The effects of a prolonged photoperiod and light source on growth,sexual maturation,fin condition,and vulnerability to fungal disease in brook trout Salvelinus fontinalis

The effects of an artificially prolonged photoperiod on growth, survival rate, colouration, and sexual maturation in brook trout Salvelinus fontinalis during pre‐ and post‐spawning periods from 21 June to 06 November were investigated. Fish of mean initial weight ?150 g were reared at ambient photoperiod as well as with an artificially prolonged photoperiod produced by either a light‐emitting diode or a metal‐halide light. The fish groups subjected to a prolonged period of artificial light grew significantly larger and had a higher survival rate (p < 0.05), regardless of sex, and showed lower occurrence of fungal disease compared to controls reared in the natural photoperiod. We found a significantly higher number of sexually mature fish in the control groups compared with experimental groups. The increased photoperiod effectively delayed gonad development and increased somatic growth in both male and female brook trout, and also increased resistance to fungal disease. The increased photoperiod produced an observable difference in fish colouration, with control groups exhibiting more intensive spawning colouration.     

The effect of timing of extended photoperiod on growth and maturity of brook trout (Salvelinus fontinalis)

The influence of timing of extended photoperiods on growth and maturity of brook trout was investigated in a 112‐day experiment. The fish with mean initial weight of ~192 g were reared under four light regimes: one control group with natural ambient photoperiod and three groups exposed to an 18L:6D regime initiated at days 1, 23 or 46 of the growth trial. Light‐emitting diodes, with intensity of 250–1000 lux, depending on the distance from the light source, were used for extending light periods. There was a positive effect of prolonged day length on fish growth (p < 0.05), and a delay in gonad development and sexual maturity. Significantly higher numbers of sexually mature fish were found among controls groups, regardless of sex. Survival rate was not affected by light regime. This study demonstrated that the short‐term expansion of the photo period delayed maturation and increased the growth rate of brook trout.     

Growth in adult gilthead sea bream (Sparus aurata L) as a result of interference in sexual maturation by different photoperiod regimes

Gilthead sea bream (Sparus aurata L) pass through the period of sexual maturation while being intensively reared for commercial purposes. This process affects growth and food conversion efficiency. In an attempt to reduce this problem several lighting regimes have been utilized which impede gonad development by increasing the length of the day. A four hour increase in natural day length three months before reaching sexual maturation in fish of 390 g, improves growth in comparison to the control by about 15% (means SD of 606.2 ± 10.6 and 526.5 ± 12.7 g, respectively) towards the end of the natural reproductive season. However, these differences are subsequently compensated since the sexual maturation process is only delayed (rather than being permanently halted). The manipulated groups reached maturity and then stopped growing between three and four months after the control groups. For this reason, it would appear advantageous to manipulate sexual maturation through photoperiod alteration in those groups which go to market either during or towards the end of the reproductive season since greater fish weights will be achieved in addition to an improved food efficiency.     

Influence of photoperiod and temperature manipulation on gonadal development and spawning in Caspian roach (Rutilus rutilus caspicus): Implications for artificial propagation

Caspian roach (Rutilus rutilus caspicus), a spring spawning teleost, were subjected to various photoperiod and temperature regimes to study the feasibility of shifting the timing of spawning for artificial propagation purposes. A total of 650 female reproductively mature R. rutilus caspicus were subjected to different photoperiod and temperature regimes including four light regimes (natural light (NL), 16 hr of light (L):8 hr of darkness (D), 9L:15D, 11L:13D), each affected by three temperature regimes (14, 20 and 24°C) for 70 days. Five fish per tank were randomly sampled on Feb. 10, Feb. 20, March 28, April 15 and April 30 (natural spawning time). Ovarian tissue sections were studied using light microscope and transmission electron microscope (TEM). The levels of 17‐β estradiol (E2) and 17α‐hydroxyprogesterone (OHP) were also measured in the serum samples. In late winter (March 28th), the gonadal maturation and spawning were accelerated in fish treated with the long day length (16L/8D) and warm temperature (20°C). While, the maturation of oocytes and spawning delayed in fish exposed to low temperature (14°C) and short day length (9L/15D and 11L/13D). Photoperiod seems to play a more important role in the ovarian development of the R. rutilus caspicus compared to temperature; since even among the fish treated with the lowest temperature (14°C), those exposed to a longer day length (16L/8D), matured and spawned earlier than the others. Considering that the earliest spawning occurred in R. rutilus caspicus treated with 16L/8D at 20°C and the latest spawning occurred in fish exposed to low temperature and short photoperiod, it can be concluded that temperature and photoperiod play an important role in accelerating oocyte maturation and spawning.     

Do summer temperatures trigger spring maturation in Pacific lamprey,Entosphenus tridentatus?

Abstract –  Pacific lamprey, Entosphenus tridentatus , return to streams and use somatic energy to fuel maturation. Body size decreases, the lamprey mature, spawn, and then die. We predicted that warm, summer temperatures (>20 °C) would accentuate shrinkage in body size, and expedite sexual maturation and subsequent death. We compared fish reared in the laboratory at diel fluctuating temperatures of 20–24 °C (mean = 21.8 °C) with fish reared at cooler temperatures (13.6 °C). The results confirmed our predictions. Lamprey from the warm water group showed significantly greater proportional decreases in body weight following the summer temperature treatments than fish from the cool water group. A greater proportion of warm water fish sexually matured (100%) and died (97%) the following spring than cool water fish (53% sexually mature, 61% died). Females tended to mature and die earlier than males, most obviously in the warm water group.     

Growth and sexual maturation in Atlantic salmon, Salmon, salar L., reared in sea cages at two different light regimes

Abstract. Immature 1-sea-winter (ISW) Atlantic salmon, Salmo salar L. were reared in sea cages under natural light or constant additional light from 15 October 1987 to 24 June 1988 when the fish were fin clipped according to photoperiod and reared in a common cage under natural photoperiod until maturation. The group subjected to constant additional light (LL) had an overall increase in growth rate, which indicates a seasonal growth pattern influenced by photoperiod. An advanced ovulation time in the LL group gives further support to the hypothesis that endogenous rhythms controlling growth rate have been influenced. Incidence of maturation was lowest in the LL group.     

Growth, feed conversion efficiency and growth heterogeneity in Atlantic halibut (Hippoglossus hippoglossus) reared at three different photoperiods

Juvenile Atlantic halibut, Hippoglossus hippoglossus (initial weight (SD) 191.3 (±44.7)) g, were reared for 99 days at a constant temperature of 11°C and subjected to three different light regimes from 13 September to 21 December: continuous light (LD24:0), simulated natural photoperiod of Bergen (60°25′N, LDN) and constant 20 h light:4 h dark (LD20:4). The fish reared on the different photoperiod regimes differed in their growth patterns as juveniles exposed to long days, i.e. LD20:4 and LD24:0, exhibited faster growth than those experiencing a natural photoperiod. The LD20:4 group showed the highest average specific growth rate (0.72% body weight day^?1), whereas fish on LDN displayed the lowest average specific growth rate (0.60% body weight day^?1). The final mean weights of the LD20:4 and the LD24:0 groups were 15% and 12% higher than those of the LDN group. Dividing the duration of the experiment into three time periods shows that the LD20:4 and LD24:0 had a higher feed conversion efficiency (FCE) as compared with the LDN group during the first and the last period, while a reversed situation was observed in the second period. Our data indicate a larger variation in growth rates among individuals in the best‐performing groups (here LD20:4 and LD24:0). This may indicate that formation of size hierarchies is more pronounced in groups with more homogenous growth (here LDN). Overall, our findings indicate that extended light regimes result in faster growth and better feed conversion in juvenile Atlantic halibut. In line with findings on other flatfish species, this supports the concept that constant long day:short night or continuous light regimes should be used by the farmer in order to maximize growth and improve feed conversion in Atlantic halibut.     

Environmental Manipulation of Growth and Sexual Maturation in Yellow Perch, Perca flavescens

Yellow perch, Perca flavescens, exhibit sexually dimorphic growth detected as the fish enter puberty. The purpose of this study was to evaluate the differential influences of photoperiod and temperature on the sexual maturation and dimorphic growth pattern of yellow perch. Four combinations of constant (CP) or natural (NP) photoperiod with constant (CT) or natural (NT) temperature were evaluated (CPCT, CPNT, NPCT, NPNT). Following 6 months of growth, results indicate that (1) CT is the strongest promoter of overall growth regardless of photoperiod. Perch reared under CT were 26.4 ± 8.1 g heavier than perch reared under NT (P < 0.0001). (2) CP also promotes overall growth regardless of temperature. CP perch outgrew NP perch by 7.0 ± 8.1 g (P < 0.0872). (3) NP (decreasing) initiates maturation in yellow perch regardless of temperature. (4) NT is required for late maturational processes. While both NP groups initiated maturation, only NPNT females were able to recruit oocytes to a vitellogenic stage. Only NPNT males were able to sustain spermiation to the end of the study. (5) CPCT confer the best overall growth performance, fully inhibit maturation in both genders, and suppress a sexually dimorphic growth pattern up to 53 g average weight. These results indicate that using a CPCT regime during intensive fingerling production will produce a larger, more uniform fish population that could alleviate losses as a result of cannibalism. Perch that remained immature did not exhibit a dimorphic growth pattern.     

Interactions of temperature,size and photoperiod on growth and smoltification of chinook salmon (Oncorhynchus tshawytscha)

Underyearling fall chinook salmon (Oncorhynchus tshawytscha) were reared at two temperatures (9 and 15°C) and three photoperiods simulating winter (WIN), spring—summer (SS), and natural (NAT) conditions. The two artificial photoperiods were adjusted according to fish size so that an equinoctial photoperiod was synchronized with a hypothesized optimum size range for smolting (8–14 cm fork length). Fish exposed to a winter (WIN) photoperiod had the slowest growth rate. Fish under the SS photoperiod at both temperatures and under the WIN photoperiod at 9°C displayed hypoosmoregulatory capability near the equinoctial daylength. Thyroxine concentrations in fish reared under a natural photoperiod remained at basal levels during the period of early saltwater adaptiveness and throughout the remainder of the experiment. Thyroxine titers showed significant increases under all experimental photoperiod—temperature combinations near the equinoctial daylength with the exception of the 15°C/SS treatment.     

Effects of photoperiod on growth and spawning efficiency of Nile tilapia (Oreochromis niloticus L.) broodstock in a recycling system

This study was conducted to evaluate the effects of photoperiod on the growth, feed conversion ratio (FCR) and spawning performance of Nile tilapia (Oreochromis niloticus) broodstock. Duplicate groups of two males (66±3.04 g) and six females (50.5±1.58 g) were stocked in 0.4 m³ fibreglass tanks in a recirculating water system at a male:female ratio of 1:3. The fish were subjected to four photoperiod treatments: 24:0 light:dark (L:D), 18L:6D, 12L:12D and 6L:18D. Light intensity was kept constant at about 2500 lx throughout the study. The fish were fed a commercial tilapia diet (35% crude protein and 16.6 MJ GE kg⁻¹) at a daily rate of 2–3% of tank biomass, twice a day, for 130 days. Males grew significantly faster than females under all photoperiod regimes. The best growth rate and FCR were attained at 18L:6D, followed by 24L:0D, 12L:12D and 6L:18D respectively. The number of eggs per female, number of eggs per spawn and number of spawnings per female were all significantly higher in the 12L:12D treatment than in all other photoperiod cycles. Interspawning intervals and days elapsed per spawn were also shorter in the 12L:12D treatment. The time to first spawning was slightly longer in the 24L:0D and 6L:18D than in 12L:12D and 18L:6D light phases. The 18L:6D and 6L:18D photoperiods produced the lowest spawning performance. It is concluded that a 12L:12D photoperiod regime should be adopted for maximum fecundity, seed production and spawning frequencies of Nile tilapia broodstock reared in intensive, recirculating systems. If maximum reproduction is desired, a near‐natural day length photoperiod should be used.     

Natural food and artificial,dry starter diets: effects on growth and survival in intensively reared European grayling

Four artificial, dry feeds and two diets consisting of natural, live food were evaluated for use as starter diets in the intensive rearing of European grayling (Thymallus thymallus). Long-term effects of the different diets were also studied. The investigation was divided into two parts: a 14 day starter period and the subsequent 115 days, during which the long-term effects were studied. Diets differed between the different treatment groups during the initial 2 weeks, whereafter all fish were offered a single diet. At the end of the starter period, significant differences in weight (p<0.001) were obtained between natural (control) feed groups and three of the artificial feed groups. The highest growth rate (9.6% day^–1), and length increase (9 mm) as well as the lowest mortality rate (6.0%) were obtained with one of the artificial diets. Growth rate, length increase and mortality of grayling in the other diet groups varied from 3.6 to 7.7% day^–1, 5 to 7 mm and 7.0 to 9.1%, respectively. The switchover to a different dry diet resulted in an increase in mean daily mortality for all groups previously fed a dry diet. For the fish previously fed live food the mortality rate remained about the same. Groups of fish growing slowly during one period seemed to compensate for their initially low growth by increasing their growth rates during the next period. The highest mean daily mortality for all groups during the experiment was observed during the period with the highest water temperature. It was concluded that European grayling can be intensively reared during the start-feeding phase on artificial as well as natural diets, and that artificial dry diets can be used exclusively throughout the first summer.     

Effects of constant light on haematological parameters of cultured rainbow trout (Oncorhynchus mykiss) in the Southern Hemisphere

The effects of artificial photoperiod regimes on reproductive patterns have been studied in several species, as have haematological parameters. However, information on how artificial photoperiods may affect blood components is scarce, especially under field conditions. We have assessed the effects of constant light [long day (LD) photoperiod: 24 h (light):0 h (dark)] on haematological parameters of cultured rainbow trout in Chile (Southern Hemisphere). In the initial stage (March up to June), two groups of fish were maintained under similar conditions and under the ambient (natural) photoperiod (NP). One group was then placed under the LD photoperiod regime for 2 months (June/July), following which it was returned to␣the NP (August–January); the control group remained under the NP throughout the experiment (March–January). All fish were assessed for haematological parameters and growth performance at various times during the experiment. During the initial stage, no differences were found between groups. However, at the end of the LD 24:0 period, the LD fish had increased haematocrit values and erythrocyte numbers and diminished mean corpuscular haemoglobin. After the LD fish had been returned to the NP, they developed secondary sexual characteristics and had a 40–44% decrease in the number of leukocytes.     

The relation between age at first maturity and growth in Atlantic halibut (Hippoglossus hippoglossus) reared at four different light regimes

The effect of extended photoperiods on growth and age at first maturity was investigated in 166 (79 females and 87 males) individually tagged Atlantic halibut. The halibut were reared at 11°C on four different light regimes from 10 February to 6 July 1996: simulated natural photoperiod, (LDN), continuous light (LD24:0), constant 8 h light and 16 h darkness (LD8:16) and LD8:16 switched to continuous light on 4 May 1996 (LD8:16–24:0). From 6 July 1996 to 9 February 1998 the LD24:0 and LD8:16–24:0 were reared together under continuous light and the LDN and LD8:16 together under natural photoperiod. Juveniles subjected to continuous light exhibited faster growth than those experiencing a natural photoperiod or a constant short day. Moreover, the results suggest an overall growth enhancing effect of continuous light in females, but not in males. No females matured during the trial, but the proportion of mature males differed between the photoperiod groups, with significantly fewer males maturing in groups reared at continuous light. Independent of photoperiod regime and maturation status, females were significantly bigger than males from 14 April 1997 onwards. Immature males were bigger than maturing males from 23 March 1996 onwards. As continuous light reduced maturation at age 2+ in males, this could be used to reduce precocious maturation in males.     

Breeding and larval rearing of the rabbitfish,Siganus guttatus (Bloch)

Females of Siganus guttatus reared to sexual maturity in canvas tanks were induced to spawn by using human chorionic gonadotropin (HCG, Ayerst) at 500 IU/fish or about 2 IU/g body weight. The amount of HCG used depended on the initial mean egg diameter; the smaller the diameter, the more HCG was used. Fish with oocytes characterized by germinal vesicle migration (mean egg diameter ≥ 0.47 mm) spawned without HCG injection. Fertilization and hatching rates for both treated and untreated fish were more than 90%. The larvae were reared to metamorphosis using rotifers from day 2–17, rotifers + newly hatched Artemia nauplii from day 18–20 and rotifers + newly hatched Artemia nauplii + artificial feed from day 21–35. In addition, Isochrysis galbana was introduced to the rearing tanks from day 1–10 and Chlorella sp. and/or Tetraselmis sp. from day 1–35. Survival rates of larvae tended to be lower as the broodstock became older.     

Effects of Lighting Spectrum and Disturbance Level on the Growth and Stress Responses of Yellow Perch Perca flavescens

Abstract.— We evaluated the effects of different lighting spectra and routine disturbances on the growth and stress responses of yellow perch Perca, flavescens. Fish were reared in tanks under one of three different lighting spectra: blue (405–530 nm), red (600–750 nm). or full spectrum (380–750 nm). For each lighting spectrum, fish were reared under one of two disturbance levels: one in which the fish were exposed to 2–4 daily routine disturbances which typify intensive tank culture conditions (e.g., casting shadows over the tank, sham tank siphoning, and dissolved oxygen measurement: ‘disturbed’). or a second treatment in which such disturbances were minimized (‘undisturbed’). The fish were reared for 87 d under temperature, photoperiod. and feeding conditions near optimal for the growth of yellow perch. The cortisol stress response of the different fish groups was evaluated by measuring baseline serum cortisol levels on days 0, 1,3, and 21, and by measuring cortisol levels 30 min after the application of an acute handling stressor on days 0, 1, and 3. Treatment effects on growth were measured from days 21–86 of the study. On day 87, various organs and parameters were evaluated to compare the health and condition of fish reared under the different treatments. Disturbed fish gained less weight and length, and had a significantly lower condition factor than undisturbed fish. Additionally, the disturbed fish showed no signs of acclimation to the frequent disturbances. The fish under red and full spectrum light gained more length than those under blue light. Frequent disturbance had a greater negative effect on length gain in fish reared under red light than in those reared under the other light treatments. On day 21, but not on other days, baseline cortisol levels were higher in disturbed than in undisturbed fish. Undisturbed fish had higher levels of mesentery fat than disturbed fish. Our results demonstrate that yellow perch growth can be significantly affected by disturbance level and lighting conditions. These factors should be taken into consideration when developing culture strategies to maximize the growth of yellow perch reared under intensive culture conditions.     

Effects of decreases in photoperiod on growth and bimodality in Atlantic salmon Salmo salar L.

Two experiments were performed to study the relative significance of the absolute daylength and the change in photoperiod on the growth and development of bimodality in juvenile Atlantic salmon Salmo salar L. In Experiment A juveniles were reared on 24 h daily light until they were seven months old (65–82 mm in length after size grading). They were then divided into six groups and subjected to six photoperiods (6, 9, 12, 15, 18 and 24 h of light). In Experiment B the decrease in photoperiod was made in two steps. First, the day length was reduced to 18 and 21 hours, three months after first feeding when the weight of the juveniles averaged 2.5 g and one group was kept under 24 hour daily light. Two months later, each of these treatment groups was subdivided to produce new groups of juveniles (65–82 mm in length) under 6, 9 and 12 h of daily light. Irrespective of whether the photoperiods were reduced in one or two steps, groups held under short-day photoperiods, 6–12 h, grew significantly slower (Exp. A) and showed higher proportions of lower modal group fish (Exp. B) than groups treated with long-day photoperiods, greater than 12 h. There were low proportions of lower modal group fish among juveniles larger than 75 mm at the dates of decreases in daylength irrespective of photoperiod (Exp. B, 0–16%), and high or variable proportions among fish smaller than 75 mm, depending on photoperiod (Exp B. 32–71%). It is concluded that the growth response of juvenile Atlantic salmon changes in the range of 12–15 hours of daily light. This mechanism is probably linked to the size of the parr and is one important reason for the development of bimodal length-frequency distributions.     

A closed water recirculation system for ecological studies in marine fish larvae: growth and survival of sea bass larvae fed with live prey

This paper describes the suitability of a closed recirculation system to study the development of fish larvae in a strictly controlled environment, where only feeding was varied (fed, starved, delayed and late fast treatments). The system served both as an incubator and hatchery. The time variation of physical and chemical parameters together with survival and growth of reared sea bass larvae (Dicentrarchus labrax) were studied over the first month of life. The recirculation design allowed for the maintenance of levels of ammonia, nitrite and nitrate below those cited as responsible for mortality or decreased feeding ability in other marine fish larvae. Almost no larval mortality occurred in the fed larvae from day 9 after hatching. The starved group of larvae showed a sharp decline in survival after 16 days of food deprivation. Larvae for which feeding was delayed until day 13 ceased dying 4 days after food was supplied. Fast feeding on days 24 and 25 had no effect on larval survival. Growth in length was similar during the first 2 weeks of larval life regardless of feeding treatment. Two days of late fast had no effect on larval growth. Growth patterns of fed larvae in this study were similar to those reported for larvae reared in flow through systems. We believe that survival and growth of the reared larvae was a direct function of diet, and that the type of rearing system did not adversely affect these parameters. The rearing design and the results obtained suggest that future nutritional studies of field-collected larvae will benefit from this kind of rearing experiment.     

Protein metabolism during sexual maturation in female Atlantic salmon (Salmo salar L)

Body composition and fractional rates of protein synthesis (percentage of the protein mass synthesized per day) were determined in female Atlantic salmon returning to the River Tay, Scotland in July and in October after a 95 day period without food, during which time the animals became sexually mature. During the 95 day period of starvation/sexual maturation the ventricle and red muscle remained as a constant proportion of fresh weight whereas the liver, gill and ovary increased and the stomach and white muscle decreased. Fractional rates of protein synthesis increased markedly in the liver, stomach and ovary during the period of starvation/sexual maturation. In the gill, ventricle and white muscle fractional protein synthesis rates increased slightly or remained constant. From the estimated rates of protein loss or gain in the various tissues it is concluded that there is considerable protein turnover and repartitioning of amino acids during the period of starvation and sexual maturation. The absolute rate of protein synthesis rates in the ovary indicates that this tissue made the largest contribution to the energy and amino acid demands of the fish, whilst most of the amino acids required for maturation of the ovary were derived from white muscle, principally as the result of increased muscle protein degradation.     

The effect of water temperature on growth parameters of intensively reared juvenile peled Coregonus peled

The effect of water temperature on growth and food intake of juvenile peled Coregonus peled was tested with specimens of initial age 75 days and 230 days posthatching (dph). The 75‐day group (initial body weight 0.6 ± 0.04 g) were reared for 63 days and 230‐day group (initial body weight 13.75 ± 2.93 g) for 42 days at temperatures of 13, 16, 19, 22 and 25°C under 12:12 L:D photoperiod. The optimal temperature range for the 75 dph fish was found to be 19–22°C. The fish reached final mean weight of 9.7 ± 2.5 g at 19°C and 9.0 ± 2.7 g at 22°C. Final mean weight of 230 dph fish did not differ significantly among temperature groups. Mortality increased at higher temperatures, with the critical temperature of 25°C for both age groups. Maximum food intake (19.0 ± 4.7, 18.8 ± 5.2, 18.6 ± 4.6 g kg^?1biomass) was observed in groups reared at temperatures of 19, 22 and 25°C with no significant differences among groups.     

Effects of rearing density on sexual maturation and growth in sea-cage reared Atlantic salmon, Salmo salar L.

Abstract. Paired subgroups of fish were derived in January from each of two parent sea-cages of Atlantic salmon, Salmo salar L. The proportion of fish which later became sexually mature in each parent group, after one winter (as grilse) and under commercial rearing density, was determined. Maturity rates in the subgroups, reared in sea-cages at lower density, were significantly greater than in the parent groups. Rearing at reduced density was associated with increased growth in some, hut not all, comparisons. Periodic anaesthesia, handling and sampling of blood for steroid hormone determinations did not consistently affect maturation rate or growth among fish in one of each pair of subgroups. Sexual development was assessed by determining levels of the steroid hormones 11-oxotestosterone or 17β-oestradiol in samples of blood serum taken monthly from individually marked fish in one of each pair of subgroups. Between February and April specific growth rates in maturing male grilse were significantly higher than in fish subsequently shown to have remained immature. Growth rates in maturing female grilse differed similarly between March and April. Between July and August, however, growth rates of non-maturing salmon exceeded those of grilse.