Technical Note: Could benzalkonium chloride be a suitable alternative to mercuric chloride for preservation of seawater samples?

Instrumental equipment unsuitable or unavailable for fieldwork as well as lack of ship space can necessitate the preservation of seawater samples prior to analysis in a shore-based laboratory. Mercuric chloride (HgCl2) is routinely used for such preservation, but its handling and subsequent disposal incur environmental risks and significant expense. There is therefore a strong motivation to find less hazardous alternatives. Benzalkonium chloride (BAC) has been used previously as microbial inhibitor for freshwater samples. Here, we assess the use of BAC for marine samples prior to the measurement of oxygen-to-argon (O2 / Ar) ratios, as used for the determination of biological net community production. BAC at a concentration of 50 mg dm−3 inhibited microbial activity for at least 3 days in samples tested with chlorophyll a (Chl a) concentrations up to 1 mg m−3. BAC concentrations of 100 and 200 mg dm−3 were no more effective than 50 mg dm−3 . With fewer risks to human health and the environment, and no requirement for expensive waste disposal, BAC could be a viable alternative to HgCl2 for short-term preservation of seawater samples, but is not a replacement for HgCl2 in the case of oxygen triple isotope analysis, which requires storage over weeks to months. In any event, further tests on a case-by-case basis should be undertaken if use of BAC was considered, since its inhibitory activity may depend on concentration and composition of the microbial community

Earth observation tool for monitoring coastal eutrophication

ISECA is an Interreg project running until September 2014 that aims to advance and disseminate scientific knowledge related to eutrophication in the 2Seas area (English Channel and North Sea).The main objective of ISECA is to develop a demonstration prototype of an information system for monitoring eutrophication of coastal waters.This information system combines in-situ, satellite information and models outputs

Comparison of Above-Water Seabird and TriOS Radiometers along an Atlantic Meridional Transect

The Fiducial Reference Measurements for Satellite Ocean Color (FRM4SOC) project has carried out a range of activities to evaluate and improve the state-of-the-art in ocean color radiometry. This paper described the results from a ship-based intercomparison conducted on the Atlantic Meridional Transect 27 from 23rd September to 5th November 2017. Two different radiometric systems, TriOS-Radiation Measurement Sensor with Enhanced Spectral resolution (RAMSES) and Seabird-Hyperspectral Surface Acquisition System (HyperSAS), were compared and operated side-by-side over a wide range of Atlantic provinces and environmental conditions. Both systems were calibrated for traceability to SI (Système international) units at the same optical laboratory under uniform conditions before and after the field campaign. The in situ results and their accompanying uncertainties were evaluated using the same data handling protocols. The field data revealed variability in the responsivity between TRiOS and Seabird sensors, which is dependent on the ambient environmental and illumination conditions. The straylight effects for individual sensors were mostly within ±3%. A near infra-red (NIR) similarity correction changed the water-leaving reflectance (ρw) and water-leaving radiance (Lw) spectra significantly, bringing also a convergence in outliers. For improving the estimates of in situ uncertainty, it is recommended that additional characterization of radiometers and environmental ancillary measurements are undertaken. In general, the comparison of radiometric systems showed agreement within the evaluated uncertainty limits. Consistency of in situ results with the available Sentinel-3A Ocean and Land Color Instrument (OLCI) data in the range from (400…560) nm was also satisfactory (-8% < Mean Percentage Difference (MPD) < 15%) and showed good agreement in terms of the shape of the spectra and absolute values

Fiducial Reference Measurements for Satellite Ocean Colour (FRM4SOC)

Earth observation data can help us understand and address some of the grand challenges and threats facing us today as a species and as a planet, for example climate change and its impacts and sustainable use of the Earth’s resources. However, in order to have confidence in earth observation data, measurements made at the surface of the Earth, with the intention of providing verification or validation of satellite-mounted sensor measurements, should be trustworthy and at least of the same high quality as those taken with the satellite sensors themselves. Metrology tells us that in order to be trustworthy, measurements should include an unbroken chain of SI-traceable calibrations and comparisons and full uncertainty budgets for each of the in situ sensors. Until now, this has not been the case for most satellite validation measurements. Therefore, within this context, the European Space Agency (ESA) funded a series of Fiducial Reference Measurements (FRM) projects targeting the validation of satellite data products of the atmosphere, land, and ocean, and setting the framework, standards, and protocols for future satellite validation efforts. The FRM4SOC project was structured to provide this support for evaluating and improving the state of the art in ocean colour radiometry (OCR) and satellite ocean colour validation through a series of comparisons under the auspices of the Committee on Earth Observation Satellites (CEOS). This followed the recommendations from the International Ocean Colour Coordinating Group’s white paper and supports the CEOS ocean colour virtual constellation. The main objective was to establish and maintain SI traceable ground-based FRM for satellite ocean colour and thus make a fundamental contribution to the European system for monitoring the Earth (Copernicus). This paper outlines the FRM4SOC project structure, objectives and methodology and highlights the main results and achievements of the project: (1) An international SI-traceable comparison of irradiance and radiance sources used for OCR calibration that set measurement, calibration and uncertainty estimation protocols and indicated good agreement between the participating calibration laboratories from around the world; (2) An international SI-traceable laboratory and outdoor comparison of radiometers used for satellite ocean colour validation that set OCR calibration and comparison protocols; (3) A major review and update to the protocols for taking irradiance and radiance field measurements for satellite ocean colour validation, with particular focus on aspects of data acquisition and processing that must be considered in the estimation of measurement uncertainty and guidelines for good practice; (4) A technical comparison of the main radiometers used globally for satellite ocean colour validation bringing radiometer manufacturers together around the same table for the first time to discuss instrument characterisation and its documentation, as needed for measurement uncertainty estimation; (5) Two major international side-by-side field intercomparisons of multiple ocean colour radiometers, one on the Atlantic Meridional Transect (AMT) oceanographic cruise, and the other on the Acqua Alta oceanographic tower in the Gulf of Venice; (6) Impact and promotion of FRM within the ocean colour community, including a scientific road map for the FRM-based future of satellite ocean colour validation and vicarious calibration (based on the findings of the FRM4SOC project, the consensus from two major international FRM4SOC workshops and previous literature, including the IOCCG white paper on in situ ocean colour radiometry)

Determination of the absorption coefficient of chromophoric dissolved organic matter from underway spectrophotometry

Measurements of the absorption coefficient of chromophoric dissolved organic matter (ay) are needed to validate existing ocean-color algorithms. In the surface open ocean, these measurements are challenging because of low ay values. Yet, existing global datasets demonstrate that ay could contribute between 30% to 50% of the total absorption budget in the 400–450 nm spectral range, thus making accurate measurement of ay essential to constrain these uncertainties. In this study, we present a simple way of determining ay using a commercially-available in-situ spectrophotometer operated in underway mode. The obtained ay values were validated using independent collocated measurements. The method is simple to implement, can provide measurements with very high spatio-temporal resolution, and has an accuracy of about 0.0004 m−1 and a precision of about 0.0025 m−1 when compared to independent data (at 440 nm). The only limitation for using this method at sea is that it relies on the availability of relatively large volumes of ultrapure water. Despite this limitation, the method can deliver the ay data needed for validating and assessing uncertainties in ocean-colour algorithms

Carbon sequestration in the deep Atlantic enhanced by Saharan dust

sinking rates of particulate organicmatter. Here we present a two-year time series of sediment trap observations of particulate organic carbon flux to 3,000m depth, measured directly in two locations: the dust-rich central North Atlantic gyre and the dust-poor South Atlantic gyre. We find that carbon fluxes are twice as high and a higher proportion of primary production is exported to depth in the dust-rich North Atlantic gyre. Low stable nitrogen isotope ratios suggest that high fluxes result from the stimulation of nitrogen fixation and productivity following the deposition of dust-borne nutrients. Sediment traps in the northern gyre also collected intact colonies of nitrogen-fixing Trichodesmium species. Whereas ballast in Enhanced atmospheric input of dust-borne nutrients and minerals to the remote surface ocean can potentially increase carbon uptake and sequestration at depth. Nutrients can enhance primary productivity, and mineral particles act as ballast, increasing the southern gyre is predominantly biogenic, dust-derived mineral particles constitute the dominant ballast element during the enhanced carbon fluxes in the northern gyre. We conclude that dust deposition increases carbon sequestration in the North Atlantic gyre through the fertilization of the nitrogen-fixing community in surface waters and mineral ballasting of sinking particles

Intravenous digoxin as a bioavailability standard

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/116960/1/cpt1975171117.pd

Determination of the absorption coefficient of chromophoric dissolved organic matter from underway spectrophotometry

This is the final version. Available on open access from Optical Society of America via the DOI in this recordMeasurements of the absorption coefficient of chromophoric dissolved organic matter (ay) are needed to validate existing ocean-color algorithms. In the surface open ocean, these measurements are challenging because of low ay values. Yet, existing global datasets demonstrate that ay could contribute between 30% to 50% of the total absorption budget in the 400-450 nm spectral range, thus making accurate measurement of ay essential to constrain these uncertainties. In this study, we present a simple way of determining ay using a commercially-available in-situ spectrophotometer operated in underway mode. The obtained ay values were validated using independent collocated measurements. The method is simple to implement, can provide measurements with very high spatio-temporal resolution, and has an accuracy of about 0.0004 m−1 and a precision of about 0.0025 m−1 when compared to independent data (at 440 nm). The only limitation for using this method at sea is that it relies on the availability of relatively large volumes of ultrapure water. Despite this limitation, the method can deliver the ay data needed for validating and assessing uncertainties in ocean-colour algorithms.European Space Agency (ESA)National Atmospheric and Space Administration (NASA

Effects of elevated CO2 and temperature on phytoplankton community biomass, species composition and photosynthesis during an experimentally induced autumn bloom in the western English Channel

The combined effects of elevated pCO2 and temperature were investigated during an experimentally induced autumn phytoplankton bloom in vitro sampled from the western English Channel (WEC). A full factorial 36-day microcosm experiment was conducted under year 2100 predicted temperature (+4.5°C) and pCO2 levels (800μatm). Over the experimental period total phytoplankton biomass was significantly influenced by elevated pCO2. At the end of the experiment, biomass increased 6.5-fold under elevated pCO2 and 4.6-fold under elevated temperature relative to the ambient control. By contrast, the combined influence of elevated pCO2 and temperature had little effect on biomass relative to the control. Throughout the experiment in all treatments and in the control, the phytoplankton community structure shifted from dinoflagellates to nanophytoplankton . At the end of the experiment, under elevated pCO2 nanophytoplankton contributed 90% of community biomass and was dominated by Phaeocystis spp. Under elevated temperature, nanophytoplankton comprised 85% of the community biomass and was dominated by smaller nanoflagellates. In the control, larger nanoflagellates dominated whilst the smallest nanophytoplankton contribution was observed under combined elevated pCO2 and temperature ( ∼ 40%). Under elevated pCO2, temperature and in the control there was a significant decrease in dinoflagellate biomass. Under the combined effects of elevated pCO2 and temperature, dinoflagellate biomass increased and was dominated by the harmful algal bloom (HAB) species, Prorocentrum cordatum. At the end of the experiment, chlorophyll a (Chl a) normalised maximum photosynthetic rates (PBm) increased &gt; 6-fold under elevated pCO2 and &gt; 3-fold under elevated temperature while no effect on PBm was observed when pCO2 and temperature were elevated simultaneously. The results suggest that future increases in temperature and pCO2 simultaneously do not appear to influence coastal phytoplankton productivity but significantly influence community composition during autumn in the WEC

Performance of Ocean Colour Chlorophyll a algorithms for Sentinel-3 OLCI, MODIS-Aqua and Suomi-VIIRS in open-ocean waters of the Atlantic

This is the final version. Available on open access from Elsevier via the DOI in this recordThe proxy for phytoplankton biomass, Chlorophyll a (Chl a), is an important variable to assess the health and state of the oceans which are under increasing anthropogenic pressures. Prior to the operational use of satellite ocean-colour Chl a to monitor the oceans, rigorous assessments of algorithm performance are necessary to select the most suitable products. Due to their inaccessibility, the oligotrophic open-ocean gyres are under-sampled and therefore under-represented in global in situ data sets. The Atlantic Meridional Transect (AMT) campaigns fill the sampling gap in Atlantic oligotrophic waters. In-water underway spectrophotometric data were collected on three AMT field campaigns in 2016, 2017 and 2018 to assess the performance of Sentinel-3A (S3-A) and Sentinel-3B (S3-B) Ocean and Land Colour Instrument (OLCI) products. Three Chl a algorithms for OLCI were compared: Processing baseline (pb) 2, which uses the ocean colour 4 band ratio algorithm (OC4Me); pb 3 (OL_L2M.003.00) which uses OC4Me and a colour index (CI); and POLYMER v4.8 which models atmosphere and water reflectance and retrieves Chl a as a part of its spectral matching inversion. The POLYMER Chl a for S-3A OLCI performed best. The S-3A OLCI pb 2 tended to under-estimate Chl a especially at low concentrations, while the updated OL_L2M.003.00 provided significant improvements at low concentrations. OLCI data were also compared to MODIS-Aqua (R2018 processing) and Suomi-NPP VIIRS standard products. MODIS-Aqua exhibited good performance similar to OLCI POLYMER whereas Suomi-NPP VIIRS exhibited a slight under-estimate at higher Chl a values. The reasons for the differences were that S-3A OLCI pb 2 Rrs were over-estimated at blue bands which caused the under-estimate in Chl a. There were also some artefacts in the Rrs spectral shape of VIIRS which caused Chl a to be under-estimated at values >0.1 mg m-3. In addition, using in situ Rrs to compute Chl a with OC4Me we found a bias of 25% for these waters, related to the implementation of the OC4ME algorithm for S-3A OLCI. By comparison, the updated OLCI processor OL_L2M.003.00 significantly improved the Chl a retrievals at lower concentrations corresponding to the AMT measurements. S-3A and S-3B OLCI Chl a products were also compared during the Sentinel-3 mission tandem phase (the period when S-3A and S-3B were flying 30 sec apart along the same orbit). Both S-3A and S-3B OLCI pb 2 under-estimated Chl a especially at low values and the trend was greater for S-3A compared to S-3B. The performance of OLCI was improved by using either OL_L2M.003.00 or POLYMER Chl a. Analysis of coincident satellite images for S-3A OLCI, MODIS-Aqua and VIIRS as composites and over large areas illustrated that OLCI POLYMER gave the highest Chl a concentrations and percentage (%) coverage over the north and south Atlantic gyres, and OLCI pb 2 produced the lowest Chl a and % coverage.European Space Agency (ESA)Natural Environment Research Council (NERC)National Centre for Earth Observation (NCEO