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Timlin, Jerilyn

Publications and source records attributed to Timlin, Jerilyn.

Hyperspectral Light Sheet Raman Imaging of Leaf Metabolism (Final Report)

This final technical report details the accomplishment and findings of a project that developed technology related to imaging metabolic processes in plants. The report gives technical details of the design, construction and characterization of a Raman microscope system capable of identifying chemical species using the wavelength shifts of scattered excitation light. Some of the unique aspects of the design include: use of a Bessel beam excitation source, which allow long excitation lines that are resistant to scattering in complex media such as plants; excitation at 785 nm to avoid fluorescence emission that can occur in photosynthetic organisms; and a flat optical design that makes construction and alignment significantly simpler. This project also used stable isotope labeling to look at photorespiratory flux in the leaves of three different types of plants that have different photosynthesis pathways. Gas chromatography–mass spectrometry was used to look at which metabolites and amino acids had altered oxygen, carbon and hydrogen uptake under various conditions of environmental oxygen. This generated a rich data set that is being further analyzed to understand metabolic pathways in plants. This project also used the natural fluorescence in sorghum and rice to conduct an extensive experiment across different developmental stages. Spectral differences were identified at most of the developmental stages and these can be attributed to differential pigment and pigment-protein complexes present in different relative abundances as the plant develops.

09 BIOMASS FUELS↗

Algal Predator and Pathogen Signature Verification

The purpose of this PTS was to conduct work with Arizona State University (ASU), specifically to further develop Spectroradiometric-based technology that has potential to function as early warning of the active presence of predators and pathogens in outdoor algal ponds. Chlorella sorokiniana and the pathogen, Vampirovibrio chlorellavorus were selected for investigation because they had previously been implicated in several pond crashes at ASU’s Arizona Center for Algal Technology and Innovation (AzCATI). Sandia conducted small-scale laboratory experiments comparing control and infected cultures of C. sorokiniana . Spectrally-resolved reflectivity data, as well as optical density, and pulse amplitude modulated fluorescence (PAM) were collected and analyzed to identify the spectral response of active V. chlorellavorus infection. The results of this limited, yet robust, experiment confirmed the initial hypothesis that signature V. chlorellavorus infection of C. sorokiniana could be identified based on the presence of a chlorophyll metabolites generated when the algal chlorophyll is degraded by the pathogen.

Timlin, Jerilyn↗