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  • Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Benthos; Bicarbonate ion; Bicarbonate ion, standard deviation; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Calculated using SWCO2 (Hunter, 2007); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbonate ion; Carbonate ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, partial pressure, standard deviation; Chromista; Closed cell titration; Coast and continental shelf; Dihydrogen carbonate; Dihydrogen carbonate, standard deviation; 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); Identification; Laboratory experiment; Macroalgae; Macrocystis pyrifera; Macrocystis pyrifera, gametophyte size; Macrocystis pyrifera, gametophyte size, standard deviation; Macrocystis pyrifera, germination rate; Macrocystis pyrifera, germination rate, standard deviation; Macrocystis pyrifera, sex ratio; Macrocystis pyrifera, sex ratio, standard deviation; OA-ICC; Ocean Acidification International Coordination Centre; Ochrophyta; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, standard deviation; pH meter (Orion 720A); Reproduction; Salinity; Single species; South Pacific; Temperate; Temperature, water  (1)
  • Alkalinity, total; Aragonite saturation state; Aromoana; Benthos; Bicarbonate ion; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Calculated using SWCO2 (Hunter, 2007); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Carbonic anhydrase activity; Carbonic anhydrase activity, standard error; Chromista; Coast and continental shelf; Coulometric titration; EXP; Experiment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Inhibition of net photosynthesis; Inhibition of net photosynthesis, standard error; Laboratory experiment; Macroalgae; Macrocystis pyrifera; Net photosynthesis rate, oxygen; Net photosynthesis rate, oxygen, standard error; OA-ICC; Ocean Acidification International Coordination Centre; Ochrophyta; Other metabolic rates; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; Potentiometric titration; Primary production/Photosynthesis; Salinity; Single species; South Pacific; Species; Spectrophotometric; Temperate; Temperature, water  (1)
  • 2010-2014  (2)
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  • 2010-2014  (2)
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  • 1
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    PANGAEA
    In:  Supplement to: Fernández, Pamela A; Hurd, Catriona L; Roleda, Michael Y (2014): Bicarbonate uptake via an anion exchange protein is the main mechanism of inorganic carbon acquisition by the giant kelp Macrocystis pyrifera (Laminariales, Phaeophyceae) under variable pH. Journal of Phycology, 50(6), 998-1008, https://doi.org/10.1111/jpy.12247
    Publication Date: 2024-03-15
    Description: Macrocystis pyrifera is a widely distributed, highly productive, seaweed. It is known to use bicarbonate (HCO3-) from seawater in photosynthesis and the main mechanism of utilization is attributed to the external catalyzed dehydration of HCO3- by the surface-bound enzyme carbonic anhydrase (CAext). Here, we examined other putative HCO3- uptake mechanisms in M. pyrifera under pHT 9.00 (HCO3-: CO2 = 940:1) and pHT 7.65 (HCO3-: CO2 = 51:1). Rates of photosynthesis, and internal CA (CAint) and CAext activity were measured following the application of AZ which inhibits CAext, and DIDS which inhibits a different HCO3- uptake system, via an anion exchange (AE) protein. We found that the main mechanism of HCO3- uptake by M. pyrifera is via an AE protein, regardless of the HCO3-: CO2 ratio, with CAext making little contribution. Inhibiting the AE protein led to a 55%-65% decrease in photosynthetic rates. Inhibiting both the AE protein and CAext at pHT 9.00 led to 80%-100% inhibition of photosynthesis, whereas at pHT 7.65, passive CO2 diffusion supported 33% of photosynthesis. CAint was active at pHT 7.65 and 9.00, and activity was always higher than CAext, because of its role in dehydrating HCO3- to supply CO2 to RuBisCO. Interestingly, the main mechanism of HCO3- uptake in M. pyrifera was different than that in other Laminariales studied (CAext-catalyzed reaction) and we suggest that species-specific knowledge of carbon uptake mechanisms is required in order to elucidate how seaweeds might respond to future changes in HCO3-:CO2 due to ocean acidification.
    Keywords: Alkalinity, total; Aragonite saturation state; Aromoana; Benthos; Bicarbonate ion; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Calculated using SWCO2 (Hunter, 2007); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Carbonic anhydrase activity; Carbonic anhydrase activity, standard error; Chromista; Coast and continental shelf; Coulometric titration; EXP; Experiment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Inhibition of net photosynthesis; Inhibition of net photosynthesis, standard error; Laboratory experiment; Macroalgae; Macrocystis pyrifera; Net photosynthesis rate, oxygen; Net photosynthesis rate, oxygen, standard error; OA-ICC; Ocean Acidification International Coordination Centre; Ochrophyta; Other metabolic rates; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; Potentiometric titration; Primary production/Photosynthesis; Salinity; Single species; South Pacific; Species; Spectrophotometric; Temperate; Temperature, water
    Type: Dataset
    Format: text/tab-separated-values, 465 data points
    Location Call Number Limitation Availability
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  • 2
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    PANGAEA
    In:  Supplement to: Roleda, Michael Y; Morris, Jaz N; McGraw, Christina M; Hurd, Catriona L (2011): Ocean acidification and seaweed reproduction: increased CO2 ameliorates the negative effect of lowered pH on meiospore germination in the giant kelp Macrocystis pyrifera (Laminariales, Phaeophyceae). Global Change Biology, 18(3), 854-864, https://doi.org/10.1111/j.1365-2486.2011.02594.x
    Publication Date: 2024-03-15
    Description: The worldwide effects of ocean acidification (OA) on marine species are a growing concern. In temperate coastal seas, seaweeds are dominant primary producers that create complex habitats and supply energy to higher trophic levels. Studies on OA and macroalgae have focused on calcifying species and adult stages but, critically, they have overlooked the microscopic stages of the reproductive life cycle, which, for other anthropogenic stress e.g. UV-B radiation, are the most susceptible life-history phase. Also, environmental cues and stressors can cause changes in the sex ratio which has implications for the mating system and recruitment success. Here, we report the effects of pH (7.59-8.50) on meiospore germination and sex determination for the giant kelp, Macrocystis pyrifera (Laminariales), in the presence and absence of additional dissolved inorganic carbon (DIC). Lowered pH (7.59-7.60, using HCl-only) caused a significant reduction in germination, while added DIC had the opposite effect, indicating that increased CO2 at lower pH ameliorates physiological stress. This finding also highlights the importance of appropriate manipulation of seawater carbonate chemistry when testing the effects of ocean acidification on photosynthetic organisms. The proportion of male to female gametophytes did not vary significantly between treatments suggesting that pH was not a primary environmental modulator of sex. Relative to the baseline (pH 8.19), gametophytes were 32% larger under moderate OA (pH 7.86) compared to their size (10% increase) under extreme OA (pH 7.61). This study suggests that metabolically-active cells can compensate for the acidification of seawater. This homeostatic function minimises the negative effects of lower pH (high H+ ions) on cellular activity. The 6-9% reduction in germination success under extreme OA suggests that meiospores of M.pyrifera may be resistant to future ocean acidification.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Benthos; Bicarbonate ion; Bicarbonate ion, standard deviation; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Calculated using SWCO2 (Hunter, 2007); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbonate ion; Carbonate ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, partial pressure, standard deviation; Chromista; Closed cell titration; Coast and continental shelf; Dihydrogen carbonate; Dihydrogen carbonate, standard deviation; 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); Identification; Laboratory experiment; Macroalgae; Macrocystis pyrifera; Macrocystis pyrifera, gametophyte size; Macrocystis pyrifera, gametophyte size, standard deviation; Macrocystis pyrifera, germination rate; Macrocystis pyrifera, germination rate, standard deviation; Macrocystis pyrifera, sex ratio; Macrocystis pyrifera, sex ratio, standard deviation; OA-ICC; Ocean Acidification International Coordination Centre; Ochrophyta; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, standard deviation; pH meter (Orion 720A); Reproduction; Salinity; Single species; South Pacific; Temperate; Temperature, water
    Type: Dataset
    Format: text/tab-separated-values, 447 data points
    Location Call Number Limitation Availability
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