scholarly journals Use of gill nets and telemetry in tracking movements and feeding of striped bass (Morone saxatilis), bluefish (Pomatomus saltatrix), and weakfish (Cynoscion regalis) at a salinity front in a small estuary

2017 ◽  
Vol 115 (2) ◽  
pp. 143-154
Author(s):  
Linda L. Stehlik ◽  
John P. Manderson ◽  
Jeffrey Pessutti
1995 ◽  
Vol 52 (8) ◽  
pp. 1647-1666 ◽  
Author(s):  
Kyle J. Hartman ◽  
Stephen B. Brandt

Bioenergetics models for striped bass (Morone saxatilis), bluefish (Pomatomus saltatrix), and weakfish (Cynoscion regalis) were developed from laboratory experiments on metabolism and consumption. Size-specific rates of consumption and metabolism were similar for bluefish and weakfish and higher than those for striped bass. Temperature effects on maximum consumption rate (Cmax) differed with fish size. Cmax of young fish (30 g) increased with temperature, then declined rapidly at higher temperatures; Cmax for larger fish of all three species (100–3000 g) increased rapidly to the maximum rate, but leveled off at higher (25–30 °C) temperatures. Results of Cmax experiments suggest that extrapolation of the temperature dependency of small fish to larger fish, as is commonly done, may misrepresent potential growth at higher temperatures. Independent model validation using laboratory experiments found consumption estimates (from growth) to be within −1.4 to +4.5% of known values for all species at temperatures above 19 °C; however, at 6.9°C consumption by striped bass was overestimated by 20–46%. Model estimates of growth (from consumption) were within −7.1 to +30.1% of known values in all validations. Overall, the growth physiology of the three species appeared to be related to the water temperatures encountered during estuarine residency and production.


1999 ◽  
Vol 56 (2) ◽  
pp. 275-287 ◽  
Author(s):  
Jeffrey A Buckel ◽  
David O Conover ◽  
Nancy D Steinberg ◽  
Kim A McKown

We measured bluefish (Pomatomus saltatrix) weights, densities, and prey sizes during the summers of 1992 and 1993 and diets over a 4-year period (1990-1993) in the Hudson River estuary. This information was used to estimate the loss of young-of-the-year (YOY) striped bass (Morone saxatilis) resulting from YOY bluefish predation. We then compared this predation mortality with the total loss of striped bass in the system. Data from sampling surveys conducted since the mid-1970's were used to examine relationships between bluefish abundance and striped bass recruitment levels. YOY striped bass, bay anchovy (Anchoa mitchilli), Atlantic silverside (Menidia menidia), and Alosa spp. dominated YOY bluefish diets. There were ontogenetic and interannual differences in YOY bluefish diets. Bluefish avoided striped bass at low densities but selected for them at high densities, suggesting a density-dependent feeding response. In the early summer of 1993, bluefish predation accounted for 50-100% of the total estimated loss of YOY striped bass. A significant negative correlation exists between the relative magnitude of striped bass recruitment and bluefish abundance. We conclude that YOY bluefish are important predators of estuarine fish and can have a substantial impact on their recruitment.


1979 ◽  
Vol 83 (1) ◽  
pp. 217-230
Author(s):  
M. A. FREADMAN

1. Striped bass and bluefish use cyclic ventilatory movements to accomplish gas exchange at rest and slow swimming speeds, whereas at intermediate and high velocities, both species routinely shift to ram gill ventilation. 2. Metabolic characteristics of the shift in respiratory behaviour indicate that as an animal adopts the ram mode, energy expenditure departs from an exponential relationship and increases at a shallow rate over the next 15 cm. S−1 range in speed. At higher, ram-supporting velocities, oxygen uptake increases once again at an exponential rate. 3. Similar determinations of oxygen uptake at imposed swimming velocities in hatchery-raised rainbow trout reveal an exponential relationship over the entire swimming range. Trout actively ventilate their gills over this velocity range as well. 4. In striped bass, the requisite trans-gill pressure for ram ventilation, as developed between the mouth and opercular door margins, is about 05 cm H2O. 5. Critical swimming velocities for striped bass are 2.9–3.3 bl.s−1 while bluefish can maintain station at 4.0–4.6 bl.S−1. 6. The adoption of ram gill ventilation is a velocity-dependent phenomenon over the size-range tested. 7. Transfer of the work load of ventilation from the branchial to the swimming musculature results in substantial metabolic savings well within the cruising ranges of striped bass and bluefish. The savings probably accrue from cessation of rhythmic pumping by the branchial musculature and a change in overall body drag at ram-supporting swimming speeds.


2020 ◽  
Vol 142 ◽  
pp. 47-53
Author(s):  
K Béland ◽  
G Séguin ◽  
S Lair

An unusually high mortality rate due to verminous (Philometra rubra) coelomitis was documented in wild-hatched striped bass Morone saxatilis raised in a fish hatchery as part of a stock restoration program. To decrease the parasitic burden and therefore potentially minimize mortality, the effectiveness of 2 different anthelmintics was evaluated. Two trials were conducted on wild-collected fingerlings naturally infected by P. rubra. In 2006, 144 yearling fish were randomly assigned to 4 experimental groups: (1) levamisole (Levasol®) at 2 mg l-1 via immersion for 8 h once weekly for 3 wk; (2) levamisole at a dose of 2.5 mg kg-1 biomass via feed once daily for 7 d; (3) emamectin benzoate (Slice®) at a dose of 0.05 mg kg-1 biomass via feed once daily for 7 d; and (4) control. Emamectin successfully eliminated live nematodes in 84.9% of the fish, whereas the administration of levamisole, either via immersion or feed, was not successful in significantly reducing the number of live P. rubra. In 2007, the administration of the same dosage of emamectin to approximately 1000 naturally infected yearling striped bass was associated with a 100% mortality rate of P. rubra in the 30 fish randomly examined 5 wk after the beginning of the treatment. Results of these trials indicate that, at the dosage used, the administration of emamectin at the end of the summer is safe for striped bass yearlings and considerably reduces the prevalence and intensity of the infection by this parasite.


2019 ◽  
Vol 41 (4) ◽  
pp. 507-520 ◽  
Author(s):  
L Vanalderweireldt ◽  
P Sirois ◽  
M Mingelbier ◽  
G Winkler

Abstract After being extirpated from the St. Lawrence River in the 1960s, striped bass (Morone saxatilis) were reintroduced to the estuary in 2002 and by 2008, they were naturally reproducing. To document the habitat use and feeding ecology of this reintroduced population, we examined the gut contents of 333 larvae and juveniles. Samples were collected in four estuarine habitats in 2014: the upstream freshwater section (UP), the oligohaline (O-ETM) and the mesohaline (M-ETM) estuarine turbidity maximum zones, and the downstream polyhaline section (DOWN). In June, pelagic larvae developed in the UP and the O-ETM, feeding mainly on copepods such as Eurytemora affinis. The O-ETM exhibited better suitable feeding conditions compared to the UP, likely due to the presence of Bosmina sp. as a primary prey. After July, striped bass shifted to larger prey items, consuming mainly dipteran pupa in upstream littoral habitats and gammarids and mysids in downstream habitats. In the early summer, the UP provided a high-quality nursery habitat and as the season progressed, the smallest juveniles dispersed downstream and improved their feeding success by exploiting a new feeding niche. This observation suggests that being distributed throughout the estuary may increase the potential survival of striped bass early life stages.


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