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.     

Gender-related differences in the apparent timing of skeletal density bands in the reef-building coral Siderastrea siderea

Density banding in skeletons of reef-building corals is a valuable source of proxy environmental data. However, skeletal growth strategy has a significant impact on the apparent timing of density-band formation. Some corals employ a strategy where the tissue occupies previously formed skeleton during as the new band forms, which leads to differences between the actual and apparent band timing. To investigate this effect, we collected cores from female and male colonies of Siderastrea siderea and report tissue thicknesses and density-related growth parameters over a 17-yr interval. Correlating these results with monthly sea surface temperature (SST) shows that maximum skeletal density in the female coincides with low winter SSTs, whereas in the male, it coincides with high summer SSTs. Furthermore, maximum skeletal densities in the female coincide with peak Sr/Ca values, whereas in the male, they coincide with low Sr/Ca values. Both results indicate a 6-month difference in the apparent timing of density-band formation between genders. Examination of skeletal extension rates also show that the male has thicker tissue and extends faster, whereas the female has thinner tissue and a denser skeleton—but both calcify at the same rate. The correlation between extension and calcification, combined with the fact that density banding arises from thickening of the skeleton throughout the depth reached by the tissue layer, implies that S. siderea has the same growth strategy as massive Porites, investing its calcification resources into linear extension. In addition, differences in tissue thicknesses suggest that females offset the greater energy requirements of gamete production by generating less tissue, resulting in differences in the apparent timing of density-band formation. Such gender-related offsets may be common in other corals and require that environmental reconstructions be made from sexed colonies and that, in fossil corals where sex cannot be determined, reconstructions must be duplicated in different colonies.     

Experimental responses to elevated water temperature in genotypes of the reef coral<Emphasis Type="Italic"> Pocillopora damicornis</Emphasis> from upwelling and non-upwelling environments in Panama

The authors investigated the response to experimentally elevated water temperature in genotypes of Pocillopora damicornis from three coral reefs in the upwelling Gulf of Panama and four coral reefs in the non-upwelling Gulf of Chiriquí, Panamanian Pacific. Sea-surface temperature in the Gulf of Panama declines below 20 °C during seasonal upwelling, while in the thermally stable Gulf of Chiriquí, the temperature ranges from 27 to 29 °C. Genotypes of P. damicornis from the seven locations were determined by allozyme electrophoresis. The most abundant genotype at each location was selected for a thermal tolerance experiment where corals were exposed to water temperature of 30 °C (1 °C above ambient) for 43 days. Four site coral genotypes can be uniquely differentiated by the GPI locus, two by the LGG-2 locus, and two by a combination of the MDH-1, LGG-2, and LTY-3 loci. A visual assessment of the coral condition after exposure to an elevated temperature showed that corals from localities in the non-upwelling environment retained a normal to slightly pale appearance, while corals from the upwelling environment bleached and their polyps were mostly retracted. A two-way ANOVA confirmed that corals were significantly affected by water temperature and locality. The zooxanthellae were also significantly affected by the interaction of elevated temperature and locality of the corals. Mean zooxanthellae density decreased by 25 and 55%, respectively, in experimentally heated corals from the non-upwelling and upwelling environments. Low concentrations of photosynthetic pigments per live area of the corals were the norm in corals under elevated temperature. The mean concentration of chlorophyll a per live area of the corals was reduced by 17 and 49%, respectively, in heated corals from the non-upwelling and upwelling sites. Coral genotypes from the upwelling Gulf of Panama demonstrated higher vulnerability to thermal stress than coral genotypes from the non-upwelling Gulf of Chiriquí. However, the latter showed greater differences in their responses. Thus, even at small geographic scales, corals can display different levels of tolerance to thermal stress. The difference in thermal tolerance between corals from upwelling and non-upwelling environments is concomitant with greater genetic differences in experimental corals from the thermally stable Gulf of Chiriquí compared with corals from the upwelling Gulf of Panama.Communicated by K.S. Sealey     

Temperature effects on calcification rate and skeletal deposition in the temperate coral, Plesiastrea versipora (Lamarck)

The geographic range of the coral, Plesiastrea versipora (Lamarck, 1816), extends into temperate waters outside the southern limit for hermatypic corals. In the present study, calcification in Plesiastrea collected from Port Phillip Bay, Victoria was examined over the coral's normal annual temperature range (10-21 °C), which is well below the normal optimum for coral calcification in tropical corals (25-28 °C). Calcification rate in Plesiastrea was considerably lower than in reef corals, but showed a similar pattern in temperature responses, with a trend towards higher rates at ∼18 °C. The light/dark calcification ratio was markedly lower than that in tropical corals. Autoradiography showed that calcification occurred primarily by deposition of calcium carbonate at the upper surfaces of the septo-costae. Scanning electron microscopy (SEM) showed that skeletal deposition in Plesiastrea had a temperature-dependent diel pattern. In the light, calcium carbonate was deposited as small spheroidal crystals and, at higher temperatures, small needle-shaped crystals. In the dark, calcium carbonate deposition appeared to be in the form of an amorphous sheet-like cementation. Compared with other scleractinian corals, calcification rate in Plesiastrea was relatively slow and showed different patterns of skeletal deposition.     

Effect of zooplankton availability on the rates of photosynthesis, and tissue and skeletal growth in the scleractinian coral Stylophora pistillata

This work investigated the effect of light and feeding on tissue composition as well as on rates of photosynthesis and calcification in the zooxanthellae (zoox) scleractinian coral, Stylophora pistillata. Microcolonies were maintained at three different light levels (80, 200, 300 μmol m⁻² s⁻¹) and subjected to two feeding regimes (starved and fed) over 9 weeks. Corals were fed both natural plankton and Artemia salina nauplii four times a weeks and samplings were made after 2, 5, and 9 weeks. Results confirmed that feeding enhances coral growth rate and increases both the dark and light calcification rates. These rates were 50-75% higher in fed corals (FC; 60±20 and 200±40 nmol Ca²⁺ cm⁻² h⁻¹ for dark and light calcification, respectively) compared to control corals (CC; 30±9 and 124±23 nmol Ca²⁺ cm⁻² h⁻¹). The dark calcification rates, however, were four times lower than the rates of light calcification (independent of trophic status). After 5 weeks, chlorophyll a (chl-a) concentrations were four to seven times higher in fed corals (7-21 μg cm⁻²) than in control corals (2-5 μg cm⁻²). The amount of protein was also significantly higher in fed corals (2.11-2.50 mg cm⁻²) than in control corals (1.08-1.52 mg cm⁻²). Rates of photosynthesis in fed corals were 2-10 times higher (1.24±0.75 μmol O₂ h⁻¹ cm⁻²) than those measured in control corals (0.20±0.08 μmol O₂ h⁻¹ cm⁻²).     

Fine-Scale Skeletal Banding Can Distinguish Symbiotic from Asymbiotic Species among Modern and Fossil Scleractinian Corals

Understanding the evolution of scleractinian corals on geological timescales is key to predict how modern reef ecosystems will react to changing environmental conditions in the future. Important to such efforts has been the development of several skeleton-based criteria to distinguish between the two major ecological groups of scleractinians: zooxanthellates, which live in symbiosis with dinoflagellate algae, and azooxanthellates, which lack endosymbiotic dinoflagellates. Existing criteria are based on overall skeletal morphology and bio/geo-chemical indicators—none of them being particularly robust. Here we explore another skeletal feature, namely fine-scale growth banding, which differs between these two groups of corals. Using various ultra-structural imaging techniques (e.g., TEM, SEM, and NanoSIMS) we have characterized skeletal growth increments, composed of doublets of optically light and dark bands, in a broad selection of extant symbiotic and asymbiotic corals. Skeletons of zooxanthellate corals are characterized by regular growth banding, whereas in skeletons of azooxanthellate corals the growth banding is irregular. Importantly, the regularity of growth bands can be easily quantified with a coefficient of variation obtained by measuring bandwidths on SEM images of polished and etched skeletal surfaces of septa and/or walls. We find that this coefficient of variation (lower values indicate higher regularity) ranges from ~40 to ~90% in azooxanthellate corals and from ~5 to ~15% in symbiotic species. With more than 90% (28 out of 31) of the studied corals conforming to this microstructural criterion, it represents an easy and robust method to discriminate between zooxanthellate and azooxanthellate corals. This microstructural criterion has been applied to the exceptionally preserved skeleton of the Triassic (Norian, ca. 215 Ma) scleractinian Volzeia sp., which contains the first example of regular, fine-scale banding of thickening deposits in a fossil coral of this age. The regularity of its growth banding strongly suggests that the coral was symbiotic with zooxanthellates.     

CLASSIFICATION AND CONTROLS OF INTERNAL BANDING IN PALAEOZOIC STROMATOPOROIDS AND COLONIAL CORALS

Abstract:  Palaeozoic corals and stromatoporoids exhibit a variety of internal banding phenomena, many of which have been commonly interpreted as annual growth bands. We evaluate bands through analysis of colonial corals and stromatoporoids from three stratigraphic intervals: Upper Ordovician of Manitoba Canada, and Llandovery–Wenlock and Ludlow of Gotland, Sweden. Banding features are divided into four categories: (1) absence of banding; (2) density banding formed by variation in density or form of elements; (3) growth-interruption banding indicating growth cessation and regeneration; and (4) post-mortem banding caused by compaction or diagenesis. For discrimination of band types, it is essential to examine internal structures and skeletal margins in thin sections or acetate peels. Species vary considerably in degree and type of banding; each has a distinct pattern of variation. We propose criteria to determine if banding is consistent with seasonally induced growth variation: (1) consistency in band character and thickness; (2) continuity of skeletal growth; (3) marginal features; and (4) evidence of diagenetic alteration. Density bands in tabulate and rugose corals probably represent annual growth variations, but results for stromatoporoids are more ambiguous; although stromatoporoids commonly show banding, unequivocal density banding is poorly developed and growth interruption generated most stromatoporoid banding. Cerioid rugose and tabulate corals possess the thickest density bands; the thinnest bands are in stromatoporoids and heliolitid tabulates.     

The biology and physiology of alga-invertebrate symbioses. III. In situ measurements of photosynthesis and calcification in some hermatypic corals

In situ measurements of the rates of photosynthesis and calcification in three species of hermatypic corals were made at Eilat, in the Gulf of Aqaba, Red Sea. Experiments were made at 5, 20 and 35 m depth under unusually poor conditions of submarine illumination for the region, and at the relatively low water temperature (21°C) for coral growth which prevails there all year. Estimates of photosynthetic rates by both the ¹⁴C and oxygen methods indicated that the ¹⁴C method does measure gross photosynthesis in these organisms even at, and below, light compensation points. Substantial rates of carbon fixation in Acropora and Millepora show that, even under bad conditions, these organisms could survive autotrophically to at least 10 m depth, as also could the massive coral Goniastrea although this had much lower photosynthetic rates under the same conditions, compensated for by a much lower respiratory rate than the other two corals.Calcification rates were variable but showed a considerable increase in light as compared with the dark in all three species, and the rates did not decrease with depth as much as might have been anticipated from the reduction in photosynthesis and ambient light energy. Photosynthetic and calcification rates were similar to those reported for similar organisms both in the Caribbean and on the Great Barrier Reef.     

Inferred calcification rate of a temperate azooxanthellate caryophylliid coral along a wide latitudinal gradient

Correlations between environmental parameters (depth temperature and solar radiation) and growth parameters (bulk skeletal density, linear extension rate and net calcification rate) of the solitary azooxanthellate coral, Caryophyllia inornata, were investigated along an 8° latitudinal gradient on the western Italian coasts. Net calcification rate correlated positively with both bulk skeletal density and linear extension rate, showing that C. inornata allocates calcification resources evenly to thickening the skeleton and increasing linear growth. Overall, the three growth parameters did not follow gradients in the two environmental parameters, showing a different trend compared to most studies on zooxanthellate corals. However, the results are in agreement with the only previous analysis of an azooxanthellate coral, Leptopsammia pruvoti, studied along the same latitudinal gradient. In a comparison of the response to temperature of all Mediterranean species whose growth has been investigated to date, azooxanthellate corals were more tolerant to temperature increases than zooxanthellate corals.     

Coral growth rates and environmental control of density banding

Linear and mass growth rates are compared for the massive coral species Favia pallida (Dana), Goniastrea retiformis (Lamarck), and Porites lutea Milne Edwards & Haime at Enewetak Atoll. Marshall Islands. Goniastrea retiformis is the densest of the three species and has an intermediate growth rate; Porites lutea grows more rapidly. All three grow indeterminately at a declining rate with increasing depth.The high-density portion of annual band couplets is produced during the late summer and fall when water temperatures are highest and possibly the availability of light is reduced, and the low density portion is formed during periods of seasonally lower water temperatures and possibly higher availability of light. A similar pattern is found in three massive coral species from Belize.The high density portions of annual bands account for a greater proportion of linear and mass growth in deeper water and in corals with relatively slow growth rates. I predict that linear growth rates will be highest where conditions are most favorable for deposition of the low density portion.Geographical patterns of coral density banding based on the literature are discussed and a model is proposed relating the interplay of light availability and water temperature to the production of high and low density skeletal bands.     

Structure and growth rates of the high-latitude coral: <Emphasis Type="Italic">Plesiastrea versipora</Emphasis>

The high-latitude coral species Plesiastrea versipora was investigated to identify growth rates in colonies over 1 m in diameter. Six colonies from two temperate gulfs (latitudes of 33°–35°S) in Southern Australia were examined using X-ray, luminescence and ²³⁸U/²³⁰Th dating techniques. Annual density bands were present in each coral but varied in width and definition, suggesting different linear extension and calcification rates. Differences in density band width were observed at the local scale (amongst colonies on the same reef) and regional scales (between the two gulfs). Extension rates of the P. versipora colonies examined in this study varied between 1.2 and 7 mm per year, which are amongst the slowest growth rates reported for hermatypic corals. As only one of the six P. versipora colonies had obvious luminescent banding, we conclude that luminescent banding is not an accurate chronological marker in this species of temperate water coral. Coral age estimates derived from counting density bands in X-radiographs ranged from 90 to 320 years for the six colonies studied. U-Th ages from the same colonies determined by high-precision multi-collector inductively coupled plasma mass spectrometer established radiometric ages between 105 and 381 years. The chronological variation in absolute ages between the two techniques varied between 2 and 19% in different colonies, with the lowest growth rates (~1 mm) displaying the greatest variation between density band age and radiometric U-Th age. This result implies that the age of P. versipora and other slow-growing corals cannot be determined accurately from density bands alone. The outcome of this research demonstrates that P. versipora may be useful as a paleoclimate archive, recording several centuries in a single colony in high-latitude environments (corals found in latitudes greater than 30° in either hemisphere), where other well-established coral climate archives, such as Porites, do not occur.     

Experimental evidence for high temperature stress as the cause of El Niño-coincident coral mortality

High temperature tolerance experiments performed on Pocillopora damicornis, a major reef-building coral in the tropical eastern Pacific, resulted in loss of zooxanthellae, histopathological abnormalities, and mortality similar to that observed during the severe 1982–83 El Niño-Southern Oscillation (ENSO) event. Coral vitality declined significantly at 30–32°C during a 10-week period, but remained high at normal temperatures (26–28°C). Laboratory time courses to coral morbidity and death were similar to those observed in the field. Experimental high temperatures had a greater negative effect on corals from the Gulf of Panama, which experiences seasonally cool upwellings, than on corals from the nonupwelling Gulf of Chiriqui. The condition of obligate symbiotic crustaceans (Trapezia, Alpheus) associated with experimental corals declined with their host's declining condition. All Gulf of Panama corals subjected to 32°C were dead after 5 weeks, and all of their associated crustacean symbionts were dead after 9 weeks. Gulf of Chiriqui corals at 30°C survived for 9 weeks and 42% of their crustacean symbionts were still alive after 10 weeks. Coral mortality in the Gulf of Panama was significantly higher (68.5%) after El Niño warming than after subsequent episodes of unusually intense cool upwellings (10.4%). Low temperature stress (cool currents and upwelling) has been generally suggested as the critical limiting condition that prevents extensive coral reef development in the eastern Pacific. Our results suggest that infrequent but severe ENSO sea warming events also may limit reef development in this region.     

Fluorescent and skeletal density banding in Porites lutea from Papua New Guinea and Indonesia

Shallow water Porites lutea corals were collected along two transects normal to mainland shorelines, parallel to gradients in water quality: one, 7 km long, near Motupore Island in South Papua New Guinea, the other, 70 km long, from Jakarta Bay along the Pulau Seribu chain in the Java Sea. The corals were slabbed and studies were made of skeletal density bands as revealed by X-ray photography and fluorescent bands as revealed by ultraviolet light. Water quality measurements and rain-fall data were assembled for the two areas and related to skeletal banding patterns. For both areas, with increasing distance form mainland there is a decrease in overall brightness of fluorescence in corals and an increase in the contrast between bright and dull fluorescent bands. Fluorescence is bright, but seasonal banding is obscure in corals within about 2 km of stream mouths at Motopure and about 5 km of the coast in Jakarta Bay; this suggests that, despite low freshwater run-off during dry seasons, there are sufficient organic compounds which cause fluorescence in coral skeletons, to swamp seasonal effects. During the wet seasons, deluges of freshwater consequent on mainland rainfall of greater than about 150 mm/ month extend at least 7 km offshore in the Motupore area and perhaps tens of kilometres into Java Sea, giving distinctive bright and dull fluorescent banding in off-shore corals. The fluorescent banding pattern within corals on the Motupore reefs is similar in most corals along the transect and it correlates well with the Port Moresby monthly rainfall data. This relationship suggests that the same body (or bodies) of freshwater affect all reefs of the area during the wet season. The fluorescent banding in Java Sea corals does not show a precise correlation with either mainland or island monthly rainfall data; indeed the pattern of fluorescent banding on Pulau Seribu can only be matched in corals from reefs less than about 25 km apart. This suggests that in this area discrete water bodies carrying the relevant organic acids for coral fluorescence affect the fringing reefs on the chain of islands. Comparisons of fluorescent and density banding have revealed that for these areas, in general, periods of high freshwater run-off are times of deposition of less dense skeleton in Porites lutea corals.     

The Possible Role of Cyanobacterial Filaments in Coral Black Band Disease Pathology

Black band disease (BBD), characterized by a black mat or line that migrates across a coral colony leaving behind it a bare skeleton, is a persistent disease affecting massive corals worldwide. Previous microscopic and molecular examination of this disease in faviid corals from the Gulf of Eilat revealed a number of possible pathogens with the most prominent being a cyanobacterium identified as Pseudoscillatoria coralii. We examined diseased coral colonies using histopathological and molecular methods in order to further assess the possible role of this cyanobacterium, its mode of entry, and pathological effects on the coral host tissues. Affected areas of colonies with BBD were sampled for examination using both light and transmission electron microscopies. Results showed that this dominant cyanobacterium was found on the coral surface, at the coral–skeletal interface, and invading the polyp tissues and gastrovascular cavity. Although tissues surrounding the invasive cyanobacterial filaments did not show gross morphological alterations, microscopic examination revealed that the coral cells surrounding the lesion were dissociated, necrotic, and highly vacuolated. No amoebocytes were evident in the mesoglea of affected tissues suggesting a possible repression of the coral immune response. Morphological and molecular similarity of the previously isolated BBD-associated cyanobacterium P. coralii to the current samples strengthens the premise that this species is involved in the disease in this coral. These results indicate that the cyanobacteria may play a pivotal role in this disease and that the mode of entry may be via ingestion, penetrating the coral via the gastrodermis, as well as through the skeletal–tissue interface.     

Simultaneous extension of both basic microstructural components in scleractinian coral skeleton during night and daytime,visualized by in situ 86Sr pulse labeling

Using in situ (12 h) pulse-labeling of scleractinian coral aragonitic skeleton with stable ⁸⁶Sr isotope, the diel pattern of skeletal extension was investigated in the massive Porites lobata species, grown at 5 m depth in the Gulf of Eilat. Several microstructural aspects of coral biomineralization were elucidated, among which the most significant is simultaneous extension of the two basic microstructural components Rapid Accretion Deposits (RAD; also called Centers of Calcification) and Thickening Deposits (TD; also called fibers), both at night and during daytime. Increased thickness of the ⁸⁶Sr-labeled growth-front in the RADs compared to the adjacent TDs revealed that in this species RADs extend on average twice as fast as TDs. At the level of the individual corallite, skeletal extension is spatially highly heterogeneous, with sporadic slowing or cessation depending on growth directions and skeletal structure morphology. Daytime photosynthesis by symbiotic dinoflagellates is widely acknowledged to substantially increase calcification rates at the colony and the corallite level in reef-building corals. However, in our study, the average night-time extension rate (visualized in three successive 12 h pulses) was similar to the average daytime extension (visualized in the initial 12 h pulse), in all growth directions and skeletal structures. This research provides a platform for further investigations into the temporal calibration of coral skeletal extension via cyclic growth increment deposition, which is a hallmark of coral biomineralization.     

Oxygen and Heterotrophy Affect Calcification of the Scleractinian Coral Galaxea fascicularis

Heterotrophy is known to stimulate calcification of scleractinian corals, possibly through enhanced organic matrix synthesis and photosynthesis, and increased supply of metabolic DIC. In contrast to the positive long-term effects of heterotrophy, inhibition of calcification has been observed during feeding, which may be explained by a temporal oxygen limitation in coral tissue. To test this hypothesis, we measured the short-term effects of zooplankton feeding on light and dark calcification rates of the scleractinian coral Galaxea fascicularis (n = 4) at oxygen saturation levels ranging from 13 to 280%. Significant main and interactive effects of oxygen, heterotrophy and light on calcification rates were found (three-way factorial repeated measures ANOVA, p<0.05). Light and dark calcification rates of unfed corals were severely affected by hypoxia and hyperoxia, with optimal rates at 110% saturation. Light calcification rates of fed corals exhibited a similar trend, with highest rates at 150% saturation. In contrast, dark calcification rates of fed corals were close to zero under all oxygen saturations. We conclude that oxygen exerts a strong control over light and dark calcification rates of corals, and propose that in situ calcification rates are highly dynamic. Nevertheless, the inhibitory effect of heterotrophy on dark calcification appears to be oxygen-independent. We hypothesize that dark calcification is impaired during zooplankton feeding by a temporal decrease of the pH and aragonite saturation state of the calcifying medium, caused by increased respiration rates. This may invoke a transient reallocation of metabolic energy to soft tissue growth and organic matrix synthesis. These insights enhance our understanding of how oxygen and heterotrophy affect coral calcification, both in situ as well as in aquaculture.     

Growth characteristics of the reef-building coral Porites astreoides under different environmental conditions in the Western Atlantic

Skeletal extension (3.67 ± 0.65 mm year⁻¹), density (1.49 ± 0.16 g cm⁻³), and calcification rate (0.55 ± 0.12 g cm⁻² year⁻¹) were determined using annual growth bands of Porites astreoides skeletons collected in three different reef systems in the Western Atlantic. The corals showed a low-density annual growth band at their apex, and seasonal timing of low and high-density band formation in P. astreoides appears to be similar at the three study sites in the Western Atlantic. The range of values presented here, for the three growth variables, spans the known range of skeletal-growth variability in P. astreoides for the Western Atlantic. The relationships between the growth parameters were similar to those previously described by other authors for massive Porites species from the Indo-Pacific, suggesting that P. astreoides has the same growth strategy, primarily investing calcification resources in extension rate. It is noteworthy that the P. astreoides population growing off the northwest coast of Cuba had similar growth characteristics as populations from the Caribbean region which were different from populations in the Gulf of Mexico, which seem to be isolated and adapted for growth at higher average sea-surface temperatures.     

The skeletal structure of Desmophyllum cristagalli: the use of deep-water corals in sclerochronology

Skeletal banding has been found in the deep-water scleractinian coral Desmophyllum cristagalli , an important animal in studies of climate change. This banding pattern sheds light on skeletogenesis and suggests methods by which the record of climate change contained within the coral skeletons may be interpreted. A central wall built of trabeculae forms the interior of the septa and rings the theca. Lamellae form a sheath over the trabecular frame, showing continuity from thecal edge to septum. Skeletal bands are added by the tissue layer, which overlaps and seals the internal coral and upper portion of the outer theca. Truncated inner bands on the outer theca indicate a pattern of skeletal deposition and dissolution dependent on the presence or absence of the live tissue layer. A long-term record will be difficult to collect from D. cristagalli since lamellae are less than 10 μm thick and band position is unpredictable. Density banding in shallow-water coral skeletons has long been recognized as a valuable paleo-oceanographic tool, and deep-water corals are now being used to reconstruct deep-ocean environments. Pattern of skeletal growth must be carefully considered if deep-water corals are to be used as proxy climate recorders.     

Ocean acidification bends the mermaid's wineglass

Ocean acidification lowers the saturation state of calcium carbonate, decreasing net calcification and compromising the skeletons of organisms such as corals, molluscs and algae. These calcified structures can protect organisms from predation and improve access to light, nutrients and dispersive currents. While some species (such as urchins, corals and mussels) survive with decreased calcification, they can suffer from inferior mechanical performance. Here, we used cantilever beam theory to test the hypothesis that decreased calcification would impair the mechanical performance of the green alga Acetabularia acetabulum along a CO₂ gradient created by volcanic seeps off Vulcano, Italy. Calcification and mechanical properties declined as calcium carbonate saturation fell; algae at 2283 µatm CO₂ were 32% less calcified, 40% less stiff and 40% droopier. Moreover, calcification was not a linear proxy for mechanical performance; stem stiffness decreased exponentially with reduced calcification. Although calcifying organisms can tolerate high CO₂ conditions, even subtle changes in calcification can cause dramatic changes in skeletal performance, which may in turn affect key biotic and abiotic interactions.     

Calcification by juvenile corals under heterotrophy and elevated CO2

Ocean acidification (OA) threatens the existence of coral reefs by slowing the rate of calcium carbonate (CaCO₃) production of framework-building corals thus reducing the amount of CaCO₃ the reef can produce to counteract natural dissolution. Some evidence exists to suggest that elevated levels of dissolved inorganic nutrients can reduce the impact of OA on coral calcification. Here, we investigated the potential for enhanced energetic status of juvenile corals, achieved via heterotrophic feeding, to modulate the negative impact of OA on calcification. Larvae of the common Atlantic golf ball coral, Favia fragum, were collected and reared for 3 weeks under ambient (421 μatm) or significantly elevated (1,311 μatm) CO₂ conditions. The metamorphosed, zooxanthellate spat were either fed brine shrimp (i.e., received nutrition from photosynthesis plus heterotrophy) or not fed (i.e., primarily autotrophic). Regardless of CO₂ condition, the skeletons of fed corals exhibited accelerated development of septal cycles and were larger than those of unfed corals. At each CO₂ level, fed corals accreted more CaCO₃ than unfed corals, and fed corals reared under 1,311 μatm CO₂ accreted as much CaCO₃ as unfed corals reared under ambient CO₂. However, feeding did not alter the sensitivity of calcification to increased CO₂; ? calcification/?Ω was comparable for fed and unfed corals. Our results suggest that calcification rates of nutritionally replete juvenile corals will decline as OA intensifies over the course of this century. Critically, however, such corals could maintain higher rates of skeletal growth and CaCO₃ production under OA than those in nutritionally limited environments.