Biology 2 Animal Diversity
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Eriocheir Sinensis Potential in RI COASTAL WATERS Chinese Mitten Crab Invader
GUIDE TO MARINE INVADERS Eriocheir sinensis Potential IN RI COASTAL WATERS Chinese mitten crab Invader PHYSICAL DESCRIPTION • Dense fuzzy patches on claws of adults and larger juveniles (>1 inch) • Regenerated claws and claws of smaller juveniles may not have fuzz • Claws are equally sized and white-tipped • Four lateral spines on each side of carapace (shell); notch between the eyes • Carapace light-brown to olive green color; width up to 4 in (10 cm) • Sharp-tipped walking legs of adult over twice as long as carapace width Lee Mecum, CDF&G notch Adult Eriocheir sinensis fuzzy claws with HABITAT PREFERENCE white pincers • Catadromous life cycle: begins as estuarine larva, migrates into freshwater streams for 1-4 years, then returns to coast to reproduce 4 lateral • Burrows in the bottom and banks of freshwater rivers and estuaries spines • Tolerates a wide range of temperatures • Able to survive in highly altered and polluted aquatic habitats • Adept at walking on land and around barriers • Nondiscriminating omnivores that consume plants and prey on fish and benthic invertebrates (clams, worms, shrimp) 1 2 3 4 5 6 © Rob Gough, DFBW 7 8 GUIDE TO MARINE INVADERS Eriocheir sinensis Potential IN RI COASTAL WATERS Chinese mitten crab Invader INVASION STATUS & ECOLOGICAL CONCERNS Native to east Asia, Eriocheir sinensis has achieved a global distribution that includes several countries in central and western Europe and most recently the U.S. Pacific and Atlantic coasts. In 1992, it was found reproducing in San Francisco Bay. By 1998, E.sinensis had spread throughout the bay and has since expanded upstream into the Sacramento and San Joaquin Rivers. -
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. -
Eriocheir Sinensis Potential in the GULF of MAINE Chinese Mitten Crab Invader
GUIDE TO MARINE INVADERS Eriocheir sinensis Potential IN THE GULF OF MAINE Chinese mitten crab Invader PHYSICAL DESCRIPTION • Dense fuzzy patches on claws of adults and larger juveniles (>1 inch) • Regenerated claws and claws of smaller juveniles may not have fuzz • Claws are equally sized and white-tipped • Four lateral spines on each side of carapace (shell); notch between the eyes • Carapace light-brown to olive green color; width up to 4 in (10 cm) • Sharp-tipped walking legs of adult over twice as long as carapace width Lee Mecum, CDF&G notch Adult Eriocheir sinensis fuzzy claws with HABITAT PREFERENCE white pincers • Catadromous life cycle: begins as estuarine larva, migrates into freshwater streams for 1-4 years, then returns to coast to reproduce 4 lateral • Burrows in the bottom and banks of freshwater rivers and estuaries spines • Tolerates a wide range of temperatures • Able to survive in highly altered and polluted aquatic habitats • Adept at walking on land and around barriers • Nondiscriminating omnivores that consume plants and prey on fish and benthic invertebrates (clams, worms, shrimp) Rob Gough 1 2 3 4 5 6 7 8 GUIDE TO MARINE INVADERS Eriocheir sinensis Potential IN THE GULF OF MAINE Chinese mitten crab Invader INVASION STATUS & ECOLOGICAL CONCERNS Native to east Asia, Eriocheir sinensis has achieved a global distribution that includes several countries in central and western Europe and most recently the U.S. Pacific and Atlantic coasts. In 1992, it was found reproducing in San Francisco Bay. By 1998, E.sinensis had spread throughout the bay and has since expanded upstream into the Sacramento and San Joaquin Rivers. -
Atlanta Ariejansseni, a New Species of Shelled Heteropod from the Southern Subtropical Convergence Zone (Gastropoda, Pterotracheoidea)
A peer-reviewed open-access journal ZooKeys 604: 13–30 (2016) Atlanta ariejansseni, a new species of shelled heteropod.... 13 doi: 10.3897/zookeys.604.8976 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Atlanta ariejansseni, a new species of shelled heteropod from the Southern Subtropical Convergence Zone (Gastropoda, Pterotracheoidea) Deborah Wall-Palmer1,2, Alice K. Burridge2,3, Katja T.C.A. Peijnenburg2,3 1 School of Geography, Earth and Environmental Sciences, Plymouth University, Drake Circus, Plymouth, PL4 8AA, UK 2 Naturalis Biodiversity Center, Darwinweg 2, 2333 CR Leiden, The Netherlands3 Institute for Biodiversity and Ecosystem Dynamics (IBED), University of Amsterdam, P. O. Box 94248, 1090 GE Amster- dam, The Netherlands Corresponding author: Deborah Wall-Palmer ([email protected]) Academic editor: N. Yonow | Received 21 April 2016 | Accepted 22 June 2016 | Published 11 July 2016 http://zoobank.org/09E534C5-589D-409E-836B-CF64A069939D Citation: Wall-Palmer D, Burridge AK, Peijnenburg KTCA (2016) Atlanta ariejansseni, a new species of shelled heteropod from the Southern Subtropical Convergence Zone (Gastropoda, Pterotracheoidea). ZooKeys 604: 13–30. doi: 10.3897/zookeys.604.8976 Abstract The Atlantidae (shelled heteropods) is a family of microscopic aragonite shelled holoplanktonic gastro- pods with a wide biogeographical distribution in tropical, sub-tropical and temperate waters. The arago- nite shell and surface ocean habitat of the atlantids makes them particularly susceptible to ocean acidifica- tion and ocean warming, and atlantids are likely to be useful indicators of these changes. However, we still lack fundamental information on their taxonomy and biogeography, which is essential for monitoring the effects of a changing ocean. -
Number of Living Species in Australia and the World
Numbers of Living Species in Australia and the World 2nd edition Arthur D. Chapman Australian Biodiversity Information Services australia’s nature Toowoomba, Australia there is more still to be discovered… Report for the Australian Biological Resources Study Canberra, Australia September 2009 CONTENTS Foreword 1 Insecta (insects) 23 Plants 43 Viruses 59 Arachnida Magnoliophyta (flowering plants) 43 Protoctista (mainly Introduction 2 (spiders, scorpions, etc) 26 Gymnosperms (Coniferophyta, Protozoa—others included Executive Summary 6 Pycnogonida (sea spiders) 28 Cycadophyta, Gnetophyta under fungi, algae, Myriapoda and Ginkgophyta) 45 Chromista, etc) 60 Detailed discussion by Group 12 (millipedes, centipedes) 29 Ferns and Allies 46 Chordates 13 Acknowledgements 63 Crustacea (crabs, lobsters, etc) 31 Bryophyta Mammalia (mammals) 13 Onychophora (velvet worms) 32 (mosses, liverworts, hornworts) 47 References 66 Aves (birds) 14 Hexapoda (proturans, springtails) 33 Plant Algae (including green Reptilia (reptiles) 15 Mollusca (molluscs, shellfish) 34 algae, red algae, glaucophytes) 49 Amphibia (frogs, etc) 16 Annelida (segmented worms) 35 Fungi 51 Pisces (fishes including Nematoda Fungi (excluding taxa Chondrichthyes and (nematodes, roundworms) 36 treated under Chromista Osteichthyes) 17 and Protoctista) 51 Acanthocephala Agnatha (hagfish, (thorny-headed worms) 37 Lichen-forming fungi 53 lampreys, slime eels) 18 Platyhelminthes (flat worms) 38 Others 54 Cephalochordata (lancelets) 19 Cnidaria (jellyfish, Prokaryota (Bacteria Tunicata or Urochordata sea anenomes, corals) 39 [Monera] of previous report) 54 (sea squirts, doliolids, salps) 20 Porifera (sponges) 40 Cyanophyta (Cyanobacteria) 55 Invertebrates 21 Other Invertebrates 41 Chromista (including some Hemichordata (hemichordates) 21 species previously included Echinodermata (starfish, under either algae or fungi) 56 sea cucumbers, etc) 22 FOREWORD In Australia and around the world, biodiversity is under huge Harnessing core science and knowledge bases, like and growing pressure. -
Studying an Elusive Cuckoo Sarah C
INNER WORKINGS INNER WORKINGS Studying an elusive cuckoo Sarah C. P. Williams fi Science Writer a eld site in Panama operated by the Smithsonian Tropical Research Institute. “They only build nests overhanging water and so you need to boat—often through In a single nest, perched on a branch over- A dozen feet away, researchers peer out of waters with lots of crocodiles—to see the hanging a marshy river in Panama, four birds an idling boat, binoculars to their faces as nests or catch the birds for banding and jostle for space. The birds all belong to a they count the birds, the eggs, and note the blood samples.” species of cuckoo called the Greater Ani, and colors of the bands clamped around each However, the communal nesting habits of each one has offspring in the communal nest. bird’sleg. the Greater Ani has Riehl intrigued. She’s The birds take turns warming the heap of eggs “The Anis are really hard to study,” says spent the past five years tracking birds, in- and looking out for predators, teaming to- Christina Riehl, a junior fellow with the stalling video cameras above their nests, and gether to face the challenges of rearing young. Harvard Society of Fellows, who works at studying the genetics of each generation of birds to understand their behaviors. TheAnisnestingroupsoftwotofour male-femalepairs,addinguptofourtoeight adults per nest. Riehl has discovered that the bigger the group, the more young that survive, suggesting a clear advantage to the cooperation. However, there’s competition in the mix too; before a female lays her own eggs, she’ll try to kick other females’ eggs out of the nest. -
“Italian Immigrants” Flourish on Long Island Russell Burke Associate Professor Department of Biology
“Italian Immigrants” Flourish on Long Island Russell Burke Associate Professor Department of Biology talians have made many important brought ringneck pheasants (Phasianus mentioned by Shakespeare. Also in the contributions to the culture and colchicus) to North America for sport late 1800s naturalists introduced the accomplishments of the United hunting, and pheasants have survived so small Indian mongoose (Herpestes javan- States, and some of these are not gen- well (for example, on Hofstra’s North icus) to the islands of Mauritius, Fiji, erally appreciated. Two of the more Campus) that many people are unaware Hawai’i, and much of the West Indies, Iunderappreciated contributions are that the species originated in China. Of supposedly to control the rat popula- the Italian wall lizards, Podarcis sicula course most of our common agricultural tion. Rats were crop pests, and in most and Podarcis muralis. In the 1960s and species — except for corn, pumpkins, cases the rats were introduced from 1970s, Italian wall lizards were imported and some beans — are non-native. The Europe. Instead of eating lots of rats, the to the United States in large numbers for mongooses ate numerous native ani- the pet trade. These hardy, colorful little mals, endangering many species and lizards are common in their home coun- Annual Patterns causing plenty of extinctions. They also try, and are easily captured in large num- 3.0 90 became carriers of rabies. There are 80 2.5 bers. Enterprising animal dealers bought 70 many more cases of introductions like them at a cut rate in Italy and sold them 2.0 60 these, and at the time the scientific 50 1.5 to pet dealers all over the United States. -
Animal Phylum Poster Porifera
Phylum PORIFERA CNIDARIA PLATYHELMINTHES ANNELIDA MOLLUSCA ECHINODERMATA ARTHROPODA CHORDATA Hexactinellida -- glass (siliceous) Anthozoa -- corals and sea Turbellaria -- free-living or symbiotic Polychaetes -- segmented Gastopods -- snails and slugs Asteroidea -- starfish Trilobitomorpha -- tribolites (extinct) Urochordata -- tunicates Groups sponges anemones flatworms (Dugusia) bristleworms Bivalves -- clams, scallops, mussels Echinoidea -- sea urchins, sand Chelicerata Cephalochordata -- lancelets (organisms studied in detail in Demospongia -- spongin or Hydrazoa -- hydras, some corals Trematoda -- flukes (parasitic) Oligochaetes -- earthworms (Lumbricus) Cephalopods -- squid, octopus, dollars Arachnida -- spiders, scorpions Mixini -- hagfish siliceous sponges Xiphosura -- horseshoe crabs Bio1AL are underlined) Cubozoa -- box jellyfish, sea wasps Cestoda -- tapeworms (parasitic) Hirudinea -- leeches nautilus Holothuroidea -- sea cucumbers Petromyzontida -- lamprey Mandibulata Calcarea -- calcareous sponges Scyphozoa -- jellyfish, sea nettles Monogenea -- parasitic flatworms Polyplacophora -- chitons Ophiuroidea -- brittle stars Chondrichtyes -- sharks, skates Crustacea -- crustaceans (shrimp, crayfish Scleropongiae -- coralline or Crinoidea -- sea lily, feather stars Actinipterygia -- ray-finned fish tropical reef sponges Hexapoda -- insects (cockroach, fruit fly) Sarcopterygia -- lobed-finned fish Myriapoda Amphibia (frog, newt) Chilopoda -- centipedes Diplopoda -- millipedes Reptilia (snake, turtle) Aves (chicken, hummingbird) Mammalia -
Protein and Lipid Characterization of Acheta Domesticus, Bombyx Mori, and Locusta Migratoria Dry Flours
Graduate Theses, Dissertations, and Problem Reports 2018 Protein and Lipid Characterization of Acheta domesticus, Bombyx mori, and Locusta migratoria Dry Flours Emily N. Brogan Follow this and additional works at: https://researchrepository.wvu.edu/etd Part of the Food Chemistry Commons, and the Food Microbiology Commons Recommended Citation Brogan, Emily N., "Protein and Lipid Characterization of Acheta domesticus, Bombyx mori, and Locusta migratoria Dry Flours" (2018). Graduate Theses, Dissertations, and Problem Reports. 7498. https://researchrepository.wvu.edu/etd/7498 This Thesis is protected by copyright and/or related rights. It has been brought to you by the The Research Repository @ WVU with permission from the rights-holder(s). You are free to use this Thesis in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you must obtain permission from the rights-holder(s) directly, unless additional rights are indicated by a Creative Commons license in the record and/ or on the work itself. This Thesis has been accepted for inclusion in WVU Graduate Theses, Dissertations, and Problem Reports collection by an authorized administrator of The Research Repository @ WVU. For more information, please contact [email protected]. Protein and Lipid Characterization of Acheta domesticus, Bombyx mori, and Locusta migratoria Dry Flours Emily N. Brogan Thesis submitted to the Davis College of Agriculture, Natural Resources and Design at West Virginia University in partial fulfilment of the requirements for the degree of Master of Science in Nutritional and Food Science Jacek Jaczynski Ph.D., chair Kristen Matak Ph. D Yong-Lak Park, Ph. -
Feeding Habits of an Exotic Species, the Mediterranean Green Crab Carcinus Aestuarii, in Tokyo Bay
Feeding habits of Car cinus aestuarii RB Chen et al. 10.1046/j.1444-2906.2004.00822.x Original Article430435BEES SGML FISHERIES SCIENCE 2004; 70: 430–435 Feeding habits of an exotic species, the Mediterranean green crab Carcinus aestuarii, in Tokyo Bay Rong Bin CHEN, Seiichi WATANABE* AND Masashi YOKOTA Department of Aquatic Biosciences, Tokyo University of Marine Science and Technology, Minato, Tokyo 108-8477, Japan ABSTRACT: Feeding habits of an exotic species, the Mediterranean green crab Carcinus aestuarii, in Tokyo Bay, Japan, were studied based on the analysis of stomach contents. Monthly samples were taken from May 2000 to October 2001 at stations near the Keihin Canal along the northern shore of Tokyo Bay. Stomach contents of 367 crabs (male n = 200, female n = 167) were examined. Carapace width ranged from 18.50 mm to 60.67 mm. Eleven food categories were identified: Bivalvia (mostly Mytilus galloprovincialis), other Mollusca, Cirripedia, Amphipoda, Brachyura, other Crustacea, Poly- chaeta, Pisces, unidentified animal materials, plant materials, and unidentified materials. The results showed that C. aestuarii is an omnivorous predator and that its diet depends greatly upon the availability of local prey species, especially in intertidal areas. Moreover, the analysis found no significant differences in the feeding habits of crabs of different sizes or sexes. KEY WORDS: Carcinus aestuarii, exotic species, feeding habits, stomach contents, Tokyo Bay. INTRODUCTION that they were scavengers and predators. The bulk of their prey consisted of slow-moving and sessile Many exotic species have established natural invertebrates, with algae comprising only a small populations in Japan in recent years. -
Species Composition and Invasion Risks of Alien Ornamental Freshwater
www.nature.com/scientificreports OPEN Species composition and invasion risks of alien ornamental freshwater fshes from pet stores in Klang Valley, Malaysia Abdulwakil Olawale Saba1,2, Ahmad Ismail1, Syaizwan Zahmir Zulkifi1, Muhammad Rasul Abdullah Halim3, Noor Azrizal Abdul Wahid4 & Mohammad Noor Azmai Amal1* The ornamental fsh trade has been considered as one of the most important routes of invasive alien fsh introduction into native freshwater ecosystems. Therefore, the species composition and invasion risks of fsh species from 60 freshwater fsh pet stores in Klang Valley, Malaysia were studied. A checklist of taxa belonging to 18 orders, 53 families, and 251 species of alien fshes was documented. Fish Invasiveness Screening Test (FIST) showed that seven (30.43%), eight (34.78%) and eight (34.78%) species were considered to be high, medium and low invasion risks, respectively. After the calibration of the Fish Invasiveness Screening Kit (FISK) v2 using the Receiver Operating Characteristics, a threshold value of 17 for distinguishing between invasive and non-invasive fshes was identifed. As a result, nine species (39.13%) were of high invasion risk. In this study, we found that non-native fshes dominated (85.66%) the freshwater ornamental trade in Klang Valley, while FISK is a more robust tool in assessing the risk of invasion, and for the most part, its outcome was commensurate with FIST. This study, for the frst time, revealed the number of high-risk ornamental fsh species that give an awareness of possible future invasion if unmonitored in Klang Valley, Malaysia. As a global hobby, fshkeeping is cherished by both young and old people. -
Reactivating the Lake Junín Giant Frog Monitoring Program
December 2020 AMPHIBIAN SURVIVAL ALLIANCE NEWTSLETTER Got a story you want to share? Drop Candace an email today! [email protected] Stories from our partners around the world © Rogger Angel Moreno Lino Moreno Angel © Rogger Reactivating the Lake Junín Giant Frog monitoring program By Rogger Angel Moreno Lino, Luis and economy; businesses and NGOs In this way, ASA partner Grupo Castillo Roque and Roberto Elias have stopped their activities and RANA participated in a project for Piperis. Grupo RANA (Peru) and reduced their budgets among other the monitoring and surveillance of Denver Zoological Foundation (U.S.) things (Smith-Bingham & Harlharan, populations of the Lake Junín Giant [email protected] 2020; Crothers, 2020). However, Frog (Telmatobius macrostomus) solidarity among people and institu- and the Junín ‘Wanchas’ (Telma- The world is going through difficult tions has allowed activities to be tobius brachydactylus) in three times due to the COVID-19 pan- progressively reactivated, though protected natural areas (Junín Na- demic (WWF, 2020). Many people following rigorous biosecurity meas- tional Reserve, Historic Sanctuary of have been affected in their health ures. Chacamarca and Huayllay National Page 1 Sanctuary). These activities were by Pablo Miñano Lecaros. The park (CCPH), the presence of six adult led by the Denver Zoological Foun- rangers Winy Arias López, Eduardo frogs was recorded around 500 dation and funded by the National Ruiz and Duane Martínez supported meters from our monitoring point Geographic Society and followed the the activities. at the south of the Junín National biosecurity measures recommended As part of the preliminary results, Reserve. by the Ministry of Health of Peru we report three adults of the Junín It should be noted that the CCPH (D.S.