Calcification in Three Common Calcified Algae from Phuket, Thailand: Potential Relevance on Seawater Carbonate Chemistry and Link to Photosynthetic Process

Calcifying macroalgae contribute significantly to the structure and function of tropical marine ecosystems. Their calcification and photosynthetic processes are not well understood despite their critical role in marine carbon cycles and high vulnerability to environmental changes. This study aims to provide a better understanding of the macroalgal calcification process, focusing on its relevance concerning seawater carbonate chemistry and its relationship to photosynthesis in three dominant calcified macroalgae in Thailand, Padina boryana, Halimeda macroloba and Halimeda opuntia. Morphological and microstructural attributes of the three macroalgae were analyzed and subsequently linked to their calcification rates and responses to inhibition of photosynthesis. In the first experiment, seawater pH, total alkalinity and total dissolved inorganic carbon were measured after incubation of the macroalgae in the light and after equilibration of the seawater with air. Estimations of carbon uptake into photosynthesis and calcification and carbon release into air were obtained thereafter. Our results provide evidence that calcification of the three calcified macroalgae is a potential source of CO2, where calcification by H. opuntia and H. macroloba leads to a greater release of CO2 per biomass weight than P. boryana. Nevertheless, this capacity is expected to vary on a diurnal basis, as the second experiment indicates that calcification is highly coupled to photosynthetic activity. Lower pH as a result of inhibited photosynthesis under darkness imposes more negative effects on H. opuntia and H. macroloba than on P. boryana, implying that they are more sensitive to acidification. These effects were worsened when photosynthesis was inhibited by 3-(3,4-dichlorophenyl)-1,1-dimethylurea, highlighting the significance of photosynthetic electron transport-dependent processes. Our findings suggest that estimations of the amount of carbon stored in the vegetated marine ecosystems should account for macroalgal calcification as a potential carbon source while considering diurnal variations in photosynthesis and seawater pH in a natural setting.

A Unique Diel Pattern in Carbonate Chemistry in the Seagrass Meadows of Dongsha Island: The Enhancement of Metabolic Carbonate Dissolution in a Semienclosed Lagoon

In contrast to other seagrass meadows where seawater carbonate chemistry generally shows strong diel variations with higher pH but lower partial pressure of CO2 (pCO2) during the daytime and lower pH but higher pCO2 during nighttime due to the alternation in photosynthesis and respiration, the seagrass meadows of the inner lagoon (IL) on Dongsha Island had a unique diel pattern with extremely high pH and low pCO2 across a diel cycle. We suggest that this distinct diel pattern in pH and pCO2 could be associated with the enhancement of total alkalinity (TA) production coupled to carbonate sediment dissolution in a semienclosed lagoon. The confinement of the IL may hamper water exchange and seagrass detritus export to the adjacent open ocean, which may result in higher organic matter loading to the sediments, and longer residence time of the water in the IL, accompanied by microbial respiration (both aerobic and anaerobic) that may reduce carbonate saturation level to drive carbonate dissolution and thus TA elevation, thereby forming such a unique diel pattern in carbonate chemistry. This finding further highlights the importance of considering TA production through metabolic carbonate dissolution when evaluating the potential of coastal blue carbon ecosystems to buffer ocean acidification and to absorb atmospheric CO2, in particular in a semienclosed setting.

Reduced H+ channel activity disrupts pH homeostasis and calcification in coccolithophores at low ocean pH

Coccolithophores produce the bulk of ocean biogenic calcium carbonate but this process is predicted to be negatively affected by future ocean acidification scenarios. Since coccolithophores calcify intracellularly, the mechanisms through which changes in seawater carbonate chemistry affect calcification remain unclear. Here we show that voltage-gated H+ channels in the plasma membrane of Coccolithus braarudii serve to regulate pH and maintain calcification under normal conditions, but have greatly reduced activity in cells acclimated to low pH. This disrupts intracellular pH homeostasis and impairs the ability of C. braarudii to remove H+ generated by the calcification process, leading to specific coccolith malformations. These coccolith malformations can be reproduced by pharmacological inhibition of H+ channels. Heavily-calcified coccolithophore species such as C. braarudii, which make the major contribution to carbonate export to the deep ocean, have a large intracellular H+ load and are likely to be most vulnerable to future decreases in ocean pH.

Global coral reef ecosystems exhibit declining calcification and increasing primary productivity

Long-term coral reef resilience to multiple stressors depends on their ability to maintain positive calcification rates. Estimates of coral ecosystem calcification and organic productivity provide insight into the environmental drivers and temporal changes in reef condition. Here, we analyse global spatiotemporal trends and drivers of coral reef calcification using a meta-analysis of ecosystem-scale case studies. A linear mixed effects regression model was used to test whether ecosystem-scale calcification is related to seasonality, methodology, calcifier cover, year, depth, wave action, latitude, duration of data collection, coral reef state, Ωar, temperature and organic productivity. Global ecosystem calcification estimated from changes in seawater carbonate chemistry was driven primarily by depth and benthic calcifier cover. Current and future declines in coral cover will significantly affect the global reef carbonate budget, even before considering the effects of sub-lethal stressors on calcification rates. Repeatedly studied reefs exhibited declining calcification of 4.3 ± 1.9% per year (x̄ = 1.8 ± 0.7 mmol m−2 d−1 yr−1), and increasing organic productivity at 3.0 ± 0.8 mmol m−2 d−1 per year since 1970. Therefore, coral reef ecosystems are experiencing a shift in their essential metabolic processes of calcification and photosynthesis, and could become net dissolving worldwide around 2054.

The anthropogenic environmental impacts and changes in the tropical Atlantic - a high resolution Cuban coral time series over 154 years

<p>Changes in the surface ocean pH and temperature caused by the uptake of anthropogenic CO<sub>2</sub> are posing a threat to calcifying marine organisms. Recent studies have observed significant impacts on coral reef ecosystems with impaired carbonate skeletal growth and decreased calcification due to acidifying oceans. In situ measurements from buoys, ships, and remote observations by satellite of sea surface temperature, salinity, and ocean’s carbonate chemistry are sparse and only date back a few decades. The current coverage of observations for the northwestern Cuban coastal waters provides hence an incomplete picture of natural climate variability over interannual to interdecadal timescales, showing the need for high resolution climate archives.</p><p>Cuba is situated between densely populated landmasses of North and South America offering a unique environment to study multiple aspects of anthropogenic activity across the region as well as their interconnectivity.</p><p>A massive coral, <em>Siderastrea siderea</em>, from Cuba’s northwestern coast, was used as a natural archive to reconstruct bimonthly changes in SST, and carbonate chemistry through a multi-proxy approach since preindustrial times.</p><p>Preliminary results indicate a decrease in δ<sup>18</sup>O of 0.32 ‰ over 154 years since 1852,  indicating warming and/or freshening of the surface water over this period. Over the same time period, the δ<sup>11</sup>B ratio decreased by ca. 1.6 ‰, translating into a decrease of 0.1 on the pH scale, reflecting the acidification of the northwestern Cuban coastal waters. Furthermore, an accelerating decrease of coral δ<sup>13</sup>C from the 1850s to 2005 of 1.5 ‰ demonstrates the anthropogenic imprint due to increased fossil fuel combustion. Further investigation and the comparison to trace elements indicate possible baseline shifts in regional seawater carbonate chemistry that have been affected by anthropogenic activity.</p>

Production and calcification variations of the key coccolithophore species Gephyrocapsa during the Late Pleistocene (MIS 14 to MIS 7)

<p>There is an increasing interest in understanding the role of coccolithophores, a group of major calcifying phytoplankton, in the marine carbon cycle: they have a dual contribution to the operation of the carbonate and biological pumps during their lifecycle. How the recent changes in seawater carbonate chemistry are affecting their production and calcification is a matter of debate in the scientific community. Culture experiments suggest that modern coccolithophore species (<em>Emiliania huxleyi</em>) is sensitive to such variations. Conversely, could past evolutionary or adaptative changes in the most important coccolithophore species have an impact on ocean chemistry?  </p><p>We focus on the interval comprising the MIS 14 to 7 (Mid-Brunhes, Pleistocene) when a remarkable increase in the amplitude of glacial/interglacial atmospheric CO<sub>2</sub> was recorded. We analyzed (i) the composition of the dominant coccolithophore <em>Gephyrocapsa</em> assemblages and (ii) the morphometric parameters (length, mass, and thickness) of its coccoliths (carbonated scales) <span>in samples from a set of sediment cores (Sites IODP U1314, U1385and ODP 925 and 977) located in a north-south transect in the North Atlantic and the western Mediterranean Sea. We estimated the primary productivity conditions at the different regions and explore methodological approaches to measure the calcification of <em>Gephyrocapsa</em> coccoliths.</span></p><p>Preliminary results show a correlation between the abundance of coccoliths, assemblage composition, and coccolith morphology at different regions. A comparison with geochemical and sedimentological records suggests a significant role of <em>Gephyrocapsa</em> coccolithophore in marine organic and carbonate production throughout the interval. These observations open the discussion about the existence of a global environmental relationship between coccolithophore assemblages and coccolith morphometrical variations, but also, a possible impact of the changes in the <em>Gephyrocapsa</em> production and calcification on the ocean chemistry.</p>

Lateral, Vertical, and Temporal Variability of Seawater Carbonate Chemistry at Hog Reef, Bermuda

Spatial and temporal carbonate chemistry variability on coral reefs is influenced by a combination of seawater hydrodynamics, geomorphology, and biogeochemical processes, though their relative influence varies by site. It is often assumed that the water column above most reefs is well-mixed with small to no gradients outside of the benthic boundary layer. However, few studies to date have explored the processes and properties controlling these multi-dimensional gradients. Here, we investigated the lateral, vertical, and temporal variability of seawater carbonate chemistry on a Bermudan rim reef using a combination of spatial seawater chemistry surveys and autonomous in situ sensors. Instruments were deployed at Hog Reef measuring current flow, seawater temperature, salinity, pHT, pCO2, dissolved oxygen (DO), and total alkalinity (TA) on the benthos, and temperature, salinity, DO, and pCO2 at the surface. Water samples from spatial surveys were collected from surface and bottom depths at 13 stations covering ∼3 km2 across 4 days. High frequency temporal variability in carbonate chemistry was driven by a combination of diel light and mixed semi-diurnal tidal cycles on the reef. Daytime gradients in DO between the surface and the benthos suggested significant water column production contributing to distinct diel trends in pHT, pCO2, and DO, but not TA. We hypothesize these differences reflect the differential effect of biogeochemical processes important in both the water column and benthos (organic carbon production/respiration) vs. processes mainly occurring on the benthos (calcium carbonate production/dissolution). Locally at Hog Reef, the relative magnitude of the diel variability of organic carbon production/respiration was 1.4–4.6 times larger than that of calcium carbonate production/dissolution, though estimates of net organic carbon production and calcification based on inshore-offshore chemical gradients revealed net heterotrophy (−118 ± 51 mmol m–2 day–1) and net calcification (150 ± 37 mmol CaCO3 m–2 day–1). These results reflect the important roles of time and space in assessing reef biogeochemical processes. The spatial variability in carbonate chemistry parameters was larger laterally than vertically and was generally observed in conjunction with depth gradients, but varied between sampling events, depending on time of day and modifications due to current flow.