• Title/Summary/Keyword: Hatching Rate

Search Result 465, Processing Time 0.027 seconds

Hatching Rate and Larval Viability of Cultured Marine Fish Exposed to Water-soluble Fraction of Kuwait Crude Oil during Egg Development (난발생중 원유의 수용성 성분에 노출된 해산 양식어류 수정란의 부화율 및 자어의 생존능력)

  • 이갑현;장영진;강덕영
    • Journal of Aquaculture
    • /
    • v.12 no.2
    • /
    • pp.115-122
    • /
    • 1999
  • Exposure experiments during the egg development were conducted to assess the influences of 5 different concentrations (0, 25, 50, 75 and 100%) of water-soluble fraction (WSF) of Kuwait crude oil on the eggs and larvae of black seabream (Acanthopagrus schlegeli), red seabream (Pagrus major) and olive flounder (Paralichthys olivaceus). All experiments were triplicated. Hatching time and hatching rate were examined on the eggs. The median lethal time ($LT_{50}$), morphological abnormality and swimming activity (swimming frequency and speed) of larvae were also investigated. The time and rate of egg hatching were not significantly influenced by WSF on the eggs of the fishes. The larvae exposed to WSF during the egg development were also not significantly influenced on the $LT_{50}$ and swimming activity. But the higher morphological abnormalities of notochord were observed from the larvae in 100% WSF exposure.

  • PDF

Biochemical Overripeness Characterization of Artificially Maturated Japanese Eel Anguilla japonica Egg (인위적으로 성숙시킨 뱀장어 Anguilla japonica 성숙란의 생화학적 과숙 특징)

  • Kwon, O-Nam;Adachi, Shinji
    • Journal of Aquaculture
    • /
    • v.21 no.3
    • /
    • pp.176-180
    • /
    • 2008
  • This study clarified biochemical overripeness characterization of ovulated eggs of Anguilla japonica and suggested a method maintained overripeness after ovulation for high hatching rates. In maturated Japanese eel eggs, the relationships between fertilization rate and hatching rate, and fertilization and survival rates were measured. DNA contents showed the significantly low 0.653 pg/ug protein in 20% downward hatching rate trial with decrease of hatching rate(P<0.05), whereas RNA/DNA ratio showed the significantly high 1.058 in 20% downward hatching rate trial(P<0.05). And activities of total alkaline protease and ACPase according to the hatching rate groups did not show the significant difference(P>0.05). The protein contents were assayed the significantly high 186.16 ug/mg protein in 20% downward hatching rate trial(P<0.05). However, the overripened eggs had lowed hatching rate, because of stimulate the overripening of normal maturated eggs due to the continuous supplement of protein (vitellogenin). We suggested that need to reduce supplement speed or interception of vitellogenin produced in live for prevent overripeness of maturated eggs after ovulation

Effects of Incubation Method and Transfer Timing on the Hatching Rate of Fertilized Eggs of the River Puffer Takifugu obscurus (황복(Takifugu obscurus) 수정란의 부화방법 및 수송 시기에 따른 부화율 조사)

  • Yoo, Gwangyeol;Hur, Junwook
    • Korean Journal of Fisheries and Aquatic Sciences
    • /
    • v.54 no.1
    • /
    • pp.124-128
    • /
    • 2021
  • This study was conducted to evaluate the effects of incubation methods and transfer timings on the hatching rate of fertilized eggs of the river puffer Takifugu obscurus. Four incubation methods were tested, a) control (fertilized eggs attached to the glass plate), b) bottom (fertilized eggs spread on the bottom of the tank without any treatment), c) S-bottom (removing the stickiness of the fertilized eggs, and then spreading the eggs on the bottom of the tank), and d) incubator (removing the stickiness of the fertilized eggs, and then incubating the eggs in an incubator). Additionally, four transfer timings were tested: a) control (no transfer from the incubation tank), b) zygote (fertilized eggs transferred at the zygote stage), c) segmentation (fertilized eggs transferred at the segmentation stage), and d) pharygula (fertilized eggs transferred at the pharygula state). The results showed that the hatching rate of incubator was significantly higher than those of control, bottom, and glass (P<0.05). The results also showed that the hatching rates of control and pharygula were significantly higher than those of zygote and segmentation (P<0.05).

Effect of Making a Hole in Zona Pellucida by Laser on Hatching of Frozen-thawed ICR Mouse Embryos (레이저를 통한 투명대내의 천공이 동결융해 ICR 마우스 수정란의 부화에 미치는 영향)

  • Yong, Hwan-Yul
    • Journal of Embryo Transfer
    • /
    • v.23 no.1
    • /
    • pp.1-4
    • /
    • 2008
  • This study was performed to investigate the effect of laser-assisted hole in the zona pellucida (ZP) of frozen-thawed ICR mouse embryos on the process of hatching that is critical for expanded blastocysts to implant into endometrium, Vitrification medium, composed of ethylene glycol and sucrose supplemented with 7.5% (w/v) PVP, was used to freeze $2{\sim}4$ cell stage embryos recovered from oviducts of superovulated and mated female mice before storing them in $LN_2$. Right after thawing them, a laser beam was shot to make a hole in ZP followed by culturing in KSOM for $96{\sim}120\;hr$ and examining development to blastocyst and hatching every 12 hr. Laser-treated embryos showed significantly higher hatching rate compared to control (92.9% vs. 22.1%, p<0.05). From around Day 4, blastocysts developed from laser-treated embryos started hatching while the blastocysts of control group failed to hatch showing a lot of shrinkage. This study shows that a laser-assisted hole in ZP improves the hatching rate of blastocysts developed from frozen-thawed, in vitro cultured ICR mouse embryos.

The Effect of Incubation Temperature at Egg Hatching of the Boreal Digging Frog, Kaloula borealis (부화 온도가 맹꽁이(Kaloula borealis)알의 부화에 미치는 영향)

  • Jeong-Rae Rho
    • Korean Journal of Environment and Ecology
    • /
    • v.38 no.2
    • /
    • pp.143-147
    • /
    • 2024
  • This study aimed to determine the egg-hatching period of boreal digging frogs, Kaloula borealis, and investigate whether the incubation temperature affects the hatching period. In this study, the egg hatching was recorded based on the appearance of the tadpole. The results of this study showed that all the eggs hatched within 48 hours after spawning, with 28.1% (±10.8, n=52) hatching within 24 hours and 99.9% (±0.23, n=49) within 48 hours after spawning. The mean hatching rate of tadpoles showed significant differences depending on the difference in water temperature. The mean hatching rate between 15 and 24 hours after spawning was higher at a water temperature of 21.1 (±0.2) ℃ than at 24.1 (±0.2) ℃. The results suggest rapid hatching occurs at relatively low water temperatures because the spawning habits that spawn eggs in temporary ponds or puddles in the rainy season require rapid hatching before the puddles dry out. The results of this study are helpful for understanding the most suitable temperature conditions for the incubation of eggs of the endangered species, boreal digging frog.

G Protein Mediated Hatching Regulation in the Mouse Embryo

  • Cheon, Yong-Pil
    • Development and Reproduction
    • /
    • v.16 no.1
    • /
    • pp.69-75
    • /
    • 2012
  • Hatching occurred in the time dependent manners and strictly controlled. Although, the hatching processes are under the control of muti-embryotrophic factors and the expressed G proteins of cell generate integrated activation, the knowledge which GPCRs are expressed during hatching stage embryos are very limited. In the present study, which G proteins are involved was examined during blastocyst development to the hatching stage. The early-, expanded-, and lobe-stage blastocysts were treated with various $G_{\alpha}$ activators and H series inhibitors, and examined developmental patterns. Pertusis toxin (PTX) improved the hatching rate of the early-stage blastocyst and lobe-formed embryos. Cholera toxin (CTX) suppressed the hatching of the early-stage blastocyst and expanded embryos. The effects of toxins on hatching and embryo development were changed by the H7 and H8. These results mean that PTX mediated GPCRs activation is signaling generator in the nick or pore formation in the ZP. In addition, PTX mediated GPCR activation induces the locomotion of trophectoderm for the escaping. CTX mediate GPCRs activation is the cause of suppression of hatching processes. Based on these data, it is suggested that various GPCRs are expressed in the periimplantation stage embryos and the integration of the multiple signals decoding of various signals in a spatial and temporal manner regulate the hatching process.

Production of Healthy Shrimp(Penaeus chinensis, Penaeus japonicus) Seedling Free from White Spot Baculovirus(WSBV) (White Spot Baculovirus(WSBV) 미감염 새우(Penaeus chinensis, Penaeus japonicus) 종묘 생산)

  • Heo, Moon-Soo;Sohn, Sang-Gyu;Kim, Jong-Sik
    • Journal of fish pathology
    • /
    • v.14 no.1
    • /
    • pp.11-15
    • /
    • 2001
  • For the production of healthy shrimp(Penaeus chinensis, Penaeus japonicus) seedlings free from the white spot baculovirus(WSBV), we tried to disinfect shrimp eggs with iodine. A relative hatching rate of over 50% has resulted from the treatments of fertilized eggs of fresh shrimps(P. chinensis) with an effective povidon-iodine concentration of 20-200 ppm for 30 seconds and 60 seconds, respectively. The 60 sec treatment group with a 20 ppm effective povidon-iodine concentration showed nearly a 50% relative hatching rate. The over 50 ppm treatment group, however, did not result in hatching show a relative hatching rate. These hatching rates were similar to those in the fertilized eggs of kuruma prawns treated with povidon-iodine solutions. In case of washing fertilized eggs with UV-irradiated seawater 33.3% relative hatching rate in fresh shrimps was much lower than 55.2% in kuruma shrimps. Treatment fertilized eggs of 2 species of shrimp with 200 ppm iodine for 30 sec did not affect the survival rate of the larvae until the early stage of the post larvae even though the hatching rates were low. In order to produce healthy shrimp seedlings non-infected by WSBV, the shrimp eggs should be washed with UV-irradated seawater and sterilized with a low povidon-iodine concentration for a short time.

  • PDF

Effect of Temperature on Hatching Rate of Nannophya pygmaea eggs (Odonata: Libellulidae) (꼬마잠자리(Nannophya pygmaea Rambur: Libellulidae, Odonata) 알의 부화에 미치는 온도의 영향)

  • Kim, Dong-Gun;Yum, Jin-Whoa;Yoon, Tae-Joong;Bae, Yeon-Jae
    • Korean journal of applied entomology
    • /
    • v.45 no.3 s.144
    • /
    • pp.381-383
    • /
    • 2006
  • The hatching rate of the eggs of Nannophya pygmaea Rambur, an endangered dragonfly species in Korea, was experimented in different temperature conditions ($10,\;15,\;20,\;25,\;and\;30^{\circ}C$) in laboratory. N. pygmaea eggs were collected from female adults inhabited a small wetland in Mungyong-si, Kyeongsangbuk-do, Korea, in July 2006. The hatching rate was evaluated from the number of hatched nymphs for the period of 100 days. As a result, the hatching rates were 83, 89, and 76% at $20,\;25,\;and\;30^{\circ}C$, respectively; however, eggs were not hatched at $10^{\circ}C\;and\;15^{\circ}C$ during the experiment period. The derived thermal threshold for egg hatching was $14.3^{\circ}C$, which is relatively higher than the values of other temperate dragonflies.

Effects of various freezing containers for vitrification freezing on mouse oogenesis

  • Kim, Ji Chul;Kim, Jae Myeoung;Seo, Byoung Boo
    • Journal of Animal Science and Technology
    • /
    • v.58 no.3
    • /
    • pp.13.1-13.7
    • /
    • 2016
  • Background: In the present study, various freezing containers were tested for mouse embryos of respective developmental stages; embryos were vitrified and then their survival rate and developmental rate were monitored. Mouse two cell, 8 cell, and blastula stage embryos underwent vitrification freezing-thawing and then their recovery rate, survival rate, development rate, and hatching rate were investigated. Methods: EM-grid, OPS, and cryo-loop were utilized for vitrification freezing-thawing of mouse embryos. Results: It was found that recovery rate and survival rate were higher in the group of cryo-loop compared to those of EM-grid (p < 0.05). Embryonic development rate, two cell embryos to blastocyst, as well as hatching rate were higher in the control group compared to the EM-grid group and OPS group (p < 0.05), yet no difference was noted between the control group and cryo-loop group. Development rate and hatching rate of eight cell morulae and blastocysts were all lower in the treatment groups than the control group whilst hatching rate of blastocysts was higher in the control group compared to the groups of EM-grid and OPS (p < 0.05); although the cryo-loop group was shown to be slightly higher than other groups, it was not statistically significant. Conclusions: In the study, we investigate effects of freezing containers on vitrified embryos of respective developmental stages; it was demonstrated that higher developmental rate was shown in more progressed (or developed) embryos with more blastomeres. There was however, no difference in embryonic development rate was shown amongst containers. Taken together, further additional studies are warranted with regards to 1) manipulation techniques of embryos for various vitrification freezing containers and 2) preventive measures against contamination via liquid nitrogen.

Reproductive Strategies in Great Tits

  • Yoo, Jeong-chil
    • Proceedings of the Zoological Society Korea Conference
    • /
    • 1995.10a
    • /
    • pp.68-73
    • /
    • 1995
  • Most female Great Tits lay one egg each day until the clutch is complete. However, some exceptions are found. “Pause day/s” most frequently occur after the 1st egg is laid. In general, egg-size increase with laying sequence, but there is year-to-year variation. The relationship between egg size and laying sequence is found more significantly in relatively larger clutches than in smaller ones. Great Tits tend to advance the hatching of their chicks by starting to incubate earlier in relation to clutch completion as the breeding season progresses. hatching asynchrony affects chick´s growth rate, but when the effect of laying date on hatching asynchrony is controlled, the effect of hatching asynchrony on growth rate is not found. These findings support the ´hurry-up´ hypothesis.

  • PDF