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  • 1
    Publication Date: 2020-06-23
    Description: Our objective for this study was to evaluate the influence of preindustrial and expected future atmospheric CO2 concentrations (280 μatm and 700 μatm pCO2, respectively) on different life-cycle stages of the kelp Laminaria hyperborea from Helgoland (Germany, North Sea). Zoospore germination, gametogenesis, vegetative growth, sorus formation and photosynthetic performance of vegetative and fertile tissue were examined. The contribution of external carbonic anhydrase (exCA) to C-supply for net-photosynthesis (net-PS) and the Chla- and phlorotannin content were investigated. Female gametogenesis and vegetative growth of sporophytes were significantly enhanced under the expected future pCO2. rETR(max) and net-PS of young vegetative sporophytes tended to increase performance at higher pCO2. The trend towards elevated net-PS vanished after inhibition of exCA. In vegetative sporophytes, phlorotannin content and Chla content were not significantly affected by pCO2.
    Type: Article , PeerReviewed
    Format: text
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  • 2
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    Oxford University Press
    In:  Journal of Experimental Botany, 64 (18). pp. 5587-5597.
    Publication Date: 2020-07-24
    Description: This study aimed to examine interactive effects between ocean acidification and temperature on the photosynthetic and growth performance of Neosiphonia harveyi. N. harveyi was cultivated at 10 and 17.5 °C at present (~380 µatm), expected future (~800 µatm), and high (~1500 µatm) pCO2. Chlorophyll a fluorescence, net photosynthesis, and growth were measured. The state of the carbon-concentrating mechanism (CCM) was examined by pH-drift experiments (with algae cultivated at 10 °C only) using ethoxyzolamide, an inhibitor of external and internal carbonic anhydrases (exCA and intCA, respectively). Furthermore, the inhibitory effect of acetazolamide (an inhibitor of exCA) and Tris (an inhibitor of the acidification of the diffusive boundary layer) on net photosynthesis was measured at both temperatures. Temperature affected photosynthesis (in terms of photosynthetic efficiency, light saturation point, and net photosynthesis) and growth at present pCO2, but these effects decreased with increasing pCO2. The relevance of the CCM decreased at 10 °C. A pCO2 effect on the CCM could only be shown if intCA and exCA were inhibited. The experiments demonstrate for the first time interactions between ocean acidification and temperature on the performance of a non-calcifying macroalga and show that the effects of low temperature on photosynthesis can be alleviated by increasing pCO2. The findings indicate that the carbon acquisition mediated by exCA and acidification of the diffusive boundary layer decrease at low temperatures but are not affected by the cultivation level of pCO2, whereas the activity of intCA is affected by pCO2. Ecologically, the findings suggest that ocean acidification might affect the biogeographical distribution of N. harveyi.
    Type: Article , PeerReviewed
    Format: text
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  • 3
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    PANGAEA
    In:  Supplement to: Olischläger, Mark; Bartsch, Inka; Gutow, Lars; Wiencke, Christian (2013): Effects of ocean acidification on growth and physiology of Ulva lactuca (Chlorophyta) in a rockpool-scenario. Phycological Research, 61(3), 180-190, https://doi.org/10.1111/pre.12006
    Publication Date: 2023-06-13
    Description: Rising atmospheric CO2-concentrations will have severe consequences for a variety of biological processes. We investigated the responses of the green alga Ulva lactuca (Linnaeus) to rising CO2-concentrations in a rockpool scenario. U. lactuca was cultured under aeraton with air containing either preindustrial pCO2 (280µatm) or for the end of the 21st century predicted (700µatm) pCO2 for 31 days. We addressed the following question: Will elevated CO2-concentrations affect photosynthesis (net photosynthesis, rETR(max), Fv/Fm, pigment composition) and growth of U. lactuca in rockpools with limited water exchange? Two phases of the experiment were distinguished: In the initial phase (day 1-4) the Seawater Carbonate System (SWCS) of the culture medium could be adjusted to the selected atmospheric pCO2 condition by continuous aeration with target pCO2 values. In the second phase (day 4-31) the SWCS was largely determined by the metabolism of the growing U. lactuca biomass. In the initial phase, Fv/Fm and rETR(max) were only slightly elevated at high CO2-concentrations whereas growth was significantly enhanced. After 31 days the Chl a content of the thalli was significantly lower under future conditions and the photosynthesis of thalli grown under preindustrial conditions was not dependent on external carbonic anhydrase. Biomass increased significantly at high CO2-concentrations. At low CO2-concentrations most adult thalli disintegrated between day 14 and 21, whereas at high CO2-concentrations most thalli remained integer until day 31. Thallus disintegration at low CO2-concentrations was mirrored in a drastic decline in seawater DIC and HCO3-. Accordingly, the SWCS differed significantly between the treatments. Our results indicated a slight enhancement of photosynthetic performance and significantly elevated growth of U. lactuca at future CO2-concentrations. The accelerated thallus disintegration at high CO2-concentrations under conditions of limited water exchange indicates additional CO2 effects on the life cycle of U. lactuca when living in rockpools.
    Keywords: AWI_Coast; BIOACID; Biological Impacts of Ocean Acidification; Coastal Ecology @ AWI
    Type: Dataset
    Format: application/zip, 2.5 MBytes
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  • 4
    Publication Date: 2023-06-13
    Keywords: Alkalinity, total; Aragonite saturation state; Benthos; Bicarbonate ion; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calculated using CO2SYS; Carbonate ion; Carbon dioxide; Chlorophyll a; Chlorophyll b; Chlorophyta; Coast and continental shelf; Date; Dry mass; Growth/Morphology; Growth rate; Identification; Incubation duration; Laboratory experiment; Macroalgae; Maximal electron transport rate, relative; Maximum photochemical quantum yield of photosystem II; Net photosynthesis rate, oxygen; Net photosynthesis rate, oxygen, per chlorophyll a; North Atlantic; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; Plantae; Potentiometric; Potentiometric titration; Primary production/Photosynthesis; Replicate; Salinity; Single species; Species; Temperate; Temperature, water; Treatment; Ulva lactuca
    Type: Dataset
    Format: text/tab-separated-values, 1851 data points
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  • 5
    Publication Date: 2023-11-23
    Description: Our objective for this study was to evaluate the influence of preindustrial and expected future atmospheric CO2 concentrations (280 µatm and 700 µatm pCO2, respectively) on different life-cycle stages of the kelp Laminaria hyperborea from Helgoland (Germany, North Sea). Zoospore germination, gametogenesis, vegetative growth, sorus formation and photosynthetic performance of vegetative and fertile tissue were examined. The contribution of external carbonic anhydrase (exCA) to C-supply for net-photosynthesis (net-PS) and the Chla- and phlorotannin content were investigated. Female gametogenesis and vegetative growth of sporophytes were significantly enhanced under the expected future pCO2. rETR(max) and net-PS of young vegetative sporophytes tended to increase performance at higher pCO2. The trend towards elevated net-PS vanished after inhibition of exCA. In vegetative sporophytes, phlorotannin content and Chla content were not significantly affected by pCO2.
    Keywords: AWI_Coast; BIOACID; Biological Impacts of Ocean Acidification; Coastal Ecology @ AWI; German Bight, North Sea; Helgoland; Meeresstation Helgoland; MULT; Multiple investigations; off_Helgoland
    Type: Dataset
    Format: application/zip, 1.7 MBytes
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  • 6
    Publication Date: 2024-03-15
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Benthos; Bicarbonate ion; BIOACID; Biological Impacts of Ocean Acidification; Bottles or small containers/Aquaria (〈20 L); 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 system computation flag; Carbon dioxide; Chlorophyll a; Chromista; Coast and continental shelf; Dry mass; Fresh weight, complete; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); German Bight, North Sea; Germination rate; Growth/Morphology; Growth rate; Helgoland; Identification; Incubation duration; Inhibition of net photosynthesis; Irradiance; Irradiance, standard deviation; Laboratory experiment; Laminaria hyperborea; Life stage; Light:Dark cycle; Macroalgae; Maximal electron transport rate, relative; Maximum photochemical quantum yield of photosystem II; Meeresstation Helgoland; MULT; Multiple investigations; Net photosynthesis rate, oxygen; Net photosynthesis rate, oxygen, per chlorophyll a; North Atlantic; OA-ICC; Ocean Acidification International Coordination Centre; Ochrophyta; off_Helgoland; Oogonium formation rate; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, standard deviation; Phlorotannins; Potentiometric; Potentiometric titration; Primary production/Photosynthesis; Replicate; Reproduction; Salinity; Single species; Species; Temperate; Temperature, water; Temperature, water, standard deviation; Treatment
    Type: Dataset
    Format: text/tab-separated-values, 3079 data points
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  • 7
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    PANGAEA
    In:  Supplement to: Olischläger, Mark; Wiencke, Christian (2013): Ocean acidification alleviates low-temperature effects on growth and photosynthesis of the red alga Neosiphonia harveyi (Rhodophyta). Journal of Experimental Botany, 64(18), 5587-5597, https://doi.org/10.1093/jxb/ert329
    Publication Date: 2024-03-15
    Description: This study aimed to examine interactive effects between ocean acidification and temperature on the photosynthetic and growth performance of Neosiphonia harveyi. N. harveyi was cultivated at 10 and 17.5 °C at present (~380 µatm), expected future (~800 µatm), and high (~1500 µatm) pCO2. Chlorophyll a fluorescence, net photosynthesis, and growth were measured. The state of the carbon-concentrating mechanism (CCM) was examined by pH-drift experiments (with algae cultivated at 10 °C only) using ethoxyzolamide, an inhibitor of external and internal carbonic anhydrases (exCA and intCA, respectively). Furthermore, the inhibitory effect of acetazolamide (an inhibitor of exCA) and Tris (an inhibitor of the acidification of the diffusive boundary layer) on net photosynthesis was measured at both temperatures. Temperature affected photosynthesis (in terms of photosynthetic efficiency, light saturation point, and net photosynthesis) and growth at present pCO2, but these effects decreased with increasing pCO2. The relevance of the CCM decreased at 10 °C. A pCO2 effect on the CCM could only be shown if intCA and exCA were inhibited. The experiments demonstrate for the first time interactions between ocean acidification and temperature on the performance of a non-calcifying macroalga and show that the effects of low temperature on photosynthesis can be alleviated by increasing pCO2. The findings indicate that the carbon acquisition mediated by exCA and acidification of the diffusive boundary layer decrease at low temperatures but are not affected by the cultivation level of pCO2, whereas the activity of intCA is affected by pCO2. Ecologically, the findings suggest that ocean acidification might affect the biogeographical distribution of N. harveyi.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Aragonite saturation state, standard deviation; Benthos; Bicarbonate ion; Bicarbonate ion, standard deviation; BIOACID; Biological Impacts of Ocean Acidification; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calcite saturation state, standard deviation; 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; Chlorophyll a; Coast and continental shelf; Effective quantum yield; Electron transport rate; Experiment; Figure; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; Identification; Incubation duration; Inhibition of net photosynthesis; Irradiance; Laboratory experiment; Light saturation; Macroalgae; Mass; Maximal electron transport rate, relative; Neosiphonia harveyi; Net photosynthesis rate, oxygen; North Atlantic; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, standard deviation; Photosynthetic quantum efficiency; Plantae; Potentiometric; Potentiometric titration; Primary production/Photosynthesis; Ratio; Rhodophyta; Salinity; Salinity, standard deviation; Single species; Species; Temperature; Temperature, water; Temperature, water, standard deviation; Time in hours; Treatment; Tropical
    Type: Dataset
    Format: text/tab-separated-values, 33142 data points
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  • 8
    Publication Date: 2024-03-15
    Description: The Arctic population of the kelp Saccharina latissima differs from the Helgoland population in its sensitivity to changing temperature and CO2 levels. The Arctic population does more likely benefit from the upcoming environmental scenario than its Atlantic counterpart. The previous research demonstrated that warming and ocean acidification (OA) affect the biochemical composition of Arctic (Spitsbergen; SP) and cold-temperate (Helgoland; HL) Saccharina latissima differently, suggesting ecotypic differentiation. This study analyses the responses to different partial pressures of CO2 (380, 800, and 1500 µatm pCO2) and temperature levels (SP population: 4, 10 °C; HL population: 10, 17 °C) on the photophysiology (O2 production, pigment composition, D1-protein content) and carbon assimilation [Rubisco content, carbon concentrating mechanisms (CCMs), growth rate] of both ecotypes. Elevated temperatures stimulated O2 production in both populations, and also led to an increase in pigment content and a deactivation of CCMs, as indicated by 13C isotopic discrimination of algal biomass (εp) in the HL population, which was not observed in SP thalli. In general, pCO2 effects were less pronounced than temperature effects. High pCO2 deactivated CCMs in both populations and produced a decrease in the Rubisco content of HL thalli, while it was unaltered in SP population. As a result, the growth rate of the Arctic ecotype increased at elevated pCO2 and higher temperatures and it remained unchanged in the HL population. Ecotypic differentiation was revealed by a significantly higher O2 production rate and an increase in Chl a, Rubisco, and D1 protein content in SP thalli, but a lower growth rate, in comparison to the HL population. We conclude that both populations differ in their sensitivity to changing temperatures and OA and that the Arctic population is more likely to benefit from the upcoming environmental scenario than its Atlantic counterpart.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Antheraxanthin; Antheraxanthin, standard deviation; Antheraxanthin/chlorophyll a ratio; Antheraxanthin/chlorophyll a ratio, standard deviation; Aragonite saturation state; Aragonite saturation state, standard deviation; Arctic; Benthos; beta-Carotene; beta-Carotene, standard deviation; Beta-Carotene/chlorophyll a ratio; Beta-Carotene/chlorophyll a ratio, standard deviation; Bicarbonate ion; Bicarbonate ion, standard deviation; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calcite saturation state, standard deviation; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Calculated using seacarb after Orr et al. (2018); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbonate ion; Carbonate ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, standard deviation; Chlorophyll a, standard deviation; Chlorophyll a per unit dry mass; Chlorophyll c; Chlorophyll c, standard deviation; Chlorophyll c2/chlorophyll a ratio; Chlorophyll c2/chlorophyll a ratio, standard deviation; Chromista; Coast and continental shelf; D1 protein, relative intensity; D1 protein, relative intensity, standard deviation; De-epoxidation state; De-epoxidation state, standard deviation; Effective quantum yield; Effective quantum yield, standard deviation; Fucoxanthin; Fucoxanthin, standard deviation; Fucoxanthin/chlorophyll a ratio; Fucoxanthin/chlorophyll a ratio, standard devitation; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Fugacity of carbon dioxide in seawater, standard deviation; Growth, relative, standard deviation; Growth/Morphology; Growth rate; Isotopic fractionation, during photosynthis; Isotopic fractionation, during photosynthis, standard deviation; Laboratory experiment; Macroalgae; Net photosynthesis rate; Net photosynthesis rate, oxygen; Net photosynthesis rate, oxygen, per chlorophyll a; Net photosynthesis rate, standard deviation; North Atlantic; OA-ICC; Ocean Acidification International Coordination Centre; Ochrophyta; Other studied parameter or process; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, standard deviation; Phlorotannins; Phlorotannins, standard deviation; Pigments, accessory; Pigments, accessory, standard deviation; Pigments, accessory/chlorophyll a ratio; Pigments, accessory/chlorophyll a ratio, standard deviation; Pigments, violaxanthin-xanthophyll-cycle/chlorophyll a ratio; Pigments, violaxanthin-xanthophyll-cycle/chlorophyll a ratio, standard deviation; Polar; Potentiometric; Potentiometric titration; Primary production/Photosynthesis; Proteins, total; Proteins, total, standard deviation; Rubisco, per dry mass; Rubisco, per protein; Rubisco content per dry mass, standard deviation; Rubisco content per protein, standard deviation; Saccharina latissima; Salinity; Salinity, standard deviation; Single species; Site; Species; Temperate; Temperature; Temperature, water; Temperature, water, standard deviation; Treatment: partial pressure of carbon dioxide; Treatment: temperature; Type of study; Violaxanthin; Violaxanthin, standard deviation; Violaxanthin/chlorophyll a ratio; Violaxanthin/chlorophyll a ratio, standard deviation; Violaxanthin-xanthophyll-cycle pigments; Violaxanthin-xanthophyll-cycle pigments, standard deviation; Zeaxanthin; Zeaxanthin, standard deviation; Zeaxanthin/chlorophyll a ratio; Zeaxanthin/chlorophyll a ratio, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 1152 data points
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  • 9
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    Oxford University Press
    In:  EPIC3Journal of Experimental Botany, Oxford University Press, ISSN: 0022-0957
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
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  • 10
    Publication Date: 2017-01-30
    Description: Previous research suggested that the polar and temperate populations of the kelp Saccharina latissima represent different ecotypes. The ecotypic differentiation might also be reflected in their biochemical composition (BC) under changing temperatures and pCO2. Accordingly, it was tested if the BC of Arctic (Spitsbergen) and temperate S. latissima (Helgoland) is different and if they are differently affected by changes in temperature and pCO2. Thalli from Helgoland grown at 17 °C and 10 °C and from Spitsbergen at 10 °C and 4 °C were all tested at either 380, 800, or 1,500 latm pCO2, and total C-, total N-, protein,soluble carbohydrate, and lipid content, as well as C/Nratio were measured. At 10 °C, the Arctic population had a higher content of total C, soluble carbohydrates, and lipids, whereas the N- and protein content was lower. At the lower tested temperature, the Arctic ecotype had particularly higher contents of lipids, while content of soluble carbohydrates increased in the Helgoland population only. In Helgoland-thalli, elevated pCO2 caused a higher content of soluble carbohydrates at 17 °C but lowered the content of N and lipids and increased the C/N-ratio at 10 °C. Elevated pCO2 alone did not affect the BC of the Spitsbergen population. Conclusively, the Arctic ecotype was more resilient to increased pCO2 than the temperate one, and both ecotypes differed in their response pattern to temperature. This differential pattern is discussed in the context of the adaptation of the Arctic ecotype to low temperature and the polar night.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Format: application/pdf
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