Razor Clam Final Report 2005
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American Oystercatcher
Maine 2015 Wildlife Action Plan Revision Report Date: January 13, 2016 Haematopus palliatus (American Oystercatcher) Priority 3 Species of Greatest Conservation Need (SGCN) Class: Aves (Birds) Order: Charadriiformes (Plovers, Sandpipers, And Allies) Family: Haematopodidae (Oystercatchers) General comments: First nesting record in Maine - 1994. 4 - 8 breeding pairs in Maine, range expansion, Northern Atlantic population 11,000 and considered stable. Listed as Critical risk category because of high vulnerability to climate change - Gilbrathe et al. 2014. Species Conservation Range Maps for American Oystercatcher: Town Map: Haematopus palliatus_Towns.pdf Subwatershed Map: Haematopus palliatus_HUC12.pdf SGCN Priority Ranking - Designation Criteria: Risk of Extirpation: NA State Special Concern or NMFS Species of Concern: Haematopus palliatus is listed as a species of Special Concern in Maine. Recent Significant Declines: NA Regional Endemic: NA High Regional Conservation Priority: United States Shorebird Conservation Plan: Species of High Concern North Atlantic Regional Shorebird Plan: Highly Imperiled United States Birds of Conservation Concern: Bird of Conservation Concern in Bird Conservation Regions 14 and/or 30: Yes High Climate Change Vulnerability: Vulnerability: 3, Confidence: High, Reviewers: Decided in Workshop (W) Understudied rare taxa: NA Historical: NA Culturally Significant: NA Habitats Assigned to American Oystercatcher: Formation Name Cliff & Rock Macrogroup Name Rocky Coast Formation Name Intertidal Macrogroup Name Intertidal -
List of Shorebird Profiles
List of Shorebird Profiles Pacific Central Atlantic Species Page Flyway Flyway Flyway American Oystercatcher (Haematopus palliatus) •513 American Avocet (Recurvirostra americana) •••499 Black-bellied Plover (Pluvialis squatarola) •488 Black-necked Stilt (Himantopus mexicanus) •••501 Black Oystercatcher (Haematopus bachmani)•490 Buff-breasted Sandpiper (Tryngites subruficollis) •511 Dowitcher (Limnodromus spp.)•••485 Dunlin (Calidris alpina)•••483 Hudsonian Godwit (Limosa haemestica)••475 Killdeer (Charadrius vociferus)•••492 Long-billed Curlew (Numenius americanus) ••503 Marbled Godwit (Limosa fedoa)••505 Pacific Golden-Plover (Pluvialis fulva) •497 Red Knot (Calidris canutus rufa)••473 Ruddy Turnstone (Arenaria interpres)•••479 Sanderling (Calidris alba)•••477 Snowy Plover (Charadrius alexandrinus)••494 Spotted Sandpiper (Actitis macularia)•••507 Upland Sandpiper (Bartramia longicauda)•509 Western Sandpiper (Calidris mauri) •••481 Wilson’s Phalarope (Phalaropus tricolor) ••515 All illustrations in these profiles are copyrighted © George C. West, and used with permission. To view his work go to http://www.birchwoodstudio.com. S H O R E B I R D S M 472 I Explore the World with Shorebirds! S A T R ER G S RO CHOOLS P Red Knot (Calidris canutus) Description The Red Knot is a chunky, medium sized shorebird that measures about 10 inches from bill to tail. When in its breeding plumage, the edges of its head and the underside of its neck and belly are orangish. The bird’s upper body is streaked a dark brown. It has a brownish gray tail and yellow green legs and feet. In the winter, the Red Knot carries a plain, grayish plumage that has very few distinctive features. Call Its call is a low, two-note whistle that sometimes includes a churring “knot” sound that is what inspired its name. -
Siliqua Patula Class: Bivalvia; Heterodonta Order: Veneroida the Flat Razor Clam Family: Pharidae
Phylum: Mollusca Siliqua patula Class: Bivalvia; Heterodonta Order: Veneroida The flat razor clam Family: Pharidae Taxonomy: The familial designation of this (see Plate 397G, Coan and Valentich-Scott species has changed frequently over time. 2007). Previously in the Solenidae, current intertidal Body: (see Plate 29 Ricketts and Calvin guides include S. patula in the Pharidae (e.g., 1952; Fig 259 Kozloff 1993). Coan and Valentich-Scott 2007). The superfamily Solenacea includes infaunal soft Color: bottom dwelling bivalves and contains the two Interior: (see Fig 5, Pohlo 1963). families: Solenidae and Pharidae (= Exterior: Cultellidae, von Cosel 1993) (Remacha- Byssus: Trivino and Anadon 2006). In 1788, Dixon Gills: described S. patula from specimens collected Shell: The shell in S. patula is thin and with in Alaska (see Range) and Conrad described sharp (i.e., razor-like) edges and a thin profile the same species, under the name Solen (Fig. 4). Thin, long, fragile shell (Ricketts and nuttallii from specimens collected in the Calvin 1952), with gapes at both ends Columbia River in 1838 (Weymouth et al. (Haderlie and Abbott 1980). Shell smooth 1926). These names were later inside and out (Dixon 1789), elongate, rather synonymized, thus known synonyms for cylindrical and the length is about 2.5 times Siliqua patula include Solen nuttallii, the width. Solecurtus nuttallii. Occasionally, researchers Interior: Prominent internal vertical also indicate a subspecific epithet (e.g., rib extending from beak to margin (Haderlie Siliqua siliqua patula) or variations (e.g., and Abbott 1980). Siliqua patula var. nuttallii, based on rib Exterior: Both valves are similar and morphology, see Possible gape at both ends. -
Embryonic and Larval Development of Ensis Arcuatus (Jeffreys, 1865) (Bivalvia: Pharidae)
EMBRYONIC AND LARVAL DEVELOPMENT OF ENSIS ARCUATUS (JEFFREYS, 1865) (BIVALVIA: PHARIDAE) FIZ DA COSTA, SUSANA DARRIBA AND DOROTEA MARTI´NEZ-PATIN˜O Centro de Investigacio´ns Marin˜as, Consellerı´a de Pesca e Asuntos Marı´timos, Xunta de Galicia, Apdo. 94, 27700 Ribadeo, Lugo, Spain (Received 5 December 2006; accepted 19 November 2007) ABSTRACT The razor clam Ensis arcuatus (Jeffreys, 1865) is distributed from Norway to Spain and along the British coast, where it lives buried in sand in low intertidal and subtidal areas. This work is the first study to research the embryology and larval development of this species of razor clam, using light and scanning electron microscopy. A new method, consisting of changing water levels using tide simulations with brief Downloaded from https://academic.oup.com/mollus/article/74/2/103/1161011 by guest on 23 September 2021 dry periods, was developed to induce spawning in this species. The blastula was the first motile stage and in the gastrula stage the vitelline coat was lost. The shell field appeared in the late gastrula. The trocho- phore developed by about 19 h post-fertilization (hpf) (198C). At 30 hpf the D-shaped larva showed a developed digestive system consisting of a mouth, a foregut, a digestive gland followed by an intestine and an anus. Larvae spontaneously settled after 20 days at a length of 378 mm. INTRODUCTION following families: Mytilidae (Redfearn, Chanley & Chanley, 1986; Fuller & Lutz, 1989; Bellolio, Toledo & Dupre´, 1996; Ensis arcuatus (Jeffreys, 1865) is the most abundant species of Hanyu et al., 2001), Ostreidae (Le Pennec & Coatanea, 1985; Pharidae in Spain. -
Business Plan for the Conservation of the American Oystercatcher
Business Plan for the Conservation of the American Oystercatcher A 10-Year Plan to Secure a Coastal Keystone Species American Oystercatcher Working Group National Fish and Wildlife Foundation October 26, 2008 i WHAT IS A BUSINESS PLAN? A business plan serves two broad, primary functions. First, it provides specific information to those (e.g., prospective investors) not familiar with the proposed or existing business, including its goals and the management strategy and financial and other resources necessary to attain those goals. For outside individuals, it is imperative that the business plan offer a clear rationale for why the goals represent a good investment and why the strategy for achieving those goals is the best one possible. Second, a business plan provides internal guidance to those who are active in the operation of the business, allowing all individuals to understand where the business is headed and the means by which it will get there. The plan helps keep the business from drifting away from its goals and key actions through careful articulation of a strategy. In the context of the National Fish and Wildlife Foundation’s conservation efforts, business plans represent the strategies necessary to meet the goals of Keystone and other initiatives. At its core, each business plan emphasizes the type(s) and magnitude of the impacts (benefits) that will be realized through the initiative, the monetary costs involved, and the potential obstacles (risks) to achieving those gains. Readers of the business plan must be able to see the strength of the relationship between the activities identified within the strategy and the anticipated outcomes. -
IDENTIFYING HYBRID OYSTERCATCHERS in SOUTHERN CALIFORNIA WALTER WEHTJE, 2286 Barbara Drive, Camarillo, California 93012; [email protected]
FEATURED PHOTO IDENTIFYING HYBRID OYSTERCATCHERS IN SOUTHERN CALIFORNIA WALTER WEHTJE, 2286 Barbara Drive, Camarillo, California 93012; [email protected] The photo featured on the back cover of this issue was taken on 26 May 2005 on the south side of San Nicolas Island, Ventura County, California. Its subject appears to be a rather dark American Oystercatcher (Haematopus palliatus). A large shorebird of sandy beaches, tidal mudflats and rocky shores, along the Pacific coast this species ranges from central Chile to central Baja California. In central Baja California it is replaced by the Black Oystercatcher (H. bachmani), a bird of rocky shorelines that ranges north to the Aleutian Islands. For a 300-mile stretch along the Baja California peninsula the two species interbreed, forming a stable hybrid zone (Jehl 1985). Any pied oystercatcher observed north of the international border had probably wandered north from Baja California and has to be examined closely. Of the 35 documented sightings of “American” Oystercatchers in southern California, 11 have proved to be of hybrids (Cole and McCaskie 2004). So what constitutes a “good” American Oystercatcher? Jehl posed this question more than 20 years ago. Using techniques developed for studying hybrid popula- tions devised by Charles Sibley and his students (e.g., Sibley and Short 1959), Jehl established a hybrid index for black and pied oystercatchers. Specifically, he scored the uppertail coverts, tail, chest, undertail coverts, thighs, greater secondary coverts, extent of white wing stripe, underwing coverts, and axillaries from 0 (black, as in H. bachmani) to 4 (white, as in H. palliatus). The character score for the belly ranged from 0 to 6. -
An Annotated Checklist of the Marine Macroinvertebrates of Alaska David T
NOAA Professional Paper NMFS 19 An annotated checklist of the marine macroinvertebrates of Alaska David T. Drumm • Katherine P. Maslenikov Robert Van Syoc • James W. Orr • Robert R. Lauth Duane E. Stevenson • Theodore W. Pietsch November 2016 U.S. Department of Commerce NOAA Professional Penny Pritzker Secretary of Commerce National Oceanic Papers NMFS and Atmospheric Administration Kathryn D. Sullivan Scientific Editor* Administrator Richard Langton National Marine National Marine Fisheries Service Fisheries Service Northeast Fisheries Science Center Maine Field Station Eileen Sobeck 17 Godfrey Drive, Suite 1 Assistant Administrator Orono, Maine 04473 for Fisheries Associate Editor Kathryn Dennis National Marine Fisheries Service Office of Science and Technology Economics and Social Analysis Division 1845 Wasp Blvd., Bldg. 178 Honolulu, Hawaii 96818 Managing Editor Shelley Arenas National Marine Fisheries Service Scientific Publications Office 7600 Sand Point Way NE Seattle, Washington 98115 Editorial Committee Ann C. Matarese National Marine Fisheries Service James W. Orr National Marine Fisheries Service The NOAA Professional Paper NMFS (ISSN 1931-4590) series is pub- lished by the Scientific Publications Of- *Bruce Mundy (PIFSC) was Scientific Editor during the fice, National Marine Fisheries Service, scientific editing and preparation of this report. NOAA, 7600 Sand Point Way NE, Seattle, WA 98115. The Secretary of Commerce has The NOAA Professional Paper NMFS series carries peer-reviewed, lengthy original determined that the publication of research reports, taxonomic keys, species synopses, flora and fauna studies, and data- this series is necessary in the transac- intensive reports on investigations in fishery science, engineering, and economics. tion of the public business required by law of this Department. -
The Factors Affecting Productivity and Parental
THE FACTORS AFFECTING PRODUCTIVITY AND PARENTAL BEHAVIOR OF AMERICAN OYSTERCATCHERS IN TEXAS by Amanda N. Anderson, B.S. THESIS Presented to the faculty of The University of Houston-Clear Lake in partial fulfillment of the requirements for the degree MASTERS OF SCIENCE THE UNIVERSITY OF HOUSTON CLEAR LAKE December, 2014 ACKNOWLEDGEMENTS I would first like to give thanks and love to my parents, Lisa and Eddie for their ongoing support. You have been my rock in all circumstances and helped me persevere through life’s obstacles. I would not be the independent, hard-working, or accomplished woman I am today without you two. I want to recognize my brother, grandparents, and extended family. I have always cherished our time together during my visits back home. Thanks to my significant other, Sean Stewart for helping me get through these last few months. To my advisor, George Guillen, thank you for your guidance, support, and the opportunity to work on an amazing project. My intention for completing a research thesis was to intimately study waterbirds, and you helped me do so. I would also like to thank Jenny Oakley for providing logistical support. To my mentor and sidekick, Susan Heath, I am immensely grateful for your support, advice, and patience over the last two years. You taught me so much and helped me along the path to my avian career. I admire your passion for birds and hope I’m as bad ass as you are when I’m fifty something! I would like to thank Felipe Chavez for his ornithological expertise and always helping when called upon. -
A Global Assessment of the Conservation Status of the Black Oystercatcher Haematopus Bachmani
A global assessment of the conservation status of the Black Oystercatcher Haematopus bachmani David F. Tessle r1, James A. Johnso n2, Brad A. Andres 3, Sue Thoma s4 & Richard B. Lancto t2 1Alaska Department of Fish and Game, Division of Wildlife Conservation, Wildlife Diversity Program, 333 Raspberry Road, Anchorage, Alaska 99518 USA. [email protected] 2United States Fish and Wildlife Service, Division of Migratory Bird Management, 1011 East Tudor Road, MS 201, Anchorage, Alaska 99503 USA 3United States Fish and Wildlife Service, Division of Migratory Bird Management, 755 Parfet Street, Suite 235, Lakewood, Colorado 80215 USA 4United States Fish and Wildlife Service, Washington Maritime National Wildlife Refuge Complex, 715 Holgerson Road, Sequim, Washington 98382 USA Tessler, D.F., J.A. Johnson, B.A. Andres, S. Thomas, & R.B. Lanctot. 2014. A global assessment of the conser - vation status of the Black Oystercatcher Haematopus bachmani . International Wader Studies 20: 83 –96. The Black Oystercatcher Haematopus bachmani , a monotypic species, is one of the less studied members of the genus. The global population of roughly 10,000 individuals is scattered unevenly along the North American Pacific Ocean coast from the Aleutian Islands to Baja California, with the vast majority (about 80%) in Alaska and British Columbia. Favouring rocky shorelines in areas of high tidal variation, they forage exclusively on intertidal macroinvertebrates (e.g. limpets and mussels). Because they are completely dependent on marine shorelines, the Black Oystercatcher is considered a sensitive indicator of the health of the rocky intertidal community. Breeding oystercatchers are highly territorial, and nesting densities are generally low; however, during the winter months they tend to aggregate in groups of tens to hundreds. -
Alpha Codes for 2168 Bird Species (And 113 Non-Species Taxa) in Accordance with the 62Nd AOU Supplement (2021), Sorted Taxonomically
Four-letter (English Name) and Six-letter (Scientific Name) Alpha Codes for 2168 Bird Species (and 113 Non-Species Taxa) in accordance with the 62nd AOU Supplement (2021), sorted taxonomically Prepared by Peter Pyle and David F. DeSante The Institute for Bird Populations www.birdpop.org ENGLISH NAME 4-LETTER CODE SCIENTIFIC NAME 6-LETTER CODE Highland Tinamou HITI Nothocercus bonapartei NOTBON Great Tinamou GRTI Tinamus major TINMAJ Little Tinamou LITI Crypturellus soui CRYSOU Thicket Tinamou THTI Crypturellus cinnamomeus CRYCIN Slaty-breasted Tinamou SBTI Crypturellus boucardi CRYBOU Choco Tinamou CHTI Crypturellus kerriae CRYKER White-faced Whistling-Duck WFWD Dendrocygna viduata DENVID Black-bellied Whistling-Duck BBWD Dendrocygna autumnalis DENAUT West Indian Whistling-Duck WIWD Dendrocygna arborea DENARB Fulvous Whistling-Duck FUWD Dendrocygna bicolor DENBIC Emperor Goose EMGO Anser canagicus ANSCAN Snow Goose SNGO Anser caerulescens ANSCAE + Lesser Snow Goose White-morph LSGW Anser caerulescens caerulescens ANSCCA + Lesser Snow Goose Intermediate-morph LSGI Anser caerulescens caerulescens ANSCCA + Lesser Snow Goose Blue-morph LSGB Anser caerulescens caerulescens ANSCCA + Greater Snow Goose White-morph GSGW Anser caerulescens atlantica ANSCAT + Greater Snow Goose Intermediate-morph GSGI Anser caerulescens atlantica ANSCAT + Greater Snow Goose Blue-morph GSGB Anser caerulescens atlantica ANSCAT + Snow X Ross's Goose Hybrid SRGH Anser caerulescens x rossii ANSCAR + Snow/Ross's Goose SRGO Anser caerulescens/rossii ANSCRO Ross's Goose -
Coastal Wetlands Species Fact Sheet
TEXAS PARKS AND WILDLIFE Whooping Crane Grus americana TPWD PHOTO Whooping cranes are one of the rarest bird species in North America. Although they breed in Canada during the summer months, whooping cranes migrate to Texas’ coastal plains near Rockport for the winter months. COASTAL WETLANDS Whooping Crane Grus americana APPEARANCE BEHAVIOR Height: 5 feet (1.5 m) Whooping cranes begin their fall migration south to Texas in Wingspan: 7.5 feet (2.3 m) mid-September and begin the spring migration north to Canada in late March or early April. They mate for life, but will accept a Distinguishing Characteristics new mate if one dies. The mated pair shares brooding duties; • White with rust-colored patches on top and back of head either the male or the female is always on the nest. The hatch- • Black feathers on both sides of the head lings will stay with their parents throughout their first winter, • Yellow eyes and separate when the spring migration begins. The sub-adults • Primary wing feathers are black but are visible only in flight. form groups and travel together. • Long, black legs and bills NOW YOU KNOW! LIFE HISTORY • Whooping cranes live in “families” with two adult birds, a Range: Limited in Texas to the migratory flyway male and a female, and one or two of their young. Whooping and coastal plain around Aransas. cranes migrate more than 2,400 miles a year. Diet: Crabs, clams, crayfish, snails, minnows, • As many as 1,400 whooping cranes migrated across North frogs, larval insects and leeches; occa- America in the mid-1800s. -
The Role of Coastal Engineering in American Oystercatcher Conservation April 2016
THE ROLE OF COASTAL ENGINEERING IN AMERICAN OYSTERCATCHER CONSERVATION APRIL 2016 Chris Farrell Marianne Korosy Julie Wraithmell Audubon Florida Our mission is to conserve and restore natural ecosystems, focusing on birds, other wildlife, and their habitats for the benefit of humanity and the earth’s biological diversity. The production of this paper was supported by a grant from the National Fish and Wildlife Foundation. The views and conclusions contained in this document are those of the authors and should not be interpreted as representing the opinions or policies of the U.S. Government or the National Fish and Wildlife Foundation. Mention of trade names or commercial products does not constitute their endorsement by the U.S. Government or the National Fish and Wildlife Foundation. The Role of Coastal Engineering in American Oystercatcher Conservation Executive Summary Humans have engineered the coasts for centuries, trying to create stability for the built environment in a system that is inherently dynamic. Continued coastal development and sea level rise are increasing the demand for engineered coastlines. Simultaneously, restoration dollars made available by the Deepwater Horizon settlements in the Gulf of Mexico will likely fuel a boom of such projects—from oyster reefs to armoring. These projects are often designed to achieve one particular goal such as coastal protection, oyster restoration, or erosion control, yet often have unintended impacts that jeopardize declining populations of coastal wildlife. With advanced planning and consideration, coastal engineering projects can be designed to minimize impacts and in some cases provide benefits to these species. This report summarizes the impacts of coastal engineering on the American Oystercatcher and provides recommendations for permit applicants, project engineers, and regulatory reviewers to improve future projects for the benefit of these imperiled shorebirds.