ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
Collection
Keywords
  • 1
    Publication Date: 2024-01-13
    Description: Internal pH measurements made in the extracellular calcifying medium (ECM), calcifying (calicoblastic) epithelium and mesoglea of the coral Stylophora pistillata using the fluorescent dye SNARF-1 and confocal microscopy. The measurements were made in light and darkness three experiments. Experiment 1 involved using coral samples maintained at pH 8 seawater. Experiment 2 involved placing samples in 4 seawater acidification conditions: pH 8, 7.8, 7.4 and 7.2 for 1 week. Experiment 3 involved placing samples in 4 levels of dissolved inorganic carbon concentration: elevated; ambient, low and very low for one week. The research was carried out at the Centre Scientifique de Monaco between 2014-2017. The aim of the experiment was to determine the pH gradient across the calcifying cell layer and determine how it responded to the three experiments.
    Keywords: biomineralization; Climate change; Comment; Confocal Microscope, Leica, SP5; EXP; Experiment; Experiment/study setup; Laboratory experiment; Laboratory-experiments; pH; pH, extracellular; pH, extracellular, standard deviation; pH, intracellular; pH, intracellular, standard deviation; pH, mesoglea; pH, mesoglea, standard deviation; pH, standard deviation; pH regulation; physiology; Salinity; scleractinians; Species, unique identification; Species, unique identification (Semantic URI); Species, unique identification (URI); Temperature, water; Thermometer; Treatment
    Type: Dataset
    Format: text/tab-separated-values, 201 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Publication Date: 2024-01-13
    Description: Half-time of calcein influx was measured in the coral Stylophora pistillata as a method to investigate paracellular transport. To calculate half-life of calcein influx, time lapses of calcein influx into the extracellular calcifying medium was captured using confocal microscopy. The time lapse data set associated with figure 2 was recorded at 25 degrees in a seawater pH of 8. The study was carried on microcolonies of S. pistillata on glass coverslips. The study was conducted the Centre Scientifque de Monaco between 2016 and 2019.
    Keywords: Calcein; Calcein-influx_experiments; EXP; Experiment; Fluorescence intensity; Parcaellular transport; Time in minutes
    Type: Dataset
    Format: text/tab-separated-values, 46 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Publication Date: 2024-03-15
    Description: Coral calcification relies on the transport of ions and molecules to the extracellular calcifying medium (ECM). Little is known about paracellular transport (via intercellular junctions) in corals and other marine calcifiers. Here, we investigated whether the permeability of the paracellular pathway varied in different environmental conditions in the coral Stylophora pistillata. Using the fluorescent dye calcein, we characterised the dynamics of calcein influx from seawater to the ECM and showed that increases in paracellular permeability (leakiness) induced by hyperosmotic treatment could be detected by changes in calcein influx rates. We then used the calcein-imaging approach to investigate the effects of two environmental stressors on paracellular permeability: seawater acidification and temperature change. Under conditions of seawater acidification (pH 7.2) known to depress pH in the ECM and the calcifying cells of S. pistillata, we observed a decrease in half-times of calcein influx, indicating increased paracellular permeability. By contrast, high temperature (31°C) had no effect, whereas low temperature (20°C) caused decreases in paracellular permeability. Overall, our study establishes an approach to conduct further in vivo investigation of paracellular transport and suggests that changes in paracellular permeability could form an uncharacterised aspect of the physiological response of S. pistillata to seawater acidification.
    Keywords: Acid-base regulation; Alkalinity, total; Animalia; Aragonite saturation state; Benthic animals; Benthos; Bicarbonate ion; Calcification/Dissolution; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Cnidaria; Comment; Containers and aquaria (20-1000 L or 〈 1 m**2); Distance; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Laboratory experiment; Laboratory strains; Not applicable; OA-ICC; Ocean Acidification International Coordination Centre; Other studied parameter or process; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, extracellular; pH, intracellular; Potentiometric titration; Registration number of species; Salinity; Single species; Species; Spectrophotometric; Stylophora pistillata; Temperature, water; Time in minutes; Treatment; Type; Uniform resource locator/link to reference
    Type: Dataset
    Format: text/tab-separated-values, 751 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Publication Date: 2024-03-15
    Description: Ocean warming and ocean acidification (OA) are direct consequences of climate change and affect coral reefs worldwide. While the effect of ocean warming manifests itself in increased frequency and severity of coral bleaching, the effects of ocean acidification on corals are less clear. In particular, long-term effects of OA on the bacterial communities associated with corals are largely unknown. In this study, we investigated the effects of ocean acidification on the resident and active microbiome of long-term aquaria-maintained Stylophora pistillata colonies by assessing 16S rRNA gene diversity on the DNA (resident community) and RNA level (active community). Coral colony fragments of S. pistillata were kept in aquaria for 2 years at four different pCO2 levels ranging from current pH conditions to increased acidification scenarios (i.e., pH 7.2, 7.4, 7.8, and 8). We identified 154 bacterial families encompassing 2,047 taxa (OTUs) in the resident and 89 bacterial families including 1,659 OTUs in the active communities. Resident communities were dominated by members of Alteromonadaceae, Flavobacteriaceae, and Colwelliaceae, while active communities were dominated by families Cyclobacteriacea and Amoebophilaceae. Besides the overall differences between resident and active community composition, significant differences were seen between the control (pH 8) and the two lower pH treatments (7.2 and 7.4) in the active community, but only between pH 8 and 7.2 in the resident community. Our analyses revealed profound differences between the resident and active microbial communities, and we found that OA exerted stronger effects on the active community. Further, our results suggest that rDNA- and rRNA-based sequencing should be considered complementary tools to investigate the effects of environmental change on microbial assemblage structure and activity.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Aragonite saturation state, standard deviation; Benthos; Bicarbonate ion; Bicarbonate ion, standard deviation; 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 ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Chao 1 richness; Chao 1 richness, standard deviation; Chao 1 richness, standard error; Community composition and diversity; Containers and aquaria (20-1000 L or 〈 1 m**2); Entire community; Evenness of species; Evenness of species, standard deviation; Evenness of species, standard error; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Laboratory experiment; Laboratory strains; Not applicable; 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; Rocky-shore community; Salinity; Shannon Diversity Index; Shannon Diversity Index, standard deviation; Shannon Diversity index, standard error; Temperature, water; Treatment; Type
    Type: Dataset
    Format: text/tab-separated-values, 180 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Publication Date: 2024-03-15
    Description: There are increasing concerns that the current rate of climate change might outpace the ability of reef-building corals to adapt to future conditions. Work on model systems has shown that environmentally induced alterations in DNA methylation can lead to phenotypic acclimatization. While DNA methylation has been reported in corals and is thought to associate with phenotypic plasticity, potential mechanisms linked to changes in whole-genome methylation have yet to be elucidated. We show that DNA methylation significantly reduces spurious transcription in the coral Stylophora pistillata. Furthermore, we find that DNA methylation also reduces transcriptional noise by fine-tuning the expression of highly expressed genes. Analysis of DNA methylation patterns of corals subjected to long-term pH stress showed widespread changes in pathways regulating cell cycle and body size. Correspondingly, we found significant increases in cell and polyp sizes that resulted in more porous skeletons, supporting the hypothesis that linear extension rates are maintained under conditions of reduced calcification. These findings suggest an epigenetic component in phenotypic acclimatization that provides corals with an additional mechanism to cope with environmental change.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Animalia; Aragonite saturation state; Aragonite saturation state, standard deviation; Benthic animals; Benthos; Bicarbonate ion; Bicarbonate ion, standard deviation; Calcite saturation state; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Calyx size; Calyx size, standard error; Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbonate ion; Carbonate ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Cell size; Cell size, standard error; Cnidaria; Containers and aquaria (20-1000 L or 〈 1 m**2); Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Laboratory experiment; Laboratory strains; Not applicable; 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; Potentiometric titration; Salinity; Single species; Skeletal porosity; Skeletal porosity, standard error; Species, unique identification; Species, unique identification (Semantic URI); Species, unique identification (URI); Spectrophotometric; Stylophora pistillata; Temperature, water; Treatment; Type of study
    Type: Dataset
    Format: text/tab-separated-values, 68 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Tambutté, Eric; Venn, Alexander A; Holcomb, Michael; Segonds, N; Techer, N; Zoccola, Didier; Allemand, Denis; Tambutté, Sylvie (2015): Morphological plasticity of the coral skeleton under CO2-driven seawater acidification. Nature Communications, 6, 7368, https://doi.org/10.1038/ncomms8368
    Publication Date: 2024-03-19
    Description: Ocean acidification causes corals to calcify at reduced rates, but current understanding of the underlying processes is limited. Here, we conduct a mechanistic study into how seawater acidification alters skeletal growth of the coral Stylophora pistillata. Reductions in colony calcification rates are manifested as increases in skeletal porosity at lower pH, while linear extension of skeletons remains unchanged. Inspection of the microstructure of skeletons and measurements of pH at the site of calcification indicate that dissolution is not responsible for changes in skeletal porosity. Instead, changes occur by enlargement of corallite-calyxes and thinning of associated skeletal elements, constituting a modification in skeleton architecture. We also detect increases in the organic matrix protein content of skeletons formed under lower pH. Overall, our study reveals that seawater acidification not only causes decreases in calcification, but can also cause morphological change of the coral skeleton to a more porous and potentially fragile phenotype.
    Keywords: Acid-base regulation; Alkalinity, total; Alkalinity, total, standard deviation; Animalia; Aragonite saturation state; Aragonite saturation state, standard deviation; Area, standard error; Area in square milimeter; Benthic animals; Benthos; Bicarbonate ion; Bicarbonate ion, standard deviation; Biomass/Abundance/Elemental composition; Calcification/Dissolution; Calcification rate, standard error; Calcification rate of calcium carbonate; Calcifying fluid, pH; Calcifying fluid, pH, standard error; 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 ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Chlorophyll a; Chlorophyll a, per protein; Chlorophyll a, standard error; Chlorophyll a per cell; Chlorophyll c2; Chlorophyll c2, per protein; Chlorophyll c2, standard error; Chlorophyll c2 per cell; Cnidaria; Coast and continental shelf; Corallite, per skeleton surface area; Corallite, per skeleton surface area, standard error; Density, skeletal bulk; Density, skeletal bulk, standard error; Figure; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Laboratory experiment; Linear extension; Linear extension, standard error; Mediterranean Sea; OA-ICC; Ocean Acidification International Coordination Centre; Organic matrix protein, per skeleton; Organic matrix protein, per skeleton, standard error; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, standard deviation; pH, standard error; Photosynthesis rate, oxygen, per protein; Photosynthesis rate of oxygen; Photosynthesis rate of oxygen, per symbiont cell; Photosynthesis rate of oxygen, standard error; Porosity; Porosity, standard error; Potentiometric; Potentiometric titration; Primary production/Photosynthesis; Protein per surface area; Proteins, standard error; Respiration; Respiration rate, oxygen; Respiration rate, oxygen, per protein; Respiration rate, oxygen, standard error; Salinity; Single species; Species; Stylophora pistillata; Symbiont cell density; Symbiont cell density, standard error; Table; Temperature, water; Treatment; Tropical
    Type: Dataset
    Format: text/tab-separated-values, 464 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Holcomb, Michael; Venn, Alexander A; Tambutté, Eric; Tambutté, Sylvie; Allemand, Denis; Trotter, Julie; McCulloch, Malcolm T (2014): Coral calcifying fluid pH dictates response to ocean acidification. Scientific Reports, 4, https://doi.org/10.1038/srep05207
    Publication Date: 2024-03-15
    Description: Ocean acidification driven by rising levels of CO2 impairs calcification, threatening coral reef growth. Predicting how corals respond to CO2 requires a better understanding of how calcification is controlled. Here we show how spatial variations in the pH of the internal calcifying fluid (pHcf) in coral (Stylophora pistillata) colonies correlates with differential sensitivity of calcification to acidification. Coral apexes had the highest pHcf and experienced the smallest changes in pHcf in response to acidification. Lateral growth was associated with lower pHcf and greater changes with acidification. Calcification showed a pattern similar to pHcf, with lateral growth being more strongly affected by acidification than apical. Regulation of pHcf is therefore spatially variable within a coral and critical to determining the sensitivity of calcification to ocean acidification.
    Keywords: Acid-base regulation; Alkalinity, total; Alkalinity, total, standard deviation; Animalia; Aragonite saturation state; Benthic animals; Benthos; Bicarbonate ion; Calcification/Dissolution; Calcifying fluid, pH; Calcifying fluid, pH, standard deviation; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Cnidaria; Coast and continental shelf; Containers and aquaria (20-1000 L or 〈 1 m**2); Difference; Difference, standard deviation; Figure; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Group; Growth, relative; Growth, relative, standard deviation; Growth/Morphology; Identification; Incubation duration; Laboratory experiment; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, standard deviation; Potentiometric; Potentiometric titration; Salinity; Single species; South Pacific; Species; Stylophora pistillata; Temperate; Temperature, water; δ11B; δ11B, standard error
    Type: Dataset
    Format: text/tab-separated-values, 2090 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Comeau, Steeve; Tambutté, Eric; Carpenter, Robert C; Edmunds, Peter J; Evensen, Nicolas R; Allemand, Denis; Ferrier-Pagès, Christine; Tambutté, Sylvie; Venn, Alexander A (2017): Coral calcifying fluid pH is modulated by seawater carbonate chemistry not solely seawater pH. Proceedings of the Royal Society B-Biological Sciences, 284(1847), 20161669, https://doi.org/10.1098/rspb.2016.1669
    Publication Date: 2024-03-15
    Description: Reef coral calcification depends on regulation of pH in the internal calcifying fluid in which the coral skeleton forms. However, little is known about calcifying fluid pH (pHCF) regulation, despite its importance in determining the response of corals to ocean acidification. Here, we investigate the impact of seawater dissolved inorganic carbon (DIC) concentration on calcifying fluid pH in the coral Stylophora pistillata in seawater with manipulated [DIC] and constant pH. Our results reveal that regulation of pHCF and calcification rates are sensitive to changes in seawater [DIC] in the light and dark. While part of this relationship can be explained by changes in rates of photosynthesis and respiration, our data point to the importance of seawater DIC in pH regulation of the coral's calcifying cells. Our findings contribute towards a mechanistic understanding of how and why coral calcification is sensitive to changes in seawater carbonate chemistry, which is needed for predicting effects of environmental change on coral reefs and for robust interpretations of isotopic paleoenvironmental records in coral skeletons.
    Keywords: Acid-base regulation; Alkalinity, total; Alkalinity, total, standard error; Animalia; Aragonite saturation state; Benthic animals; Benthos; Bicarbonate ion; Calcification/Dissolution; Calcification rate, standard error; Calcification rate of calcium carbonate; Calcifying fluid, pH; Calcifying fluid, pH, standard error; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Cnidaria; Containers and aquaria (20-1000 L or 〈 1 m**2); Figure; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Gross photosynthesis rate, oxygen, standard error; Laboratory experiment; Laboratory strains; Net photosynthesis rate, oxygen, standard error; Not applicable; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, standard error; Photosynthesis rate of oxygen, per symbiont cell; Primary production/Photosynthesis; Registration number of species; Respiration; Respiration rate, oxygen; Respiration rate, oxygen, standard error; Salinity; Single species; Species; Stylophora pistillata; Temperature, water; Temperature, water, standard error; Treatment; Type; Uniform resource locator/link to reference
    Type: Dataset
    Format: text/tab-separated-values, 639 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Venn, Alexander A; Tambutté, Eric; Holcomb, Michael; Laurent, Julien; Allemand, Denis; Tambutté, Sylvie (2012): Impact of seawater acidification on pH at the tissue-skeleton interface and calcification in reef corals. Proceedings of the National Academy of Sciences, 110(5), 1634-1639, https://doi.org/10.1073/pnas.1216153110
    Publication Date: 2024-03-15
    Description: Insight into the response of reef corals and other major marine calcifiers to ocean acidification is limited by a lack of knowledge about how seawater pH and carbonate chemistry impact the physiological processes that drive biomineralization. Ocean acidification is proposed to reduce calcification rates in corals by causing declines in internal pH at the calcifying tissue-skeleton interface where biomineralization takes place. Here, we performed an in vivo study on how partial-pressure CO(2)-driven seawater acidification impacts intracellular pH in coral calcifying cells and extracellular pH in the fluid at the tissue-skeleton interface [subcalicoblastic medium (SCM)] in the coral Stylophora pistillata. We also measured calcification in corals grown under the same conditions of seawater acidification by measuring lateral growth of colonies and growth of aragonite crystals under the calcifying tissue. Our findings confirm that seawater acidification decreases pH of the SCM, but this decrease is gradual relative to the surrounding seawater, leading to an increasing pH gradient between the SCM and seawater. Reductions in calcification rate, both at the level of crystals and whole colonies, were only observed in our lowest pH treatment when pH was significantly depressed in the calcifying cells in addition to the SCM. Overall, our findings suggest that reef corals may mitigate the effects of seawater acidification by regulating pH in the SCM, but they also highlight the role of calcifying cell pH homeostasis in determining the response of reef corals to changes in external seawater pH and carbonate chemistry.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Aragonite saturation state, standard deviation; Bicarbonate ion; Bicarbonate ion, standard deviation; Calcification/Dissolution; 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 ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Change; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Group; Identification; Laboratory experiment; Laboratory strains; Location; Micro-nutrients; Not applicable; 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; Potentiometric titration; Replicate; Salinity; Species; Stylophora pistillata; Surface area; Temperature, water; Treatment
    Type: Dataset
    Format: text/tab-separated-values, 2880 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Laurent, Julien; Venn, Alexander A; Tambutté, Eric; Ganot, Philippe; Allemand, Denis; Tambutté, Sylvie (2014): Regulation of intracellular pH in cnidarians: response to acidosis in Anemonia viridis. FEBS Journal, 281(3), 683-695, https://doi.org/10.1111/febs.12614
    Publication Date: 2024-03-15
    Description: The regulation of intracellular pH (pHi) is a fundamental aspect of cell physiology that has received little attention in studies of the phylum Cnidaria, which includes ecologically important sea anemones and reef-building corals. Like all organisms, cnidarians must maintain pH homeostasis to counterbalance reductions in pHi, which can arise because of changes in either intrinsic or extrinsic parameters. Corals and sea anemones face natural daily changes in internal fluids, where the extracellular pH can range from 8.9 during the day to 7.4 at night. Furthermore, cnidarians are likely to experience future CO2-driven declines in seawater pH, a process known as ocean acidification. Here, we carried out the first mechanistic investigation to determine how cnidarian pHi regulation responds to decreases in extracellular and intracellular pH. Using the anemone Anemonia viridis, we employed confocal live cell imaging and a pH-sensitive dye to track the dynamics of pHi after intracellular acidosis induced by acute exposure to decreases in seawater pH and NH4Cl prepulses. The investigation was conducted on cells that contained intracellular symbiotic algae (Symbiodinium sp.) and on symbiont-free endoderm cells. Experiments using inhibitors and Na-free seawater indicate a potential role of Na/H plasma membrane exchangers (NHEs) in mediating pHi recovery following intracellular acidosis in both cell types. We also measured the buffering capacity of cells, and obtained values between 20.8 and 43.8 mM per pH unit, which are comparable to those in other invertebrates. Our findings provide the first steps towards a better understanding of acid-base regulation in these basal metazoans, for which information on cell physiology is extremely limited.
    Keywords: Acid-base regulation; Alkalinity, total; Alkalinity, total, standard deviation; Anemonia viridis; Animalia; Aragonite saturation state; Benthic animals; Benthos; Bicarbonate ion; Bicarbonate ion, standard deviation; 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 ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Cnidaria; Coast and continental shelf; Figure; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Laboratory experiment; Mediterranean Sea; 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, intracellular; pH, intracellular, standard error; pH, standard deviation; Potentiometric; Potentiometric titration; Respiration; Respiration rate, oxygen, per protein; Respiration rate, oxygen, standard error; Salinity; Single species; Species; Spectrophotometric; Temperate; Temperature, water; Time in minutes; Treatment
    Type: Dataset
    Format: text/tab-separated-values, 1999 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...