• 한국유기농업학회지
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• 제28권2호
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• pp.251-261
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• 2020

친환경 벼 재배지역 위주로 피해가 점차 확대되는 먹노린재(Scotinophara lurida) 방제기술 개발을 위하여 발생생태 및 온도의존 발육모형을 산출하였다. 2019년도 먹노린재 월동 후 생존율 조사결과 총 224마리 중 167마리가 생존하여 생존율은 72.8%였다. 먹노린재 월동성충은 논에 6월 중하순부터 발생하고, 7월 상순에 산란하고, 8월 중하순에 1세대 성충이 발생한다. 온도의존 발육모형을 구하기 위하여 18, 21, 24, 27, 30℃ 14L:10D 조건의 항온기에서 온도별, 발육단계별 발육기간을 조사하였다. 18, 21, 24, 27, 30℃의 온도조건에서 알에서 성충이 될 때까지의 기간은 각각 119.8, 73.1, 53.5, 39.4, 82.0일로 27℃에서 가장 발육이 잘 되었다. Excell 프로그램을 이용하여 온도와 발육속도와의 관계를 2차 다항식으로 분석하여 회귀곡선을 얻었고 이를 근거로 발육단계별 발육영점온도와 유효적산온도를 산출하였다. 알에서 5령 약충까지 먹노린재 발육영점온도는 17.9℃, 유효적산온도는 380.2DD였다.

• 생명과학회지
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• 제11권5호
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• pp.447-456
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• 2001

임신랫드에서 fluoroquinolone 항균제 DW-116에 의해 유발된 발생독성이 모동물의 사료섭취량 감소에 의한 영양 결핍이 주요 원인인지 아니면 DW-116이 배.태자에 직접적으로 작용하여 유발된것인지를 조사하고자 시험물질을 랫드에 임신 6일에서 16일까지 0 및 500 mg/kg 용량으로 반복 경구투여하였다. 사료제한군은 시험물질 투여군의 모동물의 섭취한 동일한 양의 사료를 제한급여하였다. 모든모동물을 임신 20일째에 제왕절개하였고, 모독성 및 발생독성을 평가하였다. 시험물질 투여군에서는 독성증상과 체중의 감소, 투여 및 투여후 기간의 체중증가 억제, 사료섭취량의 감소를 포함하는 모독성이 부형제대조군및 사료제한군에 비해 현저하게 증가하였다. 또한, 태자사망의 증가, 생존태자의 감소, 태자체중과 태반중량의 감소, 태자기형의 증가 및 골환지연을 포함하는 발생독성도 현저하게 증가하였다. 반면, 사료제한군에서는 모체 및 태자에서 경미한 독성고견만 인정되었고, 태자사망이나 태자기형 등의 심각한 발생독성은 관찰되지 않았다. 결론적으로 시험물질투여군에서 관찰된 발생독성은 사료섭취량의 감소에 의한 모체의 영양결핍에 기인된 것이 아니라 DW-116의 투여에 기인된 직접효과인 것으로 판단된다.

• 한국패류학회지
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• 제20권1호
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• pp.75-84
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• 2004

Reproductive cycle, the condition index, sex ratio of the Pacific oysters, Crassostrea gigas were investigated by histological and morphometric data. The specimens were collected in the two oyster farms of Geoje and Namhae, Gyeongsangnam-do, Korea, from November 1995 to October 1996. Growth of shell length in two regions was similar, but growth of total weight of the oyster in Namhae was faster than that in Geoje oyster farm. The spawning periods in female and male clams were from July to October in Geoje and from June to October in Namhae oyster farm. Ripe oocytes were approximately 50 m in diameter. The reproductive cycle of in females and males in Geoje and Namhae oyster farms can be divided into five successive stages: early developing, late developing, ripe, partially spawned and spent/inactive. Monthly changes in gonad developmental phases showed somewhat different patterns between female and male clams except for the spawning period. On the whole, however, monthly changes in the gonad developmental phases showed a similar pattern in the same sex. The sex ratios of females to males in Geoje and Namhae oyster farms were not significantly different from a 1:1 sex ratio ($x^2$ = 0.55 (p > 0.05) in Geoje and $x^2$ = 0.27 ( p > 0.05) in Namhae). Artificial induction of maturation by heating of adult oysters (two-year-old) was investigated from 17 January to 18 March in 1996. Maturity at the fixed water temperature group of $20^{\circ}C$ was 80%, it showed the highest maturity of experimental groups cultured for five weeks. The survival (%) of Crassostrea gigas in the raised water temperature experimental groups (15, 20, $25^{\circ}C$) were over 98.5%, as similar to the control group (100%). But, the survival of C. gigas in the fixed water temperature experimental groups (15, 20, 25, $30^{\circ}C$) were decreased with the increase of the water temperatures. In the fixed water temperature experimental group of $30^{\circ}C$, the survival was 51.1%. Base on these results, the fixed water temperature of $20^{\circ}C$ was the best condition for artificial induction of sexual maturation.

• 한국응용곤충학회지
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• 제57권4호
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• pp.373-379
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• 2018

뽕나무발효톱밥을 이용한 흰점박이꽃무지의 사육 가능성을 검토하기 위하여 발육 및 산란 특성을 조사하였다. 흰점박이꽃무지 유충의 발육기간은 25, 28, $30^{\circ}C$에서 각각 164.0일, 73.3일, 64.8일로 온도가 높을수록 짧아졌다. 평균 유충 최고 무게는 $25^{\circ}C$에서 2.94 g으로 가장 높았으며 온도가 높아질수록 유충 무게는 감소하는 경향이었다. 우화한 암컷 성충의 평균 무게는 25, 28, $30^{\circ}C$에서 각각 0.94 g, 0.51 g, 0.54 g이었으며 수컷 성충 무게가 암컷보다 무거웠다. 뽕나무톱밥에 밀기울을 10% 또는 30% 첨가하여 발효시킨 것이 흰점박이꽃무지 유충 발육에 양호하였다. 유충 집단 사육시 2.5 g 이상인 유충의 누적비율이 75% 정도인 사육 후 75일부터 유충 판매가 가능하였다. 흰점박이꽃무지의 평균 산란수는 83.2개이었으며, 우화 후 3~8주 사이에 전체 산란수의 73%가 산란되었고, 5주째 산란수가 가장 많았다.

• Asian-Australasian Journal of Animal Sciences
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• 제32권9호
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• pp.1458-1468
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• 2019

Objective: As one of the most important metabolic organs, the liver plays vital roles in modulating the lipid metabolism. This study was to compare miRNA expression profiles of the Large White liver between two different developmental periods and to identify candidate miRNAs for lipid metabolism. Methods: Eight liver samples were collected from White Large of 70-day fetus (P70) and of 70-day piglets (D70) (with 4 biological repeats at each development period) to construct sRNA libraries. Then the eight prepared sRNA libraries were sequenced using Illumina next-generation sequencing technology on HiSeq 2500 platform. Results: As a result, we obtained 346 known and 187 novel miRNAs. Compared with the D70, 55 down- and 61 up-regulated miRNAs were shown to be significantly differentially expressed (DE). Gene ontology and Kyoto encyclopedia of genes and genomes enrichment analysis indicated that these DE miRNAs were mainly involved in growth, development and diverse metabolic processes. They were predicted to regulate lipid metabolism through adipocytokine signaling pathway, mitogen-activated protein kinase, AMP-activated protein kinase, cyclic adenosine monophosphate, phosphatidylinositol 3 kinase/protein kinase B, and Notch signaling pathway. The four most abundantly expressed miRNAs were miR-122, miR-26a and miR-30a-5p (miR-122 only in P70), which play important roles in lipid metabolism. Integration analysis (details of mRNAs sequencing data were shown in another unpublished paper) revealed that many target genes of the DE miRNAs (miR-181b, miR-145-5p, miR-199a-5p, and miR-98) might be critical regulators in lipid metabolic process, including acyl-CoA synthetase long chain family member 4, ATP-binding casette A4, and stearyl-CoA desaturase. Thus, these miRNAs were the promising candidates for lipid metabolism. Conclusion: Our study provides the main differences in the Large White at miRNA level between two different developmental stages. It supplies a valuable database for the further function and mechanism elucidation of miRNAs in porcine liver development and lipid metabolism.

• Reproductive and Developmental Biology
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• 제33권2호
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• pp.99-105
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• 2009

Curcumin is a major active component of the food flovour tumeric. It has been used for the treatment of many diseases such as inflammatory and infectious diseases, cancer and other disease due to its antioxidant properties. Curcumin is a powerful scavenger of many free radicals such as superoxide anion, hydroxyl radical and nitric oxide. The objective of this study was to investigate the antioxidative effects of curcumin against hydrogen peroxide on semen quality during in vitro storage of boar semen. The sperm treated with different concentration of curcumin (1, 5 and 10 ${\mu}M$) in the presence or absence of hydrogen peroxide (250 ${\mu}M\;H_2O_2$) were incubated for 3, 6 and 9 hr at $37^{\circ}C$ and analyzed sperm characteristics such as motility, membrane integrity (MI), lipid peroxidation (LPO), reactive oxygen species (ROS) and DNA fragmentation (DF). The sperm motility and MI in $H_2O_2$ treated group ($47.8%{\pm}6.8$ and $24.8%{\pm}2.2$) were significantly decreased when compare to curcumin treated group ($79.8%{\pm}2.7$ and $34.6%{\pm}1.0$, respectively) irrespective of incubation periods(p<0.05). The LPO of spermatozoal plasma membrane was measured by thiobarbituric acid (TBA) reactions for malondialdehyde (MDA), MDA level in control ($11.6{\pm}0.6\;nmol/L{\times}10^6$) and curcumin groups ($10.7{\pm}0.3\;nmol/L{\times}10^6$) were lower than those of curcumin plus $H_2O_2$ ($17.1{\pm}0.8\;nmol/L{\times}10^6$) or $H_2O_2$ group ($22.5{\pm}1.9\;nmol/L{\times}10^6$) from 3 to 9 hr incubation periods. The DF by sperm chromatin dispersion (SCD) test and ROS production measured by 2',7'-dichlorofluorescein (DCF) fluorescence intensity were no significantly difference through all experimental groups (p>0.05). Correlation among evaluation methods for sperm quality, motility vs MI and DF vs ROS was positively correlated while motility vs DF and ROS vs LPO were negatively correlated in all treatment groups. These results demonstrate that curcumin can effectively improve the sperm quality during in vitro storage of boar semen through its hydrogen peroxide scavenging mechanism as an antioxidant.

• Reproductive and Developmental Biology
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• 제33권4호
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• pp.273-281
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• 2009

Antioxidants partially ameliorated the detrimental effects of reactive oxygen species (ROS) on sperm characteristics during in vitro storage. The objective of the present study was to investigate the single or synergetic antioxidative effect of curcumin and Vit. E on the characteristics of fresh boar sperm during in vitro storage. The sperm viability in curcumin, Vit. E supplementation and curcumin+Vit. $E+H_2O_2$ groups remained over 85.0% in 3 hr incubation period, but in 6 hr incubation period, curcumin+Vit. $E+H_2O_2$ groups was sharply dropped than those of curcumin and Vit. E group. The membrane intergrity in all evaluated groups except for $H_2O_2$ group did not significantly difference in 3 hr incubation period. The viability in curcumin or Vit. E supplementation were significantly increased than in curcumin+$H_2O_2$ and Vit. $E+H_2O_2$ group in 6 hr incubation period. The percentage of mitochondrial activity and acrosome intergrity obtained similar trends within same incubation periods irrespective of treatment. The lipid peroxidation of spermatozoal plasma membrane ranged from $11.6{\sim}17.5\;nM/l{\times}10^6$ and $14.0{\sim}19.0\;nM/l{\times}10^6$ in 3 hr and 6 hr incubation periods. In conclusion, curcumin or Vit. E surpplementation alone or cooperatively improved sperm viability index (motility, membrane intergrity, viability and survival rates) and fertility index (mitochondria activity, acrosome intergrity and lipid peroxidation) of fresh boar sperm, indicating that curcumin and Vit. E have a antioxidative properties through its scavenging activity against hydrogen peroxide.

• 한국패류학회지
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• 제23권1호
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• pp.39-49
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• 2007

우리나라 고성군 송지호의 기수역에서 채집된 2배체 일본재첩 (Corbicula japonica) 과 춘천 의암호 담수에서 채집된 3 배체 재첩 (C. fluminea) 을 대상으로 핵형 및 번식특성의 차이점을 확인하기 위해 조사하였다. 2배체인 일본재첩은 25 개 세포들에서 세포당 38 개의 염색체가 관찰되었다. 이들의 핵형은 상동염색체 2 개가 19 쌍을 이루고 있다. 염색체는 11 쌍의 telocentric과 3 set의 subtelocentric 그리고 3 쌍의 submetacentric 그리고 1 쌍의 metacentric 염색체로 구성되어 있었다. 일본재첩은 난생이며 자웅이체로 내반새와 외반새를 갖는 두 쌍의 아가미를 가지나, 이들은 보육낭으로 기능을 하지는 않는다. 난들과 정자들은 기수역에서 체외수정을 한다. 3배체인 재첩은 세포당 54 개의 염색체가 관찰되었다. 이들의 핵형은 상동염색체 3 개가 18 set를 이루고 있었다. 이들 염색체 18 set는 1 개의 metacentric group과 5 개의 submetacentric group, 그리고 12 개의 subtelo 또는 telocentric group으로 이루어져 있었다. 재첩은 난태생이며 기능적 자웅동체이다. 3배체 조건은 자웅동체성과 밀접한 관련을 가진다. 재첩의 경우는 주로 보육낭으로 기능을 하는 내반새 (inner-demibranch) 를 갖는 2 쌍의 아가미를 가진다. 아가미의 내반새 구조에서는 임란기 중에는 완숙란들이 소모되고, 비임란기 중에는 완숙난들이 생식소의 자웅동체 소낭 내에서 생산되어 주기적 변화가 나타났다. 일본재첩과 재첩의 생식소발달 단계들은 조직학적 관찰에 의해 초기활성기, 후기활성기, 완숙기, 부분산란기, 퇴화 및 비활성기의 5 단계로 나눌 수 있었다.

• 한국응용곤충학회지
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• 제25권4호
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• pp.201-207
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• 1986

침입해충(侵入害蟲)인 온실가루이의 분포현황(分布現況), 온도(溫度)가 발육(發育)에 미치는 영향(影響) 및 주내분포(株內分布)에 관(關)한 조사결과(調査結果)는 다음과 같다. 1. 온실가루이는 영구온실내(永久溫室內)의 철쭉, 란타나, 포인세치아 등(等) 27과(科) 39종(種)의 관상식물(觀賞植物)에서 기생(寄生)하였다. 2. 산란전기간(産卵前期間)은 $25^{\circ}C$에서 1.1일(日), 산란기간(産卵期間)은 28.8일(日), 산란후기간(産卵後期間)은 0.5일(日) 성충수명(成蟲壽命)은 26.8일(日)로 $25^{\circ}C$가 적온(適溫)이었고, 숫컷의 성충수명(成蟲壽命)이 약(約) 6일(日) 짧았다. 3. 일당(日當) 산란수(産卵數)는 $25^{\circ}C$에서 9.8개(個), 총산란수(總産卵數)는 305개(個) 였다. 4. 난기간(卵期間)은 $25^{\circ}C$에서 8.2일(日), 유충기간(幼蟲期間)은 8.3일(日), 용기간은 7.5일(日)이었고, 한세대(世代)를 거치는데는 $22^{\circ}C,\;25^{\circ}C,\;30^{\circ}C$에서 각각(各各) 27.5일(日), 23.8일(日), 18.9일(日)로 온도(溫度)가 증가(增加)할수록 짧아지는 경향(傾向)이였다. 5. 난(卵)에서 유충(幼蟲)까지의 발육영점온도(發育零點溫度)는 $8.8^{\circ}C$였다. 6. 난(卵)에서 성충(成蟲)까지의 성공율(成功率)은 $22^{\circ}C,\;25^{\circ}C,\;30^{\circ}C$에 각각(各各) 70.3%, 58.0%, 66.4%였다. 7. 온실가루이 한세대기간(世代期間)동안의 성충(成蟲)과 난(卵)은 상위엽(上位葉)에 유충(幼蟲)은 중위엽(中位葉)에 용은 하위엽(下位葉)에 집중분포(集中分布)하였다.

• 미생물학회지
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• 제7권1호
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• pp.10-21
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• 1969

The effect of glucose and 2-thiobarbituric acid on the biosynthesis of cell constituents such as protein, carbohydrate, DNA, RNA, phospholipid and PCA-soluble phosphate compounds in Chlorella duing the life cycle was measured, and the changes in the content of these main cellular components of the algal cell were analyzed in connection with the nuclear and cytoplasmic divison. In the normal autotrophic synchronous culture the contents of protein, RNA, and DNA in the cell showed a chracteristic changes according to the progress of cell development, increasing more or less throughout all the life cycle. The synthesis of protein is more prominent in the division period nad that of DNA is more active in the ripening period, while the synthesis of RNA is more rapid in the growing and ripening periods than other developmental stages. The period of division cycle was little affected by glucose in the medium, although the synchrony of the growth and cellular division was disturbed and the n value increased. The cotents of protein, carbohydrate, RNA nad DNA of the cell were increased by the glucose treatment throughout all the life cycle. On the other hand, both of cellular growth and division were retarded severely and the n value was decreased by the 2-thiobarbituric acid treatment throughout all the life cycle. On the other hand, both of cellular growth and division were retarded severely and the n value was decreased by the 2-thiobarbituric acid treatment. The synthesis of protein, carbohydrate, DNA, RNA and phospholipid of the cell was also retarded by 2-thiobarbituric acid. In the autotrophic, mixotrophic and 2-thiobarbituric acid-treated cultures, each having different mode cytoplasmic division, a common general schema occurring in the cell during the life cycle may be drawn as follows. The ratio of RNA to protein attains maximum value in the $L_1$-cell stage prior to the nuclear division and thereafter decreases during the periods of ripening and division. The ratio of PCA-soluble phosphate compounds to protein increased from the begining of the culture to $L_4$-cell stage successively and thereafter decreased gradually during the division period, while the ratio of protein to DNA kept almost constant up to the division period and thereafter increased during the division period. Therefore, it is presumed that the increase in the ratio of RNA to protein is to be an inducer of nuclear division and that the cytoplasmic division is induced by the increase in the ratio of protein to DNA.