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Rehder, Linda; Rost, Björn; Rokitta, Sebastian D (2023): Temperature effects on the physiology of photosynthesis and respiration in Phaeodactylum tricornutum [dataset]. PANGAEA, https://doi.org/10.1594/PANGAEA.960034

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Abstract:
Phaeodactylum tricornutum strain CCAP 1052/1A was cultivated at 6°C and 15°C under controlled conditions (32 salinity, F/2 medium, 400 µatm pCO2, 100 µmol photons m-2 s-2 light intentsity 16:8 light:dark cycle) in semi-continous batch cultures. We assessed the carbonate chemistry (pH, total alkalinity, dissolved inorganic carbon), growth rates, particulate organic carbon and nitrogen (POC and PON), chlorophyll a quota (Chl a), POC:PON ratios, Chl a:POC ratios as well as production rates at both acclimation temperatures. Additionally, we performed biological invivo assays to measure rates of gross photosynthetic oxygen release, gross photosynthetic carbon uptake, respiratory oxygen uptake and respiratory carbon release using membrane-inlet mass-spectrometry. Assays were performed in photosynthesis-irradiance-(PI-)curves of increasing light intensity (0, 50, 150, 250, 400 µmol photons m-2 s-2). First rates were measured under acclimation temperature (6°C and 15°C), directly afterwards, the assay temperature was abruptly shifted to 15°C or 6°C, respectively, and the PI-curve measurement was repeated, so that 6°C acclimated cells were measured at 15°C and 15°C acclimated cells were measured at 6°C. Q10 factors were calculated from acclimated cells und the respective temperature shift. Photosynthetic and respiratory quotients were calculated for acclimated cells as well as after the abrupt temperature shift. PI-parameters, i.e. maximum photosynthesis rate, light use efficiency and light saturation index were calculated. All experiments were performed in laboratories at the Alfred-Wegener-Institute Bremerhaven.
Keyword(s):
Diatom; Laboratory experiment; Phaeodactylum tricornutum; Photosynthesis; Physiological performance; Phytoplankton; Respiration; Temperature
Supplement to:
Rehder, Linda; Rost, Björn; Rokitta, Sebastian D (2023): Abrupt and acclimation responses to changing temperature elicit divergent physiological effects in the diatom Phaeodactylum tricornutum. New Phytologist, 239(3), 1005-1013, https://doi.org/10.1111/nph.18982
References:
Guillard, R R L; Ryther, J H (1962): Studies of marine planktonic diatoms. I. Cyclotella nana Hustedt, and Detonula confervacea (cleve) Gran. Canadian Journal of Microbiology, 8(2), 229-239, https://doi.org/10.1139/m62-029
Knap, Anthony H; Michaels, A; Close, A R; Ducklow, Hugh W; Dickson, Andrew G (1996): Protocols for the Joint Global Ocean Flux Study (JGOFS) Core Measurements. JGOFS, Reprint of the IOC Manuals and Guides No. 29, UNESCO 1994, 19, 210 pp, hdl:10013/epic.27912.d001
Rokitta, Sebastian D; Rost, Björn (2012): Effects of CO2 and their modulation by light in the life-cycle stages of the coccolithophore Emiliania huxleyi. Limnology and Oceanography, 57(2), 607-618, https://doi.org/10.4319/lo.2012.57.2.0607
Additional metadata:
Rehder, Linda (2023): Detailed parameter information for Phaeodactylum tricornutum data. Pangaea_Parameter_Rehder_et_al.csv
Comment:
Phaeodactylum tricornutum strain CCAP 1052/1A was originally sampled in 2003 from an estuary, polluted water (industrial area and seaside resort) Blackpool, England (detailed information from Culture Collection of algae and protozoa; https://www.ccap.ac.uk/catalogue/strain-1055-1). Prior to the experiments, the culture was at least one year cultivated at 15°C in North Sea water enriched with F/2 medium under 16:8 light:dark irradiance of ~10 µmol photons m-2 s-1 with regular dilution every ~4 weeks.
Experiment 1A and 1B refer to 'bulk' parameter measurements, i.e. growth rates, biomass and pigmentation. Due to logistical issues, Exp_1A and Exp_1B are from different batches, but the same stock culture. Exp_2 is the same batch as Exp_1A and refers to physiological measurements. Temperature shifts only apply to Exp_2 and took place after cultures were concentrated and physiological rates were measured under in-situ temperature at four different light levels in the membrane inlet mass spectrometer (MIMS). The temperature shift took place inside the cuvette of the MIMS and took ~1 h.
Parameter(s):
#NameShort NameUnitPrincipal InvestigatorMethod/DeviceComment
1ExperimentExpRehder, Linda
2Date/time start, experimentDate/time start expRehder, Lindaincluding acclimation time for Exp_1A
3Date/time end, experimentDate/time end expRehder, Linda
4Sampling date/time, experimentDate/time sampling expRehder, Linda
5Sample IDSample IDRehder, Linda
6Type of studyStudy typeRehder, Linda
7LaboratoryLabRehder, Linda
8SpeciesSpeciesRehder, Linda
9Species, unique identificationSpecies UIDRehder, Linda
10Species, unique identification (Semantic URI)Species UID (Semantic URI)Rehder, Linda
11Species, unique identification (URI)Species UID (URI)Rehder, Linda
12StrainStrainRehder, Linda
13Treatment: temperatureT:temp°CRehder, Linda
14Treatment: light:dark cycleT:L:Dhh:hhRehder, Linda
15Treatment: light intensityT:Ioµmol/m2/sRehder, Linda
16SalinitySalRehder, Linda
17MediumMediumRehder, Linda
18GenerationGeneration#Rehder, Lindain acclimation
19pHpHRehder, LindaNBS scale
20Alkalinity, totalATµmol/kgRehder, LindaTitration analyzer, Schott Instruments, TitroLine alpha plus
21Carbon, inorganic, dissolvedDICµmol/kgRehder, LindaMeasured with colorimetric assay on QuAAtro continuous segmented flow analyzer (Seal Analytical)
22Growth rateµ1/dayRehder, LindaCoulter Counter (Beckman Coulter)
23Carbon, organic, particulate, per cellPOC/cellpg/#Rehder, LindaElemental analyzer, EuroVector, EA 3000
24Nitrogen, organic, particulate, per cellPON/cellpg/#Rehder, LindaElemental analyzer, EuroVector, EA 3000
25Carbon, organic, particulate/Nitrogen, organic, particulate ratioPOC/PONmol/molRehder, LindaCalculated
26Particulate organic carbon production per cellPOC prod/cellpg/#/dayRehder, LindaCalculatedµ*POC
27Chlorophyll a per cellChl a/cellpg/#Rehder, LindaLaboratory fluorometer, Turner, Trilogy
28Chlorophyll a/particulate organic carbon ratioChl a/POCRehder, LindaCalculatedpg/pg
29Respiratory oxygen uptake rate, per chlorophyll aRO2µmol/mg/hRehder, LindaMembrane inlet mass spectrometer (MIMS), GV Instruments, IsoprimeRO2_accl: rate of respiratory O2 uptake under acclimation temperature
30Respiratory oxygen uptake rate, per chlorophyll aRO2µmol/mg/hRehder, LindaMembrane inlet mass spectrometer (MIMS), GV Instruments, IsoprimeRO2_shifted: rate of respiratory O2 uptake after abrupt temperature shift
31Factor quantifying temperature dependent change of rates of processesQ10Rehder, LindaCalculation according to Rehder et al. (2023)Q10 of RO2, calculated from RO2_accl and RO2_shifted
32Respiratory carbon release rate, per chlorophyll aRCO2µmol/mg/hRehder, LindaMembrane inlet mass spectrometer (MIMS), GV Instruments, IsoprimeRCO2_accl: rate of respiratory CO2 release under acclimation temperature
33Respiratory carbon release rate, per chlorophyll aRCO2µmol/mg/hRehder, LindaMembrane inlet mass spectrometer (MIMS), GV Instruments, IsoprimeRCO2_shifted: rate of respiratory CO2 release after abrupt temperature shift
34Factor quantifying temperature dependent change of rates of processesQ10Rehder, LindaCalculation according to Rehder et al. (2023)Q10 of RO2, calculated from RO2_accl and RO2_shifted
35Respiratory quotientRQRehder, LindaCalculation according to Rehder et al. (2023)after acclimation
36Respiratory quotientRQRehder, LindaCalculation according to Rehder et al. (2023)after the abrupt temperature shift
37Gross photosynthetic oxygen release rate, per chlorophyll aPSO2µmol/mg/hRehder, LindaMembrane inlet mass spectrometer (MIMS), GV Instruments, IsoprimePSO2_accl_V150: rate of photosynthetic O2 release under acclimation temperature at in-situ light intensity
38Gross photosynthetic oxygen release rate, per chlorophyll aPSO2µmol/mg/hRehder, LindaMembrane inlet mass spectrometer (MIMS), GV Instruments, IsoprimePSO2_shifted_V150: rate of photosynthetic O2 release after abrupt temperature shift at in-situ light intensity
39Factor quantifying temperature dependent change of rates of processesQ10Rehder, LindaCalculation according to Rehder et al. (2023)Q10 of PSO2 at in-situ light intensity, calculated from PSO2_accl_V150 and PSO2_shifted_V150
40Gross photosynthetic carbon uptake rate, per chlorophyll aPSCO2µmol/mg/hRehder, LindaMembrane inlet mass spectrometer (MIMS), GV Instruments, IsoprimePSCO2_accl_V150: rate of photosynthetic C uptake under acclimation temperature at in-situ light intensity
41Gross photosynthetic carbon uptake rate, per chlorophyll aPSCO2µmol/mg/hRehder, LindaMembrane inlet mass spectrometer (MIMS), GV Instruments, IsoprimePSCO2_shifted_V150: rate of photosynthetic C uptake after abrupt temperature shift at in-situ light intensity
42Factor quantifying temperature dependent change of rates of processesQ10Rehder, LindaCalculation according to Rehder et al. (2023)Q10 of PSO2 at in-situ light intensity, calculated from PSO2_accl_V150 and PSO2_shifted_V150
43Photosynthetic quotientPQRehder, LindaCalculation according to Rehder et al. (2023)under acclimation temperature at in-situ light intensity
44Photosynthetic quotientPQRehder, LindaCalculation according to Rehder et al. (2023)after abrupt temperature shift at in-situ light intensity
45Maximum photosynthetic oxygen release rate, per chlorophyll aPSO2 Vmaxµmol/mg/hRehder, LindaMembrane inlet mass spectrometer (MIMS), GV Instruments, IsoprimePSO2_accl_Vmax: maximum rate of photosynthetic O2 release under acclimation temperature
46Maximum photosynthetic oxygen release rate, per chlorophyll aPSO2 Vmaxµmol/mg/hRehder, LindaMembrane inlet mass spectrometer (MIMS), GV Instruments, IsoprimePSO2_shifted_Vmax: maximum rate of photosynthetic O2 releaseafter abrupt temperature shift
47Factor quantifying temperature dependent change of rates of processesQ10Rehder, LindaCalculation according to Rehder et al. (2023)Q10 of maximum PSO2, calculated PSO2_accl_Vmax and PSO2_shifted_Vmax
48Maximum photosynthetic carbon uptake rate, per chlorophyll aPSCO2 Vmaxµmol/mg/hRehder, LindaMembrane inlet mass spectrometer (MIMS), GV Instruments, IsoprimePSCO2_accl_Vmax: maximum rate of photosynthetic C uptake under acclimation temperature
49Maximum photosynthetic carbon uptake rate, per chlorophyll aPSCO2 Vmaxµmol/mg/hRehder, LindaMembrane inlet mass spectrometer (MIMS), GV Instruments, IsoprimePSCO2_shifted_Vmax: maximum rate of photosynthetic C uptake after abrupt temperature shift
50Factor quantifying temperature dependent change of rates of processesQ10Rehder, LindaCalculation according to Rehder et al. (2023)Q10 of maximum PSCO2, calculated PSCO2_accl_Vmax and PSCO2_shifted_Vmax
51Light saturation indexIkµmol/m2/sRehder, LindaCalculation according to Rokitta & Rost (2012)Ik of PSO2 under acclimation temperature
52Light saturation indexIkµmol/m2/sRehder, LindaCalculation according to Rokitta & Rost (2012)Ik of PSO2 after abrupt temperature shift
53Light use efficiencyalphaµmol/m2/sRehder, LindaCalculation according to Rokitta & Rost (2012)alpha of PSO2 under acclimation temperature
54Light use efficiencyalphaµmol/m2/sRehder, LindaCalculation according to Rokitta & Rost (2012)alpha of PSO2 after abrupt temperature shift
55Light saturation indexIkµmol/m2/sRehder, LindaCalculation according to Rokitta & Rost (2012)Ik of PSCO2 under acclimation temperature
56Light saturation indexIkµmol/m2/sRehder, LindaCalculation according to Rokitta & Rost (2012)Ik of PSCO2 after abrupt temperature shift
57Light use efficiencyalphaµmol/m2/sRehder, LindaCalculation according to Rokitta & Rost (2012)alpha of PSCO2 under acclimation temperature
58Light use efficiencyalphaµmol/m2/sRehder, LindaCalculation according to Rokitta & Rost (2012)alpha of PSCO2 after abrupt temperature shift
Status:
Curation Level: Enhanced curation (CurationLevelC)
Size:
736 data points

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