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A total of 148 specimens of Mitsukurina owstoni were examined for morphology, distribution, stomach contents, and reproductive condition. Sixty-nine males (81.7–208.5 cm in total length, TL) and 56 females (92.8–196.1 cm TL) were collected with bottom gillnets along a steep slope of the Tokyo Submarine Canyon (100–350 m depth) from May 1995 to October 1996. In addition, data were obtained from 23 specimens of M. owstoni collected from Sagami Bay, Suruga Bay, and the Enshu-nada Sea from 1972 to 2001. Japanese catch records already published (from 1898) plus those in the present study were from the Pacific coast of Japan, from Choshi to the Kii Peninsula. The main fishing season for M. owstoni by bottom gillnet fishing in the Tokyo Submarine Canyon was October to April, at depths of 200–245 m. No specimens examined were sexually mature, including the largest male (208.5 cm TL) and female (196.1 cm TL) recorded. Of 110 stomachs from specimens from the Tokyo Submarine Canyon, 32 (29.1%) were empty. The remainder variously included teleost fishes, squids, decapods, isopods, digested food, and human refuse. Teleost fishes (Macrouridae sp. and Stomiidae spp.), an isopod (Cymothoidae), and decapods (Pasiphaea sinensis and Sergia sp.) were the only identifiable prey, the indication being that teleosts (all size ranges) were of primary importance as prey for M. owstoni.

Past treatments of the sleeper shark genus Somniosus generally recognize three species: S. microcephalus, S. pacificus, and S. rostratus. Based on morphometrics and meristics, we conclude that this genus includes two subgenera (Somniosus and Rhinoscymnus) and five species. Subgenus Somniosus differs from Rhinoscymnus by being much larger when adult and in having more numerous tooth rows in the lower jaw, hooklike rather than leaf-shaped dermal denticles, more numerous spiral valve and vertebral counts, and a poorly calcified vertebral column. Subgenus Somniosus includes S. (Somniosus) microcephalus and S. (S.) pacificus of the Northern Hemisphere and S. (S.) antarcticus of the Southern Hemisphere. Although Somniosus antarcticus has been synonymized with S. microcephalus and identified as S. pacificus in past literature, it differs from S. microcephalus in having a shorter interdorsal space, a more posterior first dorsal fin, lower dorsal fins, more numerous tooth rows in the lower jaw, more numerous spiral valve counts, and fewer precaudal vertebrae. Somniosus antarcticus also differs from S. pacificus by having a shorter prebranchial length, lower dorsal fins, more numerous spiral valve counts, and slightly more precaudal vertebrae. Subgenus Rhinoscymnus includes S. (Rhinoscymnus) rostratus from the eastern North Atlantic and Mediterranean Sea (senior synonym of S. bauchotae) and S. (R.) longus from the western Pacific Ocean. Somniosus longus has been synonymized with S. rostratus, but differs in having a relatively longer second dorsal fin, a slightly larger eye, more lower tooth rows, and slightly higher spiral valve counts. Both Somniosus (Somniosus) antarcticus and S. (Rhinoscymnus) longus from the Pacific Ocean were redescribed. A key to the species and the geographical distribution of all species are provided.

The viper dogfish, Trigonognathus kabeyai is further described on the basis of 19 male [176–470 mm in total length (TL)] and 13 female (325–539 mm TL) specimens collected from the Kumano-nada Sea. In addition, the holotype, paratype, and seven specimens collected from the stomachs of Taractichthys steindachneri and Thunnus obseus from the Ogasawara Islands, Japan, were also examined. This is the first description of large (adult) specimens. The allometric size-on-size equation Y = aX b was used to determine morphometric growth patterns, positive allometry, negative allometry, and isometry. Size at maturity was about 430 mm TL for males and about 520 mm TL for females. Myctophid fishes consisting of Diaphus gigas, Diaphus spp., Benthosema fibulatum, and Benthosema sp. were the only identifiable prey in the stomachs of Trigonognathus kabeyai examined. Most of the prey fishes were found almost intact and usually had puncture holes made by teeth. On the basis of stomach content and jaw morphology, this species is thought to be a ram feeder.

On 11 July 1997, the mating behavior of wild manta rays,Manta birostris, was observed while skin diving off Chichijima. Ogasawara Islands, Japan, and recorded with 49 underwater photographs and about 20 minutes of video tape. The female manta ray involved was estimated as being approximately 5 m in dise width (DW) and the two males involved, approximately 4 m DW. Copulatory behavior of the two males appeared to be almost the same, copulation itself being of the abdomen-to-abdomen type. Initially, the males chased the female for 20–30 minutes, all animals swimming at approximately 10 km/h. Each copulation event occurred within one meter of the surface, during which time the participating male grasped the tip of the female's left pectoral fin with his mouth. The clasper was inserted for 90 seconds (Male No. 1) and 60 seconds (Male No. 2), respectively. The mating behavior sequence of the manta rays involved following five steps. 1.: Male chases behind the tail of the female, attempting (several times) to grasp the latter's pectoral fin (chasing behavior). 2.: Male bites the tip of the female's pectoral fin, before positioning itself against the latter's underside (biting behavior). 3.: Male inserts a clasper into the cloaca of the female (copulating behavior). 4.: Male removes the clasper from the cloaca of the female, but continues biting the latter's pectoral fin (post-copulating behavior). 5.: Male releases the pectoral fin of the female, setting her free (separating behavior).

Specimens of the brown lanternshark,Etmopterus unicolor, reported here for the first time from the waters around New Zealand, were caught on bottom longlines. This study compares morphometeric and meristic characters of New Zealand and Japanese specimens ofE. unicolor and New Zealand specimens of the southern lanternshark,E. granulosus. E. unicolor andE. granulosus are clearly distinguishable by the height of the first dorsal fin, number of spiral valves, number of vertebrae, and shape of the dermal denticles and teeth.

A new species of the lanternshark Etmopterus splendidus is described. This new species is distinguished from the congeners by the combination of the following characters: distance from snout tip to 1st dorsal spine much less than distance from the spine to upper caudal origin; caudal fin short, much less than head length; dermal denticles on lateral side of trunk with very small, erect thornlike, conical crowns, those on trunk arranged in regular longitudinal rows, and distinctly arranged on interdorsal area and on lateral trunk of interspace between 2nd dorsal and caudal, but not arranged in regular longitudinal rows on dorsal surface of interorbital and o abdomen; color in life purplish-black above and with inconspicuous bluish-black flank marks and three other bluish-black marks at base of caudal fin and along its axis; shape of flank marks narrow anterior to, but broader posterior to pelvic fins.