Feely Richard A.

Last Name

Feely

First Name

Richard A.

Full item page

Search Results

Now showing 1 - 20 of 24

Carbon 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 Aleck

A 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.
Air-sea CO2 exchange in the equatorial Pacific

(American Geophysical Union, 2004-08-28) McGillis, Wade R. ; Edson, James B. ; Zappa, Christopher J. ; Ware, Jonathan D. ; McKenna, Sean P. ; Terray, Eugene A. ; Hare, Jeffrey E. ; Fairall, Christopher W. ; Drennan, William M. ; Donelan, Mark A. ; DeGrandpre, Michael D. ; Wanninkhof, Rik ; Feely, Richard A.

GasEx-2001, a 15-day air-sea carbon dioxide (CO2) exchange study conducted in the equatorial Pacific, used a combination of ships, buoys, and drifters equipped with ocean and atmospheric sensors to assess variability and surface mechanisms controlling air-sea CO2 fluxes. Direct covariance and profile method air-sea CO2 fluxes were measured together with the surface ocean and marine boundary layer processes. The study took place in February 2001 near 125°W, 3°S in a region of high CO2. The diurnal variation in the air-sea CO2 difference was 2.5%, driven predominantly by temperature effects on surface solubility. The wind speed was 6.0 ± 1.3 m s−1, and the atmospheric boundary layer was unstable with conditions over the range −1 < z/L < 0. Diurnal heat fluxes generated daytime surface ocean stratification and subsequent large nighttime buoyancy fluxes. The average CO2 flux from the ocean to the atmosphere was determined to be 3.9 mol m−2 yr−1, with nighttime CO2 fluxes increasing by 40% over daytime values because of a strong nighttime increase in (vertical) convective velocities. The 15 days of air-sea flux measurements taken during GasEx-2001 demonstrate some of the systematic environmental trends of the eastern equatorial Pacific Ocean. The fact that other physical processes, in addition to wind, were observed to control the rate of CO2 transfer from the ocean to the atmosphere indicates that these processes need to be taken into account in local and global biogeochemical models. These local processes can vary on regional and global scales. The GasEx-2001 results show a weak wind dependence but a strong variability in processes governed by the diurnal heating cycle. This implies that any changes in the incident radiation, including atmospheric cloud dynamics, phytoplankton biomass, and surface ocean stratification may have significant feedbacks on the amount and variability of air-sea gas exchange. This is in sharp contrast with previous field studies of air-sea gas exchange, which showed that wind was the dominating forcing function. The results suggest that gas transfer parameterizations that rely solely on wind will be insufficient for regions with low to intermediate winds and strong insolation.
Comment on “Modern-age buildup of CO2 and its effects on seawater acidity and salinity” by Hugo A. Loáiciga

(American Geophysical Union, 2007-09-25) Caldeira, Ken ; Archer, David ; Barry, James P. ; Bellerby, Richard G. J. ; Brewer, Peter G. ; Cao, Long ; Dickson, Andrew G. ; Doney, Scott C. ; Elderfield, Henry ; Fabry, Victoria J. ; Feely, Richard A. ; Gattuso, Jean-Pierre ; Haugan, Peter M. ; Hoegh-Guldberg, Ove ; Jain, Atul K. ; Kleypas, Joan A. ; Langdon, Chris ; Orr, James C. ; Ridgwell, Andy ; Sabine, Christopher L. ; Seibel, Brad A. ; Shirayama, Yoshihisa ; Turley, Carol ; Watson, Andrew J. ; Zeebe, Richard E.
The impact of the North Atlantic Oscillation on the uptake and accumulation of anthropogenic CO2 by North Atlantic Ocean mode waters

(American Geophysical Union, 2011-09-21) Levine, Naomi M. ; Doney, Scott C. ; Lima, Ivan D. ; Wanninkhof, Rik ; Bates, Nicholas R. ; Feely, Richard A.

The North Atlantic Ocean accounts for about 25% of the global oceanic anthropogenic carbon sink. This basin experiences significant interannual variability primarily driven by the North Atlantic Oscillation (NAO). A suite of biogeochemical model simulations is used to analyze the impact of interannual variability on the uptake and storage of contemporary and anthropogenic carbon (Canthro) in the North Atlantic Ocean. Greater winter mixing during positive NAO years results in increased mode water formation and subsequent increases in subtropical and subpolar Canthro inventories. Our analysis suggests that changes in mode water Canthro inventories are primarily due to changes in water mass volumes driven by variations in water mass transformation rates rather than local air-sea CO2 exchange. This suggests that a significant portion of anthropogenic carbon found in the ocean interior may be derived from surface waters advected into water formation regions rather than from local gas exchange. Therefore, changes in climate modes, such as the NAO, may alter the residence time of anthropogenic carbon in the ocean by altering the rate of water mass transformation. In addition, interannual variability in Canthro storage increases the difficulty of Canthro detection and attribution through hydrographic observations, which are limited by sparse sampling of subsurface waters in time and space.
Comparison of CO2 dynamics and air-sea exchange in differing tropical reef environments

( 2013-01-17) Drupp, Patrick S. ; De Carlo, Eric H. ; Mackenzie, Fred T. ; Sabine, Christopher L. ; Feely, Richard A. ; Shamberger, Kathryn E. F.

An array of MAPCO2 buoys, CRIMP-2, Ala Wai, and Kilo Nalu, deployed in the coastal waters of Hawaii have produced multiyear high temporal resolution CO2 records in three different coral reef environments off the island of Oahu, Hawaii. This study, which includes data from June 2008-December 2011, is part of an integrated effort to understand the factors that influence the dynamics of CO2-carbonic acid system parameters in waters surrounding Pacific high island coral reef ecosystems and subject to differing natural and anthropogenic stresses. The MAPCO2 buoys are located on the Kaneohe Bay backreef, and fringing reef sites on the south shore of O’ahu, Hawai’i. The buoys measure CO2 and O2 in seawater and in the atmosphere at 3-hour intervals, as well as other physical and biogeochemical parameters (CTD, chlorophyll-a, turbidity). The buoy records, combined with data from synoptic spatial sampling, have allowed us to examine the interplay between biological cycles of productivity/respiration and calcification/dissolution and biogeochemical and physical forcings on hourly to inter-annual time scales. Air-sea CO2 gas exchange was also calculated to determine if the locations were sources or sinks of CO2 over seasonal, annual, and interannual time periods. Net annualized fluxes for CRIMP-2, Ala Wai, and Kilo Nalu over the entire study period were 1.15 mol C m-2 yr-1, 0.045 mol C m-2 yr-1, and -0.0056 mol C m-2 yr-1, respectively, where positive values indicate a source or a CO2 flux from the water to the atmosphere, and negative values indicate a sink or flux of CO2 from the atmosphere into the water. These values are of similar magnitude to previous estimates in Kaneohe Bay as well as those reported from other tropical reef environments. Total alkalinity (AT) was measured in conjunction with pCO2 and the carbonic acid system was calculated to compare with other reef systems and open ocean values around Hawaii. These findings emphasize the need for high-resolution data of multiple parameters when attempting to characterize the carbonic-acid system in locations of highly variable physical, chemical, and biological parameters (e.g. coastal systems, reefs).
Using present-day observations to detect when anthropogenic change forces surface ocean carbonate chemistry outside preindustrial bounds

(Copernicus Publications on behalf of the European Geosciences Union, 2016-09-13) Sutton, Adrienne J. ; Sabine, Chris L. ; Feely, Richard A. ; Cai, Wei-Jun ; Cronin, Meghan F. ; McPhaden, Michael J. ; Morell, Julio M. ; Newton, Jan A. ; Noh, Jae Hoon ; Ólafsdóttir, Sólveig R. ; Salisbury, Joseph E. ; Send, Uwe ; Vandemark, Douglas ; Weller, Robert A.

One of the major challenges to assessing the impact of ocean acidification on marine life is detecting and interpreting long-term change in the context of natural variability. This study addresses this need through a global synthesis of monthly pH and aragonite saturation state (Ωarag) climatologies for 12 open ocean, coastal, and coral reef locations using 3-hourly moored observations of surface seawater partial pressure of CO2 and pH collected together since as early as 2010. Mooring observations suggest open ocean subtropical and subarctic sites experience present-day surface pH and Ωarag conditions outside the bounds of preindustrial variability throughout most, if not all, of the year. In general, coastal mooring sites experience more natural variability and thus, more overlap with preindustrial conditions; however, present-day Ωarag conditions surpass biologically relevant thresholds associated with ocean acidification impacts on Mytilus californianus (Ωarag < 1.8) and Crassostrea gigas (Ωarag < 2.0) larvae in the California Current Ecosystem (CCE) and Mya arenaria larvae in the Gulf of Maine (Ωarag < 1.6). At the most variable mooring locations in coastal systems of the CCE, subseasonal conditions approached Ωarag =  1. Global and regional models and data syntheses of ship-based observations tended to underestimate seasonal variability compared to mooring observations. Efforts such as this to characterize all patterns of pH and Ωarag variability and change at key locations are fundamental to assessing present-day biological impacts of ocean acidification, further improving experimental design to interrogate organism response under real-world conditions, and improving predictive models and vulnerability assessments seeking to quantify the broader impacts of ocean acidification.
Global Oceans [in “State of the Climate in 2020”]

(American Meteorological Society, 2021-08-01) Johnson, Gregory C. ; Lumpkin, Rick ; Alin, Simone R. ; Amaya, Dillon J. ; Baringer, Molly O. ; Boyer, Tim ; Brandt, Peter ; Carter, Brendan ; Cetinić, Ivona ; Chambers, Don P. ; Cheng, Lijing ; Collins, Andrew U. ; Cosca, Cathy ; Domingues, Ricardo ; Dong, Shenfu ; Feely, Richard A. ; Frajka-Williams, Eleanor E. ; Franz, Bryan A. ; Gilson, John ; Goni, Gustavo J. ; Hamlington, Benjamin D. ; Herrford, Josefine ; Hu, Zeng-Zhen ; Huang, Boyin ; Ishii, Masayoshi ; Jevrejeva, Svetlana ; Kennedy, John J. ; Kersalé, Marion ; Killick, Rachel E. ; Landschützer, Peter ; Lankhorst, Matthias ; Leuliette, Eric ; Locarnini, Ricardo ; Lyman, John ; Marra, John F. ; Meinen, Christopher S. ; Merrifield, Mark ; Mitchum, Gary ; Moat, Bengamin I. ; Nerem, R. Steven ; Perez, Renellys ; Purkey, Sarah G. ; Reagan, James ; Sanchez-Franks, Alejandra ; Scannell, Hillary A. ; Schmid, Claudia ; Scott, Joel P. ; Siegel, David A. ; Smeed, David A. ; Stackhouse, Paul W. ; Sweet, William V. ; Thompson, Philip R. ; Trinanes, Joaquin ; Volkov, Denis L. ; Wanninkhof, Rik ; Weller, Robert A. ; Wen, Caihong ; Westberry, Toby K. ; Widlansky, Matthew J. ; Wilber, Anne C. ; Yu, Lisan ; Zhang, Huai-Min

This chapter details 2020 global patterns in select observed oceanic physical, chemical, and biological variables relative to long-term climatologies, their differences between 2020 and 2019, and puts 2020 observations in the context of the historical record. In this overview we address a few of the highlights, first in haiku, then paragraph form: La Niña arrives, shifts winds, rain, heat, salt, carbon: Pacific—beyond. Global ocean conditions in 2020 reflected a transition from an El Niño in 2018–19 to a La Niña in late 2020. Pacific trade winds strengthened in 2020 relative to 2019, driving anomalously westward Pacific equatorial surface currents. Sea surface temperatures (SSTs), upper ocean heat content, and sea surface height all fell in the eastern tropical Pacific and rose in the western tropical Pacific. Efflux of carbon dioxide from ocean to atmosphere was larger than average across much of the equatorial Pacific, and both chlorophyll-a and phytoplankton carbon concentrations were elevated across the tropical Pacific. Less rain fell and more water evaporated in the western equatorial Pacific, consonant with increased sea surface salinity (SSS) there. SSS may also have increased as a result of anomalously westward surface currents advecting salty water from the east. El Niño–Southern Oscillation conditions have global ramifications that reverberate throughout the report.
Global ocean carbon uptake : magnitude, variability and trends

(Copernicus Publications on behalf of the European Geosciences Union, 2013-03-22) Wanninkhof, Rik ; Park, Geun-Ha ; Takahashi, Taro ; Sweeney, Colm ; Feely, Richard A. ; Nojiri, Yukihiro ; Gruber, Nicolas ; Doney, Scott C. ; McKinley, Galen A. ; Lenton, Andrew ; Le Quere, Corinne ; Heinze, Christoph ; Schwinger, Jorg ; Graven, Heather ; Khatiwala, Samar

The globally integrated sea–air anthropogenic carbon dioxide (CO2) flux from 1990 to 2009 is determined from models and data-based approaches as part of the Regional Carbon Cycle Assessment and Processes (RECCAP) project. Numerical methods include ocean inverse models, atmospheric inverse models, and ocean general circulation models with parameterized biogeochemistry (OBGCMs). The median value of different approaches shows good agreement in average uptake. The best estimate of anthropogenic CO2 uptake for the time period based on a compilation of approaches is −2.0 Pg C yr−1. The interannual variability in the sea–air flux is largely driven by large-scale climate re-organizations and is estimated at 0.2 Pg C yr−1 for the two decades with some systematic differences between approaches. The largest differences between approaches are seen in the decadal trends. The trends range from −0.13 (Pg C yr−1) decade−1 to −0.50 (Pg C yr−1) decade−1 for the two decades under investigation. The OBGCMs and the data-based sea–air CO2 flux estimates show appreciably smaller decadal trends than estimates based on changes in carbon inventory suggesting that methods capable of resolving shorter timescales are showing a slowing of the rate of ocean CO2 uptake. RECCAP model outputs for five decades show similar differences in trends between approaches.
Air-sea CO2 flux in the Pacific Ocean for the period 1990–2009

(Copernicus Publications on behalf of the European Geosciences Union, 2014-02-06) Ishii, Masao ; Feely, Richard A. ; Rodgers, Keith B. ; Park, Geun-Ha ; Wanninkhof, Rik ; Sasano, D. ; Sugimoto, H. ; Cosca, Catherine E. ; Nakaoka, Shin-ichiro ; Telszewski, Maciej ; Nojiri, Yukihiro ; Mikaloff Fletcher, Sara E. ; Niwa, Y. ; Patra, Prabir K. ; Valsala, V. ; Nakano, Hideyuki ; Lima, Ivan D. ; Doney, Scott C. ; Buitenhuis, Erik T. ; Aumont, Olivier ; Dunne, John P. ; Lenton, Andrew ; Takahashi, Taro

Air–sea CO2 fluxes over the Pacific Ocean are known to be characterized by coherent large-scale structures that reflect not only ocean subduction and upwelling patterns, but also the combined effects of wind-driven gas exchange and biology. On the largest scales, a large net CO2 influx into the extratropics is associated with a robust seasonal cycle, and a large net CO2 efflux from the tropics is associated with substantial interannual variability. In this work, we have synthesized estimates of the net air–sea CO2 flux from a variety of products, drawing upon a variety of approaches in three sub-basins of the Pacific Ocean, i.e., the North Pacific extratropics (18–66° N), the tropical Pacific (18° S–18° N), and the South Pacific extratropics (44.5–18° S). These approaches include those based on the measurements of CO2 partial pressure in surface seawater (pCO2sw), inversions of ocean-interior CO2 data, forward ocean biogeochemistry models embedded in the ocean general circulation models (OBGCMs), a model with assimilation of pCO2sw data, and inversions of atmospheric CO2 measurements. Long-term means, interannual variations and mean seasonal variations of the regionally integrated fluxes were compared in each of the sub-basins over the last two decades, spanning the period from 1990 through 2009. A simple average of the long-term mean fluxes obtained with surface water pCO2 diagnostics and those obtained with ocean-interior CO2 inversions are −0.47 ± 0.13 Pg C yr−1 in the North Pacific extratropics, +0.44 ± 0.14 Pg C yr−1 in the tropical Pacific, and −0.37 ± 0.08 Pg C yr−1 in the South Pacific extratropics, where positive fluxes are into the atmosphere. This suggests that approximately half of the CO2 taken up over the North and South Pacific extratropics is released back to the atmosphere from the tropical Pacific. These estimates of the regional fluxes are also supported by the estimates from OBGCMs after adding the riverine CO2 flux, i.e., −0.49 ± 0.02 Pg C yr−1 in the North Pacific extratropics, +0.41 ± 0.05 Pg C yr−1 in the tropical Pacific, and −0.39 ± 0.11 Pg C yr−1 in the South Pacific extratropics. The estimates from the atmospheric CO2 inversions show large variations amongst different inversion systems, but their median fluxes are consistent with the estimates from climatological pCO2sw data and pCO2sw diagnostics. In the South Pacific extratropics, where CO2 variations in the surface and ocean interior are severely undersampled, the difference in the air–sea CO2 flux estimates between the diagnostic models and ocean-interior CO2 inversions is larger (0.18 Pg C yr−1). The range of estimates from forward OBGCMs is also large (−0.19 to −0.72 Pg C yr−1). Regarding interannual variability of air–sea CO2 fluxes, positive and negative anomalies are evident in the tropical Pacific during the cold and warm events of the El Niño–Southern Oscillation in the estimates from pCO2sw diagnostic models and from OBGCMs. They are consistent in phase with the Southern Oscillation Index, but the peak-to-peak amplitudes tend to be higher in OBGCMs (0.40 ± 0.09 Pg C yr−1) than in the diagnostic models (0.27 ± 0.07 Pg C yr−1).
Changes in deep-water CO2 concentrations over the last several decades determined from discrete pCO2 measurements

(Elsevier Ltd, 2013-02-09) Wanninkhof, Rik ; Park, Geun-Ha ; Takahashi, Taro ; Feely, Richard A. ; Bullister, John L. ; Doney, Scott C.

Detection and attribution of hydrographic and biogeochemical changes in the deep ocean are challenging due to the small magnitude of their signals and to limitations in the accuracy of available data. However, there are indications that anthropogenic and climate change signals are starting to manifest at depth. The deep ocean below 2000 m comprises about 50% of the total ocean volume, and changes in the deep ocean should be followed over time to accurately assess the partitioning of anthropogenic carbon dioxide (CO2) between the ocean, terrestrial biosphere, and atmosphere. Here we determine the changes in the interior deep-water inorganic carbon content by a novel means that uses the partial pressure of CO2 measured at 20 °C, pCO2(20), along three meridional transects in the Atlantic and Pacific oceans. These changes are measured on decadal time scales using observations from the World Ocean Circulation Experiment (WOCE)/World Hydrographic Program (WHP) of the 1980s and 1990s and the CLIVAR/CO2 Repeat Hydrography Program of the past decade. The pCO2(20) values show a consistent increase in deep water over the time period. Changes in total dissolved inorganic carbon (DIC) content in the deep interior are not significant or consistent, as most of the signal is below the level of analytical uncertainty. Using an approximate relationship between pCO2(20) and DIC change, we infer DIC changes that are at the margin of detectability. However, when integrated on the basin scale, the increases range from 8–40% of the total specific water column changes over the past several decades. Patterns in chlorofluorocarbons (CFCs), along with output from an ocean model, suggest that the changes in pCO2(20) and DIC are of anthropogenic origin.
Anthropogenic 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, Andrew

The 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.
Spatiotemporal variability and long-term trends of ocean acidification in the California Current System

(Copernicus Publications on behalf of the European Geosciences Union, 2013-01-14) Hauri, Claudine ; Gruber, Nicolas ; Vogt, Meike ; Doney, Scott C. ; Feely, Richard A. ; Lachkar, Z. ; Leinweber, A. ; McDonnell, Andrew M. P. ; Munnich, M. ; Plattner, Gian-Kasper

Due to seasonal upwelling, the upper ocean waters of the California Current System (CCS) have a naturally low pH and aragonite saturation state (Ωarag), making this region particularly prone to the effects of ocean acidification. Here, we use the Regional Oceanic Modeling System (ROMS) to conduct preindustrial and transient (1995–2050) simulations of ocean biogeochemistry in the CCS. The transient simulations were forced with increasing atmospheric pCO2 and increasing oceanic dissolved inorganic carbon concentrations at the lateral boundaries, as projected by the NCAR CSM 1.4 model for the IPCC SRES A2 scenario. Our results show a large seasonal variability in pH (range of ~ 0.14) and Ωarag (~ 0.2) for the nearshore areas (50 km from shore). This variability is created by the interplay of physical and biogeochemical processes. Despite this large variability, we find that present-day pH and Ωarag have already moved outside of their simulated preindustrial variability envelopes (defined by ±1 temporal standard deviation) due to the rapidly increasing concentrations of atmospheric CO2. The nearshore surface pH of the northern and central CCS are simulated to move outside of their present-day variability envelopes by the mid-2040s and late 2030s, respectively. This transition may occur even earlier for nearshore surface Ωarag, which is projected to depart from its present-day variability envelope by the early- to mid-2030s. The aragonite saturation horizon of the central CCS is projected to shoal into the upper 75 m within the next 25 yr, causing near-permanent undersaturation in subsurface waters. Due to the model's overestimation of Ωarag, this transition may occur even earlier than simulated by the model. Overall, our study shows that the CCS joins the Arctic and Southern oceans as one of only a few known ocean regions presently approaching the dual threshold of widespread and near-permanent undersaturation with respect to aragonite and a departure from its variability envelope. In these regions, organisms may be forced to rapidly adjust to conditions that are both inherently chemically challenging and also substantially different from past conditions.
Ocean acidification risk assessment for Alaska’s fishery sector

(Elsevier, 2014-07-14) Mathis, Jeremy T. ; Cooley, Sarah R. ; Lucey, Noelle ; Colt, Steve ; Ekstrom, Julia ; Hurst, Tom ; Hauri, Claudine ; Evans, Wiley ; Cross, Jessica N. ; Feely, Richard A.

The highly productive fisheries of Alaska are located in seas projected to experience strong global change, including rapid transitions in temperature and ocean acidification-driven changes in pH and other chemical parameters. Many of the marine organisms that are most intensely affected by ocean acidification (OA) contribute substantially to the state’s commercial fisheries and traditional subsistence way of life. Prior studies of OA’s potential impacts on human communities have focused only on possible direct economic losses from specific scenarios of human dependence on commercial harvests and damages to marine species. However, other economic and social impacts, such as changes in food security or livelihoods, are also likely to result from climate change. This study evaluates patterns of dependence on marine resources within Alaska that could be negatively impacted by OA and current community characteristics to assess the potential risk to the fishery sector from OA. Here, we used a risk assessment framework based on one developed by the Intergovernmental Panel on Climate Change to analyze earth-system global ocean model hindcasts and projections of ocean chemistry, fisheries harvest data, and demographic information. The fisheries examined were: shellfish, salmon and other finfish. The final index incorporates all of these data to compare overall risk among Alaska’s federally designated census areas. The analysis showed that regions in southeast and southwest Alaska that are highly reliant on fishery harvests and have relatively lower incomes and employment alternatives likely face the highest risk from OA. Although this study is an intermediate step toward our full understanding, the results presented here show that OA merits consideration in policy planning, as it may represent another challenge to Alaskan communities, some of which are already under acute socio-economic strains.
Ocean acidification : a critical emerging problem for the ocean sciences

(Oceanography Society, 2009-12) Doney, Scott C. ; Balch, William M. ; Fabry, Victoria J. ; Feely, Richard A.

Over a period of less than a decade, ocean acidification—the change in seawater chemistry due to rising atmospheric carbon dioxide (CO2) levels and subsequent impacts on marine life—has become one of the most critical and pressing issues facing the ocean research community and marine resource managers alike. The objective of this special issue of Oceanography is to provide an overview of the current scientific understanding of ocean acidification as well as to indicate the substantial gaps in our present knowledge. Papers in the special issue discuss the past, current, and future trends in seawater chemistry; highlight potential vulnerabilities to marine species, ecosystems, and marine resources to elevated CO2; and outline a roadmap toward future research directions. In this introductory article, we present a brief introduction on ocean acidification and some historical context for how it emerged so quickly and recently as a key research topic.
Ocean acidification : present conditions and future changes in a high-CO2 world

(Oceanography Society, 2009-12) Feely, Richard A. ; Doney, Scott C. ; Cooley, Sarah R.

The uptake of anthropogenic CO2 by the global ocean induces fundamental changes in seawater chemistry that could have dramatic impacts on biological ecosystems in the upper ocean. Estimates based on the Intergovernmental Panel on Climate Change (IPCC) business-as-usual emission scenarios suggest that atmospheric CO2 levels could approach 800 ppm near the end of the century. Corresponding biogeochemical models for the ocean indicate that surface water pH will drop from a pre-industrial value of about 8.2 to about 7.8 in the IPCC A2 scenario by the end of this century, increasing the ocean’s acidity by about 150% relative to the beginning of the industrial era. In contemporary ocean water, elevated CO2 will also cause substantial reductions in surface water carbonate ion concentrations, in terms of either absolute changes or fractional changes relative to pre-industrial levels. For most open-ocean surface waters, aragonite undersaturation occurs when carbonate ion concentrations drop below approximately 66 μmol kg-1. The model projections indicate that aragonite undersaturation will start to occur by about 2020 in the Arctic Ocean and 2050 in the Southern Ocean. By 2050, all of the Arctic will be undersaturated with respect to aragonite, and by 2095, all of the Southern Ocean and parts of the North Pacific will be undersaturated. For calcite, undersaturation occurs when carbonate ion concentration drops below 42 μmol kg-1. By 2095, most of the Arctic and some parts of the Bering and Chukchi seas will be undersaturated with respect to calcite. However, in most of the other ocean basins, the surface waters will still be saturated with respect to calcite, but at a level greatly reduced from the present.
Changes in ocean heat, carbon content, and ventilation : a review of the first decade of GO-SHIP Global Repeat Hydrography

( 2015-05-30) Talley, Lynne D. ; Feely, Richard A. ; Sloyan, Bernadette M. ; Wanninkhof, Rik ; Baringer, Molly O. ; Bullister, John L. ; Carlson, Craig A. ; Doney, Scott C. ; Fine, Rana A. ; Firing, Eric ; Gruber, Nicolas ; Hansell, Dennis A. ; Ishii, Masayoshi ; Johnson, Gregory ; Katsumata, K. ; Key, Robert M. ; Kramp, Martin ; Langdon, Chris ; Macdonald, Alison M. ; Mathis, Jeremy T. ; McDonagh, Elaine L. ; Mecking, Sabine ; Millero, Frank J. ; Mordy, Calvin W. ; Nakano, T. ; Sabine, Chris L. ; Smethie, William M. ; Swift, James H. ; Tanhua, Toste ; Thurnherr, Andreas M. ; Warner, Mark J. ; Zhang, Jia-Zhong

The ocean, a central component of Earth’s climate system, is changing. Given the global scope of these changes, highly accurate measurements of physical and biogeochemical properties need to be conducted over the full water column, spanning the ocean basins from coast to coast, and repeated every decade at a minimum, with a ship-based observing system. Since the late 1970s, when the Geochemical Ocean Sections Study (GEOSECS) conducted the first global survey of this kind, the World Ocean Circulation Experiment (WOCE) and Joint Global Ocean Flux Study (JGOFS), and now the Global Ocean Ship-based Hydrographic Investigations Program (GO-SHIP) have collected these “reference standard” data that allow quantification of ocean heat and carbon uptake, and variations in salinity, oxygen, nutrients, and acidity on basin scales. The evolving GO-SHIP measurement suite also provides new global information about dissolved organic carbon, a large bioactive reservoir of carbon.
Variability and trends in surface seawater pCO2 and CO2 flux in the Pacific Ocean

(John Wiley & Sons, 2017-06-12) Sutton, Adrienne J. ; Wanninkhof, Rik ; Sabine, Christopher L. ; Feely, Richard A. ; Cronin, Meghan F. ; Weller, Robert A.

Variability and change in the ocean sink of anthropogenic carbon dioxide (CO2) have implications for future climate and ocean acidification. Measurements of surface seawater CO2 partial pressure (pCO2) and wind speed from moored platforms are used to calculate high-resolution CO2 flux time series. Here we use the moored CO2 fluxes to examine variability and its drivers over a range of time scales at four locations in the Pacific Ocean. There are significant surface seawater pCO2, salinity, and wind speed trends in the North Pacific subtropical gyre, especially during winter and spring, which reduce CO2 uptake over the 10 year record of this study. Starting in late 2013, elevated seawater pCO2 values driven by warm anomalies cause this region to be a net annual CO2 source for the first time in the observational record, demonstrating how climate forcing can influence the timing of an ocean region shift from CO2 sink to source.
Best practice data standards for discrete chemical oceanographic observations

(Frontiers Media, 2022-01-21) Jiang, Li-Qing ; Pierrot, Denis ; Wanninkhof, Rik ; Feely, Richard A. ; Tilbrook, Bronte ; Alin, Simone R. ; Barbero, Leticia ; Byrne, Robert H. ; Carter, Brendan ; Dickson, Andrew G. ; Gattuso, Jean-Pierre ; Greeley, Dana ; Hoppema, Mario ; Humphreys, Matthew P. ; Karstensen, Johannes ; Lange, Nico ; Lauvset, Siv K. ; Lewis, Ernie R. ; Olsen, Are ; Perez, Fiz F. ; Sabine, Christopher ; Sharp, Jonathan D. ; Tanhua, Toste ; Trull, Thomas W. ; Velo, Anton ; Allegra, Andrew J. ; Barker, Paul M. ; Burger, Eugene ; Cai, Wei-Jun ; Chen, Chen-Tung A. ; Cross, Jessica N. ; Garcia, Hernan E. ; Hernandez-Ayon, Jose Martin ; Hu, Xinping ; Kozyr, Alex ; Langdon, Chris ; Lee, Kitack ; Salisbury, Joseph E. ; Wang, Zhaohui Aleck ; Xue, Liang

Effective data management plays a key role in oceanographic research as cruise-based data, collected from different laboratories and expeditions, are commonly compiled to investigate regional to global oceanographic processes. Here we describe new and updated best practice data standards for discrete chemical oceanographic observations, specifically those dealing with column header abbreviations, quality control flags, missing value indicators, and standardized calculation of certain properties. These data standards have been developed with the goals of improving the current practices of the scientific community and promoting their international usage. These guidelines are intended to standardize data files for data sharing and submission into permanent archives. They will facilitate future quality control and synthesis efforts and lead to better data interpretation. In turn, this will promote research in ocean biogeochemistry, such as studies of carbon cycling and ocean acidification, on regional to global scales. These best practice standards are not mandatory. Agencies, institutes, universities, or research vessels can continue using different data standards if it is important for them to maintain historical consistency. However, it is hoped that they will be adopted as widely as possible to facilitate consistency and to achieve the goals stated above.
Pacific anthropogenic carbon between 1991 and 2017

(American Geophysical Union, 2019-04-29) Carter, Brendan ; Feely, Richard A. ; Wanninkhof, Rik ; Kouketsu, Shinya ; Sonnerup, Rolf E. ; Pardo, Paula Conde ; Sabine, Christopher L. ; Johnson, Gregory C. ; Sloyan, Bernadette M. ; Murata, Akihiko ; Mecking, Sabine ; Tilbrook, Bronte ; Speer, Kevin G. ; Talley, Lynne D. ; Millero, Frank J. ; Wijffels, Susan E. ; Macdonald, Alison M. ; Gruber, Nicolas ; Bullister, John L.

We estimate anthropogenic carbon (Canth) accumulation rates in the Pacific Ocean between 1991 and 2017 from 14 hydrographic sections that have been occupied two to four times over the past few decades, with most sections having been recently measured as part of the Global Ocean Ship‐based Hydrographic Investigations Program. The rate of change of Canth is estimated using a new method that combines the extended multiple linear regression method with improvements to address the challenges of analyzing multiple occupations of sections spaced irregularly in time. The Canth accumulation rate over the top 1,500 m of the Pacific increased from 8.8 (±1.1, 1σ) Pg of carbon per decade between 1995 and 2005 to 11.7 (±1.1) PgC per decade between 2005 and 2015. For the entire Pacific, about half of this decadal increase in the accumulation rate is attributable to the increase in atmospheric CO2, while in the South Pacific subtropical gyre this fraction is closer to one fifth. This suggests a substantial enhancement of the accumulation of Canth in the South Pacific by circulation variability and implies that a meaningful portion of the reinvigoration of the global CO2 sink that occurred between ~2000 and ~2010 could be driven by enhanced ocean Canth uptake and advection into this gyre. Our assessment suggests that the accuracy of Canth accumulation rate reconstructions along survey lines is limited by the accuracy of the full suite of hydrographic data and that a continuation of repeated surveys is a critical component of future carbon cycle monitoring.
Storm-induced upwelling of high pCO2 waters onto the continental shelf of the western Arctic Ocean and implications for carbonate mineral saturation states

(American Geophysical Union, 2012-04-11) Mathis, Jeremy T. ; Pickart, Robert S. ; Byrne, Robert H. ; McNeil, Craig L. ; Moore, G. W. K. ; Juranek, Laurie W. ; Liu, Xuewu ; Ma, Jian ; Easley, Regina A. ; Elliot, Matthew M. ; Cross, Jessica N. ; Reisdorph, Stacey C. ; Bahr, Frank B. ; Morison, James H. ; Lichendorf, Trina ; Feely, Richard A.

The carbon system of the western Arctic Ocean is undergoing a rapid transition as sea ice extent and thickness decline. These processes are dynamically forcing the region, with unknown consequences for CO2 fluxes and carbonate mineral saturation states, particularly in the coastal regions where sensitive ecosystems are already under threat from multiple stressors. In October 2011, persistent wind-driven upwelling occurred in open water along the continental shelf of the Beaufort Sea in the western Arctic Ocean. During this time, cold (<−1.2°C), salty (>32.4) halocline water—supersaturated with respect to atmospheric CO2 (pCO2 > 550 μatm) and undersaturated in aragonite (Ωaragonite < 1.0) was transported onto the Beaufort shelf. A single 10-day event led to the outgassing of 0.18–0.54 Tg-C and caused aragonite undersaturations throughout the water column over the shelf. If we assume a conservative estimate of four such upwelling events each year, then the annual flux to the atmosphere would be 0.72–2.16 Tg-C, which is approximately the total annual sink of CO2 in the Beaufort Sea from primary production. Although a natural process, these upwelling events have likely been exacerbated in recent years by declining sea ice cover and changing atmospheric conditions in the region, and could have significant impacts on regional carbon budgets. As sea ice retreat continues and storms increase in frequency and intensity, further outgassing events and the expansion of waters that are undersaturated in carbonate minerals over the shelf are probable.

Feely Richard A.

Last Name

First Name

ORCID

Filters

Author

Subject

Date

Type

Has files

Settings

Sort By

Results per page

Search Results