Najjar
Raymond G.
Najjar
Raymond G.
No Thumbnail Available
12 results
Search Results
Now showing
1 - 12 of 12
-
ArticleCarbon cycling in the North American coastal ocean: a synthesis(European Geosciences Union, 2019-03-27) Fennel, Katja ; Alin, Simone R. ; Barbero, Leticia ; Evans, Wiley ; Bourgeois, Timothée ; Cooley, Sarah R. ; Dunne, John P. ; Feely, Richard A. ; Hernandez-Ayon, Jose Martin ; Hu, Xinping ; Lohrenz, Steven E. ; Muller-Karger, Frank E. ; Najjar, Raymond G. ; Robbins, Lisa ; Shadwick, Elizabeth H. ; Siedlecki, Samantha A. ; Steiner, Nadja ; Sutton, Adrienne J. ; Turk, Daniela ; Vlahos, Penny ; Wang, Zhaohui AleckA quantification of carbon fluxes in the coastal ocean and across its boundaries with the atmosphere, land, and the open ocean is important for assessing the current state and projecting future trends in ocean carbon uptake and coastal ocean acidification, but this is currently a missing component of global carbon budgeting. This synthesis reviews recent progress in characterizing these carbon fluxes for the North American coastal ocean. Several observing networks and high-resolution regional models are now available. Recent efforts have focused primarily on quantifying the net air–sea exchange of carbon dioxide (CO2). Some studies have estimated other key fluxes, such as the exchange of organic and inorganic carbon between shelves and the open ocean. Available estimates of air–sea CO2 flux, informed by more than a decade of observations, indicate that the North American Exclusive Economic Zone (EEZ) acts as a sink of 160±80 Tg C yr−1, although this flux is not well constrained. The Arctic and sub-Arctic, mid-latitude Atlantic, and mid-latitude Pacific portions of the EEZ account for 104, 62, and −3.7 Tg C yr−1, respectively, while making up 51 %, 25 %, and 24 % of the total area, respectively. Combining the net uptake of 160±80 Tg C yr−1 with an estimated carbon input from land of 106±30 Tg C yr−1 minus an estimated burial of 65±55 Tg C yr−1 and an estimated accumulation of dissolved carbon in EEZ waters of 50±25 Tg C yr−1 implies a carbon export of 151±105 Tg C yr−1 to the open ocean. The increasing concentration of inorganic carbon in coastal and open-ocean waters leads to ocean acidification. As a result, conditions favoring the dissolution of calcium carbonate occur regularly in subsurface coastal waters in the Arctic, which are naturally prone to low pH, and the North Pacific, where upwelling of deep, carbon-rich waters has intensified. Expanded monitoring and extension of existing model capabilities are required to provide more reliable coastal carbon budgets, projections of future states of the coastal ocean, and quantification of anthropogenic carbon contributions.
-
ArticleA modeling study of the seasonal oxygen budget of the global ocean(American Geophysical Union, 2007-05-09) Jin, X. ; Najjar, Raymond G. ; Louanchi, F. ; Doney, Scott C.An ecosystem model embedded in a global ocean general circulation model is used to quantify roles of biological and physical processes on seasonal oxygen variations. We find that the thermally induced seasonal net outgassing (SNO) of oxygen is overestimated by about 30% if gas phase equilibrium is assumed, and we find that seasonal variations in thermocline oxygen due to biology are approximated well using the oxygen anomaly. Outside the tropics and the north Indian Ocean, biological SNO is, on average, 56% of net community production (defined as net oxygen production above 76 m) during the outgassing period and 35% of annual net community production. In the same region the seasonal drawdown of the oxygen anomaly within the upper thermocline (76–500 m) is 76% of the remineralization during the drawdown and 48% of annual remineralization. Applying model-derived relationships to observed O2 climatologies and using independent estimates for tropical and monsoonal systems, we estimate global net community production to be 14.9 ± 2.5 Pg C yr−1.
-
ArticleSurface ocean pCO2 seasonality and sea-air CO2 flux estimates for the North American east coast(John Wiley & Sons, 2013-10-16) Signorini, Sergio R. ; Mannino, Antonio ; Najjar, Raymond G. ; Friedrichs, Marjorie A. M. ; Cai, Wei-Jun ; Salisbury, Joseph E. ; Wang, Zhaohui Aleck ; Thomas, Helmuth ; Shadwick, Elizabeth H.Underway and in situ observations of surface ocean pCO2, combined with satellite data, were used to develop pCO2 regional algorithms to analyze the seasonal and interannual variability of surface ocean pCO2 and sea-air CO2 flux for five physically and biologically distinct regions of the eastern North American continental shelf: the South Atlantic Bight (SAB), the Mid-Atlantic Bight (MAB), the Gulf of Maine (GoM), Nantucket Shoals and Georges Bank (NS+GB), and the Scotian Shelf (SS). Temperature and dissolved inorganic carbon variability are the most influential factors driving the seasonality of pCO2. Estimates of the sea-air CO2 flux were derived from the available pCO2 data, as well as from the pCO2 reconstructed by the algorithm. Two different gas exchange parameterizations were used. The SS, GB+NS, MAB, and SAB regions are net sinks of atmospheric CO2 while the GoM is a weak source. The estimates vary depending on the use of surface ocean pCO2 from the data or algorithm, as well as with the use of the two different gas exchange parameterizations. Most of the regional estimates are in general agreement with previous studies when the range of uncertainty and interannual variability are taken into account. According to the algorithm, the average annual uptake of atmospheric CO2 by eastern North American continental shelf waters is found to be between −3.4 and −5.4 Tg C yr−1 (areal average of −0.7 to −1.0 mol CO2 m−2 yr−1) over the period 2003–2010.
-
Working PaperA science plan for carbon cycle research in North American coastal waters. Report of the Coastal CARbon Synthesis (CCARS) community workshop, August 19-21, 2014(Ocean Carbon & Biogeochemistry Program, 2016) Benway, Heather M. ; Alin, Simone R. ; Boyer, Elizabeth ; Cai, Wei-Jun ; Coble, Paula G. ; Cross, Jessica N. ; Friedrichs, Marjorie A. M. ; Goni, Miguel ; Griffith, Peter C. ; Herrmann, Maria ; Lohrenz, Steven E. ; Mathis, Jeremy T. ; McKinley, Galen A. ; Najjar, Raymond G. ; Pilskaln, Cynthia H. ; Siedlecki, Samantha A. ; Smith, Richard A.Relative to their surface area, continental margins represent some of the largest carbon fluxes in the global ocean, but sparse and sporadic sampling in space and time makes these systems difficult to characterize and quantify. Recognizing the importance of continental margins to the overall North American carbon budget, terrestrial and marine carbon cycle scientists have been collaborating on a series of synthesis, carbon budgeting, and modeling exercises for coastal regions of North America, which include the Gulf of Mexico, the Laurentian Great Lakes (LGL), and the coastal waters of the Atlantic, Pacific, and Arctic Oceans. The Coastal CARbon Synthesis (CCARS) workshops and research activities have been conducted over the past several years as a partner activity between the Ocean Carbon and Biogeochemistry (OCB) Program and the North American Carbon Program (NACP) to synthesize existing data and improve quantitative assessments of the North American carbon budget.
-
PreprintAnthropogenic ocean acidification over the twenty-first century and its impact on calcifying organisms( 2005-07-29) Orr, James C. ; Fabry, Victoria J. ; Aumont, Olivier ; Bopp, Laurent ; Doney, Scott C. ; Feely, Richard A. ; Gnanadesikan, Anand ; Gruber, Nicolas ; Ishida, Akio ; Joos, Fortunat ; Key, Robert M. ; Lindsay, Keith ; Maier-Reimer, Ernst ; Matear, Richard J. ; Monfray, Patrick ; Mouchet, Anne ; Najjar, Raymond G. ; Plattner, Gian-Kasper ; Rodgers, Keith B. ; Sabine, Christopher L. ; Sarmiento, Jorge L. ; Schlitzer, Reiner ; Slater, Richard D. ; Totterdell, Ian J. ; Weirig, Marie-France ; Yamanaka, Yasuhiro ; Yool, AndrewThe surface ocean is everywhere saturated with respect to calcium carbonate (CaCO3). Yet increasing atmospheric CO2 reduces ocean pH and carbonate ion concentrations [CO32−] and thus the level of saturation. Reduced saturation states are expected to affect marine calcifiers even though it has been estimated that all surface waters will remain saturated for centuries. Here we show, however, that some surface waters will become undersaturated within decades. When atmospheric CO2 reaches 550 ppmv, in year 2050 under the IS92a business-as-usual scenario, Southern Ocean surface waters begin to become undersaturated with respect to aragonite, a metastable form of CaCO3. By 2100 as atmospheric CO2 reaches 788 ppmv, undersaturation extends throughout the entire Southern Ocean (< 60°S) and into the subarctic Pacific. These changes will threaten high-latitude aragonite secreting organisms including cold-water corals, which provide essential fish habitat, and shelled pteropods, an abundant food source for marine predators.
-
ArticleBiogeochemical protocols and diagnostics for the CMIP6 Ocean Model Intercomparison Project (OMIP)(Copernicus Publications on behalf of the European Geosciences Union, 2017-06-09) Orr, James C. ; Najjar, Raymond G. ; Aumont, Olivier ; Bopp, Laurent ; Bullister, John L. ; Danabasoglu, Gokhan ; Doney, Scott C. ; Dunne, John P. ; Dutay, Jean-Claude ; Graven, Heather ; Griffies, Stephen M. ; John, Jasmin G. ; Joos, Fortunat ; Levin, Ingeborg ; Lindsay, Keith ; Matear, Richard J. ; McKinley, Galen A. ; Mouchet, Anne ; Oschlies, Andreas ; Romanou, Anastasia ; Schlitzer, Reiner ; Tagliabue, Alessandro ; Tanhua, Toste ; Yool, AndrewThe Ocean Model Intercomparison Project (OMIP) focuses on the physics and biogeochemistry of the ocean component of Earth system models participating in the sixth phase of the Coupled Model Intercomparison Project (CMIP6). OMIP aims to provide standard protocols and diagnostics for ocean models, while offering a forum to promote their common assessment and improvement. It also offers to compare solutions of the same ocean models when forced with reanalysis data (OMIP simulations) vs. when integrated within fully coupled Earth system models (CMIP6). Here we detail simulation protocols and diagnostics for OMIP's biogeochemical and inert chemical tracers. These passive-tracer simulations will be coupled to ocean circulation models, initialized with observational data or output from a model spin-up, and forced by repeating the 1948–2009 surface fluxes of heat, fresh water, and momentum. These so-called OMIP-BGC simulations include three inert chemical tracers (CFC-11, CFC-12, SF6) and biogeochemical tracers (e.g., dissolved inorganic carbon, carbon isotopes, alkalinity, nutrients, and oxygen). Modelers will use their preferred prognostic BGC model but should follow common guidelines for gas exchange and carbonate chemistry. Simulations include both natural and total carbon tracers. The required forced simulation (omip1) will be initialized with gridded observational climatologies. An optional forced simulation (omip1-spunup) will be initialized instead with BGC fields from a long model spin-up, preferably for 2000 years or more, and forced by repeating the same 62-year meteorological forcing. That optional run will also include abiotic tracers of total dissolved inorganic carbon and radiocarbon, CTabio and 14CTabio, to assess deep-ocean ventilation and distinguish the role of physics vs. biology. These simulations will be forced by observed atmospheric histories of the three inert gases and CO2 as well as carbon isotope ratios of CO2. OMIP-BGC simulation protocols are founded on those from previous phases of the Ocean Carbon-Cycle Model Intercomparison Project. They have been merged and updated to reflect improvements concerning gas exchange, carbonate chemistry, and new data for initial conditions and atmospheric gas histories. Code is provided to facilitate their implementation.
-
ArticleEvaluation of ocean carbon cycle models with data-based metrics(American Geophysical Union, 2004-04-02) Matsumoto, K. ; Sarmiento, Jorge L. ; Key, Robert M. ; Aumont, Olivier ; Bullister, John L. ; Caldeira, Ken ; Campin, J.-M. ; Doney, Scott C. ; Drange, Helge ; Dutay, J.-C. ; Follows, Michael J. ; Gao, Y. ; Gnanadesikan, Anand ; Gruber, Nicolas ; Ishida, Akio ; Joos, Fortunat ; Lindsay, Keith ; Maier-Reimer, Ernst ; Marshall, John C. ; Matear, Richard J. ; Monfray, Patrick ; Mouchet, Anne ; Najjar, Raymond G. ; Plattner, Gian-Kasper ; Schlitzer, Reiner ; Slater, Richard D. ; Swathi, P. S. ; Totterdell, Ian J. ; Weirig, Marie-France ; Yamanaka, Yasuhiro ; Yool, Andrew ; Orr, James C.New radiocarbon and chlorofluorocarbon-11 data from the World Ocean Circulation Experiment are used to assess a suite of 19 ocean carbon cycle models. We use the distributions and inventories of these tracers as quantitative metrics of model skill and find that only about a quarter of the suite is consistent with the new data-based metrics. This should serve as a warning bell to the larger community that not all is well with current generation of ocean carbon cycle models. At the same time, this highlights the danger in simply using the available models to represent the state-of-the-art modeling without considering the credibility of each model.
-
ArticleEvaluating global ocean carbon models : the importance of realistic physics(American Geophysical Union, 2004-09-15) Doney, Scott C. ; Lindsay, Keith ; Caldeira, Ken ; Campin, J.-M. ; Drange, Helge ; Dutay, J.-C. ; Follows, Michael J. ; Gao, Y. ; Gnanadesikan, Anand ; Gruber, Nicolas ; Ishida, Akio ; Joos, Fortunat ; Madec, G. ; Maier-Reimer, Ernst ; Marshall, John C. ; Matear, Richard J. ; Monfray, Patrick ; Mouchet, Anne ; Najjar, Raymond G. ; Orr, James C. ; Plattner, Gian-Kasper ; Sarmiento, Jorge L. ; Schlitzer, Reiner ; Slater, Richard D. ; Totterdell, Ian J. ; Weirig, Marie-France ; Yamanaka, Yasuhiro ; Yool, AndrewA suite of standard ocean hydrographic and circulation metrics are applied to the equilibrium physical solutions from 13 global carbon models participating in phase 2 of the Ocean Carbon-cycle Model Intercomparison Project (OCMIP-2). Model-data comparisons are presented for sea surface temperature and salinity, seasonal mixed layer depth, meridional heat and freshwater transport, 3-D hydrographic fields, and meridional overturning. Considerable variation exists among the OCMIP-2 simulations, with some of the solutions falling noticeably outside available observational constraints. For some cases, model-model and model-data differences can be related to variations in surface forcing, subgrid-scale parameterizations, and model architecture. These errors in the physical metrics point to significant problems in the underlying model representations of ocean transport and dynamics, problems that directly affect the OCMIP predicted ocean tracer and carbon cycle variables (e.g., air-sea CO2 flux, chlorofluorocarbon and anthropogenic CO2 uptake, and export production). A substantial fraction of the large model-model ranges in OCMIP-2 biogeochemical fields (±25–40%) represents the propagation of known errors in model physics. Therefore the model-model spread likely overstates the uncertainty in our current understanding of the ocean carbon system, particularly for transport-dominated fields such as the historical uptake of anthropogenic CO2. A full error assessment, however, would need to account for additional sources of uncertainty such as more complex biological-chemical-physical interactions, biases arising from poorly resolved or neglected physical processes, and climate change.
-
ArticleCarbon budget of tidal wetlands, estuaries, and shelf waters of eastern North America(John Wiley & Sons, 2018-04-04) Najjar, Raymond G. ; Herrmann, Maria ; Alexander, Richard ; Boyer, Elizabeth W. ; Burdige, David J. ; Butman, David ; Cai, Wei-Jun ; Canuel, Elizabeth A. ; Chen, Robert F. ; Friedrichs, Marjorie A. M. ; Feagin, Russell A. ; Griffith, Peter C. ; Hinson, Audra L. ; Holmquist, James R. ; Hu, Xinping ; Kemp, William M. ; Kroeger, Kevin D. ; Mannino, Antonio ; McCallister, S. Leigh ; McGillis, Wade R. ; Mulholland, Margaret R. ; Pilskaln, Cynthia H. ; Salisbury, Joseph E. ; Signorini, Sergio R. ; St-Laurent, Pierre ; Tian, Hanqin ; Tzortziou, Maria ; Vlahos, Penny ; Wang, Zhaohui Aleck ; Zimmerman, Richard C.Carbon cycling in the coastal zone affects global carbon budgets and is critical for understanding the urgent issues of hypoxia, acidification, and tidal wetland loss. However, there are no regional carbon budgets spanning the three main ecosystems in coastal waters: tidal wetlands, estuaries, and shelf waters. Here we construct such a budget for eastern North America using historical data, empirical models, remote sensing algorithms, and process‐based models. Considering the net fluxes of total carbon at the domain boundaries, 59 ± 12% (± 2 standard errors) of the carbon entering is from rivers and 41 ± 12% is from the atmosphere, while 80 ± 9% of the carbon leaving is exported to the open ocean and 20 ± 9% is buried. Net lateral carbon transfers between the three main ecosystem types are comparable to fluxes at the domain boundaries. Each ecosystem type contributes substantially to exchange with the atmosphere, with CO2 uptake split evenly between tidal wetlands and shelf waters, and estuarine CO2 outgassing offsetting half of the uptake. Similarly, burial is about equal in tidal wetlands and shelf waters, while estuaries play a smaller but still substantial role. The importance of tidal wetlands and estuaries in the overall budget is remarkable given that they, respectively, make up only 2.4 and 8.9% of the study domain area. This study shows that coastal carbon budgets should explicitly include tidal wetlands, estuaries, shelf waters, and the linkages between them; ignoring any of them may produce a biased picture of coastal carbon cycling.
-
ArticleAssessing phytoplankton nutritional status and potential impact of wet deposition in seasonally oligotrophic waters of the Mid‐Atlantic Bight(John Wiley & Sons, 2018-04-06) Sedwick, Peter N. ; Bernhardt, Peter W. ; Mulholland, Margaret R. ; Najjar, Raymond G. ; Blumen, L. M. ; Sohst, Bettina M. ; Sookhdeo, C. ; Widner, BrittanyTo assess phytoplankton nutritional status in seasonally oligotrophic waters of the southern Mid‐Atlantic Bight, and the potential for rain to stimulate primary production in this region during summer, shipboard bioassay experiments were performed using natural seawater and phytoplankton collected north and south of the Gulf Stream. Bioassay treatments comprised iron, nitrate, iron + nitrate, iron + nitrate + phosphate, and rainwater. Phytoplankton growth was inferred from changes in chlorophyll a, inorganic nitrogen, and carbon‐13 uptake, relative to unamended control treatments. Results indicated the greatest growth stimulation by iron + nitrate + phosphate, intermediate growth stimulation by rainwater, modest growth stimulation by nitrate and iron + nitrate, and no growth stimulation by iron. Based on these data and analysis of seawater and atmospheric samples, nitrogen was the proximate limiting nutrient, with a secondary limitation imposed by phosphorus. Our results imply that summer rain events increase new production in these waters by contributing nitrogen and phosphorus, with the availability of the latter setting the upper limit on rain‐stimulated new production.
-
ArticleImpact of circulation on export production, dissolved organic matter, and dissolved oxygen in the ocean : results from Phase II of the Ocean Carbon-cycle Model Intercomparison Project (OCMIP-2)(American Geophysical Union, 2007-08-08) Najjar, Raymond G. ; Jin, X. ; Louanchi, F. ; Aumont, Olivier ; Caldeira, Ken ; Doney, Scott C. ; Dutay, J.-C. ; Follows, Michael J. ; Gruber, Nicolas ; Joos, Fortunat ; Lindsay, Keith ; Maier-Reimer, Ernst ; Matear, Richard J. ; Matsumoto, K. ; Monfray, Patrick ; Mouchet, Anne ; Orr, James C. ; Plattner, Gian-Kasper ; Sarmiento, Jorge L. ; Schlitzer, Reiner ; Slater, Richard D. ; Weirig, Marie-France ; Yamanaka, Yasuhiro ; Yool, AndrewResults are presented of export production, dissolved organic matter (DOM) and dissolved oxygen simulated by 12 global ocean models participating in the second phase of the Ocean Carbon-cycle Model Intercomparison Project. A common, simple biogeochemical model is utilized in different coarse-resolution ocean circulation models. The model mean (±1σ) downward flux of organic matter across 75 m depth is 17 ± 6 Pg C yr−1. Model means of globally averaged particle export, the fraction of total export in dissolved form, surface semilabile dissolved organic carbon (DOC), and seasonal net outgassing (SNO) of oxygen are in good agreement with observation-based estimates, but particle export and surface DOC are too high in the tropics. There is a high sensitivity of the results to circulation, as evidenced by (1) the correlation of surface DOC and export with circulation metrics, including chlorofluorocarbon inventory and deep-ocean radiocarbon, (2) very large intermodel differences in Southern Ocean export, and (3) greater export production, fraction of export as DOM, and SNO in models with explicit mixed layer physics. However, deep-ocean oxygen, which varies widely among the models, is poorly correlated with other model indices. Cross-model means of several biogeochemical metrics show better agreement with observation-based estimates when restricted to those models that best simulate deep-ocean radiocarbon. Overall, the results emphasize the importance of physical processes in marine biogeochemical modeling and suggest that the development of circulation models can be accelerated by evaluating them with marine biogeochemical metrics.
-
ArticleA synthesis of global coastal ocean greenhouse gas fluxes(American Geophysical Union, 2024-01-20) Resplandy, Laure ; Hogikyan, Allison ; Muller, Jens Daniel ; Najjar, Raymond G. ; Bange, Hermann W. ; Bianchi, Daniele ; Weber, Thomas ; Cai, Wei-Jun ; Doney, Scott C. ; Fennel, Katja ; Gehlen, Marion ; Hauck, Judith ; Lacroix, Fabrice ; Landschutzer, Peter ; Le Quere, Corinne ; Roobaert, Alizee ; Schwinger, Jorg ; Berthet, Sarah ; Bopp, Laurent ; Chau, Thi Tuyet Trang ; Dai, Minhan ; Gruber, Nicolas ; Ilyina, Tatiana ; Kock, Annette ; Manizza, Manfredi ; Lachkar, Zouhair ; Laruelle, Goulven G. ; Liao, Enhui ; Lima, Ivan D. ; Nissen, Cara ; Rodenbeck, Christian ; Seferian, Roland ; Toyama, Katsuya ; Tsujino, Hiroyuki ; Regnier, PierreThe coastal ocean contributes to regulating atmospheric greenhouse gas concentrations by taking up carbon dioxide (CO2) and releasing nitrous oxide (N2O) and methane (CH4). In this second phase of the Regional Carbon Cycle Assessment and Processes (RECCAP2), we quantify global coastal ocean fluxes of CO2, N2O and CH4 using an ensemble of global gap-filled observation-based products and ocean biogeochemical models. The global coastal ocean is a net sink of CO2 in both observational products and models, but the magnitude of the median net global coastal uptake is ∼60% larger in models (−0.72 vs. −0.44 PgC year−1, 1998–2018, coastal ocean extending to 300 km offshore or 1,000 m isobath with area of 77 million km2). We attribute most of this model-product difference to the seasonality in sea surface CO2 partial pressure at mid- and high-latitudes, where models simulate stronger winter CO2 uptake. The coastal ocean CO2 sink has increased in the past decades but the available time-resolving observation-based products and models show large discrepancies in the magnitude of this increase. The global coastal ocean is a major source of N2O (+0.70 PgCO2-e year−1 in observational product and +0.54 PgCO2-e year−1 in model median) and CH4 (+0.21 PgCO2-e year−1 in observational product), which offsets a substantial proportion of the coastal CO2 uptake in the net radiative balance (30%–60% in CO2-equivalents), highlighting the importance of considering the three greenhouse gases when examining the influence of the coastal ocean on climate.