松江鲈胚胎及胚后发育研究

采用人工繁育的松江鲈子一代为亲本，人工授精，在水温6℃、盐度32的条件下人工脱黏孵化，观察了胚胎发育。结果显示：松江鲈受精卵经过7 h进入卵裂期，经过2 d发育至囊胚期，5 d进入原肠期，经过9 d发育至眼囊期，17 d出现围心腔，22 d时肌节形成，29 d时体色素开始沉积，30～35 d孵出。在水温11.37℃～16.88℃、盐度32的条件下进行仔稚鱼培育。初孵仔鱼平均全长6.98 mm，出膜后4 d卵黄囊完全吸收，出膜后28 d背鳍、腹鳍、胸鳍和尾鳍发育完全，体表黑色素沉积增加，进入稚鱼期，出膜后55 d身体不透明，进入幼鱼期。结果显示，由于水温等环境因素的原因，胚胎发育与胚后发育各个阶段所需的时间与前人的研究结果存在一定差异。     

哲罗鱼（♀）与细鳞鱼（♂）杂交种胚胎及仔稚鱼发育

通过性激素药物诱导和人工繁育技术对哲罗鱼(♀)(Hucho taimen)与细鳞鱼(♂)(Brachymystax lenok)进行属间远缘杂交,并对杂交种胚胎及仔稚鱼的发育进行初步研究。结果表明:在水温6.2～8.9℃条件下,哲罗鱼(♀)×细鳞鱼(♂)的杂交受精卵完成胚胎期发育所需的有效积温为5806.70℃·h,整个胚胎发育过程可分为6个阶段,24个发育分期。刚破膜的仔鱼不具有游泳能力,全身透明,体循环清晰可见;7d后卵黄囊期仔鱼口裂明显,头顶部和腹部开始变得浅黄,尾鳍分化不断完成;17d后,仔鱼开始上浮,卵黄囊基本吸收完全,仔鱼具有游泳能力,鳍条和腹部鳞片开始不断分化。上浮40d后仔鱼发育成稚鱼,脂鳍分化和身体两侧鳞片覆盖基本完毕,幼鲑斑开始出现。根据研究结果可以初步断定,该杂交种的胚胎发育速度介于双亲之间,稚鱼期基本具备成鱼形态特征,早期杂交种外部形态略偏向于哲罗鱼,但仔稚鱼期生长较双亲快,推断这种杂交优势的贡献力可能来源于母本。     

云纹石斑鱼胚胎发育及仔、稚、幼鱼形态观察

对云纹石斑鱼Epinephelus moara胚胎发育及仔、稚、幼鱼形态进行了观察与研究,详细描述了各发育期的形态特征和发育时间。结果表明:1)在水温22±0.2℃、盐度30、溶氧7.8mg/L、pH8.25的条件下,云纹石斑鱼的受精卵历时38h 17min开始孵化出膜。胚胎发育可分为受精卵、卵裂、原肠、神经胚和器官形成及出膜6个阶段,受精、胚盘形成、2细胞等28个时期。2)在水温23±1℃,盐度30±3,DO≥5mg/L,pH8.0±0.5的海水中,培育至5d,卵黄囊完全消失,成为后期仔鱼;培育至27d,发育最快的云纹石斑鱼结束仔鱼期,进入稚鱼期;培育至65d,发育最快的稚鱼完成变态,成为幼鱼。胚后发育过程主要是根据卵黄囊、鳍膜、鳞片、体色及第1腹鳍棘与第2背鳍棘相对长度的变化分为仔鱼、稚鱼和幼鱼3个时期。其中仔鱼期又根据其卵黄囊的有无划分为前期仔鱼和后期仔鱼。     

半刺厚唇鱼胚胎与胚后发育观察

通过对半刺厚唇鱼[Acrossocheilus(Lissochilichthys)hemispinus]胚胎及胚后发育进行观察,详细描述了从受精卵到稚鱼期发育时期的时序和形态特征.结果表明:半刺厚唇鱼成熟卵圆形,卵径1.74～1.97 mm,黄色或桔黄色.在25 ～28℃水温条件下,孵化时间为62 h,刚出膜仔鱼全长5.6～7.2 mm.在26～28℃水温条件下,出膜后仔鱼7日龄初次摄食;9日龄时卵黄囊完全消失;15日龄时,进入稚鱼期:25日龄时,鳞片形成,进入幼鱼期.仔、稚鱼体侧都具有7条明显的黑褐色横向条纹,成鱼条纹消失.     

驼背鲈(Chromileptes altivelis)的胚胎发育及仔、稚、幼鱼形态观察

对驼背鲈(Chromileptes altivelis)的胚胎发育及仔、稚、幼鱼的形态特征进行了详细的观察与研究,描述了从受精卵到仔、稚、幼鱼各发育期的时间和形态特征变化。结果表明,在水温25-26℃、盐度30的海水中,受精卵历时27 h 25 min完成整个胚胎发育过程,经历从卵裂、囊胚、原肠、神经胚到肌节形成、各器官的逐渐形成、变化、完善等一系列的胚胎发育和变化过程;根据其卵黄囊消长情况、鳞片的覆盖状态、体色发生的不同变化以及第二背鳍和腹鳍的消长,将胚后发育分为仔、稚、幼鱼3个阶段。在水温22-26℃、盐度29-31、DO≥5 mg/L的条件下,2-3 d仔鱼卵黄囊消失,开口摄食;生长发育至31 d,仔鱼已变态进入稚鱼期;培育至57 d,稚鱼完成变态,成为幼鱼。第二背鳍棘和腹鳍棘的生长与收缩等石斑鱼类早期发育的共性生长特征及其体表特性体色变化特征为驼背鲈胚后发育过程中最明显的特征。     

大西洋牙鲆(Paralichthys dentatus)仔、稚、幼鱼形态观察

文中对大西洋牙鲆仔、稚、幼鱼各期发育时间及特征进行观察记录,并对各发育阶段进行显微摄像。大西洋牙鲆室内人工育苗水温18℃～22℃,盐度30,pH8.2,光控500Lx左右。饵料为强化的轮虫、卤虫无节幼体和配合饲料。初孵仔鱼肠道细而直,孵化后3d～4d肛门开通并开口摄食,6d～7d卵黄囊吸收完毕,仔鱼前期阶段结束。仔鱼后期阶段,消化道弯曲,冠状幼鳍完全形成,右眼开始上升。稚鱼期右眼完全迁移至左侧,变态完成,营底栖生活。幼鱼期基本具有成鱼的外部形态和习性。     

驼背鲈(Chromileptes altivelis)的胚胎发育及仔、稚、幼鱼形态观察

对驼背鲈(Chromileptes altivelis)的胚胎发育及仔、稚、幼鱼的形态特征进行了详细的观察与研究,描述了从受精卵到仔、稚、幼鱼各发育期的时间和形态特征变化。结果表明,在水温25-26℃、盐度30的海水中,受精卵历时27 h 25 min完成整个胚胎发育过程,经历从卵裂、囊胚、原肠、神经胚到肌节形成、各器官的逐渐形成、变化、完善等一系列的胚胎发育和变化过程;根据其卵黄囊消长情况、鳞片的覆盖状态、体色发生的不同变化以及第二背鳍和腹鳍的消长,将胚后发育分为仔、稚、幼鱼3个阶段。在水温22-26℃、盐度29-31、DO≥5 mg/L的条件下,2-3 d仔鱼卵黄囊消失,开口摄食;生长发育至31 d,仔鱼已变态进入稚鱼期;培育至57 d,稚鱼完成变态,成为幼鱼。第二背鳍棘和腹鳍棘的生长与收缩等石斑鱼类早期发育的共性生长特征及其体表特性体色变化特征为驼背鲈胚后发育过程中最明显的特征。     

云纹石斑鱼(♀)×七带石斑鱼(♂)杂交子一代胚胎发育及仔稚幼鱼形态学观察

以云纹石斑鱼(Epinephelus moara)♀为母本,七带石斑鱼(E.septemfasciatus)♂为父本进行种间远缘杂交,系统观察了杂交子一代胚胎及仔稚幼鱼的生长发育及形态特征。对杂交子一代的胚胎发育按卵裂期、囊胚期、原肠胚期、神经胚期和器官形成期各阶段进行观察,在水温21～22.5℃、盐度29、pH 8～8.1的海水中,整个胚胎发育过程经35 h 20min完成。根据在卵黄囊期、第二背鳍棘和腹鳍棘生长消退过程、鳞片生长、体表色素变化的不同,观察比较了胚后发育的仔鱼期、稚鱼期、幼鱼期形态特征。鱼苗培育至58 d后完成了稚鱼至幼鱼的变态:初孵仔鱼4 d以前为内源性营养(卵黄囊仔鱼);4 d后开口摄食,为外源性营养;(42±2)d基本完成变态进入稚鱼阶段,(58±4)d全身被鳞,进入幼鱼期。同时,用同一母本(云纹石斑鱼)同批卵与同种雄鱼采集的精子授精后获得的受精卵作为对照组,进行孵化和仔稚幼鱼培育,与杂交子一代进行比较,结果发现杂交子一代在仔稚幼鱼阶段生长速度快于云纹石斑鱼,与七带石斑鱼相近。     

棕点石斑鱼(♀)×鞍带石斑鱼(♂)杂交子代胚胎及仔稚幼鱼发育的跟踪观察

本研究阐述了棕点石斑鱼(♀)×鞍带石斑鱼(♂)杂交子代(简称珍珠龙胆石斑鱼)的胚胎发育和仔稚幼鱼形态发育的特征及其养殖过程中的一些难点、要点,以期为今后苗种的规模化培育生产提供参考依据。通过对珍珠龙胆石斑鱼各个发育期连续取样,系统观察并记录各发育期的形态变化及生长特征。结果表明,1)在水温27-28℃条件下,历时25 h 25 min孵化出膜,整个发育过程划分为卵裂期、囊胚期、原肠胚期、神经胚期和器官形成期。2)在水温(27.0±0.5)℃、盐度30、p H 8的培育条件下,根据卵黄囊、第二背鳍棘和腹鳍棘的生长与伸缩及鳞片、体色的变化将胚后发育分为仔鱼、稚鱼、幼鱼3个时期。仔鱼期根据卵黄囊的有无分为前期仔鱼和后期仔鱼。初孵至孵化后4 d为前期仔鱼;孵化后5 d,仔鱼卵黄囊完全消失,成为后期仔鱼;孵化后32 d,50%的仔鱼进入稚鱼期;孵化后46 d,50%的稚鱼完成变态,成为幼鱼。初孵仔鱼的全长平均为(1.65±0.11)mm,发育至70 d时,幼鱼平均全长已达(75.47±0.19)mm。跟踪观察的结果发现,珍珠龙胆石斑鱼作为杂交子代,从受精到发育的各阶段均能健康正常地生长发育,且生长快速、抗病力强,具有"虎斑头、龙胆尾"的外型,具有明显的杂交优势。     

眼斑双锯鱼的人工繁育技术研究

在人工饲养条件下,模拟自然环境对野生眼斑双锯鱼Amphiprion ocellaris进行驯养使其达到性成熟、配对、产卵。显微镜下观察其胚胎发育的形态学变化。结果表明,眼斑双锯鱼的胚胎发育同大多数硬骨鱼类基本相似,属端黄卵盘状卵裂;在水温27.0±0.5℃条件下,经192～216h完成孵化;仔鱼在孵出的第2天开食轮虫,4～5d变态为稚鱼,开始投喂卤虫无节幼体,18～20d进入幼鱼期,45～50d开始投喂人工配合饵料及碎虾肉。     

Association between the interannual variation in the oceanic environment and catch rates of bigeye tuna (Thunnus obesus) in the Atlantic Ocean

The environmental processes associated with variability in the catch rates of bigeye tuna in the Atlantic Ocean are largely unexplored. This study used generalized additive models (GAMs) fitted to Taiwanese longline fishery data from 1990 to 2009 and investigated the association between environmental variables and catch rates to identify the processes influencing bigeye tuna distribution in the Atlantic Ocean. The present findings reveal that the year (temporal factor), latitude and longitude (spatial factors), and major regular longline target species of albacore catches are significant for the standardization of bigeye tuna catch rates in the Atlantic Ocean. The standardized catch rates and distribution of bigeye tuna were found to be related to environmental and climatic variation. The model selection processes showed that the selected GAMs explained 70% of the cumulative deviance in the entire Atlantic Ocean. Regarding environmental factors, the depth of the 20 degree isotherm (D20) substantially contributed to the explained deviance; other important factors were sea surface temperature (SST) and sea surface height deviation (SSHD). The potential fishing grounds were observed with SSTs of 22–28°C, a D20 shallower than 150 m and negative SSHDs in the Atlantic Ocean. The higher predicted catch rates were increased in the positive northern tropical Atlantic and negative North Atlantic Oscillation events with a higher SST and shallow D20, suggesting that climatic oscillations affect the population abundance and distribution of bigeye tuna.     

Growth performance,digestive enzyme activity and immune response of Japanese sea bass,Lateolabrax japonicus fed with fructooligosaccharide

In this experiment, a feeding trial was performed to determine the effects of fructooligosaccharide (FOS) on growth performance, digestive enzyme activity and immune response of Japanese sea bass, Lateolabrax japonicus juveniles (initial weight 38.3 ± 0.5 g), and the fish were examined following feeding with six levels of FOS (0, 0.5, 1, 2, 4 and 6 g/kg) for 28 days. Significant enhancement of weight gain (WG) and specific growth rate (SGR) was found in fish fed 1 g/kg FOS incorporated diets (p < .05), while the feed conversion ratio (FCR) in the 1, 2 g/kg FOS groups reduced significantly compared with the control (p < .05). Besides, the crude lipid in the 4, 6 g/kg FOS groups increased significantly compared with the control (p < .05). On the other hand, the erepsin and lipase activities significantly elevated in intestine of fish fed 2 g/kg FOS (p < .05) and the lysozyme activity in serum of fish fed 2 g/kg FOS were significantly higher than that in the control (p < .05). Moreover, the alkaline phosphatase activities in serum of fish fed 0.5, 1, 2 g/kg FOS were significantly higher than in control (p < .05). Regression analysis showed that the relationships between dietary FOS levels and either SGR, FCR, erepsin or lysozyme activities were best expressed by regression equations, and the optimal inclusion levels are 1.37, 1.80, 3.06, 3.11, 1.93 and 1.80 g/kg for SGR, FCR, erepsin, lipase, lysozyme and total superoxide dismutase activities, respectively. Overall, this study revealed that FOS incorporated diets could beneficial for L. japonicus culture in terms of increasing the growth, digestion and immune activities. Under the present experimental condition, the optimal supplementary level of FOS in the diet of L. japonicus is 1–3 g/kg.     

Protein and amino acid composition from the mantle of juvenile O ctopus vulgaris exposed to prolonged starvation

Protein and amino acid composition of the mantle of juvenile O ctopus vulgaris (Cuvier, 1797) during fasting for 27 days were determined. Average protein content of octopus mantle was of 711.19 ± 46.80 g kg^?1 DW, and it decreased with increasing fasting days. The non‐essential amino acids content was higher (486.18 ± 11.08 g kg^?1 protein) than essential amino acids (425.82 ± 9.15 g kg^?1 protein) at the start of the experiment (unstarved animals). The results suggest that the amino acid profile of the mantle where the most abundant amino acids are Arg, His, Lys, Gly, Leu and Pro could indicate a prolonged fasting condition (>20 days) or poor nutrition of O . vulgaris. This study supports the idea of using mantle for metabolic needs of starved O . vulgaris suggesting that the degradation pathway of amino acids to pyruvate and tricarboxylic acid cycle intermediates was favoured contrary to the degradation pathway of ketogenic amino acids. Special considerations should be taken concerning Thr, Ile, Ser, Ala, Asx (Asp, Asn), Glx (Glu, Gln) (because of their fast intake) and Lys and His (due to their stable contents) during a prolonged period of fasting.     

Involvement of gonadal steroids in final oocyte maturation of white perch (Morone americana) and white bass (M. chrysops): in vivo and in vitro studies

Plasma estradiol-17 (E₂), testosterone (T), 17,20-dihydroxy-4-pregnen-3-one (DHP) and 17,20,21-tri-hydroxy-4-pregnen-3-one (20-S) levels were measured by radioimmunoassay (RIA) in white perch (Morone americana) and white bass (M. chrysops) that were induced to undergo final oocyte maturation (FOM) with human chorionic gonadotropin (hCG). Plasma DHP levels increased in females of both species in association with oocyte germinal vesicle migration (GVM) and germinal vesicle breakdown (GVBD) and decreased thereafter. Plasma 20-S levels also increased with oocyte GVM in white bass, but were several-fold lower than DHP levels. Circulating E₂ and T levels were greatest during GVM and GVBD in both species and decreased to low levels during oocyte hydration and ovulation. Follicles from white perch and white bass which received a priming injection of hCG in vivo, produced both DHP and 20-S in vitro after exposure to hCG and their oocytes underwent GVBD. Ovarian incubates from unprimed fish of either species produced only E₂ and T and their oocytes did not complete GVBD. Oocytes from unprimed bass, but not perch, matured when follicles were exposed to hCG in vitro. Both trilostane and cycloheximide blocked in vitro production of DHP and 20-S and oocyte GVBD by white perch follices. DHP and 20-S were equipotent inducers of FOM in the GVBD bioassay. None of several other structurally-related steroids tested were effective within a physiological range of concentrations. These results indicate a role for DHP and 20-S in the control of FOM in white perch and white bass.     

Cardiac,ventilatory and metabolic responses of two ecologically dissimilar species of fish to waterborne cyanide

Changes in heart rate, ventilatory activity and oxygen consumption were determined in trout (Salmo gairdneri) and brown bullhead catfish (Ictalurus nebulosus) during exposure to a steadily increasing concentration of waterborne cyanide selected to produce death in 8–9 hours for each species. The lethal cyanide concentration for the bullheads was an order of magnitude higher than for trout. Trout developed an immediate and gradually increasing bradycardia throughout the exposure period. Cyanide produced tachycardia in the bullhead followed by a gradual onset of bradycardia as the concentration of cyanide was raised. Pericardial injection of atropine (a muscarinic cholinergic antagonist) indicated that bradycardia in the trout was due initially to increased vagal tone but later due to the direct effect of cyanide on the heart. Hyperventilation in the trout persisted throughout the exposure period, although the rate and amplitude fluctuated and was variable between individual fish. During the last hour of exposure (highest cyanide concentration), ventilation was characterized by rapid, shallow breaths followed by a sudden respiratory arrest. The bullheads exhibited hyperventilation during the first 3 hours of exposure followed by a gradual, linear drop in ventilation rate and amplitude until death occurred. Cardiac and ventilatory responses in both species were attributed to stimulation of central and peripheral chemoreceptors by cyanide. Evidence is presented which suggests the initial response in the bullheads was due, at least in part, to gustatory stimulation by the cyanide. Oxygen consumption of the trout remained above pre-exposure levels for the majority of the test period. Oxygen consumption in the bullhead paralleled the changes in heart and ventilatory rates. Whole-body lactate levels of fingerlings of both species during cyanide exposure were measured to estimate the extent of anaerobiosis. Whole-body lactate levels were much greater in the bullheads than the trout, indicating a higher capacity for anaerobiosis, possibly due to a greater fuel supply. Overall, the trout responded to cyanide in a manner similar to that produced by environmental hypoxia whereas the bullheads experienced a gustatory stimulus which masked the hypoxia-like response.     

An overview of stress physiology of fish transport: changes in water quality as a function of transport duration

This study brings an integrated analysis about the relationship between water deterioration and its physiological consequences in live fish transport. The analysis was focused on the transport water and its deterioration, and physiological challenges imposed on the fish. Usual commercial handling procedures employed to mitigate fish stress during transport were discussed. Future topics of research for the establishment of safer fish transport protocols were proposed. Transport was classified into short (≤8 h) or long transport (>8 h). The main issue in short transports should be the prevention of water pH reduction, while in long transports it is the increase in ammonia. Plasma cortisol is the most employed marker for stress and is acutely elevated upon short episodes of transport, but remains elevated even in long‐transport events. Plasma glucose is perhaps a better marker for handling stress. Plasma lactate, pH, osmolality CO₂ and ions should be more often evaluated. Plasma Na⁺ and Cl^‐ are very useful markers of acidosis, due to their respective exchange for H⁺ and , for acid–base regulation. The establishment of species‐specific transport protocols should be preceded by such combined analyses of water and physiological parameters.     

Are hatchery‐reared abalone naïve of predators? Comparing the behaviours of wild and hatchery‐reared northern abalone,Haliotis kamtschatkana (Jonas, 1845)

Abalone populations have declined worldwide, generating interest in enhancement using hatchery‐reared individuals. In many cases, such restoration efforts have met with limited success due to high predator‐induced mortality rates. Furthermore, the mortality rates of outplanted hatchery abalone are often considerably higher than for wild individuals. This study uses northern abalone (Haliotis kamtschatkana) as a case study to determine whether hatchery‐reared abalone behave differently than their wild counterparts. In the field, outplanted hatchery‐reared abalone were significantly less responsive than wild abalone, in terms of number of abalone responding and intensity of response, to nearby movement and to physical contact with an inert probe. Also, when encountering a cue to which all abalone responded (a seastar predator), hatchery‐reared individuals remained subdued. Anti‐predator behavioural deficits in hatchery‐reared abalone were more pronounced in 4‐year‐old individuals than in 1‐year‐old individuals, suggesting an influence of either age or amount of time spent in the hatchery environment. These behavioural differences are expected to increase the vulnerability of hatchery‐reared abalone to predators, and are likely a major cause of their elevated predator‐induced mortality when outplanted.     

Effects of cadmium on the kinetics of calcium uptake in developing tilapia larvae, Oreochromis mossambicus

The toxic effects of Cd²⁺ on Ca²⁺ influx kinetics in developing tilapia (Oreochromis mossambicus) larvae were evaluated. Addition of 20 µg l^-1 of Cd²⁺ to the environment of 0 and 3 day-old larvae competitively inhibited the Ca²⁺ uptake within 4h resulting in a great increase in K_m values for Ca²⁺ influx (19.3 and 17.4 fold, respectively) as compared with their respective controls. Consequently, the actual Ca²⁺ influx of larvae in solutions of 0.2 mM Ca²⁺ are suppressed by 32–45%. Also, 3 day-old larvae were more sensitive to internally accumulated Cd²⁺ than 0 day-old larvae. Although the Ca²⁺ influx in 0 and 3 day-old larvae may be restored to the levels of their respective controls with 24h of being transferred to a 20 µg l^-1 Cd²⁺ solution, total body Ca²⁺ content was significantly reduced in 3 day-old larvae. Increased Ca²⁺ uptake efficiency ensures sufficient Ca²⁺ for normal growth. However, rapid increase in Ca²⁺ influx after hatching also leads to higher Cd²⁺ uptake. Exposure to Cd²⁺ will lead to a drop in body Ca²⁺ content resulting in retardation of larval growth. Therefore, we conclude that if Ca²⁺ uptake is interfered with at this critical stage of development, larvae will not be able to maintain normal levels of body Ca²⁺ and will show signs of Cd²⁺ poisoning.     

Migratory dynamics of stream-spawning longnose gar (Lepisosteus osseus)

Abstract– Literature evidence suggests that lake-dwelling longnose gar (Lepisosteus osseus) enter tributary streams to spawn, Until the present study, the dynamics of this breeding migration had never been investigated quantitatively. During the summers of 1991 and 1992, longnose gar were captured as they entered Weaubleau Creek, Missouri, a tributary of Harry S. Truman Reservoir. The in-stream spawning migration began in early April and ended in late May, and was positively correlated with stream flow and water level, and negatively correlated with water temperature. In-stream residence times ranged from 15 to 94 days, with males exhibiting longer residence times than females. Once in-stream, longnose gar travelled as far as 10 km upstream and occupied certain pools at greater relative frequencies. Although the reason for this preferential utilization is not completely understood, it may relate to pool depth and riffle proximity. Longnose gar disperse from the spawning stream great distances, with gar captured in Weaubleau Creek being recaptured up to 48 km away. This information should provide fisheries biologists the means to consider the reproductive ecology of this species in their conservation and management decisions.     

美人鱼发光杆菌对凡纳滨对虾非特异性 免疫功能及抗病力的影响

在基础饲料中分别添加0.1%和1%美人鱼发光杆菌灭活菌、0.1%美人鱼发光杆菌活菌配制成3种免疫实验饲料,以基础饲料为空白对照组饲料,每组设3个平行样。对个体质量为(4.83±0.36)g的凡纳滨对虾进行为期20 d的饲养实验,分别在0、5、10、15和20d进行取样,以血清中的酚氧化酶(PO)、酸性磷酸酶(ACP)、碱性磷酸酶(AKP)、超氧化物歧化酶(SOD)和溶菌酶(UL)活性为免疫指标,探讨了美人鱼发光杆菌作为免疫制剂对凡纳滨对虾非特异性免疫效应的影响;在投喂免疫饲料后的第22天,按0.004 2 kg/kg体重的剂量,直接投喂对虾白斑综合征病毒(WSSV)病料,并记录累积死亡率。结果表明,美人鱼发光杆菌免疫实验组对凡纳滨对虾血清中PO、ACP、AKP、UL和SOD活性影响明显高于对照组,并且在饲料中添加美人鱼发光杆菌后,明显提高了对虾抵御WSSV感染的能力。其中0.1%美人鱼发光杆菌活菌实验组的抗病毒感染能力最强,WSSV感染14d内累计死亡率为63.3%±5.8%;而对照组为96.7%±3.3%。研究表明,美人鱼发光杆菌添加在对虾饲料中能提高凡纳滨对虾非特异性免疫水平,增强抵抗疾病的能力,将其作为对虾免疫增强剂具有良好的应用前景。