Embryonic and morphological development of larvae and juveniles of the Amberjack,Seriola dumerili

Embryonic and morphological development of larvae and juveniles of the amberjack,Seriola dumerili Risso, are described using specimens raised at Yaeyama Station (Ishigaki Island, Okinawa Pref.), Japan Sea Farming Association. The specimens obtained from brood fish (3 females, 3 males) were treated with gonadotropin and spawned on 6th of April 1987. The eggs of amberjack are pelagic, spherical in shape and 1.01–1.17 mm in diameter. The yolk is roughly segmented and has a single oil globule 0.22–0.24 mm in diameter. The perivitelline space is narrow. During development, a few melanophores and no xanthophores were observed on yolk. Hatching took place 35 hrs. 15 min. after spawning out at temperatures 23.1–23.7°C. The newly hatched larvae were 2.84–3.04mm in TL with 27 (13+14) myomeres and an oil globule anteriorly situated beyond the head. 3 days after hatching 4.00 mm TL, the mouth opened. 10 days after hatching 4.26 mm TL, small denticles appeared on the margin of the upper jaw and there were 1 anterior and 2 posterior preopecular spines. At 5.96mm TL, notochord was slightly flexed. Caudal, dorsal and anal fins with rudiments of rays appeared at 8.00 mm TL. The specific numbers of all fin rays and spines were obtained in a juvenile 9.60 mm TL. In a juvenile 34.25 mm TL, 54 days after hatching, the characteristic brown band of amberjack had appeared on head. Some notable changes in relative growth were observed at 5 mm and 15 mm in TL.     

Spawning behavior and early life history of the sharpnose puffer,Canthigaster rivulata,in the aquarium

Specimens ofCanthigaster rivulata (Temminck et Schlegel) were collected from Kominato and Hayama, central Japan, from May, 1985 to October, 1986. On the basis of the gonadosomatic index, gonadal histology and results of artificial fertilization of these specimens, the spawning season is considered to extend from late June to mid-September. The specimens exhibited the following dimorphic differences associated with sex: 1) The male is larger than the female. 2) Ventral side of the body is brownish orange in the male with vermiculated or reticulated patterns of bright violet, while it is white in the female. 3) The male has a well-developed skin fold along the mid-dorsal and mid-ventral lines, which is greatly elevated during courtship; whereas the female’s skin folds are not or slightly developed and conspicuous only during courtship. In an aquarium with the water temperatures of 22 to 26°C, a pair of fish spawned every four days late in the morning for three consecutive months. Courtship and spawning occurred in a pair. The male swam in front of the female, and elevated the skin folds both dorsally and ventrally, fully spreading the unpaired fins, with the ventral side of the body flashing bright blue and the dorsal side turning dark. Both fish swam in a circular fashion, elevating the skin folds. The male followed the female nudging her abdomen with his snout. Both fish turned upward, and released gametes. The eggs are spherical, 0.53–0.73 mm in diameter, demersal, adhesive, transparent, and pale yellowish orange in color, and contain a cross-shaped or asteroid cluster of oil globules. The egg membrane was thick and consisted of about 14 concentric layers. The incubation period ranged from 73.5 hours at 28.2–28.5°C to 145.0 hours at 22.1–22.4°C. The newly hatched larvae were 1.38–1.98 mm in total length (TL) with 84-11-13 = 19–21 myomeres. The yolk was absorbed when the larvae attained 1.49–2.22 mm TL, three days after hatching. The larvae were fed on oyster larvae, blue mussel larvae, sea-urchin larvae and rotifers, but all of them died in 16 days. During the embryonic and early larval stages, the only pigment cells that appeared on the body were the black chromatophores.     

Development of the eggs and larvae of the pike eel,Muraenesox cinereus

Embryonic and larval development of the pike eel,Muraenesox cinereus, are described following natural fertilization in the laboratory. Eggs are pelagic and spherical with diameters from 1.8 to 2.1 mm and have a colorless, transparent chorion and numerous oil globules. Hatching occurs 36 hours after spawning at a water temperature of 25°C. Newly-hatched larvae are 5.8 mm in mean TL, and the number of myomeres averages 86. Absorption of the yolk is completed 8 days after hatching, at 9–10 mm TL. Larvae survive for 10 days without food supply. At this time they are 11.2 mm in mean TL and have 97 + 55=152 myomeres, which is a diagnostic character of this species. They have large eyes and well-developed jaws with sharp teeth.     

Early development of the laboratory-reared flounder,Pleuronichthys cornutus

Fertilized eggs ofPleuronichthys cornutus were obtained by both artificial fertilization and natural spawning of laboratory-reared fish. The present paper describes in detail the early development of the fish and the rearing methods employed to provide basic information for mass production of this species. Eggs and sperm for artificial fertilization were obtained from adult fish caught in the Ariake Sound, Kyushu in November and December of 1984. Their maturation was successfully induced by intermuscular injection of pituitary homogenate of the silver carp,Hypophthalmichthys molitrix. Fertilized eggs were also obtained in 1985 by natural spawning of a broodstock kept in a tank for a year. Hatched larvae were fed successively with rotifers,Artemia nauplii and the harpacticoid copepod,Tigriopus japonicus and reared for 80 days. Ten thousand young fish of about 33 mm TL were obtained in 1984 and 1985 with the survival rate of about 17%. Ten developmental stages were defined on the basis of the morphological characteristics: A) newly hatched to 4 day old larvae, 2.7 to 4.1 mm TL (2.6 to 3.9 mmNL), yolk sac present; B) 4 to 16 day old larvae, 3.8 to 5.9 mm (3.6 to 5.6 mm), yolk resorbed, actively feeding on rotifers; C) 15 to 30 day old larvae, 6.3 to 8.3 mm (6.0 to 7.9 mm), notochord straight, hypural fin ray visible; D) 24 to 40 day old larvae, 6.7 to 9.2 mm (6.4 to 8.8 mm), caudal notochord upturned (45°); E) 28 to 45 day old larvae, 7.9 to 10.8 mm (7.5 to 10.3 mm), caudal notochord upturned (45°–90°); F) 32 to 50 day old larvae, 10.8 to 15.7 mm (8.8 to 12.8 mm BL), eyes symmetrical; G) 35 to 66 day old larvae, 13.4 to 20.0 mm (10.9 to 16.3 mm), eyes asymmetrical, but left eye not visible from the right side; H) 40 to 75 day old larvae, 13.8 to 26.2 mm (11.3 to 21.4 mm), the upper edge of left eye visible over top of the head from the right side; I) 46 to 89 day old larvae, 20.1 to 27.4 mm (16.4 to 22.4mm), left eye on the edge of the head and pupil visible from the right side; and J) juveniles of 51 day old or over, 23.6 mm or more (19.3 mm or more), metamorphosis completed. One to three inflections were found for relative growth of total length, eye diameter, upper jaw length, preanal length, and distance between the base of the pectoral fin and the anus against the notochord length or body length. Two inflections were found for body length (or notochord length)-body weight relationship. Most inflections appeared at the stages of D, F and J, corresponding to the body length of 8, 9–12 and 18–22 mm respectively.     

Induction of ovarian maturation and development of eggs,larvae and juveniles of the tonguefish,Cynoglossus abbreviates,reared in the laboratory

Cynoglossus abbreviatus spawns from mid-March to mid-April in the Sea of Shimabara in Kyushu. During the spawning season ovarian maturation was successfully induced by injection of the pituitary homogenate ofHypophthalmichthys molitrix. The dose of the aceton-dried pituitary homogenate was 6.5 mg/kg body weight ofC. abbreviatus. It took about 2 days for ovulation after injection at a water temperature of 14 to 16°C. Artificial fertilizations were accomplished on March 29, 1974 and again on April 7, 1984, using the females matured by hormone injection in the latter case only. The larvae were reared on the rotifers,Artemia nauplii,Tigriopus japonicus and copepods collected from the sea over a period of 113 days in 1974 and 58 days in 1984. The eggs were pelagic, spherical, 1.19–1.23 mm in diameter and had 30–50 oilglobules of 0.068–0.095 mm in diameter, and the perivitelline space was narrow. The incubation period was 90–98 hours at a water temperature of 14 to 16°C. The newly hatched larvae were 3.18–3.45 mm TL and had 61–64 myomeres. The larvae had many melanophores and xanthophores on the body, forming three bands on the caudal region, but were lacking chromatophores on the finfolds. The yolk was completely absorbed when the larvae attained a size of 4.7–5.6 mm TL 8 days after hatching. A single elongated dosai fin ray developed on the head in the 8-day old larvae. The ray was reduced in size as long as the other rays 1 or 2 days after metamorphosis. The rudiment of pectoral fins were found on the both sides of the body in the 2-day old larvae, but two of them disappeared after metamorphosis. A pelvic fin first appeared as a ventral bud just anterior to the gut in the larva of 8.39 mm TL. The full count of 4 rays was observed on the larva of 10.83 mm TL. Metamorphosis began 22 days after hatching when the larvae were 11.20 mm TL. The right eye began to shift the left side of the head at night and reached to the final place after 8.5 hours. It took about 36 hours to complete the metamorphosis, including the eye movement and fusion of the hole in the rostral beak. At the last stage of metamorphosis, the dosal, caudal, anal and ventral fins became confluent. The larvae reached the juvenile stage at a size of 13.5–14.0 mm TL, approximately 28 days after hatchling. The growth of larvae reared in 1974 is expressed by the following equations: Y₁ = 3.448 · 1.0507^x (8≦X≦28) Y₂ = 6.3322 · 1.0275^x (28≦X≦75) where Y is the total length (mm) and X is the number of days after hatching. Growth rate changed after metamorphosis.     

Reproduction and development of the weakly electric fish,Pollimyrus isidori (Mormyridae,Teleostei) in captivity

Synopsis No clear sexual dimorphism occurs in Pollimyrus isidori. Females usually grew slightly larger than males. The anal-fin reflex, however, makes it easy to discriminate between males and females. Spawning took place during the first six hours of the dark phase, in the territory of the male. During each spawning act 2–4 eggs were laid. The male put the eggs into a well-hidden nest previously constructed from plant material. The eggs, free embryos, and larvae of several spawnings were guarded by the male for several weeks. The females laid on average 120 eggs per fractional spawning. The eggs were 2 mm in diameter, not adhesive and very yolky. There was a relationship between pH and viability (% embryos hatched). Hatching occurred on the third day after spawning. The respiratory network of segmental origin in the median fin fold was well developed in the free embryos. Transition to exogenous feeding occurred on day 14. The larval period ended when the fish were 15 mm long and 40–50 days old. First gonadal recrudescence occurred at a total length of 6 cm (about 200 days old). The environmental factors decreasing conductivity and pH, increasing water level, and imitation of rain led to gonadal recrudescence, but pH did not act as a cue. Recrudescence was triggered by a decrease of conductivity, but absolute values or ionic composition of the water were not important. Maturation was completed after about fifty days. Mature and spawning fish no longer required any variation of these environmental factors to maintain mature gonads. A steady and considerable increase in conductivity led to gonadal regression. The fish did not show postbreeding refractoriness.     

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.     

Early ontogeny of coal grunter from hormone-induced spawnings and laboratory-reared embryos and larvae

Spawning of coal grunter Hephaestus carbo was successfully induced using doses of human chorionic gonadotrophin (hCG) between 500 and 3000 IU kg (body weight)⁻¹. Water hardened eggs are telolecithal, amber in colour, spherical, transparent, demersal and slightly adhesive with a single large oil droplet and perivitelline space 47% of total egg volume. Cleavage begins 10–15 min after fertilization. Epiboly begins 6h after fertilization and continues for 4 h. Invagination of the neural tube is apparent 11·5 h after fertilization, followed by progressive organogenesis up to hatching 60–80 h after fertilization. An invagination in the yolk, consistent in shape, position and time of appearance among embryos spawned from numerous brood stock pairs, was visible in all fertilized eggs between neurulation (11-5 h) and early organogenesis (20 h). The functional significance of this yolk invagination is unknown. Newly-hatched larvae (4·2 mm L _T) are elongate and possess well developed eyes, a functional mouth, and a large yolk sac. Yolk is fully resorbed and first feeding occurs at 6 days posthatching. The sequence of fin formation is caudal, second dorsal and anal, first dorsal, pectoral and pelvic. The prefiexion larval stage lasts for c. 8 days and flexion of the notochord is complete within a further 8–9 days. Squamation commences at 30 days posthatching and transition to the juvenile life stage is complete by 35–40 days posthatching.     

Spawning, egg development and early ontogenesis in rock cod Patagonotothen ramsayi (Regan, 1913) caught on the Patagonian Shelf and maintained in captivity

Rock cod Patagonotothen ramsayi (Regan, 1913) is one of the most abundant fish of the family Nototheniidae inhabiting the Patagonian Shelf and upper Slope in the southwest Atlantic. Recently, P. ramsayi became an important commercial species around the Falkland Islands with annual catch of 60,000–75,000 t. The present study aimed to reveal previously unknown aspects of reproductive biology of P. ramsayi during the first successful maintenance of adults for more than a year in an aquaculture facility with running seawater. The fish spawned at the end of austral winter. During spawning, males changed their coloration dramatically, occupied artificial shelters on the bottom and showed aggressive territorial behaviour. Egg masses were light-yellow to light-orange irregular spongiform. They were negatively buoyant, but located outside shelters and were ignored by males. Egg diameters varied between 2.1 and 2.3 mm, and the number of eggs per egg mass ranged from 26,800 to 123,400. Embryogenesis lasted 28–32 days. Total lengths of newly hatched larvae ranged from 6.2 to 6.7 mm. The yolk sac feeding period lasted approximately 11 days, during which the larvae showed negative phototaxis. One-month-old larvae attained 8.8–9.0 mm in length. This study confirms that P. ramsayi exhibit the reproductive strategy typical for nototheniid species occupying low-latitude peripheries of their distributional range, characterised by a combination of r-features (small eggs and larvae, high fecundity) and K-features (territorial behaviour and possible nest guarding).     

Development of eggs,larvae and juveniles of the labrid fish,Halichoeres poecilopterus,reared in the laboratory

Embryonic, larval and juvenile development of the labrid fish,Halichoeres poecilopterus, is described using a laboratory-reared series. The eggs, measuring 0.60–0.72 mm in diameter, were pelagic and spherical with a single oil globule (0.12–0.16 mm in diameter). Hatching occurred 18 h 48 min after spawning. The newly-hatched larvae, measuring 1.46–1.70 mm TL, had 8–114 + 16–18 myomeres. A conspicuous melanophore appeared on the dorsal finfold 8 h after hatching, at ca. 2 mm TL. The yolk was completely absorbed 3 days after hatching, at 2.52–2.72 mm TL. Flexion of the notochord started at ca. 6 mm TL and was finished at ca. 8 mm TL. Aggregate numbers of all fin rays were completed at ca. 14 mm TL. Squamation was almost completed at ca. 20 mm TL.     

Reproductive biology and larval morphology of the marine plotosid Cnidoglanis macrocephalus (Teleostei) in a seasonally closed Australian estuary

Monthly trends shown by gonadosomatic indices, the prevalence of the different gonadal stages, and the size distribution of the oocytes, indicate that the large marine and commercially important plotosid Cnidoglanis macrocephalus spawns in Wilson Inlet between October and January. The conclusion that spawning occurs within this seasonally closed estuary was confirmed by the presence of males in large nests and by the capture of newly-hatched, yolk sac larvae from one of those nests. The fact that C. macrocephalus, which is also widely distributed in coastal marine waters throughout much of southern Australia, can spawn within Wilson Inlet would be of particular value to this species in those periods when closure of the estuary would preclude a seawards spawning migration. Sexual maturity is size dependent, with spawning rarely occurring before fish have reached a total length of 425 mm. Sexual maturity was attained by a few fish at the end of their second year, by several at the end of their third year and by most, if not all fish, at the end of their fourth year. Comparisons with data for the more northern and permanently open Swan Estuary indicate that C. macrocephalus also spawns within that system and that the spawning time of this species is related to water temperature. The adult male guards the larvae under its pelvic fins in burrows. The larvae increased in total length from 29 mm just after hatching to 43 mm in the 17–18 days after capture, during which time their yolk sac was resorbed. Details are given of the morphology, morphometrics, meristics and pigmentation of larval C. macrocephalus. In comparison with the larvae of three other plotosid genera, the larva of C. macrocephalus is far larger in size and more developed at hatching and takes a shorter time to transform into a juvenile.     

Embryonic and early larval development of <Emphasis Type="Italic">Cottus czerskii</Emphasis> Berg, 1913 (Scorpaeniformes: Cottidae)

The embryonic and early larval development of the Cherskii’s sculpin Cottus czerskii Berg, 1913 was studied. The duration of the embryonic period was 21 days at a water temperature of 9–10°C. Pelagic larvae of approximately 8.0 mm total length leave the egg envelopes, with a large rounded yolk sac with one large oil globule, 10–12 trunk and 30–31 precaudal myomeres and several large melanophores on the yolk sac, 2 melanophores in the peritoneal region, and 30 melanophores in a postanal ventral row. At 11 days after hatching at a length of 9.0 mm, the yolk sac is completely resorbed and the number of myomeres remains the same; seven rays become visible in the caudal fin. The fully formed larva of C. czerskii has an elongated body, a small head, a rounded snout, and an oblong tail part. The melanophores are located in the peritoneal area above the gut, in the abdominal area, and in the postanal ventral row. Armament in the form of spines on the top of the head is absent, pointing to the affiliation of the species that we studied to the Cottus–Leptocottus phenetic group.     

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)     

Spawning habitat and early development of Luciogobius ryukyuensis (Gobiidae)

Egg masses of Luciogobius ryukyuensis were found in spawning grounds around the lowest reach of the adult??s habitat in the tidally influenced area of streams on Okinawa Island. The eggs were attached to the underside of stones and were cared for by a solitary male fish. The number of eggs within an egg mass was 191?C1368. The eggs were elliptical, measuring 2.0?C2.6?mm in length, and 0.6?C0.8?mm in width. Early development of L. ryukyuensis was described from laboratory-reared specimens. Newly hatched larvae, measuring 2.8?C3.3?mm in body length, had an open mouth, pigmented eyes, pectoral fin buds, an orange-colored yolk sac, and characteristic melanophores along the dorsal and ventral midlines of the body. The yolk was completely absorbed at days 2?C3. Notochord flexion began at day 10 and was completed at day 15. The fish started settling on the bottom of the tank at day 34 (14.1?mm in body length) when the body surface started to be covered by intense pigmentation. The eggs and newly hatched larvae of L. ryukyuensis were of standard size of the genus and their morphologies closely resemble those of L. guttatus.     

Direct Effects of Microalgae and Protists on Herring (Clupea harengus) Yolk Sac Larvae

This study investigated effects of microalgae (Rhodomonas baltica) and heterotrophic protists (Oxyrrhis marina) on the daily growth, activity, condition and feeding success of Atlantic herring (Clupea harengus) larvae from hatch, through the end of the endogenous (yolk sac) period. Yolk sac larvae were reared in the presence and absence of microplankton and, each day, groups of larvae were provided access to copepods. Larvae reared with microalgae and protists exhibited precocious (2 days earlier) and ≥ 60% increased feeding incidence on copepods compared to larvae reared in only seawater (SW). In the absence and presence of microalgae and protists, life span and growth trajectories of yolk sac larvae were similar and digestive enzyme activity (trypsin) and nutritional condition (RNA-DNA ratio) markedly declined in all larvae directly after yolk sac depletion. Thus, microplankton promoted early feeding but was not sufficient to alter life span and growth during the yolk sac phase. Given the importance of early feeding, field programs should place greater emphasis on the protozooplankton-ichthyoplankton link to better understand match-mismatch dynamics and bottom-up drivers of year class success in marine fish.     

Riverine life history of the amphidromous goby Sicyopterus japonicus (Gobiidae: Sicydiinae) in the Ota River, Wakayama, Japan

To understand the riverine life history of the amphidromous goby, Sicyopterus japonicus, studies were conducted in the Ota River, Wakayama, Japan. They were distributed from 3 to 23 km upstream from the river mouth, and abundance was higher in the middle reaches than in the upper and lower reaches. Fish were not observed in rapids during winter, suggesting a seasonal change of habitat. Body length ranged from 24 to 120 mm SL. Both females and males ranged from 1 to 6 years old, and males had larger asymptotic length than females. Condition factor showed two peaks in July and November, which appeared to correspond to the spawning season and preparation for over wintering. Gonad somatic index increased in summer with a peak in August indicating a summertime spawning season that was confirmed by collections of the newly hatched larvae migrating downstream. Eggs of 0.5 mm diameter were attached to stones and newly hatched larvae made continuous vertical movements of sinking and upward swimming and the distance of each movement was longer in freshwater than in seawater. The newly hatched larvae were collected at nighttime (19:00–24:00) mainly in August. Those larvae were very small (mean: 1.4 mm TL) with a yolk sac and no eye pigmentation. Low wintertime temperatures are likely an important determinant of the spawning and recruitment seasons and seasonal changes of activity of this species that lives at much higher latitudes than all other species of the subfamily.     

The Spawning and Early Life History of the Pollan (Coregonus pollan THOMPSON) in Lough Neagh,Northern Ireland

Studies had been carried out on the local non-migratory whitefish. Spawning behaviour and light conditions on the spawning ground are recorded. After artificial spawning, embryonal development took place under controlled conditions and the larvae were reared. Detailed characteristics of swim bladder creation and differentiation of the digestive tract are given. Distribution and number of pollan larvae near the spawning area and in the open lake were examined. Data are presented concerning the growth rates of larvae and fry in captivity and under lake conditions. Ecological data related to other coregonids are discussed and compared with the present study.     

Post‐hatch dispersal of lake sturgeon (Acipenser fulvescens,Rafinesque, 1817) yolk‐sac larvae in relation to substrate in an artificial stream

Knowledge of the effects of environment and genotype on behavior during early ontogenetic stages of many fish species including lake sturgeon (Acipenser fulvescens) is generally lacking. Understanding these effects is particularly important at a time when human activities are fundamentally altering habitats and seasonal and diel physical and biotic stream features. Artificial stream channels were used in a controlled experiment to quantify lake sturgeon yolk‐sac larvae dispersal distance and stream substrate preference from different females (N = 2) whose eggs were incubated at different temperatures (10 and 18°C) that simulated stream conditions during early and late spawning and incubation periods in the Black River, Michigan. Data revealed that yolk‐sac larvae exhibited considerable variability in dispersal distance as a function of family (genotype), temperature experienced during previous (embryonic) ontogenetic stages, and environmental ‘grain’. Yolk‐sac larvae dispersal distance varied as a function of the juxtaposition of substrate to location of egg hatch. Lake sturgeon yolk‐sac larvae dispersed from mesh screens attached to bricks and settled exclusively in gravel substrate. Dispersal distance also varied as a function of family and egg incubation temperatures, reflecting differences in offspring body size and levels of endogenous yolk reserves (yolk sac area) at hatch. Expression of plasticity in dispersal behavior may be particularly important to individual survival and population levels of recruitment contingent upon the location, size, and degree of fragmentation of suitable (gravel) habitats between adult spawning and yolk‐sac larvae rearing areas.