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.     

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.     

Developmental morphology of the cyprinid fish, Candidia barbatus

 Embryonic, larval, and juvenile development of a Taiwanese cyprinid fish, Candidia barbatus, is described from laboratory-reared specimens. The eggs, measuring 1.8–2.1 mm in diameter, were demersal, almost spherical in shape, transparent and unpigmented, with a pale yellow yolk and no oil globule. Hatching occurred 56–69 h after fertilization, the newly hatched larvae measuring 4.9–5.3 mm in body length (BL) with 25–26 + 13–14 = 39–40 myomeres. The yolk was completely absorbed at 7.6 mm BL. Notochord flexion was initiated at 6.8 mm BL and finished at 7.6 mm BL. Aggregate numbers of all fin rays were completed at 12 mm BL. Barbels on the upper jaw appeared near the corner of the mouth at 17 mm BL. Eggs of the species closely resembled those of its related cyprinid genera, Opsariichthys and Zacco. Larvae and juveniles of C. barbatus were similar to those of O. uncirostris subspp., Z. platypus, and Z. pachycephalus, but differed from the latter in the process of disappearance of the adipose finfold (postflexion larval stage), barbels on upper jaw (juvenile stage), and pigmentation on the lateral body surface (postflexion larval and juvenile stages). Although C. barbatus also differed from the Z. temminckii species' group [Z. temminckii and Zacco sp. (sensu Hosoya, 2002)] in having barbels, larvae and juveniles of the former showed more similarity to the latter species group than to O. uncirostris subspp., Z. platypus, and Z. pachycephalus, from the aspect of head and body pigmentation.     

Eggs and larvae of <Emphasis Type="Italic">Awaous melanocephalus</Emphasis> (Teleostei: Gobiidae)

The morphology of eggs and larvae of Awaous melanocephalus is described. The eggs measured 0.33–0.35 mm in long-axis diameter and 0.32–0.34 mm in short-axis diameter. Newly hatched larvae (0.90–0.99 mm in notochord length, NL; 0.93–1.04 mm in total length, TL) were poorly developed, lacking a mouth and having a large yolk sac and unpigmented eyes. The mouth opened and the eyes became fully pigmented 3 days after hatching (1.78–2.00 mm NL, 1.88–2.10 mm TL). The yolk sac was completely absorbed 5 days after hatching at a water temperature of 27°–28°C.     

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.     

Reproductive biology and morphology of eggs and larvae of Stiphodon percnopterygionus (Gobiidae: Sicydiinae) collected from Okinawa Island

Reproductive biology and morphology of eggs and early larvae of the sicydiine goby Stiphodon percnopterygionus were investigated on Okinawa Island, southern Japan. Spawning season was estimated as being from May to December. Standard length at maturity was approximately 20 mm in both sexes, and batch fecundity was approximately 1000–10 000 per female. The egg masses, guarded by the male, were laid on the undersurface of stones in freshwater. The pyriform eggs had long- and short-axis diameters of 0.54–0.58 mm and 0.49–0.50 mm, respectively. Newly hatched larvae (1.20–1.32 mm notochord length: NL) were poorly developed, with large yolk sacs and unopened mouths. Three days after hatching (1.87–2.05 mm NL), eyes were fully pigmented and mouths were opened. An erratum to this article is available at .     

Developmental morphology of the cyprinid fish Horadandia atukorali

Embryonic, larval, and juvenile development of a small Indian cyprinid, Horadandia atukorali, is described from laboratory-reared specimens. The eggs, measuring 0.7–0.8mm in diameter, were demersal, almost spherical in shape, transparent and unpigmented, with a pale yellow yolk without oil globules. Hatching occurred 47–54h after fertilization at 26.3–27.5°C. The newly hatched larvae, measuring 2.3–2.6mm in body length (BL) with 16+13=29 myomeres, had no melanophores, except on the eye, a single melanophore occurring on the lower margin, and xanthophores surrounding the pupil. The yolk was completely absorbed at 3.0mm BL. Notochord flexion was initiated at 4.0mm BL and finished at 4.4mm BL. Aggregate numbers of all fin rays were completed at 8.0mm BL. Squamation was initiated at 6.4mm BL and completed at 9.5mm BL. Although the eggs of Horadandia atukorali resembled those of other small danionin species, including Aphyocypris chinensis, Chela dadiburjori, Danio rerio, Devario malabaricus, and Hemigrammocypris rasborella, they differed from those of Danio rerio and Devario malabaricus in having a narrower perivitelline space. The larvae and juveniles of Horadandia atukorali were also similar to those of the latter five species in general morphology, especially in the presence of a melanophore on the lower margin of the eye at hatching, as in C. dadiburjori. However, the early life stage morphology of Horadandia atukorali differed from the other danionin species in having a conical yolk sac at hatching, no cement organ on the forehead in the yolk-sac larval stage, a divided gas bladder in the flexion larval stage, two dark lateral streaks on the head and chevron-like melanophores on the ventral body surface from the preflexion to postflexion larval stages, and xanthophores on the eyes at hatching.     

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.     

Developmental morphology of the cyprinid fish Chela dadiburjori

Embryonic, larval, and juvenile development of an Indian cyprinid fish, Chela dadiburjori, is described from laboratory-reared specimens. The eggs, measuring 0.7–0.9mm in diameter, were demersal, almost spherical in shape, transparent and unpigmented, with a pale yellow yolk and no oil globule. Hatching occurred 50–61h after fertilization at ca. 27°C. The newly hatched larvae, measuring 2.4–2.6mm in body length (BL), had melanophores on the body with 14–16+14–17=29–31 myomeres. Two dark transverse bands on the ventral body surface and one melanophore on the lower margin of the eye in newly hatched larvae were diagnostic. Additionally, a cement organ for adhering to objects was present on the forehead of yolk sac larvae <3.1mm BL. The yolk was completely absorbed at 3.5mm BL. Notochord flexion was initiated at 5.0mm BL and finished at 6.0mm BL. Aggregate numbers of all fin rays were completed at 9.2mm BL. Squamation was initiated on the caudal peduncle at 8.0mm BL and completed at 10mm BL. The eggs of C. dadiburjori resembled those of the closely related species Devario malabaricus and Danio rerio. The larvae and juveniles of C. dadiburjori were also similar to those of the latter species in general morphology, especially the presence of body melanophores in newly hatched individuals and a distinctive lateral streak on the head during the period from yolk sac to postflexion larvae. However, early yolk sac larvae of C. dadiburjori were more similar to those of Devario malabaricus than Danio rerio in having a cement organ on the forehead. Larvae and juveniles of C. dadiburjori differed from those of the latter two species in pigmentation on the ventral body surface at hatching and around the mouth during the period from preflexion to early postflexion larvae and in having a dark lateral streak or band on the body in postflexion larvae and juveniles.     

Descriptive morphology of the eggs,larvae, and juveniles of two cyprinid fishes belonging to the <Emphasis Type="Italic">Zacco temminckii</Emphasis> species' group

 Embryonic, larval, and juvenile development of two cyprinid species belonging to the Zacco temminckii species' group, Z. temminckii (Temminck and Schlegel) and Zacco sp. (type A), are described and compared with each other from laboratory-reared and wild specimens. The eggs of both species were closely similar except in diameter [1.92–2.20 mm in Z. temminckii vs. 1.60–1.75 mm in Z. sp. (type A)], being demersal, almost spherical in shape, transparent and unpigmented, with a pale yellow yolk, and no oil globule. Hatching occurred 40–53 h after fertilization in Z. temminckii and after 47–60 h in Z. sp. (type A). The newly hatched larvae of both species [4.9–5.3 mm in body length (BL) in Z. temminckii and 3.5–4.8 mm BL in Z. sp. (type A)] also resembled each other, having a large transparent pear-shaped yolk and lacking body pigmentation. Myomere counts of Z. temminckii and Z. sp. (type A) larvae and juveniles were 24–27 + 14–17 = 41–42 and 23–27 + 14–17 = 40–41, respectively. The yolk was completely absorbed at 8.3 mm BL in Z. temminckii and at 6.6 mm BL in Z. sp. (type A). Notochord flexion was initiated and completed at 7.8 mm BL and 8.2 mm BL in Z. temminckii and at 6.3 mm BL and 6.6 mm BL in Z. sp. (type A), respectively. Aggregate numbers of all fin rays were completed at 17 mm BL in Z. temminckii and 13 mm BL in Z. sp. (type A). Although the morphology of larvae and juveniles of both species was very similar, differences in body length of each developmental stage, the duration and process of disappearance of the adipose finfold, the anal fin ray counts, and pigmentation on the lateral body surface were clearly recognized. Received: August 10, 2001 / Revised: March 14, 2002 / Accepted: March 27, 2002     

Embryonic, larval and juvenile development of the roughskin sculpin,Trachidermus fasciatus (Scorpaeniformes: Cottidae)

Embryonic, larval and juvenile development of the catadromous roughskin sculpin,Trachidermus fasciatus, were described using eggs spawned in an aquarium. The eggs, measuring 1.98–2.21 mm in diameter, were light reddish-yellow and had many oil globules, 0.05–0.18 mm in diameter. Hatching occurred 30 days after spawning at 2.3–11.3°C. The newly-hatched larvae, measuring 6.9–7.3 mm BL, had a single oil globule, 9–10+25–26=34–36 myomeres and 6 or 7 large stellate melanophores dorsally along the gut. The yolk was almost resorbed, number of pectoral-fin rays attained 16–17, and two parietal, one nuchal and four preopercular spines were formed, 5 days after hatching, at 8.2–8.4 mm BL. The oil globule disappeared, and one supracleithral spine was formed, 11 days after hatching, at 8.9–9.5 mm BL. Notochord flexion began 15 days after hatching, at 9.7–10.3 mm BL. A posttemporal spine was formed 20 days after hatching, at 10.7–10.9 mm BL. The first dorsal fin spines (VII–VIII), second dorsal fin and anal fin rays (18–19, 16–18, respectively) appeared 23 days after hatching, at 12.0–13.7 mm BL. The pelvic fin spine and rays (I, 4) were formed and black bands on the head and sides of the body began to develop 27 days after hatching, at 13.8–15.8 mm BL. Newly-hatched larvae swam just below the surface in the aquaria. Preflexion larvae (8.9–9.5 mm BL), in which the oil globule had disappeared, swam in the middle layer, while juveniles (13.8–15.8 mm BL) began swimming on the bottom of the aquaria. Swimming behavior observed in the aquaria suggested that the fish started to change to a demersal existence at the juvenile stage.     

Early development of the endangered freshwater goby, Rhinogobius sp. BI (Gobiidae)

The early development of the endangered freshwater goby, Rhinogobius sp. BI (ogasawara-yoshinobori in Japanese), was described in the course of a serial rearing experiment over generations as ex situ preservation. The eggs, measuring 2.0 mm in long diameter and 0.7 mm in short diameter, were elliptical with a colorless transparent chorion, a slightly yellowish yolk, and some oil globules. Hatching occurred naturally at 6 to 7 days after spawning at 24.0°C. Newly hatched larvae, measuring 3.2–3.4 mm in total length (TL), had opened mouth and a globular yolk sac. The yolk was completely absorbed at 3.5 mm TL (5 days after hatching). Notochord flexion initiated at 5.7 mm TL (18 days) and finished at <9.1 mm TL (30 days). First dorsal fin began to form in postflexion larvae at 10.0 mm TL (40 days), and a full complement was attained at 11.6 mm TL (45 days). Second dorsal fin emerged at 5.7 mm TL (18 days); full count was attained and segmentation initiated at 9.1 mm TL (30 days). Anal fin anlage appeared at 5.7 mm TL (18 days); its ray count was completed and segmentation initiated at 9.1 mm TL (30 days), and branching at 15.6 mm TL (60 days). Caudal fin support appeared at 4.5 mm TL (15 days); segmentation initiated at 6.0 mm TL (24 days) and branching at 10.0 mm TL (40 days). Fanlike pectoral fin present in newly hatched larvae. Pectoral fin rays appeared at 10.0 mm TL (40 days), and its ray count completed at 15.6 mm TL (60 days). Pelvic fin projected at 9.1 mm TL (30 days), and a sucking disc partially formed at 11.6 mm TL (45 days). Aggregate numbers of all fin rays were completed at 15.6 mm TL in 60 days after hatching. Pelagic period continued for about 40 days, and settlement was completed in postflexion larvae at 45 days.     

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).     

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

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

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     

Early morphological development ofOmobranchus fasciolatoceps andO. Punctatus (Blenniidae: Omobranchini) reared in an aquarium

Larval and juvenile development of two blenniids,Omobranchus fasciolatocepts andO. punctatus, is described using eggs collected from natural waters in Tokyo Bay and incubated in an aquarium. These larvae and juveniles are compared with those of two otherOmobranchus species,O. elegans andO. loxozonus, distributed widely in Japan.Onobranchus punctatus is characterized by a unique, pointed snout in preflexion larvae, no melanophores proximally on the lower part of the pectoral fins in flexion and postflexion larvae, and pterygiophores projecting externally as blades between the dorsal and anal fin-rays in postflexion larvae and juveniles.Omobranchus fasciolatoceps has the following characteristics: a few melanophores on the fore-and mid-brain, but none on the hind-brain in preflexion larvae; no melanophores on the cleithral symphysis in flexion and postflexion larvae; no external pterygiophore blades in postflexion larvae and juveniles; and a unique dorsal skin flap on the head in juveniles. Ontogenetic developement of dorsal and anal pterygiophores is described forO. fasciolatoceps andO. punctatus. InO. punctatus, the postero-distal part of each proximal radial projects remarkably to form the external blades between the soft fin-rays, whereas the external blades between the fin spines are formed by fusion of a dermal bone developed from the antero-distal part of each proximal radial with the adjacent distal radial.     

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.     

Pelagic eggs and larvae of Coelorinchus kishinouyei (Gadiformes: Macrouridae) collected from Suruga Bay, Japan

Pelagic eggs and larvae of the macrourid fish Coelorinchus kishinouyei, collected from Suruga Bay, southern Japan and subsequently identified by 16S rRNA gene nucleotide sequences, are described. The spherical eggs, 1.18–1.31 mm in diameter, contained a single oil globule, 0.28–0.33 mm in diameter, and had hexagonally patterned ornamentation on the chorion, 0.017–0.022 mm in width. Melanophores were present on the embryo, yolk and oil globule after the blastopore had closed. Within 1 day after hatching, the body axis of the yolk-sac larvae was bent slightly at the anterior trunk region. During this stage many melanophores formed on the head, trunk, tail, yolk and oil globule, along with small irregular wrinkles on the dorsal and ventral finfolds. Pelagic eggs (after the caudal end of the embryo had detached from the yolk) and yolk-sac larvae also developed xanthophores on the embryo and yolk, and head, trunk, dorsal and ventral finfolds just before tail tip, and yolk, respectively. The pelagic larvae had a short tail, stalked pectoral-fin base and no elongate first dorsal and pelvic-fin rays. Three clusters of melanophores were present on the tail (anterior two embedded to muscle and one just before tail tip subsequently lost with development) and a cluster around the anus (beyond 3.9 mm head length). Nucleotide sequence analyses of comparative adult specimens appeared to confirm a previous proposal that C. productus is a junior synonym of C. anatirostris.     

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.     

The eggs and larvae of the giant mudskipper, <Emphasis Type="Italic">Periophthalmodon schlosseri</Emphasis>, collected from a mudflat in Penang,Malaysia

 Eggs of the giant mudskipper, Periophthalmodon schlosseri were collected from a burrow in Penang, Malaysia, in November 1998, and hatched larvae were reared in the laboratory. The eggs were demersal with adhesive filaments and elliptical in shape (0.83–1.43 mm in long-axis diameter). Newly hatched larvae (2.1–2.6 mm in notochord length) possessed a yolk sac. The number of myomeres was 10 + 17 = 27. The mouth and anus were already opened. The larvae started feeding one day after hatching and completely absorbed the yolk by the third day at a water temperature of 24.5–28.0°C. Received: April 9, 2002 / Revised: October 25, 2002 / Accepted: December 10, 2002