We compare the formulation and emergent dynamics of 11 CMIP6 IPCC marine biogeochemical models. We find that the largest source of uncertainty across model simulations of marine carbon cycling is grazing pressure (i.e. the phytoplankton specific loss rate to grazing). Variability in grazing pressure is driven by large differences in zooplankton specific grazing rates, which are not sufficiently compensated for by offsetting differences in zooplankton specific mortality rates. Models instead must tune the turnover rate of the phytoplankton population to balance large differences in top-down grazing pressure and constrain net primary production. We then run a controlled sensitivity experiment in a global, coupled ocean-biogeochemistry model to test the sensitivity of marine carbon cycling to this uncertainty and find that even when tuned to identical net primary production, export and secondary production remain extremely sensitive to grazing, likely biasing predictions of future climate states and food security.

Antarctic krill (Euphausia superba) have a keystone role in the Southern Ocean, as the primary prey of Antarctic predators. Any decreases in krill abundance could result in a major ecological regime shift, but there is currently limited information on how climate change may affect krill. Increasing anthropogenic carbon dioxide (CO2) emissions are causing ocean acidification, as absorption of atmospheric CO2 in seawater alters ocean chemistry. Ocean acidification increases mortality and negatively affects physiological functioning in some marine invertebrates, and is predicted to occur most rapidly at high latitudes. Here we show that, in the laboratory, adult krill are able to survive, grow, store fat, mature, and maintain respiration rates when exposed to near-future ocean acidification (1000 – 2000 μatm pCO2) for one year. Despite differences in seawater pCO2 incubation conditions, adult krill are able to actively maintain the acid-base balance of their body fluids in near-future pCO2, which enhances their resilience to ocean acidification.

Antarctic krill (Euphausia superba) are a keystone species in the Southern Ocean, but little is known about how they will respond to climate change. Ocean acidification, caused by sequestration of carbon dioxide into ocean surface waters (pCO2), is known to alter the lipid biochemistry of some organisms. This can have cascading effects up the food chain. In a year-long laboratory experiment adult krill were exposed to ambient seawater pCO2 levels (400 μatm), elevated pCO2 levels that mimicked near-future ocean acidification (1000, 1500 and 2000 μatm) and an extreme pCO2 level (4000 μatm). The laboratory light regime mimicked the seasonal Southern Ocean photoperiod and krill received a constant food supply. Total lipid mass (mg g -1 DM) of adult krill was unaffected by near-future levels of seawater pCO2. Fatty acid composition (%) and fatty acid ratios associated with immune responses and cell membrane fluidity were also unaffected by near-future pCO2, apart from an increase in 18:3n-3/18:2n-6 ratios in krill in 1500 μatm pCO2 in winter and spring. Extreme pCO2 had no effect on krill lipid biochemistry during summer. During winter and spring, krill in extreme pCO2 had elevated levels of omega-6 fatty acids (up to 1.2% increase in 18:2n-6, up to 0.8% increase in 20:4n-6 and lower 18:3n-3/18:2n-6 and 20:5n-3/20:4n-6 ratios), and showed evidence of increased membrane fluidity (up to three-fold increase in phospholipid/sterol ratios). These results indicate that the lipid biochemistry of adult krill is robust to near-future ocean acidification.

Collection of processed BGC-Argo float profiles, used to calculate phytoplankton phenology from chlorophyll, phytoplankton carbon and nitrate.

Mesozooplankton community composition and structure were examined throughout the D’Entrecasteaux Channel, Huon Estuary and North West Bay, Tasmania, from November 2004 to October 2005, the data represented by this record was collected on the 13/10/2005. The composition of the mesozooplankton community was typical of inshore, temperate marine habitats, with seasonally higher abundance in summer and autumn and lower numbers in winter and spring. Copepods were the largest contributors to total abundance across all seasons and stations, while cladocerans and appendicularians were proportionally abundant in spring and summer. The faecal pellets of these three main groups, along with those of krill and amphipods, also contributed significantly to material recovered from sediment traps. Meroplanktonic larvae of benthic animals showed short-term peaks in abundance and were often absent from the water column for long periods. Spatially, North West Bay and the Channel had a higher representation of typically marine species, including Calanus australis and Labidocera cervi, while truly estuarine species, such as the copepod Gladioferens pectinatus, were more important in the Huon Estuary.

These files contain the data recorded from a mesocosm experiment conducted in Bergen, Norway 2022 which assessed the effect of simualted mineral-based (silicate or calcium) ocean alkalinity enhancement (OAE) on diatom silicification. Ten mesocosms were used in total, divided into two groups either the silicate- or calcium based group and alkalinity was increased by either 0, 150, 300, 450 or 600 µmol L-1 above natrually occuring levels. The PDMPO-fluorescence (an appropriate proxy for silicification) of diatoms was recorded on eight seperate days during the experiment. Accompanying data includes measured; macronutrients (nitrate, nitrite, phophate, silicate), total alkalinity, biogenic silica in the water column and sediment trap.

The fatty acid content and composition of the Antarctic krill Euphausia superba Dana, 1850 were investigated using samples collected by a commercial fishing vessel. This dataset allowed comparison between seasons, years (2013–2016), and different fishing locations. Quantities of omega 3 fatty acids 20:5n-3 and 22:6n-3 (mg/g dry mass; DM) were highest in autumn and decreased through winter to reach a spring low. Quantities of the flagellate marker 18:4n-3 and diatom marker 16:1n-7c were variable and did not display the same seasonal fluctuations. In summer, krill had high percentages (% total fatty acids) of 20:5n-3 and 22:6n-3, total PUFA, and low 18:1n-9c/18:1n-7c ratios, indicating a more herbivorous diet. Krill became more omnivorous from autumn to spring, indicated by increasing ratios of 18:1n-9c/18:1n-7c and percentages of Σ 20:1 + 22:1 isomers. Bacterial fatty acids (Σ C15 + C17 + C19 isomers) were minor components year-round (0.9–1.8 %). Seasonal levels of herbivory and omnivory differed between years, and levels of specific fatty acid ratios differed between fishing locations. The fatty acid 18:4n-3 was a major driver of variability in krill fatty acid composition, with no obvious seasonal driver. This is the first study to report krill fatty acid data during all four seasons over consecutive years. This large-scale study highlights the value of using fisheries samples to examine seasonal and annual fluctuations in krill diet and condition.

Data collected from Southern Ocean phytoplankton laboratory culture experiments to examine the effect of iron limitation on the Chlorophyll fluorescence (F) to chlorophyll (Chl) ratio. Irradiance levels at which cultures were grown are indicated by the photon flux density (PFD). Growth rates of Fe limited cultures (-Fe) relative to Fe replete cultures (+Fe) are referred to as μ / μmax (unitless).