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Negative effects of ocean acidification on calcification vary within the cocc...
A large percentage of CO2 emitted into the atmosphere is absorbed by the oceans, causing chemical changes in surface waters known as ocean acidification (OA). Despite the high... -
Interactive effects of ocean acidification and nitrogen limitation on two blo...
Global climate change involves an increase in oceanic CO2 concentrations as well as thermal stratification of the water column, thereby reducing nutrient supply from deep to... -
The effect of phosphorus limitation and heat stress on calcification in Emili...
Calcifying haptophytes (coccolithophores) sequester carbon in the form of organic and inorganic cellular components (coccoliths). We examined the effect of phosphorus (P)... -
Seawater carbonate chemistry and the incorporation of radio-labeled heavy met...
The marine organisms which inhabit the coastline are exposed to a number of anthropogenic pressures that may interact. For instance, the accumulation of toxic metals present in... -
Seawater carbonate chemistry and growth rate, photosynthetic carbon fixation ...
Marine phytoplankton such as bloom-forming, calcite-producing coccolithophores, are naturally exposed to solar ultraviolet radiation (UVR, 280–400 nm) in the ocean's upper mixed... -
Seawater carbonate chemistry and growth rate, cellular POC, PON, PIC contents
Coccolithophores are important oceanic primary producers not only in terms of photosynthesis but also because they produce calcite plates called coccoliths. Ongoing ocean... -
Seawater carbonate chemistry and calcification of an estuarine coccolithophore
Ocean acidification has the capacity to impact future coccolithophore growth, photosynthesis, and calcification, but experimental culture work with coccolithophores has produced... -
Seawater carbonate chemistry and hatch size and larval growth of walleye poll...
Rising atmospheric concentrations of CO2 are predicted to decrease the pH of high-latitude oceans by 0.3–0.5 units by 2100. Because of their limited capacity for ion exchange,... -
Seawater carbonate chemistry and photoinhibition of the Picophytoplankter Syn...
The marine picocyanobacterium Synechococcus accounts for a major fraction of the primary production across the global oceans. However, knowledge of the responses of... -
Expression of biomineralization-related ion transport genes in Emiliania huxl...
This dataset has no description
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Adaptation of a globally important coccolithophore to ocean warming and acidi...
This dataset has no description
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Long-term dynamics of adaptive evolution in a globally important coccolithoph...
In order to allow full comparability with other ocean acidification data sets, the R package seacarb (Lavigne et al, 2014) was used to compute a complete and consistent set of... -
Responses of the Emiliania huxleyi Proteome to Ocean Acidification
Ocean acidification due to rising atmospheric CO2 is expected to affect the physiology of important calcifying marine organisms, but the nature and magnitude of change is yet to... -
Data set on carbon and nitrogen concentrations, stocks, and isotopic composit...
Data on carbon and nitrogen stocks and stable isotope composition (δ13C, δ15N) in Red Sea seagrass and mangrove sediments The dataset is publically available since May 2019.... -
Seawater carbonate chemistry and Isochrysis sp.'s responses to temperature (2...
We assessed the responses of solitary cells of Arctic Isochrysis sp. grown under a matrix of temperature (2°C vs. 6°C), light intensity (55 vs. 160 μmol photons m-2 s-1) and CO2... -
Belowground soil analysis from the Tibetan Plateau
This dataset has no description
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Bulk parameters during incubation of sediment core 322-C0012
This data set shows the release of dissolved organic matter, hydrogen, hydrogenase, and inorganic ions (manganese, iron, total sulfur, and ammonium) at temperatures of 20°C (in... -
Adult kelp blade carbon and nitrogen content along the depth gradient monitor...
Surveys of C:N ratios, carbon and nitrogen content in the blades of adult kelps at Hansneset, Blomstrand in Kongsfjorden, Svalbard, were performed along a depth transect down to... -
Survival of Mya arenaria and Mya truncata after 12 days in experimental heatw...
Two species of clams, Mya arenaria (1) and Mya truncata (2), were hand collected from Métis-sur-Mer, Québec, Canada (48° 40' 4.6092" N, 68° 1' 5.9484" W) and by SCUBA diving (~... -
Moisture, temperature and light modualte methane oxidation from dry riverbeds...
In this study, under lab conditions (Jan-Apr 2022) in we examined how three key drivers of methane oxidation in soils also modulate methane oxidation (i.e. methanotrophy) in dry...