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# Line 337 | Line 337 | distribution,
337   connected to the Hamiltonian $H$ through Maxwell-Boltzmann
338   distribution,
339   \begin{equation}
340 < \rho  \propto e^{ - \beta H}
340 > \rho  \propto e^{ - \beta H}.
341   \label{introEquation:densityAndHamiltonian}
342   \end{equation}
343  
# Line 349 | Line 349 | inside this region is given by,
349   If this region is small enough, the density $\rho$ can be regarded
350   as uniform over the whole integral. Thus, the number of phase points
351   inside this region is given by,
352 < \begin{equation}
353 < \delta N = \rho \delta v = \rho \int { \ldots \int {dq_1 } ...dq_f
354 < dp_1 } ..dp_f.
355 < \end{equation}
356 <
357 < \begin{equation}
358 < \frac{{d(\delta N)}}{{dt}} = \frac{{d\rho }}{{dt}}\delta v + \rho
352 > \begin{eqnarray}
353 > \delta N &=& \rho \delta v = \rho \int { \ldots \int {dq_1 } ...dq_f dp_1 } ..dp_f,\\
354 > \frac{{d(\delta N)}}{{dt}} &=& \frac{{d\rho }}{{dt}}\delta v + \rho
355   \frac{d}{{dt}}(\delta v) = 0.
356 < \end{equation}
356 > \end{eqnarray}
357   With the help of the stationary assumption
358   (Eq.~\ref{introEquation:stationary}), we obtain the principle of
359   \emph{conservation of volume in phase space},
# Line 466 | Line 462 | Given vector spaces $V$ and $W$ over same field $F$, $
462   \lambda_2\omega(x_2, y)$, $\omega(x, y) = - \omega(y, x)$ and
463   $\omega(x, x) = 0$.\cite{McDuff1998} The cross product operation in
464   vector field is an example of symplectic form.
465 < Given vector spaces $V$ and $W$ over same field $F$, $f: V \to W$ is a linear transformation if
465 > Given vector spaces $V$ and $W$ over same field $F$, $f: V \to W$ is a linear transformation if
466   \begin{eqnarray*}
467   f(x+y) & = & f(x) + f(y) \\
468 < f(ax) & = & af(x)      
468 > f(ax) & = & af(x)
469   \end{eqnarray*}
470   are always satisfied for any two vectors $x$ and $y$ in $V$ and any scalar $a$ in $F$. One can define the dual vector space $V^*$ of $V$ if any two built-in linear transformations $\phi$ and $\psi$ in $V^*$ satisfy the following definition of addition and scalar multiplication:
471   \begin{eqnarray*}
# Line 478 | Line 474 | for all $a$ in $F$ and $x$ in $V$. For a manifold $M$,
474   \end{eqnarray*}
475   for all $a$ in $F$ and $x$ in $V$. For a manifold $M$, one can define a tangent vector of a tangent space $TM_q$ at every point $q$
476   \begin{equation}
477 < \dot q = \mathop {\lim }\limits_{t \to 0} \frac{{\phi (t) - \phi (0)}}{t}      
477 > \dot q = \mathop {\lim }\limits_{t \to 0} \frac{{\phi (t) - \phi (0)}}{t}
478   \end{equation}
479   where $\phi(0)=q$ and $\phi(t) \in M$. One may also define a cotangent space $T^*M_q$ as the dual space of the tangent space $TM_q$. The tangent space and the cotangent space are isomorphic to each other, since they are both real vector spaces with same dimension.
480 < The union of tangent spaces at every point of $M$ is called the tangent bundle of $M$ and is denoted by $TM$, while cotangent bundle $T^*M$ is defined as the union of the cotangent spaces to $M$.\cite{Jost2002} For a Hamiltonian system with configuration manifold $V$, the $(q,\dot q)$ phase space is the tangent bundle of the configuration manifold $V$, while the cotangent bundle is represented by $(q,p)$.
480 > The union of tangent spaces at every point of $M$ is called the tangent bundle of $M$ and is denoted by $TM$, while cotangent bundle $T^*M$ is defined as the union of the cotangent spaces to $M$.\cite{Jost2002} For a Hamiltonian system with configuration manifold $V$, the $(q,\dot q)$ phase space is the tangent bundle of the configuration manifold $V$, while the cotangent bundle is represented by $(q,p)$.
481  
482   \subsection{\label{introSection:ODE}Ordinary Differential Equations}
483  
# Line 992 | Line 988 | illustration of shifted Coulomb potential.}
988   illustration of shifted Coulomb potential.}
989   \label{introFigure:shiftedCoulomb}
990   \end{figure}
995
996 %multiple time step
991  
992   \subsection{\label{introSection:Analysis} Analysis}
993  
994 < Recently, advanced visualization techniques have been applied to
1001 < monitor the motions of molecules. Although the dynamics of the
1002 < system can be described qualitatively from animation, quantitative
1003 < trajectory analysis is more useful. According to the principles of
994 > According to the principles of
995   Statistical Mechanics in
996   Sec.~\ref{introSection:statisticalMechanics}, one can compute
997   thermodynamic properties, analyze fluctuations of structural
# Line 1258 | Line 1249 | equation of motion for angular momentum in the body fr
1249   motion. This unique property eliminates the requirement of
1250   iterations which can not be avoided in other methods.\cite{Kol1997,
1251   Omelyan1998} Applying the hat-map isomorphism, we obtain the
1252 < equation of motion for angular momentum in the body frame
1252 > equation of motion for angular momentum
1253   \begin{equation}
1254   \dot \pi  = \pi  \times I^{ - 1} \pi  + \sum\limits_i {\left( {Q^T
1255   F_i (r,Q)} \right) \times X_i }.
# Line 1629 | Line 1620 | and Eq.~\ref{introEuqation:GeneralizedLangevinDynamics
1620   \int_0^t {\xi (t)\dot x(t - \tau )d\tau }  = 2\xi _0 \int_0^t
1621   {\delta (t)\dot x(t - \tau )d\tau }  = \xi _0 \dot x(t),
1622   \]
1623 < and Eq.~\ref{introEuqation:GeneralizedLangevinDynamics} becomes
1623 > and Eq.~\ref{introEuqation:GeneralizedLangevinDynamics} becomes the
1624 > Langevin equation
1625   \begin{equation}
1626   m\ddot x =  - \frac{{\partial W(x)}}{{\partial x}} - \xi _0 \dot
1627 < x(t) + R(t) \label{introEquation:LangevinEquation}
1627 > x(t) + R(t) \label{introEquation:LangevinEquation}.
1628   \end{equation}
1629 < which is known as the Langevin equation. The static friction
1630 < coefficient $\xi _0$ can either be calculated from spectral density
1631 < or be determined by Stokes' law for regular shaped particles. A
1632 < brief review on calculating friction tensors for arbitrary shaped
1633 < particles is given in Sec.~\ref{introSection:frictionTensor}.
1629 > The static friction coefficient $\xi _0$ can either be calculated
1630 > from spectral density or be determined by Stokes' law for regular
1631 > shaped particles. A brief review on calculating friction tensors for
1632 > arbitrary shaped particles is given in
1633 > Sec.~\ref{introSection:frictionTensor}.
1634  
1635   \subsubsection{\label{introSection:secondFluctuationDissipation}\textbf{The Second Fluctuation Dissipation Theorem}}
1636  

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