13.0: A Changing Ocean
Anthropogenic perturbations to the global Earth system have included important alterations in the chemical composition, temperature, and circulation of the oceans. Some of these changes will be distinguishable from the background natural variability in nearly half of the global open ocean within a decade, with important consequences for marine ecosystems and their services.1 However, the timeframe for detection will vary depending on the parameter featured.2 ,3
13.1: Ocean Warming
13.1.1 General Background
Approximately 93% of excess heat energy trapped since the 1970s has been absorbed into the oceans, lessening atmospheric warming and leading to a variety of changes in ocean conditions, including sea level rise and ocean circulation (see Ch. 2: Physical Drivers of Climate Change, Ch. 6: Temperature Change, and Ch. 12: Sea Level Rise in this report).1 ,4 This is the result of the high heat capacity of seawater relative to the atmosphere, the relative area of the ocean compared to the land, and the ocean circulation that enables the transport of heat into deep waters. This large heat absorption by the oceans moderates the effects of increased anthropogenic greenhouse emissions on terrestrial climates while altering the fundamental physical properties of the ocean and indirectly impacting chemical properties such as the biological pump through increased stratification.1 ,5 Although upper ocean temperature varies over short- and medium timescales (for example, seasonal and regional patterns), there are clear long-term increases in surface temperature and ocean heat content over the past 65 years.4 ,6 ,7
13.1.2 Ocean Heat Content
Ocean heat content (OHC) is an ideal variable to monitor changing climate as it is calculated using the entire water column, so ocean warming can be documented and compared between particular regions, ocean basins, and depths. However, for years prior to the 1970s, estimates of ocean uptake are confined to the upper ocean (up to 700 m) due to sparse spatial and temporal coverage and limited vertical capabilities of many of the instruments in use. OHC estimates are improved for time periods after 1970 with increased sampling coverage and depth.4 ,8 Estimates of OHC have been calculated going back to the 1950s using averages over longer time intervals (i.e., decadal or 5-year intervals) to compensate for sparse data distributions, allowing for clear long-term trends to emerge (e.g., Levitus et al. 20127 ).
From 1960 to 2015, OHC significantly increased for both 0–700 and 700–2,000 m depths, for a total ocean warming of about 33.5 ± 7.0 × 1022 J (a net heating of 0.37 ± 0.08 W/m2; Figure 13.1).6 During this period, there is evidence of an acceleration of ocean warming beginning in 1998,9 with a total heat increase of about 15.2 × 1022 J.6 Robust ocean warming occurs in the upper 700 m and is slow to penetrate into the deep ocean. However, the 700–2,000 m depths constitute an increasing portion of the total ocean energy budget as compared to the surface ocean (Figure 13.1).6 The role of the deep ocean (below 2,000 m [6,600 ft]) in ocean heat uptake remains uncertain, both in the magnitude but also the sign of the uptake.10 ,11 Penetration of surface waters to the deep ocean is a slow process, which means that while it takes only about a decade for near-surface temperatures to respond to increased heat energy, the deep ocean will continue to warm, and as a result sea levels will rise for centuries to millennia even if all further emissions cease.4
Several sources have documented warming in all ocean basins from 0–2,000 m depths over the past 50 years (Figure 13.2).6 ,7 ,12 Annual fluctuations in surface temperatures and OHC are attributed to the combination of a long-term secular trend and decadal and smaller time scale variations, such as the Pacific Decadal Oscillation (PDO) and the Atlantic Multidecadal Oscillation (AMO) (Ch. 5: Circulation & Variability; Ch. 12: Sea Level Rise).13 ,14 The transport of heat to the deep ocean is likely linked to the strength of the Atlantic Meridional Overturning Circulation (see Section 13.2.1), where the Atlantic and Southern Ocean accounts for the dominant portion of total OHC change at the 700–2,000 m depth.6 ,8 ,9 ,15 Decadal variability in ocean heat uptake is mostly attributed to ENSO phases (with El Niños warming and La Niñas cooling). For instance, La Niña conditions over the past decade have led to colder ocean temperatures in the eastern tropical Pacific.6 ,8 ,9 ,16 For the Pacific and Indian Oceans, the decadal shifts are primarily observed in the upper 350 m depth, likely due to shallow subtropical circulation, leading to an abrupt increase of OHC in the Indian Ocean carried by the Indonesian throughflow from the Pacific Ocean over the last decade.9 Although there is natural variability in ocean temperature, there remain clear increasing trends due to anthropogenic influences.
13.1.3 Sea Surface Temperature and U.S. Regional Warming
In addition to OHC, sea surface temperature (SST) measurements are widely available. SST measurements are useful because 1) the measurements have been taken over 150 years (albeit using different platforms, instruments, and depths through time); 2) SST reflects the lower boundary condition of the atmosphere; and 3) SST can be used to predict specific regional impacts of global warming on terrestrial and coastal systems.15 ,17 ,18 Globally, surface ocean temperatures have increased by 1.3° ± 0.1°F (0.70° ± 0.08°C) per century from 1900 to 2016 for the Extended Reconstructed Sea Surface Temperature version 4 (ERSST v4) record.19 All U.S. coastal waters have warmed by more than 0.7°F (0.4°C) over this period as shown in both Table 13.1 and Chapter 6: Temperature Change, Figure 6.6. During the past 60 years, the rates of increase of SSTs for the coastal waters of three U.S. regions were above the global average rate. These included the waters around Alaska, the Northeast, and the Southwest (Table 13.1). Over the last decade, some regions have experienced increased high ocean temperature anomalies. SST in the Northeast has warmed faster than 99% of the global ocean since 2004, and a peak temperature for the region in 2012 was part of a large “ocean heat wave” in the Northwest Atlantic that persisted for nearly 18 months.20 ,21 Projections indicate that the Northeast will continue to warm more quickly than other ocean regions through the end of the century.22 In the Northwest, a resilient ridge of high pressure over the North American West Coast suppressed storm activity and mixing, which intensified heat in the upper ocean in a phenomenon known as “The Blob”.23 Anomalously warm waters persisted in the coastal waters of the Alaskan and Pacific Northwest from 2013 until 2015. Under a higher scenario (RCP8.5), SSTs are projected to increase by an additional 4.9°F (2.7°C) by 2100 (Figure 13.3), whereas for a lower scenario (RCP4.5) the SST increase would be 2.3°F (1.3°C).24 In all U.S. coastal regions, the warming since 1901 is detectable compared to natural variability and attributable to anthropogenic forcing, according to an analysis of the CMIP5 models (Ch. 6: Temperature Change, Figure 6.5).
Region | latitude and longitude |
Historical Trend (°C/100 years) |
Projected Trend 2080 (relative to 1976‐2005 climate) (°C) |
||
---|---|---|---|---|---|
1900–2016 | 1950–2016 | RCP4.5 | RCP8.5 | ||
Global | 0.70 – 0.08 | 1.00 – 0.11 | 1.3 – 0.6 | 2.7 – 0.7 | |
Alaska |
50°–66°N 150°–170°W |
0.82 – 0.26 | 1.22 – 0.59 | 2.5 – 0.6 | 3.7 – 1.0 |
Northwest (NW) |
40°–50°N 120°–132°W |
0.64 – 0.30 | 0.68 – 0.70 | 1.7 – 0.4 | 2.8 – 0.6 |
Southwest (SW) |
30°–40°N 116°–126°W |
0.73 – 0.33 | 1.02 – 0.79 | ||
Hawaii (HI) |
18°–24°N 152°–162°W |
0.58 – 0.19 | 0.46 – 0.39 | 1.6 – 0.4 | 2.8 – 0.6 |
Northeast (NE) |
36°–46°N 64°–76°W |
0.63 – 0.31 | 1.10 – 0.71 | 2.0 – 0.3 | 3.2 – 0.6 |
Southeast (SE) |
24°–34°N 64°–80°W |
0.40 – 0.18 | 0.13 – 0.34 | 1.6 – 0.3 | 2.7 – 0.4 |
Gulf of Mexico (GOM) |
20°–30°N 80°–96°W |
0.52 – 0.14 | 0.37 – 0.27 | 1.6 – 0.3 | 2.8 – 0.3 |
Caribbean |
10°–20°N 66°–86°W |
0.76 – 0.15 | 0.77 – 0.32 | 1.5 – 0.4 | 2.6 – 0.3 |
Figure 13.3
13.1.4 Ocean Heat Feedback
The residual heat not taken up by the oceans increases land surface temperatures (approximately 3%) and atmospheric temperatures (approximately 1%), and melts both land and sea ice (approximately 3%), leading to sea level rise (see Ch. 12: Sea Level Rise).4 ,6 ,25 The meltwater from land and sea ice amplifies further subsurface ocean warming and ice shelf melting, primarily due to increased thermal stratification, which reduces the ocean’s efficiency in transporting heat to deep waters.4 Surface ocean stratification has increased by about 4% during the period 1971–201026 due to thermal heating and freshening from increased freshwater inputs (precipitation and evaporation changes and land and sea ice melting). The increase of ocean stratification will contribute to further feedback of ocean warming and, indirectly, mean sea level. In addition, increases in stratification are associated with suppression of tropical cyclone intensification,27 retreat of the polar ice sheets,28 and reductions of the convective mixing at higher latitudes that transports heat to the deep ocean through the Atlantic Meridional Overturning Circulation.29 Ocean heat uptake therefore represents an important feedback that will have a significant influence on future shifts in climate (see Ch. 2: Physical Drivers of Climate Change).
13.2: Ocean Circulation
13.2.1 Atlantic Meridional Overturning Circulation
The Atlantic Meridional Overturning Circulation (AMOC) refers to the three-dimensional, time-dependent circulation of the Atlantic Ocean, which has been a high priority topic of study in recent decades. The AMOC plays an important role in climate through its transport of heat, freshwater, and carbon (e.g., Johns et al. 2011;30 McDonagh et al. 2015;31 Talley et al. 201632 ). AMOC-associated poleward heat transport substantially contributes to North American and continental European climate (see Ch. 5: Circulation and Variability). The Gulf Stream, in contrast to other western boundary currents, is expected to slow down because of the weakening of the AMOC, which would impact the European climate.33 Variability in the AMOC has been attributed to wind forcing on intra-annual time scales and to geostrophic forces on interannual to decadal timescales.34 Increased freshwater fluxes from melting Arctic Sea and land ice can weaken open ocean convection and deep-water formation in the Labrador and Irminger Seas, which could weaken the AMOC (Ch. 11: Arctic Changes; also see Ch. 5, Section 5.2.3: North Atlantic Oscillation and Northern Annular Mode).29 ,33
While one recent study has suggested that the AMOC has slowed since preindustrial times29 and another suggested slowing on faster time scales,35 there is at present insufficient observational evidence to support a finding of long term slowdown of AMOC strength over the 20th century4 or within the last 50 years34 as decadal ocean variability can obscure long-term trends. Some studies show long-term trends,36 ,37 but the combination of sparse data and large seasonal variability may also lead to incorrect interpretations (e.g., Kanzow et al. 201038 ). Several recent high resolution modeling studies constrained with the limited existing observational data39 and/or with reconstructed freshwater fluxes40 suggest that the recently observed AMOC slowdown at 26°N (off the Florida coast) since 2004 (e.g., as described in Smeed et al. 201435 ) is mainly due to natural variability, and that anthropogenic forcing has not yet caused a significant AMOC slowdown. In addition, direct observations of the AMOC in the South Atlantic fail to unambiguously demonstrate anthropogenic trends (e.g., Dong et al. 2015;41 Garzoli et al. 201342 ).
Under a higher scenario (RCP8.5) in CMIP5 simulations, it is very likely that the AMOC will weaken over the 21st century. The projected decline ranges from 12% to 54%,43 with the range width reflecting substantial uncertainty in quantitative projections of AMOC behavior. In lower scenarios (like RCP4.5), CMIP5 models predict a 20% weakening of the AMOC during the first half of the 21st century and a stabilization and slight recovery after that.44 The projected slowdown of the AMOC will be counteracted by the warming of the deep ocean (below 700 m [2,300 ft]), which will tend to strengthen the AMOC.45 The situation is further complicated due to the known bias in coupled climate models related to the direction of the salinity transport in models versus observations, which is an indicator of AMOC stability (e.g., Drijhout et al. 2011;46 Bryden et al. 2011;47 Garzoli et al. 201342 ). Some argue that coupled climate models should be corrected for this known bias and that AMOC variations could be even larger than the gradual decrease most models predict if the AMOC were to shut down completely and “flip states”.48 Any AMOC slowdown could result in less heat and CO2 absorbed by the ocean from the atmosphere, which is a positive feedback to climate change (also see Ch. 2: Physical Drivers of Climate Change).49 ,50 ,51
13.2.2 Changes in Salinity Structure
As a response to warming, increased atmospheric moisture leads to stronger evaporation or precipitation in terrestrial and oceanic environments and melting of land and sea ice. Approximately 80% of precipitation/evaporation events occur over the ocean, leading to patterns of higher salt content or freshwater anomalies and changes in ocean circulation (see Ch. 2: Physical Drivers of Climate Change and Ch. 6: Temperature Change).52 Over 1950–2010, average global amplification of the surface salinity pattern amounted to 5.3%; where fresh regions in the ocean became fresher and salty regions became saltier.53 However, the long-term trends of these physical and chemical changes to the ocean are difficult to isolate from natural large-scale variability. In particular, ENSO displays particular salinity and precipitation/evaporation patterns that skew the trends. More research and data are necessary to better model changes to ocean salinity. Several models have shown a similar spatial structure of surface salinity changes, including general salinity increases in the subtropical gyres, a strong basin-wide salinity increase in the Atlantic Ocean, and reduced salinity in the western Pacific warm pools and the North Pacific subpolar regions.52 ,53 There is also a stronger distinction between the upper salty thermocline and fresh intermediate depth through the century. The regional changes in salinity to ocean basins will have an overall impact on ocean circulation and net primary production, leading to corresponding carbon export (see Ch. 2: Physical Drivers of Climate Change). In particular, the freshening of the Arctic Ocean due to melting of land and sea ice can lead to buoyancy changes which could slow down the AMOC (see Section 13.2.1).
13.2.3 Changes in Upwelling
Significant changes to ocean stratification and circulation can also be observed regionally, along the eastern ocean boundaries and at the equator. In these areas, wind-driven upwelling brings colder, nutrient- and carbon-rich water to the surface; this upwelled water is more efficient in heat and anthropogenic CO2 uptake. There is some evidence that coastal upwelling in mid- to high-latitude eastern boundary regions has increased in intensity and/or frequency,54 but in more tropical areas of the western Atlantic, such as in the Caribbean Sea, it has decreased between 1990 and 2010.55 ,56 This has led to a decrease in primary productivity in the southern Caribbean Sea.55 Within the continental United States, the California Current is experiencing fewer (by about 23%–40%) but stronger upwelling events.57 ,58 ,59 Stronger offshore upwelling combined with cross-shelf advection brings nutrients from the deeper ocean but also increased offshore transport.60 The net nutrient load in the coastal regions is responsible for increased productivity and ecosystem function.
IPCC 2013 concluded that there is low confidence in the current understanding of how eastern upwelling systems will be altered under future climate change because of the obscuring role of multidecadal climate variability.26 However, subsequent studies show that by 2100, upwelling is predicted to start earlier in the year, end later, and intensify in three of the four major eastern boundary upwelling systems (not in the California Current).61 In the California Current, upwelling is projected to intensify in spring but weaken in summer, with changes emerging from the envelope of natural variability primarily in the second half of the 21st century.62 Southern Ocean upwelling will intensify while the Atlantic equatorial upwelling systems will weaken.57 ,61 The intensification is attributed to the strengthening of regional coastal winds as observations already show,58 and model projections under the higher scenario (RCP8.5) estimate wind intensifying near poleward boundaries (including northern California Current) and weakening near equatorward boundaries (including southern California Current) for the 21st century.61 ,63
13.3: Ocean Acidification
13.3.1 General Background
In addition to causing changes in climate, increasing atmospheric levels of carbon dioxide (CO2) from the burning of fossil fuels and other human activities, including changes in land use, have a direct effect on ocean carbonate chemistry that is termed ocean acidification.64 ,65 Surface ocean waters absorb part of the increasing CO2 in the atmosphere, which causes a variety of chemical changes in seawater: an increase in the partial pressure of CO2 (pCO2,sw), dissolved inorganic carbon (DIC), and the concentration of hydrogen and bicarbonate ions and a decrease in the concentration of carbonate ions (Figure 13.4). In brief, CO2 is an acid gas that combines with water to form carbonic acid, which then dissociates to hydrogen and bicarbonate ions. Increasing concentrations of seawater hydrogen ions result in a decrease of carbonate ions through their conversion to bicarbonate ions. The concentration of carbonate ions in seawater affects saturation states for calcium carbonate compounds, which many marine species use to build their shells and skeletons. Ocean acidity refers to the concentration of hydrogen ions in ocean seawater regardless of ocean pH, which is fundamentally basic (e.g., pH > 7). Ocean surface waters have become 30% more acidic over the last 150 years as they have absorbed large amounts of CO2 from the atmosphere,66 and anthropogenically sourced CO2 is gradually invading into oceanic deep waters. Since the preindustrial period, the oceans have absorbed approximately 29% of all CO2 emitted to the atmosphere.67 Oceans currently absorb about 26% of the human-caused CO2 anthropogenically emitted into the atmosphere.67
13.3.2 Open Ocean Acidification
Surface waters in the open ocean experience changes in carbonate chemistry reflective of large-scale physical oceanic processes (see Ch. 2: Physical Drivers of Climate Change). These processes include both the global uptake of atmospheric CO2 and the shoaling of naturally acidified subsurface waters due to vertical mixing and upwelling. In general, the rate of ocean acidification in open ocean surface waters at a decadal time-scale closely approximates the rate of atmospheric CO2 increase.68 Large, multidecadal phenomena such as the Atlantic Multidecadal Oscillation and Pacific Decadal Oscillation can add variability to the observed rate of change.68
13.3.3 Coastal Acidification
Coastal shelf and nearshore waters are influenced by the same processes as open ocean surface waters such as absorption of atmospheric CO2 and upwelling, as well as a number of additional, local-level processes, including freshwater, nutrient, sulfur, and nitrogen inputs.69 ,70 Coastal acidification generally exhibits higher-frequency variability and short-term episodic events relative to open-ocean acidification.71 ,72 ,73 ,74 Upwelling is of particular importance in coastal waters, especially along the U.S. West Coast. Deep waters that shoal with upwelling are enriched in CO2 due to uptake of anthropogenic atmospheric CO2 when last in contact with the atmosphere, coupled with deep water respiration processes and lack of gas exchange with the atmosphere.65 ,75 Freshwater inputs to coastal waters change seawater chemistry in ways that make it more susceptible to acidification, largely by freshening ocean waters and contributing varying amounts of dissolved inorganic carbon (DIC), total alkalinity (TA), dissolved and particulate organic carbon, and nutrients from riverine and estuarine sources. Coastal waters of the East Coast and mid-Atlantic are far more influenced by freshwater inputs than are Pacific Coast waters.76 Coastal waters can episodically experience riverine and glacial melt plumes that create conditions in which seawater can dissolve calcium carbonate structures.77 ,78 While these processes have persisted historically, climate-induced increases in glacial melt and high-intensity precipitation events can yield larger freshwater plumes than have occurred in the past. Nutrient runoff can increase coastal acidification by creating conditions that enhance biological respiration. In brief, nutrient loading typically promotes phytoplankton blooms, which, when they die, are consumed by bacteria. Bacteria respire CO2 and thus bacterial blooms can result in acidification events whose intensity depends on local hydrographic conditions, including water column stratification and residence time.72 Long-term changes in nutrient loading, precipitation, and/or ice melt may also impart long-term, secular changes in the magnitude of coastal acidification.
13.3.4 Latitudinal Variation
Ocean carbon chemistry is highly influenced by water temperature, largely because the solubility of CO2 in seawater increases as water temperature declines. Thus, cold, high-latitude surface waters can retain more CO2 than warm, lower-latitude surface waters.76 ,79 Because carbonate minerals also more readily dissolve in colder waters, these waters can more regularly become undersaturated with respect to calcium carbonate whereby mineral dissolution is energetically favored. This chemical state, often referred to as seawater being “corrosive” to calcium carbonate, is important when considering the ecological implications of ocean acidification as many species make structures such as shells and skeletons from calcium carbonate. Seawater conditions undersaturated with respect to calcium carbonate are common at depth, but currently and historically rare at the surface and near-surface.80 Some high-latitude surface and near-surface waters now experience such corrosive conditions, which are rarely documented in low-latitude surface or near-surface systems. For example, corrosive conditions at a range of ocean depths have been documented in the Arctic and northeastern Pacific Oceans.74 ,79 ,81 ,82 Storm-induced upwelling could cause undersaturation in tropical areas in the future.83 It is important to note that low-latitude waters are experiencing a greater absolute rate of change in calcium carbonate saturation state than higher latitudes, though these low-latitude waters are not approaching the undersaturated state except within near-shore or some benthic habitats.84
13.3.5 Paleo Evidence
Evidence suggests that the current rate of ocean acidification is the fastest in the last 66 million years (the K-Pg boundary) and possibly even the last 300 million years (when the first pelagic calcifiers evolved providing proxy information and also a strong carbonate buffer, characteristic of the modern ocean).85 ,86 The Paleo-Eocene Thermal Maximum (PETM; around 56 million years ago) is often referenced as the closest analogue to the present, although the overall rate of change in CO2 conditions during that event (estimated between 0.6 and 1.1 GtC/year) was much lower than the current increase in atmospheric CO2 of 10 GtC/year.86 ,87 The relatively slower rate of atmospheric CO2 increase at the PETM likely led to relatively small changes in carbonate ion concentration in seawater compared with the contemporary acidification rate, due to the ability of rock weathering to buffer the change over the longer time period.86 Some of the presumed acidification events in Earth’s history have been linked to selective extinction events suggestive of how guilds of species may respond to the current acidification event.85
13.3.6 Projected Changes
Projections indicate that by the end of the century under higher scenarios, such as SRES A1FI or RCP8.5, open-ocean surface pH will decline from the current average level of 8.1 to a possible average of 7.8 (Figure 13.5).1 When the entire ocean volume is considered under the same scenario, the volume of waters undersaturated with respect to calcium carbonate could expand from 76% in the 1990s to 91% in 2100, resulting in a shallowing of the saturation horizons—depths below which undersaturation occurs.1 ,88 Saturation horizons, which naturally vary among ocean basins, influence ocean carbon cycles and organisms with calcium carbonate structures, especially as they shoal into the zones where most biota lives.81 ,89 As discussed above, for a variety of reasons, not all ocean and coastal regions will experience acidification in the same way depending on other compounding factors. For instance, recent observational data from the Arctic Basin show that the Beaufort Sea became undersaturated, for part of the year, with respect to aragonite in 2001, while other continental shelf seas in the Arctic Basin are projected to do so closer to the middle of the century (e.g., the Chukchi Sea in about 2033 and Bering Sea in about 2062).90 Deviation from the global average rate of acidification will be especially true in coastal and estuarine areas where the rate of acidification is influenced by other drivers than atmospheric CO2, some of which are under the control of local management decisions (for example, nutrient pollution loads).
Figure 13.5
13.4: Ocean Deoxygenation
13.4.1 General Background
Oxygen is essential to most life in the ocean, governing a host of biogeochemical and biological processes. Oxygen influences metabolic, physiological, reproductive, behavioral, and ecological processes, ultimately shaping the composition, diversity, abundance, and distribution of organisms from microbes to whales. Increasingly, climate-induced oxygen loss (deoxygenation) associated with ocean warming and reduced ventilation to deep waters has become evident locally, regionally, and globally. Deoxygenation can also be attributed to anthropogenic nutrient input, especially in the coastal regions, where the nutrients can lead to the proliferation of primary production and, consequently, enhanced drawdown of dissolved oxygen by microbes.91 In addition, acidification (Section 13.2) can co-occur with deoxygenation as a result of warming-enhanced biological respiration.92 As aerobic organisms respire, O2 is consumed and CO2 is produced. Understanding the combined effect of both low O2 and low pH on marine ecosystems is an area of active research.93 Warming also raises biological metabolic rates which, in combination with intensified coastal and estuarine stratification, exacerbates eutrophication-induced hypoxia. We now see earlier onset and longer periods of seasonal hypoxia in many eutrophic sites, most of which occur in areas that are also warming.91
13.4.2 Climate Drivers of Ocean Deoxygenation
Global ocean deoxygenation is a direct effect of warming. Ocean warming reduces the solubility of oxygen (that is, warmer water can hold less oxygen) and changes physical mixing (for example, upwelling and circulation) of oxygen in the oceans. The increased temperature of global oceans accounts for about 15% of current global oxygen loss,94 although changes in temperature and oxygen are not uniform throughout the ocean.15 Warming also exerts direct influence on thermal stratification and enhances salinity stratification through ice melt and climate change-associated precipitation effects. Intensified stratification leads to reduced ventilation (mixing of oxygen into the ocean interior) and accounts for up to 85% of global ocean oxygen loss.94 Effects of ocean temperature change and stratification on oxygen loss are strongest in intermediate or mode waters at bathyal depths (in general, 200–3,000 m) and also nearshore and in the open ocean; these changes are especially evident in tropical and subtropical waters globally, in the Eastern Pacific,95 and in the Southern Ocean.94
There are also other, less direct effects of global temperature increase. Warming on land reduces terrestrial plant water efficiency (through effects on stomata; see Ch. 8: Drought, Floods, and Wildfires, Key Message 3), leading to greater runoff, on average, into coastal zones (see Ch. 8: Drought, Floods, and Wildfires for other hydrological effects of warming) and further enhancing hypoxia potential because greater runoff can mean more nutrient transport (See Ch. 2: Physical Drivers of Climate Change).96 ,97 Estuaries, especially ones with minimal tidal mixing, are particularly vulnerable to oxygen-depleted dead zones from the enhanced runoff and stratification. Warming can induce dissociation of frozen methane in gas hydrates buried on continental margins, leading to further drawdown of oxygen through aerobic methane oxidation in the water column.98 On eastern ocean boundaries, warming can enhance the land–sea temperature differential, causing increased upwelling due to higher winds with (a) greater nutrient input leading to production, sinking, decay, and biochemical drawdown of oxygen and (b) upwelling of naturally low-oxygen, high-CO2 waters onto the upper slope and shelf environments.58 ,65 However, in the California Current, upwelling intensification has occurred only in the poleward regions (north of San Francisco), and the drivers may not be associated with land–sea temperature differences.63 Taken together, the effects of warming are manifested as low-oxygen water in open oceans are being transported to and upwelled along coastal regions. These low-oxygen upwelled waters are then coupled with eutrophication-induced hypoxia, further reducing oxygen content in coastal areas.
Changes in precipitation, winds, circulation, airborne nutrients, and sea level can also contribute to ocean deoxygenation. Projected increases in precipitation in some regions will intensify stratification, reducing vertical mixing and ventilation, and intensify nutrient input to coastal waters through excess runoff, which leads to increased algal biomass and concurrent dissolved oxygen consumption via community respiration.99 Coastal wetlands that might remove these nutrients before they reach the ocean may be lost through rising sea level, further exacerbating hypoxia.97 Some observations of oxygen decline are linked to regional changes in circulation involving low-oxygen water masses. Enhanced fluxes of airborne iron and nitrogen are interacting with natural climate variability and contributing to fertilization, enhanced respiration, and oxygen loss in the tropical Pacific.100
13.4.3 Biogeochemical Feedbacks of Deoxygenation to Climate and Elemental Cycles
Climate patterns and ocean circulation have a large effect on global nitrogen and oxygen cycles, which in turn affect phosphorus and trace metal availability and generate feedbacks to the atmosphere and oceanic production. Global ocean productivity may be affected by climate-driven changes below the tropical and subtropical thermocline which control the volume of suboxic waters (< 5 micromolar O2), and consequently the loss of fixed nitrogen through denitrification.101 ,102 The extent of suboxia in the open ocean also regulates the production of the greenhouse gas nitrous oxide (N2O); as oxygen declines, greater N2O production may intensify global warming, as N2O is about 310 times more effective at trapping heat than CO2 (see Ch. 2: Physical Drivers of Climate Change, Section 2.3.2).103 ,104 Production of hydrogen sulfide (H2S, which is highly toxic) and intensified phosphorus recycling can occur at low oxygen levels.105 Other feedbacks may emerge as oxygen minimum zone (OMZ) shoaling diminishes the depths of diurnal vertical migrations by fish and invertebrates, and as their huge biomass and associated oxygen consumption deplete oxygen.106
13.4.4 Past Trends
Over hundreds of millions of years, oxygen has varied dramatically in the atmosphere and ocean and has been linked to biodiversity gains and losses.107 ,108 Variation in oxygenation in the paleo record is very sensitive to climate—with clear links to temperature and often CO2 variation.109 OMZs expand and contract in synchrony with warming and cooling events, respectively.110 Episodic climate events that involve rapid temperature increases over decades, followed by a cool period lasting a few hundred years, lead to major fluctuations in the intensity of Pacific and Indian Ocean OMZs (i.e., DO of < 20 µM). These events are associated with rapid variations in North Atlantic deep water formation.111 Ocean oxygen fluctuates on glacial-interglacial timescales of thousands of years in the Eastern Pacific.112 ,113
13.4.5 Modern Observations (last 50+ years)
Long-term oxygen records made over the last 50 years reflect oxygen declines in inland seas,114 ,115 ,116 in estuaries,117 ,118 and in coastal waters.119 ,120 ,121 ,122 The number of coastal, eutrophication-induced hypoxic sites in the United States has grown dramatically over the past 40 years.123 Over larger scales, global syntheses show hypoxic waters have expanded by 4.5 million km2 at a depth of 200 m,95 with widespread loss of oxygen in the Southern Ocean,94 Western Pacific,124 and North Atlantic.125 Overall oxygen declines have been greater in coastal oceans than in the open ocean126 and often greater inshore than offshore.127 The emergence of a deoxygenation signal in regions with naturally high oxygen variability will unfold over longer time periods (20–50 years from now).128
13.4.6 Projected Changes
GLOBAL MODELS
Global models generally agree that ocean deoxygenation is occurring; this finding is also reflected in in situ observations from past 50 years. Compilations of 10 Earth System models predict a global average loss of oxygen of −3.5% (higher scenario, RCP8.5) to −2.4% (lower scenario, RCP4.5) by 2100, but much stronger losses regionally, and in intermediate and mode waters (Figure 13.6).24 The North Pacific, North Atlantic, Southern Ocean, subtropical South Pacific, and South Indian Oceans all are expected to experience deoxygenation, with O2 decreases of as much as 17% in the North Pacific by 2100 for the RCP8.5 pathway. However, the tropical Atlantic and tropical Indian Oceans show increasing O2 concentrations. In the many areas where oxygen is declining, high natural variability makes it difficult to identify anthropogenically forced trends.128
REGIONAL MODELS
Regional models are critical because many oxygen drivers are local, influenced by bathymetry, winds, circulation, and fresh water and nutrient inputs. Most eastern boundary upwelling areas are predicted to experience intensified upwelling to 2100,61 although on the West Coast projections for increasing upwelling for the northern California Current occur only north of San Francisco (see Section 13.2.3).
Particularly notable for the western United States, variation in trade winds in the eastern Pacific Ocean can affect nutrient inputs, leading to centennial periods of oxygen decline or oxygen increase distinct from global oxygen decline.129 Oxygen dynamics in the Eastern Tropical Pacific are highly sensitive to equatorial circulation changes.130
Regional modeling also shows that year-to-year variability in precipitation in the central United States affects the nitrate–N flux by the Mississippi River and the extent of hypoxia in the Gulf of Mexico.131 A host of climate influences linked to warming and increased precipitation are predicted to lower dissolved oxygen in Chesapeake Bay.132
13.5: Other Coastal Changes
13.5.1 Sea Level Rise
Sea level is an important variable that affects coastal ecosystems. Global sea level rose rapidly at the end of the last glaciation, as glaciers and the polar ice sheets thinned and melted at their fringes. On average around the globe, sea level is estimated to have risen at rates exceeding 2.5 mm/year between about 8,000 and 6,000 years before present. These rates steadily decreased to less than 2.0 mm/year through about 4,000 years ago and stabilized at less than 0.4 mm/year through the late 1800s. Global sea level rise has accelerated again within the last 100 years, and now averages about 1 to 2 mm/year.133 See Chapter 12: Sea Level Rise for more thorough analysis of how sea level rise has already and will affect the U.S. coasts.
13.5.2 Wet and Dry Deposition
Dust transported from continental desert regions to the marine environment deposits nutrients such as iron, nitrogen, phosphorus, and trace metals that stimulate growth of phytoplankton and increase marine productivity.134 U.S. continental and coastal regions experience large dust deposition fluxes originating from the Saharan desert to the East and from Central Asia and China to the Northwest.135 Changes in drought frequency or intensity resulting from anthropogenically forced climate change, as well as other anthropogenic activities such as agricultural practices and land-use changes may play an important role in the future viability and strength of these dust sources (e.g., Mulitza et al. 2010136 ).
Additionally, oxidized nitrogen, released during high-temperature combustion over land, and reduced nitrogen, released from intensive agriculture, are emitted in high population areas in North America and are carried away and deposited through wet or dry deposition over coastal and open ocean ecosystems via local wind circulation. Wet deposition of pollutants produced in urban areas is known to play an important role in changes of ecosystem structure in coastal and open ocean systems through intermediate changes in the biogeochemistry, for instance in dissolved oxygen or various forms of carbon.137
13.5.3 Primary Productivity
Marine phytoplankton represent about half of the global net primary production (NPP) (approximately 50 ± 28 GtC /year), fixing atmospheric CO2 into a bioavailable form for utilization by higher trophic levels (see also Ch. 2: Physical Drivers of Climate Change).138 ,139 As such, NPP represents a critical component in the role of the oceans in climate feedback. The effect of climate change on primary productivity varies across the coasts depending on local conditions. For instance, nutrients that stimulate phytoplankton growth are impacted by various climate conditions, such as increased stratification which limits the transport of nutrient-rich deep water to the surface, changes in circulation leading to variability in dry and wet deposition of nutrients to coasts, and altered precipitation/evaporation which changes runoff of nutrients from coastal communities. The effect of the multiple physical factors on NPP is complex and leads to model uncertainties.140 There is considerable variation in model projections for NPP, from estimated decreases or no changes, to the potential increases by 2100.141 ,142 ,143 Simulations from nine Earth system models projected total NPP in 2090 to decrease by 2%–16% and export production (that is, particulate flux to the deep ocean) to drop by 7%–18% as compared to 1990 (RCP8.5).142 More information on phytoplankton species response and associated ecosystem dynamics is needed as any reduction of NPP and the associated export production would have an impact on carbon cycling and marine ecosystems.
13.5.4 Estuaries
Estuaries are critical ecosystems of biological, economic, and social importance in the United States. They are highly dynamic, influenced by the interactions of atmospheric, freshwater, terrestrial, oceanic, and benthic components. Of the 28 national estuarine research reserves in the United States and Puerto Rico, all are being impacted by climate change to varying levels.144 In particular, sea level rise, saltwater intrusion, and the degree of freshwater discharge influence the forces and processes within these estuaries.145 Sea level rise and subsidence are leading to drowning of existing salt marshes and/or subsequent changes in the relative area of the marsh plain, if adaptive upslope movement is impeded due to urbanization along shorelines. Several model scenarios indicate a decline in salt marsh habitat quality and an accelerated degradation as the rate of sea level rise increases in the latter half of the century.146 ,147 The increase in sea level as well as alterations to oceanic and atmospheric circulation can result in extreme wave conditions and storm surges, impacting coastal communities.144 Additional climate change impacts to the physical and chemical estuarine processes include more extreme sea surface temperatures (higher highs and lower lows compared to the open ocean due to shallower depths and influence from land temperatures), changes in flow rates due to changes in precipitation, and potentially greater extents of salinity intrusion.
References
- Abraham, J. P. et al., 2013: A review of global ocean temperature observations: Implications for ocean heat content estimates and climate change. Reviews of Geophysics, 51, 450–483, doi:10.1002/rog.20022. ↩
- Altieri, A. H., and K. B. Gedan, 2015: Climate change and dead zones. Global Change Biology, 21, 1395–1406, doi:10.1111/gcb.12754. ↩
- Astor, Y. M., L. Lorenzoni, R. Thunell, R. Varela, F. Muller-Karger, L. Troccoli, G. T. Taylor, M. I. Scranton, E. Tappa, and D. Rueda, 2013: Interannual variability in sea surface temperature and f CO 2 changes in the Cariaco Basin. Deep Sea Research Part II: Topical Studies in Oceanography, 93, 33–43, doi:10.1016/j.dsr2.2013.01.002. ↩
- Baden, S. P., L. O. Loo, L. Pihl, and R. Rosenberg, 1990: Effects of eutrophication on benthic communities including fish — Swedish west coast. Ambio, 19, 113–122. URL ↩
- Bakun, A., B. A. Black, S. J. Bograd, M. García-Reyes, A. J. Miller, R. R. Rykaczewski, and W. J. Sydeman, 2015: Anticipated effects of climate change on coastal upwelling ecosystems. Current Climate Change Reports, 1, 85–93, doi:10.1007/s40641-015-0008-4. ↩
- Bates, N. R., Y. M. Astor, M. J. Church, K. Currie, J. E. Dore, M. González-Dávila, L. Lorenzoni, F. Muller-Karger, J. Olafsson, and J. M. Santana-Casiano, 2014: A time-series view of changing ocean chemistry due to ocean uptake of anthropogenic CO2 and ocean acidification. Oceanography, 27, 126–141, doi:10.5670/oceanog.2014.16. ↩
- Bates, N. R., and J. T. Mathis, 2009: The Arctic Ocean marine carbon cycle: Evaluation of air-sea CO 2 exchanges, ocean acidification impacts and potential feedbacks. Biogeosciences, 6, 2433–2459, doi:10.5194/bg-6-2433-2009. ↩
- Bianchi, D., E. D. Galbraith, D. A. Carozza, K. A. S. Mislan, and C. A. Stock, 2013: Intensification of open-ocean oxygen depletion by vertically migrating animals. Nature Geoscience, 6, 545–548, doi:10.1038/ngeo1837. ↩
- Boetius, A., and F. Wenzhofer, 2013: Seafloor oxygen consumption fuelled by methane from cold seeps. Nature Geoscience, 6, 725–734, doi:10.1038/ngeo1926. ↩
- Bograd, S. J., M. P. Buil, E. D. Lorenzo, C. G. Castro, I. D. Schroeder, R. Goericke, C. R. Anderson, C. Benitez-Nelson, and F. A. Whitney, 2015: Changes in source waters to the Southern California Bight. Deep Sea Research Part II: Topical Studies in Oceanography, 112, 42–52, doi:10.1016/j.dsr2.2014.04.009. ↩
- Bond, N. A., M. F. Cronin, H. Freeland, and N. Mantua, 2015: Causes and impacts of the 2014 warm anomaly in the NE Pacific. Geophysical Research Letters, 42, 3414–3420, doi:10.1002/2015GL063306. ↩
- Booth, J. A. T., E. E. McPhee-Shaw, P. Chua, E. Kingsley, M. Denny, R. Phillips, S. J. Bograd, L. D. Zeidberg, and W. F. Gilly, 2012: Natural intrusions of hypoxic, low pH water into nearshore marine environments on the California coast. Continental Shelf Research, 45, 108–115, doi:10.1016/j.csr.2012.06.009. ↩
- Bopp, L., L. Resplandy, J. C. Orr, S. C. Doney, J. P. Dunne, M. Gehlen, P. Halloran, C. Heinze, T. Ilyina, R. Séférian, J. Tjiputra, and M. Vichi, 2013: Multiple stressors of ocean ecosystems in the 21st century: Projections with CMIP5 models. Biogeosciences, 10, 6225–6245, doi:10.5194/bg-10-6225-2013. ↩
- Borges, A. V., and N. Gypens, 2010: Carbonate chemistry in the coastal zone responds more strongly to eutrophication than ocean acidification. Limnology and Oceanography, 55, 346–353, doi:10.4319/lo.2010.55.1.0346. ↩
- Boyer, T., C. M. Domingues, S. A. Good, G. C. Johnson, J. M. Lyman, M. Ishii, V. Gouretski, J. K. Willis, J. Antonov, S. Wijffels, J. A. Church, R. Cowley, and N. L. Bindoff, 2016: Sensitivity of global upper-ocean heat content estimates to mapping methods, XBT bias corrections, and baseline climatologies. Journal of Climate, 29, 4817–4842, doi:10.1175/jcli-d-15-0801.1. ↩
- Brady, R. X., M. A. Alexander, N. S. Lovenduski, and R. R. Rykaczewski, 2017: Emergent anthropogenic trends in California Current upwelling. Geophysical Research Letters, 44, 5044–5052, doi:10.1002/2017GL072945. ↩
- Breitburg, D. L., J. Salisbury, J. M. Bernhard, W.-J. Cai, S. Dupont, S. C. Doney, K. J. Kroeker, L. A. Levin, W. C. Long, L. M. Milke, S. H. Miller, B. Phelan, U. Passow, B. A. Seibel, A. E. Todgham, and A. M. Tarrant, 2015: And on top of all that… Coping with ocean acidification in the midst of many stressors. Oceanography, 28, 48–61, doi:10.5670/oceanog.2015.31. ↩
- Brush, G. S., 2009: Historical land use, nitrogen, and coastal eutrophication: A paleoecological perspective. Estuaries and Coasts, 32, 18–28, doi:10.1007/s12237-008-9106-z. ↩
- Bryden, H. L., B. A. King, and G. D. McCarthy, 2011: South Atlantic overturning circulation at 24°S. Journal of Marine Research, 69, 38–55, doi:10.1357/002224011798147633. ↩
- Bryden, H. L., H. R. Longworth, and S. A. Cunningham, 2005: Slowing of the Atlantic meridional overturning circulation at 25°N. Nature, 438, 655–657, doi:10.1038/nature04385. ↩
- Buckley, M. W., and J. Marshall, 2016: Observations, inferences, and mechanisms of the Atlantic Meridional Overturning Circulation: A review. Reviews of Geophysics, 54, 5–63, doi:10.1002/2015RG000493. ↩
- Böning, C. W., E. Behrens, A. Biastoch, K. Getzlaff, and J. L. Bamber, 2016: Emerging impact of Greenland meltwater on deepwater formation in the North Atlantic Ocean. Nature Geoscience, 9, 523–527, doi:10.1038/ngeo2740. ↩
- Caldeira, K., and M. E. Wickett, 2005: Ocean model predictions of chemistry changes from carbon dioxide emissions to the atmosphere and ocean. Journal of Geophysical Research: Oceans, 110, C09S04, doi:10.1029/2004JC002671. ↩
- Carr, M.-E. et al., 2006: A comparison of global estimates of marine primary production from ocean color. Deep Sea Research Part II: Topical Studies in Oceanography, 53, 741–770, doi:10.1016/j.dsr2.2006.01.028. ↩
- Chavez, F. P., M. Messié, and J. T. Pennington, 2011: Marine primary production in relation to climate variability and change. Annual Review of Marine Science, 3, 227–260, doi:10.1146/annurev.marine.010908.163917. ↩
- Cheng, L., K. E. Trenberth, J. Fasullo, T. Boyer, J. Abraham, and J. Zhu, 2017: Improved estimates of ocean heat content from 1960 to 2015. Science Advances, 3, e1601545, doi:10.1126/sciadv.1601545. ↩
- Cheng, W., J. C. H. Chiang, and D. Zhang, 2013: Atlantic Meridional Overturning Circulation (AMOC) in CMIP5 models: RCP and historical simulations. Journal of Climate, 26, 7187–7197, doi:10.1175/jcli-d-12-00496.1. ↩
- Chiapello, I., 2014: Dust observations and climatology. P. Knippertz and J.-B.W. Stuut, Eds., Springer Netherlands, 149–177. ↩
- Ciais, P., C. Sabine, G. Bala, L. Bopp, V. Brovkin, J. Canadell, A. Chhabra, R. DeFries, J. Galloway, M. Heimann, C. Jones, C. Le Quéré, R. B. Myneni, S. Piao, and P. Thornton, 2013: Carbon and other biogeochemical cycles. T.F. Stocker, D. Qin, G.-K. Plattner, M. Tignor, S.K. Allen, J. Boschung, A. Nauels, Y. Xia, V. Bex, and P.M. Midgley, Eds., Cambridge University Press, 465–570. URL ↩
- Codispoti, L. A., J. A. Brandes, J. P. Christensen, A. H. Devol, S. W. A. Naqvi, H. W. Paerl, and T. Yoshinari, 2001: The oceanic fixed nitrogen and nitrous oxide budgets: Moving targets as we enter the anthropocene? Scientia Marina, 65, 85–105, doi:10.3989/scimar.2001.65s285. ↩
- Collins, M., R. Knutti, J. Arblaster, J.-L. Dufresne, T. Fichefet, P. Friedlingstein, X. Gao, W. J. Gutowski, T. Johns, G. Krinner, M. Shongwe, C. Tebaldi, A. J. Weaver, and M. Wehner, 2013: Long-term climate change: Projections, commitments and irreversibility. T.F. Stocker, D. Qin, G.-K. Plattner, M. Tignor, S.K. Allen, J. Boschung, A. Nauels, Y. Xia, V. Bex, and P.M. Midgley, Eds., Cambridge University Press, 1029–1136. URL ↩
- Conley, D. J., J. Carstensen, J. Aigars, P. Axe, E. Bonsdorff, T. Eremina, B.-M. Haahti, C. Humborg, P. Jonsson, J. Kotta, C. Lännegren, U. Larsson, A. Maximov, M. R. Medina, E. Lysiak-Pastuszak, N. Remeikaitė-Nikienė, J. Walve, S. Wilhelms, and L. Zillén, 2011: Hypoxia is increasing in the coastal zone of the Baltic Sea. Environmental Science & Technology, 45, 6777–6783, doi:10.1021/es201212r. ↩
- Deutsch, C., H. Brix, T. Ito, H. Frenzel, and L. Thompson, 2011: Climate-forced variability of ocean hypoxia. Science, 333, 336–339, doi:10.1126/science.1202422. ↩
- Deutsch, C., W. Berelson, R. Thunell, T. Weber, C. Tems, J. McManus, J. Crusius, T. Ito, T. Baumgartner, V. Ferreira, J. Mey, and A. van Geen, 2014: Centennial changes in North Pacific anoxia linked to tropical trade winds. Science, 345, 665–668, doi:10.1126/science.1252332. ↩
- Diaz, R. J., and R. Rosenberg, 2008: Spreading dead zones and consequences for marine ecosystems. Science, 321, 926–929, doi:10.1126/science.1156401. ↩
- Doney, S. C., N. Mahowald, I. Lima, R. A. Feely, F. T. Mackenzie, J. F. Lamarque, and P. J. Rasch, 2007: Impact of anthropogenic atmospheric nitrogen and sulfur deposition on ocean acidification and the inorganic carbon system. Proceedings of the National Academy of Sciences, 104, 14580–14585, doi:10.1073/pnas.0702218104. ↩
- Dong, S., G. Goni, and F. Bringas, 2015: Temporal variability of the South Atlantic Meridional Overturning Circulation between 20°S and 35°S. Geophysical Research Letters, 42, 7655–7662, doi:10.1002/2015GL065603. ↩
- Donner, S. D., and D. Scavia, 2007: How climate controls the flux of nitrogen by the Mississippi River and the development of hypoxia in the Gulf of Mexico. Limnology and Oceanography, 52, 856–861, doi:10.4319/lo.2007.52.2.0856. ↩
- Drijfhout, S. S., S. L. Weber, and E. van der Swaluw, 2011: The stability of the MOC as diagnosed from model projections for pre-industrial, present and future climates. Climate Dynamics, 37, 1575–1586, doi:10.1007/s00382-010-0930-z. ↩
- Duarte, C. M., I. E. Hendriks, T. S. Moore, Y. S. Olsen, A. Steckbauer, L. Ramajo, J. Carstensen, J. A. Trotter, and M. McCulloch, 2013: Is ocean acidification an open-ocean syndrome? Understanding anthropogenic impacts on seawater pH. Estuaries and Coasts, 36, 221–236, doi:10.1007/s12237-013-9594-3. ↩
- Durack, P. J., and S. E. Wijffels, 2010: Fifty-year trends in global ocean salinities and their relationship to broad-scale warming. Journal of Climate, 23, 4342–4362, doi:10.1175/2010jcli3377.1. ↩
- EPA, 2017: Inventory of U.S. Greenhouse Gas Emissions and Sinks: 1990-2015. 633 pp., U.S. Environmental Protection Agency. URL ↩
- Evans, W., J. T. Mathis, and J. N. Cross, 2014: Calcium carbonate corrosivity in an Alaskan inland sea. Biogeosciences, 11, 365–379, doi:10.5194/bg-11-365-2014. ↩
- Falkowski, P. G., T. Algeo, L. Codispoti, C. Deutsch, S. Emerson, B. Hales, R. B. Huey, W. J. Jenkins, L. R. Kump, L. A. Levin, T. W. Lyons, N. B. Nelson, O. S. Schofield, R. Summons, L. D. Talley, E. Thomas, F. Whitney, and C. B. Pilcher, 2011: Ocean deoxygenation: Past, present, and future. Eos, Transactions, American Geophysical Union, 92, 409–410, doi:10.1029/2011EO460001. ↩
- Feely, R. A., C. L. Sabine, J. M. Hernandez-Ayon, D. Ianson, and B. Hales, 2008: Evidence for upwelling of corrosive “acidified” water onto the continental shelf. Science, 320, 1490–1492, doi:10.1126/science.1155676. ↩
- Feely, R. A., C. L. Sabine, K. Lee, W. Berelson, J. Kleypas, V. J. Fabry, and F. J. Millero, 2004: Impact of anthropogenic CO 2 on the CaCO 3 system in the oceans. Science, 305, 362–366, doi:10.1126/science.1097329. ↩
- Feely, R. A., S. C. Doney, and S. R. Cooley, 2009: Ocean acidification: Present conditions and future changes in a high-CO2 world. Oceanography, 22, 36–47, doi:10.5670/oceanog.2009.95. ↩
- Feely, R. A., S. R. Alin, B. Carter, N. Bednaršek, B. Hales, F. Chan, T. M. Hill, B. Gaylord, E. Sanford, R. H. Byrne, C. L. Sabine, D. Greeley, and L. Juranek, 2016: Chemical and biological impacts of ocean acidification along the west coast of North America. Estuarine, Coastal and Shelf Science, 183, Part A, 260–270, doi:10.1016/j.ecss.2016.08.043. ↩
- Franz, B. A., M. J. Behrenfeld, D. A. Siegel, and S. R. Signorini, 2016: Global ocean phytoplankton [in “State of the Climate in 2015”]. Bulletin of the American Meteorological Society, 97, S87–S89, doi:10.1175/2016BAMSStateoftheClimate.1. ↩
- Friedrich, T., A. Timmermann, A. Abe-Ouchi, N. R. Bates, M. O. Chikamoto, M. J. Church, J. E. Dore, D. K. Gledhill, M. Gonzalez-Davila, M. Heinemann, T. Ilyina, J. H. Jungclaus, E. McLeod, A. Mouchet, and J. M. Santana-Casiano, 2012: Detecting regional anthropogenic trends in ocean acidification against natural variability. Nature Climate Change, 2, 167–171, doi:10.1038/nclimate1372. ↩
- Frölicher, T. L., K. B. Rodgers, C. A. Stock, and W. W. L. Cheung, 2016: Sources of uncertainties in 21st century projections of potential ocean ecosystem stressors. Global Biogeochemical Cycles, 30, 1224–1243, doi:10.1002/2015GB005338. ↩
- Fu, W., J. T. Randerson, and J. K. Moore, 2016: Climate change impacts on net primary production (NPP) and export production (EP) regulated by increasing stratification and phytoplankton community structure in the CMIP5 models. Biogeosciences, 13, 5151–5170, doi:10.5194/bg-13-5151-2016. ↩
- Galbraith, E. D., M. Kienast, T. F. Pedersen, and S. E. Calvert, 2004: Glacial-interglacial modulation of the marine nitrogen cycle by high-latitude O2 supply to the global thermocline. Paleoceanography, 19, PA4007, doi:10.1029/2003PA001000. ↩
- García-Reyes, M., W. J. Sydeman, D. S. Schoeman, R. R. Rykaczewski, B. A. Black, A. J. Smit, and S. J. Bograd, 2015: Under pressure: Climate change, upwelling, and eastern boundary upwelling ecosystems. Frontiers in Marine Science, 2, Art. 109, doi:10.3389/fmars.2015.00109. ↩
- Garzoli, S. L., M. O. Baringer, S. Dong, R. C. Perez, and Q. Yao, 2013: South Atlantic meridional fluxes. Deep Sea Research Part I: Oceanographic Research Papers, 71, 21–32, doi:10.1016/j.dsr.2012.09.003. ↩
- Gattuso, J.-P. et al., 2015: Contrasting futures for ocean and society from different anthropogenic CO 2 emissions scenarios. Science, 349, aac4722, doi:10.1126/science.aac4722. ↩
- Gilbert, D., B. Sundby, C. Gobeil, A. Mucci, and G.-H. Tremblay, 2005: A seventy-two-year record of diminishing deep-water oxygen in the St. Lawrence estuary: The northwest Atlantic connection. Limnology and Oceanography, 50, 1654–1666, doi:10.4319/lo.2005.50.5.1654. ↩
- Gilbert, D., N. N. Rabalais, R. J. Díaz, and J. Zhang, 2010: Evidence for greater oxygen decline rates in the coastal ocean than in the open ocean. Biogeosciences, 7, 2283–2296, doi:10.5194/bg-7-2283-2010. ↩
- Gledhill, D. K. et al., 2015: Ocean and coastal acidification off New England and Nova Scotia. Oceanography, 28, 182–197, doi:10.5670/oceanog.2015.41. ↩
- Gobler, C. J., E. L. DePasquale, A. W. Griffith, and H. Baumann, 2014: Hypoxia and acidification have additive and synergistic negative effects on the growth, survival, and metamorphosis of early life stage bivalves. PLoS ONE, 9, e83648, doi:10.1371/journal.pone.0083648. ↩
- Gruber, N., 2008: Chapter 1 - The marine nitrogen cycle: Overview and challenges. Academic Press, 1–50. ↩
- Halloran, P. R., B. B. B. Booth, C. D. Jones, F. H. Lambert, D. J. McNeall, I. J. Totterdell, and C. Völker, 2015: The mechanisms of North Atlantic CO 2 uptake in a large Earth System Model ensemble. Biogeosciences, 12, 4497–4508, doi:10.5194/bg-12-4497-2015. ↩
- Harris, K. E., M. D. DeGrandpre, and B. Hales, 2013: Aragonite saturation state dynamics in a coastal upwelling zone. Geophysical Research Letters, 40, 2720–2725, doi:10.1002/grl.50460. ↩
- Helm, K. P., N. L. Bindoff, and J. A. Church, 2011: Observed decreases in oxygen content of the global ocean. Geophysical Research Letters, 38, L23602, doi:10.1029/2011GL049513. ↩
- Hendriks, I. E., C. M. Duarte, Y. S. Olsen, A. Steckbauer, L. Ramajo, T. S. Moore, J. A. Trotter, and M. McCulloch, 2015: Biological mechanisms supporting adaptation to ocean acidification in coastal ecosystems. Estuarine, Coastal and Shelf Science, 152, A1–A8, doi:10.1016/j.ecss.2014.07.019. ↩
- Henson, S. A., C. Beaulieu, and R. Lampitt, 2016: Observing climate change trends in ocean biogeochemistry: When and where. Global Change Biology, 22, 1561–1571, doi:10.1111/gcb.13152. ↩
- Henson, S. A., J. L. Sarmiento, J. P. Dunne, L. Bopp, I. Lima, S. C. Doney, J. John, and C. Beaulieu, 2010: Detection of anthropogenic climate change in satellite records of ocean chlorophyll and productivity. Biogeosciences, 7, 621–640, doi:10.5194/bg-7-621-2010. ↩
- Hoegh-Guldberg, O., R. Cai, E. S. Poloczanska, P. G. Brewer, S. Sundby, K. Hilmi, V. J. Fabry, and S. Jung, 2014: The Ocean--Supplementary material. V.R. Barros, C.B. Field, D.J. Dokken, M.D. Mastrandrea, K.J. Mach, T.E. Bilir, M. Chatterjee, K.L. Ebi, Y.O. Estrada, R.C. Genova, B. Girma, E.S. Kissel, A.N. Levy, S. MacCracken, P.R. Mastrandrea, and L.L. White, Eds., Cambridge University Press, 1655–1731. URL ↩
- Huang, B., V. F. Banzon, E. Freeman, J. Lawrimore, W. Liu, T. C. Peterson, T. M. Smith, P. W. Thorne, S. D. Woodruff, and H.-M. Zhang, 2015: Extended Reconstructed Sea Surface Temperature Version 4 (ERSST.v4). Part I: Upgrades and intercomparisons. Journal of Climate, 28, 911–930, doi:10.1175/JCLI-D-14-00006.1. ↩
- Hönisch, B. et al., 2012: The geological record of ocean acidification. Science, 335, 1058–1063, doi:10.1126/science.1208277. ↩
- Ito, T., A. Nenes, M. S. Johnson, N. Meskhidze, and C. Deutsch, 2016: Acceleration of oxygen decline in the tropical Pacific over the past decades by aerosol pollutants. Nature Geoscience, 9, 443–447, doi:10.1038/ngeo2717. ↩
- Jackson, L. C., K. A. Peterson, C. D. Roberts, and R. A. Wood, 2016: Recent slowing of Atlantic overturning circulation as a recovery from earlier strengthening. Nature Geoscience, 9, 518–522, doi:10.1038/ngeo2715. ↩
- Jacox, M. G., A. M. Moore, C. A. Edwards, and J. Fiechter, 2014: Spatially resolved upwelling in the California Current System and its connections to climate variability. Geophysical Research Letters, 41, 3189–3196, doi:10.1002/2014GL059589. ↩
- Jiang, L.-Q., R. A. Feely, B. R. Carter, D. J. Greeley, D. K. Gledhill, and K. M. Arzayus, 2015: Climatological distribution of aragonite saturation state in the global oceans. Global Biogeochemical Cycles, 29, 1656–1673, doi:10.1002/2015GB005198. ↩
- Jickells, T., and C. M. Moore, 2015: The importance of atmospheric deposition for ocean productivity. Annual Review of Ecology, Evolution, and Systematics, 46, 481–501, doi:10.1146/annurev-ecolsys-112414-054118. ↩
- Johns, W. E., M. O. Baringer, L. M. Beal, S. A. Cunningham, T. Kanzow, H. L. Bryden, J. J. M. Hirschi, J. Marotzke, C. S. Meinen, B. Shaw, and R. Curry, 2011: Continuous, array-based estimates of Atlantic ocean heat transport at 26.5°N. Journal of Climate, 24, 2429–2449, doi:10.1175/2010jcli3997.1. ↩
- Justić, D., T. Legović, and L. Rottini-Sandrini, 1987: Trends in oxygen content 1911–1984 and occurrence of benthic mortality in the northern Adriatic Sea. Estuarine, Coastal and Shelf Science, 25, 435–445, doi:10.1016/0272-7714(87)90035-7. ↩
- Kanzow, T., S. A. Cunningham, W. E. Johns, J. J.-M. Hirschi, J. Marotzke, M. O. Baringer, C. S. Meinen, M. P. Chidichimo, C. Atkinson, L. M. Beal, H. L. Bryden, and J. Collins, 2010: Seasonal variability of the Atlantic meridional overturning circulation at 26.5°N. Journal of Climate, 23, 5678–5698, doi:10.1175/2010jcli3389.1. ↩
- Knoll, A. H., and S. B. Carroll, 1999: Early animal evolution: Emerging views from comparative biology and geology. Science, 284, 2129–2137, doi:10.1126/science.284.5423.2129. ↩
- Kosaka, Y., and S.-P. Xie, 2013: Recent global-warming hiatus tied to equatorial Pacific surface cooling. Nature, 501, 403–407, doi:10.1038/nature12534. ↩
- Laufkötter, C. et al., 2015: Drivers and uncertainties of future global marine primary production in marine ecosystem models. Biogeosciences, 12, 6955–6984, doi:10.5194/bg-12-6955-2015. ↩
- Le Quéré, C. et al., 2016: Global carbon budget 2016. Earth System Science Data, 8, 605–649, doi:10.5194/essd-8-605-2016. ↩
- Lee, M., E. Shevliakova, S. Malyshev, P. C. D. Milly, and P. R. Jaffé, 2016: Climate variability and extremes, interacting with nitrogen storage, amplify eutrophication risk. Geophysical Research Letters, 43, 7520–7528, doi:10.1002/2016GL069254. ↩
- Lee, S.-K., W. Park, M. O. Baringer, A. L. Gordon, B. Huber, and Y. Liu, 2015: Pacific origin of the abrupt increase in Indian Ocean heat content during the warming hiatus. Nature Geoscience, 8, 445–449, doi:10.1038/ngeo2438. ↩
- Levitus, S., J. I. Antonov, T. P. Boyer, O. K. Baranova, H. E. Garcia, R. A. Locarnini, A. V. Mishonov, J. R. Reagan, D. Seidov, E. S. Yarosh, and M. M. Zweng, 2012: World ocean heat content and thermosteric sea level change (0–2000 m), 1955–2010. Geophysical Research Letters, 39, L10603, doi:10.1029/2012GL051106. ↩
- Liu, W., S.-P. Xie, Z. Liu, and J. Zhu, 2017: Overlooked possibility of a collapsed Atlantic Meridional Overturning Circulation in warming climate. Science Advances, 3, e1601666, doi:10.1126/sciadv.1601666. ↩
- Llovel, W., J. K. Willis, F. W. Landerer, and I. Fukumori, 2014: Deep-ocean contribution to sea level and energy budget not detectable over the past decade. Nature Climate Change, 4, 1031–1035, doi:10.1038/nclimate2387. ↩
- Long, M. C., C. Deutsch, and T. Ito, 2016: Finding forced trends in oceanic oxygen. Global Biogeochemical Cycles, 30, 381–397, doi:10.1002/2015GB005310. ↩
- Longworth, H. R., H. L. Bryden, and M. O. Baringer, 2011: Historical variability in Atlantic meridional baroclinic transport at 26.5°N from boundary dynamic height observations. Deep Sea Research Part II: Topical Studies in Oceanography, 58, 1754–1767, doi:10.1016/j.dsr2.2010.10.057. ↩
- Manzello, D., I. Enochs, S. Musielewicz, R. Carlton, and D. Gledhill, 2013: Tropical cyclones cause CaCO3 undersaturation of coral reef seawater in a high-CO2 world. Journal of Geophysical Research Oceans, 118, 5312–5321, doi:10.1002/jgrc.20378. ↩
- Mathis, J. T., S. R. Cooley, N. Lucey, S. Colt, J. Ekstrom, T. Hurst, C. Hauri, W. Evans, J. N. Cross, and R. A. Feely, 2015: Ocean acidification risk assessment for Alaska’s fishery sector. Progress in Oceanography, 136, 71–91, doi:10.1016/j.pocean.2014.07.001. ↩
- Matthews, J. B. R., 2013: Comparing historical and modern methods of sea surface temperature measurement – Part 1: Review of methods, field comparisons and dataset adjustments. Ocean Science, 9, 683–694, doi:10.5194/os-9-683-2013. ↩
- McDonagh, E. L., B. A. King, H. L. Bryden, P. Courtois, Z. Szuts, M. Baringer, S. A. Cunningham, C. Atkinson, and G. McCarthy, 2015: Continuous estimate of Atlantic oceanic freshwater flux at 26.5°N. Journal of Climate, 28, 8888–8906, doi:10.1175/jcli-d-14-00519.1. ↩
- McFall-Ngai, M. et al., 2013: Animals in a bacterial world, a new imperative for the life sciences. Proceedings of the National Academy of Sciences, 110, 3229–3236, doi:10.1073/pnas.1218525110. ↩
- Mei, W., S.-P. Xie, F. Primeau, J. C. McWilliams, and C. Pasquero, 2015: Northwestern Pacific typhoon intensity controlled by changes in ocean temperatures. Science Advances, 1, e1500014, doi:10.1126/sciadv.1500014. ↩
- Mills, K. E., A. J. Pershing, C. J. Brown, Y. Chen, F.-S. Chiang, D. S. Holland, S. Lehuta, J. A. Nye, J. C. Sun, A. C. Thomas, and R. A. Wahle, 2013: Fisheries management in a changing climate: Lessons from the 2012 ocean heat wave in the Northwest Atlantic. Oceanography, 26 (2), 191–195, doi:10.5670/oceanog.2013.27. ↩
- Moffitt, S. E., R. A. Moffitt, W. Sauthoff, C. V. Davis, K. Hewett, and T. M. Hill, 2015: Paleoceanographic insights on recent oxygen minimum zone expansion: Lessons for modern oceanography. PLoS ONE, 10, e0115246, doi:10.1371/journal.pone.0115246. ↩
- Monbaliu, J., Z. Chen, D. Felts, J. Ge, F. Hissel, J. Kappenberg, S. Narayan, R. J. Nicholls, N. Ohle, D. Schuster, J. Sothmann, and P. Willems, 2014: Risk assessment of estuaries under climate change: Lessons from Western Europe. Coastal Engineering, 87, 32–49, doi:10.1016/j.coastaleng.2014.01.001. ↩
- Montes, I., B. Dewitte, E. Gutknecht, A. Paulmier, I. Dadou, A. Oschlies, and V. Garçon, 2014: High-resolution modeling of the eastern tropical Pacific oxygen minimum zone: Sensitivity to the tropical oceanic circulation. Journal of Geophysical Research Oceans, 119, 5515–5532, doi:10.1002/2014JC009858. ↩
- Mulitza, S., D. Heslop, D. Pittauerova, H. W. Fischer, I. Meyer, J.-B. Stuut, M. Zabel, G. Mollenhauer, J. A. Collins, H. Kuhnert, and M. Schulz, 2010: Increase in African dust flux at the onset of commercial agriculture in the Sahel region. Nature, 466, 226–228, doi:10.1038/nature09213. ↩
- Najjar, R. G., C. R. Pyke, M. B. Adams, D. Breitburg, C. Hershner, M. Kemp, R. Howarth, M. R. Mulholland, M. Paolisso, D. Secor, K. Sellner, D. Wardrop, and R. Wood, 2010: Potential climate-change impacts on the Chesapeake Bay. Estuarine, Coastal and Shelf Science, 86, 1–20, doi:10.1016/j.ecss.2009.09.026. ↩
- Nieves, V., J. K. Willis, and W. C. Patzert, 2015: Recent hiatus caused by decadal shift in Indo-Pacific heating. Science, 349, 532–535, doi:10.1126/science.aaa4521. ↩
- Orr, J. C. et al., 2005: Anthropogenic ocean acidification over the twenty-first century and its impact on calcifying organisms. Nature, 437, 681–686, doi:10.1038/nature04095. ↩
- Paerl, H. W., R. L. Dennis, and D. R. Whitall, 2002: Atmospheric deposition of nitrogen: Implications for nutrient over-enrichment of coastal waters. Estuaries, 25, 677–693, doi:10.1007/bf02804899. ↩
- Patara, L., and C. W. Böning, 2014: Abyssal ocean warming around Antarctica strengthens the Atlantic overturning circulation. Geophysical Research Letters, 41, 3972–3978, doi:10.1002/2014GL059923. ↩
- Pershing, A. J., M. A. Alexander, C. M. Hernandez, L. A. Kerr, A. Le Bris, K. E. Mills, J. A. Nye, N. R. Record, H. A. Scannell, J. D. Scott, G. D. Sherwood, and A. C. Thomas, 2015: Slow adaptation in the face of rapid warming leads to collapse of the Gulf of Maine cod fishery. Science, 350, 809–812, doi:10.1126/science.aac9819. ↩
- Purkey, S. G., and G. C. Johnson, 2010: Warming of global abyssal and deep Southern Ocean waters between the 1990s and 2000s: Contributions to global heat and sea level rise budgets. Journal of Climate, 23, 6336–6351, doi:10.1175/2010JCLI3682.1. ↩
- Qi, D., L. Chen, B. Chen, Z. Gao, W. Zhong, R. A. Feely, L. G. Anderson, H. Sun, J. Chen, M. Chen, L. Zhan, Y. Zhang, and W.-J. Cai, 2017: Increase in acidifying water in the western Arctic Ocean. Nature Climate Change, 7, 195–199, doi:10.1038/nclimate3228. ↩
- Rabalais, N. N., R. E. Turner, B. K. Sen Gupta, D. F. Boesch, P. Chapman, and M. C. Murrell, 2007: Hypoxia in the northern Gulf of Mexico: Does the science support the plan to reduce, mitigate, and control hypoxia? Estuaries and Coasts, 30, 753–772, doi:10.1007/bf02841332. ↩
- Rabalais, N. N., R. E. Turner, R. J. Diaz, and D. Justic, 2009: Global change and eutrophication of coastal waters. ICES Journal of Marine Science, 66, 1528–1537, doi:10.1093/icesjms/fsp047. ↩
- Rabalais, N. N., R. J. Díaz, L. A. Levin, R. E. Turner, D. Gilbert, and J. Zhang, 2010: Dynamics and distribution of natural and human-caused hypoxia. Biogeosciences, 7, 585–619, doi:10.5194/bg-7-585-2010. ↩
- Rahmstorf, S., J. E. Box, G. Feulner, M. E. Mann, A. Robinson, S. Rutherford, and E. J. Schaffernicht, 2015: Exceptional twentieth-century slowdown in Atlantic Ocean overturning circulation. Nature Climate Change, 5, 475–480, doi:10.1038/nclimate2554. ↩
- Reay, D. S., F. Dentener, P. Smith, J. Grace, and R. A. Feely, 2008: Global nitrogen deposition and carbon sinks. Nature Geoscience, 1, 430–437, doi:10.1038/ngeo230. ↩
- Rhein, M., S. R. Rintoul, S. Aoki, E. Campos, D. Chambers, R. A. Feely, S. Gulev, G. C. Johnson, S. A. Josey, A. Kostianoy, C. Mauritzen, D. Roemmich, L. D. Talley, and F. Wang, 2013: Observations: Ocean. T.F. Stocker, D. Qin, G.-K. Plattner, M. Tignor, S.K. Allen, J. Boschung, A. Nauels, Y. Xia, V. Bex, and P.M. Midgley, Eds., Cambridge University Press, 255–316. URL ↩
- Robinson, P., A. K. Leight, D. D. Trueblood, and B. Wood, 2013: Climate sensitivity of the National Estuarine Research Reserve System. 79 pp., NERRS, NOAA National Ocean Service. URL ↩
- Robinson, R. S., A. Mix, and P. Martinez, 2007: Southern Ocean control on the extent of denitrification in the southeast Pacific over the last 70 ka. Quaternary Science Reviews, 26, 201–212, doi:10.1016/j.quascirev.2006.08.005. ↩
- Roemmich, D., J. Church, J. Gilson, D. Monselesan, P. Sutton, and S. Wijffels, 2015: Unabated planetary warming and its ocean structure since 2006. Nature Climate Change, 5, 240–245, doi:10.1038/nclimate2513. ↩
- Romanou, A., J. Marshall, M. Kelley, and J. Scott, 2017: Role of the ocean’s AMOC in setting the uptake efficiency of transient tracers. Geophysical Research Letters, 44, 5590–5598, doi:10.1002/2017GL072972. ↩
- Rossby, C.-G., 1959: Current problems in meteorology. B. Bolin, Ed., Rockefeller Institute Press, 9–50. ↩
- Rykaczewski, R. R., J. P. Dunne, W. J. Sydeman, M. García-Reyes, B. A. Black, and S. J. Bograd, 2015: Poleward displacement of coastal upwelling-favorable winds in the ocean’s eastern boundary currents through the 21st century. Geophysical Research Letters, 42, 6424–6431, doi:10.1002/2015GL064694. ↩
- Saba, V. S., S. M. Griffies, W. G. Anderson, M. Winton, M. A. Alexander, T. L. Delworth, J. A. Hare, M. J. Harrison, A. Rosati, G. A. Vecchi, and R. Zhang, 2016: Enhanced warming of the Northwest Atlantic Ocean under climate change. Journal of Geophysical Research Oceans, 121, 118–132, doi:10.1002/2015JC011346. ↩
- Salisbury, J., M. Green, C. Hunt, and J. Campbell, 2008: Coastal acidification by rivers: A threat to shellfish? Eos, Transactions, American Geophysical Union, 89, 513–513, doi:10.1029/2008EO500001. ↩
- Schile, L. M., J. C. Callaway, J. T. Morris, D. Stralberg, V. T. Parker, and M. Kelly, 2014: Modeling tidal marsh distribution with sea-level rise: Evaluating the role of vegetation, sediment, and upland habitat in marsh resiliency. PLoS ONE, 9, e88760, doi:10.1371/journal.pone.0088760. ↩
- Schmittner, A., E. D. Galbraith, S. W. Hostetler, T. F. Pedersen, and R. Zhang, 2007: Large fluctuations of dissolved oxygen in the Indian and Pacific oceans during Dansgaard–Oeschger oscillations caused by variations of North Atlantic Deep Water subduction. Paleoceanography, 22, PA3207, doi:10.1029/2006PA001384. ↩
- Skliris, N., R. Marsh, S. A. Josey, S. A. Good, C. Liu, and R. P. Allan, 2014: Salinity changes in the World Ocean since 1950 in relation to changing surface freshwater fluxes. Climate Dynamics, 43, 709–736, doi:10.1007/s00382-014-2131-7. ↩
- Smeed, D. A., G. D. McCarthy, S. A. Cunningham, E. Frajka-Williams, D. Rayner, W. E. Johns, C. S. Meinen, M. O. Baringer, B. I. Moat, A. Duchez, and H. L. Bryden, 2014: Observed decline of the Atlantic meridional overturning circulation 2004–2012. Ocean Science, 10, 29–38, doi:10.5194/os-10-29-2014. ↩
- Steinman, B. A., M. E. Mann, and S. K. Miller, 2015: Atlantic and Pacific Multidecadal Oscillations and Northern Hemisphere temperatures. Science, 347, 988–991, doi:10.1126/science.1257856. ↩
- Stendardo, I., and N. Gruber, 2012: Oxygen trends over five decades in the North Atlantic. Journal of Geophysical Research, 117, C11004, doi:10.1029/2012JC007909. ↩
- Stramma, L., S. Schmidtko, L. A. Levin, and G. C. Johnson, 2010: Ocean oxygen minima expansions and their biological impacts. Deep Sea Research Part I: Oceanographic Research Papers, 57, 587–595, doi:10.1016/j.dsr.2010.01.005. ↩
- Straneo, F., and P. Heimbach, 2013: North Atlantic warming and the retreat of Greenland’s outlet glaciers. Nature, 504, 36–43, doi:10.1038/nature12854. ↩
- Sutton, A. J., C. L. Sabine, R. A. Feely, W. J. Cai, M. F. Cronin, M. J. McPhaden, J. M. Morell, J. A. Newton, J. H. Noh, S. R. Ólafsdóttir, J. E. Salisbury, U. Send, D. C. Vandemark, and R. A. Weller, 2016: Using present-day observations to detect when anthropogenic change forces surface ocean carbonate chemistry outside preindustrial bounds. Biogeosciences, 13, 5065–5083, doi:10.5194/bg-13-5065-2016. ↩
- Swanson, K. M., J. Z. Drexler, C. C. Fuller, and D. H. Schoellhamer, 2015: Modeling tidal freshwater marsh sustainability in the Sacramento–San Joaquin delta under a broad suite of potential future scenarios. San Francisco Estuary and Watershed Science, 13, 21, doi:10.15447/sfews.2015v13iss1art3. ↩
- Sydeman, W. J., M. García-Reyes, D. S. Schoeman, R. R. Rykaczewski, S. A. Thompson, B. A. Black, and S. J. Bograd, 2014: Climate change and wind intensification in coastal upwelling ecosystems. Science, 345, 77–80, doi:10.1126/science.1251635. ↩
- Takatani, Y., D. Sasano, T. Nakano, T. Midorikawa, and M. Ishii, 2012: Decrease of dissolved oxygen after the mid-1980s in the western North Pacific subtropical gyre along the 137°E repeat section. Global Biogeochemical Cycles, 26, GB2013, doi:10.1029/2011GB004227. ↩
- Talley, L. D. et al., 2016: Changes in ocean heat, carbon content, and ventilation: A review of the first decade of GO-SHIP global repeat hydrography. Annual Review of Marine Science, 8, 185–215, doi:10.1146/annurev-marine-052915-100829. ↩
- Taylor, G. T., F. E. Muller-Karger, R. C. Thunell, M. I. Scranton, Y. Astor, R. Varela, L. T. Ghinaglia, L. Lorenzoni, K. A. Fanning, S. Hameed, and O. Doherty, 2012: Ecosystem responses in the southern Caribbean Sea to global climate change. Proceedings of the National Academy of Sciences, 109, 19315–19320, doi:10.1073/pnas.1207514109. ↩
- Thompson, P. R., B. D. Hamlington, F. W. Landerer, and S. Adhikari, 2016: Are long tide gauge records in the wrong place to measure global mean sea level rise? Geophysical Research Letters, 43, 10,403–410,411, doi:10.1002/2016GL070552. ↩
- Trenberth, K. E., J. T. Fasullo, and M. A. Balmaseda, 2014: Earth’s energy imbalance. Journal of Climate, 27, 3129–3144, doi:10.1175/jcli-d-13-00294.1. ↩
- Waldbusser, G. G., and J. E. Salisbury, 2014: Ocean acidification in the coastal zone from an organism’s perspective: Multiple system parameters, frequency domains, and habitats. Annual Review of Marine Science, 6, 221–247, doi:10.1146/annurev-marine-121211-172238. ↩
- Wallmann, K., 2003: Feedbacks between oceanic redox states and marine productivity: A model perspective focused on benthic phosphorus cycling. Global Biogeochemical Cycles, 17, 1084, doi:10.1029/2002GB001968. ↩
- Wang, D., T. C. Gouhier, B. A. Menge, and A. R. Ganguly, 2015: Intensification and spatial homogenization of coastal upwelling under climate change. Nature, 518, 390–394, doi:10.1038/nature14235. ↩
- Wright, J. D., and M. F. Schaller, 2013: Evidence for a rapid release of carbon at the Paleocene-Eocene thermal maximum. Proceedings of the National Academy of Sciences, 110, 15908–15913, doi:10.1073/pnas.1309188110. ↩
- Yan, X.-H., T. Boyer, K. Trenberth, T. R. Karl, S.-P. Xie, V. Nieves, K.-K. Tung, and D. Roemmich, 2016: The global warming hiatus: Slowdown or redistribution? Earth’s Future, 4, 472–482, doi:10.1002/2016EF000417. ↩
- Yang, H., G. Lohmann, W. Wei, M. Dima, M. Ionita, and J. Liu, 2016: Intensification and poleward shift of subtropical western boundary currents in a warming climate. Journal of Geophysical Research Oceans, 121, 4928–4945, doi:10.1002/2015JC011513. ↩
- Zaitsev, Y. P., 1992: Recent changes in the trophic structure of the Black Sea. Fisheries Oceanography, 1, 180–189, doi:10.1111/j.1365-2419.1992.tb00036.x. ↩
- Zeebe, R. E., A. Ridgwell, and J. C. Zachos, 2016: Anthropogenic carbon release rate unprecedented during the past 66 million years. Nature Geoscience, 9, 325–329, doi:10.1038/ngeo2681. ↩
- Zickfeld, K., M. Eby, and A. J. Weaver, 2008: Carbon-cycle feedbacks of changes in the Atlantic meridional overturning circulation under future atmospheric CO2. Global Biogeochemical Cycles, 22, GB3024, doi:10.1029/2007GB003118. ↩