I've been playing around with it to see how it behaves in the macro area. I shot some small orchid flowers (Oberonia cf. lunata), total height 2 mm each, with MPE 65 mm at 1:1, 2:1, 3:1, 4:1, 5:1 and with TC 1.4xIII at 7:1. Each set at f/2.8 and f/4: all open for maximum resolution (here meant as the traditional separating two points in object), and 1 stop down for possible aberration correction and overall improved image quality. Between 60 and 175 frames were shot per set-up. Flashed manually with MT-24Ex at around 1/64-1/32 power, so very short exposure times. Flash heads mounted off lens to ensure consistent illumination angles. Stacking done on Cogynsis Stackshot with steps down to 19 µm. Stacking steps calculated as 70% of depth of field with circle of confusion = 0.03 mm in 8 x 10" print.
Processing on 6 core MacPro soup can with 32 GB RAM. Mac OS Yosemite does not reliably display thumbnails of CR2 file icons in finder. No idea why. RAW files were run through DxO (latest download). It takes time to process >100 files, but can be done on MacPro. Activity monitor had all processors going full throttle for several minutes, with quite a bit of heat coming out of the vent. I would not advise doing that on a laptop.
In previous tests with 5D2 files, RAW file processing was quicker in DxO than in PS CS5.5 extended with batch processing.
Stacking in ZereneStacker with 300 MB 16 bit .tif files was flawless. For me the P-max algorithm works best.
With the huge file sizes and small pixels (4.16 µm), the question arises at what magnification is nothing gained anymore in terms of better information? This point is reached at 4:1, where f/2.8 becomes effective f-stop f/14. This is a bit higher than what diffraction limited calculations arrive at (f/6.7–11, in most discussions). f/4 resulted in slightly softer images.
Comparing 5D2 images of same plant to the 5DsR, 5D2 still gains information at 5:1 (did not try 7:1), but still on fewer pixels. With 5DsR you can take a larger field of view at 4:1, print larger, and crop heavier, and get same information, mostly as expected.
Rik (pers. e-mail) commented that f/14 cut-off is largely in line with some other experiments posted/discussed here http://www.photomacrography.net/forum/v ... 164#101164 The extrapolated cut-off for FF 50 MP is f/17. I think the discrepancy lies in Rik shooting test-charts with B/W line pairs, while I shoot a real-world object with much lower subject/object contrast so lower starting point at MTF, and also in orange tones, so a about 10% longer wave length than standard 550 nm. 1 f-stop lower for real world in orange sounds about right.
I did shoot the same plant also at 5:1 with effective f-stop f/16.8, and I could not get any more information out of the file.
Attached is a 4:1 f/2.8 image, 111 image stack: full image height down sampled to 1000 pixels, cropped some of the black side areas out. Then second image is a 100% crop at 1000 pixels wide Again, flowers are 2 mm high, the bubbles are individual cells, about 20–40 µm in diameter, resolution limit seems to be at around 10 µm, which is about right for anything short of epi objective lenses on compound microscope. On dedicated stereomicroscope you can get down to around 4–6 µm (1.22 lamda/NA). The image is a straight output from Zerene. No cleaning, no capture sharpening, no output sharpening, just the straight stacked file.
Have to dig out the SEM image of a similar species, just for comparison. Some of the people here may get a kick out of it.

