Radiocarbon ages of sediment core PG1414-2 from Beall Lake, Windmill Islands

A mid-Holocene climate optimum is inferred from a palaeosalinity reconstruction of a closed saline lake (Beall Lake) from the Windmill Islands, East Antarctica using an expanded diatom salinity weighted averaging (WA) regression and calibration model. The addition of 14 lakes and ponds from the Windmill Islands, East Antarctica, to an existing weighted averaging regression and calibration palaeosalinity model of 33 lakes from the Vestfold Hills, East Antarctica expands the number of taxa and lakes and the range of salinity in the existing model and improves the model's predictive ability. This improved model was used to infer Holocene changes in lake water salinity in Beall Lake, Windmill Islands. Six changes in diatom-inferred salinity in Beall Lake are put into broad chronological context based on three radiocarbon dates: as the East Antarctic Ice Sheet (EAIS) retreated from the Windmill Islands during the early Holocene (~9000-8130 corr. yr BP), Beall Lake formed as a melt water-fed freshwater lake, which gradually became more saline as marine influence increased from ~8000 corr. yr BP. Between ~8000 and 4800 corr. yr BP, the diatom assemblage included planktonic marine taxa such as Chaetoceros spp. and cryophilic taxa such as Fragilariopsis cylindrus, which indicate favourable summer growth conditions. A mid-Holocene warm period produced a climate that was warmer and more humid with increased precipitation and snow accumulation. This is reflected in the Beall Lake core as a reduction in the salinity of the lake diatom assemblage from ~4800-4600 corr. yr BP. Holocene isostatic uplift rates in the Windmill Islands vary from 5-6 m/1000 yr. By applying this uplift rate, it is calculated that the bedrock would have risen above sea level by ~4000 yr BP. The Beall Lake core diatom assemblage from ~4600-2900 corr. yr BP includes both marine cryophilic and planktonic taxa together with freshwater benthic and planktonic lacustrine taxa. This mix of species indicates the emergence of the lake from the sea around ~4600 corr. yr BP. From ~2800 corr. yr BP, retreat of the ice margin led to increasing melt water inputs and associated freshening of the lake basin until ~1900 corr. yr BP. The lake basin had no oceanic influence by this time, allowing a terrestrial freshwater flora to establish and thrive for the next ~1000 yr. At ~1850 corr. yr BP, a sudden and rapid salinity change is evident in Beall Lake. A late Holocene warm period between 2000 and 1000 yr BP has been observed in ice core records from Law Dome (an ice cap abutting the Windmill Islands to the east and north). It is therefore inferred that, at ~1850 corr. yr BP, summer temperatures within the Beall Lake catchment area were much higher than present summer temperatures. The climate optimum identified in the Beall Lake core ~4800 yr BP confirms mid-Holocene warming of the Windmill Islands and suggests a synchronous mid-Holocene climate optimum occurred across coastal East Antarctica. In addition, the abrupt climate change inferred at ~1850 yr BP suggests that higher resolution sampling of sediment cores from coastal East Antarctic limnological oases will provide more evidence of rapid climate change events over coastal East Antarctica in future.

Respiration and ingestion rates of calanoid copepod in the northern Benguela Current System measured ex situ during the RSS Discovery D356 cruise in 2010

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 energy requirements and assess their significance in the carbon cycle. Copepod species were sampled by different net types. Immediately after the hauls, samples were sorted to species and stages (16 species; females, males and C5 copepodids) according to Bradford-Grieve et al. (1999). Specimens were kept in temperature-controlled refrigerators for at least 12 h before they were used in experiments. Respiration rates of different copepod species were measured onboard by optode respirometry (for details see Köster et al., 2008) with a 10-channel optode respirometer (PreSens Precision Sensing Oxy-10 Mini, Regensburg, Germany) under simulated in situ conditions in temperature-controlled refrigerators. Experiments were run in gas-tight glass bottles (12-13 ml). For each set of experiments, two controls without animals were measured under exactly the same conditions to compensate for potential bias. The number of animals per bottle depended on the copepods size, stage and metabolic activity. Animals were not fed during the experiments but they showed natural species-specific movements. Immediately after the experiments, all specimens were deep-frozen at - 80 °C for later dry mass determination (after lyophilisation for 48 h) in the home lab. The carbon content (% of dry mass) of each species was measured by mass-spectrometry in association with stable isotope analysis and body dry mass was converted to units of carbon. For species without available carbon data, the mean value of all copepod species (44% dry mass) was applied. For the estimation of carbon requirements of copepod species, individual oxygen consumption rates were converted to carbon units, assuming that the expiration of 1 ml oxygen mobilises 0.44 mg of organic carbon by using a respiratory quotient (RQ) of 0.82 for a mixed diet consisting of proteins (RQ = 0.8-1.0), lipids (RQ = 0.7) and carbohydrates (RQ = 1.0) (Auel and Werner, 2003). The carbon ingestion rates were calculated using the energy budget and the potential maximum ingestion rate approach. To allow for physiological comparisons of respiration rates of deep- and shallow-living copepod species without the effects of ambient temperature and different individual body mass, individual respiration rates were temperature- (15°C, Q10=2) and size-adjusted. The scaling coefficient of 0.76 (R2=0.556) is used for the standardisation of body dry mass to 0.3 mg (mean dry mass of all analysed copepods), applying the allometric equation R= (R15°C/M0.76)×0.30.76, where R is respiration and M is individual dry mass in mg.

(Supplemet S1) Silicon oxide and Potassium + Sodium oxide from the PACManus hydrothermal area

This study presents a systematic analysis and interpretation of autonomous underwater vehicle-based microbathymetry combined with remotely operated vehicle (ROV) video recordings, rock analyses and temperaturemeasurements within the PACManus hydrothermal area located on Pual Ridge in the Bismarck Sea of eastern Manus Basin. The data obtained during research cruise Magellan-06 and So-216 provides a framework for understanding the relationship between the volcanism, tectonismand hydrothermal activity. PACManus is a submarine felsic vocanically-hosted hydrothermal area that hosts multiple vent fields locatedwithin several hundredmeters of one another but with different fluid chemistries, vent temperatures and morphologies. The total area of hydrothermal activity is estimated to be 20,279m**2. Themicrobathymetrymaps combinedwith the ROV video observations allow for precise high-resolution mapping estimates of the areal extents of hydrothermal activity.We find the distribution of hydrothermal fields in the PACManus area is primarily controlled by volcanic features that include lava domes, thick andmassive blocky lava flows, breccias and feeder dykes. Spatial variation in the permeability of local volcanic facies appears to control the distribution of venting within a field.We define a three-stage chronological sequence for the volcanic evolution of the PACManus based on lava flow morphology, sediment cover and lava SiO2 concentration. In Stage-1, sparsely to moderately porphyritic dacite lavas (68-69.8 wt.% SiO2) erupted to form domes or cryptodomes. In Stage-2, aphyric lava with slightly lower SiO2 concentrations (67.2-67.9 wt.% SiO2) formed jumbled and pillowed lava flows. In the most recent phase Stage-3, massive blocky lavaswith 69 to 72.5wt.% SiO2were erupted throughmultiple vents constructing a volcanic ridge identified as the PACManus neovolcanic zone. The transition between these stages may be gradual and related to progressive heating of a silicic magma following a recharge event of hot, mantle-derived melts.

Mesozooplankton community development at elevated CO2

The increasing CO2 concentration in the atmosphere caused by burning fossil fuels leads to increasing pCO2 and decreasing pH in the world ocean. These changes may have severe consequences for marine biota, especially in cold-water ecosystems due to higher solubility of CO2. However, studies on the response of mesozooplankton communities to elevated CO2 are still lacking. In order to test whether abundance and taxonomic composition change with pCO2, we have sampled nine mesocosms, which were deployed in Kongsfjorden, an Arctic fjord at Svalbard, and were adjusted to eight CO2 concentrations, initially ranging from 185 µatm to 1420 µatm. Vertical net hauls were taken weekly over about one month with an Apstein net (55 µm mesh size) in all mesocosms and the surrounding fjord. In addition, sediment trap samples, taken every second day in the mesocosms, were analysed to account for losses due to vertical migration and mortality. The taxonomic analysis revealed that meroplanktonic larvae (Cirripedia, Polychaeta, Bivalvia, Gastropoda, and Decapoda) dominated in the mesocosms while copepods (Calanus spp., Oithona similis, Acartia longiremis and Microsetella norvegica) were found in lower abundances. In the fjord copepods prevailed for most of our study. With time, abundance and taxonomic composition developed similarly in all mesocosms and the pCO2 had no significant effect on the overall community structure. Also, we did not find significant relationships between the pCO2 level and the abundance of single taxa. Changes in heterogeneous communities are, however, difficult to detect, and the exposure to elevated pCO2 was relatively short. We therefore suggest that future mesocosm experiments should be run for longer periods.