• 한국가축번식학회지
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• 제16권1호
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• pp.63-76
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• 1992

This study was carried out to investigate the appearance time of the second polar body for producing Gynogenesis or Triploid which could be obtained by arresting the second polar body by cold shock, and then blastoderm was used to measure fertility that revealed the nature of oogenesis, the effects of water temperature on fertility, hatchability, abnormality, viability and growth rate, and the water temperature and the breeding methods to prevent early death of larvae in Korean loach(Misgurnus anguillicaudatus) ; the results obtained in this study were summarized as follows. The second polar body was observed ont he surface of plasma disc close to micropyle within 10~40 min after fertilization at 29$^{\circ}C$. Artificial inseminatin had to be done immediately after the egg spawning because the spermatozoa of loach their mobility within 2 minutes when they were exposed to water. The amount of time needed to reach at blastoderm stage was 12 hours if fertilized eggs were incubated at 16$^{\circ}C$, 8 hours at 19$^{\circ}C$, 6 hours at 21$^{\circ}C$, 5 hours at 23$^{\circ}C$, 4 hours at 26$^{\circ}C$ and 3 hours 30 min at 29$^{\circ}C$ showing the shorter time for development of eggs at higher temperature. Fertilization rates in water temperatures of 19$^{\circ}C$, 21$^{\circ}C$, 23$^{\circ}C$, and 26$^{\circ}C$ were higher than those of water temperatures, 16$^{\circ}C$ and 29$^{\circ}C$. Water temperatures at 19$^{\circ}C$, 21$^{\circ}C$, and 23$^{\circ}C$ showed higher hatching rates that those of 16$^{\circ}C$, 26$^{\circ}C$, and 29$^{\circ}C$, while abnormal rates in 16$^{\circ}C$, 19$^{\circ}C$, 21$^{\circ}C$ and 23$^{\circ}C$ were lower than that of 26$^{\circ}C$ and 29$^{\circ}C$. Water temperatures at 16$^{\circ}C$, 19$^{\circ}C$, 21$^{\circ}C$, 23$^{\circ}C$ and 26$^{\circ}C$ respectively, were more different than 29$^{\circ}C$ in survival rates. The embryos were hatched at 72 hours after fertilization in 16$^{\circ}C$ water temperature, 48 hours in 19$^{\circ}C$, 40 hours in 21$^{\circ}C$, 32 hours in 23$^{\circ}C$, 25 hours in 26$^{\circ}C$, and 16 hours in 29$^{\circ}C$. Within three days after hatched out, the larvage grew 3mm in total length, the yolk granules were entirely consumed and the head and the trunk became thicker. Within 45 days after hatched out, the larva grew 25mm at 29$^{\circ}C$, 21mm at 26$^{\circ}C$, 16mm at 23$^{\circ}C$, 15mm at 21$^{\circ}C$, 12mm at 16$^{\circ}C$ in a 30 litreglass aquarium.

• 한국응용곤충학회지
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• 제44권1호
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• pp.61-65
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• 2005

왕귀뚜라미 대량 사육시 요구되는 실내 채란법 개발을 위하여 인공산란매트 선발과 알 저장조건을 조사하였다. 인공산란매트로서 수분 유지능력이 우수한 원예용 오아시스$^{\circledR}$가 천연의 매트인 흙에 비해 산란선호성이 월등히 우수하였다. 한편 인공산란매트로서 원예용 오아시스$^{\circledR}$는 흙에 비해 총산란수 및 부화율이 다소 저조하였으나 산란이 집중적으로 이루어지는 실용 산란기간(성충화 후 50일이내)의 산란수 및 부화율은 오히려 흙에 비해 우수하였다. 알의 저장조건은 산란 후 14일째, $10^{\circ}C$에 40일간 냉장한 구가 부화율 $62.1\%$로 세대단축 등을 고려할 때 단기저장으로 가장 적합한 것으로 판단되었으며, 산란 후 14일째, $7.5^{\circ}C$에 90일 냉장했을 때 부화율 $65.1\%$로 장기저장법으로 가장 적합한 것으로 나타났다.

• 한국패류학회지
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• 제26권4호
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• pp.303-310
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• 2010

개량조개의 인공종묘생산을 위한 유생사육의 최적 사육환경과 먹이생물의 종류에 따른 유생의 성장 및 생존을 조사하였다. 수온에 따른 유생의 성장은 $18^{\circ}C$에서 $33^{\circ}C$까지 수온이 높을수록 빨랐으며, $23^{\circ}C$ 이상에서는 사육 14일째 $230{\mu}m$ 이상 성장하였으나 $18^{\circ}C$에서는 $151.1{\mu}m$로 성장이 부진하였다. 염분별 유생사육 시 염분 30 psu에서 일간 성장은 $11.3{\mu}m$로 가장 빨랐고, 생존율도 65.8%로 가장 높았다. 개량조개 유생은 사육수 1 ml 당 10개체 이하의 밀도에서는 성장과 생존율이 양호하였으나 20개체 이상에서는 다소 성장이 늦어 유생의 사육밀도는 1 ml 당 10개체 이하가 가장 효과적이었다. 개량조개 유생의 빠른 성장과 생존율을 높일 수 있는 유생사육 최적 조건은 수온 $23^{\circ}C$, 염분 30-35 psu, 유생 수용밀도 1-10 개체/ml이었다. 유생사육 시 먹이생물은 미세조류 4종 [Isochrysis galbana, Pavlova lutheri, Isochrysis sp. (green), Chlorella ellipsoidea] 을 혼합 공급한 실험구에서 빠른 성장과 생존율을 높일 수 있으며, 먹이생물을 단일종만을 공급시 I. galbana와 Isochrysis sp. (green) 실험구에서 빠른 성장과 생존율을 높일 수 있었다. 따라서 개량조개 유생의 적정먹이는 I. galbana와 Isochrysis sp. (green)를 포함한 2종 이상을 혼합 공급하는 것이 적합할 것으로 판단된다.

• 한국패류학회지
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• 제27권3호
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• pp.167-173
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• 2011

말백합의 채란 채정 후 경과시간에 따른 수정률과 D형 유생의 발생률은 채란 채정 직후 수정한 것이 가장 높았으며, 1시간 이후부터는 수정률과 발생률이 급격히 감소하였다. 수정란의 적정 발생수온은 $25-27^{\circ}C$였으며, $33^{\circ}C$에서는 정상적으로 발생되지 않았다. 수정란에서 D형 유생까지 발생소요시간은 $20^{\circ}C$에서 37시간 15분, $25^{\circ}C$에서 20시간 50분, $30^{\circ}C$에서 15시간 20분이었다. 초기 발생에 있어 난 발생이 정지하는 생물학적영도는 평균 $12.4^{\circ}C$로 나타났다. 수정란이 D형 유생으로 발생 가능한 염분은 20.0-37.5 psu, 적정염분은 27.5-32.5 psu였다. 발생률이 높은 수정란의 수용밀도는 사육수 1 mL당 40개 이하였다.

• 한국어류학회지
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• 제18권4호
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• pp.339-346
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• 2006

우리나라 고유종인 각시붕어 Rhodeus uyekii의 이용을 위한 연구의 일환으로 동속의 유사종으로 알려진 떡납줄갱이 R. notatus와 상호 교잡을 실시하였다. 이들 두 종은 난의 형태와 크기에 있어 뚜렷한 차이를 보여 잘 구분되었으며, 초기 자어의 난황 형태에 있어서도 각시붕어는 콩깍지모양인 반면 떡납줄갱이는 닻 형이어서 잘 구분되었다. 한편 종간 상호 교잡은 수정율과 부화율에 있어서 정상 교배군과 큰 차이가 없을 정도로 자유로워 UN형이 부화율 71.6%이었으며, NU형이 부화율 97.5%에 달했다. 교잡체의 부화 자어 형태는 UN형에 있어서 극 소수이지만 UU형이 출현하여 주목되었으나 대부분 NN형이 우세한 중간형태이었고, NU형에 있어서는 NN형이 전혀 출현하지 않았고 모두 UU형이 우세한 중간형태로 부계 형질이 우선하는 것으로 사료되었다. 이들 교잡체는 현재 사육중으로 추후 외부형태, 성별 구분, 생식소 기능, 핵형 등을 분석할 예정이다.

• 한국양식학회지
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• 제7권2호
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• pp.89-96
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• 1994

넙치, paralichthys olivaceus 암컷에서 태반성 성선 자극 호르몬 (HCG, human chorionic gonadotropin) 또는 잉어 뇌하수체(CPE, carp pituitary extract)에 의한 산란 유도가 이루어졌다. 대조군은 실험에 사용된 어류중 $30\%$가 산란하였으며, 주사 후 1일에 $0.4\pm0.2\%$의 체중 증가를 보인 반면 HCG 처리군은 $66.7\%$가 산란하였고 주사 후 2일에 최고 $5.6\pm0.4\%$의 체중 증가를 나타내었으며 이후 주사 후 5일까지 체중이 감소하는 경향을 보였다. CPE 처리군은 $44.4\%$의 어류가 산란하였으며 주사 후 3일에$6.4\pm0.5\%$로 체중이 최고로 증가하였으나, 이후 주사 후 5일까지 체중이 감소하는 경향을 보였다. 총 산란량에 있어 대조군은 주사 후 1일과 2일에 각각 85.2g, 41.9g을 보인 반면 HCG 처리군은 처리 후 3일에 200.7g으로 최대 산란 증가를 보였으며, 주사 후 5일까지 총 산란량이 감소하였다. CPE 처리군 역시 주사 후 3일에 269.4g으로 최대 산란을 보인 이후 주사후 5일까지 산란량이 감소하는 경향을 보였다. 호르몬 주사 후 2일, 3일에서 대조군의 부상율과 부화율은 각각 $35\%,\;13\%$ 및 $33\%,\; 20\%$를 나타내었다. HCG 처리군은 주사 후 1일에서 4일까지 부상율 $37\~88\%$, 부화율 $18\~61\%$를 나타내었으며, CPE 처리군은 주사 후 2일에서 4일까지 부상율 $36\~93\%$, 부화율 $35\~76\%$를 나타내었다. 호르몬 처리시의 체중 증가와 부상율, 부화율을 고려하면 HCG는 처리 후 2일 혹은 3일에 CPE는 처리 후 3일 혹은 4일에 최상의 난질 획득이 가능하리라 사료된다.

• Asian-Australasian Journal of Animal Sciences
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• 제14권2호
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• pp.174-183
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• 2001

During the rapid phase of gonadal development of the freshwater teleost, the catfish (Silurus asotus), the influence of hCG upon the inducement of final oocyte maturation and spawning was investigated electrophoretically and ultrastructurally. The electrophoretic patterns obtained were different in the presence and absence of some of the major or minor zones, because of the hormone level in catfish. The vitellogenin of hormone-treated fish was stained more intensively than that of sham-treated fish. These proteins showed some minor or main bands of egg extracts which migrated at positions corresponding to molecular weights of approximately 90,000. However, the thickness of electrophoretic band in molecular weight for hCG-treated fish was slightly lower than that for saline control. It seemed the plasma protein with molecular weight of approximately 45,000 in hCG-treated fish disappeared. In contrast to the control fish, the ovaries in the catfish treated with hCG shows a marked ultrastructural change under the electron microscope. No dilated profiles were seen in the granulosa cells of the mature oocyte before ovulation. After germinal vesicle breakdown (GVBD), the zona radiata interna (ZRI) becomes more compact, and there is a loss of all the processes from the pore canals. There is a wide space between the vitelline membrane and zona radiata. Also, during final maturation, the microvillar processes from the oocyte are seen no longer to penetrate deeply into the extracellular spaces of the overlying granulosa cells, and the reticulate patterns of the zona radiata interna becomes occluded, giving the zona radiata a more solid appearance. It has been possible to initiate 100% oocyte maturation in yolk granules and follicles in vivo by treatment with hCG and a high water temperature ($27^{\circ}C$). In hCG-treated fish, the percentages of successful artificial fertilization and hatching were maximal at 15 h after a single injection. It seems clear that a long acting preparation containing hCG can be successfully used in prespawning fish to advance the final events of gonadal maturation and initiate spawning. Further studies are necessary to evaluate the potential of hCG to either stimulate or inhibit the reproductive development of fish at other stages of the seasonal reproductive cycle.

• 한국양식학회지
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• 제19권3호
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• pp.166-172
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• 2006

동일 종내 미꾸라지(Misgurnus mizolepis) 웅성발생성 인공처녀생식(intraspecific androgenesis)기술을 개발하기 위해 미꾸라지 난 유전물질의 불활성화와 이에 따른 웅성발생성 반수체 유도 조건을 최적화하였다. 다양한 자외선(UV)농도$(0\sim25,650ergs/mm^2)$를 이용하여 미꾸라지 난의 유전학적 불활성화를 시도하였으며 수정률, 부화율 및 반수체 출현율을 평가한 결과 10,800 ergs의 농도에서 가장 우수한 반수체 유도 효율을 보였으며 최초 처리 난 중 50%이상의 웅성발생성 반수체 수율을 확보할 수 있었다. 웅성발생성 개체는 전형적인 haploid syndrome의 특징을 나타내었고 flow cytometry분석 결과 정확히 미꾸라지 반수체(1.4 pg/cell)의 DNA함량을 보유하는 것으로 나타났다. 인위적으로 삽입된 형질전환 유전자 표지를 이용하여 부계 특이적인 인공처녀생식 여부를 확인하였으나 일부 반수체자어들에서$(8\sim11%)$ 모계 유전물질의 잔류가 검출되었다.

• 한국동물학회지
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• 제8권2호
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• pp.89-127
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• 1965

1. This report is on the outcome of observation made up the breeding process of Narcissus flycatcher, Muscicapa narcissina zanthopygia, using 15 ness-boxes at Seoul and Kwang Nung Experimental forest in 1964, and the relevant feeding habit was studied by the collar method of wrapping the necks of thenestlings for 50-60 minutes or more in some cases from 1963 to 1964. 2. The Narcissus flycatcheris a common summer resident throughout Korea arriving at the end of April. The earliest data of arrival of this species in Seoul, is April 26, 1964. They migrate southward from the later part of September to early part of October. 3. In a week after their arrival , they start to build nest after a brief courtship. Male and female prepare their nest ina nestboxes in 4 or 5 days. Nests are usually found in the moss, which provide definite frame-work. The inner side of the nest is usually composed of roots of Gramineae or leaves of pine, oak or other broad leave tree. 4. The laying period is generally from the later part of April to the middle of June : and the number of eggs laid is from 3 to 8 , therefore 5 in average : eggs are pink with traces of milky yellow blending of light auburn and orange red spots and chicken-egg-like in shape. 5.The incubation takes place for 7-12 days from the middle part of May to the middle of June, in the order of male and female . The hatching rate tends to increase in proportion to clutch size. 6. The feeding period usually lasts 15 days in average from the early part of June to the middle of July and the feeding urge tends to increase in proportion to brood size. 7. The animals invading into their nest-boxes are red ants, chipmunks, bees , barkbeetles and philippine red-tailed shirkes, etc. 8. On the basis of analysis covering 714 birds in 31 nests, the food they consumed during the nesting period of nestlings were mostly of animal matters composing of : insect larvae form-39. 88% insect adult form 36.26%, insect pupae-0.19%, spider-17.75% and other animal matters 5.92% , Besides a small amount of plant pieces were found . As to the insect larvae, Lepidoptera was the largest in the content followed by Hymenoptera , Orthoptera and Coleoptera. As to the insect adult, Diptera was the largest in the content followed by Coleoptera, and Hymenoptera. In view of forest protection, noxious insect was of 69.38%, useful insect 4.39%, and spider 17.75%. 9. The rich assortment of its food, the ability of acquiring various insect (adults as well as larvae), its destruction of great numbers of harmful insects , and its quick assimilation artificial nesting with the nest-boxes of 2.5-3cm entrance hole employed, allow us to conclude that the flycatcher may be successfully employed in the elimination of fores pests. The above results are only that part obtained near Seoul in the middle of Korea, however, if we would extend the scheme to other broad areas using similar techniques, the nest-boxes could not only be well used by the birds, but also it would help to prevent the increase of harmful. insects.

• 대한수의학회지
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• 제38권1호
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• pp.107-117
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• 1998

The cultivation for development of Ascaris suum from the second-stage larvae($L_2$) embryonated egg and the third-stage of rat-derived larvae($L_3$) recovered from lung of rats were performed to use the screening test of anthelmintics in vitro. The preparations of larvae for cultivation were that the artificially-hatched $L_2$ incubated the embryonated eggs of Ascaris suum in 0.1% formalin solution at $25^{\circ}C$ for 28 days and the rat-derived larvae($L_3$) recovered from the lung of rat infected with the embryonated eggs of Ascaris suum on 7 days after infection(DAI). The cultivation for development of Ascaris suum from the embryonated eggs($L_2$) and the rat-derived larvae($L_3$) for 14 days in RPMI medium 1640(with 5% bovine calf serum) were as follows : 1. The sizes of the liberated larvae($L_2$) which were artificially hatched from embryonated eggs with glass beads(diameter 5mm) were $190{\sim}250{\mu}m$ on 1 days in culture(DIC). The second-stage larvae were molted into third-stage larvae(early $L_3$; $250{\sim}300{\mu}m$) and the features of these larvae were first observed such as cephalic cuticle, esophageal lumen and anus etc. on 5 DIC and the sizes of late third-stage larvae were $250{\sim}450{\mu}m$ on 10 DIC. The sizes of early fourth-stage larvae($L_4$) were $500{\sim}700{\mu}m$ and the features of these larvae were more pronounced in internal organs on 15 DIC. 2. The sizes of third-stage larvae($L_3$) recovered from the lung of rats were $1,340{\sim}1,370{\mu}m$ and the feartures of cephalic cuticle, esophageal lumen, intestine, rectum, anus were visualized by inverted microscope on 1 DIC. The fourth-stage larva($L_4$) completed by third ecdysis were recognizable and sizes of early fourth-stage larvae were developed as $1,400{\sim}2,200{\mu}m$ on 5 DIC. The sizes of middle fourth-stage of larva were $1,900{\sim}2,300{\mu}m$ and the thickened epithelial rectum was observed on 10 DIC. The rectum and anus of late fourth-stage larva($L_4$ $2,500{\sim}3,200{\mu}m$) had developed completely in RPMI medium 1640 on 15 DIC.