However, my understanding of this might be completely wrong.
To clarify, the exposure scale of the process applies to the process, regardless of the negative used. But within the stipulations you also provided yourself: that in a workflow with digital negatives, you'll adjust the negative for this by digital means. In silver gelatin, you indeed expose, develop and perhaps reprocess the negative to suit the purpose. The net result is comparable however: a negative with a density range that matches the requirements of the printing process.But does it only really matter for analog negatives, or does it equally apply to digital negatives?
Does anyone know a definitive source about the topic of optimizing negatives for the hybrid-workflow?
Quite the opposite - it's entirely correct!
To clarify, the exposure scale of the process applies to the process, regardless of the negative used. But within the stipulations you also provided yourself: that in a workflow with digital negatives, you'll adjust the negative for this by digital means. In silver gelatin, you indeed expose, develop and perhaps reprocess the negative to suit the purpose. The net result is comparable however: a negative with a density range that matches the requirements of the printing process.
But I don't remember
with digital negatives, is there then any advantage of a process having a long tonal scale when, in theory, we can bring all tones in line through linearisation?
I wonder if we're running into physical limitations of a printer's 'resolution' in term of ink density...
Coincidentally, I did some mucking about with New Cyanotype some time ago and bumped into this issue as well: https://www.photrio.com/forum/threa...surprisingly-short-curve-high-contrast.206252
The TL;DR is that using a strong acid (HCl) expanded the ES (in your wording) of the process.
my multi-colour cyanotype work
If you have access to Hahnemühle Platinum Rag
Your question is the opposite of what @maverickaesthetics is asking. Maybe it's better to make a separate thread for it.
This thread is about how to produce negatives to fit the requirements of an analog, 'alternative' printing process.
Your question is about how to make silver-gelatin negatives optimally suited for digitizing with a camera. That's a different issue.
That's exactly the reason why I'm using sulfamic acid ;-)I frequently use HCl also for other purposes and never found it particularly wayward to work with. I use the hardware store 10% concentration that's common around here. It's not particularly nasty, apart from the fact that it will make anything with a hint of iron in it rust.
I take it you do the madder-toned layer first?
While I've been printing with various alternative processes for a number of years and have read many books, reading through my just received copy of Don Nelson's (fantastic) book on Kallitype, VDB and Argyrotype brought up a question that I hadn't previously considered.
The book is very well illustrated and contains a lot of comparisons regarding paper and toners and how they play with the different processes. One of the attributes that's always listed, is exposure scale (ES) for both, toners as well as papers.
Since I often print kallitypes (which I develop with sodium citrate), I looked closely at the table listing dmax and ES for the different toners. I'm mostly printing on Hahnemühle Platinum Rag (HPR). In Don's book, the dmax on HPR for kallitypes developed with sodium citrate is 1.42 and (for example) borax is a much lower 1.33. However, the ES behaves the exact opposite: 1.9 for sodium citrate and 2.7 for borax. That initially confused me.
From my (admittedly limited) understanding, ES is defined as how many steps a given process can reproduce on (for example) a Stouffer stepwedge between paper white and pure dmax. So, in essence, it is a measure of contrast - high ES representing a low contrast and low ES representing a very contrasty print.
Here comes my question: with analog negatives, ES seems a very important piece of information for the process, since the negative has to be exposed and developed to cater to the limitations of the process. But with digital negatives, is ES really an important factor? If we do a proper linearisation, we do compensate for the shortcomings of the process, don't we? If we have a process with a long ES (say, salt printing), then we print a negative with very dense highlights and the curve takes care of the rest, making sure the tones between dmax an paper white land in the right spot. Now, I can see that it might be easier to linearise for a process with a long ES (if you can print a dense enough negative) since the density variations on the negative between tones are greater, but in theory, it should be possible to linearise both perfectly: processes with small and large ES. And only dmax really counts to expand the 'scale' of a print.
However, my understanding of this might be completely wrong. If so, please forgive my ignorance. I would like to hear some insights into this from people way more experienced than me. In the past, I've just glossed over the mentioning of ES, but re-reading some of the books in my bookshelf (and Christina Anderson's fantastic new paper chart on alternativephotography.com), the term seems to be omnipresent. But does it only really matter for analog negatives, or does it equally apply to digital negatives?
Thanks for any insights,
Jo
One thing I have learned is that we adjust the process to match the negatives these days rather than the other way around, so we have figured out our
process times , methods that work well with each coating we are trying to develop.
This will mean we use the same negative for all process, silver, gum, cyanotype and pt pd. We calibrate using Palladium prints the step wedge
and this the only profile we use to make our digital negatives.
Ok I see your point, maybe I can suggest that with gum all bets are off, it is not a photographic process but rather a gum hardening process. I use a very warm water with agitation bath, I feel Calvin uses the same for his carbons, and in my space the gum process is done within three minutes maybe 4 if my first bath is not warm enough, I apply water to the back of the print and then to the front of the print within the first 20 seconds and in my world the same profile is used for gum as pt pd , cyanotype or silver.Bob, I think I read that before (or maybe gleaned it from one of your YT videos). And I think you might be one of the few to actually work like this.
Maybe I'm misunderstanding something here, but I feel that is disregarding one of the benefits of digital negatives: to cater them to your process (and not the other way round). I use the same tools you mention (QTR, Richard Boutwell's program and a spectrophotometer) and it's easy enough to create a curve (or required density) for each process. The required density for gum and pt/pd is quite different, so I'd much rather not lay down as much ink for gum if I don't have to.
The only processes I struggle to get a good calibration on are pigment processes (gum bichromate and PrintMaker's Friend in my case). And that's mostly related to me failing to be consistent enough in my coating. It's ok, but not as precise as I would like it to be. I really appreciate your experience with gum (and some of your old videos were one of my inspirations to get into the process). How did you adjust your gum processes to use the dense pt/pd negatives? Through contrast control via proportion of bichromate? Also, any tips on consistent coating would be greatly appreciated ;-)
As a side-note: Bob, I have the second print from above (the one with the door) as a gum bichromate version in the same gum exhibition as you next week. I never thought this possible even a few months ago...
Bob, I think I read that before (or maybe gleaned it from one of your YT videos). And I think you might be one of the few to actually work like this.
Maybe I'm misunderstanding something here, but I feel that is disregarding one of the benefits of digital negatives: to cater them to your process (and not the other way round). I use the same tools you mention (QTR, Richard Boutwell's program and a spectrophotometer) and it's easy enough to create a curve (or required density) for each process. The required density for gum and pt/pd is quite different, so I'd much rather not lay down as much ink for gum if I don't have to.
The only processes I struggle to get a good calibration on are pigment processes (gum bichromate and PrintMaker's Friend in my case). And that's mostly related to me failing to be consistent enough in my coating. It's ok, but not as precise as I would like it to be. I really appreciate your experience with gum (and some of your old videos were one of my inspirations to get into the process). How did you adjust your gum processes to use the dense pt/pd negatives? Through contrast control via proportion of bichromate? Also, any tips on consistent coating would be greatly appreciated ;-)
As a side-note: Bob, I have the second print from above (the one with the door) as a gum bichromate version in the same gum exhibition as you next week. I never thought this possible even a few months ago...
Actually, this is quite right. And I like your idea of specifically creating a targeted black layer. But looking at Calvin's prints, for example, and knowing that he prints 'proper' CMYK prints, I wonder if it just has to do with the profile to create the separations. I can't imagine that if you do a specific colour profile for a process, that the k layer is indeed useless. I think you are correct if you're using one of the standard CMYK profiles (that were created for the commercial printing industry and take into consideration limits of the printing processes that industry uses), but if you have a profile for your process, that should produce a meaningful black channel.The K is the layer or negative that if most people understood what its actual purpose was would not be using it.
But looking at Calvin's prints, for example, and knowing that he prints 'proper' CMYK prints, I wonder if it just has to do with the profile to create the separations.
I have read Calvin's gum printing manual and the calibration one. And I've been on his two-week colour Printmakers Friend workshop a year ago.Have you read his Gum Printing manual?
The definition of UCR - under colour removal and GCR - grey component removal is beyond my scope to explain here
And I too apologize if I have taken the thread off topic,, OOPss
He's got a very scientific approach (I work in science, so this isn't too strange for me)
It's a fundamentally different approach, one is created BEFORE printing, one is created DURING printing. But the result can be the same.
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