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  • 2010-2014  (14)
  • 2010  (14)
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  • 2010-2014  (14)
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  • 1
    Publication Date: 2023-03-09
    Description: Zooxanthellate colonies of the scleractinian coral Astrangia poculata were grown under combinations of ambient and elevated nutrients (5 µM NO, 0.3 µM PO4, and 2nM Fe) and CO2 (780 ppmv) treatments for a period of 6 months. Coral calcification rates, estimated from buoyant weights, were not significantly affected by moderately elevated nutrients at ambient CO2 and were negatively affected by elevated CO2 at ambient nutrient levels. However, calcification by corals reared under elevated nutrients combined with elevated CO2 was not significantly different from that of corals reared under ambient conditions, suggesting that CO2 enrichment can lead to nutrient limitation in zooxanthellate corals. A conceptual model is proposed to explain how nutrients and CO2 interact to control zooxanthellate coral calcification. Nutrient limited corals are unable to utilize an increase in dissolved inorganic carbon (DIC) as nutrients are already limiting growth, thus the effect of elevated CO2 on saturation state drives the calcification response. Under nutrient replete conditions, corals may have the ability to utilize more DIC, thus the calcification response to CO2 becomes the product of a negative effect on saturation state and a positive effect on gross carbon fixation, depending upon which dominates, the calcification response can be either positive or negative. This may help explain how the range of coral responses found in different studies of ocean acidification can be obtained.
    Keywords: Animalia; Astrangia poculata; Benthic animals; Benthos; Bottles or small containers/Aquaria (〈20 L); Calcification/Dissolution; Cnidaria; Coast and continental shelf; CTD/Rosette; CTD-RO; EPOCA; EUR-OCEANS; European network of excellence for Ocean Ecosystems Analysis; European Project on Ocean Acidification; Great_Harbor_051104/14; Great_Harbor_051104/22; Great_Harbor_051105/06; Great_Harbor_051105/11; Great_Harbor_051105/15; Great_Harbor_060101/10; Great_Harbor_060101/18; Great_Harbor_061104/14; Great_Harbor_070119/16; Great_Harbor_070219/17; Great_Harbor_070319/16; Great_Harbor_070419/16; Great_Harbor_070519/18; Great_Harbor_070702/17; Great_Harbor_070720/17; Great_Harbor_070820/17; Great_Harbor_070920/18; Great_Harbor_080327/17; Great_Harbor_080423/17; Great_Harbor_080529/16; Great_Harbor_080623/17; Great_Harbor_080729/17; Great_Harbor_080831/18; Great_Harbor_081005/18; Great_Harbor_081109/18; Great_Harbor_081212/19; Great_Harbor_090219/20; Great_Harbor_090328/18; Great_Harbor_090430/18; Laboratory experiment; Macro-nutrients; North Atlantic; OA-ICC; Ocean Acidification International Coordination Centre; Single species; Temperate
    Type: Dataset
    Format: application/zip, 2 datasets
    Location Call Number Limitation Availability
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  • 2
    Publication Date: 2023-02-24
    Keywords: Alkalinity, total; Animalia; Astrangia poculata; Benthic animals; Benthos; Bottles or small containers/Aquaria (〈20 L); Carbon, inorganic, dissolved; Closed cell titration eg Brewer et al 1986; Cnidaria; Coast and continental shelf; CTD/Rosette; CTD-RO; EPOCA; EUR-OCEANS; European network of excellence for Ocean Ecosystems Analysis; European Project on Ocean Acidification; Event label; Great_Harbor_051104/14; Great_Harbor_051104/22; Great_Harbor_051105/06; Great_Harbor_051105/11; Great_Harbor_051105/15; Great_Harbor_060101/10; Great_Harbor_060101/18; Great_Harbor_061104/14; Great_Harbor_070119/16; Great_Harbor_070219/17; Great_Harbor_070319/16; Great_Harbor_070419/16; Great_Harbor_070519/18; Great_Harbor_070702/17; Great_Harbor_070720/17; Great_Harbor_070820/17; Great_Harbor_070920/18; Great_Harbor_080327/17; Great_Harbor_080423/17; Great_Harbor_080529/16; Great_Harbor_080623/17; Great_Harbor_080729/17; Great_Harbor_080831/18; Great_Harbor_081005/18; Great_Harbor_081109/18; Great_Harbor_081212/19; Great_Harbor_090219/20; Great_Harbor_090328/18; Great_Harbor_090430/18; Guildline autosal salinometer; Laboratory experiment; Macro-nutrients; Onset logger; Salinity; Single species; Temperate; Temperature, water
    Type: Dataset
    Format: text/tab-separated-values, 228 data points
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  • 3
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    PANGAEA
    In:  Supplement to: Ries, Justin B; Cohen, Anne L; McCorkle, Daniel C (2010): A nonlinear calcification response to CO2-induced ocean acidification by the coral Oculina arbuscula. Coral Reefs, 29(3), 661-674, https://doi.org/10.1007/s00338-010-0632-3
    Publication Date: 2024-03-15
    Description: Anthropogenic elevation of atmospheric pCO2 is predicted to cause the pH of surface seawater to decline by 0.3-0.4 units by 2100 AD, causing a 50% reduction in seawater [CO3] and undersaturation with respect to aragonite in high-latitude surface waters. We investigated the impact of CO2-induced ocean acidification on the temperate scleractinian coral Oculina arbuscula by rearing colonies for 60 days in experimental seawaters bubbled with air-CO2 gas mixtures of 409, 606, 903, and 2,856 ppm pCO2, yielding average aragonite saturation states (Omega aragonite) of 2.6, 2.3, 1.6, and 0.8. Measurement of calcification (via buoyant weighing) and linear extension (relative to a 137Ba/138Ba spike) revealed that skeletal accretion was only minimally impaired by reductions in Omega aragonite from 2.6 to 1.6, although major reductions were observed at 0.8 (undersaturation). Notably, the corals continued accreting new skeletal material even in undersaturated conditions, although at reduced rates. Correlation between rates of linear extension and calcification suggests that reduced calcification under Omega aragonite = 0.8 resulted from reduced aragonite accretion, rather than from localized dissolution. Accretion of pure aragonite under each Omega aragonite discounts the possibility that these corals will begin producing calcite, a less soluble form of CaCO3, as the oceans acidify. The corals' nonlinear response to reduced Omega aragonite and their ability to accrete new skeletal material in undersaturated conditions suggest that they strongly control the biomineralization process. However, our data suggest that a threshold seawater [CO3] exists, below which calcification within this species (and possibly others) becomes impaired. Indeed, the strong negative response of O. arbuscula to Omega aragonite= 0.8 indicates that their response to future pCO2-induced ocean acidification could be both abrupt and severe once the critical Omega aragoniteis reached.
    Keywords: Alkalinity, Gran titration (Gran, 1950); Alkalinity, total; Alkalinity, total, standard deviation; Animalia; Aragonite saturation state; Aragonite saturation state, standard deviation; Benthic animals; Benthos; Bicarbonate; Bicarbonate ion; Bicarbonate ion, standard deviation; Buoyant mass; Buoyant weighing technique according to Davies (1989); Calcification/Dissolution; Calcification rate; Calcite saturation state; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbonate ion; Carbonate ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, standard deviation; Carbon dioxide, total; Cnidaria; Coast and continental shelf; Containers and aquaria (20-1000 L or 〈 1 m**2); EPOCA; EUR-OCEANS; European network of excellence for Ocean Ecosystems Analysis; European Project on Ocean Acidification; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Guildline autosal salinometer; Infrared pCO2 analyzer (Qubit S151); Laboratory experiment; Linear extension; Measured; North Atlantic; OA-ICC; Ocean Acidification International Coordination Centre; Oculina arbuscula; Partial-immersion mercury-glass thermometer; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, standard deviation; pH meter (Orion); Salinity; Salinity, standard deviation; Sample ID; Single species; Species; Temperate; Temperature, standard deviation; Temperature, water
    Type: Dataset
    Format: text/tab-separated-values, 1941 data points
    Location Call Number Limitation Availability
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  • 4
    Publication Date: 2024-05-22
    Description: Zooxanthellate colonies of the scleractinian coral Astrangia poculata were grown under combinations of ambient and elevated nutrients (5 µM NO, 0.3 µM PO4, and 2nM Fe) and CO2 (780 ppmv) treatments for a period of 6 months. Coral calcification rates, estimated from buoyant weights, were not significantly affected by moderately elevated nutrients at ambient CO2 and were negatively affected by elevated CO2 at ambient nutrient levels. However, calcification by corals reared under elevated nutrients combined with elevated CO2 was not significantly different from that of corals reared under ambient conditions, suggesting that CO2 enrichment can lead to nutrient limitation in zooxanthellate corals. A conceptual model is proposed to explain how nutrients and CO2 interact to control zooxanthellate coral calcification. Nutrient limited corals are unable to utilize an increase in dissolved inorganic carbon (DIC) as nutrients are already limiting growth, thus the effect of elevated CO2 on saturation state drives the calcification response. Under nutrient replete conditions, corals may have the ability to utilize more DIC, thus the calcification response to CO2 becomes the product of a negative effect on saturation state and a positive effect on gross carbon fixation, depending upon which dominates, the calcification response can be either positive or negative. This may help explain how the range of coral responses found in different studies of ocean acidification can be obtained.
    Keywords: Alkalinity, Gran titration (Gran, 1950); Alkalinity, total; Alkalinity, total, standard deviation; Animalia; Aragonite saturation state; Astrangia poculata; Benthic animals; Benthos; Bicarbonate ion; Bottles or small containers/Aquaria (〈20 L); Buoyant weighing technique according to Davies (1989); Calcification/Dissolution; Calcification rate; Calcification rate, standard deviation; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, partial pressure, standard deviation; Cnidaria; Coast and continental shelf; Continuous flow injection system, FIAlab 2600; EPOCA; EUR-OCEANS; European network of excellence for Ocean Ecosystems Analysis; European Project on Ocean Acidification; Experimental treatment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Hach conductivity probe; Infrared pCO2 analyzer (Qubit S151); Laboratory experiment; Macro-nutrients; Nitrate and Nitrite; Nitrate and Nitrite, standard deviation; Onset logger; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; Phosphate; Phosphate, standard deviation; Salinity; Salinity, standard deviation; Silicate; Silicon, standard deviation; Single species; Temperate; Temperature, standard deviation; Temperature, water
    Type: Dataset
    Format: text/tab-separated-values, 104 data points
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  • 5
    Publication Date: 2022-05-25
    Description: Author Posting. © Oceanography Society, 2009. This article is posted here by permission of Oceanography Society for personal use, not for redistribution. The definitive version was published in Oceanography 22 no. 4 (2009): 118-127.
    Description: Stony corals build hard skeletons of calcium carbonate (CaCO3) by combining calcium with carbonate ions derived, ultimately, from seawater. The concentration of carbonate ions relative to other carbonate species in seawater is rather low, so corals expend energy to raise the pH of seawater sequestered in an isolated, extracellular compartment where crystal growth occurs. This action converts plentiful bicarbonate ions to the carbonate ions required for calcification, allowing corals to produce CaCO3 about 100 times faster than it could otherwise form. It is this rapid and efficient production of CaCO3 crystals that enables corals to build coral reefs. Ocean acidification reduces the pH and thus the abundance of carbonate ions in seawater. Corals living in acidified seawater continue to produce CaCO3 and expend as much energy as their counterparts in normal seawater to raise the pH of the calcifying fluid. However, in acidified seawater, corals are unable to elevate the concentration of carbonate ions to the level required for normal skeletal growth. In several experiments, we found that boosting the energetic status of corals by enhanced heterotrophic feeding or moderate increases in inorganic nutrients helped to offset the negative impact of ocean acidification. However, this built-in defense is unlikely to benefit corals as levels of CO2 in the atmosphere continue to rise. Most climate models predict that the availability of inorganic nutrients and plankton in the surface waters where corals live will decrease as a consequence of global warming. Thus, corals and coral reefs may be significantly more vulnerable to ocean acidification than previously thought.
    Description: Anne L. Cohen acknowledges support from the WHOI Directorate for our Marine Calcification and Culture Labs, from WHOI’s Ocean Life and Tropical Research Institutes, and from NSF CO-0648157. Michael Holcomb’s graduate research was supported in part by an NSF graduate student fellowship, an MIT Presidential Award, and an International Coral Reef Society fellowship.
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: application/pdf
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  • 6
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    Unknown
    American Geophysical Union
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2004. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 31 (2004): L16310, doi:10.1029/2004GL020600.
    Description: The strontium-to-calcium ratio (Sr/Ca) of reef coral skeleton is an important tool for reconstructing past sea surface temperatures (SSTs). However, the accuracy of paleoSSTs derived from fossil coral Sr/Ca is challenged by evidence that physiological processes influence skeletal chemistry. Here we show that water level variations from tidal forcing are correlated with changes in coral Sr/Ca that cannot be accounted for by changes in SST. Ion microprobe measurements of Sr/Ca ratios in a Pacific Porites lutea reveal high-frequency variations at periods of ~6, ~10, and ~25 days. The relationship between Sr/Ca and temperature on these short timescales does not follow trends observed at longer periods, indicating that an additional forcing is required to explain our observations. We demonstrate that Sr/Ca is correlated with both tidal water level variations and SST, and that their contributions to the Sr/Ca content of the skeleton vary as a function of period. We propose that water level influences Sr/Ca indirectly via modulation of photosynthetically-active radiation (PAR) that drives large changes in zooxanthellate photosynthesis.
    Description: This research was supported by WHOI Ocean Life Institute grant 25051316 to ALC; NSF grants EAR-9628749 and EAR-9904400 to the WHOI Northeast National Ion Microprobe Facility; DAMD 17-93-J-3052 supported ALC’s fieldwork on JA.
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: application/pdf
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  • 7
    Publication Date: 2022-05-25
    Description: Author Posting. © The Author(s), 2010. This is the author's version of the work. It is posted here by permission of Elsevier B.V. for personal use, not for redistribution. The definitive version was published in Journal of Experimental Marine Biology and Ecology 386 (2010): 27-33, doi:10.1016/j.jembe.2010.02.007.
    Description: Zooxanthellate colonies of the scleractinian coral Astrangia poculata were grown under combinations of ambient and elevated nutrients (5 μM NO3 -, 0.3 μM PO4 -3, and 2 nM Fe+2) and CO2 (~780 ppmv) treatments for a period of 6 months. Coral calcification rates, estimated from buoyant weights, were not significantly affected by moderately elevated nutrients at ambient CO2 and were negatively affected by elevated CO2 at ambient nutrient levels. However, calcification by corals reared under elevated nutrients combined with elevated CO2 was not significantly different from that of corals reared under ambient conditions, suggesting that CO2 enrichment can lead to nutrient limitation in zooxanthellate corals. A conceptual model is proposed to explain how nutrients and CO2 interact to control zooxanthellate coral calcification. Nutrient limited corals are unable to utilize an increase in dissolved inorganic carbon (DIC) as nutrients are already limiting growth, thus the effect of elevated CO2 on saturation state drives the calcification response. Under nutrient replete conditions, corals may have the ability to utilize more DIC, thus the calcification response to CO2 becomes the product of a negative effect on saturation state and a positive effect on gross carbon fixation, depending upon which dominates, the calcification response can be either positive or negative. This may help explain how the range of coral responses found in different studies of ocean acidification can be obtained.
    Description: Funding for this work was provided by the Ocean Life Institute, NSF OCE-0648157, and an International Society for Reef Studies / Ocean Conservancy Fellowship. This material is based upon work supported under a National Science Foundation Graduate Research Fellowship.
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
    Format: application/pdf
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  • 8
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2009. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geochemistry Geophysics Geosystems 19 (2009): Q07005, doi:10.1029/2009GC002411.
    Description: We reared primary polyps (new recruits) of the common Atlantic golf ball coral Favia fragum for 8 days at 25°C in seawater with aragonite saturation states ranging from ambient (Ω = 3.71) to strongly undersaturated (Ω = 0.22). Aragonite was accreted by all corals, even those reared in strongly undersaturated seawater. However, significant delays, in both the initiation of calcification and subsequent growth of the primary corallite, occurred in corals reared in treatment tanks relative to those grown at ambient conditions. In addition, we observed progressive changes in the size, shape, orientation, and composition of the aragonite crystals used to build the skeleton. With increasing acidification, densely packed bundles of fine aragonite needles gave way to a disordered aggregate of highly faceted rhombs. The Sr/Ca ratios of the crystals, measured by SIMS ion microprobe, increased by 13%, and Mg/Ca ratios decreased by 45%. By comparing these variations in elemental ratios with results from Rayleigh fractionation calculations, we show that the observed changes in crystal morphology and composition are consistent with a 〉80% decrease in the amount of aragonite precipitated by the corals from each “batch” of calcifying fluid. This suggests that the saturation state of fluid within the isolated calcifying compartment, while maintained by the coral at levels well above that of the external seawater, decreased systematically and significantly as the saturation state of the external seawater decreased. The inability of the corals in acidified treatments to achieve the levels of calcifying fluid supersaturation that drive rapid crystal growth could reflect a limit in the amount of energy available for the proton pumping required for calcification. If so, then the future impact of ocean acidification on tropical coral ecosystems may depend on the ability of individuals or species to overcome this limitation and achieve the levels of calcifying fluid supersaturation required to ensure rapid growth.
    Description: This study was supported by NSF OCE-0648157 and NSF OCE-0823527 and the Bermuda Institute for Ocean Sciences.
    Keywords: Ocean acidification ; Coral ; Sr/Ca ; Calcification ; Mg/Ca ; Biomineralization
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: application/pdf
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  • 9
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2009. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 36 (2009): L11703, doi:10.1029/2009GL038677.
    Description: Proxy reconstructions and model simulations suggest that steeper interhemispheric sea surface temperature (SST) gradients lead to southerly Intertropical Convergence Zone (ITCZ) migrations during periods of North Atlantic cooling, the most recent of which was the Little Ice Age (LIA; ∼100–450 yBP). Evidence suggesting low-latitude Atlantic cooling during the LIA was relatively small (〈1°C) raises the possibility that the ITCZ may have responded to a hemispheric SST gradient originating in the extratropics. We use an atmospheric general circulation model (AGCM) to investigate the relative influence of low-latitude and extratropical SSTs on the meridional position of the ITCZ. Our results suggest that the ITCZ responds primarily to local, low-latitude SST anomalies and that small cool anomalies (〈0.5°C) can reproduce the LIA precipitation pattern suggested by paleoclimate proxies. Conversely, even large extratropical cooling does not significantly impact low-latitude hydrology in the absence of ocean-atmosphere interaction.
    Description: This work was supported by NSF grants OCE 0623364 and ATM 033746 as well as the student research fund of MIT’s Department of Earth, Atmospheric and Planetary Science.
    Keywords: Climate ; ITCZ ; Little Ice Age
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: application/pdf
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  • 10
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2005. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Paleoceanography 20 (2005): PA4016, doi:10.1029/2005PA001140.
    Description: Strontium to calcium ratios (Sr/Ca) are reported for a massive brain coral Diploria labyrinthiformis collected from the south shore of Bermuda and are strongly correlated with both sea surface temperature (SST) and mean annual skeletal growth rate. High Sr/Ca ratios correspond with cold SSTs and slow skeletal growth rate and vice versa. We provide a quantitative calibration of Sr/Ca to extension rate and SST along the axis of maximum growth and derive a growth-dependent Sr/Ca–SST calibration equation to reconstruct western subtropical North Atlantic SSTs for the past 223 years. When the influence of growth rate is excluded from the calibration, Sr/Ca ratios yield SSTs that are too cold during cool anomalies and too warm during warm anomalies. Toward the end of the Little Ice Age (∼1850), SST changes derived using a calibration that is not growth-dependent are exaggerated by a factor of 2 relative to those from the growth-corrected model that yields SSTs ∼1.5°C cooler than today. Our results indicate that incorporation of growth rate effects into coral Sr/Ca calibrations may improve the accuracy of SSTs derived from living and fossil corals.
    Description: A Stanley Watson Foundation Fellowship (N.F.G.), and grants from NSF (OCE-0402728) and WHOI (K.A.H., A.L.C., and M.S.M.) supported this work.
    Keywords: SST ; Coral Sr/Ca ; Growth rate
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: application/pdf
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