Contributors | Affiliation | Role |
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Pinckney, James L. | University of South Carolina at Columbia | Principal Investigator |
Ake, Hannah | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
Detection limits of the results of HPLC – derived photopigment concentrations for bioassays.
These are the detection limits for this dataset: HPLC Photopigment Data for Bioassays
Methodology from Pickney, J.L.: The USC HPLC Method - Technical Description.pdf
BCO-DMO Data Processing Notes:
-Reformatted column names to comply with BCO-DMO standards.
-Data were originally separated by month (September and November) into two spreadsheets. Data were combined into one file and the columns "month" and "year" were added.
-Colors and headers were removed.
File |
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detection_limits.csv (Comma Separated Values (.csv), 23.35 KB) MD5:9b6c2216d2fc8ea2661d458e8c5e54f2 Primary data file for dataset ID 710183 |
Parameter | Description | Units |
Year | Year sample was taken; YYYY | unitless |
Month | Month sample was taken | unitless |
Sample_Number | Sample number | unitless |
Chl_LOD | Chlorophyll c1+c2 effective limit of detection | micrograms per liter |
Chl_LOQ | Chlorophyll c1+c2 effective limit of quantification | micrograms per liter |
Perid_LOD | Peridinin effective limit of detection | micrograms per liter |
Perid_LOQ | Peridinin effective limit of quanitification | micrograms per liter |
ButFuc19_LOD | 19' Butanoyloxyfucoxanthin effective limit of detection | micrograms per liter |
ButFuc19_LOQ | 19' Butanoyloxyfucoxanthin effective limit of quantification | micrograms per liter |
Fuco_LOD | Fucoxanthin effective limit of detection | micrograms per liter |
Fuco_LOQ | Fucoxanthin effective limit of quantification | micrograms per liter |
HexFuc19_LOD | 19' Hexanoyloxyfucoxathin effective limit of detection | micrograms per liter |
HexFuc19_LOQ | 19' Hexanoyloxyfucoxathin effective limit of quantification | micrograms per liter |
Neo_LOD | Neoxanthin effective limit of detection | micrograms per liter |
Neo_LOQ | Neoxanthin effective limit of quantification | micrograms per liter |
Viola_LOD | Violaxanthin effective limit of detection | micrograms per liter |
Viola_LOQ | Violaxanthin effective limit of quantification | micrograms per liter |
Diad_LOD | Diatoxanthin effective limit of detection | micrograms per liter |
Diad_LOQ | Diatoxanthin effective limit of quantification | micrograms per liter |
Allox_LOD | Alloxanthin effective limit of detection | micrograms per liter |
Allox_LOQ | Alloxanthin effective limit of quantification | micrograms per liter |
Diat_LOD | Diatoxanthin effective limit of detection | micrograms per liter |
Diat_LOQ | Diatoxanthin effective limit of quantification | micrograms per liter |
Lutein_LOD | Lutein effective limit of detection | micrograms per liter |
Lutein_LOQ | Lutein effective limit of quantification | micrograms per liter |
Zeax_LOD | Zeaxanthin effective limit of detection | micrograms per liter |
Zeax_LOQ | Zeaxanthin effective limit of quantification | micrograms per liter |
Gyro_LOD | Gyroxanthin effective limit of detection | micrograms per liter |
Gyro_LOQ | Gyroxanthin effective limit of quantification | micrograms per liter |
Chl_b_LOD | Chlorophyll b effective limit of detection | micrograms per liter |
Chl_b_LOQ | Chlorophyll b effective limit of quantification | micrograms per liter |
Chl_a_LOD | Chlorophyll a effective limit of detection | micrograms per liter |
Chl_a_LOQ | Chlorophyll a effective limit of quantification | micrograms per liter |
Dataset-specific Instrument Name | Temperature-controlled autosampler (Shimadzu SIL10-A vp) with a 500 µl injection loop |
Generic Instrument Name | High-Performance Liquid Chromatograph |
Dataset-specific Description | Used in HPLC Analysis |
Generic Instrument Description | A High-performance liquid chromatograph (HPLC) is a type of liquid chromatography used to separate compounds that are dissolved in solution. HPLC instruments consist of a reservoir of the mobile phase, a pump, an injector, a separation column, and a detector. Compounds are separated by high pressure pumping of the sample mixture onto a column packed with microspheres coated with the stationary phase. The different components in the mixture pass through the column at different rates due to differences in their partitioning behavior between the mobile liquid phase and the stationary phase. |
Dataset-specific Instrument Name | Photodiode array detector (PDA, Shimadzu SPD-M10A vp; 200 to 800 nm range) |
Generic Instrument Name | High-Performance Liquid Chromatograph |
Dataset-specific Description | Used in HPLC analysis |
Generic Instrument Description | A High-performance liquid chromatograph (HPLC) is a type of liquid chromatography used to separate compounds that are dissolved in solution. HPLC instruments consist of a reservoir of the mobile phase, a pump, an injector, a separation column, and a detector. Compounds are separated by high pressure pumping of the sample mixture onto a column packed with microspheres coated with the stationary phase. The different components in the mixture pass through the column at different rates due to differences in their partitioning behavior between the mobile liquid phase and the stationary phase. |
Dataset-specific Instrument Name | Flow Scintillation Counter (Packard Radiomatic 525a, 500 ul counting cell) |
Generic Instrument Name | Liquid Scintillation Counter |
Dataset-specific Description | Used to measure chl a |
Generic Instrument Description | Liquid scintillation counting is an analytical technique which is defined by the incorporation of the radiolabeled analyte into uniform distribution with a liquid chemical medium capable of converting the kinetic energy of nuclear emissions into light energy. Although the liquid scintillation counter is a sophisticated laboratory counting system used the quantify the activity of particulate emitting (ß and a) radioactive samples, it can also detect the auger electrons emitted from 51Cr and 125I samples. |
Dataset-specific Instrument Name | Binary Gradient Pump (Shimadzu dual LC10-AT vp and Controller SCL-10A vp) |
Generic Instrument Name | Pump |
Dataset-specific Description | Used in HPLC analysis |
Generic Instrument Description | A pump is a device that moves fluids (liquids or gases), or sometimes slurries, by mechanical action. Pumps can be classified into three major groups according to the method they use to move the fluid: direct lift, displacement, and gravity pumps |
Phytoplankton, traditionally viewed as primary producers at the base of aquatic food webs, provide an energy source for higher trophic levels. However, some phytoplankton species function as both primary producers and heterotrophic secondary consumers. Phytoplankton that are photosynthetically competent but also take up and assimilate organic compounds are classified as facultative mixotrophs or, more simply, photomixotrophs. Unfortunately, we currently have few estimates of the proportion of the phytoplankton community that function as photomixotrophs, their rate of secondary production, or their temporal variation in abundance. Current paradigms about trophodynamics in marine systems do not consider this potentially important alternative pathway for energy flow for phytoplankton. The implication is that we may be missing a significant, fundamental process that affects carbon cycling and trophodynamics in estuarine systems. Furthermore, changes in the DOC composition due to anthropogenic alterations may result in changes in phytoplankton community structure and possibly promote the proliferation of harmful algal bloom species. In terms of ecosystem function, even moderate rates of photomixotrophy could potentially alter our current understanding of phytoplankton productivity, overall C turnover, competitive interactions, and energy transfer in estuarine environments. This project will use a novel approach to provide quantitative measures of the in situ rates and magnitudes of facultative heterotrophy in natural, estuarine phytoplankton communities over seasonal time scales in a representative estuarine ecosystem. The project will utilize a unique 14C radiolabeling technique to quantify the in situ assimilation rates of DOC by estuarine photomixotrophs and estimate the amount of DOC converted to phytoplankton biomass by photomixotrophy over seasonal time scales. This information will provide new insights into carbon dynamics in estuaries, the contribution of DOC to estuarine food webs, and the importance of photomixotrophy in determining the structural and functional characteristics of estuarine phytoplankton communities.
Funding Source | Award |
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NSF Division of Ocean Sciences (NSF OCE) |