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The Banteng (Bos javanicus d'Alton 1823) is an endemic species in Indonesia that is threatened with extinction and whose population continues to decline in the wild. The aim of this study is to determine the timing of artificial insemination (AI) in the Banteng based on follicle size and uterine enlargement. For this study, two female Banteng were used in Taman Safari Indonesia, Cisarua, Bogor. Habituation was performed to facilitate data collection. Optimal timing for AI is determined by examining the reproductive organs using Ultrasonography (USG) to detect changes in the uterus and ovaries and monitor clinical signs of estrus. Follicle size and uterine examination was performed on days -1, 0, and +1 for 3 estrus cycles. Insemination was performed 2-3 times during estrus until ovulation occurred. The results showed that the average follicle size of both Banteng was 1.09 ± 0.02 cm on day -1, 1.31 ± 0.02 cm on day 0, and 1.33 ± 0.03 cm on day +1. Artificial insemination was performed with a double dose of frozen semen when the Banteng were still rideable, and the follicle size ranged from 1.23-1.38 cm. Pregnancy was examined by ultrasound on day 21 after mating; both Banteng females were pregnant after AI. It can be concluded that AI technique can be used in captive Banteng breeding program by studying the development of follicles and uterine enlargement. [ABSTRACT FROM AUTHOR]

Background and Aim: The Javan leopard (Panthera pardus melas Cuvier, 1809) is a subspecies of Panthera pardus spp., spread across the African and Asian regions. Information on reproductive aspects is crucial for wild animals, including the Javan leopard. In this study, we aimed to develop electroejaculator (EE) techniques and evaluate cryopreservation success in Javan leopard semen. Materials and Methods: The semen of four adult Javan leopards was collected once a week using EE. Placement of the EE probe in the rectum was performed after ultrasound imaging (ultrasonography) to determine the prostate body location. The semen obtained was then evaluated macroscopically and microscopically. Three Javan leopards were used for cryopreservation. The ejaculate was divided into two parts [i.e., one part diluted with AndroMed® (Minitüb, Tiefenbach, Germany) and the other part with Steridyl® (Minitüb)] at a 1:1 ratio immediately after collection and evaluation. The semen was then packed in a 0.25 mL MiniStraw® (Minitüb) then equilibrated at 4°C for 2 h. After equilibration, the straw was then frozen in liquid nitrogen vapor. Frozen semen was then stored in containers until further evaluation. Results: The results showed that ejaculation response occurred at all levels of stimulation, while erections did not always occur. The fastest ejaculation and erection occurred at the fourth voltage. The macroscopic evaluation showed that the semen volume was 0.80±0.26 mL, cloudy white, pH 7.44±0.14, and with watery semen consistency. The microscopic evaluation showed that the sperm motility was 66.98±0.39%, with sperm viability of 75.6±1.79%. Sperm concentration was 62.17±46.95x106 mL-1 with a total concentration of 42.14±23.51x106 cells. Normal sperm morphology is only 40.72±6.26%. Conclusion: This study concluded that the development of a semen collection technique using an EE preceded by imaging of the EE probe location using ultrasound was effective for the ejaculation of Javan leopards. The characteristics of the semen of the Javan leopard showed moderate semen volume, sperm motility, and viability. Javan leopard showed low sperm concentration and normal sperm morphology. [ABSTRACT FROM AUTHOR]