Optimizing eDNA sampling: Which filters best capture marine biodiversity?

$5,490
Raised of $4,393 Goal
124%
Funded on 11/01/25
Successfully Funded
  • $5,490
    pledged
  • 124%
    funded
  • Funded
    on 11/01/25

About This Project

Recent trials in the Galapagos demonstrate that environmental DNA (eDNA) is a powerful biodiversity monitoring tool. This project compares PUF filters (emerging technology) and cellulose membranes (industry standard) using diver-towed devices at four sites in Monterey Bay National Marine Sanctuary. One filter will emerge from the trial as having outperformed the other in capturing biodiversity, enabling the development of standardized marine eDNA monitoring protocols.

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What is the context of this research?

eDNA is transforming how we monitor marine biodiversity, often outperforming traditional surveys in efficiency and species detection. Comparative studies show that eDNA can detect cryptic taxa missed by visual or BRUV surveys while also being more cost-effective. Yet methodological choices, especially filter type, strongly influence DNA recovery. Recent comparisons of eDNA collection confirm that filter material alone can shift DNA composition. Novel approaches, including the use of paint rollers for submerged surface sampling, highlight the rapid pace of experimentation in the field. This project compares emerging and established substrates, polyurethane foam and cellulose, under identical conditions in Monterey Bay, to evaluate which will yield the most species detections when processed through standard sequencing protocols. The results will improve the accuracy of marine eDNA surveys, strengthen open biodiversity databases, and inform methods for reliable, long-term monitoring.

What is the significance of this project?

eDNA is strengthening our ability to understand the natural world by generating vast amounts of biodiversity data quickly and economically. In California, eDNA studies in Scorpion State Marine Reserve and across the Channel Islands are already informing marine protected area (MPA) monitoring, supporting climate change assessments, and sustainable fisheries management. But eDNA results are only as reliable as the methods used to collect them. As the technology has spread, protocols have lagged, creating inconsistent and less reliable data, particularly in marine environments. This project addresses that gap by directly testing how filter choice influences species detection, improving confidence in eDNA as a tool to protect biodiversity. Highlighting the urgency of the extinction crisis, this work also stresses the scale of opportunity that big data brings to policy impact, and shows real-world relevance by strengthening the evidence base for designating and enforcing protections.

What are the goals of the project?

The funds will be used to purchase diver-towed sampling devices with flowmeter, 3D-printed cellulose filter adapters, and filters, and to cover sequencing costs at Jonah Ventures lab. Four divers will collect samples at Breakwater, Lover’s Point, Whaler’s Cove, and Monastery in Monterey Bay. At each site, two divers will tow polyurethane foam filters and two will tow cellulose filters, yielding 16 total samples. Filters will be preserved in DNA buffer, shipped to the lab, and sequenced using standard metabarcoding protocols. After the return of the raw data, we will analyze it against known species lists to compare biodiversity detection across filter types. The study will be carried out in fall 2025, with sequencing completed within six weeks. Results will be deposited in GenBank for open access and written up for peer-reviewed publication, providing the research and conservation community with clearer methods for reliable marine biodiversity monitoring.

Budget

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This budget covers just the essentials needed to collect and analyze eDNA in Monterey Bay. The biggest cost is sequencing ($2,080), carried out by our partner lab Jonah Ventures in Colorado, which will tell us what species are present in the samples. The tow devices ($1645 ) are a one-time equipment cost — the original prototypes were left in the Galápagos as a donation to Darwin Station researchers, so we need to acquire a second set for California trials. We’ll compare two filter types (PUF $112; cellulose $64), with preservative ($125) and tubes ($25) to keep the DNA collected in the filters stable until analysis. Scuba tank fills ($192) and shipping ($50) cover basic logistics. Importantly, all dive time and analysis is donated by volunteers — shown as an in-kind contribution of $0 — keeping the focus on lab and materials costs. This streamlined budget represents the minimum needed to complete the project.

Endorsed by

I strongly endorse Christina Biggs’ project comparing eDNA filter substrates in Monterey Bay. During our work together at Monterey Bay Aquarium, Christina developed innovative aquaculture systems and demonstrated both technical expertise and leadership as a mentor. Her unique ability to bridge engineering, biology, and conservation makes her exceptionally well qualified to lead this important study on advancing eDNA monitoring methods.
I fully endorse Christina Biggs' eDNA project. Our seahorse research collaboration showcased her exceptional expertise in marine biodiversity and innovative sampling methods. Her proven field experience and creative problem-solving skills make her an ideal candidate to lead this critical work in developing standardized eDNA protocols for global conservation. I have complete confidence in her success.

Project Timeline

Equipment will be purchased by Oct 1, 2025. Field sampling at four Monterey Bay sites will take place over two weeks in early November 2025. Sequencing results from Jonah Ventures are expected by mid-January 2026, with data analysis completed by March. A manuscript will be prepared and submitted by June 1, 2026, with all data released via GenBank.

Oct 01, 2025

Equipment purchased and prepared for fieldwork

Oct 02, 2025

Project Launched

Nov 01, 2025

Dive 1 Breakwater

Nov 02, 2025

Dive 2 Lovers Point

Nov 08, 2025

Dive 3 Monastery

Meet the Team

Christina Biggs
Christina Biggs

Christina Biggs

Christina Biggs is a marine ecologist, expedition leader, and conservation strategist with over 20 years of experience advancing biodiversity discovery. She has directed more than 50 expeditions worldwide, from deep-sea ROV surveys in Monterey Bay to biodiversity assessments in Africa, Indonesia, and the Americas.

As Exploration Director at Re:wild, Christina designed and led the organization’s Search for Lost Species, curating a 4,500-species list with IUCN specialists, and overseeing dozens of rediscoveries. She co-chaired the IUCN SSC Lost Species Task Force and the Specimen Collection Policy Council, advised the IUCN Biodiversity Assessment Unit on integrating eDNA data into Red List assessments, and served on the Technical Council of ReShark.

Previously, Christina was Senior Researcher at the Monterey Bay Aquarium/Research Institute, where she was Chief Scientist on deep-sea missions aboard the R/Vs Western Flyer and Rachel Carson, documenting undescribed invertebrates, mapping seafloor habitats, and helping design the $17M Into the Deep exhibit. At Shedd Aquarium, she advanced cephalopod aquaculture and reef monitoring across the Bahamas and U.S. East Coast.

Her publications span Frontiers in Ecology and the Environment, Global Change Biology, Animal Conservation, Environmental DNA, and the Journal of Marine Science and Engineering. She has been an invited speaker at the World Species Congress, the Society for Integrative and Comparative Biology, and the Shark Conservation Fund.

A National Fellow of The Explorers Club, Christina carried a Flag on her 2025 Galápagos expedition that confirmed the rediscovery of a lost coral and piloted new diver-towed eDNA collection methods. She continues to lead cutting-edge biodiversity projects as a consultant with RIDGES Foundation.

Additional Information

In summer 2025 we piloted this approach in the Galápagos, pairing diver-towed filtration with an automated sampler. However, the two systems used different substrates: polyurethane foam in the tow and cellulose membranes in the automated unit. Since cellulose is known to sequence more easily, the results are not directly comparable. This Monterey study resolves that limitation by testing the same diver-towed method with both filter types. We have designed a bespoke 3D-printed sleeve to retrofit cellulose filters into the tow device, allowing true side-by-side comparisons. Another challenge in the Galápagos was that the tow device lacked flowmeters and we could not record water volume filtered, while the automated sampler collected a fixed 50 L. To address this, the Monterey devices will be retrofitted with integrated flowmeters, providing a valuable benchmark for comparative studies. These results from the Monterey study will also be integrated as a supplement into the forthcoming Galápagos paper.

Photos:
1. Divers utilizing a passive tow eDNA sampler, similar to what will be used in Monterey Bay.

2. Tow device, cellulose membranes, and polyurethane foam filters—the substrates being directly compared in this study.

3. Monterey Bay kelp forest, a sample site where this project will collect eDNA samples.

4. Preparing tow equipment, filters, preservatives, and metadata sheets for eDNA sampling in the Darwin Station lab—protocols that will also be followed for the Monterey project.


Project Backers

  • 16Backers
  • 124%Funded
  • $5,490Total Donations
  • $343.13Average Donation
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