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Dugatkin, L.A.; Godin, J.-G.J. |
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Title |
Female mate copying in the guppy (Poecilia reticulata): age-dependent effects |
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Journal Article |
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1993 |
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Behavioral Ecology |
Abbreviated Journal |
Behav. Ecol. |
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4 |
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4 |
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289-292 |
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mate choice, copying, guppy, Poecilia reticulata |
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Virtually all studies of mate choice to date have assumed that females choose mates independent of one another. Social cues, however, such as the mate choice of conspecifics, may also play an important role in such decisions. Previous work has shown that female guppies of similar age copy each other's choice of mates. Here we examine the effect of relative age on mate choice copying in the guppy, Poecilia reticulata, and examine whether younger individuals are more likely to copy the mate choice of older conspecifics than vice versa. Results indicate that younger females copy the mate choice of older females, but older individuals do not appear to be influenced by the mate choice of younger individuals. |
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Equine Behaviour @ team @ |
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2181 |
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SYLVAIN GAGNON,FRANCOISY. DORE |
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Title |
Search behavior of dogs (Canis familiaris) in invisible displacement problems |
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1993 |
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Animal Learning & Behavior |
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Anim Learn. & Behav. |
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21 |
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3 |
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246-254 |
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Gagnon and Dor (1992) showed that domestic dogs are able to solve a Piagetian object permanence
task called the invisible displacement problem. A toy is hidden in a container which is
moved behind a screen where the toy is removed and left. Dogs make more errors in these problems
than they do in visible displacement tests, in which the object is hidden directly behind
the target screen. In Experiment 1, we examinedcomponents ofthe standard procedure of invisible
displacements that may make encoding or retention of the hiding location more difficult than
it is in visible displacements. In Experiment 2, we compared dogs performances in visible and
invisible displacement problems when delays of 0, 10, and 20 sec were introduced between the
objects final disappearance and the subjects release. The results revealed that dogs poorer performance
in invisible displacement tests is related to the complex sequence of events that have
to be encoded or remembered as well as to a difficulty in representing the position change that
is signaled, but not directly perceived. |
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refbase @ user @ |
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538 |
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Author |
Veissier, I. |
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Title |
Observational learning in cattle |
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Journal Article |
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Year |
1993 |
Publication |
Applied Animal Behaviour Science |
Abbreviated Journal |
Appl. Anim. Behav. Sci. |
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35 |
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3 |
Pages |
235-243 |
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Four experiments were designed to find evidence of observational learning in cattle. The experiments were run on ten experimental heifers, each observing a demonstrator mate performing a task, and on ten control heifers, each observing a non-demonstrator mate. The mates and observers were separated by wire netting in Experiments 1-3, but were in the same room in Experiment 4. The task to be learned was to push a panel to get food into a box. All naive animals were able to observe while their mate performed the task. The observers in Experiments 1 and 4 were Salers heifers that had no prior experience of the testing room; those in Experiment 2 were Salers heifers that were accustomed to the room; those in Experiment 3 were Aubrac or Limousin heifers that had already eaten in the room.
The behaviour of the observers was influenced by their mates: activity at or near the boxes was enhanced by the presence of demonstrators in Experiment 2 (box contacts: 38.0 +/- 16.2 vs. 22.1 +/- 11.9 for experimental and control heifers, respectively; P<0.05), while activity in other parts of the room in Experiment 3 was enhanced when non-demonstrator mates were present (wall sniffing: 5.4 +/- 13.9 vs. 13.9 +/- 13.7; P<0.05). Overall, 26 experimental heifers vs. 19 controls learned the task (P>0.05). The time spent eating was longer when the observer only had visual contact with a demonstrator (Experiment 1: 15.9 +/- 1.6 vs. 11.6 +/- 1.8 min), but was lower when physical contacts with the demonstrator were possible (Experiment 4: 4.6 +/- 8.8 vs. 5.4 +/- 2.2 min; P<0.05).
Ten out of the 11 Limousin heifers learned the task, compared with only three out of the nine Aubrac heifers (P<0.05). The latter spent more time near the door and sniffed the walls more often than the former (2.0 +/- 1.9 vs. 0.4 +/- 0.6 min, P<0.05, and 18.1 +/- 13.4 vs. 2.7 +/- 6.5 min, P<0.01), as though they were trying to flee the situation.
When animals observed a demonstrator, their attention was drawn to stimuli involved in the task but acquisition of knowledge was not greatly improved. |
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Equine Behaviour Team @ birgit.flauger @ |
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4325 |
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Author |
RÖHRS, M.; EBINGER, P. |
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Title |
Progressive und regressive Hirngrößenveränderungen bei Equiden |
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1993 |
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Z zool Syst Evolut forsch |
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31 |
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233-239 |
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from Professor Hans Klingels Equine Reference List |
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yes |
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1513 |
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Genov, P.W.; Kostava, V. |
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Title |
Untersuchungen zur zahlenmäßigen Stärke des Wolfes und seiner Einwirkung auf die Haustierbestände in Bulgarien |
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Journal Article |
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Year |
1993 |
Publication |
Zeitschrift für Jagdwissenschaft |
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39 |
Issue |
4 |
Pages |
217-223 |
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Die Untersuchung wurde in der Zeitspanne von 1984 bis 1988 durchgeführt. Es wurden die Protokolle des Staatlichen Versicherungsinstituts benutzt, die Angaben für Raubüberfälle von Wölfen auf Haustiere beinhalten (Tabelle 1). Außerdem wurden Angaben über die während dieser Zeitspanne erlegten Wölfe zusammengefaßt. Die Abschußzahlen lauten: 1984 – 163, 1985 – 147, 1986 – 179, 1987 – 211 und 1988 – 220 Tiere. Die Anzahl der in den einzelnen Gebirgen lebenden Wölfe wurde nach einer Umfrage festgestellt. Für die in Betracht kommenden Gebirge werden folgende Bestandszahlen angenommen: Rhodopen -- 60-80 Individuen, 189 bis 264 km2 pro Tier, Rila- und Piringebirge -- 60-80 Tiere, 109 bis 145 km2 pro Tier, Ossogowo-Belassiza Gebirgssystem -- 40-50 Individuen, 57-70 km2 pro Tier, West- und Mittelbalkan -- 35-38 Wölfe, 200 km2 pro Tier. Dazu kommen noch 10-15 Wölfe im Flußbecken von Beli Lom und etwa 20 Exemplare in Strandscha- und Sakargebirge. Insgesamt lebten in Bulgarien im Jahre 1988 etwa 260-330 Wölfe (Abb. 1). |
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1439-0574 |
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Equine Behaviour @ team @ Genov1993 |
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6686 |
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Author |
Mitchell R |
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Title |
Mental models of mirror self-recognition: two theories |
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1993 |
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New Ideas Psychol. |
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11 |
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211 |
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Equine Behaviour @ team @ |
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3019 |
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Petherick, J.C.; Seawright, E.; Waddington, D. |
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Influence of motivational state on choice of food or a dustbathing/foraging substrate by domestic hens |
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1993 |
Publication |
Behavioural Processes |
Abbreviated Journal |
Behav. Process. |
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28 |
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3 |
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209-220 |
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Food; Learning; Litter; Motivation; Poultry; Preference |
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Domestic hens were trained to run a Y-maze and make an association between differently coloured doorways and access to food pellets or sand. The hens were tested for their choice of doorway when the goals were not visible from the choice point and when they were food or sand deprived. Hens made the choice appropriate to their deprivation state (correct choice) significantly more often for food than sand and were faster at choosing and entering the goal box when food deprived. In a follow up experiment, the goals were visible from the choice point. Again the hens chose correctly significantly more often when food than sand deprived and made the choice and entered the goal box faster when food deprived. Thus, failure to choose sand in the first experiment was not due to an inability to learn the association, but appears to result from a strong motivation to feed in the Y-maze, even when not food deprived, and a weak motivation to dustbathe or forage, even when sand deprived. |
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Equine Behaviour @ team @ |
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3608 |
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Ratzlaff, M.H.; Wilson, P.D.; Hyde, M.L.; Balch, O.K.; Grant, B.D. |
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Relationship between locomotor forces, hoof position and joint motion during the support phase of the stride of galloping horses |
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1993 |
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Acta Anatomica |
Abbreviated Journal |
Acta Anat (Basel) |
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146 |
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2-3 |
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200-204 |
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Animals; Equipment Design; Hoof and Claw/*physiology; Horses/*physiology; Joints/*physiology; *Locomotion; Motor Activity/*physiology; Physiology/instrumentation; *Posture; Shoes; Transducers |
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Three methods were used simultaneously to determine the relationships between the vertical forces exerted on the hooves and the positions of the limbs and hooves at the times of peak vertical forces from 2 horses galloping on a track straightaway. Vertical forces were recorded from an instrumented shoe, fetlock joint motion was measured with an electrogoniometer and the angles of the carpus, fetlock and hoof were determined from slow-motion films. At hoof contact, the mean angles of the carpus and fetlock were 181-182 degrees and 199-206 degrees, respectively. Peak vertical forces on the heel occurred at or near maximum extension of the carpal and fetlock joints. Peak forces on the toe occurred during flexion of the fetlock joint and at mean hoof angles of 28-31 degrees from the horizontal. The mean angles of the hoof from the horizontal at the time of heel contact were 6-7 degrees. Hoof lift occurred at mean carpal angles of 173-174 degrees and mean fetlock angles of 199-200 degrees. |
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Department of Veterinary and Comparative Anatomy, Pharmacology and Physiology, College of Veterinary Medicine, Washington State University, Pullman 99164-6520 |
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0001-5180 |
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PMID:8470468 |
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refbase @ user @ |
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1945 |
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Author |
Mellor, P.S. |
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Title |
African horse sickness: transmission and epidemiology |
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1993 |
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Veterinary Research |
Abbreviated Journal |
Vet Res |
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24 |
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2 |
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199-212 |
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Africa, Northern/epidemiology; African Horse Sickness/epidemiology/*transmission; African horse sickness virus/*physiology; Animals; Arachnid Vectors/microbiology; Ceratopogonidae/*microbiology; Culicidae/microbiology; Horses; Insect Vectors/*microbiology; Portugal/epidemiology; Spain/epidemiology; Ticks/microbiology |
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African horse sickness (AHS) virus causes a non-contagious, infectious, arthropod-borne disease of equines and occasionally of dogs. The virus is widely distributed across sub-Saharan African where it is transmitted between susceptible vertebrate hosts by the vectors. These are usually considered to be species of Culicoides biting midges but mosquitoes and/or ticks may also be involved to a greater or lesser extent. Periodically the virus makes excursions beyond its sub-Saharan enzootic zones but until recently does not appear to have been able to maintain itself outside these areas for more than 2-3 consecutive years at most. This is probably due to a number of factors including the apparent absence of a long term vertebrate reservoir, the prevalence and seasonal incidence of the vectors and the efficiency of control measures (vaccination and vector abatement). The recent AHS epizootics in Iberia and N Africa spanning as they do, 5 or more yr, seem to have established a new pattern in AHS virus persistence. This is probably linked to the continuous presence of adult C imicola in the area. Culicoides imicola is basically an Afro-Asiatic insect and prefers warm climates. Therefore its continuous adult presence in parts of Iberia and N Africa may be due to some recent moderations of the climate in these areas. |
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Institute for Animal Health, Pirbright Laboratory, Woking, Surrey, UK |
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0928-4249 |
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PMID:8102076 |
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Equine Behaviour @ team @ |
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2359 |
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Clayton, H.M. |
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Title |
The extended canter: a comparison of some kinematic variables in horses trained for dressage and for racing |
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Journal Article |
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Year |
1993 |
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Acta Anatomica |
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Acta Anat (Basel) |
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146 |
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2-3 |
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183-187 |
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Animal Husbandry; Animals; *Gait; Horses/*physiology; *Physical Conditioning, Animal; *Sports |
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This study was designed to test the hypothesis that there is no significant difference in selected temporal and linear stride variables of the extended canter in horses bred and trained for dressage or racing. Nine advanced-level dressage horses and 7 Thoroughbred racehorses were filmed at a frame rate of 200 Hz at an extended canter on a sand track. Two strides were recorded per trial, and each horse performed 6 or 7 trials. Temporal and linear data were determined from the films, and descriptive statistics (mean, SD) were calculated. Strides were selected for analysis on the basis of having a velocity in the range of 6.0-7.0 m/s, and multivariate analysis of variance was used to detect significant differences in the stride kinematics of horses trained for the two sports (p < or = 0.01). The average velocity of the dressage horses was 6.37 m/s, compared with 6.40 m/s for the racehorses. There were no significant differences between the two groups in velocity, stride duration, stride length or the distances between limb placements. The stance durations of all four limbs and the overlaps between them were longer, whereas the duration of the suspension phase was shorter in the dressage horses than in the racehorses (p < or = 0.01). The time between impacts of the diagonal limb pair was close to zero in both groups, with individual horses showing some variability in the order of placement of the diagonal limb pair. However, the sequence of footfalls was not significantly different between the two groups (p < or = 0.01). |
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Department of Veterinary Anatomy, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Canada |
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0001-5180 |
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PMID:8470464 |
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Equine Behaviour @ team @ |
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3751 |
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