Interactions between bluefish and striped bass: Behavior of bluefish under size- and number-impaired conditions and overlap in resource use

A decline in bluefish (Pomatomus saltatrix L.) recreational landings during the 1990s and the early 2000s led to multiple theories on the ultimate cause. One theory was that a large portion of the bluefish population moved offshore and was unavailable to nearshore recreational fishers; one reason given for the movement offshore was increased competition with striped bass (Morone saxatilis W.). We conducted laboratory experiments (feeding and non-feeding) to examine behavioral interactions between adult bluefish and sub-adult striped bass in a large (121,000 L) research aquarium. Additionally, we examined diet and habitat overlap of bluefish and striped bass from the fall and spring bottom trawl surveys conducted by the National Marine Fisheries Service. Observations of feeding trials for the following treatments were made: non-impaired (i.e., same number and size of bluefish and striped bass), size-impaired (i.e., large striped bass/small bluefish), number-impaired (i.e.,10 striped bass/3bluefish), and single-species controls. Within a species, there was no difference in a variety of behavioral measures (e.g., attack rate, capture success, ingestion rate, and activity) between mixed- and control treatments under non-impaired or size-impaired conditions. However, behavior of number-impaired bluefish differed from control and size-impaired fish suggesting that striped bass may have a negative influence on bluefish foraging when bluefish are “out-numbered”. Feeding had a strong effect on swimming speeds for both species. Diet and habitat overlap between bluefish and striped bass in continental shelf waters was low. Overall, foraging behavior in mixed-species treatments and field observations suggest no competitive interactions between adult bluefish and sub-adult striped bass.     

Modelling swimming activities and energetic costs in European sea bass (Dicentrarchus labrax L., 1758) during critical swimming tests

Muscular activity patterns in red and white muscles linked to oxygen consumption were studied during critical swimming tests in the sea bass (Dicentrarchus labrax Linnaeus 1758). The species is one of the most important for Mediterranean Sea aquaculture. A sigmoid model was used to fit both the oxygen consumption and red muscle activity while the white muscle activity pattern was described by an exponential model. Red muscle reaches an activation plateau close to critical swimming speed mostly due to the oxygen diffusion velocity in tissues. The exponential activation of white muscle appears to be linked to short and sudden periods of great energy need to cope with adverse conditions such as predation and escape. Both oxygen consumption and muscular activity were found to be size dependent. The bioenergetics of sea bass was modelled based on fish mass and swimming speed to predict the minimum and maximum speed as well as the mass-specific active metabolic rate and standard metabolic rate. An important finding was that contrary to other well-known species, swimming at subcritical speeds in sea bass involves both red and white muscle in different proportions.     

Biochemical responses to temperature in the contractile protein complex of striped bass Morone saxatilis

The effects of acute and long-term changes in temperature upon catalytic and calcium regulatory function of red (slow oxidative) and white (fast glycolytic) muscle from striped bass (Morone saxatilis) were determined. Acclimation to 5 degrees C or 25 degrees C had no significant effect on catalytic function (ATPase activity) or regulatory sensitivity (Ca++-activation) of myofibrils from either muscle type. Substantial differences between red and white muscle were found in the intrinsic thermal sensitivity of maximally-activated Mg++-Ca++ myofibrillar ATPase. Arrhenius plots of myofibrillar ATPase from white muscle show one significant breakpoint at 29 degrees C, with activation energies (Ea) of 2.3 and 23.4 kcal mole-1 at temperatures above and below this transition, respectively. Arrhenius plots of myofibrillar ATPase from red muscle show two transitions occurring at 22 and 9 degrees C, with Ea of 7.6 kcal mole-1 above 22 degrees C and 18.3 kcal mole-1 between 9 and 22 degrees C. Activation energies for myofibrils from red muscle increase substantially to approximately 107.3 kcal mole-1 below the 9 degrees C breakpoint. Differences in the intrinsic thermal sensitivity of red and white muscle catalytic function are apparently due to interaction of actomyosins and calcium regulatory proteins which are specific to each muscle type. The results suggest that capacity for sustained swimming in striped bass, which is powered exclusively by red muscle, will be severely impaired at cold temperature unless compensations occur above the level of contractile proteins.     

Red and white muscle fibre activity in swimming skipjack tuna, Katsuwonus pelamis (L.)

To test the hypothesis that white muscle fibre portions of the myotomes are used at sustainable swimming speeds, skipjack tuna, Katsuwonus pelamis , were forced to swim against various current velocities in a water tunnel while electrical activity of the red and white muscle fibres was simultaneously recorded. Eight fish were tested, five fish graded white muscle fibres into activity at swimming speeds above their minimum hydrostatic equilibrium speed, but well below the estimated maximum sustainable swimming speed of skipjack tuna. Three other fish showed white muscle fibre activity at minimum swimming speeds, a possibly abnormal condition.     

Allometric scaling of maximal enzyme activities in the axial musculature of striped bass, Morone saxatilis (Walbaum)

It had been suggested that the activity of anaerobic enzymes in the white muscle of fish increases exponentially with body size to meet the increasing hydrodynamic costs of burst swimming. We tested whether this relationship holds across a very large size range of striped bass, spanning a nearly 3,000-fold range in body mass. We examined the scaling of marker enzymes of anaerobic (lactate dehydrogenase and pyruvate kinase) and aerobic (citrate synthase and malate dehydrogenase) metabolism in the red and white locomotor muscles. In white muscle, we found positive scaling of anaerobic enzymes only in smaller fishes. Positive scaling of anaerobic enzymes was not found among the samples that included fishes >1,000 g despite having a sufficiently large sample size to detect such scaling. The absence of positive scaling in the white muscles of large bass suggests that they are unable to generate sufficient power to sustain relative burst swimming performance. Enzymes from aerobic pathways had activities that were mass independent in both red and white muscle. Red and white muscles were metabolically distinct except among the smallest fishes. Among young of the year, the anaerobic capacity of red muscle approached that of white muscle and also showed positive scaling. This unusual pattern suggests that red muscle might augment white muscle during burst swimming and add to the total power generated by these small fish. Maximizing burst swimming performance may be critical for small fishes vulnerable to predation but unimportant for large fishes.     

Muscle activity in steady swimming scup, Stenotomus chrysops, varies with fiber type and body position

The red and pink aerobic muscle fibers are used to power steady swimming in fishes. We examined red and pink muscle recruitment and function during swimming in scup, Stenotomus chrysops, through electromyography and high-speed ciné. Computer analysis of electromyograms (EMGs) allowed determination of initial speed of muscle recruitment and duty cycle and phase of muscle electromyographic activity for both fiber types. This analysis was carried out for three longitudinal positions over a range of swimming speeds. Fiber type and longitudinal position both affected swimming speed of initial recruitment. Posterior muscle is recruited at the lowest swimming speed, whereas more anterior muscle is not initially recruited until higher speeds. At more anterior positions, the initial recruitment of pink muscle occurs at a higher swimming speed than the recruitment of red muscle. The duty cycle of pink muscle EMG activity is significantly shorter than that of red muscle, reflecting a difference in the onset time of activation during each cycle of length change: pink muscle onset time follows that of red. The different patterns of usage of red and pink muscle reflect differences in their contraction kinetics. Because pink muscle generates force more rapidly than red muscle, it can be activated later in each tailbeat cycle. Pink muscle is used to augment red muscle power production at higher swimming speeds, allowing a higher aerobically based steady swimming speed than that possible by red muscle alone.     

Sustained swimming speeds and myotomal muscle function in the trout, Salmo gairdneri

Rainbow trout were trained for 3–4 weeks in a flume at swimming speeds of 1, 2 and 3 l s⁻¹. For each experiment growth rates were estimated and by measuring the hypertrophy of red and mosaic skeletal muscle fibres their function was described at particular swimming speeds and compared with earlier experiments on coalfish using the same technique.
Maximum growth, compared with controls in still water, occurred at swimming speeds of 1 l s⁻¹. At this speed the trout mosaic muscle fibres hypertrophied by 40% but the red muscle fibres showed only a 25% hypertrophy. It is suggested that natural swimming speeds are close to 1Ls^−l and the trout mosaic fibres are better adapted for use at this speed in comparison with coalfish white muscle fibres.     

Power isn't everything: muscle function and energetic costs during steady swimming in Atlantic cod (Gadus morhua)

Power produced by red myotomal muscles of fish during cruise swimming appears seldom maximized, so we sought to investigate whether economy may impact or dominate muscle function. We measured cost of transport (COT) using oxygen consumption and the strain trajectories and electromyographic activity of red muscle measured at anterior (ANT) and posterior (POST) locations while Atlantic cod (Gadus morhua) swam steadily at speeds between 0.3 and 1.0 body lengths (BL) s(-1). We then measured the power produced by isolated segments of red muscle when activated either as in the swimming cod or such that maximal net power was produced. Patterns of activation during swimming were not optimal for power output and were highly variable between tail beats, particularly at the ANT location and at slow swim speeds. Muscle strain amplitude did not increase until swimming speed reached 0.9 (ANT) versus 0.5 (POST) BL s(-1). These limited power to only 53% (ANT) and 71% (POST) of maximum at slower swim speeds and to 70%-80% of maximum at high swim speeds. COT (resting metabolism subtracted) was minimal at the slowest swim speed, surprisingly, where power was most impaired by activation and strain. Thus, production of powered forces for maneuverability/stability appeared to greatly impact red muscle function during cruise swimming in cod, particularly at slow speeds and in ANT muscle.     

Red muscle function during steady swimming in brook trout, Salvelinus fontinalis.

Red muscle function during steady swimming in brook trout was studied through both in vivo swimming and in vitro muscle mechanics experiments. In the swimming experiments, red muscle activity was characterized through the use of electromyography and sonomicrometry, allowing the determination of several parameters such as tailbeat frequency, EMG burst duration, muscle length change patterns and relative phase of EMG activity and length change. Brook trout do show some shifts in these variables along their length during steady swimming, but the magnitude of these shifts is relatively small. In the muscle mechanics experiments, the in vivo muscle activity data were used to evaluate patterns of power production by red muscle during swimming. Unlike many fish species, the red muscle along the length of brook trout shows little change in isometric kinetic variables such as relaxation rate and twitch time. Furthermore, there is no rostral-caudal shift in red muscle mass-specific power output during steady swimming. This last result contrasts sharply with rainbow trout and with a variety of other fish species that power steady swimming primarily with the posterior red myotome.     

A study of the swimming performance of the Crucian carp Carassius carassius (L.) in relation to the effects of exercise and recovery on biochemical changes in the myotomal muscles and liver

A study has been made of the maximum sustained swimming speed of Crucian carp Carassius carassius (L.) using a fixed velocity technique. The data obtained from swimming tests on 214 carp have been analysed using the method of probit analysis. The 50% fatigue level for 13–16 cm fish acclimated to 9.5±0.6°C has been estimated to be 3.35 lengths/sec. Biochemical measurements have been made on the red and white myotomal muscles and liver of fish subjected to both varying intensities of sustained swimming and short periods of vigorous swimming. Free creatine was found to increase only during high speed swimming in the white muscle. Elevated lactate concentrations occurred at both low and high sustained swimming speeds in the red superficial muscle but not during short periods of strenuous exercise. Glycogen depletion from the red musculature also only took place at the sustained swimming speeds investigated. The reverse situation was operative in the white muscle, significant glycogen depletion occurring only at the highest swimming speed studied. Lactate levels were only significantly different from non-exercised fish in the fish swimming at the higher velocities. The effects of periods of recovery following 200 min of sustained swimming were also investigated. White muscle lactate was at a higher level than non-exercise fish 5 h post-exercise, while both red muscle glycogen and lactate rapidly returned to pre-exercise concentrations. Biochemical measurements on the myotomal muscle types have been discussed in relation to the swimming performance of the fish and the division of labour between red and white fibres.     

Postexercise physiology and repeat performance behaviour of free-swimming smallmouth bass in an experimental raceway

We studied postexercise physiology and behaviour of smallmouth bass (Micropterus dolomieu) that voluntarily ascended experimental raceways of varying length (20-50 m) against water velocities ranging from 8 to 120 cm/s. Our first objective was to link mean swimming speed to metabolism using patterns in postexercise muscle glycogen, muscle lactate, and plasma lactate. Our second objective was to examine several behavioural indices (attempt rate, success rate, and recovery time between an ascent and a subsequent attempt) and determine whether patterns in these data reflected those from the physiological measurements. Postexercise muscle glycogen and plasma lactate data suggest that smallmouth bass powered swimming speeds up to 70-80 cm/s using energy from aerobic processes. However, lactate did not begin to accumulate in the white muscle until speeds in excess of 120-130 cm/s were reached. The behavioural parameters measured did not indicate the presence of a physiological threshold at 70-80 cm/s; however, patterns in all factors changed appreciably when fish maintained speeds in excess of 120-130 cm/s. Therefore, it is clear that behaviour and physiology are tightly linked in this species and that maximum aerobic swimming capacity may not limit performance (or re-performance) during short-duration swims.     

Red muscle recruitment during steady swimming correlates with rostral-caudal patterns of power production in trout

Rainbow trout (Oncorhynchus mykiss) and brook trout (or charr, Salvelinus fontinalis) display different rostral-caudal patterns of power production by the red or aerobic muscle during steady swimming. The anterior muscle of rainbow trout produces much less power for swimming than the posterior, while in brook trout there is no variation in power output. To determine if red muscle recruitment is associated with anterior-posterior patterns of power production, electromyography (EMG) was used to record red muscle activity at three body positions across a range of swimming speeds in fish of each species. The initial recruitment of the anterior red muscle in swimming rainbow trout was predicted to lag behind, i.e. occur at higher speeds, that of the posterior due to the variation in power production, but no variation in recruitment was expected for brook trout. Burst of red muscle EMG activity occurring with each tailbeat was analyzed for frequency (tailbeat frequency), duty cycle (DC) (duration of burst relative to the period of the tailbeat) and burst intensity (BI) (magnitude of the measured EMG activity). Brook trout swam with higher tailbeat frequencies and longer values of DC than rainbow trout. Both species showed a pattern of longitudinal variation in DC, with longer DC values in the anterior red muscle. BI also differed significantly along the length of rainbow trout but not brook trout. In the former, BI of anterior muscle was significantly less than the posterior at lower steady swimming speeds. The EMG data suggest that power production and muscle recruitment are related. In rainbow trout, where there is longitudinal variation in muscle power output, there are also significant rostral-caudal differences in red muscle recruitment.     

Measurement of larval striped bass (Morone saxatilis) net avoidance using evasion radius estimation to improve estimates of abundance and mortality

Net avoidance rate increases as a function of larval striped bass size. This causes under-estimation of abundance and overestimation of mortality rate. We modeled net avoidance by assuming that fish avoid the net by swimming a radial distance at a right angle to the net axis. This distance, the evasion radius, was estimated by comparing the calculated densities of striped bass larvae from a series of paired tows involving a large and a small net. Iteration and solution models were used to estimate the evasion radius for each millimeter size group of fish in order to estimate the actual density in the environment. Avoidance of the nets increased with fish length. The ratio of actual density in the environment to the measured density in the small net was used to adjust abundances measured in our ichthyoplankton surveys. After adjusting for net avoidance, mortality rates of striped bass larvae from the Sacramento-San Joaquin Estuary were reduced by 10% compared to the unadjusted rates.      

Importance of electrode positioning in biotelemetry studies estimating muscle activity in fish

Red and white axial muscle activity of adult Atlantic salmon Salmo salar was examined using conventional electromyography (EMG x ) and activity radio-transmitters (EMG i ) at 0·5 and 0.7 body lengths (L) along the body of the fish. Critical swimming trials were conducted and maximum sustainable speeds (U_crit) were unaffected by the presence of electrodes, being 1·51 ± 21 m s⁻¹ (3.33 ± 0.34 L s⁻¹) ( n =44). Regardless of longitudinal position of the electrodes within the musculature, both EMG x s and EMG i s indicated increasing red muscle activity with increasing swimming speed, whereas white muscle fibres were recruited only at speeds > 86±5% U_crit. Telemetered EMG i signals indicated that muscle activity varied significantly for electrodes implanted at different longitudinal positions along the fish ( P < 0·001). These results suggest that electrode placement is an important influence affecting the signals obtained from radio transmitters that estimate activity and location should be standardized within biotelemetry studies to allow accurate and consistent comparisons of activity between individuals and species. Optimal location for electrode placement was determined to be in the red muscle, towards the tail of the fish (0·7 L ).     

Role of aerobic and anaerobic circular mantle muscle fibers in swimming squid: electromyography

Circular mantle muscle of squids and cuttlefishes consists of distinct zones of aerobic and anaerobic muscle fibers that are thought to have functional roles analogous to red and white muscle in fishes. To test predictions of the functional role of the circular muscle zones during swimming, electromyograms (EMGs) in conjunction with video footage were recorded from brief squid Lolliguncula brevis (5.0-6.8 cm dorsal mantle length, 10.9-18.3 g) swimming in a flume at speeds of 3-27 cm s(-1). In one set of experiments, in which EMGs were recorded from electrodes intersecting both the central anaerobic and peripheral aerobic circular mantle muscles, electrical activity was detected during each mantle contraction at all swimming speeds, and the amplitude and frequency of responses increased with speed. In another set of experiments, in which EMGs were recorded from electrodes placed in the central anaerobic circular muscle fibers alone, electrical activity was not detected during mantle contraction until speeds of about 15 cm s(-1), when EMG activity was sporadic. At speeds greater than 15 cm s(-1), the frequency of central circular muscle activity subsequently increased with swimming speed until maximum speeds of 21-27 cm s(-1), when muscular activity coincided with the majority of mantle contractions. These results indicate that peripheral aerobic circular muscle is used for low, intermediate, and probably high speeds, whereas central anaerobic circular muscle is recruited at intermediate speeds and used progressively more with speed for powerful, unsteady jetting. This is significant because it suggests that there is specialization and efficient use of locomotive muscle in squids.     

Estimating piscine prey size from partial remains: testing for shifts in foraging mode by juvenile bluefish

Knowledge of prey sizes consumed by a predator aids in the estimation of predation impact. Young-of-the-year bluefish, Pomatomus saltatrix, attack their prey tail-first and often bite their prey in half; this poses a unique problem in determining prey sizes from stomach content analysis. We developed a series of linear regressions to estimate original prey lengths from measurements of eye diameter and caudal peduncle depth for striped bass, Morone saxatilis, bay anchovy, Anchoa mitchilli, American shad, Alosa sapidissima, blueback herring, Alosa aestivalis, Atlantic silverside, Menidia menidia, and white perch, Morone americana. We then used these regressions to estimate original prey sizes from pieces of prey found in stomachs of bluefish collected in the Hudson River estuary from 1990–1993. Lengths of prey that were swallowed whole were compared to estimated lengths of prey that were consumed in pieces. Lengths of prey that were consumed in pieces were larger than prey that were consumed whole. We determined the prey length/predator length ratio at which bluefish began shifting from swallowing their prey whole to partial consumption. Shifting occurred at a ratio of approximately 0.35 irrespective of prey species, suggesting that prey length plays an important role in predator foraging decisions and may contribute to gape limitations. Shifts in foraging mode effectively reduce gape limitation and allow bluefish to consume larger prey sizes which may increase their effect on prey populations.     

How swimming fish use slow and fast muscle fibers: implications for models of vertebrate muscle recruitment

We quantified the intensity and duration of electromyograms (emgs) from the red and white axial muscles in five bluegill sunfish (Lepomis macrochirus) which performed three categories of behavior including steady swimming and burst and glide swimming at moderate and rapid speeds. Steady swimming (at 2 lengths/s) involved exclusively red muscle activity (mean posterior emg duration = 95 ms), whereas unsteady swimming utilized red and white fibers with two features of fiber type recruitment previously undescribed for any ectothermic vertebrate locomotor muscle. First, for moderate speed swimming, the timing of red and white activity differed significantly with the average onset time of white lagging behind that of red by approximately 40 ms. The durations of these white emgs were shorter than those of the red emgs (posterior mean = 82 ms) because offset times were effectively synchronous. Second, compared to steady and moderate speed unsteady swimming, the intensity of red activity during rapid unsteady swimming decreased while the intensity of white muscle activity (mean white emg duration = 33 ms) increased. Decreased red activity associated with increased white activity differs from the general pattern of vertebrate muscle recruitment in which faster fiber types are recruited in addition to, but not to the exclusion of, slower fiber types.     

Sensitivity of North American sturgeons and paddlefish to fishing mortality

Sturgeons and paddlefish exhibit unusual combinations of morphology, habits, and life history characteristics, which make them highly vulnerable to impacts from human activities, particularly fisheries. Five North American sturgeons (shortnose, Gulf, pallid, Alabama, and green sturgeon) are listed as endangered or threatened by management authorities. Managers have instituted fishery closures for the three other species of North American sturgeons (Atlantic, white, and shovelnose) and paddlefish because of low stock abundance at some point in this century. Reproductive potential in four species I examined (Atlantic, white, and shortnose sturgeon, and paddlefish) is more sensitive to fishing mortality than it is for three other intensively-fished coastal species in North America: striped bass, winter flounder, and bluefish. The sturgeons and paddlefish are generally longer-lived than the three other coastal species, and also have an older age at full maturity, lower maximum fecundity values, and older ages at which 50% of the lifetime egg production is realized with no fishing mortality.     

Lesion induction by the plerocercoid Lacistorhynchus tenuis (Cestoda) and wound healing in the striped bass Morone saxatilis (Walbaum)

San Francisco Bay-Delta striped bass, Morone saxatilis (Walbaum), form open lesions in response to a plerocercoid infection of Lacistorhynchus tenuis (Van Beneden, 1858) (Cestoda: Trypanorhyncha). Laboratory infection experiments showed that striped bass can be infected with the plerocercoids by ingesting infected copepods. Histological sections indicated that a cellular host response was mounted early in the infection period, and that despite the leucocytic infiltration the parasites continued to develop. However, at 3 months post-infection some of the plerocercoids began to degenerate, and lesions formed at this time and 14 months post-infection. Open lesions in adult striped bass collected from the field took 2 months to heal and were detectable for at least 22 months. Regeneration of the muscle tissue did not occur although the wound completely healed externally.