Monitoring of the gas composition and stable carbon isotopes during side track drilling in Ktzi 203 at the Ketzin CO₂ storage pilot site, Germany

Between 2004 and 2017 the storage of CO2 in a deep saline aquifer was investigated in detail at the Ketzin pilot site close to Berlin. The series of research projects, coordinated by the GFZ German Research Centre for Geosciences, also incorporated an interdisciplinary scientific monitoring program during all phases of the storage process which provided a reliable insight into the overall behaviour of CO2 during storage in the underground.Prior to abandonment and cementing of the Ktzi 203 observation well, two side tracks were cored from 643.1 to 662.6&thinsp;m and from 624.5 to 654.5&thinsp;m, respectively. The drilled sections included the transition zone from the cap rock (Weser Formation) to the reservoir in the Stuttgart Formation which had been exposed to the injected CO2 for more than nine years. During the drilling operation continuous mud gas logging was performed by applying a mud gas separator, a mass spectrometer and a CO2 isotope-analyser for continuous separation and analyses of the extracted gas. Drill cores were shrink-wrapped with plastic foil to collect discharging gases.CO2 concentrations in the cap rock were relatively low and their isotopic compositions were in accord with typical Upper Triassic formation fluids providing no evidence for a significant CO2 infiltration from the underlying reservoir into the cap rock. A clear increase in the CO2 concentration and a shift in δ13CCO2 between the cap rock and the reservoir indicated the presence of the injected CO2 in the sandstone formation. The comparison with samples collected five years earlier in 2012 showed similar concentrations and isotopic depth trends which indicate a rather stagnant CO2 plume at depth and the tightness and integrity of the cap rock and the borehole cementing.</p

Deglacial and Holocene sea-ice and climate dynamics in the Bransfield Strait, northern Antarctic Peninsula

The reconstruction of past sea-ice distribution in the Southern Ocean is crucial for an improved understanding of ice–ocean–atmosphere feedbacks and the evaluation of Earth system and Antarctic ice sheet models. The Antarctic Peninsula (AP) has been experiencing a warming since the start of regular monitoring of the atmospheric temperature in the 1950s. The associated decrease in sea-ice cover contrasts the trend of growing sea-ice extent in East Antarctica. To reveal the long-term sea-ice history at the northern Antarctic Peninsula (NAP) under changing climate conditions, we examined a marine sediment core from the eastern basin of the Bransfield Strait covering the last Deglacial and the Holocene. For sea-ice reconstructions, we focused on the specific sea-ice biomarker lipid IPSO25, a highly branched isoprenoid (HBI), and sea-ice diatoms, whereas a phytoplankton-derived HBI triene (C25:3) and warmer open-ocean diatom assemblages reflect predominantly ice-free conditions. We further reconstruct ocean temperatures using glycerol dialkyl glycerol tetraethers (GDGTs) and diatom assemblages and compare our sea-ice and temperature records with published marine sediment and ice core data. A maximum ice cover is observed during the Antarctic Cold Reversal 13 800–13 000 years before present (13.8–13 ka), while seasonally ice-free conditions permitting (summer) phytoplankton productivity are reconstructed for the late Deglacial and the Early Holocene from 13 to 8.3 ka. An overall decreasing sea-ice trend throughout the Middle Holocene coincides with summer ocean warming and increasing phytoplankton productivity. The Late Holocene is characterized by highly variable winter sea-ice concentrations and a sustained decline in the duration and/or concentration of spring sea ice. Overall diverging trends in GDGT-based TEX86L and RI-OH' subsurface ocean temperatures (SOTs) are found to be linked to opposing spring and summer insolation trends, respectively.</p

Seasonality of Glacial Snow and Ice Microbial Communities

Blooms of microalgae on glaciers and ice sheets are amplifying surface ice melting rates, which are already affected by climate change. Most studies on glacial microorganisms (including snow and glacier ice algae) have so far focused on the spring and summer melt season, leading to a temporal bias, and a knowledge gap in our understanding of the variations in microbial diversity, productivity, and physiology on glacier surfaces year-round. Here, we investigated the microbial communities from Icelandic glacier surface snow and bare ice habitats, with sampling spanning two consecutive years and carried out in both winter and two summer seasons. We evaluated the seasonal differences in microbial community composition using Illumina sequencing of the 16S rRNA, 18S rRNA, and ITS marker genes and correlating them with geochemical signals in the snow and ice. During summer, Chloromonas, Chlainomonas, Raphidonema, and Hydrurus dominated surface snow algal communities, while Ancylonema and Mesotaenium dominated the surface bare ice habitats. In winter, algae could not be detected, and the community composition was dominated by bacteria and fungi. The dominant bacterial taxa found in both winter and summer samples were Bacteriodetes, Actinobacteria, Alphaproteobacteria, and Gammaproteobacteria. The winter bacterial communities showed high similarities to airborne and fresh snow bacteria reported in other studies. This points toward the importance of dry and wet deposition as a wintertime source of microorganisms to the glacier surface. Winter samples were also richer in nutrients than summer samples, except for dissolved organic carbon—which was highest in summer snow and ice samples with blooming microalgae, suggesting that nutrients are accumulated during winter but primarily used by the microbial communities in the summer. Overall, our study shows that glacial snow and ice microbial communities are highly variable on a seasonal basis

Seasonality of Glacial Snow and Ice Microbial Communities.

Blooms of microalgae on glaciers and ice sheets are amplifying surface ice melting rates, which are already affected by climate change. Most studies on glacial microorganisms (including snow and glacier ice algae) have so far focused on the spring and summer melt season, leading to a temporal bias, and a knowledge gap in our understanding of the variations in microbial diversity, productivity, and physiology on glacier surfaces year-round. Here, we investigated the microbial communities from Icelandic glacier surface snow and bare ice habitats, with sampling spanning two consecutive years and carried out in both winter and two summer seasons. We evaluated the seasonal differences in microbial community composition using Illumina sequencing of the 16S rRNA, 18S rRNA, and ITS marker genes and correlating them with geochemical signals in the snow and ice. During summer, Chloromonas, Chlainomonas, Raphidonema, and Hydrurus dominated surface snow algal communities, while Ancylonema and Mesotaenium dominated the surface bare ice habitats. In winter, algae could not be detected, and the community composition was dominated by bacteria and fungi. The dominant bacterial taxa found in both winter and summer samples were Bacteriodetes, Actinobacteria, Alphaproteobacteria, and Gammaproteobacteria. The winter bacterial communities showed high similarities to airborne and fresh snow bacteria reported in other studies. This points toward the importance of dry and wet deposition as a wintertime source of microorganisms to the glacier surface. Winter samples were also richer in nutrients than summer samples, except for dissolved organic carbon-which was highest in summer snow and ice samples with blooming microalgae, suggesting that nutrients are accumulated during winter but primarily used by the microbial communities in the summer. Overall, our study shows that glacial snow and ice microbial communities are highly variable on a seasonal basis

Preservation of organic carbon during active fluvial transport and particle abrasion

Oxidation of particulate organic carbon (POC) during fluvial transit releases CO2 to the atmosphere and can influence global climate. Field data show large POC oxidation fluxes in lowland rivers; however, it is unclear if POC losses occur predominantly during in-river transport, where POC is in continual motion within an aerated environment, or during transient storage in floodplains, which may be anoxic. Determination of the locus of POC oxidation in lowland rivers is needed to develop process-based models to predict POC losses, constrain carbon budgets, and unravel links between climate and erosion. However, sediment exchange between rivers and floodplains makes differentiating POC oxidation during in-river transport from oxidation during floodplain storage difficult. Here, we isolated in-river POC oxidation using flume experiments transporting petrogenic and biospheric POC without floodplain storage. Our experiments showed solid phase POC losses of 0%–10% over ~103 km of fluvial transport, compared to ~7% to >50% losses observed in rivers over similar distances. The production of dissolved organic carbon (DOC) and dissolved rhenium (a proxy for petrogenic POC oxidation) was consistent with small POC losses, and replicate experiments in static water tanks gave similar results. Our results show that fluvial sediment transport, particle abrasion, and turbulent mixing have a minimal role on POC oxidation, and they suggest that POC losses may accrue primarily in floodplain storage

Insight Into Hartoušov Mofette, Czech Republic: Tales by the Fluids

The Cheb Basin (Czech Republic) is characterized by emanations of magma-derived gases and repeated occurrences of mid-crustal earthquake swarms with small to intermediate magnitudes (ML < 4.5). Associated intense mantle degassing occurs at the Hartoušov Mofette, a representative site for the Cheb Basin. Here, we performed 14 sampling campaigns between June 2019 and March 2020. Gas samples of fluids ascending in two boreholes (F1, ∼28 m depth and F2, ∼108 m depth) and from a nearby natural mofette were analyzed for their chemical (CO2, N2, O2, Ar, He, CH4, and H2) and isotope compositions (noble gases and CO2). CO2 concentrations were above 99.1% in most samples, while O2 and N2 were below 0.6%. He ranged from 19 to 34 μmol/mol and CH4 was mostly below 12 μmol/mol. Isotope compositions of helium and carbon in CO2 ranged from 5.39 to 5.86 RA and from −2.4 to −1.3 ‰ versus VPDB, respectively. Solubility differences of the investigated gases resulted in fluctuations of their chemical compositions. These differences were accompanied by observed changes of gas fluxes in the field and at the monitoring station for F1. Variations in solubilities and fluxes also impacted the chemical concentration of the gases and the δ13C values that were also likely influenced by Fischer-Tropsch type reactions. The combination of (a) the Bernard ratio, (b) CH4/3He distributions, (c) P-T conditions, (d) heat flow, and (e) the sedimentary regime led to the hypothesis that CH4 may be of mixed biogenic and volcanic/geothermal origin with a noticeable atmospheric contribution. The drilling of a third borehole (F3) with a depth of ∼238 m in August 2019 has been crucial for providing insights into the complex system of Hartoušov Mofette

Mobilization of optically invisible dissolved organic matter in response to rainstorm events in a tropical forest headwater river

This study emphasizes the importance of rainstorm events in mobilizing carbon at the soil‐stream interface from tropical rainforests. Half‐hourly geochemical/isotopic records over a 13.5 h period from a 20 km2 tropical rainforest headwater in Guyana show an order of magnitude increase in dissolved organic carbon (DOC) concentration in less than 30 mins (10.6–114 mg/L). The composition of DOC varies significantly and includes optically invisible dissolved organic matter (iDOM) that accounts for a large proportion (4–89%) of the total DOC, quantified using size exclusion chromatography (SEC). SEC suggests that iDOM is comprised of low molecular weight organic moieties, which are likely sourced from fresh leaf litter and/or topsoil, as shown in soils from the surrounding environment. Although poorly constrained at present, the presence of iDOM further downstream during the wet season suggests that this organic matter fraction may represent an unquantified source of riverine CO2 outgassing in tropical headwaters, requiring further consideration