Quantifying the combined effects of attempt rate and swimming capacity on passage through velocity barriers
T Castro-Santos - Canadian Journal of Fisheries and Aquatic …, 2004 - cdnsciencepub.com
The ability of fish to migrate past velocity barriers results from both attempt rate and
swimming capacity. Here, I formalize this relationship, providing equations for estimating the …
swimming capacity. Here, I formalize this relationship, providing equations for estimating the …
Beyond Ucrit: matching swimming performance tests to the physiological ecology of the animal, including a new fish 'drag strip'
JA Nelson, PS Gotwalt, SP Reidy… - … and Physiology Part A …, 2002 - Elsevier
Locomotor performance of animals is of considerable interest from management,
physiological, ecological and evolutionary perspectives. Yet, despite the extensive …
physiological, ecological and evolutionary perspectives. Yet, despite the extensive …
Swimming performance traits of twenty-one Australian fish species: a fish passage management tool for use in modified freshwater systems
Freshwater ecosystems have been severely fragmented by artificial in-stream structures
designed to manage water for human use. Significant efforts have been made to reconnect …
designed to manage water for human use. Significant efforts have been made to reconnect …
Swimming performance of sauger (Sander canadensis) in relation to fish passage
DR Dockery, TE McMahon… - Canadian journal of …, 2017 - cdnsciencepub.com
A lack of information on the swimming abilities of sauger (Sander canadensis), a highly
migratory species particularly sensitive to habitat fragmentation, may inhibit the design of …
migratory species particularly sensitive to habitat fragmentation, may inhibit the design of …
Facilitating upstream passage of small-bodied fishes: linking the thermal dependence of swimming ability to culvert design
EM Rodgers, RL Cramp, M Gordos… - Marine and …, 2014 - CSIRO Publishing
Fish passage through road culverts is poorly understood, particularly for small-bodied fishes,
despite this information being integral to the restoration of waterway connectivity. We …
despite this information being integral to the restoration of waterway connectivity. We …
Swimming efficiency of the white crappie, Pomoxis annularis
GR Parsons, JL Sylvester Jr - Copeia, 1992 - JSTOR
Swim tunnel respirometry was utilized to study metabolic rate and swimming efficiency in
white crappie, Pomoxis annularis. We examined oxygen consumption (V̇O2) at various …
white crappie, Pomoxis annularis. We examined oxygen consumption (V̇O2) at various …
Critical swimming capacity of the Atlantic silverside,Menidia menidia L.
SI Hartwell, RG Otto - Estuaries, 1991 - Springer
Critical swimming speed was determined for the Atlantic silverside (Menidia menidia) at
several time and velocity increments. Fish were tested at time increments (Δt) of 2, 5, 10, 15 …
several time and velocity increments. Fish were tested at time increments (Δt) of 2, 5, 10, 15 …
Optimal swim speeds by respirometer: an analysis of three neotropical species
EMF Viana, PS Pompeu, CB Martinez - Neotropical Ichthyology, 2012 - SciELO Brasil
The swimming ability of neotropical fish species is an important aspect for fish ladder
designs. Especially in Latin America, where fish ladders are highly selective, fish strategies …
designs. Especially in Latin America, where fish ladders are highly selective, fish strategies …
Effect of temperature on swimming performance in juvenile southern catfish (Silurus meridionalis)
The critical swimming speed (Ucrit, aerobic swimming performance) and endurance
(anaerobic swimming performance) of juvenile southern catfish Silurus meridionalis Chen …
(anaerobic swimming performance) of juvenile southern catfish Silurus meridionalis Chen …
Effect of temperature on swimming performance of sea bass juveniles
G Koumoundouros, DG Sfakianakis… - Journal of Fish …, 2002 - Wiley Online Library
At four temperatures (T= 15, 20, 25 and 28° C) swimming performance of Dicentrarchus
labrax was significantly correlated with total length (23–43 mm LT); r2= 0.623–0.829). The …
labrax was significantly correlated with total length (23–43 mm LT); r2= 0.623–0.829). The …