Tag: Ithaca

Discovering Large-Flowered Bellwort Near Mundy Wildflower Garden in Ithaca, New York

On an April afternoon along Fall Creek near Cornell Botanic Gardens, I found my first colony of Large-flowered Bellwort, Uvularia grandiflora—a quiet woodland wildflower shaped by spring light, pollinators, and rich forest soil.

MichaelStephenWills7 Comments

On an April afternoon in 2026, walking along Fall Creek near the Mundy Wildflower Garden at Cornell Botanic Gardens, I came for the first time upon a colony of Large-flowered Bellwort, Uvularia grandiflora, and stopped with the immediate feeling that spring had spoken in a new dialect. I had seen the season gathering itself all around me in buds, in damp leaf litter, in the first loosening of the woods from winter’s gray restraint. But this was different. These flowers did not announce themselves with bravado. They hung quietly beneath their leaves, as though the forest had shaped small yellow lanterns and then thought better of showing them too openly.

I raised my Canon EOS 5D Mark IV with the Canon EF 100 mm f/2.8 Macro USM lens and photographed them handheld at 1/640 second, f/8.0, trying to honor both their delicacy and their poise. Macro work often feels like an act of courtship with detail. One does not seize the subject; one approaches, waits, adjusts, breathes. In the bellworts, I found a plant that rewarded just this kind of attention. At first glance they seemed merely graceful. Then, looking more closely, I began to see their architecture.

These Largeflower Bellworts (Uvularia grandflora) are flourishing on the Cornell University Campus along Fall Creek, adjacent to the Mundy Wildflower Garden. Cornell University, Tompkins County, finger Lakes Region, New York State

Large-flowered Bellwort is a woodland perennial of rich deciduous forests, and it wears that identity in every part of its form. The stems rise smooth and pale, slender but assured, each seeming to carry its burden effortlessly. The leaves clasp the stem in that distinctive bellwort manner, as though the plant were being held in green hands. Beneath them hang the flowers, elongated and drooping, their six yellow tepals twisted and tapered into points. They are not the symmetrical stars of more open-faced blossoms. They are pendants, streamers, tassels of sunlight. In these flowers, yellow becomes motion. Even when still, they seem to trail the memory of a breeze.

The plant’s drooping habit is part of an evolutionary strategy. In the spring woods, before the canopy fully leafs out, ephemeral light reaches the forest floor in a brief annual inheritance. Bellwort rises into that window. It gathers energy quickly, blooms early, and makes use of the few bright weeks before the trees above turn the woodland dim and green. Its season is a narrow one, but not a meager one. This is a plant shaped by timing, by patience, by fidelity to a recurring opportunity. It lives where sunlight is not constant but bestowed.

There is something deeply moving in such an existence. We humans often admire the grand gestures of nature—the waterfall, the hawk, the thunderhead. But woodland wildflowers teach another lesson: that persistence may take the form of exquisite brevity. Uvularia grandiflora does not dominate the landscape. It waits for its rightful hour, then enters the year with quiet authority. It is one of spring’s soft-spoken triumphs.

Ecologically, the bellwort belongs to a community rather than a spectacle. It grows in moist, humus-rich soil, among the remains of last year’s leaves, where decay has become nourishment. Around it are the signatures of a healthy eastern woodland: filtered light, fungal work below ground, the gradual release of nutrients from the forest’s own past. Its roots do not stand apart from this economy of return. They participate in it. The beauty of the flower is inseparable from the labor of decomposition, the unseen commerce of roots and microbes, the long winter’s accumulation of leaf mold. Even here, elegance rises from compost.

And then there are its relationships with other living things. The flowers, nodding and somewhat enclosed, invite a certain intimacy from insect visitors. Bellwort is not a billboard flower. It asks a pollinator to come close, to enter its hanging chamber. Bumblebees, mason bees in the genus Osmia, sweat bees in Halictus and Lasioglossum, and mining bees in Andrena are among its visitors. One bee, Andrena uvulariae, bears in its very name the mark of this botanical relationship, having evolved a close association with Uvularia. To stand before these flowers is to imagine that hidden commerce of spring proceeding just beyond the edge of one’s notice: a queen bumblebee nosing into a drooping bloom, a small Osmia working deliberately among the tepals, an Andrena bee moving with ancient purpose through a plant lineage it has learned by evolution to trust.

What we call a wildflower is also an agreement, a contract written between blossom and insect long before we arrived to admire it. Even after flowering, the bellwort participates in the forest. Its seeds bear fleshy appendages that attract ants, which help carry them away and disperse them through the woodland.

Human beings, of course, enter this world differently. We bring names, lenses, curiosity, memory. We kneel in leaf litter with cameras. We identify, compare, and sometimes misidentify. We make gardens to protect what once grew without us, and then discover that our finest role is not mastery but attention. Finding Large-flowered Bellwort near Fall Creek reminded me that our relationship to such plants is at its best when it is grounded in humility. We do not improve these flowers by naming them; we improve ourselves by learning to see them.

And seeing them, truly seeing them, is no small thing. The petals in these photographs are veined with light. The stems carry a woodland grace, as if drawn in one uninterrupted line. The colony as a whole had the look of a little parliament of bells, each one bowed, each one speaking in silence. They seemed to me like fragments of sun that had slipped through the trees and decided to remain rooted there.

I left Fall Creek that afternoon with the feeling that I had been admitted to a finer scale of perception. Large-flowered Bellwort asks little of the passerby except slowness. Yet in return it offers a great deal: form, adaptation, timing, kinship, restraint. It shows how life in the spring woods is built from tact. Not only from survival, but from style.

Some plants shout the season into being. Bellwort lets it ring softly. And once heard, that note stays with you.

Enter your email to receive notification of future postings. I will not sell or share your email address.

Stones That Traveled: Glacial Erratics, Deep Time, and the Stories They Leave Behind

Glacial erratics are immigrant stones—carried south by ice, dropped without explanation, and left behind to challenge our sense of permanence, place, and deep time.

MichaelStephenWills22 Comments

There are rocks that merely sit where gravity has placed them, and then there are rocks that arrive with stories already embedded—foreign syllables carried south on ice, dropped without explanation, and left for us to puzzle over. Glacial erratics belong to the second category. They are migrants with no passports, refugees of deep time, whose presence quietly contradicts the landscape that hosts them.

Long before anyone reached for a hand lens or an ice-flow diagram, people answered such contradictions with imagination. In Ireland, a boulder perched just so on a mountain side is not a geologic problem but a resting place. Leprechauns, we are told, favor such stones—high enough to observe human intrusion, solid enough to outlast it. Skepticism, as folklore reminds us, is not always a stable position. Kevin Woods—better known as McCoillte—found that out the hard way when doubt collided with experience on the slopes of Slieve Foye. What followed was not merely a conversion story, but an act of modern mythmaking: folklore translated into bureaucracy, imagination petitioning regulation, and “The Last Leprechauns” entering the unlikely language of conservation. Stone, story, and belief hardened together into something oddly durable.

Rocks such as this are a favorite perch for leprechauns to rest and contemplate the works of man who have invaded their world. Inhabitants of Carlingford who wander Slieve Foye have come upon them often enough, their stories and certitude in the existence of the Little People are resistant to manifold doubters with their reasons and arguments. Kevin Woods, aka McCoillte, was a doubter until worked on a stone wall on property he owned on Ghan Road, Carlingford. His belief did not arise on the discovery of the leather purse, covered with ages of dust and lime, nor with the gold coins inside. McCoillte pocketed the coins for luck. As luck would have it, McCoillte loved to walk on Slieve Foye. It was on one such walk he and his dog encountered Little People who paralyzed them to escape. His unexplained absence led to troubles with the wife. This experience brought McCoillte around to enough of a belief that he, with lots of help, succeeded in petitioning the E.U. European Habitats directive to recognize leprechauns a protected species. A reserve was establish on Slieve Foye to protect the “Last Leprechauns” and you can google this phrase to learn more about McCoillte’s stories.

Back in the Finger Lakes, we tend to use a different grammar when confronted by an out-of-place rock. We name it, classify it, and trace its lineage northward. Erratics scattered across Tompkins County are geological sentences that begin somewhere else entirely. The bedrock beneath Ithaca—Devonian shale and sandstone—cannot account for crystalline intruders left behind like forgotten punctuation marks. These stones speak of ice sheets thick enough to erase valleys and decisive enough to transport mountains in fragments.

Some of those fragments have been domesticated. Cornell, for example, has never been shy about rearranging its stones. An unremarked erratic along the Allen Trail may once have been shrugged off as inconvenient rubble, while another—dragged from the Sixmile Creek valley—was carved into a seat and made eloquent. The Tarr memorial boulder, resting near McGraw Hall, transforms erratic stone into deliberate monument. It invites rest, contemplation, and perhaps gratitude for those who taught us how to read landscapes written by glaciers.

We find boulders of crystalline rock, commonly derived from Adirondack sources, left behind on the surface of ablation moraine, in the Finger Lakes Region. Cornell finds some and move them, maybe the case for this unremarked erratic found along the Allen Trail of FR Newman Arboretum. Another enormous erratic, brought in from the Sixmile Creek valley, was carved into a seat as a memorial to Professor R.S. Tarr who deciphered much of the glacial history of the Finger Lakes Region. Find it at the southwest corner of McCraw Hall on the Cornell University Campus. Reference: “The Finger Lakes Region: Its Origin and Nature,” O.D. von Engeln, Cornell University Press, 1961 page 106

Glacial Erratic, Fillmore Glen

Elsewhere, erratics remain defiantly themselves. In winter, one along Fall Creek alternates between anonymity and revelation, depending on whether snow smooths its surface or retreats to expose lichen constellations. Bridges pass overhead, traffic flows, semesters turn over, yet the rock remains unimpressed. It has already endured pressure sufficient to rearrange its crystals; a passing academic calendar is not likely to trouble it.

Glacial erratic with and without a snow covver and spotted by lichen along Fall Creek in a winter afternoon as seen from Cornell Botanic Gardens. That is the bridge over Fall Creek on Forest Home Drive. Cornell University, Ithaca, Tompkins County, New York State

Closeup of the same boulder

This boulder, a glacial erratic, was found near Fall Creek and the Cornell Botanic Gardens Horticulture Building. Cornell University, Ithaca, Tompkins County, New York State

This rock, a glacial erratic, was found near Fall Creek and the Cornell Botanic Gardens Horticulture Building. Cornell University, Ithaca, Tompkins County, New York State

Then there are the stones that confront us most directly—those we stumble upon in fields, pulled from soil by plow or frost, demanding explanation. A white, iron-stained marble boulder in a Tompkins County field is not subtle about its foreignness. It does not belong to the local vocabulary of shale and sandstone. Its pale surface, crystalline texture, and mineral scars point insistently north, toward the Grenville terrane of the Adirondack Lowlands. The Balmat–Edwards–Gouverneur marble belt offers the most persuasive origin story: metamorphosed carbonate rock carried south by Laurentide ice, released when climate and physics finally lost patience with one another.

I found this white marble erratic in a Tompkins County field. The highest-probability source is Grenville marble from the NW Adirondack Lowlands / St. Lawrence County (Gouverneur/Balmat–Edwards marble belt), delivered by southward-flowing Laurentide ice. I say the most probable source is metamorphosed carbonate (marble) from the Grenville terrane to the north—especially the northwest Adirondack Lowlands / St. Lawrence County marble belt (the “Gouverneur Marble” and related Grenville marbles), transported south by the last Laurentide ice sheet. Why that’s the best bet: Ice-flow geometry favors a northern source. In the Finger Lakes, glacial ice advanced with a flow direction that was very close to due south, guided by the north–south bedrock valleys. Tompkins County erratics are “exotic” imports. Local bedrock around Ithaca/Tompkins is Devonian shale/sandstone, but the region contains many nonlocal (“exotic”) glacial erratics carried in from much farther north (including southern Canada and beyond). Marble isn’t local to the Ithaca area, but it is abundant in the NW Adirondack Lowlands. The Balmat–Edwards/Gouverneur area in St. Lawrence County is a classic Grenville Lowlands district with marble belts (the same province that yields cream/white building marble around Gouverneur).

What makes this particular erratic compelling is not just its provenance, but the improbability of its journey. Ice moved with purpose here, flowing south along bedrock valleys like Fall Creek and Cayuga troughs, turning the Finger Lakes region into a conveyor belt for distant geology. When the ice melted, it left behind evidence that refuses to blend in. Erratics are geological truth-tellers. They announce that this place was once unrecognizable, that what seems permanent is merely provisional.

Perhaps that is why folklore clings so naturally to stone. Whether leprechauns or Laurentide ice are credited, erratics insist on a larger frame of reference. They ask us to imagine landscapes in motion and beliefs under revision. A boulder can be a seat, a marker, a perch, or a puzzle—but never merely background. It waits, quietly confident, for us to catch up to its story.

Enter your email to receive notification of future postings. I will not sell or share your email address.

Atkinson Hall and the Quiet Confidence of Good Design

A new Cornell building settles into its hillside, glass and weathered metal catching sky and trees—less a declaration than an invitation to pause, wander, and think together.

MichaelStephenWills10 Comments

Learning the Shape of a New Building

I first noticed the building from above.

Not in person—on my screen, late at night, when I should have been revising a draft and instead opened Google Earth the way some people open a window. There it was, just off Tower Road, close to Stocking Hall, pale and newly settled into the slope. From that height it looked careful rather than confident, as if it had arrived recently and was still deciding how much of itself to show.

Atkinson Hall, Google Earth from August 2023, 350 Tower Rd, Ithaca, NY 14850

I remember thinking: good placement on a former triangular parking lot. Enough distance from the older buildings to breathe, close enough to feel included. The hill does most of the work. You can see that even from an overhead height.

The next morning I walked there.

Atkinson Hall as viewed from the open field south of the Nevin Welcome Center of Cornell Botanic Gardens

Across the open field the building didn’t announce itself. Trees intervened—pines, bare hardwoods—so that it came into view in pieces: a curve of metal, a long line of glass, brick holding the ground. It felt less like approaching a destination than like gradually realizing you were already there. I liked that. Buildings that reveal themselves all at once tend to exhaust me.

The slope matters. You feel it in your legs as you walk, and the building seems to acknowledge it, stretching rather than standing tall. It does not pretend the land is flat. It follows the descent toward the creek, toward the older geological story underneath all of us.

Up close, the materials settle my attention.

North Side of Atkinson Hall, 350 Tower Rd, Ithaca, NY 14850

Brick at the base—solid, Cornell-familiar, not trying to reinvent anything. Above it, bands of weathered metal curve gently, already carrying the muted browns of fallen leaves, old stone, and stream-worn shale—colors long familiar to the slopes and ravines that shape this campus. They look as though they have agreed to age, which feels like an underrated design choice. The glass holds the sky without insisting on transparency. Some days it reflects trees so clearly that the building nearly disappears into them.

Compare the facade brickwork of Warren Hall, one of the earliest buildings on the Cornell University campus, completed 1868. This is the southwest corner with facade signage, Cornell University, Ithaca, New York

I stop near the windows longer than I intend to. The view steadies me. The hillside, the trees, the quiet persistence of winter light. My notebook stays closed for a few minutes. No one seems to mind.

View near Atkinson, Nevin Welcome Center, Cornell Botanical Gardens, 124 Comstock Knoll Dr, Ithaca, NY 14850

Inside, the building does not behave like a department.

That is the first thing I notice once I begin using it regularly. No single discipline claims the space. Offices and meeting rooms feel provisional, lightly held. Conversations drift. Someone from engineering crosses paths with someone from policy. A food systems researcher borrows a chair from a planner. No one looks lost.

It helps to remember who gathers here. The building hosts people from many parts of the university, each arriving with partial expertise, incomplete questions.

Cornell College / UnitAreas of Engagement
College of Agriculture and Life Sciences (CALS)Food systems, agroecology, climate resilience
College of EngineeringEnergy systems, materials, infrastructure
College of Arts and SciencesEarth systems, ecology, human dimensions
SC Johnson College of BusinessSustainable enterprise, supply chains
College of Architecture, Art, and Planning (AAP)Urban resilience, adaptive design
Cornell Law SchoolEnvironmental law and governance
Public & Global AffairsClimate policy, diplomacy

I keep this list taped inside my notebook. It reminds me that no one here is meant to arrive fully formed. The building expects us to be unfinished.

Cobblestones with fallen oak leaves along Feeny Way, Cornell University, Ithaca, New York

There is a quiet confidence in how the place is run. Systems hum discreetly. Heat holds steady even when the weather rips. Somewhere nearby, unseen, a generator waits, a reassurance. Work continues. Conversations do not end mid-sentence. I think about this more than I expected to. Stability has become a form of generosity.

On certain afternoons I walk the exterior again before heading home.

The curves soften what could have been institutional. Corners ease into one another. Nothing feels sharp. The building does not posture or instruct. It listens. It seems content to let weather, foot traffic, and time finish the job.

I have overheard visitors describe it as “restrained.” I think that is right. It does not wear sustainability as an emblem. It does not ask to be admired. It offers something quieter: space to think without being hurried, to talk without being territorial.

From some angles it nearly disappears into the hillside. From others it asserts itself just enough to be useful. That balance feels intentional, and also rare.

When I sit near the glass and look out, I sometimes imagine the building learning us in return—our habits, our pauses, the way we linger in doorways when a conversation matters. It seems designed for that kind of noticing.

If I were forced to describe it the way a realtor might, I would say it is well built in all the ways that matter. The structure is sound. The site is excellent. The materials will age well. But what I would mean is something less technical.

It is a building willing to wait.

Seen from above, it is still new.
Seen from the field, it is already settled.
Seen from inside, it feels patient.

That patience makes room—for uncertainty, for collaboration, for the long work that does not resolve quickly. I think that is why I keep returning, even on days when I do not strictly need to be there.

The building does not ask what I am producing.
It asks only that I stay awhile.

And for now, that is enough.

Enter your email to receive notification of future postings. I will not sell or share your email address.

Exploring Malloryville Preserve: A Hidden Glacial Wetland Gem in New York’s Finger Lakes

Explore the O.D. von Engeln Preserve at Malloryville, a hidden Finger Lakes wetland where glacial eskers, kettles, and springs reveal the deep story of ice and water.

MichaelStephenWills20 Comments

In the heart of upstate New York, the Finger Lakes region stretches out like a handprint left by the last great ice sheets—long, narrow lakes aligned north to south, their steep-sided valleys feeding into a lattice of creeks, waterfalls, and wetlands. It is a landscape defined by water and time: glaciers grinding south, then melting back north some 12,000 years ago, carving deep troughs, piling up ridges of gravel and sand, and leaving behind a terrain that is anything but simple.

The O.D. von Engeln Preserve at Malloryville, near the small village of Freeville, is one of the quiet places where that story is written most clearly on the land. It doesn’t shout like Taughannock Falls or Ithaca’s famous gorges. Instead, it whispers—through the curves of its hills, the softness of its ground, the unexpected appearance of a spring at the base of a gravel ridge. Here, in a relatively compact area, you can see how ice and water worked together to shape the Finger Lakes region we know today.

Overflow from a Kettle Pond threads through a meadow before feeding Fall Creek. The O.D.von Engeln Preserve at Malloryville.

By the time the preserve officially opened in 1997, the name O.D. von Engeln was already familiar to anyone curious about local geology. His classic book on the Finger Lakes helped generations of readers understand that the scenery around them was not random, but the result of powerful, understandable processes. Reading von Engeln, the rolling hills and quiet valleys near Freeville become more than background—they become evidence: of buried ice, rushing meltwater, and the slow settling of sediments into the forms we walk on now.

Malloryville is an outdoor classroom for that lesson. The preserve is built around a cluster of glacial landforms—eskers, kames, and kettles—that create a three-dimensional mosaic of ridges and hollows. Eskers, those long, winding gravel ridges left by rivers that once flowed inside the glacier, snake through the forest like frozen currents of stone. Kames—steep, irregular hills of sand and gravel—rise suddenly from the surrounding lowlands. Kettles, the depressions left behind when buried ice blocks melted away, now cradle wetlands and pools.

Beneath and between these features, groundwater is constantly on the move. It seeps through layers of sand and gravel, emerges as cold springs at the foot of slopes, and spreads out into swamps, fens, and marshes. In the Finger Lakes, water is always telling a story; at Malloryville, it’s simply easier to hear. Follow the trail and you move through a succession of wet worlds: a seep-fed fen with delicate mosses and sedges, a shrub swamp where skunk cabbage thrusts up in early spring, a cattail marsh that hums with birds and insects in summer.

For my family, the story of Malloryville began even before the preserve had a name. We lived nearby along Fall Creek, itself a thread in the larger fabric of the Cayuga Lake watershed. My son and I camped for the first time on top of an esker just beyond our front door, our tent perched on what I would later learn was the remnant of a stream that once tunneled through the base of a glacier. At the time, it was simply a magical narrow ridge in the woods. Only later, with von Engeln’s guidance and the preserve’s interpretive signs, did that ridge become a sentence in a much older, longer narrative.

That is one of the great gifts of the Finger Lakes: the chance to move from simple admiration—“this is beautiful”—to understanding—“this is how it came to be.” The steep slopes along Cayuga, Seneca, or Skaneateles; the drumlin fields near the north ends of the lakes; the hanging valleys and waterfalls; and the quiet wetlands of places like Malloryville are all chapters in the same glacial chronicle. Once you learn to read one place, you begin to read them all.

Walking into the O.D. von Engeln Preserve, you enter that story at a small, intimate scale. The parking area and trailhead give way quickly to a world where the ground feels different—sometimes firm and gravelly, sometimes soft and yielding underfoot. Wooden walkways and narrow paths thread through shady forest and open wetland. Each bend offers a subtle shift: a new plant community, a change in water clarity or flow, a small sign explaining what lies beneath your feet.

Fall Creek meanders through the esker fields of the Malloryville Preserve. Here is the view from an abandoned railroad bridge. The preserve is near Freeville in the Finger Lakes Region of New York State.

This is not grand scenery in the postcard sense; it is something quieter and deeper. Malloryville invites you to slow down and notice. To ask why a particular ridge is so narrow, why water emerges here but not there, why one hollow is filled with shrubs and another with moss and sedge. In learning those answers, you gain not only an appreciation for this modest preserve but also a richer understanding of the entire Finger Lakes region.

The Trout Lily (Erythronium americanum) is named for the mottled brown leaves resembling marking on trout.

In the end, the O.D. von Engeln Preserve at Malloryville is a lens—a way of seeing. Through it, the familiar landscapes of central New York—valleys, hills, streams, and lakes—come into sharper focus as the lasting work of ice and water. Stand on an esker, look across a kettle wetland, listen to the quiet trickle of a spring, and you are standing inside the very processes that shaped the Finger Lakes.

Enter your email to receive notification of future postings. I will not sell or share your email address.

The Mathematical Beauty of Autumn Leaves

Here I reflect on the mathematical beauty of falling leaves from two trees, revealing order amidst perceived chaos in nature’s patterns.

MichaelStephenWills17 Comments

Standing before these two trees on a unseasonably warm autumn day, I am struck by the intricate patterns of their fallen leaves. Against the vibrant green of the grass, the golden leaves form halos around the trunks, as if nature herself were sketching mandalas. There’s something profoundly mathematical about these arrangements—a quiet order amidst what might initially seem like chaos.

The first tree, its barren branches reaching skyward, stands on a carpet of yellow that radiates outward in near-perfect symmetry. The leaves have fallen in such a way that their density decreases as the distance from the trunk increases. It reminds me of the inverse square law—a principle in physics that governs how light, gravity, and sound diminish with distance. Here, instead of energy dispersing, it’s the leaves thinning out, their graceful scatter dictated by the wind’s whims and gravity’s pull. There’s an undeniable harmony in this seemingly random process, a convergence of natural forces creating an elegant gradient.

Stewart Park, Ithaca, New York

The second tree presents a different story, yet one equally mesmerizing. Its leaves, still clinging in part to the branches, form a looser ring at the base. The distribution is uneven, hinting at prevailing winds or the sheltering influence of nearby buildings. But even in this asymmetry, I see fractals—the self-similar patterns that repeat at different scales throughout nature. Look closely, and you’ll notice clusters of leaves mimicking the broader structure of the canopy above. It’s as if the tree’s essence is echoed in the ground below, a reminder of how deeply interconnected every part of a system can be.

Robinia pseudoacacia, commonly known as the black locust

These patterns invite reflection on the mathematical principles governing our world. Fibonacci sequences, golden ratios, and fractals—abstract concepts are not confined to textbooks. They are etched into the fabric of existence, visible in the spiral of a sunflower’s seeds, the curve of a nautilus shell, and the fall of leaves beneath a tree. Even the chaos of autumn is underpinned by order, a dance choreographed by countless variables: the angle of the branches, the strength of the wind, the moisture in the air.

I find myself wondering about the unseen forces at play. How many leaves fell straight down, obeying only gravity? How many were carried aloft by a breeze before settling farther afield? Could we model these patterns with algorithms, tracing the arc of each leaf’s descent? Would the data reveal a perfect equation, or would it remind us that some mysteries resist full comprehension?

As I stand here, I feel a deep gratitude for these natural equations. They ground me in the present moment while also connecting me to the infinite. The pattern of leaf fall is a reminder of life’s balance: chaos and order, randomness and structure, fleeting moments and timeless principles. The trees, now shedding their golden crowns, invite me to pause, observe, and marvel at the beautiful mathematics of autumn.

Enter your email to receive notification of future postings. I will not sell or share your email address.

Autumn Reflections: The Majesty of Acer Rubrum

On a serene autumn afternoon by Beebe Lake, a solitary red maple stood out against the backdrop, showcasing its vibrant colors and resilience, symbolizing autumn’s fleeting beauty.

MichaelStephenWills25 Comments

It was one of those serene autumn afternoons that linger in memory, the kind where the sky seems impossibly clear, the air crisp and gently scented with fallen leaves. I stood at the edge of Beebe Lake, my gaze first drawn to the textured concrete dam holding back the water, its weathered facade contrasting sharply with the soft reflections shimmering across the lake’s calm surface. Beyond, the wooded hillside rose gently, a tapestry woven with the warm hues of autumn—golds, greens, oranges, and reds mingling like brush strokes on a canvas.


An October Glory, turning before all others

Yet amidst this collective beauty, one tree captured my attention, singular in its brilliance—a solitary red maple standing proudly on the lakeshore. Its leaves had turned a vivid crimson, blazing brightly as though defying the muted earth tones surrounding it. Even from a distance, framed and partially obscured by larger trees, its vibrant reflection cast a fiery echo on the water, rippling softly in the afternoon breeze.

The maple, Acer Rubrum, seemed perfectly at home here, thriving robustly at the water’s edge. I remembered reading how adaptable red maples are, able to flourish in conditions ranging from dry uplands to swampy shores. This spot, near the edge of the tranquil Beebe Lake, seemed to showcase its resilient character perfectly.

Up close, the maple’s glow was even more striking. Its leaves cascaded in fiery clusters, hues deepening from bright scarlet at the tips to a darker maroon closer to the branches. This dramatic gradient seemed symbolic of autumn itself—beautiful, fleeting, and subtly tinged with the melancholy reminder of winter’s approach.

The Red Maple (Acer Rubrum) to tolerant of diverse conditions, making it a perfect choice for this spot on the short of Beebe Lake.

A memory surfaced of early spring in the Finger Lakes region, a time when maples, including this red maple, generously share their sap. Though not traditionally tapped like its sweeter cousin, the sugar maple, this species’ sap can indeed be boiled down into syrup, a surprising sweetness hidden within its sturdy trunk. Standing in its shadow, imagining those early spring days, it seemed astonishing that the same tree could offer both the delicate sweetness of syrup and the fierce beauty now on display.

Curiously, the transformation of the tree appeared methodical yet whimsical—it changed colors from the top down, its upper branches already bare, exposing slender twigs pointing skyward. Like an artist carefully removing layers to reveal something deeper beneath, the maple unveiled its upper bare bones first, as though reminding observers of the quiet strength supporting its autumn splendor.

This Red Maple (Acer Rubrum) turns from the top down and has already bare for most top branches.

As I lingered, taking in this turning tree, joggers passed by along the path, their rhythmic footsteps a gentle percussion beneath the rustling leaves. Briefly, they glanced toward the vivid maple, perhaps drawn, like me, by its striking contrast to the surrounding foliage. It felt like we shared a secret admiration for this singular tree, recognizing in it a quiet assertion of individuality amidst conformity.

Eventually, I viewed the maple once more from afar, framed now by broader sweeps of branches and leaves, partially obscured but no less vivid. Through layers of leaves and dappled sunlight, it glowed like a distant flame, a beacon that seemed to encapsulate the entire mood of the season—warm yet cool, bright yet transient.

The Red Maple (Acer Rubrum) is the first to flower in spring and the first to turn in autumn.

Walking away, the image of that maple lingered, its reflection shimmering gently in the afternoon sun, a moment suspended between summer’s lush vitality and winter’s bare stillness. Beebe Lake had offered scenic beauty, a quiet meditation, a reflection mirrored not only on its tranquil surface but in the heart of an observer captivated by a single tree’s fleeting glory.

Enter your email to receive notification of future postings. I will not sell or share your email address.

Monarch Butterfly Life Cycle: Egg to Adult (Danaus plexippus) with Photos

From milkweed egg to striped caterpillar, jade chrysalis, and fluttering monarch, witness metamorphosis, migration, and our role in protecting Danaus plexippus across North America today.

MichaelStephenWills17 Comments

On the underside of a milkweed leaf, the world begins small enough to miss unless you kneel and look closely. In this first photograph the newborn is still a whisper of life, a pale pinhead egg collapsed into a glistening scrap, the tiny caterpillar beside it like a gray comma punctuating the green. It has just eaten the soft shell that cradled it—its first meal, its first thrift. The leaf’s pale roads of veins radiate around the hatchling; within that simple map lies all the geography it needs.

By the second photograph appetite has taken its proper throne. These pilgrims wear a uniform of warning: bands of yellow, black, and white—stripes as bright as hazard tape, a heraldic banner advertising the bitterness borrowed from milkweed. Each bite draws down defensive latex; yet the caterpillars feed undeterred, pausing to snip the leaf’s veins to quiet the flow. Their black, threadlike “tentacles” nod as they travel, and their peppery pellets—frass—collect like midnight hail. Five times they will outgrow themselves, shrugging off skins to reveal wider, hungrier versions within. The room is strewn with green rib and ragged edges; the air has the gentle smell of cut stems. All the while, milkweed’s poisons, the cardenolides, pass into growing bodies and become their bodyguard.

At last a hush. A final meal, a purposeful wander. The caterpillar chooses a high eave of the world—a stem, a stick, the corner of your rearing tent—and hooks itself into a downward J. Within hours the skin splits like a soft zipper; the striped creature pours itself out of itself and seals into a smooth chrysalis.

Here, the caterpillar has attached itself to a silk pad from which it hangs. Underneath the skin, the caterpillar is transforming to the chrysalis. In these photographs the silk pad and chrysalis attachment from a previous transformation are in the foreground.
Macro of the Monarch butterfly chrysalis. The black stalk attached to the silk pad is call a cremaster.

The following photograph and video catch the moments into becoming: the jade lantern has become transparent, darkening, its gold studs glinting like constellation points, and through the thinning walls the folded wings show, orange smoldering under smoke. Inside, old tissues have dissolved into a living broth; imaginal discs—tiny blueprints carried since the egg—have flowered into legs, eyes, and flight. To call it “metamorphosis” is correct; to call it mystery is truer.

Watch on YouTube for a better experience. Please “like” and “subscribe”

When the case opens the butterfly backs into the bright. It clings while the crumpled wings fill and flatten, hemolymph pumping life into every cell. In the next image the adult drinks from a petunia trumpet, a jeweled ember with white-spotted hems. The monarch—Danaus plexippus—tests the wind with new, purposeful wings. Its scientific name nods to ancient stories: Danaus after the Greek mythic king of Argos, a father who fled with his fifty daughters across the sea; plexippus for Plexippus, a figure of the same old tales—his name carried forward into this wanderer of the sky. The English name “monarch” is said to honor both its regal size and domain, and, some say, the orange-and-black of William of Orange. Kings and myths gathered like cloak and scepter around a creature that weighs less than a paperclip.

No butterfly has entered human life more completely. Schoolchildren cradle jars of milkweed sprigs and tape handwritten labels to chrysalides lined like seed pearls along a classroom window. Taggers kneel in September light, add a tiny disc to a wing, and write down time and place so the journey south can be traced. In the mountains of Mexico, where oyamel firs hold winter like a secret, people fold the monarch’s return into the Days of the Dead, believing that souls ride home on those wafers of flame. Gardeners tuck swamp milkweed into narrow beds and call their yards “waystations.” Photographers, such as myself, record the stories that happen leaf by leaf.

In early July a Monarch caterpillar revels in milkweed flowers.

Yet our touch is not simple. Fields simplified by herbicides have shaved milkweed from fencerows; tidy mowing removes nectar from roadsides in the tender weeks of migration; captive rearing in vast numbers, though done with reverence, may carry unintended risks of disease and weakened orientation. The monarch asks us to enlarge our sense of home beyond the fence: to let patches of milkweed lift their pale crowns in rough corners; to choose late-blooming asters and goldenrod; to keep a few ditches shaggy until the travelers pass. Conservation, like metamorphosis, is work that happens inside ordinary days.

Watch the cycle again in my images—egg to appetite, appetite to stillness, stillness to wing—and hear what it whispers in the steady voice of milkweed leaves and soft fall air. Rachel Carson wrote that “those who contemplate the beauty of the earth find reserves of strength that will endure as long as life lasts.” Here beauty wears stripes and beads of gold, sips from garden petals, and threads a continent with its frail insistence. The monarch’s life is a ribbon we can follow with our eyes and, if we are willing, with our hands—gentle hands that leave room for milkweed to rise, for caterpillars to feed, for a chrysalis to darken and a window to fill, one bright morning, with wings.

On a personal note, this season was a success. Monarchs visited our milkweed patch several times allowing me to save/harvest nineteen eggs/caterpillars and raise them until release.

Selected references
Carson, Rachel. The Sense of Wonder. New York: Harper & Row, 1965. (Reissued: HarperCollins, 1998; Open Road Media e-book, 2011.) The quoted passage (“Those who contemplate the beauty of the earth…”) appears early in the book; the Open Road edition places it on p. 41.
Wikipedia contributors. “Monarch butterfly — Etymology and taxonomy.” (useful overview with primary citations).
Oberhauser, K. S., and M. J. Solensky, eds. The Monarch Butterfly: Biology and Conservation. Cornell University Press, 2004.

Enter your email to receive notification of future postings. I will not sell or share your email address.

Buttonbush: The Secret Geometry of Wetlands

Discover the Buttonbush (Cephalanthus occidentalis), a wetland shrub of spherical blooms, sustaining pollinators, birds, and waterfowl while reminding us of life’s enduring cycles

MichaelStephenWills9 Comments

In the quiet wetlands of late summer, when cattails lift their brown torches above the reeds and dragonflies skim the still water, there is a shrub that speaks in spheres. Its language is not the pointed spear of grass or the broad fan of lily pads, but the perfect symmetry of globes—round, intricate, and startling in their precision. This is the Buttonbush, Cephalanthus occidentalis, a native of swamps, pond margins, and the soft, yielding soils where water shapes the land.

At first glance, its clusters might be mistaken for something fashioned by human hands: spiky balls arrayed along slender stems, each one a small planet bristling with tiny cells. Only in memory can we recall their summer incarnation, when each ball was a constellation of snowy blossoms, white tubular flowers extending like delicate pins from a spherical center. Bees and butterflies crowded them then, drunk on nectar, wings glinting in the sun. Hummingbirds darted in as though drawn by an unseen magnet, their beaks fitting perfectly into the narrow blossoms, a partnership written long ago in the shared script of evolution.

Buttonbush (Cephalanthus occidentalis) at Sapsucker Woods, Cornell Lab of Ornithology

Now, in August’s waning light, those blossoms have folded back into seed, transforming into the russet orbs captured in the photograph. What was once nectar is now promise—food for ducks, shorebirds, and the small lives that depend on wetlands for sustenance. In the hands of buttonbush, time itself is circular. Flower becomes fruit, fruit becomes seed, seed becomes shrub, and the cycle spins quietly on, just as the spheres themselves suggest: complete, unbroken, eternal.

A Wetland Companion

Buttonbush is rarely alone. It thrives where cattails whisper, where pickerelweed thrusts up spikes of purple bloom, where the air holds the scent of waterlogged earth. Its roots grip the muck at the edges of ponds and rivers, holding soil against the restless tug of currents. In doing so, it becomes part of the unseen architecture that holds wetlands together, slowing erosion, filtering water, providing shelter for fish in the shade of its stems.

Pickerelweed (Pontederia cordata) at Sapsucker Woods, Cornell Lab of Ornithology

This shrub, unassuming in stature, is an engineer of stability. It creates thickets where red-winged blackbirds perch, where frogs crouch in shade, where turtles bask on half-submerged branches. The wetlands of North America would be poorer without its presence, for it provides not just beauty but the scaffolding upon which entire communities of life depend.

The Human Thread

To the human eye, the buttonbush’s spherical blooms are so striking that they demand metaphor. Some have called them pincushions, others tiny planets, others fireworks arrested in mid-burst. Native American peoples, however, looked beyond metaphor to medicine. The bark and roots were used in remedies for ailments ranging from headaches to fevers, though with caution, for the plant holds mild toxicity when consumed raw. It is a reminder that many gifts of the natural world are edged with danger, and that wisdom lies in balance.

Today, gardeners and conservationists plant buttonbush intentionally. It is welcomed into rain gardens, where its thirst for moisture makes it a perfect ally for absorbing stormwater. It is used in wetland restoration projects, where its deep roots anchor new life. And it is cherished by those who walk the edges of ponds and discover in its round blossoms a geometry that feels both wild and deliberate, a gift of design from the living earth.

Fourth of July, 2019, Stewart Park

The Sphere as Symbol

Rachel Carson once wrote that in nature, “nothing exists alone.” The buttonbush embodies this truth with clarity. Its spheres are invitations, junctions where plant and pollinator meet, where flower and bird share a moment of mutual necessity. They are offerings to the eye as well, challenging us to see patterns where we might otherwise see only happenstance.

Standing before a buttonbush in bloom, one feels an almost childlike wonder: how could such symmetry arise unbidden from soil and sunlight? Yet this is the miracle of evolution, that order may spring from chance, that beauty may serve survival, that what pleases our senses also sustains life.

A Closing Reflection

In the wetlands, where water mirrors the sky, the buttonbush offers its own reflection of completeness. Its seed heads persist through autumn and winter, small orbs clinging even when leaves fall, reminders that the cycles of life turn steadily beneath the stillness.

To linger with buttonbush is to be reminded of nature’s quiet insistence on wholeness. It speaks in forms: round, repeating, enduring. To walk away from it is to carry a sense of connection, to know that in the pattern of its blooms we glimpse a truth both humble and profound—that life is not a line but a circle, and in every turning there is renewal.

For Further Reading

USDA NRCS. Plant Guide: Buttonbush (Cephalanthus occidentalis L.). United States Department of Agriculture, Natural Resources Conservation Service. Available online: https://plants.usda.gov
– Provides detailed information on identification, habitat, and ecological role.

Lady Bird Johnson Wildflower Center. Cephalanthus occidentalis (Common Buttonbush). Native Plant Information Network. Available online: https://www.wildflower.org/plants/result.php?id_plant=ceoc2
– Covers botanical features, bloom time, wildlife value, and landscape use.

Dirr, Michael A. Manual of Woody Landscape Plants: Their Identification, Ornamental Characteristics, Culture, Propagation and Uses. 6th Edition. Stipes Publishing, 2009.
– Authoritative horticultural reference on Buttonbush and other shrubs.

Peterson, Roger Tory, and Margaret McKenny. A Field Guide to Wildflowers: Northeastern and North-central North America. Houghton Mifflin, 1968.
– Classic field guide covering buttonbush’s wetland habitat.

Carson, Rachel. Silent Spring. Houghton Mifflin, 1962.
– Source of the quoted passage: “In nature nothing exists alone.” (Chapter 2, “The Obligation to Endure”).

Moerman, Daniel E. Native American Ethnobotany. Timber Press, 1998.
– Comprehensive reference documenting traditional medicinal uses of Buttonbush among Native American peoples.

Enter your email to receive notification of future postings. I will not sell or share your email address.

The Secret Life of Woodland Plants: Jack-in-the-Pulpit Insights

In the hush of the forest, Jack-in-the-Pulpit speaks—not with sound, but with form and patience, reminding us that some sermons rise quietly from the earth.

MichaelStephenWills19 Comments

You could walk past it a hundred times and never notice. There, beneath the low canopy of midsummer, where light is sifted through green, Arisaema triphyllum stands with the discretion of a shadow. Jack-in-the-Pulpit, they call it—a name as strange and gentle as the plant itself. But neither common name nor scientific binomial quite captures the feeling that you are being addressed when you encounter one.

A young Jack-in-the-pulpit under its leaf canopy along the gorge trail of Filmore Glen.

A mature Jack-in-the=pulpit flower with purple trillium, Fillmore Glen.

Earlier in the year, it raised a hooded spathe above the forest floor, curving protectively over a pale central spadix—the “Jack.” It looked like a figure delivering a sermon to the moss and littered leaves. Now, that sermon has passed, and the speaker has fallen silent. What remains is a column of tight green berries, glinting softly in the dappled light. They are not yet ripe, but the promise is there. In time, they will glow red like embers in the undergrowth.

Summertime, Sapsucker Woods. I might use a colloquialism and call this plant a “Jill”….and the real twist? Jack might’ve started out giving sermons but give them a good season and a strong root system, and Jack becomes Jill. It’s sequential hermaphroditism at its finest—Mother Nature’s version of career flexibility.

There is something ancient about this plant, as if it remembers a forest before our footsteps came. Its roots delve deep, not just into the soil, but into time. A corm, nestled beneath the leaf mold, waits out the harsh seasons, unseen but enduring. It is not a showy plant. It is a plant that trusts quiet. That survives on patience.

A closer look at the unripe berries.

The forest is full of these secret lives—beings that do not shout to be known. Jack-in-the-Pulpit speaks softly, in a dialect of leaf and shade and seasonal return. It is a plant you find when you have slowed down enough to belong again to the forest’s rhythm, when you’ve traded the voice in your head for the breath of leaf litter underfoot.

From Fillmore Glen

Some would call it just another spring ephemeral, a curiosity among many. But to walk away from it without feeling a kind of reverence would be to miss the point. It is not there to impress. It is there to remind.

That not all things are revealed at once.
That sermons come in many forms.
And that in the hush of the forest, something is always speaking—if only we remember how to listen.

Enter your email to receive notification of future postings. I will not sell or share your email address.

Discover the Bold Jumping Spider: Nature’s Agile Hunter

Small in size but vast in charisma, the Bold Jumping Spider hunts with precision, agility, and a gaze that almost seems to return your own.

MichaelStephenWills11 Comments


There, pressed into the grain of the boardwalk like a dark fleck of forest lint, the Bold Jumping Spider (Phidippus audax) waits—motionless, yet alert. To the untrained eye, it may seem insignificant, even nondescript. But a closer look reveals a creature of fine design and surprising charisma: a compact body cloaked in velvety black, adorned with pale markings like runes, and forward-facing eyes that gleam with eerie intelligence.

Unlike the orb weavers and net-spinners of spider lore, Phidippus audax does not rely on traps. It is a hunter in the truest sense—an animal that lives by leaping toward its future. With eight powerful legs and a muscular abdomen, it can launch itself many times its own body length, arcing through the air toward an unsuspecting moth or beetle. Yet it does not leap blindly. It trails a single silken thread behind it—a safety line, a commitment to survival. It is an act of courage tethered to caution.

Most remarkable are its eyes. A quartet of simple lateral eyes scan for motion, but the two large, front-facing principal eyes are something more—a rarity among arthropods. They grant it acute vision, with the ability to detect detail, movement, and even depth. When it turns its gaze toward you, you feel seen—not just registered, but regarded.

Found lurking in a joint of wood frame enclosing a trail map. Sapsucker Woods, Cornell Lab of Ornithology, on a summer afternoon\.

These spiders are active thinkers, decision-makers. They test their environment with movements that can almost be described as exploratory. They do not walk so much as prowl, stepping into shadow and light with an awareness that seems out of scale for their size.

And though they are often met with fear or disdain, Phidippus audax poses no threat to humans. It asks only for a few square inches of wood or leaf to stake its claim. In return, it offers a glimpse into a different kind of grace—an agile, silk-spinning daredevil, leaping with acute precision.

To observe one is to witness the meeting of design and instinct, form and function, in perfect miniature. In the vast, humming network of woodland life, the Bold Jumping Spider may be a small player, but it performs its role with flair. If the trees are the spires of the forest cathedral, and the ferns its leafy congregation, then Phidippus audax is a kind of sacred rogue—silent, swift, and utterly unconcerned by our towering presence.

Enter your email to receive notification of future postings. I will not sell or share your email address.