Abstract
Climatically extreme weather events often drive long-term ecological responses of ecosystems. By disrupting the important symbiosis with zooxanthellae, Marine Cold Spells (MCS) can cause bleaching and mortality in tropical and subtropical scleractinian corals. Here we report on the effects of a severe MCS on high latitude corals, where we expected to find bleaching and mortality. The MCS took place off the coast of Perth (32°S), Western Australia in 2016. Bleaching was assessed before (2014) and after (2017) the MCS from surveys of permanent plots, and with timed bleaching searches. Temperature data was recorded with in situ loggers. During the MCS temperatures dipped to the coldest recorded in ten years (15.3°C) and periods of <17°C lasted for up to 19 days. Only 4.3% of the surveyed coral colonies showed signs of bleaching. Bleaching was observed in 8 species where those most affected were Plesiastrea versipora and Montipora mollis. These findings suggest that high latitude corals in this area are tolerant of cold stress and are not persisting near a lethal temperature minimum. It has not been established whether other environmental conditions are limiting these species, and if so, what the implications are for coral performance on these reefs in a warmer future.
Introduction
Extreme weather events can cause long term ecological changes by impacting species across multiple scales from physiological performance to biogeographic distributions (e.g., Gaines and Denny, ; Hawkins et al., ). In the marine environment, extreme temperature events can be particularly detrimental with potentially wide ranging and catastrophic impacts (e.g., Southward and Burrows, ; Garrabou et al., ; Lirman et al., ; Wernberg et al., ). Both marine heatwaves (MHW's) and cold spells (MCS's) have only recently been defined in the literature (MHW's; Hobday et al., , MCS; Schlegel et al., ). However, in contrast to many recent examples of impacts of MHWs, MCS's have received much less attention (Schlegel et al., ).
Marine Cold Spells often result from upwelling and/or atmospheric forcing (Schlegel et al., ) causing temperature declines, resulting in reduced metabolic capacity and stress in warm-adapted organisms (e.g., invertebrate mortality; Gunter, ; Firth et al., , fish kills; Gunter, , ; Holt and Holt, ; Rehage et al., , coral bleaching; Roberts et al., ; Paz-García et al., ).
Temperature is a key factor determining the distribution of scleractinian corals, as they are generally warm water species confined to tropical and subtropical latitudes (Wells, ; Stehli and Wells, ; Veron, ). As seasonally cool isotherms limits the performance and distribution of many corals, this group of species can be expected to be sensitive to severely cooler conditions such as Marine Cold Spells (MCS). For tropical and subtropical scleractinian corals cold stress has been shown to impact the symbiotic relationship with zooxanthellae (Krause, ; Saxby et al., ; Hoegh-Guldberg et al., ). Under cold stress the onset of Photosystem II quenching in the zooxanthellae slows, which causes an excess of oxygen to build up in the tissue (Krause, ). Similar to warm water stress the excess oxygen can cause the formation of oxygen radicals, leading to tissue damage and the expulsion of the zooxanthellae (coral bleaching) (Saxby et al., ; Hoegh-Guldberg et al., ; Pontasch et al., ). Extreme cold stress, such as MCS, has thus been shown to be limiting for lower latitude corals and symbionts, and induce coral bleaching.
In addition to causing photosynthetic declines and disruptions to the coral–zooxanthellae symbiosis, cold stress can be lethal. Exposure to cold stress (3 −11°C below ambient) for as little as 9–12 h initially induces reduced photosynthesis and coral bleaching but beyond 12 h at severe cold stress (11°C below ambient) coral mortality can occur (Saxby et al., ). Cold spells have resulted in large scale coral bleaching on low latitude reefs such as the Great Barrier Reef (Australia, 23°S), where living coral cover plummeted from >80 to <12% (Hoegh-Guldberg et al., ). Similarly in Florida (USA, 24–27°N) coral mortality averaged 90% in some areas following cooler temperatures of 15°C (Voss, ; Davis, ; Roberts et al., ). MCS's thus have the potential to be significant drivers of stress and mortality in coral communities.
Modern coral communities in high latitude areas of Western Australia are typified by coral species with wide geographical ranges, or subtropical or temperate affinity (Greenstein and Pandolfi, ). These species are largely generalists with broad niche requirements (Sommer et al., ; Keith et al., ; Mizerek et al., ), and they regularly experience temperatures that are considered “cold” (<18°C), for these inherently tropical taxa (Veron, ). Although resilient, these corals are not impervious to the stressful conditions at high latitudes. For example high latitude conditions suppress reef building processes and limit corals to distinct communities (Kleypas et al., ). Furthermore, these populations are locally adapted, reproductively isolated and have low genetic diversity (Ayre and Hughes, ; Miller and Ayre, ; Noreen et al., ; Thomas et al., ). Similar to what has been observed in low latitude corals, cold stress, such as can be expected during unusually cold MCS, could be limiting for corals and symbionts and induce bleaching in high latitude corals.
In this study, we documented responses of high latitude corals to a severe MCS off the coast of Perth (32°S), Western Australia, where the coolest water temperatures in more than a decade, were recorded in the austral winter of 2016. As cold stress impairs metabolic processes and survival for low latitude coral reefs we expected the MCS to have caused stress in corals around Perth. As a result, we hypothesized that the high latitude coral communities would have undergone widespread bleaching and mortality from cold stress experienced during the 2016 MCS.
Methods
This study took place in Marmion Marine Park off the coast of Perth, Western Australia (Figure 1).
Figure 1
In June 2014, five permanent plots of one meter diameter (3.14 m2), were established at three offshore sites of comparable habitat and environmental conditions. The center of each plot was marked with a labeled stake for later identification. Plots were established haphazardly across the limestone reef, separated by a minimum of 10 meters at a depth of 8–12 m in areas dominated by corals, turf and fleshy seaweeds. Each plot was mapped for coral colonies, and each colony was photographed with a scale (Three Mile Reef North and South), or the whole plot was photographed as visual reference (Centaur Reef). Photographs were used for subsequent measurements of size and colony health, by comparing against a coral health chart (www.coralwatch.org) to quantify levels of bleaching. For this study, only colonies with color codes B1, C1, D1, or E1 were considered to be bleached (www.coralwatch.org). This avoided potentially assigning bleaching status to colonies with perpetual lighter pigmentation or seasonal pigment variation. Plots were surveyed in September–October 2014 prior to the marine cold spell of 2016. Survey sites were visited regularly (every ~2–3 months between 2014 and 2015, monthly 2015–2016, and ~3–4 months 2016–2017) and bleaching in >1 colony was not noted. Coral bleaching was noted anecdotally in plots in December 2016, prompting a resurvey in January 2017 (austral summer). Summer temperatures prior to the surveys were comparable to regularly recorded high temperatures (December average 2006-15 = 21.4°C (max 24.0°C) vs. December average 2016 = 21.7°C (max 24.0°C); Wernberg unpublished data) and unlikely to have been the source of bleaching. Overgrowth by turf algae on all bleached colonies further indicated that the bleaching had not occurred more recently in December 2016, immediately prior to the re-surveys. Due to loss of labeled stakes three plots were surveyed from Three Mile Reef North, four from Three Mile Reef South and four from Centaur Reef in 2017. In addition to the permanent plots, timed searches for additional coral bleaching was also undertaken in January and February 2017, at all three sites as well as at an additional three inshore sites (Figure 1). All colonies encountered in the 30 min searches were photographed for subsequent measurements of size and colony health (as above).
Chi-square goodness of fit tests were used to determine if the proportion of bleached colonies was significantly different between species, and between inshore and offshore reefs.
Temperature was recorded in situ every hour by an Onset Tidbit logger attached to a stake ~5 cm above the reef surface at Centaur Reef (Figure 1). See Smale and Wernberg () for additional information.
Results
During 2016 temperatures in Marmion dipped to 15.3°C, the coldest temperature recorded in >10 years. Anomalously cold temperatures occurred in nine months of the year, based on ten year average monthly temperatures, and a continuous period of <17°C (below any long term monthly average) occurred for ~19 days during August–September (Figure 2). In the months prior to bleaching being noted in December 2016, other temperature anomalies (e.g., heat spikes) were not seen (Figure 2).
Figure 2
A total of 244 coral colonies were found and re-surveyed in the nine permanent plots after the marine cold spell (Figure 3) and the number of colonies increased in total due to an increased number of small corals (<1 cm) (Table 1). The number of bleached colonies increased from zero before to ten (4.3%) after the MCS, and of the ten bleached corals four were > 50% bleached and six <50% bleached (Figure 4A). The bleached colonies occurred at all sites and were found in six of the nine plots. Bleaching was found in two of the ten species recorded within the plots. Montipora mollis had slightly more bleached colonies than Plesiastrea versipora (Figure 4B). Of the 234 healthy colonies the majority were P. versipora and Paragoniastrea australensis (Figure 4C). A large majority of the healthy colonies were also recruits so the highest taxonomic identification they could be assigned was family (Merulinidae).
Figure 3
Table 1
| Species | Life Stage | 2014 | 2016 |
|---|---|---|---|
| Turbinaria reniformis | Adult | 2 | 2 |
| Montipora mollis | Adult | 5 | 5 |
| Favites abdita | Adult | 1 | 1 |
| Dipastrea favus | Adult | 2 | 2 |
| Coscinaraea mcneilli | Adult | 1 | 1 |
| Pocillopora damicornis | Adult | 1 | 1 |
| Turbinaria mesenterina | Adult | 1 | 1 |
| Plesiastrea versipora | Adult | 9 | 11 |
| Recruit | 19 | 24 | |
| Coelastrea aspera | Adult | 7 | 11 |
| Recruit | 0 | 3 | |
| Paragoniastrea australensis | Adult | 8 | 21 |
| Recruit | 0 | 1 | |
| Total | 56 | 84 |
Relative abundances of species at different life stages before (2014) and after (2016) the Marine Cold Spell in permanent plots within Marmion Marine Park.
Abundances are from Three Mile Reef North and South only where plots where mapped for individual colonies, and recruits refer to colonies with a diameter ≤ 1 cm.
Figure 4
Timed searches revealed an additional eight species had undergone bleaching than was found in the permanent plots. In addition to more P. versipora and M. mollis, we found bleached colonies of P. australensis, Turbinaria reniformis, Coelastrea aspera, Dipastrea favus, Turbinaria mesenterina, and Pocillopora damicornis (Table 2). The frequency of bleaching was significantly different between species (Chi-square test p < 0.05) and the frequency of bleaching in the eight effected species was not independent of shelf position (inshore vs. offshore, Chi-square test p < 0.05). This was likely the result of the large proportion of bleached M. mollis on offshore reefs and only bleached M. mollis and P. versipora being common to both inshore and offshore reefs (Table 2).
Table 2
| Species | Offshore | Inshore | |||
|---|---|---|---|---|---|
| N | Percent (%) | N | Percent (%) | Total | |
| Montipora mollis | 17 | 42.5 | 6 | 15.0 | 23 |
| Paragoniastrea australensis | 2 | 5.0 | 0 | 0.0 | 2 |
| Plesiastrea versipora | 2 | 5.0 | 2 | 5.0 | 4 |
| Turbinaria reniformis | 1 | 2.5 | 0 | 0.0 | 1 |
| Coelastrea aspera | 0 | 0.0 | 2 | 5.0 | 2 |
| Dipastrea favus | 0 | 0.0 | 1 | 2.5 | 1 |
| Pocillopora damicornis | 0 | 0.0 | 3 | 7.5 | 3 |
| Turbinaria mesenterina | 0 | 0.0 | 4 | 10.0 | 4 |
| Total | 22 | 55.0 | 18 | 45.0 | 40 |
Species found with coral bleaching after the Marine Cold Spell on inshore and offshore reefs of Marmion Marine Park, Perth, Western Australia in timed searches.
N = total count of bleached colonies per species, percent = percentage each species contributed to the total bleaching pool.
Discussion
In this study we found corals in Marmion Marine Park (32°S) to be largely unaffected by a severe marine cold spell. Our hypothesis, that corals would undergo bleaching and mortality was documented but not extensively. We had expected the unusually low temperature anomalies and duration of the MCS would have induced physiological stress, leading to a disruption in the coral-zooxanthellae symbiosis and to coral bleaching. However, this only occurred for a small number of corals and was not widespread across the coral community. The coastal area adjacent to Marmion Marine Park did not receive unusually high solar exposure between October–December 2016 compared to previous years (www.bom.gov.au) nor were other temperature anomalies seen in late 2016, ruling out warm water or light induced bleaching. This suggests that the symbiotic relationship between zooxanthellae and high latitude corals is not particularly stressed by anomalously cold temperatures, and that these corals are not persisting near their lethal temperature minima.
High latitude areas are challenging environments for inherently tropical taxa such as scleractinian corals. Low temperatures, low light availability and high attenuation in winter, low aragonite saturation and high competition with seaweeds are pervasive stressors for corals in these environments (Miller, ; Miller and Hay, ; Kleypas et al., ; Sommer et al., ). These stressors filter species so that high latitude coral communities are largely dominated by corals which are generalists with broad niche requirements (Sommer et al., ; Keith et al., ; Mizerek et al., ). The stress tolerant nature of most high latitude species could thus explain the low impact of the 2016 MCS.
It has been shown that low temperatures do not necessarily have detrimental impacts for corals and symbionts. Prolonged exposure to cold stress (−5°C below ambient) in aquaria has shown corals to acclimate and recover after initial declines in health and mild bleaching (Roth et al., ; Roth and Deheyn, ). One mechanisms enabling tolerance to cold stress, particularly when energy transfer from zooxanthellae to coral is absent or drastically reduced, is supplementing with heterotrophic feeding (Miller, ; Leletkin, ; Howe and Marshall, ; Anthony and Connolly, ; Grottoli et al., ; Houlbrèque and Ferrier-Pagès, ; Levas et al., ). Corals also maintain energy reserves (as lipids), which are utilized by some species to aid recovery after bleaching (Rodrigues and Grottoli, ). Thus mechanisms for energy acquisition may play an important role in managing stress to low temperatures such as those experienced during the 2016 MCS.
Although high latitude corals tolerate low temperatures these conditions often have sub lethal impacts. In broad terms, temperatures which regularly drop below 18°C for extended periods of time (weeks to months; Veron, ) are considered cold for corals as they limit reef building processes. In some areas of southern Australia, for example, temperatures can dip to 12°C (Petrusevics, ), however this is at the cost of growth which ranges from 1.5–7.8 mm year−1 (Burgess et al., ). The 2016 MCS likely had similar sub lethal impacts and we expect that these corals would have depressed growth and possibly additional trade-offs such as reduced reproductive fitness.
It is clear that the 2016 MCS had little impact on high latitude corals in this study. This suggests that high latitude corals are not particularly limited by low temperatures, and other factors (potentially light, aragonite saturation and competition with seaweeds; Miller, ; Miller and Hay, ; Kleypas et al., ; Sommer et al., ) play a significant role. Therefore under a warmer future, temperature increase alone, may not make high latitudes any more suitable for coral performance than current conditions. However temperature increases have already indirectly alleviated competition with seaweeds at high latitude (Vergés et al., ; Tuckett et al., ), and its role in mitigating other limiting factors (e.g., light) has been proposed (Sommer et al., ). It has not been established if other environmental conditions are limiting these species, and if so, what the implications are for coral performance on these reefs in a warmer future.
Statements
Author contributions
CT and TW designed the study; CT and TW collected data; CT identified corals, performed data analysis and led the writing; both authors contributed to the final version.
Funding
This study was funded by grants to TW from the Australian Research Council (DP170100023) and the Hermon Slade Foundation (HSF13/13).
Acknowledgments
We thank E. Thomas, Y. Mulders, S. Straub, and M. Moustaka for assistance in the field.
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 AWL and handling Editor declared their shared affiliation.
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Summary
Keywords
Marine cold spell (MCS), coral bleaching, Plesiastrea versipora, Montipora mollis, stress-tolerant species
Citation
Tuckett CA and Wernberg T (2018) High Latitude Corals Tolerate Severe Cold Spell. Front. Mar. Sci. 5:14. doi: 10.3389/fmars.2018.00014
Received
31 July 2017
Accepted
16 January 2018
Published
31 January 2018
Volume
5 - 2018
Edited by
Emma Camp, University of Technology Sydney, Australia
Reviewed by
Anthony William Larkum, University of Technology Sydney, Australia; Aldo Cróquer, Simón Bolívar University, Venezuela
Updates
Copyright
© 2018 Tuckett and Wernberg.
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 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: Chenae A. Tuckett chenae.tuckett@research.uwa.edu.au
This article was submitted to Coral Reef Research, a section of the journal Frontiers in Marine Science
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