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Relationship of Anting and Sunbathing to Molting in Wild Birds
RELATIONSHIP OF ANTING AND SUNBATHING TO MOLTING IN WILD BIRDS ELOISE F. lPOTTER AND DORIS C. HAUSER • AviAr• anting has generateda large and somewhatcontroversial body of literature, much of it based upon the behavior of captive or experi- mental birds (e.g. Ivor 1943, Whitaker 1957, Weisbrod 1971), birds treat- ing plumagewith substancesother than ants (recently with mothballs in Dubois 1969 and with lemon oil in Johnson 1971), or single oc- currencesfrom widely scatteredgeographical locations. McAtee (1954) advisedthat in searchingfor a reasonabletheory as to why birds ant only recordsfrom wild birds using ants should be examined. The authors agree with McAtee and further believe that data should be considered comparableonly when taken from a limited geographicalregion (e.g. temperateNorth America in Potter 1970). The literatureon antinghas beenreviewed several times (Groskin 1950, Whitaker 1957, Chisholm1959, Simmons1966, Potter 1970). Principal theoriesare (1) that anting birds "derive sensualpleasure from anting, possiblysexual stimulation" (Whitaker 1957); (2) that ant secretions prevent, remove, or otherwise control ectoparasiteinfestation (Groskin 1950, Dubinin in Kelso and Nice 1963, Simmons1966); (3) that ant secretionsmay be helpful in feather maintenanceby increasingflow of salivafor preening,removing stale preen oil and other lipids,or increasing feather wear resistance(Simmons 1966); and (4) that ant secretions sootheskin irritated by the emergenceof new feathers (Southern 1963, Potter 1970). Only four authors have publisheda dozen or more anting recordsinvolving wild birds usingants and takingplace in or near a single location in temperate North America. These are Brackbill (1948) from Maryland, Groskin(1950) from Pennsylvania,Potter (1970) from North Carolina, and Hauser (1973) also from North Carolina. -
Effects of Hierarchical Steepness on Grooming Patterns in Female Tibetan Macaques (Macaca Thibetana)
fevo-09-631417 February 27, 2021 Time: 15:50 # 1 ORIGINAL RESEARCH published: 04 March 2021 doi: 10.3389/fevo.2021.631417 Effects of Hierarchical Steepness on Grooming Patterns in Female Tibetan Macaques (Macaca thibetana) Dong-Po Xia1,2*†, Xi Wang2,3†, Paul A. Garber4,5, Bing-Hua Sun2,3, Lori K. Sheeran6, Lixing Sun7 and Jin-Hua Li2,3* 1 School of Life Sciences, Anhui University, Hefei, China, 2 International Collaborative Research Center for Huangshan Biodiversity and Tibetan Macaque Behavioral Ecology, Hefei, China, 3 School of Resources and Environmental Engineering, Anhui University, Hefei, China, 4 Department of Anthropology and Program in Ecology, Evolution, and Conservation Biology, University of Illinois at Urbana–Champaign, Urbana, IL, United States, 5 International Centre of Biodiversity and Primate Conservation, Dali University, Dali, China, 6 Department of Anthropology and Museum Studies, Central Washington Edited by: University, Ellensburg, WA, United States, 7 Department of Biological Sciences, Central Washington University, Ellensburg, Lucja A. Fostowicz-Frelik, WA, United States Institute of Paleobiology (PAN), Poland Hierarchical steepness, defined as status asymmetries among conspecifics living in the Reviewed by: Małgorzata Arlet, same group, is not only used as a main characteristic of animal social relationships, Adam Mickiewicz University, Poland but also represents the degree of discrepancy between supply and demand within Jundong Tian, Zhengzhou University, China the framework of biological market theory. During September and December 2011, *Correspondence: we studied hierarchical steepness by comparing variation in grooming patterns in two Dong-Po Xia groups of Tibetan macaques (Macaca thibetana), a primate species characterized by [email protected] a linear dominance hierarchy. -
Evolution of Food Sharing Behavior and Social Grooming Networks in Desmodus Rotundus with Agent-Based Models
IN PRESS, UC DAVIS McNAIR SCHOLARS JOURNAL 2019 Evolution of Food Sharing Behavior and Social Grooming Networks in Desmodus rotundus with Agent-Based Models Alery Tenorio† Faculty Mentor: Jeffrey Schank‡ College of Biological Sciences†, College of Letters and Science‡ The common vampire bat, Desmodus rotundus, is an example of a non-primate social animal that shares food. Females live in social groups of 8-12, with their offspring and perform social behaviors, such as food sharing and social grooming. Vampire bats share food with other females in their social group by regurgitating their bloodmeals to certain group members. Vampire bats groom certain group members. While social grooming has been studied, its contribution to fitness is unknown. This behavior often occurs before food sharing, possibly to identify cheats, who accept food sharing but do not share. Excluding mother-daughter interactions, social grooming and food sharing usually occurs within subgroups of social groups. These subgroups within social groups are highly associated group members of 2 to 4 and their offspring. While many studies focus on entire social groups or populations, this paper lays the groundwork for investigating whether social grooming is a mechanism for assessing whether bats will share blood meals. The proposed investigation will be conducted by producing agent-based models of vampire bat social groups. These models represent individuals that behave in essential ways like vampire bats and will allow us to characterize by emergent behavior and population-level impacts of behavior. Our goal is to determine whether blood-meal sharing can evolve given or understand of the physiology, behavior, and population structure of vampire bats. -
Anatomy Was Groomed. During a Focal Animal Sample 1974). Combining the Three Sampling Procedures A
3 Patterns and Functions of Grooming Behavior among the Common Indian Langur Monkey James J. McKenna For many primate species grooming is a predomin- These data suggest, particularly with respect to the ant and socially important behavior pattern diverse question of functions, that while grooming no doubt both in the form it can take and the social situations serves both social and hygienic functions, it does so in a within which it is initiated. While not the only behavior context apparently dictated -by social needs. It is con- that often cuts across different age and sex classes to cluded that social grooming among langur monkeys is promote cohesion, the tremendous amount of time highly integrated into almost all aspects of group life and energy invested by some species in this activity and, while not a reliable behavioral index to status suggests that as a bond-building mechanism social differentials between group members, it is important grooming has played an auxiliary if not complemen- in assessing role complexes. tary role in the evolution of primate sociality. Among primates social grooming is thought by in- Materials and Methods vestigators to provide useful information on many dif- The study group was housed in a dome-shaped ferent aspects of group life. Grooming data has been mesh enclosure approximately 35 feet high by 45 feet used to measure developmental processes in the in diameter. Starting from the enclosure floor six dif- mother-infant relationship (Hinde 1974, Kaufman ferent levels ofsitting bars and platforms, interspersed and Rosenblum 1969), to document the growing net- every three to five feet, allowed proper social and work of attachments and subgroup formations within spatial refuge. -
The Failure of the Three R's and the Future of Animal Experimentation
University of Chicago Legal Forum Volume 2006 | Issue 1 Article 7 Reduce, Refine, Replace: The aiF lure of the Three R's and the Future of Animal Experimentation Darian M. Ibrahim [email protected] Follow this and additional works at: http://chicagounbound.uchicago.edu/uclf Recommended Citation Ibrahim, Darian M. () "Reduce, Refine, Replace: The aiF lure of the Three R's and the Future of Animal Experimentation," University of Chicago Legal Forum: Vol. 2006: Iss. 1, Article 7. Available at: http://chicagounbound.uchicago.edu/uclf/vol2006/iss1/7 This Article is brought to you for free and open access by Chicago Unbound. It has been accepted for inclusion in University of Chicago Legal Forum by an authorized administrator of Chicago Unbound. For more information, please contact [email protected]. Reduce, Refine, Replace: The Failure of the Three R's and the Future of Animal Experimentation DarianM Ibrahimt The debate in animal ethics is defined by those who advocate the regulation of animal use and those who advocate its aboli- tion.' The animal welfare approach, which focuses on regulating animal use, maintains that humans have an obligation to treat animals "humanely" but may use them for human purposes.2 The animal rights approach, which focuses on abolishing animal use, argues that animals have inherent moral value that is inconsis- tent with us treating them as property.3 The animal welfare approach is the dominant model of ani- mal advocacy in the United States.4 Animal experimentation provides a fertile ground for testing this model because a unique confluence of factors make experimentation appear susceptible to meaningful regulation. -
Anting Behavior by the White-Bearded Manakin (Manacus Manacus, Pipridae): an Example of Functional Interaction in a Frugivorous Lekking Bird
Biota Neotrop., vol. 10, no. 4 Anting behavior by the White-bearded Manakin (Manacus manacus, Pipridae): an example of functional interaction in a frugivorous lekking bird César Cestari1,2 1Departamento de Zoologia, Programa de Pós-graduação em Zoologia, Universidade Estadual Paulista “Júlio de Mesquita Filho” – UNESP, Campus de Rio Claro, CEP 13506-900, Rio Claro, SP, Brasil 2Corresponding author: César Cestari, e-mail: [email protected] CESTARI, C. Anting behavior by the White-bearded Manakin (Manacus manacus, Pipridae): an example of functional interaction in a frugivorous lekking bird. Biota Neotrop. 10(4): http://www.biotaneotropica.org. br/v10n4/en/abstract?short-communication+bn02110042010. Abstract: Behavioral studies of birds have reported several functions for active anting. Maintenance of plumage and prevention from ectoparasites are some examples. In this context, anting by males may be of particular importance in a classical lek mating system, where male-male competition is common and individuals with higher fitness may be more successful at attracting of females. In the present note, I describe the anting behavior of White-bearded Manakin (Manacus manacus) and I relate it to lek breeding and feeding (frugivory) habits of the species. Males used up to seven Solenopsis sp. ants. They rubbed each small ant from 4 to 31 times on undertail feathers until the ants were degraded; ants were not eaten. Males then searched for a new ant in the court. Seeds discarded by males on their individual display courts attract herbivorous ants that are used for anting as a way to maintain feathers and fitness. I hypothesize that anting in White-bearded Manakin may increase the probability of males to attract females to their display courts. -
(Gekko Gecko LINNAEUS, 1758) Saliva on Angiogenesis
Jurnal Biologi Indonesia 13(2): 253-260 (2017) Effect of Tokay Gecko (Gekko gecko LINNAEUS, 1758) Saliva on Angiogenesis During Wound Healing Phase of Autotomized Tail in Common Sun Skink (Eutropis multifasciata KUHL, 1820) (Pengaruh Saliva Tokek (Gekko gecko, LINNEAUS 1758) Terhadap Angiogenesis Pada Fase Penyembuhan Luka Ekor Kadal Kebun (Eutropis multifasciata KUHL, 1820) Setelah Autotomi) Nurul Inayah1,2, Nyoman Puniawati Soesilo2 & Rarastoeti Pratiwi3 (1)Zoology Division, Research Center for Biology-Indonesian Institute of Sciences (LIPI) (2,3) Faculty of Biology, Gadjah Mada University Email: [email protected] Received: December 2016, Accepted: June 2017 ABSTRACT The purpose of this study was to investigate the effect of Tokay gecko saliva on morphology and angiogenesis response on the healing process of skink tail wound and also to characterize the protein profile of Gecko saliva. Twelve skinks were autotomized and wound surface of tail smeared by young gecko saliva, adult gecko saliva, and human’s saliva twice per day and control. The morphological changes of the wound surface were observed. The angiogenesis response was observed in vitro using Chorioallantois Membrane (CAM) of the ninth day's chick embryos. Protein profile of gecko saliva analyzed with SDS-PAGE. Generally, treated wound showed a better healing. Young gecko saliva able to stimulate angiogenesis in wound healing stage of sun skink tail after autotomy. Saliva protein of young and adult Gecko differences was not only in the size (or density) but also in the number of the bands. The young and adult Gecko revealed a striking consistency of protein patterns, indicating a profound physiological stability of the whole saliva. -
How Mammals Stay Healthy in Nature: the Evolution of Behaviours to Avoid Rstb.Royalsocietypublishing.Org Parasites and Pathogens
How mammals stay healthy in nature: the evolution of behaviours to avoid rstb.royalsocietypublishing.org parasites and pathogens Benjamin L. Hart and Lynette A. Hart Review School of Veterinary Medicine, University of California, Davis, CA 95616, USA BLH, 0000-0003-2342-6058; LAH, 0000-0002-7133-6535 Cite this article: Hart BL, Hart LA. 2018 How mammals stay healthy in nature: the evolution Mammals live and thrive in environments presenting ongoing threats from of behaviours to avoid parasites and parasites in the form of biting flies, ticks and intestinal worms and from pathogens as wound contaminants and agents of infectious disease. Several pathogens. Phil. Trans. R. Soc. B 373: strategies have evolved that enable animals to deal with parasites and patho- 20170205. gens, including eliminating away from the sleeping–resting areas, use of an http://dx.doi.org/10.1098/rstb.2017.0205 array of grooming techniques, use of saliva in licking, and consuming med- icinal plant-based compounds. These strategies all are species-specific and Accepted: 2 April 2018 reflect the particular environment that the animal inhabits. This article is part of the Theo Murphy meeting issue ‘Evolution of pathogen and parasite avoidance behaviours’. One contribution of 14 to a Theo Murphy meeting issue ‘Evolution of pathogen and parasite avoidance behaviours’. 1. Introduction Subject Areas: From biting flies and ticks, to intestinal worms, to wound contaminants and to behaviour, health and disease and infectious diseases, animals living in nature are in an environment that presents epidemiology, evolution an ongoing threat to health and even survival from the standpoint of parasites and pathogens. -
Records of Anting in Washington and Oregon
28Washington Birds 11:28-34 (2011)Wiles and McAllister RECORDS Of anting by biRDS in WaShingtOn anD OREgOn Gary J. Wiles Washington Department of Fish and Wildlife 600 Capitol Way North, Olympia, Washington 98501 [email protected] Kelly R. McAllister 3903 Foxhall Drive NE, Olympia, Washington 98516 [email protected] Anting is a widespread but infrequently observed stereotypic behavior noted in more than 200 bird species, the vast majority of which are pas- serines (Chisholm 1959, Simmons 1966, 1985, Craig 1999). The behavior occurs in passive and active forms (Simmons 1985). In passive anting, birds spread themselves over an ant source and allow ants to crawl through their plumage. During active anting, ants are gathered and crushed in the bill and deliberately rubbed through the plumage using preening- like motions. In this form, other objects such as millipedes, other insects, snails, fruit, flowers, other plant materials, and mothballs are occasionally substituted for ants (Whitaker 1957, Simmons 1966, Clark et al. 1990, VanderWerf 2005). Anting involves the application of the defensive secre- tions (i.e., formic acid or repugnant anal fluid) of worker ants or other aromatic chemical compounds to the feathers or skin of a bird. The purpose of anting remains unclear. Hypothesized functions include soothing irritated skin associated with feather emergence during molt, general feather maintenance, repelling ectoparasites, inhibiting fungal or bacterial growth, food preparation by removing distasteful sub- stances from prey, and pleasurable sensory stimulation (Simmons 1966, 1985, Potter and Hauser 1974, Ehrlich et al. 1986). Experimental evidence from a few species supports that anting is conducted most often during molting (Lunt et al. -
Extracellular Vesicles in Skin Wound Healing
Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 2 August 2021 doi:10.20944/preprints202108.0004.v1 Review Extracellular vesicles in skin wound healing Deimantė Narauskaitė1#, Gabrielė Vydmantaitė1#, Justina Rusteikaitė2, Revathi Sampath2, Akvilė Rudaitytė1, Ga- bija Stašytė1, María Isabel Aparicio Calvente1, Aistė Jekabsone1,2*, 1 Laboratory of Pharmaceutical Sciences, Institute of Pharmaceutical Technologies, Faculty of Pharmacy, Medical Academy, Lithuanian University of Health Sciences, Kaunas, Lithuania; D.N.- [email protected]; [email protected]; [email protected]; G.S.- [email protected]; [email protected]; [email protected] 2 Preclinical Research Laboratory for Medicinal Products, Institute of Cardiology, Lithuanian University of Health Sciences, Kaunas, Lithuania; [email protected]; [email protected] # Contributed equally * Correspondence: [email protected]; Tel.: +370 675 94455 Abstract: Each year, millions of individuals suffer from a non-healing wound, abnormal scarring, or injuries accompanied by an infection. For these cases, scientists are searching for new therapeutic interventions, from which one of the most promising is the use of extracellular vesicles (EVs). Naturally, EV-based signalling takes part in all four wound healing phases: hemostasis, inflammation, proliferation and remodelling. Such an extensive involvement of EVs suggests exploiting their action to modulate the impaired healing phase. Furthermore, -
How Birds Combat Ectoparasites
The Open Ornithology Journal, 2010, 3, 41-71 41 Open Access How Birds Combat Ectoparasites Dale H. Clayton*,1, Jennifer A. H. Koop1, Christopher W. Harbison1,2, Brett R. Moyer1,3 and Sarah E. Bush1,4 1Department of Biology, University of Utah, Salt Lake City, UT 84112, USA; 2Current address: Biology Department, Siena College, Loudonville, NY, 12211, USA; 3Current address: Providence Day School, Charlotte, NC, 28270, USA; 4Natural History Museum and Biodiversity Research Center, University of Kansas, Lawrence, Kansas 66045, USA Abstract: Birds are plagued by an impressive diversity of ectoparasites, ranging from feather-feeding lice, to feather- degrading bacteria. Many of these ectoparasites have severe negative effects on host fitness. It is therefore not surprising that selection on birds has favored a variety of possible adaptations for dealing with ectoparasites. The functional signifi- cance of some of these defenses has been well documented. Others have barely been studied, much less tested rigorously. In this article we review the evidence - or lack thereof - for many of the purported mechanisms birds have for dealing with ectoparasites. We concentrate on features of the plumage and its components, as well as anti-parasite behaviors. In some cases, we present original data from our own recent work. We make recommendations for future studies that could im- prove our understanding of this poorly known aspect of avian biology. Keywords: Grooming, preening, dusting, sunning, molt, oil, anting, fumigation. INTRODUCTION 2) Mites and ticks (Acari): many families [6-9]. As a class, birds (Aves) are the most thoroughly studied 3) Leeches: four families [10]. group of organisms on earth. -
Reading List 2012.Indd
General Reading iGAS Guidelines - Published January 2012 CLICK HERE Educational Interim UK guidelines for management of close community contacts of invasive group A streptococcal disease. Health Protection Agency, Workshops 2012 Group A Streptococcus Working Group. Communicable Disease and Public Health 2004; 7(4):354-361. CLICK HERE Keynote Presentation: Diagnosis and Complicated infections of skin and skin structures: when the infection is more than skin deep. DiNubile MJ, Lipsky, B. Journal of treatment Antimicrobial Chemotherapy, 2004, 53, Suppl. S2, ii37-ii50 of skin and soft CLICK HERE Practice guidelines for the diagnosis and management of skin and tissue infections soft tissue infections. Stevens DL et al. Clinical Infectious Disease 2005; 41:1373–1406 CLICK HERE Infections of skin and soft tissue: Outcomes of a classifi cation scheme. Eron J. Clinical Infectious Diseases 2000;31:287(A432). CLICK HERE Occurrence and antimicrobial susceptibility patterns of pathogens isolated from skin and soft tissue infections: report from the SENTRY READING Antimicrobial Surveillance Program (United States and Canada, 2000). Rennie RP et al. Diagn Microbiol Infect Dis. 2003 Apr; 45(4):287-293. LIST CLICK HERE Comparison of community and health care associated methicillin resistant Staphylococcus aureus infection. Naimi TS, et al. JAMA 2003; 290: 2976-2984 CLICK HERE Methicillin resistant S. aureus infections amoung patients in the emergency department. Moran GJ et al. The New England Journal of Medicine 2006 CLICK HERE HPR 2011;5(7): News CLICK HERE Polyclonal multiply antiobiotic-resistant methicillin-resistant Staphylococcus aureus with Panton-Valentine leucocidin in England. JAC 2009; doi: 10.1093/jac/dkp386; CLICK HERE Eff ect of antibiotics on Staphylococcus aureus producing panton- valentine leukocidin.