Reproductive behaviour before and after oestrus and oviposition in the captive short-beaked echidna (Tachyglossus aculeatus)
Kate J. Dutton-Regester A * , Alice Roser B , Haley Meer B , Marilyn B. Renfree C , Clive Phillips D E and Stephen D. Johnston AA School of Agriculture and Food Sciences, The University of Queensland, Gatton, Qld 4343, Australia.
B Currumbin Wildlife Sanctuary, Currumbin, Qld 4223, Australia.
C School of BioSciences, The University of Melbourne, Melbourne, Vic. 3010, Australia.
D Estonia University of Life Sciences, Institute of Veterinary Medicine and Animal Science, Tartu, Estonia.
E Curtin University Sustainability Policy Institute, Perth, WA, Australia.
Reproduction, Fertility and Development 34(14) 920-932 https://doi.org/10.1071/RD22092
Published online: 16 August 2022
© 2022 The Author(s) (or their employer(s)). Published by CSIRO Publishing. This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND)
Abstract
Context: Most of our current knowledge regarding echidna reproductive behaviour is based on qualitative measurements; therefore, it is unclear if specific behavioural cues could be utilised in their captive reproductive management.
Aims: This study aimed to identify quantitative changes in general and reproductive behaviour of echidna breeding pairs and pregnant females that might facilitate the detection of oestrus and impending oviposition and provide a summary of reproductive behaviour observed in a captive colony over a three-year observation period.
Methods: Three echidna breeding pairs and two trios were were monitored daily for seven reproductive and eight general behaviours during the 2020 breeding season. After confirmed copulation, females were monitored for four egg-laying and eight general behaviours until egg incubation. General observations of reproductive behaviours during the 2018–2020 breeding seasons were recorded as part of routine husbandry.
Key results: For breeding pairs, there was a significant rate of change over time before and after copulation for the behaviours ‘urogenital sniffing’, ‘rolling’ and ‘copulation attempt’. For pregnant females, time engaged in ‘pacing’ significantly increased while ‘time eating’ and the ‘qauntity of food eaten’ significanlty decreased on the day of oviposition. We were not able to identify oestrus from specific behaviours, but our observations suggest that the female echidna’s period of receptivity is less than 24 h.
Conclusions: The frequency that males express ‘urogenital sniffing’, ‘rolling’ and ‘copulation attempt’ toward the female can be used to alert zookeepers that copulation has likely occurred. Increased pacing, reduced feeding time and quantity of food eaten can aid zookeepers to identify impending oviposition.
Implications: This study demonstrates that there are quantifiable changes in specific echidna behaviours that can be incorporated into zoo husbandry practices to improve the reproductive management of this species.
Keywords: captive breeding, captive management, egg laying behaviour, oestrus detection, oviposition behaviour, reproductive behaviour, short-beaked echidna, Tachyglossidae.
References
Aplin K, Dickman C, Salas L, Helgen K (2016) Tachyglossus aculeatus. The IUCN Red List of Threatened Species 2016. Available at https://dx.doi.org/10.2305/IUCN.UK.2016-2.RLTS.T41312A21964662.enBeard, LA, and Grigg, GC (2000). Reproduction in the short-beaked echidna Tachyglossus aculeatus: field observations at an elevated site in South East Queensland. Proceedings of the Linnean Society of New South Wales 122, 89–99.
Blissitt, MJ, Bland, KP, and Cottrell, DF (1990). Discrimination between the odours of fresh oestrous and non-oestrous ewe urine by rams. Applied Animal Behaviour Science 25, 51–59.
| Discrimination between the odours of fresh oestrous and non-oestrous ewe urine by rams.Crossref | GoogleScholarGoogle Scholar |
Dutton-Regester, K, Keeley, T, Fenelon, JC, Roser, A, Meer, H, Hill, A, Pyne, M, Renfree, MB, and Johnston, S (2021). Plasma progesterone secretion during gestation of the captive short-beaked echidna. Reproduction 162, 267–275.
| Plasma progesterone secretion during gestation of the captive short-beaked echidna.Crossref | GoogleScholarGoogle Scholar |
Ferguson, A, and Turner, B (2013). Reproductive parameters and behaviour of captive short-beaked echidna (Tachyglossus aculeatus acanthion) at Perth Zoo. Australian Mammalogy 35, 84–92.
| Reproductive parameters and behaviour of captive short-beaked echidna (Tachyglossus aculeatus acanthion) at Perth Zoo.Crossref | GoogleScholarGoogle Scholar |
Gomez-Diaz, C, and Benton, R (2013). The joy of sex pheromones. EMBO reports 14, 874–883.
| The joy of sex pheromones.Crossref | GoogleScholarGoogle Scholar |
Griffiths M (1978) ‘The biology of monotremes.’ (Academic Press Inc: New York)
Guillette, LJ, Bjorndal, KA, Bolten, AB, Gross, TS, Palmer, BD, Witherington, BE, and Matter, JM (1991). Plasma estradiol-17β, progesterone, prostaglandin F, and prostaglandin E2 concentrations during natural oviposition in the loggerhead turtle (Caretta caretta). General and Comparative Endocrinology 82, 121–130.
| Plasma estradiol-17β, progesterone, prostaglandin F, and prostaglandin E2 concentrations during natural oviposition in the loggerhead turtle (Caretta caretta).Crossref | GoogleScholarGoogle Scholar |
Harris, RL, Holland, BR, Cameron, EZ, Davies, NW, and Nicol, SC (2014). Chemical signals in the echidna: differences between seasons, sexes, individuals and gland types. Journal of Zoology 293, 171–180.
| Chemical signals in the echidna: differences between seasons, sexes, individuals and gland types.Crossref | GoogleScholarGoogle Scholar |
Hurnik, JF, King, GJ, and Robertson, HA (1975). Estrous and related behaviour in postpartum Holstein cows. Applied Animal Ethology 2, 55–68.
| Estrous and related behaviour in postpartum Holstein cows.Crossref | GoogleScholarGoogle Scholar |
Hydbring, E, Madej, A, Macdonald, E, Drugge-boholm, G, Berglund, B, and Olsson, K (1999). Hormonal changes during parturition in heifers and goats are related to the phases and severity of labour. The Journal of Endocrinology 160, 75–85.
| Hormonal changes during parturition in heifers and goats are related to the phases and severity of labour.Crossref | GoogleScholarGoogle Scholar |
Jackson S (2003) ‘Australian mammals: biology and captive management.’ (CSIRO Publishing: Melbourne)
O’Brien, WF (1995). The role of prostaglandins in labor and delivery. Clinics in Perinatology 22, 973–984.
| The role of prostaglandins in labor and delivery.Crossref | GoogleScholarGoogle Scholar |
Perry, T, Toledo-Flores, D, Kang, WX, Ferguson, A, Laming, B, Tsend-Ayush, E, Lim, SL, and Grützner, F (2019). Non-invasive genetic sexing technique for analysis of short-beaked echidna (Tachyglossus aculeatus) populations. Reproduction, Fertility and Development 31, 1289–1295.
| Non-invasive genetic sexing technique for analysis of short-beaked echidna (Tachyglossus aculeatus) populations.Crossref | GoogleScholarGoogle Scholar |
Rismiller PD (1992) Field observations on Kangaroo Island echidnas (Tachyglossus aculeatus multiaculeatus) during the breeding season. In ‘Platypus and echidnas’. (Ed. ML Augee) pp. 101–105. (The Royal Zoological Society of New South Wales: Sydney)
Rismiller, PD, and McKelvey, MW (2000). Frequency of breeding and recruitment in the short-beaked echidna, Tachyglossus aculeatus. Journal of Mammalogy 81, 1–17.
| Frequency of breeding and recruitment in the short-beaked echidna, Tachyglossus aculeatus.Crossref | GoogleScholarGoogle Scholar |
Rismiller, PD, and Seymour, RS (1991). The echidna. Scientific American 264, 96–103.
| The echidna.Crossref | GoogleScholarGoogle Scholar |
Rørvang, MV, Nielsen, BL, Herskin, MS, and Jensen, MB (2018). Prepartum maternal behavior of domesticated cattle: a comparison with managed, feral, and wild ungulates. Frontiers in Veterinary Science 5, 45.
| Prepartum maternal behavior of domesticated cattle: a comparison with managed, feral, and wild ungulates.Crossref | GoogleScholarGoogle Scholar |
Swaisgood, RR, Lindburg, DG, and Zhang, H (2002). Discrimination of oestrous status in giant pandas (Ailuropoda melanoleuca) via chemical cues in urine. Journal of Zoology 257, 381–386.
| Discrimination of oestrous status in giant pandas (Ailuropoda melanoleuca) via chemical cues in urine.Crossref | GoogleScholarGoogle Scholar |
Takahashi, LK (1990). Hormonal regulation of sociosexual behavior in female mammals. Neuroscience & Biobehaviour Reviews 14, 403–413.
| Hormonal regulation of sociosexual behavior in female mammals.Crossref | GoogleScholarGoogle Scholar |
Wallage, A, Clarke, L, Thomas, L, Pyne, M, Beard, L, Ferguson, A, Lisle, A, and Johnston, S (2015). Advances in the captive breeding and reproductive biology of the short-beaked echidna (Tachyglossus aculeatus). Australian Journal of Zoology 63, 181–191.
| Advances in the captive breeding and reproductive biology of the short-beaked echidna (Tachyglossus aculeatus).Crossref | GoogleScholarGoogle Scholar |
Weiss, G (2000). Endocrinology of parturition. The Journal of Clinical Endocrinology & Metabolism 85, 4421–4425.
| Endocrinology of parturition.Crossref | GoogleScholarGoogle Scholar |
Ziegler, TE, Matteri, RL, and Wegner, FH (1993). Detection of urinary gonadotropins in callitrichid monkeys with a sensitive immunoassay based upan a unique monoclonal antibody. American Journal of Primatology 31, 181–188.
| Detection of urinary gonadotropins in callitrichid monkeys with a sensitive immunoassay based upan a unique monoclonal antibody.Crossref | GoogleScholarGoogle Scholar |