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  • 1
    Publication Date: 2022-05-26
    Description: Author Posting. © The Author(s), 2010. This is the author's version of the work. It is posted here by permission of Elsevier B.V. for personal use, not for redistribution. The definitive version was published in Deep Sea Research Part II: Topical Studies in Oceanography 58 (2011): 753-763, doi:10.1016/j.dsr2.2010.10.015.
    Description: The SOLAS air-sea gas exchange experiment (SAGE) was a multiple-objective study investigating gas-transfer processes and the influence of iron fertilisation on biologically driven gas exchange in high-nitrate low-silicic acid low-chlorophyll (HNLSiLC) Sub-Antarctic waters characteristic of the expansive Subpolar Zone of the southern oceans. This paper provides a general introduction and summary of the main experimental findings. The release site was selected from a pre-voyage desktop study of environmental parameters to be in the south-west Bounty Trough (46.5°S 172.5°E) to the south-east of New Zealand and the experiment conducted between mid-March and mid-April 2004. In common with other mesoscale iron addition experiments (FeAX’s), SAGE was designed as a Lagrangian study quantifying key biological and physical drivers influencing the air-sea gas exchange processes of CO2, DMS and other biogenic gases associated with an iron-induced phytoplankton bloom. A dual tracer SF6/3He release enabled quantification of both the lateral evolution of a labelled volume (patch) of ocean and the air-sea tracer exchange at the 10’s of km’s scale, in conjunction with the iron fertilisation. Estimates from the dual-tracer experiment found a quadratic dependency of the gas exchange coefficient on windspeed that is widely applicable and describes air-sea gas exchange in strong wind regimes. Within the patch, local and micrometeorological gas exchange process studies (100 m scale) and physical variables such as near-surface turbulence, temperature microstructure at the interface, wave properties, and wind speed were quantified to further assist the development of gas exchange models for high-wind environments. There was a significant increase in the photosynthetic competence (Fv/Fm) of resident phytoplankton within the first day following iron addition, but in contrast to other FeAX’s, rates of net primary production and column-integrated chlorophyll a concentrations had only doubled relative to the unfertilised surrounding waters by the end of the experiment. After 15 days and four iron additions totalling 1.1 tonne Fe2+, this was a very modest response compared to the other mesoscale iron enrichment experiments. An investigation of the factors limiting bloom development considered co- limitation by light and other nutrients, the phytoplankton seed-stock and grazing regulation. Whilst incident light levels and the initial Si:N ratio were the lowest recorded in all FeAX’s to date, there was only a small seed-stock of diatoms (less than 1% of biomass) and the main response to iron addition was by the picophytoplankton. A high rate of dilution of the fertilised patch relative to phytoplankton growth rate, the greater than expected depth of the surface mixed layer and microzooplankton grazing were all considered as factors that prevented significant biomass accumulation. In line with the limited response, the enhanced biological draw-down of pCO2 was small and masked by a general increase in pCO2 due to mixing with higher pCO2 waters. The DMS precursor DMSP was kept in check through grazing activity and in contrast to most FeAX’s dissolved dimethylsulfide (DMS) concentration declined through the experiment. SAGE is an important low-end member in the range of responses to iron addition in FeAX’s. In the context of iron fertilisation as a geoengineering tool for atmospheric CO2 removal, SAGE has clearly demonstrated that a significant proportion of the low iron ocean may not produce a phytoplankton bloom in response to iron addition.
    Description: SAGE was jointly funded through the New Zealand Foundation for Research, Science and Technology (FRST) programs (C01X0204) "Drivers and Mitigation of Global Change" and (C01X0223) "Ocean Ecosystems: Their Contribution to NZ Marine Productivity." Funding was also provided for specific collaborations by the US National Science Foundation from grants OCE-0326814 (Ward), OCE-0327779 (Ho), and OCE 0327188 OCE-0326814 (Minnett) and the UK Natural Environment Research Council NER/B/S/2003/00282 (Archer). The New Zealand International Science and Technology (ISAT) linkages fund provided additional funding (Archer and Ziolkowski), and the many collaborator institutions also provided valuable support.
    Keywords: Air-sea gas exchange ; Iron fertilisation ; Ocean biogeochemistry ; SOLAS
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
    Format: application/pdf
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  • 2
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    PANGAEA
    In:  Supplement to: Croot, Peter L; Bowie, Andrew R; Frew, Russell; Maldonado, Maria T; Hall, Julie A; Safi, Karl A; La Roche, Julie; Boyd, Philip W; Law, Cliff S (2001): Retention of dissolved iron and Fe II in an iron induced Southern Ocean phytoplankton bloom. Geophysical Research Letters, 28(18), 3425-3428, https://doi.org/10.1029/2001GL013023
    Publication Date: 2023-01-13
    Description: During the 13 day Southern Ocean Iron RE-lease Experiment (SOIREE), dissolved iron concentrations decreased rapidly following each of three iron-enrichments, but remained high (〉1 nM, up to 80% as FeII) after the fourth and final enrichment on day 8. The former trend was mainly due to dilution (spreading of iron-fertilized waters) and particle scavenging. The latter may only be explained by a joint production-maintenance mechanism; photoreduction is the only candidate process able to produce sufficiently high FeII, but as such levels persisted overnight (8 hr dark period) -ten times the half-life for this species- a maintenance mechanism (complexation of FeII) is required, and is supported by evidence of increased ligand concentrations on day 12. The source of these ligands and their affinity for FeII is not known. This retention of iron probably permitted the longevity of this bloom raising fundamental questions about iron cycling in HNLC (High Nitrate Low Chlorophyll) Polar waters.
    Keywords: Comment; Date/Time of event; DEPTH, water; Error; Event label; GOFLO; Go-Flo bottles; Iron, dissolved; Iron, dissolved, conditional complex stability; Iron-binding ligand, dissolved; Latitude of event; Longitude of event; SOIREE; Southern Ocean - Australasian-Pacific Sector; T1136-1; T1139-1; T1140-6; T1141-6; T1144-6; T1151-5; T1152-5; T1158-5; T1159-6; T1160-3; T1162-4; T1171-5; Tangaroa; Voltammetry
    Type: Dataset
    Format: text/tab-separated-values, 64 data points
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  • 3
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    Unknown
    PANGAEA
    In:  Supplement to: Hall, Julie A; Safi, Karl A (2001): The impact of in situ Fe fertilisation on the microbial food web in the Southern Ocean. Deep Sea Research Part II: Topical Studies in Oceanography, 48(11-12), 2591-2613, https://doi.org/10.1016/S0967-0645(01)00010-8
    Publication Date: 2024-02-01
    Description: During the Southern Ocean iron release experiment (SOIREE) in February 1999, the composition and dynamics of the microbial food web were studied. SOIREE was a mesoscale experiment with four infusions of Fe into the patch to elevate Fe concentrations inside the patch. During the 13 d experiment, samples were collected from the mixed layer inside and outside the patch for the enumeration of bacteria, picophytoplankton, phyto and heterotrophic nanoflagellates, ciliates, and for estimation of bacterial production and microzooplankton grazing. Inside the patch, bacterial numbers remained constant throughout SOIREE although bacterial production increased three-fold. A strong relationship between the increase in bacterial and primary production suggested that dissolved organic carbon and nitrogen, rather than Fe, potentially limited bacterial growth. The picophytoplankton population, was composed solely of eukaryotic cells and increased three-fold over the first 7 d of the experiment before decreasing to initial concentrations of approximately 4000 cells/ml. In contrast to the bacterial and picophytoplankton populations, the nanophytoflagellate population increased six-fold in numbers and 23-fold in biomass. This resulted in a three-fold increase in carbon flow through the microbial food web inside the patch by the end of the experiment. The increased carbon flow resulted in a small increase in total microzooplankton biomass. Ciliate abundances tripled and biomass, doubled; however, the ciliate population only contributed 3-10% of the microzooplankton biomass, which was dominated by the heterotrophic nanoflagellate population. The heterotrophic nanoflagellate numbers decreased three-fold by the end of the experiment; however, there was no significant change in biomass throughout the experiment. The changes in the dynamics and structure of the microbial food web during the SOIREE experiment suggest that microzooplankton grazing controlled the bacterial and possibly the picophytoplankton populations. In contrast, the nanophytoflagellates were initially controlled by the Fe concentration, with microzooplankton having an impact on the population towards the end of the experiment. The addition of Fe to a small patch of the Southern Ocean had a considerable impact on the microbial components of the food web, even though the overall importance of the microbial pathways decreased as a result of Fe addition.
    Keywords: JGOFS; Joint Global Ocean Flux Study
    Type: Dataset
    Format: application/zip, 14 datasets
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  • 4
    Publication Date: 2024-01-15
    Keywords: 19-Butanoyloxyfucoxanthin; 19-Hexanoyloxyfucoxanthin; 8803; 8809; 8813; 8819; 8824; 8827; 8830; 8836; 8844; 8853; Alloxanthin; Campbell Plateau Physical Oceanography; Chlorophyll a; Chlorophyll b; Chlorophyll c2; CTD/Rosette; CTD-RO; DATE/TIME; DEPTH, water; Diadinoxanthin; Divinyl chlorophyll a; Event label; Fucoxanthin; High Performance Liquid Chromatography (HPLC); HNLC; Latitude of event; Longitude of event; microscopy; Monovinyl chlorophyll a; Neoxanthin; Peridinin; pigments; Prasinoxanthin; Southern Ocean; Station label; subantarctic; TAN1702; TAN1702_12M; TAN1702_17; TAN1702_21-1; TAN1702_28; TAN1702_41; TAN1702_44; TAN1702_49; TAN1702_54; TAN1702_58; TAN1702_64; Tangaroa; Violaxanthin; Zeaxanthin
    Type: Dataset
    Format: text/tab-separated-values, 340 data points
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  • 5
    Publication Date: 2024-01-15
    Keywords: 8801; 8802; 8803; 8804; 8805; 8806; 8807; 8808; 8809; 8810; 8811; 8812; 8813; 8814; 8815; 8816; 8817; 8818; 8819; 8820; 8821; 8822; 8823; 8824; 8825; 8826; 8827; 8828; 8829; 8830; 8831; 8832; 8833; 8834; 8835; 8836; 8837; 8838; 8839; 8840; 8841; 8842; 8843; 8844; 8845; 8846; 8847; 8848; 8849; 8850; 8851; 8852; 8853; 8854; 8855; 8856; 8857; 8858; Campbell Plateau Physical Oceanography; Cast number; CTD/Rosette; CTD-RO; DATE/TIME; Density, sigma, in situ; Density, sigma-theta (0); DEPTH, water; Event label; Fluorescence; LATITUDE; LONGITUDE; Name; Oxygen; Radiation, photosynthetically active; Salinity; Station label; TAN1702; TAN1702_10; TAN1702_11-1; TAN1702_11-2; TAN1702_12; TAN1702_12M; TAN1702_13; TAN1702_14; TAN1702_15; TAN1702_16; TAN1702_17; TAN1702_17Jo; TAN1702_18; TAN1702_19; TAN1702_20; TAN1702_21-1; TAN1702_21-2; TAN1702_22; TAN1702_23; TAN1702_24; TAN1702_25; TAN1702_27; TAN1702_28; TAN1702_29; TAN1702_31; TAN1702_32; TAN1702_33; TAN1702_34; TAN1702_39; TAN1702_40; TAN1702_41; TAN1702_42; TAN1702_43; TAN1702_44; TAN1702_45; TAN1702_46; TAN1702_47; TAN1702_48; TAN1702_49; TAN1702_50; TAN1702_51; TAN1702_52; TAN1702_53; TAN1702_54; TAN1702_55; TAN1702_56; TAN1702_57; TAN1702_58; TAN1702_59; TAN1702_60; TAN1702_61; TAN1702_62; TAN1702_63; TAN1702_64; TAN1702_65; TAN1702_66; TAN1702_7; TAN1702_8; TAN1702_9; Tangaroa; Temperature, water; Type
    Type: Dataset
    Format: text/tab-separated-values, 787237 data points
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  • 6
    Publication Date: 2024-01-15
    Keywords: 8803; 8805; 8809; 8811; 8813; 8815; 8819; 8821; 8824; 8825; 8827; 8828; 8830; 8834; 8844; 8847; 8853; 8856; Actinoptychus sp.; Alexandrium sp.; Amphidinium sp.; Campbell Plateau Physical Oceanography; Ceratium fusus; Ceratium lineatum; Chaetoceros affinis; Chaetoceros convolutus; Chaetoceros danicus; Chaetoceros debilis; Chaetoceros decipiens; Chaetoceros didymus; Chaetoceros spp.; Chrysochromulina sp.; Coccolithophoridae; Coccolithus braarudii; Corethron criophilum; Cryptomonas spp.; CTD/Rosette; CTD-RO; Cysts indeterminata; Date/Time of event; DEPTH, water; Diatoms indeterminata; Dinoflagellate indeterminata; Dinophysis rotundata; Dinophysis sp.; Diplopsalis sp.; Distephanus speculum; Ditylum brightwellii; Eucampia zoodiacus; Event label; Fragilaria spp.; Goniodoma sp.; Guinardia flaccida; Guinardia spp.; Gymnodinium sp.; Gyrodinium sp.; Heterosigma akashiwo; HNLC; Indeterminata; Karenia sp.; Katodinium sp.; Latitude of event; Leptocylindrus danicus; Leptocylindrus mediterraneus; Longitude of event; Meuniera membranacea; microscopy; Navicula spp.; Nitzschia closterium; Nitzschia sigmaformis; Nitzschia sp.; Optical microscopy; Oxytoxum sp.; pigments; Podolampas sp.; Proboscia alata; Prorocentrum minimum; Prorocentrum sp.; Prorocentrum triestinum; Protoperidinium bipes; Protoperidinium sp.; Prymnesiophytes; Pseudo-nitzschia sp.; Pyramimonas sp.; Pyrophacus sp.; Rhizosolenia imbricata; Rhizosolenia spp.; Scrippsiella trochoidea; Skeletonema sp.; Station label; Stauroneis sp.; subantarctic; TAN1702; TAN1702_12; TAN1702_17; TAN1702_20; TAN1702_21-1; TAN1702_28; TAN1702_31; TAN1702_34; TAN1702_40; TAN1702_41; TAN1702_43; TAN1702_44; TAN1702_47; TAN1702_49; TAN1702_54; TAN1702_56; TAN1702_58; TAN1702_62; TAN1702_64; Tangaroa; Thalassionema nitzschioides; Thalassiosira minima; Thalassiosira sp.; Torodinium spp.
    Type: Dataset
    Format: text/tab-separated-values, 1278 data points
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  • 7
    Publication Date: 2024-01-15
    Keywords: 8803; 8805; 8809; 8811; 8813; 8815; 8819; 8821; 8824; 8825; 8827; 8828; 8830; 8834; 8844; 8847; 8853; 8856; Actinoptychus sp., biomass as carbon; Alexandrium sp., biomass as carbon; Amphidinium sp., biomass as carbon; Campbell Plateau Physical Oceanography; Ceratium fusus, biomass as carbon; Ceratium lineatum, biomass as carbon; Chaetoceros affinis, biomass as carbon; Chaetoceros convolutus, biomass as carbon; Chaetoceros danicus, biomass as carbon; Chaetoceros debilis, biomass as carbon; Chaetoceros decipiens, biomass as carbon; Chaetoceros didymus, biomass as carbon; Chaetoceros spp., biomass as carbon; Chrysochromulina sp., biomass as carbon; Coccolithophoridae, biomass as carbon; Coccolithus braarudii, biomass as carbon; Corethron criophilum, biomass as carbon; Cryptomonas spp., biomass as carbon; CTD/Rosette; CTD-RO; Cysts indeterminata, biomass as carbon; Date/Time of event; DEPTH, water; Diatoms indeterminata, biomass as carbon; Dinoflagellate indeterminata, biomass as carbon; Dinophysis rotundata, biomass as carbon; Dinophysis sp., biomass as carbon; Diplopsalis sp., biomass as carbon; Distephanus speculum, biomass as carbon; Ditylum brightwellii, biomass as carbon; Eucampia zoodiacus, biomass as carbon; Event label; Fragilaria spp., biomass as carbon; Goniodoma sp., biomass as carbon; Guinardia flaccida, biomass as carbon; Guinardia spp., biomass as carbon; Gymnodinium sp., biomass as carbon; Gyrodinium sp., biomass as carbon; Heterosigma akashiwo, biomass as carbon; HNLC; Indeterminata, biomass as carbon; Karenia sp., biomass as carbon; Katodinium sp., biomass as carbon; Latitude of event; Leptocylindrus danicus, biomass as carbon; Leptocylindrus mediterraneus, biomass as carbon; Longitude of event; Meuniera membranacea, biomass as carbon; microscopy; Navicula spp., biomass as carbon; Nitzschia closterium, biomass as carbon; Nitzschia sigmaformis, biomass as carbon; Nitzschia sp., biomass as carbon; Optical microscopy; Oxytoxum sp., biomass as carbon; pigments; Podolampas sp., biomass as carbon; Proboscia alata, biomass as carbon; Prorocentrum minimum, biomass as carbon; Prorocentrum sp., biomass as carbon; Prorocentrum triestinum, biomass as carbon; Protoperidinium bipes, biomass as carbon; Protoperidinium sp., biomass as carbon; Prymnesiophytes, biomass as carbon; Pseudo-nitzschia sp., biomass as carbon; Pyramimonas sp., biomass as carbon; Pyrophacus sp., biomass as carbon; Rhizosolenia imbricata, biomass as carbon; Rhizosolenia spp., biomass as carbon; Scrippsiella trochoidea, biomass as carbon; Skeletonema sp., biomass as carbon; Southern Ocean; Station label; Stauroneis sp., biomass as carbon; subantarctic; TAN1702; TAN1702_12; TAN1702_17; TAN1702_20; TAN1702_21-1; TAN1702_28; TAN1702_31; TAN1702_34; TAN1702_40; TAN1702_41; TAN1702_43; TAN1702_44; TAN1702_47; TAN1702_49; TAN1702_54; TAN1702_56; TAN1702_58; TAN1702_62; TAN1702_64; Tangaroa; Thalassionema nitzschioides, biomass as carbon; Thalassiosira minima, biomass as carbon; Thalassiosira sp., biomass as carbon; Torodinium spp., biomass as carbon
    Type: Dataset
    Format: text/tab-separated-values, 1278 data points
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  • 8
    Publication Date: 2024-01-15
    Keywords: 8803; 8805; 8809; 8811; 8813; 8815; 8819; 8821; 8824; 8825; 8827; 8828; 8830; 8834; 8844; 8847; 8853; 8856; Actinoptychus sp., biovolume; Alexandrium sp., biovolume; Amphidinium sp., biovolume; Campbell Plateau Physical Oceanography; Ceratium fusus, biovolume; Ceratium lineatum, biovolume; Chaetoceros affinis, biovolume; Chaetoceros convolutus, biovolume; Chaetoceros danicus, biovolume; Chaetoceros debilis, biovolume; Chaetoceros decipiens, biovolume; Chaetoceros didymus, biovolume; Chaetoceros spp., biovolume; Chrysochromulina sp., biovolume; Coccolithophoridae, biovolume; Coccolithus braarudii, biovolume; Corethron criophilum, biovolume; Cryptomonas spp., biovolume; CTD/Rosette; CTD-RO; Cysts indeterminata, biovolume; Date/Time of event; DEPTH, water; Diatoms indeterminata, biovolume; Dinoflagellate indeterminata, biovolume; Dinophysis rotundata, biovolume; Dinophysis sp., biovolume; Diplopsalis sp., biovolume; Distephanus speculum, biovolume; Ditylum brightwellii, biovolume; Eucampia zoodiacus, biovolume; Event label; Fragilaria spp., biovolume; Goniodoma sp., biovolume; Guinardia flaccida, biovolume; Guinardia spp., biovolume; Gymnodinium sp., biovolume; Gyrodinium sp., biovolume; Heterosigma akashiwo, biovolume; Indeterminata, biovolume; Karenia sp., biovolume; Katodinium sp., biovolume; Latitude of event; Leptocylindrus danicus, biovolume; Leptocylindrus mediterraneus, biovolume; Longitude of event; Meuniera membranacea, biovolume; Navicula spp., biovolume; Nitzschia closterium, biovolume; Nitzschia sigmaformis, biovolume; Nitzschia sp., biovolume; Optical microscopy; Oxytoxum sp., biovolume; Podolampas sp., biovolume; Proboscia alata, biovolume; Prorocentrum minimum, biovolume; Prorocentrum sp., biovolume; Prorocentrum triestinum, biovolume; Protoperidinium bipes, biovolume; Protoperidinium sp., biovolume; Prymnesiophytes, biovolume; Pseudo-nitzschia sp., biovolume; Pyramimonas sp., biovolume; Pyrophacus sp., biovolume; Rhizosolenia imbricata, biovolume; Rhizosolenia spp., biovolume; Scrippsiella trochoidea, biovolume; Skeletonema sp., biovolume; Station label; Stauroneis sp., biovolume; TAN1702; TAN1702_12; TAN1702_17; TAN1702_20; TAN1702_21-1; TAN1702_28; TAN1702_31; TAN1702_34; TAN1702_40; TAN1702_41; TAN1702_43; TAN1702_44; TAN1702_47; TAN1702_49; TAN1702_54; TAN1702_56; TAN1702_58; TAN1702_62; TAN1702_64; Tangaroa; Thalassionema nitzschioides, biovolume; Thalassiosira minima, biovolume; Thalassiosira sp., biovolume; Torodinium spp., biovolume
    Type: Dataset
    Format: text/tab-separated-values, 1278 data points
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  • 9
    Publication Date: 2024-01-15
    Description: The CTD and phytoplankton microscopy and pigment data deposited here were collected during a 3-week voyage on board of the New Zealand R/V Tangaroa to the Campbell Plateau located in subantarctic waters southeast of NZ. In addition to the CTD profiles we are providing High Pressure Liquid Chromatography data of phytoplankton pigments and phytoplankton community composition data obtained from optical microscopy analysis of surface mixed-layer (10 m) water samples.
    Keywords: HNLC; microscopy; pigments; Southern Ocean; subantarctic
    Type: Dataset
    Format: application/zip, 5 datasets
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  • 10
    Publication Date: 2024-02-01
    Keywords: Bacteria; Bacteria, biomass as carbon; Bacteria, production as carbon; Calculated, see reference(s); Ciliates; Ciliates, aloricate, biomass as carbon, fractionated; Ciliates, aloricate, fractionated; Ciliates, biomass as carbon; Ciliates indeterminata; Counting by flow cytometer; CTD/Rosette; CTD-RO; DEPTH, water; Inverted microscopy; JGOFS; Joint Global Ocean Flux Study; Microzooplankton, biomass as carbon; Nanoflagellates, autotrophic; Nanoflagellates, autotrophic, biomass as carbon; Nanoflagellates, autotrophic, cell biovolume; Nanoflagellates, heterotrophic; Nanoflagellates, heterotrophic, biomass as carbon; Nanoflagellates, heterotrophic, cell biovolume; Picoeukaryotes; Picoeukaryotes, biomass as carbon; see reference(s); SOIREE; Southern Ocean - Australasian-Pacific Sector; T1144-5; Tangaroa; Tintinnid; Tintinnid, biomass as carbon
    Type: Dataset
    Format: text/tab-separated-values, 120 data points
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