Ice core bacteria data from RVIB Nathaniel B. Palmerand ARSV Laurence M. Gould cruises NBP0104, LMG0106, NBP0204,and LMG0205 in the Southern Ocean from 2001-2002 (SOGLOBEC project; Sea Ice Microbes project)

<h2>Bacteria Abundance, Biomass and Chlorophyll <em>a</em> in Ice Cores</h2> <p><strong>NOTES:</strong><br /> NBP0104: Cores labelled with \"DNA\" were collected for DNA analysis.</p> <pre> <strong>Contributor:</strong>...

Full description

Bibliographic Details
Main Author: Chris H. Fritsen
Format: Dataset
Language:unknown
Published: Biological and Chemical Oceanography Data Management Office (BCO-DMO) 2003
Subjects:
Online Access:https://search.dataone.org/view/sha256:32e26d60aa59e343cbc4db12adb42e6e6828d045014728f42143820116efbbc6
id dataone:sha256:32e26d60aa59e343cbc4db12adb42e6e6828d045014728f42143820116efbbc6
record_format openpolar
institution Open Polar
collection Biological and Chemical Oceanography Data Management Office (BCO-DMO) (via DataONE)
op_collection_id dataone:urn:node:BCODMO
language unknown
topic oceans
spellingShingle oceans
Chris H. Fritsen
Ice core bacteria data from RVIB Nathaniel B. Palmerand ARSV Laurence M. Gould cruises NBP0104, LMG0106, NBP0204,and LMG0205 in the Southern Ocean from 2001-2002 (SOGLOBEC project; Sea Ice Microbes project)
topic_facet oceans
description <h2>Bacteria Abundance, Biomass and Chlorophyll <em>a</em> in Ice Cores</h2> <p><strong>NOTES:</strong><br /> NBP0104: Cores labelled with \"DNA\" were collected for DNA analysis.</p> <pre> <strong>Contributor:</strong> Dr. Christian Fritsen University and Community College System of Nevada Desert Research Institute Div. of Earth and Ecosystem Sciences 2215 Raggio Parkway Reno, NV 89512 Office: 775/673-7487 </pre> <h3>BG 235 - Methods used for chlorophyll <em>a</em> (chla) analysis and bacteria biomass determination</h3> <p><strong>Core Sampling techniques:</strong></p> <p>Sampling methods for recovery of chlorophyll <em>a</em> and bacteria from sea ice cores follows those described in:<br /> Garrison, D.L. and K.R. Buck(1986), Organism losses during ice melting: a serious bias in sea ice community studies. <em>Polar Biol.</em>, <strong>6</strong>:237-239.</p> <p>Recommendations for reporting were used as outlined by:<br /> Horner, R. <em>et al.</em>,(1992), Ecology of Sea Ice Biota. I: Habitat, Terminology and Methodology. <em> Polar Biol.</em> <strong>12</strong>:417-427</p> <p><strong>Analytic Techniques:</strong></p> <p>Chla (mg m<sup>-3</sup>):</p> <ul> <li>determined fluorometrically (Turner Designs 10AU Fluorometer) following extraction in 90% acetone (Parsons <em>et al</em>., 1984)</li> <li>ice core chla corrected to account for chla in filtered sea water (FSW) added to core sections during melting</li> </ul> <p>Bacteria cell abundance (cells m<sup>-3</sup>) and biomass (mg C m<sup>-3</sup>):</p> <p>LMG 0106</p> <ul> <li>preserved (0.5% glutaraldehyde) samples stained with 4',6-diamidino-2-phenylindole (DAPI; 0.1 to 0.3% final concentration), filtered through 0.2 mm black, polycarbonate membrane filters, and mounted onto glass microscope slides on the ship (within 24 hours following collection)</li> <li>bacteria enumerated using epifluorescence microscopy and sized using digital images taken with Image Pro Plus</li> <li>bacteria biomass determined using cell abundance, cell biovolume (BV; mm<sup>3</sup>; as determined from mean length and width measurements), and an allometric conversion factor for bacterial carbon per volume specific for DAPI-stained bacteria (cellular carbon = 218 X BV<sup>0.86</sup>; Loferer-Kribacher <em>et al.</em>, 1998).</li> <li>ice core samples corrected for FSW dilution</li> </ul> <p>NBP 0104</p> <ul> <li>preserved (0.5% glutaraldehyde) samples stained with Sybri Gold (0.01% final concentration), filtered through 0.2 mm Anodisc filters (Whatman), and mounted onto glass microscope slides at home institution (~1-2 months following collection)</li> <li>bacteria enumerated using epifluorescence microscopy and sized using digital images taken with Image Pro Plus</li> <li>bacteria biomass determined using cell abundance, cell biovolume (BV; mm<sup>3</sup>), and an allometric conversion factor for bacterial carbon per volume specific for Acridine Orange-stained bacteria (cellular carbon = 89.9 X BV<sup>0.59</sup>; Simon and Azam, 1989). Note: an AO-specific carbon per volume conversion factor was used in calculating biomass in Sybri Gold-stained samples because both AO and Sybri Gold stain bacteria cells similarly relative to DAPI (unpublished data).</li> <li>ice core samples corrected for FSW dilution</li> </ul> <p>Loferer-Kribacher, M., Klima, J., and R. Psenner. 1998. Determination of bacterial cell dry mass by transmission electron microscopy and densitometric image analysis. Applied and Environmental Microbiology. 64:688-694.</p> <p>Parsons,T.R., Maita, Y., and C.M. Lalli. 1984. A manual of chemical and biological methods for seawater analysis. Pergamon Press. Elmsford, New York.</p> <p>Simon, M., and F. Azam. 1989. Protein content and protein synthesis rates of planktonic marine bacteria. Marine Ecology Progress Series. 51, 201-213.</p> <p><em>updated: April 20, 2006</em></p>
format Dataset
author Chris H. Fritsen
author_facet Chris H. Fritsen
author_sort Chris H. Fritsen
title Ice core bacteria data from RVIB Nathaniel B. Palmerand ARSV Laurence M. Gould cruises NBP0104, LMG0106, NBP0204,and LMG0205 in the Southern Ocean from 2001-2002 (SOGLOBEC project; Sea Ice Microbes project)
title_short Ice core bacteria data from RVIB Nathaniel B. Palmerand ARSV Laurence M. Gould cruises NBP0104, LMG0106, NBP0204,and LMG0205 in the Southern Ocean from 2001-2002 (SOGLOBEC project; Sea Ice Microbes project)
title_full Ice core bacteria data from RVIB Nathaniel B. Palmerand ARSV Laurence M. Gould cruises NBP0104, LMG0106, NBP0204,and LMG0205 in the Southern Ocean from 2001-2002 (SOGLOBEC project; Sea Ice Microbes project)
title_fullStr Ice core bacteria data from RVIB Nathaniel B. Palmerand ARSV Laurence M. Gould cruises NBP0104, LMG0106, NBP0204,and LMG0205 in the Southern Ocean from 2001-2002 (SOGLOBEC project; Sea Ice Microbes project)
title_full_unstemmed Ice core bacteria data from RVIB Nathaniel B. Palmerand ARSV Laurence M. Gould cruises NBP0104, LMG0106, NBP0204,and LMG0205 in the Southern Ocean from 2001-2002 (SOGLOBEC project; Sea Ice Microbes project)
title_sort ice core bacteria data from rvib nathaniel b. palmerand arsv laurence m. gould cruises nbp0104, lmg0106, nbp0204,and lmg0205 in the southern ocean from 2001-2002 (soglobec project; sea ice microbes project)
publisher Biological and Chemical Oceanography Data Management Office (BCO-DMO)
publishDate 2003
url https://search.dataone.org/view/sha256:32e26d60aa59e343cbc4db12adb42e6e6828d045014728f42143820116efbbc6
op_coverage ENVELOPE(-76.781,-65.61,-65.62,-69.25)
BEGINDATE: 2001-07-28T00:00:00Z ENDDATE: 2002-09-07T00:00:00Z
long_lat ENVELOPE(-58.700,-58.700,-63.817,-63.817)
ENVELOPE(-76.781,-65.61,-65.62,-69.25)
geographic Southern Ocean
Reno
geographic_facet Southern Ocean
Reno
genre ice core
Sea ice
Southern Ocean
genre_facet ice core
Sea ice
Southern Ocean
_version_ 1800873324965789696
spelling dataone:sha256:32e26d60aa59e343cbc4db12adb42e6e6828d045014728f42143820116efbbc6 2024-06-03T18:46:56+00:00 Ice core bacteria data from RVIB Nathaniel B. Palmerand ARSV Laurence M. Gould cruises NBP0104, LMG0106, NBP0204,and LMG0205 in the Southern Ocean from 2001-2002 (SOGLOBEC project; Sea Ice Microbes project) Chris H. Fritsen ENVELOPE(-76.781,-65.61,-65.62,-69.25) BEGINDATE: 2001-07-28T00:00:00Z ENDDATE: 2002-09-07T00:00:00Z 2003-12-03T00:00:00Z https://search.dataone.org/view/sha256:32e26d60aa59e343cbc4db12adb42e6e6828d045014728f42143820116efbbc6 unknown Biological and Chemical Oceanography Data Management Office (BCO-DMO) oceans Dataset 2003 dataone:urn:node:BCODMO 2024-06-03T18:19:46Z <h2>Bacteria Abundance, Biomass and Chlorophyll <em>a</em> in Ice Cores</h2> <p><strong>NOTES:</strong><br /> NBP0104: Cores labelled with \"DNA\" were collected for DNA analysis.</p> <pre> <strong>Contributor:</strong> Dr. Christian Fritsen University and Community College System of Nevada Desert Research Institute Div. of Earth and Ecosystem Sciences 2215 Raggio Parkway Reno, NV 89512 Office: 775/673-7487 </pre> <h3>BG 235 - Methods used for chlorophyll <em>a</em> (chla) analysis and bacteria biomass determination</h3> <p><strong>Core Sampling techniques:</strong></p> <p>Sampling methods for recovery of chlorophyll <em>a</em> and bacteria from sea ice cores follows those described in:<br /> Garrison, D.L. and K.R. Buck(1986), Organism losses during ice melting: a serious bias in sea ice community studies. <em>Polar Biol.</em>, <strong>6</strong>:237-239.</p> <p>Recommendations for reporting were used as outlined by:<br /> Horner, R. <em>et al.</em>,(1992), Ecology of Sea Ice Biota. I: Habitat, Terminology and Methodology. <em> Polar Biol.</em> <strong>12</strong>:417-427</p> <p><strong>Analytic Techniques:</strong></p> <p>Chla (mg m<sup>-3</sup>):</p> <ul> <li>determined fluorometrically (Turner Designs 10AU Fluorometer) following extraction in 90% acetone (Parsons <em>et al</em>., 1984)</li> <li>ice core chla corrected to account for chla in filtered sea water (FSW) added to core sections during melting</li> </ul> <p>Bacteria cell abundance (cells m<sup>-3</sup>) and biomass (mg C m<sup>-3</sup>):</p> <p>LMG 0106</p> <ul> <li>preserved (0.5% glutaraldehyde) samples stained with 4',6-diamidino-2-phenylindole (DAPI; 0.1 to 0.3% final concentration), filtered through 0.2 mm black, polycarbonate membrane filters, and mounted onto glass microscope slides on the ship (within 24 hours following collection)</li> <li>bacteria enumerated using epifluorescence microscopy and sized using digital images taken with Image Pro Plus</li> <li>bacteria biomass determined using cell abundance, cell biovolume (BV; mm<sup>3</sup>; as determined from mean length and width measurements), and an allometric conversion factor for bacterial carbon per volume specific for DAPI-stained bacteria (cellular carbon = 218 X BV<sup>0.86</sup>; Loferer-Kribacher <em>et al.</em>, 1998).</li> <li>ice core samples corrected for FSW dilution</li> </ul> <p>NBP 0104</p> <ul> <li>preserved (0.5% glutaraldehyde) samples stained with Sybri Gold (0.01% final concentration), filtered through 0.2 mm Anodisc filters (Whatman), and mounted onto glass microscope slides at home institution (~1-2 months following collection)</li> <li>bacteria enumerated using epifluorescence microscopy and sized using digital images taken with Image Pro Plus</li> <li>bacteria biomass determined using cell abundance, cell biovolume (BV; mm<sup>3</sup>), and an allometric conversion factor for bacterial carbon per volume specific for Acridine Orange-stained bacteria (cellular carbon = 89.9 X BV<sup>0.59</sup>; Simon and Azam, 1989). Note: an AO-specific carbon per volume conversion factor was used in calculating biomass in Sybri Gold-stained samples because both AO and Sybri Gold stain bacteria cells similarly relative to DAPI (unpublished data).</li> <li>ice core samples corrected for FSW dilution</li> </ul> <p>Loferer-Kribacher, M., Klima, J., and R. Psenner. 1998. Determination of bacterial cell dry mass by transmission electron microscopy and densitometric image analysis. Applied and Environmental Microbiology. 64:688-694.</p> <p>Parsons,T.R., Maita, Y., and C.M. Lalli. 1984. A manual of chemical and biological methods for seawater analysis. Pergamon Press. Elmsford, New York.</p> <p>Simon, M., and F. Azam. 1989. Protein content and protein synthesis rates of planktonic marine bacteria. Marine Ecology Progress Series. 51, 201-213.</p> <p><em>updated: April 20, 2006</em></p> Dataset ice core Sea ice Southern Ocean Biological and Chemical Oceanography Data Management Office (BCO-DMO) (via DataONE) Southern Ocean Reno ENVELOPE(-58.700,-58.700,-63.817,-63.817) ENVELOPE(-76.781,-65.61,-65.62,-69.25)