|Document Type:||Master's Thesis|
|Name:||Matthew Alan Patterson|
|Title:||Energy Reserves in Native Freshwater Mussels (Bivalvia:Unionidae) with and without Attached Zebra Mussels: Effects of Food Deprivation.|
|Degree:||Master of Science|
|Committee Chair:||Dr. Bruce C. Parker|
|Committee Members:||Dr. Richard J. Neves, Co-Chair|
|Dr. Alan Heath|
|Keywords:||Unionids, Zebra Mussels, Glycogen, Gut Contents, Assimilation, Quarantine|
|Date of defense:||June 5, 1998|
|Availability:||Release the entire work for Virginia Tech access only.
After one year release worldwide only with written permission of the student and the advisory committee chair.
This project evaluated the feasibility of salvaging zebra mussel-infested freshwater mussels from their native habitat by determining 1) how zebra mussel infestation affects unionid feeding and body condition, 2) how starvation in quarantine affects body condition of unionids, and 3) what feeding regime maintain unionid condition in quarantine.
The effects of zebra mussel infestation on two mussel species were evaluated through glycogen analyses of mantle tissue and gut content analysis. Specimens of Amblema p. plicata (Say, 1817) and Quadrula p. pustulosa (I. Lea, 1831), collected from a heavily infested reach of the Ohio River in 1996, had significantly lower (p<0.05) glycogen levels than specimens collected from a low-infestation reach upstream. In 1996 and 1997, heavily infested Amblema p. plicata and Quadrula p. pustulosa had significantly less (p<0.01) organic matter and fewer algal cells in their guts than lightly infested specimens. In addition, gut contents of individual A. p. plicata contained significantly less (p<0.05) organic matter and fewer algal cells than the combined gut contents of all zebra mussels (18-33 mm in length) attached to their shells. Gut analyses also revealed significant diet overlap between native unionids and infesting zebra mussels. Thus, competitive interactions or interference by zebra mussels likely reduced unionid ingestion and consequently reduced glycogen stores.
During quarantine, unionids salvaged from a lightly infested area and starved for 30 days had glycogen levels that declined dramatically. After 30 days without supplemental feeding, mean glycogen levels of A. p. plicata declined 85%, and mean glycogen levels of Q. p. pustulosa declined 70%. Thus, feeding of unionids is necessary to maintain their condition during lengthy quarantine.
To determine the best feeding regime for unionids in quarantine, assimilation efficiencies and carbon budgets were established for the rainbow mussel, Villosa iris (Lea, 1829), using radio-labelled cultures of Neochloris oleoabundans (Chantanachat and Bold 1962) at three cell concentrations. Assimilation efficiencies for Villosa iris at 100,000cells/ml, 10,000 cells/ml, and 1,000 cells/ml were similar (45-56%); however, regardless of these similarities, assimilation efficiencies from this study indicate that Neochloris oleoabundans is readily assimilated (~50% AE) by Villosa iris . In addition, total assimilation was maximized at 100,000cells/ml, which indicates that Villosa iris has the greatest amount of energy available for growth, reproduction, and maintenance of condition in captivity at this cell concentration.
During a second quarantine experiment, specimens were provided with 100,000cells/ml of N. oleoabundans twice per day. Initial mean glycogen levels for Amblema p. plicata (9.4 + 2.4 mg/g) and Quadrula p. pustulosa collected from ORM 175.5 in July 1997 were not significantly different (p>0.3) than the mean glycogen levels of A. p. plicata and Q. p. pustulosa collected from the same site in July 1996. Glycogen stores of unionids entering quarantine, therefore, were similar in both the starvation and controlled feeding experiments. After 7, 14, and 30 days of controlled feeding in quarantine, mean glycogen levels of A. p. plicata and Q. p. pustulosa did not change significantly (p>0.1). Thus, quarantine protocol for salvaged native mussels should include the feeding of algae to captive specimens to sustain glycogen levels prior to relocation.
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