Larval development of the back keeled mullet Liza carinata

The sex ratio of the fish used in this study, was 1:1.5 females to males. Natural spawning of the keelback mullet, Liza carinata, in captivity was possible and occurred between December and February. The mean fertilized egg diameter of L. carinata was 0.8±.051 mm. Hatching took place after 36 h at 23°C. The mean total length of the just-hatched larvae was 2.0±0.179 mm. Larval developmental stages, growth, and morphological changes of L. carinata were described on the basis of a series of specimens (391 in total) reared from days 1 to 89 after hatching. Details of the larval developmental stages were drawn and photographed, with special reference being taken of morphological transformations. Larvae completed yolk absorption on the sixth day after hatching, and opened their mouths on day 4. Notochord flexion started on the sixteenth day at 5.0 mm total length. Transformation from larval to juvenile stage occurred between days 30 and 51 after hatching. The maximum size of larvae and the minimum size of juveniles which appeared during the transitional period were 19 and 9.9 mm TL, respectively. By day 51, all the larvae had changed into juveniles with a mean TL of 29.3±6.429 mm. The juveniles started to change into young adults with three anal spines by day 88 at a TL of 62 mm. This revised version was published online in September 2006 with corrections to the Cover Date.     

Influence of generation and photoperiod on larval development of Lobesia botrana (Lepidoptera: Tortricidae)

The influence of generation (under field conditions) and photoperiod (under laboratory conditions) on Lobesia botrana larvae development was studied. Some larvae were collected during three annual generations in two grape-growing areas of northeastern Italy, and others were individually reared in the laboratory from egg to pupa on an artificial diet under two different photoperiod conditions (respectively, daylight 16 h/d [long day {LD}] and 14 h/d [short day {SD}]). The mandible lengths of collected larvae were measured and the data analyzed morphometrically to determine the number of larval instars. In the laboratory study, the number of larval moultings, the mandible length of each instar, the development time from hatching larva to pupa, and the pupal weight were considered. The measurement of mandible lengths of larvae collected in the field indicated the existence of five larval instars in all three annual generations, but the size of the two oldest larval instars was significantly higher for third-generation larvae than for the previous generations. Under laboratory conditions, the larvae usually exhibited five instars, but the mandible lengths of larvae and the pupa size were greater for individuals reared under SD. These also took a greater number of days to develop from hatching larvae to pupae. Because a larger size of the final larval instar occurs in individuals that produce diapausing pupae under SD in both the laboratory and the field, a positive association between larval size and the probability of surviving the winter can be inferred.     

Laboratory culture of the larvae of Conus textile Linné (Gastropoda: Toxoglossa)

The larvae of the Indo-Pacific gastropod Conns textile Linné were reared in the laboratory from hatching through metamorphosis. Larvae fed a mixed phytoplankton culture of Isochrysis galbana and Phaeodactylum tricornutum grew at a rate of 0.06 mm/day and began metamorphosing 16 days after hatching. Unfed control cultures yielded no metamorphically competent larvae. Laboratory-reared larvae metamorphosed spontaneously on the walls of the fïberglass rearing tanks when their average shell length was 1.5 mm. Measurements made on field-collected Conns textile juveniles indicate that the larvae metamorphose at the same size in the laboratory as they do in nature.Rates of larval shell length increase and dry weight increase paralleled each other until metamorphosis. At this point, shell growth slowed while dry weight increased suddenly. It is suggested that this weight increase reflects calcification and strengthening of the fragile larval shell upon entering the benthic environment.     

Egg production, hatching rates, and abbreviated larval development of Campylonotus vagans Bate, 1888 (Crustacea: Decapoda: Caridea), in subantarctic waters

Early life history patterns were studied in the caridean shrimp, Campylonotus vagans Bate, 1888, from the subantarctic Beagle Channel (Tierra del Fuego). As a consequence of very large egg size (minimum 1.4 mm), fecundity was low, ranging from 83 to 608 eggs per female (carapace length [CL] 11-22.5 mm). Egg size increased continuously throughout embryonic development, reaching prior to hatching about 175% of the initial diameter. Due to low daily numbers of larval release, hatching of an egg batch lasted for about 2-3 weeks. The complete larval and early juvenile development was studied in laboratory cultures fed with Artemia sp. nauplii. At 7.0±0.5 °C, development from hatching to metamorphosis lasted for about 6 weeks. It comprised invariably two large zoeal stages and one decapodid, with mean stage durations of 12, 17, and 15 days, respectively. Larvae maintained without food survived on average for 18 days (maximum: 29 days), but did not reach the moult to the zoea II stage. Size increments at ecdysis were low in all larval stages (2.1-3.9%), indicating partial utilisation of internal energy reserves. A clearly higher increment (14%) was observed in the moult from the first to the second juvenile stage. Low fecundity, large size of eggs and larvae, an abbreviated mode of larval development, high larval survival rates during absence of food, demersal behaviour of the early life history stages, and an extended hatching period with low daily release rates are interpreted as adaptations to conditions typically prevailing in subantarctic regions, namely low temperatures (causing long durations of development) in combination with a pronounced seasonality in plankton production (i.e., short periods of food availability).     

A preliminary report on the development, growth and survival of laboratory reared larvae of the grey mullet, Mugil cephalus L.

Larvae from artificially bred grey mullet were reared in the laboratory and survival rates of 0.2 %, 5 % and 5 % achieved in three of six trials. Food consisted of wild zooplankton and Anemia nauplii. Feeding began on the fifth day, when the yolk sac was depleted, and intensified on the ninth day. The rate of yolk absorption and feeding intensity were reflected in the growth curve. Larval survival was not affected by withholding food from the larvae till the seventh day from hatching. Two critical periods associated with high larval mortality were apparent on the 2nd–3rd and 8th–11th days after hatching. These were preceded by an increase in specific gravity of larvae followed by passive sinking to the bottom of the rearing tank. Larval length increased from 2.63 mm at hatching to 17.69 mm at the end of the 42-day larval period. The larvae survived on benthic diatoms therefter. Maximum survival rates were achieved at 22°C. (Oceanic Institute Contribution No. 101).     

Vulnerability of larval white perch,Morone americana,to fish predation

Synopsis The vulnerability of white perch, Morone americana, larvae to yearling bluegill, Lepomis macrochira, predators was examined in relation to larval size, nutritional condition and relative abundance of alternative prey. Short-term (15 min) predation trials were conducted in 381 tanks in the laboratory. Larval vulnerability was measured as the proportion of larvae killed and the proportion of successful attacks per predator in each 15 min trial. No significant differences in vulnerability were apparent among larvae regardless of feeding history at sizes < 6 mm SL. At larval lengths > 6 mm SL, size of larvae was the crucial determinant of their vulnerability. Percentage of larvae killed in 15 min was nearly 100% at sizes < 6 mm SL, decreased to 30% at a length of 12.0 mm SL and dropped to 18% at 14.0 mm SL. Larvae initially feeding at low food levels for 2–4 d exhibited decreased growth of 13–25% over the first 3 wks of life, and simulations based on laboratory results indicated that these growth deficits could result in 5- to 68-fold decreases in survivorship at 38 days after hatching (DAH). The relative abundance of alternative prey also had a pronounced effect on mortality of larvae. A 10-fold increase in alternative prey (Daphnia magna) abundance decreased bluegill predation rates on white perch larvae by 10–20%, while a 100-fold increase in Daphnia density decreased larval mortality by 75–90%.     

Embryonic and larval development of a Japanese spinous loach,Cobitis takatsuensis

The embryonic and larval development ofCobitis takatsuensis, a mountain stream spinous loach, was surveyed by incubating artificially inseminated eggs. The mean diameter of the inflated eggs and mean total length of newly-hatched larvae were 2.7 mm and 5.7 mm, respectively. The eggs were spherical, transparent and unpigmented, with a pale yellow yolk and no oil globule. The daily cumulative temperature to hatching was estimated to be 70–110°C. day. Hatched larvae were unpigmented with outer gill filaments on their cheeks, as in otherCobitis species, but the melanophores were comparatively less obvious at each developmental stage. The larvae started feeding eleven days after hatching yolk absorption being completed sixteen days after hatching. All the fin rays were fully developed and the juvenile stage reached at 16 mm TL, 38 days after hatching. Embryonic and larval developmental traits ofC. takatsuensis, such as egg size, clutch size and larval pigmentation, were similar to the Korean species,Niwaella multifasciata, that lives in the upper reaches of the Nak-tong river, andN. delicata, which inhabits Japanese mountain streams, rather than to its congeners. Among cobitine fishes, the spawning of a small number of larger eggs yielding larger larvae without pigmentation, characteristics shared byC. takatsuensis, N. multifasciata andN. delicata, is attributable to adaptation to cold mountain streams.     

鲥鱼仔幼鱼食性与生长的初步研究

本文主要描述鲥鱼仔幼鱼阶段有关摄食、消化器官的发育、不同大小仔幼鱼食物组成特点、摄食量及其昼夜摄食节律。此外,还就仔幼鲥鱼人工饲养条件与天然状况下的生长作了比较。结果表明,只要供饵正常,孵化环道内生活的仔幼鲥生长速度可以略快于鄱阳湖同期天然生长个体的速度,为今后人工培育仔幼鲥进行放流和增殖提供资料。       

Nutritional condition and vertical distribution of Baltic cod larvae

Newly hatched Baltic cod Gadus morhua larvae are typically found at depths >60 m. This is a region of low light and prey availability, hence generating the hypothesis that larvae have to migrate from hatching depth to the surface layer to avoid starvation and improve their nutritional condition. To test this hypothesis, Baltic cod larvae were sampled during the spawning seasons of 1994 and 1995 with depth-resolving multiple opening/closing nets. Each larva was aged by otolith readings and its RNA/DNA ratio was determined as a measure of nutritional condition. The RNA/DNA ratios of these larvae aged 2-25 days (median 10 days) ranged from 0.4 to 6.2, corresponding to levels exhibited by starving and fast-growing larvae in laboratory calibration studies (starvation, protein growth rate, G_pi= -12.2% day⁻¹; fastgrowing larvae, G_pi=14.1%day⁻¹) respectively. Seventy per cent of the field caught larvae had RNA/DNA ratios between the mean values found for starving and fed laboratory larvae. Only larvae aged 8-11 days had higher mean RNA/DNA ratios above 45 m than below ( t -test, P<0.05). However, the instantaneous protein growth rates were significantly higher for all larval age groups in the surface layers ( t -test, P<0.05). Starving larvae were found in all depths sampled (10-85 m), whereas growing larvae (positive G_pi) were restricted to samples taken shallower than 45 m. These superior growth rates above 45 m corroborate the hypothesis and imply that migration to the shallow water layers is a prerequisite for good nutritional condition, growth and survival of Baltic cod larvae. The frequent occurrence of cod larvae older than 8 days in the deep water in poor condition suggests that a proportion of the larvae will die from Starvation in the deep layers of the Baltic Sea.     

Early ontogeny of Ancherythroculter nigrocauda and effects of delayed first feeding on larvae

Development of embryos and larvae in Ancherythroculter nigrocauda Yih et Woo (1964) and effects of delayed first feeding on larvae were observed after artificial fertilization. The fertilized eggs were incubated at an average temperature of 26.5°C (range: 25.7–27) and the larvae reared at temperatures ranging from 21.8 to 28°C. First cleavage was at 50 min, epiboly began at 7 h 5 min, heartbeat reached 72 per min at 24 h 40 min and hatching occurred at 43 h 15 min after insemination. Mean total length of newly hatched larvae was 4.04 ± 0.03 mm (n = 15). A one‐chambered gas bladder was observed at 70 h 50 min, two chambers occurred at 15 days, and scales appeared approximately 30 days after hatching. Larvae began to feed exogenously at day 4 post‐hatch at an average temperature of 24°C. Food deprivation resulted in a progressive atrophy of skeletal muscle fibres, deterioration of the larval digestive system and cessation of organ differentiation. Larval growth under food deprivation was significantly affected by the time of first exogenous feeding. Starved larvae began to shrink, with negative growth from day 6 post‐hatch. The point of no return (PNR) was reached at day 11 after hatching. Mortality of starved larvae increased sharply from day 12 after hatching.     

Verification of daily growth increment formation in saury otoliths by rearing larvae from hatching

Naturally spawned eggs of the Pacific saury,Cololabis saira, were collected in the field and reared in a tank to examine daily periodicity of growth increment formation in the otolith. Larvae were 6.9 mm in knob length at hatching. Their otoliths (sagittae) were 31 μm in radius and had 3–6 faint concentric rings. They started feeding within two days and grew at a rate of 1.1 mm/day on average through larval and juvenile stages feeding on rotifers,Artemia nauplii, and artificial diets. Otolith growth increments showed a concentric pattern with a distance of 3.5–5.0 μm between two adjacent increments. The number of growth increments was almost equal to a known age in days plus 4 or 5. A regression line of number of increments (N) on known age in days (D) between 0–30 days after hatching was N = 4.81 + 1.01D, which shows that one increment was deposited per day.     

Influence of egg size on embryos and larvae of Fundulus heteroclitus (L.)

Egg size for Fundulus heteroclitus (L.) populations is concordant with the distribution of the two F . heteroclitus subspecies, i.e. F. h. heteroclitus eggs are considerably larger than F. h. macrolepidotus eggs. The influence of egg size on survival of embryos during incubation and survival and growth of newly-hatched larvae was estimated for four populations representing both subspecies along the Atlantic coast of the United States and in Delaware Bay. Survival of embryos was determined for incubation periods of 14, 21 and 28 days. Greatest differences in survival were detected following the longest incubation period where less than 50 per cent of the smaller F. h. macrolepidotus eggs survived while little or no mortality was detected among the larger F. h. heteroclitus eggs . Influence of egg size on larval survival was also greatest among those larvae hatched after 28 days where F. h. macrolepidotus larvae survived without food, for an average of 6 days, while F. h. heteroclitus larvae survived 11–12 days. F. h. heteroclitus larvae were significantly larger at hatching than F. h. macrolepidotus larvae. Larval growth rates were the same (0.4 mm day⁻¹) in both subspecies. As a result, size differences at hatching were still maintained after 42 days of growth. The differences in egg size along with other morphological and reproductive characteristics of F. heteroclitus populations probably represent genetically based adaptations to environmental conditions, of which the length of the spawning season is one of the major components stimulating the coevolution of these traits.     

裸项栉鰕虎鱼的全人工繁殖及其胚胎发育

目的研究裸项栉鰕虎鱼全人工繁殖及胚胎发育,为该鱼的实验动物化研究奠定基础。方法对胚胎和仔稚幼鱼各个发育期的连续取样,系统地观察了裸项栉鰕虎鱼各发育期的形态变化及生长特征。结果水温25．8℃～26．5℃,裸项栉鰕虎鱼受精后约82h仔鱼开始出膜,初孵仔鱼全长1．42～1．73mm,1d开口摄食,3d卵黄囊消失,23d第一背鳍形成,鳞片出现;33d全身被鳞;初孵仔鱼经97d发育成熟,繁殖周期约为36d;雌鱼性腺成熟系数可达40％,个体相对生殖力达每克8193．5粒。结论裸项栉鰕虎鱼具有个体小、性成熟早、生殖季节长、繁殖周期短、繁殖力强等特点,可进行室内规模化人工繁殖和培育。     

Development of eggs,larvae and juveniles of the puffer,Takifugu chrysops,reared in the laboratory

The artificial fertilization of the puffer,Takifugu chrysops (Hilgendorf), was carried out at Sajima in Yokosuka City on May 22, 1984. Hatched larvae were reared for a period of about 150 days. The spawning period seems to extend from mid to late May in the eastern part of Sagami Bay. The eggs were spherical, pale milky white and semitransparent, demersal and adhesive in nature, measuring 1.32±0.04 mm in diamter, and with a cluster of small oil-globules. The incubation period was about 162 hours at a water temperature of 17.4 to 21.8°C. During embryonic development, the only pigment cells that appeared on the embryo were the black chromatophores. The newly hatched larvae measured from 2.72 to 3.06 mm TL, averaging 2.87±0.1 mm TL, and 22–23 (9 + 13?14) myomeres. At yolk absorption, 4 days after hatching, the larvae attained 3.64–3.79 mm TL. On the 11th day, postlarvae averaged 4.69±0.24 mm TL. Larval finfolds disappeared and rudimental dorsal, anal and caudal fins were formed. There were two large clusters of melanophores, one on the back, exteding from the mid-base of the dorsal fin to the caudal peduncle region, the other along the anal fin base. The color of the body began to turn pale green to brownish-orange and spinelike scales appeared on the belly. Eighteen days after hatching (7.02±0.27 mm TL), the caudal notochord began to turn up and a “constriction” appeared on the posterior margin of the caudal fin membrane. This notch moved upwards as the notochord upturning advances. The larvae attained full fin ray counts and reached the juvenile stage at 9.1-9.5 mm TL, 24 days after hatching. Characteristic black blotches on the back and specific brownish orange body color appeared at the stage of 20 mm TL, 24 days after hatching. The growth during the larval stage and early juvenile stage (24 to 51 days after hatching) were expressed by the following equations, wherey is total length (mm) andx is days after hatching.y ₁=2.8424× 1.0509⁹ (0≦x≦24)y ₂ = 3.7872×1.0372^x (24≦x≦51)     

Larval development,growth and age determination in the sharpnose pufferfishCanthigaster valentini (Teleostei: Tetraodontidae)

The eggs, early larvae and juveniles of the sharpnose pufferfishCanthigaster valentini are described, based on material collected in Great Barrier Reef waters. Eggs were obtained in the field by divers and reared in the laboratory. The eggs are spherical, strongly adhesive, 0.68–0.72 mm in diameter, possess a dense cluster of small oil droplets, and hatch around sunset 3 to 5 days after fertilization. Newly hatched larvae have a small yolk sac, pectoral fin folds, 17 myomeres (6 pre-anal, 11 post-anal) and measure 1.30–1.40 mm in notochord (standard) length. The eggs ofC. valentini differ from those of other tetraodontids in being much smaller and having a longer incubation time. The larvae can be distinguished from other tetraodontid larvae by pigmentation, myomere count and size at hatching. Growth is most rapid during the first day of larval life. Age determinations (based on otolith microstructure) of field collected juveniles, both pelagic and newly settled, indicate a pelagic phase of between 64 and 113 days for this species. This estimate appears consistent with the extended pelagic juvenile stages observed in other tetraodontiform fishes and could indicate thatC. valentini can delay settlement for some time after becoming competent to settle at a minimum age of 64 days.     

Growth and morphological development of laboratory-reared larval and juvenile Pangasianodon hypophthalmus

The morphological development, including the fins, body proportions and pigmentation, of laboratory-reared larval and juvenile Pangasianodon hypophthalmus was described and their behavioral features were observed under rearing conditions. Body lengths (BL) of larvae and juveniles were 3.0 ± 0.2 (mean ± SD) mm just after hatching, and 12.9 ± 1.1 mm on day 13, reaching 23.4 ± 1.8 mm on day 25 after hatching. Aggregate fin ray numbers (for caudal fin, principal soft ray number) attained their full complements in specimens larger than 12.8 mm BL. Notochord flexion began in yolksac larvae on day 0 (10.5 h after hatching), with teeth buds and barbels appearing with jaw formation in yolksac flexion larvae on day 1. Melanophores on the body increased with growth, with a broad vertical band forming on the lateral line and an oblique band extending from above the pectoral fin base towards the forepart of the anal fin during the postflexion larval and juvenile stages. Body proportions became relatively constant in juveniles, except for maxillary barbel length (MBL), which continued to decrease. Yolksac flexion larvae started feeding on day 2 with the onset of intense cannibalism. Yolks were completely absorbed by day 3, and cannibalism ended by day 6. Subsequently, fish displayed a schooling behavior with growth, preferring relatively dark areas during the juvenile stage.     

Effect of delayed metamorphosis on larval competence, and post-larval survival and growth, in the abalone Haliotis iris Gmelin

Marine invertebrate species vary in their ability to delay metamorphosis, and in the degree to which delayed metamorphosis compromises juvenile performance. Abalone (Haliotis iris) larvae were deprived of metamorphosis cues and the effects of delayed metamorphosis on larval competence, and post-larval growth and survival were quantified. Larvae were exposed to a metamorphosis inducer (the coralline alga Phymatolithon repandum (Foslie) Wilks and Woelkerling) on Days 11, 18, 22, 26, 30 and 34 post-fertilisation (temperature 16-17 degrees C). Post-larvae were reared on diatoms (Nitzschia longissima Grunow) for 3-4 weeks post-metamorphosis. Delayed metamorphosis caused progressive negative effects on post-larval performance. Virtually all larvae initiated metamorphosis in response to P. repandum, regardless of larval age. The proportion of post-larvae that developed post-larval shell growth within 2 days of metamorphosis induction dropped only approximately 20% from Day 11 to Day 26 (P>0.05), but was significantly lower by Day 30 and Day 34 (P<0.001). Larvae that metamorphosed on Days 11, 18 and 22 showed high survival (>80%) and growth rates (means of 20-22 μm shell length per day). In contrast, larvae that metamorphosed on Day 26 and Day 30 had poor survival (30-40%) and lower (P<0.05) growth rates (15-16 μm/day). Of the larvae that metamorphosed on Day 34, only 7 (30%) survived their first week post-metamorphosis, and they grew only 2 μm/day on average. Only one of these post-larvae (4%) survived the second week. The visible yolk supply diminished over the life of the larvae and was near zero by Day 34. Nearly all larvae had died by Day 38. H. iris larvae remained competent to metamorphose for at least 3 weeks after they attained competence. Post-larval growth and survival were not reduced if metamorphosis occurred within 3 weeks of fertilisation. This extended period of larval competence implies that H. iris larvae can potentially disperse for up to several weeks before successful metamorphosis.     

The life-history strategy of deepwater sculpin, Myoxocephalus thompsoni (Girard), in Lake Michigan: dispersal and settlement patterns during the first year of life

Deepwater sculpin, Myoxocephalus thompsoni (Girard), were sampled from six stations from the 15–100 m depth contours in Lake Michigan between April 1983 and July 1984. In south-eastern Lake Michigan M. thompsoni lay benthic eggs in offshore waters, which hatch between November and August, with peak hatching in March. Abundance of larvae in pelagic samples was higher offshore than inshore, but larval size was greater and development more advanced at inshore stations, indicating an inshore movement after hatching. Larvae reached metamorphosis at 20 mm and settled to the bottom beginning in July. Pelagic larvae 20–40 mm were found in the lower water column at all stations, but newly settled individuals were only captured with bottom trawls at inshore locations (≤60 m depth). Data from ichthyoplankton and bottom trawl samples in 1983 and 1984 indicated that locations for successful settlement of larvae to the bottom extended only as deep as the shallowest fringe of the adult population (> 50 m in 1983). In 1983, maximum density of larvae reached 0.4 individuals m⁻³ by June. Survival from the pelagic larval stage to the demersal young-of-year stage in 1983/1984 was c . 0.1–0.4%. The specific mechanism of mortality at the time of transition to a demersal habit has not been determined.     

Use of granulated fertilizers with Actellic EC 50 insecticide in the control of mosquito larvae

Granulated fertilizers [ammonium nitrate, synthetic fertilizer] were used as carriers to prepare an insecticide granulate suitable for the control of Aedes cantans and Aedes vexans mosquito larvae under field conditions. The insecticide granulate was obtained by mixing 1 volume unit of Actellic EC 50 with 50 volume units of fertilizer. The optimal dose required to ensure and effective control of Aedes mosquito larvae was 2--5 g of granulate per 1 m3 of water [i.e. 2--5 kg/ha per each 1- cm depth of water] in hatching areas with a relatively clean water or during periods of slow larval growth and development, and 10 g of granulate per 1 m3 of water for hatching places polluted with organic substances or for periods of accelerated larval growth during summer months. The described Actellic EC 50 application practice ensures a complete survival of numerous non-target water organisms, including Tubifex species, Rhynchelmis species, molluscs, flatworms [Turbellaria], Asellus aquaticus, water mites [Hydrachna sp.] water striders (Gerris lacustris] and Dixella species larvae].