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Crayfish, Tributaries & Microplastics: A Reflection on my Internship with Polygone Systems and Willistown Conservation Trust

September 11, 2025 By Watershed Protection Team

By: DeJenae Smith

Living in a densely populated city, the sight of a stray chip bag near a drain or illegally dumped trash is like finding a pebble in cobblestone. But what if there was pollution happening that we couldn’t easily perceive?

Water is one of the world’s largest and most valuable resources, and yet our society’s current structure has a strong reliance on a supply that actively pollutes water bodies – plastics. Just over twenty years ago, the term ‘microplastics’ was first used in a scientific publication and since then, an entire branch of research has since blossomed and exploded. Scientists have researched and found the presence of microplastics in the air, water, soil, and many aquatic and terrestrial organisms – including humans.

Microplastics are defined to be between one and five millimeters in size and are derived from a wide variety of sources. Primary microplastics enter the environment micro-sized, like tire dust or microbeads found in personal care products. Secondary microplastics are from larger plastics being broken down into smaller particles. Both plastic types can easily find their way into our streams and rivers: from directly polluting water with non-biodegradable waste to washing synthetic materials down our drains and sinks through everyday activities. Beyond the direct harm of ingesting microplastics, these materials can also carry harmful chemicals with them, leading to unknown complications for organisms’ wellbeing.

Since April of this year, I have been working alongside Willistown Conservation Trust (WCT) and PolyGone Systems to better understand the contamination of microplastics in our waters and further the advancement of technology for microplastic removal and recovery. After months of planning and development, PolyGone and WCT officially deployed a microplastic-collecting device (affectionately referred to as the ‘Plastic Hunter’) this July in Ridley Creek at WCT’s Ashbridge Preserve. I have been conducting a 9-week study of the microplastics collected over time, along with testing the Plastic Hunter’s performance.

Working with PolyGone, I have gained a lot of experience on the technical component of science, along with developing the skills necessary for an independent researcher. Through their diverse and specialized teams, I have better learned how to better communicate with other scientists, as well as through interdisciplinary channels.

Experimental results that are easily digestible to me may not be the same for an engineer, or even my lab partner – and learning how to translate such information to other people has been a great experience about perspective and its importance of having diversity. As our team worked on the completion of a prototype, it quickly became clear to me how valuable having others present to critique and discuss was, and that aspect played a strong role in the visualization and creation of this year’s Plastic Hunter (Figure 1).

Figure 1. Photographs of the Plastic Hunter established at Ashbridge Preserve (top) and with its filter boxes filled with material as they sit in RIdley Creek (bottom).

Alongside soft skills, I have also developed significantly as an independent researcher and lab technician.

In comparison to my research experiences in a college-setting, I have had much more autonomy and played an important role in the designing of my research project and collection of data. As the current Plastic Hunter has gone through design changes from previous years, I encountered many new challenges, often having to find creative solutions and work-arounds (Figure 2).

Figure 2. A collected filter box brought into the lab for further processing, taped with a sample identifier (top). In an attempt to minimize external exposure with plastics, each box is stored inside of a plastic-free compostable bag (bottom).

While working on a separate project, I was also considered a valued lab member and thus became very familiar with the space and how to conduct key tasks and operate equipment. After the departure of my fellow interns for the school year, I now frequently manage the lab space on my own as I complete the day’s given experiments or sample processing (Figure 3, Figure 4, Figure 5).

Figure 3. The aftermath of washing a filter box before (left) and after (right) adding hydrogen peroxide to dissolve organic materials in the water.
Figure 4. Photographs running the peroxide-digested water through a filter paper (left) and staining the sample with the chemical Nile Red. As plastics are dyed, they can be seen under a powerful microscope.
Figure 5. Photograph of a fully processed water grab sample in a petri dish, ready for imaging under our microscope (top). Using our imaging protocol, the microscope snaps a picture of a very small area of the petri dish (which can be up to 8,000 photographs total!), stitching them together to generate three image versions of the sample (bottom). With programming, a computer can analyze the sample and estimate the total number of microplastics present.

While I work on my technical skills in the lab with PolyGone, it is with WCT that I am able to effectively apply and adapt my approach in the environment, which has undoubtedly been the best part of my co-op experience. Where one may precisely model and predict results in the lab, I enjoy having each of those expectations wiped-out by the inconsistencies and unpredictably inherent to the natural world.

Being mentored by Lauren McGrath, Anna Willig, and Sarah Barker of the Watershed Team, alongside the wonderful individuals in other WCT departments, I have started to comprehend the true multidimensionality that is our environment. Alongside conducting water chemistry and analysis, I have learned much about Pennsylvania’s and the world’s natural history, from environmental justice to case studies in wetland ecology. As I approach the end of my co-op and enter my junior year, this internship has truly been a transformative experience for me. Before, I used to focus solely on the analytical component to science and research, but my internship with PolyGone and WCT has drastically changed that view for me. As I continue my education and grow as a professional, I now aspire to become a naturalist alongside a scientist. Instead of taking from the environment for the sake of my research, I wish to connect deeper with natural landscapes and use my results in pursuit of palpable change to conserve and improve the state of our water, air, and biota (Figure 6).

Figure 6. A collection of the life found at Ashbridge Preserve (A: Painted Turtle [Chrysemys picta] , B: A fawn and its mother, C: A baby Snapping Turtle [Chelydra serpentina)], a female Blackburnian Warbler [Setophaga fusca] banded at Rushton Conservation Center by the Bird Team (D), an empty Eastern elliptio [Elliptio complanata] mussel shell found in Darby Creek during mussel surveying (E).

References

How Do Microplastics Enter The Environment?. (2022, January 28). Ocean Diagnostics. Retrieved August 15, 2025, from https://oceandiagnostics.com/ocean-diagnostics-blog/post/how-do-microplastics-enter-the-environment

Issac, M. N., Kandasubramanian, B. (2021, March 2). Effect of microplastics in water and aquatic systems. Environ Sci Pollut Res, 28(16), 19544 – 19562. https://doi.org/10.1007/s11356-021-13184-2

Kye, H., Kim, J., Ju, S., Lee, J., Lim, C., Yoon, Y. (2023, March). Microplastics in the water systems: A review of their impacts on the environment and their potential hazards. Heliyon, 9(3). https://doi.org/10.1016/j.heliyon.2023.e14359

Lai, C. (2022, July 20). Microplastics in Water: Threats and Solutions. Earth.org. https://earth.org/microplastics-in-water/

Microplastic Contamination: Sources, Effects, and Solutions. (2025, August 1). Biology Insights. Retrieved August 15, 2025, from https://biologyinsights.com/microplastic-contamination-sources-effects-and-solutions/

Savchuk, K. (2025, January 29). Microplastics and our health: What the science says. https://med.stanford.edu/news/insights/2025/01/microplastics-in-body-polluted-tiny-plastic-fragments.html

Targhan, H., Evans, P., Bahrami, K. (2021, December 25). A review of the role of hydrogen peroxide in organic transformations. Journal of Industrial and Engineering Chemistry, 104, 295-332. https://doi.org/10.1016/j.jiec.2021.08.024

Thompson, R.C., Courtene-Jones, W., Boucher, J., Pahl, S., Raubenheimer, K., Koelmans, A.A. (2024 September 19). Twenty years of microplastic pollution research – what have we learned?. Science, 386(6720). doi: 10.1126/science.adl2746

Types of Pollution. (n.d.). Science Facts. Retrieved August 14, 2025, from https://www.sciencefacts.net/types-of-pollution.html

Water Quality and the Global Microplastic Crisis. (n.d.). Safe Piping Matters. Retrieved August 14, 2025, from https://safepipingmatters.org/2019/03/20/water-quality-and-the-global-microplastic-crisis/

Yale Experts Explain Microplastics. (2020, December 1). Yale Sustainability. Retrieved August 13, 2025, from https://sustainability.yale.edu/explainers/yale-experts-explain-microplastics

Yee, M.S., Hii, LW., Looi, C.K., Lim, WM., Wong, SF., Kok, YY., Tan, BK., Wong, CY., Leong, CO. (2021 February 16). Impact of Microplastics and Nanoplastics on Human Health.  Nanomaterials, 11(2), 496. https://doi.org/10.3390/nano11020496

Filed Under: Uncategorized

A Love Letter to the American River Otter

June 14, 2025 By Watershed Protection Team

By: Lauren McGrath

American river otters (Lontra canadensis) are a highly sensitive and beautiful stream resident. Known for their charismatic personality and cartoonishly adorable faces, these adorable predators play an important role in managing aquatic ecosystems as well as showcasing ecosystem health.


River otters range from about 2.5 to 5 feet in length, and can reach weights up to 33 pounds. In the weasel family, (scientifically known as the mustelid family), otters have a long, muscular body, streamlined for swimming, with short legs and webbed feet and are apex predators in stream ecosystems. With a rapid metabolism, river otters need to eat frequently and their small, square skull is heavily muscled, allowing them to rapidly snap their jaws around their fast moving prey while underwater.

An adorable wet North American river otter wandering in shallow water

River otters are highly sensitive to changes in water chemistry, making it a valuable indicator species for aquatic ecosystem health. As a top predator in freshwater environments, river otters depend on clean, well-oxygenated water to support their diverse diet, which includes fish, mussels, clams, crayfish, crabs, frogs, birds’ eggs, birds and reptiles such as turtles. Changes in pH, dissolved oxygen, and nutrient levels can affect prey availability and disrupt the delicate balance of the aquatic ecosystems otters inhabit. Additionally, pollutants, such as heavy metals, pesticides, and industrial runoff, can bioaccumulate in their bodies through the food chain, leading to health issues including reproductive problems and organ damage leading to population declines. Because of their dependence on high-quality water, even subtle chemical shifts can impact otter populations, highlighting the importance of restoring and maintaining clean waterways for their survival. 

In addition to being indicators of healthy ecosystems, river otters play an important role in the environment. River otters are a keystone species in aquatic ecosystems: as a predator, they regulate prey populations, their foraging and den building behaviors modify habitat structure for other wildlife, and their presence in the ecosystem influences community dynamics. Most importantly, they serve as indicators of ecosystem health, and contribute to overall biodiversity and ecosystem resilience. Protecting and conserving otter populations and their habitats is essential for maintaining the ecological balance and functioning of freshwater ecosystems.

These incredible animals were present in most waterways across North America prior to the arrival of European settlers. As a result of trapping for their valuable pelts, habitat destruction, and widespread declines in healthy ecosystems due to human development, river otters disappeared from waterways across most of Pennsylvania by the early 1900’s, however focused reintroduction efforts in the 1980s led to a population rebound in northern Pennsylvania. Currently, river otters are protected in Pennsylvania.

In 2023, river otters were documented in the headwaters of Ridley Creek in southeastern Chester County. It was the first time they had been documented in this waterway in over 100 years. There are known populations further west in Chester County, notably in the Brandywine watershed. The arrival of these highly sensitive animals is an indication that the work of Willistown Conservation Trust and other local conservation and watershed organizations throughout the region has provided space for sensitive wildlife, such as otters, to return. Continued monitoring of water quality will ensure that we maintain the high standards that these incredible animals need to thrive!

Funding for this project was awarded through the “Protect Your Drinking Water” grant program, administered by the Pennsylvania Environmental Council with funding from Aqua, an Essential Utilities company.

Filed Under: Uncategorized

Testing the Waters (Literally!) of a Water Chemistry Career

June 13, 2025 By Watershed Protection Team

By: Lauren Carroll

Hello and happy Creek Week! My name is Lauren Carroll, and I am a senior at Conestoga High School. During May of our senior year, we are given the opportunity to intern at an external non-profit or company in a field of interest/our major in college. I am lucky enough to be doing my internship with the Watershed Department here at the Willistown Conservation Trust! During this month I have learned so much about work after graduating high school, as well as our earth. I have been able to learn so much so fast, partially because of how much time we spend out in the field. 

For example, I, along with a fellow intern, Clare, and our supervisor, Anna, performed a mini-stream study on the upstream Ashbridge sensor area. This study was conducted in hopes of finding out why the sensor station located in Ridley Creek was reading high levels of conductivity. Conductivity is the measure of how easily electricity can move through water. To begin the mini-study, we first made a map (Map 1) and chose 13 sites of interest to sample. We made sure to choose sites in the mainstream of Ridley Creek, in the outflow of the wastewater tributary, where these waterways meet, downstream, and on the various parts of the left and right stream banks. At each of these sites we collected 125 mL bottles of water and also recorded the temperature of the water, the time we took the sample and the conductivity of the water in that specific location. 

Later, in the lab, we tested chloride levels, which relate to conductivity, as well as nutrient levels such as nitrates and nitrites at select sites.  This is because there is a wastewater treatment plant that deposits water into this stream from a tributary, and we know wastewater typically contains high levels of nutrients and has higher conductivity as well. These nutrients are harmful to the overall health of our streams in abundance.  The word nutrients may sound positive, but it actually is not. They cause, in excess, an event called eutrophication, which is extreme plant growth, most often algae. This causes dissolved oxygen levels to decrease, which harms aquatic life. Mass fish die-offs can occur because they are suffocated. Interestingly, while we were in the creek taking samples, we could see the difference between the right bank and the left bank’s algae growth due to the nutrients carried by the wastewater tributary. The right bank was brown, and the left bank was a vibrant green which shows this difference in algae growth. 

Learning how to take water samples properly, measure conductivity in the field, record data, perform tests for chloride and nutrients in the lab and interpret the data has been such a beneficial experience. Throughout my internship, I have also been able to learn about other fascinating things going on in our waterways that are less chemistry-focused, such as taking a look at our Freshwater Mussel population and seeing their effect on water quality as well as their use as an indicator species. Another animal that can be used as an indicator species is the River Otter. When you see freshwater mussels and otters in a stream, you know it is happy and healthy! 

Overall, I have loved looking at our waterways through all the different lenses, from things as small as a molecule of NO3 to as large as an Otter! I have learned so much about how everything interacts and balances each other out, as well as how to help our waterways to be healthier and happier. I hope you learn just as much this week as I have and can help us keep our waterways healthy and happy!

Funding for this project was awarded through the “Protect Your Drinking Water” grant program, administered by the Pennsylvania Environmental Council with funding from Aqua, an Essential Utilities company.

Map 1. Sample site locations 
Sample sites 2 and 3 are in the wastewater tributary, and 4 is at the confluence of Ridley creek and the tributary. Sample sites 5 and 8 are on the right bank. Sample sites 6 and 8 are in the center of the stream. Sample site 7 is on the left bank and is our PURC1S sensor.

Filed Under: Uncategorized

Reading the Riparian Zones: What Trees Reveal About Watersheds

June 12, 2025 By Watershed Protection Team

By: DeJenae Smith

If you want insight on the health of a body of water, having a laboratory or expensive equipment is not a necessity. Often, all you have to do is look up – not at the sky or its clouds, but at the trees. Unlike migrating birds, fish, or other highly mobile organisms, trees stay rooted in one place, living alongside or near a stream, creek, or river for as long as the water flows, and often for many centuries after. Their presence, structure, and diversity can offer powerful information about the health of a watershed.

Over the past few months that I’ve spent as a Drexel University co-op with WCT, I have learned a lot about the process of ‘reading the landscape’ and its value; and I quickly realized how much of that understanding depends on trees.

While trees serve many functions for an ecosystem and planting more in a space is beneficial, it is important to plant a tree in the appropriate conditions to increase their chances of survival. As I’ve walked through Kirkwood and Ashbridge Preserves and participated in riparian tree plantings, I have learned from my mentors about three key “zones” for trees and shrubs as it relates to wetlands.
Zone 1 is located closest to the stream’s edge. Examples of trees WCT has planted here are silver maple (Acer saccharinum), buttonbush (Cephalanthus occidentalis), American sycamore (Platanus occidentalis), and swamp white oak (Quercus bicolor) (Figure 1). These species are very tolerant to wet soils and are key in keeping a stream bank together (Figure 2).

Figure 1. Examples of Zone 1 trees.
Figure 2. An example of heavy erosion along the River Swale in Yorkshire, England. While erosion is a natural process, this issue can be much more destructive without the strong, deep roots of Zone 1 trees to hold soil together, especially during flood events. (Soil-net)

Alongside structural support, trees in Zone 1 provide other functions. As they grow and create canopies, they provide shade over a water body, keeping the water cool for fish and invertebrates. Trees are also capable of cladoptosis, the process of shedding their branches. When branches fall into water, they can provide habitat, hiding places, or transportation for small aquatic organisms (Figure 3).

Figure 3. Smaller organisms like these turtles can use branches for easier travel across water, avoiding potential predators, or for soaking up the sun’s rays. (Pxhere)

About 15 feet from the water is Zone 2, also known as the “Transitional Zone.” Trees here are tolerant of moist conditions, but not to the same extent as plants in Zone 1. The primary purpose of trees and shrubs in this area is to absorb excess nutrients and potential contaminants, preventing them from entering the water.

Examples of trees that thrive in this zone are chokeberry (Aronia melanocarpa), redbud (Cercis canadensis), and pin oak (Quercus palustris). A densely populated forest offers more habitats and food sources, also acting as a rest stop for migrating birds.
Figure 4. Examples of Zone 2 trees and shrubs.

Going even further, Zone 3 is located about 50 feet from the water, typically contains fewer large trees and is full of native grasses, shrubs, and wildflowers. Plants in Zone 3 are the first line of protection for the stream, filtering runoff that may carry sediment, nutrients, or pesticides. Zone 3 also helps prevent flooding. When there’s heavy rain,  stormwater can rush into a watershed at once. Dense vegetation in Zone 3 slows that water before it reaches lower zones. As water takes longer to travel, more of it soaks into the soil and helps refill the groundwater supply. 


Groundwater is essential for drinking, farming, and keeping land stable. If too much is removed, the ground can sink – a problem called subsidence. Zone 3 plants help prevent this by allowing rainwater to seep into the ground. Some of the shrubs WCT has added here include red osier dogwood (Cornus sericea), witch hazel (Hamamelis virginiana), and common ninebark (Physocarpus opulifolius).

Figure 5. Examples of Zone 3 shrubs.

Each layer of the riparian zone plays a unique and vital role in keeping our watersheds healthy. While these areas may seem like simple scenery, the trees, shrubs, and plants that grow there work hard to stabilize streambanks, filter pollutants, support wildlife, and show us the health of our watersheds. Learning to read these green spaces during my time with WCT has deepened my appreciation for the overlooked power of riparian zones and the trees that stand not in stillness, but in silent service to the land and its ecosystems.

Funding for this project was awarded through the “Protect Your Drinking Water” grant program, administered by the Pennsylvania Environmental Council with funding from Aqua, an Essential Utilities company.

References

‌Multifunctional Riparian Forest Buffers: More Than Just Trees. (n.d.). Extension.psu.edu. https://extension.psu.edu/multifunctional-riparian-forest-buffers-more-than-just-trees

‌Penn State Extension. (2005, February 11). Riparian Buffers for Wildlife. Penn State Extension. https://extension.psu.edu/riparian-buffers-for-wildlife

Plant Materials | Natural Resources Conservation Service. (2024, March 7). Www.nrcs.usda.gov. https://www.nrcs.usda.gov/plant-materials

Riparian Tree Plantings – Western Pennsylvania Conservancy. (2023, October 20). Western Pennsylvania Conservancy. https://waterlandlife.org/trees/riparian-tree-plantings/

‌Trees, Shrubs, and Groundcovers Tolerant of Wet Sites. (2022). Psu.edu. https://extension.psu.edu/trees-shrubs-and-groundcovers-tolerant-of-wet-sites‌US Department of Commerce, National Oceanic and Atmospheric Administration. (2019). What is subsidence? Noaa.gov. https://oceanservice.noaa.gov/facts/subsidence.html

Filed Under: Watershed

Secrets of a Photosynthetic Powerhouse: Diatoms in Detail

June 11, 2025 By Watershed Protection Team

As a continuation of our previous blog post all about the wonderful world of microalgae, this piece will provide a more in-depth profile on the most important member of freshwater algal communities, diatoms. If you have not had a chance to read the first part of this series, it may be helpful in providing background information and context for this post.

It takes a whole lot of energy to satisfy all the wildlife in aquatic and marine ecosystems. While the most well known photosynthesizers may be terrestrial plants like trees and shrubs, some of the most significant and unusual primary producers on the planet are thriving in local creeks! These underrepresented microbes are called diatoms, a kind of photosynthetic microscopic algae. 

When it comes to photosynthesis diatoms are the heavy-weight aquatic champions! Whether they are floating blissfully through the Pacific Ocean, stuck to the leaf of a cattail within a wetland or covering large rocks on the bottom of a riverbed, diatoms are the most proficient primary producers in our waters. They provide between 20-40% of the oxygen available on earth and are the most important member of the base of the freshwater food chain, making up the vast majority of plant matter for grazing animals to feed on from zooplankton to large fish. 

Diatoms occupy a very unique position among microalgae, they are the most recently evolved group of algae and therefore, benefit from specialized traits that are not present in other taxa. Diatoms, like all microalgae, are incredibly sensitive to shifts in water chemistry or weather events. However, they have evolved tough cell walls made out of silica (the same material used to make glass) called frustules. This adaptation makes diatoms much more physically resilient than their neighbors and allows them to literally “weather the storm” while other algal cells comprised of cellulose and pectin may be destroyed; this also makes them better armored against infection and predation.

In addition, diatoms employ several different strategies for movement and reproduction depending on the species – as a rule of thumb more diversity within a group provides a greater likelihood of someone succeeding even if it isn’t the whole community. If one strategy fails, another may be more environmentally advantageous; in nature it often pays off to hedge your bets.

Some species of diatom like this Gomphonema form colonies attached to a substrate even though they also have two raphes.

Depending on just how recently a species of diatom has evolved, there are several different life paths they can take. The most ancient or ancestral species are planktonic, meaning they cannot move independently of the water’s current. The most newly evolved species (called novel or derived species) can permanently attach themselves to a surface using an excreted glue-like mucus and/or use one or two specialized openings in their frustule called raphes to propel themselves through the water.

The photo to the left shows an ancient, planktonic species of diatom called Stephanocyclus meneghinianus while the photo to the right shows several more novel, raphe-equipped species including Gyrosigma reimeri in the center and a few Planothidium frequentissimum cells. (Photo credit: https://diatoms.org/species/48640/stephanocyclus_meneghinianus)

Another strange superpower of diatoms is their ability to “hibernate” for prolonged periods of time while buried in sediment. If environmental conditions become unbearable, or high flow blasts diatoms off of their substrate they can simply settle into the stream bed where they become inactive until another forceful current comes along to disturb them from their slumber or conditions become more favorable. This ability is moreso an adaptation as a consequence of their silica cell walls, as they are quite heavy and can cause the entire cell to sink.

In a very vampiric twist, some diatoms can remain inactive in this dormant state for as long as 7,000 years while still being able to resume function according to one 2025 study (Bolius et al., 2025). Diatom reproductive strategy only adds to the immortality rumors – they almost exclusively reproduce asexually, but because of the rigid silica of their cell walls each daughter cell is smaller than the parent. Therefore, the older the diatom, the smaller the cell. Each daughter receives one half of their frustule from the parent and grows one half itself, leaving the parent to grow another half as well, with each resulting cell being both genetically and physically identical.

These tiny plants are generous and full of fascinating mysteries, the depths of which we are only now starting to unearth. Thanks to all their eclectic adaptations diatoms have certainly earned MVP status for habitats worldwide! 

Funding for this project was awarded through the “Protect Your Drinking Water” grant program, administered by the Pennsylvania Environmental Council with funding from Aqua, an Essential Utilities company.

References:
Behrenfeld, M. J., Halsey, K. H., Boss, E., Karp‐Boss, L., Milligan, A. J., & Peers, G. (2021). 
Thoughts on the evolution and ecological niche of diatoms. Ecological Monographs, 
91(3). https://doi.org/10.1002/ecm.1457 

Bolius, S., Schmidt, A., Kaiser, J., Arz, H. W., Dellwig, O., Karsten, U., Epp, L. S., & Kremp, A. 
(2025). Resurrection of a diatom after 7000 years from anoxic Baltic Sea Sediment. The 
ISME Journal, 19(1). https://doi.org/10.1093/ismejo/wrae252 

Stevenson, R. J., Bothwell, M. L., & Lowe, R. L. (2008). Algal ecology: Freshwater benthic 
ecosystems. Academic Press.

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