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  • 1
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Widdicombe, Stephen; Beesley, A; Berge, J A; Dashfield, S L; McNeill, C L; Needham, H R; Øxnevad, S (2013): Impact of elevated levels of CO2 on animal mediated ecosystem function: The modification of sediment nutrient fluxes by burrowing urchins. Marine Pollution Bulletin, 73(2), 416-427, https://doi.org/10.1016/j.marpolbul.2012.11.008
    Publication Date: 2024-03-15
    Description: A mesocosm experiment was conducted to quantify the relationships between the presence and body size of two burrowing heart urchins (Brissopsis lyrifera and Echinocardium cordatum) and rates of sediment nutrient flux. Furthermore, the impact of seawater acidification on these relationships was determined during this 40-day exposure experiment. Using carbon dioxide (CO2) gas, seawater was acidified to pHNBS 7.6, 7.2 or 6.8. Control treatments were maintained in natural seawater (pH = 8.0). Under normocapnic conditions, burrowing urchins were seen to reduce the sediment uptake of nitrite or nitrate whilst enhancing the release of silicate and phosphate. In acidified (hypercapnic) treatments, the biological control of biogeochemical cycles by urchins was significantly affected, probably through the combined impacts of high CO2 on nitrifying bacteria, benthic algae and urchin behaviour. This study highlights the importance of considering biological interactions when predicting the consequences of seawater acidification on ecosystem function.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Ammonium, flux; Animalia; Aragonite saturation state; Behaviour; Benthic animals; Benthos; Bicarbonate ion; Bottles or small containers/Aquaria (〈20 L); Brissopsis lyrifera; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Coast and continental shelf; Comment; Echinocardium cordatum; Echinodermata; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Laboratory experiment; Mass; Mortality/Survival; Nitrate, flux; Nitrite, flux; North Atlantic; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, standard deviation; Phosphate, flux; Potentiometric; Potentiometric titration; Salinity; Salinity, standard deviation; Silicate, flux; Single species; Size; Species; Status; Temperate; Temperature, water; Temperature, water, standard deviation; Treatment
    Type: Dataset
    Format: text/tab-separated-values, 4040 data points
    Location Call Number Expected Availability
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  • 2
    Publication Date: 2024-02-16
    Description: A baseline survey of the benthic community structure in the vicinity of the Goldeneye platform, in the North Sea.
    Keywords: Abra nitida; Abyssoninoe spp.; Acanthocardia, juvenile; Acanthocardia spp.; Acidostoma sarsi; Actiniaria; Ampelisca diadema; Ampelisca gibba; Ampelisca macrocephala; Ampelisca tenuicornis; Ampharete falcata; Ampharete lindstroemi; Ampharete octocirrata; Ampharetidae, juvenile; Amphicteis gunneri; Amphictene auricoma; Amphipoda indeterminata; Amphiura, juvenile; Amphiura chiajei; Amphiura filiformis; Ancistrosyllis groenlandica; Anobothrus gracilis; Anonyx; Aonides paucibranchiata; Aphelochaeta; Aphrodita aculeata; Aphrodita aculeata, juvenile; Apistobranchus tullbergi; Arctica islandica, juvenile; Argissa hamatipes; Aricidea capensis bansei; Aricidea catherinae; Aricidea spp.; Aricidea suecica; Astacidea, juvenile; Astacilla dilatata; Astarte, juvenile; Asteroidea, larvae; Astropecten irregularis; Astropecten irregularis, juvenile; Axinulus croulinensis; baseline data; BC; Benthic; Benthic biota; Benthos; Bopyridae spp.; Box corer; Brada villosa; Brissopsis lyrifera; Brissopsis lyrifera, juvenile; Bullomorpha spp.; Bylgides spp.; Callianassa subterranea; Calocaris macandreae; Campylaspis costata; Carbon capture and storage; Caudofoveata, juvenile; CCS; Ceratocephale loveni; Cerianthus lloydii; Cerianthus lloydii, juvenile; Chaetoderma nitidulum; Chaetoparia nilssoni; Chaetopterus variopedatus; Chaetozone christiei; Cirratulidae, juvenile; Cirratulus caudatus; Cirrophorus furcatus; Clymenura spp.; Copepoda; Corbula gibba; Corophium affine; Crangon crangon; Date/Time of event; Decapoda megalopa; Decapoda spp.; Devonia perrieri; Diastylis, juvenile; Diastylis boecki; Diastylis lucifera; Diastyloides biplicatus; Diplocirrus glaucus; Dipolydora; Drilonereis spp.; Dulichia falcata; Dyopedos monacanthus; Echinoidea, juvenile; Echiurus echiurus; Eclysippe vanelli; Edwardsia spp.; Elevation of event; Enipo elisabethae; Ennucula tenuis; Ericthonius brasiliensis; Eriopisa elongata; Euclymene; Eudorella emarginata; Eudorella truncatula; Eugerda; Eurydice pulchra; Eurydice spinigera; Euspira catena; Euspira fusca; Event label; Exogone hebes; Fabricia; Falcidens crossotus; Fibulariidae, juvenile; Fishing intensity; Galathea strigosa; Galathowenia oculata; Gari, juvenile; Gattyana cirrhosa; Glycera alba; Glycera tridactyla; Glycinde nordmanni; Gnathia oxyuraea; Gnathia praniza; Goldeneye; Golfingia elongata; Goniada maculata; Goniada maculata, juvenile; Goniada pallida; Goniadidae, juvenile; Haploops tubicola; Hardametopa nasuta; Harmothoe antilopes; Harmothoe glabra; Harpinia antennaria; Harpinia laevis; Harpinia pectinata; Heteromastus filiformis; Hiatella arctica; Hormathia digitata; Hydrozoa; Hypereteone foliosa; Hyperiidea; Iphinoe trispinosa; Isaeidae, female; Jassa marmorata; Lanice conchilega; Laonice; Laonice, juvenile; Laonice appelloefi; Laonice bahusiensis; Laonice sarsi; Latitude of event; Lembos longipes; Leptosynapta spp.; Leucon acutirostris; Levinsenia gracilis; Limatula subauriculata; Liocarcinus pusillus; Longitude of event; Lucinoma borealis; Lumbrineris spp.; Lysilla loveni; Macrochaeta; Macrofauna; Mactra, juvenile; Maera loveni; Maldanidae, juvenile; Malmgrenia arenicolae; Marphysa bellii; Melinnopsis spp.; Melitidae, juvenile; Mendicula ferruginosa; Minuspio cirrifera; Myodocopa; Myrtea spinifera; Myxine glutinosa; Nematoda; Nemertea; Nephtys, juvenile; Nephtys assimilis; Nephtys hombergii; Nephtys hystricis; Nephtys kersivalensis; Nephtys paradoxa; Nereis longissima; Nicippe tumida; North Sea; Notomastus; Nuculana minuta; Nucula nucleus; Nucula sulcata; Nudibranchia; Oediceros borealis; Onoba semicostata; Opheliidae, juvenile; Ophelina abranchiata; Ophelina acuminata; Ophelina cylindricaudata; Ophelina norvegica; Ophiocten affinis; Ophiodromus flexuosus; Ophiura, juvenile; Ophryotrocha puerilis; Orbinia sertulata; Orchomene nana; Ostracoda; Owenia fusiformis; Panthalis oerstedi; Paradoneis lyra; Paralamprops orbicularis; Paramphinome jeffreysii; Paramphitrite tetrabranchia; Pariambus typicus; Pennatula phosphorea; Peresiella clymenoides; Perioculodes longimanus; Perophora spp.; Perrierella audouiniana; Phaxas pellucidus, juvenile; Philocheras bispinosus; Philocheras trispinosus; Pholoe baltica; Phoronis; Phtisica marina; Phyllodoce longipes; Phyllodocidae spp.; Phylo norvegicus; Pista cristata; Platyhelminthes; Pockmark; Podarkeopsis capensis; Polycirrus spp.; Polydora caulleryi; Polydora flava; POS527; POS527_100-1; POS527_101-1; POS527_105-1; POS527_106-1; POS527_108-1; POS527_109-1; POS527_110-1; POS527_11-1; POS527_112-1; POS527_113-1; POS527_12-1; POS527_125-1; POS527_126-1; POS527_127-1; POS527_128-1; POS527_130-1; POS527_13-1; POS527_131-1; POS527_132-1; POS527_133-1; POS527_134-1; POS527_135-1; POS527_14-1; POS527_16-1; POS527_17-1; POS527_19-1; POS527_20-1; POS527_22-1; POS527_23-1; POS527_24-1; POS527_26-1; POS527_28-1; POS527_29-1; POS527_30-1; POS527_35-1; POS527_36-1; POS527_37-1; POS527_38-1; POS527_39-1; POS527_40-1; POS527_41-1; POS527_42-1; POS527_44-1; POS527_45-1; POS527_48-1; POS527_49-1; POS527_50-1; POS527_52-1; POS527_53-1; POS527_54-1; POS527_55-1; POS527_56-1; POS527_57-1; POS527_58-1; POS527_59-1; POS527_6-1; POS527_61-1; POS527_73-1; POS527_74-1; POS527_75-1; POS527_76-1; POS527_78-1; POS527_79-1; POS527_80-1; POS527_8-1; POS527_81-1; POS527_82-1; POS527_83-1; POS527_84-1; POS527_85-1; POS527_86-1; POS527_95-1; POS527_97-1; POS527_98-1; POS527_99-1; Poseidon; Praxillella affinis; Praxillura longissima; Priapulus caudatus; Prionospio fallax; Prionospio spp.; Prionospio steenstrupi; Protomedeia fasciata; Psamathe fusca; Pseudopolydora paucibranchiata; Rhizorus acuminatus; Rhodine loveni; Sabellidae spp.; Sagitta spp.; Sample code/label; Sample ID; Scaphander lignarius, juvenile; Schistomeringos caeca; Scolelepis spp.; Scoletoma spp.; Scoloplos armiger; Scutopus ventrolineatus; Sediment type; Siboglinum spp.; Sige fusigera; Sipuncula spp.; Spatangoida, juvenile; Spiochaetopterus typicus; Spionidae; Spiophanes bombyx; Spiophanes kroyeri; STEMM-CCS; Sthenelais limicola; Strategies for Environmental Monitoring of Marine Carbon Capture and Storage; Streblosoma intestinale; Synchelidium haplocheles; Synchelidium maculatum; Synelmis klatti; Tanaidacea spp.; Tellimya ferruginosa; Terebellides stroemii; Tharyx; Thracia; Thracia, juvenile; Thyasira flexuosa; Thyasira polygona; Thyasira sarsii; Thyasiridae, juvenile; Timoclea, juvenile; Timoclea ovata; Tiron spiniferus; Trichobranchus glacialis; Tubificoides amplivasatus; Urothoe elegans; Urothoe marina; Virgularia mirabilis; Virgularia mirabilis, juvenile; Well; Westwoodilla caecula
    Type: Dataset
    Format: text/tab-separated-values, 20512 data points
    Location Call Number Expected Availability
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  • 3
    Publication Date: 2024-03-15
    Description: The geological storage of carbon dioxide (CO2) is expected to be an important component of future global carbon emission mitigation, but there is a need to understand the impacts of a CO2 leak on the marine environment and to develop monitoring protocols for leakage detection. In the present study, sediment cores were exposed to CO2-acidified seawater at one of five pH levels (8.0, 7.5, 7.0, 6.5 and 6.0) for 10 weeks. A bloom of Spirulina sp. and diatoms appeared on sediment surface exposed to pH 7.0 and 7.5 seawater. Quantitative PCR measurements of the abundance of 16S rRNA also indicated an increase to the abundance of microbial 16S rRNA within the pH 7.0 and 7.5 treatments after 10 weeks incubation. More detailed analysis of the microbial communities from the pH 7.0, 7.5 and 8.0 treatments confirmed an increase in the relative abundance of Spirulina sp. and Navicula sp. sequences, with changes to the relative abundance of major archaeal and bacterial groups also detected within the pH 7.0 treatment. A decreased flux of silicate from the sediment at this pH was also detected. Monitoring for blooms of microphytobenthos may prove useful as an indicator of CO2 leakage within coastal areas.
    Keywords: 16S gene copy number per unit sediment mass; Alkalinity, total; Ammonia; Aragonite saturation state; Benthos; Bicarbonate ion; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Coast and continental shelf; Community composition and diversity; Core; Entire community; EXP; Experiment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Identification; Laboratory experiment; Nitrate; Nitrite; North Atlantic; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; Phosphate; Salinity; Silicate; Silicate, flux; Soft-bottom community; Temperate; Temperature, water; Time in weeks; Treatment: pH; Type; Western_English_Channel
    Type: Dataset
    Format: text/tab-separated-values, 1400 data points
    Location Call Number Expected Availability
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  • 4
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Christen, Nadja; Calosi, Piero; McNeill, C L; Widdicombe, Stephen (2012): Structural and functional vulnerability to elevated pCO2 in marine benthic communities. Marine Biology, 160(8), 2113-2128, https://doi.org/10.1007/s00227-012-2097-0
    Publication Date: 2024-03-15
    Description: The effect of elevated pCO2/low pH on marine invertebrate benthic biodiversity, community structure and selected functional responses which underpin ecosystem services (such as community production and calcification) was tested in a medium-term (30 days) mesocosm experiment in June 2010. Standardised intertidal macrobenthic communities, collected (50.3567°N, 4.1277°W) using artificial substrate units (ASUs), were exposed to one of seven pH treatments (8.05, 7.8. 7.6, 7.4, 7.2, 6.8 and 6.0). Community net calcification/dissolution rates, as well as changes in biomass, community structure and diversity, were measured at the end of the experimental period. Communities showed significant changes in structure and reduced diversity in response to reduced pH: shifting from a community dominated by calcareous organisms to one dominated by non-calcareous organisms around either pH 7.2 (number of individuals and species) or pH 7.8 (biomass). These results were supported by a reduced total weight of CaCO3 structures in all major taxa at lowered pH and a switch from net calcification to net dissolution around pH 7.4 (Omega calc = 0.78, Omega ara = 0.5). Overall community soft tissue biomass did not change with pH and high mortality was observed only at pH 6.0, although molluscs and arthropods showed significant decreases in soft tissue. This study supports and refines previous findings on how elevated pCO2 can induce changes in marine biodiversity, underlined by differential vulnerability of different phyla. In addition, it shows significant elevated pCO2-/low pH-dependent changes in fundamental community functional responses underpinning changes in ecosystem services.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Aragonite saturation state, standard deviation; Benthos; Bicarbonate ion; Bicarbonate ion, standard deviation; Biomass, wet mass; Biomass/Abundance/Elemental composition; Bottles or small containers/Aquaria (〈20 L); Calcification/Dissolution; Calcite saturation state; Calcite saturation state, standard deviation; Calcium carbonate, mass; 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; Coast and continental shelf; Community composition and diversity; Description; Entire community; Evenness of species; EXP; Experiment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Identification; Laboratory experiment; Mount_Batten; Net calcification rate of calcium carbonate; North Atlantic; Number of calcareous individuals; Number of calcareous species; Number of individuals; Number of non-calcareous individuals; Number of non-calcareous species; Number of species; OA-ICC; Ocean Acidification International Coordination Centre; Organisms, calcareous, biomass; Organisms, non-calcareous, biomass; Oxygen; Oxygen, standard deviation; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; Potentiometric; Potentiometric titration; Rocky-shore community; Salinity; Salinity, standard deviation; Soft tissue, mass; Temperate; Temperature, standard deviation; Temperature, water; Treatment
    Type: Dataset
    Format: text/tab-separated-values, 6573 data points
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  • 5
  • 6
  • 7
    Publication Date: 2012-11-18
    Print ISSN: 0025-3162
    Electronic ISSN: 1432-1793
    Topics: Biology
    Published by Springer
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  • 8
    Publication Date: 2014-05-28
    Description: A mesocosm experiment was conducted to quantify the relationships between the presence and body size of two burrowing heart urchins (Brissopsis lyrifera and Echinocardium cordatum) and rates of sediment nutrient flux. Furthermore, the impact of seawater acidification on these relationships was determined during this 40-day exposure experiment. Using carbon dioxide (CO2) gas, seawater was acidified to pHNBS 7.6, 7.2 or 6.8. Control treatments were maintained in natural seawater (pH ≈ 8.0). Under normocapnic conditions, burrowing urchins were seen to reduce the sediment uptake of nitrite or nitrate whilst enhancing the release of silicate and phosphate. In acidified (hypercapnic) treatments, the biological control of biogeochemical cycles by urchins was significantly affected, probably through the combined impacts of high CO2 on nitrifying bacteria, benthic algae and urchin behaviour. This study highlights the importance of considering biological interactions when predicting the consequences of seawater acidification on ecosystem function. Highlights: ► At pH8, urchins reduced sediment uptake of NOx and increased the release of silicate and phosphate. ► Reduced pH significantly affected the relationship between urchins and sediment nutrient fluxes. ► CCS leaks could alter nutrient cycling by disrupting key animal–microbial relationships.
    Type: Article , PeerReviewed
    Format: text
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