Hamish A. Malcolm’s research while affiliated with New South Wales Department of Primary Industries and other places

What is this page?


This page lists works of an author who doesn't have a ResearchGate profile or hasn't added the works to their profile yet. It is automatically generated from public (personal) data to further our legitimate goal of comprehensive and accurate scientific recordkeeping. If you are this author and want this page removed, please let us know.

Publications (62)


Genomic analyses indicate resilience of a commercially and culturally important marine gastropod snail to climate change
  • Article
  • Full-text available

November 2023

·

98 Reads

·

·

·

[...]

·

Genomic vulnerability analyses are being increasingly used to assess the adaptability of species to climate change and provide an opportunity for proactive management of harvested marine species in changing oceans. Southeastern Australia is a climate change hotspot where many marine species are shifting poleward. The turban snail, Turbo militaris is a commercially and culturally harvested marine gastropod snail from eastern Australia. The species has exhibited a climate-driven poleward range shift over the last two decades presenting an ongoing challenge for sustainable fisheries management. We investigate the impact of future climate change on T. militaris using genotype-by-sequencing to project patterns of gene flow and local adaptation across its range under climate change scenarios. A single admixed, and potentially panmictic, demographic unit was revealed with no evidence of genetic subdivision across the species range. Significant genotype associations with heterogeneous habitat features were observed, including associations with sea surface temperature, ocean currents, and nutrients, indicating possible adaptive genetic differentiation. These findings suggest that standing genetic variation may be available for selection to counter future environmental change, assisted by widespread gene flow, high fecundity and short generation time in this species. We discuss the findings of this study in the content of future fisheries management and conservation.

Download

Extended and spatially asynchronous reproductive periodicity in a harvested, warm-temperate rocky-reef gastropod (Turbinidae)

September 2023

·

101 Reads

·

1 Citation

Fisheries Oceanography

Turban snails are targeted for their high-quality meat and, consequently, are often subjected to heavy harvesting pressure. Managing recreational and small-scale fisheries is challenging, partly due to a lack of biological data underpinning certain regulatory measures. This study aimed to fill current knowledge gaps on the reproductive cycle of the recreationally and culturally harvested Australian turbinid, Turbo militaris. The objectives were to investigate the reproductive timing of T. militaris in New South Wales (NSW) and identify likely environmental drivers of reproductive period-icity. Oocytes and gonads were sampled from wild animals monthly over 15 months at two sites separated by $500 km. Analysis of oocyte size frequency and gonadoso-matic index revealed that T. militaris has a pattern of extended reproduction, which is synchronous between sexes. Turbo militaris was ripest during summer, and spawning appears to have occurred over multiple events, although primarily during winter. Reproductive timing was associated with environmental explanatory variables, including sea surface temperature, wave height, salinity, phytoplankton and nitrate concentration, together accounting for 81% of the variation in oocyte size frequency and 67% in the gonadosomatic index. Reproductive periodicity was correlated with wave conditions and phytoplankton concentrations inconsistently between sites, indicating that the effect of some environmental conditions may be unpredictable or site-specific. Reproductive timing was asynchronous between two sites in the NSW fishery, posing challenges for designing seasonal fishing closures and community-based harvesting rules. Spatial closures for species with spawning over extended timeframes, or spatially asynchronous reproductive cycles, are potentially more suitable for achieving fisheries management objectives.


Using repeated annual surveys of tagged individual colonies, conducted between 2016 and 2019, we quantified the influence of environmental stochasticity on the long‐term performance and short‐term potential of tropical and subtropical coral populations in southern Japan and eastern Australia. (A) As climate shifts induce range expansions in many coral species worldwide, their populations are increasingly exposed to a gradient in thermal regimes, illustrated here by mean monthly sea surface temperatures (x̄sst; degree Celsius; sst, sea surface temperature) recorded between 1950 and 2019 (Rayner et al., 2003). (B) Between 2016 and 2019, we documented the survival, growth, fragmentation, and recruitment patterns of 3171 tagged coral individuals within the tropical reef communities (▲) of Okinawa (Japan) and Heron Island (Australia), and within the subtropical communities (●) of Kochi (Japan) and the Solitary Islands Marine Park (Australia). (C) Using these data, we parameterized integral projection models (IPMs) describing the dynamics of tropical and subtropical assemblages of competitive, stress‐tolerant, and weedy coral taxa. Combining outputs obtained from these models with measures of the thermal regimes experienced by each population, we then explored the relationships between the long‐term performance and short‐term potential of coral populations, and their exposure to gradients in abiotic variability.
Contrasting patterns in long‐term performance and short‐term potential across our examined coral populations, corresponding with their relative exposure to abiotic variability. Partial least squares regression score plot illustrating the association between measures of abiotic variability, and the long‐term performance (λ) and short‐term potential (transient envelope [TE] and damping ratio [ρ]) of tropical (▲) and subtropical (●) populations of competitive (blue), stress‐tolerant (yellow), and weedy (red) coral taxa. We quantified the abiotic variability experienced by each coral population using representative measures of local sea surface temperature (SST) regimes (McIlroy et al., 2019; Toth et al., 2021). Specifically, we used SSTs recorded between 1950 and 2019 to calculate regional estimates of mean monthly SST (x̄sst), monthly SST variance (cvsst), and monthly SST frequency spectrum (βsst). Component scores illustrate the relative degree of variance explained in the abiotic predictor variables, whereas ry2 reflects the cumulative variance explained across the demographic characteristics. The shaded polygons reflect the clustering of tropical and subtropical populations, whereas the dotted lines delineate regions of association to facilitate the visualization of patterns in correlation between the abiotic and demographic variables.
Inter‐specific variation within the contrasting patterns observed between long‐term performance and short‐term potential across tropical and subtropical coral assemblages correlates with patterns in population turnover rate. (A) Interaction plot showcasing how estimates of demographic stability index (DSI) vary between associated tropical (▲) and subtropical (●) assemblages of competitive (blue), stress‐tolerant (yellow), and weedy (red) coral taxa in Australia and Japan. We present DSI, as an inverse measure of maximal amplification (ρ¯max), describing the ability for populations to undergo elevated growth following disturbance. Thus, lower DSI estimates correspond with a greater capacity for demographic amplification. We also applied Type 2 linear regression to separately explore the association of population turnover characteristics with (B) long‐term performance (asymptotic population growth rate; λ), and (C) short‐term potential (transient envelope, TE) across tropical and subtropical populations of competitive, stress‐tolerant, and weedy coral taxa in Australia and Japan. We note here that TE estimates were reversed during transformation to achieve normality, thus higher values reflect diminished short‐term potential. We have therefore displayed short‐term potential on a reversed scale to facilitate comparisons with patterns in long‐term performance (λ). We used generation time (years; displayed here on the log scale) as a measure of population turnover rate, with higher estimates reflecting slower rates of population turnover. Across panels (B) and (C), r² values are provided as a measure of model fit. Across all panels error is displayed using 95% confidence intervals.
Coral assemblages at higher latitudes favor short‐term potential over long‐term performance

July 2023

·

241 Reads

·

5 Citations

The persistent exposure of coral assemblages to more variable abiotic regimes is assumed to augment their resilience to future climatic variability. Yet, while the determinants of coral population resilience across species remain unknown, we are unable to predict the winners and losers across reef ecosystems exposed to increasingly variable conditions. Using annual surveys of 3171 coral individuals across Australia and Japan (2016–2019), we explore spatial variation across the short‐ and long‐term dynamics of competitive, stress‐tolerant, and weedy assemblages to evaluate how abiotic variability mediates the structural composition of coral assemblages. We illustrate how, by promoting short‐term potential over long‐term performance, coral assemblages can reduce their vulnerability to stochastic environments. However, compared to stress‐tolerant, and weedy assemblages, competitive coral taxa display a reduced capacity for elevating their short‐term potential. Accordingly, future climatic shifts threaten the structural complexity of coral assemblages in variable environments, emulating the degradation expected across global tropical reefs.


Habitat limits the poleward establishment of anemonefishes in a climate change hotspot

November 2021

·

28 Reads

·

6 Citations

Estuarine Coastal and Shelf Science

Climate change is modifying marine species' distribution with consequences for the structure and function of ecosystems. The warming and strengthening East Australian Current (EAC) is driving the tropicalisation of subtropical marine ecosystems through changing overwinter survival of tropical species. However, this can be complex for obligate symbionts, such as anemonefishes. Here, we documented fine-scale temporal changes in the density of anemonefishes and assessed the influence of latitude, temperature, and the availability of host sea anemones. Juvenile, subadult and adult Amphiprion akindynos and A. latezonatus occurred at all study locations: North Solitary Island (equatorward), South Solitary Island, and Fish Rock (poleward). While the sea anemone Heteractis crispa was readily available at Fish Rock, we found that a lack of another sea anemone Entacmaea quadricolor hindered the establishment of adult A. akindynos and A. latezonatus populations. Minimum water temperature was also a bottleneck for the tropical anemonefish A. akindynos, but not for the subtropical A. latezonatus. Our findings suggest anemonefishes are capable of contributing to the tropicalisation of the east coast of Australia. However, poleward establishment is currently limited by the absence of the preferred host sea anemone.


Figure 1
Figure 2
Coral assemblages at higher latitudes favour short-term potential over long-term performance

October 2021

·

282 Reads

·

2 Citations

The current exposure of species assemblages to high environmental variability may grant them resilience to future increases in climatic variability. In globally threatened coral reef ecosystems, management seeks to protect resilient reefs within variable environments. Yet, our lack of understanding for the determinants of coral population performance within variable environments hinders forecasting the future reassembly of coral communities. Here, using Integral Projection Models, we compare the short- ( i.e. , transient) and long-term ( i.e. , asymptotic) demographic characteristics of tropical and subtropical coral assemblages to evaluate how thermal variability influences the structural composition of coral communities over time. Exploring spatial variation across the dynamics of functionally different competitive, stress-tolerant, and weedy coral assemblages in Australia and Japan, we show that coral assemblages trade-off long-term performance for transient potential in response to thermal variability. We illustrate how coral assemblages can reduce their susceptibility towards environmental variation by exploiting volatile short-term demographic strategies, thus enhancing their persistence within variable environments. However, we also reveal considerable variation across the vulnerability of competitive, stress-tolerant, and weedy coral assemblages towards future increases in thermal variability. In particular, stress-tolerant and weedy corals possess an enhanced capacity for elevating their transient potential in response to environmental variability. Accordingly, despite their current exposure to high thermal variability, future climatic shifts threaten the structural complexity of coral assemblages, derived mostly from competitive coral taxa within highly variable subtropical environments, emulating the degradation expected across global coral communities.


Locations of baited remote underwater stereo‐video (stereo‐BRUV) deployments (i.e., samples, n = 2904) across Australian neritic (1–50 m) continental shelf systems (green, samples in no‐take marine reserves [NTMRs] boundaries, n = 541; red, samples outside NTMR boundaries, n = 2363; light blue, temperate waters; orange, tropical waters)
Drivers and patterns of fished species occurrence and abundance across Australian neritic (1–50 m) continental shelf systems: (a) relative importance of explanatory variables to predict the probability of occurrence of large fishes (>90th percentile of body size distribution) and abundance of legal (≥ minimum legal size [MLS]) and sublegal (<MLS) fishes, (b–k) best generalized additive mixed models for predicting the probability of occurrence of (b–d) large fishes and abundance of (e–h) legal and (i–k) sublegal fishes (MaxN, maximum number of individuals at one time; solid lines, mean fitted values from cubic regression splines with other predictors in the top‐ranked models held constant; gray bands, 95% CI [including random effect variances]; SST, sea surface temperature (° C); NPP, net primary productivity [mg C/m² day])
Size‐specific determinants of fished species occurrence and abundance across Australian neritic (1–50 m) continental shelf systems: relative importance (pooled Akaike weights [ωAIC ]) of (a) anthropogenic (human gravity [i.e., a proxy of human impacts] and management status), (b) environmental (nitrate, net primary productivity [NPP] mean, NPP standard deviation [NPP SD], sea surface temperature [SST] mean, and SST standard deviation [SST SD]), and (c) habitat (relief and depth) covariates to predict the probability of occurrence of large (>90th percentile of body size distribution) fishes and the abundance of legal (≥minimum legal size [MLS]) and sublegal (<MLS) fishes
Model‐averaged coefficients (SE) from generalized linear mixed models testing the effect of (a) human gravity (i.e., a proxy of human impacts) and (b) no‐take marine reserves (NTMRs) on the probability of occurrence of large fishes (dark squares), and the abundance of legal (gray triangles) and sublegal (light gray circles) fishes. Coefficients depict the magnitude of the effect while controlling for other environmental and habitat predictors and accounting for uncertainty of the models
Effects of human footprint and biophysical factors on the body‐size structure of fished marine species

July 2021

·

328 Reads

·

25 Citations

Marine fisheries in coastal ecosystems in many areas of the world have historically removed large‐bodied individuals, potentially impairing ecosystem functioning and the long‐term sustainability of fish populations. Reporting on size‐based indicators that link to food‐web structure can contribute to ecosystem‐based management, but the application of these indicators over large (cross‐ecosystem) geographical scales has been limited to either fisheries‐dependent catch data or diver‐based methods restricted to shallow waters (<20 m) that can misrepresent the abundance of large‐bodied fished species. We obtained data on the body‐size structure of 82 recreationally or commercially targeted marine demersal teleosts from 2904 deployments of baited remote underwater stereo‐video (stereo‐BRUV). Sampling was at up to 50 m depth and covered approximately 10,000 km of the continental shelf of Australia. Seascape relief, water depth, and human gravity (i.e., a proxy of human impacts) were the strongest predictors of the probability of occurrence of large fishes and the abundance of fishes above the minimum legal size of capture. No‐take marine reserves had a positive effect on the abundance of fishes above legal size, although the effect varied across species groups. In contrast, sublegal fishes were best predicted by gradients in sea surface temperature (mean and variance). In areas of low human impact, large fishes were about three times more likely to be encountered and fishes of legal size were approximately five times more abundant. For conspicuous species groups with contrasting habitat, environmental, and biogeographic affinities, abundance of legal‐size fishes typically declined as human impact increased. Our large‐scale quantitative analyses highlight the combined importance of seascape complexity, regions with low human footprint, and no‐take marine reserves in protecting large‐bodied fishes across a broad range of species and ecosystem configurations.


Map showing the Solitary Islands Marine Park, New South Wales, eastern Australia. Insets mark the sampling sites on the western side of the islands with the approximate location of transects (T1–T3) and temperature loggers (black crosses). Offshore islands: North Solitary Island, South Solitary Island; Mid-shelf islands: Northwest Solitary Island, Southwest Solitary Island
In situ seawater temperature trends for the Solitary Islands at 10 m depth. Each plot shows the same average DHW1C temperature anomaly threshold (flat dotted brown line), and the same 2001–2009 baseline temperature trend (mean ± 95% CI, dark grey line and ribbon) derived from daily baseline site temperatures (pale grey points). For each subsequent year (individual plots), mean daily temperatures across sites (red lines) are shown relative to the baseline and as among-site average DHW1C (blue lines). Average trends were shown due to high consistency among sites. Summative bleaching status from surveys/observations are also noted on each plot as Severe or None for years with survey data, and as Not Reported or Anecdotal (Malcolm personal comms) for years without survey data
Size-frequency distributions of log-transformed colony area for Pocillopora aliciae populations at offshore (red shading: North Solitary Island and South Solitary Island) and mid-shelf (blue shading: Northwest Solitary Island and Southwest Solitary Island) islands in austral spring, and during coral bleaching (2016a). The dashed line represents the juvenile–adult cut-off size. Histograms and probability densities were computed using 10 equal colony area bins. Common letters identify groups of years within which size-frequency distributions do not differ significantly based on site-specific GLMMs and Tukey tests (Table S1)
Temporal trends in coral density for a all Pocillopora aliciae corals, b juveniles only and c adults only from offshore (red shading) and mid-shelf (blue shading) regions, showing mean ± 95% CI. Common letters identify groups of years within which coral densities are not significantly different based on GLMMs and Tukey tests for offshore and mid-shelf areas independently (Table S2). Dashed arrows indicate significant consecutive temporal transitions. Points represent raw photo count data. Site-level means ± 95% CI are shown in Fig. S6
Effects of maximum juvenile thermal stress (DHW1C-max) on: a juvenile coral density and b adult coral density based on GLMMs, for offshore (red shading) and mid-shelf (blue shading) regions. Fitted values (line ± 95% bootstrapped CI) are based on photo-level counts, while points show transect-level mean coral density ± 95% CI and site-level DHW1C-max values
Linking population size structure, heat stress and bleaching responses in a subtropical endemic coral

June 2021

·

381 Reads

·

24 Citations

Coral Reefs

Anthropocene coral reefs are faced with increasingly severe marine heatwaves and mass coral bleaching mortality events. The ensuing demographic changes to coral assemblages can have long-term impacts on reef community organisation. Thus, understanding the dynamics of subtropical scleractinian coral populations is essential to predict their recovery or extinction post-disturbance. Here we present a 10-yr demographic assessment of a subtropical endemic coral, Pocillopora aliciae (Schmidt-Roach et al. in Zootaxa 3626:576–582, 2013) from the Solitary Islands Marine Park, eastern Australia, paired with long-term temperature records. These coral populations are regularly affected by storms, undergo seasonal thermal variability, and are increasingly impacted by severe marine heatwaves. We examined the demographic processes governing the persistence of these populations using inference from size-frequency distributions based on log-transformed planar area measurements of 7196 coral colonies. Specifically, the size-frequency distribution mean, coefficient of variation, skewness, kurtosis, and coral density were applied to describe population dynamics. Generalised Linear Mixed Effects Models were used to determine temporal trends and test demographic responses to heat stress. Temporal variation in size-frequency distributions revealed various population processes, from recruitment pulses and cohort growth, to bleaching impacts and temperature dependencies. Sporadic recruitment pulses likely support population persistence, illustrated in 2010 by strong positively skewed size-frequency distributions and the highest density of juvenile corals measured during the study. Increasing mean colony size over the following 6 yr indicates further cohort growth of these recruits. Severe heat stress in 2016 resulted in mass bleaching mortality and a 51% decline in coral density. Moderate heat stress in the following years was associated with suppressed P. aliciae recruitment and a lack of early recovery, marked by an exponential decrease of juvenile density (i.e. recruitment) with increasing heat stress. Here, population reliance on sporadic recruitment and susceptibility to heat stress underpin the vulnerability of subtropical coral assemblages to climate change.


Increased connectivity and depth improve the effectiveness of marine reserves

May 2021

·

417 Reads

·

43 Citations

Global Change Biology

Marine reserves are a key tool for the conservation of marine biodiversity, yet only ~2.5% of the world's oceans are protected. The integration of marine reserves into connected networks representing all habitats has been encouraged by international agreements, yet the benefits of this design has not been tested empirically. Australia has one of the largest systems of marine reserves, providing a rare opportunity to assess how connectivity influences conservation success. An Australia-wide dataset was collected using baited remote underwater video systems deployed across a depth range from 0 to 100 m to assess the effectiveness of marine reserves for protecting teleosts subject to commercial and recreational fishing. A meta-analytical comparison of 73 fished species within 91 marine reserves found that, on average, marine reserves had 28% greater abundance and 53% greater biomass of fished species compared to adjacent areas open to fishing. However, benefits of protection were not observed across all reserves (heterogeneity), so full subsets generalized additive modelling was used to consider factors that influence marine reserve effectiveness, including distance-based and ecological metrics of connectivity among reserves. Our results suggest that increased connectivity and depth improve the aforementioned marine reserve benefits and that these factors should be considered to optimize such benefits over time. We provide important guidance on factors to consider when implementing marine reserves for the purpose of increasing the abundance and size of fished species, given the expected increase in coverage globally. We show that marine reserves that are highly protected (no-take) and designed to optimize connectivity, size and depth range can provide an effective conservation strategy for fished species in temperate and tropical waters within an overarching marine biodiversity conservation framework.


The BRUVs workshop -An Australia-wide synthesis of baited remote underwater video data to answer broad-scale ecological questions about fish, sharks and rays

May 2021

·

534 Reads

·

28 Citations

Marine Policy

Many marine fish populations have declined due to the individual or cumulative impacts of increasing water temperatures, ocean acidification, overfishing and other human-induced impacts such as land run-off, dredging and habitat alteration. Some solutions may be offered by ecosystem-based fisheries and conservation management. However, understanding their effectiveness relies on the availability of good quality data on the size distributions and abundance of fish populations and assemblages, collected at appropriate temporal and spatial scales. Since the early 2000s, baited remote underwater video systems (BRUVs) have become a popular tool for collecting data on fish assemblages across a range of depths and habitats. In Australia, this technique has been adopted by many different agencies and institutions, creating a unique opportunity to compile a continental-scale synthesis of fish data using a standardised sampling technique. Key Australian researchers and managers were invited to contribute to a synthesis workshop on baited underwater video in Albany, Western Australia between the 4th and 8th of February 2018. Data from 19,939 BRUVs deployments, collected between 2000 and 2017 around Australia, were compiled using GlobalArchive (globalarchive.org). The workshop identified and prioritised several key research themes that would contribute to the conservation and sustainable management of focal species and broad assemblages. Our goal is to describe where and when the data were collected, the type of equipment used and how the imagery was analysed. We also discuss the types of questions that can be addressed by analysing these standardised datasets and the potential benefits to conservation and fisheries management.


A coherent, representative, and bioregional marine reserve network shows consistent change in rocky reef fish assemblages

April 2021

·

254 Reads

·

27 Citations

Worldwide, several countries have established coherent, representative, and large-scale networks of marine reserves to conserve biodiversity. Very few have, however, published systematic assessments of the ecological responses to this network protection, hindering broad understanding of their generality, utility, and efficacy. We present data collected from systematic sampling of rocky reef fish assemblages at sites across a network of 27 no-take marine reserve areas (NTMR) and 27 partially protected areas (PPA) nested within multiple marine parks (regional networks) across three Australian bioregions spanning >1000 km of coastline (7° latitude) to test the generality of ecological change across this network. We also sampled 18 reference areas (outside of the marine parks) to provide an independent assessment of potential NTMR effects and also to assess whole marine park effects. Baited remote underwater video (BRUV) was used to sample fishes between depths of 20–40 m over austral winters in four years (2010, 2011, 2015, and 2016). Despite substantial bioregional differences in fish assemblages, large and consistent effects of NTMR protection were detected across all bioregions for a key commercially and recreationally harvested species, Chrysophrys auratus (pink snapper). There were substantial increases in relative abundance of C. auratus in NTMR compared with fished zones through time (effect sizes >150%). The wider assemblage of targeted fish (excluding C. auratus) only showed relatively small effects of protection (~11%) with trends observed for site-attached wrasses (labrids) and planktivores (e.g., commercially fished Scorpis lineolata) that are recreationally and commercially harvested. Furthermore, the relative abundance of non-target or by-catch species generally did not differ among management zones across the bioregional network. These results highlight how NTMR can be used to assess the ecological effects of fishing and wider environmental management, and can be incorporated into ecosystem-based management for reef species more generally. Importantly, the provision of robust evidence of the performance and generality of NTMR over large-spatial scales (e.g., bioregions) provides greater confidence in the expected outcomes from marine reserve networks as a conservation management approach.


Citations (53)


... While there have been extensive investigations of the population dynamics of corals and fishes in the east Australian transition zone with respect to regional warming (Cant et al., , 2023Lachs et al., 2021;Malcolm et al., 2010;Sommer et al., 2014Sommer et al., , 2018Vergés et al., 2016), less is known about sea urchins and other benthic species. The subtropical reefs around the SIMP have high diversity of sea urchins, with 26 species recorded to date (Shaw, 2023), including tropical (e.g. ...

Reference:

Taxa‐dependent temporal trends in the abundance and size of sea urchins in subtropical eastern Australia
Coral assemblages at higher latitudes favor short‐term potential over long‐term performance

... The ecological objectives of habitat mapping are wide ranging and include characterizing baseline conditions (Smith et al. 2015;Oakley et al. 2012;Hewitt et al. 2004), investigating the relationship between biological species/communities and environmental parameters across various spatial scales (Lecours et al. 2015;De Leo et al. 2014;LaFrance et al. 2014;McArthur et al. 2010;Ierodiaconou et al. 2007;Zajac et al. 2000), and creating species or habitat prediction and modeling tools (Porskamp et al. 2018;Ierodiaconou et al. 2018Ierodiaconou et al. , 2011Lecours et al. 2017;Mitchell et al. 2017;Young et al. 2015;Valesini et al. 2010;Degraer et al. 2008). In addition to studying an area of interest, mapping efforts can focus on a specific habitat type, such as fish habitat (Malcolm et al. 2016;Kendall et al. Communicated by Brian B. Barnes 2011;Rooper and Zimmermann 2007;Friedlander et al. 2006) or habitats that exhibit unique acoustic signatures and can be readily identified in sidescan sonar imagery, including submerged aquatic vegetation (e.g., Greene et al. 2018;Sánchez-Carnero et al. 2012;Lefebvre et al. 2009;Jones et al. 2007;Sabol et al. 2002), shellfish beds (e.g., Isachenko et al. 2014;Raineault et al. 2012;van Overmeeren et al. 2009;Kostylev et al. 2003), coral reefs (e.g., El-Gharabawy et al. 2017;Collier and Humber 2007;Kendall et al. 2005;Roberts et al. 2005;Mumby et al. 2004), and artificial reefs (e.g., Dong et al. 2017;Raineault et al. 2013). ...

Integrating Seafloor Habitat Mapping and Fish Assemblage Patterns Improves Spatial Management Planning in a Marine Park
  • Citing Article
  • March 2016

Journal of Coastal Research

... We hypothesize that the positive S. L. Ziegler et al. other environmental drivers may be more apparent (González-Moreno et al. 2015). For instance, the lack of suitable habitat (host anemones) is limiting the establishment of tropical anemonefish populations in more temperate locations along the coast of eastern Australia regardless of temperature differences from its native range (Pryor et al. 2022). ...

Habitat limits the poleward establishment of anemonefishes in a climate change hotspot
  • Citing Article
  • November 2021

Estuarine Coastal and Shelf Science

... remedying data biases was beyond the scope of this study, we must also acknowledge geographic and taxonomic biases implicit within our sources of demographic data (see Paniw et al., 2021;Römer et al., 2021;Salguero-Gómez et al., 2021; Figure 1a). Environmental stochasticity plays a crucial role in regulating species range boundaries (Benning et al., 2022;Feldman et al., 2015), and indeed, the transient dynamics of coral assemblages in southern Japan and eastern Australia mediate their capacity for persisting outside of their core ranges (Cant et al., 2021;Cant, Cook, et al., 2022). Yet coral populations represent a taxonomic group for which there is not yet extensive demographic data available (Edmunds & Riegl, 2020). ...

Coral assemblages at higher latitudes favour short-term potential over long-term performance

... To assess the effect of zone, site (Punta Lobos, Los Islotes, and El Bajo), season (warm and cold), year (2021 and 2022), and the interaction between them, a model-based analysis for multivariate abundance data was performed (Wang et al. 2012;Bosch et al. 2021). This method offers advantages over traditional distance-based analyses (e.g., PERMANOVA) as it involves creating generalized linear models (GLMs) per species to make multivariate inferences that are unlikely to fail to meet the assumptions of correlation analysis (Wang et al. 2012). ...

Effects of human footprint and biophysical factors on the body‐size structure of fished marine species

... In contrast, the values for FOri (< 0.25) indicate low redundancy, meaning that a small proportion of species can substitute their functional equivalents in the case of their loss (Rosenfeld 2002;Mason et al. 2005;Mouillot et al. 2013;Francisco and de la Cueva 2017). Moreover, similar values of functional and phylogenetic diversity may indicate that species with similar traits (measured and unmeasured) are replaced in deeper reefs, possibly related to limited resource competition between shallow and mesophotic assemblages, which ultimately might allow the coexistence of evolutionarily and functionally similar species under future conditions (Bosch et al. 2021;Goetze et al. 2021). These results support our hypothesis of the existence of resemblance in fish phylogenetic and functional diversity between zones. ...

Increased connectivity and depth improve the effectiveness of marine reserves

Global Change Biology

... Image-based sampling platforms such as remotely operated vehicles (ROVs) and baited remote underwater video (BRUVs) provide a means of collecting nonextractive video data on the abundance and sizes of target organisms and the habitats in which they reside across large spatial scales and depth ranges (Knott et al., 2021;Sward et al., 2019). Evidence is beginning to mount that these platforms can be effective tools for detecting the effects of MPAs in mesophotic depths (e.g., Knott et al., 2021;Vigo et al., 2023). ...

A coherent, representative, and bioregional marine reserve network shows consistent change in rocky reef fish assemblages

... Several hypotheses have emerged on the importance of these systems including the capability of coral reefs in subtropical regions to act as refugia for tropical species [22][23][24], and poleward expansion of tropical species [25,26]. Other studies point to the higher risk of endemic species from subtropical systems due to limited connectivity with source populations and thermal susceptibility of species [27,28]. As such, uncertainty remains in predicting survival, diversity, and coverage of subtropical coral species as ocean warming increasingly impacts many of these regions globally. ...

Linking population size structure, heat stress and bleaching responses in a subtropical endemic coral

Coral Reefs

... Furthermore, the underlying processes contributing to species range shifts and homogenisation can have important implications also in terms of the structure and functioning of ecosystems (Beger et al. 2014;Vergés et al. 2019;Maureaud et al. 2020). For instance, in Australian reefs, warming led to an increase in tropical herbivorous fish species and the decline of temperate planktivorous species, which in turn modified the community structure and energy flux (Smith et al. 2021). Therefore, the consideration of both species and traits in diversity studies is key to better understand the underlying processes contributing to community changes (including homogenisation) and their variability in space and time (Bellwood et al. 2002;Swenson, Anglada-Cordero, and Barone 2011;Soininen et al. 2016;Richardson et al. 2018). ...

Tropicalisation and kelp loss shift trophic composition and lead to more winners than losers in fish communities

Global Change Biology

... A diverse array of technologies has been used to deploy cameras for fish quantification including cabled observatories (e.g. Aguzzi et al., 2020), baited remote underwater video systems (BRUVS) (see Harvey et al., 2021 for review), autonomous underwater vehicles (AUVs) (e.g. Seiler et al., 2012), remote operated vehicles (ROVs) (Sward et al., 2019), towed systems (Jones et al., 2009), SCUBA divers (Piazza et al., 2018), drop cameras (Wick et al., 2020) and underwater tripods (Struthers et al., 2015). ...

The BRUVs workshop -An Australia-wide synthesis of baited remote underwater video data to answer broad-scale ecological questions about fish, sharks and rays
  • Citing Article
  • May 2021

Marine Policy