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Optical coherence tomography (OCT) leverages light scattering by biological tissues as endogenous contrast to form structural images. Light scattering behavior is dictated by the optical properties of the tissue, which depend on microstructural details at the cellular or sub-cellular level. Methods to measure these properties from OCT intensity data have been explored in the context of a number of biomedical applications seeking to access this sub-resolution tissue microstructure and thereby increase the diagnostic impact of OCT. Most commonly, the optical attenuation coefficient, an analogue of the scattering coefficient, has been used as a surrogate metric linking OCT intensity to subcellular particle characteristics. To record attenuation coefficient data that is accurately representative of the underlying physical properties of a given sample, it is necessary to account for the impact of the OCT imaging system itself on the distribution of light intensity in the sample, including the numerical aperture (NA) of the system and the location of the focal plane with respect to the sample surface, as well as the potential contribution of multiple scattering to the reconstructed intensity signal. Although these considerations complicate attenuation coefficient measurement and interpretation, a suitably calibrated system may potentiate a powerful strategy for gaining additional information about the scattering behavior and microstructure of samples. In this work, we experimentally show that altering the OCT system geometry minimally impacts measured attenuation coefficients in samples presumed to be singly scattering, but changes these measurements in more highly scattering samples. Using both depth-resolved attenuation coefficient data and layer-resolved backscattering coefficients, we demonstrate the retrieval of scattering particle diameter and concentration in tissue-mimicking phantoms, and the impact of presumed multiple scattering on these calculations. We further extend our approach to characterize a murine brain tissue sample and highlight a tumor-bearing region based on increased scattering particle density. Through these methods, we not only enhance conventional OCT attenuation coefficient analysis by decoupling the independent effects of particle size and concentration, but also discriminate areas of strong multiple scattering through minor changes to system topology to provide a framework for assessing the accuracy of these measurements.

 

yEvo is a curriculum for high school students centered around evolution experiments in S. cerevisiae. To adapt the curriculum for remote instruction, we created a new protocol to evolve non-engineered yeast in the presence of caffeine. Evolved strains had increased caffeine tolerance and distinct colony morphologies. Many possessed copy number variations, transposon insertions, and mutations affecting genes with known relationships to caffeine and TOR signaling - which is inhibited by caffeine - and in other genes not previously connected with caffeine. This demonstrates that our accessible, at-home protocol is sufficient to permit novel insights into caffeine tolerance. 

The resources for carrying out and analyzing microbial evolution experiments have become more accessible, making it possible to expand these studies beyond the research laboratory and into the classroom. We developed five connected, standards‐aligned yeast evolution laboratory modules, called “yEvo,” for high school students. The modules enable students to take agency in answering open‐ended research questions. In Module 1, students evolve baker's yeast to tolerate an antifungal drug, and in subsequent modules, investigate how evolved yeasts adapted to this stressful condition at both the phenotype and genotype levels. We used pre‐ and post‐surveys from 72 students at two different schools and post‐interviews with students and teachers to assess our program goals and guide module improvement over 3 years. We measured changes in student conceptions, confidence in scientific practices, and interest in STEM careers. Students who participated in yEvo showed improvements in understanding of activity‐specific concepts and reported increased confidence in designing a valid biology experiment. Student experimental data replicated literature findings and has led to new insights into antifungal resistance. The modules and provided materials, alongside “proof of concept” evaluation metrics, will serve as a model for other university researchers and K − 16 classrooms interested in engaging in open‐ended research questions using yeast as a model system.

 

Determining the optimal treatment course for a dermatologic burn wound requires knowledge of the wound’s severity, as quantified by the depth of thermal damage. In current clinical practice, burn depth is inferred based exclusively on superficial visual assessment, a method which is subject to substantial error rates in the classification of partial thickness (second degree) burns. Here, we present methods for direct, quantitative determination of the depth extent of injury to the dermal collagen matrix using polarization-sensitive optical coherence tomography (PS-OCT). By visualizing the depth-dependence of the degree of polarization of light in the tissue, rather than cumulative retardation, we enable direct and volumetric assessment of local collagen status. We further augment our PS-OCT measurements by visualizing adnexal structures such as hair follicles to relay overall dermal viability in the wounded region. Our methods, which we have validated ex vivo with matched histology, offer an information-rich tool for precise interrogation of burn wound severity and healing potential in both research and clinical settings.

 

The dominant benthic primary producers in coral reef ecosystems are complex holobionts with diverse microbiomes and metabolomes. In this study, we characterize the tissue metabolomes and microbiomes of corals, macroalgae, and crustose coralline algae via an intensive, replicated synoptic survey of a single coral reef system (Waimea Bay, Oʻahu, Hawaii) and use these results to define associations between microbial taxa and metabolites specific to different hosts. Our results quantify and constrain the degree of host specificity of tissue metabolomes and microbiomes at both phylum and genus level. Both microbiome and metabolomes were distinct between calcifiers (corals and CCA) and erect macroalgae. Moreover, our multi-omics investigations highlight common lipid-based immune response pathways across host organisms. In addition, we observed strong covariation among several specific microbial taxa and metabolite classes, suggesting new metabolic roles of symbiosis to further explore.

 

Abstract Scale is a central concept in the geographical sciences and is an intrinsic property of many spatial systems. It also serves as an essential thread in the fabric of many other physical and social sciences, which has contributed to the use of different terminology for similar manifestations of what we refer to as ‘scale’, leading to a surprising amount of diversity around this fundamental concept and its various ‘multiscale’ extensions. To address this, we review common abstractions about spatial scale and how they are employed in quantitative research. We also explore areas where the conceptualizations of multiple spatial scales can be differentiated. This is achieved by first bridging terminology and concepts, and then conducting a scoping review of the topic. A typology for spatial scale is discussed that can be used to categorize its multifarious meanings and measures. This typology is then used to distinguish what we term ‘process scale,’ from other types of spatial scale and to highlight current trends in uncovering aspects of process scale. We end with suggestions on how to further build knowledge regarding spatial processes through the lens of spatial scale.