ライフサイエンスコーパス: allometry

1 dy mass, whilst length shows strong negative allometry.

2 dely but independently of the toughness-mass allometry.

3 size in all the colonies showing a negative allometry.

4 e form and parameter values of variance-mass allometry.

5 erties of river systems, including metabolic allometry.

6 al posture, or vice versa, based on skeletal allometry.

7 h each order, exhibiting a specific negative allometry.

8 behaviours interact in shaping reproductive allometry.

9 or scales with its body size is known as an allometry.

10 variation in absolute size on the resulting allometry.

11 this species absent the potential impact of allometry.

12 ity; and (5) genetic regulation of appendage allometry.

13 les, systolic blood pressure and adult organ allometry.

14 origin of alternative phenotypes and complex allometries.

15 ctions are most consistent with our observed allometries.

16 lutionary transformations in encephalization allometries.

17 hat they almost universally exhibit positive allometries.

18 Metabolic allometry, a common pattern in nature, is a close to 3/4

19 1 (RSA1) associated with differences in root allometry, a highly plastic trait capturing the distribu

20 Taylor's law and density-mass allometry accurately predicted the form and parameter va

21 efers to the changes in leaf shape and size (allometry) along stems.

22 Moreover, allometry analyses indicated that constitutive developme

23 spertilionid bats: (i) mass-signal frequency allometry and (ii) emitter-limited (maximum gape) signal

24 general model, based on first principles of allometry and biochemical kinetics, that predicts the ti

25 aled transpiration with measurements of tree allometry and delta(13) C of leaf soluble sugars to esti

26 morphological change--horn location, shape, allometry and dimorphism--and we illustrate how the deve

27 elative to total body size are called static allometry and have enchanted biologists for centuries, y

28 a, adhesive pad area showed extreme positive allometry and scaled with weight, implying a 200-fold in

29 We propose to integrate the notion of allometry and the classical reaction norm into a composi

30 neous and disordered kinetics, organ growth (allometry), and population genetics.

31 isometry, whilst length scales with negative allometry, and close to elastic similarity in the tibiot

32 s and the evolution of horn location, shape, allometry, and dimorphism.

33 ain evolution within its basic developmental allometry, and provide an empirical basis to recognize e

34 le toward understanding the observed spindle allometry, and the universal scaling relationship betwee

35 We modeled leaf growth and allometry as function valued traits (FVT), and examined

36 e, control for the confounds associated with allometry as well as growth differences between the brai

37 We identified leaf shape (allometry) as a genetic module independent of length and

38 model that can quantify differences in leaf allometry between Antirrhinum (snapdragon) species, incl

39 uration, and an empirically derived positive allometry between reproductive potential and size.

40 ckdown of dsx dramatically altered male horn allometry by massively reducing horn development in larg

41 In insects, static allometry can be divided into at least two processes: (1

42 growth rates of different biological organs (allometry) can be described by a similar approach.

43 of 485 mg, determined from the MLP-corrected allometry Cl/F, was well within the dose range of 400 mg

44 e-generated P cells increasing with positive allometry compared with the earlier-generated M cells.

45 Density-mass allometry (DMA) asserts that the mean population density

46 feration associated with regulation of plant allometry during the stress response.

47 h depends on only the crown area-to-diameter allometry exponent: a well-conserved value across tropic

48 ing, 'Size in Development: Growth, Shape and Allometry' focused on the molecular and cellular mechani

49 irst empirical confirmation of variance-mass allometry for any animal community.

50 reproduction and explains why interspecific allometries have consistently lower exponents than intra

51 tic changes in body shape and its associated allometry have been poorly understood partly due to the

52 id growth kinetics can produce nearly linear allometries in both the arithmetic and logarithmic domai

53 ative to smaller taxa may be due to positive allometry in skull size with body mass in ceratopsids, w

54 relationship is one of many scaling laws, or allometries, in ecology and biology that have received m

55 functions of growth curves and developmental allometry into the estimation process of genetic mapping

56 Perhaps the most central biological allometry is how metabolic rate scales with body size.

57 on pathogen transmission, host mass gain and allometry it is shown how investing in tolerance to a no

58 e, made possible by recently developed shrub allometry models.

59 Here, we use an optimal foraging model and allometries of foraging variables to predict the structu

60 ionary game theoretical model with empirical allometries of growth and nutrient uptake shows that the

61 level, a total 122 QTNs were associated with allometries of kidney, spleen and liver weights to body

62 Here, we study the allometry of adhesive pad area in 225 climbing animal sp

63 the -1/4 power law classically inferred from allometry of animal metabolic rates.

64 Here we review the evolutionary allometry of exaggerated sexual traits (for example, ant

65 ometries, we find that the extreme wing area allometry of hummingbirds is likely an adaptation to mai

66 ution to those interested in theories of the allometry of metabolic rates.

67 Experiments demonstrate allometry of mitotic spindles and a universal scaling re

68 ral botanical data sets with measures of the allometry of morphological traits.

69 al scales is fundamental to the detection of allometry of movement and should be given more attention

70 RSA1 genes in Columbia-0 phenocopy the root allometry of other natural variants.

71 count the potentially confounding effects of allometry on quantitative craniodental characters.

72 s or how it might relate to other aspects of allometry or other developmental transitions.

73 Several patterns of brain allometry previously observed in mammals have been found

74 f principles that include site-specific tree allometries, random placement of trees, competition for

75 that embryonic metabolism followed intrinsic allometry rules among 49 songbird species from temperate

76 Joint static allometry scaling equation as sub-model is nested within

77 l inference of genomic imprinting underlying allometry scaling in animals.

78 of animal biology, including metamorphosis, allometry, size-dependent alternative pathways of gene e

79 Maximum gape also scales with positive allometry (SL(1.20)), indicating that larger neonates ar

80 jaw-closing musculature scales with positive allometry (SL(2.72)) indicating that muscle growth outpa

81 ty correlates with overall variation in leaf allometry, so species with smaller, rounder leaves produ

82 Biological allometries, such as metabolic scaling, have been hypoth

83 e, coupled with diurnal root pressure and an allometry that allows substantial leaf area to be suppor

84 ition to a remarkably static basal Carnivora allometry that characterizes much of the suborder Felifo

85 ans scale with body size, a process known as allometry that has been studied extensively in a range o

86 lly diverse sample reflect spatially optimal allometry that minimizes investment in the allocation of

87 ed on principles of biochemical kinetics and allometry, that characterizes the effects of temperature

88 atial mean population density); density-mass allometry (the spatial mean population density was a pow

89 nction of mean body mass); and variance-mass allometry (the spatial variance in population density wa

90 contexts, reducing vocal tract and laryngeal allometry thereby exaggerating apparent body size.

91 urns a highly derived sigmoid horn body size allometry to its presumed ancestral, linear state.

92 We call this relationship "variance-mass allometry" (VMA).

93 However, simulated reproductive allometry was a poor predictor of that observed.

94 The fact that the negative allometry was more pronounced in RNA viruses than in DNA

95 During this period, allometry was revealed at multiple temporal intervals (h

96 By comparing inter- and intraspecific allometries, we find that the extreme wing area allometr

97 Component fluxes were explained more by allometry, while partitioning to components was related

98 es in our understanding of the mechanisms of allometry will come through the integrated study of whol

99 tarsometatarsus width shows strong positive allometry with body mass, whilst length shows strong neg

100 by comparison of maximum somatic growth rate allometry with groups of known metabolism.

101 the LP-pulvinar complex scaled with positive allometry with respect to brain volume across all specie