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Stracke, J., & Berger, A. (2012). Project on paternal effects to the cognitive and social development of the offspring on feral horses (Equus caballus). In K. Krueger, & (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Horses provide an interesting animal model to test short- and long-term effects of the paternal influence on the offspring under natural conditions. As a highly social animal, horse naturally is living in long-term harem groups building strong familiar bonds. Arguing that the environment of a juvenile is highly important for the development of cognitive and social functions as well as for the emotional competence, a future study on domestic horses wants to highlight the paternal influence on the offspring as well as special effects of the stallion during the first two years of the foals´ life. Nowadays, in most husbandry systems it is still common to keep the stallions separated, raising the offspring in an intact harem group is very rare. The aim of this study is to describe the role of the stallion in the early development of the foal in an extensive pasture management system living in natural harem groups. Results are going to be compared to findings of studies on groups without the male present in the rearing phase. A precise behavioural analysis is planned; direct behavioural observations are going to be supported by long-term and continuously activity measures by special telemetry collar systems. Additional physiological measures should give evidence of the investment of the stallion. The young horses will be confronted with different tests of cognitive and social abilities (exploration behaviour, fear behaviour, play behaviour). The results of this study will contribute to fundamental research in the behaviour of the horse and might display an important step to animal welfare in modern horse husbandry. It will be possible to set a time-frame in which the male does have positive influence on the offspring and therefore should be kept with the family. A detailed knowledge of the influence of the male to cognitive and social abilities could as well be applicable in the training of horses and therefore be of great importance in equestrian sports.
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Dalla Costa, E., Rabolini, A., Scelsa, A., Canali, E., & Minero, M. (2012). A study on inter-observer reliability of castration pain assessment in horses. In K. Krueger, & (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Pain evaluation is a key issue for equine welfare and it is often cause of concern because it is difficult to determine its intensity and duration. This is essential when different people are looking after the animals and they need to decide when or not giving analgesics to guarantee the welfare of the subject. The most widely used technique to determine pain in horses is identifying pain related behaviors. The aim of this study was to determine inter-observer reliability of two different assessors evaluating pain related behaviors in horses undergoing castration. 8 stallions of different breed, aged between 2 and 4 years, were included in the study. All the subjects underwent routine castration (closed technique in general anesthesia). The subjects were placed in an observation box for 5 days and their behavior was recorded for 15 minutes before the surgery and 4, 8, 16, 24 and 40 hours after intervention. Two blind observers, using a given ethogram of horse pain related behaviors modified from literature (for a review Ashley, 2005), analyzed horses behavior at each interval. Descriptive statistics and K Kendall test were performed. Observers agreed significantly assessing agitation, reluctance to move, kicking the abdomen, lethargy, rolling, attention and curiosity (P<0.05), however agreement was low for head movements, stretching, flank watching, lowered head carriage, weight shifting, abnormal movement, fixed stare. Our results show that assessing pain in horses should be a cause of concern, because different pain related behaviors are difficult to identify and to have agreement between two observers. Training of care takers of horses on identification of specific behaviors is needed to standardize pain assessment. Acknowledgements: The authors wish to thank the EU VII Framework programme (FP7-KBBE-2010-4) for financing the Animal Welfare Indicators (AWIN) project and for providing funds for Emanuela Dalla Costa and Michela Minero to present this paper.
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Ermilina, J. A. (2012). Dominance hierarchy in feral horses in Rostov Region. In K. Krueger, & (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Horses maintain the social structure through the establishment of dominant-subordinate hierarchical relationships, both within and between groups. The object of study was the feral horse population, living on the Vodnyi Isl, Manych-Ghudilo Lake, on the territory of Rostov Region, S Russia the State Nature Biosphere Reserve “Rostov”. The social structure of this population is represented by the harem and bachelor groups, and their variety – the “mixed”groups, the presence and composition of which is atypical for the populations of feral horses. The main objectives of this work were to identify the hierarchical structure of different types of social groups and the role of the stallions in them, defining the dominance rank of animals. The method of continuous logging occurred aggressive reaction, ritualized interaction between stallions, take into account the direction of interactions between individuals. We observed 5 harem, 3 bachelor and 3 mixed groups. Each group was studied for a total of 60 h (8 h per group per days).Behavioral observations were carried out in summer 2009-2011. Based on the number and direction of aggressive interactions the hierarchical coefficient was calculated for individual horses (Ivanov et al, 2007). Harem group consists of an adult stallion (<5 years old) and a few mares with their offspring. Our observations of harem groups confirm the previously known information about this type of social groups (Berger, 1986; Carson, Wood-Gush, 1983, Keiper, 1983). Hierarchical system between mares is close to linear with reversal. The stallion is not included in the hierarchy of the mares; he is the leader and serves to maintain the integrity of the group and inter-group hierarchy, and has reproductive function. Bachelor groups consist of stallions 2-3 years and older who do not have their own harem. It is known that dominance hierarchy in these groups is linear, young males or males who recently had joined the group have low ranks (Berger, 1977; Houpt, Keiper, 1982; Kirillov Paklina, 1990). In observed bachelor groups dominant stallion have a significantly higher rank in the hierarchy. However, among other stallions is not always observed strict linear hierarchy – some individuals have very similar ranks. Function of managing the group and maintaining the intergroup hierarchy can be distributed among the all stallions in the group. Mixed groups are composed of several mature stallions, one or more mares (sometimes with the offspring). In the study population in this type of social groups animals may be mature (age 5 and older) and semi-mature (2-5 years). The hierarchy of these atypical groups has not been studied. In the studied 3 mixed groups stallions have very similar hierarchical rank, dominant and subordinate stallions share a function of managing the group, participation in ritualized interactions. Our studies have revealed the plasticity of the hierarchical structure of groups of horses and the need to further investigate the distribution of social roles among stallions.
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Flauger, B., & Krueger, K. (2012). Social feeding decisions in horses (Equus caballus). In Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Like many other herbivores equids feed on rather evenly distributed resources. Especially in ruminants several studies have proved the influence of social organisations, rank, sex and the depletion of feeding sites on the feeding behaviour of individuals. However, it is not yet understood whether social aspects affect horses´ feeding decisions. Horses roam on vast habitats with constantly changing vegetation. In non-competitive situations domestic horses tend to return to the same feeding site until it is overgrazed. Whereas, for competition over limited food the social status of the individuals appears to be important. Curiosity about the influence of social rank and different social feeding conditions on the horses´ feeding decisions between two buckets, equally filled with high-quality surplus food, led us to create the test situation described here. The observer horses were alternately tested with a dominant and a subordinate demonstrator placed in one of three different positions. We conclude that domestic horses use cognitive strategic decision making in order to decide where to feed in a social feeding situation. When possible they tend to return to the same, continuously supplied feeding site and switch to an “avoidance tendency” when another horse is already feeding from it or in the presence of a dominant horse. Thus the position and the social rank of conspecifics affect the feeding strategy of horses.
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Bouskila, A., de Vries, H., Hermans, Z. M., & van Dierendonck, M. (2012). Leadership roles in movements of free-roaming Konik horses (Equus caballus) in a Dutch reserve. In K. Krueger, & (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: We observed the activity and movements of Konik horses (Equus caballus) in order to determine the initiators of movements and the individuals taking the lead in movements of the main groups. We conducted our observations between March-June 2010 along the shores of the Rhine river, in the Blauwe Kamer reserve, in the Netherlands. The horses were introduced to the reserve alongside with cattle to prevent the growth of the forest and maintain the grass habitat. We videotaped all observations on two digital video cameras, one providing the general view of the group and the other scanning and focusing on the individuals, to aid with identification. Horses were recognized based on individual profiles that were created for each one, consisting of photos of both sides and notes of the main characters, such as orientation and coloration of the mane, prominent scars and markings, etc. Twenty three horses (not counting foals) were organized in two harem groups with 11 individuals (two of which were dominant stallions) in the large group and six individuals (one of which was a stallion) in the second group. These two main groups were always within sight of each other, and two bachelor males moved usually in their vicinity. An additional group of three young bachelor males roamed elsewhere in the reserve. We divided the movements of the horses to local movements while grazing and to long-distance movements, in which the horses moved to a different grazing location, to a pond of water, resting area or groups of trees that were used by the horses for scratching themselves. During the local movements, any two of the three oldest females in the large harem group were enough to cause the whole group to follow them and gradually change position within the pasture. The smaller harem always followed the large harem’s movements. The long-distance movements of the large harem were sometimes initiated by one of the harem stallions that herded their group and at other times – by the oldest females. Soon after the movement was clearly initiated, the dominant stallions positioned themselves in the back of the group or in the center and had no influence on the direction of move that was only determined by the leading females. In the long-distance movements too, the small harem followed the large harem group, and the two bachelor males usually followed behind them. Social interactions included aggressive interactions between the two dominant males within the large harem or between dominant stallions and the two bachelor males accompanying the two harems. In addition, dominant males courting or attempting to mate with mares sometimes caused a turmoil that eventually initiated movement of the harems. KW -
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Szarka, A., Nagy, K., & Maros, K. (2012). Approaching a horse, approaching a human: Tolerating and seeking human contact in pastured horses. In K. Krueger, & (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: We tested untrained horses (foals and breeding mares) in 3 different breeding centres. Horses were kept in a pasture during daytime in bigger groups (median 12, min: 6, max 35 / pasture) according to age, gender and breed (hungarian halfbred, hucul, arabian and thoroughbred). To measure their reactions to an unfamiliar person we conducted an active and a passive human test. In the active human test the test person (TP) approached a focal animal in the group from a predetermined direction: from their front, from their side (left or right) or from the rear. As TP reached the horse (of app. 0.5 m distance), she tried to pet the animal’s head. The TP always chose and approached a standing or a grazing horse (ie. those that were not walking, galloping, playing etc.). The horse’s reaction to the approaching human was scored 1-5. Score 1: the horse moved away and the TP could not even approach it within 0.5 m; Score 2: the horse made max. 2 steps away, but could be reached and petted; Score 3 and Score 4: the horse stood in its place but showed different signs of discomfort (head turn – Score 3; backing ears, tail slash – Score 4); Score 5: the horse stood and did not show any sign of discomfort or actively approached the TP. There was no significant difference in the horses’ reaction between approaching from their left or right side. Approaching from their front or from their side (left or right) did not differ significantly either. However, the odds of walking away from the TP (score 1 or 2) was 2.7 (Fisher-test, p=0.039) and 3.3 (p=0.012) times higher when TP approached from the rear compared to approaching from their front or from their side (left or right), respectively. In the passive human test the TP stood immobile for 4 minutes in 5 or 10 m far from the horses during their active (grazing) or inactive (standing idle during noon) period. Horses approached TP significantly sooner (general linear model, p=0.017) when she stood 5m distance (38 ±63 s) compared to 10m (97 ±52 s). The arrival of a second horse after the first horse approached the TP showed significant high correlation with the latency of the first horse arrival (Pearson correlation, r=0.96, p<0.001). The horses were less keen (p=0.008) to approach the human when they were tested in an inactive period (177 ±110 s) compare to active period (38 ±63 s).
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Warmuth, V., Eriksson, A., Bower, M. A., Barker, G., Barrett, E., Hanks, B. K., et al. (2012). Reconstructing the origin and spread of horse domestication in the Eurasian steppe. Proc Natl Acad Sci U S A, .
Abstract: Despite decades of research across multiple disciplines, the early history of horse domestication remains poorly understood. On the basis of current evidence from archaeology, mitochondrial DNA, and Y-chromosomal sequencing, a number of different domestication scenarios have been proposed, ranging from the spread of domestic horses out of a restricted primary area of domestication to the domestication of numerous distinct wild horse populations. In this paper, we reconstruct both the population genetic structure of the extinct wild progenitor of domestic horses, Equus ferus, and the origin and spread of horse domestication in the Eurasian steppes by fitting a spatially explicit stepping-stone model to genotype data from >300 horses sampled across northern Eurasia. We find strong evidence for an expansion of E. ferus out of eastern Eurasia about 160 kya, likely reflecting the colonization of Eurasia by this species. Our best-fitting scenario further suggests that horse domestication originated in the western part of the Eurasian steppe and that domestic herds were repeatedly restocked with local wild horses as they spread out of this area. By showing that horse domestication was initiated in the western Eurasian steppe and that the spread of domestic herds across Eurasia involved extensive introgression from the wild, the scenario of horse domestication proposed here unites evidence from archaeology, mitochondrial DNA, and Y-chromosomal DNA.
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Krueger, T. (2012). Rinder- und Pferdebeweidung ist gut für die Natur. Junge Wissenscahften, 93, 28–35.
Abstract: Rinder und Pferde werden in den Abruzzen das ganze Jahr auf großen Weiden gehalten. Dies fördert nachweislich den Artenreichtum, verbessert die Bodenqualität und trägt durch Kohlenstoffbindung zum Klimaschutz bei.
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Schneider, A. - C., Melis, A. P., & Tomasello, M. (2012). How chimpanzees solve collective action problems. Proceedings of the Royal Society B: Biological Sciences, .
Abstract: We presented small groups of chimpanzees with two collective action situations, in which action was necessary for reward but there was a disincentive for individuals to act owing to the possibility of free-riding on the efforts of others. We found that in simpler scenarios (experiment 1) in which group size was small, there was a positive relationship between rank and action with more dominant individuals volunteering to act more often, particularly when the reward was less dispersed. Social tolerance also seemed to mediate action whereby higher tolerance levels within a group resulted in individuals of lower ranks sometimes acting and appropriating more of the reward. In more complex scenarios, when group size was larger and cooperation was necessary (experiment 2), overcoming the problem was more challenging. There was highly significant variability in the action rates of different individuals as well as between dyads, suggesting success was more greatly influenced by the individual personalities and personal relationships present in the group.
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Baumgartner M. (2012). Liegeverhalten von Pferden im Offenlaufstall auf unterschiedlichen Bodenmaterialien (Gummimatten, Späne und Sand) [Recumbency patterns of horses stabled in group housing systems on different bedding materials (rubber mats, shavings and sand)]. Ph.D. thesis, , Munich.
Abstract: Die angemessenste Art ein Pferd als soziales Wesen unter menschlicher Obhut zu halten, ist in der Gruppe mit Seinesgleichen. Dabei gilt der Offenlaufstall mit getrennten Funktionsbereichen (Mehrraum-Außenlaufstall mit Auslauf) als die tiergerechteste Haltungsform für Pferde (BMELV, 2009). Aus Gründen der Arbeits- und Kostenersparnis sowie zur Reduzierung der Keim- und Staubbelastung werden in jüngster Zeit vermehrt Gummimatten als Einstreuersatz in Liegehallen von Offenlaufställen eingesetzt.
In vorliegender Arbeit sollte überprüft werden, ob Gummimatten (7,5 cm hoch, schaumstoffgefüllt; HIT-Softbed plus®) in Kombination mit minimaler Späneeinstreu als Liegeunterlage in Liegehallen von Offenlaufställen als tiergerecht beurteilt werden können. Darüber hinaus galt es zu klären, ob die Klimaverhältnisse in den Liegehallen trotz nicht saugfähiger Gummiunterlage den hygienischen Anforderungen des BMELVs (2009) an das Stallklima entsprechen. Dazu wurde das Liegeverhalten von einer repräsentativen Anzahl von 56 Pferden in einem Offenlaufstall mit getrennten Funktionsbereichen an jeweils 6 Tagen je Jahreszeit (Frühling, Sommer, Herbst, Winter) mittels kontinuierlicher Videoaufzeichnungen (n= 24 Tage) und zusätzlichen visuellen Direkt-beobachtungen (n= 60 Std) erfasst. Die Pferde hatten zum Liegen die Wahl zwischen folgenden drei Arealen: drei identisch ausgestatteten, jedoch unterschiedlich großen Liegehallen (mittig Gummimatten; Randbereich Späneeinstreu), einem Unterstand (Sand), sowie einem Sandplatz. Die Größe der Liegefläche in den drei Liegehallen (LH I 172 m², LH II und III jeweils 143 m²) entsprach den Anforderungen des BMELVs (2009). Unterstand und Sandplatz konnten zusätzlich von den Pferden zum Ruhen im Liegen genutzt werden. Ergänzend wurden folgende Einflussfaktoren auf das Liegeverhalten der Pferde erfasst: Tageszeit, Jahreszeit und Witterung sowie Alter, Stockmaß, Gewicht, „Body Condition Score“ und Rangordnung.
Durchschnittlich ruhten lediglich 35,2 der 52,3 in der Anlage befindlichen Pferde (67,3%) pro Beobachtungstag im Liegen in den Arealen. Demzufolge nahmen
Zusammenfassung 213
viele Pferde nicht jede Nacht eine Liegeposition ein. Die Hauptliegezeit mit 72% der erfassten Liegephasen war zwischen 0 und 6 Uhr. Bezogen auf die vorhandene Liegefläche je Areal ergab sich lediglich eine 50%ige Maximalauslastung an gleichzeitig liegenden Pferden.
Die Liegephasendauer variierte -unabhängig vom Areal- signifikant zwischen den Pferden (p=0,028) und darüber hinaus auch je Pferd (p<0,001). Die durchschnittliche Dauer pro Liegephase war mit 28,8 ± 0,5 (SEM) min signifikant länger in den Liegehallen (I, II und III), als im Unterstand mit 24,6 ± 0,9 min und auf dem Sandplatz mit 20,0 ± 1,9 min (p<0,001).
Die mittlere tägliche Gesamtliegedauer eines Pferdes betrug 91 ± 2,7 min in den Liegehallen (I, II und III), 43 ± 2,3 min im Unterstand und 27 ± 2,9 min auf dem Sandplatz (p<0,001). In den Liegehallen legte sich ein Pferd im Mittel 3,2 Mal am Tag ab, im Unterstand lediglich 1,7 und auf dem Sandplatz 1,3 Mal (p<0,001). 79% der registrierten Liegephasen (n= 2410) fanden darüber hinaus in den Liegehallen (I, II und III) statt, was deren zentrale Bedeutung als Liegebereich hervorhebt.
In der größeren Liegehalle I ruhten eine größere Anzahl an unterschiedlichen Pferden häufiger (p<0,0002) und länger (p<0,0005) pro Tag im Liegen als in den beiden etwas kleineren Liegehallen II und III.
Die tägliche Gesamtliegedauer pro Pferd war mit aufgestütztem Kopf mit 54,8 ± 1,6 Minuten länger als ohne aufgestützten Kopf mit 45,2 ± 1,8 min. In Seitenlage wurde im Durchschnitt pro Tag und Pferd 27,5 ± 1,1 min geruht (p<0,001). Diese Ruheposition wurde in den Liegehallen signifikant häufiger eingenommen, als auf dem Sandplatz oder im Unterstand (p<0,001).
Die tägliche mittlere Gesamtliegedauer pro Pferd auf Späne war mit 74,3 ± 2,9 min gegenüber 62,4 ± 2,3 min auf Gummimatten signifikant länger (p=0,005). Ebenso fanden in Relation zum Flächenangebot in den Liegehallen geringfügig mehr Liegephasen auf dem Späne-Bereich als auf den Gummimatten statt. Ebenfalls in Flächenrelation wurde der offen gestaltete Unterstand deutlich vor den anderen Arealen zum Ruhen im Liegen von den Pferden präferiert. Es sei deshalb auf die Bedeutung eines Unterstandes als zusätzliche Liegefläche in Offenlaufstallhaltung hingewiesen.
Die meisten Liegephasen und auch die längsten täglichen Liegezeiten fanden in den warmen Monaten statt (p=0,013). Im Winter flachte das Ruhen im Liegen
deutlich ab und verlagerte sich bei unter -10°C nahezu ausschließlich auf die Liegehallen (p=0,001).
Der leichte Späne-Überzug und der positive Effekt der bereits integrierten und die Gummimatten zum Liegen nutzenden Pferde waren mögliche Gründe dafür, dass die Neuankömmlinge ohne Gummimatten-Vorerfahrung (n= 10 Pferde ≤ 6 Monate in der Anlage) kein vermindertes Liegeverhalten im Vergleich zur bestehenden Herde (n= 46 Pferde; mind. 1 bis max. 3 J. in der Anlage) aufwiesen.
Die Rangordnung wurde mittels modifiziertem „Average Dominance Index“ berechnet. Die rangniederen Pferde hatten mit 2,6 gegenüber 3,4 und 3,1 sowohl signifikant weniger Liegephasen pro Pferd und Tag, als auch mit 69,3 ± 3,9 min eine um 22 min signifikant kürzere tägliche Gesamtliegedauer als die Ranghöheren (jeweils p<0,001). Rangniedrige Pferde ruhten in den Liegehallen weniger häufig (2,7 gegenüber 3,5 und 3,2 mittlere Anzahl Liegephasen/ Pferd/ Tag) und auch signifikant (p<0,001) kürzer je Tag (77,8 ± 5,0 min gegenüber 97,3 ± 3,9 min und 98,8 ± 5,1 min). Je jünger ein Pferd war, desto öfter (3,5 gegenüber 2,6 mittlere Anzahl Liegephasen/ Pferd/ Tag) und länger (103,7 ± 7,6 min gegenüber 56,1 ± 13,2 min) legte es sich am Tag nieder, und desto häufiger (90% der Liegephasen der 4 und 5 Jährigen gegenüber 39% und 70% der 16 bis 25 J.) nutzte es die Liegehallen zum Liegen (p<0,001). Das Stockmaß der Pferde und das Pferdegewicht zeigten keinen eindeutigen Einfluss auf das Liegeverhalten. Für den „Body Condition Score“ (Skala 1 bis 9) ergaben sich signifikante Unterschiede. Je höher der BCS der Pferde war, desto häufigere (p=0,0185) und längere Liegezeiten (p=0,007) wiesen sie auf.
Der monatlich gemessenen Ammoniakgehalt sowie Luftgeschwindigkeit, Luftfeuchtigkeit und Temperatur entsprachen bei Einsatz von Gummimatten in den Liegehallen den Anforderungen des BMELV (2009) an ein tiergerechtes Stallklima. Voraussetzung hierfür ist jedoch eine ausreichende Luftzirkulation im Stallgebäude sowie eine gute Stallhygiene.
Die Ergebnisse aus den vergleichenden Beobachtungen der unterschiedlichen Liegematerialien lassen schlussfolgern, dass die hier untersuchten verformbaren Gummimatten in Kombination mit minimaler Späneeinstreu in Offenlaufställen von der Mehrzahl der Pferde zum Ruhen im Liegen angenommen wurde und deshalb als weitgehend tiergerecht beurteilt werden können.
[Being highly social animals, horses are housed most adequately in groups. Loose housing systems are said to be the most species adequate system of horse housing (BMELV, 2009). Recently rubber mats have increasingly been used instead of shavings as bedding in loose housing systems where the different functional areas are separated. Advantages of rubber mats are that they are less cost and labour intensive as shavings, and their use also reduces the bacterial and dust contamination of the environment.
However, it has not yet been shown whether horses are capable of satisfying their recumbency needs on rubber mats as well as they can on shavings. This study looks to clarify this question, as well as to evaluate the hygienic conditions of the stabling climate in the areas equipped with sponge-filled rubber mats (HIT-Softbed® plus).
The recumbency patterns of 56 horses kept in a loose housing system with separate functional areas were observed on 6 days per season (spring, summer, autumn and winter) using wide angle video cameras. The different areas were: three similar but different large halls meant as lying areas (in the middle rubber mats; in the periphery shavings), an unsheltered area with sand footing and a sheltered area with sand footing. The size of the three halls meant as lying areas (LH I 172 m², LH II and III each 143 m²) was adequate with the demands of the BMELV (2009). Confounding factors which could also affect recumbency behaviour, such as day time, season and weather were taken into account. The role of the horses rank was also investigated. The occurrence of disruptions during recumbency phases by other members of the herd was also found out. Horse specific factors such as age, height, weight and body condition score were also taken into account as these could also have an effect on recumbency patterns.
On each day of observation, in average 35 different horses out of 56 horses (65%) were seen to be resting in a recumbent position. Hence many horses did not assume a recumbent position every night. Seventy-two percent of the recumbency
phases occurred between 0 and 4 am. The capacity of the area for a lying position at one time offered the horses was only exploited to 50%.
The length of the recumbency phase varied significantly between animals and for the individual animals over the duration of the observation period (p<0.001). The average recumbent time per lying phase was 28.8 ± 0.5 (SEM) minutes in the halls (I, II and III), 24.6 ± 0.9 min in the shelter and 20.0 ± 1.9 min on the sand area. The average time spent lying down per horse per day was 91 ± 2.7 min in the halls, 43 ± 2.3 min in the shelter and 27 ± 2.9 min on the sand area (p<0.001). The horses lay down an average of 3.2 times in the halls, 1.7 times in the shelter and 1.3 times in the sand area (p<0.001). Seventy-nine percent of the observed recumbency phases (n= 2410) were seen in the halls. This shows that along with the pastures, the halls played a central role in the recumbency patterns of the horses.
When comparing the halls, a wider variety of horses was observed spending a longer time in recumbency (p<0.0005) more often (p<0.0002) in hall I than in the somewhat smaller halls II and III.
The total time spent per day in recumbency with the head supported was 54.8 ± 1.6 min and hence was ten minutes longer than the total daily time spent in recumbency without the head supported with 45.2 ± 1.8 min. On average the horses spent 27.5 ± 1.1 min in lateral recumbency (p<0.001). Horses were observed to lie in lateral recumbency more often in the halls than on sand area or in the shelter (p<0.001).
The daily total length of time spent in recumbency was found to be significantly longer on bedding (74.3 ± 2.9 min) versus on rubber mats (62.4 ± 2.3 min) (p=0.005). Even though the average number and length of recumbency periods per day and horse, as well as the average time spent in lateral recumbency was greater for the halls, when taking surface area into consideration, it was found that the sheltered area was used the most per surface area for resting in recumbency. Hence it is relevant to state the importance of a shelter as additional lying space in loose housing systems.
The highest number of recumbency phases and the longest time spent daily lying down were seen in the mild months of the year (p=0.013). Temperatures below freezing led to decreased recumbency behavior. The horses observed lay down
almost exclusively in the halls when temperature was below -10°C (p<0.001).
The newcomers (n= 10 horses ≤ 6 months in the stable) to this housing system did not show a diminished recumbency behaviour compared to the other horses (n= 46 horses for 1 to 3 years in the stable). It is apparent that horses that do not have previous experience of rubber mats do not necessitate an adaptation period to use the mats to lay down on, as long as they are introduced into a group of horses that are already comfortable with the use of the mats. Likewise the shavings could help the horses adapt to the new material faster.
The rank of the horse in the herd was determined using a modified “Average Dominance Index”. The horses of low rank showed a significantly lower number of recumbency phases (2.6 compared to 3.4 and 3.1 per horse per day), as well as with 69.3 ± 3.9 min a highly significant shorter by 22 minutes length of recumbency phase when compared to horses of higher rank (each p<0.001). With diminishing rank, the horses lay down less frequently in the halls (2.7 compared to 3.5 and 3.2 recumbency phases per horse per day) and the total daily time spent in recumbency (77.8 ± 5.0 min compared to 97.3 ± 3.9 min und 98.8 ± 5.1 min) diminished significantly (p<0.001). Younger horses were found to lie down more frequently (3.5 compared to 2.6 recumbency phases per horse per day) but also to spend significantly longer periods (103.7 ± 7.6 min compared to 56.1 ± 13.2 min) in recumbency (p<0.001). Younger horses also tended to (90% of recumbency phases of 4 and 5 year old compared to 39% and 70% of 16 until 25 year old) use the halls for recumbent periods of rest (p<0.001). Horse height and weight did not influence recumbency behavior clearly. An interesting correlation was however noted with “body condition score” (BCS). A scale from 1 to 9 was used. The higher the BCS, the more (p=0.0185) and longer (p=0.007) time the animal spent resting in recumbency.
Air ammonia content, air velocity, ambient humidity and temperature measured monthly were within the recommendations of the BMELV (2009). Rubber mats are of no concern to hygiene when used as bedding in loose housing systems with segregated functional areas, as long as sufficient air circulation and proper stable hygiene are present.
The results of the comparative observations of the various bedding materials lead us to conclude that the currently studied rubber mats in combination with a
minimum amount of shaving are accepted by the majority of the horses and therefore are a widely species-appropriate bedding material for horses in loose housing systems.]
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