Mmol CaCO3 Research Articles

Ocean acidification enhances primary productivity and nocturnal carbonate dissolution in intertidal rock pools

Abstract. Human CO2 emissions are modifying ocean carbonate chemistry, causing ocean acidification and likely already impacting marine ecosystems. In particular, there is concern that coastal, benthic calcifying organisms will be negatively affected by ocean acidification, a hypothesis largely supported by laboratory studies. The inter-relationships between carbonate chemistry and marine calcifying communities in situ are complex, and natural mesocosms such as tidal pools can provide useful community-level insights. In this study, we manipulated the carbonate chemistry of intertidal pools to investigate the influence of future ocean acidification on net community production (NCP) and calcification (NCC) at emersion. Adding CO2 at the start of the tidal emersion to simulate future acidification (+1500 µatm pCO2, target pH 7.5) modified net production and calcification rates in the pools. By day, pools were fertilized by the increased CO2 (+20 % increase in NCP, from 10 to 12 mmol O2 m−2 h−1), while there was no measurable impact on NCC. During the night, pools experienced net community dissolution (NCC < 0), even under present-day conditions, when waters were supersaturated with regard to aragonite. Adding CO2 to the pools increased nocturnal dissolution rates by 40 % (from −0.7 to −1.0 mmol CaCO3 m−2 h−1) with no consistent impact on nocturnal community respiration. Our results suggest that ocean acidification is likely to alter temperate intertidal community metabolism on sub-daily timescales, enhancing both diurnal community production and nocturnal calcium carbonate dissolution.

Decadal-scale variation in coral calcification on coral-depleted Caribbean reefs

Over recent decades, many Caribbean reefs have transitioned to states where stony corals are no longer spatially dominant. The community dynamics culminating in this outcome are well known, but its functional implications remain incompletely understood. Here we used annual surveys from 1992 to 2019 to describe coral communities at 6 sites off St. John, US Virgin Islands, and explored how their ecological dynamics interact with their capacity to sustain estimated coral community calcification (G, kg CaCO3 m-2 yr-1). These communities had low coral cover (≤4.4%), but they changed through small and incremental events that summed to a slight decline in coral cover and changes in species assemblages favoring biotic homogenization and weedy species. Estimated coral G remained low, between 0.3 and 1.3 kg CaCO3 m-2 yr-1 (8.2-35.6 mmol CaCO3 m-2 d-1), but it differed among sites and years. The dominant contributors to G were Siderastrea siderea (1 site), Porites astreoides (1 site), and Orbicella spp. (4 sites), but higher G only occurred where Orbicella spp. remained relatively common; G dramatically declined at 1 site when the abundance of this genus decreased. These results suggest that some coral-depleted reefs may maintain low G that could be sufficient to avoid transitions into net negative budget states, provided that biological and physical erosion and dissolution of CaCO3 (not recorded here) are minimal. Further mortalities of the few coral species remaining on these reefs through disturbances like stony coral tissue loss disease would compromise this delicate production-erosion balance, and likely see transitions of such reefs into negative carbonate budget states.

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.

Ocean Acidification and Short‐Term Organic Matter Enrichment Alter Coral Reef Sediment Metabolism Through Different Pathways

AbstractOcean acidification (OA) and organic matter (OM) enrichment (due to coastal eutrophication) could act in concert to shift coral reef carbonate sediments from a present state of net calcification to a future state of net dissolution, but no studies have examined the combined effect of these stressors on sediment metabolism and dissolution. This study used 22‐h incubations in flume aquaria with captive sediment communities to measure the combined effect of elevated pCO2 (representing Ocean Acidification) and particulate organic carbon (representing coastal eutrophication) on coral reef sediment gross primary productivity (GPP), respiration (R), and net calcification (Gnet). Relative to control sediment communities, both OA (pCO2 ~ 1,000 μatm) and OM enrichment (~ +40 μmol C L−1) significantly decreased rates of sediment Gnet by 1.16 and 0.18 mmol CaCO3 m−2 h−1, respectively, but the mechanism behind this decrease differed. The OA‐mediated transition to net dissolution was physiochemical, as rates of GPP and R remained unaffected and dissolution was solely enhanced by a decline in the aragonite saturation state (Ωarg) of the overlying water column and the physical factors governing the pore water exchange rate with this overlying water column. In contrast, the OM‐mediated decline in Gnet was due to a decline in the overlying seawater Ωarg due to the increased respiratory addition of CO2. The decrease in Gnet in response to a combination of both stressors was additive (−0.09 mmol CaCO3 m−2 h−1 relative to OA alone), but this decrease did not significantly differ from the individual effect of either stressor. In this study OA was the primary driver of future carbonate sediment dissolution, but longer‐term experiments with chronic organic matter enrichment are required.

Evaluating the potential for autonomous measurements of net community production and calcification as a tool for monitoring coral restoration

As coral restoration efforts increase globally, there is a growing need to not only increase post-restoration monitoring, but also advance reef restoration monitoring methods. Utilizing autonomous technology to compliment manual, SCUBA-based monitoring will diversify the types of data available to coral restoration practitioners and aid in determining the efficacy of restoration efforts. This study sought to investigate how existing reef monitoring technologies can be applied to coral restoration to improve monitoring resolution and assess restoration progress. The Benthic Ecosystem and Acidification Measurement System, which uses the gradient flux approach to measure benthic community metabolism, was used to monitor two arrays of nursery grown Acropora cervicornis within an offshore coral nursery in the Florida Keys. The first deployment monitored corals arranged in a density mimicking pre-restoration coral cover, while the second deployment monitored corals arranged in a density mimicking a reef site recently restored with nursery-grown A. cervicornis. The post-restoration density demonstrated a 36% increase in the observed ratio of net community calcification to net community production as compared to the pre-restoration density. Additionally, the post-restoration density demonstrated net accretion throughout the observation period (20 mmol CaCO3 m−2d−1) as compared to the pre-restoration density which experienced net dissolution (−5.0 mmol CaCO3 m−2d−1). Overall, the results of this study are promising indicators that metabolic monitoring could one day be widely utilized within the coral restoration field to remotely monitor benthic composition changes associated with coral restoration progress over time, providing valuable information to restoration practitioners, stakeholders, and resource managers.

In-situ incubation of a coral patch for community-scale assessment of metabolic and chemical processes on a reef slope.

Anthropogenic pressures threaten the health of coral reefs globally. Some of these pressures directly affect coral functioning, while others are indirect, for example by promoting the capacity of bioeroders to dissolve coral aragonite. To assess the coral reef status, it is necessary to validate community-scale measurements of metabolic and geochemical processes in the field, by determining fluxes from enclosed coral reef patches. Here, we investigate diurnal trends of carbonate chemistry, dissolved organic carbon, oxygen, and nutrients on a 20 m deep coral reef patch offshore from the island of Saba, Dutch Caribbean by means of tent incubations. The obtained trends are related to benthic carbon fluxes by quantifying net community calcification (NCC) and net community production (NCP). The relatively strong currents and swell-induced near-bottom surge at this location caused minor seawater exchange between the incubated reef and ambient water. Employing a compensating interpretive model, the exchange is used to our advantage as it maintains reasonably ventilated conditions, which conceivably prevents metabolic arrest during incubation periods of multiple hours. No diurnal trends in carbonate chemistry were detected and all net diurnal rates of production were strongly skewed towards respiration suggesting net heterotrophy in all incubations. The NCC inferred from our incubations ranges from −0.2 to 1.4 mmol CaCO3 m−2 h−1 (−0.2 to 1.2 kg CaCO3 m−2 year−1) and NCP varies from −9 to −21.7 mmol m−2 h−1 (net respiration). When comparing to the consensus-based ReefBudget approach, the estimated NCC rate for the incubated full planar area (0.36 kg CaCO3 m−2 year−1) was lower, but still within range of the different NCC inferred from our incubations. Field trials indicate that the tent-based incubation as presented here, coupled with an appropriate interpretive model, is an effective tool to investigate, in situ, the state of coral reef patches even when located in a relatively hydrodynamic environment.

Primary Production and Calcification Rates of Algae‐Dominated Reef Flat and Seagrass Communities

AbstractMonitoring variability in coral reef primary production and calcification is needed to understand changes over time and between reef systems, which helps separate differences due to natural and/or anthropogenic factors happening now and in the future. This study measured net productivity and calcification for two reef systems at Shark Bay, Heron Reef in the southern Great Barrier Reef and Saipan Lagoon, Commonwealth of the Northern Mariana Islands. Net primary productivity and calcification were strongly correlated for reef flats with an adjusted R2 = 0.66. Night time dissolution occurred at Shark Bay reef flat with an average of −12.66 mmol CaCO3 · m−2 · hr−1, while calcification increased at night for the Saipan reef flat. For both reef flat sites, net productivity from oxygen flux was much lower than rates calculated from change in dissolved inorganic carbon. This study provided the first baseline estimates of net productivity and calcification for a reef flat and seagrass community in Saipan Lagoon. The seagrass community had the lowest productivity of all sites. However, the high presence of calcareous algae at the site highlights the need for more research on the carbonate chemistry of these habitats. All sites had high net productivity that was most likely associated with the dominant presence of algae.

Community production modulates coral reef pH and the sensitivity of ecosystem calcification to ocean acidification

AbstractCoral reefs are built of calcium carbonate (CaCO3) produced biogenically by a diversity of calcifying plants, animals, and microbes. As the ocean warms and acidifies, there is mounting concern that declining calcification rates could shift coral reef CaCO3 budgets from net accretion to net dissolution. We quantified net ecosystem calcification (NEC) and production (NEP) on Dongsha Atoll, northern South China Sea, over a 2 week period that included a transient bleaching event. Peak daytime pH on the wide, shallow reef flat during the nonbleaching period was ∼8.5, significantly elevated above that of the surrounding open ocean (∼8.0–8.1) as a consequence of daytime NEP (up to 112 mmol C m−2 h−1). Diurnal‐averaged NEC was 390 ± 90 mmol CaCO3 m−2 d−1, higher than any other coral reef studied to date despite comparable calcifier cover (25%) and relatively high fleshy algal cover (19%). Coral bleaching linked to elevated temperatures significantly reduced daytime NEP by 29 mmol C m−2 h−1. pH on the reef flat declined by 0.2 units, causing a 40% reduction in NEC in the absence of pH changes in the surrounding open ocean. Our findings highlight the interactive relationship between carbonate chemistry of coral reef ecosystems and ecosystem production and calcification rates, which are in turn impacted by ocean warming. As open‐ocean waters bathing coral reefs warm and acidify over the 21st century, the health and composition of reef benthic communities will play a major role in determining on‐reef conditions that will in turn dictate the ecosystem response to climate change.

Antagonistic Effects of Ocean Acidification and Rising Sea Surface Temperature on the Dissolution of Coral Reef Carbonate Sediments

Increasing atmospheric CO2 is raising sea surface temperature (SST) and increasing seawater CO2 concentrations, resulting in a lower oceanic pH (ocean acidification; OA), which is expected to reduce the accretion of coral reef ecosystems. Although sediments comprise most of the calcium carbonate (CaCO3) within coral reefs, no in situ studies have looked at the combined effects of increased SST and OA on the dissolution of coral reef CaCO3 sediments. In situ benthic chamber incubations were used to measure dissolution rates in permeable CaCO3 sands under future OA and SST scenarios in a coral reef lagoon on Australia’s Great Barrier Reef (Heron Island). End of century (2100) simulations (temperature +2.7°C and pH -0.3) shifted carbonate sediments from net precipitating to net dissolving. Warming increased the rate of benthic respiration (R) by 29% per 1°C and lowered the ratio of productivity to respiration (P/R; ΔP/R = -0.23), which increased the rate of CaCO3 sediment dissolution (average net increase of 18.9 mmol CaCO3 m-2 d-1 for business as usual scenarios). This is most likely due to the influence of warming on benthic P/R which, in turn, was an important control on sediment dissolution through the respiratory production of CO2. The effect of increasing CO2 on CaCO3 sediment dissolution (average net increase of 6.5 mmol CaCO3 m-2 d-1 for business as usual scenarios) was significantly less than the effect of warming. However, the combined effect of increasing both SST and pCO2 on CaCO3 sediment dissolution was non-additive (average net increase of 5.6 mmol CaCO3 m-2 d-1) due to the different responses of the benthic community. This study highlights that benthic biogeochemical processes such as metabolism and associated CaCO3 sediment dissolution respond rapidly to changes in SST and OA, and that the response to multiple environmental changes are not necessarily additive.

Multiple driving factors explain spatial and temporal variability in coral calcification rates on the Bermuda platform

Experimental studies have shown that coral calcification rates are dependent on light, nutrients, food availability, temperature, and seawater aragonite saturation (Ω arag), but the relative importance of each parameter in natural settings remains uncertain. In this study, we applied Calcein fluorescent dyes as time indicators within the skeleton of coral colonies (n = 3) of Porites astreoides and Diploria strigosa at three study sites distributed across the northern Bermuda coral reef platform. We evaluated the correlation between seasonal average growth rates based on coral density and extension rates with average temperature, light, and seawater Ω arag in an effort to decipher the relative importance of each parameter. The results show significant seasonal differences among coral calcification rates ranging from summer maximums of 243 ± 58 and 274 ± 57 mmol CaCO3 m−2 d−1 to winter minimums of 135 ± 39 and 101 ± 34 mmol CaCO3 m−2 d−1 for P. astreoides and D. strigosa, respectively. We also placed small coral colonies (n = 10) in transparent chambers and measured the instantaneous rate of calcification under light and dark treatments at the same study sites. The results showed that the skeletal growth of D. strigosa and P. astreoides, whether hourly or seasonal, was highly sensitive to Ω arag. We believe this high sensitivity, however, is misleading, due to covariance between light and Ω arag, with the former being the strongest driver of calcification variability. For the seasonal data, we assessed the impact that the observed seasonal differences in temperature (4.0 °C), light (5.1 mol photons m−2 d−1), and Ω arag (0.16 units) would have on coral growth rates based on established relationships derived from laboratory studies and found that they could account for approximately 44, 52, and 5 %, respectively, of the observed seasonal change of 81 ± 14 mmol CaCO3 m−2 d−1. Using short-term light and dark incubations, we show how the covariance of light and Ω arag can lead to the false conclusion that calcification is more sensitive to Ω arag than it really is.

Calcium carbonate dissolution in the upper 1000 m of the eastern North Atlantic

AbstractRecent analyses suggest that considerable CaCO3 dissolution may occur in the upper water column of the ocean (< 1500 m). This study uses the distribution of particulate calcium from high‐resolution suspended matter sampling along the Climate Variability and Predictability/CO2 Repeat Hydrography A16N transect in 2003 to estimate CaCO3 dissolution in the top 1000 m of the North Atlantic. Dissolution rates were also approximated using changes in total alkalinity measurements along isopycnal surfaces. Water masses were found to be undersaturated with respect to aragonite at intermediate depths (400–1000 m) in the eastern tropical North Atlantic. The CaCO3 dissolution rate in this region is estimated to be 0.9 mmol CaCO3 m−2 d−1, indicating this region is a hotspot for upper water column CaCO3 dissolution compared to the Atlantic basin as a whole. Dissolution rates calculated from particulate calcium distributions outside of this region were significantly lower (0.2 mmol CaCO3 m−2 d−1) and are comparable to previous estimates of CaCO3 dissolution flux for the Atlantic Ocean. The magnitude of upper water column dissolution rates compared to measured surface ocean CaCO3 standing stocks suggests that biologically mediated CaCO3 dissolution may be occurring in the top 1000 m of the Atlantic.

Dynamics of seawater carbonate chemistry, production, and calcification of a coral reef flat, central Great Barrier Reef

Abstract. Ocean acidification is projected to shift coral reefs from a state of net accretion to one of net dissolution this century. Presently, our ability to predict global-scale changes to coral reef calcification is limited by insufficient data relating seawater carbonate chemistry parameters to in situ rates of reef calcification. Here, we investigate diel and seasonal trends in carbonate chemistry of the Davies Reef flat in the central Great Barrier Reef and relate these trends to benthic carbon fluxes by quantifying net ecosystem calcification (nec) and net community production (ncp). Results show that seawater carbonate chemistry of the Davies Reef flat is highly variable over both diel and seasonal cycles. pH (total scale) ranged from 7.92 to 8.17, pCO2 ranged from 272 to 542 μatm, and aragonite saturation state (Ωarag) ranged from 2.9 to 4.1. Diel cycles in carbonate chemistry were primarily driven by ncp, and warming explained 35% and 47% of the seasonal shifts in pCO2 and pH, respectively. Daytime ncp averaged 37 ± 19 mmol C m−2 h−1 in summer and 33 ± 13 mmol C m−2 h−1 in winter; nighttime ncp averaged −30 ± 25 and −7 ± 6 mmol C m−2 h−1 in summer and winter, respectively. Daytime nec averaged 11 ± 4 mmol CaCO3 m−2 h−1 in summer and 8 ± 3 mmol CaCO3 m−2 h−1 in winter, whereas nighttime nec averaged 2 ± 4 mmol and −1 ± 3 mmol CaCO3 m−2 h−1 in summer and winter, respectively. Net ecosystem calcification was highly sensitive to changes in Ωarag for both seasons, indicating that relatively small shifts in Ωarag may drive measurable shifts in calcification rates, and hence carbon budgets, of coral reefs throughout the year.

Dissolved inorganic carbon and total alkalinity of a Hawaiian fringing reef: chemical techniques for monitoring the effects of ocean acidification on coral reefs

There is an interest in developing approaches to “ecosystem-based” management for coral reefs. One aspect of ecosystem performance is to monitor carbon metabolism of whole communities. In an effort to explore robust techniques to monitor the metabolism of fringing reefs, especially considering the possible effects of ocean acidification, a yearlong study of the carbonate chemistry of a nearshore fringing reef in Hawaii was conducted. Diurnal changes in seawater carbonate chemistry were measured once a week in an algal-dominated and a coral-dominated reef flat on the Waimanalo fringing reef, Hawaii, from April of 2010 until May of 2011. Calculated rates of gross primary production (GPP) and net community calcification (G) were similar to previous estimates of community metabolism for other coral reefs (GPP 971 mmol C m−2 d−1; G 186 mmol CaCO3 m−2 d−1) and indicated that this reef was balanced in terms of organic metabolism, exhibited net calcification, and was a net source of CO2 to the atmosphere. Average slopes of total alkalinity versus dissolved inorganic carbon (TA–DIC slope) for the coral-dominated reef flat exhibited a greater calcification-to-net photosynthesis ratio than for the algal-dominated reef flat (coral slope vs. algal slope). Over the course of the time series, TA–DIC slopes remained significantly different between sites and were not correlated with diurnal averages in reef-water residence time or solar irradiance. These characteristic slopes for each reef flat reflect the relationship between carbon and carbonate community metabolism and can be used as a tool to monitor ecosystem function in response to ocean acidification.

High‐resolution carbon budgets on a Palau back‐reef modulated by interactions between hydrodynamics and reef metabolism

Diel trends in carbon chemistry and hydrodynamic regimes were measured on a coral‐dominated back‐reef community in the Republic of Palau, western Pacific. Observed diel ranges over 5 d were pH 7.92–8.09, partial pressure of carbon dioxide 33.4–52.7 Pa, measured total alkalinity 2080–2272 µmol kg−1, total dissolved inorganic carbon 1763–1939 µmol kg−1, aragonite saturation state 2.84–3.98, and calcite saturation state 4.44–5.67. The combination of reef metabolism and hydrodynamic regimes drives this variability. We report net community calcification (NCC) and net community production (NCP) rates of −20.4 (± 7.8) to 41.2 (± 37.7) mmol CaCO3 m−2 h−1 and 77.3 (± 95) to 64 (± 22) mmol C m−2 h−1, respectively. Using a control volume approach, we show that NCC and NCP rate estimates are quite sensitive to the effective control volume dimensions. At this site, tracking vertical mixing of water masses within the control volume shows that active water mixing is often confined to a region 2–3 m above the corals. Vertical carbon mass fluxes into and out of the benthic environment were unexpectedly large for the slow current flow rates observed, suggesting that coral morphology or reef rugosity may affect mass transport of carbon and nutrients. The ranges of NCC and NCP values highlight the need for additional field work on various reefs to tune and optimize the control volume approach to achieve its full potential for reef metabolism monitoring.

Seasonal coupling and de‐coupling of net calcification rates from coral reef metabolism and carbonate chemistry at Ningaloo Reef, Western Australia

Rates of net production, net calcification, and nutrient uptake were measured in a coral‐dominated reef flat community on Ningaloo Reef in northwestern Australia under seasonally minimum and maximum light levels. Daily integrated light decreased twofold while water temperatures remained relatively constant increasing by only 1°C on average from summer to winter. Rates of daily community gross primary production (GPP) were only 33% ± 9% higher in summer than in winter (1400 ± 70 versus 1050 ± 60 mmol C m−2 d−1), far less than the twofold seasonal changes reported for most shallow reef communities. Rates of daily community net calcification (Gnet) were not significantly different between seasons (190 ± 40 mmol CaCO3 m−2 d−1 in summer versus 200 ± 10 mmol CaCO3 m−2 d−1 in winter). The average rate of total nitrogen uptake (dissolved + particulate) was also not significantly different between summer and winter (8.3 ± 3.8 versus 6.6 ± 3.4 mmol N m−2 d−1, respectively), despite evidence of sporadically high nitrate uptake in both seasons. In summer, rates of hourly net calcification (gnet) were linearly correlated with diurnal changes in net production, pH, and aragonite saturation state (Ωar); and were mostly correlated with light except at mid‐day under heavy cloud cover. However, in winter,gnet was independent of diurnal changes in light, net production, pH, and Ωar indicating that the reef flat community had possibly reached a threshold above which rates of net calcification were insensitive to diurnal changes in their environment.

Quantifying the flux of CaCO3and organic carbon from the surface ocean using in situ measurements of O2, N2, pCO2, and pH

[1] Ocean acidification from anthropogenic CO2 has focused our attention on the importance of understanding the rates and mechanisms of CaCO3 formation so that changes can be monitored and feedbacks predicted. We present a method for determining the rate of CaCO3 production using in situ measureme nts of fCO2 and pH in surface waters of the eastern subarctic Pacific Ocean. These quantities were determined on a surface mooring every 3 h for a period of about 9 months in 2007 at Ocean Station Papa (50°N, 145°W). We use the data in a simple surface ocean, mass balance model of dissolved inorganic carbon (DIC) and alkalinity (Alk) to constrain the CaCO3: organic carbon (OC) production ratio to be approximately 0.5. A CaCO3 production rate of 8 mmol CaCO3 m−2 d−1 in the summer of 2007 (1.2 mol m−2 yr−1) is derived by combining the CaCO3: OC ratio with the a net organic carbon production rate (2.5 mol C m−2 yr−1) determined from in situ measurements of oxygen and nitrogen gas concentrations measured on the same mooring (Emerson and Stump, 2010). Carbonate chemistry data from a meridional hydrographic section in this area in 2008 indicate that isopycnal surfaces that outcrop in the winter in the subarctic Pacific and deepen southward into the subtropics are a much stronger source for alkalinity than vertical mixing. This pathway has a high enough Alk:DIC ratio to support the CaCO3:OC production rate implied by the fCO2 and pH data.

Net Loss of CaCO<sub>3</sub> from a subtropical calcifying community due to seawater acidification: mesocosm-scale experimental evidence

Abstract. Acidification of seawater owing to oceanic uptake of atmospheric CO2 originating from human activities such as burning of fossil fuels and land-use changes has raised serious concerns regarding its adverse effects on corals and calcifying communities. Here we demonstrate a net loss of calcium carbonate (CaCO3) material as a result of decreased calcification and increased carbonate dissolution from replicated subtropical coral reef communities (n=3) incubated in continuous-flow mesocosms subject to future seawater conditions. The calcifying community was dominated by the coral Montipora capitata. Daily average community calcification or Net Ecosystem Calcification (NEC=CaCO3 production – dissolution) was positive at 3.3 mmol CaCO3 m−2 h−1 under ambient seawater pCO2 conditions as opposed to negative at −0.04 mmol CaCO3 m−2 h−1 under seawater conditions of double the ambient pCO2. These experimental results provide support for the conclusion that some net calcifying communities could become subject to net dissolution in response to anthropogenic ocean acidification within this century. Nevertheless, individual corals remained healthy, actively calcified (albeit slower than at present rates), and deposited significant amounts of CaCO3 under the prevailing experimental seawater conditions of elevated pCO2.

Dissolution of Carbonate Sediments Under Rising pCO2 and Ocean Acidification: Observations from Devil’s Hole, Bermuda

Rising atmospheric pCO2 and ocean acidification originating from human activities could result in increased dissolution of metastable carbonate minerals in shallow-water marine sediments. In the present study, in situ dissolution of carbonate sedimentary particles in Devil’s Hole, Bermuda, was observed during summer when thermally driven density stratification restricted mixing between the bottom water and the surface mixed layer and microbial decomposition of organic matter in the subthermocline layer produced pCO2 levels similar to or higher than those levels anticipated by the end of the 21st century. Trends in both seawater chemistry and the composition of sediments in Devil’s Hole indicate that Mg-calcite minerals are subject to selective dissolution under conditions of elevated pCO2. The derived rates of dissolution based on observed changes in excess alkalinity and estimates of vertical eddy diffusion ranged from 0.2 mmol to 0.8 mmol CaCO3 m−2 h−1. On a yearly basis, this range corresponds to 175–701 g CaCO3 m−2 year−1; the latter rate is close to 50% of the estimate of the current average global coral reef calcification rate of about 1,500 g CaCO3 m−2 year−1. Considering a reduction in marine calcification of 40% by the year 2100, or 90% by 2300, as a result of surface ocean acidification, the combination of high rates of carbonate dissolution and reduced rates of calcification implies that coral reefs and other carbonate sediment environments within the 21st and following centuries could be subject to a net loss in carbonate material as a result of increasing pCO2 arising from burning of fossil fuels.

Community metabolism in temperate maerl beds. I. Carbon and carbonate fluxes

Maerl community respiration, photosynthesis and calcification were measured season- ally in the Bay of Brest (France). The dynamics of oxygen, carbon and carbonate fluxes at the water-sediment interface were assessed using benthic chambers. Community respiration (CR) fluc- tuated in accordance with the seasonal changes in water temperature, from 1.5 mmol C m -2 h -1 in winter to 8.7 mmol C m -2 h -1 in summer. Mean gross community production (GCP) varied signifi- cantly among seasons, according to incident irradiance and temperature, from 3.4 mmol C m -2 h -1 in winter to 12.7 mmol C m -2 h -1 in summer. Mean annual Pmax for the P-E curve was estimated to 13.3 mmol C m -2 h -1 . Carbonate precipitation only occurred during light incubations and varied sea- sonally from 0.7 mmol CaCO3 m -2 h -1 in winter to 4.2 mmol CaCO3 m -2 h -1 in summer. Mean annual Pmax was 3.2 mmol CaCO3 m -2 h -1 . Annual CR was estimated to 407.4 g C m -2 yr -1 , and GCP, to 240.9 g C m -2 yr -1 . Maerl communities are, therefore, heterotrophic systems (GCP:CR = 0.6), and are a source of CO2 for surrounding environments. In addition, CO2 released by calcification averaged 39.2 g C m -2 yr -1 . Maerl community annual carbonate production was estimated to 486.7 g CaCO3 m -2 yr -1 ; they are therefore one of the most important carbonate producers in shallow coastal waters.

Community primary production and calcification in a NW Mediterranean ecosystem dominated by calcareous macroalgae

MEPS Marine Ecology Progress Series Contact the journal Facebook Twitter RSS Mailing List Subscribe to our mailing list via Mailchimp HomeLatest VolumeAbout the JournalEditorsTheme Sections MEPS 334:37-45 (2007) - doi:10.3354/meps334037 Community primary production and calcification in a NW Mediterranean ecosystem dominated by calcareous macroalgae Nathaniel Bensoussan1,*, Jean-Pierre Gattuso2 1Laboratoire Diversité, évolution et écologie fonctionnelle marine, CNRS—Université de la Méditerranée, Centre d’Océanologie de Marseille, Station Marine d’Endoume, rue Batterie des Lions, 13007 Marseille, France 2Laboratoire d’Océanographie de Villefranche, CNRS—Université de Paris 6, BP 28, 06234 Villefranche-sur-mer Cedex, France *Email: nathaniel.bensoussan@univmed.fr ABSTRACT: The community metabolism of a shallow infralittoral ecosystem dominated by the calcareous macroalgae Corallina elongata was investigated in Marseilles (NW Mediterranean), by monitoring hourly changes of seawater pH and total alkalinity over 6 d in February 2000. Fair weather conditions prevailed over the study period as indicated by oceanographic (temperature, salinity, and current velocity and direction) and meteorological variables, which validated the standing water hypothesis. This temperate ecosystem exhibited high community gross primary production (GPP = 519 ± 106 mmol C m–2 d–1, n = 6) and also supported high rates of community respiration (R). As a result, the system was slightly autotrophic (net community production, NCP = 20 mmol C m–2 d–1), with a GPP/R ratio of 1.06. NCP exhibited circadian variations with 2- to 3-fold changes in community respiration, both in the light and in the dark. Rates of net community calcification also exhibited circadian variations, with positive rates (up to 24 mmol CaCO3 m–2 h–1) for irradiance values >300 W m–2 (about 1380 µmol photon m–2 s–1). Below this irradiance threshold, net community dissolution prevailed. Daily net calcification (G) was on average 8 mmol CaCO3 m–2 d–1. CO2 fluxes generated by primary production, respiration, and calcification suggest that the study site was a potential atmospheric CO2 sink of 15 mmol CO2 m–2 d–1 at the time of measurement. KEY WORDS: Ecosystem metabolism · Primary production · Respiration · Calcification · Calcareous macroalgae · Corallina elongata · pH · Total alkalinity · TA Full text in pdf format PreviousNextExport citation RSS - Facebook - Tweet - linkedIn Cited by Published in MEPS Vol. 334. Online publication date: March 26, 2007 Print ISSN: 0171-8630; Online ISSN: 1616-1599 Copyright © 2007 Inter-Research.