Larvae and juveniles of the plunderfishes <Emphasis Type="Italic">Artedidraco shackletoni</Emphasis> and <Emphasis Type="Italic">A.</Emphasis><Emphasis Type="Italic">skottsbergi</Emphasis> (Notothenioidei,Artedidraconidae) from the Indian sector of the Southern Ocean

Early life stages of Artedidraco skottsbergi and A. shackletoni were collected off Adélie Land. The morphology and pigmentation pattern of nine larvae and juveniles of A. skottsbergi between 17.2 and 21.4 mm in standard length (SL), and of two juveniles of A. shackletoni measuring 25.1 mm SL were described. A. skottsbergi was characterized by a heavily pigmented body, except for the caudal peduncle, with distinctively dense pigmentation on the ventrolateral half of the body and caudal section (17.2–17.9 mm SL). Furthermore, they had no pigmentation on the pectoral fin base until they attained 21.4 mm SL. Juvenile A. shackletoni had a heavily pigmented body except for the ventral side of the abdomen and the anal fin base. The proximal part of the dorsal fin and most of the anal fin were covered with melanophores. Although knowledge of larval and juvenile Artedidraco species is limited, the distribution of melanophores on the fins, pectoral fin base and caudal peduncle at each developmental stage may be useful for species identification.     

The maturity and breeding season of the bellybarred pipefish, <Emphasis Type="Italic">Hippichthys spicifer</Emphasis>, in Okinawa-jima Island rivers

We investigated the breeding season and size at maturation and described the morphology of newly released Hippichthys spicifer larvae collected from the estuaries of four rivers on northern Okinawa-jima Island, southern Japan. The minimum size of brooding males was 108 mm standard length (SL). The smallest mature female, as estimated from gonadosomatic index (GSI) analysis and histological observations of gonads, was about 100 mm SL. Histological observations showed the gonad of H. spicifer to be a cylindrical tube with a sequential pattern of follicle development and a single germinal ridge. We surmised that the breeding season is year-round, as shown by monthly changes in female GSI, gonad histology, and monthly changes in the occurrence of brooding males. The monthly changes in female GSI and proportions of brooding males were small in winter. The number of eggs in the male brood pouch ranged from 114 to 1,764 (604.4 ± 322.8, mean ± standard deviation; n = 25). The SL of the released larvae was 9.9 mm. All fins except the pectoral fins were formed, the body was elongated, and the developmental stage was similar to that of other Urophori species. The smallest individual present in the mangrove areas of estuaries was 78.0 mm SL.     

Embryonic development of the threatened freshwater pipefish Microphis deocata (Hamilton, 1822)

The present study provides the first comprehensive embryonic development of the freshwater Syngnathid fish species, Microphis deocata (Hamilton), a Near Threatened pipefish endemic to the Brahmaputra River drainage in Northeast India and Bangladesh. Microphis deocata is a Gastrophori species as the males develop an abdominal brood pouch. Mature individuals were collected and maintained in well-aerated aquaria under controlled conditions to induce natural spawning. The number of eggs within the males' brood pouch ranged from 17 to 22 (for n = 10), measuring 0.7–1.0 mm in diameter. A total of 10 developmental stages could be recognized under four developmental periods namely, early embryogenesis, eye development, snout formation and juvenile. However, sensitivity, and therefore mortality, while handling of this species restricted the study from reporting the exact time intervals for stages following the blastodisc formation ~48 hr post fertilization. A newborn larvae measures ~14 mm and is free-swimming with distinct dorsal fin (with 31–32 rays) and a sector-shaped caudal fin (with 8–9 rays). The study aims to provide baseline information on the embryology of M. deocata in culture condition which will be helpful for future studies on conservation biology, population status and management of this species.     

Notes on the morphology of the early stage of the rare bramid genus Eumegistus

The morphology of the early stage of Eumegistus was described from three specimens [E. brevorti: 23.0 mm in standard length (SL) juvenile; E. illustris: 5.8 mm SL postflexion larva, and 40.0 mm SL juvenile] recently rediscovered in museum collections. Larval and juvenile pigmentation patterns were reported for the first time for this genus. The 5.8 mm SL postflexion larva of E. illustris had pigmentation on the head and anterior half of the body, through to the middle of the dorsal fin base. In larvae and juveniles of both species, the outer side of the pelvic fin was pigmented. The two juveniles possessed several spines on the lachrymal and protruding rays in the middle of the caudal fin. Although it is known previously that the notochord flexion occurs at 5.0–6.0 mm SL in E. brevorti, the reexamined 5.0 mm SL specimen had the notochord completely flexed. Furthermore, we could not confirm whether the previously studied 4.0 mm SL specimen was E. brevorti because it was badly damaged.     

Growth and morphological development of laboratory-reared larval and juvenile climbing perch <Emphasis Type="Italic">Anabas testudineus</Emphasis>

Morphological development, including fin and labyrinth organ, body proportions and pigmentation, in laboratory-reared larval and juvenile climbing perch Anabas testudineus was described and behavioral features under rearing condition were observed. Body lengths (BL) of larvae and juveniles were 1.9 ± 0.1 (mean ± SD) mm just after hatching (day-0), 8.7 ± 1.3 mm on day-19, reaching 18.4 ± 2.1 mm on day-35 after hatching. Aggregate fin ray numbers attained full complements in juveniles larger than 8.3 mm BL. Preflexion larvae started feeding on day-2 following formation of the upper and lower jaws, the yolk being completely absorbed by day-7 after hatching. Teeth appeared in flexion larvae larger than 5 mm BL on day-6, with cannibalism starting shortly after and continuing with further growth. Melanophores on the body increased with growth, a large dark spot developing on the lateral midline around caudal margin of the body in the postflexion and juvenile stages. The labyrinth organ differentiated in postflexion larvae larger than 7.2 mm BL on day-16, with air-breathing starting at the same time. Body proportions attained constant in postflexion larvae larger than 7.0 mm BL, and habitat of fish shifted from bottom to mid-layer. With the exception of fin ray numbers, the above morphological developments corresponded to behavioral shifts that occurred in the postflexion stage (ca. 7 mm BL), their subsequent continuity illustrating that the species possessed most juvenile-equivalent functions from ca. 7 mm BL.     

Recruitment of amphidromous sleepers Eleotris acanthopoma, Eleotris melanosoma, and Eleotris fusca into the Teima River, Okinawa Island

Recruitment courses of three amphidromous sleeper species, Eleotris acanthopoma, E. melanosoma, and E. fusca, were investigated at the surf zone adjacent to the river mouth and at five stations in the Teima River on Okinawa Island, Japan. All three species occurred at the surf zone as pelagic larvae with transparent and compressed body, a conspicuous air bladder, and an emarginated caudal fin. Eleotris fusca (16.0–19.6 mm in standard length: SL) sometimes possessed a vestige of the larval chin barbel and were larger than E. acanthopoma (9.7–13.2 mm SL) and E. melanosoma (11.2–12.8 mm SL). The pelagic larvae were also collected during full tide from the lower reaches of the tidally influenced area of the river. The pelagic larvae may be carried in and out of the estuary with some tidal fluxes, and they may settle when they reach the upper tidally influenced area where the salinity becomes extremely low. Body width and pigmentation of newly settled larvae increased. E. fusca was considered to migrate upstream to the freshwater area against the flow of the river just after reaching the settled stage. After settlement, all three species became completely pigmented, the caudal fin became round in shape, and the fin ray counts became complete with growth. Also, E. acanthopoma dispersed widely to the lower part of the tidally influenced area or to the lower reaches of the freshwater area, E. melanosoma dispersed to the lower part of the tidally influenced area, and E. fusca dispersed upstream.     

Larval and juvenile Polymetme elongata (Stomiiformes: Phosichthyidae) collected from Suruga Bay and offshore waters, Japan

Two larvae [17.4 mm standard length: SL (postflexion stage)] and 26.1 mm SL (transformation stage)] and a juvenile (31.7 mm SL) of a phosichthyid, Polymetme elongata, from Suruga Bay and offshore waters, central Japan, are described. These specimens had an elongate body with relatively short preanal length (53–63% SL), long anal fin base (2.6–3.4 times dorsal fin base length), and anal fin origin below dorsal fin base, and were further characterized by a blackish flap on each eye and internal clusters of melanophores (e.g., along caudal myosepta around midlateral line and on ventral margin of caudal peduncle). The short preanal length and larval melanophore pattern were very similar to those of another phosichthyid, Yarrella blackfordi, from the Atlantic Ocean.     

Juvenile development of a flathead,Suggrundus meerdervoortii (Scorpaeniformes: Platycephalidae)

Juvenile development ofSuggrundus meerdervoortii was described, based on twelve specimens (12.9–43.8 mm SL) collected from off Yamagata Prefecture, Japan Sea. Two exterior openings in the lateral line scales were completed at ca. 35 mm SL, with the interopercular flap and iris lappet being visible at ca. 44 mm SL, these all being useful taxonomic characters. In juveniles and additional young and adult specimens (ca. 70–191 mm SL), the proportions of head length, snout length, orbital diameter, caudal peduncle depth and caudal fin length decreased with growth; interorbital width decreased rapidly until ca. 70 mm SL, but more or less stabilised thereafter (70–191 mm SL).     

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.     

Juveniles of two sillaginids,Sillago aeolus andS. sihama,occurring in a surf zone in the Philippines

Sillaginid juveniles collected from the surf zone at Tigbauan, Iloilo, Philippines, between May 1986 and September 1987 were identified asSillago aeolus (n=702, 8.9–26.0 mm SL) andS. sihama (n=3414, 8.6–22.9 mm SL), based on the numbers of dorsal and anal soft fin rays and vertebrae. The two species were easily distinguishable by the pattern of melanophores distributed on the caudal fin base,S. aeolus having a triangular-shaped cluster, whereas the melanophores formed a vertical line inS. sihama. The ratios of pre-anal and caudal peduncle lengths to SL also differed between the species, both being higher inS. aeolus. The occurrence ofS. aeolus was limited to the dry season, from January to March. On the other hand,S. sihama occurred year-round, although a peak was observed in the dry season, from November to April.     

Growth and morphological development of laboratory-reared larval and juvenile three-spot gourami <Emphasis Type="Italic">Trichogaster trichopterus</Emphasis>

Morphological development, including the body proportions, fins, pigmentation and labyrinth organ, in laboratory-hatched larval and juvenile three-spot gourami Trichogaster trichopterus was described. In addition, some wild larval and juvenile specimens were observed for comparison. Body lengths of larvae and juveniles were 2.5 ± 0.1 mm just after hatching (day 0) and 9.2 ± 1.4 mm on day 22, reaching 20.4 ± 5.0 mm on day 40. Aggregate fin ray numbers attained their full complements in juveniles >11.9 mm BL. Preflexion larvae started feeding on day 3 following upper and lower jaw formation, the yolk being completely absorbed by day 11. Subsequently, oblong conical teeth appeared in postflexion larvae >6.4 mm BL (day 13). Melanophores on the body increased with growth, and a large spot started forming at the caudal margin of the body in flexion postlarvae >6.7 mm BL, followed by a second large spot positioned posteriorly on the midline in postflexion larvae >8.6 mm BL. The labyrinth organ differentiated in postflexion larvae >7.9 mm BL (day 19). For eye diameter and the first soft fin ray of pelvic fin length, the proportions in laboratory-reared specimens were smaller than those in wild specimens in 18.5–24.5 mm BL. The pigmentation pattern of laboratory-reared fish did not distinctively differ from that in the wild ones. Comparisons with larval and juvenile morphology of a congener T. pectoralis revealed several distinct differences, particularly in the numbers of myomeres, pigmentations and the proportional length of the first soft fin ray of the pelvic fin.     

Pelagic larvae of Ventrifossa garmani (Gadiformes: Macrouridae) from Suruga Bay and offshore waters of Japan

Three pelagic larvae [5.1–5.9 mm in head length (80+ to 101+ mm in total length)] of a macrourid fish, Ventrifossa garmani, from Suruga Bay and offshore waters of central Japan are described. The specimens were characterized by a remarkably elongate caudal region (caudal region length >15.6 times head length), the longest known to date among macrourid larvae and juveniles. Other characteristics included a short snout, first dorsal and pelvic fin rays not elongated, external melanophores on most of the body and posteriorly on the anal fin membrane, and six or seven rectangular clusters of internal melanophores laterally on the anterior caudal region.     

A description of the smallest Triodon on record (Teleostei: Tetraodontiformes: Triodontidae)

The smallest known specimen (20mm standard length: SL) of Triodon macropterus Lesson is described and illustrated. It is easily distinguished from superficially similar tetraodontid and diodontid larvae or early juveniles of comparable size by the following characters: separate premaxillae in conjunction with the fused dentaries; the presence of multicuspid spinoid scales; the jet-black mark in front of the soft dorsal fin; the developing pelvis, which is visible through the distended skin of the belly; and the presence of a number of procurrent caudal fin rays. The small Triodon differs from the adult in possessing a huge head that measures 45% SL (vs. 28.5–32.7% in adult), the absence of the characteristic dewlap with the conspicuous lateral ocellus, and the structure of the scales and nostrils.     

Juveniles of Kyphosus vaigiensis (Quoy and Gaimard 1825) with reference to a senior synonym of Cantharus lineolatus Valenciennes 1830

The juveniles of Kyphosus vaigiensis (Quoy and Gaimard 1825), collected from the Indian Ocean and Japanese waters, are described with some ontogenetic morphological changes based on six specimens having 14 dorsal and 13 anal fin soft rays, 56–62 scales in a longitudinal row along the midbody, and 30–32 gill-rakers on the first gill-arch. The juveniles of K. vaigiensis smaller than ca. 42 mm in standard length (SL) have the proximal parts of the dorsal and anal fin soft-rayed portions covered with small scales, and the single outer row of the upper jaw teeth consisting of incisor-like and conically pointed teeth, the former with polycuspid tips differing from the specimens greater than ca. 68 mm SL. The holotype of Cantharus lineolatus Valenciennes 1830, 41.5 mm SL, was included here in the juveniles as K. vaigiensis. Therefore, K. vaigiensis is recognized as a senior synonym of C. lineolatus.     

Juvenile morphology and occurrence patterns of three Butis species (Gobioidei: Eleotridae) in a mangrove estuary, southern Thailand

Juveniles of three eleotrid Butis species (B. butis, B. humeralis, and B. koilomatodon) are described; their occurrence patterns were examined in Sikao Creek, a mangrove estuary located in southern Thailand. Juveniles of each species were distinguished by the following characters: B. butis with no bands on body and pale pelvic fins; B. humeralis with no bands on body and densely pigmented pelvic fins; and B. koilomatodon with 5–6 regular bands on body and a fleshy process (preorbital knob) on the snout. Although B. butis shared the aforementioned characters with B. amboinensis found in the same estuary, the former was distinguished from the latter by having a greater number of pectoral fin rays (18–21 vs. 17) and a deeper caudal peduncle. Distribution patterns of the three Butis species in Sikao Creek were distinguishable from each other. Smaller B. butis [mean ± SD = 22.7 ± 16.9 mm in standard length (SL), n = 32] occurred in the upper reach of the estuary, while larger specimens (52.4 ± 26.2 mm SL, n = 18 and 51.5 ± 29.7 mm SL, n = 10, respectively) were found in the middle and lower reaches and none in the marine area. In B. humeralis and B. koilomatodon, only juveniles were caught except for one adult specimen each. Juveniles (8.9–16.5 mm SL, n = 79) of B. humeralis occurred in the upper and middle reaches and the marine area. B. koilomatodon juveniles (9.9–13.7 mm SL, n = 30) were distributed in all areas from the lower to upper reaches.     

Development of eggs, larvae and juveniles of laboratory-reared blue whiting,Sillago parvisquamis (Percoidei: Sillaginidae)

The embryonic, larval and juvenile development of blue whiting,Sillago parvisquamis Gill, are described from a series of laboratory-reared specimens. Mean egg diameter and mean total length (TL) of newly-hatched larvae were 0.71 mm and 1.58 mm, respectively. The eggs were non-adhesive, buoyant and spherical with an oil globule (mean diameter 0.18 mm). Hatching occurred about 20 hours after fertilization at a temperature of 24.0–25.0°C, newly-hatched larvae having 38–40 myomeres. The yolk and oil globule were completely absorbed 3 days after hatching at 2.8–3.2 (mean 3.0) mm TL. Notochord flexion was completed by 7.2–8.2 (7.7) mm TL, and pectoral and caudal fin rays fully developed by approximately 10 mm and 8.5 mm TL, respectively. Completion of fin development occurred in the following sequence: caudal, pectoral, anal and second dorsal, first dorsal and pelvic, the last-mentioned by approximately 11 mm TL. The larvae ofS. parvisquamis andS. japonica, which closely resemble each other in general morphology and pigmentation, could be distinguished as follows. Newly-hatchedS. parvisquamis larvae had more myomeres thanS. japonica (38–40 vs. 32–34) and more melanophores on the dorsal surface of the body (19–28 vs. about 40).Sillago japonica had a vertical band of melanophores on the caudal peduncle, which was lacking in postflexionS. parvisquamis larvae. In addition, juveniles ofS. parvisquamis (larger than 23 mm TL) had melanophores on the body extending anteriorly to below the lateral line to form a midlateral band, whereas no obvious band occurred on similarly-sizedS. japonica juveniles.     

Osteological development in the Japanese sardine,Sardinops melanostictus

The development of all osteological elements, except scales, of the Japanese sardine,Sardinops melanostictus, is described from newly-hatched larvae to adult fishes. Newly-hatched larvae lacked osteological elements. Part of the head skeleton began to develop in 53 hour old larvae (4.2 mm in notochord length [NL]). Larvae at the first-feeding stage (77 hours, 5.5 mm NL) possessed several elements of the head skeleton and pectoral fin supports. In a 10.5 mm NL specimen, part of the caudal and dorsal fin supports were apparent. The centra appeared in specimens 18–22.7 mm in standard length (SL). Gill rakers were first observed in the lower branchial arches at 13 mm NL and spine-like processes with spiny nodules from about 25 mm SL. The distance between the predorsal and first dorsal proximal radial relative to SL rapidly decreased with forward translocation of the dorsal fin and became constant beyond approximately 34 mm SL. At this stage, most basic osteological elements were established. Completion of the osteological structure was characterized by the disappearance of the dentary teeth at 60–70 mm SL. Based on the osteological development, ontogenetic intervals consisting of four periods and eight phases were recognized.     

The early life history of kurosoi,Sebastes schlegeli (Scorpaenidae), in the Sea of Japan

Larval and juvenile stages of kurosoi,Sebastes schlegeli, are described and illustrated from wild specimens. Some ecological aspects of larvae and juveniles are also described. Notochord flexion occurred between 5.6–7.5 mm SL. Transformation occurred between 13–20 mm SL. Preflexion and flexion larvae ofS. schlegeli can be distinguished from similar larvae by the pigmentation of the dorsal and ventral midlines of the tail and absence of pigmentation on the ventral portion of the rectum. After notochord flexion, the dorsal and lateral regions in both larvae and pelagic juveniles were heavily pigmented, suggesting adaptation for neustonic life style. Larvae and juveniles were caught at many coastal stations, but did not occur in cooler offshore waters. Larvae smaller than 20 mm SL inhabited surface waters. Until ca. 40 mm SL, juveniles inhabited mainly surface waters (without drifting seaweed), but also used other habitats, such as the drifting seaweed, and near the sea bed. Small larvae (<7 mm SL) fed mainly on copepod nauplii. Larger larvae fed on calanoid copepodites andEvadne nordmanni. Pelagic juveniles fed mainly on fish eggs, with fish larvae also being important food items for some individuals. Most food items taken by juveniles that were associated with drifting seaweed were eggs with attaching filaments (Cololabis saira andHyporhamphus sajori), suggesting that the high density of such food items both attracts and keeps juveniles around drifting seaweed.     

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.     

Use of water hyacinths as shelter,foraging place,and transport by young piranhas,Serrasalmus spilopleura

Synopsis The water hyacinth, Eichhornia crassipes, plays an important role in the early life of the piranha, Serrasalmus spilopleura in southeastern Brazil. Larvae and early juveniles are found by both day and night among the roots of this free floating waterweed, thus gaining shelter, a rich foraging place, and potential rafting dispersal. Piranha larvae up to 19 mm SL feed mainly on small aquatic arthropods, slowly searched for inside the root tangle; larger juveniles tend to leave the plants and patrol more open areas. At 24 mm SL young piranhas begin to clip out pieces from fins of other fishes and seek shelter in water hyacinths only at night. About 30% of the rafting clumps of water hyacinths may harbour one to three piranha larvae, providing dispersal during floods.