瓯江产唇(鱼骨)的早期形态发育研究

试验结果表明,受精卵授精后120 h,仔鱼开始出膜,初孵仔鱼(体长5.6~6.8 mm,平均体长6.35 mm)鱼体透明,体表和卵黄囊均无黑色素分布,尾鳍透明光滑,具口凹和眼色素并形成胸鳍原基,至卵黄被完全吸收时胸鳍鳍条开始形成,至28日龄时仔鱼各鳍发育完全,肌节数38~42。根据卵黄囊存在的情况和脊索的弯曲程度将仔鱼划分为卵黄囊仔鱼、前弯曲期仔鱼、弯曲期仔鱼、后弯曲期仔鱼。仔鱼眼径与头长比呈递减趋势,进入后弯曲期,体长迅速增加(≥11.8 mm)。唇鱼骨仔鱼体背与体侧黑色素由背鳍下方向尾部扩散,继而由中部至头部扩散。胸鳍附近最早出现鳞片,然后向后侧覆盖,最后在腹部出现鳞片。     

Early development and allometric growth patterns in burbot Lota lota L.

This study analyzed the morphological development and allometric growth patterns of Lota lota L. (burbot) larvae reared under controlled laboratory conditions. From hatching to day 50, twenty larvae were sampled each [between 1 and 14 days post-hatch (DPH)] or every second day (between 14 and 50 DPH) and measured under a stereoscopic microscope using analytic software. Based on the external morphology, the different stages during early development of burbot were identified: yolk sac larva 0–8 DPH [3.92–4.37 mm total length (TL)]; preflexion larva 9–26 DPH (4.57–12.06 mm TL); flexion larva (between notochord degradation and its replacement with rays) 28–34 DPH (14.00–16.34 mm TL) and postflexion larva/juvenile 36–50 DPH (18.20–29.27 mm TL). Allometric growth patterns of some parameters (e.g., total length, head length, body length, tail length, head depth, body depth, eye diameter) were modeled by a power function and described by the growth coefficient. Organogenesis and changes of body proportions in burbot larvae were more rapid and complex during the yolk sac and preflexion phase of development as larvae developed most of their sensorial, feeding, respiratory and swimming systems and after notochord flexion, when most morphological changes were related to the progressive transformation from pelagic larva to demersal larva/juvenile.     

Growth of juvenile chub mackerel Scomber japonicus in the western North Pacific Ocean: with application and validation of otolith daily increment formation

The growth of juvenile chub mackerel Scomber japonicus collected in the western North Pacific Ocean in 2007 and 2009 was examined based on the evidence of otolith daily increment formation in captive specimens. There was a significant difference in the relationship between known age and number of increments in the frontal and sagittal planes. Repeated markings on the otolith using Alizarin complexone and the coefficient of variation in number of increments suggest that the increments in the frontal plane of the otolith are more suitable for age estimation than those in the long and short axes of the sagittal plane. The increments in the frontal plane formed daily, and the first ring was usually deposited 3 days after hatch. Age of wild juveniles ranged from 24 to 211 days after hatch based on the frontal plane method. The estimated hatching periods of specimens ranged from February to June, but the April-hatched specimens were collected throughout the sampling periods of 2007 and 2009. The Gompertz growth model showed a difference in growth pattern in specimens between 2007 and 2009. The juveniles in 2009 appeared to grow more quickly than those in 2007 until summer, but thereafter the 2009 specimens seemed to grow more slowly.     

Early life history of yellow puffer,Chonerhinos naritus (Richardson, 1848) from Sarawak,Northwestern Borneo

The growth and morphological development including fins, spine distribution and pigmentation of larval and juvenile of hatchery‐reared yellow puffer, Chonerhinos naritus were described to provide essential information on the early life history of this species. The total length (TL) of newly hatched larvae was 3.42 ± 0.23 (mean ± SD) mm, reaching 5.66 ± 0.38 mm on 5 days after hatched (DAH), 7.80 ± 0.28 mm on 11 DAH, 9.88 ± 0.40 mm on 27 DAH and 10.92 ± 0.58 mm on 30 DAH. The yolk was completely absorbed in preflexion larvae at 4 DAH. The mouth opening started at 3 DAH of yolk sac larvae, while the teeth appeared starting from preflexion larvae at 7 DAH. Overall aggregate fin ray numbers including caudal fin attained full complement in postflexion larvae at 27 DAH. Several melanophores with appearance of small stellate were first appeared dorsally on the head of flexion larvae at 13 DAH, expanded at the dorsal region of the head, above the eye in juveniles at 30 DAH. The spines first appeared in preflexion larvae of C. naritus at 7 DAH, covering the ventral skin region below pectoral fin base and expanded to the ventral part of the body and nearly covered the whole abdomen region before the anus and below the eyes in juveniles. C. naritus remain as larvae for approximately 29 days, during which they metamorphose to the juvenile stage prior to sexual maturation. Observations in larvae development of C. naritus revealed similar characteristics with other Tetraodontidae species.     

Otolith microstructure of brown sole <Emphasis Type="Italic">Pseudopleuronectes herzensteini</Emphasis>: validation of daily ring formation and the occurrence of microstructure denoting metamorphosis

Brown sole Pseudopleuronectes herzensteini larvae and juveniles were reared to validate daily otolith ring formation. At 15°C, a check (a distinct ring) formed on the sagittae and lapilli at 6 days after hatching, and clear increments regularly formed outside the check. For both otoliths, the relationship between the number of days after hatching and number of increments was linear, and the slope of the line was approximately 1; therefore, daily formation was validated. At 12°C, the check formed on the lapillus 8 days after hatching. Accessory primordia (AP) began forming on the sagittae of metamorphosing larvae, and the shape of the sagittae became complicated. AP were not formed on the lapillus; concentric rings were formed throughout larval and juvenile stages. Wide and obscure increments formed on the lapilli during metamorphosis (metamorphosing zone, MZ). Based on MZ, concentric rings that have formed on the lapilli of juveniles can be separated into larval and juvenile rings. The morphs of large juveniles’ lapilli were bilaterally asymmetric, and the blind-side lapilli were most suitable for otolith microstructure analysis. This study provides fundamental information for otolith microstructure analysis in wild brown sole.     

Gonadal development in early life stages of <Emphasis Type="Italic">Spratelloides gracilis</Emphasis>

ABSTRACT:   The gonad of Spratelloides gracilis was not sexually differentiated in the yolk-sac, preflexion, flexion and postflexion stages. Sexual differentiation and development of the ovary and testis started in the transition stage from larva to juvenile. In juveniles at the fin ray completion stage, the ovary and testis could be distinguished because the ovary contained germ cells initiating meiosis and the testis had blood vessels and a high density of somatic cells. The ovary further developed in larger juveniles to have oocytes of perinucleolus stage together with those of the chromatin nucleolus stage, and oogonium. However, in the testis of larger juveniles, primary spermatogonium began proliferation by meiosis. Sexual differentiation may be regarded as one of morphological and functional changes accompanying metamorphosis in S. gracilis . Some fish larger than the mature size of 60 mm standard length had advanced germ cells and functional gonads, others did not have functional gonads. The distal end of the immature gonads did not connect with a genital duct near the anus. These observations indicate that S. gracilis has large variability in size-at-maturity. The variability in size-at-maturity in S. gracilis , together with large variability in age-at-maturity, may constitute an ecological basis for an extended spawning season in S. gracilis .     

Otolith development and daily increment formation in laboratory-reared larval and juvenile black-spot tuskfish <Emphasis Type="Italic">Choerodon schoenleinii</Emphasis>

Microstructures of lapilli were examined for reared larvae and juveniles of black-spot tuskfish Choerodon schoenleinii. Lapilli of larvae at 1 day after hatching have one diffuse and obscure ring with an otolith radius of 4.3 ± 0.50 μm (mean ± SD, N = 8). The slope and intercept of the regression between the number of days after hatching and increment counts did not differ significantly from one and zero, respectively, indicating that lapillus increments were formed on a daily basis after hatching. There was an ontogenetic shift in the relative values of somatic and otolith growth, which corresponded to the transition from pelagic larvae to settlement stage. Simultaneously, the daily increment width reached the maximum value. These findings suggest that age at maximum value of increment width can be used as an indicator of the planktonic larval duration while settlement mark is not found. Since ontogenetic shift in the relationship between otolith radius and body size was observed, back-calculation of somatic growth in black-spot tuskfish using the otolith radius during the early life stages should be analyzed with caution, and the method requires further validation.     

Early life history of the black anglerfish Lophius budegassa Spinola, 1807 in the Mediterranean Sea using otolith microstructure

The early life history of the black anglerfish, Lophius budegassa was investigated by otolith (lapilli) increment analysis. Samples of demersal juvenile L. budegassa ranging from 54 to 196 mm total length were collected during bottom trawl surveys in the central Adriatic Sea. By counting increments presumed to be deposited daily in the lapillar otoliths, 88 specimens of L. budegassa were successfully aged. Age estimates of juveniles ranged between 79 and 204 days, indicating that probably the pelagic phase of this species is relatively short and settlement occurs at less than 3 months of life. The analysis of check marks in the core area of lapilli enabled us to determine the period of endogenous feeding, which would last between 15 and 24 days after hatching. Back-calculated hatching dates and, consequently, the spawning season of L. budegassa in the Adriatic Sea was spread over a long period, lasting at least from February to June. The length at age relationship gave an estimate of mean growth rate of approximately 0.8–1.02 mm/day, indicating a faster growth rate of 0+ juveniles L. budegassa than previously thought. The implications of these findings on age estimates discrepancies between previous ageing studies on L. budegassa carried out using different calcified structure (sagittae or illicia) are discussed.     

Morphological development and growth patterns of the leopard grouper Mycteroperca rosacea during larval development

At 25 °C, metamorphosis in leopard grouper Mycteroperca rosacea larvae took 60 days after hatching. The total length at day 1 was 1.95±0.22 mm and juveniles reached a length of 30.64±0.23 mm at day 60; the increase was approximately linear. We describe eight stages of development during this period. Larvae with the yolk sac attached occur from days 1 to 4 (Stages 1 and 2). The preflexion occurs on days 5–20 (Stages 3 and 4). Bending notochord occurred at day 25 (Stage 5). The other morphological changes that precede the juvenile phase occurred progressively until day 60 (Stages 6–8). Allometric growth in the height and length of the head, trunk length, height and length of the tail and the diameter of the eye compared with the total length showed two distinct stages of growth. Inflexion point, where growth is positive, occurred when larvae reached between 18.75 and 21.59 mm, which corresponds to larvae at days 35–40.     

Effects of ontogeny, temperature, and light on vertical movements of larval Pacific cod (Gadus macrocephalus)

The role of behavior, especially vertical migration, is recognized as a critical component of realistic models of larval fish dispersion. Unfortunately, our understanding of these behaviors lags well behind our ability to construct three-dimensional flow-field models. Previous field studies of vertical behavior of larval Pacific cod ( Gadus macrocephalus ) were limited to small, preflexion stages (≤11 mm SL) in a narrow range of thermal conditions. To develop a more complete picture of larval behavior, we examined the effects of ontogeny, temperature, and light on vertical responses of larval Pacific cod in experimental columns. While eggs were strictly demersal, yolk-sac larvae displayed a strong surface orientation as early as 1 day post hatch (∼ 5 mm SL). Consistent with field observations, small preflexion larvae (<10 mm SL) showed no response to varying light levels. However, there was a direct effect of temperature on larval behavior: Pacific cod larvae exhibited a stronger surface orientation at 4°C than at 8°C. The behavior of larger, postflexion larvae (>15 mm SL) in experimental columns was consistent with a diel vertical migration and independent of water temperature: fish were more widely distributed in the column, and median positions were consistently deeper at higher light levels. These laboratory observations are combined with observations from discrete-depth (MOCNESS) sampling in the Gulf of Alaska to characterize the vertical distribution of larval Pacific cod and contrast ontogenetic patterns with walleye pollock ( Theragra chalcogramma ). The vertical movements of larval Pacific cod described here will be applied in the development of dispersal projections from Gulf of Alaska spawning grounds.     

Interannual variability in hatching period and early growth of juvenile walleye pollock, Theragra chalcogramma, in the Pacific coastal area of Hokkaido

Juvenile walleye pollock of the Japanese Pacific population were collected from the Funka Bay [spawning ground; 16–64 mm fork length (FL)] in spring and the Doto area (nursery ground; 70–146 mm FL) in summer. Hatch dates were estimated by subtracting the number of otolith daily increments from sampling dates, and their early growth was back‐calculated using otolith radius–somatic length relationships. Interannual change of the hatching period was observed during 2000–02, and the peaks ranged from mid‐February in 2000 to early‐April in 2002. In 2000, when a strong year class occurred, early life history of the surviving juveniles could be characterized by early hatching and slower growth in the larval stage (<22 mm length). Higher growth rate in 2001 and 2002 did not always lead to good survival and recruitment success. Even though their growth was slow in 2000, the larvae hatched early in the season had larger body size on a given date than faster‐growing larvae hatched in later season in 2001 and 2002. Bigger individuals at a certain moment may have advantage for survival. The delay of hatching period may result in higher size‐selective mortality, and as a necessary consequence, back‐calculated growth in 2001 and 2002 could shift towards higher growth rate, although abundance of such a year class would be at the lower level. Variability in spawning period, early growth and their interaction might have a strong relation to larval survival through cumulative predation pressure or ontogenetic changes in food availability.     

Morphological development of eggs, larvae and juveniles of laboratory-reared Ryukyu-ayu Plecoglossus altivelis ryukyuensis

ABSTRACT:   The development of embryos, larvae and juveniles of the Ryukyu-ayu, Plecoglossus altivelisryukyuensis are described based on laboratory-reared specimens.The eggs were spherical, 0.98–1.18 mm (mean 1.06 mm)in diameter with an adherent membrane. The incubation period after fertilizationwas approximately 155 h at a water temperature of 19.7–22.0°C(mean 20.7°C). Newly hatched larvae were 5.0–5.9 mm(mean 5.5 mm) in body length (BL) with 59–62 myotomes.Within 5 days after hatching, the larvae had attained 6.4–8.2 mm(mean 7.8 mm) BL and had completely consumed their yolk.Notochord flexion began at 13.7 mm BL and was completedby 16.3 mm BL. The rudimental dorsal, anal, pelvic andadipose fins appeared at 14.7, 16.3, 21.8 and 21.8 mm BL, respectively.All fin rays reached the same fixed number of adult fish at about28 mm BL. The comb-like teeth began to form at approximately30 mm BL and were fully developed at about 40–50 mm BL.The proportions of P. a. ryukyuensis specimens,which were consistent with adult fish, occurred at approximately40 mm BL.     

Critical swimming speed and maximum sustainable swimming speed of juvenile Pacific bluefin tuna, Thunnus orientalis

Tank wall collision is one of the major causes of mortality during the early-stage rearing of Pacific bluefin tuna, Thunnus orientalis (PBT). Therefore, to design a rearing environment that meets the needs of juvenile PBT, it is important to gather information about their swimming capabilities. We conducted experiments to examine the relative critical swimming speed (RCSS) and maximum sustainable swimming speed (MSSS) of early-stage PBT. The fish were kept in 3-tonne tanks and fed on artificial pellets every 2 h from dusk to dawn. We conducted two sets of experiments to measure swimming speed; the fish were introduced one at a time into a water funnel, and the water current velocity was gradually increased over time to estimate RCSS, or the water current was kept at a constant velocity to estimate MSSS. We measured the RCSS of 72 PBT juveniles (24–29 days after hatching (DAH); standard length (SL), 15.0 ± 2.3 mm) and the MSSS of 32 PBT juveniles (28–37 DAH; SL, 20.0 ± 5.1 mm) in the laboratory. The RCSS ranged from 4.7 to 20.3 SL/s (average, 12.4 ± 3.3 SL/s), and the MSSS was estimated to be approximately 4 SL/s. We speculate that introducing a water current in the rearing tank of no more than 4 SL/s could positively affect the survival of juvenile PBT.     

长江口凤鲚仔稚鱼不同发育阶段矢耳石生长

2014年4—8月于凤鲚(Coilia mystus)的主要繁殖期在长江口采集仔稚鱼103尾。分析凤鲚仔稚鱼样本得出日龄范围为5~48 d,体长为4.20~26.21 mm。为研究长江口凤鲚早期发育不同阶段生长,测定了凤鲚仔稚鱼(5~48日龄)体长随日龄的生长变化,其变化分为3个阶段(5~11日龄、12~30日龄、31~48日龄)。不同日龄阶段,体长的生长速率差异性显著(P0.05)。耳石早期发育研究发现耳石长、耳石宽随鱼体的生长而增长,在17~19日龄之后其生长速率增大约2倍。采用分段回归方法分析耳石长、耳石宽与日龄的关系,发现二者异速生长的拐点均出现在19~20日龄,拐点前为慢速生长,之后为快速生长。研究发现凤鲚早期生长发育阶段的耳石形态有较为显著的改变:卵黄囊期、前弯曲期为圆形;弯曲期耳石长的生长大于耳石宽的生长,耳石逐渐变成椭圆形;耳石变成稳定形态后,长宽比基本保持稳定。     

Development of digestive enzyme activity in spotted rose snapper,Lutjanus guttatus (Steindachner, 1869) larvae

We describe digestive enzyme activity during the larval development of spotted rose snapper, Lutjanus guttatus. Trypsin, chymotrypsin, leucine aminopeptidase, pepsin, amylase, lipase, and acid and alkaline phosphatase activities were evaluated using spectrophotometric techniques from hatching through 30 days. The spotted rose snapper larvae present the same pattern of digestive enzyme activity previously reported for other species in which pancreatic (i.e., trypsin, chymotrypsin, amylase, and lipase) and intestinal (i.e., acid and alkaline phosphatases and leucine aminopeptidase) enzymatic activities are present from hatching allowing the larvae to digest and absorb nutrients in the yolk-sac and live prey by the time of first feeding. The digestive and absorption capacity of the spotted rose snapper increases during the larval development. A significant increase in individual activity of all enzymes occurs at 20 DAH, and around 25 DAH, the juvenile-type of digestion is observed with the appearance of pepsin secreted by the stomach, suggesting that maturation of the digestive function occurs around 20–25 DAH. Our results are in agreement with a previous suggestion that early weaning may be possible from 20 DAH. However, the patterns of enzymatic activities reported in our study should be considered during the formulation of an artificial diet for early weaning of the spotted rose snapper.     

Improvement in the feeding activity, early growth and survival of Pacific bluefin tuna Thunnus orientalis larvae fed a casein peptide-based microdiet supplemented with inosine monophosphate

Two feeding experiments were conducted to determine the effect of a 5′-inosine monophosphate (IMP)-supplemented casein peptide-based microdiet (MD) on the feeding activity, growth and survival of Pacific bluefin tuna (PBT) larvae. PBT larvae [total length: 14.0 mm (Exp. 1) or 13.3 mm (Exp. 2)] were fed a casein peptide-based MD supplemented with or without 3% IMP for 12 days. As a negative control, a limited number of yolk-sac larvae of spangled emperor Lethrinus nebulosus were fed only for the first 7 days and starved for the next 5 days. A sufficient amount of yolk-sac larvae of spangled emperor was fed in the Exp. 2. All fish in the control group had died by 9 or 10 days after the experiment. Extensive mortality was observed in fish fed the MD. The MD was only found in the stomach contents of PBT fed the MD + IMP. Of the fish fed an IMP-supplemented diet, 50% survived for 12 days after the initiation of both feeding experiments. In addition, significantly higher growth than that observed during the first 7 days was seen in the PBT in the IMP treatment after 12 days of the feeding experiment. These results suggest that the supplementation of casein peptide-based MD with IMP could improve the feeding activity, survival and growth performance of PBT.     

Re-examination of age and growth of daggertooth pike conger Muraenesox cinereus in the western Seto Inland Sea, Japan

Age determination and growth using otolith rings in Muraenesox cinereus was re-examined in the western Seto Inland Sea, Japan. Previous study in this area indicated that new rings were formed annually from March to May, and then from September to October once individuals had achieved four or five rings. In this study, monthly changes in marginal growth rate indicated that the first ring was formed before November in the year following hatching, and from then on another ring was formed annually in July or August. The birth month was determined to be August based on a peak in monthly change in the gonad somatic index. Estimated von Bertalanffy growth functions were L = 806.6{1 ? exp[? 0.33(t + 0.06)]} and L = 1264.0{1 ? exp[? 0.19(t + 0.15)]} for males and females, respectively. Lengths after 3 years of age in this study were 100 mm longer than those in a previous study for both sexes.     

Embryonic and larval development of serpae tetra Hyphessobrycon eques (Steindachner, 1882)

In this study, the embryonic and larval development stages of one of the most important ornamental fish serpae tetra (Hyphessobrycon eques) are described. The early life stage is documented from fertilization until the beginning of the juvenile period. The fertilized eggs (the average diameter = 938.55 ± 35.20 µm) were incubated at a water temperature of 26 ± 0.5°C. The cleavage finished in 1:10 hr (=h) and the early blastula stage occurred at 1:26 hr post fertilization (hpf). The gastrulation started at 3:05 hpf, and 50% epiboly was observed at 3:25 hpf. Segmentation stage was monitored at 7:26 hpf. Embryonic developmental stage was completed and hatching occurred 20–21 hpf. The total length (TL) of newly hatched larvae was 2.64 ± 0.21 mm. The larval development of serpae tetra was divided into four different periods: Yolk‐sac larva (1–4 DAH, TL = 2.77 ± 0.09 mm ‐ 3.85 ± 0.11 mm), preflexion larva (5–12 DAH), flexion larva (13–15 DAH, TL = 5.78 ± 0.46 mm on the 15th day) and post‐flexion larva (16–30 DAH, TL = 10.7 ± 0.27 mm on the 28th–30th days). The mouth and anus are closed at 1 DAH. The mouth and anus opened at 4 DAH. Exogenous feeding started on the 4th day. The first gulping of the swim bladder was on days 3. The larva begins to swim freely, and the yolk sac was completely consumed at 4 DAH. Histological structures of the eye and brain of new hatched larva were clearly identified at 1 day after hatching (DAH). According to histological findings, the digestive system (stomach, intestine) started to develop and the liver could be seen on the ventral side of the swim bladder at 5 DAH. No histological difference was observed between the anterior intestine and the posterior intestine at 15–16 DAH. The larval metamorphosis was completed, and the larvae transformed into juveniles at 28–30 DAH.     

Development of sensory organs and changes of behavior in larvae of the sutchi catfish, <Emphasis Type="Italic">Pangasianodon hypophthalmus</Emphasis>

Larvae of the sutchi catfish Pangasianodon hypophthalmus hatch with morphologically immature features, but sensory organs develop rapidly as the fish grow. By 1 day old, yolk-sac larvae showed notochord flexion, and by 2 days old larvae were observed to have consumed a large part of the yolk sac. At this stage, larvae had well-developed eyes, olfactory organs with ciliated receptor cells, inner ears with semicircular canals, and numerous taste buds, and they commenced ingestion of rotifers, Artemia nauplii, and artificial compound feed. Two-day-old larvae had many free neuromasts on the surface of the head and flanks and clearly showed rheotaxis. By 20 days old, free neuromasts in postflexion larvae had sunk under the skin. At this later stage, larvae swam against a water current and schooled along the side of the fish tank. Rapid development of sensory organs and notochord flexion would be an adaptation for survival in conditions of flowing water, as in the Mekong River. In this study, we show that development of the lateral line in the postflexion stage seems to be closely related to larval behavior, suggesting that these developments could be essential for sutchi catfish larvae survival.     

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。