Development of a light-powered microstructure : enhancing thermal actuation with near-infrared absorbent gold nanoparticles.

Development of microscale actuating technologies has considerably added to the toolset for interacting with natural components at the cellular level. Small-scale actuators and switches have potential in areas such as microscale pumping and particle manipulation. Thermal actuation has been used with asymmetric geometry to create large deflections with high force relative to electrostatically driven systems. However, many thermally based techniques require a physical connection for power and operate outside the temperature range conducive for biological studies and medical applications. The work presented here describes the design of an out-of-plane bistable switch that responds to near-infrared light with wavelength-specific response. In contrast to thermal actuating principles that require wired conductive components for Joule heating, the devices shown here are wirelessly powered by near -infrared (IR) light by patterning a wavelength-specific absorbent gold nanoparticle (GNP) film onto the microstructure. An optical window exists which allows near-IR wavelength light to permeate living tissue, and high stress mismatch in the bilayer geometry allows for large actuation at biologically acceptable limits. Patterning the GNP film will allow thermal gradients to be created from a single laser source, and integration of various target wavelengths will allow for microelectromechanical (MEMS) devices with multiple operating modes. An optically induced temperature gradient using wavelength-selective printable or spinnable coatings would provide a versatile method of wireless and non-invasive thermal actuation. This project aims to provide a fundamental understanding of the particle and surface interaction for bioengineering applications based on a “hybrid” of infrared resonant gold nanoparticles and MEMS structures. This hybrid technology has potential applications in light-actuated switches and other mechanical structures. Deposition methods and surface chemistry are integrated with three-dimensional MEMS structures in this work. The long-term goal of this project is a system of light-powered microactuators for exploring cells\u27 response to mechanical stimuli, adding to the fundamental understanding of tissue response to everyday mechanical stresses at the molecular level

Collecting Culture: Explaining Sociability in Collectibles Markets

Cultures, like other group-level phenomena, are the result of a complex and iterative process whereby social environments provide individuals with desires, beliefs, and opportunities that guide individual actions in patterned ways. Actor-Network Theorists have been vocal in their assertion that objects are not passive intermediaries, but rather active mediators of human action. In markets, patterns in the characteristics of the objects for sale make certain trading behaviors more or less effective, profitable, etc. By analyzing books for collectibles that vary in the fungibility of the objects and organization of the markets, I find that the level of market organization and the fungibility of objects for sale are related to differences in the rates of coding the advice provided as `advised sociability,' `sociability traps,' and `anti-sociability.'Master of Art

Exploring connections between pollinator health and human health

Despite recent advances in understanding the role of biodiversity in ecosystem-service provision, the links between the health of ecosystem-service providers and human health remain more uncertain. During the past decade, an increasing number of studies have argued for the positive impacts of healthy pollinator communities (defined as functionally and genetically diverse species assemblages that are sustained over time) on human health. Here, we begin with a systematic review of these impacts, finding only two studies that concomitantly quantified aspects of pollinator health and human health. Next, we identify relevant research relating to four pathways linking pollinator health and human health: Nutrition, medicine provisioning, mental health and environmental quality. These benefits are obtained through improved pollination of nutritious crops and an estimated approximately 28 000 animal-pollinated medicinal plants; the provisioning of pollinator-derived products such as honey; the maintenance of green spaces and biocultural landscapes that improve mental health; and cleaner air, water and food resulting from pollinator-centred initiatives to reduce agrochemical use. We suggest that pollinator diversity could be a proxy for the benefits that landscapes provide to human health. This article is part of the theme issue 'Natural processes influencing pollinator health: From chemistry to landscapes'.Fil: Garibaldi, Lucas Alejandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte. Instituto de Investigaciones en Recursos Naturales, Agroecología y Desarrollo Rural. - Universidad Nacional de Rio Negro. Instituto de Investigaciones en Recursos Naturales, Agroecología y Desarrollo Rural; ArgentinaFil: Gómez Carella, Dulce Sol. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte. Instituto de Investigaciones en Recursos Naturales, Agroecología y Desarrollo Rural. - Universidad Nacional de Rio Negro. Instituto de Investigaciones en Recursos Naturales, Agroecología y Desarrollo Rural; ArgentinaFil: Nabaes Jodar, Diego Nicolás. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte. Instituto de Investigaciones en Recursos Naturales, Agroecología y Desarrollo Rural. - Universidad Nacional de Rio Negro. Instituto de Investigaciones en Recursos Naturales, Agroecología y Desarrollo Rural; ArgentinaFil: Smith, Matthew R.. Harvard University. Harvard School of Public Health; Estados UnidosFil: Timberlake, Thomas P.. University of Bristol; Reino UnidoFil: Myers, Samuel S.. Harvard University. Harvard School of Public Health; Estados Unidos. Harvard University; Estados Unido

Recognizing People by Body Shape Using Deep Networks of Images and Words

Common and important applications of person identification occur at distances and viewpoints in which the face is not visible or is not sufficiently resolved to be useful. We examine body shape as a biometric across distance and viewpoint variation. We propose an approach that combines standard object classification networks with representations based on linguistic (word-based) descriptions of bodies. Algorithms with and without linguistic training were compared on their ability to identify people from body shape in images captured across a large range of distances/views (close-range, 100m, 200m, 270m, 300m, 370m, 400m, 490m, 500m, 600m, and at elevated pitch in images taken by an unmanned aerial vehicle [UAV]). Accuracy, as measured by identity-match ranking and false accept errors in an open-set test, was surprisingly good. For identity-ranking, linguistic models were more accurate for close-range images, whereas non-linguistic models fared better at intermediary distances. Fusion of the linguistic and non-linguistic embeddings improved performance at all, but the farthest distance. Although the non-linguistic model yielded fewer false accepts at all distances, fusion of the linguistic and non-linguistic models decreased false accepts for all, but the UAV images. We conclude that linguistic and non-linguistic representations of body shape can offer complementary identity information for bodies that can improve identification in applications of interest.Comment: 9 pages, 5 figures, 4 table

Whole genome sequencing of Plasmodium falciparum from dried blood spots using selective whole genome amplification

BACKGROUND: Translating genomic technologies into healthcare applications for the malaria parasite Plasmodium falciparum has been limited by the technical and logistical difficulties of obtaining high quality clinical samples from the field. Sampling by dried blood spot (DBS) finger-pricks can be performed safely and efficiently with minimal resource and storage requirements compared with venous blood (VB). Here, the use of selective whole genome amplification (sWGA) to sequence the P. falciparum genome from clinical DBS samples was evaluated, and the results compared with current methods that use leucodepleted VB. METHODS: Parasite DNA with high (>95%) human DNA contamination was selectively amplified by Phi29 polymerase using short oligonucleotide probes of 8-12 mers as primers. These primers were selected on the basis of their differential frequency of binding the desired (P. falciparum DNA) and contaminating (human) genomes. RESULTS: Using sWGA method, clinical samples from 156 malaria patients, including 120 paired samples for head-to-head comparison of DBS and leucodepleted VB were sequenced. Greater than 18-fold enrichment of P. falciparum DNA was achieved from DBS extracts. The parasitaemia threshold to achieve >5× coverage for 50% of the genome was 0.03% (40 parasites per 200 white blood cells). Over 99% SNP concordance between VB and DBS samples was achieved after excluding missing calls. CONCLUSION: The sWGA methods described here provide a reliable and scalable way of generating P. falciparum genome sequence data from DBS samples. The current data indicate that it will be possible to get good quality sequence on most if not all drug resistance loci from the majority of symptomatic malaria patients. This technique overcomes a major limiting factor in P. falciparum genome sequencing from field samples, and paves the way for large-scale epidemiological applications

Endostructural Morphology in Hominoid Mandibular Third Premolars: Geometric Morphometric Analysis of Dentine Crown Shape

In apes, the mandibular third premolar (P3) is adapted for a role in honing the large upper canine. The role of honing was lost early in hominin evolution, releasing the tooth from this functional constraint and allowing it to respond to subsequent changes in masticatory demands. This led to substantial morphological changes, and as such the P3 has featured prominently in systematic analyses of the hominin clade. The application of microtomography has also demonstrated that examination of the enamel-dentine junction (EDJ) increases the taxonomic value of variations in crown morphology. Here we use geometric morphometric techniques to analyze the shape of the P3 EDJ in a broad sample of fossil hominins, modern humans, and extant apes (n = 111). We test the utility of P3 EDJ shape for distinguishing among hominoids, address the affinities of a number of hominin specimens of uncertain taxonomic attribution, and characterize the changes in P3 EDJ morphology across our sample, with particular reference to features relating to canine honing and premolar ‘molarization’. We find that the morphology of the P3 EDJ is useful in taxonomic identification of individual specimens, with a classification accuracy of up to 88%. The P3 EDJ of canine-honing apes displays a tall protoconid, little metaconid development, and an asymmetrical crown shape. Plio-Pleistocene hominin taxa display derived masticatory adaptations at the EDJ, such as the molarized premolars of Australopithecus africanus and Paranthropus, which have well-developed marginal ridges, an enlarged talonid, and a large metaconid. Modern humans and Neanderthals display a tall dentine body and reduced metaconid development, a morphology shared with premolars from Mauer and the Cave of Hearths. Homo naledi displays a P3 EDJ morphology that is unique among our sample; it is quite unlike Middle Pleistocene and recent Homo samples and most closely resembles Australopithecus, Paranthropus and early Homo specimens

Environment Dictates Dependence on Mitochondrial Complex I for NAD+ and Aspartate Production and Determines Cancer Cell Sensitivity to Metformin

Metformin use is associated with reduced cancer mortality, but how metformin impacts cancer outcomes is controversial. Although metformin can act on cells autonomously to inhibit tumor growth, the doses of metformin that inhibit proliferation in tissue culture are much higher than what has been described in vivo. Here, we show that the environment drastically alters sensitivity to metformin and other complex I inhibitors. We find that complex I supports proliferation by regenerating nicotinamide adenine dinucleotide (NAD)+, and metformin's anti-proliferative effect is due to loss of NAD+/NADH homeostasis and inhibition of aspartate biosynthesis. However, complex I is only one of many inputs that determines the cellular NAD+/NADH ratio, and dependency on complex I is dictated by the activity of other pathways that affect NAD+ regeneration and aspartate levels. This suggests that cancer drug sensitivity and resistance are not intrinsic properties of cancer cells, and demonstrates that the environment can dictate sensitivity to therapies that impact cell metabolism. Keywords: cancer metabolism; metformin; biguanide; NAD+/NADH ratio; drug sensitivity; complex I; mitochondria; aspartateNational Institutes of Health (U.S.) (Grant P30CA1405141)National Institutes of Health (U.S.) (Grant GG006413)National Institutes of Health (U.S.) (Grant R01 CA168653)National Institutes of Health (U.S.) (Grant R01 CA201276