Suchergebnisse

Volcanic and geothermal areas are important emitters of natural gas compounds into the atmosphere, which can be of concern when discharging close to densely, populated sites. Mercury has a strong environmental impact, its organic and inorganic complexes being toxic. The dominant form of Hg in the atmosphere is gaseous elemental mercury (GEM), which has high volatility and residence time of 1-2 years. Volcanic degassing accounts for a significant part of the natural mercury emissions. No mercury limits or target values in ambient air are present in the EU legislations, whereas US-EPA and ATSDR impose 300 and 200 ng/m3, respectively, as a limit for chronic exposure. WHO has proposed the annual average value of 1,000 ng/m3 as a guideline for Hg0 in ambient air. The determination of Hg0 concentrations is often performed via passive/diffusive samplers, which provide time-integrated gas concentrations, but not able to assess the highly variable distributions of GEM. Different weather factors and photochemical reactions indeed affect the Hg0 dispersion. In volcanic/geothermal sites, GEM measurements can be associated with H2S, an irritating and suffocating substance and detectable at very low concentrations (7 μg/m3, ~5 ppb) due to its typical rotten eggs odor. WHO recommends a guideline value of 150 μg/m3 (~107 ppb) with a 24h averaging time. In April 2014 real-time Hg0 and H2S measurements in air were conducted at the Solfatara Crater, which is nested in the town of Pozzuoli (Southern Italy). The main aims were to (1) test this new methodological approach and (2) investigate the Hg0 the H2S concentrations and their spatial distribution. GEM and H2S continuous measurements were determined with a portable Zeeman atomic absorption spectrometer with high frequency modulation of light polarization (Lumex RA-915M, DL: 2ng/m3) and a pulsed fluorescence gas analyzer (Thermo 450i, DL: 1 ppb), respectively. The GEM and H2S and meteorological data were acquired along previously planned pathways at an average speed <5 km/h. The Hg0 and H2S concentrations were between 12 and 77 ng/m3 and 0.2 and 2400 ppb, respectively. The highest measured concentrations corresponded to the main gas discharging areas, whereas the lowest values were measured outside the crater and in the vegetated areas. The results of this study indicate that this technique approach is highly efficient and effective and provides reliable and reproducible Hg0 and H2S concentrations, which can be used to define the exposure that tourists and inhabitants, living close to volcanic and geothermal areas, may suffer.

Nyamulagira, in the Virunga volcanic province (VVP), Democratic Republic of Congo, is one of the most active volcanoes in Africa. The volcano is located about 25 km north-northwest of Lake Kivu in the Western Branch of the East African Rift System (EARS). The activity is characterized by frequent eruptions (on average, one eruption every 2–4 years) which occur both from the summit crater and from the flanks (31 flank eruptions over the last 110 years). Due to the peculiar low viscosity of its lava and its location in the floor of the rift, Nyamulagira morphology is characterized by a wide lava field that covers over 1100 km2 and contains more than 100 flank cones. Indeed, Nyamulagira is a SiO2- undersaturated and alkali-rich basaltic shield volcano with a 3058 m high summit caldera with an extension of about 2 km in diameter. In November 2014 a field expedition was carried out at Nyamulagira volcano and we report here the first assessment of the plume composition and volatile flux from Nyamulagira volcano. Helicopter flights and field observations allowed us to recognize the presence of lava fountains inside an about 350-meter wide pit crater. The lava fountains originated from an extended area of about 20 to 40 m2, in the northeast sector of the central caldera. A second smaller source, close to the previous described one, was clearly visible with vigorous spattering activity. There was no evidence of a lave lake but the persistence of intense activity and the geometry of the bottom of the caldera might evolve in a new lava lake. Using a variety of in situ and remote sensing techniques, we determined the bulk plume concentrations of major volatiles, halogens and trace elements. We deployed a portable MultiGAS station at the rim of Nyamulagira crater, measuring (at 0.5 Hz for about 3 hours) the concentrations of major volcanogenic gas species in the plume (H2O, CO2, SO2, H2S). Simultaneously, scanning differential optical absorption spectroscopy instruments were applied inside the crater as well as downwind the volcano and active alkaline traps (Raschig-Tube and Drechsel bottle) were exposed. The alkaline solution traps acidic species (CO2, SO2, H2S, HCl, HF, HBr, HI) due to the acid-base reactions. Moreover, filter packs technique have also been used to collect both the volatile phase of the plume (sulphur and halogen species) and the particulate phase (major and trace metals) emitted from the volcano. These new results will add to our lacking knowledge of volcanic degassing in VVP, and will increase constraints on the abundances and origins of volatiles from the mantle source which feeds volcanism in the western branch of the EARS.

Exclusive breakup measurements have been performed for the Li6+p system in inverse kinematics at Li6 incident energies of 25 and 29 MeV. The results are considered in the Continuum Discretized Coupled-Channels framework, together with elastic scattering data at 16, 20, 25, and 29 MeV, obtained simultaneously in the same experiment and reported previously. Good agreement between data and theory is observed, interpreted as evidence for strong coupling to the continuum. The direct and sequential (via the Li631+ resonance) breakup cross sections are found to be equally large at the higher incident energies but the dominant effect on the elastic scattering is due to coupling to the sequential breakup. This effect remains dominant even at the lowest energy of 16 MeV, despite the negligible cross section for excitation of the resonance at this low incident energy. ; European Union 262010-ENSAR

Nyamulagira, in the Virunga Volcanic Province (VVP), Democratic Republic of Congo, is one of the most active volcanoes in Africa. The volcano is located about 25 km north-northwest of Lake Kivu in the Western Branch of the East African Rift System (EARS) with a distance of only 15 km to Nyiragongo, which is well known for its decades-old active lava lake. Nyamulagira is a shield volcano with a 3058 m high and 2000 m wide summit caldera. The volcano is characterized by frequent eruptions, which occur both from the summit crater and from the flanks (31 flank eruptions over the last 110 years). Due to the low viscosity lava, although significantly higher than the one of Nyiragongo, wide lava fields cover over 1100 km2 and lava flows often reach > 20 km length. More than 100 flank cones can be counted around the summit crater. A part from its frequent eruptions Nyamulagira had a long period of lava lake activity in the past, at least from 1912 to 1938. During the past decades, gas emissions from Nyamulagira have been only reported during eruptions. This changed in 2012, however, when Nyamulagira began emitting a persistent gas plume above its crater. By the end of 2014, and beginning in 2015, a lava lake was born, a feature that—as of the time of this writing—is still growing. To date, very little is known about gas emissions of Nyamulagira volcano with the only exception for SO2. Very few studies have been conducted regarding the volatile chemistry of Nyamulagira. We try to fill this gap by reporting gas composition measurements of Nyamulagira's volcanic plume during the birth of the lava lake, and in the first year of the lake's activity. Two field surveys have been carried out, the first one on November 1st, 2014 and the second one October 13th – 15th, 2015. Applying the broad toolbox of volcanic gas composition measurement techniques offered us the opportunity to characterize Nyamulagira's plume in excruciating detail. Nyamulagira is known to be a significant emitter of SO2 but shows, perhaps counterintuitively, low CO2/SO2 ratios (min. CO2/SO2 below 0.4). In contrast to Nyiragongo the H2O contribution to the volatile budget of Nyamulagira is high (> 92 % of total gas emissions in 2014). We further determined that molar plume gas ratios of Cl/S, F/S and Br/S all decreased by a factor of two or even more between 2014 and 2015. We will discuss the changes of plume composition in the light of the visually observed evolution of the lava lake and an interpretation on the volcanic system is attempted.