Forest Pest Conditions in California, 1984
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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. -
Lepidoptera: Tortricidae: Tortricinae) and Evolutionary Correlates of Novel Secondary Sexual Structures
Zootaxa 3729 (1): 001–062 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Monograph ZOOTAXA Copyright © 2013 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3729.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:CA0C1355-FF3E-4C67-8F48-544B2166AF2A ZOOTAXA 3729 Phylogeny of the tribe Archipini (Lepidoptera: Tortricidae: Tortricinae) and evolutionary correlates of novel secondary sexual structures JASON J. DOMBROSKIE1,2,3 & FELIX A. H. SPERLING2 1Cornell University, Comstock Hall, Department of Entomology, Ithaca, NY, USA, 14853-2601. E-mail: [email protected] 2Department of Biological Sciences, University of Alberta, Edmonton, Canada, T6G 2E9 3Corresponding author Magnolia Press Auckland, New Zealand Accepted by J. Brown: 2 Sept. 2013; published: 25 Oct. 2013 Licensed under a Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0 JASON J. DOMBROSKIE & FELIX A. H. SPERLING Phylogeny of the tribe Archipini (Lepidoptera: Tortricidae: Tortricinae) and evolutionary correlates of novel secondary sexual structures (Zootaxa 3729) 62 pp.; 30 cm. 25 Oct. 2013 ISBN 978-1-77557-288-6 (paperback) ISBN 978-1-77557-289-3 (Online edition) FIRST PUBLISHED IN 2013 BY Magnolia Press P.O. Box 41-383 Auckland 1346 New Zealand e-mail: [email protected] http://www.mapress.com/zootaxa/ © 2013 Magnolia Press 2 · Zootaxa 3729 (1) © 2013 Magnolia Press DOMBROSKIE & SPERLING Table of contents Abstract . 3 Material and methods . 6 Results . 18 Discussion . 23 Conclusions . 33 Acknowledgements . 33 Literature cited . 34 APPENDIX 1. 38 APPENDIX 2. 44 Additional References for Appendices 1 & 2 . 49 APPENDIX 3. 51 APPENDIX 4. 52 APPENDIX 5. -
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. -
Giovanny Fagua González
Phylogeny, evolution and speciation of Choristoneura and Tortricidae (Lepidoptera) by Giovanny Fagua González A thesis submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Systematics and Evolution Department of Biological Sciences University of Alberta © Giovanny Fagua González, 2017 Abstract Leafrollers moths are one of the most ecologically and economically important groups of herbivorous insects. These Lepidoptera are an ideal model for exploring the drivers that modulate the processes of diversification over time. This thesis analyzes the evolution of Choristoneura Lederer, a well known genus because of its pest species, in the general context of the evolution of Tortricidae. It takes an inductive view, starting with analysis of phylogenetic, biogeographic and diversification processes in the family Tortricidae, which gives context for studying these processes in the genus Choristoneura. Tectonic dynamics and niche availability play intertwined roles in determining patterns of diversification; such drivers explain the current distribution of many clades, whereas events like the rise of angiosperms can have more specific impacts, such as on the diversification rates of herbivores. Tortricidae are a diverse group suited for testing the effects of these determinants on the diversification of herbivorous clades. To estimate ancestral areas and diversification patterns in Tortricidae, a complete tribal-level dated tree was inferred using molecular markers and calibrated using fossil constraints. The time-calibrated phylogeny estimated that Tortricidae diverged ca. 120 million years ago (Mya) and diversified ca. 97 Mya, a timeframe synchronous with the rise of angiosperms in the Early-Mid Cretaceous. Ancestral areas analysis supports a Gondwanan origin of Tortricidae in the South American plate. -
Pest Categorisation of Non‐
SCIENTIFIC OPINION ADOPTED: 28 March 2019 doi: 10.2903/j.efsa.2019.5671 Pest categorisation of non-EU Choristoneura spp. EFSA Panel on Plant Health (EFSA PLH Panel), Claude Bragard, Katharina Dehnen-Schmutz, Francesco Di Serio, Paolo Gonthier, Marie-Agnes Jacques, Josep Anton Jaques Miret, Annemarie Fejer Justesen, Alan MacLeod, Christer Sven Magnusson, Juan A Navas-Cortes, Stephen Parnell, Roel Potting, Philippe Lucien Reignault, Hans-Hermann Thulke, Wopke Van der Werf, Antonio Vicent Civera, Jonathan Yuen, Lucia Zappala, Jean-Claude Gregoire, Virag Kertesz and Panagiotis Milonas Abstract The Panel on Plant Health performed a pest categorisation of non-EU Choristoneura spp. Choristoneura is a well-defined insect genus in the family Tortricidae (Insecta: Lepidoptera). Species can be identified using taxonomic keys and molecular methods. The genus includes 52 species and subspecies colonising conifers and non-conifer trees in many areas in the world, among which five species are present in the EU. The non-EU species are listed in Annex IAI of Council Directive 2000/29/EC as Choristoneura spp. (non-European). Some Choristoneura species are important defoliators in North America, mainly on conifers but also on several broadleaf tree species and on non-forest crops. Females lay eggs in batches on the needles or the leaves, and overwintering occurs at the larval stage in a silken hibernaculum. Most species are univoltine, some are bivoltine and at least one subspecies has a 2-year life cycle. Pupation occurs on the twigs of conifers or in folded leaves of broadleaf trees. The adults are strong flyers, and the larvae can disperse by ballooning. -
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. -
Scientific Names of Pest Species in Tortricidae (Lepidoptera)
RESEARCH Scientific Names of Pest Species in Tortricidae (Lepidoptera) Frequently Cited Erroneously in the Entomological Literature John W. Brown Abstract. The scientific names of several pest species in the moth meate the literature. For example, the subfamilial designation for family Tortricidae (Lepidoptera) frequently are cited erroneously in Olethreutinae (rather than Olethreutidae) was slow to be accepted contemporary entomological literature. Most misuse stems from the for many years following Obraztsov’s (1959) treatment of the group. fact that many proposed name changes appear in systematic treat- They even appear at both taxonomic levels (i.e., Olethreutinae and ments that are not seen by most members of the general entomologi- Olethreutidae) in different papers in the same issue of the Canadian cal community. Also, there is resistance among some entomologists Entomologist in the 1980s! (Volume 114 (6), 1982) Olethreutinae to conform to recently proposed changes in the scientific names of gradually was absorbed into the North America literature, espe- well-known pest species. Species names discussed in this paper are cially following publication of the Check List of the Lepidoptera Brazilian apple leafroller, Bonagota salubricola (Meyrick); western of America North of Mexico (Hodges 1983), which has served as a black-headed budworm, Acleris gloverana (Walsingham); and green standard for more than 20 years. budworm, Choristoneura retiniana (Walsingham). Generic names During preparation of a world catalog of Tortricidae (Brown discussed include those for false codling moth, Thaumatotibia leu- 2005), it became obvious to me that several taxonomically correct cotreta (Meyrick); grape berry moth, Paralobesia viteana (Clemens); combinations of important pest species were not in common use in pitch twig moth, Retinia comstockiana (Fernald); codling moth, the entomological literature. -
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. -
A Resume of Anting, with Particular Reference to A
A RESUMI? OF ANTING, WITH PARTICULAR REFERENCE TO A CAPTIVE ORCHARD ORIOLE BY LOVIE M. WHITAKER INCE Audubon (1831:7) wrote of Wild Turkeys (Meleugris gallopuvo) S rolling in “deserted” ants ’ nests (Allen, 1946)) and Gosse (1847:225) reported Tinkling Grackles (Q uiscalus niger) in nature anointing themselves with lime fruits (Chisholm, 1944), an extensive literature on the anting ac- tivities of birds has slowly evolved. The complete bibliography of anting probably would approximate 250 items, yet the purpose of the behavior re- mains unexplained. Anting may be defined as the application of foreign substances to the plum- age and possibly to the skin. These substances may be applied with the bill, or the bird may “bathe” or posture among thronging ants which invest its plumage. Among numerous explanations for the use of ants are these: (1) the bird wipes off ant acid, preparatory to eating the ant; (2) ants prey upon, and their acids repel, ectoparasites; (3) ant acids have tonic or medicinal effects on the skin of birds; (4) odor of ants attracts birds, much as dogs are drawn to ordure or cats to catnip; (5) an t s intoxicate the bird or give it unique pleasurable effects; (6) ant substances on the plumage, irradiated by sun- light, produce vitamin D, which the bird ingests during preening; (7) the bird enjoys the movement of insects in its plumage; (8) ant substances pre- vent over-drying of feather oils or give a proper surface film condition to the feathers. For discussions of these possibilities, see Chisholm (1944, 1948: 163-175)) Adlersparre (1936)) IJ zen d oorn (1952~)) Eichler (1936~)) Klein- Schmidt (in Stresemann, 1935b), L ane (1951:163-177)) Kelso (1946, 1949, 1950a, 19506, 1955 :37-39)) Brackbill (1948)) G6roudet (1948), Groskin (1950)) and McAtee (1938). -
November 2020 New UK Plant Passports From
Animal & Plant Health Agency Plant Passporting Updates No.30: November 2020 Dear plant passporters, in this edition are items on: Update on UK plant passporting starts 1st January 2021 Update on temporary Protected Zone Codes Seasonal pests and diseases on ornamentals, forestry and fruit New Plant Pest alerts – on beech and grape Plant Healthy E-Learning Modules Plant Health Risk Register and Plant Health Portal October Updates New UK Plant Passports from 1 January 2021 The Plant Health Regulation (PHR) became applicable in the UK from 14 December 2019, introducing widespread changes to the UK’s plant passport regime. This EU legislation has continued to apply to the UK during the transition period which ends on 31 December 2020. From 1 January 2021, the UK plant passport regime will change to reflect post-transition period plant health regulation. Summary of PP changes are: no flag add ‘UK’ in front of the word ‘plant passport’ Protected zones (PZ) will cease and PZ pests will either become GB quarantine pests (absent throughout GB) or Pest Free Areas (PFA) pests (absent in only part of GB); this is an internationally recognised approach Country of origin requirements broadly same as the EU’s except to enhance bio-security, some high risk hosts of Xylella fastidiosa and plants of Plane can only be labelled ‘GB’ at part D on a plant passport one year post importation. They can still be moved in the first year after import on a PP with the original country of origin in Part D See the factsheet for more details of what will be changing for Plant Passports (PP), including images of PP and what actions GB businesses need to take to be ready for 1 January. -
UNIVERSITY of CALIFORNIA RIVERSIDE Causes And
UNIVERSITY OF CALIFORNIA RIVERSIDE Causes and Consequences of Parasitism in the California Fiddler Crab, Uca Crenulata A Dissertation submitted in partial satisfaction of the requirements for the degree of Doctor of Philosophy in Evolution, Ecology, and Organismal Biology by Adrienne Brooke Mora December 2013 Dissertation Committee: Dr. Marlene Zuk, Chairperson Dr. Daphne Fairbairn Dr. Bradley Mullens Copyright by Adrienne Brooke Mora 2013 The Dissertation of Adrienne Brooke Mora is approved: _______________________________________________ _______________________________________________ _______________________________________________ Committee Chairperson University of California, Riverside ! ACKNOWLEDGEMENTS I owe a large debt of gratitude to the many people who contributed to the completion of this dissertation. First and foremost, I would like to thank my advisor, Dr. Marlene Zuk. Marlene, you always encouraged me to push myself and taught me to develop my own voice and mind. You were also a strong advocate for my research, and with your support I was inspired to reach beyond my comfort zone and take on new challenges that greatly contributed to my intellectual and personal growth. I would also like to thank Dr. Daphne Fairbairn for her help and guidance throughout my graduate career. Daphne, you gave me great insights into the life of an academic, and helped me learn to think critically and set high standards for myself. When my working space was jeopardized, you jumped in and offered your lab space to me. I am forever grateful to you for your support during this time, as I would not have been able to complete my experiments were it not for you. I consider both you and Marlene to be great role models. -
Owl Monkeys ( Aotus Spp.) Perform Self- and Social Anointing in Captivity
Original Article Folia Primatol 2014;85:119–134 Received: April 16, 2013 DOI: 10.1159/000359970 Accepted after revision: January 20, 2014 Published online: May 14, 2014 Owl Monkeys ( Aotus spp.) Perform Self- and Social Anointing in Captivity a a a, b Jay P. Jefferson Elizabeth Tapanes Sian Evans a b Florida International University, and DuMond Conservancy for Primates and Tropical Forests, Miami, Fla. , USA Key Words Owl monkeys · Aotus · Anointing · Millipede · Fur rubbing Abstract Several species of primates, including owl monkeys (Aotus spp.), anoint by rubbing their fur with odiferous substances. Previous research has shown that capuchin mon- keys (Cebus and Sapajus) anoint socially by rubbing their bodies together in groups of two or more while anointing. Owl monkeys housed at the DuMond Conservancy have been observed to anoint over the last 10 years, and we report detailed new information on the anointing behavior of this population, including descriptions of social anointing which occurs frequently. We first investigated the occurrence of self-anointing in 35 Aotus spp. presented with millipedes. Detailed descriptions regarding body regions anointed were obtained for all anointers (n = 28). The median duration for a self-anoint- ing bout was 3.6 min (range from approx. 2 s to 14.15 min). While the latency and length of anointing bouts showed considerable interindividual differences, no statistically sig- nificant differences were found between sexes, wild- or captive-born owl monkeys or across age groups. However, we found the lower back and tail were anointed at a rate significantly greater than other body parts, but there were no differences in these patterns across sex or wild- or captive-born owl monkeys.