scholarly journals Reconciling nuclear microsatellite and mitochondrial marker estimates of population structure: breeding population structure of Chesapeake Bay striped bass (Morone saxatilis)

Heredity ◽  
2005 ◽  
Vol 94 (6) ◽  
pp. 606-615 ◽  
Author(s):  
K M Brown ◽  
G A Baltazar ◽  
M B Hamilton
2020 ◽  
Vol 226 ◽  
pp. 105506 ◽  
Author(s):  
Isaac Wirgin ◽  
Lorraine Maceda ◽  
Matt Tozer ◽  
Joseph Stabile ◽  
John Waldman

2010 ◽  
Vol 90 (3) ◽  
pp. 181-189
Author(s):  
MA Matsche ◽  
A Overton ◽  
J Jacobs ◽  
MR Rhodes ◽  
KM Rosemary

2020 ◽  
Vol 13 (6) ◽  
pp. 1468-1486 ◽  
Author(s):  
Nathalie M. LeBlanc ◽  
Benjamin I. Gahagan ◽  
Samuel N. Andrews ◽  
Trevor S. Avery ◽  
Gregory N. Puncher ◽  
...  

1976 ◽  
Vol 54 (4) ◽  
pp. 449-462 ◽  
Author(s):  
I. Paperna ◽  
D. E. Zwerner

Information on the distribution, life cycle, and seasonal abundance of the copepod Ergasilus labracis Krøyer, parasitic on the gills of lower Chesapeake Bay striped bass, Morone saxatilis (Walbaum), is presented after a 12-month survey. The overall prevalence of E. labracis was 90% in all localities sampled and it was found to be as euryhaline as its host; it has been found in salinities from 0.l‰ to 32.0‰. E. labracis was present and reproductively active throughout the year, suffering only a temporary slowdown in egg production at the beginning of the winter. Peak invasion of striped bass gills by infective larvae occurred during April and May; minor peaks were also recorded during July and October. The free-living stage was estimated to last as long as 6 weeks during early spring. Duration of other developmental stages was also extrapolated. Attempts to rear larvae in the laboratory past the metanauplius stage failed. Larvae could be kept for a maximum of 23 days after hatching if fed nannoplankton and kept at 20 °C in river water of 16–18‰.


2012 ◽  
Vol 69 (3) ◽  
pp. 430-446 ◽  
Author(s):  
E.J. Martino ◽  
E.D. Houde

Abundance of age-0 striped bass ( Morone saxatilis ) exhibits 50-fold variability in Chesapeake Bay. Processes that act to reduce and thus regulate this variability were investigated. The potential for density-dependent regulation of growth and mortality in the early juvenile stage and its causes were investigated. Data from multiple seine and trawl surveys in upper Chesapeake Bay and tributaries were analyzed to construct growth and mortality indices having a high degree of spatial and temporal resolution. Age-0 mean lengths in September were inversely related to density, ranging from 67.8 mm in 1994, when mean density was 0.036·m–2, to 104.5 mm in 1992, when mean density was 0.003·m–2. Except for the Potomac River, evidence for density-dependent growth was consistent across subpopulations. Bioenergetics modeling indicated that prey consumption was limiting except in low-abundance years. Mortality increased with respect to abundance and also was density-dependent. The significant interaction between age-0 juvenile length in September and subsequent winter temperature on mortality indicated that density-dependent growth leads to size-selective overwinter mortality. A statistical model including age-0 abundances, age-0 lengths, and winter temperature explained a substantial fraction of variability and the mechanisms for regulation of striped bass recruitment.


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