Infection by the cestode parasite Schistocephalus sp. and effects on diet,body condition and survival of sculpins Cottus aleuticus and Cottus cognatus

Sampling in Iliamna Lake, Alaska, U.S.A. revealed that a greater proportion of coastrange sculpins Cottus aleuticus were infected by the cestode Schistocephalus solidus than slimy sculpins Cottus cognatus (52 v. 23%), and infected C. aleuticus contained more cestodes than did C. cognatus (2·1 v. 1·3 per fish). Consumption of sockeye salmon Oncorhynchus nerka eggs (the primary diet item) was lower in fishes with cestodes, and a model based on cestode prevalence and age composition estimated higher rates of infection and parasite‐associated mortality in C. aleuticus compared with C. cognatus.     

Reproductive potential of Schistocephalus solidus‐infected male three‐spined stickleback Gasterosteus aculeatus from two U.K. populations

Male three‐spined stickleback Gasterosteus aculeatus from two U.K. populations with endemic infections of the cestode Schistocephalus solidus were brought into the laboratory prior to the breeding season and transferred to nesting tanks under conditions designed to stimulate sexual maturation. Nesting and courtship behaviours were scored over a 35 day period, after which fish were euthanized and the liver, spleen, kidney and gonads were weighed. Among G. aculeatus from a park pond in Leicester, U.K., infected males rarely engaged in reproductive behaviours and exhibited reduced indices of sexual development, body condition and general health, with effects being largely independent of relative parasite mass (parasite index, I_P). In contrast, the reproductive behaviour of infected fish from Kendoon Loch in Dumfriesshire, U.K. appeared to be less severely affected, with infected fish regularly building nests and courting females under laboratory conditions. This was paralleled by a more limited effect of infection on physiological indicators of development, condition and general health. Furthermore, behavioural and physiological variables typically correlated with I_P among infected fish from this population. Although comparing the performance of infected fish from the two populations directly was difficult due to potentially confounding factors, the results support the findings of recent studies showing that the effects of S. solidus on host reproduction are unlikely to be uniform across G. aculeatus populations. One possibility is that variation in the effects of infection arises from differences in the co‐evolutionary association times of G. aculeatus with the parasite.     

The effect of Schistocephalus solidus infection on meal size of three‐spined stickleback

The effect of infection with the pseudophyllidean cestode Schistocephalus solidus on the meal size of individually housed three‐spined stickleback Gasterosteus aculeatus was quantified. Infected fish harboured plerocercoid loads that contributed from 1·1 to 33·9% of their total mass. Across this range of infection levels, the presence of S. solidus infection had no significant directional effect on standard length ( L _S) corrected meal size of host three‐spined sticklebacks. Amongst multiply infected fish there was a significant negative relationship between L _S‐corrected meal size and the proportion of host mass contributed by S. solidus parasites. This relationship, however, did not hold for singly‐infected fish. Furthermore, the data suggest that multiply‐infected fish that harbour a combined mass of parasites contributing < c . 15% to host body mass might exhibit meal sizes that exceed those of length‐matched uninfected fish. The results suggest that although heavy infections can significantly reduce the meal size of heavily infected three‐spined sticklebacks, in the early stages of multiple S. solidus infections host food intake may increase. The probable causes of these differential effects on meal size and their consequences for the host‐parasite system are discussed.     

Body condition and reproductive capacity of three‐spined stickleback infected with the cestode Schistocephalus solidus

The relationship between reproductive ability and the residual index of body condition in three‐spined stickleback Gasterosteus aculeatus from a population infected with the cestode macroparasite Schistocephalus solidus in Walby Lake, Alaska, was examined. In general, reproductive activities resulted in significantly lower levels of body condition in three‐spined stickleback during the latter part of the breeding season, and relatively high levels of S. solidus infection intensified the energetic drain. Although female body condition did not differ significantly due just to the presence of S. solidus , increased parasite index did have a significant negative effect on female body condition. Males showed significantly lower levels of body condition in response to S. solidus infection alone and in association with a greater parasite index. Males had greater mean parasite indices than females. Females had significantly lower body condition than males, which may be due to discrepancies in energy expenditure between the sexes during reproduction. Females with greater body condition were significantly more likely to produce a clutch of eggs than those with lower condition, suggesting a threshold effect of body condition on reproductive capacity.     

Fecundity compensation in the three‐spined stickleback Gasterosteus aculeatus infected by the diphyllobothriidean cestode Schistocephalus solidus

Causal explanations for host reproductive phenotypes influenced by parasitism fit into three broad evolutionary models: (1) non‐adaptive side effect; (2) adaptive parasitic manipulation; and (3) adaptive host defence. This study demonstrates fecundity compensation, an adaptive non‐immunological host defence, in the three‐spined stickleback fish (Gasterosteus aculeatus) infected by the diphyllobothriidean cestode Schistocephalus solidus. Both infected and uninfected female sticklebacks produced egg clutches at the same age and size. The reproductive capacity of infected females decreased rapidly with increased parasite : host body mass ratio. Body condition was lower in infected females than uninfected females and decreased with increasing parasite : host mass ratio. Females with clutches had greater body condition than those without clutches. A point biserial correlation showed that there was a body condition threshold necessary for clutch production to occur. Host females apparently had the capacity to produce egg clutches until the prolonged effects of nutrient theft by the parasite and the drain on resources from reproduction precluded clutch formation. Clutch mass, adjusted for female body mass, did not differ significantly between infected and uninfected females. Infected females apparently maintained the same level of reproductive allotment (egg mass as proportion of body mass) as uninfected females. Infected females produced larger clutches of smaller eggs than uninfected females, revealing a trade‐off between egg mass and egg number, consistent with the fecundity compensation hypothesis. The rapid loss of reproductive capacity with severity of infection probably reflects the influence of the parasite combined with a trade‐off between current and future reproduction in the host. Inter‐annual differences in reproductive performance may have reflected ecological influences on host pathology and/or intra‐annual seasonal changes. © 2012 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, ?? , ??–??.     

Some (worms) like it hot: fish parasites grow faster in warmer water,and alter host thermal preferences

Elevated environmental temperatures associated with anthropogenic warming have the potential to impact host‐parasite interactions, with consequences for population health and ecosystem functioning. One way that elevated temperatures might influence parasite prevalence and intensity is by increasing life cycle completion rates. Here, we investigate how elevated temperatures impact a critical phase of the life cycle of the bird tapeworm Schistocephalus solidus – the growth of plerocercoid larvae in host fish (three‐spined sticklebacks Gasterosteus aculeatus). By 8 weeks post‐infection, plerocercoids recovered from experimentally infected sticklebacks held at 20 °C weighed on average 104.9 mg, with all exceeding 50 mg, the mass considered consistently infective to definitive hosts. In contrast, plerocercoids from sticklebacks held at 15 °C weighed on average 26.5 mg, with none exceeding 50 mg. As small increases in plerocercoid mass affect adult fecundity disproportionately in this species, enhanced plerocercoid growth at higher temperatures predicts dramatically increased output of infective parasite stages. Subsequent screening of thermal preferences of sticklebacks from a population with endemic S. solidus infection demonstrated that fish harbouring infective plerocercoids show significant preferences for warmer temperatures. Our results therefore indicate that parasite transmission might be affected in at least two ways under anthropogenic warming; by enhancing rates of parasite growth and development, and by increasing the likelihood of hosts being able to seek out proliferating warmer microhabitats. Furthermore, our results suggest the potential for positive feedback between parasite growth and host thermal preferences, which could dramatically increase the effects of even small temperature increases. We discuss the possible mechanisms underpinning our results, their likely ecological consequences and highlight key areas for further research.     

A non-invasive morphometric technique for estimating cestode plerocercoid burden in small freshwater fish

A non-invasive morphometric technique is presented which can be used to predict the infection status and the proportion of infected fish weight contributed by parasite tissue in three-spined sticklebacks Gasterosteus aculeatus infected with plerocercoids of Schistocephalus solidus (Cestoda: Pseudophyllidea)     

Introduced bullheads Cottus gobio and infection with plerocercoids of Schistocephalus cotti in the Utsjoki, an Arctic river in Finland

Bullheads Cottus gobio, first found in the River Utsjoki, an Arctic river in Finland, in 1979, were sampled at six sites in August 1991 (two of these sites were also sampled previously in June and July 1991). Mean total length (L_T) of C. gobio was 45 mm (n= 1080 fish). Overall, there were slightly more females than males, with males larger than females (mean L_T males 52·1 and females 47·6 mm). Prevalence of infection with plerocercoids of Schistocephalus cotti varied from 20·0 to 43·0% over the six sites in August. Juvenile C. gobio had a prevalence of infection of 3·5% whereas in mature fish prevalence was consistently higher in females than in males (38·8 v. 20·1%). There was one plerocercoid per infected juvenile C. gobio. In mature fish the mean number varied between 1·3 and 1·8: 49% had one worm per fish, 38% two or three worms and 13% had four to eight plerocercoids. In juvenile C. gobio, S. cotti were randomly distributed (overdispersion index 1·10), whereas occurrence was slightly aggregated in the L_T groups 40–59 and ≥60 mm (overdispersion indices both 1·90). Mean mass of infected fish was higher in all L_T groups compared to uninfected C. gobio. After removal of plerocercoids, mean mass of fish tissue remaining was lower compared with uninfected fish for the two L_T groups 40–59 and ≥ 60 mm, but higher in C. gobio <40 mm L_T. Prevalence and mean intensity of infection over the 3 months did not differ either for the two sites individually or the pooled data. Mean mass of both uninfected and infected fish increased over this period, and were both highest in August as was the mean worm burden. There was, however, no difference in Fulton’s condition factor at any time. Mean mass of plerocercoids in C. gobio of ≥40 mm L_T increased significantly comparing June and July with August. Comparison of backcalculated L_T of infected and non‐infected bullheads of different age‐groups did not show any significant differences in growth at any age. In each parasite infrapopulation as the number of worms increased so their mean mass decreased significantly but at the same time the total mass of worms in the fish host remained more or less constant in relation to length. Aggregation of parasites in the fish population was low, as the majority were infected by one S. cotti plerocercoid. Gonad development was suppressed in infected C. gobio.     

Consequences of divergent temperature optima in a host–parasite system

It was suggested that parasite infections become more severe with rising temperature, as expected during global warming. In ectothermic systems, the growth of a parasite and therefore its reproductive capacity is expected to increase with temperature. However, the outcome of the interaction depends on the temperature optima of both host and parasite. Here we used experimental infections of three‐spined stickleback fish Gasterosteus aculeatus with its specific tapeworm parasite Schistocephalus solidus to investigate in detail the temperature optima for both host and parasite. We analyzed the fitness consequences thereof, focusing on growth and immunity of the host, and growth and offspring production of the parasite as fitness correlates. We checked for potential differences among populations, using the offspring of hosts and parasites derived from four study sites in Iceland, Germany and Spain that differ in average annual temperature ranging between 4.8°C and 18.4°C. We found differences in temperature optima of host and parasites that were quite consistent across the populations: while sticklebacks grew faster and had higher immune activity at low temperatures, the parasites did not even grow fast enough to reach sexual maturity in these conditions. By contrast, with increasing temperatures, parasite growth, egg production and offspring hatching increased strongly while host immunity and growth were impaired. Our results show that divergent temperature optima of hosts and parasites can have drastic fitness consequences and support the expectation that some parasites will benefit from global warming.     

Effects of fasting and feeding on the fast‐start swimming performance of southern catfish Silurus meridionalis

This study investigated the effects of fasting and feeding on the fast‐start escape swimming performance of juvenile southern catfish Silurus meridionalis, a sit‐and‐wait forager that encounters extreme fasting and famine frequently during its lifespan. Ten to 30 days of fasting resulted in no significant change in most of the variables measured in the fast‐start response except a 20–30% decrease in the escape distance during the first 120 ms (D_120ms) relative to the control group (48 h after feeding). The ratio of the single‐bend (SB) response (lower energetic expenditure) to the double‐bend (DB) response increased significantly from 0% in the control group to 75 and 82·5% in the 20 and 30 day fasting groups, respectively. Satiated feeding (25% of body mass) resulted in a significantly lower (36·6%) maximum linear velocity (V_max) and a significantly lower (43·3%) D_120ms than in non‐fed fish (control group, 48 h after feeding). Half‐satiated feeding (12·5% of body mass), however, showed no significant effects on any of the measured variables of the fast‐start response relative to control fish. It is suggested that the increase in the ratio of SB:DB responses with fasting in S. meridionalis may reflect a trade‐off between energy conservation and maintaining high V_max, while variables of fast‐start performance were more sensitive to feeding than fasting might be an adaptive strategy to their foraging mode and food availability in their habitat.     

A three‐phase excess post‐exercise oxygen consumption in Atlantic salmon Salmo salar and its response to exercise training

The recovery of oxygen uptake to the standard metabolic rate (SMR) following exhaustive chasing exercise in Atlantic salmon Salmo salar parr occurred in three phases (rapid, plateau and slow). The initial recovery phase lasted 0·7 h and contributed 16% to the total excess post‐exercise oxygen consumption (EPOC). It was followed by a longer plateau phase that contributed 53% to the total EPOC. The slow recovery phase that completed recovery of SMR, which has not been reported previously, made a 31% contribution to the total EPOC. The plasticity of EPOC was demonstrated in exercise‐trained fish. Exercise training increased EPOC by 39% when compared with control fish (mean ± S.E., 877·7 ± 73·1 v . 629·2 ± 53·4 mg O₂ kg^?1, d.f. = 9, P <  0·05), with the duration of the plateau phase increasing by 38% (4·7 ± 0·58 v . 3·4 ± 0·16 h, d.f. = 9, P <  0·05) and the contribution of the slow phase to the total EPOC increasing by 80% (173·9 ± 23·9 v . 312·5 ± 50·4 mg O₂ kg^?1, d.f. = 9, P  < 0·05). As a result, the combination of the plateau and slow phases of exercise‐trained fish increased by 47% compared with control fish (756·6 ± 71·4 v . 513·6 ± 43·1 mg O₂ kg^?1; d.f. = 9, P  = 0·01). To substantiate the hypothesis that the plateau and slow recovery phase of EPOC was related to general metabolic recovery following exhaustive exercise, the time‐course for recovery of SMR was compared with previously published metabolite recovery profiles. The final phase of metabolic recovery was temporally associated with the final phases of gluconeogenesis, lactate oxidation and muscle intracellular pH regulation. Therefore, the plasticity of the latter phase of EPOC agreed with the known effects of exercise training in fishes.     

Comparison of the prolonged swimming performances of closely related, morphologically distinct three‐spined sticklebacks Gasterosteus spp.

Prolonged swimming performances of two as yet unnamed species of three‐spined stickleback, Gasterosteus spp., were compared. The two fishes (not yet formally described, referred to here as benthic and limnetic) inhabit different niches within Paxton Lake, Texada Island, British Columbia, Canada, and are recent, morphologically distinct species. Limnetics had longer endurance during prolonged swimming than did benthics. The mean regression of the log₁₀ of fatigue time (F_t, s) on swimming speed (U, standard length, L_S s^?1) for limnetics (log₁₀F_t = 7·03 ? 0·46U) had a similar slope, but a significantly higher intercept than that for benthics (log₁₀F_t = 5·55 ? 0·43U). Adult benthics were larger, heavier and deeper‐bodied fish than limnetics. Limnetics, however, had a significantly greater pectoral fin edge:base ratio (mean ± s .e .: limnetics, 4·58 ± 0·43; benthics, 3·63 ± 0·27). In addition, limnetics had significantly lower drag coefficients (C_D) than benthics (limnetics, log₁₀C_D = ?0·49log₁₀R_e + 0·66; benthics, log₁₀C_D = ?0·26log₁₀R_e ? 0·30) where R_e is the Reynolds number [(L_SU (ν^?1), where U and ν are swimming velocity and the kinematic viscosity of the water, respectively]. Compared to their ancestral form, the anadromous three‐spined stickleback Gasterosteus aculeatus L., limnetics and benthics had significantly longer and shorter endurance times, respectively. In addition, both these fishes had significantly higher fast‐start velocities than their ancestral form. Selection due to differential resource use may have lead to divergence of body form, and, therefore, of steady swimming performance. Therefore predation may be the selective force for the similar high escape performance in these two fishes.     

Evolutionary significance of fecundity reduction in threespine stickleback infected by the diphyllobothriidean cestode Schistocephalus solidus

Parasites may cause fecundity reduction in their hosts via life‐history strategies involving simple nutrient theft or manipulation of host energy allocation. Simple theft of nutrients incidentally reduces host energy allocation to reproduction, whereas manipulation is a parasite‐driven diversion of energy away from host reproduction. We aimed to determine whether the diphyllobothriidean cestode parasite Schistocephalus solidus causes loss of fecundity in the threespine stickleback fish (Gasterosteus aculeatus) through simple nutrient theft or the manipulation of host energy allocation. In one stickleback population (Walby Lake, Matanuska‐Susitna Valley, Alaska), there was no difference in the sizes and ages of infected and uninfected reproducing females. Lightly‐ and heavily‐infected females produced clutches of eggs, but increasingly smaller percentages of infected females produced clutches as the parasite‐to‐host biomass ratio (PI) increased. Infected, clutch‐bearing sticklebacks showed reductions in clutch size, egg mass, and clutch mass, which were related to increases in PI and reflected a reduction in reproductive parameters as growth in parasite mass occurs. The findings obtained for this population are consistent with the hypothesis of simple nutrient theft; however, populations of S. solidus in other regions may manipulate host energy allocation. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 100 , 835–846.     

Myotube production in fast myotomal muscle is switched-off at shorter body lengths in male than female Atlantic halibut Hippoglossus hippoglossus (L.) resulting in a lower final fibre number

A sampling method is described to determine accurately the number of fast myotomal muscle fibres (N_F) in a large flatfish species, the Atlantic halibut Hippoglossus hippoglossus. An unusual feature of the fast myotomal muscle is the presence of internalized strips of slow muscle fibres. In fish of 1·5–3·5 kg (n = 24), the total cross‐sectional area (A_TC) of fast muscle was 18% greater in the dorsal than ventral myotomal compartments (P < 0·05), whereas there was no significant difference between left‐ and right‐hand sides of the body. Due the bilateral asymmetry, muscle blocks (5 × 5 × 5 mm) were prepared to systematically sample each myotomal quadrant (dorsal, ventral, left‐ and right‐side) and the diameters of 150 fast fibres measured per block. Smooth non‐parametric probability functions were fitted to a minimum of 800 measurements of fibre diameter per quadrant (n = 5). There were no significant differences in the distribution of muscle fibre diameters between myotomal compartments and therefore N_F could be estimated from a single quadrant. The number of blocks required to estimate N_F with a repeatability of ±2·5% increased from six at 300 g body mass to 17 at 96·5 kg, caused by variation within and between blocks. Gompertz curves were fitted to measurements of fibre number and fork length (L_F). The estimated final fibre number was 8·96 × 10⁵ (7·99–9·94 × 10⁵, 95% CI) for males and 1·73 × 10⁶ (1·56–1·90 × 10⁶, 95% CI) for female fish. The estimated L_F for cessation of fibre recruitment in the fast muscle of female fish (1775 mm) was almost twice that in males (810 mm), reflecting their greater ultimate body size.     

Effects of administration of somatostatin-14 and immunoneutralization of somatostatin on endocrine and growth responses in rainbow trout

Injection of somatostatin‐14 (SS‐14) at 5 ng g^?1 body mass (BM) into rainbow trout Oncorhynchus mykiss decreased (P < 0·05, cubic, r² = 0·54) levels of growth hormone (GH) (1·5 ± 0·9 ng ml^?1v. 6·6 ± 0·6 ng ml^?1) over time when compared to controls. Somatostatin‐14 at 50 ng g^?1 BM also decreased (P = 0·064, quadratic; r² = 0·30) levels of GH (3·6 ± 2·1 ng ml^?1v. 6·6 ± 0·6 ng ml^?1) over time compared to controls. In a second study, passive immunization against SS‐14 (1 : 25 dose) increased (P = 0·10, cubic, r² = 0·12) levels of GH (11·0 ± 4·8 ng ml^?1v. 5·2 ± 1·4 ng ml^?1) over time. Passively immunizing against SS‐14 (1 : 50 dose) increased (P < 0·05, cubic, r² = 0·10) levels of GH (8·2 ± 2·3 ng ml^?1v. 5·2 ± 1·4 ng ml^?1) over time compared to controls. Overall, in the active immunization study there was no difference (P > 0·10) in specific growth rate (G) or feed conversion ratio (FCR) between the three treatment groups during the 9 weeks of the study. Only four of the fish immunized against SS‐14, however, developed antibody titres against SS. Compared to controls, these fish exhibited a G of 0·89 ± 0·09 v. 0·56 ± 0·09% per 3 weeks and FCR of 0·80 ± 0·04 v. 1·20 ± 0·05 g g^?1. In SS‐14 immunized fish, levels of GH decreased (P < 0·05) by day 63 while levels of insulin like growth factor‐I (IGF‐I) increased (P < 0·05) by day 42 and 63. These results indicate the hypothalamic hormone SS‐14 regulates GH secretion similarly in rainbow trout as it does in mammals. Active immunization against SS‐14 could improve growth performance in rainbow trout but enhanced G and FCR is dependent upon generation of antibody titres.     

Transmission of neozoic Anguillicoloides crassus and established Camallanus lacustris in ruffe Gymnocephalus cernuus

In the present study, groups of ruffe Gymnocephalus cernuus, reared singly, were exposed to defined numbers of Anguillicoloides crassus or Camallanus lacustris under controlled laboratory conditions. Infection took place orally through feeding G. cernuus with axenically cultured and laboratory infected copepods, in which the parasites had developed to the infective third stage (L3). Mean prevalence (94·3%) and infection probability (38·5%) for the established C. lacustris were significantly higher than for the neozoic A. crassus (14·3 and 1·0%, respectively). Peripheral blood leukocytes were significantly increased in infected fish, apparently independent of exposure level, parasite species or intensity of infection compared to the controls. In infected fish, the gonado‐somatic index (I_G) was significantly reduced by c. 50%, and the spleen‐somatic index (I_S) was significantly increased compared to controls. Both parasites raised similar physiological and immunological responses in G. cernuus, which was able to effectively reject the neozoic A. crassus.     

Spatial ecology of coastal Atlantic cod Gadus morhua associated with parasite load

Acoustic tags and receivers were used to investigate the spatial ecology of coastal Atlantic cod Gadus morhua (n = 32, mean fork length: 50 cm, range: 33–80 cm) on the Norwegian Skagerrak coast in 2012. Monthly home ranges (HR), swimming activity and depth use varied considerably among individuals and through the months of June, July and August. HR sizes for the period ranged from 0·25 to 5·20 km² (mean = 2·30 km²). Two thirds of the tagged G. morhua were infected with black spot disease Cryptocotyle lingua parasites; these fish had larger HRs and occupied deeper water compared with non‐infected fish. The infected fish also tended to be more active in terms of horizontal swimming. From an ecological and evolutionary perspective, any environmental change that modifies G. morhua behaviour may therefore also alter the parasite load of the population, and its conservation and fishery status.     

Physical training prevents oxidative stress in L‐NAME‐induced hypertension rats

The present study investigated the effects of a 6‐week swimming training on blood pressure, nitric oxide (NO) levels and oxidative stress parameters such as protein and lipid oxidation, antioxidant enzyme activity and endogenous non‐enzymatic antioxidant content in kidney and circulating fluids, as well as on serum biochemical parameters (cholesterol, triglycerides, urea and creatinine) from Nω‐nitro‐L‐arginine methyl ester hydrochloride (L‐NAME)‐induced hypertension treated rats. Animals were divided into four groups (n = 10): Control, Exercise, L‐NAME and Exercise L‐NAME. Results showed that exercise prevented a decrease in NO levels in hypertensive rats (P < 0·05). An increase in protein and lipid oxidation observed in the L‐NAME‐treated group was reverted by physical training in serum from the Exercise L‐NAME group (P < 0·05). A decrease in the catalase (CAT) and superoxide dismutase (SOD) activities in the L‐NAME group was observed when compared with normotensive groups (P < 0·05). In kidney, exercise significantly augmented the CAT and SOD activities in the Exercise L‐NAME group when compared with the L‐NAME group (P < 0·05). There was a decrease in the non‐protein thiols (NPSH) levels in the L‐NAME‐treated group when compared with the normotensive groups (P < 0·05). In the Exercise L‐NAME group, there was an increase in NPSH levels when compared with the L‐NAME group (P < 0·05). The elevation in serum cholesterol, triglycerides, urea and creatinine levels observed in the L‐NAME group were reverted to levels close to normal by exercise in the Exercise L‐NAME group (P < 0·05). Exercise training had hypotensive effect, reducing blood pressure in the Exercise L‐NAME group (P < 0·05). These findings suggest that physical training could have a protector effect against oxidative damage and renal injury caused by hypertension. Copyright © 2012 John Wiley & Sons, Ltd.     

Growth, sex differentiation and gonad and plasma levels of sex steroids in male‐ and female‐dominant populations of Dicentrarchus labrax obtained through repeated size grading

Starting from 66 days post hatching (dph), European sea bass Dicentrarchus labrax were graded successively to create a fast growing (L‐extreme) and a slow growing (S‐extreme) population. The L‐extreme population grew significantly larger (ANOVA, n = 89–101, P < 0·01) attaining twice the wet mass of the S‐extreme population at 300 dph (130·9 ± 1·8 v. 66·7 ± 0·9 g, mean ± s .e .). When the two populations were sexed, the L‐extreme consisted of 96·5% and the S‐extreme of 30·2% females, while the ungraded control had 59·2% females. Sex differentiation began first in females at a total length (L_T) of 97 ± 4 mm and wet mass of 9·4 ± 1·2 g (150 dph), and was completed when fish reached 166 ± 6 mm and 53·4 ± 6·4 g (250 dph) in both sexes. Precocious maturation in males was positively correlated to growth. Gonad oestradiol (E₂) was significantly higher in the female‐dominant population at the onset of ovarian differentiation (ANOVA, n = 10, P < 0·05) and in the plasma after the appearance of the first primary oocytes (P < 0·01). Gonad testosterone (T) increased in both populations after sex differentiation (ANOVA, n = 10, P < 0·05), while plasma levels were significantly higher in the male‐dominant population (P < 0·001). Both gonad and plasma 11‐keto testosterone (11‐KT) were significantly higher in the male‐dominant population (ANOVA, n = 10, P < 0·01) reaching maximal values at spermiation. The results suggest that E₂ is closely related with ovarian differentiation and the onset of oogenesis, while T and 11‐KT is more related to spermatogenesis and precocious maturation.