Wooster Memorial Park Field Trip – Hydrology Lab Fall – 2026

Guest bloggers: Amrin Sazia, Amelia Crowley, Keiryn Keener and Maddie Ostapchenko.

Figure 1. Our Hydrology class during the field trip at Wooster Memorial Park (Buried valley).

On the 7th September 2026, our Hydrology class visited Wooster Memorial Park to look at how geology and water work together to shape the landscape around Wooster. During the trip, we stopped at six places to see how glaciers and erosion shaped the landscape and bedrock around Wooster. The main goal was to see some of the features we had discussed in class and understand how they affect the movement of water. The weather was pretty sunny on that day, and we got to eat apples for hydration.

Figure 2: Dr. Wiles pointed out how this rock that was not native, it was a glacial erratic which came here most probably 20,000 years ago during the last ice age. The clast is a bullet shaped boulder, a tillite from Snowball Earth time hundreds of millions of years ago. A sedimentologist would classify it as a matrix-supported diamictite.

Figure 3:  At Site 3, we looked at alluvial fans. These are areas where sediment carried by small streams builds up at the bottom of a slope. They were hard to see from the ground because of all the trees, but they were much easier to recognize on the LiDAR map. Dr. Wiles also explained that the sediment in these fans is very permeable, so water can soak into the ground and recharge groundwater .

Figure 4: At Site 4, we talked about how people have changed the landscape over time. The area used to have mills and mill ponds, and fine sediment collected behind the dams. Some of this old sediment is still being eroded into the stream today. We also saw how much the stream has changed and cut down through the landscape over time.

Figure 5: At Site 5, we saw a large exposure of sediment that helped us understand the buried valley. The valley was filled with sediment during and after glaciation, and some of the material was also moved by meltwater streams. These sand and gravel deposits are important because they can store groundwater and form aquifers.

 

Figure 6: At our last stop, we looked at compact glacial till along the stream bank. The till is packed very tightly, so water cannot move through it easily. Instead, groundwater moves along the top of the till and comes out as a spring. Gabe tried to find the wet layer using a well point, and we could see orange iron staining where the groundwater was coming from.

 

Overall, the field trip helped us see how Wooster Memorial Park has changed over time. We talked about how it changed after the Last Glacial Maximum till now. It was interesting to see the same features we talked about in class out in the field. Some parts of the park also look very different from photos taken only a few years ago because the stream is still actively eroding the landscape.

 

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Hydrology 26 Springs into Action!

Guest Bloggers: Eddie Fatica, Nolan Hendricks, Stephen Shickluna, Gabe Jones, Sihan Tian

Figure 1. The hydrology team at Geyers Chapel spring.

Background:

This week, our hydrology class explored the physics and functionality of natural springs in our wonderful Wooster, Ohio. We visited three locations during this lab, including Kinney Fields, Geyer’s Chapel, and the beautiful Secrest Arboretum, to observe and test springs firsthand. At each site, we examined how factors like geology, surrounding agriculture, water table depth, and aquifer pressure influence the way a spring forms and flows. We also took measurements of water quality and water temperature to help us compare each of the 3 springs to each other.

Methods:

At each area we visited, we performed a series of tasks to help compare each spring. We checked the water temperature of each spring to determine how deep the water had traveled underground. The colder the water, the deeper it had traveled from underground. Then, our T.A., Arjan collected water samples from each spring, which will be used in the future to tell us the components of each spring. Lastly, we used the probe to help determine how far the spring was from the bedrock, as well as what kind of material was around and under the stream (Figure 2.).

Figure 2. Eddie F. using the tile probe to locate bedrock.

Figure 3.  T.A. Arjan taking the temperature of the spring water.

Figure 4.  Arjan taking a water sample at Secrest Arboretum.

Results:

At our first site, the Mckinney fields (40°49’50.81″N, 81°56’28.62″W), we were able to identify colluvial deposits near the site of the well house . We identified the overburden as glacial till/clay and assumed the water table was under that. (Figure 5.) Measurements revealed the water temperature to be 13.9 C, showing that this area was, indeed, a spring. It should be noted that while we did take samples to determine the water chemistry at each site, those results have not been revealed to us yet. After taking the water temperature at the first site we moved to Geyer’s Chapel (40°52’42.31″N, 81°53’50.75″W) finding the water temperature to be at 12.6C, warmer than the last site, yet still indicative of a spring. Our third and final site was Seacrest abortorium (40°47’0.50″N, 81°55’19.65″W).  This spring, being a seep spring, had a temperature of 15.2C. Here we were able to identify an unconformity after poking around with a tile probe. We found very hard rock about 2-3 feet under the water. This rock was assumed to be a few hundred million years old while the glacial clay that overlayed it was assumed to be 20,000 years old.

Figure 5. A sketch of the well-house and the surrounding geology.

Closing Thoughts:

This fieldtrip was a great practicum in determining where springs may be located, what kind of rock may be surrounding them, and how to use certain tools to assist in these processes. When field tests and models such as the 3-point problem are combined, determining stream flow becomes easy. Knowing the direction a stream flows is essential for contaminants / pollution management and prevention for municipalities.

The class at the CFAES weather station that provides hydrologic information back to the mid 19th century.

ODNR Monitoring Well on the grounds of the CFAES campus.

 

 

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Hydrology (HYDRO26) Lab Macroinvertebrate Survey

Guest bloggers: Anika Knowles, Cheyenne Wentz, Ellie White and Leo Casalini

The HYDRO ’26 Macroinvertebrate team.

The Objective

The team gathered before starting the survey at Site 1.

Students enrolled in this year’s Hydrology course took a trip down to Apple Creek, a local tributary of the larger Killbuck Creek, to aid in the completion of a macroinvertebrate survey led by entomologist Carrie Elvey of Ohio State University and Steve of Trout Unlimited. The survey was done with the express goal of assessing the current health of Apple Creek and by extension to add to the larger understanding of its health over the years. By surveying the amount and the type of critters, or macroinvertebrates, found in the stream, an estimation could be made of the creek’s health. A healthy stream is a diverse and plentiful one.

Methods & Collection

Three of the HYDRO ’26 team (Amrin, Gabe, and Amelia from left to right) using the Kick Siene net.

Survey sites 1 and 2 (labeled in yellow) along Apple Creek.

The macroinvertebrate survey was done by splitting up and using different methods of collection. Both Dip nets and Kick Siene nets were used to catch the macroinvertebrates, as well as the basic method of picking up a rock and seeing if any macroinvertebrates were on it. This was done for about 20 minutes. Macroinvertebrates were placed into two bins for safe keeping until being separated further into a smaller tray based on species. The different types of species were then recorded. The same process was then repeated at site 2.

Macroinvertebrates separated by species in an ice cube tray.

Carrie Elvey helped the class learn how to identify the macroinvertebrates that were found and how to distinguish between similarly shaped ones. For example, in the top left corner of the ice cube tray above, there are two critters that may seem the same. Upon closer inspection, one of them has visible gills along its abdomen, a characteristic of a mayfly. The other critter without visible gills on its abdomen is a stonefly, as their gill tufts are under their arms.

Figure 1. Apple Creek’s reported annual stream health from 2012 to 2026 as recorded from site #1.

Figure 2. Apple Creek’s reported annual stream health from 2012 to 2026 as recorded from site #2.

Results

Based on our surveys, both of the sites have excellent water quality. Site 1 scored 27 (Figure 1) and Site 2 scored 37 (Figure 2), both above the threshold of 23. In Site 2, we found more of the species sensitive to changes in water conditions and chemistry, including a right-handed snail, dobsonfly larvae, and sow bug, hence the higher score. Both sites had caddis fly, mayfly, stonefly, blood midge, water pennies, left-handed snails, among other invertebrates. While these numbers indicate that the water quality is excellent, the scores have declined since the survey process began in 2012. This could potentially be due to the nearby cement plant, recent storm/flood events, or the history of dredging and oil spills, that could have increased runoff into Apple Creek.

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Master Dating of a Master’s Panel Painting

A first for the Wooster Tree Ring Lab (WTRL) – dating a 17th century painting from the Rembrandt Studio in the Netherlands.

Nick Wiesenberg, technician in the lab (right) and the owner of the painting James Elchlinger from Zora Advisory Group. The painting is titled “A Scholar in His Study” possibly painted by Gerbrand van den Eeckhout of Rembrandt Van Rijn’s studio. This panel painting was on an oak panel that had over 240 rings. The mission was to measure the ring widths and then to use dendrochronology to assign calendar dates to each ring by comparing (aka crossdating) ring-width measurements to a master chronology that is calendar-dated. A tree-ring date would help validate the authenticity of the painting.

A close-up of the painting.

The first step was to prepare the surface of the oak panel by carefully sanding the top of the painting to be sure that the wood cells within each ring were visible. Dr. Hernán Medina (standing; Wooster Spanish Professor) and Anika Knowles (lower right; Wooster Earth Science/Spanish major and Alaska Tree Ring worker) look on.

The oak panel is made of three panels glued together, and is only about 5 mm thick; the back of the painting is bolstered by a “cradle” of oak laths. This detail shows the ring porous structure of the individual oak rings (rings are horizontal) the vertical lines in the wood are rays of the oak tree. Toward the top of the image is a portion of the oak cradle.

Nick scanned the prepared (sanded) top edge of the panel (note the painting is upside down). From the image on the computer screen he was then able measure the ring widths from the image. The images and measurements were then sent to a lab in Hamburg Germany that specializes in dating artwork and other materials from Northern Europe using tree-rings.

A closeup of the scanned image showing the oak rings.

 

As Gerbrand van den Eeckhout was an understudy in the Rembrandt Van Rijn studio of the Netherlands, Adam Wood is an understudy in the Wooster Tree Ring Lab in Northeast Ohio. 

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Wooster student learns to live small at Diatom Camp

Guest blogger: Anna Lundquist (ESCI and PHIL double-major, class of 2027)

Diatoms are microscopic, single-cellular algae that build their skeletons (called frustules) out of silica, aka glass! They are extremely abundant, living basically anywhere they can find water and sunlight, in both freshwater and marine environments; in fact, they produce over half of the Earth’s oxygen. They are also very sensitive to environmental change, and preserve well, making them excellent for all kinds of paleoecological analysis.

This summer I attended the 63rd annual 2026 Iowa Lakeside Lab Ecology of Systematics of Diatoms course, lovingly nicknamed Diatom Camp, a month-long summer class that gave me the opportunity to spend a month at the University of Iowa’s field station in Okoboji, Iowa.

MacBride Lab, where we spent our class (and microscope!) time

There, I spent time learning about diatom taxonomy and how they can be used for paleolimnological interpretation, as well as spending lots of time in the field. The campus is located right next to a lake on 147 acres of prairie. Through the course, I got to explore prairie, fen, lake, river, and bog environments, under the microscope and in the field! The most important material I will be working with for my Senior Independent Study are lake core samples, so getting the opportunity to take and work with fresh lake cores and surface samples in a field setting in Iowa was an especially exciting experience.

Collecting a sediment sample from West Lake Okoboji using the Ponar surface sampler

Exploring Silver Lake Fen, a calcareous wetland filled with unique muck and marl pools

Over the course of the class, we got to work with samples not just from Iowa, but also marine estuaries in Florida, and streams from Minesota’s North Shore, which is currently facing an infestation of invasive didymo, or rock snot, the only diatom with a common name. Rock snot forms slimy brown mats of mucilage, a mucus-like substance that diatoms secrete to help them anchor to a substrate, on the bottom of otherwise clean and low nutrient streams. This is a nuisance to both human and non-human visitors to the streams, with didymo choking out everything else living in the streams. In class, we looked at samples from North Shore streams, to help assess the spread of didymo, as well as looking at the other kinds of diatoms present.

A living sample of didymo, showing the mucilage stalk. Photo courtesy of Sarah Spaulding via diatoms.org.

As the only undergraduate student in the class, I also was able to meet graduate students working on a diverse range of projects in geology, paleontology, and environmental science. Over the course of the class, I got to learn about their research as well as getting to work alongside them as peers and friends.

Our class photo in front of MacBride Lab

I was taking this course to support my Independent Study, which will investigate the effects of climate change and human activity on two small lakes in the eastern Sierra Nevada using diatom stratigraphy. Over the next year, I hope to use my newly gained diatom knowledge to track and compare palaeoecological changes in these two lakes using core samples. I also hope to examine surface sediment samples to map out a biogeographical profile of the sediment characteristics and diatom communities living in different areas of both lakes.

Looking in the microscope

The view through the scope!

My experience in this course would not have been possible without the support of Wooster’s Copeland fund and Earth Science department’s Davis fund, and I am so grateful to have had this opportunity!

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New paper on Ordovician cryptic marine ecosystems

My Estonian friend and colleague Olev Vinn led a team reviewing the ecological innovation of organisms encrusting the interiors of mollusk shells in the Ordovician. It is yet another example of the extraordinary diversification of marine organisms in this period. The image above is a reconstruction of bryozoans and cornulitids in an empty snail shell on an Ordovician seafloor. Our paper is just out as early access in Scientific Reports (Vinn et al., 2026).

Abstract:

In all modern seas, empty mollusc shell interiors are often heavily encrusted by cryptic invertebrates, whereas globally in the Cambrian, all shell interiors of molluscs and other invertebrates remained free of encrustation, though cryptic organisms themselves occurred in other types of cavities. The colonization of cryptic surfaces within empty shells constitutes a global event and an important ecological innovation in Ordovician benthic marine ecosystems, marking the beginning of a new ecological niche. The earliest colonization in mollusc shells by cryptic invertebrates occurred in the Middle Ordovician, while heavily encrusted shell interiors are known since the Late Ordovician. The taxonomic composition of Ordovician cryptic communities in gastropod, bivalve, and nautiloid shells is generally similar, though substrate architecture influenced encruster abundance and body size rather than overall community structure. The major expansion of cryptic ecological niches occurred during the Ordovician biodiversification, driven by the increase in predation pressure, the diversification of encrusting organisms, and a general increase in the size of mollusc shells.

Reference:

Vinn, O., Wilson, M.A., Tinn, O., Lang, L., Isakar, M. and Toom, U. 2026. Colonization of empty shells by cryptic fauna: a global event and important ecological innovation in Ordovician benthic ecosystems. Scientific Reports (early access); https://doi.org/10.1038/s41598-026-62638-5.

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The 2025-2026 Earth Sciences Annual Report is Out

Great to see that The College of Wooster Earth Sciences Annual Report is now out. Thanks to Nat McCoy (ESCI Administrative Coordinator) and Dr. Meagen Pollock (ESCI Chair) for their hard work in assembling this record of all the activities over the past year. You can access a copy here.

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Wooster Geologists Ketchikan Blog

A couple of dudes on Dude Mountain

Guest bloggers – Cheyenne Wentz and Anika Knowles: Day 1 (June 23rd): We arrived in Ketchikan and took the ferry across the fjord from the airport to Revillagigedo Island (where the town of Ketchikan is located). After picking up our rental car, we drove to Rotary Beach and explored the tide pools for a few hours. We saw lots of life, including mussels, sea snails, kelp, crabs, and 51 sea stars. We also were introduced to salmon berries, and we picked and ate an abundance of the red-orange fruit. After a dinner of pasta, we caught the end of sunset over the water.

Ferry ride from the airport to Ketchikan. 

Pointing out sea stars at Rotary Beach tide pools. 

Ochre Sea Star (left) and salmon berries (right)

Day 2 (June 24th): For our first day in the field, we went to Perseverance Lake and hiked around, learning the difference between red cedar and yellow cedar while marveling at all the other flora and fauna including banana slugs, sundew, alder trees, and many different ferns. We also learned to identify devil’s club and cow parsnip, both plants that you don’t want to touch. We had lunch on some logs overlooking the lake, then began coring trees and preserving them in straws.

Red cedar – less dense foliage, sweeter smelling, flatter needles

Yellow cedar – more dense foliage, kind of citrus smelling, rounder needles, more droopy

Yellow cedar (left) and redcedar (right)

Cheyenne and Nick extracting a redcedar core.

Perseverance Lake.

Day 3 (June 25th): In the morning, we had some local coffee along with our breakfast before heading back to the Perseverance trail to continue coring redcedar and complete that site’s chronology. It was raining almost the whole day, so we sported our fashionable yellow raincoats. We saw LOTS of skunk cabbage and devil’s club, along with a few more banana slugs, on our way to the trees. For coring, we tried to choose trees that weren’t leaning at a big angle, didn’t have visible rot, and were decently large. We noticed that the redcedar is much easier to core than the yellow cedar, which our triceps thanked us for. We had lunch on a mossy knoll and then traversed to a lake with no name where we saw some trees that had been stripped, a traditional practice of the Tlingit and Haida indigenous peoples. After the day’s work, we stopped at Connell Dam and Totem Bight State Park where we learned a little bit more about the Tlingit and Haida culture and history. We finished the day with taco Thursday complete with bean juice and cinnamon tortillas (shoutout WOODs club!).

Cheyenne and Anika standing by a stripped redcedar.

Anika and Cheyenne coring a redcedar.

Connell Dam (left) and Totem Bight State Park (right).

Day 4 (June 26th): We continued on to our second site—Lunch Creek Trail. We explored the trail to scope out where the best redcedars were to core, then stopped for lunch at a bear-frequented spot where we set up a hammock. As we cored trees, we found some ripe wild blueberries and talked to some friendly hikers. After the day’s work, we hiked down to Settler’s Cove to sit and watch the water for a bit.

Settler’s Cove

Day 5: After three days of hard work, we had a chance to explore around Ketchikan and rest a little. We spent a few hours at the Southeast Alaska Discovery Center where we learned some more about the natural history of the area. Fun fact, Tongass National Forest is the largest national forest in the country! We also heard from one of the retired loggers and his experience in the timber and wood pulp industry.

Yellow cedar drawing (left) and Anika taking notes (right).

Day 6: We drove to Dude Mountain Trail and hiked to the summit which was very foggy but we got some good views as the clouds moved. We had lunch up at the summit then cored mountain hemlocks and yellow cedars on the way down, trying not to eat any of the bugs that were swarming us. There was a sweet spot in the middle where the most reliable trees to core were. We also learned the difference between mountain hemlock and western hemlock. Hemlocks are a hard wood, compared to the cedars which are a soft wood, so it was a lot harder to core the hemlocks. We also found some core holes from the previous Wooster trip to Ketchikan (shoutout Amanda and Proto).

Mountain hemlock – needles all the way around the branch

Western hemlock – needles two-dimensional/parallel

Cheyenne and Anika coring a Mountain Hemlock.

Fog on Dude Mountain.

One more day of sampling and then a trip to Misty Fiords before returning to Wooster for data processing.

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The Phylum Bryozoa is now known from the Cambrian. An updated set of posts.

The vexing question of the earliest bryozoans has now been definitively answered. The Phylum Bryozoa appears first in early Cambrian rocks in China (Song et al., 2026). Until recently they were one of the few major animal phyla not represented in the Cambrian. Because I had a minor role in the story, I’ve twice updated a 2012 blog post of mine and made this composite entry to give a sense of the history of the Cambrian bryozoan issue. I start with the recent news and work back to 2012.

Editor’s Second Note: Yesterday (June 3, 2026) an article appeared in Nature by Song et al. (2026) with the decisive title: “High-fidelity modular skeletons authenticate a Cambrian origin for Bryozoa.” Here is its abstract:

The major animal body plans originated during the Cambrian explosion, yet the
phylum Bryozoa has remained a conspicuous exception to this pattern. The initial
discovery of Protomelission gatehousei provided compelling evidence for a Cambrian
origin for the Bryozoa, together with other major metazoan phyla and compatible
with independent molecular clock estimates. Nevertheless, the scarcity of definitive
soft-tissue anatomy and diagnostic skeletal microstructure has left its phylogenetic
affinities ambiguous and debated. Here we report exquisite fossils of P. gatehousei
and a new taxon, Dayingomelission hexaclitia gen. et sp. nov., from the early Cambrian
Xiannüdong Formation of China. These specimens preserve in situ phosphatized
soft tissues in modular skeletons, revealing critical anatomical structures, including
styles, annular muscles, membranous sacs and ring septa. This suite of traits provides
definitive evidence that these taxa belong to the Bryozoa. Phylogenetic analysis
incorporating these new features identifies them as crown group stenolaemates.
These results confirm a Cambrian origin for the phylum and reveal an unexpected
early disparity in colonial architecture, demonstrating that bryozoan diversification
was an integral component of the Cambrian radiation. Moreover, the early appearance
of a differentiated stenolaemate crown group indicates a still deeper origin for the
bryozoan stem lineage than was first apparent.

The top images are from Figure 1 (a-f) of Song et al. (2026): Specimen of Protomelission gatehousei from the Xiannüdong Formation in which the membranous sacs are preserved. Scale bars: 500 μm (a–d), 50 μm (e), 200 μm (f).

Image above from an Uppsala University press release: “The newly discovered bryozoans were only a few millimetres in size and lived attached to the seabed in shallow tropical seas. The image is a reconstruction of what they may have looked like. Illustration: Zhifei Zhang.”

We can now conclude that Protomelission gatehousei and Dayingomelission hexaclitia are Cambrian bryozoans, and Pywackia is not. The Phylum Bryozoa is known in the fossil record from the early Cambrian. Time to update textbooks and databases!

Editor’s First Note: The post below was written in December 2012 about a purported bryozoan found in Cambrian rocks. This would have been a major find because bryozoans, a major fossilized phylum, were notably missing from the Cambrian record, despite molecular evidence that they must have been there. The fossil described in this old post is almost certainly not a bryozoan, but NOW a recent publication describes clear and distinct bryozoans from the Early Cambrian of Australia and South China: Zhang, Z., Zhang, Z., Ma, J., Taylor. P.D., Strotz, L.C., Jacquet, S.M., Skovsted, C.B., Chen, F., Han, J. & Brock, G.A. 2021. Fossil evidence unveils an early Cambrian origin for Bryozoa. Nature; https://doi.org/10.1038/s41586-021-04033-w. (Note that friend of the department Paul Taylor is among the authors.) The new bryozoan fossil is erect, bilaminate, and secondarily phosphatized. Its taxonomic name is Protomelission gatehousei. Andrej Ernst and I wrote a Nature News & Views article about this fantastic story. Now we all must update our lectures on bryozoans and the Cambrian radiation!

The original December 2012 post (now more than 14 years old!) is below.

_______________________________________________

Screen shot 2012-12-17 at 6.01.54 PMDUBLIN, IRELAND — It was a great day of talks at the 56th Palaeontological Association Annual Meeting being held at University College Dublin. I learned many things, from new ideas about the Burgess Shale and its characteristic fauna to why there is no demonstrated sexual dimorphism among Mesozoic vertebrates. (I also learned that the students in this university must sit in very cramped spaces in chilly rooms. Wooster students: note your classroom comforts!) My favorite talk of the day was one on which I was a co-author: “Is the world’s oldest bryozoan actually the world’s oldest pennatulacean?” Our senior author and genius of the project, Paul Taylor, gave the lecture. I’m presenting here two slides from the PowerPoint presentation. We’ll have much more about this topic when we have our paper on it in press. In the top image you see on the left Pywackia baileyi, a putative Cambrian bryozoan recently described in a high-profile journal. This is a big deal because bryozoans are known as one of the very few phyla not found in the Cambrian. We looked at the evidence and the specimens and quickly concluded this Pywackia baileyi is not a bryozoan. (Tell your friends!). Instead it appears to be pennatulacean-like octocoral. The image in the top right is of Lituaria, a modern pennatulacean. Note how similar these structures are, except for almost an order of magnitude size difference (which is reduced when looking at the range of sizes in other pennatulaceans).

Screen shot 2012-12-17 at 6.03.34 PMIn the above slide from Paul’s presentation you see Pywackia and Lituaria again on the left, and then a variety of living pennatulacean octocorals on the right. We have strong evidence, from the morphology to the possible original phosphatic composition, that Pywackia baileyi is not the earliest bryozoan. We have thus far a good case that it instead represents the earliest pennatulacean octocoral. Again, this story will be developed further later in this blog after our paper is accepted for publication.

Jameson121712The day ended with the traditional, raucous annual Palaeontological Association dinner at the Jameson Distillery in downtown Dublin. In the above image you can see in the foreground on the right Wooster alumna Lisa Park Boush and her husband Carlton. We are among just a scattering of Americans at this European meeting. It was a very pleasant (if very loud) evening!

References:

Landing, E., English, A. and Keppie, J.D. 2010. Cambrian origin of all skeletalized metazoan phyla—Discovery of Earth’s oldest bryozoans (Upper Cambrian, southern Mexico). Geology 38: 547-550.

Song, B., Zhifei Z., Strotz, L.C., Topper, T.P., Ernst, A., Ma, J., Zhang, Z., Luo, M., and Holmer, L.E. 2026. High-fidelity modular skeletons authenticate a Cambrian origin for Bryozoa. Nature; https://doi.org/10.1038/s41586-026-10590-9

Taylor, P.D., Berning, B. and Wilson, M.A. 2012. Is the world’s oldest bryozoan actually the world’s oldest pennatulacean? Palaeontological Association 56th Annual Meeting, Dublin, Ireland, Programme and Abstracts, p. 52.

Zhang, Z., Ma, J., Taylor. P.D., Strotz, L.C., Jacquet, S.M., Skovsted, C.B., Chen, F., Han, J. & Brock, G.A. 2021. Fossil evidence unveils an early Cambrian origin for Bryozoa. Nature; https://doi.org/10.1038/s41586-021-04033-w.

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Wooster’s connection to the world’s deepest bryozoans

Earlier this month a remarkable paper appeared in the journal Science entitled: “Protist-­dominated hard substrate faunas thrive at the deepest ocean depths”. If you know any of my scientific enthusiasms, you know I very much love hard substrate faunas through space and time. The article by Song et al. (2026) describes a community of organisms found by the submersible Fendouzhe at extreme hadal depths (9,000 to 10,898 meters) in the Kermadec and Mariana trenches. Among the 32 species is a little soft-bodied bryozoan given the name Pierrella fendouzhei. Again, among my scientific passions is the study of bryozoans. This particular species now has the depth record for the Phylum Bryozoa: 9981 meters, about 6.2 miles down. For context, the wreck of the Titanic is 3800 meters deep, so Pierrella fendouzhei is living on rocky surfaces up to 2.5 times deeper than the legendary ship. The top image is from Figure 1F of Song et al. (2026). It shows Pierrella fendouzhei as series of connected white ovals. The scale bar is 3 cm.

Now the Wooster connection. The genus Pierrella was first described and named by me and Paul Taylor in 2012 for a group of delicate fossils inside ammonite conchs collected from the Upper Cretaceous (Campanian-Maastrichtian) of the Pierre Shale in South Dakota and Wyoming (Wilson and Taylor, 2012; see figure above; scale bars are 10 and 5 mm respectively). The fossils show a spindly series of connected tear-drop shapes that were entombed by exquisite mineralization. The original bryozoans were entirely soft-bodied, so this is a rare form of preservation. We collected these fossils on an Independent Study field trip in 2008 with Wooster student John Sime.

So the first described Pierrella bryozoan was a 70-million-year-old fossil from the Cretaceous Western Interior Seaway of North America. It probably lived in these shell interiors at the muddy bottom of these roughly 700 meters down. Above is an image of an ammonite internal mold with chains of Pierrella zooids.

In 2018, a Russian-led scientific team collected metalliferous seafloor nodules in the Clarion-Clipperton Fracture Zone of the eastern Pacific at roughly 5000 meter depths (Grischenko et al., 2018). Astonishingly, they found living examples of our bryozoan Pierrella. This genus now had an unusual two-point distribution: a Cretaceous inland seaway and a modern deep-sea rocky substrate, with nothing in between. It is (for a bryozoologist) like finding a living Tyrannosaurus rex with no fossils between them! Above images are from figure 2 of the later analytical paper by Schwaha et al. (2021): (b) colonies attached to the surface of an arenaceous foraminiferan, showing dispersed zooids and thin proximal cystid appendage; (c) a single zooid; (d) the apertural folds — our Pierrella pleated collar! (Abbreviations: ap – aperture, pca/cd – proximal cystid appendage/cd, z – zooid.)

Then came this month’s Song et al. (2026) paper described above, which nearly doubled the depth record of Pierrella to 9981 meters. These authors also used Pierrella as the type genus of a new bryozoan family (Pierrellidae), and they commented on its archaic nature having implications for the evolution of ctenostome bryozoans, a topic also explored by Schwaha et al. (2021). The above images are from Song et al. (2026, fig. S10).

So what explains this extraordinary hiatus between the Cretaceous Pierrella and its living relatives? It is no doubt attributable to the small soft-bodied composition of Pierrella, along with cryptic habitats. The Cretaceous specimens were only found because of rapid fine-grained mineralization that enveloped their colonies shorty after burial. (And that some paleontologists were looking for cryptic fossils inside shells.) Ordinarily Pierrella had little chance of making it into the fossil record. Even the living Pierrella is difficult to see. Song et al. (2026) write that it “was almost invisible and easily overlooked, owing to its transparency and the rough black ferromanganese layers on the rock surfaces that it encrusts”. This is yet another example of how much the fossil record is controlled by the vagaries of preservation.

References:

Grischenko, A.V., Gordon, D.P., and Melnik, V.P. 2018. Bryozoa (Cyclostomata and Ctenostomata) from polymetallic nodules in the Russian exploration area, Clarion-Clipperton Fracture Zone, eastern Pacific Ocean-taxon novelty and implications of mining. Zootaxa, 4484(1), 1-91.

Schwaha, T., Grischenko, A.V., and Melnik, V.P. 2021. Morphology of ctenostome bryozoans: 4. Pierrella plicata. Journal of Morphology. doi: 10.1002/jmor.21344

Song, X., Gooday, A.J., Gordon, D.P., Leduc, D., Sun, Y., Wang, Z., He, Q., Gao, Z., Ruthensteiner, B., Waeschenbach, A. and Schwaha, T. 2026. Protist-dominated hard substrate faunas thrive at the deepest ocean depths. Science, 392(6799), p. 749-754.

Wilson, M.A. and Taylor, P.D. 2012. Palaeoecology, preservation and taxonomy of encrusting ctenostome bryozoans inhabiting ammonite body chambers in the Late Cretaceous Pierre Shale of Wyoming and South Dakota, USA. In: Ernst, A., Schäfer, P. and Scholz, J. (eds.) Bryozoan Studies 2010; Lecture Notes in Earth Sciences 143: 399-412.

 

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