COLOR PROJECTION SLIDES 35 Mm PHOTOMICROGRAPHS
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Aberrant Colourations in Wild Snakes: Case Study in Neotropical Taxa and a Review of Terminology
SALAMANDRA 57(1): 124–138 Claudio Borteiro et al. SALAMANDRA 15 February 2021 ISSN 0036–3375 German Journal of Herpetology Aberrant colourations in wild snakes: case study in Neotropical taxa and a review of terminology Claudio Borteiro1, Arthur Diesel Abegg2,3, Fabrício Hirouki Oda4, Darío Cardozo5, Francisco Kolenc1, Ignacio Etchandy6, Irasema Bisaiz6, Carlos Prigioni1 & Diego Baldo5 1) Sección Herpetología, Museo Nacional de Historia Natural, Miguelete 1825, Montevideo 11800, Uruguay 2) Instituto Butantan, Laboratório Especial de Coleções Zoológicas, Avenida Vital Brasil, 1500, Butantã, CEP 05503-900 São Paulo, SP, Brazil 3) Universidade de São Paulo, Instituto de Biociências, Departamento de Zoologia, Programa de Pós-Graduação em Zoologia, Travessa 14, Rua do Matão, 321, Cidade Universitária, 05508-090, São Paulo, SP, Brazil 4) Universidade Regional do Cariri, Departamento de Química Biológica, Programa de Pós-graduação em Bioprospecção Molecular, Rua Coronel Antônio Luiz 1161, Pimenta, Crato, Ceará 63105-000, CE, Brazil 5) Laboratorio de Genética Evolutiva, Instituto de Biología Subtropical (CONICET-UNaM), Facultad de Ciencias Exactas Químicas y Naturales, Universidad Nacional de Misiones, Felix de Azara 1552, CP 3300, Posadas, Misiones, Argentina 6) Alternatus Uruguay, Ruta 37, km 1.4, Piriápolis, Uruguay Corresponding author: Claudio Borteiro, e-mail: [email protected] Manuscript received: 2 April 2020 Accepted: 18 August 2020 by Arne Schulze Abstract. The criteria used by previous authors to define colour aberrancies of snakes, particularly albinism, are varied and terms have widely been used ambiguously. The aim of this work was to review genetically based aberrant colour morphs of wild Neotropical snakes and associated terminology. We compiled a total of 115 cases of conspicuous defective expressions of pigmentations in snakes, including melanin (black/brown colour), xanthins (yellow), and erythrins (red), which in- volved 47 species of Aniliidae, Boidae, Colubridae, Elapidae, Leptotyphlopidae, Typhlopidae, and Viperidae. -
Index to the NLM Classification 2011
National Library of Medicine Classification 2011 Index Disease see Tyrosinemias 1-8 5,12-diHETE see Leukotriene B4 1,2-Benzopyrones see Coumarins 5,12-HETE see Leukotriene B4 1,2-Dibromoethane see Ethylene Dibromide 5-HT see Serotonin 1,8-Dihydroxy-9-anthrone see Anthralin 5-HT Antagonists see Serotonin Antagonists 1-Oxacephalosporin see Moxalactam 5-Hydroxytryptamine see Serotonin 1-Propanol 5-Hydroxytryptamine Antagonists see Serotonin Organic chemistry QD 305.A4 Antagonists Pharmacology QV 82 6-Mercaptopurine QV 269 1-Sar-8-Ala Angiotensin II see Saralasin 7S RNA see RNA, Small Nuclear 1-Sarcosine-8-Alanine Angiotensin II see Saralasin 8-Hydroxyquinoline see Oxyquinoline 13-cis-Retinoic Acid see Isotretinoin 8-Methoxypsoralen see Methoxsalen 15th Century History see History, 15th Century 8-Quinolinol see Oxyquinoline 16th Century History see History, 16th Century 17 beta-Estradiol see Estradiol 17-Ketosteroids WK 755 A 17-Oxosteroids see 17-Ketosteroids A Fibers see Nerve Fibers, Myelinated 17th Century History see History, 17th Century Aardvarks see Xenarthra 18th Century History see History, 18th Century Abate see Temefos 19th Century History see History, 19th Century Abattoirs WA 707 2',3'-Cyclic-Nucleotide Phosphodiesterases QU 136 Abbreviations 2,4-D see 2,4-Dichlorophenoxyacetic Acid Chemistry QD 7 2,4-Dichlorophenoxyacetic Acid General P 365-365.5 Organic chemistry QD 341.A2 Library symbols (U.S.) Z 881 2',5'-Oligoadenylate Polymerase see Medical W 13 2',5'-Oligoadenylate Synthetase By specialties (Form number 13 in any NLM -
Raman and Infrared Spectroscopy of Arsenates of the Roselite and Fairfeldite Mineral Subgroups
This may be the author’s version of a work that was submitted/accepted for publication in the following source: Frost, Ray (2009) Raman and infrared spectroscopy of arsenates of the roselite and fair- feldite mineral subgroups. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 71(5), pp. 1788-1794. This file was downloaded from: https://eprints.qut.edu.au/17596/ c Copyright 2009 Elsevier Reproduced in accordance with the copyright policy of the publisher. Notice: Please note that this document may not be the Version of Record (i.e. published version) of the work. Author manuscript versions (as Sub- mitted for peer review or as Accepted for publication after peer review) can be identified by an absence of publisher branding and/or typeset appear- ance. If there is any doubt, please refer to the published source. https://doi.org/10.1016/j.saa.2008.06.039 QUT Digital Repository: http://eprints.qut.edu.au/ Frost, Ray L. (2009) Raman and infrared spectroscopy of arsenates of the roselite and fairfieldite mineral subgroups. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 71(5). pp. 1788-1794. © Copyright 2009 Elsevier Raman and infrared spectroscopy of arsenates of the roselite and fairfieldite mineral subgroups Ray L. Frost• Inorganic Materials Research Program, School of Physical and Chemical Sciences, Queensland University of Technology, GPO Box 2434, Brisbane Queensland 4001, Australia. Abstract Raman spectroscopy complimented with infrared spectroscopy has been used to determine the molecular structure of the roselite arsenate minerals of the roselite and 2+ fairfieldite subgroups of formula Ca2B(AsO4)2.2H2O (where B may be Co, Fe , Mg, 2- Mn, Ni, Zn). -
Powder Denim Sky Teal Midnight Cerulean Navy Turquoise Cornflower Periwinkle Royal Opal Cmg 08458 Cmg 1 26 27 3 4 6 29 30 31 2 32 33
MARCH 2010 House Beautiful sp ring ALL COLO | A BOUT issue BLUE POWDER DENIM SKY TEAL MIDNIGHT CERULEAN NAVY TURQUOISE CORNFLOWER PERIWINKLE ROYAL OPAL CMG 08458 1 26 27 3 4 6 29 30 31 2 32 33 5 28 34 7 8 36 10 11 9 50 BLUE FABRICS 35 14 12 13 15 37 38 41 40 19 39 47 17 43 44 45 18 46 16 20 42 23 24 25 49 21 48 22 50 1 CLOQUE DE COTON 6 ARIPEKA 10 STRIATE IN AQUA. KaTE 14 CHRISSY IN DENIM. ViCTOria 18 FORMIA 22 DJEBEL 26 GASTAAD PLAID IN CaPri. 31 LA GAROUPE 35 LUCE 39 JUPON BOUQUET 43 OcELOT IN AZUL. KaT BURKI 47 KHAN CASHMERE IN COLOR 8. DOMINIQUE KIEffER IN HYdraNGEA. ROGERS GabriEL THROUGH STUdiO HaGAN HOME COLLECTION: IN RUSCELLO. DECORTEX IN GaLET. LELIEVRE THROUGH EriC COHLER FOR LEE JOfa: IN INdiGO. RALPH LaUREN IN NaVY. MadELINE WEINrib IN AZURE BLUE COLLECTION FOR IN BLUE MIX. HOLLAND BY RUBELLI THROUGH & GOffiGON: 203-532-8068. FOUR NYC: 212-475-4414. 212-888-3241. THROUGH BRUNSCHWIG STarK fabriC: 212-355-7186. 800-453-3563. HOME : 888-743-7470. ATELIER: 212-473-3000, X780. AND WarM WHITE. FORTUNY: STarK fabriC: 212-355-7186. & SHErrY: 212-355-6241. BERGAMO: 914-665-0800. & FILS: 914-684-5800. 212-753-7153. 7 MYRSINI 11 SIERRA MADRE 15 TANZANIA IN BLUE. CHarLES 23 CHEVRON BAR 27 VIOLETTA N IN MOONLIGHT. 32 WOOL SATEEN 36 AlTAI IN BLUETTE. 44 HINSON SUEDE 48 BARODA II IN INdiGO ON 2 FIORI IN ATLANTIC ON SEA MIST. -
Bougainvillea Greenthread Madagascar Periwinkle Desert Willow
TOP TEN PLANTS FOR A DESERT ISLAND Page 1 of 1 American Beautyberry Purple Trailing Lantana Callicarpa americana Lantana montevidensis 'Purple' from article in Rockport Pilot by from Dr. Michael Womack: This Ernie Edmundson: Early spring is tough plant not only blossoms most the time to cut them down before of the year, but it is also drought and they put on their new spring growth. sun hardy. The most effective use They can be trimmed back almost to of these plants is often mass the ground, however unpruned plantings in sunny areas with well- plants will develop a weeping effect drained soils. [The smaller the leaf, . with purple, or in some cases, the smaller the plant will be]. The white berries in the fall. shortest varieties of lantana commonly are called trailing lantana. Bougainvillea Madagascar Periwinkle Bougainvillea sp. Catharanthus roseus Hummingbirds are attracted to from www.wikipedia.com: It is noted bougainvillea but cannot use it for for its long flowering period, an energy source. Be careful throughout the year in tropical around play areas because of the conditions, and from spring to late thorns. Great vine for large autumn in warm temperate climates. containers to decorate hot patios Tolerates wind, bushy, thrives in and plazas. It can be trained as a humid heat. The alkaloids shrub or clipped into shapes. vincristine and vinblastine from its sap have been shown to be an effective treatment for leukaemia. Esperanza Turk's Cap Drummondii Tecoma stans Malvaviscus arboreus 'Drummondii' LARVAL HOST for: Plebeian Primary food source for migrating sphinx moth (Paratrea plebeja). -
2003Session3.Pdf
THE SITUATION OF GRAPEVINE YELLOWS AND CURRENT RESEARCH DIRECTIONS: DISTRIBUTION, DIVERSITY, VECTORS, DIFFUSION AND CONTROL E. Boudon-Padieu Biologie et écologie des phytoplasmes, UMR 1088 Plante Microbe Environnement, INRA – Université de Bourgogne, Domaine d’Epoisses, BP 86510 – 21065 Dijon Cedex France Grapevine yellows (GY) are known now for 50 years. After the first appearance of Flavescence dorée (FD) in West-South France in the 1950’s, similar diseases have been observed in vineyards of other regions or countries (22) in Europe, North-America, Asia Minor and Australia. Typical symptoms are leaf rolling and discoloration of veins and laminae, uneven or total lack of lignification of canes, flower abortion or berry withering. Eventually, severe decline and death occur with sensitive varieties or with particular GY diseases. All these diseases have been associated with phytoplasmas. Phytoplasmas, discovered in 1967, are wall-less intracellular bacterias restricted to phloem sieve tubes and transmitted only by vector insects in which they multiply and circulate. Recently, comparisons of conserved regions in their genomic DNA, have permitted to classify all known phytoplasmas into about 20 groups and subgroups within a monophyletic clade in the Class Mollicutes, closest to the Acholeplasma clade (57, 78). Numerous DNA probes have been designed that permit diagnosis and identification of phytoplasmas in plant tissues and in insects. This, together with transmission assays, has also permitted the recent identification of new phytoplasma vectors. Though Koch’s postulate cannot be fully satisfied with non-culturable pathogen agents, it is now considered that phytoplasmas are responsible for typical GY symptoms. These conclusions have been reached because of transmission experiments with natural vectors in the case of Flavescence dorée (FD) and Bois noir (BN), of the similarity of symptoms caused world wide by GY diseases on numerous grapevine cultivars and of consistent detection of phytoplasmas in affected grapevines and in infective insect vectors. -
Linking Melanism to Brain Development: Expression of a Melanism-Related Gene in Barn Owl Feather Follicles Covaries with Sleep O
Scriba et al. Frontiers in Zoology 2013, 10:42 http://www.frontiersinzoology.com/content/10/1/42 RESEARCH Open Access Linking melanism to brain development: expression of a melanism-related gene in barn owl feather follicles covaries with sleep ontogeny Madeleine F Scriba1,2†, Anne-Lyse Ducrest2†, Isabelle Henry2, Alexei L Vyssotski3, Niels C Rattenborg1*† and Alexandre Roulin2*† Abstract Background: Intra-specific variation in melanocyte pigmentation, common in the animal kingdom, has caught the eye of naturalists and biologists for centuries. In vertebrates, dark, eumelanin pigmentation is often genetically determined and associated with various behavioral and physiological traits, suggesting that the genes involved in melanism have far reaching pleiotropic effects. The mechanisms linking these traits remain poorly understood, and the potential involvement of developmental processes occurring in the brain early in life has not been investigated. We examined the ontogeny of rapid eye movement (REM) sleep, a state involved in brain development, in a wild population of barn owls (Tyto alba) exhibiting inter-individual variation in melanism and covarying traits. In addition to sleep, we measured melanistic feather spots and the expression of a gene in the feather follicles implicated in melanism (PCSK2). Results: As in mammals, REM sleep declined with age across a period of brain development in owlets. In addition, inter-individual variation in REM sleep around this developmental trajectory was predicted by variation in PCSK2 expression in the feather follicles, with individuals expressing higher levels exhibiting a more precocial pattern characterized by less REM sleep. Finally, PCSK2 expression was positively correlated with feather spotting. Conclusions: We demonstrate that the pace of brain development, as reflected in age-related changes in REM sleep, covaries with the peripheral activation of the melanocortin system. -
Color Chart Colorchart
Color Chart AMERICANA ACRYLICS Snow (Titanium) White White Wash Cool White Warm White Light Buttermilk Buttermilk Oyster Beige Antique White Desert Sand Bleached Sand Eggshell Pink Chiffon Baby Blush Cotton Candy Electric Pink Poodleskirt Pink Baby Pink Petal Pink Bubblegum Pink Carousel Pink Royal Fuchsia Wild Berry Peony Pink Boysenberry Pink Dragon Fruit Joyful Pink Razzle Berry Berry Cobbler French Mauve Vintage Pink Terra Coral Blush Pink Coral Scarlet Watermelon Slice Cadmium Red Red Alert Cinnamon Drop True Red Calico Red Cherry Red Tuscan Red Berry Red Santa Red Brilliant Red Primary Red Country Red Tomato Red Naphthol Red Oxblood Burgundy Wine Heritage Brick Alizarin Crimson Deep Burgundy Napa Red Rookwood Red Antique Maroon Mulberry Cranberry Wine Natural Buff Sugared Peach White Peach Warm Beige Coral Cloud Cactus Flower Melon Coral Blush Bright Salmon Peaches 'n Cream Coral Shell Tangerine Bright Orange Jack-O'-Lantern Orange Spiced Pumpkin Tangelo Orange Orange Flame Canyon Orange Warm Sunset Cadmium Orange Dried Clay Persimmon Burnt Orange Georgia Clay Banana Cream Sand Pineapple Sunny Day Lemon Yellow Summer Squash Bright Yellow Cadmium Yellow Yellow Light Golden Yellow Primary Yellow Saffron Yellow Moon Yellow Marigold Golden Straw Yellow Ochre Camel True Ochre Antique Gold Antique Gold Deep Citron Green Margarita Chartreuse Yellow Olive Green Yellow Green Matcha Green Wasabi Green Celery Shoot Antique Green Light Sage Light Lime Pistachio Mint Irish Moss Sweet Mint Sage Mint Mint Julep Green Jadeite Glass Green Tree Jade -
Title How Common Is Albinism Really? Colour Aberrations in Indian Birds Reviewed
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Natural History Museum Repository Title How common is albinism really? Colour aberrations in Indian birds reviewed Authors Van Grouw, H; Mahabal, A; Sharma, RM; Thakur, S Description The file attached is the Published/publisher’s pdf version of the article. How common is albinism really? Colour aberrations in Indian birds reviewed Anil Mahabal, Hein van Grouw, Radheshyam Murlidhar Sharma & Sanjay Thakur eople have always been intrigued by aberrant cluding galliforms Galliformes, nightjars Capri Ply coloured birds, and therefore sightings of mulgidae, bustards Otididae, owls Strigidae and these individuals are often reported in the litera turacos Musophagidae. ture. Contrary to popular belief, birds with a col Melanins can be divided into two forms; eu our aberration do not necessarily fall victim to melanin and phaeomelanin. Depending on con natural predators and often survive for a long time centration and distribution within the feather, (van Grouw 2012). This also increases their chance eumelanin is responsible for black, grey and/or of being seen and recorded by birders. dark brown colours. Phaeomelanin is responsible In general, plumage colour is the result of bio for warm, reddishbrown to pale buff colours, de logical pigments (biochromes), structural colour pending on concentration and distribution. Both (selective light reflection due to the structure of melanins together can give a wide range of grey the feather), or a combination of the two. The two ishbrown colours. In skin and eyes, only eu most common pigments that determine plumage melanin is present (Lubnow 1963, van Grouw colour in birds are melanins and carotenoids (Fox 2006, 2013). -
Clarke Jeff a 201709 Mscproj
THE CHARACTERIZATION OF ARSENIC MINERAL PHASES FROM LEGACY MINE WASTE AND SOIL NEAR COBALT, ONTARIO by Jeff Clarke A research project submitted to the Department of Geological Sciences and Geological Engineering In conformity with the requirements for the degree of Master of Science in Applied Geology Queen’s University Kingston, Ontario, Canada (July, 2017) Copyright © Jeff Clarke, 2017 i ABSTRACT The Cobalt-Coleman silver (Ag) mining camp has a long history of mining dating back to 1903. Silver mineralization is hosted within carbonate veins and occurs in association with Fe-Co-Ni arsenide and sulpharsenide mineral species. The complex mineralogy presented challenges to early mineral processing methods with varying success of Ag recovery and a significant amount of arsenic (As) in waste material which was disposed in the numerous tailings deposits scattered throughout the mining camp, and in many instances disposed of uncontained. The oxidation and dissolution of As-bearing mineral phases in these tailings and legacy waste sites releases As into the local aquatic environment. Determining the distribution of primary and secondary As mineral species in different legacy mine waste materials provides an understanding of the stability of As. Few studies have included detailed advanced mineralogical characterization of As mineral species from legacy mine waste in the Cobalt area. As part of this study, a total of 28 samples were collected from tailings, processed material near mill sites and soils from the legacy Nipissing and Cart Lake mining sites. The samples were analyzed for bulk chemistry to delineate material with strongly elevated As returned from all sample sites. This sampling returned highly elevated As with up to 6.01% As from samples near mill sites, 1.71% As from tailings and 0.10% As from soils. -
Endogenous Retrovirus Insertion in the KIT Oncogene Determines White and White Spotting in Domestic Cats Victor A
Nova Southeastern University NSUWorks Biology Faculty Articles Department of Biological Sciences 9-1-2014 Endogenous Retrovirus Insertion in the KIT Oncogene Determines White and White spotting in Domestic Cats Victor A. David National Cancer Institute at Frederick Marilyn Menotti-Raymond National Cancer Institute at Frederick Andrea Coots Wallace National Cancer Institute at Frederick Melody E. Roelke National Cancer Institute at Frederick; Bethesda Leidos Biomedical Research James Kehler National Institute of Diabetes and Digestive and Kidney Diseases See next page for additional authors Follow this and additional works at: https://nsuworks.nova.edu/cnso_bio_facarticles Part of the Genetics and Genomics Commons NSUWorks Citation David, Victor A.; Marilyn Menotti-Raymond; Andrea Coots Wallace; Melody E. Roelke; James Kehler; Robert Leighty; Eduardo Eizirik; Steven S. Hannah; George Nelson; Alejandro A. Schaffer; Catherine J. Connelly; Stephen J. O'Brien; and David K. Ryugo. 2014. "Endogenous Retrovirus Insertion in the KIT Oncogene Determines White and White spotting in Domestic Cats." G3 4, (10): 1881-1891. https://nsuworks.nova.edu/cnso_bio_facarticles/741 This Article is brought to you for free and open access by the Department of Biological Sciences at NSUWorks. It has been accepted for inclusion in Biology Faculty Articles by an authorized administrator of NSUWorks. For more information, please contact [email protected]. Authors Victor A. David, Marilyn Menotti-Raymond, Andrea Coots Wallace, Melody E. Roelke, James Kehler, Robert Leighty, Eduardo Eizirik, Steven S. Hannah, George Nelson, Alejandro A. Schaffer, Catherine J. Connelly, Stephen J. O'Brien, and David K. Ryugo This article is available at NSUWorks: https://nsuworks.nova.edu/cnso_bio_facarticles/741 INVESTIGATION Endogenous Retrovirus Insertion in the KIT Oncogene Determines White and White spotting in Domestic Cats Victor A. -
CLASSIC RAYON 100% Viscose
CLASSIC RAYON 100% viscose While every attempt is made to reproduce thread colors accurately, colors on your monitor or print out may not precisely match thread colors. Color names are for your reference only. When ordering please refer to each color by color number. 1013 Peach Blush 1111 Evening Mist 1015 Desert Bloom 1031 Frosted Lavender 1317 Blush Pink 1235 Crocus 1220 Conch Shell 1320 Purple Heart 1307 Raspberry Punch 1388 Plum 1485 Electric Red 1319 Iris 1039 Brick Red 1488 Dark Magenta 1038 Barn Red 1310 Magenta 1114 Pink Petal 1321 Bubble Gum Pink 1115 Powder Puff 1121 Candy Heart 1315 Pink Grapefruit 1309 Dahlia 1148 Rustic Pink 1109 Pink Rose 1384 Merlot 1110 Fuchsia 1385 Garnet 1383 Pink Pansy 1182 Mulberry 1187 Orchid 1281 Radish 1234 Hibiscus 1184 Scarlet Rose 1117 Flamingo Pink 1154 Lipstick Rose 1183 Cranberry 1107 Honeysuckle 1389 Bordeaux 1014 Bermuda Sand 1034 Vintage Rose 1120 Baby Pink 1119 English Rose 1116 Cotton Candy 1035 Burgundy 1108 Pink Carnation 1386 Eggplant 1354 Watermelon 1356 Pink Pearl 1081 Azalea 1141 Mauve 1186 Ruby Slipper 1382 Colonial Rose 1381 Ripe Raspberry 1236 Plum Brandy 3 4 CLASSIC RAYON 100% viscose While every attempt is made to reproduce thread colors accurately, colors on your monitor or print out may not precisely match thread colors. Color names are for your reference only. When ordering please refer to each color by color number. 1261 Lavendula 1198 Moonstone 1266 Regal Blue 1030 Light Periwinkle 1166 Hanukkah Blue 1364 Storm Sky Blue 1466 Sailor Blue 1365 Dusty Plum 1335 Dark Periwinkle