Abstract
A changing climate is driving increasingly common and prolonged marine heatwaves (MHWs) and these extreme events have now been widely documented to severely impact marine ecosystems globally. However, MHWs have rarely been considered when examining temperature-induced degradation of coral reef ecosystems. Here we consider extreme, localized thermal anomalies, nested within broader increases in sea surface temperature, which fulfill the definitive criteria for MHWs. These acute and intense events, referred to here as MHW hotspots, are not always well represented in the current framework used to describe coral bleaching, but do have distinct ecological outcomes, including widespread bleaching, and rapid mass mortality of putatively thermally tolerant coral species. The physical drivers of these localized hotspots are discussed here, and in doing so we present a comprehensive theoretical framework that links the biological responses of the coral photo-endosymbiotic organism to extreme thermal stress and ecological changes on reefs as a consequence of MHW hotspots. We describe how the rapid onset of high temperatures drives immediate heat-stress induced cellular damage, overwhelming mechanisms that would otherwise mitigate the impact of gradually accumulated thermal stress. The warm environment, and increased light penetration of the coral skeleton due to the loss of coral tissues, coupled with coral tissue decay support rapid microbial growth in the skeletal microenvironment, resulting in the widely unrecognized consequence of rapid decay, and degeneration of the coral skeletons. This accelerated degeneration of coral skeletons on a reef scale hinder the recovery of coral populations and increase the likelihood of phase shifts toward algal dominance. We suggest that MHW hotspots, through driving rapid heat-induced mortality, compromise reefs’ structural frameworks to the detriment of long term recovery. We propose that MHW hotspots be considered as a distinct class of thermal stress events in coral reefs, and that the current framework used to describe coral bleaching and mass mortality be expanded to include these. We urge further research into how coral mortality affects bioerosion by coral endoliths.
Coral Bleaching and the Emergence of Marine Heatwaves
It has now been well established that warming oceans compromise the symbiotic relationship that hard corals share with single-celled dinoflagellates known as zooxanthellae (Symbiodiniaceae, Suessiales) (Muscatine and Porter, 1977; LaJeunesse et al., 2018). Normally, the zooxanthellae that reside within corals’ gastrodermal tissue fix carbon through photosynthesis and thereby support the growth and survival of tropical corals (Muscatine and Porter, 1977). The sugars and other organics produced through photosynthesis are translocated to the coral host, meeting its metabolic requirements in the nutrient-poor waters that most corals inhabit (Muscatine and Porter, 1977; Yellowlees et al., 2008). However, when the temperature of the surrounding seawater increases beyond what can be tolerated by the coral host and/or algal symbiont, cellular dysfunction disrupts this symbiosis (). As the partnership breaks down, the coral colony goes white, due to a loss of symbionts and/or a degradation of their pigments which leaves the coral skeleton visible through the now transparent, and symbiont-depleted host tissues (). This phenomenon is therefore known as coral bleaching (Table 1) and generally reduces the survivorship of corals during times of environmental stress (; ).
TABLE 1
| Term | Definition | Source |
| Acclimatization | The behavioral or physiological changes of an organism to increase the endurance of or reduce the source of cellular stress arising from changes in the environment | |
| Antioxidants | A class of enzymes or compounds that scavenge reactive oxygen species (see below) and so prevent cellular oxidative stress. The following are commonly studied in the context of coral bleaching: superoxide dismutase (SOD), glutathione reductase (GR), ascorbate peroxidase (APX), catalase (CAT), and dimethyl sulfoxide (DMSO) | Krueger et al., 2014, 2015; Roberty et al., 2015; |
| Coral bleaching | The disassociation between corals and their colored endosymbiotic algae due to cellular stress, resulting in a characteristic white appearance. Commonly a result of thermal stress. When this is driven by light stress only, it is referred to as photo-bleaching | Lesser, 1997 |
| Degree heating weeks | A measure of heat stress combining the effects of magnitude and duration of SST that exceeds the expected summertime conditions (MMM), accumulated across a rolling 12-week period | Liu et al., 2005 |
| Endolithic microborers | Microbial, boring organisms living within rocks, shells, and coral skeletons | Tribollet, 2008b |
| Marine heatwaves (MHWs) | A period of ≥5 days wherein the temperature is above the 90th percentile of historically observed values for that location for that time of year | |
| MHW hotspots | Localized thermal extremes nested within regional SST anomalies that are not accurately represented using the DHW framework, but fulfil the above criteria for an MHW | This review |
| Mass mortality | An ill-defined term. Previously used to described mortality prevalence of greater than 30% | Hughes et al., 2017 |
| Maximum of the monthly mean (MMM) | The location-specific SST representative of expected summertime conditions, determined as the warmest monthly climatological SST with a baseline period in the late 1980s | Liu et al., 2014 |
| Microbioerosion (corals) | Chemical dissolution of aragonite skeleton by endolithic microborers | Tribollet, 2008b |
| Phase shift | Shifts between alternative stable states of an ecosystem. In coral reefs, this is typically between coral- and algal-dominated benthos | Idjadi et al., 2006 |
| Reactive oxygen species (ROS) | Oxygen radicals produced as by-products of photosynthesis and respiration, with the potential to damage lipids, proteins and DNA: superoxide (O2–), hydrogen peroxide (H2O2), singlet oxygen (1O2), and hydroxyl (OH–) | Murphy, 2009 |
| Sea surface temperature (SST) anomalies | The variation in SST from what is expected to occur at each location at the specific time of year. Expected values are typically defined using a long-term climatology | Liu et al., 2005 |
Common and key terms, and their definitions, used in this review.
In the last 20 years, the prevalence and intensity of mass coral bleaching events triggered by anomalously warm SSTs has increased (; ; Hughes et al., 2018a). For example, on the GBR mass coral bleaching was observed in 1998, 2002, and 2015–2017 (; ; Hughes et al., 2017). Comparisons of the 1998, 2002, and 2015–2017 bleaching events highlighted the unprecedented scale and severity of the most recent event which affected nearly two-thirds of the 2,300 km long system (Hughes et al., 2017). This was driven by an increase in the relative proportion of individual reefs experiencing severe thermal stress (Hughes et al., 2017). These observations are reflective of the global trend in the intensity of coral bleaching events throughout the Anthropocene (Hughes et al., 2018a). The intensity and frequency of marine heatwaves (MHWs) in the same time period has also increased (Oliver et al., 2018). MHWs have recently been defined as a period in which the water temperature is above the 90th percentile for that area’s historical conditions for five or more days, where the climatological threshold is a time-of-year dependent 11-day shifting window (). MHWs represent the most extreme and “rare” incidences of thermal stress relative to a season-dependent historical baseline (). However, this definition has only recently been applied, for the first time, to the study of coral bleaching events (Smale et al., 2019) though this considered the annual accumulation of MHW days rather than individual events.
For over two decades, the degree heating week (DHW) product of the NOAA Coral Reef Watch (Liu et al., 2017) has been the standard metric for measuring, comparing and predicting accumulated heat stress, referenced to the historically warmest time of the year (“summertime”) in coral reef environments. DHWs represent the duration of thermal anomalies experienced by corals, accumulated across a three month period (Liu et al., 2005). In this instance, positive temperature anomalies are calculated above the maximum of the monthly mean (MMM) threshold, which is the temperature of the climatologically warmest month for an area (; Liu et al., 2017). When DHW values reach 4°C-weeks, coral reefs are predicted to experience mild bleaching, while greater than 8°C-weeks has been associated with severe bleaching and widespread mortality (Liu et al., 2005). DHWs allow for the broad tracking of the accumulation of heat in a water body over a relatively long time frame and can be used to infer some physiological heat stress responses (Liu et al., 2005).
The degree heating week approach, while powerful, has not always detected intense, acute events that are able to cause significant coral bleaching, particularly those that are spatially restricted (Weeks et al., 2008; ; ). For example, intense heating in the southern GBR in 2006 caused bleaching in more than 90% of surveyed corals in the Keppel Islands (Weeks et al., 2008) but was insufficient to trigger alerts when relying solely upon the DHW approach due to ocean heating occurring earlier than usual outside of the summer season. Likewise, extreme heating in 2015 on the Dongsha Atoll drove temperatures to 6°C above the climatological mean and the mass mortality of 40% of the local coral population was observed (). The short-lived and localized nature of the heating meant large-scale satellite monitoring did not capture the event and alert systems failed due to a reliance on accumulation of heat over extended periods, which did not occur. In this case the rapid onset of warming within less than a week and persistence of these high temperatures for more than 5 days () would qualify the event as a MHW (). Similarly, the peak of thermal stress on Thursday Island during the 2016 mass bleaching event was not accurately represented when using traditional remote sensing techniques (). Temperatures increased from the climatological baseline to well above the 99th percentile within less than a month, and this persisted for 11 days (), qualifying the event as a strong MHW (). While the accumulated thermal stress in this area eventually peaked at 14°C-weeks in mid-May, this was almost 2 months after the occurrence of the majority of mass mortality (; ; Hughes et al., 2017).
Marine heatwaves do not always translate into a meaningful value for DHWs, and this is particularly relevant when predicting the ecological and physiological outcomes of these events. During the 2011 massive thermal anomaly off the coast of Western Australia, ≥16°C-weeks was recorded across approximately 1200 km along the coast (Moore et al., 2012). The most intense heating, around the Houtman Abrolhos Islands, was also represented by a 95-day MHW () and triggered mass coral bleaching (Smale and Wernberg, 2012). Here, a new “extreme” category of DHWs might complement the existing “mild” and “severe” thresholds and serve to represent MHWs. However, acute and intense summertime MHWs can occur independently of high corresponding DHW values. For example, at the peak of the MHW on Thursday Island in 2016 the corresponding DHW value was approximately six (). In the same study, water temperatures around Lizard Island were recorded as increasing to around the 95th climatological percentile, where they remained for 9 days (). A corresponding DHW value of 4°C-weeks would predict mild coral bleaching, in stark contrast to the observed extent and severity of coral bleaching and mortality around Lizard Island (; Hughes et al., 2017). Using the online Marine Heatwave Tracker1 (Schlegel, 2018), this same event is categorized as a “II Strong” MHW using the classification system proposed by .
In addition to the improved detection of short-lived, intense thermal anomalies, the application of the MHW criteria also allows us to consider thermal stress outside of summer months. As the accumulation of DHWs is based on the exceedance of summertime maxima, this limits application to this season. Yet there is evidence that thermal stress outside of this period can have significant impacts on marine environments and are captured using season-dependent shifting climatological baselines (Weeks et al., 2008; , ). But while it is known that cold temperatures can lead to cold water coral bleaching (; Lirman et al., 2011), as yet we have little information on the effects of positive winter anomalies on corals. examined seasonal changes in bleaching thresholds for the coral Pocillopora damicornis and found the thresholds decreased by only 1°C from summer to winter, suggesting that seasonal acclimatization may not reduce thresholds to such an extent that winter bleaching will occur during a winter MHW. There is, however, evidence that water temperatures in the winter can affect coral disease progression and susceptibility. Sato et al. (2009) identified a correlation between lower winter temperatures and the lower infectivity and progression in black band disease while a large scale temporal analysis by found that mild winters (i.e., neither anomalously hot or cold) frequently preceded outbreaks of coral white syndrome in the following year. The observation that disease outbreaks did not generally follow warmer winters suggest that winter MHWs have the capacity to significantly influence coral physiology in the long term. This is an important area for future exploration given that coral tissue biomass is higher in the winter and early spring () and influences coral bleaching responses (). These periods are likely important for resource provisioning leading into coral spawning and summertime.
Examining thermal stress in coral reef environments using a MHW approach can therefore add a new dimension to how we understand, detect and measure coral bleaching and mortality events to the benefit of our present alert systems. The cases outlined here demonstrate firstly that extreme and small scale coral bleaching and mortality events, which do not accumulate DHWs above thresholds needed to trigger alerts, can be identified using MHW criteria. When used in conjunction with DHWs, this may improve our ability to predict fine scale ecological patterns during mass coral bleaching events. Secondly, that mismatches between low DHW values and severe ecological degradation can be reconciled by applying MHW criteria in explaining causative factors of mass coral mortality. This evidence provides a means to improve the accuracy of our predictions of the responses of reef communities when these values are considered alongside an understanding of the biological responses to the thermal conditions. It is important to consider MHWs as acute, intense events disparate from those characterized by chronic heat accumulation, and independent of the existing DHW scale. As summertime MHWs are often nested within broader thermal anomalies, the term “MHW hotspots” as used in this review represents the most extreme patches of thermal stress, and the distinct ecological and physiological responses that occur within these.
The Evolution of MHW Hotspots
Marine heatwaves hotspots are often the result of combined regional heating and local weather patterns, which interact to promote the rapid accumulation of heat (Skirving et al., 2006; MacKellar and McGowan, 2010; Wernberg et al., 2012; ; ). Abiotic factors that influence these events include tidal cycles, calm winds, clear skies and low water flow, which act to amplify regional thermal stress on the scale of individual reefs (Figure 1; Skirving et al., 2006; MacKellar and McGowan, 2010; ; Raymundo et al., 2017; ). Potentially the most commonly cited driver of thermal extremes in coral reef environments is a drop in wind speed (; ; ). Wind influences most components of the oceanic heat budget (Figure 1; Talley et al., 2011; Lowe and Falter, 2014), in part through how it affects currents and wave action (; MacKellar et al., 2013). However, these latter factors are not always forced by local wind patterns and can have distinct effects upon heat accumulation and physiological responses (Nakamura, 2010; Lentz et al., 2016). There is therefore often a mismatch between the scale of a MHW hotspot and the resolution of available satellite imagery, due to the influence of these abiotic factors at the reef-scale. The confluence of these physical drivers is physiologically significant for reef corals and determines the severity of the bleaching process. High insolation maximizes the heat and light stress experienced by corals, which act synergistically to drive and exacerbate coral bleaching and mass mortality in time frames directly related to the intensity of environmental stress (Jones et al., 1998; Lesser and Farrell, 2004; Skirving et al., 2017).
FIGURE 1
The highest potential for heat loss from a water body results from evaporative cooling i.e., latent heat flux (Qe) (Figure 1; Talley et al., 2011). Weller et al. (2008) attributed coral bleaching on the GBR in 2001/2002 primarily to low wind and resultant low evaporation. Indeed, evaporative cooling has been shown to be strongly coupled to wind speed because of how this affects the air-sea temperature difference (Wu et al., 2007; MacKellar and McGowan, 2010; MacKellar et al., 2013; ). When wind speeds drop to negligible levels, evaporation quickly leads to high humidity at the air-sea interface which reduces the potential for further evaporative cooling (Wu et al., 2007; Weller et al., 2008; MacKellar and McGowan, 2010). Additionally, this increases the air’s heat capacity and promotes air-to-sea heat transfer through sensible heat flux (Qh) (Figure 1; Weller et al., 2008; ). Reductions in wind speed often precede increases in SSTs and a number of case studies have identified a reduction in wind speed with subsequent increases in humidity and heat accumulation. Two small scale bleaching events, at Lee Stocking Island in 1990 (Smith, 2001) and on the sub-tropical Heron Reef in 2009 (MacKellar and McGowan, 2010), linked a drop in wind speed below 3 ms–1 to an increase in humidity and reduction in evaporative cooling. In the case of the latter, the daytime maximum temperature increased to >34°C in a matter of days and caused short term coral bleaching (MacKellar and McGowan, 2010). Similarly, the most extreme temperatures recorded at a depth of 6.5 m by , in the southern Arabian Gulf, were strongly correlated with wind speeds below a local threshold of 4 ms–1. These values, as well as that identified by (2.8 ms–1), lend credence to the threshold chosen by NOAA (3 ms–1) in defining doldrum-like winds in relation to coral bleaching (Liu et al., 2012).
On a larger scale, a reduction in wind speed was linked to widespread warming during the 2001/2002 mass bleaching event on the GBR (Weller et al., 2008) and the 2015 thermal anomaly in the South China Sea that underpinned the mass mortality event on the Dongsha Atoll (). These studies also identified increased air-to-sea sensible heat flux resulting from increases in humidity. In the converse scenario, strong winds promote cooling and are able to reduce temperatures by several degrees, especially at night (MacKellar et al., 2013). This is thought to be an important cellular recovery period after damage sustained by daytime maxima (Roberty et al., 2015). Thus, negligible wind speeds and associated rapid heat accumulation not only increases daytime heat stress but also possibly reduces the potential for night-time recovery.
Accompanying doldrum-like wind speeds is a reduction in sea surface turbulence which would otherwise promote cooling. A flat ocean surface acts as a viscous boundary layer at the air-sea interface and significantly limits sea-to-air heat flux (Moum and Smyth, 2001; ). This promotes the accumulation of heat in surface waters and thermal stratification in the water column (Van Hooidonk et al., 2013; Lowe and Falter, 2014; Zhang et al., 2016). Exacerbating this effect, flat seas generate little to no downwelling (Moum and Smyth, 2001). In contrast, strong winds generate shear-induced turbulence at the air-sea interface which leads to small pockets of cool water that sink down through the upper layer (Moum and Smyth, 2001; ). This downwelling destabilizes a stratified water column and aids in distributing heat from insolation away from surface waters (Figure 1; Moum and Smyth, 2001; Lowe and Falter, 2014). A lack of wind-generated wave action therefore promotes a positive feedback loop in which heat accumulation stabilizes thermal strata which in turn allows for a greater heat load in surface waters (Figure 1). Oceanic swell can generate wave-related surface cooling independent of wind conditions; however, the rapid dissipation of wave energy by fore reef environments limits the spatial extent of this mechanism (Lowe and Falter, 2014). Wind-driven turbulence, on the other hand, can extend into reef lagoons, and cause significant cooling by vertical mixing (MacKellar et al., 2013).
A lack of wind forcing and wave action often results in low levels of water circulation and heat exchange with the open ocean (; Lentz et al., 2016; ). Advection (i.e., horizontal water movement, Qv), or a lack thereof, has been proposed as a key determinant of the accumulation of heat on coral reefs (Figure 1; MacKellar et al., 2013; Lowe and Falter, 2014). Flushing reefs with cool water from deeper surroundings can lower daytime maximum temperatures and reduce diurnal variation (; MacKellar et al., 2013; ). Additionally, currents have been shown to promote vertical mixing independent of wave-driven down-flow (). Circulation is controlled by surface wind-driven currents (Lowe and Falter, 2014), waves (Lentz et al., 2016), and tidal cycles (MacKellar et al., 2013). The more sheltered the reef environment, the more dependent it is upon circulation driven by wind and wind-generated waves (; Lentz et al., 2016). In MHW hotspots, the lack of wind and waves therefore limits circulation and advective cooling (; Van Wynsberge et al., 2017). As a result, water has high residency time, pools over the reef and heats up rapidly (; Van Wynsberge et al., 2017). Tidal flushing can, in some cases, offset heat accumulation considerably (MacKellar and McGowan, 2010; Lowe and Falter, 2014) while neap tides and weak intertidal currents have been identified as causal factors for intense heating (). Conversely, mass mortality has also been associated with large spring tides during regional low-stand periods that drove increased subaerial exposure (Raymundo et al., 2017). Therefore, the effect of tidal cycles on coral bleaching and mortality is likely to be highly dependent upon a reef’s bathymetry and tidal range.
Doldrum-like winds and the associated physical outcomes are often representative of broad areas of high atmospheric pressure (MacKellar and McGowan, 2010; ; ). The consequence is increased solar irradiance (QS) (Figure 1), which is the primary source of heat input on coral reefs, and has been linked to the rapid onset of thermal stress (; MacKellar et al., 2013; ). High irradiance is also a primary source of stress as it drives oxidative stress in symbiotic algae through the production of reactive oxygen species (ROS) (Jones et al., 1998; ; Krug et al., 2013). The effect of high cloud cover in reducing coral bleaching intensity is well documented (; Zelinka and Hartmann, 2010; Hughes et al., 2017), particularly when tropical cyclones pass over coral reefs, and simultaneously cool surface waters through wind exposure (Manzello et al., 2007; ). Water column stratification can increase light stress by reducing light attenuation of suspended particulates (through absorption and/or backscatter) in the surface layers (Manzello et al., 2004; Zepp et al., 2008). The opposite effect (i.e., suspended particulates reducing light stress) is apparent when we observe high coral bleaching tolerance on turbid inshore reefs compared to offshore reefs with high water clarity (Morgan et al., 2017). Additionally, flat seas minimize light scattering through surface turbulence and so maximize the intensity of light experience by corals and their symbionts. Combined with the high accumulation of heat, increased light is able to rapidly overcome corals’ mechanisms of physiological resilience in short time frames.
Ecological Consequences of MHW Hotspots
The impact of MHW hotspots on coral populations can be ecologically distinct from what is understood of traditional bleaching events. The first compelling evidence for MHW hotspots leading to distinct ecological outcomes, is that they cause widespread bleaching and mortality in corals that would normally be categorized as thermally tolerant “winners” during milder events (Loya et al., 2001; ; Hughes et al., 2018b). In their study of the Dongsha Atoll, used coral cores of a thermally tolerant Porites sp. to examine historical bleaching in the reef lagoon. In the previous 100 years, no more than 50% of the population had bleached during any one event (). In contrast, 100% of this species bleached during the acute 2015 event where temperatures peaked at 6°C over the climatological mean (). In a similar case, examined the responses of Acroporids during the extreme 2016 anomaly on Lizard Island. The authors highlighted how species that exhibited high thermal tolerance during previous mass bleaching events on the GBR in 1998 and 2002 experienced widespread and indiscriminate bleaching in mid-to-late March (). This coincided with the temperatures spiking above the 95th climatological percentile (). The ability for extreme, acute thermal stress to overcome the protective mechanisms of otherwise heat tolerant species was also evident in regions where corals have adapted to naturally extreme environments. Corals in the Arabian Gulf have some of the highest bleaching thresholds, partly due to the selective pressure of maximum summer temperatures exceeding 34°C annually (Riegl et al., 2011). Between August and September 2017, these thermally tolerant coral populations experienced mass bleaching and mortality following up to 20 consecutive days above their lethal threshold of 35.5°C, less than two degrees Celsius above the climatological summertime maximum (Shuail et al., 2016; ). Even in the context of this naturally warm environment, the non-selective bleaching of thermally tolerant coral populations was considered unusual and extreme (). Similarly, during the 2014–2017 global coral bleaching event (), mass bleaching of thermally tolerant corals in the southern Kimberley region of northwestern Australia was observed (Le Nohaïc et al., 2017). This population is considered to be relatively resistant to climatic extremes (Schoepf et al., 2015) and indeed this was the first recorded instance of coral bleaching at these extreme, inshore reefs (). However, while heat stress of 11.4°C-weeks drove this extreme response, further north reefs exposed to 14.8°C -weeks showed little to no bleaching (). This supports the notion that DHWs are not accurately predicting ecological responses during these extreme events.
Finally, the rate of heating during a MHW hotspot can drive uncharacteristically rapid onset of bleaching and mortality. For example, water temperatures in the Keppel Islands, 2006, reached summertime maxima in December as opposed to February which would normally be the result of long-term accumulation of heat (Weeks et al., 2008). By mid-January, between 77 and 95% of coral colonies exhibited bleaching () due to both the rate and seasonal timing of heat accumulation (Weeks et al., 2008). During the 2016 event on Lizard Island, healthy coral-dominated reefs transitioned through mass bleaching and mortality to algal-domination in approximately 6 weeks (; Hughes et al., 2017). This timeline is remarkably similar to that recorded on the Dongsha Atoll, where mass mortality occurred in less than 6 weeks (). The accelerated rate of mortality associated with the rapid accumulation of heat is further exemplified by observations of coral mortality in Iriomote 2 weeks after the initial onset of thermal stress driven primarily by doldrum-like wind speeds (). These timescales are in contrast to normal bleaching events, where coral bleaching typically occurs following several months of heat stress (Weeks et al., 2008; Liu et al., 2014). In the most extreme examples, this accelerated heating can even lead to coral mortality without prior bleaching as observed on the GBR in 2016 (Hughes et al., 2017). This is likely a combined result of increased heat damage to coral host cells and higher in situ degradation of symbionts observed during extreme thermal stress (Strychar et al., 2004; Strychar and Sammarco, 2009).
These ecological observations of MHW hotspots overcoming thermal tolerance and causing mass bleaching and/or mortality in short time frames indicates that mechanisms usually associated with coral acclimatization or resistance to high temperatures are being overcome during these extreme events. Typical coral bleaching events often result in the emergence of thermally tolerant “winners” and thermally susceptible “losers” within a coral reef community (Loya et al., 2001), selecting for those most thermally tolerant coral species (see Table 2). When subjected to extreme MHW hotspots however, the interspecific differences in coral thermal tolerance that underpin this paradigm appear to be less important in shaping community responses, given the extensive bleaching and mortality observed in putatively tolerant coral species.
TABLE 2
| GENUS | SPECIES | ||||
| Genus | Tolerance | Species | Tolerance | Location | Source |
| Acropora spp. | Low | A. digitifera | Low | Okinawa, Japan | Loya et al., 2001; Van Woesik et al., 2004 |
| A. gemmifera | Low | Okinawa, Japan | Van Woesik et al., 2004 | ||
| A. hyacinthus | Low | GBR, Aust. | |||
| A. millepora | Low | GBR, Aust. | ; | ||
| A. tenuis | High | GBR, Aust. | |||
| Acropora sp. | Low | Mombasa, Kenya | McClanahan et al., 2004 | ||
| High | GBR, Aust. | ||||
| Agaricia spp. | Low | A. agaricites | High | Jamaica, Caribbean | |
| A. lamarcki | Low | ||||
| Favites spp. | High | F. halicora | High | Okinawa, Japan | Loya et al., 2001 |
| Goniastrea spp. | Low | G. aspera | High | Okinawa, Japan; Phuket, Thailand | Loya et al., 2001; |
| G. pectinata | High | Okinawa, Japan | Loya et al., 2001 | ||
| Leptastrea spp. | High | L. purpurea | High | Okinawa, Japan | Loya et al., 2001 |
| L. transvera | High | Okinawa, Japan | Loya et al., 2001 | ||
| Montastrea spp. | High | M. annularis (Orbicella annularis) | Low | Jamaica, Caribbean | |
| M. cavernosa | High | ||||
| Montipora spp. | Low | M. aequituberculata | Low | Okinawa, Japan | Loya et al., 2001 |
| M. digitata | High | GBR, Aust. | Nitschke et al., 2018 | ||
| Pavona spp. | Low | P. minuta | High | Okinawa, Japan | Van Woesik et al., 2004 |
| P. varians | |||||
| P. clavus | Low | Phuket, Thailand | Phongsuwan and Chansang, 2012 | ||
| Platygyra spp. | Low | P. daedalea | High | GBR, Australia | |
| P ryukuensis | High | Okinawa, Japan | Loya et al., 2001 | ||
| Pocillopora spp. | Low | P. damicornis | Low | Okinawa, Japan | Loya et al., 2001 |
| High | Eilat, Red Sea | ||||
| P. verrucosa | High | Okinawa, Japan | Van Woesik et al., 2004 | ||
| Porites spp. | High | P. attenuata | Low | Okinawa, Japan | Loya et al., 2001 |
| P. cylindrica | Low | Loya et al., 2001 | |||
| High | Van Woesik et al., 2004 | ||||
| P. lutea | High | Phuket, Thailand | |||
| P. nigriscens | Low | Okinawa, Japan | Loya et al., 2001 | ||
| Porites sp. | Low | Mombasa, Kenya | McClanahan et al., 2004 | ||
| High | GBR, Aust. | ||||
| Stylophora spp. | Low | S. pistillata | Low | Okinawa, Japan | Loya et al., 2001 |
| High | Gulf of Aqaba, Red Sea | Krueger et al., 2017 | |||
Examples of coral genera and species reported to have high or low thermal tolerance.
Genera-specific susceptibilities were defined according to the meta-analysis performed by Swain et al. (2016). The threshold used to distinguish high and low thermal tolerance was set at the total sample median (23.17) of the Bleaching Response Indices calculated for the 374 taxa used in Swain et al. (2016). Individual species’ susceptibility is commonly defined by each taxon’s response to a natural bleaching event, and so is relative to the total community response to said event. Thermal tolerance is influenced by location and environmental history, but shows taxon-specific consistency across locations (McClanahan et al., 2004; Swain et al., 2016).
Coral Thermal Stress Responses and MHWS
Thermal stress events have a variety of impacts on the coral photo-endosymbiotic organism. These range from sub-lethal effects, which may reduce fitness, to mortality that is most often associated with starvation due to the breakdown of the coral-algal symbiosis (; ; Tables 1, 3). Coral species are generally described in categories of thermal stress susceptibility, ranging from slow growing species with massive growth forms, such as Porites spp., which have high tolerance to thermal stress to fast growing branched species, such as Acropora spp., which are considered to have low tolerance (Table 2). The thermal tolerance of a species in a specific coral reef location is determined by a complex interplay of factors. While there is some consistency over large spatial scales (Table 2), the current and historical environmental conditions at a particular reef drive intraspecific physiological and morphological differences. These include: characteristics of the corals growth form and skeletal phenotype (massive vs. branching morphology) (Loya et al., 2001); capacity for and extent of heterotrophic feeding (); dominant symbiont type (e.g., thermally tolerant clade D vs. susceptible symbiont clade C) (); acclimatization potential (); and adaptive tolerance to thermal stress (). There is a spectrum of traditional responses by the coral animal to thermal stress, ranging from short-lived photobleaching, where photosynthetic efficiency is reduced often accompanied by a reduction in photosynthetic pigments, and through to mortality of the host animal from starvation (Table 3). This spectrum has been used to model the future characteristics of reefs under climate change scenarios under the assumption that, in general, as thermal stress accumulates within an event corals progress through each stage of this scale at different rates reflective of the animals’ resilience and the severity of the stress (). This is generally consistent across different bleaching events, although there are exceptions and there is mounting evidence that animals’ resilience can be altered within one generation due to acclimatization (). However, under conditions concomitant with a MHW hotspot, this progression of the thermal bleaching response is no longer evident. Instead, the responses typical of acclimatization (see Table 4) are absent, corals exhibit signs of direct heat damage and mortality can happen in a matter of days (Leggat et al., 2019), potentially without prior bleaching (Hughes et al., 2017). This is due to the intensity of these thermal stress events overwhelming corals’ ability to cope in the short term, bypassing the meta-organism’s bleaching process and instead resulting in heat-induced mortality of the coral animal. This is a distinct physiological outcome of extreme thermal stress compared to how we traditionally consider bleaching-induced mortality (i.e., the progressive breakdown of symbiosis leading to mortality from starvation).
TABLE 3
| Healthy | Photo-bleaching | Traditional thermal bleaching, mild (i.e., DHW > 4) | Traditional thermal bleaching, severe (i.e., DHW > 8) | Summertime marine heatwave, heat damage | |
| Damage to photosynthetic pigments | × | ✓ | ✓ | ✓ | ✓ |
| Reduction in symbiont density | × | × | ✓ | ✓ | ✓ Highest |
| Whole colony bleaching (>50% reduced symbiont density) | × | × | ✓ | ✓ | ✓ |
| Tissue damage | × Polyps intact | × Polyps intact | × Polyps intact | ✓ Polyps possibly damaged | ✓ Polyps degraded |
| Cell death | × | × | ✓ Minimal | ✓ Widespread apoptosis, starvation | ✓ Widespread necrosis, may precede whitening |
| Colony recovery | N/A | ✓ Fastest | ✓ | ✓ Slowest, tissue re-modeling | × |
| Mass mortality | × | × | × | ✓ Gradual, across months | ✓ Highest, rapid, within weeks |
| Reef recovery | N/A | N/A | ✓ | ✓ Survival and re-growth | ✓ Slowest Recruitment |
The range of ecological and physiological responses of corals to varying degrees of environmental stress.
TABLE 4
| Cellular component | Acclimatory response | Source |
| Heat shock proteins (HSPs) | Increased production and activity of molecular chaperones Hsp 60, 70, and 90 to ensure correct digestion of degraded proteins and folding of new proteins within the Endoplasmic Reticulum. Core component of the Unfolded Protein Response | Leggat et al., 2011; Rosic et al., 2011; Seveso et al., 2014, 2016 |
| Enzymatic antioxidants | Increased production and activity of SOD, APX, CAT, GR, and DMSO (see Table 1) in order to counter the accumulation of oxygen radicals and prevent cellular damage | Krueger et al., 2014, 2015; Roberty et al., 2015; |
| Non-enzymatic antioxidants | Increased genetic expression of cytochrome P450 and heat shock proteins, with putative antioxidant properties | Rosic et al., 2010 |
| D1 repair and de novo synthesis (symbiont) | Increased in situ repair and de novo synthesis of D1 reaction centre proteins that are damaged during photoinhibition by combined high light and high temperature | Takahashi et al., 2008, 2009, 2013; |
| Lipid membrane composition | Composition shift toward higher saturation of Polyunsaturated Fatty Acids (PUFAs) in the lipid membrane, to increase resistance to oxidative stress | Tchernov et al., 2004 |
| Photoprotective proteins and MAAs | Higher bio-synthesis of mycosporine-like amino acids (MAAs) and photoprotective proteins in both coral host and algal symbiont | ; ; ; Rosic and Dove, 2011 |
| Non-photochemical quenching (symbiont) | More de-epoxidation of xanthophyll pigments in order to dissipate excess excitation energy | ; Middlebrook et al., 2010 |
| Unfolded protein response | Generalized response to the accumulation of degraded proteins. Acts to slow and minimize errors in protein synthesis | Walter and Ron, 2011; Ruiz-Jones and Palumbi, 2017; Traylor-Knowles et al., 2017 |
Demonstrated acclamatory responses of coral host and/or symbiotic algal cells to thermal stress.
See Table 1 for antioxidant abbreviations.
While both the coral host and its symbiont are physiologically challenged by the temperature stress associated with historical coral bleaching events (), the symbiont has been considered as the more thermally sensitive partner in the symbiosis (Jones et al., 1998; ; Krug et al., 2013). This widely accepted understanding of coral bleaching has driven substantial research into determining the mechanisms underpinning damage to the endosymbiotic photosystems, a process generally described as photo-bleaching or light stress-induced symbiosis breakdown. The prevailing theory around the primary cause of coral bleaching is the production of ROS following heat induced impairment to photosynthesis within the symbiont (Table 1; Jones et al., 1998; Takahashi et al., 2009), although mitochondrial damage in both host and symbiont has also been implicated (). ROS are natural products of the series of redox reactions that form electron transport chains in both photosynthesis and respiration (; Murphy, 2009). There are numerous ROS species generated through multiple molecular pathways that have the potential to disrupt cellular homeostasis through the oxidation of lipids, proteins and DNA (Table 1; Lesser, 1997; Jones et al., 1998). As such, cells have evolved natural antioxidant mechanisms to neutralize ROS and prevent oxidative stress (see Table 4). For example, during thermal stress, there is an increased production and activity of antioxidants in the symbiotic algae, in response to the accumulation of ROS that arises from the disruption to electron transport (Krueger et al., 2014, 2015; Roberty et al., 2015).
Increased temperature is also characterized by higher frequencies of apoptosis (cell death) and the upregulation of cellular apoptotic pathways in the coral animal. Apoptosis is a highly conserved evolutionary response (Quistad et al., 2014; Moya et al., 2016) that has evolved to remove damaged cells and prevent the further damage (). This is in contrast to uncontrolled cell necrosis in which cells degrade, swell and burst, to the detriment of neighboring cells (). Apoptosis has been observed to occur in both coral and algal cells during the very early stages of thermal stress (; , ; Strychar and Sammarco, 2009) and initially is localized to the gastrodermal cells that contain symbionts, suggesting that this is triggered through the initial photo-bleaching stage of the bleaching process (, ). While apoptosis is a stress response to cellular damage that results in the removal of host cells, this process increases the potential of the individual coral colony to survive by maximizing resources for the surviving cells and removing sources of ROS (; Tchernov et al., 2011; Kvitt et al., 2016).
Upregulation of antioxidants, the apoptotic pathway and other stress responses, such as increased heat shock protein production for protein repair and replacement (Table 4; Walter and Ron, 2011; Seveso et al., 2014; Ruiz-Jones and Palumbi, 2017), are evolutionary mechanisms designed to increased colony survival during thermal stress. Together with species-specific characteristics, such as tissue thickness, skeletal morphology and feeding behavior, these mechanisms drive interspecific variability in coral stress responses (through acclimatization) as heat stress accumulates. Therefore, in canonical bleaching events where summertime thermal stress drives coral bleaching after several weeks to months, the meta-organism’s thermal tolerance is directly determined by the cellular processes and species-specific traits that underpin inherent thermal tolerance and the potential for the induction of further protective mechanisms (i.e., acclimatization) (; ). These processes ultimately drive differential interspecific responses to thermal stress and thus determine how coral communities are affected by coral bleaching events. Under the extreme conditions of summertime MHW hotspots, this relationship between temperature stress and bleaching susceptibility becomes less clear as the severity undermines the capacity for acclimatization. When exposed to sufficiently large and rapid onset temperature anomalies, the induction of acclamatory mechanisms is bypassed or impaired and inherent thermal tolerance is overwhelmed. The hosts’ molecular and cellular responses to damage are either inhibited or insufficient to repair the extent of damage as it occurs within the cells. For example, a uniformly sharp decline in the activity of the antioxidant enzymes, glutathione reductase (GR) and superoxide dismutase (SOD), was described following exposure of zooxanthellae to 33°C for 6 days, irrespective of whether the symbiont was considered thermally tolerant or susceptible (Krueger et al., 2014). A similar thermal exposure (33.5°C for 6 days) of the zooxanthellate sea anemone Aiptasia also resulted in a reduced frequency of apoptosis but more frequent necrosis in both host and symbiont (). In the coral Seriatopora caliendrum, a collapse in the activity of heat shock protein 60 was seen in just 18 h after a sudden temperature increase to 33°C (Seveso et al., 2016). This inhibition of the apoptotic protective mechanism, in conjunction with reduced antioxidation and cellular repair, indicates damage to, or overwhelming of, cellular acclimatory mechanisms and the rapid coral mortality of species with both high and low tolerance indicates a failure of protective mechanisms to safeguard the animal against heat-induced cell death. This scenario has recently been observed in a number of locations where coral mortality during extreme thermal stress is unrelated to historical community responses (Schoepf et al., 2015; ; ; ; Le Nohaïc et al., 2017). This evidence demonstrates that under severe and rapid heating associated with MHW hotspots, the response of the coral animal is distinct from how we currently define coral bleaching and associated mortality.
Post-Mortality Processes Following MHWS
Given that rapid and extensive cell (and thus colony) mortality is a direct consequence of extreme thermal stress and occurs in a distinct fashion, this suggests that post-mortality processes on coral colonies may also be distinct. This is especially the case when thermal stress conditions persist after rapid coral mortality, which is likely given the short time frames in which MHW hotspots can drive ecological degradation. Recent evidence presented by Leggat et al. (2019) demonstrates that extreme, rapid onset thermal stress, and the associated heat-induced mortality, together with local oceanographic conditions (doldrums, low water flow, and high light intensity) promote rapid microbial bioerosion of coral skeletons by phototrophic microbes, resulting in a degradation of reef structural frameworks at rates hereto unprecedented (Table 5). The cause is the microbial bloom formation of endolithic microborers, which reside within the skeletons of living corals skeleton and colonize newly exposed substrates (i.e., recently dead corals). This study represents the first time that the effect of coral mortality and thermal stress upon microbial bioerosion has been investigated, and suggests that MHW hotspots have an effect upon the physical reef structure, as well as the biological community.
TABLE 5
| Substrate | Environmental conditions | Rate (g CaCO3 m–2 month–1) | Source |
| Mollusc sediment | Ambient, reef lagoon | 29.2 | Tudhope and Risk, 1985 |
| Mollusc shell (Strombus gigas) | Experimental inorganic nutrient enrichment, in situ | 37.6 | |
| Mollusc shell (Strombus gigas) | Experimental inorganic nutrient enrichment, in situ | 33.2 | |
| Mollusc shell (Strombus gigas) | Experimental inorganic nutrient enrichment, in situ | 49.4 | |
| Mollusc shell (Tricadna sp.) | Inshore reef subject to terrestrial discharge (river) | 11.4 | Mwachireya et al., 2018 |
| Coral block (Porites sp.) | Volcanically acidified reef (pCO2 = 502 μatm) | 126.6 | |
| Coral block (Porites sp.) | Oligotrophic offshore reef (Osprey Reef) | 111.7 | Tribollet et al., 2002 |
| Coral block (Porites sp.) | Oligotrophic offshore reef (Osprey Reef) | 112.5 | Tribollet, 2008a |
| Coral block (Porites sp.) | Experimental pCO2 increase, ex situ (pCO2 = 750 μatm) | 39.0 | Tribollet et al., 2009 |
| Coral block (Porites sp.) | Oligotrophic offshore reef (Osprey Reef) | 116.7 | Tribollet and Golubic, 2005 |
| Micritic limestone | Ambient, reef lagoon | 43.3 | Vogel et al., 2000 |
| Coral block (Porites cylindrica) | Experimental pCO2 + temperature increase, ex situ (pCO2 = 1010 μatm; temp = control + 4°C) | 239.6 | Reyes-Nivia et al., 2013 |
| Coral colony fragment (Acropora aspera) | Experimental, marine heatwave induced mortality (DHW > 8) | 1584 | Leggat et al., 2019 |
Maximum rates of microbioerosion reported in theliterature, in different substrates and under a variety ofenvironmental or experimental conditions (Leggat et al., 2019).
Endolithic phototrophic microbes are arguably the second most significant bioeroders on coral reefs, after parrotfish (; Perry et al., 2014). Knowledge of this microbial community is extremely limited, but it is already recognized as able to undermine structural stability over longer time frames (Tribollet, 2008a; Tribollet and Golubic, 2011; Silbiger et al., 2015; ) and is considered an important driver of reef-wide shifts toward net erosion (Perry and Morgan, 2017). The evidence presented by Leggat et al. (2019) changes how we currently understand the short- and long-term consequences of thermal stress on a reef, though the processes underlying this outcome remain to be elucidated (Figure 2). Studies over longer time frames have shown that increased light, temperature, pCO2 and nutrient load accelerate rates of microbial bioerosion (Tribollet and Golubic, 2005; ; Tribollet et al., 2009; Reyes-Nivia et al., 2013), through promoting the growth of primarily endolithic eukaryotic algae. The rapid mortality during a MHW hotspot represents a rapid shift in conditions within the otherwise stable endolithic microenvironment, changes to which the resident microbes can rapidly acclimatize (, ). Increased light intensity, due to the loss of coral symbionts that otherwise attenuate incoming irradiance, high water temperatures that drive faster metabolism and growth, and a higher availability of nitrogen through rapid tissue decomposition that supports greater biomass, are all likely to play roles in driving increased microbial bioerosion (Figure 2).
FIGURE 2
While there is evidence of MHW hotspots accelerating microbioerosion, and a theoretical framework to support this, what remains unclear is how microbioerosion is influenced by less severe and/or rapid coral bleaching and mortality events. During a canonical coral bleaching/mortality event, ecological degradation evolves over a longer time frame compared to MHW hotspot driven mass mortality as described above. This has a number of possible implications for the process of microbioerosion. Firstly, as coral mortality and the subsequent bloom formation of phototrophic microbes is spatially more patchy, these patches of algal overgrowth can more easily be grazed down by reef herbivores. On the other hand, if a large population of corals dies within a very short time frame then the ensuing growth of microbial algae over a large area could exceed rates of herbivory. This is especially true of endolithic algae already living within coral skeletons (as opposed to colonizers) that only excavating herbivores, such as parrotfish, are able to graze upon ().
Secondly, given that canonical coral mortality events tend to occur toward the end of the summer season after months of heat accumulation and stress, algal microborers are exposed to warm, bright summer conditions for less time before the season ends. In contrast, if a MHW hotspot causes mass mortality in the early summer months [e.g., Weeks et al. (2008)] then microborers have a full summer of ideal conditions for growth and bioerosion. We emphasize here that the accelerated microbioerosion associated with MHW hotspots is, as we currently understand it, an acute effect. It is unknown whether these accelerated rates persist in the long term, though the effects of rapid degradation in reducing structural complexity are likely to persist given that this physical characteristic of coral reefs is otherwise relatively stable over time ().
Finally, the extremity of physical conditions during MHW hotspots that drive rapid ecological degradation would increase the metabolism and growth of phototrophic microbes more so than the comparatively milder conditions of canonical coral mortality events. Together, these characteristics of MHW hotspot driven mass mortality suggest that rapid erosion of the physical reef framework is likely to be a product of extreme thermal stress events, but further research into the effects of thermal stress and coral mortality upon microbial bioerosion is needed to support this.
Given the negative effect of MHW hotspots upon reef structural complexity, we can expect this acute process to affect the long term recovery of affected coral reefs. In our current understanding of coral bleaching events, the recovery of surviving bleached corals depends on the replenishment of symbionts within the intact host, and the re-growth and propagation of these “winners” drives reef-scale recovery. Following events resulting in mass mortality, reef recovery depends upon successful larval recruitment (Idjadi et al., 2006; ; ), and the suppression of algal competition (; ; ). These factors together influence the likelihood of an ecosystem-wide phase shift (Table 1) toward an algal reef and an alteration to ecosystem function (, ; Stuart-Smith et al., 2018).
An important component of both successful recruitment and the suppression of algal competition is the structural complexity of the reef (Vergés et al., 2011; ; ). For example, topographic complexity has been shown to support higher abundances of settled larvae by presenting more opportunity for refuge from predation (; ; Rogers et al., 2014). Similarly, herbivory is a core driver of reef recovery (; ) and is promoted by structural complexity (Vergés et al., 2011). Indeed, a loss of structural complexity can effectively predict the probability of a coral-algal phase shift following mass mortality (), as well as the long term recovery trajectory of coral populations (Robinson et al., 2019a) in part due to concurrent changes in the composition of fish communities (; Robinson et al., 2019b) and the level of larval recruitment (; ).
The effect of MHW hotspots upon herbivore biomass and abundance likely depends upon the examined functional group and the time frame during which we consider changes. In the short term, MHWs have been observed to result in the mass mortality of benthic herbivores, which can be significant grazers of turf and macroalgae (; Wernberg et al., 2012). A key example of this is the 2011 MHW in Western Australia which caused, in one location, 99% mortality in a herbivorous benthic gastropod (Smale et al., 2017). Herbivorous fish often increase in abundance in the months and years following thermal stress events (; Wernberg et al., 2012). However, given the short time frames in which algal overgrowth and coral-algal phase shifts are occuring during MHW hotspots (<2 months) (; Hughes et al., 2017), this effect is either delayed with respect to the phototrophic microbial bloom or insufficient to prevent rapid phase shifts. In fact, in the long term, overall bioerosion may increase in the months following a MHW hotspot due to a higher relative and absolute abundance of excavating fish herbivores (Pratchett et al., 2008; Stuart-Smith et al., 2018) which can be the biggest source of bioerosion in reef environments (; Perry et al., 2014). The three-way interaction between herbivory, microbioerosion and MHW hotspots needs further investigation but we hypothesize that short-term increases in microbioerosion may then be followed by higher macrobioerosion by excavating fish. While a number of questions remain to be resolved regarding this process, these studies highlight the potential for MHW hotspots to impair long term recovery by leading to a rapid degradation of structural complexity (Figure 2).
Conclusion
Our current understanding of the responses of corals to thermal stress, and our predictions of how they will respond in the future are based upon historic bleaching events under which coral and reef degradation is progressive as stress accumulates. However, the emergence of summertime MHW hotspots, the extreme nature of which have no historical counterparts, fundamentally changes how we understand the consequences of climate change in regards to corals reefs worldwide. They result in distinct molecular, cellular and microbial responses, and drive rapid large-scale coral mortality and decay in atypical timeframes. These devastating impacts are occurring irrespective of historical temperature and bleaching regimes, and the long-term ecological consequences of these large-scale mortality events are only now being documented. As such we propose that acute, intense summertime MHW hotspots need to be recognized as a new category of thermal stress event in coral reefs, distinct from the canonical DHW scale that has historically been used to describe bleaching-induced mortality in recent decades.
Statements
Author contributions
AF, TA, SF, and WL developed the concept for the manuscript. AF wrote the original draft of the review which was edited and expanded upon by TA, SF, and WL.
Funding
This research and the authors herein were supported by an Australian Research Council Discovery Project Grant (DP180103199).
Acknowledgments
The authors would like to acknowledge Prof. Silvia Frisia and Assoc. Prof. Danielle Verdon-Kidd for comments on the original manuscript. The scientific results and conclusions, as well as any views or opinions expressed herein, are those of the author(s) and do not necessarily reflect the views of NOAA or the Department of Commerce.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The reviewer SW declared a past co-authorship with one of the authors SH to the handling Editor.
Footnotes
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Summary
Keywords
marine heatwaves, mass mortality, bioerosion, endolithic microbes, coral bleaching, phase shifts
Citation
Fordyce AJ, Ainsworth TD, Heron SF and Leggat W (2019) Marine Heatwave Hotspots in Coral Reef Environments: Physical Drivers, Ecophysiological Outcomes, and Impact Upon Structural Complexity. Front. Mar. Sci. 6:498. doi: 10.3389/fmars.2019.00498
Received
18 April 2019
Accepted
24 July 2019
Published
16 August 2019
Volume
6 - 2019
Edited by
Thomas Wernberg, The University of Western Australia, Australia
Reviewed by
Guillermo Diaz-Pulido, Griffith University, Australia; Mads Solgaard Thomsen, University of Canterbury, New Zealand; Shaun Wilson, Conservation and Attractions (DBCA), Australia
Updates
Copyright
© 2019 Fordyce, Ainsworth, Heron and Leggat.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Alexander J. Fordyce, Alexander.Fordyce@uon.edu.au
This article was submitted to Global Change and the Future Ocean, a section of the journal Frontiers in Marine Science
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