ライフサイエンスコーパス: ungulate

1 280 genera grouped as 'South American native ungulates'.

2 snails) and mature larvae, definitive hosts (ungulates).

3 s) or have been eradicated (e.g., introduced ungulates).

4 optera) were more abundant in the absence of ungulates.

5 ual synepitheliochorial placenta of ruminant ungulates.

6 fever phlebovirus in humans and domesticated ungulates.

7 onditions as has been reported for some wild ungulates.

8 viduals, especially in large mammals such as ungulates.

9 r the hunting strategies for their main prey-ungulates.

10 environment interactions in two well-studied ungulates.

11 ing a more diversified clade of mammals, the ungulates.

12 e greater utilization and selection by large ungulates.

13 even remotely in populations of free-ranging ungulates.

14 lids, and a variety of wild and domesticated ungulates.

15 Indeed, comparative evidence from ungulates [9] shows that interspecific variation in coun

16 ew doors to investigate seasonal patterns of ungulate accumulations in archaeological sites using non

17 t in summer when quantified as the number of ungulates acquired per wolf per day, and least during su

18 sites is influenced by extinction risk among ungulate and carnivore hosts.

19 es for the DRB genes of primates relative to ungulate and carnivore relatives.

20 llowed greater insight into the phylogeny of ungulate and murine gammaherpesviruses.

21 oad meat diet that consisted of diverse wild ungulate and small animal species.

22 Campylobacter fetus, a bacterial pathogen of ungulates and humans, is mediated in part by the presenc

23 highly contagious viral disease of even-toed ungulates and is one of the most important economic dise

24 s and other arrhythmic species, such as many ungulates and large carnivores, must function in both th

25 cting mammalian hosts, particularly in apes, ungulates, and bats.

26 sister group to a large clade of carnivores, ungulates, and cetaceans.

27 portant implications for parasites of Arctic ungulates, and hence for the welfare of Arctic peoples w

28 n the visual cortex are found in carnivores, ungulates, and primates but are not found in rodents, in

29 everal domestic sheep and goat breeds, other ungulates, and various mammal groups for sequences relat

30 Haemosporida parasites of even-toed ungulates are diverse and globally distributed, but sinc

31 from cells and bacteria, to birds, fish and ungulates, are mobile, and live in populations with cons

32 s to cetaceans, is a large African even-toed ungulate (Artiodactyla) that grazes and has a semiaquati

33 obtained in rodents (Rodentia) and even-toed ungulates (Artiodactyla).

34 s known that whales are related to even-toed ungulates (artiodactyls), but until now no artiodactyls

35 In even-toed ungulates (artiodactyls, including cattle), limbs are ad

36 -3 years have shown that mule deer and other ungulates avoid energy infrastructure; however, there re

37 ults demonstrate strong cascading effects of ungulates, both trophic and nontrophic, and support the

38 ance against herbivore feeding, particularly ungulate browsing.

39 insect pests, but can be severely damaged by ungulate browsing.

40 ons-bats are not closely related to odd-toed ungulates but instead have a more ancient origin as sist

41 (a Late Cretaceous clade related to Tertiary ungulates), but does not support Asioryctitheria (a grou

42 nfections and abortions in wild and domestic ungulates, but its impact on population dynamics is not

43 re mesonychians, a group of extinct, archaic ungulates, but molecular analyses have indicated that th

44 vy herbivore pressure by a widespread native ungulate can lead to rapid changes in small mammal assem

45 There are indications that some wild ungulates can exhibit certain forms of energy saving mec

46 Heavy herbivory by ungulates can substantially alter habitat, but the indir

47 e species, particularly large carnivores and ungulates, cannot coexist with people at fine spatial sc

48 ocessed numerous, relatively complete, small ungulate carcasses.

49 We hypothesized that for ungulates, climatic conditions close to parturition have

50 re limited by food, like those of many other ungulates, commonly include more females than males.

51 stidae' within a clade that includes archaic ungulates ('condylarths').

52 vided a cooler thermal environment for large ungulates, decreasing operative temperature up to 16 deg

53 tential to regulate wolf populations at high ungulate densities.

54 lands, grazing by large native or introduced ungulates drives ecosystem structure and function.

55 ble alternative to hunting and/or scavenging ungulates due to dental disease and/or limited prey avai

56 y weather variables known to be important to ungulate dynamics.

57 les provisioned their chicks with introduced ungulates (e.g., sheep), which were locally present in h

58 support that interactions with overabundant ungulates enhance demographic success of invaders and de

59 e protected serviceberry growing in a nearby ungulate exclosure originated both before and after wolf

60 levels, using a series of large, long-term, ungulate-exclusion plots that span a landscape-scale pro

61 rigin of at least some South American native ungulates from 'condylarths', a paraphyletic assembly of

62 analyzed for lentiviruses in the primate and ungulate groups, but no data exist for the third (feline

63 To the extent that intact ungulate guilds help to suppress populations of small an

64 ever, there remains a common perception that ungulates habituate to energy development, and thus, the

65 We find that threatened ungulates harbour a higher proportion of single-host par

66 the production of embryonic stem cells from ungulates has proved elusive.

67 of embryonic stem cells from pigs and other ungulates has proved so difficult.

68 e leading causes of death in bison and other ungulates, has not been well studied due to the lack of

69 altered species interactions resulting from ungulate herbivore overabundance as a key cause of exoti

70 sts of four treatments: total-exclusion (all ungulate herbivores), mesoherbivore-exclusion (LMH >120-

71 nt of anthrax, a disease primarily affecting ungulate herbivores.

72 Dubbed "UHURU" (Ungulate Herbivory Under Rainfall Uncertainty), this exp

73 or: birds flock, bees swarm, fish shoal, and ungulates herd.

74 Characterizing patterns of range fidelity in ungulates, however, has remained challenging because of

75 provide early examples of prime-age-focused ungulate hunting, a human predator-prey relationship tha

76 a, is a major parasite of several species of ungulates in North America.

77 ration have not previously been assessed for ungulates in the tropics.

78 ls occurred multiple times, with a switch to ungulates independently from other mammalian Plasmodium.

79 Our results show migratory behaviour in ungulates is an individually variable trait that can res

80 Spring migration in ungulates is of particular importance for conservation p

81 ins putative domains similar to those of the ungulate lentiviral Tat protein.

82 se dual tropic immunodeficiency viruses, the ungulate lentiviruses, including equine infectious anemi

83 y conserved among human, simian, feline, and ungulate lentiviruses, which indicated that these epitop

84 of the Tat (transactivator) proteins of the ungulate lentiviruses.

85 y is consistent with a relationship to other ungulate-like afrotheres (Hyracoidea, Proboscidea) but d

86 e convergences are pervasive among unrelated ungulate-like placentals.

87 t, and meat was obtained by hunting the only ungulate living on the island, a small indigenous Cyprio

88 lated and used to infer a phylogeny in which ungulate malaria parasites form a monophyletic clade wit

89 e identity and evolutionary relationships of ungulate malaria parasites, we conducted Plasmodium cytb

90 ins, thought to be restricted to the hooved (ungulate) mammals and characterized by being expressed s

91 loss of multi-host parasites from threatened ungulates may be explained by decreased cross-species co

92 ment affects migratory patterns, and whether ungulate migration is sufficiently plastic to compensate

93 Ungulate migrations generally occur along traditional ro

94 n study for 6 y in a forest where the native ungulate Odocoileus virginianus (white-tailed deer) is o

95 The effect of ungulates on arthropods was mediated by herbaceous veget

96 We examined the effects of ungulates on taxa (plants, arthropods, and an insectivor

97 e associated with predation risk for African ungulates - on herbivore habitat use and (ii) establish

98 Nonprimate (ungulate or feline) lentiviruses might provide safer alt

99 eliscine 'hyopsodontid' 'condylarths' (early ungulates or hoofed mammals) and extant Macroscelidea.

100 carnivores (order Carnivora) and terrestrial ungulates (orders Perissodactyla + Cetartiodactyla minus

101 ll measured serviceberry stems accessible to ungulates originated since wolf reintroduction, while pr

102 Although also characteristic of ungulate orthologs, such shuttling is not conserved amon

103 lengths and turning angles in a hypothetical ungulate population with contrasting population sizes an

104 ions, which are well recognized to influence ungulate productivity, and provided a basis for comparin

105 phenomys), lagomorphs (Mimotona) and archaic ungulates (Protungulatum and Oxyprimus) strongly support

106 Ungulate responses were measured over four years, which

107 in a dataset of ten large samples of extant ungulates resulting from well-known mass mortality event

108 s displayed by extinct South American native ungulates (SANUs) confounded both Charles Darwin, who fi

109 by the trophoblast layer of the placentas of ungulate species and are inactive members of the asparti

110 icted to embryonic trophectoderm of ruminant ungulate species for a few days in early pregnancy.

111 resulting in skewed sex-ratios, and for many ungulate species this strategy is sustainable.

112 ement and conservation of muskoxen and other ungulate species with similar life-histories.

113 oss a large number of carnivore, primate and ungulate species, but empirical data on carnivore macrop

114 rative data from wild primate, carnivore and ungulate species.

115 se discoveries suggest that sociality, a key ungulate strategy to reduce predation-related mortality,

116 Comparison with other ungulate studies indicates that positive associations be

117 ate-predator (PDCP) interactions on neonatal ungulate survival by comparing spatial and temporal fluc

118 Among mountain ungulates, survival, a key determinant of demographic pe

119 ation in characterizing risk using carnivore-ungulate systems as a case study.

120 of the Late Quaternary South American native ungulate taxa Toxodon (Notoungulata) and Macrauchenia (L

121 ly contagious viral disease of cloven-hoofed ungulates that can lead to severe losses in the livestoc

122 itude use and activity budgets of a mountain ungulate, the Alpine chamois (Rupicapra rupicapra).

123 For each ungulate, we obtain approximately 90% direct sequence co

124 Site selection preferences of ungulates were quantified using resource selection funct

125 le-host parasites compared to non-threatened ungulates, which is explained by decreases in the richne

126 e visual cortex of primates, carnivores, and ungulates without assuming differences in the general vi

127 ait, adult female survival, for a threatened ungulate, woodland caribou (Rangifer tarandus caribou Gm