Hyperspectral characterization of carotenoid- and retinal-producing halophiles

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About This Project

Hypersaline lakes contain valuable pigment-producing microbes, but mapping them requires extensive sampling. We ask whether drone-based hyperspectral imaging can identify these communities from their unique light signatures. We hypothesize that pigment signatures will predict microbial composition when validated with DNA sequencing and environmental data. This study could enable rapid, noninvasive mapping of Great Salt Lake microbial diversity.

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What is the context of this research?

Hypersaline lakes host microorganisms called extremophiles that thrive in conditions such as intense sunlight, low oxygen, and extreme salinity that are lethal to most life. Many produce colorful pigments that protect them from sunlight or help them convert light into energy. These include bacterioruberin and bacteriorhodopsin from salt-loving microbes called haloarchaea, along with other potentially valuable pigments produced by Dunaliella algae and Salinibacter bacteria (Rodrigo-Baños et al., 2015). Because these pigments interact with light in distinct ways, they may act as optical “fingerprints” detectable by imaging instruments (Wurtsbaugh et al., 2017). We hypothesize that visible and near-infrared (VNIR) imaging, which measures reflected light beyond what the human eye can see, can be combined with DNA sequencing and environmental measurements to predict which pigment-producing microbes are present and enable large-scale monitoring of the lake.

What is the significance of this project?

This project advances four edges. Scientifically, it establishes drone-based hyperspectral imaging as a quantitative method for resolving carotenoid and retinal chromophore distributions in microbial communities, bridging the gap between destructive sampling and coarse satellite remote sensing. Ecologically, it produces a spatially-resolved baseline of Great Salt Lake halophile community structure at a critical moment — the lake has lost roughly two-thirds of its surface area since 1850, threatening these communities before they have been comprehensively characterized. Biotechnologically, the ML classifier framework enables rapid identification of microhabitats enriched in commercially relevant carotenoids and retinal proteins used in antioxidant, cosmetic, and optogenetic applications. Methodologically, this transfers directly to other extremophile systems, providing infrastructure for spatial microbial biogeography.

What are the goals of the project?

This project will deploy a calibrated drone-mounted visible and near-infrared (VNIR) hyperspectral imaging system to collect centimeter-scale data across hypersaline environments. At 30 sites spanning salinity and microhabitat gradients in Great Salt Lake’s North Arm, including Rozel Point and an industrial pond complex, aerial imagery will be paired with shotgun metagenomic sequencing and high-performance liquid chromatography (HPLC) pigment measurements. These data will be used to develop and validate models that estimate bacterioruberin, bacteriorhodopsin, and accessory carotenoid abundance from spectral imagery. Finally, we will create an open-source machine-learning platform that integrates spectral, genomic, pigment, and environmental data to map microbial biogeography and evaluate whether taxonomic composition and functional genes can be predicted from hyperspectral measurements.

Budget

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The imaging hardware (VNIR pushbroom scanner, calibration optics, PTFE white reference) provides the core measurement platform for acquiring spatially-resolved hyperspectral cubes of carotenoid and retinal chromophore signatures. The aerial platform (drone, scanning tripod, calibration tarps) enables low-altitude data collection across the spatial scales needed to capture community heterogeneity in Great Salt Lake brine systems. Field campaign costs (travel, sterile sampling supplies, lodging) directly deliver paired hyperspectral cubes and biological samples at Rozel Point and operator-pond sites. Sequencing and HPLC pigment-extraction costs provide the metagenomic and biochemical ground truth required to train and validate the spectral classifier, which without paired ground truth, the imaging data cannot be quantitatively interpreted. Depending on funding, wet lab biology can take place as described, otherwise it is a stretch goal for another time when funding is acquired.

Endorsed by

This project presents a fantastic opportunity not only to conduct ecologically relevant studies on commercially relevant microbial species in the wild, but also to establish a measurement platform/technology that is directly transferable to other systems.
I worked with Bryan in a previous role at Juno Therapeutics and can attest to his scientific curiosity and tenacity. This project is an excellent opportunity to bridge important questions in biology, spectral imaging, and image processing/machine learning. Bryan is the right person to span these disciplines and answer these questions.

Project Timeline

During weeks 1–4, we will secure permits, build and calibrate the imaging system, and test pigment standards. In weeks 4–6, we will collect paired imagery and biological samples at 30 Great Salt Lake sites. Weeks 6–10 will cover sequencing, pigment analysis, image processing, and model development. A held-out field campaign in weeks 10–11 will validate the models, followed by an open release of data, code, and results in week 12.

Jul 31, 2026

Permits, FAA cert, bench validation, and UAV build

Jul 31, 2026

Project Launched

Aug 14, 2026

Submit samples for sequencing

Aug 14, 2026

Images pre-processed and data engineering begins

Aug 17, 2026

GSL Field Campaign over two weekends, 30 samples

Meet the Team

Bryan Duoto
Bryan Duoto

Bryan Duoto

Bryan Duoto is a hybrid machine learning engineer and wet-lab scientist with research and engineering depth spanning biomedical engineering, synthetic biology, drug discovery, and microbial bioprospecting. He holds a PhD in Biomedical NanoEngineering and an MS in Data Science and Engineering from UC San Diego (2025), an MS in NanoEngineering from UCSD (2022), an MS in Molecular and Cell Biology from Stanford and San José State University (2018), and a BS in Biology from Sonoma State University.

Previously, as the Founder of Embark Bio, he developed CHEMzyme — a conditional protein language model for controllable generation of artificial enzymes from user-specified catalytic reactions — and partnered with Death Valley to source extremophilic microbial samples for training genomic and enzymatic language models. He was an Entrepreneur-in-Residence at the Allen Institute for AI. His work appears in Science, Science Translational Medicine, Cell Reports, Chemical Science, and Scientific Reports.

Lab Notes

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Additional Information

This project is structured for rapid validation and de-risking. All data, calibration files, and analysis code will be released under an open license following publication, contributing a community reference standard for halophile hyperspectral characterization. The hardware design follows a modular open-source pushbroom architecture, supporting replication by other research groups at sub-$2,000 instrument cost. Depending on funding this could be upgraded to a Specim FX10e which would provide better resolution. Field sites are selected to minimize permitting risk while maximizing scientific return; Great Salt Lake North Arm offers tractable Utah sovereign-lands access and well-characterized communities for ground-truth benchmarking. Backup sites in the Salton Sea and California operator ponds are pre-identified should primary access be delayed. The machine learning platform is designed for extensibility, with the spectra-to-sequence framework structured to accept training data from thermophilic, acidophilic, and alkaliphilic environments in subsequent campaigns, enabling a unified extremophile biogeography model.


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