Coastal Ocean Acidification Along the Washington Coast Adjacent to the Salish Sea

The continental shelf waters off the west coast of North America are exposed to water with increasing concentrations of anthropogenic CO2 (Canthro) from exchanges with the atmosphere and the shoreward transport and mixing of upwelled water from the south and west. Hydrographic measurements were made offshore of the west coast of the United States and Canada on the RV Ronald H. Brown on the West Coast Ocean Acidification cruise in June and July of 2021 (WCOA2021). The primary goal of this WCOA2021 cruise was to measure the physics, chemistry, and biology of this region from Queen Charlotte Sound in British Columbia to southern California in order to develop a clearer understanding of the intersection of natural and anthropogenic ocean acidification, deoxygenation, and biogeochemical cycling processes in these waters. This region is a natural laboratory for studying the chemical and ecological impacts of ocean acidification and deoxygenation due to spring and summertime wind-driven upwelling of cold waters that are rich in re-mineralized carbon and nutrients and poor in oxygen. The upwelled nutrients drive intense cycling of organic matter that is created through photosynthesis in the surface ocean and degraded through biological respiration in subsurface habitats. We observed reductions in pH and decreases in aragonite saturation state of up to 0.1 and 0.2, respectively, relative to a linear mixing model for surface and subsurface waters due to the enhanced respiration processes in the subsurface waters off the coasts of Washington and Oregon where hypoxic conditions prevailed over much of the region. These conditions for dissolved oxygen, pH and aragonite saturation state in the subsurface waters were below critical thresholds for several marine species of importance to the California Current Ecosystem

Dissolution dominating calcification process in polar pteropods close to the point of aragonite undersaturation

Thecosome pteropods are abundant upper-ocean zooplankton that build aragonite shells. Ocean acidification results in the lowering of aragonite saturation levels in the surface layers, and several incubation studies have shown that rates of calcification in these organisms decrease as a result. This study provides a weight-specific net calcification rate function for thecosome pteropods that includes both rates of dissolution and calcification over a range of plausible future aragonite saturation states (Omega_Ar). We measured gross dissolution in the pteropod Limacina helicina antarctica in the Scotia Sea (Southern Ocean) by incubating living specimens across a range of aragonite saturation states for a maximum of 14 days. Specimens started dissolving almost immediately upon exposure to undersaturated conditions (Omega_Ar,0.8), losing 1.4% of shell mass per day. The observed rate of gross dissolution was different from that predicted by rate law kinetics of aragonite dissolution, in being higher at Var levels slightly above 1 and lower at Omega_Ar levels of between 1 and 0.8. This indicates that shell mass is affected by even transitional levels of saturation, but there is, nevertheless, some partial means of protection for shells when in undersaturated conditions. A function for gross dissolution against Var derived from the present observations was compared to a function for gross calcification derived by a different study, and showed that dissolution became the dominating process even at Omega_Ar levels close to 1, with net shell growth ceasing at an Omega_Ar of 1.03. Gross dissolution increasingly dominated net change in shell mass as saturation levels decreased below 1. As well as influencing their viability, such dissolution of pteropod shells in the surface layers will result in slower sinking velocities and decreased carbon and carbonate fluxes to the deep ocean

Ocean Acidification: The Other CO\u3csub\u3e2\u3c/sub\u3e Problem?

Rising atmospheric carbon dioxide (CO2), primarily from human fossil fuel combustion, reduces ocean pH and causes wholesale shifts in seawater carbonate chemistry. The process of ocean acidification is well documented in field data, and the rate will accelerate over this century unless future CO2 emissions are curbed dramatically. Acidification alters seawater chemical speciation and biogeochemical cycles of many elements and compounds. One well-known effect is the lowering of calcium carbonate saturation states, which impacts shell-forming marine organisms from plankton to benthic molluscs, echinoderms, and corals. Many calcifying species exhibit reduced calcification and growth rates in laboratory experiments under high-CO2 conditions. Ocean acidification also causes an increase in carbon fixation rates in some photosynthetic organisms (both calcifying and noncalcifying). The potential for marine organisms to adapt to increasing CO2 and broader implications for ocean ecosystems are not well known; both are high priorities for future research. Although ocean pH has varied in the geological past, paleo-events may be only imperfect analogs to current conditions. Republished with permission from 1 Ann. Rev. Mar. Sci. 169 (2009)

Distribution of Hydrocarbons and Microbial Populations Related to Sedimentation Processes in Lower Cook Inlet and Norton Sound, Alaska

In spring and summer 1978 and spring 1979 an integrated study was carried out to examine the interrelationships of physical (sediment deposition), chemical (organic carbon and hydrocarbon concentrations), and biological (microbial populations and activities) factors in the Cook Inlet and Norton Sound regions with respect to the probable sinks and fates of hydrocarbon contaminants within these ecosystems. Most of the fine-grained sediment entering Cook Inlet is transported out of the inlet into Shelikof Strait. However, significant sediment accumulation occurs within areas of Kamishak and Kachemak bays. In Norton Sound, sediment from the Yukon River is transported counterclockwise around the embayment and approximately 50% is deposited in the nearshore regions of the sound. In both regions, areas of high sediment accumulation are richer in organic carbon and hydrocarbon derived from land than are areas of low sediment accumulation. In general, areas with high sediment accumulation rates for fine-grained particles are also areas of relatively high microbial activity. Results suggest that these elevated microbial activities reflect biodegradation of detrital carbon associated with these particles. Also, the Cook Inlet and Norton Sound region were found to be free from petroleum hydrocarbon contamination (with the exception of one area in Cook Inlet). No evidence was found of hydrocarbon accumulation resulting from a gas seepage in Norton Sound, nor for accumulation of hydrocarbons in sediments of lower Cook Inlet and Shelikof Strait from oil well operations in upper Cook Inlet.Key words: arctic marine ecosystems, sedimentation, microorganism, hydrocarbons, lower Cook Inlet, Norton SoundMots clés: écosystèmes marins arctiques, sédimentation, micro-organismes, hydrocarbons, sud de l'inlet Cook, bras de mer Norto

Quantifying the Flux of Caco3 and Organic Carbon from the Surface Ocean Using in Situ Measurements of O-2, N-2, Pco(2), and Ph

Ocean acidification from anthropogenic CO2 has focused our attention on the importance of understanding the rates and mechanisms of CaCO3 formation so that changes can be monitored and feedbacks predicted. We present a method for determining the rate of CaCO3 production using in situ measureme nts of fCO(2) and pH in surface waters of the eastern subarctic Pacific Ocean. These quantities were determined on a surface mooring every 3 h for a period of about 9 months in 2007 at Ocean Station Papa (50 degrees N, 145 degrees W). We use the data in a simple surface ocean, mass balance model of dissolved inorganic carbon (DIC) and alkalinity (Alk) to constrain the CaCO3: organic carbon (OC) production ratio to be approximately 0.5. A CaCO3 production rate of 8 mmol CaCO3 m(-2) d(-1) in the summer of 2007 (1.2 mol m(-2) yr(-1)) is derived by combining the CaCO3: OC ratio with the a net organic carbon production rate (2.5 mol C m(-2) yr(-1)) determined from in situ measurements of oxygen and nitrogen gas concentrations measured on the same mooring (Emerson and Stump, 2010). Carbonate chemistry data from a meridional hydrographic section in this area in 2008 indicate that isopycnal surfaces that outcrop in the winter in the subarctic Pacific and deepen southward into the subtropics are a much stronger source for alkalinity than vertical mixing. This pathway has a high enough Alk: DIC ratio to support the CaCO3: OC production rate implied by the fCO(2) and pH data

Variability and trends in surface seawater pCO2 and CO2 flux in the Pacific Ocean

Author Posting. © American Geophysical Union, 2017. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 44 (2017): 5627–5636, doi:10.1002/2017GL073814.Variability and change in the ocean sink of anthropogenic carbon dioxide (CO2) have implications for future climate and ocean acidification. Measurements of surface seawater CO2 partial pressure (pCO2) and wind speed from moored platforms are used to calculate high-resolution CO2 flux time series. Here we use the moored CO2 fluxes to examine variability and its drivers over a range of time scales at four locations in the Pacific Ocean. There are significant surface seawater pCO2, salinity, and wind speed trends in the North Pacific subtropical gyre, especially during winter and spring, which reduce CO2 uptake over the 10 year record of this study. Starting in late 2013, elevated seawater pCO2 values driven by warm anomalies cause this region to be a net annual CO2 source for the first time in the observational record, demonstrating how climate forcing can influence the timing of an ocean region shift from CO2 sink to source.NOAA, OAR, CPO, OOMD Grant Number: 100007298; NOAA, OAR, CPO, OOMD Grant Number: NA09OAR4320129; Ocean Observation and Monitoring Division (OOMD) Grant Number: NA09OAR4320129; National Oceanic and Atmospheric Administration (NOAA) Grant Number: 1000072982017-12-1

Satellite-based prediction of pCO2 in coastal waters of the eastern North Pacific

Continental margin carbon cycling is complex, highly variable over a range of space and time scales, and forced by multiple physical and biogeochemical drivers. Predictions of globally significant air–sea CO2 fluxes in these regions have been extrapolated based on very sparse data sets. We present here a method for predicting coastal surface-water pCO2 from remote-sensing data, based on self organizing maps (SOMs) and a nonlinear semi-empirical model of surface water carbonate chemistry. The model used simple empirical relationships between carbonate chemistry (total dissolved carbon dioxide (TCO2) and alkalinity (TAlk)) and satellite data (sea surface temperature (SST) and chlorophyll (Chl)). Surface-water CO2 partial pressure (pCO2) was calculated from the empirically-predicted TCO2 and TAlk. This directly incorporated the inherent nonlinearities of the carbonate system, in a completely mechanistic manner. The model’s empirical coefficients were determined for a target study area of the central North American Pacific continental margin (22–50°N, within 370 km of the coastline), by optimally reproducing a set of historical observations paired with satellite data. The model-predicted pCO2 agreed with the highly variable observations with a root mean squared (RMS) deviation of 0.8 (r = 0.81; r2 = 0.66). This level of accuracy is a significant improvement relative to that of simpler models that did not resolve the biogeochemical sub-regions or that relied on linear dependences on input parameters. Air–sea fluxes based on these pCO2 predictions and satellite-based wind speed measurements suggest that the region is a ∼14 Tg C yr−1 sink for atmospheric CO2 over the 1997–2005 period, with an approximately equivalent uncertainty, compared with a ∼0.5 Tg C yr−1 source predicted by a recent bin-averaging and interpolation-based estimate for the same area.Fil: Hales, Burke. State University of Oregon; Estados UnidosFil: Strutton, Peter G.. University Of Tasmania; AustraliaFil: Saraceno, Martin. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones del Mar y la Atmosfera. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Centro de Investigaciones del Mar y la Atmosfera; ArgentinaFil: Letelier, Ricardo. State University of Oregon; Estados UnidosFil: Takahashi, Taro. Lamont-Doherty Earth Observatory; Estados UnidosFil: Feely, Richard. National Oceanic and Atmospheric Administration. Pacific Marine Environmental Laboratory; Estados UnidosFil: Sabine, Christopher. National Oceanic and Atmospheric Administration. Pacific Marine Environmental Laboratory; Estados UnidosFil: Chavez, Francisco. Monterey Bay Aquarium Research Institute; Estados Unido

The regulation of equatorial Pacific new production and pCO 2 by silicate-limited diatoms

a b s t r a c t Modeling and data from the JGOFS EqPac program suggested that the eastern equatorial Pacific upwelling ecosystem includes a quasi-chemostat culture system dominated by diatoms and limited by Si(OH) 4 due to a low ratio of Si(OH) 4 to NO 3 in the upwelling source water, the Equatorial Undercurrent. Diatoms were hypothesized to be the major users of NO 3 in this system and the amount assimilated limited by the low amount of Si(OH) 4 available. As a consequence NO 3 is left in the surface waters along with unused CO 2 . Two cruises to the eastern equatorial Pacific (EB04 and EB05) were made to test the existing hypothesis of Si(OH) 4 limitation, and study the roles of source concentrations of Si(OH) 4 and Fe, and nutrient uptake kinetics for comparison with model predictions. Fractionated nitrogen uptake measurements showed that diatoms at times take up the major portion of the NO 3 . Picoplankton and some phytoplankton in the 4 5-mm size group carried out primarily regenerated production, i.e. NH 4 uptake in a grazing dominated system. Equatorial diatoms followed uptake kinetics for Si(OH) 4 and NO 3 uptake as observed in laboratory investigations of diatoms under Si(OH) 4 and Fe limitations. Si(OH) 4 uptake responded to additions of Si(OH) 4 on a time scale of hours in uptake kinetic experiments while NO 3 uptake was unaffected by added NO 3 . The uptake of Si(OH) 4 varied in a narrow range on a Michaelis-Menten hyperbola of Si(OH) 4 uptake vs. Si(OH) 4 concentration, with a maximal Si(OH) 4 uptake rate, V 0 maxSi set to a relatively low value by some factor(s) other than Fe on a longer time scale, i.e., days in shipboard enclosures. Simply enclosing water collected from the mid euphotic zone and incubating for some days on deck at 50% surface irradiance increased

Comparison of CO2 dynamics and air-sea exchange in differing tropical reef environments

Author Posting. © The Author(s), 2013. This is the author's version of the work. It is posted here by permission of Springer for personal use, not for redistribution. The definitive version was published in Aquatic Geochemistry 19 (2013): 371-397, doi:10.1007/s10498-013-9214-7.Note from corresponding author: authors Feely and Shamberger were added after the initial submission, but before the final submission.An array of MAPCO2 buoys, CRIMP-2, Ala Wai, and Kilo Nalu, deployed in the coastal waters of Hawaii have produced multiyear high temporal resolution CO2 records in three different coral reef environments off the island of Oahu, Hawaii. This study, which includes data from June 2008-December 2011, is part of an integrated effort to understand the factors that influence the dynamics of CO2-carbonic acid system parameters in waters surrounding Pacific high island coral reef ecosystems and subject to differing natural and anthropogenic stresses. The MAPCO2 buoys are located on the Kaneohe Bay backreef, and fringing reef sites on the south shore of O’ahu, Hawai’i. The buoys measure CO2 and O2 in seawater and in the atmosphere at 3-hour intervals, as well as other physical and biogeochemical parameters (CTD, chlorophyll-a, turbidity). The buoy records, combined with data from synoptic spatial sampling, have allowed us to examine the interplay between biological cycles of productivity/respiration and calcification/dissolution and biogeochemical and physical forcings on hourly to inter-annual time scales. Air-sea CO2 gas exchange was also calculated to determine if the locations were sources or sinks of CO2 over seasonal, annual, and interannual time periods. Net annualized fluxes for CRIMP-2, Ala Wai, and Kilo Nalu over the entire study period were 1.15 mol C m-2 yr-1, 0.045 mol C m-2 yr-1, and -0.0056 mol C m-2 yr-1, respectively, where positive values indicate a source or a CO2 flux from the water to the atmosphere, and negative values indicate a sink or flux of CO2 from the atmosphere into the water. These values are of similar magnitude to previous estimates in Kaneohe Bay as well as those reported from other tropical reef environments. Total alkalinity (AT) was measured in conjunction with pCO2 and the carbonic acid system was calculated to compare with other reef systems and open ocean values around Hawaii. These findings emphasize the need for high-resolution data of multiple parameters when attempting to characterize the carbonic-acid system in locations of highly variable physical, chemical, and biological parameters (e.g. coastal systems, reefs).This work was supported in part by a grant/cooperative agreement from the National Oceanic and Atmospheric Administration, Project R/IR-3, which is sponsored by the University of Hawaii Sea Grant College Program, SOEST, under Institutional Grant No. NA09OAR4170060 from NOAA Office of Sea Grant, Department of Commerce.2014-11-0