Algal pigment concentrations measured by HPLC from RVIB Nathaniel B. Palmer cruise in the Ross Sea, Southern Ocean from 2017-2018.

Website: https://www.bco-dmo.org/dataset/778881
Data Type: Cruise Results
Version: 1
Version Date: 2019-10-09

Project
» Collaborative Research: Cobalamin and Iron Co-Limitation Of Phytoplankton Species in Terra Nova Bay (CICLOPS)
ContributorsAffiliationRole
DiTullio, GiacomoCollege of Charleston (CofC)Principal Investigator
Lee, PeterCollege of Charleston (CofC)Co-Principal Investigator
Soenen, KarenWoods Hole Oceanographic Institution (WHOI BCO-DMO)BCO-DMO Data Manager

Abstract
Algal pigment concentrations as measured by HPLC from RVIB Nathaniel B. Palmer cruise in the Ross Sea, Southern Ocean from 2017-2018.


Coverage

Spatial Extent: N:-72.44818 E:-116.9882 S:-78.6294 W:167.5528
Temporal Extent: 2017-12-31 - 2018-02-19

Dataset Description

Algal pigment concentrations as measured by HPLC from RVIB Nathaniel B. Palmer cruise in the Ross Sea, Southern Ocean from 2017-2018.


Acquisition Description

Algal HPLC samples were collected by gentile filtration under low vacuum through GF/F filters and frozen at -80C for on-shore analysis. Samples were extracted in acetone and analyzed using an Agilent 1100 HPLC system equipped with autosampler, photodiode array and fluorescence detectors. The gradient elution program utilized was a slight modification of the Zapata et al. method (2000). Complete details of the HPLC method are described elsewhere (DiTullio and Geesey 2002).

High Performance Liquid Chromatograph (HPLC) Agilent 1100 equipped with autosampler, photodiode array and fluorescence detectors

 


Processing Description

Pigment concentrations were determined using standard peak integration procedures with Agilent’s ChemStation (version B.03.02), and entered into Microsoft Excel Spreadsheets for submission to BCO-DMO. Parameters reported were: chlorophyll c3, chlorophyllide, magnesium-2,4-divinyl phaeoporphyrin a5 monomethyl ester, chlorophyll c2, chlorophyll c1, peridinin, pheophorbide a, 19-prime butanoyloxyfucoxanthin, fucoxanthin, neoxanthin, prasinoxanthin, violaxanthin, 19-prime hexanoyloxyfucoxanthin, diadinoxanthin, cis-fucoxanthin, alloxanthin, diatoxanthin, monadoxanthin, zeaxanthin, lutein, crocoxanthin, chlorophyll b, divinyl chlorophyll a, chlorophyll a, pheophytin a, carotene-alpha and carotene-beta.

BCO-DMO processing notes:

  • Adjusted column names
  • Adjusted date format to yyyy-mm-dd for increased interoperability

 


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Related Publications

DiTullio, G. R., and M. E. Geesey (2002), Photosynthetic pigments in marine algae and bacteria, in The Encyclopedia of Environmental Microbiology, edited by G. Bitton, pp. 2453– 2470, John Wiley, Hoboken, N. J.
Zapata, M., Rodríguez, F., & Garrido, J. (2000). Separation of chlorophylls and carotenoids from marine phytoplankton:a new HPLC method using a reversed phase C8 column and pyridine-containing mobile phases. Marine Ecology Progress Series, 195, 29–45. doi:10.3354/meps195029

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Parameters

ParameterDescriptionUnits
DateDate (UTC) - format: yyyy-mm-dd unitless
StationStation Identifier unitless
LatitudeLatitude (South is negative) decimal degrees
LongitudeLongitude (West is negative) decimal degrees
DepthSample depth meters (m)
NiskinNiskin Bottle Number unitless
SampleSample Number unitless
Fltr_VolVolume Filtered liter (L)
Chl_C3Chlorophyll c3 nanogram per liter (ng/L)
Chl_lideChlorophyllide nanogram per liter (ng/L)
MgDVPMagnesium-2;4-divinyl nanogram per liter (ng/L)
Chl_C2Chlorophyll c2 nanogram per liter (ng/L)
Chl_C1Chlorophyll c1 nanogram per liter (ng/L)
PeridininPeridinin nanogram per liter (ng/L)
Ph_idePheophorbide a nanogram per liter (ng/L)
But_1919'-butanoyloxyfucoxanthin nanogram per liter (ng/L)
FucoFucoxanthin nanogram per liter (ng/L)
NeoNeoxanthin nanogram per liter (ng/L)
PrasinoPrasinoxanthin nanogram per liter (ng/L)
ViolaViolaxanthin nanogram per liter (ng/L)
Hex_1919'-hexanoyloxyfucoxanthin nanogram per liter (ng/L)
DiadinoDiadinoxanthin nanogram per liter (ng/L)
cis_fucocis-Fucoxanthin nanogram per liter (ng/L)
AlloAlloxanthin nanogram per liter (ng/L)
DiatoDiatoxanthin nanogram per liter (ng/L)
MonadMonadoxanthin nanogram per liter (ng/L)
ZeaZeaxanthin nanogram per liter (ng/L)
LuteinLutein nanogram per liter (ng/L)
CrocoCrocoxanthin nanogram per liter (ng/L)
Chl_bChlorophyll b nanogram per liter (ng/L)
Chl_a_allomerChlorophyll a allomer nanogram per liter (ng/L)
Chl_C2_MGDGChlorophyll c2 MGDG nanogram per liter (ng/L)
DV_Chl_aDivinyl chlorophyll a nanogram per liter (ng/L)
Chl_aChlorophyll a nanogram per liter (ng/L)
Ph_tinPhaeophytin a nanogram per liter (ng/L)
a_CarAlpha-carotene nanogram per liter (ng/L)
b_CarBeta-carotene nanogram per liter (ng/L)


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Instruments

Dataset-specific Instrument Name
Agilent 1100
Generic Instrument Name
High Performance Liquid Chromatograph
Dataset-specific Description
High Performance Liquid Chromatograph (HPLC) Agilent 1100 equipped with autosampler, photodiode array and fluorescence detectors.  
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. (http://www.files.chem.vt.edu/chem-ed/sep/lc/hplc.html)


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Deployments

NBP1801

Website
Platform
RVIB Nathaniel B. Palmer
Start Date
2017-12-16
End Date
2018-03-03
Description
Chief Scientist: Saba, Grace Start Port: Punta Arenas End Port: Hobart


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Project Information

Collaborative Research: Cobalamin and Iron Co-Limitation Of Phytoplankton Species in Terra Nova Bay (CICLOPS)

Coverage: Amundsen Sea, Ross Sea, Terra Nova Bay


NSF abstract: Phytoplankton blooms in the coastal waters of the Ross Sea, Antarctica are typically dominated by either diatoms or Phaeocystis Antarctica (a flagellated algae that often can form large colonies in a gelatinous matrix). The project seeks to determine if an association of bacterial populations with Phaeocystis antarctica colonies can directly supply Phaeocystis with Vitamin B12, which can be an important co-limiting micronutrient in the Ross Sea. The supply of an essential vitamin coupled with the ability to grow at lower iron concentrations may put Phaeocystis at a competitive advantage over diatoms. Because Phaeocystis cells can fix more carbon than diatoms and Phaeocystis are not grazed as efficiently as diatoms, the project will help in refining understanding of carbon dynamics in the region as well as the basis of the food web webs. Such understanding also has the potential to help refine predictive ecological models for the region. The project will conduct public outreach activities and will contribute to undergraduate and graduate research. Engagement of underrepresented students will occur during summer student internships. A collaboration with Italian Antarctic researchers, who have been studying the Terra Nova Bay ecosystem since the 1980s, aims to enhance the project and promote international scientific collaborations. The study will test whether a mutualistic symbioses between attached bacteria and Phaeocystis provides colonial cells a mechanism for alleviating chronic Vitamin B12 co-limitation effects thereby conferring them with a competitive advantage over diatom communities. The use of drifters in a time series study will provide the opportunity to track in both space and time a developing algal bloom in Terra Nova Bay and to determine community structure and the physiological nutrient status of microbial populations. A combination of flow cytometry, proteomics, metatranscriptomics, radioisotopic and stable isotopic labeling experiments will determine carbon and nutrient uptake rates and the role of bacteria in mitigating potential vitamin B12 and iron limitation. Membrane inlet and proton transfer reaction mass spectrometry will also be used to estimate net community production and release of volatile organic carbon compounds that are climatically active. Understanding how environmental parameters can influence microbial community dynamics in Antarctic coastal waters will advance an understanding of how changes in ocean stratification and chemistry could impact the biogeochemistry and food web dynamics of Southern Ocean ecosystems.


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Funding

Funding SourceAward
NSF Office of Polar Programs (formerly NSF PLR) (NSF OPP)

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