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  • 04. Solid Earth::04.08. Volcanology::04.08.01. Gases
  • Carbon cycle
  • 2015-2019  (72)
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Years
Year
  • 1
    Publication Date: 2024-05-09
    Description: The Principal Cordillera of Central Chile is characterized by two belts of different ages and lithologies: (i) an eastern Mesozoic belt, consisting of limestone- and gypsum-rich sedimentary rocks at the border between Central Chile and Argentina, where the active volcanic arc occurs; and (ii) a western belt of Cenozoic age containing basaltic to andesitic volcanic and volcanoclastic sequences. This distinctive geological setting controls water chemistry of cold and thermal springs in the region, which are fed by meteoric water that circulates through deep regional structures. In the western sector of Principal Cordillera, water–rock interaction processes produce lowTDS, slightly alkaline HCO3 − dominatedwaters, although dissolution of underlyingMesozoic evaporitic rocks occasionally causes SO4 2− and Cl− enrichments. In this area, few Na+–HCO3 − and Na+–SO4 2− waters occurred, being likely produced by a Ca2+–Na+ exchange during water–rock interactions. Differently, the chemical features of Ca2+–Cl−waterswas likely related to an albitization–chloritization process affecting basaltic to andesitic rocks outcropping in this area. Addition of Na+–Cl− brines uprising from the eastern sector through the westverging thrust faults cannot be excluded, as suggested by the occurrence of mantle He (~19%) in dissolved gases. In contrast, in the eastern sector of the study region, mainly characterized by the occurrence of evaporitic sequences and relatively high heat flow,mature Na+–Cl− waters were recognized, the latter being likely related to promising geothermal reservoirs, as supported by the chemical composition of the associated bubbling and fumarolic gases. Their relatively low3He/4He ratios (up to 3.9 Ra)measured in the fumaroles on this area evidenced a significant crustal contamination by radiogenic 4He. The latter was likely due to (i) degassing from 4He-rich magma batches residing in the crust, and/or (ii) addition of fluids interacting with sedimentary rocks. This interpretation is consistent with the measured δ13C-CO2 values (from−13.2 to−5.72‰vs. V-PDB) and the CO2/3He ratios (up to 14.6 × 1010), which suggest that CO2 mostly originates from the limestone-rich basement and recycling of subducted sediments,with an important addition of sedimentary (organic-derived) carbon,whereas mantle degassing contributes at a minor extent. According to geothermometric estimations based on the Na+, K+, Mg2+ and Ca2+ contents, the mature Na+–Cl− rich waters approached a chemical equilibrium with calcite, dolomite, anhydrite, fluorite, albite, K-feldspar and Ca- andMg-saponites at a broad range of temperatures (up to ~300 °C) In the associated gas phase, equilibria of chemical reactions characterized by slowkinetics (e.g. sabatier reaction) suggested significant contributions from hot and oxidizing magmatic gases. This hypothesis is consistent with the δ13C-CO2, Rc/Ra, CO2/3He values of the fumarolic gases. Accordingly, the isotopic signatures of the fumarolic steam is similar to that of fluids discharged from the summit craters of the two active volcanoes in the study area (Tupungatito and Planchón–Peteroa). These results encourage the development of further geochemical and geophysical surveys aimed to provide an exhaustive evaluation of the geothermal potential of these volcanic–hydrothermal systems.
    Description: Published
    Description: 97-113
    Description: 1V. Storia e struttura dei sistemi vulcanici
    Description: JCR Journal
    Description: restricted
    Keywords: Fluid geochemistry ; Central Chile ; Water–gas–rock interaction ; Hydrothermal reservoir ; Geothermal resource ; Volcanoes ; 03. Hydrosphere::03.02. Hydrology::03.02.03. Groundwater processes ; 03. Hydrosphere::03.04. Chemical and biological::03.04.03. Chemistry of waters ; 03. Hydrosphere::03.04. Chemical and biological::03.04.05. Gases ; 03. Hydrosphere::03.04. Chemical and biological::03.04.06. Hydrothermal systems ; 04. Solid Earth::04.04. Geology::04.04.12. Fluid Geochemistry ; 04. Solid Earth::04.08. Volcanology::04.08.01. Gases
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 2
    Publication Date: 2024-05-09
    Description: We have analyzed the carbon isotopic composition of CO2, methane, ethane, propane and n-butane, the hydrogen isotopic composition of methane as well as total concentrations of gas constituents contained in theMediterranean volcanic–hydrothermal discharges of Nisyros (Greece), Vesuvio, La Solfatara, Ischia and Pantelleria (all Italy) to determine the origin of the hydrocarbons. Isotopic criteria conventionally used for hydrocarbon classification suggest thermogenic origins, except for Pantelleria, for which an abiogenic origin is indicated. These findings would imply that thermogenic sources can provide methane/(ethane + propane) concentration ratios as high as those usually observed for microbial hydrocarbons. However, additional consideration of gas concentration data challenges the suitability of conventional criteria for the classification of hydrocarbons emanating from hydrothermal environments. Methane seems to be in close equilibrium with co-occurring CO2, whereas its higher chain homologues are not. Therefore, it cannot be excluded that methane on the one hand and ethane, propane and n-butane on the other hand have distinct origins. The carbon isotopic composition of methane might be controlled by the carbon isotopic composition of co-occurring inorganic CO2 and by hydrothermal temperatures whereas the carbon isotopic composition of the higher n-alkanes could correspond to the maturity of organic matter and/or to the residence time of the gasses in the source system
    Description: Published
    Description: 152–163
    Description: 2V. Dinamiche di unrest e scenari pre-eruttivi
    Description: JCR Journal
    Description: restricted
    Keywords: Hydrocarbons ; Abiogenic ; Thermogenic ; Stable isotopes ; Fumaroles ; 04. Solid Earth::04.04. Geology::04.04.12. Fluid Geochemistry ; 04. Solid Earth::04.08. Volcanology::04.08.01. Gases
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 3
    Publication Date: 2024-05-09
    Description: This study presents the first geochemical data of fluid discharges collected from February 2010 to March 2015 from the Planchón–Peteroa–Azufre Volcanic Complex (PPAVC), located in the Transitional Southern Volcanic Zone (TSVZ) at the border between Argentina and Chile. During the study period, from January 2010 to July 2011, Peteroa volcano experienced phreatic to phreatomagmatic eruption possibly related to the devastating Maule earthquake occurred on February 27, 2010. The compositional dataset includes low temperature (from 43.2 to 102 °C) gas discharges from (i) the summit of Peteroa volcano and (ii) the SE flank of Azufre volcano, both marked by a significant magmatic fluid contribution, as well as bubbling gases located at the foothill of the Peteroa volcanic edifice, which showed a chemical signature typical of hydrothermal fluids. In 2012, strong compositional changes affected the Peteroa gases fromthe summit area: the acidic gas species, especially SO2, increased, suggesting an input of fluids from magma degassing. Nevertheless, the R/Ra and δ13C–CO2 values decreased, which would imply an enhanced contribution from a meteoric-hydrothermal source. In 2014–2015, the chemical and isotopic compositions of the 2010–2011 gases were partially restored. The anomalous decoupling between the chemical and the isotopic parameters was tentatively interpreted as produced by degassing activity from a small batch of dacitic magma that in 2012 masked the compositional signature of the magmatic fluids released from a basalticmagma that dominated the gas chemistry in 2010–2011. This explanation reliably justifies the observed geochemical data, although the mechanisms leading to the change in time of the dominatingmagmatic fluid source are not clear. At this regard, a geophysical survey able to provide information on the location of the two magma batches could be useful to clarify the possible relationships between the compositional changes that affected the Peteroa fluid discharges and the 2010–2011 eruptive activity.
    Description: Published
    Description: 41-53
    Description: 2V. Dinamiche di unrest e scenari pre-eruttivi
    Description: JCR Journal
    Description: restricted
    Keywords: volcanic gas geochemistry ; degassing model ; isotope geochemistry ; 04. Solid Earth::04.08. Volcanology::04.08.01. Gases
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 4
    Publication Date: 2023-11-20
    Description: Active subaerial volcanoes often discharge large amounts of CO2 and H2S to the atmosphere, not only during eruptions but also during periods of quiescence. These gases are discharged through focused (plumes, fumaroles, etc.) and diffuse emissions. Several studies have been carried out to estimate the global contribution of CO2 and H2S emitted to the atmosphere by subaerial volcanism, but additional volcanic degassing studies will help to improve the current estimates of bothCO2 andH2S discharges. In October 2008, a wide-scale survey was carried out at Mt. Etna volcano, one the world’s most actively degassing volcanoes on Earth, for the assessment of the total budget of volcanic/hydrothermal discharges of CO2 and H2S, both from plume and diffuse emissions. Surface CO2 and H2S effluxes were measured by means of the accumulation chamber method at 4075 sites, covering an area of about 972.5 km2. Concurrently, plume SO2 emission at Mt. Etna was remotely measured by a car-borne Differential Optical Absorption Spectrometry (DOAS) instrument. Crater emissions of H2O, CO2 and H2S were estimated by multiplying the plume SO2 emission times the H2O/SO2, CO2/SO2 and H2S/SO2 gas plume mass ratios measured in situ using a portable multisensor. The total output of diffuse CO2 emission from Mt. Etna was estimated to be 20,000 ± 400 t day-1 with 4520 t day-1 of deep-seated CO2. Diffuse H2S output was estimated to be 400 ± 20 kg day-1, covering an area of 9.1 km2 around the summit craters of the volcano. Diffuse H2S emission on the volcano flanks was either negligible or null, probably due to scrubbing of this gas before reaching the surface. During this study, the average crater SO2 emission rate was *2100 t day-1. Based on measured SO2 emission rates, the estimated H2O, CO2 and H2S emission rates from Etna’s crater degassing were 220,000 ± 100,000, 35,000 ± 16,000 and 510 ± 240 t day-1, respectively. These high values are explained in terms of intense volcanic activity at the time of this survey. The diffuse/plume CO2 emission mass ratio at Mt. Etna was *0.57, that is typical of erupting volcanoes (mass ratio\1). The average CO2/SO2 molar ratio measured in the plume was 11.5, which is typical of magmatic degassing at great depth beneath the volcano, and the CO2/H2S mass ratio in total diffuse gas emissions was much higher (*11,000) than in plume gas emissions (*68). These results will provide important implications for estimates of volcanic total carbon and sulfur budget from subaerial volcanoes.
    Description: project CGL2005-07509/CLI, Ministry of Education and Science of Spain
    Description: Published
    Description: 327-349
    Description: 4V. Vulcani e ambiente
    Description: JCR Journal
    Description: restricted
    Keywords: Mt. Etna ; Carbon dioxide ; Hydrogen sulfide ; Gas budget ; Diffuse degassing ; Crater degassing ; 04. Solid Earth::04.08. Volcanology::04.08.01. Gases
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
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  • 5
    Publication Date: 2023-01-16
    Description: With this short communication we address the principal issues raised by Delmelle et al. (2014) in relation to the work of Bagnato et al. (2013) concerning the 2010 eruption of Eyjafjallajo¨ kull, Iceland. The principal conclusions of the work of Bagnato et al. (2013) include the observation that protracted gas-aerosol interaction in the plume promotes selective leaching of cation species from ash, with alkalis and Ca (and, among trace elements, Zn and Cu) being more rapidly re-mobilized (and transferred to soluble surface salts) relative to more inert elements (Mg, Ti). They also observed that adsorption onto ash surfaces is a major atmospheric sink of volcanic acidic gases, with 282 tons of elemental sulfur and 605–691 tons of halogens being daily ground deposited via ash over Iceland in early May 2010. Acidic gas adsorption onto ash increases almost linearly with plume aging (e.g., upon increasing in-plume residence times of ash and gases), and is seen to proceed at about 3 time faster rates for HF than for SO2 and HCl. However, Delmelle et al. (2014) criticized our strategies for data acquisition, processing and interpretation. They also raised some objections concerning several key topics explored by Bagnato et al. (2013), with a special focus on the discussion of rates of interaction between ash particles and gases in a volcanic cloud, and the consequent formation of soluble salts on ash surfaces. They also considered incorrect the estimate of depositional fluxes and volatile budget for the Eyjafjallajo¨ kull eruption. While we appreciate the in-depth analysis of Delmelle et al. (2014), we show that most of their criticisms derive from a partial and sometimes incorrect understanding of the work of Bagnato et al. (2013), which overall led to unsupported conclusions and misleading analysis of the original results. Here, we present a detailed response to the comments of Delmelle et al. (2014), accompanied by additional explicative material. The principal conclusions presented in Bagnato et al. (2013) are given additional support by this complementary note.
    Description: Published
    Description: 385-389
    Description: 5V. Sorveglianza vulcanica ed emergenze
    Description: JCR Journal
    Description: restricted
    Keywords: Eyjafjallajokull ; sulfur, halogens and trace metals ; 04. Solid Earth::04.08. Volcanology::04.08.01. Gases
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
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  • 6
    Publication Date: 2022-10-27
    Description: Author Posting. © American Geophysical Union, 2019. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 46 (2019): 10484–10494, doi:10.1029/2019GL083719.
    Description: Tropical cyclones (hurricanes) generate intense surface ocean cooling and vertical mixing resulting in nutrient upwelling into the photic zone and episodic phytoplankton blooms. However, their influence on the deep ocean remains unknown. Here we present evidence that hurricanes also impact the ocean's biological pump by enhancing export of labile organic material to the deep ocean. In October 2016, Category 3 Hurricane Nicole passed over the Bermuda Time Series site in the oligotrophic NW Atlantic Ocean. Following Nicole's passage, particulate fluxes of lipids diagnostic of fresh phytodetritus, zooplankton, and microbial biomass increased by 30–300% at 1,500 m depth and 30–800% at 3,200 m depth. Mesopelagic suspended particles following Nicole were also enriched in phytodetrital material and in zooplankton and bacteria lipids, indicating particle disaggregation and a deepwater ecosystem response. Predicted climate‐induced increases in hurricane frequency and/or intensity may significantly alter ocean biogeochemical cycles by increasing the strength of the biological pump.
    Description: This work and the Oceanic Flux Program time series were supported by the National Science Foundation Chemical Oceanography Program Grant OCE 1536644. The Bermuda Atlantic Time Series and Hydrostation S time series were supported by NSF Grants OCE 1756105 and OCE 1633125, respectively. We acknowledge the contributions of BATS technicians with CTD and pigment analyses. We sincerely thank the officers and crew of R/V Atlantic Explorer (Bermuda Institute of Ocean Sciences) for their expert assistance on the cruises. The data used in this study are listed in the figures, tables, and references, and are also available in the NSF's Biological and Chemical Oceanography Data Management Office (BCO‐DMO, https://doi.org/10.1575/1912/bco‐dmo.775902.1).
    Description: 2020-02-16
    Keywords: Hurricanes ; Carbon cycle ; North Atlantic Ocean ; Deep ocean ; Particle fluxes ; Lipid biomarkers
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 7
    Publication Date: 2022-10-26
    Description: © The Author(s), 2019. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in DeGrandpre, M. D., Lai, C., Timmermans, M., Krishfield, R. A., Proshutinsky, A., & Torres, D. Inorganic carbon and pCO(2) variability during ice formation in the Beaufort Gyre of the Canada Basin. Journal of Geophysical Research-Oceans, 124(6), (2019): 4017-4028, doi:10.1029/2019JC015109.
    Description: Solute exclusion during sea ice formation is a potentially important contributor to the Arctic Ocean inorganic carbon cycle that could increase as ice cover diminishes. When ice forms, solutes are excluded from the ice matrix, creating a brine that includes dissolved inorganic carbon (DIC) and total alkalinity (AT). The brine sinks, potentially exporting DIC and AT to deeper water. This phenomenon has rarely been observed, however. In this manuscript, we examine a ~1 year pCO2 mooring time series where a ~35‐μatm increase in pCO2 was observed in the mixed layer during the ice formation period, corresponding to a simultaneous increase in salinity from 27.2 to 28.5. Using salinity and ice based mass balances, we show that most of the observed increases can be attributed to solute exclusion during ice formation. The resulting pCO2 is sensitive to the ratio of AT and DIC retained in the ice and the mixed layer depth, which controls dilution of the ice‐derived AT and DIC. In the Canada Basin, of the ~92 μmol/kg increase in DIC, 17 μmol/kg was taken up by biological production and the remainder was trapped between the halocline and the summer stratified surface layer. Although not observed before the mooring was recovered, this inorganic carbon was likely later entrained with surface water, increasing the pCO2 at the surface. It is probable that inorganic carbon exclusion during ice formation will have an increasingly important influence on DIC and pCO2 in the surface of the Arctic Ocean as seasonal ice production and wind‐driven mixing increase with diminishing ice cover.
    Description: Research Associate Cory Beatty (University of Montana) prepared the CO2 instruments and helped with the mooring deployments and data processing. Pierce Fix (undergraduate intern, University of Montana) helped with the mass balance modeling. The moorings were designed and deployed by personnel at Woods Hole Oceanographic Institution. Michiyo Yamamoto‐Kawai (University of Tokyo) and Marty Davelaar (Institute of Ocean Sciences; IOS) provided the alkalinity and dissolved inorganic carbon data. We thank the captain, officers, crew, and chief scientists (Bill Williams and Sarah Zimmerman, IOS) of the CCGS Louis S. St. Laurent. The data used in this study are available through the U.S. National Science Foundation (NSF) Arctic Data Center (https://arcticdata.io). This research was made possible by grants from the NSF Arctic Observing Network program (ARC‐1107346, PLR‐1302884, PLR‐1504410, and PLR‐1723308).
    Keywords: Sea ice ; Dissolved inorganic carbon ; Carbon cycle ; Solute exclusion ; Partial pressure of CO2 ; Arctic Ocean
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 8
    Publication Date: 2022-10-26
    Description: © The Author(s), 2018. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Cael, B. B., & Bisson, K. (2018). Particle flux parameterizations: Quantitative and mechanistic similarities and differences. Frontiers in Marine Science, 5, (2018): 395. doi:10.3389/fmars.2018.00395.
    Description: The depth-attenuation of sinking particulate organic carbon (POC) is of particular importance for the ocean's role in the global carbon cycle. Numerous idealized flux-vs.-depth relationships are available to parameterize this process in Earth System Models. Here we show that these relationships are statistically indistinguishable from available POC flux profile data. Despite their quantitative similarity, we also show these relationships have very different implications for the flux leaving the upper ocean, as well as for the mechanisms governing POC flux. We discuss how this tension might be addressed both observationally and in modeling studies.
    Description: The National Aeronautics and Space Administration supported this work (awards NNX16AR47G and NNX16AR49G).
    Keywords: Carbon export ; Martin curve ; Carbon cycle ; Remineralization depth ; Particulate organic matter
    Repository Name: Woods Hole Open Access Server
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  • 9
    Publication Date: 2022-06-09
    Description: Merapi volcano (Indonesia) is one of the most active and hazardous volcanoes in the world. It is known for frequent small to moderate eruptions, pyroclastic flows produced by lava dome collapse, and the large population settled on and around the flanks of the volcano that is at risk. Its usual behavior for the last decades abruptly changed in late October and early November 2010, when the volcano produced its largest and most explosive eruptions in more than a century, displacing at least a third of a million people, and claiming nearly 400 lives. Despite the challenges involved in forecasting this ‘hundred year eruption’, we show that the magnitude of precursory signals (seismicity, ground deformation, gas emissions) was proportional to the large size and intensity of the eruption. In addition and for the first time, near-real-time satellite radar imagery played an equal role with seismic, geodetic, and gas observations in monitoring eruptive activity during a major volcanic crisis. The Indonesian Center of Volcanology and Geological Hazard Mitigation (CVGHM) issued timely forecasts of the magnitude of the eruption phases, saving 10,000–20,000 lives. In addition to reporting on aspects of the crisis management, we report the first synthesis of scientific observations of the eruption. Our monitoring and petrologic data show that the 2010 eruption was fed by rapid ascent of magma from depths ranging from 5 to 30km. Magma reached the surface with variable gas content resulting in alternating explosive and rapid effusive eruptions, and released a total of ~0.44Tg of SO2. The eruptive behavior seems also related to the seismicity along a tectonic fault more than 40km from the volcano, highlighting both the complex stress pattern of the Merapi region of Java and the role of magmatic pressurization in activating regional faults. We suggest a dynamic triggering of the main explosions on 3 and 4 November by the passing seismic waves generated by regional earthquakes on these days.
    Description: Published
    Description: 121–135
    Description: 5V. Sorveglianza vulcanica ed emergenze
    Description: JCR Journal
    Description: restricted
    Keywords: Merapi ; SAR change detection ; eruption monitoring ; petrology ; satellite monitoring ; volcano tremors ; 04. Solid Earth::04.08. Volcanology::04.08.01. Gases ; 04. Solid Earth::04.08. Volcanology::04.08.03. Magmas ; 04. Solid Earth::04.08. Volcanology::04.08.06. Volcano monitoring ; 04. Solid Earth::04.08. Volcanology::04.08.07. Instruments and techniques
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
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  • 10
    Publication Date: 2022-05-26
    Description: Author Posting. © American Geophysical Union, 2015. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research: Biogeosciences 120 (2015): 379–398, doi:10.1002/2014JG002818.
    Description: A quantitative understanding of the rate at which land ecosystems are sequestering or losing carbon at national-, regional-, and state-level scales is needed to develop policies to mitigate climate change. In this study, a new improved historical land use and land cover change data set is developed and combined with a process-based ecosystem model to estimate carbon sources and sinks in land ecosystems of the conterminous United States for the contemporary period of 2001–2005 and over the last three centuries. We estimate that land ecosystems in the conterminous United States sequestered 323 Tg C yr−1 at the beginning of the 21st century with forests accounting for 97% of this sink. This land carbon sink varied substantially across the conterminous United States, with the largest sinks occurring in the Southeast. Land sinks are large enough to completely compensate fossil fuel emissions in Maine and Mississippi, but nationally, carbon sinks compensate for only 20% of U.S. fossil fuel emissions. We find that regions that are currently large carbon sinks (e.g., Southeast) tend to have been large carbon sources over the longer historical period. Both the land use history and fate of harvested products can be important in determining a region's overall impact on the atmospheric carbon budget. While there are numerous options for reducing fossil fuels (e.g., increase efficiency and displacement by renewable resources), new land management opportunities for sequestering carbon need to be explored. Opportunities include reforestation and managing forest age structure. These opportunities will vary from state to state and over time across the United States.
    Description: This work was supported by NSF grants 104918, 1137306, and 1237491; EPA grant XA-83600001-1; and DOE grant DE-FG02-94ER61937.
    Description: 2015-08-28
    Keywords: Carbon cycle ; Land carbon sinks ; Land use and land cover change ; Stand age ; Fossil fuel emissions ; Land use legacies
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: application/pdf
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