140 datasets found

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...

Sea-ice diatoms are known to accumulate in large aggregates in and under the sea ice including melt ponds. In the Arctic, they can contribute substantially to particle export...

In order to allow full comparability with other ocean acidification data sets, the R package seacarb (Lavigne and Gattuso, 2011) was used to compute a complete and consistent...

This is a historical dataset that was published in 1939 by Ad. Steuer and concerns of the faunistic report on the Sipunculoidea, Phoronidea, Brachiopoda, Enteropneusta and...

This is a historical dataset that was published in 1936 by H. Helfer and concerns of the faunistic report on the Pantopoda collected during the floristical and faunistical...

This is a historical dataset that was published in 1936 by Schellenberg A. and concerns of the faunistic report on the Amphipoda collected during the floristical and faunistical...

Abundance and biomass of <i>Tachidius discipes</i> life stages sampled every 3 days between 21 March and 25 June 1979 in the 'Dievengat' (Knokke). The data were...

Data were collected in the framework of a thesis study. The general aim was to give a detailed inventory of the nematode communities present in the Westerschelde area, based on...

Study on meiobenthos and nematode communities (counts, density, biomass, genus composition) collected in the Arctic Ocean in August and September 1991. The data were digitized...

This is a historical dataset that was published in 1938 by A. Steuer and concerns of the faunistic report on the Cumacea, Stomatopoda and Leptostracacollected during the...

Eurasian Jays Garrulus glandarius (Corvidae, n = 16) were trapped in Caldern, Hesse, Central Germany in the years 2020 and 2021 to check for the presence of haemosporidian...

Water parameters in the 2 years before spawning of F0 (08.02.2016-06.03.2018) and during larval and juvenile phase of F1: Larval period until 17.05.2018 (48 dph, 900 dd) and...

Increasing CO2 levels in the surface water of oceans are expected to decrease oceanic pH and lead to seawater acidification. The responses of macroalgaea to this acidification...

Changes in marine environments, including pH changes, have been correlated to alterations in the physiology and disease susceptibility of cultured organisms at the early stages...

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...

Understanding how copepods may respond to ocean acidification (OA) is critical for risk assessments of ocean ecology and biogeochemistry. The perception that copepods are...

We investigated the effects of elevated pCO2 in seawater both on the acute mortality and the reproductive properties of the benthic copepod Tigriopus japonicus and gastropod...

Stream benthic macroinvertebrates were collected for a period of 3 consecutive months (December 2019 to March 2020), in 4 nested/non-nested sites within the catchment of Val...

Abundance and biomass of <i>Tachidius discipes</i> life stages sampled every 3 days between 21 March and 25 June 1979 in the 'Dievengat' (Knokke). The data were...

Data were collected in the framework of a thesis study. The general aim was to give a detailed inventory of the nematode communities present in the Westerschelde area, based on...