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Pen size and parity effects on maternal behaviour of Small-Tail Han sheep

Published online by Cambridge University Press:  10 April 2015

S.-J. Lv ,
Y. Yang ,
C. M Dwyer  and
F.-K. Li
S.-J. Lv*
Affiliation:
College of Life Sciences, Linyi University, Shuangling Road, Linyi City, 276005, Shandong, China
Y. Yang
Affiliation:
Linyi Agriculture Science Institute, North Street of Su River, Linyi City, 276009, Shandong, China
C. M Dwyer
Affiliation:
Animal & Veterinary Sciences, SRUC, King’s Buildings, West Mains Road, Edinburgh EH9 3JG, Scotland, UK
F.-K. Li
Affiliation:
College of Life Sciences, Linyi University, Shuangling Road, Linyi City, 276005, Shandong, China
*
†E-mail: [email protected]; [email protected]
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Abstract

The aim of this experiment was to study the effects of pen size and parity on maternal behaviour of twin-bearing Small-Tail Han ewes. A total of 24 ewes were allocated to a 2×2 design (six per pen), with parity (primiparous or multiparous) and pen size (large: 6.0×3.0 m; small: 6.0×1.5 m) as main effects at Linyi University, Shandong Province, China. Behaviour was observed from after parturition until weaning. All ewes were observed for 6 h every 5 days from 0700 to1000 h and from 1400 to 1700 h. Continuous focal animal sampling was used to quantify the duration of maternal behaviours: sucking, grooming and following as well as the frequency of udder accepting, udder refusing and low-pitched bleating. Oestradiol and cortisol concentrations in the faeces (collected in the morning every 5 days) were detected using EIA kits. All lambs were weighed 24 h after parturition and again at weaning at 35 days of age. The small pen size significantly reduced following (P<0.005), grooming (P<0.001) and suckling durations (P<0.05), as well as the frequency of udder refusals (P<0.001). However, there was a significant interaction with ewe parity, with decreased grooming and suckling in the small pen largely seen in the multiparous ewes (P<0.001). Independent of pen size, multiparous ewes accepted more sucking attempts by their lambs (P<0.05) and made more low-pitched bleats than primiparous ewes (P<0.001). Multiparous ewes had higher faecal oestradiol concentrations than primiparous ewes (P<0.001), and ewes in small pens had higher faecal cortisol levels compared with ewes in larger pens (P<0.001). As lambs increased in age, the duration of maternal grooming, following and suckling as well as frequency of udder acceptance and low-pitched bleating all declined, and the frequency of udder refusing increased (P<0.001 for all). Ewe parity, but not pen size, affected lamb weight gain during the period of observation (P<0.001). This is the first study to show that pen size, interacting with parity, can affect the expression of maternal behaviour in sheep during lactation. The study is also the first to report on the maternal behaviour of Chinese native sheep breeds (Small-Tail Han sheep), with implications for the production of sheep in China.

Keywords

pen sizeparitySmall-Tail Han sheepmaternal behaviourcortisol
Type
Research Article
Information
animal , Volume 9 , Issue 7 , July 2015 , pp. 1195 - 1202
Copyright
© The Animal Consortium 2015 

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References

Alexander, G, Stevens, D, Kilgour, R, de Langen, H, Mottershead, BE and Lynch, JJ 1983. Separation of ewes from twin lambs: incidence in several sheep breeds. Applied Animal Ethology 10, 301–317.Google Scholar
Averòs, X, Lorea, A, Beltrán de Heredia, I, Ruiz, R, Marchewka, J, Arranz, J and Estevez, I 2014a. The behaviour of gestating dairy ewes and different space allowance. Applied Animal Behaviour Science 150, 17–26.Google Scholar
Averòs, X, Lorea, A, de Heredia, IB, Arranz, J, Ruiz, R and Estevez, I 2014b. Space availability in confined sheep during pregnancy, effects in movement patterns and use of space. PLoS One 9, e94767.Google Scholar
Bahr, NI, Pryce, CR, Dobeli, M and Martin, RD 1998. Evidence from urinary cortisol that maternal behavior is related to stress in gorillas. Physiology & Behavior 64, 429–437.Google Scholar
Bøe, KE, Berg, S and Andersen, IL 2006. Resting behaviour and displacements in ewes – effects of reduced lying space and pen shape. Applied Animal Behaviour Science 98, 249–259.Google Scholar
Bosing, BM, Susenbeth, A, Hao, J, Ahnert, S, Ohm, M and Dickhoefer, U 2014. Effect of concentrate supplementation on herbage intake and live weight gain of sheep grazing a semi-arid grassland steppe of North-Eastern Asia in response to different grazing management systems and intensities. Livestock Science 165, 157–166.Google Scholar
Caroprese, M, Casamassima, D, Rassu, SPG, Napolitano, F and Sevi, A 2009. Monitoring the on farm welfare of sheep and goats. Italia Journal of Animal Science 8, 343–354.Google Scholar
Chang, H, Liu, XL and Geng, SM 1998. Studies on animal genetic resources in China. Shaanxi People’s Education Press, Xi’an, China. (in Chinese).Google Scholar
Chiumenti, R 1987. Costruzioni rurali. Edagricole, Bologna, Italy.Google Scholar
Dwyer, CM 2008. Genetic and physiological effects on maternal behavior and lamb survival. Journal of Animal Science 86, E246–E258.CrossRefGoogle Scholar
Dwyer, CM 2014. Maternal behaviour and lamb survival: from neuroendocrinology to practical application. Animal 1, 102–112.Google Scholar
Dwyer, CM and Lawrence, AB 1998. Variability in the in expression of maternal behaviour in primiparous sheep: effects of genotype and litter size. Applied Animal Behaviour Science 58, 311–330.Google Scholar
Dwyer, CM and Smith, LA 2008. Parity effects on maternal behaviour are not related to circulating oestradiol concentrations in two breeds of sheep. Physiology and Behaviour 93, 148–154.Google Scholar
Dwyer, CM, Gilbert, CL and Lawrence, AB 2004. Pre-partum plasma oestradiol and post-partum cortisol, but not oxytocin, are associated with individual differences in maternal behaviour in sheep. Hormones and Behaviour 46, 529–543.Google Scholar
Dwyer, CM, McLean, KA, Deans, LA, Chirnside, J, Calvert, SK and Lawrence, AB 1998. Vocalisations between mother and young in sheep: effects of breed and maternal experience. Applied Animal Behaviour Science 58, 105–119.Google Scholar
Gonyou, HW and Stookey, JM 1985. Behavior of parturient ewes in group-lambing pens with and without cubicles. Applied Animal Behaviour Science 14, 163–171.Google Scholar
Heiming, RS, Bodden, C, Jansen, F, Lewejohann, L, Kaiser, S, Lesch, KP, Palme, R and Sachser, N 2011. Living in a dangerous world decreases maternal care: a study in serotonin transporter knockout mice. Hormones and Behavior 60, 397–407.Google Scholar
Hild, S, Coulon, M, Schroeer, A, Andersen, IL and Zanella, AJ 2011. Gentle vs aversive handling of pregnant ewes: I. Maternal cortisol and behavior. Physiology and Behaviour 104, 384–391.Google Scholar
Horton, GMJ, Malinowski, K, Burgher, CC and Palatini, DD 1991. The effects of space allowance and sex on blood catecholamines and cortisol, feed consumption and average daily gain in growing lambs. Applied Animal Behaviour Science 32, 197–204.Google Scholar
Le Neindre, P, Poindron, P and Delouis, C 1979. Hormonal induction of maternal behaviour in non-pregnant ewes. Physiology and Behaviour 22, 731–734.Google Scholar
McNatty, KP, Cashmore, M and Young, A 1972. Diurnal variation in plasma cortisol levels in sheep. Journal of Endocrinology 54, 361–362.Google Scholar
Meurisse, M, Gonzalez, A, Delsol, G, Caba, D, Levy, F and Poindron, P 2005. Oestradiol receptor-alpha expression in hypothalamic and limbic regions of ewes is influenced by physiological state and maternal experience. Hormone and Behaviour 48, 34–43.Google Scholar
Möstl, E and Palme, R 2002. Hormones as indicators of stress. Domestic Animal endocrinology 23, 67–74.Google Scholar
Nowak, R, Porter, RH, Levy, F, Orgeur, P and Schaal, B 2000. Role of mother–young interactions in the survival of offspring in domestic mammals. Review Reproduction 5, 153–163.Google Scholar
Palme, R and Möstl, E 1997. Measurement of cortisol metabolites in faeces of sheep as a parameter of cortisol concentration in blood. International Journal of Mammal Biology 62 (suppl. 2), 192–197.Google Scholar
Pickup, HE and Dwyer, CM 2011. Breed differences in the expression of maternal care at parturition persist throughout the lactation period in sheep. Applied Animal Behaviour Science 131, 8–14.Google Scholar
Poindron, P, Le Neindre, P, Lévy, F and Keverne, EB 1984. Les mécanismes physiologiques de l’acceptation du nouveau-néchez la brebis. Biology Behaviour 9, 65–88.Google Scholar
Sevi, A, Casamassima, D, Pulina, G and Pazzona, A 2009. Factor of welfare reduction in dairy sheep and goat. Italian Journal of Animal Science 8 (suppl. 1), 81–101.Google Scholar
Sevi, A, Massa, S, Annicchiarico, G, Dell'Aquila, S and Muscio, A 1999. Effect of stocking density on ewes’ milk yield, udder health and microenvironment. Journal of Dairy Research 66, 489–499.Google Scholar
Sevi, A, Taibi, L, Albenzio, M, Muscio, A and Dell’Aquila, S 2000. Effect of parity on milk yield, composition, somatic cell count, renneting parameters and bacteria counts of Comisana ewes. Small Ruminate Research 37, 99–107.Google Scholar
Shillito-Walser, E, Walters, E and Ellison, J 1984. Observations on vocalization of ewes and lambs in the field. Behaviour 91, 190–203.Google Scholar
Val-Laillet, D and Nowak, R 2006. Socio-spatial criteria are important for the establishment of maternal preference in lambs. Applied Animal Behaviour Science 96, 269–280.Google Scholar
Winfield, CG 1970. The effect of stocking intensity at lambing on lamb survival and ewe and lamb behaviour. Proceedings of the Australian Society of Animal Production 8, 291–296.Google Scholar