The metabolic response of thecosome pteropods from the North Atlantic and North Pacific oceans to high CO2 and low O2

© The Author(s), 2016. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Biogeosciences 13 (2016): 6191-6210, doi:10.5194/bg-13-6191-2016.As anthropogenic activities directly and indirectly increase carbon dioxide (CO2) and decrease oxygen (O2) concentrations in the ocean system, it becomes important to understand how different populations of marine animals will respond. Water that is naturally low in pH, with a high concentration of carbon dioxide (hypercapnia) and a low concentration of oxygen, occurs at shallow depths (200–500 m) in the North Pacific Ocean, whereas similar conditions are absent throughout the upper water column in the North Atlantic. This contrasting hydrography provides a natural experiment to explore whether differences in environment cause populations of cosmopolitan pelagic calcifiers, specifically the aragonitic-shelled pteropods, to have a different physiological response when exposed to hypercapnia and low O2. Using closed-chamber end-point respiration experiments, eight species of pteropods from the two ocean basins were exposed to high CO2 ( ∼  800 µatm) while six species were also exposed to moderately low O2 (48 % saturated, or  ∼  130 µmol kg−1) and a combined treatment of low O2/high CO2. None of the species tested showed a change in metabolic rate in response to high CO2 alone. Of those species tested for an effect of O2, only Limacina retroversa from the Atlantic showed a response to the combined treatment, resulting in a reduction in metabolic rate. Our results suggest that pteropods have mechanisms for coping with short-term CO2 exposure and that there can be interactive effects between stressors on the physiology of these open ocean organisms that correlate with natural exposure to low O2 and high CO2. These are considerations that should be taken into account in projections of organismal sensitivity to future ocean conditions.This work was funded by the National Science Foundation’s Ocean Acidification Program (grant OCE-1041068), the National Institute of Standards and Technology (NIST-60NANB10D024), and the WHOI postdoctoral scholarship program

Accelerating global ocean observing: monitoring the coastal ocean through broadly accessible, low-cost sensor networks

© The Author(s), 2021. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Wang, Z. A., Michel, A. P. M., & Mooney, T. A. Accelerating global ocean observing: monitoring the coastal ocean through broadly accessible, low-cost sensor networks. Marine Technology Society Journal, 55(3), (2021): 82–83, https://doi.org/10.4031/MTSJ.55.3.52.The global coastal ocean provides food and other critical resources to human societies. Yet this habitat, for which many depend, has experienced severe degradation from human activities. The rates of human-induced changes along the coast demand significantly improved coverage of ocean observations in order to support science-based decision making and policy formation tailored to specific regions. Our proposal envisions developing a global network of low-cost, easily produced and readily deployed oceanographic sensors for use on a wide variety of platforms in the coastal ocean. A substantially large number of these sensors can thus be installed on existing infrastructure, ships of opportunity, and fishing fleets, or even individually along the coast, particularly in vulnerable and disadvantaged regions. This would vastly increase the spatiotemporal resolution of the current data coverage along the coast, allowing greater equitable access. It would also offer significant opportunities for partnership with communities, NGOs, governments, and other stakeholders, as well as a wide range of commercial and industrial sectors to develop and deploy sensors in scalable networks transmitting data in near-real time. Finally, it presents a vastly lowered bar for participation by citizen scientists and other engaged members of the public to address location-specific coastal problems anywhere in the world.National Science Foundation; Project Title “Collaborative Research: IDBR: Type A: A High-resolution bio-sensor to simultaneously measure the behavior, vital rates and environment of key marine organisms”; Award Number 1455593 to ZAW and TAM

Seasonal controls of aragonite saturation states in the Gulf of Maine

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 Journal of Geophysical Research: Oceans 122 (2017): 372–389, doi:10.1002/2016JC012373.The Gulf of Maine (GoME) is a shelf region especially vulnerable to ocean acidification (OA) due to natural conditions of low pH and aragonite saturation states (Ω-Ar). This study is the first to assess the major oceanic processes controlling seasonal variability of the carbonate system and its linkages with pteropod abundance in Wilkinson Basin in the GoME. Two years of seasonal sampling cruises suggest that water-column carbonate chemistry in the region undergoes a seasonal cycle, wherein the annual cycle of stratification-overturn, primary production, respiration-remineralization and mixing all play important roles, at distinct spatiotemporal scales. Surface production was tightly coupled with remineralization in the benthic nepheloid layer during high production seasons, which results in occasional aragonite undersaturation. From spring to summer, carbonate chemistry in the surface across Wilkinson Basin reflects a transition from a production-respiration balanced system to a net autotropic system. Mean water-column Ω-Ar and abundance of large thecosomatous pteropods show some correlation, although patchiness and discrete cohort reproductive success likely also influence their abundance. Overall, photosynthesis-respiration is the primary driving force controlling Ω-Ar variability during the spring-to-summer transition as well as over the seasonal cycle. However, calcium carbonate (CaCO3) dissolution appears to occur near bottom in fall and winter when bottom water Ω-Ar is generally low but slightly above 1. This is accompanied by a decrease in pteropod abundance that is consistent with previous CaCO3 flux trap measurements. The region might experience persistent subsurface aragonite undersaturation in 30–40 years under continued ocean acidification.Coastal Ocean Institute at Woods Hole Oceanographic Institution; National Science Foundation Grant Number: (OCE-1316040)2017-07-2

The effect of elevated carbon dioxide on the sinking and swimming of the shelled pteropod Limacina retroversa

Author Posting. © The Author(s), 2017. This is the author's version of the work. It is posted here under a nonexclusive, irrevocable, paid-up, worldwide license granted to WHOI. It is made available for personal use, not for redistribution. The definitive version was published in ICES Journal of Marine Science 74 (2017): 1893–1905, doi:10.1093/icesjms/fsx008.Shelled pteropods are planktonic molluscs that may be affected by ocean acidification. Limacina retroversa from the Gulf of Maine were used to investigate the impact of elevated carbon dioxide (CO2) on shell condition as well as swimming and sinking behaviours. Limacina retroversa were maintained at either ambient (ca. 400 μatm) or two levels of elevated CO2 (800 and 1200 μatm) for up to four weeks, and then examined for changes in shell transparency, sinking speed, and swimming behaviour assessed through a variety of metrics (e.g., speed, path tortuosity, wing beat frequency). After exposures to elevated CO2 for as little as four days, the pteropod shells were significantly darker and more opaque in the elevated CO2 treatments. Sinking speeds were significantly slower for pteropods exposed to medium and high CO2 in comparison to the ambient treatment. Swimming behaviour showed less clear patterns of response to treatment and duration of exposure, but overall, swimming did not appear to be hindered under elevated CO2. Sinking is used by L. retroversa for predator evasion, and altered speeds and increased visibility could increase the susceptibility of pteropods to predation.Funding for this research was provided by a National Science Foundation grant to Lawson, Maas, and Tarrant (OCE-1316040). Additional support for field sampling was provided by the WHOI Coastal Ocean Institute, Pickman Foundation, and the Tom Haas Fund at the New Hampshire Charitable Foundation

Deciphering the dynamics of inorganic carbon export from intertidal salt marshes using high-frequency measurements

© The Author(s), 2018. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Marine Chemistry 206 (2018): 7-18, doi:10.1016/j.marchem.2018.08.005.The lateral export of carbon from coastal marshes via tidal exchange is a key component of the marsh carbon budget and coastal carbon cycles. However, the magnitude of this export has been difficult to accurately quantify due to complex tidal dynamics and seasonal cycling of carbon. In this study, we use in situ, high-frequency measurements of dissolved inorganic carbon (DIC) and water fluxes to estimate lateral DIC fluxes from a U.S. northeastern salt marsh. DIC was measured by a CHANnelized Optical Sensor (CHANOS) that provided an in situ concentration measurement at 15-min intervals, during periods in summer (July – August) and late fall (December). Seasonal changes in the marsh had strong effects on DIC concentrations, while tidally-driven water fluxes were the fundamental vehicle of marsh carbon export. Episodic events, such as groundwater discharge and mean sea water level changes, can impact DIC flux through altered DIC concentrations and water flow. Variability between individual tides within each season was comparable to mean variability between the two seasons. Estimated mean DIC fluxes based on a multiple linear regression (MLR) model of DIC concentrations and high-frequency water fluxes agreed reasonably well with those derived from CHANOS DIC measurements for both study periods, indicating that high-frequency, modeled DIC concentrations, coupled with continuous water flux measurements and a hydrodynamic model, provide a robust estimate of DIC flux. Additionally, an analysis of sampling strategies revealed that DIC fluxes calculated using conventional sampling frequencies (hourly to two-hourly) of a single tidal cycle are unlikely to capture a representative mean DIC flux compared to longer-term measurements across multiple tidal cycles with sampling frequency on the order of tens of minutes. This results from a disproportionately large amount of the net DIC flux occurring over a small number of tidal cycles, while most tides have a near-zero DIC export. Thus, high-frequency measurements (on the order of tens of minutes or better) over the time period of interest are necessary to accurately quantify tidal exports of carbon species from salt marshes.This work was funded by NSF Graduate Research Fellowship Program, NSF Ocean Sciences Postdoctoral Fellowship (OCE-1323728), Link FoundationOcean Engineering and Instrumentation Fellowship, National Institute of Science and Technology (NIST no. 60NANB10D024), the USGS LandCarbon and Coastal & Marine Geology Programs, NSF Chemical Oceanography Program (OCE-1459521), NSF Ocean Technology and Interdisciplinary Coordination program (OCE-1233654) and NOAA Science Collaborative (NA09NOS4190153)

Intertidal salt marshes as an important source of inorganic carbon to the coastal ocean

© The Author(s), 2016. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Limnology and Oceanography 61 (2016): 1916–1931, doi:10.1002/lno.10347.Dynamic tidal export of dissolved inorganic carbon (DIC) to the coastal ocean from highly productive intertidal marshes and its effects on seawater carbonate chemistry are thoroughly evaluated. The study uses a comprehensive approach by combining tidal water sampling of CO2 parameters across seasons, continuous in situ measurements of biogeochemically-relevant parameters and water fluxes, with high-resolution modeling in an intertidal salt marsh of the U.S. northeast region. Salt marshes can acidify and alkalize tidal water by injecting CO2 (DIC) and total alkalinity (TA). DIC and TA generation may also be decoupled due to differential effects of marsh aerobic and anaerobic respiration on DIC and TA. As marsh DIC is added to tidal water, the buffering capacity first decreases to a minimum and then increases quickly. Large additions of marsh DIC can result in higher buffering capacity in ebbing tide than incoming tide. Alkalization of tidal water, which mostly occurs in the summer due to anaerobic respiration, can further modify buffering capacity. Marsh exports of DIC and alkalinity may have complex implications for the future, more acidified ocean. Marsh DIC export exhibits high variability over tidal and seasonal cycles, which is modulated by both marsh DIC generation and by water fluxes. The marsh DIC export of 414 g C m−2 yr−1, based on high-resolution measurements and modeling, is more than twice the previous estimates. It is a major term in the marsh carbon budget and translates to one of the largest carbon fluxes along the U.S. East Coast.USGS Coastal & Marine Geology Program; U.S. National Science Foundation Grant Number: OCE-1459521; NOAA Science Collaborative Grant Number: NA09NOS4190153; USGS LandCarbon Progra

Changes in anthropogenic carbon storage in the Northeast Pacific in the last decade

Author Posting. © American Geophysical Union, 2016. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research: Oceans 121 (2016): 4618–4632, doi:10.1002/2016JC011775.In order to understand the ocean's role as a sink for anthropogenic carbon dioxide (CO2), it is important to quantify changes in the amount of anthropogenic CO2 stored in the ocean interior over time. From August to September 2012, an ocean acidification cruise was conducted along a portion of the P17N transect (50°N 150°W to 33.5°N 135°W) in the Northeast Pacific. These measurements are compared with data from the previous occupation of this transect in 2001 to estimate the change in the anthropogenic CO2 inventory in the Northeast Pacific using an extended multiple linear regression (eMLR) approach. Maximum increases in the surface waters were 11 µmol kg−1 over 11 years near 50°N. Here, the penetration depth of anthropogenic CO2 only reached ∼300 m depth, whereas at 33.5°N, penetration depth reached ∼600 m. The average increase of the depth-integrated anthropogenic carbon inventory was 0.41 ± 0.12 mol m−2 yr−1 across the transect. Lower values down to 0.20 mol m−2 yr−1 were observed in the northern part of the transect near 50°N and increased up to 0.55 mol m−2 yr−1 toward 33.5°N. This increase in anthropogenic carbon in the upper ocean resulted in an average pH decrease of 0.002 ± 0.0003 pH units yr−1 and a 1.8 ± 0.4 m yr−1 shoaling rate of the aragonite saturation horizon. An average increase in apparent oxygen utilization of 13.4 ± 15.5 µmol kg−1 centered on isopycnal surface 26.6 kg m−3 from 2001 to 2012 was also observed.National Science Foundation Ocean Acidification Program Grant Number: OCE-1041068; National Institute of Standards and Technology Grant Number: (NIST-60NANB10D024); National Science Foundation Graduate Research Fellowship Program2017-01-0

Effects of typhoons on surface seawater pCO(2) and air-sea CO2 fluxes in the Northern South China Sea

Author Posting. © American Geophysical Union, 2020. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research: Oceans 125(8), (2020): e2020JC016258, doi:10.1029/2020JC016258.This study assessed the effects of typhoons on sea surface pCO2 and CO2 flux in the northern South China Sea (SCS). During the passage of three major typhoons from May to August 2013, sea surface pCO2, surface seawater temperature (SST), and other meteorological parameters were continuously measured on a moored buoy. Surface water in the region was a source of CO2 to the atmosphere with large variations ranging from hours to months. SST was the primary factor controlling the variation of surface pCO2 through most of the time period. Typhoons are seen to impact surface pCO2 in three steps: first by cooling, thus decreasing surface pCO2, and then by causing vertical mixing that brings up deep, high‐CO2 water, and lastly triggering net uptake of CO2 due to the nutrients brought up in this deep water. The typhoons of this study primarily impacted air‐sea CO2 flux via increasing wind speeds. The mean CO2 flux during a typhoon ranged from 3.6 to 5.4 times the pretyphoon mean flux. The magnitude of the CO2 flux during typhoons was strongly inversely correlated with the typhoon center distance. The effect of typhoons accounted for 22% of the total CO2 flux in the study period, during which typhoons occurred only 9% of the time. It was estimated that typhoons enhanced annual CO2 efflux by 23–56% in the northern SCS during the last decade. As such, tropical cyclones may play a large and increasingly important role in controlling CO2 fluxes in a warmer and stormier ocean of the future.This study was supported by the Marine Public Welfare Project of China (Grant 200905012), the Scientific Research Fund of the Second Institute of Oceanography of China (Grant JT1502), the Global Change and Air‐Sea Interaction project of China (Grant GASI‐03‐01‐02‐02), and the National Natural Sciences Foundation of China (Grant 91128212).2021-02-0

Particle triggered reactions as an important mechanism of alkalinity and inorganic carbon removal in river plumes

Author Posting. © American Geophysical Union, 2021. 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 48(11), (2021): e2021GL093178, https://doi.org/10.1029/2021GL093178.The effects of heterogeneous reactions between river-borne particles and the carbonate system were studied in the plumes of the Mississippi and Brazos rivers. Measurements within these plumes revealed significant removal of dissolved inorganic carbon (DIC) and total alkalinity (TA). After accounting for all known DIC and TA sinks and sources, heterogeneous reactions (i.e., heterogeneous CaCO3 precipitation and cation exchange between adsorbed and dissolved ions) were found to be responsible for a significant fraction of DIC and TA removal, exceeding 10% and 90%, respectively, in the Mississippi and Brazos plume waters. This finding was corroborated by laboratory experiments, in which the seeding of seawater with the riverine particles induced the removal of the DIC and TA. The combined results demonstrate that heterogeneous reactions may represent an important controlling mechanism of the seawater carbonate system in particle-rich coastal areas and may significantly impact the coastal carbon cycle.This research was funded by the National Science Foundation (NSF) and the Bi-National Science Foundation U.S-Israel award number OCE-BSF 1635388.2021-11-2