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Sueur, C., Deneubourg, J. - L., & Petit, O. (2012). From Social Network (Centralized vs. Decentralized) to Collective Decision-Making (Unshared vs. Shared Consensus). PLoS ONE, 7(2), e32566 EP -.
Abstract: <p>Relationships we have with our friends, family, or colleagues influence our personal decisions, as well as decisions we make together with others. As in human beings, despotism and egalitarian societies seem to also exist in animals. While studies have shown that social networks constrain many phenomena from amoebae to primates, we still do not know how consensus emerges from the properties of social networks in many biological systems. We created artificial social networks that represent the continuum from centralized to decentralized organization and used an agent-based model to make predictions about the patterns of consensus and collective movements we observed according to the social network. These theoretical results showed that different social networks and especially contrasted ones – star network vs. equal network – led to totally different patterns. Our model showed that, by moving from a centralized network to a decentralized one, the central individual seemed to lose its leadership in the collective movement's decisions. We, therefore, showed a link between the type of social network and the resulting consensus. By comparing our theoretical data with data on five groups of primates, we confirmed that this relationship between social network and consensus also appears to exist in animal societies.</p>
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Klingel, H.. (2012). Social Organisation and Social Behaviour of the Equids. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: In contrast to the great similarity in behaviour and ecology of the 6 extant Equid species, 2 distinct types of social organisation have evolved, and both are adapted to life in semi-arid to arid regions where environmental conditions force them to migrate seasonally or opportunistically.
The ranges of the various species overlap: Mountain Zebra Equus zebra and Plains Zebra E. quagga in South Africa and Namibia, Plains Zebra and Grevy's Zebra E. grevyi in Kenya and Ethiopia, Grevy's Zebra and African Wild Ass E. africanus in Ethiopia, Asiatic Wild Ass E. hemionus and Przewalski Horse E. przewalski in Mongolia and China. Although, in the overlap zones, individuals of the different species are using the same resources like water and grazing next to each other, they rarely make closer contacts.
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In the type 1 species, Horse, Plains Zebra and Mountain Zebra, the adults live in non-territorial, stable, one-male families and as single bachelors and in bachelor groups. Family stallions have the exclusive mating rights with the mares in their harems. These consist of up to 6 unrelated mares plus their offspring, totalling up to 20 members.
Mares stay in their harem until death. Stallions' tenure is from age 5-6 years, i.e. when they succeed in controlling a harem, for close to life time, but are replaced when dead or incapacitated. Harems are stable even in the absence of a stallion, indicating voluntary membership. Adolescent mares leave their parental families to become members of another harem.
In Plains Zebra the adolescent mares are abducted, during an oestrus, by suitors who fight the defending family stallion/father. Successful stallions are bachelors who start a family, or family stallions enlarging their harem. Young stallions leave their parental families voluntarily at age 2-3 years and join bachelor stallion groups from where the family stallions are recruited.
An individualised dominance hierarchy excists with the stallion in the alpha position. It is based on individual knowledge and recognition of the members.
In the type 2 species Grevy's Zebra, African Wild Ass and Asiatic Wild Ass adult stallions monopolise territories in which they have the exclusive mating rights. Stallions are tolerant of any conspecifics entering their territory. Bachelor stallions behave subordinately – or fight for the possession of the territory which is a prerequisite for reproduction.
Mares join up to form anonymous and unstable groups or herds. The only stable unit is of a mare and her offspring. In Grevy's Zebra mares with foal join preferentially conspecifics of the same soial status, as do mares without foal.
Matings take place inside the territory. There is no lasting relationship of the mare with a particular stallion, and the mare may be mated by any stallion whose territory she is visiting.
Territories measure up to 10 or more square kilometres, and tenure is for several years.
Grevy Zebra territorial owners leave their territories for a few hours to visit a water hole, or for months when grazing and water conditions are below requirements, and re-occupy it upon return, unchallenged.
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Klingel, H.. (2012). Soziale Organisation und Sozialverhalten der Equiden. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Verhalten und Ökologie der 6 rezenten Equiden sind in vieler Hinsicht identisch, jedoch in der Sozialen Organisation haben 2 deutliche verschiedene Formen evoluiert, die beide an das Leben in den semi-ariden und ariden Lebensräumen angepasst sind, wo sie zu säsonalen oder opportunistischen Wanderungen gezwungen sind.
Die Verbreitungsgebiete der verschiedenen Arten überlappen, in Südafrika und Namibia von Bergzebra Equus zebra und Steppenzebra E. quagga, in Kenya und Äthiopien von Steppenzebra und Grevy-Zebra E. grevyi, in Äthipien und Somalia von Grevy-Zebra und Afrikanischem Wildesel E. africanus, in China und der Mongolei Asiatischer Wildesel E. hemionus und Przewalski-Pferd E. przewalskii. Obwohl die Vertreter der verschiedenen Arten in den Überschneidungsgebieten die gleichen Ressourcen wie Wasser und Weide nutzen, nehmen sie kaum Kontakt zueinander auf.
Die Vertreter von Typ 1, Steppenzebra Equus quagga, Bergzebra E..zebra, Pferd E przewalskii, leben in nicht-territorialen , dauerhaften 1- Hengst- Familien, in Hengstgruppen und als Einzelgänger.. Die Familienhengste haben die alleinigen Paarungsrechte mit den Stuten in ihrem Harem. Dieser besteht aus bis zu ca. 6 nicht-verwandten Stuten nebst ihren Nachkommen und kann bis 20 Mitglieder haben.
Stuten bleiben bis zu ihrem Tod im Harem..Hengste können mit 5-6 Jahren einen Harem erobern oder gründen, können gleichfalls bis zum Tod die Familie begleiten, werden aber meist vorher von einem anderen Hengst ersetzt. Harems sind auch ohne Hengst stabil, ein Hinweis, dass die Stuten freiwilling im Harem sind und bleiben.. Junge Stuten verlassen ihre elterliche Familie und schliessen sich einem anderen Harem an..Beim Steppenzebra werden die Jungstuten während eines Östrus (Rosse) von Bewerbern entführt, gegen den Widerstand des Familenhengstes = Vaters. Bewerber sind Junggesellen, die so eine Familie gründen, und Familienhengste, die so ihren Harem vergrössern. Junghengste verlassen mit 2-3Jahren ihre elterliche Familie und schliessen sich Jungesellengruppen an, aus denen sich die Familenhengste rekrutieren.
In der Gruppe besteht eine Rangordnung mit dem Henst in der alpha-Position. Sie beruht aud individuellem Kennen und Erkennen der Mitglieder.
Bei Typ 2, Grevy-Zebra, Afrikanischer und Asiatischer Wildesel, monopolisieren Hengste über Jahre Territorien von 10 und mehr km2 , in denen sie die alleinigen Paarungsrechte haben. Territoriale Hengste tolerieren Artgenossen, auch erwachsene Hengste, soweit diese sich unterlegen verhalten. Oder sie stellen sich zum Kampf um den Besitz des Territoriums, eine Vorbedingung für die Fortpflanzung. Stuten im Östrus können von mehreren Hengsten begattet werden, wenn sie sich in deren Territorien aufhalten bzw diese durchwandern.
Stuten und Fohlen und nicht-territoriale Hengste schliessen sich zu anonymen instabilen Gruppen oder Herden zusammen. Feste dauerhafte Bindungen bestehen nur zwischen Stute und Fohlen. Hengste verlassen ihr Territorium für Stunden, Tage, im Extrem auch Monate, um zu Wasserstellen oder Weidegründen zu ziehen, sind aber bei Rückkehr wieder unangefochtene Besitzer.
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Chittka, L., & Dyer, A. (2012). Cognition: Your face looks familiar. Nature, 481(7380), 154–155.
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Ahmadinejad, M., Tavakoli, S. (2012). Common injuries in athletic horses in Tehran‘s riding clubs. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press).
Abstract: Various forms of intensive sport activities places stresses on the musculoskeletal system of the horse while involve in any forms of the activity (race &/or training). The musculoskeletal system of the horse has an inherent ability to adapt to the demands of high speed exercise, though if a threshold in adaptive capacity is exceeded, then some forms of damages to the structures of the musculoskeletal system may result. In case, if the insult (race &/or training) continued, it may worsen the repair and adaptation process and put the horse at risk of more serious musculoskeletal injury.
The result of this research describe the finding of the study performed in different breeds of horses involved in various types of activity in Tehran’s riding clubs, concentrating on the types of injuries observed in those horses. The study was then focused on the types of injuries observed in various activities (events) horses involved in.
Totally 400 horses took part in various activities during race season (March – September) in Tehran’s riding clubs, out of which 26 horses injured, in most of which musculoskeletal system of the fore limbs were involved.
From the sexual aspect of the study the percentages of the stallions were more (54%) when compared to the mares (46%). In this study the relation between the sex, breed, age and the weight of the horses with anatomical site of the injury, outcome of the injury, climate and the type of the event (jumping, polo etc.) were studied and compare with each other.
Bibliography:
Hill AE, Stover SM, Gardner IA, Kane AJ, Whitcomb MB, Emerson AG, 2001. Risk factors for and outcomes non catastrophic suspensory apparatus injury in Thoroughbred race horse. J.A.V.M.A. 218, 1136-44
Johnson BJ 1993. A look at race horse breakdowns. J.Eq.Vet.Scie. 13, 129-32
Morse SJ. 1999. A longitudinal study of racing thoroughbreds; performance during the first year of racing. Aust.Vet.J. 77, 105-12
Peloso JG, Mundy GD, Cohen ND. 1994. Prevalence of, and factors associated with, musculoskeletal racing injuries of thoroughbreds. J.A.V.M.A. 204, 620-6
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Bouskila, A., Renan, S., Speyer, E., Ben-Natan, D., Zaibel, I., & Bar-David, S. (2012). Group composition and behavior of reintroduced Equus hemionus near a water source in the Negev Desert. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: The Asiatic Wild Ass, Equus hemionus, was once abundant in western Asia. The species declined due to hunting and habitat loss. Between 1982-93 38 E. hemionus (21? 17?) that originated from Iran and Turkmenistan were reintroduced to the Negev Desert, Israel. Saltz, Rubinstein and co-workers studied the released population till 1999. The current population in the Negev is estimated at more than 200 individuals, yet, their social and genetic structures are not known. Here we report group composition and behavior of E. hemionus near a water sources from the 2010 and 2011 field seasons, which is part of a wider study of the mating system and genetic diversity. We recorded and videotaped group composition and social interactions from a shelter, 150m from the water source. We recorded a total of 377 observations, in which 251 only males were observed, in 105 observations we observed females and juveniles, and only in 21 cases we observed a mixed group of females with at least one male. Not all wild asses were individually identified, but so far, we analyzed data from 69 individual profiles (based on photos), and recorded in which groups were they videotaped. Before reaching the water source, wild asses often aggregate in large groups and wait for the first few individuals to approach cautiously the water, and only then the rest of the individuals make a swift final approach. We did not consider these aggregations as social groups. We defined a group when individuals approached or left together the valley in which the water source is located. In a few encounters between E. hemionus and wolves (around sunset) we noticed that the wild asses showed interest in the wolves and increased alertness, but the wolves did not approach the equids under these conditions. Female groups (including those with a male) were larger than male-only groups (range 2-49 and 1-34, respectively; P =0.0191). From records of individuals observed more than once, individuals appear on different days in groups of various sizes and compositions, suggesting a social structure with a certain degree of fission-fusion. The mean proportion of juveniles per female was 0.57 and this value is higher than the average found in the 1990’s study (0.5). Apart from the proliferation of the population, an important difference between the earlier and the current study stems from the fact that the E. hemionus in the Negev Desert expanded their range and it includes now the Negev Highlands, an area with slightly more mesic and stable conditions. Except for Sep., fewer adult females were observed compared to males (P=0.028). Different daily activity patterns of the two sexes may explain this observation. These results will be combined with the genetic work and will contribute to the assessment of population viability.
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Novotný, F., Noskovič, ová, J., Valocký, I., Pošivák, J., Boldižár, M., et al. (2012). Differences of biochemical and haematological indices in the aging process in cold-blooded horses Norik Muráň type. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: The aim of was to compare of biochemical and haematological parameters in the aging process in a cold-blooded mares breed Norik Muráň type. 27 of breeding mares Norik Muráň type without pathological symptoms in horse breeding farm in Dobšiná (Slovakia) were used in this study. Mares were divided by age into four groups: A (n = 7, 5-8 years), B (n = 6, 9-15), C (n = 7, 16-20) and D (n = 7, 21-23). Blood samples were collected from v. jugularis externa by needles (Vacutainer ® Precision Glide ™, BD Diagnostics, USA) in serum tubes (Serum-SST TM II Advance, BD Diagnostics, USA) in the morning hours, kept at 8 to 10 °C and analyzed as soon as possible. Biochemical parameters of blood serum like aspartate aminotransferase (AST), alkaline phosphatase (ALP), creatinine (CREA), urea (Urea), albumin (ALB) and glucose (Glu) were analyzed using biochemical analyzer Cobas c 111 (Roche, Switzerland). Reference values were determined by Laboratory of Clinical Biochemistry and Haematology (UVMF, Košice). Were used a same nutrition for all mares. The results were statistically processed using Student\'s t-test. The concentrations of AST decreased in mares with aging (A=5.69 ± 1.13 μkat/l; B=5.36 ± 0.9 μkat/l; C=5.13 ± 1.1 μkat/l), but in the oldest mares (D=5.88 ± 1.37 μkat/l). were higher than the youngest age group A. Were found no significant differences between groups (P> 0,05). The concentrations of ALP increased with age (A=2.47 ± 0.3 μkat/l; C=2.66 ± 0.43 μkat/l; D=2.77 ± 1.17 μkat/l), but in the middle age mares were found (B= 2;44 ± 0.46 μkat/l) (P> 0,05). Crea concentrations had a decreasing trend (A=139.1 ± 37.49 μmol/l; B=118.45 ± 23.18 μmol/l; C=119.31 ± 19.85 μmol/l; D=111.59 ± 21.08 μmol/l) (P> 0,05). Urea increased with age (A=7.88 ± 2.04 mmol/l, B= 7.97 ± 0.8 mmol/l, D= 8.29 ± 1.23 mmol/l) except C (7.76 ± 0.85 mmol/l) (P> 0,05). ALB decreased with age (A=31.34 ± 3.24 g/l; B=30.03 ± 2.41 g/l; C=30±2.77 g/l; D=29.67± 2.85 g/l) (P> 0,05). Also glucose concentrations were lower in older mares (A=4.51 ± 0.99 mmol/l; B=4.69 ± 1.05 mmol/l; C= 4.69 ± 1.05 mmol/l; D =4.03 ± 0.64 mmol/l) (P> 0,05). Significantly differences were found in leukocytes between group A =2,76±1,82 g/l versus groups B=6,74±0,56 g/l, C =6,46±1,14 g/l and D =6,13±1,61 g/l (P<0.05), also in neutrophiles between A=2,06±1,26 109/l versus B= 3,47±1,17 109/l, C =3,12±0,9 109/l and D =2,88±0,71 109/l (P<0.05). Were found significantly differences in eosinophiles between group A =0,06±0,09 109/l versus groups B=0,21±0,17 109/l, C=0,19±0,1 109/l and D=0,12±0,11 109/l (P<0.05), also in lymphocytes between A=4,59±1,59109/l versus B =2,95±1,04109/l, C=2,99±1,14109/l and D=2,65±1,87109/l (P<0.05). This research evaluated selected biochemical and haematological parameters of breed mares Norik Muráň type of different ages. We found that age affects these indices in mares Norik Muráň type. Data from this study may enhance our understanding of the biochemical parameters in this species, allowing a veterinarian to fix the interpretation of laboratory data and give these animals the appropriate care. This study was supported by grant from the Ministry of Education VEGA 1/0498/12 of the Slovak Republic.
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Mshelia, W. P., Abdussamad, A. M., Onoja, I. I., Victoria, S.Q., & Richard, E. E. (2012). Husbandry and Management Practices in Domestic horses in Northern Nigeria and their Clinical Implications. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: This study was conducted to identify common husbandry and management practices associated with domestic horses in Northern Nigeria. Fifty (50) of the horse was purposely selected as units of analysis. Primary data was generated by means of a pre-tested, semi-structured questionnaire administered to the sampled respondents. A simple inductive statistics was applied to the primary data. The study revealed that the whole facilities studied 50(100%) had a prior experience with horses. A large number of horses, mostly West African Dongola and West African Barb are kept solely for pleasure or ceremonial purposes (60%). While the other breeds of horses like Argentine (6%) and South Africa polo ponies (2%) are kept for polo. Recently, the Sudan country-bred (4%) and Western Sudan pony (6%) have found a place in West African polo. Other breeds found within the facilities studied are Argentine criollo; Nigerian ponies and various crosses. Only 10% of the facilities had breeding stocks with only 2% carrying out artificial insemination while 8% do natural mating. The housing management system includes stables (40%) and open fields (60%) where horses are tethered. Bedding materials includes straws (50%); sand (20%) and wood shavings (30%). Feed grade provided include a combination of rations-bran; cracked grain and hay (40%), Bran; cracked grain and legumes (48%) and Bran and hay (12%), all feed combination administered along with fresh grass. Watering and feeding practices involves provision of feed and water twice daily (50%) and while others provide it adlib (25%). Feeding horses with various additives accounted for 19% of the studied facilities. The health status as shown by the body condition score ranges from II-IV/V (88%) of the population studied. Routine dental care is regular (30%) with all the facilities while others (70%) are not irregular. Grooming is common in all the facilities especially within the performance horse circle. Routine hoof care including trimming and shoeing is common in 26% of the facilities while hoof trimming without shoeing is a common practice in 74% of the facilities. Orthodox medicine practiced in 80% of the studied area. While ethnoveterinary consist of 10%, while a combination of orthodox and ethnoveterinary medicine was common in 10% of the study area. Vaccination against African horse sickness equine influenza and tetanus is common in the various equine communities.Though 16% of the population do not vaccinate against any known disease. Parasite control program include pasture hygiene (4%); interval dosing (10%); continuous in-feed (4%); selective dosing (40%) and strategic dosing constitute 42%. Exercise is a common practice but intensity and duration is not strictly adhered to especially during tendon injuries. Manure management differs from facility to facility- some dispose manure within the facilities (40%) while others dispose it outside the facilities (60%). A number of clinical signs like limping, coughing, ocular and nasal discharge, swellings on the body, abnormal mucous membrane, fever, ventral oedema and reluctance to move, foul respiratory odour was observed. Clinical cases like laminitis; pigeon fever; bran disease; colic; African horse sickness; exertional rhabdomyolysis; sinusitis; piroplasmosis; dermatomycosis and tumours was observed. KW -
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Hinrichs, T. (2012). Group management in Active-Stables. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: In active stabling the horses live in a group and are in constant social contact with their equine companions. Separate, dedicated areas define the concept. The key element of active stabling is the automatic feeding of hard feed, minerals and forage. This ensures the correct level of feeding and encourages the horses to increase their level of activity. The organisation of the dedicated areas in active stabling is dependent on a number of factors, such as the given facilities, the planned group sizes and the commercial and working aspects.
The ongoing acquisition of knowledge from science and research, practical experience from the horse industry, and the relevant national guidelines and conditions for keeping horses, form the basis for the planning of active stabling.
For example, in Germany, an important contribution to the further development of the active stabling concept is coming from the current research by Dr Zeitler-Feicht and her team into automatic feeding systems and the arrangement of areas to lie down in the quiet space. Together they run around 500 active stabling facilities, and they made a significant contribution to the 2009 guidelines for horse husbandry in the animal protection regulations.
At the ISEM 2012, practical examples of group management in active stabling will be presented. The aim of the participants is to achieve a continuing improvement in horse husbandry, combining the requirements of animal protection with the uses of the horses.
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Kultus, K. B., & Balzer, H. - U. (2012). Analysis of Human-Horse-Relation. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: The relation between humans and animals is one of the most famous factors for animal welfare in modern housekeeping systems. Words like intuition and empathy in exposure to the horse are difficult to describe, to measure or to teach. In German speaking countries there is the sentence: a good rider knows what the horse will do before it can do it; a bad rider only reacts to what the horse has done. By using the monitoring systemsmardwatch® in connection with chronobiological regulation diagnostics it becomes possible to get insight in the interaction between human and horse.Thesmardwatch® enables measuring of so called psycho-physiologicalparameters likeskin resistance, skin potential, electromyogram and skin temperature, measured 10 times per second; it also registersbehaviorinformation as 3D-acceleration and -position and over this environment information like temperature, noise and brightness. Cutting hooves, cleaning and riding a horse are monitored for example. The data were analyzed under distinct aspectsby chronobiological regulation diagnostics developed byBalzerand Hecht (2000). The physical and vegetative activities of the human and the animalwhere pointed out separately and in their interactionat different levels. Very interesting is the influence of different humans on one horse or the influence of one human on distinct horses. The synchronies or asynchronies in the behavior of different human-horse-pairs could be proved at the level of their vegetative functions. While riding phases of exhaustion of the horse could be shown just as the increasingactivity of the rider to compensate this exhaustion. The method could be a basic approach to develop new training methods which agree with individual rhythms of riders and horses to optimize their achievement.These analysis are not only important for riding, they also give useful directions for daily contact with horses. So it will be possible to detect harmony/disharmony between human and horse for their pairing in order to teach them and to buy or sell a horse, respectively. KW horse, human, chronobiology, synchronisation, smardwatch
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