Overview
- Applications
-
- Algae cultivation
- Phytoplankton culture
- Microalgae research
- Synonyms
-
- {'name': '8_ppt_f_2_medium', 'source': 'unknown', 'original_category': 'algae'}
Composition
flowchart LR
CultureMech_000170["f_2_medium"]
ing0_1["1"]
CultureMech_000170 --> ing0_1
ing1_2["2"]
CultureMech_000170 --> ing1_2
ing2_3["3"]
CultureMech_000170 --> ing2_3
ing3_4["4"]
CultureMech_000170 --> ing3_4
ing4_5["5"]
CultureMech_000170 --> ing4_5
ing5_6["6"]
CultureMech_000170 --> ing5_6
ing6_7["7"]
CultureMech_000170 --> ing6_7
Ingredients (7)
| # | Ingredient | Concentration | Ontology | Notes |
|---|---|---|---|---|
| 1 | 1 | variable G_PER_L | Original amount: NaNO3(Fisher BP360-500) | |
| 2 | 2 | variable G_PER_L | Original amount: NaH2PO4•H2O(MCIB 742) | |
| 3 | 3 | variable G_PER_L | Original amount: Na2SiO3•9H2O(Sigma 307815) | |
| 4 | 4 | variable G_PER_L | Original amount: Trace Metals Solution | |
| 5 | 5 | variable G_PER_L | Original amount: Vitamin B12 | |
| 6 | 6 | variable G_PER_L | Original amount: Biotin Vitamin Solution | |
| 7 | 7 | variable G_PER_L | Original amount: Thiamine Vitamin Solution |
Preparation
- Important Notes To Consider: The quality of water, including natural seawater, is important.
- The term 'dH2O' generally refers to distilled, deionized, distilled/deionized water, Milli-Q water (Millipore Corp.), etc.
- Natural seawater and natural freshwater should be obtained from a non-polluted source. When dissolving chemicals, wait for the first component to dissolve before adding the second.
- Stirring, and sometimes the addition of heat, is often required to dissolve the chemicals efficiently.
- Preparation of stock solutions for frequently made algal culture media make preparing media convenient but also necessary to avoid errors from weighing very tiny amounts. Attention should be given to the pH of the final medium.
- In most cases, if pH adjustment is required, this occurs before sterilization.
- Please note that autoclaving removes carbon dioxide from media lacking carbonate stabilizing buffers.
- This would make the medium very alkaline soon after removal from the autoclave.
- In these cases, you should wait approximately 24 hours for gaseous equilibrium before inoculating the medium.
Target organisms and growth evidence
These are curated observations and conditions for named organisms; they do not imply universal growth suitability.
- Preferred term
- Tetraselmis marina
- Term
- Id
- NCBITaxon:41888
- Label
- Tetraselmis marina
- Growth metrics
- Measurement conditions
- F/2-medium for seven days in the first stage.
- Evidence
- Reference
- PMID:28456040
- Supports
- SUPPORT
- Snippet
- When the cells were grown in F/2-medium for seven days in the first stage, the carotenoid and lipid contents, and productivity were 44g/kg (DW), 27% and 31mg/L/d, respectively.
- Explanation
- Literature evidence states that Tetraselmis marina cells were grown in F/2 medium for seven days.
- Is max attainment
- False
- Measurement conditions
- F/2 first stage followed by three-day N-replete second stage with 4.41 mM NaNO3.
- Evidence
- Reference
- PMID:28456040
- Supports
- SUPPORT
- Snippet
- After second stage of cultivation of T. marina for further 3-days under N-replete condition (4.41mM NaNO3) increased biomass concentration of 1900mg/L and lipid content of 50% were observed
- Explanation
- Literature evidence reports increased biomass after an F/2-derived nitrogen-replete second-stage variant.
- Is max attainment
- False
- Preferred term
- Phaeodactylum tricornutum
- Term
- Id
- NCBITaxon:556484
- Label
- Phaeodactylum tricornutum CCAP 1055/1
- Strain
- UTEX 642
- Growth metrics
- Measurement conditions
- F/2ASW at 20 deg C, continuous illumination of 30-75 umol photons m-2 s-1, and aeration with ambient air or 1% CO2; reported mid-log harvest OD730 0.2-0.3.
- Evidence
- Reference
- DOI:10.1104/pp.18.00453
- Supports
- SUPPORT
- Explanation
- Matsui et al. explicitly report Phaeodactylum tricornutum UTEX 642 cultivation in F/2ASW.
- Is max attainment
- False
- Evidence
- Reference
- DOI:10.1104/pp.18.00453
- Supports
- SUPPORT
- Explanation
- The publication supports the organism-medium relationship for the F/2ASW variant of this parent F/2 medium record.
- Preferred term
- Thalassiosira pseudonana
- Term
- Id
- NCBITaxon:296543
- Label
- Thalassiosira pseudonana CCMP1335
- Strain
- CCMP1335
- Growth metrics
- Measurement conditions
- F/2ASW at 20 deg C, continuous illumination of 30-75 umol photons m-2 s-1, and aeration with ambient air or 1% CO2; reported mid-log harvest OD730 0.1-0.15.
- Evidence
- Reference
- DOI:10.1104/pp.18.00453
- Supports
- SUPPORT
- Explanation
- Matsui et al. explicitly report Thalassiosira pseudonana CCMP1335 cultivation in F/2ASW.
- Is max attainment
- False
- Evidence
- Reference
- DOI:10.1104/pp.18.00453
- Supports
- SUPPORT
- Explanation
- The source supports growth on the F/2ASW variant for the same strain represented by NCBI Taxonomy ID 296543 and reference assembly GCF_000149405.2.
- Preferred term
- Chaetoceros gracilis
- Strain
- UTEX LB2658
- Growth metrics
- Measurement conditions
- Modified F/2ASW supplemented with sodium selenite and sodium metasilicate; sodium concentration adjusted by NaCl addition and CO2 availability varied.
- Evidence
- Reference
- DOI:10.1007/s10126-021-10037-4
- Supports
- SUPPORT
- Explanation
- Tsuji et al. report growth and CO2-concentrating mechanism experiments for Chaetoceros gracilis UTEX LB2658 using modified F/2ASW.
- Is max attainment
- False
- Evidence
- Reference
- DOI:10.1007/s10126-021-10037-4
- Supports
- SUPPORT
- Explanation
- The study identifies the UTEX LB2658 strain and modified F/2ASW growth conditions; the UTEX strain page separately lists this strain as a liquid-culture Chaetoceros gracilis accession.
Recipe variants
- Name
- n_replete_second_stage_tetraselmis_marina
- Description
- F/2 culture followed by nitrogen-replete second-stage cultivation for enhanced biomass and lipid productivity of Tetraselmis marina.
- Modifications
- Grow cells in F/2 medium for seven days as the first stage.
- Shift to a nitrogen-replete second stage with 4.41 mM NaNO3 for three days.
- Purpose
- Capture a study-specific F/2-derived nitrogen repletion variant used to increase Tetraselmis marina biomass and lipid productivity.
- Evidence
- Reference
- PMID:28456040
- Supports
- SUPPORT
- Snippet
- After second stage of cultivation of T. marina for further 3-days under N-replete condition (4.41mM NaNO3) increased biomass concentration of 1900mg/L and lipid content of 50% were observed
- Explanation
- Literature evidence describes a nitrogen-replete second-stage variant after initial F/2 cultivation.
- Name
- f_2asw_diatom_culture
- Description
- F/2 artificial seawater culture conditions used for marine diatom maintenance and transformation studies.
- Modifications
- Use artificial seawater supplemented with half-strength Guillard f solution.
- Maintain cultures at 20 deg C under continuous illumination at 30-75 umol photons m-2 s-1.
- Aerate cultures with ambient air or 1% CO2 depending on the experiment.
- Purpose
- Represent F/2ASW as a study-specific F/2 medium implementation for marine diatoms.
- Evidence
- Reference
- DOI:10.1104/pp.18.00453
- Supports
- SUPPORT
- Explanation
- Matsui et al. define F/2ASW as artificial seawater plus half-strength Guillard f solution and report use with Phaeodactylum tricornutum UTEX 642 and Thalassiosira pseudonana CCMP1335.
- Name
- modified_f_2asw_sodium_response
- Description
- Modified F/2 artificial seawater used for sodium and CO2 response experiments with Chaetoceros gracilis.
- Modifications
- Supplement F/2ASW with 10 nM sodium selenite and 0.1 mM sodium metasilicate.
- Adjust sodium concentration by altering NaCl addition to the basal medium.
- Vary CO2 availability to distinguish sodium-dependent growth effects.
- Purpose
- Capture an experimental F/2ASW variant used to study carbon concentrating mechanism physiology.
- Evidence
- Reference
- DOI:10.1007/s10126-021-10037-4
- Supports
- SUPPORT
- Explanation
- Tsuji et al. report Chaetoceros gracilis UTEX LB2658 growth experiments using a modified F/2ASW formulation.
Provenance
Merged from 2 source records.
- 8_ppt_F_2_Medium (CultureMech:000021)
- F_2_Medium (CultureMech:000170)
| Timestamp | Curator | Action | Notes |
|---|---|---|---|
| 2026-01-28 | utex-import | Imported from UTEX Culture Collection | Source ID: f-2-medium, URL: https://utex.org/products/f-2-medium |
| 2026-03-13T06:18:53.395564Z | culturemech-id-assigner-v1.0 | Assigned CultureMech ID | Assigned stable identifier: CultureMech:000170 |
| 2026-03-17T19:45:04.333217+00:00 | normalize_media_names_to_snake_case.py | NAME_NORMALIZED | Normalized name from "F/2 Medium" to "f_2_medium" for consistent matching |
| 2026-05-09T14:15:00-07:00 | culturemech-agentic-curation | ADDED_GROWTH_EVIDENCE | Added strain-specific F/2ASW and modified F/2ASW growth evidence from Falcon report review and primary literature metadata. |
| 2026-08-06T00:58:02.514496+00:00 | curate_organism_culture_type.py | SET_ORGANISM_CULTURE_TYPE | Inferred isolate: 4 specific strain(s) named, no community signal (#142) |
| 2026-08-06T03:04:19.327570+00:00 | recipe-merger | Merged 2 duplicate recipes into canonical record | Sources: 8_ppt_F_2_Medium, F_2_Medium |
| 2026-08-06T03:04:19.327609+00:00 | merge_recipes.py | MERGED_RECIPES | merged 2 source recipe(s) on fingerprint 8dae5bfc930f029e490887cee3f3f23255184001b3487f4c426b3193452a56c5 |