• Animal Systematics, Evolution and Diversity
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• v.13 no.1
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• pp.1-8
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• 1997

The first zoeae of Hyastenus elongatus (Ortmann, 1893) were obtained in thelaboratory from hatching. They are described, illustrated in detail and compared with the previously described zoeae of the subfamily pisinae. The zoeae of H. elongatus are similar to, but may be distinguished from those of Hyastenus diacnathus (De Haan, 1839), by the number of setae on the postero-lateral carapace margin and mouthpart appendages, and the length of a dorsal carapace spine. In the mouthpart appendages, the difference in the number of setae on an endopod of the maillule between H. eleongatus and H. diacanthus is doubtful, and it should be necessary ot make a detailed re-description of H. diacanthus.

• Animal cells and systems
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• v.12 no.4
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• pp.279-286
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• 2008

Development and distribution of larval Dungeness crab, Cancer magister Dana, 1852 were investigated in southeastern Alaska from late May to mid-September in 2004. Larvae were collected during daylight hours at three inner and two outer Glacier Bay stations at the two different depths in the water column, above and below the thermocline. Larval density decreased dramatically for three larval stages, zoeae I(ZI), zoeae IV, and zoeae V(ZV), but relatively little for zoeae II and zoeae III. ZI predominated at all stations in late May and were collected until late July. Larval stages progressed seasonally from ZI to ZV and density decreased from ZI through ZV. The densities of each zoeal stage at the inner and outer bay stations and at the shallow and deep depths were similar. The density of each larval stage above(shallow) and below(deep) the thermocline and between inner and outer bay stations were not significantly different. The occurrence of larval Dungeness crab is dramatically later than in other parts of the species range, in that larvae appear in abundance beginning in late May. The pattern of spatial distribution of larval stages for the inland waters of Alaska was also markedly different than the patterns reported for Dungeness crab larvae from other parts of the species range, in that the early and intermediate stages occurred within inland waters; from British Columbia to California these larval stages increase in abundance with distance offshore.

• Animal Systematics, Evolution and Diversity
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• v.18 no.2
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• pp.191-201
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• 2002

The first zoeal stage of Heptacarpus rectirostris (Stimpson, 1860) is re-described and illustrated in detail from laboratory-hatched material. The first zoea of H. rectirostris is more closely related to that of H. futilirostris than to H. camtschaticus, H. pandaloides, and H. geniculatus by having the pterygostomial spine and two anteroventral denticles on the carapace. The former two species, however, can be readily distinguished by the presence (H. futilirostris) or absence (H. rectirostris) of the posterolateral spine on the abdominal somites 4-5. A provisional key to the first zoeas of Heptacarpus for which larval studies are known from Korea and adjacent waters is provided. A list of larval descriptions within the Hippolytidae from Korea and adjacent waters is also included.

• Animal Systematics, Evolution and Diversity
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• v.18 no.2
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• pp.181-189
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• 2002

The first zoeal stage of Palaemon ortmanni (Rathbun, 1902) is re-described and illustrated in detail from laboratory-hatched material. The first zoeas of Palaemon are more closely related to those of Palaemonetes than to Macrobrachium, Leptocarpus, Leander, Leanderites, and Brachycarpus by having the endopod of maxillule with terminal seta and the endopod of maxilla with 2+1 setae. A provisional key to the zoeas between three genera Palaemon, Macrobrachium, and Periclimenes known from Korean waters is included.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.46 no.6
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• pp.801-806
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• 2013

Spiny lebbeid shrimp Lebbeus groenlandicus larvae were reared in the laboratory to estimate the energy budget from the zoeal to the post-larval stage. Energy expended by larvae on growth and respiration was determined from values for feeding, growth, molting, and metabolism. We calculated that 16.22 J were used for growth throughout all larval stages. Energy loss during molting was estimated as 1.03 J, and energy used for respiration was estimated as 1.31 J. Energy taken in by feeding was estimated as 77.16 J, while the sum of energies expended in excretion and egestion was 58.61 J. Larvae were estimated to assimilate 24.6% of ingested food as energy and to use ~85% of the assimilated energy for somatic growth. Gross growth efficiency ($K_1$) and net growth efficiency ($K_2$) were shown to be ~22% and 93%, respectively. Maintenance costs of respiration were estimated as ~9.7% of assimilated energy.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.20 no.6
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• pp.543-560
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• 1987

The complete larval development of the Korean grapsid crab, Acmaeopleura parvula Stimpson, from hatching to first crab was described and illustrated. Larvae were reared in 12 different combinations of temperature and salinity, and passed through five (uncommonly six) zoeal and a megalopal stage. Best survival to first crab stage occurred in $ 20^{\circ}C-31.4\%_{\circ}$. Development to first crab was 22-23 days $(at\;25^{\circ}C)$, 34-37 days $(at\;20^{\circ}C)$ and 50-51 days $(at\;15^{\circ}C)$. Additional sixth zoeae were obtained only at $15^{\circ}C$. Larvae of A. parvula were distinguished from the larvae of other Varuninae in the absence of lateral carapace spines and were morphologically similar to Caetice depressus (De Haan). Other characters of appendages were compared with those of the known larvae of the subfamily Varuninae.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.56 no.2
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• pp.221-227
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• 2023

The vertical distribution of snow crab Chionoecetes spp. larvae in the East Sea were investigated in April 2021 using the Multiple Opening/Closing Net and Environmental Sensing System (MOCNESS). The water temperature ranged from 0.86 to 17.2℃, and salinity from 34.0 to 34.7 psu. Zoea I and II occurred range from 29 to 1,982 inds.10³ m^-3 at 10 stations, and range from 4 to 11 inds.10³ m^-3 at 3 stations, separately. Therefore, Zoea I occurred in wider area and higher density than Zoea II at all stations. In the vertical distribution of larvae, all zoeal stages were mainly distributed in the 30-40 m strata, and the larvae showed nocturnal vertical migration similar to that of most zooplankton. Zoea I appeared in the range from 13.7 to 15.8℃ and occurred at the highest density of 1982 inds.10³ m^-3 at 14℃. And Zoea II appeared range from 13.4 to 14.5℃ and occurred in the highest density of 11 inds.10³ m^-3 at 13.4℃. In conclusion, the early larval stage (zoea I) occurred at a higher range of sea surface temperature than later larval stage (zoea II).

• Korean Journal of Fisheries and Aquatic Sciences
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• v.3 no.3
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• pp.187-198
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• 1970

The author succeeded in rearing the young blue crab from the first stage of zoe ato the true crab shape, and during this time he observed their growth and metamorphosis. The relationships between the number of eggs carried by female crabs (E) and the carapace width (C) and body weight (W) are shown as follows: E= 27.9049C-281.8155, E=0.5682 W-116.4606. There are five zoeal stages and a megalopa in the complete larval development of the blue crab. Water temperature in rearing aquaria ranged from 21.4 to $25.2^{\circ}C$. The duration of each zoeal stage was two days on the average. After the fifth moulting, the zoea becomes megalopa and 5 to 6 days later the megalopa moults and develops into the first stage of adult crab shape. The carapace width of megalopa measured about 1.70 mm and the carapace length, from the tip of the rostrum to the posterior dorsal margin of the carapace, was about 2.78 mm on the average. The carapace width and length of the first crab, 18 days after hatching, measured about 4.48 mm and 2.62 mm respectively. After two days, the first crab moulted and grew into the second crab with about 6.47 mm in carapace width and 4.66 mm in carapace length. The larval rearing in the outdoor tank shelved better results than in the indoor aquarium. The highest mortality occurred when the first stage of zoea moulted into the second stage. Percentage of crabs which survived, from the first crab to the ninth crab stages, was about $55\%$. The relationships between rearing days (D) and the carapace width (C), carapace length (L) and body weight (W) of the crab stages during 40 days of rearing are shown as follows. Carapace width, Indoor: C=1.1250D+1.7227 Outdoor C=1.3465D -0.2449 Carapace length, Indoor: L=0.6654D+1.6712 Outdoor: L=0.7893D+0.6919 Body Weight, Outdoor: $$W=1.15e^{0.12423D}$$ Indoor: $$W=6.759\times10^{-2}D^{1.2598}$$ (9-19 day old crabs) Outdoor: $$W=4.136\times10^{-2}D^{1.6024}$$ (21-40 day old crabs) During the crab stage, the following relationships between the number of moulting times and the carapace width (C), carapace length (L) and body weight (W) were found as follows: $$C=5.2e^{0.28119N}$$ $$L=3.65e^{0.26372N}$$ $$W= 0.14e^{0.7037N}$$ The relationships between the carapace length (L) and the carapace width (C) and body weight (W) of the crab stages are shown as follows: Carapace length, mm Formula 2.62-27.17 L=1.6864C-1.0387 7.47-18.53 $$W=9.367\times10^{-5}C^{3.5567}$$ 22.11-27.17 $$W=3.406\times10^{-5}C{3.8571}$$

• Journal of Aquaculture
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• v.9 no.2
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• pp.179-186
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• 1996

Zoeal stage's larvae of pandalid shrimp Pandalus hypsinotus, is distributed off the East sea and esteemed as a valuable shrimp resource in Korea, were reared in $10^{\circ}C$ temperature-controlled chambers and inverstigated the energy budget. The total energy intake per larva of zoea I to VI stages fed on Artemia nauplii was 140.88 J. The energy loss by respiration, molting, and excretion were 16.22 J, 1.19 J, and 106,40 J, respectively. The amount of energy used by growth was 17.07 J. Pandalid larvae assimilated $24.47\%$ of the ingested food. The gross efficiency ($K_1$) calculated by the equation of (growth+exuviae)/ingestion $rate{\times}100$ was $12.96\%$, and the net growth rate ($K_2$) calculated by the equation of (growth rate + exuviae)/(growth rate+ exuviae+ respiration rate)${\times}100$ was $52.96\%$. The percentage used for somatic growth and maintenance among the assimilated energy were $49.51\%$ and $47.04\%$ respectively.

• 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.