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National Monitoring Program for Biodiversity and Non-Indigenous Species in Egypt
UNITED NATIONS ENVIRONMENT PROGRAM MEDITERRANEAN ACTION PLAN REGIONAL ACTIVITY CENTRE FOR SPECIALLY PROTECTED AREAS National monitoring program for biodiversity and non-indigenous species in Egypt PROF. MOUSTAFA M. FOUDA April 2017 1 Study required and financed by: Regional Activity Centre for Specially Protected Areas Boulevard du Leader Yasser Arafat BP 337 1080 Tunis Cedex – Tunisie Responsible of the study: Mehdi Aissi, EcApMEDII Programme officer In charge of the study: Prof. Moustafa M. Fouda Mr. Mohamed Said Abdelwarith Mr. Mahmoud Fawzy Kamel Ministry of Environment, Egyptian Environmental Affairs Agency (EEAA) With the participation of: Name, qualification and original institution of all the participants in the study (field mission or participation of national institutions) 2 TABLE OF CONTENTS page Acknowledgements 4 Preamble 5 Chapter 1: Introduction 9 Chapter 2: Institutional and regulatory aspects 40 Chapter 3: Scientific Aspects 49 Chapter 4: Development of monitoring program 59 Chapter 5: Existing Monitoring Program in Egypt 91 1. Monitoring program for habitat mapping 103 2. Marine MAMMALS monitoring program 109 3. Marine Turtles Monitoring Program 115 4. Monitoring Program for Seabirds 118 5. Non-Indigenous Species Monitoring Program 123 Chapter 6: Implementation / Operational Plan 131 Selected References 133 Annexes 143 3 AKNOWLEGEMENTS We would like to thank RAC/ SPA and EU for providing financial and technical assistances to prepare this monitoring programme. The preparation of this programme was the result of several contacts and interviews with many stakeholders from Government, research institutions, NGOs and fishermen. The author would like to express thanks to all for their support. In addition; we would like to acknowledge all participants who attended the workshop and represented the following institutions: 1. -
Appendicularia of CTAW
APPENDICULARIA APPENDICULARIA a b Fig. 26. Oikopleura albicans (Leuckart, 1854), a commonly occurring appendicularian species: a, dorsal view; b, lateral view. (Scale bar = 0.1 mm). [after T. Prentiss, reproduced with permission, from Alldredge 1976] Appendicularians are small free swimming planktonic tunicates, their bodies consisting of a short trunk and a tail (containing the notochord cells) which is present through the life of the individual. Glandular (oikoplast) epithelium on the trunk secretes the mucous house which encloses the whole or part of the body and contains the complex filters which strain food from the water driven through them (Deibel 1998; Flood & Deibel 1998). Unlike other tunicates, there is no peribranchial cavity and a pair of pharyngeal perforations (spiracles) surrounded by a ring of cilia open directly to the exterior from the floor of the pharynx. The early studies of these organisms, begun with Chamisso's description of Appendicularia flagellum Chamisso, 1821, were confounded by questions of its phylogenetic affinity. Chamisso classified his species with medusoids, Mertens (1830) with molluscs, and Quoy & Gaimard (1833) with zoophytes. Only in 1851 were appendicularians correctly assigned to the Tunicata by Huxley. At the time of this placement, the existence of more than one taxon was only just beginning to be recognised, and despite Huxley's work, they were not universally regarded as adult organisms—some authors still insisting that they were ascidian larvae or a free swimming generation of the sessile ascidians (Fenaux 1993). Subsequently, these questions were resolved by the work of Fol (1872) on material from the Straits of Messina, which forms the basis of later studies on the large collections of the great expeditions of the 19th century that revealed their true diversity in the oceanic plankton. -
Canestro 07Devbio Oikopleura Retinoic Acid Chordate.Pdf
Developmental Biology 305 (2007) 522–538 www.elsevier.com/locate/ydbio Development of a chordate anterior–posterior axis without classical retinoic acid signaling ⁎ Cristian Cañestro, John H. Postlethwait Institute of Neuroscience, University of Oregon, Eugene, OR 97403, USA Received for publication 28 November 2006; revised 18 February 2007; accepted 26 February 2007 Available online 2 March 2007 Abstract Developmental signaling by retinoic acid (RA) is thought to be an innovation essential for the origin of the chordate body plan. The larvacean urochordate Oikopleura dioica maintains a chordate body plan throughout life, and yet its genome appears to lack genes for RA synthesis, degradation, and reception. This suggests the hypothesis that the RA-machinery was lost during larvacean evolution, and predicts that Oikopleura development has become independent of RA-signaling. This prediction raises the problem that the anterior–posterior organization of a chordate body plan can be developed without the classical morphogenetic role of RA. To address this problem, we performed pharmacological treatments and analyses of developmental molecular markers to investigate whether RA acts in anterior–posterior axial patterning in Oikopleura embryos. Results revealed that RA does not cause homeotic posteriorization in Oikopleura as it does in vertebrates and cephalochordates, and showed that a chordate can develop the phylotypic body plan in the absence of the classical morphogenetic role of RA. A comparison of Oikopleura and ascidian evidence suggests that the lack of RA-induced homeotic posteriorization is a shared derived feature of urochordates. We discuss possible relationships of altered roles of RA in urochordate development to genomic events, such as rupture of the Hox-cluster, in the context of a new understanding of chordate phylogeny. -
Study of Dental Fluorosis in Subjects Related to a Phosphatic Fertilizer
Indian Journal of Geo Marine Sciences Vol. 46 (07), July 2017, pp. 1371-1380 Diversity and abundance of epipelagic larvaceans and calanoid copepods in the eastern equatorial Indian Ocean during the spring inter-monsoon Kaizhi Li, Jianqiang Yin*, Yehui Tan, Liangmin Huang & Gang Li Key Laboratory of Tropical Marine Bio-resources and Ecology, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China *[E-mail: [email protected]] Received 20 August 2015; revised 29 September 2015 This study investigated the species composition, distribution and abundance of larvaceans and calanoid copepods in the eastern equatorial Indian Ocean. In total, 25 species of larvaceans and 69 species of calanoid copepods were identified in the study area. Although the average diversity and evenness indexes of larvaceans were lower than those of calanoid copepods, the abundance of larvaceans was higher than that of calanoids with means of 40.1±14.9 ind m-3 and 28.4±9.1 ind m-3, respectively. Larvacean community was numerically dominated by Oikopleura fusiformis, Oikopleura longicauda, Oikopleura cophocerca, Fritillaria formica and Fritillaria pellucida, accounting for 83% of total larvacean abundance. The calanoid community was dominated by the following five species, represented 61% of calanoid copepods: Clausocalanus furcatus, Clausocalanus farrani, Acartia negligens, Acrocalanus longicornis as well as the copepodite stage of Euchaeta spp. This study highlights that the importance of larvaceans in the eastern equatorial Indian Ocean. [Keywords: Appendicularians, Calanoids, Water mass, Monsoon, Indian Ocean] Introduction It has been clear that small organisms of marine Clausocalanus) and the cyclopoid genera (such as zooplankton have historically been under-sampled by Oithona, Oncaea and Corycaeus1). -
Insects of Western North America 4. Survey of Selected Insect Taxa of Fort Sill, Comanche County, Oklahoma 2
Insects of Western North America 4. Survey of Selected Insect Taxa of Fort Sill, Comanche County, Oklahoma 2. Dragonflies (Odonata), Stoneflies (Plecoptera) and selected Moths (Lepidoptera) Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Survey of Selected Insect Taxa of Fort Sill, Comanche County, Oklahoma 2. Dragonflies (Odonata), Stoneflies (Plecoptera) and selected Moths (Lepidoptera) by Boris C. Kondratieff, Paul A. Opler, Matthew C. Garhart, and Jason P. Schmidt C.P. Gillette Museum of Arthropod Diversity Department of Bioagricultural Sciences and Pest Management Colorado State University, Fort Collins, Colorado 80523 March 15, 2004 Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Cover illustration (top to bottom): Widow Skimmer (Libellula luctuosa) [photo ©Robert Behrstock], Stonefly (Perlesta species) [photo © David H. Funk, White- lined Sphinx (Hyles lineata) [photo © Matthew C. Garhart] ISBN 1084-8819 This publication and others in the series may be ordered from the C.P. Gillette Museum of Arthropod Diversity, Department of Bioagricultural Sciences, Colorado State University, Fort Collins, Colorado 80523 Copyrighted 2004 Table of Contents EXECUTIVE SUMMARY……………………………………………………………………………….…1 INTRODUCTION…………………………………………..…………………………………………….…3 OBJECTIVE………………………………………………………………………………………….………5 Site Descriptions………………………………………….. METHODS AND MATERIALS…………………………………………………………………………….5 RESULTS AND DISCUSSION………………………………………………………………………..…...11 Dragonflies………………………………………………………………………………….……..11 -
Arriving at the Whole Story President Chris Hepburn, Vice President Michael Clarke, Secretary Katherine Howard, Treasurer
NEWSLETTER Newton’s land trust working to preserve open space since 1961 WINTER ISSUE NEWTONCONSERVATORS.ORG • WINTER 2020-2021 2020 Officers and Directors Ted Kuklinski, Arriving at the Whole Story President Chris Hepburn, Vice President Michael Clarke, Secretary Katherine Howard, Treasurer AnnaMaria Abernathy David Backer Peter Barrer Barbara Bates Dan Brody Bonnie Carter Margaret Doris ALL PHOTOS THIS ARTICLE: SAM JAFFE Henry Finch Left to right: Cecropia Giant Silk Moth, Hyalophora cecropia: found on buttonbush,Boston MA. Maurice Gilmore Elm Sphinx, Ceratomia amyntor: Mimic of dried elm leaves, found at Oxbow National Wildlife Refuge, Harvard MA. Daniel Green Abbott’s Sphinx, Sphecodina abbottii: False-eye and grape-patterns, found in Newton, MA on fox grape. William Hagar Ken Mallory George Mansfield y name is Sam Jaffe, and I founded bright warning colors, or strange inflatable Nyssa Patten The Caterpillar Lab — an tails and false eye-spots drew people in, Larry Smith Meducational outreach, art, and sparked interest and imagination. But today, Beth Wilkinson science non-profit organization that uses caterpillars represent so much more to native caterpillars and their stories to engage me. From working so closely with these Advisors and inspire the public with their own, local, insects for so long, from rearing over five Margaret Albright and ecologically important creatures. The hundred species and countless thousands of Lisle Baker Caterpillar Lab is a fluid thing, constantly individuals, and from bringing them to meet John Bliss changing as we learn from our audiences audiences every spring, summer, and fall, the Lee Breckenridge Lalor Burdick and our creatures alike. I would like to share world of caterpillars has exploded in size. -
Hawk Moths of North America Is Richly Illustrated with Larval Images and Contains an Abundance of Life History Information
08 caterpillars EUSA/pp244-273 3/9/05 6:37 PM Page 244 244 TULIP-TREE MOTH CECROPIA MOTH 245 Callosamia angulifera Hyalophora cecropia RECOGNITION Frosted green with shiny yellow, orange, and blue knobs over top and sides of body. RECOGNITION Much like preceding but paler or Dorsal knobs on T2, T3, and A1 somewhat globular and waxier in color with pale stripe running below set with black spinules. Paired knobs on A2–A7 more spiracles on A1–A10 and black dots on abdomen cylindrical, yellow; knob over A8 unpaired and rounded. lacking contrasting pale rings. Yellow abdominal Larva to 10cm. Caterpillars of larch-feeding Columbia tubercle over A8 short, less than twice as high as broad. Silkmoth (Hyalophora columbia) have yellow-white to Larva to 6cm. Sweetbay Silkmoth (Callosamia securifera) yellow-pink instead of bright yellow knobs over dorsum similar in appearance but a specialist on sweet bay. Its of abdomen and knobs along sides tend to be more white than blue (as in Cecropia) and are yellow abdominal tubercle over A8 is nearly three times as set in black bases (see page 246). long as wide and the red knobs over thorax are cylindrical (see page 246). OCCURRENCE Urban and suburban yards and lots, orchards, fencerows, woodlands, OCCURRENCE Woodlands and forests from Michigan, southern Ontario, and and forests from Canada south to Florida and central Texas. One generation with mature Massachusetts to northern Florida and Mississippi. One principal generation northward; caterpillars from late June through August over most of range. two broods in South with mature caterpillars from early June onward. -
Effect of Appendicularians and Copepods on Bacterioplankton Composition and Growth in the English Channel
AQUATIC MICROBIAL ECOLOGY Vol. 32: 39–46, 2003 Published May 12 Aquat Microb Ecol Effect of appendicularians and copepods on bacterioplankton composition and growth in the English Channel Mikhail V. Zubkov1,*, Angel López-Urrutia2 1George Deacon Division for Ocean Processes, Southampton Oceanography Centre, University of Southampton, Empress Dock, Southampton SO14 3ZH, United Kingdom 2Plymouth Marine Laboratory, Prospect Place, Plymouth PL1 3DH, United Kingdom ABSTRACT: We compared the effects of the presence of the appendicularian Oikopleura dioica and the copepods Acartia clausii and Calanus helgolandicus on the coastal bacterioplankton community off Plymouth. Mesozooplankton were added to water samples and bacterioplankton growth was monitored by flow cytometry. Phylogenetic composition of bacterioplankton was analysed using flu- orescence in situ hybridisation (FISH) with rRNA-targeted oligonucleotide probes. The bacterio- plankton composition did not change in the presence of either appendicularians or copepods, and generally the same proportions of bacterioplankton groups were determined. In late spring, 15 ± 2% of cells hybridised with a probe specific to the Kingdom Archaea. The majority of cells (88 ± 2%) belonged to the Kingdom Bacteria, and 86% of cells were identified using group-specific probes. The Cytophage-Flavobacterium cluster dominated the community, comprising 64 ± 0.5% of cells. The γ- proteobacteria were the second abundant group, comprising 11 ± 0.5% of cells, and the SAR86 clus- ter of γ-proteobacteria accounted for 6 ± 5%. The α-proteobacteria comprised 10 ± 5% of bacterio- plankton, and the Roseobacteria related cluster represented 9 ± 3% of cells. The reduction of bacterioplankton growth caused by appendicularian bacterivory was 0.4 to 14% ind.–1 l–1, and the total appendicularian population could reduce bacterial growth in coastal waters in late spring- summer by up to 9%. -
United States Department of the Interior
L/J'T United States Department of the Interior FISH AND WILDLIFE SERVICE PATUXENT WILDLIFE RESEARCH CENTER LAUREL, MARYLAND 20708 DEC 12 1986 Memorandum To: All Staff, Patuxent Wildlife Research Center (PWRC) Migratory Bird Management Office - Laurel (MBMO-L) From: Project Leader, Section of Planning and Development Subject: Species List Attached is a presence/absence species list for PWRC and vicinity prepared by the section of Planning and Development. This list was prepared by combining three species lists from: Committee of Biologists for Preservation of Natural Areas. 11 BP. ltsvi lle Federal Master Plan Area, Biological and Research Values and Recommendations for Land Use Master Planning. 11 Silver Spring, MD. Draft: Dec. 1976 Department of Army. 11 Draft Overall Installation Environmental Impact Statement, Existing Activities and Conditions. 11 The Environmental and Energy Control Office, Fort Geor9e Meade, MD, March 1979. Hotchkiss, Neil and Robert E. Stewart. Vegetation and Vertebrates of the Patuxent Wildlife Research Center: Laurel, MD, Original Edition, July 1947, Revised 1979. The list was developed for use in planning and for general reference in an 8 l / 2 x 11 format . Because we would like this list to be as up-to-date as possible, please review this draft and make any corrections or copies you think are necessary. We would like to finalize the draft and make it available for use by the end of January. Comments and corrections can be sent to the section of Planning and Development, attn: Kheryn. Thank yo help and expertise. Attachment PRELIMINARY SPECIES LIST PATUXENT WILDLIFE RESEARCH CENTER AND VICINITY CONTENTS Note Species Lists Vascular Plants Insects Butterflies and Moths Fishes Amphibians and Reptiles Birds Mammals References Note This presence/absence species list was assembled from three primary sources, listed at the end. -
Insects That Feed on Trees and Shrubs
INSECTS THAT FEED ON COLORADO TREES AND SHRUBS1 Whitney Cranshaw David Leatherman Boris Kondratieff Bulletin 506A TABLE OF CONTENTS DEFOLIATORS .................................................... 8 Leaf Feeding Caterpillars .............................................. 8 Cecropia Moth ................................................ 8 Polyphemus Moth ............................................. 9 Nevada Buck Moth ............................................. 9 Pandora Moth ............................................... 10 Io Moth .................................................... 10 Fall Webworm ............................................... 11 Tiger Moth ................................................. 12 American Dagger Moth ......................................... 13 Redhumped Caterpillar ......................................... 13 Achemon Sphinx ............................................. 14 Table 1. Common sphinx moths of Colorado .......................... 14 Douglas-fir Tussock Moth ....................................... 15 1. Whitney Cranshaw, Colorado State University Cooperative Extension etnomologist and associate professor, entomology; David Leatherman, entomologist, Colorado State Forest Service; Boris Kondratieff, associate professor, entomology. 8/93. ©Colorado State University Cooperative Extension. 1994. For more information, contact your county Cooperative Extension office. Issued in furtherance of Cooperative Extension work, Acts of May 8 and June 30, 1914, in cooperation with the U.S. Department of Agriculture, -
(12) Patent Application Publication (10) Pub. No.: US 2009/0099135A1 Enan (43) Pub
US 20090099.135A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2009/0099135A1 Enan (43) Pub. Date: Apr. 16, 2009 (54) PEST CONTROL COMPOSITIONS AND Publication Classification METHODS (51) Int. Cl. AOIN 57/6 (2006.01) AOIN 47/2 (2006.01) (75) Inventor: Essam Enan, Davis, CA (US) AOIN 43/12 (2006.01) AOIN 57/4 (2006.01) AOIN 53/06 (2006.01) Correspondence Address: AOIN 5L/00 (2006.01) SONNENSCHEN NATH & ROSENTHAL LLP AOIN 43/40 (2006.01) AOIP3/00 (2006.01) P.O. BOX 061080, WACKER DRIVE STATION, AOIP 7/04 (2006.01) SEARS TOWER AOIP 7/02 (2006.01) CHICAGO, IL 60606-1080 (US) AOIN 43/90 (2006.01) AOIN 43/6 (2006.01) AOIN 43/56 (2006.01) (73) Assignee: TyraTech, Inc., Melbourne, FL AOIN 29/2 (2006.01) (US) AOIN 43/52 (2006.01) AOIN 57/12 (2006.01) (52) U.S. Cl. ........... 514/86; 514/477; 514/469; 514/481; (21) Appl. No.: 12/009,220 514/395; 514/122:514/89: 514/486; 514/132: 514/748; 514/520; 514/531; 514/.407: 514/365; 514/341; 514/453: 514/343; 514/299 (22) Filed: Jan. 16, 2008 (57) ABSTRACT Embodiments of the present invention provide compositions for controlling a target pest including a pest control product Related U.S. Application Data and at least one active agent, wherein: the active agent can be capable of interacting with a receptor in the target pest; the (60) Provisional application No. 60/885,214, filed on Jan. pest control product can have a first activity against the target 16, 2007, provisional application No. -
National Monitoring Program for Biodiversity and Non-Indigenous Species in Egypt
National monitoring program for biodiversity and non-indigenous species in Egypt January 2016 1 TABLE OF CONTENTS page Acknowledgements 3 Preamble 4 Chapter 1: Introduction 8 Overview of Egypt Biodiversity 37 Chapter 2: Institutional and regulatory aspects 39 National Legislations 39 Regional and International conventions and agreements 46 Chapter 3: Scientific Aspects 48 Summary of Egyptian Marine Biodiversity Knowledge 48 The Current Situation in Egypt 56 Present state of Biodiversity knowledge 57 Chapter 4: Development of monitoring program 58 Introduction 58 Conclusions 103 Suggested Monitoring Program Suggested monitoring program for habitat mapping 104 Suggested marine MAMMALS monitoring program 109 Suggested Marine Turtles Monitoring Program 115 Suggested Monitoring Program for Seabirds 117 Suggested Non-Indigenous Species Monitoring Program 121 Chapter 5: Implementation / Operational Plan 128 Selected References 130 Annexes 141 2 AKNOWLEGEMENTS 3 Preamble The Ecosystem Approach (EcAp) is a strategy for the integrated management of land, water and living resources that promotes conservation and sustainable use in an equitable way, as stated by the Convention of Biological Diversity. This process aims to achieve the Good Environmental Status (GES) through the elaborated 11 Ecological Objectives and their respective common indicators. Since 2008, Contracting Parties to the Barcelona Convention have adopted the EcAp and agreed on a roadmap for its implementation. First phases of the EcAp process led to the accomplishment of 5 steps of the scheduled 7-steps process such as: 1) Definition of an Ecological Vision for the Mediterranean; 2) Setting common Mediterranean strategic goals; 3) Identification of an important ecosystem properties and assessment of ecological status and pressures; 4) Development of a set of ecological objectives corresponding to the Vision and strategic goals; and 5) Derivation of operational objectives with indicators and target levels.