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  • 1
    Online Resource
    Online Resource
    Tokyo :Springer Japan,
    Keywords: Food science. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (637 pages)
    Edition: 1st ed.
    ISBN: 9784431551300
    DDC: 579
    Language: English
    Note: Intro -- Preface -- Contents -- Part I: Diversity, Biology, and Ecology -- Chapter 1: Protistan Diversity in Environmental Molecular Surveys -- 1.1 Introduction -- 1.2 Protists in Marine Environments -- 1.3 Identification of Marine Planktonic Protists -- 1.4 Environmental Sequencing of Phylogenetic Marker Genes -- 1.5 Fingerprinting Analysis for Community Comparison -- 1.6 Beyond Sequences and Back to the Cells -- 1.7 The Genomic Era -- 1.8 Closing Remarks -- References -- Chapter 2: Unusual Features of Dinokaryon, the Enigmatic Nucleus of Dinoflagellates -- 2.1 Introduction -- 2.2 Phylogeny of Dinoflagellates -- 2.3 The Dinokaryon -- 2.3.1 Genome, Chromosome, and DNA -- 2.3.2 Transcription and Spliced Leader Trans-Splicing -- 2.3.3 Mitosis -- 2.3.4 Nucleofilament -- 2.3.5 Proposed Models for Chromosome Architecture -- 2.3.6 Nuclear Proteins -- 2.3.7 HCc Family -- 2.3.8 Dinaps and Their Associating Proteins -- 2.3.9 Lamin and Lamin-Like Proteins -- 2.3.10 NP23 and DVNP -- 2.3.11 Histones and Histone-Related Proteins -- 2.3.12 Other Nuclear Proteins -- 2.4 Concluding Remarks -- References -- Chapter 3: Diversity of Microbial Eukaryotes in Deep Sea Chemosynthetic Ecosystems Illuminated by Molecular Techniques -- 3.1 Introduction -- 3.2 Microbial Eukaryotes in the Ecosystems of Hydrothermal Vents -- 3.3 Microbial Eukaryotes in the Ecosystems of Cold Seeps -- 3.4 Perspectives -- References -- Chapter 4: Biology, Diversity and Ecology of Free-Living Heterotrophic Flagellates -- 4.1 Introduction -- 4.2 Opisthokonta -- 4.3 Amoebozoa (Amoebobionta) -- 4.4 Excavata -- 4.5 Archaeplastida (Plantae) -- 4.6 Stramenopiles -- 4.7 Alveolata -- 4.8 Rhizaria -- 4.9 Other Flagellates -- References -- Chapter 5: Basal Lineages of Green Algae - Their Diversity and Phylogeny -- 5.1 Introduction -- 5.2 Classification of Primitive Green Algae -- 5.2.1 Streptophyta. , 5.2.1.1 Class Mesostigmatophyceae Marin et Melkonian 1999 -- 5.2.2 Chlorophyta -- 5.2.2.1 Order Prasinococcales (Clade VI) -- 5.2.2.2 Order Palmophyllales Zechman, Verbruggen, Leliaert, Ashworth, MA Buchheim, Fawley, H Spalding, Pueschel, JA Buchheim, Verghese et Hanisak 2010 -- 5.2.2.3 Pyramimonadales sensu Melkonian 1990 (Clade I) -- 5.2.2.4 Mamiellophyceae Marin et Melkonian 2010 (Clade II) -- 5.2.2.4.1 Mamiellales Moestrup 1984 emend. Marin et Melkonian 2010 -- Mamiellaceae Moestrup 1984 emend. Marin et Melkonian 2010 -- Bathycoccaceae Marin et Melkonian 2010 -- 5.2.2.4.2 Dolichomastigales Marin et Melkonian 2010 -- Dolichomastigaceae Marin et Melkonian 2010 -- Crustomastigaceae Marin et Melkonian 2010 -- 5.2.2.4.3 Monomastigales Marin et Melkonian 2010 -- 5.2.2.5 Clade VII sensu Guillou et al. 2004 -- 5.2.2.5.1 The Picocystis Clade -- 5.2.2.6 Pycnococcaceae Guillard emend. Fawley 1999 (Clade V) -- 5.2.2.7 Nephroselmidophyceae Cavalier-Smith 1993 (Clade III) -- 5.2.2.8 Chlorodendrophyceae Massjuk 2006 (Clade IV) -- 5.2.2.9 Pedinophyceae Moestrup emend. Marin 2012 -- 5.2.2.9.1 Pedinomonadales Moestrup emend. Marin 2012 -- 5.2.2.9.2 Marsupiomonadales Marin 2011 -- 5.2.2.10 Clades VIII and IX -- 5.3 Ecology of Primitive Green Algae -- References -- Chapter 6: Typical Features of Genomes in the Mamiellophyceae -- 6.1 Introduction to Mamiellophyceae -- 6.2 Genome Characteristics of Mamiellales -- 6.2.1 The Genomes of the Mamiellales Are Small -- 6.2.2 Similar Cellular Morphologies Cloak Phylogenomic Divergence -- 6.2.3 Two Outlier Chromosomes Have Enigmatic Functionalities -- 6.3 Metabolic Processes or Life Styles Inferred from Genomes -- 6.4 Organellar Genomes -- 6.4.1 Common Features of Mamiellophyceae Organellar Genomes -- 6.4.2 Variable Features of Mamiellophyceae Organellar Genomes. , 6.4.3 Population Genomic Insights into Organelle Inheritance and Evolution -- 6.5 Metagenomics of Mamiellales -- 6.5.1 Linking Marker Gene Diversity, Physiology and Ecology -- 6.5.2 Whole Genomic Sequence from "Wild" Populations -- 6.6 Viruses -- 6.6.1 Prasinoviruses Are Diverse and Abundant -- 6.6.2 Is the Evolution of Host and Viral Genomes Driven by an Arms Race? -- 6.7 Perspectives -- References -- Chapter 7: Planktic Foraminifera -- 7.1 Introduction -- 7.1.1 What Are Foraminifera? -- 7.1.2 Evolution over Geological Timescales -- 7.1.3 Research History of Living Planktic Foraminifera: An Overview -- 7.2 Shell Morphology and Structure -- 7.2.1 Morphology-Based Classification -- 7.2.2 Shell Structure and Ontogeny -- 7.3 Horizontal and Vertical Distributions -- 7.4 Biology -- 7.4.1 Cytoplasm -- 7.4.2 Predation -- 7.4.3 Symbiosis -- 7.4.4 Reproduction and Life Cycles -- 7.5 Shell Geochemistry -- 7.5.1 Advances in Geochemistry and Paleoceanography -- 7.5.2 Oxygen and Carbon Isotopes -- 7.5.3 Trace Metals in Foraminiferal Shells -- 7.5.4 Sub-micron-Order Geochemical Analysis -- 7.6 Molecular Biology -- 7.6.1 Evolution -- 7.6.2 Origin of the Modern Planktic Foraminifera -- 7.6.3 Genetic Diversity -- 7.6.4 Geographic and Vertical Distribution of Genetic Diversity -- 7.6.5 Reassessment of Shell Morphology -- 7.7 Collection and Cultivation -- 7.7.1 Collection of Living Specimens -- 7.7.2 Preparation in the Laboratory -- 7.7.3 Maintenance of Living Specimens -- 7.7.4 Feeding and Maintenance -- 7.7.5 Sample Fixation -- 7.7.6 Advanced Systems for Ecological Study: A Flow-­Through Culture Approach -- References -- Further Reading Lists -- Chapter 8: Biology and Ecology of Radiolaria -- 8.1 Overview of Radiolarian Features -- 8.2 Acantharia -- 8.2.1 Cell Structure and Taxonomy -- 8.2.2 Reproduction and Motility. , 8.2.3 Trophic Characteristics and Biotic Interactions -- 8.2.4 Environmental Distribution -- 8.3 Taxopodia -- 8.3.1 Cell Structure and Taxonomy -- 8.3.2 Reproduction and Motility -- 8.3.3 Trophic Characteristics and Biotic Interactions -- 8.3.4 Environmental Distribution -- 8.4 Spumellaria -- 8.4.1 Cell Structure and Taxonomy -- 8.4.2 Reproduction and Motility -- 8.4.3 Trophic Characteristics and Biotic Interactions -- 8.4.4 Environmental Distributions -- 8.5 Nassellaria -- 8.5.1 Cell Structure and Taxonomy -- 8.5.2 Reproduction and Motility -- 8.5.3 Trophic Characteristics and Biotic Interactions -- 8.5.4 Environmental Distributions -- 8.6 Collodaria -- 8.6.1 Cell Structure and Taxonomy -- 8.6.2 Reproduction and Motility -- 8.6.3 Trophic Characteristics and Biotic Interactions -- 8.6.4 Environmental Distributions -- 8.7 General Ecology of Radiolaria -- 8.8 Seasonality of Polycystines in Different Regions -- 8.8.1 Upwelling Regions -- 8.8.2 Major Factors Controlling Polycystine Distributions -- 8.8.3 Contributions to Inorganic Biochemical Cycle -- 8.9 Research Perspectives on Living Radiolarians -- References -- Chapter 9: Phaeodaria: Diverse Marine Cercozoans of World-Wide Distribution -- 9.1 Introduction -- 9.1.1 What Are "Phaeodarians"? -- 9.1.2 History -- 9.2 Classification -- 9.2.1 Cercozoa -- 9.2.2 Outline of Taxonomy -- 9.3 Cell Structure -- 9.3.1 Malacoma -- 9.3.2 Scleracoma -- 9.4 Mode of Life -- 9.5 Reproduction -- 9.5.1 Cell Division -- 9.5.2 Swarmer Production -- 9.6 Trophic Interactions -- 9.6.1 Feeding -- 9.6.2 Predators and Symbiosis -- 9.7 Distribution -- 9.7.1 Global Distribution -- 9.7.2 Vertical Distribution -- 9.8 Interactions with the Environment -- 9.8.1 Restricting Factors of Phaeodarian Distribution -- 9.8.2 Biomass -- 9.8.3 Seasonality -- 9.8.4 Importance in the Matter Cycle -- 9.9 Fossil Records -- References. , Chapter 10: Ecology and Evolution of Marine Diatoms and Parmales -- 10.1 Introduction -- 10.2 Diatom -- 10.2.1 History of Study -- 10.2.2 Marine Diatom Phytoplankton Ecology -- 10.2.3 Resting Stages -- 10.2.4 Physiological Response to Stress -- 10.2.5 Iron Limitation -- 10.2.6 Genomics and the Urea Cycle -- 10.2.7 Sinking and Staying in Suspension -- 10.2.8 Life History -- 10.2.9 Diatoms and Bacteria -- 10.2.10 Toxicity -- 10.2.11 Palaeoecology -- 10.2.12 Evolution -- 10.3 Parmales -- 10.3.1 An Insight into Diatom Ancestry? -- 10.3.2 Effects of Silicon Limitation on Growth and Morphology of Parmales -- 10.3.3 Ecology -- References -- Chapter 11: Planktonic Ciliates: Diverse Ecological Function in Seawater -- 11.1 Introduction -- 11.2 Potential Growth Influencing Grazing Impact of Ciliates -- 11.3 Grazing on Picoplankton and Nanoplankton -- 11.3.1 Ciliates as Picoplankton Feeder -- 11.3.2 Ciliates as Nanoplankton Feeders -- 11.3.3 Factors to Influence Feeding Activities of Ciliates -- 11.3.4 Comparison with the Heterotrophic Dinoflagellates -- 11.4 Prey for Meso- and Macrozooplankton -- 11.5 Nutrient Regeneration -- 11.6 Specific Functions Through Prey-Predator Relationships -- 11.6.1 Role of Grazing on HAB Species -- 11.6.2 Role as Food Source for Aurelia aurita -- 11.6.3 Role as Food for Bivalves -- 11.7 Conclusion and Future Subjects -- References -- Chapter 12: Biology and Paleontology of Coccolithophores (Haptophytes) -- 12.1 Introduction -- 12.2 Life Cycle, Biomineralization and Molecular Phylogeny -- 12.3 Biogeography and Seasonality -- 12.4 Coccolithophores in the Geological Past -- 12.5 The Future of Coccolithophores -- References -- Chapter 13: Diversity and Ecology of Thraustochytrid Protists in the Marine Environment -- 13.1 Introduction -- 13.2 Taxonomy, Morphology and Molecular Phylogeny. , 13.3 Methodologies for Detecting Thraustochytrids.
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  • 2
    Keywords: Protista ; Marine algae ; Aufsatzsammlung ; Meeresbiologie ; Protozoen
    Description / Table of Contents: "This comprehensive book provides a unique overview of advance in the biology and ecology of marine protists. Nowadays marine protistology is a hot spot in science to disclose life phenomena using the latest techniques. Although many protistological textbooks deal with the cytology, genetics, ecology, and pathology of specific organisms, none keeps up with the quick pace of new discoveries on the diversity and dynamics of marine protists in general. The book Marine protists: diversity and dynamics gives an overview of current research on the phylogeny, cytology, genomics, biology, ecology, fisheries, applied sciences, geology and pathology of marine free-living and symbiotic protists. Poorly known but ecologically important protists such as labyrinthulids and apostome ciliates are also presented in detail. Special attention is paid to complex interactions between marine protists and other organisms including human beings. An understanding of the ecological roles of marine protists is essential for conservation of nature and human welfare. This book will be of great interest not only to scientists and students but also to a larger audience, to give a better understanding of protists' diverse roles in marine ecosystems."--
    Type of Medium: Book
    Pages: ix, 648 Seiten , Illustrationen, Diagramme , 235 mm x 155 mm
    ISBN: 4431551298 , 9784431551294
    DDC: 579
    Language: English
    Note: Literaturangaben
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology ecology 52 (2005), S. 0 
    ISSN: 1574-6941
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: A quantitative PCR (QPCR) assay based on the use of SYBR Green I was developed to assess the abundance of specific groups of picoeukaryotes in marine waters. Six primer sets were designed targeting four different taxonomic levels: domain (Eukaryota), division (Chlorophyta), order (Mamiellales) and genus (Bathycoccus, Micromonas, and Ostreococcus). Reaction conditions were optimized for each primer set which was validated in silico, on agarose gels, and by QPCR against a variety of target and non-target cultures. The approach was tested by estimating gene copy numbers for Micromonas, Bathycoccus, and Ostreococcus in seawater samples to which cultured cells were added in various concentrations. QPCR was then used to determine that rRNA gene (rDNA) copy number varied from one to more than 12,000 in 18 strains of phytoplankton. Finally, QPCR was applied to environmental samples from a Mediterranean Sea coastal site and the results were compared to those obtained by Fluorescent in situ hybridization (FISH). The data obtained demonstrate that Chlorophyta and more specifically Mamiellales were important in these waters, especially during the winter picoplankton bloom. The timing of major abundance peaks of the targeted species was similar by QPCR and FISH. When used in conjunction with other techniques such as FISH or gene clone libraries, QPCR appears as very promising to quickly obtain data on the ecological distribution of important phytoplankton groups. Data interpretation must take into account primer specificity and the varying rRNA gene copy number among eukaryotes.
    Type of Medium: Electronic Resource
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  • 4
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    PANGAEA
    In:  Supplement to: Biard, Tristan; Stemmann, Lars; Picheral, Marc; Mayot, Nicolas; Vandromme, Pieter; Hauss, Helena; Gorsky, G; Guidi, Lionel; Kiko, Rainer; Not, Fabrice (2016): In situ imaging reveals the biomass of giant protists in the global ocean. Nature, 532(7600), 504-507, https://doi.org/10.1038/nature17652
    Publication Date: 2023-11-09
    Description: Planktonic organisms play crucial roles in oceanic food webs and global biogeochemical cycles. Most of our knowledge about the ecological impact of large zooplankton stems from research on abundant and robust crustaceans, and in particular copepods. A number of the other organisms that comprise planktonic communities are fragile, and therefore hard to sample and quantify, meaning that their abundances and effects on oceanic ecosystems are poorly understood. Here, using data from a worldwide in situ imaging survey of plankton larger than 600 µm, we show that a substantial part of the biomass of this size fraction consists of giant protists belonging to the Rhizaria, a super-group of mostly fragile unicellular marine organisms that includes the taxa Phaeodaria and Radiolaria (for example, orders Collodaria and Acantharia). Globally, we estimate that rhizarians in the top 200 m of world oceans represent a standing stock of 0.089 Pg carbon, equivalent to 5.2% of the total oceanic biota carbon reservoir. In the vast oligotrophic intertropical open oceans, rhizarian biomass is estimated to be equivalent to that of all other mesozooplankton (plankton in the size range 0.2-20 mm). The photosymbiotic association of many rhizarians with microalgae may be an important factor in explaining their distribution. The previously overlooked importance of these giant protists across the widest ecosystem on the planet changes our understanding of marine planktonic ecosystems.
    Type: Dataset
    Format: application/zip, 3 datasets
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  • 5
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    Unknown
    PANGAEA
    In:  Supplement to: Biard, Tristan; Bigeard, Estelle; Audic, Stephane; Poulain, Julie; Gutiérrez-Rodríguez, Andrés; Stemmann, Lars; Not, Fabrice (2017): Biogeography and diversity of Collodaria (Radiolaria) in the global ocean. Nature, https://doi.org/10.1038/ismej.2017.12
    Publication Date: 2024-02-16
    Description: The present data set provides context to 653 samples (including 4 size fractions, 0.8-5 µm, 5-20 µm, 20-180 µm and 180-2000 µm) collected in the [SRF] surface water layer (ENVO:00010504) and the [DCM] deep chlorophyll maximum layer (ENVO:01000326) at 113 sampling stations during the Tara Oceans expedition. The present data set also provides links to the corresponding nucleotides data at the European Nucleotides Archive and the abundance of metabarcodes and OTUs for Rhizaria and Collodaria from the 113 sampling stations. Additional context can be found in the related publications and source data sets.
    Keywords: Fondation Tara Expeditions; FondTara; Tara_Oceans_2009-2013; Tara Oceans Expedition
    Type: Dataset
    Format: application/zip, 269.4 kBytes
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  • 6
    Publication Date: 2024-02-02
    Keywords: [day/night] [water layer with no specific feature]; [day] [integrated]; [day] [mesopelagic zone (ENVO:00000213)]; [day] [surface water layer (ENVO:00002042)]; [day] [surface water layer (ENVO:00002042)] [near; [day] [water layer with no specific feature]; [day] [water layer with no specific feature] [also; [day] [water layer with no specific feature] [near; [day] [water layer with no specific feature] [NOT; [near station 95]; [night] [water layer with no specific feature]; [night] [water layer with no specific feature] [al; [night] [water layer with no specific feature] [ne; [RVSS]; Abu Dhabi to Muscat, Stations: none; ANT-XXV/3; Arctic Net 2009 Leg 2; Ascencion to Rio de Janiero, Stations: TARA_072-076; Athens to Beyrouth, Stations: TARA_027-028; Atseranana to Mamoudzou, Stations: TARA_053-054; Bermuda to Horta, Stations: TARA_148-151; Beyrouth to Alexandria, Stations: TARA_029-030; Bizerte to Naples, Stations: TARA_014; BOUM; Buenos Aires to Ushuaia, Stations: TARA_079b-083; calculated using satellite products obtained from the Oregon University; Campaign of event; CapeTown to Ascencion, Stations: TARA_067-071; CCGS Amundsen; Chlorophyll a; CTD_10; CTD_100; CTD_102; CTD_103; CTD_104; CTD_108; CTD_109; CTD_11; CTD_110; CTD_111; CTD_112; CTD_113; CTD_115; CTD_14; CTD_18; CTD_2; CTD_21; CTD_22; CTD_25; CTD_27; CTD_3; CTD_31; CTD_32; CTD_33; CTD_34; CTD_36; CTD_37; CTD_39; CTD_4; CTD_45; CTD_47; CTD_5; CTD_50; CTD_54; CTD_6; CTD_61; CTD_64; CTD_66; CTD_7; CTD_75; CTD_78; CTD_8; CTD_83; CTD_86; CTD_89; CTD_9; CTD_90; CTD_91; CTD_92; CTD_93; CTD_94; CTD_95; CTD_96; CTD_97; CTD_98; CTD_99; CTD/Rosette; CTD/Rosette, ultra clean; CTD001; CTD002; CTD003; CTD004; CTD005; CTD006; CTD007; CTD008; CTD009; CTD010; CTD011; CTD012; CTD013; CTD014; CTD015; CTD016; CTD017; CTD018; CTD019; CTD020; CTD021; CTD022; CTD023; CTD024; CTD025; CTD026; CTD027; CTD030; CTD032; CTD033; CTD034; CTD051; CTD052; CTD053; CTD054; CTD055; CTD056; CTD057; CTD058; CTD059; CTD060; CTD061; CTD062; CTD063; CTD067; CTD 10; CTD 11; CTD 12; CTD 13; CTD-13; CTD 14; CTD 15; CTD-15; CTD 16; CTD-16; CTD 17; CTD-17; CTD 18; CTD 19; CTD-19; CTD 20; CTD-20; CTD 22; CTD 23; CTD-23; CTD 24; CTD-24; CTD 25; CTD 26; CTD-26; CTD 27; CTD 28; CTD-28; CTD 29; CTD 3; CTD 30; CTD-30; CTD 31; CTD 32; CTD 33; CTD 34; CTD 35; CTD-35; CTD 36; CTD-38; CTD 4; CTD-40; CTD-41; CTD-42; CTD 43; CTD-43; CTD 44; CTD-44; CTD-46; CTD 47; CTD 48; CTD-48; CTD-49; CTD 5; CTD 51; CTD-51; CTD-52; CTD 53; CTD-53; CTD 54; CTD-55; CTD 56; CTD-56; CTD 57; CTD 58; CTD-58; CTD 59; CTD-59; CTD 6; CTD 60; CTD-60; CTD 61; CTD 62; CTD-62; CTD 63; CTD 64; CTD 65; CTD-65; CTD 66; CTD 67; CTD-67; CTD-69; CTD 7; CTD-70; CTD-71; CTD-72; CTD-73; CTD-74; CTD-76; CTD-77; CTD-79; CTD 8; CTD-80; CTD-82; CTD-84; CTD-85; CTD-87; CTD-88; CTD 9; CTD-RO; CTD-UC; Date/Time of event; determined from sea surface chlorophyll a; Diffuse attenuation coefficient at 490 nm; Dubrovnik to Athens, Stations: TARA_025-026; Dudinka to Pevek, Stations: TARA_182-192; Easter Island to Guayaquil, Stations: TARA_098-102; Environmental feature; Event label; Guayaquil to Puerto Ayora, Stations: TARA_103-106; Guayaquil to Totegegie, Stations: TARA_110-113; Honolulu to San Diego, Stations: TARA_131-135; Horta to La Coruna, Stations: TARA_152-154; Ilulissat to Québec, Stations: TARA_208-210; IORVL/MALINA; L Atalante; LATALANTE_20080619T0813Z_001_CAST; LATALANTE_20080621T0016Z_002_CAST; LATALANTE_20080621T0354Z_003_CAST; LATALANTE_20080621T1039Z_004_CAST; LATALANTE_20080621T1941Z_005_CAST; LATALANTE_20080621T2256Z_006_CAST; LATALANTE_20080622T0551Z_007_CAST; LATALANTE_20080622T1347Z_008_CAST; LATALANTE_20080622T1656Z_009_CAST; LATALANTE_20080622T2335Z_010_CAST; LATALANTE_20080623T0753Z_011_CAST; LATALANTE_20080623T1124Z_012_CAST; LATALANTE_20080624T1216Z_016_CAST; LATALANTE_20080624T2317Z_017_CAST; LATALANTE_20080625T0228Z_018_CAST; LATALANTE_20080625T1527Z_019_CAST; LATALANTE_20080625T1643Z_020_CAST; LATALANTE_20080625T1740Z_021_CAST; LATALANTE_20080625T1842Z_022_CAST; LATALANTE_20080625T2001Z_023_CAST; LATALANTE_20080625T2107Z_024_CAST; LATALANTE_20080625T2209Z_025_CAST; LATALANTE_20080625T2333Z_026_CAST; LATALANTE_20080626T0031Z_027_CAST; LATALANTE_20080626T0130Z_028_CAST; LATALANTE_20080626T0244Z_029_CAST; LATALANTE_20080626T0339Z_030_CAST; LATALANTE_20080626T0430Z_031_CAST; LATALANTE_20080626T0526Z_032_CAST; LATALANTE_20080626T0629Z_033_CAST; LATALANTE_20080626T0734Z_034_CAST; LATALANTE_20080626T0906Z_035_CAST; LATALANTE_20080626T1003Z_036_CAST; LATALANTE_20080626T1104Z_037_CAST; LATALANTE_20080626T1202Z_038_CAST; LATALANTE_20080626T1310Z_039_CAST; LATALANTE_20080626T2200Z_040_CAST; LATALANTE_20080626T2252Z_041_CAST; LATALANTE_20080627T0025Z_042_CAST; LATALANTE_20080627T0322Z_043_CAST; LATALANTE_20080627T0612Z_044_CAST; LATALANTE_20080627T0941Z_047_CAST; LATALANTE_20080627T1215Z_048_CAST; LATALANTE_20080627T1505Z_049_CAST; LATALANTE_20080627T1804Z_050_CAST; LATALANTE_20080627T2102Z_051_CAST; LATALANTE_20080628T0002Z_052_CAST; LATALANTE_20080628T0304Z_053_CAST; LATALANTE_20080628T0603Z_054_CAST; LATALANTE_20080628T0914Z_055_CAST; LATALANTE_20080628T1210Z_056_CAST; LATALANTE_20080628T1459Z_057_CAST; LATALANTE_20080628T1758Z_058_CAST; LATALANTE_20080628T2053Z_059_CAST; LATALANTE_20080628T2212Z_060_CAST; LATALANTE_20080628T2315Z_061_CAST; LATALANTE_20080629T0031Z_062_CAST; LATALANTE_20080629T0155Z_063_CAST; LATALANTE_20080629T0302Z_064_CAST; LATALANTE_20080629T0604Z_065_CAST; LATALANTE_20080629T0855Z_066_CAST; LATALANTE_20080629T1512Z_068_CAST; LATALANTE_20080629T1802Z_069_CAST; LATALANTE_20080629T2120Z_070_CAST; LATALANTE_20080629T2303Z_071_CAST; LATALANTE_20080703T1125Z_072_CAST; LATALANTE_20080703T1301Z_073_CAST; LATALANTE_20080703T1359Z_074_CAST; LATALANTE_20080703T1459Z_075_CAST; LATALANTE_20080703T1553Z_076_CAST; LATALANTE_20080703T1648Z_077_CAST; LATALANTE_20080703T1739Z_078_CAST; LATALANTE_20080703T1840Z_079_CAST; LATALANTE_20080703T1949Z_080_CAST; LATALANTE_20080703T2057Z_081_CAST; LATALANTE_20080703T2303Z_082_CAST; LATALANTE_20080704T0000Z_083_CAST; LATALANTE_20080704T0120Z_084_CAST; LATALANTE_20080704T0402Z_085_CAST; LATALANTE_20080704T0703Z_088_CAST; LATALANTE_20080704T1305Z_090_CAST; LATALANTE_20080704T1603Z_091_CAST; LATALANTE_20080704T1854Z_092_CAST; LATALANTE_20080704T2210Z_093_CAST; LATALANTE_20080705T0103Z_094_CAST; LATALANTE_20080705T0401Z_095_CAST; LATALANTE_20080705T0701Z_096_CAST; LATALANTE_20080705T1012Z_097_CAST; LATALANTE_20080705T1305Z_098_CAST; LATALANTE_20080705T1645Z_099_CAST; LATALANTE_20080705T1901Z_100_CAST; LATALANTE_20080705T2159Z_101_CAST; LATALANTE_20080705T2315Z_102_CAST; LATALANTE_20080706T0016Z_103_CAST; LATALANTE_20080706T0138Z_104_CAST; LATALANTE_20080706T0400Z_105_CAST; LATALANTE_20080706T0441Z_106_CAST; LATALANTE_20080706T0703Z_107_CAST; LATALANTE_20080706T0830Z_108_CAST; LATALANTE_20080706T1007Z_109_CAST; LATALANTE_20080706T1257Z_110_CAST; LATALANTE_20080706T1602Z_111_CAST; LATALANTE_20080706T1919Z_112_CAST; LATALANTE_20080706T2204Z_113_CAST; LATALANTE_20080706T2341Z_114_CAST; LATALANTE_20080707T1008Z_115_CAST; LATALANTE_20080707T1916Z_216_CAST; LATALANTE_20080707T2042Z_116_CAST; LATALANTE_20080708T0017Z_117_CAST; LATALANTE_20080708T0805Z_118_CAST; LATALANTE_20080708T1559Z_119_CAST; LATALANTE_20080708T1742Z_120_CAST; LATALANTE_20080709T0103Z_121_CAST; LATALANTE_20080709T1056Z_122_CAST; LATALANTE_20080709T1235Z_123_CAST; LATALANTE_20080709T1900Z_124_CAST; LATALANTE_20080710T0826Z_125_CAST; LATALANTE_20080710T1001Z_126_CAST; LATALANTE_20080710T1613Z_127_CAST; LATALANTE_20080711T0218Z_128_CAST; LATALANTE_20080711T1120Z_130_CAST; LATALANTE_20080712T1051Z_131_CAST; LATALANTE_20080712T1209Z_132_CAST; LATALANTE_20080712T1307Z_133_CAST; LATALANTE_20080712T1405Z_134_CAST; LATALANTE_20080712T1530Z_135_CAST; LATALANTE_20080712T1626Z_136_CAST; LATALANTE_20080712T1721Z_137_CAST; LATALANTE_20080712T1840Z_138_CAST; LATALANTE_20080712T1944Z_139_CAST; LATALANTE_20080712T2045Z_140_CAST; LATALANTE_20080712T2208Z_141_CAST;
    Type: Dataset
    Format: text/tab-separated-values, 6773 data points
    Location Call Number Limitation Availability
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  • 7
    Publication Date: 2024-02-02
    Keywords: [day/night] [water layer with no specific feature]; [day] [integrated]; [day] [mesopelagic zone (ENVO:00000213)]; [day] [surface water layer (ENVO:00002042)]; [day] [surface water layer (ENVO:00002042)] [near; [day] [water layer with no specific feature]; [day] [water layer with no specific feature] [also; [day] [water layer with no specific feature] [near; [day] [water layer with no specific feature] [NOT; [near station 95]; [night] [water layer with no specific feature]; [night] [water layer with no specific feature] [al; [night] [water layer with no specific feature] [ne; [RVSS]; Abu Dhabi to Muscat, Stations: none; Acantharia, biomass as carbon; ANT-XXV/3; Arctic Net 2009 Leg 2; Ascencion to Rio de Janiero, Stations: TARA_072-076; Athens to Beyrouth, Stations: TARA_027-028; Atseranana to Mamoudzou, Stations: TARA_053-054; Bermuda to Horta, Stations: TARA_148-151; Beyrouth to Alexandria, Stations: TARA_029-030; Bizerte to Naples, Stations: TARA_014; BOUM; Buenos Aires to Ushuaia, Stations: TARA_079b-083; Campaign of event; CapeTown to Ascencion, Stations: TARA_067-071; CCGS Amundsen; Collodaria, biomass as carbon; converted to carbon from individual biovolume measurements (Biard et al. 2016); CTD_10; CTD_100; CTD_102; CTD_103; CTD_104; CTD_108; CTD_109; CTD_11; CTD_110; CTD_111; CTD_112; CTD_113; CTD_115; CTD_14; CTD_18; CTD_2; CTD_21; CTD_22; CTD_25; CTD_27; CTD_3; CTD_31; CTD_32; CTD_33; CTD_34; CTD_36; CTD_37; CTD_39; CTD_4; CTD_45; CTD_47; CTD_5; CTD_50; CTD_54; CTD_6; CTD_61; CTD_64; CTD_66; CTD_7; CTD_75; CTD_78; CTD_8; CTD_83; CTD_86; CTD_89; CTD_9; CTD_90; CTD_91; CTD_92; CTD_93; CTD_94; CTD_95; CTD_96; CTD_97; CTD_98; CTD_99; CTD/Rosette; CTD/Rosette, ultra clean; CTD001; CTD002; CTD003; CTD004; CTD005; CTD006; CTD007; CTD008; CTD009; CTD010; CTD011; CTD012; CTD013; CTD014; CTD015; CTD016; CTD017; CTD018; CTD019; CTD020; CTD021; CTD022; CTD023; CTD024; CTD025; CTD026; CTD027; CTD030; CTD032; CTD033; CTD034; CTD051; CTD052; CTD053; CTD054; CTD055; CTD056; CTD057; CTD058; CTD059; CTD060; CTD061; CTD062; CTD063; CTD067; CTD 10; CTD 11; CTD 12; CTD 13; CTD-13; CTD 14; CTD 15; CTD-15; CTD 16; CTD-16; CTD 17; CTD-17; CTD 18; CTD 19; CTD-19; CTD 20; CTD-20; CTD 22; CTD 23; CTD-23; CTD 24; CTD-24; CTD 25; CTD 26; CTD-26; CTD 27; CTD 28; CTD-28; CTD 29; CTD 3; CTD 30; CTD-30; CTD 31; CTD 32; CTD 33; CTD 34; CTD 35; CTD-35; CTD 36; CTD-38; CTD 4; CTD-40; CTD-41; CTD-42; CTD 43; CTD-43; CTD 44; CTD-44; CTD-46; CTD 47; CTD 48; CTD-48; CTD-49; CTD 5; CTD 51; CTD-51; CTD-52; CTD 53; CTD-53; CTD 54; CTD-55; CTD 56; CTD-56; CTD 57; CTD 58; CTD-58; CTD 59; CTD-59; CTD 6; CTD 60; CTD-60; CTD 61; CTD 62; CTD-62; CTD 63; CTD 64; CTD 65; CTD-65; CTD 66; CTD 67; CTD-67; CTD-69; CTD 7; CTD-70; CTD-71; CTD-72; CTD-73; CTD-74; CTD-76; CTD-77; CTD-79; CTD 8; CTD-80; CTD-82; CTD-84; CTD-85; CTD-87; CTD-88; CTD 9; CTD-RO; CTD-UC; Date/Time of event; Depth, bottom/max; Depth, nominal; Depth, top/min; Dubrovnik to Athens, Stations: TARA_025-026; Dudinka to Pevek, Stations: TARA_182-192; Easter Island to Guayaquil, Stations: TARA_098-102; Event label; Guayaquil to Puerto Ayora, Stations: TARA_103-106; Guayaquil to Totegegie, Stations: TARA_110-113; Honolulu to San Diego, Stations: TARA_131-135; Horta to La Coruna, Stations: TARA_152-154; Ilulissat to Québec, Stations: TARA_208-210; IORVL/MALINA; L Atalante; LATALANTE_20080619T0813Z_001_CAST; LATALANTE_20080621T0016Z_002_CAST; LATALANTE_20080621T0354Z_003_CAST; LATALANTE_20080621T1039Z_004_CAST; LATALANTE_20080621T1941Z_005_CAST; LATALANTE_20080621T2256Z_006_CAST; LATALANTE_20080622T0551Z_007_CAST; LATALANTE_20080622T1347Z_008_CAST; LATALANTE_20080622T1656Z_009_CAST; LATALANTE_20080622T2335Z_010_CAST; LATALANTE_20080623T0753Z_011_CAST; LATALANTE_20080623T1124Z_012_CAST; LATALANTE_20080624T1216Z_016_CAST; LATALANTE_20080624T2317Z_017_CAST; LATALANTE_20080625T0228Z_018_CAST; LATALANTE_20080625T1527Z_019_CAST; LATALANTE_20080625T1643Z_020_CAST; LATALANTE_20080625T1740Z_021_CAST; LATALANTE_20080625T1842Z_022_CAST; LATALANTE_20080625T2001Z_023_CAST; LATALANTE_20080625T2107Z_024_CAST; LATALANTE_20080625T2209Z_025_CAST; LATALANTE_20080625T2333Z_026_CAST; LATALANTE_20080626T0031Z_027_CAST; LATALANTE_20080626T0130Z_028_CAST; LATALANTE_20080626T0244Z_029_CAST; LATALANTE_20080626T0339Z_030_CAST; LATALANTE_20080626T0430Z_031_CAST; LATALANTE_20080626T0526Z_032_CAST; LATALANTE_20080626T0629Z_033_CAST; LATALANTE_20080626T0734Z_034_CAST; LATALANTE_20080626T0906Z_035_CAST; LATALANTE_20080626T1003Z_036_CAST; LATALANTE_20080626T1104Z_037_CAST; LATALANTE_20080626T1202Z_038_CAST; LATALANTE_20080626T1310Z_039_CAST; LATALANTE_20080626T2200Z_040_CAST; LATALANTE_20080626T2252Z_041_CAST; LATALANTE_20080627T0025Z_042_CAST; LATALANTE_20080627T0322Z_043_CAST; LATALANTE_20080627T0612Z_044_CAST; LATALANTE_20080627T0941Z_047_CAST; LATALANTE_20080627T1215Z_048_CAST; LATALANTE_20080627T1505Z_049_CAST; LATALANTE_20080627T1804Z_050_CAST; LATALANTE_20080627T2102Z_051_CAST; LATALANTE_20080628T0002Z_052_CAST; LATALANTE_20080628T0304Z_053_CAST; LATALANTE_20080628T0603Z_054_CAST; LATALANTE_20080628T0914Z_055_CAST; LATALANTE_20080628T1210Z_056_CAST; LATALANTE_20080628T1459Z_057_CAST; LATALANTE_20080628T1758Z_058_CAST; LATALANTE_20080628T2053Z_059_CAST; LATALANTE_20080628T2212Z_060_CAST; LATALANTE_20080628T2315Z_061_CAST; LATALANTE_20080629T0031Z_062_CAST; LATALANTE_20080629T0155Z_063_CAST; LATALANTE_20080629T0302Z_064_CAST; LATALANTE_20080629T0604Z_065_CAST; LATALANTE_20080629T0855Z_066_CAST; LATALANTE_20080629T1512Z_068_CAST; LATALANTE_20080629T1802Z_069_CAST; LATALANTE_20080629T2120Z_070_CAST; LATALANTE_20080629T2303Z_071_CAST; LATALANTE_20080703T1125Z_072_CAST; LATALANTE_20080703T1301Z_073_CAST; LATALANTE_20080703T1359Z_074_CAST; LATALANTE_20080703T1459Z_075_CAST; LATALANTE_20080703T1553Z_076_CAST; LATALANTE_20080703T1648Z_077_CAST; LATALANTE_20080703T1739Z_078_CAST; LATALANTE_20080703T1840Z_079_CAST; LATALANTE_20080703T1949Z_080_CAST; LATALANTE_20080703T2057Z_081_CAST; LATALANTE_20080703T2303Z_082_CAST; LATALANTE_20080704T0000Z_083_CAST; LATALANTE_20080704T0120Z_084_CAST; LATALANTE_20080704T0402Z_085_CAST; LATALANTE_20080704T0703Z_088_CAST; LATALANTE_20080704T1305Z_090_CAST; LATALANTE_20080704T1603Z_091_CAST; LATALANTE_20080704T1854Z_092_CAST; LATALANTE_20080704T2210Z_093_CAST; LATALANTE_20080705T0103Z_094_CAST; LATALANTE_20080705T0401Z_095_CAST; LATALANTE_20080705T0701Z_096_CAST; LATALANTE_20080705T1012Z_097_CAST; LATALANTE_20080705T1305Z_098_CAST; LATALANTE_20080705T1645Z_099_CAST; LATALANTE_20080705T1901Z_100_CAST; LATALANTE_20080705T2159Z_101_CAST; LATALANTE_20080705T2315Z_102_CAST; LATALANTE_20080706T0016Z_103_CAST; LATALANTE_20080706T0138Z_104_CAST; LATALANTE_20080706T0400Z_105_CAST; LATALANTE_20080706T0441Z_106_CAST; LATALANTE_20080706T0703Z_107_CAST; LATALANTE_20080706T0830Z_108_CAST; LATALANTE_20080706T1007Z_109_CAST; LATALANTE_20080706T1257Z_110_CAST; LATALANTE_20080706T1602Z_111_CAST; LATALANTE_20080706T1919Z_112_CAST; LATALANTE_20080706T2204Z_113_CAST; LATALANTE_20080706T2341Z_114_CAST; LATALANTE_20080707T1008Z_115_CAST; LATALANTE_20080707T1916Z_216_CAST; LATALANTE_20080707T2042Z_116_CAST; LATALANTE_20080708T0017Z_117_CAST; LATALANTE_20080708T0805Z_118_CAST; LATALANTE_20080708T1559Z_119_CAST; LATALANTE_20080708T1742Z_120_CAST; LATALANTE_20080709T0103Z_121_CAST; LATALANTE_20080709T1056Z_122_CAST; LATALANTE_20080709T1235Z_123_CAST; LATALANTE_20080709T1900Z_124_CAST; LATALANTE_20080710T0826Z_125_CAST; LATALANTE_20080710T1001Z_126_CAST; LATALANTE_20080710T1613Z_127_CAST; LATALANTE_20080711T0218Z_128_CAST; LATALANTE_20080711T1120Z_130_CAST; LATALANTE_20080712T1051Z_131_CAST; LATALANTE_20080712T1209Z_132_CAST; LATALANTE_20080712T1307Z_133_CAST; LATALANTE_20080712T1405Z_134_CAST; LATALANTE_20080712T1530Z_135_CAST; LATALANTE_20080712T1626Z_136_CAST; LATALANTE_20080712T1721Z_137_CAST; LATALANTE_20080712T1840Z_138_CAST; LATALANTE_20080712T1944Z_139_CAST; LATALANTE_20080712T2045Z_140_CAST; LATALANTE_20080712T2208Z_141_CAST;
    Type: Dataset
    Format: text/tab-separated-values, 24573 data points
    Location Call Number Limitation Availability
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  • 8
    Publication Date: 2024-02-02
    Keywords: [day/night] [deep chlorophyll maximum layer (ENVO:; [day/night] [mesopelagic zone (ENVO:00000213)]; [day/night] [water layer with no specific feature]; [day] [200 m]; [day] [deep chlorophyll maximum layer (ENVO:010003; [day] [epipelagic mixed layer (ENVO:01000061)]; [day] [integrated]; [day] [mesopelagic zone (ENVO:00000213)]; [day] [mesopelagic zone (ENVO:00000213)] [also lab; [day] [surface water layer (ENVO:00002042)]; [day] [surface water layer (ENVO:00002042)] [near; [day] [water layer with no specific feature]; [day] [water layer with no specific feature] [also; [day] [water layer with no specific feature] [Lago; [day] [water layer with no specific feature] [near; [day] [water layer with no specific feature] [NOT; [near station 95]; [night] [deep chlorophyll maximum layer (ENVO:0100; [night] [mesopelagic zone (ENVO:00000213)]; [night] [surface water layer (ENVO:00002042)] [nea; [night] [water layer with no specific feature]; [night] [water layer with no specific feature] [al; [night] [water layer with no specific feature] [ne; [RVSS]; Abu Dhabi to Muscat, Stations: none; Acantharia; ANT-XXV/3; Arctic Net 2009 Leg 2; Ascencion to Rio de Janiero, Stations: TARA_072-076; Athens to Beyrouth, Stations: TARA_027-028; Atseranana to Mamoudzou, Stations: TARA_053-054; Bermuda to Horta, Stations: TARA_148-151; Beyrouth to Alexandria, Stations: TARA_029-030; Bizerte to Naples, Stations: TARA_014; BOUM; Buenos Aires to Ushuaia, Stations: TARA_079b-083; Campaign of event; CapeTown to Ascencion, Stations: TARA_067-071; CCGS Amundsen; Collodaria; CTD_10; CTD_100; CTD_102; CTD_103; CTD_104; CTD_108; CTD_109; CTD_11; CTD_110; CTD_111; CTD_112; CTD_113; CTD_115; CTD_14; CTD_18; CTD_2; CTD_21; CTD_22; CTD_25; CTD_27; CTD_3; CTD_31; CTD_32; CTD_33; CTD_34; CTD_36; CTD_37; CTD_39; CTD_4; CTD_45; CTD_47; CTD_5; CTD_50; CTD_54; CTD_6; CTD_61; CTD_64; CTD_66; CTD_7; CTD_75; CTD_78; CTD_8; CTD_83; CTD_86; CTD_89; CTD_9; CTD_90; CTD_91; CTD_92; CTD_93; CTD_94; CTD_95; CTD_96; CTD_97; CTD_98; CTD_99; CTD/Rosette; CTD/Rosette, ultra clean; CTD001; CTD002; CTD003; CTD004; CTD005; CTD006; CTD007; CTD008; CTD009; CTD010; CTD011; CTD012; CTD013; CTD014; CTD015; CTD016; CTD017; CTD018; CTD019; CTD020; CTD021; CTD022; CTD023; CTD024; CTD025; CTD026; CTD027; CTD030; CTD032; CTD033; CTD034; CTD051; CTD052; CTD053; CTD054; CTD055; CTD056; CTD057; CTD058; CTD059; CTD060; CTD061; CTD062; CTD063; CTD067; CTD 10; CTD 11; CTD 12; CTD 13; CTD-13; CTD 14; CTD 15; CTD-15; CTD 16; CTD-16; CTD 17; CTD-17; CTD 18; CTD 19; CTD-19; CTD 20; CTD-20; CTD 22; CTD 23; CTD-23; CTD 24; CTD-24; CTD 25; CTD 26; CTD-26; CTD 27; CTD 28; CTD-28; CTD 29; CTD 3; CTD 30; CTD-30; CTD 31; CTD 32; CTD 33; CTD 34; CTD 35; CTD-35; CTD 36; CTD-38; CTD 4; CTD-40; CTD-41; CTD-42; CTD 43; CTD-43; CTD 44; CTD-44; CTD-46; CTD 47; CTD 48; CTD-48; CTD-49; CTD 5; CTD 51; CTD-51; CTD-52; CTD 53; CTD-53; CTD 54; CTD-55; CTD 56; CTD-56; CTD 57; CTD 58; CTD-58; CTD 59; CTD-59; CTD 6; CTD 60; CTD-60; CTD 61; CTD 62; CTD-62; CTD 63; CTD 64; CTD 65; CTD-65; CTD 66; CTD 67; CTD-67; CTD-69; CTD 7; CTD-70; CTD-71; CTD-72; CTD-73; CTD-74; CTD-76; CTD-77; CTD-79; CTD 8; CTD-80; CTD-82; CTD-84; CTD-85; CTD-87; CTD-88; CTD 9; CTD-RO; CTD-UC; Date/Time of event; Depth, bottom/max; Depth, top/min; DEPTH, water; Device type; Dubrovnik to Athens, Stations: TARA_025-026; Dudinka to Pevek, Stations: TARA_182-192; Easter Island to Guayaquil, Stations: TARA_098-102; Event label; File name; Guayaquil to Puerto Ayora, Stations: TARA_103-106; Guayaquil to Totegegie, Stations: TARA_110-113; Honolulu to San Diego, Stations: TARA_131-135; Horta to La Coruna, Stations: TARA_152-154; Ilulissat to Québec, Stations: TARA_208-210; IORVL/MALINA; L Atalante; LATALANTE_20080619T0813Z_001_CAST; LATALANTE_20080621T0016Z_002_CAST; LATALANTE_20080621T0354Z_003_CAST; LATALANTE_20080621T1039Z_004_CAST; LATALANTE_20080621T1941Z_005_CAST; LATALANTE_20080621T2256Z_006_CAST; LATALANTE_20080622T0551Z_007_CAST; LATALANTE_20080622T1347Z_008_CAST; LATALANTE_20080622T1656Z_009_CAST; LATALANTE_20080622T2335Z_010_CAST; LATALANTE_20080623T0753Z_011_CAST; LATALANTE_20080623T1124Z_012_CAST; LATALANTE_20080624T1216Z_016_CAST; LATALANTE_20080624T2317Z_017_CAST; LATALANTE_20080625T0228Z_018_CAST; LATALANTE_20080625T1527Z_019_CAST; LATALANTE_20080625T1643Z_020_CAST; LATALANTE_20080625T1740Z_021_CAST; LATALANTE_20080625T1842Z_022_CAST; LATALANTE_20080625T2001Z_023_CAST; LATALANTE_20080625T2107Z_024_CAST; LATALANTE_20080625T2209Z_025_CAST; LATALANTE_20080625T2333Z_026_CAST; LATALANTE_20080626T0031Z_027_CAST; LATALANTE_20080626T0130Z_028_CAST; LATALANTE_20080626T0244Z_029_CAST; LATALANTE_20080626T0339Z_030_CAST; LATALANTE_20080626T0430Z_031_CAST; LATALANTE_20080626T0526Z_032_CAST; LATALANTE_20080626T0629Z_033_CAST; LATALANTE_20080626T0734Z_034_CAST; LATALANTE_20080626T0906Z_035_CAST; LATALANTE_20080626T1003Z_036_CAST; LATALANTE_20080626T1104Z_037_CAST; LATALANTE_20080626T1202Z_038_CAST; LATALANTE_20080626T1310Z_039_CAST; LATALANTE_20080626T2200Z_040_CAST; LATALANTE_20080626T2252Z_041_CAST; LATALANTE_20080627T0025Z_042_CAST; LATALANTE_20080627T0322Z_043_CAST; LATALANTE_20080627T0612Z_044_CAST; LATALANTE_20080627T0941Z_047_CAST; LATALANTE_20080627T1215Z_048_CAST; LATALANTE_20080627T1505Z_049_CAST; LATALANTE_20080627T1804Z_050_CAST; LATALANTE_20080627T2102Z_051_CAST; LATALANTE_20080628T0002Z_052_CAST; LATALANTE_20080628T0304Z_053_CAST; LATALANTE_20080628T0603Z_054_CAST; LATALANTE_20080628T0914Z_055_CAST; LATALANTE_20080628T1210Z_056_CAST; LATALANTE_20080628T1459Z_057_CAST; LATALANTE_20080628T1758Z_058_CAST; LATALANTE_20080628T2053Z_059_CAST; LATALANTE_20080628T2212Z_060_CAST; LATALANTE_20080628T2315Z_061_CAST; LATALANTE_20080629T0031Z_062_CAST; LATALANTE_20080629T0155Z_063_CAST; LATALANTE_20080629T0302Z_064_CAST; LATALANTE_20080629T0604Z_065_CAST; LATALANTE_20080629T0855Z_066_CAST; LATALANTE_20080629T1512Z_068_CAST; LATALANTE_20080629T1802Z_069_CAST; LATALANTE_20080629T2120Z_070_CAST; LATALANTE_20080629T2303Z_071_CAST; LATALANTE_20080703T1125Z_072_CAST; LATALANTE_20080703T1301Z_073_CAST; LATALANTE_20080703T1359Z_074_CAST; LATALANTE_20080703T1459Z_075_CAST; LATALANTE_20080703T1553Z_076_CAST; LATALANTE_20080703T1648Z_077_CAST; LATALANTE_20080703T1739Z_078_CAST; LATALANTE_20080703T1840Z_079_CAST; LATALANTE_20080703T1949Z_080_CAST; LATALANTE_20080703T2057Z_081_CAST; LATALANTE_20080703T2303Z_082_CAST; LATALANTE_20080704T0000Z_083_CAST; LATALANTE_20080704T0120Z_084_CAST; LATALANTE_20080704T0402Z_085_CAST; LATALANTE_20080704T0703Z_088_CAST; LATALANTE_20080704T1305Z_090_CAST; LATALANTE_20080704T1603Z_091_CAST; LATALANTE_20080704T1854Z_092_CAST; LATALANTE_20080704T2210Z_093_CAST; LATALANTE_20080705T0103Z_094_CAST; LATALANTE_20080705T0401Z_095_CAST; LATALANTE_20080705T0701Z_096_CAST; LATALANTE_20080705T1012Z_097_CAST; LATALANTE_20080705T1305Z_098_CAST; LATALANTE_20080705T1645Z_099_CAST; LATALANTE_20080705T1901Z_100_CAST; LATALANTE_20080705T2159Z_101_CAST; LATALANTE_20080705T2315Z_102_CAST; LATALANTE_20080706T0016Z_103_CAST; LATALANTE_20080706T0138Z_104_CAST; LATALANTE_20080706T0400Z_105_CAST; LATALANTE_20080706T0441Z_106_CAST; LATALANTE_20080706T0703Z_107_CAST; LATALANTE_20080706T0830Z_108_CAST; LATALANTE_20080706T1007Z_109_CAST; LATALANTE_20080706T1257Z_110_CAST; LATALANTE_20080706T1602Z_111_CAST; LATALANTE_20080706T1919Z_112_CAST; LATALANTE_20080706T2204Z_113_CAST; LATALANTE_20080706T2341Z_114_CAST; LATALANTE_20080707T1008Z_115_CAST; LATALANTE_20080707T1916Z_216_CAST; LATALANTE_20080707T2042Z_116_CAST; LATALANTE_20080708T0017Z_117_CAST; LATALANTE_20080708T0805Z_118_CAST; LATALANTE_20080708T1559Z_119_CAST; LATALANTE_20080708T1742Z_120_CAST; LATALANTE_20080709T0103Z_121_CAST; LATALANTE_20080709T1056Z_122_CAST; LATALANTE_20080709T1235Z_123_CAST; LATALANTE_20080709T1900Z_124_CAST; LATALANTE_20080710T0826Z_125_CAST; LATALANTE_20080710T1001Z_126_CAST; LATALANTE_20080710T1613Z_127_CAST; LATALANTE_20080711T0218Z_128_CAST; LATALANTE_20080711T1120Z_130_CAST; LATALANTE_20080712T1051Z_131_CAST;
    Type: Dataset
    Format: text/tab-separated-values, 1145392 data points
    Location Call Number Limitation Availability
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  • 9
    Publication Date: 2019-09-23
    Description: Planktonic organisms play crucial roles in oceanic food webs and global biogeochemical cycles(1,2). Most of our knowledge about the ecological impact of large zooplankton stems from research on abundant and robust crustaceans, and in particular copepods(3,4). A number of the other organisms that comprise planktonic communities are fragile, and therefore hard to sample and quantify, meaning that their abundances and effects on oceanic ecosystems are poorly understood. Here, using data from a worldwide in situ imaging survey of plankton larger than 600 mu m, we show that a substantial part of the biomass of this size fraction consists of giant protists belonging to the Rhizaria, a super-group of mostly fragile unicellular marine organisms that includes the taxa Phaeodaria and Radiolaria ( for example, orders Collodaria and Acantharia). Globally, we estimate that rhizarians in the top 200 m of world oceans represent a standing stock of 0.089 Pg carbon, equivalent to 5.2% of the total oceanic biota carbon reservoir(5). In the vast oligotrophic intertropical open oceans, rhizarian biomass is estimated to be equivalent to that of all other mesozooplankton ( plankton in the size range 0.2-20 mm). The photosymbiotic association of many rhizarians with microalgae may be an important factor in explaining their distribution. The previously overlooked importance of these giant protists across the widest ecosystem on the planet(6) changes our understanding of marine planktonic ecosystems.
    Type: Article , PeerReviewed
    Format: text
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  • 10
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    Wiley
    In:  In: Microbial Ecology of the Oceans. Wiley, Hoboken, NJ, USA, pp. 159-205. 2. ed. ISBN 9780470043448
    Publication Date: 2019-09-23
    Type: Book chapter , NonPeerReviewed
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