Osteological development of the lophiid anglerfish,lophius gastrophysus

The osteological development of the head skeleton and dorsal, pectoral, and anal fin supports, are described from cleared and stained specimens ofLophius gastrophysus larvae, ranging from 4.6 to 21.8 mm NL; the results are compared with those of juvenile (79.8 mm SL) and adult (398 mm SL) specimens. Tiny conical teeth are present on the premaxillary, dentary, palatine and vomer since early stage. The first three dorsal fin spines are initially positioned on the midline of body posterior to the supraoccipital, but they migrate forward with growth and become cephalic in juveniles. The forward movement of the dorsal spines is produced by the forward extension of the cartilaginous basal inside the subepidermal space. During the planktonic larval stage the pectoral fins are on the sides of body as in ordinary fishes, but they move ventrad and become leg-like in bottom living juveniles and adults. Ossification of the caudal complex ofL. gastrophysus larvae proceeds very slowly and only the 21.8 mm NL larva has an almost completely ossified caudal complex. Eight principal caudal rays are loosely attached on the posterior edge of the hypurals and no procurrent rays are present. Larvae have well developed parhypurapophysis at the mid-portion of the urostyle which transforms into keel-like structure in juveniles and adults.     

Description of transformation larvae and a juvenile of the dextral flounder,poecilopsetta praelonga (pleuronectidae, poecilopsettinae) from the northwestern waters of australia

Three late metamorphic transformation larvae ofPoecilopsetta praelonga (68.0–82.3 mm SL) and a juvenile (92.7 mm SL) captured from the waters off northwestern Australia (400–460 m deep) are described. The transformation larvae ofP. praelonga are distinguishable from the congeners of the same stage in having relatively low body depth (2.20–2.44 in SL), relatively large maxilla extending to anterior one-third of lower eye, and seven and six distinct spots along the dorsal and ventral margins of ocular side body, respectively. In the smallest specimen, the intestine was expanded posteriorly beyond the posterior wall of visceral cavity, but not in the larger specimens. The pectoral fin rays and the spines of scales were supposed to begin to be formed by about 80 mm SL. Ontogenetic changes which include decreasing ratios of upper jaw length to head length. and increasing ratios of depth of body muscle to body depth, were observed, based on a comparison of transformation larvae, a juvenile and adults.     

Morphological development of larval and juvenile Alectis indica (Perciformes: Carangidae) reared in captivity

Larvae and juveniles of Alectis indica reared in captivity are described based on 47 specimens (3.2–32.0 mm in body length: BL). Development was typical for the tribe Carangini except for the presence of elongated fin filaments. Elongated dorsal-fin filaments were present at preflexion (3.2 mm BL). During flexion, the anal- and pelvic-fin rays elongated and the body deepened. The full complement of fin spines and rays was present by 7.1 mm BL. The larvae of A. indica could be differentiated from those of Alectis ciliaris, which also inhabits in the Indo-Pacific waters, by the presence of a ventral series of melanophores on the tail, elongated pelvic fins, and the timing of anal-fin spine migration. The rounded body and elongated fin rays of A. indica cause it to resemble venomous Cubomedusae.     

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.     

Promyllantor atlanticus (Anguilliformes, Conridae), a new species from the continental slope of southwestern Africa

Promyllantor atlanticus sp. nova is described from two specimens (the holotype TL 518 mm) from waters of southeastern Atlantic west of Congo (6°14′S, 11°24′E) at the depth of 495 m. It differs from a similar species in the number of vertebrae species P. adenensis in longer pectoral fins, deeper head, and fewer pores in the suborbital and mandibular canals.     

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.     

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.     

Occurrence of Larval and Juvenile Japanese Snook, <Emphasis Type="Italic">Lates japonicus</Emphasis>, in the Shimanto Estuary,Japan

A total of 54 postlarval, 12 juvenile and six young Lates japonicus were collected in the Shimanto estuary from August 1985 to January 1987. The larvae (4.3–7.6 mm SL) and juveniles (8.1–28.0 mm SL) occurred only in areas with eelgrass beds from late July to middle August. Temperatures and salinities at waters where any number of them were collected ranged from 27.8 to 31.9°C and from 2.8 to 18.2%, respectively. The larvae are very similar in general morphology to those of Mugilidae and some of Gobiidae, but are distinguished from others by the spines of preopercle, position of the anus and pigmentation patterns in the posterior part of body.     

Larval developmental stages of laboratory-reared silver pomfret,pampus argenteus

Eggs of the silver pomfret,Pampus argenteus, were collected and artificially fertilized by stripping fully-ripe male and female broodstock caught by gillnets in Kuwait waters during June 1997. Larvae hatched from fertilized eggs were reared until 90 days after hatching (DAH) in water temperatures of 27–30°C. Newly-hatched larvae grew from an average of 2.4 mm in body length (BL) to 3.7, 4.4, 7.2 and 8.4 mm at 8, 12, 24 and 30 DAH, respectively. Myomere and vertebral numbers ranged from 34 to 36. Transformation from the larval to juvenile form was completed at 22.2 mm BL (40 DAH). Dorsal and anal fin spines first appeared when juveniles reached 38.8 mm BL (50 DAH). Body depth increased with increase in body length; a rapid increase in body depth occurred in larvae 7.1–8.0 mm, reaching 57% of BL, and further increased to 69% of BL in juveniles 38.8 to 47.9 mm. Pigmentation during development is described and illustrated.     

Growth and morphological development of laboratory-reared larval and juvenile snakeskin gourami Trichogaster pectoralis

Morphological development, including that of fins, labyrinth organ, body proportions, and pigmentation, in laboratory-hatched larval and juvenile snakeskin gourami Trichogaster pectoralis is described. Body lengths (BL; mean ± SD) of larvae and juveniles were 2.3 ± 0.1 mm just after hatching (day 0) and 8.2 ± 0.6 mm on day 22, reaching 14.1 ± 2.3 mm on day 48. Aggregate fin ray numbers attained their full complements in juveniles >11.8 mm BL. Preflexion larvae started feeding on day 2 following upper and lower jaw formation, the yolk being completely absorbed by day 12. Subsequently, oblong conical teeth appeared in postflexion larvae >8.2 mm BL (day 16). Melanophores on the body increased with growth, with a large dark spot developing on the lateral midline at the caudal margin of the body in flexion larvae >6.1 mm BL. Subsequently, a broad vertical dark band from the eye to the caudal peduncle developed in postflexion larvae >8.9 mm BL. Proportions of head and pre-anal lengths became constant in postflexion larvae greater than ca. 9–10 mm BL, whereas those of maximum body depth, eye diameter, and snout length failed to stabilize in fish of the size examined in this study. First soft fin ray of the pelvic fin elongated, reaching over 40% BL. The labyrinth organ differentiated in postflexion larvae >7.4 mm BL (day 22). Comparisons of larval and juvenile morphology with another anabantoid species Anabas testudineus were also made, revealing several distinct differences, particularly in the numbers of myomeres and fin rays in the dorsal/anal fins, mouth location and body shape.     

Chromis okamurai,a new damselfish from the Okinawa Trough,Japan

A new pomacentrid fish,Chromis okamurai, is described from a single specimen taken from the Okinawa Trough (25°53.4′N, 123°59.4′E), in 135–175 m. This species is most closely related to the deep-dwellingC. mirationis, sharing with it the same meristic data (in particular XIV dorsal spines and 2 upper and lower caudal spinules), large eye, and relatively deep body. It differs in having a small round posterior nostril (large and slit like inmirationis), longer second anal spine, shorter pelvic fins, and in color: two dark brown stripes on body and a pale pectoral-fin axil (mirationis has a single, midlateral, yellow to yellowish brown stripe which extends broadly onto lower part of caudal fin, and a black pectoral axil).     

Description of juvenile development ofArtediellus neyelovi (cottidae) from off Usujiri, southern Hokkaido, Japan

Juveniles ofArtediellus neyelovi are described on the basis of 24 specimens (8.3–23.6 mm SL) from Hokkaido, Japan. All medial and paired fins were completely developed in all specimens. The smallest specimen (8.3 mm SL) had a slender elongated suborbital stay similar to that of adults. Specimens 8.3–10.1 mm SL had 4 preopercular spines, cirri absent on the head and body, except a very small supraorbital cirrus, and sensory canals comprising open grooves restricted to the head surface. Specimens 14.1–20.0 mm SL had complete cephalic sensory canals, and the 2nd and 3rd preopercular spines reduced. Specimens 20.8–23.6 mm SL had a nearly complete lateral line canal and exhibited most specific diagnostic characters except some cephalic cirri. The anterior 3 neural arches on both sides were separate at 8.3 mm SL, but had become fused (except for the anteriormost) at 14.3 mm SL. The anteriormost arch was not fused in an adult, 71.3 mm SL. Some juveniles had very reduced bony plates under the skin anterodorsally on the body, which were not present in adults.     

Larvae and juveniles of blue drum,Nibea mitsukurii,occurring in the surf zone of Tosa Bay,Japan

A total of 211 larval and juvenileNibea mitsukurii (4.0–19.0 mm SL) was collected with a small seine in surf zones of Tosa Bay during the period of May 1981 to June 1984. They had morphological characteristics common to the larvae and juveniles of Sciaenidae, but were distinguished from the others by the distribution pattern of melanophores on body and spines at the anterior tip of maxillary. They occurred only in surf zone of Tei out of three locations facing Tosa Bay from middle May to middle August. Temperatures and salinities at the place when they were collected ranged from 21.7 to 29.5°C and from 24.5 to 31.3‰, respectively. Good catches were observed when minute dusts floated abundantly in the surf zone. In past studies using traditional larval nets or minnow-nets in coastal or shallow waters of Tosa Bay, larval and juvenileN. mitsukurii were not reported. It seems that they occur in association with minute dusts in extremely shallow waters such as surf zones.     

Morphological aspects of the development of swimming and feeding functions in the milkfishChanos chanos

Development of swimming and feeding abilities based on morphological development of larval and early juvenileChanos chanos was investigated. In larvae smaller than about 6.5 mm SL, mechanical supports of fins and branchial arches were in a primordial stage of development. Supports and rays of the vertical fins and branchial arches rapidly developed from 6.5 mm SL, and all components appeared by about 10.5 mm SL. Thereafter body depth proportion changed and the supports and rays of the paired fins and gill-rakers developed. These developmental events were nearly or totally completed by about 17 mm SL, and we concluded that the larvae transformed to juveniles at this size. By this time, the mode of swimming of the fish shifted from undulating locomotion to caudal propulsion and that of feeding from swallowing paniculate food to filtering and concentrating substrate food matters using gill-rakers and the epibranchial organ. One of the most characteristic, and well-known, phenomena in the life history ofChanos chanos is the mass occurrence in the surf zone of postlarvae of a limited size range. In view of the scheme of the development of mechanical supports of the body and fins, they may acquire a swimming ability strong enough to move against the current only upon reaching about 10.5 mm SL, and if active shoreward migration of the larvae occurs, it is only during the late period of their journey from the spawning grounds to the shore. The sudden disappearance from the surf zone of larvae larger than 15–16 mm SL is obviously related to a change in food habit.     

Growth and morphological development of larval and juvenileepinephelus bruneus (perciformes: Serranidae)

The growth and morphological development of larval and juvenileEpinephelus bruneus were examined in a hatchery-reared series. Average body length (BL) of newly-hatched larvae was 1.99 mm, the larvae growing to an average of 3.96 mm by day 10, 6.97 mm by day 20, 12.8 mm by day 30, 22.1 mm by day 40 and 24.7 mm by day 45 after hatching. Newly-hatched larvae had many mucous cells in the entire body epidermis. By about 4 mm BL, the larvae had developed pigment patterns peculiar to epinepheline fishes, including melanophores on the dorsal part of the gut, on the tips of the second dorsal and pelvic fin spines, and in a cluster on the ventral surface of the tail. Spinelets on the second dorsal and pelvic fin spines, the preopercular angle spine and the supraocular spine, had started to develop by about 6 mm BL. The notochord tip was in the process of flexion in larvae of 6–8 mm BL, by which time major spines, pigments and jaw teeth had started to appear. Fin ray counts had attained the adult complement at 10 mm BL. After larvae reached 17 mm BL, elements of juvenile coloration in the form of more or less densely-pigmented patches started to appear on the body. Squamation started at 20 mm BL. Major head spines had disappeared or became relatively smaller and lost their serrations by 20–25 mm BL.     

Metarhizium spp. isolates from madagascar: Morphology and effect of high temperature on growth and infectivity to the migratory locust,Locusta migratoria

Five strains ofMetarhizium anisopliae (Metsch.) Sorokin and one strain ofMetarhizium flavoviride Gams &; Rozsypal originally isolated in Madagascar were studied. Measurements of conidia and, for the first time, also of blastospores produced in a liquid medium were used for species and variety determination. Blastospores ofM. flavoviride were more homogenous in their size than those ofM. anisopliae. Growth at high temperatures between 25° and 40°C showed that 4 isolates ofM. anisopliae grew at 36°C andM. flavoviride grew at 38°C. Using alternating day/night temperatures (8/16 h) the three strains tested could also tolerate 40°/25°C. In bioassays, fiveMetarhizium spp. isolates were tested against third and fourth instar larvae ofLocusta migratoria (L.) at two alternating day/night temperatures of 30°/25°C and 36°/25°C. In the cooler regime, all strains caused a mortality of 50% within 5.9 to 8.5 days (median lethal time), while in the 36°/25°C treatment only the thermophilicM. flavoviride and oneM. anisopliae strain isolated from a soil sample gave comparable results with median lethal times of 6.8 and 7.3 days, respectively.     

Larval development of the Indo-Pacific perciform fish,Centrogenys vaigiensis (Pisces: Centrogeniidae)

Based on seven larvae from northern Australia, development ofCentrogenys vaigiensis—a species of uncertain phylogenetic affinities—is described for the first time. Identification was established from meristic and osteological characters. Development is characterized by few morphological specializations and is apparently completed at a small size (ca 5 mm standard length). Larvae are deep-bodied and compressed, with very limited head spination (small spines on preopercle, subopercle, opercle and supracleithrum). Fin development takes place at about the time of notochord flexion, and is complete at about 4.3 mm, with the exception of anal spine three, which does not fully transform from a soft ray until after settlement. Fin spines are short, smooth and weak. Larvae are apparently limited to near-shore, shallow marine waters, and based on the size of what are apparently settlement-stage larvae, the pelagic period may be short.     

Early ontogeny of the big roughy Gephyroberyx japonicus (Beryciformes: Trachichthyidae) in captivity

Development of eggs and larvae of the big roughy Gephyroberyx japonicus are described on the basis of specimens reared in captivity. Spherical eggs (diameter 1.26–1.35?mm) with a single oil globule were pelagic. Newly hatched larvae (2.8–3.1?mm in body length, BL) had strong linear pigmentation on the head and trunk. The mouth opened at ca. 3.5?mm BL; thereafter the yolk was absorbed. Notochord flexion started at ca. 4.5?mm BL when body depth increased rapidly, and melanophores spread to all of the body. Notochord flexion was completed at ca. 5.0?mm BL. Head spination and pelvic fins began to develop during the flexion stage.     

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.     

External Morphology of Lophiosilurus alexandri Steindachner, 1876 during Early Stages of Development,and Its Implications for the Evolution of Pseudopimelodidae (Siluriformes)

Pseudopimelodidae are Neotropical catfishes characterized by having slightly to strongly depressed body in fully developed specimens. The largest species of the family with 500 mm SL, Lophiosilurus alexandri, experiences impressive changes in body shape during development, becoming extremely depressed when fully developed. Accordingly, Lophiosilurus alexandri is an ideal species to observe the morphological changes during ontogeny, and to seek solid interpretations on the polarity of characters. Specimens of distinct larval periods (yolk sac, flexion and postflexion; n = 186 specimens) and juvenile stages (n = 20) were analyzed. Changes in body shape, position of mouth and eye, morphology of fins and pigmentation were observed during the development of Lophiosilurus. Larvae (5.7–11.2 mm standard length) had pigmentation concentrated on the head and parts of body, eyes small and pigmented, short barbels, and well-developed finfold. Juveniles (15.9–28.1 mm standard length) had body shape similar to adult, with head depressed and bearing bony ridges, large mouth, dorsally-oriented eyes, small barbels and well-developed shoulder bulges (cleithral width). The greatest morphological changes in the development of L. alexandri occurred during the postflexion larval stage. Relative to standard length, measurements of snout length, head depth and body depth are smaller in juveniles than in larvae, but body width is larger. New interpretations on the phylogenetic characters related to these changes are provided in view of the two alternative hypotheses of the evolution of Pseudopimelodidae.