Graduation Date

Spring 2026

Document Type

Thesis

Program

Master of Science degree with a major in Natural Resources, option Fisheries

Committee Chair Name

Andrew Kinziger

Committee Chair Affiliation

Cal Poly Humboldt Faculty or Staff

Second Committee Member Name

Andre Buchheister

Second Committee Member Affiliation

Cal Poly Humboldt Faculty or Staff

Third Committee Member Name

Darren Ward

Third Committee Member Affiliation

Cal Poly Humboldt Faculty or Staff

Keywords

Environmental DNA, Desiccation, Smith-Root, Hatchery, Estuary, Rainbow trout, Tidewater goby

Abstract

This study investigates the effectiveness of self-preserving filter packs (filters designed to passively dry and stabilize captured eDNA without liquid preservatives or cold-chain) in maintaining the integrity of environmental DNA (eDNA) under varying temperature and environmental conditions. eDNA degradation was assessed at three temperatures (23, 33, and 43 °C) using water collected from two distinct study sites that differ in species composition and salinity, a freshwater hatchery and a brackish lagoon. To capture early degradation dynamics, eDNA concentrations were quantified using quantitative PCR assays immediately after filtration (t = 0) and after 2, 4, 8, 16, 32, and 64 days of storage. Decay dynamics in eDNA concentration were evaluated using candidate survival/decay models. Model selection supported nonlinear decay, with biphasic dynamics frequently top-ranked and consistently competitive, indicating a rapid early loss fraction (f = 0.82–0.97) followed by slower decay fraction, with most loss occurring within the first 4 days of storage. Formal within-site model comparisons indicated minimal temperature influence on concentration-based decay dynamics in hatchery samples, whereas temperature effects were supported in the low-concentration Big Lagoon dataset. Detection results showed a clear and operationally important temperature dependence in the low-concentration Big Lagoon setting: per-sample detection remained 100% through day 32 at 23 °C and through day 16 at 33° C, but declined rapidly at 43 °C (≤70% by days 4–8 and 20% by day 16). These results emphasize that the largest loss of eDNA occurs rapidly after filtration in self-preserving filters, and that warm storage can substantially reduce detection success in low-abundance field samples. Self-preserving filters nonetheless retained high detectability for weeks under moderate heat exposure (e.g., 100% detection at 33 °C through day 16), supporting their use for eDNA monitoring while highlighting the importance of minimizing sustained high-temperature exposure.

Citation Style

AFS

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