A hybrid hair model using three dimensional fuzzy textures

Cataloged from PDF version of article.Human hair modeling and rendering have always been a challenging topic in computer graphics. The techniques for human hair modeling consist of explicit geometric models as well as volume density models. Recently, hybrid cluster models have also been successful in this subject. In this study, we present a novel three dimensional texture model called 3D Fuzzy Textures and algorithms to generate them. Then, we use the developed model along with a cluster model to give human hair complex hairstyles such as curly and wavy styles. Our model requires little user effort to model curly and wavy hair styles. With this study, we aim at eliminating the drawbacks of the volume density model and the cluster hair model with 3D fuzzy textures. A three dimensional cylindrical texture mapping function is introduced for mapping purposes. Current generation graphics hardware is utilized in the design of rendering system enabling high performance rendering.Aran, Medeni ErolM.S

Spatially Explicit Population Estimates of the Florida Black Bear

The Florida black bear (Ursus americanus floridanus) is currently comprised of 7 isolated subpopulations: Apalachicola, Eglin, Osceola, Ocala/St. Johns, Chassahowitzka, Highlands/Glades, and Big Cypress. The last statewide assessment of Florida black bear population dynamics was conducted by Simek et al. (2005) using traditional capture-markrecapture methods. The subspecies was removed from Florida’s List of State Threatened Species in 2012 contingent upon the formulation of a management plan that would maintain viable subpopulations of black bears in suitable habitat. Accurate population estimates for each of the remaining black bear subpopulations in Florida were needed to achieve the management goals of this plan. I used spatially explicit capture-recapture (SCR) within a maximum likelihood inference framework to estimate population density (D) and abundance (N) for the Osceola, Ocala/St. Johns, Eglin, Apalachicola, and Big Cypress subpopulations; these 5 subpopulations constitute the bulk of the statewide population. I constructed genetic capture histories for each subpopulation from genotyped hair samples taken from barbed-wire sampling stations (henceforth referred to in this document as hair snares). I used a 3 × 3 hair snare cluster layout with 2 km between hair snares and 16 km between cluster centers. I created covariates of density from land use/land cover (LULC) data to model heterogeneity in density across study areas. Model-averaged population estimates were 120.3 bears (95% CI = 61.1 – 269.1) or 0.025 bears/km2 [bears per square kilometer] (95% CI = 0.013 – 0.056) for the Eglin subpopulation, 1,060.3 bears (95% CI = 825.4 – 1,385.9) or 0.082 bears/km2 (95% CI = 0.064 – 0.107) for Apalachicola, 492.9 bears (95 % CI = 319.5 – 792.4) or 0.127 bears/km2 (95% CI = 0.082 – 0.203) for Osceola, 1,192.6 bears (95% CI = 950.8 – 1,519.5) or 0.127 bears/km2 (95% CI =0.101 – 0.161) for Ocala/St. Johns, and 1,037.4 bears (95% CI = 756.1 – 1,444.6) or 0.131 bears/km2 (95% CI = 0.096 – 0.183) for Big Cypress. Effects of covariates on density estimates varied among study areas. The total population estimate was 3,908.8 bears (95% CI = 2,916.2 – 5,425.8). The cluster sampling method allowed abundance to be estimated across extensive areas that would not have been possible otherwise

Hair cluster detection model based on dermoscopic images

Introduction: Hair loss has always bothered many people, with numerous individuals potentially facing the issue of sparse hair.Methods: Due to a scarcity of accurate research on detecting sparse hair, this paper proposes a sparse hair cluster detection model based on improved object detection neural network and medical images of sparse hair under dermatoscope to optimize the evaluation of treatment outcomes for hair loss patients. A new Multi-Level Feature Fusion Module is designed to extract and fuse features at different levels. Additionally, a new Channel-Space Dual Attention Module is proposed to consider both channel and spatial dimensions simultaneously, thereby further enhancing the model’s representational capacity and the precision of sparse hair cluster detection.Results: After testing on self-annotated data, the proposed method is proven capable of accurately identifying and counting sparse hair clusters, surpassing existing methods in terms of accuracy and efficiency.Discussion: Therefore, it can work as an effective tool for early detection and treatment of sparse hair, and offer greater convenience for medical professionals in diagnosis and treatment

A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle

Genodermatoses, such as heritable skin disorders, mostly represent Mendelian conditions. Congenital hypotrichosis (HY) characterize a condition of being born with less hair than normal. The purpose of this study was to characterize the clinicopathological phenotype of a breed-specific non-syndromic form of HY in Hereford cattle and to identify the causative genetic variant for this recessive disorder. Affected calves showed a very short, fine, wooly, kinky and curly coat over all parts of the body, with a major expression in the ears, the inner part of the limbs, and in the thoracic-abdominal region. Histopathology showed a severely altered morphology of the inner root sheath (IRS) of the hair follicle with abnormal Huxley and Henle’s layers and severely dysplastic hair shafts. A genome-wide association study revealed an association signal on chromosome 5. Homozygosity mapping in a subset of cases refined the HY locus to a 690 kb critical interval encompassing a cluster of type II keratin encoding genes. Protein-coding exons of six positional candidate genes with known hair or hair follicle function were re-sequenced. This revealed a protein-changing variant in the KRT71 gene that encodes a type II keratin specifically expressed in the IRS of the hair follicle (c.281delTGTGCCCA; p.Met94AsnfsX14). Besides obvious phenocopies, a perfect concordance between the presence of this most likely pathogenic loss-of-function variant located in the head domain of KRT71 and the HY phenotype was found. This recessive KRT71-related form of hypotrichosis provides a novel large animal model for similar human conditions. The results have been incorporated in the Online Mendelian Inheritance in Animals (OMIA) database (OMIA 002114-9913)

Learning Face Age Progression: A Pyramid Architecture of GANs

The two underlying requirements of face age progression, i.e. aging accuracy and identity permanence, are not well studied in the literature. In this paper, we present a novel generative adversarial network based approach. It separately models the constraints for the intrinsic subject-specific characteristics and the age-specific facial changes with respect to the elapsed time, ensuring that the generated faces present desired aging effects while simultaneously keeping personalized properties stable. Further, to generate more lifelike facial details, high-level age-specific features conveyed by the synthesized face are estimated by a pyramidal adversarial discriminator at multiple scales, which simulates the aging effects in a finer manner. The proposed method is applicable to diverse face samples in the presence of variations in pose, expression, makeup, etc., and remarkably vivid aging effects are achieved. Both visual fidelity and quantitative evaluations show that the approach advances the state-of-the-art.Comment: CVPR 2018. V4 and V2 are the same, i.e. the conference version; V3 is a related but different work, which is mistakenly submitted and will be submitted as a new arXiv pape

Shedding light on melanins within in situ human eye melanocytes using 2-photon microscopy profiling techniques.

Choroidal melanocytes (HCMs) are melanin-producing cells in the vascular uvea of the human eye (iris, ciliary body and choroid). These cranial neural crest-derived cells migrate to populate a mesodermal microenvironment, and display cellular functions and extracellular interactions that are biologically distinct to skin melanocytes. HCMs (and melanins) are important in normal human eye physiology with roles including photoprotection, regulation of oxidative damage and immune responses. To extend knowledge of cytoplasmic melanins and melanosomes in label-free HCMs, a non-invasive 'fit-free' approach, combining 2-photon excitation fluorescence lifetimes and emission spectral imaging with phasor plot segmentation was applied. Intracellular melanin-mapped FLIM phasors showed a linear distribution indicating that HCM melanins are a ratio of two fluorophores, eumelanin and pheomelanin. A quantitative histogram of HCM melanins was generated by identifying the image pixel fraction contributed by phasor clusters mapped to varying eumelanin/pheomelanin ratio. Eumelanin-enriched dark HCM regions mapped to phasors with shorter lifetimes and longer spectral emission (580-625 nm) and pheomelanin-enriched lighter pigmented HCM regions mapped to phasors with longer lifetimes and shorter spectral emission (550-585 nm). Overall, we demonstrated that these methods can identify and quantitatively profile the heterogeneous eumelanins/pheomelanins within in situ HCMs, and visualize melanosome spatial distributions, not previously reported for these cells

A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats.

One of the salient features of the domestic cat is the aesthetics of its fur. The Selkirk Rex breed is defined by an autosomal dominant woolly rexoid hair (ADWH) abnormality that is characterized by tightly curled hair shafts. A genome-wide case - control association study was conducted using 9 curly coated Selkirk Rex and 29 controls, including straight-coated Selkirk Rex, British Shorthair and Persian, to localize the Selkirk autosomal dominant rexoid locus (SADRE). Although the control cats were from different breed lineages, they share recent breeding histories and were validated as controls by Bayesian clustering, multi-dimensional scaling and genomic inflation. A significant association was found on cat chromosome B4 (Praw = 2.87 × 10(-11)), and a unique haplotype spanning ~600 Kb was found in all the curly coated cats. Direct sequencing of four candidate genes revealed a splice site variant within the KRT71 gene associated with the hair abnormality in Selkirk Rex