Carbon capture and storage (CCS) provides a solution toward decarbonization of the global economy. The success of this solution depends on the ability to safely and permanently store CO2 This study demonstrates for the first time the permanent disposal of CO2 as environmentally benign carbonate minerals in basaltic rocks. We find that over 95% of the CO2 injected into the CarbFix site in Iceland was mineralized to carbonate minerals in less than 2 years. This result contrasts with the common view that the immobilization of CO2 as carbonate minerals within geologic reservoirs takes several hundreds to thousands of years. Our results, therefore, demonstrate that the safe long-term storage of anthropogenic CO2 emissions through mineralization can be far faster than previously postulated. Copyright © 2016, American Association for the Advancement of Science.

Seasonal field observations show that the North Sea, a Northern European shelf sea, is highly efficient in pumping carbon dioxide from the atmosphere to the North Atlantic Ocean. The bottom topography–controlled stratification separates production and respiration processes in the North Sea, causing a carbon dioxide increase in the subsurface layer that is ultimately exported to the North Atlantic Ocean. Globally extrapolated, the net uptake of carbon dioxide by coastal and marginal seas is about 20% of the world ocean's uptake of anthropogenic carbon dioxide, thus enhancing substantially the open ocean carbon dioxide storage.

An 18-year monitoring record (1978-1995) of dissolved oxygen within a region having hypoxia (dissolved oxygen less than 2 mgl(-1)) in the bottom layer was examined to describe seasonal and annual trends. The monitoring location was near or within a well-described summer hypoxic zone whose size has been up to 20,000 km(2). The monitoring data were used to hindcast the size of the hypoxic zone for before consistent shelfwide surveys started, and to predict it for 1989, when a complete shelfwide survey was not made. The concentration of total Kjeldahl nitrogen (TKN) in surface waters and concentration of bottom water oxygen were directly related, as anticipated if organic loading from surface to bottom was from in situ processes. The TKN data were used to develop a predictive relationship that suggested there was no substantial hypoxia before the 1970s, which was before nitrate flux from the Mississippi River to the Gulf of Mexico began to rise. The peak frequency in monthly hypoxic events is two to three months after both the spring maximum in discharge and nitrate loading of the Mississippi River. These results support the conclusion that persistent, large-sized summer hypoxia is a recently-developed phenomenon that began in the 1970s or early 1980s.

\nFor a majority of aquatic ecosystems, respiration (R)\nexceeds autochthonous gross primary production (GPP). These systems have\nnegative net ecosystem production\n([NEP]=[GPP]–R) and\nratios of [GPP]/R of <1. This net\nheterotrophy can be sustained only if aquatic respiration is subsidized by\norganic inputs from the catchment. Such subsidies imply that organic materials\nthat escaped decomposition in the terrestrial environment must become\nsusceptible to decomposition in the linked aquatic environment.\nUsing a moderate-sized catchment in North America, the Hudson River (catchment\narea 33500 km2), evidence is presented for the magnitude\nof net heterotrophy. All approaches (CO2 gas flux;\nO2 gas flux; budget and gradient of dissolved organic C;\nand the summed components of primary production and respiration within the\necosystem) indicate that system respiration exceeds gross primary production\nby ~200 g C m-2 year-1. Highly\n14C-depleted C of ancient terrestrial origin\n(1000–5000 years old) may be an important source of labile organic\nmatter to this riverine system and support this excess respiration. The\nmechanisms by which organic matter is preserved for centuries to millennia in\nterrestrial soils and decomposed in a matter of weeks in a river connect\nmodern riverine metabolism to historical terrestrial conditions.\n

\n The partial pressure of carbon dioxide (pCO\n 2\n ) in surface waters and related atmospheric exchanges were measured in nine European estuaries. Averaged fluxes over the entire estuaries are usually in the range of 0.1 to 0.5 mole of CO\n 2\n per square meter per day. For wide estuaries, net daily fluxes to the atmosphere amount to several hundred tons of carbon (up to 790 tons of carbon per day in the Scheldt estuary). European estuaries emit between 30 and 60 million tons of carbon per year to the atmosphere, representing 5 to 10% of present anthropogenic CO\n 2\n emissions for Western Europe.\n

Most inverse atmospheric models report considerable uptake of carbon dioxide in Europe's terrestrial biosphere. In contrast, carbon stocks in terrestrial ecosystems increase at a much smaller rate, with carbon gains in forests and grassland soils almost being offset by carbon losses from cropland and peat soils. Accounting for non–carbon dioxide carbon transfers that are not detected by the atmospheric models and for carbon dioxide fluxes bypassing the ecosystem carbon stocks considerably reduces the gap between the small carbon-stock changes and the larger carbon dioxide uptake estimated by atmospheric models. The remaining difference could be because of missing components in the stock-change approach, as well as the large uncertainty in both methods. With the use of the corrected atmosphere- and land-based estimates as a dual constraint, we estimate a net carbon sink between 135 and 205 teragrams per year in Europe's terrestrial biosphere, the equivalent of 7 to 12% of the 1995 anthropogenic carbon emissions.

. Past characterizations of the land–ocean continuum were constructed either from a continental perspective through an analysis of watershed river basin properties (COSCATs: COastal Segmentation and related CATchments) or from an oceanic perspective, through a regionalization of the proximal and distal continental margins (LMEs: large marine ecosystems). Here, we present a global-scale coastal segmentation, composed of three consistent levels, that includes the whole aquatic continuum with its riverine, estuarine and shelf sea components. Our work delineates comprehensive ensembles by harmonizing previous segmentations and typologies in order to retain the most important physical characteristics of both the land and shelf areas. The proposed multi-scale segmentation results in a distribution of global exorheic watersheds, estuaries and continental shelf seas among 45 major zones (MARCATS: MARgins and CATchments Segmentation) and 149 sub-units (COSCATs). Geographic and hydrologic parameters such as the surface area, volume and freshwater residence time are calculated for each coastal unit as well as different hypsometric profiles. Our analysis provides detailed insights into the distributions of coastal and continental shelf areas and how they connect with incoming riverine fluxes. The segmentation is also used to re-evaluate the global estuarine CO2 flux at the air–water interface combining global and regional average emission rates derived from local studies.\n

. The global carbon cycle is part of the much more extensive sedimentary cycle that involves large masses of carbon in the Earth's inner and outer spheres. Studies of the carbon cycle generally followed a progression in knowledge of the natural biological, then chemical, and finally geological processes involved, culminating in a more or less integrated picture of the biogeochemical carbon cycle by the 1920s. However, knowledge of the ocean's carbon cycle behavior has only within the last few decades progressed to a stage where meaningful discussion of carbon processes on an annual to millennial time scale can take place. In geologically older and pre-industrial time, the ocean was generally a net source of CO2 emissions to the atmosphere owing to the mineralization of land-derived organic matter in addition to that produced in situ and to the process of CaCO3 precipitation. Due to rising atmospheric CO2 concentrations because of fossil fuel combustion and land use changes, the direction of the air-sea CO2 flux has reversed, leading to the ocean as a whole being a net sink of anthropogenic CO2. The present thickness of the surface ocean layer, where part of the anthropogenic CO2 emissions are stored, is estimated as of the order of a few hundred meters. The oceanic coastal zone net air-sea CO2 exchange flux has also probably changed during industrial time. Model projections indicate that in pre-industrial times, the coastal zone may have been net heterotrophic, releasing CO2 to the atmosphere from the imbalance between gross photosynthesis and total respiration. This, coupled with extensive CaCO3 precipitation in coastal zone environments, led to a net flux of CO2 out of the system. During industrial time the coastal zone ocean has tended to reverse its trophic status toward a non-steady state situation of net autotrophy, resulting in net uptake of anthropogenic CO2 and storage of carbon in the coastal ocean, despite the significant calcification that still occurs in this region. Furthermore, evidence from the inorganic carbon cycle indicates that deposition and net storage of CaCO3 in sediments exceed inflow of inorganic carbon from land and produce CO2 emissions to the atmosphere. In the shallow-water coastal zone, increase in atmospheric CO2 during the last 300 years of industrial time may have reduced the rate of calcification, and continuation of this trend is an issue of serious environmental concern in the global carbon balance.\n

The battle to reduce greenhouse gas emissions and prevent the most dangerous consequences of climate change will be waged across multiple fronts, including efforts to increase energy efficiency; efforts to deploy nonfossil fuel sources, including renewable and nuclear energy; and investment in adaptation to reduce the impacts of the climate change that will occur regardless of the actions we take. But with more than 80% of the world's energy coming from fossil fuel, winning the battle also requires capturing CO2 from large stationary sources and storing that CO2 in geologic repositories. Offshore geological repositories have received relatively little attention as potential CO2 storage sites, despite their having a number of important advantages over onshore sites, and should be considered more closely.