Contributors | Affiliation | Role |
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Krause, Jeffrey W. | Dauphin Island Sea Lab (DISL) | Principal Investigator |
Maiti, Kanchan | Louisiana State University (LSU-DOCS) | Co-Principal Investigator |
Marquez Jr., Israel A. | Dauphin Island Sea Lab (DISL) | Student |
Pickering, Rebecca A. | Dauphin Island Sea Lab (DISL) | Student |
Acton, Sydney | Dauphin Island Sea Lab (DISL) | Technician |
Haskins, Christina | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
Hydrocasts were conducted at identified stations. A SeaBird CTD and rosette system, owned and maintained by Louisiana Universities Marine Consortium (LUMCON), operating institution for the R/V Pelican, was used for sampling. Calibration information can be found associated with the CTD data. Unless otherwise stated, samples used for rate measurements were collected based on the percent irradiance relative to that just below the surface.
Water was sampled from Niskin bottles and pooled into 10 L acid-cleaned carboys. For inorganic nutrients, water was filtered using 0.6 μm pore size polycarbonate membrane and immediately frozen until analysis. Filtered water was analyzed for total dissolved nitrogen (TDN), nitrate+nitrite (NO3 + NO2), nitrite, soluble reactive phosphate (SRP), and ammonium (NH4) colorimetrically using Skalar autoanalyzer (Dzwonkowski et al. 2017), and for dissolved silicic acid (Si(OH)4) using a manual colorimetric method (Krause et al. 2009). Water for Chlorophyll a was filtered through a 0.45 μm-pore 47mm diameter HAWP Millipore filter, immediately frozen, and analyzed on shore (<2 weeks) using an acetone extraction/acidification method (Lomas et al. 2019). For biogenic silica analysis, seawater was filtered through a 1.2 μm-pore polycarbonate filter (47 mm diameter) and frozen immediately. On shore, filters were dried and analyzed using a sodium-carbonate time course digestion, to correct for lithogenic silica interference, in polymethylpentene tubes (Pickering et al. in review). In 2016, NaOH digestions were also done for biogenic silica, followed by an HF digestion to quantify lithogenic silica as in Krause et al. (2009). Diatom abundance was quantified by fixing samples with Bouin's solution; in the laboratory, cells were settled in a chamber and enumerated (Utermöhl 1958).
Diatom rate processes were quantified using a radioisotope (32Si) and fluorescent dye (PDMPO) tracers. Sample bottles were incubated for 12 or 24 hours in acrylic incubators cooled with continually flowing surface water under a series of neutral density screens to simulate light levels at the depth of collection (i.e. see above). Measurement for ambient (Amb) conditions (i.e. no enrichment of Si(OH)4) and enhanced (Enh) conditions (i.e. +20 µM enrichment of Si(OH)4) were made at most stations and depths using 32Si. The gross rate of biogenic silica production was measured using the radioisotope tracer 32Si with high specific activity (>40 kBq µg Si-1) as described in Krause et al. (2011). For PDMPO uptake, dye was added to samples at ambient or enriched Si(OH)4, incubated in the same conditions as the 32Si samples, and processed as in McNair et al. (2015). The net rate of biogenic silica production was calculated from biogenic silica standing stock at the time of sampling and after a 24-hour incubation, under the same conditions as the 32Si and PDMPO, as described in Krause et al. (2010).
Data were processed in Microsoft Excel.
BCO-DMO Data Manager Processing Notes:
* added a conventional header with dataset name, PI name, version date
* modified parameter names to conform with BCO-DMO naming conventions
* blank values in this dataset are displayed as "nd" for "no data." nd is the default missing data identifier in the BCO-DMO system.
* removed all spaces in headers and replaced with underscores
* removed all units from headers
* converted dates to ISO Format yyyy-mm-dd
* merged Date_Zulu and Time_Zulu to create ISO_DateTime_UTC and then removed Zulu columns
* set Types for each data column
* merged the CLASiC 2016 and 2017 Water Column data files into one dataset
* replaced - and , in Rosette_Bottle column with ;
File |
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water_col_cat.csv (Comma Separated Values (.csv), 34.39 KB) MD5:11b88fa79c320e559dc51d1993c66b44 Primary data file for dataset ID 822048 |
Parameter | Description | Units |
Cruise | Name of specific cruise, no units | unitless |
Cast_Number | CTD Number (chronological) | unitless |
Latitude | Latitude of hydrocast | decimal degrees |
Longitude | Longitude of hydrocast | decimal degrees |
ISO_DateTime_UTC | Date/Time (UTC) ISO formatted | YYYY-MM-DDTHH:MM:SS[.xx]Z |
Date_Local | Local date of hydrocast | YYYY-MM-DD |
Time_Local | Local time of hydrocast | HH:MM |
Station_Number | specific to cruise | unitless |
Bottom_Depth | depth of water | meter (m) |
Actual_Depth | Niskin bottle sample depth | meter (m) |
Rosette_Bottle | Niskin Bottle number(s) for specific depth | unitless |
Target_pct_lo | Percent irradiance, relative to just below surface (Io), at sample depth | % lo |
Phosphate | soluble reactive phosphorus | umol/L |
Nitrate_Nitrite | dissolved nitrate plus nitrite | umol/L |
Nitrite | dissolved nitrite | umol/L |
Ammonium | dissolved ammonium | umol/L |
TDN | total dissolved nitrogen | umol/L |
Silicate | dissolved silicate | umol/L |
Pheophytin | degraded phaeopigments | ug/L |
Chlorophyll_a | chlorophyll a pigment | ug/L |
bSi | particulate biogenic silica | umol Si/L |
LSi | particulate lithogenic silica | umol Si/L |
Total_Diatom_Abundance | diatom abundance | cells/L |
Rho_Net | Average rate of net biogenic silica production | umol Si/L/d |
Rho_Net_Stdev | Standard deviation for rate of net biogenic silica production | umol Si/L/d |
Uptake_32Si_rho_Amb | 32Si-based Gross biogenic silica production at ambient silicate | umol Si/L/d |
Uptake_32Si_Vb_Amb | 32Si-based Biomass-normalized biogenic silica production at ambient silicate | d-1 |
Uptake_32Si_rho_Enh | 32Si-based Gross biogenic silica production at +20uM silicate above ambient | umol Si/L/d |
Uptake_32Si_Vb_Enh | 32Si-based Biomass-normalized biogenic silica production at +20uM silicate above ambient | d-1 |
PDMPO_Uptake_rho_Amb | PDMPO-based Gross biogenic silica production proxy at ambient silicate | nmol PDMPO/L/d |
PDMPO_Uptake_Blank_Amb | PDMPO-blank value at ambient silicate | RFU |
PDMPO_Uptake_rho_Enh | PDMPO-based Gross biogenic silica production proxy at +20uM silicate above ambient | nmol PDMPO/L/d |
PDMPO_Uptake_Blank_Enh | PDMPO-blank value at +20uM silicate above ambient | RFU |
Temperature | CTD Temperature | degrees Celsius |
Salinity | CTD Salinity, Practical | PSU |
Oxygen | CTD Oxygen sensor | mg/l |
Beam_Transmission | Beam Transmission on WET Labs C-Star | percent (%) |
Beam_Attenuation | Beam Attenuation on WET Labs C-Star | 1/m |
Fluorescence_Chl | Chlorophyll Fluorescence | ug/l |
PAR_Irradiance | Photosynthetically Active Radiation/Irradiance | uE/m2/s |
Dataset-specific Instrument Name | Trilogy fluorometer (Turner Designs) |
Generic Instrument Name | Fluorometer |
Dataset-specific Description | Quantification of Chlorophyll a and bulk PDMPO were done using a Trilogy fluorometer (Turner Designs). For Chlorophyll a, an acidification-method (acetone and HCl matrix) module was used; for PDMPO, a crude-oil module was used with a sample matrix of hydrofluoric acid and boric acid. Chlorophyll a was calibrated using a certified standard, PDMPO was calibrated using a sequential addition of stock dye purchased from the vendor. |
Generic Instrument Description | A fluorometer or fluorimeter is a device used to measure parameters of fluorescence: its intensity and wavelength distribution of emission spectrum after excitation by a certain spectrum of light. The instrument is designed to measure the amount of stimulated electromagnetic radiation produced by pulses of electromagnetic radiation emitted into a water sample or in situ. |
Dataset-specific Instrument Name | GM 25 Multicounters (Risø National Laboratory, Technical University of Denmark) |
Generic Instrument Name | GM multicounter |
Dataset-specific Description | Quantification of 32Si activity was done on a GM 25 Multicounters (Risø National Laboratory, Technical University of Denmark), each are configured to analyze five samples simultaneously. System setup includes an anti-coincidence module, which with considerable lead shielding reduces background activity to |
Generic Instrument Description | A gas flow multicounter (GM multicounter) is used for counting low-level beta doses. GM multicounters can be used for gas proportional counting of 32Si to 32P. For more information about GM multicounter usage see Krause et. al. 2011. |
Dataset-specific Instrument Name | Skalar autoanalyzer |
Generic Instrument Name | Nutrient Autoanalyzer |
Dataset-specific Description | Nutrients were analyzed colorimetrically using Skalar autoanalyzer, except for dissolved silicic acid (Si(OH)4) using a manual colorimetric method on a Genesys 10S UV-Vis spectrophotometer. Similarly, biogenic silica was digested in an alkaline solution (to solubilize particles) and analyzed as Si(OH)4 spectrophotometrically. |
Generic Instrument Description | Nutrient Autoanalyzer is a generic term used when specific type, make and model were not specified. In general, a Nutrient Autoanalyzer is an automated flow-thru system for doing nutrient analysis (nitrate, ammonium, orthophosphate, and silicate) on seawater samples. |
Website | |
Platform | R/V Pelican |
Start Date | 2017-05-03 |
End Date | 2017-05-13 |
Description | More information about this cruise can be found in R2R: https://www.rvdata.us/search/cruise/PE17-20 |
Website | |
Platform | R/V Pelican |
Start Date | 2016-08-26 |
End Date | 2016-09-06 |
NSF Award Abstract:
The Louisiana Shelf system in the northern Gulf of Mexico is fed by the Mississippi River and its many tributaries which contribute large quantities of nutrients from agricultural fertilizer to the region. Input of these nutrients, especially nitrogen, has led to eutrophication. Eutrophication is the process wherein a body of water such as the Louisiana Shelf becomes enriched in dissolved nutrients that increase phytoplankton growth which eventually leads to decreased oxygen levels in bottom waters. This has certainly been observed in this area, and diatoms, a phytoplankton which represents the base of the food chain, have shown variable silicon/nitrogen (Si/N) ratios. Because diatoms create their shells from silicon, their growth is controlled not only by nitrogen inputs but the availability of silicon. Lower Si/N ratios are showing that silicon may be playing an increasingly important role in regulating diatom production in the system. For this reason, a scientist from the University of South Alabama will determine the biogeochemical processes controlling changes in Si/N ratios in the Louisiana Shelf system. One graduate student on their way to a doctorate degree and three undergraduate students will be supported and trained as part of this project. Also, four scholarships for low-income, high school students from Title 1 schools will get to participate in a month-long summer Marine Science course at the Dauphin Island Sea Laboratory and be included in the research project. The study has significant societal benefits given this is an area where $2.4 trillion gross domestic product revenue is tied up in coastal resources. Since diatoms are at the base of the food chain that is the biotic control on said coastal resources, the growth of diatoms in response to eutrophication is important to study.
Eutrophication of the Mississippi River and its tributaries has the potential to alter the biological landscape of the Louisiana Shelf system in the northern Gulf of Mexico by influencing the Si/N ratios below those that are optimal for diatom growth. A scientist from the University of South Alabama believes the observed changes in the Si/N ratio may indicate silicon now plays an important role in regulating diatom production in the system. As such, understanding the biotic and abiotic processes controlling the silicon cycle is crucial because diatoms dominate at the base of the food chain in this highly productive region. The study will focus on following issues: (1) the importance of recycled silicon sources on diatom production; (2) can heavily-silicified diatoms adapt to changing Si/N ratios more effectively than lightly-silicified diatoms; and (3) the role of reverse weathering in sequestering silicon thereby reducing diffusive pore-water transport. To attain these goals, a new analytical approach, the PDMPO method (compound 2-(4-pyridyl)-5-((4-(2-dimethylaminoethylamino-carbamoyl)methoxy)phenyl)oxazole) that quantitatively measures taxa-specific silica production would be used.
Funding Source | Award |
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NSF Division of Ocean Sciences (NSF OCE) |