Administrator Pruitt initiates overdue changes to bring transparency, integrity to rulemaking
Guest opinion by Paul Driessen
Environmental Protection Agency Administrator Scott Pruitt has proposed to end the longstanding EPA practice of using secretive, often questionable, even deceptive science to support agency policy and regulatory initiatives. His proposed rules will ensure that any science underlying agency actions is transparent and publicly available for independent experts to examine and validate – or point out its flaws.
It also responds to growing concerns that extensive scientific research in environmental, medical and other arenas cannot be replicated by other scientists, or is compromised by cherry-picked data, poor research design, sloppy analysis or biased researchers. The situation has led to calls for increased sharing of data and methodologies, more independent peer review and other actions to weed out problems. There is no excuse for hiding data when studies are funded by taxpayers or used to justify regulations.
The situation has been especially acute at EPA. As Mr. Pruitt observed, “The ability to test, authenticate and reproduce scientific findings is vital for the integrity of the rule making process. Americans deserve to assess the legitimacy of the science underpinning EPA decisions that may impact their lives.”
That is particularly true for regulations that exact millions or billions in compliance costs, affect thousands of jobs, target industries and coal-fired electricity generators that regulators want to close down, or seek to replace all fossil fuel use with “renewable” energy. With the cumulative economic impact of federal regulations reaching nearly $2 trillion per year, research reform is absolutely essential.
We need regulation and pollution control – but it must be based on solid, replicable, honest science.
Congressman Lamar Smith (R-TX) has held hearings and championed multiple bills to address the problem. Several have been passed by the House of Representatives, only to languish in the Senate. With courts offering little or no help, Executive Branch action may be the only remaining solution.
Deceptive, faulty science on fine particulate pollution (PM2.5) was the bedrock of the Obama EPA’s war on coal. Particulates don’t just make you sick; they are directly related “to dying sooner than you should,” EPA Administrator Lisa Jackson falsely told Congress. There is no level “at which premature mortality effects do not occur,” Mr. Obama’s next Administrator Gina McCarthy dishonestly testified.
At the same time they made these claims, they were presiding over illegal experiments on humans – including people with asthma, diabetes and heart disease – who were subjected to eight, 30 or even 60 times more particulates per volume, for up to two hours, than what EPA claimed are dangerous or lethal. None of them got sick, proving that EPA’s claims were false. The agency refused to correct its claims.
EPA took a similar stance on mercury – asserting that power plant emissions were causing dangerously high mercury levels in American children and pregnant women. In reality, US power plants account for just 0.5% of all the mercury in the air Americans breathe, and blood mercury counts for US women and children are well below even EPA’s excessively safe levels, according to the Centers for Disease Control.
How did EPA’s junk science, illegal experiments and heavy-handed regulations pass muster? For one thing, politics too often dictated the science. In addition, the agency paid more than $180 million over a 16-year period to institutions represented by members of its Clean Air Scientific Advisory Committee (CASAC), which often rubberstamped studies and conclusions that failed integrity and transparency tests.
On global warming, EPA issued an Endangerment Finding, which claimed emissions of (plant-fertilizing) carbon dioxide from burning fossil fuels threatened the health and welfare of American citizens.
It reached this conclusion by looking only at studies and computer models from the Intergovernmental Panel on Climate Change, while ignoring volumes of studies by independent scientists who found no such threat. EPA officials even told one of the agency’s own senior experts that his studies would not be shared with agency staff and he was to cease any further work on climate change, because his analyses “do not help the legal or policy case for this decision” that fossil fuel CO2 emissions endanger Americans.
EPA was also a principal force behind the “social cost of carbon” scheme that supposedly calculated how much CO2-driven climate change would cost the United States and how those costs would be reduced by slashing fossil fuel use. The alleged cost of damages began at an arbitrary $22 per ton of carbon dioxide released in 2010, then climbed to an equally random $30 per ton in 2013 and $40 per ton in 2016.
Incredibly, EPA modelers also claimed they can accurately forecast global temperatures, climate and weather, technological advances, economic development, living standards – and damages to global civilizations and ecosystems from US carbon dioxide emissions – for the next 300 years! Moreover, in the real world, the benefits of using carbon-based fuels and improving crop, forest and grassland growth via higher atmospheric CO2 levels outweigh hypothesized costs by at least 50-to-1 to as much as 500-to-1.
Deceptive, politicized, policy-driven “science” like this pervaded EPA regulatory actions for too many years. Reaction to Mr. Pruitt’s corrective actions show how poorly informed his critics can be.
- The changes will force researchers to reveal personal or confidential information about participants in health studies. No they won’t. Such information is not needed and can easily be redacted.
- EPA can keep us safe from harmful chemicals only if it takes full advantage of all available scientific research. Public health and safety depend on ensuring that research and data purportedly supporting it are made public and carefully reviewed by multiple experts, to ensure accuracy and integrity. EPA will take full advantage of all available research that passes these tests. Tax-funded studies should all be public!
- The rules will exclude studies that rely on outside funding sources which limit access to underlying data. Those studies should be excluded. The funders need to revise their policies to ensure integrity.
- The rules will exclude so much research that they will endanger public health. Not so. The only studies EPA will likely not see is what researchers know will not pass muster, and thus do not submit. The real danger comes from research that is based on shoddy data, algorithms, models and analyses that past researchers have been able to keep secret. That is precisely what the rules will ferret out and correct.
- Pruitt has removed scientists who receive EPA funding from participating in advisory committees. As noted above, those scientists had received millions of dollars in exchange for supporting EPA analyses, initiatives and regulations. Pruitt wants input from experts whose views can be trusted.
- Pruitt has criticized the peer review process. Too many peer reviews have been conducted by closed circles of associated scientists who rely on government grants and support regulatory decisions to maintain funding. Some refused to share data with experts who might critique their work – or worked to keep contrarian research out of scientific journals. The fact that some journals rarely require access to or review of underlying data further demonstrates why the peer review process also needs to be reformed.
Too many past EPA policies, policy-driven research and regulations have been employed to force the nation to abandon fossil fuels that still supply 80% of US and global energy – and switch to expensive, intermittent, unreliable wind and solar energy installations that will require unsustainable amounts of land and raw materials, while destroying wildlife habitats and slaughtering birds and bats by the millions.
Those actions also killed numerous jobs and left many communities impoverished. Simply put, the danger to Americans’ health and welfare, livelihoods and living standards is regulations imposed in response to secretive, sloppy, substandard science that has ill-served EPA and the nation.
Ethics charges against Mr. Pruitt should be evaluated with all this in mind – and while acknowledging that members of Congress who are railing against him never complained about Lisa Jackson or Gina McCarthy’s CASAC payment abuses, illegal experiments on human test subjects, false testimony about particulates, EPA-orchestrated sue-and-settle lawsuits that imposed billions in regulations while enriching environmentalist groups … and junk-science regulations that cost the United States incalculable billions of dollars, brought no environmental benefits, and impaired the welfare of millions of people.
Pruitt’s reforms are long overdue. Honest politicians, journalists and voters will applaud him and them. Other government agencies should initiate similar science and rulemaking reforms.
Paul Driessen is senior policy analyst for the Committee For A Constructive Tomorrow (www.CFACT.org) and author of books and articles on energy and environmental policy.
The AAAS has this statement of Policy and Public Advocacy on its Website;
So should we take Dr. Rush Holt’s word on this?
Let’s be skeptical and break it down and analyze.
His first point is on secret science is with a reference to epidemiological studies and patient information.
– With first-hand knowledge, I can tell you (the WUWT reader) that every study since the late 1990;s has had an Institutional Review Board (IRB) in the US and Canada approval process. The IRB views patient confidentiality and patient consent to participate in any clinical or clinical research proposal study of highest concern. They (the school, hospital, clicnic and investigators) can get their butts sued-off by a trainload of money-hungry tort-bar lawyers representing aggrieved patients if they violate it, along with possibly losing NIH funding.
The IRB at every medical school and their associated hospitals and clinical study participating hospitals, VA hospitals doing research studies. and military hospitals are under NIH scrutiny (and possibly CDC and/or FDA) where confidential patient records are of course kept by attending MDs and medical-licensed clinical staff. All clinicians and staff are subject to the Health Insurance Portability and Accountability Act of 1996 (HIPAA, US only) confidentiality. The approval for these studies by the IRB mandate protection of patient confidentially when data is removed from patient records and pooled, analyzed, and subsequently published to inform the entire medical community of important results.
As such, any clinical study in the US now must have a NIH-issued study number, confirming compliance with approved IRB and NIH guidelines in all areas of patient confidentiality and possibly Good Laboratory Procedures (GLP) where required. No credible peer-reviewed journal editor will accept a clinical or human study subkject research related manuscript without Methods section of that manuscript clearly stating IRB and NIH compliance was adhered to where patient-clinical study data are used.
So for PIs and named investigators (in the IRB proposal all proposed studies must submit), all PIs and investigators are named, by-name, and protocols are inplace to mask patient identifying data to use this information in which they want to publish or move it outside cliniical hands and data systems. For over 20 years now, there are extraordinary efforts and expenditures in place (hiring specialists trained in HIPAA and data handling) that Principle Investigators (PIs) and all associated investigators must utilize to mask identifying patient information in the data analyses before that data leaves licensed HIPAA-trained clinician hands and their patient records. This masking and stripping out of patient-identifying data is now quite routine and already demanded by the IRBs for approval of any and all human-related and clinical patient studies since 1996
No bureaucrats at EPA or any other government bureaucracy, in consideration of a proposed public rule should ever have confidential patient information, secret or not. If they do, someone has broken HIPAA and/or violated their IRB protocol and NIH directions. Both are subject to severe penalties.
Dr Holt’s next assertion in the AAAS statement is: “Other studies rely on public and private-sector funding sources that may limit access to underlying data.”
This is an extremely vague statement with no example other than possibly referring to government-funded special panels of scientists, do agency directed studies who only report to the agency. Again, they cannot use clinical data if it is not masked, and if they are doing work for the government, it should by accessible, independently reproducible, and subject to FOIA. This is acutely true when private funding for public policy studies is used in policy and rule-making (individual or corporate) where property and constitutional guarantees of being secure in homes property and liberties may be at stake in the proposed rule. And most vitally, anything less than total data transparency in private-funded studies is most assuredly open to junk science findings that serves a particular political agenda.
Dr Holt’s next statement is : “The administrator’s latest attempt to reject valid scientific evidence fundamentally mis-characterizes the way science is conducted and made available for decision-making.”
What science has Director Pruitt rejected? None is named. This is an ambiguous assertion with no facts or data. To be sure: Science is independently verifiable. And claimed science that is not independently verifiable is not science. Dr Holt most surely knows this.
Dr Holt’s next statement is: “If put into practice, EPA could prohibit, or make it incredibly costly, for the agency to use a wide swath of high-quality scientific research. ”
Federal courts have ruled that Federal agencies must consider the public costs their rules may impose. As such, the claim that it may be too costly for the agency to use high-quality scientific research flies in the face of the considerations already discussed above, namely the already quite expensive HIPAA law and compliance actions therein already in-place, and that has nothing to do with EPA or other agency rule making including the Fish and Wildlife Service, the Food and Drug Administration. The high costs are already there if the data is to be used at all (unless you are the EPA’s privately hired with public money-version of Dr. Josef Mengele).
So in consideration of this analysis (above), it is my opinion that Dr. Rush Holt’s and the American Academy for Advancement of Science’s contention that patient confidentiality might be compromised or would make unavailable such study’s conclusions to the EPA as both specious and wholly invalid.
Joel O’Bryan, PhD
[Comment found and rescued. -mod]
Joel: For a generation or three, good-gov’t types called for transparency in gov’t and passed laws requiring same. (As an aside, another post has comments that we need to pass another law requiring this, seems passing laws doesn’t necessarily solve the problem if someone is willing to set up false email accounts or, what the hell, set up her own server). Dr. Holt thinks transparency is good for others, but sometimes private funding requires keeping secrets. I’d like to know if he would extend that to, say, tobacco companies.
Mods: hate it when the SPAM or other WUWT/WordPress filters take my long posts and don’t even tell me if they are awaiting moderation. So check the Spam or other folder please.
[Yes…WP likes to sequester random posts as spam or trash. We believe it’s due to a desire to give us mods busy work. You know, to make sure we earn our salaries… -mod]
“…studies and computer models from the Intergovernmental Panel on Climate Change”
IPCC does not originate any of these studies and models of course. It’s a deceptive sentence. The main problem being that “volumes of studies by independent scientists” somehow fail to make it to the various strict peer review processes surrounding the A and B level journals. Or do not even bother.
For EPA to somehow start controlling or “fixing” the national and international scientific “communities”, not matter how fundamentally flawed they might be, would be a bad, very bad thing in principle. They are just not Keepers of the True Scientific Faith. It’s uncertain who is, but it’s not EPA.
More transparency and opening up to the debate between scientists, even when still marginal, is a good thing. But fighting fire with fire, as in this case: fighting the politicization of science by politicizing or even policing science inside the agency will simply not work on the longer term at all. A temporary Pyrrhic victory at best.
Well said sir.
Lucky USA, I wish someone like that would put a broom through BOM, marine mcience, science organisations in general, and public funded media. Then investigate and expose the funding sources of Australuan Greens party, and greenie NGOs.
We have a Royal Commision into big Banks and FIRE sector right now, wr were told it would find nothing much, the Govt were completely against it but thd public would not take no for an answer. Well guess what? The banks and FIRE sector were using political protection and media PR spinning (via former State Premier politicians spokes people) to hide there now exposed criminal activities.
The same thing has occured in all public science and public media, and it badly needs to be cleaned up, too.
End not only secret science, but also about half the regulations and employees. That swamp is a source of disease & needs draining….
This particular topic has really been a burr under my saddle for a long time. I work for one of the other Federal agencies as a scientist and we play by the rules. What I mean is that any data or decisions that are made based on said data is made available to the public. The taxpayer paid for it and it ultimately belongs to them. The idea that you can regulate and dictate policy to the proles from your ivory tower is not how we do business in this country. Or at least it shouldn’t be.
I co-host a podcast with two other guys that deals with science and history that I think the readers of this blog would enjoy. On our next episode I address this very topic in a short rant. So, if you don’t mind the shameless plug, the show is called the Seven Ages Audio Journal. It’s on all the usual platforms and the website is http://www.sevenages.org
Thanks!
I think the equitoxicity ruling, which says that all PM2.5 particles are equally toxic “because we do not know that they are not” is in danger of being revoked. It was never true and everyone knew it then and knows it now. It serves as the basis for numerous regulations and WHO targets that exist without considering what particles are made of, only their aerodynamic diameter.
The knock-on effect of revocation will be huge. Those claims for ‘premature deaths’ attributed (by committee) to estimates of PM2.5 exposure by estimates of numbers of people causing estimates of inhalation inducing estimates of disease are all based on the assumption that all particles are equally toxic: sand, dandruff, soil, asbestos, cement – everything.
If not the house of cards, at least some rooms of cars are about to fall.
In bio-medical research it is quite common to see a paper where they purportedly investigate the effect of a drug/compound, but do it very badly. Not observing any significant effect at lower concentrations, they just keep on raising the dose until a sufficient number of cells/animals die or show some other response which allows them to claim an effect, frequently with the aid of shoddy statistics and supine reviewers.
Of course one can easily do the same thing using just pure water, or glucose, or vitamin C. It is simply dreadful science and is usually recognised as such, albeit not usually in a public fashion that would embarrass the authors or cause a stink. But these sort of studies seem almost the norm in cited enviro-circles where they have a compound to ban, or an industry to destroy. If the FDA was charged with interpreting the academic output of the enviro-scare industry then we would have fewer ridiculous laws like those arising from the EPA endangerment finding.