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Elemental composition and residual water content of seven thaliacean (salps a...
Ecosystem models often use wet weights to parameterise biota disregarding their water content. This may be especially erroneous for gelatinous plankton, such as salps and... -
Seawater carbonate chemistry and standard metabolic rate, clearance rate, sur...
In this study, juvenile northern bay scallops Argopecten irradians (Lamarck) that had been reared since 4 h post-fertilization under one of 2 OA conditions (~500–600 or ~750–850... -
Seawater carbonate chemistry and live coral performance vs. framework dissolu...
Physiological sensitivity of cold-water corals to ocean change is far less understood than of tropical corals and very little is known about the impacts of ocean acidification... -
Seawater carbonate chemistry and performance and oxidative status in a tolera...
Whereas low levels of thermal stress, irradiance, and dietary restriction can have beneficial effects for many taxa, stress acclimation remains understudied in marine... -
Seawater carbonate chemistry and net community calcification (NCC) and net co...
There is a long history of examining the impacts of nutrient pollution and pH on coral reefs. However, little is known about how these two stressors interact and influence coral... -
Seawater carbonate chemistry and tissue biomass composition, calcification of...
Ocean acidification (OA) is predicted to reduce reef coral calcification rates and threaten the long-term growth of coral reefs under climate change. Reduced coral growth at... -
Acidification alters predator-prey interactions of blue crab Callinectes sapi...
Acidification due to anthropogenic CO2 pollution, along with episodic or persistent acidification that occurs in coastal environments, will likely result in severe seasonal... -
Biogeographic variability in the physiological response of the cold-water cor...
While ocean acidification is a global issue, the severity of ecosystem effects is likely to vary considerably at regional scales. The lack of understanding of how... -
Long-term effects of altered pH and temperature on the feeding energetics of ...
This study investigated the effects of long-term incubation to near-future combined warming (+2 °C) and ocean acidification (-0.3 and -0.5 pH units) stressors, relative to... -
Effects of reduced and business-as-usual CO2 emission scenarios on the algal ...
Turf algae are a very important component of coral reefs, featuring high growth and turnover rates, whilst covering large areas of substrate. As food for many organisms, turf... -
Sea urchins in a high CO2 world: partitioned effects of body-size, ocean warm...
Body-size and temperature are the major factors explaining metabolic rate, and the additional factor of pH is a major driver at the biochemical level. These three factors have... -
Adult acclimation to combined temperature and pH stressors significantly enha...
This study examined the effects of long-term culture under altered conditions on the Antarctic sea urchin, Sterechinus neumayeri. Sterechinus neumayeri was cultured under the... -
One size fits all: stability of metabolic scaling under warming and ocean aci...
Responses by marine species to ocean acidification (OA) have recently been shown to be modulated by external factors including temperature, food supply and salinity. However the... -
Size matters: plasticity in metabolic scaling shows body-size may modulate re...
Variability in metabolic scaling in animals, the relationship between metabolic rate ( R) and body mass ( M), has been a source of debate and controversy for decades. R is... -
Tolerance of juvenile barnacles (Amphibalanus improvisus) to warming and elev...
We investigated the impacts of warming and elevated pCO2 on newly settled Amphibalanus improvisus from Kiel Fjord, an estuarine ecosystem characterized by significant natural... -
Biogeochemical and phospholipid-derived fatty acid (PLFA) composition of shal...
During R/V Sonne cruise SO254, we conducted ex-situ experiments with shallow- and deep-water demo- and hexactinellid sponges from New Zealand. Over a period of 5 hours, the... -
Tissue carbon, nitrogen and phosphorus composition of Euphausia superba and S...
Samples were collected between 03/26/2018 and 04/27/2018 around the northern tip of the Antarctic Peninsula (63° 0' 1.843'' S, 60° 0' 16.901''W) onboard the RV Polarstern during... -
Gut carbon, nitrogen and phosphorus composition of Euphausia superba and Salp...
Samples were collected between 03/26/2018 and 04/27/2018 around the northern tip of the Antarctic Peninsula (63° 0' 1.843'' S, 60° 0' 16.901''W) onboard the RV Polarstern during... -
Biogeochemical and phospholipid-derived fatty acid (PLFA) composition of deep...
During R/V Sonne cruise SO254 around New Zealand (January-February 2017), deep-sea sponges were incubated in-situ and ex-situ to measure oxygen consumption, inorganic nutrient... -
Wet, dry and ash free dry mass in relation to length of the Mytilidae Aulacom...
Total wet mass (WM), dry mass (DM) and ash free dry mass (AFDM) were determined for specimens from Station 1 (X-Huinay) covering the entire size range of Aulacomya atra and...