Night-time conductance in C3 and C4 species: do plants lose water at night?
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Wind drives nocturnal, but not diurnal, transpiration in Leucospermum conocarpodendron trees: implications for stilling on the Cape Peninsula.Nighttime stomatal conductance differs with nutrient availability in two temperate floodplain tree species.Rates of nocturnal transpiration in two evergreen temperate woodland species with differing water-use strategies.Interactive effects of elevated CO2 and drought on nocturnal water fluxes in Eucalyptus saligna.Leaf photosynthesis, respiration and stomatal conductance in six Eucalyptus species native to mesic and xeric environments growing in a common garden.Foliar water uptake: a common water acquisition strategy for plants of the redwood forest.Consequences of nocturnal water loss: a synthesis of regulating factors and implications for capacitance, embolism and use in models.The Sap Flow Dynamics and Response of Hedysarum scoparium to Environmental Factors in Semiarid Northwestern China.Nocturnal water loss in mature subalpine Eucalyptus delegatensis tall open forests and adjacent E. pauciflora woodlands.Phylogenetic and ecological patterns in nighttime transpiration among five members of the genus Rubus co-occurring in western Oregon.Inside out: efflux of carbon dioxide from leaves represents more than leaf metabolism.Nighttime stomatal conductance and transpiration in C3 and C4 plants.Seasonal variability of the parameters of the Ball-Berry model of stomatal conductance in maize (Zea mays L.) and sunflower (Helianthus annuus L.) under well-watered and water-stressed conditions.The stomatal response to evaporative demand persists at night in Ricinus communis plants with high nocturnal conductance.Foliar absorption of intercepted rainfall improves woody plant water status most during drought.Transpiration efficiency of a tropical pioneer tree (Ficus insipida) in relation to soil fertility.Populus species from diverse habitats maintain high night-time conductance under drought.Nighttime evaporative demand induces plasticity in leaf and root hydraulic traits.Ecological physiology of Pereskia guamacho, a cactus with leaves.How significant is nocturnal sap flow?Water relations and microclimate around the upper limit of a cloud forest in Maui, Hawai'i.Estimating the sensitivity of stomatal conductance to photosynthesis: a review.Differences between water permeability of astomatous and stomatous cuticular membranes: effects of air humidity in two species of contrasting drought-resistance strategy.Differential daytime and night-time stomatal behavior in plants from North American deserts.Water-use strategies of six co-existing Mediterranean woody species during a summer drought.The relationship between leaf area growth and biomass accumulation in Arabidopsis thaliana.Transition of stable isotope ratios of leaf water under simulated dew formation.Transpiration of urban trees and its cooling effect in a high latitude city.Blue light dose-responses of leaf photosynthesis, morphology, and chemical composition of Cucumis sativus grown under different combinations of red and blue lightSmaller, faster stomata: scaling of stomatal size, rate of response, and stomatal conductance.Aquaporins and leaf hydraulics: poplar sheds new light.Species Introductions and Their Cascading Impacts on Biotic Interactions in desert riparian ecosystems.Physiological acclimation dampens initial effects of elevated temperature and atmospheric CO2 concentration in mature boreal Norway spruce.Pre-dawn stomatal opening does not substantially enhance early-morning photosynthesis in Helianthus annuus.Measurement and interpretation of the oxygen isotope composition of carbon dioxide respired by leaves in the dark.Fog reduces transpiration in tree species of the Canarian relict heath-laurel cloud forest (Garajonay National Park, Spain).Depressed hydraulic redistribution of roots more by stem refilling than by nocturnal transpiration for Populus euphratica Oliv. in situ measurement.Biotic- and abiotic-driven variations of the night-time sap flux of three co-occurring tree species in a low subtropical secondary broadleaf forest.Comparative study of diurnal and nocturnal sap flow of Quercus ilex and Phillyrea latifolia in a Mediterranean holm oak forest in Prades (Catalonia, NE Spain)Helianthus nighttime conductance and transpiration respond to soil water but not nutrient availability
P2860
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P2860
Night-time conductance in C3 and C4 species: do plants lose water at night?
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh-hant
name
Night-time conductance in C3 and C4 species: do plants lose water at night?
@en
Night-time conductance in C3 and C4 species: do plants lose water at night?
@nl
type
label
Night-time conductance in C3 and C4 species: do plants lose water at night?
@en
Night-time conductance in C3 and C4 species: do plants lose water at night?
@nl
prefLabel
Night-time conductance in C3 and C4 species: do plants lose water at night?
@en
Night-time conductance in C3 and C4 species: do plants lose water at night?
@nl
P356
P1476
Night-time conductance in C3 and C4 species: do plants lose water at night?
@en
P2093
Richards JH
P304
P356
10.1093/JXB/ERG082
P577
2003-02-01T00:00:00Z