Boron isotopic composition of fumarolic condensates and sassolites from Satsuma Iwo-jima,Japan

¹¹B/¹⁰B ratios of the high temperature fumarolic gases (>465°C) of this island were found to be constant within the limits of experimental error (¹¹B/¹⁰B = 4.066). This value may represent the ¹¹B/¹⁰B ratio of boron in the andesite magma. ¹¹B/¹⁰B ratios of the low temperature fumarolic gases (<235°C) were found to vary from 4.053 to 4.077. ¹¹B/¹⁰B ratios of some sassolites were approximately equal to that of the fumarolic condensates and the other ones were slightly enriched in ¹⁰B compared to the fumarolic condensates.     

Boron isotopic composition of fumarolic condensates from some volcanoes in Japanese island arcs

Boron samples from 40 fumarolic condensates from volcanoes in the Ryukyu arc (Satsuma Iwo-jima and Shiratori Iwo-yama) and the North-east Japan arc (Usu-shinzan, Showa-shinzan, Esan and Issaikyo-yama) all have ${}^{11}\text{B}{}^{10}\text{B}$ ratios close to 4.07. Higher values, from 4.09 to 4.13, were only observed in condensates from volcanoes in the southernmost end of the North-east Japan arc (Nasu-dake), the northern part of the Izu-Bonin arc (Hakone), and the North Mariana arc (Ogasawara Iwo-jima). These higher values suggest geological interaction of the magmas with sea-water enriched in ¹¹B.     

Reactions governing the chemistry of crater fumaroles from Vulcano Island,Italy, and implications for volcanic surveillance

More than 200 chemical and isotope analyses of fumarolic fluids collected at the Fossa Grande crater, Vulcano Island, during the 1980s show that the main process controlling these fluids is mixing between the gas released by a magma body and the vapour produced through evaporation of brines of marine origin. Large variations in the relative contribution of these two sources have been observed during the last 10 a. The main species (H₂O and CO₂), the inert gases (He and N₂), and the D content of steam are fixed by the mixing processes; they are therefore the best tracers the fraction of the deep magmatic component in the fumarolic fluids discharged at the surface. In contrast, the “fast” species (H₂ and CO) equilibrate at T,P values close to the outlet temperature and atmospheric pressure, and under redox conditions governed by the SO₂H₂S buffer, as indicated by thermodynamic calculations.Acid gases (HCl, HF, H₂S and SO₂) are partly contributed by the magmatic component and partly produced by the reactions between hot rocks, steam and salts which take place in the “dry” zones surrounding the central magmatic gas column, as suggested by the good agreement between their analytical and theoretical contents.     

Environmental impact of the acid fumarolic plume of a passively degassing volcano (Vulcano Island,Italy)

This paper investigates the role played by the fumarolic plume of a passive degassing volcano in the genesis of rock coatings (RC) and in the introduction and re-distribution of metals and trace elements in the surficial environment. At La Fossa active volcano (Vulcano Island) and in the surrounding environment RC develop owing to exposure of the ground surface to the volcanic acid plume produced by the passive degassing of La Fossa. Significant positive anomalies of a wide variety of metals and trace elements (including Bi, Ag, Se, Te, Sb, Pb, As, Cu, Tl and Cd) were observed either in distal and proximal RC. Most of these anomalies are interpreted to be the result of the transport and subsequent deposition of trace elements, likely to form volatile compounds, in the fumarolic plume. Two main processes seem to control the geochemistry of RC: one is represented by the leaching and subsequent deposition of elements from the proximal toward the distal RC; the other is the direct input of trace elements carried by the emitted volcanic aerosol. The fact that most of the trace elements (particularly Pb, As, Tl, Bi, Te, Se, Cd) enriched in the RC of Vulcano are highly toxic and potentially dangerous to health in high concentration, indicates that the atmospheric metal injection by the quiescently degassing La Fossa volcano together with the subsequent deposition and remobilization by means of surficial waters may represent an environmental hazard that should be taken into account in evaluating the potential impact of volcanic air pollution on human health.     

Genesis of fumarolic emissions as inferred by isotope mass balances: CO2 and water at Vulcano Island, Italy

We have developed a quantitative model of CO₂ and H₂O isotopic mixing between magmatic and hydrothermal gases for the fumarolic emissions of the La Fossa crater (Vulcano Island, Italy). On the basis of isotope balance equations, the model takes into account the isotope equilibrium between H₂O and CO₂ and extends the recent model of chemical and energy two-end-member mixing by Nuccio et al. (1999). As a result, the H₂O and CO₂ content and the δD, δ¹⁸O, and δ¹³C isotope compositions for both magmatic and hydrothermal end-members have been assessed. Low contributions of meteoric steam, added at a shallow depth, have been also recognized and quantified in the fumaroles throughout the period from 1988 to 1998. Nonequilibrium oxygen isotope exchange also seems to be occurring between ascending gases and wall rocks along some fumarolic conduits.The δ¹³C_CO2 of the magmatic gases varies around −3 to 1‰ vs. Peedee belemnite (PDB), following a perfect synchronism with the variations of the CO₂ concentration in the magmatic gases. This suggests a process of isotope fractionation because of vapor exsolution caused by magma depressurization. The hydrogen isotopes in the magmatic gases (−1 to −‰ vs. standard mean ocean water [SMOW]), as well as the above δ¹³C_CO2 value, are coherent with a convergent tectonic setting of magma generation, where the local mantle is widely contaminated by fluids released from the subducted slab. Magma contamination in the crust probably amplifies this effect.The computed isotope composition of carbon and hydrogen in the hydrothermal vapors has been used to calculate the δD and δ¹³C of the entire hydrothermal system, including mixed H₂O-CO₂ vapor, liquid water, and dissolved carbon. We have computed values of about 10‰ vs. SMOW for water and −2 to −6.5‰ vs. PDB for CO₂. On these grounds, we think that Mediterranean marine water (δD_H2O ≈ 10‰) feeds the hydrothermal system. It infiltrates at depth throughout the local rocks, reaching oxygen isotope equilibrium at high temperatures. Interaction processes between magmatic gases and the evolving seawater also seem to occur, causing the dissolution of isotopically fractionated aqueous CO₂ and providing the source for hydrothermal carbon. These results have important implications concerning fluid circulation beneath Vulcano and address the more convenient routine of geochemical surveillance.     

Lichens as bioindicators in volcanic areas: Mt. Etna and Vulcano Island (Italy)

 The aim of this paper is to verify whether lichens have the capacity to accumulate atmospheric contaminators linked to volcanic activity. About 100 lichens were collected in 1994 and 1995 from two active volcanic areas in Italy: Mount Etna and Vulcano Island. Twenty-seven elements were analyzed for each individual lichen using Instrumental Neutronic Activation Analysis and Inductively Coupled Plasma-Mass Spectrometry. Lichen composition reflects the contribution of the volcanic particulate material, and the two areas investigated can be distinguished on the basis of the concentration of some lithophile elements. Moreover, the distribution in lichens of the elements (As, Sb, Br, Pb) – derived from gas emissions (plume, fumaroles) – also shows different geochemical trends on Mt. Etna and Vulcano. Received: 20 April 1998 · Accepted: 4 July 1998     

A simple method for the determination of dissolved gases in natural waters. An application to thermal waters from Vulcano Island.

A new method for the determination of dissolved gas species in natural waters is presented. The method is suitable for field operations and ensures the preservation of the sample until analysis in the laboratory. This method is based on the equilibrium partition of gases between a liquid and a gaseous phase after the introduction of host gas. The host gas used depends on the gas species to be determined and on the technical features of the gas chromatograph. In this work pure Ar has been used. After shaking the sample for 5 min, a portion of gas was taken for gas chromatography analysis. From the concentration of gases in the gaseous phase and taking into account the partitioning coefficients of the various species, it is possible to derive the quantity of dissolved gases per litre of water and the partial pressures of the various gas species in equilibrium with water. This method has been applied to several samples of thermal water from Vulcano island. Helium and CO₂ partial pressures of analysed samples were appreciably higher than those typical of waters in equilibrium with the atmosphere, thus indicating processes of interaction between the volcanic gases and groundwaters.     

Geochemistry of thermal fluids on the volcanic isle of Pantelleria,southern Italy

Chemical analyses of thermal springs and gas emissions on the volcanic island of Pantelleria, southern Italy, suggest the presence, at depth, of a NaCl thermal aquifer near 100°C; 80–90% of the water in this aquifer is fed by rainfall and the remainder of the mixture is seawater. Chemical analyses of the gas emissions reveal that below this shallow aquifer, a deeper hydrothermal degassing system (150°C) may exist. Rising CO₂ causes alterations of the upper aquifer host rocks (mostly pantellerites), favors formation of NaHCO₃ type waters, and causes eventual rpecipitation of CaCO₃ and coprecipitation of MgCO₃ and silica. Comparison of the present chemical data with older data from the literature suggests that the shallow Pantelleria thermal aquifer has increased in salinity and decreased in temperature during the last 25 a. Both effects were apparently caused by increased flow of recent seawater into the system because of increased ground water abstraction in the northern part of the island.     

Low-pH waters discharging from submarine vents at Panarea Island (Aeolian Islands,southern Italy) after the 2002 gas blast: Origin of hydrothermal fluids and implications for volcanic surveillance

A geochemical survey of thermal waters collected from submarine vents at Panarea Island (Aeolian Islands, southern Italy) was carried out from December 2002 to March 2007, in order to investigate (i) the geochemical processes controlling the chemical composition of the hydrothermal fluids and (ii) the possible relations between the chemical features of the hydrothermal reservoir and the activity of the magmatic system. Compositional data of the thermal water samples were integrated in a hydrological conceptual model, which describes the formation of the vent fluid by mixing of seawater, seawater concentrated by boiling, and a deep, highly-saline end-member, whose composition is regulated by water-rock interactions at relatively high temperature and shows clear clues of magmatic-related inputs. The chemical composition of concentrated seawater was assumed to be represented by that of the water sample having the highest Mg content. The composition of the deep end-member was instead calculated by extrapolation assuming a zero-Mg end-member. The Na–K–Ca geothermometer, when applied to the thermal end-member composition, indicated an equilibrium temperature of approximately 300 °C, a temperature in agreement with the results obtained by gas-geothermometry.     

Boron isotopic variations in hydrous rhyolitic melts: a case study from Long Valley,California

In this paper, we present boron isotope analyses of variably degassed rhyolitic glasses from Long Valley, California. The following results indicate that pre-eruptive boron isotopic signatures were preserved in degassed glasses: (1) averaged secondary ionization mass spectrometry (SIMS) measurements of H₂O-rich (~3 wt%) melt inclusions from late erupted Bishop Tuff pumice are indistinguishable from positive thermal ionization mass spectrometry (PTIMS) analysis of vesiculated groundmass glass (¹¹B=+5.0±0.9 and +5.4±5, respectively); (2) SIMS spot-analyses on H₂O-poor obsidian (~0.15 wt% H₂O) from younger Glass Mountain Dome YA (average ¹¹B=+5.2±1.0) overlap with compositionally similar late Bishop Tuff melt inclusions; and (3) four variably degassed obsidian samples from the 0.6 ka Mono Craters (H₂O between 0.74 and 0.10 wt%) are homogeneous with regard to boron (average ¹¹B=+3.2±0.8, MSWD=0.4). Insignificant variations in ¹¹B between early and late Bishop Tuff melt inclusion glasses agree with published experimental data that predict minor ¹¹B depletion in hydrous melts undergoing gas-saturated fractional crystallization. Melt inclusions from two crystal-rich post-caldera lavas (Deer Mountain and South Deadman Dome) are comparatively boron-rich (max. 90 ppm B) and have lower ¹¹B values (average ¹¹B=+2.2±0.8 and –0.4±1.0 ) that are in strong contrast to the boron isotopic composition of post-caldera crystal-poor rhyolites (27 ppm B; ¹¹B=+5.7±0.8). These variations in ¹¹B are too large to be caused by pre-eruptive degassing. Instead, we favor assimilation of ¹¹B depleted low-temperature hydrothermally altered intrusive rocks subsequent to fresh rhyolite recharge.Editorial responsibility: J. HoefsAn erratum to this article can be found at     

Energetics of potential heterotrophic metabolisms in the marine hydrothermal system of Vulcano Island, Italy

Values of overall Gibbs free energy of 144 organic oxidation (respiration) and disproportionation (fermentation) reactions are calculated at the temperatures and chemical compositions that exist in nine submarine vents, sediment seeps and geothermal wells in the hydrothermal system of Vulcano Island, Italy. The organic compounds considered here include four carboxylic acids (formic, acetic, propanoic and lactic), two C₅ aldoses (arabinose and xylose), three C₆ aldoses (galactose, glucose and mannose), and 15 protein-forming amino acids (Ala, Arg, Asp, Glu, Gly, His, Ile, Leu, Lys, Met, Phe, Ser, Thr, Tyr, and Val). Oxidation of these compounds is coupled to five redox pairs: O₂/H₂O, , S⁰/H₂S, and Fe₃O₄/Fe²⁺. Energy yields from potential respiration reactions range from 6 to 118 kJ/mol of electrons transferred and show systematic behavior with respect to the terminal electron acceptor. Overall, respiration with O₂ yields the most energy (98–118 kJ/mol e⁻), followed by reactions with (53– 86 kJ/mol e⁻), magnetite (29–91 kJ/mol e⁻), S⁰ (11–33 kJ/mol e⁻) and (6–34 kJ/mol e⁻). Energy yields show little correlation with organic compound family, but are correlated with fluid pH. Variability in energy yields across the nine sites is greatest for Fe(III) reduction and is primarily influenced by pH and the activity of Fe²⁺. In addition to the potential respiration reactions, the energetics of 24 potential fermentation reactions are also calculated. As expected, fermentation reactions generally yield much less energy than respiration. Normalized to the number of moles of carbon transferred, fermentation yields−8 to 71 kJ/mol C, compared with 16 to 531 kJ/mol C for respiration reactions. All respiration and fermentation reactions, except for methionine (Met) fermentation, are exergonic under the in situ hydrothermal conditions and represent a plethora of potential metabolisms for Vulcano’s diverse thermophilic heterotrophs.     

Chemical composition of precipitation at Mt. Vesuvius and Vulcano Island,Italy: volcanological and environmental implications

Natural precipitation and water samples from passive devices were collected at Mt. Vesuvius and Vulcano Island, Italy, during the period 2004–2006, in order to investigate its possible interactions with fumarolic gases. Evidence of chemical reactions between fumarolic fluids and rain samples before and after its deposition into the sampling devices was found at Vulcano Island. Very low pH values (down to 2.5) and significant amounts of chlorine and sulfate (up to 22 mEq/l) were measured at sampling points located close to the fumarolic field. In contrast, anthropogenic contributions and/or dissolution of aerosols (both maritime and continental) influence the chemistry of rainwaters at Mt. Vesuvius, which show inter-annual variations that are highly consistent with those recorded at the coastal site at Vulcano Island. Chemistry of waters directly exposed to fumarolic fluids may then give useful information about its temporal evolution, holding the signal of the “maximum” chemical event occurred in the meanwhile. In addition, the observation of the health status of vegetation colonizing the immediate surroundings of the fumarolic fields, due to its strong dependence on the interactions with these fluids, may work as a possible biomarker of volcanic activity.     

Carbon-oxygen isotopic geochemistry of the Yangla Cu skarn deposit,SW China: Implications for the source and evolution of hydrothermal fluids

The Yangla Cu deposit is the largest Cu skarn deposit in the Jinshajiang tectonic belt. Based on the detailed observation of crosscutting relationships, three mineralization stages (i.e., pre-ore, ore and supergene) have been identified in the Yangla deposit. The pre-ore stage is dominated by prograde skarn. The ore stage is characterized by the precipitation of hydrous silicate minerals, Fe-oxides, Fe-Cu-Mo-sulfides, quartz and calcite, whose mineral assemblages were formed in the early and late sub-ore stages. The early sub-ore stage is marked by retrograde alteration with the deposition of hydrous silicate minerals (e.g., actinolite, epidote and chlorite), Fe-oxides, abundant Fe-Cu-Mo-sulfides, quartz and minor calcite. Whilst, the late sub-ore stage, associated with silicic and carbonate alteration, is represented by widespread thick quartz or calcite veins with disseminated pyrite, chalcopyrite, galena and sphalerite. We present new carbon-oxygen (C-O) isotopic compositions of the ore-hosting marble and hydrothermal calcite of this deposit. The hydrothermal calcite in the Yangla deposit was precipitated from both the early and late sub-ore stages. Calcite I from the early sub-ore stage is anhedral, and occurs as spot in the skarn or locally replaces the skarn minerals. Calcite II from the late sub-ore stage is distinguished by being coarse-grained, subhedral to euhedral and its occurrence in thick veins. Calcite I contains lower δ¹³C_PDB (−7.0‰ to −5.0‰) and δ¹⁸O_SMOW (7.2‰ to 12.7‰) than Calcite II (δ¹³C_PDB = −4.5‰ to −2.3‰; δ¹⁸O_SMOW = 10.7‰ to 19.4‰). In the δ¹³C_PDB vs. δ¹⁸O_SMOW diagram, the Calcite I and Calcite II data fall close to the igneous carbonatite field and between the fields of igneous carbonatite and marine carbonates, respectively. This suggests a dominantly magmatic origin for the early sub-ore fluids, and there might have been increasing carbonate wall rock involvement towards the late sub-ore stage. The ore-hosting marble (δ¹³C_PDB = −4.8‰ to −0.3‰; δ¹⁸O_SMOW = 10.2‰ to 23.9‰) also shows a positive δ¹³C_PDB vs. δ¹⁸O_SMOW correlation, which is interpreted to reflect the decreasing alteration intensity during the interactions between the hydrothermal fluids and ore-hosting carbonates. Simulated calculation suggests that both the Calcite I and Calcite II precipitated at 350 °C to 250 °C and 250 °C to 150 °C, respectively. We proposed that CO₂ degassing and water/rock interactions were likely the two major processes that precipitated the calcite and led to the observed C-O isotopic features of the Yangla Cu deposit.     

Trace element and isotopic variations in a zoned pluton and associated volcanic rocks,Unalaska Island,Alaska: A model for fractionation in the Aleutian calcalkaline suite

Trace elements, including rare earth elements (REE), exhibit systematic variations in plutonic rocks from the Captains Bay pluton which is zoned from a narrow gabbroic rim to a core of quartz monzodiorite and granodiorite. The chemical variations parallel those in the associated Aleutian calcalkaline volcanic suite. Concentrations of Rb, Y, Zr and Ba increase as Sr and Ti decrease with progressive differentiation. Intermediate plutonic rocks are slightly enriched in light REE (La/Yb=3.45–9.22), and show increasing light REE fractionation and negative Eu anomalies (Eu/Eu^*=1.03–0.584). Two border-zone gabbros have similar REE patterns but are relatively depleted in total REE and have positive Eu anomalies; indicative of their cumulate nature. Initial ⁸⁷Sr/⁸⁶Sr ratios in 8 samples (0.70299 to 0.70377) are comparable to those of volcanic rocks throughout the arc and suggest a mantle source for the magmas. Oxygen isotopic ratios indicate that many of the intermediate plutonic rocks have undergone oxygen isotopic exchange with large volumes of meteoric water during the late stages of crystallization; however no trace element or Sr isotopic alteration is evident.Major and trace element variations are consistent with a model of inward fractional crystallization of a parental high-alumina basaltic magma at low pressures (6 kb). Least-squares approximations and trace element fractionation calculations suggest that differentiation in the plutonic suite was initially controlled by the removal of calcic plagioclase, lesser pyroxene, olivine and Fe-Ti oxides but that with increasing differentiation and water fugacity the removal of sub-equal amounts of sodic plagioclase and hornblende with lesser Fe-Ti oxides effectively drove residual liquids toward dacitic compositions. Major and trace element compositions of aplites which intrude the pluton are not adequately explained by fractional crystallization. They may represent partial melts derived from the island arc crust. Similarities in Sr isotopes, chemical compositions and differentiation trends between the plutonic series and some Aleutian volcanic suites indicates that shallow-level fractional crystallization is a viable mechanism for generating the Aleutian calcalkaline rock series.LDGO Contribution no. 2964     

Hydrogeology of thermal waters in Viterbo area, central Italy

A conceptual hydrogeological model of the Viterbo thermal area (central Italy) has been developed. Though numerous studies have been conducted on its geological, geochemical and geothermal features, there is no generalized picture defining the origin and yield of the hydrothermal system. These latter aspects have therefore become the objectives of this research, which is based on new hydrogeological and geochemical investigations. The geological setting results in the coexistence of overlapped interacting aquifers. The shallow volcanic aquifer, characterized by fresh waters, is fed from the area around the Cimini Mountains and is limited at its base by the semiconfining marly-calcareous-arenaceous complex and low-permeability clays. To the west of Viterbo, vertical upflows of thermal waters of the sulphate-chloride-alkaline-earth type with higher gas contents, are due to the locally uplifted carbonate reservoir, the reduced thickness of the semiconfining layer and the high local geothermal gradient. The hot waters (30–60°C) are the result of deep circulation within the carbonate rocks (0.5–1.8 km) and have the same recharge area as the volcanic aquifer. The upward flow in the Viterbo thermal area is at least 0.1 m³/s. This flow feeds springs and deep wells, also recharging the volcanic aquifer from below.     

Hydrogeochemical and isotopic investigation of the Bursa-Oylat thermal waters, Turkey

The Oylat spa is located 80 km southeast of Bursa and 30 km south of Ineg?l in the Marmara region. With temperature of 40°C and discharge of 45 l/s, the Oylat main spring is the most important hot water spring of the area. Southeast of the spa the Forest Management spring has a temperature of 39.4°C and discharge of 2 l/s. The G?z spring 2 km north of the spa, which is used for therapy of eye disease, and cold waters of the Saadet village springs with an acidic character are the further important water sources of the area. EC values of Main spring and Forest Management hot spring (750–780 μS/cm) are lower than those of Saadet and G?z spring waters (2,070–1,280 μS/cm) and ionic abundances are Ca > Na + K > Mg and SO₄ > HCO₃ > Cl. The Oylat and Sızı springs have low Na and K contents but high Ca and HCO₃ concentrations. According to AIH classification, these are Ca–SO₄–HCO₃ waters. Based on the results of δ¹⁸O, ²H and ³H isotope analyses, the thermal waters have a meteoric origin. The meteoric water infiltrates along fractures and faults, gets heated, and then returns to surface through hydrothermal conduits. Oylat waters do not have high reservoir temperatures. They are deep, circulating recharge waters from higher enhanced elevations. δ¹³C_DIC values of the Main spring and Forest Management hot spring are −6.31 and −4.45‰, respectively, indicating that δ¹³C is derived from dissolution of limestones. The neutral pH thermal waters are about +18.7‰ in δ³⁴S while the sulfate in the cold waters is about +17‰ (practically identical to the value for the neutral pH thermal waters). However, the G?z and Saadet springs (acid sulfate waters) have much lower δ³⁴S values (~+4‰).     

北部湾涠洲岛及斜阳岛火山岩微量元素和同位素地球化学及其构造意义

本文在北部湾内一对姊妹火山岛即涠洲岛及斜阳岛火山地质研究基础上,进一步开展火山岩微量元素和Sr-Nd-Pb同位素,以及地幔橄榄岩Re-Os同位素地球化学研究.岛上早晚两期火山岩均为碱性玄武岩,分别属于碱性橄榄玄武岩和碧玄岩.碧玄岩为玻基斑状结构,舍地幔橄榄岩碎块(一般<1cm),表明为地幔岩浆快速喷出地表冷凝而成,岩浆上升过程中极少演化.火山岩微量元素和Sr-Nd-Pb同位素资料表明,涠洲岛及斜阳岛玄武岩与雷琼及北部湾周边、南海海盆玄武岩类似,具有亏损地幔的Sr、Nd同位素组成与Pb同位素显示的EMII富集地幔特征的Dupal异常,表明岩浆并非来自单一地幔源区,不可与OIB或MORB源区简单类比,也非地幔柱成因,而是由两个不同的地球化学组分混合而成.Re-OS同位素特征也指示地幔橄榄岩捕虏体来源于亏损的岩石圈地幔,而非核幔边界.推测涠洲岛及斜阳岛与雷琼及北部湾周边的岩浆可能是由于南海扩张后大陆裂解-软流圈地幔热物质上涌,与上覆薄而年轻的岩石圈地幔相互作用的产物.     

Strontium isotopic geochemistry of the volcanic rocks and associated megacrysts and inclusions from Ross Island and vicinity,Antarctica

Twelve whole-rock samples of volcanic rocks and a composite of 11 basanitoid samples from Ross Island and vicinity, Antarctica show a narrow range of ⁸⁷Sr/⁸⁶Sr ratios from 0.7030₅ to 0.7033₉. This range is consistent with a model of differentiation from a single parent magma, but the data allow a 30% variation in the ⁸⁷Rb/⁸⁶Sr ratio in the source region if the average ratio is less than 0.057 and if the source region has existed as a closed system for 1.5 b.y. Megacrysts of titaniferous augite, kaersutite, and anorthoclase are isotopically indistinguishable from the host volcanic rocks and therefore are probably cogenetic with the volcanic sequence. A single trachyte sample is isotopically distinct from the rest of the volcanic rocks and probably was contaminated with crustal strontium.Ultramafic and mafic nodules found in association with basanitoids and trachybasalts have ⁸⁷Sr/⁸⁶Sr ratios ranging from 0.7027₅ to 0.7057₅. Several of these nodules exhibit evidence of reaction with the melt and are isotopically indistinguishable from their hosts, but data for seven granulite-facies nodules show an apparent isochronal relationship. Although this isochron may be fortuitous, the resulting age of 158±22 m.y. is similar to ages reported for the voluminous Ferrar Dolerites, and suggests isotopic re-equilibration within the lower crust and upper mantle. These nodules are not genetically related to the Ferrar Dolerites, as evidenced by their lower initial ⁸⁷Sr/⁸⁶Sr ratios.Three ultramafic nodules are texturally and isotopically distinct from the rest of the analyzed nodules. These are friable, have larger ⁸⁷Sr/⁸⁶Sr ratios, and may represent a deeper sampling of mantle rock than the granulite-facies nodules. They were, however, derived at a shallower depth than the alkalic magma. Thus they are not genetically related to either the magma or the granulite-facies nodules.