Changes In Carbonate Chemistry Research Articles

Calcification in sea urchin larvae is associated with low metabolic costs.

The energetic costs to generate calcium carbonate skeletons and shells in marine organisms remain largely speculative due to the scarcity of empirical data. However, this information is critical to estimate energetic limitations of marine calcifiers that can explain their sensitivities to changes in sea water carbonate chemistry in past, present and future marine systems. The cost of calcification was evaluated using larval stages of the purple sea urchin, Strongylocentrotus purpuratus. We developed a skeleton re-mineralization assay, in which the skeleton was dissolved in live larvae followed by a re-mineralization over a few days. During skeleton re-mineralization, energetic costs were estimated through the measurement of key metabolic parameters including whole animal metabolic rates, citrate synthase (CS) enzyme activities and mRNA expression as well as mitochondrial densities in the calcifying primary mesenchyme cells (PMCs). Minor increases in a CS activity and a 10-15% increase in mitochondrial densities in PMCs were observed in re-mineralizing larvae as compared to control larvae. Re-mineralization under three different pH conditions (pH 8.1, pH 7.6 and pH 7.1) decreased with decreasing pH accompanied by pronounced increases in CS expression levels and increased mitochondrial densities in PMCs at pH 7.6. Despite a prominent increase in mitochondrial density of primary mesenchyme cells, particularly in the calcifying cohort of this cell type, this work demonstrated a low overall metabolic response to increased mineralization rates on the whole animal level under both, high and low pH conditions. We conclude that calcification in sea urchin larvae is compromised under low pH conditions, associated with low energetic efforts to fuel compensatory processes.

Paired X‐Ray Micro CT Scanning and Individual Foraminifera Isotopic Analysis Reveal (De)coupled Changes in Carbonate Preservation and Temperature

AbstractThe composition and preservation state of biogenic carbonate archives, such as foraminiferal tests, record ocean chemistry during the lifetime of the organism and post‐depositional changes in ambient conditions via carbonate compensation. Depending upon the specific paleoclimate proxy, post‐depositional processes, including dissolution, may alter original paleoenvironmental signals captured by the foraminifer's test composition. Accordingly, quantifying dissolution independent of geochemical measurements can improve proxy interpretation. Developing independent tools may also be useful for investigating whether changes in paleoclimatic conditions are associated with changes in seawater carbonate chemistry. Such approaches can be improved further if they are applied to individual foraminiferal tests, as specimen‐to‐specimen differences can record higher‐frequency environmental changes compared to conventional bulk‐scale analyses. Here, we combine individual foraminiferal carbon and oxygen isotopic analyses (IFA) with X‐ray MicroCT Scanning to generate paired analyses of test density (a proxy for the extent of post‐depositional dissolution) and isotopic composition. As a proof‐of‐concept application of this approach, we analyze Globigerina bulloides tests from both coretop and latest Miocene/earliest Pliocene‐aged sediment from Ocean Drilling Project (ODP) Site 1088 (Agulhas Ridge). Our measurements and mixing model calculations show that within‐population differences in carbon and oxygen isotopic ratios are largely independent of dissolution extent. By comparing population averages from coretop and downcore sediments, we find that lower oxygen isotopic ratios (likely driven by higher calcification temperatures) are associated with greater extents of dissolution at ODP Site 1088. We interpret this finding to reflect coupled changes in carbonate chemistry and climatic conditions over million‐year timescales.

Pile burns as a proxy for high severity wildfire impacts on soil microbiomes

Wildfires in the western US are increasing in frequency, size, and severity. These disturbances alter soil microbiome structure and function, with greater fire severity leading to more pronounced impacts to bacterial, archaeal, and fungal communities. These changes have implications for the provisioning of microbially-mediated ecosystem services (e.g., carbon sequestration, clean water supplies) typically associated with forested watersheds. Challenges in sampling wildfire-impacted areas immediately post-burn have limited our assessment of short-term (i.e., days to weeks) changes in the soil microbiome and understanding of how microbial populations may influence post-fire biogeochemistry and ecosystem recovery. The identification of potential high severity wildfire proxies may help address some of these knowledge gaps. One potential proxy is pile burns scars, which are produced from a set of common techniques for fuel disposal and site preparation in conifer forests throughout the western US and beyond. We sampled depth-resolved layers from fire-impacted soil and combusted litter and woody materials in a series of recent pile burn scars near West Yellowstone, Montana and nearby unburned mineral soil controls to assess whether the pile burn scars exhibited microbial signatures characteristic of forest soils impacted by recent high severity wildfire. Changes in soil carbon and nitrogen chemistry and patterns of microbial alpha and beta diversity broadly aligned with those observed following wildfire, particularly the enrichment of so-called ‘pyrophilous’ taxa. Furthermore, many of the taxa enriched in burned soils likely encoded putative traits that benefit microorganisms colonizing these environments, such as the potential for fast growth or utilization of pyrogenic carbon substrates. We suggest that pile burn scars may represent a useful proxy along the experimental gradient from muffle furnace or pyrocosm studies to largescale prescribed burns in the field to advance understanding of the soil (and related layers, like ash) microbiome following high severity wildfires, particularly when coupled with experimental manipulation. Finally, we discuss existing research gaps that experimentally manipulated pile burns could be utilized to address.

Shellfish CO2 excretion is modulated by seawater carbonate chemistry but largely independent of pCO2.

Four species of shellfish, blue mussel (Mytilus galloprovincialis), Pacific abalone (Haliotis discus hannai), zhikong scallops (Chlamys farreri), and Pacific oyster (Crassostrea gigas), were exposed to decoupled carbonate system variables to investigate the impacts of different seawater carbonate parameters on the CO2 excretion process of mariculture shellfish. Six experimental groups with two levels of seawater pH (pH 8.1 and pH 7.7) and three levels of total alkalinity (TA = 1000, 2300, and 3600μmol/kg, respectively) were established, while pH 8.1 and TA = 2300μmol/kg was taken as control. Results showed that the CO2 excretion rates of these tested shellfish were significantly affected by the change in carbonate chemistry (P < 0.05). At the same TA level, animals incubated in the acidified group (pH 7.7) had a lower CO2 excretion rate than those in the control group (pH 8.1). In comparison, at the same pH level, the CO2 excretion rate increased when seawater TA level was elevated. No significant correlation between the CO2 excretion rate and seawater pCO2 levels (P > 0.05) was found; however, a significant correlation (P < 0.05) between CO2 excretion rate and TA-DIC (the difference between total alkalinity and dissolved inorganic carbon) was observed. Blue mussel has a significantly higher CO2 excretion rate than the other three species in the CO2 excretions per unit mass of soft parts, with no significant difference observed among these three species. However, in terms of CO2 excretion rate per unit mass of gills, abalone has the highest CO2 excretion rate, while significant differences were found between each species. Our studies indicate that the CO2 buffering capacity impacts the CO2 excretion rate of four shellfish species largely independent of pCO2. Since CO2 excretion is related to acid-base balancing, the results imply that the effects of other carbonate parameters, particularly the CO2 buffering capacity, should be studied to fully understand the mechanism of how acidification affects shellfish. Besides, the species difference in gill to soft parts proportion may contribute to the species difference in responding to ocean acidification.

Patterns of carbonate chemistry in mangroves of the Northern Persian Gulf

The mangroves located in the Northern Persian Gulf are reeling from anthropogenic pressures including from intense industrial activities (Pars Special Economic Energy Zone-PSEEZ). Given the unique geographical location of these mangroves, understanding the initial basis of seawater carbonate chemistry is key to link with global patterns of coastal ocean carbonate dynamics. In this study, water samples were collected from pre-designated stations representing the mangrove forest and nearshore water namely Nayband, Mel-e-Gonzeh and Bardestan of the Persian Gulf in September of 2016. Based on extensive carbonate chemistry measurements, the results show that the pCO2 at the Nayband site (13217.9±5841.5 µatm) was significantly higher than the other two sites (Mel-e-Gonzeh: 416.4±49.3 µatm and Bardestan: 294.3±95.0 µatm) while pH (6.92±0.18) was significantly lower than the two other sites (Mel-e-Gonzeh: 8.18±0.02, Bardestan: 8.26±0.04). The observed increase of pCO2 and decrease of surface water pH at the Nayband site compared to other two sites may have due to the emission of CO2 originating from oil and gas refining facilities located PSEEZ. Moreover, surface water in Nayband was undersaturated with respect to aragonite (Ωarg<1) and supersaturated (Ωarg>1) in case of the Mel-e-Gonzeh and Bardestan sites. This study although preliminary provides much-needed baseline information to address issues of changing carbonate chemistry and can help towards understanding the basis of coastal ocean acidification.

Time-dependent Changes in Shrimp Armor and Escape Kinematics under Ocean Acidification and Warming.

Pandalid shrimp use morphological and behavioral defenses against their numerous fish and invertebrate predators. Their rapid tail-flip escape and rigid exoskeleton armor may be sensitive to changes in ocean temperature and carbon chemistry in ways that alter their efficacy and impact mortality. Here we tested the hypothesis that ocean warming and acidification conditions affect the antipredator defenses of Pandalus gurneyi. To test this hypothesis, we exposed shrimp to a combination of pH (8.0, 7.7, 7.5) and temperature (13°C, 17°C) treatments and assessed their tail-flip escape and exoskeleton armor after short-term (2 weeks) and medium-term (3 months) exposure. Results revealed complex effects on escape kinematics, with changes in different variables explained by either pH, temperature, and/or their interaction; decreased pH, for instance, primarily explains reduced acceleration while cold temperature explains increased flexion duration. Carapace mineral content (Ca and Mg) was unaffected, but warmer temperatures primarily drove enhanced mechanical properties (increased hardness and stiffness). No effects were observed in the stiffness and strength of the rostrum. Furthermore, most of the observed effects were temporary, as they occurred after short-term exposure (2 weeks), but disappeared after longer exposure (3 months). This demonstrates that P. gurneyi defenses are affected by short-term exposure to temperature and pH variations; however, they can acclimate to these conditions over time. Nonetheless, changes in the tail-flip escape kinematics may be disadvantageous when trying to flee predators and the enhanced exoskeleton armor could make them more resistant to predation during short periods of environmental change.

Quantifying the combined impacts of anthropogenic CO2 emissions and watershed alteration on estuary acidification at biologically-relevant time scales: a case study from Tillamook Bay, OR, USA.

The impacts of ocean acidification (OA) on coastal water quality have been subject to intensive research in the past decade, but how emissions-driven OA combines with human modifications of coastal river inputs to affect estuarine acidification dynamics is less well understood. This study presents a methodology for quantifying the synergistic water quality impacts of OA and riverine acidification on biologically-relevant timescales through a case study from a small, temperate estuary influenced by coastal upwelling and watershed development. We characterized the dynamics and drivers of carbonate chemistry in Tillamook Bay, OR (USA), along with its coastal ocean and riverine end-members, through a series of synoptic samplings and continuous water quality monitoring from July 2017 to July 2018. Synoptic river sampling showed acidification and increased content in areas with higher proportions of watershed anthropogenic land use. We propagated the impacts of 1). the observed riverine acidification, and 2). modeled OA changes to incoming coastal ocean waters across the full estuarine salinity spectrum and quantified changes in estuarine carbonate chemistry at a 15-minute temporal resolution. The largest magnitude of acidification (-1.4 units) was found in oligo- and mesohaline portions of the estuary due to the poor buffering characteristics of these waters, and was primarily driven by acidified riverine inputs. Despite this, emissions-driven OA is responsible for over 94% of anthropogenic carbon loading to Tillamook Bay and the dominant driver of acidification across most of the estuary due to its large tidal prism and relatively small river discharges. This dominance of ocean-sourced anthropogenic carbon challenges the efficacy of local management actions to ameliorate estuarine acidification impacts. Despite the relatively large acidification effects experienced in Tillamook Bay (-0.16 to -0.23 units) as compared with typical open ocean change (approximately -0.1 units), observations of estuarine would meet existing state standards for . Our analytical framework addresses pressing needs for water quality assessment and coastal resilience strategies to differentiate the impacts of anthropogenic acidification from natural variability in dynamic estuarine systems.

Observing Temporally Varying Synoptic‐Scale Total Alkalinity and Dissolved Inorganic Carbon in the Arctic Ocean

AbstractThe long‐term absorption by the oceans of atmospheric carbon dioxide is leading to the slow decline of ocean pH, a process termed ocean acidification (OA). The Arctic is a challenging region to gather enough data to examine the changes in carbonate chemistry over sufficient scales. However, algorithms that calculate carbonate chemistry parameters from more frequently measured parameters, such as temperature and salinity, can be used to fill in data gaps. Here, these published algorithms were evaluated against in situ measurements using different data input types (data from satellites or in situ re‐analysis climatologies) across the Arctic Ocean. With the lowest uncertainties in the Atlantic influenced Seas (AiS), where re‐analysis inputs achieved total alkalinity estimates with Root Mean Squared Deviation (RMSD) of 21 μmol kg−1 and a bias of 2 μmol kg−1 (n = 162) and dissolved inorganic carbon RMSD of 24 μmol kg−1 and bias of −14 μmol kg−1 (n = 262). AiS results using satellite observation inputs show similar bias but larger RMSD, although due to the shorter time span of available satellite observations, more contemporary in situ data would provide further assessment and improvement. Synoptic‐scale observations of surface water carbonate conditions in the Arctic are now possible to monitor OA, but targeted in situ data collection is needed to enable the full exploitation of satellite observation‐based approaches.

Assessing seasonal and interannual changes in carbonate chemistry across two time-series sites in the North Western Mediterranean Sea

Sustained time-series measurements are crucial to understand changes in oceanic carbonate chemistry. In the North Western Mediterranean Sea, the temporal evolution of the carbonate system is here investigated based on two 10-year time-series (between January 2010 and December 2019) of monthly carbonate parameters measurements at two sampling sites in the Ligurian Sea (ANTARES and DYFAMED). At seasonal timescale, the seawater partial pressure of CO2 (pCO2) within the mixed layer is mostly driven by temperature at both sites, and biological processes as stated by the observed relationships between total inorganic carbon (CT), nitrate and temperature. This study suggests also that mixing and water masses advection could play a role in modulating the CT content. At decadal timescale, significant changes in ocean chemistry are observed with increasing trends in CT (+3.2 ± 0.9 µmol.kg−1.a−1 – ANTARES; +1.6 ± 0.8 µmol.kg−1.a−1 – DYFAMED), associated with increasing pCO2 trends and decreasing trends in pH. The magnitude of the increasing trend in CT at DYFAMED is consistent with the increase in atmospheric pCO2 and the anthropogenic carbon transport of water originating from the Atlantic Ocean, while the higher trends observed at the ANTARES site could be related to the hydrological variability induced by the variability of the Northern Current.

Warming, acidification, and calcification feedback during the first hyperthermal of the Cenozoic—The Latest Danian Event

Abstract The Latest Danian Event (LDE; ca. 62.15 Ma) is a major double-spiked eccentricity-driven transient warming event and carbon cycle perturbation (hyperthermal) in the early Paleocene, which has received significantly less attention compared to the larger events of the late Paleocene–early Eocene. A better understanding of the nature of the LDE may broaden our understanding of hyperthermals more generally and improve our knowledge of Earth system responses to extreme climate states. We present planktic and benthic foraminiferal Mg/Ca and B/Ca records that shed new light on changes in South Atlantic temperature and carbonate chemistry during the LDE. Our planktic Mg/Ca record reveals a pulsed increase in sea-surface temperature of at least ~1.5 °C during the older carbon isotope excursion, and ~0.5 °C during the younger isotope excursion. We observe drops in planktic and benthic B/Ca, synchronous with pronounced negative excursions in benthic δ13C, which suggest a shift in the carbonate system toward more acidic, dissolved inorganic carbon–rich conditions, in both the surface and deep ocean. Conditions remained more acidic following the LDE, which we suggest may be linked to an enhanced ocean alkalinity sink due to changes in the makeup of planktic calcifiers, hinting at a novel feedback between calcifier ecology and ocean-atmosphere CO2.

Globally enhanced calcification across the coccolithophore Gephyrocapsa complex during the mid-Brunhes interval

Evolutionary or adaptative changes in Noelaerhabdaceae coccolithophores occurred in parallel with major changes in carbonate export and burial during scenarios of low orbital eccentricity, with a ∼400 kyr recurrence, during the Pleistocene. Coeval with these conditions of enhanced proliferation, here we report that the calcification of specimens was enhanced at a global scale and across multiple species or morphotypes within the Gephyrocapsa complex during the Mid-Brunhes (MB) interval. This acme of increased production of organic and inorganic carbon by Gephyrocapsa, suggests that such global changes may originate from a common driver. Increased seawater alkalinity, with an appropriately long residence time, is proposed as environmental trigger on the selection of a wide variety of highly calcified and prolific Gephyrocapsa taxa. This new perspective highlights the role of orbital forcing in phytoplankton evolution or adaptation, via a global environmental driver in the form of seawater carbon chemistry. Our results fit with earlier proposals appealing for an intensified biological pump and respiration dissolution during this interval. We hypothesize that the Gephyrocapsa acme may play a double-edged role, by increasing shallow respiration dissolution rates, limiting the removal of alkalinity by burial, which may help to recycle alkalinity and maintain constant levels at the ∼400 kyr scale. This idea suggests the potential capacity of the Noelaerhabdaceae coccolithophore acmes to modify the typical behaviour of carbonate compensation in the ocean and that the changes in coccolithophore calcification may be indicative of changes in ocean carbonate chemistry and the operation of the global carbon cycle in the past.

From reproductive behaviour to responses to predators: Ocean acidification does not impact the behaviour of an herbivorous marine gastropod

Ocean acidification (OA), which reduces ocean pH and leads to substantial changes in seawater carbonate chemistry, may strongly impact organisms, especially those with carbonate skeletons. In marine molluscs, while the physiological effects of OA are well known, with a reduction of growth and shell calcification, there are few studies on behavioural effects. A large marine gastropod, Haliotis tuberculata, was exposed to ambient (pHT 8.0) or low pH (pHT 7.7) during a 5-month experiment. Because animal fitness can be affected through various behavioural changes, a broad spectrum of behavioural parameters was investigated, including situations involving no stress, responses to predators, righting to evaluate indirectly the level of energy reserves, and finally, reproductive behaviour. In addition, we measured the expression profile of the GABA A-like and serotonin receptor genes, often described as central neuromodulators of sensory performance and behaviour and known to be affected by OA in molluscs. No significant effect of low pH as compared to ambient pH was observed on abalone behaviour for any of these behavioural traits or gene expressions after either one week or several months of exposure to OA. The significance tests were corroborated by estimating the size of pH effects. The behaviour of this mollusc appears not to be affected by pH decrease expected by the end of the century, suggesting some resilience of the species to OA at the adult stage. This is probably related to the ecological niche of this abalone, where important pH variations can be observed at tidal, diurnal or seasonal scales.

The combined effect of pH and dissolved inorganic carbon concentrations on the physiology of plastidic ciliate Mesodinium rubrum and its cryptophyte prey

Ocean acidification is caused by rising atmospheric partial pressure of CO2 (pCO2) and involves a lowering of pH combined with increased concentrations of CO2 and dissolved in organic carbon in ocean waters. Many studies investigated the consequences of these combined changes on marine phytoplankton, yet only few attempted to separate the effects of decreased pH and increased pCO2. Moreover, studies typically target photoautotrophic phytoplankton, while little is known of plastidic protists that depend on the ingestion of plastids from their prey. Therefore, we studied the separate and interactive effects of pH and DIC levels on the plastidic ciliate Mesodinium rubrum, which is known to form red tides in coastal waters worldwide. Also, we tested the effects on their prey, which typically are cryptophytes belonging to the Teleaulax/Plagioslemis/Geminigera species complex. These cryptophytes not only serve as food for the ciliate, but also as a supplier of chloroplasts and prey nuclei. We exposed M. rubrum and the two cryptophyte species, T. acuta, T. amphioxeia to different pH (6.8 - 8) and DIC levels (∼ 6.5 - 26 mg C L-1) and assessed their growth and photosynthetic rates, and cellular chlorophyll a and elemental contents. Our findings did not show consistent significant effects across the ranges in pH and/or DIC, except for M. rubrum, for which growth was negatively affected only by the lowest pH of 6.8 combined with lower DIC concentrations. It thus seems that M. rubrum is largely resilient to changes in pH and DIC, and its blooms may not be strongly impacted by the changes in ocean carbonate chemistry projected for the end of the 21st century.

Prolonged deep-ocean carbonate chemistry recovery after the Paleocene-Eocene Thermal Maximum

The Paleocene-Eocene Thermal Maximum (PETM) is a hyperthermal event at ∼56 Ma ago, caused by rapid and massive carbon releases into the ocean-atmosphere system. Currently, the PETM ocean acidification is mainly quantified in the surface ocean. By contrast, PETM carbonate chemistry changes of the deep ocean, a larger carbon reservoir, are largely qualitatively constrained by sedimentary calcium carbonate contents (%CaCO3). Here, we revisit a previously proposed method for quantifying Early Cenozoic deep-water carbonate chemistry, using boron to calcium ratios (B/Ca) in extinct benthic foraminifera Nuttallides truempyi (Brown et al., 2011). We show that calibrating core-top B/Ca in the extant relative of N. truempyi against deep-water calcite saturation degree (Ω, Ω = [CO32−] /[CO32−]saturated), rather than calcite saturation state (Δ[CO32−], Δ[CO32−] = [CO32−] - [CO32−]saturated) as originally proposed better reflects Early Cenozoic carbonate chemistry changes. Furthermore, we provide multiple deep-water Ω reconstructions paired with benthic foraminiferal carbon isotopes during the PETM. At two sites, deep-water Ω recovered synchronously with carbon isotopes but lagged the sedimentary %CaCO3 rebound, indicating a slower post-PETM deep-water Ω recovery than previously thought. This may imply that during the PETM recovery phase, carbon could have been injected into the ocean-atmosphere system, despite net carbon loss, over a prolonged period after the initial release. If so, during this period, carbon removal from the ocean via calcite burial on the seafloor in response to enhanced silicate weathering may be weakened, suggesting that more carbon was sequestered via other processes such as those related to organic carbon burial.

Constraining oceanic carbonate chemistry evolution during the Cretaceous-Paleogene transition: Combined benthic and planktonic calcium isotope records from the equatorial Pacific Ocean

The Mesozoic-Cenozoic transition is a period of biogeochemical cycle perturbations. The strongest of them is the Cretaceous-Paleogene boundary (K-Pg) crisis, characterized by one of the most important extinctions of planktonic marine calcifiers in Earth's history. One of the primary drivers of this biocalcification crisis is thought to be the increase in atmospheric CO2 concentration and ocean acidification triggered by the Chicxulub Impact, and/or Deccan volcanism. Because it reflects changes of the calcium cycle and/or depends on parameters of the carbonate system, the Ca isotope composition of carbonate minerals precipitated from seawater (δ44/40Ca) offers the potential to reconstruct some of the environmental changes that occurred. Here we present new high-resolution planktonic and benthic foraminiferal δ44/40Ca, δ18O, δ13C, and Sr/Ca records across the K-Pg transition from Shatsky rise (Leg 198; ODP Site 1209, Hole C). The δ44/40Ca record displays a succession of rapid shifts of ca. −0.4‰ across the K-Pg transition. They are similar though not identical between the planktonic and benthic records. These shifts took place on a timescale significantly shorter than the residence time of Ca in the oceans and are therefore unlikely to result from global disequilibrium in the oceanic Ca budget. Instead, changes in the fractionation factor between carbonate minerals and seawater in response to changes in precipitation rates may explain the observed δ44/40Ca and Sr/Ca record. The benthic and planktonic δ44/40Ca records show a late Maastrichtian and an early Danian negative excursions best explained by a succession of episodes of ocean alkalinity increase related to increased continental weathering caused by CO2 emissions from Deccan volcanism and the aftermath of the K-Pg biocalcification crisis. Carbonate compensation via carbonate sediment dissolution, biological carbonate compensation via reduction of biocalcification, and/or an increase in continental weathering must have occurred to offset the excess CO2, ultimately resulting in rapid changes in ocean carbonate chemistry, in combination with reduced surface alkalinity export in response to the early Paleogene planktonic biomineralization crisis.

Response of ocean acidification to atmospheric carbon dioxide removal

Artificial CO2 removal from the atmosphere (also referred to as negative CO2 emissions) has been proposed as a potential means to counteract anthropogenic climate change. Here we use an Earth system model to examine the response of ocean acidification to idealized atmospheric CO2 removal scenarios. In our simulations, atmospheric CO2 is assumed to increase at a rate of 1% per year to four times its pre-industrial value and then decreases to the pre-industrial level at a rate of 0.5%, 1%, 2% per year, respectively. Our results show that the annual mean state of surface ocean carbonate chemistry fields including hydrogen ion concentration ([H+]), pH and aragonite saturation state respond quickly to removal of atmospheric CO2. However, the change of seasonal cycle in carbonate chemistry lags behind the decline in atmospheric CO2. When CO2 returns to the pre-industrial level, over some parts of the ocean, relative to the pre-industrial state, the seasonal amplitude of carbonate chemistry fields is substantially larger. Simulation results also show that changes in deep ocean carbonate chemistry substantially lag behind atmospheric CO2 change. When CO2 returns to its pre-industrial value, the whole-ocean acidity measured by [H+] is 15%-18% larger than the pre-industrial level, depending on the rate of CO2 decrease. Our study demonstrates that even if atmospheric CO2 can be lowered in the future as a result of net negative CO2 emissions, the recovery of some aspects of ocean acidification would take decades to centuries, which would have important implications for the resilience of marine ecosystems.

Comparison of the carbon cycle and climate response to artificial ocean alkalinization and solar radiation modification

Carbon dioxide removal and solar radiation modification (SRM) are two classes of proposed climate intervention methods. A thorough understanding of climate system response to these methods calls for a good understanding of the carbon cycle response. In this study, we used an Earth system model to examine the response of global climate and carbon cycle to artificial ocean alkalinization (AOA), a method of CO2 removal, and reduction in solar irradiance that represents the overall effect of solar radiation modification. In our simulations, AOA is applied uniformly over the global ice-free ocean under the RCP8.5 scenario to bring down atmospheric CO2 to the level of RCP4.5, and SRM is applied uniformly over the globe under the RCP8.5 scenario to bring down global mean surface temperature to the level of RCP4.5. Our simulations show that with the same goal of temperature stabilization, AOA and SRM cause fundamentally different perturbations of the ocean and land carbon cycle. By the end of the 21st century, relative to the simulation of RCP8.5, AOA-induced changes in ocean carbonate chemistry enhances global oceanic CO2 uptake by 983 PgC and increases global mean surface ocean pH by 0.42. Meanwhile, AOA reduces land CO2 uptake by 79 PgC and reduces atmospheric CO2 concentration by 426 × 10−6. By contrast, relative to the simulation of RCP8.5, SRM has a minor effect on the oceanic CO2 uptake and ocean acidification. SRM-induced cooling enhances land CO2 uptake by 140 PgC and reduces atmospheric CO2 concentration by 63 × 10−6. A sudden termination of SRM causes a rate of temperature change that is much larger than that of RCP8.5. A sudden termination of AOA causes a rate of temperature change that is comparable to that of RCP8.5 and a rate of ocean acidification that is much larger than that of RCP8.5.

Drivers of Marine CO2‐Carbonate Chemistry in the Northern Antarctic Peninsula

AbstractThe Bransfield Strait is a climate change hotspot at the tip of the northern Antarctic Peninsula (NAP). The region is marked by a mixture of relatively warm waters from the Bellingshausen Sea with cold shelf waters from the Weddell Sea. Additionally, its deep central basin (&gt;800 m) preserves seawater properties from the north‐western Weddell Sea continental shelf. This study assessed long‐term changes in carbonate chemistry in the Bransfield Strait and found that the hydrographic setting (i.e., a mixture between modified‐Circumpolar Deep Water with Dense Shelf Water [DSW]) drives temporal variability of carbonate parameters. The western basin has experienced decreases in pH (seawater scale) over the last three decades (1996–2019), varying from −0.003 to −0.017 pH units yr−1, while Ωar decreased from −0.01 to −0.07 yr−1 throughout the water column. The central basin was characterized by a high contribution of DSW with high carbon dioxide (CO2) content and the decomposition of organic matter produced and transported into its deep layer. With lower variability for all carbonate system variables, the eastern basin was likely regulated by internal mixing. Overall, the entire strait is almost reaching a CO2‐saturated condition, highlighting how sensitive subpolar regions are to the effects of human‐induced climate change.

INTERACTION OF CO2 AND LIGHT AVAILABILITY ON PHOTOPHYSIOLOGY OF TROPICAL COCCOLITOPHORIDS (EMILIANIA HUXLEYI, GEPHYROCAPSA OCEANICA, AND OCHOSPHAERA SP.)

The study to examine the calcification rate, adaptation, and the biotic response of three tropical coccolithophorids (Emiliania huxleyi, Gephyrocapsa oceanica, and Ochosphaera sp) to changes in CO2 concentration. Three selected calcifying coccolitophorids were grown at batch culture with CO2 system at two levels of CO2 (385 and 1000 ppm) and two light dark periods. The parameters measured and calculation including growth rate, particulate organic carbon content, particulate inorganic carbon content, chlorophyll a, cell size, photosynthetic, organic, inorganic carbon production, photosynthesis, and calcification rate. The results showed that there was a different response to carbonate chemistry changes and dark and light periods in any of the analyzed parameters. The growth rate of three selected calcifying microalgae tested was decreasing significantly at high concentrations of CO2 (1000 ppm) treatment on 14:10 hour light: dark periods. However, there was no significant difference between the two CO2 concentrations where they were illuminated by 24 hours light in growth rate. The increasing CO2 concentration and light-dark periods were species-specific responses to photosynthesis and calcification rate for three selected calcifying microalgae.

Spatial distribution of seawater carbonate chemistry and hydrodynamic controls in a low-inflow estuary

Coastal and estuarine systems play an important role in the global carbon cycle and often have complex carbonate chemistry dynamics due to a multitude of biogeochemical and physical drivers. Compared to classic estuaries, mechanisms driving the distribution of carbonate parameters in low-inflow estuaries are understudied. The spatial distribution of carbonate chemistry and hydrodynamic parameters were characterized in Morro Bay, a short and seasonally hypersaline estuary on the Central California Coast, during the dry, low-inflow season to better understand in situ modifications. Sampling transects were completed in the main channel in June, August, and September of 2018, bracketing both a high and low tide on each date. Temperature, salinity, total alkalinity, and dissolved inorganic carbon all increased from the mouth to the back of the estuary, with larger values observed during the low tide. pH values decreased towards the back of the bay, and had little variation between high and low tide for June and August transects. Flushing times (estimated using a salt-budget model approach) also increased toward the back of the bay which led to hypersaline conditions. Salinity alone only explained 20–33% of observed changes in total alkalinity and 13–22% of observed changes in dissolved inorganic carbon throughout the bay. The remaining changes in total alkalinity and dissolved inorganic carbon were likely driven by biogeochemical modifications enhanced by extended flushing times, particularly in the back bay. Prior to this project, Morro Bay experienced a recent, rapid collapse of eelgrass, the major biogenic habitat. In the last four years eelgrass in Morro Bay appears to be on a recovery trajectory; therefore, this study provides a baseline whereby future studies can evaluate carbonate chemistry changes associated with potential eelgrass recovery and expansion. This study highlights the unique hydrodynamic exchange in seasonally low-inflow estuaries and its potentially large role in influencing local carbonate chemistry and ocean acidification.