Tuesday, September 9, 2025

Prehistoric Brains After Trauma: Could Dinosaurs Have Had Mental Disorders?

When we imagine dinosaurs, we picture thunderous hunters and herds of armored giants, instinctive, unstoppable, alien in their otherness. But beneath those ancient scales were brains shaped by the same evolutionary pressures that still mold animal minds today: fear, excitement, competition, and survival. What if we could peer past the fossilized bone into the neurobiological logic that governed a tyrannosaur’s behavior under stress? What if, like mammals and birds, dinosaurs possessed ancient neural circuits tuned to adversity, that recalibrated perception, emotion, and behavior in ways that echo what we now call mental disorders?

A dinosaur in a prison

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This blog entry explores the provocative idea that traits like impulsivity, hyper-vigilance, and even cognitive rigidity, hallmarks of conditions like anxiety, schizophrenia, depression, and PTSD, are not modern dysfunctions, but predictive adaptive responses: deeply conserved survival strategies honed across deep time. We will draw from the latest research in comparative neuroscience involving birds, reptiles and others, and consider behavioral shifts under chronic stress that mirror aspects of human psychopathology. By looking backward, through the lens of both paleontology and psychiatry, we might gain a clearer view not only of dinosaur behavior, but of the ancient, adaptive roots of our own minds.

Archosaurs and Their Living Legacy: The Key to Understanding Dinosaur Minds

To understand the minds of stressed dinosaurs, we start with a powerful evolutionary clue: dinosaurs were archosaurs, a group of reptiles that also includes modern birds and crocodilians. While the non-avian dinosaurs disappeared 66 million years ago, their lineage didn’t vanish, it branched and persisted, giving us rich comparative models to work with today. These two groups offer a remarkable contrast: birds are warm-blooded, highly social, and behaviorally flexible; crocodilians are cold-blooded, solitary, and behaviorally stereotyped, yet both exhibit complex learning, parental care, and powerful stress responses rooted in deep evolutionary history.

Beyond archosaurs, we can also draw meaningful comparisons from a broader set of vertebrates, fish, amphibians, and reptiles, to trace how animals adapt their brains and behavior in response to adversity. These comparisons let us triangulate what aspects of dinosaur neurobiology may have been ancestral, what was shared, and what may have been unique. By examining how modern animals cope with stress, through changes in vigilance, aggression, impulsivity, and cognitive flexibility, we can begin to piece together a picture of how dinosaurs, too, may have shifted into adaptive mental modes to survive harsh or unpredictable environments.

Stress in Birds and Reptiles: Ancient Roots of Emotional and Cognitive Shifts

While most studies of mental health and stress responses focus on mammals, compelling evidence from birds and reptiles suggests that adaptive emotional and behavioral changes under stress are deeply conserved across vertebrate evolution.

Birds

Birds, especially species like pigeons, crows, zebra finches, and chickens, have demonstrated striking parallels to mammals in how they respond to chronic or early-life stress:

  • Cognitive inflexibility: Stressed birds show reduced ability to shift strategies or adjust to new information, mirroring the rigidity seen in human conditions like anxiety, depression, and schizophrenia.
  • Impulsivity: Repeated exposure to stress in birds leads to riskier decision-making, impulsive feeding, and poor long-term planning, behavioral shifts that prioritize short-term survival over long-term optimization.
  • Vigilance and emotional reactivity: Chronically stressed birds exhibit exaggerated fear responses, heightened startle reactions, and avoidance behaviors, aligning with hyperarousal and anxiety.
  • Reduced neurogenesis and brain volume: Regions like the hippocampus, vital for learning and memory, shrink under chronic stress in birds, paralleling mammalian and human stress responses. The homologue of the mammal PFC is also affected by stress in ways like that in mammals.
  • Sensory filtering deficits: There is preliminary evidence that stress disrupts pre-attentive sensory gating in birds, similar to prepulse inhibition (PPI) deficits seen in schizophrenia and PTSD.

Reptiles

Though less studied, reptiles, such as lizards and turtles, also display conserved neuroendocrine responses to stress:

  • HPA-axis analog activation: Like mammals and birds, reptiles possess a hypothalamic-pituitary-adrenal system that releases glucocorticoids under stress. This hormonal cascade alters metabolism, behavior, and reactivity.
  • Behavioral withdrawal and freezing: Under stress, reptiles often reduce exploratory behavior, exhibit rigid threat postures, and favor freezing or defensive aggression, responses likely rooted in ancient survival strategies.
  • Memory and learning impairments: Chronic stress impairs spatial learning and reduces problem-solving flexibility in reptiles, particularly in geckos and turtles.
  • Epigenetic modulation: Some reptilian studies show that early developmental stress can cause lasting changes in gene expression, particularly in genes involved in neuroplasticity and hormone sensitivity.

Together, these findings suggest that adaptive behavioral and neurological responses to adversity, impulsivity, hypervigilance, reduced flexibility, and altered stress reactivity, are not limited to humans or even mammals. They appear in birds and reptiles too, pointing to an ancient, shared toolkit for coping with danger and uncertainty. If these traits emerge consistently in stressed modern archosaurs, it’s highly plausible that dinosaurs exhibited similar neurobehavioral shifts under environmental pressure. These may have served as temporary survival modes, reactive mental states tuned for hostile conditions, just like we see in modern animals today.

DSM Diagnoses That May Have Parallels In Dinosaurs

If you reframe “mental disorders” as context-dependent neuroecological strategies, then yes, Tyrannosaurs and other dinosaurs likely exhibited a full spectrum of stress-calibrated behavioral phenotypes. Not disorders in their world, but adaptive shifts in brain state, shaped by evolution. While we can’t diagnose extinct animals with DSM-5 categories, we can infer plausible analogs to human psychiatric traits.

Anxiety: Modern reptiles and birds show anxiety analogs like vigilance, avoidance, reduced foraging, and freezing when stressed. Dinosaurs almost certainly exhibited anxiety symptoms, some more than others, across a continuum.

Depression: In mammals, birds, reptiles, and fish, chronic stress, social defeat, or loss can lead to anhedonia (loss of pleasure-seeking), lethargy or reduced exploration, social withdrawal, as well as appetite and sleep changes. While we can't measure “sadness” in a T. rex, we can infer that low-dominance individuals or those in harsh ecological niches may have displayed reduced foraging, passivity, or increased vulnerability, the functional equivalents of depressive states.

PTSD: If a juvenile T. rex experienced prolonged early-life stress, their perceptual systems might have over-prioritized threat signals, resulting in false positives, exaggerated reactions, or preemptive aggression. This is functionally similar to paranoia or hyperarousal in PTSD.

OCD: Some dinosaurs could have exhibited repetitive ritualized patterns that stemmed from compulsions. Compulsive behaviors could have led to stereotypies such as pacing, repetitive head bobbing, overgrooming, or self-mutilation. These are common in modern zoo animals, birds in cages, and reptiles in tanks, especially under boredom or stress.

Autism: Some social dinosaur species may have had members with limited sociality, with strong solitary focus, low social interest, repetitive behaviors, or reduced communication and this might not have been maladaptive. These may have represented natural variation, helping them to focus on food and survival rather than fraternizing and this impaired social perception might have led to fitness in certain environments.

ADHD: Hyperactivity and novelty seeking could have been adaptive in certain niches leading to impulsivity, roaming, inattention, and erratic exploration. Birds, reptiles, and even fish show dopaminergic disinhibition after chronic stress.

Bipolar: Some members of a dinosaur species could have cycled from depression to a form of mania. This may have been adaptive because it helped them swing from resting in oppressive times to fully taking advantage of beneficial circumstances.

Psychopathy: In rough, traumatic settings predatory aggression and low affiliative bonding could have led to adaptive lack of fear, goal-driven behavior that was non-pathological in context. This could have surfaced as erratic attack behavior, risk-taking, boundary violations, and territorial overexpansion. Stress-altered dopaminergic systems are linked to impulsivity in birds, mammals, and fish.

We can also imagine that dinosaurs could have had panic disorder, startle hyperreactivity, sleep disorders, attachment disorders, and social anxiety. If dinosaurs had rich, plastic brains, as their descendants do, then they almost certainly experienced state shifts we now pathologize in humans. Dinosaurs likely had a wide behavioral range, and under chronic stress or developmental trauma, that range probably skewed toward survival-prioritized mental modes. These behaviors were not "disorders" in their context, but reactive calibrations of the brain, conserved across deep time. The full catalog of dinosaur mental states remains speculative, but the building blocks of modern disorders were almost certainly present.

The Benefits of Cognitive Inflexibility in Response to Stress

Stress reshapes learning and cognition in birds along several interacting axes: timing, intensity, and social context. Acute stressors can sometimes sharpen vigilance and speed up threat learning, but repeated or unpredictable stress tends to tax the HPA axis, elevate corticosterone over longer windows, and push cognition toward faster, noisier strategies.

Song learning is one of the clearest windows into these effects. In species with sensitive periods, stress during tutoring or practice narrows the repertoire, reduces motif accuracy, and increases variability from rendition to rendition. Neuroanatomically, stress perturbs the development and plasticity of nuclei such as HVC and RA and the basal-ganglia–like Area X, where dopaminergic signals normally calibrate error-based refinement; disrupted dopamine and reduced BDNF signaling can degrade the precision of auditory–motor matching. Adults that were stressed as juveniles often carry these fingerprints forward: they are slower to adjust song after auditory feedback manipulations, less able to acquire new syllables, and less consistent in performance when challenged.

Memory systems are similarly tuned. The hippocampus in food-caching and scatter-hoarding birds supports high-resolution spatial memory and shows adult neurogenesis; chronic or early corticosterone exposure reduces neurogenesis, dendritic complexity, and long-term potentiation, yielding poorer cache recovery and less flexible route choice. In decision-making tasks, stressed individuals show more perseveration and slower reversal when contingencies flip, essentially a reduction in cognitive flexibility, while at the same time showing quicker acquisition of simple avoidance responses, an asymmetry that reflects the well-known inverted-U relation between arousal and learning.

Attention and learning style also reconfigure. Under stress, juveniles become more neophilic in some contexts (sampling new foods and sites more readily) yet more neophobic in others (warier of handlers, novel objects, or traps), reflecting a reallocation of attention toward cues that best predict immediate survival. In judgment-bias paradigms, birds exposed to chronic stress interpret ambiguous cues more pessimistically, which can dampen exploration and learning from partial feedback.

These cognitive changes are mediated not only by circulating hormones but also by lasting molecular marks. Early adversity can alter glucocorticoid receptor expression and epigenetic regulation in brain regions supporting learning, biasing later stress reactivity and plasticity. This makes these changes look like predictive adaptive responses. Mothers can transmit some of this tuning before hatch via yolk hormones, effectively “pre-setting” offspring for expected environmental volatility. The result is a developmental program that trades fine-grained accuracy and tutor fidelity for independence, rapid sampling, and broad social learning when parental care is unreliable.

Chronic stress in humans leads to similar changes in higher-order brain states that can reduce activity in the PFC and hippocampus (the stress cascade), causing executive deficits and mental inflexibility. I have previously written about how this may have been adaptive in nature (Reser, 2016; 2007). I believe cognitive inflexibility can enhance survival in highly constrained, high-threat environments by favoring reliability, predictability, and resistance to distraction over exploratory flexibility. In other words, in dangerous or unpredictable settings, the cost of being wrong or of switching strategies too easily can be much greater than the cost of being rigid.

Sticking to a narrow set of well-practiced defensive behaviors (e.g. freezing, fleeing, hiding, aggression) may be more reliable than deliberation. In flexible cognition, ambiguity is tolerable; in defensive states, it’s dangerous. Inflexibility reduces hesitation. In abusive environments, seeking novelty or shifting strategies might repeatedly backfire. Cognitive rigidity helps avoid exploration-exploitation errors, keeping an individual locked into “safe” (even if suboptimal) routines. It may have helped animals not get stuck in overthinking or analysis paralysis so that they could simplify things and focus on survival. Essentially, it may have been a heuristic compression strategy under duress. Fascinatingly chronic stress often impairs song learning in songbirds, leading to simpler repertoires or less accurate mimicry. Stress-exposed birds may also shift from careful, attention-based learning to faster, riskier trial-and-error strategies.

When the environment is hostile, chaotic, or resource-poor, spending time evaluating options or mentally simulating outcomes may become a liability. Cognitive inflexibility strips away nuance in favor of quick threat classification (“friend or foe,” “safe or unsafe”), actionable routines over deliberation, and hyper-salient cues over ambiguous signals. In that sense, it’s not just about freezing out complexity, it’s about optimizing the brain for immediate survival rather than long-term gain. You’re simplifying the model of the world to minimize uncertainty, even if that means overestimating threat or underutilizing social opportunity. There’s a strong parallel here with defensive downshifts in perception and cognition across species, like prey animals who reduce exploratory foraging when they smell a predator. Flexibility is a luxury of safety. In this context, schizophrenia-like features such as vigilance, rigidity, and emotional reactivity become a tightly integrated “defense set” that may play a role in most tetrapod vertebrates. This makes me wonder if T. Rex had a brain state comparable with schizophrenia.

In a chronically threatening world, a simpler, more rigid mind may be better tuned to survive. “When the world’s on fire, don’t process, pattern-match and act.” And it scales: from rodents freezing at a twig snap, to humans forming fast heuristics like “everyone’s out to get me” after prolonged adversity. It's not accurate, but it’s efficient, predictive, and in some contexts, life-saving. You might even define schizophrenia not as cognitive breakdown, but as the overactivation of a compressed defensive schema, built for ancestral threat, miscalibrated for modern peace. I imagine dinosaurs could have found use in this inflexibility sometimes too.

Tyrannosaurus Rex as a Case In Point

The brain size of Tyranosaurus Rex makes it interesting for the present discussion. T. rex had the largest brain of any dinosaur. In fact, its brain was nearly twice the size of any other dino. It measured around 300 cubic centimeters, placing it around the size of a chimpanzee brain (380 cc) but far smaller than a human’s 1,300 cc. For its time though, it was colossal, especially when compared to the velociraptor’s 15cc brain or the gargantuan dreadnaughtus’ 25cc brain. The T Rex cerebrum would likely have had some cognitive flexibility, adequate for learned routines, territory, and hunting strategies. The brain-to-body ratio (EQ) was small compared to mammals, and many theropod dinosaurs have larger EQs than T Rex, suggesting energy-efficient, heuristic processing, consistent with reactive, low-plasticity cognition. But in the Cretaceous, and all the time that came before it, T Rex may have been one of the smartest animals around. And this might mean that it had much to benefit from downplaying high-level cognition during hostile times. Did stress turn it into an even more savage tyrant king?

Tyrannosaurus rex, like modern mammals and birds, likely possessed an adversity-calibrated neurobehavioral system that could shift individuals toward a “reactive defense phenotype” under chronic environmental stress. This phenotype could have favored heightened vigilance, cognitive rigidity, and impulsive aggression. In T. rex, early-life stress (e.g. poor food availability, high parental competition) likely led to suppressed hippocampal development, prefrontal-like downregulation, and upregulated amygdaloid/defensive circuitry. Juvenile tyrannosaurs exposed to chronic stress may have developed rigid, antisocial behavioral patterns. Delusional-like perceptual misfires are harder to prove, but oversensitivity to ambiguous stimuli (false positives) could have helped avoid ambush or surprise in a volatile ecosystem. Just like a stressed rodent shows prepulse inhibition deficits, a stressed T. rex might have been easily startled, overly reactive, or “trigger-happy” in its threat detection system, trading false alarms for survival.

As we discussed, chronic corticosterone exposure in birds is known to reduce neurogenesis, increase impulsivity, impair spatial memory, and suppress social behavior. As in humans, these are brought forth through epigenetic modifications (e.g., DNA methylation, histone acetylation) in response to environmental stress. Modern birds exposed to prenatal stress develop smaller brains, reduced sociability, slower learning, and heightened reactivity because of these changes.

Stressed adult birds may reduce investment in parental care, feeding chicks less often, abandoning nests more readily, or investing in fewer offspring overall. In response, early life stress in youg birds often reduces birds responsiveness to parental cues while increasing their attention to unrelated birds of the same species (conspecifics). This shift likely reflects an adaptive strategy, helping juveniles learn from peers and integrate into broader social groups when parental care is unreliable. Experiments in species like zebra finches and starlings confirm that stressed chicks attend less to parents and more to non-kin, accelerating independence. Could this have been a strategy also used by dinosaurs like tyrannosaurs?

How closely related was T rex to birds? Tyrannosaurus rex, like all birds, was a member of the Theropoda, a group of bipedal, mostly carnivorous dinosaurs. Both T. rex and modern birds even belong to a more specialized branch called Coelurosauria, which includes feathered dinosaurs and some of the most cognitively advanced species of the Mesozoic. This makes me feel pretty confident about drawing parallels between birds and Tyrannosaurus. Although it is important to mention that they would have shared a pretty ancient common ancestor. The ancestor of all birds lived around 100 million years ago and the common ancestor that bird shared with the T Rex would have lived 160 million years ago, that leaves lots of time for genetic changes in the way the brain responds to stress.

Conclusion

By studying dinosaur’s closest living relatives, birds and crocodilians, and by examining how stress alters the brains and behaviors of animals across the tree of life, we can begin to build a scientifically grounded picture of how dinosaurs may have responded to adversity. The evidence is clear: chronic stress in birds and reptiles can lead to heightened vigilance, impulsivity, emotional reactivity, and cognitive inflexibility, traits long associated with human mental disorders like anxiety, depression, and schizophrenia. But in nature, these traits often represent adaptive strategies, not pathologies. They reflect survival-oriented recalibrations, predictive shifts that prioritize defense, alertness, and short-term action in the face of threat or instability.

If such responses are found in birds, lizards, and mammals alike, it is reasonable to infer that dinosaurs also possessed ancient neural systems capable of mounting similar behavioral and physiological shifts. In this light, what we label as "mental disorders" in humans may reflect a shared evolutionary toolkit: a repertoire of adaptive responses, once sculpted by danger and deprivation, now mismatched with the modern world.

References:

Reser, J. 2016. Chronic stress, cortical plasticity and neuroecology. Behavioural Processes. 129:105-115.

Reser, J. 2007. Schizophrenia and phenotypic plasticity: Schizophrenia may represent a predicitive, adaptive response to severe environmental adversity that allows both bioenergetic thrift and a defensive behavioral strategy. Medical Hypotheses, Volume 69, Issue 2, 383-394.

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