diff --git a/BSEdyn.tex b/BSEdyn.tex
index 373dab6..e0deb5b 100644
--- a/BSEdyn.tex
+++ b/BSEdyn.tex
@@ -1023,7 +1023,7 @@ A clear general trend is the consistent red shift of the static BSE excitation e
 \begin{figure*}
 	\includegraphics[width=\linewidth]{fig1a}
 	\includegraphics[width=\linewidth]{fig1b}
-	\caption{Error (in eV) with respect to the TBEs of Refs.~\onlinecite{Loos_2018a,Loos_2019,Loos_2020b} for singlet (top) and triplet (bottom) excitation energies of various molecules obtained with the aug-cc-pVTZ basis set computed within the static (white) and dynamic (colored) BSE formalism. 
+	\caption{Error (in eV) with respect to the TBEs of Refs.~\onlinecite{Loos_2018a,Loos_2019,Loos_2020b} for singlet (top) and triplet (bottom) excitation energies of various molecules obtained with the aug-cc-pVTZ basis set computed within the static (red) and dynamic (blue) BSE formalism. 
 	CT and R stand for charge transfer and Rydberg state, respectively.
 	See Tables \ref{tab:BigTabSi} and \ref{tab:BigTabTr} for raw data.
 	\label{fig:SiTr-SmallMol}}
@@ -1097,7 +1097,7 @@ However, it is definitely an improvement in terms of performances as compared to
 %%% FIG II %%%
 \begin{figure*}
 	\includegraphics[width=\linewidth]{fig2}
-	\caption{Error (in eV) with respect to CC3 for singlet and triplet excitation energies of various molecules obtained with the aug-cc-pVDZ basis set computed within the static (white) and dynamic (colored) BSE formalism. 
+	\caption{Error (in eV) with respect to CC3 for singlet and triplet excitation energies of various molecules obtained with the aug-cc-pVDZ basis set computed within the static (red) and dynamic (blue) BSE formalism. 
 	R stands for Rydberg state.
 	See Table \ref{tab:BigMol} for raw data.
 	\label{fig:SiTr-BigMol}}