Xinping Hu

Decrease in the CO2 Uptake Capacity in an Ice-Free Arctic Ocean Basin

Sinking in Slowly As the Arctic warms and its sea ice continues to melt, more of the ocean surface will be exposed, creating the potential for greater uptake of carbon dioxide from the atmosphere. Cai et al. (p. 556, published online 22 July) present results from a series of Arctic Ocean transects that show that the amount of CO2 in the surface waters has increased greatly recently. This will act as a barrier to future CO2 uptake and suggests that the Arctic Ocean will not become the large CO2 sink that some have predicted. The current carbon dioxide levels in the Arctic Ocean basin will limit further uptake under ice-free conditions. It has been predicted that the Arctic Ocean will sequester much greater amounts of carbon dioxide (CO2) from the atmosphere as a result of sea ice melt and increasing primary productivity. However, this prediction was made on the basis of observations from either highly productive ocean margins or ice-covered basins before the recent major ice retreat. We report here a high-resolution survey of sea-surface CO2 concentration across the Canada Basin, showing a great increase relative to earlier observations. Rapid CO2 invasion from the atmosphere and low biological CO2 drawdown are the main causes for the higher CO2, which also acts as a barrier to further CO2 invasion. Contrary to the current view, we predict that the Arctic Ocean basin will not become a large atmospheric CO2 sink under ice-free conditions.

Coral Energy Reserves and Calcification in a High-CO2 World at Two Temperatures

Rising atmospheric CO2 concentrations threaten coral reefs globally by causing ocean acidification (OA) and warming. Yet, the combined effects of elevated pCO2 and temperature on coral physiology and resilience remain poorly understood. While coral calcification and energy reserves are important health indicators, no studies to date have measured energy reserve pools (i.e., lipid, protein, and carbohydrate) together with calcification under OA conditions under different temperature scenarios. Four coral species, Acropora millepora, Montipora monasteriata, Pocillopora damicornis, Turbinaria reniformis, were reared under a total of six conditions for 3.5 weeks, representing three pCO2 levels (382, 607, 741 µatm), and two temperature regimes (26.5, 29.0°C) within each pCO2 level. After one month under experimental conditions, only A. millepora decreased calcification (−53%) in response to seawater pCO2 expected by the end of this century, whereas the other three species maintained calcification rates even when both pCO2 and temperature were elevated. Coral energy reserves showed mixed responses to elevated pCO2 and temperature, and were either unaffected or displayed nonlinear responses with both the lowest and highest concentrations often observed at the mid-pCO2 level of 607 µatm. Biweekly feeding may have helped corals maintain calcification rates and energy reserves under these conditions. Temperature often modulated the response of many aspects of coral physiology to OA, and both mitigated and worsened pCO2 effects. This demonstrates for the first time that coral energy reserves are generally not metabolized to sustain calcification under OA, which has important implications for coral health and bleaching resilience in a high-CO2 world. Overall, these findings suggest that some corals could be more resistant to simultaneously warming and acidifying oceans than previously expected.

Microelectrode characterization of coral daytime interior pH and carbonate chemistry

Reliably predicting how coral calcification may respond to ocean acidification and warming depends on our understanding of coral calcification mechanisms. However, the concentration and speciation of dissolved inorganic carbon (DIC) inside corals remain unclear, as only pH has been measured while a necessary second parameter to constrain carbonate chemistry has been missing. Here we report the first carbonate ion concentration ([CO32−]) measurements together with pH inside corals during the light period. We observe sharp increases in [CO32−] and pH from the gastric cavity to the calcifying fluid, confirming the existence of a proton (H+) pumping mechanism. We also show that corals can achieve a high aragonite saturation state (Ωarag) in the calcifying fluid by elevating pH while at the same time keeping [DIC] low. Such a mechanism may require less H+-pumping and energy for upregulating pH compared with the high [DIC] scenario and thus may allow corals to be more resistant to climate change related stressors.

THE WIDESPREAD OCCURRENCE OF COUPLED CARBONATE DISSOLUTION/REPRECIPITATION IN SURFACE SEDIMENTS ON THE BAHAMAS BANK

Using two complimentary approaches (pore water advection/diffusion/ reaction modeling and stable isotope mass balance calculations) we show that carbonate dissolution/reprecipitation occurs on early diagenetic time scales across a broad range of sediments on the Great Bahamas Bank. The input of oxygen into the sediments, which strongly controls sediment carbonate dissolution, has two major sources—belowground input by seagrasses (that is, seagrass O2 pumping), and permeability-driven advective pore water exchange. The relative importance of these O2 delivery mechanisms depends on both seagrass density, and on how bottom water flow interacts with the seagrass canopy and leads to this advective exchange. Dissolution appears to involve the preferential dissolution of high-Mg calcite, and the rates of dissolution increase linearly with increasing seagrass density. Isotopic evidence of dissolution/reprecipitation is consistent with the occurrence of Ostwald ripening as the mechanism of reprecipitation, in which smaller crystals dissolve and then reprecipitate as larger crystals, with little or no change in mineralogy. Estimates of the aerially-integrated dissolution flux on the Bahamas Bank suggest that carbonate dissolution is an important loss term in the budget of shallow water carbonate sediments, and that on-bank carbonate dissolution, rather than offshore transport, may represent an important sink for gross shallow water carbonate production. Dissolution in carbonate bank and bay sediments may also be a significant alkalinity source to the surface ocean, and should be considered in global alkalinity/carbonate budget. Finally, coupled dissolution/reprecipitation may have a major impact on the stable isotope composition of carbonate sediments that are ultimately preserved in the rock record. These processes may therefore need to be considered, for example, when using carbon isotope records to obtain information on the operation of the global carbon cycle during the Phanerozoic.

Physiological response to elevated temperature and pCO2 varies across four Pacific coral species: Understanding the unique host + symbiont response

The physiological response to individual and combined stressors of elevated temperature and pCO2 were measured over a 24-day period in four Pacific corals and their respective symbionts (Acropora millepora/Symbiodinium C21a, Pocillopora damicornis/Symbiodinium C1c-d-t, Montipora monasteriata/Symbiodinium C15, and Turbinaria reniformis/Symbiodinium trenchii). Multivariate analyses indicated that elevated temperature played a greater role in altering physiological response, with the greatest degree of change occurring within M. monasteriata and T. reniformis. Algal cellular volume, protein, and lipid content all increased for M. monasteriata. Likewise, S. trenchii volume and protein content in T. reniformis also increased with temperature. Despite decreases in maximal photochemical efficiency, few changes in biochemical composition (i.e. lipids, proteins, and carbohydrates) or cellular volume occurred at high temperature in the two thermally sensitive symbionts C21a and C1c-d-t. Intracellular carbonic anhydrase transcript abundance increased with temperature in A. millepora but not in P. damicornis, possibly reflecting differences in host mitigated carbon supply during thermal stress. Importantly, our results show that the host and symbiont response to climate change differs considerably across species and that greater physiological plasticity in response to elevated temperature may be an important strategy distinguishing thermally tolerant vs. thermally sensitive species.

Long-Term Alkalinity Decrease and Acidification of Estuaries in Northwestern Gulf of Mexico

More than four decades of alkalinity and pH data (late 1960s to 2010) from coastal bays along the northwestern Gulf of Mexico were analyzed for temporal changes across a climatic gradient of decreasing rainfall and freshwater inflow, from northeast to southwest. The majority (16 out of 27) of these bays (including coastal waters) showed a long-term reduction in alkalinity at a rate of 3.0-21.6 μM yr(-1). Twenty-two bays exhibited pH decreases at a rate of 0.0014-0.0180 yr(-1). In contrast, a northernmost coastal bay exhibited increases in both alkalinity and pH. Overall, the two rates showed a significant positive correlation, indicating that most of these bays, especially those at lower latitudes, have been experiencing long-term acidification. The observed alkalinity decrease may be caused by reduced riverine alkalinity export, a result of precipitation decline under drought conditions, and freshwater diversion for human consumption, as well as calcification in these bays. A decrease in alkalinity inventory and accompanying acidification may have negative impacts on shellfish production in these waters. In addition, subsequent reduction in alkalinity export from these bays to the adjacent coastal ocean may also decrease the buffer capacity of the latter against future acidification.

Shallow Marine Carbonate Dissolution and Early Diagenesis-Implications from an Incubation Study

Surface carbonate sediments from sites on the Bahamas Bank with different seagrass densities were incubated across a range of O2 delivery rates, to study the controls on metabolic carbonate dissolution in these sediments. The results confirmed the 1:1 ratio between the rates of O2 consumption and carbonate dissolution, demonstrating that microbial respiration was the ratelimiting step in metabolic carbonate dissolution. Furthermore, the dissolution we observed was actually net dissolution resulting from coupled dissolution and reprecipitation. This carbonate reprecipitation occurs on the time scale of days, and significantly alters the pore water dissolved inorganic carbon (DIC) stable isotopic composition. The carbonate reprecipitation/dissolution ratios observed here were similar to those reported in the literature for other sediments. Dissolution/ reprecipitation appeared to involve preferential dissolution of high magnesium calcite and reprecipitation of a carbonate phase with a Mg content that was only slightly lower than that of the dissolving phase. This result agrees with conclusions in the literature that “Ostwald ripening” may be responsible for this reprecipitation.

Temporal variation and stoichiometric ratios of organic matter remineralization in bottom waters of the northern Gulf of Mexico during late spring and summer

An improved extended optimum multiparameter (eOMP) analysis was applied to hydrographic (temperature and salinity), and water chemistry data, including dissolved oxygen (O2), nutrients (nitrate plus nitrite, phosphate, and silicate), dissolved inorganic carbon (DIC), and total alkalinity (TAlk) data collected during late spring and summer from 2006 to 2012 in bottom waters off the Louisiana coast, to explore the dynamics and stoichiometry of DIC production during the development and maintenance of summer hypoxia. Our analysis demonstrated that DIC in bottom water was relatively low from April to June, but increased significantly in July, peaked in August, and dropped slightly in September. Furthermore, DIC production resulted from both aerobic organic carbon (OC) respiration and denitrification, as well as substantial loss due to vertical mixing with surface water. The average summer gross OC respiration rate was estimated to be 0.19 g C m−2 d−1, with the highest values occurring in late summer when hypoxic conditions dominated. We also found that Corg/N/P/-O2 remineralization ratios for aerobic respiration were generally consistent with the classic Redfield ratio (106/16/1/138) except individual C/N and C/P ratios were slightly lower, indicating that marine OC was the major source of the DIC production in the bottom water. This study quantified the role of temporal bottom-water microbial respiration to seasonal DIC dynamics and provided a means for studying the stoichiometry of biogeochemical processes in coastal waters.

Continental shelves as a variable but increasing global sink for atmospheric carbon dioxide

It has been speculated that the partial pressure of carbon dioxide (pCO2) in shelf waters may lag the rise in atmospheric CO2. Here, we show that this is the case across many shelf regions, implying a tendency for enhanced shelf uptake of atmospheric CO2. This result is based on analysis of long-term trends in the air–sea pCO2 gradient (ΔpCO2) using a global surface ocean pCO2 database spanning a period of up to 35 years. Using wintertime data only, we find that ΔpCO2 increased in 653 of the 825 0.5° cells for which a trend could be calculated, with 325 of these cells showing a significant increase in excess of +0.5 μatm yr−1 (p < 0.05). Although noisier, the deseasonalized annual data suggest similar results. If this were a global trend, it would support the idea that shelves might have switched from a source to a sink of CO2 during the last century.It remains unclear whether surface water partial pressure of CO2 (pCO2) in continental shelves tracks with increasing atmospheric pCO2. Here, the authors show that pCO2 in shelf waters lags behind rising atmospheric CO2 in a number of shelf regions, suggesting shelf uptake of atmospheric CO2.

Coral calcification under environmental change: a direct comparison of the alkalinity anomaly and buoyant weight techniques

Two primary methods—the buoyant weight (BW) and alkalinity anomaly (AA) techniques—are currently used to quantify net calcification rates (G) in scleractinian corals. However, it remains unclear whether they are directly comparable since the few method comparisons conducted to date have produced inconsistent results. Further, such a comparison has not been made for tropical corals. We directly compared GBW and GAA in four tropical and one temperate coral species cultured under various pCO2, temperature, and nutrient conditions. A range of protocols for conducting alkalinity depletion incubations was assessed. For the tropical corals, open-top incubations with manual stirring produced GAA that were highly correlated with and not significantly different from GBW. Similarly, GAA of the temperate coral was not significantly different from GBW when incubations provided water motion using a pump, but were significantly lower than GBW by 16% when water motion was primarily created by aeration. This shows that the two techniques can produce comparable calcification rates in corals but only when alkalinity depletion incubations are conducted under specific conditions. General recommendations for incubation protocols are made, especially regarding adequate water motion and incubation times. Further, the re-analysis of published data highlights the importance of using appropriate regression statistics when both variables are random and measured with error. Overall, we recommend the AA technique for investigations of community and short-term day versus night calcification, and the BW technique to measure organism calcification rates integrated over longer timescales due to practical limitations of both methods. Our findings will facilitate the direct comparison of studies measuring coral calcification using either method and thus have important implications for the fields of ocean acidification research and coral biology in general.