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Chelsea Technologies Group Ltd fastpro8 software
Fastpro8 Software, supplied by Chelsea Technologies Group Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fastpro8+software/fastpro+software/10__1002_slash_lno__12716-79-10-12
Average 90 stars, based on 1 article reviews
fastpro8 software - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

Fluorescence:

Article Title: Plankton metabolic balance in the eastern Beagle Channel during spring
Article Snippet: Microbial community metabolic balance (i.e., the ratio between photosynthesis and community respiration) is critical for assessing the strength of the biological carbon pump and its importance for the marine food web.. This study aimed at characterizing the microbial community metabolic balance (hereinafter referred to as metabolic balance) in the Beagle Channel (BC, 54S, 68 W), a sub-Antarctic environment that connects the Pacific and Atlantic Oceans at the southernmost extreme of South America.. During a binational Chilean-Argentinian cruise along the eastern BC in the austral spring (November 2019), oxygen production and consumption rates were estimated in vitro after 12-h light and dark incubations.

Article Title: Dynamic variability of the phytoplankton electron requirement for carbon fixation in eastern Australian waters
Article Snippet: .. The biophysical model of Kolber et al. (1998) was fitted to all fluorescent transients using FastPro8 software (V.1.0.55; Chelsea Technologies) to determine minimum (F0, F′) and maximum fluorescence (Fm, Fm′), functional absorption cross section of PSII (σPSII, σPSII′) and the PSII connectivity factor (ρ, ρ′) (where the prime notation denotes that samples were measured during exposure to actinic light). ..

Article Title: Manganese co-limitation of phytoplankton growth and major nutrient drawdown in the Southern Ocean
Article Snippet: Chlorophyll-a concentrations were determined on glass fiber filters that were extracted in 90% acetone using a calibrated Turner Designs Trilogy fluorometer. .. Flow cytometry samples (2 mL) were preserved with paraformaldehyde (1% final concentration) and stored at –80 °C prior to analysis in the home laboratory on a FACSCalibur flow cytometer with CellQuest version 3.3 software (Becton Dickenson, Oxford, United Kingdom) following methods described in ref. . A FASTOcean Fast Repetition Rate fluorometer (Chelsea Technologies Group) was used to determine F v / F m . Fluorescence transients were fit in FASTPro8 software (Chelsea Technologies Group) to yield minimum fluorescence ( F o ) and maximum fluorescence ( F m ). .. Blank fluorescence of 0.2 μm sample filtrates was subtracted from F o and F m before calculation of F v / F m = ( F m – F o )/ F m . Nutrient samples for all experiments apart from Experiment 8 were analyzed on ship using a nutrient autoanalyzer (AA3, Seal Analytical).

Article Title: Different elemental stoichiometries of Fe‐limited <scp><i>Trichodesmium</i></scp> when grown under inorganic and organic phosphorus sources
Article Snippet: .. Recovery of minimum fluorescence (F0) and maximum fluorescence (Fm) using FASTPro8 software (Chelsea Technologies Group) allowed determination of the potential photochemical efficiency of photosystem II (PSII; Fv/Fm = (Fm Fo)/Fm). ..

Article Title: Thermal Performance Curves of Functional Traits Aid Understanding of Thermally Induced Changes in Diatom-Mediated Biogeochemical Fluxes
Article Snippet: A Chelsea Technologies FASTocean fluorometer supplied single-turnover excitation flashlets (of 1.1 μs duration) at 450 nm at a rate of 2 μs to achieve full saturation of PSII reaction centers followed by longer intervals of 100 μs to allow relaxation and re-oxidation of QA. .. Profiles of the fluorescence emission were fitted within the FastPro8 software (v. 1.0.55; Chelsea Technologies) to the Kolber-Prasil-Falkowski model to yield the minimum (FO or F ′; “indicates light adapted samples”) and maximum fluorescence (FM or F ′ M), effective absorption cross section of PSII (σ or σ′; nm2) and re-oxidation kinetic of QA (τ; μs). ..

Software:

Article Title: Plankton metabolic balance in the eastern Beagle Channel during spring
Article Snippet: Microbial community metabolic balance (i.e., the ratio between photosynthesis and community respiration) is critical for assessing the strength of the biological carbon pump and its importance for the marine food web.. This study aimed at characterizing the microbial community metabolic balance (hereinafter referred to as metabolic balance) in the Beagle Channel (BC, 54S, 68 W), a sub-Antarctic environment that connects the Pacific and Atlantic Oceans at the southernmost extreme of South America.. During a binational Chilean-Argentinian cruise along the eastern BC in the austral spring (November 2019), oxygen production and consumption rates were estimated in vitro after 12-h light and dark incubations.

Article Title: Phytoplankton physiology and functional traits under artificial upwelling with varying Si:N
Article Snippet: .. FastPro8 software (Chelsea Technologies) was used to process the data using the biophysical model of (Kolber et al., 1998). ..

Article Title: Dynamic variability of the phytoplankton electron requirement for carbon fixation in eastern Australian waters
Article Snippet: .. The biophysical model of Kolber et al. (1998) was fitted to all fluorescent transients using FastPro8 software (V.1.0.55; Chelsea Technologies) to determine minimum (F0, F′) and maximum fluorescence (Fm, Fm′), functional absorption cross section of PSII (σPSII, σPSII′) and the PSII connectivity factor (ρ, ρ′) (where the prime notation denotes that samples were measured during exposure to actinic light). ..

Article Title: Manganese co-limitation of phytoplankton growth and major nutrient drawdown in the Southern Ocean
Article Snippet: Chlorophyll-a concentrations were determined on glass fiber filters that were extracted in 90% acetone using a calibrated Turner Designs Trilogy fluorometer. .. Flow cytometry samples (2 mL) were preserved with paraformaldehyde (1% final concentration) and stored at –80 °C prior to analysis in the home laboratory on a FACSCalibur flow cytometer with CellQuest version 3.3 software (Becton Dickenson, Oxford, United Kingdom) following methods described in ref. . A FASTOcean Fast Repetition Rate fluorometer (Chelsea Technologies Group) was used to determine F v / F m . Fluorescence transients were fit in FASTPro8 software (Chelsea Technologies Group) to yield minimum fluorescence ( F o ) and maximum fluorescence ( F m ). .. Blank fluorescence of 0.2 μm sample filtrates was subtracted from F o and F m before calculation of F v / F m = ( F m – F o )/ F m . Nutrient samples for all experiments apart from Experiment 8 were analyzed on ship using a nutrient autoanalyzer (AA3, Seal Analytical).

Article Title: Different elemental stoichiometries of Fe‐limited <scp><i>Trichodesmium</i></scp> when grown under inorganic and organic phosphorus sources
Article Snippet: .. Recovery of minimum fluorescence (F0) and maximum fluorescence (Fm) using FASTPro8 software (Chelsea Technologies Group) allowed determination of the potential photochemical efficiency of photosystem II (PSII; Fv/Fm = (Fm Fo)/Fm). ..

Article Title: Thermal Performance Curves of Functional Traits Aid Understanding of Thermally Induced Changes in Diatom-Mediated Biogeochemical Fluxes
Article Snippet: A Chelsea Technologies FASTocean fluorometer supplied single-turnover excitation flashlets (of 1.1 μs duration) at 450 nm at a rate of 2 μs to achieve full saturation of PSII reaction centers followed by longer intervals of 100 μs to allow relaxation and re-oxidation of QA. .. Profiles of the fluorescence emission were fitted within the FastPro8 software (v. 1.0.55; Chelsea Technologies) to the Kolber-Prasil-Falkowski model to yield the minimum (FO or F ′; “indicates light adapted samples”) and maximum fluorescence (FM or F ′ M), effective absorption cross section of PSII (σ or σ′; nm2) and re-oxidation kinetic of QA (τ; μs). ..

Functional Assay:

Article Title: Dynamic variability of the phytoplankton electron requirement for carbon fixation in eastern Australian waters
Article Snippet: .. The biophysical model of Kolber et al. (1998) was fitted to all fluorescent transients using FastPro8 software (V.1.0.55; Chelsea Technologies) to determine minimum (F0, F′) and maximum fluorescence (Fm, Fm′), functional absorption cross section of PSII (σPSII, σPSII′) and the PSII connectivity factor (ρ, ρ′) (where the prime notation denotes that samples were measured during exposure to actinic light). ..

Flow Cytometry:

Article Title: Manganese co-limitation of phytoplankton growth and major nutrient drawdown in the Southern Ocean
Article Snippet: Chlorophyll-a concentrations were determined on glass fiber filters that were extracted in 90% acetone using a calibrated Turner Designs Trilogy fluorometer. .. Flow cytometry samples (2 mL) were preserved with paraformaldehyde (1% final concentration) and stored at –80 °C prior to analysis in the home laboratory on a FACSCalibur flow cytometer with CellQuest version 3.3 software (Becton Dickenson, Oxford, United Kingdom) following methods described in ref. . A FASTOcean Fast Repetition Rate fluorometer (Chelsea Technologies Group) was used to determine F v / F m . Fluorescence transients were fit in FASTPro8 software (Chelsea Technologies Group) to yield minimum fluorescence ( F o ) and maximum fluorescence ( F m ). .. Blank fluorescence of 0.2 μm sample filtrates was subtracted from F o and F m before calculation of F v / F m = ( F m – F o )/ F m . Nutrient samples for all experiments apart from Experiment 8 were analyzed on ship using a nutrient autoanalyzer (AA3, Seal Analytical).

Concentration Assay:

Article Title: Manganese co-limitation of phytoplankton growth and major nutrient drawdown in the Southern Ocean
Article Snippet: Chlorophyll-a concentrations were determined on glass fiber filters that were extracted in 90% acetone using a calibrated Turner Designs Trilogy fluorometer. .. Flow cytometry samples (2 mL) were preserved with paraformaldehyde (1% final concentration) and stored at –80 °C prior to analysis in the home laboratory on a FACSCalibur flow cytometer with CellQuest version 3.3 software (Becton Dickenson, Oxford, United Kingdom) following methods described in ref. . A FASTOcean Fast Repetition Rate fluorometer (Chelsea Technologies Group) was used to determine F v / F m . Fluorescence transients were fit in FASTPro8 software (Chelsea Technologies Group) to yield minimum fluorescence ( F o ) and maximum fluorescence ( F m ). .. Blank fluorescence of 0.2 μm sample filtrates was subtracted from F o and F m before calculation of F v / F m = ( F m – F o )/ F m . Nutrient samples for all experiments apart from Experiment 8 were analyzed on ship using a nutrient autoanalyzer (AA3, Seal Analytical).

other:

Article Title: Electron & Biomass Dynamics of Cyanothece Under Interacting Nitrogen & Carbon Limitations
Article Snippet: All fluorescence yields were adjusted for baseline fluorescence retrieved from parallel FRRf measurements upon filtrates of each sample passed through a 0.22 μm pore filter (cellulose acetate, syringe filter; Whatman, USA).



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