Development of Sebastes taczanowskii (Scorpaenidae) in the Sea of Japan off Hokkaido with a key to species of larvae

The larval and juvenile stages of Sebastes taczanowskii (Japanese name: Ezo-mebaru) are described and illustrated based on 33 wild specimens [7.1–26.9 mm in body length (BL)] collected in the Sea of Japan, and eight specimens of reared larvae extruded from the one specimen of a captive pregnant female. Larvae were extruded between 4.3–5.0 mm BL and notochord flexion occurred 5.7–9.0 mm BL. Transformation from postflexion larvae to pelagic juveniles occurred between 13 and 17 mm BL. Preflexion and flexion larvae have a single melanophore row on the dorsal surface on the tail, and an internal line of melanistic dashes on the ventral side of the tail. Lateral pigmentation of postflexion and transforming larval body surfaces are light. Compared with other Japanese rockfish species, S. taczanowskii is shallow-bodied throughout both larval and juvenile stages. We provide an identification key to preflexion and flexion stage rockfish larvae found around the Japanese archipelago, and comparisons with other species. Larval and juvenile S. taczanowskii occurred in both near-shore and relatively offshore water around Shakotan Peninsula-Ishikari Bay, Hokkaido in June and July.     

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.     

Shrinkage of Prochilodus lineatus (Valenciennes, 1847) larvae preserved in either ethyl‐alcohol or formalin in relation to their developmental stage and feeding condition

The effects of preservation in 95% ethyl‐alcohol and 5% formalin were analysed for 3 months on standard length of Prochilodus lineatus larvae from hatching to the end of the flexion process. Unyolked stages were raised under two feeding regimes: unfed and daily fed. All developmental stages that were preserved in formalin as well as the yolked and flexion‐postflexion larvae stored in alcohol shrank significantly (2–6%). In contrast, unyolked preflexion larvae showed a slight but significant enlargement after storage in alcohol (1%). Shrinkage of preflexion stages was 2.5% higher when stored in formalin, while both preservative agents caused similar shrinkage in flexion‐postflexion larvae (ca. 3%). Shrinkage levels after storage in alcohol were dependent on live length, decreasing or increasing with increasing length in yolked and flexion‐postflexion larvae, respectively. The feeding regime did not affect length changes after preservation in either preservative agent.     

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.     

Early life history of mebaru,sebastes inermis (scorpaenidae), in sendai bay, japan

The early life history of the viviparous scorpaenid,Sebastes inermis, in Sendai Bay, Japan, was studied and early development described. Newborn preflexion larvae ofS. inermis were about 5.2 mm BL. Notochord flexion occurred at 5.4–8.0 mm BL and transformation at 14–20 mm BL. Preflexion and flexion larvae ofS. inermis were distinguished from similar larvae by the pigmentation pattern along the dorsal and ventral midlines of the tail. Pigmentation inS. inermis was light throughout the larval and early juvenile periods. Planktonic larvae were particularly abundant in coastal waters of Sendai Bay but not offshore. Vertical and horizontal larval sampling indicated that early larvae occupied near surface waters and horizontal larval sampling indicated that early larvae shift to a benthic habitat occurred at about 12 mm BL, at the end of the postflexion larval period.Sebastes inermis do not have a distinct pelagic juvenile stage, unlike many North Pacific species ofSebastes.     

Developmental morphology of the Indian cyprinid fish Barilius canarensis

Embryonic and larval development of an Indian cyprinid fish, Barilius canarensis, is described from laboratory-reared specimens. The eggs, measuring 2.1–2.4 mm in diameter, were demersal, almost spherical in shape, transparent and unpigmented, with a pale yellow yolk without oil globules. Hatching occurred 39–45 h after fertilization at 26.8°–27.4°C. The newly hatched larvae, measuring 4.8–5.1 mm in body length (BL) with 22 + 17 = 39 myomeres, were characterized by melanophores already deposited on the eyes. The eggs of B. canarensis resembled those of the related danionin species Candidia barbatus, Opsariichthys uncirostris uncirostris, Zacco platypus, Z. sieboldii, and Z. temminckii. Although the larvae of B. canarensis were also similar to those of the foregoing species in general morphology, they differed in having a straight notochord tip and pigmentation on the eyes at hatching and the almost entire absence of melanophores on the ventral body surface from the yolk sac to postflexion larval stages. Conversely, melanophores occurred on the anterior abdominal and pericardial cavities from the preflexion to postflexion larval stages.     

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.     

Larval development of two species of barracuda,Sphyraena guachancho andS. tome (Teleostei: Sphyraenidae), from southeastern Brazil

Morphological development of barracudas (Sphyraena guachancho andS. tome) is described, based on larval and juvenile specimens collected in the southeast Brazilian Bight. Preflexion larvae of the two species are similar, butS. tome larvae can be distinguished from those ofS. guachancho by having small melanophores on the midbrain and a row of melanophores along the ventral midline of the lower jaw and isthmus. Flexion and postflexion larvae ofS. tome are more slender than those ofS. guachancho. Morphology and pigment patterns ofS. tome are similar to those ofS. borealis from the north Atlantic. whereasS. guachancho larvae are similar toS. barracuda in having a fusiform body, advanced position of the pelvic fins and a heavily pigmented tail region, but differ in having a fleshy tip on the lower jaw in postflexion and juvenile stages.     

Developmental morphology of the cyprinid fish Inlecypris auropurpureus

Embryonic, larval, and juvenile development of a Myanmarese cyprinid fish, Inlecypris auropurpureus, is described from laboratory-reared specimens. The eggs, measuring 0.9–1.0 mm in diameter, were demersal, almost spherical in shape, transparent and unpigmented, with a pale yellow yolk without oil globules. Hatching occurred 49–56 h after fertilization at 26.2°–27.3°C. The newly hatched larvae, measuring 2.9–3.1 mm in body length (BL) with 17 + 19–20 = 36–37 myomeres, had melanophores on the head and body. A cement organ on the forehead for adhering to objects during the yolk sac and early preflexion larval stages was distinctive. The yolk was completely absorbed at 3.6–4.0 mm BL. Notochord flexion was initiated at 5.1–5.6 mm BL and finished at 7.1 mm BL. Aggregate numbers of all fin rays were completed at 14 mm BL. Squamation was initiated midlaterally on the anterior trunk at 14 mm BL and completed at 27 mm BL. Although the eggs of I. auropurpureus resembled those of the closely related species Chela dadiburjori, Danio rerio, and Devario malabaricus, they differed from those of Danio rerio and Devario malabaricus in having a narrower perivitelline space. The larvae and juveniles of I. auropurpureus were also similar to those of C. dadiburjori, Danio rerio, and Devario malabaricus in general morphology, but they differed from the latter three species in having a series of dark blotches laterally on the body in the juvenile stage. Moreover, I. auropurpureus differed from C. dadiburjori in having more myomeres and a near-single row of melanophores on the body along the dorsal midline from the yolk-sac to early postflexion larval stages, from Danio rerio in having a cement organ on the forehead during the yolk-sac and early preflexion larvae, and a single melanophore on the lower eye margin in the early yolk-sac larvae, and from Devario malabaricus in having a single melanophore on the lower eye margin in the early yolk-sac larvae. The presence of a cement organ on the forehead indicates a close relationship among the genera Inlecypris, Chela, and Devario.     

Early life history of kitsune-mebaru,sebastes vulpes (scorpaenidae), in the sea of japan

The larval and juvenile stages of kitsune-mebaru,Sebastes vulpes, based on 50 wild specimens collected in, the Sea of Japan, are described and illustrated, and some ecological aspects of the early life history (feeding, horizonal distribution and habitat shift) included. Preflexion larvae became extruded between 3.9–4.6 mm body length (BL) and notochord flexion occurred between 4.7–7.1 mm BL. Transformation from postflexion larvae to pelagic juventiles occurred between 13–17 mm BL. Compared with other rockfish species,S. vulpes is deep-bodied, throughout both larval and, juvenile stages. Larval and juvenileS. vulpes inhabit mainly coastal water surface layer (usually on the continental shelf), but do not occur offshore region (northwest of Oki Islands). Although someS. vulpes juveniles are associated with drifting seaweed, such clumps are not indispensable habitats for any stages. Surface-to-benthie migration of juveniles occurs at about 25 mm BL. Preflexion and flexion larvae feed mainly on copepod nauplii, and postflexion, transforming larvae and pelagic juveniles mainly on calanoid copepodites (Parracalanus parvus).     

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.     

Larval development of Asemichthys taylori (Cottidae)

Larvae of Asemichthys taylori were reared in the laboratory to identifiable juveniles. A preserved series of larvae was characterized in part by fin meristics (X–XI, 14–15 dorsal fin rays; 15 anal fin rays), as well as a combination of the alignment of the jaw tip with the ventral margin of the gut, heavy lateral melanistic pigment except on the caudal peduncle, and a series of postanal ventral melanophores. An internal, horizontal band of melanin extends through the head from the snout to the gut. Hypural plates do not align vertically even after settlement, giving the appearance that the larvae do not complete notochord flexion during their planktonic stage. Larval A. taylori resemble known larvae of Radulinus spp., a genus under which some authors have synonymized the monotypic genus Asemichthys.     

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.     

Developmental morphology of the cyprinid fish Tanichthys albonubes

Embryonic, larval, and juvenile development of a small cyprinid species, Tanichthys albonubes, is described from laboratory-reared specimens. The eggs, measuring 1.0–1.2 mm in diameter, were demersal, almost spherical in shape, transparent and unpigmented, with a pale yolk without oil globules. Hatching occurred 45–53 h after fertilization at 25.5°–26.9°C. The newly hatched larvae, measuring 2.2–2.6 mm in body length (BL), had melanophores on the head and body. In particular, a dark vertical streak occurring posterior to the otic capsule and melanophores above the eyes were distinctive. The yolk was completely absorbed at 3.4 mm BL. Notochord flexion was initiated at 5.0 mm BL and finished at 6.0 mm BL. Aggregate numbers of all fin rays were completed at 11 mm BL. Squamation was initiated at 8.4 mm BL and completed at 13 mm BL. Although the eggs of T. albonubes resembled those of other small danionin species, including Aphyocypris chinensis, Chela dadiburjori, Danio rerio, Devario malabaricus, Gobiocypris rarus, Hemigrammocypris rasborella, and Horadandia atukorali, they differed from those of A. chinensis, C. dadiburjori, G. rarus, and Horadandia atukorali in having a wider perivitelline space. The larvae and juveniles of T. albonubes were similar to those of the aforementioned seven species plus Danio albolineatus, Danio kerri, and Devario sp. (cf. D. aequipinnatus) in general morphology. However, the early life stage morphology of T. albonubes differed from them in having a dark vertical streak posterior to the otic capsule and melanophores above the eyes in the yolk sac larval stage, and a dark lateral streak with an unpigmented area just above the former on the body, a dark blotch on the caudal fin, and reddish dorsal, anal, and caudal fins during the postflexion larval and juvenile stages.     

Systematics and identification of larvae and juveniles of the genusSebastes

Synopsis Current information on systematics and morphology of larvae and juveniles ofSebastes is reviewed, as are intrageneric relationships among the many species of the genus. Although some subgenera may remain after a cladistic analysis of the genus, others are probably artificial groupings of species that have convergent morphologies because of similar ecology. The relationships ofSebastes to other scorpaeniform fishes as well as the relationships of scorpaeniforms to other fishes are not resolved. Of the 102 species ofSebastes worldwide, 69 species have been illustrated as preflexion larvae, 35 as postflexion larvae and 65 as pelagic juveniles. Morphological characters of each of these stages were used to compare species, group them by similar appearances and then compare these groupings with existing subgenera. Some pigment patterns of preflexion larvae were rather consistent among species within certain subgenera but quite variable among species in other subgenera. Postflexion larvae fell into 11 groups based on pigment, head spines and body shape. These groups were not closely aligned with the subgeneric assignments of the component species. On the basis of pigment patterns of pelagic juveniles, six groups were evident, but the specific composition of these groups bore little resemblance to either the larval or subgeneric groups.     

Larval development of bigmouth manefish Caristius macropus (Perciformes: Caristiidae) from the western North Pacific

Larvae of bigmouth manefish Caristius macropus are described and illustrated on the basis of seven specimens (4.2–10.5 mm in body length) from the Kuroshio waters (0–60 m depth) and the transition waters (surface) between the Kuroshio and Oyashio fronts of the western North Pacific. The present larvae of C. macropus are distinguished from those of Paracaristius maderensis that inhabit the North Pacific by having 39–40 myomeres, 34 dorsal-fin rays, and 22 anal-fin rays. The present study, along with previous studies of the early life stages of caristiids, shows that larvae of the family may be defined by the following characters: body elongate in preflexion stage but becoming deep bodied and hatchet shaped after notochord flexion; anus located near vertical through base of pectoral fin; head large, without spination or serration; a distinct vertical band on the posterior tail throughout the larval stages, and two bands gradually appearing on the tail and trunk during the flexion and postflexion stages; and melanophores present around the notochord tip by the flexion stage. Adult C. macropus are found in the subarctic and temperate waters of the North Pacific; however, the present study and other occurrences of early life stages of the species probably indicate that C. macropus may spawn over a wide area in the North Pacific.     

Occurrence of Ayu (<Emphasis Type="Italic">Plecoglossus altivelis</Emphasis>) larvae in northern Vietnam

The early life history of Ayu (Plecoglossus altivelis) was investigated in the Kalong and Tien Yen River systems, northern Vietnam, which is probably the most southern distribution locality for this species, during the period of November 2010 to February 2011. A total of 248 larvae were captured in the Kalong, and none were collected in the Tien Yen. There was little difference in development between the Kalong larvae and those of P. a. altivelis and P. a. ryukyuensis. Temperatures and salinities when the larvae were collected ranged from ca. 12 to 21°C and from ca. 3.5 to 30 psu. The preflexion to flexion larvae (primarily preflexion with yolk, 5.2–12.9 mm BL) occurred in the central current from December to February, with a peak abundance in early January. The flexion to postflexion (primarily postflexion, 14.1–23.8 mm BL) larvae occurred in the bank waters from early January to late February. The larval occurrence in the Kalong was 1–2 months later than for P. a. altivelis in Japan and P. a. ryukyuensis in the Ryukyu Islands, probably because of the delay until a reasonable photoperiod for the start of spawning in the lower latitudinal region. The larvae were never collected from the sea, where the temperatures were lower than in the river and estuary in January and February, unlike in Japan.     

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.     

Early ontogeny of Lophonectes gallus (Bothidae) from southeastern Australia

 The early ontogeny of Lophonectes gallus (Bothidae) is described based on 83 specimens (1.9–17.5 mm BL), collected from the Tasman Sea off southeastern Australia. The larvae are diagnosed by the following array of characters: vertebrae 10 + 30–31 = 40–41; one elongated dorsal fin ray and several melanophores present on gut in preflexion stage (1.9–4.7 mm BL); and spines on posterior basipterygial process, and urohyal, cleithrum, and epiotic without spines after postflexion stage (8.0–17.5 mm BL). The larvae are relatively small at metamorphosis (15–18 mm BL) compared with other bothid larvae. Received: March 22, 2001 / Revised: December 12, 2001 / Accepted: December 26, 2001