Induced maturation and spawning of domestic and wild striped bass, Morone saxatilis (Walbaum), broodstock with implanted GnRH analogue and injected hCG

Abstract. A domestic striped bass. Morone saxatilis (Walbaum), broodstock was established by rearing fish to sexual maturity in ponds. A method was developed to reproduce the domestic females, and also wild females too immature to be successfully induced to spawn with injected human chorionic gonadotropin (hCG). The fish were implanted with pellets containing 100–150μg of a synthetic analogue of mammalian gonadotropin reieasing-hormone, [D-Ala⁶- Pro⁹-NEt]-LHRH (mGnRHa), in a matrix of cholesterol (CH) and cellulose. They were implanted with one fast hormone-release (80% CH) pellet and one slow hormone-release (95% CH) pellet and allowed to mature for 1–3 days, until they entered the process of final oocyte maturation and were induced to ovulate or spawn with an hCG injection. The secondary hCG injection was found to be necessary to speed the maturation of the wild fish; they otherwise would succumb to the stresses of capture, handling and confinement before they could be spawned. The total mGnRHa dosages used ranged from 33 to 111μg mGnRHa/kg body weight, and the hCG doses were either 165 or 330 IU hCG/kg body weight. Using the combined mGnRHa implant-hCG injection technique, fry production rates were comparable to those obtained using fully mature wild females taken directly from their spawning grounds.     

Hormone Induced Spawning of Summer Flounder Paralichthys dentatus

During their first year in captivity, summer flounder Paralicthys denratus were induced to spawn with gonadotropin releasing hormone analogue (GnRHa) implants, injected carp pituitary extract (CPE) or human chorionic gonadotropin (hCG) injections. The percentage of fertile eggs was greatest (69%) in CPE-treated females. CPE, but not GnRHa or hCG, was capable of stimulating oocyte growth (increased follicle diameter during vitellogenesis) followed by ovulation. Fish with maximum ovarian follicle diameters between 180 and 435 μm at the initiation of CPE injections produced the greatest percentage of fertile eggs. For most females, fertilization rate was greatest for the first batch of eggs ovulated. The mean fertilization rate for the first spawn of CPE-treated fish was 42% compared with 14% for the second spawn from the same fish. Fish with maximum initial follicle diameters of 585 40 μm that were implanted with GnRHa ovulated the greatest number of eggs, but fertility was low and variable. Approximately 35% of females injected with hCG ovulated a limited number of eggs, but only one hCG-treated female produced fertile eggs. Only a limited number of spermiating males were available for spawning trials. Hormone treatments used on females were ineffective for inducing or maintaining spermiation in male summer flounder.     

Induced Ovulation of Southern Flounder Paralichthys lethostigma Using Gonadotropin Releasing Hormone Analogue Implants

Implanted pellets that provide a sustained release of [D-Ala⁶ Des-Gly¹⁰] LHRH-ethylamide (GnRHa) were used to induce maturation and ovulation of Southern flounder Paralichthys lethostigma . Of the 12 females whose ovaries contained follicles with a maximum diameter ≥500 μm, 11 ovulated for the first time within 90 h of hormone implantation. Only 1 fish with a maximum follicle diameter less than 500 μm ovulated within 2 wk after implantation. Ovulated eggs were manually stripped from the females and mixed with sperm from several males. Most females were spawned 1 to 3 times on consecutive days with variable fertility. One female was spawned 11 times producing 668,000 eggs. Fertility was evaluated by examining the incubated eggs for early stages of embryonic cleavage. The percentage of fertile eggs in subsamples of incubated eggs ranged from 7–95%. The results indicate that GnRHa implants can be used to induce repeated ovulation in this species. The variability in fertility is discussed in relation to egg quality.     

Reproductive development, GnRHa-induced spawning and egg quality of wild meagre (Argyrosomus regius) acclimatised to captivity

The objective of the study was to acclimatise wild-caught meagre (Argyrosomus regius) to captivity to produce viable eggs for aquaculture production. Twelve meagre (3 males and 9 females, mean weight?=?20?±?7?kg) were caught and transported to a land-based facility on 26 October 2006. During, March to June 2007, all three males were spermiating and five of the nine females were in vitellogenesis with mean maximum oocyte diameter ≥550?μm. No spontaneous spawning was observed. Two hormone treatments, either a single injection of gonadotropin-releasing hormone agonist (GnRHa, 20?μg?kg(-1) for females and 10?μg?kg(-1) for males) or a slow-release implant loaded with the same GnRHa (50?μg?kg(-1) for females and 25?μg?kg(-1) for males), were used to induce spawning on three different dates on 26 March 2007, 4 May 2007 and 18 April 2008. From each spawning event, the following parameters were determined: fecundity, number of floating eggs, egg size, fertilisation and hatching success, unfed larval survival, and proximal composition and fatty acid profile of the eggs. In 2007, two females that were injected on 26 March and 4 May spawned a total of 5 times producing 9,019,300 floating eggs and a relative fecundity of 198,200 eggs?kg(-1) and two different females that were implanted on the same dates spawned 14 times producing 12,430,000 floating eggs and a relative fecundity of 276,200 eggs?kg(-1). In 2008, a pair that was implanted spawned five times producing a total of 10,211,900 floating eggs and a relative fecundity of 527,380 eggs?kg(-1). The latency period was 48-72?h. Parameters were compared between hormone treatments, date of hormone induction and parents determined by microsatellites. Percentage hatch and egg size were 70?±?0.3% and 0.99?±?0.02?mm, respectively, for GnRHa-implanted fish and were significantly higher (P?相似文献   

Oogenesis and relevant changes in egg quality of abalone Haliotis discus hannai during a single spawning season

Oogenesis of abalone Haliotis discus hannai was examined histologically during a single spawning season using broodstock of various maturation conditions, which were controlled by effective accumulative temperature (EAT). The quality of eggs spawned was determined in relation to oogenesis. For histological examinations, three to five females were sacrificed at 300, 600, 850, 1050, and 1150 °C days EAT, without induction of artificial spawning. Other females were successfully induced to spawn at 700 °C days EAT and were reared following spawning. Three of these females were then sacrificed every 200 °C days EAT until 1300 °C days EAT. Gonad histology showed that two oocyte cohorts matured in H. discus hannai ovaries during a single spawning season. One mature oocyte cohort could be spawned in multiple times. The second oocyte cohort started developing after the first oocyte cohort had been spawned or reabsorbed, and became fully mature 400 °C days EAT after the first cohort was depleted. For egg quality measurements, three to five females were successfully induced to spawn at 850, 1050, 1150, 1900, and 2350 °C days EAT (Experiment 1). Three females were induced to spawn twice, at 700 and 1500 °C days EAT, resulting in two batches of eggs from the same individuals (Experiment 2). Total lipid and protein content of eggs were measured and were greater in eggs from the second cohort than in eggs from the first cohort. No carbohydrates were detected in eggs and there was no difference in cytoplasm volume between the two cohorts. In hatcheries producing H. discus hannai, it is important to increase post-larval starvation tolerance by increasing the quality of eggs, to yield higher and more consistent survival. The results of this study suggest that H. discus hannai hatcheries should use eggs from the second oocyte cohort, which are of higher quality, rather than eggs from the first oocyte cohort.     

High‐quality spontaneous spawning in greater amberjack (Seriola dumerili,Risso 1810) and its comparison with GnRHa implants or injections

Production of sufficient high‐quality eggs of greater amberjack (Seriola dumerili) still constitutes the main bottleneck for commercial production of this species. The main objective of this study was to compare the quality of spontaneous spawn of greater amberjack with those obtained by either GnRHa injection or GnRHa implant protocols. Captive amberjack broodstock were distributed in three circular tanks of 40 m³. Broodstock from Tank 1 were not hormonally induced and spawned spontaneously, whereas those of Tank 2 were intramuscularly injected with GnRHa (20 µg/kg body weight) and those of Tank 3 were given EV‐500 µg GnRHa implants. The number of eggs per spawn obtained in the broodstock without hormonal treatment was larger than in those obtained with injections or implants. Egg quality was best in broodstock with spontaneous spawn, followed by GnRHa‐injected fish and then GnRHa implants. Besides, size of larvae from control and injected broodstock was similar between them and significantly higher (p < 0.01) than those from GnRHa implant spawn. Overall, this study showed that it is possible to obtain very high‐quality spontaneous spawn in greater amberjack, providing the adequate conditions. Furthermore, GnRHa weekly injections lead to similar egg viability and hatching rates than spontaneous spawn and higher fertilization rates than GnRHa hormonal implants, which is better than in previous studies.     

Induction of Spawning in the Sea Cucumber Holothuria scabra (Echinodermata: Holothuroidea)

With the advent of sea cucumber aquaculture in the South Pacific region, a reliable method is needed to induce large numbers of animals to spawn in captivity. Broodstock of the sea cucumber Holothuria scabra , collected from Stradbroke Island, Moreton Bay (27°90'N, 153°24'E) Australia, during the reproductive season from October to January, were used in spawning trials. During the 1997–1998 summer between one to five weeks of captivity, 100% of animals were induced to spawn in four trials at dusk on or close to a new or full moon, using nine males and nine females contained in a Reln tank and 30 cm of filtered sea water, using a 3–5 C temperature shock. H. scabra was induced to spawn in small numbers during the 1996–1997 summer despite a marked degree of weight loss, and all animals spawned during 1997–1998 with minimal loss of weight. The difference in the number of spawned eggs between animals of similar size and mean numbers of spawned eggs in consecutive trials decreased the longer animals were held in captivity before spawning. The hatch rate of eggs was reduced significantly for broodstock held for more than one month. Hatch rate and numbers of spawned eggs are important indicators of egg viability of broodstock maintained in captivity for an extended period.     

Effects of Broodstock Size and Source on Ovarian Maturation and Spawning of Penaeus monodon Fabricius from the Gulf of Thailand

The effects of broodstock source (pond-reared and wildcaught from shallow waters) and prawn size (large—weight >120 g, and small-weight < 110 g) on ovarian maturation and reproductive success of Penueus monodon were evaluated. Large females underwent stage IV ovarian maturation and spawned with greater success than did small prawns. Both pond-reared and wildcaught females of the same size exhibited comparable maturation and spawning success. Large females rematured and spawned more frequently than small ones. Total eggs produced by large prawns was significantly greater than for small prawns; nevertheless, prawn source and size had no significant influence on amount of eggs spawned per spawning event. Egg quality varied greatly in terms of percent fertilization, hatch rate, and metamorphosis to first protozwa stage.     

Voluntary Spawning of Captive Nassau Groupers Epinephelus striatus in a Concrete Raceway

Nassau groupers Epinephelus striatus held in a 37-m³ concrete raceway were conditioned to spawn 3 mo later than in their home waters. After being held in the raceway for 15 mo, four female and two male groupers spawned voluntarily over a 4-d period in March 1994, producing 10.3 million eggs. By December 1994, two females had been removed. During March 1995, one of the remaining two females spawned on three consecutive days (60 cm TL, 1,172,000 eggs) and the other only on the third day (47 cm TL, 488,000 eggs). In April 1995, three females (including one held in isolation for 6 mo, then replaced 6 d before the first spawn) produced more than 9.8 million eggs in 4 d. The isolated female spawned 8 d after being placed in a cage in the raceway and 4 d after release in the raceway.
Individual females spawned as many as nine times a day for 1–4 d. Spawning occurred from 3.5 d before until 8.5 d after the full moon. A 30-d interval elapsed between March and April 1995 spawning periods. Fertilization was in the range 83–100% and hatching 90–100%. Spawns occurred in a temperature range of 23.1–27.9 C; however, based on spawning frequency and volume and on egg development, 24–27 C seems most suitable. These results and other evidence support the view that Nassau groupers can be conditioned to spawn any month of the year, mainly by manipulating temperature.     

Induced Spawning of Wild American Shad Alosa sapidissima Using Sustained Administration of Gonadotropin-Releasing Hormone Analog (GnRHa)

American shad Alosa supidissima broodstock were collected from the Susquehanna River during their spawning migration. Mean volume of expressible milt (± standard deviation) was 2.5 (±1.7) mL/kg body weight; mean spermatozoid count was 66.2 ± 10⁹ (±163 ± 10⁹) spermntozoa/mL; and duration of 50% motility was 36.5 (±10.3) see. Ovarian biopsies indicated the presence of oocytes of various sizes (200–2,000 μm in diameter) and stages of development. Fish were implanted with a delivery system loaded with gonadotropin-releasing hormone analog (GnRHa) and started spawning 2 d after treatment. Fertile eggs were collected daily for the next 9 d, for a total of 50,100 eggs/kg body weight with a mean fertilization success of 62%. Upon cessation of spawning, the ovaries of all females still contained large numbers of oocytes at various stages of development, as at the beginning of the experiment, but with a greater number of atretic oacytes. Our observations show that American shad have an asynchronous ovarian development, and treatment with a GnRHa delivery system is effective in inducing several successive spawns of fertile eggs.     

Preliminary Studies of Artificial Spawning of Channel Catfish as Male-Female Pairs or All-Female Groups in Recirculating Systems

Abstract— Channel catfish Icralurus punctatus are commonly spawned for research purposes by pairing of a hormonally treated female with a male in flow-through aquaria. A technique that allows hormonal induction of ovulation in females without pairing would accelerate genetic improvement and production of hybrid catfish. Over a 3-yr period (1994, 1995, and 1996) we conducted a series of trials to demonstrate the potential for artificial spawning in recirculating systems, and in 1996 we included trials with grouped females in addition to male-female pairs. Females were induced to spawn with injection of synthetic leuteinizing hormone-releasing hormone, and those that ovulated were stripped and the eggs were artificially fertilized. During 1994 and 1995, all fish were spawned by pairing, and in 1996, half of the females were spawned by pairing and half were grouped in tanks without males. Spawning success (percent of females that produced eggs), latency (time between injection and ovulation), and percent fertilization were observed for the paired and grouped trials. Spawning success was 36% in 1994 (N= 36). 22% in 1995 (N= 54). 41% in 1996 (N= 27). and 58% for grouped females (N= 26). The latency period was 113 ± 69 h in 1994, 109 ± 57 h in 1995, 44 ± 8 h in 1996, and 50 ± 9 h for grouped females. Percent fertilization was 16 ± 26% for eggs stripped in 1994, 72 ± 25% in 1995, 43 ± 20% in 1996, and 16 ± 37% for grouped females. In 1995, water quality problems were associated with high mortality of females (24 of 44 females; 4 of 44 males). The metabolic demands of final oocyte maturation in combination with methemoglobinemia caused by high nitrite levels could account for the increased vulnerability of females. These trials indicate that with adequate biofiltration, artificial spawning is possible in recirculating systems and with females grouped rather than paired. Further research on hormone dosage and timing of egg stripping will increase the utility of grouped spawning of channel catfish.     

异齿裂腹鱼人工规模化繁殖技术研究

2010年4～6月,对野生异齿裂腹鱼(Schizothorax o' connori)人工规模化繁殖技术进行研究,并初步进行产后亲鱼恢复培养技术研究.对108尾雌鱼进行干法人工授精,共采卵104万多粒,孵出仔鱼62万多尾.其中45尾雌亲鱼自然成熟,共采卵46.8万多粒,平均受精率和孵化率低于人工催产雌鱼卵.人工催产83...     

Volitional Spawning of Black Sea Bass Centropristis striata Induced with Pelleted Luteinizing Hormone Releasing Hormone-Analogue

The black sea bass is a high‐value marine serranid and is a prime candidate for intensive cultivation. Reliable methods for controlled spawning are needed to accelerate the development of hatchery technologies that result in mass production of healthy juveniles. During 1998–2001, spawning studies were conducted at The University of North Carolina at Wilmington (UNCW) and at the South Carolina Department of Natural Resources (SCDNR), Charleston, using pelleted luteinizing hormone releasing hormone analogue (LHRH‐a). From April through July 2001, 28 vitellogenic‐stage females, with mean oocyte diameters (MOD) ranging from 277–448 μm, were implanted with a 95% cholesterol‐5% cellulose pellet containing LHRH‐a (‐50 μg/kg body wt) at UNCW. In 10 individual spawning trials, females with MOD of 305–448 μm and maximum oocyte diameter × 475 μm spawned volitionally beginning 2–3 d post‐implantation (PI) and continued spawning over an average of 1.9 d (range = 1–4 d). Individual females released a mean total of 149,000 eggs (117,000 eggs/kg) with a mean buoyancy rate of 40.5% (floaters). Fertilization and hatching rates were 98% and 27.2% of floaters, respectively, yielding 14,600 yolksac larvae/female (12,600 yolksac larvae/kg body wt), and overall egg viability averaged 8.9%. In eight group spawning trials (2–3 females/group), average performance of females, including fecundity (103,800 eggs/female; 105,500 eggs/kg body wt), buoyancy rate (42.5%), fertilization and hatching rates (97.7% and 24.3% of floaters), numbers of yolksac larvae produced (10,900 yolksac larvae/female; 10,100 yolksac larvae/kg body wt), and overall egg viability (10.6%) was comparable to what was seen in individual spawning trials. From 1998–2000, a total of 58 vitellogenic stage (70% of oocytes 500 pm) females were implanted with pelleted LHRH‐a (‐50 μg/kg body wt) in nine group spawning trials (2–19 females/group) at SCDNR. Volitional spawning typically began 18–42 h PI and recurred every 1–3 d for an average duration of 9 d. Female groups released a mean of 560,000 eggs (84,000/female; 132,000/kg body wt) over the spawning period, with mean buoyancy rate of 25.7% floaters. Fertilization and hatching rates were 17.7% and 11.6 % of floaters, respectively, yielding 4,300 yolksac larvae/female (4,600 yolksac larvae/kg body wt). Overall egg viability was 2.9%. Captive wild‐caught black sea bass were induced to undergo repetitive volitional spawning by implantation of pelleted‐LHRH‐a, consistent with a multiple clutch group synchronous pattern of ovarian development. Group spawning appears to be a practical way to compensate for variable fecundity and egg viability of individual females. Research is needed to identify optimum hormone treatments and eligibility requirements.     

Spawning induction of blue mackerel <Emphasis Type="Italic">Scomber australasicus</Emphasis> and eastern little tuna <Emphasis Type="Italic">Euthynnus affinis</Emphasis> by oral administration of a crude gonadotropin-releasing hormone analogue

Scombridae species, such as tunas and mackerels, often do not spawn in land-based fish tanks without hormone treatment. To induce spawning in various fishes, a gonadotropin-releasing hormone analogue (GnRHa) is often administered by pellet implantation. Noninvasive administration is desired to induce spawning in scombrids that are sensitive to handling stress. Spawning induction by oral administration has been reported in several fishes, yet this method has not been put into practice in the aquaculture industry since a considerable amount of GnRHa is needed. Utilization of peptide synthesizers is widespread, and antigen-grade GnRHa (AgGnRHa) produced by a custom-peptide supplier is approximately 100-fold cheaper than conventional reagent-grade GnRHa (RgGnRHa), although the purity of AgGnRHa is lower. Here, we confirmed that the spawning induction potency of AgGnRHa was similar to that of RgGnRHa by pellet implantation in blue mackerel Scomber australasicus. Oral administration of AgGnRHa [6.0 mg/kg body weight (BW) per day] showed an equivalent ability to induce spawning of the mackerel as pellet implantation (0.1 mg/kg BW). We could also induce spawning of eastern little tuna Euthynnus affinis by oral administration of the AgGnRHa. Further, the obtained eggs showed higher survival. Thus, the oral delivery of AgGnRHa could be a powerful tool to induce spawning in Scombridae.     

Spawning induction of pejerrey Odontesthes bonariensis in captivity using sustained‐release gonadotropin releasing hormone agonist implants

The aim of this study was to induce and synchronize spawning of pejerrey Odontesthes bonariensis (Valenciennes, 1835), using gonadotropin releasing hormone agonist (GnRHa) implants. In the first experiment, the ovarian condition was assessed by ovarian biopsies and the measurement of the genital pore width (GPW). Females having the leading clutch of oocytes with a diameter of around 800–900 μm and a GPW between 4.5 and 5.5 mm were treated with GnRHa implants. Eighty per cent of females spawned between 2 and 9 days after treatment, 12 days earlier than 20% of the fish in the control group that presented signs of spawning activity. In order to avoid any possible ovarian injury and/or stress by the catheterization procedure, in a second experiment, females were selected only by visual inspection of the abdomen and GPW measurement. As in experiment 1, 80% of females spawned between 2 and 8 days after treatment, 8 days earlier than 30% of the fish that spawned in the control group. In both experiments, fertilization and hatching success were similar between control and GnRHa‐treated groups. These results clearly demonstrated that GnRHa implantation can advance and synchronize ovulation and spawning in pejerrey without affecting egg quality.     

Reproductive Performance of Pigmented and Albino Female Channel Catfish Induced to Spawn with HCG or Ovaprim

Reproductive performance of albino and pigmented channel catfish ( Ictalurus punctarus ) females was compared when spawning was induced with HCG (human chorionic gonadotropin) or Ovaprim ³ (domperidone and [d-Ala⁶, Pro⁹ NEt]-luteinizing hormone-releasing hormone). In 1985, only HCG was used to induce spawning. Albino females required more injections, had a longer latency period from time of first injection to spawning, and had lower spawning success (30%) than pigmented females (77%). No differences were observed between albino and pigmented females for time-of-day of spawning, number of eggs obtained by manual stripping, and number of eggs/kg body weight. In 1988, HCG, Ovaprim, and saline (control) were used to induce spawning. HCG induced spawning in 80% of albino and 71% of pigmented females. Ovaprim induced 67% of pigmented females to spawn, but only 2 of 5 albino females spawned. One of four pigmented females injected with saline spawned. Albino females yielded 40–50% fewer eggs/kg body weight than pigmented females. Other performance characteristics for albino and pigmented females were similar whether injected with HCG or Ovaprim. High temperatures encountered during the 1985 spawning season my have had a differential effect on albino and pigmented fish and may account for some differences in spawning success.     

Application of controlled-release,GnRHa-delivery systems in commercial production of white bass X striped bass hybrids (sunshine bass), using captive broodstocks

Hatchery-produced white bass (Morone chrysops) and striped bass (M. saxatilis) reared to maturity in a commercial aquaculture facility, were successfully spawned using controlled-release delivery systems containing the gonadotropin-releasing hormone analog DAla⁶, Pro⁹[NEt]-GnRH (GnRHa). Two-year-old white bass females (mean weight, 0.81 kg) were implanted with different polymer-based, GnRHa delivery systems at doses ranging from 40 to 89 μg GnRHa kg⁻¹ body weight. GnRHa treatment on 20 February 1994, when females contained oocytes up to 720 μm in diameter, induced ovulation of all fish between 35 to 82 h after treatment. The white bass eggs produced were fertilized with sperm from striped bass for the production of sunshine bass. An average of 294500 eggs kg⁻¹ were produced, with a mean fertility of 81.2%, 24 h survival of 46.5%, and overall hatching success of 45%. Survival from hatch to 30 days post-hatch was 78% and the fry weighed between 0.07 and 0.1 g. Overripening of eggs began within 1 h from ovulation and maximum fertilization (60%) was observed when eggs were stripped 0.5 h after ovulation. Fertilization success decreased thereafter to 31% and 10% by 1 h and 3 h after ovulation, respectively. Control fish not treated with GnRHa did not show any signs of final oocyte maturation during the period of the study. GnRHa administration via controlled-release delivery systems appears to be a very effective method for inducing high fecundity ovulation of captive white bass broodstocks, and producing eggs of high fertility and hatching success.     

Reproductive biology of captive bullseye puffer (Sphoeroides annulatus), LHRHa induced spawning and egg quality

Few mature female bullseye puffer have been observed to spawn in captivity. The ovary appears to develop to late vitellogenesis, but not to complete final oocyte maturation (FOM). Luteinizing hormone releasing hormone analogue (LHRHa) treatment induced the spawning of good quality eggs in both wild and captive brood fish.     

Oocyte maturation and ovulation in the Atlantic halibut, Hippoglossus hippoglossus (L.), examined using ultrasonography

High resolution ultrasound scanning was tested as a non-invasive technique for monitoring oocyte maturation and ovulalion in the Atlantic halibut Hippoglossus hippoglossus (L.). Female broodstock halibut were examined using a 7.5-Mhz linear ultrasound transducer, prior to and during spawning. Representative images of halibut ovaries are presented and discussed. Individual oocytes of spawning females were discernible during oocyte final maturation, due to the large increase in volume caused by water uptake. The yolky (vitellogenic) cocytes of pre-spawning fish were more reflective to ultrasound than hydrating oocytes. The resulting differences in depth of ultrasound penetration permitted easy distinction of pre-spawning from spawning females. In addition, short-term changes in the depth of ultrasound penetration were observed during repeated scanning of a spawning female, owing to progressive hydration of the oocyte batch destined for ovulation. Although of similar diameter, hydrating oocytes in the ovarian tissue could be discerned from eggs in the ovarian lumen because of the different acoustic properties of the surrounding media. The findings of the present study are considered promising for the future routine use of ultrasonography in halibut broodstock management.     

Biofloc technology in intensive broodstock farming of the pink shrimp Farfantepenaeus duorarum: spawning performance,biochemical composition and fatty acid profile of eggs

A 45‐day trial was performed to evaluate the effect of biofloc technology (BFT) with or without fresh food (FF) supplementation during pre‐maturation period on Farfantepenaeus duorarum spawning performance, biochemical composition and fatty acid profile of eggs as compared with conventional clear‐water system (CW+FF). Females raised in biofloc and that received FF supplementation (FLOC+FF) achieved better spawning performance in terms of number of eggs per spawn (49 × 10³), number of eggs per spawn per g of spawner's body weight (2.1 × 10³) and egg size (~275 μm) as compared with CW+FF (23 × 10³, 1.1 × 10³ and 263 μm respectively), but both treatments did not vary from FLOC (P > 0.05). High spawning activity was also observed in biofloc system as compared with clear‐water system as shown in number of spawns per ablated female (2.2–3.0 versus 0.6) and percentage of females that spawn at least once (80–82 versus 25%). Biochemical composition of eggs presented no significant differences among treatments. FA profile of eggs indicated that high spawning activity performed by females in FLOC+FF treatment was reflected in lower mean levels of EPA, DHA and sum of polyunsaturated fatty acids (n‐3) and (n‐6). The better reproductive performance demonstrated by females raised in biofloc justified the application of this technology in F. duorarum broodstock.