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"The effect of Dimethyl Formamide (DMF) as a cryoprotectant on spermatozoa quality of carp fish Cyprinus carpio race Majalaya 24 hours post-cryopreservation was studied. This study was conducted in the Environmental Engineering Laboratory. Puspiptek. Serpong. Sperm was collected by the hand stripping method and were immediately diluted with extender [6J and cryoprotectant (DMF). The final concentrations of DMF were 0. 3.75. 7.5. and ! 1.25%. respectively. Sperm were frozen in liquid nitrogen for 24 hours. All sperm were re-examined after thawing for motility. viability, and abnormality. The highest percentage of the molility and the viability of preserved sperm was showed or the DMF 7.5%. On the oiher hand the lowest percentage of the abnormality of preserved sperm was demonstrated by the DMF 7.5%. also. Accordingly. DMF 7.5% is the optimum levels that could preserved spermatozoa still in a good quality 24 hours posl-cryopreservation."

"ABSTRAKPenelitian kriopreservasi spermatozoa ikan lukas memiliki tujuan mengetahui pengaruhberbagai konsentrasi susu skim (0%, 5%, 10%, 15%, 20%, 25%) terbaik terhadapmotilitas, viabilitas dan abnormalitas serta kemampuan fertilisasi spermatozoa ikanlukas pascakriopreservasi. Larutan pengencer yang digunakan dalam penelitian adalahlarutan Fish Ringer, dengan rasio pengenceran yang digunakan adalah 1:9.Kriopreservasi dilakukan pada deep freezer dengan suhu -34°C, dengan lamapenyimpanan selama 48 jam. Spermatozoa hasil kriopreservasi selama 48 jamdigunakan untuk membuahi sel telur ikan lukas. Hasil fertilisasi digunakan untukmengukur parameter kualitas spermatozoa yang baik. Berdasarkan hasil uji ANAVAsatu arah menunjukkan pemberian berbagai konsentrasi susu skim memiliki nilai rataratapersentase motilitas, viabilitas, dan abnormalitas spermatozoa ikan lukas 48 jampascakriopreservasi yang berbeda nyata (P<0,05). Hasil terbaik ditunjukkan padakonsentrasi susu skim 20% dengan nilai persentase motilitas, viabilitas danabnormalitas secara berurutan sebesar 81,70 ± 0,70%; 80,37 ± 2,72%; dan 25,87 ±1,7%. Hasil analisis pada fertilisasi pascakriopreservasi menyatakan bahwa nilai rataratapersentase fertilisasi tidak berbeda nyata antar perlakuan, namun pada konsentrasisusu skim 20% kemampuan fertilisasi mampu dipertahankan dengan baik terlihatdengan nilai rata-rata fertilisasi tertinggi yaitu 65 ± 6,45%.

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ABSTRACTThe objective of this study was to discover the effect of skim milk from variousconcentration (0%, 5%, 10%, 15%, 20%, and 25%) which give the best effect towardsmotility, viability, abnormality and fertilization capability of Puntiusbramoides spermatozoa two days after freezing. We used Fish Ringer to dilute thespermatozoa at 1:9 ratio. Based on the ANOVA analysis, the treatment groups showedsignificant difference in average motility, viability and spermatozoa abnormalitypercentage with the control (P<0.05). Tukey test showed best result are obtained from20% skim milk with average motility (81.70 ± 0.70%), sperm viability (80.37 ± 2.72%),and sperm abrnormality (25.87 ± 1.7%). The analysis from postcryopreservationfertilization showed no significant difference (P>0.05) in average motility percentagebetween treatment groups and control. However, the highest concentration percentageof fertility (65 ± 6,45%) was shown by the combination of 20% skim milk and 10%methanol."

"Penelitian pengaruh pemberian berbagai konsentrasi kuning telur ayam kampung terhadap kualitas spermatozoa ikan koi Cyprinus carpio, Linnaeus 1758 48 jam pascakriopreservasi dilakukan untuk mengetahui konsentrasi optimum kuning telur ayam kampung yang dapat digunakan untuk menjaga kualitas spermatozoa ikan koi. Semen ikan koi diperoleh dengan cara stripping pada bagian urogenital ikan koi. Evaluasi semen ikan koi dilakukan secara makroskopis volume, pH, dan warna semen dan mikroskopis persentase motilitas, viabilitas, dan abnormalitas. Penelitian menggunakan larutan pengencer metanol 10 dan berbagai konsentrasi kuning telur ayam kampung dengan perbandingan semen dan pengencer 1:4. Perlakuan yang diberikan yaitu kuning telur ayam kampung dengan konsentrasi 0 kontrol, 5, 10, 15, 20, dan 25. Pembekuan dilakukan pada suhu -34 oC selama 48 jam. Data yang diperoleh menunjukkan distribusi normal dan bervariasi homogen setelah dilakukan uji normalitas Shapiro-Wilk dan uji homogenitas Levene. Hasil uji Analisis Variansi ANAVA satu arah menunjukkan pengaruh perlakuan kuning telur ayam kampung.

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Research about various effect of free range chicken egg yolk concentration to spermatozoa quality of Koi Fish Cyprinus carpio, Linnaeus 1758 48 hours post cryopreservation was done to know optimum concentration of free range chicken egg yolk that can still keep the quality of koi fish spermatozoa. Milt sperm koi fish was collected by stripping at urogenital area of the fish. Koi fish sperm evaluation was done macroscopically volume, pH, milt color and microscopically percentage of motility, viability, and abnormality of spermatozoa.

The research was using dilution solution methanol 10 and various concentrations of free range chicken egg yolk with ratio 1 4. The given concentration of free range chicken egg yolk was 0 control, 5, 10, 15, 20, and 25. Freezing was done at 34 oC for 48 hours. The data obtained showed normal and homogenous after processed with the Shapiro Wilk normality test and Levene homogenity test. The one factor ANOVA showed that various concentration of free range chicken egg yolk had effect."

"ABSTRAKKriopreservasi merupakan metode penyimpanan materi genetik pada suhu yang rendah dalam jangka waktu yang lama. Manfaat kriopreservasi salah satunya untuk mengatasi masalah penurunan populasi. Ikan kancra merupakan salah satu spesies dari famili Cyprinidae yang populasinya semakin menurun sehigga diperlukan upaya pelestarian. Faktor yang mempengaruhi keberhasilan kriopreservasi salah satunya adalah krioprotektan. Krioprotektan alami digunakan karena memiliki toksisitas yang lebih rendah dibanding krioprotektan dari bahan kimia. Kuning telur merupakan krioprotektan alami yang dapat menjaga sel selama proses kriopreservasi. Tujuan dari penelitian yaitu mengevaluasi efek kuning telur ayam kampung sebagai krioprotektan alami terhadap motilitas, viabilitas, abnormalitas dan fertilisasi spermatozoa 48 jam pascakriopreservasi. Konsentrasi kuning telur ayam kampung yang digunakan yaitu: 0%, 5%, 10%, 15%, 20% dan 25%. Rasio yang digunakan untuk pengenceran sperma yaitu 1:10. Analisis data menggunakan uji ANAVA kemudian dilanjutkan dengan uji Tukey. Berdasarkan hasil uji ANAVA satu arah diketahui bahwa krioprotektan kuning telur ayam kampung yang dikombinasikan dengan metanol 10% memberikan pengaruh (P<0,05) terhadap motilitas, viabilitas, abnormalitas dan fertilitas spermatozoa pascakriopreservasi. Konsentrasi kuning telur 5% merupakan konsentrasi optimum yang dapat mempertahankan persentase motilitas, viabilitas dan fertilitas tertinggi masing-masing 84,06 ± 1,67%, 82,13 ± 1,75% dan  92,96 ± 1,94% serta nilai persentase abnormalitas terendah 25,25 ± 2,22%.

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ABSTRACTCryopreservation is a method of storing genetic material at low temperatures for long periods of time. One of the benefits of cryopreservation is to overcome the problem of population decline. The kancra fish is one of the species of the Cyprinidae family whose population is declining so that conservation efforts are needed. One of the factors that influence the success of cryopreservation is cryoprotectant. Natural cryoprotectants are used because they have lower toxicity than cryoprotectants from chemicals. Egg yolk is a natural cryoprotectant that can maintain cells during the cryopreservation process. The purpose of this study is to evaluate the effect of egg yolk as natural cryoprotectants on motility, viability, abnormalities, and fertilization of 48-hour spermatozoa after cryopreservation. Concentrations of free-range chicken egg yolk used are: 0%, 5%, 10%, 15%, 20% and 25%. The ratio used for sperm dilution is 1:10. Data analysis using the ANAVA test and then followed by the Tukey test. Based on the results of the one-way ANAVA test, it was found that cryoprotectant of free-range chicken egg yolk combined with 10% methanol had an effect (P <0.05) on motility, viability, abnormality, and fertility of post-cryoprotected spermatozoa. Egg yolk concentration of 5% was the optimum concentration that can maintain the highest percentage of motility, viability and fertility, respectively 84.06 ± 1.67%, 82.13 ± 1.75% and 92.96 ± 1.94% and the percentage value the lowest abnormality was 25.25 ± 2.22%."

"ABSTRAKIkan kancra merupakan salah satu spesies air tawar di Indonesia yang populasinya terus terancam. Upaya yang dapat dilakukan untuk melestarikan material genetik hewan yang terancam punah yaitu kriopreservasi spermatozoa. Salah satu faktor yang menentukan keberhasilan kriopreservasi adalah krioprotektan. Salah satu krioprotektan alami potensial yaitu kuning telur puyuh. Tujuan dari penelitian ini yaitu mengevaluasi konsentrasi optimal dari berbagai konsentrasi kuning telur puyuh (0%, 5%, 10%, 15%, 20%, dan 25%) terhadap motilitas, viabilitas, abnormalitas dan kemampuan fertilisasi spermatozoa ikan kancra 48 jam pascakriopreservasi. Rasio antara semen dan larutan pengencer yang digunakan yaitu 1:10. Analisis data menggunakan uji ANAVA satu arah dan dilanjutkan dengan uji Tukey. Berdasarkan hasil uji ANAVA, pemberian berbagai konsentrasi kuning telur puyuh yang dikombinasikan dengan metanol 10% menghasilkan pengaruh nyata (P<0,05) terhadap persentase motilitas, viabilitas, abnormalitas, dan fertilitas spermatozoa pascakriopreservasi. Kuning telur 10% merupakan konsentrasi optimal yang dapat mempertahankan persentase motilitas, viabilitas, dan fertilitas tertinggi yaitu masing-masing 85,10 ± 1,51%, 84,75 ± 1,71% dan 95,00 ± 1,83% serta menghasilkan nilai persentase abnormalitas terendah yaitu 20,25 ± 1,71%.

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ABSTRACTKancra fish is one of the freshwater species in Indonesia, whose population is continues to be threatened. The efforts that can be done to preserve the endangered animal's genetic material are cryopreservation of spermatozoa. One of the factors that determines the success of cryopreservation is cryoprotectant. One of the potential natural cryoprotectants is quail egg yolks. The purpose of this research is to evaluate the optimal concentration of various concentrations of quail egg yolks (0%, 5%, 10%, 15%, 20%, and 25%) on motility, viability, abnormality and fertilization ability of kancra fish spermatozoa 48 hours post-cryopreservation. The ratio between semen and diluent solution used was 1:10. Data was analyzed using one-way ANOVA test and continued with the Tukey test. Based on the results of the one-way ANOVA test, it was found that cryoprotectant of quail egg yolk combined with 10% methanol had significant effect (P <0.05) on motility, viability, abnormality, and fertility of spermatozoa post-cryopreservation. The 10% of quail egg yolk concentration was the optimal concentration that could maintain the highest percentage of motility, viability and fertility, respectively 85.10 ± 1.51%, 84.75 ± 1.71%, 95.00 ± 1.83% and produced the lowest percentage value of abnormality 20.25 ± 1.71%."

"ABSTRAKKriopreservasi merupakan metode penyimpanan material genetik pada suhu rendah dalam jangka waktu tertentu. Kriopreservasi spermatozoa dapat digunakan sebagai usaha konservasi ex situ ikan kancra (Tor soro) yang populasinya semakin menurun. Pemilihan krioprotektan yang tepat dapat meminimalkan kerusakan akibat terbentuknya kristal es dan mempertahankan kualitas spermatozoa selama kriopreservasi. Gula merah sebagai krioprotektan alami dan metanol 10% memiliki potensi untuk kriopreservasi spermatozoa ikan kancra. Tujuan penelitian yaitu mendapatkan konsentrasi optimal dari berbagai konsentrasi gula merah dan metanol 10% terhadap motilitas, viabilitas, dan abnormalitas spermatozoa pascakriopreservasi ikan kancra, serta mengevaluasi persentase fertilitas spermatozoa pascakriopreservasi ikan kancra. Konsentrasi gula merah yang digunakan yaitu 0%, 5%, 10%, 15%, 20%, dan 25%. Rasio antara semen dan larutan pengencer yang digunakan yaitu 1:10. Ekuilibrasi dilakukan pada suhu 5 °C selama 10 menit. Pembekuan dilakukan pada suhu -10 °C selama 48 jam. Pencairan dilakukan pada suhu 40 °C selama 60 detik. Analisis data dilakukan dengan menggunakan uji ANAVA yang dilanjutkan dengan uji Tukey. Hasil penelitian menunjukkan bahwa krioprotektan gula merah memberikan pengaruh (P<0,05) pada kualitas spermatozoa pascakriopreservasi. Krioprotektan gula merah 15% dan metanol 10% menghasilkan persentase motilitas (81,85 ± 1,11%), viabilitas (83,75 ± 1,71%), fertilitas (89,75 ± 1,71%) tertinggi, serta abnormalitas terendah (14,50 ± 1,73%) pada spermatozoa pascakriopreservasi.

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ABSTRACTCryopreservation is a method of storing genetic material at low temperatures for a certain period of time. Spermatozoa cryopreservation can be used as an ex situ conservation method for kancra fish (Tor soro) whose population is declining. Selection of the right cryoprotectant can minimize damage caused by the formation of ice crystals and maintain the quality of spermatozoa during cryopreservation. Brown sugar as natural cryoprotectant and 10% methanol have potential for cryopreservation of spermatozoa. The research objective was to obtain the optimal concentration of various concentrations of brown sugar and 10% methanol on the motility, viability, and abnormalities of kancra fish spermatozoa after cryopreservation, and evaluate the fertility of kancra fish spermatozoa after cryopreservation. The concentration of brown sugar used were 0%, 5%, 10%, 15%, 20%, and 25%. The ratio between semen and diluent solution used was 1:10. Equilibration was carried out at 5 °C for 10 minutes. Freezing was carried out at -10 °C for 48 hours. Thawing was done at 40 °C for 60 seconds. Data was analyzed using ANOVA test followed by Tukey test. The results showed that the cryoprotectant brown sugar had an significant influence (P<0.05) on the quality of post-cryopreserved spermatozoa. 15% brown sugar together with 10% methanol can produce the highest percentage of motility (81.85 ± 1.11%), viability (83.75 ± 1.71%), fertility (89.75 ± 1.71%), and the lowest abnormality (14.50 ± 1.73%) in spermatozoa post-cryopreservation."