Behaviour and neonatal survival

Imminent parturition triggers a decreased social affiliation in the ewe who seeks a suitable place to give birth (see reviews; Dwyer and Lawrence, Reference Dwyer and Lawrence2005; and Supplementary Material). Birth-site selection will determine the micro-environment in which the lamb will be born, and can potentially influence the success of lamb thermoregulatory responses (see below) if ewes select sheltered and protected birth sites. Wet, windy and cold weather are important factors in deaths of lambs from hypothermia (Alexander et al., Reference Alexander, Lynch, Mottershead and Donnelly1980). In addition, time spent at the birth site is an important factor in preventing separation between ewes and lambs, thus selection of a birth site with features that will encourage the ewe to remain at the site for a prolonged period can also influence survival.

Maternal behaviour of parturient ewes and goats is very similar (Poindron et al., Reference Poindron, Levy and Keller2007). During and immediately after birth ewes and goats are very attracted to the smell and taste of amniotic fluids, and will lick fluids that have been spilt during the birth process, transferring this attraction to the newborn. Maternal behaviour in the first few hours after delivery consists of focussed licking and grooming of the young, accompanied by frequent low-pitched bleats, and acceptance of the neonate at the udder. Licking or grooming serves to dry the offspring, and is important in the formation of an exclusive olfactory memory in the mother for her own neonates. This is established within an hour or so of giving birth, and the dam will then restrict her maternal care only to those offspring with which she has formed an exclusive attachment. Failure to develop this attachment will result in the mother not recognising the lamb or kid as her own and rejecting attempts by the neonate to access the udder and suck. As other lactating females will also reject the lamb or kid, these newborns will not survive without human intervention. Following olfactory recognition, mothers then learn to identify their lamb or kid via their visual appearance at a distance, and then by their vocalisations (Poindron et al., Reference Poindron, Levy and Keller2007).

Maternal behaviour by the ewe can facilitate lamb-sucking responses, by standing and making the udder more available to the teat-seeking lamb. Inexperienced ewes are less likely to cooperate with lamb-sucking attempts, initially, which may contribute to the reduced survival of the lambs of primiparous ewes. However, ewe behaviour alone cannot induce the lamb to suck, and separation of ewe and lamb behavioural effects by embryo transfer (Dwyer and Lawrence, Reference Dwyer and Lawrence1999), suggests that maternal behaviour does not encourage greater vigour and vitality in her newborn lamb. Maternal attachment scores have a negligible correlation with lamb survival (Hatcher et al., Reference Hatcher, Eppleston, Thornberry and Watt2010) and measures of maternal behaviour are also poorly genetically correlated with lamb survival (Brien et al., Reference Brien, Cloete, Fogarty, Greeff, Hebart, Hiendleder, Hocking Edwards, Kelly, Kind, Kleeman, Plush and Miller2014), suggesting that variation in the quantity or quality of maternal behaviour expressed may not have a great influence on lamb survival.

In contrast, lamb behaviour is crucial in determining survival. At birth, lambs move through a series of behavioural events directed towards standing, udder seeking and sucking. Standing reduces heat loss to the ground, so helping the lamb to maintain body temperature, and the lamb then employs a series of reflex and coordinated responses to move along the body of the ewe and locate the udder. The speed with which the lamb accomplishes these behaviours is known to be related to its probability of survival (Dwyer et al., Reference Dwyer, Lawrence, Bishop and Lewis2003). Moreover, lambs that derive from sires or lines of sheep with good survival are quicker to stand and suck than lambs from high loss lines or sires (Cloete and Scholtz, Reference Cloete and Scholtz1998; Hergenhan et al., Reference Hergenhan, Hinch and Ferguson2014). Suckling quickly provides the lamb with nutrients, particularly to sustain thermoregulation, and immunoglobulins to provide passive immunity. In addition, suckling and ingestion of colostrum play a role in the development of attachment of the lamb for its mother (Goursaud and Nowak, Reference Goursaud and Nowak1999).

Lamb and kid behaviour is affected by many of the same risk factors that are associated with increased mortality. Behavioural development is impaired in lambs that have been delivered after a prolonged labour, in larger litters and in male lambs compared with female (Dwyer, Reference Dwyer2003). Furthermore, lamb birthweight exhibits a U-shaped distribution with lamb vigour at birth in a similar way to lamb survival (Dwyer et al., Reference Dwyer, Lawrence, Bishop and Lewis2003). Breed, line and sire within breed variation in lamb behaviour has been demonstrated in many studies (Cloete and Scholtz, Reference Cloete and Scholtz1998; Hergenhan et al., Reference Hergenhan, Hinch and Ferguson2014; and see Supplementary Materials). The early vigour or sucking ability of lambs has been shown to have a moderate heritability (Matheson et al., Reference Matheson, Bünger and Dwyer2012), suggesting that improving lamb vigour may be possible by genetic selection, which would lead to improved survival. Whether similar genetic relationships and phenotypic associations with survival exist for goat kid behaviour is not known.

Physiology and neonatal survival

At birth, ambient temperatures can drop from 39°C in utero to 10°C or lower. Maintenance of body temperature depends on the balance between heat loss and heat production. Heat loss is mainly affected by body surface area (small lambs have a higher surface area/BW ratio than large lambs, thus they lose heat faster and are more at risk of hypothermia) and the insulation value of the coat (short, fine birth coats have lower insulation value than long, coarse coats). A wet coat, by amniotic fluid, reduces insulation value but removal of the fluid by maternal licking or grooming contributes to the lamb’s ability to maintain normal body temperature. Within 10 min of birth the lamb increases heat production but important inter-individual variations are observed (Dwyer and Morgan, Reference Dwyer and Morgan2006), and in the most extreme cases, where lambs are unable to generate sufficient heat, hypothermia is irreversible. Heat production comes from two main mechanisms in the neonate: non-shivering thermogenesis, mostly if not all attributable to brown adipose tissue, and shivering thermogenesis, which usually takes place under cold conditions, mainly in older, dry lambs, and metabolises muscle glycogen. Details of the thermogenic mechanisms employed by neonatal small ruminants are given in the Supplementary Material.

Colostrum contains nutrients, immunoglobulins and other elements such as enzymes, hormones, growth factors and neuroendocrine peptides. Colostrum contains fat (7% to 13%), non-immunoglobulin protein (4% to 10%) and lactose (2% to 5%), and provides 6 to 7 kJ of energy/ml (Nowak and Poindron, Reference Nowak and Poindron2006; Banchero et al., Reference Banchero, Milton, Lindsay, Martin and Quintans2015). At 18°C to 26°C, lambs require 50 ml colostrum/kg within the first 18 h of life to make up for lipid energy deficit and prevent hypothermia, at 0°C to 10°C requirements increase to 280 ml colostrum/kg. Early ingestion of colostrum has an additional benefit in that it increases heat production by 17% even if body energy reserves are still replete, enhancing resistance to hypothermia. Under optimal conditions, neonates would consume sufficient colostrum to meet their carbohydrate requirement for 14 h of the first 24 h of life (Mellor and Cockburn, Reference Mellor and Cockburn1986). Utilisation of glycogen is therefore essential to make up the difference, and lambs face the first few days with largely depleted liver and muscle glycogen. Colostrum yield is dependant on adequate supplies of both energy and protein in the last 3 weeks of gestation. Although twin-bearing ewes generally yield more colostrum than single-bearing ewes, their onset of lactation is slower and they do not produce as much colostrum per lamb (Banchero et al., Reference Banchero, Milton, Lindsay, Martin and Quintans2015). Thus, multiple-born lambs, compared with singles, are disadvantaged, in addition to lower birthweights and energy reserves, and higher surface area/BW ratios. Inadequate nutrition during gestation can delay the onset of lactogenesis, reduce colostrum and milk production, and affect colostrum viscosity (Banchero et al., Reference Banchero, Milton, Lindsay, Martin and Quintans2015). As a consequence, delayed suckling may lead to energy reserves being exhausted within 6 h of birth and result in depressed heat production. Insufficient intake of colostrum is the second major factor affecting neonatal survival after body reserve depletion.

Late pregnancy is associated with a considerable rise in cortisol concentration in the lamb in the last 24 to 48 h, as activation of the hypothalamic–pituitary–adrenal function triggers the birth process (Challis and Brooks, Reference Challis and Brooks1989). This results in high circulating cortisol, which may be responsible for vigorous locomotor activity and teat-seeking behaviour, as vaginal birth and concomitant stress hormones are associated with increased neonatal arousal (Lagercrantz and Slotkin, Reference Lagercrantz and Slotkin1986). High plasma cortisol in lambs in the first postnatal hours prevents premature gut closure and therefore may enhance macromolecule absorption (Hough et al., Reference Hough, McCarthy, Thatcher, Kent and Eversole1990). The decline in cortisol concentration observed in the following days coincides with periods during which thyroid hormones increase as thermal efficiency improves and rectal temperature stabilises. The perinatal rise of cortisol is accompanied by an increase in triiodothyronine and thyroxine, which is maintained throughout early postnatal life. Thyroid hormones are known to play an important role in regulating oxygen consumption; failure to maintain high plasma triiodothyronine concentration results in a decrease in oxygen consumption, hypothermia and death (Symonds et al., Reference Symonds, Bird, Clarke, Gate and Lomax1995). However, the relationship of cortisol with survival is complex: alongside the beneficial effects of elevated neonatal cortisol, excessively high levels at birth may be related to difficult parturition and fatal dystocia, whereas an increase in circulating cortisol in the following days reflect a state of chronic stress owing to inadequate milk supply and is associated with elevated blood glucose to compensate for lack of nutrient intake (Chniter et al., unpublished).

Improved lamb viability beyond 72 h is associated with decreased vulnerability to chilling, singleton status, higher pre-suckling body temperature, decreased pre-suckling glucose concentrations, high plasma concentration of proteins, lipids and immunoglobulins, and a moderate rise in neonatal cortisol concentration (Eales et al., Reference Eales, Murray and Small1982; Miller et al., Reference Miller, Blache, Jackson, Downie and Roche2010). Being bigger is an advantage in terms of vigour and thermoregulation, as lambs are more efficient in their suckling activity and in resisting cold exposure. However, birthweight can be affected by breed (Slee, Reference Slee1981; Dwyer and Morgan, Reference Dwyer and Morgan2006), season of birth (Chniter et al., Reference Chniter, Hammadi, Khorchani, Ben Sassi, Ben Hamouda and Nowak2013), variation within a litter or prenatal nutrition.

Immune function and neonatal survival

The ruminant placenta is epitheliochorial and does not allow the transfer of immune components from the mother to the young. Newborn lambs and kids are thus born markedly hypogammaglobulinaemic, and depend entirely on passive transfer of colostral immunoglobulins, acquired by suckling, for immunological protection after birth. Passive immunity must be acquired within a very narrow time window as, in newborn lambs, gut closure to immunoglobulin absorption occurs between 24 and 36 h after birth (Hough et al., Reference Hough, McCarthy, Thatcher, Kent and Eversole1990). However, colostral immunoglobulins also decline rapidly in the hours after birth, to virtually zero within 24 h of birth (Al Sabbagh et al., Reference Al Sabbagh, Swanson and Thompson1995), so early suckling is a prerequisite for effective transfer. Lamb mortality is associated with low immunoglobulin status 24 h after birth (Kenyon et al., Reference Kenyon, Stafford, Morel and Morris2005), demonstrating the importance of ensuring good colostrum intake in newborn small ruminants.

Adequate colostrum intake relies on two complementary factors: the ability of the lamb to ingest sufficient amounts (through vigorous sucking behaviour) and the concentration and quantities of colostral immunoglobulins available from the ewe. Partitioning the sources of variation in lamb serum immunoglobulin on farm suggests that 56% of the variation can be attributed to the lamb (e.g. volume ingested), 36% to the ewe and only 7% to the farm (Christley et al., Reference Christley, Morgan, Parkin and French2003). Correlation between ewe colostral immunoglobulin concentrations and lamb serum immunoglobulin concentrations is generally low (McGuire et al., Reference McGuire, Regnier, Kellom and Gates1983), suggesting that other factors are important in ensuring good immunological protection for the offspring. Ensuring adequate sucking behaviour from the newborn, and cooperation from the dam, are therefore crucial to achieve adequate immunological protection. However, improving maternal immunoglobulin supply would also be beneficial. On farm data suggests that 22% of ewes produced <50 g/l immunoglobulin G at lambing, which is considered inadequate to meet the needs of a lamb owing to its ingestion capacity. The considerable between-animal variation in the amount of IgG available in colostrum is affected by dam age (younger ewes produced more immunoglobulin), litter size, udder health, season of lambing in tropical regions and late gestational nutrition (Gilbert et al., Reference Gilbert, Gaskins, Hillers, Parker and McGuire1988; and see Supplementary Material). There is some evidence for genetic factors influencing maternal colostrum immunoglobulin content with sire and breed effects reported, and a heritability of 0.19 for ewe immunoglobulin concentration in colostrum (Gilbert et al., Reference Gilbert, Gaskins, Hillers, Parker and McGuire1988).

Nutritional factors influencing neonatal survival

Adequate nutrition of the ewe or goat during pregnancy is essential to produce viable offspring, which can thrive in the postnatal environment. Extensive research (see recent reviews for individual studies; Kenyon and Blair, Reference Kenyon and Blair2014; Rooke et al., Reference Rooke, Arnott, Dwyer and Rutherford2015) has described how changes in nutrition, both total and specific nutrient supply, impact on neonatal lamb characteristics relevant to survival. As, in temperate regions, the ewe is a seasonal breeder, and pregnancy in these climatic zones coincides with winter when nutrient availability from grazing is limited, an annual cycle approach to feeding the ewe has long been advised (Russell, Reference Russell1985; Figure 3). Lactation, the period of maximum nutrient demand, normally occurs in spring when pasture growth and quality are at a maximum. After weaning lambs in mid/late summer, the ewe is able to replenish body reserves mobilised during gestation and lactation. Subsequently, deficits in feed nutrient supply, primarily energy, during gestation are balanced by mobilisation of adipose tissue. Thus, undernutrition (UN) is the nutrient imbalance most commonly encountered by the pregnant ewe. This imbalance is also seen in pregnant goats although, in tropical regions, this results from the annual cycle of rain and dry rather than day length as in temperate zones.

Figure 3 Illustration of the optimal changes in ewe weight (as a proportion of her weight at mating) during the reproductive cycle. Values given on the curve are indicative average body condition scores.

Maternal UN can influence neonatal lamb mortality in several ways. Directly, UN may reduce lamb birthweight and thereby increase mortality risk. Maternal UN can also adversely affect lamb neonatal behaviour and the ability of the lamb to thermoregulate. UN also influences mothering ability of the ewe, hence the establishment of the ewe–lamb bond (Dwyer et al., Reference Dwyer, Lawrence, Bishop and Lewis2003), and the amount and quality of colostrum produced by the ewe. Similarly in goats, UN in the last third of gestation is associated with altered maternal care and impaired recognition abilities of mothers. However, the extent to which UN influences mortality through each of these routes has not been thoroughly investigated. Rooke et al. (Reference Rooke, Arnott, Dwyer and Rutherford2015) found, across all studies reviewed, that UN consistently reduced birthweight only in the last third of ovine pregnancy with the reduction in birthweight being related both to the length and severity of UN. In the first two-thirds of pregnancy, UN only reduced birthweight in specific circumstances. These included severity of UN: feeding only 0.15 of requirement between gestation days 0 and 60 reduced birthweight and increased mortality. Breeds more adapted to adverse conditions (e.g. Scottish Blackface) partitioned more nutrients to the foetus and thereby maintained birthweight in response to early gestational UN challenge, whereas birthweight was reduced in breeds selected for more rapid growth (e.g. Suffolk). Ewes in good body condition were better able to withstand the challenge of UN than ewes in poorer body condition. Decreased birthweight, however, is only a risk factor for increased lamb mortality. Where both lamb birthweight and mortality were recorded (Rooke et al., Reference Rooke, Arnott, Dwyer and Rutherford2015), in only half the studies was a decrease in birthweight accompanied by increased mortality. Contributory factors will be how large the decrease in birthweight was, the physical environment and the amount and quality of husbandry. Importantly, feeding the ewe nutrients in excess of requirements for foetal growth and ewe maintenance was not associated with improvements in lamb survival; in fact negative outcomes were more common than positive ones. This is supported by studies that show a U-shaped relationship between lamb birthweight and survival (Figure 4).

Figure 4 Relationship between lamb mortality rate (proportional mortality) and birthweight (in kg) for Scottish Blackface lambs, demonstrating the optimal birthweight, for this breed, lies between 3 and 5 kg.

In relation to specific nutrients, most research has focussed on trace elements and vitamins where deficiency is a practical problem, and linked to increased mortality (e.g. deficiencies of copper, cobalt or iodine). Interpretation of many studies is difficult because the baseline status of ewes (deficient, marginal or adequate) before the study is frequently not well defined. Where the status of ewes was marginal, supplementation improved survival, or associated measures, for cobalt, selenium and vitamin E (reviewed by Rooke et al., Reference Rooke, Dwyer and Ashworth2008). Responses where pre-experiment ewe status was adequate have been more equivocal and there is little evidence for any benefits to supplying trace nutrients in excess of requirement but short of toxicity (Rooke et al., Reference Rooke, Dwyer and Ashworth2008).

In summary, providing there are no chronic deficiencies in trace element and vitamin supply, UN is the main nutritional risk to neonatal lamb survival, particularly in the last trimester. As long as ewes have adequate body reserves at mating (Figure 3), loss of body condition over the first 100 days of pregnancy does not impose a markedly increased risk of lamb mortality. Where ewes are housed in late pregnancy, loss of body condition can be avoided by adequate feeding. Ewes kept outside on pasture are probably more at risk either from chronic UN from lack of grass growth or acute UN from adverse weather, for example, snowfall.

Genetic aspects of neonatal survival

Selecting for improved lamb survival both reduces ‘wastage’ while improving animal welfare, whereas selection for higher litter size inevitably increases lamb losses as lambs from multiple births have higher risk of mortality. Considering lamb survival ‘as a trait of the lamb’ in the context of a multi-trait breeding index, is predicted to improve lamb survival at a faster rate than if it is considered as being a ‘trait of the ewe’ (Conington et al., Reference Conington, Bishop and Simm2002).

The heritability of lamb survival is generally low with most published estimates being <0.1 (e.g. Safari et al., Reference Safari, Atkins, Fogarty and Gilmour2005; Brien et al., Reference Brien, Cloete, Fogarty, Greeff, Hebart, Hiendleder, Hocking Edwards, Kelly, Kind, Kleeman, Plush and Miller2014; and see Supplementary Material), although higher heritability estimates in experimental flocks have been documented (e.g. 0.13 to 0.33; Sawalha et al., 2007). Low heritability can in part be explained because farmers often do not record lambs born dead; and because the multifactorial nature of lamb mortality may mean that genetic variation in different causes of mortality may differ. Moreover, where flocks have a high degree of human intervention, lambs that would otherwise have died are often kept alive, thus the degree of human intervention may be an additional variable. It seems logical that extensively managed flocks, with low or no human intervention at the time of lambing, rely greatly on the expression of ewe and lamb behaviours that contribute to higher rates of survival. For these systems, the definition of the breeding goal can be relatively straightforward. Recent analyses (for details see Supplementary Material) for Scottish Blackface sheep estimate heritability for survival at 0.05 and 0.09, with lamb birthweight being the most important predictor of survival.

The use of ‘component’ traits for lamb survival such as aspects of lamb vigour and ability to reach critical ‘survival milestones’ (e.g. sucking) have been suggested (Matheson et al., Reference Matheson, Bünger and Dwyer2012). For farmers who are keen to reduce reliance on human intervention around lambing time and to identify families of more vigorous lambs, using such ‘indicators’ of propensity to have higher survival makes good sense. Unfortunately, the time required to implement some of the measures is prohibitive and so alternatives to behavioural observational milestones are preferable.

It is likely that the molecular basis to lamb survival is highly polygenic, that is, many different gene variants are involved in the complex biological mechanisms associated with survival. Some key mechanisms, such as ability to generate heat through non-shivering thermogenesis, have been described above and the genetic basis to cold resistance documented (also see Supplementary Material). There is evidence that a variant of the ovine β3-adrenergic receptor gene (ADRB3) is associated with higher risk of cold-related mortality in Merino sheep in New Zealand (Forrest et al., Reference Forrest, Hickford, Wynyard, Merrick, Hogan and Frampton2006). However, when extended to 13 other NZ breeds and crosses, the frequency of that gene variant was low or non-existent, suggesting that it may already have been selected against in the breeds tested. It also highlights the inherent risks associated with translating results of gene associations found for one breed to all genotypes. Gene discovery for specific components of lamb survival will continue although the application of genomic breeding values: integrating single nucleotide polymorphism data with good survival phenotypes with lamb birthweight is perhaps more realistic.

Practical applications

Can the scientific knowledge outlined above lead to practical solutions to lamb mortality? The critical role of birthweight as a risk factor for neonatal mortality has been emphasised throughout: lamb vigour, udder-seeking and thermoregulatory ability are impaired in low birthweight lambs, and heavy lambs are vulnerable to dystocia and birth injury. Thus, ensuring an optimal intermediate birthweight (within breed), rather than maximising birthweight, is a key goal to increase survival. This requires attention to detail in feeding ewes, some mechanism for checking that nutrition is optimal (such as regular body condition scoring or assessing circulating β-hydroxybutyrate), and use of ultrasound scanning to determine litter size to tailor nutritional strategies appropriately. However, the interacting factors of litter size and ewe age still make this difficult to achieve practically. Defining the intermediate weight as a breeding goal will also help to ensure neonatal birthweights are targeted correctly.

Neonatal hypothermia is a significant cause of lamb mortality in many environments. Although heat loss and heat production can be influenced by birthweight, lambs can also be protected by provision of shelter, particularly those that are born outdoors, to limit the impact of evaporative heat loss. Research has investigated the impact of type and placement of different shelters in lambing paddocks (Pollard, Reference Pollard2006; and see Supplementary Material), but the factors determining birth-site selection by ewes, and thus the likelihood of births occurring in shelter, has not received much attention. Familiarity with the terrain, such as may be achieved with set stocking, influences shelter use, which suggests that permanent structures, or temporary features that are introduced well before lambing, may increase their use. Providing a sufficient number of appropriate birth sites for flock size is also important to prevent contamination of preferred sites, and to minimise the likelihood of mismothering if maternal ewes are forced to lamb in close contact with one another.

An adequate intake of colostrum is a fundamental component of lamb survival. Many of the risk factors for lamb mortality (Figure 2) have their root in preventing or reducing the uptake of sufficient colostrum by the lamb. Although the biological impact of sucking colostrum on neonatal responses has not been fully elucidated, ensuring that neonatal ruminants gain access to the udder and ingest colostrum as soon as possible after birth is probably the single most important factor in their subsequent survival. Although some newborns may require the provision of supplementary colostrum, it is preferable for neonates to find the udder of their mother and suck themselves, if this can be achieved within a reasonable timescale (ideally within 2 h of birth). Lambs tube-fed colostrum are less active and are licked less frequently by their mothers in comparison with naturally suckled lambs (Garcia Gonzalez and Goddard, Reference Garcia Gonzalez and Goddard1998), which may indicate disrupted bonding.

Although the genetic component to lamb survival may be small, or difficult to measure accurately, there is opportunity to improve lamb survival by genetic means. In addition, appreciation that birth difficulty can impair lamb behaviour and survival, and thus selecting sires on the basis of lambing ease, should also improve lamb survival.

On farm data collection

In France, a participative study generated detailed on farm knowledge from ‘real farm’ situations and disseminated best practice. Data were collected on farms using one of three different farming systems: one lambing period per year, pastoral system and accelerated system (three lambing in 2 years) to understand factors associated with lamb mortality (for details see Supplementary Material). Overall mortality was 13.4%, but varied across farms from 3.6% to 31.2%. Lamb mortality followed a similar pattern to experimental studies, with 54% of mortality occurring within the first 2 days of life. However, the farmers in the study felt that they had little or no ability to influence lamb mortality during this period, and had more control over mortality occurring after the first 2 days. The main causes of mortality were very small lambs or sucking problems, although a large number of mortalities were of unknown cause.

Farms were very variable in the distribution of risk factors for lamb mortality. However, the main risk factors regularly observed were: ewes lambing with low body condition scores and deficient selenium status (as defined by selenium concentration of <60 μg/l in at least three ewes), impaired colostrum intake, poor hygiene in the lambing sheds and mixed flocks with lambs of different ages.

Flock and management factors

Intensive lamb rearing is associated with increased mortality (Binns et al., Reference Binns, Cox, Rizvi and Green2002), although deaths from stillbirths are reduced. For indoor flocks, lamb mortality rates are lower where there is continuous monitoring (Holmøy et al., Reference Holmøy, Kielland, Stubsjøen, Hektoen and Waage2012). Likewise, mortality is higher in larger flocks (>900 lambing ewes; Binns et al., Reference Binns, Cox, Rizvi and Green2002). These authors suggest that the increased risk may not be related to flock size per se, but to the reduced supervision ewes in larger flocks might receive. The presence of a stockperson allows prompt assistance with cases of dystocia and reduces deaths associated with difficult births.

Active involvement to ensure sufficient colostrum intake improves lamb survival. However, flocks where tube feeding is routine had increased neonatal mortality compared with flocks where assistance with suckling was the routine intervention (Holmøy et al., Reference Holmøy, Kielland, Stubsjøen, Hektoen and Waage2012). These differences may be associated with the increased risk of infection with tube feeding, or the role of sucking in behavioural interactions as described above. Use of tube feeding may also be more frequent in flocks where neonatal mortality rates already are high.

Lambs managed indoors may be exposed to high pathogen burdens in the environment, especially during peak lambing. Providing new bedding for lambing pens daily influenced mortality rates in the first 24 h after birth, but not subsequently (Binns et al., Reference Binns, Cox, Rizvi and Green2002). Treating sick lambs with electrolytes was associated with low perinatal mortality rates, whereas fostering of lambs increased the risk (Binns et al., Reference Binns, Cox, Rizvi and Green2002). Fostering of lambs may be an indicator of a large proportion of multiple births in the flock, and thus the underlying reason for the increased risk observed. However, housing factors do not appear to be related to neonatal mortality, indicating that management practices should be the main focus when preventive flock level factors are addressed.

Taken together the participative study and epidemiological analyses suggest that on farm lamb mortality occurs for similar reasons as shown in the experimental work, and that similar risk factors are relevant. It should be emphasised that the studies described were predominantly in ewes housed at lambing time. Some of the practices described above as important determinants of lamb mortality rates may not be practical in other outdoor production systems.

Knowledge exchange

Farmers acquire knowledge from many sources: written resources, farmer-focussed events, discussion groups and one-to-one interactions with advisors or veterinarians (Dodunski, Reference Dodunski2014). Farmers consistently rate face-to-face interactions as their preferred means of acquiring knowledge (Ingram, Reference Ingram2008), and prefer activities involving practical and hands-on means of teaching (Dodunski, Reference Dodunski2014). In a study of advisor–farmer interactions, Ingram (Reference Ingram2008) characterised different types of knowledge exchange events and concluded that facilitative encounters, where the advisor and farmer worked together to address the situation, sharing their knowledge and experience, were the most effective in providing farmer education and development. This suggests that advisors or veterinarians are an important source of knowledge for farmers to improve lamb or kid survival, but the nature of this exchange can have an impact on the uptake and use of the information.

Decisions regarding management change

As research suggests that management practices are of greater importance than housing, improvements in neonatal lamb survival rates depend on changes in the farmers’ decisions and behaviour. Many approaches to understanding decision making assume that the decision maker is only focussed on maximising profit, which may in fact not always be the case. Farmers, particularly on small farms, tend to value the way of life, independence and performance above expressive, social and instrumental aspects such as a high income (Gasson, Reference Gasson1973; Muri et al., personal communication).

The Theory of Planned Behaviour (Ajzen, Reference Ajzen1991) suggests that the immediate antecedent of behaviour is behavioural intention, which is under the influence of attitudes, subjective norms and perceived behavioural control. Attitude is the degree to which people evaluate something with favour or disfavour – in this case lamb mortality rates and the specific management procedures that may reduce them. Subjective norms are a person’s perception of the extent to which important referents (e.g. other farmers, family members) would approve or disapprove of particular actions. Perceived behavioural control is a measure of the extent to which people believe they are able to control the outcome, for example, whether they actually think they can reduce lamb mortality through the suggested management change. In this regard, the results from the French participative study, which suggested that farmers felt they had little control over perinatal lamb mortality, are particularly interesting. Using this theory in a qualitative approach, Australian sheep farmers were shown to have a positive attitude to improving lamb survival rates, but differed in their beliefs about how to achieve this (Elliott et al., Reference Elliott, Sneddon, Lee and Blache2011). Social norms and perceived behavioural control played a significant role in decision making, and other farmers appear to be the most important referents. Furthermore, external factors such as type of farm, sheep breed, etc., also played an important role, as well as the characteristics of the farmers themselves (Elliot et al., Reference Elliott, Sneddon, Lee and Blache2011).

These data suggest that effective knowledge transfer of the increasing body of scientific research would be best achieved by one-to-one encounters, using a facilitative approach to explore the specific farm risk factors and derive workable farm-level solutions. This can help overcome factors, such as the apparent perception of lack of control over early lamb mortality, and may also be useful to challenge the perceived norms around neonatal mortality. The within-farm variation in mortality, which is observed in all studies that have gathered these data, provides evidence from commercial farms, rather than experimental studies, of what can be achieved. The process of improving on farm mortality may also be aided by collection of more specific data on farm, such as actual rather than estimated mortality rates and causes. Where this has been achieved, the rather pessimistic picture provided in the literature, that mortality rates have remained unchanged over the past 40 years can begin to be challenged.

Success stories

An example of successful facilitative knowledge exchange, conducted largely as small-scale discussion groups with a group of motivated farmers in the United Kingdom, has begun to deliver considerable benefits in terms of knowledge exchange and improvements in lamb mortality. Relevant to the discussions above about subjective norms are farmers that have chosen to move away from maximising lambing percentages (which might be viewed by other farmers as evidence of success but accompanied by higher losses) to achieve similar numbers of lambs weaned through a lower lambing percentage and lower mortalities. This more sustainable outcome might provide greater job satisfaction, without necessarily impacting on farm profitability.

Other successful examples include the uptake of behavioural and experimental information on the importance of lamb behaviour and its genetic components. Although these have not been used to derive breeding values for animals, improvements in lamb survival have been reported by culling or not re-breeding animals that have required assistance at lambing, where lambs required assistance to suck or where ewes have abandoned lambs. Similar strategies involve only selecting well-grown lambs from a group that produced and reared twins, thus selection is based on ability to rear two lambs rather than for litter size.

On farm nutritional strategies that minimise the seasonal variation in ewe body condition have also been employed. Often these have not been prescriptive nutritional regimes, but are based on improved knowledge about the issues and costs to ewe and lamb survival of poor gestational nutrition, and then a workable solution derived that meets the needs of the individual farm to optimise the nutritional management of the flock. The advisor’s role may have been to help the farmer to make decisions about behavioural change, as outlined above, to prioritise nutrition, and then helping to develop a solution that can be achieved on the farm.

Evidence for an improvement in lamb survival in these situations may often be anecdotal, or reported in trade papers, and may not have been published in scientific journals. However, farmers either culling or moving to different breeds are reporting improved shelter seeking by ewes (of wool-shedding breeds), improved lamb thermoregulatory ability, and improved maternal care leading to better lamb survival.