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Giebel, Helge-Ansgar; Alldag, Pelle; Arndt, Kim Lena; Arnosti, Carol; Badewien, Thomas H; Bakenhus, Insa; Balmonte, John Paul; Billerbeck, Sara; Henkel, Rohan; Kuerzel, Birgit; Meier, Daniela; Meyerjürgens, Jens; Milke, Felix; Voß, Daniela; Winkler, Holger; Wolterink, Mathias; Zielinski, Oliver; Simon, Meinhard (2020): Hydrography, biogeochemistry, microbial population, growth and substrate dynamics between subarctic and subantarctic waters in the Pacific Ocean during the cruises SO248 and SO254 with RV Sonne [dataset]. PANGAEA, https://doi.org/10.1594/PANGAEA.918500

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Abstract:
Data presented here were collected during the two cruises SO248 and SO254 with RV SONNE in the Pacific Ocean at 25 stations along a transect closely following 180° longitude E/W between 52.1°S southeast of New Zealand and 58.9°N in the Bering Sea. The first cruise SO248 was conducted from Auckland, New Zealand, to Dutch Harbor, USA (May 1st, 2016 - June 3rd, 2016) and the second (SO254) took place from January 26th, 2017 - February 27th, 2017 and started and ended in Auckland, New Zealand. The data comprises hydrographical, chemical, biogeochemical and biological parameters.
Keyword(s):
Bacteria; biogeochemistry; biogeography; CARD-FISH; cyanobacteria; flow cytometry; heterotrophic prokaryotic production; HNA; LNA; Pacific Ocean; RV Sonne; SO248; SO254
Supplement to:
Giebel, Helge-Ansgar; Arnosti, Carol; Badewien, Thomas H; Bakenhus, Insa; Balmonte, John Paul; Billerbeck, Sara; Dlugosch, Leon; Henkel, Rohan; Kuerzel, Birgit; Meyerjürgens, Jens; Milke, Felix; Voß, Daniela; Wienhausen, Gerrit; Wietz, Matthias; Winkler, Holger; Wolterink, Mathias; Simon, Meinhard (2021): Microbial Growth and Organic Matter Cycling in the Pacific Ocean Along a Latitudinal Transect Between Subarctic and Subantarctic Waters. Frontiers in Marine Science, 8, https://doi.org/10.3389/fmars.2021.764383
Related to:
Balmonte, John Paul; Simon, Meinhard; Giebel, Helge-Ansgar; Arnosti, Carol (2021): A sea change in microbial enzymes: Heterogeneous latitudinal and depth‐related gradients in bulk water and particle‐associated enzymatic activities from 30°S to 59°N in the Pacific Ocean. Limnology and Oceanography, 66(9), 3489-3507, https://doi.org/10.1002/lno.11894
Simon, Meinhard (2016): RV SONNE SO248 (BacGeoPac) Cruise Report / Fahrtbericht, Auckland, New Zealand: May 1st, 2016 Dutch Harbor, USA: June 3rd, 2016. Institute for Chemistry and Biology of the Marine Environment (ICBM), University of Oldenburg, 103 pp, https://doi.org/10.2312/cr_so248
Simon, Meinhard (2017): RV SONNE SO254 Cruise Report / Fahrtbericht, Auckland, New Zealand: January 26th, 2017 - Auckland, New Zealand: February 27th, 2017. Institute for Chemistry and Biology of the Marine Environment, University of Oldenburg, 99 pp, https://doi.org/10.2312/cr_so254
Project(s):
Ökologie, Physiologie und Molekularbiologie der Roseobacter-Gruppe: Aufbruch zu einem systembiologischen Verständnis einer global wichtigen Gruppe mariner Bakterien (TRR51)
Funding:
Federal Ministry of Education and Research (BMBF), grant/award no. 03G0248A: SO248 BacGeoPac
Federal Ministry of Education and Research (BMBF), grant/award no. 03G0254A: SO254 PoriBacNewZ
German Research Foundation (DFG), grant/award no. 34509606: Ökologie, Physiologie und Molekularbiologie der Roseobacter-Gruppe: Aufbruch zu einem systembiologischen Verständnis einer global wichtigen Gruppe mariner Bakterien
Coverage:
Median Latitude: 4.414063 * Median Longitude: 179.395281 * South-bound Latitude: -52.123500 * West-bound Longitude: 176.999300 * North-bound Latitude: 58.900000 * East-bound Longitude: -176.475300
Date/Time Start: 2016-05-02T16:51:00 * Date/Time End: 2017-02-15T20:32:00
Minimum Elevation: -6229.6 m * Maximum Elevation: -566.0 m
Event(s):
SO248_1-1 * Latitude: -30.000820 * Longitude: 176.999300 * Date/Time: 2016-05-02T16:51:55 * Elevation: -4268.2 m * Location: South Pacific Ocean * Campaign: SO248 (BacGeoPac) * Basis: Sonne_2 * Method/Device: CTD/Rosette (CTD-RO)
SO248_2-1 * Latitude: -26.992830 * Longitude: 178.213280 * Date/Time: 2016-05-03T17:40:33 * Elevation: -4196.7 m * Location: South Pacific Ocean * Campaign: SO248 (BacGeoPac) * Basis: Sonne_2 * Method/Device: CTD/Rosette (CTD-RO)
SO248_3-1 * Latitude: -14.999970 * Longitude: -178.000000 * Date/Time: 2016-05-06T20:49:11 * Elevation: -1526.6 m * Location: South Pacific Ocean * Campaign: SO248 (BacGeoPac) * Basis: Sonne_2 * Method/Device: CTD/Rosette (CTD-RO)
Parameter(s):
#NameShort NameUnitPrincipal InvestigatorMethod/DeviceComment
1Event labelEventBadewien, Thomas H
2Station labelStationGiebel, Helge-AnsgarCTD station
3Station labelStationGiebel, Helge-Ansgarin publication
4DATE/TIMEDate/TimeBadewien, Thomas HGeocode
5LATITUDELatitudeBadewien, Thomas HGeocode
6LONGITUDELongitudeBadewien, Thomas HGeocode
7ELEVATIONElevationm a.s.l.Badewien, Thomas HGeocode
8DEPTH, waterDepth watermBadewien, Thomas HGeocode
9Biogeographical provinceBG provinceGiebel, Helge-AnsgarBiogeographical province after Longhurst (2006)
10Pressure, waterPressdbarBadewien, Thomas HCTD, Sea-Bird, SBE 911plus [SN: 09-1266]
11Temperature, waterTemp°CZielinski, OliverCTD, SEA-BIRD SBE 911plus, SN 5828 / SN 4529ITS-90, mean of Sensor 1+2 for cruise SO254
12Temperature, water, potentialTpot°CBadewien, Thomas HCalculated
13ConductivityCondmS/cmZielinski, OliverCTD, SEA-BIRD SBE 911plus, SN 5828 / SN 4529Mean of Sensor 1+2
14SalinitySalBadewien, Thomas HCTD, Sea-Bird, SBE 911plus [SN: 09-1266]PSS78
15SalinitySalBadewien, Thomas HCalculatedTEOS10
16Density, sigma-theta (0)Sigma-thetakg/m3Zielinski, OliverCalculatedMean of Sensor 1+2 only for Cruise SO254
17Sound velocity in waterSVm/sZielinski, Oliver
18OxygenO2µmol/kgBadewien, Thomas HOxygen optode, Aanderaa, type 4831F
19Turbidity (Nephelometric turbidity unit)TurbidityNTUBadewien, Thomas HFluorometer, WET Labs ECO AFL/FL
20Fluorescence, chlorophyllF chlµg/lBadewien, Thomas HFluorometer, WET Labs ECO AFL/FL
21Chlorophyll aChl aµg/lGiebel, Helge-AnsgarAcetone extraction, fluorescence determination
22Nitrogen, organic, particulatePONµg/lGiebel, Helge-AnsgarCombustion by FlashEA 1112 CHN-analyzer
23Carbon, organic, particulatePOCµg/lGiebel, Helge-AnsgarCombustion by FlashEA 1112 CHN-analyzer
24Carbon, organic, particulate/Nitrogen, organic, particulate ratioPOC/PONGiebel, Helge-AnsgarCalculatedCalculated: POC/12:PON/14, mol%
25SilicateSi(OH)4µmol/lGiebel, Helge-AnsgarFluorescence determinationDL <0.1 µmol/l
26Phosphate[PO4]3-µmol/lGiebel, Helge-AnsgarFluorescence determinationDL <0.04 µmol/l
27Nitrogen oxideNOxµmol/lGiebel, Helge-AnsgarFluorescence determinationDL <0.32 µmol/l
28Nitrite[NO2]-µmol/lGiebel, Helge-AnsgarFluorescence determinationDL <0.07 µmol/l
29Nitrate[NO3]-µmol/lGiebel, Helge-AnsgarCalculatedNO3 = NOx - NO2
30Amino acid, total dissolved freeDFAAnmol/lGiebel, Helge-AnsgarHigh performance liquid chromatography (HPLC) using an Agilent 1200 HPLC device after an ortho-phthaldialdehyde precolumn derivatization (Lindroth and Mopper, 1979) with slight modifications as described by Lunau et al. (2006)
31Amino acid, total dissolved free uptakeDFAA uptnmol/l/hSimon, MeinhardIncorporation of 3H-Amino acid mix (Simon et al. 2004, doi:10.4319/lo.2004.49.4.1035; 2007, doi:10.4319/lo.2007.52.1.0085)
32Amino acid, total hydrolysable dissolvedTHDAAnmol/lGiebel, Helge-AnsgarHPLC after Lindroth and Mopper (1979) with slight modifications as described by Lunau et al. (2006)
33Amino acids, dissolved combinedDCAAnmol/lGiebel, Helge-AnsgarCalculated; DCAA = THDAA - DFAA; after Lunau et al. (2006)
34Carbohydrates, dissolved, neutral freeDFCHOnmol/lGiebel, Helge-AnsgarHigh Performance Liquid Chromatography (HPLC) using anion-exchange columns by pulsed amperometric detection according to Mopper et al. (1992)
35Carbohydrates, dissolved, neutral free, uptakeDFCHO uptnmol/l/hSimon, MeinhardIncorporation of 3H-Glucose (Simon et al. 2004, doi:10.4319/lo.2004.49.4.1035; 2007, doi:10.4319/lo.2007.52.1.0085)
36Carbohydrates, total hydrolyzableTHCHOnmol/lGiebel, Helge-AnsgarHigh Performance Liquid Chromatography (HPLC) using anion-exchange columns by pulsed amperometric detection according to Mopper et al. (1992)
37Prokaryotes, heterotrophProk het#/mlGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]data corrected by substraction of population(s) of cyanobacteria within the HNA gate, Prokaryotes = HNA-cyanos2+LNA
38High nucleic acid bacteriaHNA#/mlGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]high nucleic acid (HNA) content prokaryotic cells, data corrected by substraction of population of cyanobacteria within the HNA gate, HNA-cyanobacteria population 2
39Bacteria, heterotrophic with relatively low DNA contentLNA#/mlGiebel, Helge-Ansgarlow nucleic acid (LNA) content prokaryotic cells
40High nucleic acid bacteriaHNA%Giebel, Helge-AnsgarCalculated
41Low nucleic acid bacteriaLNA%Giebel, Helge-AnsgarCalculated
42CyanobacteriaCyanobact#/mlGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]Cyanobacteria = sum of Cyanobacteria population 1 + Cyanobacteria population 2
43CyanobacteriaCyanobact#/mlGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]Population 1, main population aside bacterial population
44CyanobacteriaCyanobact#/mlGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]Population 2, Cyanobacterial population within HNA.
45CyanobacteriaCyanobacteria%Giebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]Calculated: Cyanobacteria / heterotrophic Prokaryotes*100
46Flagellates+algaeFlagellates+algae#/mlGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]Size limitation due to device, <50 µm
47Prokaryotes, cell size, forward scatterProk FSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]
48High nucleic acid bacteria, cell size, forward scatterHNA FSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]
49Low nucleic acid bacteria, cell size, forward scatterLNA FSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]
50Cyanobacteria, cell size, forward scatterCyanobacteria FSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]Population 1
51Cyanobacteria, cell size, forward scatterCyanobacteria FSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]Population 2
52Flagellates+algae, cell size, forward scatterFlagellates+algae FSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]
53Prokaryotes, cell size, relativeProk cell size relGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [calibration of the forward scatter (FSC), only relative cell size due to calibration after Giebel et al. (2019)]Given is the relative cell size in "relative µm" due to calibration after Giebel et al. (2019)
54High nucleic acid bacteria, cell size, relativeHNA cell size relGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [calibration of the forward scatter (FSC), only relative cell size due to calibration after Giebel et al. (2019)]Given is the relative cell size in "relative µm" due to calibration after Giebel et al. (2019)
55Low nucleic acid bacteria, cell size, relativeLNA cell size relGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [calibration of the forward scatter (FSC), only relative cell size due to calibration after Giebel et al. (2019)]Given is the relative cell size in "relative µm" due to calibration after Giebel et al. (2019)
56Prokaryotes, heterotroph, cell size, side scatterProk het SSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]
57High nucleic acid bacteria, cell size, side scatterHNA SSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]
58Low nucleic acid bacteria, cell size, side scatterLNA SSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]
59Cyanobacteria, cell size, side scatterCyanobacteria SSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]Population 1
60Cyanobacteria, cell size, side scatterCyanobacteria SSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]Population 2
61Flagellates+algae, cell size, side scatterFlagellates+algae SSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [SybrGreenI staining]
62PicoplanktonPicopl#/mlGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [autofluorescence (AF)]
63NanoplanktonNanopl#/mlGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [autofluorescence (AF)]
64MicroplanktonMicropl#/mlGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [autofluorescence (AF)]
65EukaryotesEuka#/mlGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [autofluorescence (AF)]Eucaryotes = sum (Pico + Nano + Micro)
66Picoplankton, cell size, forward scatterPicopl FSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [autofluorescence (AF)]
67Nanoplankton, cell size, forward scatterNanopl FSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [autofluorescence (AF)]
68Microplankton, cell size, forward scatterMicropl FSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [autofluorescence (AF)]
69Eukaryotes, cell size, forward scatterEukaryotes FSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [autofluorescence (AF)]
70Picoplankton, cell size, relativePicopl cell size relGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [autofluorescence, calibration of the forward scatter (FSC)]Given is the relative cell size in "relative µm" due to calibration after Giebel et al. (2019)
71Nanoplankton, cell size, relativeNanopl cell size relGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [autofluorescence, calibration of the forward scatter (FSC)]Given is the relative cell size in "relative µm" due to calibration after Giebel et al. (2019)
72Microplankton, cell size, relativeMicropl cell size relGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [autofluorescence, calibration of the forward scatter (FSC)]Given is the relative cell size in "relative µm" due to calibration after Giebel et al. (2019)
73Eukaryotes, cell size, relativeEukaryotes cell size relGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [autofluorescence, calibration of the forward scatter (FSC)]Given is the relative cell size in "relative µm" due to calibration after Giebel et al. (2019)
74Picoplankton, cell size, side scatterPicopl SSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [autofluorescence (AF)]related to cell granularity: cell-structure, -inclusions, -size, -shape
75Nanoplankton, cell size, side scatterNanopl SSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [autofluorescence (AF)]related to cell granularity: cell-structure, -inclusions, -size, -shape
76Microplankton, cell size, side scatterMicropl SSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [autofluorescence (AF)]related to cell granularity: cell-structure, -inclusions, -size, -shape
77Eukaryotes, cell size, side scatterEukaryotes SSCGiebel, Helge-AnsgarFlow Cytometer, BD Biosciences, C6 [autofluorescence (AF)]related to cell granularity: cell-structure, -inclusions, -size, -shape
78Prokaryotes, heterotroph, carbon productionProk het C prodng/l/hSimon, MeinhardIncorporation of 14C-leucine (Simon and Azam, 1989, http://www.int-res.com/articles/meps/51/m051p201.pdf; Simon et al. 2004, doi:10.4319/lo.2004.49.4.1035)
79Prokaryotes, heterotroph, nitrogen productionProk het N prodng/l/hSimon, MeinhardIncorporation of 14C-leucine (Simon and Azam, 1989, http://www.int-res.com/articles/meps/51/m051p201.pdf; Simon et al. 2004, doi:10.4319/lo.2004.49.4.1035)
80Prokaryotes, heterotroph, protein productionProk het protein prodng/l/hSimon, MeinhardIncorporation of 14C-leucine (Simon and Azam, 1989, http://www.int-res.com/articles/meps/51/m051p201.pdf; Simon et al. 2004, doi:10.4319/lo.2004.49.4.1035)
81Prokaryotes, growth rateProk µ1/daySimon, MeinhardIncorporation of 14C-leucine (Simon and Azam, 1989, http://www.int-res.com/articles/meps/51/m051p201.pdf; Simon et al. 2004, doi:10.4319/lo.2004.49.4.1035)
82Generation timeGen timedaySimon, MeinhardIncorporation of 14C-leucine (Simon and Azam, 1989, http://www.int-res.com/articles/meps/51/m051p201.pdf; Simon et al. 2004, doi:10.4319/lo.2004.49.4.1035)prokaryotic
83Prokaryotes, heterotroph, biomass production in mass proteinProk het biom prod proteinµg/l/daySimon, MeinhardIncorporation of 14C-leucine (Simon and Azam, 1989, http://www.int-res.com/articles/meps/51/m051p201.pdf; Simon et al. 2004, doi:10.4319/lo.2004.49.4.1035)HPBP
84Turnover rate, amino acids, dissolved, freek amino acids dissolved free1/daySimon, MeinhardIncorporation of 3H-Amino acid mix (Simon et al. 2004, doi:10.4319/lo.2004.49.4.1035; 2007, doi:10.4319/lo.2007.52.1.0085)
85Turnover rate, glucosek glc1/daySimon, MeinhardIncorporation of 3H-Glucose (Simon et al. 2004, doi:10.4319/lo.2004.49.4.1035; 2007, doi:10.4319/lo.2007.52.1.0085)
86Turnover rate, acetatek acetate1/daySimon, MeinhardIncorporation of 3H-acetate (Simon et al. 2007, doi:10.4319/lo.2007.52.1.0085)
87Hydrolysis rate, beta-GlucoseHydrol rate b-Glcnmol/l/hBalmonte, John PaulBreakdown of fluorescent substrate analoga (Obayashi and Suzuki, 2005, Limnol Oceanogr; Balmonte et al ., 2018, Environ Microbiol)beta-glucopyranoside, beta-glucosidase activity, More enzyme activity data can be accessed at the BCO-DMO database (https://www.bco-dmo.org/; doi:10.26008/1912/bco-dmo.743274.1)
88Hydrolysis rate, LeucineHydrol rate Leucinenmol/l/hBalmonte, John PaulBreakdown of fluorescent substrate analoga (Obayashi and Suzuki, 2005, Limnol Oceanogr; Balmonte et al ., 2018, Environ Microbiol)petidase activity, More enzyme activity data can be accessed at the BCO-DMO database (https://www.bco-dmo.org/; doi:10.26008/1912/bco-dmo.743274.1)
89SynechococcusSynechococcus#/mlGiebel, Helge-AnsgarBD FACS ARIA3 Flow Cytometer, autofluorescence (AF)surface populations were extrapolated, if partly under threshold.
90Synechococcus, cell size, forward scatterSynechococcus FSCGiebel, Helge-AnsgarBD FACS ARIA3 Flow Cytometer, autofluorescence (AF)
91Synechococcus, cell size, side scatterSynechococcus SSCGiebel, Helge-AnsgarBD FACS ARIA3 Flow Cytometer, autofluorescence (AF)related to cell granularity and complexity: cell-structure, -inclusions, -size, -shape
92ProchlorococcusProchlorococcus#/mlGiebel, Helge-AnsgarBD FACS ARIA3 Flow Cytometer, autofluorescence (AF)surface populations were extrapolated, if partly under threshold.
93Prochlorococcus, cell size, forward scatterProchlorococcus FSCGiebel, Helge-AnsgarBD FACS ARIA3 Flow Cytometer, autofluorescence (AF)
94Prochlorococcus, cell size, side scatterProchlorococcus SSCGiebel, Helge-AnsgarBD FACS ARIA3 Flow Cytometer, autofluorescence (AF)related to cell granularity and complexity: cell-structure, -inclusions, -size, -shape
95Mixed layer depthMLDmGiebel, Helge-Ansgar
96Forel-Ule indexFUI#Zielinski, Oliver#2 = 2-3, #1 = 1-2
97Depth of Secchi Diskz(SD)mZielinski, Oliver
98Depth, relativeDepth relmZielinski, OliverCalculated from downwelling photosynthetically active radiation PAR Ed, integrated from 400 - 700 nmof 1% photosynthetically active radiation, doi:10.1594/PANGAEA.911985
99Depth, relativeDepth relmZielinski, OliverCalculated from downwelling photosynthetically active radiation PAR Ed, integrated from 400 - 700 nmof 10% photosynthetically active radiation, doi:10.1594/PANGAEA.911985
100Cytophaga-FlavobacteriaCytophaga-Flavobacteria%Bakenhus, InsaCatalyzed reporter deposition fluorescence in situ hybridisation (CARD-FISH), % of the DAPI positive stained cells
101Cytophaga-Flavobacteria, cellsCytophaga-Flavobacteria cells105 #/mlBakenhus, InsaCatalyzed reporter deposition fluorescence in situ hybridisation (CARD-FISH)
102RoseobacterRoseob%Bakenhus, InsaCatalyzed reporter deposition fluorescence in situ hybridisation (CARD-FISH), % of the DAPI positive stained cells
103Roseobacter, cellsRoseobacter cells105 #/mlBakenhus, InsaCatalyzed reporter deposition fluorescence in situ hybridisation (CARD-FISH)
104SAR11SAR11%Bakenhus, InsaCatalyzed reporter deposition fluorescence in situ hybridisation (CARD-FISH), % of the DAPI positive stained cellsFor applied probe see Bakenhus et al. 2018, Front Microbiol, doi:10.1111/1462-2920.14383
105SAR11, cellsSAR11 cells105 #/mlBakenhus, InsaCatalyzed reporter deposition fluorescence in situ hybridisation (CARD-FISH)
106GammaproteobacteriaGammaproteobacteria%Bakenhus, InsaCatalyzed reporter deposition fluorescence in situ hybridisation (CARD-FISH), % of the DAPI positive stained cells
107Gammaproteobacteria, cellsGammaproteobacteria cells105 #/mlBakenhus, InsaCatalyzed reporter deposition fluorescence in situ hybridisation (CARD-FISH)
108PolaribacterPolaribacter%Bakenhus, InsaCatalyzed reporter deposition fluorescence in situ hybridisation (CARD-FISH), % of the DAPI positive stained cells
109Polaribacter, cellsPolaribacter cells105 #/mlBakenhus, InsaCatalyzed reporter deposition fluorescence in situ hybridisation (CARD-FISH)
110Roseobacter clade affiliated cluster, Planktomarina temperataRCA Planktomarina temperata%Bakenhus, InsaCatalyzed reporter deposition fluorescence in situ hybridisation (CARD-FISH), % of the DAPI positive stained cells
111Roseobacter clade affiliated cluster, Planktomarina temperata, cellsRCA Planktomarina temperata cells105 #/mlBakenhus, InsaCatalyzed reporter deposition fluorescence in situ hybridisation (CARD-FISH)
Size:
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