Spawning of the American Shad, Alosa sapidissima in the Lower Connecticut River

1972 ◽  
Vol 13 (2) ◽  
pp. 116 ◽  
Author(s):  
Barton C. Marcy
1972 ◽  
Vol 29 (10) ◽  
pp. 1495-1499 ◽  
Author(s):  
Raymond C. Levesque ◽  
Roger J. Reed

Food habits of young American shad (Alosa sapidissima) were studied in the Connecticut River above Holyoke, Massachusetts, 1969. Diurnal feeding data revealed a peak in stomach content volume at 8:00 PM during midsummer. Larval shad fed mainly on aquatic crustaceans and tendipedid larvae and pupae. Juveniles ingested the most abundant organisms: crustaceans, tendipedid larvae and pupae, hydropsychid larvae and adult insects. Electivity data indicated positive selection for tendipedid pupae and crustaceans and negative selection for hydropsychid larvae and tendipedid larvae. Selection of Trichoptera larvae by young shad in significant amounts was documented for the initial time.


1973 ◽  
Vol 30 (12) ◽  
pp. 1847-1860 ◽  
Author(s):  
Julian J. Dodson ◽  
William C. Leggett

The migratory behavior of American shad (Alosa sapidissima) approaching their natal river during the final saltwater stage of the spawning migration was studied using ultrasonic tracking and conventional tagging procedures. Initial displacement of most sonic-tagged shad released without displacement adjacent to and 10 km west of the Connecticut River was not in the direction of the home river. These fish, however, homed successfully to the Connecticut River as did dart-tagged shad released in the same areas.Shad exhibited two major behavior patterns; countercurrent orientation in response to the reversing tidal current and adjustment of swimming speed to changes in tidal velocity. Countercurrent orientation was equally significant during daylight and darkness, whereas the adjustment of swimming speeds to tidal current velocity was more significant during daylight than darkness.Shad tracked to the west exhibited a westerly bias inherent in the basic open water behavior patterns. Shad exhibited a greater degree of directed movement when oriented against the ebb tide and adjusted their swimming speeds to exceed the ebb tide velocity and to approximately equal the flood tide velocity. Shad tracked to the east exhibited the same major behavior patterns but with the opposite directional bias.A hypothesis is presented suggesting that the location of the home river is achieved by means of a nonrandom search. Environmental clues indicative of the Connecticut River act to establish a preferred direction of displacement while the actual unidirectional displacement is achieved by reference to the rate and direction of tidal currents.


1990 ◽  
Vol 47 (8) ◽  
pp. 1570-1577 ◽  
Author(s):  
Michael H. Prager ◽  
Mary C. Fabrizio

We examined the applicability of logistic regression to stock identification studies and compared its performance on two data sets to that of linear and quadratic discriminant functions. Logistic regression can be used to model a categorical dependent variable associated with continuous or discrete independent variables, and is preferred to discriminant analyses when the explanatory variables are not multivariate normal. Our examples were American shad (Alosa sapidissima) from the Connecticut River and Hudson River estuaries, and striped bass (Morone Saxatilis) from the Hudson River, Chesapeake Bay, and Roanoke River estuaries. In the examples we used a resampling method to assess classification and allocation errors of the two methods on new data. For the shad data, the logistic model classified significantly more fish correctly, and provided a significantly better estimate of stock composition. For the striped bass data, the two methods classified about the same proportion of fish correctly, but the logistic model gave a significantly better estimate of stock composition.


1985 ◽  
Vol 42 (10) ◽  
pp. 1640-1648 ◽  
Author(s):  
Victor A. Crecco ◽  
Thomas F. Savoy

We examined the hypothesis that temporal oscillations in zooplankton abundance, river flows, and temperatures in the Connecticut River affect the survival and growth rates of larval and juvenile American shad, Alosa sapidissima, among 5-d cohorts. The relative survival rates between newly hatched shad larvae and juveniles were low among early cohorts (May 21 – June 15), but rose rapidly among later cohorts (June 21 – July 6) when river flows were low and temperatures and zooplankton densities were high. Age of larval and juvenile shad was estimated by counting daily rings on sagittal otoliths and age-specific length increments determined by backcalculation techniques. Cohort-specific growth rates of larval shad increased linearly with rising zooplankton densities, and asymptotically with rising river temperatures and declining flows. By contrast, juvenile growth rates among 5-d cohorts showed no significant linear or nonlinear relationships to water temperatures and flows.


1984 ◽  
Vol 41 (8) ◽  
pp. 1216-1223 ◽  
Author(s):  
Victor A. Crecco ◽  
Thomas F. Savoy

We evaluated a parent–progeny relationship for Connecticut River shad, Alosa sapidissima, with population data from 1966 through 1982. The hypothesis that shad year-class strength is established during larval development mainly by abiotic factors was assessed by correlation analysis between environmental variables, year-class strength, weekly zooplankton densities, hydrographic conditions, and larval feeding success among the 1979 through 1982 year-classes. No significant parent–progeny relationship was found for American shad even after recruitment variations due to river flow and water temperatures were removed. All three environmental variables (mean river discharge, water temperatures, and total monthly precipitation) were significantly correlated with shad year-class strength for the month of June, the period when most American shad larvae emerge.


1971 ◽  
Vol 28 (8) ◽  
pp. 1167-1171 ◽  
Author(s):  
William C. Leggett ◽  
Robert A. Jones

During tracking of 13 adult American shad (Alosa sapidissima) with ultrasonic transmitters in 49 approaches to commercial drift gillnets in the lower Connecticut River, only one shad was captured. Typically, shad moved to within 1–2 m of the net before sensing its presence, then turned and swam along the net, close to the mesh, to its end, where they turned and continued their upriver migration. Sight appeared to play an important role in net detection. However, 14 avoidances were observed when light intensities were inadequate to allow visual detection of the mesh. It was concluded that other senses, perhaps the lateral line, also function in net avoidance, especially when sight is impaired.


1983 ◽  
Vol 40 (10) ◽  
pp. 1719-1728 ◽  
Author(s):  
V. Crecco ◽  
T. Savoy ◽  
L. Gunn

Age-specific growth and survival rates were estimated for larval and juvenile American shad (Alosa sapidissima) from the Connecticut River from 1979 to 1982. Relative indices (CPE) of year-class strength of juveniles determined from seine sampling in 1978–82 and 1966–73 are compared with resulting levels of adult recruitment. Length–age data for larval and juvenile American shad were determined from sagittal otoliths. Length increments among larval and juvenile shad followed an asymptotic pattern with age, both life stages being well described by the Gompertz equation. Larval survivorship curves from 1979 to 1982 were age specific, with mortality rates of 19.8–25.6%/d for first feeding larvae and 4.3–8.7%/d for larvae approaching metamorphosis. By contrast, juvenile mortality rates were much lower (1.8–2.0%/d) and more consistent among years. Juvenile indices of year-class strength from 1966 to 1973 were positively correlated (r = +0.92, df 7, P < 0.001) with recruitment levels of adult females 4–6 yr later, suggesting that year-class strength of shad is established prior to the juvenile stage.


1999 ◽  
Vol 56 (7) ◽  
pp. 1159-1171 ◽  
Author(s):  
Jill BK Leonard ◽  
Stephen D McCormick

We examined total and tissue-specific energy content of upstream-migrating American shad (Alosa sapidissima) in the Connecticut River. Total energy depletion over the course of the 228-km migration ranged from 35 to 60%. The approximate contributions of different tissues to energy use during migration were white muscle 57%, subdermal fat 27%, red muscle 8%, viscera 6%, and liver 2%. American shad preferentially use energy stores in the skin and its subdermal fat layer (depleted by 63%) while sparing red muscle protein. Both lipid and protein were used as energy sources throughout migration, although lipids were depleted to a greater extent (e.g., white muscle lipid decreased 48% and protein 30%). Large fish expended 2-21% more energy during migration than small fish. Migrating to upriver sites (198-228 km) is 50-100% more energetically expensive than to lower river sections for females. This suggests that upriver range expansion may be limited by females in that they may have reached a threshold level of energy expenditure in this upriver area. American shad may possess physiological mechanisms for tissue-specific energy use allowing maintenance of critical tissues necessary for postspawning survival.


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