Preliminary investigation of the effects of a concert on the behavior of zoo animals.

To increase visitor footfall and engagement, zoos may host public events that may extend outside typical opening hours. With plans to hold a 2-day concert at Tayto Park, Ireland, this study aimed to identify the behavioral response to the music event of a selected group of species in the zoo. Twenty-two species were observed across three phases of the event (pre-, during, and post event). Specific behaviors of interest were categorized as active, resting, asleep, abnormal, and out of sight, with repeated observations being made at each enclosure during each phase. Alongside these behavioral data, sound pressure levels (SPLs) were concurrently recorded at the observation locations in terms of both dB(A) and dB(C). The median dB(C) levels during the event were found to be significantly higher (mdn = 64.5 dB) when compared with both pre-event (mdn = 60.7 dB) and postevent phases (mdn = 59.4 dB), while dB(A) levels were only significantly higher during the event (51.7 dB) when compared with the pre-event phase (mdn = 49.8 dB). We found some species-specific behavioral changes (mainly associated with active and resting behaviors) correlated with increased SPLs and/or event itself. However, the behavioral responses varied between species and there were numerous species that did not respond with any change in behavior to the increased SPLs or the event itself. This variation in response across species reinforces the need for monitoring of behavioral changes as well as consideration of their natural behavioral ecology when implementing appropriate mitigation strategies. Further research should be encouraged to provide an evidence-based assessment of how music events may affect animal welfare and behavior and to test the efficacy of mitigation strategies that are implemented to safeguard animal welfare.

Modeling the effects of muscle contraction on the mechanical response and circumferential stability of coronary arteries.

Smooth muscle contraction regulates the size of the blood vessel lumen which directly affects the mechanical response of the vessel. Folding in arteries has been observed in arteries during excessive contraction, known as a coronary artery spasm. The interplay of muscle contraction, geometry, and material responses and their effects on stability can be understood through mathematical models. Here, we consider a three-layer cross-sectional model of a coronary artery with anisotropic properties and intimal thickening, and perform a linear stability analysis to investigate the circumferential folding patterns that emerge due to muscle contraction. Our model shows that a critical level of contractile activity yields a uniform strain distribution across the arterial wall. When the muscle is contracted above this critical level, the tissue behaves isotropically and it is more prone to circumferential instability. This theoretical framework could serve as a valuable tool to understand the relationship between arterial lumen morphology and wall contraction in health and disease.

Investigation of the efficacy of the GnRH agonist deslorelin in mitigating intraspecific aggression in captive male Amur leopards (Panthera pardus orientalis).

Housing bachelor groups is a necessary aspect of the care and husbandry of non-breeding individuals in zoological collections. Intraspecific aggressive behaviors may occur in this setting despite management strategies designed to mitigate these behaviors. Androgens (including testosterone) are associated with aggression in male species and interventional techniques to alter the animals' physiology to modify aggressive behavior are sometimes required. When agonistic behavior and physical aggression in two mature male Amur leopards housed together at Tayto Park escalated, despite all strategic management involvements, further intervention to moderate aggression was required. The gonadotropin-releasing hormone (GnRH) agonist, deslorelin, has been found to be effective in reducing androgens in domestic and non-domestic carnivores. We hypothesized that deslorelin's suppressive effect on hypothalamic-pituitary-gonadal axis would mitigate intraspecific aggression in two male intact leopards. Behavioral observations were carried out pre- and post-implant implantation of 9.4 mg deslorelin implant. The frequency of agonistic/aggressive behaviors for both leopards declined significantly (p < 0.05), as did marking behaviors post-implantation (p < 0.001). The insertion of deslorelin implants in two male intact leopards demonstrating increased frequency and severity of aggressive behaviors resulted in a reduction of the frequency of these behaviors. Deslorelin implantation should be considered for management of interspecific aggression of intact male leopards in bachelor groups.

Immunodetection of disease-associated mutant PrP, which accelerates disease in GSS transgenic mice.

The absence of infectivity-associated, protease-resistant prion protein (PrP(Sc)) in the brains of spontaneously sick transgenic (Tg) mice overexpressing PrP linked to Gerstmann-Sträussler Scheinker syndrome, and the failure of gene-targeted mice expressing such PrP to develop disease spontaneously, challenged the concept that mutant PrP expression led to spontaneous prion production. Here, we demonstrate that disease in overexpressor Tg mice is associated with accumulation of protease-sensitive aggregates of mutant PrP that can be immunoprecipitated by the PrP(Sc)-specific monoclonal antibody designated 15B3. Whereas Tg mice expressing multiple transgenes exhibited accelerated disease when inoculated with disease-associated mutant PrP, Tg mice expressing mutant PrP at low levels failed to develop disease either spontaneously or following inoculation. These studies indicate that inoculated mutant PrP from diseased mice promotes the aggregation and accumulation of pre-existing pathological forms of mutant PrP produced as a result of transgene overexpression. Thus, while pathological mutant PrP possesses a subset of PrP(Sc) characteristics, we now show that the attribute of prion transmission suggested by previous studies is more accurately characterized as disease acceleration.