75 research outputs found

    Mirror on the wall, who is the horsest of our all? Self-recognition in Equus caballus

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    Mirror Self-Recognition (MSR) is an extremely rare capacity in the animal kingdom that reveals the emergence of complex cognitive capacities (de Waal 2008). So far, MSR has been reported only in humans, chimpanzees (Gallup, 1970), bottlenose dolphins (Reiss and Marino, 2001) and Asian elephants (Plotnik et al, 2006), all species characterized by a highly developed cognition. There is growing evidence that domestic horses posses high cognitive abilities, such as crossmodal individual recognition (Proops et al, 2009), triadic post-conflict reunion to maintain social homeostasis (Cozzi et al, 2010), complex communicative systems (Whatan and McComb, 2014), flexibility in problem-solving (Lovrovich et al, 2015), and long-term memory (Hanggi and Ingersoll, 2009). All these capacities make horses a good candidate to test the ability of MSR in a domestic species. Through a classical MSR experimental paradigm (de Waal 2008) we tested eight horses living in social groups under semi-natural conditions (from the Italian Horse Protection rescue centre). Animals showing MSR typically go through four stages (Plotnik et al, 2006): (i) social response, (ii) physical mirror inspection (e.g., looking behind the mirror), (iii) repetitive mirror-testing behaviour (i.e., the beginning of mirror understanding), and (iv) selfdirected behaviour (i.e., recognition of the mirror image as self). The final stage, known as the “mark-test”, is verified when a subject spontaneously uses the mirror to check for a coloured artificial mark on its own body which it cannot perceive otherwise. The horses underwent through a three-phase “mark-test”: 1) with sham mark (transparent ultrasound water gel) positioned on both side at jaw level, 2) mark (yellow eye shadow mixed with ultrasound water gel) positioned on left side of jaw (with sham mark on the right), 3) mark (yellow eye shadow mixed with ultrasound water gel) positioned on right side of jaw (with sham mark on the left) The mirror was one 0.5-cm-thick pieces of 140x220-cm plexiglass glue on wood. Each test lasted one hour, horses were tested once a day, in consecutive days and at the same time. Our preliminary result on 1 horse shows some changes in self-directed behaviours which can be attributed to presence of the coloured mark. Firstly, the presence of the coloured marked significantly increased the frequency of scratching on both sides of the muzzle (p < 0.0001). The most intriguing result (p < 0.0001) comes from the comparison of the scratching rates directed towards the coloured mark side (N = 41) and the sham mark side (N = 23). Under the control condition (i.e. sham mark on both sides) no statistical difference was found for the scratching rates directed to the muzzle sides (dx N = 8; sx N = 5). Although further analyses are needed to confirm these preliminary results, our finding opens new scenarios about the evolution of Mirror Self-Recognition. The capacity of horses to recognize themselves in a mirror may be the outcome of an evolutionary convergence process driven by the cognitive pressures imposed by a complex social system and maintained despite thousands years of domestication

    Are horses capable of mirror self-recognition? A pilot study

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    Mirror Self-Recognition (MSR) unveils complex cognitive, social and emotional skills and it has been found only in humans and few other species, such as great apes, dolphins, elephants and magpies. In this pilot study, we tested if horses show the capacity of MSR. Four subjects living socially under naturalistic conditions were selected for the experiment. We adopted the classical mark test, which consists in placing a coloured mark on an out-of-view body part, visible only through mirror inspection. If the animal considers the image as its own, it will use its reflection to detect the mark and will try to explore it. We enhanced the classical paradigm by introducing a double-check control. Only in the presence of the reflecting surface, animals performed tactile and olfactory exploration of the mirror and looked behind it. These behaviors suggest that subjects were trying to associate multiple sensory cues (visual, tactile and olfactory) to the image in the mirror. The lack of correspondence between the collected stimuli in front of the mirror and the response to the colored mark lead us to affirm that horses are able to perceive that the reflected image is incongruent when compared with the memorized information of a real horse. However, without replication of data, the self-directed behavior towards the colored marks showed by our horses cannot be sufficient per se to affirm that horses are capable of self-recognition

    Brief note about plasma catecholamines kinetics and submaximal exercise in untrained standardbreds

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    Four untrained standardbred horses performed a standardized exercise test on the treadmill and an automated blood collection system programmed to obtain blood samples every 15 s was used for blood collection in order to evaluate the kinetics of adrenaline and noradrenaline. The highest average values obtained for adrenaline and noradrenaline were 15.0 +/- 3.0 and 15.8 +/- 2.8 nmol/l respectively, with exponential accumulation of adrenaline (r = 0.977) and noradrenaline (r = 0.976) during the test. Analysis of the correlation between noradrenaline and adrenaline for each phase of the test shows that correlation coefficient decreases as the intensity of exercise increases (from r = 0.909 to r = 0.788). This suggests that during submaximal exercise, the process for release, distribution and clearance of adrenaline into blood circulation differs from that of noradrenaline

    Rein Tension Signals Elicit Different Behavioral Responses When Comparing Bitted Bridle and Halter

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    When a rider maintains contact on the reins, rein tension will vary continuously in synchronicity with the horse's gait and stride. This continuous variation makes it difficult to isolate the rein tension variations that represent a rein tension signal, complicating interpretation of rein tension data from the perspective of horse-rider interaction. This study investigated (1) the characteristics of a rein tension signal and (2) horse response to a rein tension signal for backing, comparing pressure applied by a bit (bridle), or by a noseband (halter). Twenty Warmblood horses (10 young, 10 adult) wearing a rein tension meter were trained to step back in the aisle of a stable. The handler stood next to the horse's withers, applying tension on the reins until the horse stepped back. This was repeated eight times with the bridle and eight times with the halter. Data analysis was performed using mixed linear and logistic regression models. Horses displaying behaviors other than backing showed significantly increased response latency and rein tension. Inattentive behavior was significantly more common in the halter treatment and in young horses, compared with the bridle treatment and adult horses. Evasive behaviors with the head, neck, and mouth were significantly more common in the bridle treatment than in the halter treatment and the occurrence of head/neck/mouth behaviors increased with increasing rein tension and duration of the rein tension signal. When controlling for behavior, the horses responded significantly faster and to a lighter rein tension signal in the bridle treatment than in the halter treatment. By scrutinizing data on rein tension signals in relation to horse behavior and training exercise, more can be learnt about the horse's experience of the pressures applied and the timing of the release. This can assist in developing ways to evaluate rein tension in relation to correct use of negative reinforcement

    Inter- and intra-species communication of emotion: chemosignals as the neglected mediumi

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    Human body odors contain chemosignals that make species-specific communication possible. Such communication is without communicative intent and is generally below the threshold of consciousness. Human recipients of these chemosignals produced during emotional conditions display a simulacrum of the emotional state under which the chemosignal was produced. The investigation of an inter-species transfer of emotions via chemosignals was initiated by considerations of the historically anchored interdependence between humans and domesticated species, such as dogs and horses. Indeed, experiments with dogs have demonstrated that human body odors produced under emotional conditions of happiness and fear led dogs to manifest corresponding emotions to those experienced by humans. Preliminary data from horses also show that human body odors collected under fear and happiness conditions activate the autonomic nervous system of horses differentially. These studies indicate the possibility of a road to open our understanding of inter-species emotional communication via chemosignals.info:eu-repo/semantics/publishedVersio

    Economic consequences of investing in anti-HCV antiviral treatment from the Italian NHS perspective : a real-world-based analysis of PITER data

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    OBJECTIVE: We estimated the cost consequence of Italian National Health System (NHS) investment in direct-acting antiviral (DAA) therapy according to hepatitis C virus (HCV) treatment access policies in Italy. METHODS: A multistate, 20-year time horizon Markov model of HCV liver disease progression was developed. Fibrosis stage, age and genotype distributions were derived from the Italian Platform for the Study of Viral Hepatitis Therapies (PITER) cohort. The treatment efficacy, disease progression probabilities and direct costs in each health state were obtained from the literature. The break-even point in time (BPT) was defined as the period of time required for the cumulative costs saved to recover the Italian NHS investment in DAA treatment. Three different PITER enrolment periods, which covered the full DAA access evolution in Italy, were considered. RESULTS: The disease stages of 2657 patients who consecutively underwent DAA therapy from January 2015 to December 2017 at 30 PITER clinical centres were standardized for 1000 patients. The investment in DAAs was considered to equal €25 million, €15 million, and €9 million in 2015, 2016, and 2017, respectively. For patients treated in 2015, the BPT was not achieved, because of the disease severity of the treated patients and high DAA prices. For 2016 and 2017, the estimated BPTs were 6.6 and 6.2 years, respectively. The total cost savings after 20 years were €50.13 and €55.50 million for 1000 patients treated in 2016 and 2017, respectively. CONCLUSIONS: This study may be a useful tool for public decision makers to understand how HCV clinical and epidemiological profiles influence the economic burden of HCV

    Cavalli allo specchio. Viaggio nella mente dei cavalli per conoscerli, addestrarli e gestirli in scuderia

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    La mente del cavallo controlla il suo comportamento con gli stessi meccanismi psicologici degli altri animali e dell’essere umano. Se anche spesso si sente parlare di “arte dell’equitazione”, non possiamo ignorare che il comportamento, la psicologia e l’etologia del cavallo sono scienza a tutti gli effetti. La relazione che abbiamo instaurato con quest’animale presenta evidenti criticità, dovute alla mancata conoscenza dei meccanismi della mente che ne regolano il comportamento. Avere accesso e poter comprendere le nozioni scientifiche di tali meccanismi, permetterà a professionisti o semplici appassionati di instaurare un canale di comunicazione efficace ed efficiente con il proprio cavallo. Solo così sarà possibile avere cavalli tranquilli, che si sentono sicuri ad averci accanto, e questo garantirà il loro benessere psichico e il miglioramento delle performance in gara o durante una bella passeggiata

    A rein tension signal can be reduced by half in a single training session

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    Rein tension signals are, in essence, pressures applied on the horse's mouth or nose, via the bit/noseband, by a rider or trainer. These pressures may feel uncomfortable or even painful to the horse and therefore it is important to reduce rein tension magnitude to a minimum. The aim of this study was to investigate the magnitude of a rein tension signal for backing up, using negative reinforcement. We wanted to assess how much the magnitude of rein tension could be reduced over eight trials and if the learning process would differ depending on headstall (bridle/halter). Twenty Warmblood horses were trained to step back from a rein tension signal with the handler standing next to the horse, holding the hands above the horse's withers. As soon as the horses stepped back, rein tension was released. The horses were either trained with a bridle first (first treatment, eight trials) and then with a halter (second treatment, eight trials), or vice versa in a cross-over design. All horses wore a rein tension meter and behavior was recorded from video. The sum of left and right maximum rein tension from onset of the rein tension signal to onset of backing (signaling rein tension) was determined for each trial. Mixed linear and logistic regression models were used for the data analysis. In both treatments, signaling rein tension was significantly lower in trial 7-8 than the first trial (p < 0.02). Likewise, signaling rein tension was significantly lower (p < 0.01), and the horses responded significantly faster, (p < 0.001) in the second treatment compared to the first, regardless of headstall. The maximum rein tension was reduced from 35 N to 17 N for bridle (sum of left and right rein) and from 25 N to 15 N for halter in the first eight trials. Rein tension was then further reduced to 10 N for both bridle and halter over the eight additional trials in the second treatment, i.e. to approximately 5 N in each rein. There was no significant difference in learning performance depending on headstall, but the bitted bridle was associated with significantly more head/neck/mouth behaviors. These results suggest that it is possible to reduce maximum rein tension by half in just eight trials. The findings demonstrate how quickly the horse can be taught to respond to progressively lower magnitudes of rein tension through the correct application of negative reinforcement, suggesting possibilities for substantial improvement of equine welfare during training
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