Data were collected from 28 artificial reefs varying in size and supporting different densities of transplanted kelp (Ecklonia radiata). We used rope fibre habitats (RFHs) attached to the benthos of the reefs and destructive sampling of understory algae to collect data on epifaunal invertebrates that naturally colonised the reefs (e.g. secondary productivity, species richness, Shannon diversity). The goal of the research was to understand how kelp structure influences the biodiversity and secondary productivity of epifauna.

This record provides an overview of the scope and research output of NESP Marine Biodiversity Hub Project A14 - "Identification of near-shore habitats of juvenile white sharks in Southwestern Australia". For specific data outputs from this project, please see child records associated with this metadata. -------------------- In early 2018, the CSIRO provided the first estimate of abundance for the southern-western adult white shark. Establishing an estimate of total abundance was not possible due to the lack of information of the juvenile life history stage in south-western Australia. The estimate of adult abundance also included trend (essentially zero or slightly negative), however, it was noted that to confirm the trend, a further decade of sampling would be required. This can be reduced if we identify near-shore habitats where juvenile white sharks from the southern-western population can be readily accessed. This pilot project will investigate credible anecdotal evidence of juvenile white sharks using near-shore habitat near the head of the Great Australia Bight, and inform future project development steps. The pilot project will include collaboration and the opportunity for capacity building with the Yatala Land Management group. The outcome of this pilot project will inform whether or not to proceed to future (on-water) activities. Planned Outputs • Spatial maps showing juvenile white-shark aggregation areas that include Australian marine park boundaries and zoning in jpeg format • Shapefile of juvenile white-shark aggregation areas provided to ERIN • High quality and project relevant images (still and video) suitable for communications purposes • Summary (and images) of opportunistic wildlife observations within the Great Australian Bight Marine Park (Commonwealth waters) • Final report

Sea urchins have the capacity to destructively overgraze kelp beds and cause a wholesale shift to an alternative and stable ‘urchin barren’ state. However, their destructive grazing behaviour can be highly labile and contingent on behavioural shifts at the individual and local population level. Changes in supply of allochthonous food sources, i.e. availability of drift-kelp, is often suggested as a proximate trigger of change in sea urchin grazing behaviour, yet field tests of this hypothesis are rare. Here we conduct a suite of in situ behavioural surveys and manipulative experiments within kelp beds and on urchin barrens to examine foraging movements and evidence for a behavioural switch to an overgrazing mode by the Australian sea urchin Heliocidaris erythrogramma (Echinometridae). Tracking of urchins using time-lapse photography revealed urchin foraging to broadly conform to a random-walk-model within both kelp beds and on barren grounds, while at the individual level there was a tendency towards local ‘homing’ to proximate crevices. However, consistent with locally observed ‘mobile feeding fronts’ that can develop at the barrens-kelp interface, urchins were experimentally inducible to show directional movement toward newly available kelp. Furthermore, field assays revealed urchin grazing rates to be high on both simulated drift-kelp and attached kelp thalli on barren grounds, however drift-kelp but not attached kelp was consumed at high rates within kelp beds. Time-lapse tracking of urchin foraging before/ after the controlled addition of drift-kelp on barrens revealed a reduction in foraging movement across the reef surface when drift-kelp was captured. Collectively results indicate that the availability of drift-kelp is a pivotal trigger in determining urchin feeding modes, which is demonstrably passive and cryptic in the presence of a ready supply of drift-kelp. Recovery of kelp beds therefore appears possible if a sustained influx of drift-kelp was to inundate urchin barrens, particularly on reefs where local urchin densities and where grazing pressure is close to the threshold enabling kelp bed recovery.

Google Earth KMZ files of hammerhead sharks tagged with Wildlife Computers miniPAT archival tags and SPOT6 tags. Files of animals tagged with MiniPAT tags include an MELE polygon, which is the 'Maximum extent of location estimates', that is, a polygon enclosing all position estimates at the maximum error level (100 km). Collectively, movements are restricted within state waters with no hammerheads moving across state or International boundaries.

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.

Rock samples were dredged from seamounts in the southern Tasman Sea on the RV Investigator, voyage IN2018_V08

Phytoplankton productivity in the polar Southern Ocean (SO) plays an important role in the transfer of carbon from the atmosphere to the ocean’s interior, a process called the biological carbon pump, which helps regulate global climate. SO productivity in turn is limited by low iron, light, and temperature, which restrict the ef- ficiency of the carbon pump. Iron and light can colimit productivity due to the high iron content of the photosynthetic photosystems and the need for increased photosystems for low-light acclimation in many phytoplankton. Here we show that SO phytoplankton have evolved critical adaptations to enhance photosynthetic rates under the joint constraints of low iron, light, and temperature. Under growth-limiting iron and light levels, three SO species had up to sixfold higher photosynthetic rates per photosystem II and similar or higher rates per mol of photosynthetic iron than tem- perate species, despite their lower growth temperature (3 vs. 18 °C) and light intensity (30 vs. 40 μmol quanta·m2·s−1), which should have decreased photosynthetic rates. These unexpectedly high rates in the SO species are partly explained by their unusually large photosynthetic antennae, which are among the largest ever recorded in marine phytoplankton. Large antennae are disadvan- tageous at low light intensities because they increase excitation energy loss as heat, but this loss may be mitigated by the low SO temperatures. Such adaptations point to higher SO production rates than environmental conditions should otherwise permit, with implications for regional ecology and biogeochemistry.