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I just bought 6 fish that will be arriving on my doorstep Wednesday morning from California.
My 20g long QT has been up and running fallow with a well-seeded sponge, HOB filter, Ammonia Badge, heater, powerhead, and light for 6 weeks. I’ve been ghost feeding every few days and ammonia is at zero. Temp is 76 and salinity is 0.19 – 0.20. I’m not trying for Hypo; I’m just keeping it low because it makes medications work better and provides more oxygen. Same for cooler temperatures.
Fish will have been in the bag for about 16-18 hours. They range from 1” to 2.5”. None are overly sensitive to copper or fresh water dips.
Here's my schedule:
1. When the fish arrive I plan to float for 30 minutes or so with the light turned off.
2. Then open each bag in a 5g bucket for drip acclimation for about an hour.
The fish are scared, tired, hungry and probably a little bit cold. I would like to do a freshwater dip and Rally bath BEFORE going into the QT. And I’d rather not use Prazi unless I really need to.
Now this is where I need your help. Help on Step #3.
3. For this step should I let them rest in buckets for a few hours (4-5 hours?) prior to doing the dip/bath? If not, when should I do the dip/baths? Remember these are tiny fish and very stressed out.
4. After the resting period, do 5 min freshwater dip in a black bucket to rule out flukes.
5. Do a 90 minute Rally bath to help dislodge any parasites and to provide instant relief and to help gills breathe easier.
6. Add fish to QT pre-dosed with Coppersafe at .5ppm and slowly ramp up to 2.0ppm over 3-4 days for two weeks. If I suspect velvet, speed up the level to 2.0ppm ASAP.
7. After 2 weeks in Cu, maybe do another fresh water dip prior to moving to observation to help remove some of the copper residue that might be still on the fish’s skin? Yes or no? Can’t hurt.
8. Remove fish from QT (Do not lower Cu level) and put in temporary holding bucket while breaking down QT for sterilization and airing out. I will put in a new seeded sponge from parasite-free DT. I need to reuse this same tank for observation.
9. Add clean non-medicated water to Observation Tank and spend at least 15 minutes each day watching for anything suspicious including bacterial infections. Slowly start to raise salinity and temperature to match DT. Observe for at least 2 weeks (3 is better).
10. If all are healthy and eating the fish will graduate to the display tank. Wheww! We made it. Glad that’s over!
Please, I'm open to any suggestions or comments!
Thanks,
Empress
My 20g long QT has been up and running fallow with a well-seeded sponge, HOB filter, Ammonia Badge, heater, powerhead, and light for 6 weeks. I’ve been ghost feeding every few days and ammonia is at zero. Temp is 76 and salinity is 0.19 – 0.20. I’m not trying for Hypo; I’m just keeping it low because it makes medications work better and provides more oxygen. Same for cooler temperatures.
Fish will have been in the bag for about 16-18 hours. They range from 1” to 2.5”. None are overly sensitive to copper or fresh water dips.
Here's my schedule:
1. When the fish arrive I plan to float for 30 minutes or so with the light turned off.
2. Then open each bag in a 5g bucket for drip acclimation for about an hour.
The fish are scared, tired, hungry and probably a little bit cold. I would like to do a freshwater dip and Rally bath BEFORE going into the QT. And I’d rather not use Prazi unless I really need to.
Now this is where I need your help. Help on Step #3.
3. For this step should I let them rest in buckets for a few hours (4-5 hours?) prior to doing the dip/bath? If not, when should I do the dip/baths? Remember these are tiny fish and very stressed out.
4. After the resting period, do 5 min freshwater dip in a black bucket to rule out flukes.
5. Do a 90 minute Rally bath to help dislodge any parasites and to provide instant relief and to help gills breathe easier.
6. Add fish to QT pre-dosed with Coppersafe at .5ppm and slowly ramp up to 2.0ppm over 3-4 days for two weeks. If I suspect velvet, speed up the level to 2.0ppm ASAP.
7. After 2 weeks in Cu, maybe do another fresh water dip prior to moving to observation to help remove some of the copper residue that might be still on the fish’s skin? Yes or no? Can’t hurt.
8. Remove fish from QT (Do not lower Cu level) and put in temporary holding bucket while breaking down QT for sterilization and airing out. I will put in a new seeded sponge from parasite-free DT. I need to reuse this same tank for observation.
9. Add clean non-medicated water to Observation Tank and spend at least 15 minutes each day watching for anything suspicious including bacterial infections. Slowly start to raise salinity and temperature to match DT. Observe for at least 2 weeks (3 is better).
10. If all are healthy and eating the fish will graduate to the display tank. Wheww! We made it. Glad that’s over!

Please, I'm open to any suggestions or comments!
Thanks,
Empress



