ライフサイエンスコーパス: heterospecific

1 also provide information to another species (heterospecific).

2 s own species is favoured in the presence of heterospecifics.

3 lant species were limited by conspecifics or heterospecifics.

4 kely to switch from choosing conspecifics to heterospecifics.

5 he species that better discriminated against heterospecifics.

6 Conspecific and heterospecific aboveground and belowground herbivores of

7 ease conspecific adult feeding, but decrease heterospecific aboveground insect feeding and abundance.

8 cialist beetle Bikasha collaris and multiple heterospecific aboveground species interact to determine

9 predicted that foragers could eavesdrop upon heterospecific alarm pheromones, and would detect and av

10 for olfactory eavesdropping and avoidance of heterospecific alarm signals, alarm pheromones, at food

11 Recognition of heterospecific alarm vocalizations is an essential compo

12 ion and male reproductive phenotypes between heterospecific and conspecific Y chromosomes.

13 ked their developmental fate in conspecific, heterospecific, and mixed-species crosses.

14 Consequently, females typically avoid heterospecifics as mates.

15 en sequences are also capable of controlling heterospecific association.

16 -helical pairings indicated a preference for heterospecific associations.

17 We suggest that heterospecific cache pilferage represents an especially

18 age and experience are important factors in heterospecific call recognition by bonnet macaques.

19 ing discrimination from background noise and heterospecific calls.

20 hat extracellular DNA, both homospecific and heterospecific, can also serve as the sole source of car

21 r medial amygdala of male mice, whereas most heterospecific chemosignals (e.g.: hamster vaginal fluid

22 ne responses to conspecific chemosignals and heterospecific chemosignals were characteristically diff

23 appropriately to subtle variations of these heterospecific "chick-a-dee" alarm calls, thereby eviden

24 Here we propose that asynapsis of heterospecific chromosomes in meiotic prophase provides

25 and fused each fragment to one subunit of a heterospecific coiled coil.

26 major constituent was allelopathic against a heterospecific competitor, Poa pratensis, but not agains

27 Cre and Dre are heterospecific: Cre did not catalyze recombination at ro

28 dence (CNDD), but there was little effect of heterospecific density.

29 imers can be produced upon the addition of a heterospecific DNA cross-linking strand.

30 Contrary to expectation, heterospecific (donor) alleles of TRDLs were favored as

31 lowing copulation with either conspecific or heterospecific (Drosophila arizonae) males at three time

32 both sexual imprinting and learning to avoid heterospecifics during adulthood promote assortative mat

33 ould prevent sperm from pointlessly tracking heterospecific eggs.

34 ion factors to prevent proper recognition of heterospecific enhancers.

35 erature) and biological (density of con- and heterospecifics) factors.

36 ecific female than when in the presence of a heterospecific female.

37 trated male mate choice for conspecific over heterospecific females also is revealed in sperm product

38 choice experiments, N. inaurata males chose heterospecific females in 30% of trials.

39 om T. castaneum are mated to conspecific and heterospecific females, we do not observe a significant

40 ch will also maintain the potential for rare heterospecific fertilisation that typically cause rapid

41 rs and to us, to distinguish conspecific and heterospecific fish.

42 ve (i.e. parasitoid attacks conspecifics and heterospecifics for the production of males) autoparasit

43 or discriminating close from distant kin and heterospecifics from conspecifics might be one's own sel

44 xing" strategies, which rely on a variety of heterospecific FRT-site variants (F').

45 In contrast, heterospecific fruit set of Q. gambelii was the same at

46 In three of four cases, heterospecific fruit set was significantly reduced compa

47 Solanum habrochaites) co-introgressed into a heterospecific genetic background (Solanum lycopersicum)

48 lts from particular interactions between the heterospecific genomes and suggests that substantial gen

49 Finally, heterospecific grafting experiments demonstrated that T.

50 Using a heterotopic, heterospecific grafting strategy we demonstrate that rho

51 ) when they were in the presence of either a heterospecific, gynogenetic female (Poecilia formosa, Am

52 here and phyllosphere microbiota of con- and heterospecific hosts from four species were independentl

53 as similar compared with the flank odor of a heterospecific individual.

54 osses, suggesting that positive and negative heterospecific interactions affect introgression rates i

55 However, when conspecific or heterospecific juveniles were present, the effects of re

56 uit) and social cues (conspecific juveniles, heterospecific juveniles, no juveniles) for a cactus-fee

57 tic incompatibility between a single pair of heterospecific loci.

58 -type loxP site at one end and by a modified heterospecific lox site (loxM3) at the other.

59 ing occurs only with a DNA vector carrying a heterospecific lox site in which the spacer region has b

60 Such heterospecific lox sites also allow Cre to specifically

61 By placing different heterospecific lox sites at different genomic locations,

62 Thus, in the same cell, heterospecific lox sites can be used independently at mu

63 The strategy utilizes a pair of heterospecific lox sites engineered both into the genome

64 However, recombination between cis-linked heterospecific lox sites limits the use of Cre- mediated

65 he cassette carries a marker gene bounded by heterospecific lox sites that cannot recombine with each

66 The incompatibility of the heterospecific lox sites used for the recombinase-mediat

67 t lox sites having an altered spacer region (heterospecific lox sites) are not proficient for Cre-med

68 CsA suppressed the heterospecific lymphocytotoxic antibody response and inh

69 ratus) to saline, conspecific male odors, or heterospecific (M. brandti) male odors and quantified th

70 estigated conspecific male odors longer than heterospecific male odors.

71 a female mates with both a conspecific and a heterospecific male, the conspecific sperm fertilize the

72 alities, female webs were often inhabited by heterospecific males that sometimes outnumbered conspeci

73 e spadefoot toads were more likely to choose heterospecific males when exposed to environmental condi

74 n nearby allopatric populations to mate with heterospecific males.

75 nces in response to odors of conspecific and heterospecific males.

76 While heterospecific mating in the laboratory never produced o

77 ecological and evolutionary consequences of heterospecific mating interactions in Nephila that may b

78 Though not uncommon in other animals, heterospecific mating is rarely reported in arachnids.

79 In addition, we prove that heterospecific mating is the only option for European S.

80 To avoid heterospecific mating, males respond to female-produced

81 pecies in the effect of conspecific, but not heterospecific, neighbors on survival, and we found a si

82 responses of each species to conspecific vs heterospecific neighbours in a common garden.

83 er the effects of larger conspecific and all heterospecific neighbours.

84 ge between mycelia and recombination between heterospecific nuclei may be of more importance to funga

85 pecific odors than when they were exposed to heterospecific odors.

86 f multiple paternity or maternity), or among heterospecifics or unrelated conspecifics (brood parasit

87 We propose the heterospecific pairing of homologous chromosomes as a pr

88 les develop at the expense of conspecific or heterospecific parasitoid prepupae.

89 Of special interest are heterospecific peptide pairs that participate in mutuall

90 Birds also learned heterospecific phrases, confirming previous evidence tha

91 ns and assessed their comparative success at heterospecific pilfering in a naturalistic laboratory se

92 e linked to asymmetrical competition through heterospecific pollen transfer.

93 ly in self-incompatible species that require heterospecific pollen.

94 Manual heterospecific pollination by S. admonitor resulted in a

95 however, we estimate that the ratio of self: heterospecific pollination in open-pollinated flowers wa

96 Despite the efficacy of heterospecific pollination, the contribution of S. admon

97 nts to isolate eight peptides that form four heterospecific PPIs when combined.

98 process, we have derived peptides that form heterospecific PPIs when combined.

99 easingly large and therefore complex sets of heterospecific PPIs with a wide range of potential downs

100 Thus, a heterospecific predator (cat collar) stimulus, which eli

101 of adult rats to a conspecific juvenile or a heterospecific predator odour leads to increases in Egr-

102 e of conspecific tree seedlings (relative to heterospecific seedlings) is reduced when grown in the p

103 uitment of conspecific seedlings relative to heterospecific seedlings.

104 ial neural representation of conspecific and heterospecific signals involves both changes in mean act

105 ng responses toward conspecific signals over heterospecific signals, and toward particular features o

106 ommunicate effectively against a backdrop of heterospecific signals.

107 e conserved gene order (synteny) revealed by heterospecific SNP maps is in concordance with that of t

108 Due to their density, the heterospecific SNPs allow fine-grained comparisons, incl

109 ay 6.0 and cataloged 85,473 uniquely mapping heterospecific SNPs.

110 st that the presence of both conspecific and heterospecific social cues can disrupt responses of indi

111 rained to discriminate among conspecific and heterospecific song segments in a go/no-go operant task.

112 d the discrimination between conspecific and heterospecific songs but not among conspecific songs.

113 lings discriminated among novel starling and heterospecific songs, indicating an open-ended category

114 erleaved sequences with other conspecific or heterospecific songs.

115 ighbors of the same (conspecific) and other (heterospecific) species can influence a species' relativ

116 ith conspecifics from signals used by other (heterospecific) species relevant to their social behavio

117 Heterospecific sperm fertilize fewer eggs after these do

118 m aggregate more often with conspecific than heterospecific sperm, suggesting that individual sperm c

119 ounded by docile individuals were invaded by heterospecific spiders more quickly, grew more rapidly i

120 erformance under two conditions: (1) foreign heterospecific spiders present and (2) foreign spiders r

121 conspecific stimuli (socially relevant) and heterospecific stimuli (not socially relevant but servin

122 dual at HZ was highly fecund, and had higher heterospecific than conspecific fruit set; slight introg

123 mately twice as many eggs in the presence of heterospecifics than alone or in the presence of conspec

124 he role of learning in the discrimination of heterospecific vocalizations by wild bonnet macaques (Ma

125 perimental evidence that the interception of heterospecific vocalizations can mediate interactions be

126 ion of communication sounds (conspecific and heterospecific vocalizations), whereas GABAB receptor an

127 presented with a variety of conspecific and heterospecific vocalizations, white noise, and tones.

128 When heterospecifics were present, colonies founded by docile

129 encountered both neighbours (conspecific and heterospecific) with high and even frequency.

130 n Drosophila, we find that the presence of a heterospecific Y chromosome has no significant effect on

131 Genes down-regulated in males with heterospecific Y chromosomes are significantly biased to

132 Here we address the contribution of 'heterospecific Y chromosomes' to fertility in hybrid mal