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  • PANGAEA  (20)
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  • 1
    facet.materialart.
    Unknown
    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
    Location Call Number Limitation Availability
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  • 2
    Publication Date: 2023-07-06
    Description: The SOAP voyage examined air-sea interactions over the productive waters of the Chatham Rise, east of New Zealand onboard the RV Tangaroa (New Zealand National Institute of Water and Atmospheric Research, Wellington) from February 12 to March 7 (Law et al., 2017: doi:10.5194/acp-17-13645-2017). 23 seawater samples were collected throughout the voyage for the purpose of generating nascent SSA. Seawater samples were collected from the ocean surface during workboat operations (approximately 10 cm depth) or from the mixed layer (3 - 12 m depth, always less than the measured mixed layer depth) or deep water samples. Surface samples were collected in prewashed 5L PTFE bottles, subsurface measurements were colected in Niskin bottles onboard a CTD rosette. Nascent SSA was generated in-situ in a 0.45 m3 cylindrical polytetrafluoroethylene chamber housing four sintered glass filters with porosities between 16 and 250 μm (Cravigan et al., 2019: https://doi.org/10.5194/acp-2019-797). Dried and filtered compressed air was passed through the glass filters at a flow rate of 15.5 ± 3 L/min and resulting SSA was sampled from the headspace of the chamber. The volatility and hygroscopicity of nascent SSA was determined with a volatility and hygroscopicity tandem differential mobility analyser (VH-TDMA) (Johnson et al., 2004: doi:10.1016/j.jaerosci.2003.10.008, 2008: doi:10.1016/j.jaerosci.2008.05.005). A diffusion drier was used to dry the sample flow to 20 ± 5 % RH prior to characterisation by the VH-TDMA. The VH-TDMA used two TSI 3010 condensation particle counters. The aerosol sample flow rate for each scanning mobility particle sizer was 1 L/min, resulting in a total inlet flow of 2 L/min, the sheath flow for the pre-DMA, V-DMA and H-DMA were 11, 6 and 6 L/min, respectively. The dependence of HGF on RH at ambient temperature was measured for one water sample (workboat 9) to provide the deliquescence relative humidity (DRH). All VH-TDMA data were inverted using the TDMAinv algorithm (Gysel et al., 2009: doi:10.1016/j.jaerosci.2008.07.013). The seawater chlorophyll-a concentration was measured by filtering 2 litres of sample water onto GF/F Whatman filters, with immediate freezing in liquid nitrogen and subsequent analysis within 3 months of collection. Filters were ground and chlorophyll-a extracted in 90 % acetone with concentration determined by a calibrated fluorometer (Perkin-Elmer), with an analytical precision of 0.001 mg/m3 (Law et al., 2011: doi:10.1016/j.dsr2.2010.10.018).
    Keywords: aerosols; ccn; Chatham Rise; DATE/TIME; Depth, description; FTIR; functional groups; Humidity, relative; Humidity, relative, maximum; Humidity, relative, minimum; Hygroscopic growth factor; Hygroscopic growth factor, raw counts; hygroscopicity; IBA; ion beam; Particle, geometric median diameter; PTFE bottle, 5L; sea spray; SOAP; SOAP (Surface Ocean Aerosol Production); SSA; TAN1203; Tangaroa; TDMA; Temperature, water; volatility; Volatility-Hygroscopicity Tandem Differential Mobility Analyser (VH-TDMA); WB9
    Type: Dataset
    Format: text/tab-separated-values, 42292 data points
    Location Call Number Limitation Availability
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  • 3
    Publication Date: 2023-07-06
    Description: The SOAP voyage examined air-sea interactions over the productive waters of the Chatham Rise, east of New Zealand onboard the RV Tangaroa (New Zealand National Institute of Water and Atmospheric Research, Wellington) from February 12 to March 7 (Law et al., 2017: doi:10.5194/acp-17-13645-2017). 23 seawater samples were collected throughout the voyage for the purpose of generating nascent SSA. Seawater samples were collected from the ocean surface during workboat operations (approximately 10 cm depth) or from the mixed layer (3 - 12 m depth, always less than the measured mixed layer depth) or deep water samples. Surface samples were collected in prewashed 5L PTFE bottles, subsurface measurements were colected in Niskin bottles onboard a CTD rosette. Nascent SSA was generated in-situ in a 0.45 m3 cylindrical polytetrafluoroethylene chamber housing four sintered glass filters with porosities between 16 and 250 μm (Cravigan et al., 2019: https://doi.org/10.5194/acp-2019-797). Dried and filtered compressed air was passed through the glass filters at a flow rate of 15.5 ± 3 L/min and resulting SSA was sampled from the headspace of the chamber. Filters were collected for compositional analysis using transmission Fourier Transform Infra Red (FTIR) and Ion Beam analysis (IBA). The nascent SSA was sampled through a 1 μm sharp cut cyclone (SCC 2.229PM1, BGI Inc., Waltham, Massachusetts) and collected on Teflon filters, with the sample confined to deposit on a 10 mm circular area. Back filter blanks were used to characterise the contamination during handling, and before analysis samples were dehydrated to remove all water, including SSA hydrates, as described in (Frossard and Russell, 2012: doi:10.1021/es3032083). Filter samples underwent simultaneous particle induced X-ray emission (PIXE) and gamma ray emission (PIGE) analysis (Cohen et al., 2004: doi:10.1016/j.nimb.2004.01.043). Si was the only compound with blank measurements above the IBA detection limit. The measured S mass was used to calculate the SO4 mass, all S was assumed to be in the form of SO4. The filter exposed area (0.785 cm2) was used to convert inorganic areal concentrations into total mass. The inorganic mass (IM) was computed as the sum of Na, Mg, SO4, Cl, K, Ca, Zn, Br and Sr. The seawater chlorophyll-a concentration was measured by filtering 2 litres of sample water onto GF/F Whatman filters, with immediate freezing in liquid nitrogen and subsequent analysis within 3 months of collection. Filters were ground and chlorophyll-a extracted in 90 % acetone with concentration determined by a calibrated fluorometer (Perkin-Elmer), with an analytical precision of 0.001 mg/m3 (Law et al., 2011: doi:10.1016/j.dsr2.2010.10.018).
    Keywords: aerosols; Bromine per total inorganic mass fraction; Calcium per total inorganic mass fraction; ccn; Chatham Rise; Chloride per total inorganic mass fraction; CTD/Rosette; CTD-RO; Date/Time of event; Depth, description; DEPTH, water; Event label; FTIR; functional groups; hygroscopicity; IBA; Inorganic mass, total; ion beam; Latitude of event; Longitude of event; Magnesium per total inorganic mass fraction; Potassium per total inorganic mass fraction; PTFE bottle, 5L; sea spray; Simultaneous particle induced X-ray emission (PIXE) and gamma ray emission (PIGE) analysis; SOAP; SOAP (Surface Ocean Aerosol Production); Sodium per total inorganic mass fraction; SSA; Strontium per total inorganic mass fraction; Sulfate per total inorganic mass fraction; TAN1203; Tangaroa; TDMA; U7505; U7506; U7507; U7508; U7510; U7518; U7520; U7521; U7524; U7528; U7530; U7532; volatility; WB1; WB10; WB4; WB5; WB6; WB7; WB8; WB9; Zinc per total inorganic mass fraction
    Type: Dataset
    Format: text/tab-separated-values, 213 data points
    Location Call Number Limitation Availability
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  • 4
    Publication Date: 2023-07-06
    Description: The SOAP voyage examined air-sea interactions over the productive waters of the Chatham Rise, east of New Zealand onboard the RV Tangaroa (New Zealand National Institute of Water and Atmospheric Research, Wellington) from February 12 to March 7 (Law et al., 2017: doi:10.5194/acp-17-13645-2017). 23 seawater samples were collected throughout the voyage for the purpose of generating nascent SSA. Seawater samples were collected from the ocean surface during workboat operations (approximately 10 cm depth) or from the mixed layer (3 - 12 m depth, always less than the measured mixed layer depth) or deep water samples. Surface samples were collected in prewashed 5L PTFE bottles, subsurface measurements were colected in Niskin bottles onboard a CTD rosette. Nascent SSA was generated in-situ in a 0.45 m3 cylindrical polytetrafluoroethylene chamber housing four sintered glass filters with porosities between 16 and 250 μm (Cravigan et al., 2019: https://doi.org/10.5194/acp-2019-797). Dried and filtered compressed air was passed through the glass filters at a flow rate of 15.5 ± 3 L/min and resulting SSA was sampled from the headspace of the chamber. The volatility and hygroscopicity of nascent SSA was determined with a volatility and hygroscopicity tandem differential mobility analyser (VH-TDMA) (Johnson et al., 2004: doi:10.1016/j.jaerosci.2003.10.008, 2008: doi:10.1016/j.jaerosci.2008.05.005). A diffusion drier was used to dry the sample flow to 20 ± 5 % RH prior to characterisation by the VH-TDMA. The VH-TDMA was also used to calculate the organic volume fraction (Cravigan et al., 2019: https://doi.org/10.5194/acp-2019-797). The VH-TDMA used two TSI 3010 condensation particle counters. The aerosol sample flow rate for each scanning mobility particle sizer was 1 L/min, resulting in a total inlet flow of 2 L/min, the sheath flow for the pre-DMA, V-DMA and H-DMA were 11, 6 and 6 L/min, respectively. The SSA volatile fraction was computed by measuring the diameter of preselected SSA upon heating by a thermodenuder up to 500 degree C, in temperature increments of 5 degree C - 50 degree C. After heating the SSA hygroscopic growth factor at 90% RH was measured. All VH-TDMA data were inverted using the TDMAinv algorithm (Gysel et al., 2009: doi:10.1016/j.jaerosci.2008.07.013). The hygroscopic growth factor, semi-volatile organic volume fraction and low volatility organic volume fraction were determined as outlined in (Cravigan et al., 2019: doi:10.5194/acp-2019-797). The seawater chlorophyll-a concentration was measured by filtering 2 litres of sample water onto GF/F Whatman filters, with immediate freezing in liquid nitrogen and subsequent analysis within 3 months of collection. Filters were ground and chlorophyll-a extracted in 90 % acetone with concentration determined by a calibrated fluorometer (Perkin-Elmer), with an analytical precision of 0.001 mg/m3 (Law et al., 2011: doi:10.1016/j.dsr2.2010.10.018).
    Keywords: aerosols; Calibrated fluorometer (Perkin-Elmer); ccn; Chatham Rise; Chlorophyll a; CTD/Rosette; CTD-RO; Date/Time of event; Depth, description; DEPTH, water; Event label; FTIR; functional groups; Hygroscopic growth factor; hygroscopicity; IBA; ion beam; Latitude of event; Longitude of event; Organic volume fraction, low-volatile; Organic volume fraction, semi-volatile; Particle, geometric median diameter; PTFE bottle, 5L; Sea-salt hydrates, volume fraction; sea spray; SOAP; SOAP (Surface Ocean Aerosol Production); SSA; TAN1203; Tangaroa; TDMA; U7505; U7506; U7507; U7508; U7510; U7518; U7520; U7521; U7524; U7528; U7530; U7532; volatility; Volatility-Hygroscopicity Tandem Differential Mobility Analyser (VH-TDMA); WB1; WB10; WB4; WB5; WB6; WB7; WB8; WB9
    Type: Dataset
    Format: text/tab-separated-values, 167 data points
    Location Call Number Limitation Availability
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  • 5
    Publication Date: 2023-07-08
    Keywords: Calculated after Luo et al. (2012); CTD/Rosette; CTD-RO; CYCLOPS2002-05-19; CYCLOPS2002-05-20; CYCLOPS2002-05-21; CYCLOPS2002-05-24; CYCLOPS2002-05-25; Date/Time of event; DEPTH, water; Event label; Latitude of event; Levantine Basin; Longitude of event; MAREDAT_Diazotrophs_Collection; Nitrate; Nitrogen Fixation (C2H2 Reduction); Nitrogen fixation rate, total; Nitrogen fixation rate, whole seawater; Phosphate; Salinity; Temperature, water
    Type: Dataset
    Format: text/tab-separated-values, 30 data points
    Location Call Number Limitation Availability
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  • 6
    Publication Date: 2023-07-06
    Description: The SOAP voyage examined air-sea interactions over the productive waters of the Chatham Rise, east of New Zealand onboard the RV Tangaroa (New Zealand National Institute of Water and Atmospheric Research, Wellington) from February 12 to March 7 (Law et al., 2017: doi:10.5194/acp-17-13645-2017). 23 seawater samples were collected throughout the voyage for the purpose of generating nascent SSA. Seawater samples were collected from the ocean surface during workboat operations (approximately 10 cm depth) or from the mixed layer (3 - 12 m depth, always less than the measured mixed layer depth) or deep water samples. Surface samples were collected in prewashed 5L PTFE bottles, subsurface measurements were colected in Niskin bottles onboard a CTD rosette. Nascent SSA was generated in-situ in a 0.45 m3 cylindrical polytetrafluoroethylene chamber housing four sintered glass filters with porosities between 16 and 250 μm (Cravigan et al., 2019: https://doi.org/10.5194/acp-2019-797). Dried and filtered compressed air was passed through the glass filters at a flow rate of 15.5 ± 3 L/min and resulting SSA was sampled from the headspace of the chamber. Filters were collected for compositional analysis using transmission Fourier Transform Infra Red (FTIR) and Ion Beam analysis (IBA). The nascent SSA was sampled through a 1 μm sharp cut cyclone (SCC 2.229PM1, BGI Inc., Waltham, Massachusetts) and collected on Teflon filters, with the sample confined to deposit on a 10 mm circular area. Back filter blanks were used to characterise the contamination during handling, and before analysis samples were dehydrated to remove all water, including SSA hydrates, as described in (Frossard and Russell, 2012: doi:10.1021/es3032083). FTIR measurements were carried out according to previous marine sampling techniques (Maria et al., 2003: doi:10.1029/2003jd003703; Russell et al., 2010: doi:10.1073/pnas.0908905107). Filter blanks were under the detection limit for the FTIR. The PM1 organic mass fraction from SSA samples collected on filters was computed from the total organic mass from FTIR analysis and the inorganic mass from ion beam analysis, as in (Cravigan et al., 2019: doi:10.5194/acp-2019-797). The uncertainty in the organic mass measured using FTIR is up to 20 % (Maria et al., 2003: doi:10.1029/2003jd003703; Russell et al., 2010: doi:10.1073/pnas.0908905107). The seawater chlorophyll-a concentration was measured by filtering 2 litres of sample water onto GF/F Whatman filters, with immediate freezing in liquid nitrogen and subsequent analysis within 3 months of collection. Filters were ground and chlorophyll-a extracted in 90 % acetone with concentration determined by a calibrated fluorometer (Perkin-Elmer), with an analytical precision of 0.001 mg/m3 (Law et al., 2011: doi:10.1016/j.dsr2.2010.10.018).
    Keywords: Acid functional groups per total organic mass fraction; aerosols; Alcohol functional groups per total organic mass fraction; Alkane functional groups per total organic mass fraction; Amine functional groups per total organic mass fraction; Carbonyl functional groups per total organic mass fraction; ccn; Chatham Rise; Chlorophyll a; CTD/Rosette; CTD-RO; Date/Time of event; Depth, description; DEPTH, water; Event label; Fourier transform infrared spectroscopy (FTIR); FTIR; functional groups; hygroscopicity; IBA; ion beam; Latitude of event; Longitude of event; Organic mass, total; Organic mass fraction; PTFE bottle, 5L; sea spray; SOAP; SOAP (Surface Ocean Aerosol Production); SSA; TAN1203; Tangaroa; TDMA; U7505; U7506; U7507; U7508; U7510; U7518; U7520; U7521; U7524; U7528; U7530; U7532; volatility; WB1; WB10; WB4; WB5; WB6; WB7; WB8; WB9
    Type: Dataset
    Format: text/tab-separated-values, 174 data points
    Location Call Number Limitation Availability
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  • 7
    Publication Date: 2024-02-01
    Keywords: CT; DATE/TIME; DEPTH, water; JGOFS; Joint Global Ocean Flux Study; LATITUDE; LONGITUDE; Measured in situ; SOIREE; SOIREE-track; Southern Ocean - Australasian-Pacific Sector; Sulfur hexafluoride, SF6; Tangaroa; Underway cruise track measurements
    Type: Dataset
    Format: text/tab-separated-values, 2772 data points
    Location Call Number Limitation Availability
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  • 8
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Abraham, Edward R; Law, Cliff S; Boyd, Philip W; Lavender, Samantha J; Maldonado, Maria T; Bowie, Andrew R (2000): Importance of stirring in the development of an iron-fertilized bloom. Nature, 407(6805), 727-730, https://doi.org/10.1038/35037555
    Publication Date: 2024-02-01
    Description: The growth of populations is known to be influenced by dispersal, which has often been described as purely diffusive (Kierstead and Slobodkin, 1953; Okubo, 1980). In the open ocean, however, the tendrils and filaments of phytoplankton populations provide evidence for dispersal by stirring (Gower et al., 1980, doi:10.1038/288157a0; Holligan et al., 1993, doi:10.1029/93GB01731). Despite the apparent importance of horizontal stirring for plankton ecology, this process remains poorly characterized. Here we investigate the development of a discrete phytoplankton bloom, which was initiated by the iron fertilization of a patch of water (7 km in diameter) in the Southern Ocean (Boyd et al., 2000, doi:10.1038/35037500). Satellite images show a striking, 150-km-long bloom near the experimental site, six weeks after the initial fertilization. We argue that the ribbon-like bloom was produced from the fertilized patch through stirring, growth and diffusion, and we derive an estimate of the stirring rate. In this case, stirring acts as an important control on bloom development, mixing phytoplankton and iron out of the patch, but also entraining silicate. This may have prevented the onset of silicate limitation, and so allowed the bloom to continue for as long as there was sufficient iron. Stirring in the ocean is likely to be variable, so blooms that are initially similar may develop very differently.
    Keywords: CT; DATE/TIME; File format; File size; JGOFS; Joint Global Ocean Flux Study; Latitude of event; Longitude of event; SOIREE; SOIREE-track; Southern Ocean - Australasian-Pacific Sector; Tangaroa; Underway cruise track measurements; Uniform resource locator/link to raw data file
    Type: Dataset
    Format: text/tab-separated-values, 24 data points
    Location Call Number Limitation Availability
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  • 9
    Publication Date: 2024-02-01
    Keywords: CTD; CTD/Rosette; CTD-RO; Date/Time of event; DEPTH, water; Event label; JGOFS; Joint Global Ocean Flux Study; Latitude of event; Longitude of event; Measured in situ; Salinity; SOIREE; Southern Ocean - Australasian-Pacific Sector; Sulfur hexafluoride, SF6; T1139-4; T1140-12; T1140-14; T1140-5; T1141-11; T1144-14; T1144-15; T1144-5; T1145-4; T1147-1; T1151-12; T1151-14; T1151-4; T1152-8; T1154-3; T1157-5; T1158-11; T1158-4; T1158-6; T1159-11; T1159-12; T1159-5; T1160-4; T1162-11; T1162-3; T1162-9; T1167-2; T1167-6; T1167-7; T1167-8; T1168-10; T1171-12; T1171-4; T1171-9; Tangaroa; Temperature, water
    Type: Dataset
    Format: text/tab-separated-values, 783 data points
    Location Call Number Limitation Availability
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  • 10
    Publication Date: 2024-05-03
    Description: Here we present physico-chemical and biological data collected during 12 research cruises conducted in SW Pacific waters east of Aotearoa New Zealand between 2009 and 2017. Nutrient and chla samples were collected mainly with Niskin bottles deployed with a Seabird 9plus CTD rosette. A small fraction of the data presented were sampled also from manually deployed Niskin bottles and the RV Tangaroa Underway Flow-Through System (TUFTS) system equipped with temperature, salinity and fluorescence sensors. The dataset includes measurements of temperature, salinity, oxygen and transmissivity obtained with a Seabird 9plus; inorganic nutrients (dissolved reactive phosphorus, dissolved reactive silica, nitrate + nitrite); total chlorophyll a (chla) filtered onto GFF filter, size fractionated chla (0.2, 2, 20 microns) obtained by sequential filtration of seawater through 20, 2 and 0.2 micron polycarbonate filters; and derived mixed-layer depth estimated following temperature and density criteria. The depth of the euphotic zone included was calculated from chla concentration following the approach described in Maritorena and Morel, 2001 (doi:10.1029/2000jc000319). These data were used to provide oceanographic context to DNA metabarcoding analysis of 18S rRNA V4 region that was carried out on DNA samples collected in parallel to nutrient and chla samples. The study resulting from this analysis has been submitted to Progress in Oceanography.
    Keywords: 5806; 5809; 5819; 5829; 5833; 61TG20151203; 61TG20160509; 61TG20180205; 6372; 6377; 6380; 6410; 6421; 6425; 6431; 6433; 6623; 6624; 6626; 6633; 6636; 6637; 6638; 6854; 6855; 6857; 6861; 6877; 6878; 6879; 7407; 7408; 7419; 7421; 7504; 7509; 7517; 7525; 7526; 7533; 7545; 7546; 7557; 7558; 7562; 7756; 7757; 7758; 7759; 7765; 7769; 7770; 7771; 7773; 7774; 7776; 7777; 7805; 7815; 7818; 7824; 7839; 7841; 7855; 7858; 7878; 7879; 8531; 8560; 8561; 8565; 8569; 8589; 8650; 8660; 8805; 8811; 8815; 8824; 8828; 8837; 8838; 8839; 8840; 8841; 8842; 8847; 8856; 8911; Attenuation coefficient; Bay of Plenty; Bottle, Niskin; Bounty Trough; Calculated after Maritorena and Morel, 2001; Campbell Plateau Physical Oceanography; Cast number; Chatham Rise; Chlorophyll a; Cruise/expedition; CTD, Sea-Bird, SBE 911plus; CTD, Seabird 19plus; CTD, SEA-BIRD SBE 9 plus; CTD/Rosette; CTD-RO; Date/Time of event; DEPTH, water; Depth of the euphotic zone; Elevation of event; Estimated; Event label; Filtration; Fluorescence; KAH1303; KAH1303_U7756; KAH1303_U7757; KAH1303_U7758; KAH1303_U7759; KAH1303_U7765; KAH1303_U7769; KAH1303_U7770; KAH1303_U7771; KAH1303_U7773; KAH1303_U7774; KAH1303_U7776; KAH1303_U7777; Kaharoa; Latitude of event; Longitude of event; Mixed layer depth; mixed-layer depth; New Zealand EEZ; New Zealand northeast shelf-slope; NIS; Nitrate; nutrients; Ocean and sea region; Oxygen; Phosphorus, reactive; Phytoplankton; Project; Salinity; Sample ID; Sample method; Sampling date; Silicate, reactive; Site; Size-fractionated chl a; SOAP (Surface Ocean Aerosol Production); Southwest Pacific; Spring Bloom II; TAN0902; TAN0902_U5806; TAN0902_U5809; TAN0902_U5819; TAN0902_U5829; TAN0902_U5833; TAN0909; TAN0909_U6372; TAN0909_U6377; TAN0909_U6380; TAN0909_U6410; TAN0909_U6421; TAN0909_U6425; TAN0909_U6431; TAN0909_U6433; TAN1006; TAN1006_U6623; TAN1006_U6624; TAN1006_U6626; TAN1006_U6633; TAN1006_U6636; TAN1006_U6637; TAN1006_U6638; TAN1103; TAN1103_U6854; TAN1103_U6855; TAN1103_U6857; TAN1103_U6861; TAN1103_U6877; TAN1103_U6878; TAN1103_U6879; TAN1113; TAN1113_U7407; TAN1113_U7408; TAN1113_U7419; TAN1113_U7421; TAN1203; TAN1204; TAN1204_U7545; TAN1204_U7546; TAN1204_U7557; TAN1204_U7558; TAN1204_U7562; TAN1212; TAN1212_SIS1; TAN1212_SIS2; TAN1212_SIS3; TAN1212_SIS4; TAN1212_SIS5; TAN1212_SIS6; TAN1212_SIS7; TAN1212_U7805; TAN1212_U7815; TAN1212_U7818; TAN1212_U7824; TAN1212_U7839; TAN1212_U7841; TAN1212_U7855; TAN1212_U7858; TAN1212_U7878; TAN1212_U7879; TAN1516; TAN1516_C10; TAN1516_C4; TAN1516_C6; TAN1516_C7; TAN1516_C8; TAN1516_C9; TAN1516_F1; TAN1516_F2; TAN1516_F3; TAN1516_S10; TAN1516_S15; TAN1516_S18; TAN1516_S22; TAN1516_S5; TAN1516_S9; TAN1604; TAN1604_U8531; TAN1604_U8560; TAN1604_U8561; TAN1604_U8565; TAN1604_U8569; TAN1604_U8589; TAN1604_U8650; TAN1604_U8660; TAN1702; TAN1702_10; TAN1702_11-2; TAN1702_17Jo; TAN1702_20; TAN1702_31; TAN1702_34; TAN1702_40; TAN1702_44; TAN1702_56; TAN1702_62; TAN1702_7; TAN1702_8; TAN1702_9; TAN1802_U8911; TAN1802, TAN1802_CTD; Tangaroa; Temperature, water; Temperature, water, potential; Transmissivity; U7504; U7505; U7508; U7509; U7517; U7518; U7525; U7526; U7533; Water mass
    Type: Dataset
    Format: text/tab-separated-values, 11227 data points
    Location Call Number Limitation Availability
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