According to Tanner, scaling bark was the Ivory-billed Woodpecker’s primary foraging strategy during breeding season in Louisiana. Tanner wrote that the ivorybill is “capable of easily scaling away heavy bark that other woodpeckers could not loosen.” (Tanner 1942). All woodpeckers in genus Campephilus have specific anatomical characteristics that enable them to forage in this specialized way (Bock and Miller 1959). Following Tanner, most post-Singer Tract search efforts have looked for feeding sign as an indicator of presence. Because Tanner’s descriptions are somewhat vague and many of the photographs showing feeding sign are poor, these efforts have tended to focus on decay state and bark adhesion without taking bark characteristics and tree species sufficiently into account. I posit that tree species and bark and wood characteristics are key factors that should be considered. I further posit that extensive bark scaling on live and recently dead hickories (genus Carya) may be beyond the physical capacity of the Pileated Woodpecker.
As all regular readers know, I’ve been somewhat obsessively focused on bark and bark scaling since my earliest years of ivorybill searching. The reason for this interest is simple: it’s how Tanner found ivorybills or inferred their presence when he couldn’t find them (Tanner 1942). Unfortunately, as discussed in a number of posts, Tanner’s descriptions are somewhat opaque, and most of the published images of feeding sign, including those in the monograph, are not very illuminating. Indeed, some of them are consistent with pileated work that we’ve documented. Plate 8, shown below, is a prime example. The caption reads, “Ivory-bill feeding sign on a slender limb”.
Early on in my study of this subject, I hypothesized that certain kinds of bark scaling on hardwoods might be beyond the physical capacity of the Pileated Woodpecker. I still believe this to be true, a view that is supported by what we’ve documented for pileated and by numerous examples of pileated scaling from online sources. At the same time, the details of what types of work might belong in this category have shifted somewhat, especially as it has become clear that Pileated scaling can look like what’s shown in Plate 8 and that pileateds will scale bark from recently dead sweet gums.
This is not to suggest that ivorybills never scale small and medium-sized branches in a similar manner. According to Tanner they did so frequently; however, I have been focused on what may be diagnostic for ivorybill. It seems likely that there is considerable overlap between ivorybill and pileated work when smaller branches are involved (at least on sweet gums).
The sequences we obtained showing pileateds scaling a sweet gum limb have inspired me to look more deeply at the characteristics of hardwood bark and pursue some research avenues that I hadn’t considered previously. I’ve linked to some of the sources in recent posts, but I’ve had some additional insights that seem important enough to share. Every time I think I’ve run out of things to say on the subject, something new crops up.
Like virtually everyone else, I’ve followed Tanner and focused on two bark characteristics, “tightness” and thickness, but it recently struck me that other features might be important as well. And the literature, mostly from the lumber industry, supports this idea.
Tanner suspected that the Singer Tract ivorybills preferred sweet gums and Nuttall’s Oaks because the bark is thinner, and the thinner barked limbs had “more borers” than thick barked ones. While abundance of food was likely a factor, I suspect that, at least with respect to sweet gums and possibly Nuttall’s oaks, ease of scaling and access to food played a role.
It’s important to point out that in live trees, hardwood bark adhesion varies seasonally, with bark becoming tighter during dormant stages and looser (with considerably less variation from species to species) during the growing season. Bark is often if not always tighter on recently dead trees than on live ones (Stokland et al. 2012).
In addition, “The structural and chemical traits of dead wood, inherited from the traits of living trees, are also major drivers of wood decomposition and these traits vary greatly among tree species.” (Cornellisen et al. 2012). The authors of the linked paper point out that other factors, including size and site, can also contribute to the way that bark loosens post-mortem, but specific traits seem to be paramount, especially since the scaling we deem to be suggestive, whether on standing or downed wood, is on trees that are alive or are recently dead. Because the scaling has a very distinctive appearance, we also deem as suggestive hickory snags and stubs that appear to have been scaled some years ago, even if they are in a considerably later stage of decay overall. Bark attached to hard wood on these longer dead stubs and snags often remains tight for 3 or more years after death.
A 1978 report, entitled Bark and Wood Properties of Pulpwood Species as Related to Separation and Segregation of Chip/Bar Mixtures examined bark morphology and strength properties in 42 different pulpwood species and identified factors that impede the mechanical removal of bark from logs. These include: cellular structure, bark adhesion, bark strength, bark toughness, wood toughness, specific gravity/density, and moisture content. (Institute of Paper Chemistry 1978) One caveat about this report: a subsequent paper gives the sample size for each species, and in many cases (including sweet gums) it was only 2 (Einspahr et al. 1982)
It may be counterintuitive, but the authors found that shagbark hickory was far and away the most difficult bark to remove. (The tightly adhering layer is thin, beneath the dead bark that gives the species its shaggy appearance.) One key finding was that:
“Morphologically, the presence of fibers increases inner bark strength and, when sclereids (a type of cell) are present, bark strength is decreased. Inner bark strength, in turn, has a major influence on hardwood wood/bark adhesion. The multiple regression equation employing wood toughness and inner bark strength accounts for 72% of the wood/bark adhesion variation encountered.”
Sclereids are virtually absent in hickories (Nanko 1980) and a few other species that don’t approach the hickories in bark strength and bark and wood toughness (Eastern cottonwoods, yellow poplars, white ashes, and black willows). These tables are particularly illustrative:
Shagbark hickories are the extreme outlier in this study, in terms of adhesion, as well as in terms of inner and outer bark toughness and strength; there are very few shagbarks in our search area, and we have never found scaling on one. I have been unable to find specific information about bitternut hickory bark strength or toughness, but the industry’s debarking problem applies to all species in the genus Carya due to the near absence of sclereids in conjunction with the other factors. Moreover, the industry does not differentiate among hickory species (Timber Mart South 2016). This 1996 paper is worth quoting at length in this regard (full text is not readily accessible):
The amount of published literature dealing with hickory debarking is very limited. Often it is only mentioned as an example of one of the hardest tree species to debark. One study quantified this by measuring the strength of the bark-to-wood bond of 42 hardwood species, including hickory. According to Einspahr et al., the dormant season bark-to-wood adhesion for hickory is greater than 3000 kPa, which is a tenfold difference from the growing season and nearly three times as great as the dormant season wood/bark adhesion for quaking aspen (Populous tremuloides, L.), a species considered to be extremely difficult to debark in the northern United States.
Einspahr et al. also microscopically examined the failure zone in an attempt to correlate morphological differences with bark-to-wood adhesion. For hardwoods in general, they found that during the growing season, failure occurred in the cambium or in the xylem just inside the cambial zone. Conversely, dormant-season failure occurred in the inner bark. They also found that fibers in the bark increased the inner bark strength while sclereids decreased inner bark strength. Hickory bark can contain between 15 to 20 percent fiber and contains less than 0.05 percent sclereids.
While these studies have confirmed that hickory is difficult to debark, they have not addressed possible solutions to the problem. As a result, hickory is often left behind during harvesting, reducing the total usable fiber from a given stand and, over time, increasing the percentage of the species in the hardwood resource, compounding the problem of future harvests.
When a tree dies, the bark eventually loosens and detaches naturally as the cambium decays. After felling, the cambium remains alive until it has consumed all available food or dries out. Moisture loss, while causing cambial death, initially greatly increases the strength of bark attachment because additional bonding between fibers occurs as the secondary valence bonds with water are broken (Belli 1996).
Thus, even though hickory bark adheres less tightly than sweet gum bark during the growing season, it seems likely that it’s harder to scale year round, given its much greater wood and bark strength and toughness. It is also clear from my observations that sweet gum bark loosens far more rapidly than hickory bark post mortem. Note that we have found fresh scaling on both live and recently dead hickories.
Based on specific gravity of the bark – averaging 0.72 for shagbark and 0.60 for bitternut – and bark moisture content – averaging 34% of dry weight for shagbark, and 60% for bitternut – it seems likely that bitternuts are somewhat easier to debark than shagbarks but considerably harder to debark than virtually any other tree species in our search area.
Comparing bitternut hickories to other species, most oaks have a considerably higher average moisture content in their bark (Chestnut and Southern red, including Nuttall’s oaks, are exceptions) and similar specific gravities. Sweet gum bark has an average specific gravity of 0.37 and an average moisture content of 91% of oven dry weight. (Schlaegel and Willson 1983, Miles and Smith 2009). But oaks and sweet gums have sclereids, and sweet gums and all tested oak species score far lower on bark toughness and strength than shagbark and, by inference, bitternut hickories. Sweet gums and the tested oak species are fairly similar in these regards, but I suspect that the higher density and lower moisture content in oak bark makes it harder to scale and may mean that oak bark adheres more tightly than sweet gum bark for a longer period after death.
I posit that when it comes to woodpecker scaling, dormant season bark adhesion, inner and outer bark strength, and inner and outer bark toughness are all relevant factors. We know that Pileated Woodpeckers remove sweet gum bark with some difficulty and that even on medium-sized limbs, they are not consistently able to remove bark cleanly down to the sapwood. It’s also clear that bitternut hickory bark is very difficult to remove, second only to shagbark hickory in our search area. This further reinforces my view that the work on hickories is not the work of Pileated Woodpeckers.
Click here and here for examples of the hickories that are scaled in a manner we hypothesize is diagnostic for Ivory-billed Woodpecker. Also be sure to watch this YouTube video of a Crimson-crested Woodpecker (Campephilus melanoleucus) foraging. (Thanks to Phil Vanbergen for finding the clip and the scaled hickory at the second link.) I’m reposting the link to the video here because I think it very clearly illustrates many of the characteristics we associate with Ivory-billed Woodpecker work on hickories, although the species of tree being fed on is unknown. Note the striking similarity in appearance and also that the work of the substantially smaller billed Crimson-crested is not as clean around the edges as the work we’re ascribing to ivorybills.
There were no bitternut hickories in the Singer Tract, but there were congeners – pecans and water hickories. Tanner observed ivorybills scaling on these species twice and digging once. For pileateds, there were 4 instances of digging and none of scaling, as opposed to 5 scaling and 9 digging on sweet gums. The relative abundance of water hickory and pecan at Singer was 2.7%; approximately 10% of the trees in our search area are hickories, and hickories are second only to sweet gums in terms of the number of scaled trees we’ve found. While Tanner’s is obviously a minuscule data set, it may support the hypothesis that live and recently dead Carya bark is too tough for pileateds to scale extensively, if at all.
There are a number of hardwood species found in potential ivorybill habitat that are somewhere between sweet gums and hickories in terms of how easily scaled they may be and how soon after death bark decay and loosening set in – eastern cottonwoods, black willows, water tupelos, some oak species, red maples, green ashes, honey locusts, persimmons, and elms – in these species, it seems likely that close examination of the scaling and bark chips can provide some clues.
Previous Ivory-billed Woodpecker searches have focused on bark adhesion and state of decay when considering scaling as possible foraging sign. Bark morphology, dormant season adhesion, inner and bark outer strength, and inner and outer bark toughness, and wood toughness are all relevant to the ease with which bark can be scaled from live and recently dead hardwoods. Specific gravity and moisture content are also factors. Bark from trees in the genus Carya is difficult to remove industrially, and members of this genus are likely the most difficult trees to scale throughout the historic range of the ivorybill. Since Pileated Woodpeckers scale sweet gum branches with some difficulty and do not consistently remove bark down to the sapwood, it may be beyond the physical capacity of Pileated Woodpeckers to scale hickories extensively and cleanly, while leaving large pieces of bark behind. Extensive work on hickories that has a distinctive appearance may be diagnostic for ivorybills; this distinctive appearance of this scaling may also be the key to recognizing Ivory-billed Woodpecker foraging sign on other species.
This may be no more than an aside, but it may be a relevant data point. I recently observed a Pileated scaling briefly on a live 14″ DBH Norway maple in my yard near New York City. The photos show that the sap is flowing. The appearance of the scaling is exactly what I’d expect for Pileated, with strips about half an inch across. Norway maple may be a decent stand-in for sweet gum; while its bark has a higher specific gravity, 53 as opposed to 37, the moisture content of the bark is almost identical, 91% as opposed to 90%.
Bock, Walter J. and Waldron Dewitt Miller, The Scansorial Foot of the Woodpeckers, with Comments on the Evolution of Perching and Climbing Feet in Birds, American Museum Novitates, #1931, 1959
Belli, Monique L., Wet storage of hickory pulpwood in the southern United States and its impact on bark removal efficiency, Forest Products Journal. Madison 46.3 (Mar 1996): 75.
Cornelissen, Johannes H.C., Ute Sass-Klaassen, Lourens Poorter, Koert van Geffen, Richard S. P. van Logtestijn,Jurgen van Hal, Leo Goudzwaard, Frank J. Sterck, René K. W. M. Klaassen, Grégoire T. Freschet, Annemieke van der Wal, Henk Eshuis, Juan Zuo, Wietse de Boer, Teun Lamers, Monique Weemstra, Vincent Cretin, Rozan Martin, Jan den Ouden, Matty P. Berg, Rien Aerts, Godefridus M. J. Mohren, and Mariet M. Hefting, Controls on Coarse Wood Decay in Temperate Tree Species: Birth of the LOGLIFE Experiment, Ambio. 2012 Jul; 41(Suppl 3): 231–245.
Einspahr, D.W, R.H VanEperen, M.L. Harder et al. Morphological and bark strength characteristics important to wood/bark adhesion in hardwoods, The Institute of Paper Chemistry, 1982: 339-348.
Institute of Paper Chemistry, Project 3212, Bark and wood properties of pulpwood species as related to separation and segregation of chip/bark mixtures, Report 11, 1978.
Miles, Patrick D. and W. Brad Smith, Specific Gravity and Other Properties of Wood and Bark for 156 Tree Species Found in North America, United States Department of Agriculture, Forest Service. Northern Research Station, Research Note NRS-38, 2009.
Nanko, Hiroki, Bark Structure of Hardwoods Grown on Southern Pine Sites (Renewable Materials Institute series), Syracuse University Press, 1980.
Schlaegel, Bryce E. S and Regan B. Willson, Nuttall Oak Volume and Weight Tables, United States Department of Agriculture, Forest Service. Southern Research Station, Research Paper SO-l 86, 1983
Siry, Jacek, ed., Species Detail Report, Timber Mart-South, 2016
Stokland, Jogeir N., Juha Siitonen, and Bengt Gunnar Jonsson, Biodiversity in Dead Wood, Cambridge University Press, 2012
Tanner, J.T. The Ivory-billed Woodpecker,National Audubon Society, 1942.
Thanks to Fredrik Bryntesson, Steve Pagans, Chris Carlisle, and Bob Ford for their help with this post.
To expand on some of the data included toward the end of the March trip report (which is worth reading in in conjunction with this post), I thought it would be informative to provide a season by season and sector by sector breakdown of the scaling I and others involved with Project Coyote have found since the spring of 2012. To do so, I’ve gone through my notes and photographs and have done my best to reconstruct the data collected. While not complete (I’m quite sure a good deal more scaling was found in Sector 3 during 2013-2014, for example), I think this breakdown is a fairly accurate reflection of what we’ve found over the years.
As discussed in previous posts, I think extensive scaling on hickory boles is the most compelling for Ivory-billed Woodpecker. Bark on this species is thick, dense, and usually remains very tight for a long time. Extensive scaling on sweet gum boles and oaks (upper boles and large branches) is second among work that I’ve found. Work on small boles, and higher and smaller branches is somewhat less compelling and is more significant for its abundance. Some of the high branch scaling and work on smaller boled sweet gums may well have been done by Pileated Woodpeckers (and possibly by Hairy Woodpeckers), but the abundance, the presence of large bark chips in many cases, the way it appears in clusters, and the fact that Pileateds scale infrequently suggest a different source for much of it.
I have excluded all work where squirrels are suspected but have counted one tree, a hickory found this year, on which the work could well have been that of a Hairy Woodpecker. Hairies do forage for Cerambycid beetles just under the bark, but they’re only capable of removing tight bark in small pieces; their work on hickories is perhaps more accurately described as excavation through the bark.
The trail cam images toward the end of this post are the best we have (out of many thousands of hours of coverage) showing how these species forage on suspected ivorybill feeding trees.
All trees were live or recently dead (twigs and sometimes leaves attached). All scaling was on live or recently dead wood.
Sweet Gum (Liquidambar styracifula)
Sector 1: 46
Sector 2: 8
Sector 3: 51
~15% had scaling on boles (a few of these were large trees). The majority of work was on crowns, including larger branches. Fallen trees were included when woodpecker involvement was evident and bark was tight.
Bitternut Hickory (Carya cordiformis)
Sector 1: 3
Sector 2: 4
Sector 3: 7
All trees were standing; scaling was on boles and was very extensive (the tree shown on the homepage is one example) with one exception from this year . Insect tunnels were visible in all examples. An additional hickory with a modest amount of high branch scaling was found in Sector 1 this year but was not counted for this analysis.
Oak (Quercus) spp.
Sector 1: 1
Sector 2: 4
Sector 3: 0
All oaks had scaling on large branches; one also had some on the bole. All oaks in Sector 2 were found in a single cluster.
We have some information on forest composition in Sector 3, and it appears that sweet gums make up approximately 19%, oaks upwards of 35%, and hickories somewhere under 10%. Sectors 1 and 2 may differ and be more varied in overall composition.
The overwhelming preference for sweet gums relative to their abundance stands out. The scaled oaks are a mix of species, one Nuttall’s, one willow, the others unidentified.
In Sector 3, I am treating the compact stretch from the location of Frank Wiley’s sighting last spring/downed sweet gum top where we had the camera trap to just south of our current deployment as a cluster. The estimate of 23 trees being found in this area is conservative. I have only found one instance of recent scaling north of the location of the downed limb/Frank’s 2015 sighting. The main cluster has been in the same vicinity this year and last, with additional work scattered around farther south. Two of the hickories are within 30 yards of each other, approximately half a mile from the cluster, and one was on the edge of the concentration.
It also may be significant to note that we found a cluster of old but intriguing cavities in the same vicinity as the Sector 3 concentration in 2013-2014. Most of these seem to have fallen. The difficulty we’re having finding active, suggestive cavities is vexing, and may be the most compelling reason to be skeptical about the presence of ivorybills in the area. At the same time, finding Pileated cavities is difficult, even in defended home ranges.
I’m treating Sector 1 as a single concentration; the vast majority of the work is on a natural levee where sweet gums are abundant. The entire area is considerably larger than the other clusters, but given the abundance and ease with which we’ve found sign there over the last five seasons, I think it constitutes one area of concentration.
In Sector 2, there was a small cluster in the area where I recorded putative kent calls in 2013, with work found in 2012 (spring and fall) and 2013. Because the area is small with open sight lines, I can be confident there has been no recent work there since late in 2013 (I last passed through it with Tom Foti back in March of this year.)
The sweet gum work Tom and I found on that day was perhaps half a mile north of this cluster, within 100 yards of the hickory on the homepage. The other hickories found in the 2013 and 2014 seasons were not far away, no more than 500 yards apart as the crow flies.
There’s obviously some bias here, since there’s a relationship between finding feeding sign in a given area and spending time there. Nevertheless, I have little doubt that the putative ivorybill work tends to be clustered. I also have little doubt about the strong preference for sweet gums, since I’m not looking at tree species when I look for scaling. The degree to which sweet gums are favored has only become clear over the last year or so.
Frank pointed out this data does not reflect most of the scaling that likely exists in relatively close proximity to the Sector 3 cluster but cannot be quantified because it is in an area we have intermittently visited due to inaccessibility. Only two or three examples are from this area, which has been visited a handful of times.
In late December 2014, I wrote what I’ve described as a speculative post titled, “Is There a Way to Recognize Ivory-billed Woodpecker Excavation? In that post, I relied on Tanner’s Plate 11,
a brief description from the monograph: “When Ivory-bills dig, they chisel into the sap and heartwood for borers like other woodpeckers, digging slightly conical holes that are usually circular in cross section (Plate 11)”, and online imagery showing the work of other Campephilus woodpeckers. Material found during my recent visits to Kroch library at Cornell lends some support to the ideas contained in that post, and so does T. Gilbert Pearson’s photograph of a tree that had been fed on by ivorybills.
The archival material includes additional images of ivorybill excavation and a considerably more detailed description by Tanner in a document prepared for the Cuban search in the 1980s. The passage includes somewhat more detail on bark scaling than is found elsewhere, but more importantly it describes ivorybill excavations as “hard to distinguish from similar digging by the Red-bellied Woodpecker”.
Courtesy of the Division of Rare and Manuscript Collections, Cornell University Library
This description may seem counterintuitive to some. Despite my own writing to the effect that ivorybill morphology may lead the species to dig less efficiently than pileateds and my references to targeted digging, I still had an underlying assumption that the size of the bird would correlate with the size of the dig and that ivorybill excavation would often resemble the familiar large furrows dug by PIWOs. While a couple of the holes in Plate 11 and in Pearson’s photograph may well involve the merging of more than one dig, it appears that ivorybill excavations are usually more targeted and that large furrows are not typical.
Also of interest for multiple reasons, including the observation of birds scaling very small limbs and of one feeding 5′ from the ground, are Tanner’s field notes from April 3rd, 1937.
I’ll let the remaining images of known and suspected ivorybill excavations speak for themselves and will conclude with a few from our search area that seem consistent with known ivorybill work. While I’m nowhere near as confident about this material as I am about scaling, I suspect that finding excavations that are consistent with what ivorybills are known to have done in conjunction with scaling is suggestive.
I hope this material will be useful for other searchers. All images from the Singer Tract below are courtesy of the Division of Rare and Manuscript Collections, Cornell University Library. Most of these images were published in Tanner’s dissertation but have not been widely disseminated.
And now some examples from our search area that resemble the existing images of known ivorybill excavation. This is not something I’ve focused on, so I’ve probably missed other examples.
There will be one or two more installments in this series, but the next post is likely to be a trip report, probably the last for this season.
Careful examination of bark chips found in conjunction with extensive scaling is one of the key elements in our diagnostic gestalt, but “chips”, a term I’ve been using for years, is both inaccurate and too vague for what we believe is being left behind by Ivory-billed Woodpeckers and for differentiating it from the leavings of other animals. Tanner used “pieces” of bark, ranging “from the size of a “silver dollar to the size of “a man’s hand.” A caption from the National Geographic article on the 1935 Allen and Kellogg expedition that refers to “large chunks of bark”. The existing images of these pieces of bark suggest that chunks is the better term.
It’s important to reiterate that this discussion applies only to live and freshly dead hardwoods. Pines slough bark quickly after death. The process is slower in hardwoods, but as decay progresses, the bark loosens considerably, with the rate of loosening depending on species and environmental conditions. Once the bark has loosened sufficiently, PIWOs can and do scale bark extensively, sometimes leaving behind large chips. In the images that follow (from Allen and Kellogg and Tanner), the bark chips ascribed to ivorybills appear to come from considerably longer dead trees than some of the examples we’ve found, but the images are informative.
The small tree shown above, identified as a “dead gum” by the 1935 expedition, appears to be a hackberry or sugarberry not a gum, and a fairly long dead one; the pieces of bark at the base resemble ones we found beneath hackberries or sugarberries in our old search area, some of which were considerably larger (the one below is the largest).
This colorized slide reveals more about the bark at the base of these pines than the black and white print in Tanner (Plate 9).
There’s also this example, (Plate 10 in Tanner), which appears to be in a considerably more advanced state of decay, and presumably looser, than much of the work we find most interesting. I suspect most of the grubs were placed on the chip for illustrative purposes; the caption “Beetle larvae from beneath bark of Nuttall’s oak” is ambiguous as to where the larvae, which appear to be small Cerambycidae, were actually found.
What I think is most salient in Tanner’s description of bark chips is shape not size. In this regard, it seems important to come up with a more specific set of terms to replace the commonly used “chips”. I’d suggest using chunks and slabs for suspected ivorybill work (although smaller pieces of bark may also be present). Pileated bark removal can involve chips, strips, or flakes, the last when they’re doing the layered scaling discussed here and here. I suspect that squirrels remove hardwood bark primarily or exclusively in strips, and of course, their bark removal on cypresses leaves shredded bark hanging from the trees.
Let’s take a closer look at the differences among pieces of bark we have reason to believe were left by squirrels, those we have reason to believe were left behind by Pileated Woodpeckers, and those we suspect were left behind by Ivory-billed Woodpeckers.
I collected a number of bark chips from the tree we know to have been scaled by a squirrel, and while these were removed before our camera trap revealed the source, there’s strong reason to think they too were left behind by squirrels.
Note the uniformly elongated shape and the ragged appearance at the tops and bottoms of these strips of bark. This is not typical of bark that we infer or know to have been removed by woodpeckers, and it’s consistent with chewing, not scaling. The presumed squirrel strips I collected had the following dimensions:
The downed sweet gum from which they had been removed was a fairly young tree, and the bark is much thinner than on more mature ones. These strips were approximately 1/8″ thick. While this is a very small sample, we suspect (along with Houston from IBWO.net) that approximately 3″ is the upper limit for width when a squirrel is doing the bark removal.
Our research and observations suggest that Pileated Woodpeckers have two strategies for removing tight bark; one involves pecking around the edges until they can gradually pry off small pieces, and the other involves scaling away strips, sometimes in layers. Their physical structure precludes them from doing the extensive, clean scaling of tight bark that Tanner associated with ivorybills.
We suspect that this collection of chips, from a honey locust near a known Pileated nest, reflects the range of what the species is capable of doing on a tight-barked hardwood (and honey locust bark is relatively thin). The upper limit appears to be hand size, with many-quarter sized or smaller.
The following are measurements of some fairly typical suspected Pileated strips from a sweet gum:
The strips shown below, suspected Pileated Woodpecker leavings from a high branch, are on the large end of the spectrum for this category of work. The Peterson Guide is 9.5″ x 6.5″. I can’t rule squirrel out completely for these.
Flakes resemble strips, but they are removed in layers, so that reaching the sapwood is a gradual process. Pileated scaling frequently has this appearance, something that seems frequently to be the case with congeners, including the larger-billed Black Woodpecker (Dryocopus martius).
The chunks and slabs we suspect to be ivorybill work are significantly larger and thicker than strips, flakes and chips, although strips and chips may be present in the mix at the base of suspected feeding trees. Chunks are usually more irregular and varied in size and shape, and both chunks and slabs sometimes have what appear to be strike marks from a broad bill.
I kept one of the chunks scaled from the hickory tree on the homepage, a fairly typical example. It is 8.5″x3.5″ and .375″ thick. (It has undoubtedly lost some of its thickness after drying for over two years.)
The sweet gum chunk with the apparent bill mark Frank is holding is 7.5″x3″ and .25″ thick. On mature, thicker barked trees most or all suspected ivorybill chunks, chips, and slabs will have been removed cleanly, all the way down to the sapwood.
This particular bark “chunk” is intriguing on several levels. We have found that markings many describe as “bill marks” are really truncated galleries between the bark and sapwood. Marks made by woodpecker bills are distinctive, but somewhat subtle, and easily overlooked. This chunk actually has two interesting markings – markings that were left by the animal that removed the bark. The first is near the end of my left thumb – my right index finger is pointing toward it. It is about a quarter inch wide, a bit over a half inch long, and three sixteenths of an inch or so thick. The other is a “V” shaped “notch” at the end of the chunk, near the center of the photo. These places look as if they’ve been struck with a chisel – hard enough to rip the bark away from the sapwood/cambium. This suggests that, even though this bark was very tight, very few strikes were required to loosen and remove it. Granted that these marks are bill strikes, this suggests that the bird removing bark is indeed a powerful animal for its size. Back to Mark.
The two preceding examples are on the smaller side for suspected ivorybill work; in the first, the density, tightness, and grain of hickory bark seem to be a limiting factor on size. Some of the larger examples are shown in the Bark Chip Gallery (as are several of the images shown above). A couple of additional examples of larger slabs are below. In the first, the oak was approximately 8 months dead (leaves attached), and the bark was still tight. (The fractured slab was damaged in transit.)
The first two installments in this series, which was inspired by the discovery that squirrels are doing some of the bark scaling in our search area, are here and here. This installment will consider the appearance of the scaling itself, and the next will focus on pieces of bark; “chips” no longer feels sufficient to describe the spectrum of what we’ve found, and using more specific terminology may shed more light on what we think is diagnostic and why.
I’ll begin with the work we are now presuming to have been done by squirrels. In retrospect, it’s easy for me to understand why I was fooled by this bark stripping. I was not seriously considering mammals as a source due in part to the extent of some of the work involved; I never saw incisor marks on the wood, something that’s often described as being an important indicator; similarly, I have been unable to find these marks in the photographs I’ve taken of stripping that we now presume to have been done by squirrels.
In addition, I was somewhat misled by Plate 8 and the description of what Kuhn thought was diagnostic that his daughter shared with us. (Scroll down in this post to see where my thinking went astray.) It’s my current view that Plate 8 could conceivably be squirrel work. Tanner doesn’t state that he actually observed an ivorybill doing the scaling.
Between 1937 and 1939, Tanner observed actual scaling a total of 73 times, but it’s not clear how many instances he might have photographed. In hindsight, the scaling in Plate 8 is not particularly impressive; the scaled patch is relatively small; the bark is thin and the hanging pieces may be an indication of removal by gnawing rather than bill strikes. Adhering bits of shredded bark and cambium are evident in some of the work we believe to be squirrel, including on the tree where we captured a squirrel stripping bark (albeit much smaller ones in that case).
In fact, I think one of the keys to recognizing that squirrels are likely responsible for removing bark is a ragged, shredded, or chewed up appearance to the bark and cambium, as in the examples below.
The information we got from Mrs. Edith notwithstanding, I am going to examine the edges of scaled areas more carefully and be sure they are for the most part cleanly incised. This is one of the main criteria for ascribing the work to ivorybills (although by no means all Campephilus scaling falls into this category, and some can have ragged edges). As I’ll be discussing in the next post, I think that bark chip characteristics provide an even better diagnostic.
Now let’s turn to targeted digging and the similarities between what we’re finding and the work of other Campephilus woodpeckers. In some of my previous posts on bark scaling I’ve mentioned “little or no damage to the underlying wood”. “Little” is the operative word here. In most if not all of the examples of scaling associated with large Cerambycid exit tunnels that we’ve been able to examine up close, there are also indications of targeted digging, and we have seen similar targeted digging on some of the higher branch work we’ve found. Targeted digging involves the expansion of individual exit tunnels in varying degrees. This can range from what appears to be little more than probing with the bill to deeper and wider excavations, but this excavation is incidental to the scaling, whereas in Pileated Woodpeckers, scaling on tight barked-trees is typically incidental to excavation.
A magnificent series of photographs by Luiz Vassoler posted to the Flickr Campephilus group, showing a Crimson-crested Woodpecker scaling and doing targeted digging, is illustrative (scroll through to your right for the whole series). This is not to suggest that other woodpeckers can’t or don’t dig for larvae in a targeted way, only it’s more suggestive evidence for the presence of Ivory-billed Woodpecker in our search area, given the context and what’s known about the foraging behavior of its congeners.
I’ll keep commentary to a minimum and post some examples from our area (the seven photos immediately below) and then links to work done by other Campephilus woodpeckers.
Pale-billed (on palm):There’s no scaling here, but the exit tunnels have been expanded vertically, and the expansions resemble some of the rectangular ones above.
Pale-billed (at nest): Very targeted digging and slight expansion of some exit tunnels.
Pale-billed: On a scaled surface, some tunnels expanded.
Robust: I’m including this almost as much for how well it shows Campephilus foot structure and the rotation of the fourth toe and hallux.
Cream-backed: Somewhat more aggressive expansion of tunnels on longer dead wood.
Red-necked: Targeted digging to the right of the bird.
Crimson-crested: Elongated dig into exit tunnel.
Crimson-crested: another great shot of the Campephilus foot. Targeted dig at bottom of scaled area.
Crimson-crested: Video showing targeted digging on an unscaled area.
Magellanic: are the most Dryocopus-like in the genus in terms of foraging behavior. Note their smaller bills and relatively shorter necks. They seem to spend a lot more time feeding near the ground and excavating large foraging pits than the other species, but they too do a considerable amount of targeted digging.
Magellanic: The appearance of the scaling here is strikingly similar to what we think is diagnostic for ivorybill. The tunnel at bottom right has been expanded, likely with the tip of the bill. It looks as though there is more targeted digging above and to the left.
The two images below, showing targeted excavations on small limbs, associated with extensive scaling on young, freshly ambrosia beetle-killed sweet gums, bear a striking similarity to work by Crimson-crested (the long furrows in particular) and Magellanic Woodpeckers.
One final and more speculative observation that might be of interest to other searchers. I had dismissed this work on a live maple as likely pileated because it is generalized digging, not scaling. After going through so many images of Campephilus foraging sign, I’m a little more intrigued by it, as I see similarities to sign like this and this. Like some of the work on ambrosia beetle-killed sweet gums, this almost looks like a hatchet had been taken to the tree; the wood was not at all punky; and red maple at 950 on the Janka hardness scale, while not nearly as hard as bitternut hickory (1500), is harder than sweet gum (850). While I’m not proposing this as a diagnostic, it may be more interesting than I initially thought.
Part 1 of this series is here, and the event that led to my writing it is discussed here. I now expect to write 2-3 additional posts on this topic and may create a new page that summarizes the whole series. I’ve hidden the Bark Scaling Gallery page to be reworked later or incorporated into the summary.
This post will reiterate, revise, and expand upon earlier ones dealing with bark scaling and woodpecker anatomy. The next one will focus on certain characteristics of the scaling we think is being done by Ivory-billed Woodpeckers, on finer details that characterize it (based in part on comparison with work done by congeners), and on how to differentiate it from bark removal done by squirrels. The following entry will deal with bark chips in more depth, and from a slightly different angle than previous posts on that subject.
I had originally intended to address the next post’s planned content in this one, but as I started writing, I realized the long but necessary introduction would bury the lede. It soon became clear that I’d have to divide the post in two with this one for background.
The first important point is that woodpecker taxonomy is in a state of dramatic change, so much so that the American Ornithological Union is being advised to place Downy and Hairy Woodpeckers in separate genera and that their current genus, Picoides, should be divided into four. Notwithstanding the taxonomic upheaval, there’s no question that Campephilus woodpeckers and Dryocopus woodpeckers are only distantly related, that their similarities are the product of convergent evolution, and that these similarities are far more superficial – involving size and coloration – than structural or behavioral. Formerly, some incorrect taxonomic assumptions led to the lumping of Campephilus and Dryocopus into the “tribe” Camphelini, an idea that’s discussed and dismissed in the first paper linked to above. This has been one factor in perpetuating some fairly common and persistent misconceptions – that the two species are closely related, that they occupy or occupied the same ecological niche and might be competitors, and that hybridization might be possible (something I hear surprisingly often).
The following differences are relevant to this discussion:
- Bill size and shape. These are dramatically divergent as any comparison shot of specimens makes clear. It’s also worth noting that the three North American Campephili are closely related to each other. DNA analysis suggests the three are distinct species and the Cuban ivorybill may be more closely related to the Imperial Woodpecker than the mainland US species. This study suggested that divergence among the three took place between .08 and 1.6 million years ago. The southern members of the genus are more remote cousins, having diverged approximately 3.9 million years ago. At one time, the southern species were considered a distinct genus, and they have smaller bills, both objectively and relative to body size. Magellanic Woodpeckers have the smallest bills relative to body size in the genus, and their foraging behavior is more Dryocopus-like than their congeners’.
- Neck length. The much longer neck of the ivorybill allows for a broader range of motion.
- Foot and leg structure. Campephilus woodpeckers have a unique variation on what have been called pamprodactylous feet. (Wikipedia and David Sibley both miss the vast difference between Campephilus foot structure and that of most other woodpeckers.) In this genus, the hallux (first) and fourth toe (the rear toes) are both on the outer edge of the foot; the toes can be rolled forward for climbing and backward for perching in a manner that looks more zygodactylous. (The preceding links to images of Sonny Boy, the juvenile ivorybill, and Kuhn are great illustrations.) The fourth toe is highly elongated, the longest toe on the foot, and the hallux, (in the ivorybill, the outermost toe) is relatively longer than in any climbing woodpecker species. The second and third (innermost toes) are angled inward. This is shown quite clearly in a number of the images from the Singer Tract, including Plate 13 in Tanner.
- Dryocopus woodpecker feet are closer to being truly zygodactylous – two in front, two behind, with limited mobility and the hallux as the inner rear toe, although the fourth toe can be rolled outward to some extent; this provides less stability when making lateral blows.
In addition, Campephilus woodpeckers typically climb and forage with their legs both farther apart and higher relative to their bodies than Dryocopus. This enables them to keep their lower bodies closer to the trunk and move their upper bodies more freely, providing more stability for making powerful, lateral blows.
4. Tail structure: the ivorybill’s tail feathers are long, thin, barb-like, and stiffer than the pileated’s. The tail serves as an anchor and also helps allow for a broader range of motion.
5. There other structural differences, including wing shape, but these are the main ones that point to how Ivory-billed Woodpeckers have evolved in a way that makes bark scaling their most efficient foraging modality, whereas Pileateds are far better suited to digging, using a perpendicular motion.
Much of the foregoing is based on Walter Bock’s analysis of woodpecker adaptations for climbing, which was also discussed in depth here. I’ve tried to explain Bock’s key points in straightforward and less technical terms. A longer quote from Bock appears at the end of this post.*
In addition to these structural differences, Pileated Woodpeckers (and to the best of my knowledge all their congeners) regurgitate when feeding young. Campephilus woodpeckers carry food to the nest and appear to be highly dependent on beetle larvae when caring for their nestlings. This means that Pileated Woodpeckers have to ability to take advantage of multiple food sources during nesting season, while Ivory-bills have a more limited range of options. While I don’t think this supports Tanner’s theory of old-growth dependence, it does point to a higher degree of specialization that would impact numbers, range, and suitability of habitat.
At the same time, the anatomical differences and degree of specialization convince me that certain types of feeding sign are beyond the physical capacity of a Pileated Woodpecker and are likely diagnostic for Ivory-billed Woodpecker.
There is a dearth of clear images showing Ivory-billed Woodpecker feeding sign. There are a handful of photographs, most of them very poor. The majority were taken in the Singer Tract and some showing work on pines were taken in Florida by Allen and Kellogg. Few of them depict the high branch work that Tanner described as being characteristic, and when they do, there’s virtually nothing that can be discerned from them. It is also not entirely clear that Tanner’s attribution of feeding sign to ivorybills was always based on direct observation, which makes us wonder whether some of the work might actually have been done by squirrels. Regardless, this makes it difficult to draw inferences from the existing body of imagery.
That said and with awareness of the perils in extrapolating, one lesser known image from the Singer Tract is worth comparing with the work on boles that’s been discussed in multiple posts.
“The Blind at Elm Rock”, Ivory-billed Woodpecker nest tree and detail showing scaling and excavation on trunk. Courtesy of the Division of Rare and Manuscript Collections, Cornell University Library
This is a view of the 1935 nest tree, which was a red maple. It’s taken at a different angle than the more familiar shots, so it shows some large areas of scaling on the bole that the others do not. While I can do no more than infer that this was done by ivorybills, it’s clearly old, and there’s an abundance of excavation in the underlying wood; nevertheless, the edges and contours of the scaling are strikingly similar to the work we’ve found on boles, especially the area at the lower right, just above the intervening foliage.
This is the jagged appearance I described in the previous post; the similarities are most evident in the picture below and on the home page.
Because there are so few informative images of ivorybill feeding sign, the best available option is to look at the work of other Campephilus woodpeckers. Even though they are not as closely related as the Cuban ivorybill or the imperial, their morphology and foraging behaviors are similar; even the work of the smaller-billed but oft-photographed magellanic can provide some clues. I’ll examine this and some probable identifying features of squirrel scaling in the next post, which will take a close look at scaled patches on trees.
*”. . . in most woodpeckers, as, for example, the pileated woodpecker, the legs are held more or less beneath the body,the joints are doubled up,and the tarsus is held away from the tree trunk. This position of the legs is disadvantageous for the bird, because the body is held away from the tree trunk and the muscles of the leg are working at a mechanical disadvantage; the analogy is to the mountain climber who is standing on a narrow ledge with hand holds only beneath his chest. In the ivory-billed woodpecker, the legs are directed away from the center of the body, and the tarsus is pressed against the tree trunk. This method allows the body to be held close to the tree, with the joints of the leg extended. Hence the leg muscles have a mechanical advantage, because they are at the beginning of their contraction cycle and are acting along the length of the segments of the leg. When the body is held close to the trunk, it not only decreases the outward component of gravity but allows the tail feathers to be applied to the supporting surface for a greater distance from their tips. If the bird is climbing on smaller limbs, the feet can encircle the limb and thus obtain better support. However, no matter what size the limb is, the disposition of the legs and the spreading of the toes of the ivory-billed woodpecker furnish direct and powerful resistance to both the lateral and backward motions of the woodpecker when it is at work and, with the tail, furnish a tripodal base of great strength against the pull of gravity.”
I thought it was important to post the following advance of writing a comprehensive trip report.
On arriving in the search area last week, I found fresh scaling on a downed, recently dead sweet gum. The tree was relatively small, with a DBH of under two feet, and was alongside one of the roads that pass through our search area. There was fresh work on it on subsequent days. I staked it out on Thursday and saw nothing. We placed one of our game cams on it on Friday and retrieved it late Saturday. The trail cam photos showed a squirrel removing the bark fairly extensively. These images are currently in the game cam’s proprietary format, and we’ll post them in the near future.
As is the case with many of these blowdowns, there was also work in the tops that looked very consistent with Tanner’s descriptions of ivorybill scaling, although only on the upper sides of the limbs and branches. What this tells us is that we have to think squirrels are likely responsible for scaling on downed sweet gums and that all possible sign on downed wood should be looked at with a jaundiced eye. It also means that my previous foraging preference analysis has to be revised; we’ve taken that page private at least for the time being.
I did not collect any chips that are unquestionably the work of a squirrel, but I did gather several that I presume to be. They measure:
and thus are all considerably longer than they are wide, stripped with the grain rather than scaled. The edges that go across the grain have a ragged appearance, and since the tree was not mature, the bark is thin and brittle compared to the bark of the mature downed top discussed below.
It’s odd that we only started finding this type of work in abundance in the past year; it doesn’t exactly match the diagnostic criteria I’d articulated earlier, but it comes close in some respects. It has been an unfortunate distraction, since the work on downed trees is much easier to find and photograph than work on the boles or upper branches of standing ones.
There was a little bit of fresh work on the downed sweet gum top found in April, but it was not extensive enough even to show up in the game cam images. There were a few chips on the ground, more like strips than chips, actually, 6′ to 8′ inches long and no more than an inch across at the largest. We’ve had numerous images of squirrels on that top but none showing them scaling bark for a period of more than two months. We got numerous images of squirrels again this time, and also a pair of Pileateds, with a Downy or Hairy (we didn’t examine the frames very closely) literally trailing the PIWOs up the trunk. In any event, there was no way to tell what did the little bit of scaling, or what did the scaling on the upper part of the downed top or the left fork, which had been almost entirely stripped before we got the camera on it. I lean toward this little bit of new work was done by the Pileateds, but either way the chips don’t have the characteristics I associate with suspected ivorybill chips.
I had been planning to do a post refining and being more explicit about the different types of work I’d been ascribing to ivorybills. I still plan to go ahead with this project but will have to do so informed by this new information. I expect to write something later this month, after I’ve posted the trip report.
While squirrels cannot be ruled out for some of the work we’re finding, it seems unlikely that squirrels are doing all of it, especially on the boles of dense-barked, mature trees (like the hickory on the homepage and most of the others shown here) that have numerous cerambycid exit tunnels and on those that are not quite so freshly dead (and therefore don’t offer as much nutritional value). We monitored the tree on the homepage for several months and had no evidence of squirrels removing bark.
Some preliminary thoughts on what I think remains likely ivorybill work:
The chips shown in the bark chip gallery are mostly as large as or larger than an adult man’s hands. Chip size, shape, and density are probably factors that need to be looked at very closely, and perhaps the contrast between a very ragged, gnawed appearance and a cleaner one with apparent bill strikes is another key aspect.
This smashed sapling was clearly not worked on by squirrels, and the little patches of targeted digging on the small limb are highly reminiscent of Magellanic sign I’ve seen in several photographs:
If you zoom in on the image below, you can see that a woodpecker was involved because the tunnels have been expanded slightly and there’s one Magelllanic-looking dig on the smaller limb. This one also has some superficial scratches that could be from a bill:
This work on a dead oak from the old search area remains interesting, because the bark chips were huge (one as big as my forearm) and due to the apparent lateral bill strikes that were evident when additional bark as stripped several months later:
When it comes to high branch scaling, squirrels can do extensive damage, as in this example on a sugar maple. At the same time, some of the high branch work we’re finding shows clear signs of insect infestation and woodpecker involvement, as in this downed sweet gum limb I found on Saturday. The scaling took place before it fell.
In next example, although the scaling has a little bit of the layered appearance we’ve suggested is more characteristic of Pileateds, it’s clear that woodpeckers are involved, since there are a few places where what we presume to be insect tunnels have been expanded.
While I was initially disappointed by this new data point, not only because it compels me not only to reexamine certain aspects of my hypothesis but also because it eliminates the types of targets we’ve thought most promising in terms of obtaining clear trail cam photos, I recognize that this is part of the process. It’s an opportunity to refine the hypothesis and a reminder to observe carefully. Ultimately, I think there’s more room for confusion between squirrel work and what I take to be IBWO work. We can’t help but wonder whether Tanner himself might have been fooled in some instances.
Frank and a visiting ornithologist spent this past weekend in our search area. I’m eager to read and will be posting Frank’s report before long. For now, suffice it to say they set up three trail cams, one on the snag where we captured the image discussed here and here and one on this downed sweet gum top found in April:
It most likely fell on April 19th. When I found it a couple of days later, it had fresh green leaves attached and no sign of insect infestation. Since then it has been partially scaled. This is an important data point, as we know the scaling took place within five and a half months of death, and Tanner documented the IBWO’s preference for freshly dead wood. We hope there will be a return visit soon.
They also placed a camera on an even more recently fallen water oak, something that started me thinking about possible patterns in the feeding sign we’re finding.
I’ve counted the examples of feeding sign from our current search area I’ve posted on the blog (which is by no means all the suggestive work we’ve found but is generally the most impressive), and the results for sweet gums are interesting, especially in light of Tanner’s observations suggesting an IBWO preference for sweet gums. Our results also suggest a preference for hickory. (Hickories were scarce in the Singer Tract, and apparently the species present in our area were not present there.) In both cases, the frequency with which we’re finding scaling seems to exceed the relative abundance of either type of tree, although we have not made formal counts. This sign was found between the spring of 2012 and the Spring of 2015, except for the downed top pictured above, which was scaled a little later.
The tally includes a couple of examples of work that falls short of what we consider to be diagnostic for IBWO. It also includes the small sweet gum snag that looks like it was attacked with a hatchet.
Edited November 2021 to add: We now have reason to think this is likely Pileated Woodpecker work.
While there seemed to be a preference for sweet gums prior to the 2014-2015 season, the preference was considerably more pronounced this year when the abundance of fresh scaling on sweet gums in a relatively small area was astonishing. Here’s the multi-year breakdown:
Sweet gum: 25
Presumed sweet gum: 6 (One example possibly PIWO)
Oak species: 3
Willow oak: 2
Maple: 1 (Possibly PIWO)
Ivorybills fed on sweet gums in 42.6% of Tanner’s observations, scaling in 40 instances and digging in 3. Sweet gums made up 20.8% of the forest composition in Tanner’s study area. Next on Tanner’s list of preferred foraging trees were Nuttall’s oaks. By contrast, Pileateds “appeared to have no preference for any species of tree.” Tanner observed PIWOs feeding on sweet gums on fourteen occasions; nine involved digging and five involved scaling. He further noted, “What scaling Pileateds were observed to do was mostly on loose bark and was never as extensive or cleanly done as the work of the Ivory-bills.”
On a more speculative note, I think I’ve been able to identify one species of beetle that’s infesting the sweet gums, including the small one shown above. They’re an invasive, the granulate (formerly Asian) ambrosia beetle Xylosandrus crassiuculus (or another closely related invasive). Ambrosia beetles are tiny, but they are gregarious, with adult females creating chambers and tending broods of larvae in the sapwood. They can kill small trees but also infest larger ones. They have a relatively short life-cycle, and one source suggests they can produce 3 or 4 broods a season in the deep south. It’s worth repeating that I’ve seen signs of ambrosia beetle infestation elsewhere in Louisiana (near our old search area and in upland hardwood forest adjacent to our current one) but did not find work suggestive of ivorybills in either place.
We’ve found known IBWO prey species in our search area, on trees that we suspect were fed on by ivorybills. We also suspect that, contrary to Tanner, they may feed on darkling beetles. Could they also be feeding on an invasive species? We can see no reason to suspect otherwise and will continue our investigations with this in mind. I plan to return to Louisiana Thanksgiving week.
I have been re-reading George Lamb’s 1957 report on the Cuban Ivory-billed Woodpecker. A number of items struck me as potentially significant for North American searchers, some for how they diverge from Tanner and others for their level of detail. Since this report is likely unfamiliar to many, I thought I’d do a quick post listing some of the more interesting observations
Lamb references a number of local sightings of “groups” of ivorybills, with one report to John Dennis that involved six birds. Notwithstanding, Lamb estimated the population density in Cuba to be much thinner than in the Singer Tract, at one pair per 12-25 square miles. He also pointed out that “ . . . the Cuban Ivory-bills are living for the most part in a cut-over pine forest where only small and deformed trees remain.”
The Cuban ivorybills fed on pines and hardwoods more or less equally, although most of the feeding sign was found on pines, due to the difficulty of searching for sign in the denser hardwood habitat. Roosts and nests were found exclusively in pines (one unused cavity was found in a hardwood), which is interesting in light of the fact that hardwoods were also available. Cavities were found at heights ranging from under 20 feet to nearly 60 feet. Cavities were higher in mature forest; Lamb suggested but did not conclude that the preference was for higher cavities and that the lower ones reflected an adaptation to cut-over conditions.
Lamb describes a female scaling bark: “At this point she was only about 25 feet away while she was feeding around the base of a small pine. She began ‘barking’ this tree about 30 inches from the ground and slowly worked up to the top.” Dennis too had observed birds scaling small pines. They found more scaling than excavation.
This apparent preference for pines, including small ones, may be significant, particularly since the hardwood areas were “relatively untouched”.
An estimated 17 birds were killed by humans over a ten year period, a huge number for such a small population. And it seems an open question whether the thinner population density noted by the Lambs was due to habitat quality, hunting pressure, or a combination of the two.
Regarding flight style: “. . .the flight of the Cuban Ivory-billed Woodpecker was always level and purposeful. They are strong fliers, capable of covering considerable distance in little time, as indeed they must to live successfully in cut-over woodlands. Although the Ivory-bill did not seem to undulate in its flight, the wing beats were not steady, having an almost imperceptible 2-3-2-3 rhythm.”
There’s no mention of double knocks, but calls are discussed. Lamb describes the sound as like the “note of a penny tin trumpet . . . short and usually repeated in a series of single-double-single beats, or it may begin with a double call: that is a high nasal “pent, pent-pent, pent”, or just “pent-pent”. On several occasions the female Ivory-bill most frequently observed made a few long and very loud calls, soon after leaving here roost tree in the early morning. The notes were of greater duration than normal and were repeated in a series of sixteen to twenty-two kients.”
Food for thought . . .
In this post, I compared scaling on sweet gums in our search area with images of scaling on sweet gums taken by Martjan Lammertink in Congaree National Park; he has graciously granted me permission to post those images and some others here.
The focus of the original post was on the direct comparison between known Pileated Woodpecker scaling on sweet gums and the work we are finding in our search area. The differences are quite dramatic. In this post, I will simply include a number of examples of suspected ivorybill work from both our old and new search areas without too much discussion. The differences should be self-evident, even without reference to bark chips. I have come to believe that much if not all of the high branch scaling that Tanner presented as being typical and (by implication at least) diagnostic is not necessarily inconsistent with PIWO work. Thus, in the absence of other indicators, the Steinhagen photos are potentially interesting but not highly suggestive. Note that in all three images of PIWO work on boles, there is clear evidence that the bark has been removed in layers. This is true even on the pine, where signs of this layered work are visible on the left, just above the bird. I now suspect the absence or near absence of layering on extensively scaled, tight barked hardwoods may be the single most important component in the gestalt and may even be diagnostic in itself.
Even when the scaling is quite extensive, the signs of layering are likely to be a giveaway, as in this example from public land near our old search area. The bark chips around the base of this tree were all small and gave further indication that the work had been done in layers.
Most of the images below have been discussed in other posts. The scaling is on oaks, hickories, and sweet gums and the differences in appearance should be self-evident.