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Field Guides Tour Report Thanksgiving in Jamaica 2019 Nov 24, 2019 to Nov 30, 2019 Cory Gregory & Dwane Swaby For our tour description, itinerary, past triplists, dates, fees, and more, please VISIT OUR TOUR PAGE. Jamaica has such a long list of amazingly beautiful and colorful birds that it's hard to pick a favorite. Close to the top of the list however surely was this Jamaican Spindalis, a species only found in Jamaica. Photo by guide Cory Gregory. Sitting between South America and Cuba, the Caribbean nation of Jamaica was a fantastic place for us to enjoy the warm weather, the plethora of unique and fascinating birds, the relaxed lifestyle, and escaping the holiday hustle and bustle. With the birdy and historical Green Castle Estate as our home base, we made a variety of daytrips and had the luxury of returning back to the same place every night! Our day trips took us to a variety of birding hotspots and between them all, we saw a vast majority of the avifauna that this island nation has to offer. Even in driving from Montego Bay to Green Castle on our first day, we were surrounded with attention-grabbing species like Magnificent Frigatebirds gliding overhead, Zenaida Doves sitting on the wires, and even a small gathering of the rare West Indian Whistling-Ducks in Discovery Bay! Our first day at Green Castle was our first foray into the forests and we quickly connected with a fun collection of endemic species like the showy Streamertail, Jamaican Woodpecker, Sad Flycatcher, White-chinned Thrush, Jamaican Spindalis, Orangequit, and many others. -
Castle Green Bird List
GREEN CASTLE ESTATE Bird List Birds seen on recent tours during November – April | In one week we can expect around 120 species. E=Endemic | ES=Endemic Subspecies | I=Introduced Some of the species below are very unusual however they have been included for completeness. Jamaica has recorded over 300 species and the birds below are the most frequently encountered, however we cannot guarantee what we will or will not see, that’s birding! West Indian Whistling-Duck Lesser Yellowlegs Greater Antillean Elaenia (ES) Blue-winged Teal Whimbrel Jamaican Pewee (E) Northern Shoveler Ruddy Turnstone Sad Flycatcher (E) Ring-necked Duck Red Knot Rufous-tailed Flycatcher (E) Lesser Scaup Sanderling Stolid Flycatcher (ES) Masked Duck Semipalmated Sandpiper Gray Kingbird Ruddy Duck Western Sandpiper Loggerhead Kingbird (ES) Least Grebe Least Sandpiper Jamaican Becard (E) Pied-billed Grebe White-rumped Sandpiper Jamaican Vireo (E) White-tailed Tropicbird Baird's Sandpiper Blue Mountain Vireo (E) Magnificent Frigatebird Stilt Sandpiper Black-whiskered Vireo Brown Booby Short-billed Dowitcher Jamaican Crow (E) Brown Pelican Laughing Gull Caribbean Martin American Bittern Least Tern Tree Swallow Least Bittern Gull-billed Tern Northern Rough-winged Swallow Great Blue Heron Caspian Tern Cave Swallow (ES) Great Egret Royal Tern Barn Swallow Snowy Egret Sandwich Tern Rufous-throated Solitaire (ES) Little Blue Heron Rock Pigeon (I) White-eyed Thrush (E) Tricolored Heron White-crowned Pigeon White-chinned Thrush (E) Reddish Egret Plain Pigeon (ES) Gray Catbird Cattle -
Acoustic Communication in the Nocturnal Lepidoptera
Chapter 6 Acoustic Communication in the Nocturnal Lepidoptera Michael D. Greenfield Abstract Pair formation in moths typically involves pheromones, but some pyra- loid and noctuoid species use sound in mating communication. The signals are generally ultrasound, broadcast by males, and function in courtship. Long-range advertisement songs also occur which exhibit high convergence with commu- nication in other acoustic species such as orthopterans and anurans. Tympanal hearing with sensitivity to ultrasound in the context of bat avoidance behavior is widespread in the Lepidoptera, and phylogenetic inference indicates that such perception preceded the evolution of song. This sequence suggests that male song originated via the sensory bias mechanism, but the trajectory by which ances- tral defensive behavior in females—negative responses to bat echolocation sig- nals—may have evolved toward positive responses to male song remains unclear. Analyses of various species offer some insight to this improbable transition, and to the general process by which signals may evolve via the sensory bias mechanism. 6.1 Introduction The acoustic world of Lepidoptera remained for humans largely unknown, and this for good reason: It takes place mostly in the middle- to high-ultrasound fre- quency range, well beyond our sensitivity range. Thus, the discovery and detailed study of acoustically communicating moths came about only with the use of electronic instruments sensitive to these sound frequencies. Such equipment was invented following the 1930s, and instruments that could be readily applied in the field were only available since the 1980s. But the application of such equipment M. D. Greenfield (*) Institut de recherche sur la biologie de l’insecte (IRBI), CNRS UMR 7261, Parc de Grandmont, Université François Rabelais de Tours, 37200 Tours, France e-mail: [email protected] B. -
Jamaica Boswell Trip Report 23Rd to 28Th March 2018 (6 Days)
Jamaica Boswell Trip Report 23rd to 28th March 2018 (6 days) Crested Quail-Dove by Rich Lindie Trip report compiled by Tour Leader: Rich Lindie Trip Report – RBL Jamaica – Boswell Tailor-made tour 2018 2 ------------------------------------------------------------------------------------------------------------------- Jamaican Tody by Rich Lindie For those of us who arrived in-country a night in advance, the Jamaican birding adventures began within the confines of Kingston, where, it seems, sightings of endemic parrots and unknown Myiarchus flycatchers were a highlight. Not to downplay the city itself which, although congested and rather lacklustre in many parts, certainly does have a few intriguing sites, as well as a great deal of goings-on to see - especially while whiling away time in slow traffic. Well, for the unlucky, anyway. Once out of the city, and along one of the island's many narrow and winding roads, the scenery and pace was distinctly different though interesting, too, though I'm sure it was with a great sense of calm and welcome that the first day ended at the somewhat charming Greencastle Estate. Well, again, it was for me. Not least of which because we all got to meet up as a group for the first time! Celebratory drinks, introductions and reunions, and plenty of stories to follow. But soon it was time for business, and the next morning saw us up bright and early, and off into the forest, where a host of super endemics awaited. Even if Dwayne didn't. Kicking things off in real style, one of the first birds we encountered was an obliging Jamaican Oriole, while a supporting cast that included male Orangequits, a pair of Jamaican Woodpeckers and a Black-faced Grassquit was also much enjoyed. -
Moth Hearing and Sound Communication
J Comp Physiol A (2015) 201:111–121 DOI 10.1007/s00359-014-0945-8 REVIEW Moth hearing and sound communication Ryo Nakano · Takuma Takanashi · Annemarie Surlykke Received: 17 July 2014 / Revised: 13 September 2014 / Accepted: 15 September 2014 / Published online: 27 September 2014 © Springer-Verlag Berlin Heidelberg 2014 Abstract Active echolocation enables bats to orient notion of moths predominantly being silent. Sexual sound and hunt the night sky for insects. As a counter-measure communication in moths may apply to many eared moths, against the severe predation pressure many nocturnal perhaps even a majority. The low intensities and high fre- insects have evolved ears sensitive to ultrasonic bat calls. quencies explain that this was overlooked, revealing a bias In moths bat-detection was the principal purpose of hear- towards what humans can sense, when studying (acoustic) ing, as evidenced by comparable hearing physiology with communication in animals. best sensitivity in the bat echolocation range, 20–60 kHz, across moths in spite of diverse ear morphology. Some Keywords Co-evolution · Sensory exploitation · eared moths subsequently developed sound-producing Ultrasound · Echolocating bats · Predator-prey organs to warn/startle/jam attacking bats and/or to com- municate intraspecifically with sound. Not only the sounds for interaction with bats, but also mating signals are within Introduction the frequency range where bats echolocate, indicating that sound communication developed after hearing by “sensory Insect hearing and sound communication is a fascinating exploitation”. Recent findings on moth sound communica- subject, where the combination of many classical studies tion reveal that close-range (~ a few cm) communication and recent progress using new technological and molecular with low-intensity ultrasounds “whispered” by males dur- methods provide an unsurpassed system for studying and ing courtship is not uncommon, contrary to the general understanding the evolution of acoustic communication, intraspecific as well as between predator and prey. -
The Conservation Status of the World's Reptiles
Marquette University e-Publications@Marquette Biological Sciences Faculty Research and Publications Biological Sciences, Department of 1-2013 The Conservation Status of the World’s Reptiles Tony Gamble Follow this and additional works at: https://epublications.marquette.edu/bio_fac Part of the Biology Commons Marquette University e-Publications@Marquette Biological Sciences Faculty Research and Publications/College of Arts and Sciences This paper is NOT THE PUBLISHED VERSION; but the author’s final, peer-reviewed manuscript. The published version may be accessed by following the link in the citation below. Biological Conservation, Vol. 157, (January 2013): 372-385. DOI. This article is © Elsevier and permission has been granted for this version to appear in e-Publications@Marquette. Elsevier does not grant permission for this article to be further copied/distributed or hosted elsewhere without the express permission from Elsevier. The Conservation Status of the World’s Reptiles Monika Böhm Institute of Zoology, Zoological Society of London, Regent’s Park, London NW1 4RY, UK Ben Collen Institute of Zoology, Zoological Society of London, Regent’s Park, London NW1 4RY, UK Jonathan E.M. Baillie Conservation Programmes, Zoological Society of London, Regent’s Park, London NW1 4RY, UK Philip Bowles IUCN – CI Biodiversity Assessment Unit, Conservation International, 2011 Crystal Drive Ste 500, Arlington, VA Janice Chanson Species Programme, IUCN, Rue Mauverney 28, 1196 Gland, Switzerland IUCN – CI Biodiversity Assessment Unit, c/o 130 Weatherall Road, Cheltenham 3192, Vic., Australia Neil Cox IUCN – CI Biodiversity Assessment Unit, Conservation International, 2011 Crystal Drive Ste 500, Arlington, VA Species Programme, IUCN, Rue Mauverney 28, 1196 Gland, Switzerland Geoffrey Hammerson NatureServe, 746 Middlepoint Road, Port Townsend, WA Michael Hoffmann IUCN SSC Species Survival Commission, c/o United Nations Environment Programme World Conservation Monitoring Centre, 219 Huntingdon Road, Cambridge CB3 0DL, UK Suzanne R. -
Bird Species I Have Seen World List
bird species I have seen U.K tally: 279 US tally: 393 Total world: 1,496 world list 1. Abyssinian ground hornbill 2. Abyssinian longclaw 3. Abyssinian white-eye 4. Acorn woodpecker 5. African black-headed oriole 6. African drongo 7. African fish-eagle 8. African harrier-hawk 9. African hawk-eagle 10. African mourning dove 11. African palm swift 12. African paradise flycatcher 13. African paradise monarch 14. African pied wagtail 15. African rook 16. African white-backed vulture 17. Agami heron 18. Alexandrine parakeet 19. Amazon kingfisher 20. American avocet 21. American bittern 22. American black duck 23. American cliff swallow 24. American coot 25. American crow 26. American dipper 27. American flamingo 28. American golden plover 29. American goldfinch 30. American kestrel 31. American mag 32. American oystercatcher 33. American pipit 34. American pygmy kingfisher 35. American redstart 36. American robin 37. American swallow-tailed kite 38. American tree sparrow 39. American white pelican 40. American wigeon 41. Ancient murrelet 42. Andean avocet 43. Andean condor 44. Andean flamingo 45. Andean gull 46. Andean negrito 47. Andean swift 48. Anhinga 49. Antillean crested hummingbird 50. Antillean euphonia 51. Antillean mango 52. Antillean nighthawk 53. Antillean palm-swift 54. Aplomado falcon 55. Arabian bustard 56. Arcadian flycatcher 57. Arctic redpoll 58. Arctic skua 59. Arctic tern 60. Armenian gull 61. Arrow-headed warbler 62. Ash-throated flycatcher 63. Ashy-headed goose 64. Ashy-headed laughing thrush (endemic) 65. Asian black bulbul 66. Asian openbill 67. Asian palm-swift 68. Asian paradise flycatcher 69. Asian woolly-necked stork 70. -
Molecular Studies of South American Teiid Lizards (Teiidae: Squamata) from Deep Time to Shallow Divergences Derek B
Brigham Young University BYU ScholarsArchive All Theses and Dissertations 2016-06-01 Molecular Studies of South American Teiid Lizards (Teiidae: Squamata) from Deep Time to Shallow Divergences Derek B. Tucker Brigham Young University Follow this and additional works at: https://scholarsarchive.byu.edu/etd Part of the Biology Commons BYU ScholarsArchive Citation Tucker, Derek B., "Molecular Studies of South American Teiid Lizards (Teiidae: Squamata) from Deep Time to Shallow Divergences" (2016). All Theses and Dissertations. 6419. https://scholarsarchive.byu.edu/etd/6419 This Dissertation is brought to you for free and open access by BYU ScholarsArchive. It has been accepted for inclusion in All Theses and Dissertations by an authorized administrator of BYU ScholarsArchive. For more information, please contact [email protected], [email protected]. Molecular Studies of South American Teiid Lizards (Teiidae: Squamata) from Deep Time to Shallow Divergences Derek B. Tucker A dissertation submitted to the faculty of Brigham Young University in partial fulfillment of the requirements for the degree of Doctor of Philosophy Jack W. Sites, Jr., Chair Guarino R. Colli Seth M. Bybee Leigh A. Johnson Duke S. Rogers Department of Biology Brigham Young University June 2016 Copyright © 2016 Derek B. Tucker All Rights Reserved ABSTRACT Molecular Studies of South American Teiid Lizards (Teiidae: Squamata) from Deep Time to Shallow Divergences Derek B. Tucker Department of Biology, BYU Doctor of Philosophy I focus on phylogenetic relationships of teiid lizards beginning with generic and species relationship within the family, followed by a detailed biogeographical examination of the Caribbean genus Pholidoscelis, and end by studying species boundaries and phylogeographic patterns of the widespread Giant Ameiva Ameiva ameiva. -
Proceedings of the Forteenth Symposium on the Natural History of the Bahamas
PROCEEDINGS OF THE FORTEENTH SYMPOSIUM ON THE NATURAL HISTORY OF THE BAHAMAS Edited by Craig Tepper and Ronald Shaklee Conference Organizer Thomas Rothfus Gerace Research Centre San Salvador Bahamas 2011 Cover photograph – “Iggie the Rock Iguana” courtesy of Ric Schumacher Copyright Gerace Research Centre All Rights Reserved No part of this publication may be reproduced or transmitted in any form or by any means electronic or mechanical, including photocopy, recording or information storage or retrieval system without permission in written form. Printed at the Gerace Research Centre ISBN 0-935909-95-8 The 14th Symposium on the Natural History of the Bahamas VISITORS TO RAM’S HORN, PITHECELLOBIUM KEYENSE BRITT. EX BRITT. AND ROSE, ON SAN SALVADOR ISLAND, THE BAHAMAS Nancy B. Elliott1, Carol L. Landry2, Lee B. Kass3, and Beverly J. Rathcke4 1Department of Biology Siena College Loudonville, NY 11211 2Department of Evolution, Ecology and Organismal Biology The Ohio State University Mansfield, OH 44906 3The L. H. Bailey Hortorium, Department of Plant Biology Cornell University Ithaca, NY 14953 4Department of Ecology and Evolutionary Biology University of Michigan Ann Arbor, MI 48109 ABSTRACT and the pierid Phoebis agarithe were seen more than once. One dipteran, Callitrega macellaria, We made observations on individuals of and two nectivorous birds, the bananaquit, Pithecellobium keyense (ram’s horn) in flower on Coereba flaveola, and the Bahama woodstar, San Salvador during the following periods: late Calliphlox evelynae, were occasional visitors. December 2002 to early January 2003, October 2007 and December 2010. Most of the visitors we INTRODUCTION saw belonged to the insect orders Hymenoptera and Lepidoptera. -
Field Guide Invasives Pests in Caribbean Ukots Part 1
FIELD GUIDE TO INVASIVE ALIEN PLANT PESTS IN THE CARIBBEAN UK OVERSEAS TERRITORIES PART 1 – INTRODUCTION Chris Malumphy, Sharon Reid, Rachel Down, Jackie Dunn and Debbie Collins UKOT Caribbean Invasive Plant Pest Field Guide FIELD GUIDE TO INVASIVE ALIEN PLANT PESTS IN THE CARIBBEAN UK OVERSEAS TERRITORIES Part 1 Introduction Chris Malumphy, Sharon Reid, Rachel Down, Jackie Dunn and Debbie Collins Second Edition Fera Science Ltd., National Agri-food Innovation Campus, Sand Hutton, York, YO41 1LZ, United Kingdom https://fera.co.uk/ Published digitally: April 2018. Second edition published digitally: April 2019. Divided into 6 parts to enable easier download © Crown copyright 2018-19 Suggested citation: Malumphy, C., Reid, S., Down, R., Dunn., J. & Collins, D. 2019. Field Guide to Invasive Alien Plant Pests in the Caribbean UK Overseas Territories. 2nd Edition. Part 1 – Introduction. Defra/Fera. 30 pp. Frontispiece Top row: Giant African land snail Lissachatina fulica © C. Malumphy; Mediterranean fruit fly Ceratitis capitata © Crown copyright; Sri Lankan weevil, Myllocerus undecimpustulatus undatus adult © Gary R. McClellan. Second row: Cactus moth Cactoblastis cactorum caterpillar © C. Malumphy; Cottony cushion scale Icerya purcashi © Crown copyright; Red palm mite Raoiella indica adults © USDA. Third row: Tomato potato psyllid Bactericera cockerelli © Fera; Cotton bollworm Helicoverpa armigera © Crown copyright; Croton scale Phalacrococcus howertoni © C. Malumphy. Bottom row: Red palm weevil Rhynchophorus ferrugineus © Fera; Tobacco whitefly -
Empyreuma Species and Species Limits: Evidence from Morphology and Molecules (Arctiidae: Arctiinae: Ctenuchini)
iuumal of the Lepidopterists' Society ,58 (1), 2004, 21-32 EMPYREUMA SPECIES AND SPECIES LIMITS: EVIDENCE FROM MORPHOLOGY AND MOLECULES (ARCTIIDAE: ARCTIINAE: CTENUCHINI) SUSAN J, WELLER,l REBECCA B, SIMMONS2 AND ANDERS L. CARLSON3 ABSTRACT. Species limits within Empyreurrw are addressed using a morphological study of male and female genitalia and sequence data from the mitodlOndrial gene COl. Currently, four species are recognized: E. pugione (L.), E, affinis Rothschild, E, heros Bates, E, anassa Forbes, Two cntities can be readily distinguished, the Jamaican E. anassa and a widespread E. pugione-complex, based on adult morphology. Neither E. affinis nor E, heros can be distingUished by coloration or genitalic differences, Analysis of COl haplotypes suggests that E, affinis is not genetically distinct from E. pugione « 1% sequence divergence); however, the population from the Bahamas, E, heros, is differentiated from other haplotypes with an uncorrected sequence divergence of 5%. We place E. affinis Rothschild, 1912 as a new synonym of E. pugione Hubner 1818, and recognize three spedes: E. anassa, E. pugione, and E. heros. This paper includes a revised synonymic checklist of species and a redescription of the genus, with notes on biology, and with illustrations of male genitalia, female genitalia, wing venation, and abdominal sclerites. Additional key words: Caribbean fauna, Greater Antilles, mimicry, phylogeography, systematics. The tiger moth genus Empyreuma Hubner (Arcti affinis as a junior synonym of E. pugione. Bates (1934) idae: Arctiinae: Ctenuchini) (Hubner 1818) is endemic subsequently described E. heros from the Bahamas, but to the Greater Antilles of the Caribbean, and has ex he did not provide figures or diagnostiC features that panded its distribution into Florida (Adam & Goss separate it from previously described species. -
Research Article Immature Stages and Life Cycle of the Wasp Moth, Cosmosoma Auge (Lepidoptera: Erebidae: Arctiinae) Under Laboratory Conditions
Hindawi Publishing Corporation Psyche Volume 2014, Article ID 328030, 6 pages http://dx.doi.org/10.1155/2014/328030 Research Article Immature Stages and Life Cycle of the Wasp Moth, Cosmosoma auge (Lepidoptera: Erebidae: Arctiinae) under Laboratory Conditions Gunnary León-Finalé and Alejandro Barro Department of Animal and Human Biology, Faculty of Biology, University of Havana, Calle 25 No. 455 Entre I y J, Vedado, Municipio Plaza, 10400 Ciudad de la Habana, Cuba Correspondence should be addressed to Alejandro Barro; [email protected] Received 24 February 2014; Revised 20 May 2014; Accepted 29 May 2014; Published 9 July 2014 Academic Editor: Kent S. Shelby Copyright © 2014 G. Leon-Final´ e´ and A. Barro. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Cosmosoma auge (Linnaeus 1767) (Lepidoptera: Erebidae) is a Neotropical arctiid moth common in Cuban mountainous areas; however, its life cycle remains unknown. In this work, C. auge life cycle is described for the first time; also, immature stages are describedusingaCubanpopulation.LarvaewereobtainedfromgravidwildfemalescaughtinVinales˜ National Park and were fed with fresh leaves of its host plant, the climbing hempweed Mikania micrantha Kunth (Asterales: Asteraceae), which is a new host plant record. Eggs are hemispherical and hatching occurred five days after laying. Larval period had six instars and lasted between 20 and 22 days. First and last larval stages are easily distinguishable from others. First stage has body covered by chalazae and last stage has body covered by verrucae as other stages but has a tuft on each side of A1 and A7.