Turning on the heat: ecological response to simulated warming in the sea

Significant warming has been observed in every ocean, yet our ability to predict the consequences of oceanic warming on marine biodiversity remains poor. Experiments have been severely limited because, until now, it has not been possible to manipulate seawater temperature in a consistent manner across a range of marine habitats. We constructed a "hot-plate'' system to directly examine ecological responses to elevated seawater temperature in a subtidal marine system. The substratum available for colonisation and overlying seawater boundary layer were warmed for 36 days, which resulted in greater biomass of marine organisms and a doubling of space coverage by a dominant colonial ascidian. The "hot-plate'' system will facilitate complex manipulations of temperature and multiple stressors in the field to provide valuable information on the response of individuals, populations and communities to environmental change in any aquatic habitat

Substantial blue carbon in overlooked Australian kelp forests

Recognition of the potential for vegetated coastal ecosystems to store and sequester carbon has led to their increasing inclusion into global carbon budgets and carbon offset schemes. However, kelp forests have been overlooked in evaluations of this ‘blue carbon’, which have been limited to tidal marshes, mangrove forests, and seagrass beds. We determined the continental-scale contribution to blue carbon from kelp forests in Australia using areal extent, biomass, and productivity measures from across the entire Great Southern Reef. We reveal that these kelp forests represent 10.3–22.7 Tg C and contribute 1.3–2.8 Tg C year−1 in sequestered production, amounting to more than 30% of total blue carbon stored and sequestered around the Australian continent, and ~ 3% of the total global blue carbon. We conclude that the omission of kelp forests from blue carbon assessments significantly underestimates the carbon storage and sequestration potential from vegetated coastal ecosystems globally

Editorial: advances in understanding marine heatwaves and their impacts

© The Author(s), 2020. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Benthuysen, J. A., Oliver, E. C. J., Chen, K., & Wernberg, T. Editorial: advances in understanding marine heatwaves and their impacts. Frontiers in Marine Science, 7, (2020): 147, doi:10.3389/fmars.2020.00147.Editorial on the Research Topic Advances in Understanding Marine Heatwaves and Their Impacts In recent years, prolonged, extremely warm water events, known as marine heatwaves, have featured prominently around the globe with their disruptive consequences for marine ecosystems. Over the past decade, marine heatwaves have occurred from the open ocean to marginal seas and coastal regions, including the unprecedented 2011 Western Australia marine heatwave (Ningaloo Niño) in the eastern Indian Ocean (e.g., Pearce et al., 2011), the 2012 northwest Atlantic marine heatwave (Chen et al., 2014), the 2012 and 2015 Mediterranean Sea marine heatwaves (Darmaraki et al., 2019), the 2013/14 western South Atlantic (Rodrigues et al., 2019) and 2017 southwestern Atlantic marine heatwave (Manta et al., 2018), the persistent 2014–2016 “Blob” in the North Pacific (Bond et al., 2015; Di Lorenzo and Mantua, 2016), the 2015/16 marine heatwave spanning the southeastern tropical Indian Ocean to the Coral Sea (Benthuysen et al., 2018), and the Tasman Sea marine heatwaves in 2015/16 (Oliver et al., 2017) and 2017/18 (Salinger et al., 2019). These events have set new records for marine heatwave intensity, the temperature anomaly exceeding a climatology, and duration, the sustained period of extreme temperatures. We have witnessed the profound consequences of these thermal disturbances from acute changes to marine life to enduring impacts on species, populations, and communities (Smale et al., 2019). These marine heatwaves have spurred a diversity of research spanning the methodology of identifying and quantifying the events (e.g., Hobday et al., 2016) and their historical trends (Oliver et al., 2018), understanding their physical mechanisms and relationships with climate modes (e.g., Holbrook et al., 2019), climate projections (Frölicher et al., 2018), and understanding the biological impacts for organisms and ecosystem function and services (e.g., Smale et al., 2019). By using sea surface temperature percentiles, temperature anomalies can be quantified based on their local variability and account for the broad range of temperature regimes in different marine environments. For temperatures exceeding a 90th-percentile threshold beyond a period of 5-days, marine heatwaves can be classified into categories based on their intensity (Hobday et al., 2018). While these recent advances have provided the framework for understanding key aspects of marine heatwaves, a challenge lies ahead for effective integration of physical and biological knowledge for prediction of marine heatwaves and their ecological impacts. This Research Topic is motivated by the need to understand the mechanisms for how marine heatwaves develop and the biological responses to thermal stress events. This Research Topic is a collection of 18 research articles and three review articles aimed at advancing our knowledge of marine heatwaves within four themes. These themes include methods for detecting marine heatwaves, understanding their physical mechanisms, seasonal forecasting and climate projections, and ecological impacts.We thank the contributing authors, reviewers, and the editorial staff at Frontiers in Marine Science for their support in producing this issue. We thank the Marine Heatwaves Working Group (http://www.marineheatwaves.org/) for inspiration and discussions. This special issue stemmed from the session on Advances in Understanding Marine Heat Waves and Their Impacts at the 2018 Ocean Sciences meeting (Portland, USA)

Missing the marine forest for the trees

Seascapes dominated by large, structurally complex seaweeds are ubiquitous. These critical ecosystems are under increasing pressure from human activities, and conceiving successful management strategies to ensure their persistence and/or recovery is of paramount importance. Currently, ecosystems dominated by large seaweeds are referred to as either ‘forests’ or ‘beds’. We demonstrate how this dual terminology is confusing, is used inconsistently, and reduces the efficiency of communication about the importance and perils of seaweed habitats. As a consequence, it undermines work to alleviate and mitigate their loss and impedes research on unifying principles in ecology. We conclude that there are clear benefits of simply using the more intuitive term ‘forest’ to describe all seascapes dominated by habitat-forming seaweeds. This is particularly true as researchers scramble to reconcile ecological functions and patterns of change across disparate regions and species to match the increasingly global scale of environmental forcing on these critical ecosystem

Subtidal macroalgal richness, diversity and turnover, at multiple spatial scales, along the southwestern Australian coastline

Patterns of species richness are governed by processes that act at vastly different spatial scales. In the marine system of southwest Australia, macroalgal assemblage structure and richness is thought to be strongly influenced by both the Leeuwin Current, which acts at large regional spatial scales, and small-scale processes such as competition, wave disturbance and habitat heterogeneity. We examined macroalgal species richness and diversity at multiple spatial scales using a three-factor hierarchal design. Spatial extents ranged from metres (between quadrats) to many hundreds of kilometres (between regions), and the study encompassed almost 2000 km of temperate coastline. Macroalgal assemblages were highly speciose and the number, identity, and diversity of species varied considerably at all spatial scales. Small scale variability, at the scale of site or quadrat, contributed most to total variation in species richness and diversity, suggesting that small-scale processes are important drivers of ecological pattern in this system. Species richness, diversity and taxonomic distinctness increased sequentially along the coastline, from warmer to cooler waters. Small scale variability was most likely maintained by wave disturbance and habitat heterogeneity at these scales, while regional scale diversity and richness clines were attributed to the fact that most species had cool-water affinities and the southern coast of Australia is a hotspot of floral speciation and diversity. Macroalgal assemblages in southwest Australia are speciose and largely endemic, and biodiversity patterns are structured by multiple processes operating at multiple spatial scale

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Recovery of algal turfs following removal

As a consequence of the increasing human footprint on the environment, marine ecosystems are rapidly transforming into new configurations dominated by early-successional and weedy life forms. Algal turfs, in particular, are emerging as a common and widespread configuration of shallow temperate and tropical reefs, and are predicted to transform reef dynamics and ecosystem services. Restoration is an increasingly used approach to mitigate these transformations, with turf removal being proposed as a tool to shift back the competitive balance and facilitate the recovery of initial species, such as forest-forming seaweeds. Yet, our practical understanding of turf recovery trajectories following removal is limited, and removal success may be hindered by strong feedback mechanisms that reinforce turf dominance once turfs are established. Here we investigate the recovery of algal turfs and their properties (mean height, turf biomass and sediment load) to experimental clearance across six turf-dominated reefs at ca. 9 m in subtropical western Australia. Turf cover, mean height, and sediment loads exhibited a rapid recovery following experimental clearing, with all experimental sites reaching pre-clearing turf conditions between 28 and 46 days. This response was mostly driven by the growth of filamentous turf species, whose cover exhibited a positive relationship with sediment load, and are well-known to rapidly recover after disturbance. Turf abundance and turf properties remained relatively constant for the remaining experimental period. Our results suggest that clearing turfs creates only a small time window for recovery of seaweed forests, which limits the effectiveness of turf clearing as a restoration tool. System-specific quantitative evidence on the recovery capacity of turfs may thus be necessary to guide restoration initiatives and develop decision support systems that account for the risks, feasibility, and costs and benefits of restoring turf-dominated systems to previous configurations.publishedVersio

Assemblage turnover and taxonomic sufficiency of subtidal macroalgae at multiplespatial scales

Spatial variability in the structure of subtidal macroalgal assemblages in southwest Australia was examined at multiple spatial scales using a three-factor hierarchal design. Spatial extents ranged from metres (between quadrats) to many hundreds of kilometres (between regions), and the study encompassed N2000 km of temperate coastline. In addition, the influence of taxonomic resolution, from species level data to class level, on spatial patterns was investigated to assess the potential evolutionary timescales of the pattern and for developing cost effective regionally applicable surrogates for biodiversity monitoring. Almost 300 species were identified from 14 sites, representing considerable biodiversity and a significant subset of the total benthic macroalgal diversity in the region (∼1000 species). Multivariate variability was significant at all spatial scales examined, but most prominent at smallest spatial scales, regardless of taxonomic resolution. Assemblage and species turnover was pronounced at scales of metres to hundreds of metres. Generally, small scale patchiness was a ubiquitous pattern for all individual taxa examined, regardless of taxonomic resolution, while variability at the scale of 10s of km was less important. Even so, differences in spatial variability between taxa were observed, and ecological and historical reasons for such differences are proposed. Taxonomic aggregation to family level had minimal effect on spatial patterns, but aggregation to order level led to changes in some aspects of patterns of assemblage structure. The unique and speciose macroalgal assemblages on subtidal reefs in southwest Australia are shaped by a complex array of historical and contemporary processes that act at multiple spatial (and temporal) scales. Understanding the relative importance of these processes requires that further manipulative and correlative work is conducted across a range of ecologically-important spatial scales

Turban Snails as Habitat for Foliose Algae: Contrasting Geographical Patterns in Species Richness

Understanding patterns of species richness is a major goal for ecologists, especially in space-limited habitats where many organisms live on top of others (epibiosis, e.g. by algae growing on gastropods in marine environments). We tested the hypotheses that species richness of epiflora on the gastropod Turbo torquatus would not differ between regions with similarly rich algal floras, and that epifloral richness would increase with increasing gastropod size. Macroalgal floras of Hamelin Bay (HB), Marmion (M), Jurien Bay (JB) and Kalbarri (K), Western Australia, ranged from ~20 to 40 species reef–1 (JB = HB = M ≥ K). Epiflora on small T. torquatus (shell areacm2) did not differ among regions but epifloral richness increased with increasing basibiont size. Large T. torquatus (\u3e150 cm2) were only found in Hamelin Bay and Marmion, where epifloral richness differed substantially. Epifloral richness was positively related to basibiont size in Marmion but not in Hamelin Bay. However, densities of patellid limpets on large T. torquatus were ~4× higher in Hamelin Bay than in Marmion, implying that limpet grazing suppresses epifloral richness. Epifloral richness on turbinids is not simply associated with regional species pools or gastropod size; rather, biological interactions at the scale of individual basibionts apparently govern broad scale patterns of epibiosis