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  • photosynthesis  (2)
  • Acid-base regulation; Alkalinity, total; Animalia; Aragonite saturation state; Balanophyllia europaea; Benthic animals; Benthos; Bicarbonate ion; Boron/Calcium ratio; Boron/Calcium ratio, standard error; Calcification/Dissolution; Calcification rate of calcium carbonate; Calcifying fluid, aragonite saturation state; Calcifying fluid, carbonate ion; Calcifying fluid, carbonate ion, standard error; Calcifying fluid, dissolved inorganic carbon; Calcifying fluid, dissolved inorganic carbon, standard error; Calcifying fluid, pH; Calcifying fluid, pH, standard error; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Cnidaria; CO2 vent; Coast and continental shelf; Field observation; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Gross calcification rate, relative; Gross calcification rate of calcium carbonate; Mediterranean Sea; Net calcification rate, relative; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH change; pH change, standard error; Ratio; Ratio, standard error; Registration number of species; Salinity; Single species; Site; Species; Temperate; Temperature, water; Type; Uniform resource locator/link to reference; δ11B; δ11B, standard deviation  (1)
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  • 1
    ISSN: 1573-5176
    Keywords: algal growth ; Porphyra ; inorganic carbon (Ci) ; photosynthesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Photosynthetic (oxygen evolution) and growth (biomass increase) responses to ambient pH and inorganic carbon (Ci) supply were determined for Porphyralinearis grown in 0.5 L glass cylinders in the laboratory, or in 40 L fibreglass outdoor tanks with running seawater. While net photosynthetic rates were uniform at pH 6.0–8.0, dropping only at pH 8.7, growth rates were significantly affected by pH levels other than that of seawater (c. pH 8.3). In glass cylinders, weekly growth rates averaged 76% at external pH 8.0, 13% at pH 8.7 and 26% at pH 7.0. Photosynthetic O2 evolution on a daily basis(i.e. total O2 evolved during day time less total O2 consumed during night time) was similar to the growth responses at all experimental pH levels, apparently due to high dark respiration rates measured at acidic pH. Weekly growth rates averaged 53% in algae grown in fibreglass tanks aerated with regular air (360 mg L-1 CO2) and 28% in algae grown in tanks aerated with CO2-enriched air (750 mg L-1 CO2). The pH of the seawater medium in which P. linear is was grown increased slightly during the day and only rarely reached 9.0. The pH at the boundary layer of algae submerged in seawater increased in response to light reaching, about pH 8.9 within minutes, or remained unchanged for algae submerged in a CO2-free artificial sea water medium. Photosynthesis of P. linearissaturated at Ci concentrations of seawater (K0.5560 μM at pH 8.2) and showed low photosynthetic affinity for CO2(K0.5 61 μM) at pH 6.0. It is therefore concluded that P. linearisuses primarily CO2 with HCO3 - being an alternative source of Ci for photosynthesis. Its fast growth could be related to the enzyme carbonic anhydrase whose activity was detected intra- and extracellularly.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-5176
    Keywords: desiccation ; growth ; growth model ; inorganic carbon ; nutrients ; photoperiod ; photosynthesis ; pigments ; Porphyra linearis ; PPF ; respiration ; temperature ; water velocity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The effect of environmental parameters on the growthof Porphyra linearis gametophytes was examinedunder controlled conditions, and related to themultilinear regression growth model recently developedfor this seaweed under coastal conditions in theeastern Mediterranean. Growth chambers, a gradienttable, special culture devices and analytical methodswere combined for this culture study.The major factors significantly controlling thegrowth rate of the P. linearis gametophytein glass dishes were: photoperiod, temperature, agein culture, photosynthetic photon flux (PPF), salinityand water dynamics. Maximal growth occurred underdaylength of 12 h, medium temperature (15–20 °C), low PPF (70–140 μmol photon m-2s-1), ambient salinity (30–40 ppt), 1–3 h ofdaily air exposure, and water velocity of 4 cm s-1.Photosynthesis and respiration rates weredominantly affected by daylength and temperature,while the concentration of pigments was dominantlyaffected by PPF and temperature.These conditions correspond well to the optimalnatural growth environment of this local species andare in agreement with the optimum estimated throughthe recently developed outdoor mathematical growthmodel.
    Type of Medium: Electronic Resource
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  • 3
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    PANGAEA
    In:  Supplement to: Wall, Marlene; Prada, Fiorella; Fietzke, Jan; Caroselli, Erik; Dubinsky, Zvy; Brizi, Leonardo; Fantazzini, Paola; Franzellitti, Silvia; Montagna, Paolo; Falini, Giuseppe; Goffredo, Stefano (2019): Linking Internal Carbonate Chemistry Regulation and Calcification in Corals Growing at a Mediterranean CO2 Vent. Frontiers in Marine Science, 6, https://doi.org/10.3389/fmars.2019.00699
    Publication Date: 2024-03-15
    Description: Corals exert a strong biological control over their calcification processes, but there is a lack of knowledge on their capability of long-term acclimatization to ocean acidification (OA). We used a dual geochemical proxy approach to estimate the calcifying fluid pH (pHcf) and carbonate chemistry of a Mediterranean coral (Balanophyllia europaea) naturally growing along a pH gradient (range: pHTS 8.07–7.74). The pHcf derived from skeletal boron isotopic composition (δ11B) was 0.3–0.6 units above seawater values and homogeneous along the gradient (mean +/- SEM: Site 1 = 8.39 +/- 0.03, Site 2 = 8.34 +/- 0.03, Site 3 = 8.34 +/- 0.02). Also carbonate ion concentration derived from B/Ca was homogeneous [mean +/- SEM (μmol /kg): Site 1 = 579 +/- 34, Site 2 = 541 +/- 27, Site 3 = 568 +/- 30] regardless of seawater pH. Furthermore, gross calcification rate (GCR, mass of CaCO3 deposited on the skeletal unit area per unit of time), estimated by a “bio-inorganic model” (IpHRAC), was homogeneous with decreasing pH. The homogeneous GCR, internal pH and carbonate chemistry confirm that the features of the “building blocks” – the fundamental structural components – produced by the biomineralization process were substantially unaffected by increased acidification. Furthermore, the pH up-regulation observed in this study could potentially explain the previous hypothesis that less “building blocks” are produced with increasing acidification ultimately leading to increased skeletal porosity and to reduced net calcification rate computed by including the total volume of the pore space. In fact, assuming that the available energy at the three sites is the same, this energy at the low pH sites could be partitioned among fewer calicoblastic cells that consume more energy given the larger difference between external and internal pH compared to the control, leading to the production of less building blocks (i.e., formation of pores inside the skeleton structure, determining increased porosity). However, we cannot exclude that also dissolution may play a role in increasing porosity. Thus, the ability of scleractinian corals to maintain elevated pHcf relative to ambient seawater might not always be sufficient to counteract declines in net calcification under OA scenarios.
    Keywords: Acid-base regulation; Alkalinity, total; Animalia; Aragonite saturation state; Balanophyllia europaea; Benthic animals; Benthos; Bicarbonate ion; Boron/Calcium ratio; Boron/Calcium ratio, standard error; Calcification/Dissolution; Calcification rate of calcium carbonate; Calcifying fluid, aragonite saturation state; Calcifying fluid, carbonate ion; Calcifying fluid, carbonate ion, standard error; Calcifying fluid, dissolved inorganic carbon; Calcifying fluid, dissolved inorganic carbon, standard error; Calcifying fluid, pH; Calcifying fluid, pH, standard error; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Cnidaria; CO2 vent; Coast and continental shelf; Field observation; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Gross calcification rate, relative; Gross calcification rate of calcium carbonate; Mediterranean Sea; Net calcification rate, relative; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH change; pH change, standard error; Ratio; Ratio, standard error; Registration number of species; Salinity; Single species; Site; Species; Temperate; Temperature, water; Type; Uniform resource locator/link to reference; δ11B; δ11B, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 1459 data points
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