁶Pb/²⁰⁴Pb ratios generally increase from 17.80 to 17.94 for fiamme groups 7 through 1. The rhyolitic parts of the Grizzly Peak Tuff have isotopic compositions that could be attributed to a purely crustal melt. It is unlikely, however, that the mafic parts of the tuff were generated by crustal melting, and the compositional and isotopic variations across the entire zonation of the tuff are best explained by fractional crystallization of mantle-derived magmas, accompanied by extensive assimilation of Proterozoic crust.     

Trace-element and Sr,Nd, Pb,and O isotopic composition of Pliocene and Quaternary alkali basalts of the Patagonian Plateau lavas of southernmost South America

The Pliocene and Quaternary Patagonian alkali basalts of southernmost South America can be divided into two groups. The cratonic basalts erupted in areas of Cenozoic plateau volcanism and continental sedimentation and show considerable variation in ⁸⁷Sr/⁸⁶Sr (0.70316 to 0.70512), ¹⁴³Nd/¹⁴⁴Nd (_Nd) and ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb ratios (18.26 to 19.38, 15.53 to 15.68, and 38.30 to 39.23, respectively). These isotopic values are within the range of oceanic island basalts, as are the Ba/La, Ba/Nb, La/Nb, K/Rb, and Cs/Rb ratios of the cratonic basalts. In contrast, the transitional basalts, erupted along the western edge of the outcrop belt of the Pliocene and Quaternary plateau lavas in areas that were the locus of earlier Cenozoic Andean orogenic arc colcanism, have a much more restricted range of isotopic composition which can be approximated by ⁸⁷Sr/⁸⁶Sr=0.7039±0.0004, _Nd, ²⁰⁶Pb/²⁰⁴Pb=18.60±0.08, ²⁰⁷Pb/²⁰⁴Pb=15.60±0.01, and ²⁰⁸Pb/²⁰⁴Pb=38.50±0.10. These isotopic values are similar to those of Andean orogenic are basalts and, compared to the cratonic basalts, are displaced to higher ⁸⁷Sr/⁸⁶Sr at a given ¹⁴³Nd/¹⁴⁴Nd and to higher ²⁰⁷Pb/²⁰⁴Pb at a given ²⁰⁸Pb/²⁰⁴Pb. The transitional basalts also have Ba/La, Ba/Nb, La/Nb, and Cs/Rb ratios higher than the cratonic and oceanic island basalts, although not as high as Andean orogenic are basalts. In contrast to the radiogenic isotopes, ¹⁸O values for both groups of the Patagonian alkali basalts are indistinguishable and are more restricted than the range reported for Andean orogenic are basalts. Whole rock ¹⁸O values calculated from mineral separates for both groups range from 5.3 to 6.5, while measured whole rock ¹⁸O values range from 5.1 to 7.8. The trace element and isotopic data suggest that decreasing degrees of partial melting in association with lessened significance of subducted slabderived components are fundamental factors in the west to east transition from arc to back-arc volcanism in southern South America. The cratonic basalts do not contain the slab-derived components that impart the higher Ba/La, Ba/Nb, La/Nb, Cs/Rb, ⁸⁷Sr/⁸⁶Sr at a given ¹⁴³Nd/¹⁴⁴Nd, ²⁰⁷Pb/²⁰⁴Pb at a given ²⁰⁸Pb/²⁰⁴Pb, and ¹⁸O to Andean orogenic arc basalts. Instead, these basalts are formed by relatively low degrees of partial melting of heterogeneous lower continental lithosphere and/or asthenosphere, probably due to thermal and mechanical pertubation of the mantle in response to subduction of oceanic lithosphere below the western margin of the continent. The transitional basalts do contain components added to their source region by either (1) active input of slab-derived components in amounts smaller than the contribution to the mantle below the arc and/or with lower Ba/La, Ba/Nb, La/Nb, and Cs/Rb ratios than below the arc due to progressive downdip dehydration of the subducted slab; or (2) subarc source region contamination processes which affected the mantle source of the transitional basalts earlier in the Cenozoic.     

New data on the material composition of mud volcano products on Kerch Peninsula

The results of recent studies of the isotope and chemical composition of the waters and breccias that erupted from mud volcanoes of Kerch Peninsula are presented. It was found that the waters of the volcanoes considered were characterized by low salinity, a chloride–hydrocarbonate–sodium composition, and an increased ¹⁸O content. The breccias were enriched in organic matter and some microelements (Li, Se, Hg, etc.). As for petrogenic elements, depletion of Ca in the breccias is noted.     

Olivine clinopyroxenite xenoliths in the Oslo Rift,SE Norway

Olivine clinopyroxenite xenoliths in a basalt flow at Krokskogen in the Oslo rift consist mainly of Al-Ti-rich clinopyroxene and alteration products after olivine (possibly also orthopyroxene). The clinopyroxene contains primary inclusions of Cr-Al-bearing titanomagnetite, pyrite and devitrified glass, and secondary fluid inclusions rich in CO₂. On the basis of petrography, mineral compositions and bulk major and trace element chemistry, it is concluded that the xenoliths represent cumulates with about 5% trapped liquid, formed from a mildly alkaline basaltic magma. Microthermometrical analysis of secondary or pseudosecondary fluid inclusions give a minimum pressure of formation of 5.5 to 6 kbars, that is a depth greater than 16–17 km. The host lava has initial _Nd=+4.16±0.17 and _Sr=–5.50±0.26, which is believed to reflect the isotopic composition of the lithospheric mantle source region under south Norway in early Permian time. The isotopic character of the magma which gave rise to the xenoliths is preserved in clinopyroxenes which have _Nd ^t =+1.9 to +2.6 and _Sr ^t = –1.1 to –1.8. The isotopic differences between the host magma and the xenoliths reflect some degree of crustal contamination of the xenolith's parent magma.The xenoliths of this study represent an important source of information about the large masses of dense cumulates found at depth in the crust under the Oslo rift.