Another Phytoplankton Culture Tutorial

This is a day 14 update. Both tanks are lighter since I just doubled the amount of salt water. I did the same last week. I also doubled the amount of F2 each time. I did remove some to feed the copepods. One more week and each tank will be full then I can use a larger amount to feed them and keep it going if all goes well.

Splitting into two seems to be the right thing since one tank is definitely doing better than the other. I did have to increase the airflow. The deeper it gets the more air is needed. I have made it a habit to shake each tank every other day so I do not get any growth stuck to the walls.

This is using cheap 1 gallon plastic containers from Walmart, bottom LED lighting for growing and a 3D printed base. I also 3D printed a holder for the solid airline to connect it to the lid that is easily removable. At the top of the solid airline is a valve to adjust the air.

phyto_starting_day14.jpg
 
This is a day 14 update. Both tanks are lighter since I just doubled the amount of salt water. I did the same last week. I also doubled the amount of F2 each time. I did remove some to feed the copepods. One more week and each tank will be full then I can use a larger amount to feed them and keep it going if all goes well.

Splitting into two seems to be the right thing since one tank is definitely doing better than the other. I did have to increase the airflow. The deeper it gets the more air is needed. I have made it a habit to shake each tank every other day so I do not get any growth stuck to the walls.

This is using cheap 1 gallon plastic containers from Walmart, bottom LED lighting for growing and a 3D printed base. I also 3D printed a holder for the solid airline to connect it to the lid that is easily removable. At the top of the solid airline is a valve to adjust the air.

phyto_starting_day14.jpg
Yepp, always split in multiple smaller batches and always keep a backup for a few days. Preferably in the fridge.

Just to show how lazy you can get with Nannochlorpsis: The batch I started is still running, no water added, no fertilizer, culture still pure and dense. I'm currently trying to get a Tetra culture running from a crashed starter I received. It will take a while but I might get there... We will see. If it worked I will post here and explain what I did (it isn't too much different or complicated).

I might also soon show how you can use certain substances to stain phyto cultures to see if the cells are still alive or if you are basically dealing with dead particles. I will have to see if I can find the time.
 
Is it a very bad idea to premix 25 L of sea water, add hypochlorite and store in a dark place?
It would make staring a new culture so much quicker. Just fill the vessels, squirt F2 and sodium thiosulfate via sub micron filter and good to go.
I am writing this in the middle of the night when it was 2 days I simply had no time to mix and sterilise.
 
Hey there so today I harvested my secknd batch of phyto using some of the first batch. I used 2 seperate containers one came out darker than the other however there is some bubbling/foaming at the top of the lighter one has this gone bad? Is it safe to dose and or use as another starter culture?
20260819_101028.jpg
20260819_101600.jpg
 
Is it a very bad idea to premix 25 L of sea water, add hypochlorite and store in a dark place?
It would make staring a new culture so much quicker. Just fill the vessels, squirt F2 and sodium thiosulfate via sub micron filter and good to go.
I am writing this in the middle of the night when it was 2 days I simply had no time to mix and sterilise.
Good question... I know that chlorine will gas out over time so it's possible that after a while it loses potency, but if the container is air tight, doesn't have much headroom, and can withstand a potential pressure build up (I don't think there will be much pressure though) it should work.

I would dechlorinate first before adding F2 to be honest. The chlorine might react with the fertilizer otherwise.
 
Hey there so today I harvested my secknd batch of phyto using some of the first batch. I used 2 seperate containers one came out darker than the other however there is some bubbling/foaming at the top of the lighter one has this gone bad? Is it safe to dose and or use as another starter culture?
20260819_101028.jpg
20260819_101600.jpg
I would use the darker one as starter culture, but it's still safe to dose in my opinion, as long as it doesn't smell like absolute death 😅

I keep backup cultures that I often neglect and after they crash, I still use them to feed my corals. They would catch detritus in the wild as well, I don't think they mind.
 
Good question... I know that chlorine will gas out over time so it's possible that after a while it loses potency, but if the container is air tight, doesn't have much headroom, and can withstand a potential pressure build up (I don't think there will be much pressure though) it should work.

I would dechlorinate first before adding F2 to be honest. The chlorine might react with the fertilizer otherwise.
I will do and report.
 
Question about Tetraselmis: The cells clump and drop each time I start a new culture. Last 2 times I was really careful to match salinity and temperature, bubbled air for 12h before inoculation, and it still ended up at the bottom.
The cells re-suspend and partially de-clump when I manually mix the new culture, and all is fine after 2 days of babysitting. I am not sure if the cells permanently re-suspend though, as some green 'sediment' remains. But the culture takes off and all is good without any further manual agitation. Is this normal? I checked the culture under a scope and I could see only Tetra cells, nothing else.
 
Question about Tetraselmis: The cells clump and drop each time I start a new culture. Last 2 times I was really careful to match salinity and temperature, bubbled air for 12h before inoculation, and it still ended up at the bottom.
The cells re-suspend and partially de-clump when I manually mix the new culture, and all is fine after 2 days of babysitting. I am not sure if the cells permanently re-suspend though, as some green 'sediment' remains. But the culture takes off and all is good without any further manual agitation. Is this normal? I checked the culture under a scope and I could see only Tetra cells, nothing else.
This is a common "issue" as far as I know. Usually Tetraselmis are flagellated cells that move very fast on their own, but when introduced into a new media they might still end up reacting with a stress response where they become non-motile and drop to the bottom. Non-motile cells are relatively large and dense so they are hard to keep suspended. Shaking the culture in the first few days from time to time should get the job done until the so called "lag phase" where reproduction seems to stall is over. As long as the culture increases in density afterwards it should be fine. Maybe the sudden change in nutrients when entering a new culture vessel is already enough for the stress response, I don't know.
 
I've had good results with Nanno. Today started Tetra in 2 separate small pods. So let's see how that goes. My air bubbles for Nanno go wild, but Tetra requires a gentle bubbling as I understand. Probably closer to what copepods would get? But otherwise it's the same process as Nanno, right? Same amount of F/2?

What's the next culture to try after Tetra so I can start looking into that? I'd like to start mixing colors.
 
I've had good results with Nanno. Today started Tetra in 2 separate small pods. So let's see how that goes. My air bubbles for Nanno go wild, but Tetra requires a gentle bubbling as I understand. Probably closer to what copepods would get? But otherwise it's the same process as Nanno, right? Same amount of F/2?

What's the next culture to try after Tetra so I can start looking into that? I'd like to start mixing colors.
F/2 works for Tetraselmis.

Synechococcus (a "good" cyanobacterium) is quite easy to keep and often recommended to get rid of cyano problems in tanks (I don't know if it's an effective treatment though).

Then there is Rhodomonas salina and "Isochrysis galbana" which has been reclassified to Tisochrysis lutea I believe but you will most likely find it as Isochrysis.
 
F/2 works for Tetraselmis.

Synechococcus (a "good" cyanobacterium) is quite easy to keep and often recommended to get rid of cyano problems in tanks (I don't know if it's an effective treatment though).

Then there is Rhodomonas salina and "Isochrysis galbana" which has been reclassified to Tisochrysis lutea I believe but you will most likely find it as Isochrysis.
I'm intrigued by Rhodomonas salina. You think it's a good match for Nanno and Tetra? In terms of balancing the nutrients each offers. Are Nanno and Tetra - for all intents and purposes - interchangeable? (I'm basing this question on nothing but their color!)
 

IF YOU HAD TO OPERATE EVERYTHING ELSE MANUALLY, WHICH AUTOMATED SYSTEM WOULD YOU KEEP?

  • Auto top-off

    Votes: 62 58.5%
  • Automated dosing

    Votes: 6 5.7%
  • Mechanical filtration / roller filter

    Votes: 4 3.8%
  • Automated water testing

    Votes: 3 2.8%
  • Automatic feeding

    Votes: 1 0.9%
  • Lighting schedule

    Votes: 20 18.9%
  • Controller and remote monitoring

    Votes: 4 3.8%
  • Leak detection and emergency shutoff

    Votes: 2 1.9%
  • Automatic water changes

    Votes: 3 2.8%
  • None. I prefer to operate everything manually

    Votes: 0 0.0%
  • Something else (explain in the comments)

    Votes: 1 0.9%
Back
Top
Home
Post thread…
Market
What's new