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.     

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.     

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.     

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.     

Embryonic and larval traits of the temperate damselfish Chromis crusma reveal important similarities with other Pomacentridae throughout the family's thermal range

Embryonic development and larval morphology of Chromis crusma was described from five nests sampled between 21 and 25 m depth in central Chile (33°S). From each nest, a set of c. 100 randomly selected eggs were hand-collected and transported in seawater to the laboratory. Subsets of c. 30 eggs per nest were maintained in 50 ml glass containers at a constant ambient temperature of c. 12°C (range 11.5–12.9°C). Egg length (L) and width (W) and larval notochordal length (L_N) were measured from photographs. Geometric morphometric analyses were performed in newly hatched and 1 week old larvae to quantify shape changes. Ellipsoid eggs had an average (mean ± SE) size of 1.12 ± 0.05 mm L and 0.67 ± 0.02 mm W, with volume being similar throughout 15 developmental stages (i.e., ellipsoid-shaped; 0.27 mm³). Planktonic larvae hatched between 5 and 11 days at 12°C and had a mean L_N of 3.13 ± 0.25 mm, a yolk sack volume of 0.03 mm³ and an oil droplet volume of 0.005 mm³. Morphological traits at hatching included: (a) lack of paired fins and jaws; (b) single medial fin fold; (c) lack of eye pigmentation; (d) yolk sac present near anterior tip; (e) melanophores distributed along ventral surface with one pair over the forehead. In order to generate an up-to-date summary of developmental traits within Pomacentridae, we reviewed literature on egg development (e.g., shape and number of oil droplets), hatching and larval traits (e.g., morphology, pigmentation patterns). Thirty-two publications accounting for 35 species were selected, where eggs, embryonic development, hatching and larval traits were found for 26, 21, 24 and 34 species, respectively. In order to evaluate potential phylogenetic and environmental relationships within the early stages of Pomacentridae, cluster analyses (Bray Curtis similarity, group average) were also performed on egg and larval traits of 22 species divided by subfamily (Stegastinae, Chrominae, Abudefdufinae, Pomacentrinae) and thermal ranges (i.e., low: 16.5°C (range: 12–21°C), medium: 24.5°C (range:21–28°C) and high: 27°C (range: 26–28°C)), suggesting that early developmental patterns can be segregated by both temperature and phylogenetic relationships.     

Larval ontogeny and morphology of the fire-tailed gudgeon, Hypseleotris galii (Eleotridae)

The larval ontogeny of Hypseleotris galii is described and illustrated. 'Premature' yolk sac larvae hatch with unpigmented eyes and no mouth. 'Late' yolk sac larvae hatch with pigmented eyes and a functional mouth. Hatching glands are distributed on the head and ventral surface of the body. The yolk is absorbed and the larvae begin feeding 6 days after hatching. Larval development is completed 74 days after hatching. Hypseleotris galii larvae have six pairs of naked neuromasts: two pairs on the head and four pairs on the body. The significance of these results to developmental strategies in Hypseleotris species is discussed.     

Development of the cottid fish,Pseudoblennius percoides,reared in the laboratory,with brief descriptions of juvenileP. marmoratus andP. zonostigma

Embryonic, larval and juvenile development of the cottid fish,Pseudoblennius percoides were described on the basis of a series of laboratory-reared specimens. The eggs were demersal, adhesive, almost spherical in shape, measuring 1.66–1.82 mm in diameter, and with numerous various-sized oil globules. Neighboring eggs adhered to each other to form an egg mass. Hatching occurred between 13 and 16 days after spawning at a water temperature of 15.4 to I6.5°C. Newly hatched larvae measured from 6.5 to 7.3 mm, averaging 6.9 mm TL, and possessed 40 myomeres. Absorption of the yolk was completed at about 7.5 mm TL. Flexion of the notochord started and finished at about l0 mm TL and about 14 mm TL, respectively. Aggregate numbers of all fin rays were completed at over 16 mm TL, when the larvae reached the juvenile stage. The pigment pattern became the same as that of adults in juveniles longer than 25 mm TL. Lateral lines were completed at over 44 mm TL, when the juveniles attained to the young stage. The early stages of this species were clearly distinguished from those ofP. cottoides, and the juveniles of fourPseudoblennius species, i.e.P. percoides, P. cottoides, P. marmoratus andP. zonostigma, could be identified mainly by their pigment patterns.     

Development of the bitterling,Tanakia tanago (cyprinidae), with a note on minute tubercles on the skin surface

The development of eggs and larvae and minute tubercles on the skin surface in larvae ofTanakia tanago were observed. The eggs began to hatch approximately 52 hours after insemination and the larvae reached free-swimming stage 19 days after hatching at water temperature of 22±1°C. The egg and larval development and minute tubercles on the skin surface in larvae of this species were similar to those ofAcheilognathus lanceolata andA. limbata. However,T. tanago was distinguishable in egg and larval development fromA. lanceolata andA. limbata by the following characters: the perivitelline space was narrower, embryonic and larval development was faster, and minute tubercles on the skin surface of the anteriormost parts of the yolk sac, and of the body and head were hemispheric in shape. From these characters,T. tanago is considered to be more specialized thanA. lanceolata andA. limbata.     

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,growth and age determination in the sharpnose pufferfishCanthigaster valentini (Teleostei: Tetraodontidae)

The eggs, early larvae and juveniles of the sharpnose pufferfishCanthigaster valentini are described, based on material collected in Great Barrier Reef waters. Eggs were obtained in the field by divers and reared in the laboratory. The eggs are spherical, strongly adhesive, 0.68–0.72 mm in diameter, possess a dense cluster of small oil droplets, and hatch around sunset 3 to 5 days after fertilization. Newly hatched larvae have a small yolk sac, pectoral fin folds, 17 myomeres (6 pre-anal, 11 post-anal) and measure 1.30–1.40 mm in notochord (standard) length. The eggs ofC. valentini differ from those of other tetraodontids in being much smaller and having a longer incubation time. The larvae can be distinguished from other tetraodontid larvae by pigmentation, myomere count and size at hatching. Growth is most rapid during the first day of larval life. Age determinations (based on otolith microstructure) of field collected juveniles, both pelagic and newly settled, indicate a pelagic phase of between 64 and 113 days for this species. This estimate appears consistent with the extended pelagic juvenile stages observed in other tetraodontiform fishes and could indicate thatC. valentini can delay settlement for some time after becoming competent to settle at a minimum age of 64 days.     

Early 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.     

Embryogenesis and larval development of migratory matrinchã Brycon orthotaenia Günther 1864 (Characiformes: Bryconidae)

The present study aimed to characterize the embryogenesis and larval development of matrinchã (Brycon orthotaenia), through the analysis of egg and larval morphology. Fertilized eggs had a mean diameter of 1.17 mm, with yolk occupying most of the egg (1.06 mm). Embryogenesis lasted for 15 hr at an average temperature of 27°C. At hatching, yolk-sac larvae measured 3.67 mm in mean standard length (SL). Pre-flexion, flexion and post-flexion larva had 5.01, 8.24 and 11.88 mm mean SL, respectively, with significant increases observed particularly in head length, head height, and eye diameter. The yolk persisted in the yolk-sac and pre-flexion stages (5.96 mm SL). The mouth opening could first be observed 13 hr after hatching, and cannibalism was observed 29 hr after hatching in pre-flexion larvae after absorption of the yolk sac; in such cases, the larvae had already developed teeth and a complete digestive tract. For an endangered species such as matrinchã, early life history studies are important because they provide researchers with a better understanding of critical stages of development and thus enhance captive management by rearing and restocking of the species.     

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.     

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.     

Induction of ovarian maturation and development of eggs,Larvae and Juveniles of the Puffer,Takifugu exascurus,Reared in the Laboratory

Ovarian maturation of the pufferTakifugu exascurus (Jordan et Snyder) was induced, and embryonic, larval and juvenile development was observed. The brood fish were collected in Tassha Bay, Sado Island (38°05′N, 138°15′E), during the spawning season in 1986 which seemed to extend from late June to mid-July. To each female 3 mg acetone-dried pituitary ofHypophthalmichthys molitrix was injected to induce ovarian maturation, which took place in about 77 hours at a water temperature of 19.5–21.0°C. The eggs obtained by hormone injection were artificially fertilized with the milt from a collected male. The hatched larvae were fed successively on rotifersBrachionus plicatilis, Artemia nauplii and minced fish meat, and reared for a period of about one year. The eggs were spherical, 1.24±0.04mm in diameter, demersal and adhesive. The egg-membrane Was transparent and yolk was orange in color, containing a cluster of small oil-globules. The incubation period was about 160 hours at a water temperature of 18.5–21.0°C. The newly-hatched larvae, measuring 2.9– 3.1 mm TL, had 8+15 = 23 myomeres. Absorption of the yolk was completed 3 days after hatching, by which time the larvae had attained 3.5–3.6 mm TL. Larval finfolds disappeared and rudimentary dorsal, anal and caudal fins formed at 4.1–4.4 mm TL, in 6 days after hatching. In 9-day old larva (5.4 mm TL), fin ray rudiments appeared on the dosai, anal and caudal fins and spine-like scale formed on the belly. In 16-day old specimens, 9.1–10.2 mm TL, the full complements of fin rays were completed on all the fins and the fish reached the juvenile stage. The growth of larvae and juveniles reared in 1986–1987 is expressed by the following equations, where y is total length (mm) and x is days after hatching. y₁ = 2.9420· 1.0639^x 0 ≦ x ≦ 19 (r = 0.998) y₂ = 4.0286· 1.0464^x 19≦ x ≦ 33 (r = 0.998) y₃ = 9.8854· 1.0180^x 33 ≦ x ≦ 72 (r = 0.996) y₄ = 20.1555· 1.0080^x 72 ≦ x ≦ 115 (r = 0.998) y₅ = 28.0610· 1.0049^x 115 ≦ x ≦ 202 (r = 0.995)     

Spawning habitat and early development of Luciogobius ryukyuensis (Gobiidae)

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

Embryonic development and newly hatched larvae of the little dragon sculpinBlepsias cirrhosus

This paper describes both embryonic development and newly hatched larval morphology of the little dragon sculpinBlepsias cirrhosus. The eggs ofB. cirrhosus are almost spherical, 3.0–3.2 mm in diameter, and have a yolk color of burnt orange. Development is very slow, being especially sluggish once the embryo appears. The embryo begins forming from the 10th day. In size, the early embryo is less than 1/6 of the yolk’s circumference. Incubation at 10°C takes about 200 days, 50 days shorter than the incubation period in a natural environment, with a mean water temperature of 11°C. The notochord length of newly-hatched larvae averages 11.1 mm. The larvae are developed so fully that the notochord is already flexing and the caudal and pectoral rays are forming.     

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.     

Comparative Prey Suitability ofOstrinia nubilalisEggs andAcyrthosiphon pisumforColeomegilla maculata

The effects ofOstrinia nubilalis(Hübner) (Lepidoptera: Pyralidae) eggs andAcyrthosiphon pisum(Harris) (Homoptera: Aphididae), when provided as single prey species and in combination, on life history characteristics ofColeomegilla maculataDeGeer (Coleoptera: Coccinellidae) larvae and adults were quantified. Preimaginal development was not influenced by the larval prey regime; development at 26 ± 1°C was completed in approximately 13.5 days onO. nubilaliseggs,A. pisum,orA. pisumalternated daily withO. nubilaliseggs. The resulting adults weighed 13.0, 10.7, and 12.5 mg when reared onO. nubilaliseggs,A. pisum,andA. pisumalternated daily withO. nubilaliseggs, respectively. Eighteen percent of the individuals died when reared onA. pisum,28% died when reared onO. nubilaliseggs, and 22% died when fedA. pisumalternated daily withO. nubilaliseggs. Seven adult diet combinations, based on diet regimes of larvae and adults, did not cause significant differences in preoviposition period, interoviposition period, and the number of days on which eggs were laid. Total fecundity was influenced both by larval and adult diet. The diet that resulted in highly fecund females wasA. pisumalternated daily withO. nubilaliseggs for larvae andO. nubilaliseggs for adults. FemaleC. maculatafedO. nubilaliseggs had the highest intrinsic rate of increase and net reproductive rate.