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Red Squirrel Housekeeping

The snow is gone and leaves have not yet filled in the forest canopy, so it’s a great time to look at red squirrel middens. Conifer seeds make up a large percentage of the red squirrel diet, and the animals spend lots of time eating or collecting conifer cones. To get at the seeds a squirrel holds a cone in both front feet and, starting at the bottom, chews off each scale and eats the exposed seeds, spinning the cone as it works its way toward the tip. This is done with typical red squirrel energy, and the scales seem to fly out at blistering speed. The scales and cone cores accumulate around or below the feeding station, and the resulting piles of debris, called middens, can be quite sizable. The mounds in the photo contain mostly the cores and scales of Norway spruce cones. Middens this large must have accumulated over a number of years, probably during the residence of several different animals.

The hole just below the trunk of the closer tree is an entrance to an underground space where cones were stored. These food caches are often located in the spaces around the roots under the middens, but may also be in rock cavities, log piles, or even human structures. They are generally underground where the high humidity prevents the cones from opening.

Red squirrels depend on stored conifer cones for survival over the winter. In late summer and early fall conifer stands resound with the sound of objects hitting the ground as the animals nip the cones in the tree tops. Once a good supply has fallen, the squirrels descend and carry the cones to their underground storage spaces. It’s this habit of creating concentrated supplies in a limited number of locations, called larder hoarding, that allows the animals to inhabit boreal forests with long, snowy winters. Imagine the effort that would be involved if, like gray squirrels, red squirrels had to dig down through a deep snowpack to retrieve each individual food item. With its food stored in larders a red squirrel merely needs to maintain tunnels leading from the surface to the ground-level entrances.

Middens are usually located at the bases of the trees which provided the cones, indicating that the squirrels bring cones up from storage to perches higher in the tree to feed. In the photo above you can see a Norway spruce with several branches (dead but still strong enough to support a squirrel) which could have served as feeding perches. These branches, or ones nearby, are often marked by the squirrels. One such branch is shown in the photo below. The shot was taken from directly above the branch. You can see some partly eaten spruce cones on the ground below in the upper part of the photo, and the dark tree trunk in the lower right-hand area. The branch itself is liberally marked with the fresh gouges of red squirrel incisors, and there are a few older gouges from previous years. The scent compounds left in the wood would establish the resident squirrel’s ownership of that particular real estate.

Middens tell us how much red squirrels depend on conifers for their winter food supply–and it’s not just Norway spruce. Where pines, hemlocks, firs or other spruce species are more common their cones provide the bulk of the winter diet, and similar middens can be found.


In the mixed forests of central New York, middens tell us about the non-coniferous foods that red squirrels also make use of. In the photo above butternut shells with typical red squirrel entry holes are mixed with the spruce scales and cores. I’ve also found the opened shells of walnuts, acorns, and hickory nuts in red squirrel middens. And occasionally a bone fragment, with telltale incisor gouges, sits atop a midden. Red squirrels, like other small mammals, need to boost their calcium intake by chewing on bones, and a familiar feeding perch makes a fine location for a dose of minerals.

Spring Fever among Woodchucks

If you think you have it bad, just consider the woodchuck. The males emerged from hibernation weeks ago only to find the ground covered with snow. There wasn’t much to eat, and the weather wasn’t very spring-like. But no matter–they were more interested in procreation than food or comfort, and they spent their time searching out burrows occupied by females. Upon finding a receptive female the male entered the den and copulated with her, then moved on in search of another one. With nothing much to eat the roaming males, which may have dropped up to 1/3 of their body weight during hibernation, lost even more body mass. Meanwhile, the female woodchucks remained underground and got a few more weeks of sleep.

This delayed emergence is important because, like the males, female woodchucks have already lost weight during hibernation and losing even more would impair their ability to give birth to healthy young. Their appearance above ground coincides with the onset of new spring growth and their condition improves rapidly.

I found the den pictured below in early March. A few inches of new snow covered about a foot of denser old snow, which made for nice tracking. There weren’t any tracks beyond those shown in the photo, so it looked like the animal came out, took a look around, and then went back into the burrow. The mud-on-snow tracks are remarkably clear–check out the right front print just to the right of center.

Finding such unmarred tracks around burrows becomes less likely as the season advances and the animals make more forays to and from their winter refuges. The photo below, also from early March but taken a few years ago, shows the muddy and partially melted evidence of several trips. In both of these cases the weather was still pretty cold and there was a substantial snowpack, so these were most likely males in the throes of spring (or rather mating) fever.

As winter loosens its grip woodchuck tracks start becoming more widespread in fields and forest edges. In the photo below the direction of travel is from the lower left of the frame to the upper right, and the impressions form a zig-zag pattern. Each angle of the zig-zag is composed of two


tracks, the rear positioned roughly on top of or close to the front track from the same side. These are the characteristics of the indirect register walk, the woodchuck’s most common gait. Starting from the lower left, the sequence in the photo above is right hind on right front, left hind on left front, right front with right hind just ahead, left hind on left front. To the right of the first set of left front and hind there are some gray squirrel tracks heading in the opposite direction.

By the way, woodchucks are also known as groundhogs, but I prefer the name woodchuck, because the word derives from one of its Native American names. Woodchucks weren’t as common in pre-colonial times as they are now, but their populations would have been concentrated around cultivated fields so they would have been familiar to Native Americans. They still thrive in agricultural landscapes, and are sometimes seen as pests. From an ecological point of view they are actually beneficial. Woodchuck excavations help to turn over and aerate soils, and their burrows provide homes for many other animals.

The photo above shows a burrow I found after a very cold night. Rabbit tracks led both in and out, but this hole wasn’t dug by a rabbit. Unlike European rabbits, which construct extensive tunnel systems called warrens, our cottontails don’t dig burrows. They get along just fine without underground housing, unless it’s very cold. When that happens they find shelter, and that shelter is often a woodchuck burrow.

An Encounter with a Fisher

Sightings of wild mammals are generally rare, and when they do occur it’s usually just a quick glimpse of the tail end of the animal as it flees at top speed. So my recent encounter with a fisher was doubly unusual. I was walking downhill on a sloping section of forest road (Hammond Hill Road in Hammond Hill State Forest for those who know the area). That part of the road is straight so I could see pretty far down the hill, and I suddenly realized there was a dark animal moving around on the road far below. I froze, not sure at first what kind of animal it was and hoping it wouldn’t realize I was there. It didn’t–in fact it actually began coming up the hill toward me. As I got a better view of its elongated body, short legs, and long fluffy tail I realized it was a fisher. I watched as it moved in a completely relaxed manner–apparently unaware of my presence–and marveled at its beauty. I was afraid if I made a move to get out my camera the fisher would take off, so I didn’t dare try for a photo. But here’s a good photograph of a fisher obtained from the Vermont Center for Ecostudies (https://vtecostudies.org/blog/walk-with-the-fisher-on-outdoor-radio/).

Photo courtesy of the Vermont Center forEcostudies

The fisher continued to move uphill in my direction at a steady bounding gait, with an occasional pause to look around. When less than 50 feet separated us, it suddenly realized I was there. It stood up on its hind legs, stared at me for a few seconds, and then bounded off into the trees.

Of course I immediately went to look at the tracks. Because the snow was dry and fluffy most of the prints weren’t clearly defined, and the cloudy conditions made things even harder to see–and nearly impossible to photograph. But there was a spot farther down the hill where the snow was firmer and the track details showed up better. A set of four prints from that part of the trail is shown in the photo below (direction of travel from right to left). The pattern

Track sequence, starting from the right: right front, left front, right rear, left rear.

resembles the bound of a cottontail rabbit: the two front tracks are narrowly set behind the rear tracks, and one (the left front) leads the other. The rear tracks are more widely separated and almost even with each other. Typical mustelid structure shows in the prints: the five toes are arranged in a lopsided crescent and the middle pads form a smaller crescent behind the toes.

That was only one of several different gait patterns I saw as I backtracked along the fisher’s trail. In true mustelid fashion the animal had been very flexible in the way it placed its feet. Rather than showing the rather poor photos from that day I’ll illustrate two of the variations I saw with shots that I took on other days (the direction of travel again is from right to left). As in the opening shot the four tracks in the photo below are well separated, but the rear prints are staggered rather than even with each other, and one is positioned slightly behind the leading front print.

Track sequence, starting from the right: right front, right rear, left front, left rear.

In the next shot the left rear foot came down on top of the left front, leaving a pattern that looks at first like there are only three tracks. But in the heel area of the middle impression there’s an inner ridge and a wider area of disturbance to its left, showing that two feet did actually land there.

Track sequence, starting from the right: right front, left rear on top of left front, right rear.


In addition to those two there were other variations–changes in the leading front or rear foot and slightly different placements of the second and third feet to hit the ground–but to my eyes the fisher’s bounding movement appeared to be uniform and unvarying. Except for momentary pauses it moved steadily uphill with the gently arching leaps that are so typically mustelid. One difference did stand out, and that was a variation in the leap lengths: the four-print patterns that matched the one shown in the first photo were separated by slightly longer distances than the patterns shown in the second and third photos. The fisher apparently wanted to move faster, and I suspect that the more even placement of the rear feet in the first photo delivered more power and enabled longer leaps. But there were many variations in the patterns that didn’t involve any changes in leap length, so there must be other factors that cause a fisher to vary the way it places its feet. I can only imagine the subtle interactions that go on between the animal and its surroundings. I hope that with further study of fisher trails, and maybe even some additional encounters with fishers, I’ll be able to understand more of the puzzle.

The Allure of Scent Marking

Deep in the coldest months of winter, when you’d think every animal is single-mindedly focused on survival, some predators are being distracted by an equally compelling urge–mating. Even as the snow flies, time spent hunting decreases and behaviors connected with reproduction become more predominant. For the tracker one of the best signs of this change is an increase in scent marking. I followed a red fox trail recently, and she was detouring to urinate on raised features like this stump every 500 feet or

so. I say she because the arrangement of tracks and the placement of the urine could only have been done by a female fox. In the photo the small spots in the left half of the stump are urine (you can ignore the dark chunk of bark near the center). The fox came in from the lower left, paused on the upper side of the stump to pee, and proceeded towards the upper right. The more deeply impressed track marked SF was made by the supporting rear foot (the left) while the right rear was raised. During mating season red fox urine has a strong, slightly skunky–but not unpleasant–odor that is obvious even to us smell-challenged humans. So as I followed the trail the air was perfumed with fox musk.

My dog Banjo (dogs are great teachers for wild canine behaviors) demonstrates the technique in the photo below, supporting her weight on her right rear foot plus the two front feet and positioning her left rear leg up and forward. You can actually see the urine squirting downward under her rear end.

Male canines also raise a rear leg when they urinate, but the leg is held out and back, and the urine goes out to the side rather than downward. I don’t currently have a male dog so I can’t show you that, but I’m sure you can imagine the posture. A male coyote, traveling from left to right,

made the scent mark above, supporting its weight on the right rear foot (the track at the lower center) and shooting the urine sideways onto the upper part of the stump. Coyote urine has a mild odor and isn’t nearly as detectable by humans as fox urine is.

Bobcats also feel the mating urge in the winter, and again, those who have house cats, especially males, may have observed the technique. A male bobcat left its signature on the log in the photo below, coming in from the top of the frame, depositing its message, and leaving at the lower left.

It first gave the log a good sniff (revealed by the front print facing the log), then turned so its rear was facing the wood and sprayed urine backwards. Here’s the photo again with the tracks marked.

S denotes where the bobcat placed a front foot as it sniffed the log. RH, LH, RF and LF show the four feet in a squared posture as the cat faced away from the log and urinated backwards. Bobcat urine, like house cat urine, has a strong odor of ammonia, so if you had been there to sniff the side of the log you would have detected the cat-box odor. Female bobcats also scent mark, mostly downward from a squatting position.

Scent marking by wild canids and felids continues through pair formation, den preparation, and birthing. Soon after that hunting begins to regain its importance as the pressure to provide food for the growing young increases. But the timing of reproduction isn’t accidental. The earlier onset of predator reproduction means that their greatest need for food coincides with the greatest abundance of prey animals, which mostly mated in early spring and multiply during spring and summer.

The Ups and Downs of Snowshoe Hares

Snowshoe hares are having a banner year. In early December I spent some time in the western Adirondacks, and it seemed like there were snowshoe hare trails everywhere. A bounding hare-like its cousin the cottontail rabbit-typically leaves sets of four prints in Y shaped arrangements. The two larger rear prints are usually even with each other and widely spaced while the smaller front prints are behind the rear, staggered,  and placed along the center line of the trail. 

In the photo at the right (direction of travel from right to left) the hind tracks are the larger and somewhat triangular prints on the left side. The right front print is near the center of the photo and the left front print is behind it toward the right edge of the frame.

The hare that made the tracks above didn’t sink very far into the snow, so it’s easy to see all four prints. But when temperatures stay low and the snow keeps falling there may be a foot or more of light, fluffy stuff on top that doesn’t offer much support. That’s the way it was during my recent Adirondack visit. Even the snowshoe hares were sinking deeply at every leap, and their landing patterns didn’t look the same.

In the photo at the left a bounding hare traveled from bottom to top, leaving a triangular hole each time it landed. At each landing the front feet plunged into the snow at the narrow lower part of the triangle. The more widely held hind feet–each foot spread out laterally for maximum support–landed just past the front feet to form the wide upper part of the triangle. The width at the widest part of these craters can approach twelve inches.

Snowshoe hares, like cottontails, tend to use the same travel routes repeatedly. This creates trails that offer firmer footing and easier movement, like the one shown at the left. I’ve read that these trails help the hares escape from predators, but I’m not sure about that. Maybe the predators can move more easily as well.

Snowshoe hare populations are known to go through cycles of abundance and scarcity. These cycles are especially pronounced in the Boreal forests of Canada, where population numbers of the Canada lynx are closely tied to the abundance of hares. The Adirondacks host a greater variety of both predators and prey–although there are no lynx–and population fluctuations don’t reach the same extremes for either prey or predators. But when hares are more abundant than usual, as they seem to be in the western Adirondacks this winter, young fishers, coyotes, and bobcats–the main predators of snowshoe hares in this region–are more likely to make it through their first winter. I hope to visit the same locations over the next few months, and I’ll be paying special attention to the tracks and signs of all the animals in the web of relationships that includes the snowshoe hare.

Lessons from Flying Squirrels

The weather has been unusually cold and snowy for early November, and there have been days when conditions were perfect for seeing detail in the tracks of small animals–an icy base with about half an inch of new, soft snow on top. On one of those days I went to a location where I had seen flying squirrel trails in past years, and I found some beautifully detailed prints. In the photo on the right (direction of travel to the right), the right rear track is at the bottom of the frame, and the right front is just above it. The other two prints are at the top, the left rear just behind the left front. The toes  and middle pads show up nicely in both front and rear tracks. The heels of the rear prints made impressions, and the paired heel pads of the right front track  can also be seen.

Now compare the shot above with these chipmunk tracks, photographed on the same day and arranged almost identically except that the left front track is just below the left rear. There’s a similar amount of detail, with toes and middle pads clearly visible in both front and rear feet and the paired heel pads showing in both front feet. I had hoped that if I found really detailed tracks I would see features that would separate chipmunks and southern flying squirrels, but to my eyes there are no appreciable differences between the tracks in the two photos. The dimensions are similar as well: both sets of prints have a trail width (the distance from the right edge of the right rear print to the left edge of the left rear print) of 2 inches, and the length of the front track is 9/16 inch for the flying squirrel and 5/8 inch for the chipmunk, not significantly different. So how did I know that the tracks in the first photo were made by a southern flying squirrel, while those in the second belonged to a chipmunk?

The answer came from the differing trail patterns. Southern flying squirrels have flaps of skin (patagia) that connect the front and rear legs all the way out to the ankles, so they move differently from chipmunks (and also from tree squirrels, for that matter). The front tracks of a bounding southern flying squirrel are set almost as wide as the rear, and they are usually in front of, or occasionally between, the rear tracks. Because of the skin flaps, flying squirrels are not as fleet-footed on the ground as other small rodents, so their leaps are shorter. Compare the southern flying squirrel bounding trail in the photo above (traveling from bottom to top) with the next photo of a trail made by a chipmunk (traveling from top to bottom). In its normal traveling bound the chipmunk consistently places its rear feet ahead of its front, and its leaps can be much longer than those of the flying squirrel. Of course chipmunks do sometimes make short leaps, and they do sometimes place their front feet between (as in the second photo of the blog) or ahead of the rear. That kind of pattern in a chipmunk trail is an indication of a break in the rhythm, while it falls withing the normal bounding pattern for a southern flying squirrel. (By the way, neither of the bounding photos came from the day I took the close-up shots, but they illustrate the trail patterns I saw that day.)

More snow changes everything. All bounding animals switch to what I call a double-register bound when their feet sink deeply into the snow. The trail pattern consists of sets of two impressions more or less side-by-side, created when the rear feet come down in the holes just made by the front feet. For an animal the size of a flying squirrel even a few inches of soft snow can be enough to change its gait pattern from its normal bound to a double-register bound like the one in the photo at the right (direction of travel from lower right to upper left). The relative positions of front and hind prints no longer apply, but trail width can still be measured, and this trail had a trail width of 2 1/8 inches, squarely in the range for the southern flying squirrel. A chipmunk trail would have had a similar trail width, but the trail pictured above was made during a long stretch of cold weather. Chipmunks wait out winter’s coldest periods in a state of torpor in their underground refuges, while flying squirrels come out regularly even in frigid temperatures.

Squirrels Share Some Secrets

I’ve been getting more and more interested in squirrels. Like all animals, their lives are shaped by the seasons, and there’s much to discover if you can find and decipher the signs they leave. In late summer squirrels bite off oak twigs to get at the ripening acorns, and the “nip twigs”  (minus acorns) can be found scattered under oak trees. The acorn remnants–shell fragments and partly eaten acorn meats–may also be found on the ground or on nearby logs or stumps where a squirrel has a good view of its surroundings while feeding.

In September I found these apparently uneaten acorns, along with cap and shell fragments, scattered on the ground beneath some red oak trees. The acorns were intact, but every one was marred by brown spots. This puzzled me at first, so I got out my magnifier and took a closer look. I noticed that there were tiny tunnels in some of the brown spots, and one even had a minute, worm-like insect larvae. I also saw indistinct gouges in a few of the brown spots that looked a lot like tooth marks. Mystery solved! The squirrels were feeding on acorn weevils, often found inside acorns and much richer in calories than the acorns themselves.

We’ve had a very wet fall, and fungi have been popping up everywhere. I’ve been surprised to see how fond squirrels are of mushrooms. I’ve repeatedly come across mushrooms which had been plucked from where they had grown, carried to some other spot, and partly or almost completely eaten. Bite marks sometimes showed along the edges, and there were always discarded pieces scattered around–squirrels seem to be sloppy eaters. Slugs and snails also seem to love mushrooms, but they simply make broad, shallow gouges in the caps and the mushrooms remain standing where they grew.

When the weather turns colder squirrels give up their summer leaf nests and move into more sheltered lodgings, often in hollow trees. Instead of using leaves, they line their nests with fibrous material. The inner bark of this dead branch was stripped off by a squirrel and used to provide warm insulation for its nest. The smoothly denuded wood surfaces and hanging remnants are typical of squirrel work. In addition, there are usually a few gouges made by the animal’s incisors somewhere in the debarked area. Dead branches are the most common source of good nest lining material, but the bark of living honeysuckle and other shrubs is a favorite material where they are available.

You may have been wondering which squirrels I’ve been talking about. Actually, I’ve purposely avoided naming them because I’m often not sure. Our mixed forests host both red and gray squirrels, not to mention northern and southern flying squirrels, and it’s often difficult to know which species left a particular sign. I suspect that the oak nip twigs and the weevil feeding were done by gray squirrels, but red squirrels also feed on acorns. I’m pretty sure both red and gray squirrels eat mushrooms, and all of our squirrels line their winter nests with fibrous material. There are some types of sign–certain kinds of marking, and large middens under conifers–that can definitely be attributed to a particular species; more about those in future blogs. Until then, we’ll adopt the wise tracker’s attitude and recognize the limits of our certainty.

Busy Bears

I just spent a wonderful week in the western Adirondacks, and I was able to indulge in one of my favorite activities: exploring the Independence River on foot–in other words, wading. Besides being breathtakingly beautiful, the Independence is small enough to be safely waded when water levels are low, and there are plenty of sandbars and silty edges where tracks can be found. These bear tracks were the find of the day. The bear was traveling from left to right, and my dog (she likes to explore rivers with me) left tracks below the bear’s,  going in the opposite direction. The first bear print at the upper left is the right front, and just to its right is the right rear. A little farther to the right is the left front print and to its left the left rear. The pattern of rear print ahead of front from the same side tells me that the bear was moving at an overstep walk–a gait often used for relaxed investigation or leisurely travel.

I was excited to find bear tracks because they’re not always easy to find, especially in late summer when the animals are spending much of their time in forests, overgrown clearings, or other relatively untrackable places. The bear may have visited the river to drink, or perhaps to use the shoreline as an easy travel route to a new food source. But even if there are no tracks to be found, there are usually plenty of other indicators that bears are in the neighborhood. Bears use a variety of marking techniques to communicate with other bears, and these marks are often prominent and long-lasting. A bear raked this white pine tree with its claws, leaving fresh claw marks which oozed with copious sap flows.

Man-made structures like signs and lean-tos are often targets of bear marking. On a different day during my recent visit to the ‘Daks I walked along a forest road where posts had been set to mark the locations of culverts. It was clear that bears were habitually using that road–many of the posts, like this one, were ravaged by bear bites. The brighter wood exposed by the bites stands out to our eyes, but for the bear the scent of the saliva-soaked wood is probably more important.

Teeth and claws aren’t the only things bears use to make their presence known. They often rub against trees or wooden structures leaving a personal scent signature from the oils and sebaceous chemicals in their fur. Another post along that same forest road was decorated with hairs left by a bear that had done just that.

And then there’s always scat. Piles of bear scat provide long-lasting samples of what bears are eating. This time of year in the Adirondacks black cherries are a favorite item, as demonstrated by this example. Elsewhere the skins and seeds of apples, grapes, viburnums and berries; squash and pumpkin seeds; corn kernels; or the shells of hickory nuts, beechnuts and acorns may show up in late summer scat. This is the season of ursine hyperphagia, the insatiable hunger that drives bears to eat almost 24 hours a day. The thick layers of fat they put on will allow them to survive their long winter hibernation.

Feet Tell the Story: Family Resemblances Among Small Rodents

The smaller the creature, the tinier the feet–and the less often we’re able to see the kind of detail that we’re accustomed to seeing in the tracks of larger creatures. So I was delighted a few weeks ago to find these beautifully revealing chipmunk tracks. The one that first caught my eye was the right rear print that lies off by itself in the lower right part of the photo. The much larger rear print of a gray squirrel lies above it, and at least two other chipmunk tracks are visible among the unrelated disturbances in the upper part of the photo. The chipmunk’s right front print sits in the left part of the frame midway between top and bottom, and its left rear print can be seen above the squirrel track. The left front print isn’t obvious but a few small depressions suggest that it lies above the right front in the upper left quadrant of the photo. The chipmunk was moving toward the right.

The two right prints of the chipmunk show excellent detail, so I’ve focused in on them in the photo to the left. The toes and claw marks are visible, four of each in the front track (at the upper left) and five in the rear track (at the lower right). Behind the toes you can see the grouped depressions that make up the middle pads of both the front and rear tracks. For such a small creature those tracks are exquisite.

Why do I get so excited about such stuff? The finely formed details of animal tracks contain such energy and elegance that I just love to look at them. But beyond that, track details can reveal an animal’s affinities, in this case the affinities between chipmunks and other small rodents. The gray squirrel tracks in the next photo (moving toward the top of the frame, rear prints above and front prints below) help to illustrate the important features shared by this group. In the rear prints the central three toes lie close together and point forward, while the inner and outer ones sit farther back and are angled to the sides. The four toes of the front prints are spread more or less evenly. The middle pads of both front and rear feet are made up of four depressions, arranged in a crescent in the rear and a more triangular shape in the front. In the front print the heel pads, located just behind the middle pads, show as small paired depressions.

There are lots of rodents, and some have foot structures that depart from the characteristics I just described. But our most common small rodents–including one even smaller than a chipmunk–are surprisingly consistent in showing this suite of features. It took perfect mud to register the details in these white-footed mouse tracks (heading toward the top of the photo), but the family resemblance comes through clearly. The numbers and arrangements of the toes are the same, and the middle pads of both front and rear prints are similar to those of the chipmunk and the squirrel. You can even see the heel pads, albeit slightly smeared, in the front tracks!

Family resemblances can extend to the gait level as well, and they certainly do here. Widely placed rear prints and more narrowly placed front prints, positioned behind the rear ones, represent a typical pattern for bounding or jumping small rodents. Of course this pattern changes when different maneuvers are required, and even at a steady bound the four tracks aren’t usually as perfectly placed as the ones in the snow photo of the gray squirrel. But both gait patterns and track details are useful clues to the identities of our most common small rodents.

Crossing Paths with the Red Fox

Summer tracking doesn’t often involve those infinitely unfolding trails of winter in which we see extended (to us) segments of the daily lives of animals. Without snow we’re more likely to encounter evidence that reveals the presence of a creature in a particular spot for a mere instant. But I treasure these discoveries just as much, and I find them to be equally valuable as learning opportunities. Imagine you’re out on a pleasant summer hike, and you come to the muddy patch shown in the photo. It’s busy with the tracks of mountain bikes, dogs, and people’s boots, and you’re tempted to simply step around the mess and continue on. But instead you push yourself to look more closely, and you immediately notice a couple of intriguing prints (located just to the right of center in the photo). As you examine them you see that they are the rear (above) and front (below) tracks of a canine, and they surely don’t look like domestic dog. The lower print, shown in the next photo (it’s located down and to the right of center in the first photo), exhibits plenty of revealing detail. The toes are held tightly together, with the outer and inner ones tucked closely behind the two leading toes. There is a nice canine X made by the ridges between the middle pad, the inner and outer toes, and the two leading toes pressed together. The mud is textured by compressed hair, and a chevron-shaped indentation shows in the middle pad. Claw marks are faint except for that of the left leading toe, which is slender and points straight ahead. This is unmistakably the front print of a red fox, and the smaller print ahead and to its left is a rear. Other than those two tracks the fox left little evidence of its passing, but I was delighted to know that it had traveled the same trail I was following.

The hairy feet of the red fox feet set it apart from any of our other wild canines, and the hair sometimes shows beautifully in the fine silt and mud of summer. Here’s a photo from a muddy spot along an ATV trail in which the hair is really obvious. The front track is at the upper right and the rear is at the lower left. (Between them is the track of a raccoon that was turning to the left.) In addition to the hairiness, you can see the difference in size between front and rear tracks as well as the bar in the middle pad of the front print.

These red fox prints turned up along a forest road in a spot that funneled animal movement across a stretch of perfectly moist mud. In the photo you can see a front print in the upper right corner (there’s a maple seed partly covering two toes) and behind that print a rear track, both heading toward the right. In the lower left quadrant are a front and rear that are going in the opposite direction. What I love about these tracks are the peculiar indentations where the surface layer of mud was actually picked up by protruding parts. Take a look at the front track in the upper right corner. The chevron in the middle pad picked up the surface layer of mud and left a slightly curved indentation. The small horny pads that sit at the tips of the toes and protrude from the hair also picked up some mud and left oblong indentations. And the same thing happened in the two leading toes of the rear print (over to the left of the front print) to produce oval indentations. Around some of these holes there are larger shadowy impressions that show where the rest of the toe touched the mud. The hairless protruding parts of red fox feet don’t always show in tracks, and you may wonder, as I have, whether they serve any purpose.

Purely by coincidence we’ve progressed through stages of muddiness from deep and soft through more resistant but still wet to firm with a moist surface layer. So to finish that sequence here’s a print from mud that was almost unyielding and nearly dry. Again it’s a red fox print, but a very different looking one. (The card at the upper left is a one inch square for size reference.) The direction of travel is toward the right, and the deepest marks were made by the claws punching into the mud. The tips of the horny toe pads (the same structures that picked up bits of mud in the previous photo) show behind each claw mark, and in the area of the middle pad we see the chevron. If the fox had been moving slowly we would have strained to detect any evidence of its passing, but this fox was going fast enough for the claws, the small protruding toe pads, and the hairless chevron of the middle pad to push into the hard mud. And here’s a possible answer to our question from the preceding paragraph. These structures must have helped to give the fox traction. Perhaps without them the hairy feet would slip and the fox’s footing would be compromised.