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  • Data  (13)
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  • 1
    Publication Date: 2023-03-16
    Description: Gene expression profile from gill and muscle tissue samples. Juvenile abalones were exposed to a temperature ramp (+3 °C day−1) under hypoxia (50% air saturation) and hypercapnia (~1000 μatm pCO2), both individually and in combination. Experiments are denoted as control (warming under normoxic normocapnia), hypoxia (warming under hypoxic normocapnia), hypercapnia (warming under normoxic hypercapnia, and combined (warming under hypoxic hypercapnia). The table is arranged to be used with the R package MCMC.qPCR (Matz et al., 2013).
    Type: Dataset
    Format: application/zip, 31.3 kBytes
    Location Call Number Limitation Availability
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  • 2
    Publication Date: 2023-04-01
    Description: We applied metagenomic shotgun sequencing to a sedimentary ancient DNA (sedaDNA) record from the North Pacific (off Kamchatka) covering the last 20,000 years to trace temporal changes in ecosystem composition and food webs. This dataset contains count data before re-sampling for (1) phototrophic bacterial and eukaryotic pelagic families, (2) and eukaryotic benthic families, and (3) a list of families, their grouping into habitat (pelagic/benthic) and trophic status (phototrophic/heterotrophic), the taxonomic group to which the family belongs, the resampled number of read counts used for the formal analysis, links (edges) in the pelagic network, and Spearman correlation coefficients (ρ〉0.2) and Benjamini-Hochberg adjusted p-values between families and environmental variables (SSTs and IP25). Associated sequencing data, on which the taxonomic classifications are based on, can be found at the European Nucleotide Archive (ENA) under BIOPROJECT: PRJEB46821.
    Keywords: AWI_Envi; Polar Terrestrial Environmental Systems @ AWI
    Type: Dataset
    Format: application/zip, 3 datasets
    Location Call Number Limitation Availability
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  • 3
    Publication Date: 2023-06-27
    Keywords: Algae & Protists; AWI_Envi; Calculated; Coefficient; Counts; Ecology & Environment; Family; Habitat; IP25 adjusted p-value; IP25 Spearman's rho; KALMAR II; Kronotsky Peninsula; Number; PC; Piston corer; Polar Terrestrial Environmental Systems @ AWI; p-value; SO201/2; SO201-2-12KL; Sonne; SST adjusted p-value; SST Spearman's rho; Taxon/taxa
    Type: Dataset
    Format: text/tab-separated-values, 1277 data points
    Location Call Number Limitation Availability
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  • 4
    Publication Date: 2023-08-02
    Keywords: Acanthasteridae; Acroporidae; Actiniidae; Agaraceae; AGE; Aglajidae; Aiptasiidae; Alariaceae; Alcyoniidae; Algae & Protists; Allocrangonyctidae; Ammotheidae; Ampullariidae; Aplysiidae; Aporocotylidae; Arcidae; Ascidiidae; Asellidae; Asteriidae; Asterinidae; AWI_Envi; Balanidae; Bangiaceae; Batrachospermaceae; Boldiaceae; Buccinidae; Camaenidae; Capitellidae; Cardiidae; Ceramiaceae; Cercomonadidae; Champiaceae; Chordaceae; Chordariaceae; Cionidae; Clausiliidae; Comatulidae; Conidae; Corallinaceae; Cyanidiaceae; Cypridinidae; Daphniidae; Dasyaceae; Delesseriaceae; Dictyotaceae; Didiniidae; Dixoniellaceae; Dugesiidae; Echinometridae; Ecology & Environment; Ectocarpaceae; Edwardsiidae; Endocladiaceae; Erythrotrichiaceae; Fucaceae; Galaxauraceae; Gelidiaceae; Gigartinaceae; Gracilariaceae; Haliotidae; Halymeniaceae; Harpacticidae; Hildenbrandiaceae; Holostichidae; Hyalellidae; Hyalidae; Hydractiniidae; Kallymeniaceae; KALMAR II; Kronotsky Peninsula; Laminariaceae; Laqueidae; Lessoniaceae; Liagoraceae; Limulidae; Lingulidae; Littorinidae; Lottiidae; Lumbricidae; Lymnaeidae; Lysianassidae; Macrostomidae; Mactridae; Maldanidae; Mastigamoebidae; Megascolecidae; Merulinidae; Molgulidae; Muricidae; Mytilidae; Nephropidae; Nephtheidae; Nereididae; Niphatidae; Oikopleuridae; Ostreidae; Oxystominidae; Palaemonidae; Palmariaceae; Parastacidae; PC; Pectinidae; Penaeidae; Peyssonneliaceae; Philasteridae; Philodinidae; Phyllophoraceae; Piston corer; Pocilloporidae; Polar Terrestrial Environmental Systems @ AWI; Pollicipedidae; Porphyridiaceae; Portunidae; Priapulidae; Protaspidae; Pteriidae; Pterocladiaceae; Pyuridae; Raperosteliaceae; Rhodochaetaceae; Rhodogorgonaceae; Rhodomelaceae; Rhodymeniaceae; Rhytididae; Rossellidae; Sargassaceae; Scalibregmatidae; Schizymeniaceae; Scytosiphonaceae; Sebdeniaceae; Serpulidae; Sertulariidae; Shotgun counts; Siboglinidae; SO201/2; SO201-2-12KL; Solecurtidae; Solieriaceae; Sonne; Spionidae; Stichopodidae; Strongylocentrotidae; Styelidae; Stylonemataceae; Suberitidae; Tellinidae; Tetragonicipitidae; Trichoplacidae; Unionidae; Varunidae; Veneridae; Vesicomyidae; Wrangeliaceae; Zosteraceae
    Type: Dataset
    Format: text/tab-separated-values, 3525 data points
    Location Call Number Limitation Availability
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  • 5
    Publication Date: 2023-07-10
    Keywords: Acanthocerataceae; Acartiidae; Acaryochloridaceae; Acipenseridae; Adinetidae; AGE; Algae & Protists; Amoebophryaceae; Amphipleuraceae; Anarhichadidae; Anaulaceae; Anguillidae; Anomoeoneidaceae; Aphanizomenonaceae; Aphanothecaceae; Apogonidae; Apusomonadidae; Asellidae; Attheyaceae; AWI_Envi; Bacillariaceae; Balaenidae; Balaenopteridae; Bathycoccaceae; Batrachoididae; Biddulphiaceae; Blenniidae; Bovichtidae; Brachionidae; Bracteacoccaceae; Bryopsidaceae; Calanidae; Callorhinchidae; Calotrichaceae; Carangidae; Carcharhinidae; Caulerpaceae; Chaetocerotaceae; Chaetophoraceae; Chamaesiphonaceae; Channichthyidae; Characeae; Chattonellaceae; Chlamydomonadaceae; Chlorellaceae; Chlorobiaceae; Chlorococcaceae; Chlorocystidaceae; Chlorodendraceae; Chloroflexaceae; Chloropicaceae; Chromeraceae; Chromulinaceae; Chroococcaceae; Chroococcidiopsidaceae; Chroomonadaceae; Chrysochromulinaceae; Cirratulidae; Closteriaceae; Clupeidae; Codiaceae; Coelacanthidae; Coleochaetaceae; Coleofasciculaceae; Collodictyonidae; Collophidiidae; Collosphaeridae; Collozoidae; Coscinodiscaceae; Cottidae; Cryptomonadaceae; Cyaneidae; Cyanidiaceae; Cyanophoraceae; Cyanothecaceae; Cyclopettidae; Cyclopteridae; Cymatosiraceae; Delphinidae; Dermocarpellaceae; Desmidiaceae; Diplonemidae; Dunaliellaceae; Ebriacea; Ecology & Environment; Eirenidae; Engraulidae; Entomoneidaceae; Eucalanidae; Euglenaceae; Eunotiaceae; Euphausiidae; Euplotidae; Eustigmataceae; Fonticulaceae; Fragilariaceae; Fundulidae; Gadidae; Gasterosteidae; Geminigeraceae; Ginglymostomatidae; Glaucocystaceae; Globorotaliidae; Gloeobacteraceae; Gloeochaetaceae; Gloeomargaritaceae; Gobiidae; Golenkiniaceae; Gomontiellaceae; Gomphonemataceae; Gonatozygaceae; Gonyaulacaceae; Gymnodiniaceae; Haematococcaceae; Halimedaceae; Hapalosiphonaceae; Heliobacteriaceae; Heliopeltaceae; Hemiaulaceae; Hemidiscaceae; Hemiselmidaceae; Heterocapsaceae; Hexamitidae; Histionidae; Holocentridae; Hydridae; Hydrodictyaceae; Hyellaceae; Isochrysidaceae; Jakobidae; KALMAR II; Kareniaceae; Klebsormidiaceae; Koliellaceae; Kronotsky Peninsula; Kryptoperidiniaceae; Lateolabracidae; Leptocylindraceae; Leptolyngbyaceae; Licmophoraceae; Lipotidae; Lithodesmiaceae; Mallomonadaceae; Mamiellaceae; Merismopediaceae; Mesodiniidae; Mesotaeniaceae; Metopidae; Metridinidae; Microcoleaceae; Microcystaceae; Microsporaceae; Microthamniaceae; Moinidae; Monodontidae; Monodopsidaceae; Monomastigaceae; Mustelidae; Mychonastaceae; Myctophidae; Myxinidae; Naviculaceae; Nephroselmidaceae; Noelaerhabdaceae; Nostocaceae; Octopodidae; Oculatellaceae; Odobenidae; Oedogoniaceae; Oithonidae; Oocystaceae; Oscillatoriaceae; Osmeridae; Ostreobiaceae; Otariidae; Oxytrichidae; Palmellaceae; Palmophyllaceae; Paralichthyidae; Parameciidae; Paulinellidae; Pavlovaceae; PC; Pedinomonadaceae; Pelagiidae; Perkinsidae; Petromyzontidae; Pfiesteriaceae; Phacaceae; Phaeocystaceae; Phaeodactylaceae; Phocidae; Phocoenidae; Physeteridae; Piston corer; Plagiogrammaceae; Pleurastraceae; Pleuronectidae; Pleurosigmataceae; Polar Terrestrial Environmental Systems @ AWI; Polynoidae; Prasinococcaceae; Prasiolaceae; Prochloraceae; Prochlorotrichaceae; Prorocentraceae; Protoperidiniaceae; Prymnesiaceae; Pseudanabaenaceae; Pycnococcaceae; Pyramimonadaceae; Pyrenomonadaceae; Pyrocystaceae; Radiococcaceae; Rajidae; Rhincodontidae; Rhizosoleniaceae; Rivulariaceae; Roseiflexaceae; Rotaliidae; Sagittidae; Salmonidae; Salpingoecidae; Sarcinofilaceae; Scenedesmaceae; Sciaenidae; Scyliorhinidae; Scytonemataceae; Sebastidae; Selenastraceae; Serranidae; Shotgun counts; Siphonocladaceae; Skeletonemataceae; SO201/2; SO201-2-12KL; Sonne; Sparidae; Sphaeropleaceae; Sphaerozoidae; Staurosiraceae; Stephanodiscaceae; Stephanoecidae; Sticholonchidae; Stigonemataceae; Strombidiidae; Suessiaceae; Symbiodiniaceae; Syndiniaceae; Synechococcaceae; Syngnathidae; Temoridae; Terebellidae; Tetrahymenidae; Tetraodontidae; Thalassiosiraceae; Thaumatomastigidae; Thraustochytriaceae; Tolypothrichaceae; Toxariaceae; Trebouxiaceae; Triceratiaceae; Trichiuridae; Triparmaceae; Ulmaridae; Ulnariaceae; Ulotrichaceae; Ulvaceae; Uronemataceae; Vacuolariaceae; Vahlkampfiidae; Volvocaceae; Zygnemataceae
    Type: Dataset
    Format: text/tab-separated-values, 6500 data points
    Location Call Number Limitation Availability
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  • 6
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    PANGAEA
    In:  Supplement to: Harms, Lars; Frickenhaus, Stephan; Schiffer, Melanie; Mark, Felix Christopher; Storch, Daniela; Held, Christoph; Pörtner, Hans-Otto; Lucassen, Magnus (2014): Gene expression profiling in gills of the great spider crab Hyas araneus in response to ocean acidification and warming. BMC Genomics, BMC Genomics, 15(1), 789, https://doi.org/10.1186/1471-2164-15-789
    Publication Date: 2023-09-28
    Description: Hypercapnia and elevated temperatures resulting from climate change may have adverse consequences for many marine organisms. While diverse physiological and ecological effects have been identified, changes in those molecular mechanisms, which shape the physiological phenotype of a species and limit its capacity to compensate, remain poorly understood. Here, we use global gene expression profiling through RNA-Sequencing to study the transcriptional responses to ocean acidification and warming in gills of the boreal spider crab Hyas araneus exposed medium-term (10 weeks) to intermediate (1,120 µatm) and high (1,960 µatm) PCO2 at different temperatures (5°C and 10°C). The analyses reveal shifts in steady state gene expression from control to intermediate and from intermediate to high CO2 exposures. At 5°C acid-base, energy metabolism and stress response related genes were upregulated at intermediate PCO2, whereas high PCO2 induced a relative reduction in expression to levels closer to controls. A similar pattern was found at elevated temperature (10°C). There was a strong coordination between acid-base, metabolic and stress-related processes. Hemolymph parameters at intermediate PCO2 indicate enhanced capacity in acid-base compensation potentially supported by upregulation of a V-ATPase. The likely enhanced energy demand might be met by the upregulation of the electron transport system (ETS), but may lead to increased oxidative stress reflected in upregulated antioxidant defense transcripts. These mechanisms were attenuated by high PCO2, possibly as a result of limited acid-base compensation and metabolic down-regulation. Our findings indicate a PCO2 dependent threshold beyond which compensation by acclimation fails progressively. They also indicate a limited ability of this stenoecious crustacean to compensate for the effects of ocean acidification with and without concomitant warming.
    Keywords: BIOACID; Biological Impacts of Ocean Acidification
    Type: Dataset
    Format: application/vnd.openxmlformats-officedocument.spreadsheetml.sheet, 115.3 kBytes
    Location Call Number Limitation Availability
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  • 7
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    PANGAEA
    In:  Supplement to: Schiffer, Melanie; Harms, Lars; Pörtner, Hans-Otto; Mark, Felix Christopher; Storch, Daniela (2014): Pre-hatching seawater pCO2 affects development and survival of zoea stages of Arctic spider crab Hyas araneus. Marine Ecology Progress Series, 501, 127-139, https://doi.org/10.3354/meps10687
    Publication Date: 2024-03-15
    Description: Sensitivity of marine crustaceans to anthropogenic CO2 emissions and the associated acidification of the oceans may be less than that of other, especially lower, invertebrates. However, effects on critical transition phases or carry-over effects between life stages have not comprehensively been explored. Here we report the impact of elevated seawater PCO2 values (3100 µatm) on Hyas araneus during the last 2 weeks of their embryonic development (pre-hatching phase) and during development while in the consecutive zoea I and zoea II larval stages (post-hatching phase). We measured oxygen consumption, dry weight, developmental time and mortality in zoea I to assess changes in performance. Feeding rates and survival under starvation were investigated at different temperatures to detect differences in thermal sensitivities of zoea I and zoea II larvae depending on pre-hatch history. When embryos were pre-exposed to elevated PCO2 during maternal care, mortality increased about 60% under continued CO2 exposure during the zoea I phase. The larvae that moulted into zoea II, displayed a developmental delay by about 20 days compared to larvae exposed to control PCO2 during embryonic and zoeal phases. Elevated PCO2 caused a reduction in zoea I dry weight and feeding rates, while survival of the starved larvae was not affected by the seawater CO2 concentration. In conclusion, CO2 effects on egg masses under maternal care carried over to the first larval stages of crustaceans and reduced their survival and development to levels below those previously reported in studies exclusively focussing on acute PCO2 effects on the larval stages.
    Keywords: Alkalinity, total; Animalia; Aragonite saturation state; Arctic; Arthropoda; Bicarbonate ion; BIOACID; Biological Impacts of Ocean Acidification; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Coast and continental shelf; Development; Dry mass per individual; Duration, number of days; EXP; Experiment; Feeding rate per individual; Figure; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Heart beat rate; Hyas araneus; Incubation duration; Kongsfjorden_OA; Kongsfjorden, Spitsbergen, Arctic; Laboratory experiment; Larvae; Larvae, dead; Maxilliped beat rate; Mortality/Survival; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; pH, standard deviation; Polar; Potentiometric; Respiration; Respiration rate, oxygen, per individual; Salinity; Salinity, standard deviation; Single species; Species; Stage; Temperature, water; Temperature, water, standard deviation; Zooplankton
    Type: Dataset
    Format: text/tab-separated-values, 16522 data points
    Location Call Number Limitation Availability
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  • 8
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    PANGAEA
    In:  Supplement to: Schiffer, Melanie; Harms, Lars; Pörtner, Hans-Otto; Lucassen, Magnus; Mark, Felix Christopher; Storch, Daniela (2012): Tolerance of Hyas araneus zoea I larvae to elevated seawater PCO2 despite elevated metabolic costs. Marine Biology, 160(8), 1943-1953, https://doi.org/10.1007/s00227-012-2036-0
    Publication Date: 2024-03-15
    Description: Early life stages of marine crustaceans respond sensitively to elevated seawater PCO2. However, the underlying physiological mechanisms have not been studied well. We therefore investigated the effects of elevated seawater PCO2 on oxygen consumption, dry weight, elemental composition, median developmental time (MDT) and mortality in zoea I larvae of the spider crab Hyas araneus (Svalbard 79°N/11°E; collection, May 2009; hatch, December 2009). At the time of moulting, oxygen consumption rate had reached a steady state level under control conditions. In contrast, elevated seawater PCO2 caused the metabolic rate to rise continuously leading to a maximum 1.5-fold increase beyond control level a few days before moulting into the second stage (zoea II), followed by a pronounced decrease. Dry weight of larvae reared under high CO2 conditions was lower than in control larvae at the beginning of the moult cycle, yet this difference had disappeared at the time of moulting. MDT of zoea I varied between 45 ± 1 days under control conditions and 42 ± 2 days under the highest seawater CO2 concentration. The present study indicates that larval development under elevated seawater PCO2 levels results in higher metabolic costs during premoulting events in zoea I. However, H. araneus zoea I larvae seem to be able to compensate for higher metabolic costs as larval MDT and survival was not affected by elevated PCO2 levels.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Animalia; Aragonite saturation state; Arctic; Arthropoda; Bicarbonate ion; BIOACID; Biological Impacts of Ocean Acidification; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbonate ion; Carbonate system computation flag; Carbon content per individual; Carbon dioxide; Coast and continental shelf; Dry mass per individual; EXP; Experiment; Figure; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Hyas araneus; Incubation duration; Kongsfjorden_OA; Kongsfjorden, Spitsbergen, Arctic; Laboratory experiment; Larvae; Larvae, dead; Mortality/Survival; Nitrogen content per individual; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; pH, standard deviation; Polar; Respiration; Respiration rate, oxygen, per individual; Salinity; Single species; Species; Temperature, water; Temperature, water, standard deviation; Zooplankton
    Type: Dataset
    Format: text/tab-separated-values, 26064 data points
    Location Call Number Limitation Availability
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  • 9
    Publication Date: 2024-03-15
    Keywords: Accession number; Acid-base regulation; Alkalinity, total; Alkalinity, total, standard deviation; Animalia; Aragonite saturation state; Arctic; Arthropoda; Benthic animals; Benthos; Bicarbonate ion; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Category; Coast and continental shelf; Comment; Coulometric titration; Description; EXP; Experiment; False discovery rate; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Gene expression, fold change, relative; Gene expression (incl. proteomics); Gene Ontology term; Haemolymph, bicarbonate ion; Haemolymph, partial pressure of carbon dioxide; Haemolymph, pH; Hyas araneus; Laboratory experiment; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, standard deviation; Polar; Potentiometric; Rank; Read length; Salinity; Salinity, standard deviation; Single species; Species; Spitsbergen; Temperature; Temperature, water; Temperature, water, standard deviation; Test set; Treatment
    Type: Dataset
    Format: text/tab-separated-values, 128871 data points
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  • 10
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    PANGAEA
    In:  Supplement to: Iñiguez, Concepcion; Heinrich, Sandra; Harms, Lars; Gordillo, Francisco J L (2017): Increased temperature and CO2 alleviate photoinhibition in Desmarestia anceps: from transcriptomics to carbon utilization. Journal of Experimental Botany, 68(14), 3971-3984, https://doi.org/10.1093/jxb/erx164
    Publication Date: 2024-03-15
    Description: Ocean acidification and warming are affecting polar regions with particular intensity. Rocky shores of the Antarctic Peninsula are dominated by canopy-forming Desmarestiales. This study investigates the physiological and transcriptomic responses of the endemic macroalga Desmarestia anceps to a combination of different levels of temperature (2 and 7 °C), dissolved CO2 (380 and 1000 ppm), and irradiance (65 and 145 µmol photons/m**2/s). Growth and photosynthesis increased at high CO2 conditions, and strongly decreased at 2 °C plus high irradiance, in comparison to the other treatments. Photoinhibition at 2 °C plus high irradiance was evidenced by the photochemical performance and intensive release of dissolved organic carbon. The highest number of differentially regulated transcripts was observed in thalli exposed to 2 °C plus high irradiance. Algal 13C isotopic discrimination values suggested an absence of down-regulation of carbon-concentrating mechanisms at high CO2. CO2 enrichment induced few transcriptomic changes. There was high and constitutive gene expression of many photochemical and inorganic carbon utilization components, which might be related to the strong adaptation of D. anceps to the Antarctic environment. These results suggest that increased temperature and CO2 will allow D. anceps to maintain its productivity while tolerating higher irradiances than at present conditions.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Benthos; Bicarbonate, standard deviation; Bicarbonate ion; Biomass/Abundance/Elemental composition; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calculated using CO2calc; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbon, total; Carbon, total, standard deviation; Carbon/Nitrogen ratio; Carbon/Nitrogen ratio, standard deviation; Carbonate ion; Carbonate ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, standard deviation; Carotenoids; Carotenoids, standard deviation; Chlorophyll a; Chlorophyll a, standard deviation; Chlorophyll c1+c2; Chlorophyll c1+c2, standard deviation; Chromista; Desmarestia anceps; Dissolved organic carbon release rate; Dissolved organic carbon release rate, standard deviation; Experiment duration; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Gross photosynthesis rate, oxygen; Gross photosynthesis rate, standard deviation; Growth/Morphology; Growth rate; Growth rate, standard deviation; Inhibition of net photosynthesis; Inhibition of net photosynthesis, standard deviation; Irradiance; Irradiance, standard deviation; Laboratory experiment; Laboratory strains; Light; Light saturation, standard deviation; Macroalgae; Maximal electron transport rate; Maximal electron transport rate, standard deviation; Maximum photochemical quantum yield of photosystem II; Maximum photochemical quantum yield of photosystem II, standard deviation; Net photosynthesis rate, oxygen; Net photosynthesis rate, standard deviation; Nitrogen, total; Nitrogen, total, standard deviation; Not applicable; OA-ICC; Ocean Acidification International Coordination Centre; Ochrophyta; Other metabolic rates; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Percentage; Percentage, standard deviation; pH; pH, standard deviation; Photosynthetic efficiency; Photosynthetic efficiency, standard deviation; Potentiometric; Potentiometric titration; Primary production/Photosynthesis; Ratio; Ratio, standard deviation; Registration number of species; Respiration; Respiration rate, oxygen; Respiration rate, oxygen, standard deviation; Salinity; Salinity, standard deviation; Saturation light intensity; Single species; Species; Temperature; Temperature, water; Treatment; Type; Uniform resource locator/link to reference; δ13C; δ13C, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 624 data points
    Location Call Number Limitation Availability
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