Combined impacts of elevated CO2 and anthropogenic noise on European sea bass (Dicentrarchus labrax)

Ocean acidification (OA) and anthropogenic noise are both known to cause stress and induce physiological and behavioural changes in fish, with consequences for fitness. OA is also predicted to reduce the ocean's capacity to absorb low-frequency sounds produced by human activity. Consequently, anthropogenic noise could propagate further under an increasingly acidic ocean. For the first time, this study investigated the independent and combined impacts of elevated carbon dioxide (CO2) and anthropogenic noise on the behaviour of a marine fish, the European sea bass (Dicentrarchus labrax). In a fully factorial experiment crossing two CO2 levels (current day and elevated) with two noise conditions (ambient and pile driving), D. labrax were exposed to four CO2/noise treatment combinations: 400 µatm/ambient, 1000 µatm/ambient, 400 µatm/pile-driving, and 1000 µatm/pile driving. Pile-driving noise increased ventilation rate (indicating stress) compared with ambient noise conditions. Elevated CO2 did not alter the ventilation rate response to noise. Furthermore, there was no interaction effect between elevated CO2 and pile-driving noise, suggesting that OA is unlikely to influence startle or ventilatory responses of fish to anthropogenic noise. However, effective management of anthropogenic noise could reduce fish stress, which may improve resilience to future stressors.

Abundance of calcareous nannofossils in sediments of the Fram Strait

Sediment cores from the Fram Strait are dated by means of calcareous nannofossil biostratigraphy and are shown to represent, at the most, the last 300 kyr (oxygen isotope stages 1-8). Differences in sedimentation rates are mainly controlled by the bottom topography and the intensity of ice-rafted deposition. Sedimentation rates are normally in the order of a few centimeters per kiloyear in the central Fram Strait but increase to over 10 cm/kyr in cores located on the continental slope. The highest sediment accumulation rates occurred on the shelf (several tens of centimeters per kiloyear).

Grain size and description on gravity core samples from ANT-IV/2 expedition to the Bransfield Strait

From the above and the grafical results it can be concluded that cores in the research area are locally dominated by turbiditic sequences, which can be observed by a strong increase in coarser sediment (>35 µm). These coarser intercalations are lacking in the vicinity of basaltic seamounts, probably due to a shadowing effect of the seamounts. The infill of the King George Basin might be dominated by a north eastern current. Sedimentary structures as observed in the cores are often lacking or vague due to hydrothermal effects (Suess, L, 1986).

Fluor and opal in surface sediment from the Bransfield Strait (Table 1)

The influence of biogenic opal sediment input (mainly diatom skeletons) on the fluorine budget of marine sediments will be shown for 24 sampling stations of the antarctic regions of Bransfield Strait, Powell Basin, South Orkney Plateau and northwestern Weddell Sea. 4 bulk samples, one from each sedimentation area, contain 9 to 28 wt.-% of biogenic opal , the clay fraction of the 24 samples investigated have 2 to 82 wt.-%. The fluorine concentration in the amorphous biogenic component is 15 ppm. 300 to 800 ppm of fluorine were measured in the clay fractions, 330 to 920 ppm in their lithogenic components. Biogenic opal causes a decrease in fluorine concentration of the sediment by a considerable amount: 6 to 56 % relative to the clay fraction, due to the proportions involved. Biogenic opal is therefore taken into account as a 'diluting' factor for the fluorine budget in marine sediments.

AWI Bathymetric Chart of the Fram Strait (BCFS) (Scale 1:100,000)

Based on data from R/V Polarstern multibeam sonar surveys between 1984 and 1997 a high resolution bathymetry has been generated for the central Fram Strait. The area ensonified covers approx. 36,500 sqkm between 78°N - 80°N and 0°E - 7.5°E. Basic outcome of the investigation is a Digital Terrain Model (DTM) with 100 m grid spacing which was utilized for contouring and generation of a new series of bathymetric charts at a scale of 1:100,000, the AWI Bathymetric Chart of the Fram Strait (AWI BCFS).

(Table 1) Main constituents of coccolith size fractions expressed as carbonate contribution at Bass River during the PETM

Coccoliths, calcite plates produced by the marine phytoplankton coccolithophores, have previously shown a large array of carbon and oxygen stable isotope fractionations (termed "vital effects"), correlated to cell size and hypothesized to reflect the varying importance of active carbon acquisition strategies. Culture studies show a reduced range of vital effects between large and small coccolithophores under high CO2, consistent with previous observations of a smaller range of interspecific vital effects in Paleocene coccoliths. We present new fossil data examining coccolithophore vital effects over three key Cenozoic intervals reflecting changing climate and atmospheric partial pressure of CO2 (pCO2). Oxygen and carbon stable isotopes of size-separated coccolith fractions dominated by different species from well preserved Paleocene-Eocene thermal maximum (PETM, ~56 Ma) samples show reduced interspecific differences within the greenhouse boundary conditions of the PETM. Conversely, isotope data from the Plio-Pleistocene transition (PPT; 3.5-2 Ma) and the last glacial maximum (LGM; ~22 ka) show persistent vital effects of ~2 per mil. PPT and LGM data show a clear positive trend between coccolith (cell) size and isotopic enrichment in coccolith carbonate, as seen in laboratory cultures. On geological timescales, the degree of expression of vital effects in coccoliths appears to be insensitive topCO2 changes over the range ~350 ppm (Pliocene) to ~180 ppm (LGM). The modern array of coccolith vital effects arose after the PETM but before the late Pliocene and may reflect the operation of more diverse carbon acquisition strategies in coccolithophores in response to decreasing Cenozoic pCO2.