The samples were 1x1x5 and sanded smooth through 320 grit. Microscope examination (though not 100% of the surface) showed 100% penetration at the surface of the samples post sanding.
2 tests were conducted - 6 samples were tested in both ash and cherry (these were the best woods I had on hand to act as large and small pored woods). Samples were stored in the house for 30 days to ensure conditioning to ambient conditions.
Test one was with 100% water with pre and post submersion weight measurement. Upon removal of the sample from the liquid the surfaces were dried, this only took a quick swipe with a fresh blue shop paper towel. The water by and large sheeted off due to the polishing. Weight uptakes were between 4.8 and 5.1 percent with ash (I could maybe find the worksheets I recorded all this on, I'm with the process summary I wrote for myself). This was consistent enough that I did investigate any changes to the testing procedure and investigated the cherry and found a weight uptake of between 5.5 and 5.8 percent.
My personal findings were consistent enough with Ellis, 1999's paper (that test had used pine, maple and oak) that I did not question the findings.
The second test mimicked the test as performed in the Ellis paper. Alcohol based dye was mixed with water to create a penetrating solution. The test was performed in the same manner with the same cleaning post submersion. Weight gain was similar though significantly (in the statistical sense) skewed to a tighter curve that overlapped the lower end of the original curve due to alcohols evaporation and lower specific gravity (I know six samples is not great for statistical sampling but I was only willing to go so far in my house for my own process used to make my own tools)
Once weighed the samples were lightly sanded to ensure a clean surface for examination. At this point you could see the lines that the penetrate followed. in the early growth rings. Under the microscope Small specs of dye were noticeable on the end grain that were similar in nature to the speckling of acrylic on a untested sample.
The Ellis paper went into more depth in testing (upto 96h) than I was willing to do. I was simply trying to conduct enough to understand how the material would react under extreme but normal conditions (storage in a a garage in the midwest).
If I cut my samples in half you could see that the penetrate did not move significantly throughout the surface. Looking around the edges the penetrate moved further in through the early growth than through the interstitial spaces between the fibers themselves on the late growth. What I would refer to as the wood itself (the material the looked wood fiber) was untouched in the late growth. Individual fibers could be picked out at the lowish levels of magnification I had on hand (15 to 45x).
All of this assumes that whatever stabilization you're using matches the material I used. HEMA is needed to ensure near 100% penetration, blends without HEMA showed less adhesion to the cellular structure in the Ellis paper (they were able to produce SEM micrographs, much better than my little scope) and significantly more penetration into the structure of the wood itself with the dye testing.
You can find that paper here:
http://originwww.fpl.fs.fed.us/documnts/pdf1999/ellis99a.pdf