Corrigendum to: Reproduction in the northern bettong, Bettongia tropica Wakefield (Marsupialia : Potoroidae), in captivity, with age estimation and development of the pouch young

2001 ◽  
Vol 28 (6) ◽  
pp. 647 ◽  
Author(s):  
Peter M. Johnson ◽  
Steven Delean

Reproduction in the northern bettong, Bettongia tropica, was studied in captivity. B. tropica is capable of breeding throughout the year, and mating behaviour is similar to that reported for other Bettongia species. The length of the oestrous cycle was 21–23 days, and the period of gestation was 20–23 days. Birth was usually followed by an oestrus and mating, and a subsequent lactation-controlled embryonic diapause. The interval between loss of pouch young and birth was 19–20 days. Permanent emergence from the pouch occurred at 102–112 days, and young at foot were weaned at 166–185 days of age. Linear mixed-effects models were used to describe polynomial growth equations for age determination of pouch young using both head and pes length. The relationship between error in age prediction and each body measurement was also defined. Pes measurements provided the most accurate estimates of the age of pouch young.

2001 ◽  
Vol 28 (1) ◽  
pp. 79 ◽  
Author(s):  
Peter M. Johnson ◽  
Steven Delean

Reproduction in the northern bettong, Bettongia tropica, was studied in captivity. B. tropica is capable of breeding throughout the year, and mating behaviour is similar to that reported for other Bettongia species. The length of the oestrous cycle was 21–23 days, and the period of gestation was 20–23 days. Birth was usually followed by an oestrus and mating, and a subsequent lactation-controlled embryonic diapause. The interval between loss of pouch young and birth was 19–20 days. Permanent emergence from the pouch occurred at 102–112 days, and young at foot were weaned at 166–185 days of age. Linear mixed-effects models were used to describe polynomial growth equations for age determination of pouch young using both head and pes length. The relationship between error in age prediction and each body measurement was also defined. Pes measurements provided the most accurate estimates of the age of pouch young.


2002 ◽  
Vol 29 (5) ◽  
pp. 463 ◽  
Author(s):  
Peter M. Johnson ◽  
Steven Delean

Reproduction of the purple-necked rock-wallaby, Petrogale purpureicollis, was studied in captivity. The length of the oestrous cycle was 36–38 days followed by a gestation period of 33–35 days. Birth was usually followed by an oestrus and mating, and a subsequent lactation-controlled embryonic diapause. The interval between loss of pouch young and birth was 30–36 days. Pouch life was 178–197 days and weaning occurred 92–171 days after permanent emergence from the pouch. The youngest age at which sexual maturity was reached was 21.8 months for males and 18 months for females. Linear mixed-effects models were used to describe polynomial growth equations for age determination of pouch young using both head and pes length. The relationship between error in age prediction and each body measurement was also defined. Head measurements provided the most accurate estimates of the age of pouch young.


1999 ◽  
Vol 26 (5) ◽  
pp. 631 ◽  
Author(s):  
Peter M. Johnson ◽  
J. Steven C. Delean

Reproduction in the Proserpine rock-wallaby, Petrogale persephone, was studied in captivity. Sexual maturity, defined as age at first fertility, was attained at 20.5 months in females whereas males were not mature until 24.8 months. P. persephone is capable of breeding throughout the year. The length of the oestrous cycle was 33–38 days, while the period of gestation was 30–34 days. Birth was usually followed by an oestrus and mating, and a subsequent lactation-controlled embryonic diapause. The mean interval between loss of a pouch young and birth was 31.5 days. Pouch life was 203–215 days and young at foot were weaned 105–139 days after permanent emergence from the pouch. Linear mixed-effects models were used to describe polynomial growth equations for age determination of pouch young using both head and pes length. The relationship between error in age prediction and each body measurement was defined. Head measurements provided the most accurate estimates of the age of pouch young.


2002 ◽  
Vol 24 (2) ◽  
pp. 193
Author(s):  
PM Johnson ◽  
S Delean

Macropus dorsalis was capable of breeding throughout the year. The period of gestation was 33 - 36 days. Birth was usually followed by an oestrus and mating, and a subsequent lactation-controlled embryonic diapause. The period between loss of pouch-young and birth was 29 - 30 days. Pouch life was 192 - 225 days and weaning occurred 81 - 159 days after permanent pouch emergence. Sexual maturity, defined as age at first fertility, occurred at 11.3 months in females and 15.7 months in males. Linear mixed-effects models were used to describe polynomial growth equations for age determination of pouch young using both head and pes length. The relationship between error in age prediction and each body measurement was also defined. Head measurements provided the most accurate estimates of the age of pouch young.


2003 ◽  
Vol 30 (5) ◽  
pp. 505 ◽  
Author(s):  
Peter M. Johnson ◽  
Steven Delean

Reproduction in Lumholtz's tree kangaroo, Dendrolagus lumholtzi, was studied in captivity. The length of the oestrous cycle was 47–64 days and the gestation period was 42–48 days. Post partum oestrus and embryonic diapause were not observed in this study. The interval between loss of a pouch young and a return mating was 22 days. Pouch life was 246–275 days long and weaning occurred 87–240 days later. Sexual maturity was obtained in females as early as 2.04 years and in males at 4.6 years. Linear mixed-effects models are used to describe polynomial growth equations for age determination of pouch young using both head and pes length. The relationship between error in age prediction and each body measurement is also defined. Head and pes measurements provide equally accurate estimates of the age of pouch young.


2021 ◽  
pp. 64-66
Author(s):  
Sambhunath Bandyopadhyay ◽  
Ritayan Sasmal ◽  
Debarshi Jana

Accurate gestational age determination is very important for management of continuation and termination planning of the pregnancy. rd To establish placental thickness as a parameter for determination of gestational age and fetal growth pattern at 3 trimester. 100 primigravida women who are fullling the inclusion criteria and attend gynae &obs OPD or admitted in their third trimester at IPGME&R from January 2017 to june 2018. Placental thickness at 3rd trimester USG scan is moderately correlated with gestational age, if placental thickness expressed in millimeter then it correlated with gestational age at weeks. rd st Placental thickness with >3.2 cm (32 mm) at 3 trimester almost associated with good fetal outcome, with APGAR score >8 at 1 min and birth weight >2500 gm.


1994 ◽  
Vol 21 (5) ◽  
pp. 553 ◽  
Author(s):  
PM Johnson ◽  
K Vernes

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.


1993 ◽  
Vol 20 (1) ◽  
pp. 97
Author(s):  
PM Johnson

Lagorchestes conspicillatus has a widespread distribution across northern Australia. Observations were made on reproduction in captive animals and a key produced for age determination of pouch young. Females commence breeding at about one year of age and males when slightly older. Reproduction in this species involved an oestrous cycle of 30 days, a gestation period of 29-31 days and a mean pouch life of 152 days. A postpartum oestrus and mating following a birth was the normal pattern of reproduction.


1973 ◽  
Vol 21 (3) ◽  
pp. 331 ◽  
Author(s):  
GM Maynes

Female M. parma in captivity reach sexual maturity at 11 1/2-16 months of age. Scrota1 size indicates that sexual maturity is attained in males at about 22 months. One male had spermatozoa at 19-20 months and another had a first fertile mating at 24-25 months. Mating behaviour is described and resembles that of other small macropodids. M. parma is monovular and polyoestrous. The oestrous cycle has a mean length of 4197810.72 days (n = 58; range 36-59 days) while the gestation period is 34.54*0.13 days (n = 28; range 33-36 days). Post-partum oestrus and mating occurred from 4 to 13 days after birth in a small proportion (16.7%) of those animals examined. However, most animals had an oestrus, while carrying a pouch young, between 45 and 105 days after birth. A few animals did not come into oestrus at all while carrying a pouch young. Removal of pouch young typically resulted in return to oestrus between 6 and 15 days later, in females that had not had a post-partum oestrus or an oestrus while carrying a pouch young. Females which mated at some stage during lactation prior to removal of pouch young gave birth 31.16 days later (n = 3; range 30.5-32.0 days). Three females at the Melbourne Zoo had estimated delayed gestation periods of 31, 31, and 32 days. The earliest observation of a young with its head out of the pouch was at 146 days of pouch life. Most young had left the pouch for short intervals by 175 days with the youngest observed out at 160 days. Young permanently leave the pouch at 211.9+-1.0 days (n = 10; range 207-218 days). Permanent exchange of pouch young has been observed in two cases, both at approximately the time young were first leaving the pouch for short intervals. Some females that mated while carrying a young in the pouch gave birth 6-11 days after permanent pouch exit of the primary young. Unmated females returned to oestrus 12-24 days after permanent pouch exit of their young. Young were weaned at 2 5 3 ) months after pouch exit. Most females entered anoestrus in 1968 following transfer of the animals into small holding pens. In 1969 only 5 of 24 matings resulted in young in the pouch, while in 1970 the corresponding figure was 21 of 44 matings. In both years there was evidence of young being born but apparently being lost during the climb from the urogenital opening to the pouch, probably because of overcrowding of the mothers. Evolution of embryonic diapause is discussed in relation to the reproductive pattern established for M. pavma. It is postulated that embryonic diapause first arose at the end of pouch life and has come to occupy the entire length of pouch life in most macropodids.


1989 ◽  
Vol 46 (4) ◽  
pp. 720-724 ◽  
Author(s):  
Didier Le Foll ◽  
Evelyne Brichet ◽  
Jean Louis Reyss ◽  
Claude Lalou ◽  
Daniel Latrouite

A method of age determination was developed on carapaces of the spider crab, Maja squinado Herbst and European lobster Homarus gammarus L., by measuring the natural radionuclides activity ratio, 228Th/228Ra in the exoskeleton. This method allows the determination of the time elapsed since the preceding molt of the animal. It was successfully tested on five spider crabs and four lobsters which had molted in captivity and therefore had a carapace of known age. It is probable that the method could, with some reservations, be extended to all marine Decapod Crustacea bearing a well calcified exoskeleton.


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