ライフサイエンスコーパス: hydraulics

1 on and the role of root growth on soil-plant hydraulics.

2 orm in leaf veins critically determines leaf hydraulics.

3 vature that can be adjusted dynamically, via hydraulics.

4 t connectivity play a role in altering xylem hydraulics.

5 demonstrates the extreme limits of cellular hydraulics.

6 ongly related to changes in V(cmax) and leaf hydraulics.

7 C(4) photosynthesis should also impact plant hydraulics.

8 t connectivity and grouping and tissue-scale hydraulics.

9 the effect of conduit connectivity on xylem hydraulics.

10 the power of new approaches for probing leaf hydraulics.

11 merit of further study into glacier surface hydraulics and biological processes.

12 garding our understanding of soil structure, hydraulics and climate interaction.

13 also coincide with new modifications in leaf hydraulics and growth habit during angiosperm diversific

14 lant morphology, gas exchange, leaf and stem hydraulics and growth rates have evolved in a coordinate

15 taken into account as a key process in plant hydraulics and in estimating future effects of climate c

16 putative underlying mechanisms, such as stem hydraulics and legacies affected by leaf life span and s

17 estments in the competing xylem functions of hydraulics and mechanical support.

18 and length, but they are ultimately based on hydraulics and mechanics.

19 outlined in this paper can be used to couple hydraulics and ML models to reduce the computation time,

20 water status in ferns are regulated by leaf hydraulics and not metabolism.

21 Leaf structure, photosynthesis, hydraulics and nutrient composition were studied in 33 c

22 stomatal aperture variation and whole-system hydraulics and of the effects of PWS and nocturnal trans

23 We present the Tree Hydraulics and Optimal Resource Partitioning (THORP) mod

24 way to incorporate recent advances in plant hydraulics and optimality theory into LSMs, and an alter

25 decoupling a canonical relationship between hydraulics and photosynthesis generally observed in vasc

26 ioxide uptake requires coordination of plant hydraulics and photosynthesis.

27 on in response to feedback between rill-flow hydraulics and rill-bed roughness, and that this feedbac

28 elated to plant trait spectra, that is plant hydraulics and size and leaf economics.

29 inear and hysteretic behaviour in soil-xylem hydraulics and the need to incorporate knowledge of hydr

30 We evaluated whether introducing plant hydraulics and topographic convergence-induced soil mois

31 root distribution, plant configuration, soil hydraulics, and climatic conditions.

32 aptive hypotheses have invoked biomechanics, hydraulics, and drought tolerance as key selection press

33 nteraction among wastewater quality, reactor hydraulics, and inactivation kinetics is often neglected

34 tion in traits related to gas exchange, leaf hydraulics, and leaf construction.

35 However, the impact of wind on plant hydraulics at a global scale remains unclear.

36 conclude by proposing a new model that has a hydraulics-based penalty function that meets all seven c

37 At the leaf level, comparisons in hydraulics between cytotypes did not show a consistent p

38 Freeze-thaw events can affect plant hydraulics by inducing embolism.

39 tes before and after the flood and peak flow hydraulics calculated from surveyed floodmarks and cross

40 ptualize how pressures generated by muscular hydraulics can act as a global mechanical regulator that

41 This review examines how plant hydraulics can provide new insights into our understandi

42 and experimental observations show how soft hydraulics can regulate the size of growing tissue shell

43 We investigated crown dieback, growth, hydraulics, carbon assimilation and nonstructural carboh

44 However, it is unknown how pedicel hydraulics change developmentally in relation to xylem a

45 ions, opening up unexplored possibilities in hydraulics, coastal science, and engineering.

46 Soil and plant hydraulics constrain ecosystem productivity by setting p

47 Here, we compiled a xylem hydraulics dataset with 1,186 species-at-site combinatio

48 handle resistance mismatches in fossil plant hydraulics, focusing on Carboniferous medullosan seed pl

49 deficit), wind speed clearly affected plant hydraulics; for example, on average, species from windie

50 Leaf hydraulics, gas exchange and carbon storage in Pinus edu

51 reaching implications for inferences in leaf hydraulics, gas exchange, water use, and isotope physiol

52 oot production and elongation and whole-root hydraulics, had a bell-shaped dependency on WD, displayi

53 To determine whether stem hydraulics impact floral water use, we quantified floral

54 and models to examine the reorganization of hydraulics in closely related C(4) and C(3) grasses.

55 Coordination between stem photosynthesis and hydraulics in green-stemmed desert plants is important f

56 owards the integration of photosynthesis and hydraulics in land-surface models.

57 nonstructural carbohydrates (NSCs) and xylem hydraulics in Pinus ponderosa saplings.

58 modeling studies highlight the role of soil hydraulics in the control of water uptake in drying soil

59 orus supplementation could improve biofilter hydraulics in the field if the biofilter is severely pho

60 e measurement of water transport and related hydraulics in the soil-root system remains a challenge.

61 rins (AQPs) in the regulation of whole-plant hydraulics, in general, and extravascular, radial hydrau

62 Plant hydraulics integrated water stress along the soil-plant

63 Here we implemented a model of plant hydraulics into the Community Atmosphere Biosphere Land

64 Plant hydraulics is an essential discipline to understand and

65 Plant hydraulics is crucial for assessing the plants' capacity

66 ) the process variability induced by reactor hydraulics is negligible when compared to the one caused

67 ng, and care should be taken when performing hydraulics measurements on excised plant organs containi

68 ppears to matter considerably for whole-tree hydraulics, mechanics, photosynthesis and potentially me

69 esearch focused on cross-validation of plant hydraulics methods are discussed, as well as a proposed

70 The new hydraulics model significantly improved (~35%-45% reduct

71 We couple a minimalist plant hydraulics model with a soil moisture model and, for the

72 ng field measurements and a plant physiology-hydraulics model, TREES.

73 zation of solutes likely depends on both the hydraulics of resaturation and the dynamics of dissoluti

74 ermined by root growth and branching and the hydraulics of root cells and tissues.

75 ot access to bedrock groundwater matched the hydraulics of the experimental trees by increasing their

76 porewater concentration, resulting from the hydraulics of the resaturation process.

77 ecreasing attachment as well as changing the hydraulics of the system.

78 Current theory recognizes a role for the hydraulics of water transport as a potential determinant

79 Although much is known about the hydraulics of xylem, the hydraulic interconnectivity and

80 ssociated with mycorrhizal affiliation, leaf hydraulics or growth form.

81 This research unifies hydraulics, photosynthesis and the leaf economics spectr

82 hat aquaporin-mediated modifications of root hydraulics play a substantial role in the regulation of

83 Our results indicate that hydraulics, rather than carbon starvation, triggers tree

84 Chii Jou Chan investigates how tissue hydraulics regulates mammalian development, with a speci

85 ce for many biomes, knowledge regarding herb hydraulics remains very limited.

86 n our experiment, instabilities between flow hydraulics, sediment transport and bedrock erosion lead

87 l stomatal optimization model based on xylem hydraulics (SOX) to predict plant responses to drought.

88 and integrates different aspects related to hydraulics, stomatal responses and carbon economy under

89 ectroactive polymers (IEAPs), pneumatics and hydraulics systems, shape memory polymers (SMPs), hydrog

90 a stable host environment and the necessary hydraulics to enable floral gigantism and/or high reprod

91 Plants modify their root hydraulics to maintain water status and strategically us

92 using a model that links leaf morphology and hydraulics to photosynthesis.

93 e at the plasma membrane and influences leaf hydraulics to regulate plant responses to abiotic stress

94 The circadian clock regulates plant tissue hydraulics to synchronize water supply with environmenta

95 To link below- and above-ground hydraulics, we then measured leaf-stem vulnerability seg

96 ed formulation be imminently employed in eco-hydraulics where the interaction between flow and vegeta

97 ansport of soil gases is controlled by plant hydraulics, whether by diffusion or mass flow via transp

98 t to determine whether changes in subglacial hydraulics will limit the potential for the speedup of f

99 y-secured on a spore was achieved via sporal hydraulics with a driving force of 299.75 Torrs (21.7% w

100 ics and the need to incorporate knowledge of hydraulics within broader frameworks of plant ecological

101 d improvement in the representation of plant hydraulics within terrestrial ecosystem and biosphere mo