Schade, Hanna; Mevenkamp, Lisa; Guilini, Katja; Meyer, Stefanie; Gorb, Stanislav N; Abele, Doris; Vanreusel, Ann; Melzner, Frank (2016): Experiment on effects of elevated pCO2 on bivalve dominated communities. PANGAEA, https://doi.org/10.1594/PANGAEA.870724, Supplement to: Schade, H et al. (2016): Simulated leakage of high pCO2 water negatively impacts bivalve dominated infaunal communities from the Western Baltic Sea. Scientific Reports, 6, 31447, https://doi.org/10.1038/srep31447
Always quote citation above when using data! You can download the citation in several formats below.
Sandy communities were exposed to six different seawater pCO2 regimes for a total of three months (17.12.2011–06.03.2012) in a climate - controlled room. Six header tanks were continuously supplied with filtered seawater from Kiel Fjord, each one connected to six experimental units (EU) ensuring continuous seawater supply. Each EU consisted of a round plastic container with a volume of 12.5 L containing ca. 9.5 L of sediment and an overlying water column of ca. 3 L. The lower 10 cm of the sediment consisted of sieved sand taken from a local beach (Kiel, Falckenstein: 54°23,66 N; 10°11.56 E) while the upper 10 cm consisted of surface sediment from the station at which the experimental animals were sampled to resemble natural conditions as well as to provide naturally occurring microbial and meiofauna communities. Bivalves and sediment were sampled in Kiel Fjord at Falckenstein with a Van Veen grab in 1–2 m depth and kept in holding basins at 9 °C before being placed in EUs.
Numbers per EU simulated a natural size distribution: 5 M. arenaria (size classes: 0.5–1 cm: 2 animals; 1–1.5 cm: 2 animals; 2–2.5 cm: 1 animal), 1 M. balthica, and 40 C. edule (size classes: 0–0.5 cm: 3 animals; 0.5–1 cm: 18 animals; 1–1.5 cm: 11 animals; 1.5–2 cm: 7 animals; 2–2.5 cm: 1 animal). Small gastropods (exclusively Hydrobia spp.) were abundant with ~10 individuals per EU. Due to their small size (< 0.5 mm) they were randomly distributed within all EUs with the sieved sediment. Due to the natural low diversity of the Baltic, the density of other macrofauna individuals was < 1 individuals per m². These low abundant species (e.g. nereid polychaetes, pharid bivalve species) were excluded from the experiment. The EUs were kept in a seawater flow-through system for two weeks under control conditions prior to the experiment to allow proper acclimatization of biogeochemistry and the faunal community. Seawater pH was maintained in the header tanks using a pH feedback system (IKS Aquastar, iksComput- ersysteme GmbH, Karlsbad, Germany). Treatment levels were achieved through continuous addition of acidified water from the header tanks into the overlaying seawater of each EU and included levels of 900 µatm (control, pH 7.8 NBS scale), 1,500 µatm (pH 7.7), 2,900 µatm (pH 7.4), 6,600 µatm (pH 7.0), 12,800 µatm (pH 6.7), and 24,400 µatm (pH 6.4). 900 µatm was used as a control due to the high background pCO2 in Kiel Fjord. To support the bivalve nutritional needs unicellular algae (Rhodomonas sp.) were cultured and added continuously into the header tanks via a peristaltic pump, thus maintaining a stable concentration of 3,500–4,000 cells ml−1 within header tanks. A flow rate of 100 ml min−1 was provided to each EU from the respective header tank via gravity feed.
Throughout the experiment, pH, salinity, temperature, and flow rate were measured daily in each replicate. Salinity and temperature fluctuated in accordance with naturally occurring changes in Kiel Fjord seawater (14.6–20.5 psu and 4.3–8.9 °C, respectively). Light conditions were similar for all EUs. Dead animals were removed daily and behaviour of bivalves (presence/absence on the sediment surface) was noted every other day starting in the third experimental week. Carbonate chemistry and algae concentration in the EUs were measured weekly. Dissolved inorganic carbon (CT) was measured using an Automated Infrared Inorganic Carbon Analyzer (AIRICA, Marianda, Kiel, Germany). Seawater chemistry (pCO2 and calcium carbonate saturation state) was then calculated according to the guide to best practices for ocean CO2 measurements, using CO2SYS57 with pH (NBS scale) and CT, temperature, salinity, and first and second dissociation constants of carbonic acid in seawater.
Date/Time Start: 2011-12-07T00:00:00 * Date/Time End: 2012-03-08T00:00:00
Datasets listed in this publication series
- Schade, H (2016): Experiment on effects of elevated pCO2 on bivalve dominated communities: Bacterial counts. https://doi.org/10.1594/PANGAEA.843729
- Schade, H (2016): Experiment on effects of elevated pCO2 on bivalve dominated communities: Carbon chemistry. https://doi.org/10.1594/PANGAEA.870993
- Schade, H (2016): Experiment on effects of elevated pCO2 on bivalve dominated communities: Cerastoderma edule size and mass. https://doi.org/10.1594/PANGAEA.870723
- Schade, H (2016): Experiment on effects of elevated pCO2 on bivalve dominated communities: Experimental conditions. https://doi.org/10.1594/PANGAEA.870735
- Schade, H (2016): Experiment on effects of elevated pCO2 on bivalve dominated communities: Meiofauna counts and nematode identification. https://doi.org/10.1594/PANGAEA.870688
- Schade, H (2016): Experiment on effects of elevated pCO2 on bivalve dominated communities: Mortality. https://doi.org/10.1594/PANGAEA.870751
- Schade, H (2016): Experiment on effects of elevated pCO2 on bivalve dominated communities: Tissue concentration of malondialdehyde. https://doi.org/10.1594/PANGAEA.870831