ライフサイエンスコーパス: geese

1 the stopover schedule of individual Barnacle Geese.

2 affect growth rates and offspring fitness in geese.

3 ed survival and fecundity for arctic-nesting geese.

4 s in black brent (Branta bernicla nigricans) geese.

5 Two H5N1 viruses were isolated from healthy geese.

6 mmunity resistance to disturbance by grazing geese.

7 losely to the small-bodied lineage of Canada geese.

8 ulted in the deaths of up to 50% of infected geese.

9 multiple forms of uric acid in hyperuricemic geese.

10 tained by swabbing the cages that housed the geese.

11 equency (exponent 7) of migratory bar-headed geese.

12 peruricemic blood in vitro and hyperuricemic geese, a native uricase via extracorporeal delivery was

13 ance and spatial distribution of lesser snow geese (an alternative prey source), and spring climate o

14 ted IgM in serum samples from two species of geese and from experimentally infected ring-necked pheas

15 ual defenses against herbivory by flightless geese and goose-like ducks that were extirpated by Polyn

16 wastewater effluent and, to a lesser extent, geese and gull wastes.

17 nd cloacal swabs of healthy chickens, ducks, geese and pigeons were collected nationwide from live-an

18 c reconstructions of variant MC1R alleles in geese and skuas show that melanism is a derived trait th

19 and the potential role of domestic ducks and geese and wild waterfowl in the epidemiology of aMPV, we

20 and case studies (influenza A in lesser snow geese and Yersinia pestis in coyotes), we argue that wit

21 by reduced forage quality than larger-bodied geese, and (ii) goslings from subarctic brood-rearing ar

22 rkets (mostly chicken, pigeon, quail, ducks, geese, and a wide range of exotic wild-caught and farm-r

23 ulation modelling of Greenland white-fronted geese (Anser albifrons flavirostris) at their largest wi

24 plumage polymorphisms in birds, lesser snow geese (Anser c. caerulescens) and arctic skuas (Stercora

25 Nesting migratory geese are among the dominant herbivores in (sub) arctic

26 test the hypotheses that (i) smaller-bodied geese are more negatively affected by reduced forage qua

27 Our assessment indicates that geese are recovering from habitat degradation by moving

28 ring when predictability was higher and when geese attempted breeding that year.

29 acal swab and brain samples from wild Canada geese (Branta canadensis) for ABV.

30 eport the resting metabolic rate in barnacle geese (Branta leucopsis) and provide evidence for the si

31 Barnacle geese (Branta leucopsis) were tracked with solar GPS/ARG

32 and a selective vertebrate grazer (barnacle geese, Branta leucopsis).

33 Geese breeding in the Arctic have to do so in a short ti

34 Transmission of Go/Gd-like H5N1 viruses to geese by contact with infected geese resulted in infecti

35 materia and Polysticta species), and emperor geese (Chen canagica)), ages (adults higher than juvenil

36 eocoastal peoples used such tools to capture geese, cormorants, and other birds, along with marine ma

37 The Hawaiian lineage of Canada geese diverged more dramatically, splitting into at leas

38 en following a large-scale exodus of nesting geese from the eider colony.

39 us (aMPV) recently isolated from wild Canada geese (goose 15a/01) in the United States, together with

40 Three other aMPV isolates from Canada geese had similarly large G genes, whereas analysis of r

41 In some areas the overabundance of geese has led to a drastic reduction in available forage

42 se actions, the increasing abundance of snow geese has since induced a state of satiation in harvest

43 and destructive foraging behaviours of snow geese have created a trophic cascade that reduces (sub-)

44 of the devastating trophic cascade that snow geese have triggered.

45 of A/goose/Guangdong/1/1996 (H5N1) in farmed geese in southern China, highly pathogenic H5N1 avian in

46 dnaviruses were cloned from exotic ducks and geese, including the Chiloe wigeon, mandarin duck, puna

47 sed by apparent competition with lesser snow geese, mediated by shared predators.

48 d a previously unknown radiation of Hawaiian geese, of which only one representative remains alive (t

49 ng of migratory movements of Arctic breeding geese on different flyways to examine whether flyways di

50 tes or swabs were collected from wild ducks, geese, owls, sparrows, swallows, and starlings and from

51 l migration like that of its living duck and geese relatives, or it may have been a year-round reside

52 N1 viruses to geese by contact with infected geese resulted in infection of all birds but limited sig

53 whereas the two Nearctic lineages of Canada geese share a primitive plumage pattern.

54 PV RNA was detected in samples examined from geese, sparrows, and starlings.

55 Historically, juvenile snow geese suffered from density-related degradation of their

56 However, geese tend to adopt a partial capital breeding strategy

57 rabundant breeding population of lesser snow geese that has dramatically damaged the ecosystem, with

58 March 1999, this monitoring system detected geese that were serologically positive for H5N1 avian in

59 ith the aim of controlling overabundant snow geese, the Conservation Order amendment to the Internati

60 Transmission from infected geese to chickens occurred only by fecal contact, wherea

61 c conditions at subsequent stopovers enables geese to closely track the green wave.

62 The green wave hypothesis posits that geese track a successively delayed spring flush of plant

63 We find that geese track neither the onset of spring nor the peak in

64 s on cause-specific mortality in lesser snow geese using multistate capture-reencounter methods.

65 ks, Mallard ducks, Muscovy ducks, and Embden geese with 10(6) 50% egg infective doses of the A/Anhui/