Artemia Cysts - Brine Shrimp Eggs - Premium 260 Grade
High Grade 90% HR foil packed
Harvested from the Great Salt Lake (Utah, USA). Great Salt Lake EG260,000 NPG (90% hatch rate)
90% Hatch Rate
50g - Foil Pouch
100g - Foil Pouch
500g - Foil Pouch
1kg - vacuum packed foil Bag
What are the guidelines for Artemia cysts?
Salinity - 20 - 30 parts per thousand (ppt) salt solution or approximately 1-2 tablespoons of rock salt per quart (or liter) of water. This equates to around 1.015-1.020 specific gravity. A 20% (or around 1/2 teaspoon per quart) concentration of Epson salt or magnesium sulfate can be added to further buffer the hatching solution.
Temperature - Optimum temperature for a 24 hour complete hatch 26-28° C. Lowering the temperature would result in a longer hatching time. Do not exceed 30°C.
Light - Illumination is necessary to trigger the hatching mechanism within the embryo within the first few hours of incubation. Maintaining a light source during the entire incubation period is recommended to obtain optimum hatch results and for temperature control.
Aeration - Constant aeration is also necessary to provide sufficient oxygen levels for the cysts to metabolize and hatch. A minimum of 3 parts per million dissolved oxygen during the incubation is recommended. Strong aeration will not damage or hurt the brine shrimp cysts or nauplii.
pH - A starting pH of 8.0 or higher is recommended. If pH drops below 7.5 during incubation, add a teaspoon of sodium bicarbonate or a pH buffer to raise it above 8.0.
Stocking Density - 2 grams per quart or approximately one level tablespoon of cysts per quart is recommended. A higher stocking density will result in a lower % hatch.
Hatching Cone - Flat bottom hatching vessels should be avoided. Cone or "V" bottomed containers are best to insure that the cysts remain in suspension during hatching. Be sure to thoroughly wash the hatching cone with soap and water and allow to air dry between uses.
How do I harvest the baby brine shrimp?
To harvest the baby brine shrimp or nauplii, simply shut off the air and wait a few minutes for the shells and nauplii to separate. The shells will float to the surface and the live nauplii will go to the bottom of the cone towards the light source. Once separated, the nauplii can be siphoned from the bottom or drained from the bottom of the cone through the air tubing.