Відмінності між версіями «N Psychophysiology. Lewin, K. (1936). Principles of Topological Psychology. New York, NY»

Матеріал з HistoryPedia
Перейти до: навігація, пошук
м
м
 
Рядок 1: Рядок 1:
Behavior matching in multimodal communication is synchronized. Cogn. Sci. Metzing, C., and Brennan, S. (2003). When conceptual pacts are broken: partner-specific effects around the comprehension of referring expressions. J. Mem. Lang. 49, 201?13. Nadig, A., and [http://community.cosmicradio.tv/discussion/400561/select-this-frames-the-decision-in-a-way-that-biases-participants Select. This frames the decision in a way that biases participants] Sedivy, J. (2002). Proof of perspective-taking constraints in children's on-line reference resolution. Psychol. Sci. 13, 329?36. Navon, D. (1977). Forest before trees: the precedence of international characteristics in visual perception. Cogn. Psychol. 9, 353?83. Norris, C. J., Chen, E. E., Zhu, D. Behavior matching in multimodal communication is synchronized. Cogn. Sci. Metzing, C., and Brennan, S. (2003). When conceptual pacts are broken: partner-specific effects around the comprehension of referring expressions. J. Mem. Lang. 49, 201?13. Nadig, A., and Sedivy, J. (2002). Proof of perspective-taking constraints in children's on-line reference resolution. Psychol. Sci. 13, 329?36. Navon, D. (1977). Forest ahead of trees: the precedence of worldwide functions in visual perception. Cogn. Psychol. 9, 353?83. Norris, C. J., Chen, E. E., Zhu, D. C., Smaller, S. L., and Cacioppo, J. T. (2004). The interaction of social and emotional processes in the brain. J. Cogn. Neurosci. 16, 1818?829. Obhi, S. S., and Sebanz, N. (2011). Moving with each other: toward understanding the mechanisms of joint action. Exp. Brain Res. 211, 329?36. Richardson, D. C., and Dale, R. (2005). Seeking to recognize:
+
Nadig, A., and Sedivy, J. (2002). Proof of perspective-taking constraints in children's on-line reference resolution. [https://www.medchemexpress.com/GSK2656157.html GSK2656157] Psychol. Sci. 13, 329?36. Navon, D. (1977). Forest ahead of trees: the precedence of international attributes in visual perception. Cogn. Psychol. 9, 353?83. Norris, C. J., Chen, E. E., Zhu, D. C., Tiny, S. L., and Cacioppo, J. T. (2004). The interaction of social and emotional processes within the brain. J. Cogn. Neurosci. 16, 1818?829. Obhi, S. S., and Sebanz, N. (2011). Moving with each other: toward understanding the mechanisms of joint action. Even though previous study has recommended that specific factors--such as similarity to the target and familiarity with an experience--can trigger empathy (Preston and De Waal, 2002; Mitchell et al., 2006; Xu et al., 2009), really little investigation has examined how interest impacts our potential to empathize. Previous study suggests that empathy may happen instantaneously and automatically when we recognize another's emotional state (Preston and De Waal, 2002), even if we are cognitively busy. On the other hand, other research suggests that empathy is disrupted when we are distracted and cognitively occupied (Gu and Han, 2007). Simply because attentional sources are typically depleted during daily interactions, it is actually significant to understand if empathy is automatically engaged or calls for controlled and effortful processing. Thus, the present study examines the part of automaticity and focus in neural processes underlying empathy.CORE NEURAL REGIONS FOR EMPATHYA essential purpose to look at empathy for many feelings below several different attentional situations is that it makes it possible for for an analysisof core neural regions for empathy. Earlier analysis has identified neural regions which might be regularly activated for the duration of empathy for physical pain (i.e., dorsal anterior cingulate cortex, dACC; and anterior insula, AI) (Morrison et al., 2004; Singer et al., 2004; Botvinick et al., 2005; Jackson et al., 2005; Zaki et al., 2007; Xu et al., 2009; Lamm et al., 2011). These dependable activations within the dACC and AI have led some researchers to conclude that these regions are part of a core network in empathy (Fan et al., 2011). Nevertheless, it's unknown no matter whether the dACC and AI are necessary to empathic processes additional normally (i.e., not just empathy for pain) and whether or not these regions are activated through empathy for each optimistic and adverse feelings. Current neuroimaging investigation suggests that other neural regions--such because the [https://www.medchemexpress.com/GSK2656157.html GSK2656157 web] medial prefrontal cortex (MPFC; BA 10), dorsomedial prefrontal cortex (DMPFC; BA 9), and ventromedial prefrontal cortex (VMPFC; BA 11)--may be involved in empathic processes.N Psychophysiology. Lewin, K. (1936). A., Bard, E. G. and Jeuniaux, P. (in press). Behavior matching in multimodal communication is synchronized. Cogn. Sci. Psychol. Sci. 13, 329?36. Navon, D. (1977). Forest ahead of trees: the precedence of worldwide attributes in visual perception. Cogn. Psychol. 9, 353?83. Norris, C. J., Chen, E. E., Zhu, D. C., Little, S. L., and Cacioppo, J. T. (2004). The interaction of social and emotional processes in the brain. J. Cogn. Neurosci. 16, 1818?829. Obhi, S. S., and Sebanz, N. (2011). Moving together: toward understanding the mechanisms of joint action. Exp. Brain Res. 211, 329?36. Richardson, D.
Empathy permits us to know and share others' emotions, making a bridge among the self along with the innermost experiences of one more person. As we interact with other people in our every day lives, we might respond empathically to a single individual, but fail to connect with how an additional particular person is feeling. While previous research has suggested that specific factors--such as similarity for the target and familiarity with an experience--can trigger empathy (Preston and De Waal, 2002; Mitchell et al., 2006; Xu et al., 2009), incredibly small analysis has examined how focus impacts our potential to empathize. Past research suggests that empathy may perhaps happen instantaneously and automatically when we recognize another's emotional state (Preston and De Waal, 2002), even though we're cognitively busy. Nevertheless, other investigation suggests that empathy is disrupted when we're distracted and cognitively occupied (Gu and Han, 2007). Simply because attentional sources are normally depleted throughout daily interactions, it can be important to understand if empathy is automatically engaged or needs controlled and effortful processing. Thus, the present study examines the function of automaticity and attention in neural processes underlying empathy.CORE NEURAL REGIONS FOR EMPATHYA crucial reason to appear at empathy for various emotions beneath a variety of attentional situations is that it allows for an analysisof core neural regions for empathy. Earlier research has identified neural regions which can be consistently activated throughout empathy for physical discomfort (i.e., dorsal anterior cingulate cortex, dACC; and anterior insula, AI) (Morrison et al., 2004; Singer et al., 2004; Botvinick et al., 2005; Jackson et al., 2005; Zaki et al., 2007; Xu et al., 2009; Lamm et al., 2011). These trusted activations in the dACC and AI have led some researchers to conclude that these regions are a part of a core network in empathy (Fan et al., 2011).
+

Поточна версія на 12:44, 9 вересня 2017

Nadig, A., and Sedivy, J. (2002). Proof of perspective-taking constraints in children's on-line reference resolution. GSK2656157 Psychol. Sci. 13, 329?36. Navon, D. (1977). Forest ahead of trees: the precedence of international attributes in visual perception. Cogn. Psychol. 9, 353?83. Norris, C. J., Chen, E. E., Zhu, D. C., Tiny, S. L., and Cacioppo, J. T. (2004). The interaction of social and emotional processes within the brain. J. Cogn. Neurosci. 16, 1818?829. Obhi, S. S., and Sebanz, N. (2011). Moving with each other: toward understanding the mechanisms of joint action. Even though previous study has recommended that specific factors--such as similarity to the target and familiarity with an experience--can trigger empathy (Preston and De Waal, 2002; Mitchell et al., 2006; Xu et al., 2009), really little investigation has examined how interest impacts our potential to empathize. Previous study suggests that empathy may happen instantaneously and automatically when we recognize another's emotional state (Preston and De Waal, 2002), even if we are cognitively busy. On the other hand, other research suggests that empathy is disrupted when we are distracted and cognitively occupied (Gu and Han, 2007). Simply because attentional sources are typically depleted during daily interactions, it is actually significant to understand if empathy is automatically engaged or calls for controlled and effortful processing. Thus, the present study examines the part of automaticity and focus in neural processes underlying empathy.CORE NEURAL REGIONS FOR EMPATHYA essential purpose to look at empathy for many feelings below several different attentional situations is that it makes it possible for for an analysisof core neural regions for empathy. Earlier analysis has identified neural regions which might be regularly activated for the duration of empathy for physical pain (i.e., dorsal anterior cingulate cortex, dACC; and anterior insula, AI) (Morrison et al., 2004; Singer et al., 2004; Botvinick et al., 2005; Jackson et al., 2005; Zaki et al., 2007; Xu et al., 2009; Lamm et al., 2011). These dependable activations within the dACC and AI have led some researchers to conclude that these regions are part of a core network in empathy (Fan et al., 2011). Nevertheless, it's unknown no matter whether the dACC and AI are necessary to empathic processes additional normally (i.e., not just empathy for pain) and whether or not these regions are activated through empathy for each optimistic and adverse feelings. Current neuroimaging investigation suggests that other neural regions--such because the GSK2656157 web medial prefrontal cortex (MPFC; BA 10), dorsomedial prefrontal cortex (DMPFC; BA 9), and ventromedial prefrontal cortex (VMPFC; BA 11)--may be involved in empathic processes.N Psychophysiology. Lewin, K. (1936). A., Bard, E. G. and Jeuniaux, P. (in press). Behavior matching in multimodal communication is synchronized. Cogn. Sci. Psychol. Sci. 13, 329?36. Navon, D. (1977). Forest ahead of trees: the precedence of worldwide attributes in visual perception. Cogn. Psychol. 9, 353?83. Norris, C. J., Chen, E. E., Zhu, D. C., Little, S. L., and Cacioppo, J. T. (2004). The interaction of social and emotional processes in the brain. J. Cogn. Neurosci. 16, 1818?829. Obhi, S. S., and Sebanz, N. (2011). Moving together: toward understanding the mechanisms of joint action. Exp. Brain Res. 211, 329?36. Richardson, D.