Mate preference does not influence reproductive motivation and parental cooperation in female zebra finches

In socially monogamous species, low availability of sexually active unpaired individuals in the local population may constrain mate choice, resulting in mating with sub-optimal partners. Here we experimentally investigate whether female reproductive behaviour is different when paired with a preferred or a non-preferred male in the zebra finch (Taeniopygia guttata). First, we assessed female mating preferences using a four-way choice apparatus, then females were caged together with either their preferred or least-preferred male. Female reproductive motivation, assessed by the propensity of laying eggs within two weeks from pairing and clutch mass, did not differ between the two experimental groups. Females responded to mate removal by either increasing their care, so as to compensate for the lost care of their mate, or by significantly reducing incubation. This bimodal response was not explained by mate preference, nevertheless, we found that females with lower baseline (i.e., pre-manipulation) incubation effort were more likely to cease incubation during mate removal. Taken together, we found no evidence that female reproductive behaviour varies along with mate preference.

The effect of mate removal on dawn singing behaviour in male pied bush chats

To determine the influence of pairing status on dawn singing behaviour in pied bush chats Saxicola caprata, we conducted mate removal experiments across eight territories. The experiment was divided into three stages: pre-removal (pairs were present on their respective territories), removal (females were experimentally removed), and returned (females were released into the focal pairs’ territories). Dawn bout length, song rate, song complexity, percentage performance time, song perch height, and distance of singing location to territory boundary were measured for each male during each experimental stage. We did not find an effect of mate removal on any dawn song characteristics of male pied bush chats suggesting that the presence or absence of a mate does not influence male dawn singing behaviour. Our findings further suggest that males use dawn chorus to mediate social relationships with neighbouring males to proclaim an established territory.

16 MODIFICATION TO INTRAVAGINAL PROGESTERONE + ESTRADIOL-BASED ESTROUS SYNCHRONIZATION PROTOCOLS TO IMPROVE OVARIAN RESPONSES IN BOS INDICUS HEIFERS

Estrous synchronization (ES) protocols for fixed-time AI (FTAI) have been mainly developed for Bos taurus cattle assuming that usage in Bos indicus cattle results in similar outcomes. Unexplained variation in the reproductive outcomes of these treatments in extensively managed Bos indicus herds has limited the adoption of FTAI. The aim was to evaluate the ovarian function in heifers treated with different doses of progesterone (P4). Brahman (n = 30) and Brahman-cross (n = 34; 3/4 to 7/8 Brahman) heifers weighing an average of 285 kg (248 to 323 kg) and 307 kg (250 to 363 kg), respectively, were allocated at random to 1 of 4 treatment groups: 1) full-dose Cue-Mate (CM100; two P4-impregnated pods, 1.56 g of P4; Bioniche Animal Health Aust/Asia, Armidale, NSW, Australia; n = 17); 2) half-dose Cue-Mate (CM50; one P4-impregnated pod; 0.78 g of P4; n = 15); 3) half-dose Cue-Mate + 300IU of eCG (CM50+G; Pregnecol, Bioniche Animal Health, Aust/Asia; n = 14) i.m. at Cue-Mate removal; and 4) double PGF2α group (PG; n = 18). Heifers in the P4-treated groups received 1 mg of EB (estradiol benzoate; Ciderol; 1 mg mL-1; Genetics Australia, Bacchus Marsh, Victoria) at Cue-Mate insertion (Day -10) and 24 h after Cue-Mate removal (Day -1) and 250 μg of PGF2α (Cloprostenol, Estromil, Ilium Veterinary Products, Smithfield, Australia) i.m. at Cue-Mate insertion (Day -10) and removal (Day -2). Heifers in the PG group received 500 μg of PGF2α on Day -16 and Day -2 i.m. Ovarian function was evaluated twice daily by transrectal ultrasonography on Day -1, Day 0 (expected estrus), and Day 1, and once daily on Days 4, 6, 8, 10, 12, and 16 of the synchronized and return cycles. Concurrent blood samples were collected to determine plasma P4 concentrations. A one-way ANOVA was used to analyze follicle diameter variables and Fisher’s Exact test was used to analyze all other data reported (StataCorp 2007, College Station, TX, USA). There was no difference (P = 0.31) in the diameter of the dominant follicle 54 to 56 h post-Cue-Mate removal (the time FTAI would be conducted) in the CM100 (11.5 ± 1.1), CM50 (13.3 ± 1.5), CM50+G (13.7 ± 1.5), or PG (14.5 ± 0.7) groups. Synchrony of ovulation in ovulating heifers did not differ (P < 0.05) between the P4-treated groups with 12/13 (CM100), 11/12 (CM50), and 9/12 (CM50+G) heifers ovulating within 53 to 77 h after Cue-Mate removal, but was lower (P < 0.02) for the PG group (1/5). Individual heifer P4 profiles revealed that 2/15, 1/15, 3/12, and 0/5 of heifers that ovulated in the CM100, CM50, CM50+G, andPG groups, respectively, failed to re-ovulate in the return cycle. Also, 1/15, 3/15, 1/12, and 0/5 of heifers that ovulated in the CM100, CM50, CM50+G, and PG groups, respectively, developed a CL that persisted into the return cycle. This study shows the potential benefits of using intravaginal devices containing a lower amount of P4 to induce synchronized ovulation in Brahman heifers, consistent with the findings of Carvalho et al. (2008 Theriogenology 69, 167).