ライフサイエンスコーパス: hydraulic conductance

1 he plastidic SlFRK3 in xylem development and hydraulic conductance.

2 literation of the dentinal tubules to reduce hydraulic conductance.

3 to hydraulic failure should have low maximum hydraulic conductance.

4 osynthetic rate was not associated with leaf hydraulic conductance.

5 - 9.3% and occurred beyond 88% loss of xylem hydraulic conductance.

6 -specific photosynthetic rate, and soil-leaf hydraulic conductance.

7 interpretation of measured stomatal and leaf hydraulic conductances.

8 nerability curves (VCs) describe the loss of hydraulic conductance against increasing xylem tension,

9 A combination of regulation of stomatal and hydraulic conductance and access to belowground water re

10 nces in key hydraulic traits, including leaf hydraulic conductance and capacitance, as well as the ki

11 GS was an indirect effect of decreased leaf hydraulic conductance and increased leaf shading.

12 s results in a significant reduction in leaf hydraulic conductance and leaf gas exchange.

13 howed a role of SSWU in the recovery of leaf hydraulic conductance and revealed that SSWU is sensitiv

14 Perianth hydraulic conductance and the amount of xylem to transpi

15 e dynamic patterns of leaf ABA levels, plant hydraulic conductance and the point of failure in the so

16 f drying, the control plants recovered their hydraulic conductance and their transpiration rates fast

17 implosion strength, reduced conduit-specific hydraulic conductance, and compromised leaf-specific xyl

18 tential, stomatal conductance, loss of xylem hydraulic conductance, and electrolyte leakage were also

19 stigated the role of xylem cavitation, plant hydraulic conductance, and root pressure in the response

20 orative demand, and partly to differences in hydraulic conductance arising from the need to balance m

21 cient to explain the rise in synovial lining hydraulic conductance at 25 cmH2O when taken in conjunct

22 water potential, leaf gas exchange, and root hydraulic conductance attested that, under irrigation, M

23 lly, the model parameter representing radial hydraulic conductance between phloem and xylem showed a

24 n 6-year-old branches (pressure that reduces hydraulic conductance by 50% = 1.6-2.4 MPa), whereas the

25 h of the current year (pressure that reduces hydraulic conductance by 50% = 3.8 MPa).

26 contrasting succulent systems and associated hydraulic conductance components should be compared in t

27 d roots rapidly, and both storage carbon and hydraulic conductance decrease significantly within a ye

28 Reversible recovery of hydraulic conductance, desiccation-tolerant seeds, or rh

29 Soil-leaf hydraulic conductance determines canopy-atmosphere coupl

30 ve conductances and vulnerability to loss in hydraulic conductance dictated stomatal sensitivity and

31 plays a major role in the reduction of plant hydraulic conductance during drought, and (b) that rice

32 The leaf hydraulic conductance expressed on a leaf area basis was

33 ls (aquaporins), decreased LP and the radial hydraulic conductance for the stele (L(R, S)) of the dis

34 controlled by the reduction in outside-xylem hydraulic conductance, for example the reorganization of

35 s may provide mechanisms that could decouple hydraulic conductance from other plant functions.

36 a greater conduit-specific and leaf-specific hydraulic conductance in association with increased vess

37 evels associated with incipient loss of leaf hydraulic conductance in four species.

38 ulics, in general, and extravascular, radial hydraulic conductance in leaves (K(leaf)), in particular

39 We believe that the increase in root hydraulic conductance in one part causes a decline of wa

40 segmentation hypothesis (HSH) proposes that hydraulic conductance in shorter lived, 'expendable' org

41 Additionally, we asked whether the maximum hydraulic conductance in the soil-plant continuum k(max)

42 lastic lipids on dynamic surface tension and hydraulic conductance in xylem.

43 , which at low pressures represents synovial hydraulic conductance, increased from a control of 0.90

44 or loss point and stem P50 (tension at which hydraulic conductance is at 50% of maximum) were uncorre

45 ses suggest that the effect of variable leaf hydraulic conductance is negligible.

46 Hydraulic conductance is recognized as a major determina

47 declines of stomatal conductance g(s) , and hydraulic conductance K(leaf) , including xylem and outs

48 ce, and importance value, and quantified the hydraulic conductance (K(h) ) of above-ground and below-

49 Distal leaves had higher leaf hydraulic conductance (K(leaf) ) and g(s) compared to ba

50 We hypothesized that the decline of leaf hydraulic conductance (K(leaf) ) in response to dehydrat

51 nvestigated the temperature response of leaf hydraulic conductance (K(leaf) ), stomatal (g(s) ) and m

52 The leaf hydraulic conductance (K(leaf) ), stomatal conductance (

53 The leaf hydraulic conductance (K(leaf)) represents the capacity

54 Leaf hydraulic conductance (K(leaf)) was measured from the re

55 Leaf hydraulic conductance (K(Leaf)), carbon isotope discrimi

56 uld also lead to higher leaf capacitance and hydraulic conductance (K(leaf)).

57 e xylem would cause a strong decline of leaf hydraulic conductance (K(leaf)).

58 may depend on higher vein density (D(v)) and hydraulic conductance (K(leaf)).

59 We measured whole-plant hydraulic conductance (K(p)), osmolality, concentrations

60 dlings increased four-fold in absolute shoot hydraulic conductance (K(shoot) ) and declined by half i

61 ed traits such as stomatal regulation, shoot hydraulic conductance (K(shoot) ) and stem xylem embolis

62 eedlings had higher leaf area-specific shoot hydraulic conductance (K(shoot-L) ), and stomatal conduc

63 imate predicts drought-induced loss of plant hydraulic conductance (k), canopy G, carbon assimilation

64 branching to predict metabolic scaling from hydraulic conductance, K, (a metabolism proxy) and tree

65 Leaf hydraulic conductance (Kleaf ) quantifies the capacity o

66 rability, leaf water potential (Psil ), leaf hydraulic conductance (Kleaf ), photosynthesis (A), stom

67 diterranean-type ecosystem by measuring leaf hydraulic conductance (Kleaf) and stem hydraulic conduct

68 ering the mesophyll-increase the leaf radial hydraulic conductance (Kleaf) by acidifying the xylem sa

69 During drought-induced dehydration, the leaf hydraulic conductance (Kleaf) declines, which contribute

70 ferent methods consistently showed that leaf hydraulic conductance (Kleaf) was down-regulated by exog

71 Declines in leaf hydraulic conductance (Kleaf) with increasing water stre

72 to water stress (50% reduction in whole-leaf hydraulic conductance [kleaf] at -0.2 to -0.8 MPa).

73 al variation across species on outside-xylem hydraulic conductance (Kox).

74 plants lost 50% (P50 x RR ) of maximum leaf hydraulic conductance (Ksat ), and compared this trait w

75 Decline of leaf xylem hydraulic conductance (Kx ) during dehydration was drive

76 chilling-sensitive plants are chilled, root hydraulic conductance (L(o)) declines precipitously; L(o

77 matal conductance, transpiration rate, plant hydraulic conductance, leaf water potential, osmotic pre

78 Drought-induced changes in root hydraulic conductance (LP) and mercury-sensitive water t

79 promoted significant reduction in the dentin hydraulic conductance, mainly with higher energy densiti

80 ewed from this perspective, the elevation of hydraulic conductance marks a major milestone in the evo

81 of water to conserve soil moisture (reduced hydraulic conductance, narrow metaxylem vessels), and im

82 e have performed computer simulations of the hydraulic conductance of a branched transport system.

83 p a model based on electroviscosity in which hydraulic conductance of an electrically charged porous

84 aim of the present study is to evaluate the hydraulic conductance of bovine root dentin after irradi

85 Hydraulic conductance of native osteochondral tissue and

86 The study hypothesis was that hydraulic conductance of osteochondral tissue and subcho

87 e, nutrient content, respiration, and radial hydraulic conductance of root tissue.

88 In perfusion experiments, the hydraulic conductance of stem segments ( ) responds to c

89 t kappa, which is a measure of the intrinsic hydraulic conductance of the gel, decreased by an order

90 chondroitinase ABC (5 joints) increased the hydraulic conductance of the lining by 2.3 times (contro

91 s, i.e. below yield pressure, represents the hydraulic conductance of the lining, i.e. 1/resistance.

92 hydraulic system showed that a reduction of hydraulic conductance of the mesophyll pathways outside

93 During joint loading, increased hydraulic conductance of the osteochondral tissue and su

94 al, dominated by the large loss (10-fold) of hydraulic conductance of the outside-xylem tissue, is no

95 thological values (> 9 cmH2O) by saline, the hydraulic conductance of the synovial lining increases m

96 leaves, this approach provides access to the hydraulic conductance of the whole leaf, xylem, and outs

97 As a result, the hydraulic conductance of the whole plant was unchanged.

98 cores were perfusion-tested to determine the hydraulic conductance, or ease of fluid flow, in their n

99 The C(4) species had lower hydraulic conductance outside xylem (K(ox) ) and K(leaf)

100 il dropped and stayed below 50% loss of leaf hydraulic conductance (P(5)(0)) early in the day during

101 measuring the pressure inducing 50% loss of hydraulic conductance (P50) in stems of 26 species, main

102 Variation and dynamics in hydraulic conductance, particularly within leaves, may c

103 Changes in plant hydraulic conductance partly counteracted those of trans

104 at experimental measurements of stomatal and hydraulic conductances should be affected directly by ch

105 Consequently, hydraulic conductance, stomatal conductance, and assimil

106 tely veined leaves declined strongly in leaf hydraulic conductance, stomatal conductance, and photosy

107 e, leaf diffusive conductance, and soil-leaf hydraulic conductance that were associated with cavitati

108 may be recovered through SSWU, and that the hydraulic conductance to SSWU (K(surf) ) declines with d

109 uctance, and compromised leaf-specific xylem hydraulic conductance under moderate drought.

110 Leaf hydraulic conductance was also relatively low for both s

111 The dentin hydraulic conductance was evaluated at four time periods

112 is weakly expressed in wild-type plants, the hydraulic conductance was higher in the PIP2;5 OE lines

113 th a high-pressure flowmeter, and whole-stem hydraulic conductance was measured by a vacuum chamber m

114 Saturated root hydraulic conductance was measured with a high-pressure

115 r transport system in plants should maximize hydraulic conductance (which is proportional to photosyn

116 vitation and caused a complete loss of xylem hydraulic conductance within a very short time.