Breeding Season in Female Cats Acclimated Under a Natural Photoperiod and Interval Until Puberty

2004 ◽  
Vol 66 (9) ◽  
pp. 1129-1132 ◽  
Author(s):  
Toshihiko TSUTSUI ◽  
Kiyoshi NAKAGAWA ◽  
Taichi HIRANO ◽  
Keiichi NAGAKUBO ◽  
Masakazu SHINOMIYA ◽  
...  
Author(s):  
S. Wigzell ◽  
J.J. Robinson ◽  
J.M. Wallace ◽  
R.P. Aitken

Daily oral dosing in mid afternoon with 3 mg of the indoleamine, melatonin, from early June onwards is highly effective in advancing the breeding season of both Greyface and Scottish Blackface ewes kept under a natural photoperiod; the mean reaction interval from initial dosing to the onset of ovarian activity in Scottish Blackface ewes being around 65 days compared with 110 days for untreated controls (Robinson et al 1985). Advancing the starting time for the melatonin treatment to mid-March gave a similar reaction interval with behavioural oestrus occurring in late May/early June (Wigzell et al 1986a). Following this reversal of the breeding season by melatonin, continued melatonin treatment in unmated ewes resulted in a period of oestrous cyclicity lasting 4 to 5 months. Thereafter the ewes became refractory to melatonin and returned to anoestrus at a time when untreated controls were commencing ovarian activity (Wigzell et al 1986b). These observations prompted us to investigate the effects of different durations of melatonin treatment on ovarian activity.


Reproduction ◽  
2002 ◽  
pp. 269-280 ◽  
Author(s):  
LM Sanford ◽  
CA Price ◽  
DG Leggee ◽  
SJ Baker ◽  
TA Yarney

The regulation of inhibin secretion has not been elucidated fully in male ruminants. The aim of this study was to determine the relative importance of FSH and testosterone concentrations, and FSH receptors, in the control of secretion of immunoactive inhibin in rams. In Expt 1, temporal changes in hormone concentrations and testicular FSH binding were determined for two groups of rams (n = 4) kept under opposite, alternating 4 month periods of long (16 h light:8 h dark) and short (8 h light:16 h dark) days. Testicular biopsies (1-2 g) were collected when the testes were regressed, redeveloping, redeveloped and regressing. In Expt 2, separate groups of rams (n = 4) kept under natural photoperiod (latitude 45 degrees 48 minutes N) were designated as controls or passively immunized (for 3 weeks) with sufficient oestradiol antiserum to increase testosterone secretion without altering LH and FSH; this was done when the testes were regressed (non-breeding season) and redeveloped (breeding season). In both groups of rams (Expt 1), 'seasonal' increases in FSH concentrations began a few weeks earlier than did increases in inhibin concentrations. FSH reached maximum concentrations during testicular recrudescence, whereas numbers of FSH receptors in the testis and circulatory inhibin concentrations did not reach peak values until the testes were fully developed. Numbers of FSH receptors per testis, but not FSH concentration, were positively correlated (r = 0.65) with inhibin concentrations across the four stages of the testicular cycle. Near the end of testicular recrudescence early in the breeding season (Expt 2), relatively high FSH concentration was associated with increased abundance of FSH receptor mRNA (90%) and number of receptors (45%) in the testis and increased inhibin concentrations (50%), compared with when the testes were regressed. Moderate, physiological increases in testosterone secretion in immunized rams did not affect inhibin in either season. These results indicate that: (i) FSH stimulation of immunoactive inhibin secretion by Sertoli cells as testes recrudesce is via increases in secretion (early) and cognate receptors (late); (ii) FSH upregulates the synthesis of its own receptor late in recrudescence; and (iii) the positive correlation (r = 0.70) observed between circulatory testosterone and immunoactive inhibin does not reflect a causal relationship.


1996 ◽  
Vol 62 (3) ◽  
pp. 507-512 ◽  
Author(s):  
T. Sweeney ◽  
D. O'Callaghan

AbstractWhile the onset of the breeding season in ewes can be advanced up to 7 weeks following exposure to long days (44 days) before lambing, a melatonin implant from lambing and exposure to a ram from the summer solstice, this advance is reduced by the absence of a ram. The aim of this experiment was to determine if earlier exposure to the ram and/or exposure to more long days before lambing would further advance the onset of the breeding season. A further aim was to compare the ovulation rate and duration of the breeding season between ewes with a normal and advanced onset of the breeding season due to this treatment regime. Pregnant ewes lambing in mid March were allocated to treatments as follows: (1) controls, maintained on natural photoperiod; (2) 44 LD + mel, exposed to 44 long days (18L: 6D; LD) before lambing followed by a 700-mg melatonin implant after lambing; (3) 90 LD + mel, as in treatment 2, but exposed to 90 LD before lambing; (4) 90 LD + mel + ram, as in treatment 3, including continuous exposure to a vasectomized ram from 10 April. Reproductive state was assessed from serum progesterone concentrations in blood collected at 3- to 4-day intervals from 10 April and ovulation rate was determined during the luteal phase of the first five oestrous cycles in control ewes and ewes exposed to 90 LD + mel + ram. Ewes exposed to 90 LD + mel + ram commenced the breeding season 10 weeks earlier (median date 25 July, range 28 days;P< 0·001) than controls (median date 8 October, range 68 days). Overall, the onset of the breeding season was not advanced in ewes given 44 or 90 LD + mel in the absence of a ram, but a biphasic response was evident, with 40 to 50% of ewes beginning the breeding season at the same time as ewes on 90 LD + mel + ram. Ovulation rate was similar between control ewes and ewes exposed to 90 LD + mel + ram (P > 0·05). The duration of the breeding season was longer in ewes exposed to 90 LD + mel + ram (210 (s.e. 15) days;P< 0·002) than in control ewes (158 (s.e. 10) days), with no difference in date of the end of the breeding season (P > 0·05). Exposure of ewes to 90 LD before lambing in March, followed by a melatonin implant and exposure to the ram from 10 April advanced the onset and extended the duration of the breeding season without an overall effect on ovulation rate. The ram is an important component of this signal sequence.


1999 ◽  
Vol 69 (1) ◽  
pp. 217-222 ◽  
Author(s):  
L. M. Mitchell ◽  
M. E. King ◽  
R. P. Aitken ◽  
J. M. Wallace

AbstractThe objective was to determine the effect of previous lambing date and subsequent month of mating on reproductive performance in Mule (Bluefaced Leicester × Scottish Blackface) ewes. Sixty-four ewes which had previously lambed in January (13 January (s.e. = 1 day)) and 80 ewes which had previously lambed in May (15 May (s.e. = 1 day)) were allocated equally to four mating periods (30 August to 17 September, 1 November to 19 November, 3 January to 21 January and 14 February to 4 March) in a 2 × 4 factorial design. From 20 days before and during their designated mating period, January- and May-lambing ewes were separately housed in straw-bedded pens under natural photoperiod and were given 1 kg per head per day dried grass pellets. A vasectomized ram was continuously present with each group for 17 days and was replaced by a raddled, fertility tested entire Suffolk ram at the start of the mating period. Ewes were mated at a single natural oestrus and those marked by the ram were recorded daily. Ovulation rate was measured by laparoscopy on day 6 after mating. For ewes which had previously lambed in January (16 per group), numbers by month of mating that showed oestrous behaviour, ovulated and were pregnant, respectively, were: September, 16, 15 and 12; November, 16, 15 and 14; January, 15, 15 and 10 and February, 15, 16 and 7. Mean (s.e.) ovulation rates by month of mating were 2·1 (0.16), 2·5 (0.19), 2·1 (0.09) and 2·2 (0.19) corpora lutea per ewe ovulating, and lambing rates by month of mating were 1·3 (0.25), 1·9 (0.25), 1·2 (0.24) and 0·8 (0.23) lambs per ewe to the ram. For ewes which had previously lambed in May (20 per group), numbers by month of mating that showed oestrous behaviour, ovulated and were pregnant, respectively, were: September, 13, 20 and 12; November, 20, 20 and 19; January, 20, 20 and 17 and February, 20, 20 and 13. Mean (s.e.) ovulation rates by month of mating were 2·0 (0.13), 2·3 (0.11), 2·1 (0.05) and 2·2 (0.11) corpora lutea per ewe ovulating, and lambing rates by month of mating were 1·0 (0.21), 2·1 (0.15), 1·5 (0.17) and 1·2 (0.21) lambs per ewe to the ram. Ovulation, pregnancy and lambing rates were not influenced by previous lambing date, but lambing rates were significantly (P < 0·01) reduced for ewes mated in September and February compared with November. Results demonstrate that in Mule ewes acceptable ovulation rates can be achieved throughout the period September to February but lambing rates are reduced when ewes are mated at the extremes of their natural breeding season. The main factor contributing to the reduction in lambing rates was an increase in the number of ewes failing to establish pregnancy as a consequence of ovulation without oestrous behaviour, fertilization failure and (or) total embryo loss.


2021 ◽  
Author(s):  
Azhar F. Abdel Fattah ◽  
Noura E. Abd Elhameed ◽  
Elshimaa M. Roushdy ◽  
Mohamed S. El Kholy ◽  
Mahmoud Alagawany

2017 ◽  
Vol 17 (1) ◽  
pp. 25-32
Author(s):  
Jacinta Lalchhanhimi ◽  
Lalremsanga H.T.

The breeding biology of tree frog, Polypedates teraiensis was studied during the breeding season at Mizoram University Campus. It was found that sound production by male during the breeding season was primarily a reproductive function and advertisement calls attract females to the breeding areas and announce other males that a given territory is occupied. The aim of this study was to provide the detailed information on the breeding behaviour and the advertisement calls of Polypedates teraiensis. The morphometric measurements of the amplecting pairs (males and females) for sexual dimorphism along with clutch sizes were also studied.


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