Metadata Report for BODC Series Reference Number 1625083

• Metadata Summary

• Problem Reports

• Data Access Policy

• Narrative Documents

• Project Information

• Data Activity or Cruise Information

• Fixed Station Information

• BODC Quality Flags

• SeaDataNet Quality Flags

Metadata Summary

Problem Reports

No Problem Report Found in the Database

Data quality report for DY033 PAR CTD data

The data recorded in the first few surface bins in the PAR channel have been flagged in several series, due to unrealistic values which exceeded the maximum permissible value for the parameter (500 W m^-2). Although flags have only been applied in series where the maximum PAR value is above this level, the presence of several CTD casts with surface PAR values in excess of 500 W m^-2 could indicate a wider problem with the data from this channel. Therefore BODC recommend that the data from this channel are used with caution.

Data Access Policy

Open Data supplied by Natural Environment Research Council (NERC)

You must always use the following attribution statement to acknowledge the source of the information: "Contains data supplied by Natural Environment Research Council."

Narrative Documents

Sea-Bird Dissolved Oxygen Sensor SBE 43 and SBE 43F

The SBE 43 is a dissolved oxygen sensor designed for marine applications. It incorporates a high-performance Clark polarographic membrane with a pump that continuously plumbs water through it, preventing algal growth and the development of anoxic conditions when the sensor is taking measurements.

Two configurations are available: SBE 43 produces a voltage output and can be incorporated with any Sea-Bird CTD that accepts input from a 0-5 volt auxiliary sensor, while the SBE 43F produces a frequency output and can be integrated with an SBE 52-MP (Moored Profiler CTD) or used for OEM applications. The specifications below are common to both.

Specifications

Further details can be found in the manufacturer's specification sheet.

Instrument Description for DY033 Stainless Frame CTD

CTD Unit and Auxiliary Sensors

The CTD unit comprised a Sea-Bird Electronics (SBE) 9plus underwater unit, an SBE 11plus deck unit, a NOC-S stainless steel 24-way frame and 24 10 L OTE Water Samplers; all of which were mounted on a stainless steel 24-way CTD frame. Attached to the CTD were two SBE 3P temperature sensors, two SBE 4C conductivity sensors, one Paroscientific Digiquartz pressure sensor, one SBE 43 dissolved oxygen sensor, two Biospherical QCP Cosine PAR sensors, one WETLabs BBRTD light scattering sensor, one Benthos 916T altimeter one CTG Aquatracka MKIII fluorometer, one CTG Alphatracka MKII transmissometer and one downwards facing Workhorse Monitor 300 Khz LADCP.

The dissolved oxygen sensor failed during cast 074 was replaced following cast 075 with a backup sensor.

Sea-Bird Electronics SBE 911 and SBE 917 series CTD profilers

The SBE 911 and SBE 917 series of conductivity-temperature-depth (CTD) units are used to collect hydrographic profiles, including temperature, conductivity and pressure as standard. Each profiler consists of an underwater unit and deck unit or SEARAM. Auxiliary sensors, such as fluorometers, dissolved oxygen sensors and transmissometers, and carousel water samplers are commonly added to the underwater unit.

Underwater unit

The CTD underwater unit (SBE 9 or SBE 9 plus) comprises a protective cage (usually with a carousel water sampler), including a main pressure housing containing power supplies, acquisition electronics, telemetry circuitry, and a suite of modular sensors. The original SBE 9 incorporated Sea-Bird's standard modular SBE 3 temperature sensor and SBE 4 conductivity sensor, and a Paroscientific Digiquartz pressure sensor. The conductivity cell was connected to a pump-fed plastic tubing circuit that could include auxiliary sensors. Each SBE 9 unit was custom built to individual specification. The SBE 9 was replaced in 1997 by an off-the-shelf version, termed the SBE 9 plus, that incorporated the SBE 3 plus (or SBE 3P) temperature sensor, SBE 4C conductivity sensor and a Paroscientific Digiquartz pressure sensor. Sensors could be connected to a pump-fed plastic tubing circuit or stand-alone.

Temperature, conductivity and pressure sensors

The conductivity, temperature, and pressure sensors supplied with Sea-Bird CTD systems have outputs in the form of variable frequencies, which are measured using high-speed parallel counters. The resulting count totals are converted to numeric representations of the original frequencies, which bear a direct relationship to temperature, conductivity or pressure. Sampling frequencies for these sensors are typically set at 24 Hz.

The temperature sensing element is a glass-coated thermistor bead, pressure-protected inside a stainless steel tube, while the conductivity sensing element is a cylindrical, flow-through, borosilicate glass cell with three internal platinum electrodes. Thermistor resistance or conductivity cell resistance, respectively, is the controlling element in an optimized Wien Bridge oscillator circuit, which produces a frequency output that can be converted to a temperature or conductivity reading. These sensors are available with depth ratings of 6800 m (aluminium housing) or 10500 m (titanium housing). The Paroscientific Digiquartz pressure sensor comprises a quartz crystal resonator that responds to pressure-induced stress, and temperature is measured for thermal compensation of the calculated pressure.

Additional sensors

Optional sensors for dissolved oxygen, pH, light transmission, fluorescence and others do not require the very high levels of resolution needed in the primary CTD channels, nor do these sensors generally offer variable frequency outputs. Accordingly, signals from the auxiliary sensors are acquired using a conventional voltage-input multiplexed A/D converter (optional). Some Sea-Bird CTDs use a strain gauge pressure sensor (Senso-Metrics) in which case their pressure output data is in the same form as that from the auxiliary sensors as described above.

Deck unit or SEARAM

Each underwater unit is connected to a power supply and data logging system: the SBE 11 (or SBE 11 plus) deck unit allows real-time interfacing between the deck and the underwater unit via a conductive wire, while the submersible SBE 17 (or SBE 17 plus) SEARAM plugs directly into the underwater unit and data are downloaded on recovery of the CTD. The combination of SBE 9 and SBE 17 or SBE 11 are termed SBE 917 or SBE 911, respectively, while the combinations of SBE 9 plus and SBE 17 plus or SBE 11 plus are termed SBE 917 plus or SBE 911 plus.

Specifications

Specifications for the SBE 9 plus underwater unit are listed below:

Further details can be found in the manufacturer's specification sheet.

Chelsea Technologies Group Aquatracka MKIII fluorometer

The Chelsea Technologies Group Aquatracka MKIII is a logarithmic response fluorometer. Filters are available to enable the instrument to measure chlorophyll, rhodamine, fluorescein and turbidity.

It uses a pulsed (5.5 Hz) xenon light source discharging along two signal paths to eliminate variations in the flashlamp intensity. The reference path measures the intensity of the light source whilst the signal path measures the intensity of the light emitted from the specimen under test. The reference signal and the emitted light signals are then applied to a ratiometric circuit. In this circuit, the ratio of returned signal to reference signal is computed and scaled logarithmically to achieve a wide dynamic range. The logarithmic conversion accuracy is maintained at better than one percent of the reading over the full output range of the instrument.

Two variants of the instrument are available, both manufactured in titanium, capable of operating in depths from shallow water down to 2000 m and 6000 m respectively. The optical characteristics of the instrument in its different detection modes are visible below:

* The wavelengths for the turbidity filters are customer selectable but must be in the range 400 to 700 nm. The same wavelength is used in the excitation path and the emission path.

The instrument measures chlorophyll a, rhodamine and fluorescein with a concentration range of 0.01 µg l^-1 to 100 µg l^-1. The concentration range for turbidity is 0.01 to 100 FTU (other wavelengths are available on request).

The instrument accuracy is ± 0.02 µg l^-1 (or ± 3% of the reading, whichever is greater) for chlorophyll a, rhodamine and fluorescein. The accuracy for turbidity, over a 0 - 10 FTU range, is ± 0.02 FTU (or ± 3% of the reading, whichever is greater).

Further details are available from the Aquatracka MKIII specification sheet.

Biospherical Instruments Log Quantum Cosine Irradiance Sensor QCP-2300 & QCP-2350

The QCP-2300 is a submersible cosine-collector radiometer designed to measure irradiance over Photosynthetically Active Radiation (PAR) wavelengths. It features a constant (better than ±10%) quantum response from 400 to 700 nm with the response being sharply attenuated above 700 nm and below 400 nm.

The sensor is a blue-enhanced high stability silicon photovoltaic detector with dielectric and absorbing glass filter assembly. The output is a DC voltage typically between 0 and 5 VDC that is proportional to the log of the incident irradiance.

The QCP-2300 is specifically designed for integration with 12-bit CTD systems and dataloggers requiring a limited-range of signal input.

Specifications

Further details can be found in the manufacturer's manual.

Chelsea Technologies Group ALPHAtracka and ALPHAtracka II transmissometers

The Chelsea Technologies Group ALPHAtracka (the Mark I) and its successor, the ALPHAtracka II (the Mark II), are both accurate (< 0.3 % fullscale) transmissometers that measure the beam attenuation coefficient at 660 nm. Green (565 nm), yellow (590 nm) and blue (470 nm) wavelength variants are available on special order.

The instrument consists of a Transmitter/Reference Assembly and a Detector Assembly aligned and spaced apart by an open support frame. The housing and frame are both manufactured in titanium and are pressure rated to 6000 m depth.

The Transmitter/Reference housing is sealed by an end cap. Inside the housing an LED light source emits a collimated beam through a sealed window. The Detector housing is also sealed by an end cap. A signal photodiode is placed behind a sealed window to receive the collimated beam from the Transmitter.

The primary difference between the ALPHAtracka and ALPHAtracka II is that the Alphatracka II is implemented with surface-mount technology; this has enabled a much smaller diameter pressure housing to be used while retaining exactly the same optical train as in the Mark I. Data from the Mark II version are thus fully compatible with that already obtained with the Mark I. The performance of the Mark II is further enhanced by two electronic developments from Chelsea Technologies Group - firstly, all items are locked in a signal nulling loop of near infinite gain and, secondly, the signal output linearity is inherently defined by digital circuitry only.

Among other advantages noted above, these features ensure that the optical intensity of the Mark II, indicated by the output voltage, is accurately represented by a straight line interpolation between a reading near full-scale under known conditions and a zero reading when blanked off.

For optimum measurements in a wide range of environmental conditions, the Mark I and Mark II are available in 5 cm, 10 cm and 25 cm path length versions. Output is default factory set to 2.5 volts but can be adjusted to 5 volts on request.

Further details about the Mark II instrument are available from the Chelsea Technologies Group ALPHAtrackaII specification sheet.

WETLabs Single-angle Backscattering Meter ECO BB

An optical scattering sensor that measures scattering at 117°. This angle was determined as a minimum convergence point for variations in the volume scattering function induced by suspended materials and water. The measured signal is less determined by the type and size of the materials in the water and is more directly correlated to their concentration.

Several versions are available, with minor differences in their specifications:

• ECO BB(RT)provides analog or RS-232 serial output with 4000 count range
• ECO BB(RT)D adds the possibility of being deployed in depths up to 6000 m while keeping the capabilities of ECO BB(RT)
• ECO BB provides the capabilities of ECO BB(RT) with periodic sampling
• ECO BBB is similar to ECO BB but with internal batteries for autonomous operation
• ECO BBS is similar to ECO BB but with an integrated anti-fouling bio-wiper
• ECO BBSB has the capabilities of ECO BBS but with internal batteries for autonomous operation

Specifications

Further details can be found in the manufacturer's specification sheet.

Paroscientific Absolute Pressure Transducers Series 3000 and 4000

Paroscientific Series 3000 and 4000 pressure transducers use a Digiquartz pressure sensor to provide high accuracy and precision data. The sensor comprises a quartz crystal resonator that responds to pressure-induced stress, and temperature is measured for thermal compensation of the calculated pressure.

The 3000 series of transducers includes one model, the 31K-101, whereas the 4000 series includes several models, listed in the table below. All transducers exhibit repeatability of better than ±0.01% full pressure scale, hysteresis of better than ±0.02% full scale and acceleration sensitivity of ±0.008% full scale /g (three axis average). Pressure resolution is better than 0.0001% and accuracy is typically 0.01% over a broad range of temperatures.

Differences between the models lie in their pressure and operating temperature ranges, as detailed below:

Further details can be found in the manufacturer's specification sheet.

Originator's processing document for DY033 CTD data

Sampling strategy

A total of 47 usable stainless steel frame CTD casts and 41 usable titanium frame CTD casts were performed during DY033, which sailed from Southampton on 11 July 2015 and docked in Southampton on 03 August 2015. The majority of the casts were performed at Shelf Seas Biogeochemistry process stations Candyfloss and CS2, with a further two CTD casts being performed at process station Benthic A. Further CTD casts were performed during a transect conducted between station Benthic A and the shelf edge, and in two more transects performed off the shelf edge.

CTD problems experienced during the cruise:

• The titanium frame CTD hit the bottom during cast CTD014T, resulting in an offset in the primary conductivity (and thus salinity) data. The primary conductivity sensor was changed before cast CTD021T.
• The PAR sensor was removed from the titanium frame CTD between casts CTD014T and CTD058T as it was only depth rated to 500 m.
• Casts CTD038T and CTD039T were aborted due to termination failure. Usable data was collected from CTD038T but not from CTD039T.
• On CTD057 (stainless steel frame CTD) the wire was caught in the sheave and damaged (a new termination was required). No data is available for this cast.
• On CTD074 (stainless steel frame CTD) the oxygen sensor started reading unrealistically low values (approximately 160 µ mol^-1 kg^-1). This problem persisted in cast CTD075. The oxygen sensor was subsequently replaced with the new sensor being used for casts CTD076 onwards. The oxygen channel from casts 74 and 75 has been removed from the final version of the files.
• There were problems with the data recorded by the replacement oxygen sensor on casts CTD078 and CTD090. The oxygen channel from casts CTD078 and CTD090 has been removed from the final version of the files.

Data Processing

For each CTD cast the following raw data files were generated:

• DY033_XYZ.bl (a record of bottle firing locations)
• DY033_XYZ.hdr (header file)
• DY033_XYZ.hex (raw data file)
• DY033_XYZ.con (configuration file)

where XYZ is the cast number of the CTD data series.

The following processing was performed by the Originator using the SBE Data Processing software (Seasave Version 7.23.2):

1. DatCnv was used to read in the raw CTD data file (.hex) which contained the data in engineering units and apply calibrations as appropriate through the instrument configurations (.con) file.
2. Bottle Summary was run to create a .btl file containing the average, standard deviation, min and max values recorded by the CTD instrument suite at bottle firings.
3. Wild Edit was run to remove spikes in the pressure channel.
4. Filter was run on the pressure channel to smooth out the high frequency data
5. AlignCTD was run to advance the oxygen data from both the stainless steel and titanium frame CTDs by three seconds.
6. CellTM was run using alpha = 0.03 and 1/beta = 7 (for both CTD packages), to correct for conductivity errors induced by the transfer of heat from the conductivity cell to the seawater.
7. Derive was run to create the variables Salinity, Salinity 2, Oxygen SBE 43 and Oxygen Tau correction. The output file was then saved as DY033_XYZ_derive.cnv.
8. BinAverage and Strip were run to average the data to 2Hz bins (0.5 seconds) and to remove the salinity and oxygen channels which were created when Derive was run. The output file was then saved as DY033_XYZ_derive_2Hz.cnv.

The originator then proceeded to process the data further in Matlab.

1. The data from the 2HZ and 24HZ processed CTD data files were extracted and combined with metadata from the Event log to create .mat files for each series at both 2HZ and 24 HZ resolutions.
2. Inspection of the raw turbidity data revealed that there was a bug in the Seasave DatCnv conversion module which resulted in it incorrectly converting the raw turbidity voltage into m^-1 sr^-1. Therefore, the originator re-derived turbidity manually using the following equation (SF = scale factor, DC = dark counts):

   CTDturb = CTDturb_raw x SF - (SF x DC)

3. The originator manually inspected the 2Hz data files to identify the surface soak and then cropped the 2Hz and 24Hz data files to remove the surface soak from the data.
4. The salinity, conductivity, temperature, oxygen, attenuation, turbidity and fluorescence channels in the 24Hz data files were all de-spiked using an automated routine, with the originator converting the spikes to NaN (not a number) values.
5. Further manual de-spiking was carried out to identify larger periods of bad data.
6. The 24Hz data were averaged into one decibar downcast only bins and liner interpolation was used to fill gaps in the profile.
7. All channels except PAR were smoothed further using a 10 m running median.
8. The salinity data were then calibrated using salinity samples collected by the CTD water bottles and analysed on a Guildline Autosal salinometer. The chlorophyll fluorescence and dissolved oxygen channels were calibrated against water bottle samples. A calibration could not be determined for titanium chlorophyll so this channel remains uncalibrated for the titanium frame CTD.
9. It was this calibrated version of the data which were then ingested by BODC, although all other versions have been archived and are available on request.

Field Calibrations

Salinity

A total of 93 salinity samples were collected from the stainless steel frame CTD during DY033 and analysed on a Guildline Autosal salinometer. Using all samples the mean and standard deviation of residuals were calculated as 0.0012859 ± 0.047523 for the first sensor and 0.0018212 ±0.04726 for the second sensor. After removing the outliers where the difference between the Autosal and CTD values was greater than 1 standard deviation and/or > 0.002, the mean and stand deviation of residuals were reduced to -0.0036901 ± 0.0013353 for the first sensor and -0.0030173 ± 0.001501 for the second sensor. The following regressions were then applied to the CTD salinity profiles:

Sensor 1

Bottle Salinity = 0.99794 x CTD_salinity + 0.069241

R² = 0.99994

Sensor 2:

Bottle salinity = 0.99983 x CTD_salinity + 0.0031738

R² = 0.99992

A total of 46 salinity samples were collected from titanium frame CTD during DY033 and analysed on a Guildline Autosal salinometer. Following the CTD hitting the bottom on cast CTD014T, a much larger offset was introduced into the data from the primary conductivity sensor (for casts CTD015T, CTD017T and CTD019T). The sensor was then changed before cast CTD021T. Therefore, three separate calibrations were required for the salinity data from DY034:

• One for casts CTD002T to CTD014T
• One for casts CTD015T to CTD019T
• One for casts CTD021T to CTD089T

Using all samples the mean and standard deviation of residuals for the primary sensor were calculated as -0.002075 ± 0.0028558 (CTD002T to CTD014T), +0.012975 ± 0030837 (CTD015T to CTD019T) and +0.0017941 ± 0.0042938 (CTD021T to CTD089T). The mean and standard deviation of residuals for the secondary sensor was -0.00090476 ± 0.013903. After removing the outliers where the difference between the Autosal and CTD values was greater than 1.5 standard deviations in the primary sensor (CT021T to CTD089T) and the secondary sensor, the mean and stand deviation of residuals were reduced to +0.00096562 ± 0.0025739 in the primary sensor (CTD021T to CTD089T) and +0.0012024 ± 0.0026419 for the secondary sensor. The following regressions were applied:

Sensor 1 (CTD002T to CTD014%:

Calibrated Salinity = 1.0249 x CTD salinity - 0.88376

R² = 0.99539

Number of samples = 4

Sensor 1 (CTD015T to CTD019T):

Calibrated Salinity = 1.008 x CTD salinity - 0.27126

R² = 0.99999

Number of samples = 4

Sensor 1 (CTD021T to CTD089T):

Calibrated salinity = 0.99753 x CTD_salinity + 0.08843

R² = 0.99987

Number of samples = 32

Sensor 2:

Calibrated salinity = 0.99955 x CTD_salinity + 0.017088

R² = 0.99986

Number of samples = 41

Chlorophyll

63 chlorophyll samples were collected during cruise DY034. Once all chlorophyll samples collected from the top 30 m of water during daylight hours were removed, a total of 29 chlorophyll samples remained to calibrate the CTD fluorometer attached to the stainless steel frame CTD. The originator used a linear regression to calibrate the chlorophyll fluorometer against the 29 chlorophyll samples, with the following calibration equation being used to calibrate the fluorometer:

CHL = 2.1084 x CTDfluor - 0.00007546

R² = 0.79931

Oxygen

81 oxygen samples were collected from the stainless steel frame CTD to calibrate the dissolved oxygen sensor. The originator used a linear regression to calibrate the dissolved oxygen sensor against the 81 samples, with the following calibration equation being used to calibrate the dissolved oxygen sensor:

Oxygen = 1.0148 x CTDoxy + 8.5911

R² = 0.9883

20 oxygen samples were collected from the titanium frame CTD to calibrate the dissolved oxygen sensor. The originator used a linear regression to calibrate the dissolved oxygen sensor against the 98 oxygen samples. Due to the small number of samples, the calibrated dissolved oxygen values recorded by the stainless steel frame CTD on consecutive casts were also used in the linear regression. The following calibration equation being used to calibrate the dissolved oxygen sensor:

Oxygen = 1.0038 x CTDoxy + 8.7088

R² = 0.9441

More information on the processing carried out and calibrations applied by the data originator the can be found in the data originator's CTD Processing Report.

Processing by BODC of RRS Discovery DY033 CTD data

Several versions of the CTD data recorded during DY033 arrived at BODC in the form of ASCII and Matlab (.MAT) files. In addition to the raw CTD data, BODC were provided with the 24 Hz and 2 Hz versions created at the end of the originator's Seasave processing and at each subsequent stage of Matlab processing. The fully calibrated CTD data binned to 1db downcast bins were then reformatted to BODC's internal NetCDF format, however all earlier versions of the data supplied to BODC have been archived and are available on request. The following table shows the mapping of the originator's variables to the appropriate BODC parameter codes:

The following additional parameters were derived when the data were converted into QXF format:

The reformatted data were visualised using the in-house EDSERPLO software. Suspect data were marked by adding an appropriate quality control flag, and missing data by setting the data to an appropriate value and applying the quality control flag. The secondary data channels were dropped as there was no clear difference in the quality of the data from the primary and secondary channels.

Project Information

Shelf Sea Biogeochemistry (SSB) Programme

Shelf Sea Biogeochemistry (SSB) is a £10.5 million, six-year (2011-2017) research programme, jointly funded by the Natural Environment Research Council (NERC) and the Department for Environment, Food and Rural Affairs (DEFRA). The aim of the research is to reduce the uncertainty in our understanding of nutrient and carbon cycling within the shelf seas, and of their role in global biogeochemical cycles. SSB will also provide effective policy advice and make a significant contribution to the Living with Environmental Change programme.

Background

The Shelf Sea Biogeochemistry research programme directly relates to the delivery of the NERC Earth system science theme and aims to provide evidence that supports a number of marine policy areas and statutory requirements, such as the Marine Strategy Framework Directive and Marine and Climate Acts.

The shelf seas are highly productive compared to the open ocean, a productivity that underpins more than 90 per cent of global fisheries. Their importance to society extends beyond food production to include issues of biodiversity, carbon cycling and storage, waste disposal, nutrient cycling, recreation and renewable energy resources.

The shelf seas have been estimated to be the most valuable biome on Earth, but they are under considerable stress, as a result of anthropogenic nutrient loading, overfishing, habitat disturbance, climate change and other impacts.

However, even within the relatively well-studied European shelf seas, fundamental biogeochemical processes are poorly understood. For example: the role of shelf seas in carbon storage; in the global cycles of key nutrients (nitrogen, phosphorus, silicon and iron); and in determining primary and secondary production, and thereby underpinning the future delivery of many other ecosystem services.

Improved knowledge of such factors is not only required by marine policymakers; it also has the potential to increase the quality and cost-effectiveness of management decisions at the local, national and international levels under conditions of climate change.

The Shelf Sea Biogeochemistry research programme will take a holistic approach to the cycling of nutrients and carbon and the controls on primary and secondary production in UK and European shelf seas, to increase understanding of these processes and their role in wider biogeochemical cycles. It will thereby significantly improve predictive marine biogeochemical and ecosystem models over a range of scales.

The scope of the programme includes exchanges with the open ocean (transport on and off the shelf to a depth of around 500m), together with cycling, storage and release processes on the shelf slope, and air-sea exchange of greenhouse gases (carbon dioxide and nitrous oxide).

Further details are available on the SSB website.

Participants

15 different organisations are directly involved in research for SSB. These institutions are

• Centre for Environment, Fisheries and Aquaculture Science (Cefas)
• Meteorological Office
• National Oceanography Centre (NOC)
• Plymouth Marine Laboratory (PML)
• Scottish Association for Marine Science (SAMS) / Scottish Marine Institute (SMI)
• University of Aberdeen
• University of Bangor
• University of East Anglia (UEA)
• University of Edinburgh
• University of Essex
• University of Liverpool
• University of Oxford
• Plymouth University
• University of Portsmouth
• University of Southampton

In addition, there are third party institutions carrying out sampling work for SSB, but who are not involved in the programme itself. These are:

• The Agri-Food and Biosciences Institute (AFBI)
• Irish Marine Institute (MI)
• Marine Science Scotland (MSS)

Research details

Overall, five Work Packages have been funded by the SSB programme. These are described in brief below:

• Work Package 1: Carbon and Nutrient Dynamics and Fluxes over Shelf Systems (CaNDyFloSS).
  This work package aims to perform a comprehensive study of the cycling of nutrients and carbon throughout the water column over the whole north-west European shelf. This will allow the fluxes of nutrients and carbon between the shelf and the deep ocean and atmosphere to be quantified, establishing the role of the north-west European continental shelf in the global carbon cycle.

• Work Package 2: Biogeochemistry, macronutrient and carbon cycling in the benthic layer.
  This work package aims are to map the sensitivity and status of seabed habitats, based on physical conditions, ecological community structure and the size and dynamics of the nitrogen and carbon pools found there. This information will be used, in conjunction with some laboratory-based work, to generate an understanding of the potential impacts on the benthic community as a result of changing environmental conditions, such as rising CO₂ levels.

• Work Package 3: The supply of iron from shelf sediments to the ocean.
  The research for this work package addresses the question of how currents, tides, weather and marine chemistry allow new iron to be transported away from the shallow shelf waters around the United Kingdom (UK), to the nearby open ocean. This will ultimately allow an improved understanding of how the transport of iron in shelf waters and shelf sediments influences phytoplankton growth in open oceans. This in turn improves the understanding of carbon dioxide uptake by phytoplankton.

• Work Package 4: Integrative modelling for Shelf Seas Biogeochemistry.
  The aim of this work package is the development of a new shelf seas biogeochemical model system, coupled to a state of the art physical model, that is capable of predicting regional impacts of environmental change of timescales from days to decades. It is envisaged that the combination of predictive tools and new knowledge developed in this work package will underpin development and implementation of marine policy and marine forecasting systems.

• Work Package 5: Data synthesis and management of marine and coastal carbon (DSMMAC).
  This work package is funded by Defra and is also known by the name 'Blue Carbon'. The aim is to provide a process-based, quantitative assessment of the role of UK coastal waters and shelf seas in carbon storage and release, using existing data and understanding, and also emerging results from SSB fieldwork, experiments and modelling. Particular emphasis will be given to processes that may be influenced by human activities, and hence the opportunity for management interventions to enhance carbon sequestration.

Fieldwork and data collection

The campaign consists of the core cruises in the table below, to the marine shelf (and shelf-edge) of the Celtic Sea on board the NERC research vessels RRS Discovery and RRS James Cook. These cruises will focus on the physics and biogeochemistry of the benthic and pelagic zones of the water column, primarily around four main sampling sites in this area.

Core cruises will be supplemented by partner cruises led by Cefas, MI, MSS, Bangor University and AFBI, spanning the shelf seas and shelf-edges around United Kingdom and Republic of Ireland.

Activities will include coring, Conductivity Temperature and Depth (CTD) deployments, Acoustic Doppler Current Profilers (ADCP) surveys, moorings and wire-walker deployments, benthic lander observatories, autonomous gliders and submersible surveys, Marine Snow Catcher particulate matter analysis, plankton net hauls, in-situ sediment flume investigations and laboratory incubations with core and sea water samples.

Shelf Sea Biogeochemistry (SSB) Programme Work Package 1: CaNDyFloSS

Carbon and Nutrient Dynamics and Fluxes over Shelf Systems (CaNDyFloSS) is a £2.76 million component of the Natural Environment Research Council (NERC) Shelf Sea Biogeochemistry (SSB) research programme, running from 2013 to 2017. It is jointly funded by NERC and the Department for Environment, Food and Rural Affairs (DEFRA). The aim of the research is to perform a comprehensive study of the cycling of nutrients and carbon throughout the water column over the whole north-west European shelf. This will allow the fluxes of nutrients and carbon between the shelf and the deep ocean and atmosphere to be quantified, establishing the role of the north-west European continental shelf in the global carbon cycle.

Background

Shelf seas are the primary regions of human marine resource exploitation, including both renewable and fossil fuel energy sources, recreation, trade and food production. They provide 90% of global fish catches which form an important source of food to much of the global population. They also play an important role in the ecosystem services provided by the oceans as a whole, in particular in storing carbon away from the atmosphere.

Physical and biochemical processes in shelf seas influence the removal of CO₂ from the atmosphere and the subsequent storage of carbon in the deep ocean. Biological growth draws carbon out of the water, which is then replaced by carbon in CO₂ from the atmosphere. In the shelf seas this growth is supported by terrestrial and open ocean sources of nutrients, implying intimate roles for both the terrestrial biosphere and the open ocean environment in regulating shelf sea climate services. The oceans can also be a major source or sink for other greenhouse gases, including nitrous oxide (N₂O), with the shallow shelf sea thought to play a key role.

The spatial extent of the submerged continental shelves varies greatly. The NW European shelf sea is one of the largest and hence is likely to play a significant role in marine biogeochemical cycling, alongside providing a useful model for other systems. However, even in this relatively well studied region, there is a lack of detailed understanding of the principal controls on the cycling of carbon and the major nutrient elements, nitrogen, phosphorus and silicon. Consequently it is also difficult to predict how the cycling of these elements and hence the carbon removal they support may be altered by ongoing and potential future global change. This work package aims to address these uncertainties through a comprehensive study of the cycling of the major nutrients and carbon throughout the water column over the NW European shelf sea system.

Further details are available on the SSB website.

Participants

9 different organisations are directly involved in research for SSB Work Package 1. These institutions are

• Centre for Environment, Fisheries and Aquaculture Science (Cefas)
• National Oceanography Centre (NOC)
• Plymouth Marine Laboratory (PML)
• Scottish Association for Marine Science (SAMS) / Scottish Marine Institute (SMI)
• University of Aberdeen
• University of Bangor
• University of East Anglia (UEA)
• University of Liverpool
• University of Southampton

In addition, there are third party institutions carrying out sampling work for SSB Work Package 1, but who are not involved in the programme itself. These are:

• The Agri-Food and Biosciences Institute (AFBI)
• Irish Marine Institute (MI)
• Marine Science Scotland (MSS)

Objectives

Two overarching objectives are defined for this Work Package.

• Objective 1: Estimate the size of the continental shelf carbon pump over the whole north-west European shelf.
  This will consist of two principal activities. (1) Over a 12 month period, observations of air-sea CO₂ fluxes will be made to provide a synoptic estimate of the magnitude of carbon update by the whole shelf system. (2) Concentrations of carbon (C), nitrogen (N), phosphate (P) and silicate (Si) will be estimated in water flowing on and off the shelf. These estimates will be coupled to estimates of flow and dispersion along the shelf edge, through collaboration with the NERC Fluxes across Sloping Topography of the North East Atlantic (FASTNEt) programme to allow an observational estimate of the net off-shelf transport of C, N, P and Si.

• Objective 2: Determine the relative importance of external nutrient sources and internal biogeochemical cycling in maintaining the continental shelf pump.
  Estimates of the flux of nutrients and carbon generated in Objective 1 will be used to determine the estimation of any excess of on-shelf nutrient supply, relative to that of carbon. Work Package 1 will then quantify the processes which govern internal biogeochemical cycling by measuring the uptake ratios of N, P, Si and C into phytoplankton and the element and energy balance of organic matter production by autotrophs. Potential modifications to the relative concentrations and uptake of C, N, P and Si in the thermocline and sediment food webs will also be assessed, as will the relative importance of microbial and zooplankton turnover in controlling C, N, P and Si.

Fieldwork and data collection

Data for Objective 1 will be provided using pCO₂ systems aboard third party vessels and ferry boxes, along with measurements made through the FASTNEt programme and through the Work Package 1 process cruises detailed below. The third party cruises will be undertaken by Cefas, MI, MSS, University of Bangor and AFBI, spanning the shelf seas and shelf-edges around the United Kingdom and the Republic of Ireland.

The Work Package 1 process cruises will provide data for Objective 1 and Objective 2 and are listed in the table below. The study area is the marine shelf (and shelf-edge) of the Celtic Sea. Work will be carried out on board the NERC research vessels RRS Discovery and RRS James Cook. These cruises will focus on the physics and biogeochemistry of the benthic and pelagic zones of the water column, primarily around four main sampling sites in this area.

Activities will include Conductivity Temperature and Depth (CTD) deployments, Acoustic Doppler Current Profilers (ADCP) surveys, moorings and wire-walker deployments, autonomous gliders and submersible surveys, Marine Snow Catcher particulate matter analysis, plankton net hauls and laboratory incubations with sea water samples.

Data Activity or Cruise Information

Cruise

Complete Cruise Metadata Report is available here

Fixed Station Information

Fixed Station Information

Shelf Sea Biogeochemistry Fixed Station CANDYFLOSS/CCS

This station is one of two pelagic sites sampled on the Celtic Sea shelf as part of work package I of the Shelf Sea Biogeochemistry project. The station has a mean water depth 144 m at the following co-ordinates:

The position of this station relative to the other Shelf Sea Biogeochemistry sites can be seen from the figure below.

Sampling History

Mooring deployments

Related Fixed Station activities are detailed in Appendix 1

BODC Quality Control Flags

The following single character qualifying flags may be associated with one or more individual parameters with a data cycle:

SeaDataNet Quality Control Flags

The following single character qualifying flags may be associated with one or more individual parameters with a data cycle:

Appendix 1: Shelf Sea Biogeochemistry Fixed Station Candyfloss/CCS

Related series for this Fixed Station are presented in the table below. Further information can be found by following the appropriate links.

If you are interested in these series, please be aware we offer a multiple file download service. Should your credentials be insufficient for automatic download, the service also offers a referral to our Enquiries Officer who may be able to negotiate access.