The purification of Cochlodinium. Sp and a comparative research on its mass cultivation
Cochlodinium is a dinoflagel that, with their bloom in the coastal water of worlds, can case fish mortality. Cochlodinium was detected in Persian Gulf, since 2008. After purification of C. polykricoides with light, the culture of cochlodinium, with medium of f/2 (modified), Guilard (f/2-Si), TMRL, Conway, ESM and the mixed of sea shore sediment with salt water (32 ppt) was done. The culture of cochlodinium in test tube, erlanmeyer with volume of 200-1000 ml and aquariums with the volume of 16 liter (each with 10 liter water) with three replicates in each treatment were done. Only the culture of cochlodinium with f/2 (modyfied) was possible in the aquarium. The culture of cochlodinium with TMRL medium in aquarium was not desirable and only in one aquarium from 3 aquariums, the density of cochlodinium reached to 910.000. cell per liter. The use of f/2 (modyfied) medium in the test tubes, and erlanmeyers, with the volume of 100-1000 ml, lead to suitable cochlodinium bloom. The maximum cell density in total treatments (with 3 replicates in each treatment) in test tube 3.283.000. cell (in 15 days), in erlanmeyer with 200 ml volume, 6.393.000. cells (in 22 days), in erlanmeyer with 500 ml volume, 2.833.000. cells (in 40 days) and in aquarium 3.600 .000. cells (in 46 days) counted. Cochlodinium culture with TMRL Medium in test tube and erlanmeyer was done successfully, but with the increase of erlanmeyer volume, the blooms of cochlodinium was lesser than f/2 (modyfied) medium. The maximum of cell count of TMRL Medium in test tube 2.683.000. cells (in 12 days), in erlanmeyer with 100 ml volume, 3.207.000. cells (in 36 days), in erlanmeyer with 250 ml 3.040.000. cells (in 18 days), in erlan with 1000 ml 2.325.000. cells (in 34 days) and in aquarium 550.000. cells (in 28 days) in each litre. Unsuccessful culture of cochlodinium with Conway medium, Gyllard (f/2-Si) and mixed salt water (32 ppt) with sea shore sediments, even in the test tube, indicated that these mediums weren’t suitablefor copchlodinium culture. With the increase of erlanmeyer volume, the success of ESM medium decreased. But, in test tube and in erlanmeye with 100 ml volum, was almost, successful. We can concluded that, cochlodinium culture required, special condition and medium, that in f/2 (modyfied) medium the culture of cochlodinium was successful. The maximum cochlodinium cell count was 6.5 million per liter in one aquarium. The mean of 3 replicate of this treatment was 3.600.000. cells per liter with f/2 (modified) medium. For culture of cochlodinium polykricoides, the f/2 (modyfied) medium was better than others mediums.
| Main Authors: | , , , , , , , , , , |
|---|---|
| Format: | monograph biblioteca |
| Language: | Persian |
| Published: |
Iranian Fisheries Science Research Institute
2013
|
| Subjects: | Ecology, Iran, Persian Gulf, Cochlodinium, Different culture mediums, Cell density, Laboratory condition, Purification, Cochlodinium.sp, Dinoflagel, Mortality, C. polykricoides, Culture, Aquarium, Sediments, Cochlodinium polykricoides, |
| Online Access: | http://hdl.handle.net/1834/39784 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|