Traveling with Hummingbirds

hummingbird in joshua tree
Hummingbird at our window in San Francisco

Travel Essentials: A nectar feeder

 I like to get a good look at the birds wherever I’m staying. It’s easy enough to throw out some seed or set out some fruit and see who comes to call. Also easy to stick a hummingbird feeder in your luggage. They zip from flower to flower and are hard to see. Set out a feeder full of sugar water, and they’ll find it within a day and start hanging out being photogenic. Especially in the desert, other birds enjoy the sugar. Or the water. Or the combo. Or the chance to have their photo taken.

Maybe this is excessive? Nah….. Excessive will be when I try to smuggle my feeder and a bunch of sugar water on a backpacking trip.

No hummingbirds in Africa or Australia, so next trip down under, I’ll bring a feeder and see if sunbirds or others are intrigued.

x million rats and mice are used in US labs every year —- so . . . . ?

published my estimate of over 110 million mice annually in US labs and got some criticism of my methods and the resulting estimate. Fair enough. So let’s suppose there are “only” some 30 or 50 million per year. What should we do with that info? 

Two opposite conclusions from seeing these large numbers:

This is too many animals to leave out of the federal protections of the US Animal Welfare Act (AWA)

This is too many animals for the USDA ever to be able to extend AWA protections to

As I said in my article, the truly large number of mice in labs should make us ask whether they should become “animals” in the US Animal Welfare Act. I say Yes; others say No.

Knowing my concern that Congress has said that mice are not “animals” in the eyes of the Animal Welfare Act, told David Grimm two more-or-less opposite reasons for keeping things as they are:

  1. Speaking of Research “disagrees with the idea that the animals are at risk of being mistreated because they are not covered by the AWA… that all labs that receive federal funding must answer to institutional animal care and use committees, which follow the three Rs and oversee the welfare of all lab animals. Those that don’t receive federal funds typically submit to AAALAC inspections,… It is unlikely that there are large number of facilities that are uncovered by any regulation.”
  • Except, according to the National Association for Biomedical Research, it would do something. Maybe that something would not improve these animals’ welfare, but the government would not “have the time or money to track so many animals, and that doing so would drain vital resources. Now is not the time to be seeking additional restrictions on biomedical research or endeavoring to make it more difficult and more expensive.” 
  1. To the first point, I agree (anecdotal experience and informal communication) that accreditation site visits are really quite rigorous and helpful. I don’t see that accreditation alone, without AWA inspections, is sufficient (see below).  As for their claim that it is unlikely that there are large number of facilities that are uncovered by any regulation — first, nobody knows how many [ SoR estimates 10 – 25 million, which is highly implausible, so I’m not sure I buy their other estimates]. Second, perhaps we should worry that there are labs with no regulatory oversight and that are not accredited [I certainly know of several] and why should we be confident in the quality of their animal care?
  1. On the second point, I agree that the USDA’s resources would be stretched if they upped their game to covering the other 99% of mammals in labs. From the point of view of the inspected, again, I’m not convinced. Places that have NIH regulations to follow and/or are already accredited are already doing committee reviews and annual reports, which is what AWA coverage would require. Places that aren’t, should be, and AWA coverage would make that happen.   

So, are current welfare protections good enough for mice?

I say “no,” for four main reasons:

  • There is close to zero public transparency about mouse use
  • There are many labs (No One Knows how many, because only the AWA that excludes them requires publicly reporting animal numbers) that are not accredited and are not under jurisdiction of NIH animal welfare laws and 
  • It is impossible to monitor trends in animal use, including in painful experiments, without sound publicly-available statistics
  • There’s nothing like an unannounced USDA inspection to keep people on their toes.

What to do? 

Well, it will take an act of Congress, quite literally, for mice to become Animal Welfare Act animals. That will not happen. American politics is a bit of a mess now, eh? Still there should be a system in which these animals at least occasionally receive the kind of spot-checks from government veterinary animal welfare inspectors that hamsters get.

The NIH could certainly commit to greater transparency, for that fraction (half? fewer? more?) of lab mice under NIH jurisdiction. They could add up the numbers of animals reported to them annually and post that, as USDA does for Animal Welfare Act-covered animals. They could (with resources they don’t presently have) do more site visits and make their findings public (you can get them, but only via FOIA requests).

Meanwhile, many good people are working on ways to make laboratory life better for our most important and numerous animals, if only their efforts can trickle up to administrators who know their institution can escape scrutiny of much of their animal research.  

Clay during Covid

In early lockdown, the studio was mostly closed, so I shifted to doing more work at home. Still need access to a wheel, but spent more time working on surfaces. Lizards, dragonflies, the odd scorpion — obviously this meant I should plan on a bathroom remodel, with a Carboneware sink. Which has been and continues to be a fun project, though I could live with Candidate #6 if I had to.

A bit more on mouse numbers

Andrew Rowan has written an update on animal use in drug company research, and of course, it touches on numbers of animals, and trends in numbers used. Andrew has been following this issue for a long time, and it’s his book, Of Mice, Models and Men that made me realize that any description of lab animal use for non-lab animal users had to include some description of the kinds of animals used and the numbers used. Many things have changed since his 1984 book that can affect numbers of animals used, in different directions. It does seem (but as I say, in the US, No One Knows) that animal use in commercial safety and toxicity is decreasing. Credit Henry Spira in the late 70s for bringing rabbit eye irritancy testing of cosmetics to public attention. Replacement of animals in safety testing, and changes in regulations for safety testing, may indeed be reducing animal use in this field (Joanne Zurlo et al wrote a good overview of this, though it needs an update). In the other direction. Right around that time, scientists Mintz and Jaenisch “created” the first transgenic mouse, and technologies for genetically engineering laboratory animals have been causing a boom in mouse and zebra fish use for decades now (as far as I can tell: No One Knows as no one counts these animals in the US in a systematic way). 

So, animal use in the US is decreasing in some areas and increasing in others, as far as we know. And so, how many animals are used in US labs? Like myself and others, Andrew Rowan is trying to estimate what we can only see indirectly, with each of us looking into a dark room via a different keyhole (are there still keyholes? Need a better metaphor on that). He has been closely following Great Britain stats over a few decades (where there is a legal requirement for transparency and reporting) older US literature such as survey from the National Academies’ division (ILAR) that covers animal research. His approach makes an effort to incorporate differences in use in academia versus in industry, though he has not recently published an attempt at estimating total US animal use.

He reminded me of a 1987 report on lab animal use sponsored by the US Office of Technology Assessment (OTA). That report also tried looking through a few keyholes to estimate US animal use at the time, with this caveat: 

“There are no easily obtainable data in the United States allowing an accurate estimate of animal use for research, testing, and education that satisfies all interested parties; estimates range over a full order of magnitude, from approximately 10 million to 100 million animals. These estimates have all been prepared by different people or institutions with different data sources under different standards (e.g., different time periods or definitions). Comparison of the various estimates is difficult and, in many cases, impossible.”

BOTTOM LINE on this question at this point: we really do not know how many mice are used in US labs (and know even less how many zebra fish). I know my own estimate may be high or low, if patterns of use are significantly different in pharma versus academia are significantly different. It may well under-report mouse use at the institutions I surveyed if they base their annual estimate of mouse use on their daily inventory of occupied cages. 

The Igneous Intrusions Project: Mugs

I did a show at Ruby’s Clay Studio fun San Francisco in 2019, just before leaving pottery and the US for 6 months in Australia. The inspiration was igneous intrusions, those streaks of rock in a contrasting bed of different colored rock, like when you find a seam of quartz that seeped through a bed of dark granite.

The show included some mugs (now on my Etsy page: LarryCarbonePottery, since you were about to ask). The loopy, squiggly handles are something of a signature of mine, when they stay attached through the drying and two firings. I leave the outside mostly unglazed, so the contrasting seams of colored clay show through for that geological feeling with my morning coffee. My favorite place for camping is Joshua Tree park, for the birds and the Joshua Trees and the lizards and jackrabbits — and the Wonderland of Rocks with its igneous intrusions

Over 100 Million Mice per Year in US labs? No One Knows

No One Knows.

January 2021, I published my article estimating how many mice and rats per year we use in United States labs every year. The reality: No One Knows. For two reasons:

  1. The patchwork of US regulations and accreditations means that no one is actually reporting mouse and rat use in a publicly transparent way, given that these animals are excluded from the Animal Welfare Act definition of “animals.”
  2. No one has a consistent definition of “used.”  Every mouse that becomes a data point in a paper or a regulatory test has parents, siblings, and colony-mates who do not get that far. If you include breeders and culled animals, you find a larger number “used” than if you only count those who become data points in published papers. 

My approach relied on getting annual reports to the accreditation agency, AAALAC. They get annual reports from labs they accredit, but never release such confidential info. Some labs were willing to give me their info as reported to AAALAC. Some gave me the info via their state’s Public Records act.  For the 16 labs whose data I received, mostly well-funded universities, I then compared annual rat/mouse use to annual Animal Welfare Act “animal” use on annual reports on the USDA website.  When I put those together, I found that at those 16 large campuses whose data I got, Rats/Mice were more about 99.3% of the mammals. Extrapolating from an annual report in 2018 of over 780,000 AWA “animals,” I estimated over 110 million mice and rats, which is a good three times what others – research advocacy groups and animal advocacy groups – have been saying. 

I did this project because I’d pretty much guessed pretty much this number in my 2004 book, What Animals Want, and always figured someone would do some actual data-gathering to check on this. Almost no one did, and the one group that did used European stats to get at US numbers, and I do believe they ended up under-estimating US mice and rats in the process. So, I did it myself. 

As David Grimm found writing about my estimate in Science, there was some pushback. Some pretty vehement pushback, as these things go. 

Here’s my review of the criticisms of my paper, and some response

First, my own criticisms of my project (which I do discuss in my paper): 

  1. This is hampered by having no standard definition of “used,” even for labs that do report to NIH or to AAALAC. My guess — but remember: no one knows — if you include breeders and culled animals (including the ones at commercial breeding labs) I imagine there’s a 10-fold increase compared to just counting those animals enrolled in an experiment or euthanized for their tissues. But no one knows.
  2. Even if we had an agreed-upon definition of “used,” NIH and AAALAC have not given a uniform definition of “how many” or “average daily census.” At some places, especially if they count cagesto bill to grants, there’s no standard industry conversion factors for converting numbers of cages on a given day to numbers of mice on that day, and even less, for going from average daily number of cages to total annual numbers of animals used. I found a wide range of conversion factors in my project, but the truth is: no one knows.
  3. When there is such an imbalance (my data found a 99.3 to 0.7 difference, though I actually think my 99.3% is on the low side), any small difference in the estimated balance of mice to larger animals is magnified. So, while 99.2% seems not far off from 99.6%, there’s a large difference between 0.8% and 0.4%   So if all you can really get are counts of the small numbers of animals reported to the USDA, that 0.4, 0.8 or other really could make a big difference in your estimated totals. 
  4. The big challenge with my project: if all I can get are mouse counts from a handful of institutions, mostly from those subject to states’ sunshine laws, is that sample representative enough of all US labs in academia and industry?
  5. I also only looked at one year’s data. That may be more faith than warranted in our counting and reporting systems. 

I tried to lay out my methods in enough detail that even if I’m over (or under-estimating) the project might be reproducible enough to show trends over the years. 

Others’ critiques:

Nadia Jackson at Jackson Labs thinks my university sample would not be representative, and I’m wrong to work with that assumption. She’d rather make assumptions based on commercial info from Charles River labs, which seems to be the world’s largest supplier of lab rodents. If you make certain assumptions about what percent of their revenue is mouse and rat sales, and what the average price of the mice they sell is, and an assumption that people across the country buy about three-fourths of their mice and only breed one fourth in-house AND you assume that the numbers of unsold (breeders; culled animals) at vendors selling 15 million mice per year are negligible, the total number is only about 20 million.  I do think that’s a lot of assumptions to come up with that number, and I see no reason to think her assumptions are any more valid than mine. Because as we know, with no clear windows into mouse labs, No One Knows.

Speaking of Research does not like my look over to Europe (or up to Canada or over to Australia) for the idea that the US should transparently report on numbers of animals used. Guilty as charged, but they do also critique my estimate. They point out (correctly) that my data are skewed toward large universities, or rather the subset of those that I was able to get data from (and yes: thanks to those of you who told me your mouse numbers. I promised you anonymity, and I’m honoring that, as well as to those who refused my request). True. They point out that 7 large private companies use more USDA-covered animals (e.g., hamsters, dogs, monkeys, some pigs) than the 50 largest NIH-funded universities. They don’t say how I could get at those places’ mouse and rat numbers to let me make a nation-wide extrapolation to total mouse numbers. They may be write that my sampling is not representative enough. Maybe if someone uses my methods, they can go further down the level of funding hierarchy and see if lesser-funded universities do indeed have different mouse rat ratios. That would be great. Until then, I still think I’ve got the most reproducible method.

At the National Association for Biomedical Research and Foundation for Biomedical Research, I don’t see any dispute about my estimate, just their concerns about what people would do with my estimate, which I’ll write about separately. Their estimate is that mice and rats are 95% of lab animals (notice we’re all avoiding mentioning zebra fish, where lack of transparency or standardized counting are even greater, so No One Knows if they outnumber mice. They may). That would mean that for the year I covered, there were about 15 – 16 million mice and rats. 

Animal Research is More Strictly Regulated than Experiments on Human Children???

I followed this YouTube link, the Foundation for Biomedical Research disspelling myths about animals in laboratories:

At 0.18 in this video: “In fact, some people say they’re [ US animal welfare laws ] are more rigorous than the regulations covering experiments with people.” The printed version has “children” instead of “people,” an even wilder misstatement. It’s not the first time I’ve heard this nonsense.

What makes “some people” think this? Because the animal laws require inspecting subjects’ cages twice a year? Because scientists must consider use of pain medicines when inducing cancer or fractures or sepsis or infections or heart disease? Because a committee must assure that undergraduate students know how to properly conduct brain surgery on their subjects?

To the extent that animal subjects protections are more rigorous than human subjects protections, that might reflect the things scientists can get approval to do to animals, and that we in animal research have no equivalent of informed consent that lets people opt out of experiments.

Suppose an experiment required some sort of brain surgery to study cancer. Let’s compare animal research and human research.

A human researcher starts with patients who already have cancer and are in need of treatment. In the animal lab, the first step is to cause cancer, which may require brain surgery. Difference #1: non scientist can get permission to inject brain cancer cells into human subjects. They can’t even get permission to ask human subjects to consent to this. So, far, human subjects protections are looking more rigorous.

And if we do need brain surgery, for example, to try removing a tumor or injecting a drug to kill the cancer cells? Specialist MD board-certified hospital-employed brain surgeons, anesthesiologists, ICU docs and nurses will perform the procedures and aftercare. In the animal lab, those roles may be performed by students or technicians without medical or veterinary degrees. and so an animal ethics oversight committee will (or should) scrutinize their skills rather than assume they know what they’re doing. Maybe that’s a way in which animal protections are more rigorous?

After student surgeries to cause cancer in animals, the animals go back to their cages for the rest of the project. Human patients may spend some time in the ICU, then go home rather than to a cage. Animal ethics committees then will do a cage inspection twice a year, and if the animals are a species covered by the United States’ Animal Welfare Act, a government vet will see them once a year. So is oversight of how we cage our research subjects more rigorous for animals? I don’t see a human subjects committee approving a scientist to cage her human subjects, and in fact, prisoners in jails are considered vulnerable subjects hwo get extra protections.

Pain management? For the human volunteers, decisions about pain management are decisions about what is the best for this patient, balancing side effects and addiction potential against what makes a post-surgical patient experience less pain. For animals, the scientist must consider using pain medicines and must consult with a veterinarian, but can sometimes get approval not to treat the pain, if that might affect the data he’ll get from the experiment. If an animal committee pushes with more rigor to get details on pain management, it’s because pain management with animals remains optional, whereas it’s automatically the standard of care for human patients and subjects.

There are lots of compelling arguments in favor of animal research, and reasons to promote its acceptance in the public. This justification, however, rings hollow.

Analgesia for Animals: My Lottery Theory of Multimodal Pain Treatment


My Lottery Theory of Multimodal Animal Pain Management:

Good lab animal welfare requires effective treatment of any pain scientists cause. It is way too easy to pick a drug from the list, pick a dose, and never really know if the drugs is actually helping the animal feel better. One variation on this is to use three drugs, or multimodal analgesia treatment — going Beyond Buprenorphine (the most common single-agent treatment) to maximize pain relief

It’s been years now that I’ve been advocating combining different classes of pain medicines to treat research animal pain. I haven’t always prevailed; most notably, I consistently failed to get the vets or the animal committee on my recent job to enforce this standard on one particularly resistant monkey-user scientist.

I think a lot about evidence-based ethical treatment of animals when the evidence just isn’t there. When it comes to fine-tuning pain treatments for animals, our evidence is so very sparse. Whether it’s monkeys, mice, fish or others, how do we evaluate the level of pain they’re experiencing? How do we evaluate if pain medicines truly make them feel better? How then can we know if combining analgesics is even better (or worse) than using single drugs? What about side-effects of pain drugs? What about how either drugs or untreated pain might affect the experiments the animals are on?

We totally lack the most important info for even our most common drugs, and that is, what if our animal patients could self-medicate or somehow tell us they need another dose, or a stronger dose, of their pain meds?

Frankly, we don’t have the info we need to pronounce on the best pain management — other than the obvious, which is to first, cause no pain. And so IACUCs end up making an ethical decision, in what I call the ethics-of-uncertainty. Do they err on the side of caution, and require more aggressive pain treatment than some scientists want to provide? Or do they privilege concerns about how drugs will affect research data?

With my recommended 3-drug multimodal regimen, we combine an opioid (usually buprenorphine; an MD would rely more on morphine or codeine) with a Non-steroidal anti-inflammatory NSAID (for animals, we use carprofen or meloxicam; an MD might rely on ibuprofen) and also, a local “block” at the surgical incision (bupivacaine or lidocaine; your dentist uses a lot of lidocaine). Our doses for these drugs are not wild guesses, but neither are they very solid science either. We don’t know exactly how much to use, we don’t know when to re-dose, we don’t give mice or monkeys their own medicine chests, and we don’t have the best skills at round-the-clock pain evaluations.

Hence, the Lottery Theory: use all three and hope you’re getting at least one of them mostly right. While I’m watching the science develop and hoping we’ll get good answers on just what pain management, my short term approach is that we should buy three tickets in the analgesics lottery, and hope at least one of them is a winner. And yes, let’s scale back on doing painful things to animals in the first place

A new mouse painkiller in your medicine chest

This is what vets in animal laboratories need: a painkiller for mice (and other creatures) that is

— Fully effective for all strains, ages and sexes

— Completely safe with no unpleasant side effects for the mouse

Will not interfere with the experiments – for neurobiologists, no drowsiness, disruption of Learning or other effects on brain and nerve function; for cancer biologists, no effects on immune function; for immunologists, no effects on inflammation or immunity.

Long-acting, since you might get a monkey user to come in at night to re-dose the painkillers, but you will not get many mouse and rat users to do that

We do not have that, and so the search goes on.

Years ago, I did this wrong (I’ve written about that here): Meloxicam was a hot new dog-cat non-steroidal anti-inflammatory drug (NSAID), that might have advantages over Carprofen that we were current using, if only because the oral version is really tasty. Mouse doses of carprofen are about the same as for dogs and cats, so I started prescribing Meloxicam for mice at the same dose (around 0.2 to 0.3 mg/kg) that I’d use for dogs or cats. Two years and many under-treated mice later, the good vets in Newcastle did actual studies, and my mouse dose was about 3% of what would have actually helped those deserving animals.

And as we look for the magic long-acting safe effective non-interfering NSAID, we’re also hoping for an opioid that fits that bill.  Opioids are drugs like morphine, fentanyl, codeine and hydrocodone that work on different pathways than NSAIDs, and have less effect on the immune system. The best we’ve had to date is Sustained-Release Buprenorphine (SR-Bup). It’s not perfect and still in need of many more studies to best establish the right doses and dosing frequency, but it is now well-established in many laboratories. Scientists should resist quick changes in the pain medicines they use, as there can be subtle differences in experimental outcomes when they change things around.

SR-Bup has a big problem limiting its use, a regulatory rather than a biological problem. It’s classified as a compounded drug, not as an FDA-labeled medicine, which requires a vet’s prescription. By contrast, FDA-labeled drugs can be purchased by research facilities without relying on an individual vet’s narcotics license. For some vets, that’s a personal legal risk they don’t want to take, and I can see their point.

Enter Simbadol, a newer long-acting version of buprenorphine FDA-labeled for cats. It doesn’t require a vet’s narcotics license (though it is still an off-label use to use it for mice; not many drug companies are investing in the FDA labeling process to make mouse drugs).  NOTE: I have no financial stake in either version of buprenorphine, though I did publish a paper on SR-Bup’s use in mice.    

So, let’s all jump to Simbadol for our mice, shall we? I say, not so fast. Responsible veterinary care means evidence-based pain management. What we know so far is that it seems to work for cats, at a dose and dosing frequency determined in lab and in feline clinical trials. Will it work in mice, help them feel better and not worse (i.e., effective with minimal side effects)? How long can it last before it needs re-dosing? Will it change experimental outcomes compared to whatever painkillers the lab is currently using?

Well, we don’t know. I find two articles on-line (here and here), both very small studies, not independently replicated, and in rats, not mice. Neither found compelling evidence of effective pain management, and then, for only about an hour, not the 48 – 72 hour efficacy we are hoping to see. It’s possible that the assay they used (time until the rats move their foot from an obnoxiously hot light shone on the sole) is not the best approximation of surgical pain, so it’s possible the drug performs better in clinical use than in the lab. Possible, but we do not know. We know that very few drugs use the same amount and frequency in mice and cats, given their vastly different metabolic rates and possible differences in opioid processing.  

BOTTOM LINE #1: it would be poor practice to jump on Simbadol for treating mouse post-surgical pain at this point, without a lot more studies showing that it works, and for a long enough period of time

And BOTTOM LINE #2: we still need to know more about the other Buprenorphine formulation, especially as a sole agent without concurrent NSAID analgesics, and choice of painkillers is therefore much less important than finding non-surgical ways of conducting an experiment.