Transport and cryopreservation of sperm of the common snook, Centropomus undecimalis (Bloch)

Sperm were collected in Florida from wild common snook, Centropomus undecimalis (Bloch), and were shipped to Louisiana State University for analysis and cryopreservation. Threshold activation of sperm (10% motility) occurred at 370 mOsmol kg^-1, and complete activation occurred at 680 mOsmol kg^-1. These values were significantly different. Sperm samples stored at 1(degree)C in Hanksʹ balanced salt solution (HBSS) or in 0.6% NaCl solution at 200 mOsmol kg-^1 retained motility for as long as 22 days. Mean motility remained above 50% for 9 days for sperm stored in HBSS and for 7 days for sperm stored in NaCl solution. Sperm exposed to 5% dimethyl acetamide (62+-10%; mean+-SD), 10% dimethyl sulphoxide (DMSO) (39+-16%), 5% glycerol (26+-5%) or 10% glycerol (6+-2%) for 30 min had significantly lower motility than did unexposed sperm (89+-9%). When used as a cryoprotectant, samples frozen with 5% or 10% DMSO or 5% methanol had significantly higher post-thaw motility than did samples frozen with other cryoprotectants. Sperm cryopreserved with 10% DMSO (38+-12%) had significantly higher post-thaw motility than did sperm cryopreserved with 15% DMSO (19 +-10%) or 20% DMSO (4+-4%). There were no significant differences in hatch rates of eggs fertilized with fresh sperm (54 +-29%) or cryopreserved sperm (41+-35%). Survival to first feeding was not different between fish produced with fresh sperm (37+-30%; range, 0-86%) or with thawed sperm (24+-29%; 0-77%). Transport of sperm to a cryopreservation laboratory and back to a hatchery for thawing and use enabled collaboration between groups with specific expertise and provides a model for the application of cryopreservation by transport of fresh and frozen samples Sperm were collected in Florida from wild common snook, Centropomus undecimalis (Bloch), and were shipped to Louisiana State University for analysis and cryopreservation. Threshold activation of sperm (10% motility) occurred at 370 mOsmol kg^-1, and complete activation occurred at 680 mOsmol kg^-1. These values were significantly different. Sperm samples stored at 1(degree)C in Hanksʹ balanced salt solution (HBSS) or in 0.6% NaCl solution at 200 mOsmol kg-^1 retained motility for as long as 22 days. Mean motility remained above 50% for 9 days for sperm stored in HBSS and for 7 days for sperm stored in NaCl solution. Sperm exposed to 5% dimethyl acetamide (62+-10%; mean+-SD), 10% dimethyl sulphoxide (DMSO) (39+-16%), 5% glycerol (26+-5%) or 10% glycerol (6+-2%) for 30 min had significantly lower motility than did unexposed sperm (89+-9%). When used as a cryoprotectant, samples frozen with 5% or 10% DMSO or 5% methanol had significantly higher post-thaw motility than did samples frozen with other cryoprotectants. Sperm cryopreserved with 10% DMSO (38+-12%) had significantly higher post-thaw motility than did sperm cryopreserved with 15% DMSO (19 +-10%) or 20% DMSO (4+-4%). There were no significant differences in hatch rates of eggs fertilized with fresh sperm (54 +-29%) or cryopreserved sperm (41+-35%). Survival to first feeding was not different between fish produced with fresh sperm (37+-30%; range, 0-86%) or with thawed sperm (24+-29%; 0-77%). Transport of sperm to a cryopreservation laboratory and back to a hatchery for thawing and use enabled collaboration between groups with specific expertise and provides a model for the application of cryopreservation by transport of fresh and frozen samples