USFWS DRAFT ENVIRONMENTAL ASSESSMENT Issuance of An
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TREND NOTE Number 021, October 2012
SCOTTISH NATURAL HERITAGE TREND NOTE Number 021, October 2012 SEABIRDS IN SCOTLAND Prepared by Simon Foster and Sue Marrs of SNH Knowledge Information Management Unit using results from the Seabird Monitoring Programme and the Joint Nature Conservation Committee Scotland has internationally important populations of several seabirds. Their conservation is assisted through a network of designated sites. Figure 1 shows the distribution of the 50 Special Protection Areas (SPA) which have seabirds listed as a feature of interest. The map shows the widespread nature of the sites and the predominance of important seabird areas on the Northern Isles (Orkney and Shetland), where some of our largest seabird colonies are present. The most recent estimate of seabird populations was obtained from Birds of Scotland (Forrester et al., 2007). Table 1 shows the population levels for all seabirds regularly breeding in Scotland. Table 1: Population Estimates for Breeding Seabirds in Scotland. Figure 1: Special Protection Areas for Seabirds Breeding in Scotland. Species* Unit** Estimate Key Points Northern fulmar 486,000 AOS Manx shearwater 126,545 AOS Trends are described for 11 of the 24 European storm-petrel 31,570+ AOS species of seabirds breeding in Leach’s storm-petrel 48,057 AOS Scotland Northern gannet 182,511 AOS Great cormorant c. 3,600 AON Nine have shown sustained declines European shag 21,500-30,000 PAIRS over the past 20 years. Two have Arctic skua 2,100 AOT remained stable. Great skua 9,650 AOT The reasons for the declines are Black headed -
Conservation Problems on Tristan Da Cunha Byj
28 Oryx Conservation Problems on Tristan da Cunha ByJ. H. Flint The author spent two years, 1963-65, as schoolmaster on Tristan da Cunha, during which he spent four weeks on Nightingale Island. On the main island he found that bird stocks were being depleted and the islanders taking too many eggs and young; on Nightingale, however, where there are over two million pairs of great shearwaters, the harvest of these birds could be greater. Inaccessible Island, which like Nightingale, is without cats, dogs or rats, should be declared a wildlife sanctuary. Tl^HEN the first permanent settlers came to Tristan da Cunha in " the early years of the nineteenth century they found an island rich in bird and sea mammal life. "The mountains are covered with Albatross Mellahs Petrels Seahens, etc.," wrote Jonathan Lambert in 1811, and Midshipman Greene, who stayed on the island in 1816, recorded in his diary "Sea Elephants herding together in immense numbers." Today the picture is greatly changed. A century and a half of human habitation has drastically reduced the larger, edible species, and the accidental introduction of rats from a shipwreck in 1882 accelerated the birds' decline on the main island. Wood-cutting, grazing by domestic stock and, more recently, fumes from the volcano have destroyed much of the natural vegetation near the settlement, and two bird subspecies, a bunting and a flightless moorhen, have become extinct on the main island. Curiously, one is liable to see more birds on the day of arrival than in several weeks ashore. When I first saw Tristan from the decks of M.V. -
Puffinus Gravis (Great Shearwater)
Maine 2015 Wildlife Action Plan Revision Report Date: January 13, 2016 Puffinus gravis (Great Shearwater) Priority 3 Species of Greatest Conservation Need (SGCN) Class: Aves (Birds) Order: Procellariiformes (Tubenoses) Family: Procellariidae (Fulmers, Petrels, And Shearwaters) General comments: Status seems secure though limited data Species Conservation Range Maps for Great Shearwater: Town Map: Puffinus gravis_Towns.pdf Subwatershed Map: Puffinus gravis_HUC12.pdf SGCN Priority Ranking - Designation Criteria: Risk of Extirpation: NA State Special Concern or NMFS Species of Concern: NA Recent Significant Declines: NA Regional Endemic: NA High Regional Conservation Priority: North American Waterbird Conservation Plan: High Concern United States Birds of Conservation Concern: Bird of Conservation Concern in Bird Conservation Regions 14 and/or 30: Yes High Climate Change Vulnerability: NA Understudied rare taxa: NA Historical: NA Culturally Significant: NA Habitats Assigned to Great Shearwater: Formation Name Cliff & Rock Macrogroup Name Rocky Coast Formation Name Subtidal Macrogroup Name Subtidal Pelagic (Water Column) Habitat System Name: Offshore **Primary Habitat** Stressors Assigned to Great Shearwater: No Stressors Currently Assigned to Great Shearwater or other Priority 3 SGCN. Species Level Conservation Actions Assigned to Great Shearwater: No Species Specific Conservation Actions Currently Assigned to Great Shearwater or other Priority 3 SGCN. Guild Level Conservation Actions: This Species is currently not attributed to a guild. -
Red-Footed Booby Helper at Great Frigatebird Nests
264 SHORT COMMUNICATIONS NECTS MEANS ECTS MEANS ICATE SAMPLE SIZE S.D. SAMPLE SIZE 70 IN DAYS FIGURE 2. Culmen length against age of Brown FIGURE 1. Weight against age of Brown Noddy Noddy chicks on Manana Island, Hawaii in 1972. chicks on Manana Island, Hawaii in 1972. about the thirty-fifth day; apparently Brown Noddies on Christmas Island grow more rapidly than those on 5.26 g/day (SD = 1.18 g/day), and chick growth rate Manana. More data are required for a refined analysis and fledging age were negatively correlated (r = of intraspecific variation in growth rates of Brown -0.490, N = 19, P < 0.05). Noddy young. Seventeen of the chicks were weighed both at the This paper is based upon my doctoral dissertation age of fledging and from 3 to 12 days later; there was submitted to the University of Hawaii. I thank An- no significant recession in weight after fledging (t = drew J. Berger for guidance and criticism. The 1.17, P > 0.2), as suggested for certain terns (e.g., Hawaii State Division of Fish and Game kindly LeCroy and LeCroy 1974, Bird-Banding 45:326). granted me permission to work on Manana. This Dorward and Ashmole (1963, Ibis 103b: 447) mea- study was supported by the Department of Zoology sured growth in weight and culmen length of Brown of the University of Hawaii, by an NSF Graduate Noddies on Ascension Island in the Atlantic; scatter Fellowship, and by a Mount Holyoke College Faculty diagrams of their data indicate growth functions very Grant. -
Copulation and Mate Guarding in the Northern Fulmar
COPULATION AND MATE GUARDING IN THE NORTHERN FULMAR SCOTT A. HATCH Museumof VertebrateZoology, University of California,Berkeley, California 94720 USA and AlaskaFish and WildlifeResearch Center, U.S. Fish and WildlifeService, 1011 East Tudor Road, Anchorage,Alaska 99503 USA• ABSTRACT.--Istudied the timing and frequency of copulation in mated pairs and the occurrenceof extra-paircopulation (EPC) among Northern Fulmars (Fulmarus glacialis) for 2 yr. Copulationpeaked 24 days before laying, a few daysbefore females departed on a prelaying exodus of about 3 weeks. I estimated that females were inseminated at least 34 times each season.A total of 44 EPC attemptswas seen,9 (20%)of which apparentlyresulted in insem- ination.Five successful EPCs were solicitated by femalesvisiting neighboring males. Multiple copulationsduring a singlemounting were rare within pairsbut occurredin nearly half of the successfulEPCs. Both sexesvisited neighborsduring the prelayingperiod, and males employed a specialbehavioral display to gain acceptanceby unattended females.Males investedtime in nest-siteattendance during the prelaying period to guard their matesand pursueEPC. However, the occurrenceof EPC in fulmars waslargely a matter of female choice. Received29 September1986, accepted 16 February1987. THEoccurrence and significanceof extra-pair Bjorkland and Westman 1983; Buitron 1983; copulation (EPC) in monogamousbirds has Birkhead et al. 1985). generated much interest and discussion(Glad- I attemptedto documentthe occurrenceand stone 1979; Oring 1982; Ford 1983; McKinney behavioral contextof extra-pair copulationand et al. 1983, 1984). Becausethe males of monog- mate guarding in a colonial seabird,the North- amous species typically make a large invest- ern Fulmar (Fulmarus glacialis). Fulmars are ment in the careof eggsand young, the costof among the longest-lived birds known, and fi- being cuckolded is high, as are the benefits to delity to the same mate and nest site between the successfulcuckolder. -
Sooty Shearwater Puffinus Griseus Few Changes in Bird Distribution
110 Petrels and Shearwaters — Family Procellariidae Sooty Shearwater Puffinus griseus birds are picked up regularly on the county’s beaches. Few changes in bird distribution have been as sud- Winter: From December to March the Sooty Shearwater den and dramatic as the Sooty Shearwater’s deser- is rare—currently much scarcer than the Short-tailed tion of the ocean off southern California. Before the Shearwater. Before 1982, winter counts ranged up to 20 1980s, this visitor from the southern hemisphere off San Diego 18 January 1969 (AFN 23:519, 1969). Since was the most abundant seabird on the ocean off San 1987, the highest winter count has been of three between San Diego and Los Coronados Islands 6 January 1995 (G. Diego in summer. After El Niño hit in 1982–83 and McCaskie). the ocean remained at an elevated temperature for the next 20 years, the shearwater’s numbers dropped Conservation: The decline of the Sooty Shearwater by 90% (Veit et al. 1996). A comparison confined followed quickly on the heels of the decline in ocean to the ocean near San Diego County’s coast would productivity off southern California that began in the likely show a decline even steeper. late 1970s: a decrease in zooplankton of 80% from 1951 to 1993 (Roemich and McGowan 1995, McGowan et al. Migration: The Sooty Shearwater begins arriving in April, 1998). The shearwater’s declines were especially steep in peaks in May (Briggs et al. 1987), remains (or remained) years of El Niño, and from 1990 on there was no recov- common through September, and then decreases in ery even when the oceanographic pendulum swung the number through December. -
Seabirds in Southeastern Hawaiian Waters
WESTERN BIRDS Volume 30, Number 1, 1999 SEABIRDS IN SOUTHEASTERN HAWAIIAN WATERS LARRY B. SPEAR and DAVID G. AINLEY, H. T. Harvey & Associates,P.O. Box 1180, Alviso, California 95002 PETER PYLE, Point Reyes Bird Observatory,4990 Shoreline Highway, Stinson Beach, California 94970 Waters within 200 nautical miles (370 km) of North America and the Hawaiian Archipelago(the exclusiveeconomic zone) are consideredas withinNorth Americanboundaries by birdrecords committees (e.g., Erickson and Terrill 1996). Seabirdswithin 370 km of the southern Hawaiian Islands (hereafterreferred to as Hawaiian waters)were studiedintensively by the PacificOcean BiologicalSurvey Program (POBSP) during 15 monthsin 1964 and 1965 (King 1970). Theseresearchers replicated a tracklineeach month and providedconsiderable information on the seasonaloccurrence and distributionof seabirds in these waters. The data were primarily qualitative,however, because the POBSP surveyswere not basedon a strip of defined width nor were raw counts corrected for bird movement relative to that of the ship(see Analyses). As a result,estimation of density(birds per unit area) was not possible. From 1984 to 1991, using a more rigoroussurvey protocol, we re- surveyedseabirds in the southeasternpart of the region (Figure1). In this paper we providenew informationon the occurrence,distribution, effect of oceanographicfactors, and behaviorof seabirdsin southeasternHawai- ian waters, includingdensity estimatesof abundant species. We also document the occurrenceof six speciesunrecorded or unconfirmed in thesewaters, the ParasiticJaeger (Stercorarius parasiticus), South Polar Skua (Catharacta maccormicki), Tahiti Petrel (Pterodroma rostrata), Herald Petrel (P. heraldica), Stejneger's Petrel (P. Iongirostris), and Pycroft'sPetrel (P. pycrofti). STUDY AREA AND SURVEY PROTOCOL Our studywas a piggybackproject conducted aboard vessels studying the physicaloceanography of the easterntropical Pacific. -
The Taxonomy of the Procellariiformes Has Been Proposed from Various Approaches
山 階 鳥 研 報(J. Yamashina Inst. Ornithol.),22:114-23,1990 Genetic Divergence and Relationships in Fifteen Species of Procellariiformes Nagahisa Kuroda*, Ryozo Kakizawa* and Masayoshi Watada** Abstract The genetic analysis of 23 protein loci in 15 species of Procellariiformes was made The genetic distancesbetween the specieswas calculatedand a dendrogram was formulated of the group. The separation of Hydrobatidae from all other taxa including Diomedeidae agrees with other precedent works. The resultsof the present study support the basic Procellariidclassification system. However, two points stillneed further study. The firstpoint is that Fulmarus diverged earlier from the Procellariidsthan did the Diomedeidae. The second point is the position of Puffinuspacificus which appears more closely related to the Pterodroma petrels than to other Puffinus species. These points are discussed. Introduction The taxonomy of the Procellariiformes has been proposed from various approaches. The earliest study by Forbes (1882) was made by appendicular myology. Godman (1906) and Loomis (1918) studied this group from a morphological point of view. The taxonomy of the Procellariiformes by functional osteology and appendicular myology was studied by Kuroda (1954, 1983) and Klemm (1969), The results of the various studies agreed in proposing four families of Procellariiformes: Diomedeidae, Procellariidae, Hydrobatidae, and Pelecanoididae. They also pointed out that the Procellariidae was a heterogenous group among them. Timmermann (1958) found the parallel evolution of mallophaga and their hosts in Procellariiformes. Recently, electrophoretical studies have been made on the Procellariiformes. Harper (1978) found different patterns of the electromorph among the families. Bar- rowclough et al. (1981) studied genetic differentiation among 12 species of Procellari- iformes at 16 loci, and discussed the genetic distances among the taxa but with no consideration of their phylogenetic relationships. -
Tube-Nosed Seabirds) Unique Characteristics
PELAGIC SEABIRDS OF THE CALIFORNIA CURRENT SYSTEM & CORDELL BANK NATIONAL MARINE SANCTUARY Written by Carol A. Keiper August, 2008 Cordell Bank National Marine Sanctuary protects an area of 529 square miles in one of the most productive offshore regions in North America. The sanctuary is located approximately 43 nautical miles northwest of the Golden Gate Bridge, and San Francisco California. The prominent feature of the Sanctuary is a submerged granite bank 4.5 miles wide and 9.5 miles long, which lay submerged 115 feet below the ocean’s surface. This unique undersea topography, in combination with the nutrient-rich ocean conditions created by the physical process of upwelling, produces a lush feeding ground. for countless invertebrates, fishes (over 180 species), marine mammals (over 25 species), and seabirds (over 60 species). The undersea oasis of the Cordell Bank and surrounding waters teems with life and provides food for hundreds of thousands of seabirds that travel from the Farallon Islands and the Point Reyes peninsula or have migrated thousands of miles from Alaska, Hawaii, Australia, New Zealand, and South America. Cordell Bank is also known as the albatross capital of the Northern Hemisphere because numerous species visit these waters. The US National Marine Sanctuaries are administered and managed by the National Oceanic and Atmospheric Administration (NOAA) who work with the public and other partners to balance human use and enjoyment with long-term conservation. There are four major orders of seabirds: 1) Sphenisciformes – penguins 2) *Procellariformes – albatross, fulmars, shearwaters, petrels 3) Pelecaniformes – pelicans, boobies, cormorants, frigate birds 4) *Charadriiformes - Gulls, Terns, & Alcids *Orders presented in this seminar In general, seabirds have life histories characterized by low productivity, delayed maturity, and relatively high adult survival. -
Tinamiformes – Falconiformes
LIST OF THE 2,008 BIRD SPECIES (WITH SCIENTIFIC AND ENGLISH NAMES) KNOWN FROM THE A.O.U. CHECK-LIST AREA. Notes: "(A)" = accidental/casualin A.O.U. area; "(H)" -- recordedin A.O.U. area only from Hawaii; "(I)" = introducedinto A.O.U. area; "(N)" = has not bred in A.O.U. area but occursregularly as nonbreedingvisitor; "?" precedingname = extinct. TINAMIFORMES TINAMIDAE Tinamus major Great Tinamou. Nothocercusbonapartei Highland Tinamou. Crypturellus soui Little Tinamou. Crypturelluscinnamomeus Thicket Tinamou. Crypturellusboucardi Slaty-breastedTinamou. Crypturellus kerriae Choco Tinamou. GAVIIFORMES GAVIIDAE Gavia stellata Red-throated Loon. Gavia arctica Arctic Loon. Gavia pacifica Pacific Loon. Gavia immer Common Loon. Gavia adamsii Yellow-billed Loon. PODICIPEDIFORMES PODICIPEDIDAE Tachybaptusdominicus Least Grebe. Podilymbuspodiceps Pied-billed Grebe. ?Podilymbusgigas Atitlan Grebe. Podicepsauritus Horned Grebe. Podicepsgrisegena Red-neckedGrebe. Podicepsnigricollis Eared Grebe. Aechmophorusoccidentalis Western Grebe. Aechmophorusclarkii Clark's Grebe. PROCELLARIIFORMES DIOMEDEIDAE Thalassarchechlororhynchos Yellow-nosed Albatross. (A) Thalassarchecauta Shy Albatross.(A) Thalassarchemelanophris Black-browed Albatross. (A) Phoebetriapalpebrata Light-mantled Albatross. (A) Diomedea exulans WanderingAlbatross. (A) Phoebastriaimmutabilis Laysan Albatross. Phoebastrianigripes Black-lootedAlbatross. Phoebastriaalbatrus Short-tailedAlbatross. (N) PROCELLARIIDAE Fulmarus glacialis Northern Fulmar. Pterodroma neglecta KermadecPetrel. (A) Pterodroma -
Important Bird Areas in Hawaii Elepaio Article
Globally Important Bird Areas in the Hawaiian Islands: Final Report Dr. Eric A. VanderWerf Pacific Rim Conservation 3038 Oahu Avenue Honolulu, HI 96822 9 June 2008 Prepared for the National Audubon Society, Important Bird Areas Program, Audubon Science, 545 Almshouse Road, Ivyland, PA 18974 3 of the 17 globally Important Bird Areas in Hawai`i, from top to bottom: Lehua Islet Hanawī Natural Area Reserve, Maui Hanalei National Wildlife Refuge, Kauai All photos © Eric VanderWerf Hawaii IBAs VanderWerf - 2 INTRODUCTION TO THE IMPORTANT BIRD AREAS PROGRAM The Important Bird Areas (IBA) Program is a global effort developed by BirdLife International, a global coalition of partner organizations in more than 100 countries, to assist with identification and conservation of areas that are vital to birds and other biodiversity. The IBA Program was initiated by BirdLife International in Europe in the 1980's. Since then, over 8,000 sites in 178 countries have been identified as Important Bird Areas, with many national and regional IBA inventories published in 19 languages. Hundreds of these sites and millions of acres have received better protection as a result of the IBA Program. As the United States Partner of BirdLife International, the National Audubon Society administers the IBA Program in the U.S., which was launched in 1995 (see http://www.audubon.org/bird/iba/index.html). Forty-eight states have initiated IBA programs, and more than 2,100 state-level IBAs encompassing over 220 million acres have been identified across the country. Information about these sites will be reviewed by the U.S. IBA Committee to confirm whether they qualify for classification as sites of continental or global significance. -
Iucn Red Data List Information on Species Listed On, and Covered by Cms Appendices
UNEP/CMS/ScC-SC4/Doc.8/Rev.1/Annex 1 ANNEX 1 IUCN RED DATA LIST INFORMATION ON SPECIES LISTED ON, AND COVERED BY CMS APPENDICES Content General Information ................................................................................................................................................................................................................................ 2 Species in Appendix I ............................................................................................................................................................................................................................... 3 Mammalia ............................................................................................................................................................................................................................................ 4 Aves ...................................................................................................................................................................................................................................................... 7 Reptilia ............................................................................................................................................................................................................................................... 12 Pisces .................................................................................................................................................................................................................................................