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EARTH SCIENCE | BIOSPHERE | ECOSYSTEMS | MARINE ECOSYSTEMS | COASTAL | KELP FOREST

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    Out-of-range observations of significant rafts of giant kelp (Macrocystis pyrifera) washing ashore in southern NSW in winter 2020. On 9 August 2020, two local marine naturalists on the south coast of New South Wales, Australia noticed a significant amount of a large unfamiliar kelp washed up on a local beach. Following some quick confirmations via phone and email, it was revealed that the unfamiliar seaweed was giant kelp (Macrocystis pyrifera): a species whose closest known populations are ~450 km away to the south (in Tasmania and western Victoria) and whose transport to New South Wales would have required oceanic rafting over several weeks and hundreds of kilometres against the prevailing south-flowing East Australian Current. Subsequent community-led searches over the following days confirmed four more locations of often-substantial amounts of giant kelp wrack, as well as many more anecdotal and unconfirmed accounts.

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    Kelps are in global decline due to climate change, including ocean warming. To identify vulnerable species, we need to identify their tolerances to increasing temperatures and whether tolerances are altered by co-occurring drivers such as inorganic nutrient levels. This is particularly important for those with restricted distributions, which may already be experiencing thermal stress. To identify thermal tolerance of the range restricted kelp Lessonia corrugata, we conducted a laboratory experiment on juvenile sporophytes to measure performance (growth, photosynthesis) across its thermal range (4 – 22 °C). We found the upper thermal limit for growth and photosynthesis to be ~ 22 – 23 °C, with an optimum of ~ 16 °C. To determine if elevated inorganic nitrogen availability could enhance thermal tolerance, we compared performance of juveniles under low (4.5 µmol/day) and high (90 µmol/day) nitrate conditions at and above the thermal optimum (16 – 23.5 °C). Nitrate enrichment did not enhance thermal performance at temperatures above the optimum but did lead to elevated growth rates at the thermal optimum 16 °C. Our findings indicate L. corrugata is likely to be extremely susceptible to moderate ocean warming and marine heatwaves. Peak sea surface temperatures during summer in eastern and northeastern Tasmania can reach up to 20 – 21 °C and climate projections suggest that L. corrugata’s thermal limit will be regularly exceeded by 2050 as south-eastern Australia is a global ocean-warming hotspot. By identifying the upper thermal limit of L. corrugata we have taken a critical step in predicting the future of the species in a warming climate.

  • Observational data for the Kelp Ecosystem Ecology Network. These data come from transects of rocky reefs taken around the world using the KEEN observational data protocol (see http://kelpecosystems.org for full description of methods and handbook). See “How” for methods. Briefly, the observational data consists of the following components, all included here: site information, fish observations, quadrat sampling, band transect sampling, percent cover from uniform point counts, and kelp morphometrics. Data Files Data files included and what they contain are as follows: keen_sites.csv - Physical and locational data for all KEEN sites and transect. keen_cover.csv - Percent cover of sessile algae and invertebrates. keen_fish.csv - Counts of fish by size class along a transect. keen_quads.csv - Counts of common algae, sessile invertebrates, and demersal fish that can be individuated. keen_swath.csv - Counts of rarer algae, sessile invertebrates, and demersal fish that can be individuated. Data Use To use the observational data here for published work we ask that 1) You contact the network coordinator, jarrett.byrnes@umb.edu, and notify them of your intention so that we can coordinate among any ongoing projects using the same data, 2) if the data has not been used in a publication in the literature before, we request that you reach out to the PIs responsible for the data you will be using and engage in a conversation about co-authorship, 3) if it has been used previously, merely cite the datasets associated with each PI that you use. The references are listed below. For access to the entire data cleaning and processing pipeline, see https://github.com/kelpecosystems/observational_data. For access to scans of the original data sheets, contact jarrett.byrnes@umb.edu. ------------------------------------------------------ For general methods: Byrnes, Jarrett E.K., Haupt, Alison J., Reed, Daniel C., Wernberg, Thomas., Pérez-Matus, Alejandro., Shears, Nick T., Konar, Brenda, Gagnon, Pat, and Vergés, Adriana. 2014. Kelp Ecosystem Ecology Network Monitoring Handbook. Kelp Ecosystem Ecology Network. For specific data sets, use the following, but also include date accessed from TemperateReefBase in order to track which version of the data you are using. Byrnes, Jarrett E.K., Haupt, Alison J., Lyman, Ted. 2014. Kelp forest communities at Appledore Island, the Boston Harbor Islands, and Salem Sound. Kelp Ecosystem Ecology Network. Dijkstra, Jennifer A., Mello, Kristen. 2015. Kelp forest communities at York, Maine. Kelp Ecosystem Ecology Network. Grabwoski, Jonathan and MacMahan, Marissa. 2015. Kelp forest communities in Nahant, Massachusetts, and Pemaquid, Maine. Kelp Ecosystem Ecology Network. Humphries Austin T., Paight C, Ben-Horin Tal, Green Lindsay, Thornber, Carol. 2016. Kelp forest communities in Narragansett Bay, Rhode Island. Kelp Ecosystem Ecology Network. Rasher, Douglass and Price, Nicole. 2017. Kelp forest communities of central and downeast Maine. Kelp Ecosystem Ecology Network. Peréz-Matus, Alejandro and Shaughnessy, Brianna. 2017. Kelp forest communities of central and northern Chile. Kelp Ecosystem Ecology Network.

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    Biogenic marine habitats are increasingly threatened by a multitude of human impacts, and temperate coasts in particular are exposed to progressively more intense and frequent anthropogenic stressors. In this study, the single and multiple effects of the urban stressors of nutrification and sedimentation on kelp bed communities were examined within Australia’s largest urbanised embayment (Port Phillip Bay, Victoria). Within this system, grazing by sea urchins (Heliocidaris erythrogramma) plays an important role in structuring reef communities by overgrazing kelp beds and maintaining an alternative and stable urchin barrens state. It is therefore important to explore the effects of urban stressors on kelp bed dynamics related to urchin abundance, and test the relative strengths of bottom-up and / or physical drivers (e.g. elevated nutrients and sediment) versus top-down (e.g. urchin grazing) forces on kelp bed community structure. The interactions of these drivers were assessed to determine whether their combination has synergistic, antagonistic, or additive effects on kelp beds. It was found that kelp responds positively to nutrient enhancement, but when combined with enhanced abundance of grazing sea urchins, the local positive effect of nutrient enhancement is overwhelmed by the negative effect of increased herbivory. Turf-forming algae behaved very differently, showing no detectable response to nutrification, yet showing a positive response to urchins, apparently mediated by overgrazing of canopy-forming algae that limit turf development. No direct effects of enhanced sediment load (at twice the ambient load) were found on intact kelp beds. Collectively, the results demonstrate that the ‘top-down’ control of urchin grazing locally overwhelms the positive ‘bottom-up’ effect of nutrient enhancement, and that intact kelp beds demonstrate resilience to direct impacts of urban stressors.

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    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.

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    The abundance of macroinvertebrates associated with 28 experimental artificial reefs supporting different patch sizes and density of kelp (Ecklonia radiata) off Maria Island, Tasmania. Macroinvertebrates were assessed by diver-based visual census conducted between November 2015 and December 2016. This data was collected to examine how the patch size and density of kelp influences the establishment of macroinvertebrate assemblages.

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    The recruitment of mussels and microphytobenthic (MPB) algae to 28 experimental artificial reefs supporting different patch sizes and density of kelp (Ecklonia radiata) off Maria Island, Tasmania. The recruitment of mussels was assessed using rope fibre habitats, and the recruitment of MPB algae was assessed using microscope slides, positioned across the artificial reef and collected in November 2015. These data were collected to examine how the patch size and density of kelp influences the establishment of MPB algae and mussels.

  • This dataset comes from the Floating Forests project (http://floatingforests.org). Floating Forests is an online citizen science project attempting to map the cover of surface-canopy forming kelps, primarily the giant kelp Macrocystis pyrifera, using Landsat data. To acquire the data, citizen scientists were given tiles of images taken from the Landsat series of satellites (https://landsat.usgs.gov/) scenes that had been manipulated to make kelp more visible. Landsat has a roughly two week repeat time for the entire globe and a 30m resolution, although given variability in weather quarterly aggregation is recommended. Each image was scene at minimum four times. If no kelp was noted, then it was retired and scored as a zero. If kelp was noted in the first four classifications, then an individual image was shown to fifteen people total. The polygons of kelp beds presented here represent consensus classifications from the platform and are tagged with minimum number of users who classified pixels in the polygons as kelp. For example, at the five user threshold, each area represents pixels where at least five users - not neccesarily the same five users - said there was kelp present. This consensus classification has been shown to match very closely to expert classifications. For more information and links to outputs, see http://blog.floatingforests.org in addition to the main project site. Or go to the main project site, and start a conversation in the "talk" section of the site.

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    Data accompanying Layton et al. 2019, Resilience and stability of kelp forests: the importance of patch dynamics and environment-engineer feedbacks. PLOS ONE. To explore how resilience and stability of kelp habitats is influenced by this habitat degradation, we created an array of patch reefs of various sizes and supporting adult Ecklonia radiata kelp transplanted at different densities. This enabled testing of how sub-canopy abiotic conditions change with reductions in patch size and adult kelp density, and how this influenced demographic processes of microscopic and macroscopic juvenile kelp.

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    -- Layton et al. Chemical microenvironments within macroalgal assemblages: implications for the inhibition of kelp recruitment by turf algae. Limnology & Oceanography. DOI:10.1002/lno.11138 -- Kelp forests around the world are under increasing pressure from anthropogenic stressors. A widespread consequence is that in many places, complex and highly productive kelp habitats have been replaced by structurally simple and less productive turf algae habitats. Turf algae habitats resist re-establishment of kelp via recruitment inhibition; however little is known about the specific mechanisms involved. One potential factor is the chemical environment within the turf algae and into which kelp propagules settle and develop. Using laboratory trials, we illustrate that the chemical microenvironment (O2 concentration and pH) 0.0–50 mm above the benthos within four multispecies macroalgal assemblages (including a turf-sediment assemblage and an Ecklonia radiata kelp-dominated assemblage) are characterised by elevated O2 and pH relative to the surrounding seawater. Notably however, O2 and pH were significantly higher within turf-sediment assemblages than in kelp-dominated assemblages, and at levels that have previously been demonstrated to impair the photosynthetic or physiological capacity of kelp propagules. Field observations of the experimental assemblages confirmed that recruitment of kelp was significantly lower into treatments with dense turf algae than in the kelp-dominated assemblages. We demonstrate differences between the chemical microenvironments of kelp and turf algae assemblages that correlate with differences in kelp recruitment, highlighting how degradation of kelp habitats might result in the persistence of turf algae habitats and the localised absence of kelp.