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Impact of ocean acidification on thermal tolerance and acid-base regulation o...
In order to allow full comparability with other ocean acidification data sets, the R package seacarb (Gattuso et al, 2015) was used to compute a complete and consistent set of... -
Impact of elevated pCO2 on acid-base regulation of the sea urchin Echinometra...
Due to their low metabolism and apparent poor ion regulation ability, sea urchins could be particularly sensitive to ocean acidification resulting from increased dissolution of... -
The O2, pH and Ca2+ Microenvironment of Benthic Foraminifera in a High CO2 Wo...
Ocean acidification (OA) can have adverse effects on marine calcifiers. Yet, phototrophic marine calcifiers elevate their external oxygen and pH microenvironment in daylight,... -
Effects of Ocean Acidification and Warming on Sperm Activity and Early Life S...
Larval stages are among those most vulnerable to ocean acidification (OA). Projected atmospheric CO2 levels for the end of this century may lead to negative impacts on... -
Effects of drought on generation 2 Lupinus nipomensis (Fabaceae)
Data are for Lupinus nipomensis grown in a dry-down drought experiment at UC Santa Barbara in a second (F1) generation to test for maternal effects on plant growth and... -
Effects of drought on generation 1 Lupinus nipomensis (Fabaceae)
Data are for Lupinus nipomensis grown in a dry-down drought experiment at UC Santa Barbara. Plants were grown in dry-down and well-watered conditions in order to simulate... -
Effects of drought on generation 2 Lupinus bicolor (Fabaceae)
Data are for Lupinus bicolor grown in a dry-down drought experiment at UC Santa Barbara in a second (F1) generation to test for maternal effects on plant growth and reproductive... -
Effects of drought on generation 1 Lupinus bicolor (Fabaceae)
Data are for Lupinus bicolor grown in a dry-down drought experiment at UC Santa Barbara. Plants were grown in dry-down and well-watered conditions in order to study potential... -
Effects of sediment load on buoyant mass and calcification of the juvenile co...
The table shows the mass of the horizontal and vertical downwards oriented corals over the experimental period, measured at the beginning (week 0), in the middle (week 6) and at... -
Effects of sediment load on calyx diameter of the juvenile cold-water coral C...
The table shows the calyx diameters of the corals measured in ImageJ (Version 1.53), separated according to exposed sediment concentration at the beginning of the experiment... -
Ash-Free-Dry-Mass and oxygen consumption of the juvenile cold-water coral Car...
Table shows the dry mass (dm) and ash-free dry mass (AFDM) of Caryophyllia huinayensis individuals used for the respiration experiment. Furthermore, the sediment concentration... -
Egg production rates of Temora longicornis under different nutrient regimes
This dataset has no description
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Macrozoobenthos abundance on a tropical oyster culture in an Amazon estuary, ...
The present study describes the biofouling composition of the surface of the mangrove oyster Crassostrea rhizophorae (Guilding, 1828), cultivated in an Amazon estuary, located... -
Body temperature and immune performance along the life cycle of the tegu liza...
Multiple factors can influence the immune response of vertebrate ectotherms, including body temperature, gonadal steroids, and seasonality, in ways that are thought to reflect... -
Oxygen consumption (resting and after treatment), immune variables and hormon...
To understand the possible interactions between steroid hormones (androgens [AN] and corticosterone [CORT]), metabolism, and immunity during fluctuations of environmental... -
Baseline and after stressor salivary corticosterone levels in the saliva and ...
Glucocorticoids have been widely used as a physiological marker of stress, and elevated baseline glucocorticoids levels in vertebrates have been associated with environmental... -
Plant-pollinator interactions along an elevational gradient on Mt. Kilimanjaro
This data set contains 67 quantitative plant-pollinator networks consisting of 268 observational hours and 4380 plant-pollinator interactions, which were recorded along a 3.4 km... -
Ratio of p-eIF2α vs. eIF2α of anurans from a Brazilian semi-arid area, Caatinga
This dataset has no description
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Phosphorylated eukaryotic initiation factor 2α (p-eIF2α) of anurans from a Br...
This dataset has no description
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Chaperone proteins HSP90 of anurans from a Brazilian semi-arid area, Caatinga
This dataset has no description