Call number: LD2668 .T4 1956 H86 / Master of Science

Call number: LD2668 .T4 1979 S34 / Master of Science

Master of Science / Department of Animal Sciences and Industry / Karol E. Fike / David M. Grieger / Synchronizing estrus before AI is an effective way to shorten the breeding season, and increasing the number of pregnancies per AI may lead to greater use and acceptance of synchronization protocols among beef producers. Our objective was to determine if pregnancy rates to fixed-time AI (FTAI) would be improved by delaying insemination in heifers not expressing estrus before FTAI in a 7-d CO-Synch + controlled internal drug release (CIDR) estrus-synchronization protocol. In Experiment 1, yearling beef heifers (n = 465) at three locations of commercial and purebred herds were treated with GnRH (Cystorelin 100 µg im) and a CIDR insert (1.38 g of progesterone) on Day 0. On Day 7 CIDR inserts were removed and all heifers received PGF[subscript]2α (Lutalyse 25 mg im) and were fitted with an estrus-detection patch (Estrotect; Rockway, Inc.). Heifers were assigned to three treatments based on estrus-detection patch color at 48 h after PGF[subscript]2α: (1). Estrus-Red 48 h (Red 48; n = 180), heifers that expressed estrus and were inseminated at 48 h; (2). Non-Estrus-Gray 48 h (Gray 48; n = 137) heifers that did not express estrus and were inseminated at 48 h; and (3). Non-Estrus Delayed- 56 h (Gray 56; n = 148), heifers that did not express estrus at 48 h, and were not inseminated until 56 h after PGF[subscript]2α. Pregnancy rate to AI was greatest (P < 0.0001) for Red 48 heifers (67.8%) compared with heifers in the Gray 48 (39.4%) and Gray 56 (42.6%) treatments. Heifers assigned to Gray 48 and Gray 56 achieved similar (P = 0.83) pregnancy rates. In Experiment 2, yearling beef heifers (n = 257) at two different locations were treated with the same 7-d CO-Synch protocol, but heifers were assigned to three different treatments based on estrus-detection patch color at 48 h after PGF[subscript]2α: (1). Estrus-Red 48 h (Red 48; n =95), heifers that expressed estrus and were inseminated at 48 h; (2). Non-Estrus-Gray 48 h (Gray 48; n = 84), heifers that did not express estrus but were inseminated at 48 h; and (3). Non-Estrus Delayed- 72 h (Gray 72; n = 78), heifers that did not express estrus at 48 h, and were not inseminated until 72 h after PGF[subscript]2α. Pregnancy rate to AI was greatest (P = 0.004) for Red 48 heifers (62.1%) compared with heifers in Gray 48 (40.5%), and Gray 72 (46.2%). No difference in pregnancy rates (P = 0.75) was detected between heifers assigned to treatments Gray 48 and Gray 72. Delaying insemination in heifers not expressing estrus by 48 h after PGF[subscript]2α did not improve pregnancy rates to AI.

No description available.

No description available.

Includes bibliographical references (leaves 274-316) Examines several aspects of male reproduction in the sheep, and how these are related to fertility in the female when semen is introduced by natural mating or artificial insemination.

Includes bibliographical references (leaves 274-316) / xxii, 333 leaves : ill. (chiefly col.) ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Examines several aspects of male reproduction in the sheep, and how these are related to fertility in the female when semen is introduced by natural mating or artificial insemination. / Thesis (Ph.D.)--University of Adelaide, Dept. of Animal Sciences, 1991

Objectives were to 1) evaluate the use of the CO-Synch + CIDR (COS-C) protocol for synchronization of ovulation and timed AI (TAI) in Bos indicus-influenced cattle, 2) compare cumulative pregnancy rates after COS-C synchronization and TAI to those in a traditional management (TM) scheme, and 3) evaluate specific ovarian, hormonal, and estrual events associated with COS-C. The COS-C regimen included insertion of a controlled internal drug release device (CIDR) containing progesterone and injection of GnRH (GnRH-1) on day 0, removal of the CIDR and injection of prostaglandin F2a (PGF on d 7, and injection of GnRH (GnRH-2) and TAI 48 h later. In experiment 1 (Exp. 1), 335 females were stratified by BCS, parity and d postpartum before random assignment to COS-C or TM. An additional 96 females in which TM controls were not available for comparison also received COS-C. Conception rates to TAI averaged 39% (n = 266). Cumulative pregnancy rates were greater (P < 0.05) after 30 and 60 d of the breeding season in COS-C than in TM (n = 170 and 165 females respectively). In experiment 2 (Exp. 2), 100 postpartum (F1) females were stratified as in Exp. 1 within four replicates (25 each) and assigned randomly to receive either COSC or COS (no CIDR) treatment. No differences were observed between treatments and all data were pooled. Percentages of cows ovulating after GnRH-1, developing a synchronized follicular wave, exhibiting luteal regression to PGF, and ovulating to GnRH-2 were 40, 60, 93, and 72%, respectively. In experiment 3 (Exp. 3), primiparous (F1) heifers (n = 32) and pluriparous cows (n = 18) received the Select Synch + CIDR synchronization regimen (no GnRH-2 or TAI). Mean intervals from CIDR removal to estrus and ovulation, and from estrus to ovulation were 70 ± 2.9, 99 ± 2.8, and 29 ± 2.2 h, respectively. Relatively low TAI conception rates (< 50%) were attributed to failure of 40% of cattle to develop a synchronized follicular wave after GnRH-1 and to inappropriate timing of TAI/GnRH-2. It may be possible to improve TAI conception rates by delaying TAI/GnRH-2 to between 66 and 72 h, and by developing methods to increase the number of ovulations after GnRH-1.

Thesis (M. Phil.)--University of Hong Kong, 2001. / Includes bibliographical references (leaves 149-174).

The objective of this study was to develop a reliable method for intracytoplasmic sperm injection (ICSI) in bovine oocytes. Oocytes recovered from abattoir-derived ovaries were centrifuged for 5 min at 6000xg to facilitate sperm injection. Sperm were pre-treated in vitro with 5mM dithiothreitol (DTT), and diluted (approximately 1:5) with 5% polyvinylpyrrolidone (PVP) in 0.9% saline. After sperm injection, various activation procedures were compared. Initially, 3 h after activation with 5muM Ionomycin (A23187), oocytes with second polar bodies were selected and treated with 1.9mM 6-dimethylaminopurine (DMAP). The cleavage rate of sperm-injected oocytes treated with Ionomycin and DMAP was higher than with Ionomycin alone (62.1 vs. 27.3%, p < 0.05). In sham-injected control oocytes treated with Ionomycin and DMAP, the cleavage rate was approximately six times higher than that of oocytes treated with Ionomycin alone (44.3 vs. 7.4%, p < 0.001). Upon examination 16 h after ICSI, pronuclear formation was observed in 33 of 47 (70.2%) DMAP-treated oocytes. Two pronuclei were present in 18 of 33 (54.6%), while one and three pronuclei were seen in 8 of 33 (24.2%) and 7 of 33 (21.2%), respectively. In sham-injected DMAP-treated control oocytes, 6 of 15 (40.0%) had one pronucleus while 9 of 15 (60.0%) had two pronuclei. Since a single Ca2+ stimulation provided insufficient activation and DMAP treatment could result in triploidy, activation by multiple Ca2+ stimulations following ICSI was tested. Three Ca2+ stimulations were given at 30-min intervals. Pronuclear formation was observed in 16 of 41 (39.0%) oocytes at 16 h after sperm injection, with one and two pronuclei found in 4 of 16 (25.0%) and 12 of 16 (75.0%), respectively. Although one pronucleus was formed in 3 of 33 (9.1%) sham-injected control oocytes treated with three Ca2+ stimulations, two pronuclei were not seen in any of these oocytes. Due to the low rate of pronuclear formation after 5muM Ionomycin, 50muM