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Devitt, J.

Publications and source records attributed to Devitt, J..

3 recordsLinked to original sources

Airborne DNA reveals synchronized responses of tropical forest assemblages to precipitation

Tropical forests contain much of Earth's biodiversity, yet community-wide responses to seasonal climate transitions remain poorly resolved. We used weekly airborne environmental DNA sampling, supplemented by spatially intensive dry- and wet-season campaigns, to characterize fungi, plants, arthropods, and vertebrates across the dry-to-wet-season transition in a lowland tropical forest. All four assemblages shifted abruptly and nearly synchronously following rainfall late in the dry season, before the meteorological wet season began. These compositional transitions were largely independent of taxonomic richness and airborne DNA concentrations, indicating coordinated changes in detection patterns rather than simple seasonal gains in richness. Across all samples, we recovered more than 5,400 operational taxonomic units, including 2,148 fungi, 857 plants, 2,157 arthropods, and 239 vertebrates. We also recovered 949 full-length insect DNA barcodes, demonstrating compatibility with standard barcoding approaches and expanding opportunities for species discovery. Because the onset of the meteorological wet season showed no long-term trend at Barro Colorado Island, predicting future phenological and compositional shifts will require greater attention to dry-season rainfall variability and the cues that organisms track during this transition. Airborne environmental DNA offers a scalable, noninvasive framework for monitoring biodiversity and phenology across taxonomic groups.

ecology↗

Targeted hybridization capture enables comprehensive detection of freshwater bioassessment invertebrates from environmental DNA

Freshwater bioassessment relies on assessing aquatic assemblages to infer ecological conditions, yet conventional surveys require extensive field sampling, specimen processing, and specialized taxonomic expertise. Existing environmental DNA (eDNA) methods have not yet provided a practical alternative to conventional macroinvertebrate assays in part because current approaches cannot feasibly recover broad taxonomic diversity at sufficient taxonomic resolution. Here, we evaluated targeted hybridization capture of mitochondrial cytochrome oxidase I (COI) target sequences as a unified molecular approach for cross-phylum freshwater bioassessment. Environmental DNA was collected at 18 sites along 63 km of Boulder Creek spanning nearly 1,500 m of elevation from forested headwaters to agricultural plains. COI targets were enriched using custom RNA bait panels designed to target regional freshwater arthropods, annelids, and molluscs. Hybridization capture increased recovery of COI sequences [~]1,760-fold relative to unenriched shotgun libraries, generating Folmer-region COI contigs that averaged [~]400 bp. Across the watershed, we recovered sequences for approximately 450 macroinvertebrate genera across 8 phyla. Detected macroinvertebrate richness averaged 56 genera per site and increased down Boulder Canyon before declining downstream of the city. Macroinvertebrate assemblage composition from hybridization capture paralleled patterns observed with past conventional bioassessment. These results demonstrate that targeted hybridization capture enables robust, cross-phylum detection of species used for freshwater bioassessment from environmental DNA.

ecology↗

Surveying Tropical Faunal Diversity via Airborne DNA Analyses

Here, we assess the potential of airborne eDNA (airDNA) metabarcoding to characterize arthropod and vertebrate assemblages in a tropical forest. We deployed 28 high-flow air samplers across a 1.5 km2 area on Barro Colorado Island, Panama, over two consecutive 24- hour periods and sequenced captured DNA using general eukaryotic and vertebrate-specific metabarcoding primers. AirDNA sampling detected 1293 arthropod operational taxonomic units (OTUs) alongside 157 vertebrate OTUs representing birds, mammals, reptiles, amphibians, and fish. Arthropod richness was comparable to that quantified locally with light and Malaise trap surveys, while vertebrate richness exceeded that typically observed with conventional techniques. The level of field and lab effort employed in this study captured approximately 84% of the asymptotic richness for arthropods and 76% for vertebrates, implying that relatively little additional richness would have been quantified with additional effort within the same domain of sampling. Observed and asymptotic richness increased with the number of sites, the number of days a site was sampled, and the number of PCR replicates run per sample, highlighting the need to standardize effort among future applications of airDNA to compare richness across systems. These results demonstrate that airDNA metabarcoding can efficiently and non- invasively profile tropical terrestrial faunal biodiversity.

ecology↗