Smut Clyde is a natural force I insidiously chose to harvest and unleash upon the worst cheaters of the research community. His previous contribution to my site, about the nanotechnology Photoshoppers Prashant Sharma and Rashmi Madhuri, flushed several promising academic careers down the toilet, quite deservingly so. Both are under institutional investigation and public ridicule, the list of their retractions grows steadily (presently at 15 retracted papers), with no end in sight (Sharma and Madhuri however try to compensate their losses by publishing new papers in Elsevier, e.g. here & here). Indian scientists even set up a Change petition, asking the Indian Government to deal with the research fraud at the Indian School of Mines (ISM) in Dhanbad.
A former partner of Sharma from Allahabad, Ashutosh Tiwari was exposed by readers of that Smut Clyde article, which awarded that fake professor from Sweden with his own string of my reporting. Tiwari saw his predatory conference and publishing business going down the drain, while the Sharma and Madhuri papers he edited and co-authored for a special Elsevier series were retracted.
Towards Chemistry World “Sharma declined to comment beyond observing that he’s ‘just a co-author on some of those papers’“.
Madhuri, before she went silent, declared to an Indian journalist:
“We would like to mention that all our articles are published in very reputed journals, after a very rigorous and transparent review process, adopted by the concerned journals. The referees and editorial board have approved our work and published them.
“Merely by inspecting the images one cannot draw inferences that are outcome of very carefully designed and performed experiments. Therefore, it is very unscientific to comment that the images are morphed or photo-shopped, whereas all the related data and supporting files are still in possession of authors, which can be crosschecked by competent authorities, if required.”
Now, Smut Clyde presents the Prequel to that story, namely the tale of Madhuri’s PhD advisor, Bhim Bali Prasad, professor in the department of chemistry in Banaras Hindu University in India. He is the senior who apparently still make up his data in the traditional artisan way: by pencil. We shall now learn where Madhuri learned her skills. Grab popcorn, and enjoy the show!
Attack of the Photoclones- The Prequel, by Smut Clyde
Two researchers at the Indian Institute of Technology / Indian School of Mines have been in the news lately for nanotechnology retractions, as reported here and here by Prasad Ravinranath. We also refer you to Andy Extance (another science journalist with an interest in research integrity who covered the Sharma / Madhuri imbroglio for Chemistry World) in return for him crediting “anonymous @PubPeer commenters and bloggers like @SmutClyde and @schneiderleonid”.
Much of the critical activity occurred at the invaluable PubPeer archive*. The full number of papers under scrutiny is not immediately obvious, due to a limitation of the site’s search function. Perhaps it never occurred to its designers that a single author could publish more than 40 papers that would later fall under the shadow of “Post-publication peer review”. Alternatively, they were worried that researchers would compete to hold the record for the number of contentious publications. Either way, the search function maxes out and only lists the first 40 hits that match an author’s or authors’ names… it is an unacceptable restriction and I demand my money back.
Anyway, Drs Sharma and Madhuri felt unfairly singled out by all the attention from image-integrity vigilantes and self-appointed blackboard monitors; they did not welcome the evidence that people were reading their papers. Allegations of extortion ensued, and threats of law-suits, and complaints to the Cyber Police.
As proof of the unfairness, Madhuri and Sharma have adduced a number of arguments, for instance citing the number of Ph.D students they have mentored (their collaborators and co-authors on the papers now under scrutiny). Indeed, this is is a useful reminder that in science we were all students once, [pompous voice] just links in the inter-generational chain of cultural transmission, custodians of skills and values that we learn and pass on [end pompous voice]. Sometimes the transmission goes the opposite way and the guru can learn from the śiṣya.
Prasad et al. (2009)
But that is not the full story, for those post-publication reviews look back over quite a number of years – ‘cold-case curiosity’ sounds better than ‘antiquarian obsession’ – and the entries for Sharma and Madhuri cover the whole of their careers, back to before they moved to Dhanbad and the Institute of Mines, to when they were the Ph.D students of (respectively) Professors Avinash C. Pandey at University of Allahabad (with his own impressive PubPeer record), and Bhim Bali Prasad at Benares Hindu University. Which brings us, in an indirect and circuitous way, to a different (though overlapping) oeuvre of academic productivity… thereby absolving our host of any suspicion of singling-out, or injustice. So this post is a prequel, as it were, to ‘Sharma’s Bad Karma’. I am advised that prequels are popular with the young people.
Prasad & Pathak (2017)
The post can only ‘scratch the surface of the iceberg’, for Prof. B. B. Prasad co-authored 68 journal publications in the decade 2008-2017 (and a couple of book chapters), peaking in 2013 with 15 papers. The general theme is a kind of lock-and-key “molecular imprinting” paradigm, promising the easy, economical and selective detection of some specific chemical of oncological, pharmaceutical, forensic or environmental interest (e.g. “an anticancerous ifosfamide drug“, or hemoglobin, or “organochlorine pesticides“). A stream of dramatic announcements and breakthroughs has ensued, though one looks in vain for developments -outside the lab, or indeed for replications.
The detector is prepared by coating its surface with what may be a precision polymer, or carbon nanotubes, or quantum dots, or any other combination of nanotech Worship Words. Crucially, the targetted molecule is one of the ingredients during synthesis of the coating, so that the other ingredients wrap around it and form chemical bonds; then the target is washed or stripped away, leaving “negative mold” cavities in the coating, complete with unfulfilled bonds… ensuring that if any target molecules appear in the environs, they will gravitate straight for those cavities and snap back into place with an audible ‘click’, measurably altering the detector’s electrical or physical properties. In many of these publications, the detectors are dual-function (“simultaneous electrochemical determination of norepinephrine and uric acid“, or “simultaneous analysis of cerium and gadolinium ions“, or “simultaneous analysis of glyphosate and glufosinate“), in the manner of novelty kitchen appliances.
So Prasad’s papers are often illustrated with side-views of electrodes, to highlight their magic coatings. This side-view shows either a “OMNiDID/PGE showing film thickness” (according to Fig 1(C) of Prasad et al., 2017), or “MIP- AuNPs films at PGE surfaces” (according to Fig 2(E) of Prasad, Jaiwal & Singh, 2017).
This imposing wall is the edge of either a “MIP-composite modified sandpaper electrode” (Fig. 3C(a) of Prasad & Singh, 2015), or a “C60 monoadduct-MIP” (Fig. 5(D) of Prasad, Kumar & Singh, 2016). We encourage recycling.
Despite variations in the scale bar, “Fig. 3. SEM images of … (D) side image of MIP-adduct modified SPCEs” in Kumar & Prasad (2012) is recognisable as “Fig. 2. … side view of coated layer over PGE, electrode 1 (F)” in Prasad et al. (2013). With a different substrate, it became “Fig. 2. … (F) side view of coated layer over PGE” in Prasad et al. (2013b).
The background void at the left appears for a fourth time in Prasad, Prasad & Tiwari (2013), as “Fig. 1. SEM images: … (E) side view of MIP modified MWCNTs–COOH/PGE”, with a substrate that was sourced from elsewhere.
“Fig. 1. …SEM images:… (F) sideview of MIP-modified GNPs-PGE” from Prasad, Jauhari & Tiwari (2014) takes its substrate from Fig. 1, “SEM images of (A) bare … CIP-modified PGE,” of Prasad et al. (2011).
A “MIP-T4 adduct modified Ag electrode for thickness measurement” (Fig 3(e) of Prasad et al. 2010) became a “MIP-AA adduct modified GE (side imaging)” (Fig 2(c) of Prasad et al. 2011). In the course of the transformation, the image lost quality but acquired a grey overlay, while the tastefully cloned ‘substrate’ at its right was replaced with ugly wallpaper.
I am not convinced that this “side view of sol–gel–DIIP/PGE” (Fig. 1D from Prasad, Jauhari & Verma, 2014) ever existed outside a Photoshop window…
… or this “side view of MWCNTs/MIP”-Carbon Ceramic Electrode (from Fig. 2(E), Prasad, Jauhari & Tiwari, 2013).
Going back to the molecular-imprinting paradigm: it has an intuitive appeal, though like all the best cargo cults, it is best to avoid inquiring too deeply into the working details. It appeals enough to keep the research grants flowing. Conceivably some actual experiments were conducted, hidden behind the photoshops, and the impostures, and the photocopied hand-drawn spectra and voltagrammetric ziggurats, and the forged time-stamps, and the shifting identifications of electron microscopy.
The photoshop component of this decade-long body of work is variable in quality. It may be that the co-authors / students are expected to contribute a composite image as a kind of journeyman’s piece, to demonstrate their mastery of the image-manipulation software that seems to be central to the BHU Analytical Chemistry curriculum. Then of course they take those hard-earned skills (and their training in the values of science) when they graduate and move on to academia elsewhere.
So here is Figure 3(B), a scanning-electron-microphotograph of “anodised silver”, from Prasad and Kumar (2014):
I like the idea that “some of the holes are very small Sasquatch prints, and the round ones were left by a hunter’s shotgun”. From the same paper, 3(A), “bare silver surface”. The patchwork assembly of repeated motifs all seems very labour-intensive and it might have been easier to find a piece of bare silver to put in the SEM.
Sometimes the repetition is so dominant, one could be reading a wallpaper catalog, not Material Science & Engineering. “Was the quintuplicated baboon’s face in (c), as marked up with red in Hoya’s depiction, originally inspired by this example from a tattoo design web site?” wondered C. Amazonicum.
Figure 3(c) and (d), Patel et al., 2009.
“Perhaps there is a desperate EM technician trapped somewhere in the basement?”
Figure 2(A), Prasad & Pandey, 2012
Elsewhere, the original image has been so stirred around by the ‘Shop distortion tools as to elude recognition. Assuming that a non-virtual starting-point did exist, though I am open to the possibility that the source was a neural network that someone trained on the depraved perspectives of Matta’s ambiguous Surrealist spaces, and H. R. Giger’s gauzy airbrushed ‘Landscape’ series.
Figure 5, Prasad et al., 2016
Perhaps the idea was to sneak in dick pics to see if anyone would notice.
At their best, these creations become nebulous dream spaces in which foreground and background blur, or vertiginous abysses, reminiscent of Dorothea Tanning.
The fractured, repeated scene above at right, fraught with legs and jaws and multiple eyes, is a vision from an arachnophobic nightmare. It could be the last image seen by an unlucky insect… or a monochrome version of Arthur Tress’s aesthetic. Fig 3(a) at left is less of an obvious kaleidoscope, and the stuttering elements only jump out at a second glance.
We need to move on, but I cannot resist showing Fig. 3(D) – “MID nano-fiber at 75,000×” (from “A dual-template biomimetic molecularly imprinted dendrimer-based piezoelectric sensor for ultratrace analysis of organochlorine pesticides”: Prasad & Jauhari, 2015) – for I am in the thrall of the meshes of its intricate symmetry. I think it was modeled on the Veve of Ogoun.
As for Fig. 3(C) (“MID-templates adduct nano-fiber at 75,000× magnification”), it seems to have started out as 3(F) of Prasad et al. (2010) – “MIP (after template extraction)-modified Ag electrode”. But elongated, and half-obscured by exuberant use of the ‘Shop Clone Stamp.**
Figure 3(A) from Prasad et al. (2016b) is as if the loosely-stacked books on my shelves sprouted eyes and stared at me reproachfully. Or like air-dried codfish heaped up in a Norwegian farm-house.
In this case, a source for the composition can be identified, for the central portion later appeared as Figure 2(A) of Prasad et al. (2017).
This is a convenient segue leading to another part of this body of pictorial invention, in which parts of the confections are used elsewhere in different contexts. That is to say, there is no internal repetition, so it is easier to forgive the journal editors and peer-reviewers for blithely ignoring their dubious nature.
At one extreme are the simple rotations, and zooms, and unadorned re-use as representations of a different nanomaterial. There are so many cases of ‘enlargement’ as an aid to recycling, I don’t know which ones to leave out. Readers will just have to explore the PubPeer archives for themselves. This transmission-electron-microphotograph shows either TNPs, or Quantum Dots.
“Fig. 1. SEM images: … (E) MIP,” from Prasad et al. (2014), or “Fig. 2. SEM images: (A) MIP-adduct” from Prasad et al. (2017)?
SEM images of “MIP modified PGEs” (Fig 5(E) of Prasad et al., 2016), or “NIP–carbon composite fibers at 10,000 x” magnification (Fig 2(F) of Prasad et al., 2010)?
At the moment my favourite image manipulation is Figure 3 from Prasad et al. (2010), in which (A) and (B) (“TEM images of crude and MIP modified MWCNTs) are simply the zoomed-in centres of photo negatives of (E) and (D) respectively (“SEM images of MWCNTs-NIP. … MWCNTs-MIP”).***
Moving right along, the “MIP-adduct” (Fig 3(C) from Kumar & Prasad 2012) is a 90° rotation of “MIMSPE fiber: MIP (after template extraction)” (Fig. 1(B) from Prasad et al. 2014). Both also have a sense of vibrant, interrupted movement that somehow brings “Neptune’s Horses” to mind… if a fondness for late-Symbolist painting is wrong then I don’t want to be right.
A mystery lies behind the “bare pencil-graphite electrode” that appeared with a 2009 electron-microscopy time-stamp as Fig. 3(C) of Prasad et al. (2010) and as 2(A) of Prasad et al. (2010b), for the stated magnifications are vastly different (60,000 x and 8,000 x respectively). When the same image featured as Figure S3A in Prasad et al. (2011), the date-stamp had changed to 2010. Co-author Madhuri must have taken the image with her when she graduated, for a zoomed-in version appeared for a fourth time in Roy et al. (2014), re-purposed as a platinum electrode.
But these digital, virtual fabrications of results are not to everyone’s taste, and it is good to be able to say that old-school analog methods are not neglected. Figure 3 of Prasad et al. (2010) is nominally the output of an IR spectrograph, but “the wobbly palsied lines that compose these overhanging, toppling stalagmites” were more likely hand-drawn with a dried-out felt-pen, photocopied and reassembled… keeping it real, as the kids say.
With their identical, forward-bowed heads, the peaks remind me of women in a Burne-Jones procession.
If you prefer vinyl records and valve-amplifier stereros to MP3 files, you are sure to like Figure 4 of Prasad and Lakshmi (2005). It is presented as a series of voltage / current functions – “Differential pulse cathodic stripping voltammograms with MIP-modified hanging mercury drop electrode” – plotted on a X-Y chart recorder, but I believe it to be some kind of hand-drawn ziggurat construction diagram.
Similar ziggurats can be found anywhere in this series of papers, overhanging and wobbling as if the contractor had used slabs of rubber instead of stone for the building material. The artist had presumably seen the rectilinear output of an early X-Y plotter, and decided that voltammograms are supposed to look that angular, without worrying too much about the ‘rectilinear’ part.
Often photocopies of a crennelation sketch are stacked up, to show how well the voltagrammetry replicates. At left is Fig. 5(C) from Prasad, Srivastava &Tiwari (2013): “run c, multiple runs show reproducibility of the measurement”.
At right, Fig. 2 from Prasad, Srivastava & Tiwari (2013b).
The crucial point is worth emphasising again and again: Professor Prasad and his colleagues have been mixing artisanal hand-crafted designs and virtuoso displays of photorealistic image manipulation, and submitting them as multiple papers a year, for over a decade. More crucially, the editors and peer-reviewers of journals with serious-sounding names like Materials Science and Engineering C, and Journal of Colloid and Interface Science, and Journal of Chromatography A have looked at the Figures each time and thought “Yes, that’s convincing, print it!”
To be fair to the editors and reviewers, maybe there were even more papers that they didn’t accept.
* Obligatory caveat: There is no rule that commentary at PubPeer has to be negative; anyone can use the platform to praise a paper and bring it to wider attention, or for that matter, to criticise it on spurious or malicious grounds – thus the existence of a PubPeer thread for a publication is not damning in itself.
** 3(F) also manifests as a SEM image of “MIP modified QCM sensor”, in Figure 2(a) of Madhuri et al (2011).
*** 3(D) reappeared as a “NIP-MIMSPE fiber” (as Figure 1(C) of Prasad et al. 2014); and yet again as a “MIP modified PGE surface” (as Fig. 1(a) in Kumar et al. 2011).
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Crazy stuff. While the re-use of figures is flagrant, I wonder whether some of the images with internally repeating elements cannot be explained by natural phenomena. I’m not in the nano field, but in my opinion it would be no simple task to photoshop the internally duplicated features highlighted in some of these figures, for example: https://pubpeer.com/storage/image-1515442066000.png. Isn’t it at least possible that in some instances these could be genuine, arising from physical processes that occur when the materials are produced – just as impressively ordered crystals can be formed from solutions?
For the specific case you mention, we can compare it against the image appearing in another publication, showing just the centre (identified as a completely different material):
Now my guess is that the “central blow-up” (at left) was really the original image, which was extended, with partial copies of itself, to compose the larger scene (at right). There is evidence of this in the right-hand scene.
I know that the “larger scene” was published first, then the “blow-up”, so my guess requires the time-stamps on the images to be forged, but there are forged microscopy time-stamps all through this body of work.
It is a lovely bit of modern art. For the novice auteur, look at the bottom left corner of the “central blow-up” and you can see how it has been modified by pasting bits of the blue duplication into it.
If you look at the top left corner of the purple duplication you can see that the right-hand duplicate has been modified by adding streaks of white with no three-dimensional layer. But this does not show up in a quick naked-eye glance.
Another interesting comparison is in the 100nm scale of the blown-up image and the 200nm scale of the larger image.
There must be a massive global network of jokers who have been passing each other’s “nano” papers into print for decades, while spawning new generations of fakers. Not one of the Prasad cohort has had the guts to answer any of the hundreds of queries raised here, on PubPeer or elsewhere with anything but hollow threats. Let’s see how much political backing they can muster. The problem with gaming the Indian system is that the thugs at the top rotate every few years. If it’s an off cycle then they are in trouble. Of course like the Great Gupta, godfather of Indian science frauds, Prasad himself will retire with full pension and civil service perks while the young ‘uns take the heat. It’s their way.
” (Indian) Nanotechnology is BS” (Elon Musk)
I first thought that these papers where published in typical predator journals that most of us avoid, but no, they are published in journals with quite good IF and under the wings of well known publishers and societies.
Prasad et al., 2016 was published by Elsevier in the journal Carbon with an IF=6.3. Not bad for a journal publishing rubish.
Patel AK et al., 2009 is to be found in another Elsevier journal; Materials Science and Engineering (IF=4.2). Not at all bad.
Prasad BB and Kumar A, 2014 can be read in the Journals of Matherials Chemistry B published by the Royal Society of Chemistry with an IF of 4.5.
The epidemic of junk science must be stopped and here are some suggestions:
An international Research Integrity office with power should be established under UN/WHO.
An international black list of fraudulent scientists and research institutions that do not follow the rules should be distributed to publishers and research institutions.
Medline/PubMed should run quality control of all indexed journals using duplication screening and ban journals that exceed a defined limit. The number of journals indexed should be reduced considerably.
A dream for sure, but indeed necessary.
“The fractured, repeated scene above at right, fraught with legs and jaws and multiple eyes, is a vision from an arachnophobic nightmare.”
We were discussing this with the wife, and we decided that it looks like a nice dog with it’s mouth open and tongue out. Also she told me that a long time ago, before we were born, but possibly also as late as when we were elementary school students, there were IR machines at research institutes that did not have XY plotters even, and what some people did, was put a paper on the screen and trace it with a pencil. Then I suppose it would be possible to get two y values for one x, if you’re bad at tracing the screen… It seems far fetched for today (trying to avoid mentioning my age, but the fact that I’m typing this comment and I have a PhD puts some lower bounds on it), even for an out of the way Indian research institute ten years ago. And anyways, IRs are the stupidest thing to fake for a material such as this. Here the intensity of peaks at around the 500 wavenumber region seems suspiciously low if you’ve got organics of all sorts, such as indole. Surely you could just throw some stuff lying around in the lab in a KCl matrix and get all those peaks that you need and no one would care. If you were looking for an adsorbed CO peak, then it would matter more. And the newest IRs are cheap, don’t need any sample/matrix prep, and can measure in a few minutes.
The accompanying text typically specifies an “X–Y chart recorder (PAR model RE 0089)”.
Well, the x-axis with the wavenumber labels inside the figure also looks like it was very likely not done by hand, unless it was two different people doing the spectrum and the axis and the meticulous one got the axes job. 😉
I forgot to mention the “Prizes” section of B. B. Prasad’s illustrious CV:
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