Abstract: Pferdehaltungssysteme mit angrenzenden Ausläufen gelten als eine sehr tiergerechte
Haltungsform, da sie den Tieren eine gewisse Bewegungsmöglichkeit
bieten. Ziel der vorliegenden Untersuchung war es, zu erfassen, ob der angrenzende
Auslauf selbst einen ausreichenden Anreiz zur Bewegung darstellt und wie sich verschiedene
Bewegungs- und Platzangebote auf die Bewegungsaktivität von Pferden
in einer Gruppen-Auslaufhaltung auswirken. Zudem wurde ermittelt, welche Auswirkung
die Bewegungsform bzw. –intensität auf das Wohlbefinden der Tiere hat.
Der Großteil der in Deutschland gehaltenen Pferde verbringt die meiste Zeit des
Tages im Stall, obwohl mittlerweile bekannt ist, dass Pferde unter natürlichen
Haltungsbedingungen 12 bis 16 Stunden des Tages in Bewegung verbringen. Der
Optimierung der Stallhaltungssysteme gilt daher ein besonderes Interesse.
Zu diesem Zweck wurden von September 2004 bis Oktober 2005 Versuche mit 24
Warmblutstuten im Alter von 1½ bis 3½ Jahren in Einzel- und Gruppen-
Auslaufhaltungssystemen durchgeführt. Jeweils sechs Pferde bildeten eine Versuchsgruppe.
In jeder Gruppe fanden fünf Varianten von einer ca. dreiwöchigen
Dauer statt. Die Gruppenhaltung wurde dabei durch drei unterschiedliche Zusatzbewegungsangebote
(2 Std. Weide / Tag, 2 Std. unbegrünte Koppel / Tag, 1 Std. Freilauf-
Führanlage / Tag) ergänzt. In der Einzel-Auslaufhaltung (Box mit 45 m²-großem
angrenzenden Auslauf) und in einer Versuchsvariante der Gruppenhaltung bekamen
die Pferde hingegen keine zusätzliche Bewegung außerhalb des Stallhaltungssystems
angeboten. Das Gruppenhaltungssystem selbst war durch die räumliche
Trennung der Funktionsbereiche (Liegen, Fressen, Trinken, Bewegen) gekennzeichnet
und der angrenzende Auslauf war 270 m² groß. In einer zusätzlichen Versuchsphase
fand in der Gruppenhaltung eine Erweiterung des permanent zugänglichen
Auslaufs auf insg. 540 m² statt.
Die Bewegungsaktivität wurde mit Pedometern erfasst, die an jeweils einem Hinterbein
der Pferde befestigt wurden und ergänzend fand eine Analyse von Videoaufzeichnungen
statt. Zur Beurteilung der Stressbelastung fanden Messungen der Herz192
Zusammenfassung
frequenzvariabilität (Parameter HF und SD2) und der fäkalen Cortisolmetabolitenkonzentration
statt.
Die Auswertung des Bewegungsverhaltens ergab, dass eine zusätzliche zweistündige
freie Bewegung der Pferdegruppe auf einer Weide zu einer deutlichen
Steigerung der durchschnittlichen Bewegungsaktivität (149,6 Min. / Tag) führt,
ebenso wie eine einstündige Bewegung in einer Führanlage (173,0 Min. / Tag). Eine
unbegrünte Koppel regte die Pferde der Gruppenhaltung hingegen nicht zu vermehrter
Bewegung an (131,6 Min. / Tag), sondern bewirkte z. T. sogar eine Abnahme
der Bewegungsaktivität. In der Gruppen-Auslaufhaltung ohne zusätzliches Bewegungsangebot
war die Bewegungsaktivität ebenfalls gering (125,8 Min / Tag) und
während der Einzel-Auslaufhaltung ohne Zusatzbewegung zeigten die Pferde die
geringste Bewegungsaktivität (102,3 Min. / Tag).
Bei der alleinigen Analyse der Bewegungszeit im Stallhaltungssystem war kein signifikanter
Einfluss der zusätzlichen Bewegung außerhalb des Stallsystems auf die
übrige Fortbewegung feststellbar.
Auch eine Vergrößerung des an den Stall angrenzenden Auslaufs im Gruppenhaltungssystem
hatte keinen steigernden Einfluss auf das Bewegungsverhalten der
Pferde.
Die Stressbelastung der Pferde war in den Varianten der Gruppenhaltung mit zweistündigem
Weidegang (SD2: 82,9 ms; Cortisolmetaboliten: 29,0 nmol / kg Kot) sowie
der einstündigen Bewegung in einer Freilauf-Führanlage (SD2: 99,2 ms; Cortisolmetaboliten:
27,7 nmol / kg Kot) am geringsten. Die Untersuchungen zeigten eine
Stresszunahme in der Gruppenhaltung mit zweistündigem Auslauf auf einer unbegrünten
Koppel ohne Futterangebot (SD2: 101,3 ms; Cortisolmetaboliten:
39,6 nmol / kg Kot) sowie in der Variante der Gruppenhaltung ohne zusätzliches Bewegungsangebot
(SD2: 113,3 ms; Cortisolmetaboliten: 38,4 nmol / kg Kot). Dem
Mittelwert der Gruppe nach zu folgern hatten die Pferde während der Einzelhaltung
ohne Zusatzbewegung eine sehr große Stressbelastung (SD2: 123,8 ms; Cortisolmetaboliten:
37,5 nmol / kg Kot). Ein Vergleich der Gruppen- und Einzelhaltung hinsichtlich
der Herzfrequenzvariabilität hat jedoch gezeigt, dass insg. 70 % der Pferde
während der Haltung in einer Gruppe weniger Stress empfinden. Es gab aber auch
Zusammenfassung 193
Pferde (30 %), die in der Einzelhaltung eine abnehmende Stressbelastung zeigten,
wobei hier der Einfluss der Rangordnung eine entscheidende Rolle zu spielen
scheint.
Durch die Auswertung mehrerer Messparameter (sowohl für Stress- als auch für Bewegungsverhalten)
werden gleichgerichtete Tendenzen bei den Versuchsvarianten
deutlich, allerdings ist eine eindeutige Gewichtung der Parameter nicht möglich.
Somit ist die methodische Vorgehensweise dieser Untersuchung sehr positiv und als
notwendig anzusehen, da die Messdaten auch immer gewissen Schwankungen
durch externe Einflüsse unterliegen.
Allgemein ist festzuhalten, dass Auslaufhaltungssysteme zwar eine gewisse
Anregung zur Bewegung bieten, aber mit maximal vier Stunden (insg. 62 – 248 Min.)
Bewegung pro Tag war der tägliche Anteil an Bewegung sehr viel geringer als
beispielsweise bei Pferden in freier Wildbahn oder ganzjähriger Weidehaltung. Somit
deckt ein Auslaufhaltungssystem trotz getrennter Funktionsbereiche und eines
großen Auslaufs nicht den Bewegungsbedarf der Pferde, wenn keine zusätzlichen
Bewegungsanreize und –möglichkeiten angeboten werden.
Eine zusätzliche Bewegung von Pferden ist nicht nur zur Gesunderhaltung des
Bewegungsapparates und der Körperfunktionen notwendig, sondern auch um das
Wohlbefinden und die Ausgeglichenheit der Pferde zu steigern.
[Horse husbandry systems with close-by discharge are considered to be a very livestock-
friendly housing form, as they offer a certain movement opportunity for the
animals. The aim of the present study was to examine how different movement and
space offerings affect the movement activities of horses in a group horse husbandry
with close-by discharge, and whether the discharge provides itself an adequate
incentive for movement. The impact that the form or rather intensity of movement has
on the wellbeing of the animals was also established.
Most of the horses held in Germany spend most of the day in the stable, although it is
meanwhile known that horses under natural housing conditions are 12 to 16 hours of
the day in motion. Therefore the improvement of stable housing systems applies a
special interest.
For this purpose, 24 warmblood mares, aged from 1½ to 3½ years, were studied in
single and group discharge husbandry systems from September 2004 until October
2005. Six horses formed an experimental group. In every group five variants of approximately
three weeks were proceeded. Thereby the group husbandry was supplemented
with three different additional movement opportunities (2 h pasture / day,
2 h non-grassy pasture land / day, 1 h free range horse walker / day). In the single
discharge husbandry (single box with 45 sq. m-large close-by discharge) and in one
experimental variant of the group husbandry got the horses, however, offered no additional
movement outside the husbandry system. The group husbandry system itself
was marked by the spatial division of the functional areas (lying, eating, drinking,
moving) and the close-by discharge measured 270 sq. m. In an additional phase of
the study, and expansion of the permanently accessible close-by discharge to
540 sq. m was found.
The movement activity was documented with pedometers attached respectively to
one hind leg of the horse and a supplementary analysis of video documentation. To
evaluate the stress exposure measurements of heart frequency variability (parameters
HF and SD2) and of the faecal cortisol metabolite concentration were performed.
Summary 195
The interpretation of the movement behaviour showed that additional two hours of
free movement on a pasture led to a significant increase in the average movement
activity (149.6 min / day), as well as one hour movement in a horsewalker did
(173.0 min / day). The non-grassy pasture land, however, didn’t inspire the horses of
the group husbandry to increased movement (131.6 min / day), but sometimes even
caused a decrease in movement activity. In the group discharge husbandry without
additional movement opportunities the movement activity was also low
(125.8 min / day), and during the single discharge husbandry without additional
movement the horses showed the least movement activity (102.3 min / day).
In analysing only the movement time in the stable system was no significant impact
of the additional movement outside the housing system to the rest of locomotion
ascertainable.
As well an expansion of the close-by stable discharge in the group husbandry system
had no increasing influence on the movement behaviour of the horses.
The stress exposure of the horses was least in the variations of group husbandry
with two hours on a pasture (SD2: 82.9 ms; cortisol metabolites: 29.0 nmol / kg faeces)
as well as one hour of movement in a free range horse walker (SD2: 99.2 ms;
cortisol metabolites: 27.7 nmol / kg faeces). The studies showed a rise in stress in
group husbandry with two hours of movement on a non-grassy pasture land without
feeding opportunity (SD2: 101.3 ms; cortisol metabolites: 39.6 nmol / kg faeces) as
well as in the variation of the group husbandry without additional movement offerings
(SD2: 113.3 ms; cortisol metabolites: 38.4 nmol / kg faeces). Judging from the mean
of the group the horses had a very high stress exposure in the variation of the single
husbandry without additional movement offerings (SD2: 123.8 ms; cortisol metabolites:
37.5 nmol / kg faeces). But a comparison of the group and single husbandry in
terms of the heart frequency variability showed that alltogether 70 % of the horses
experienced less stress if hold in a group. However, some horses (30 %) showed
reducing stress in the single husbandry, whereas here the influence of social hierarchy
seems to play a decisive role.
196 Summary
In consequence of the examination of several measuring parameters (both for stressand
for movement behaviour) parallel aligned tendencies become apparent in the
experimental variants, however, is a unique weighting of the parameters not possible.
Thus, the methodological approach of this study is to be regarde as very positive and
necessary, since the data always vary with some fluctuations by external influences.
In general it can be established that discharge husbandry systems offer some incentive
for the horse to move, but with a maximum of four hours (overall 62 – 248 min) of
movement per day, the daily proportion of movement was much less than, for example,
in the case of wild horses or year-round pasture keeping. Thus, if no additional
movement incentives and possibilities are offered, the discharge husbandry system
doesn’t cover the movement needs of the horse despite separate functional areas
and a large outside discharge.
Additional movement is not only necessary to keep the musculoskeletal system and
bodily functions of the horse healthy, but also to ensure the horse’s well being and
mental balance.]

Abstract: The first weeks of training in young sport horses have been suggested to represent a stressful period and training practises for horses have been questioned recently. So far, only limited data on the stress response of young horses to the initial training are available. Heart rate (HR) provides information on fitness of the horse but is also an indicator of stress or pain. Determination of cortisol metabolites in faeces is a non-invasive technique to determine a prolonged stress response. In our study, three-year-old warmblood sport horse stallions (n=8) were followed through a standardised 10-week classical training programme from lunging to first mounting of a rider and progressing to moderate work. Feed, housing and management were similar for all horses. HR was recorded with a mobile recording System (f810i, Polar, Kempele, Finland) fixed to a girth around the thorax of the horse and was monitored twice weekly from 30 min before to 30 min after training, i.e. including the training period. In addition, cortisol concentrations were determined in faecal samples collected three times daily. Overall basal HR before daily training was 39±2 (SEM) beats/min and mean values did not change significantly over the 10-week study period. Average HR during initial lunging (week 1) was 119±14 beats min and decreased to 95±5 beats/min in week 2. Due to individual variations this decrease did not reach statistical significance. Neither first mounting of a rider (89±10 beats/min) nor an increasing workload (e.g. week 8: 111±4 beats/min) were associated with prolonged increases in mean HR, but transient increases were recorded and the response to mounting of the rider differed markedly between stallions. After daily training, HR decreased rapidly but was slightly, although significantly (p<0.05, Friedman-test) higher than pre-work values (46±2 beats/min). Cortisol metabolite concentrations in faeces tended to decrease during the period of lunging, were not increased when the horses were first mounted by a rider but rose slightly with an increasing work load during the last 4 weeks of the 10-week training period. In conclusion, based on HR and faecal cortisol metabolite concentrations, the initial training of sport horse stallions in the classical German training system is not associated with major stress for the horse. The increase in HR during training is due to physical exercise itself and not associated with specific situations of the training programme.
Supported by a fellowship from Stiftung Forschung für das Pferd to AS

Abstract: The colours of the horses have long been a subject of interest to owners and breeders of horses as well as to scientists. Though, the colour of horses has little to do with its performance, it is a primary means of identification and also the first indicator of questionable parentage. Probably the ancestral colour of the horse was a black-based pattern that provided camouflage protection against predators. Horse colours are mostly controlled by genes at 12 different loci. The three basic colours of horses are black, bay and chestnut. The genetic control of the basic colours of horses resides at two genetic loci, namely Extension (E) and Agouti (A) loci. Among the basic colours bay is dominant to black and both are epistatic to chestnut. Dilution of basic colours of horses as a result of four colour dilution genes such as cream dilution, dun, silver dapple and champagne resulted in extensive array of possible colours of horses. The most widespread and familiar of the horse colour dilution gene is the one that produces the golden body colour and are called as palomino or buckskin based on the colour of the points. The grey coat colour is due to the presence of dominant gene (G) at the grey locus. Grey is epistatic to all coat colour genes except white and a grey horse must have at least one grey parent. Roan is due to a dominant gene (Rn) at roan locus and this combines with any base colour to produce the various shades of roan pattern. White coat is due to a single dominant gene (W) and it is epistatic to the genes controlling all other colours. White marking in the face and legs are due to genetic and non-genetic factors. Several genes are involved in producing white markings. During recent years, comparative genomics and whole genome scanning have been used to develop DNA tests for different variety of horse colours. Molecular genetic studies on coat colour in horses helped in identification of the genes and mutation responsible for coat colour variants. In future, this will be applied to breeding programmes to reduce the incidence of diseases and to increase the efficiency of race horse population.

Abstract: Social network analysis is used widely in the social sciences to study interactions among people, groups, and organizations, yet until now there has been no book that shows behavioral biologists how to apply it to their work on animal populations. Exploring Animal Social Networks provides a practical guide for researchers, undergraduates, and graduate students in ecology, evolutionary biology, animal behavior, and zoology.
Existing methods for studying animal social structure focus either on one animal and its interactions or on the average properties of a whole population. This book enables researchers to probe animal social structure at all levels, from the individual to the population. No prior knowledge of network theory is assumed. The authors give a step-by-step introduction to the different procedures and offer ideas for designing studies, collecting data, and interpreting results. They examine some of today's most sophisticated statistical tools for social network analysis and show how they can be used to study social interactions in animals, including cetaceans, ungulates, primates, insects, and fish. Drawing from an array of techniques, the authors explore how network structures influence individual behavior and how this in turn influences, and is influenced by, behavior at the population level. Throughout, the authors use two software packages--UCINET and NETDRAW--to illustrate how these powerful analytical tools can be applied to different animal social organizations.
Darren P. Croft is lecturer in animal behavior at the University of Wales, Bangor. Richard James is senior lecturer in physics at the University of Bath. Jens Krause is professor of behavioral ecology at the University of Leeds.
Reviews:
“Exploring Animal Social Networks shows behavioral biologists how to apply social network theory to animal populations. In doing so, Croft, James, and Krause illustrate the connections between an animal's individual behaviors and how these, in turn, influence and are influenced by behavior at the population level. . . . Valuable for readers interested in using quantitative analyses to study animal social behaviors.”--Choice
“[T]his volume provides an engaging, accessible, and timely introduction to the use of network theory methods for examining the social behavior of animals.”--Noa Pinter-Wollman, Quarterly Review of Biology
“The book is a useful 'handbook' providing detailed, stepwise procedures sufficient to allow the reader to address a broad range of questions about social interactions. . . . The book includes numerous examples of the kind of research questions one might ask, and, thus, it allows the reader to find the analysis that best fits the data set to be analyzed. Thus, even readers with minimal prior knowledge of social network analysis will be able to apply this approach. And if further assistance is needed, the authors provide numerous references to specific procedures that have been used by others.”--Thomas R. Zentall, PsycCRITIQUES
Endorsements:
“An important and timely addition to the literature. This book should be readily accessible to researchers who are interested in animal social organization but who have little or no experience in conducting network analysis. The book is well-written in an engaging style and contains a good number of examples drawn from a range of taxonomic groups.”--Paul R. Moorcroft, Harvard University
More Endorsements
Table of Contents:
Preface vii
Chapter 1: Introduction to Social Networks 1
Chapter 2: Data Collection 19
Chapter 3: Visual Exploration 42
Chapter 4: Node-Based Measures 64
Chapter 5: Statistical Tests of Node-Based Measures 88
Chapter 6: Searching for Substructures 117
Chapter 7: Comparing Networks 141
Chapter 8: Conclusions 163
Glossary of Frequently Used Terms 173
References 175
Index 187
Subject Area:
* Biological Sciences

Abstract: Horses have been considered to rely on human gesticular cues (McKinley and Sambrook 2000, Anim Cogn 3:13-22; and recently Maros et al. 2008, Anim Cogn 11:457-466), however large variability among individuals tested in two-ways object choice tasks was found. Part of the horses in those studies (40 and 26 %, respectively) even failed to pass adequately through the training session which preceded the testing phase and served to learn a horse to carry out a task. Therefore, we alternated the experimental design designed by McKinley and Sambrook (reduced number of testing trials to 10 per horse to keep its attention, applied just one, a dynamic-sustained pointing cue with touching the bucket, etc.), and tested an effect of training method, sex, age, and learning on proportion of correct choices. We hypothesised, that horses trained by “traditional” method (TTM) will get lower score than those experienced with “horsemanship-based” methods (HTM), being characterized by closer and more frequent human-horse contact and also extended exercising “from the ground” with frequent using of arms cues. Despite simplification of the methods, only about 60 % of tested horses passed through the training phase (i.e., learned to come to and upturn the bucket with hidden treat). Successful completion of training phase was reached regardless of age or sex of a horse, but by the training method; HTM horses ran better compared to TTM ones. No significant effect of age, sex, or learning (i.e., trial order within all 10), and training method as well was found on proportion of correct trials in the testing phase. Horses made a correct choice in more than 70% of trials. Individual scores ranged from 50 to 100 %. In conclusion, horses showed high level of comprehension of human pointing gesture, regardless of their sex or age. No effects of training method or learning process within a test suggest low impact of handling and learning on the level of comprehension at least of the most vivid human pointing gesture. Horses trained by methods based on “natural human-horse communication” did enhance cooperation with people.