I shot in open shade in a fairly narrow alley between my apartment building and the next one over. It would have been open shade even if it was sunny, but it was also overcast.
I used a Minolta Spotmeter F, so no worries on incident metering
I don't remember the exact settings (next time I'm writing them down haha), but roughly remembered, the meter said Zone V was f/16 and 1/30, so I shot the Zone I stripe at f/45 and 1/60. After reversing the film in the darkroom to expose the other side for zone 8, it had gotten a tad darker according to the meter. IIRC the meter said something like f/14 and 1/30, so for Zone VIII I exposed at f/14 and 1/4 second.
During my initial roll film tests, I remember being surprised to find that my film speed seemed to slide around based on development time and dilution a lot more than everyone seems to say. The books make it sound like once you have a film speed, you could quadruple your development time and you'd still only gain maybe 2/3ds of a stop of density at Zone I (aside from obviously blowing your contrast out to the moon). I found that my Zone I density was affected fairly significantly by changes to my development time and especially dilution. I'm not sure if this has to do with my water (it's very hard and comes out of the tap at about pH 8.0, so the alkalinity may be speeding up development in the shadows even after the highlights are quickly exhausted or something), or some other factor.
So at this point my working hypothesis is that my film speed calibrations for roll film will be very close to correct for sheet film, but my agitation for roll film is so much more vigorous, that by comparison my sheet film agitation is practically equivalent to stand development. When I tried to increase my contrast by using Dilution B instead of Dilution H, it was like stand developing in more concentrated developer - doesn't affect the highlights a whole lot because of local exhaustion, but brings out detail twice as fast in the shadows.
My next trial will involve twice as much agitation (once through the stack every 30 seconds instead of every minute), but going back to dilution H. We'll see if the results from that next test poke holes in my theory that increasing my agitation is really the key to getting more normal results.