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Geographic and Individual Variation in Carotenoid Coloration in Golden-Crowned Kinglets (Regulus Satrapa)
University of Windsor Scholarship at UWindsor Electronic Theses and Dissertations Theses, Dissertations, and Major Papers 2009 Geographic and individual variation in carotenoid coloration in golden-crowned kinglets (Regulus satrapa) Celia Chui University of Windsor Follow this and additional works at: https://scholar.uwindsor.ca/etd Recommended Citation Chui, Celia, "Geographic and individual variation in carotenoid coloration in golden-crowned kinglets (Regulus satrapa)" (2009). Electronic Theses and Dissertations. 280. https://scholar.uwindsor.ca/etd/280 This online database contains the full-text of PhD dissertations and Masters’ theses of University of Windsor students from 1954 forward. These documents are made available for personal study and research purposes only, in accordance with the Canadian Copyright Act and the Creative Commons license—CC BY-NC-ND (Attribution, Non-Commercial, No Derivative Works). Under this license, works must always be attributed to the copyright holder (original author), cannot be used for any commercial purposes, and may not be altered. Any other use would require the permission of the copyright holder. Students may inquire about withdrawing their dissertation and/or thesis from this database. For additional inquiries, please contact the repository administrator via email ([email protected]) or by telephone at 519-253-3000ext. 3208. GEOGRAPHIC AND INDIVIDUAL VARIATION IN CAROTENOID COLORATION IN GOLDEN-CROWNED KINGLETS ( REGULUS SATRAPA ) by Celia Kwok See Chui A Thesis Submitted to the Faculty of Graduate Studies through Biological Sciences in Partial Fulfillment of the Requirements for the Degree of Master of Science at the University of Windsor Windsor, Ontario, Canada 2009 © 2009 Celia Kwok See Chui Geographic and individual variation in carotenoid coloration in golden-crowned kinglets (Regulus satrapa ) by Celia Kwok See Chui APPROVED BY: ______________________________________________ Dr. -
Mimicry and Defense
3/24/2015 Professor Donald McFarlane Mimicry and Defense Protective Strategies Camouflage (“Cryptic coloration”) Diverse Coloration Diversion Structures Startle Structures 2 1 3/24/2015 Camouflage (“Cryptic coloration”) Minimize 3d shape, e.g. flatfish Halibut (Hippoglossus hippoglossus) 3 4 2 3/24/2015 Counter‐Shading 5 Disruptive Coloration 6 3 3/24/2015 Polymorphism – Cepeae snails 7 Polymorphism – Oophaga granuliferus 8 4 3/24/2015 Polymorphism – 9 Polymorphism – Oophaga Geographic locations of study populations and their color patterns. (A) Map of the pacific coast of Colombia showing the three study localities: in blue Oophaga histrionica, in orange O. lehmanni, and in green the pHYB population. (B) Examples of color patterns of individuals from the pHYB population (1–4) and the pattern from a hybrid between Oophaga histrionica and O. lehmanni bred in the laboratory (H) 10 5 3/24/2015 Diversion Structures 11 Startle Structures 12 6 3/24/2015 Warning Coloration (Aposematic coloration) Advertise organism as distasteful, toxic or venomous Problem: Predators must learn by attacking prey; predator learning is costly to prey. Therefore strong selective pressure to STANDARDIZE on a few colors/patterns. This is MULLERIAN MIMICRY. Most common is yellow/black, or red/yellow/black 13 Warning Coloration (Aposematic coloration) Bumblebee (Bombus Black and yellow mangrove snake (Boiga sp.) Sand Wasp (bembix oculata) dendrophila) Yellow‐banded poison dart frog (Dendrobates leucomelas Fire salamander ( Salamandra salamandra) 14 7 3/24/2015 Warning Coloration (Aposematic coloration) coral snakes (Micrurus sp.) ~ 50 species in two families, all venomous 15 Batesian Mimicry 1862 –Henry Walter Bates; “A Naturalist on the River Amazons” 16 8 3/24/2015 Batesian Mimicry Batesian mimics “cheat” –they lack toxins, venom, etc. -
Mimicry - Ecology - Oxford Bibliographies 12/13/12 7:29 PM
Mimicry - Ecology - Oxford Bibliographies 12/13/12 7:29 PM Mimicry David W. Kikuchi, David W. Pfennig Introduction Among nature’s most exquisite adaptations are examples in which natural selection has favored a species (the mimic) to resemble a second, often unrelated species (the model) because it confuses a third species (the receiver). For example, the individual members of a nontoxic species that happen to resemble a toxic species may dupe any predators by behaving as if they are also dangerous and should therefore be avoided. In this way, adaptive resemblances can evolve via natural selection. When this phenomenon—dubbed “mimicry”—was first outlined by Henry Walter Bates in the middle of the 19th century, its intuitive appeal was so great that Charles Darwin immediately seized upon it as one of the finest examples of evolution by means of natural selection. Even today, mimicry is often used as a prime example in textbooks and in the popular press as a superlative example of natural selection’s efficacy. Moreover, mimicry remains an active area of research, and studies of mimicry have helped illuminate such diverse topics as how novel, complex traits arise; how new species form; and how animals make complex decisions. General Overviews Since Henry Walter Bates first published his theories of mimicry in 1862 (see Bates 1862, cited under Historical Background), there have been periodic reviews of our knowledge in the subject area. Cott 1940 was mainly concerned with animal coloration. Subsequent reviews, such as Edmunds 1974 and Ruxton, et al. 2004, have focused on types of mimicry associated with defense from predators. -
Coral Reefs Biology 200 Lecture Notes and Study Guide David A
Coral Reefs Biology 200 Lecture Notes and Study Guide David A. Krupp Fall 2001 © Copyright 1 Using this Lecture Outline and Study Guide This lecture outline and study guide was developed to assist you in your studies for this class. It was not meant to replace your attendance and active participation in class, including taking your own lecture notes, nor to substitute for reading and understanding text assignments. In addition, the information presented in this outline and guide does not necessarily represent all of the information that you are expected to learn and understand in this course. You should try to integrate the information presented here with that presented in lecture and in other written materials provided. It is highly recommended that you fully understand the vocabulary and study questions presented. The science of biology is always changing. New information and theories are always being presented, replacing outdated information and theories. In addition, there may be a few errors (content, spelling, and typographical) in this first edition. Thus, this outline and guide may be subject to revision and corrections during the course of the semester. These changes will be announced during class time. Note that this lecture outline and study guide may not be copied nor reproduced in any form without the permission of the author. TABLE OF CONTENTS The Nature of Natural Science ........................................................ 1 The Characteristics of Living Things ............................................... 6 The -
Defensive Behaviors of Deep-Sea Squids: Ink Release, Body Patterning, and Arm Autotomy
Defensive Behaviors of Deep-sea Squids: Ink Release, Body Patterning, and Arm Autotomy by Stephanie Lynn Bush A dissertation submitted in partial satisfaction of the requirements for the degree of Doctor of Philosophy in Integrative Biology in the Graduate Division of the University of California, Berkeley Committee in Charge: Professor Roy L. Caldwell, Chair Professor David R. Lindberg Professor George K. Roderick Dr. Bruce H. Robison Fall, 2009 Defensive Behaviors of Deep-sea Squids: Ink Release, Body Patterning, and Arm Autotomy © 2009 by Stephanie Lynn Bush ABSTRACT Defensive Behaviors of Deep-sea Squids: Ink Release, Body Patterning, and Arm Autotomy by Stephanie Lynn Bush Doctor of Philosophy in Integrative Biology University of California, Berkeley Professor Roy L. Caldwell, Chair The deep sea is the largest habitat on Earth and holds the majority of its’ animal biomass. Due to the limitations of observing, capturing and studying these diverse and numerous organisms, little is known about them. The majority of deep-sea species are known only from net-caught specimens, therefore behavioral ecology and functional morphology were assumed. The advent of human operated vehicles (HOVs) and remotely operated vehicles (ROVs) have allowed scientists to make one-of-a-kind observations and test hypotheses about deep-sea organismal biology. Cephalopods are large, soft-bodied molluscs whose defenses center on crypsis. Individuals can rapidly change coloration (for background matching, mimicry, and disruptive coloration), skin texture, body postures, locomotion, and release ink to avoid recognition as prey or escape when camouflage fails. Squids, octopuses, and cuttlefishes rely on these visual defenses in shallow-water environments, but deep-sea cephalopods were thought to perform only a limited number of these behaviors because of their extremely low light surroundings. -
Experiential Training in Florida and the Florida Keys. a Pretrip Training Manual
DOCUMENT RESUME ED 341 547 SE 052 352 AUTHOR Baker, Claude D., Comp.; And Others TITLE Experiential Training in Florida and the Florida Keys. A Pretrip Training Manual. PUB DATE May 91 NOTE 82p.; For field trip guidelines, see ED 327 394. PUB TYPE Guides - Non-Classroom Use (055) -- Guides - Classroom Use - Teaching Guides (For Teacher)(052) EDRS PRICE MF01/PC04 Plus Postage. DESCRIPTORS Animals; Classification; *Ecology; Environmental Education; Estuaries; *Field Trips; Higher Educatioa; Ichthyology; *Marine Biology; Plant Identification; Plants (Botany); *Resource Materials; Science Activities; Science Education; Secondary Education IDENTIFIERS Coral Reefs; Dichotomous Keys; *Florida ABSTRACT This document is a pretrip instruction manual that can be used by secondary school and college teachers who are planning trips to visit the tropical habitats in South Florida. The material is divided into two parts:(1) several fact sheets on the various habitats in South Florida; and (2) a number of species lists for various areas. Factsheets on the classification of marine environments, the zones of the seashore, estuaries, mangroves, seagrass meadows, salt marshes, and coral reefs are included. The species lists included algae, higher plants, sponges, worms, mollusks, bryozoans, arthropods, echinoderms, vertebrates,I insects, and other invertebrates. The scientific name, common name, and a brief description are supplied for all species. Activities on the behavior and social life of fish, a dichotomous key for seashells, and a section that lists -
Factors Affecting Counterillumination As a Cryptic Strategy
Reference: Biol. Bull. 207: 1–16. (August 2004) © 2004 Marine Biological Laboratory Propagation and Perception of Bioluminescence: Factors Affecting Counterillumination as a Cryptic Strategy SO¨ NKE JOHNSEN1,*, EDITH A. WIDDER2, AND CURTIS D. MOBLEY3 1Biology Department, Duke University, Durham, North Carolina 27708; 2Marine Science Division, Harbor Branch Oceanographic Institution, Ft. Pierce, Florida 34946; and 3Sequoia Scientific Inc., Bellevue, Washington 98005 Abstract. Many deep-sea species, particularly crusta- was partially offset by the higher contrast attenuation at ceans, cephalopods, and fish, use photophores to illuminate shallow depths, which reduced the sighting distance of their ventral surfaces and thus disguise their silhouettes mismatches. This research has implications for the study of from predators viewing them from below. This strategy has spatial resolution, contrast sensitivity, and color discrimina- several potential limitations, two of which are examined tion in deep-sea visual systems. here. First, a predator with acute vision may be able to detect the individual photophores on the ventral surface. Introduction Second, a predator may be able to detect any mismatch between the spectrum of the bioluminescence and that of the Counterillumination is a common form of crypsis in the background light. The first limitation was examined by open ocean (Latz, 1995; Harper and Case, 1999; Widder, modeling the perceived images of the counterillumination 1999). Its prevalence is due to the fact that, because the of the squid Abralia veranyi and the myctophid fish Cera- downwelling light is orders of magnitude brighter than the toscopelus maderensis as a function of the distance and upwelling light, even an animal with white ventral colora- visual acuity of the viewer. -
Deceptive Coloration - Natureworks 01/04/20, 11:58 AM
Deceptive Coloration - NatureWorks 01/04/20, 11:58 AM Deceptive Coloration Deceptive coloration is when an organism's color Mimicry fools either its predators or its prey. There are two Some animals and plants look like other things -- types of deceptive coloration: camouflage and they mimic them. Mimicry is another type of mimicry. deceptive coloration. It can protect the mimic from Camouflage predators or hide the mimic from prey. If mimicry was a play, there would be three characters. The Model - the species or object that is copied. The Mimic - looks and acts like another species or object. The Dupe- the tricked predator or prey. The poisonous Camouflage helps an organism blend in with its coral snake surroundings. Camouflage can be colors or and the patterns or both. When organisms are harmless camouflaged, they are harder to find. This means king snake predators have to spend a longer time finding can look a them. That's a waste of energy! When a predator is lot alike. camouflaged, it makes it easier to sneak up on or Predators surprise its prey. will avoid Blending In: Stripes or Solids? the king snake because they think it is poisonous. This type There are of mimicry is called Batesian mimicry. In lots of Batesian mimicry a harmless species mimics a different toxic or dangerous species. examples of The viceroy butterfly and monarch butterfly were once thought to camouflage. Some colors and patterns help exhibit animals blend into areas with light and shadow. Batesian The tiger's stripes help it blend into tall grass. Its mimicry golden brown strips blend in with the grass and the where a dark brown and black stripes merge with darker harmless shadows. -
Geographic Variation in Camouflage Specialization by a Decorator Crab
vol. 156, no. 1 the american naturalist july 2000 Geographic Variation in Camou¯age Specialization by a Decorator Crab John J. Stachowicz1,* and Mark E. Hay 2 1. Department of Marine Sciences, University of Connecticut, It has been argued that the ecological and evolutionary Groton, Connecticut 06340; and Institute of Marine Sciences, importance of positive interactions among species has University of North Carolina, Morehead City, North Carolina been underappreciated by most biologists (Kareiva and 28557; Bertness 1997). While many factors likely contribute to 2. School of Biology, Georgia Institute of Technology, Atlanta, Georgia 30332-0230 this bias (Boucher et al. 1982; Bertness and Callaway 1994), part of the reason for the modest attention given Submitted February 5, 1999; Accepted February 9, 2000 to the role of mutualism and other positive associations may be that the nature and strength of these interactions can be highly variable. Mutualisms that moderate local biotic or abiotic stresses may become commensal, and abstract: In North Carolina, the decorator crab Libinia dubia cam- commensalisms may become antagonistic when those ou¯ages almost exclusively with the chemically noxious alga Dictyota stresses are relaxed (e.g., Palumbi 1985; Hay 1986; Bron- menstrualis. By placing this alga on its carapace, the crab behaviorally stein 1994; Bertness and Leonard 1997; Holzapfel and sequesters the defensive chemicals of the plant and gains protection Mahall 1999; Stachowicz and Hay 1999a). Although from omnivorous consumers. However, Dictyota is absent north of many biologists recognize that biotic interactions vary in North Carolina, whereas Libinia occurs as far north as New England. outcome with local conditions, few studies examine how Crabs from three northern locations where Dictyota is absent (Rhode these changes may alter species' behaviors and evolution Island, Connecticut, and New Jersey) camou¯aged to match their environment, rather than selectively accumulating any one species. -
Predation Selects for Background Matching in the Body Colour of a Land fish
Animal Behaviour 86 (2013) 1241e1249 Contents lists available at ScienceDirect Animal Behaviour journal homepage: www.elsevier.com/locate/anbehav Natural selection in novel environments: predation selects for background matching in the body colour of a land fish Courtney L. Morgans*, Terry J. Ord Evolution and Ecology Research Centre, and the School of Biological, Earth and Environmental Sciences, University of New South Wales, Kensington, NSW, Australia article info The invasion of a novel habitat often results in a variety of new selective pressures on an individual. One Article history: pressure that can severely impact population establishment is predation. The strategies that animals use Received 8 April 2013 to minimize predation, especially the extent to which those strategies are habitat or predator specific, Initial acceptance 14 May 2013 will subsequently affect individuals’ dispersal abilities. The invasion of land by a fish, the Pacific leaping Final acceptance 6 September 2013 blenny, Alticus arnoldorum, offers a unique opportunity to study natural selection following the coloni- Available online 23 October 2013 zation of a novel habitat. Various studies have examined adaptations in respiration and locomotion, but MS. number: A13-00297R how these fish have responded to the predation regime on land was unknown. We studied five replicate populations of this fish around the island of Guam and found their body coloration converged on the Keywords: terrestrial rocky backgrounds on which the fish were most often found. Subsequent experiments adaptive evolution confirmed that this background matching significantly reduced predation. Natural selection has there- Alticus arnoldorum fore selected for background matching in the body coloration of the Pacific leaping blenny to minimize antipredator fi camouflage predation, but it is a strategy that is habitat speci c. -
Motion Dazzle and Camouflage As Distinct Anti-Predator Defenses
Stevens, M., Searle, W.T.L., Seymour, J.E., Marshall, K.L.A. and Ruxton, G.D. (2011) Motion dazzle and camouflage as distinct anti- predator defenses. BMC Biology, 9 (1). p. 81. ISSN 1741-7007 http://eprints.gla.ac.uk/59765/ Deposited on: 6 February 2012 Enlighten – Research publications by members of the University of Glasgow http://eprints.gla.ac.uk Stevens et al. BMC Biology 2011, 9:81 http://www.biomedcentral.com/1741-7007/9/81 RESEARCHARTICLE Open Access Motion dazzle and camouflage as distinct anti- predator defenses Martin Stevens1*, W Tom L Searle1, Jenny E Seymour1, Kate LA Marshall1 and Graeme D Ruxton2 Abstract Background: Camouflage patterns that hinder detection and/or recognition by antagonists are widely studied in both human and animal contexts. Patterns of contrasting stripes that purportedly degrade an observer’s ability to judge the speed and direction of moving prey (’motion dazzle’) are, however, rarely investigated. This is despite motion dazzle having been fundamental to the appearance of warships in both world wars and often postulated as the selective agent leading to repeated patterns on many animals (such as zebra and many fish, snake, and invertebrate species). Such patterns often appear conspicuous, suggesting that protection while moving by motion dazzle might impair camouflage when stationary. However, the relationship between motion dazzle and camouflage is unclear because disruptive camouflage relies on high-contrast markings. In this study, we used a computer game with human subjects detecting and capturing either moving or stationary targets with different patterns, in order to provide the first empirical exploration of the interaction of these two protective coloration mechanisms. -
Copperhead Snake on Dead Leaves, Study for Book Concealing Coloration in the Animal Kingdom Ca
June 2012 Copperhead Snake on Dead Leaves, study for book Concealing Coloration in the Animal Kingdom ca. 1910-1915 Abbott Handerson Thayer Born: Boston, Massachusetts 1849 Died: Monadnock, New Hampshire 1921 watercolor on cardboard mounted on wood panel sight 9 1/2 x 15/1/2 in. (24.1 x 39.3 cm) Smithsonian American Art Museum Gift of the heirs of Abbott Handerson Thayer 1950.2.15 Not currently on view Collections Webpage and High Resolution Image The Smithsonian American Art Museum owns eighty-seven works of art and studies by the artist Abbott Handerson Thayer made as illustrations for his book Concealing Coloration in the Animal Kingdom. Researcher Liz wanted to learn more about Thayer’s ideas on animal coloration and whether these were accepted by modern biologists. What did Thayer believe about animal coloration and its function? Abbott Handerson Thayer was an artist but had a lifelong fascination with animals and nature. He was a member of the American Ornithologists’ Union in whose publication, The Auk, his coloration studies were first published in 1896. Thayer and his son, Gerald Handerson Thayer, collaborated on the writing and illustrations for their 1909 book, Concealing-Coloration in the Animal Kingdom; an Exposition of the Laws of Disguise through Color and Pattern: Being a Summary of Abbott H. Thayer's Discoveries. Several of these original watercolors and oil paintings are on view in the Luce Foundation Center, including Blue Jays in Winter, Male Wood Duck in a Forest Pool, Red Flamingoes, Sunrise or Sunset, Roseate Spoonbill, and Roseate Spoonbills. Copperhead Snake on Dead Leaves illustrates Thayer’s contention that some animals have “ground-picturing” patterns that mimic the appearance of their surroundings.