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  • 1
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Regaudie-de-Gioux, Aurore; Huete-Ortega, Maria; Sobrino, Cristina; López-Sandoval, Daffne C; González, N; Fernández-Carrera, Ana; Vidal, Montserrat; Marañón, Emilio; Cermeño, Pedro; Latasa, Mikel; Agustí, Susana; Duarte, Carlos Manuel (2019): Multi-model remote sensing assessment of primary production in the subtropical gyres. Journal of Marine Systems, 196, 97-106, https://doi.org/10.1016/j.jmarsys.2019.03.007
    Publication Date: 2023-09-20
    Description: Seawater was sampled from five depths in the euphotic zone corresponding to 100 % (ca. 3 m depth), 50 %, 20 %, 7 % and 1 % of incident Photosynthetically Active Radiation (PAR). For each depth, four 72 mL polystyrene bottles (three clear bottles and one dark bottle) were filled with unfiltered seawater, inoculated with 10 - 20 µCi NaH¹⁴CO₃ and incubated on-deck from dawn to dusk. Temperature and irradiance in the incubators simulated the water temperature and the incident irradiance at the corresponding depth of each sample by using a combination of neutral density and blue filters (Mist Blue, ref. 061, Lee Filters ®). After incubation, samples from three of the five depths (100 %, 20 % and 1 % PAR) were sequentially filtered through 20, 2 and 0.2 µm polycarbonate filters while the other depths (50 % and 7 % PAR) were directly filtered by 0.2 µm. Immediately after filtering, filters were then exposed to concentrated HCl fumes at least 12 h to remove the non-fixed inorganic ¹⁴C. Filters were placed in scintillation vials to which 5 mL of liquid scintillation cocktail was added. The radioactivity on each filter (disintegrations per minute, DPM) was determined using a Wallac scintillation counter. To compute the rate of photosynthetic carbon fixation, the dark-bottle DPM was subtracted from the light-bottle DPM values. A constant value of 24,720 µg L-1 (or 2,060 µmol L-1) was assumed for the concentration of dissolved inorganic carbon for surface waters in tropical ocean (Key et al., 2004). A correction factor of 1.05 was applied to this constant value for discrimination isotopic. Total primary production was calculated as the sum of the primary production on each size class.
    Keywords: 29HE20101215; 29HE20110117; 29HE20110211; 29HE20110317; 29HE20110416; 29HE20110513; 29HE20110619; CSIC; CTD/Rosette; CTD-RO; Date/Time of event; DEPTH, water; Event label; Hespérides; Latitude of event; Longitude of event; MALASPINA_LEG1; MALASPINA_LEG1_006-3; MALASPINA_LEG1_007-3; MALASPINA_LEG1_008-3; MALASPINA_LEG1_009-3; MALASPINA_LEG1_010-3; MALASPINA_LEG1_011-3; MALASPINA_LEG1_012-3; MALASPINA_LEG1_013-3; MALASPINA_LEG1_014-3; MALASPINA_LEG1_015-3; MALASPINA_LEG1_016-3; MALASPINA_LEG1_017-3; MALASPINA_LEG1_018-3; MALASPINA_LEG1_019-3; MALASPINA_LEG1_020-3; MALASPINA_LEG1_022-3; MALASPINA_LEG1_023-3; MALASPINA_LEG1_024-3; MALASPINA_LEG1_025-3; MALASPINA_LEG1_026-3; MALASPINA_LEG2; MALASPINA_LEG2_027-3; MALASPINA_LEG2_028-3; MALASPINA_LEG2_029-3; MALASPINA_LEG2_030-3; MALASPINA_LEG2_031-3; MALASPINA_LEG2_032-3; MALASPINA_LEG2_033-3; MALASPINA_LEG2_034-3; MALASPINA_LEG2_035-3; MALASPINA_LEG2_037-3; MALASPINA_LEG2_038-3; MALASPINA_LEG2_040-3; MALASPINA_LEG2_041-3; MALASPINA_LEG2_042-3; MALASPINA_LEG2_043-3; MALASPINA_LEG2_044-3; MALASPINA_LEG3; MALASPINA_LEG3_046-3; MALASPINA_LEG3_047-3; MALASPINA_LEG3_048-3; MALASPINA_LEG3_049-3; MALASPINA_LEG3_050-3; MALASPINA_LEG3_051-3; MALASPINA_LEG3_052-3; MALASPINA_LEG3_053-3; MALASPINA_LEG3_054-3; MALASPINA_LEG3_055-3; MALASPINA_LEG3_056-3; MALASPINA_LEG3_057-3; MALASPINA_LEG3_058-3; MALASPINA_LEG3_059-3; MALASPINA_LEG3_060-3; MALASPINA_LEG3_061-3; MALASPINA_LEG3_062-3; MALASPINA_LEG3_063-3; MALASPINA_LEG3_064-3; MALASPINA_LEG3_065-3; MALASPINA_LEG3_066-3; MALASPINA_LEG3_068-3; MALASPINA_LEG4; MALASPINA_LEG4_069-3; MALASPINA_LEG4_070-3; MALASPINA_LEG4_071-3; MALASPINA_LEG4_072-3; MALASPINA_LEG4_073-3; MALASPINA_LEG4_074-3; MALASPINA_LEG4_075-3; MALASPINA_LEG4_076-3; MALASPINA_LEG5; MALASPINA_LEG5_083-3; MALASPINA_LEG5_084-3; MALASPINA_LEG5_085-3; MALASPINA_LEG5_086-3; MALASPINA_LEG5_087-3; MALASPINA_LEG5_088-3; MALASPINA_LEG5_089-3; MALASPINA_LEG5_090-3; MALASPINA_LEG5_091-3; MALASPINA_LEG5_092-3; MALASPINA_LEG5_093-3; MALASPINA_LEG5_094-3; MALASPINA_LEG5_095-3; MALASPINA_LEG5_096-3; MALASPINA_LEG5_097-3; MALASPINA_LEG5_098-3; MALASPINA_LEG5_099-3; MALASPINA_LEG6; MALASPINA_LEG6_104-3; MALASPINA_LEG6_106-3; MALASPINA_LEG6_107-3; MALASPINA_LEG6_108-3; MALASPINA_LEG6_109-3; MALASPINA_LEG6_110-3; MALASPINA_LEG6_111-3; MALASPINA_LEG6_113-3; MALASPINA_LEG6_114-3; MALASPINA_LEG6_115-3; MALASPINA_LEG6_117-3; MALASPINA_LEG6_118-3; MALASPINA_LEG6_119-3; MALASPINA_LEG6_120-3; MALASPINA_LEG6_121-3; MALASPINA_LEG6_122-3; MALASPINA_LEG6_123-3; MALASPINA_LEG6_124-3; MALASPINA_LEG6_125-3; MALASPINA_LEG6_126-3; MALASPINA_LEG7; MALASPINA_LEG7_127-3; MALASPINA_LEG7_128-3; MALASPINA_LEG7_129-3; MALASPINA_LEG7_130-3; MALASPINA_LEG7_131-3; MALASPINA_LEG7_132-3; MALASPINA_LEG7_133-3; MALASPINA_LEG7_134-3; MALASPINA_LEG7_135-3; MALASPINA_LEG7_136-3; MALASPINA_LEG7_137-3; MALASPINA_LEG7_138-3; MALASPINA_LEG7_139-3; MALASPINA_LEG7_140-3; MALASPINA_LEG7_141-3; MALASPINA_LEG7_142-3; MALASPINA_LEG7_143-3; MALASPINA_LEG7_144-3; MALASPINA_LEG7_145-3; MALASPINA_LEG7_146-3; MALASPINA_LEG7_147-3; MALASPINA-2010; Malaspina circumnavigation expedition; MH008_006; MH009_007; MH010_008; MH011_009; MH012_010; MH013_011; MH014_012; MH015_013; MH016_014; MH017_015; MH018_016; MH019_017; MH020_018; MH021_019; MH022_020; MH024_022; MH025_023; MH026_024; MH027_025; MH028_026; MH036_027; MH037_028; MH038_029; MH039_030; MH040_031; MH041_032; MH042_033; MH043_034; MH044_035; MH046_037; MH047_038; MH049_040; MH050_041; MH051_042; MH052_043; MH053_044; MH062_046; MH063_047; MH064_048; MH065_049; MH066_050; MH067_051; MH072_052; MH073_053; MH074_054; MH075_055; MH076_056; MH077_057; MH078_058; MH079_059; MH080_060; MH081_061; MH082_062; MH083_063; MH084_064; MH085_065; MH086_066; MH088_068; MH095_069; MH096_070; MH097_071; MH098_072; MH099_073; MH100_074; MH101_075; MH102_076; MH127_083; MH128_084; MH129_085; MH130_086; MH131_087; MH132_088; MH133_089; MH134_090; MH135_091; MH136_092; MH137_093; MH138_094; MH139_095; MH140_096; MH141_097; MH142_098; MH143_099; MH153_104; MH155_106; MH156_107; MH157_108; MH158_109; MH159_110; MH160_111; MH162_113; MH163_114; MH164_115; MH166_117; MH167_118; MH168_119; MH169_120; MH170_121; MH171_122; MH172_123; MH173_124; MH174_125; MH175_126; MH188_127; MH189_128; MH190_129; MH191_130; MH193_131; MH194_132; MH195_133; MH196_134; MH197_135; MH198_136; MH199_137; MH200_138; MH201_139; MH202_140; MH203_141; MH204_142; MH205_143; MH206_144; MH207_145; MH208_146; MH209_147; primary production; Primary production of carbon, standard deviation; Primary production of carbon per hour; see abstract; subtropical gyres
    Type: Dataset
    Format: text/tab-separated-values, 1241 data points
    Location Call Number Limitation Availability
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  • 2
    Publication Date: 2024-03-14
    Keywords: Calcium carbonate production of carbon; Calcium carbonate production of carbon, standard deviation; Coccolithophoridae, total; Cruise/expedition; DATE/TIME; DEPTH, water; Emiliania huxleyi; Incubation duration; LATITUDE; LONGITUDE; Method comment; Ocean and sea region; Percentage; Primary production of carbon; Primary production of carbon, standard deviation; Principal investigator; Reference/source; Station label; Uniform resource locator/link to reference
    Type: Dataset
    Format: text/tab-separated-values, 35037 data points
    Location Call Number Limitation Availability
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  • 3
    Publication Date: 2020-02-06
    Description: Upwelling is the process by which deep, cold, relatively high-CO2, nutrient-rich seawater rises to the sunlit surface of the ocean. This seasonal process has fueled geoengineering initiatives to fertilize the surface ocean with deep seawater to enhance productivity and thus promote the drawdown of CO2. Coccolithophores, which inhabit many upwelling regions naturally ‘fertilized’ by deep seawater, have been investigated in the laboratory in the context of ocean acidification to determine the extent to which nutrients and CO2 impact their physiology, but few data exist in the field except from mesocosms. Here, we used the Porcupine Abyssal Plain (north Atlantic Ocean) Observatory to retrieve seawater from depths with elevated CO2 and nutrients, mimicking geoengineering approaches. We tested the effects of abrupt natural deep seawater fertilization on the physiology and biogeochemistry of two strains of Emiliania huxleyi of known physiology. None of the strains tested underwent cell divisions when incubated in waters obtained from 〈1,000 m (pH = 7.99–8.08; CO2 = 373–485 p.p.m; 1.5–12 μM nitrate). However, growth was promoted in both strains when cells were incubated in seawater from ~1,000 m (pH = 7.9; CO2 ~560 p.p.m.; 14–17 μM nitrate) and ~4,800 m (pH = 7.9; CO2 ~600 p.p.m.; 21 μM nitrate). Emiliania huxleyi strain CCMP 88E showed no differences in growth rate or in cellular content or production rates of particulate organic (POC) and inorganic (PIC) carbon and cellular particulate organic nitrogen (PON) between treatments using water from 1,000 m and 4,800 m. However, despite the N:P ratio of seawater being comparable in water from ~1,000 and ~4,800 m, the PON production rates were three times lower in one incubation using water from ~1,000 m compared to values observed in water from ~4,800 m. Thus, the POC:PON ratios were threefold higher in cells that were incubated in ~1,000 m seawater. The heavily calcified strain NZEH exhibited lower growth rates and PIC production rates when incubated in water from ~4,800 m compared to ~1,000 m, while cellular PIC, POC and PON were higher in water from 4,800 m. Calcite Sr/Ca ratios increased with depth despite constant seawater Sr/Ca, indicating that upwelling changes coccolith geochemistry. Our study provides the first experimental and field trial of a geoengineering approach to test how deep seawater impacts coccolithophore physiological and biogeochemical properties. Given that coccolithophore growth was only stimulated using waters obtained from 〉1,000 m, artificial upwelling using shallower waters may not be a suitable approach for promoting carbon sequestration for some locations and assemblages, and should therefore be investigated on a site-by-site basis.
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
    Format: text
    Location Call Number Limitation Availability
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