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dimitri |
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% cd ~/mitgcm/bbl/MITgcm |
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% compare baseline, downslope, and bbl |
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for ts=216:216:21600 |
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s1=35+readbin(['run/SALTanom.' myint2str(ts,10) '.data'],[25 15 25]); |
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s2=35+readbin(['run.down_slope/SALTanom.' myint2str(ts,10) '.data'],[25 15 25]); |
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s3=35+readbin(['run.bbl/SALTanom.' myint2str(ts,10) '.data'],[25 15 25]); |
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clf, subplot(311) |
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mypcolor(1:15,25:-1:1,squeeze(s1(10,:,:))'); |
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caxis([30 30.1]), thincolorbar |
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title(['baseline salinity section on day ' int2str(ts*1200/60/60/24)]) |
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subplot(312) |
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mypcolor(1:15,25:-1:1,squeeze(s2(10,:,:))'); |
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caxis([30 30.1]), thincolorbar |
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title(['downslope salinity section on day ' int2str(ts*1200/60/60/24)]) |
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subplot(313) |
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mypcolor(1:15,25:-1:1,squeeze(s3(10,:,:))'); |
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caxis([30 30.1]), thincolorbar |
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title(['bbl salinity section on day ' int2str(ts*1200/60/60/24)]) |
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pause(.1) |
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end |
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%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% |
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% look at some diagnostics from bbl integration |
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kbot=ones(25,15); |
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s1=35+readbin(['run.bbl/SALTanom.' myint2str(216,10) '.data'],[25 15 25]); |
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for k=2:25 |
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kbot(find(s1(:,:,k)>0))=k; |
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end |
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for ts=216:216:21600 |
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s1=35+readbin(['run.bbl/SALTanom.' myint2str(ts,10) '.data'],[25 15 25]); |
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clf, subplot(321), caxis([30 30.1]), mypcolor(1:15,25:-1:1,squeeze(s1(10,:,:))'); |
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caxis([30 30.1]), thincolorbar |
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title(['salinity section on day ' int2str(ts*1200/60/60/24)]) |
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s2=kbot; for i=1:25, for j=1:15, s2(i,j)=s1(i,j,kbot(i,j)); end, end |
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subplot(322), mypcolor(s2'); caxis([30 30.1]), thincolorbar |
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title('salinity at bottom grid') |
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s3=readbin(['run.bbl/BBLsalt.' myint2str(ts,10) '.data'],[25 15]); |
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subplot(323), mypcolor(s3'); caxis([30 30.1]), thincolorbar |
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title('bbl salinity') |
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subplot(324), mypcolor(s3'-s2'); thincolorbar |
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title('bbl salinity minus bottom salinity') |
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ts=readbin(['run.bbl/BBLtendS.' myint2str(ts,10) '.data'],[25 15]); |
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subplot(325), mypcolor(ts'); thincolorbar |
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title('salinity tendency'), pause(.1) |
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end |