ライフサイエンスコーパス: life history strategy

1 ogy as one functional trait within a plant's life history strategy.

2 ionary causes of this surprising and extreme life history strategy.

3 which facilitates an adaptive shift in their life-history strategy.

4 of fitness through which selection acts upon life-history strategy.

5 ut smaller offspring, which is a maladaptive life-history strategy.

6 that are thought to underlie differences in life-history strategy.

7 showed major changes in the distribution and life-history strategy.

8 turally acidic seawater vent system to their life history strategies.

9 heir tissue 15N isotope values and published life history strategies.

10 ness trade-offs involved in the evolution of life-history strategies.

11 pecies, depending on complex interactions of life-history strategies.

12 w to test two predictions regarding parasite life-history strategies.

13 nity vary between individuals with different life-history strategies.

14 cal drivers of geographic variation in avian life-history strategies.

15 the evolution of phenotypes with alternative life-history strategies.

16 at each of these stages has shaped microbial life-history strategies.

17 for individuals and groups to adopt a slower life history strategy, a greater focus on the future (vs

18 The identification of patterns in life-history strategies across the tree of life is essen

19 ow theory because they commonly exhibit slow life history strategies and produce larger, but fewer, e

20 x interaction between an individual's needs, life history strategies and the varying local environmen

21 aborative work that takes into account viral life history, strategy and evolution, and host genetics,

22 e fact that different species have different life-history strategies and variables, such as lifespan,

23 olution is influenced by the intersection of life-history strategy and climatic niches into which pla

24 se to these perturbations largely depends on life-history strategy and density regulation.

25 plant species that differ in mating system, life-history strategy and growth form.

26 has implications for dinosaurian embryology, life history strategies, and survivorship across the Cre

27 istory strategy, large species with periodic life history strategy, and for all trophic levels except

28 Quantifying among-individual variation in life-history strategies, and associated variation in rep

29 parasitic angiosperms in form and structure, life-history strategies, and plastid genomes, little is

30 to unpredictability, the adoption of a fast life-history strategy, and dysregulated-eating behaviors

31 This shift in life history strategy appears to be adaptive, because fi

32 tude environments, calling into question the life history strategy approach used, and that it is inco

33 Life history strategies are being displayed by a domesti

34 to elevated pCO2 in seaweeds with different life-history strategies are scarce.

35 Our findings have similarities with how life-history strategies are structured in mammals, birds

36 ral ecology-specific adaptations, apart from life-history strategies, are responsible for the behavio

37 ns in eggs, foraging guild, nor to a species life history strategy as characterized along the precoci

38 itional evidence for this shift in bacterial life history strategies because nutrient additions decre

39 response across aphid morphs that differ in life-history strategy but are genetically identical.

40 edes Basin during 2011, indicating that both life- history strategies can coexist.

41 lts demonstrate that changes in reproductive life-history strategy can stimulate diversification.

42 rasite specialism or generalism based on the life-history strategies employed by hosts, and investiga

43 However, the main life-history strategies existing in a set of taxa are of

44 l models make different predictions on which life history strategies facilitate growth of small popul

45 reveals a hitherto unrealized flexibility in life-history strategies for these species and underscore

46 Moa showed the exaggerated K-selected life-history strategy formerly common in the New Zealand

47 tistical analysis probably would find slower life history strategy, greater focus on the future, and

48 How the costs of immunity vary across life-history strategies has yet to be considered.

49 Badgers exhibit a slow life-history strategy, having high rates of adult surviv

50 Red droppers followed a risk-averse life-history strategy (high late reproduction), red nond

51 This diversity of life-history strategies illustrates that there are many

52 used in biocontrol, depends on a variety of life history strategies in conflict with those of their

53 dependence of physiological, behavioral, and life history strategies in the evolution of apes and hum

54 palaeoecological implications of changes in life history strategies in the therapsid forerunners of

55 ate that dispersal in early life might shape life history strategies in wild populations.

56 Selection for alternate life-history strategies in natural versus human-associat

57 Melanin-based colouration varies with life-history strategies in ruffs and other species, thus

58 We demonstrate that a fast life-history strategy, in turn, was associated with dysr

59 gative effects on the persistence of several life-history strategies, including early spring flight s

60 In a virus, a life history strategy is largely manifested in its repli

61 We show that 55% of the variation in plant life-history strategies is adequately characterized usin

62 sive examination of its effects on different life-history strategies is lacking.

63 and female mode at the same time, and such a life-history strategy is adopted by most flowering plant

64 for species of all sizes having equilibrium life history strategy, large species with periodic life

65 ly validate the hypothesis that species with life history strategies linked to parental care are more

66 Species with "slow" life history strategies (long life, low fecundity) are t

67 Consequently, behaviour and life-history strategies may be as much a function of nut

68 plication of our finding for the gradient of life-history strategies observed among species and argue

69 s in autocorrelation among two major axes of life-history strategies, obtained from phylogenetically

70 axa and ecosystems, and the evolution of the life history strategies of masquerading prey.

71 Research on life history strategies of microbial symbionts is key to

72 ndings provide insight into the evolution of life history strategies of tropical birds.

73 s necessary to understanding the ecology and life history strategy of the microorganism and to develo

74 The life-history strategies of organisms are sculpted over e

75 Therefore, the life-history strategy of Ae. arabicum appears to be a bl

76 mparative approach to show that the original life-history strategy of American crocodiles is actually

77 vival differed between the sexes and whether life history strategies (often reported in wild or feral

78 ysis demonstrates the influence of long-term life-history strategies on species response to short-ter

79 s) is associated with the adoption of a fast life-history strategy, one marked by impulsivity and a f

80 to test hypotheses regarding the effects of life-history strategy, population density, average cause

81 These life-history strategies present different social organiz

82 Across salmonid species, life-history strategies range from wholly freshwater-res

83 s can select for various changes in parasite life history strategies relative to single genotype infe

84 rom desperate ecologies as possessing faster life history strategies than people from hopeful ecologi

85 Many marine fishes have life history strategies that involve ontogenetic changes

86 which this may be achieved, including viral life history strategies that result in low rates of with

87 ore, the invaders' offspring follow a unique life-history strategy that may enhance their ability to

88 ses special problems not covered by standard life history strategy theory.

89 Macroparasites have common life-history strategies to achieve this, but these gener

90 Animals must tailor their life-history strategies to suit the prevailing condition

91 n and phenology, aggregative and circumnatal life history strategies, voltinism, diapause, aestivatio

92 rtance of these timing advances for a stable life history strategy, we constructed a full life cycle

93 e species in acidic conditions is related to life history strategies where eggs are kept in protected

94 framework to quantify the variation in plant life history strategies world-wide.