References [ 9 ]
Thamatrakoln K & Hildebrand M (2008) Silicon uptake in diatoms revisited: A model for saturable and nonsaturable uptake kinetics and the role of silicon transporters. Plant Physiology 146: 1397-1407.
Hazelaar S, van der Strate HJ, Gieskes WWC & Vrieling EG (2003) Possible role of ubiquitin in silica biomineralization in diatoms: Identification of a homologue with high silica affinity. Biomolecular Engineering 20: 163-169.
Rampen SW, Schouten S, Panoto FE, Brink M, Andersen RA, Muyzer G, Abbas B & Sinninghe Damste JS (2009) Phylogenetic position of Attheya longicornis and Attheya septentrionalis (Bacillariophyta). Journal of Phycology 45: 444-453.
Jiang L, Eriksson J, Lage S, Jonasson S, Shams S, Mehine M, Ilag LL & Rasmussen U (2014) Diatoms: A novel source for the neurotixin BMAA in aquatic environments. PLoS ONE 9: e84578.
Slocombe SP, Zhang QY, Ross M, Anderson A, Thomas NJ, Lapresa A, Rad Menéndez C, Campbell CN, Black KD, Stanley MS & Day JG (2015) Unlocking nature's treasure-chest: Screening for oleaginous algae. Scientific Reports 5: 09844.
Guo J, Selby K & Boxall A (2016) Comparing the sensitivity of chlorophytes, cyanobacteria and diatoms to major-use antibiotics. Environmental Toxicology and Chemistry 35: 2587-2596.
Vannoni M, Creach V, Barry J & Sheahan D (2018) Chlorine toxicity to Navicula pelliculosa and Achnanthes spp. in a flow-through system: The use of immobilised microalgae and variable chlorophyll fluorescence Aquatic Toxicology 202: 80-89.
Clement R, Jensen E, Prioretti L, Maberly S & Gontero B (2017) Diversity of CO2-concentrating mechanisms and responses to CO2 concentration in marine and freshwater diatoms Journal of Experimental Botany 68: 3925-3935.
Lage S, Ström L, Godhe A & Rydberg S (2019) Kinetics of ß-N-methylamino-L-alanine (BMAA)) and 2, 4-diaminobutyric acid (DAB) production by diatoms: the effect of nitrogen European Journal of Phycology 54: 115-125.
Sequences [ 3 ]
EMBL/Genbank Links
(Bold text = submission by CCAP staff or collaborators)
18S
Division/Phylum: Heterokontophyta/Ochrophyta Class: Bacillariophyceae Order: Naviculales

Note: for strains where we have DNA barcodes we can be reasonably confident of identity, however for those not yet sequenced we rely on morphology and the original identification, usually made by the depositor. Although CCAP makes every effort to ensure the correct taxonomic identity of strains, we cannot guarantee that a strain is correctly identified at the species, genus or class levels. On this basis users are responsible for confirming the identity of the strain(s) they receive from us on arrival before starting experiments.
For strain taxonomy we generally use AlgaeBase for algae and Adl et al. (2019) for protists.

Culture media, purity and growth conditions:
Medium: f/2 + Si; Bacteria present; maintained by serial subculture;
Attributes
Authority(Kützing) Lange-Bertalot 1997
IsolatorGuillard (1956)
Collection Siteoyster pond Martha's Vineyard, Massachusetts, USA
Notes Name changed March 2022 after taxonomic revision, see AlgaeBase. This species is recommended for OECD Test Guideline 201 which calls for a freshwater medium. This strain, grown at CCAP in marine media, will grow in freshwater medium (DM either liquid or agar) but does not like continuous light.
Axenicity Status Bacteria present
Area North America
Country USA
Environment Marine
GMO No
Group Diatom
Pathogen Not pathogenic: Hazard Class 1
Special Uses used for ecotoxicity testing
Strain Maintenance Sheet SM_MarineDiatoms15_20.pdf
Toxin Producer Not Toxic / No Data
Type Culture No
Taxonomy WoRMS ID 149428
Equivalent StrainsCCMP543
Synonyms Navicula pelliculosa (Kützing) Hilse 1863
Formerly Listed in CCAP asNavicula pelliculosa

CCAP 1050/9

Fistulifera pelliculosa


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