{"@context":{"content":"http://purl.org/rss/1.0/modules/content/","dc":"http://purl.org/dc/terms/","foaf":"http://xmlns.com/foaf/0.1/","og":"http://ogp.me/ns#","rdfs":"http://www.w3.org/2000/01/rdf-schema#","sioc":"http://rdfs.org/sioc/ns#","sioct":"http://rdfs.org/sioc/types#","skos":"http://www.w3.org/2004/02/skos/core#","xsd":"http://www.w3.org/2001/XMLSchema#","owl":"http://www.w3.org/2002/07/owl#","rdf":"http://www.w3.org/1999/02/22-rdf-syntax-ns#","rss":"http://purl.org/rss/1.0/","site":"https://osprey.bco-dmo.org/ns#","odo":"http://ocean-data.org/schema/","emo":"http://ocean-data.org/schema/entity-matching#","bibo":"http://purl.org/ontology/bibo/","crypto":"http://id.loc.gov/vocabulary/preservation/cryptographicHashFunctions/","bcodmo":"http://lod.bco-dmo.org/id/","tw":"http://tw.rpi.edu/schema/","dcat":"http://www.w3.org/ns/dcat#","time":"http://www.w3.org/2006/time#","geo":"http://www.w3.org/2003/01/geo/wgs84_pos#","geosparql":"http://www.opengis.net/ont/geosparql#","sf":"http://www.opengis.net/ont/sf#","void":"http://rdfs.org/ns/void#","sd":"http://www.w3.org/ns/sparql-service-description#","dctype":"http://purl.org/dc/dcmitype/","prov":"http://www.w3.org/ns/prov#","schema":"http://schema.org/","geolink":"http://schema.geolink.org/1.0/base/main#","spdx":"http://spdx.org/rdf/terms#","bcodmo_vocab":"http://schema.bco-dmo.org/"},"@id":"http://lod.bco-dmo.org/id/dataset/2348#graph","@graph":[{"http://lod.bco-dmo.org/id/dataset/2348":{"@id":"http://lod.bco-dmo.org/id/dataset/2348","@type":["http://ocean-data.org/schema/DeploymentDatasetCollection","http://www.w3.org/ns/dcat#Dataset","http://ocean-data.org/schema/Dataset"],"http://ocean-data.org/schema/hasAcquisitionDescription":[{"@value":"<div><p>Sampling methods for recovery of chlorophyll <em>a</em> and bacteria from sea ice cores follows those described in:<br />\nGarrison, 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>\n<p>Recommendations for reporting were used as outlined by:<br />\nHorner, 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>\n<pre>\n#  Ice core bacteria data from Southern Ocean GLOBEC\n#     C. Fritsen and F. Stewart\n#            * BactAbun = bacterial abundance = cells m-3\n#            * BactBio = bacterial biomass = mg C m-3 = ug C l-1\n#            * chla = mg chla m-3 = ug chla l-1\n#            * sect_top_depth = depth(m) at top of core section\n</pre></div>","@type":"rdf:HTML"}],"http://ocean-data.org/schema/hasBriefDescription":[{"@value":"Ice core bacteria data","@language":"en-US"}],"http://purl.org/dc/terms/description":[{"@value":"<div><h2>Bacteria Abundance, Biomass and Chlorophyll <em>a</em> in Ice Cores</h2>\n<p><strong>NOTES:</strong><br />\nNBP0104: Cores labelled with \"DNA\" were collected for DNA analysis.</p>\n<pre>\n\n<strong>Contributor:</strong>\nDr. Christian Fritsen\nUniversity and Community College System of Nevada \nDesert Research Institute\nDiv. of Earth and Ecosystem Sciences\n2215 Raggio Parkway\nReno, NV 89512\n\nOffice: 775/673-7487\n\n</pre><h3>BG 235 - Methods used for chlorophyll <em>a</em> (chla) analysis and bacteria biomass determination</h3>\n<p><strong>Core Sampling techniques:</strong></p>\n<p>Sampling methods for recovery of chlorophyll <em>a</em> and bacteria from sea ice cores follows those described in:<br />\nGarrison, 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>\n<p>Recommendations for reporting were used as outlined by:<br />\nHorner, 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>\n<p><strong>Analytic Techniques:</strong></p>\n<p>Chla (mg m<sup>-3</sup>):</p>\n<ul>\n<li>determined fluorometrically (Turner Designs 10AU Fluorometer) following extraction in 90% acetone (Parsons <em>et al</em>., 1984)</li>\n<li>ice core chla corrected to account for chla in filtered sea water (FSW) added to core sections during melting</li>\n</ul>\n<p>Bacteria cell abundance (cells m<sup>-3</sup>) and biomass (mg C m<sup>-3</sup>):</p>\n<p>LMG 0106</p>\n<ul>\n<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>\n<li>bacteria enumerated using epifluorescence microscopy and sized using digital images taken with Image Pro Plus</li>\n<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>\n<li>ice core samples corrected for FSW dilution</li>\n</ul>\n<p>NBP 0104</p>\n<ul>\n<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>\n<li>bacteria enumerated using epifluorescence microscopy and sized using digital images taken with Image Pro Plus</li>\n<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>\n<li>ice core samples corrected for FSW dilution</li>\n</ul>\n<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>\n<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>\n<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>\n<p><em>updated: April 20, 2006</em></p></div>","@type":"rdf:HTML"}],"http://www.w3.org/2000/01/rdf-schema#label":[{"@value":"bacteria_ice","@type":"xsd:string"}],"http://ocean-data.org/schema/hasProcessingDescription":[{"@value":"<div><p>Sampling methods for recovery of chlorophyll <em>a</em> and bacteria from sea ice cores follows those described in:<br />\nGarrison, 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>\n<p>Recommendations for reporting were used as outlined by:<br />\nHorner, R. <em>et al.</em>,(1992), Ecology of Sea Ice Biota. 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