Effect of follicle age on conception rate in beef heifers1

The objective of this study was to determine the effect of age of the ovulatory follicle on fertility in beef heifers. Ovulation was synchronized with the 5 d CO-Synch + controlled intravaginal drug release (CIDR) program in heifers in Montana (MT; n = 162, Hereford and Angus Crossbred) and Ohio (OH...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of animal science 2014-03, Vol.92 (3), p.1022-1028
Hauptverfasser: Abreu, F. M., Cruppe, L. H., Maquivar, M., Utt, M. D., Madsen, C. A., Vasconcelos, J. L. M., Mussard, M. L., Day, M. L., Geary, T. W.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1028
container_issue 3
container_start_page 1022
container_title Journal of animal science
container_volume 92
creator Abreu, F. M.
Cruppe, L. H.
Maquivar, M.
Utt, M. D.
Madsen, C. A.
Vasconcelos, J. L. M.
Mussard, M. L.
Day, M. L.
Geary, T. W.
description The objective of this study was to determine the effect of age of the ovulatory follicle on fertility in beef heifers. Ovulation was synchronized with the 5 d CO-Synch + controlled intravaginal drug release (CIDR) program in heifers in Montana (MT; n = 162, Hereford and Angus Crossbred) and Ohio (OH; n = 170, Angus Crossbred). All heifers received estradiol benzoate (EB; 1 mg/500 kg BW, [i.m.]) 6 d after the final GnRH of the synchronization program to induce follicular atresia and emergence of a new follicular wave (NFW) followed by prostaglandin F2... (PGF2...; 25 mg, i.m.) administration either 5 d ("young" follicle [YF]; n = 158) or 9 d ("mature" follicle [MF]; n = 174) after EB. Estrous detection was performed for 5 d after PGF2α with AI approximately 12 h after onset of estrus. Ovarian ultrasonography (MT location only) was performed in YF and MF at EB, 5 d after EB, PGF2α, and AI. Heifers in MT (n = 20) and OH (n = 18) that were not presynchronized or did not initiate a NFW were excluded from further analyses, resulting in 142 and 152 heifers in MT and OH, respectively. Heifers from the MF treatment in MT that initiated a second NFW after EB but before PGF2α (MF2; n = 14) were excluded from the primary The objective of this study was to determine The objective of this study was to determine the effect of age of the ovulatory follicle on fertility in beef heifers. Ovulation was synchronized with the 5 d CO-Synch + controlled intravaginal drug release (CIDR) program in heifers in Montana (MT; n = 162, Hereford and Angus Crossbred) and Ohio (OH; n = 170, Angus Crossbred). All heifers received estradiol benzoate (EB; 1 mg/500 kg BW, [i.m.]) 6 d after the final GnRH of the synchronization program to induce follicular atresia and emergence of a new follicular wave (NFW) followed by prostaglandin F2... (PGF2...; 25 mg, i.m.) administration either 5 d ("young" follicle [YF]; n = 158) or 9 d ("mature" follicle [MF]; n = 174) after EB. Estrous detection was performed for 5 d after PGF2α with AI approximately 12 h after onset of estrus. Ovarian ultrasonography (MT location only) was performed in YF and MF at EB, 5 d after EB, PGF2α, and AI. Heifers in MT (n = 20) and OH (n = 18) that were not presynchronized or did not initiate a NFW were excluded from further analyses, resulting in 142 and 152 heifers in MT and OH, respectively. Heifers from the MF treatment in MT that initiated a second NFW after EB but before PGF2α (MF2; n = 14) were excluded from the priwa
doi_str_mv 10.2527/jas.2013-6761
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1511119760</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3259743361</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1760-8eefa7d10f86d054e550a1d2e3a25fa2922bd29121f3043724d0f876821c46ac3</originalsourceid><addsrcrecordid>eNotkD1PwzAQhi0EEqUwsltidvGdYydhQ1X5kCqxwGy5zhlShTjY6cC_x1W55W543nulh7FbkCvUWN_vXV6hBCVMbeCMLUCjFgqMOmcLKRFE0wBesquc91IC6lYv2MMmBPIzj4GHOAy9H4i7T-Jx5D6Onqa5L2dyM_F-5DuiwL-oD5QyXLOL4IZMN_97yT6eNu_rF7F9e35dP26Fh9pI0ZSMqzuQoTGd1BVpLR10SMqhDg5bxF2HLSAEJStVY9UVtDYNgq-M82rJ7k5_pxR_DpRnu4-HNJZKCxrKtKWmUOJE-RRzThTslPpvl34tSHvUY4see9Rjj3rUH69cVcg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1511119760</pqid></control><display><type>article</type><title>Effect of follicle age on conception rate in beef heifers1</title><source>Oxford University Press Journals All Titles (1996-Current)</source><creator>Abreu, F. M. ; Cruppe, L. H. ; Maquivar, M. ; Utt, M. D. ; Madsen, C. A. ; Vasconcelos, J. L. M. ; Mussard, M. L. ; Day, M. L. ; Geary, T. W.</creator><creatorcontrib>Abreu, F. M. ; Cruppe, L. H. ; Maquivar, M. ; Utt, M. D. ; Madsen, C. A. ; Vasconcelos, J. L. M. ; Mussard, M. L. ; Day, M. L. ; Geary, T. W.</creatorcontrib><description>The objective of this study was to determine the effect of age of the ovulatory follicle on fertility in beef heifers. Ovulation was synchronized with the 5 d CO-Synch + controlled intravaginal drug release (CIDR) program in heifers in Montana (MT; n = 162, Hereford and Angus Crossbred) and Ohio (OH; n = 170, Angus Crossbred). All heifers received estradiol benzoate (EB; 1 mg/500 kg BW, [i.m.]) 6 d after the final GnRH of the synchronization program to induce follicular atresia and emergence of a new follicular wave (NFW) followed by prostaglandin F2... (PGF2...; 25 mg, i.m.) administration either 5 d ("young" follicle [YF]; n = 158) or 9 d ("mature" follicle [MF]; n = 174) after EB. Estrous detection was performed for 5 d after PGF2α with AI approximately 12 h after onset of estrus. Ovarian ultrasonography (MT location only) was performed in YF and MF at EB, 5 d after EB, PGF2α, and AI. Heifers in MT (n = 20) and OH (n = 18) that were not presynchronized or did not initiate a NFW were excluded from further analyses, resulting in 142 and 152 heifers in MT and OH, respectively. Heifers from the MF treatment in MT that initiated a second NFW after EB but before PGF2α (MF2; n = 14) were excluded from the primary The objective of this study was to determine The objective of this study was to determine the effect of age of the ovulatory follicle on fertility in beef heifers. Ovulation was synchronized with the 5 d CO-Synch + controlled intravaginal drug release (CIDR) program in heifers in Montana (MT; n = 162, Hereford and Angus Crossbred) and Ohio (OH; n = 170, Angus Crossbred). All heifers received estradiol benzoate (EB; 1 mg/500 kg BW, [i.m.]) 6 d after the final GnRH of the synchronization program to induce follicular atresia and emergence of a new follicular wave (NFW) followed by prostaglandin F2... (PGF2...; 25 mg, i.m.) administration either 5 d ("young" follicle [YF]; n = 158) or 9 d ("mature" follicle [MF]; n = 174) after EB. Estrous detection was performed for 5 d after PGF2α with AI approximately 12 h after onset of estrus. Ovarian ultrasonography (MT location only) was performed in YF and MF at EB, 5 d after EB, PGF2α, and AI. Heifers in MT (n = 20) and OH (n = 18) that were not presynchronized or did not initiate a NFW were excluded from further analyses, resulting in 142 and 152 heifers in MT and OH, respectively. Heifers from the MF treatment in MT that initiated a second NFW after EB but before PGF2α (MF2; n = 14) were excluded from the priwas compared to MF and YF treatments in MT. Estrous response was similar (90%; 252/280) between treatments and locations. Proestrus interval (from PGF2α to estrus) and age of the ovulatory follicle at AI were similar for MF heifers between locations (54.6 ± 1.7 h and 8.3 ± 0.07 h) but were greater (P &lt; 0.01) for YF heifers in OH (78.5 ± 1.4 h and 5.3 ± 0.06 h) than MT (67.4 ± 1.6 h and 4.8 ± 0.06 h; treatment ... location, P &lt; 0.01). However, conception rate did not differ for MF (63.8%; 74/116) and YF (67.0%; 91/136) treatments. In the MT heifers, follicle size and follicle age at AI in the YF treatment (10.4 ± 0.15 mm and 4.8 ± 0.06 d, respectively) was less (P &lt; 0.01) than in the MF treatment (11.0 ± 0.18 mm and 8.3 ± 0.11 d, respectively), but conception rate to AI did not differ between treatments in MT. In the MF2 group proestrus interval was greater (P &lt; 0.01); hence, diameter of the ovulatory follicle and age were similar to that for the YF treatment. Conception rate to AI did not differ between MF2, MF, and YF (61.5, 63.3, and 64.7%, respectively) in MT. In conclusion, manipulation of age of the nonpersistent ovulatory follicle at spontaneous ovulation did not influence conception rate. (ProQuest: ... denotes formulae/symbols omitted.)</description><identifier>ISSN: 0021-8812</identifier><identifier>EISSN: 1525-3163</identifier><identifier>DOI: 10.2527/jas.2013-6761</identifier><language>eng</language><publisher>Champaign: Oxford University Press</publisher><subject>Animal reproduction ; Cattle ; Fertility ; Reproductive system</subject><ispartof>Journal of animal science, 2014-03, Vol.92 (3), p.1022-1028</ispartof><rights>Copyright American Society of Animal Science Mar 2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1760-8eefa7d10f86d054e550a1d2e3a25fa2922bd29121f3043724d0f876821c46ac3</citedby><cites>FETCH-LOGICAL-c1760-8eefa7d10f86d054e550a1d2e3a25fa2922bd29121f3043724d0f876821c46ac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Abreu, F. M.</creatorcontrib><creatorcontrib>Cruppe, L. H.</creatorcontrib><creatorcontrib>Maquivar, M.</creatorcontrib><creatorcontrib>Utt, M. D.</creatorcontrib><creatorcontrib>Madsen, C. A.</creatorcontrib><creatorcontrib>Vasconcelos, J. L. M.</creatorcontrib><creatorcontrib>Mussard, M. L.</creatorcontrib><creatorcontrib>Day, M. L.</creatorcontrib><creatorcontrib>Geary, T. W.</creatorcontrib><title>Effect of follicle age on conception rate in beef heifers1</title><title>Journal of animal science</title><description>The objective of this study was to determine the effect of age of the ovulatory follicle on fertility in beef heifers. Ovulation was synchronized with the 5 d CO-Synch + controlled intravaginal drug release (CIDR) program in heifers in Montana (MT; n = 162, Hereford and Angus Crossbred) and Ohio (OH; n = 170, Angus Crossbred). All heifers received estradiol benzoate (EB; 1 mg/500 kg BW, [i.m.]) 6 d after the final GnRH of the synchronization program to induce follicular atresia and emergence of a new follicular wave (NFW) followed by prostaglandin F2... (PGF2...; 25 mg, i.m.) administration either 5 d ("young" follicle [YF]; n = 158) or 9 d ("mature" follicle [MF]; n = 174) after EB. Estrous detection was performed for 5 d after PGF2α with AI approximately 12 h after onset of estrus. Ovarian ultrasonography (MT location only) was performed in YF and MF at EB, 5 d after EB, PGF2α, and AI. Heifers in MT (n = 20) and OH (n = 18) that were not presynchronized or did not initiate a NFW were excluded from further analyses, resulting in 142 and 152 heifers in MT and OH, respectively. Heifers from the MF treatment in MT that initiated a second NFW after EB but before PGF2α (MF2; n = 14) were excluded from the primary The objective of this study was to determine The objective of this study was to determine the effect of age of the ovulatory follicle on fertility in beef heifers. Ovulation was synchronized with the 5 d CO-Synch + controlled intravaginal drug release (CIDR) program in heifers in Montana (MT; n = 162, Hereford and Angus Crossbred) and Ohio (OH; n = 170, Angus Crossbred). All heifers received estradiol benzoate (EB; 1 mg/500 kg BW, [i.m.]) 6 d after the final GnRH of the synchronization program to induce follicular atresia and emergence of a new follicular wave (NFW) followed by prostaglandin F2... (PGF2...; 25 mg, i.m.) administration either 5 d ("young" follicle [YF]; n = 158) or 9 d ("mature" follicle [MF]; n = 174) after EB. Estrous detection was performed for 5 d after PGF2α with AI approximately 12 h after onset of estrus. Ovarian ultrasonography (MT location only) was performed in YF and MF at EB, 5 d after EB, PGF2α, and AI. Heifers in MT (n = 20) and OH (n = 18) that were not presynchronized or did not initiate a NFW were excluded from further analyses, resulting in 142 and 152 heifers in MT and OH, respectively. Heifers from the MF treatment in MT that initiated a second NFW after EB but before PGF2α (MF2; n = 14) were excluded from the priwas compared to MF and YF treatments in MT. Estrous response was similar (90%; 252/280) between treatments and locations. Proestrus interval (from PGF2α to estrus) and age of the ovulatory follicle at AI were similar for MF heifers between locations (54.6 ± 1.7 h and 8.3 ± 0.07 h) but were greater (P &lt; 0.01) for YF heifers in OH (78.5 ± 1.4 h and 5.3 ± 0.06 h) than MT (67.4 ± 1.6 h and 4.8 ± 0.06 h; treatment ... location, P &lt; 0.01). However, conception rate did not differ for MF (63.8%; 74/116) and YF (67.0%; 91/136) treatments. In the MT heifers, follicle size and follicle age at AI in the YF treatment (10.4 ± 0.15 mm and 4.8 ± 0.06 d, respectively) was less (P &lt; 0.01) than in the MF treatment (11.0 ± 0.18 mm and 8.3 ± 0.11 d, respectively), but conception rate to AI did not differ between treatments in MT. In the MF2 group proestrus interval was greater (P &lt; 0.01); hence, diameter of the ovulatory follicle and age were similar to that for the YF treatment. Conception rate to AI did not differ between MF2, MF, and YF (61.5, 63.3, and 64.7%, respectively) in MT. In conclusion, manipulation of age of the nonpersistent ovulatory follicle at spontaneous ovulation did not influence conception rate. (ProQuest: ... denotes formulae/symbols omitted.)</description><subject>Animal reproduction</subject><subject>Cattle</subject><subject>Fertility</subject><subject>Reproductive system</subject><issn>0021-8812</issn><issn>1525-3163</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNotkD1PwzAQhi0EEqUwsltidvGdYydhQ1X5kCqxwGy5zhlShTjY6cC_x1W55W543nulh7FbkCvUWN_vXV6hBCVMbeCMLUCjFgqMOmcLKRFE0wBesquc91IC6lYv2MMmBPIzj4GHOAy9H4i7T-Jx5D6Onqa5L2dyM_F-5DuiwL-oD5QyXLOL4IZMN_97yT6eNu_rF7F9e35dP26Fh9pI0ZSMqzuQoTGd1BVpLR10SMqhDg5bxF2HLSAEJStVY9UVtDYNgq-M82rJ7k5_pxR_DpRnu4-HNJZKCxrKtKWmUOJE-RRzThTslPpvl34tSHvUY4see9Rjj3rUH69cVcg</recordid><startdate>20140301</startdate><enddate>20140301</enddate><creator>Abreu, F. M.</creator><creator>Cruppe, L. H.</creator><creator>Maquivar, M.</creator><creator>Utt, M. D.</creator><creator>Madsen, C. A.</creator><creator>Vasconcelos, J. L. M.</creator><creator>Mussard, M. L.</creator><creator>Day, M. L.</creator><creator>Geary, T. W.</creator><general>Oxford University Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RQ</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>M7S</scope><scope>MBDVC</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>S0X</scope><scope>U9A</scope></search><sort><creationdate>20140301</creationdate><title>Effect of follicle age on conception rate in beef heifers1</title><author>Abreu, F. M. ; Cruppe, L. H. ; Maquivar, M. ; Utt, M. D. ; Madsen, C. A. ; Vasconcelos, J. L. M. ; Mussard, M. L. ; Day, M. L. ; Geary, T. W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1760-8eefa7d10f86d054e550a1d2e3a25fa2922bd29121f3043724d0f876821c46ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animal reproduction</topic><topic>Cattle</topic><topic>Fertility</topic><topic>Reproductive system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abreu, F. M.</creatorcontrib><creatorcontrib>Cruppe, L. H.</creatorcontrib><creatorcontrib>Maquivar, M.</creatorcontrib><creatorcontrib>Utt, M. D.</creatorcontrib><creatorcontrib>Madsen, C. A.</creatorcontrib><creatorcontrib>Vasconcelos, J. L. M.</creatorcontrib><creatorcontrib>Mussard, M. L.</creatorcontrib><creatorcontrib>Day, M. L.</creatorcontrib><creatorcontrib>Geary, T. W.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Career &amp; Technical Education Database</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection (ProQuest)</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database (ProQuest)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Research Library (Corporate)</collection><collection>Environmental Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><jtitle>Journal of animal science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abreu, F. M.</au><au>Cruppe, L. H.</au><au>Maquivar, M.</au><au>Utt, M. D.</au><au>Madsen, C. A.</au><au>Vasconcelos, J. L. M.</au><au>Mussard, M. L.</au><au>Day, M. L.</au><au>Geary, T. W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of follicle age on conception rate in beef heifers1</atitle><jtitle>Journal of animal science</jtitle><date>2014-03-01</date><risdate>2014</risdate><volume>92</volume><issue>3</issue><spage>1022</spage><epage>1028</epage><pages>1022-1028</pages><issn>0021-8812</issn><eissn>1525-3163</eissn><abstract>The objective of this study was to determine the effect of age of the ovulatory follicle on fertility in beef heifers. Ovulation was synchronized with the 5 d CO-Synch + controlled intravaginal drug release (CIDR) program in heifers in Montana (MT; n = 162, Hereford and Angus Crossbred) and Ohio (OH; n = 170, Angus Crossbred). All heifers received estradiol benzoate (EB; 1 mg/500 kg BW, [i.m.]) 6 d after the final GnRH of the synchronization program to induce follicular atresia and emergence of a new follicular wave (NFW) followed by prostaglandin F2... (PGF2...; 25 mg, i.m.) administration either 5 d ("young" follicle [YF]; n = 158) or 9 d ("mature" follicle [MF]; n = 174) after EB. Estrous detection was performed for 5 d after PGF2α with AI approximately 12 h after onset of estrus. Ovarian ultrasonography (MT location only) was performed in YF and MF at EB, 5 d after EB, PGF2α, and AI. Heifers in MT (n = 20) and OH (n = 18) that were not presynchronized or did not initiate a NFW were excluded from further analyses, resulting in 142 and 152 heifers in MT and OH, respectively. Heifers from the MF treatment in MT that initiated a second NFW after EB but before PGF2α (MF2; n = 14) were excluded from the primary The objective of this study was to determine The objective of this study was to determine the effect of age of the ovulatory follicle on fertility in beef heifers. Ovulation was synchronized with the 5 d CO-Synch + controlled intravaginal drug release (CIDR) program in heifers in Montana (MT; n = 162, Hereford and Angus Crossbred) and Ohio (OH; n = 170, Angus Crossbred). All heifers received estradiol benzoate (EB; 1 mg/500 kg BW, [i.m.]) 6 d after the final GnRH of the synchronization program to induce follicular atresia and emergence of a new follicular wave (NFW) followed by prostaglandin F2... (PGF2...; 25 mg, i.m.) administration either 5 d ("young" follicle [YF]; n = 158) or 9 d ("mature" follicle [MF]; n = 174) after EB. Estrous detection was performed for 5 d after PGF2α with AI approximately 12 h after onset of estrus. Ovarian ultrasonography (MT location only) was performed in YF and MF at EB, 5 d after EB, PGF2α, and AI. Heifers in MT (n = 20) and OH (n = 18) that were not presynchronized or did not initiate a NFW were excluded from further analyses, resulting in 142 and 152 heifers in MT and OH, respectively. Heifers from the MF treatment in MT that initiated a second NFW after EB but before PGF2α (MF2; n = 14) were excluded from the priwas compared to MF and YF treatments in MT. Estrous response was similar (90%; 252/280) between treatments and locations. Proestrus interval (from PGF2α to estrus) and age of the ovulatory follicle at AI were similar for MF heifers between locations (54.6 ± 1.7 h and 8.3 ± 0.07 h) but were greater (P &lt; 0.01) for YF heifers in OH (78.5 ± 1.4 h and 5.3 ± 0.06 h) than MT (67.4 ± 1.6 h and 4.8 ± 0.06 h; treatment ... location, P &lt; 0.01). However, conception rate did not differ for MF (63.8%; 74/116) and YF (67.0%; 91/136) treatments. In the MT heifers, follicle size and follicle age at AI in the YF treatment (10.4 ± 0.15 mm and 4.8 ± 0.06 d, respectively) was less (P &lt; 0.01) than in the MF treatment (11.0 ± 0.18 mm and 8.3 ± 0.11 d, respectively), but conception rate to AI did not differ between treatments in MT. In the MF2 group proestrus interval was greater (P &lt; 0.01); hence, diameter of the ovulatory follicle and age were similar to that for the YF treatment. Conception rate to AI did not differ between MF2, MF, and YF (61.5, 63.3, and 64.7%, respectively) in MT. In conclusion, manipulation of age of the nonpersistent ovulatory follicle at spontaneous ovulation did not influence conception rate. (ProQuest: ... denotes formulae/symbols omitted.)</abstract><cop>Champaign</cop><pub>Oxford University Press</pub><doi>10.2527/jas.2013-6761</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0021-8812
ispartof Journal of animal science, 2014-03, Vol.92 (3), p.1022-1028
issn 0021-8812
1525-3163
language eng
recordid cdi_proquest_journals_1511119760
source Oxford University Press Journals All Titles (1996-Current)
subjects Animal reproduction
Cattle
Fertility
Reproductive system
title Effect of follicle age on conception rate in beef heifers1
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T23%3A19%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effect%20of%20follicle%20age%20on%20conception%20rate%20in%20beef%20heifers1&rft.jtitle=Journal%20of%20animal%20science&rft.au=Abreu,%20F.%20M.&rft.date=2014-03-01&rft.volume=92&rft.issue=3&rft.spage=1022&rft.epage=1028&rft.pages=1022-1028&rft.issn=0021-8812&rft.eissn=1525-3163&rft_id=info:doi/10.2527/jas.2013-6761&rft_dat=%3Cproquest_cross%3E3259743361%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1511119760&rft_id=info:pmid/&rfr_iscdi=true