Dataset - B2FIND

Additional bottle chemistry values (ta, tco2, stable water isotopes, nutrient...

These data comprise previously published and additional CTD rosette bottle data including PO₄, Si(OH)₄, NH₃, NO₂, NO₃, δ¹⁸O, δ²H, TA and tCO₂ measurements obtained during the...

Additional bottle chemistry values (ta, tco2, stable water isotopes, nutrient...

These data comprise previously published and additional CTD rosette bottle data including PO₄, Si(OH)₄, NH₃, NO₂, NO₃, δ¹⁸O, δ²H, TA and tCO₂ measurements obtained during the...

Seawater carbonate chemistry and behavior of European sea bass (Dicentrarchus...

In order to allow full comparability with other ocean acidification data sets, the R package seacarb (Gattuso et al, 2016) was used to compute a complete and consistent set of...

Seawater carbonate chemistry and the behaviour and growth of a range extendin...

We used a controlled laboratory experiment to test the concurrent effects of projected future summer and winter ocean temperatures, ocean acidification, and novel species...

Seawater carbonate chemistry and bioaccumulation of inorganic and organic mer...

The bioaccumulation of mercury (Hg) in marine organisms through various pathways has not yet been fully explored, particularly in cephalopods. This study utilises radiotracer...

Seawater carbonate chemistry and reproduction in a marine invertebrate

Climate change research is advancing to more complex and more comprehensive studies that include long-term experiments, multiple life-history stages, multi-population, and...

Seawater carbonate chemistry and swimming performance of Tritia reticulata (L...

Tritia reticulata (L.) is a neogastropod ubiquitous in the coastal communities of the NE Atlantic. Its life cycle relies on the swimming performance of planktonic early life...

Seawater carbonate chemistry and mortality, morphology, feeding rate, metabol...

Ocean warming (OW) and acidification (OA) are key features of global change and are predicted to have negative consequences for marine species and ecosystems. At a smaller scale...

Seawater carbonate chemistry and 109Cd, 57Co, and 134Cs bioconcentration by t...

The uptake and depuration kinetics of dissolved 109Cd, 57Co and 134Cs were determined experimentally in the European flat oyster Ostrea edulis (Linnaeus, 1758) under different...

Limited effects of increased CO2 and temperature on metal and radionuclide bi...

This study investigated the combined effects of reduced pH and increased temperature on the capacities of the Pacific cupped oyster Crassostrea gigas to bioconcentrate...

Foraging behaviour of the epaulette shark Hemiscyllium ocellatum is not affec...

Increased oceanic uptake of atmospheric carbon dioxide (CO2) is a threat to marine organisms and ecosystems. Among the most dramatic consequences predicted to date are...

Elevated CO2 affects the behavior of an ecologically and economically importa...

We tested the effect of near-future CO2 levels (= 490, 570, 700, and 960 µatm CO2) on the olfactory responses and activity levels of juvenile coral trout, Plectropomus...

(Table 1, page 119) 10Be and 9Be concentrations in manganese nodules of the P...

The usefulness of cosmogenic beryllium-10 (half life = 2.5 Ma) for studying the rates of accumulation of ferromanganese nodules is reported based on its measured depth...

Valve gape activity of cultured Gigantidas childresse: mean data

Valve gape activity of cultured G. childressi mussels from different nutritional treatments (CH4: 'M', algae + CH4: 'MA', algae: 'A') at changing seawater CH4 concentrations....

Valve gape activity of cultured Gigantidas childresse: individual data

Valve gape activity of cultured G. childressi mussels from different nutritional treatments (CH4: 'M', algae + CH4: 'MA', algae: 'A') in response to mean steps (including both,...