White-Nose Syndrome

A Decade of White-Nose Syndrome in America: What We’ve Learned
11/29/18
By Merlin Tuttle

Mount Aeolus Cave in Vermont with floor covered in WNS-killed little brown myotis (Courtesy University of Tennessee).

The bat-killing fungus, Pseudogymnoascus destructans, that causes white-nose syndrome (WNS), has triggered the most serious wildlife disease epidemic in American history. It came as a huge surprise. Nothing similar had ever been seen. Faced with a crisis without precedent, wildlife managers could only guess at how best to proceed. The immediate goals were to halt the spread and find a cure.

Nevertheless, WNS has proven unstoppable. Bats have spread it rapidly across an entire continent since 2008, killing millions of cave-hibernating species. (1) (2) This is extremely discouraging. However, the most dire predictions have not come to pass, (3) and encouraging discoveries have been made. It’s time to review what we’ve learned.

Little brown myotis hibernating in a Michigan mine prior to the arrival of WNS.

A search of recent literature, combined with standardized interviews carried out by volunteer Ann Linder, revealed improvements in WNS policies and reasons for guarded optimism. She contacted at least one natural resource representative from each of the first nine U.S. states infected, and I followed up where further detail was needed. Our goal was to uncover insights that might improve future WNS management.

We focused primarily on the little brown myotis (Myotis lucifugus) due to insufficient observations on the other most impacted species (northern long-eared myotis, Myotis septentrionalis; tricolored bats, Parastrellus subflavus).

We were encouraged to learn that, even the little brown myotis which commonly sustained losses of 90 percent or greater, appears to have stabilized and is showing encouraging signs of recovery over broad areas, despite early fear of extinction. All six states conducting surveys reported either stable or growing populations.

_Wing from dead eastern pipestrelle (Pipistrellus subflavus) bat shows points of orange-yellow fluorescence when exposed to UV light. From Turner and others, 2014, Figure 1E, page 569.

Pennsylvania reported innovative attempts to improve hibernation roosting opportunities. Initial results from modifications designed to lower and stabilize temperatures have been encouraging. (4)

Some intriguing discrepancies were noted, particularly in Massachusetts. A regularly surveyed mine sheltering 8,000-10,000 little brown myotis pre-WNS, fell to just 8 by 2013, and still numbered only 11 by 2017. In the same state a nursery colony that averaged 500 individuals pre-WNS fell to 157 between 2009 and 2011. Nevertheless, it has grown steadily since 2012. By 2017 it recovered to 454. Harp trap samples were taken along emergence flyways, and more than 200 bats were banded. Recaptures in subsequent years have documented muli-year survival and successful reproduction, but their hibernation site remains undiscovered. (5) It is tempting to question the extent to which these bats may have benefitted from apparent use of hibernation sites unknown to humans or that provided superior hibernation conditions.

The most informative pre- versus post-WNS study we found, reported on a nursery colony that in 2008 contained approximately 1,200 little brown myotis living in a large bat house in northern New York. (1) WNS arrived in 2008. In 2009, emerging bats were sampled in mist nets and traps along flyways, banded, recorded and released. Exit counts (adults and juveniles) fell to 145 in 2010, an 88% decline. Since 2010, exit counts have increased annually, to 256 individuals in 2017. Based on initial decline rates for the species, extirpation was anticipated, and the outcome remained unclear for three years. It has taken 10 years of post-WNS monitoring to document stabilization and recovery.

Nursery colony of little brown myotis photographed by Caroline Van Kirk Bissell in bat house mounted on a garage in southwestern New York prior to arrival of WNS.

I personally discovered an apparently similar occurrence in southwestern New York. Several bat houses, mounted on a garage near Lake Eire, were occupied by a little brown myotis nursery colony with emergence counts averaging 1,400 (adults and fledged young) between 2000 and 2008. In 2010, it fell to 991, but recovered to 1,296 by 2012. Then, in 2013 it fell to 453 and averaged just 50 annually through the summer of 2015. I personally counted 41 on August 28, 2016, a 99% decline.

These bats had been carefully protected from disturbance, so WNS was the only suspected threat. Those that remained appeared to be optimally fat for the season, though I did not attempt to handle them. Curious to see what would happen if these bats remained undisturbed, I invited bat biologist, Jonathan Townsend, to organize a local team to make two emergence counts per summer. In 2017, on July 21 and August 5, counts were 87 and 75 respectively (all volant). In 2018, on June 21, 93 emerged, with 35 pups left inside for a total of 128 bats. On July 19, 144 emerged, and 8 remained inside, for a total of 152.

Southwestern New York nursery colony survivors of WNS, fat and apparently in good health on August 28, 2016.

Though this colony remains far below its pre-WNS average, its current rate of juvenile survival and apparent recovery is remarkable. Perhaps there are conditions, not yet adequately considered, under which small colony size may improve survival odds, for example by reducing competition for food. While massive insect numbers are often available soon after sunset, there are limits to how many a bat can eat in quick succession. Later, insect availability can decline dramatically, possibly forcing young bats to face far stiffer competition than yet realized.

Bat houses in southwestern New York that, prior to the arrival of WNS, sheltered a thriving nursery colony of 1400 little brown myotis.

With surprisingly high frequency, bats banded at the largest, most successful remaining nursery colonies reportedly have disappeared to unknown locations in winter. (6) (7) This raises potentially important questions. Is it possible that prolonged, or too frequently repeated, research disturbances in hibernation sites are contributing to decline and/or hindering recovery? Alternatively, could these bats be finding superior hibernation sites that could one day be lost for lack of awareness among conservationists?

Fortunately, with a bit of hindsight, the WNS response is improving in the Northeast. There are now moratoriums on research at some previously disturbed hibernation sites, and state policies are shifting toward limiting hibernation disturbance to 2 or 3-year intervals. Both New York and Pennsylvania have posted strong warnings against disturbing potentially WNS-infected bats, noting that even mild disturbances can cause death. And this is increasingly recognized as equally true regardless of intent. Most states reported attempts to reduce hibernation disturbance, especially at important locations. In 2018, New Jersey announced a 3-5 year moratorium on research entries at its most important hibernaculum.

Unfortunately, in a rush to stop the spread of WNS or find a cure, some of the most important early assumptions were never tested. It was assumed that prevention of possible mass extinctions justified dramatic increases in previously banned disturbance. It was also assumed that prevention or decontamination of humans entering caves could halt, or at least slow the spread. Neither has proven true. It’s time to rebuild partnerships with cavers who, since WNS arrival have too often been needlessly banned from caves, precluding their ability to help in the discovery and protection of subterranean bat roosts.

Cures have been highly publicized. (8) (9) But successfully treated captive bats have perished from reinfection when returned to the wild. The causative fungus is now well established and long-lived in countless thousands of roosts in caves, rock crevices and tree hollows, most not even discoverable by humans. Imagine the challenge of finding and treating them all! This alone renders eradication of a long-lived fungus hopeless. Just one untreated bat or roost could lead to rapid reinfection of millions. Even worse, any microbe or toxin that could kill the offending fungus could impact countless others, potentially threatening whole ecosystems with unintended consequences.

In our survey, states conducting both summer and winter monitoring of status trends reported equal or greater confidence in summer results that caused minimal or no disturbance. In fact, in one of the most thorough status evaluations yet published Dobony and Johnson (2018) question the need for a cure. They note “that WNS-infected little brown myotis are capable of persisting without human intervention” and that “human involvement could have unknown consequences and even exacerbate population declines.” They conclude “that refraining from intervention currently may be the best option.”

A banded little brown myotis in a Wisconsin mine prior to the arrival of WNS.

This fungus is already widespread in Europe and Asia where bats have apparently evolved resistance and live with it, mostly unharmed. (10) (11) (12) Early evidence suggests that similar potential exists in America. Fortunately, there is growing emphasis on helping surviving bats recover. Acoustic monitoring techniques are being refined for use in tracking landscape-level recovery, (1) (13) (14) (15) and the public is being invited to participate by putting up bat houses and reporting on occupancy. (16)

This is a time of extreme risk for dangerously depleted bat populations. It is also a time for scientists and conservationists to reexamine their priorities. There is an urgent need to minimize all disturbance. WNS kills by forcing costly winter arousals, (17) and research-caused arousals are no exception. This is a time when already stressed bats can least afford to be disturbed. Surviving bats do need help. But in attempting to help, we must exercise great caution to DO NO HARM.

A little brown myotis (Myotis lucifugus) in flight in Wisconsin. One bat can catch up to 1,000 mosquito-sized insects in a single hour.

Bibliography

  1. Observed Resiliency of Little Brown Myotis to Long-Term White-Nose Syndrome Exposure. Dobony, Christopher A. and Joshua B. Johnson. 1, June 2018, Vol. 9, pp. 168-179.
  2. A FIVE-YEAR ASSESSMENT OF MORTALITY AND GEOGRAPHIC SPREAD OF WHITE-NOSE SYNDROME IN NORTH AMERICAN BATS AND A LOOK TO THE FUTURE. Gregory G. Turner, DeeAnn M. Reeder, and Jeremy T. H. Coleman. 2, 2011, Bat Research News, Vol. 52.
  3. An Emerging Disease Causes Regional Population Collapse of a Common North American Bat Species. Winifred F. Frick, Jacob F. Pollock, Alan C. Hicks, Kate E. Langwig, D. Scott Reynolds, Gregory G. Turner, Calvin M. Butchkoski, Thomas H. Kunz. 5992, August 2010, Science, Vol. 329, pp. 679-682.
  4. Nathan J. Salik, Anne M. Vardo-Zalik, Calvin M. Butchkoski. Hibernating Bat Species in Pennsylvania use Colder Winter Habitats Following the Arrival of White-nose Syndrome. Conservation and Ecology of Pennsylvania’s Bats. s.l. : Pennsylvania Academy of Science, 2016, pp. 181-199.
  5. Melinchuk, A. Little brown bats in Massachusetts. Ecology program bureau of Planning, Design, and Resource Protection Department of Consercation and Recreation. 2017.
  6. Interannual Survival of Myotis lucifugus (Chiroptera: Vespertilionidae) near the Epicenter of White-Nose Syndrome. Jonathan D. Reichard, Nathan W. Fuller, Alyssa B. Bennett, Scott R. Darling, Marianne S. Moore, Kate E. Langwig, Emily D. Preston, Susi von Oettingen, Christopher S. Richardson, and D. Scott Reynolds. 4, 2015, Northeast Nat (Steuben), Vol. 21, pp. N56–N59.
  7. Interannual Survival of Myotis lucifugus (Chiroptera: Vespertilionidae) near the Epicenter of White-nose Syndrome. Reichard J.D., N.W. Fuller, A.B. Bennett, S.R. Darling, M.S. Moore, K.E. Langwig, E.D. Preston, S. von Oettingen, C.S. Richardson, and D.S. Reynolds. 4, 2014, Northeast Nat (Steuben), Vol. 21, pp. N56-N59.
  8. Battling a deadly bat fungus. Hiolski, Emma. 15, 2018, Chemical & Engineering News, Vol. 96.
  9. Extreme sensitivity to ultraviolet light in the fungal pathogen causing white-nose syndrome of bats. Jonathan M. Palmer, Kevin P. Drees, Jeffrey T. Foster, Daniel L. Lindner. 9, 2018, Nature, Vol. 35.
  10. White-nose syndrome fungus introduced from Europe to North America. Leopardi S., Blake D., Puechamaille S.J. 6, 2015, Current Biology, Vol. 25, pp. R217-R219.
  11. White-nose syndrome fungus in a 1918 bat specimen from France. KM., Campana MG. Kurata NP. Foster JT. Helgen LE. Reeder DM. Fleischer RC. Helgen. 2017, Emerging Infectious Diseases, Vol. 23, pp. 1611–1612.
  12. Phylogenetics of a Fungal Invasion: Origins and Widespread Dispersal of White-Nose Syndrome. Kevin P. Drees, Jeffrey M. Lorch, Sebastien J. Puechmaille, Katy L. Parise, Gudrun Wibbelt, Joseph R. Hoyt, Keping Sun, Ariunbold Jargalsaikhan, Munkhnast Dalannast, Jonathan M. Palmer, Daniel L. Lindner, A. Marm Kilpatrick, Talima Pearson, Paul S. Keim,. 6, 2017, mBio, Vol. 8, pp. e01941–e01917.
  13. Declines in summer bat activity in central New England 4 years following the initial detection of white-nose syndrome. Brooks, Robert T. 11, 2011, Biodiversity and Conservation, Vol. 20, pp. 2537-2541.
  14. Patterns of acoustical activity of bats prior to and following white-nose syndrome occurrence. Ford WM, Britzke ER, Dobony CA, Rodrigue JL, Johnson JB. 2011, Journal of Fish and Wildlife Management, Vol. 2, pp. 125-134.
  15. Going, going, gone: the impact of white-nose syndrome on the summer activity of the little brown bat (Myotis lucifugus). Yvonne Dzal, Liam P. McGuire, Nina Veselka, and M. Brock Fenton. 3, 2010, Biology Letters, Vol. 7, pp. 392-394.
  16. Nathan J. Salik, Anne M. Vardo-Zalik, Calvin M. Butchkoski. Pennsylvania’s Appalachian Bat Count: Trends from Summer Roost Surveys and a Comparison of Surveys Before and After the Arrival of White-nose Syndrome. Conservation and Ecology of Pennsylvania’s Bats. s.l. : Pennsylvania Academy of Science, 2016, pp. 153-166.
  17. Frequent Arousal from Hibernation Linked to Severity of Infection and Mortality in Bats with White-Nose Syndrome. Reeder DM, Frank CL, Turner GG, Meteyer CU, Kurta A, Britzke ER, et al. 2012, PLOS.

 

Update on Combating White-Nose Syndrome
By Merlin Tuttle
4/10/18

What We’ve Learned

Bats, not humans, are the primary spreaders of the introduced fungus (Pseudogymnoascus destructans) that causes WNS. It cannot be stopped or cured. European bats already have become highly resistant, likely having rebuilt after an earlier attack. In America, in just a decade WNS has decimated highly susceptible, cave-hibernating species. But tiny remnants have survived and could, with protection, rebuild, as appears to have happened in Europe. They are now at a critical juncture, especially vulnerable to disturbance and climate change. Without protection extinctions are possible.

White-nose syndrome (WNS) impact on bats - photo by nancy heaslip
WNS infected bats.

Saving the Survivors

The first rule of medicine is to do no harm. Remnant populations of species known to be at risk should be protected from all roost disturbance, and unfavorably altered temperatures at key hibernation caves of past use should be restored. The costs of public education, protection, and restoration of a relatively few critical caves are minimal compared to those of creating new endangered species.

Long-term WNS monitoring in Pennsylvania led to the following warning. “All survivors still become infected annually. It is likely that these few survivors are existing on limited fat reserves, and every disturbance is an additional cost on those reserves. The effect of this disturbance may directly cause mortality later in the hibernation season to adults or juveniles fighting infection, or it may lower the fitness of adult females enough to inhibit their ability to successfully reproduce.”  

There is no justification for further roost disturbance “to save bats” from WNS, especially during hibernation. Status can be monitored in summer without disturbance, and the search for a cure is by now irrelevant.

I’m encouraged to see trends toward non-intrusive summer monitoring and gradual progress in governmental reopening of caves unneeded by bats but unnecessarily closed to caver visitation. The future of America’s cave-hibernating bats, and caver partnerships in their conservation, requires major policy changes. Thus, on February 15, I joined National Speleological Society President, Geary Schindel, and Chair of the Directorate, Peter Youngbaer, in signing a request for change. Our letter was addressed to Secretary of the Interior, Ryan Zinke, and Secretary of Agriculture, Sonny Perdue.

WNS provides clear justification for long over-due summer monitoring and for public education and involvement. Home owners must be taught bat values and should be encouraged to take pride in putting up bat houses, conducting seasonal emergence counts, and reporting changes to state wildlife agencies. Finally, cavers should once again be encouraged to help identify, protect, and restore long abandoned cave roosts of potentially key importance.

You can help. When federal, state, or private organizations announce support for WNS projects that disturb roosting bats, especially in winter, politely share your concern that such well-intended efforts likely will do more harm than good. Suggest that instead, resources targeted to winter surveys and searches for a cure be redirected for protection of roosts and for non-invasive monitoring of population status trends.

Where key roosts of the past have been abandoned due to altered temperatures or human disturbance, they should be restored and/or protected. Also, standardized active-season surveys are much needed. The State of Pennsylvania, for example, has established protocols for both acoustic monitoring on consistent transects, and for summer roost emergence counts, that can provide opportunities to encourage public participation.

 

Recommended Reading

Zalik, N.J., A.M. Vardo-Zalik, and C.M. Butchkosky. 2016. Pennsylvania’s Appalachian bat count: Trends from summer roost surveys and a comparison of surveys before and after the arrival of white-nose syndrome. Pp. 153-166 in Conservation and Ecology of Pennsylvania’s Bats (C.M. Butchkoski, D.M. Reeder, G.G. Turner, and H.P. Widden, Eds.), Pennsylvania Academy of Science.

Johnson, J.S., M.R. Scafini, B.J. Sewall, and G.G. Turner. 2016. Hibernating bat species in Pennsylvania use colder winter habitats following the arrival of white-nose syndrome. Pp. 181-199 in Conservation and Ecology of Pennsylvania’s Bats (C.M. Butchkoski, D.M. Reeder, G.G. Turner, and H.P. Widden, Eds.), Pennsylvania Academy of Science.

The book, “Conservation and Ecology of Pennsylvania’s Bats” is available at Speleobooks and is highly recommended.

 

How Disturbance Harms Hibernating Bats

How to Restore WNS-Depleted Bat Populations

 


 

White-Nose Syndrome: Origin, Impact and Management

By Merlin D. Tuttle
5/1/16

White-nose syndrome (WNS) is caused by a fungus, Pseudogymnoascus destructans (formerly known as Geomyces destructans). It was first recorded from a photo taken in a cave in Schoharie County, New York in 2006. By the summer of 2014, it had spread across most of eastern North America (25 states and 5 Canadian provinces). In 2015 it reached Nebraska and in early 2016 had also been detected in Washington State.

It appears to have come from Europe via accidental introduction. But we still don’t know how it arrived. It has been hypothesized to have come on the shoes or clothing of a person who contacted it in a European cave, then visited a commercial cave in New York. However, in attempting to explain its sudden appearance in Washington State, Dr. William Halliday has pointed out a possibly more plausible explanation. He notes that, in both New York and Washington, the first sick bats were found within about 30 miles of a major shipping terminal where large quantities of freight are unloaded from Europe and Asia, and that bats have been known to “hitchhike” in large storage containers. It will be interesting to see if fungal cultures from Washington State versus New York can shed light on this intriguing question.

In eastern North America WNS has killed up to 90% of some species that hibernate in caves (especially little brown bats, northern long-eared bats and tricolored bats), with death tolls ranging in the millions. Other cave-hibernators, such as endangered Virginia big-eared and gray bats, seem to be unaffected. Additionally cave-dwellers that don’t hibernate, as well as tree-dwellers appear to be unaffected.

Infections cause bats to arouse too often from hibernation, exhausting limited fat reserves before they can feed again in spring. Though not yet proven, it seems likely that mortality will be heaviest where winters are longest.

Though WNS has had devastating impact on populations of bats that hibernate in caves, it also has provided an unprecedented opportunity to educate millions of Americans regarding the values of bats as insect predators and has stimulated the first widespread summer monitoring of status trends.

It is important to note that European bats appear to have already developed resistance to this fungus. And available evidence suggests that, with careful protection, small numbers of survivors in America will also be able to slowly rebuild immune populations.

I believe we are well past the point of stopping or even slowing this now widespread infection. The guiding principle must be “first, do no harm.” Killing infected bats is pointless, and attempting to decontaminate natural roosts with toxins or foreign organisms could result in disastrous unintended consequences. Finally, treating individual bats is impractical at more than a small, local scale, and it remains to be seen whether treated individuals will then be resistant to reinfection.

 

Our best remaining options are to: 1) strictly avoid further winter disturbance, 2) increase year-round protection of all roosts, 3) educate the public to overcome fear and understand the values of conserving bats and 4) promote minimally invasive research to better understand bat needs and status trends.

 

Aside from strict protection of bat roosting sites, especially in winter, there appears to be no further justification for closing caves. Organized cavers have proven themselves to be invaluable leaders in detecting sites in need of protection, in building and monitoring protective gates and in informing state, federal and private managers of vandalism. We owe a special debt of gratitude for their invaluable cooperation and leadership despite the fact that this crisis often has excluded them from their favorite places.

 


 

White-Nose Syndrome: New Policies Needed for Cave Management
By Merlin Tuttle
10/11/16

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A field team is measuring bat roost stains in a limestone cave in Mexico to assess its approximate past importance to bats. Domed ceilings in warm caves are often extra darkly stained and etched due to heavy use by nursery colonies.

As reported in my keynote address at the 46th annual meeting of North American bat researchers last week, despite our best efforts, WNS has spread rapidly from coast to coast, and there is nothing we can do to stop, slow or find a safe, effective and practically applicable cure. It is here to stay, and eventually will reach every species and habitat that is susceptible. Bats are spreading it far more effectively than humans ever could. It is time to refocus our efforts on helping the few survivors rebuild resistant populations, as apparently has already happened in Asia and Europe.

The overwhelming response from colleagues was that it is time to refocus our efforts on providing the best possible protection at a time when populations are at critical lows. Each winter entry into a bat hibernation site forces at least partial arousals, adding a potentially insurmountable burden to already life-threatening energy losses caused by WNS. No matter how well intended, we can’t afford to risk becoming the proverbial straw that broke the camel’s back.

This small bachelor group of Fringed myotis (Myotis thysanodes) likely has moved more often or has used this site for a shorter period, so its stains are less pronounced.

I was encouraged to speak with several colleagues at the conference who are already documenting apparent recovery of protected colonies of little brown myotis (Myotis lucifugus) in the Northeast. Though this is one of the hardest hit species, current studies are documenting apparent reproductive success and gradual recovery. That’s very encouraging!

It is time to focus all possible resources on protecting surviving remnants from unnecessary disturbance. It is also time to acknowledge that closing all caves, even those never used by bats, is counterproductive, needlessly risking partnerships with cavers that we can’t afford to lose.

These stains illustrate an important characteristic of bat versus mineral stains. Because bat stains result from contact with bat bodies, they are always darkest on distal surfaces, lightest in recessed areas less in contact with bat bodies. In contrast, mineral stains tend to be as dark or darker in recessed areas. Dark stains are most often associated with warm roosts used in summer. They also occur in extra warm parts of hibernation caves, where bats go when awake.

Members of the National Speleological Society have been extremely cooperative during this multi-year period in which access to many of their favorite caves has been denied in hope of slowing the spread of WNS. They have played key roles, contributing financially in addition to helping researchers and resource managers find and protect key sites. Nevertheless, broad cave closures clearly have failed. Though reasonable precautions to avoid disturbance in caves suitable for bat occupancy should continue, there are no further reasons to restrict cavers from using caves which are not suitable for bats.

 

 

 

 

 

So how does one differentiate between caves suited for bat use versus those that are not?

In the coolest climates caves are seldom used except for winter hibernation, and the opposite is true in the warmest climates. Southern caves are used mostly for rearing young. In intermediate climates, a few typically multi-entrance caves may provide effective cool or warm air traps, and to the extent that their volume is sufficient to trap large quantities of cold or warm air that remains relatively stable, they may provide ideal sites for hibernation or rearing young.

Where roosts have been used for very long periods, especially by nursery colonies in domed ceilings, the limestone becomes etched by CO2 from the bats’ breath, combined with wear from clinging claws. In such locations the harder, distal portions of the limestone surface also become extra darkly stained, sometimes also polished.

Throughout mid-latitudes, where a large proportion of North America’s caves are located, fewer than 10 percent are important for either hibernation or nursery purposes. However, at extreme northern or southern latitudes, large proportions of caves may be important for bats in winter or summer only. A few also may be important as migratory stopover sites.

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Some caves harbored truly massive numbers of bats prior to the arrival of human disturbance. This one in northern Mexico shows clear staining and guano evidence of past use by an enormous colony of Brazilian free-tailed bats (Tadarida brasiliensis), one that almost certainly numbered in the 10s of millions. The staining continues for more than a quarter of a mile (0.4 km). Locals report having extracted a truckload of guano daily for more than 20 years.

The largest, most complex caves, with the largest (especially multi-level) entrances have traditionally sheltered the biggest and most diverse bat populations, mostly because they provide the widest range of temperatures, especially important during times of climate change. Any mid-latitude cave that traps and holds large volumes of exceptionally cold or warm air likely has been critically important for bats in the past. Large volume also means improved survival due to less unpredictable fluctuation. When bats are no longer using such caves, it is normally due to human disturbance or changes that have altered air flow unfavorably.

 

 

 

 

 

 

 

 

 

 

 

 

How does one determine historical bat use?

In a large proportion of caves, past use can remain clearly visible for hundreds of years after bats have been extirpated. Most limestone is light in color and is typically stained a rusty reddish color by prolonged bat use. With a little experience bat roost stains are typically easy to recognize. Caves where limestone is too hard or soft for leaving long-lasting stains are rare in North America. Old guano deposits, if not completely obscured by human traffic, may prove additionally useful.

0010740-edit
Roost stains in bat hibernation caves are typically lighter and less etched into the limestone compared with those left by active summer colonies. However sites of extra long and intense use sometimes show conspicuous evidence. Stains left by hibernating bats are often on vertical walls in extra stably cool caves that efficiently trap and store cold winter air without freezing. These Indiana myotis (Myotis sodalis) are hibernating in a marginal cave where numbers are declining.

By measuring areas of bat-stained limestone it is possible to make ballpark estimates of past population sizes. Most cave-roosting bats of North America cluster at densities of roughly 200 or more bats per square foot, so by measuring the approximate area of staining, and conservatively multiplying the area times 200, one can gain rough estimates of past population sizes. Certainly, when hundreds, or thousands of square feet are stained, that would indicate a past mother-lode roost for bats.

Even when no bats remain in such a cave, large populations often can be rebuilt if protected from disturbance, and human alterations to air flow are remedied. Cavers are typically the first to discover and report such evidence and already have proven invaluable in restoring some of America’s largest bat populations. This is a time when such cooperation is especially important, potentially contributing greatly to the recovery of cave-dwelling species.

Gray bats (Myotis grisescens) hibernating in Pearson Cave, Tennessee.
These gray myotis (Myotis grisescens) have only moderately stained and etched surfaces at this roost, used since human disturbance forced them to move from a cooler, preferred roost in the same cave.

It is tempting to point out that in North America’s richest cave areas, most caves are unused by bats, and that those used are normally occupied only in summer or winter. Unfortunately, it is the largest, most complex caves that are often the most sought after by both bats and cavers. Nevertheless, when wise managers and cavers cooperate, they will often find that even in these complex caves, bats only need relatively small proportions in any given season, and that parts can remain open to responsible caving during specific times or even year-round.

For example, the famous Fern Cave in northern Alabama includes miles of passages critical to hibernating bats as well as miles of passages of extraordinary interest to cavers but not to bats. For more than 20 years, responsible members of the Huntsville Grotto of the National Speleological Society played a critical management role through a cooperative agreement. As site managers, they

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This is an example of heavy use of a limestone crevice, over many years, by a small group of bats. Notice the heavy etching and dark staining at the edge, where bats can most easily cling to the surface. The staining gradually fades with increasing distance from the crevice.

regulated access in a manner very helpful to responsible cavers, to more than a million hibernating bats and to the U.S. Fish and Wildlife Service (the owner responsible for its protection).

The agency lacked the manpower and resources necessary to provide adequate protection for this remote property, so were happy to have onsite help from the Huntsville Grotto. Organized cavers were present year-round in the parts unused by bats, and near enough to check the entrance to hibernation areas for possible vandals or other problems. They also were able to use the bat area during the bats’ summer absence. Cavers provided the eyes and ears the Service lacked and did an exemplary job of ensuring that only authorized, supervised entry occurred.

One hundred thousand gray bats hibernating at 32 degrees F in Pearson Cave, Tennessee.
One hundred thousand gray myotis hibernating at 32 degrees F (O degrees C) in a Tennessee cave. These bats roost in an incredibly stable cold air trap just 50 feet (15 m) from the cave entrance only when they remain undisturbed for several years. When disturbed they move to inner areas and decline in numbers due to the increased cost of hibernation at higher temperatures.

Unfortunately, when WNS became a threat, the cooperative management agreement was canceled, and no further entry by organized cavers into any part of the cave was permitted. The subsequent lack of regular monitoring by trained grotto members resulted in extensive vandalism when the government was unable to protect it from entry by an uninformed public. Moreover, the official closure appears to have had no effect in preventing the arrival of WNS. I hope this sad lesson will serve as an example of the importance of cooperation between cave owners and managers and responsible members of organized caving groups.

For further WNS information:

How to restore WNS-depleted bat populations

How Cave Disturbance Harms Hibernating Bats

Finding, Protecting and Restoring America’s Historic Bat Caves

MTBC Blog posts 

 

10 thoughts on “White-Nose Syndrome

  1. What about the use of the naturally occurring soil bacteria that two researchers in Missouri were testing? It is said to inhibit the growth of the fungus, stopping it from sporing out and attaching to the hibernating bats. I heard about this from a researcher in a Missouri while I was giving a bat educational talk at Onadaga State Park.

    1. The price is so low because we basically donated my photos and charged minimal amounts for my work as Science Editor to ensure affordability. Books that are unafordable seldom have impact in reaching those who need them most.

      Even if the soil bacteria killed orimpeded the fungus, it has already been spread into literally millions of locations by infected bats. It’s impossible to treat all those locations, and to miss one would enable renewed spread with still lethal consequences.

    2. In the only study there that I am aware of, successfully treated bats became reinfected when returned to the wild with no evidence of long-term success.

  2. Merlin,
    I’m blown away by the price for the new book. In this day of overpriced books, it’s great to see one that everyone can afford. Also, great plug for the PA book. Thought you would like it. Took awhile to complete.

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