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  • 2010-2014  (80)
  • 1990-1994  (35)
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  • 1
    Online Resource
    Online Resource
    Berlin/Boston :De Gruyter, Inc.,
    Keywords: Marine algae -- Polar Regions. ; Benthic plants -- Polar Regions. ; Electronic books.
    Description / Table of Contents: In-depth knowledge about aquatic plant species, from their sub-cellular organization to their interactions within ecosystems, is of utmost importance as the world faces the challenges of the 21st century. From losses in biodiversity and changes in aquatic ecosystems to the potential of algal biofuel and artificial photosynthesis, some of the hottest topics of our time rely on basic research in aquatic botany. This new book series covers topics from all of the disciplines of marine and freshwater botany at all levels of biological organization. Primary subject areas are: systematics, floristics, biogeography, ecology, biochemistry, molecular biology, genetics, chemistry, industrial processes and utilization, and biotechnology of algae and angiosperms. Mycology and microbiology topics are also part of the scope of the series.
    Type of Medium: Online Resource
    Pages: 1 online resource (351 pages)
    Edition: 1st ed.
    ISBN: 9783110229714
    Series Statement: Marine and Freshwater Botany Series
    DDC: 579.8/17760911
    Language: English
    Note: Frontmatter -- Contents -- 1. Introduction. Biology of polar benthic algae -- 2. The abiotic environment of polar marine benthic algae -- 3. Biodiversity, biogeography and zonation of marine benthic micro- and macroalgae in the Arctic and Antarctic -- 4. Notes on the systematics and biogeographical relationships of Antarctic and sub-Antarctic Rhodophyta with descriptions of four new genera and five new species -- 5. Defenses of polar macroalgae against herbivores and biofoulers -- 6. Field studies on deterrent properties of phlorotannins in Antarctic brown algae -- 7. Benthic microalgal production in the Arctic: applied methods and status of the current database -- 8. Microphytobenthic biomass along gradients of physical conditions in Arctic Kongsfjorden, Svalbard -- 9. Phenology and seasonal physiological performance of polar seaweeds -- 10. Light and temperature demands of marine benthic microalgae and seaweeds in polar regions -- 11. Freezing tolerance and photosynthetic performance of polar seaweeds at low temperatures -- 12. Impact of oceanic warming on the distribution of seaweeds in polar and cold-temperate waters -- 13. Physiological responses of polar benthic algae to ultraviolet radiation -- 14. Drivers of colonization and succession in polar benthic macro- and microalgal communities -- 15. Conclusion and outlook. Future perspectives on the investigation of polar benthic algae -- Backmatter.
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  • 2
    Online Resource
    Online Resource
    Berlin, Heidelberg :Springer Berlin / Heidelberg,
    Keywords: Marine biology. ; Electronic books.
    Description / Table of Contents: This book covers all aspects of seaweed: acclimation in the abiotic environment, biotic interactions in seaweed communities, structure and function of seaweed systems, environmental changes and seaweed aquaculture. Includes industrial and economic aspects.
    Type of Medium: Online Resource
    Pages: 1 online resource (507 pages)
    Edition: 1st ed.
    ISBN: 9783642284519
    Series Statement: Ecological Studies ; v.219
    DDC: 579.88
    Language: English
    Note: Intro -- Seaweed Biology -- Novel Insights into Ecophysiology, Ecology and Utilization -- Preface -- Contents -- Part I: Fundamental Processes and Acclimation to Abiotic Environmental Variables -- Chapter 1: Physiological and Photomorphogenic Effects of Light on Marine Macrophytes -- 1.1 Introduction -- 1.2 Photosynthesis Under Limiting Light Conditions -- 1.3 Photosynthesis Under Excessive Light Conditions -- 1.4 Effect of Ultraviolet Radiation on Zonation of Macroalgae -- 1.5 Light Absorption and Light Spectrum -- 1.6 Light as an Environmental Signal -- 1.7 Conclusive Remarks -- References -- Chapter 2: Morpho-functionality of Carbon Metabolism in Seaweeds -- 2.1 Introduction -- 2.2 Inorganic Carbon Acquisition -- 2.3 Photosynthetic Carbon Fixation -- 2.3.1 Calvin-Benson Cycle and RUBISCO -- 2.3.2 Rates of Carbon Fixation -- 2.3.3 Photorespiration -- 2.4 Light-Independent Carbon Fixation -- 2.5 Morpho-functional Aspects of Carbon Metabolism -- 2.5.1 The Role of Storage Carbohydrates -- 2.5.2 Thallus Anatomy and Long-Distance Transport of Photoassimilates -- 2.5.3 Patterns of Carbon Allocation -- 2.5.4 Concluding Remarks -- References -- Chapter 3: Seaweed Responses to Temperature -- 3.1 Introduction -- 3.2 Local Temperature Adaptation of Growth and Photosynthesis -- 3.3 Phenotypic Temperature Acclimation of Growth and Photosynthesis -- 3.4 Disruptive Temperature Stress and Thermal Tolerance -- 3.5 Temperature Control of Biogeographical Distribution Boundaries -- 3.6 Conclusion -- References -- Chapter 4: Environment and Algal Nutrition -- 4.1 Introduction -- 4.2 Meeting Nutritional Needs -- 4.2.1 Extracting Nutrients from their Environment -- 4.2.2 Neutral vs. Ionic Nutrients -- 4.2.3 N vs. P Limitation -- 4.2.4 Considering C as Just Another Nutrient -- 4.3 Uncoupling Uptake and Incorporation -- 4.4 Different Ways of N Utilization. , 4.4.1 Seaweed Diversity Linked to Nutrient Source -- 4.4.2 Slow-Growing vs. Fast-Growing Species -- 4.5 Use of Isotope Discrimination -- 4.6 Aquaculture -- 4.6.1 Nutrient Uptake at High Concentrations -- 4.7 Conclusions -- References -- Chapter 5: Seaweed Acclimation to Salinity and Desiccation Stress -- 5.1 Variability of Salinity in Seaweed Habitats -- 5.2 Effects of Salinity Stress and Desiccation on the Physiology of Seaweeds -- 5.2.1 Rate of Survival -- 5.2.2 Growth -- 5.2.3 Photosynthesis and Respiration -- 5.3 Processes of Osmotic Acclimation -- 5.3.1 Inorganic Ions -- 5.3.2 Organic Osmolytes -- 5.3.3 Biosynthesis of Organic Osmolytes -- 5.3.4 Antioxidants -- 5.3.5 Ultrastructural Changes -- 5.3.6 Self Protection -- 5.4 Salinity Ecotypes -- 5.5 Outlook -- References -- Chapter 6: Seaweed Responses to Environmental Stress: Reactive Oxygen and Antioxidative Strategies -- 6.1 Introduction -- 6.2 Stress-Induced ROS Production and Its Effects on Seaweed Performance -- 6.2.1 Seaweed Exposure to Heavy Metal Stress and Reactive Oxygen Metabolism -- 6.2.2 A Peculiar Antioxidant System in Kelp -- 6.3 Antioxidative Strategies in Seaweeds on Seasonal and Spatial Scales -- 6.3.1 SOD Activity in the Brown Seaweed Desmarestia anceps Along a Depth Gradient: A Case Study in Antarctica -- 6.3.2 Seasonal Changes in SOD Activity in Seaweeds from an Arctic Fjord -- 6.4 Oxidative Bursts: Reactive Oxygen and Interspecific Interaction -- 6.5 Summary -- References -- Part II: Biotic Interactions -- Chapter 7: Competition, a Major Factor Structuring Seaweed Communities -- 7.1 Competition Theory -- 7.2 Competition Among Marine Macroalgae -- 7.2.1 Overview -- 7.2.2 Competition for Light -- 7.2.3 Competition for Space -- 7.2.4 Competition for Nutrients -- 7.3 Competition in Complex Environments -- 7.3.1 Synergistic Effects of Different Factors. , 7.3.2 The Importance of Competition in Maintaining Marine Forests -- 7.3.3 Competition in the Face of Climate Change -- 7.4 Concluding Remarks -- References -- Chapter 8: Grazers on Benthic Seaweeds -- 8.1 Common Classification Systems of Grazers -- 8.2 Digestive Adaptations in Grazers -- 8.3 Grazer Impacts on Seaweeds and Seaweed Communities -- 8.4 Seaweed Defenses Against Grazing -- 8.5 Effects of Seaweed Chemical Defenses on Herbivores and Communities -- 8.6 Climate Change Effects on Seaweed-Herbivore Interactions -- 8.7 Conclusions -- References -- Chapter 9: Chemical Ecology of Seaweeds -- 9.1 Overview -- 9.2 Sensory Chemical Ecology -- 9.2.1 Chemical Communication -- 9.2.2 Environmental Sensing -- 9.3 Chemical Defense -- 9.3.1 Defenses Against Predation -- 9.3.2 Defenses Against Pathogens -- 9.3.3 Defenses Against Biofouling -- 9.3.4 Allelopathy -- 9.4 Outlook -- References -- Chapter 10: Bacterial Communities on Macroalgae -- 10.1 Introduction -- 10.2 Microbial Communities Associated with Macroalgae -- 10.3 Host-Specific Microbial Communities on Macroalgae? -- 10.4 A Model of Surface Colonization on Macroalgae -- 10.5 Conclusions -- References -- Chapter 11: Intimate Associations Between Epiphytes, Endophytes, and Parasites of Seaweeds -- 11.1 Introduction -- 11.2 Ecology and Biology of Close Biotic Interactions of Seaweeds -- 11.2.1 Epiphytes -- 11.2.2 Pigmented Endophytes -- 11.2.2.1 Endophytes in Red Algae -- 11.2.2.2 Endophytes in Brown Algae -- 11.2.2.3 Endophytes in Green Algae -- 11.2.2.4 Life History Stages of Seaweeds as Endophytic Filaments in Other Taxa -- Kelp Gametophytes in Red Filamentous Algae -- Green Algal Endophytes as Alternate Life History Phases of Acrosiphonia Species -- 11.2.3 Eukaryotic Parasites and Pathogens -- 11.2.3.1 Adelphoparasites and Alloparasites of Red Algae. , 11.2.3.2 Fungal and Oomycete Parasites and/or Pathogens -- 11.3 Cross-Talk Between Host and Colonizers and Defenses Against Colonization -- 11.3.1 Cross-Talk Involved in Host Colonization -- 11.3.2 ``Ménages à trois,´´ Quorum Sensing Mediated Bacterial-Macroalgal Interactions Modulate Colonization -- 11.3.3 Allelopathic Interactions and Induced Defenses -- 11.4 Impacts of Close Associations -- 11.4.1 Community Context -- 11.4.2 Implications to Seaweed Mariculture -- 11.4.3 Fouling -- 11.5 Summary and Prospects -- References -- Chapter 12: Invasive Marine Seaweeds: Pest or Prize? -- 12.1 Introduction -- 12.2 Biological Traits of Invasive Seaweeds -- 12.2.1 Seaweed Invasions Are Mostly Human-Mediated -- 12.3 The Identification of Introduced Seaweeds Is Not Always Easy -- 12.3.1 Relevant Taxonomic Units in Seaweeds Molecular Ecology -- 12.3.2 Case Study: Sargassum Muticum -- 12.3.3 Case Study: Undaria Pinnatifida -- 12.3.4 Case Study: Asparagopsis Armata -- 12.3.5 Case Study: Asparagopsis Taxiformis -- 12.3.6 Case Study: Codium Fragile ssp. Tomentosoides -- 12.3.7 Case Study: Caulerpa spp. -- 12.3.8 Assessing Seaweed Introductions -- 12.4 Are Introduced Species a Pest or Prize? A Crab´s Tale -- 12.4.1 Commercially Used Invasive Seaweeds -- 12.4.2 Gracilaria salicornia -- 12.4.3 Eucheuma and Kappaphycus spp. -- 12.4.4 Asparagopsis Species -- 12.4.5 Caulerpa Species -- 12.4.6 Ulva Species -- 12.4.7 Undaria pinnatifida -- 12.4.8 Codium Fragile Subspecies Tomentosoides -- 12.5 Conclusions -- References -- Part III: Structure and Function of the World´s Main Seaweed Systems -- Chapter 13: Seaweeds and Their Communities in Polar Regions -- 13.1 Introduction -- 13.2 Biodiversity and Biogeographical Relationships of Antarctic and Arctic Seaweeds -- 13.3 Physiological Adaptations to the Environment -- 13.3.1 Seasonal Development and Physiological Performance. , 13.3.2 Radiation Climate and Depth Zonation -- 13.3.3 Temperature Requirements and Geographic Distribution -- 13.3.4 Effect of Salinity, Temperature, and Desiccation on Supra- and Eulittoral Seaweeds -- 13.4 Ecology of Polar Seaweed Communities -- 13.4.1 Biomass, Depth Distribution, and Productivity -- 13.4.2 Elemental and Nutritional Content -- 13.4.3 Defenses Against Herbivory and Biofouling in Polar Seaweeds -- 13.4.4 Trophic Interactions -- 13.5 Impact of Global Climate Changes on Seaweeds and Their Communities -- 13.6 Conclusion -- References -- Chapter 14: Cold-Temperate Seaweed Communities of the Southern Hemisphere -- 14.1 The Regions and Their Basic Abiotic Conditions -- 14.1.1 Southwestern South America Region -- 14.1.2 Southeastern South America Region -- 14.1.3 Victoria-Tasmania Region -- 14.1.4 Southern New Zealand Region -- 14.1.5 Sub-Antarctic Islands Region -- 14.2 Structure and Function of Seaweed Communities -- 14.2.1 Southwestern South America Region (Chile) -- 14.2.2 Southeastern South America Region (Argentinean Patagonia) -- 14.2.3 Victoria-Tasmania Region -- 14.2.4 Southern New Zealand Region -- 14.2.5 Sub-Antarctic Islands Region -- 14.3 Biogeographical Processes -- 14.3.1 Cold-Temperate Kelps as Biogeographical Models -- 14.4 Major Differences with Cold Temperate Regions of the Northern Hemisphere -- 14.5 Concluding Remarks -- References -- Chapter 15: Warm Temperate Seaweed Communities: A Case Study of Deep Water Kelp Forests from the Alboran Sea (SW Mediterranean Sea) and the Strait of Gibraltar -- 15.1 Introduction: Kelp Forests and Kelp Beds in the Alboran Sea and the Strait of Gibraltar -- 15.2 Abiotic Factors Affecting Distribution of Kelps in the Alboran Sea and the Strait of Gibraltar -- 15.2.1 Substratum -- 15.2.2 Hydrodynamics -- 15.2.3 Irradiance -- 15.2.4 Temperature -- 15.2.5 Inorganic Nutrients. , 15.3 Growth and Reproduction.
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  • 3
    Type of Medium: Book
    Pages: XIV, 514 S. in 1 Teil , 235 mm x 155 mm, 801 g
    Edition: Aufl. 2012
    ISBN: 3642442145 , 9783642442148
    Series Statement: Ecological Studies 219
    DDC: 570
    Language: English
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  • 4
    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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  • 5
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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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  • 6
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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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  • 7
    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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  • 8
    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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  • 9
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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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  • 10
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    PANGAEA
    In:  Supplement to: Gutow, Lars; Rahman, Mohammed Mofizur; Bartl, Kevin; Saborowski, Reinhard; Bartsch, Inka; Wiencke, Christian (2014): Ocean acidification affects growth but not nutritional quality of the seaweed Fucus vesiculosus (Phaeophyceae, Fucales). Journal of Experimental Marine Biology and Ecology, 453, 84-90, https://doi.org/10.1016/j.jembe.2014.01.005
    Publication Date: 2024-03-15
    Description: Understanding the ecological implications of global climate change requires investigations of not only the direct effects of environmental change on species performance but also indirect effects that arise from altered species interactions. We performed CO2 perturbation experiments to investigate the effects of ocean acidification on the trophic interaction between the brown seaweed Fucus vesiculosus and the herbivorous isopod Idotea baltica. We predicted faster growth of F. vesiculosus at elevated CO2-concentrations and higher carbon content of the algal tissue. We expected that I. baltica has different consumption rates on algae that have been grown at different CO2 levels and that the isopods remove surplus carbon metabolically by enhanced respiration. Surprisingly, growth of F. vesiculosus as well as the C:N-ratio of the algal tissue were reduced at high CO2-levels. The changes in the elemental composition had no effect on the consumption rates and the respiration of the herbivores. An additional experiment showed that consumption of F. vesiculosus by the isopod Idotea emarginata was independent of ocean acidification and temperature. Our results could not reveal any effects of ocean acidification on the per capita strength of the trophic interaction between F. vesiculosus and its consumers. However, reduced growth of the algae at high CO2-concentrations might reduce the capability of the seaweed to compensate losses due to intense herbivory.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Animalia; Aragonite saturation state; Arthropoda; Behaviour; Benthic animals; Benthos; Bicarbonate ion; Bicarbonate ion, standard deviation; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calculated; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon/Nitrogen ratio; Carbon/Phosphorus ratio; Carbonate ion; Carbonate ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, standard deviation; Chromista; Coast and continental shelf; Experiment; Figure; Food consumption; Fucus vesiculosus; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Idotea balthica; Idotea emarginata; Incubation duration; Laboratory experiment; Mass; Nitrogen/Phosphorus ratio; North Atlantic; OA-ICC; Ocean Acidification International Coordination Centre; Ochrophyta; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; pH, standard deviation; Phytoplankton; Potentiometric; Potentiometric titration; Replicate; Respiration; Respiration rate, oxygen; Salinity; Salinity, standard deviation; Species; Species interaction; Temperate; Temperature; Temperature, water; Treatment
    Type: Dataset
    Format: text/tab-separated-values, 8024 data points
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