Snake Road

Mesic bluff base forest along “Snake Road.”

Last fall, my good friend Richard Thoma and I visited “Snake Road” is a famous snake viewing area in southern Illinois—part of the LaRue-Pine Hills/Otter Pond Research Natural Area. Early October is prime season for viewing snakes there, principally northern cottonmouths (a.k.a. water moccasins—Agkistrodon piscivorus) as they move from the wetlands on the west side of the road to the towering limestone bluffs on the east side seeking crevices in which to shelter for the winter. With a string of cool nights and sunny skies and a forecasted high of 78°F, we couldn’t have picked a better day to look for them.

Shafts of morning sunlight stream through the forest.

We arrived a little after 9am, so conditions were still a bit too cool for the snakes. Shafts of morning sunlight streaming through the trees were a sight to behold, and we used the opportunity to notice some plants that we’d not seen before, including two species of goldenrod—i.e., Solidago caesia (bluestem goldenrod) and S. flexicaulis (broadleaved or zigzag goldenrod), Decodon verticillatus (swamp loosestrife), and Laportea canadensis (wood nettle). I noticed small green berry-like structures on some of the latter, which I at first took to be fruits, but something about them said “gall” and I cut one open to find a small insect larva inside verifying this to be the case. I presume this to gall to have been caused by Dasineura investita (wood nettle gall midge) in the family Cecidomyidae.

Solidago caesia (blue-stemmed goldenrod) in mesic bluff base forest.
Inflorescence of Solidago caesia (blue-stemmed goldenrod) in mesic bluff base forest.
Solidago flexicaulis (broadleaved or zigzag goldenrod) in mesic bluff base forest.
Inflorescence of Solidago flexicaulis (broadleaved or zigzag goldenrod) in mesic bluff base forest.
Decodon verticillatus (waterwillow or swamp loosestrife) in Mississippi River floodplain oxbow lake.
Laportea canadensis (Canada nettle or wood-nettle) in mesic bluff base forest.
Gall on Laportea canadensis (Canada nettle or wood-nettle), presumably caused by Dasineura investita (wood nettle gall midge).
Dissected Dasineura investita (wood nettle gall midge) gall on Laportea canadensis (Canada nettle or wood-nettle) revealing the larval inhabitant.

As we hiked south along the road (closed to automobiles during spring and fall to protect the migrating snakes), and especially when temperatures climbed above 70°F, we began looking in earnest for snakes, reasoning that they might best be found by searching along the base of the bluffs and in nearby crevices. We searched one particularly promising rock ledge without success, then encountered a spring draining from the main bluffs and followed it to the base, where we split up and looked along the base in both directions. My direction took me around a bend and up the hillside, with many nice-looking crevices but no snakes in them, and when I reached to top of the exposed bluff face I turned back and retraced my steps. Just after reaching the bottom I noticed movement near where I’d taken a step, and there it was—a gorgeously-marked juvenile cottonmouth! I called Rich over, and together we spent about a half-hour taking turns trying to get the perfect photograph of the snake while trying to minimize the degree to which we disturbed it (lest it make a dash for the nearest crevice, or worse yet, take a lunge at one of us). The majority of the photos shown here are of this individual, and the only photo I wish I would have gotten was one with a fully-extended, flickering tongue.

Juvenile northern cottonmouth (Agkistrodon piscivorus).
Juvenile northern cottonmouth (Agkistrodon piscivorus).

Our spirits buoyed by the experience, we bushwhacked back to the road and almost immediately encountered not one but two fully mature individuals—both having already lost the distinctive patterning seen on the juvenile but beautiful nonetheless. We spent more time photographing these as well, as we were able to get several great shots of the distinctly marked throat and mandible as they reared their heads in cautious defiance. I used the big camera exclusively for these shots, as they were much too large and I would have had to have gotten much too dangerously close to photograph them with my iPhone (look for photos to appear eventually on my natural history blog—‘Beetles in the Bush’).

Further south we found an exposed bluff face very close to the road, and several additional mature individuals were seen there—two deeply ensconced within their chosen crevice but one fully exposed (two photos here) who even cooperated by gaping his mouth in alarm to show off the cottony-pink tissues inside.

Adult northern cottonmouth (Agkistrodon piscivorus).
Adult northern cottonmouth (Agkistrodon piscivorus) with mouth agape, revealing the cottony-pink tissues inside that give rise to its common name.

In all, we would see nine individuals by the time we hiked to the southern parking lot and turned around, and on the way back, not trying nearly as hard and making a more direct line to the car, we would see another five individuals (two of which could have been individuals we’d seen on the way out) for a total of 14. We also watched in amazement as a tiny juvenile eastern yellow-bellied racer (Coluber constrictor flaviventris) chased down a fly on the road before dashing back towards the forest, and we were particularly amused by a nine-banded armadillo (Dasypus novemcinctus) who lumbered stupidly out of the underbrush straight towards us, completely unaware of our presence until Rich made a sudden movement with his hand that sent the little brute scurrying back into the underbrush.

Nine-banded armadillo (Dasypus novemcinctus).

Almost as we reached the car, we found a ribbon snake (Thamnophis sauritus) stretched out across the road. Snake sightings notwithstanding, the return hike back to the car was not nearly as enjoyable as the hike out, as by this time quite a number of other people had shown up and we no longer had the place to ourselves. I can only imagine what it must be like here during the weekend! Nevertheless, we couldn’t have imagined a more successful and enjoyable outing than the one we experienced today.

©️ Ted C. MacRae 2022

Botanizing at Prairie Fork Conservation Area

Restored claypan prairie around Crow Pond.

Today’s outing for the Webster Groves Nature Study Society (WGNSS) Botany Group was Prairie Fork Conservation Area, a newish Missouri Department of Conservation (MDC) property that is open to the public only by appointment. The 911-acre property lies within the historic 9-mile long prairie of Callaway County, Missouri—namesake for Nine Mile Prairie Township. Prior to MDC ownership, the property was owned by Ted Jones, son of the founder of Edward Jones Financial Company, and his wife Pat, who began dedicated conservation practices beginning in the 1950s. Obviously, conservation in those days—with its reliance on plantings of many now-invasive exotics such as Lespedeza sericea (sericea lespedeza), Lonicera mackii (bush honeysuckle), and Elaeagnus angustifolia (Russion olive), meant something very different than it does today. Nevertheless, the foresight and generosity of Ted and Pat Jones ultimately led to the creation a conservation area where more than half of its area has been or is being restored to claypan prairie resembling as much as possible its presettlement character.

Crow Pond.

The group engaged in two short hikes—the first through several garden plantings and then at the interface between tallgrass prairie and upland forest surrounding the perimeter of Crow Pond. Almost immediately we were treated to the sight of Gentiana andrewsii (closed gentian) in bloom. To the uninitiated, the mature flowers appear to be still-unopened buds. In fact, the corolla in this species remains closed, and the flowers are pollinated by bumblebees, which must force their way through the closed corolla. We would see numerous plants as we traveled around the pond, with most being difficult to access and photograph due to the thick, surrounding vegetation.

Gentiana andrewsii (closed gentian) mature inflorescences.
Gentiana andrewsii (closed gentian) mature inflorescences.

At pond’s edge, we found several examples of Symphyotrichum laterifolium (calico aster), one of the few white fall asters that can be identified fairly easily in the field due to its profusion of smaller-than-average-sized flowers along lateral branches with relatively few rays (9–16) and disc florets turning from pale yellow to purple, lance-elliptic leaves with a “Mohawk” (i.e., hairs only along the midvein) on the underside, and stems covered in soft, white hairs.

Symphyotrichum laterifolium (calico aster).

At the far end of the pond, the group noticed Taxodium distichum (bald cypress) trees (native to southeastern Missouri but not this far north) with strange-looking galls on the twigs. There was some discussion about whether they were caused by an insect or a fungus—their rusty-brown color and numerous spikes brought to mind the galls on Juniperus virginiana (eastern red-cedar) caused by the fungus Gymnosporangium juniperi-virginianae (cedar-apple rust). The fact that both Taxodium and Juniperus are in the family Cupressaceae made the idea of a rust fungus being the culprit seem even more likely. Nevertheless, a little online sleuthing (thank goodness for smart phones!) revealed that the actual culprit was, indeed, and insect—specifically Taxodiomyia cupressiananassa (cypress twig gall midge), a tiny fly. The spongy galls are snow-white at first and then turn brown with age, eventually dropping from the tree as leaves are shed. Maggots pupate inside the galls and adults may emerge from galls that are still on the tree later in the season. Maggots usually overwinter inside fallen galls to pupate and emerge as adults the following spring.

Galls caused by Taxodiomyia cupressiananassa (cypress twig gall midge) on Taxodium distichum (bald cypress).
Galls start out snow-white but turn brown with age.

As we walked, some of the more adventurous among us partook in freshly fallen fruits of Diospyros virginiana (persimmon). Those that were plucked from trees just as they were ready to drop were found to be the tastiest and least stringent, and sucking on the five or so seeds per fruit stretched out the flavor as long as possible. As we enjoyed the impromptu snack, a few still-flowering plants of Bidens aristosa (bearded beggarsticks or tickseed sunflower) were seen near the pond margin.

Bidens aristosa (bearded beggarsticks or tickseed sunflower).
Bidens aristosa (bearded beggarsticks or tickseed sunflower).

Eventually, we spotted from afar a large patch of bright, yellow-flowered composites in the distance. Their brown-purple discs brought the genus Rudbeckia immediately to mind, and our initial thought was R. subtomentosa (sweet coneflower) after seeing some of the large leaves with lobes. Still, the time of bloom seemed very late, and the plants were not as tall nor the leaves as “gray” as would be expected for that species. In reality, the majority of leaves were not lobed, and we decided they instead represented a form of R. fulgida (orange coneflower)—a highly variable and taxonomically difficult complex of populations.

Rudbeckia fulgida (orange coneflower).
Rudbeckia fulgida (orange coneflower).
Rudbeckia fulgida (orange coneflower) involucre.
Rudbeckia fulgida (orange coneflower) leaf.
Rudbeckia fulgida (orange coneflower) stem.

After completing the circuit around Crow Pond, the group caravanned to the northernmost and most recently renovated quarter on the property. Most of the plants established in this large tract of now-tallgrass prairie were well on their way to fall seed (and, in fact, had been combine-harvested for such), but mowing along the gravel access road allowed some still-green regrow the—the most dramatic being Helianthus maximiliani (Maximilian sunflower). This uncommon sunflower is most similar to H. grosseserratus (sawtooth sunflower) due to its large attractive flowers and narrow, curved leaves. However, leaves of the former are grayish due to the presence of many tiny hairs covering the surface of the leaf (in the latter leaves are glabrous), and the stem is rough—also due to the presence of hairs (in the latter the stem is glabrous and has a glaucus coating that can be rubbed off).

Helianthus maximiliani (Maximilian sunflower).
Helianthus maximiliani (Maximilian sunflower) involucre.
Helianthus maximiliani (Maximilian sunflower) stem/leaves.
Helianthus maximiliani (Maximilian sunflower) leaf.

The group agreed that three weeks earlier would have been a good time to see the area, and next spring or summer would be even better!

©️ Ted C. MacRae 2021