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Abstract As global ocean monitoring programs and marine carbon dioxide removal methods expand, so does the need for scalable biogeochemical sensors. Currently, pH sensors are widely used to measure the ocean carbonate system on a variety of autonomous platforms. This paper assesses a commercially available optical pH sensor (optode) distributed by PyroScience GmbH for oceanographic applications. Results from this study show that the small, solid‐state pH optode demonstrates a precision of 0.001 pH and relative accuracy of 0.01 pH using an improved calibration routine outlined in the manuscript. A consistent pressure coefficient of 0.029 pH/1000 dbar is observed across multiple pH optodes tested in this study. The response time is investigated for standard and fast‐response versions over a range of temperatures and flow rates. Field deployments include direct comparison to ISFET‐based pH sensor packages for both moored and profiling platforms where the pH optodes experience sensor‐specific drift rates up to 0.006 pH d⁻¹. In its current state, the pH optode potentially offers a viable and scalable option for short‐term field deployments and laboratory mesocosm studies, but not for long term deployments with no possibility for recalibration like on profiling floats. 

Increasing interest in the deployment of optical oxygen sensors, or optodes, on oceanographic moorings reflects the value of dissolved oxygen (DO) measurements in studies of physical and biogeochemical processes. Optodes are well-suited for moored applications but require careful, multi-step calibrations in the field to ensure data accuracy. Without a standardized set of protocols, this can be an obstacle for science teams lacking expertise in optode data processing and calibration. Here, we provide a set of recommendations for the deployment andin situcalibration of data from moored optodes, developed from our experience working with a set of 60 optodes deployed as part of the Gases in the Overturning and Horizontal circulation of the Subpolar North Atlantic Program (GOHSNAP). In particular, we detail the correction of drift in moored optodes, which occurs in two forms: (i) an irreversible, time-dependent drift that occurs during both optode storage and deployment and (ii) a reversible and pressure-and-time-dependent drift that is detectable in some optodes deployed at depths greater than 1,000 m. The latter is virtually unidentified in the literature yet appears to cause a low-bias in measured DO on the order of 1 to 3µmol kg⁻¹per 1,000 m of depth, appearing as an exponential decay over the first days to months of deployment. Comparisons of our calibrated DO time series against serendipitous mid-deployment conductivity-temperature-depth (CTD)-DO profiles, as well as biogeochemical (BGC)-ARGO float profiles, suggest the protocols described here yield an accuracy in optode-DO of ∼1%, or approximately 2.5 to 3µmol kg⁻¹. We intend this paper to serve as both documentation of the current best practices in the deployment of moored optodes as well as a guide for science teams seeking to collect high-quality moored oxygen data, regardless of expertise. 

Abstract. This paper provides an overview and demonstration of emerging float-based methods for quantifying gross primary production (GPP) and net community production (NCP) using Biogeochemical-Argo (BGC-Argo) float data. Recent publications have described GPP methods that are based on the detection of diurnal oscillations in upper-ocean oxygen or particulate organic carbon concentrations using single profilers or a composite of BGC-Argo floats. NCP methods rely on budget calculations to partition observed tracer variations into physical or biological processes occurring over timescales greater than 1 d. Presently, multi-year NCP time series are feasible at near-weekly resolution, using consecutive or simultaneous float deployments at local scales. Results, however, are sensitive to the choice of tracer used in the budget calculations and uncertainties in the budget parameterizations employed across different NCP approaches. Decadal, basin-wide GPP calculations are currently achievable using data compiled from the entire BGC-Argo array, but finer spatial and temporal resolution requires more float deployments to construct diurnal tracer curves. A projected, global BGC-Argo array of 1000 floats should be sufficient to attain annual GPP estimates at 10∘ latitudinal resolution if floats profile at off-integer intervals (e.g., 5.2 or 10.2 d). Addressing the current limitations of float-based methods should enable enhanced spatial and temporal coverage of marine GPP and NCP measurements, facilitating global-scale determinations of the carbon export potential, training of satellite primary production algorithms, and evaluations of biogeochemical numerical models. This paper aims to facilitate broader uptake of float GPP and NCP methods, as singular or combined tools, by the oceanographic community and to promote their continued development. 

This dataset contains discrete sample measurements of dissolved oxygen, dissolved inorganic carbon, and total alkalinity collected during cruises in 2020 (AR45) and 2022 (AR69-03) to recover and redeploy Overturning in the Subpolar North Atlantic Program (OSNAP) moorings in the Labrador Sea and western Irminger Sea. Samples in this dataset were collected as part of Gases in the Overturning and Horizontal circulation of the Subpolar North Atlantic Program (GOHSNAP), which has added moored oxygen sensors to the OSNAP mooring array, beginning in 2020. We provide the discrete sample measurements alongside salinity- and oxygen- calibrated Conductivity Temperature Depth (CTD) and oxygen sensor data from the depths where Niskin bottles were closed for sample collection. 

This dataset contains discrete sample measurements of dissolved oxygen, dissolved inorganic carbon, and total alkalinity collected during yearly Ocean Observatories Initiative (OOI) turn-around cruises to maintain the Irminger Sea Array (60.46°N, 38.44°W). Samples in this dataset were collected as part of an ancillary research project that joined the OOI turn-around cruises in June 2018 and August 2019 as part of ongoing efforts to enable OOI biogeochemical sensor data to be used to address scientific questions about ocean carbon cycling and the biological carbon pump. Discrete sample data collected and analyzed by this research team complement data collected by the OOI program as part of routine turn-around cruise activities. We provide the supplementary measurements made by our team alongside salinity- and oxygen- calibrated Conductivity Temperature Depth (CTD) and oxygen sensor data from the depths where Niskin bottles were closed for sample collection and additional discrete oxygen measurements made by the OOI team. 

Gas exchange between the atmosphere and ocean interior profoundly impacts global climate and biogeochemistry. However, our understanding of the relevant physical processes remains limited by a scarcity of direct observations. Dissolved noble gases in the deep ocean are powerful tracers of physical air-sea interaction due to their chemical and biological inertness, yet their isotope ratios have remained underexplored. Here, we present high-precision noble gas isotope and elemental ratios from the deep North Atlantic (~32°N, 64°W) to evaluate gas exchange parameterizations using an ocean circulation model. The unprecedented precision of these data reveal deep-ocean undersaturation of heavy noble gases and isotopes resulting from cooling-driven air-to-sea gas transport associated with deep convection in the northern high latitudes. Our data also imply an underappreciated and large role for bubble-mediated gas exchange in the global air-sea transfer of sparingly soluble gases, including O 2 , N 2 , and SF 6 . Using noble gases to validate the physical representation of air-sea gas exchange in a model also provides a unique opportunity to distinguish physical from biogeochemical signals. As a case study, we compare dissolved N 2 /Ar measurements in the deep North Atlantic to physics-only model predictions, revealing excess N 2 from benthic denitrification in older deep waters (below 2.9 km). These data indicate that the rate of fixed N removal in the deep Northeastern Atlantic is at least three times higher than the global deep-ocean mean, suggesting tight coupling with organic carbon export and raising potential future implications for the marine N cycle.