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Determining Direction of Travel on a Fisher Trail

“Which way them critters goin’?” my friend Dani would call out every time I mentioned I was leaving the house to go tracking, and to this day it can be really tricky, especially in deep snow. For me it takes a good amount of analysis from the moment we encounter a trail, and all throughout as many animals will backtrack, circle round, walk on older trails, walk in another animals trail, or even in their own older trails. There are many points when trailing an animal that the direction of travel can be confused or undetectable entirely. But instead of giving up, we have processes that can help us, especially when they are used in combination over longer stretches of the trail.

For this exploration in determining the direction of travel (DOT), I’ll use a snowed in Fisher (Pekania pennanti) trail we encountered during an Earth Tracks Tracking Apprenticeship outing at Bognor Marsh, near Meaford, Ontario as an example. It was a faint trail, mostly snowed in, but the impressions were visible at the right angles, as long as they hadn’t been blown away in the wind.

Shape and angle of the impression

Rounded solid edge would indicate the direction of travel (DOT).

It is certainly hard to see in the photos, and believe me when I write that it was also hard to see in person. At some spots these tracks were invisible to see entirely, and some you had to look at the trail in just the right angles to see the faint snowed in trail. But we took the time as we wanted to fore track the Fisher, to follow them in the direction they were going in, rather than back track and go in the direction which they had been coming from.

When we first came up to the Fisher trail we quickly examined the faint impressions to look for the shape of the impressions. I wanted to see if there was a broader rounded edge and a narrower tapering edge of each track. The broader, more solid edge of the track would be where the toes are, and this edge tends to be deeper than the heel or back of the track, as I have noticed that most wild animals tend to be a bit more “toe heavy” and their feet sink in at the front a bit more. The heels however do not always register in the track as deeply and tend to taper in appearance and depth. So in the photograph above and the poorly drawn image on the right would both indicate that the Fisher’s DOT is towards the top of the screen.

Look for the toes

Even though we didn’t find any clear tracks on this particular trail, looking for impressions of the toes at the front of the track is very useful technique for discerning the DOT. Deep incisions into deep snow are often angled in such a way that we can’t see the track floor where the actual imprint sits. We can still use this track to determine the DOT by digging away a few layers of snow, or taking off our gloves and using our bare hands to feel the track. By doing this you can sometimes feel the number of toes, or the ridges between the toes like the cleave between toes 3 and 4 of a deer.

Behaviour like turns and stops + Look for the track pattern

As we carried on the Fisher trail we encountered a couple of times where the Fisher slowed down and investigated. We couldn’t tell what the Fisher was concerned with but we could tell that they slowed and turned. One way we could tell this was by looking at the track pattern left in the snow. In the photo above, the Fisher slowed to a walking gait as they made their way up from the bottom right of the image. Then their trail arced back towards the bottom left of the photo before quickly continuing on their trail in a loping gait towards the top of the image, leaving behind quicker 3×4 and 4×4 track patterns.
We can look at the track patterns and consider the movements of the animal by comparing with what we know about Mustelids (the Weasel family to which Fishers belong) and by thinking of ourselves. Weasels and humans tend to slow down when when investigating something. We will walk to look carefully, and only when we are ready to move on will we jump back into high gear and take off again. This change of gait, from a slow exploratory walk to a faster 3×4 loping gait used by Fishers to cover ground, can be seen as an additional tell of the DOT in the trail. So once we see the DOT we can recognize that the track patterns left behind indicate that the animal moving from the bottom of the image, across and arcing to the left, then up the image and out of the frame.

If we were to imagine the Fisher or ourselves coming from the opposite direction, from the top of the image down towards the bottom, we could see that the animal is moving quickly because of the track pattern indicating a faster gait. They then stop suddenly, without an apparent disturbance to the snow, leaving no slide from slipping, no thrown debris from the forward momentum. The trail would then have to be interpreted as the Fisher walking steadily backwards in an arcing trail until out of the frame on the lower right. While I have seen a Mink (Neogale vison) walking backwards to avoid being noticed, this behaviour is pretty rare and unlikely. Instead we have to assume the more likely storyline, while putting the pieces together in a logical way, noting the behaviour of the Fisher. If we do this we can see that their DOT was towards the top of the image.

Pointing with feet

Pointing with feet implies the times when an animal is looking in a specific direction, perhaps to see what is going on, or to listen, or perhaps even to browse on some nearby shrub. The animal will put out a front foot in the direction that they are looking. The track may be very lightly impressed in the snow. The track will appear out of baseline, out of the regular rhythm of the regular track pattern left behind, indicating that something happened here and it is worth checking out. This is also a moment to determine the DOT because the front foot, either left or right, will be facing forwards towards the DOT but perhaps slightly to the side.

I see this a lot with ungulates such as White-tailed Deer (Odocoileus virginanus) and Moose (Alces alces), but have also see this with Lynx (Lynx canadensis) and Coyotes (Canis latrans). I realized I didn’t get any photos of this behaviour, but it could be lumped with the heading above.

Debris

As mentioned above, another good way to determine DOT is to look for debris in the trail, especially snow kicked up at the front of a track. I was discussing this characteristic with a student this Winter who was quick to demonstrate that snow will be pushed out of a track to their rear, pushed behind them as they lift their foot as result of forward propulsion. They then replicated this by sticking their boot into the snow in a mock step and then intentionally dragging snow out behind them. My response was to point something out ahead of them, something too small to see from where they were standing. They had to walk over to the fictional point of interest, now distracted from the point they were trying to make. When they have walked over to take a look, distracted from the point they had just made, I got them to stop, turn around and look at their trail. Most of the snow had piled at the front of their tracks where they lifted their boots out of the snow. This was pretty convincing.

Now, snow or other substrates can be thrown back behind a track when an animal, including humans, are moving at a faster pace, pushing off of the ground with a forceful step, but I only remember seeing this when someone is starting to move in a run. When I think of it now, it makes me want to go out and try some experiments with a tracking class and see what we can figure out. Will more snow be thrown backwards as more force is being used to propel a body forward?

“When in doubt, track it out”

Once, we were on a Red Fox (Vulpes vulpes) trail for four hours before seeing a sign of the DOT. The snow was too deep to see toes in the tracks, and when we reached in, we still couldn’t make it out. We followed the trail for the morning and then stopped for lunch. It was only after lunch that we encountered a stretch of the trail where the fox had jumped over a log, knocking over some snow which had piled up on the log, that we were able to tell which way the fox was going. We looked to the snow to tell which way it had been knocked over to determine the DOT.

I share this story because sometimes it’s truly difficult to figure out the direction of travel. I have been challenged over and over, humbled so many times by different animals moving through varied substrates at multiple angles of slope. It really comes down to taking our time to sort it out with each new trail we encounter. We can use the tools described above, and likely many more I don’t know about yet, but this takes time in the field and patience with the trail.

“When in doubt, track it out.” Persist in the journey. Focus on the baseline and any changes in the track patterns which may indicate behaviours, and then feel out those behaviours to see if it feels like it would fit the mechanics of the animals body. Look for the deepest part of the track and for debris kicked up at the front of the track. And if you still can’t sort it out, keep going.

To learn more :
Mammal Tracks and Sign by Mark Elbroch and Casey McFarland. Stackpole Books, 2019.
When the Snow Gets Deep – blog post by Linda J. Spielman

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White-tailed Deer feeding sign at Kinghurst

Recently, at a TCNA “tracker tuesday” call, there was a challenge proposed: on your next tracking outing, practice following the deer or the rabbits and see if you can find 10 plants which they fed on. For me in my area, the deer would be White-tailed Deer (Odocoileus virginianus) and the rabbits would be Eastern Cottontails (Sylvilagus floridanus). While I have been observing the Cottontails loosely at work with my students, for this tracking outing with the Earth Tracks Wildlife Tracking Apprenticeship, we focused on the White-tails.

Winter food finding in Southern Ontario is tough for all species. Not only is there a lot of snow on the ground, many of the common forbs which the Deer consume are long dead and the remaining and accessible plants are mostly tougher woodier species which tend to be harder on the teeth and harder to digest. In addition to these impediments White-tailed Deer prefer a mixed bag of food sources. They tend to seek out a variety of mixed forage. While occupying smaller “yards” or Winter territories the White-tails often have less diversity of choice. While their Spring, Summer, and Fall diets are of a more cosmopolitan variety, in Winter they are forced to live off less.

It’s important to consider not only what the deer are eating, but also how. Let’s remember the basics. White-tailed Deer bite off the ends of twigs with their incisors, the teeth at the very front of the mouth. We may think of our own incisors at the top and bottom in the front of our mouths, but when it comes to the Deer they only have incisors on the bottom mandibles. This is also true for a few other species as well, such as everyone else in the family Cervidae (including deer, Moose, Caribou, Reindeer), members of the families Giraffidae (Giraffes, etc), and the family Bovidae (Cows, goats, sheep, etc). All members of these families have no incisors in the cranium. Instead, when they bite those twig ends off they rip them off by grasping the twig end between their lower incisors and the hard palate above. Some other species, such as members of the Rodentia and Lagomorpha orders, cleanly slice twig ends off, but for these no-upper-incisor-having species, it’s often a ragged rough hewn rip. See if you can see this in the photos below.

In “Deer (The Wildlife Series, Book 3)” (Stackpole Books, 1995), Dietland Muller-Schwarze wrote that Deer, like other ungulates, have quite a lot of circumvallate papillae (one type of many bumpy structures on the tongue that gives it the rough texture). In Humans (Homo sapiens), we have between 8-12 of these large structures near the back of our tongue and each structure holds about 100 taste buds. These taste buds on the circumvallate papillae are especially sensitive to bitter tastes. Muller-Schwarze writes about how Deer will commonly spit out bitter forage when they come across it, but for me, this begs the question of how bitter is too bitter for a Deer? Some of the plants described above and below can be pretty bitter tasting to me but I am curious about the time of year when bitterness is most expressed in a plant? I think of bitter annuals in early Spring like some of the Mints (Lamiaceae) and Mustards (Brassicaceae), how often to the Deer munch on these? Perhaps we’ll need to keep an eye out in the Spring to find out.

Lucky for the Deer at Kinghurst, there is a variety of fine forage for them in the Winter. Here I will share some of the variety of plants which we observed feeding sign on, listed in the order in which we came across them. I would love to trail the deer in other areas in Southern Ontario and see what they forage on there. Next time..

 

 

1) Alternate-leaved Dogwood (Cornus alternifolia)

The Alternate-leaved Dogwood is also known as Green Osier and Pagoda Dogwood. I think Pergola would be a better name as a pagoda is multistoried and closed on the sides, while a pergola is single storied, and open, more closely resembling the growth form of this outlier in the Cornus genera. I write outlier because the Alternate-leaved Dogwood is just that, alternately leaved and branched, while the rest of the Cornus are opposite branched or whorled. White-tailed Deer tend to consume both the leaves and the twigs.
C. alternifolia is plentiful at Kinghurst. They tend to grow as an understory shrub in open woods, ravine slopes and hillsides, in forests with mature canopy species such as Sugar Maple, Eastern Hemlock (Tsuga canadensis), and Yellow Birch (Betula alleghaniensis). There are the places where the White-tail tend to hang out.

 

 

2) White Ash (Fraxinus americana)

Common species in the upland forested landscape which I tend to see coming up quickly in areas where other coniferous trees have come down, leaving a gap in the canopy. Most of the larger White Ash and Black Ash (Fraxinus nigra) we found were riddled with Emerald Ash Borer (Agrilus planipennis or EAB) sign and epicormic shoots, but the younger ones the deer were hitting, not so much. We did find one massive old White Ash with a Winter Porcupine (Erethizon dorsatum) den in the base, with the Porcupine huddled up inside. I did not see any sign of EAB on this big one and wonder if they are resistant somehow? If this individual tree is resistant somehow, I hope they are a pistilate or seed flower bearing individual (White Ash trees are either pollen flower bearers or seed flower bearers) and survive to spread viable seed with that same possible EAB resistance. We noticed lots of feeding sign adjacent to the den, but this was Porky sign with 45°ish cuts at the end rather than the ragged cuts the deer tended to leave behind.

 

 

3) Eastern White Cedar (Thuja occidentalis)

Eastern White Cedar is the one of the most important food plant in the Northern woods; one of the only green plants in the NorthEast which can sustain deer in the critical part of Winter. Aside from being an essential food source, White Cedar also provides good thermal cover in the Winter months similar to Eastern Hemlock (Tsuga canadensis). The White Cedar grow in tight groves helping keep the snow cover below shallower than surrounding open forests.

As White-tailed Deer move through White Cedar groves they tend to feed on all the green leaves from the lower branches within reach, often creating visible, generally uniform horizontal browse lines. These browse lines are a clear indicator of White-tailed Deer population in a given area.

 

 

4) Black Locust (Robinia pseudoacacia)

Black Locust is a tree that I have read described as a non-native invasive species which chokes out local tree populations. I have seen this native to the faraway distant (note the sarcasm) mountain tops of Pennsylvania to be an early colonizer of meadows and preventing erosion by stabilizing soil with an extensive root system. The bees love the beautiful and tasty flowers and it seems the White-tailed Deer appreciate the young shoots for Winter browse. The Black Locust was once planted for the valuable wood and also as a beautiful ornamental with their amazing dangling, pungent flowers. While the thorns may be irritating, they have developed on the tree to prevent too much herbivory by from the Deer while still giving something in the way of a good food. If only we could all learn good boundary making like this plant.

I noticed many of the individual Black Locust trees growing at Kinghurst were growing in open canopied clearings along the edge of the pine plantations, and this makes sense as they are intolerant of shade. I would imagine as more mature trees come down in that forest, more Black Locust will be coming up. They can do this quite easily, and they don’t need seeds. The Black Locust commonly spreads by sending up “ramets” or shoots from underground runners. If the Deer did consume a new shoot all the way to the soil, then the root would just send up another one.

 

 

5) White Pine (Pinus strobus)

For all it’s ubiquity, I don’t believe I have ever noticed White Pine being browsed by the Deer until this occurrence. I know this is a common occurrence detailed in the literature I have read, but I had not seen it before. I appreciate this assignment as I am now looking at this pretty common species in new light and noticing something that has likely been there forever, but is new to me. The White Pines I encounter also seem to be very large and in mature forests where the White-tails cannot reach the lowest branches but I am going to have to pay a lot more attention now just in case.

 

 

6) Common Blackberry (Rubus allegheniensis)

Similar to the Black Locust above, the Blackberry has a perennial root which sends up shoots. Instead of ramets, they are called canes which have a two year life span. Also similar to the Locust, Blackberry is intolerant of shade, I guess I am seeing a pattern. The Locust, and the Blackberry were both growing at the edge of the Pine plantation. This lets me know that the area is likely pretty sunny and that the Deer are moving through there.

White tailed Deer population thrive in edge spaces. The edges of a White Pine plantation, the edges of a field, the edges where suburban homes meet the green corridor protecting the creek. These are also prime places for the disturbance adapted plants such as Blackberry and the Locust and a host of other forbs. These help create a rich and varied diet for the Deer.

 

 

7) Red-osier Dogwood (Cornus sericea)

The Red-osier has a broad range, covering the boreal and temperate forest regions across the continent, so of course the White-tailed Deer, with a similarly broad range will encounter this shrub. Identified by the red bark on twigs and upper branches, a red which appears to grow redder when the Winter season starts to consider the shift to Spring. Often growing in wetter areas, good to look out for to know where the water might be in a snow covered landscape.
This shrub has taught me a lot over the years. So much so, that I purposely go check out the C. sericea when I am out tracking because it is very likely I will find sign of deer browse. I don’t know if it is the ubiquity of the plant or the blazing red which draw the deer in, but they appear to like this one a lot. I have seen some Red-osiers hit so hard they look as if a bonzai beginner just learned how to use their sheers and got snip happy, stunted and oddly growing, though without a clean cut. This is a good one to look out for on the land when wondering where the deer may be hanging out.

 

 

8) Black Cherry (Prunus serotina)

I associate many of the included species with medicinal action in the human body, and I wonder about these same actions with the Deer? I recognize we have different physiologies, but could they work similarly in an ungulate body as they do in a primate body? And if there is similar action medicinally, what about toxins? I have found White-tailed Deer browse on deadly poisonous Water Hemlock (Cicuta maculata) in the past yet did not find a dead Deer beside the plant. Same with Canada Yew (Taxus canadensis); feeding sign, but no dead animal. Do the Deer feed on the foliage of the Black Cherry or just the twigs? The leaves are full of cyanide and could be pretty harmful but perhaps the Deer have more suitable browse in the months when the Cherry leaves are present? I have also read that the twigs have cyanide present, but perhaps not as much as the leaves? Or maybe it just doesn’t bother the Deer at all and they’ll just eat what they want?

 

 

9) Sugar Maple (Acer saccharum)

Sugar Maple is a tree I could also get down with munching on. While a little bit bitter from the chlorophyll, the inner cambium still tastes pretty good. Yes, I have tried it. I have also eaten some buds on Sugar Maple in the past and I remember thinking they were palatable. Something I have also learned through the apprenticeship program is to identify Sugar Maples by looking at their the buds at the end of the branches, also called “terminal buds” (which happens to be the name of my nature gang). Sugar Maple terminal buds tend to narrow towards the tips and are more pointed and sharp feeling than, say, a Red Maple (Acer rubrum), which has rounder terminal buds. So the mnemonic “sugar sharp” can help us remember the Sugar Maples, and “red round” for the Red Maples.

 

10) Wild Grape (Vitis sp.)

A couple of weeks ago during an apprenticeship meet up at Dunby road, we had found feeding sign from White-tailed Deer on some feral Apples (Malus domestica) and some Grape (Vitis sp.) vines. These were very fresh and clear to see. Now fast forward to the outing at Kinghurst, where we struggled to find feeding sign on Grape for quite a while. I was excited when we found it.

I love eating the forked tendrils which grow at the ends of the Grape vines as they are crunchy similar to a Japanese Knotweed (Reynoutria japonica) have a slightly sour and bright flavour. I have eaten them on their own and in salads. I bet the Deer would also go for them in the Spring. But do they eat the leaves as well?

 

 

11) Hop Hornbeam (Ostrya viriginiana)

I had never seen feeding sign on Hop Hornbeam from an ungulate until this outing. I have seen individual pouches from the hop-like seed clusters opened by Eastern Chipmunks (Tamias striatus) but never had I seen the browsing on the twigs. Since then though, I have seen more ungulate feeding sign, namely Moose (Alces alces) up in Algonquin Park. I wonder if, like Porcupines (Erethizon dorsatum), Deer have specific browse that they tend to have individual preferences for? Do some Deer like the Hornbeam while most don’t find it palatable? Or is it just a case of my not seeing it before as most of the Hornbeams I notice are older, taller and have little to no lower branches within reach of the Deer to browse on?

 

 

12) American Beech (Fagus grandifolia)

American Beech seeds are tasty. I have found them hard to gather as a lot of seed cases turn out empty, and a bit tedious to collect so many tiny Beech “nuts” even when the cases are full. It takes a long time to gather even a few seeds. I remember once gathering about a cup of seeds with friends a few years back and between the three of us it took about an hour. I wonder if the Deer can smell it when the seed cases are full versus when they are empty? As for the twig browse, there was only a bit of browse at Kinghurst, but again, in Algonquin the Moose were hitting it pretty hard in some areas.

and one more bonus conundrum…

 

13) Digging?

I have seen sign of deer digging through the snow to access ferns and acorns before, but in this case there were no Oaks (Quercus sp.) or acorns around that I know of, and I couldn’t see much in the snowy debris of ferns which had been consumed. We were wondering if the deer were searching out roots of some kind, or perhaps they were feeding on some green shoots of grass, which however rare or unusual, has been observed in the past. Because I cannot determine exactly what the deer were after, I have included this as a bonus find, to be observed further in the future.

To learn more :
The Deer of North America by Leonard Lee Rue III. Lyons Press, 1997.
Trees of the Carolinian Forest by Gerry Waldron. Boston Mills Press, 2003.
Animal Skulls by Mark Elbroch. Stackpole Books, 2006.
Deer (The Wildlife Series, Book 3) edited by Duane Gerlach, Sally Atwater & Judith Schnell. Stackpole Books, 1995.

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More of the Scoop on Ruminant Poop (and Other Digestive Specialities)

This February 2025, while out with the Tracking Apprenticeship Group near Bell’s Lake, Grey County, we started using some terms for which I’m not totally clear of the meaning. I’d like to unpack them and share my learning here with you.

The words are rumen, cecal scat, ruminant and ungulate.

After a quick look up, I learn that an ungulate is simply an animal that has hooves. Horses, cows, deer and moose are all examples of ungulates.

While all ruminants are ungulates, not all ungulates are ruminants.

According to the Merriam-Webster Dictionary, ruminants are animals where food is ingested, held in the rumen, and then brought back up into the mouth to be chewed again. More specifically, they are herbivorous, even-toed, hoofed mammals (suborder Ruminantia and Tylopoda) that have complex 3- or 4-chambered stomachs. Examples of wild mammals in Ontario that are ruminants include deer, moose, elk, and caribou.

Moose are ruminants

When ruminants eat, they ingest their browse and after a very quick chew it is held in their rumen (the largest of their stomachs) where the cellulose fibers begin to be broken down by bacteria through fermentation. This material is then formed into balls (the cud) in the reticulum, which the animal chews a second time before swallowing, sending it down into the rest of the stomach for further digestion.

So the rumen is basically a fermentation tank for plant fibers. It makes sense then that we often find the contents of rumen in the prey remains from deer and moose; it is the largest chamber of the stomach and holds the biggest volume in proportion to the rest of their digestive tract (up to five gallons in a mature domestic cow). When a carnivore is consuming a ruminant, there is a lot of fluid and plant fibers in the rumen that they cannot digest and are left as waste.

Ruminants and most other animals including humans, have another stomach chamber that also helps break down tough plant fibers and this is called the caecum (cecum). It is the final chamber before waste is excreted. Like the rumen, the caecum allows for fermentation and nutrient and water absorption.

Learning how ruminants digest their food makes me wonder about porcupines, snowshoe hare and beaver.

According to a research paper from the University of Wisconsin, Stevens Point, beavers do have a caecum, close to the end of their digestive tract like ruminants, but they don’t have a rumen, and don’t chew the cud. Like rabbits and hare, however, they accomplish the task of breaking down cellulose and other plant fibers by being coprophagic. Coprophagy is when an animal passes stool after quickly consuming their food, and then re-ingests it in a safer restful situation where it can be chewed up more finely to allow for better digestion. It kind of serves the same function the rumen and reticulum. According to Dr. Uldis Roze, Professor Emeritus, in the Department of Biology, Queens College, porcupines, who have a relatively larger caecum, are generally not considered to be coprophagic.

Snowshoe hare are coprophagic

My final question relates to the caecal scat we often find from grouse. Do they have a caecum like ruminant mammals? Why do they have two different scats (the dry, fibrous kind and the goopy caecal kind (that looks kind of like caramel).

From what I was able to find online, most birds have two caeca, called cecal pouches. This division of the caecum is an adaptation to aid in their ability to fly.

While I did not find specific information on the cecal scats of grouse, I was able to find information relating to domestic hens, which are similar. The cecal sacs are emptied by both chickens and grouse when they become full of indigestible plant material in order to make room for other material as the birds eat. In the ruminants discussed earlier, the caecal contents are mixed in the regular faeces produced by the animal. In birds, they are excreted separately.

Ruffed grouse

Dry and caecal grouse scat

I am pleased to have learned more about these digestive processes and hope it is new learning to some of you as well. It is only scratching the surface, but when it comes to digging into poop, it seems to be prudent to be conservative in how much I bite off at a time!!

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Trailing Porcupine at Dunby rd

Porcupine trail heading towards the camera. Note the urine along the midline, and the trail leading right to the base of the Hemlock tree and then turning away.

The Earth Tracks tracking apprenticeship had been trailing a few different species when I ended up a little ahead of the group. I was following a clear Coyote (Canis latrans) trail when I came to another trail in the snow. This new trail appeared to come from a hill to my right, crossing over the Coyote trail and then meandered through a small low spring fed clearing where while mostly covered in snow, some spots were open shallow puddles with Watercress (Nasturtium officinale) growing. On the other side of this patchy wet area, there was another hill thick with wide trunked Eastern White Cedar (Thuja occidentalis) and Eastern Hemlock (Tsuga canadensis) where the trail led upwards. I knew who this new trail belonged to pretty much right away due to the oscillating midline that ran through the length of the furrowed trough in the snow. Other clues were the trail width, which averaged out to about 15 cm (5⅞ in), and the occasional spotting of urine that was sprinkled intermittently along the run. This was the trail of the North American Porcupine (Erethizon dorsatum), a common fixture in the forests of Dunby rd.

I had been thinking a lot about Porcupines over the previous few days. We had encountered some chews on a Tamarack (Larix laricina) with one of my adult programs at the Guelph Outdoor School, and had followed a trail through a lowland Cedar forest along the Eramosa River. Porcupine ecology had been front of mind and I had a few questions already before following this new trail, and of course they were renewed with each new finding. When folks from the apprenticeship decided that we should follow and focus on the trail more fully, I was all in.

I took some measurements of the strides of the Porcupine, and they came in with an average of 21 cm (8¼ in), which was pretty much average based on some of the books and what I have seen so far tracking Porcupines. Most of what I could make out on the trail appeared to be a direct register walk, with the hind feet landing in the spot where the fronts had just been moments before, though I did find a lot of the trail to be nondescript due to the fluffy loose snow. The trail seemed to both meander and appear like the Porcupine was going someplace specific. If I were to interpret the trail in my limited understanding, it would be that the Porky knew the forest, but was also looking for something along the way; A new tree? A conspecific friend, family member or mate? According to Donna Naughton’s tome Natural History of Canadian Mammals (2012), the Porcupines breeding season is between September to November, with a possible second heat, if the first was unsuccessful, stretching the season to December, possibly even January. With this broad period of time to be mating, it could’ve been that the indivdual we were following was looking for a mate, but they may well have also been just looking for something to eat.

According to Porky researcher Uldis Roze (1989), Porcupines tend to choose a preferred tree species and stick with it. Maybe it’s a Hemlock, or a Cedar. Maybe Sugar Maple (Acer saccharum), Trembling Aspen (Populus tremuloides), or American Beech (Fagus grandifolia). It appeared to Roze when observing the trails of a few different individuals that they appeared to have preferences, and these preferences were distinct among the individuals. For example, one Pricklepig (another common name) only tasted and fed on 17 Beech trees along their trail though the trail also encountered 37 Sugar Maples, 27 Hop Hornbeam (Ostrya virginiana), and 6 White Ash (Fraxinus americana). Another individual’s trail recorded a year later counted 7 Sugar Maples singularly fed on in a line that also included Red Maple (Acer rubrum), Striped Maple (Acer pensylvanicum), Mountain Maple (Acer spicatum), Hop Hornbeam, Beech and White Ash. These two individuals appeared to demonstrate individual taste and preference for specific species in their given habitat. Perhaps the Porc-épic (french common name) I was trailing was looking for their favorite flavour in the forest? The trunk in the photo above is of a Hemlock tree, but I wish I had noted every tree they had stopped to investigate.

I continued along following the trail and with most of the rest of the crew ahead I figured I could take it slow and inspect whatever I came across. Lucky for me, I came across a small narrow woody object in the middle of the Gaag (Ojibwe name, pronounced “ga’awg”) trail. When I bent to look, I realized it was scat!

The scat appeared different than I had seen in person before, but similar to some images I have found online and on some study calls. To my eyes it looked like three pellets stuck together with a mucousy coating. When I looked close at the content it looked like disorganized masses of pale brown wood chips. I didn’t take any notes but I remember the scat being about a 1 cm (⅜ in) in diameter. I don’t remember the length of the whole string, but from my photos I would guess at 7.5 – 8 cm (3 – 3⅛ in). I didn’t smell the scat, but I wonder now at if it would have helped me to identify the contents better?

I carried the scat with me as I walked along in hopes to show the rest of the group. I left the trail I was on, noting first where it went, and then sped up then to meet up with the group. Turns out everyone was just ahead of me staring up into a Hemlock tree where a Porcupine was resting in the upper branches. I didn’t really pay attention to this Porcupine much because the group mentioned that the trail I was just following led to another tree, a very large Maple a little ways down the hill. I had noticed this tree as the trail I was on previously was leading toward the Maple rather than the Hemlock where the group was standing. I handed off the scat and made my way towards the Maple.

The Maple was pretty large. Very tall with a fairly wide trunk. There were a couple of Tinder Polypores (Fomes fomentarius) growing above a large hole in the trunk, with a lot of human tracks around the base. In the snow just in front of the hole there was a pile of Porcupine scat which appeared stepped on by boots and compressed into the snow a little. I took some photos of the scat in the tree cavity and then turned on the front facing camera, reached my phone in and pointed it upwards. The first shot was dark and blurry, but once I turned on the flash I was not disappointed.

Looking at my phone I could see that there was a Porcupine hiding out, tucked up inside the bole of this huge Maple. I have seen this behaviour a few times, but I always find it pretty endearing. Especially when I looked close and saw part of the heel of the Porky’s right hind showing like the bottom of my slippers at home. It was a cozy nook for this gentle rodent to pass their time. I have since read that the Winter den sites are usually pretty close to their preferred feeding trees, so finding this other individual so close to the big Hemlock with the first Porcupine made sense. Perhaps they share this den? I have read that North American Porcupines are pretty solitary, but have also witnessed many denned up in the same den a few times. I quickly got up and away from the Maple immediately and made my way back to see the other Porcupine in the Hemlock tree.

Over the past 10 years of noticing and watching Gaagwag (Ojibwe again, but pluralized this time) I have seen many instances of them hanging out in and feeding on Eastern Hemlock trees. I can relate with my own appreciation for the Hemlock trees. I love their beauty, their ecology and their taste, both straight from the tree, or especially, in tea. I find the flavour to be piney with a whisp of fruit, sort of citrusy, and warming, and I am incredibly grateful to the Porcupine for their help in retrieving the needles for my teas. I’m just piggybacking on some of the baseline behaviours of the Porky. Since the bark of the Hemlock is high in tannins, the Porcupine feeds almost entirely on the needles and twig tips which contain fewer tannins. They nip the terminal branches and pull them in, eat the leaves and drop the branch. If any leaves remain on the dropped twigs which have fallen to the ground, they are often consumed by White-tailed Deer (Odocoileus virginiana) or by weird naturalists who like to make Hemlock tea.

I had a question about the quality of the forage. Do Hemlock branches really have that much nourishment? I recognize that Hemlock needles contain high vitamin C, but that isn’t enough to survive on, especially throughout the coldest hardest season of the year. What do the Porkies get from the Hemlock? In the book “Porcupines: The Animal Answer Guide” by Uldis Roze (2012), he writes that “Winter foods available to the North American porcupine contain less protein, more fiber, and more plant defense compounds (toxins to deter herbivory) compared with [S]pring and [S]ummer foods. As a result, [P]orcupines lose body weight and deplete stored fat layers”. Imagine that! You’ve gotta eat as much as you possibly can throughout the Spring, Summer and Fall so that when Winter comes, you don’t die because the trash you eat doesn’t provide enough actual nourishment to sustain you (I feel like this between Christmas and New Years sometimes). What a rough go. But the Porcupines have an advantage though; their caecum. What’s a caecum, also spelled cecum, you ask? A caecum is a section of the digestive tract at the junction of the small and large intestines where food that has been eaten ferments and bacteria and fungi breaks down the cellulose and lignin from plant materials a little more. This fermentation process helps pull out more nutrition and energy from the roughage that the Porcupines are consuming. Humans, lagomorphs, some birds, and even Lungfish have cecums, though they are not found in amphibians. For different species the cecum are shaped and function differently. For humans they are relatively small and connected with the appendix.
So the caecum helps break down the weakly nutritious fodder a little bit more to turn it into something a bit better. That helps a bit through the toughest time of the year.

Another neat thing to look for on the twigs dropped by Porcupines is the conspicuous angle of the cut which remains on the proximal end of the twigs. This distinct angled cut with characteristic “steps” which can be found on twigs nipped by both rodents (the family which Porcupines belong) and lagomorphs (rabbits, hares and pikas). Some folks call this a 45° cut, but it isn’t always though it sure comes close. Just knowing this angled cut and keeping an eye out can help us start to narrow in on who cut the twig.

This brings up a question for me.. what are the mechanics of Porkies eating? What are the teeth doing exactly? I have read that when Porcupines are feeding on cambium on a tree, they anchor in with the upper incisors while swinging their jaw and scraping with the lower incisors. This is the method for chewing the cambium, but not necessarily for the nipped twigs. What do the Porkies do to get the angled steps of the nipped twigs? This is going to require a little more research on my end as I can’t seem to find anything as of yet. Perhaps I’ll go out in the Spring and try a sit spot beside some Porcupines and see what I can sort out.

Lastly, it seems like some of my other questions don’t seem to be answered in the literature, like does the astringency of a bark, namely Hemlock with their high tannic content, change the scent of the Gaag’s urine? Maybe the researchers just aren’t as interested in urine as much as I am, but that’s a whole other blog post.

It has been a lot of fun to reflect on Porcupines over the past month, considering the part they play on the land and how they play that part. They are large, lovely and seemingly more abundant than they have been in the past – perhaps as more forests grow back in Southern Ontario, replacing the farmland which replaced the forests originally, then we’ll see more and more of the North American Porcupine.

To learn more:
Mammal Tracks and Sign by Mark Elbroch and Casey McFarland. Stackpole Books, 2019.
Natural History of Canadian Mammals by Donna Naughton. Canadian Museum of Nature and University of Toronto Press, 2012.
The North American Porcupine by Uldis Roze. Smithsonian Institution Press, 1989.
Porcupines: The Animal Answer Guide by Uldis Roze. Johns Hopkins University Press, 2012.

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“Do Those Prints Look “Foxy?” Tracking in Mono Cliffs Provincial Park

January 2025 Blog Post

On the weekend of January 11-12 2025, the Earthtracks Tracking Apprenticeship Group spent the weekend in the Orangeville area.  On Sunday we spent the day at Mono Cliffs Provincial Park, where we wound up and down the limestone valleys and ridges, being led by the animals who had gone before us, including primarily white tailed deer, fox and coyote.

We had a  close encounter with two deer who came upon where we were eating and were startled by our presence.  It was fascinating to try to piece together the order of events based on the prints, and try to determine the root cause of the deer’s movement in the middle of the day.

Were they driven towards us by coyotes?  Was one walking by when it picked up our scent and then became vigilant, bounding to get away from us?  Was the second deer alerted by the first?  Why did they run in opposite directions?  There were so many beds!  Somewhere between seven and nine, all within 50 m of our lunch fire.  We’ll never know exactly what happened, but reviewing the movement of the deer and coyote by examining their tracks was an excellent exercise in looking for the wisdom of the tracks.

We also had several opportunities to observe places where deer had urinated on the trail.  We enjoyed smelling the pine-scented urine, and postulated on which deposits had been made by bucks (in front of the hind legs), and does (between or just behind the hind legs).  

Does appear to squat a bit more than bucks.  Bucks seemed to “stretch out” their bodies a bit more than does while urinating. Think these pictures are both does.

While studying the deer sign was delightful (especially since it is my focal species), I was most interested in the coyote and red fox trails.  So often, as I track these two species at home, it often takes me a bit of time to settle on which species I am actually observing.

As I have been well-taught by Alexis, Byron and now Rob Baker, the tracker must be wary of using single factor reasoning when looking at prints to decide on what species is being observed.  When deciding between fox and coyote (two species commonly found in close association), there is sometimes overlap between print size, and fox and coyote use many, if not all of the same gaits.  

This blog is an attempt for me to  outline some of the distinguishing factors between these two species. 

Starting with foot morphology.  Fox and coyote are both canids and as such, both have four toes that usually register on both their front and hind feet. Both have feet that are symmetrical if bisected lengthwise. Both have front feet that are slightly larger than their hinds.  The sizes of their feet can overlap because a small coyote and a large fox may have feet that are the same size.  Both can appear to have an X in the negative space of their paws.  

Their feet do, however, have some features which differ.  The paws of the fox are much more furry than those of  the coyote. While it is hard to see this in snow, it is often quite visible in mud. Fox prints, both front and back, appear to be circular, while coyote’s front feet tend to be rounder, and their hind feet more circular.  Foxes have claws that are semi-protractable, so do not appear in prints as consistently as those of coyotes.

Note the fur on the pad of this fox

Another feature on prints of the front feet of the red fox, is a straight “bar” or “chevron” created by the backmost portion of the metacarpal pad.  The bar/chevron is absent in coyote prints. Mark Elbroch writes that ‘this is a key feature for quick identification’. 

The chevron or bar is clearly visible in this photo.

As someone who has only been tracking for three years, I rarely actually have been able to see the chevron. As with the hair, it seems easier to find in mud than in other substrates.  I sometimes see it in snow as well.  As in all of the tracking, part of the science is knowing what to look for.  

Ensuring I am not using single factor reasoning in identifying a species, my next step after looking at the prints of the animal, is to look at their gaits.  Both fox and coyote have a baseline gait of direct register trot.  Both will commonly side trot, and will move between other gaits depending on substrate and what they are up to (scouting, hunting, scent-marking and so on).  The difference between the species should be their stride and trail width; because coyote are taller and have longer legs than fox, it stands to reason their strides will be longer and their trails wider.

Looking at trail width and stride length, though I find once again that there is overlap between the species, regardless of the gait.  Measurements alone, it seems, cannot rule out one species or the other completely.

Another feature to consider is habitat.  Once again we find that both species are generalists who thrive in a wide variety of habitats.

What about social behavior?  Here is another factor to consider.  Foxes, outside of breeding season, are usually more solitary than coyotes.  Coyotes, although they may sometimes live alone, are more frequently found in packs.  At Mono Cliffs all of the coyote sign we observed appeared to be from multiple animals.  The fox, however, seemed to be alone.

A sure fire way to tell apart these canines is through their urine. Coyote urine, in my experience, really just smells like dog urine. Fox urine, on the other hand smells very much like a skunk.

So how to tell the difference between these two in the absence of urine?

Alexis likes to say that fox prints are more “dainty”.  He’ll also say, “that looks more foxy to me’.  

Until the day comes that I can look at a trail and say “that looks foxy”, I’ll have to rely on a combination of all the features above and more, to figure out who is at the end of that line of canine tracks ahead of me on the path.

Diana

All photos taken by me.

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Tracking in the Near North Winter Landscape

I was excited the weekend of December 14-15, 2024,  to host Earthtrack’s Tracking Apprenticeship group out of our home in Nobel, just North of Parry Sound.  My hope was to share the diversity and abundance of wildlife of this part of the “near north” with the group, most of whom were from Southern Ontario.

Two weeks before the scheduled weekend we did not have a flake of snow on the ground and I was a little concerned.   Three days later though, on December 4, bam!  Winter arrived and we had 2-3 feet of snow and were so thankful for it.

On Saturday we headed forty minutes north of town to crown land near the Naiscoot River.  Sunday, we stayed closer to town, exploring the forest and wetlands near Avro Arrow Road.

Over the two days we observed the tracks of seventeen different species including:

ruffed grouse, raven, northern flying squirrel, pine marten, fisher, moose, white-tailed deer, shrew, vole, wolf, red squirrel, red fox, white-tailed deer, river otter, short-tailed weasel, northern racoon and beaver.

We spent most of the weekend following fisher trails.  I was astonished by how active they are and how they weave back and forth and over and under and around trees and other landscape features.  At Naiscoot, we began following one fisher trail (presumably a female), but before long encountered a second trail that was much larger and in which we could really see claws in the drag marks.   While the trails did not obviously follow on top of each other, we did observe places where they crossed or were in close proximity.  

Early in the day we observed some ravens taking off from the forest.  This lead us to two different sites where a fisher had fed- one on a red squirrel, and the hind leg of a deer.

 

We wondered where the leg came from?  Road kill, predation?  Did the fisher bury it or did they dig up the cache of the original predator?  The meat had been cleaned from most of the bone, but there were not really any clear teeth marks on the bone.

It was so interesting to see how the gait of the fishers changed depending on snow depth and the purpose of travelling, for example a two by two lope in deeper snow, transverse lope in shallower snow, walk or trot when near to food sources.

 

 

One fisher print also reminded me of a time when I once confused a print of a fisher with what I had thought was a bobcat.  One missing digit can sure make a difference, and every pad does not always register!

 

 

 

 

 

 

 

 

 

I was also thankful to have the opportunity to observe and compare the off-set lope of a short-tailed weasel (on the left side of the picture), side by side with the bound of a red squirrel.

 

Finding a pair of wolf trails was also a treat.

 

At Avro Arrow, I had my first opportunity ever to track a pine marten.  There were some areas where the marten and fisher shared the same trail, giving us the opportunity to compare their prints side by side.  While they both moved in a two by two lope, the marten prints (pair two and four on this picture) were smaller with a more narrow trail width.

 

We also observed the sitz mark of a northern flying squirrel who had glided down from the trees and then landed leaving a tail drag across the snow before bounding away.

 

An additional treat was the trails of at least one (or more), river otters.  It was easy to imagine how they enjoyed travelling on their bellies as they slid across the landscape, whether it was over ice, snow, rocks or other natural features.  At one point, one even slid over the snowshoe trail we had left in the morning!

One of the best parts of this weekend for me was how emergent it was.  While we had a general idea of where we might end up but at both locations we let the tracks lead us.  We followed one species, and then the next as the tracks presented themselves.

I was struck many times, by how the land, when covered with new snow, is like a giant canvas.  The animals were the artists, leaving their unique tracks, signs and prints as they went about the business of surviving life in the winter forest.  How magical it was to spend time in this magnificent gallery with like-minded folks. 

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A Story Of Stones At Old Baldy

Bend over.
More.
Even more.
You may have to
sit
on the ground
with your head
almost
touching
the earth.
You have to look
a rock
right
in the eye.

from Everyone Needs a Rock by Byrd Baylor

I will do my best to keep this one concise, but covering 4 Ga (four billion years) in a short blog post is going to be a tough one, so please bear with me.

An Introduction

The Beaver Valley was shorn into the land through the cataclysmic pummeling of boulders and rocks propelled by massive riverine torrents spilling from the melting glaciers. Smashing their way across the newly exposed landscape which had been buried under approximately 2 km (~1.25 miles) tall walls of glacial ice, massive boulders, some carried by the ice from thousands of miles away, were being unloaded by the retreating glaciers and hurled across the landscape by epic rivers of incredibly cold meltwaters. These boulders bounced and slammed against the Georgian Bay Shale, and Manitoulin and Amabel Dolostone formations and a few other layers of bedrock before being washed out to the bottom of Georgian Bay, or settling along the valley floor. A broad river, much larger and much more fierce than the present day Beaver River, ran from valley wall to valley wall, eroding rock and depositing till picked up as the glacier repeatedly grew and lurched Southwards and ebbed and waned back Northwards over 2.5 million years of various states of glaciation. This till, carried from as far South as the Appalachian Mountain ranges to the Precambrian volcanic rock of the far North of Turtle Island, was strewn about the valley floor. The area looked like many modern mountain glacial moraines found today, full of rubble and stone, gravel and sands, with no visible life to be seen.

In time, and I mean a long time, wind blown spores of lichens and fungi along with seeds of cold hardy grasses and forbs began to colonize the rubble slowly changing the landscape from stoney valley to something akin to the present day tundra. Seeds of shrubs like willows (Salix spp.) and cottonwoods (Populus spp.) may have been first if we look to the tundra for example, growing quickly and dying back, building up a soil layer more suitable for later post-glacial successi0nal species. A couple of those species were White Pines (Pinus strobus) and Eastern Hemlock (Tsuga candensis) both lightweight wind blown tree species hailing from glacial refugium in Southern Appalachia. Maples (Acer spp.) migrated up from the mouth of the Mississippi, yet took a bit longer than the lighter and hardier conifers. As the world warmed and more faunal visitors returned to the valley, larger seeds were spread. Animals like American Crows (Corvus brachyrhynchos) and Blue Jays (Cyanocitta cristata) would be great acorn and chestnut dispersers, spreading the heavier seeds with their scatter hoarding caching behaviours. I have no records or research, but I bet the Huron-Wendat people who occupied the lands of the Beaver River, and those who likely were there before them, also had a big role in whatever diverse plant species began to spread through the valley. Slowly, very slowly the valley would be transformed into the deep lush forests whose soils and possible seedbank so eagerly desire to reclaim the land if let be.

How Can We Know What Has Happened On The Land By Looking At What Remains?

Dolostone

Marcus sitting with the dolostone.

An image of what Turtle Island/North America looked like 450 mya.

The photo above is of Marcus sitting against the sheer rock face at the top of Old Baldy. The stone is exposed dolostone which makes up Amabel Dolostone Formation. This dolostone is the product of the bodies of ancient animals which dwelt within the tropical Silurian sea about 450 million years ago.

Wait.. what?

Let me explain.

Dolostone is a sedimentary rock, formed from the calcium carbonate stored in the shells of some ancient brachiopods and cephalopods as well as from the carbonate-secreting algae which lived in a shallow tropical sea some 450 million years ago (mya). At this time our region of Turtle Island/North America was just below the equator and this gave lots of opportunity for ancient sea animals to flourish in the warm waters. The bodies of these animals were made up of the calcium carbonate mentioned above. These bodies which absorbed and used the calcium carbonate to create their hard shells eventually died and sunk to the bottom of the sea. Time rolls on and more and more bodies piled up. More carbonate was released into the aquatic environment Though time and pressure of oceans, through currents and more and more bodies piling up, limestone began to form. As the limestone begins to form a process of dolomitization occurs with the limestone becoming interspersed with magnesium found in the sea water. As the limestone becomes impregnated with the magnesium and the whole solution hardens, it all turns to dolostone.
This dolostone is very similar to limestone, yet with the addition of the magnesium, becomes very durable and is therefore less prone to erosion. While other layers of rock and shale may wash away after 400 million years, the dolostone remains as a remnant sign of the ancient sea beds. As near my home in Guelph, the dolostone cliffs of Old Baldy are like the fossilized dinosaur tracks through ancient creek beds in Texas – remnant traces of life from long long ago.

Glacial Erratics

Throughout the forests of Old Baldy there are many large boulders which do not conform to the dolostone bedrock which underlies everything. They just don’t match up with the rest of the rock that makes up the hill. If the hill is covered in rocks that don’t look like, or aren’t made up of the same stuff as the rest of the hill then we can understand, in tracking terminology, that these boulders are not part of the baseline of the landscape. We can then ask the questions, where are they from and how did they get there?

Some folks used to think that these massive rocks came from the great biblical floods of Noah. Wave action rocked the rocks back and forth for a while until the rocks ended up many thousands of kilometers from where they originated. In a distant sort of way they were right, but instead of water, it was ice.

The most recent glacial advance began about 95,000 years ago and during that period massive lobes of ice advanced Southwards across Turtle Island/North American swallowing and consuming almost everything in their path. As the glaciers covered the landscape, blocks of rock were torn off their home landscapes and carried by the glaciers only to be deposited someplace new. These rocks are called glacial erratics as they are wanderers (errare means ‘wander’ in Latin) across the land. They’re picked up, tossed around and left behind like I do with small sticks and stones on my own wanders. Now the cool thing about these erratics to a tracker might be that if geologists can figure out where the rocks have come from, then they can use these rocks to reconstruct and understand the path that the glaciers took.

I am still new to rock identification and when Alexis and I spoke about the boulder in the photo above, we both knew who to ask for more information: Bill the Bear, retired hydrogeologist and always curious and friendly tracker. I ended up writing him an email and asking what he could tell from looking at a photo of the rock. Turns out he could see a lot.

First he could tell by the colour and texture of the rock that it was likely volcanic in origin and because of that “very very far from ‘home’ ”. He wrote that it was likely composed of iron and magnesium that have been altered by chlorite on the rocks surface as result of being exposed to water over millions and millions of years. He suggested that if his assumptions were correct, then this erratic was likely of Precambrian origin. This would have been “part of the ‘mountain-building’ process, in what is now northern Ontario, which made the Himalayan mountains look like foothills!”
Bill mentioned Precambrian in origin which I think implies that this rock is from the Canadian Shield which is Precambrian igneous rock, which means it was formed between 3.1 Ga (3.1 billion) to the beginning of the Cambrian Period, about 538.8 million years ago. This is a massive span of time, inconceivable to me really, but somehow still awe inspiring. The word igneous means that this rock was “born of fire” or as Bill mentioned, volcanic in origin.
Rocks of volcanic origin are produced in a variety different ways. In the book Ontario Rocks by Nick Eyles, the author states that igneous rocks are formed when magma cools and becomes solid. The grain size of the the rock depends on how fast the rocks cool, with finer grains showing up in rocks that have cooled quickly and course grain in magma that has cooled slowly. This rock was rough to the touch and in my follow up research gets me thinking of a type of rock known as gabbro which is a slow cooling rock formed from molten magma from deep within the Earth’s crust. I have read that these rocks would have become solid more 1 Ga (1,000,000,000, one billion) years ago, and was eventually brought to the Earths’ surface by uplift caused by tectonic shifts and erosion caused by weather, water and wear on the land. Then again the glaciers picked it up and plopped it down at Old Baldy perhaps around 12,000 years ago.

I havn’t been able to figure out more about this rock in particular but I am in search of anything more that might flesh out the details a little more. This might take some time, but I guess that’s what this is all about. The rocks will wait.

Post Glacial Isostatic Adjustment

As mentioned above, the ice sheets around the area of Old Baldy was covered in these massive mounds ice approximately 2km thick. 2000m. 4 CN Towers. 11 Seattle Space Needles. They were @#&$*+!! huge! It’s hard to imagine how tall they must have been, let alone how much they weighed. But they weighed a lot. According to one source, a cubic meter of ice weighs about 916 kilograms (2020 pounds), so it’s kind of interesting to think of what 2000 m of ice might weigh, but really that’s just one spot. Imagine these ice sheets covering all of the Northern parts of Turtle Island/North America and almost the entirety of Canada. To quote Wallace Shawn’s character Vizzini in the 1987 hit The Princess Bride, “Inconceivable!” I can’t find actual numbers but lots of adjectives are thrown around, such as “enormous,” or “massive,” and “incalculable” are a couple of good ones. The glaciers weighed so much that they depressed the Earth’s crust and mantle below. In Northern Ontario near Hudson’s Bay there are estimates that the land was pushed down about 270-280 m (~300 yards), though less in Southern Ontario. This made the land adjacent to these depressions rise as well, like a crest or plate when considering pressure releases in animal tracking.

But something amazing happened as the glaciers started to retreat. The land which had been previously depressed by the incredible weight began to rebound and rise up, and much the adjacent lands which had lifted began to subside (sink down again). This process of rebounding land is called Post-Glacial Isostatic Adjustment. Though it has had many other names over the years such as glacial rebounding, isostatic rebound or crustal rebound, post-glacial isostatic adjustment makes the most sense in that the land isn’t just lifting up again. Some land is subsiding (sinking), some land is being pushed away from where it once was, and this is causing changing sea levels, and even shifting the Earth’s rotation. Post-glacial isostatic adjustment translates to “Changes in equilibrium of the Earth’s crust after the glaciers” which is a more honest and accurate interpretation of what the names are trying to describe. To get back to the point, through these changes of the elevation of the land in the Old Baldy/Blue Mountains area, the land in that area has risen over 15 m since glaciation and is still continuing to rise at a rate of about 15 cm per hundred years or 1.5 cm per decade. It’s not that much in the grand scheme of things, but I still think it’s pretty wild.


When researching geology in the context of tracking the landscape I am reminded of a phrase that Alexis Burnett often attributes to one of his teachers Tom Brown Jr., and I hope I am not misquoting here.. “The Earth longs to be flat, everything else is a track.” A mountain is the track of tectonic plates shifting and smashing into one another, an odd stone in a field the sign of a glacier, and an Oak (Quercus sp.) tree is the remnant sign of a seed possibly dropped by a Blue Jay many years before.
I’ve been thinking about how in a world of calamity and upheaval, extinction and war, that sometimes there is a grounding in remembering the ancient body that we all come from.

Researching and working towards a deeper understanding of the geology of this venerated hill has actually been a peaceful reflection when places of peace have been so hard to find. I recognize that these are epic cataclysmic histories, but the stories held in the stones at Old Baldy have brought about a deep sense of peace for me when it seems so lacking in the world right now. Maybe it’s the disconnect of me not being present for the upheaval and torrent of glacial meltwaters and crushing sheets of ice, but doing the research, piecing together clues, and imagining the magnitude does create a profound sense of wonder and awe, a stupefying amazement in the unveiling of a billion years of mystery written on the body of the hill. I deeply appreciate the work and practice of listening to the stones and tracking the beauty of the land.

To learn more :
Walking Through Time : Exploring Niagara Escarpment Geology in the Beaver Valley Bruce Trail Section by Beth Gilhespy, M.Sc. Self published, 2023.
After The Ice Age : The Return of Life to Glaciated North America by E. C. Pielou. The University of Chicago Press, 1991.
Ontario Rocks by Nick Eyles. Fitzhenry & Whiteside, 2002.
Geology and Landuse Between Guelph and Hamilton: A Self-guided Tour by Chesworth, W., Martini, P., McCarthy, P. and Sadura, S. Dept. Land Resource Science, University of Guelph, 1996.
Ancient Earth interactive globe – see what the Earth looked like from 750,000,000 years ago up to now
NASA’s video on Earth Rebound and Subsidence
Ontario: The Geology of Isostatic Rebound – Rising Land

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Mudflats are For the Birds!

On our most recent Apprenticeship Weekend, October 26-27, 2024, we spent seven hours tracking along an expanse of mud where the level of the Grand River had been lowered to accommodate spring runoff.  During that time we probably covered only a few kilometres, but each of us crossed paths with hundreds, if not thousands, of prints, most of which came from birds.

 

I’d like to go through some of the bird species we encountered, their distinguishing features and in some cases, associated behaviours.  I’ll go from the largest to the smallest.  My main source of information was the book Bird Tracks by Jonathan Poppele, published by Adventure Quick Guides.  Additional information came from Bird Tracks and Sign by Mark Elbroch and Eleanor Marks, Stackpole Books.

 

 

 

 

The largest print we observed was of a great blue heron, which its longest point, was 8” long.  The length of the print confirmed it was a blueheron as other large birds who would also be likely in the area (for example sandhill crane), have prints that are much shorter since they lack the long toe one (the hallux in birds).  The only species who might overlap in configuration and length is the bald eagle.  While we did see an eagle, we did not locate their prints, which are much more bulbous with talons registering further from the print due to their length and curvature.

 

 

 

 

 

 

 

 

 

 

Canada goose prints were abundant on the mudflats.  The tracks that interested me most were prints where there was a lot of weight on the toes, long strides and then an abrupt end to the line of tracks. The goose was running and then took off!  The prints looked so unusual as they showed striations or lines from the leading edge of the webbing.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Interestingly, only a few hundred metres from the goose take off, Tamara spotted another take- off point, this time from a crow.  Crows, ravens and bluejays, like all corvids “share a distinctive track feature: toe three angles to the inside and hugs toe two”( Poppele).  The crow, being much lighter and more agile than the goose, was able to take off from a standstill with a big push down as evidenced by the two prints beside each other, pushed deeply into the mud.

 

 

 

 

 

 

 

 

 

Another track that we observed many times was of the greater yellowlegs.  This is not a common shorebird normally, but was likely in the area on their migration.  A few of us were fortunate to have been close to one individual as they walked along the shore probing the mud.  Through my binoculars the legs were indeed a very bright yellow.  The yellowlegs prints could be distinguished from other shore birds because of their size,  slender toes and lack of palm showing in the print. 

 

 

 

 

 

 

Photo credit: Byron

 

Next in order from biggest to smallest were prints of  killdeer.  These prints were more abundant than the yellowlegs and could be distinguished because they were almost equal in length and width, were asymmetrical, tended to be pigeon-toed in their movement and lacked a hallux.  We observed several killdeer both flying and walking.  Like the yellowlegs, they were likely not resident, but rather were on their migration journey.  Photo credits: Byron

 

 

The final shorebird print we observed was of a sandpiper (likely spotted).  This print was smaller still and less abundant than the other shorebirds.  Note- this image was taken from a different location

 

 

 

 

 

As we observed these prints and many more (including red fox, opossum, beaver, mink, racoon, skunk, white-tailed deer, muskrat), I was thankful for mud, clay, clear skies, knowledgeable mentors and friends who enjoy connecting to animals through their tracks as much as I do.  Looking forward to our next adventure together!!

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Tracking at Saugeen Shores, 2024.09.28

The most recent outing with the Earth Tracks tracking apprenticeship group was too much. I can’t even figure out what to start writing about. Maybe it should be about the Northern Harriers (Circus hudsonius) we saw swooping low over the grasses and sedges out along the peninsula? Or maybe the Sandhill Cranes (Antigone canadensis) and Great Blue Heron (Ardea herodias) wading out across the small inlet. I think I’ll start with the confusing ones…

When the apprenticeship visited the Saugeen Shores, I got confused. How do we tell the difference between Sandhill Crane tracks and Wild Turkey (Meleagris gallopavo) tracks? I am sure it is simple to some folks, but I still get mixed up every time I encounter either of their tracks where species could overlap in the same habitat.

Let’s start with my quick measurements. I sadly only wrote down one length measurement and that was 8 cm. The widths I wrote down were 9.5, 11.5 and 12 cm. While the length measurement does not fit for either Wild Turkey and the Sandhill Crane according to Elbroch and Marks, the widths do. Some of the tracks I thought I could make out a hallux, or toe 1, but I wasn’t sure as there were many of the same track in the area, often overlapping one another.

All in all, Sandhill Crane didn’t seem as likely creators in light of all the other factors mentioned above. Instead I believe the tracks were made by a mixed group of older and younger (considering length of some of the tracks) Wild Turkeys.

These weren’t the only bird tracks we saw…

Edited photo of Greater Yellowlegs we saw taken through my monocular (photo edited for better display online).

I first noticed the Greater Yellowlegs (Tringa melanoleuca) calls before seeing them. They reminded me of a Killdeer (Charadrius vociferus) call in timbre and frenetic energy, but different in cadence and length. We were on the beach where I had just been looking at Killdeer tracks moments before and wondered if it was them, but when they were pointed out later it made more sense that these were the Greater Yellowlegs based on their size. When I got out the monocular my eye was attracted to their long bill and airfoil-ish, football-like, body shape.

Andy and I watched two of the Yellowlegs run and stutter about in the shallow water of a narrow shallow channel running between estuaries at the edge of Lake Huron. We waited until they had made their way around a small sand bar and when they did we went over to where they had just been in search of tracks.

Greater Yellowlegs tracks are similar to Spotted Sandpiper tracks, which come in at small 2.2 – 2.5 cm (⅞ – 1 in) L by 2.5 – 3.2 cm (1 – 1¼ in) W, which is a noticeably smaller. Jonathan Poppele says the same as Elbroch and Marks, that the metatarsal will rarely show on the Yellowlegs, but does tend to show up on the Spotted Sandpiper. Good to keep these in mind in case I see either of these two in the future.

The Yellowlegs tracks kept us busy for a while, but we kept going as we had so much more to explore. I walked back to grab my bag and revisit something else I had taken a look at earlier. Some skeletal remains of some sort of fish. A couple of the bones we found looked like they could be a spinal column. A couple looked like saw blades and we even cut some sedges with them, just to see how well they would cut. Some I couldn’t figure out at all. And then there were a couple which struck me both as familiar and as very strange. Two identical bones, the same bone yet likely situated opposite each other in the body, curved with small tooth-like tubercles or nodules on them. Here are some photos, one from the day of, and some taken later in my backyard.

Gill filaments and gill rakers on a Rainbow Trout (Oncorhynchus mykiss).

Most fish have gills. Some have lungs, but we’re going to discuss the gills so I am going to stay on point. How do gills work? Well the fish draw in oxygenated water in through their mouth. They then pump this water over the gill filaments so oxygen can enter the bloodstream. These same gill filaments also allow oxygen poor water to leave through the same gill slit.
Most bony fish have five boney gill arches, sometimes called branchial arches, on each side of their heads. The gill arches support the gill rakers on the anterior side (closer to the front of the fish) and gill filaments on the posterior part (closer to the tail). Gill filaments again are where gas exchange occurs. The gill rakers are little protrusions which “rake up” small particulate which can be consumed by the fish and may also be for prey retention in the case of a fish consuming smaller stuff. Think of them both as filters, one for gas, the other for food.

1,1,3-3,1,1 dental formula of the European Carp, counting from the outside in on the near gill arch, and then the inside out on the far gill arch.

For some fish, the fifth gill arch is modified. There are no gill filaments. Instead there are boney tubercles are called pharyngeal teeth. These pharangyal teeth are probably modified gill rakers which have evolved to serve a new function. They sit in the back of the throat of a few different fish species. They aren’t teeth anatomically, but they serve a lot of the same function as teeth do. They help fish to crush and break down small mollusks and crustaceans or even tough vegetation that they are consuming as well as help to filter whatever is going down their throats. Based on the size of the teeth and the other bones we found, I think we identified this individual as a carp.

Carps are in the family Cyprinidae which also include chub, dace, shiners, true minnows, koi, and Goldfish (Carassius auratus). They all lack oral teeth but they do have pharyngeal teeth (as do some other families as well), and these pharyngeal teeth display with such diversity that they can be used to identify different species. There are even pharyngeal teeth formula to help with this identification, but for now I only know the this individual species dental formula : 1, 1, 3 : 3, 1, 1, counting from the outside in on the near gill arch, and then the inside out on the far gill arch. Based on the teeth we found, I am going to call this fish a European Carp (Cyprinus carpio), also known as the Common Carp. They are a non-native species which loves the warmer vegetated shallows of the Great Lakes and many of the rivers which spill into them, such as the Eramosa River where I live. European Carp teeth have been described as having the same 1, 1, 3:3, 1,1 dental formula, and the teeth themselves are “robust, molar-like with crown flattened or somewhat furrowed”. Still no idea how they died and wash up on the beach, but they were there, picked clean, likely by some of the birds in the area as few bones which were present were broken, which is pretty common sign for mammals scavenging.

The thin drag marks left by the outer edges of the tail projections (called uropods) are usually an obvious distinguishing feature of crayfish (Astacoidea) trails. Trails appear as two well-spaced parallel lines, with tracks from the legs registering outside these lines. Crayfish walk primarily on the four pairs of legs (periopods 2 through 5) behind their claws (periopod 1), the first two of which have two fingers at the end that form small pincers. Tracks often register in groups of three or four, depending on whether the last pair of legs leaves distinguishable imprints… On good substrates, the pincers on each of the front two leg pairs register as two distinct dots.

Looks right, sounds right, but I wish I could know the direction of travel. From looking at the drag marks in the dots, again created by the legs, I believe that the crayfish was heading from the top of the image towards the bottom of the image. Why do I think this? Remember snow? Well, when say a White-tailed Deer (Odocoileus virginianus) or a Coyote (Canis latrans) is moving through the snow I often see a slope descending from where the animal is moving forward and about to put their foot down, and then a sharp lift out of the deep snow with incredibly little to no ascending slope at all. While this sand was not deep snow, I believe the same results happen in various substrates, even with different types of bodies creating the marks.

Another cool invertebrate trail we found looked muddy and as if little bits of sand had been pushed up from below to form a crumbling esker, like a tiny mole tunnel. We were looking at it wondering who could have made it when I remembered Shane Hawkins saying she once found a spot where a Common Snapping Turtle (Chelydra serpentina) trail suddenly ended in a strange muddle oval-circle shape. She wondered if the turtle had dug themselves in so she started to dig, and to her amazement, she found the resting turtle deep in the mud. I knew this wasn’t a turtle trail but decided it would be worthwhile to try and dig throughout a neighbouring tunnel and see if I could find something living inside it. And I did!
I dug out a small, maybe 22 mm long, wet, soft, squishy larvae which immediately reminded me of a firefly larva with it’s strange somewhat segmented abdominal terga plates, extending and retracting head. Firefly are in the Coleoptera order (beetles) and this little dude looked a lot like a beetle larva so that was my first guess. It isn’t a very useful guess though. Coleoptera make up about 40% of all known insect species, and about 25% of animal life on Earth. To put it another way, 1 of every 4 species of animal on Earth is a beetle. So it could be a beetle or it could be an larva that looks somewhat similar.

It is likely that the species we found is in the genus Stratiomys. I ended up posting the photo above on inaturalist with the suggestion of Stratiomys as the genera and another user confirmed the i.d. I then looked up the user and it turns out he works as a taxonomist with a special interest in Stratiomyidae! Inaturalist is a very useful resource. I would suggest looking using the website/app, especially for difficult i.d.’s like insect larva.

We kept on with our day, meaning we walked another 10 meters or so and then stopped again to admire another trail.

The trail could be described as alternating patterns of two rows of dots laid atop one another. We interpreted this as a front foot landing and then a hind foot. But which was which? And which way was the animal going? And who was this animal?

When I see a trail like this, a trail that does not widen or narrow along the entirety of the length we can see, as I did with the crayfish, I immediately think of a body that has a fixed width, or at least has parts of the body that cannot get any narrower or wider regardless of how fast or slow they are going. Alastair measured the trail width at about 20 cm (~8 in). This is wider than any invertebrate that I know of and must denote another, larger species. I think we all understood almost right away that this was a trail left by a turtle. Their spines cannot flex and they cannot narrow or widen their trail widths. But which turtle was it? There are records of Common Snapping Turtles, Midland Painted Turtles (Chrysemys picta ssp. marginata), Spotted Turtles (Clemmys guttata), Wood Turtles (Glyptemys insculpta), and there may be Blanding’s Turtles (Emydoidea blandingii) and maybe Northern Map Turtles (Graptemys geographica) in the area. All of these turtles but one are too small to make such wide of a trail. The Midland Painted Turtles trail widths according to Filip Tkaczyk in his book Tracks and Sign of Reptiles and Amphibians are 10.16 – 16.76 cm (4 – 6.6 in), which is too small for the trail we found. The Common Snapping Turtle trail width is 20.32 – 26.67 cm (8 – 10.5 in) which fits well for our trail we found. I do not have the numbers for the trail widths on any of the other species listed above, but I am fairly certain that the Snapper is the largest turtle in the area, so the trail is likely from a Snapping Turtle. I don’t remember if there was a tail drag or not, but the presence of a tail drag can help with the identification, as well as the plastron drag. The plastron is the bottom part of the turtles shell on the underside of the turtle. Some turtles drag their plastrons, while others tend to lift theirs off of the ground when they walk. Painted Turtles have a relatively wide plastron that often drags when they walk, where as the Snapping Turtle raises their body as they walk and the plastron does not show until moving through deeper substrates or when coming to a stop. Again as we saw no evidence of a plastron drag this too points to a Snapping Turtle.

Now, more questions. What was the direction of travel, towards or away from the water, and how do we know?

Snapping Turtles have 5 toes on the front feet and all of them tend to show up in ideal substrates. They also have some big long and thick claws which really dig into the sand or mud or other substrates you find them in. Front tracks also tend to be turned toward the center of the animal/trail at about a 45° angle, which makes it easier, sometimes, to figure out fronts from hinds. The hind tracks also have 5 toes, but usually only 4 of the toes register. The hind tracks do not turn inward in that same 45° angle as the fronts do, but instead face forward towards the direction of travel.

Alastair took the time to describe the trail in detail for all of us noting exactly this, that the front foot claws were angled towards the center of the trail, and that the rear foot would be pointing in the direction of travel, which meant the Snapping Turtle was walking up and out of the water towards the higher vegetated ground.

We sat down for lunch around the spot of the Snapping Turtle and watched a Ring-billed Gull (Larus delawarensis) make some tracks as we ate and then moved on.

I have to admit that we saw a lot more stuff, fascinating discoveries, each one deserving their own lengthy blogpost but I look at my calender and see that with another tracking weekend coming up in only a few short days, I feel like this one needs to be brought to a close. Perhaps someday I’ll get back to some of the other things we saw but for now this is the end.

Now I just can’t wait to get back to Saugeen to see what new we’ll find next time.

p.s. Did you know that you can estimate the age of a fish from counting the growth rings on their scales? Similar to trees in cooler climates, fish grow slower in the winter and the growth rings show up closer together and create the appearance of a thicker or darker ring. These thick or dark “winter rings” can be counted to determine a fish’s age! Now I have to start looking at scales as well as teeth.

To learn more :
Bird Tracks and Sign by Mark Elbroch and Eleanor Marks. Stackpole Books, 2001.
Bird Tracks by Jonathan Poppele. Adventure Publications, 2023.
Freshwater Fishes of Ontario by Erling Holm, Mary E. Burridge, and Dr. Nicolas E. Mandrak. ROM, 2010.
Pharyngeal Teeth video by Timothy Spier
FishBase entry on Cyprinus carpio
Tracks and Sign of Insects and Other Invertebrates by Charley Eiseman and Noah Charney. Stackpole Books, 2010.
Tracks and Sign of Reptiles and Amphibians by Filip Tkaczyk. Stackpole Books, 2015.
A Guide to Common Freshwater Invertebrates of North America by J. Reese Voshell, Jr. The McDonald & Woodward Publishing Company, 2002.

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Wolf Spiders at Sauble Beach, September, 2024

On the weekend of September 28-29,  this year’s tracking apprenticeship group spent two days in the Sauble Beach area.  On the 28th, the majority of our time was spent along the lake shore where we were able to observe a variety of prints in sand, mud and silt that was either wet or in the process of becoming dry.

On the 29th, we moved inland away from the lake where there was much less moisture.  The dew from the night before, while no longer visible as drops, had dampened the sand enough that in the morning when we arrived many prints were very clear, telling the story of coyote, fox, squirrels, mice and other residents who had been active during the preceding evening or early morning. 

 

 

These squirrel prints were very clear in the dew-dampened sand

 

 

 

 

 

 

 

 

 

 

The sand allowed us to clearly see the recent movement of a fox as they went back and forth across the area.  We were able to compare fox and coyote tracks and analyze gaits and some movements.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

The sand also beautifully held onto tracks and trails of smaller creatures including insects, spiders and snakes.  It was these that caught my attention as they were so different from the prints of mammals, and are rarely seen in my neck of the woods where I don’t often see fine-grained sand.

The first new sign that caught my attention was these. 

 

 

Once the first was noticed, we spotted several more.  According to Tracks and Sign of Insects and Invertebrates by Eiseman and Charney, this hole and it’s accompanying tube are likely the den of a “wolf” spider.

As a little girl, “wolf spiders”,  like “fire ants” to the children I spend time with today, were sort of mythical.  Any spider that was big and hairy we called a “wolf spider”, but I have never had the opportunity to learn more about them until now.

Wolf spiders belong to the genus lycosidae (almost 2500 species known worldwide),  and are known for having keen eyesight (and eyeshine when put under a light at night) and are both hunters and opportunists.  They do not use webs to trap their food, and will hunt both in the day and at night.  Females of this genus carry their egg sacs in their spinnerets, occasionally putting them down when hunting.  Once the eggs hatch, the mothers carry them on their back or bellies until they disperse.

Three distinguishing factors that help identify wolf spiders from other spiders are the placement of their eight eyes, presence of tarsal claws, and the angle at which they carry their fangs (chelicrae) (pointing towards each other).

 

 

While wolf spiders can be found in leaf litter, under rocks and even in sphagnum moss, some species, like the ones in the sand in Sauble, build a burrow.  According to Eisemen and Charney, “Many wolf spiders make silk-lined burrows in the ground with circular entrances.  When excavating, they tie the soil together in little pellets which they carry in their chelicrae and drop a short distance from the burrow entrance.”  Some species also create a “turret”, as we saw at Sauble.  These spiders will also block the entrance to their burrows for the winter.  Wolf spiders have also been known to carry their egg sacs up to the mouth of their burrows to sun them.

An additional sign that may be found around wolf spider burrows are their footprints as they make hunting forays as I believe can be found in the image above.

I look forward to learning more about wolf spiders and other invertebrates who leave their trails and sign in the sand in the future.

 

 

 

  

 

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