Lester O'brien’s scientific contributions

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Publications (2)


Continuing challenges of elephant captivity: the captive environment, health issues, and welfare implications
  • Article
  • Full-text available

September 2024

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241 Reads

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1 Citation

Catherine Doyle

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Lester O'brien

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[...]

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Although the well-being of elephants in captivity is of paramount importance, the confinement of these long-lived, highly intelligent, and socially complex animals continues to present significant challenges. Here, we provide an overview of the current state of elephant confinement (primarily in the West) by examining captive facilities, improvements, and continuing problems, and the clinical/behavioral/ neural issues that remain. Specifically, we examine quantitative and qualitative aspects of the enclosed space, sociocognitive factors, dietary differences, and health/ welfare concerns (e.g., stereotypies, physical health, nutrition, reproduction, life expectancy). The challenges of the captive environment become especially salient when juxtaposed next to the complex, multifaceted characteristics of the elephant's natural environment. Despite the best efforts of some facilities to improve the captive environment, serious welfare challenges remain. Such confinement issues thus raise important welfare and ethical concerns with regards to captive elephant well-being.

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Midsagittal sections of the African elephant (Loxodonta a fricana), bottlenose dolphin (Tursiops truncatus), human (Homo sapiens), and rat (Rattus norvegicus) brains.
Included are tracings of superficial pyramidal neurons from the neocortex of each species. Note that the anterior portion of the frontal lobe has been removed from the dolphin brain. Traced neurons are reproduced from previous studies on quantitative neuromorphology: African elephant (Jacobs et al. 2011), bottlenose dolphin (Butti et al. 2015), human (Jacobs et al. 2018; Warling et al. 2020), and rat (Jacobs et al. 2018). Elephant brain image courtesy of Dr. Paul Manger, University of Witwatersrand, Johannesburg, South Africa. Dolphin brain image courtesy of Drs. Bruno Cozzi and Ksenia Orekhova, University of Padova, Padua, Italy. Abbreviations: Ca, caudate; Cb, cerebellum; CC, corpus callosum; Cereb, cerebral cortex; H, hypothalamus; M, medulla; Mid, midbrain; P, pons; Th, thalamus.
Different levels of the cerebral cortex affected by impoverished (captive) and enriched (natural) environments.
In impoverished/captive environments, there are several cortical changes: (a) Decreases in cortical thickness, (b) smaller capillary diameter, (c) decreases in neuronal soma size and fewer glial cells per neuron, (d) less complex dendritic branching, (e) fewer dendritic spines, and (f) less efficient synapses. Image courtesy of Dr. Arnold B. Scheibel.
Schematic of hypothalamic–pituitary–adrenal (HPA) axis activation.
Coronal sections of the African elephant, bottlenose dolphin, human, and rat brains revealing major structures involved in the neural response to stress following hypothalamic–pituitary–adrenal (HPA) axis activation and the release of glucocorticoids (black arrows) from the adrenal cortex. A simplified schematic illustrates the basic structures and connections within this circuitry. Structures in the schematic are color coded to match brain cross sections—note that the medial prefrontal cortex (PFC) and the bed nucleus of the stria terminalis (BNST) are not visible in cross-sections. In addition, the entire hypothalamus is illustrated in the cross-sections rather than just the paraventricular nucleus (PVN). Major excitatory (red arrows) and inhibitory (blue arrows) projections are shown. In general, the amygdala and associated circuitry provide a positive feedback loop to activate the HPA axis whereas the hippocampus and associated circuitry contribute to a negative feedback loop to reduce HPA activity. Although not shown in the schematic, the anterior BNST tends to increase HPA axis activity whereas the posterior division tends to inhibit it (Ch’ng et al. 2018). Also represented are three types of neurons and their response to chronic stress: (1) Stellate neurons in the (basolateral) amygdala, which tend to increase dendritic extent; (2) cortical pyramidal neurons in the medial PFC, which show reductions in apical dendritic extent; and (3) CA3 pyramidal neurons in the hippocampus, which undergo degeneration of the apical dendrite.
Schematic of brain structures involved in behavioral stereotypies.
Horizontal sections of African elephant and bottlenose dolphin brains, and coronal sections of human and rat brains revealing major structures involved in behavioral stereotypies. Not all structures are visible in all cross sections except for the human brain. A simplified schematic illustrates basic GABAergic, glutamatergic, and dopaminergic connections within this circuitry. Structures in the schematic are color coded to match brain cross sections. The direct pathway includes the following structures/projections: motor cortical areas → striatum → globus pallidus (interna)/substantia nigra (pars reticulata) → ventral anterior and ventral lateral nuclei of the thalamus → motor cortical areas. The structures of the indirect pathway are similar to those in the direct pathway with the addition of the subthalamic nucleus: motor cortical areas → striatum → globus pallidus (externa) → subthalamic nucleus→ globus pallidus (interna)/substantia nigra (pars reticulata) → ventral anterior and ventral lateral nuclei of the thalamus → motor cortical areas (Calabresi et al. 2014; Langen et al. 2011b; Lewis et al. 2006). Abbreviations: D 1 and D 2, dopamine receptors; GPe, globus pallidus externa; GPi, globus pallidus interna; SNpc, substantia nigra pars compacta; SNpr, substantia nigra pars reticulata; STN, subthalamic nucleus. Schematic is adapted from Gao and Singer (2013).
Putative neural consequences of captivity for elephants and cetaceans

September 2021

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808 Reads

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20 Citations

The present review assesses the potential neural impact of impoverished, captive environments on large-brained mammals, with a focus on elephants and cetaceans. These species share several characteristics, including being large, wide-ranging, long-lived, cognitively sophisticated, highly social, and large-brained mammals. Although the impact of the captive environment on physical and behavioral health has been well-documented, relatively little attention has been paid to the brain itself. Here, we explore the potential neural consequences of living in captive environments, with a focus on three levels: (1) The effects of environmental impoverishment/enrichment on the brain, emphasizing the negative neural consequences of the captive/impoverished environment; (2) the neural consequences of stress on the brain, with an emphasis on corticolimbic structures; and (3) the neural underpinnings of stereotypies, often observed in captive animals, underscoring dysregulation of the basal ganglia and associated circuitry. To this end, we provide a substantive hypothesis about the negative impact of captivity on the brains of large mammals (e.g., cetaceans and elephants) and how these neural consequences are related to documented evidence for compromised physical and psychological well-being.

Citations (1)


... Although the direct impact of FTS on spatial memory has not been established, the associated neural degeneration could potentially affect broader neurological functions. Additionally, captivity has been associated with neural changes in elephants, including reduced hippocampal activity and behavioural abnormalities, likely due to environmental deprivation and chronic stress [24]. These findings underscore the importance of environmental enrichment and appropriate social structures in maintaining neural health. ...

Reference:

Memory-Based Navigation in Elephants: Implications for Survival Strategies and Conservation
Putative neural consequences of captivity for elephants and cetaceans