Month: April 2023

Snake Road

/ Ted C. MacRae / 2 Comments
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

BitB Bits: March 2023

/ Ted C. MacRae / 2 Comments

Welcome to a new series that I’m calling “BitB Bits,” an irregular collection of random natural history observations recorded in my notes over the previous month. The individual snippets are, by themselves, too short for stand-alone posts, but I hope that readers will find their collective and chronological nature interesting and informative.

March 9. Welcome home walk. Good to be home and glad to see we didn’t miss the start of spring here. Non-native daffodils are blooming everywhere (I must admit they make an impressive display); however, we also have our first native blooming plant—spicebush (Lindera benzoin). Apparently only the male plants are blooming so far (distinguished by their flowers with stamens/anthers only but lacking a central pistil); the female plants should follow suit shortly.

Lindera benzoin (northern spicebush)

March 12. Spring on hold. Now that spicebush is in bloom, a succession of flowering trees and shrubs should follow. Fragrant sumac (Rhus aromatica) would be the next to follow, but the rain of the last few days has put it on hold. The buds are swollen and ready, however, to burst forth on the next sunny day.

Rhus aromatica (fragrant sumac).

March 13. In my happy place. I didn’t get enough hiking at St. Francois State Park to satisfy my desires, so on the way back home I decided to stop off at Victoria Glades, one of my favorite places, and walk the perimeter of the main glade. I don’t think there’s another place on earth where I feel more connected to myself as a naturalist than here. I first visited way back in 1983 – the year after I moved to St. Louis after finishing grad school, and every year for the next eight years I came here once or twice per week throughout the summer to collect insects. I essentially “grew up“ here as an entomologist! In the time since moving back to St. Louis (now 27 years ago), I have resumed my regular visits – more in some years, less in others, and each time I do I feel rejuvenated. I have instructed Madam to sprinkle my ashes here (at least some of them) – if I depart and you happen to read this, please follow up with her to make sure that she does just that!

Victoria Glades Conservation Area, Jefferson Co., Missouri

March 15. Beware the Ides of March. On this day, in 44 B.C., Julius Caesar was stabbed to death by a mob of Roman senators led by his friend Brutus. The senators believed that Julius had consolidated too much power (he had only a year earlier been named dictator for life and was implementing sweeping imperialist offensives in an effort to expand Roman territory), and that his death would lead to the restoration of the Republic. Sadly (or fortunately, depending upon your perspective), the “Ides of March” plunged Rome into centuries of civil war that ultimately led to utter collapse by the 5th century. In the final years of the empire, a series of emperors took the throne in quick succession (usually after the murder of their predecessor by the Praetorian Guard, the emperor’s personal bodyguards), each of whom plundered the state while they had the opportunity. The Roman Senate, engaged in their own corrupt practices and suffering from incompetence, was unable to curb the excesses of these emperors, leading to a waning of civic pride and loss of trust by the Roman citizenry before the final collapse.

March 17. C-c-cold! Once again, the bright sunshine was deceptive, belying how cold it really was – especially with that wind! Temps plummeted even further once the sun set, but the views around my home are still spectacular.

“The pond” on Pond Rd

March 21. Still waiting… …for native blooms to begin. Until then, here is yet another non-native early bloomer—Scilla forbesii (Forbes’ glory-of-the-snow), which invaded the woods near my home after a neighbor planted some in their woodland garden. They are not nearly the problem that some other invasives are (like bush honeysuckle or burning bush) in that they don’t smother out nearby native plants, but they can provide a pollinating “sink” that competes for insects that would otherwise be pollinating the flowers of native plants.

Scilla forbesii (Forbes’ glory-of-the-snow)

March 22. Vernal equiNOT. Spring began two days ago, yet I’m still waiting for the first appearance of any native wildflowers in the neighborhood. Until that happens, here is yet another non-native species—the thankfully noninvasive hyacinth—that my neighbor planted in their garden.

Hyacinthus sp. (hyacinth)

March 24. Spring at last, spring at last, thank God Almighty, spring at last! Finally, after sitting dormant for more than a week, the flowers of Rhus aromatica (fragrant sumac) have opened—in my opinion the true opening salvo of spring. Even so, it’s not like the weather suddenly turned spring-like, but more like the sumacs finally said F this and decided to open despite the continued dreary conditions.

Rhus aromatica (fragrant sumac).

March 25. How do snail’s eyes differ from slug’s? They don’t—they’re both eye tentacles. 🥁

Mesodon thyroidus (white-lipped globe snail)

March 26. Spring beauty. Now that spring is truly here, Claytonia virrginica (spring beauty)—the icon of spring ephemeral wildflowers—has begun popping up everywhere.

Claytonia virrginica (spring beauty)

March 26. Water spider. I saw this large fly sitting on the curb. Of course, I knew it was a crane fly—a member of the family Tipulidae, but I hear people often confuse them for a “giant mosquito.” There is no such thing, and while I admit that they do look superficially like a mosquito on steroids (they happen to be distantly related to mosquitos), they do not bite or suck blood—arguably the most important part about being a mosquito. In fact, crane flies often do not eat anything once they become adults, with some species even lacking functional mouthparts. The family name is derived from the Latin word for “water spider,” perhaps because the larvae live in water and have a ring of tentacles around their head—just guessing. Anyway, I snapped a few pics of the little guy before he feebly began flapping his wings in the chilly air and took flight, probably looking for something to not eat.

Tipula sp. (crane fly)

March 28. Back to winter (midge). A few tantalizingly warm, sunny days had my hopes up that spring was finally here, but the return of cool, wet conditions have brought back that late winter feel. Perhaps appropriately, one of the first insects I’ve seen this season is this small, mosquito-looking fly that is actually a distant relative belonging to a group known as winter midges (genus Diamesa—also called snow midges—in the family Chironomidae). As their common names imply, the adult flies are seen active primarily during winter and can even be seen walking about on snow during warm spells during the winter (a scenario mimicked by the styrofoam on which this individual was photographed). Like the crane flies that I featured a couple days ago, winter midges do not feed as adults—if only for lack of suitable food sources, while the larvae feed on organic debris in cold, running water.

Diamesa sp. (winter midge)

March 29. What’s up, buttercup? Buttercups are popping up in the “more natural“ lawns of my neighborhood. We have a number of species buttercups in Missouri – this one is Ranunculus harveyi (Harvey’s buttercup). In general, you can distinguish buttercups by their small, bright yellow flowers and bristle of anthers surrounding the central disc.

Ranunculus harveyi (Harvey’s buttercup)

March 30. Bloodroot. I made a rather exciting wildflower find in the woodlands around my house this morning—a small patch of Sanguinaria canadensis (bloodroot) with (thus far) but a single bloom. This poppy relative (family Papaveraceae) is so named because of red, fleshy root, which gets its color from alkaloids, chiefly sanguinarine, in its toxic sap. First Americans traditionally used bloodroot to treat fever, rheumatism, ulcers, ringworm, and skin infections, and it is still used to produce natural red, orange, and pink dyes. There is likely some truth to the bioactive properties of bloodroot alkaloids, as they are currently being studied for use as anti-cancer agents, particularly for the treatment of skin cancer, and as a dissolving agent for skin growths such as warts. Bloodroot is also interesting from a natural history standpoint in that the seeds have fleshy appendages that are attractive to ants. The ants collect the seeds and bring them to their nest, thus effecting dispersal of the seeds. This is an advantage for these small plants growing in wooded habitats, where wind speeds are usually too low to aid natural seed dispersal.

Sanguinaria canadensis (bloodroot)

March 31. Sweet William. I saw these plants yesterday while their blooms were still closed and wondered if they would open before March closed out. I normally think of Phlox divaricata (sweet William) as a mid-April bloomer, but clearly it can begin earlier if conditions are right (as they have been the past several days).

Phlox divaricata (sweet William)

©️ Ted C. MacRae 2023

Four for four

/ Ted C. MacRae / 2 Comments

I had a good showing at this year’s WGNSS (Webster Groves Nature Study Society) Photo Contest—held last night at the Webster Groves Public Library. All four photos that I entered—one each in four different categories—were selected for a prize: 1st place in the Invertebrates category, 2nd place in the Bonus category (Missouri Species of Conservation Concern), 3rd place in the Vertebrates category, and Honorable Mention in the Plants and Fungi category. There was a fifth category (Habitats and Landscapes), but I don’t take many landscape photos (at least, not with my “real” camera) so did not submit to that category. Three of the four photos are now eligible (along with 13 others) for the Grand Prize (the bonus category is not included in the grand prize competition), which will be selected via popular vote at the WGNSS Spring Banquet, to be held next month at the Piper Palm House in Tower Grove Park.

1st Place – Invertebrates

The spotted orb weaver (Neoscona crucifera) builds an impressively large web each night, which it consumes in the morning before hiding during the day. Despite their size, they are not aggressive and are of no medical significance. This female was photographed at Pinewoods Lake Recreation Area in Carter Co., Missouri on 11 August 2015.

2nd Place – Bonus (Missouri Species of Conservation Concern)

The swift tiger beetle (Cylindera celeripes) was unknown to occur in Missouri until it was discovered in the critically imperiled loess hilltop prairies of extreme northwestern Missouri in 2010 by Ted MacRae and Chris Brown. The species was designated a Missouri Species of Conservation Concern due to the critically imperiled nature of the habitat in which it lives, and detailed surveys since its discovery in the state have shown the species to be limited to just four loess hilltop prairie remnants – all under conservation management – in Holt and Atchison Counties. This individual was photographed on a sparsely vegetated red clay/gypsum exposure in mixed-shortgrass prairie at Alabaster Caverns State Park in Woodward Co., Oklahoma on 10 June 2009.

3rd Place – Vertebrates

The eastern hognose snake (Heterodon platirhinos) is famous for their variety of defensive behaviors, ranging from the innocuous (puffing their neck and hissing) to the repugnant (vomiting) to the extreme (feigning death). This individual was photographed at Sam A. Baker State Park in Wayne Co., Missouri, on 23 April 2012.

Honorable Mention – Plants & Fungi

The flesh-colored flowers of pawpaw (Asimina triloba) are pollinated by flies more typically attracted to fermenting substances rather than “typical” flower-loving flies seeking pollen and nectar, which they attract by emitting yeasty-smelling fermentation volatiles — rare in floral scent blends.These pawpaw flowers were photographed in mesic forest on an east-facing slope along the lower Wappapello Section of the Ozark Trail in Wayne Co., Missouri on 10 April 2010.

©️ Ted C. MacRae 2023

Day hike at Little Lost Creek Conservation Area

/ Ted C. MacRae / 6 Comments

Today the WGNSS Botany Group visited Little Lost Creek Conservation Area to see Dirca palustris (eastern leatherwood) in bloom. Leatherwood is a distinctive, slow-growing shrub that occurs sporadically in primarily the Ozark and Ozark Border region of Missouri. Like the much more Lindera benzoin (common spicebush), the flowers open in spring before the foliage appears, during which time the planta are easily identified by the pendulous blooms surrounded by wooly bracts. The species has toxic properties and was used by First Americans as an emetic, and it has been cultivated for many years despite its sporadic natural occurrence. As the name implies (palustris means “growing in a swamp”), the plant grows in moist (though not necessarily swampy) habitats, and as such we would have to hike across the dry-mesic upland deciduous forest and down into the riparian forests along Little Lost Creek where the plant can be found.

With sharply warmer temperatures arriving yesterday after a rather protracted cool period, the early-flowering trees and shrubs were ready and waiting, seemingly popping open before our very eyes. A patch of Prunus americana (American plum) in a more open area along the trail caught our attention, it’s blooms just beginning to open. We based our identification on the shrubby growth habit and apparently clonal nature of the stand of plants, which distinguishes P. americana from the closely related P. mexicana (Mexican plum), which generally grows as more tree-like individual plants.

Prunus americana (American plum).

Also in the more open areas along the trail was Rhus aromatica (fragrant sumac) in full bloom. I stopped to examine one particular individual with especially dense clusters of inflorescences and noticed movement on the flowers. Closer examination revealed a crab spider (family Thomisidae) which I took to be Mecaphesa asperata (northern crab spider)—perfectly camouflaged on the bright yellow flowers and awaiting the arrival of an unsuspecting bee or other pollinator.

Mecaphesa asperata (northern crab spider) on on flower of Rhus aromatica (fragrant sumac).

As the trail veered directly into the forest, I noticed several butterfly species—a Vanessa atalanta (red admiral) that paused briefly on the trail before bolting erratically into the distance, several Eurytides marcellus (zebra swallowtail), presumably males patrolling for females among stands of the still leafless Asimina triloba (pawpaw) which it utilizes as a larval host, and—most interesting for me—several Anthocharis midea (falcate orangetip) which, for the time being, frustratingly refused to perch and allow even an attempt at a photograph.

As the trail began the long descent into the valley and the forest became increasingly mesic, spring ephemerals began appearing on the forest floor in abundance. Most abundant was Claytonia virginica (spring beauty) and Cardamine concatenata (cutleaf toothwort), which have been in bloom for some time now, but finally making their appearance as well were Sanguinaria canadensis (bloodroot)—the first seen being a charming little patch nestled against a rock—a single blooming plant among the stands of Erythronium albidum (white trout lily), and several still-unblooming Trillium sp. (wakerobin).

Sanguinaria canadensis (bloodroot).
Erythronium albidum (white trout lily).
Trillium sp. (wakerobin).

At last we reached the valley floor, and immediately the leatherwood plants were seen in abundance and in full bloom. Leatherwood plants in bloom are not among the showiest of blooming shrubs, but the distinctiveness of their flowers, sporadic occurrence, and lack of close relatives provided ample botanical interest that resulted in me spending a fair bit of time observing and photographing them.

Dirca palustris (eastern leatherwood).
Dirca palustris (eastern leatherwood).

As I looked at the leatherhood, I encountered a an unusual cocoon-like structure at the tip of one of its branches. Closer examination revealed it to be “packed” white tiny, white, grub-like larvae, at which time I noticed the cadaver of a moth caterpillar also clinging to the branch tip. I knew then that the grubs were the mature larvae of a parasitic wasp in the family Braconidae, likely in the subfamily Microgastrinae, that had just exited their host and were spinning cocoons nearby in communal fashion. (Many people have seen one of these wasps in the form of cocoons on the backs of tomato hornworm caterpillars.) Braconid wasps are often quite host specific, but a more specific identification is difficult since the identity of the caterpillar itself or whether it was utilizing Dirca as a host plant are also unknown.

Braconid larvae, possibly subfamily Microgastrinae, spinning communal cocoons after exiting unidentified lepidopteran caterpillar on Dirca palustris.

If the spring ephemerals were abundant during the descent, they were overwhelming in the valley proper. A few blooming plants of Collinsia verna (blue-eyed Mary), a winter annual were seen, their distinctive bicolored white and blue flowers a pleasant contrast to the mostly white to pinkish color of the majority of the ephemerals. Some especially large-flowered individuals of bloodroot were seen underneath a patch of blooming leatherwoods, prompting me to spend a bit more time photographing them. As I was doing so, I found it ironically humorous that I was crouched on the ground photographing what is by all measures a rather common plant while surrounded by a much less frequently encountered plant.

Collinsia verna (blue-eyed Mary).
Sanguinaria canadensis (bloodroot).
Sanguinaria canadensis (bloodroot).

The hike back up out of the valley was long and deliberate, the pitch in some stretches reaching as steep as I ever encounter on trails in the state, but the slow pace allowed an opportunity to look for things missed on the way down. At one point I picked up a fallen oak branch that looked like it might have been pruned by a twig pruner (Anelaphus sp.), a type of longhorned beetle (family Cerambycidae) whose larvae feed within living branches of deciduous trees—primarily oak—and then cut the branch internally before pupation. The cut end is distinctive, and I checked the base of the branch to see if it demonstrated this distinctive cut pattern. It did not, but I explained what I was looking for to a curious member of our group. Just as I finished the explanation, I saw another oak branch laying on the trail, picked it up to examine the base, and, sure enough, it exhibited the cut. I believe the branch is that of black oak (Quercus velutina), and I kept the branch to place within a rearing box so I can see the adult when it emerges later this spring.

Along the final stretch back to the parking lot, the falcate orangetip butterflies continued to torment me with their erratic, never-ending flight. I watched a few after reaching the parking lot, hoping one would alight and give a chance to photograph it, but no such luck. At the edge of the parking lot I noticed some Taraxacum sp. (dandelion) flowers with small insects on them, which turned out to be Acmaeodera tubulus—usually the first jewel beetles (family Buprestidae) to appear in the spring and commonly found on dandelions. I crouched to take a few photographs, and as I was doing so a falcate orangetip butterfly landed on the dandelion flower right next to the one with the beetles I was photographing. I managed to get one shot of the butterfly, it’s wings not well spread out but the orange tips still easily visible, before it took flight again—a nice punctuation to end the outing with.

Acmaeodera tubulus on on flower of Taraxacum sp. (dandelion).
Anthocharis midea (falcate orangetip) on flower of Taraxacum sp. (dandelion).

©️ Ted C. MacRae 2023