Skip to main content

PERSPECTIVE article

Front. Psychol., 11 November 2020
Sec. Environmental Psychology
This article is part of the Research Topic The Benefits of Nature-Based Solutions to Psychological Health View all 8 articles

The Self and Its Nature: A Psychopathological Perspective on the Risk-Reducing Effects of Environmental Green Space for Psychosis

  • Department of Neuroscience, Imaging and Clinical Sciences, Institute of Advanced Biomedical Technologies (ITAB), G. d’Annunzio University of Chieti-Pescara, Chieti, Italy

Epidemiological studies have shown that environmental green space contributes to the reduction of psychosis incidence in the population. Clarifying the psychological and neuro-functional mechanisms underlying the risk-decreasing effects of green surroundings could help optimize preventive environmental interventions. This perspective article specifically aims to open a new window on the link between environmental green space and psychosis by considering its core psychopathological features. Psychotic disorders, such as schizophrenia, are essentially characterized by self-disturbances. The psychological structure of the self has been described as a multidimensional phenomenon that emerges from the reciprocal interaction with the environment through intrinsic and extrinsic self-processes. The intrinsic self refers to the experience of mental activity and environmental information as inherently related to one’s own person, which involves self-referential processing, self-reflection, memory, interoception, and emotional evaluation. The extrinsic self refers to sensorimotor interactions with the environment and the sense of agency, that is, the experience of being the source of one’s own actions and the multisensory consequences thereof. In psychosis, anomalous self-processing has been related to a functional fragmentation of intrinsic and extrinsic self-processes and related brain networks. Moreover, evidence from cognitive neuroscience suggests that green space could have beneficial effects on self-related processing. Based on the literature, it could be hypothesized that self-processing is involved in mediating the beneficial effects of green space for psychosis. Considering the multidimensionality of the self, it is proposed that urban green space design aimed at improving mental health ideally impacts the complexity of self-facets and thus restores the individual’s self.

Introduction

Psychotic disorders are severe mental illnesses that involve a “loss of vital contact with reality” (Minkowski, 1927; Parnas and Henriksen, 2014). The most studied and pervasive psychotic disorder is likely schizophrenia, but psychotic episodes can happen in various psychiatric, neurological, and neurodevelopmental conditions and can also be induced by the use of medications or psychoactive drugs. Socioeconomically, psychosis has been associated with premature mortality, morbidity, financial and social burdens, and poor outcomes (Rössler et al., 2005; van Os and Linscott, 2012; Fazel et al., 2014). Psychoses, particularly schizophrenia, place large demands on public healthcare and its budgets (Rössler et al., 2005).

The high heritability of psychosis indicates the existence of genetic risk factors (Smigielski et al., 2020), although genetic components cannot fully explain the development of psychosis (van Os et al., 2010; Pries et al., 2018; Torrey and Yolken, 2019). The risk of developing a psychosis during one’s life is also determined by biological, psychological, and social factors (McGrath et al., 2004; van Os et al., 2010; Fusar-Poli et al., 2017). This knowledge provides important information for intervention programs aimed at detecting high-risk individuals and preventing them from becoming psychotic (Ruhrmann et al., 2010; van Os et al., 2017). However, the implementation of large-scale intervention strategies is still limited. In addition to therapeutic interventions (McGorry et al., 2009; Fusar-Poli et al., 2019), other possibilities for preventive intervention have been implied. Epidemiological studies suggest that environmental factors are involved in the development of psychosis as well (van Os et al., 2010; Dragt et al., 2011; Fusar-Poli et al., 2017). Moreover, longitudinal studies suggest that the modulation of psychosis incidence through environmental factors likely involves causal relationships that cannot be explained by other mediating epidemiological variables (van Os et al., 2010).

Some of these factors may be attractive targets for global risk-reducing environmental interventions (Sussman and Hollander, 2014). Among the various environmental factors that have been related to psychosis risk, urbanicity has been consistently associated with an elevated risk of psychosis as compared to living in rural environments (Lewis et al., 1992; Pedersen and Mortensen, 2001; Sundquist et al., 2004; van Os et al., 2004; Newbury et al., 2016; see for reviews, Krabbendam and van Os, 2005; Kelly et al., 2010). Given that the majority of the world population currently lives in urban areas and continues to increase, this is an issue of concern for mental healthcare (United Nations, Department of Economic and Social Affairs, Population Division, 2014). One notable difference between urban and rural environments that has recently received increasing attention in the scientific literature concerning environmental effects on mental health is the quantity and kind of natural or green space (Verheij et al., 2008), which could be hypothesized as constituting a risk-modulating factor for psychosis. In the present article, I will specifically examine the utilization potential of green space to reduce the incidence of psychosis, although it should be emphasized that the diminished availability of green space is by no means the only characteristic of urban environments and that psychosis incidence in the population is likely modulated by a complexity of interacting nvironmental and genetic factors (Tsuang, 2000; Schmitt et al., 2014).

In particular, this perspective article aims at developing a new hypothesis regarding the psychological and neuronal mechanisms that could explain the risk-decreasing effects of natural surroundings for psychosis. For the purpose of focus, an investigation of how the effects of green space on psychosis incidence can be embedded in the full complexity of genetic and environmental factors and events remains beyond the scope of the present article, although, this will be a mandatory topic for ensuing dialog. A better understanding of the underlying risk-reducing mechanisms of concrete environmental features could help in optimally exploiting these features in urban design. Given the fact that structural and direct investigations in compromising mental disorders like psychosis are still sparse, one approach to exploring these mechanisms would be to link the core psychopathological features of psychosis to green space effects.

Green Space Exposure is Related to Reduced Psychosis Risk

Natural environments usually refer to surroundings that include green space (essentially typified by the presence of vegetation) but also can include blue space (water bodies), which could be developed with or without human intervention (Völker and Kistemann, 2011; Bratman et al., 2012; Smith et al., 2017). The definition of green space, as used in studies that investigate its psychological effects through experience, covers a broad range of environments, from pristine nature to human cultivated gardens, and more specifically includes urban greens, forests/woodlands, countryside/farmland, and the wilderness (Bratman et al., 2012). Urban green space, in turn, can be characterized by the more formal or informal design of gardens and parks (Twedt et al., 2016). The efficiency of green space exposure in modulating health and well-being has been studied more generally in terms of the presence of green space in people’s living environments and also more specifically in terms of visual exposure (e.g., window views and virtual environments) and physically spending time in or interacting with green space (Bratman et al., 2012).

The beneficial effects of natural surroundings on daily life have been shown for physical and mental health, social well-being, academic and job performance, and happiness (Hartig, 1993; Maas et al., 2009; Bratman et al., 2012; White et al., 2013; Hartig et al., 2014; Cohen-Cline et al., 2015; James et al., 2015; van den Berg et al., 2015; Sarkar et al., 2018). Although the nature of such effects remains to be clarified, natural surroundings, as compared to urban areas, are generally thought to decrease air and noise pollution, improve social cohesion and stress regulation, facilitate the restoration of attention and fatigue, improve the mood, and reduce depressive symptoms (Kaplan and Kaplan, 1989; Ulrich et al., 1991; Berman et al., 2008; Bratman et al., 2012; Markevych et al., 2017; Twohig-Bennett and Jones, 2018). A recent study highlighted the relevance of environmental interventions by showing that individuals frequenting urban environments with few green resources and an increased risk for mental illness are particularly receptive of the presence of urban green space (Tost et al., 2019). Some further evidence suggests that being exposed to real green and blue space induces psychophysiological and behavioral responses that can be differentiated from those induced by the same environments when reproduced by visual media (Huang, 2009; Huang et al., 2019). Similarly, a recent meta-analysis showed that real natural settings benefit mood to a greater degree than simulated settings (Browning et al., 2020).

To date, the relationship between the presence of residential natural spaces and a lower risk for psychosis has been investigated by few studies. Boers et al. (2018) showed that psychotic patients had a significantly lower amounts of available green space (agricultural areas, natural areas, and artificially installed greenery) but not blue space near their residence, while controlling for age, gender, urbanicity, and socioeconomic status. The same study did not find any significant relationship between green space and the length of stay in a psychiatric ward as a measure of illness severity. However, because no other measures of illness severity were included, further studies may need to consider more direct measures as well, including illness impact and symptomatology. A nation-wide, population-based study including more than 900,000 people showed that a decreased presence of green space near one’s residence during childhood (calculated as the normalized difference vegetation index, NDVI, based on remote sensing satellite images) was associated with higher incidence rate ratios for many psychiatric disorders, including schizophrenia and related psychotic disorders (Engemann et al., 2019a). A dose-response relationship over time was also observed in this study, and the lowest levels of green space were associated with up to a 55% higher risk of psychiatric disorders. Additionally, when adjusting for urbanization, parents’ socioeconomic status, family history, parental age, and municipal socioeconomic factors, these effects remained significant for most disorders. Another nation-wide population-based study by the same group focusing on schizophrenia further showed a dose-response relationship between the amount of residential green space present during childhood (NDVI), but not green space heterogeneity, and the risk of developing schizophrenia later in life (Engemann et al., 2018). Also, in this case, the results remained stable after adjustment for urbanization, age, sex, and socioeconomic status. Finally, in a series of follow-up studies, Engemann et al. (2019b) more specifically associated agricultural areas and near-natural green and blue space with lower schizophrenia rates as compared to urban areas, whereas vegetation density (NVDI) was negatively associated with schizophrenia rates in a dose-response manner independently for urban and agricultural areas. Moreover, based on hazard ratios, additive effects on schizophrenia risk were found for childhood green space exposure (NVDI close to residence based on remote sensing satellite images) and genetic liability, while an interaction between these factors could not be detected (Engemann et al., 2020). Taken together, these epidemiological results suggest that the presence of and access to natural surroundings in rural and urban areas may reflect a modulatory environmental factor that contributes to the prevention of psychosis and that green space effects may be disentangled from urbanicity and genetic effects.

Disrupted Self-Processing is a Core Feature of Psychosis

One of the questions that is derived from these studies is “What are the critical aspects of psychosis that might be influenced by green space?” From a historical, psychopathological perspective, schizophrenia and related psychotic disorders have been described as self-disorders (Raballo et al., 2011). Building on these early insights, more recently, psychosis has been characterized as a complexity of self-disturbances that is generally described by an exaggerated self-consciousness and a disrupted sense of owning one’s personal perceptions and thoughts (Sass and Parnas, 2003; Nelson et al., 2014). Because self-disturbances are often reported as subclinical phenomena that have already occurred prior to the onset of psychosis, remain stable after the attenuation of frank psychotic symptoms, and are highly predictive of conversion to psychosis, self-disturbances are commonly considered to reflect the core features of psychosis (Schultze-Lutter, 2009; Nelson et al., 2012). These properties of self-disturbances make them interesting targets for preventive intervention programs. Indeed, as reviewed above, green space may positively act on the mechanisms underlying psychosis onset during childhood.

To develop a more concrete understanding of the exact nature of self-disturbances in psychosis, it is useful to take a closer look at the psychological structure of the self-concept. The self and its disturbance have been increasingly portrayed from multiple perspectives in psychology and cognitive neuroscience. A major distinction is that between intrinsic and extrinsic self-processes (Gallagher, 2000; Vanhaudenhuyse et al., 2011), which can be traced to the self-aspects of the “Me,” as the conscious person who is known by himself or herself (e.g., “this is me”), and the “I,” who experiences and interacts with the environment (e.g., “I did that”), as described by James (1890). Specifically, intrinsic self-processing refers to the perception of information as belonging to oneself or as personally relevant, which allows self-reflection and experiencing a sense of identity (Damasio, 1999; Northoff and Bermpohl, 2004; van der Meer et al., 2010). This is mainly an internally directed process that integrates stimuli and thoughts with inner information from memory, personal narrative, and interoception and is related to emotional evaluation through the link with transient bodily states (Northoff and Panksepp, 2008; van der Meer et al., 2010; Qin and Northoff, 2011). In contrast, extrinsic self-processing regards the experience of oneself as the source of one’s own actions and their consequences, that is, the perception of oneself as an entity with a sense of agency (Gallagher, 2000; Haggard, 2017). It can be conceived of as an externally directed process based on the experience of one’s intentional control over the environment through action (Jeannerod, 2003; Gallese and Sinigaglia, 2010). Action-related processes that could be involved include multisensory integration, self-monitoring, and sensorimotor predictions (Blanke, 2012). For instance, the integration of predicted somatosensory, motor, visual, and proprioceptive perceptions with the actual multisensory action consequences is crucial for a coherent self-experience during intentional behavior (Frith et al., 2000; van Kemenade et al., 2019).

This literature suggests that the self is composed of distinguishable but complementary processes. Such processes have been associated with largely distinct brain networks (Vanhaudenhuyse et al., 2011). However, in order to permit self-awareness, the networks involved in intrinsic and extrinsic self-processing (e.g., default mode, sensorimotor, attention, and executive networks) likely interact (Molnar-Szakacs and Uddin, 2013), possibly with an additional modulatory role for the salience network in the insula (Menon and Uddin, 2010). Indeed, recent empirical findings from neuroimaging (Di Plinio et al., 2020) suggest that intrinsic and extrinsic self-processes constitute a multidimensional phenomenon that emerges from a bidirectional interaction between an internal self and its external environment, where such interactions could be facilitated by efficient information exchange and integration across intrinsic and extrinsic self-networks in the brain.

Considering psychosis from this perspective, it can be proposed that anomalous intrinsic and extrinsic self-processes, as well as their functional imbalance, could explain self-disturbances. In particular, it has been proposed that the experience of a disrupted sense of self in its reciprocal interaction with the environment in psychosis could be explained by the fragmented functioning of intrinsic and extrinsic self-networks (Ebisch and Aleman, 2016). Furthermore, a biopsychological neural model has been proposed to describe how psychotic symptoms can be explained via a disequilibrium of network states and interference between network activities due to impaired auto-excitation and collateral inhibition (Looijestijn et al., 2015). As a consequence, at the phenomenological level, the distinction between internally and externally generated information may blur, leading to impaired self-recognition, depersonalization, and the tendency to experience one’s thoughts, internal speech, or actions as belonging to an external agent or force, rather than oneself (Kircher and Leube, 2003; Nelson et al., 2009; Waters et al., 2012). Because whether and how the beneficial effects of natural surroundings on psychosis can be related to these self-disturbances remain poorly understood, attempts to clarify this issue would require examining the way in which environmental factors associated with natural spaces affect the cognitive and neural mechanisms underlying self-related processing.

Can Green Space Improve Self-Processing?

To address this particular question in more detail, a literature search was performed for articles empirically investigating the relationship between green space and self-processing. PubMed and Google Scholar were screened for peer-reviewed articles published from January 1990 to June 2020, using the terms “self” AND “nature experience” OR “nature exposure” OR “green space” OR “natural space.” Similar searches were performed for studies considering self-disturbances, using the terms “psychosis” OR “schizophrenia” AND “self” AND “nature experience” OR “nature exposure” OR “green space” OR “natural space.” Articles that resulted from these searches and relevant references cited in those articles were reviewed, and this selection was further completed by searches in the author’s personal files, where articles published in English were included. The literature search results showed that this specific issue received limited attention. After close inspection of the articles’ content, seven empirical studies were found to be relevant to the present perspective article (i.e., Hunter et al., 2010; Lederbogen et al., 2011; Margalit and Ben-Ari, 2014; Bratman et al., 2015; Hayhurst et al., 2015; Fuller et al., 2017; O’Brien and Lomas, 2017), which are discussed below.

A recent systematic review (Mygind et al., 2019) concluded that there is conditional evidence in children and adolescents for a beneficial effect on the part of diversified nature experiences on self-efficacy, a concept closely related to the sense of agency, though this was based on studies with a note regarding the risk of biased results (mountain and lake activities in O’Brien and Lomas, 2017; wilderness therapy intervention in Margalit and Ben-Ari, 2014; outdoor residential experiences in countryside with woodland in Fuller et al., 2017; and developmental sail voyage experiences in Hayhurst et al., 2015, as well as in Hunter et al., 2010). Similarly positive effects were reported for self-esteem, resilience, and academic and cognitive performance, whereas evidence regarding self-concept, problem solving, and mood were inconclusive (see Mygind et al., 2019). In addition, some cognitive neuroscience studies began to provide relevant insights into the cognitive and neural mechanisms underlying the association between green space and self-processing. In a cross-sectional, functional magnetic resonance imaging (fMRI) study involving non-clinical, healthy individuals, Lederbogen et al. (2011) dissociated the impact of urban upbringing and city living on brain activity when participants were exposed to social evaluative stress. Their results showed that current city living was linked to increased amygdala activity, whereas urban upbringing affected the perigenual anterior cingulate cortex. In another fMRI study, Bratman et al. (2015) investigated the link between nature experiences (a 90-min walk in green space consisting of grassland with scattered trees, shrubs, and fauna, as well as views of hills and a bay, vs. an urban walk in a busy city thoroughfare) and rumination in a sample of non-clinical, healthy participants. Relevantly, rumination can be considered a dysfunctional self-process defined as a maladaptive pattern of self-referential thought and self-relational emotions. Behaviorally, the results showed that the nature experiences, as compared to the urban experiences, led to decreased rumination. Neuro-functionally, nature experiences, as compared to urban experiences, led to decreased neural activity (cerebral blood flow) in the subgenual prefrontal cortex and perigenual anterior cingulate cortex during rumination.

Notably, both fMRI studies (Lederbogen et al., 2011; Bratman et al., 2015) linked the ventromedial frontal cortex, specifically, the perigenual anterior cingulate cortex, to urbanicity or green experiences. Of interest, the perigenual anterior cingulate cortex has been identified as a crucial brain structure for many self-related processes that comprise self-continuity, self-consciousness, self-reflection, self-regulation, and self-other similarity (van der Meer et al., 2010; Northoff, 2017; Scalabrini et al., 2019). The perigenual anterior cingulate cortex is located in the default mode network, which is characterized by high levels of activity when individuals are involved in free thought, such as mind-wandering (Northoff et al., 2010). Moreover, the perigenual anterior cingulate cortex is a key node within a network that integrates information from the memory and interoception and is affected by its interactions with the anterior insula, medial temporal regions, and posterior cingulate cortex (Northoff and Panksepp, 2008). Regarding its involvement in psychosis, fMRI experiments applying explicit tasks of self-evaluation reported deficient intrinsic self-processing in the perigenual anterior cingulate cortex and adjacent ventromedial prefrontal cortices in patients with schizophrenia as compared to healthy controls (Modinos et al., 2011; Kühn and Gallinat, 2013; van der Meer et al., 2013; Tan et al., 2015).

Discussion

The evidence reviewed above begins to provide new insights into the mechanisms that may explain how green space exposure can reduce psychosis risk. On the one hand, epidemiological studies consistently show that green space exposure decreases the incidence of psychosis, whereas urbanicity is associated with an increased risk for psychosis. On the other hand, cognitive and neuroscience findings preliminarily suggest that exposure to and experiences of green space, as well as blue space, could have beneficial effects on self-related processing. Based on these findings, it is proposed that self-processing and related brain network interactions may constitute a relevant mechanism that mediates between green space exposure and psychosis risk (Figure 1).

FIGURE 1
www.frontiersin.org

Figure 1. A hypothetical model illustrating the modulation of the integrity of self-related processing, which is impaired in psychosis, through brain network interactions by green space. The experience of natural surroundings (green space area) in one’s living environment (A; increased interactions and overlap between green space and self-aspects) or being distantiated from natural surroundings during daily life (B; decreased interactions and overlap between green space and self-aspects) is associated with more or less integration of intrinsic (red; internally directed) and extrinsic (blue; externally directed) self-aspects, respectively. The green space photo depicts a view on Val d’Orcia in Tuscany, Italy, an UNESCO World Heritage landscape developed in the 14th and 15th centuries to idealize a well-balanced dialog between humans and nature.

Because this hypothesis has received very little or no attention in published empirical investigations using clinical samples and specific reports of positive and null results regarding the link between green space and psychosis-related self-disturbances are lacking, novel studies are encouraged to directly and systematically investigate how the environmental planning of green space could comprehensively facilitate intrinsic and extrinsic self-experiences in non-clinical samples, as well as in psychotic disorders or high-risk populations. The literature reviewed in this article provides concrete perspectives for further investigation. For example, psychological and neuroscientific studies with high levels of control over experimental conditions and modulating factors should reproduce the epidemiological findings. Moreover, definite issues for future studies of the health benefits of green space include the modulating effects of particular types and features of green space and the kind of interactions individuals have with green space on intrinsic/extrinsic self-processing and psychosis risk.

Further limitations of the present review must be mentioned. Because it focuses specifically on the risk-reducing effects of green space for psychosis, it is important to remember that the onset of psychosis depends on a multiplicity of factors and events. The lack of green space exposure is one out of many characteristics of urbanicity that contribute to psychosis risk, in addition to other physical, social, familiar, occupational, and relationship variables (van Os et al., 2010; Brown, 2011; Schmitt et al., 2014). Green space is a piece of an intricated puzzle of interactions between numerous environmental variables, as well as genetic factors, that explains the variance in psychosis onset. It will be crucial for future studies to increase our understanding of how the effects of green space can be embedded in this full complexity of factors, both to explain and prevent psychosis onset (Tsuang, 2000; Howes et al., 2004; Meyer-Lindenberg and Tost, 2012). Finally, in this article, the effect of green space on psychosis prevention is examined in the context of self-disturbances, which are the core features of psychosis and sensitive predictors of its onset, while the relationships with positive symptoms, social impairments, and reduced insight into illness are not considered. It would be relevant to expand this investigating by including these domains too.

In conclusion, self-awareness is a continuous, integrative phenomenon that emerges from a stream of sensory perceptions, actions, bodily states, memories, motivations, thoughts, and imaginations. These processes support a coherent sense of self with a past (autobiographical memories), a present (actual experiences), and a future (prospective thoughts). Green space may be an environment with auspicious qualities that can modulate mental and bodily self-experiences over time and space on various scales, transforming itself continuously as it evolves and changes over time, while at the same time remaining a familiar environment (Kuo, 2015; Northoff and Huang, 2017). It is therefore hypothesized that green space potentially reduces psychosis risk by offering a dynamic environment that within a complex architecture of environmental and genetic factors, supports a stable, multidimensional self-experience over time. Enhancing our knowledge about the exact relationships between green space experiences and multidimensional self-processing would help in environmental planning, especially in urban areas, to optimize the positive impact of green space on mental health and illness prevention.

Author Contributions

The author confirms being the sole contributor of this work, being responsible for reviewing the literature, developing the concept, and writing the manuscript, and has approved it for publication.

Funding

This work was supported by the “Departments of Excellence 2018–2022” initiative of the Italian Ministry of Education, University and Research for the Department of Neuroscience, Imaging and Clinical Sciences (DNISC) of the University of Chieti-Pescara.

Conflict of Interest

The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

Berman, M. G., Jonides, J., and Kaplan, S. (2008). The cognitive benefits of interacting with nature. Psychol. Sci. 19, 1207–1212. doi: 10.1111/j.1467-9280.2008.02225.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Blanke, O. (2012). Multisensory brain mechanisms of bodily self-consciousness. Nat. Rev. Neurosci. 13, 556–571. doi: 10.1038/nrn3292

PubMed Abstract | CrossRef Full Text | Google Scholar

Boers, S., Hagoort, K., Scheepers, F., and Helbich, M. (2018). Does residential green and blue space promote recovery in psychotic disorders? A cross-sectional study in the province of Utrecht, the Netherlands. Int. J. Environ. Res. Public Health 15:2195. doi: 10.3390/ijerph15102195

PubMed Abstract | CrossRef Full Text | Google Scholar

Bratman, G. N., Hamilton, J. P., and Daily, G. C. (2012). The impacts of nature experience on human cognitive function and mental health. Ann. N. Y. Acad. Sci. 1249, 118–136. doi: 10.1111/j.1749-6632.2011.06400.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Bratman, G. N., Hamilton, J. P., Hahn, K. S., Daily, G. C., and Gross, J. J. (2015). Nature experience reduces rumination and subgenual prefrontal cortex activation. Proc. Natl. Acad. Sci. U. S. A. 112, 8567–8572. doi: 10.1073/pnas.1510459112

PubMed Abstract | CrossRef Full Text | Google Scholar

Brown, A. S. (2011). The environment and susceptibility to schizophrenia. Prog. Neurobiol. 93, 23–58. doi: 10.1016/j.pneurobio.2010.09.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Browning, M. H., Shipley, N., McAnirlin, O., Becker, D., Yu, C. P., Hartig, T., et al. (2020). An actual natural setting improves mood better than its virtual counterpart: a meta-analysis of experimental data. Front. Psychol. 11:2200. doi: 10.3389/fpsyg.2020.02200

CrossRef Full Text | Google Scholar

Cohen-Cline, H., Turkheimer, E., and Duncan, G. E. (2015). Access to green space, physical activity and mental health: a twin study. J. Epidemiol. Community Health 69, 523–529. doi: 10.1136/jech-2014-204667

PubMed Abstract | CrossRef Full Text | Google Scholar

Damasio, A. R. (1999). The feeling of what happens: Body and emotion in the making of consciousness. New York: Houghton Mifflin Harcourt.

Google Scholar

Di Plinio, S., Perrucci, M. G., Aleman, A., and Ebisch, S. J. (2020). I am me: brain systems integrate and segregate to establish a multidimensional sense of self. Neuroimage 205:116284. doi: 10.1016/j.neuroimage.2019.116284

PubMed Abstract | CrossRef Full Text | Google Scholar

Dragt, S., Nieman, D. H., Veltman, D., Becker, H. E., van de Fliert, R., de Haan, L., et al. (2011). Environmental factors and social adjustment as predictors of a first psychosis in subjects at ultra high risk. Schizophr. Res. 125, 69–76. doi: 10.1016/j.schres.2010.09.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Ebisch, S. J., and Aleman, A. (2016). The fragmented self: imbalance between intrinsic and extrinsic self-networks in psychotic disorders. Lancet Psychiatry 3, 784–790. doi: 10.1016/S2215-0366(16)00045-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Engemann, K., Pedersen, C. B., Arge, L., Tsirogiannis, C., Mortensen, P. B., and Svenning, J. C. (2018). Childhood exposure to green space – a novel risk-decreasing mechanism for schizophrenia? Schizophr. Res. 199, 142–148. doi: 10.1016/j.schres.2018.03.026

PubMed Abstract | CrossRef Full Text | Google Scholar

Engemann, K., Pedersen, C. B., Arge, L., Tsirogiannis, C., Mortensen, P. B., and Svenning, J. C. (2019a). Residential green space in childhood is associated with lower risk of psychiatric disorders from adolescence into adulthood. Proc. Natl. Acad. Sci. U. S. A. 116, 5188–5193. doi: 10.1073/pnas.1807504116

PubMed Abstract | CrossRef Full Text | Google Scholar

Engemann, K., Svenning, J. C., Arge, L., Brandt, J., Geels, C., Mortensen, P. B., et al. (2019b). Natural surroundings in childhood are associated with lower schizophrenia rates. Schizophr. Res. doi: 10.1016/j.schres.2019.10.012 (in press).

CrossRef Full Text | Google Scholar

Engemann, K., Pedersen, C. B., Agerbo, E., Arge, L., Børglum, A. D., Erikstrup, C., et al. (2020). Association between childhood green space, genetic liability, and the incidence of Schizophrenia. Schizophr. Bull. doi: 10.1093/schbul/sbaa058 [Epub ahead of print]

CrossRef Full Text | Google Scholar

Fazel, S., Wolf, A., Palm, C., and Lichtenstein, P. (2014). Violent crime, suicide, and premature mortality in patients with schizophrenia and related disorders: a 38-year total population study in Sweden. Lancet Psychiatry 1, 44–54. doi: 10.1016/S2215-0366(14)70223-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Frith, C. D., Blakemore, S. J., and Wolpert, D. M. (2000). Explaining the symptoms of schizophrenia: abnormalities in the awareness of action. Brain Res. Brain Res. Rev. 31, 357–363. doi: 10.1016/s0165-0173(99)00052-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Fuller, C., Powell, D., and Fox, S. (2017). Making gains: the impact of outdoor residential experiences on students’ examination grades and self-efficacy. Educ. Rev. 69, 232–247. doi: 10.1080/00131911.2016.1199538

CrossRef Full Text | Google Scholar

Fusar-Poli, P., Davies, C., Solmi, M., Brondino, N., De Micheli, A., Kotlicka-Antczak, M., et al. (2019). Preventive treatments for psychosis: umbrella review (just the evidence). Front. Psychol. 10:764. doi: 10.3389/fpsyt.2019.00764

PubMed Abstract | CrossRef Full Text | Google Scholar

Fusar-Poli, P., Tantardini, M., De Simone, S., Ramella-Cravaro, V., Oliver, D., Kingdon, J., et al. (2017). Deconstructing vulnerability for psychosis: meta-analysis of environmental risk factors for psychosis in subjects at ultra high-risk. Eur. Psychiatry 40, 65–75. doi: 10.1016/j.eurpsy.2016.09.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Gallagher, S. (2000). Philosophical conceptions of the self: implications for cognitive science. Trends Cogn. Sci. 4, 14–21. doi: 10.1016/S1364-6613(99)01417-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Gallese, V., and Sinigaglia, C. (2010). The bodily self as power for action. Neuropsychologia 48, 746–755. doi: 10.1016/j.neuropsychologia.2009.09.038

PubMed Abstract | CrossRef Full Text | Google Scholar

Haggard, P. (2017). Sense of agency in the human brain. Nat. Rev. Neurosci. 18, 196–207. doi: 10.1038/nrn.2017.14

PubMed Abstract | CrossRef Full Text | Google Scholar

Hartig, T. (1993). Nature experience in transactional perspective. Landsc. Urban Plan. 25, 17–36. doi: 10.1016/0169-2046(93)90120-3

CrossRef Full Text | Google Scholar

Hartig, T., Mitchell, R., de Vries, S., and Frumkin, H. (2014). Nature and health. Annu. Rev. Public Health 35, 207–228. doi: 10.1146/annurev-publhealth-032013-182443

CrossRef Full Text | Google Scholar

Hayhurst, J., Hunter, J. A., Kafka, S., and Boyes, M. (2015). Enhancing resilience in youth through a 10-day developmental voyage. J. Adventure Educ. Outdoor Learn. 15, 40–52. doi: 10.1080/14729679.2013.843143

CrossRef Full Text | Google Scholar

Howes, O. D., McDonald, C., Cannon, M., Arseneault, L., Boydell, J., and Murray, R. M. (2004). Pathways to schizophrenia: the impact of environmental factors. Int. J. Neuropsychopharmacol. 7, S7–S13. doi: 10.1017/S1461145704004122

PubMed Abstract | CrossRef Full Text | Google Scholar

Huang, S. C. L. (2009). The validity of visual surrogates for representing waterscapes. Landsc. Res. 34, 323–335. doi: 10.1080/01426390902867984

CrossRef Full Text | Google Scholar

Huang, S. C. L., Chiang, N. C., Kuo, N. F., and Chen, Y. J. (2019). An exploratory approach for using EEG to examine person-environment interaction. Landsc. Res. 44, 702–715. doi: 10.1080/01426397.2018.1548586

CrossRef Full Text | Google Scholar

Hunter, J. A., Kafka, S., Hayhurst, J., Clark, H., Dickerson, D., Harold, G., et al. (2010). Increased self-efficacy following a ten-day developmental voyage. J. Child Adolesc. Ment. Health 22, 63–65. doi: 10.2989/17280583.2010.496943

PubMed Abstract | CrossRef Full Text | Google Scholar

James, W. (1890). Principles of psychology. Vol. 2. New York: Henry Holt and Company, 283–324.

Google Scholar

James, P., Banay, R. F., Hart, J. E., and Laden, F. (2015). A review of the health benefits of greenness. Curr. Epidemiol. Rep. 2, 131–142. doi: 10.1007/s40471-015-0043-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Jeannerod, M. (2003). The mechanism of self-recognition in humans. Behav. Brain Res. 142, 1–15. doi: 10.1016/s0166-4328(02)00384-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Kaplan, R., and Kaplan, S. (1989). The experience of nature: A psychological perspective. New York: Cambridge University Press Archive.

Google Scholar

Kelly, B. D., O’Callaghan, E., Waddington, J. L., Feeney, L., Browne, S., Scully, P. J., et al. (2010). Schizophrenia and the city: a review of literature and prospective study of psychosis and urbanicity in Ireland. Schizophr. Res. 116, 75–89. doi: 10.1016/j.schres.2009.10.015

PubMed Abstract | CrossRef Full Text | Google Scholar

Kircher, T. T., and Leube, D. T. (2003). Self-consciousness, self-agency, and schizophrenia. Conscious. Cogn. 12, 656–669. doi: 10.1016/s1053-8100(03)00071-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Krabbendam, L., and van Os, J. (2005). Schizophrenia and urbanicity: a major environmental influence—conditional on genetic risk. Schizophr. Bull. 31, 795–799. doi: 10.1093/schbul/sbi060

PubMed Abstract | CrossRef Full Text | Google Scholar

Kühn, S., and Gallinat, J. (2013). Resting-state brain activity in schizophrenia and major depression: a quantitative meta-analysis. Schizophr. Bull. 39, 358–365. doi: 10.1093/schbul/sbr151

PubMed Abstract | CrossRef Full Text | Google Scholar

Kuo, M. (2015). How might contact with nature promote human health? Promising mechanisms and a possible central pathway. Front. Psychol. 6:1093. doi: 10.3389/fpsyg.2015.01093

PubMed Abstract | CrossRef Full Text | Google Scholar

Lederbogen, F., Kirsch, P., Haddad, L., Streit, F., Tost, H., Schuch, P., et al. (2011). City living and urban upbringing affect neural social stress processing in humans. Nature 474, 498–501. doi: 10.1038/nature10190

PubMed Abstract | CrossRef Full Text | Google Scholar

Lewis, G., David, A., Andréassson, S., and Allebeck, P. (1992). Schizophrenia and city life. Lancet 340, 137–140. doi: 10.1016/0140-6736(92)93213-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Looijestijn, J., Blom, J. D., Aleman, A., Hoek, H. W., and Goekoop, R. (2015). An integrated network model of psychotic symptoms. Neurosci. Biobehav. Rev. 59, 238–250. doi: 10.1016/j.neubiorev.2015.09.016

PubMed Abstract | CrossRef Full Text | Google Scholar

Maas, J., Verheij, R. A., de Vries, S., Spreeuwenberg, P., Schellevis, F. G., and Groenewegen, P. P. (2009). Morbidity is related to a green living environment. J. Epidemiol. Community Health 63, 967–973. doi: 10.1136/jech.2008.079038

PubMed Abstract | CrossRef Full Text | Google Scholar

Margalit, D., and Ben-Ari, A. (2014). The effect of wilderness therapy on adolescents’ cognitive autonomy and self-efficacy: results of a non-randomized trial. Child Youth Care Forum 43, 181–194. doi: 10.1007/s10566-013-9234-x

CrossRef Full Text | Google Scholar

Markevych, I., Schoierer, J., Hartig, T., Chudnovsky, A., Hystad, P., Dzhambov, A. M., et al. (2017). Exploring pathways linking greenspace to health: theoretical and methodological guidance. Environ. Res. 158, 301–317. doi: 10.1016/j.envres.2017.06.028

PubMed Abstract | CrossRef Full Text | Google Scholar

McGorry, P. D., Nelson, B., Amminger, G. P., Bechdolf, A., Francey, S. M., Berger, G., et al. (2009). Intervention in individuals at ultra-high risk for psychosis: a review and future directions. J. Clin. Psychiatry 70, 1206–1212. doi: 10.4088/JCP.08r04472

PubMed Abstract | CrossRef Full Text | Google Scholar

McGrath, J., Saha, S., Welham, J., El Saadi, O., MacCauley, C., and Chant, D. (2004). A systematic review of the incidence of schizophrenia: the distribution of rates and the influence of sex, urbanicity, migrant status and methodology. BMC Med. 2:13. doi: 10.1186/1741-7015-2-13

PubMed Abstract | CrossRef Full Text | Google Scholar

Menon, V., and Uddin, L. Q. (2010). Saliency, switching, attention and control: a network model of insula function. Brain Struct. Funct. 214, 655–667. doi: 10.1007/s00429-010-0262-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Meyer-Lindenberg, A., and Tost, H. (2012). Neural mechanisms of social risk for psychiatric disorders. Nat. Neurosci. 15, 663–668. doi: 10.1038/nn.3083

PubMed Abstract | CrossRef Full Text | Google Scholar

Minkowski, E. (1927). “La schizophrénie” in Psychopathologie des schizoïdes et des schizophrénes. ed. Payot (Paris).

Google Scholar

Modinos, G., Renken, R., Ormel, J., and Aleman, A. (2011). Self-reflection and the psychosis-prone brain: an fMRI study. Neuropsychology 25, 295–305. doi: 10.1037/a0021747

PubMed Abstract | CrossRef Full Text | Google Scholar

Molnar-Szakacs, I., and Uddin, L. Q. (2013). Self-processing and the default mode network: interactions with the mirror neuron system. Front. Hum. Neurosci. 7:571. doi: 10.3389/fnhum.2013.00571

PubMed Abstract | CrossRef Full Text | Google Scholar

Mygind, L., Kjeldsted, E., Hartmeyer, R., Mygind, E., Bølling, M., and Bentsen, P. (2019). Mental, physical and social health benefits of immersive nature-experience for children and adolescents: a systematic review and quality assessment of the evidence. Health Place 58:102136. doi: 10.1016/j.healthplace.2019.05.014

PubMed Abstract | CrossRef Full Text | Google Scholar

Nelson, B., Fornito, A., Harrison, B. J., Yücel, M., Sass, L. A., Yung, A. R., et al. (2009). A disturbed sense of self in the psychosis prodrome: linking phenomenology and neurobiology. Neurosci. Biobehav. Rev. 33, 807–817. doi: 10.1016/j.neubiorev.2009.01.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Nelson, B., Parnas, J., and Sass, L. A. (2014). Disturbance of minimal self (ipseity) in schizophrenia: clarification and current status. Schizophr. Bull. 40, 479–482. doi: 10.1093/schbul/sbu034

PubMed Abstract | CrossRef Full Text | Google Scholar

Nelson, B., Thompson, A., and Yung, A. R. (2012). Basic self-disturbance predicts psychosis onset in the ultra high risk for psychosis “prodromal” population. Schizophr. Bull. 38, 1277–1287. doi: 10.1093/schbul/sbs007

PubMed Abstract | CrossRef Full Text | Google Scholar

Newbury, J., Arseneault, L., Caspi, A., Moffitt, T. E., Odgers, C. L., and Fisher, H. L. (2016). Why are children in urban neighborhoods at increased risk for psychotic symptoms? Findings from a UK longitudinal cohort study. Schizophr. Bull. 42, 1372–1383. doi: 10.1093/schbul/sbw052

PubMed Abstract | CrossRef Full Text | Google Scholar

Northoff, G. (2017). Personal identity and cortical midline structure (CMS): do temporal features of CMS neural activity transform into “self-continuity”? Psychol. Inq. 28, 122–131. doi: 10.1080/1047840X.2017.1337396

CrossRef Full Text | Google Scholar

Northoff, G., and Bermpohl, F. (2004). Cortical midline structures and the self. Trends Cogn. Sci. 8, 102–107. doi: 10.1016/j.tics.2004.01.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Northoff, G., and Huang, Z. (2017). How do the brain’s time and space mediate consciousness and its different dimensions? Temporo-spatial theory of consciousness (TTC). Neursci. Biobehav. Rev. 80, 630–645. doi: 10.1016/j.neubiorev.2017.07.013

PubMed Abstract | CrossRef Full Text | Google Scholar

Northoff, G., and Panksepp, J. (2008). The trans-species concept of self and the subcortical–cortical midline system. Trends Cogn. Sci. 12, 259–264. doi: 10.1016/j.tics.2008.04.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Northoff, G., Qin, P., and Nakao, T. (2010). Rest-stimulus interaction in the brain: a review. Trends Neurosci. 33, 277–284. doi: 10.1016/j.tins.2010.02.006

PubMed Abstract | CrossRef Full Text | Google Scholar

O’Brien, K., and Lomas, T. (2017). Developing a growth mindset through outdoor personal development: can an intervention underpinned by psychology increase the impact of an outdoor learning course for young people? J. Adventure Educ. Outdoor Learn. 17, 133–147. doi: 10.1080/14729679.2016.1232199

CrossRef Full Text | Google Scholar

Parnas, J., and Henriksen, M. G. (2014). Disordered self in the schizophrenia spectrum: a clinical and research perspective. Harv. Rev. Psychiatry 22, 251–265. doi: 10.1097/HRP.0000000000000040

PubMed Abstract | CrossRef Full Text | Google Scholar

Pedersen, C. B., and Mortensen, P. B. (2001). Evidence of a dose-response relationship between urbanicity during upbringing and schizophrenia risk. Arch. Gen. Psychiatry 58, 1039–1046. doi: 10.1001/archpsyc.58.11.1039

PubMed Abstract | CrossRef Full Text | Google Scholar

Pries, L. K., Guloksuz, S., Ten Have, M., de Graaf, R., van Dorsselaer, S., Gunther, N., et al. (2018). Evidence that environmental and familial risks for psychosis additively impact a multidimensional subthreshold psychosis syndrome. Schizophr. Bull. 44, 710–719. doi: 10.1093/schbul/sby051

PubMed Abstract | CrossRef Full Text | Google Scholar

Qin, P., and Northoff, G. (2011). How is our self related to midline regions and the default-mode network? Neuroimage 57, 1221–1233. doi: 10.1016/j.neuroimage.2011.05.028

PubMed Abstract | CrossRef Full Text | Google Scholar

Raballo, A., Sæbye, D., and Parnas, J. (2011). Looking at the schizophrenia spectrum through the prism of self-disorders: an empirical study. Schizophr. Bull. 37, 344–351. doi: 10.1093/schbul/sbp056

PubMed Abstract | CrossRef Full Text | Google Scholar

Rössler, W., Salize, H. J., van Os, J., and Riecher-Rössler, A. (2005). Size of burden of schizophrenia and psychotic disorders. Eur. Neuropsychopharmacol. 15, 399–409. doi: 10.1016/j.euroneuro.2005.04.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Ruhrmann, S., Schultze-Lutter, F., Salokangas, R. K., Heinimaa, M., Linszen, D., Dingemans, P., et al. (2010). Prediction of psychosis in adolescents and young adults at high risk: results from the prospective European prediction of psychosis study. Arch. Gen. Psychiatry 67, 241–251. doi: 10.1001/archgenpsychiatry.2009.206

PubMed Abstract | CrossRef Full Text | Google Scholar

Sarkar, C., Webster, C., and Gallacher, J. (2018). Residential greenness and prevalence of major depressive disorders: a cross-sectional, observational, associational study of 94 879 adult UK biobank participants. Lancet Planet. Health 2, e162–e173. doi: 10.1016/S2542-5196(18)30051-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Sass, L. A., and Parnas, J. (2003). Schizophrenia, consciousness, and the self. Schizophr. Bull. 29, 427–444. doi: 10.1093/oxfordjournals.schbul.a007017

PubMed Abstract | CrossRef Full Text | Google Scholar

Scalabrini, A., Ebisch, S. J., Huang, Z., Di Plinio, S., Perrucci, M. G., Romani, G. L., et al. (2019). Spontaneous brain activity predicts task-evoked activity during animate versus inanimate touch. Cereb. Cortex 29, 4628–4645. doi: 10.1093/cercor/bhy340

PubMed Abstract | CrossRef Full Text | Google Scholar

Schmitt, A., Malchow, B., Hasan, A., and Fallkai, P. (2014). The impact of environmental factors in severe psychiatric disorders. Front. Neurosci. 8:19. doi: 10.3389/fnins.2014.00019

PubMed Abstract | CrossRef Full Text | Google Scholar

Schultze-Lutter, F. (2009). Subjective symptoms of schizophrenia in research and the clinic: the basic symptom concept. Schizophr. Bull. 35, 5–8. doi: 10.1093/schbul/sbn139

PubMed Abstract | CrossRef Full Text | Google Scholar

Smigielski, L., Jagannath, V., Rössler, W., Walitza, S., and Grünblatt, E. (2020). Epigenetic mechanisms in schizophrenia and other psychotic disorders: a systematic review of empirical human findings. Mol. Psychiatry 25, 1718–1748. doi: 10.1038/s41380-019-0601-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Smith, G., Cirach, M., Swart, W., Dėdelė, A., Gidlow, C., van Kempen, E., et al. (2017). Characterisation of the natural environment: quantitative indicators across Europe. Int. J. Health Geogr. 16:16. doi: 10.1186/s12942-017-0090-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Sundquist, K., Frank, G., and Sundquist, J. A. N. (2004). Urbanisation and incidence of psychosis and depression: follow-up study of 4.4 million women and men in Sweden. Br. J. Psychiatry 184, 293–298. doi: 10.1192/bjp.184.4.293

PubMed Abstract | CrossRef Full Text | Google Scholar

Sussman, A., and Hollander, J. B. (2014). Cognitive architecture: Designing for how we respond to the built environment. New York: Routledge.

Google Scholar

Tan, S., Zhao, Y., Fan, F., Zou, Y., Jin, Z., Zen, Y., et al. (2015). Brain correlates of self-evaluation deficits in schizophrenia: a combined functional and structural MRI study. PLoS One 10:e0138737. doi: 10.1371/journal.pone.0138737

PubMed Abstract | CrossRef Full Text | Google Scholar

Torrey, E. F., and Yolken, R. H. (2019). Schizophrenia as a pseudogenetic disease: a call for more gene-environmental studies. Psychiatry Res. 278, 146–150. doi: 10.1016/j.psychres.2019.06.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Tost, H., Reichert, M., Braun, U., Reinhard, I., Peters, R., Lautenbach, S., et al. (2019). Neural correlates of individual differences in affective benefit of real-life urban green space exposure. Nat. Neurosci. 22, 1389–1393. doi: 10.1038/s41593-019-0451-y

PubMed Abstract | CrossRef Full Text | Google Scholar

Tsuang, M. (2000). Schizophrenia: genes and environment. Biol. Psychiatry 47, 210–220. doi: 10.1016/S0006-3223(99)00289-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Twedt, E., Rainey, R. M., and Proffitt, D. R. (2016). Designed natural spaces: informal gardens are perceived to be more restorative than formal gardens. Front. Psychol. 7:88. doi: 10.3389/fpsyg.2016.00088

PubMed Abstract | CrossRef Full Text | Google Scholar

Twohig-Bennett, C., and Jones, A. (2018). The health benefits of the great outdoors: a systematic review and meta-analysis of greenspace exposure and health outcomes. Environ. Res. 166, 628–637. doi: 10.1016/j.envres.2018.06.030

PubMed Abstract | CrossRef Full Text | Google Scholar

Ulrich, R. S., Simons, R. F., Losito, B. D., Fiorito, E., Miles, M. A., and Zelson, M. (1991). Stress recovery during exposure to natural and urban environments. J. Environ. Psychol. 11, 201–230. doi: 10.1016/S0272-4944(05)80184-7

PubMed Abstract | CrossRef Full Text | Google Scholar

United Nations, Department of Economic and Social Affairs, Population Division (2014). World urbanization prospects: The 2014 revision, highlights (ST/ESA/SER.A/352). Available at: https://esa.un.org/unpd/wup/Publications/Files/WUP2014-Highlights.pdf (Accessed January 30, 2020).

Google Scholar

van den Berg, M., Wendel-Vos, W., van Poppel, M., Kemper, H., van Mechelen, W., and Maas, J. (2015). Health benefits of green spaces in the living environment: a systematic review of epidemiological studies. Urban For. Urban Green. 14, 806–816. doi: 10.1016/j.ufug.2015.07.008

CrossRef Full Text | Google Scholar

van der Meer, L., Costafreda, S., Aleman, A., and David, A. S. (2010). Self-reflection and the brain: a theoretical review and meta-analysis of neuroimaging studies with implications for schizophrenia. Neursci. Biobehav. Rev. 34, 935–946. doi: 10.1016/j.neubiorev.2009.12.004

PubMed Abstract | CrossRef Full Text | Google Scholar

van der Meer, L., de Vos, A. E., Stiekema, A. P., Pijnenborg, G. H., van Tol, M. J., Nolen, W. A., et al. (2013). Insight in schizophrenia: involvement of self-reflection networks? Schizophr. Bull. 39, 1288–1295. doi: 10.1093/schbul/sbs122

PubMed Abstract | CrossRef Full Text | Google Scholar

Vanhaudenhuyse, A., Demertzi, A., Schabus, M., Noirhomme, Q., Bredart, S., Boly, M., et al. (2011). Two distinct neuronal networks mediate the awareness of environment and of self. J. Cogn. Neurosci. 23, 570–578. doi: 10.1162/jocn.2010.21488

PubMed Abstract | CrossRef Full Text | Google Scholar

van Kemenade, B. M., Arikan, B. E., Podranski, K., Steinsträter, O., Kircher, T., and Straube, B. (2019). Distinct roles for the cerebellum, angular gyrus, and middle temporal gyrus in action–feedback monitoring. Cereb. Cortex 29, 1520–1531. doi: 10.1093/cercor/bhy048

PubMed Abstract | CrossRef Full Text | Google Scholar

van Os, J., Kenis, G., and Rutten, B. (2010). The environment and schizophrenia. Nature 468, 203–212. doi: 10.1038/nature09563

PubMed Abstract | CrossRef Full Text | Google Scholar

van Os, J., and Linscott, R. J. (2012). Introduction: the extended psychosis phenotype—relationship with schizophrenia and with ultrahigh risk status for psychosis. Schizophr. Bull. 38, 227–230. doi: 10.1093/schbul/sbr188

PubMed Abstract | CrossRef Full Text | Google Scholar

van Os, J., Pedersen, C. B., and Mortensen, P. B. (2004). Confirmation of synergy between urbanicity and familial liability in the causation of psychosis. Am. J. Psychiatry 161, 2312–2314. doi: 10.1176/appi.ajp.161.12.2312

PubMed Abstract | CrossRef Full Text | Google Scholar

van Os, J., Reininghaus, U., and Meyer-Lindenberg, A. (2017). The search for environmental mechanisms underlying the expression of psychosis: introduction. Schizophr. Bull. 43, 283–286. doi: 10.1093/schbul/sbw178

PubMed Abstract | CrossRef Full Text | Google Scholar

Verheij, R. A., Maas, J., and Groenewegen, P. P. (2008). Urban—rural health differences and the availability of green space. Eur. Urban Reg. Stud. 15, 307–316. doi: 10.1177/0969776408095107

CrossRef Full Text | Google Scholar

Völker, S., and Kistemann, T. (2011). The impact of blue space on human health and well-being–salutogenetic health effects of inland surface waters: a review. Int. J. Hyg. Environ. Health 214, 449–460. doi: 10.1016/j.ijheh.2011.05.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Waters, F., Woodward, T., Allen, P., Aleman, A., and Sommer, I. (2012). Self-recognition deficits in schizophrenia patients with auditory hallucinations: a meta-analysis of the literature. Schizophr. Bull. 38, 741–750. doi: 10.1093/schbul/sbq144

PubMed Abstract | CrossRef Full Text | Google Scholar

White, M. P., Alcock, I., Wheeler, B. W., and Depledge, M. H. (2013). Would you be happier living in a greener urban area? A fixed-effects analysis of panel data. Psychol. Sci. 24, 920–928. doi: 10.1177/0956797612464659

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: intrinsic self, extrinsic self, environment, green space, natural surroundings, psychosis, schizophrenia, urban

Citation: Ebisch SJH (2020) The Self and Its Nature: A Psychopathological Perspective on the Risk-Reducing Effects of Environmental Green Space for Psychosis. Front. Psychol. 11:531840. doi: 10.3389/fpsyg.2020.531840

Received: 01 February 2020; Accepted: 21 October 2020;
Published: 11 November 2020.

Edited by:

Giuseppina Spano, University of Bari Aldo Moro, Italy

Reviewed by:

Annalisa Theodorou, Roma Tre University, Italy
Simon Bell, University of Edinburgh, United Kingdom

Copyright © 2020 Ebisch. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Sjoerd J. H. Ebisch, cy5lYmlzY2hAdW5pY2guaXQ=

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.