• Title/Summary/Keyword: First zoea

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The First Zoeal Stage of Echinoecus nipponicus (Decapoda: Pilumnidae: Eumedoninae) Hatched in the Laboratory

  • Lee, Seok Hyun
    • Animal Systematics, Evolution and Diversity
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    • v.36 no.4
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    • pp.304-308
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    • 2020
  • Ovigerous crab of Echinoecus nipponicus of subfamily Eumedoninae in Pilumnidae was collected from Seogwipo, Jejudo and hatched in the laboratory. The first zoeal stage of E. nipponicus is reported for the first time in the world and its digital image of live zoeas is provided. The first zoea of E. nipponicus has yellowish red chromatophores which occurring behind eyes, on dorsal spine and on anterior margin of telson, reddish brown chromatophores on abdominal somites 2-5 ventrally, dorsal, rostral, and lateral spines shorter than carapace length, three aesthetascs and two setae on the antennule, two medial setae on the antennal exopod, lateral processes on the abdominal somites 2, 3, and two lateral spine and one dorsomedial spine on the telson.

Development and Distribution of the Japanese Mantis Shrimp Oratosquilla oratoria Larvae in the Northwestern Water off Incheon (인천 북서부 해역에서 출현하는 갯가재 유생의 발달과 분포)

  • Yeon, In-Ja;Park, Won-Gyu
    • Journal of Fisheries and Marine Sciences Education
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    • v.23 no.4
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    • pp.763-771
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    • 2011
  • Development and distribution of Japanese mantis shrimp, Oratosquilla oratoria (De Haan) larvae were investigated in the northwestern water off Incheon. O. oratoria larvae were monthly collected at 15 stations from early June to early October in 2007. Bongo net with 330 and 505 um mesh was deployed in a double once with an oblique tow way. Larval densities were relatively higher in southerner stations in July and in northerner stations in August and September. No larvae were discovered in June. Zoea I and II were not captured during the entire sampling period. Zoea III occurred in July for the first time and were found until September. Thereafter, the proportion of later stages increased. The number of zoeal stages decreased during the summer months and no larvae were found in October. Of zoeal stages, zoea IV was the most abundant in number. Zoeal densities were highest in July and August, particularly at the stations near the coast. O. oratoria larvae may be retained and grow within our study sites without advection to growing areas. Non-occurrence of zoea I and II indicate that they were retained near spawning grounds or near parental burrows. Pattern of larval occurrence was coincided with previous researches conducted in conspecific distribution ranges.

Zoeal Stages of Pisidia serratifrons (Crustacea: Decapoda: Porcellanidae) under Laboratory Conditions

  • Kim, Han-Ju;Ko, Hyun-Sook
    • Animal Systematics, Evolution and Diversity
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    • v.27 no.1
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    • pp.53-58
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    • 2011
  • The zoeal stages of Pisidia serratifrons are described and illustrated for the first time and its morphological characteristics are compared with those of three known Pisidia species of the family Porcellanidae. The zoea of P. serratifrons differs from those of other Pisidia (P. brasiliensis, P. dispar, and P. dehaanii), by having 11 spinules on the exopod of the antenna. In order to facilitate the study of plankton-collected material, a provisional key is provided for identification of the Korean porcellanid zoeae.

Zoeal Stages and Megalopa of Hemigrapsus penicillagtus(De Haan, 1835) (Decapoda, BRachyura, Grapsidae) Reared in the Laboratory) (풀게 Hemigrapsus penicillatus(게아목, 바위게과)의 zoea 및 megalopa 유생기)

  • Sang-Gu Hwang;Chang-Hyun Kim
    • Animal Systematics, Evolution and Diversity
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    • v.11 no.3
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    • pp.389-408
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    • 1995
  • The complete larval development of Hemigrapsus penicillatus(De Haan, 1835) from hatching to first crab stage was obtained by culture in the laboratory. Under culture conditions with salinity 33.3% , temperature $25^{\circ}C$, and photophase 14/10 h light/dark, the megalopa and the first crab instar were attained in minimum of 18 and 29 days after hatching respectively. Five zoeal stages and a megalopal stage are described and illustrated in detail. Morphological characters of H. penicillatus larvae were compared with those of other members within the subfamily Varuninae. Morphological differences among H. penicillatus, H. sanguineus and H. sinensis in megalopal stage are tabulated.

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First Zoea of Pagurus joponicus (Crustacea: Decapoda: Anomura: Paguridae) Reared in the Laboratory

  • Ko:yang, Hyun-Sook;Hoi Jeong
    • Animal cells and systems
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    • v.7 no.1
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    • pp.11-14
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    • 2003
  • The first zoeal stage of Pagurus japonicus is described and illustrated. Its morphological characteristics are compared with of other species of the genus Pagurus. The first zoea of P. japonicus was very similar to that of P. similis. The zoeas of the two species could be distinguished from other pagurid zoeas by morphological characteristics of the carapace without posterolateral spine. two setae on the endopod of the antenna, and 3+3 setae on the endopod of the maxilla. They show affinities more to the species of the family Diogenidae than to the species of the genus Pagurus in respect of zoeal morphology.

Studies on the Propagation of the Freshwater Prawn, Macrobrachium nipponense (De Haan) Reared in the Laboratory 2. Life History and Seedling Production (담수산 새우, Macrobrachium nipponense (De Haan)의 증${\cdot}$양식에 관한 생물학적 기초연구 2. 생활사 및 종묘생산에 관한 연구)

  • KWON Chin-Soo;LEE Bok-Kyu
    • Journal of Aquaculture
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    • v.5 no.1
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    • pp.29-67
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    • 1992
  • Life cycle and seed production of the freshwater prawn, Macrobrachium nipponense, were studied and the results are as follows : 1. Larval development : Embryos hatched out as zoea larvae of 2.06 mm in mean body length. The larvae passed through 9 zoea stages in $15{\~}20$ days and then metamorphosed into postlarvae measuring 5.68 mm in mean body length. Each zoea stage can be identified based on the shapes of the first and second antennae, exo- and endopodites of the first and second pereiopods, telson and maxillae. 2. Environmental requirements of zoea larvae : Zoea larvae grew healthy when fed with Artemia nauplii. Metamorphosing rate was $65{\~}72{\%}$ at $26{\~}28\%$ and $7.85{\~}8.28\%_{\circ}Cl.$. The relationship between the zoeal period (Y in days) and water temperature (X in $^{\circ}C$) is expressed as Y=46.0900-0.9673X. Zoeas showed best survival in a water temperature range of $26{\~}32^{\circ}C$ (optimum temperature $28^{\circ}C$), at which the metamorphosing rate into postlarvae was $54{\~}72\%$ The zoeas survived more successfully in chlorinity range of $4.12{\~}14.08{\%_{\circ}}Cl.$, (optimum chlorinity $7.6{\~}11.6\;{\%_{\circ}}Cl.$.), at which the metamorphosing rate was $42{\~}76{\%}$. The whole zoeal stages tended to be longer in proportion as the chlorinity deviated from the optimum range and particularly toward high chlorinity. Zoeas at all stages could not tolerate in the freshwater. 3. Environmental requirements of postlarvae and juveniles : Postlarvae showed normal growth at water temperatures between $24{\~}32^{\circ}C$ (optimun temperature $26{\~}28^{\circ}$. The survival rate up to the juvenile stage was $41{\~}63{\%}$. Water temperatures below $24^{\circ}C$ and above $32^{\circ}$ resulted in lower growth, and postlarvae scarcely grew at below $17^{\circ}C$. Cannibalism tended to occur more frequently under optimum range of temperatures. The range of chlorinity for normal growth of postlarvae and juveniles was from 0.00 (freshwater) to $11.24{\%_{\circ}}Cl.$, at which the survival rate was $32{\~}35\%$. The postlarvae grew more successfully in low chlorinities, and the best growth was found at $0.00\~2.21{\%_{\circ}}Cl.$. The postlarvae and juveniles showed better growth in freshwater but did not survive in normal sea water. 4. Feeding effect of diet on zoea Ilarvae : Zoea larvae were successfully survived and metamorposed into postlarvae when fed commercial artificial plankton, rotifers, and Artemia nauplii in the aquaria. However, the zoea larvae that were fed Artemia nauplii and reared in Chlorella mixed green water showed better results. The rate of metamorphosis was $68\~{\%}75$. The larvae fed cow live powder, egg powder, and Chlorella alone did not survive. 5. Diets of postlarvae, juveniles and adults : Artemia nauplii and/or copepods were good food for postlarvae. Juveniles and adults were successfully fed fish or shellfish flesh, annelids, corn grain, pelleted feed along with viscera of domestic animals or fruits. 6. Growth of postlarvae, juveniles and adults : Under favorable conditions, postlarvae molted every five or six days and attained to the juvenile stage within two months and they reached 1.78 cm in body length and 0.17 g in body weight. The juveniles grew to 3.52 cm in body length and 1.07 g in body weight in about four months. Their sexes became determinable based on the appearance of male's rudimental processes (a secondary sex character) on the endopodites of second pereiopods of males. The males commonly reached sexual maturity in seven months after attaining the postlarvae stage and they grew to 5.65 cm in body length and 3.41 g in body weight. Whereas the females attained sexual maturity within six to seven months, when they measured 4.93 cm in body length and 2.43 g in body weight. Nine or ten months after hatching, the males grew $6.62{\~}7.14$ cm in body length and $6.68{\~}8.36$ g in body weight, while females became $5.58{\~}6.08$ cm and $4.04{\~}5.54$ g. 7. Stocking density : The maximum stocking density in aquaria for successful survival and growth was $60{\~}100$ individuals/$\ell$ for zoeas in 30-days rearing (survival rate to postlarvae, $73{\~}80{\%}$) ; $100{\~}300$ individuals/$m^2$ for postlarvae of 0.57 cm in body length (survival rate for 120 days, $78{\~}85{\%}$) ; $40{\~}60$ individuals/$m^2$ for juveniles of 2.72 cm in body length (survival rate for 120 days, $63{\~}90{\%}$) : $20{\~}40$ individuals/$m^2$ for young prawns of 5.2 cm in body length (survival rate for 120 days, $62\~90{\%}$) ; and $10\~30$ individuals/$m^2$ for adults of 6.1 cm in body length (survival rate for 60 days, $73\~100{\%}$). The stocking density of juveniles, youngs and adults could be increased up to twice by providing shelters.

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The First Zoeal Stages of Parapanope euagora and Halimede fragifer (Decapoda: Pilumnoidea: Galenidae) Hatched in the Laboratory

  • Lee, Seok Hyun;Ko, Hyun Sook
    • Animal Systematics, Evolution and Diversity
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    • v.32 no.2
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    • pp.133-140
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    • 2016
  • The first zoeas of Parapanope euagora and Halimede fragifer hatched in the laboratory from two ovigerous galenid crabs of Pilumnoidea were collected from Jindo Island, Jeolanam-do, southern Korea. Their morphologies are described in P. euagora for the first time in the world and re-described in H. fragifer with the color images of live zoeas. In this study, they show a general morphology of Pilumnoidea by having a long antennal exopod, an endopod of the maxillule with 1, 2+4 setae, an endopod of the maxilla with 3+5 setae, and a fork of the telson with two lateral armatures. However, the first zoea of P. euagora differs from other known zoeas of pilumnoid species including H. fragifer by having a long antennal exopod with a medial seta and spine, not two spines, and a fork of telson with two lateral setae, not a seta and spine. Such characteristics of the antennal exopod and the fork of telson are reported for the first time in the pilumnoid zoeas. A comparison between the first zoeal stage of H. fragifer in this study and that of Terada shows minute differences in the characteristics of the antennule and the fork of telson.

Zoeal Stages of Actaea semblatae (Cruistacea, Decapoda, Xanthidae), with a Key to the Known Xanthid Zoeas of Korea (옴부채게(갑각강, 십각목, 부채게과)의 조에아 유생기 및 한국 부채게과 종의 조에아 유생 검색표)

  • Ko, Hyun-Sook;Yang, Hoi-Jeong;Ban, Kye-Ho
    • Animal Systematics, Evolution and Diversity
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    • v.18 no.1
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    • pp.1-12
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    • 2002
  • Actaea semblatae (Guinot, 1976) has been roared in the laboratory, from hatching to the first young crab stage at $25^{\circ}C$. The two zoeal stages are described and illustrated in detail. The first zoea of A. semblatae in the present study slightly differs from that described by Terada (1987) on the respect of the setal presence on the carapace, the antennule, the coxa of the first maxilliped and the first abdominal somite. Within the family Xanthidae, the zoea of A. semblatae can be clearly distingushed from the other known zoeas by having a seta as an antennal exopod or a vestigial exopod with a sets. A provisional key is provided to aid the identification of the xanthid zoeas in Korea.

ON THE EFFECTS CHLORINITIES UPON GROWTH OF EARLIER LARVAE AND POST-LARVA OF A FRESH WATER PRAWN, MACROBRACHIUM ROSENBERGI(DE MAN) (담수산새우 Macrobrachium rosenbergi (de Man)의 초기유생 및 Post-larva.의 성장에 미치는 염분량에 관하여)

  • KWON Chin Soo;UNO Yutaka;OGASAWARA Yohismitsu
    • Korean Journal of Fisheries and Aquatic Sciences
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    • v.10 no.2
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    • pp.97-114
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    • 1977
  • The fresh water prawn, Macrobrachium rosenbergi(de Man) is a very common species in Indopacific region, which inhaits both fresh and brackish water in low land area, most of rivers and especially aboundant in the lower reaches which are influenced by sea water. It is one of the largest and commercial species of genus Macrobrachium, which is commonly larger than $18\~21cm$ in body length, from the basis of eye-stalked to the distal of telson. As a part of the researches in order to investigate the possibilities on transplantation and propagation of this species, this work dealt with the problems on the effects of chlorinities upon zoeal larvae and post-larvae 1). metamorphosis rate and optimum chlorinity for metamorphosis to post-larve, 2). tolerance and comparative survival rate on various chlorinties, from fresh water to sea water $(19.38\%_{\circ}\;Cl)$, which reared for six days upon each stage of zoeal larvae, 3). accomodation rate on chlonities which reared for twelve days after transmigration into variant chlorinities of the range from $3.68\%_{\circ}$ Cl to $1.53\%_{\circ}$ Cl in the way of rearing of the range from $3.82\%_{\circ}$ Cl to $11.05\%_{\circ}$ upon each stage of zoea, 4). tolerance on both of fresh and sea water upon zoeal larva and post-larva under the condition of $28^{\circ}C{\pm}1$ in temperature and feeding on Artenia salina nauplii, 5). relationship between various chlorinities and grwth of post-larvae under the condition of $28^{\circ}C$ in tmperature and feeding on meat of clam. Thus these investigations were performed in order to grope for a comfortable method on seedmass production. Up to the present, the study on the effects of chlorinity upon earlier zoeal larvae and post-larvae of Macrobrachium species has been scarcely performed by workers with the exception of Lewis(1961) and Ling (1962,, 1967), even so their works were not so detailed. On the other hand, larvae of several species of this genus were reared at the water which mixed sea water so as to carry out complete metamorphosis to post-larva by workers in order to investigate on earlier 1 arval and earlier post-larval development, such as Macrobrachium lamerrei (Rajyalakshmi, 1961), M. rosenbergi and M. nipponense (Uno and Kwoa, 1969; Kwon and Uno, 1969), M. acanthurs (Choudhury, 1970; Dobkin, 1971), M. carcinus(Choudhury, 1970), M. formosense(Shokita, 1970), M. olfersii (Duggei et al., 1975), M. novaehallandiae (Greenwood et al., 1976), M. japonicum (Kwon, 1974) and M. lar (Shokita, personal communication), and there fore it is regarded that chlorinity is, generally, one of absolute factors to rear zoeal larvae of brackish species of Macrobrachium genus. Synthetic results on this work is summarized as the follwings: 1) Zoeal larvae required different chlorinities to grow according to each stage, and generally, it is regarded that optimum range of living and growing is from $7.63\%_{\circ}Cl\to\;7.63\%_{\circ}Cl$, and while differences of metamorphsis rate, from first zoea to post-larva, is rarely found in this range, and however it occurs apparently in both of situation at $7.63\%_{\circ}Cl$ below and $16.63\%_{\circ}Cl$ above and moreover, metamorphosis rate is delayed somewhat in case of lower chlorinity as compared with high chlorinity in these situations. 2) Accomodation in each chlorinity on the range, from fresh water to sea water, is different according to larval stages and while the best of it is, generally, on the range from $14.24\%_{\circ}Cl$ to $8.28\%_{\circ}Cl$ and favorite chlorinity of zoea have a tendency to remove from high chlorinity to lower chlorinity in order to advance larval age throughout all zoeal stages, setting a conversional stage for eighta zoea stage. 3) Optimum chlorinity of living and growth upon postlarvae is on the range of $4.25\%_{\circ}Cl$ below, and in proportion as approach to fresh water, growth rate is increased. 4) Post-large are able to live better in fresh water in comparison with zoeal larvae, which are only able to live within fifteen hours, and by contraries, post-larvae are merely able to live for one day as compared with ?미 larvar, which are able to live for six days more in sea water $19.38\%_{\circ}Cl\;above$. 5) Also, in case of transmigration into higher and lower chlorinities in the way of rearing in the initial chlorinities $ 3.82\%_{\circ}Cl,\;7.14%_{\circ}Cl\;and\;11.05%_{\circ}Cl$, accoodation rate is a follow: accomodation capacity in ease of removing into higher chlorinities from lower chlorinities is increased in proportion as earlier stages, setting a conversional stage for eighth zoea stage, and by contraries, in case of advanced stages from eighth zoea it is incraesed in proportion as approach to post-larva stage in the case of transmigration into lower chlorinity from higher chlorinity. On the other hand, it is interesting that in case of reciprocal transmigration between two different chlorinitiess, each survival rate is different, and in this case, also, its accomodation in each zoea stage has a tendency to vary according to larval stages as described above, setting a conversional stage for eighth zoea stage. 6) It is likely that expension of radish pigments on body surface is directly proportional to chlorinity during the period of zoea rearing, and therefore it seems like all body surfacts of zoea larvae be radish coloured in case of higher chlorinity. 7) By the differences that each zoeal larvae, postlarvae, juvaniles and adult prawn are required different chlorinity for inhabiting in each, it is regarded that this species migrats from up steam to near the estuary of the river which the prawns inhabits commonly in natural field for spawning and growth migration. 8) It had better maintainning chlorinities according to zoeal stage for a comfortable method on seed-mass production that earlier larva stages than eighth zoea are maintained on the range from $8\%_{\circ}Cl\;to\;12\%_{\circ}Cl$ to rear, and later larva stages than eighth zoea, by contraries, are gradually regula ted-to love chlorininity of the range from $7\%_{\circ}Cl\;to\;4\%_{\circ}Cl$ according to advance for post-larva stage.

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Complete Larval Development of Novactaea pulchella (Crustacea: Decapoda: Xanthidae)

  • Ko, Hyun-Sook
    • Animal cells and systems
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    • v.10 no.1
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    • pp.7-14
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    • 2006
  • Novactaea pulchella was reared in the laboratory, from hatching to the megalopal stage at $25^{\circ}C$. The larval stage of it consists of two zoeal and one megalopal stages. The first zoea of the present study differs from that described by Terada (1990) in the setal presence of the carapace, the maxilla and the maxilliped, and the lateral process on the abdominal somite. It is reported for the first time that brachyuran zoeas belonging to a species share two types of lateral processes on the abdominal somites. They are either on the abdominal somites 2 and 3 or on abdominal somites 2 to 5. A provisional key is provided to aid the identification of the actaeine zoeas in Korea and the adjacent waters.