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1 multiple forms of uric acid in hyperuricemic geese.
2 equency (exponent 7) of migratory bar-headed geese.
3 the stopover schedule of individual Barnacle Geese.
4 affect growth rates and offspring fitness in geese.
5 ed survival and fecundity for arctic-nesting geese.
6 s in black brent (Branta bernicla nigricans) geese.
7 rds most frequently detected in mallards and geese.
8  Two H5N1 viruses were isolated from healthy geese.
9 mmunity resistance to disturbance by grazing geese.
10 losely to the small-bodied lineage of Canada geese.
11 ulted in the deaths of up to 50% of infected geese.
12 tained by swabbing the cages that housed the geese.
13 lla anatipestifera-like disease in ducks and geese.
14  distribution changes of wintering waterfowl geese, 2) increase the outbreak risk in remaining sites
15 peruricemic blood in vitro and hyperuricemic geese, a native uricase via extracorporeal delivery was
16                              Arctic-breeding geese acquire resources for egg production from overwint
17 s including mastodons, reindeer, rodents and geese, all ancestral to their present-day and late Pleis
18 , revealing unique behavioral responses from geese among different habitats.
19 ance and spatial distribution of lesser snow geese (an alternative prey source), and spring climate o
20 ted IgM in serum samples from two species of geese and from experimentally infected ring-necked pheas
21 ual defenses against herbivory by flightless geese and goose-like ducks that were extirpated by Polyn
22 wastewater effluent and, to a lesser extent, geese and gull wastes.
23  of starlings and the simple-V formations of geese and other large migratory birds.
24 nd cloacal swabs of healthy chickens, ducks, geese and pigeons were collected nationwide from live-an
25 c reconstructions of variant MC1R alleles in geese and skuas show that melanism is a derived trait th
26 l protein sequences for 112 Anatidae (ducks, geese and swans) species, a biologically complex group o
27 and the potential role of domestic ducks and geese and wild waterfowl in the epidemiology of aMPV, we
28 and case studies (influenza A in lesser snow geese and Yersinia pestis in coyotes), we argue that wit
29 by reduced forage quality than larger-bodied geese, and (ii) goslings from subarctic brood-rearing ar
30 rkets (mostly chicken, pigeon, quail, ducks, geese, and a wide range of exotic wild-caught and farm-r
31 ulation modelling of Greenland white-fronted geese (Anser albifrons flavirostris) at their largest wi
32 were collected from 56 greater white-fronted geese (Anser albifrons frontalis) across seven ecologica
33  plumage polymorphisms in birds, lesser snow geese (Anser c. caerulescens) and arctic skuas (Stercora
34                                          The geese appear to have ample cardiac reserves, as heart ra
35                            Nesting migratory geese are among the dominant herbivores in (sub) arctic
36  test the hypotheses that (i) smaller-bodied geese are more negatively affected by reduced forage qua
37                Our assessment indicates that geese are recovering from habitat degradation by moving
38 ring when predictability was higher and when geese attempted breeding that year.
39 mercury (Hg) in eggs of herbivorous barnacle geese ( Branta leucopsis) from an island colony on Svalb
40 acal swab and brain samples from wild Canada geese (Branta canadensis) for ABV.
41 eport the resting metabolic rate in barnacle geese (Branta leucopsis) and provide evidence for the si
42 ich a rapidly growing population of barnacle geese (Branta leucopsis) responded to strong environment
43                                     Barnacle geese (Branta leucopsis) were tracked with solar GPS/ARG
44 ) to demographic data from Svalbard barnacle geese (Branta leucopsis), to quantify their population-d
45  and a selective vertebrate grazer (barnacle geese, Branta leucopsis).
46                                              Geese breeding in the Arctic have to do so in a short ti
47   Transmission of Go/Gd-like H5N1 viruses to geese by contact with infected geese resulted in infecti
48 materia and Polysticta species), and emperor geese (Chen canagica)), ages (adults higher than juvenil
49 emarkable behavior, we imprinted and trained geese, collecting the first cardiorespiratory measuremen
50 eocoastal peoples used such tools to capture geese, cormorants, and other birds, along with marine ma
51               The Hawaiian lineage of Canada geese diverged more dramatically, splitting into at leas
52 roduction of digestible biomass for barnacle geese during the staging period increased in Vesteralen
53 cardiorespiratory measurements of bar-headed geese flying at simulated altitude in a wind tunnel.
54 n witnessed specific migratory events (e.g., geese flying in their characteristic V-formations).
55 en following a large-scale exodus of nesting geese from the eider colony.
56 us (aMPV) recently isolated from wild Canada geese (goose 15a/01) in the United States, together with
57        Three other aMPV isolates from Canada geese had similarly large G genes, whereas analysis of r
58           In some areas the overabundance of geese has led to a drastic reduction in available forage
59 se actions, the increasing abundance of snow geese has since induced a state of satiation in harvest
60  and destructive foraging behaviours of snow geese have created a trophic cascade that reduces (sub-)
61 of the devastating trophic cascade that snow geese have triggered.
62 wever, some species, such as Arctic-breeding geese, have thrived during this period.
63 hat perished in a die-off of Canada and Snow geese in Cambridge Bay, Nunavut, Canada.
64 of A/goose/Guangdong/1/1996 (H5N1) in farmed geese in southern China, highly pathogenic H5N1 avian in
65 dnaviruses were cloned from exotic ducks and geese, including the Chiloe wigeon, mandarin duck, puna
66               Records of individually marked geese indicate that from the initial years of colonizati
67           Our findings suggest that barnacle geese integrate socially learned behaviour with adjustme
68                                   Bar-headed geese lower their flight metabolic rates to fly in low-o
69 sed by apparent competition with lesser snow geese, mediated by shared predators.
70 ngi fruiting, insects biting, fish spawning, geese migrating, deer calving; our consciousness is stee
71 d a previously unknown radiation of Hawaiian geese, of which only one representative remains alive (t
72 ng of migratory movements of Arctic breeding geese on different flyways to examine whether flyways di
73 tes or swabs were collected from wild ducks, geese, owls, sparrows, swallows, and starlings and from
74 l migration like that of its living duck and geese relatives, or it may have been a year-round reside
75 N1 viruses to geese by contact with infected geese resulted in infection of all birds but limited sig
76  whereas the two Nearctic lineages of Canada geese share a primitive plumage pattern.
77 PV RNA was detected in samples examined from geese, sparrows, and starlings.
78 Since the mid-1990s, an increasing number of geese stage in another area 250 km further north, Vester
79                  Historically, juvenile snow geese suffered from density-related degradation of their
80 episodes of 14 populations of ten species of geese, swans and dabbling ducks throughout Europe, East
81                                     However, geese tend to adopt a partial capital breeding strategy
82 rs of colonization onwards, especially young geese tended to switch to Vesteralen, thereby predominat
83 rabundant breeding population of lesser snow geese that has dramatically damaged the ecosystem, with
84  March 1999, this monitoring system detected geese that were serologically positive for H5N1 avian in
85 ith the aim of controlling overabundant snow geese, the Conservation Order amendment to the Internati
86 tory escape", i.e., the migration allows the geese to "escape" from the location where infection risk
87                   Transmission from infected geese to chickens occurred only by fecal contact, wherea
88 c conditions at subsequent stopovers enables geese to closely track the green wave.
89  and demographic rates of Greenland barnacle geese to discern the role of climate shifts in the popul
90 Results indicate avian sources (i.e., gulls, geese) to be the largest nonpoint source of FIB associat
91        The green wave hypothesis posits that geese track a successively delayed spring flush of plant
92                                 We find that geese track neither the onset of spring nor the peak in
93 s on cause-specific mortality in lesser snow geese using multistate capture-reencounter methods.
94 ks, Mallard ducks, Muscovy ducks, and Embden geese with 10(6) 50% egg infective doses of the A/Anhui/