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Default mode network

The default mode network (DMN) is a large-scale, intrinsic network characterized by coordinated activity among specific cortical and subcortical regions that increases during states of rest, , and internally focused , while deactivating during goal-directed, externally oriented tasks. This network, first systematically described in 2001, supports essential processes such as self-referential thinking, retrieval, future planning, and , thereby facilitating the brain's integration of personal experiences across time. Key anatomical components include the medial prefrontal cortex (mPFC), (PCC)/, (including the ), and medial temporal structures like the . The discovery of the DMN emerged from () studies in the early 2000s, where researchers observed consistent, task-induced deactivations in certain regions relative to a resting , revealing an organized "default" mode of function that persists without external demands. Subsequent advances in () confirmed these patterns through resting-state connectivity analyses, showing that DMN regions exhibit low-frequency fluctuations synchronized even in the absence of tasks. This shift in emphasized the 's intrinsic activity, which accounts for a significant portion of its —up to 60–80%—highlighting the DMN's role in ongoing internal mentation rather than just passive idling. Functionally, the DMN operates as a dynamic with subsystems specialized for distinct roles: subsystem (involving mPFC and ) handles self-referential and conceptual processing, while the dorsal medial subsystem supports social inference, and the medial temporal subsystem aids in and scene construction. It interacts reciprocally with task-positive networks, such as the multiple-demand network (involved in executive control) and the (which detects environmental relevance), enabling flexible shifts between introspective and attentive states—for instance, during narrative comprehension or moral decision-making. Disruptions in DMN integrity, such as reduced connectivity or hyperactivity, are implicated in neuropsychiatric conditions including (where posterior DMN hubs degenerate early), (linked to excessive rumination), and (associated with impaired self-other distinctions). Recent research has refined the DMN's architecture, revealing balanced connectivity across cortical types and that positions it at one end of a principal of macroscale brain function, opposing sensory-motor systems. These insights underscore the DMN's evolutionary significance for adaptive behaviors like prospection and , while opening avenues for targeted interventions in cognitive and emotional disorders through techniques.

Overview and History

Definition

The default mode network (DMN) is a large-scale network characterized by increased activity during wakeful rest, , and internally directed , in contrast to task-positive networks that engage during externally focused, goal-directed activities. This network supports mental processes oriented toward the self and personal experiences rather than immediate environmental demands. Key characteristics of the DMN include heightened activation during , self-referential processing, and retrieval, which facilitate reflection on one's past, present, and future. It typically deactivates during cognitively demanding external tasks, such as attention-requiring perceptual or motor activities, underscoring its role in toggling between internal and external modes of brain function. The DMN was initially identified through () studies that observed consistent deactivations across multiple tasks, revealing a baseline state of organized activity negatively correlated with performance on goal-directed behaviors. The term "default mode network" was coined by Marcus E. Raichle and colleagues in 2001 to denote this intrinsic system active in the absence of deliberate, externally oriented actions. Core regions of the network include the , medial , and .

Discovery and Evolution

The concept of the default mode network (DMN) emerged from early observations in the , when (PET) and (fMRI) studies revealed consistent deactivations in specific brain regions during goal-directed tasks, indicating "task-unrelated" or baseline activity. These findings, initially noted as unexpected negative signals in attention-demanding paradigms, suggested an organized pattern of brain function active during rest or , contrasting with task-induced activations. A pivotal milestone occurred in 2001, when Raichle and colleagues formalized the "default mode" term in a seminal PNAS paper, linking these deactivations to a metabolic baseline state suspended during focused behaviors, based on meta-analyses of data showing coordinated decreases in midline and parietal cortices. This work shifted the paradigm from viewing rest as mere idleness to recognizing it as an active, energy-consuming integral to function. Through the , the concept evolved with the integration of resting-state fMRI, as demonstrated by Greicius et al. in 2003, who applied network analysis to show intrinsic functional connectivity within the DMN during task-free conditions, providing robust evidence for its coherence as a synchronized system. Further refinement came in 2010, when Andrews-Hanna et al. delineated DMN subsystems through functional-anatomic fractionation, identifying distinct core, dorsal medial prefrontal, and medial temporal components with specialized connectivity patterns using task-based and resting-state fMRI. The 2010s marked a broader shift toward functional parcellation studies, employing large-scale meta-analyses and advanced imaging to subdivide the DMN into finer modules supporting varied cognitive domains, enhancing precision in mapping its internal organization. By 2025, this evolution incorporated postmortem histology, as in a Nature Neuroscience study by Paquola et al., which combined cytoarchitectonic data with in vivo neuroimaging to reveal laminar-specific architecture and signal flow within DMN regions, offering histological validation of its microstructural foundations.

Neuroanatomy

Core Regions

The default mode network (DMN) comprises a set of bilateral and symmetrical cortical regions primarily located in the medial prefrontal, posterior cingulate/precuneus, inferior parietal, and temporal areas, which exhibit coordinated activity during periods of wakeful rest. These core regions form the foundational anatomical substrate of the DMN, with meta-analyses confirming their consistent involvement across studies, including the posterior cingulate cortex/precuneus (PCC/P) as the largest node by volume. Recent 2025 histological analyses using postmortem tissue have delineated the cytoarchitectonic boundaries of these regions, revealing heterogeneous layering patterns—such as denser granular layers in the PCC/P and more agranular features in the medial prefrontal cortex (mPFC)—that distinguish DMN nodes from adjacent unimodal sensory areas. The posterior cingulate cortex/precuneus (PCC/P) occupies the medial posterior , extending from the posterior aspect of the cingulate superiorly to the along the midline, bilaterally symmetric with peak coordinates around (0, -50, 30) in standard stereotactic space. As the central hub of the DMN, it integrates internal and external informational streams through its extensive cytoarchitectural gradients, featuring a broad expanse of Brodmann areas 23, 31, and 7 that support network-wide coordination. Histological examinations highlight its transitional boundaries with the , marked by shifts in density and myelination. The medial prefrontal cortex (mPFC) is situated along the ventral and rostral medial , bilaterally encompassing subregions like the ventral mPFC (/11) and anterior cingulate, with key foci at approximately (±10, 50, -5). This region contributes to the DMN through its role in self-referential and processing, anatomically defined by its proximity to the orbital frontal cortex and characterized by thinner cortical layers compared to lateral prefrontal areas. Cytoarchitectonic studies confirm its boundaries via distinct laminar organization, including a prominent layer III for associative processing. The inferior parietal lobule (IPL), including the , lies in the lateral parietal cortex, bilaterally symmetric with the left centered at (-45, -70, 30) and its right homolog at (45, -70, 30), forming part of Brodmann areas 39 and 40. It supports and spatial navigation within the DMN, with anatomical features such as folded gyral patterns that enhance surface area for integration. Recent histological mapping reveals precise boundaries with the , delineated by variations in distribution. Temporal regions of the DMN include the middle and hippocampal formation, located ventrally in the ; the middle spans bilaterally around (±50, -40, -10) in 21, while the hippocampal formation resides medially within the medial , extending from the to the splenium. These areas facilitate integration, with the middle providing associative links via its sulcal architecture and the contributing through its curved, trilaminar structure. The 2025 cytoarchitectonic analyses underscore their heterogeneous boundaries, with the hippocampal subfields showing distinct somatic layering that interfaces with parahippocampal regions.

Connectivity and Subnetworks

The default mode network (DMN) exhibits intrinsic functional connectivity characterized by synchronized low-frequency fluctuations (<0.1 Hz) in the blood-oxygen-level-dependent (BOLD) signal during rest, as observed in functional magnetic resonance imaging (fMRI) studies. This connectivity pattern reflects coordinated activity among core DMN regions, such as the posterior cingulate cortex (PCC) and medial prefrontal cortex (mPFC), without external task demands. Structurally, the DMN is supported by tracts, including the cingulum bundle, which links the to the mPFC and extends connections to the , facilitating information transfer across these hubs. Diffusion tensor imaging has revealed that the integrity of these tracts, measured by , correlates with the strength of functional connectivity between the mPFC and . The DMN can be parcellated into distinct subnetworks based on functional connectivity profiles: the core subsystem, involved in self-referential and conceptual processing; the dorsal medial subsystem, involved in and mentalizing; and the medial temporal subsystem, associated with and future simulation. This tripartite organization, identified through seed-based connectivity analyses, highlights how these subsystems interact to support internally directed cognition. A key feature of DMN organization is its anti-correlation with the salience network, where task-evoked activation in the salience network suppresses DMN activity, enabling shifts between internal and external focus. Graph theory analyses further describe the DMN as a highly integrated module, with elevated modularity scores indicating strong within-network cohesion relative to other large-scale brain networks. Recent biophysical modeling efforts in 2025 have quantified synaptic coupling strengths between DMN hubs, revealing that excitatory-inhibitory balance modulates network dynamics and vulnerability to dysfunction in disorders like . These models integrate structural with neural simulations to predict how variations in coupling influence overall DMN integrity.

Functions

Cognitive Roles

The default mode network (DMN) supports a range of internally directed cognitive processes that facilitate reflection, simulation, and integration of personal and social experiences. These functions emerge prominently during periods of low external demand, enabling the brain to generate and manipulate mental representations without ongoing sensory input. Key roles include self-referential thinking, retrieval, prospection, and , which collectively contribute to a coherent sense of and adaptive . Self-referential thinking, involving the evaluation of personal traits and , is a core function of the DMN, particularly through its medial subsystem. This process allows individuals to form judgments about their own characteristics, such as personality attributes, and supports the construction of an ongoing narrative of the . For instance, studies demonstrate heightened DMN activity during tasks requiring trait attribution to oneself compared to others. , an extension of self-referential processing, engages the DMN to infer others' mental states by drawing analogies from one's own experiences, aiding in and social understanding. Autobiographical memory retrieval relies heavily on the DMN's posterior cingulate and medial components, which integrate episodic details to reconstruct past events. This network facilitates the vivid reliving of personal experiences, enabling emotional and contextual richness in recall. The DMN also underpins episodic future thinking by simulating potential future scenarios, often by recombining elements from past memories to envision hypothetical outcomes. Such prospection supports and by projecting self-relevant narratives forward in time. Mind-wandering, characterized by spontaneous shifts to internal thoughts, is closely tied to DMN activity and often involves daydreaming about personal goals or unresolved issues. This state links to , as unconstrained ideation within the DMN fosters novel associations and insights. Research indicates that DMN-mediated enhances adaptive behaviors by allowing rehearsal of future events in a manner from the present . In , the DMN contributes to understanding others' perspectives via its medial prefrontal regions, which process attributions during . Recent studies highlight the DMN's role in constructing situation models—integrated mental representations of ongoing events and characters' intentions—essential for following stories or social interactions. For example, 2025 functional connectivity analyses show sustained DMN-semantic network coupling during processing to maintain these models over time. The DMN deactivates during focused, goal-directed tasks to prioritize external .

Underlying Mechanisms

The default mode network (DMN) exhibits prominent oscillatory dynamics during resting states, particularly in its posterior regions such as the and , where alpha (8–12 Hz) and (13–30 Hz) rhythms predominate. These oscillations facilitate intrinsic communication within the network, with alpha rhythms showing enhanced that modulates local activity and supports the network's baseline functioning. Beta oscillations contribute to patterns, enabling flexible interactions among core DMN hubs even in the absence of external stimuli. Such electrophysiological patterns underscore the DMN's role in sustaining internal mentation through rhythmic neural . Biophysical models of DMN activity emphasize Hebbian mechanisms to maintain its intrinsic connectivity, where correlated neural firing strengthens synaptic weights according to "cells that fire together wire together." This process refines resting-state functional connectivity by reinforcing recurrent loops within the network, particularly in the medial prefrontal cortex (mPFC). Computational models demonstrate how excitatory feedback circuits amplify and stabilize DMN signals, contributing to its persistent activity during . These models integrate biophysical parameters like synaptic efficacy and neuronal excitability to predict network resilience against disruptions. The DMN integrates with other large-scale networks through dynamic switching mediated by the frontoparietal control network, which toggles between internal and external focus. This interaction often manifests as anticorrelations, where DMN activity decreases as task-positive networks activate. In functional MRI (fMRI) studies, these anticorrelations are quantified using Pearson coefficients between of DMN and frontoparietal regions, typically yielding negative values (e.g., ρ ≈ -0.2 to -0.5) that reflect competitive . Functional connectivity between DMN regions i and j is commonly defined as: \rho_{ij} = \corr(\text{BOLD}_i(t), \text{BOLD}_j(t)) where \text{BOLD}_i(t) and \text{BOLD}_j(t) are the blood-oxygen-level-dependent signals over time t, providing a metric for intrinsic coupling. Despite its designation as a "resting" network, the DMN imposes substantial metabolic demands, with glucose utilization in core regions like the posterior cingulate showing one of the highest levels of metabolic activity in the brain during rest, supporting ongoing spontaneous activity, highlighting the network's energy-intensive nature even without overt cognitive demands. In 2025 reviews, the DMN is positioned as a core hub for consciousness, facilitating self-referential awareness and the integration of internal states within broader self-awareness networks.

Development and Modulation

Lifespan Development

The default mode network (DMN) begins to emerge prenatally, with rudimentary functional connectivity detectable in the third trimester of gestation through fetal (fMRI). Studies using integrated 4D fMRI reconstruction have identified nascent DMN components, including connections between the (PCC) and medial prefrontal cortex (mPFC), as early as 29-43 weeks , indicating the onset of intrinsic network organization before birth. In early infancy, this connectivity strengthens rapidly within the first postnatal month, reflecting the transition from fetal to neonatal brain maturation. During childhood and , the DMN undergoes significant maturation, particularly in the strengthening of PCC-mPFC links around ages 9-12, which aligns with the of self-concept and social-cognitive abilities. Functional connectivity within the DMN increases progressively from childhood to young adulthood, with enhanced integration of core hubs supporting internal mentation and self-referential processing. This period marks a shift toward more efficient , as evidenced by longitudinal studies showing protracted of DMN subsystems. In adulthood, DMN integration reaches its peak in mid-life, around age 50, characterized by optimal functional connectivity strength and anticorrelations with task-positive networks. Following this, a gradual decline occurs post-60, with reduced long-range connectivity and weakened anticorrelations, contributing to subtle shifts in . These age-related changes are observed consistently in resting-state fMRI across large cohorts. In aging, alterations in DMN connectivity can signal precursors to , including hyperconnectivity in posterior regions like the PCC in early stages, preceding widespread hypoconnectivity. Such hyperconnectivity may reflect compensatory mechanisms before pathological decline. The development of the DMN is influenced by both genetic and environmental factors, with heritability estimates for functional connectivity ranging around 40-50% based on twin studies. Genetic contributions shape baseline , while environmental influences, such as early social exposure, modulate connectivity strength and resilience during critical developmental windows.

External Influences and Interventions

External influences on the default mode network (DMN) encompass a range of pharmacological, non-invasive, , and technological interventions that modulate its activity and . These approaches have been investigated for their potential to alter DMN , often targeting core regions like the (PCC) or medial prefrontal cortex to influence processes such as and self-referential thinking. Pharmacological agents, particularly psychedelics and antidepressants, exert notable effects on DMN dynamics. administration desynchronizes the DMN by decreasing functional within its core hubs and increasing overall brain entropy, leading to more fluid and less rigid network states that persist for weeks post-dose. This entropy increase is thought to underlie the compound's capacity to disrupt habitual thought patterns. In contrast, antidepressants, such as the serotonin-norepinephrine (SNRI) , reduce DMN hyperconnectivity in individuals with , normalizing it to levels observed in healthy controls after several weeks of treatment. Non-invasive techniques offer targeted modulation without systemic effects. (TMS) applied to the disrupts DMN activity, thereby reducing and associated behavioral variability in experimental settings. Similarly, mindfulness meditation practices enhance anticorrelations between the DMN and task-positive networks, such as the central executive network, promoting greater network flexibility and reduced self-referential rumination after consistent training. Lifestyle factors also influence DMN integrity. Acute fragments within-network connectivity in the DMN, diminishing its anti-correlations with networks and impairing rest-task switching. Conversely, regular strengthens connectivity between the and DMN regions, with higher levels predicting enhanced functional coupling that supports and cognitive . Specific interventions like real-time functional magnetic resonance imaging (rt-fMRI) have shown efficacy in modulating DMN activity during the 2020s. Protocols targeting DMN downregulation, often combined with , reduce its functional connectivity in clinical populations, with trials demonstrating sustained symptom improvements in and . Technological advances in animal models provide causal insights into DMN modulation. Optogenetic stimulation of anterior neurons in rats suppresses DMN activity by inhibiting engagement, confirming the salience network's regulatory role over DMN states during salient stimuli processing. Similarly, activating parvalbumin neurons optogenetically induces DMN-like behaviors without affecting memory encoding, highlighting subcortical contributions to network orchestration.

Clinical Aspects

Associations with Disorders

The default mode network (DMN) exhibits alterations across various psychiatric and neurological disorders, often manifesting as disrupted connectivity patterns that correlate with symptom severity and cognitive impairments. These changes, identified through resting-state (fMRI), highlight the DMN's role in self-referential processing and its vulnerability in , contrasting with its typical anticorrelations with task-positive networks in healthy individuals. In mood disorders, (MDD) is characterized by hyperconnectivity within the DMN, particularly involving the medial prefrontal cortex (mPFC), which is linked to increased rumination and negative self-focused thought. A of resting-state fMRI studies confirmed hyperconnectivity between DMN seeds and the mPFC in MDD patients compared to controls. Similarly, elevated functional connectivity between the DMN and subgenual prefrontal cortex (a subregion of the mPFC) has been observed in individuals with depressive rumination. In contrast, shows hypoactivation in DMN regions, such as the (PCC), even during euthymic states, potentially contributing to mood instability. Persistent DMN hypoactivation has been reported in bipolar patients with a history of , suggesting a trait-like marker of the condition. Neurodegenerative conditions like (AD) feature prominent DMN pathology, including in the , a core DMN hub, which appears in early disease stages and correlates with memory decline. This disrupts posterior cingulate networks, leading to hypometabolism and reduced DMN integrity. DMN fragmentation, evidenced by decreased connectivity in the PCC and , serves as an early for preclinical AD, preceding overt cognitive symptoms. Schizophrenia is associated with reduced anticorrelations between the DMN and task-positive networks, such as the , which may underlie reality distortion and impaired reality monitoring. This decoupling contributes to excessive DMN intrusion during goal-directed tasks, exacerbating positive symptoms like hallucinations. In neurodevelopmental disorders, youth with attention-deficit/hyperactivity disorder (ADHD) display immature DMN connectivity patterns, including atypical functional connections that lag behind typical developmental trajectories. A revealed delayed maturation of DMN architecture in adolescents with ADHD, linked to heightened interference from the DMN during attention-demanding tasks. Similarly, in children and adolescents shows disrupted DMN development, with patterns of both over- and underconnectivity that persist from childhood into adolescence, associating with deficits. Recent underscores the DMN's transdiagnostic , with a 2025 study in non-clinical populations linking reduced DMN functional connectivity to subtle cognitive deficits, such as impaired executive function. Furthermore, DMN connectivity alterations emerge as a transdiagnostic for cognitive dysfunction across disorders, predicting impairment severity independently of specific diagnoses.

Diagnostic and Therapeutic Applications

The default mode network (DMN) has emerged as a key biomarker in clinical diagnostics, particularly through resting-state functional magnetic resonance imaging (rs-fMRI), which measures connectivity changes to predict disease progression. In Alzheimer's disease, decreased DMN connectivity, especially within the posterior cingulate cortex and medial prefrontal cortex, serves as an early indicator of progression from mild cognitive impairment to dementia, with longitudinal studies showing that such declines predict conversion to Alzheimer's with high accuracy over 2-3 years. For instance, effective connectivity models of the DMN have demonstrated single-participant level prediction of future dementia diagnosis up to several years in advance. In predictive imaging for psychiatric conditions, models leveraging DMN patterns have shown promise in forecasting relapse risk. Specifically, in , classifiers trained on resting-state functional connectivity (RSFC) within the DMN can predict relapse on an individual basis, with alterations in core DMN subsystems explaining significant portions of symptom variability. Reduction in DMN RSFC during treatment phases has been linked to sustained remission over two years, highlighting its utility in risk stratification. Therapeutically, interventions targeting the DMN aim to normalize its hyperactivity or dysconnectivity associated with maladaptive processes. (CBT), particularly rumination-focused variants, reduces self-referential rumination by attenuating DMN connectivity, leading to decreased activity in regions like the subgenual and improved emotional regulation. In , (DBS) of the subthalamic nucleus modulates DMN functional connectivity, potentially alleviating apathy by restoring network balance and correlating with psychiatric symptom improvements. Recent 2025 evidence supports DMN-guided precision medicine in , where neuroimaging-informed approaches like (TMS) target individualized DMN connectivity to enhance treatment response in and related disorders. However, challenges in standardization, such as variability in DMN parcellation across scanners and populations, limit widespread adoption. Meta-analyses indicate that DMN metrics account for 20-30% of variance in symptom prediction across disorders like and Alzheimer's, underscoring their moderate but clinically meaningful prognostic value while emphasizing the need for .

Debates

Criticisms

One major methodological criticism of default mode network (DMN) research centers on the variability introduced by (fMRI) preprocessing pipelines, which can lead to inconsistent definitions of DMN nodes and reduced detectability of the network. Different pipelines, including variations in motion correction, spatial normalization, and global signal , have been shown to substantially alter the and strength of DMN , particularly in clinical populations where signal is compromised. Additionally, head motion artifacts during resting-state fMRI scans inflate short-distance functional while diminishing long-distance connections within the DMN, creating spurious patterns that mimic true network activity even after standard corrections. These issues highlight how technical choices in can undermine the reliability of DMN findings across studies. Conceptually, the DMN framework has been critiqued for overemphasizing "resting-state" conditions, which may lack by isolating the brain from naturalistic, task-embedded contexts where internal mentation occurs. This focus on quiet ignores how DMN activity persists or modulates during passive or everyday behaviors, potentially misrepresenting its role in real-world . Furthermore, debates persist on whether the DMN truly represents a "default" mode or is instead highly context-dependent, with evidence showing task-related activations that challenge the rest-task originally proposed. Such critiques argue that the label "default" oversimplifies the network's flexible integration with other systems during adaptive thought processes. Reproducibility concerns have plagued DMN research, particularly in the , with failed replications of subnetwork functions in large-scale cohorts revealing inconsistencies in identifying core nodes like the medial subdivisions. For instance, efforts to delineate , ventral, and anterior medial subregions within the DMN have yielded variable results across datasets, underscoring lingering issues in functional parcellation. These failures are exacerbated by small sample sizes and insufficient statistical in early studies, contributing to broader replication crises in that question the robustness of DMN connectivity metrics. A 2023 review synthesizes evidence for the DMN's causal roles in and disorders, drawing from correlational and interventional data, while noting the need for advanced methods to clarify directionality and mechanisms. Critics note that assumptions of causality in DMN dysfunction for disorders often stem from observational fMRI, overlooking variables like individual variability in . Animal model limitations further compound these issues, as and nonhuman DMNs exhibit organizational gaps compared to humans, particularly under , which potentially alters network dynamics and limits translation to human processes. These translational challenges limit the generalizability of preclinical findings to human .

Nomenclature and Conceptual Shifts

The term "default mode network" (DMN) was first introduced by Marcus Raichle and colleagues in 2001 to describe a set of regions exhibiting consistent decreases in activity during goal-directed tasks, reflecting a baseline state of brain function akin to metabolic defaults observed in studies. This nomenclature emphasized the network's prominence during rest, contrasting it with task-positive networks, and arose from the need to explain unexpected deactivations in data. Alternative terms have emerged to highlight different aspects of the network's role, such as "intrinsic network," which underscores its endogenous activity independent of external stimuli, and "mind-wandering network," capturing its association with spontaneous, self-referential thought. These labels reflect evolving emphases on the DMN's internal dynamics rather than mere opposition to task engagement. Conceptual shifts have moved from viewing the DMN as a static resting-state system to a dynamic entity that fluctuates with cognitive and emotional states, integrating across networks. Recent 2025 models of consciousness position the DMN as an integrative core, serving as a nexus for convergence and divergence of neural signals to support unified awareness. This dynamic perspective aligns with evidence of time-varying connectivity patterns linked to varying states. Debates persist regarding the inclusivity of DMN subsystems, particularly the distinction between ventral and dorsal components, where the ventral medial subsystem (involving medial temporal regions) supports vivid, episodic simulation, while the dorsal medial subsystem (including ) aids in conceptual and social inference, raising questions about unified versus modular definitions. Integration with (GWT) is another focal point, with recent syntheses proposing the DMN as a synergistic "gateway" that broadcasts internally generated content for conscious access, bridging GWT's ignition mechanisms with the network's role in self-referential processing. In publications, the DMN has been reframed as a "narrative network" facilitating the construction and maintenance of situation models during story comprehension, where its connectivity with semantic systems enables ongoing integration of contextual elements into coherent mental representations. Critiques highlight an anthropocentric bias in DMN research, as comparative studies reveal organizational gaps—such as weaker medial connectivity in non-human like —challenging assumptions of full and urging broader cross-species validation to avoid human-centric overgeneralizations.