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February 15-18, 2009 Washington State Convention Center Seattle ...

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QUALITY ASSESSMENT OF ATLANTIC STURGEON Acipenser oxyrinchus SPERMATOZOA<br />

UNDER EXPERIMENTAL SHORT-TERM STORAGE CONDITIONS<br />

L. C. Woods III*, Katy Dorsey, Dan Theisen, Frank Siewerdt, Jerre Mohler, Brian Richardson, Glenn Welsh,<br />

Timothy Conn and David Guthrie<br />

Department of Animal and Avian Sciences<br />

University of Maryland<br />

College Park, MD 20742 USA<br />

There is significant interest to restore the Atlantic sturgeon, a species of concern. Biologists are interested in both the short-term<br />

storage and cryopreservation of semen to maximize availability of viable spermatozoa whenever a rare ripe female is found<br />

and available for spawning. We conducted short-term storage trials on semen obtained both from captive males, held at the<br />

US Fish and Wildlife Service’s Fish Technology <strong>Center</strong>, Lamar, Pennsylvania that were hormonally induced to spermiate; and<br />

wild males collected during the spawning season from the Hudson River this past year. Testes of all fish were catheterized to<br />

collect semen. Semen samples with motility at the time of collection > 90% were used in initial experiments to quantitatively<br />

examine cell quality over time under experimental conditions. Semen samples were stored under refrigeration (4 + 1oC) in two<br />

experimental gas environments: oxygen or nitrogen. Samples in each gas environment were additionally subdivided into three<br />

experimental dilutions: two experimental extenders and neat, or no dilution of the semen.<br />

Semen samples were collected from individual males and transported chilled, at 4-6 o C, to the lab. Upon arrival, analyses of<br />

gamete quality for each sample were performed prior to the administration of any experimental treatments. Approximately 24<br />

hours post-arrival (Day 1) and then every other day for one week (i.e. Day 3, 5, and 7), experimental semen samples were again<br />

quantitatively analyzed for quality. Sperm quality parameters evaluated included: motion analysis using a computer assisted<br />

sperm analysis system, viability using a flow cytometer, and cellular ATP levels using a Luciferin-Luciferase bioluminescence<br />

assay. Our results indicated that Atlantic sturgeon spermatozoa stored under oxygen retained higher quality than those stored<br />

in the absence of oxygen. One experimental diluent, appears to mediate the harmful effects of a storage environment that is<br />

without oxygen for up to one week.<br />

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