Reproduction in the Bridled Nailtail Wallaby, Onychogalea fraenata Gould (Marsupialia : Macropodidae), in Captivity

1997 ◽  
Vol 24 (4) ◽  
pp. 411 ◽  
Author(s):  
P. M. Johnson
Keyword(s):  
Post Partum ◽  
Oestrous Cycle ◽  
Gestation Period ◽  
Young Males ◽  
In Captivity ◽  
Males And Females ◽  
The Mean

The reproduction of the endangered macropod Onychogalea fraenata was studied in captivity. O. fraenata breeds throughout the year. A post-partum oestrus was not recorded, although mating during the pouch life was observed when the pouch young were 80–92 days old. The mean length of the oestrous cycle was determined to be 36·2 days, while the mean length of a gestation period was 23·6 days. Pouch life ranged between 119 and 126 days, and the young males and females matured as early as 270 days and 136 days, respectively.

Reproduction of the whiptail wallaby, Macropus parryi Bennett (Marsupialia : Macropodidae), in captivity with age estimation of the pouch-young

1998 ◽  
Vol 25 (6) ◽  
pp. 635 ◽  
Author(s):  
P. M. Johnson
Keyword(s):  
Age Estimation ◽  
Sexual Maturity ◽  
Post Partum ◽  
Age Determination ◽  
Oestrous Cycle ◽  
Gestation Period ◽  
Body Measurements ◽  
In Captivity ◽  
The Mean

Reproduction of the whiptail wallaby, Macropus parryi, was studied in captivity. The mean length of the oestrous cycle was 41.8 days while the mean length of the gestation period was 38.0 days. M. parryi bred throughout the year and post-partum oestrus was not recorded although mating did occur during the pouch life when the pouch-young was 118–168 days of age. The length of the pouch-life was 256–267 days and weaning occurred 104–215 days after emergence from the pouch. Sexual maturity for females occurred at 509–647 days of age. An age-determination table was produced and found useful for predicting age of pouch-young using body measurements.

Reproduction in the Plain Rock-Wallaby, Petrogale penicillata inornata Gould, in Captivity, with Age Estimation of the Pouch Young

1979 ◽  
Vol 6 (1) ◽  
pp. 1 ◽  
Author(s):  
PM Johnson
Keyword(s):  
Age Estimation ◽  
Post Partum ◽  
Oestrous Cycle ◽  
Gestation Period ◽  
In Captivity ◽  
Hind Foot ◽  
Males And Females ◽  
Premature Removal

'Reproduction in the plain rock-wallaby was studied in captivity. The oestrous cycle ranged from 30.2 to 32.0 days and the gestation period from 30.0 to 32.0 days. A post-partum mating usually followed birth; the resultant quiescent embryo developed and was born 28-30 days after premature removal of pouch young. The pouch life of the young ranged from 189 to 227 days, males and females maturing sexually at approximately 590 and 540 days respectively. Tail and hind foot lengths were found to be useful indicators of age of young up to the end of pouch life.

Reproduction in the red-legged pademelon, Thylogale stigmatica Gould (Marsupialia : Macropodidae), and age estimation and development of pouch young

1994 ◽  
Vol 21 (5) ◽  
pp. 553 ◽  
Author(s):  
PM Johnson ◽  
K Vernes
Keyword(s):  
Age Estimation ◽  
Post Partum ◽  
General Pattern ◽  
Age Determination ◽  
Gestation Period ◽  
Growth Equation ◽  
In Captivity ◽  
In The Wild ◽  
The Mean

The reproduction of Thylogale stigmatica in captivity was studied and a predictive growth equation for age determination of the pouch young was developed. The general pattern of reproduction involved an oestrous cycle of 29-32 days, a gestation period of 28-30 days and a mean pouch life of 184 days. A post-partum oestrus and mating generally followed birth. Births were observed in all months in captivity, and from October to June in the wild. Mean age of weaning of young was 66 days following permanent pouch emergence, and the mean ages at maturity for females and males was 341 and 466 days, respectively.

Reproduction in Sminthopsis-Longicaudata (Marsupialia, Dasyuridae) - Laboratory Observations

1986 ◽  
Vol 13 (1) ◽  
pp. 7 ◽  
Author(s):  
PA Woolley ◽  
A Valente
Keyword(s):  
Endangered Species ◽  
Breeding Season ◽  
Early Summer ◽  
Oestrous Cycle ◽  
Gestation Period ◽  
Late Winter ◽  
Breeding Condition ◽  
Males And Females ◽  
The Mean

Observations on the pattern of reproduction in Sminthopsis longicaudata, at present considered to be an endangered species, are presented. S. longicaudata is polyoestrous and in the laboratory females are in breeding condition from late winter (August) to early summer (December). They enter oestrus up to four times during the breeding season. Two litters were born 17 and 19 days post-mating, but the gestation period may be less than 15 days. The mean length of the oestrous cycle is 34.4 days. Both males and females may be able to breed in more than one season.

Breeding Biology of the Agile Wallaby, Macropus agilis (Gould) (Marsupialia : Macropodidae), in Captivity

1976 ◽  
Vol 3 (2) ◽  
pp. 93 ◽  
Author(s):  
JC Merchant
Keyword(s):  
Sexual Maturity ◽  
Post Partum ◽  
Cell Types ◽  
Morphological Characters ◽  
Oestrous Cycle ◽  
Vaginal Smear ◽  
Vaginal Smears ◽  
Main Cell ◽  
In Captivity ◽  
The Mean

Female agile wallabies in captivity reached sexual maturity at about 12 months old and males produced mature spermatozoa by 14 months. Breeding was continuous throughout the year and birth and oestrus were recorded in every month. The mean length of the oestrous cycle was 32.4 days, and the mean gestation period 29.4 days. Females exhibited post-partum oestrus, usually mating within 1 day of birth. Sixty-four young born in captivity comprised 24 males, 30 females and 10 of unknown sex. If a pouch young were removed or lost, the quiescent blastocyst resumed its development, to birth about 26.5 days later. Failure or absence of the blastocyst was followed by an oestrus at about the time of the corresponding post-partum oestrus. Both the oestrous cycle and the interval between removal of a pouch young and oestrus were significantly longer than when a pregnancy intervened. The oestrous cycle was characterized by changes in the proportions of the main cell types in the vaginal smear, and by changes in the appearance of the urogenital opening and the pouch and teats. The approach of oestrus could not be predicted from vaginal smears but the post-oestrous condition was always recognizable even without mating. Young animals first left the pouch for short periods between the ages of 176 and 211 days, and left permanently between 207 and 237 days. Animals of known age were measured and the development of various morphological characters noted at weekly intervals from about birth until 12 months old.

Studies of the oestrous cycle, oestrus and pregnancy in the koala (Phascolarctos cinereus)

Reproduction ◽  
2000 ◽  
pp. 49-57 ◽  
Author(s):  
SD Johnston ◽  
MR McGowan ◽  
P O'Callaghan ◽  
R Cox ◽  
V Nicolson
Keyword(s):  
Luteal Phase ◽  
Post Partum ◽  
Plasma Concentrations ◽  
External Genitalia ◽  
Oestrous Cycle ◽  
Phascolarctos Cinereus ◽  
Pregnant Females ◽  
Peripheral Plasma ◽  
The Mean ◽  
High Concentrations

As an integral part of the development of an artificial insemination programme in the captive koala, female reproductive physiology and behaviour were studied. The oestrous cycle in non-mated and mated koalas was characterized by means of behavioural oestrus, morphology of external genitalia and changes in the peripheral plasma concentrations of oestradiol and progestogen. The mean (+/- SEM) duration of the non-mated oestrous cycle and duration of oestrus in 12 koalas was 32.9 +/- 1.1 (n = 22) and 10.3 +/- 0.9 (n = 24) days, respectively. Although the commencement of oestrous behaviour was associated with increasing or high concentrations of oestradiol, there were no consistent changes in the morphology or appearance of the clitoris, pericloacal region, pouch or mammary teats that could be used to characterize the non-mated cycle. As progestogen concentrations remained at basal values throughout the interoestrous period, non-mated cycles were considered non-luteal and presumed anovulatory. After mating of the 12 koalas, six females gave birth with a mean (+/- SEM) gestation of 34.8 +/- 0.3 days, whereas the remaining six non-parturient females returned to oestrus 49.5 +/- 1. 0 days later. After mating, oestrous behaviour ceased and the progestogen profile showed a significant increase in both pregnant and non-parturient females, indicating that a luteal phase had been induced by the physical act of mating. Progestogen concentrations throughout the luteal phase of the pregnant females were significantly higher than those of non-parturient females. Parturition was associated with a decreasing concentration of progestogen, which was increased above that of basal concentrations until 7 days post partum.

Breeding Biology of Brushtail Possums Trichosurus vulpecula (Marsupialia, Phalangeridae) in Captivity.

1995 ◽  
Vol 18 (1) ◽  
pp. 1
Author(s):  
R.T. Gemmell
Keyword(s):  
Body Weight ◽  
Life Span ◽  
Post Partum ◽  
Young Female ◽  
Brushtail Possum ◽  
Lactation Period ◽  
In Captivity ◽  
In The Wild ◽  
The Mean ◽  
Reproductive Capability

The brushtail possum is a common arboreal marsupial that is well adapted to the Australian urban environment and to rearing in captivity. Data obtained from 100 female possums housed in a semi-captive colony over a 7 year period demonstrate the reproductive capability of this marsupial. The main breeding season is from March to June with a declining number of births occurring from July to October. The possums gave birth to 259 single young and one set of twins. The range of the lactation period was from 177 to 200 days with the birth of the subsequent young occurring at 188.4 ± 4.1 days post partum (SD, n = 5). The growth rate of the young female possum varied greatly after day 100 post partum, the mean body weight of possums at day 172, being 753.0 ± 76.2g (SD, n = 5) with a range of 685 to 851 g. Female possums, with a mean body weight of 2171 ± 388g, gave birth to their first litter on day 345.9 ± 69.3 days postpartum (mean, SD, n = 7). Although two female possums trapped in the wild were held in captivity for 64 and 63.4 months and one possum bred in captivity had a life span of 51.5 months, the mean life span was 21.0 ± 12.5 months (SD, n =3D 8), with a range of 14.3 to 51.5 months. This life span is very variable and it is of interest to determine if this is an artefact of captivity or is also observed in the wild.

Reproduction of the Red-Bellied Pademelon Thylogale billardierii (Marsupialia)

1982 ◽  
Vol 9 (1) ◽  
pp. 27 ◽  
Author(s):  
RW Rose ◽  
DJ McCatney
Keyword(s):  
Corpus Luteum ◽  
Post Partum ◽  
Oestrous Cycle ◽  
Seasonal Breeder ◽  
The Mean ◽  
Duration Of Gestation

'Thylogale billardierii, which is abundant in Tasmania, is a seasonal breeder with most births in the months April, May and June. Parturition is followed by mating, and the zygote so produced remains dormant until either sucking becomes intermittent near the end of pouch life or the young is lost. The mean length of the oestrous cycle was determined at 30.3 days, not significantly longer than the duration of gestation (30.2 days). Removal of pouch young results in the birth of a new young 28.7 days later. Removal of the corpus luteum results in oestrus 11 days later. Pouch life is 202 days, and vacation of the pouch by the young coincides precisely with parturition and post-partum mating. The young mature at about 14-15 months.

Movements and cumulative range size of the platypus (Ornithorhynchus anatinus) inferred from mark–recapture studies

2012 ◽  
Vol 60 (5) ◽  
pp. 352 ◽  
Author(s):  
M. Serena ◽  
G. A. Williams
Keyword(s):  
Range Size ◽  
River Catchment ◽  
Young Males ◽  
Adult Females ◽  
Ornithorhynchus Anatinus ◽  
Males And Females ◽  
The Mean ◽  
Western Victoria ◽  
Fyke Nets ◽  
Age And Sex

The extent of mammalian movements often varies with size, sex and/or reproductive status. Fyke nets were set along streams and rivers near Melbourne (southern Victoria) from the mid-1990s to 2007, and in the Wimmera River catchment (western Victoria) from 1997 to 2005, to assess how far platypus of different age and sex classes travelled between captures and over longer periods. The mean distance between consecutive captures of adults did not vary significantly as intervals increased from 1–3 months to >3 years, suggesting that most individuals occupied stable ranges. However, adult females travelled, on average, only 35% as far between captures as males in southern Victoria, and 29% as far in the Wimmera. Up to half of this difference may be explained by variation in size-related metabolic requirements. Immature males and females respectively moved 61% and 53% as far, on average, as their adult equivalents, although two young males dispersed >40 km. Adults incrementally occupied up to 13.9 km of channel in the case of a male (based on six captures over 67 months) and 4.4 km of channel in the case of a female (based on five captures over 127 months).

scholarly journals Effect of Sport Training and Education on Q Angle in Young Males and Females

2019 ◽  
Vol 7 (7) ◽  
pp. 17
Author(s):  
Orhan Ahmet Şener ◽  
Mehmet Durmaz
Keyword(s):  
Male Subject ◽  
Standing Position ◽  
Training And Education ◽  
Young Males ◽  
Sport Training ◽  
Undergraduate Study ◽  
Q Angle ◽  
Males And Females ◽  
The Mean ◽  
Male Subjects

The purpose of this study investigation of the effect of sport training and education on Q angle in young males and females. The Quadriceps Q angles of 240 female and 600 male subject were measured in both supine and standing positions by goniometer. It was used t-tests for statistical analyses. In this study, the average age was found to be 19.16 for women and 21.120 for men. The vast majority of participants are in the 17-22 age range. In this study, was found the mean Q angle of female and male subjects at supine position 15.710 and 13.020. On the other hand Q angle of female and male subjects at standing position were 17.050 and 14.040 respectively. The difference between mean Q angle of female and male subject was statistically significant (p<0.001). Between undergraduate study group and non-undergraduate group wasn't differences Standing Q angle and Supine Q angle statistically significant (p>0.05). Finally, the mean dominant knee Q angle of young females and males seemed to be in normal range. The high value of the knee Q angle of the dominant leg should be considered to be greater than 17 for males and 20 for females. The effect of physical activity on Q-angle should be investigated more extensively. It is thought that sport education has a decreasing effect on Q angle.

Sign in / Sign up

Export Citation Format

Share Document