Seasonal activities of Barbus barbus: effect of temperature on time-budgeting

Surgically implanted activity-circuit radio transmitters (40 MHz) were used to study the seasonal activities of 21 adult (males: 23 to 35 cm f.l. and females 38 to 55 cm f.l. ) Barbus barbus (Pisces, Cyprinidae) in the River Ourthe (Southern Belgium) in 1989–1991. During the autumnal thermal transition (water temperature 9 to 10° C), the typical dusk and dawn pattern observed in summer turned to a trimodal pattern with the emergence of a diurnal phase. The auroral then crepuscular and finally diurnal activity periods progressively vanished as water temperature decreased down to the thermal limit for activity (4.0° C), when barbel entered a dormancy period. An opposite progressive shift was observed during the spring thermal transition. Daily activity budgets ranged from 0 to 720 min—on the annual cycle and were significantly ( r ²=0.686, P <0.05, d.f. = 36) dependent on water temperature and on morphodynamic unit size, while fish size was non-significant. Although the dusk and dawn rhythm pattern was consistent throughout summer, water temperature significantly ( P <0.05) interfered with the respective duration of crepuscular and auroral activities ( r ²=0.586, d.f. = 57 and r ²=0.692, d.f. = 55). The precise timing of activities was also thermal-related and the activities of small male barbel were proportionally more nocturnal than those of large female barbel (ANCOVA, F =80.61, d.f. = 31 and F =4.s5, d.f. = 23, at dusk and dawn respectively), possibly due to predation pressure on small fish. It is concluded that the seasonal variations of activity budgets, rhythm patterns and timings in B. barbus correspond to a form of time-budgeting partly to achieve thermal homeostasis in a variable environment.     

Laboratory studies on the effects of thermal change on the behaviour and distribution of juvenile chum salmon in sea water

Schooling chum salmon Oncorhynchus keta were biased towards the water surface (median position <1 m) under isothermal conditions (10° C) in a water column simulator (WCS). Thermal stratification (24/10° C) inhibited upward movement with fish congregating at the thermocline and displaying a clear avoidance of potentially lethal surface waters. A tri-phase model based on piece-wise nonlinear regression was used to describe the distribution shifts of chum salmon during a change from isothermal to thermally stratified conditions. Fish distribution was consistent with thermoregulatory behaviour and exhibited 'attraction', 'preference' and 'avoidance' phases. The thermal preference of 50% of the fish lay between 12·2 and 20·2° C, however, >83·5% of the fish occupied a 'preferred' temperature range of 13·7–17·9° C. The mean temperature at which 50% of chum salmon avoided rising temperature by shifting deeper in the water column and using the cooler thermocline was 20·2° C, and 90% avoidance occurred at 22·9° C. Behavioural responses to thermal stratification were consistent amongst underyearling fish of differing size and age.     

Rate of energy depletion and overwintering mortality of juvenile walleye pollock in cold water

The winter energy deficit and mortality of juvenile walleye pollock at extremely cold temperature were examined by field observations and laboratory experiments. In the Doto area, along the northern coast of Japan, juvenile walleye pollock resided on the continental shelf despite extremely cold temperatures (mean 0·4° C) during the latter half of winter (March to April). Measurements of the rate of energy depletion (equivalent to the routine metabolic rate) revealed that juvenile walleye pollock consumed 37% less energy at 0·5° C than at 2·0° C, suggesting an energetic benefit of residence in cold water (<1·0° C) over the shelf during winter. Prior to the starvation experiments, temperatures and ration level in the holding tanks were adjusted to create two different body condition groups of fish. Under the thermal condition of the latter half of winter (0·5° C), fish with a mean condition factor of 0·6 and 0·5 suffered 19·1 and 74·5% mortality, respectively, at the end of the experiments (after 56 days). The residual analysis of total body energy demonstrated that the cause of mortality was mainly associated with the depletion of energy reserves. When a logistic regression model for mortality derived from the experiments was applied to wild fish collected in March, the estimated overwintering mortality in 2004 and 2005 was 25·4 and <2·3%, respectively, assuming no feeding during the winter. Considering that juvenile walleye pollock feed during winter as shown in previous studies, intense overwintering mortality induced by energy depletion is improbable during the latter half of winter in the Doto area.     

Thermal acclimation of swimming performance in newt larvae: the influence of diel temperature fluctuations during embryogenesis

1.  Thermal acclimation is one of the basic strategies by which organisms cope with thermal heterogeneity of the environment. Under predictable variation in environmental temperatures, theory predicts that selection favours acclimation of thermal performance curves over fixed phenotypes.
2.  We examined the influence of diel fluctuations in developmental temperatures on the thermal sensitivity of the maximal swimming capacity in larvae of the alpine newt, Triturus alpestris .
3.  We incubated newt eggs under three thermal regimes with varying daily amplitudes (1, 5 and 9 °C) and similar means (17·6–17·9 °C), and accordingly we measured the swimming speed of hatched larvae at three experimental temperatures (12, 17 and 22 °C), which they would normally experience in their natural habitat.
4.  Embryonic development under low and middle temperature fluctuations produced larvae with similar swimming speeds across experimental temperatures. In contrast, the most fluctuating regime induced development of phenotypes, which at 12 °C swam faster than larvae developed under moderate diel fluctuations.
5.  Our results provide evidence that diel temperature fluctuations induce acclimation of thermal dependence of locomotor performance. In ectotherms experiencing diel cycles in environmental temperatures, this plastic response may act as an important pacemaker in the evolution of thermal sensitivity.     

Reproductive biology of the threatened golden galaxias Galaxias auratus Johnston and the influence of lake hydrology

Golden galaxias Galaxias auratus (31–235 mm fork length, L _F) were collected monthly from littoral habitats in Lakes Crescent and Sorell, Tasmania, Australia, between July 2000 and December 2002. Spawning habitats were identified and monitored in both lakes, and surveyed in Lake Crescent. Trends in gonado-somatic indices and reproductive stages of development indicated that gonad development in both sexes begins in midsummer and peaks in late autumn to early winter. Males mature at smaller sizes (50% at 52 mm L _F) than females (50% at 76 mm L _F), larger individuals are predominately females (95% of fish ≥138 mm L _F), and overall male to female ratios are female biased ( c . 1:2). Spawning occurs late autumn to early spring (water temperatures = 1·4–9·7° C) with peaks in spawning activity in winter (mean water temperatures <5° C). Demersal adhesive eggs ( c. 1·5 mm diameter) were found on cobble substrata ( c. 20–250 mm diameter) in littoral areas ( c. 0·2–0·6 m deep) and fecundity of fish 71–181 mm L _F ranged from 619 to 14 478 eggs. The rate of change in water level over the 20 days prior to monthly sampling was important in explaining the occurrence of spent fish and this accounted for temporal differences in spawning between the populations. Lake hydrology influences the reproductive cycle of G. auratus by possibly providing a stimulus for spawning and it controls the availability of spawning habitat in Lake Crescent. Seasonal hydrological cycles ( i.e. rises during late autumn to winter) and a minimum water level of 802·20 m Australian Height Datum in Lake Crescent during autumn (above which littoral areas of cobble substratum are inundated) are critical to G. auratus populations.     

Thermal tolerance of a northern population of striped bass Morone saxatilis

Thermal tolerance of age 0+ year Shubenacadie River (Nova Scotia, Canada) striped bass Morone saxatilis juveniles (mean ± s . e . fork length, L _F, 19·2 ± 0·2 cm) acclimated in fresh water to six temperatures from 5 to 30° C was measured by both the incipient lethal technique (72 h assay), and the critical thermal method ( C _m). The lower incipient lethal temperature ranged from 2·4 to 11·3° C, and the upper incipient lethal temperature ( I _U) from 24·4 to 33·9° C. The area of thermal tolerance was 618° C². In a separate experiment, the I _U of large age 2+ year fish (34·4 ± 0·5 cm L _F) was 1·2 and 0·6° C lower ( P < 0·01) than smaller age 1+ year fish (21·8 ± 0·5 cm L _F) at acclimation temperatures of 16 and 23° C. Using the C _m, loss of equilibrium occurred at 27·4–37·7° C, loss of righting response at 28·1–38·4° C and onset of spasms at 28·5–38·8° C, depending on acclimation temperature. The linear regression slopes for these three responses were statistically similar (0·41; P > 0·05), but the intercepts differed (25·3, 26·0 and 26·5° C; P < 0·01). The thermal tolerance of this northern population appears to be broader than southern populations.     

Survival of Listeria monocytogenes in sea water and effect of exposure on thermal resistance

Survival, recoverability and sublethal injury of two strains of Listeria monocytogenes , Scott A and an environmental strain KM, on exposure to sea water at 12·8 or 20·8 °C was determined using in situ diffusion chambers. Plate counts were used to assess recoverability and injury while 5-cyano-2,3-ditolyl tetrazolium chloride (CTC) reduction was used to determine respiratory activity. T₉₀ values (times for 10-fold decreases in numbers of recoverable cells) on non-selective medium (trypticase soya agar with 0·6% yeast extract) at 12·8 and 20·8 °C were 61·7 and 69·2 h for L. monocytogenes Scott A, and 103·0 and 67·0 h for L. monocytogenes KM, respectively. On selective medium (Oxford agar), T₉₀ values at 12·8 and 20·8 °C were 60·6 and 56·9 h for L. monocytogenes Scott A, and 83·0 and 65·9 h for L. monocytogenes KM, respectively. With Scott A, the percentage of sublethally injured cells at 12·8 and 20·8 °C was 1·7 and 17·7%, respectively, while for KM the values were 19·0 and 1·6%, respectively. The fraction of cells reducing CTC but which were not recoverable on plating progressively increased on exposure to sea water. Listeria monocytogenes KM challenged at 58 °C showed an apparent increase in heat resistance after exposure to sea water at 20·8 °C for 7 d ( D ₅₈= 2·64 min) compared with before exposure ( D ₅₈= 1·24). This increase in thermal resistance was not apparent at temperatures greater than 63 °C, and analysis of the best-fit regression lines fitted to the thermal data obtained from the two cell populations indicated that their thermal resistance was not significantly different ( P > 0·05) over the temperature range tested (58–62 °C).     

Compensatory growth of juvenile brown flounder Paralichthys olivaceus (Temminck & Schlegel) following thermal manipulation

The compensatory growth of juvenile brown flounder Paralichthys olivaceus (body mass c. 12 g) following different thermal exposure was investigated. Fish were exposed to one of the five temperatures: 8·5 ( T _8·5), 13·0 ( T _13·0), 17·5 ( T _17·5), 22·0 ( T _22·0) and 26·5° C ( T _26·5) for 10 days and fish grew best at 22·0° C. Then the water temperature in all treatments was equably adjusted to 22·0° C over 3 days. At the end of the following 30 days after temperature adjustment, there were no significant differences between body masses of fish in the different treatments (wet body mass at the end of the experiment ranged from 22·13 to 24·56 g). Results indicated that the juvenile P. olivaceus achieved complete compensatory growth. Analysis of the dynamics of the feeding rates and feed conversion efficiencies indicated that compensatory growth of the fish experienced low temperature ( T _8·5, T _13·5 and T _17·5) or high temperature ( T _26·5) exposure was mainly dependent on increasing feed intake (hyperphagia) and possibly by improvement in feed conversion efficiency. The moisture content was not affected by different temperature exposure significantly. The lipid and energy content of juvenile P. olivaceus in T _8·5, however, were significantly lower than other treatment. Results of the current study indicate that a short period of low or high temperature exposure may not affect annual growth, but may affect lipid and energy deposition.     

Reproductive migration of brown trout in a small Norwegian river studied by telemetry

The movement of 34 large (39–73 cm standard length) brown trout Salmo trutta was monitored using radio telemetry for up to 74 days in Brumunda, a small Norwegian river (mean annual discharge 3·3 m³ s⁻¹) flowing into the large Lake Mjøsa. The maximum range of movement in the river was 20 km. No clear relationships existed between individual movement and water discharge, temperature and barometric pressure. Brown trout migrated at all levels of water discharge. At low discharge (<2 m³ s⁻¹) movements were nocturnal. A weir 5·3 km from the outlet restricted ascending brown trout at low ( c . 6° C), but not at high ( c . 8° C) water temperatures. Spawning occurred in September to October and tagged individuals spent 2–51 days at the spawning sites. Mean migration speed from tagging to when the fish reached the spawning area, and from when they left the spawning areas and reached the lake was 1·0 and 2·3 km day⁻¹, respectively. All tagged brown trout that survived spawning returned to the lake after spawning.     

Influence of environmental conditions on the ovarian cycle and serum chemistry of Cyprinus carpio in the Dal lake, Kashmir (India)

SUMMARY 1. The study presents adaptive and acclimatory changes observed in Cyprinus carpio communis L with respect to ovarian cycle and serum levels of electrolytes, calcium, total proteins and albumin as a consequence of wide temperature and sunshine variation in the natural environment of Dal lake in Srinagar, Kashmir (India).
2. The atmospheric temperatures in Srinagar show well-defined seasonal and diurnal variations. During the period of study, the mean monthly average temperature in summer (June-August) was 24°C whereas in winter (December-February) it fell to 3.6°C. The total hours of sunshine during the winter months were about half of those found in summer.
3. Under local thermal and photo conditions the fish was found to spawn once a year compared to biannual spawning in tropical chmates.
4. A significant decrease was found in serum sodium, potassium and chloride concentrations during the months of January and February when the mean minimum atmospheric temperatures reached −2.5°C and −l.2°C respectively.
5. The serum calcium levels showed a marked increase during the period corresponding to ovarian maturity and spawning of fish.
6. A significant rise in total serum protein concentration was induced by decreased environmental temperatures. Serum albumin levels were found to exhibit a sharp fall coinciding with the spawning period.     

Effect of water temperature and size of females on the timing of spawning of perch Perca fluviatilis L. in Lake Geneva from 1984 to 2003

The effects of water temperature on the timing of spawning of perch Perca fluviatilis in Lake Geneva were assessed in a 20 year survey (1984–2003). Spawning started at the end of April or at the beginning of May, when the water temperature rose to >10° C, but most of the spawns were laid when water temperature exceeded 12° C. This led to a positive correlation between the date of the mid-spawning period and the date when the water temperature rose to >12° C. Large perch had a tendency to spawn later than the small ones, which led to a positive correlation between the date of mid-spawning period and the yearly mean width of perch egg-ribbons. The coefficient of multiple determination between the date of mid-spawning period and the mean width of the ribbon of spawn, combined with the date when the water temperature rose to >12° C was r ²= 0·77. The perch generally chose deeper spawning places (12 m) at the end of the spawning period than at the beginning (4 m), which was related to water temperature.     

Thermal effects on growth and time to starvation during the yolk-sac larval period of Atlantic mackerel Scomber scombrus L.

The effect of incubation temperature (8·6, 11·1, 13·2, 15·1 and 16·8° C) on north-east Atlantic mackerel Scomber scombrus development, growth and age at starvation during the yolk-sac larval period was investigated. Standard length at hatch was found to be inversely proportional to incubation temperatures within the natural thermal ranges of this species; it ranged from 3·76 mm at 11·1° C to 3·30 mm at 17·8° C. Following hatch, however, larval growth rate was positively related to temperature. Individual logistic models, as a function of temperature and age, were fitted to the development processes of gape, eye pigmentation, jaw mobility and yolk exhaustion. Thereafter, development was classified into different ordered stages and an extended continuation model was fitted to the multinomial ordered stage classification. In all cases, there was a difference of >23 h between the first and the last individual developing in certain stage. The probability of survival decreased with age and was inversely related to temperature. Yolk utilization varied from 4·5 to 8·6 days and individuals died between 7·9 and 12·2 days from 17·8 to 11·1° C. The study demonstrated the significant impact that temperature has on development, growth and survival rates, during the early life history.     

Consequences of elevated temperatures on life-history traits of an introduced fish, pumpkinseed Lepomis gibbosus

Life-history reactions of a pumpkinseed Lepomis gibbosus population in north-eastern France exposed to heated waters were studied. The study was conducted from 2001 to 2003 in an artificial reservoir, adjacent to a nuclear power plant, in which water temperatures are cool in winter (8·2–12·4° C) and rise early in spring (April: 14·7° C) nearly 5° C and 3° C over the temperature of its tributary, respectively. Fast growth among young-of-the-year, precocious maturity and short life span were observed, in contrast to related studies. The short life span appeared to be the price paid for early maturity in breeding fish, which suffered high mortality rates just after their first reproduction.     

Reproduction of Micropogonias funieri in a shallow temperate coastal lagoon in the southern Atlantic

The white croaker Micropogonias furnieri , in the coastal Rocha Lagoon, spawned during 5 months, in late spring and summer. It was eurythermic (gonad growth at 12·5 to 25·5° C, spawning at 20 to 27° C) and mesoxic (living at 5·2 to 9·1 mg l^-1). The spawning occurred in brackish (8–18 salinity), basic ( c . 8 pH) and oxygenated ( c . 8·0 mg l^-1) waters. The temperature appeared to be an important environmental factor affecting the timing of reproduction. The size at first maturity (19–20 cm) was 11–12 cm lower than the reported for the Río de la Plata spawning area (Uruguay). Juveniles were observed throughout most of the year suggesting that the lagoon is also a nursery area. In Brazil, M. furnieri spawns in marine areas while in Uruguay it spawns in estuaries. This is the first time that a coastal lagoon of the subtropical and temperate western coast of the South Atlantic Ocean has been shown to be a spawning area of a marine species.     

Plasma cortisol and 17β-oestradiol levels in roach exposed to acute and chronic stress

Plasma cortisol levels were measured as an indicator of physiological stress in roach subjected to brief handling, or to a 14-day period of confinement, and in undisturbed control fish, during winter (water temperature 5° C) and summer (16° C), at which time plasma 17 β-oestradiol levels were also determined. Cortisol levels in undisturbed roach were low (mean 8·1 ng ml⁻¹ at 5° C; 1·4 ng ml⁻¹ at 16° C) and both handling and handling+confinement elevated blood cortisol levels significantly to 400 and 140 ng ml⁻¹, respectively (at 5° C) and 700 and 600 ng ml⁻¹, respectively (at 16) C). Blood cortisol levels had almost returned to baseline within 4 h following handling alone but in fish subjected to handling and prolonged confinement cortisol levels remained elevated for up to 168 h. Differences in baseline and poststress levels of cortisol, and in the rate of recovery from acute stress, were observed at the two different temperatures and the possible factors underlying these differences are discussed. Circulating levels of 17 β-oestradiol were reduced significantly within 24 h of exposure to either acute handling or chronic confinement indicating that the reproductive endocrine system in roach is sensitive to disruption by stressors.     

Ontogenetic changes in temperature preference of Atlantic cod

Final thermal preferendum ( T ) experiments were conducted in a horizontal thermal gradient tank from the beginning of August 2001 to mid‐November 2001 using Atlantic cod Gadus morhua from 6·5 to 79·0 cm fork length ( L _F). The value of T varied significantly ( P  < 0·005) with L _F( T  = 7·23–0·054 L _F), with smaller (younger) fish choosing higher temperatures than larger (older) fish. The preferendum varied from 6·9° C for fish of 6·5 cm to 3·0° C for those of 79·0 cm. Experiments comparing fish positions in the gradient tank between thermal gradients of 0·5–11·0 and 4·5–14·5° C demonstrated that fish positions were determined by temperature selection instead of undesirable tank effects. This study is the first to demonstrate the effect of ontogeny on temperature preferences of a marine fish species.     

The influence of thermal parameters on the acclimation responses of pinfish Lagodon rhomboides exposed to static and decreasing low temperatures

Pinfish Lagodon rhomboides acclimation rates were determined by modelling changes in critical thermal minimum ( T _{crit min}, ° C) estimates at set intervals following a temperature decrease of 3–4° C. The results showed that pinfish gained a total of 3·7° C of cold tolerance over a range of acclimation temperatures ( T _acc, ° C) from (23–12° C), that cold tolerance increased with exposure time to the reduced temperature at all T _acc, but that the rate of cold tolerance accruement (mean 0·14° C day⁻¹) was independent of T _acc. A highly significant ( P < 0·001) multivariate predictive model was generated that described the acclimation rates and thermal tolerance of pinfish exposed to reduction in water temperature: log₁₀ T _{crit min}= 0·41597 − 0·01704 T _acc+ 0·04320 T _plunge− 0·08376[log₁₀ ( t + 1)], where T _plunge is plunge temperature (° C) and t is the time (days). A comparison of the present data, with acclimation rate data for other species, suggests that factors such as latitude or geographic range may play a more important role than ambient temperature in determining cold acclimation rates in fishes.     

Lack of metabolic thermal compensation during the early life stages of ocean pout Zoarces americanus (Bloch & Schneider) : a benthic, cold-water marine species

The present study investigated the metabolic response of young ocean pout Zoarces americanus to temperature acclimation (3 v. 11° C), and to acute changes in water temperature from 3 to 17° C. The Q ₁₀ value for standard metabolic rate between acclimation temperatures was 5·3, warm-acclimated fish displayed higher rates of oxygen uptake at all temperatures during the acute thermal challenge, and changes in whole-body citrate synthase activity were qualitatively similar to those seen for metabolism. These results indicate that, in contrast to temperate species, young ocean pout from Newfoundland do not show thermal compensation in response to long-term temperature changes.     

Effects of temperature on prey consumption and growth in mass of juvenile trahira Hoplias aff. malabaricus (Bloch, 1794)

The influence of temperature on prey consumption and growth in mass of juvenile trahira Hoplias aff. malabaricus were investigated. Consumption of small-sized lambari Astyanax altiparanae (mean standard length, L _S, 5·43 cm) varied from zero to 65 over a period of 30 days. Temperatures ranged from 14 to 34° C and the size of trahiras ranged from 17·5 to 24·7 cm L _S. Prey consumption differed significantly among temperatures. Trahiras at 18° C consumed significantly less than those at 30° C. A linear multiple regression model including temperature, prey consumption and L _S explained 89·4% of the variability in growth in mass. Some caution is suggested when inferring the impact of H. aff. malabaricus piscivory on assemblage structures in systems that, despite their location in tropical regions, are subjected to seasonal thermal variations.     

Effects of different photoperiods on the reproduction of the barbel, Barbus barbus (L.), reared at constant temperature

The role of photoperiod as an environmental factor controlling reproduction, particularly the duration and ending of the breeding season, in the barbel was investigated by tank experiments. The experiments used a population of barbel matured in captivity which were stripped of eggs at frequent intervals: 10–15 'spawnings'for each female were obtained at 15-day intervals.
A decreasing photoperiod (16·5 light: 7·5 dark→8L: 16D), for an annual cycle contracted to 6 months duration, inhibited the spawning of both female and male fish. This allowed two periods of reproduction (February-May and September-November) within one year. Under natural or constant (10L: 14D) photoperiod conditions, spawning came to an end spontaneously. The rate (accelerated, slow or natural) of daylength increase did not affect the onset of spawning.