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bacteria

Data Object bacteria
contact PIs:
name        title
Jacques L. Oliver         Principal Investigator

Dataset description

Bacterial Abundance and Production from bottle samples

Acquisition description

 dates:           24 January 2002 to 21 February 2002  (20020124-20020221) 
 location:        N: -52.56100  S: -66.61150  W: -172.69267  E: -166.94733 


15 August 2008: Prepared for OCB data system by Cyndy Chandler, OCB DMO (WHOI) from documentation contributed by Jacques Olivier, Helen Quinby, Robert Daniels, and Hugh Ducklow

Original Excel file contributed: 8 November, 2002
and downloaded from MBARI by OCB DMO:
copy of original Excel file

Contact: Jacques Oliver (Email: jloliver@vims.edu)

R/V Melville Bacterial Measurements Methodology

Bacterial Abundance Flow cytometry (FCM)

1. 9.5 ml sample from CTD or TM rosette, fixed to final concentration of 1% formaldehyde
2. Sample frozen at -80 C
3. On land, triplicate samples were analyzed using a Beckman-Coulter Epics Altra equipped with an Enterprise II laser at 488 nm using 190mV (intra-sample variation).
4. About 100 ml of sample were measured following Troussellier et al. (1999) with addition of 2.5 mM SYTO 13 and a 10 minute incubation.
5. This analysis was done on triplicate 1.0 ml samples to which 1.0 mm beads (Molecular Probes, Fluo Spheres, F-8888) were also added at a 10E6/ml concentration.

The beads determined flow rate and uniformity in fluorescence signal. Discrimination was done on a positive green fluorescence and the plot was green fluorescence (devoid of any red fluorescence) against side scatter. Analytical variation was 3%.

Reference: Troussellier, M., C. Courties, P. Lebaron, and P.Servais. 1999. FEMS Microbiology Ecology 29: 319-330.


Bacterial Abundance Acridine orange direct counts (AODC)

  1. 10-15 ml sample fixed to final concentration of 1% formaldehyde               		
  2. Sample filtered onto 0.2 micron blackened polycarbonate filter               		
  3. Filter stained with 45% (w/v) acridine orange                		
  4. Filter mounted onto glass slide with immersion oil and coverslip               		
  5. Bacteria enumerated via epifluorescence microscopy               		
  6. Intra-sample variation reported               		

Reference: Kirchman, D., Sigda, J., Kapuscinski, R., and Mitchell, R. 1982. Appl. Envrion. Microbiol. 44:376-382


Bacterial Production Thymidine (TdR) and Leucine (Leu) Incorporation

   1. 1.6 ml sample spiked with tritiated thymidine or tritiated leucine               		
   2. Samples run in triplicate with one negative control containing 6% trichloroacetic acid (TCA)               		
   3. Samples incubated at in situ temperatures in the dark for 8-20 hours (depending on water temp)               		
   4. Incubation stopped by adding TCA (6% final conc.) to each sample               		
   5. Nucleic acid extracted with TCA and ethanol               		
   6. 1.6 ml Ultima Gold scintillation cocktail added               		
   7. 3 minute counts on each sample on scintillation counter 

Reference: Smith, D.C. and Azam, F. 1992. Mar. Microb. Food Webs. 6:107-114.

Processing description

 Change history:
    070509: downloaded original data (SOFeX_melville_Bacterial_Data.xls) from SOFeX project data web site.
            data prepared database by Dave DuBois (OCB DMO, WHOI) 
    080815: added to OCB database by Cyndy Chandler, OCB DMO, (cchandler@whoi.edu)
  
 OCB DMO Note: Four worksheets were contained in the original file: Methods, North Patch, 
    South Patch, and Transects. The Methods worksheet was extracted to file 
    Methods_Melville_Bact_Abund_Prod.xls. The other three worksheets were combined into one 
    and were sorted by date. The Latitude value for Transect 3, Station 42 was changed from 
    6 07.06 S to 66 07.06 S before converting all Lat and Lon values to decimal degrees.
    Two bottle cast entries were included for USCG Polar Star on 16-Feb in the original file 
    and are retained here with data collected during the Melville cruise.

 PI note: Date = Local Day (Kiwi). Event # = Julian Day, UTC. 
    North Patch Summary: 2 IN, 2 OUT. 
    South Patch Summary: 7 IN, 4 OUT (R/V Melville); 1 IN, 1 OUT (USCG Polar Star). 
    Transect Summary: 3 transects.


Field Names List

ParameterDescriptionUnits
eventunique sampling event number from event log (day of year and time (UTC))doYhhmm
date_LNZ local daydimensionless
day_SSouth patch local date days since start of first fertilization, day zero=24-Jan ??integer days
lonlongitude; negative denotes Westdecimal degrees
latlatitude; negative denotes Southdecimal degrees
patch_locsampling location relative to patch see explanation in cruise event log), T = transectdimensionless
stationstation location numberdimensionless
ev_typeevent type descriptor stringdimensionless
botNiskin bottle numberdimensionless
depthdepth, calculted from pressure??meters
light_levlight levelpercent
bact_cytbacterial abundance, Flow Cytometry (FCM)cells/liter
bact_aodcbacterial abundance, Acridine Orange Direct Count (AODC)cells/liter
thy_incorpThymidine (TdR) incorporation ratepicomoles/liter/hour
thy_sdstandard deviation of thymidine incorporation ratepicomoles/liter/hour
leuc_incorpLeucine incorporation ratepicomoles/liter/hour
leuc_sdstandard deviation of leucine incorporation ratepicomoles/liter/hour

Platforms List

R/V Melville COOK19MV

Instruments List

  1. Niskin:

  2. Trace Metal Bottle:


This document is created from the content of the BCO-DMO metadata database.    2009-11-22  09:17:52

info app: /home/ocb/dbase v.090827 CLC
Data URL: http://ocb.whoi.edu/jg/serv/OCB/SOFeX/Melville/bacteria.