Explore the vast range of titles available.

Based on measurements from the WOCE/JGOFS global CO2 survey, the CLIVAR/CO2 Repeat Hydrography Program and the Canadian Line P survey, we have observed an average decrease of 0.34% yr−1 in the saturation state of surface seawater in the Pacific Ocean with respect to aragonite and calcite. The upward migrations of the aragonite and calcite saturation horizons, averaging about 1 to 2 m yr−1, are the direct result of the uptake of anthropogenic CO2 by the oceans and regional changes in circulation and biogeochemical processes. The shoaling of the saturation horizon is regionally variable, with more rapid shoaling in the South Pacific where there is a larger uptake of anthropogenic CO2. In some locations, particularly in the North Pacific Subtropical Gyre and in the California Current, the decadal changes in circulation can be the dominant factor in controlling the migration of the saturation horizon. If CO2 emissions continue as projected over the rest of this century, the resulting changes in the marine carbonate system would mean that many coral reef systems in the Pacific would no longer be able to sustain a sufficiently high rate of calcification to maintain the viability of these ecosystems as a whole, and these changes perhaps could seriously impact the thousands of marine species that depend on them for survival. Key Points The saturation state of surface waters decreased by an average of 0.34% per year The aragonite and calcite saturation horizons shoal an average of 1‐2 m per yr The shoaling of the saturation horizon is regionally variable

A successful integrated ocean acidification (OA) observing network must include 1) scientists and technicians from a range of disciplines (from physics to chemistry to biology to technology development) and across the globe; 2) government, private, and intergovernmental support; 3) regional cohorts working together on regionally specific issues; 4) publicly accessible data from the open ocean to coastal to estuarine systems; 5) close integration with other networks focusing on related measurements or issues including the social and economic consequences of OA; and 6) observation-based informational products useful for decision making such as management of fisheries and aquaculture. The Global Ocean Acidification Observing Network (GOA-ON), a key player in this vision, seeks to expand and enhance geographic extent and availability of coastal and open ocean observing data to ultimately inform adaptive measures and policy action, especially in support of the United Nations 2030 Agenda for Sustainable Development. GOA-ON works to empower and support regional collaborative networks such as the Latin American Ocean Acidification Network, supports new scientists entering the field with training, mentorship, and equipment, refines approaches for tracking biological impacts, and stimulates development of lower-cost methodology and technologies allowing for wider participation of scientists. GOA-ON seeks to collaborate with and complement work done by other observing networks such as those focused on carbon flux into the ocean, tracking of carbon and oxygen in the ocean, observing biological diversity, and determining short- and long-term variability in these and other ocean parameters through space and time.

The contribution of carbonate-producing benthic organisms to the global marine carbon budget has been overlooked, the prevailing view being that calcium carbonate (CaCO 3 ) is predominantly produced and exported by marine plankton in the \"biological pump.\" Here, we provide the first estimation of the global contribution of echinoderms to the marine inorganic and organic carbon cycle, based on organism-level measurements from species of the five echinoderm classes. Echinoderms' global CaCO 3 contribution amounts to ~0.861 Pg CaCO 3 /yr (0.102 Pg C/yr of inorganic carbon) as a production rate, and ~2.11 Pg CaCO 3 (0.25 Pg C of inorganic carbon) as a standing stock from the shelves, slopes, and abyssal depths. Echinoderm inorganic carbon production (0.102 Pg C/yr) is less than the global pelagic production (0.4-1.8 Pg C/yr) and similar to the estimates for carbonate shelves globally (0.024-0.120 Pg C/yr). Echinoderm CaCO 3 production per unit area is ~27.01 g CaCO 3 ·m −2 ·yr −1 (3.24 g C·m −2 ·yr −1 as inorganic carbon) on a global scale for all areas, with a standing stock of ~63.34 g CaCO 3 /m 2 (7.60 g C/m 2 as inorganic carbon), and ~7.97 g C/m 2 as organic carbon. The shelf production alone is 77.91 g CaCO 3 ·m −2 ·yr −1 (9.35 g C·m −2 ·yr −1 as inorganic carbon) in contrast to 2.05 g CaCO 3 ·m −2 ·yr −1 (0.24 g C·m −2 ·yr −1 as inorganic carbon) for the slope on a global scale. The biogeography of the CaCO 3 standing stocks of echinoderms showed strong latitudinal variability. More than 80% of the global CaCO 3 production from echinoderms occurs between 0 and 800 m, with the highest contribution attributed to the shelf and upper slope. We provide a global distribution of echinoderm populations in the context of global calcite saturation horizons, since undersaturated waters with respect to mineral phases are surfacing. This shallowing is a direct consequence of ocean acidification, and in some places it may reach the shelf and upper slope permanently, where the highest CaCO 3 standing stocks from echinoderms originate. These organism-level data contribute substantially to the assessment of global carbonate inventories, which at present are poorly estimated. Additionally, it is desirable to include these benthic compartments in coupled global biogeochemical models representing the \"biological pump\" and its feedbacks, since at present all efforts have focused on pelagic processes, dominated by coccolithophores. The omission of the benthic processes from modeling will only diminish the understanding of elemental fluxes at large scales and any future prediction of climate change scenarios.

Coastal and estuarine ecosystems fringing the North Pacific Ocean are particularly vulnerable to ocean acidification, hypoxia, and intense marine heatwaves as a result of interactions among natural and anthropogenic processes. Here, we characterize variability during a seasonally resolved cruise time series (2014–2018) in the southern Salish Sea (Puget Sound, Strait of Juan de Fuca) and nearby coastal waters for select physical (temperature, T; salinity, S) and biogeochemical (oxygen, O2; carbon dioxide fugacity, fCO2; aragonite saturation state, Ωarag) parameters. Medians for some parameters peaked (T, Ωarag) in surface waters in summer, whereas others (S, O2, fCO2) changed progressively across spring–fall, and all parameters changed monotonically or were relatively stable at depth. Ranges varied considerably for all parameters across basins within the study region, with stratified basins consistently the most variable. Strong environmental anomalies occurred during the time series, allowing us to also qualitatively assess how these anomalies affected seasonal patterns and interannual variability. The peak temperature anomaly associated with the 2013–2016 northeast Pacific marine heatwave–El Niño event was observed in boundary waters during the October 2014 cruise, but Puget Sound cruises revealed the largest temperature increases during the 2015–2016 timeframe. The most extreme hypoxia and acidification measurements to date were recorded in Hood Canal (which consistently had the most extreme conditions) during the same period; however, they were shifted earlier in the year relative to previous events. During autumn 2017, after the heat anomaly, a distinct carbonate system anomaly with unprecedentedly low Ωarag values and high fCO2 values occurred in parts of the southern Salish Sea that are not normally so acidified. This novel “CO2 storm” appears to have been driven by anomalously high river discharge earlier in 2017, which resulted in enhanced stratification and inferred primary productivity anomalies, indicated by persistently and anomalously high O2, low fCO2, and high chlorophyll. Unusually, this CO2 anomaly was decoupled from O2 dynamics compared with past Salish Sea hypoxia and acidification events. The complex interplay of weather, hydrological, and circulation anomalies revealed distinct multi-stressor scenarios that will potentially affect regional ecosystems under a changing climate. Further, the frequencies at which Salish cruise observations crossed known or preliminary species' sensitivity thresholds illustrates the relative risk landscape of temperature, hypoxia, and acidification anomalies in the southern Salish Sea in the present day, with implications for how multiple stressors may combine to present potential migration, survival, or physiological challenges to key regional species. The Salish cruise data product used in this publication is available at https://doi.org/10.25921/zgk5-ep63 (Alin et al., 2022), with an additional data product including all calculated CO2 system parameters available at https://doi.org/10.25921/5g29-q841 (Alin et al., 2023).

As a part of the JGOFS synthesis and modeling project, researchers have been working to synthesize the WOCE/JGOFS/DOE/NOAA global CO sub(2) survey data to better understand carbon cycling processes in the oceans. Working with international investigators we have compiled a Pacific Ocean data set with over 35,000 unique samples analyzed for at least two carbon species, oxygen, nutrients, chlorofluorocarbon (CFC) tracers, and hydrographic parameters. We use these data here to estimate in-situ oxygen utilization rates (OUR) and organic carbon remineralization rates within the upper water column of the Pacific Ocean. OURs are derived from the observed apparent oxygen utilization (AOU) and the water age estimates based on CFCs in the upper water and natural radiocarbon in deep waters. The rates are generally highest just below the euphotic zone and decrease with depth to values that are much lower and nearly constant in water deeper than 1200 m. OURs ranged from about 0.02-10 mu mol kg super(-1)yr super(-1) in the upper water masses from about 100-1000 m, and averaged = 0.10 mu mol kg super(-1)yr super(-1) in deep waters below 1200 m. The OUR data can be used to directly estimate organic carbon remineralization rates using the C:O Redfield ratio given in Anderson and Sarmiento (1994). When these rates are integrated we obtain an estimate of 5.3 plus or minus 1 Pg C yr super(-1) for the remineralization of organic carbon in the upper water column of the Pacific Ocean.

Seawater Mg:Ca and Sr:Ca ratios are biogeochemical parameters reflecting the Earth–ocean–atmosphere dynamic exchange of elements. The ratios’ dependence on the environment and organisms’ biology facilitates their application in marine sciences. Here, we present a measured single-laboratory dataset, combined with previous data, to test the assumption of limited seawater Mg:Ca and Sr:Ca variability across marine environments globally. High variability was found in open-ocean upwelling and polar regions, shelves/neritic and river-influenced areas, where seawater Mg:Ca and Sr:Ca ratios range from ∼4.40 to 6.40 mmol:mol and ∼6.95 to 9.80 mmol:mol, respectively. Open-ocean seawater Mg:Ca is semi-conservative (∼4.90 to 5.30 mol:mol), while Sr:Ca is more variable and nonconservative (∼7.70 to 8.80 mmol:mol); both ratios are nonconservative in coastal seas. Further, the Ca, Mg, and Sr elemental fluxes are connected to large total alkalinity deviations from International Association for the Physical Sciences of the Oceans (IAPSO) standard values. Because there is significant modern seawater Mg:Ca and Sr:Ca ratios variability across marine environments we cannot absolutely assume that fossil archives using taxa-specific proxies reflect true global seawater chemistry but rather taxa- and process-specific ecosystem variations, reflecting regional conditions. This variability could reconcile secular seawater Mg:Ca and Sr:Ca ratio reconstructions using different taxa and techniques by assuming an error of 1 to 1.50 mol:mol, and 1 to 1.90 mmol:mol, respectively. The modern ratios’ variability is similar to the reconstructed rise over 20 Ma (Neogene Period), nurturing the question of semi-nonconservative behavior of Ca, Mg, and Sr over modern Earth geological history with an overlooked environmental effect.

Coastal and estuarine waters of the northern California Current system and southern Salish Sea host an observational network capable of characterizing biogeochemical dynamics related to ocean acidification, hypoxia, and marine heatwaves. Here, we compiled data sets from a set of cruises conducted in estuarine waters of Puget Sound (southern Salish Sea) and its boundary waters (Strait of Juan de Fuca and Washington coast). This data product provides data from a decade of cruises with consistent formatting, extended data quality control, and multiple units for parameters such as oxygen with different end use needs and conventions. All cruises obtained high-quality temperature, salinity, inorganic carbon, nutrient, and oxygen observations to provide insight into the dynamic distribution of physical and biogeochemical conditions in this large urban estuary complex on the west coast of North America. At all sampling stations, conductivity–temperature–depth (CTD) casts included sensors for measuring temperature, conductivity, pressure, and oxygen concentrations. Laboratory analyses of discrete water samples collected at all stations throughout the water column in Niskin bottles provided measurements of dissolved inorganic carbon (DIC), dissolved oxygen, nutrient (nitrate, nitrite, ammonium, phosphate, and silicate), and total alkalinity (TA) content. This data product includes observations from 35 research cruises, including 715 oceanographic profiles, with >7490 sensor measurements of temperature, salinity, and oxygen; ≥6070 measurements of discrete oxygen and nutrient samples; and ≥4462 measurements of inorganic carbon variables (i.e., DIC and TA). The observations comprising this cruise compilation collectively characterize the spatial and temporal variability in a region with large dynamic ranges of the physical (temperature = 6.0–21.8 ∘C, salinity = 15.6–34.0) and biogeochemical (oxygen = 12–481 µmol kg−1, dissolved inorganic carbon = 1074–2362 µmol kg−1, total alkalinity = 1274–2296 µmol kg−1) parameters central to understanding ocean acidification and hypoxia in this productive estuary system with numerous interacting human impacts on its ecosystems. All observations conform to the climate-quality observing guidelines of the Global Ocean Acidification Observing Network, the US National Oceanic and Atmospheric Administration's Ocean Acidification Program, and ocean carbon community best practices. This ongoing cruise time series supports the estuarine and coastal monitoring and research objectives of the Washington Ocean Acidification Center and US National Oceanic and Atmospheric Administration (NOAA) Ocean and Atmospheric Research programs, and it provides diverse end users with the information needed to frame biological impacts research, validate numerical models, inform state and tribal water quality and fisheries management, and support decision-makers. All 2008–2018 cruise time-series measurements used in this publication are available at https://doi.org/10.25921/zgk5-ep63 (Alin et al., 2022).

The contribution of carbonate‐producing benthic organisms to the global marine carbon budget has been overlooked, the prevailing view being that calcium carbonate (CaCO 3 ) is predominantly produced and exported by marine plankton in the “biological pump.” Here, we provide the first estimation of the global contribution of echinoderms to the marine inorganic and organic carbon cycle, based on organism‐level measurements from species of the five echinoderm classes. Echinoderms' global CaCO 3 contribution amounts to ~0.861 Pg CaCO 3 /yr (0.102 Pg C/yr of inorganic carbon) as a production rate, and ~2.11 Pg CaCO 3 (0.25 Pg C of inorganic carbon) as a standing stock from the shelves, slopes, and abyssal depths. Echinoderm inorganic carbon production (0.102 Pg C/yr) is less than the global pelagic production (0.4–1.8 Pg C/yr) and similar to the estimates for carbonate shelves globally (0.024–0.120 Pg C/yr). Echinoderm CaCO 3 production per unit area is ~27.01 g CaCO 3 ·m −2 ·yr −1 (3.24 g C·m −2 ·yr −1 as inorganic carbon) on a global scale for all areas, with a standing stock of ~63.34 g CaCO 3 /m 2 (7.60 g C/m 2 as inorganic carbon), and ~7.97 g C/m 2 as organic carbon. The shelf production alone is 77.91 g CaCO 3 ·m −2 ·yr −1 (9.35 g C·m −2 ·yr −1 as inorganic carbon) in contrast to 2.05 g CaCO 3 ·m −2 ·yr −1 (0.24 g C·m −2 ·yr −1 as inorganic carbon) for the slope on a global scale. The biogeography of the CaCO 3 standing stocks of echinoderms showed strong latitudinal variability. More than 80% of the global CaCO 3 production from echinoderms occurs between 0 and 800 m, with the highest contribution attributed to the shelf and upper slope. We provide a global distribution of echinoderm populations in the context of global calcite saturation horizons, since undersaturated waters with respect to mineral phases are surfacing. This shallowing is a direct consequence of ocean acidification, and in some places it may reach the shelf and upper slope permanently, where the highest CaCO 3 standing stocks from echinoderms originate. These organism‐level data contribute substantially to the assessment of global carbonate inventories, which at present are poorly estimated. Additionally, it is desirable to include these benthic compartments in coupled global biogeochemical models representing the “biological pump” and its feedbacks, since at present all efforts have focused on pelagic processes, dominated by coccolithophores. The omission of the benthic processes from modeling will only diminish the understanding of elemental fluxes at large scales and any future prediction of climate change scenarios.

Internally consistent, quality-controlled (QC) data products play an important role in promoting regional-to-global research efforts to understand societal vulnerabilities to ocean acidification (OA). However, there are currently no such data products for the coastal ocean, where most of the OA-susceptible commercial and recreational fisheries and aquaculture industries are located. In this collaborative effort, we compiled, quality-controlled, and synthesized 2 decades of discrete measurements of inorganic carbon system parameters, oxygen, and nutrient chemistry data from the North American continental shelves to generate a data product called the Coastal Ocean Data Analysis Product in North America (CODAP-NA). There are few deep-water (> 1500 m) sampling locations in the current data product. As a result, crossover analyses, which rely on comparisons between measurements on different cruises in the stable deep ocean, could not form the basis for cruise-to-cruise adjustments. For this reason, care was taken in the selection of data sets to include in this initial release of CODAP-NA, and only data sets from laboratories with known quality assurance practices were included. New consistency checks and outlier detections were used to QC the data. Future releases of this CODAP-NA product will use this core data product as the basis for cruise-to-cruise comparisons. We worked closely with the investigators who collected and measured these data during the QC process. This version (v2021) of the CODAP-NA is comprised of 3391 oceanographic profiles from 61 research cruises covering all continental shelves of North America, from Alaska to Mexico in the west and from Canada to the Caribbean in the east. Data for 14 variables (temperature; salinity; dissolved oxygen content; dissolved inorganic carbon content; total alkalinity; pH on total scale; carbonate ion content; fugacity of carbon dioxide; and substance contents of silicate, phosphate, nitrate, nitrite, nitrate plus nitrite, and ammonium) have been subjected to extensive QC. CODAP-NA is available as a merged data product (Excel, CSV, MATLAB, and NetCDF; https://doi.org/10.25921/531n-c230, https://www.ncei.noaa.gov/data/oceans/ncei/ocads/metadata/0219960.html, last access: 15 May 2021) (Jiang et al., 2021a). The original cruise data have also been updated with data providers' consent and summarized in a table with links to NOAA's National Centers for Environmental Information (NCEI) archives (https://www.ncei.noaa.gov/access/ocean-acidification-data-stewardship-oads/synthesis/NAcruises.html).

Seawater Mg:Ca and Sr:Ca ratios are biogeochemical parameters reflecting the Earth–ocean–atmosphere dynamic exchange of elements. The ratios’ dependence on the environment and organisms’ biology facilitates their application in marine sciences. Here, we present a measured single-laboratory dataset, combined with previous data, to test the assumption of limited seawater Mg:Ca and Sr:Ca variability across marine environments globally. High variability was found in open-ocean upwelling and polar regions, shelves/neritic and river-influenced areas, where seawater Mg:Ca and Sr:Ca ratios range from ∼4.40 to 6.40 mmol:mol and ∼6.95 to 9.80 mmol:mol, respectively. Open-ocean seawater Mg:Ca is semiconservative (∼4.90 to 5.30 mol:mol), while Sr:Ca is more variable and nonconservative (∼7.70 to 8.80 mmol:mol); both ratios are nonconservative in coastal seas. Further, the Ca, Mg, and Sr elemental fluxes are connected to large total alkalinity deviations from International Association for the Physical Sciences of the Oceans (IAPSO) standard values. Because there is significant modern seawater Mg:Ca and Sr:Ca ratios variability across marine environments we cannot absolutely assume that fossil archives using taxa-specific proxies reflect true global seawater chemistry but rather taxa- and process-specific ecosystem variations, reflecting regional conditions. This variability could reconcile secular seawater Mg:Ca and Sr:Ca ratio reconstructions using different taxa and techniques by assuming an error of 1 to 1.50 mol:mol, and 1 to 1.90 mmol:mol, respectively. The modern ratios’ variability is similar to the reconstructed rise over 20 Ma (Neogene Period), nurturing the question of semi-nonconservative behavior of Ca, Mg, and Sr over modern Earth geological history with an overlooked environmental effect.