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R.M. Key

Bio: R.M. Key is an academic researcher from Princeton University. The author has contributed to research in topics: World Ocean Circulation Experiment & Global Ocean Data Analysis Project. The author has an hindex of 9, co-authored 11 publications receiving 3852 citations.

Papers
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Journal ArticleDOI
16 Jul 2004-Science
TL;DR: Using inorganic carbon measurements from an international survey effort in the 1990s and a tracer-based separation technique, the authors estimate a global oceanic anthropogenic carbon dioxide (CO2) sink for the period from 1800 to 1994 of 118 19 petagrams of carbon.
Abstract: Using inorganic carbon measurements from an international survey effort in the 1990s and a tracer-based separation technique, we estimate a global oceanic anthropogenic carbon dioxide (CO2) sink for the period from 1800 to 1994 of 118 19 petagrams of carbon. The oceanic sink accounts for48% of the total fossil-fuel and cement-manufacturing emissions, implying that the terrestrial biosphere was a net source of CO 2 to the atmosphere of about 39 28 petagrams of carbon for this period. The current fraction of total anthropogenic CO2 emissions stored in the ocean appears to be about one-third of the long-term potential. Since the beginning of the industrial period in the late 18th century, i.e., over the anthropocene (1), humankind has emitted large quantities of CO2 into the atmosphere, mainly as a result of fossil-fuel burning, but also because of land-use practices, e.g., deforestation (2). Measurements and reconstructions of the atmospheric CO2 history reveal, however, that less than half of these emissions remain in the atmosphere (3). The anthropogenic CO2 that did not accumulate in the atmosphere must have been taken up by the ocean, by the land biosphere, or by a combination of both. The relative roles of the ocean and land biosphere as sinks for anthropogenic CO2 over the anthropocene are currently not known. Although the anthropogenic CO2 budget for the past two decades, i.e., the 1980s and 1990s, has been investigated in detail (3), the estimates of the ocean sink have not been based on direct measurements of changes in the oceanic inventory of dissolved inorganic carbon (DIC). Recognizing the need to constrain the oceanic uptake, transport, and storage of anthropogenic CO 2 for the anthropocene and to provide a baseline for future estimates of oceanic CO 2 uptake, two international ocean research programs, the World Ocean Circulation Experiment (WOCE) and the Joint Global Ocean Flux Study (JGOFS), jointly conducted a comprehensive survey of inorganic carbon distributions in the global ocean in the 1990s (4). After completion of the U.S. field program in 1998, a 5-year effort was begun to compile and rigorously quality-control the U.S. and international data sets, in

3,291 citations

Journal ArticleDOI
TL;DR: This paper used the most complete database of dissolved inorganic radiocarbon, DI14C, available to date and a suite of ocean general circulation models in an inverse mode to recalculate the ocean inventory of bomb-produced DI 14C in the global ocean.
Abstract: [1] The 14CO2 released into the stratosphere during bomb testing in the early 1960s provides a global constraint on air-sea gas exchange of soluble atmospheric gases like CO2. Using the most complete database of dissolved inorganic radiocarbon, DI14C, available to date and a suite of ocean general circulation models in an inverse mode we recalculate the ocean inventory of bomb-produced DI14C in the global ocean and confirm that there is a 25% decrease from previous estimates using older DI14C data sets. Additionally, we find a 33% lower globally averaged gas transfer velocity for CO2 compared to previous estimates (Wanninkhof, 1992) using the NCEP/NCAR Reanalysis 1 1954–2000 where the global mean winds are 6.9 m s−1. Unlike some earlier ocean radiocarbon studies, the implied gas transfer velocity finally closes the gap between small-scale deliberate tracer studies and global-scale estimates. Additionally, the total inventory of bomb-produced radiocarbon in the ocean is now in agreement with global budgets based on radiocarbon measurements made in the stratosphere and troposphere. Using the implied relationship between wind speed and gas transfer velocity ks = 0.27〈u102〉(Sc/660)−0.5 and standard partial pressure difference climatology of CO2 we obtain an net air-sea flux estimate of 1.3 ± 0.5 PgCyr−1 for 1995. After accounting for the carbon transferred from rivers to the deep ocean, our estimate of oceanic uptake (1.8 ± 0.5 PgCyr−1) compares well with estimates based on ocean inventories, ocean transport inversions using ocean concentration data, and model simulations.

497 citations

Journal ArticleDOI
TL;DR: The GLODAPv2 data product as discussed by the authors is composed of data from 724 scientific cruises covering the global ocean and includes data from an additional 168 cruises, including data from CARINA (CARbon IN the Atlantic) in 2009/2010, and PACIFICA (PACIFic ocean interior CArbon) in 2013, as well as data from a total of 724 cruises.
Abstract: . Version 2 of the Global Ocean Data Analysis Project (GLODAPv2) data product is composed of data from 724 scientific cruises covering the global ocean. It includes data assembled during the previous efforts GLODAPv1.1 (Global Ocean Data Analysis Project version 1.1) in 2004, CARINA (CARbon IN the Atlantic) in 2009/2010, and PACIFICA (PACIFic ocean Interior CArbon) in 2013, as well as data from an additional 168 cruises. Data for 12 core variables (salinity, oxygen, nitrate, silicate, phosphate, dissolved inorganic carbon, total alkalinity, pH, CFC-11, CFC-12, CFC-113, and CCl4) have been subjected to extensive quality control, including systematic evaluation of bias. The data are available in two formats: (i) as submitted but updated to WOCE exchange format and (ii) as a merged and internally consistent data product. In the latter, adjustments have been applied to remove significant biases, respecting occurrences of any known or likely time trends or variations. Adjustments applied by previous efforts were re-evaluated. Hence, GLODAPv2 is not a simple merging of previous products with some new data added but a unique, internally consistent data product. This compiled and adjusted data product is believed to be consistent to better than 0.005 in salinity, 1 % in oxygen, 2 % in nitrate, 2 % in silicate, 2 % in phosphate, 4 µmol kg−1 in dissolved inorganic carbon, 6 µmol kg−1 in total alkalinity, 0.005 in pH, and 5 % for the halogenated transient tracers. The original data and their documentation and doi codes are available at the Carbon Dioxide Information Analysis Center ( http://cdiac.ornl.gov/oceans/GLODAPv2/ ). This site also provides access to the calibrated data product, which is provided as a single global file or four regional ones – the Arctic, Atlantic, Indian, and Pacific oceans – under the doi:10.3334/CDIAC/OTG.NDP093_GLODAPv2 . The product files also include significant ancillary and approximated data. These were obtained by interpolation of, or calculation from, measured data. This paper documents the GLODAPv2 methods and products and includes a broad overview of the secondary quality control results. The magnitude of and reasoning behind each adjustment is available on a per-cruise and per-variable basis in the online Adjustment Table.

415 citations

DOI
14 Dec 2015
TL;DR: The Global Ocean Data Analysis Project version 2 (GLODAPv2) as discussed by the authors is a uniformly calibrated open ocean data product on inorganic carbon and carbon-relevant variables that includes data from approximately one million individual seawater samples collected from over 700 cruises during the years 1972-2013.
Abstract: Here we report the completion of a uniformly calibrated open ocean data product on inorganic carbon and carbon-relevant variables that we call Global Ocean Data Analysis Project version 2 or simply GLODAPv2. The product includes data from approximately one million individual seawater samples collected from over 700 cruises during the years 1972-2013. Extensive quality control and subsequent calibration were carried out for salinity, oxygen, nutrient, carbon dioxide, total alkalinity, pH and chlorofluorocarbon data. Following calibration, the data were used to produce global climatology maps for many of the parameters. In addition to the data products and the mapped distributions, all of the original data files without alteration other than formatting and unification of units are made freely available along with whatever metadata was collected. An on-line cruise summary table provides data access and additional information including references to publications that have used data from specific cruises. The GLODAPv2 database is available free of charge as a numeric data package (NDP-93) from the Carbon Dioxide Information Analysis Center (CDIAC) at http://cdiac.ornl.gov/oceans/GLODAPv2/. The NDP-93 consists of the original cruise data files, adjusted data products, mapped data product and this documentation, which describes the GLODAPv2 project.

102 citations

Journal ArticleDOI
TL;DR: In this article, the authors describe the steps taken for quality controlling chosen parameters within the Arctic Ocean data included in the CARINA data set and checking for offsets between the individual cruises.
Abstract: . The paper describes the steps taken for quality controlling chosen parameters within the Arctic Ocean data included in the CARINA data set and checking for offsets between the individual cruises. The evaluated parameters are the inorganic carbon parameters (total dissolved inorganic carbon, total alkalinity and pH), oxygen and nutrients: nitrate, phosphate and silicate. More parameters can be found in the CARINA data product, but were not subject to a secondary quality control. The main method in determining offsets between cruises was regional multi-linear regression, after a first rough basin-wide deep-water estimate of each parameter. Lastly, the results of the secondary quality control are discussed as well as applied adjustments.

30 citations


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TL;DR: In this article, the authors proposed a new approach to global sustainability in which they define planetary boundaries within which they expect that humanity can operate safely. But the proposed concept of "planetary boundaries" lays the groundwork for shifting our approach to governance and management, away from the essentially sectoral analyses of limits to growth aimed at minimizing negative externalities, toward the estimation of the safe space for human development.
Abstract: Anthropogenic pressures on the Earth System have reached a scale where abrupt global environmental change can no longer be excluded. We propose a new approach to global sustainability in which we define planetary boundaries within which we expect that humanity can operate safely. Transgressing one or more planetary boundaries may be deleterious or even catastrophic due to the risk of crossing thresholds that will trigger non-linear, abrupt environmental change within continental- to planetary-scale systems. We have identified nine planetary boundaries and, drawing upon current scientific understanding, we propose quantifications for seven of them. These seven are climate change (CO2 concentration in the atmosphere <350 ppm and/or a maximum change of +1 W m-2 in radiative forcing); ocean acidification (mean surface seawater saturation state with respect to aragonite ≥ 80% of pre-industrial levels); stratospheric ozone (<5% reduction in O3 concentration from pre-industrial level of 290 Dobson Units); biogeochemical nitrogen (N) cycle (limit industrial and agricultural fixation of N2 to 35 Tg N yr-1) and phosphorus (P) cycle (annual P inflow to oceans not to exceed 10 times the natural background weathering of P); global freshwater use (<4000 km3 yr-1 of consumptive use of runoff resources); land system change (<15% of the ice-free land surface under cropland); and the rate at which biological diversity is lost (annual rate of <10 extinctions per million species). The two additional planetary boundaries for which we have not yet been able to determine a boundary level are chemical pollution and atmospheric aerosol loading. We estimate that humanity has already transgressed three planetary boundaries: for climate change, rate of biodiversity loss, and changes to the global nitrogen cycle. Planetary boundaries are interdependent, because transgressing one may both shift the position of other boundaries or cause them to be transgressed. The social impacts of transgressing boundaries will be a function of the social-ecological resilience of the affected societies. Our proposed boundaries are rough, first estimates only, surrounded by large uncertainties and knowledge gaps. Filling these gaps will require major advancements in Earth System and resilience science. The proposed concept of "planetary boundaries" lays the groundwork for shifting our approach to governance and management, away from the essentially sectoral analyses of limits to growth aimed at minimizing negative externalities, toward the estimation of the safe space for human development. Planetary boundaries define, as it were, the boundaries of the "planetary playing field" for humanity if we want to be sure of avoiding major human-induced environmental change on a global scale.

4,771 citations

Journal ArticleDOI
29 Sep 2005-Nature
TL;DR: 13 models of the ocean–carbon cycle are used to assess calcium carbonate saturation under the IS92a ‘business-as-usual’ scenario for future emissions of anthropogenic carbon dioxide and indicate that conditions detrimental to high-latitude ecosystems could develop within decades, not centuries as suggested previously.
Abstract: Today's surface ocean is saturated with respect to calcium carbonate, but increasing atmospheric carbon dioxide concentrations are reducing ocean pH and carbonate ion concentrations, and thus the level of calcium carbonate saturation. Experimental evidence suggests that if these trends continue, key marine organisms—such as corals and some plankton—will have difficulty maintaining their external calcium carbonate skeletons. Here we use 13 models of the ocean–carbon cycle to assess calcium carbonate saturation under the IS92a 'business-as-usual' scenario for future emissions of anthropogenic carbon dioxide. In our projections, Southern Ocean surface waters will begin to become undersaturated with respect to aragonite, a metastable form of calcium carbonate, by the year 2050. By 2100, this undersaturation could extend throughout the entire Southern Ocean and into the subarctic Pacific Ocean. When live pteropods were exposed to our predicted level of undersaturation during a two-day shipboard experiment, their aragonite shells showed notable dissolution. Our findings indicate that conditions detrimental to high-latitude ecosystems could develop within decades, not centuries as suggested previously.

4,244 citations

Journal ArticleDOI
TL;DR: The potential for marine organisms to adapt to increasing CO2 and broader implications for ocean ecosystems are not well known; both are high priorities for future research as mentioned in this paper, and both are only imperfect analogs to current conditions.
Abstract: Rising atmospheric carbon dioxide (CO2), primarily from human fossil fuel combustion, reduces ocean pH and causes wholesale shifts in seawater carbonate chemistry. The process of ocean acidification is well documented in field data, and the rate will accelerate over this century unless future CO2 emissions are curbed dramatically. Acidification alters seawater chemical speciation and biogeochemical cycles of many elements and compounds. One well-known effect is the lowering of calcium carbonate saturation states, which impacts shell-forming marine organisms from plankton to benthic molluscs, echinoderms, and corals. Many calcifying species exhibit reduced calcification and growth rates in laboratory experiments under high-CO2 conditions. Ocean acidification also causes an increase in carbon fixation rates in some photosynthetic organisms (both calcifying and noncalcifying). The potential for marine organisms to adapt to increasing CO2 and broader implications for ocean ecosystems are not well known; both are high priorities for future research. Although ocean pH has varied in the geological past, paleo-events may be only imperfect analogs to current conditions.

2,995 citations

Journal ArticleDOI
TL;DR: In this paper, the authors identify key areas of uncertainty and specific actions needed to address them and identify the value of mangrove forests, seagrass beds, and salt marshes in sequestering carbon dioxide.
Abstract: Recent research has highlighted the valuable role that coastal and marine ecosystems play in sequestering carbon dioxide (CO(2)). The carbon (C) sequestered in vegetated coastal ecosystems, specifically mangrove forests, seagrass beds, and salt marshes, has been termed blue carbon. Although their global area is one to two orders of magnitude smaller than that of terrestrial forests, the contribution of vegetated coastal habitats per unit area to long-term C sequestration is much greater, in part because of their efficiency in trapping suspended matter and associated organic C during tidal inundation. Despite the value of mangrove forests, seagrass beds, and salt marshes in sequestering C, and the other goods and services they provide, these systems are being lost at critical rates and action is urgently needed to prevent further degradation and loss. Recognition of the C sequestration value of vegetated coastal ecosystems provides a strong argument for their protection and restoration; however, it is necessary to improve scientific understanding of the underlying mechanisms that control C sequestration in these ecosystems. Here, we identify key areas of uncertainty and specific actions needed to address them.

2,313 citations

Journal ArticleDOI
TL;DR: The relationship between temperature and individual performance is reasonably well understood, and much climate-related research has focused on potential shifts in distribution and abundance driven directly by temperature as discussed by the authors, however, recent work has revealed that both abiotic changes and biological responses in the ocean will be substantially more complex.
Abstract: Anthropogenically induced global climate change has profound implications for marine ecosystems and the economic and social systems that depend upon them. The relationship between temperature and individual performance is reasonably well understood, and much climate-related research has focused on potential shifts in distribution and abundance driven directly by temperature. However, recent work has revealed that both abiotic changes and biological responses in the ocean will be substantially more complex. For example, changes in ocean chemistry may be more important than changes in temperature for the performance and survival of many organisms. Ocean circulation, which drives larval transport, will also change, with important consequences for population dynamics. Furthermore, climatic impacts on one or a few 'leverage species' may result in sweeping community-level changes. Finally, synergistic effects between climate and other anthropogenic variables, particularly fishing pressure, will likely exacerbate climate-induced changes. Efforts to manage and conserve living marine systems in the face of climate change will require improvements to the existing predictive framework. Key directions for future research include identifying key demographic transitions that influence population dynamics, predicting changes in the community-level impacts of ecologically dominant species, incorporating populations' ability to evolve (adapt), and understanding the scales over which climate will change and living systems will respond.

2,137 citations