Description: Highlights • Approaches for CO2 leakage detection, attribution and quantification monitoring exist. • Many approaches cover multiple monitoring tasks simultaneously. • Sonars and chemical sensors on ships or AUVs can cover large areas. • Newer, more specific technologies can detect, verify and quantify smaller, localised leaks. Environmental monitoring of offshore Carbon Capture and Storage (CCS) complexes requires robust methodologies and cost-effective tools to detect, attribute and quantify CO2 leakage in the unlikely event it occurs from a sub-seafloor reservoir. Various approaches can be utilised for environmental CCS monitoring, but their capabilities are often undemonstrated and more detailed monitoring strategies need to be developed. We tested and compared different approaches in an offshore setting using a CO2 release experiment conducted at 120 m water depth in the Central North Sea. Tests were carried out over a range of CO2 injection rates (6 - 143 kg d−1) comparable to emission rates observed from abandoned wells. Here, we discuss the benefits and challenges of the tested approaches and compare their relative cost, temporal and spatial resolution, technology readiness level and sensitivity to leakage. The individual approaches demonstrate a high level of sensitivity and certainty and cover a wide range of operational requirements. Additionally, we refer to a set of generic requirements for site-specific baseline surveys that will aid in the interpretation of the results. Critically, we show that the capability of most techniques to detect and quantify leakage exceeds the currently existing legal requirements.

Description: Highlights • Surface sediments react quickly with leaking CO2 and release cations into porewaters. • Both carbonate and silicate mineral dissolution lead to neutralization of CO2 in the sediments. • During short-term exposure to CO2 no toxic substances were released from North Sea surface sediments. • Porewater composition can be used as a diagnostic indicator of CO2 leakage from storage reservoirs. Abstract Sub-seabed geological CO2 storage is discussed as a climate mitigation strategy, but the impact of any leakage of stored CO2 into the marine environment is not well known. In this study, leakage from a CO2 storage reservoir through near-surface sediments was mimicked for low leakage rates in the North Sea. Field data were combined with laboratory experiments and transport-reaction modelling to estimate CO2 and mineral dissolution rates, and to assess the mobilization of metals in contact with CO2-rich fluids and their potential impact on the environment. We found that carbonate and silicate minerals reacted quickly with the dissolved CO2, increasing porewater alkalinity and neutralizing about 5% of the injected CO2. The release of Ca, Sr, Ba and Mn was mainly controlled by carbonate dissolution, while Fe, Li, B, Mg, and Si were released from silicate minerals, mainly from deeper sediment layers. No toxic metals were released from the sediments and overall the injected CO2 was only detected up to 1 m away from seabed CO2 bubble streams. Our results suggest that low leakage rates of CO2 over short timescales have minimal impact on the benthic environment. However, porewater composition and temperature are effective indicators for leakage detection, even at low CO2 leakage rates.

Description: Highlights • In-situ temperature measurements were conducted at the Danube deep sea fan. • Operations were performed with the MARUM-MeBo200 seafloor drill rig. • The BSR is located ∼20 m below the current gas hydrate stability zone. • Seismic data suggest presence of shallower BSR-like events. Abstract Coring, geophysical logging, and in-situ temperature measurements were performed with the MARUM-MeBo200 seafloor rig to characterize gas hydrate occurrences in sediments of the Danube deep sea fan, off Romania, Black Sea. The new drilling data showed no evidence for significant gas hydrate saturations within the sediments but the presence of free gas at the depth of the bottom-simulating reflector (BSR). In-situ temperature and core-derived geochemical data suggest that the current base of the gas hydrate stability zone (BGHSZ) is ∼20 m shallower than the BSR. Investigation of the seismic data around the drill sites shows several locations where free gas previously trapped at a former BGHSZ migrated upwards forming a new reflection above the BSR. This shows that the gas hydrate system in the Danube deep sea fan is still responding to climate changes initiated at the end of the last glacial maximum.

Description: Highlights • Geochemical analyses highlight multiple diagenesis processes occurring in the sediment. • Intense methane seepages and organic matter degradation contribute to the sulfate reduction. • Chemical of dissolved and mineral iron species indicate that iron is associated with clay minerals. • In response to seawater intrusion, ion exchange, dissolution and reverse weathering reactions change the composition of clay constituting the sediment. Abstract Pore water and sediment geochemistry in the western Black Sea were investigated on long Calypso piston core samples. Using this type of coring device facilitates the recovery of the thick sediment record necessary to analyze transport-reaction processes in response to the postglacial sea-level rise and intrusion of Mediterranean salt water 9 ka ago, and thus, to better characterize key biogeochemical processes and process changes in response to the shift from lacustrine to marine bottom water composition. Complementary data indicate that organic matter degradation occurs in the upper 15 m of the sediment column. However, sulfate reduction coupled with Anaerobic Methane Oxidation (AOM) is the dominant electron-accepting process and characterized by a shallow Sulfate Methane Transition Zone (SMTZ). Net silica dissolution, total alkalinity (TA) maxima and carbonate peaks are found at shallow depths. Pore water profiles clearly show the uptake of K+, Mg2+ and Na + by, and release of Ca2+ and Sr2+ from the heterogeneous lacustrine sediments, which is likely controlled by chemical reactions of silicate minerals and changes in clay mineral composition. Iron (Fe2+) and manganese (Mn2+) maxima largely coincide with Ca2+ peaks and suggest a close link between Fe2+, Mn2+ and Ca2+ release. We hypothesize that the Fe2+ maxima below the SMTZ result from deep Fe3+ reduction linked to organic matter degradation, either driven by DOC escaping from the shallow sulfate reduction zone or slow degradation of recalcitrant POC. The chemical analysis of dissolved and solid iron species indicates that iron is essentially associated with clay minerals, which suggests that microbial iron reduction is influenced by clay mineral composition and bioavailability of clay mineral-bound Fe(III). Overall, our study suggests that postglacial seawater intrusion plays a major role in shaping redox zonation and geochemical profiles in the lacustrine sediments of the Late Quaternary.

Description: Carbon capture and storage (CCS) is a key technology to reduce carbon dioxide (CO2) emissions from industrial processes in a feasible, substantial, and timely manner. For geological CO2 storage to be safe, reliable, and accepted by society, robust strategies for CO2 leakage detection, quantification and management are crucial. The STEMM-CCS (Strategies for Environmental Monitoring of Marine Carbon Capture and Storage) project aimed to provide techniques and understanding to enable and inform cost-effective monitoring of CCS sites in the marine environment. A controlled CO2 release experiment was carried out in the central North Sea, designed to mimic an unintended emission of CO2 from a subsurface CO2 storage site to the seafloor. A total of 675 kg of CO2 were released into the shallow sediments (~3 m 49 below seafloor), at flow rates between 6 and 143 kg/d. A combination of novel techniques, adapted versions of existing techniques, and well-proven standard techniques were used to detect, characterise and quantify gaseous and dissolved CO2 in the sediments and the overlying seawater. This paper provides an overview of this ambitious field experiment. We describe the preparatory work prior to the release experiment, the experimental layout and procedures, the methods tested, and summarise the main results and the lessons learnt.

Description: Evaluation of seismic reflection data has identified the presence of fluid escape structures cross-cutting overburden stratigraphy within sedimentary basins globally. Seismically-imaged chimneys/pipes are considered to be possible pathways for fluid flow, which may hydraulically connect deeper strata to the seabed. These fluid migration pathways through the overburden must be constrained to enable secure, long-term subsurface carbon dioxide (CO2) storage. We have investigated a site of natural active fluid escape in the North Sea, the Scanner Pockmark Complex, to determine the physical characteristics of focused fluid conduits, and how they control fluid flow. Here we show that a multi-scale, multi disciplinary experimental approach is required for complete characterisation of fluid escape structures. Geophysical techniques are necessary to resolve fracture geometry and subsurface structure (e.g., multifrequency seismics) and physical parameters of sediments (e.g., controlled source electromagnetics) across length scales (m to km). At smaller (mm to cm) scales, sediment cores were sampled directly and their physical and chemical properties assessed using laboratory-based methods. Numerical modelling approaches bridge the resolution gap, though their validity is dependent on calibration and constraint from field and laboratory experimental data. Further, time-lapse seismic and acoustic methods capable of resolving temporal changes are key for determining fluid flux. Future optimisation of experiment resource use may be facilitated by the installation of permanent seabed infrastructure, and replacement of manual data processing with automated workflows. This study can be used to inform measurement, monitoring and verification workflows that will assist policymaking, regulation, and best practice for CO2 subsurface storage operations.

Description: Highlights • A biogeochemical baseline of sediment geochemistry at potential offshore CCS sites. • Diagnostic indicators of CO2 leakage based on stoichiometry of porewater chemistry. • Porewater chemistry is modified by reverse weathering processes at Goldeneye site. Abstract Injection of carbon dioxide (CO2) into subseafloor reservoirs is gaining traction as a strategy for mitigating anthropogenic CO2 emissions to the atmosphere. Yet, potential leakage, migration and dissolution of externally-supplied CO2 from such reservoirs are a cause for concern. The potential impact of CO2 leakage on the biogeochemistry of sediments and overlying waters in the North Sea was studied during a controlled subsurface CO2 release experiment in 2019 at a potential carbon capture and storage site (Goldeneye). This study describes the natural (unperturbed) biogeochemistry of sediments. They are classified as muddy sand to sandy mud with low organic carbon content (∼0.6 %). Distributions of dissolved inorganic carbon (DIC) and total alkalinity (TA) in sediment porewaters are reported in addition to in situ benthic fluxes of dissolved nutrients and oxygen between the sediments and the overlying water. Oxygen fluxes into the sediment, measured using benthic chambers and eddy covariance, were 6.18 ± 0.58 and 5.73 ± 2.03 mmol m−2 d-1, respectively. Diagnostic indicators are discussed that could be used to detect CO2 enrichment of sediments due to reservoir leakage at CCS sites. These include the ratio TA and ammonium to sulfate in sediment porewaters, benthic fluxes and chloride-normalized cation distributions. These indicators currently suggest that the organic carbon at Goldeneye has an oxidation state below zero and is mainly degraded via sulfate reduction. Carbonate precipitation is apparently negligible, whereas decreases in Mg2+ and K+ point toward ongoing alteration of lithogenic sediments by reverse weathering processes.

Description: Highlights • Four seafloor hydrocarbon emissions in the Eastern Black Sea were investigated • Eocene and/or Oligocene-Miocene Formations are most likely sources for oil and gas • Mixed secondary microbial and oil-associated thermogenic hydrocarbons at all sites • Site-specific light hydrocarbon compositions result from different mixing ratios Abstract Numerous hydrocarbon seep sites at the continental shelf, slope, and in the deep water basin are known to feed the Black Sea water reservoir of dissolved methane. In this study, we identified the likely sources of gas and oil that are emitted at four sites located on the continental slope offshore Georgia in the Eastern Black Sea at 830 to 1,140 m water depth – an area with gas seepage only (Batumi seep area) and three areas of joint gas and oil seepage (Iberia Mound, Colkheti Seep, and Pechori Mound). The geochemistry of bulk parameters, organic fractions and individual hydrocarbon biomarkers in near-surface sediments and of gas/oil expelled from the seafloor was analyzed and jointly interpreted to assign most likely hydrocarbon source rocks in the studied region. Presence of oleanane in shallow oil-impregnated sediments and oil slicks attests that the source rock at all sites is younger than Mid Cretaceous in age. We conclude that hydrocarbons ascending at all the four seepage areas originate from the Eocene Kuma Formation and/or the Oligocene–Lower Miocene Maikop Group, which are considered the principal hydrocarbon sources in the Eastern Black Sea region. Distributions of crude oil biomarkers in shallow sediments suggests moderate to heavy biodegradation. C1/C2+ ratios (10 to 4,163) along with stable C and H isotopic ratios (δ13C-CH4 ‒46.3 to ‒53.1.3‰ V-PDB; δ2H-CH4 ‒159 to ‒178‰ SMOW) indicate gas mixtures of oil-associated thermogenic and secondary microbial light hydrocarbons that are discharged from the four seep sites. Light hydrocarbons discharged at the Batumi Seep area are characterized by significant enrichments of methane, but almost similar δ13C-CH4 values if compared to the other study sites. Such methane enrichments likely result from a comparably higher degree of petroleum degradation and associated formation of secondary microbial methane.