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Wild Species 2010 the GENERAL STATUS of SPECIES in CANADA
Wild Species 2010 THE GENERAL STATUS OF SPECIES IN CANADA Canadian Endangered Species Conservation Council National General Status Working Group This report is a product from the collaboration of all provincial and territorial governments in Canada, and of the federal government. Canadian Endangered Species Conservation Council (CESCC). 2011. Wild Species 2010: The General Status of Species in Canada. National General Status Working Group: 302 pp. Available in French under title: Espèces sauvages 2010: La situation générale des espèces au Canada. ii Abstract Wild Species 2010 is the third report of the series after 2000 and 2005. The aim of the Wild Species series is to provide an overview on which species occur in Canada, in which provinces, territories or ocean regions they occur, and what is their status. Each species assessed in this report received a rank among the following categories: Extinct (0.2), Extirpated (0.1), At Risk (1), May Be At Risk (2), Sensitive (3), Secure (4), Undetermined (5), Not Assessed (6), Exotic (7) or Accidental (8). In the 2010 report, 11 950 species were assessed. Many taxonomic groups that were first assessed in the previous Wild Species reports were reassessed, such as vascular plants, freshwater mussels, odonates, butterflies, crayfishes, amphibians, reptiles, birds and mammals. Other taxonomic groups are assessed for the first time in the Wild Species 2010 report, namely lichens, mosses, spiders, predaceous diving beetles, ground beetles (including the reassessment of tiger beetles), lady beetles, bumblebees, black flies, horse flies, mosquitoes, and some selected macromoths. The overall results of this report show that the majority of Canada’s wild species are ranked Secure. -
Genetic Structure of Taiga Bean Goose in Central Scandinavia
Bird Conservation International, page 1 of 14. © BirdLife International, 2018 doi:10.1017/S0959270918000205 Birds of different feather flock together - genetic structure of Taiga Bean Goose in Central Scandinavia ADRIAAN DE JONG, ODDMUND KLEVEN, JAN EIVIND ØSTNES, ROLF TERJE KROGLUND, ISAK VAHLSTRÖM, JAN NILSSON and GÖRAN SPONG Summary During their flightless summer moult, Taiga Bean Geese Anser fabalis fabalis gather at commu- nal moulting sites. Individuals from the Nord-Trøndelag breeding area in Norway have been observed to join with local individuals on moulting sites in Vilhelmina Municipality, Sweden. These two groups show distinct features in breeding habitat and migratory behaviour, but are they also genetically distinct? We used 12 microsatellite loci for genotyping 109 blood, feather and faecal samples from three sampling areas (Røyrvik in Norway and Stalon and Nästansjö in Sweden) to examine genetic diversity and structure. Clustering and Principal Coordinate analyses of all samples unveiled at least two distinct clusters, which were unevenly distributed over the sampling sites. Grouped by sampling sites, AMOVA and FST analyses showed that samples from the three sites differed genetically. These differences were larger between Røyrvik and Nästansjö than between Stalon and the other two. Relatedness was high among the Røyrvik samples. From our results we conclude that one of the clusters describes the Røyrvik breeding subpopulation, while the other(s) breed mainly in Sweden. Although these subpopulations simultaneously use the same moulting area in Vilhelmina, they appear to be ecologically, behaviourally and genetically distinct, in particular the Røyrvik sub-population. For goose conservation and management, we suggest that the Nord-Trøndelag (Røyrvik) subpopulation is considered a separate flyway man- agement unit. -
Recent Introgression Between Taiga Bean Goose and Tundra Bean Goose Results in a Largely Homogeneous Landscape of Genetic Differentiation
Heredity (2020) 125:73–84 https://doi.org/10.1038/s41437-020-0322-z ARTICLE Recent introgression between Taiga Bean Goose and Tundra Bean Goose results in a largely homogeneous landscape of genetic differentiation 1 2 3 1 Jente Ottenburghs ● Johanna Honka ● Gerard J. D. M. Müskens ● Hans Ellegren Received: 12 December 2019 / Revised: 11 May 2020 / Accepted: 12 May 2020 / Published online: 26 May 2020 © The Author(s) 2020. This article is published with open access Abstract Several studies have uncovered a highly heterogeneous landscape of genetic differentiation across the genomes of closely related species. Specifically, genetic differentiation is often concentrated in particular genomic regions (“islands of differentiation”) that might contain barrier loci contributing to reproductive isolation, whereas the rest of the genome is homogenized by introgression. Alternatively, linked selection can produce differentiation islands in allopatry without introgression. We explored the influence of introgression on the landscape of genetic differentiation in two hybridizing goose taxa: the Taiga Bean Goose (Anser fabalis) and the Tundra Bean Goose (A. serrirostris). We re-sequenced the whole 1234567890();,: 1234567890();,: genomes of 18 individuals (9 of each taxon) and, using a combination of population genomic summary statistics and demographic modeling, we reconstructed the evolutionary history of these birds. Next, we quantified the impact of introgression on the build-up and maintenance of genetic differentiation. We found evidence for a scenario of allopatric divergence (about 2.5 million years ago) followed by recent secondary contact (about 60,000 years ago). Subsequent introgression events led to high levels of gene flow, mainly from the Tundra Bean Goose into the Taiga Bean Goose. -
4 East Dongting Lake P3-19
3 The functional use of East Dongting Lake, China, by wintering geese ANTHONY D. FOX1, CAO LEI2*, MARK BARTER3, EILEEN C. REES4, RICHARD D. HEARN4, CONG PEI HAO2, WANG XIN2, ZHANG YONG2, DOU SONG TAO2 & SHAO XU FANG2 1Department of Wildlife Ecology and Biodiversity, National Environmental Research Institute, University of Aarhus, Kalø, Grenåvej 14, DK-8410 Rønde, Denmark. 2School of Life Science, University of Science and Technology of China, Hefei, Anhui 230026, PR China. 321 Chivalry Avenue, Glen Waverley, Victoria 3150, Australia. 4Wildfowl and Wetlands Trust, Slimbridge, Gloucestershire GL2 7BT, UK. *Correspondence author. E-mail: [email protected] Abstract A survey and study of geese wintering at the East Dongting Lake National Nature Reserve, China, in February 2008 revealed internationally important numbers of Lesser White-fronted Geese Anser erythropus, Greater White-fronted Geese Anser albifrons and Bean Geese Anser fabilis using the site, as well as small numbers of Greylag Geese Anser anser. Only five Swan Geese Anser cygnoides were recorded, compared with several hundreds in the 1990s. Globally important numbers of Lesser White-fronted Geese spend the majority of daylight hours feeding on short grassland and sedge meadows within the core reserve areas of the National Nature Reserve, and also roost there at night. Greater White-fronted Geese were not studied in detail, but showed similar behaviour. Large numbers of Bean Geese of both serrirostris and middendorffi races showed differing feeding strategies. The small numbers of serrirostris tended to roost and feed in or near the reserve on short grassland, as did small proportions of middendorffi. However, the majority of middendorffi slept within the confines of the reserve by day and flew out at dusk, to nocturnal feeding areas at least 40 km north on the far side of the Yangtze River, returning 40–80 min after first light. -
The Mystery of Anser Neglectus Sushkin, 1897. Victim of the Tunguska Disaster? a Hungarian Story
Ornis Hungarica 2019. 27(2): 20–58. DOI: 10.2478/orhu-2019-0014 The mystery of Anser neglectus Sushkin, 1897. Victim of the Tunguska disaster? A Hungarian story Jacques VAN IMPE Received: April 08, 2019 – Revised: August 10, 2019 – Accepted: October 31, 2019 Van Impe, J. 2019. The mystery of Anser neglectus Sushkin, 1897. Victim of the Tunguska dis- aster? A Hungarian story. – Ornis Hungarica 27(2): 20–58. DOI: 10.2478/orhu-2019-0014 Abstract The well-known Russian ornithologist Prof. Peter Sushkin described it as a distinct species from Bashkortostan (Bashkiria) in 1897, a highly acclaimed discovery. However, its breeding grounds never been discovered. Since then, there has been a long-standing debate over the taxonom- ic position of Anser neglectus. Taxonomists have argued that Anser neglectus belongs to the group of A. fabalis Lath. because of its close resemblance with A. f. fabalis. At the beginning of the 20th century, large numbers of the Sushkin’s goose were observed in three winter quar- ters: on two lakes in the Republic of Bachkortostan, in the surroundings of the town of Tashkent in the Republic Uzbekistan, and in the puszta Hortobágy in eastern Hungary. It is a pity that taxonomists did not thoroughly com- pare the Russian and Hungarian ornithological papers concerning the former presence of Anser neglectus in these areas, because these rich sources refer to characteristics that would cast serious doubt on the classification ofAns - er neglectus as a subspecies, an individual variation or mutation of A. f. fabalis. Sushkin’s goose, though a typical Taiga Bean Goose, distinguished itself from other taxa of the Bean Goose by its plumage, its field identification, by its specific “Gé-gé” call, the size of its bill, and by its preference for warm and dry winter haunts. -
Notes on Indian Rarities–2: Waterfowl, Diving Waterbirds, and Gulls and Terns Praveen J., Rajah Jayapal & Aasheesh Pittie
Praveen et al. : Indian rarities–2 113 Notes on Indian rarities–2: Waterfowl, diving waterbirds, and gulls and terns Praveen J., Rajah Jayapal & Aasheesh Pittie Praveen J., Jayapal, R., & Pittie, A., 2014. Notes on Indian rarities—2: Waterfowl, diving waterbirds, and gulls and terns. Indian BIRDS 9 (5&6): 113–136. Praveen J., B303, Shriram Spurthi, ITPL Main Road, Brookefields, Bengaluru 560037, Karnataka, India. Email: [email protected]. [Corresponding author.] Rajah Jayapal, Sálim Ali Centre for Ornithology and Natural History, Anaikatty (Post), Coimbatore 641108, Tamil Nadu, India. Email: [email protected]. Aasheesh Pittie, 2nd Floor, BBR Forum, Road No. 2, Banjara Hills, Hyderabad 500034, Telangana, India. Email: [email protected]. [Continued from Indian BIRDS 8 (5): 125.] n this part, we present annotated notes on 36 species, from the published; this list will include all the species that have been Ifollowing families: reliably recorded, in an apparently wild state, in the country. In • Anatidae (Swans, geese, and ducks) addition, species from naturalised populations, either established • Podicipedidae (Grebes) within the country or outside, from which individual birds • Gaviidae (Loons) sometimes straggle to the region would also be included in the • Phalacrocoracidae (Cormorants) Checklist. For this part of the series, we have excluded some • Laridae (Gulls and terns) anatids that have become rare in recent years having undergone a grave population decline, but were widely reported in India during the nineteenth, and early twentieth centuries. This list Table 1. Abbreviations used in the text includes White-headed Duck Oxyura leucocephala, Baikal Teal Abbreviations Reference Anas formosa, Smew Mergellus albellus, Baer’s Pochard Aythya AWC Asian Waterbird Census (www.wetlands.org/awc) baeri, and Pink-headed Duck Rhodonessa caryophyllacea, BMNH Natural History Museum, London (www.nhm.ac.uk) the last now probably locally extinct. -
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107 Changes in numbers of staging and wintering geese in Sweden: 1977/78–2019/20 LEIF NILSSON1,* & HAKON KAMPE-PERSSON2 1Department of Biology, Biodiversity, University of Lund, Ecology Building, SE-223 62 Lund, Sweden. 2Pulma i, Gl das pagasts, Jelgavas novads, LV-3040 N kotne, Latvia. *Correspondence author. E-mail: [email protected] Abstract Regular goose counts made throughout Sweden since 1977/78 show that the total numbers staging and wintering in the country have increased markedly over the decades. October totals were of 51,000 geese in 1977, rising to c. 600,000 in 2018, during which time January totals also increased from 31,000 to 252,000 birds. The greatest change recorded was for the Greylag Goose Anser anser, numbers of which rose from 20,000 to > 250,000 individuals over a 35-year period. Changes in migration and wintering habits have also been recorded, with mid-winter (January) Greylag Goose numbers now amounting to 20–33% of the September totals in recent years, illustrating increases in the proportion of the population now wintering in the country. Moreover, large numbers of Barnacle Geese Branta leucopsis have started to stage and over-winter in Sweden, and are now becoming the commonest species, with 365,000 recorded in autumn 2019. Key words: autumn, goose counts, migration patterns, population increase, winter. During recent decades, most Northwest which was formerly widespread across European goose populations have increased the Scandinavian mountain chain but is markedly (Madsen et al. 1999; Fox et al. now reduced to very few breeding pairs, 2010; Fox & Madsen 2017; Fox & Leafloor mainly in Norway, with a re-introduced 2018), with some reaching levels where population occurring in Sweden (Andersson they have come into conflict with & Holmqvist 2010; Fox & Leafloor agriculture when feeding on crops causes 2018). -
Species Top 10S Ebird
Impatient Birder's Guide To North America - Species Top 10s eBird. 2012. eBird: An online database of bird distribution and abundance [web application]. eBird, Ithaca, New York. Available: http://www.ebird.org. (Accessed: February 22, 2013) Species Rank St/Prov Month Wk# % of Checklists Quality Black-bellied Whistling-Duck 1 TX Apr 4 14.55% Black-bellied Whistling-Duck 2 TX Jul 3 14.01% Black-bellied Whistling-Duck 3 TX Jul 2 13.98% Black-bellied Whistling-Duck 4 TX Apr 3 13.73% Black-bellied Whistling-Duck 5 TX Jul 4 13.50% Black-bellied Whistling-Duck 6 TX Jun 4 13.48% Black-bellied Whistling-Duck 7 TX Aug 1 13.21% Black-bellied Whistling-Duck 8 TX Apr 2 13.10% Black-bellied Whistling-Duck 9 TX Jun 1 13.10% Black-bellied Whistling-Duck 10 LA Jul 2 13.01% Fulvous Whistling-Duck 1 LA May 1 6.47% Fulvous Whistling-Duck 2 LA Apr 4 6.29% Fulvous Whistling-Duck 3 LA Jul 2 4.18% Fulvous Whistling-Duck 4 TX Apr 4 3.77% Fulvous Whistling-Duck 5 LA Jul 4 3.62% Fulvous Whistling-Duck 6 LA May 2 3.51% Fulvous Whistling-Duck 7 LA Jul 3 3.34% Fulvous Whistling-Duck 8 LA Jun 4 3.33% Fulvous Whistling-Duck 9 LA Apr 2 3.28% Fulvous Whistling-Duck 10 TX Apr 3 3.19% Taiga Bean-Goose 1 AK Oct 3 0.68% Taiga Bean-Goose 2 AK Dec 3 0.29% Taiga Bean-Goose 3 AK Feb 2 0.29% Taiga Bean-Goose 4 AK Mar 3 0.28% Taiga Bean-Goose 5 CA Nov 2 0.27% Taiga Bean-Goose 6 AK Oct 2 0.24% Taiga Bean-Goose 7 AK Nov 4 0.24% Taiga Bean-Goose 8 AK Sep 4 0.15% Taiga Bean-Goose 9 AK Mar 4 0.15% Taiga Bean-Goose 10 AK Apr 1 0.15% Tundra Bean-Goose 1 AK May 4 0.65% Tundra Bean-Goose 2 AK May 3 0.45% Tundra Bean-Goose 3 AK Jun 1 0.26% Compiled by Greg Miller. -
Response of Herbivorous Geese to Wintering Habitat Changes: Conservation Insights from Long-Term Population Monitoring in the East Dongting Lake, China
Reg Environ Change (2017) 17:879–888 DOI 10.1007/s10113-016-1087-z ORIGINAL ARTICLE Response of herbivorous geese to wintering habitat changes: conservation insights from long-term population monitoring in the East Dongting Lake, China 1,2,3 1,2 1,2 4 Ye-Ai Zou • Yue Tang • Yong-Hong Xie • Qi-Hong Zhao • Hong Zhang4 Received: 18 October 2015 / Accepted: 24 November 2016 / Published online: 2 December 2016 Ó Springer-Verlag Berlin Heidelberg 2016 Abstract The majority of Eastern China’s herbivorous fronted Geese were more sensitive to habitat changes. No geese overwinter in the East Dongting Lake, China, and significant correlations were observed between goose there is growing concern about how changes in their abundances and both mean water levels and sedge meadow habitats can affect the goose populations. General linear areas. Results indicate that the variations in herbivorous regressions were used to analyze the relationship between goose abundances may be caused by changes in the NDVI changes in the abundances of three herbivorous geese of sedge meadows and the interval durations between (Eastern Tundra Bean Goose Anser fabalis serrirostris, sedge meadow exposure and goose arrival. The earlier Lesser White-fronted Geese Anser erythropus, and Greater flood recession can accelerate the exposure, growth, and White-fronted Goose Anser albifrons frontalis) and their withering of sedge meadows (low NDVI in late January), wintering habitats in the East Dongting Lake during thereby creating unsuitable feeding conditions for the geese 2002/2003–2014/2015. The fluctuations in three herbivo- in the wintering seasons. These findings are important as rous goose abundances exhibited negative correlations with efforts are made to protect these valuable species from the changes in interval duration (i.e., days between complete effects of human intervention, and in particular, the Three sedge meadow exposure and goose arrival in the study Gorges Dam project. -
Systematic List of the Romanian Vertebrate Fauna
Travaux du Muséum National d’Histoire Naturelle © Décembre Vol. LIII pp. 377–411 «Grigore Antipa» 2010 DOI: 10.2478/v10191-010-0028-1 SYSTEMATIC LIST OF THE ROMANIAN VERTEBRATE FAUNA DUMITRU MURARIU Abstract. Compiling different bibliographical sources, a total of 732 taxa of specific and subspecific order remained. It is about the six large vertebrate classes of Romanian fauna. The first class (Cyclostomata) is represented by only four species, and Pisces (here considered super-class) – by 184 taxa. The rest of 544 taxa belong to Tetrapoda super-class which includes the other four vertebrate classes: Amphibia (20 taxa); Reptilia (31); Aves (382) and Mammalia (110 taxa). Résumé. Cette contribution à la systématique des vertébrés de Roumanie s’adresse à tous ceux qui sont intéressés par la zoologie en général et par la classification de ce groupe en spécial. Elle représente le début d’une thème de confrontation des opinions des spécialistes du domaine, ayant pour but final d’offrir aux élèves, aux étudiants, aux professeurs de biologie ainsi qu’à tous ceux intéressés, une synthèse actualisée de la classification des vertébrés de Roumanie. En compilant différentes sources bibliographiques, on a retenu un total de plus de 732 taxons d’ordre spécifique et sous-spécifique. Il s’agît des six grandes classes de vertébrés. La première classe (Cyclostomata) est représentée dans la faune de Roumanie par quatre espèces, tandis que Pisces (considérée ici au niveau de surclasse) l’est par 184 taxons. Le reste de 544 taxons font partie d’une autre surclasse (Tetrapoda) qui réunit les autres quatre classes de vertébrés: Amphibia (20 taxons); Reptilia (31); Aves (382) et Mammalia (110 taxons). -
HELCOM Red List
SPECIES INFORMATION SHEET Anser fabalis fabalis (wintering) English name: Scientific name: Taiga Bean Goose Anser fabalis fabalis (wintering population) Taxonomical group: Species authority: Class: Aves Latham, 1787 Order: Anseriformes Family: Anatidae Subspecies, Variations, Synonyms: – Generation length: 6 years Past and current threats (Habitats Directive Future threats (Habitats Directive article 17 article 17 codes): codes): Hunting (F03.01), Human disturbance (G01), Hunting (F03.01), Human disturbance (G01), Overgrowth of open areas (A04.03), Mining and Overgrowth of open areas (A04.03), Mining and quarrying (C01.03), Construction (J02.12, C02), quarrying (C01.03), Construction (J02.12, C02), Other threat factors (Loss of specific habitat Other threat factors (Loss of specific habitat features, J03.01), Contaminant pollution (A07), features, J03.01), Contaminant pollution (A07), Extra-regional threats (XO) Extra-regional threats (XO) IUCN Criteria: HELCOM Red List EN A2b Category: Endangered Global / European IUCN Red List Category EU Birds Directive: LC / LC Annex II A Protection and Red List status in HELCOM countries: According to the Birds Directive (Annex II A) may be hunted in the EU Member States. Denmark: – (on the 1997 Danish Amber List as a species of national responsibility outside the breeding season), Estonia: VU, Finland: NT, Germany:“particularly protected” under Federal Species Protection Decree (Bundesartenschutzverordnung)/–, Latvia: –, Lithuania: –, Poland: –, Russia: –, Sweden: NT (breeding/resting) Range description and general trends The taiga bean goose Anser fabalis fabalis breeds in apparently two separate breeding populations in the Taiga zone of northern Scandinavia and of NW Siberia. Scandinavian birds mainly winter in S Sweden, with smaller numbers migrating to Denmark, Germany, The Netherlands and Great Britain. -
Proposals 2018-C
AOS Classification Committee – North and Middle America Proposal Set 2018-C 1 March 2018 No. Page Title 01 02 Adopt (a) a revised linear sequence and (b) a subfamily classification for the Accipitridae 02 10 Split Yellow Warbler (Setophaga petechia) into two species 03 25 Revise the classification and linear sequence of the Tyrannoidea (with amendment) 04 39 Split Cory's Shearwater (Calonectris diomedea) into two species 05 42 Split Puffinus boydi from Audubon’s Shearwater P. lherminieri 06 48 (a) Split extralimital Gracula indica from Hill Myna G. religiosa and (b) move G. religiosa from the main list to Appendix 1 07 51 Split Melozone occipitalis from White-eared Ground-Sparrow M. leucotis 08 61 Split White-collared Seedeater (Sporophila torqueola) into two species (with amendment) 09 72 Lump Taiga Bean-Goose Anser fabalis and Tundra Bean-Goose A. serrirostris 10 78 Recognize Mexican Duck Anas diazi as a species 11 87 Transfer Loxigilla portoricensis and L. violacea to Melopyrrha 12 90 Split Gray Nightjar Caprimulgus indicus into three species, recognizing (a) C. jotaka and (b) C. phalaena 13 93 Split Barn Owl (Tyto alba) into three species 14 99 Split LeConte’s Thrasher (Toxostoma lecontei) into two species 15 105 Revise generic assignments of New World “grassland” sparrows 1 2018-C-1 N&MA Classification Committee pp. 87-105 Adopt (a) a revised linear sequence and (b) a subfamily classification for the Accipitridae Background: Our current linear sequence of the Accipitridae, which places all the kites at the beginning, followed by the harpy and sea eagles, accipiters and harriers, buteonines, and finally the booted eagles, follows the revised Peters classification of the group (Stresemann and Amadon 1979).