Beschreibung: One of the major problems in the volcanic surveillance is how data from several techniques can be correlated and used to discriminate between possible precursors of volcanic eruptions and changes related to non-eruptive processes. Gas chemical surveys and measurements of SO 2 emission rates performed in the past (2006–2019) at Lastarria volcano in Northern Chile have revealed a persistent increment of magmatic sourced gas emissions since late November 2012, following a 13 years period of intense ground uplift. In this work, we provide new insights into the gas-chemical evolution of Lastarria’s fumarolic discharges obtained from direct sampling (2006–2019) and SO 2 emission rates using UV camera and DOAS instruments (2018–2019) and link these to pre-existing information on ground deformation (1998–2016) in order to determine the origin of observed degassing and ground deformation processes. We revise the four mechanisms originally proposed as alternatives by Lopez et al. (Geosphere, 2018, 14 (3), 983–1007) to explain the changes observed in the fluid geochemistry and ground deformation between 2009 and 2012, in order to explain major changes in gas-geochemistry over an extended period between 1998 and 2019. We hypothesize that a continuous sequence of processes explains the evolution in the fluid geochemistry of fumarolic discharges. Two mechanisms are responsible of the changes in the gas composition during the studied period, corresponding to a 1) deep magma chamber (7–15 km depth) pressurized by volatile exsolution (1998–2020), which is responsible of the large-scale deformation; followed by 2) a crystallization-induced degassing (2001–2020) and pressurization of the hydrothermal system (2003-early November 2012), where the former process induced the changes in the gas composition from hydrothermal-dominated to magmatic-dominated, whereas the last produced the small-scale deformation at Lastarria volcano. The changes in the gas composition since late November 2012, which were strongly dominated by magmatic volatiles, produced two consecutive processes: 1) acidification (late November 2012–2020) and 2) depletion (2019–2020) of the hydrothermal system. In this work we have shown that a long-term surveillance of the chemistry of fluid discharges provides valuable insights into underlying magmatic/volcanic processes, and consequently, for forecasting future eruptions.

Beschreibung: This work presents the first chemical and isotopic (δ13C-CO2, δ13C-CH4, 3He, 4He, 20Ne, 40Ar, 36Ar, δ18O, and δD) data for fluid discharges fromGuallatiri volcano, a remote and massive stratovolcano, which is considered as the second most active volcano of the Central Volcanic Zone (CVZ) in northern Chile. Fumarolic gases had outlet temperatures of between 80.2 and 265 °C, and showed a significant magmatic fluid contribution marked by the occurrence of SO2, HCl, and HF that are partially scrubbed by a hydrothermal aquifer. The helium isotope ratios (〈 3.2) were relatively low compared to those of other active volcanoes in CVZ, possibly due to contamination of the magmatic source by 4He-rich crust and/or crustal fluid addition to the hydrothermal reservoir. Geothermometry in the H2O-CO2-CO-H2-CH4 system suggests equilibrium temperatures of up to 320 °C attained in a vapor phase at redox conditions intermediate between those typical of hydrothermal and magmatic environments. Thermal springs located 12 km northwest of the volcano’s summit had outlet temperatures of up to 50.1 °C, neutral to slightly basic pH, and a sodium bicarbonate composition, typical of distal fluid discharges in volcanic systems. Cold springs at the base of the volcanic edifice, showing a calcium sulfate composition, were likely produced by interaction of shallow meteoric water with CO2- andH2S-rich gases. A geochemical conceptual model was constructed to graphically represent these results, which can be used as an indication for future geochemical monitoring and volcanic hazard assessment.

Beschreibung: Published

Beschreibung: id 57

Beschreibung: 2V. Struttura e sistema di alimentazione dei vulcani

Beschreibung: 4V. Processi pre-eruttivi

Beschreibung: JCR Journal

Beschreibung: Recent geophysical evidence for large-scale regional crustal inflation and localized crustal magma intrusion has made Lastarria volcano (northern Chile) the target of numerous geological, geophysical, and geochemical studies. The chemical composition of volcanic gases sampled during discrete campaigns from Lastarria volcano indicated a well-developed hydrothermal system from direct fumarole samples in A.D. 2006, 2008, and 2009, and shallow magma degassing using measurements from in situ plume sampling techniques in 2012. It is unclear if the differences in measured gas compositions and resulting interpretations were due to artifacts of the different sampling methods employed, short-term excursions from baseline due to localized changes in stress, or a systematic change in Lastarria’s magmatic-hydrothermal system between 2009 and 2012. Integrated results from a two-day volcanic gas sampling and measurement campaign during the 2014 International Association of Volcanology and Chemistry of the Earth’s Interior (IAVCEI) Commission on the Chemistry of Volcanic Gases (CCVG) 12th Gas Workshop are used here to compare and evaluate current gas sampling and measurement techniques, refine the existing subsurface models for Lastarria volcano, and provide new constraints on its magmatic-hydrothermal system and total degassing budget. While compositional differences among sampling methods are present, distinct compositional changes are observed, which if representative of longterm trends, indicate a change in Lastarria’s overall magmatic-hydrothermal system. The composition of volcanic gases measured in 2014 contained high proportions of relatively magma- and water-soluble gases consistent with degassing of shallow magma, and in agreement with the 2012 gas composition. When compared with gas compositions measured in 2006–2009, higher relative H2O/CO2 ratios combined with lower relative CO2/St and H2O/St and stable HCl/St ratios (where St is total S [SO2 + H2S]) are observed in 2012 and 2014. These compositional changes suggest variations in the magmatic-hydrothermal system between 2009 and 2012, with possible scenarios to explain these trends including: (1) decompression-induced degassing due to magma ascent within the shallow crust; (2) crystallization-induced degassing of a stalled magma body; (3) depletion of the hydrothermal system due to heating, changes in local stress, and/or minimal precipitation; and/or (4) acidification of the hydrothermal system. These scenarios are evaluated and compared against the geophysical observations of continuous shallow inflation at ~8 km depth between 1997 and 2016, and near-surface (〈1 km) inflation between 2000 and 2008, to further refine the existing subsurface models. Higher relative H2O/CO2 observed in 2012 and 2014 is not consistent with the depletion or acidification of a hydrothermal system, while all other observations are consistent with the four proposed models. Based on these observations, we find that scenarios 1 or 2 are the most likely to explain the geochemical and geophysical observations, and propose that targeted shallow interferometric synthetic-aperture radar (InSAR) studies could help discriminate between these two scenarios. Lastly, we use an average SO2 flux of 604 ± 296 t/d measured on 22 November 2014, along with the average gas composition and diffuse soil CO2 flux measurements, to estimate a total volatile flux from Lastarria volcano in 2014 of ~12,400 t/d, which is similar to previous estimates from 2012.

Beschreibung: Published

Beschreibung: 983–1007

Beschreibung: 2V. Struttura e sistema di alimentazione dei vulcani

Beschreibung: 2IT. Laboratori sperimentali e analitici

Beschreibung: JCR Journal

Beschreibung: This work presents chemical and isotopic (δ13C-CO2, δ13C-CH4, 3He, 4He, 20Ne, 40Ar, 36Ar, δ18O and δD) data on fluid discharges from the Colpitas-Taapaca volcanic-hydrothermal system, located close to the Taapaca Volcanic Complex, with the aim to investigate the physical-chemical conditions of the fluid source and to provide a preliminary evaluation of the geothermic potential of the study area. Colpitas thermal springs (to 56 °C) and part of the cold springs (≤18°C) from this area have a Na+-Cl- composition and Total Dissolved Solids (TDS) values (from 6,059 to 19,118 mg/L). Putre springs also show a Na+-Cl- composition, TDS values up to 7,887 mg/L, and outlet temperatures from 21 to 31 °C. Colpitas cold springs, with a Ca2+-SO4 2- composition and relatively low TDS values (≤1,350 mg/L), are likely produced by interaction of shallow water with uprising H2S-rich hydrothermal gases. This process is likely also controlling the chemistry of Jurase thermal springs, which have the highest outlet temperatures of the study area (up to 68 °C), a Ca2+-SO4 2- composition and TDS values ≤2,355 mg/L. Eventually, Las Cuevas springs have temperatures up to 36 °C, a Na+-HCO3 - composition and low TDS values (≤1,067 mg/L), typical features of springs related to a shallow aquifer. The δ18OH 2O and δD-H2O values indicate that all waters have a dominant meteoric origin. Enrichments in 18O and D shown by Colpitas and Putre thermal waters are likely due to steam loss and waterrock interaction, masking a possible direct steam contribution from magmatic degassing. Gas emissions from Colpitas bubbling pools are dominated by CO2, with significant concentrations of CH4, H2S and H2. The Rc/Ra values (up to 2.04) of Colpitas gases indicate a significant contribution of magmatic to mantle He, whereas the high CO2/3He ratios, combined with δ13C-CO2 values ranging from -7.66 to -5.63 ‰ vs. PDB, imply a dominant crustal CO2 source, mostly involving limestone. Estimated temperatures based on the composition of waters and gases from Colpitas are up to 215 °C. Higher temperatures (240 °C) are estimated for Putre thermal waters, although these waters, as well as those from Jurase and Las Cuevas, are too immature for a reliable application of geothermometric techniques. Based on the theoretical reservoir temperature and the measured Cl total output, the thermal energy released from Colpitas thermal area is estimated at up to 13.9 Mw. Such results suggest the occurrence of a promising heat source, possibly related to Taapaca volcanic complex, and encourage the development of future research based on combined geophysical and geochemical approaches, in order to provide a reliable evaluation of the geothermal potential of the whole area.

Beschreibung: Published

Beschreibung: 359-373

Beschreibung: 2V. Struttura e sistema di alimentazione dei vulcani

Beschreibung: JCR Journal

Beschreibung: An external skeleton is an essential part of the body plan of many animals and is thought to be one of the key factors that enabled the great expansion in animal diversity and disparity during the Cambrian explosion. Molluscs are considered ideal to study the evolution of biomineralization because of their diversity of highly complex, robust and patterned shells. The molluscan shell forms externally at the interface of animal and environment, and involves controlled deposition of calcium carbonate within a framework of macromolecules that are secreted from the dorsal mantle epithelium. Despite its deep conservation within Mollusca, the mantle is capable of producing an incredible diversity of shell patterns, and macro- and micro-architectures. Here we review recent developments within the field of molluscan biomineralization, focusing on the genes expressed in the mantle that encode secreted proteins. The so-called mantle secretome appears to regulate shell deposition and patterning and in some cases becomes part of the shell matrix. Recent transcriptomic and proteomic studies have revealed marked differences in the mantle secretomes of even closely-related molluscs; these typically exceed expected differences based on characteristics of the external shell. All mantle secretomes surveyed to date include novel genes encoding lineage-restricted proteins and unique combinations of co-opted ancient genes. A surprisingly large proportion of both ancient and novel secreted proteins containing simple repetitive motifs or domains that are often modular in construction. These repetitive low complexity domains (RLCDs) appear to further promote the evolvability of the mantle secretome, resulting in domain shuffling, expansion and loss. RLCD families further evolve via slippage and other mechanisms associated with repetitive sequences. As analogous types of secreted proteins are expressed in biomineralizing tissues in other animals, insights into the evolution of the genes underlying molluscan shell formation may be applied more broadly to understanding the evolution of metazoan biomineralization.

Beschreibung: Lascar (5592 m a.s.l.) and Lastarria (5697 m a.s.l.) are Chilean active stratovolcanoes located in the Central Volcanic Zone (CVZ; 16°S to 28°S) that have developed on top of a 71 km thick continental crust. Independently of the similarities in their Plinian/Vulcanian eruptive styles, their complex magmatic feeding structures and the origins of their magmatic fluids still necessitate constraints in order to improve the reliability of geochemical monitoring. Here we investigate the petrography, bulk-rock chemistry, and mineral chemistry in products from the 1986–1993 explosive eruptive cycle at Lascar and from several Holocene eruptive sequences at Lastarria. These data are integratedwith measurements of the noble gas isotopes in fluid inclusions (FIs) of minerals fromthe same products as well as in fumarole gases. The geochemistry ofminerals and rocks shows that the studied products belong to high-K–calc-alkaline series typical of subduction-related settings, and provide evidence of differentiation,mixing, and crustal assimilation that are higher at Lastarria. The contribution of slab sediments and fluids to magma genesis in thewedge is limited, suggesting a homogeneous mantle beneath CVZ. The deepest crystallization processes occurred at variable levels of the plumbing systems according to the lithostatic equivalent depths estimated with mineral equilibrium geobarometers at Lascar (15–29 km) and Lastarria (~20–40 km). The 40Ar/36Ar and 4He/20Ne ratios in FIs and fumarole gases indicate the presence of some degree of air contamination in the fluids from both volcanoes. The 3He/4He values at Lascar (6.9–7.3 Ra) are relatively homogeneous and comparable to those of fumaroles, suggesting a main zone of magma crystallization and degassing. In contrast, the 3He/4He values at Lastarria (5.31–8.01 Ra) vary over a wide range, suggesting various magma storage levels and providing evidence of crustal contamination, as indicated by the rock chemistry.We argue thatmantle beneath the two volcanoes has a MORB-like signature of 3He/4He, while local crustal contamination explains the lower ratios measured at Lascar.

Beschreibung: Published

Beschreibung: 105615

Beschreibung: 1V. Storia eruttiva

Beschreibung: 2V. Struttura e sistema di alimentazione dei vulcani

Beschreibung: JCR Journal

Beschreibung: © The Author(s), 2022. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Barry, P. H., De Moor, J. M., Chiodi, A., Aguilera, F., Hudak, M. R., Bekaert, D. V., Turner, S. J., Curtice, J., Seltzer, A. M., Jessen, G. L., Osses, E., Blamey, J. M., Amenabar, M. J., Selci, M., Cascone, M., Bastianoni, A., Nakagawa, M., Filipovich, R., Bustos, E., Schrenk, M. O. , Buongiorno, J., Ramírez, C. J., Rogers, T. J., Lloyd, K. G. & Giovannelli, D. The helium and carbon isotope characteristics of the Andean Convergent Margin. Frontiers in Earth Science, 10, (2022): 897267, https://doi.org/10.3389/feart.2022.897267.

Beschreibung: Subduction zones represent the interface between Earth’s interior (crust and mantle) and exterior (atmosphere and oceans), where carbon and other volatile elements are actively cycled between Earth reservoirs by plate tectonics. Helium is a sensitive tracer of volatile sources and can be used to deconvolute mantle and crustal sources in arcs; however it is not thought to be recycled into the mantle by subduction processes. In contrast, carbon is readily recycled, mostly in the form of carbon-rich sediments, and can thus be used to understand volatile delivery via subduction. Further, carbon is chemically-reactive and isotope fractionation can be used to determine the main processes controlling volatile movements within arc systems. Here, we report helium isotope and abundance data for 42 deeply-sourced fluid and gas samples from the Central Volcanic Zone (CVZ) and Southern Volcanic Zone (SVZ) of the Andean Convergent Margin (ACM). Data are used to assess the influence of subduction parameters (e.g., crustal thickness, subduction inputs, and convergence rate) on the composition of volatiles in surface volcanic fluid and gas emissions. He isotopes from the CVZ backarc range from 0.1 to 2.6 RA (n = 23), with the highest values in the Puna and the lowest in the Sub-Andean foreland fold-and-thrust belt. Atmosphere-corrected He isotopes from the SVZ range from 0.7 to 5.0 RA (n = 19). Taken together, these data reveal a clear southeastward increase in 3He/4He, with the highest values (in the SVZ) falling below the nominal range associated with pure upper mantle helium (8 ± 1 RA), approaching the mean He isotope value for arc gases of (5.4 ± 1.9 RA). Notably, the lowest values are found in the CVZ, suggesting more significant crustal inputs (i.e., assimilation of 4He) to the helium budget. The crustal thickness in the CVZ (up to 70 km) is significantly larger than in the SVZ, where it is just ∼40 km. We suggest that crustal thickness exerts a primary control on the extent of fluid-crust interaction, as helium and other volatiles rise through the upper plate in the ACM. We also report carbon isotopes from (n = 11) sites in the CVZ, where δ13C varies between −15.3‰ and −1.2‰ [vs. Vienna Pee Dee Belemnite (VPDB)] and CO2/3He values that vary by over two orders of magnitude (6.9 × 108–1.7 × 1011). In the SVZ, carbon isotope ratios are also reported from (n = 13) sites and vary between −17.2‰ and −4.1‰. CO2/3He values vary by over four orders of magnitude (4.7 × 107–1.7 × 1012). Low δ13C and CO2/3He values are consistent with CO2 removal (e.g., calcite precipitation and gas dissolution) in shallow hydrothermal systems. Carbon isotope fractionation modeling suggests that calcite precipitation occurs at temperatures coincident with the upper temperature limit for life (122°C), suggesting that biology may play a role in C-He systematics of arc-related volcanic fluid and gas emissions.

Beschreibung: This work was principally supported by the NSF-FRES award 2121637 to PB, KL, and JM. Field work was also supported by award G-2016-7206 from the Alfred P. Sloan Foundation and the Deep Carbon Observatory to PB, KL, DG, and JM. Additional support came from The National Fund for Scientific and Technological Development of Chile (FONDECYT) Grant 11191138 (The National Research and Development Agency of Chile, ANID Chile), and COPAS COASTAL ANID FB210021 to GJ. DG was partially supported by funding from the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation program Grant Agreement No. 948972—COEVOLVE—ERC-2020-STG.