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Статті в журналах з теми "Bulls Spermatozoa Storage"
Zakharchuk, D. "SPERM PRODUCTIVITY AND FERTILIZATION CAPACITY OF SPERMATOZOA OF HOLSTEIN STUD BULLS IN CONDITIONS OF LLC “UKRAINIAN GENETIC COMPANY”." Animal Breeding and Genetics 62 (December 8, 2021): 136–44. http://dx.doi.org/10.31073/abg.62.18.
Повний текст джерелаChrenek, P., E. Spaleková, L. Olexikova, A. Makarevich, and E. Kubovicova. "Quality of Pinzgau bull spermatozoa following different periods of cryostorage." Zygote 25, no. 2 (March 9, 2017): 215–21. http://dx.doi.org/10.1017/s0967199417000077.
Повний текст джерелаBochenek, M., and Z. Smorag. "258 THE EFFECT OF A PLANT PROTEIN COMPONENT OF MEDIA USED FOR BULL SPERM SEXING ON SPERM MEMBRANE STATUS." Reproduction, Fertility and Development 20, no. 1 (2008): 209. http://dx.doi.org/10.1071/rdv20n1ab258.
Повний текст джерелаBrillianti, Febby Fairy, Pudji Srianto, Trilas Sardjito, Tri Wahyu Suprayogi, Indah Norma Triana, and Dadik Rahardjo. "Kualitas semen sapi pejantan berdasarkan umur, suhu, dan kelembaban di Taman Ternak Pendidikan Universitas Airlangga." Ovozoa : Journal of Animal Reproduction 10, no. 3 (December 1, 2021): 81. http://dx.doi.org/10.20473/ovz.v10i3.2021.81-89.
Повний текст джерелаPero, M. E., G. J. Killian, P. Lombardi, L. Zicarelli, L. Avallone, and B. Gasparrini. "327 IDENTIFICATION OF OSTEOPONTIN IN WATER BUFFALO SEMEN." Reproduction, Fertility and Development 19, no. 1 (2007): 279. http://dx.doi.org/10.1071/rdv19n1ab327.
Повний текст джерелаKhaled Taïbi, Mohamed Achir,, Leila Ait Abderrahim, Mohamed Boussaid, Kada Souana, Abdelkader Tadj, Toufik Benaissa, and Tayeb Gouchich. "Dissecting the relationship between artificial insemination success and bull semen quality in the arid region of Tiaret (Algeria)." Bionatura 7, no. 1 (February 15, 2022): 1–5. http://dx.doi.org/10.21931/rb/2022.07.01.18.
Повний текст джерелаSusandani, Oky, Tri Wahyu Suprayogi, Ratna Damayanti, and Anwar Ma'ruf. "Factors Affecting Fresh Semen Quality in Pasundan Cattle at UPTD BPPIBTSP Ciamis." Journal of Applied Veterinary Science And Technology 2, no. 2 (October 30, 2021): 37. http://dx.doi.org/10.20473/javest.v2.i2.2021.37-42.
Повний текст джерелаMalcotti, V., V. Pelufo, N. Bergamo, and E. Aisen. "Recovery of epididymal spermatozoa from bull and red deer, stored at different times and temperatures before freezing - thawing." Animal Production Science 52, no. 8 (2012): 741. http://dx.doi.org/10.1071/an11366.
Повний текст джерелаAmorim, E. A. M., J. K. Graham, M. Meyers, and B. Spizziri. "67 DELIVERING CHOLESTANOL OR DESMOSTEROL TO BULL SPERM MEMBRANES IMPROVES CRYOSURVIVAL." Reproduction, Fertility and Development 20, no. 1 (2008): 114. http://dx.doi.org/10.1071/rdv20n1ab67.
Повний текст джерелаDurfey, C. L., T. Rowlison, C. U. Lagu, C. Sente, M. L. Khaitsa, H. J. Clemente, P. L. Ryan, S. T. Willard, and J. M. Feugang. "111 Improvement of cat and bull sperm quality using nanotechnology as a model for wild species." Reproduction, Fertility and Development 31, no. 1 (2019): 181. http://dx.doi.org/10.1071/rdv31n1ab111.
Повний текст джерелаДисертації з теми "Bulls Spermatozoa Storage"
Mayombo, Pie Veillard Kalonji. "Evaluation of Nguni bull semen-extended in tris egg yolk extender, soybean milk and coconut water based extenders and stored at different temperatures." Diss., 2017. http://hdl.handle.net/11602/880.
Повний текст джерелаDepartment of Animal Science
In order to realize many of the potential advantages of AI, storage of semen is necessary. Semen storage is only possible using a system that decreases and/or halts the metabolic processes of the spermatozoa, allowing no significant loss of fertility. Numerous factors affect the success of spermatozoa storage. This study was designed to compare the effects of egg yolk, soybean milk and coconut water in Tris extender using different storage methods for Nguni bull spermatozoa storage. Bull semen was collected from two adult Nguni bulls approximately four years old and kept under similar managerial conditions. Using electro-ejaculator, semen was collected from each bull into a graduated semen collection tube. Macroscopically evaluation of the sample was performed immediately after collection. Only the semen free from contamination was processed. The kinetic properties namely: total spermatozoa motility, and progressive spermatozoa motility were analysed using CASA. Semen sample was stained and spermatozoa morphology and vitality also analysed using CASA. The extended semen was then split into three groups. The first group was stored at room temperature (25 °C). The second group was cooled to 4 °C and stored in the refrigerator. The third group was also cooled to 4 °C for 2 h in the refrigerator, then held in LN2 vapour 5 cm above the surface of LN2 at ~ -80 °C for 10 min and then plunged into LN2 for storage at -196 °C. Different colours of straws and plugging powder were used for identifying each extender. After 3 days of storage at room temperature, in the refrigerator and in LN2, the extended semen was split into three portions and assayed for kinetic properties using the first portion. The second portion was assayed for spermatozoa morphology and the third portion for spermatozoa vitality. The results from the fresh semen extended with all three extenders (TEYE, SBME and COWE), and analysed immediately after dilution at room temperature (25 ºC), showed no significant difference (P > 0.05) in the mean values of the kinetic and morphologic properties and viability, on spermatozoa TM, PM, AR, AT, CT; BT and LS. After three days of storage, there was no significant difference (P > 0.05) in the kinetic morphologic properties and viability of semen stored at room and refrigeration temperature regardless of the extender in use. There were, however, significant differences (P < 0.05) in the TM, PM, AR and DL of the frozen semen samples. For the short storage period of semen used for AI, from this study, it is recommended that semen should be kept at room or refrigeration temperature regardless of the three extenders used. However, for long storage of frozen semen TEYE is recommended. The egg yolk-based extender provided greater preservation of motility and bull spermatozoa integrity during the freezing process than did SBME and COWE.