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  • 1
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    Global distributions of diazotrophs abundance, biomass and nitrogen fixation rates - Gridded data product (NetCDF) - Contribution to the MAREDAT World Ocean Atlas of Plankton Functional Types (2012)
    PANGAEA
    In:  Supplement to: Luo, Yawei; Doney, Scott C; Anderson, L A; Benavides, Mar; Berman-Frank, I; Bode, Antonio; Bonnet, S; Boström, Kjärstin H; Böttjer, D; Capone, D G; Carpenter, E J; Chen, Yaw-Lin; Church, Matthew J; Dore, John E; Falcón, Luisa I; Fernández, A; Foster, R A; Furuya, Ken; Gomez, Fernando; Gundersen, Kjell; Hynes, Annette M; Karl, David Michael; Kitajima, Satoshi; Langlois, Rebecca; LaRoche, Julie; Letelier, Ricardo M; Marañón, Emilio; McGillicuddy Jr, Dennis J; Moisander, Pia H; Moore, C Mark; Mouriño-Carballido, Beatriz; Mulholland, Margaret R; Needoba, Joseph A; Orcutt, Karen M; Poulton, Alex J; Rahav, Eyal; Raimbault, Patrick; Rees, Andrew; Riemann, Lasse; Shiozaki, Takuhei; Subramaniam, Ajit; Tyrrell, Toby; Turk-Kubo, Kendra A; Varela, Manuel; Villareal, Tracy A; Webb, Eric A; White, Angelicque E; Wu, Jingfeng; Zehr, Jonathan P (2012): Database of diazotrophs in global ocean: abundance, biomass and nitrogen fixation rates. Earth System Science Data, 4, 47-73, https://doi.org/10.5194/essd-4-47-2012
    Details
    Publication Date: 2023-03-27
    Description: The MAREDAT atlas covers 11 types of plankton, ranging in size from bacteria to jellyfish. Together, these plankton groups determine the health and productivity of the global ocean and play a vital role in the global carbon cycle. Working within a uniform and consistent spatial and depth grid (map) of the global ocean, the researchers compiled thousands and tens of thousands of data points to identify regions of plankton abundance and scarcity as well as areas of data abundance and scarcity. At many of the grid points, the MAREDAT team accomplished the difficult conversion from abundance (numbers of organisms) to biomass (carbon mass of organisms). The MAREDAT atlas provides an unprecedented global data set for ecological and biochemical analysis and modeling as well as a clear mandate for compiling additional existing data and for focusing future data gathering efforts on key groups in key areas of the ocean. This is a gridded data product about diazotrophic organisms . There are 6 variables. Each variable is gridded on a dimension of 360 (longitude) * 180 (latitude) * 33 (depth) * 12 (month). The first group of 3 variables are: (1) number of biomass observations, (2) biomass, and (3) special nifH-gene-based biomass. The second group of 3 variables is same as the first group except that it only grids non-zero data. We have constructed a database on diazotrophic organisms in the global pelagic upper ocean by compiling more than 11,000 direct field measurements including 3 sub-databases: (1) nitrogen fixation rates, (2) cyanobacterial diazotroph abundances from cell counts and (3) cyanobacterial diazotroph abundances from qPCR assays targeting nifH genes. Biomass conversion factors are estimated based on cell sizes to convert abundance data to diazotrophic biomass. Data are assigned to 3 groups including Trichodesmium, unicellular diazotrophic cyanobacteria (group A, B and C when applicable) and heterocystous cyanobacteria (Richelia and Calothrix). Total nitrogen fixation rates and diazotrophic biomass are calculated by summing the values from all the groups. Some of nitrogen fixation rates are whole seawater measurements and are used as total nitrogen fixation rates. Both volumetric and depth-integrated values were reported. Depth-integrated values are also calculated for those vertical profiles with values at 3 or more depths.
    Keywords: MAREMIP; MARine Ecosystem Model Intercomparison Project
    Type: Dataset
    Format: application/zip, 1.7 MBytes
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  • 2
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    Abundance and calculated biomass of large-scale distribution from Atlantic nitrogen fixation controlled by iron availability (2013)
    PANGAEA
    Details
    Publication Date: 2023-07-08
    Keywords: AMT17/03; AMT17/04; AMT17/05; AMT17/06; AMT17/08; AMT17/10; Atlantic; Calculated after Luo et al. (2012); DEPTH, water; Diazotrophs, total biomass as carbon; Event label; Iron; Latitude of event; Light microscope; Longitude of event; MAREDAT_Diazotrophs_Collection; Nitrate; Phosphate; Salinity; Temperature, water; Trichodesmium, biomass as carbon; Trichodesmium, carbon per trichome; Trichodesmium abundance, free trichomes; Trichodesmium abundance, total
    Type: Dataset
    Format: text/tab-separated-values, 55 data points
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  • 3
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    Nitrogen fixation rate of large-scale distribution from Atlantic nitrogen fixation controlled by iron availability (2013)
    PANGAEA
    Details
    Publication Date: 2023-07-08
    Keywords: AMT17/01; AMT17/02; AMT17/03; AMT17/04; AMT17/05; AMT17/06; AMT17/07; AMT17/08; AMT17/09; AMT17/10; Atlantic; Calculated after Luo et al. (2012); Date/Time of event; DEPTH, water; Event label; Iron; Latitude of event; Longitude of event; MAREDAT_Diazotrophs_Collection; Nitrate; Nitrogen Fixation (C2H2 Reduction); Nitrogen fixation rate, total; Nitrogen fixation rate, whole seawater; Phosphate; Salinity; Temperature, water
    Type: Dataset
    Format: text/tab-separated-values, 275 data points
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    DATA PANGAEA
  • 4
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    Nitrogen fixation and nitrogen gene abundance of METEOR cruises M77/3 and M77/4 (2014)
    PANGAEA
    In:  Supplement to: Löscher, Carolin R; Großkopf, Tobias; Desai, Falguni; Gill, Diana; Schunck, Harald; Croot, Peter L; Schlosser, Christian; Neulinger, Sven C; Pinnow, Nicole; Lavik, Gaute; Kuypers, Marcel MM; LaRoche, Julie; Schmitz, Ruth A (2014): Facets of diazotrophy in the oxygen minimum zone waters off Peru. The ISME Journal, https://doi.org/10.1038/ismej.2014.71
    Details
    Publication Date: 2023-10-28
    Description: Nitrogen fixation, the biological reduction of dinitrogen gas (N2) to ammonium (NH4+), is quantitatively the most important external source of new nitrogen (N) to the open ocean. Classically, the ecological niche of oceanic N2 fixers (diazotrophs) is ascribed to tropical oligotrophic surface waters, often depleted in fixed N, with a diazotrophic community dominated by cyanobacteria. Although this applies for large areas of the ocean, biogeochemical models and phylogenetic studies suggest that the oceanic diazotrophic niche may be much broader than previously considered, resulting in major implications for the global N-budget. Here, we report on the composition, distribution and abundance of nifH, the functional gene marker for N2 fixation. Our results show the presence of eight clades of diazotrophs in the oxygen minimum zone (OMZ) off Peru. Although proteobacterial clades dominated overall, two clusters affiliated to spirochaeta and archaea were identified. N2 fixation was detected within OMZ waters and was stimulated by the addition of organic carbon sources supporting the view that non-phototrophic diazotrophs were actively fixing dinitrogen. The observed co-occurrence of key functional genes for N2 fixation, nitrification, anammox and denitrification suggests that a close spatial coupling of N-input and N-loss processes exists in the OMZ off Peru. The wide distribution of diazotrophs throughout the water column adds to the emerging view that the habitat of marine diazotrophs can be extended to low oxygen/high nitrate areas. Furthermore, our statistical analysis suggests that NO2- and PO43- are the major factors affecting diazotrophic distribution throughout the OMZ. In view of the predicted increase in ocean deoxygenation resulting from global warming, our findings indicate that the importance of OMZs as niches for N2 fixation may increase in the futur
    Keywords: Climate - Biogeochemistry Interactions in the Tropical Ocean; SFB754
    Type: Dataset
    Format: application/zip, 3 datasets
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  • 5
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    Hydrochemistry measurements and diazotroph abundances (2016)
    PANGAEA
    In:  Supplement to: Martínez-Pérez, Clara; Mohr, Wiebke; Löscher, Carolin R; Dekaezemacker, Julien; Littmann, Sten; Yilmaz, Pelin; Lehnen, Christina; Fuchs, Bernhard M; Lavik, Gaute; Schmitz, Ruth A; LaRoche, Julie; Kuypers, Marcel MM (2016): The small unicellular diazotrophic symbiont, UCYN-A, is a key player in the marine nitrogen cycle. Nature Microbiology, 1, 16163, https://doi.org/10.1038/nmicrobiol.2016.163
    Details
    Publication Date: 2023-10-28
    Description: Microbial dinitrogen (N2) fixation, the nitrogenase enzyme-catalysed reduction of N2 gas into biologically available ammonia, is the main source of new nitrogen (N) in the ocean. For more than 50 years, oceanic N2 fixation has mainly been attributed to the activity of the colonial cyanobacterium Trichodesmium. Other smaller N2-fixing microorganisms (diazotrophs)--in particular the unicellular cyanobacteria group A (UCYN-A)--are, however, abundant enough to potentially contribute significantly to N2 fixation in the surface waters of the oceans. Despite their abundance, the contribution of UCYN-A to oceanic N2 fixation has so far not been directly quantified. Here, we show that in one of the main areas of oceanic N2 fixation, the tropical North Atlantic7, the symbiotic cyanobacterium UCYN-A contributed to N2 fixation similarly to Trichodesmium. Two types of UCYN-A, UCYN-A1 and -A2, were observed to live in symbioses with specific eukaryotic algae. Single-cell analyses showed that both algae-UCYN-A symbioses actively fixed N2, contributing ~20% to N2 fixation in the tropical North Atlantic, revealing their significance in this region. These symbioses had growth rates five to ten times higher than Trichodesmium, implying a rapid transfer of UCYN-A-fixed N into the food web that might significantly raise their actual contribution to N2 fixation. Our analysis of global 16S rRNA gene databases showed that UCYN-A occurs in surface waters from the Arctic to the Antarctic Circle and thus probably contributes to N2 fixation in a much larger oceanic area than previously thought. Based on their high rates of N2 fixation and cosmopolitan distribution, we hypothesize that UCYN-A plays a major, but currently overlooked role in the oceanic N cycle.
    Keywords: Center for Marine Environmental Sciences; Climate - Biogeochemistry Interactions in the Tropical Ocean; MARUM; SFB754
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 6
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    Bacterial nitrogen fixation abundance of METEOR cruise M77/3 (2014)
    PANGAEA
    Details
    Publication Date: 2023-10-28
    Keywords: Bacterial nitrogen fixation, cluster; Bacterial nitrogen fixation, cluster, standard deviation; Bacterial nitrogen fixation, total; Climate - Biogeochemistry Interactions in the Tropical Ocean; CTD/Rosette; CTD-RO; Date/Time of event; DEPTH, water; Event label; Latitude of event; Longitude of event; M77/3; M77/3-CTD109; M77/3-CTD110; M77/3-CTD13; M77/3-CTD14; M77/3-CTD15; M77/3-CTD17; M77/3-CTD19; M77/3-CTD21; M77/3-CTD24; M77/3-CTD25; M77/3-CTD4; M77/3-CTD55; M77/3-CTD57; M77/3-CTD58; M77/3-CTD59; M77/3-CTD6; M77/3-CTD60; M77/3-CTD62; M77/3-CTD63; M77/3-CTD67; M77/3-CTD7; M77/3-CTD70; M77/3-CTD71; Meteor (1986); Sample code/label; SFB754; Standard deviation; Station label
    Type: Dataset
    Format: text/tab-separated-values, 5138 data points
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  • 7
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    Bacterial nitrogen fixation abundance of METEOR cruise M77/4 (2014)
    PANGAEA
    Details
    Publication Date: 2023-10-28
    Keywords: Bacterial nitrogen fixation, cluster; Bacterial nitrogen fixation, cluster, standard deviation; Bacterial nitrogen fixation, total; Climate - Biogeochemistry Interactions in the Tropical Ocean; CTD/Rosette; CTD-RO; Date/Time of event; DEPTH, water; Event label; Latitude of event; Longitude of event; M77/4; M77/4_143; M77/4_152; M77/4_160; M77/4-CTD14; M77/4-CTD18; M77/4-CTD23; M77/4-CTD24; M77/4-CTD29; M77/4-CTD34; M77/4-CTD38; M77/4-CTD39; M77/4-CTD40; M77/4-CTD58; M77/4-CTD68; M77/4-CTD73; M77/4-CTD75; M77/4-CTD79; M77/4-CTD81; M77/4-CTD82; M77/4-CTD90; Meteor (1986); Sample code/label; SFB754; Standard deviation; Station label
    Type: Dataset
    Format: text/tab-separated-values, 1674 data points
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  • 8
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    Nitrogen cycle gene abundance of METEOR cruise M77/3 (2014)
    PANGAEA
    Details
    Publication Date: 2023-10-28
    Keywords: Archael_amoA, standard deviation; Archael_amoA distribution; Climate - Biogeochemistry Interactions in the Tropical Ocean; CTD/Rosette; CTD-RO; Date/Time of event; DEPTH, water; Event label; Functional gene beta amoA; Functional gene beta amoA, standard deviation; Functional gene hzo; Functional gene hzo, standard deviation; Functional gene nirS; Functional gene nirS, standard deviation; Functional gene nrfA; Functional gene nrfA, standard deviation; Latitude of event; Longitude of event; M77/3; M77/3-CTD109; M77/3-CTD110; M77/3-CTD13; M77/3-CTD14; M77/3-CTD15; M77/3-CTD17; M77/3-CTD19; M77/3-CTD21; M77/3-CTD23; M77/3-CTD24; M77/3-CTD25; M77/3-CTD4; M77/3-CTD55; M77/3-CTD57; M77/3-CTD58; M77/3-CTD59; M77/3-CTD6; M77/3-CTD60; M77/3-CTD62; M77/3-CTD63; M77/3-CTD67; M77/3-CTD7; M77/3-CTD70; M77/3-CTD71; Meteor (1986); Sample code/label; SFB754; Station label
    Type: Dataset
    Format: text/tab-separated-values, 3820 data points
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  • 9
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    Global distributions of diazotrophs abundance and biomass - Depth integrated values computed from a collection of source datasets - Contribution to the MAREDAT World Ocean Atlas of Plankton Functional Types (2013)
    PANGAEA
    In:  Supplement to: Luo, Yawei; Doney, Scott C; Anderson, L A; Benavides, Mar; Berman-Frank, I; Bode, Antonio; Bonnet, S; Boström, Kjärstin H; Böttjer, D; Capone, D G; Carpenter, E J; Chen, Yaw-Lin; Church, Matthew J; Dore, John E; Falcón, Luisa I; Fernández, A; Foster, R A; Furuya, Ken; Gomez, Fernando; Gundersen, Kjell; Hynes, Annette M; Karl, David Michael; Kitajima, Satoshi; Langlois, Rebecca; LaRoche, Julie; Letelier, Ricardo M; Marañón, Emilio; McGillicuddy Jr, Dennis J; Moisander, Pia H; Moore, C Mark; Mouriño-Carballido, Beatriz; Mulholland, Margaret R; Needoba, Joseph A; Orcutt, Karen M; Poulton, Alex J; Rahav, Eyal; Raimbault, Patrick; Rees, Andrew; Riemann, Lasse; Shiozaki, Takuhei; Subramaniam, Ajit; Tyrrell, Toby; Turk-Kubo, Kendra A; Varela, Manuel; Villareal, Tracy A; Webb, Eric A; White, Angelicque E; Wu, Jingfeng; Zehr, Jonathan P (2012): Database of diazotrophs in global ocean: abundance, biomass and nitrogen fixation rates. Earth System Science Data, 4, 47-73, https://doi.org/10.5194/essd-4-47-2012
    Details
    Publication Date: 2023-12-09
    Description: The MAREDAT atlas covers 11 types of plankton, ranging in size from bacteria to jellyfish. Together, these plankton groups determine the health and productivity of the global ocean and play a vital role in the global carbon cycle. Working within a uniform and consistent spatial and depth grid (map) of the global ocean, the researchers compiled thousands and tens of thousands of data points to identify regions of plankton abundance and scarcity as well as areas of data abundance and scarcity. At many of the grid points, the MAREDAT team accomplished the difficult conversion from abundance (numbers of organisms) to biomass (carbon mass of organisms). The MAREDAT atlas provides an unprecedented global data set for ecological and biochemical analysis and modeling as well as a clear mandate for compiling additional existing data and for focusing future data gathering efforts on key groups in key areas of the ocean. The present data set presents depth integrated values of diazotrophs abundance and biomass, computed from a collection of source data sets.
    Keywords: 33KB20020923; 33RR20030714; A2/19921126; A2/1992-11-27; AMT8/1999-05-05; AMT8/1999-05-06; AMT8/1999-05-07; AMT8/1999-05-08; AMT8/1999-05-10; AMT8/1999-05-12; AMT8/1999-05-13; AMT8/1999-05-18; AMT8/1999-05-20; AMT8/1999-05-21; AMT8/1999-05-23; AMT8/1999-05-25; AMT8/1999-05-26; AMT8/1999-05-28; AMT8/1999-05-29; AT19641122; AT19641123; AT19641202; AT19641203; AT19641208; Atlantic; Barbados; Barbados_1974-07-09_1; Barbados_1974-07-16_1; Barbados_1974-07-23_1; Barbados_1974-07-28_1; Barbados_1974-08-07_1; Barbados_1974-08-11_1; Barbados_1974-08-21_1; Barbados_1974-08-27_1; Barbados_1974-09-03_1; Barbados_1974-09-10_1; Barbados_1974-09-17_1; Barbados_1974-09-24_1; Barbados_1974-10-03_1; Barbados_1974-10-08_1; Barbados_1974-10-15_1; Barbados_1974-10-22_1; Barbados_1974-10-29_1; Barbados_1974-11-05_1; Barbados_1974-11-12_1; Barbados_1974-11-19_1; Barbados_1974-11-29_1; Barbados_1974-12-03_1; Barbados_1974-12-10_1; Barbados_1974-12-17_1; Barbados_1974-12-23_1; Barbados_1974-12-30_1; Barbados_1975-01-07_1; Barbados_1975-01-14_1; Barbados_1975-01-21_1; Barbados_1975-01-31_1; Barbados_1975-02-04_1; Barbados_1975-02-11_1; Barbados_1975-02-15_1; Barbados_1975-03-05_1; Barbados_1975-03-18_1; Barbados_1975-04-01_1; Barbados_1975-04-18_1; Barbados_1975-04-29_1; Barbados_1975-05-13_1; Barbados_1975-05-21_1; Barbados_1975-05-27_1; Barbados_1975-06-10_1; Barbados_1975-06-24_1; Barbados_1975-07-08_1; Barbados_1975-08-05_1; Barbados_1975-08-25_1; Barbados_1975-10-15_1; Barbados_1975-11-17_1; Barbados_1975-12-10_1; Barbados_1976-01-02_1; Barbados_1976-01-19_1; Barbados_1976-02-10_1; Barbados_1976-03-12_1; Barbados_1976-04-15_1; Barbados_1976-05-14_1; BATS1995-05-15; BATS1996-10-10; Bermuda, Atlantic Ocean; Bottle, Niskin; CAIBEX-I; CAIBEX-I_2; CAIBEX-I_3; CAIBEX-I_5; CAIBEX-I_6; CAIBEX-II; CAIBEX-II_01; CAIBEX-II_02; CAIBEX-II_03; CAIBEX-II_04; CAIBEX-II_05; CAIBEX-II_06; CAIBEX-II_07; CAIBEX-II_08; CAIBOX; CAIBOX_01; CAIBOX_02; CAIBOX_03; CAIBOX_04; CAIBOX_05; CAIBOX_06; CAIBOX_07; CAIBOX_08; CAIBOX_09; CAIBOX_10; CAIBOX_11; CAIBOX_12; CAIBOX_13; CAIBOX_14; CAIBOX_15; CAIBOX_16; CAIBOX_17; Calculated; Calothrix, associated species; Calothrix, carbon per cell; Calothrix abundance, cells; China Sea; Chlorophyll total, areal concentration; CTD, Seabird; CTD/Rosette; CTD-R; CTD-RO; Date/Time of event; Depth, bottom/max; Depth, top/min; DEPTH, water; Diazotrophs, total biomass as carbon; East China Sea; ECS1993-11-15_1; ECS1993-11-15_2; ECS1993-11-15_3; ECS1993-11-15_4; ECS1993-11-15_5; ECS1993-11-15_6; ECS1994-03-15_1; ECS1994-03-15_2; ECS1994-03-15_3; ECS1994-03-15_4; ECS1994-03-15_5; ECS1994-05-05_1; ECS1994-05-05_2; ECS1994-07-05_1; ECS1994-07-05_2; ECS1994-07-05_3; ECS1994-07-05_4; ECS1995-03-28_1; ECS1995-03-28_2; ECS1995-04-17_1; ECS1995-04-17_2; ECS1995-04-17_3; ECS1995-04-17_4; ECS1995-04-17_5; ECS1995-10-01_1; ECS1995-10-01_10; ECS1995-10-01_11; ECS1995-10-01_12; ECS1995-10-01_13; ECS1995-10-01_2; ECS1995-10-01_3; ECS1995-10-01_4; ECS1995-10-01_5; ECS1995-10-01_6; ECS1995-10-01_7; ECS1995-10-01_8; ECS1995-10-01_9; ECS1996-01-04; ECS1996-04-26_1; ECS1996-04-26_2; ECS1996-04-26_3; ECS1996-04-26_4; ECS1996-04-26_5; ECS1996-04-26_6; ECS1996-04-26_7; ECS1996-04-26_8; ECS1996-04-26_9; Event label; GOFLO; Go-Flo bottles; Gomez2004-10-26; Gomez2004-10-30; Gomez2004-11-03; Gomez2004-11-07; Gomez2004-11-11; Gomez2004-11-15; Gomez2004-11-19; Gomez2004-11-23; Gomez2004-11-27; Gomez2004-12-01; Gomez2004-12-05; Gomez2004-12-09; HakuhoMaru2002-12-07; HakuhoMaru2002-12-09; HakuhoMaru2002-12-11; HakuhoMaru2002-12-13; HakuhoMaru2002-12-15; HakuhoMaru2002-12-17; HakuhoMaru2002-12-18; Heterocyst, biomass; Indian Ocean; Iron; Latitude of event; Longitude of event; MAREMIP; MARine Ecosystem Model Intercomparison Project; Measured at sea surface; Meville2002-06-24; Meville2002-06-26; Meville2002-06-28; Meville2002-06-30; Meville2002-07-02; Meville2002-07-03; Meville2002-07-04; Meville2002-07-05; Meville2002-07-06; Meville2002-07-07; Meville2002-07-08; Meville2002-07-11; Meville2002-07-12; Mirai2003-01-15; Mirai2003-01-17; Mirai2003-01-18; Mirai2003-01-20; Mirai2003-01-21; Mirai2003-01-23; Mirai2003-01-24; Mirai2003-01-26; Mirai2003-01-28; MP-6; MP-6_01; MP-6_02; MP-6_03; MP-6_04; MP-6_05; MP-6_06; MP-6_07; MP-6_08; MP-6_09; MP-6_10; MP-6_11; MP-6_12; MP-6_13; MP-6_14; MP-6_15; MP-6_16; MP-6_17; MP-6_19; MP-6_20; MP-6_21; MP-6_22; MP-6_23; MP-9; MP-9_01; MP-9_02; MP-9_03; MP-9_04; MP-9_05; MP-9_06; MP-9_08; MP-9_09; MP-9_10; MP-9_11; MP-9_12; MP-9_13; MP-9_14; MP-9_15; MP-9_16; MP-9_17; MP-9_18; MP-9_19; MP-9_20; MP-9_21; MP-9_22; MP-9_23; MP-9_24; MP-9_25; MP-9_27; MULT; Multiple investigations; MW19950822_21; NA1975-05-25; NA19750526; NA19750527; NA19750528; NA1975-05-29; NA19750530; NA19750531; NA1975-06-01; NA1975-06-02; NA1975-06-03; NA1975-06-04; NA1975-06-05; NA1975-06-06; NewHorizon2003-08-22; NewHorizon2003-08-25; NewHorizon2003-08-26; NewHorizon2003-08-27; NewHorizon2003-08-28; NewHorizon2003-08-30; NewHorizon2003-08-31; NewHorizon2003-09-01; NewHorizon2003-09-03; NewHorizon2003-09-04; NewHorizon2003-09-05; NewHorizon2003-09-07; NewHorizon2003-09-08; NewHorizon2003-09-09; NewHorizon2003-09-11; NewHorizon2003-09-12; NewHorizon2003-09-13; NewHorizon2003-09-14; NIS; Nitrate; North Atlantic; Northeast Atlantic; North Pacific; North Pacific Ocean; Northwest Pacific; NPO1969-08-28; NPO1969-09-01; NPO1969-09-05; NPO1969-09-09; NPO1969-09-11; NPO1969-09-14; NPO1969-09-17; NPO1969-09-19; NPO1969-09-23; NPO1969-09-27; NPO1969-10-01; NPO1969-10-05; NPO1969-10-10; NWP2002-10-21_1; NWP2002-10-21_2; NWP2002-10-21_3; NWP2002-10-21_4; NWP2002-10-21_5; NWP2004-02-11; NWP2004-02-22; NWP2004-05-05; NWP2004-06-26; NWP2004-06-30; NWP2004-07-04; NWP2004-08-07; NWP2004-11-06; NWP2005-03-31; NWP2005-04-22; NWP2005-04-23; NWP2005-04-24; NWP2005-04-25_1; NWP2005-04-25_2; NWP2005-04-26; NWP2005-04-27; NWP2005-04-28; NWP2005-04-29; NWP2005-04-30_1; NWP2005-04-30_2; NWP2005-05-01; NWP2005-08-10; NWP2005-08-15; NWP2005-11-10; NWP2005-12-26; NWP2006-07-03; NWP2006-10-21; NWP2006-12-20; NWP2006-12-25; NWP2007-01-15; OR-I/414_1; OR-I/414_2; OR-I/448; OR-II/034; OR-II/111_1; OR-II/111_2; OR-II/149_1; OR-II/149_2; Phosphate; Richelia, associated species; Richelia, carbon per cell; Richelia abundance, cells; Roger A. Revelle; RV Kilo Moana; Salinity; Sample comment; Sample method; Sargasso Sea; SargassoSea_1973-09-17; SargassoSea_1973-09-19; SargassoSea_1973-09-20; SargassoSea_1973-09-21; SargassoSea_1973-09-28; SargassoSea_1973-09-29; SargassoSea_1973-10-01; SargassoSea_1973-10-02; SargassoSea_1973-10-03; SargassoSea_1974-02-06; SargassoSea_1974-02-08; SargassoSea_1974-02-11; SargassoSea_1974-02-12; SargassoSea_1974-02-13; SargassoSea_1974-02-14; SargassoSea_1974-02-16; SargassoSea_1974-02-17; SargassoSea_1974-02-18; SargassoSea_1974-02-19; SargassoSea_1974-02-20; SargassoSea_1974-02-21; SargassoSea_1974-02-22; SargassoSea_1974-02-26; SargassoSea_1974-02-27; SargassoSea_1974-03-01; SargassoSea_1974-03-02; SargassoSea_1974-03-03; SargassoSea_1974-03-04; SargassoSea_1974-03-05; SargassoSea_1974-08-08; SargassoSea_1974-08-09; SargassoSea_1974-08-10_1; SargassoSea_1974-08-10_2; SargassoSea_1974-08-11; SargassoSea_1974-08-12; SargassoSea_1974-08-13; SargassoSea_1974-08-14; SargassoSea_1974-08-15; SargassoSea_1974-08-16; SargassoSea_1974-08-17; SargassoSea_1974-08-18; SargassoSea_1974-08-19; SargassoSea_1974-08-20; SargassoSea_1974-08-21; Sarmiento de Gamboa; SCS2000-07-04; SCS2000-07-08; SCS2000-07-12; SCS2000-10-05; SCS2000-10-06; SCS2000-10-07; SCS2000-10-08; SCS2000-10-09; SCS2000-10-10; SCS2000-10-11; SCS2000-10-12; SCS2001-03-21; SCS2001-03-22; SCS2001-03-23; SCS2001-03-24; SCS2001-03-25; SCS2001-03-26; SCS2001-03-27; SCS2001-03-28; SCS2001-03-29; SCS2001-03-30; SCS2001-06-28; SCS2001-06-30; SCS2001-07-02; SCS2001-07-04; SCS2001-07-06; SCS2001-10-23; SCS2001-10-25; SCS2001-10-27; SCS2001-10-29; SCS2001-10-31; SCS2002-03-04; SCS2002-03-05; SCS2002-03-06; SCS2002-03-07; SCS2002-03-08; SCS2002-03-09; SCS2002-03-10;
    Type: Dataset
    Format: text/tab-separated-values, 8546 data points
    Location Call Number Expected Availability
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    DATA PANGAEA
  • 10
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    Global distributions of diazotrophs nitrogen fixation rates - Depth integrated values computed from a collection of source datasets - Contribution to the MAREDAT World Ocean Atlas of Plankton Functional Types (2013)
    PANGAEA
    In:  Supplement to: Luo, Yawei; Doney, Scott C; Anderson, L A; Benavides, Mar; Berman-Frank, I; Bode, Antonio; Bonnet, S; Boström, Kjärstin H; Böttjer, D; Capone, D G; Carpenter, E J; Chen, Yaw-Lin; Church, Matthew J; Dore, John E; Falcón, Luisa I; Fernández, A; Foster, R A; Furuya, Ken; Gomez, Fernando; Gundersen, Kjell; Hynes, Annette M; Karl, David Michael; Kitajima, Satoshi; Langlois, Rebecca; LaRoche, Julie; Letelier, Ricardo M; Marañón, Emilio; McGillicuddy Jr, Dennis J; Moisander, Pia H; Moore, C Mark; Mouriño-Carballido, Beatriz; Mulholland, Margaret R; Needoba, Joseph A; Orcutt, Karen M; Poulton, Alex J; Rahav, Eyal; Raimbault, Patrick; Rees, Andrew; Riemann, Lasse; Shiozaki, Takuhei; Subramaniam, Ajit; Tyrrell, Toby; Turk-Kubo, Kendra A; Varela, Manuel; Villareal, Tracy A; Webb, Eric A; White, Angelicque E; Wu, Jingfeng; Zehr, Jonathan P (2012): Database of diazotrophs in global ocean: abundance, biomass and nitrogen fixation rates. Earth System Science Data, 4, 47-73, https://doi.org/10.5194/essd-4-47-2012
    Details
    Publication Date: 2023-12-18
    Description: The MAREDAT atlas covers 11 types of plankton, ranging in size from bacteria to jellyfish. Together, these plankton groups determine the health and productivity of the global ocean and play a vital role in the global carbon cycle. Working within a uniform and consistent spatial and depth grid (map) of the global ocean, the researchers compiled thousands and tens of thousands of data points to identify regions of plankton abundance and scarcity as well as areas of data abundance and scarcity. At many of the grid points, the MAREDAT team accomplished the difficult conversion from abundance (numbers of organisms) to biomass (carbon mass of organisms). The MAREDAT atlas provides an unprecedented global data set for ecological and biochemical analysis and modeling as well as a clear mandate for compiling additional existing data and for focusing future data gathering efforts on key groups in key areas of the ocean. The present data set presents depth integrated values of diazotrophs nitrogen fixation rates, computed from a collection of source data sets.
    Keywords: 33KB20020923; 33RR20030714; Alis; ALOHA2000-07-26; ALOHA2000-11-30; ALOHA2001-03-21; ALOHA2001-06-14; ALOHA2004-11-28; ALOHA2005-02-02; ALOHA2005-03-05; ALOHA2005-06-15; ALOHA2005-07-16; ALOHA2005-08-14; ALOHA2005-09-09; ALOHA2005-10-08; ALOHA2005-11-16; ALOHA2005-12-13; ALOHA2006-01-25; ALOHA2006-02-15; ALOHA2006-03-10; ALOHA2006-04-01; ALOHA2006-05-26; ALOHA2006-06-13; ALOHA2006-07-12; ALOHA2006-08-08; ALOHA2006-09-15; ALOHA2006-10-19; ALOHA2006-11-08; ALOHA2006-12-09; ALOHA2007-02-06; ALOHA2007-03-20; ALOHA2007-05-03; ALOHA2007-06-09; ALOHA2007-07-07; ALOHA2007-08-02; ALOHA2007-09-02; ALOHA2007-12-20; ALOHA2008-01-28; ALOHA2008-02-23; ALOHA2008-05-27; ALOHA2008-06-25; ALOHA2008-07-26; ALOHA2008-08-17; ALOHA2008-10-11; ALOHA2008-12-01; ALOHA2009-01-21; ALOHA2009-02-18; ALOHA2009-04-29; ALOHA2009-05-28; ALOHA2009-07-04; ALOHA2009-07-25; ALOHA2009-09-26; ALOHA2009-11-05; ALOHA2010-04-08; ALOHA2010-05-20; ALOHA2010-06-10; ALOHA2010-07-10; ALOHA2010-08-09; ALOHA2010-09-05; ALOHA2010-10-05; AMT17/01; AMT17/02; AMT17/03; AMT17/04; AMT17/05; AMT17/06; AMT17/07; AMT17/08; AMT17/09; AMT17/10; Arabian Sea; AT19641122; AT19641123; AT19641202; AT19641203; Atalante20080627; Atalante20080628; Atalante20080704; Atalante20080705; Atalante20080709/1; Atalante20080710; Atalante20080712; Atalante20080713; Atalante20080714; Atlantic; BIOSOPE_EGY; BIOSOPE_GYR; BIOSOPE_HLNC; BIOSOPE_MAR; BIOSOPE_UPW; BIOSOPE04-10-28; BIOSOPE04-10-30; BIOSOPE04-11-03; BIOSOPE04-11-04; BIOSOPE04-11-06; BIOSOPE04-11-07; BIOSOPE04-11-08; BIOSOPE04-11-10; BIOSOPE04-11-12; BIOSOPE04-11-20; BIOSOPE04-11-21; BIOSOPE04-11-23; BIOSOPE04-11-24; BIOSOPE04-11-28; BIOSOPE04-12-01; BIOSOPE04-12-02; BIOSOPE04-12-03; BIOSOPE04-12-04; BIOSOPE04-12-05; Bottle, Niskin; CAIBEX-I; CAIBEX-I_1; CAIBEX-I_2; CAIBEX-I_3; CAIBEX-I_4; CAIBEX-I_5; CAIBEX-I_6; CAIBEX-I_7; CAIBEX-II; CAIBEX-II_01; CAIBEX-II_02; CAIBEX-II_03; CAIBEX-II_04; CAIBEX-II_05; CAIBEX-II_06; CAIBEX-II_07; CAIBEX-II_08; CAIBOX; CAIBOX_01; CAIBOX_02; CAIBOX_03; CAIBOX_04; CAIBOX_05; CAIBOX_06; CAIBOX_07; CAIBOX_08; CAIBOX_09; CAIBOX_10; CAIBOX_11; CAIBOX_12; CAIBOX_13; CAIBOX_14; CAIBOX_15; CAIBOX_16; CAIBOX_17; Calculated; Cape Verde; CATO-I/9; Chlorophyll total, areal concentration; CLIMAX_VII/1973-08-18; CLIMAX_VII/1973-08-27; CLIMAX_VII/1973-08-29; CLIMAX_VII/1973-08-31; CLIMAX_VII/1973-09-02; CLIMAX_VII/1973-09-04; CLIMAX_VII/1973-09-07; CLIMAX_VII/1973-09-09; Cook25_7; CTD/Rosette; CTD-RO; D325_Stn-A-01; D325_Stn-C-01; D325_Stn-D-07; D325_Stn-E-01; D325_Stn-F-07; Date/Time of event; Depth, bottom/max; Depth, top/min; DEPTH, water; Diapalis-3; Diapalis-3_1; Diapalis-3_2; Diapalis-3_3; Diapalis-3_4; Diapalis-4; Diapalis-4_1; Diapalis-4_2; Diapalis-4_3; Diapalis-4_4; Diapalis-5; Diapalis-5_1; Diapalis-5_3; Diapalis-5_4; Diapalis-5_5; Diapalis-6; Diapalis-6_1; Diapalis-6_2; Diapalis-6_3; Diapalis-6_4; Diapalis-6_5; Diapalis-6_6; Diapalis-7; Diapalis-7_1; Diapalis-7_2; Diapalis-7_3; Diapalis-7_4; Diapalis-7_6; Diapalis-7_7; Diapalis-9; Diapalis-9_1; Diapalis-9_2; Diapalis-9_3; Diapalis-9_4; Diapalis-9_5; DIAPAZON_Diapalis-3; DIAPAZON_Diapalis-4; DIAPAZON_Diapalis-5; DIAPAZON_Diapalis-6; DIAPAZON_Diapalis-7; DIAPAZON_Diapalis-9; DYFAMED2003-03-26; DYFAMED2003-03-30; DYFAMED2004-01-25; DYFAMED2004-02-24; DYFAMED2004-04-25; DYFAMED2004-05-27; DYFAMED2004-07-01; DYFAMED2004-07-31; DYFAMED2004-08-31; DYFAMED2004-09-18; DYFAMED2004-10-14; Equatorial Pacific; Event label; GoA_StnA2010-03-18; GOFLO; Go-Flo bottles; Gulf of Aqaba; Gundersen_1; Gundersen_2; Hawaiian Islands, North Central Pacific; Hesperides_03a; Hesperides_05a; Hesperides_06a; Hesperides_07a; Hesperides_08a; Hesperides_12a; Hesperides_13a; Hesperides_14a; Hesperides_17a; Hesperides_18a; Hesperides_19a; Hesperides_20a; Hesperides_21a; Hesperides_23a; Hesperides_24a; Hesperides_25a; Hesperides_26a; Hesperides_27a; Hesperides_28a; Hesperides_29a; Hesperides_30a; Hesperides_31a; Hesperides_32a; Hesperides_33a; Hesperides_34a; Hesperides_36a; Hesperides_37a; Hesperides_38a; Hesperides_39a; Hesperides_40a; Hesperides_41a; Hesperides_42a; Heterocyst, nitrogen fixation rate; Iron; KiloMoana20060609/1; KiloMoana20060609/2; KiloMoana20060821; KiloMoana20060826; KiloMoana20060922; KiloMoana20060923; KiloMoana20060925; KiloMoana20060927; KiloMoana20060930; KiloMoana20061009; Latitude of event; LB2008-09-12; LB2008-09-16; Levantine Basin; Ligurian Sea, Mediterranean; Longitude of event; MAREMIP; MARine Ecosystem Model Intercomparison Project; Measured at sea surface; Mediterranean Sea; Mooring (long time); MOORY; MP-6; MP-6_01; MP-6_02; MP-6_03; MP-6_04; MP-6_05; MP-6_06; MP-6_07; MP-6_08; MP-6_09; MP-6_10; MP-6_11; MP-6_12; MP-6_13; MP-6_14; MP-6_15; MP-6_16; MP-6_18; MP-6_19; MP-6_20; MP-6_21; MP-6_22; MP-6_23; MP-9; MP-9_01; MP-9_02; MP-9_03; MP-9_04; MP-9_05; MP-9_06; MP-9_07; MP-9_09; MP-9_10; MP-9_11; MP-9_12; MP-9_13; MP-9_14; MP-9_15; MP-9_16; MP-9_17; MP-9_18; MP-9_19; MP-9_20; MP-9_21; MP-9_22; MP-9_23; MP-9_24; MP-9_25; MP-9_26; MP-9_27; MR07-01/02; MR07-01/03; MR07-01/04; MR07-01/05; MR07-01/06; MR07-01/07; MR07-01/08; MR07-01/09; MR07-01/10; MR07-01/11; Mulholland_2006-07-01; Mulholland_2006-07-02; Mulholland_2006-07-03; Mulholland_2006-07-04; Mulholland_2006-07-05; Mulholland_2006-07-06; Mulholland_2006-07-07; Mulholland_2006-07-08; Mulholland_2006-07-09; Mulholland_2006-07-10; Mulholland_2006-07-11; Mulholland_2006-07-12; Mulholland_2006-07-13; Mulholland_2006-07-14; Mulholland_2006-10-25; Mulholland_2006-10-26; Mulholland_2006-10-27; Mulholland_2006-10-28; Mulholland_2006-10-29; Mulholland_2006-10-30; Mulholland_2006-10-31; Mulholland_2006-11-01; Mulholland_2006-11-02; Mulholland_2006-11-03; Mulholland_2006-11-04; Mulholland_2006-11-05; Mulholland_2006-11-06; Mulholland_2006-11-07; Mulholland_2006-11-08; Mulholland_2006-11-09; Mulholland_2008-05-03_1; Mulholland_2008-05-04_1; Mulholland_2008-05-05_1; Mulholland_2008-05-05_2; Mulholland_2008-05-06_1; Mulholland_2008-05-07_1; Mulholland_2008-05-10_1; Mulholland_2008-05-11_1; Mulholland_2008-05-12_1; Mulholland_2008-05-13_1; Mulholland_2008-05-14_1; Mulholland_2008-05-15_1; Mulholland_2008-05-16_1; Mulholland_2008-05-17_1; Mulholland_2008-05-18_1; Mulholland_2008-05-19_1; Mulholland_2008-05-20_1; Mulholland_2008-05-21_1; Mulholland_2008-05-22_1; Mulholland_2008-05-24_1; Mulholland_2009-08-17_1; Mulholland_2009-08-18_1; Mulholland_2009-08-18_2; Mulholland_2009-08-19_1; Mulholland_2009-08-19_2; Mulholland_2009-08-20_1; Mulholland_2009-08-20_3; Mulholland_2009-08-21_1; Mulholland_2009-08-21_3; Mulholland_2009-08-22_1; Mulholland_2009-08-22_3; Mulholland_2009-08-23; Mulholland_2009-08-24_1; Mulholland_2009-08-24_3; Mulholland_2009-08-25_3; Mulholland_2009-08-26_3; Mulholland_2009-08-27_2; Mulholland_2009-08-27_3; Mulholland_2009-11-04_2; Mulholland_2009-11-05_1; Mulholland_2009-11-08_1; Mulholland_2009-11-09_3; Mulholland_2009-11-10_3; Mulholland_2009-11-11_1; Mulholland_2009-11-18_1; Mulholland_2009-11-18_3; NA19750526; NA19750527; NA19750528; NA19750530; NA19750531; NIS; Nitrate; Nitrogen fixation rate, integrated per day; Nitrogen fixation rate, whole seawater; North Atlantic; Northeast Atlantic; North Pacific; Pacific; Phosphate; PUMP; Rahav_2009-07-13_1; Rahav_2009-07-14_1; Rahav_2009-07-16_1; Rahav_2009-12-07_1; Rees2004-03-05/01; Rees2004-04-05; Rees2004-05-16; Rees2004-05-19/01; Rees2004-05-21/01; Rees2004-07-05/01; Rees2004-09-05/01; Roger A. Revelle; RV Kilo Moana; Salinity; Sample comment; Sample method; Sargasso Sea; SargassoSea_1973-09-17; SargassoSea_1973-09-19; SargassoSea_1973-09-20; SargassoSea_1973-09-21; SargassoSea_1973-09-28; SargassoSea_1973-09-29; SargassoSea_1973-10-01; SargassoSea_1973-10-02; SargassoSea_1973-10-03; SargassoSea_1974-02-06; SargassoSea_1974-02-08; SargassoSea_1974-02-11; SargassoSea_1974-02-13; SargassoSea_1974-02-14; SargassoSea_1974-02-16; SargassoSea_1974-02-17; SargassoSea_1974-02-18; SargassoSea_1974-02-19; SargassoSea_1974-02-20; SargassoSea_1974-02-21; SargassoSea_1974-02-26;
    Type: Dataset
    Format: text/tab-separated-values, 5926 data points
    Location Call Number Expected Availability
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    DATA PANGAEA
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