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Archive for New OCB Research – Page 11

Sea ice loss amplifies CO2 increase in the Arctic

Posted by mmaheigan 
· Thursday, January 7th, 2021 

Warming and sea ice loss over the past few decades have caused major changes in sea surface partial pressure of CO2 (pCO2) of the western Arctic Ocean, but detailed temporal variations and trends during this period of rapid climate-driven changes are not well known.

Based on an analysis of an international Arctic pCO2 synthesis data set collected between 1994-2017, the authors of a recent paper published in Nature Climate Change observed that summer sea surface pCO2 in the Canada Basin is increasing at twice the rate of atmospheric CO2 rise. Warming, ice loss and subsequent CO2 uptake in the Basin are amplifying seasonal pCO2 changes, resulting in a rapid long-term increase. Consequently, the summer air-sea CO2 gradient has decreased sharply and may approach zero by the 2030s, which is reducing the basin’s capacity to remove CO2 from the atmosphere. In stark contrast, sea surface pCO2 on the Chukchi Shelf remains low and relatively constant during this time frame, which the authors attribute to increasingly strong biological production in response to higher intrusion of nutrient-rich Pacific Ocean water onto the shelf as a result of increased Bering Strait throughflow. These trends suggest that, unlike the Canada Basin, the Chukchi Shelf will become a larger carbon sink in the future, with implications for the deep ocean carbon cycle and ecosystem.

As Arctic sea ice melting accelerates, more fresh, low-buffer capacity, high-CO2 water will enter the upper layer of the Canada Basin, which may rapidly acidify the surface water, endanger marine calcifying organisms, and disrupt ecosystem function.

Figure. 1: TOP) Sea surface pCO2 trend in the Canada Basin and Chukchi Shelf. The grey dots represent the raw observations of pCO2, black dots are the monthly mean of pCO2 at in situ SST, and red dots are the monthly means of pCO2 normalized to the long-term means of SST. The arrows indicate the statistically significant change in ∆pCO2. BOTTOM) Sea ice-loss amplifying surface water pCO2 in the Canada Basin. Black dots represent the initial condition for pCO2 and DIC at -1.6 ℃. The arrows indicate the processes of warming (red), CO2 uptake from the atmosphere (green), dilution by ice meltwater (blue). The yellow shaded areas indicate the possible seasonal variations of pCO2, which are amplified by the synergistic effect of ice melt, warming and CO2 uptake.

Authors:
Zhangxian Ouyang (University of Delaware, USA),
Di Qi (Third Institute of Oceanography, China),
Liqi Chen (Third Institute of Oceanography, China),
Taro Takahashi† (Columbia University, USA),
Wenli Zhong (Ocean University of China, China),
Michael D. DeGrandpre (University of Montana, USA),
Baoshan Chen (University of Delaware, USA),
Zhongyong Gao (Third Institute of Oceanography, China),
Shigeto Nishino (Japan Agency for Marine-Earth Science and Technology, Japan),
Akihiko Murata (Japan Agency for Marine-Earth Science and Technology, Japan),
Heng Sun (Third Institute of Oceanography, China),
Lisa L. Robbins (University of South Florida, USA),
Meibing Jin (International Arctic Research Center, USA),
Wei-Jun Cai* (University of Delaware, USA)

Ice sheets mobilize trace elements for export downstream

Posted by mmaheigan 
· Thursday, January 7th, 2021 

Trace elements are essential micronutrients for life in the ocean and also serve as valuable fingerprints of chemical weathering. The behaviour of trace elements in the ocean has gained interest because some of these elements are found at vanishingly low concentrations that limit ecosystem productivity. Despite delivering >2000 km3 yr-1 of freshwater to the polar oceans, ice sheets have largely been overlooked as major trace element sources. This is partly due to a lack of data on meltwater endmember chemistry beneath and emerging from the Greenland and Antarctic ice sheets, which cover 10% of Earth’s land surface area, and partly because meltwaters were previously assumed to be dilute compared to most river waters.

In a study published in PNAS, authors analysed the trace element composition of meltwaters from the Mercer Subglacial Lake, a hydrologically active subglacial lake >1000 m below the surface of the Antarctic Ice Sheet, and a meltwater river emerging from beneath a large outlet glacier of the Greenland Ice Sheet (Leverett Glacier). These subglacial meltwaters (i.e., water travelling along the ice-rock interface beneath an ice mass) contained much higher concentrations of trace elements than anticipated. For example, typically immobile elements like iron and aluminium were observed in the dissolved phase (<0.45 µm) at much higher concentrations than in mean river or open ocean waters (up to 20,900 nM for Fe and 69,100 nM for Al), but exhibited large size fractionation between colloidal/nanoparticulate (0.02 – 0.45 µm) and soluble (<0.02 µm) size fractions (Figure 1). Subglacial physical and biogeochemical weathering processes are thought to mobilize many of these trace elements from the bedrock and sediments beneath ice sheets and export them downstream. Antarctic subglacial meltwaters were more enriched in dissolved trace elements than Greenland Ice Sheet outflow, which is likely due to longer subglacial residence times, lack of dilution from surface meltwater inputs, and differences in underlying sediment geology.

These results indicate that ice sheet systems can mobilize large quantities of trace elements from the land to the ocean and serve as major contributors to regional elemental cycles (e.g., coastal Southern Ocean). In a warming climate with increasing ice sheet runoff, subglacial meltwaters will become an increasingly dynamic source of micronutrients to coastal oceanic ecosystems in the polar regions.

Figure caption: Leverett Glacier (Greenland Ice Sheet) and Mercer Subglacial Lake (Antarctic Ice Sheet) dissolved elemental concentrations (<0.45 µm) normalized to mean non-glacial riverine trace element concentrations (Gaillardet et al., 2014) and major element concentrations (Martin and Meybeck, 1979). Grey regions indicate ±50 % of the riverine mean. Although major elements can be significantly depleted compared to non-glacial rivers, trace elements are commonly similar to or enriched.

 

Authors:
Jon R. Hawkings (Florida State Univ and German Research Centre for Geosciences)
Mark L. Skidmore (Montana State Univ)
Jemma L. Wadham (Univ of Bristol, UK)
John C. Priscu (Montana State Univ)
Peter L. Morton (Florida State Univ)
Jade E. Hatton (Univ of Bristol, UK)
Christopher B. Gardner (Ohio State Univ)
Tyler J. Kohler (École Polytechnique Fédérale de Lausanne, Switzerland)
Marek Stibal (Charles University, Prague, Czech Republic)
Elizabeth A. Bagshaw (Cardiff Univ, UK)
August Steigmeyer (Montana State Univ)
Joel Barker (Univ of Minnesota)
John E. Dore (Montana State Univ)
W. Berry Lyons (Ohio State Univ)
Martyn Tranter (Univ of Bristol, UK)
Robert G. M. Spencer (Florida State Univ)
SALSA Science Team

When GEOTRACES‐based synthesis efforts improve global iron-cycling understanding

Posted by mmaheigan 
· Friday, December 18th, 2020 

Authors of a recent paper published in Global Biogeochemical Cycles conducted a detailed study of the residence times of total and dissolved iron (Fe) in the upper layers (0-250m) of the global ocean. Using historical (1980-2007) and recent GEOTRACES data, they compiled an impressive data set comprising dissolved, filtered and trap-collected particulate Fe spanning different biogeochemical oceanographic provinces. They also used indirect isotopic approaches to calculate Fe export from the surface layers (e.g., based on thorium-234-uranium-238 disequilibrium). The study revealed that upper ocean residence times of total Fe consistently fell between 10 and 100 days, despite a broad range of total Fe inventories and ocean biogeochemical settings. Conversely, dissolved Fe residences times were longer and more variable, cycling on sub annual to annual time scales. In addition to these detailed insights on upper ocean Fe cycling, these new data sets will help constrain the rate constant for total Fe export, an important term for exploring links between ocean Fe cycling and the global carbon cycle in ocean biogeochemical models.

Figure Caption: In-situ iron concentration and export (Ftot) estimates from numerous GEOTRACES efforts were combined with prior study results to constrain the residence time of iron in the upper ocean (diagonal lines, lower panel). Broad patterns in iron residence times emerged when contrasting coastal and open regions (pink vs. white), as well as with high and low latitude zones (black vs. white). Despite clear regional differences, however, the majority of residence times for total iron fell into a small range between 10 and 100 days.

 

Authors:
E. E. Black (former WHOI, current Dalhousie University, Lamont Doherty Earth Observatory)
S. S. Kienast (Dalhousie University)
N. Lemaitre (Institute of Geochemistry and Petrology, Zürich, Switzerland)
P. J. Lam (University of California, Santa Cruz)
R. F. Anderson (Lamont Doherty Earth Observatory)
H. Planquette (University Brest)
F. Planchon (University Brest)
K. O. Buesseler (WHOI)

This is a joint highlight with GEOTRACES

Partitioning carbon export into particulate and dissolved pools from biogeochemical profiling float observations

Posted by mmaheigan 
· Thursday, December 17th, 2020 

Carbon export from the surface into the deep ocean via the biological pump is a significant sink for atmospheric carbon dioxide. The relative contributions of sinking particles—particulate organic carbon (POC) and dissolved organic carbon (DOC)—to the total export affect the efficiency of carbon export.

In a recent study published in Global Biogeochemical Cycles, the authors used measurements from biogeochemical profiling floats in the Northeast Pacific from 2009 to 2017 to estimate net community production (NCP), an analog for carbon export. In order to close three tracer budgets (nitrate, dissolved inorganic carbon, and total alkalinity), the authors combined these float measurements with data from the Ocean Station Papa mooring and recently developed algorithms for carbonate system parameters. By constraining end-member nutrient ratios of the POC and DOC produced, this multi-tracer approach was used to estimate regional NCP across multiple depth horizons throughout the annual cycle, partition NCP into the POC and DOC contributions, and calculate particulate inorganic carbon (PIC) production, a known ballast material for sinking particles (Figure 1). The authors also estimated POC attenuation with depth, POC export across deeper horizons, and in situ export efficiency via a particle backscatter-based approach.

With the advent of “fully-loaded” biogeochemical profiling floats equipped with nitrate, oxygen, pH and bio-optical sensors, this approach may be used to assess the magnitude and efficiency of carbon export in other ocean regions from a single platform, which will greatly reduce the risks and costs associated with traditional ship-based measurements, while broadening the spatiotemporal scales of observation.

Figure caption: Climatological mean NCP (blue line) over the entire study period (2009-2017); the POC portion of NCP (filled blue area), the DOC portion (white space) and PIC production rate (red line), in the mixed layer (left), and the euphotic zone (right). The numbers in parentheses are the integrated annual NCP rates for each curve and uncertainty reported was determined using a Monte Carlo approach.

 

Authors:
William Haskell (MBARI, now Mote Marine Laboratory)
Andrea Fassbender (MBARI, now PMEL)
Jacki Long (MBARI)
Joshua Plant (MBARI)

How zooplankton control carbon export in the Southern Ocean

Posted by mmaheigan 
· Thursday, December 3rd, 2020 

The Southern Ocean exhibits an inverse relationship between surface primary production and export flux out of the euphotic zone. The causes of this production-export decoupling are still under debate. A recently published mini review in Frontiers in Marine Science focused on zooplankton, an important component of Southern Ocean food webs and the biological pump. The authors compared carbon export regimes from the naturally iron-fertilised Kerguelen Plateau (high surface production, but generally low export) with the iron-limited and less productive high nutrient, low chlorophyll (HNLC) waters south of Australia, where carbon export is relatively high.

Figure 1: The role of zooplankton in establishing the characteristic export regimes at two sites in the Southern Ocean, (a) the highly productive northern Kerguelen Plateau, which exhibits low export, and (b) the iron-limited waters south of Australia with low production, but relatively high carbon export.

Size structure and zooplankton grazing pressure are found to shape carbon export at both sites. On the Kerguelen Plateau, a large size spectrum of zooplankton acts as “gate-keeper” to the mesopelagic by significantly reducing the sinking flux of phytoaggregates, which establishes the characteristic low export regime. In the HNLC waters, however, the zooplankton community is low in biomass and grazes predominantly on smaller particles, which leaves the larger particles for export and leads to relatively high export flux.

Gaps in knowledge related to insufficient seasonal data coverage, understudied carbon flux pathways, and associated mesopelagic processes limit our current understanding of carbon transfer through the water column and export. More integrated data collection efforts, including the use of autonomous profiling floats (e.g., BGC-Argo), stationary moorings, etc., will improve seasonal carbon flux data coverage, thus enabling more reliable estimation of carbon export and storage in the Southern Ocean and improved projection of future changes in carbon uptake and atmospheric carbon dioxide levels.

 

Authors:
Svenja Halfter (University of Tasmania)
Emma Cavan (Imperial College London)
Ruth Eriksen (CSIRO)
Kerrie Swadling (University of Tasmania)
Philip Boyd (University of Tasmania)

Water clarity impacts temperature and biogeochemistry in Chesapeake Bay

Posted by mmaheigan 
· Thursday, December 3rd, 2020 

Estuarine water clarity is determined by suspended materials in the water, including colored dissolved organic matter, phytoplankton, sediment, and detritus. These constituents directly affect temperature because when water is opaque, sunlight heats only the shallowest layers near the surface, but when water is clear, sunlight can penetrate deeper, warming the waters below the surface. Despite the importance of accurately predicting temperature variability, many numerical modeling studies do not adequately parameterize this fundamental relationship between water clarity and temperature.

In a recent study published in Estuaries and Coasts, the authors quantified the impact of a more realistic representation of water clarity in a hydrodynamic-biogeochemical model of the Chesapeake Bay by comparing two simulations: (1) water clarity is constant in space and time for the calculation of solar heating vs. (2) water clarity varies with modeled concentrations of light-attenuating materials. In the variable water clarity simulation (2), the water is more opaque, particularly in the northern region of the Bay. During the spring and summer months, the lower water clarity in the northern Bay is associated with warmer surface temperatures and colder bottom temperatures. Warmer surface temperatures encourage phytoplankton growth and nutrient uptake near the head of the Bay, thus fewer nutrients are transported downstream. These conditions are exacerbated during high-river flow years, when differences in temperature, nutrients, phytoplankton, and zooplankton extend further seaward.

Figure 1: Top row: Difference in the light attenuation coefficient for shortwave heating, kh[m-1] (variable minus constant light attenuation simulation). June, July, and August average for (A) 2001, (B) average of 2001-2005, and (C) 2003; difference in bottom temperatures [oC] (variable minus constant). Bottom row: Difference in June, July, and August average bottom temperature for (D) 2001, (E) average of 2001-2005, and (F) 2003. Data for 2001 are representative of low river discharge, and 2003 are representative high river discharge years.

This work demonstrates that a constant light attenuation scheme for heating calculations in coupled hydrodynamic-biogeochemical models underestimates temperature variability, both temporally and spatially. This is an important finding for researchers who use models to predict future temperature variability and associated impacts on biogeochemistry and species habitability.

 

Authors:
Grace E. Kim (NASA, Goddard Space Flight Center)
Pierre St-Laurent (VIMS, William & Mary)
Marjorie A.M. Friedrichs (VIMS, William & Mary)
Antonio Mannino (NASA, Goddard Space Flight Center)

Tiny phytoplankton seen from space

Posted by mmaheigan 
· Thursday, November 19th, 2020 

Picophytoplankton, the smallest phytoplankton on Earth, are dominant in over half of the global surface ocean, growing in low-nutrient “ocean deserts” where diatoms and other large phytoplankton have difficult to thrive. Despite their small size, picophytoplankton collectively account for well over 50% of primary production in oligotrophic waters, thus playing a major role in sustaining marine food webs.

In a recent paper published in Optics Express, the authors use satellite-detected ocean color (namely remote-sensing reflectance, Rrs(λ)) and sea surface temperature to estimate the abundance of the three picophytoplankton groups—the cyanobacteria Prochlorococcus and Synechococcus, and autotrophic picoeukaryotes. The authors analysed Rrs(λ) spectra using principal component analysis, and principal component scores and SST were used in the predictive models. Then, they trained and independently evaluated the models with in-situ data from the Atlantic Ocean (Atlantic Meridional Transect cruises). This approach allows for the satellite detection of the succession of species across ocean oligotrophic ecosystem boundaries, where these cells are most abundant (Figure 1).

Figure 1. Cell abundances of the three major picophytoplankton groups (the cyanobacteria Prochlorococcus and Synechococcus, and a collective group of autotrophic picoeukaryotes) in surface waters of the Atlantic Ocean. Abundances are shown for the dominant group in terms of total biovolume (converted from cell abundance).

Since these organisms can be used as proxies for marine ecosystem boundaries, this method can be used in studies of climate and ecosystem change, as it allows a synoptic observation of changes in picophytoplankton distributions over time and space. For exploring spectral features in hyperspectral Rrs(λ) data, the implementation of this model using data from future hyperspectral satellite instruments such as NASA PACE’s Ocean Color Instrument (OCI) will extend our knowledge about the distribution of these ecologically relevant phytoplankton taxa. These observations are crucial for broad comprehension of the effects of climate change in the expansion or shifts in ocean ecosystems.

 

Authors:
Priscila K. Lange (NASA Goddard Space Flight Center / Universities Space Research Association / Blue Marble Space Institute of Science)
Jeremy Werdell (NASA Goddard Space Flight Center)
Zachary K. Erickson (NASA Goddard Space Flight Center)
Giorgio Dall’Olmo (Plymouth Marine Laboratory)
Robert J. W. Brewin (University of Exeter)
Mikhail V. Zubkov (Scottish Association for Marine Science)
Glen A. Tarran (Plymouth Marine Laboratory)
Heather A. Bouman (University of Oxford)
Wayne H. Slade (Sequoia Scientific, Inc)
Susanne E. Craig (NASA Goddard Space Flight Center / Universities Space Research Association)
Nicole J. Poulton (Bigelow Laboratory for Ocean Sciences)
Astrid Bracher (Alfred-Wegener-Institute Helmholtz Center for Polar and Marine Research / University of Bremen)
Michael W. Lomas (Bigelow Laboratory for Ocean Sciences)
Ivona Cetinić (NASA Goddard Space Flight Center / Universities Space Research Association)

 

A new Regional Earth System Model of the Mediterranean Sea biogeochemical dynamics

Posted by mmaheigan 
· Thursday, November 19th, 2020 

The Mediterranean Sea is a semi-enclosed mid-latitude oligotrophic basin with a lower net primary production than the global ocean. A west-east productivity trophic gradient results from the superposition of biogeochemical and physical processes, including the biological pump and associated carbon and nutrient (nitrogen, phosphorus) fluxes, the spatial asymmetric distribution of nutrient sources (rivers, atmospheric deposition, coastal upwelling, etc.), the estuarine inverse circulation associated with the inflow of Atlantic water through the Gibraltar Strait. The complex and highly variable interface between land and sea throughout this basin add a further layer of complexity in the Mediterranean oceanic and atmospheric circulation and on the associated biogeochemistry dynamics, emphasizing the need for high-resolution truly integrated Regional Earth System Models to track and understand fine-scale processes and ecosystem dynamics.

In a recent paper published in the Journal of Advances in Modeling Earth System, the authors introduced a new version of the Regional Earth System model RegCM-ES and evaluated its performance in the Mediterranean region. RegCM-ES fully integrates the regional climate model RegCM4, the land surface scheme CLM4.5 (Community Land Model), the river routing model HD (Hydrological Discharge Model), the ocean model MITgcm (MIT General Circulation model) and the Biogeochemical Flux Model BFM.

A comparison with available observations has shown that RegCM-ES was able to capture the mean climate of the region and to reproduce horizontal and vertical patterns of chlorophyll-a and PO4 (the limiting nutrient in the basin) (Figure 1). The same comparison revealed a systematic underestimation of simulated dissolved oxygen (which will be fixed by the use of a new parametrization of oxygen solubility), and an overestimation of NO3, possibly due to uncertainties in initial and boundary conditions (mostly traced to river and Dardanelles nutrient discharges) and an overly vigorous vertical mixing simulated by the ocean model in some parts of the Basin.

Figure.1 Distributions of chlorophyll-a mg/m3 (top) and PO4 mmol/m3 (bottom) in the Mediterranean Sea as simulated by RegCM-ES.

Overall, this analysis has demonstrated that RegCM-ES has the capabilities required to become a powerful tool for studying regional dynamics and impacts of climate change on the Mediterranean Sea and other ocean basins around the world.

 

Authors:
Marco Reale (Abdus Salam International Centre for theoretical physics-ICTP, National Institute of Oceanography and Experimental Geophysics-OGS)
Filippo Giorgi (Abdus Salam International Centre for theoretical physics-ICTP)
Cosimo Solidoro (National Institute of Oceanography and Experimental Geophysics-OGS)
Valeria Di Biagio (National Institute of Oceanography and Experimental Geophysics-OGS)
Fabio Di Sante (Abdus Salam International Centre for theoretical physics-ICTP)
Laura Mariotti (National Institute of Oceanography and Experimental Geophysics-OGS)
Riccardo Farneti (Abdus Salam International Centre for theoretical physics-ICTP)
Gianmaria Sannino (Italian National Agency for New Technologies, Energy and Sustainable Economic Development-ENEA)

Warming counteracts acidification in temperate crustose coralline algae communities

Posted by mmaheigan 
· Friday, November 6th, 2020 

Seawater carbonate chemistry has been altered by dramatic increases in anthropogenic CO2 release and global temperatures, leading to significant changes in rocky shore habitats and the metabolism of most marine organisms. There has been recent interest in how these anthropogenic stresses affect crustose coralline algae (CCA) communities because CCA photosynthesis and calcification are directly influenced by seawater carbonate chemistry. CCA is a foundation species in temperate macroalgal communities, where species succession and rocky shore community structure are particularly susceptible to anthropogenic disturbance. In particular, the disappearance of turf and foliose macroalgae caused by climate change and herbivore pressure results in the dominance of CCA (Figure 1a).

Figure 1: (a) Examples of crustose coralline algae (CCA)-dominated seaweed bed in the East Sea of Korea showing barren ground dominated by CCA (bright white and pink color on the rock; see arrows) on a rocky subtidal zone grazed by sea urchins. (b) Specific growth rate of marginal encrusting area under future climate conditions.

In a recent study published in Marine Pollution Bulletin, the authors conducted a mesocosm experiment to investigate the sensitivity of temperate CCA Chamberlainium sp. to future climate stressors, as simulated by three experimental treatments: 1) Acidification: doubled CO2; 2) Warming: +5ºC; and 3) Greenhouse: doubled CO2 and +5ºC. After a 47-day acclimation period, when compared with present-day (control: 490 μatm and 20ºC) conditions, the Acidification treatment showed decreased photosynthesis rates of Chamberlainium sp, whereas the Warming treatment showed increased photosynthesis. The Acidification treatment also showed reduced encrusting growth rates relative to the Control, but when acidification was combined with warming in the Greenhouse treatment, encrusting growth rates increased substantially (Figure 1b). Taken together, these results suggest that the negative ecophysiological responses of Chamberlainium sp to acidification are ameliorated by elevated temperatures in a greenhouse world. In other words, if the foliose macroalgal community responses negatively in the greenhouse environment, the dominance of CCA will increase further, and the biodiversity of the algae community will be reduced.

 

Authors:
Ju-Hyoung Kim (Faculty of Marine Applied Biosciences, Kunsan National University)
Il-Nam Kim (Department of Marine Science, Incheon National University)

Timing matters: Correcting float-based measurements of diurnal oxygen variability

Posted by mmaheigan 
· Friday, November 6th, 2020 

Despite its fundamental importance to the global carbon cycle, climate, and marine ecosystems, oceanic primary production is grossly under-sampled. Autonomous platforms represent an important frontier for expanding measurements of marine primary productivity in time and space, but this requires the establishment of robust, standardized methods to obtain reliable data from these platforms. Using data from profiling floats deployed in the northern Gulf of Mexico, authors of a recent study published in Biogeosciences demonstrated, for the first time, that daily cycles of dissolved oxygen can be observed with Argo-type profiling floats. The floats were instructed to profile continuously, resulting in about one profile every three hours. The floats recorded data both on the ascent (upcast) and the descent (downcast). Adjacent casts showed hysteresis in gradient areas, i.e. a lag in the concentration measurement, due to the slow response time of oxygen sensors.

Figure 1: Example of raw oxygen measurements from a downcast (dark purple line) and an upcast (dark green line) and corrected profiles (lighter purple and green lines) in (a) density and (b) pressure coordinates. (c) Upcasts and downcasts (top 150 m) plotted against each other with raw data (purple) and data corrected according to the new method (red). (d) The root-mean-square difference (RMSD) between the upcast and downcast after correcting casts for a range of time constants (τ), showing an optimal τ value in this case of 76 s (red dot).

To correct for these measurement errors, the authors developed a method to determine sensor response time in situ, using an established process for correcting sensor response time errors. This method requires a timestamp associated with each observation. The response time parameter (τ) was determined by correcting consecutive profiles taken in opposite directions using a range of possible values and finding the minimum root-mean-square-difference between them (Figure 1). In light of these findings, future oxygen measurements from Argo floats should be transmitted with time stamps for a calibration period during which up- and downcasts are recorded to facilitate response time correction. The method developed here will contribute to more accurate measurement of dissolved oxygen, thus improving the quality of derived quantities such as primary productivity.

 

Authors
Christopher Gordon (Dalhousie University)
Katja Fennel (Dalhousie University)
Clark Richards (Fisheries and Oceans Canada)
Nick Shay (University of Miami)
Jodi Brewster (University of Miami)

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fluxes export production extreme events faecal pellets fecal pellets filter feeders filtration rates fire fish Fish carbon fisheries fishing floats fluid dynamics fluorescence food webs forage fish forams freshening freshwater frontal zone functional role future oceans gelatinous zooplankton geochemistry geoengineering geologic time GEOTRACES glaciers gliders global carbon budget global ocean global warming go-ship grazing greenhouse gas greenhouse gases Greenland ground truthing groundwater Gulf of Maine Gulf of Mexico Gulf Stream gyre harmful algal bloom high latitude human food human impact human well-being hurricane hydrogen hydrothermal hypoxia ice age ice cores ice cover industrial onset inland waters in situ inverse circulation ions iron iron fertilization iron limitation isotopes jellies katabatic winds kelvin waves krill kuroshio lab vs field land-ocean continuum larvaceans lateral transport LGM lidar ligands light light attenuation lipids low nutrient machine learning mangroves marine carbon cycle marine heatwave marine particles marine snowfall marshes mCDR mechanisms Mediterranean meltwater mesopelagic mesoscale mesoscale processes metagenome metals methane methods microbes microlayer microorganisms microplankton microscale microzooplankton midwater mitigation mixed layer mixed layers mixing mixotrophs mixotrophy model modeling model validation mode water molecular diffusion MPT MRV multi-decade n2o NAAMES NCP nearshore net community production net primary productivity new ocean state new technology Niskin bottle nitrate nitrogen nitrogen cycle nitrogen fixation nitrous oxide north atlantic north pacific North Sea nuclear war nutricline nutrient budget nutrient cycles nutrient cycling nutrient limitation nutrients OA observations ocean-atmosphere ocean acidification ocean acidification data ocean alkalinity enhancement ocean carbon storage and uptake ocean carbon uptake and storage ocean color ocean modeling ocean observatories ocean warming ODZ oligotrophic omics OMZ open ocean optics organic particles oscillation outwelling overturning circulation oxygen pacific paleoceanography PAR parameter optimization parasite particle flux particles partnerships pCO2 PDO peat pelagic PETM pH phenology phosphate phosphorus photosynthesis physical processes physiology phytoplankton PIC piezophilic piezotolerant plankton POC polar polar regions policy pollutants precipitation predation predator-prey prediction pressure primary productivity Prochlorococcus productivity prokaryotes proteins pteropods pycnocline radioisotopes remineralization remote sensing repeat hydrography residence time resource management respiration resuspension rivers rocky shore Rossby waves Ross Sea ROV salinity salt marsh satellite scale seafloor seagrass sea ice sea level rise seasonal seasonality seasonal patterns seasonal trends sea spray seawater collection seaweed secchi sediments sensors sequestration shelf ocean shelf system shells ship-based observations shorelines siderophore silica silicate silicon cycle sinking sinking particles size SOCCOM soil carbon southern ocean south pacific spatial covariations speciation SST state estimation stoichiometry subduction submesoscale subpolar subtropical sulfate surf surface surface ocean Synechococcus technology teleconnections temperate temperature temporal covariations thermocline thermodynamics thermohaline thorium tidal time-series time of emergence titration top predators total alkalinity trace elements trace metals trait-based transfer efficiency transient features trawling Tris trophic transfer tropical turbulence twilight zone upper ocean upper water column upwelling US CLIVAR validation velocity gradient ventilation vertical flux vertical migration vertical transport warming water clarity water mass water quality waves weathering western boundary currents wetlands winter mixing zooplankton

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