Dear Liz,
sorry for the slow response,
I guess the failure of the PDF printing may be due to a buffer/memory overrun. How many loci and populations do you run?
Your parmfile contains a few small things that I would change:
without replication, these options:
gelman-convergence=YES:SUM
is not doing anything; the use of the convergence measure is brittle in that it often does not really work. I suggest running the program a few times and comparing the parameter estimates. I usually increase the long-inc by a factor of 5x or 10x if the results are stable; I assume convergence was fine.
change
long-chains=3
to
long-chains=1 #3 will not do anything; I need to remove this option as it is not functional anymore
experiment with 100, 500, 1000 (see above)
long-inc=100
geo=YES:geofile.txt
often this does not seem to be needed, as you want the geneflow between locations and not geneflow scaled by distance per location
mutation=DATA
if you have sequence data, I would set this CONSTANT, as this will make it easier to compare your parameter values per locus, as they are all scaled by the same mutation rate
mig-histogram=ALL:0.001:mighistfile
skyline=YES:0.001:skylinefile
Without dated tips, these are often poorly estimated; I suggest not using them in early runs (or not at all)
pdf-terse=NO
if you have 1000s of loci, consider using
pdf-terse=YES
this reduces the size of the report data table, etc
best
Peter