Buyukdagli Sahin, Joyeux Marc
Laboratoire de Spectrométrie Physique (CNRS UMR 5588), Université Joseph Fourier, BP 87, 38402 St Martin d'Hères, France.
Phys Rev E Stat Nonlin Soft Matter Phys. 2006 May;73(5 Pt 1):051910. doi: 10.1103/PhysRevE.73.051910. Epub 2006 May 19.
We used the transfer-integral method to compute, with an uncertainty smaller than 5%, the six fundamental characteristic exponents of two dynamical models for DNA thermal denaturation and investigate the validity of the scaling laws. Doubts concerning this point arise because the investigated systems (i) have a divergent internal length, (ii) are described by a divergent order parameter, and (iii) are of dimension 1. We found that the assumption that the free energy can be described by a single homogeneous function is robust, despite the divergence of the order parameter, so that Rushbrooke's and Widom's identities are valid relations. Josephson's identity is instead not satisfied. This is probably due to the divergence of the internal length, which invalidates the assumption that the correlation length is solely responsible for singular contributions to thermodynamic quantities. Fisher's identity is even more wrong. We showed that this is due to the d=1 dimensionality and obtained an alternative law, which is well satisfied at DNA thermal denaturation.
我们使用转移积分法,以小于5%的不确定性计算了两个DNA热变性动力学模型的六个基本特征指数,并研究了标度律的有效性。关于这一点存在疑问,是因为所研究的系统:(i) 具有发散的内禀长度;(ii) 由发散的序参量描述;(iii) 是一维的。我们发现,尽管序参量发散,但自由能可由单个齐次函数描述这一假设是可靠的,因此拉什布鲁克恒等式和维登恒等式是有效的关系。相反,约瑟夫森恒等式不成立。这可能是由于内禀长度的发散,这使得关联长度是热力学量奇异贡献的唯一原因这一假设无效。费希尔恒等式甚至更不准确。我们表明这是由于d = 1维性,并得到了一个替代定律,该定律在DNA热变性时得到了很好的满足。