Graham J. Edgar’s research while affiliated with University of Tasmania and other places

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Publications (286)


Sampled reef sites around Australia. Sites are color coded by tropical (red) and temperate (blue) realms, with point size representing the number of paired day and night surveys conducted at each site, see legend. Broad biogeographical regions are labeled next to associated site clusters.
Community patterns in reef fauna day versus night for fishes (A, B), cryptic fishes (C, D), and invertebrates (E, F) across tropical and temperate regions. Multidimensional Scaling (MDS) ordinations are based on square‐root‐transformed abundance data; day communities are indicated by blue squares; night indicated by black circles. Regions are represented by colored polygons (see legend).
Observed differences in faunal assemblage metrics detected during day and night surveys on tropical and temperate reefs. Richness (A–C); biomass (D–F); and density (G–I) for fishes, cryptic fishes, and invertebrates recorded during day (blue) and night (black) periods across tropical and temperate reefs. Boxplots represent interquartile range (IQR) including median and first (Q1) and third (Q3) quartiles (25th and 75th percentiles), minimum whisker calculated as: Q1–1.5 × IQR, maximum calculated as: Q3 + 1.5 × IQR.
Diel faunal distributions for fishes, cryptic fishes, and invertebrates for tropical and temperate reefs. Mean proportional contribution to overall (A) richness, (B) biomass, and (C) density of faunal groups occurring as exclusively day (blue), exclusively night (black), or occurring in both periods (gray). Boxplots represent interquartile range (IQR) including median and first (Q1) and third (Q3) quartiles (25th and 75th percentiles), minimum whisker calculated as: Q1–1.5 × IQR, maximum calculated as: Q3 + 1.5 × IQR.
Diel distributions of fish trophic groups for tropical and temperate reefs. Richness (A, B), biomass (C, D), and density (E, F) for trophic fish groups recorded during day (blue) and night (black) periods across tropical and temperate reefs. Boxplots represent interquartile range (IQR) including median and first (Q1) and third (Q3) quartiles (25th and 75th percentiles), minimum whisker calculated as: Q1–1.5 × IQR, maximum calculated as: Q3 + 1.5 × IQR.

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Fish and invertebrate communities show greater day–night partitioning on tropical than temperate reefs
  • Article
  • Full-text available

December 2024

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68 Reads

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1 Citation

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Graham J. Edgar

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Diel partitioning of animals within ecological communities is widely acknowledged, yet rarely quantified. Investigation of most ecological patterns and processes involves convenient daylight sampling, with little consideration of the contributions of nocturnal taxa, particularly in marine environments. Here we assess diel partitioning of reef faunal assemblages at a continental scale utilizing paired day and night visual census across 54 shallow tropical and temperate reefs around Australia. Day–night differences were most pronounced in the tropics, with fishes and invertebrates displaying distinct and opposing diel occupancy on coral reefs. Tropical reefs in daytime were occupied primarily by fishes not observed at night (64% of all species sighted across day and night, and 71% of all individuals). By night, substantial emergence of invertebrates not otherwise detected during sunlit hours occurred (56% of all species, and 45% of individuals). Nocturnal emergence of tropical invertebrates corresponded with significant declines in the richness and biomass of predatory and herbivorous diurnal fishes. In contrast, relatively small diel changes in fishes active on temperate reefs corresponded to limited nocturnal emergence of temperate invertebrates. This reduced partitioning may, at least in part, be a result of strong top‐down pressures from fishes on invertebrate communities, either by predation or competitive interference. For shallow reefs, the diel cycle triggers distinct emergence and retreat of faunal assemblages and associated trophic patterns and processes, which otherwise go unnoticed during hours of regular scientific monitoring. Improved understanding of reef ecology, and management of reef ecosystems, requires greater consideration of nocturnal interactions. Without explicit sampling of nocturnal patterns and processes, we may be missing up to half of the story when assessing ecological interactions.

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Latitudinal gradients in herbivorous and detritivorous reef fish productivity

November 2024

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107 Reads

Reviews in Fish Biology and Fisheries

The abundance of herbivorous fishes is known to vary strongly with latitude. However, our understanding of this pattern is largely based on the examination of nominally herbivorous fishes (i.e. both herbivores and detritivores) as a single group. Therefore, we do not know how this collective classification may have confounded our understanding of distribution patterns, nor how different trophic pathways function across latitudes and associated temperature gradients. This constrains our ability to predict how tropicalising reefs may function as oceans warm, especially following range extensions of tropical taxa. Here, we explored the productivity of seven groups of roving nominally herbivorous fishes across eastern (34° of latitude; ~3800 km) and western (23°; ~2600 km) Australia, with specific consideration of the herbivore versus detritivore dichotomy across key spatial and environmental gradients. In terms of the total nominally herbivorous fish community, we found near-continuous declines in species richness with increasing distance from the equator, while total biomass and productivity were maintained across nearly 30° of latitude in eastern Australia. However, when we separated herbivores and detritivores, we found detritivore productivity dominated the tropics but declined abruptly in temperate regions, with this decline closely correlated with decreasing temperature in a synchronous manner along both coastlines. No such synchronous relationship was observed between herbivore productivity and temperature. These results highlight the importance of the herbivore versus detritivore division in understanding reef trophodynamics across latitudes, and the importance of understanding fish-based detritivory when predicting how the trophodynamic functioning of reefs may change along warming coastlines.


Coral responses to a catastrophic marine heatwave are decoupled from changes in total coral cover at a continental scale

October 2024

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119 Reads

The services provided by the world’s coral reefs are threatened by increasingly frequent and severe marine heatwaves. Heatwave-induced degradation of reefs has often been inferred from the extent of the decline in total coral cover, which overlooks extreme variation among coral taxa in their susceptibility and responses to thermal stress. Here, we provide a continental-scale assessment of coral cover changes at 262 shallow tropical reef sites around Australia, using ecological survey data on 404 coral taxa before and after the 2016 mass bleaching event. A strong spatial structure in coral community composition along large-scale environmental gradients largely dictated how coral communities responded to heat stress. While heat stress variables were the best predictors of change in total coral cover, the pre-heatwave community composition best predicted the temporal beta-diversity index (an indicator of change in community composition over time). Indicator taxa in each coral community differed before and after the heatwave, highlighting potential winners and losers of climate-driven coral bleaching. Our results demonstrate how assessment of change in total cover alone may conceal very different responses in community structure, some of which showed strong regional consistency, and may provide a telling outlook of how coral reefs may reorganize in a warmer future.


Limited net poleward movement of reef species over a decade of climate extremes

September 2024

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135 Reads

Nature Climate Change

Warming seas are expected to drive marine life poleward. However, few systematic observations confirm movement among entire communities at both warm and cool range edges. We analysed two continent-scale reef monitoring datasets to quantify changes in latitudinal range edges of 662 Australian shallow-water reef fishes and invertebrates over a decade punctuated by climate extremes. Temperate and tropical species both showed little net movement overall, with retreat often balancing expansion across the continent. Within regions, however, range edges shifted ~100 km per decade, on average, in the poleward or equatorward directions expected from warming or cooling. Although some species responded rapidly to temperature change, we found little evidence for mass poleward migration over the decade. Previous studies based on extreme species observations, rather than tracking all species through time, may have overestimated the prevalence, magnitude and longevity of range shifts amongst marine taxa.


Stock assessment models overstate sustainability of the world's fisheries

August 2024

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220 Reads

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3 Citations

Science

Effective fisheries management requires accurate estimates of stock biomass and trends; yet, assumptions in stock assessment models generate high levels of uncertainty and error. For 230 fisheries worldwide, we contrasted stock biomass estimates at the time of assessment with updated hindcast estimates modeled for the same year in later assessments to evaluate systematic over- or underestimation. For stocks that were overfished, low value, or located in regions with rising temperatures, historical biomass estimates were generally overstated compared with updated assessments. Moreover, rising trends reported for overfished stocks were often inaccurate. With consideration of bias identified retrospectively, 85% more stocks than currently recognized have likely collapsed below 10% of maximum historical biomass. The high uncertainty and bias in modeled stock estimates warrants much greater precaution by managers.


Overcome imposter syndrome: Contribute to working groups and build strong networks

April 2024

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807 Reads

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2 Citations

Biological Conservation

Scientific working groups bring together experts from different disciplines and perspectives to tackle the "wicked problems" facing natural systems and society. Yet participants can feel overwhelmed or inadequate in groups within academic environments, which tends to be most acute at early career stages and in people from systematically marginalized backgrounds. Such feelings can block innovation that would otherwise arise from gaining the full spectrum of unique perspectives, knowledge and skills from a group. Drawing on personal experiences and relevant literature, we identify ten contribution strategies, ranging from generating ideas, analyzing data, and producing visuals to supporting facilitation. Next, we share approaches for an inclusive and supportive process, considering the roles of both participants and leads. Generating the most productive and relevant outcomes from working groups requires engaging the full team in a constructive and supportive environment. We advocate that adopting inclusive approaches that respect the diversity of personality types and perspectives will lead to more innovative solutions to achieve conservation and sustainability goals.


Workflow chart describing the three main steps of our analyses assessing responses to protection of 658 fish species, in terms of occurrence, abundance and biomass. We controlled for habitat, environmental and socioeconomic factors but also spatial autocorrelation. Species‐specific responses were assessed separately for three levels of protection: high (old, and large effective no‐take areas), medium (no‐take areas that did not match age, size, or enforcement criteria) and low protection (all other types of restriction). Step 1: Creation of input data matrices from reef Life Survey; step 2: Modelling the effect of protection on each species occurrence, abundance and biomass; step 3: Testing the influence of traits on species responses using the model estimates from step 2. Colours on the map indicate if the site is protected (orange for protected sites, purple for fished sites).
Boxplots and associated distributions of log‐transformed effect sizes of low, medium and high protection on fish probability of occurrence, abundance and biomass. Each dot represents a single species, and positive values correspond to an increase inside MPAs compared to similar fished areas, while negative values correspond to a decrease. We used log‐transformed data in this plot since the asymmetric distribution of a ratio on the natural scale would not facilitate the visualization of differences.
Models' graphical representation of the interaction between species maximum body length and trophic level in the response to high protection in terms of occurrence probability. Small, medium and large species correspond to species at the 10th, 50th and 90th percentile for maximum body length. Effect sizes are plotted on the natural scale in order to facilitate interpretation of the model outputs: a value of 2 represents a twofold increase inside protected areas compared to outside while controlling for social‐environmental factors and space.
Model's graphical representation of the three‐way interaction between species rarity, trophic level and maximum body length in the effect size of high protection on fish abundance and biomass. Small, medium and large species correspond to species at the 10th, 50th and 90th percentile for maximum body length, and rare, common and very frequent species correspond to the same percentiles in terms of occurrences with yellow, orange and red colours corresponding to very frequent, common and rare species, respectively. Effect sizes are plotted on the natural scale in order to facilitate interpretation of the model outputs: a value of 2 represents a twofold increase inside protected areas compared to outside while controlling for social‐environmental factors and space.
Rarity mediates species‐specific responses of tropical reef fishes to protection

March 2024

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390 Reads

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1 Citation

Ecology Letters

Marine protected areas (MPAs) are the most widely applied tool for marine biodiversity conservation, yet many gaps remain in our understanding of their species‐specific effects, partly because the socio‐environmental context and spatial autocorrelation may blur and bias perceived conservation outcomes. Based on a large data set of nearly 3000 marine fish surveys spanning all tropical regions of the world, we build spatially explicit models for 658 fish species to estimate species‐specific responses to protection while controlling for the environmental, habitat and socio‐economic contexts experienced across their geographic ranges. We show that the species responses are highly variable, with ~40% of fishes not benefitting from protection. When investigating how traits influence species' responses, we find that rare top‐predators and small herbivores benefit the most from MPAs while mid‐trophic level species benefit to a lesser extent, and rare large herbivores experience adverse effects, indicating potential trophic cascades.


The stability framework
Panels illustrate the different components of stability and asynchrony obtained from reef fish abundance data at the community (a) and metacommunity (b–f) levels of organization. Two sites, each including one population of two species, are used throughout to illustrate the derivation of stability and asynchrony measures from timeseries of fish abundance. Stability is indicated as the ratio between the temporal mean and standard deviation of fish abundance (µ/σ), whereas η indicates asynchrony. a Alpha stability, species stability and species asynchrony; μi,j\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$${\mu }_{i,j}$$\end{document} and σi,j\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$${\sigma }_{i,j}$$\end{document} are the temporal mean and standard deviation of species j at site i, respectively. b Average alpha stability (AAS) and spatial community asynchrony (SCA) calculated from total fish abundance between two sites. c Average species stability (ASS) and average species asynchrony (ASA) calculated from the two populations of each species and then averaged between species. d Spatial species asynchrony (SSA) quantified as the average dissimilarity of temporal fluctuations between populations. e Metapopulation stability (MPS) and metapopulation asynchrony (MPAS), calculated from total population abundance and averaged across species. f Gamma stability (GAS) obtained by dividing the temporal mean of total metacommunity abundance by its standard deviation. Arrows pointing to this panel indicate the positive contribution of stability and asynchrony at lower organizational levels to gamma stability. Pink and green ovals indicate whether timeseries were aggregated among species within sites (b, c), among populations in the metacommunity (d) or among metapopulations (e) to derive stability and asynchrony measures. Panels indicate the equations (Eq) used to calculate the various stability and asynchrony measures, which are described in full in Methods.
Timeseries of reef fish abundance and derived measures
a Study sites. b–k Relationships between alpha stability, species stability, species asynchrony, functional richness, and their hypothesized drivers. Data are shown as z-scores for marine protected areas (MPA) and open areas (OA). Panels include the regression parameters estimated from Linear Mixed Effect Models, their significance (2-tailed t-tests; ***p < 0.001; **p < 0.01) and the conditional coefficients of determination (R², indicated only in the first panel for each response variable). Full statistical results are reported in Supplementary Tables 1–3.
Piecewise Structural Equation Models (SEM) of reef fish alpha stability
Path diagrams are illustrated for a marine protected areas (MPA) and b open areas (OA). Positive (negative) links are shown in blue (orange), with path size proportional to the standardized regression coefficient. Not significant paths (p > 0.05) are shown in light grey. Numbers within boxes indicate the variance explained by fixed (marginal, left) and total – i.e. fixed and random together – (conditional, right) effects in the model. c Standardized direct and indirect effect sizes (means and 95% Confidence Intervals derived from n = 10,000 bootstrap replicates of the SEM model) of factors influencing alpha and species stability and species asynchrony in MPA (blue) and OA (orange). Effect sizes whose confidence intervals do not overlap with zero (dashed red line) are considered significant. Positive (negative) effect sizes indicate larger (lower) stability or asynchrony in MPAs than open areas. ASYNC: species asynchrony; SP.STAB: species stability; FRIC: functional richness; MHW: marine heatwaves intensity; REM: remoteness. The not significant (p > 0.5) link from remoteness to functional richness was removed from the original MPA path diagram to improve model fit (Fisher’s C statistic: p > 0.05 for both models).
Thermal sensitivity trends of reef fish
Panels show the trajectories obtained by fitting Generalized Additive Mixed Models (GAMMs) to the abundance (log-transformed and standardized) of four fish trophic categories with thermal affinities below (thermally sensitive species) or equal-above (thermally resistant species) the thermal threshold, against mean intensity of marine heatwaves (MHWs). Thermal thresholds are based on the maximum MHW intensity recorded at a site during the sampling period. Trends are plotted separately for marine protected areas (MPA, blue lines, and symbols) and open areas (OA, orange lines, and symbols); filled areas indicate standard errors; data are shown as z-scores. Panels include GAMM effective degrees of freedom, their significance (***p < 0.001; **p < 0.01; *p < 0.05) and the coefficients of determination (R²). Full statistical results are reported in Supplementary Table 4.
Stability of marine protected area (MPA) networks
a Ecoregions used in the analysis of stability and asynchrony at the metacommunity level. There were at least two MPA and two open area sites in each ecoregion (see Supplementary Table 5 for details). Panels b–e show the posterior distributions of effect sizes comparing different stability measures between MPAs and open areas in relation to the spatial scale of the MPA network (see also Fig. 1). See Supplementary Fig. 12 for asynchrony. Distributions are shown with 66% (thick bar) and 95% (thin bar) uncertainty intervals (n = 12,000 posterior samples). Intervals that do not overlap with 0 (dashed red line) are considered significant. Positive (negative) effect sizes indicate larger (lower) stability in MPAs than in open areas.
Marine protected areas promote stability of reef fish communities under climate warming

February 2024

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711 Reads

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8 Citations

Protection from direct human impacts can safeguard marine life, yet ocean warming crosses marine protected area boundaries. Here, we test whether protection offers resilience to marine heatwaves from local to network scales. We examine 71,269 timeseries of population abundances for 2269 reef fish species surveyed in 357 protected versus 747 open sites worldwide. We quantify the stability of reef fish abundance from populations to metacommunities, considering responses of species and functional diversity including thermal affinity of different trophic groups. Overall, protection mitigates adverse effects of marine heatwaves on fish abundance, community stability, asynchronous fluctuations and functional richness. We find that local stability is positively related to distance from centers of high human density only in protected areas. We provide evidence that networks of protected areas have persistent reef fish communities in warming oceans by maintaining large populations and promoting stability at different levels of biological organization.


A diverse portfolio of marine protected areas can better advance global conservation and equity

February 2024

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327 Reads

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10 Citations

Proceedings of the National Academy of Sciences

Marine protected areas (MPAs) are widely used for ocean conservation, yet the relative impacts of various types of MPAs are poorly understood. We estimated impacts on fish biomass from no-take and multiple-use (fished) MPAs, employing a rigorous matched counterfactual design with a global dataset of >14,000 surveys in and around 216 MPAs. Both no-take and multiple-use MPAs generated positive conservation outcomes relative to no protection (58.2% and 12.6% fish biomass increases, respectively), with smaller estimated differences between the two MPA types when controlling for additional confounding factors (8.3% increase). Relative performance depended on context and management: no-take MPAs performed better in areas of high human pressure but similar to multiple-use in remote locations. Multiple-use MPA performance was low in high-pressure areas but improved significantly with better management, producing similar outcomes to no-take MPAs when adequately staffed and appropriate use regulations were applied. For priority conservation areas where no-take restrictions are not possible or ethical, our findings show that a portfolio of well-designed and well-managed multiple-use MPAs represents a viable and potentially equitable pathway to advance local and global conservation.


From local seafloor imagery to global patterns in benthic habitat states: contribution of citizen science to habitat classification across latitudes

February 2024

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97 Reads

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1 Citation

Aim The aim of this study was to define reef benthic habitat states and explore their spatial and temporal variability at a global scale using an innovative clustering pipeline. Location The study uses data on the transects surveyed on shallow (< 20m) reef ecosystems across the globe. Time period: Transects sampled between 2008 and 2021. Major taxa studied: Macroalgae, sessile invertebrates, hydrozoans, seagrass, corals. Methods Percentage cover was estimated for 24 functional groups of sessile biota and substratum from annotated underwater photoquadrats taken along 6,554 transects by scuba divers contributing to the Reef Life Survey dataset. A clustering pipeline combining a non-linear dimension-reduction technique ( UMAP ), with a density-based clustering approach ( HDBSCAN ), was used to identify benthic habitat states. Spatial and temporal variation in habitat distribution was then explored across ecoregions. Results The UMAP-HDBSCAN pipeline identified 17 distinct clusters representing different benthic habitats and gradients of ecological state. Certain habitat states displayed clear biogeographic patterns, predominantly occurring in temperate regions or tropical waters. Notably, some reefs dominated by turf algae were ubiquitous across latitudinal zones. Transition zones between temperate and tropical waters emerged as spatial hotspots of habitat state diversity. Temporal analyses revealed changes in the proportion of certain states over time, notably an increase in turf algae occurrence. Main Conclusions The UMAP-HDBSCAN clustering pipeline effectively characterised fine-scale benthic habitat states at a global scale, confirming known broader biogeographic patterns, including the importance of temperate-tropical transition zones as hotspots of habitat state diversity. This fine-scale, yet broadly-scalable habitat classification could be applied as a standardised template for tracking benthic habitat change across space and time at a global scale. The UMAP-HDBSCAN pipeline has proven to be a powerful and versatile approach for analysing complex biological datasets and can be applied in various ecological domains.


Citations (75)


... Based on a new methodology of catch time series in support of fisheries management [18], a scientific review of the evidence [19] suggests that the regeneration capacity of overexploited stocks is prone to over-optimistic projections. This is based on a reanalysis of publicly available data of 230 well-known exploited fish species. ...

Reference:

When Mediterranean Artisanal Fishers Protect Coastal Ecosystems
Stock assessment models overstate sustainability of the world's fisheries
  • Citing Article
  • August 2024

Science

... richness since different species react differently to human vs. protection effects (Sanchez et al. 2024) so, on the balance, species richness is either similar inside and outside protected areas or sometimes even more important outside than inside (Boulanger et al. 2021). As shown by Sanabria-Fernandez et al. (2019), MPAs efficiency may vary within regions meaning that some of them can be ineffective so compliance measures are necessary. ...

Rarity mediates species‐specific responses of tropical reef fishes to protection

Ecology Letters

... Marine protected areas play a crucial role in safeguarding species and their habitats from the anthropogenic pressures (e.g. overexploitation, disturbance, habitat destruction, and pollution) (Benedetti-Cecchi et al., 2024;S. S. Haque et al., 2023). ...

Marine protected areas promote stability of reef fish communities under climate warming

... We therefore chose the approach of using models at large spatial scales to define our available species pool, and the country-level Sea Around Us data to define our fished species pool. Species distribution and biomass models would further benefit from the inclusion of local-scale environmental variables, for example, using local benthic and pelagic habitat variables such as coral and algae cover, water turbidity, wave exposure and terrestrial run-off (Lyons et al., 2024;Violet et al., 2024). While we did not aim to model intra-country variation in species presence and biomass, doing so is an important future step that could provide a more accurate comparison between fisheries catch and source pools at smaller spatial scales. ...

From local seafloor imagery to global patterns in benthic habitat states: contribution of citizen science to habitat classification across latitudes

... However, anthropogenic activities in recent decades have dramatically impacted biodiversity and ecosystem health and reduced the capacity of these systems to provide such services [3]. In response, Marine Protected Areas (MPAs), have been increasingly advocated as a means to improve the spatial and temporal allocation of human activities, and mitigate their impact in the marine environment [4]. If managed effectively, MPAs have the potential to restore population size and diversity within their boundaries and support neighbouring fisheries through spill-over and larval export (e.g. ...

A diverse portfolio of marine protected areas can better advance global conservation and equity

Proceedings of the National Academy of Sciences

... We apply the TSR as a reduction of 5%°C −1 in consumer size thresholds including the length l v below which juveniles are vulnerable to predation, maturation length l mat , and/or asymptotic length l ∞ (Figure 1b, Equation 10b), based on the estimated mass-specific mean reduction under warming for aquatic ectotherms (Coghlan et al. 2024;Forster, Hirst, and Atkinson 2012) and length-weight allometry of w ∼ l 3 (Text S1). While TSR applied to l mat and/or l ∞ mimics reduction in consumer size with warming, TSR applied to predation size threshold l v mimics reduction in predator size with warming. ...

Mean reef fish body size decreases towards warmer waters

Ecology Letters

... In complex models such as the ones presented here with many interacting species it is very difficult to provide a comprehensive description of all the dynamics occurring, requiring more sophisticated statistical approaches. Audzijonyte et al. (2023) use a statistical model to help to understand ecosystem responses and interactions across levels of organisation and experimental treatments. Reum et al. (2024) show these population dynamics propagate from individual to community levels, and depend on both food web structure and temperature dependence. ...

Changes in sea floor productivity are crucial to understanding the impact of climate change in temperate coastal ecosystems according to a new size-based model

... Therefore, biomass recovery data and associated confidence intervals of r sets a wide interval for the estimated total community surplus production. The average production might be accurate if all taxa contributed proportionally or if losses of production were compensated for by resistant taxa across the fishing effort sequence [38][39][40]. Life history variability is expected to be large and influential enough in species diverse ecosystems to deviate production significantly from community level predictions. ...

Sustainable reference points for multispecies coral reef fisheries

... This is becoming increasingly important as reef ecosystems are rapidly changing (Vergés et al. 2014;Filbee-Dexter and Wernberg 2018;Tebbett et al. 2023). In this respect, the restructuring of fish communities along latitudinal gradients in response to warming represents a marked change on reef systems globally (Stuart-Smith et al. 2022;Nagelkerken et al. 2023). ...

The effects of climate change on the ecology of fishes

... In this study, a comprehensive structural equation modelling (SEM) approach provided a unique perspective on the organisation of the coral reef food web in an oceanic atoll system. Unlike traditional linear modelling techniques, this approach allows for a thorough exploration of the often indirect relationships in the food web, yet to date, they have been infrequently used in marine systems (but see Casey et al. 2017;Morais and Bellwood 2019;Desbiens et al. 2021;Brown et al. 2023). The final SEM revealed significant connections among predators, their prey, and the habitat, demonstrating that energy flows from the base of the food web to upper trophic levels through their prey. ...

Entry fees enhance marine protected area management and outcomes

Biological Conservation