-
Seawater carbonate chemistry and Hydrozoa, Copepoda abundances and biomasses,...
Anthropogenic CO2 emissions cause a drop in seawater pH and shift the inorganic carbon speciation. Collectively, the term ocean acidification (OA) summarizes these changes. Few... -
Seawater carbonate chemistry and Carbon content, swimming activity (Hz) and m...
Global change is affecting marine ecosystems through a combination of different stressors such as warming, ocean acidification and oxygen depletion. Very little is known about... -
A longitudinal study of Pacific oyster (Crassostrea gigas) larval development...
Three cohorts of Pacific oyster (Crassostrea gigas) larvae at Whiskey Creek Shellfish Hatchery (WCH) in Netarts Bay, Oregon, were monitored for stable isotope incorporation and... -
Effects of pre-hatching pCO2 on development and survival of zoea stages of Ar...
Sensitivity of marine crustaceans to anthropogenic CO2 emissions and the associated acidification of the oceans may be less than that of other, especially lower, invertebrates.... -
Effects of ocean acidification on respiration, growth and C:N ratio of arctic...
Early life stages of marine crustaceans respond sensitively to elevated seawater PCO2. However, the underlying physiological mechanisms have not been studied well. We therefore... -
Carbon content, swimming activity (Hz) and mortality of A. aurita ephyrae und...
This dataset has no description
-
(Table 2) Dry mass, total lipid and wax ester content as well as fatty acid a...
This dataset has no description
-
(Table 3) Dry mass, lipid, carbon and nitrogen content and fatty acid composi...
T. longicornis females were sampled on 12 May 2005 and 5 May 2008 off the island of Helgoland. In 2008, approximately 300 healthy-looking T. longicornis females were incubated... -
Copepod community respiration during POLARSTERN cruise PS81 (ANT-XXIX/1)
This dataset has no description
-
Stable isotope composition of calanoid copepods in the open eastern Atlantic ...
This dataset has no description
-
Dry weight and carbon and nitrogen content of mesozooplankton during Polarste...
Mesozooplankton for experiments was sampled with a 300 µm Bongo net towed vertically over a depth range between depth top and depth bottom at 0.3 m/sec -
Electron transport system (ETS) activity and respiration rates of pelagic dec...
According to Packard (1971) and Owens & King (1975), ETS activities of eight decapod species were measured with an optimised method for pelagic decapods:... -
KOSMOS Bergen 2015 mesocosm study: C. harengus biomass
To evaluate the influence of ocean acidification on predatory plankton, e.g. Hydrozoa and fish larvae as well as their interaction in complex natural communities, we deployed... -
Copepod respiration in the southern Benguela upwelling system during METEOR c...
This dataset has no description
-
Respiration and ingestion rates of calanoid copepod in the northern Benguela ...
Respiration rates of 16 calanoid copepod species from the northern Benguela upwelling system were measured on board RRS Discovery in September/October 2010 to determine their... -
Table 2. Mass, carbon and nitrogen in zoea I of Taliepus dentatus from Chile
This dataset has no description
-
Organic matter and elemental composition of gelatinous and soft-bodied zoopla...
Gelatinous and soft-bodied zooplankton (GZ) have long been considered to have low energetic value and are insufficient to sustain higher trophic levels. However, the nutritional... -
Jellyfish abundance and Chlorophyll a data from a shallow semi-enclosed cove,...
Carnivorous gelatinous zooplankton (GZ) can be very abundant in marine ecosystems around the globe and exert considerable predation pressures on micro- to macrozooplankton as... -
(Supplement Table 1) Individual measurements of prosome length, dry weight an...
We present an accurate, fast, simple and non-destructive photographic method to estimate wax ester and lipid content in single individuals of the calanoid copepod genus Calanus...
