Algal Culturing Techniques 2005
DOI: 10.1016/b978-012088426-1/50027-5
|View full text |Cite
|
Sign up to set email alerts
|

Recipes for Freshwater and Seawater Media

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
245
0
7

Year Published

2008
2008
2017
2017

Publication Types

Select...
9
1

Relationship

0
10

Authors

Journals

citations
Cited by 278 publications
(254 citation statements)
references
References 0 publications
2
245
0
7
Order By: Relevance
“…In culture, it reaches 1.5 mm in body length and has a generation time of about 18 days. In mass cultures, worms are maintained at 208C in glass Petri dishes containing f/2 medium (Andersen et al 2005) and fed with the diatom Nitzschia curvilineata. The worm is fairly transparent, allowing non-invasive measurement of morphological traits such as body size, testis size, ovary size and seminal vesicle size (Schärer & Ladurner 2003).…”
Section: Methodsmentioning
confidence: 99%
“…In culture, it reaches 1.5 mm in body length and has a generation time of about 18 days. In mass cultures, worms are maintained at 208C in glass Petri dishes containing f/2 medium (Andersen et al 2005) and fed with the diatom Nitzschia curvilineata. The worm is fairly transparent, allowing non-invasive measurement of morphological traits such as body size, testis size, ovary size and seminal vesicle size (Schärer & Ladurner 2003).…”
Section: Methodsmentioning
confidence: 99%
“…Several cultures were established but only two were kept and grown in 50 ml culture flasks. The strain IFR-MLO-01M was grown in K medium (Keller et al, 1987) while the second strain IFR-MLO-02M was grown in f/2 medium (Guillard & Ryther, 1962;Andersen et al, 2005). Both strains were maintained in a growth chamber set up at 22 ± 1.0°C and a 12 : 12 light: dark illumination cycle with~50 µmol photons m −2 s −1 provided by white fluorescent tubes.…”
Section: Sampling and Cultivationmentioning
confidence: 99%
“…Cell cultures of Micractinium conductrix strain Pbi (formerly Chlorella strain Pbi) were grown in FES medium (Reisser et al, 1986), while cultures of Chlorella heliozoae strain SAG 3.83 were grown in modified Bold's basal medium (Van Etten et al, 1983), and Chrysochromulina parva were grown in DY-V medium (Anderson et al, 2005). Viral lysates were generated for ATCV-1, CVM-1 and CpV-BQ1 by inoculating 1 ml of infectious viruses (i.e., 0.45-μm-filtered viral lysates) into 150 ml cultures of the appropriate host.…”
Section: Cell Culture Conditions and Estimating Virus Titersmentioning
confidence: 99%