Theses and Dissertations

Permanent URI for this collection

https://univendspace.univen.ac.za/handle/11602/2210

Browse

Browsing Theses and Dissertations by Issue Date

Filter results by year or month
Now showing 1 - 20 of 46
  • Thumbnail Image
    ItemOpen Access
  • Thumbnail Image
    ItemOpen Access
    Milk yield and quality, nitrogen metabolism and rumen fermentation parameters in dairy cows fed different level of dietary concentrate and live yeast
    (2015) Shabangu, Nomthandazo Petronella; Baloyi, J. J.; Muya, M. C.
    The overall objective of this study was to investigate the effects of level of dietary concentrate and live yeast (LY) on milk yield, milk composition, rumen fermentation and nitrogen metabolism in lactating dairy cows. Four primiparous Holstein dairy cows in early lactation (average weight 500 ±9 kg and 20 days in milk (DIM)) were used in a 4 x 4 Latin Square design for a period of 44 days. The animals had seven days of adaptation to the treatments and four days for measurements. The treatments were, Low concentrate to forage (C:F) diet (40:60) with no additive, High C:F diet (60:40) with no additive, High C:F diet with LY and Low C:F diet with LY.Cows weremilked at 06h00 and 16h00 daily and milk samples were analysed for fat, protein, lactose milk urea nitrogen (MUN) and somatic cell count (SCC). Proximate analysis of feed samples was done and daily feed intake was recorded. Weight and body condition score were determined at beginning and end of every experimental period. Faecal and urinary nitrogen (N)were determined. In vitro batch fermentation was conducted to determine ruminal fermentation kinetics. Data generated from the feeding trial was analysed for a 4 x 4 Latin square design (LSD) using the PROC MIXED procedure of SAS (2009) and data for the invitro trialwassubjected to ANOVA using PROC GLM (SAS Institute, 2009) for a complete randomized design. Addition of LY affected only dry matter intake (DMI) (P<0.05), which effect was pronounce when cows were fed low (40:60) C:F diet resulting in better feed efficiency(FE). Cows fed high C:F diet consumed more feed, produced more milk with high fat and protein content (P<0.05). Both LY and C:F reduced (P<0.05) N intake as result of low DMI, but reduced (P<0.05) N excretion in manure. Addition of LY decreased ruminal ammonia and increased total VFA’s (P<0.05). The effects on ammonia suggest a better utilisation of diet proteins and probably more incorporation of products of CP degradation into microbial proteins, which support the observed reduced manure N excretion. The opposite was observed with high C:F diet, which increased ammonia and decreased total VFA’s. Propionate and butyrate were increased and decreased, respectively by high C:F diet.Addition of LY reduced SCC and MUN compared to control.The effects of LY were better pronounced on most parameters at low C:F diet. It is therefore recommended that the effects of LY be tested at low C:F on a larger scale of animals over longer periods to observe its effect of the rest of the parameters.
  • Thumbnail Image
    ItemOpen Access
  • Thumbnail Image
    ItemOpen Access
    Effects of stocking density, genotype and sex on the growth performance and carcass characteristics of Ross and Cobb broilers chickens
    (2015-05) Siaga, Rudzani; Beny, K.; Baloyi, J. J.
    See the attached abstract below
  • Thumbnail Image
    ItemOpen Access
    Comparative evaluation of different extenders of bull semen stored under different conditions
    (2015-07-16) Raseona, Andrea Motswetla; Barry, D. M.; Nedambale, T. L.
    Preservation of semen is an important process to ensure that semen quality is sufficient for use in assisted reproductive technologies. This study evaluated the effectiveness of three different extenders to preserve bull semen stored under different conditions, as an alternative to frozen-thawed semen straws used for artificial insemination. Semen samples were collected from two Nguni bulls using an electro-ejaculator and transported to the laboratory at 37 °C for evaluation. Pooled semen was first aliquoted into three extenders namely Triladyl, Ham’s F10 and M199 at a dilution ratio of 1:4 (semen:extender), and then stored at controlled room temperature 24 °C. Secondly pooled semen was aliquoted into four groups of Ham’s F10 extender and diluted at a ratio of 1:4, then stored at 24 °C, 17 °C, 12 °C and 5 °C respectively. Sperm motility rates were analysed after 0, 24, 48 and 72 hours. Morphology, viability and sperm DNA fragmentation were analysed after 72 hours. The study was replicated four times and data was analysed by ANOVA. Triladyl had higher sperm viability rate and total motility rate for 72 hours (P<0.01). However, Ham’s F10 had higher progressive motility rate as compared to the other extenders. There was no significant difference (P<0.01), in the viability rate between Ham’s F10 and M199. No significant difference was also observed in total sperm abnormalities (absent tails, coiled tails and bent tails), except for reacted acrosomes (P>0.05), between the two Nguni bulls. Lower temperatures than 24 °C influenced sperm motility and viability in Ham’s F10. There was no significant difference in sperm DNA fragmentation rates (P<0.01), between all the four storage temperatures which indicated that temperature did not have an influence on sperm DNA fragmentation. In conclusion, bull semen can be preserved in Triladyl or Ham’s F10 and M199 culture media stored at 24 °C and stay alive for 72 hours. Triladyl proved to be the best suitable extender showing higher sperm viability and total motility rates as compared to Ham’s F10 and M199. Lower temperatures than 24 °C noticeably decreased sperm motility and viability in Ham’s F10 culture medium.
  • No Thumbnail Available
    ItemOpen Access
  • Thumbnail Image
    ItemOpen Access
  • Thumbnail Image
    ItemOpen Access
    Comparison of progestone, PGF2A & NOVEL NC SYNCH GnRH based synchronization protocols in boer and indigenous goats of South Africa
    (2016-02-10) Dara, Onayi Brighton; Barry, D. M.; Baloyi, J. J.; Dondofema, Farai
  • Thumbnail Image
    ItemOpen Access
  • Thumbnail Image
    ItemOpen Access
    Efficiency of protein utilization of forage legumes for milk production on goats
    (2016-02-11) Katsande, Simbarashe; Baloyo, J. J.; Ngongoni, N. T.; Matope, G.; Nherera-Chokuda, F. V.
  • Thumbnail Image
    ItemOpen Access
  • Thumbnail Image
    ItemOpen Access
    Effect of different culture media and incubation methods on culturing murine embryos in vitro using a semen straw as an alternative receptacle
    (2016-05) Madzhie, Lufuno Rosheen; Barry, D. M.; Nedambale, T. L.
    See the attached abstract below
  • Thumbnail Image
    ItemOpen Access
    The effects of fertilization with bio-digester slurry and the inclusion of carbohydrate additives at ensiling on the nutritive value of Napier grass (pennisetum purpureum) silage
    (2016-05) Rambau, Mashudu Daniel; Baloyi, I. J.; Puchai, F.
    The objective of the study was to determine the effects of fertilisation with bio-digester slurry and the inclusion of carbohydrate additives at ensiling on the fermentation characteristics, chemical composition, ruminal degradability, and in vitro digestibility of Napier grass silage. Napier grass planted at the School of Agriculture Experimental Farm, University of Venda in 5 m x 4 m plots replicated three times in a completely randomised design and was irrigated with either biodigester slurry or no bio-digester slurry (tap water) for a period of 12 weeks. After 12 weeks, the Napier was freshly cut and ensiled for 90 days in 1 litre glass jars in a 2 (Control - tap water and slurry irrigation) x 4 (No additive, molasses, maize meal and brown sugar) factorial arrangement. Fermentation quality and nutritive composition were determined using standard protocols. The dry matter (DM) and crude protein (CP) ruminal degradability was determined in sacco by incubating feed samples in nylon bags (external dimension: 6 × 12 cm, pore size of 46 μm) in the rumen in three Bonsmara steers fitted with rumen cannulae for 0, 6, 12, 24, 48, 72, 96 and 120 hours (h). Parameters to describe the dynamics of ruminal degradability of DM and CP were obtained by fitting the data on the exponential equation P = a + b (1 - e-ct) using the NEWAY computer program, where “a” is the rapidly degradable fraction, “b” is the slowly degradable fraction and “c” is the outflow rate. The in vitro DM and CP degradability of rumen undegradable residue collected after 12, 24 and 48 h incubation was determined by sequential digestion in pepsin (abomasal) and pancreatin (small intestine) solutions. Fertilisation with bio-digester slurry increased (P <0.05) CP content of fresh cut Napier grass pre-ensilage. Bio-digester slurry fertilisation with molasses inclusion improved (P <0.05) the silage DM content which improved (P >0.05) fermentation characteristics with pH of 4.2 and lowest NH3-N of 13.3 g/kg. Other chemical compositions and fermentation characteristics were not affected (P >0.05) due to fertilisation x additives treatment combinations. No bio-digester slurry fertilisation with maize meal inclusion increased (P <0.01) DM degradability at 0 h incubation. As time progressed to 24 h, no biodigester slurry fertilisation with no additive included reduced (P <0.01) DM degradability with no difference (P >0.05) on other treatments. Potential DM degradability (a + b) of no bio-digester slurry fertilisation with no additive inclusion silage was reduced (P <0.01). The reduction was associated with low levels (P <0.01) of slowly degradable fraction “b”. In vitro DM and CP digestibility were not affected (P >0.05) due to fertilisation x additives treatment combinations. In conclusion, bio-digester slurry application improved the quality of fresh cut Napier grass, with the combination of bio-digester slurry fertilisation and molasses addition yielding the best silage quality.
  • Thumbnail Image
    ItemOpen Access
    Comparison of two different media and assisted hatching techniques on the embryo hatching rate using the mouse as a model
    (2017-05-18) Negota, Nkhumeleni Cathbert; Barry, D. M.; Nedambale. T. L.
    The use of in vitro culture media and assisted hatching techniques remain a challenging obstacle to hatching of blastocyst-stage embryos. Mechanical, chemical, enzymatic thinning and laser assisted techniques have been used previously, but there is still a lack of information on its application and implication in livestock. The aim of this study was to compare the effect of two in vitro culture media ((Ham’s F10 and Tissue Culture Medium 199 (TCM-199)) and four assisted hatching techniques (mechanical, chemical, enzymatic and laser) on blastocyst formation and hatching rate using murine embryos as a model. The C57BL/6 and BALB/c mouse breeds were bred and raised until they reach maturity and then bred naturally to produce a hybrid F1 generation. The light in the breeder house was controlled at 14 hours light and 10 hours darkness. Feed and water were provided ad libitum for the mice. Mature female mice were super-ovulated using equine chorionic gonadotropin (eCG) and human chorionic gonadotropin (hCG). A total of 400 blastocysts were collected from the F1 generation and these were allocated equally for the four assisted hatching techniques (laser, mechanical, chemical and enzymatic) as well as a non-treated control group. The blastocysts were paired into a group of 10 and replicated 4-four times for each assisted hatching techniques and control group. The embryos were then cultured for 24 hours and the hatching of the embryos were observed. Hatched embryos were stained for blastomere counting. The general linear model (GLM) of statistical analysis software (SAS) version 9.4 was used to analyze the data. Assisted hatching techniques (laser, mechanical, enzymatic and chemical) yielded 46.86±37.12; 51.07±40.19; 39.05±35.83 and 33.32±37.50% of hatching, respectively under in vitro culture in Ham’s F10. There was a significant difference (p<0.05) observed between assisted hatching techniques using Ham’s F10 as culture medium. In the TCM-199, laser, mechanical, enzymatic and chemical assisted hatching techniques yielded 56.25±43.30; 52.55±35.50; 49.16±37.50 and 33.85±35.50%, respectively, with significant differences (p<0.05). However, the hatching rate of embryos for all techniques was higher when in vitro cultured in TCM-199 compared to those cultured in Ham’s F10, and statistically higher than the control group. In conclusion, laser assisted hatching technique is the best of the techniques to use to assist the hatching of murine embryos and TCM-199 is the best of the two in vitro culture media for the hatching percentage.
  • Thumbnail Image
    ItemOpen Access
    Effect of bioxcell and triladyl extenders and removal of seminal plasma of equilibrated and cryopreserved goat semen
    (2017-05-18) Nethenzheni, Livhuwani Pertunia; Barry, D. M.; Nedambale, T. L.
    The objectives of the study were to evaluate the effect of two extenders (Triladyl® and Bioxcell®) and the removal of seminal plasma on goat buck semen. Six ejaculates were collected from six indigenous bucks by means of electro-ejaculator method, and semen was pooled, and replicated 10 times. Raw semen were randomly allocated into six groups as follows: (i) Raw non-washed, (ii) Raw washed, (iii) Triladyl®-washed, (iv) Triladyl®-non-washed, (v) Bioxcell®-washed and (vi) Bioxcell®-non-washed. All six groups were analysed for spermatozoa motility rates using computer-aided sperm analysis (CASA). The spermatozoa viability for all groups were assessed using Eosin-Nigrosin, acrosome integrity using Spermac, chromatin structure using Acridine Orange, and mitochondria using JC-1 staining solutions. Both the Triladyl® and Bioxcell® washed semen groups were diluted (1:4) with Phosphate Buffered Saline (PBS) then centrifuged at 1500 x g for ten min and seminal plasma was aspirated using 1 mL sterile plastic pipette. Semen samples were diluted (1:4) as follows: Triladyl® (washed and non-washed) or Bioxcell® (washed and non-washed) and then equilibrated at 5 ºC for 2 hours. Following equilibration, semen parameters were analysed. Thereafter, the semen samples were loaded into straws and placed 5 cm above a liquid nitrogen vapour for 10 min, and then stored at -196 ºC until use. Following one month of storage, frozen semen straws per treatment group were thawed at 37 ºC for 30 seconds, then semen parameters were analysed again. Significant differences among the mean values of semen parameters were determined by Tukey’s test using ANOVA, GLM procedure of SAS version 12.1 of 2010. Total Spermatozoa motility rate of Bioxcell® (92.5±4.6), (68.2±13.5) and Triladyl® (94.9±5.5), (63.1±15.1) were significantly reduced (P < 0.05) following equilibration and freeze-thawing process, respectively on washed semen groups. Live and normal spermatozoa percentages were drastically reduced in Bioxcell® (5.2±4.9) and Triladyl® (6.9±8.6) washed semen groups, following freeze-thawing. There was a significantly lower number of spermatozoa with high mitochondrial membrane potential in non-washed semen extended with Triladyl® (68.7±26.8) compared to non-washed semen extended with Bioxcell® (49.8±20.1) following the freeze-thawing process. In conclusion, the freezing-thawing process did reduce the indigenous buck semen parameters irrespective of removal or non-removal of seminal plasma. However, Bioxcell® extender was found to be more suitable for preserving spermatozoa during equilibration and freezing/thawing process of buck semen.
  • Thumbnail Image
    ItemOpen Access
    Genetic Parameter Estimates of Milkability Traits in South African Holstein Cattle
    (2017-09-18) Tshilate, Thendo Stanley; Bhebhe, E.; Banga, C. B.
    Milkability, or ease of milking, is the rate at which milk can be completely drawn from a cow’s udder. It is an important functional trait with regard to milking costs as well as udder health. Milkability traits have not been included in the breeding objectives of South African dairy cattle and their genetic parameters in the population have not been estimated. The primary objective of the study was to estimate genetic parameters for milkability traits in South African Holstein cattle. Data consisted of production and milkability records of 1 532 Holstein cows, from 6 herds, participating in the South African National Dairy Animal Recording and Improvement Scheme during the period 2015 to 2016 . Measures of milkability were average milk flow (AMF), maximum milk flow (MMF) and milking time (MT). Genetic parameters were estimated by a multi-trait sire model using the Restricted Maximum Likelihood (REML) procedure. Means for AMF, MMF and MT were 1.99 kg/min, 3.02 kg/min and 5.50 min, respectively. Non-genetic factors affecting variation in milkability traits were herd-year-season of calving, parity and milk yield. Heritability estimates for AMF, MMF, and MT were 0.23±0.09, h2 = 0.41±0.12 and h2 = 0.36±0.11, respectively. Genetic correlations between the three milkability traits were medium to high, ranging from -0.35±0.23 between AMF and MT to 0.79±0.09 between AMF and MMF. Correlations were positive between AMF and MMF and negative between MT and the other two traits. There was an increase in the mean EBV for AMF of 0.002 kg/min (0.0001 kg/min per year) during the period 2002 to 2014. Maximum milk flow also showed an increasing genetic trend of 0.04 kg/min (0.0003 kg/min per year) over the same period. The genetic trend for MT was undesirable, as it increased by 0.0003 kg/min. There is scope for improving milkability through selection, in South African Holstein cattle, as indicated by the moderate to high heritability estimates. The favourable genetic correlations among milkability traits imply that selection on one trait will result in a correlated improvement in the others. Results of the current study provide a basis for including milkability traits in the breeding objective for South African Holstein cattle.
  • Thumbnail Image
    ItemOpen Access
    Effects of different inclusion levels of marula (sclerocarya birrea) pulp at ensiling on the nutritive value of Napier grass (pennisetum purpureum) silage
    (2017-09-18) Makharamedzha, Unarine; Baloyi, J. J.; Mikasi, M. S.
    See the attached abstract below
  • Thumbnail Image
    ItemOpen Access
    Evaluation of Nguni bull semen-extended in tris egg yolk extender, soybean milk and coconut water based extenders and stored at different temperatures
    (2017-09-18) Mayombo, Pie Veillard Kalonji; Barry, D. M.; Owiny, D. O.
    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.
  • Thumbnail Image
    ItemOpen Access
    Evaluation of suitable chilled, extended semen preservation time and their effects of different artificial insemination techniques on the fertility of indigenous Venda goats
    (2017-09-18) Monyeleote, Vukosi; Barry, D. M.; Fushai, F.; Bhehbe, E.
    The aims of the study were to evaluate the effects of dilution and chilled storage time on the quality of semen, and of different artificial insemination techniques on fertility in artificially inseminated indigenous Venda does. Fresh semen was collected using an artificial vagina from three Boer bucks aged 4±1.55 years once every four days during July and August 2016. Semen was pooled and samples were divided into two equal parts, which were extended using Biladyl® extender at ratios of 1:5 and 1:10 v/v (semen to extender), before refrigeration for 120 hours at 5 °C. The fresh undiluted semen and freshly extended semen were evaluated in six replicates for sperm motility, live-dead and sperm morphology using the Sperm Class Analyzer (SCA). Extended semen continued to be evaluated at 24 hour intervals for 120 hours. Ninety indigenous Venda does were obtained from different flocks in the Vhembe district and kept intensively in one 10 m x 40 m pen at the University of Venda experimental farm in the goat feedlot. The does were fed and watered ad libitum. After acclimatization for 14 days, estrus was synchronized using a controlled internal drug release (CIDR) containing 0.3 g of progesterone. Upon removal of the CIDR, does were injected 10 mg of PGF2α (Lutalyse® dinoprost tromethamine) Sterile Solution. At 24 hours after the removal of the CIDR, the does were injected intramuscularly with 300 international units (IU) of equine chorionic gonadotrophin (eCG). Forty eight hours after the removal of the progesterone, freshly collected and diluted (1:5 ratio ~150x106 sperm/ml), five day-stored semen were used to inseminate the does using cervical (CAI), trans-cervical (TAI), and laparoscopic artificial (LAI) insemination methods in a complete randomized design (CRD) with a 2 X 3 factorial arrangement of the treatments with 15 replications per treatment. The does were tested for pregnancy after 30 days using ultrasonography. Analyses of variance was performed on the pregnancy, kidding rates and on prolificacy using the GLM procedure of Minitab (Minitab 2013). Significant differences in all motility parameters were observed between the extension ratios and storage time (P<0.01). There were significant interactions between the extension ratio and storage time (P<0.05) on the sub-population of sperm cells with non-progressive motility (NON-P). Significant (P<0.01) interaction was observed between the semen extension ratio and storage time on medium and slow spermatozoa (P<0.01). The method of insemination did not (P>0.05) affect fertility, though both pregnancy and kidding rates numerically decreased in the order laparoscopic insemination (LAI)≥ trans-cervical insemination (TAI)≥ cervical insemination (CAI). Overall, 71% kidding rate was achieved.
  • Thumbnail Image
    ItemOpen Access
    The efficiency of ultrasonorgraphy in monitoring ovarian structures and foetal development in goats, sheep and cattle as verified through laparoscopy and laparotomy
    (2018-05-18) Siphugu, Steven Mbonalo; Barry, D. M.; Mashiloane, M. L.
    The main purpose of this study was to assess the efficiency of ultrasonography in monitoring reproductive organs, pregnancy diagnosis, and foetal gender identification and to verify its reliability by laparoscopy and laparotomy, where applicable. Reproductive organs, pregnancy diagnosis and gender of the foetus were examined by A-mode ultrasound using 3.0 - 8.0 MHz trans-rectal transducer. A Sony Olympus Model laparoscope with a camera transducer was used to monitor the reproductive organs and pregnancy diagnosis. In monitoring the follicular dynamics, daily ultrasonography (ULTS) scanning was done for 17 days in sheep and for 21 days in both goats and cattle. Follicles of diameter ≥ 3 mm were selected for analysis of growth, ovulation and regression. For determining the efficiency of the techniques, laparoscopy (LAPSC) and laparotomy (LAPT) were used on days 3 and 10 of the goats and sheep oestrous cycle. The follicles were grouped into three categories according to their diameter as 3 - 4.9 mm, 5 - 7.9 mm and ≥ 8 mm, whereas the follicles of cattle were grouped as 3 - 4.9 mm, 5 - 9.9 mm and ≥ 10 mm. Early pregnancy diagnosis examinations were carried out from day 18 post insemination until pregnancy was confirmed. Foetal gender examinations were conducted from day 40 of pregnancy until the day the gender of the foetus was confirmed. Follicular development was accompanied by the occurrence of waves of follicular growth at different period of the oestrous cycle. The first follicular wave emerged on day 1.0 ± 0.4 in goats, 1.2 ± 0.4 in sheep and 2.2 ± 0.4 in cattle. The maximum diameter of the dominant follicles of observed follicular waves in goats was 7.3 ± 0.4 mm, 6.6 ± 0.2 mm, 7.3 ± 0.2 mm; in sheep was 6.4 ± 0.4 mm, 6.6 ± 0.4 mm and 6.7 ± 0.7 mm and in cattle was 13.1 ± 0.8 mm, 14.2 ± 0.6 mm and 15.7 ± 0.6 mm in wave 1, 2 and 3, respectively. However, the maximum size of the dominant follicle of the ovulatory wave in cattle was larger than the dominant follicles of both first and second waves, but in goats and sheep the dominant follicles were of similar size throughout the waves. In cattle, the ovulatory wave was shorter (p ˂ 0.05) than the duration of the first and second waves, while in sheep and goats were similar throughout the waves. In goats the total number of follicles counted in right and left ovaries under category 3 - 4.9 mm was lower with ULTS and LAPSC than with LAPT method (p ˂ 0.05). In sheep the mean number of follicles between 3 - 4.9 mm category in both right and left ovaries were different (p ˂ 0.05) between ULTS and LAPT. However, for categories 5 - 7.9 mm and ≥ 8 mm in both goats and sheep the mean numbers of follicles observed by all techniques were similar (p ˃ 0.05). In goats, pregnancy diagnosis accuracy improved from zero percent on day 18 to 100% on day 26 - 28, in sheep pregnancy diagnosis was 40% on day 18 and improved to 100% on day 20 - 22 vi of gestation. In cattle accuracy of pregnancy diagnosis was not possible at day 18 and gradually increased to 100% on day 30 - 32 of gestation. Out of 5 (100%) goat’s foetuses whose gender was determined, the diagnosis was correct in 100% (3/3) of the male foetuses and 100% (2/2) of the female foetuses. In sheep two foetuses were sexed as males while the other three were sexed as females and were both 100%. Out of 60% (3/5) of foetuses examined in cattle, 1 (100%) was identified as male and the remaining 2 (100%) were identified as females. The results obtained confirmed that the accuracy for foetal gender by ultrasonography was 100% in all foetuses observed. The current study demonstrated that trans-rectal ultrasonography examination is an efficient method for monitoring follicular dynamics, diagnosing pregnancy and foetal gender identification and that it is as reliable as laparoscopy and laparotomy where they were applied together.