K. Jaffe, Gerardo L. Febres
{"title":"Defining synergy thermodynamically using quantitative measurements of entropy and free energy","authors":"K. Jaffe, Gerardo L. Febres","doi":"10.1002/cplx.21800","DOIUrl":null,"url":null,"abstract":"Synergy is often defined as the creation of a whole that is greater than the sum of its parts. It is found at all levels of organization in physics, chemistry, biology, social sciences, and the arts. Synergy occurs in open irreversible thermodynamic systems making it difficult to quantify. Negative entropy or negentropy ( N) has been related to order and complexity, and so has work efficiency, information content, Gibbs Free Energy in equilibrium thermodynamics, and useful work efficiency in general ( W). To define synergy in thermodynamic terms, we use the quantitative estimates of changes in N and W in seven different systems that suffer process described as synergistic. The results show that synergistic processes are characterized by an increase in N coupled to an increase in W. Processes not associated to synergy show a different pattern. The opposite of synergy are dissipative processes such as combustion where both N and W decrease. The synergistic processes studied showed a relatively greater increase in N compared to W opening ways to quantify energy—or information—dissipation due to the second law of thermodynamics in open irreversible systems. As a result, we propose a precise thermodynamic definition of synergy and show the potential of thermodynamic measurements in identifying, classifying and analysing in detail synergistic processes. © 2016 Wiley Periodicals, Inc. Complexity 21: 235–242, 2016","PeriodicalId":72654,"journal":{"name":"Complex psychiatry","volume":"97 1","pages":"235-242"},"PeriodicalIF":0.0000,"publicationDate":"2016-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"12","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Complex psychiatry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/cplx.21800","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 12
用熵和自由能的定量测量从热力学角度定义协同作用
协同作用通常被定义为创造一个大于各部分之和的整体。它存在于物理、化学、生物、社会科学和艺术等各个层次的组织中。协同作用发生在开放的不可逆热力学系统中,因此难以量化。负熵或负熵(N)与秩序和复杂性有关,也与功效率、信息含量、平衡热力学中的吉布斯自由能和一般的有用功效率(W)有关。为了从热力学术语中定义协同作用,我们使用了七个不同系统中N和W变化的定量估计,这些系统经历了被称为协同作用的过程。结果表明,协同过程的特征是N的增加耦合到w的增加,而与协同无关的过程则表现出不同的模式。与协同作用相反的是耗散过程,如燃烧,其中N和W都减少。研究的协同过程显示,与W相比,N的增加相对更大,这是由于开放不可逆系统的热力学第二定律导致的。因此,我们提出了协同作用的精确热力学定义,并展示了热力学测量在识别、分类和详细分析协同过程中的潜力。©2016 Wiley期刊公司中文信息学报(英文版),2016
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