Sensitivity of calcification to thermal stress varies among genera of massive reef-building corals

Reductions in calcification in reef-building corals occur when thermal conditions are suboptimal, but it is unclear how they vary between genera in response to the same thermal stress event. Using densitometry techniques, we investigate reductions in the calcification rate of massive Porites spp. from the Great Barrier Reef (GBR), and P. astreoides, Montastraea faveolata, and M. franksi from the Mesoamerican Barrier Reef (MBR), and correlate them to thermal stress associated with ocean warming. Results show that Porites spp. are more sensitive to increasing temperature than Montastraea, with calcification rates decreasing by 0.40 g cm(-2) year(-1) in Porites spp. and 0.12 g cm(-2) year(-1) in Montastraea spp. for each 1°C increase. Under similar warming trends, the predicted calcification rates at 2100 are close to zero in Porites spp. and reduced by 40% in Montastraea spp. However, these predictions do not account for ocean acidification. Although yearly mean aragonite saturation (Ω(ar)) at MBR sites has recently decreased, only P. astreoides at Chinchorro showed a reduction in calcification. In corals at the other sites calcification did not change, indicating there was no widespread effect of Ω(ar) changes on coral calcification rate in the MBR. Even in the absence of ocean acidification, differential reductions in calcification between Porites spp. and Montastraea spp. associated with warming might be expected to have significant ecological repercussions. For instance, Porites spp. invest increased calcification in extension, and under warming scenarios it may reduce their ability to compete for space. As a consequence, shifts in taxonomic composition would be expected in Indo-Pacific reefs with uncertain repercussions for biodiversity. By contrast, Montastraea spp. use their increased calcification resources to construct denser skeletons. Reductions in calcification would therefore make them more susceptible to both physical and biological breakdown, seriously affecting ecosystem function in Atlantic reefs.     

Resolving the interactions of ocean acidification and temperature on coral calcification media pH

Coral Reefs - Ocean acidification typically reduces the calcification rates of massive Porites spp. corals, but increasing seawater temperatures (below the stress and bleaching threshold) can...     

Sea surface temperature and the growth of the West Atlantic reef-building coral Montastraea annularis

Relationships were analyzed between sea surface temperature (SST) and annual growth characteristics (density, extension rate and calcification rate) of the Caribbean reef-building coral Montastraea annularis. Colonies were collected from 12 localities in the Gulf of Mexico and the Caribbean Sea. Two well-separated relationships were found, one for the Gulf of Mexico and the other for the Caribbean Sea. Calcification rate and skeletal density increased with increasing SST in both regions, while extension rate tended to decrease. Calcification rate increased ∼0.57 g cm⁻² year⁻¹ for each 1 °C increase in SST. Zero calcification was projected to occur at 23.7 °C in corals from the Gulf of Mexico and at 25.5 °C in corals from the Caribbean Sea. The 24 °C annual average SST isotherm marks the northern limit of distribution of M. annularis. Montastraea annularis populations of the Gulf of Mexico are isolated from those of the Caribbean Sea, and results indicate that corals from the Gulf of Mexico are adapted to growth at lower minimum and average annual SST. Corals from both the Gulf of Mexico and the Caribbean Sea, growing at lower SSTs and having lower calcification rates, extend their skeletons the same or more than those growing at higher SSTs. They achieve this by putting more of their calcification resources into extension and less into thickening, i.e., by sacrificing density.     

Reef location has a greater impact than coral bleaching severity on the microbiome of Pocillopora acuta

Coral Reefs - Coral reefs are increasingly threatened by heat stress events leading to coral bleaching. In 2016, a mass bleaching event affected large parts of the Great Barrier Reef (GBR). Whilst...     

Declining coral calcification in massive Porites in two nearshore regions of the northern Great Barrier Reef

Temporal and spatial variation in the growth parameters skeletal density, linear extension and calcification rate in massive Porites from two nearshore regions of the northern Great Barrier Reef (GBR) were examined over a 16‐year study period. Calcification rates in massive Porites have declined by approximately 21% in two regions on the GBR ～450 km apart. This is a function primarily of a decrease in linear extension (～16%) with a smaller decline in skeletal density (～6%) and contrasts with previous studies on the environmental controls on growth of massive Porites on the GBR. Changes in the growth parameters were linear over time. Averaged across colonies, skeletal density declined over time from 1.32 g cm^?3 (SE = 0.017) in 1988 to 1.25 g cm^?3 (0.013) in 2003, equivalent to 0.36% yr^?1 (0.13). Annual extension declined from 1.52 cm yr^?1 (0.035) to 1.28 cm yr^?1 (0.026), equivalent to 1.02% yr^?1 (0.39). Calcification rates (the product of skeletal density and annual extension) declined from 1.96 g cm^?2 yr^?1 (0.049) to 1.59 g cm^?2 yr^?1 (0.041), equivalent to 1.29% yr^?1 (0.30). Mean annual seawater temperatures had no effect on skeletal density, but a modal effect on annual extension and calcification with maxima at ～26.7 °C. There were minor differences in the growth parameters between regions. A decline in coral calcification of this magnitude with increasing seawater temperatures is unprecedented in recent centuries based on analysis of growth records from long cores of massive Porites. We discuss the decline in calcification within the context of known environmental controls on coral growth. Although our findings are consistent with studies of the synergistic effect of elevated seawater temperatures and pCO₂ on coral calcification, we conclude that further data on seawater chemistry of the GBR are required to better understand the links between environmental change and effects on coral growth.     

琼东海域橙黄滨珊瑚骨骼生长特性及其主要影响因素

基于珊瑚骨骼X射线照片,使用CoralXDS软件,对海南岛(琼)东部海域的橙黄滨珊瑚生长特性进行研究,获取了百年来的年生长率(ER)、骨骼密度(D)和钙化速率(CR) 3种生长参数.结果表明: 该橙黄滨珊瑚ER的变化范围为0.49～1.10 cm·a^-1,年均值0.76 cm·a^-1;D的变化范围1.11～1.35 g·cm^-3,年均值1.22 g·cm^-3;CR的变化范围为0.55～1.41 g·cm^-2·a^-1,年均值0.94 g·cm^-2·a^-1.统计分析表明,研究海区表层水温(SST)是橙黄滨珊瑚骨骼生长参数变化的主要环境影响因素,对ER和CR的控制较强,对D的影响较弱,但总体上3项生长参数都随SST升高而增大.光照、盐度和水动力条件等是次要影响因素.台风和强热带风暴对琼东海域橙黄滨珊瑚骨骼密度条带分布的影响也较为显著.复杂的气候环境,赋予了橙黄滨珊瑚骨骼多变的生长模式.过去一个世纪以来,琼东海域年平均表层水温显著上升,气候倾向率为0.15 ℃·(10 a)^-1,SST上升分为两个阶段,20世纪40年代初和80年代初,人类活动加剧和全球气候变暖是导致琼东海域SST显著上升的原因.     

Heat stress differentially impacts key calcification mechanisms in reef-building corals

Coral Reefs - Coral reefs are increasingly threatened by climate change, mass bleaching events and ocean acidification (OA). Coral calcification, a process that is critical to build and maintain...     

Seasonal calcification of the coral Acropora digitifera from a subtropical marginal Okinawa reef under ocean acidification

Coral Reefs - Coral calcification is affected by the decrease in aragonite saturation state (Ωarag) caused by ocean acidification (OA). However, OA effects are modulated by other environmental...     

Porites growth characteristics in a changed environment: Misima Island, Papua New Guinea

 The construction in 1988 of an open-cut gold mine and ore-processing facility at Misima Island, Papua New Guinea, resulted in disturbance of the adjacent fringing coral reef, mostly because of large increases in sedimentation. This provided an opportunity to examine whether growth characteristics of the major reef-building coral, Porites, changed in response to this sudden and sustained increase in sedimentation. Annual variation in skeletal density was measured in 93 colonies variously affected by sedimentation. The colonies provided data for average annual density, annual extension and annual calcification covering the periods 5 y before and 5 y after mining operations began. The average depth of skeleton occupied by tissue (tissue layer thickness) was also measured for most colonies. There was high mortality of Porites in regions strongly affected by increased sedimentation. In colonies that survived, density, extension and calcification tended to be less (in some cases significantly) in the period after mining operations began compared with pre-construction levels. However, these decreases were not linked with proximity to the mine site and probably reflect a regional-scale response of Porites growth to some other environmental change. This suggests that periods of high sedimentation may not be recorded by the growth characteristics of massive Porites. Average growth characteristics of surviving Porites from Misima Island were similar to those from inshore reefs of the northern Great Barrier Reef (GBR). Tissue layer thickness in Porites from the control areas at Misima Island were also similar to colonies from the northern inshore GBR reefs. However, tissue layer thickness significantly decreased with increased proximity to the mine site at Misima Island. Accepted: 15 May 1999     

Evaluating climate indices and their geochemical proxies measured in corals

Coral Reefs -  Standard ocean/climate indices such as the Niño-3 sea surface temperature (SST) index, based on sparse instrumental data, and atmospheric indices such as the Southern...     

Incorporating benthic community changes into hydrochemical-based projections of coral reef calcium carbonate production under ocean acidification

Coral Reefs - The existence of coral reefs is dependent on the production and maintenance of calcium carbonate (CaCO3) framework that is produced through calcification. The net production of CaCO3...     

Shell formation in the giant clam,Tridacna squamosa,may involve an apical Na+/Ca2+ exchanger 3 homolog in the shell-facing epithelium of the whitish inner mantle,which displays light-enhanced gene and protein expression

Coral Reefs - Na+/Ca2+ exchangers (NCXs) transport one Ca2+ in exchange for three Na+ and may participate in the calcification processes of mammalian osteoblasts and invertebrate calcifying cells....     

Assessing loss of coral cover on the Great Barrier Reef: A response to Hughes et al. (2011)

Hughes et al. (Coral Reefs, 2011, in press) challenge our interpretations of the changes in coral cover observed on the Great Barrier Reef (GBR) between 1986 and 2004 (Sweatman et al. in Coral Reefs 30:521–531, 2011). They question whether we can accurately assign all causes of coral loss; we contend that this makes no difference to the observed changes. They defend the validity of historical data on coral cover from before the start of systematic large-scale monitoring and conclude that coral cover has been declining since at least 1960, but we find no trend in the early data. We remain convinced that combining data collected at different spatial scales (quadrats and transects in the past mixed with more recent whole-reef averages from manta tows) are likely to overestimate decline, because whole-reef averages will very rarely reach the high cover values that can occur at the quadrat scale. Hughes et al. (Coral Reefs, 2011, in press) state that we dismiss runoff as a cause of ecosystem degradation; we defend our interpretations and dispute some of their examples. In summary, we stand by our conclusion that coral cover on the GBR declined in the period 1986–2004 but through localised and unsynchronised changes that included recovery.     

Regional decline in growth rates of massive Porites corals in Southeast Asia

This study reports the first well‐replicated analysis of continuous coral growth records from warmer water reefs (mean annual sea surface temperatures (SST) >28.5 °C) around the Thai–Malay Peninsula in Southeast Asia. Based on analyses of 70 colonies sampled from 15 reefs within six locations, region‐wide declines in coral calcification rate (ca. 18.6%), linear extension rate (ca. 15.4%) and skeletal bulk density (ca. 3.9%) were observed over a 31‐year period from 1980 to 2010. Decreases in calcification and linear extension rates were observed at five of the six locations and ranged from ca. 17.2–21.6% and ca. 11.4–19.6%, respectively, whereas decline in skeletal bulk density was a consequence of significant reductions at only two locations (ca. 6.9% and 10.7%). A significant link between region‐wide growth rates and average annual SST was found, and Porites spp. demonstrated a high thermal threshold of ca. 29.4 °C before calcification rates declined. Responses at individual locations within the region were more variable with links between SST and calcification rates being significant at only four locations. Rates of sea temperature warming at locations in the Andaman Sea (Indian Ocean) (ca. 1.3 °C per decade) were almost twice those in the South China Sea (Pacific Ocean) (ca. 0.7 °C per decade), but this was not reflected in the magnitude of calcification declines at corresponding locations. Considering that massive Porites spp. are major reef builders around Southeast Asia, this region‐wide growth decline is a cause for concern for future reef accretion rates and resilience. However, this study suggests that the future rates and patterns of change within the region are unlikely to be uniform or dependent solely on the rates of change in the thermal environment.     

The impact of seawater temperature on coral growth parameters of the colonial coral Cladocora caespitosa (Anthozoa, Scleractinia) in the eastern Adriatic Sea

The scleractinian coral Cladocora caespitosa deserves a special place among the major carbonate bioconstructors of the Mediterranean Sea. Annual coral skeleton growth, coral calcification, and skeleton density of the colonial coral C. caespitosa taken from 25 locations in the eastern Adriatic Sea were analyzed and compared with annual sea surface temperatures (SST). The growth rates of the coral C. caespitosa from the 25 stations in the Adriatic Sea ranged from 1.92 to 4.19?mm per year, with higher growth rates of the investigated corallites in the southern part of the Adriatic Sea. These growth rates are similar to those measured in other areas of the Mediterranean Sea. The correlation between coral growth and sea temperatures in the Adriatic Sea is seen as follows: An X-radiograph analysis of coral growth in C. caespitosa colonies that are over 60?years old showed that higher growth rates of this coral coincided with a warmer period in the Mediterranean Sea. A positive significant correlation exists between corallite growth rates and SST and coral calcification and SST. A negative correlation exists between coral density and SST. Coral growth rates also showed a correlation with higher eutrophication caused by nearby fish farms, along with a greater depth of the investigated colonies and high bottom currents.     

Reproductive cycle and trophic ecology in deep versus shallow populations of the Mediterranean gorgonian Eunicella singularis (Cap de Creus,northwestern Mediterranean Sea)

Coral Reefs - The annual gonad development of a shallow (20 m depth) population of the Mediterranean gorgonian Eunicella singularis was found to be closely synchronized with that of a deep...     

Shifting base-lines, declining coral cover, and the erosion of reef resilience: comment on Sweatman et al. (2011)

Formal monitoring of the Great Barrier Reef was initiated in 1986 in response to the clear scientific evidence (and growing public concern) over the loss of corals caused by two protracted outbreaks of crown-of thorns starfish, which began in 1962 and 1979. Using monitoring data from manta tows along and across the Great Barrier Reef, Sweatman et al. (Coral Reefs 30:521–531, 2011) show that coral cover after these outbreaks declined further from 28 to 22% between 1986 and 2004. Pointing to the current levels of protection of the Great Barrier Reef, they state that earlier estimates of losses of coral cover since the early 1960s have been exaggerated. However, the loss of close to one-quarter of the coral cover over the past two decades represents an average loss of 0.34% cover per year across the whole GBR after 1986, which is very similar to previously reported rates of annual loss measured over a longer timeframe. The heaviest recent losses have occurred on inshore and mid-shelf reefs, which Sweatman et al. (Coral Reefs 30:521–531, 2011) attribute to a natural cycle of disturbance and recovery. But there has been very limited recovery. While coral cover has increased for short periods on some individual reefs, it has declined sharply on many more to produce the observed system-wide trend of declining cover. Close to 40% of coral cover on inner reefs has been lost since 1986. Of particular significance is the new evidence that coral cover has remained unchanged or declined further from a low 1986 baseline in 28 out of 29 sub-regions of the Great Barrier Reef, indicating a gradual erosion of resilience that is impeding the capacity of this huge reef system to return towards its earlier condition. This result, and other clear evidence of widespread incremental degradation from overfishing, pollution, and climate change, calls for action rather than complacency or denial.     

Ecological consequences of Stony Coral Tissue Loss Disease in the Turks and Caicos Islands

Coral Reefs - Coral reefs are suffering global declines due to climate change, natural disasters, pollution, and diseases. Coral disease events have increased in frequency and severity in the past...     

Distribution of Acanthaster planci at Lord Howe Island,the southern-most Indo-Pacific reef

Lord Howe Island, at 31°33S, supports the southern-most coral reef in the Indo-Pacific region, located approximately 150 and 200 km south of Elizabeth and Middleton Reefs and 1000 km south of the Great Barrier Reef (GBR). Systematic SCUBA searches in 1987 indicated that Acanthaster planci was present at 3 of 10 sites surveyed, at densities of up to 5 individuals ha^-1. Further surveys in 1989 indicated that the population was increasing, with densities of 20–46 ha^-1 recorded from 7 of 13 sites. The size structures of the 1987 and 1989 populations were suggestive of annual recruitment since 1985. Individuals larger than 25 cm diameter were gravid during both surveys, raising the possibility that the population may be self-seeding. Alternatively, the population may be maintained by larvae dispersed in the East Australian Current from the southern GBR or in eddies from Elizabeth and Middleton Reefs. This study provides the first records for distribution of 7 species of scleractinian coral at Lord Howe Is. Reef.