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author | Jaron Kent-Dobias <jaron@kent-dobias.com> | 2023-03-06 15:46:02 +0100 |
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committer | Jaron Kent-Dobias <jaron@kent-dobias.com> | 2023-03-06 15:46:02 +0100 |
commit | 58c5055d9e83f3345b90e8c089355c89d362fd57 (patch) | |
tree | 6e0c740dd6eeeec0a7d0ebeff1072397e5a7d4d3 | |
parent | 3debbbe294e0f0c578a337d8bd32a62c37399e17 (diff) | |
download | PRE_107_064111-58c5055d9e83f3345b90e8c089355c89d362fd57.tar.gz PRE_107_064111-58c5055d9e83f3345b90e8c089355c89d362fd57.tar.bz2 PRE_107_064111-58c5055d9e83f3345b90e8c089355c89d362fd57.zip |
Some figure changes for PRE.
-rw-r--r-- | figs/24_opt_dx.pdf | bin | 36864 -> 36861 bytes | |||
-rw-r--r-- | figs/24_opt_qx.pdf | bin | 37774 -> 37780 bytes | |||
-rw-r--r-- | figs/24_opt_rx.pdf | bin | 37311 -> 37316 bytes | |||
-rw-r--r-- | figs/24_opt_xMax.pdf | bin | 39557 -> 41252 bytes | |||
-rw-r--r-- | frsb_kac-rice.bib | 2 | ||||
-rw-r--r-- | frsb_kac-rice.tex | 26 |
6 files changed, 15 insertions, 13 deletions
diff --git a/figs/24_opt_dx.pdf b/figs/24_opt_dx.pdf Binary files differindex a9606fe..c2946c3 100644 --- a/figs/24_opt_dx.pdf +++ b/figs/24_opt_dx.pdf diff --git a/figs/24_opt_qx.pdf b/figs/24_opt_qx.pdf Binary files differindex c884247..fe47e57 100644 --- a/figs/24_opt_qx.pdf +++ b/figs/24_opt_qx.pdf diff --git a/figs/24_opt_rx.pdf b/figs/24_opt_rx.pdf Binary files differindex 502fe5e..fcf5eb4 100644 --- a/figs/24_opt_rx.pdf +++ b/figs/24_opt_rx.pdf diff --git a/figs/24_opt_xMax.pdf b/figs/24_opt_xMax.pdf Binary files differindex c56f296..7fc5ba0 100644 --- a/figs/24_opt_xMax.pdf +++ b/figs/24_opt_xMax.pdf diff --git a/frsb_kac-rice.bib b/frsb_kac-rice.bib index b11ad6c..704d9fd 100644 --- a/frsb_kac-rice.bib +++ b/frsb_kac-rice.bib @@ -443,7 +443,7 @@ stochastic localization}, url = {https://tel.archives-ouvertes.fr/tel-02883385}, hal_id = {tel-02883385}, hal_version = {v1}, - school = {Université Paris-Saclay & Università degli studi La Sapienza (Rome)}, + school = {Université Paris-Saclay \& Università degli studi La Sapienza (Rome)}, type = {Theses} } diff --git a/frsb_kac-rice.tex b/frsb_kac-rice.tex index 3d59148..1d9b33c 100644 --- a/frsb_kac-rice.tex +++ b/frsb_kac-rice.tex @@ -999,8 +999,8 @@ replica symmetry breaking when minima or inherent states do not. \includegraphics[width=\textwidth]{figs/316_complexity.pdf} \caption{ - Complexity of dominant saddles (blue), marginal minima (yellow), and - dominant minima (green) of the $3+16$ model. Solid lines show the result of + Complexity of dominant saddles, marginal minima, and + dominant minima of the $3+16$ model. Solid lines show the result of the 1RSB ansatz, while the dashed lines show that of a RS ansatz. The complexity of marginal minima is always below that of dominant critical points except at the black dot, where they are dominant. @@ -1018,9 +1018,9 @@ replica symmetry breaking when minima or inherent states do not. \caption{ Complexity of the $3+16$ model in the energy $E$ and stability $\mu^*$ - plane. The right shows a detail of the left. Below the yellow marginal line + plane. The right shows a detail of the left. Below the horizontal marginal line the complexity counts saddles of increasing index as $\mu^*$ decreases. - Above the yellow marginal line the complexity counts minima of increasing + Above the horizontal marginal line the complexity counts minima of increasing stability as $\mu^*$ increases. } \label{fig:2rsb.contour} \end{figure} @@ -1049,10 +1049,11 @@ model stall in a place where minima are exponentially subdominant. \caption{ Detail of the `phases' of the $3+16$ model complexity as a function of - energy and stability. Above the yellow marginal stability line the + energy and stability. Above the horizontal marginal stability line the complexity counts saddles of fixed index, while below that line it counts - minima of fixed stability. The shaded red region shows places where the - complexity is described by the 1RSB solution, while the shaded gray region + minima of fixed stability. The shaded red region to the left of the + transition line shows places where the complexity is described by the 1RSB + solution, while the shaded gray region to the right of the transition line shows places where the complexity is described by the RS solution. In white regions the complexity is zero. Several interesting energies are marked with vertical black lines: the traditional `threshold' $E_\mathrm{th}$ @@ -1060,8 +1061,8 @@ model stall in a place where minima are exponentially subdominant. $E_\mathrm{alg}$ that bounds the performance of smooth algorithms, and the average energies at the $2$RSB and $1$RSB equilibrium transitions $\langle E\rangle_2$ and $\langle E\rangle_1$, respectively. Though the figure is - suggestive, $E_\mathrm{alg}$ lies at slightly lower energy than the termination of the RS - -- 1RSB transition line. + suggestive, $E_\mathrm{alg}$ lies at slightly lower energy than the + termination of the RS -- 1RSB transition line. } \label{fig:2rsb.phases} \end{figure} @@ -1160,9 +1161,10 @@ insight into lower-energy symmetry breaking in more general contexts. \includegraphics[width=\textwidth]{figs/24_phases.pdf} \caption{ `Phases' of the complexity for the $2+4$ model in the energy $E$ and - stability $\mu^*$ plane. The region shaded gray shows where the RS solution - is correct, while the region shaded red shows that where the FRSB solution - is correct. The white region shows where the complexity is zero. + stability $\mu^*$ plane. The region shaded gray to the right of the + transition line shows where the RS solution is correct, while the region + shaded red to the left of the transition line shows that where the FRSB + solution is correct. The white region shows where the complexity is zero. } \label{fig:frsb.phases} \end{figure} |