Hydrogen isotope geochemistry and heat balance of a fumarolic system: Kudriavy volcano, Kuriles

The temperature and hydrogen isotope composition of the fumarolic gases have been studied at Kudriavy volcano, Kurile Islands, which is unique for investigating the processes of magma degassing because of the occurrence of numerous easily accessible fumaroles with a temperature range of 100–940°C. There are several local fumarolic fields with a total surface area of about 2600 m2 within the flattened crater of 200×600 m. Each fumarolic field is characterized by the occurrence of high- and low-temperature fumaroles with high gas discharges and steaming areas with lower temperatures. We have studied the thermal budget of the Kudriavy fumarolic system on the basis of the quantitative dependences of the hydrogen isotope ratio (D/H) and tritium concentration on the temperature of fumarolic gases and compared them with the calculated heat balance of mixing between hot magmatic gas and cold meteoric water. Hydrogen isotope composition (δD and 3H) shows a well expressed correlation with the gas temperature. Since D/H ratio and 3H are good indicators of water sources in volcanic areas, it suggests that the thermal budget of the fumarolic system is mostly controlled by the admixing of meteoric waters to magmatic gases. The convective mechanism of heat transfer in the hydrothermal system governs the maximum temperatures of local fumaroles and fumarolic fields. Low-temperature fumaroles at Kudriavy are thermally buffered by the boiling processes of meteoric waters in the mixing zone at pressures of 3–12 bar. These values may correspond to the hydrostatic pressure of water columns about 30–120 m in height in the volcanic edifice and hence to the depth of a mixing/boiling zone. Conductive heat transfer is governed by conductive heat exchange between gases and country rocks and appears to be responsible for the temperature distribution around a local fumarolic vent. The temperature and pressure of shallow degassing magma are estimated to be 1050°C and 2–3 bar, respectively. The length of the ‘main’ fumarolic gas conduit is estimated to be about 80 m from the linear correlation between maximal temperatures of fumarolic fields and distances to the highest-temperature ‘F-940’ fumarole. This value may correspond to the depth of an apical part of the magmatic chamber. The geometry of the crater zone at the Kudriavy summit and the model of convective gas cooling suggest different hydrostatic pressures in the hydrothermal system at the base of high- and low-temperature gas conduits. The depths of gas sources for low-temperature fumaroles are evaluated to be about 200 m at the periphery of the magma chamber

Validation of LA-ICP-MS fluid inclusion analysis with synthetic fluid inclusions

Laser ablation—inductively coupled plasma—mass spectrometry (LA-ICP-MS) has become recognized as a sensitive, efficient, and cost-effective approach to measuring the major-, minor-, and trace-solute compositions of individual fluid inclusions in minerals. As a prerequisite for the routine analysis of natural inclusions in our laboratory, the precision and accuracy of the technique was assessed using sets of multi-element synthetic fluid inclusions. Five multi-element standard solutions were prepared, and incorporated as fluid inclusions in quartz crystals at 750 °C and 7 kbar. Fluid inclusions were ablated with a 193 nm ArF excimer laser and analyzed with a quadrupole ICP-MS, equipped with an octopole reaction cell for the removal of Ar-based interferences. The internal standard used in all cases was Na. Analytical precision for K, Rb, and Cs is typically better than 15% RSD, whereas Li, Mg, Ca, Sr, Ba, Mn, Fe, Cu, Zn, and Cl analyses are typically reproducible within 30% RSD. Measured concentrations approximate a Gaussian distribution, suggesting that analytical errors are random. Analyses for most elements are accurate within 15%. Limits of detection vary widely according to inclusion volume, but are 1 to 100 μfor most elements. These figures of merit are in excellent agreement with previous studies. We also demonstrate that, over the range investigated, precision and accuracy are insensitive to inclusion size and depth. Finally, the combination of our LA-ICP-MS analyses with microthermometric data shows that charge-balancing to NaCl-H2O equivalent chloride molality is the most valid approach to LA-ICP-MS data reduction, where chloride-dominated fluid inclusions are concerned