Japanese Journal of Ichthyology
Online ISSN : 1884-7374
Print ISSN : 0021-5090
ISSN-L : 0021-5090
Volume 21, Issue 2
Displaying 1-7 of 7 articles from this issue
  • Ryoichi Arai, Hiroshi Hirano
    1974 Volume 21 Issue 2 Pages 53-60
    Published: November 30, 1974
    Released on J-STAGE: June 28, 2010
    JOURNAL FREE ACCESS
    Nine specimens of a clariid catfish, Clarias frtscus.which is new to Japan, were collected at Ishigaki Island, the southern Ryukyus.Characteristics of these specimens are described, with special reference to differences among Clarias fuscus. C.hatrachus.and C.macrocephalus.Variations of characters are investigated in28 specimens of Clarias fuscus from Japan.Formosa, and Philippines.The diploid chromosome number of the species is 56, and the karyotype is described.
    Download PDF (4609K)
  • Shyohei Nishikawa, Kunio Amaoka, Kazue Nakanishi
    1974 Volume 21 Issue 2 Pages 61-71
    Published: November 30, 1974
    Released on J-STAGE: June 28, 2010
    JOURNAL FREE ACCESS
    Karyotypes of12species (in 9 genera, 5 subfamilies, 2 families) of Japanese gobioid fishes were examined.The ranges are44-50in diploid number and44-96 in arm number.The diploid numbers of33species and2subspecies including those that have already been reported, show no clear relationships at the subfamily level of the current classification, though they are well stabilized at generic level.Among genera examined, Odontobutis and Rhinogobius have the simplest karyotype, and Acanthogobius, Chasmichthys, Tridentiger, Chaenogobius, Boleophthalmus, Periophthalmusand Acentrogobius follow in due order.
    Download PDF (10623K)
  • Prince Akihito, Katsusuke Meguro
    1974 Volume 21 Issue 2 Pages 72-84
    Published: November 30, 1974
    Released on J-STAGE: July 04, 2011
    JOURNAL FREE ACCESS
    Ophieleotris aporos was originally described by Bleeker (1854: 59) as Eleotris aporos.After Gill (1863: 270) established the genus Ophiocara based on Eleotris ophicephalusValenciennes, a synonym of Ophiocara porocephala (Valenciennes), E.aporos wasassigned to the genus Ophiocara by Bleeker (1877: 27).Aurich (1938: 132) established a new genus Ophieleotris for O.aporos based on the study of sensory canal pores, arrangement of pit organs and other characteristics. However, his genus has not been used by others but Whitley (1964: 55), as far as it is known to us.
    Our study on comparative morphology on O.porocephala and O.aporos with other species, listed on p.74, has revealed further different characteristics between two species and other species, some of which can be used for separating O.aporos from the genus Ophiocara and for recognizing the genus Ophieleotris for O.aporos.
    The characteristics of the two species are listed in Table 1.The most importantcharacteristics of the two genera, Ophiocara and Ophieleotris, in comparison with othergenera listed on p.74 are: 1) The presence of a process on the inner side of themaxillary in Ophiocara (Fig.1A) and the absence in Ophieleotris (Fig.1B).2) Thepresence of oculoscapular canal from nasal to posttemporal with the pores A to Lexcept for G, of preopercular canal with the pores M to Q and three supratemporalsin Ophiocara (Fig.2A);the absence of oculoscapular canal and supratemporals andthe presence of short preopercular canal with the pores N'and O'in Ophieleotris (Fig.2B). 3) 17 segmented caudal fin rays in Ophiocara and 15 segmented caudal finrays in Ophieleotris.4) 26 (or rarely 27) vertebrae and the first and second pterygiophoresof the first dorsal fin are inserted between the third and fourth vertebrae in Ophiocara (Fig.3A);25 vertebrae and the first pterygiophore between the third and fourthvertebrae (Fig.3B) or the first two or three pterygiophores between the fourth andfifth vertebrae in Ophieleotris (Fig.3C).5) The presence of a short, low longitudinalridge on frontal in Ophieleotris (Fig.4A);the absence of the ridge in Ophiocara (Fig.4B).6) The size of a scale of interorbital space of Ophiocara smaller than thatof caudal peduncle;the size of a scale of interorbital space of Ophieleotris larger thanthat of caudal peduncle and the largest of all the genera;the size of a scale of caudalpeduncle of both genera is not different.Although O. porocephala has no suborbitalwhose presence is thought to be an unspecialized characteristic, it has common characteristicsin 1) to 4) with the species with a suborbital, except for the loss of thepore G.Thus O.porocephala closely resembles the species with a suborbital whichare thought to be the most unspecialized species. As for O.aporos, when compared with them, it has no characteristics which are as unspecialized as those found in O.porocephala.
    Download PDF (2287K)
  • Seirô Kimura
    1974 Volume 21 Issue 2 Pages 85-91
    Published: November 30, 1974
    Released on J-STAGE: July 04, 2011
    JOURNAL FREE ACCESS
    A spawning redd of the salmonid fish was found in the Nigorimizu-sawa of the Oirase River system (40° 41'N, 139°58'E), which flows into the Japan Sea in Aomori Prefecture (Figs.2, 3).More than 1, 700 eyed eggs were obtained on November 21, 1960, from this redd.These eggs measured 5.3-5.9mm in diameter.They began to hatch on November 24.The alevins and fry are described and illustrated in this paper (Fig. 4).The fry, liberated in a small pond (ca.4 m2, 50-80 cm deep), took mainly small crustacea and aquatic larvae of insects and attained 38 43 mm in total length by the next April.These fry are considered as members of either of the genera Salvelinus or Hucho for their characteristic arrangement of the vomer and palatine in the roof of the mouth (Fig.5).Because the fish of Hucho is a vernal spawner in Japan, the present fry must belong to Salvelinus.
    In the Nigorimizu-sawa, there are two types of char Salvelinus leucomaenis (Pallas), i.e., an anadaomous form and a fluvial dwarf form of the same species.Generally, the former grows up 40 cm or more in total length, however, the latter attains 30 cmat largest and rarely deposits eggs exceeding 300 in number at a single spawning redd.Therefore, the present spawning redd, eggs, alevins, and fry are thought to be of theanadromous char called“Amemasu”in Japanese (Fig.1).The parr marks appear inthe alevins of S.malma (Walbaum) (Blackett, 1968), but not visible in the presentalevins throughout their yolk consuming stage (Fig.4).So, there is no reason toidentify these alevins as S.malma.
    Download PDF (7528K)
  • Taketo Fujii
    1974 Volume 21 Issue 2 Pages 92-100
    Published: November 30, 1974
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
    Among platycephalid fishes, transition on sexuality from hermaphroditism to gonochorism is recognized paralleled with the patterns of morphological changes of gonads accompanied by protandrous sex reversal.Here, the speciation of platycephalid fishes was reexamined on the basis of the taxonomic study of Matsubara and Ochiai (1955), considering a few additional characters.As a result, it became clear that declination of the hermaphroditic nature corresponds to the process of the speciation.
    Generally two directions were recognized in this process;one is toward specialization and gave rise to fishes of the subfamily Onigociinae, and another is toward largesize and brought about the subfamilies Inegociinae and Platycephalinae.It was considered that the genus, Kumococius, lies at the center of speciation of these groups, since the species of this genus retains a few relic characters of nektonic life, such as absence of the nasal flap;the slightly concave pectoral fin along the posterior margin; and small, less degenerated gas bladder.As species become more specialized, hermaphroditism tends to decrease.From this, the ancestor of the platycephalid fishes might be considered synchronously hermaphroditic carrying a marked hermaphroditic nature.
    It is known that the transitional trend from hermaphroditism to gonochorism also exists in the Serranidae and Sparidae, as well as in the Platycephalidae.Structures of representative hermaphroditic gonads of these families are judged to be similar to that of synchronous hermaphrodite, as well as the Serranidae.From this it was considered that hermaphroditism of at least these three families have a common evolutional foundation and that hermaphroditism might have been the original condition in these fishes.
    Download PDF (1305K)
  • Hirokazu Kishimoto
    1974 Volume 21 Issue 2 Pages 101-107
    Published: November 30, 1974
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
    In May 11th, 1973, 399 specimens of Stethojulis were collected in Suruga Bay, ofwhich 33 showed color phase of S.interrupta and 366 that of S.kalosoma.In anaquarium, 312 specimens with“kalosoma”pattern were kept at the water temperature18.3-25.1°C.Some of them changed their color pattern to“interrupta”phase, within10 days.Among 312 specimens, 54 (42 died, 12 alive) changed to S.interrupta phaseand 258 remained in“kalosoma”phase (187 died, 71 alive), by July 31, 1973.Duringthe color change, certain specimens took on color patterns resembling S.“trossula”.It was found that individuals of“kalosoma”phase included female, male and indeterminables, whereas those of“interrupta”phase were all males.On the basis ofmorphological characters and color patterns, it was concluded that S.kalosoma andS.trossula are junior synonyms of S.interrupta, and represent different color phasein the course of the sex reversal from female to male.
    Download PDF (2393K)
  • Kiyoshi Maruyama, Kenji Ono
    1974 Volume 21 Issue 2 Pages 108-109
    Published: November 30, 1974
    Released on J-STAGE: June 28, 2010
    JOURNAL FREE ACCESS
    Fishes of the family Melanostomiatidae previously recorded from Japan include seven species in live genera.In 1972, the junior author found a specimen of Melanostomias albibarba Regan and Trewavas in the northern Pacific (38°58.0'-39°7.5'N, 142°12.8'-142°15.5'E).This specimen here reported represents the first record of the species from Japan.A new Japanese name “Shirohige-hoshieso”is proposed.
    Download PDF (1691K)
feedback
Top